SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12751558 | snp | A/T | 0.272511 | 0.248984 | intron-variant | VAV3 | GRCh38.p7 | 1:107728453 | ATTTGAGGGAAAAAT[A/T]ATCTGTTAATTGATC | 10451 |
rs12751906 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107721376 | ATAACATGGCCAATA[A/C]CCTTTATCAAGGTCT | 10451 |
rs12751945 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | VAV3 | GRCh38.p7 | 1:107751512 | ACGGTTCGGCAATTA[A/G]TATTTTTTGAGCATC | 10451 |
rs12752530 | snp | A/C | 0.455263 | 0.142713 | intron-variant | VAV3 | GRCh38.p7 | 1:107633960 | accaccttatcaccc[A/C]tagcattatgagaaa | 10451 |
rs12754011 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | VAV3 | GRCh38.p7 | 1:107783931 | caggcatggtggcgg[A/G]cacctgtagtcccag | 10451 |
rs12754339 | snp | C/T | 0.131381 | 0.220067 | intron-variant | VAV3 | GRCh38.p7 | 1:107783447 | GAATAGTAGCTGATG[C/T]TCTGTGAGGGCTAAG | 10451 |
rs12754417 | snp | A/C | 0.127599 | 0.217986 | intron-variant | VAV3 | GRCh38.p7 | 1:107790726 | AGAGTCTTGCTTTGT[A/C]ACCAAGGCTGGAGTA | 10451 |
rs12754651 | snp | C/T | 0.131381 | 0.220067 | intron-variant | VAV3 | GRCh38.p7 | 1:107783627 | CTGAACCCAGTGAGG[C/T]CACCCACTCCTCCAC | 10451 |
rs12756561 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701319 | tgaagcaaaggcctg[A/G]ggcttgcaccctctg | 10451 |
rs12757545 | snp | C/T | 0.479421 | 0.0993283 | intron-variant | VAV3 | GRCh38.p7 | 1:107650723 | CCCCTCCCCCCACCC[C/T]ACAACAGTCCCAGAG | 10451 |
rs12758917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599255 | CTACATGTTTCTAAC[C/T]GGGTAGAACTAAATA | 10451 |
rs13353016 | snp | C/T | 0.150333 | 0.229274 | intron-variant | VAV3 | GRCh38.p7 | 1:107856873 | gagacctcatctcta[C/T]aaaaacttttaaaat | 10451 |
rs13373947 | snp | A/G | 0.159622 | 0.233092 | intron-variant | VAV3 | GRCh38.p7 | 1:107855772 | GCCTAATAACAAAGC[A/G]GCCAGGGGGAATAAA | 10451 |
rs13374031 | snp | C/T | 0.206336 | 0.246157 | intron-variant | VAV3 | GRCh38.p7 | 1:107856033 | CAACAGAAGCACAGC[C/T]GGGCATGTTCTGAGT | 10451 |
rs13374240 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107857441 | tatattctattCTTA[C/T]TAAAAATCCTAAGTT | 10451 |
rs13374390 | snp | C/T | 0.43655 | 0.16643 | intron-variant | VAV3 | GRCh38.p7 | 1:107728606 | ATACGTATACGTATA[C/T]GTATATGTATATGTA | 10451 |
rs13374478 | snp | C/T | 0.339429 | 0.233457 | intron-variant | VAV3 | GRCh38.p7 | 1:107784718 | CCATCACCTAGTTCA[C/T]AGACAGGCTCACAGC | 10451 |
rs13375446 | snp | C/T | 0.278133 | 0.248412 | intron-variant | VAV3 | GRCh38.p7 | 1:107754601 | ATAGAAACCTTTTAA[C/T]AGCTTCCCACTGCAG | 10451 |
rs13375688 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107819444 | tgggaggctgaaggt[A/G]ggagaattgccttgg | 10451 |
rs13375692 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107819502 | acataacaagactct[A/G]tctcaaaaaaaaaaa | 10451 |
rs13375984 | snp | C/T | 0.26518 | 0.249539 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965542 | AATGAAAAAAGTGCC[C/T]AGAGCATCAGTAGAG | 10451 |
rs13376677 | snp | A/G | 0.343924 | 0.231686 | intron-variant | VAV3 | GRCh38.p7 | 1:107784645 | TTGGTCTTTCAATCT[A/G]ACAACGGAAAATTTC | 10451 |
rs17014208 | snp | C/T | 0.220246 | 0.248223 | intron-variant | VAV3 | GRCh38.p7 | 1:107795876 | AAAGTGCTGAGCTTA[C/T]TAGAAAGTAATGGAC | 10451 |
rs17019453 | snp | C/T | 0.0614824 | 0.164198 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572462 | TAAAATGACATAAAT[C/T]ATAGCCCTTGATCTG | 10451 |
rs17019458 | snp | A/T | 0.00914312 | 0.0669923 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573146 | TCTAGGCAAGCCATT[A/T]ATCTGTCAGTACCAG | 10451 |
rs17019474 | snp | C/T | 0.299411 | 0.245069 | intron-variant | VAV3 | GRCh38.p7 | 1:107585936 | CACACAAGTGGCCTG[C/T]TAGAAAGAAGTGCTT | 10451 |
rs17019483 | snp | A/C/T | 0.0898077 | 0.191933 | intron-variant | VAV3 | GRCh38.p7 | 1:107596150 | GGAAGGAAGATGTTT[A/C/T]ATGTTATTGTGCCCC | 10451 |
rs17019498 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | VAV3 | GRCh38.p7 | 1:107599358 | AGTCATTGACCTTCA[C/G]GTACAACAAGTAAAT | 10451 |
rs17019501 | snp | G/T | 0.440746 | 0.161604 | intron-variant | VAV3 | GRCh38.p7 | 1:107599909 | ATAATAGACAAGTGT[G/T]TTATTTGACTCCAAC | 10451 |
rs17019507 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107601018 | AAGCTCAAGCTGGTA[C/T]GTCTTGCAGAGATGT | 10451 |
rs17019522 | snp | C/T | 0.440884 | 0.161442 | intron-variant | VAV3 | GRCh38.p7 | 1:107603608 | TCTAGCAATAAGTTA[C/T]TTTAAATAGTTTTTT | 10451 |
rs17019524 | snp | C/T | 0.441021 | 0.161279 | intron-variant | VAV3 | GRCh38.p7 | 1:107604663 | ATACCATCTAAAGAA[C/T]GTTGTCCTGCATCTT | 10451 |
rs17019580 | snp | C/T | 0.283684 | 0.24772 | intron-variant | VAV3 | GRCh38.p7 | 1:107641225 | TTCAATCTTTGGGCA[C/T]TCTTATATAACAAGA | 10451 |
rs17019588 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107641756 | CCCCTGAAGTGAACT[C/G]TTAATATATTAAAGC | 10451 |
rs17019596 | snp | C/T | 0.482683 | 0.0914256 | intron-variant | VAV3 | GRCh38.p7 | 1:107644891 | AAATTATATTTAACA[C/T]TACAAAGGGTACATA | 10451 |
rs17019599 | snp | C/G | 0.482609 | 0.0916147 | intron-variant | VAV3 | GRCh38.p7 | 1:107645121 | CCTAGTAGCACACTA[C/G]TATAGGTATGTTGCT | 10451 |
rs17019602 | snp | A/G | 0.317933 | 0.240593 | intron-variant | VAV3 | GRCh38.p7 | 1:107646236 | CATATTCCTTAAAAA[A/G]TGACAAGAAATACAC | 10451 |
rs17019614 | snp | A/G | 0.278664 | 0.248351 | intron-variant | VAV3 | GRCh38.p7 | 1:107648014 | AGTAAAAGGAACCAC[A/G]GCATAGAATTTTGGT | 10451 |
rs17019623 | snp | A/G | 0.370974 | 0.218781 | intron-variant | VAV3 | GRCh38.p7 | 1:107654724 | CCAAAATTATATTAT[A/G]GTTTTCACTTATTCA | 10451 |
rs17019630 | snp | A/G | 0.112631 | 0.208878 | intron-variant | VAV3 | GRCh38.p7 | 1:107657345 | TATAAAGGGGACTTT[A/G]TAAGAAAATTCCACA | 10451 |
rs17019693 | snp | C/T | 0.309894 | 0.242719 | intron-variant | VAV3 | GRCh38.p7 | 1:107672688 | TAATTTAGAAAAGCA[C/T]CAAATCTTGAATAGA | 10451 |
rs17019729 | snp | C/T | 0.267364 | 0.249396 | intron-variant | VAV3 | GRCh38.p7 | 1:107703042 | TCTAAACTATTCTCC[C/T]ACACTATTTCCTTTA | 10451 |
rs17019743 | snp | C/G | 0.235273 | 0.249566 | intron-variant | VAV3 | GRCh38.p7 | 1:107706557 | CATTTTTGTGTTACT[C/G]ATTAAAAATTGCAGA | 10451 |
rs17019768 | snp | C/G | 0.214843 | 0.247516 | intron-variant | VAV3 | GRCh38.p7 | 1:107720934 | GATAAGGTATGAGAG[C/G]ATAATTGGCTATCCT | 10451 |
rs17019773 | snp | C/T | 0.235273 | 0.249566 | intron-variant | VAV3 | GRCh38.p7 | 1:107721390 | AACCTTTATCAAGGT[C/T]TAGGACTTCTGAGAC | 10451 |
rs17019776 | snp | A/G | 0.207559 | 0.246371 | intron-variant | VAV3 | GRCh38.p7 | 1:107721526 | ATACAGAAGAAAATG[A/G]GTGCTTGTAGAGGCA | 10451 |
rs17019787 | snp | C/G | 0.234692 | 0.249531 | intron-variant | VAV3 | GRCh38.p7 | 1:107723344 | CCTTCTGTGTTTTCT[C/G]TCCACACAAATTCAC | 10451 |
rs17019789 | snp | A/G | 0.207559 | 0.246371 | intron-variant | VAV3 | GRCh38.p7 | 1:107723911 | CATTGGATAAATAGA[A/G]AACACATCGTAAATG | 10451 |
rs17019790 | snp | C/T | 0.234692 | 0.249531 | intron-variant | VAV3 | GRCh38.p7 | 1:107723977 | CATTTTTTTCATTTC[C/T]AAATTGAAGCTCAGA | 10451 |
rs17019795 | snp | C/T | 0.234109 | 0.249494 | intron-variant | VAV3 | GRCh38.p7 | 1:107724348 | GTATAATGATCTGTC[C/T]TTTCTCTGAAGTTAT | 10451 |
rs17019798 | snp | A/G | 0.234401 | 0.249513 | intron-variant | VAV3 | GRCh38.p7 | 1:107724593 | GATATGGTGGAGAAT[A/G]AAAGAGAGATTGGAC | 10451 |
rs17019802 | snp | A/G | 0.41833 | 0.184838 | intron-variant | VAV3 | GRCh38.p7 | 1:107725110 | GGAGTGAATAAAGGA[A/G]TCAGAAATGATAAAA | 10451 |
rs17019810 | snp | C/T | 0.227664 | 0.249 | intron-variant | VAV3 | GRCh38.p7 | 1:107726179 | CTGATATTTGCAAAG[C/T]ACTTTTGGTTCAGAC | 10451 |
rs17019823 | snp | A/C | 0.227074 | 0.248947 | intron-variant | VAV3 | GRCh38.p7 | 1:107727331 | CCTATTCTGTTTTTA[A/C]GATGATGAATATGAT | 10451 |
rs17019828 | snp | C/T | 0.148996 | 0.228688 | intron-variant | VAV3 | GRCh38.p7 | 1:107727508 | ATGAAATCAGGTTTA[C/T]TGGCAATTTTAAATA | 10451 |
rs17019840 | snp | A/G | 0.152667 | 0.230274 | intron-variant | VAV3 | GRCh38.p7 | 1:107728812 | ACAATAATGCAAGCC[A/G]AGGGCGCAACTATAG | 10451 |
rs17019843 | snp | A/T | 0.214239 | 0.247429 | intron-variant | VAV3 | GRCh38.p7 | 1:107730651 | GATGGTTGTTAATAA[A/T]ATACACAATGTTACT | 10451 |
rs17019844 | snp | A/G | 0.207559 | 0.246371 | intron-variant | VAV3 | GRCh38.p7 | 1:107730781 | GAATGAATATGCTAC[A/G]CAGGAATACCTCTTG | 10451 |
rs17019845 | snp | C/G | 0.211516 | 0.24702 | intron-variant | VAV3 | GRCh38.p7 | 1:107731203 | TGCACAATTCAATCA[C/G]AAGTCTCCAAACTGA | 10451 |
rs17019846 | snp | A/G | 0.21303 | 0.247251 | intron-variant | VAV3 | GRCh38.p7 | 1:107732010 | TTACTTCTAAGTGAA[A/G]AGAAAAAATATTTGG | 10451 |
rs17019855 | snp | A/G | 0.435119 | 0.16802 | intron-variant | VAV3 | GRCh38.p7 | 1:107742766 | GAGAAGTAAAACTGA[A/G]ACGACCTCAGATTCT | 10451 |
rs17019880 | snp | C/T | 0.199254 | 0.244796 | intron-variant | VAV3 | GRCh38.p7 | 1:107745598 | TGGGGAGAATATTTA[C/T]GTTCACCAGATACTT | 10451 |
rs17019881 | snp | C/G | 0.207864 | 0.246424 | intron-variant | VAV3 | GRCh38.p7 | 1:107747241 | TGAACAAAATAGTAA[C/G]TGACATGCCTGTCAT | 10451 |
rs17019888 | snp | C/T | 0.269809 | 0.249214 | intron-variant | VAV3 | GRCh38.p7 | 1:107747630 | CTGTAGCTGCTATTG[C/T]ACTATTTGGCTAGCT | 10451 |
rs17019891 | snp | C/T | 0.270351 | 0.24917 | intron-variant | VAV3 | GRCh38.p7 | 1:107748431 | GAGCTTCCTCCTCAG[C/T]GGAACTAAAAGCCAC | 10451 |
rs17019893 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107748891 | ACAAGCATTAGAGTA[C/G]ACTTATTGGTTGTTC | 10451 |
rs17019913 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107761936 | CTCTTCTTTCCTAAA[C/G]GTTTATTTTAAAATA | 10451 |
rs17019964 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107765870 | TAATTCATTAGCCAC[G/T]TCTTAGTACTAGGAA | 10451 |
rs17019985 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107771773 | GGACTGCCCTTGCGG[A/G]AGACAGTGAAGAATG | 10451 |
rs17020006 | snp | A/G | 0.0122311 | 0.0772394 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107777269 | GTAGATGTCTTCATC[A/G]TTAATGCTTTCTTCT | 10451 |
rs17020010 | snp | C/T | 0.228253 | 0.249052 | intron-variant | VAV3 | GRCh38.p7 | 1:107778780 | GTAGAGACTGTTTTG[C/T]TTTATTTCCTAATGT | 10451 |
rs17020011 | snp | C/T | 0.228253 | 0.249052 | intron-variant | VAV3 | GRCh38.p7 | 1:107778919 | CATAATACTCTATTG[C/T]AAGGAGATGACATAC | 10451 |
rs17020012 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107780311 | TTAATTTAATTCTGA[C/G]TGTTTTCAGAAAAAG | 10451 |
rs17020022 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107782741 | TGTATTCTATAAAGG[C/T]GAAGCGTATCCGGAT | 10451 |
rs17020031 | snp | A/G | 0.0349115 | 0.127424 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786293 | GAATCTTCAAAAGTG[A/G]AACTACAGAGAACAA | 10451 |
rs17020047 | snp | C/T | 0.226779 | 0.248919 | intron-variant | VAV3 | GRCh38.p7 | 1:107789448 | GCTCAAAGAAAATCA[C/T]GAAGCATCTGTAAAC | 10451 |
rs17020055 | snp | A/C | 0.270892 | 0.249126 | intron-variant | VAV3 | GRCh38.p7 | 1:107793911 | GACAAGCATTATGAA[A/C]ACAGGGATCCACTTG | 10451 |
rs17020064 | snp | C/T | 0.226779 | 0.248919 | intron-variant | VAV3 | GRCh38.p7 | 1:107795178 | CTTGTTCTCATCTGC[C/T]AAGCTGATTTTCCTC | 10451 |
rs17020067 | snp | C/T | 0.423726 | 0.179776 | intron-variant | VAV3 | GRCh38.p7 | 1:107796722 | AATTCCTGGGAATCA[C/T]GACAGAGTCAATAAG | 10451 |
rs17020078 | snp | G/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107806611 | ATACCAATATTTTTA[G/T]TGTAAATCCTCTATA | 10451 |
rs17020080 | snp | C/G | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107806657 | CAATCCTAACCACCA[C/G]TTTTCTTCAAATGAG | 10451 |
rs17020081 | snp | A/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107807230 | AACCCTTTCCTCGTG[A/T]TCCTTTGTCAAATAT | 10451 |
rs17020085 | snp | C/T | 0.218151 | 0.247963 | intron-variant | VAV3 | GRCh38.p7 | 1:107809007 | TCCCTAGAAATAAGC[C/T]ATTCTAAACTATTCA | 10451 |
rs17020086 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107809179 | AAATAAGCAAAGCCT[C/T]ATCATTTCTTTCTTT | 10451 |
rs17020088 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107809190 | GCCTCATCATTTCTT[C/T]CTTTGGACTACTTTT | 10451 |
rs17020100 | snp | G/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107810229 | CACTACAGAGGTGGG[G/T]TGTCACTCAGGCATT | 10451 |
rs17020103 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107810405 | AAAGTGAAGTTCTTG[C/T]CCAGGGAACTGAGCA | 10451 |
rs17020104 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107811048 | CTTTCAGAAGTCCTT[C/T]CTCTACTCATGAAGG | 10451 |
rs17020105 | snp | A/C | 0.320575 | 0.239832 | intron-variant | VAV3 | GRCh38.p7 | 1:107811106 | TCCTTCTAAAACAGA[A/C]ACAGAAGGCACAGAG | 10451 |
rs17020107 | snp | C/T | 0.32153 | 0.239548 | intron-variant | VAV3 | GRCh38.p7 | 1:107811226 | TAGAAGTTGAACAGG[C/T]ATCTTTTAGAGAGGA | 10451 |
rs17020108 | snp | A/T | 0.32153 | 0.239548 | intron-variant | VAV3 | GRCh38.p7 | 1:107811339 | GATCTGCACAGGGTA[A/T]GATACTGGGCATGAC | 10451 |
rs17020110 | snp | C/T | 0.440057 | 0.162414 | intron-variant | VAV3 | GRCh38.p7 | 1:107811534 | TCACATTTTTAAAAT[C/T]AATTATTTCCTTACC | 10451 |
rs17020112 | snp | A/C | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107811677 | AACTATTATATAGCA[A/C]CATAATAAACAAAAG | 10451 |
rs17020122 | snp | C/T | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107814769 | GAGGTATGATGAAAA[C/T]AGTGCTTATGGAAGA | 10451 |
rs17020123 | snp | A/G | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107814951 | GCCTGATTTATAAGC[A/G]TCAATAGAACTTGGT | 10451 |
rs17020124 | snp | A/G | 0.229136 | 0.249128 | intron-variant | VAV3 | GRCh38.p7 | 1:107815389 | TCAGAGTTCCAGAGT[A/G]GAGGCTGAAGTACAG | 10451 |
rs17020127 | snp | A/G | 0.227664 | 0.249 | intron-variant | VAV3 | GRCh38.p7 | 1:107815461 | TCATCACCAAATTCA[A/G]TGATGTGATTTTACG | 10451 |
rs17020137 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107826269 | GGAAAAGAATCATTT[A/G]CTCCATTACGCTACT | 10451 |
rs17020139 | snp | A/G | 0.226779 | 0.248919 | intron-variant | VAV3 | GRCh38.p7 | 1:107826861 | GTGTAATGTCAGCCC[A/G]AGTCTATATTTTTTA | 10451 |
rs17020141 | snp | A/G | 0.226779 | 0.248919 | intron-variant | VAV3 | GRCh38.p7 | 1:107827250 | TTAAGGAATGGAAAG[A/G]ACAGCACTATTTGAC | 10451 |
rs17020144 | snp | A/G | 0.030278 | 0.119257 | intron-variant | VAV3 | GRCh38.p7 | 1:107828265 | TTCTGCCTTTCAAGC[A/G]TACAAGATTCAGTGA | 10451 |
rs17020146 | snp | A/C | 0.229136 | 0.249128 | intron-variant | VAV3 | GRCh38.p7 | 1:107832080 | ATCCAGGTGTGAAGT[A/C]AAGTCAGTCTCATCT | 10451 |
rs17020148 | snp | C/G | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107832388 | ACAATGATAAGAACA[C/G]GAAGAACCTTCGAAA | 10451 |
rs17020149 | snp | A/G | 0.227664 | 0.249 | intron-variant | VAV3 | GRCh38.p7 | 1:107832667 | TGTCTTTAACACCTC[A/G]GTAGAAATGGCTCCC | 10451 |
rs17020150 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107833872 | CAAGTTCTTCCTTGA[C/T]TACTACAAGTAATCA | 10451 |
rs17020151 | snp | C/G | 0.120674 | 0.21395 | intron-variant | VAV3 | GRCh38.p7 | 1:107834082 | AAAGCAGAACCAGGT[C/G]TTTTAACTACAGTCA | 10451 |
rs17020160 | snp | C/T | 0.186105 | 0.241697 | intron-variant | VAV3 | GRCh38.p7 | 1:107841366 | ATATGGGGAAAAAAA[C/T]TAAAGCAATATAAAG | 10451 |
rs17020163 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | VAV3 | GRCh38.p7 | 1:107842211 | CTCTTCTTTAAGACA[C/T]TGCTTTAAACATTTA | 10451 |
rs17020175 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | VAV3 | GRCh38.p7 | 1:107853034 | TTTTTGCCATCATTT[C/T]CAACAGGTTTGAAAG | 10451 |
rs17020181 | snp | C/T | 0.224709 | 0.248717 | intron-variant | VAV3 | GRCh38.p7 | 1:107853340 | ATCTATGCTGCAACA[C/T]AGGAGACAAGTGTTT | 10451 |
rs17020184 | snp | A/T | 0.223522 | 0.248594 | intron-variant | VAV3 | GRCh38.p7 | 1:107854484 | CCACAAATTTTGCAA[A/T]CTTATGATTATGTTG | 10451 |
rs17020234 | snp | C/T | 0.17332 | 0.23795 | intron-variant | VAV3 | GRCh38.p7 | 1:107872717 | ATGTGAATGTTTGCA[C/T]TATGGTACAGTAGTG | 10451 |
rs17020245 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | VAV3 | GRCh38.p7 | 1:107881831 | CTTTTCAAGGTGCAG[A/C]CTCCTGTTACCACTT | 10451 |
rs17020273 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | VAV3 | GRCh38.p7 | 1:107887673 | TTCTAAACCCTTGGT[C/T]ACTGTTCACAGAAAG | 10451 |
rs17020274 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | VAV3 | GRCh38.p7 | 1:107888191 | TGATATCTTCTTTAT[C/T]GAAAGAGGTAATCTG | 10451 |
rs17020276 | snp | C/T | 0.119978 | 0.213528 | intron-variant | VAV3 | GRCh38.p7 | 1:107894467 | TTAAAACAAGCTGAA[C/T]TCTCATAATAAGGAA | 10451 |
rs17020294 | snp | C/T | 0.345925 | 0.230864 | intron-variant | VAV3 | GRCh38.p7 | 1:107899020 | AAGCTTACTATACAT[C/T]AGAAAAACAAACAAA | 10451 |
rs17020298 | snp | G/T | 0.0711525 | 0.174681 | intron-variant | VAV3 | GRCh38.p7 | 1:107899424 | TTCAACGACCTTACA[G/T]CCCACTAGCAAAGAG | 10451 |
rs17020319 | snp | G/T | 0.0711525 | 0.174681 | intron-variant | VAV3 | GRCh38.p7 | 1:107902648 | TGAGGTCCTACATGT[G/T]TAAACCTTTAAGAAA | 10451 |
rs17020332 | snp | C/G | 0.110519 | 0.207473 | intron-variant | VAV3 | GRCh38.p7 | 1:107909766 | TAATGCAGGTATCCA[C/G]ACTCTGCCATGTATA | 10451 |
rs17020334 | snp | C/T | 0.239326 | 0.249772 | intron-variant | VAV3 | GRCh38.p7 | 1:107911185 | TACGAAAAGAGTATT[C/T]CCAAGCTTCTAAAAG | 10451 |
rs17020336 | snp | G/T | 0.239614 | 0.249784 | intron-variant | VAV3 | GRCh38.p7 | 1:107911266 | TTACTAACATTAACA[G/T]GTATATATCTGTGTA | 10451 |
rs17020361 | snp | A/G | 0.112631 | 0.208878 | intron-variant | VAV3 | GRCh38.p7 | 1:107917213 | AGAACCTGTACTCAA[A/G]CATCAGCAGCGGCCT | 10451 |
rs17020373 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | VAV3 | GRCh38.p7 | 1:107919128 | CAATGACTTGAAATA[C/T]ACTCAATAGTTATTC | 10451 |
rs17020384 | snp | C/G | 0.110872 | 0.20771 | intron-variant | VAV3 | GRCh38.p7 | 1:107921906 | TTCCTTGCTATTACA[C/G]TAGTTCATGGAGGAT | 10451 |
rs17020387 | snp | C/T | 0.191461 | 0.24305 | intron-variant | VAV3 | GRCh38.p7 | 1:107932019 | ACCAGCATAGCACAA[C/T]GATAGCTCTCACACC | 10451 |
rs17020390 | snp | A/G | 0.192088 | 0.2432 | intron-variant | VAV3 | GRCh38.p7 | 1:107934129 | TCAAAAGTGCCTTCT[A/G]TTCTTATTATCTTGG | 10451 |
rs17020392 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107934248 | AAATATTGCAAAACC[C/T]AAGACTTTCCTGGAT | 10451 |
rs17020395 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107934802 | ACACACTCTGGGGAA[G/T]TTTGTGAATCACTGT | 10451 |
rs17020400 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | VAV3 | GRCh38.p7 | 1:107934911 | AAACAAATTCTTGCA[C/T]GACCAGGCTATCTGC | 10451 |
rs17020405 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | VAV3 | GRCh38.p7 | 1:107934948 | GAGGAGAAGAGTTGG[C/T]AGTACATGAACCCAT | 10451 |
rs17020409 | snp | C/T | 0.111224 | 0.207945 | intron-variant | VAV3 | GRCh38.p7 | 1:107935183 | GCTGTAAGATTACAG[C/T]TTCCTACAGTTCTCC | 10451 |
rs17020424 | snp | C/T | 0.185155 | 0.241444 | intron-variant | VAV3 | GRCh38.p7 | 1:107938217 | AGAGGAGGCGATCCC[C/T]GAGCCAGAAAACAGG | 10451 |
rs17020428 | snp | C/T | 0.111224 | 0.207945 | intron-variant | VAV3 | GRCh38.p7 | 1:107938367 | GAGGCAGGAGTGTCT[C/T]AGGGATCTAGATTCT | 10451 |
rs17020437 | snp | C/T | 0.111224 | 0.207945 | intron-variant | VAV3 | GRCh38.p7 | 1:107941495 | TTGATTCCAGAACCA[C/T]TTCCGAGGCCAACAT | 10451 |
rs17229521 | snp | G/T | 0.265453 | 0.249522 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966821 | TTTCTAGGCCATAAT[G/T]TTGGCAAATAAATCA | 10451 |
rs17229543 | in-del | -/CAAA | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966515 | CAAAAAACAAACAAA[-/CAAA]CAAACAAAAAGATGG | 10451 |
rs17229564 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787320 | AGGAAGCATTGTATC[C/T]TCATTTTGCTCCCTG | 10451 |
rs17229578 | snp | A/G | 0.0667028 | 0.170006 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107785974 | ATTAGGATACACTAC[A/G]GCTTAGTGTCACTTC | 10451 |
rs17229585 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107785266 | AAGAAAGGCACAGCC[A/G]CAGTAACCAGAGGAA | 10451 |
rs17229592 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | VAV3 | GRCh38.p7 | 1:107785176 | TTACAAATAACATCA[A/G]CAGCACTAATGTGCT | 10451 |
rs17229633 | snp | A/G | 0.00220745 | 0.0331489 | intron-variant | VAV3 | GRCh38.p7 | 1:107751222 | ATGAAAAACTCTGAC[A/G]TGTGCATTTTATATT | 10451 |
rs17229647 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107749391 | AAAGTATGATAATAC[A/G]TTAATGTGAGATATG | 10451 |
rs17229654 | snp | C/T | 0.00260283 | 0.0359811 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749073 | AATTTTAACAGTGGT[C/T]TTATGGCTTCTACCT | 10451 |
rs17229661 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | VAV3 | GRCh38.p7 | 1:107688068 | GGTAGATGCGTCCCC[A/G]TCATGAAATGTTGTG | 10451 |
rs17229668 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107688033 | TGCCCGACATTTGCC[A/G]AATTACTGAAATTCC | 10451 |
rs17229691 | in-del | -/GGGGGTA | 0.02016 | 0.0983543 | intron-variant | VAV3 | GRCh38.p7 | 1:107596563 | CTGTGAATAACAATA[-/GGGGGTA]ACTCATATTATTAAT | 10451 |
rs17229705 | snp | A/G | 0.0962521 | 0.197133 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107596339 | CTTTTTTCCAAAGGA[A/G]CTTGTGGAGTACTAC | 10451 |
rs17235920 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966476 | ACTGCACTCCAGCCT[A/G]GACGACAGAGCCAGA | 10451 |
rs17235934 | in-del | -/GTGT | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964365 | CTTCACCTACTCTGC[-/GTGT]GTGTGGCGCGACAAA | 10451 |
rs17235955 | snp | C/T | 0.340333 | 0.233109 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786930 | ATAGCTTTCATCATA[C/T]TCTCAAAGGGATCTA | 10451 |
rs17235962 | snp | A/T | 0.0670745 | 0.170406 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786771 | CTACTCCAAATAAAC[A/T]CAAAAATCTGTGTAA | 10451 |
rs17235983 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | VAV3 | GRCh38.p7 | 1:107777682 | CTGAAAAGAGAGGGT[A/G]CTGAAGGCAAGGGTA | 10451 |
rs17235990 | snp | C/G | 0.0248101 | 0.10858 | intron-variant | VAV3 | GRCh38.p7 | 1:107777343 | TGATTGTTGCTCGTT[C/G]ACTCATGGGTTTGTT | 10451 |
rs17235997 | snp | C/T | 0.00188118 | 0.0306113 | intron-variant | VAV3 | GRCh38.p7 | 1:107777312 | TTTTTGTTTTTGTTT[C/T]TTCTCCTCTTCCTAG | 10451 |
rs17236011 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755286 | CCTCAGACACCCACA[C/T]GAACACTGCCAAACA | 10451 |
rs17236050 | snp | C/T | 0.460365 | 0.13508 | intron-variant | VAV3 | GRCh38.p7 | 1:107690604 | GGAAGCAGGAGACAA[C/T]GACAAGGGAGGAAAT | 10451 |
rs17236064 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107642283 | GTGAGGACGACCAGA[A/G]GTCACTTGGTTTTGG | 10451 |
rs17236099 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | VAV3 | GRCh38.p7 | 1:107573429 | TCTGACACTTCAAAG[A/G]ATTCTACAAACAGAG | 10451 |
rs17236113 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572685 | TATAATCAGGACACC[A/G]AATAAGTAATTAAAA | 10451 |
rs17236120 | snp | C/T | 0.0119091 | 0.0762411 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571722 | TATTTGCTAAAACCA[C/T]TTAAGTCTTTGTATA | 10451 |
rs17477236 | snp | A/C | 0.24449 | 0.249939 | intron-variant | VAV3 | GRCh38.p7 | 1:107581858 | GGAAACCAACCTAAT[A/C]GACACTCTTCGTTCA | 10451 |
rs17477334 | snp | A/T | 0.178144 | 0.239451 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593644 | TGCACAATCTTTCTA[A/T]ACAAACATGCAGCAT | 10451 |
rs17479238 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | VAV3 | GRCh38.p7 | 1:107648809 | TCCCTACTTCAGGTT[C/G]GTCATTCTATGCAAC | 10451 |
rs17479259 | snp | C/T | 0.176861 | 0.239062 | intron-variant | VAV3 | GRCh38.p7 | 1:107648891 | TGTTTCAGGATGATC[C/T]GAGTACCCGCCACAT | 10451 |
rs17479604 | snp | A/C | 0.233235 | 0.249437 | intron-variant | VAV3 | GRCh38.p7 | 1:107661025 | ATCTATATACACACA[A/C]ACATAAAGAAGTACA | 10451 |
rs17481300 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107713673 | ACACTGAAGGGTTTT[C/T]ATAAAAGGGAAATTG | 10451 |
rs17482100 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107731859 | TGAAGATTTTGACCA[C/T]TATGAAAAGGTATTC | 10451 |
rs17482377 | snp | A/C | 0.0825414 | 0.185628 | intron-variant | VAV3 | GRCh38.p7 | 1:107745008 | AAAAATTCATAAAAG[A/C]ACAATGGATATATTG | 10451 |
rs17483780 | snp | C/T | 0.132066 | 0.220435 | intron-variant | VAV3 | GRCh38.p7 | 1:107772190 | AATGTTCTGGATATA[C/T]TAATAGCAGATAAGG | 10451 |
rs17483855 | snp | A/G | 0.340333 | 0.233109 | intron-variant | VAV3 | GRCh38.p7 | 1:107773324 | ATATTTCAAGACCTC[A/G]GTTTCATCAACTGTA | 10451 |
rs17483925 | snp | A/G | 0.131381 | 0.220067 | intron-variant | VAV3 | GRCh38.p7 | 1:107773772 | TAGGGCAGGTAAATC[A/G]GTTTGCACATTCTCT | 10451 |
rs17484367 | snp | A/G | 0.21303 | 0.247251 | intron-variant | VAV3 | GRCh38.p7 | 1:107727031 | AAACATCATAACAAC[A/G]GTTGGGTAGAAATAA | 10451 |
rs17484794 | snp | A/G | 0.34437 | 0.231505 | intron-variant | VAV3 | GRCh38.p7 | 1:107792779 | TATCAAATTGAATAC[A/G]AAAGAAACAGTTAAC | 10451 |
rs17484815 | snp | C/T | 0.339429 | 0.233457 | intron-variant | VAV3 | GRCh38.p7 | 1:107793563 | ATCTGAACAAGGGAA[C/T]GGCTGAGTGGCAGAC | 10451 |
rs17484960 | snp | A/G | 0.493293 | 0.0575177 | intron-variant | VAV3 | GRCh38.p7 | 1:107794486 | ATTTTGATTTAAGAA[A/G]AAAGCTTAAGAATGA | 10451 |
rs17485868 | snp | A/G | 0.484561 | 0.0864924 | intron-variant | VAV3 | GRCh38.p7 | 1:107813378 | TATTGCCTCTTAGCA[A/G]CAAAGGGATCCAAAT | 10451 |
rs17536557 | snp | A/G | 0.180064 | 0.240019 | intron-variant | VAV3 | GRCh38.p7 | 1:107596903 | TCTGCTACTCACAGA[A/G]GTCAATGTAATTCTT | 10451 |
rs17538784 | snp | C/T | 0.173965 | 0.238157 | intron-variant | VAV3 | GRCh38.p7 | 1:107662944 | TGCACATCGACTTCT[C/T]GGGCTGCTCCAGGCT | 10451 |
rs17539492 | snp | G/T | 0.121022 | 0.21416 | intron-variant | VAV3 | GRCh38.p7 | 1:107679844 | CAAGTGTTATTTTCC[G/T]GATACCAACATCTGT | 10451 |
rs17539866 | snp | C/T | 0.133093 | 0.220981 | intron-variant | VAV3 | GRCh38.p7 | 1:107691839 | ACTCCATCTTTAATG[C/T]CAGCACAGAGTTCAA | 10451 |
rs17540379 | snp | A/G | 0.207559 | 0.246371 | intron-variant | VAV3 | GRCh38.p7 | 1:107710960 | AAACTAAAGATAATA[A/G]AAAACATATCTAATA | 10451 |
rs17541024 | snp | C/G | 0.423257 | 0.180228 | intron-variant | VAV3 | GRCh38.p7 | 1:107730510 | ATTAATCATATAAGG[C/G]TCAAAATCATATTAG | 10451 |
rs17541972 | snp | C/T | 0.0100571 | 0.0701955 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107757303 | ATTTGCCTTCTCAGT[C/T]GGATCAGTGGTATGT | 10451 |
rs17542174 | snp | C/G | 0.118933 | 0.212888 | intron-variant | VAV3 | GRCh38.p7 | 1:107758689 | CTATAATATAAATCA[C/G]ATCCTGTCTCTACCC | 10451 |
rs17542229 | snp | A/G | 0.127254 | 0.217792 | intron-variant | VAV3 | GRCh38.p7 | 1:107760132 | CACATACAGGTAGTA[A/G]ATCTTTTTAAAATGA | 10451 |
rs17542571 | snp | A/T | 0.132066 | 0.220435 | intron-variant | VAV3 | GRCh38.p7 | 1:107764704 | ACTAGTAAACATTTT[A/T]AATCTACATATACAT | 10451 |
rs17555966 | snp | A/G | 0.34101 | 0.232846 | intron-variant | VAV3 | GRCh38.p7 | 1:107780930 | GATAGTAAAAAGCGA[A/G]AAAAGGCAAAAATCT | 10451 |
rs17556001 | snp | C/T | 0.132066 | 0.220435 | intron-variant | VAV3 | GRCh38.p7 | 1:107781048 | AGAGTACCAGCCACA[C/T]ATACACTTATATCTC | 10451 |
rs17556028 | snp | C/T | 0.34101 | 0.232846 | intron-variant | VAV3 | GRCh38.p7 | 1:107781261 | CATGCCTATCATATG[C/T]TTAACTCAGTAAATG | 10451 |
rs17557345 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107810134 | TGCCACTGATTGGGT[A/T]AATCCTAGAGATACT | 10451 |
rs17557888 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107829544 | TCTGTGTGGGCACTT[C/T]CTTTGCACAGACCAC | 10451 |
rs17558834 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | VAV3 | GRCh38.p7 | 1:107880403 | TTCTCTGGACAAGAG[C/T]GCTGACAGAAGGAAC | 10451 |
rs28374986 | snp | A/T | 0.159951 | 0.233219 | intron-variant | VAV3 | GRCh38.p7 | 1:107822661 | CCATCTCAAAAAAAA[A/T]AAATAAATAAATAAA | 10451 |
rs28419482 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866113 | CAGCTTCTAAAGTCC[G/T]AGGATCAAGGTTAAA | 10451 |
rs28437539 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107818308 | TATCCACATGGAGCT[C/T]TACTGTGTTCCCTCA | 10451 |
rs28474380 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580972 | GTCCTGGAATAGAAT[A/T]AAAAAGGGCCCAGTA | 10451 |
rs28477098 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107890880 | AGAACTCTCTTCTCC[C/T]TAATTAGGTATTTAT | 10451 |
rs28490471 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107584229 | GCTGAAACTGGATCC[C/T]TTCCTTACACCTTAT | 10451 |
rs28505311 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933721 | CTCAGGAGGCTGAGG[G/T]GGGAGGATGGCTTGA | 10451 |
rs28631440 | snp | A/G | 0.232943 | 0.249417 | intron-variant | VAV3 | GRCh38.p7 | 1:107959091 | ACAAGGTAAAACCCC[A/G]TCTCTACTAAAATAC | 10451 |
rs28652575 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772211 | GCAGATAAGGTTTTG[A/G]GGGCTCATATTGGCT | 10451 |
rs28674923 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | VAV3 | GRCh38.p7 | 1:107835452 | CTCTGAACACTGAGA[A/G]GAGTGAGATGTGCGG | 10451 |
rs28675862 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918705 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 10451 |
rs28722699 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107879653 | CTGCCTTCAGAGATA[G/T]TTTATGAGTCAGAAG | 10451 |
rs28722824 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866114 | AGCTTCTAAAGTCCT[A/G]GGATCAAGGTTAAAC | 10451 |
rs33910884 | in-del | -/AAA/AT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107609551 | AAATAAAAAAAAAAA[-/AAA/AT]CTACTACTGTCCTTT | 10451 |
rs33976664 | in-del | -/TC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922296 | TGTCTTGTTTTGTGT[-/TC]CAGTATCCAGAAAAA | 10451 |
rs33983145 | in-del | -/A/AA/AAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933814 | AATGAGACCCTTCTC[-/A/AA/AAA]AAAAAAAAAAAAAAA | 10451 |
rs33993798 | in-del | -/GT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889133 | GTTCTCCTGTGTAGA[-/GT]GTGTGTGTGTGTGTG | 10451 |
rs34001682 | in-del | -/TGTT | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107798390 | TCCCAGGCAGGTGGC[-/TGTT]TGTGCCTCCAATAAG | 10451 |
rs34005895 | snp | A/T | 0.453087 | 0.145793 | intron-variant | VAV3 | GRCh38.p7 | 1:107851897 | TTTGCTGATTTTTTT[A/T]AAAAAGTTTTTCAAG | 10451 |
rs34005962 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107619244 | GGCTGCATCACTTGG[-/A]AAAAATGTAGAGAGA | 10451 |
rs34043686 | snp | A/G | 0.198324 | 0.244601 | intron-variant | VAV3 | GRCh38.p7 | 1:107802851 | TGATGTTAGCTTTGT[A/G]GAATAAGTTTGAAAG | 10451 |
rs34049721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107663484 | TTGGTAACTTTGGAT[C/T]GAAAATGAATATAAT | 10451 |
rs34058861 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107838156 | AAGTTCTAATAACCA[-/G]GAATCTATCAGGAAC | 10451 |
rs34062476 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107900500 | TACACCTTATAAAGT[-/G]CTAGACTTTGAGAAG | 10451 |
rs34108410 | in-del | -/T | 0.428333 | 0.175206 | intron-variant | VAV3 | GRCh38.p7 | 1:107764323 | ACCTAACTCAAATGC[-/T]GCCTCTTCAGATGAA | 10451 |
rs34114660 | in-del | -/GA | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107811904 | TAAATAATATGGCCT[-/GA]GAGATTTTGGTTTTA | 10451 |
rs34115881 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929234 | AGAGCTTGCAGTGAG[-/C]CCGAGATCACACCAC | 10451 |
rs34117734 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662764 | GGGCCTAATGGGTAG[-/A]AAAAAGACATATTAG | 10451 |
rs34120536 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710913 | TAAACTAGACATTAA[-/G]GGGATAGTTTCTTAC | 10451 |
rs34130275 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107691271 | GTTTCATTCTGGCTG[-/A]AAAAAATGGAATAAG | 10451 |
rs34142574 | in-del | -/C | | | intron-variant, utr-variant-5-prime | VAV3 | GRCh38.p7 | 1:107785516 | AGCCCCAAATGCAAG[-/C]ACGAGCTTGGGGGTT | 10451 |
rs34144151 | snp | C/T | 0.278664 | 0.248351 | intron-variant | VAV3 | GRCh38.p7 | 1:107584228 | AGCTGAAACTGGATC[C/T]CTTCCTTACACCTTA | 10451 |
rs34144387 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107573825 | AAGCTGTCCCACTTG[-/C]CCCAGGTGAATTTTA | 10451 |
rs34155119 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107818673 | TAAATAATAACACAT[-/G]GAATGTAAAACACAC | 10451 |
rs34155209 | in-del | -/C | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896315 | AAGTGGAGTGCCTCT[-/C]CCCCATCCCCACCCC | 10451 |
rs34180135 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929085 | GAAATTTTACAGGCC[-/A]TGAGGGAGTGACATG | 10451 |
rs34186959 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107830866 | TGTGAGCCACCGCAG[C/G]TGGCTTATAAAAATT | 10451 |
rs34215653 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107601216 | GCAGGGAGGATGCCT[-/G]GGATCTTGGTTACAA | 10451 |
rs34220497 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107646656 | CTTAATATATAACTT[-/G]GACAATTTTGCTCAT | 10451 |
rs34220918 | in-del | -/G | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895909 | CAGGAAATTACCCCT[-/G]GAAACAATTCAGCAG | 10451 |
rs34225175 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107901467 | TATCTTTGTGAAGCT[A/G]GATATTCAGCAGATG | 10451 |
rs34234160 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107813969 | TAAATAGTACTCCAG[-/T]GTGTGTGTGTGTGTG | 10451 |
rs34249858 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107848313 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs34255479 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753549 | ATATATATATATATA[C/T]ACACACACACACTTT | 10451 |
rs34256225 | snp | C/T | 0.455144 | 0.142885 | intron-variant | VAV3 | GRCh38.p7 | 1:107633886 | CCAATCCTGTGGACA[C/T]GGGCATTCGAGACCT | 10451 |
rs34265488 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632939 | TCTAATACTATACCA[-/G]GAAAATCTTCAAGTT | 10451 |
rs34280004 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107739821 | CATCCAGCTCATCCA[-/G]GGAAGGCTCCCCCTC | 10451 |
rs34284816 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621049 | ATAAATTGAACTGTT[-/G]CTGGGTAAACAAGTA | 10451 |
rs34291878 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941255 | CTTCTGAGTCCCATG[-/T]TTTCTAGTACTAAAG | 10451 |
rs34318889 | snp | C/T | 0.00308013 | 0.0391226 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107777262 | GGCCTTTGTAGATGT[C/T]TTCATCATTAATGCT | 10451 |
rs34338201 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107829253 | GCACTATTGTATTTT[-/A]AATCTGGGTTGACTC | 10451 |
rs34359829 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107752759 | ATGAGATATTGCTTT[-/A]AAAACCATTAAGATG | 10451 |
rs34368931 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107934690 | GAAACTCTTAGTTCC[-/A]AAAATAAGTTATGAT | 10451 |
rs34371003 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107861923 | CATACATACTTCAGT[-/G]GGGGAGTGTTCTGAA | 10451 |
rs34380131 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107788994 | TCCAGCAGAGTGGCT[-/G]GGGGATACAGCAGAC | 10451 |
rs34381784 | in-del | -/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107785646 | GAGCAAGTGCCCTGT[-/G]GGGGTTGTGGAGAAA | 10451 |
rs34387854 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107818652 | AGCTGGATTTTGTCA[-/T]TTTATGTAAATAATA | 10451 |
rs34392412 | snp | C/T | 0.00691947 | 0.0584111 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107705049 | GTCTGCATAGTCTGG[C/T]CTTATGTTAGACCTA | 10451 |
rs34400060 | snp | C/T | 0.2462 | 0.249971 | intron-variant | VAV3 | GRCh38.p7 | 1:107625352 | GCTCACTGCAACCTC[C/T]GCCTCCCGGGCTCAA | 10451 |
rs34416346 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107765273 | TTAAAACCATTGTTA[-/G]GGGATAACCAAAATA | 10451 |
rs34434455 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107769617 | TGTCAATTCAGTCTT[C/T]CCCCTTAATGCCTGA | 10451 |
rs34435766 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107851801 | ATATGAATCTACCCA[-/G]CTTAGAAAAATTTGT | 10451 |
rs34437461 | in-del | -/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757154 | ATATATGTGTGTATA[-/TG]TGTGTGTGTGTGTGT | 10451 |
rs34449160 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902477 | TATTTTTGGTACCAT[-/C]CCCCTGTTTTCTGCC | 10451 |
rs34454690 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107768769 | TGCTTCCAAAAGGAA[-/G]GGAAGAAAAGAACAT | 10451 |
rs34463672 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858052 | CTCTGGCAATAATAA[-/G]ATGTAATAAAGAATA | 10451 |
rs34479482 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107663213 | AACTTAAAAATATAC[-/T]TTTCCCTTTGCAGAT | 10451 |
rs34501550 | in-del | -/T | 0.375 | 0.216506 | intron-variant | VAV3 | GRCh38.p7 | 1:107771263 | TTTTTTTTTTTTTTT[-/T]GAGTCAGAGTCTCGC | 10451 |
rs34531609 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957997 | CTGCTTTCCAGAGAA[-/C]CTAGGTTAAGCCACC | 10451 |
rs34545058 | in-del | -/AT | 0.445987 | 0.155207 | intron-variant | VAV3 | GRCh38.p7 | 1:107784062 | AAGACCCTATCTCAA[-/AT]ATATATATATATATA | 10451 |
rs34560210 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107762117 | ACTATGGTGTTCTTC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs34589995 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107671968 | GGTTGTTATGCAATA[A/C]CAAAAAAGATAAATT | 10451 |
rs34597353 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957516 | TTTGGGATCCAGCAA[-/G]GGTAGGTAACACCAC | 10451 |
rs34600607 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925157 | TATTTACGTACACTT[-/A]AAAAAAAGAAATCAG | 10451 |
rs34619071 | snp | A/G | 0.277867 | 0.248442 | intron-variant | VAV3 | GRCh38.p7 | 1:107754334 | GGAAAACTGGCAGAT[A/G]ATGGTGTCCTGAAAT | 10451 |
rs34622809 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107943342 | TTGTAGATAAACTAC[-/A]AAAATTACATAAGAT | 10451 |
rs34631931 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590190 | GAAGAATTGCTACAC[C/T]ATTTGTCACCACACT | 10451 |
rs34638563 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107881959 | CTTAAAAGTGTATGG[G/T]TTCCTTTTTCTCTAT | 10451 |
rs34647076 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107932308 | GTGGTAGCTGAAGAG[-/T]ACTATAATTCAGTGA | 10451 |
rs34666353 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107712675 | ATAAAATGCTCATTT[-/A]AAAAAAAACTTATTA | 10451 |
rs34675242 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107765708 | TAACTCATATCACAT[-/G]GGAATCTGACCCACT | 10451 |
rs34681937 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107797362 | GAGTATCTGCATATG[-/C]CCATAAATTCTACTA | 10451 |
rs34688859 | multinucleotide-polymorphism | CT/TC | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107798347 | CACTGCTCAAGGTGG[CT/TC]CCTGCTCCCACACAC | 10451 |
rs34716039 | snp | C/G | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107800050 | TGGTTGAATAATATT[C/G]CATTGTGTACATATA | 10451 |
rs34725601 | in-del | -/TCTA | 0.282632 | 0.247861 | intron-variant | VAV3 | GRCh38.p7 | 1:107769313 | CACATATTTTGTGAC[-/TCTA]TCTAAGAAGTTAAGC | 10451 |
rs34725925 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940598 | ATCCATCAATGAATG[-/A]AAAAGCAAACAAAAA | 10451 |
rs34733924 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952757 | AACACAGGGTCAGGG[-/G]ATTGAGTTTCATTCA | 10451 |
rs34739480 | in-del | -/TG | 0.441432 | 0.160792 | intron-variant | VAV3 | GRCh38.p7 | 1:107778411 | TGCTTTAAAAAAATC[-/TG]TTTACATATAATAAC | 10451 |
rs34745618 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673767 | CTGGAAACATAGGCA[-/T]TTTAATAAACATGTG | 10451 |
rs34757997 | snp | G/T | 0.115088 | 0.210473 | intron-variant | VAV3 | GRCh38.p7 | 1:107800372 | TTATTCCCTGCCCTT[G/T]TTATAAAAGCCATTG | 10451 |
rs34760285 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107927406 | GATGCCTTCTGTTTG[-/A]AAAAAGAAGAGGAAA | 10451 |
rs34762897 | in-del | -/TATATGTTA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107925911 | ATGATATATATGTTA[-/TATATGTTA]CATATATAACATACG | 10451 |
rs34775096 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107775578 | GCAAGACTCAGTCAC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs34781032 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871743 | CAAAAGAAAACACAT[-/C]CCATATCAAGCCTAA | 10451 |
rs34802387 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107854701 | ATGTCATAATGACCT[-/A]CCCTGACCTTGAGAC | 10451 |
rs34803837 | snp | A/G | 0.34303 | 0.232046 | intron-variant | VAV3 | GRCh38.p7 | 1:107761318 | GAATGGAGTGAACCC[A/G]GGAGGCGGAGCTTGC | 10451 |
rs34816621 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107813968 | CTAAATAGTACTCCA[-/G]TGTGTGTGTGTGTGT | 10451 |
rs34822619 | snp | A/G | 0.0452528 | 0.143452 | intron-variant | VAV3 | GRCh38.p7 | 1:107692992 | TCATGTAGTGTAGTG[A/G]GGGGAAAAGCAAATG | 10451 |
rs34837829 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107779168 | AAAAAAAAAAAAAAA[-/A]GAAGAACCACACCAG | 10451 |
rs34849497 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107606804 | TCCAATGGTTTCTTC[-/T]TTTTTTTTTTTTTTT | 10451 |
rs34873492 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947502 | AACTGTCCACTACAT[-/G]CTCTGGTGCTGTGCT | 10451 |
rs34894399 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898204 | ATACATATATATAAT[-/G]GCATGTATACATGTA | 10451 |
rs34898030 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107837057 | AACTGACTCTACAAA[-/T]GCCAGCATCATCCTA | 10451 |
rs34900367 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107808504 | GAAATTTTATAGTAT[-/A]AAAAACTAACAAATG | 10451 |
rs34904602 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107881875 | TTGACGCTTAAAAAA[-/G]GGAAACATTTGAAGG | 10451 |
rs34918881 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107803329 | CTTGCTTTTCTAGTT[-/C]CCTTGAGGTGCATTA | 10451 |
rs34923712 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107664806 | AAGAGGGAATACTGG[-/A]AATTAAGTTTAGATG | 10451 |
rs34935666 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628647 | ACTATTTTTTCTACC[-/A]AAAAATAACAAAACT | 10451 |
rs34939574 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866069 | CTTGCAGGCAACCCA[-/C]CCTAAAGGAAGAATC | 10451 |
rs34959836 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107694560 | ACCTAATTTTCTACC[-/T]TTTCATTCATAAAGT | 10451 |
rs34964336 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107666310 | TCTTACTCTTAAGGG[-/A]AAAAAAATATAAGAG | 10451 |
rs34964914 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947009 | TCCAGAGGAAGCCAA[-/G]GGGAACCCAGAGGGA | 10451 |
rs34973130 | in-del | -/T | 0.434976 | 0.168179 | intron-variant | VAV3 | GRCh38.p7 | 1:107608066 | AAAAAAGAAAAGTAA[-/T]TTTAAAATTCTACTA | 10451 |
rs34989648 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107792098 | GAATGTAAGTACTTC[-/A]AATAGCTAACATTCC | 10451 |
rs35010844 | in-del | -/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588836 | CATCAAATTATTGAA[-/T]TTTCAGAATTCTTAG | 10451 |
rs35015224 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107942626 | TCTCCTAGCTTAGTC[-/T]TTTTCAGTCTACTAC | 10451 |
rs35015800 | in-del | -/G | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964169 | ACCAATGTCACTCCT[-/G]GGACAGATAACGGGA | 10451 |
rs35029715 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107660800 | ACTTAGAGTCTAACA[-/G]GGGAAAAGGAAAATT | 10451 |
rs35035008 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941399 | ATTGCTTTGGGCTGT[-/A]AAAAACTGCTTCCTG | 10451 |
rs35043244 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107631677 | TTCCCCTTCCTGTGT[-/C]CCATGTGTTCTCATT | 10451 |
rs35077144 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107696451 | CTCTGCCTACTCCCC[-/T]TTTTGGAATTGCCTT | 10451 |
rs35084025 | in-del | -/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796599 | CAATTTTCTGACACC[-/TG]GCTCCTTTAAAAATA | 10451 |
rs35100118 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107739072 | GTTTTAACCAGGGTA[-/C]ATGCTTATTTGCTGA | 10451 |
rs35119283 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732706 | GTAAACAAAGTGGCC[-/G]GGGAAGCTCGACCTG | 10451 |
rs35138453 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107891444 | CACGCACGATATACA[-/G]GGGGAAGAAAACTAG | 10451 |
rs35167306 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107803746 | GGTGACACATTCTGT[-/A]AAAGTCATTTAGGTC | 10451 |
rs35193329 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107872559 | TTAACACTATTCACA[-/T]TTTTTTCAACTTAAA | 10451 |
rs35195797 | in-del | -/A | 0.147656 | 0.228091 | intron-variant | VAV3 | GRCh38.p7 | 1:107957881 | AATTTTCTCCATCTT[-/A]AAAAAAAAAAAAAGA | 10451 |
rs35218373 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107706608 | CACAGGAACATATAA[-/G]GGATCTAGAAACAAA | 10451 |
rs35228691 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107706215 | GATGAGCCAGGATTT[-/C]CCCCTTTTATAGAAT | 10451 |
rs35229805 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107931147 | AGTGTAGAGGAAACA[-/T]TTTTGAGACAATCTA | 10451 |
rs35235016 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925643 | CAAATGCATAGGTAC[-/A]AAAAGTAGAATGGTG | 10451 |
rs35255880 | in-del | -/A | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591451 | ATGAATGAATGAATG[-/A]AATGAAGCAAATCCA | 10451 |
rs35259615 | snp | C/T | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107799747 | GTACATAGAGTCATG[C/T]TAACTACAGTCACTT | 10451 |
rs35275467 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107799934 | CCACATATGAGTGAG[-/A]AACATGTAATATTTG | 10451 |
rs35284717 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107799547 | CCACCAATAATTTTT[-/C]CCTTGAAAAATTTTT | 10451 |
rs35290300 | in-del | -/GT/GTGT | 0.322181 | 0.272602 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592056 | CATATATATACATAC[-/GT/GTGT]GTGTGTGTGTGTGTG | 10451 |
rs35297503 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673883 | ATTTGTCCAGAGAAC[-/T]TTTTTCTACACTTCC | 10451 |
rs35302381 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107694516 | TGAGCCTTTCCTTGC[-/A]AAAATACTAGAAAGG | 10451 |
rs35308556 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107836465 | CTAAATGCCTACATC[-/A]AAAAGTTTAAAAGTT | 10451 |
rs35313815 | snp | A/C/T | 0.00067766 | 0.0183955 | missense, upstream-variant-2KB, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107755464 | AACTGTTTAATTTCA[A/C/T]GAAGGGTCTCATTAT | 10451 |
rs35317053 | in-del | -/AC/ACACAC/ACACACACACAC | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107598801 | TGAGGTCTCTGGAAT[-/AC/ACACAC/ACACACACACAC]ACACACACACACACA | 10451 |
rs35321108 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107876948 | GTTTATCTTGGTTTG[-/T]TTTTTTTAATTTGCA | 10451 |
rs35323365 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954921 | ACTAAACCCCTCTTA[G/T]CTTCAGAGAGTATCC | 10451 |
rs35369057 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107770165 | CAGAGGGGCTCTCTC[-/G]GGGAATGATCTTCAT | 10451 |
rs35370700 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809513 | TTGCAAATATTTTAT[-/G]GAGCGTTTATAATGT | 10451 |
rs35380619 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | VAV3 | GRCh38.p7 | 1:107657400 | AAGAATCAGTTTTTA[C/T]TTTTTAAGAATTTCA | 10451 |
rs35391183 | in-del | -/A | 0.49975 | 0.0111793 | intron-variant | VAV3 | GRCh38.p7 | 1:107761393 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs35407613 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107648937 | GGAAGCAGGAAAGGA[-/G]GGAGGTAGAACTTTT | 10451 |
rs35433026 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107914451 | TTTATAGGTGAATTA[-/T]TTTGAGTCCTAATGC | 10451 |
rs35457852 | snp | C/T | 0.125874 | 0.217008 | intron-variant | VAV3 | GRCh38.p7 | 1:107757946 | CCAATTACTGTGAAA[C/T]GTATGTGCTCAACCC | 10451 |
rs35471974 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107798741 | AAAAAAAAAAAAAAA[A/C]AAAGAAGAACATGCA | 10451 |
rs35485771 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107749363 | GAAACAAAAACATCT[-/G]GGATTGATAAGCCAT | 10451 |
rs35487433 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107611852 | CTTCCCAGCCATGAT[-/G]CCATATTACTCAGGT | 10451 |
rs35495489 | in-del | -/C | 0.44306 | 0.158832 | intron-variant | VAV3 | GRCh38.p7 | 1:107616354 | GAAAAGCAAGTAACA[-/C]ATGTTCTCATTTATA | 10451 |
rs35498886 | in-del | -/CAT/TCA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107775220 | GTCTGCCTAAATAAC[-/CAT/TCA]AGTGAAAAGAACAAA | 10451 |
rs35521517 | in-del | -/G | | | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897680 | AGTGCATAAACCATA[-/G]GACTGCAGTTCCTCA | 10451 |
rs35530764 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107811181 | ACTTTCCACACTCAG[-/A]AAAAAAAGTCTTATC | 10451 |
rs35566473 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107810332 | GCAATGAGGACAGAA[-/G]GAGACATACACAGAA | 10451 |
rs35571026 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107653686 | TACATTTATCAGTTT[-/A]AAAATCAAGCAAATG | 10451 |
rs35587804 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107955000 | GATGAGATAATGCAT[-/G]GGAAAGCTTTAGTAA | 10451 |
rs35609784 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107851190 | GTGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs35619484 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107752091 | GACTTGTTTCCAAAA[C/T]TTATTGCAAAGCCAC | 10451 |
rs35621139 | in-del | -/T | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107800274 | GGAATCTCCAAACAG[-/T]TTTTCTATATTAGTT | 10451 |
rs35634996 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | VAV3 | GRCh38.p7 | 1:107850569 | CACATCAGGGCCTGT[C/T]GAGGGGTGGGGGGCA | 10451 |
rs35638520 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107881324 | TGTGTGGGGACGCAG[G/T]GGGAGAGAAAAGAGA | 10451 |
rs35652296 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673896 | ACTTTTTCTACACTT[-/C]CCTTATATTTTCCGA | 10451 |
rs35657301 | in-del | -/T | 0.499154 | 0.0205497 | intron-variant | VAV3 | GRCh38.p7 | 1:107701062 | TTGAGCTTTTTTTTT[-/T]CATATATGTGTTAGC | 10451 |
rs35660099 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925280 | TATGCTAACTACATA[-/G]GGAGAGTCAGTTTGT | 10451 |
rs35661702 | in-del | -/A | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590456 | ATTAAGCCTATATAC[-/A]AAATGCCTATAATTC | 10451 |
rs35664876 | in-del | -/A | 0.437118 | 0.165792 | intron-variant | VAV3 | GRCh38.p7 | 1:107639937 | GAAGACCCTGTATTT[-/A]AAAAAAAAAAAAAAA | 10451 |
rs35670917 | snp | C/T | 0.444444 | 0.157135 | intron-variant | VAV3 | GRCh38.p7 | 1:107875853 | AGACCAGAGTGTGGT[C/T]ACTTTTTGACTGTGT | 10451 |
rs35673194 | in-del | -/AAAT | 0.434109 | 0.169127 | intron-variant | VAV3 | GRCh38.p7 | 1:107720384 | GAGACACTGTCTCAA[-/AAAT]AAATAAATAAATAAA | 10451 |
rs35680239 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107845353 | AGGAAAAACCAGCAC[-/A]AAAAGGCTGAAAATA | 10451 |
rs35693360 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107891839 | GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs35700555 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107942049 | CTCCAAAAAACTTTG[-/A]AGAATGTTCCTTCAG | 10451 |
rs35707275 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107953944 | AAACTGAATACACTT[-/T]CTTGTAACACAGATT | 10451 |
rs35709018 | in-del | -/ATTT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107842222 | GACATTGCTTTAAAC[-/ATTT]AGTTCCCAAATTCTA | 10451 |
rs35711413 | in-del | -/TG | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107886955 | CATTACATTAACAAA[-/TG]TTCTACCAATTGTAT | 10451 |
rs35712191 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107584540 | TCCAGAATCTACAAT[-/G]GAACTCAAACAAATT | 10451 |
rs35721710 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107825486 | CCTAAGCCTATTCCT[-/C]CCTTAACAAATTTAA | 10451 |
rs35738519 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107687142 | GGTTAATTTATTTTA[-/G]GCTCTAAAGAAACTC | 10451 |
rs35750127 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621136 | CTTGGAGGTCCTTCA[-/G]GGAGGGAAAAAATTT | 10451 |
rs35754774 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107926991 | AGTGCTTGTACCACA[-/C]CCCCTCCCCTAACCC | 10451 |
rs35761581 | snp | C/T | 0.499897 | 0.00718776 | intron-variant | VAV3 | GRCh38.p7 | 1:107757907 | TCACAACCACTGTCA[C/T]AATGTCAACTATCAC | 10451 |
rs35767165 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107687345 | TCTTATATTTTGCTG[G/T]ACTTTTTCTTATTTT | 10451 |
rs35785244 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625644 | TTTTAACTCAGTGTG[-/A]AAGCGGTCTATTTTC | 10451 |
rs35785523 | in-del | -/A | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594491 | TTGTCAGAATCTCTT[-/A]AAAAGACTGGATAGG | 10451 |
rs35790538 | snp | A/C | 0.266546 | 0.249452 | intron-variant | VAV3 | GRCh38.p7 | 1:107747759 | ATTATGCAGCCAGTT[A/C]ATGGCAGTGATAATA | 10451 |
rs35811818 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107853904 | GTTTAACAGCCACTC[-/T]TTTCAGATCTGAACC | 10451 |
rs35814699 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107837103 | ATGGGCAAAAAAAAA[-/A]CAAAACGAAACAAAA | 10451 |
rs35817132 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794799 | TAATTTGAATTTCCC[-/T]TAGGGTCTGAGTATT | 10451 |
rs35826423 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582036 | TCTCACTCAGGTAAC[-/A]AAAAGTTGTTAGTAA | 10451 |
rs35827755 | snp | C/T | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107798545 | AACACAGTGTAAACC[C/T]CATCTCTACTAAAAA | 10451 |
rs35842075 | in-del | -/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591648 | ATCATCTCCACAACT[-/G]GAAAACTTCTATTCT | 10451 |
rs35845484 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107804755 | TTATACTTTCAAATA[-/T]TTTTGGTTTTTTTTG | 10451 |
rs35852784 | snp | C/T | 0.132066 | 0.220435 | intron-variant | VAV3 | GRCh38.p7 | 1:107772128 | TGACTTTTTCTGTTG[C/T]TGTTTCAAATTGTAA | 10451 |
rs35853527 | snp | C/G | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107800839 | TATATAATCCTATTT[C/G]TCTATCTTTGCTTTG | 10451 |
rs35862483 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941164 | TTGCAGTGGTGGCAA[-/C]CCGTAGTCCCTCCAG | 10451 |
rs35863270 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107605168 | CCAAATATACCTCCC[-/A]AAAATACATTTTTCA | 10451 |
rs35888872 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107935108 | CCAATGAGAACAATT[-/G]GGCAGTGTTCTACTT | 10451 |
rs35912633 | in-del | -/A | 0.21303 | 0.247251 | intron-variant | VAV3 | GRCh38.p7 | 1:107871505 | TGATTAAAAAAAAAA[-/A]GTGTAGAAAGCGTTT | 10451 |
rs35929287 | in-del | -/CC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814510 | CTTACTGTTGAGTTC[-/CC]AGTATATTCTGGATA | 10451 |
rs35932356 | snp | C/T | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107800820 | TGTAGAAACATTTTG[C/T]CTTTATATAATCCTA | 10451 |
rs35975364 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107948322 | TTGTAAAAAAAAAAA[-/A]TTGTAAGAGAATAAA | 10451 |
rs35988700 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107944492 | CTTATAACCTGAATT[-/A]CTTTGTTATATGTTC | 10451 |
rs36013101 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871036 | GCTCAGTAGGAAACA[-/T]TTTCCAAAGAGTGAG | 10451 |
rs36032866 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107801290 | ATTGCTTTAGCTATT[-/C]CAAGGTCATTTGGGG | 10451 |
rs36033211 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107674079 | ACACTGCAAAATAAT[-/C]CTGAAGGTAGTTTTT | 10451 |
rs36038876 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107642955 | AAGACACATATTTAT[-/C]CCCATGATCCCTGAC | 10451 |
rs36043434 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107863290 | TTTACAGTTGCTCTA[-/G]TAAAGGTCTGCATCA | 10451 |
rs36064785 | in-del | -/AAA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107945839 | AAAAAAAAAAAAAAG[-/AAA]GAAAGAAAAGAAAAA | 10451 |
rs36073688 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107834452 | TAACTACAGGAAATT[-/G]GGAATATTCAATTGA | 10451 |
rs36098349 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947019 | GCCAAGGGAACCCAG[-/A]AGGGAAAAGAGCCTG | 10451 |
rs36100691 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590223 | AAGGAACATGCTGAT[C/T]TACACTTTGTTTTCA | 10451 |
rs36116431 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107811036 | GGATAGTTCAACTTT[-/C]CAGAAGTCCTTTCTC | 10451 |
rs36119617 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107574229 | AGCAATGACAGTAGG[-/T]TTTGCAGTTCGTTAA | 10451 |
rs36120500 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625969 | AGAAAAAGGACCACA[A/T]CAGAATTTCTCAGAA | 10451 |
rs36155213 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945822 | GCAAAACTCCGACTC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs41278456 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107642946 | GTAATAGAATAAGAC[A/G]CATATTTATCCCATG | 10451 |
rs41278458 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107748912 | TTGGTTGTTCATTAT[A/T]CATAAGTGATTTAAC | 10451 |
rs41278460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751365 | AGCTCAGGTCTACAT[A/G]ACAAATAAGTCTGTC | 10451 |
rs41312682 | snp | A/C | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107768645 | ACCAAAATTGTAGAA[A/C]CTATTTTCTCTAACT | 10451 |
rs41481845 | snp | G/T | 0.0618563 | 0.164627 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963109 | TTCGAGGTTTAAAAA[G/T]GTCTTCAGCTGTCCA | 10451 |
rs41486546 | snp | A/T | 0.228547 | 0.249078 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756357 | AGACTTCCATTTAGA[A/T]CAAAGTTAGGAACTG | 10451 |
rs41517044 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107954092 | TAAAGCCAGTCACAA[A/G]TTGACATTCTGGTTT | 10451 |
rs55671314 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107667945 | GTGTCTGCTTGCCCT[C/T]TGCCCAACTGGGCCC | 10451 |
rs55676805 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | VAV3 | GRCh38.p7 | 1:107641699 | GGTAGGTAAAAAGCA[A/G]ATATGGTCAGAAATG | 10451 |
rs55682924 | in-del | -/A/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757185 | GTGTGTGTGTGTGTG[-/A/TA]TGTATGCAATTTGAA | 10451 |
rs55688733 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840935 | TTAAAAAAAAAAAAA[-/A]TTCATCTGGCAATCA | 10451 |
rs55703522 | snp | A/G | 0.000131876 | 0.00811915 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574170 | GTCATACCGAGCGAT[A/G]GCAATGCCCAGCACT | 10451 |
rs55707526 | snp | C/T | 0.116138 | 0.211142 | intron-variant | VAV3 | GRCh38.p7 | 1:107908746 | AGATGTGACAGCTGA[C/T]AGAAAAGGAGTAAGA | 10451 |
rs55710161 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107887128 | TTCAACCCTAAGGCT[C/T]TGGGCCAACCCAAGC | 10451 |
rs55711603 | snp | C/T | 0.225301 | 0.248777 | intron-variant | VAV3 | GRCh38.p7 | 1:107731595 | AAGGAAGAATCTTCT[C/T]CAGTTATTATAAGAA | 10451 |
rs55725323 | in-del | -/ATGTAT/ATGTATATGTATATGTAT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107728652 | TATATGTATATGTAT[-/ATGTAT/ATGTATATGTATATGTAT]TGTGTAAAACCGTGT | 10451 |
rs55730129 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107615933 | AAGAATGGCTTTTAT[-/T]AAAAAGTAAAAAAAT | 10451 |
rs55759434 | snp | C/T | 0.234982 | 0.249549 | intron-variant | VAV3 | GRCh38.p7 | 1:107717392 | TGCTATAAATTTCCC[C/T]CTATACACTGCTTTA | 10451 |
rs55774613 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107925158 | ATTTACGTACACTTA[A/T]AAAAAAGAAATCAGA | 10451 |
rs55792836 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923012 | TATCTCAGGTGTATA[C/T]ATCTATGAAACCACC | 10451 |
rs55798413 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107907630 | TGTCATAAAAGCAAA[G/T]CTGACCCCTCTTGCT | 10451 |
rs55800302 | snp | C/T | 0.0696718 | 0.173152 | intron-variant | VAV3 | GRCh38.p7 | 1:107641604 | ATGGGCAAACATCAA[C/T]ATGCTCACTTACTTT | 10451 |
rs55821232 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107783910 | AAAAAAAAAAAAAAA[-/A]TTAGCCAGGCATGGT | 10451 |
rs55824908 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107764959 | AATATTTTATAAAAT[G/T]GACATGAAATTATAT | 10451 |
rs55830758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107688231 | AACTTTTGCATTTTG[C/T]TCACAATCACTTGGT | 10451 |
rs55841742 | snp | A/C | 0.000389454 | 0.013949 | intron-variant | VAV3 | GRCh38.p7 | 1:107705102 | CTATAGAAAGTTTCA[A/C]AACAAAGCTGCAATT | 10451 |
rs55860424 | snp | A/G | 0.000504041 | 0.0158671 | intron-variant | VAV3 | GRCh38.p7 | 1:107574031 | ATGCACCAGCACATC[A/G]AGAGGGCCAACTTAC | 10451 |
rs55895734 | snp | A/G | 0.110167 | 0.207236 | intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964552 | CCAAAGCAGAAGGCT[A/G]GGAAGCAGGGCAAGC | 10451 |
rs55899408 | snp | C/T | 0.000394272 | 0.014035 | intron-variant | VAV3 | GRCh38.p7 | 1:107779510 | GAGAAAAGAGGAAAA[C/T]ACTAATTAGATATGT | 10451 |
rs55904472 | snp | G/T | 0.43978 | 0.162738 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595426 | TCTAGATATCCCAGT[G/T]TTGCTTAGGCTAAAG | 10451 |
rs55913072 | snp | A/G | 0.293294 | 0.246223 | intron-variant | VAV3 | GRCh38.p7 | 1:107746825 | CTCAGACTACAAGGT[A/G]ACCACTCTTAAGGAG | 10451 |
rs55964845 | in-del | -/CTCC/TCCC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107664339 | GATGCTCTCCCTCCC[-/CTCC/TCCC]CAACCCCCCACAAAA | 10451 |
rs56000657 | snp | A/C | 0.00203301 | 0.0318178 | intron-variant | VAV3 | GRCh38.p7 | 1:107617530 | ACAGGATCAAAAACA[A/C]AATGAAGCAAGAGAA | 10451 |
rs56004704 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107836430 | TAATGAGAGTAGTTT[-/T]AAGAGGAAAGTTTAT | 10451 |
rs56043852 | snp | C/T | 0.179425 | 0.239831 | intron-variant | VAV3 | GRCh38.p7 | 1:107617403 | ATATTAAAAAACATA[C/T]TCTGACAATAGAACT | 10451 |
rs56045116 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107849191 | CCTATTAAGCTACCA[C/T]TGACTTTCTTCACAG | 10451 |
rs56073558 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107948333 | TTGTAAAAAAAAAAA[A/T]TGTAAGAGAATAAAC | 10451 |
rs56077721 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107648189 | TGATGACTCAAATAA[A/T]GGAAATAGCACTGTC | 10451 |
rs56080321 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107642896 | TTTAAGTAACTATAA[C/T]AGAATGATTTTCAAC | 10451 |
rs56114126 | snp | C/T | 0.236144 | 0.249616 | intron-variant | VAV3 | GRCh38.p7 | 1:107720507 | AACATGGAGAAACCC[C/T]GTGTCTACTAAAAAT | 10451 |
rs56131616 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107596671 | AGTAATTATTGTTCT[C/T]ATTTATGAAATACTT | 10451 |
rs56161040 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | VAV3 | GRCh38.p7 | 1:107870322 | TGGTTTCTTAATTAT[A/G]GCCATTCTTGCAGGA | 10451 |
rs56188737 | snp | C/T | 0.389903 | 0.207189 | intron-variant | VAV3 | GRCh38.p7 | 1:107686259 | AGGTATGGTTATGGA[C/T]GCCCCACGGATTCTG | 10451 |
rs56193625 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964587 | CGCACCTAGACGTTT[A/G]CATTTACACAAAGAA | 10451 |
rs56197207 | snp | C/T | 0.0704125 | 0.17392 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590864 | GGACATCTGCAATAG[C/T]CTCCTAACTCATCTT | 10451 |
rs56202739 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107834331 | ATAAATTAGCCCCCT[C/T]CAGGATTAGCTCTCA | 10451 |
rs56218553 | snp | A/T | 0.148326 | 0.228391 | intron-variant | VAV3 | GRCh38.p7 | 1:107685253 | AATGGATTCTAGAAT[A/T]ATACTCCCTAAGTTC | 10451 |
rs56219073 | snp | C/T | 8.42694e-05 | 0.00649058 | intron-variant | VAV3 | GRCh38.p7 | 1:107704684 | AAGTGGTATATTAAA[C/T]GGTGCAAAATTCTGC | 10451 |
rs56262483 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107887129 | TCAACCCTAAGGCTC[G/T]GGGCCAACCCAAGCC | 10451 |
rs56266122 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107733689 | GAAGAGAAGTTTAGA[A/G]AAAAAAAAGTAAAAA | 10451 |
rs56268920 | snp | A/G | 0.013905 | 0.0822142 | intron-variant | VAV3 | GRCh38.p7 | 1:107766560 | AAGTTCCTAAGAAAA[A/G]AAAACAATGTGAAAG | 10451 |
rs56311947 | snp | A/G | 0.304937 | 0.243889 | intron-variant | VAV3 | GRCh38.p7 | 1:107817675 | GGGATCCATAGGCAG[A/G]GGGGTGAGGAGGCAA | 10451 |
rs56329228 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107791397 | ATCAAAAAAAAAAAA[-/A]GACTGCTGCAATAGT | 10451 |
rs56329640 | snp | A/G | 0.0611083 | 0.163768 | intron-variant | VAV3 | GRCh38.p7 | 1:107622298 | AACTACTTCAGGTTT[A/G]CTGGTAGAAATGATA | 10451 |
rs56340113 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107596147 | TTTGGAAGGAAGATG[-/T]TTAATGTTATTGTGC | 10451 |
rs56349449 | snp | A/G | 0.0422008 | 0.138995 | intron-variant | VAV3 | GRCh38.p7 | 1:107952161 | CATGTCTTTTGCAGA[A/G]ACATGGATAGCGCTG | 10451 |
rs56357780 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107757193 | TGTGTGTGTGTATGC[A/G]ATTTGAATTCCATTG | 10451 |
rs56357831 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892618 | CAAAAAATTAGTTAC[-/A]AAAAAAAAATGATGT | 10451 |
rs56357841 | snp | C/T | 0.225597 | 0.248806 | intron-variant | VAV3 | GRCh38.p7 | 1:107960778 | ACATTCCTGTGTTCC[C/T]TCACTCGCTTCAGGT | 10451 |
rs56375271 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107890956 | GGCAGATGTGGTGTA[G/T]GGTTTTATTATTTTG | 10451 |
rs56394543 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755693 | AGGCAATTTTAAAAT[A/G]TCTGAAGTACAGCTG | 10451 |
rs56410431 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571920 | GCTTCATTTCAGAGA[C/T]GATTCAAAATTTCAG | 10451 |
rs56675150 | snp | G/T | 0.0456336 | 0.143994 | intron-variant | VAV3 | GRCh38.p7 | 1:107659646 | ACAGAAATGTATCCC[G/T]ATTTAGTCATATTTT | 10451 |
rs56738244 | in-del | -/CCT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957311 | TCCCTCTATTCACCT[-/CCT]TTCTCTGGCCTTATC | 10451 |
rs56821281 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814993 | CCAGAAAATGTATGA[A/G]AGAGCCCCCAAAAGT | 10451 |
rs56935260 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107683970 | GACCAGACTGAAGAA[-/A]GGTATACAACCTCAA | 10451 |
rs56936311 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710366 | CAAATGTCAGTGCTT[C/T]AAAAACACCTGTCTG | 10451 |
rs56946912 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903628 | CACTACAGAAGCTGA[A/G]TATGCATCTTTATCC | 10451 |
rs56949608 | snp | C/G | 0.0569829 | 0.158885 | intron-variant | VAV3 | GRCh38.p7 | 1:107739891 | TTCTGGTTTTCCTTA[C/G]TATGCCCTCCAGGGA | 10451 |
rs56970538 | in-del | -/T | 0.112983 | 0.209108 | intron-variant | VAV3 | GRCh38.p7 | 1:107653781 | TGAAAATAGATAAAA[-/T]TTTTCCTTTAAATTC | 10451 |
rs56971422 | in-del | -/TT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107774928 | TTTTTTTTTTTTTTT[-/TT]AAGATAACCCTACTT | 10451 |
rs57081639 | in-del | -/TTTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107656966 | TTTTTTTTTTTTTTT[-/TTTT]CCGAGACGATGTCTC | 10451 |
rs57150009 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107838198 | AAGAAGAATATATTC[A/G]CAAACTATGCATCCG | 10451 |
rs57165709 | in-del | -/CTAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107717160 | TTGCTAGCAGTCTAT[-/CTAT]TTTGTTGATCTTTTC | 10451 |
rs57184485 | snp | A/T | 0.177824 | 0.239355 | intron-variant | VAV3 | GRCh38.p7 | 1:107579666 | TTCTTTCTCTTCTGT[A/T]CTAAATACTGCCTCA | 10451 |
rs57204590 | in-del | -/CG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107574998 | GTGTGTGTGTGCGTG[-/CG]TGCGCGCGCGCGCGC | 10451 |
rs57252447 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107779168 | ATGTTGGAGGAAAGT[A/T]AAAAAAAAAAAAAAA | 10451 |
rs57288177 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107798744 | AAAAAAAAAAAAAAA[-/A]GAAGAACATGCACCG | 10451 |
rs57314791 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107884431 | TATTATTATTATTAT[C/T]ATTATTATTATTATT | 10451 |
rs57336706 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | VAV3 | GRCh38.p7 | 1:107679431 | TATTTAAACATTTCC[C/T]ATCTACTCCACATAA | 10451 |
rs57355117 | snp | A/C | 0.207253 | 0.246318 | intron-variant | VAV3 | GRCh38.p7 | 1:107956474 | GATAAGCCTTTGAAA[A/C]GTACACAAGCATATA | 10451 |
rs57373404 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107620935 | ACCGTGGTTGTATAA[A/G]AAATGCTCTAAAACT | 10451 |
rs57379108 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575773 | TTCTAGTTTTAAATT[A/C]TATGATTTTTATTGG | 10451 |
rs57446262 | snp | A/G | 0.046775 | 0.145601 | intron-variant | VAV3 | GRCh38.p7 | 1:107847737 | ATAATTCAAATCCCT[A/G]CATAGACCAATAACA | 10451 |
rs57472214 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951822 | AGTCAAAAAAAAAAA[-/A]CATGCTGACAAGATT | 10451 |
rs57477480 | snp | G/T | 0.254385 | 0.249962 | intron-variant | VAV3 | GRCh38.p7 | 1:107916792 | AGTGAATGAATGAAT[G/T]AATACGATTCATGGA | 10451 |
rs57499233 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107676777 | TTTAGATATTTTGTT[C/T]CCTTGTCCTGTGTCC | 10451 |
rs57531367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107765701 | ACAGAAGATAACTCA[C/T]ATCACATGGAATCTG | 10451 |
rs57573343 | snp | G/T | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107868190 | CATAAAGCCCAAAGA[G/T]TTCTGGATAATTTGA | 10451 |
rs57605996 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | VAV3 | GRCh38.p7 | 1:107843014 | GAGAAAAAAGACAGA[C/G]AGAGAGAATGCTATT | 10451 |
rs57611993 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | VAV3 | GRCh38.p7 | 1:107578190 | CCCTCATATACACAC[G/T]GATGCATTAATGACA | 10451 |
rs57627547 | snp | G/T | 0.115438 | 0.210697 | intron-variant, nc-transcript-variant | VAV3, MIR7852 | GRCh38.p7 | 1:107897280 | TCATATGTAGGCATA[G/T]GTATGTAGTAGTCAA | 10451 |
rs57633962 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107606882 | TTGTTTGTTACTTAA[A/G]AAGGATGCATCCACA | 10451 |
rs57704822 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922965 | CAAAAAAAAAAAAGA[-/G]AAAAAAAAAAAAAGA | 10451 |
rs57795485 | in-del | -/GTTTT | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963756 | TTGGTTTTTTGTTTT[-/GTTTT]AACATTCTGAAAGAG | 10451 |
rs57910215 | snp | A/G | 0.225893 | 0.248835 | intron-variant | VAV3 | GRCh38.p7 | 1:107960415 | AGGTTGCAGTGAGCT[A/G]AGATCAGGCCACTGC | 10451 |
rs57961034 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107710166 | AGATGAAATCATCTG[C/T]AATGATCATGACCAA | 10451 |
rs58045478 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788130 | CTTGCCTCAATTATT[A/G]GAATAGCTTCCAATA | 10451 |
rs58066453 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107783236 | TTGAGAAAGTGTGGA[A/G]AGGACAATCACAGGG | 10451 |
rs58113303 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107710155 | AAATCCTAGCAAGAT[A/G]AAATCATCTGTAATG | 10451 |
rs58122070 | snp | A/G | 0.133093 | 0.220981 | intron-variant | VAV3 | GRCh38.p7 | 1:107959034 | CGGGAGGCCAAGGCG[A/G]CCTGATGACCTGAGG | 10451 |
rs58186016 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107580547 | CTGCCACCCAGTGTA[C/T]AGCTCTCAGCCAAAC | 10451 |
rs58195984 | in-del | -/TA | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107804861 | TGGTGGTGAATTCTC[-/TA]TAAACTTTTGTCTGT | 10451 |
rs58217386 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107803152 | ATAGTTTCTAATGAT[G/T]CTTTTTATTTCTGTG | 10451 |
rs58229730 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | VAV3 | GRCh38.p7 | 1:107649020 | GAAGGTAATAACTCC[C/T]AGTAATATATTCTAA | 10451 |
rs58239664 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107955318 | TCAGTGCTGGCTATG[-/T]TTTTTTTTTTAATTT | 10451 |
rs58281123 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822669 | AAAAAAATAAATAAA[-/T]AAATAAATAAATAAA | 10451 |
rs58301439 | snp | A/C | 0.030278 | 0.119257 | intron-variant | VAV3 | GRCh38.p7 | 1:107712812 | ATAATTCCACAAACA[A/C]TCATGAAACTGCAGC | 10451 |
rs58306950 | in-del | -/AT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107784078 | TATATATATATATAT[-/AT]TTCAAAAGAATACAT | 10451 |
rs58318688 | in-del | -/GTGTGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814010 | TGTGTGTGTGTGTGT[-/GTGTGT]ATACACACCATGTTT | 10451 |
rs58377830 | in-del | -/TA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107724893 | TGCCATTTGTGCATA[-/TA]CTCCAGAAATCTGAT | 10451 |
rs58379555 | in-del | -/GA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107915065 | TAGGCCCAACTAGGG[-/GA]ACTCACTTGAATAGT | 10451 |
rs58389950 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107630221 | ACATCATGGAGGCCT[C/G]CAGGTTAGAAACGGG | 10451 |
rs58535809 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710701 | ATCTTATTTTCCATA[C/G]CAAGGTTTTAAAATC | 10451 |
rs58588108 | snp | C/T | 0.179425 | 0.239831 | intron-variant | VAV3 | GRCh38.p7 | 1:107615530 | ATACCATTCTTGACA[C/T]AGGACCCAGCAAAGA | 10451 |
rs58611294 | snp | A/C | 0.447032 | 0.153878 | intron-variant | VAV3 | GRCh38.p7 | 1:107702809 | TCAAAAAAAAAAAAA[A/C]AACCTGATTTTTCAC | 10451 |
rs58611707 | in-del | -/AAATTAAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959271 | GTCTAAAAAATAAAT[-/AAATTAAT]TAATTAATTAATTAA | 10451 |
rs58620540 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107724790 | CATGTTCTGGAAGCT[G/T]CCAGGAAGGAATTCA | 10451 |
rs58621962 | in-del | -/GTGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757185 | TGTGTGTGTGTGTGT[-/GTGT]ATGCAATTTGAATTC | 10451 |
rs58665924 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107826216 | TACTATATTGTAAAT[A/C]CCTATCTACACGATT | 10451 |
rs58769688 | in-del | -/GGA/GGATGGAT/GGATGGATGGAT/GGATGGATGGATGGAT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107630380 | GATGGATGGATGGAT[lengthTooLong]AGGAGCCACTATTTA | 10451 |
rs58774169 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | VAV3 | GRCh38.p7 | 1:107867375 | ACTAAAGTTCTATAA[A/G]AGGAGGTAGGAATGG | 10451 |
rs58865681 | in-del | -/A | 0.414741 | 0.188044 | intron-variant | VAV3 | GRCh38.p7 | 1:107950130 | TGGAAACCACAAAAC[-/A]CAAAAAAAAAGTACT | 10451 |
rs58892985 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710367 | AAATGTCAGTGCTTC[A/C]AAAACACCTGTCTGA | 10451 |
rs58996761 | snp | A/G | 0.112631 | 0.208878 | intron-variant | VAV3 | GRCh38.p7 | 1:107643530 | ACTTATTCATTTACA[A/G]GTGAAACTGCTCCCA | 10451 |
rs59027575 | in-del | -/ACAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107849887 | AGAAAAAACAAACAA[-/ACAA]CCCCATCAAAAAGTG | 10451 |
rs59053660 | snp | A/G | 0.191775 | 0.243125 | intron-variant | VAV3 | GRCh38.p7 | 1:107922675 | GAGCACAATTTGGCC[A/G]GGCGCGGTGGCTCAC | 10451 |
rs59089703 | in-del | -/GCTAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107826279 | CATTTGCTCCATTAC[-/GCTAC]TTGCTATGCAGATTT | 10451 |
rs59093593 | snp | C/T | 0.218151 | 0.247963 | intron-variant | VAV3 | GRCh38.p7 | 1:107806835 | CCTCAGATAACAAAA[C/T]CTACAGATTCTCAAG | 10451 |
rs59211285 | in-del | -/CACA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107908872 | ACACACACACACACA[-/CACA]ATATAAAACATATTC | 10451 |
rs59226361 | snp | A/G | 0.39325 | 0.204889 | intron-variant | VAV3 | GRCh38.p7 | 1:107686465 | TTTCACTATTTACTT[A/G]TGAGAAGATTCCTGA | 10451 |
rs59290916 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | VAV3 | GRCh38.p7 | 1:107741055 | GGGGACAGGAAGGGA[A/G]GAGAGGACTAGCAGT | 10451 |
rs59364590 | snp | G/T | 0.469839 | 0.119042 | intron-variant | VAV3 | GRCh38.p7 | 1:107635625 | TAAAGTATAATAAAA[G/T]AAATTTTTTAAAAAA | 10451 |
rs59426924 | in-del | -/CAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107955279 | AGTAATGGCACTTAA[-/CAA]GTATTTTTGGTTTTT | 10451 |
rs59476510 | in-del | -/TGTGTGTGTG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624375 | TTATAGTCTTATGAC[-/TGTGTGTGTG]TGTGTGTGTGTGTGT | 10451 |
rs59567980 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757038 | GTAAAAAAAAAAAAA[-/A]TCCAGTTTTCTCCAC | 10451 |
rs59614404 | snp | G/T | 0.225893 | 0.248835 | intron-variant | VAV3 | GRCh38.p7 | 1:107959694 | ACTACTCCCTGTGTG[G/T]TATCACCCAGTCTCA | 10451 |
rs59717353 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922964 | CTCAAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAG | 10451 |
rs59769440 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107687613 | GGTTGAAGGTCAAGG[C/T]AATGATTGTCTGGGA | 10451 |
rs59790141 | in-del | -/GTTTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107906277 | GTTTTGTTTTGTTTT[-/GTTTT]TAAGAGAGAGGGTTT | 10451 |
rs59791582 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929309 | AAAAAAAAAAAAATT[-/T]ATGCCCTAGAACAGT | 10451 |
rs59806152 | snp | A/G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720381 | GAGTGAGACACTGTC[A/G/T]CAAAAATAAATAAAT | 10451 |
rs59815601 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | VAV3 | GRCh38.p7 | 1:107882622 | CCTATTTCTGTCCCT[C/T]TCACCATATCTTCTC | 10451 |
rs59832694 | snp | A/G | 0.232943 | 0.249417 | intron-variant | VAV3 | GRCh38.p7 | 1:107959127 | TTAGCCAGGCGTGGT[A/G]GCACACACCTGTAAT | 10451 |
rs59857751 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | VAV3 | GRCh38.p7 | 1:107917843 | AAATCCAGAATACTT[C/T]GATGAGCATTTCCTT | 10451 |
rs59908391 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107611337 | ATGGATTACATTTTT[-/T]AAAATCACAACTTTG | 10451 |
rs59969124 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107860353 | ATATGAGCGGTGATT[G/T]TAGTAGTTTTCTAGG | 10451 |
rs60049322 | snp | A/T | 0.21303 | 0.247251 | intron-variant | VAV3 | GRCh38.p7 | 1:107737409 | AAACTGCCATCAGAG[A/T]GAACAGGCAACCTAC | 10451 |
rs60051670 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107790085 | ATGCCATCCCAAAGC[C/G]CCCCCAGCTTGATAT | 10451 |
rs60072180 | in-del | -/GA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107835974 | TCCTTAGGGCTAGGG[-/GA]AAACACAGGCATGGT | 10451 |
rs60085246 | snp | A/C | 0.225893 | 0.248835 | intron-variant | VAV3 | GRCh38.p7 | 1:107959375 | TTACTCCCTAAAGAG[A/C]TGTCTATACTTGCTG | 10451 |
rs60098914 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107754419 | AAAGCAGCGATGAAA[C/T]TGCTCTACCAAAAAT | 10451 |
rs60163431 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107693372 | AACAAAATAAACTTA[A/C]CACATCTTTTTTTCA | 10451 |
rs60171013 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918709 | TATATATATATATTT[A/T]TTTTTTTTTTTGAGA | 10451 |
rs60182456 | snp | C/T | 0.464416 | 0.128553 | intron-variant | VAV3 | GRCh38.p7 | 1:107640338 | GGAATCTCAAGATAA[C/T]CATGTTGTGTGAAAT | 10451 |
rs60207273 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724846 | GGGGGAAAAAAAAAA[-/AA]GGCTAGAGCTGAGCA | 10451 |
rs60237207 | snp | G/T | 0.436265 | 0.166749 | intron-variant | VAV3 | GRCh38.p7 | 1:107580810 | TTGATAAAAATATTT[G/T]TAGAATGATTTAACC | 10451 |
rs60249796 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107645322 | ATATAATGGAATGTA[-/T]TTTTTTTTTTTTTGG | 10451 |
rs60261760 | snp | A/T | 0.440333 | 0.16209 | intron-variant | VAV3 | GRCh38.p7 | 1:107599943 | ATAAAAGGTAACTCC[A/T]TGAAGTCTGTATGAT | 10451 |
rs60284097 | in-del | -/AAACA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107598377 | AAACAAAACAAAACA[-/AAACA]CCAAAAAACACACAC | 10451 |
rs60440691 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107860354 | TATGAGCGGTGATTG[C/T]AGTAGTTTTCTAGGT | 10451 |
rs60442733 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107638558 | GAGGAGTATAGTATG[C/T]TCAGTGATTAGAAGA | 10451 |
rs60473359 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107710416 | TATCAAAAATACATC[A/G]ATTTATAAAAATGTA | 10451 |
rs60495917 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107821623 | ACGTCCACAGTAAAA[-/A]TGGAAGACAGAGGAG | 10451 |
rs60517967 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107865125 | AGGCTGAGCAACTTT[C/T]CTGCACACAGGTGGC | 10451 |
rs60555746 | in-del | -/A | 0.46974 | 0.119223 | intron-variant | VAV3 | GRCh38.p7 | 1:107624445 | TACCTTTAATGATAG[-/A]AAAAAAAAATTTGGC | 10451 |
rs60557678 | in-del | -/AC/ACACACACAC | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107598823 | CACACACACACACAC[-/AC/ACACACACAC]GTATACATAATGTCA | 10451 |
rs60559311 | snp | C/G | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107951965 | CCCAGCAATCCCATT[C/G]CAGGATATACACCCA | 10451 |
rs60592136 | in-del | -/A/AAA/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929308 | AAAAAAAAAAAAAAA[-/A/AAA/T]TTATGCCCTAGAACA | 10451 |
rs60625329 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | VAV3 | GRCh38.p7 | 1:107825642 | TGCAAATGCTTTGAC[C/T]TTTCCTACCCCAATG | 10451 |
rs60645690 | snp | C/T | 0.463451 | 0.130149 | intron-variant | VAV3 | GRCh38.p7 | 1:107635270 | TGTAGCAGATATACA[C/T]CAAGGAATACTATGC | 10451 |
rs60656336 | snp | A/G | 0.104504 | 0.2033 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897388 | ATTGAAAAAGTAGAG[A/G]GAGAAAGAGAGAAAA | 10451 |
rs60699898 | in-del | -/AT/ATAT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107757190 | TGTGTGTGTGTGTAT[-/AT/ATAT]GCAATTTGAATTCCA | 10451 |
rs60709561 | in-del | -/GTGA/GTGTGA/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624413 | TGTGTGTGTGTGTGT[-/GTGA/GTGTGA/TG]GAAAGAAACAAGAGA | 10451 |
rs60806616 | in-del | -/TA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107612197 | CTATATATATATATA[-/TA]AATAAATATATATGT | 10451 |
rs60811690 | snp | A/G | 0.110167 | 0.207236 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963773 | TTTAACATTCTGAAA[A/G]AGAAAGAGGCTCTGA | 10451 |
rs60860131 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107710338 | TTGAAAGTAAAAGTA[A/G]GAGAGCTGGAAGCAA | 10451 |
rs60870977 | in-del | -/T/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107601790 | ATTTTTTTTAAACTG[-/T/TG]GGAATAATCCTTATT | 10451 |
rs60880122 | in-del | -/ACACGCGCGCGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575017 | CGCGCGCGCGCGCGC[-/ACACGCGCGCGT]GTTTAATATTCGATG | 10451 |
rs61021918 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963927 | ACCCTCAAAGAGGCA[A/G]CTCCAGCCCCAGGAG | 10451 |
rs61056304 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | VAV3 | GRCh38.p7 | 1:107904219 | CTTCCTTCCTCAATT[A/G]AGTTAAAATGCTGAT | 10451 |
rs61127542 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107607316 | AAGGTCTGGATTTTA[A/G]ATTTTTAACTCTATT | 10451 |
rs61137252 | snp | A/C | 0.170084 | 0.236883 | intron-variant | VAV3 | GRCh38.p7 | 1:107951497 | TTAACTAAAGAGCTT[A/C]TGCACAGCAAAAGAA | 10451 |
rs61138298 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107610625 | GAAAATACTTATTTT[C/T]CCATTTGTTTCACAT | 10451 |
rs61158212 | snp | C/T | | | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690257 | AACCTATGATAACCC[C/T]ATGTGTCAGTAGTTG | 10451 |
rs61192238 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107717455 | TTTGTTCTCATTGGT[G/T]TCAAAGAACATCTTT | 10451 |
rs61214050 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903791 | ATTTATATTTTCTGA[A/G]AACTGACACCTCCAT | 10451 |
rs61253571 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107710046 | TATGATTTTTAAAAC[A/T]TACATGCTTAAAATG | 10451 |
rs61276973 | in-del | -/TT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107586156 | TTTTTTTTTTTTTTT[-/TT]CCCAGAGCGCTCAGT | 10451 |
rs61283572 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107698361 | GCTACCAGTCAGCCA[C/T]GAAATCACAAGGGGA | 10451 |
rs61293909 | snp | A/T | 0.0648419 | 0.167978 | intron-variant | VAV3 | GRCh38.p7 | 1:107904220 | TTCCTTCCTCAATTG[A/T]GTTAAAATGCTGATT | 10451 |
rs61357995 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | VAV3 | GRCh38.p7 | 1:107739350 | TGACAGCTGTGATTT[C/T]TCTGAGCACTGTCCC | 10451 |
rs61393664 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107868177 | GTCCCATGGATGACA[A/T]AAAGCCCAAAGATTT | 10451 |
rs61419143 | in-del | -/A | 0.0648419 | 0.167978 | intron-variant | VAV3 | GRCh38.p7 | 1:107903663 | TGCAGGATTTTCACT[-/A]AAAACTAACAAAACT | 10451 |
rs61471569 | snp | C/G | 0.239614 | 0.249784 | intron-variant | VAV3 | GRCh38.p7 | 1:107716445 | GTTTTTAGCATGAAG[C/G]GCTGTTCAATTTTGT | 10451 |
rs61530288 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107801364 | ATCACTGATATTTTG[A/G]TAAGGACTGCATTGA | 10451 |
rs61544976 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107607142 | TGTATTTTTAGTAGA[A/G]ATGGGGTTTCACTAT | 10451 |
rs61550499 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107826217 | ACTATATTGTAAATC[C/T]CTATCTACACGATTA | 10451 |
rs61599464 | snp | C/T | 0.463881 | 0.12944 | intron-variant | VAV3 | GRCh38.p7 | 1:107622147 | AACTAAAATTATTGA[C/T]AACTTCTTCTGACAT | 10451 |
rs61651323 | snp | C/T | 0.117886 | 0.21224 | intron-variant | VAV3 | GRCh38.p7 | 1:107923520 | TAAGACTGGTTAATT[C/T]ATAAAGAAAAGAAGT | 10451 |
rs61671261 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107710288 | TTGTGGCAATTATGT[A/G]GTATACATAAAATGG | 10451 |
rs61761613 | snp | A/C/G | 0.000298542 | 0.0122143 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874915 | CCTTTCCAAAGTCAC[A/C/G]AACATCAAACAAGTC | 10451 |
rs61761614 | snp | C/T | | | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107770712 | CAACAACTTCGTATA[C/T]CATTTTCTGGACATT | 10451 |
rs61797268 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954532 | TCAGTATCCTGAGGC[A/T]AATTTTTTTTTTTTT | 10451 |
rs61797269 | snp | A/C | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966061 | TTTGGAGACTCTAAA[A/C]CCTACCCCTTTTACT | 10451 |
rs61797407 | snp | C/T | 0.130351 | 0.219509 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788439 | CTCCAGGCCAACACA[C/T]AGAAATTCCAGCAGA | 10451 |
rs61797408 | snp | C/T | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107798347 | CACTGCTCAAGGTGG[C/T]TCCTGCTCCCACACA | 10451 |
rs61797410 | snp | C/T | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107798667 | GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTG | 10451 |
rs61797416 | snp | C/T | 0.114738 | 0.210248 | intron-variant | VAV3 | GRCh38.p7 | 1:107802436 | ATCTTAGCAAAAAGG[C/T]CTTCAATTTTTCCCC | 10451 |
rs61797987 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107813104 | AGCCTAAGCGACAGA[A/G]CCAGACTCCGTCTCA | 10451 |
rs61797988 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107859185 | TTGACCTCCTCCCAC[C/T]TCAGCCTCCTGAATA | 10451 |
rs61798726 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107907657 | TGCTCTCGTGTGCGT[G/T]CGTTCTCTCTCTCTC | 10451 |
rs61798727 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923174 | GTTAAATTGCCTTTT[A/C]TAAAACTGTATATAA | 10451 |
rs61798728 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107944826 | GCCCAGGCTGGTCTC[G/T]AACTCCTGAGCTCTG | 10451 |
rs61798872 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107630317 | TATGAATGGATGAAT[G/T]GTAGGATAAAAAGAT | 10451 |
rs61798873 | snp | A/G | 0.470618 | 0.117591 | intron-variant | VAV3 | GRCh38.p7 | 1:107630345 | GATGGAAGAATGGAT[A/G]GGAGGATGGATGGAT | 10451 |
rs61798874 | snp | C/T | 0.46974 | 0.119223 | intron-variant | VAV3 | GRCh38.p7 | 1:107631459 | TTCCACTCTAGTATA[C/T]TTTCTCTTTTTTAAT | 10451 |
rs61798875 | snp | A/G | 0.463666 | 0.129795 | intron-variant | VAV3 | GRCh38.p7 | 1:107634809 | CATGAAAAAGTGGGC[A/G]AAGGATATGAACAGA | 10451 |
rs61798887 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107665793 | CTCCATGTCAGTATT[A/G]CTGCATACCTACTAG | 10451 |
rs61798888 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | VAV3 | GRCh38.p7 | 1:107671588 | TAATAGGTCTAGTCT[C/T]ACTCCCAGGAGCAGC | 10451 |
rs61798889 | snp | C/T | 0.378962 | 0.21417 | intron-variant | VAV3 | GRCh38.p7 | 1:107676971 | GCAGAGGAACTTCCA[C/T]GTTTCTAATACCTAT | 10451 |
rs61798890 | snp | C/T | 0.386504 | 0.209444 | intron-variant | VAV3 | GRCh38.p7 | 1:107685459 | AGATTATTAGCTTTT[C/T]GTTATTTTAAATGTT | 10451 |
rs61798893 | snp | A/T | 0.314544 | 0.241524 | intron-variant | VAV3 | GRCh38.p7 | 1:107698204 | GATGGTTCATTTATG[A/T]TTTTTCCACTTTACA | 10451 |
rs61798894 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107708211 | AAGAAAAAAAAAAGT[A/T]CTGCTGCTACTACAT | 10451 |
rs61798911 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733538 | AAACAGTGTAGAGAA[A/G]ACCTTAAATGACCTG | 10451 |
rs61798913 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107741385 | CTGTCCGGCCTGACT[A/G]GCCGCTCCCTGAAGG | 10451 |
rs61798914 | snp | C/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107745819 | CACTCTTAAAAATAT[C/G]AGCTCCCTTGATTTC | 10451 |
rs61799821 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | VAV3 | GRCh38.p7 | 1:107753706 | CTGGGACTACAGGCA[C/T]GTGCCACCATGCCTG | 10451 |
rs61801407 | snp | A/C | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570816 | ATTTCTCAGGACCGA[A/C]TGACCCATGTCCAAC | 10451 |
rs61801408 | snp | C/T | 0.031488 | 0.12146 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570827 | CCGAATGACCCATGT[C/T]CAACTGCTGTTCACA | 10451 |
rs61801409 | snp | C/T | 0.268995 | 0.249277 | intron-variant | VAV3 | GRCh38.p7 | 1:107574998 | GTGTGTGTGTGCGTG[C/T]GTGCGCGCGCGCGCG | 10451 |
rs61801411 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107586160 | TTTTTTTTTTTTTCC[C/T]AGAGCGCTCAGTAAC | 10451 |
rs61801412 | snp | A/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592079 | TGTGTGTGTGTGTGT[A/G]TGTATCTTCCCAACC | 10451 |
rs62618754 | snp | C/T | 0.00953873 | 0.0683987 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573249 | GCTTTTTAAACACTT[C/T]AGTTAATTCACGATG | 10451 |
rs62724663 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107720469 | AAAAAAAAAAAAAAA[A/G]GGAGTTTGAGACCAG | 10451 |
rs66477614 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107606965 | GTCTGATCTTTTTTT[-/T]TTTTTTTAAGATGAA | 10451 |
rs66480516 | multinucleotide-polymorphism | CA/TG | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107746033 | TTTTCTTTTATTCTC[CA/TG]TGACTTATCAAAAAG | 10451 |
rs66493650 | in-del | -/C | 0.497613 | 0.0344622 | intron-variant | VAV3 | GRCh38.p7 | 1:107794352 | TTGATTCATCATTTT[-/C]TCCCTTCATCTTGCT | 10451 |
rs66609632 | in-del | -/AC/C/CA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107778412 | TGTTATTATATGTAA[-/AC/C/CA]AGATTTTTTTAAAGC | 10451 |
rs66634099 | in-del | -/G | 0.497933 | 0.032082 | intron-variant | VAV3 | GRCh38.p7 | 1:107945838 | AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAAGAA | 10451 |
rs66634100 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107945838 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAAGAA | 10451 |
rs66707621 | in-del | -/AAA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107918718 | AAAACTCCATCTCTC[-/AAA]AAAAAAAAAATATAT | 10451 |
rs66747247 | in-del | -/TAG | 0.295854 | 0.245759 | intron-variant | VAV3 | GRCh38.p7 | 1:107675410 | GACTATATAGCTAGT[-/TAG]TAGAGAGGCAGGACA | 10451 |
rs66866060 | in-del | -/AAAAA | 0.375 | 0.216506 | intron-variant | VAV3 | GRCh38.p7 | 1:107866844 | AAAAAAAAAAAAAAA[-/AAAAA]TAGGGCATTTGTAAC | 10451 |
rs66867103 | in-del | -/T | 0.289683 | 0.24683 | intron-variant | VAV3 | GRCh38.p7 | 1:107692031 | TGTGTTTAGTCTGAA[-/T]AGAACTTCAGATAAG | 10451 |
rs66909735 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681655 | AAAAAAAAAAAAAAA[-/A]GTTTTCCATTACGTA | 10451 |
rs66956697 | in-del | -/TTG | 0.611111 | 0.124226 | intron-variant | VAV3 | GRCh38.p7 | 1:107874731 | GTGGGGTTTCTTTTT[-/TTG]TGTTGTTGTTTTTTG | 10451 |
rs66982121 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107611608 | TTTGTTTTTTTTTTT[-/T]GGTTCTCTATGGAAA | 10451 |
rs67028280 | snp | C/T | 0.316243 | 0.241064 | intron-variant | VAV3 | GRCh38.p7 | 1:107666517 | AGCACAGAAGATCAC[C/T]GTGGCTTCTGATCCC | 10451 |
rs67152997 | in-del | -/AC | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107886956 | AATACAATTGGTAGA[-/AC]ATTTGTTAATGTAAT | 10451 |
rs67263579 | in-del | -/A | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107656969 | GAGACATCGTCTCGG[-/A]AAAAAAAAAAAAAAA | 10451 |
rs67439905 | in-del | -/TATACTCGAGTATACAGAGTATACACTAGTATACTCTG | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107644983 | CACTAGTATACTCTG[lengthTooLong]GTCAAGTAATAGGAC | 10451 |
rs67634108 | in-del | -/A | 0.311123 | 0.242413 | intron-variant | VAV3 | GRCh38.p7 | 1:107700276 | ATAAAACTTTAAAAA[-/A]TGCTTATTGCTCATG | 10451 |
rs67666662 | in-del | -/T | 0.336245 | 0.234652 | intron-variant | VAV3 | GRCh38.p7 | 1:107922965 | TCTTTTTTTTTTTTT[-/T]CTTTTTTTTTTTTGA | 10451 |
rs67668167 | in-del | -/AAAA | 0.465263 | 0.127129 | intron-variant | VAV3 | GRCh38.p7 | 1:107702796 | AAGCCCACGTCTTTC[-/AAAA]AAAAAAAAAAAACCT | 10451 |
rs67778148 | snp | G/T | 0.304937 | 0.243889 | intron-variant | VAV3 | GRCh38.p7 | 1:107815880 | CCAGACCCGTGGCGG[G/T]GTGTGGAGGGGGCAT | 10451 |
rs68033870 | in-del | -/ATACAC | 0.460252 | 0.135255 | intron-variant | VAV3 | GRCh38.p7 | 1:107893052 | GAAAGAATTAAAAAT[-/ATACAC]AGAGTAAAAAACTTG | 10451 |
rs71098639 | in-del | -/CACACA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107624409 | TTCTCTTGTTTCTTT[-/CACACA]CACACACACACACAC | 10451 |
rs71098641 | in-del | -/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107635488 | CCTAATGCTATCCCT[-/C]CCCCCCTCCCCCCAC | 10451 |
rs71098642 | in-del | -/TCCC | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107651567 | TTGGGAGAGAAAGGG[-/TCCC]TCCCTCCCTCCCTCC | 10451 |
rs71098643 | in-del | -/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107686042 | GTTCCTGCCCCCCCT[-/C]CCCCCCCCACCCCCC | 10451 |
rs71098644 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107720468 | TGGTCTCAAACTCCT[-/T]TTTTTTTTTTTTTTA | 10451 |
rs71098647 | in-del | -/T | 0.329317 | 0.237084 | intron-variant | VAV3 | GRCh38.p7 | 1:107766914 | TAGTGAGATAATTTC[-/T]TTTTTTCACAGGATG | 10451 |
rs71098652 | in-del | -/AG/GA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107885259 | AAAAATAAAAATAAA[-/AG/GA]AAATAAAAGCGACAG | 10451 |
rs71098654 | in-del | -/G | 0.492237 | 0.0618148 | intron-variant | VAV3 | GRCh38.p7 | 1:107926578 | ACCAGGAGATGGGGG[-/G]AGGGGTGGCATCCAT | 10451 |
rs71275977 | in-del | -/A/AAAA | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107621102 | TCCTTTAAAAGAGGT[-/A/AAAA]AAAAAAAAAAAAATG | 10451 |
rs71589172 | in-del | -/GTGT | 0.5 | 0 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592078 | TGTGTGTGTGTGTGT[-/GTGT]ATGTATCTTCCCAAC | 10451 |
rs71589174 | in-del | -/A | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107672291 | AAAAAAAAAAAAAAA[-/A]GATAAATTTAAATTC | 10451 |
rs71589175 | in-del | -/ATTGT | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107728655 | ATGTATATGTATTGT[-/ATTGT]GTAAAACCGTGTCCC | 10451 |
rs71589178 | in-del | -/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107758898 | TCCCATTAGAAATAT[-/T]ATTTTTTCTGCTTAC | 10451 |
rs71589180 | in-del | -/TTGT | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107798393 | CAGGCAGGTGGCTGT[-/TTGT]GCCTCCAATAAGCAG | 10451 |
rs71589181 | in-del | -/GTTGA | 0.498437 | 0.0279115 | intron-variant | VAV3 | GRCh38.p7 | 1:107814500 | ATGAGATTACTTACT[-/GTTGA]GTTGAGTTCCCAGTA | 10451 |
rs71589185 | in-del | -/CC | 0.5 | 0 | intron-variant, nc-transcript-variant | VAV3, MIR7852 | GRCh38.p7 | 1:107897230 | AAATTAATAAATGCC[-/CC]TTTGACTACTACATA | 10451 |
rs71644379 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107582566 | CTGTTGTGGGGTGGG[A/G]GGAGGGGGGAGGGAT | 10451 |
rs71655920 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107582865 | GTGAATAGTGATGCA[A/G]TAAACATACGTGTGC | 10451 |
rs71655921 | snp | A/C/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107582874 | GATGCAATAAACATA[A/C/G]GTGTGCATGTGTCTT | 10451 |
rs71655922 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107606975 | TTTTTTTTTTTTTAA[A/G]ATGAAATCTCACACT | 10451 |
rs71655923 | snp | C/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107607112 | GGCACCCACAACCAC[C/G]CCCAGCTAATTTTTT | 10451 |
rs71655925 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107612078 | AACTTCTGCTATGAA[C/T]ATGTAGTTTTTAAAA | 10451 |
rs71655926 | snp | A/G | 0.26518 | 0.249539 | intron-variant | VAV3 | GRCh38.p7 | 1:107634352 | TCTTTGACAAACCTG[A/G]CAAAAAGAAGAAATA | 10451 |
rs71655927 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107652226 | CCTCTCCTAGTCCTC[A/G]CTGCTACACTCCCAC | 10451 |
rs71655928 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107660745 | CTGCTTGGAATGTGA[A/C]CAACATAATAAACAA | 10451 |
rs71655929 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107676431 | CAGACAACTTTGCCT[C/T]CACATGAGAAAAACC | 10451 |
rs71655930 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | VAV3 | GRCh38.p7 | 1:107695039 | ACATTAAGTTTACTA[A/G]ACAGAAAAGGGAAGG | 10451 |
rs71655931 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107733335 | AGGGCCTCTTCTCCT[C/T]CAAAGGATCGCAGCT | 10451 |
rs71655932 | snp | A/C | 0.178465 | 0.239547 | intron-variant | VAV3 | GRCh38.p7 | 1:107734277 | AATTGTAAAGACCAG[A/C]AATGCTAGGAAGACA | 10451 |
rs71655933 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107844639 | GCTTGGTGGGGGAGG[A/G]AGGCTTGAGTAGGCA | 10451 |
rs71655934 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107859003 | TTCTCTTTTTTGTTG[G/T]TGTTTAGCCAGATAA | 10451 |
rs71655935 | snp | C/G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107859006 | TCTTTTTTGTTGTTG[C/G/T]TTAGCCAGATAAAAA | 10451 |
rs71655936 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107880273 | AGTGGTTGGTGTTTA[A/G]AAGGCAGAAAGGCAA | 10451 |
rs71655937 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107891672 | GGTGAAACCCCGTCT[C/T]TACTAAAAATACAAA | 10451 |
rs71655938 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107909794 | ATAGATGTTCTTTAA[A/T]TGTGTTATCTTCTTT | 10451 |
rs71655939 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107942548 | CTCTTTTCCTTTTTA[A/T]ATCTGTGTATCCTGA | 10451 |
rs71655940 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963223 | GTGGGCCAAGGCATC[C/T]TGACCCACGCTGCCT | 10451 |
rs71684098 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898104 | TGTCATTATTAAATT[-/A]AAAAAAAAAAGGAAG | 10451 |
rs71688216 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866823 | CGAGACTCCATCTCA[-/AA]AAAAAAAAAAAAAAA | 10451 |
rs71701572 | in-del | -/AAATT | 0.326035 | 0.238157 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896382 | CTGTCCTCTTTCATC[-/AAATT]AATCGCACAGCAGCC | 10451 |
rs71741074 | in-del | -/T/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796799 | ATTTGTAAAAAAAAA[-/T/TA]AAAAAATATATATAT | 10451 |
rs71787716 | in-del | -/AT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107612194 | GGTCTATATATATAT[-/AT]ATAAATAAATATATA | 10451 |
rs71796067 | in-del | -/GCC | 0.45843 | 0.138046 | cds-indel, intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964920 | GGCGGCAAGGATGCG[-/GCC]GCCGCCGCCGCCGCC | 10451 |
rs71924623 | in-del | -/AG | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107910133 | GAAATGAACTTGAAG[-/AG]GTTATTCTGAATGCC | 10451 |
rs71971498 | in-del | -/GC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107574993 | TGTGTGTGTGTGTGT[-/GC]GTGCGTGCGCGCGCG | 10451 |
rs72025041 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794354 | GATTCATCATTTTCT[-/C]CCTTCATCTTGCTTT | 10451 |
rs72093932 | in-del | -/GTTGA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814501 | TGAGATTACTTACTG[-/GTTGA]TTGAGTTCCCAGTAT | 10451 |
rs72129870 | in-del | -/TT | 0.263506 | 0.249635 | intron-variant | VAV3 | GRCh38.p7 | 1:107645322 | ATATAATGGAATGTA[-/TT]TTTTTTTTTTTTGGT | 10451 |
rs72283906 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764324 | CCTAACTCAAATGCG[-/T]CCTCTTCAGATGAAT | 10451 |
rs72392700 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933289 | TTTTTTTGTGTTTTT[-/T]TTTTTTCCAGTACAA | 10451 |
rs72502356 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764322 | GACCTAACTCAAATG[-/T]CGCCTCTTCAGATGA | 10451 |
rs72689607 | snp | A/C | 0.0524604 | 0.153226 | intron-variant | VAV3 | GRCh38.p7 | 1:107872225 | TCTTAGCTTCCTCAT[A/C]TGAAGAATGTCTTCA | 10451 |
rs72689608 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107873024 | ATACAGTTCTAAAGA[A/G]ATAGCTACTCCAATC | 10451 |
rs72689610 | snp | A/C | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107873025 | TACAGTTCTAAAGAG[A/C]TAGCTACTCCAATCT | 10451 |
rs72689614 | snp | A/G | 0.173965 | 0.238157 | intron-variant | VAV3 | GRCh38.p7 | 1:107876198 | TCAGATGCTGCAGAC[A/G]GCCAAATAGGATTTA | 10451 |
rs72689617 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | VAV3 | GRCh38.p7 | 1:107882036 | GATGGCTTCCCTTTT[C/T]ATTTGAAAAAATAAA | 10451 |
rs72689620 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | VAV3 | GRCh38.p7 | 1:107882231 | ATGTAGATTTTCTAA[C/G]TTATATTTGATGAGG | 10451 |
rs72689621 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | VAV3 | GRCh38.p7 | 1:107882684 | ATCTTACATCTCCTA[A/G]AAATTTAATAAAAGA | 10451 |
rs72689623 | snp | G/T | 0.0349115 | 0.127424 | intron-variant | VAV3 | GRCh38.p7 | 1:107886216 | ATATGTCCCAGGTAT[G/T]ACACTAAGAACTTGC | 10451 |
rs72689625 | snp | A/G | 0.173643 | 0.238054 | intron-variant | VAV3 | GRCh38.p7 | 1:107888754 | ATGAGCCACTGGGCC[A/G]GGCCTACCCTGACTC | 10451 |
rs72689640 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107954742 | CTCCTCCAAGGGAGC[C/T]CCACACAACAGGAAA | 10451 |
rs72689643 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | VAV3 | GRCh38.p7 | 1:107957302 | TCCTCTCTATCCCTC[C/T]ATTCACCTCCTTTCT | 10451 |
rs72703503 | snp | A/C | 0 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570976 | AGCGGCCCTCCTACT[A/C]GACGCATAGCGTCCA | 10451 |
rs72703505 | snp | C/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107574967 | GTTGAGTTTCTCTGT[C/G]TGTGTGTGTGTGTGT | 10451 |
rs72703511 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107603423 | TAAATGGGACACAGA[A/G]GAGTCAGTGGGTATT | 10451 |
rs72703574 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | VAV3 | GRCh38.p7 | 1:107617253 | AGACCGTACCATTCT[C/T]AGTTCAGTGGGAAAG | 10451 |
rs72703590 | snp | C/T | 0.0741063 | 0.177655 | intron-variant | VAV3 | GRCh38.p7 | 1:107640207 | ATAGCCAAAAACTAG[C/T]GGCAACCTGAAAGTC | 10451 |
rs72703592 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107648075 | CAATTTGGTGGAAAA[A/C]AAACTGGTCTAAAGA | 10451 |
rs72703593 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107648900 | ATGATCTGAGTACCC[A/G]CCACATGTCTGGTGT | 10451 |
rs72703595 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107651310 | TTTTAAGTGCCTTAA[A/G]CATACACTCCTTTAG | 10451 |
rs72703598 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107662541 | ATGTTTTTAGAGGCC[C/T]AATAGTTATCTTTTC | 10451 |
rs72703602 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107666568 | ATGGCAAGATCATTT[C/G]AGACTTTTTTTTTTT | 10451 |
rs72705616 | snp | C/T | 0.381308 | 0.21274 | intron-variant | VAV3 | GRCh38.p7 | 1:107694238 | AGGTACGGTTAATGA[C/T]TGGCAAAGAGTTTGG | 10451 |
rs72705619 | snp | A/G | 0.49823 | 0.0296997 | intron-variant | VAV3 | GRCh38.p7 | 1:107701370 | CGTTGGCCCCTTTTC[A/G]CCATGGCTGGAGCAG | 10451 |
rs72705622 | snp | C/G | 0.234982 | 0.249549 | intron-variant | VAV3 | GRCh38.p7 | 1:107709929 | CAGTGTGAGAACAGA[C/G]GAATACAATATTTTT | 10451 |
rs72705627 | snp | A/T | 0.213937 | 0.247385 | intron-variant | VAV3 | GRCh38.p7 | 1:107724998 | CTCTAGCAGCCATGC[A/T]GAAGGGGTGAGGTGA | 10451 |
rs72705628 | snp | C/G | 0.145642 | 0.227177 | intron-variant | VAV3 | GRCh38.p7 | 1:107726506 | TAATCAATCAATTAT[C/G]TACATAATAACGCTC | 10451 |
rs72705632 | snp | A/G | 0.429238 | 0.174281 | intron-variant | VAV3 | GRCh38.p7 | 1:107735678 | GCTGAATTCCTGAAT[A/G]GACCAATAACAGGCT | 10451 |
rs72705636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739314 | TCCGGATCAAACAGG[A/C]TATTGAAAGACTCCA | 10451 |
rs72705642 | snp | G/T | 0.209693 | 0.246729 | intron-variant | VAV3 | GRCh38.p7 | 1:107746647 | CCTACCTAGAATAAA[G/T]GTTTTATTTGCCAGC | 10451 |
rs72705643 | snp | A/G | 0.181022 | 0.240296 | intron-variant | VAV3 | GRCh38.p7 | 1:107746804 | ACCTAGAGCTCTAGC[A/G]GCTATCTCAGACTAC | 10451 |
rs72705644 | snp | C/G | 0.209388 | 0.246679 | intron-variant | VAV3 | GRCh38.p7 | 1:107750077 | ATGCTGGGAAGGTAT[C/G]ATTGCCATCTTCATT | 10451 |
rs72705645 | snp | A/G | 0.150667 | 0.229419 | intron-variant | VAV3 | GRCh38.p7 | 1:107750181 | ACAGGATTCACAAAC[A/G]GGTCTAATTTTGGAA | 10451 |
rs72705655 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764290 | TCTCATCTGTCAAAG[C/T]TCATCCCATTCTTTG | 10451 |
rs72705667 | snp | A/G | 0.192715 | 0.243348 | intron-variant | VAV3 | GRCh38.p7 | 1:107788698 | AGTTTTCTAGATAGA[A/G]ATATTCCCTGCTCTG | 10451 |
rs72705676 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | VAV3 | GRCh38.p7 | 1:107804716 | TCTGGGGCTGTATCC[A/G]AACTTCAGTTTTACC | 10451 |
rs72705684 | snp | C/T | 0.030665 | 0.119967 | intron-variant | VAV3 | GRCh38.p7 | 1:107821976 | CTTTTAAAGAGAAAT[C/T]GCATGCAGGGGAGGA | 10451 |
rs72707741 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107828493 | TTAAGCCAGTGAGAC[A/G]CATGTTGAATTTTTG | 10451 |
rs72707743 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107842356 | GAGTGGCCCAGGAGT[C/G]AACAGCTGACTCAAG | 10451 |
rs72707744 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | VAV3 | GRCh38.p7 | 1:107851096 | ATGAACAAAGAAGCC[A/G]GCCCTCCGGAGCTTG | 10451 |
rs72971543 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591095 | GAACCTTCACACAAA[C/T]GACCTCTTTGCTATG | 10451 |
rs72971552 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107597719 | GCTAAAAGCAGCATA[A/G]TTTGGCTAAAGCATT | 10451 |
rs72971564 | snp | C/T | 0.252421 | 0.249988 | intron-variant | VAV3 | GRCh38.p7 | 1:107606580 | GGGTCAACAGTCTAG[C/T]TTCCATATAGCTTCT | 10451 |
rs72971574 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107612874 | CATAAGGTTTCTATC[C/T]GAATTTTAGCTACCC | 10451 |
rs72971584 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107618636 | TGCTATGATCCTTTA[G/T]GGTAGGTCCAATTAC | 10451 |
rs72971589 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107619321 | AAGAAACGATCAGGA[A/G]AGAGAGGAATCAGAG | 10451 |
rs72973668 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107626561 | TCTGCCTTGGCTTCT[A/G]CTGATTTTACTCAAG | 10451 |
rs72973675 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107627952 | GAACTGAGATAAAGT[A/T]ATGAAACCCATAGCT | 10451 |
rs72973699 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107632167 | CTGGTGAGCTGGGGA[C/T]AGTGTCAAAATTACC | 10451 |
rs72975624 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107643498 | CAATACTGGTCACAA[C/T]GGACAACCTCACAGT | 10451 |
rs72975632 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | VAV3 | GRCh38.p7 | 1:107646831 | AATAAAACTAAAGCT[A/T]CATGTAGGTATGCAG | 10451 |
rs72975640 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | VAV3 | GRCh38.p7 | 1:107651417 | ATAGCACCTTTTTTT[G/T]GTGTCTTCGTACAGA | 10451 |
rs72975642 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107656573 | GTTAACATTAATCCA[C/T]TGCATATTTCAAAAT | 10451 |
rs72975648 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | VAV3 | GRCh38.p7 | 1:107660340 | TATAATTGTTATTTT[A/C]ATCTTAATTATCCAA | 10451 |
rs72975650 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | VAV3 | GRCh38.p7 | 1:107660506 | AGGCCAAGGCAGACC[A/T]CTGGCCTTATAGCCT | 10451 |
rs72975651 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107660741 | TTTTCTGCTTGGAAT[C/G]TGAACAACATAATAA | 10451 |
rs72975659 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107664437 | TTCCTACTTATAAGT[A/G]AGAACTACAGTGCTT | 10451 |
rs72975665 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107665914 | ACAAACGGTGAAGGA[C/T]ATTATCTGTAAATGC | 10451 |
rs72975669 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | VAV3 | GRCh38.p7 | 1:107667498 | GCCTAGGAAATGAGA[C/T]GCAATTTTTACACAA | 10451 |
rs72975670 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107667964 | CCAACTGGGCCCTTC[C/T]GAGAAGCTCTTTCCC | 10451 |
rs72975682 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107676128 | ATCTGCTAAAACCAA[C/G]CCTCTCTTTCCTCTC | 10451 |
rs72975691 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107680078 | ACAATTATTAATAGG[A/G]AGTGAATGATTTAAA | 10451 |
rs72977603 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107684133 | ATTATAGAAAATGAA[C/T]CTGTAAGAAAACAAC | 10451 |
rs72977607 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107684895 | ATAATTTAGAGGAAC[C/T]CTATATAAACAACAT | 10451 |
rs72977609 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107684995 | TACATATCCCATCAT[C/T]TTCTTAATGCACAAT | 10451 |
rs72977612 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107685808 | ATTTGTCATTCTGTC[A/G]TCTCTATGCGTATAC | 10451 |
rs72977615 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107692079 | TGCCTATCTCAACAG[A/G]GGCCACAGAAAAGTA | 10451 |
rs72977619 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107692348 | AGGAATACAACCATA[A/T]AATAGATTCCAATTC | 10451 |
rs72977656 | snp | G/T | 0.00564939 | 0.0528468 | intron-variant | VAV3 | GRCh38.p7 | 1:107704503 | TTATGTTTAGCAAAT[G/T]TTATGTCCTCATTAA | 10451 |
rs72977659 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107704763 | TTCAAGGTACCCCCT[C/T]GGTAGAGGGAGACGA | 10451 |
rs72977662 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107705551 | TAAAATAAAGCATTA[A/G]TGTGAACATTAAAAA | 10451 |
rs72977667 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107705780 | ATCCTAACTGCCTGG[A/C]ACGAATAATATCACT | 10451 |
rs72977669 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107705949 | CATATTAAAATAATC[A/G]AATTTTTGTACTTAG | 10451 |
rs72977671 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107706261 | CACACAGAATCCTGG[C/T]GAAATGAAGCATAAC | 10451 |
rs72977672 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107706299 | GGCGACCAGGCATCA[A/G]TCTCTGAGGTACCAG | 10451 |
rs72977673 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107706761 | CAAGGTGATAGGGTC[A/G]TAGATGATTTGTCAA | 10451 |
rs72977674 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107707690 | AGTGTAAGAGGGTAA[C/T]TCAAGAGATTACATG | 10451 |
rs72977675 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107707801 | GGCCTGTGGGGGTGC[C/T]GAAACCAAAGACAGT | 10451 |
rs72977676 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107707828 | CAGTAAGCTGGCTGG[A/G]TGAGAAGGGTTGGGA | 10451 |
rs72977679 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107708143 | GATAGGTTGGCAGGG[A/G]CCAAGGAAAGAAGTG | 10451 |
rs72977680 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107708687 | ATCTCAAATGCAGCA[C/T]ATACAAAACTCAACT | 10451 |
rs72977684 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107709088 | CTGAAATTCAGATAC[A/G]TCAGCCTCCATAACA | 10451 |
rs72977685 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107709652 | ACCAGGTGGAGATAA[C/T]TGAATCGTGGGGATG | 10451 |
rs72979630 | snp | C/T | 0.0543475 | 0.155628 | intron-variant | VAV3 | GRCh38.p7 | 1:107731638 | AAATCTTCTTCATTA[C/T]AAGGAAGAATCTTCT | 10451 |
rs72979631 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | VAV3 | GRCh38.p7 | 1:107732638 | CCGAGATTGAGCTGC[A/G]AGGCGGCAGACTGGC | 10451 |
rs72979637 | snp | A/G | 0.0618563 | 0.164627 | intron-variant | VAV3 | GRCh38.p7 | 1:107739167 | GTTCAAGAATGCCAA[A/G]AAGTATCAAATACAT | 10451 |
rs72979639 | snp | G/T | 0.0618563 | 0.164627 | intron-variant | VAV3 | GRCh38.p7 | 1:107739214 | GAAAAATGAGAGAGC[G/T]TGATCCTCACTAGGC | 10451 |
rs72979640 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107742210 | ATATTTTGCCACACA[A/G]TAAGAATGCCACAAC | 10451 |
rs72979644 | snp | A/G | 0.0558544 | 0.157504 | intron-variant | VAV3 | GRCh38.p7 | 1:107743406 | GGGGCTGTATCAAGC[A/G]TAATTCTTGGGACTC | 10451 |
rs72979653 | snp | C/G | 0.017161 | 0.09103 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755379 | CAACTCCTAGAATGT[C/G]GTTGATGTGGGGGTG | 10451 |
rs72979658 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107757625 | GATTCCATAATGATT[A/G]AAATCACACTTTTTA | 10451 |
rs72979665 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107759571 | AAACATTTCTAGAAT[G/T]TTTACCTATGTGTAG | 10451 |
rs72979668 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107760730 | GTTGATGCTTCATTA[A/G]TATTTTGTTGAGTGA | 10451 |
rs72979677 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107762599 | CATTTTAAGGCCCTT[G/T]GAATTAAGGTTGTAG | 10451 |
rs72979685 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107767837 | TGGGCAAATATCCTT[C/T]TAAGATTGTAAGATT | 10451 |
rs72979687 | snp | C/T | 0.00320877 | 0.039926 | intron-variant | VAV3 | GRCh38.p7 | 1:107768532 | GAAAGAAGAAGAAAA[C/T]AGTAATTAAGTATAA | 10451 |
rs72979688 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107768784 | AGGAAGAAAAGAACA[C/T]TATTGTCTGAGTTGC | 10451 |
rs72981405 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107782486 | AACAAGCTGAGACCA[A/G]CTCCTATTTTCTGCT | 10451 |
rs72981414 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107783460 | TGCTCTGTGAGGGCT[A/G]AGGGAAGAAGAACCC | 10451 |
rs72981417 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107784362 | TAACATTTCAGTGTA[C/T]ATAAACAGCAATGAT | 10451 |
rs72981424 | snp | C/T | 0.00795532 | 0.062565 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787211 | CTGTCCTGGTTATTG[C/T]TCTTTCCACTTCACT | 10451 |
rs72981429 | snp | C/G/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107788756 | GTGTTAAACTTAGTA[C/G/T]GCAAATGATAAAGAA | 10451 |
rs72981433 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107791060 | GCTGAGTTCTATACA[A/T]CGATAGTCTCACCAA | 10451 |
rs72981442 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107795247 | AGAAATATTTTTAAA[C/T]GGACGAAGTTACCAA | 10451 |
rs72981443 | snp | C/T | 0.0539704 | 0.155153 | intron-variant | VAV3 | GRCh38.p7 | 1:107795564 | TGCCCTGTCAAAATA[C/T]GGCATATGTAAGATG | 10451 |
rs72981458 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107824849 | TAGAAATAATATAAA[A/C]ATATAAAAAGCAATA | 10451 |
rs72981460 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107826600 | AGTTCACTGGCAGAC[A/G]GTTGGCAAACTGATG | 10451 |
rs72981461 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107829822 | ATGTCAAAAGAGATC[A/G]CAGATTTGCTCCATA | 10451 |
rs72981464 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107830017 | GTTAATGAGCAAAAC[A/T]ACTTAAAACTCCTTA | 10451 |
rs72981496 | snp | G/T | 0.0460142 | 0.144533 | intron-variant | VAV3 | GRCh38.p7 | 1:107874703 | GCTAATTTTTTGGTG[G/T]TGTTGTTGTATGTGT | 10451 |
rs72983421 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894663 | CTAATAATTCTTAAC[G/T]TTTAAAAACGGCAGA | 10451 |
rs72983424 | snp | A/G | 0.0524604 | 0.153226 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895251 | ATGGGACGTGAGTGG[A/G]GAACAAAAATCAATA | 10451 |
rs72983425 | snp | A/G | 0.116138 | 0.211142 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895495 | CATTTTACAGATGAG[A/G]AAACAGAGGTAGAGA | 10451 |
rs72983428 | snp | A/T | 0.084728 | 0.187577 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895625 | CTAAACACCTCACTA[A/T]GCCTTTAGACTACCC | 10451 |
rs72983443 | snp | G/T | 0.0905309 | 0.192535 | intron-variant | VAV3 | GRCh38.p7 | 1:107901481 | TGGATATTCAGCAGA[G/T]GCAGTGGTTAACAAC | 10451 |
rs72983446 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107903589 | GTGGCAAAGACAGTA[A/G]TAAGGGCATTCACCT | 10451 |
rs72983447 | snp | C/G | 0.0648419 | 0.167978 | intron-variant | VAV3 | GRCh38.p7 | 1:107905008 | TTCCAGATAGAAGAA[C/G]AACCCAGTGCAAAGC | 10451 |
rs72983448 | snp | A/G | 0.0648419 | 0.167978 | intron-variant | VAV3 | GRCh38.p7 | 1:107905072 | AATATCAAGGAGCCA[A/G]GGTGGCTTGAGAAGT | 10451 |
rs72983453 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107908238 | TTCTTCCCCCAGCAG[C/T]GGCTGGTAGAAGTGG | 10451 |
rs72983459 | snp | A/T | 0.0858192 | 0.188533 | intron-variant | VAV3 | GRCh38.p7 | 1:107911441 | AGAATAAAAATGCTG[A/T]GTCTCCCATAAACAC | 10451 |
rs72983462 | snp | A/T | 0.0644693 | 0.167566 | intron-variant | VAV3 | GRCh38.p7 | 1:107913793 | TCACAAATTATTATT[A/T]TTTTTAATTATTATT | 10451 |
rs72983466 | snp | C/T | 0.084364 | 0.187256 | intron-variant | VAV3 | GRCh38.p7 | 1:107914776 | GTCCTATAGCCAGCA[C/T]TGTACTAAATACTGT | 10451 |
rs72983471 | snp | A/G | 0.084364 | 0.187256 | intron-variant | VAV3 | GRCh38.p7 | 1:107915028 | ACAGCCTAAAGACAG[A/G]TATAAAGGTAGGAAT | 10451 |
rs72983491 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | VAV3 | GRCh38.p7 | 1:107926701 | ATCACAGCAGAAATC[C/T]AAACCAGGCTGAACT | 10451 |
rs72983494 | snp | A/T | 0.0520825 | 0.152737 | intron-variant | VAV3 | GRCh38.p7 | 1:107931032 | TCCTGATCTCGTTAC[A/T]ACCTAGAGAAAAGGA | 10451 |
rs72983497 | snp | G/T | 0.0821764 | 0.185298 | intron-variant | VAV3 | GRCh38.p7 | 1:107931193 | GACTGTATGTTAGAT[G/T]ATAATAAGAAATTGC | 10451 |
rs72983499 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | VAV3 | GRCh38.p7 | 1:107931353 | AATAATAATTATACA[C/T]TGAATACATGTATCA | 10451 |
rs72985403 | snp | A/G | 0.0501905 | 0.150254 | intron-variant | VAV3 | GRCh38.p7 | 1:107932246 | CAAGTTCAAGAGCGG[A/G]CATTAAGACATACTT | 10451 |
rs72985406 | snp | C/T | 0.0818113 | 0.184966 | intron-variant | VAV3 | GRCh38.p7 | 1:107935459 | TCTCCTACAGTGTTA[C/T]GAGCACTGAAATGTT | 10451 |
rs72985409 | snp | C/G | 0.0818113 | 0.184966 | intron-variant | VAV3 | GRCh38.p7 | 1:107937770 | CTCTGGTTAAGGCTT[C/G]TAGTCCCAATTATTA | 10451 |
rs72985413 | snp | A/G | 0.14933 | 0.228835 | intron-variant | VAV3 | GRCh38.p7 | 1:107938040 | ACTCTGTCACACAGA[A/G]CATGTCTGCAGTCTT | 10451 |
rs72985422 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | VAV3 | GRCh38.p7 | 1:107945121 | GGATGGTTTAGGTAA[C/T]GTTATTATAGGGCTT | 10451 |
rs72985442 | snp | A/G | 0.218151 | 0.247963 | intron-variant | VAV3 | GRCh38.p7 | 1:107952723 | TATGAAGTAAAACCC[A/G]TACTGTATAGACTAA | 10451 |
rs72985445 | snp | G/T | 0.217551 | 0.247885 | intron-variant | VAV3 | GRCh38.p7 | 1:107952811 | ACAAAGTCCAACATT[G/T]AGCAGACAATGTGAT | 10451 |
rs72985448 | snp | A/T | 0.212728 | 0.247206 | intron-variant | VAV3 | GRCh38.p7 | 1:107952939 | AAACTAATCAGACTA[A/T]AAAATAACAGAAATT | 10451 |
rs72985449 | snp | G/T | 0.236434 | 0.249632 | intron-variant | VAV3 | GRCh38.p7 | 1:107953660 | CCTGTCAGAGACAGA[G/T]CTGGGACTAGAACCC | 10451 |
rs72985452 | snp | G/T | 0.217851 | 0.247924 | intron-variant | VAV3 | GRCh38.p7 | 1:107953960 | CTTGTAACACAGATT[G/T]TGAAAGCACATTCAG | 10451 |
rs72985456 | snp | C/T | 0.0685596 | 0.171987 | intron-variant | VAV3 | GRCh38.p7 | 1:107954230 | AATAGAAAAAAAATG[C/T]CCTATCAAAGCACAT | 10451 |
rs72985459 | snp | G/T | 0.235854 | 0.249599 | intron-variant | VAV3 | GRCh38.p7 | 1:107954815 | GTTCACATTCAGATA[G/T]GCCGATAGCCTCGCT | 10451 |
rs72985462 | snp | A/C | 0.272241 | 0.249009 | intron-variant | VAV3 | GRCh38.p7 | 1:107956896 | GGACAAATCGAGGGA[A/C]GTCAAGGAATTATAA | 10451 |
rs72985464 | snp | A/C | 0.206947 | 0.246265 | intron-variant | VAV3 | GRCh38.p7 | 1:107956961 | GAAAACTGAATCAGG[A/C]AGTTAAGAGGTGGTA | 10451 |
rs72985466 | snp | C/T | 0.067446 | 0.170804 | intron-variant | VAV3 | GRCh38.p7 | 1:107956965 | ACTGAATCAGGAAGT[C/T]AAGAGGTGGTAGAAG | 10451 |
rs72985478 | snp | A/C/T | 0.067446 | 0.170804 | intron-variant | VAV3 | GRCh38.p7 | 1:107960432 | GATCAGGCCACTGCA[A/C/T]GCCAACTTGGGCTAC | 10451 |
rs72985480 | snp | A/G | 0.225893 | 0.248835 | intron-variant | VAV3 | GRCh38.p7 | 1:107961136 | TGAATTATTCATTTA[A/G]ACAATTCAAAGTTTA | 10451 |
rs72985484 | snp | A/C | 0.226188 | 0.248863 | intron-variant | VAV3 | GRCh38.p7 | 1:107961187 | CACTAAACTCATTGA[A/C]TGTATTACCCCTACT | 10451 |
rs72985487 | snp | A/C | 0.21725 | 0.247846 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962531 | GTTGTTTCATAAAAT[A/C]ATTTCATAAGTCTCA | 10451 |
rs72985489 | snp | A/G | 0.225005 | 0.248747 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962932 | GCTACCCCCACTAGG[A/G]AACAGAACTCTTAGA | 10451 |
rs74108928 | snp | A/T | 0.499732 | 0.0115784 | intron-variant | VAV3 | GRCh38.p7 | 1:107796804 | GTAAAAAAAAAAAAA[A/T]ATATATATATATATG | 10451 |
rs74109105 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107611211 | AAAAAGTTTGGACTT[C/T]AGAGCATTTCAGATG | 10451 |
rs74109106 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107612848 | AATCTGGTTCTTTAA[G/T]CCAGAAATACCATAA | 10451 |
rs74109111 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107636433 | TCCTTGACTTATAAT[A/G]GGGTTATGCCCTGAT | 10451 |
rs74109199 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107714998 | GAAATGTAAAGTCAG[A/T]TAAATCTATAATAAA | 10451 |
rs74109656 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107911136 | AACTTCTAATAGCAC[A/G]TAAGGTTAGAAATTT | 10451 |
rs74109676 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107917125 | GAAGAGAAGGAAATA[A/G]TCAAAATCTACTGGT | 10451 |
rs74109680 | snp | A/G | 0.0944967 | 0.195752 | intron-variant | VAV3 | GRCh38.p7 | 1:107927534 | GCTCTGGACCTGCCC[A/G]GCAACAGAGAGCCCA | 10451 |
rs74109682 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107938211 | TACAGAAGAGGAGGC[A/G]ATCCCCGAGCCAGAA | 10451 |
rs74109684 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107944043 | GTCATTTGCCTGTAG[A/G]CTAGGCTGCCATAAG | 10451 |
rs74109685 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107944469 | GTGTATCCTCCAAAA[C/T]ATACCTCTCTTATAA | 10451 |
rs74109687 | snp | C/T | 0.359998 | 0.2245 | intron-variant | VAV3 | GRCh38.p7 | 1:107952487 | ATATATATATATATA[C/T]ACACATAAATTCAAC | 10451 |
rs74109905 | snp | C/T | 0.206947 | 0.246265 | intron-variant | VAV3 | GRCh38.p7 | 1:107957134 | GAATGTGTTCCCTTT[C/T]TCACTAAAATGTGCC | 10451 |
rs74110010 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964274 | CAAAGCAAAAGAAGA[A/G]ACTAAAGGCAAATTA | 10451 |
rs74111051 | snp | C/T | 0.0205511 | 0.0992634 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571877 | GTTCTGGCACCCAGA[C/T]GGATTGATGAGAGGG | 10451 |
rs74111054 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589894 | GTTAAGGAATTATTA[G/T]GATGTTTAAGGAATT | 10451 |
rs74111415 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | VAV3 | GRCh38.p7 | 1:107746011 | TCATGGATGCTGCAG[A/G]AGTTATTTTCTTTTA | 10451 |
rs74225262 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107805140 | TGCTTCTTGGTAAAG[C/T]CTTATTGGGGTTGAA | 10451 |
rs74262708 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107799324 | ATCAAAAAAAAAAAA[-/AA]GACACCAGGTTCTAT | 10451 |
rs74262709 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107851413 | AAAAAAAAAAAAAAA[-/AA]GCAAATTTTTGTTTC | 10451 |
rs74307664 | in-del | -/GTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107750016 | TGCCTTGAGARKTGT[-/GTT]TSATCCCTTTCACAA | 10451 |
rs74336880 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | VAV3 | GRCh38.p7 | 1:107776548 | GGCTAAAACAAGCCC[A/G]GTGTGTTGGGTGTAT | 10451 |
rs74344389 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107865847 | CCACTTCCTGATGGT[C/T]CACACCTGTTGCACT | 10451 |
rs74346298 | snp | G/T | 0.030665 | 0.119967 | intron-variant | VAV3 | GRCh38.p7 | 1:107664739 | AATGTTGTCATGGGA[G/T]AGGGACCCACAATGC | 10451 |
rs74370816 | snp | A/T | 0 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570978 | CGGCCCTCCTACTAG[A/T]CGCATAGCGTCCACG | 10451 |
rs74384451 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107882144 | AGCTTATTGTGAGAT[G/T]AGTTATTTCAGTCCC | 10451 |
rs74391337 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107770732 | TTCTGGACATTTCTG[C/T]AGTTAGAATTATCAA | 10451 |
rs74399981 | snp | A/C | 0.296873 | 0.245566 | intron-variant | VAV3 | GRCh38.p7 | 1:107836535 | AAAAACAAGAACAAA[A/C]CAAGCTCAAAACTAG | 10451 |
rs74439054 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857548 | AGGAACAATGGAGGA[C/T]ATGAAACATGGAAAA | 10451 |
rs74439495 | snp | A/T | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107805104 | ATCCTTTCTTTGTCC[A/T]TGACCTTTGAGAGTT | 10451 |
rs74457985 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107953530 | AATGCTGCCTTGATA[C/T]GTGTAAAACATTTTA | 10451 |
rs74461618 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | VAV3 | GRCh38.p7 | 1:107812450 | ATCATTTTTTAAGCT[G/T]ATTTCCAAAGAATAG | 10451 |
rs74465382 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | VAV3 | GRCh38.p7 | 1:107792513 | ATAAATTTCAACAGG[C/T]AATAAAGCCACTAGT | 10451 |
rs74486046 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107902339 | GATGGAGATGTAATT[C/G]TTTCAATTTTTTTTA | 10451 |
rs74488489 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107882312 | TCTCAGAATAAAGAA[A/G]TTCTCAGTAGGACAC | 10451 |
rs74491349 | snp | C/T | 0.110519 | 0.207473 | intron-variant | VAV3 | GRCh38.p7 | 1:107929648 | CAGTACAATAAGATA[C/T]AAACAGAAATAATAA | 10451 |
rs74491891 | snp | C/T | 0.163236 | 0.234461 | intron-variant | VAV3 | GRCh38.p7 | 1:107843235 | CTCTTAAACACACAT[C/T]CTGAGTAAGTTTCCT | 10451 |
rs74512414 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107852198 | GGGACTATATATTTT[C/T]CCCTTATGAGGATGA | 10451 |
rs74530482 | snp | C/G | 0 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570999 | AGCGTCCACGGGGCT[C/G]GCGGGCGGGGGGGTG | 10451 |
rs74532087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107741075 | GGACTAGCAGTACTC[A/G]TAGCGGTAGTAGTTG | 10451 |
rs74533693 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107684244 | CTAAAGCATTAAACT[A/C]ATTCCCACCTAACTA | 10451 |
rs74534664 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107940474 | GGACATTTGAAAGAT[A/T]GAGAAGGTTCTACAA | 10451 |
rs74581961 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107810467 | ATACTCTATTTATAT[C/T]TATAACTAAAGAAAT | 10451 |
rs74605298 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107855181 | TATAATCTGCCTATG[C/T]ACCCCAAAACAAGAA | 10451 |
rs74608279 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107931609 | TTTACATATTTTAGA[C/T]TATCCATGGATATTA | 10451 |
rs74614887 | snp | C/T | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107822173 | TGGGTGAGAGTTCCA[C/T]AGTGGGCATGCTTTG | 10451 |
rs74618898 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107610949 | AGTATTTCAGAGAAC[C/T]AGCCAATGTGAACAT | 10451 |
rs74638822 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107852660 | CTATTGAATGGTTGT[C/T]AGTTTTTATTCCAAA | 10451 |
rs74641750 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | VAV3 | GRCh38.p7 | 1:107809697 | CTATGCAAAGGCACT[A/G]CACTGTGCAAATTAC | 10451 |
rs74652641 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107879721 | TTTGACAAAAAAAAA[-/AA]TTGTACAACTTTGCT | 10451 |
rs74673465 | snp | C/T | 0.00178644 | 0.0298333 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107669369 | AACCTCAAGGCTGCA[C/T]TTTCACCCATGTCCT | 10451 |
rs74676442 | in-del | -/ATGAGC | 0.227959 | 0.249026 | intron-variant | VAV3 | GRCh38.p7 | 1:107832041 | AACAACAAGATGAGC[-/ATGAGC]TTGGAAGCAAATGCA | 10451 |
rs74678088 | snp | A/C | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107815175 | GCATGAATAGTGTCT[A/C]TCTTAGGAAGAAAAT | 10451 |
rs74682295 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | VAV3 | GRCh38.p7 | 1:107712941 | AGGTGGAAAGCAAGA[G/T]GAAGAATTTCGGGAC | 10451 |
rs74683142 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | VAV3 | GRCh38.p7 | 1:107692849 | ACTAAAGGAAAAGAT[A/G]CATTATACCAAAGTC | 10451 |
rs74691032 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107608070 | AAAGAAAAGTAATTT[A/T]AAATTCTACTACATC | 10451 |
rs74714642 | snp | A/G | 0.243919 | 0.249926 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592606 | ACAACTTTTCCTAAT[A/G]CACCAATCTGTTAAC | 10451 |
rs74761768 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107909310 | ACCTCACAGCTCTTC[A/C]AGCTACTCCAAAAGC | 10451 |
rs74761871 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107747925 | TAGTTTACATTAACA[C/G/T]GAGCATTTCTTAAAA | 10451 |
rs74773734 | snp | C/T | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570749 | GGACTCCCTTTCGAT[C/T]GGCTGAGGGCAACAG | 10451 |
rs74776274 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107923560 | TCACAGTTTTGCATG[G/T]CTGAGGAGGCCTCAG | 10451 |
rs74808790 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107904292 | ACTCTAGATAAATGT[A/G]TACGTATGATGTGAC | 10451 |
rs74810481 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107586142 | TCCCTTGGCATAGTT[G/T]TTTTTTTTTTTTTTT | 10451 |
rs74813960 | snp | A/G | 0.074958 | 0.178495 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570869 | TCCACTTCGGCCTTT[A/G]AAGTTCTCTTTAGAA | 10451 |
rs74817473 | snp | A/G | 0.176861 | 0.239062 | intron-variant | VAV3 | GRCh38.p7 | 1:107656379 | AGAAAGACAAATATT[A/G]CATGTTCTCCCTCCT | 10451 |
rs74820090 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107804588 | TTTACACATTTTTGT[A/G]TTGACTATCTCAACA | 10451 |
rs74829019 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107706153 | AAAATGATATGCTCC[A/G]AGACGTTACACGCAA | 10451 |
rs74839344 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107918107 | TCCAATAGCTTTCAG[A/G]CTGGCCAAAAGGAAG | 10451 |
rs74850298 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922974 | AAAARAAAAAAAAAA[-/A]AAAAGAGCACAATTT | 10451 |
rs74850908 | snp | A/G | 0.110167 | 0.207236 | intron-variant | VAV3 | GRCh38.p7 | 1:107925659 | AAAAGTAGAATGGTG[A/G]CTGTCAATGGCTAGG | 10451 |
rs74851734 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107880814 | AAAAAAAAAAGAAAA[A/G]AAAAAAAGCACCAAA | 10451 |
rs74881114 | in-del | -/CTGTGTGTGTG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624374 | ATTATAGTCTTATGA[-/CTGTGTGTGTG]TGTGTGTGTGTGTGT | 10451 |
rs74905335 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107955549 | AAGAAATGCTGCATT[C/T]TACCAGACACTGTGG | 10451 |
rs74906382 | snp | A/T | 0.046775 | 0.145601 | intron-variant | VAV3 | GRCh38.p7 | 1:107828261 | TTGTTTCTGCCTTTC[A/T]AGCGTACAAGATTCA | 10451 |
rs74926667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107828224 | CTGTTCTTGCGTTAA[A/G]TATCGAGGAAGAAGA | 10451 |
rs74931935 | snp | A/G | 0.247905 | 0.249991 | intron-variant | VAV3 | GRCh38.p7 | 1:107626025 | ACCCTGCAGGAAAAA[A/G]AAAGAGATAATACTT | 10451 |
rs74946308 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107792564 | GGCCCATTACATAAT[A/T]GTGTTAATTACTTAA | 10451 |
rs74951970 | snp | C/G | 0.0322114 | 0.122752 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786996 | ACACACACACATACA[C/G]ACATACACACACAAA | 10451 |
rs74992728 | snp | A/G | 0.107694 | 0.205546 | intron-variant | VAV3 | GRCh38.p7 | 1:107653261 | TTAAAGAGGCTATGG[A/G]GCCCTTAGCTCAGAG | 10451 |
rs75003314 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107771268 | CTTTTTTTTTTTTTT[G/T]TTGAGTCAGAGTCTC | 10451 |
rs75013860 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107793261 | ATCATGGGTGATCTG[C/T]CCCAGAGTGTGTAAC | 10451 |
rs75033187 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | VAV3 | GRCh38.p7 | 1:107780194 | ATAATAATAGTTAGA[C/T]TATTAACAATCATTA | 10451 |
rs75033347 | snp | C/T | 0.109814 | 0.206997 | intron-variant | VAV3 | GRCh38.p7 | 1:107953122 | GCAGGAACGGGAAAC[C/T]TCACCGAATCTGGAA | 10451 |
rs75037455 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | VAV3 | GRCh38.p7 | 1:107901075 | GGACTGTAAATATAA[A/G]TCGGACCACCATGGA | 10451 |
rs75059947 | in-del | -/A | 0.0711525 | 0.174681 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896742 | GATATAATCTGTATT[-/A]AAAAAATGGCTACAG | 10451 |
rs75072520 | snp | G/T | 0.108048 | 0.20579 | intron-variant | VAV3 | GRCh38.p7 | 1:107929706 | AAAAAGTGTAGAAAT[G/T]TATTAGTTTTCTTTT | 10451 |
rs75073082 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107761460 | AAATCATGGCCCCCC[A/C]GGGTCTTCTTCAGTT | 10451 |
rs75097907 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107891355 | TACCAAATTCTATAC[C/T]AACAGAATTCAGGTT | 10451 |
rs75107555 | snp | C/T | 0.0785177 | 0.181917 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963365 | ACAACTCTGAAGGGG[C/T]ACCGAGAGGTAGCAA | 10451 |
rs75110713 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107867748 | AGGCTGAGCCAGCTC[C/T]AGGCTGGAAGCTGGC | 10451 |
rs75123433 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107791396 | TATCAAAAAAAAAAA[A/G]AGACTGCTGCAATAG | 10451 |
rs75125154 | snp | A/G | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107820904 | TTCTTTAATACCTAT[A/G]TAACCAAGAGAAAAG | 10451 |
rs75150159 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107880797 | TGAGATTCTGTCTCC[A/C]AAAAAAAAAAAGAAA | 10451 |
rs75156214 | snp | A/G | 0.178144 | 0.239451 | intron-variant | VAV3 | GRCh38.p7 | 1:107628582 | CTTTTTATTTTCTGT[A/G]TGACTCTTCCTGTTA | 10451 |
rs75159251 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107675553 | TTAAAAAGATCTCTC[A/C]TTCTCTTTCTTTCCT | 10451 |
rs75180432 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107906680 | CAAAAAAATTAAAAT[A/C]CAATACAATACAATA | 10451 |
rs75204344 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107645024 | TAGCTTTTCTAGTCC[C/T]ACTTATTCCTAAGTT | 10451 |
rs75237583 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107639951 | TAAAAAAAAAAAAAA[A/G]AGAATGACCACACCA | 10451 |
rs75244903 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858285 | ACATATTGACAGCAC[A/T]GAAATTATACAAGAT | 10451 |
rs75251232 | snp | A/C | 0.498652 | 0.0259235 | intron-variant | VAV3 | GRCh38.p7 | 1:107701355 | ACAGCCTGAGCTGTA[A/C]GTTGGCCCCTTTTCG | 10451 |
rs75276122 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107826411 | CTTAGGGAGTCATCA[A/G]CCCTTCCAAGTTGAG | 10451 |
rs75292044 | snp | A/C | 0.0718919 | 0.175435 | intron-variant | VAV3 | GRCh38.p7 | 1:107842394 | AACTGCAGTCCTTCC[A/C]ACTGATTTTTAGTAC | 10451 |
rs75292063 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107677972 | CAACCAAGAAAGATG[A/C/T]GAGCAAGAGGCTGTG | 10451 |
rs75303797 | snp | A/C | 0.0722614 | 0.17581 | intron-variant | VAV3 | GRCh38.p7 | 1:107834493 | TACTGTCAATTAGAT[A/C]AAGTTATTTGATAAC | 10451 |
rs75308083 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | VAV3 | GRCh38.p7 | 1:107888872 | ATTGATATTCTTTCT[C/T]GGCACGCACACTCCT | 10451 |
rs75317139 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | VAV3 | GRCh38.p7 | 1:107956897 | GACAAATCGAGGGAC[A/G]TCAAGGAATTATAAT | 10451 |
rs75321380 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107842056 | TCTATACTACCATTG[C/T]TCATGCCCCAAATTA | 10451 |
rs75323755 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107681668 | ACTTTTTTTTTTTTT[G/T]TTTTGAGACAGAGTC | 10451 |
rs75328924 | in-del | -/CAAAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107682719 | GATAGGAAAACAAAA[-/CAAAA]TGAAACACATAGTCC | 10451 |
rs75329226 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107597915 | TAAGGCCCATTTCAT[G/T]ATGTTCTTGAGTGAA | 10451 |
rs75335758 | in-del | -/GGTCAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107608161 | AATATTATTCTAACT[-/GGTCAT]ATTTTCAGTAGGATT | 10451 |
rs75343376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107816724 | ATAATTTGGAAAATA[C/T]AAAATGTACACAAAA | 10451 |
rs75363405 | snp | A/G | 0.110167 | 0.207236 | intron-variant | VAV3 | GRCh38.p7 | 1:107946549 | TGACCTAGAAATTTC[A/G]CATTGGAAAACAAAG | 10451 |
rs75366703 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107880404 | TCTCTGGACAAGAGC[A/G]CTGACAGAAGGAACA | 10451 |
rs75382989 | snp | C/T | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107814313 | TCTCGCCAGCACCCA[C/T]TAGTTTTTGTCTTTT | 10451 |
rs75384963 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107616065 | CAAAGACTTAGAAAC[A/G]GAATTACCATTTGAC | 10451 |
rs75387390 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107622718 | TGTGGAGATTACTAA[C/G]CAATTTATCACACAT | 10451 |
rs75409167 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107826280 | ATTTGCTCCATTACG[C/T]TACTTGCTATGCAGA | 10451 |
rs75410341 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107807439 | CAGGACTTTTAGAGA[C/T]ACTCTTAAAAGATTT | 10451 |
rs75438160 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | VAV3 | GRCh38.p7 | 1:107644311 | TAATATAAAGTGGAA[A/T]AATTTTTTAAATGGA | 10451 |
rs75443442 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | VAV3 | GRCh38.p7 | 1:107703195 | AGAGATTAAAGAATG[C/G]GGCATATAAAGATGG | 10451 |
rs75446852 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | VAV3 | GRCh38.p7 | 1:107831219 | CTTTTAAATTGTTTT[C/T]ATAAACAATACATGA | 10451 |
rs75453797 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107827510 | GTGATTAACAATTGA[C/T]TGATACAAGGAGAGA | 10451 |
rs75458126 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107865390 | TCAGATTTTAAGCAG[C/T]GTGTGTATGAGTGTA | 10451 |
rs75474887 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107960475 | GTCTCAAAAAAAAAA[-/A]AGAAAAGAAAAGAAA | 10451 |
rs75483934 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107768649 | AAATTGTAGAAACTA[C/T]TTTCTCTAACTTAAA | 10451 |
rs75488558 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | VAV3 | GRCh38.p7 | 1:107640900 | ACTATAGAAAATGAG[C/T]CAGTGGAGAGAATGA | 10451 |
rs75497394 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689511 | TCTTTTCTCTCTAGC[C/T]TTTTTTTTTCTTTTT | 10451 |
rs75498479 | snp | A/G | 0 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570982 | CCTCCTACTAGACGC[A/G]TAGCGTCCACGGGGC | 10451 |
rs75518592 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107764118 | AAACAAAAAAAAAAA[A/C]ATGATGTACAAAAAA | 10451 |
rs75538008 | snp | A/G | 0.0984431 | 0.198823 | intron-variant | VAV3 | GRCh38.p7 | 1:107956645 | GAAATTGTAGGACCC[A/G]TAAAAGCACTTCAGG | 10451 |
rs75553023 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107671425 | TTTTCATGATGACAT[A/G]TAAGACTTGCCAAAT | 10451 |
rs75556576 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107796802 | TTGTAAAAAAAAAAA[A/T]AAATATATATATATA | 10451 |
rs75558841 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896829 | TGTATTAGAGGGGAA[A/C]TATGAAACATTTGCC | 10451 |
rs75566953 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | VAV3 | GRCh38.p7 | 1:107660496 | AATACGCACCAGGCC[A/G]AGGCAGACCACTGGC | 10451 |
rs75569843 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107879711 | CATACCTATTTTTGA[A/C]AAAAAAAAAAATTGT | 10451 |
rs75570391 | snp | A/G | 0.267636 | 0.249377 | intron-variant | VAV3 | GRCh38.p7 | 1:107813072 | AGCTGGCAGTGAGCC[A/G]AGATTGCGTGCACTC | 10451 |
rs75571401 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107854460 | AACAAAAAACAATTC[C/T]CTTGTTTTCCACAAA | 10451 |
rs75572883 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | VAV3 | GRCh38.p7 | 1:107611508 | TTCTGAAATGTGATG[C/T]GAAAAATATTTCCTC | 10451 |
rs75594729 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107790494 | AGAGGAATGGCACAC[A/C]GTGCCAGAGGAGAGG | 10451 |
rs75597571 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107856623 | ACTTTATTTTGTTCT[C/G]AAGTTTAATTCTCTT | 10451 |
rs75598209 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | VAV3 | GRCh38.p7 | 1:107831828 | ATTCTCATGTAACCA[C/T]AGTAAAAACCAGAAT | 10451 |
rs75598733 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107916961 | TGAGGGGATGTAAAG[C/T]GTGAAGGCAGTGACT | 10451 |
rs75600679 | snp | C/T | 0.110167 | 0.207236 | intron-variant | VAV3 | GRCh38.p7 | 1:107838717 | CCAAGTGCCCAACAA[C/T]GGTAGACCAGATAAG | 10451 |
rs75606004 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107653215 | ATGCAAATGACTCTG[C/T]ACCATCATTTCGATG | 10451 |
rs75614459 | snp | A/C | 0.175576 | 0.238665 | intron-variant | VAV3 | GRCh38.p7 | 1:107639904 | GTAGTACCACACACT[A/C]CAGCCTGGGCAACAG | 10451 |
rs75620692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107920043 | CATAATGTCTGACCT[C/T]ATCTCCTTATTACAG | 10451 |
rs75658005 | snp | A/G | 0.444444 | 0.157135 | intron-variant | VAV3 | GRCh38.p7 | 1:107913360 | TGATGATCCTCTGGC[A/G]TGCCATTGTGCCCAG | 10451 |
rs75664198 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107733169 | TATTCCTTTCTGTTT[A/G]TTAGTTTTCCTTCTA | 10451 |
rs75700031 | snp | C/T | 0.23031 | 0.249223 | intron-variant | VAV3 | GRCh38.p7 | 1:107814381 | CATTGTGGTTTTGAT[C/T]TGCATTTCCCGATGA | 10451 |
rs75709540 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107720471 | AAAAAAAAAAAAAAG[A/G]AGTTTGAGACCAGCC | 10451 |
rs75739737 | snp | A/C | 0.172351 | 0.237636 | intron-variant | VAV3 | GRCh38.p7 | 1:107671162 | TTCACGTCCTCTAGA[A/C]AAACTGAAAGAGTAA | 10451 |
rs75746646 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107662402 | CCTGAAAGGATTTCT[A/G]TAAGGGAAAAAAAAA | 10451 |
rs75750534 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | VAV3 | GRCh38.p7 | 1:107790228 | ATATCCTTCCACACA[A/G]GCCTTATGTGCTTCC | 10451 |
rs75758271 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107639388 | AAGAGAATAAAAAAA[-/AA]GCCACAGATTAGGAG | 10451 |
rs75772592 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107670090 | TTTCATCTCCATTTT[A/C]CAGATTAGAAAACTG | 10451 |
rs75778624 | snp | A/G | 0.227959 | 0.249026 | intron-variant | VAV3 | GRCh38.p7 | 1:107817168 | ACGCATTATGATAGT[A/G]GGCAGACAAAAAATT | 10451 |
rs75781995 | snp | C/T | 0.189261 | 0.242509 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592199 | TTTCTTTAATGACAC[C/T]GAAGGTTTTAGAGTA | 10451 |
rs75795166 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107926582 | ATGCCACCCCTCCCC[-/C]CATCTCCTGGTAGTA | 10451 |
rs75817904 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107805151 | AAAGCCTTATTGGGG[C/T]TGAATCTGTTTGCTG | 10451 |
rs75879444 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107685460 | GATTATTAGCTTTTT[A/G]TTATTTTAAATGTTT | 10451 |
rs75893236 | snp | A/C | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107704183 | GAAATTTAAGAACTA[A/C]AGATAGAAGAATATA | 10451 |
rs75908656 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107725468 | ATACTAAGCATTTAC[C/T]GGCTTTTGACCAAAC | 10451 |
rs75923647 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107624079 | TTGTGTTTATTACAT[C/T]TCTGAAATTTTGGCA | 10451 |
rs75924637 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107586141 | CTCCCTTGGCATAGT[A/T]TTTTTTTTTTTTTTT | 10451 |
rs75928078 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107949409 | TTGACCCTGCGGGCT[A/C]AAGAGATCCTTCCAC | 10451 |
rs75954076 | snp | C/T | 0.112631 | 0.208878 | intron-variant | VAV3 | GRCh38.p7 | 1:107957665 | ACTGAGAAGGAATAA[C/T]AAGAGGTACAAGAGA | 10451 |
rs75961762 | in-del | -/AG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107586138 | CCACTCCCTTGGCAT[-/AG]TTTTTTTTTTTTTTT | 10451 |
rs75978967 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794669 | AAAATCCTAAAAGGA[A/G]TTTCCACCTTAGGAG | 10451 |
rs75984967 | snp | C/G | 0.5 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107571000 | GCGTCCACGGGGCTG[C/G]CGGGCGGGGGGGTGG | 10451 |
rs75993514 | snp | C/T | 0.179105 | 0.239737 | intron-variant | VAV3 | GRCh38.p7 | 1:107625690 | TTGATTTGTTAGAAA[C/T]TGCATTCATTGATTC | 10451 |
rs76007771 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107911278 | ACATGTATATATCTG[C/T]GTATTGTATTCCTTT | 10451 |
rs76013032 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | VAV3 | GRCh38.p7 | 1:107879204 | TAGCTCTGGAATCAG[C/T]CATTTCTCCAAATAA | 10451 |
rs76031374 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107879627 | AATCATCTGAAGCAG[C/T]TTCAAATATACTGCC | 10451 |
rs76032089 | snp | A/G | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570926 | ACCTGCGGCGGCTCT[A/G]CCCGGGCCCAGCCCT | 10451 |
rs76036239 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107923654 | GGGTCTAGCATTTCC[A/C]GTTTGCACTTCTGTC | 10451 |
rs76046087 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107903417 | AATGTGACCTCTGAG[G/T]GTACAAGCAGAAAGT | 10451 |
rs76050750 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107836056 | TTTTTAGAGACCCAC[A/G]AAAAGACAGGCACAA | 10451 |
rs76052646 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107674487 | AACTCTGAAAATCAG[A/C]CCAGATCCCACTGCT | 10451 |
rs76053420 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | VAV3 | GRCh38.p7 | 1:107836185 | ACAAATTGGACCTAA[C/T]AGACATTGACAGAAT | 10451 |
rs76071182 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | VAV3 | GRCh38.p7 | 1:107943911 | TCCAAGCTGTGCCCA[C/T]AAAACCCAAAAAGCC | 10451 |
rs76073012 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107658132 | ATAAAGTACGTTCAA[C/T]GTGAAACACACAATA | 10451 |
rs76104225 | snp | A/C | 0.040671 | 0.13668 | intron-variant | VAV3 | GRCh38.p7 | 1:107843106 | GCTGTTCCAATTTAT[A/C]GTGAAACCTATGAGT | 10451 |
rs76118396 | snp | C/T | 0.17654 | 0.238964 | intron-variant | VAV3 | GRCh38.p7 | 1:107638003 | GCATTTGAGAAAAAT[C/T]TGACATCTATTACTG | 10451 |
rs76119888 | snp | G/T | 0.0566069 | 0.158427 | intron-variant | VAV3 | GRCh38.p7 | 1:107759996 | TAAGGAATAATCAGG[G/T]TTTGAATTTTTCTGA | 10451 |
rs76121422 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107918214 | TTGGGAAAGATAGCA[C/T]AGTAAGAAAGGGACA | 10451 |
rs76125233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888139 | CTTACTGGCATAATA[A/G]AATACATCAGAGAAC | 10451 |
rs76134821 | snp | A/G | 0.228547 | 0.249078 | intron-variant | VAV3 | GRCh38.p7 | 1:107815121 | GCTGCAGTATCTGTC[A/G]TTCACTTCGGCTGCT | 10451 |
rs76152602 | snp | C/T | 0.0919752 | 0.193722 | intron-variant | VAV3 | GRCh38.p7 | 1:107938575 | ATTAGGATGTCAGAA[C/T]AATCCAGAAGTGCCC | 10451 |
rs76181431 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107817870 | TCAGAGCGGAAAAAA[A/T]TGCAATTTACTGCTC | 10451 |
rs76186008 | snp | A/G | 0.498754 | 0.0249289 | intron-variant | VAV3 | GRCh38.p7 | 1:107701342 | ACCCTCTGAAGCAAC[A/G]GCCTGAGCTGTACGT | 10451 |
rs76196430 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | VAV3 | GRCh38.p7 | 1:107794958 | AGCATTGTTCTCTGA[C/T]GGTTTTTCATTGTTA | 10451 |
rs76200214 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | VAV3 | GRCh38.p7 | 1:107822264 | TGCCCTGTAGGGAAT[C/G]TATGGTGAAGGGAAG | 10451 |
rs76231380 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858286 | CATATTGACAGCACT[C/G]AAATTATACAAGATT | 10451 |
rs76247618 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | VAV3 | GRCh38.p7 | 1:107809385 | CCAGAAAGAAAAGAG[A/C]ATTACTGTATCAGCA | 10451 |
rs76254117 | snp | A/G | 0 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570991 | AGACGCATAGCGTCC[A/G]CGGGGCTGGCGGGCG | 10451 |
rs76254422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624788 | AGTAGTGCTTTAAAG[A/G]AAAGTTTATTGACTT | 10451 |
rs76257606 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107808055 | ATTTTGGAATCCAAA[C/T]TCTTGCATAGAAACG | 10451 |
rs76261229 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107959033 | TCGGGAGGCCAAGGC[A/G]GCCTGATGACCTGAG | 10451 |
rs76264876 | snp | G/T | 0.277778 | 0.248452 | intron-variant | VAV3 | GRCh38.p7 | 1:107741527 | ACATGCATGACATAA[G/T]CCCCACTGTGACGCC | 10451 |
rs76267615 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963658 | CTGGTTGCTAAGTAG[C/T]TGAGGCTCTGCGTCA | 10451 |
rs76298220 | snp | C/T | 0.0788843 | 0.182262 | intron-variant | VAV3 | GRCh38.p7 | 1:107802636 | TAGGTAAAGAGGATA[C/T]ATTACATTTATTAAT | 10451 |
rs76302796 | snp | C/T | 0.115438 | 0.210697 | intron-variant | VAV3 | GRCh38.p7 | 1:107831759 | CTCCCAGCATCATGC[C/T]AGTATATAATAGACT | 10451 |
rs76312644 | snp | C/T | 0.111224 | 0.207945 | intron-variant | VAV3 | GRCh38.p7 | 1:107930314 | GTATACCTATGTACC[C/T]ACAAAAATTAAAACT | 10451 |
rs76327812 | snp | C/T | 0.212728 | 0.247206 | intron-variant | VAV3 | GRCh38.p7 | 1:107952672 | TCACTCTAACCCAAA[C/T]GGCTCCCTTCCCATC | 10451 |
rs76345198 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107761459 | AAAATCATGGCCCCC[A/C]AGGGTCTTCTTCAGT | 10451 |
rs76357498 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107947105 | TAACCTTTTTGCTAT[A/G]AAATGCCACCCACTG | 10451 |
rs76359608 | snp | A/G | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107803932 | GTGCTTTAGTGTTGG[A/G]TGCATATTTATAATT | 10451 |
rs76369741 | snp | C/T | 0.0437281 | 0.141251 | intron-variant | VAV3 | GRCh38.p7 | 1:107721249 | GGGAGCATATGTCCA[C/T]TCAGCAGAATAATTA | 10451 |
rs76374437 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | VAV3 | GRCh38.p7 | 1:107861516 | TATAGATATAAGGAG[C/T]AGATGCATAGCTAAT | 10451 |
rs76376650 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107823554 | CTCCAAATTTTAGAG[A/G]TCAAGCAGTGGAAGA | 10451 |
rs76379499 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107802333 | TTCCTTTCCAATATG[G/T]ATGGCCTTTATTTCT | 10451 |
rs76408496 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858283 | TAACATATTGACAGC[A/C]CTGAAATTATACAAG | 10451 |
rs76409831 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107708209 | GGAAGAAAAAAAAAA[G/T]TTCTGCTGCTACTAC | 10451 |
rs76410394 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107863385 | CTACAGCCTCCCCCA[C/G]TGACAGAATGCTTAG | 10451 |
rs76410468 | snp | C/T | 0.046775 | 0.145601 | intron-variant | VAV3 | GRCh38.p7 | 1:107815895 | GGTGTGGAGGGGGCA[C/T]GGGGGGATGGTTTCA | 10451 |
rs76413318 | snp | C/T | 0.00752541 | 0.0608775 | intron-variant | VAV3 | GRCh38.p7 | 1:107757352 | GAAGATATGGTTTAG[C/T]ACTACTTTCATCAAA | 10451 |
rs76414015 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107731551 | TTAGGAAATTATACT[C/T]TAACAGACAAAGAAT | 10451 |
rs76415197 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107887626 | AGAAAGTTTTTAAAA[A/C]TCTTTTACAATGCAT | 10451 |
rs76419057 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107935097 | TCAGCCAATTTGCCA[A/G]TGAGAACAATTGGCA | 10451 |
rs76424058 | snp | A/C | 0.030278 | 0.119257 | intron-variant | VAV3 | GRCh38.p7 | 1:107890494 | CTTGCTAATCCAAAC[A/C]ATCTCTATTACCCCT | 10451 |
rs76445487 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107906796 | TGAAAAAGGGAGAAA[A/T]GCAGGGTGAGAAGGA | 10451 |
rs76445664 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107801221 | TACTATATTTTTGTA[C/G]TATATTTGGAAGTCA | 10451 |
rs76447272 | snp | A/G | 0.0287284 | 0.116357 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591435 | AATGAATGAATGAAT[A/G]AATGAATGAATGAAT | 10451 |
rs76465329 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107672533 | CAGTAAAACAGATCA[G/T]AAATAAAATGTCTGT | 10451 |
rs76474620 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107813119 | GCCAGACTCCGTCTC[A/C]AAAAAAAAAAAAAAC | 10451 |
rs76497323 | snp | C/G | 0.110167 | 0.207236 | intron-variant | VAV3 | GRCh38.p7 | 1:107914446 | ATGTGATTTATAGGT[C/G]AATTATTTGAGTCCT | 10451 |
rs76498889 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107704189 | TAAGAACTAAAGATA[A/G]AAGAATATATTCTTT | 10451 |
rs76502026 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107608255 | CCTGAATGGTTCTTA[A/G]GTACCTAATAAGTTT | 10451 |
rs76504820 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107740620 | TAAAAGAAAAAAAAA[A/T]TCACACTTCTACAAA | 10451 |
rs76508730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107610128 | AATCATAGTATCTGT[C/T]AGATAAGTAGAAAAT | 10451 |
rs76533505 | snp | C/T | 0.111224 | 0.207945 | intron-variant | VAV3 | GRCh38.p7 | 1:107930700 | TAATAAATGACATGA[C/T]TGATGAAAAGTCAAT | 10451 |
rs76540593 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107839151 | TAGTAGTCAAATGCA[C/T]AAGTTAGCATTTCTT | 10451 |
rs76543525 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107911483 | GATAAATTTTGAATG[C/T]GTTATATAGCAGGGT | 10451 |
rs76547624 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107922347 | AGGCAGTAGAAGGGA[A/T]TTTTAGGCATATTTT | 10451 |
rs76552397 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107920713 | AAGAAAATACAAACA[C/T]TTCCTTCTCCTCCAG | 10451 |
rs76554699 | snp | C/T | 0.0980852 | 0.198549 | intron-variant | VAV3 | GRCh38.p7 | 1:107958389 | AACAATGTATGGTTG[C/T]GTACAGCAGAAACTA | 10451 |
rs76559818 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107862703 | AAGCCAATGTGACAA[G/T]GTCAAGGATTTCTGA | 10451 |
rs76568279 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107807112 | TTCAGTACAGAAGGA[C/T]GACTGTACATTAAAG | 10451 |
rs76590353 | snp | A/T | 0.276267 | 0.248616 | intron-variant | VAV3 | GRCh38.p7 | 1:107800002 | TCTCCAGTCCCATCC[A/T]TGTTGCAACAAATGA | 10451 |
rs76590727 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107841393 | AAAGGGCACAGAAAT[A/T]GTCAGAAGGCTGAGG | 10451 |
rs76599701 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107698517 | AGTTTTGACTTACGA[C/T]AGTTTCCACTTACAA | 10451 |
rs76606555 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107674987 | CAGTCCAAAAGGAAT[C/G]GAATCCCGCGAAAAG | 10451 |
rs76612125 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107816311 | GCCTATTTTCTCATA[C/T]AAAGTGATAAAATAA | 10451 |
rs76614519 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107851966 | AATTCTCAATTTCAA[A/G]TACAATACAGTGAGA | 10451 |
rs76614740 | snp | A/G | 0.110519 | 0.207473 | intron-variant | VAV3 | GRCh38.p7 | 1:107924755 | AGACACCATTGGGGG[A/G]AAAAAAACTGTGACC | 10451 |
rs76615146 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107773681 | ACTTTGGGACACCAG[A/G]GAGATGGTGATCCAT | 10451 |
rs76617369 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107805568 | GAATTGCTTTTCTGT[A/G]TTATCTTGGAGATGA | 10451 |
rs76618155 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107924021 | CCTACAGTATTTTGT[A/T]ATAGCAGCCCAAATC | 10451 |
rs76670042 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907205 | AATTTTCCCTGAAGA[A/C]TAAATGGTCATATAC | 10451 |
rs76672199 | snp | A/G | 0.108755 | 0.206276 | intron-variant | VAV3 | GRCh38.p7 | 1:107912083 | TGTGTGCGTGTTTAC[A/G]TTAGTTTCCTATGAA | 10451 |
rs76676166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107630195 | CCTATCCTGAGTTCT[A/G]ATCATTCCTTACATC | 10451 |
rs76690918 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107879712 | ATACCTATTTTTGAC[A/C]AAAAAAAAAATTGTA | 10451 |
rs76698933 | snp | A/G | 0.298144 | 0.245321 | intron-variant | VAV3 | GRCh38.p7 | 1:107835331 | GGTGCCAAGCAGCTA[A/G]AGGACAAAGCCTCAG | 10451 |
rs76699514 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107880813 | AAAAAAAAAAAGAAA[A/G]GAAAAAAAGCACCAA | 10451 |
rs76712423 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107640531 | CAAAAACTTTTAGGG[A/C]TGATATTGGATATGT | 10451 |
rs76718848 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107902069 | ACAAAAAAAACAACA[A/C]CAAAAACTGTTATTG | 10451 |
rs76740751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107763360 | GGCAAAACTTTGACA[A/G]TAACTCTGAAAGAAG | 10451 |
rs76740967 | snp | C/T | 0.177503 | 0.239258 | intron-variant | VAV3 | GRCh38.p7 | 1:107677407 | CCTCTCAGAGGTTGC[C/T]GGCCCATAAGAAATT | 10451 |
rs76741490 | snp | G/T | 0.0685596 | 0.171987 | intron-variant | VAV3 | GRCh38.p7 | 1:107824996 | TCTCTAAACTAAAAG[G/T]CAGTAAACTACCACA | 10451 |
rs76742805 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107813633 | AGTCCTCTCTTCTAG[C/T]TATTTTGAAAAATGT | 10451 |
rs76762105 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107858583 | ATTCTCATAGAAGCA[C/T]GAAGCCTACTGTGAA | 10451 |
rs76762654 | snp | C/T | 0.109461 | 0.206758 | intron-variant | VAV3 | GRCh38.p7 | 1:107958018 | TTAAGCCACCAATCA[C/T]GCAGACAGAACAAGT | 10451 |
rs76766761 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107928666 | TTTAAGCAGAATTAG[C/T]GAGCTTGACAGCAGG | 10451 |
rs76779493 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107784324 | CATATGTATACATCT[A/G]CTTTATTCATTTTAG | 10451 |
rs76803060 | snp | C/T | 0.283421 | 0.247756 | intron-variant | VAV3 | GRCh38.p7 | 1:107728630 | ATATGTATATGTATA[C/T]GTATATGTATATGTA | 10451 |
rs76804309 | snp | C/T | 0.319616 | 0.240112 | intron-variant | VAV3 | GRCh38.p7 | 1:107804132 | GCCTACATGTGTCTT[C/T]ATAGGTGAGGTGGGT | 10451 |
rs76812741 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107856122 | GGAGTGGGTGAGAAG[C/T]AAGATGAGAGAAAAG | 10451 |
rs76829753 | snp | C/T | 0.030665 | 0.119967 | intron-variant | VAV3 | GRCh38.p7 | 1:107657598 | CAGTGGTTCATATCA[C/T]TTTGGACGTATTACT | 10451 |
rs76853802 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107930147 | TGACTGTAGTAAAAA[-/A]ATAATTGTACATTTA | 10451 |
rs76874135 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107940655 | TTAGCCTTAGAAAGG[A/G]AAGAAATTCTGGCAC | 10451 |
rs76882803 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107611067 | CTGCAATCCTTGGGA[C/G]TAGAGATGTTTCACA | 10451 |
rs76894643 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107790047 | AGAAGACTCCACAGA[A/C]GCAGGTGGTAGCATA | 10451 |
rs76921795 | snp | A/G | 0.113685 | 0.209567 | intron-variant | VAV3 | GRCh38.p7 | 1:107840872 | ACTATAAACCACTGG[A/G]AGGAAGTGAAAACTC | 10451 |
rs76952448 | in-del | -/A | 0.0607341 | 0.163335 | intron-variant | VAV3 | GRCh38.p7 | 1:107841846 | AGAAAATATCTCATT[-/A]ATACTTTGTGTATTG | 10451 |
rs76964864 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | VAV3 | GRCh38.p7 | 1:107813883 | TGTGCCTGAGTTATT[A/G]CACTTAACATAATGA | 10451 |
rs76965144 | snp | A/T | 0.322007 | 0.239405 | intron-variant | VAV3 | GRCh38.p7 | 1:107807554 | CCAGGGCCACTGCAC[A/T]TGGCCTTGTGCAATG | 10451 |
rs76968958 | snp | A/C | 0.118933 | 0.212888 | intron-variant | VAV3 | GRCh38.p7 | 1:107920312 | GATAAAATGCATAGG[A/C]GTTCATCATTACCAC | 10451 |
rs77012289 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107760039 | ACAAAAATAGAGATG[A/C]CTAATAATTTTGCAG | 10451 |
rs77015626 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107681670 | TTTTTTTTTTTTTTT[G/T]TTGAGACAGAGTCTC | 10451 |
rs77031967 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107946189 | GAGACTAATTAGGAG[C/G]CAGTGGTCCAAGTGA | 10451 |
rs77047250 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107868934 | TTGGGCACAGCACTG[A/T]TTCCCACTTCACAGG | 10451 |
rs77067430 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | VAV3 | GRCh38.p7 | 1:107861206 | GCTTATCTTTCTACA[A/C]GTCTATGTATTTGGA | 10451 |
rs77068826 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107930335 | AATTAAAACTAAAAA[A/C]TTTTTTTAAAGAATT | 10451 |
rs77073618 | snp | A/C | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570936 | GCTCTGCCCGGGCCC[A/C]GCCCTGGGCTTCAAG | 10451 |
rs77076921 | snp | C/G/T | 2.28048e-05 | 0.00337666 | intron-variant | VAV3 | GRCh38.p7 | 1:107705071 | TTAGACCTAAAAAAA[C/G/T]GAAAAAAATAACTTT | 10451 |
rs77084557 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689755 | TTCTTCTTTTCCTCC[C/T]TATTGGAAACACATA | 10451 |
rs77085008 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | VAV3 | GRCh38.p7 | 1:107815317 | GACTAACTTGGGAGT[C/T]AGTGAGGGGAAAGGG | 10451 |
rs77086949 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | VAV3 | GRCh38.p7 | 1:107630920 | GAGTAAGTACAGATT[C/T]AACCCAGTTTCCTAC | 10451 |
rs77088232 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107936809 | CCTTTCCTGGTTGGA[A/C]TTTATGCACTTATGC | 10451 |
rs77089132 | snp | A/G | 0.277778 | 0.248452 | intron-variant | VAV3 | GRCh38.p7 | 1:107701119 | TGGACAAAGGACATG[A/G]ACAGACACTTCTCAA | 10451 |
rs77097831 | snp | A/G | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107808857 | TAATACTGCTGTATC[A/G]AAATATTTATCCATA | 10451 |
rs77125988 | snp | A/C | 0.229136 | 0.249128 | intron-variant | VAV3 | GRCh38.p7 | 1:107822089 | GCAGGACTAGGGCAA[A/C]AACTCACCAGGTGGG | 10451 |
rs77127620 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107626115 | TTGCACTGTACCAAG[C/T]ATTGGAAAAATACAA | 10451 |
rs77131399 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107770382 | ATTCTAATCCTCCCA[C/T]GGGAAAAAGTGTCAT | 10451 |
rs77149713 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107902633 | TATTTTAGAATAACC[G/T]GAGGTCCTACATGTT | 10451 |
rs77152677 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107729714 | TGAGCATCCAAAGCA[C/T]AGCATTGTGCTTGGA | 10451 |
rs77191572 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107922306 | TTGTGTCAGTATCCA[A/G]AAAAAAAAAATCACT | 10451 |
rs77197538 | snp | A/G | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570763 | TTGGCTGAGGGCAAC[A/G]GAGGCCATCGCCTGT | 10451 |
rs77206990 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107800234 | AAGTGCTAGGTTATA[A/T]AATAATTCAATATTT | 10451 |
rs77209892 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107957895 | TTAAAAAAAAAAAAA[A/G]ACACGATCTCATTTC | 10451 |
rs77223533 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107853860 | AAGAATATTCCACAG[A/C]CAACTTATTTATGAG | 10451 |
rs77236984 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107740727 | ATCTTATTTGTGCTG[C/T]AGGACAGGGGTCACT | 10451 |
rs77241154 | snp | C/T | 0.0487381 | 0.148303 | intron-variant | VAV3 | GRCh38.p7 | 1:107808678 | TATAATCTGAAGTGT[C/T]GCCCCAATGATTCAG | 10451 |
rs77250605 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107914175 | ACAGACAGATGAATG[C/T]AAATGGCTAATGAGT | 10451 |
rs77256294 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947401 | AGTTCTAAGAGTTCC[A/C]AAAGAACTGTGAGGA | 10451 |
rs77293732 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922295 | AATGTCTTGTTTTGT[C/G]TCAGTATCCAGAAAA | 10451 |
rs77293837 | snp | C/G | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570734 | TTCGGGATCTGAACC[C/G]GACTCCCTTTCGATT | 10451 |
rs77309466 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107902245 | GACTTTGCCTAGTTT[C/T]CTGTGCTAAGTTTCT | 10451 |
rs77329106 | snp | A/G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570952 | GCCCTGGGCTTCAAG[A/G/T]CTCACCGCAGCGGCC | 10451 |
rs77330684 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107802634 | GTTAGGTAAAGAGGA[C/T]ACATTACATTTATTA | 10451 |
rs77335801 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | VAV3 | GRCh38.p7 | 1:107750140 | TAGATAATTTGCTCA[A/G]GATCACACTGCTAGT | 10451 |
rs77346255 | snp | C/G | 0.230603 | 0.249246 | intron-variant | VAV3 | GRCh38.p7 | 1:107833382 | AACTGTAGAAGAAAA[C/G]TTTGAAGCTAACAGA | 10451 |
rs77352406 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107623592 | GGCAGTACACATATT[A/C]TTTCATTGTTAATTG | 10451 |
rs77365194 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | VAV3 | GRCh38.p7 | 1:107958983 | AACTATATCTAGGCC[A/G]GGCACAGTGGCTTAC | 10451 |
rs77375597 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107917325 | TCACCACATACCAGG[C/G]ACCACGCTAAGCACT | 10451 |
rs77393006 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107698277 | ATATTTGAATTTTGA[C/T]ATTTTCCCGGGCGAG | 10451 |
rs77405871 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107791549 | CAGATGGCAGAGACC[C/G]TGGCTGAATGTTAGA | 10451 |
rs77435676 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107842826 | ATTTCTCCCGATTTT[A/T]ATAACCATAGCTAAG | 10451 |
rs77436595 | snp | A/C | 0.0792508 | 0.182605 | intron-variant | VAV3 | GRCh38.p7 | 1:107852918 | CACCAACATTTCACA[A/C]CACCTTTATCAATTC | 10451 |
rs77436627 | snp | A/T | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107815486 | TTTACGCACTGTTCC[A/T]GGCTGCCTGGTTCTA | 10451 |
rs77440703 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107645337 | TTTTTTTTTTTTTTG[G/T]TCATTTGTTAGGGTT | 10451 |
rs77454105 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | VAV3 | GRCh38.p7 | 1:107752794 | TTACCCAAACAAACC[A/G]AATAGTGAGTGTTGG | 10451 |
rs77454414 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | VAV3 | GRCh38.p7 | 1:107751742 | TAGGACCTCAAGGAC[A/G]AAAAGCTCTGAGTTA | 10451 |
rs77455034 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107708330 | CAGATTAGTTAACTC[A/G]CTCAGTCATGCTGAT | 10451 |
rs77462017 | snp | C/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107615554 | GCAAAGATTTAATGA[C/G]TAAGATGCCAAAAGC | 10451 |
rs77469433 | snp | A/G | 0.110872 | 0.20771 | intron-variant | VAV3 | GRCh38.p7 | 1:107839923 | CAAATTTGATAACTT[A/G]GGTGAAACAGGCCAA | 10451 |
rs77475507 | snp | A/C | 0.237593 | 0.249692 | intron-variant | VAV3 | GRCh38.p7 | 1:107819485 | CAAGACCAGCCTGCA[A/C]AACATAACAAGACTC | 10451 |
rs77477575 | snp | A/G | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107806170 | TGTGCTGCTTCCTAT[A/G]GGTTTAGGCAGGGCA | 10451 |
rs77483647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107874285 | ACATGTGTTTAGTGT[A/G]CATACGGATAACAGT | 10451 |
rs77490458 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107728017 | TAGAAAGTTTCATGC[G/T]AGTATCAAGTATTCA | 10451 |
rs77503483 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107670089 | TTTTCATCTCCATTT[A/T]ACAGATTAGAAAACT | 10451 |
rs77504590 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107868115 | GCACCACACTAGCAG[A/G]CAGAGAGATCAAGCT | 10451 |
rs77512682 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107760038 | AACAAAAATAGAGAT[C/G]ACTAATAATTTTGCA | 10451 |
rs77524943 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107916397 | TAACGTACAAATCTG[A/G]TTTCAAATATATTGC | 10451 |
rs77557623 | snp | C/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107665953 | AAGGAAGGTAGAATT[C/G]TGAGGAAAAAGGAAA | 10451 |
rs77585246 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | VAV3 | GRCh38.p7 | 1:107751706 | ATTTGGTCTATAAAG[C/T]CCAGGCTGGCTTTCT | 10451 |
rs77591951 | snp | A/T | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107814135 | GCAGGTATTCCTTTG[A/T]TATACTTTTTTTCTT | 10451 |
rs77607193 | snp | A/C | 0.148326 | 0.228391 | intron-variant | VAV3 | GRCh38.p7 | 1:107855613 | TAAATTTGTTAAGAG[A/C]AGGGGCAGGAATTGT | 10451 |
rs77612441 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107949921 | AACTTTTTCTATCAG[A/G]TATTGCCTATATGAT | 10451 |
rs77646655 | snp | G/T | 0.0970103 | 0.197722 | intron-variant | VAV3 | GRCh38.p7 | 1:107824921 | GTAAAAGAACCCACA[G/T]ATGCTGAAGAAGGTA | 10451 |
rs77648134 | snp | C/T | 0.226188 | 0.248863 | intron-variant | VAV3 | GRCh38.p7 | 1:107929546 | GAATATTATATAACA[C/T]TGTAACTATAGTAAG | 10451 |
rs77684469 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591427 | GATGAATGAATGAAT[A/G]AATGAATAAATGAAT | 10451 |
rs77692340 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107740186 | CAGCTACTCAGGAGG[A/C]TGAGGCAGGAGAATC | 10451 |
rs77693068 | snp | G/T | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107798218 | ATTTTTGAATATTTA[G/T]TCTAATTTCAACATC | 10451 |
rs77705025 | snp | C/G | 0.295343 | 0.245854 | intron-variant | VAV3 | GRCh38.p7 | 1:107836350 | AACAACAAAATGAAG[C/G]TGGAAATCAAAAAAT | 10451 |
rs77733364 | snp | A/G | 0.116488 | 0.211364 | intron-variant | VAV3 | GRCh38.p7 | 1:107910930 | AGTTGCAGTGGGCCG[A/G]TATCACACCATTGCA | 10451 |
rs77735683 | snp | A/G | 0.0588605 | 0.161139 | intron-variant | VAV3 | GRCh38.p7 | 1:107633797 | CCATGCTGTGAGGAA[A/G]ATAAGGAACCACTGA | 10451 |
rs77770863 | in-del | -/A | 0.0209421 | 0.100162 | intron-variant | VAV3 | GRCh38.p7 | 1:107835716 | AGCTGTCTGCAGGGC[-/A]AAAAAACCCCGGCCC | 10451 |
rs77785262 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107677421 | CTGGCCCATAAGAAA[C/T]TACTGACTTTTCTTT | 10451 |
rs77799913 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107800034 | GATGTCATTCTTTTT[A/G]TGGCTGAATAATTGT | 10451 |
rs77801503 | snp | G/T | 0.0379877 | 0.132479 | intron-variant | VAV3 | GRCh38.p7 | 1:107806112 | CCCTGCCTCTGCCTT[G/T]TGTCTCCAGTTGTCC | 10451 |
rs77813752 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107697819 | ATTCAAACCTAAAAA[A/C]ACTGGGTAGTTACTA | 10451 |
rs77814095 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107907334 | TCCAACAACAGAATT[A/C]TAAAGAGCCATTCAA | 10451 |
rs77819196 | snp | C/G | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107808514 | TAGTATAAAAACTAA[C/G]AAATGATCTATTATT | 10451 |
rs77820600 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | VAV3 | GRCh38.p7 | 1:107959881 | ACACCATACTTCCTC[C/T]AGTCCTCTCCATTTC | 10451 |
rs77824687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875434 | GAAGAGGATGGTGGA[A/G]CAGAGATCTGAGGTG | 10451 |
rs77838328 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | VAV3 | GRCh38.p7 | 1:107863952 | TCTCTCTCCAGAAGT[A/G]TATGTACAGTCAAGT | 10451 |
rs77840457 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107938558 | TGCAGCCTAGGGACA[C/T]AATTAGGATGTCAGA | 10451 |
rs77841908 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | VAV3 | GRCh38.p7 | 1:107713714 | AACCAATGTCTTCAA[C/T]GACATCCTTATAAAT | 10451 |
rs77842965 | snp | C/T | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570776 | ACAGAGGCCATCGCC[C/T]GTCCATTCAGAATGG | 10451 |
rs77847185 | snp | A/G | 0.0744748 | 0.178019 | intron-variant | VAV3 | GRCh38.p7 | 1:107827201 | TCTGTGACTAAGCCA[A/G]ACAGAGGTAACATGA | 10451 |
rs77860261 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907204 | GAATTTTCCCTGAAG[A/T]ATAAATGGTCATATA | 10451 |
rs77873213 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107790680 | CCTTAAATGTCTTCC[C/T]TTTTTTTTTTTTTTT | 10451 |
rs77874422 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107954551 | TTTTTTTTTTTTTTT[G/T]TTGAGATGAAGTCTT | 10451 |
rs77915194 | snp | C/T | 0.111928 | 0.208413 | intron-variant | VAV3 | GRCh38.p7 | 1:107925925 | TACATATATAACATA[C/T]GTATATATAAACAGA | 10451 |
rs77957333 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858287 | ATATTGACAGCACTG[A/C]AATTATACAAGATTT | 10451 |
rs77959238 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107763681 | CAGTCTTAAAGTCAA[C/T]ATAATGAAGGAATAT | 10451 |
rs77965575 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107908397 | CAAAGTAAGATCGGT[G/T]ATTACCAATCTTCCT | 10451 |
rs77980438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841758 | CTTTAGACACTTGAA[A/G]TGAGGCTAGTCTAAA | 10451 |
rs78007896 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107874609 | ACCAGCAGAAAAAAA[A/T]TTATCTCTGGAGAAA | 10451 |
rs78020119 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107753531 | ATATATATATACGTA[C/T]ATATATATATATATA | 10451 |
rs78020265 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107666588 | TTTTTTTTTTTTTTT[G/T]GAGACGGAGTCTCAC | 10451 |
rs78023984 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107905872 | TGTAATAATCAAAAA[A/C]CTAACAAATAAATTC | 10451 |
rs78030018 | snp | G/T | 0.0562307 | 0.157967 | intron-variant | VAV3 | GRCh38.p7 | 1:107765473 | TTGAGTAGACATAAA[G/T]GCATTCCAAAAACAA | 10451 |
rs78046594 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107617649 | TAAGGAAAAAAAAAA[-/AA]TGCCAGTGTTGAGAA | 10451 |
rs78052577 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | VAV3 | GRCh38.p7 | 1:107843757 | TAAAATCAGACACGG[A/G]AAAATGCATTTTTGG | 10451 |
rs78066433 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107574657 | AACACTCAAAACAAC[A/G]AAATATTTTGCTCTG | 10451 |
rs78067330 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107764074 | TCGAACTCCTCTTCA[A/G]GAAAAAAAAAAACAA | 10451 |
rs78068305 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107670017 | GGCTAGGTTCAGTTT[C/T]CTATCTTGATTAATA | 10451 |
rs78071854 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107855786 | CAGCCAGGGGGAATA[A/C]AAGAGGACTCAAAGG | 10451 |
rs78081220 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786352 | CTGGGCTGATTAGAA[G/T]TGCAGGCTCAGAAGT | 10451 |
rs78081346 | snp | G/T | 0.108402 | 0.206034 | intron-variant | VAV3 | GRCh38.p7 | 1:107936031 | AAACTTTACTGAAAT[G/T]TTATGATTTGGGGAG | 10451 |
rs78081457 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107904648 | CTTCATTCATGCACA[C/T]CTTTATTCATTCAGC | 10451 |
rs78088580 | snp | A/G | 0.321053 | 0.23969 | intron-variant | VAV3 | GRCh38.p7 | 1:107807764 | ACCTTGAAATTCAAT[A/G]TAACTTATGGCATGT | 10451 |
rs78092533 | in-del | -/TGT | 0.433236 | 0.170072 | intron-variant | VAV3 | GRCh38.p7 | 1:107750013 | GAATGCCTTGAGAAG[-/TGT]TGTTCATCCCTTTCA | 10451 |
rs78094869 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | VAV3 | GRCh38.p7 | 1:107862323 | AAATGAGAGCATTCA[G/T]CCAGTTCCACCCCCA | 10451 |
rs78107633 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107808459 | TAATATTTCTGTTGG[A/T]ATATATTTTTTCAAG | 10451 |
rs78134093 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895916 | ATTACCCCTGAAACA[A/G]TTCAGCAGTAACACC | 10451 |
rs78134314 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | VAV3 | GRCh38.p7 | 1:107709316 | CATAGCTGATAGAAA[A/T]CAGAAAAAATATGCT | 10451 |
rs78136458 | snp | A/G | 0.228547 | 0.249078 | intron-variant | VAV3 | GRCh38.p7 | 1:107934886 | CAAATGAGAGGAGAC[A/G]TGCTACAAGAAACAA | 10451 |
rs78175580 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107805016 | ATGTATGTTTTCTGT[C/T]GAGAAGTCTGTTGCC | 10451 |
rs78182911 | snp | A/C | 0.0752113 | 0.178743 | intron-variant | VAV3 | GRCh38.p7 | 1:107707345 | ACATCCTAACTTGCA[A/C]ATCAGTAGCAGCGTG | 10451 |
rs78199812 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107960595 | ACAAGTCCTAAAAAT[C/T]GAGCTTCCATTTTCT | 10451 |
rs78223403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107926654 | AAGAGTGCAGCAAGC[A/G]CGAGGCATTGCATTT | 10451 |
rs78223483 | in-del | -/G | 0.326157 | 0.238118 | intron-variant | VAV3 | GRCh38.p7 | 1:107808679 | ATAATCTGAAGTGTT[-/G]CCCCAATGATTCAGA | 10451 |
rs78237463 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107879145 | TTGTTTCATTGCTTT[C/T]TTATATCAAGTTGTC | 10451 |
rs78239640 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733181 | TGATGTTGATGTTAT[C/T]CCTTTCTGTTTGTTA | 10451 |
rs78264169 | snp | A/G | 0.246769 | 0.249979 | intron-variant | VAV3 | GRCh38.p7 | 1:107703098 | TTACATTCTTCACAG[A/G]TATCATCTCATCAAG | 10451 |
rs78269015 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107789432 | TCCCAGCCTCAGGAC[G/T]GCTCAAAGAAAATCA | 10451 |
rs78276319 | snp | A/C | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107596237 | TGCTCTATTACCCCT[A/C]TGTCCAGCTGAATGT | 10451 |
rs78279722 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107708208 | AGGAAGAAAAAAAAA[A/G]GTTCTGCTGCTACTA | 10451 |
rs78285516 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107856081 | ACACTCATAAGCAAG[C/T]TCACAAATGACACTG | 10451 |
rs78287223 | snp | A/G | 0.226188 | 0.248863 | intron-variant | VAV3 | GRCh38.p7 | 1:107780024 | AAAGTTCTATTGGAC[A/G]GTCCTGCTATATAGC | 10451 |
rs78288249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107722751 | GTTTCATCCTTTAAG[A/G]TACCTTGGGCTTCTT | 10451 |
rs78288858 | snp | A/T | 0.209084 | 0.246629 | intron-variant | VAV3 | GRCh38.p7 | 1:107819671 | AATTCGATTGGGGGA[A/T]TTTATGTAGGATTTC | 10451 |
rs78321041 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107922307 | TGTGTCAGTATCCAG[A/G]AAAAAAAAATCACTG | 10451 |
rs78326196 | snp | C/G | 0.208474 | 0.246527 | intron-variant | VAV3 | GRCh38.p7 | 1:107834510 | AGTTATTTGATAACT[C/G]TACACAATAGCAGAA | 10451 |
rs78326676 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | VAV3 | GRCh38.p7 | 1:107930569 | AGGGTTACCTAGTCG[A/G]TAAGAAAAGATTCTT | 10451 |
rs78329309 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | VAV3 | GRCh38.p7 | 1:107703503 | TCATGCCAAGATCTG[C/T]CACTTTATAGCTGCT | 10451 |
rs78339294 | snp | C/T | 0.084728 | 0.187577 | intron-variant | VAV3 | GRCh38.p7 | 1:107900782 | TCACAATAGGGACTT[C/T]GTGGTCTCTGAACTT | 10451 |
rs78385372 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | VAV3 | GRCh38.p7 | 1:107745036 | TTGGATTTGGGGAAA[A/G]CATATCCATAGCTTC | 10451 |
rs78399732 | snp | A/T | 0.108755 | 0.206276 | intron-variant | VAV3 | GRCh38.p7 | 1:107944516 | TATGTTCAGTGCCTA[A/T]TGAGGGCTTTGAATA | 10451 |
rs78435278 | snp | A/G | 0.214843 | 0.247516 | intron-variant | VAV3 | GRCh38.p7 | 1:107804125 | ACTTTCAGCCTACAT[A/G]TGTCTTCATAGGTGA | 10451 |
rs78440599 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107679345 | TTATCAATTTAATCA[A/T]TACCTATTCATTTAT | 10451 |
rs78442648 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107874742 | TTTTTTGTTGTTGTT[G/T]TTTGGTTTTTGGTTT | 10451 |
rs78452835 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107805751 | TCTTTATTCCAGTCT[C/T]CTCTGTCTGGCTTGT | 10451 |
rs78453766 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107865721 | TAGTTAGATAGGCAA[G/T]AGTGGACAGGAAAGG | 10451 |
rs78458460 | snp | G/T | 0.389527 | 0.207442 | intron-variant | VAV3 | GRCh38.p7 | 1:107804977 | TTGGGTTTTTTTTTT[G/T]ATTCCCCTGGCAGCA | 10451 |
rs78484451 | snp | G/T | 0.319856 | 0.240042 | intron-variant | VAV3 | GRCh38.p7 | 1:107811845 | CCGAAAACTATCTTT[G/T]GACTTCTAGTAGGAA | 10451 |
rs78495697 | snp | C/T | 0.228547 | 0.249078 | intron-variant | VAV3 | GRCh38.p7 | 1:107813097 | GCACTCTAGCCTAAG[C/T]GACAGAGCCAGACTC | 10451 |
rs78499451 | snp | C/T | 0.230017 | 0.2492 | intron-variant | VAV3 | GRCh38.p7 | 1:107817167 | GACGCATTATGATAG[C/T]AGGCAGACAAAAAAT | 10451 |
rs78500683 | snp | C/T | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570868 | CTCCACTTCGGCCTT[C/T]GAAGTTCTCTTTAGA | 10451 |
rs78510461 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107654977 | AAATTGTGCCAAGAA[A/G]TTATAAATCATCTGG | 10451 |
rs78511608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862427 | AAAAAAAGAAGACAC[A/C]GAAAATAAACATGGA | 10451 |
rs78524975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107826513 | CAATAAAGTAAGTGT[C/T]GTTTTTGGAAAAAAT | 10451 |
rs78536939 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107904052 | CCCATTACCTGTTCT[A/G]TAACTTTCCACCTTA | 10451 |
rs78565142 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107855923 | CTCCTTCCACTTCTA[C/T]CCAGAAAACAGTGCA | 10451 |
rs78577193 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | VAV3 | GRCh38.p7 | 1:107889523 | GTGAACCAGGACAAT[G/T]GTCTTCCTACAGAAA | 10451 |
rs78605485 | snp | A/C | 0.0360489 | 0.129325 | intron-variant | VAV3 | GRCh38.p7 | 1:107649070 | CAAAAAACAAACAAA[A/C]AAAAAAAAAGCAAGC | 10451 |
rs78630499 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107841383 | AAAGCAATATAAAGG[A/G]CACAGAAATTGTCAG | 10451 |
rs78651845 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107795606 | GAATGATCTTTTAAG[G/T]TTATTTCCCCCAGAG | 10451 |
rs78672480 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107859088 | GTTTTTTTTTTTTTT[C/T]CATTTTTTGGTTTTT | 10451 |
rs78674280 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107891865 | AAAAAAAAAAAAAAA[A/G]AGCTCAGGGGTCAGA | 10451 |
rs78674521 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107924405 | GACAAAAAAAAAAAA[-/AA]CCCTGTAAACACTCA | 10451 |
rs78692758 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107957997 | CTGCTTTCCAGAGAA[C/T]CTAGGTTAAGCCACC | 10451 |
rs78697470 | snp | A/C/G | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107702884 | TACTGTGGTAAGAAT[A/C/G]AACATTATCTCACTG | 10451 |
rs78699917 | snp | G/T | 0.0463947 | 0.145069 | intron-variant | VAV3 | GRCh38.p7 | 1:107853690 | CACAGAAAGAGAAAA[G/T]CCAGAGAAACAAAAA | 10451 |
rs78700103 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896066 | CCACACACTTTCTCC[C/T]ATGGCCACAAGCACC | 10451 |
rs78704184 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107794018 | CTCTAGTTAATTACT[A/G]CGCAGAAGGCGCTTC | 10451 |
rs78704447 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107820491 | GGGGTAGGGTGTAGG[A/G]ATGGATAATAGTTAC | 10451 |
rs78713470 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107752019 | TGGAATCTCAAGGGA[C/T]TCTGAATAGTCAAAA | 10451 |
rs78726236 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950130 | CTGGAAACCACAAAA[A/C]AAAAAAAAAGTACTT | 10451 |
rs78730096 | snp | A/G | 0.089084 | 0.191327 | intron-variant | VAV3 | GRCh38.p7 | 1:107844316 | TTTCCCACTATCTTC[A/G]CAACCCAAAGAACAG | 10451 |
rs78739337 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107664944 | GAAAGAATTCAGTAC[A/C]TGTGGAAAATTACCA | 10451 |
rs78755947 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572644 | TTTTGTGTGCTTTTT[C/T]CACCTTTTATAAAGA | 10451 |
rs78765971 | in-del | -/AC | 0.234109 | 0.249494 | intron-variant | VAV3 | GRCh38.p7 | 1:107819548 | TATGACACAAATATG[-/AC]AAAGTGTTAATATCT | 10451 |
rs78786795 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107671835 | TATATTTGTTTAAAA[C/T]GTAATTTCCTATATA | 10451 |
rs78788276 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107808863 | TGCTGTATCAAAATA[C/T]TTATCCATATGCCTA | 10451 |
rs78809908 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107953128 | ACGGGAAACTTCACC[A/G]AATCTGGAATTAGGA | 10451 |
rs78810630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662590 | AAGAGTTGAATGGAT[G/T]TTATTCAAGGCCACT | 10451 |
rs78813663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962547 | ATTTCATAAGTCTCA[C/T]TAAAGGATTTAATGA | 10451 |
rs78822950 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107819759 | ATCAAGGAAGTATGA[C/T]GATTGTGGGATTAAA | 10451 |
rs78829564 | snp | A/T | 0.172997 | 0.237846 | intron-variant | VAV3 | GRCh38.p7 | 1:107671965 | TGTGGTTGTTATGCA[A/T]TAACAAAAAAGATAA | 10451 |
rs78830275 | snp | A/G | 0.11228 | 0.208646 | intron-variant | VAV3 | GRCh38.p7 | 1:107840595 | GCCTTTCTATGATCA[A/G]TCCATCAGGAAGTGC | 10451 |
rs78830402 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107792487 | TACTGCAGCTACCAG[A/C]AACTATGCATATAAA | 10451 |
rs78859375 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107905873 | GTAATAATCAAAAAA[C/T]TAACAAATAAATTCA | 10451 |
rs78862735 | snp | A/G | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688571 | TAGTAATTATTTTGC[A/G]ACCTTGGTTCTCTTA | 10451 |
rs78882173 | snp | C/T | 0.498109 | 0.0306926 | intron-variant | VAV3 | GRCh38.p7 | 1:107794354 | GATTCATCATTTTCT[C/T]CCTTCATCTTGCTTT | 10451 |
rs78890281 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107647592 | GTTCATATCTATAAA[A/C]ATTTTCAGAAATTTT | 10451 |
rs78898995 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107709124 | TGTAACATCTGATGC[C/T]GAGTTAAGTAGACCT | 10451 |
rs78911549 | in-del | -/A | 0.0711525 | 0.174681 | intron-variant | VAV3 | GRCh38.p7 | 1:107930142 | CAGGGTGACTGTAGT[-/A]AAAAAATAATTGTAC | 10451 |
rs78913972 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908007 | TTGTAAGTAGCATAC[A/G]TGTGTTGAGGAATGA | 10451 |
rs78916749 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | VAV3 | GRCh38.p7 | 1:107703777 | GATCCTTTCTTGTGT[C/T]CAAAAGTTTTACTGA | 10451 |
rs78920409 | snp | C/T | 0.277778 | 0.248452 | intron-variant | VAV3 | GRCh38.p7 | 1:107769675 | AATCCCATTCAAAGT[C/T]TAATAGGTATCACAA | 10451 |
rs78925391 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | VAV3 | GRCh38.p7 | 1:107663096 | TATAAACCAAAAAAC[A/G]TATTTAAGACTGGAA | 10451 |
rs78928729 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107670080 | GGGTGAGTATTTTCA[G/T]CTCCATTTTACAGAT | 10451 |
rs78940004 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107579438 | CCCATGTTTCCCCCC[A/T]GCAAGAACTCTCCTG | 10451 |
rs78951840 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107791689 | CCAGTGATTCTAGTA[A/T]GCAGCCAGGGTTGAA | 10451 |
rs78954198 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107753515 | ATATATATACACACA[C/T]ATATATATATACGTA | 10451 |
rs78966010 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107727788 | AACACTCAATCCCTT[A/T]CACTGAAATTTTATA | 10451 |
rs78967220 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107754984 | ATGGCATTTTTAACT[C/T]TTTTTTTTTTAAACT | 10451 |
rs78976892 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107764107 | AACAAAAAACAAAAC[A/C]AAAAAAAAAACATGA | 10451 |
rs78978583 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107911618 | TTCATTCTATTTTAA[A/G]GAAAAAATGTTCTAT | 10451 |
rs78982534 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107645333 | TGTATTTTTTTTTTT[G/T]TTGGTCATTTGTTAG | 10451 |
rs78993432 | snp | A/C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107915416 | GTTATGACTATCACC[A/C/T]CCATGTGATTTACTG | 10451 |
rs78998350 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | VAV3 | GRCh38.p7 | 1:107907593 | GTTATCAAAGGAGTG[A/G]ATTCATTACCACGAC | 10451 |
rs78998525 | snp | A/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107807444 | CTTTTAGAGATACTC[A/T]TAAAAGATTTGATTA | 10451 |
rs79013119 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107701108 | TATGTCTTCTTTTGA[A/G]AAGTGTTTGTTCATG | 10451 |
rs79041245 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107863696 | TATATCTTGGTATGT[A/C]TGTAAACCTCTGTGT | 10451 |
rs79054150 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107773914 | ACTGAAATTCATTTC[A/C]CTGGCACTCCTAATC | 10451 |
rs79062630 | snp | C/T | 0.202035 | 0.245356 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570707 | GGCAGTGTCCATCTC[C/T]GCCACTCCGGATTCG | 10451 |
rs79072056 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107811392 | AGCAGGCTGACATTT[C/T]ATTTTAAAATAGGAT | 10451 |
rs79073014 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107894971 | GCTATAAATTGTTTA[A/C]AACAGATCTCAGCCC | 10451 |
rs79099184 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107949313 | TTTTGTTTATTTTTG[A/T]TTGTTTGTTTGTTTT | 10451 |
rs79101088 | snp | C/T | 0.111224 | 0.207945 | intron-variant | VAV3 | GRCh38.p7 | 1:107904868 | TATTGATAAATGCTA[C/T]AGCATGGTTATATGC | 10451 |
rs79101907 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107814845 | AGAGAGAACAAGGAA[A/G]GAGAGATTATTGAGA | 10451 |
rs79108654 | snp | A/G | 0.178144 | 0.239451 | intron-variant | VAV3 | GRCh38.p7 | 1:107620755 | AAGCAGAGAAAAGAG[A/G]ATGAGAACCCAAAGA | 10451 |
rs79133696 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107701112 | TCTTCTTTTGAAAAG[G/T]GTTTGTTCATGTCCT | 10451 |
rs79146378 | snp | A/C/T | 0.0611083 | 0.163768 | intron-variant | VAV3 | GRCh38.p7 | 1:107842022 | ATTATTCTAGTTTCA[A/C/T]TACCTAGTAATAAAT | 10451 |
rs79169087 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107792628 | TTGGGTACAAATTTA[C/T]GTAAAATAAAATGTC | 10451 |
rs79210940 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107733191 | TCCTTTTTGTTGATG[G/T]TGATGTTATTCCTTT | 10451 |
rs79227180 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107732761 | CAGAGGTGGAGCCTA[C/T]AGAGGCAGGCAGGCC | 10451 |
rs79245617 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107871924 | GTAAACAACTTTAAC[C/G]ACCACTGGGCTGCAG | 10451 |
rs79271996 | snp | C/T | 0.2768 | 0.248559 | intron-variant | VAV3 | GRCh38.p7 | 1:107808148 | GAAGCTTTGCTGACA[C/T]ATTTCTCAAGGTTTT | 10451 |
rs79299414 | snp | A/G | 0.222035 | 0.248431 | intron-variant | VAV3 | GRCh38.p7 | 1:107771405 | CTACAGGTGCCCGCC[A/G]CCACGCCCAGCTAAT | 10451 |
rs79318742 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107845650 | GAGAACTTCCTGCAG[C/T]ATGTACAAGTATCAA | 10451 |
rs79327708 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107853973 | ACTGTATTTTTTTTT[C/T]CTAAGTTGGGATATT | 10451 |
rs79334501 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107825453 | AAAGATAGTACCCTC[A/G]CGGGAAAAAAAAAAA | 10451 |
rs79337747 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | VAV3 | GRCh38.p7 | 1:107833043 | GCAAAAAATCATAAA[A/G]ATAAAATAATTATGA | 10451 |
rs79343518 | snp | A/C | 0.498714 | 0.0253268 | intron-variant | VAV3 | GRCh38.p7 | 1:107701341 | CACCCTCTGAAGCAA[A/C]AGCCTGAGCTGTACG | 10451 |
rs79346709 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107897862 | TTTATTGCTGTACCT[C/T]ACTTTCTAAAATCCC | 10451 |
rs79361503 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107809909 | ATTTCCTAGAGAAAC[A/G]TTGCCAGGAAGGTTT | 10451 |
rs79372806 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107944857 | GCAATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 10451 |
rs79375406 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | VAV3 | GRCh38.p7 | 1:107812234 | GATACTGCTGGCAGA[A/G]TTGACACTCTTGTGC | 10451 |
rs79384734 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | VAV3 | GRCh38.p7 | 1:107744011 | TTAAATGTGATTTGT[A/G]GAGCTTAACGGCTAC | 10451 |
rs79384861 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107696613 | AAACATTATTGCTAT[A/G]AAGCTCTGTAAAGTA | 10451 |
rs79399511 | snp | C/T | 0.117537 | 0.212022 | intron-variant | VAV3 | GRCh38.p7 | 1:107957012 | TTGTTGGGTTTTAGG[C/T]ATTAGTAGAACAAAC | 10451 |
rs79421213 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107733107 | GAGTTTGCTGGAGGT[C/T]CACTCCAGACGCTGT | 10451 |
rs79425348 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107586157 | TTTTTTTTTTTTTTT[C/T]CCCAGAGCGCTCAGT | 10451 |
rs79444296 | snp | G/T | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570888 | TTCTCTTTAGAATAT[G/T]TGCTACTACCACCAA | 10451 |
rs79451333 | snp | C/T | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107821014 | TCATATATTGAGAGG[C/T]ACCTCTGACTCATGA | 10451 |
rs79454271 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | VAV3 | GRCh38.p7 | 1:107795339 | CCTTAACATATCCTC[A/G]GTGCTATATAAAAAC | 10451 |
rs79458835 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107805180 | TGTTTCTCTGACCTT[C/T]CTGTGCCTAAATTTA | 10451 |
rs79460078 | snp | A/G | 0.14665 | 0.227637 | intron-variant | VAV3 | GRCh38.p7 | 1:107950479 | TCTGGGATTTGGAGC[A/G]TTGGAACATGACCAG | 10451 |
rs79478107 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107840935 | TTAAAAAAAAAAAAA[A/T]TTCATCTGGCAATCA | 10451 |
rs79482905 | snp | G/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107842643 | AATGAGATTTCATTC[G/T]TCTTTTTTTTAAAAC | 10451 |
rs79483381 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107886266 | TACACATAACCCGAT[A/G]AAGAAGATGCCATTA | 10451 |
rs79486457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107878000 | TCCAGGACTTTTGCT[C/T]TGCTTTTACCAAACT | 10451 |
rs79510607 | snp | C/T | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570925 | CACCTGCGGCGGCTC[C/T]GCCCGGGCCCAGCCC | 10451 |
rs79511347 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897358 | CAGCTTTTCTCTACA[A/G]AGAAAACCATGAGAA | 10451 |
rs79513587 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107881158 | TTACTAGAGAGATGA[C/T]GTGGCATAGGAAGAC | 10451 |
rs79521845 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107856827 | GGATCACTTGAGCAC[A/G]GGAGTTCAAGACCAA | 10451 |
rs79537343 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786080 | TTAGCACCTCCTCTA[C/T]GGGCAAAGCAAAGCA | 10451 |
rs79547630 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | VAV3 | GRCh38.p7 | 1:107861856 | GCAAGGTAAAGCCTA[C/T]ACCTAAGGTCACCAA | 10451 |
rs79548971 | snp | C/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107804915 | ATATGTGAAGGATAG[C/T]GTTGTTGAAACAATA | 10451 |
rs79558587 | snp | C/G/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107727030 | AAAACATCATAACAA[C/G/T]GGTTGGGTAGAAATA | 10451 |
rs79561164 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902053 | ATCTCAAAAAAAAAA[-/A]ACAAAAAAAACAACA | 10451 |
rs79566197 | snp | A/G | 0.224709 | 0.248717 | intron-variant | VAV3 | GRCh38.p7 | 1:107860073 | TTCAGCAAAAATAGC[A/G]GTATATAAGTATTTA | 10451 |
rs79574171 | snp | A/C | 0.19646 | 0.2442 | intron-variant | VAV3 | GRCh38.p7 | 1:107617286 | GAAACCTGTACAATG[A/C]GTCTAATTTGTAGCT | 10451 |
rs79579575 | snp | C/T | 0.157972 | 0.232445 | intron-variant | VAV3 | GRCh38.p7 | 1:107865411 | TATGAGTGTAATGAG[C/T]GTATGTGATCTTGAA | 10451 |
rs79583906 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107615523 | CTAGGAAATACCATT[A/C]TTGACATAGGACCCA | 10451 |
rs79589127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107663174 | ATCTGAGGGTGATAA[C/T]TACCTAATGCAAAGT | 10451 |
rs79597802 | snp | G/T | 0.0711525 | 0.174681 | intron-variant | VAV3 | GRCh38.p7 | 1:107932723 | GGCAGAGTAAGATTT[G/T]ACCACAGAACAGGAG | 10451 |
rs79609252 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107753517 | ATATATACACACATA[C/T]ATATATATACGTATA | 10451 |
rs79638891 | snp | A/G | 0.109108 | 0.206518 | intron-variant | VAV3 | GRCh38.p7 | 1:107939888 | AAGCCCAGAGGAGGA[A/G]GAGTAAGACAGGACA | 10451 |
rs79643511 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107619172 | GAGGTGACTAGAGAA[C/T]CCATCCATACAACAC | 10451 |
rs79646870 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107577541 | CATACAACCAAGTTC[A/T]GGCCAATGGAATATA | 10451 |
rs79649532 | in-del | -/A | 0.435694 | 0.167385 | intron-variant | VAV3 | GRCh38.p7 | 1:107577019 | GACTCTTATAGCTGG[-/A]AAAAAGTAAATACAT | 10451 |
rs79650465 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107808617 | GCCCTCACAAGTCAC[C/G]TTCAATTCCAAAACA | 10451 |
rs79667292 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107940568 | TAAAGCTTAAAACTC[A/G]ATTGGGAGACAAGTA | 10451 |
rs79678344 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | VAV3 | GRCh38.p7 | 1:107723679 | GCTGCGCTAGTACCA[C/T]TAAGTACTGCTGCCA | 10451 |
rs79688416 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107667548 | TGATAAGGTTTATTG[C/T]TATCATTAGTGATGG | 10451 |
rs79697604 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702805 | TCTTTCAAAAAAAAA[A/C]AAAAAACCTGATTTT | 10451 |
rs79706698 | in-del | -/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107806523 | GTCTCCAATAATGGC[-/T]TTTTACTATCTTCAA | 10451 |
rs79722654 | snp | A/G | 0.0991586 | 0.199366 | intron-variant | VAV3 | GRCh38.p7 | 1:107938206 | TACCCTACAGAAGAG[A/G]AGGCGATCCCCGAGC | 10451 |
rs79725325 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107957893 | TCTTAAAAAAAAAAA[A/G]AGACACGATCTCATT | 10451 |
rs79727305 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | VAV3 | GRCh38.p7 | 1:107833091 | TTACATTAAGCTTAG[C/T]GAGGAAGGCATGTCA | 10451 |
rs79729985 | snp | G/T | 0.320335 | 0.239902 | intron-variant | VAV3 | GRCh38.p7 | 1:107804156 | GGTGGGTTTCTTCTA[G/T]GAAGCATATAGTTAG | 10451 |
rs79731296 | snp | A/G | 0.0718919 | 0.175435 | intron-variant | VAV3 | GRCh38.p7 | 1:107946878 | TAGTATTTAGTGGAA[A/G]GTGTTTTGCCACTCT | 10451 |
rs79748332 | snp | A/G | 0.266273 | 0.24947 | intron-variant | VAV3 | GRCh38.p7 | 1:107754654 | CATATTGGCCTACAA[A/G]GCTGTGTTATGTAAT | 10451 |
rs79762732 | snp | C/T | 0.109461 | 0.206758 | intron-variant | VAV3 | GRCh38.p7 | 1:107957998 | TGCTTTCCAGAGAAC[C/T]TAGGTTAAGCCACCA | 10451 |
rs79765119 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107860096 | AGTATTTATAATAGA[C/T]AGTAGATGAATCAAA | 10451 |
rs79770306 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107923558 | GAGGCTTCCCCAGCC[A/G]TGTGGAACTGTGAGT | 10451 |
rs79783202 | snp | G/T | 0.5 | 0 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107704999 | CAGGATGTGACTCGA[G/T]TGAAGGTATGCATCT | 10451 |
rs79786588 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107858455 | AAACTTCTAGAACAG[A/G]GGTCCCCAACCCCCA | 10451 |
rs79803135 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107730239 | GACAGCATTATCATA[C/G]TGTGTCCATACCTTC | 10451 |
rs79807732 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107929287 | AGTGACACTCTGTCT[A/C]AAAAAAAAAAAAAAA | 10451 |
rs79821121 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107670091 | TTCATCTCCATTTTA[C/T]AGATTAGAAAACTGA | 10451 |
rs79843746 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107703831 | AACACAGAGAAACTC[A/G]GGGGAAAAGGACAAA | 10451 |
rs79907975 | snp | A/C | 0.0486741 | 0.148216 | intron-variant | VAV3 | GRCh38.p7 | 1:107668226 | CCTGGCTAAAAAATA[A/C]ATCTTCTGATAAAGT | 10451 |
rs79911555 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107760040 | CAAAAATAGAGATGA[A/C]TAATAATTTTGCAGC | 10451 |
rs79912592 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | VAV3 | GRCh38.p7 | 1:107953716 | TGTTCCCATTAAACC[A/G]TGCTGCCCCCATGCT | 10451 |
rs79916724 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107796803 | TGTAAAAAAAAAAAA[A/T]AATATATATATATAT | 10451 |
rs79916975 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | VAV3 | GRCh38.p7 | 1:107658082 | TCTCTTTCTAATGAA[A/G]GAAAACCGTACTTCC | 10451 |
rs79954099 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962810 | AGTGCAACGGCACAA[A/G]GAAGGTCATTAGCTG | 10451 |
rs79964079 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594112 | ACGAATGACTAATCT[C/T]GGAGTGTTAACCACT | 10451 |
rs79970591 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107860561 | CAAACCACTTGGTAT[A/G]ATGATAGTGTCCCTT | 10451 |
rs79990284 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | VAV3 | GRCh38.p7 | 1:107807530 | AAACAAGAGCAGGGT[C/T]GTAGTGCTCCAGGGC | 10451 |
rs79996958 | snp | A/C | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688574 | TAATTATTTTGCAAC[A/C]TTGGTTCTCTTACCC | 10451 |
rs80007339 | snp | A/G | 0.095934 | 0.196885 | intron-variant | VAV3 | GRCh38.p7 | 1:107802528 | CCTTCTATTCTTAAC[A/G]TTTGTTGAGGATTTT | 10451 |
rs80015082 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107801924 | CTCTTCAATTTCTTT[C/T]GTCAGCATTTTTTTA | 10451 |
rs80042921 | snp | A/C | 0.186421 | 0.24178 | intron-variant | VAV3 | GRCh38.p7 | 1:107942287 | CAGGACAGATGTAAA[A/C]CCTGGTGAGATCCCA | 10451 |
rs80089293 | snp | C/T | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570753 | TCCCTTTCGATTGGC[C/T]GAGGGCAACAGAGGC | 10451 |
rs80105082 | snp | C/G | 0.5 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107571001 | CGTCCACGGGGCTGG[C/G]GGGCGGGGGGGTGGT | 10451 |
rs80127119 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | VAV3 | GRCh38.p7 | 1:107638397 | TATATCTCACAATGA[A/G]CAACATAAATTAAAA | 10451 |
rs80142139 | snp | A/G | 0.0926964 | 0.194308 | intron-variant | VAV3 | GRCh38.p7 | 1:107654097 | CTAAAAGCAAAAGTG[A/G]TGTTCTTTCCAAAAA | 10451 |
rs80156559 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107574408 | TAAGTTTAAAGAACC[A/G]TTGTCCTGTTTTTCC | 10451 |
rs80163255 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107869371 | CTCTTGCACTTAATT[A/C]AAAATTCGACACCTA | 10451 |
rs80164968 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | VAV3 | GRCh38.p7 | 1:107818384 | TTTTTTTTTAAACCA[C/T]AAAATGCTGATCATG | 10451 |
rs80166450 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107707448 | TGCTTAGAACACTGC[C/T]TGACCCATATTTGGT | 10451 |
rs80173139 | snp | A/G | 0.228842 | 0.249103 | intron-variant | VAV3 | GRCh38.p7 | 1:107822516 | AAAAAACAGCCGGGC[A/G]AGGTGGCGGGTGCCT | 10451 |
rs80174334 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107693350 | AAGTTGCATAGTTTG[C/T]CTTATTAACAAAATA | 10451 |
rs80222513 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107764117 | AAAACAAAAAAAAAA[A/C]CATGATGTACAAAAA | 10451 |
rs80227161 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | VAV3 | GRCh38.p7 | 1:107917398 | GTAGGAATTTTATAG[A/G]TAAGGGAACTAAGAT | 10451 |
rs80235198 | snp | G/T | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107804008 | CACCTTCTCTATTAG[G/T]CAGAGTCTAAAGTCT | 10451 |
rs80236271 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107764762 | CTTCTTACTATCTAC[A/G]CAAGTTATTCATAAT | 10451 |
rs80236511 | snp | A/C | 0.120326 | 0.21374 | intron-variant | VAV3 | GRCh38.p7 | 1:107960449 | CCAACTTGGGCTACA[A/C]AGTAAGACTCCGTCT | 10451 |
rs80243819 | snp | A/G | 0.276267 | 0.248616 | intron-variant | VAV3 | GRCh38.p7 | 1:107798576 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGTGGGC | 10451 |
rs80255118 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107775962 | TCTAGAATAAGAGGT[A/G]TCTGAGTTCAAATCC | 10451 |
rs80268143 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | VAV3 | GRCh38.p7 | 1:107744441 | AACTGGGCCAAGGTC[A/G]GTCAGAAGAAATTCT | 10451 |
rs80293194 | snp | A/T | 0.189261 | 0.242509 | intron-variant | VAV3 | GRCh38.p7 | 1:107662471 | TAAGTTATCTCTCTC[A/T]CACACACACACAGTG | 10451 |
rs80321534 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107876197 | ATCAGATGCTGCAGA[C/T]GGCCAAATAGGATTT | 10451 |
rs80340372 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107861720 | ATAAATATGCAGCTA[C/T]TTTAAAAGACAACTC | 10451 |
rs80345374 | snp | A/G | 0.030278 | 0.119257 | intron-variant | VAV3 | GRCh38.p7 | 1:107708015 | CAAATCTACAAGGCA[A/G]AGTCATTCATCCATT | 10451 |
rs80350363 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | VAV3 | GRCh38.p7 | 1:107823622 | TGGTAGGAAAGTCAC[A/G]AGACTGTCTGTTAAT | 10451 |
rs80350376 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107844301 | CCCAGATACTATGTT[C/T]TTCCCACTATCTTCG | 10451 |
rs80353498 | snp | C/T | 0.319616 | 0.240112 | intron-variant | VAV3 | GRCh38.p7 | 1:107804122 | ATTACTTTCAGCCTA[C/T]ATGTGTCTTCATAGG | 10451 |
rs111234212 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107778411 | ATGCTTTAAAAAAAT[C/G]TTTACATATAATAAC | 10451 |
rs111257483 | in-del | -/CTCC | 0.490063 | 0.0697833 | intron-variant | VAV3 | GRCh38.p7 | 1:107664338 | ATTATTCCTGATGCT[-/CTCC]CTCCCTCCCCAACCC | 10451 |
rs111273924 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928889 | GAAAGATATCGATAT[C/G]CAAGTATAATAAGGT | 10451 |
rs111274414 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107942850 | TAAGGGCCACCCCCA[A/T]TCCTTTTTATCTGCT | 10451 |
rs111282763 | snp | A/C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107950478 | GTCTGGGATTTGGAG[A/C/T]GTTGGAACATGACCA | 10451 |
rs111285946 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107744320 | CTGTGCCAGGCACTT[A/T]TTACACAGTCGAGAA | 10451 |
rs111290722 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | VAV3 | GRCh38.p7 | 1:107908531 | CCTTTTTATTCTTAT[C/T]AACATTTTCTGGCTT | 10451 |
rs111312401 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959282 | AAATAAATTAATTAA[C/T]TAATTAATTAACCCA | 10451 |
rs111329884 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107932531 | CTGTAAGTATGCTGG[C/T]AGGCTGAATAATAGC | 10451 |
rs111333369 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107751801 | AGAGGCTGATAACTA[A/G]ATTATTTTTAAGTGT | 10451 |
rs111348832 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | VAV3 | GRCh38.p7 | 1:107801368 | CTGATATTTTGATAA[A/G]GACTGCATTGAATCT | 10451 |
rs111349034 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107862241 | AGTGACTGCCAAGCA[C/T]TGTTTCCTGTAGTTG | 10451 |
rs111360615 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107712376 | AAGCTCATCAGCTAT[C/T]GTTATTGTTAGTGTA | 10451 |
rs111380884 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107607990 | CATTTTGTTCCCTAG[C/T]AGAAGACATTTCACA | 10451 |
rs111384525 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107777173 | CATCCACAGTTAAAA[C/T]CCACAATGGACACAT | 10451 |
rs111391142 | snp | A/G | 0.0539704 | 0.155153 | intron-variant | VAV3 | GRCh38.p7 | 1:107736242 | TATGACAAACCCACA[A/G]CCAATATCATACTGA | 10451 |
rs111393436 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107874643 | TTCCCTCCCTGTATA[C/T]TATTTTAATTACAAA | 10451 |
rs111393520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107905523 | CCAATGCTAAAGACC[A/T]CTGACATCTTAAAAA | 10451 |
rs111399031 | snp | A/G | 0.104859 | 0.203554 | intron-variant | VAV3 | GRCh38.p7 | 1:107907655 | CTTGCTCTCGTGTGC[A/G]TGCGTTCTCTCTCTC | 10451 |
rs111437387 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107873500 | GCAGGAGGAACAGGC[A/G]GAAGGATAAAAGAAA | 10451 |
rs111474431 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | VAV3 | GRCh38.p7 | 1:107605810 | CCTGAATATATCTCA[C/T]GATGTTTATGCAAAT | 10451 |
rs111482001 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107663635 | AGAAAAAAATGCCAA[C/T]TTGCAAAATGAAGCA | 10451 |
rs111499251 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107849597 | ATTAAAGACTTAAAC[A/G]TAAGACCTAAAACCA | 10451 |
rs111518583 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107958539 | CTGTATGAAAACACA[C/T]GGCAATCAATGACTC | 10451 |
rs111519631 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | VAV3 | GRCh38.p7 | 1:107615351 | CGTTCTCACTTGTAA[A/G]TGGCAGCTAAACATT | 10451 |
rs111520150 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107781542 | GTTAATTTTTAAAAA[A/T]TTAAGAAAATTTGTT | 10451 |
rs111529064 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107804966 | GGGGTGGGGGTTGGG[-/T]TTTTTTTTTTGATTC | 10451 |
rs111537116 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107657988 | GTTTTTATTTTGGCA[A/T]AGAATTTATATGAGG | 10451 |
rs111538706 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107912315 | GGAAGAAACCTCCAA[C/T]AAGCTCAGGTTTTAA | 10451 |
rs111554726 | snp | A/G | 0.0737376 | 0.17729 | intron-variant | VAV3 | GRCh38.p7 | 1:107659280 | AATACCATCTTTCAG[A/G]AAAAAAAAAGTATAA | 10451 |
rs111559364 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107904480 | TGAATTTTTTTATTT[A/C]TTTTCTTATTTGACT | 10451 |
rs111567893 | snp | C/G | 0.234982 | 0.249549 | intron-variant | VAV3 | GRCh38.p7 | 1:107583312 | AGATCATACTGAATG[C/G]GAAAAAACTGGAAGC | 10451 |
rs111570831 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107617487 | CTGACCTGGCCAGTA[C/T]CCTTTGTAGATTTTT | 10451 |
rs111571934 | snp | C/G | 0.278664 | 0.248351 | intron-variant | VAV3 | GRCh38.p7 | 1:107634797 | AACAAACAACCCCAT[C/G]AAAAAGTGGGCAAAG | 10451 |
rs111587375 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107956889 | ACAAGCAGGACAAAT[C/T]GAGGGACGTCAAGGA | 10451 |
rs111594503 | snp | A/G | 0.216048 | 0.247684 | intron-variant | VAV3 | GRCh38.p7 | 1:107952417 | ACCCCCATGACACAC[A/G]TTTACCTATGTAACA | 10451 |
rs111615451 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107737803 | ACAGTGTGGCGATTC[C/T]TCAATGATCTAGAAC | 10451 |
rs111616725 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107632385 | GGTATAGCCCCACTC[A/G]GGTAATACATGAAGA | 10451 |
rs111643416 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107905532 | AAGACCTCTGACATC[A/T]TAAAAAAAAAATCTA | 10451 |
rs111676506 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107912211 | ACAAAAAAATAACAA[C/T]TTCAAAGGCAGACTA | 10451 |
rs111706551 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107845674 | GTATCAACAGCCAAA[C/T]AGATCAAACAGAAGA | 10451 |
rs111729848 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | VAV3 | GRCh38.p7 | 1:107585487 | AAAGCTAAAGTCCTT[C/T]AGGGCCTTAAGTGAT | 10451 |
rs111730892 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107962235 | ATCTCTAACTCCAGG[A/G]GAATACATTCTGCTG | 10451 |
rs111732589 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107955472 | GGAACTAGCCTATGG[A/C]ATCCTCAATCAAGCC | 10451 |
rs111733432 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | VAV3 | GRCh38.p7 | 1:107573528 | AACTGCTCTTAGAAG[C/T]CTAATAGAGTAAATG | 10451 |
rs111756353 | snp | A/T | 0.14933 | 0.228835 | intron-variant | VAV3 | GRCh38.p7 | 1:107922944 | GCGACAGAGCGAGAC[A/T]CCGTCTCAAAAAAAA | 10451 |
rs111780755 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107789340 | CAGAAAGTCTCAGAA[A/T]GAAAAGGCCAGAACG | 10451 |
rs111786811 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107868693 | ATCTCCTCTTGCATA[C/T]ACGATAGGAGATGTA | 10451 |
rs111787688 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | VAV3 | GRCh38.p7 | 1:107619704 | AAAGTGTATTTGAAG[A/G]TGTATCAACAAATTG | 10451 |
rs111797557 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952488 | TATATATATATATAC[A/G]CACATAAATTCAACC | 10451 |
rs111816115 | snp | A/G | 0.0744748 | 0.178019 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592622 | CACCAATCTGTTAAC[A/G]TTACCTTACCTGCTT | 10451 |
rs111817564 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107931643 | CACGTGATTGAAATA[C/T]TGTCATAAAGAATTG | 10451 |
rs111820405 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107887469 | CAACACATAAAATCT[A/G]CAACCATTCATTCTG | 10451 |
rs111824055 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107674100 | GGTAGTTTTTCAGAA[C/T]TGCATGATATTTAAA | 10451 |
rs111825067 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897474 | CCCAGAAAGGGCATA[C/T]GGAAAGCTGAGAATG | 10451 |
rs111829952 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | VAV3 | GRCh38.p7 | 1:107733506 | GAAAAAAGATTAGAC[A/G]AATGGCTAACTAGAA | 10451 |
rs111839699 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107674070 | CCAAAAGCCAACACT[A/G]CAAAATAATCTGAAG | 10451 |
rs111849398 | snp | C/T | 0.138207 | 0.223612 | intron-variant | VAV3 | GRCh38.p7 | 1:107834451 | AATAACTACAGGAAA[C/T]TGGAATATTCAATTG | 10451 |
rs111851142 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107849127 | AGAAAGAATCAATAT[C/T]GTGAAAATGGCCATA | 10451 |
rs111860509 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107877857 | TTAGTGCTGAGTCTA[G/T]TGCGAGCCTAGTGTT | 10451 |
rs111861964 | snp | A/T | 0 | 0 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896709 | TTAAAAAGACTGGCA[A/T]TTTTGTTATTAATCA | 10451 |
rs111863673 | in-del | -/G | 0.5 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570724 | CGCCACTCCGGATTC[-/G]GGGATCTGAACCGGA | 10451 |
rs111868986 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107794242 | TGGCCCAGGAGTAGC[A/C]TGGTTTCCACTGAGG | 10451 |
rs111878582 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107647776 | TTTGCTTTTGAGAAA[A/G]TTACAGTGAAATAAG | 10451 |
rs111952693 | in-del | -/GT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107753484 | TATGTATGTGTGTGT[-/GT]ATATATATACACACA | 10451 |
rs111962195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757483 | TCCATCAAAAATTTC[A/C]AACTGTAAGAAGACC | 10451 |
rs111965870 | in-del | -/AACCAC | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107928190 | CTACAACTCTACAAG[-/AACCAC]AGCATTACTGGGTTT | 10451 |
rs111977751 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107903195 | CTGAGCAGTTGGTTC[A/C]TAAGAAAAAAGCACC | 10451 |
rs111984986 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107919795 | TTATGAAATCACCAT[A/C]AACCATGTGGTATCT | 10451 |
rs111991231 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107757179 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTATGCAA | 10451 |
rs112007038 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107797690 | TCTTAAGAAAAATCA[C/T]GTTATGCCTCAGTAA | 10451 |
rs112008374 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107920441 | CAAACAAAAACTTAC[A/G]GGTGGTCCACCAAAT | 10451 |
rs112008728 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107767044 | GTGCCTAATGTTTTA[C/T]TGACAGGATAAAATA | 10451 |
rs112063628 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107841572 | TGCCCCAATTTAAAA[C/T]AGGTATCATTAACAT | 10451 |
rs112107766 | snp | C/T | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573216 | AAGGAGGGAGGATGT[C/T]GAACAGCCAGAAATG | 10451 |
rs112123390 | snp | C/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107660200 | ACCCTGCAATGCTCA[C/G]AAAGGGAGATTCCTT | 10451 |
rs112127049 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107938396 | CTCAAGGGAGGAAAC[C/T]ATCAGGACCACAGGG | 10451 |
rs112127778 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753526 | CACATATATATATAT[A/G]CGTATATATATATAT | 10451 |
rs112132696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107683346 | TTTACACGTTAGACC[A/G]TGACCTCCTGGTCAC | 10451 |
rs112140816 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107840921 | TTCAGAGATGCTTTT[-/A]AAAAAAAAAAAAAAT | 10451 |
rs112152324 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107701075 | AGCTTTTTTTTTCAT[A/G]TATGTGTTAGCTGCA | 10451 |
rs112152649 | in-del | -/ATTAAGGGTCCTAC | 0.10237 | 0.201756 | intron-variant | VAV3 | GRCh38.p7 | 1:107951093 | TCCAGTACTAATGTT[-/ATTAAGGGTCCTAC]ATCATCGTTCAGAAT | 10451 |
rs112168571 | snp | A/C/T | 0.0131032 | 0.0799785 | intron-variant | VAV3 | GRCh38.p7 | 1:107681754 | TGCCTCCCGGGCTCA[A/C/T]GCCATTCTCCTGCCT | 10451 |
rs112186876 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107634402 | AATAAATGGTGCTGG[G/T]AAAACTGGCTAGCCA | 10451 |
rs112202412 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107683721 | TAGTAAGTCTTCCAC[A/G]TGTATATCATTACAC | 10451 |
rs112203125 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | VAV3 | GRCh38.p7 | 1:107713300 | ATCTTTAAAGGAAAT[A/G]AAAGCAAACAAAAGA | 10451 |
rs112210620 | snp | A/G | 0.444444 | 0.157135 | intron-variant | VAV3 | GRCh38.p7 | 1:107732290 | TCTGCAGCTCCCAGC[A/G]TGACTGACGCAGAAG | 10451 |
rs112213848 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702646 | CAATGATTTCCTATT[G/T]ACTTTTATAACGTAA | 10451 |
rs112216180 | snp | C/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107710347 | AAAGTAGGAGAGCTG[C/G]AAGCAAATGTCAGTG | 10451 |
rs112225044 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107927418 | TTGAAAAAAGAAGAG[G/T]AAATAGCAAAGGGGA | 10451 |
rs112232624 | in-del | -/AAC | 0.235564 | 0.249583 | intron-variant | VAV3 | GRCh38.p7 | 1:107955277 | TTAGTAATGGCACTT[-/AAC]AAGTATTTTTGGTTT | 10451 |
rs112245262 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107738487 | GAAATGCACAATACA[C/T]AGTCTTATTCAAAAA | 10451 |
rs112263179 | snp | A/C/G | 4.94442e-05 | 0.00497188 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107772832 | TCTTCTTCATCTTCC[A/C/G]CAAGGGTTTCACTAC | 10451 |
rs112267134 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107766999 | TTTTGTTTTATAATC[A/C]CTGTAAATTTTTTAA | 10451 |
rs112267287 | in-del | -/GT | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107814003 | TGTGTGTGTGTGTGT[-/GT]GTGTGTGTGTGTATA | 10451 |
rs112277349 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902084 | ACAAAAACTGTTATT[G/T]TTTTGGCCTGCAAAA | 10451 |
rs112302403 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107760335 | TCAAAATAAATGTAG[C/T]CTTATTATAATTTAG | 10451 |
rs112304960 | snp | C/T | 0.206947 | 0.246265 | intron-variant | VAV3 | GRCh38.p7 | 1:107958634 | ATTTTACTTATTTTT[C/T]TTTATCATTATACTT | 10451 |
rs112308282 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107910105 | GCATGATTATCCTCA[C/T]TTTACAGAAGAGGAA | 10451 |
rs112314190 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107862341 | AGTTCCACCCCCACA[C/T]TACCCCTCTCACTGA | 10451 |
rs112323074 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107783892 | TCTCTACTAAAAATA[C/T]AAAAAAAAAAAAAAA | 10451 |
rs112323477 | snp | C/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107686037 | TGGTTGGGGGGGTGG[C/G]GGGGGAGGGGGGGCA | 10451 |
rs112326347 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107907994 | ATTAAGTGTTCAGTT[G/T]TAAGTAGCATACGTG | 10451 |
rs112335447 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107586670 | AATTGATTAATTATT[C/T]TGAAAAAGAAAAGGA | 10451 |
rs112349756 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107770438 | TTACTATATCCTTAG[C/T]CCCTGAAACAGTGCC | 10451 |
rs112355991 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107852851 | TTTATCAGCAACCAC[G/T]CTATCTAAAAGAGTG | 10451 |
rs112391856 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107666126 | AGCCCTTCACCTTAC[C/T]CTTCCTCTTCACTGT | 10451 |
rs112392568 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107664676 | GGAGCTTATGAAAGA[C/T]TGCAGAAAGTAGATG | 10451 |
rs112443956 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | VAV3 | GRCh38.p7 | 1:107643998 | TTCTGTTCTTGTGCC[A/G]CAGAACCCCCAGAGG | 10451 |
rs112445262 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107850576 | GGGCCTGTCGAGGGG[A/T]GGGGGGCAAGGGGAG | 10451 |
rs112446361 | snp | A/G | 0.0577344 | 0.159793 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594500 | TCTCTTAAAAAGACT[A/G]GATAGGGAAGTTTGA | 10451 |
rs112449106 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107644234 | TGCTACTGCTAATTT[A/T]AAATGAAACCTAAAT | 10451 |
rs112453779 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107761243 | AAATACAAAAACAAA[A/G]TTAGCCGGTCATGGT | 10451 |
rs112454462 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107711849 | CACTAGCATGCCTGG[C/G]CAATTTTTGTATTTT | 10451 |
rs112495050 | in-del | -/GGAT/GGATGGAT | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107630348 | GAAGAATGGATGGGA[-/GGAT/GGATGGAT]GGATGGATGGATGGA | 10451 |
rs112516584 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | VAV3 | GRCh38.p7 | 1:107609742 | GCATGCACACACACC[C/T]CCCTCGCAGATAAAG | 10451 |
rs112518616 | snp | C/T | 0.444444 | 0.157135 | intron-variant | VAV3 | GRCh38.p7 | 1:107704805 | CTTCTGAAAGGACTG[C/T]CCAGGCAGAAAGCCT | 10451 |
rs112524940 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107770441 | CTATATCCTTAGTCC[C/T]TGAAACAGTGCCACT | 10451 |
rs112526196 | snp | A/T | 0.0314385 | 0.121371 | intron-variant | VAV3 | GRCh38.p7 | 1:107615817 | TTTGGAAAGAAGACA[A/T]ACATATAATTGGCCA | 10451 |
rs112528733 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753525 | ACACATATATATATA[C/T]ACGTATATATATATA | 10451 |
rs112536614 | snp | A/G | 0.145978 | 0.227331 | intron-variant | VAV3 | GRCh38.p7 | 1:107761250 | AAAACAAAATTAGCC[A/G]GTCATGGTGGCAGGT | 10451 |
rs112545452 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107955564 | CTACCAGACACTGTG[C/G]CACAAAGCAGCATGT | 10451 |
rs112550014 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107716533 | TTATGTGATGGATTA[C/T]GTTTATTCATTTGCA | 10451 |
rs112554691 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107944906 | CGACTGTGCCCAGCC[A/C]CAAAATGCAGTTTTG | 10451 |
rs112562360 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107771501 | CTCATGATCTGCCTG[C/T]CTCGGCCTCTCAGAG | 10451 |
rs112570449 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107722843 | CTATTATCCTCTCTT[C/T]TTTTTTTTTTTTGTA | 10451 |
rs112590700 | snp | A/T | 0.228547 | 0.249078 | intron-variant | VAV3 | GRCh38.p7 | 1:107820073 | AAAAAACTAAAAATA[A/T]AACTACCATATGATC | 10451 |
rs112615329 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107642533 | TTGCTTTGCACTGTG[A/G]ACTCGCCCTGAATTC | 10451 |
rs112647722 | snp | A/G | 0.0704125 | 0.17392 | intron-variant | VAV3 | GRCh38.p7 | 1:107603891 | CTGCCTGCAACCTCC[A/G]CCTCCTGGGTTCAAG | 10451 |
rs112648831 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107581868 | CTAATCGACACTCTT[C/T]GTTCAGGTACTAGTT | 10451 |
rs112658990 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107733059 | TCTACAAAATTTGCT[A/G]TTCTGCAGCCTCTGC | 10451 |
rs112665496 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | VAV3 | GRCh38.p7 | 1:107600709 | GGAACTCATGTATCT[A/G]TGTCTACCAATCCAG | 10451 |
rs112688161 | in-del | -/T | 0.0314385 | 0.121371 | intron-variant | VAV3 | GRCh38.p7 | 1:107697262 | ACCCCGATCTGAGAG[-/T]TAAAAAAAGGAAGCC | 10451 |
rs112693401 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107641760 | TGAAGTGAACTGTTA[A/C]TATATTAAAGCCATG | 10451 |
rs112717784 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107935064 | ATGGGGCAAGTTTCC[A/G]GTTGGCAAACATTCA | 10451 |
rs112731348 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107699421 | TATGGCGTTGCAGGG[C/T]ACAGCCCCCCTCCTG | 10451 |
rs112747850 | snp | C/T | 0.215747 | 0.247642 | intron-variant | VAV3 | GRCh38.p7 | 1:107952399 | AAATAATCTGCACAA[C/T]AAACCCCCATGACAC | 10451 |
rs112797988 | in-del | -/A | 0.298398 | 0.245271 | intron-variant | VAV3 | GRCh38.p7 | 1:107836932 | AAGAAACCTACCAAC[-/A]AAAAAAAACAGGTGG | 10451 |
rs112824602 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | VAV3 | GRCh38.p7 | 1:107733833 | CAAGATATTAACCAG[A/G]AGGACGTCCCCAACC | 10451 |
rs112830066 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107863761 | TTTTTTTAAAAAACT[A/C]CCCGAAAGATTCACT | 10451 |
rs112837004 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107748899 | TAGAGTACACTTATT[A/G]GTTGTTCATTATTCA | 10451 |
rs112854271 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107849582 | CAAAAATTAAGATGG[A/G]TTAAAGACTTAAACA | 10451 |
rs112857293 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | VAV3 | GRCh38.p7 | 1:107633774 | GAAGTCTAAGTACCC[C/T]GCGATCACCATGCTG | 10451 |
rs112863402 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107603348 | TCCAAACACAAATGC[C/T]CTACAAAACTAACAA | 10451 |
rs112865057 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107740334 | GCTGACTACTGAATA[C/G]AGAAAAAGTTACTAC | 10451 |
rs112865898 | snp | C/G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107630038 | GTACAAAAGACATTT[C/G/T]TGAAATCAAATACAA | 10451 |
rs112871613 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107575970 | CTTTTCAAGTAATGT[A/G]TACTGAATTTTACTT | 10451 |
rs112875324 | in-del | -/A | 0.489608 | 0.0713316 | intron-variant | VAV3 | GRCh38.p7 | 1:107735632 | TAAATTCCTAGACAC[-/A]TACACTCTCCCAAGA | 10451 |
rs112878643 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107706130 | ATCAGGGGTACACCT[A/C]GAAAGCTAAAATGAT | 10451 |
rs112898806 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107757181 | TGTGTGTGTGTGTGT[A/G]TGTGTGTATGCAATT | 10451 |
rs112899926 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107723909 | GACATTGGATAAATA[C/G]AGAACACATCGTAAA | 10451 |
rs112909720 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107949930 | TATCAGGTATTGCCT[A/G]TATGATTAAAAGAAA | 10451 |
rs112916345 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786513 | AAGTTTACTTTCAGC[A/G]TTAAAGAGGTGACAG | 10451 |
rs112920841 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107832664 | AGGTGTCTTTAACAC[A/C]TCGGTAGAAATGGCT | 10451 |
rs112937517 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107779962 | GCCACACACATGTGG[A/C]CACTGTAATGAACTA | 10451 |
rs112938969 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107638878 | AACAGACCTACATAT[A/G]CATATATATGAAGAT | 10451 |
rs112951600 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107947640 | GCCCACAGCCATTCA[C/T]CTAATGGTGCATGAG | 10451 |
rs112961954 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | VAV3 | GRCh38.p7 | 1:107606679 | TTAACTTATAAGAGC[C/T]CCTTTTTATTTTGAC | 10451 |
rs112965883 | snp | A/G | 0 | 0 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573221 | GGGAGGATGTTGAAC[A/G]GCCAGAAATGCAGCT | 10451 |
rs112975691 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107926208 | AATGACTTGAACCCG[A/G]GAGTGGAGGTTGCAG | 10451 |
rs112976590 | snp | C/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107651329 | ACACTCCTTTAGATA[C/G]TCAATCTTCTTGCTT | 10451 |
rs112981901 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107852338 | AGTATTTTTAAAAGA[A/C]AATGAGTCTCCAATT | 10451 |
rs112983692 | snp | C/T | 0.5 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570803 | ATGGCGCTCACCTAT[C/T]TCTCAGGACCGAATG | 10451 |
rs112984085 | snp | C/G | 0.136151 | 0.222572 | intron-variant | VAV3 | GRCh38.p7 | 1:107576385 | AATAAAAGTAGTAAA[C/G]CAGTACCTGACCAGA | 10451 |
rs112984919 | snp | C/T | 0.084364 | 0.187256 | intron-variant | VAV3 | GRCh38.p7 | 1:107907652 | CCTCTTGCTCTCGTG[C/T]GCGTGCGTTCTCTCT | 10451 |
rs112990500 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107733255 | TCATCAAAGACCAAA[C/G]GTAGATAAAAACCAC | 10451 |
rs113000017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107855311 | AGACAGAGTCTTGCT[C/T]TGTCACCCAGGCTAA | 10451 |
rs113000897 | snp | A/G | 0.235273 | 0.249566 | intron-variant | VAV3 | GRCh38.p7 | 1:107954622 | ATCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG | 10451 |
rs113010952 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107607635 | TACCATGGGAAAAGG[A/C]AGGGACCCTGACATC | 10451 |
rs113019808 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107827290 | TTCCCTTCTCTCAAA[G/T]CCCTCTTCCTTCCTT | 10451 |
rs113023728 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107663558 | AGCTAGAAGAATGTA[A/C]TAAGCAGACTTACAT | 10451 |
rs113034334 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107933634 | GCCTGGGGAATGCAC[G/T]GAGACCCCATCTCTA | 10451 |
rs113044186 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107905772 | TTGCTTTCTAAGACA[C/T]AGAATATTTTATCTT | 10451 |
rs113045134 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107728600 | ATATGTATACGTATA[C/T]GTATATGTATATGTA | 10451 |
rs113054892 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107764106 | AAACAAAAAACAAAA[A/C]AAAAAAAAAAACATG | 10451 |
rs113063097 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107640961 | GATGGAATACGGGAT[A/G]AAAAGTCCAAGAAGA | 10451 |
rs113066279 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107844835 | TAAAACTCCCATCTC[C/T]CTGGGACAGAGCACC | 10451 |
rs113074950 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107629719 | CTCAATTGATAATTC[A/T]TTGTTTGAAAGAAGT | 10451 |
rs113080726 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107654067 | AAGCAACTTAAGTCC[A/G]GTTGCATATTCTAGC | 10451 |
rs113097877 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755757 | TGAGAAGAGTCAGGA[C/T]GTTGTTGCCTTAAAA | 10451 |
rs113102217 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107583134 | ATGGTATCTCACTGT[A/G]GTTTTGATTTGCATT | 10451 |
rs113108314 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107643006 | CATCAATCTCTTTTT[C/T]AGTTGAAAAAATATT | 10451 |
rs113111040 | snp | A/G | 0.0733688 | 0.176922 | intron-variant | VAV3 | GRCh38.p7 | 1:107662727 | ACTTCCCAGAAAAAC[A/G]CTAACGAAAGCACAC | 10451 |
rs113126874 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107829821 | AATGTCAAAAGAGAT[A/C]GCAGATTTGCTCCAT | 10451 |
rs113130656 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107736520 | CAAAGTCTCAGGATA[C/T]AAAATCAATGTGCAA | 10451 |
rs113139085 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107597226 | TTTAAAAATAAAAAA[A/T]AAAAAAAAAAAAACA | 10451 |
rs113146376 | snp | G/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107757437 | GTTTTCTCTCTATAA[G/T]GTGATAAATCTAATA | 10451 |
rs113148790 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | VAV3 | GRCh38.p7 | 1:107913984 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT | 10451 |
rs113161770 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107636417 | TAGAAAGTACAGATG[C/T]TCCTTGACTTATAAT | 10451 |
rs113167670 | in-del | -/CGCGCGCGCACA | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107575008 | GCGTGCGTGCGCGCG[-/CGCGCGCGCACA]CGCGCGCGTGTTTAA | 10451 |
rs113182318 | snp | A/G | 0.030665 | 0.119967 | intron-variant | VAV3 | GRCh38.p7 | 1:107600626 | CTTTTAAGGCTCTCT[A/G]GCACAATTTTTTTTT | 10451 |
rs113192281 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107758846 | TTCTATTCATACTAA[A/T]TTAATTGCAATTCTT | 10451 |
rs113210527 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107825458 | TAGTACCCTCGCGGG[A/G]AAAAAAAAAACTGCC | 10451 |
rs113229550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632566 | AGAAGTATCCATAAC[A/G]CAATTCTGACCCAAG | 10451 |
rs113237675 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107600119 | GTTCTTGGTGTAGAC[A/G]TATTTACTGATTCTT | 10451 |
rs113245034 | snp | A/G | 0.0678174 | 0.1712 | intron-variant | VAV3 | GRCh38.p7 | 1:107918871 | CCACCATGCCCAGCT[A/G]ATTTTTTGTATTTTT | 10451 |
rs113246563 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107870967 | ACGCTCTAGAAATTG[C/T]CTCATTAAAGAAAAA | 10451 |
rs113258345 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107819507 | ACAAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAT | 10451 |
rs113260406 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107745155 | TGCCGTCCTGTTTCA[C/T]ATATGACTAAATGGA | 10451 |
rs113274937 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107960482 | AAAAAAAAAAGAAAA[A/G]AAAAGAAAGGTAAAT | 10451 |
rs113277399 | snp | A/C/T | 0 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570854 | CACATGGAACCCTTC[A/C/T]CCACTTCGGCCTTTG | 10451 |
rs113281224 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | VAV3 | GRCh38.p7 | 1:107734278 | ATTGTAAAGACCAGC[A/G]ATGCTAGGAAGACAC | 10451 |
rs113287996 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107894652 | TAAATGCTTTCCTAA[A/T]AATTCTTAACTTTTA | 10451 |
rs113290400 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107866765 | AAGGTGGAGGCTGCA[C/T]TGAGCCGAGATTGTG | 10451 |
rs113319728 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107955593 | GTGCTCAGCCACACC[C/T]GGGAGAAAAGTCAGG | 10451 |
rs113321447 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107705690 | ACCACAAACTAATAT[A/T]CTTTGTATATTTACT | 10451 |
rs113321656 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107639375 | GTATAACATTATCAA[C/G]AGAATAAAAAAAAAG | 10451 |
rs113325435 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107656972 | TTTTTTTTTTTTTCC[A/G]AGACGATGTCTCGCT | 10451 |
rs113350003 | snp | A/G | 0.283684 | 0.24772 | intron-variant | VAV3 | GRCh38.p7 | 1:107812850 | TTGATAAGGCCGGGC[A/G]CGGTGGCTCACGCCT | 10451 |
rs113350493 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107925211 | GTCAAGATAGAAGTA[A/C]CTTTGAGGCCTGAGG | 10451 |
rs113359352 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | VAV3 | GRCh38.p7 | 1:107815878 | TTCCAGACCCGTGGC[A/G]GGGTGTGGAGGGGGC | 10451 |
rs113379060 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | VAV3 | GRCh38.p7 | 1:107884138 | GAGATGGGGCCCAGT[A/T]TAAAAAAAAAAAAAA | 10451 |
rs113382766 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107830150 | GGTTCTAGAAACTAT[A/G]AGTTTCTCATGCACA | 10451 |
rs113400269 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107957347 | TGTTGAATGACTTCA[A/G]TACCAGTCCTGCTCA | 10451 |
rs113415469 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107612178 | CAGAAATATTTATAT[-/T]GGTCTATATATATAT | 10451 |
rs113419258 | snp | C/T | 0.0565925 | 0.158409 | intron-variant | VAV3 | GRCh38.p7 | 1:107612143 | TTATATATATATATA[C/T]ACACACACACACATA | 10451 |
rs113437283 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107905996 | CAGAAGCAAAGGGCA[C/T]CACCAGAATGTTGAG | 10451 |
rs113450938 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107827303 | AATCCCTCTTCCTTC[C/T]TTATTCTCCAGGTGT | 10451 |
rs113493476 | snp | A/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107859620 | TTTTAAAAATCCCCT[A/C]AATTACAGAAAACTA | 10451 |
rs113502885 | in-del | -/TCTT | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107651706 | CCAGTTCAAGCACTG[-/TCTT]TCTAATTGGCTTTTC | 10451 |
rs113515333 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925915 | ATATATATGTTACAT[A/C]TATAACATACGTATA | 10451 |
rs113520254 | snp | C/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107626542 | CCATGGCCACAGTTT[C/T]AATTCTGCCTTGGCT | 10451 |
rs113531626 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | VAV3 | GRCh38.p7 | 1:107735359 | AAATAACTAAGGTTA[C/G]AGCAGAACTGAAGGA | 10451 |
rs113534423 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107728772 | GCTAATATAATCTGA[C/T]ACAAAAGTGTTTGCA | 10451 |
rs113572358 | snp | C/T | 0.202959 | 0.245534 | intron-variant | VAV3 | GRCh38.p7 | 1:107844482 | CGGAAACATTCACTC[C/T]CCTGGAAAGGGGGCT | 10451 |
rs113586421 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107807626 | ACAGTTTATAACCAG[C/T]ACATAGCCCAGCCCC | 10451 |
rs113605640 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107766215 | TGCGATGCAAAAAAA[G/T]AAGCACCATACTGGG | 10451 |
rs113614324 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107672208 | TGGGAGGCAGAGGTT[G/T]CAGGGAGCCAAGATC | 10451 |
rs113615854 | in-del | -/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107802886 | CTTCCTCTTCAGTTT[-/C]TTTTTTTTTTTGAAG | 10451 |
rs113642010 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107952522 | AAAAAGAAAGACAGG[A/T]GAGAAATACCTTGAG | 10451 |
rs113647497 | in-del | -/C | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107611609 | ACCAAAAAAAAAAAA[-/C]AAACAAACAAACAAA | 10451 |
rs113653928 | in-del | -/A | 0.453453 | 0.145282 | intron-variant | VAV3 | GRCh38.p7 | 1:107958629 | TTAAATTTTACTTAT[-/A]TTTTTTTTATCATTA | 10451 |
rs113654708 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107905223 | TTACCTAGAATTCCT[C/G]CTCCTCCATACTTGC | 10451 |
rs113656559 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107788881 | ATAAGCTACAAAGAT[A/T]ACATGGCAATTTTAA | 10451 |
rs113656676 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107883371 | AAGAATACATCTATA[C/T]TGTCTTTGTATCCCA | 10451 |
rs113672629 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107875034 | TGAGGAATGGAAAAG[A/G]GCTGTTAGCATAAAG | 10451 |
rs113678539 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107640837 | GCATGACCAGACAAA[A/G]GGCTGAGTTATGTGT | 10451 |
rs113681891 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107618402 | TTCAAGATGTGAAAA[G/T]AGAAAACAGTGAAAT | 10451 |
rs113686162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107935630 | GAGTAAGAAACCATC[C/T]GTGACCTGAATAAGT | 10451 |
rs113689566 | snp | A/G | 0.225893 | 0.248835 | intron-variant | VAV3 | GRCh38.p7 | 1:107958749 | CGTCATCTACGTTAG[A/G]TATTTCTCATAATGT | 10451 |
rs113725687 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107936795 | AATTCCCTGCACTTC[C/G]TTTCCTGGTTGGAAT | 10451 |
rs113755983 | snp | A/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107874610 | CCAGCAGAAAAAAAA[A/T]TATCTCTGGAGAAAA | 10451 |
rs113760572 | snp | A/G | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107797726 | TGACCTTTAGGTTGG[A/G]GTAAAAGTTAGTGGA | 10451 |
rs113767198 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107843272 | CTTTGGTGCTTCAGT[G/T]TTTGTATATATAAAA | 10451 |
rs113781465 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107839755 | GGTTCTTTGAAAAGA[C/T]CAATAAAACTGATAA | 10451 |
rs113783822 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107574298 | TATCAAATGCACAGT[C/T]GTGATTTCATTACAG | 10451 |
rs113820145 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107757137 | TATATATGTTTGTGT[A/G]TATATATGTGTGTAT | 10451 |
rs113840468 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107797870 | TAGATTGCTGGGCTT[C/T]ACCACCACAAGATTT | 10451 |
rs113846385 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107851172 | GTGAGACTCCGTCTC[A/C]AAAAAAAAAAAAAAA | 10451 |
rs113847474 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107721735 | TGTTCCTGGGCCTGA[A/G]AAAAAAACGTGATGA | 10451 |
rs113849830 | snp | A/C | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595048 | TTGGAGAAAACTTCC[A/C]TTTTTGAATGAGCAA | 10451 |
rs113866726 | in-del | -/GT | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107843526 | AATGTATGTGTGCGT[-/GT]GTGTGTGTGTGTATA | 10451 |
rs113892002 | in-del | -/T | 0.188797 | 0.242393 | intron-variant | VAV3 | GRCh38.p7 | 1:107802245 | TTTGTTCTAACAGGG[-/T]TTTTTTTTGTGGACT | 10451 |
rs113901036 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107745051 | ACATATCCATAGCTT[C/T]TTAACAAAATTTTGA | 10451 |
rs113915582 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107671490 | TTGAAATGAGAACAT[A/G]TCTACTGCATACTTC | 10451 |
rs113926488 | snp | A/C | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107767013 | CACTGTAAATTTTTT[A/C]AATAAAACTGTCCAA | 10451 |
rs113935115 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107722842 | CCTATTATCCTCTCT[C/T]TTTTTTTTTTTTTGT | 10451 |
rs113959058 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107946286 | TGCAATAATAGCTTG[A/G]CCAGTATCATGAGGT | 10451 |
rs113967885 | snp | A/C | 0.0349115 | 0.127424 | intron-variant | VAV3 | GRCh38.p7 | 1:107614160 | TCGGGGATATACCCA[A/C]GTTTGCATTGTGCTG | 10451 |
rs113986416 | snp | C/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107595740 | ATGGTTTTAGAAATA[C/G]TAGCATCCAAAAAAA | 10451 |
rs113986688 | snp | A/G | 0.5 | 0 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570942 | CCCGGGCCCAGCCCT[A/G]GGCTTCAAGACTCAC | 10451 |
rs113999631 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107931203 | TAGATTATAATAAGA[A/C]ATTGCTCACTTTGTT | 10451 |
rs114002226 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | VAV3 | GRCh38.p7 | 1:107819852 | CATACAAAAATAACT[C/T]ACCTCTGCTCAACAT | 10451 |
rs114006520 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107831283 | TGACATATATCTCTA[C/T]ACAATAATACCAATT | 10451 |
rs114007017 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107859608 | GCAAGCCAAGGCTTT[C/T]AAAAATCCCCTAAAT | 10451 |
rs114031882 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | VAV3 | GRCh38.p7 | 1:107668201 | TGGCATGATCCATAA[C/T]TGTAGCCAGCCTGGC | 10451 |
rs114034458 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897631 | CACCACCTCAGGTGC[A/G]TTCACCCTGCCCATG | 10451 |
rs114037129 | snp | C/T | 0.031825 | 0.122064 | intron-variant | VAV3 | GRCh38.p7 | 1:107663151 | GTTAGTCAGGATTAA[C/T]TGGAAACATCTGAGG | 10451 |
rs114063159 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107864554 | CTTCAGTCAGAGAGA[A/G]GGAGGTTGCAGTGAG | 10451 |
rs114066605 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | VAV3 | GRCh38.p7 | 1:107628239 | TAATCAGCCCTTCAT[C/T]TTTCTATTCAGCTTA | 10451 |
rs114070049 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107633758 | GCCAGCTACCATATA[C/G]GAAGTCTAAGTACCC | 10451 |
rs114072230 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | VAV3 | GRCh38.p7 | 1:107694644 | AGCTCTAGTCTCTAC[A/G]AAGGTGGAACCAAAA | 10451 |
rs114077603 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107891558 | AAAGGGCTCAGTTGG[G/T]GTGGGCACGGTAGCT | 10451 |
rs114081202 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107951264 | CCTCTTCTTGGTCTC[A/G]TCTCTCTCACCCAGC | 10451 |
rs114086021 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107845799 | CAAATATGAAACTAC[A/G]TGAAAAGACCAAACC | 10451 |
rs114087238 | snp | C/T | 0.319856 | 0.240042 | intron-variant | VAV3 | GRCh38.p7 | 1:107811840 | CTCCTCCGAAAACTA[C/T]CTTTGGACTTCTAGT | 10451 |
rs114104184 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107603283 | GTTGGTAATTCTATA[C/T]TAATTACATTGTTTA | 10451 |
rs114115018 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | VAV3 | GRCh38.p7 | 1:107802887 | CTTCCTCTTCAGTTT[C/T]TTTTTTTTTTGAAGA | 10451 |
rs114118243 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590695 | TATCACTTGCCAGTT[A/G]TCCAAAGCAAATACT | 10451 |
rs114150183 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107624858 | TAAAAATGAATAGAC[A/G]TGGACACAATCTTCA | 10451 |
rs114154296 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107619514 | ATAAACACACTACAA[C/T]GCTACCTGAGTGCAA | 10451 |
rs114183014 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | VAV3 | GRCh38.p7 | 1:107597964 | TATCAGTGAGGTGAG[C/T]GAACTTAGGCAAAGT | 10451 |
rs114204012 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107635848 | ATTGGACTCTTGGCC[A/G]GAATTCCTATGTCCG | 10451 |
rs114215165 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107673362 | ATTCTCTTTGTGAAT[A/G]GCTCTCCTGCTCCAA | 10451 |
rs114222383 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107585449 | CCACATCCCTCCAAT[A/G]GTTTCCTGTTTCTTC | 10451 |
rs114222625 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107628781 | GTCTGAAAAGGACTC[C/T]AGTTTTAACTCTACA | 10451 |
rs114223687 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756691 | ATATTCCCCAGTATG[C/T]TCAAAATGTCTGTCT | 10451 |
rs114250070 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107831532 | ACAATTCATATTTAA[A/C]CTTAATAGTTCATCT | 10451 |
rs114250252 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | VAV3 | GRCh38.p7 | 1:107690613 | CTTGTCATTGTCTCC[C/T]GCTTCCTTCCTCTGG | 10451 |
rs114250833 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107913016 | TGGCAATCTCATGTT[G/T]ATACTACCTCTAAAC | 10451 |
rs114251290 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107660874 | AAATTGCAAACGCTA[C/T]GGAAGCACAAACCAA | 10451 |
rs114255205 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107797839 | GCACCAATACCACCT[A/G]GAGGATTTGTTAAAA | 10451 |
rs114256805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592286 | TGATTAGATTCCACT[C/T]ATGCTTTTTGGGGAC | 10451 |
rs114258559 | snp | A/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107959275 | AAAAAATAAATAAAT[A/T]AATTAATTAATTAAT | 10451 |
rs114282423 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107770195 | TTGGCATATGTACAC[A/G]GCTTATACCCTCAGT | 10451 |
rs114292453 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107843127 | ACCTATGAGTCAAAT[G/T]CTCCACATTATGCTC | 10451 |
rs114304386 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107693950 | TTCCAGGCTATGGGT[C/G]TGTAAGTCAGCAACC | 10451 |
rs114308339 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933214 | TTATTGTCTTGTTTT[A/G/T]CTTACAATACTCATA | 10451 |
rs114313102 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | VAV3 | GRCh38.p7 | 1:107608860 | GGATATTATATTTAT[A/G]TATGTATTCTGATAT | 10451 |
rs114331108 | snp | G/T | 0.0263992 | 0.111815 | intron-variant | VAV3 | GRCh38.p7 | 1:107859085 | GGAGTTTTTTTTTTT[G/T]TTTCATTTTTTGGTT | 10451 |
rs114339232 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107610118 | ATACAGAGTGAATCA[C/T]AGTATCTGTCAGATA | 10451 |
rs114356315 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | VAV3 | GRCh38.p7 | 1:107674307 | TGTTTGTTTCAGAAC[C/T]TCTAATTAGCTGCCT | 10451 |
rs114366358 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107685350 | AGATAATACTAGCAC[C/T]GACTTCATAGGTTTT | 10451 |
rs114367251 | snp | C/T | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788617 | ACTGTTTTACCATCC[C/T]CCGGTCCAAATAGCA | 10451 |
rs114370829 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107655995 | AACCCTCATATACTA[C/T]TGGTGGTAATGCTAA | 10451 |
rs114382932 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | VAV3 | GRCh38.p7 | 1:107747926 | AGTTTACATTAACAC[A/G]AGCATTTCTTAAAAC | 10451 |
rs114385986 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107823461 | TGATAAGTGAAGCAA[C/T]GGGAATGGCTGAGAC | 10451 |
rs114393032 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107823216 | GATGACAGACATGAG[A/G]GAATCAAGAATAGTG | 10451 |
rs114406372 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107916223 | AGAAAAAAACTTCCT[A/G]GTAAGTTCAAGTGAC | 10451 |
rs114409218 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107630107 | TCTATAGGTTTAACG[C/T]TAGATATATTTGCAA | 10451 |
rs114409675 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107740532 | AGGTTTATAGTTTTT[C/T]TTGGTGGAGTTAAAA | 10451 |
rs114413162 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107844435 | AGAAGTTTTTTTTCC[A/G]TACCCCAGTGGTTCC | 10451 |
rs114431955 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107605941 | AACCACATAATCTAC[C/T]TGTTAATTTTCTCTG | 10451 |
rs114437726 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107621510 | GCTGTCAATCCCCTA[C/T]GCATGGATGAAATTG | 10451 |
rs114439780 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107695833 | TCAAGTAAGGTAAGG[C/T]CTAAATGTGATGTGC | 10451 |
rs114445374 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107630508 | GTAAGTAATCTATTT[A/G]AAGTCACACTGGTAT | 10451 |
rs114445903 | snp | C/T | 0.030278 | 0.119257 | intron-variant | VAV3 | GRCh38.p7 | 1:107715157 | CTGCCCTTCCTACCA[C/T]ACAAGGCCAACATCC | 10451 |
rs114473079 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107703159 | CCTACTATGAGCAAA[C/T]AAAATGTTAACTGTC | 10451 |
rs114474046 | snp | A/G/T | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107936057 | GGGAGAAAAGTAAAC[A/G/T]TAGGACATTATTACA | 10451 |
rs114475452 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107934020 | TCTCTGGCCAGCTTT[A/G]TTGAATGCAAAACAG | 10451 |
rs114491729 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | VAV3 | GRCh38.p7 | 1:107605287 | AAAGTGATTAGGTCA[C/T]GGGGGCTCTGCCCTC | 10451 |
rs114537793 | snp | G/T | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107939757 | TGGTGAAGTGATCCT[G/T]AGGAGCAGATTAAAA | 10451 |
rs114545787 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107753221 | ATGAAATGGCAAATA[C/T]TGTATGATTTCACTT | 10451 |
rs114549609 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107923458 | AGTGACCTTATAAAA[C/T]AGGCCTGTATTAGTC | 10451 |
rs114559560 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107789105 | GTCAGGCCAGAGGAG[A/G]AACTGTTGATGTGAT | 10451 |
rs114565537 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107595849 | GAGCTGTGTACCAGC[C/T]CTGCTTAAATACTAT | 10451 |
rs114591691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732806 | CTGAATAAAAGGCAG[C/T]AGAAACGTTTGCAGA | 10451 |
rs114596686 | snp | C/T | 0.111928 | 0.208413 | intron-variant | VAV3 | GRCh38.p7 | 1:107840103 | GGAAAATATAATCCA[C/T]AATTTCTTCCAGAAA | 10451 |
rs114603959 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107812255 | ACTCTTGTGCATAGA[C/T]AGATTCATGCACAAT | 10451 |
rs114607222 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107727789 | ACACTCAATCCCTTA[C/T]ACTGAAATTTTATAA | 10451 |
rs114607892 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107783292 | TGAAGGGCAGACTGG[A/G]GTAGAGGACATAGGG | 10451 |
rs114616127 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107595806 | TGAAATAGACCATAA[A/G]CAGATTTGAGATACT | 10451 |
rs114623787 | snp | A/G | 0.0267878 | 0.112589 | intron-variant | VAV3 | GRCh38.p7 | 1:107672623 | TATAAAAATATTTTC[A/G]ATAAATGTAAGATTG | 10451 |
rs114641820 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107671026 | AAAGCATGGCATTAC[A/G]GTTTTTTGAAATGGC | 10451 |
rs114643109 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107707756 | CAGTTCACACTGAAG[C/T]ACAAACTGAGGAGAT | 10451 |
rs114646792 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107707721 | TATGAAAAACCTTGT[C/G]TATGAAACTGTGATC | 10451 |
rs114662183 | snp | A/C | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107796609 | ACACCTGGCTCCTTT[A/C]AAAATATATGAATCT | 10451 |
rs114664609 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107674685 | ACTTAACCTCTCAGA[A/G]CTTTGGTTCCCTCTG | 10451 |
rs114670228 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | VAV3 | GRCh38.p7 | 1:107648842 | ACAGGGAATGAGACT[G/T]GTAGAAAAGAGGCCA | 10451 |
rs114672009 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107626820 | AGTCTTTTGGTGTCC[A/G]GAATCAGTTTTCTTA | 10451 |
rs114672775 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107723882 | ACACATAAAGTGTCC[A/T]GTACTATATCTGACA | 10451 |
rs114674657 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107712406 | ATTTTATGTGTGGCC[C/T]AATACAAATTCTTCT | 10451 |
rs114704098 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107789438 | CCTCAGGACTGCTCA[A/G]AGAAAATCATGAAGC | 10451 |
rs114713712 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107901171 | CTATGTCCCAGGTAT[G/T]GTAGCTGACAATTTA | 10451 |
rs114718387 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107900469 | GAAGTTTCTCTTCCA[A/C]GTGCAAAGTGAAATG | 10451 |
rs114722875 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107647416 | TGACTTCAGCATTCC[A/G]TAAGTGCTGGGCATG | 10451 |
rs114736818 | snp | A/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107885650 | TTTAACCTGCCCTTG[A/T]CTTGTAACAGTACTT | 10451 |
rs114755491 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107951645 | AACACAAACACCATT[A/G]AAAAGTGGGCAAAAA | 10451 |
rs114765441 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | VAV3 | GRCh38.p7 | 1:107726109 | AATAATAATGTGTGA[C/T]AGCCTACCTTCAGGA | 10451 |
rs114771160 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107623342 | TTTTATTTTATCTAT[A/G]ATATTGTTTCTTGAT | 10451 |
rs114773354 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107644178 | CAATACACTGCAAAT[A/G]CCTTTAGTATAGAGA | 10451 |
rs114779991 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | VAV3 | GRCh38.p7 | 1:107646603 | TTTACCTTGTTTTAT[A/C]CCCTACAACAAAAGC | 10451 |
rs114784903 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107668251 | TAAAGTGCACTGATT[C/T]AATGAATGCATTCCT | 10451 |
rs114796721 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107684761 | TGAAAGGAAAATTTT[G/T]CTCTAGATTTGTTGG | 10451 |
rs114798125 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591842 | TAAATACTCAGCACA[C/T]GTTCCTGAAAAACAA | 10451 |
rs114803650 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107693744 | ACTCCTCTGAACTTG[A/G]TACTAAGGGGTGGAC | 10451 |
rs114804912 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107746098 | AATTTGAACCATAGG[C/T]AAAATCAAACTTCAG | 10451 |
rs114805393 | snp | C/T | 0.0551013 | 0.156571 | intron-variant | VAV3 | GRCh38.p7 | 1:107638809 | TAATCAAGACAGCAT[C/T]ACATTGGTACAAAGA | 10451 |
rs114807017 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | VAV3 | GRCh38.p7 | 1:107661293 | AGAGGTGCCACTCTT[A/G]CACGACCCATTATGC | 10451 |
rs114809285 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107731549 | TATTAGGAAATTATA[C/T]TTTAACAGACAAAGA | 10451 |
rs114811680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769166 | CACTAACCATCCCAC[C/T]TCCATCATATCCTCA | 10451 |
rs114815073 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107856826 | AGGATCACTTGAGCA[C/T]AGGAGTTCAAGACCA | 10451 |
rs114817558 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107819396 | TGATATTAGAGACAG[A/G]CACAGTGGCTTGAGG | 10451 |
rs114839899 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107902748 | AGAGGGGAAGGAGAG[C/G]GAAGGCCAGTAGGAT | 10451 |
rs114842756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600233 | AACAAATGAACAGAA[A/G]CAAAATGGAGGGGTA | 10451 |
rs114842840 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | VAV3 | GRCh38.p7 | 1:107642131 | TGGGCAAAATGAGGC[G/T]GAAACCTACTCGACT | 10451 |
rs114845224 | snp | C/G | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590967 | TTCATGCCATTTTCT[C/G]TCTGTAAAACTTCAA | 10451 |
rs114849794 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | VAV3 | GRCh38.p7 | 1:107597028 | CGCAGGTTGGTTTCA[C/T]AGATTCTGCAGAAAT | 10451 |
rs114851897 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107828471 | AGAAAATCAACATGC[A/G]TCTCACTTAAGCCAG | 10451 |
rs114853946 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107928663 | TTGTTTAAGCAGAAT[G/T]AGTGAGCTTGACAGC | 10451 |
rs114860759 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107863668 | TTTCCCTCTACTTAC[A/G]TATATAGATACGTAT | 10451 |
rs114862317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107725100 | AGTGACATCAGGAGT[A/G]AATAAAGGAATCAGA | 10451 |
rs114886877 | snp | G/T | 0.109461 | 0.206758 | intron-variant | VAV3 | GRCh38.p7 | 1:107960343 | TAGTGGCACGTGCCT[G/T]TAGTCCCAGCTACTC | 10451 |
rs114887206 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | VAV3 | GRCh38.p7 | 1:107845671 | CAAGTATCAACAGCC[A/G]AATAGATCAAACAGA | 10451 |
rs114887946 | snp | C/G | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107920310 | TAGATAAAATGCATA[C/G]GAGTTCATCATTACC | 10451 |
rs114889360 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107867755 | GCCAGCTCTAGGCTG[C/G]AAGCTGGCTAATTTG | 10451 |
rs114898280 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107697018 | GCTCATAAAGTCTAG[C/T]TTGCCCAAGACTTCA | 10451 |
rs114900638 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787021 | CACAAAAACACATAT[A/G]AAGTCTGCATCTAAT | 10451 |
rs114916368 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107631191 | TACTGTTTTATTTAC[A/C]GATATATAAAATTTA | 10451 |
rs114927452 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | VAV3 | GRCh38.p7 | 1:107846964 | CCTATAATCAACAGA[A/G]TATATAATCTTCTCA | 10451 |
rs114937543 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | VAV3 | GRCh38.p7 | 1:107809084 | TCAGATCATGCGTCT[A/G]CTCCTTAAGAAGTAT | 10451 |
rs114939073 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107844282 | GAGGGACGGTGCTAT[C/T]CGGCCCAGATACTAT | 10451 |
rs114952345 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107832556 | ATCTGAGTCTTTTAT[A/G]AAATAATTTAAAACA | 10451 |
rs114961254 | snp | C/T | 0.0569829 | 0.158885 | intron-variant | VAV3 | GRCh38.p7 | 1:107633776 | AGTCTAAGTACCCTG[C/T]GATCACCATGCTGTG | 10451 |
rs114985838 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107725803 | CAGGTGTGAGCCACC[A/G]TGCCCAGATGGCAAA | 10451 |
rs114998522 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107616330 | TCATGAGTGAACTAA[C/T]ACAGGAACGGAAAAG | 10451 |
rs115007475 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | VAV3 | GRCh38.p7 | 1:107700417 | CCTAAGAATTAAGTG[C/T]AGCATGCATTAGCTA | 10451 |
rs115010839 | snp | C/T | 0.178785 | 0.239642 | intron-variant | VAV3 | GRCh38.p7 | 1:107612205 | ATATATATAAATAAA[C/T]ATATATGTGTCTATT | 10451 |
rs115024746 | snp | G/T | 0.031825 | 0.122064 | intron-variant | VAV3 | GRCh38.p7 | 1:107640442 | TGAAAGCAGAACAGT[G/T]GTTGCTGAGGGTTGT | 10451 |
rs115027591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913423 | AGTACACTGCTAATC[A/G]CTCACAGCAACAGCA | 10451 |
rs115029579 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107939502 | CAAGTGATCATGAGG[A/G]TAAACAACCAATACT | 10451 |
rs115030352 | snp | A/T | 0.0263992 | 0.111815 | intron-variant | VAV3 | GRCh38.p7 | 1:107663227 | ACTTTCCCTTTGCAG[A/T]TATTCAAATGGAATT | 10451 |
rs115048918 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107898533 | GTTACTTAATACATC[C/T]ATTTACATTATTACC | 10451 |
rs115053951 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107934389 | AGAGCAGAAGATATA[C/T]TTTGCCACTCTTTTT | 10451 |
rs115054703 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | VAV3 | GRCh38.p7 | 1:107958791 | TTGCCCTCCAACCCC[C/T]GACAGGCCCCGGTGT | 10451 |
rs115068682 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107908347 | TGATATCATAGGTGG[C/T]GGCTTCCTATGATTC | 10451 |
rs115069908 | snp | A/G | 0.0225045 | 0.103662 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571601 | TCCCGAGACAGAGTC[A/G]CAGATAAGACTTTAC | 10451 |
rs115078384 | snp | G/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689395 | AGCTCCCAGCCAGAG[G/T]TGAAGGGGAAAACTC | 10451 |
rs115078884 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107889564 | GTTTAGGCAGAAAGA[A/G]CTATATATACTATTA | 10451 |
rs115079942 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | VAV3 | GRCh38.p7 | 1:107653681 | AATATATACATTTAT[C/T]AGTTTAAAATCAAGC | 10451 |
rs115085949 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107680007 | TAGCACACAATAGAA[A/G]ACAAGAAAAAATAAA | 10451 |
rs115106257 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107842291 | AAGGGAAGGGAGTTG[C/T]GAGATGAATAGCTAA | 10451 |
rs115123395 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107904075 | CCACCTTACGTGCTC[C/T]ATCATTTCCTCTTCC | 10451 |
rs115135139 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107607963 | AAGGTTCTATTTTCT[A/G]GGGGAGTTGATCATT | 10451 |
rs115166539 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107782209 | GCTATTCTATTATGT[A/G]TTTTATATAGCAATG | 10451 |
rs115175129 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107824895 | AGAAGAACAGGAACA[C/T]TATTTTAAGAGTAAA | 10451 |
rs115204873 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588335 | GAATAGTGTGTATAC[C/T]GGAATAGTGTGTATC | 10451 |
rs115208536 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107899217 | TTATGAAAGTATCTA[C/T]TTCTTTTACTAAGCA | 10451 |
rs115212816 | snp | A/G | 0.0162398 | 0.0886349 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966850 | CATACTAATCTCTAC[A/G]TACCTTTAGAAGCAA | 10451 |
rs115218937 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107953126 | GAACGGGAAACTTCA[A/C]CGAATCTGGAATTAG | 10451 |
rs115219478 | snp | A/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107847770 | TTCTGAAACTGAGGC[A/T]GTAATTAATAGCTGA | 10451 |
rs115228465 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107855221 | TTGGTGAACAGCATT[C/T]TACTGTCTGTCACAA | 10451 |
rs115254217 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | VAV3 | GRCh38.p7 | 1:107869920 | CCCTTCTTGAGTTAC[C/T]TCACTTAGAATAATA | 10451 |
rs115271345 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107764304 | GCTCATCCCATTCTT[C/T]GGTGACCTAACTCAA | 10451 |
rs115276044 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107753864 | CACACCCGGCCAATG[C/T]TATATATATTTTACC | 10451 |
rs115282216 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107800415 | GATGATGGTTCATTG[C/T]GGTTTTAATTTGCTT | 10451 |
rs115283147 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107599792 | AATTTAATTCCAGGC[A/C]CTATTGTGTTTCACA | 10451 |
rs115284910 | snp | G/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107640932 | GTTGAAAATTTAGGA[G/T]TCAAAAGCCAGCTGA | 10451 |
rs115286930 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107603947 | GTAGTTGATACCACC[A/G]GTGTGGTTGATATTT | 10451 |
rs115289504 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107907673 | CGTTCTCTCTCTCTC[A/T]CACACACACACGCGC | 10451 |
rs115296196 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107718280 | TTGTCCCTGTTCACA[C/G]ATGACATGATTATAT | 10451 |
rs115305181 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107691393 | AACTACTATGGTGGG[C/T]ACTTGGATCTCTAGA | 10451 |
rs115318127 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107931396 | GTACCCTATAAGTAT[A/G]CACAATTATTATATG | 10451 |
rs115321502 | snp | C/T | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107815253 | CCTCCATTGTAGCTA[C/T]GACCTTGACTCAAGA | 10451 |
rs115335824 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107707161 | GGTAAAAGAGTAGAA[A/G]GAAACTATTAGAATT | 10451 |
rs115353870 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107574322 | ATTACAGACCAGCGA[C/T]AATGGCAGAGGAGCT | 10451 |
rs115362812 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107905754 | TTGCTGCTGGCTTCA[A/G]TATTGCTTTCTAAGA | 10451 |
rs115371345 | snp | A/G | 0.0898077 | 0.191933 | intron-variant | VAV3 | GRCh38.p7 | 1:107842862 | GTCTCTCCAATGAGA[A/G]AAATATTAACATAAT | 10451 |
rs115372158 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107803577 | GAGGTTCTTCTTGTG[A/G]TTGATTTCTAGTTTT | 10451 |
rs115378881 | snp | C/T | 0.110167 | 0.207236 | intron-variant | VAV3 | GRCh38.p7 | 1:107927184 | CAACATTTCTAGACA[C/T]ACCCTGGGCCACAAG | 10451 |
rs115385734 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107782707 | ACTGTTTAGTCAATG[C/T]GGTGTTTTTAGAACA | 10451 |
rs115412866 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107939918 | AGGTAGAGAATGTGG[C/T]CCCAGGTGAGGTGCT | 10451 |
rs115432630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107627616 | CAAATACACTTTTTT[C/G]TCCTTTTCAATCTCT | 10451 |
rs115446295 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107921520 | CCAGAACTACACATA[C/T]GGCCTGGACACAGTA | 10451 |
rs115467557 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107735129 | AAATTAAAAACTGAA[C/G]GCAGAAATAAACATG | 10451 |
rs115468375 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107960984 | ATTATACAGTCATTT[A/G]TTTATGGTTCAACTC | 10451 |
rs115485878 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107789411 | CCAAAGATGCTCCAT[A/C]TTTTGTCCCAGCCTC | 10451 |
rs115492773 | snp | C/T | 0.00938699 | 0.0678629 | intron-variant | VAV3 | GRCh38.p7 | 1:107642784 | AAACAAGTTTTAGAA[C/T]TGAGAAAACAATGAT | 10451 |
rs115493790 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | VAV3 | GRCh38.p7 | 1:107819661 | TAAATGGAAAAATTC[A/G]ATTGGGGGAATTTAT | 10451 |
rs115495621 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107784471 | TCAATTATGTGCAGA[C/T]TTTGCTATAGGAAAG | 10451 |
rs115495791 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107806655 | AACAATCCTAACCAC[C/T]AGTTTTCTTCAAATG | 10451 |
rs115507372 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107776750 | TCAGCAGAAGATAAT[C/T]GGCTGCAAGGACCTT | 10451 |
rs115519044 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107899682 | TCATCTAATCTTCAG[G/T]ATTATTTTATGAAAT | 10451 |
rs115519384 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107815759 | AGCAATATCTCCCAA[C/T]TCCCATTATCTTCTT | 10451 |
rs115523652 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107698677 | CAAGGTGTTAGTCCA[G/T]TCTCACACTGCCAGG | 10451 |
rs115526819 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107767130 | GTGTCCTGGTGCTAA[A/G]CTAACAATAATCAGA | 10451 |
rs115527846 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107797774 | TACCAAGTTGATTTT[A/G]TTTTTAACCTTTGGC | 10451 |
rs115534157 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107616376 | TCATTTATAAGTGAA[A/G]GTTAAAATTGAGTAT | 10451 |
rs115556296 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107925470 | ACAAAATATGGTGTA[C/T]ACATACAATGGACTA | 10451 |
rs115560879 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107852491 | CATATATAATCTTAA[C/T]AAAACTGGGGATCAT | 10451 |
rs115561834 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107586321 | GAAGTAGGCTCTCAA[C/T]TAAGATCTGTTGAAT | 10451 |
rs115562851 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107950500 | ACATGACCAGGGGAA[C/T]GACAGAAAGCCAAGA | 10451 |
rs115586588 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107870521 | ATTTGAGTTCCTTGT[A/G]GATTCTTGATATTAG | 10451 |
rs115595486 | snp | G/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107702664 | TTTTATAACGTAAAA[G/T]TTAAAAAATTTTATG | 10451 |
rs115601341 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107633172 | ACCTGTGATAGGAAA[A/C]ATTAGTGAATAAATG | 10451 |
rs115607672 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107677968 | CCTCCAACCAAGAAA[A/G]ATGCGAGCAAGAGGC | 10451 |
rs115625758 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107694096 | AGAAATAAACTTTTA[C/T]ATCTTAAAGCCAATG | 10451 |
rs115639352 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107681349 | GATCCCTTGTTTAAA[C/T]ATTTTGTCTGAAAAT | 10451 |
rs115641476 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107947380 | CATAGACAAGCGAAG[C/T]TATAGAGTTCTAAGA | 10451 |
rs115653101 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107952756 | GCAACACAGGGTCAG[A/G]GATTGAGTTTCATTC | 10451 |
rs115659677 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107835374 | CCCCCAGGTTAGAGC[A/T]GATGGCTCAGGAGTG | 10451 |
rs115666101 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107924314 | AATTGTTATAAATTG[C/T]TTCCACATAAAGAAT | 10451 |
rs115671751 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107876719 | CACCTAAGCAAAATA[C/T]ACACATACCCTAACT | 10451 |
rs115675288 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | VAV3 | GRCh38.p7 | 1:107853186 | CAGCAGTTAAGAGCT[C/T]GTGCTCTGGAATCCG | 10451 |
rs115680633 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107928878 | CCCAATGTAGAGAAA[G/T]ATATCGATATCCAAG | 10451 |
rs115680814 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107872492 | AAAACAACCTATCCA[C/T]ATCCTGTTAAAATGT | 10451 |
rs115682595 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107846607 | CAAAAATAAAGGAGC[A/G]GTTGCAATCCTAGTC | 10451 |
rs115688537 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107863427 | AGCAGGTCATCTCCT[A/G]TCTATGGTCATCTCC | 10451 |
rs115689361 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107831943 | TTGACCAGTCACTGA[C/T]ACAGAACCTAAACCA | 10451 |
rs115698959 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107858166 | CCAGAATTTAAACTA[A/G]AGGAGGAAAATCCAC | 10451 |
rs115707204 | snp | C/T | 0.0228947 | 0.104514 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594748 | TAAACACTAAGGAAT[C/T]GGCTGGGAGTGAACC | 10451 |
rs115722834 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107687929 | CAATAGGATGTGATA[A/C]TCATCATCTTTCTGC | 10451 |
rs115724700 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107618749 | GCCATAAATCAAACT[C/T]AGATGTTCTAACTTC | 10451 |
rs115739088 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107875778 | GCCGGAGCTAGGGTG[A/G]AGGCAGGAAAACCAG | 10451 |
rs115751931 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107597954 | GAAGCTCAAATATCA[A/G]TGAGGTGAGTGAACT | 10451 |
rs115801603 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107838824 | GTGCTGGAGCGTATT[A/G]GCCTAGGTGAACTAA | 10451 |
rs115801896 | snp | A/C | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107847694 | GTAAATTTCTGGAAA[A/C]ATACACCCTCCCAAG | 10451 |
rs115802367 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107801350 | TTTCTGTGAAGAATA[A/T]CACTGATATTTTGAT | 10451 |
rs115805951 | snp | A/G | 0.0592355 | 0.161582 | intron-variant | VAV3 | GRCh38.p7 | 1:107815272 | CTTGACTCAAGACCT[A/G]CTTTCTGTCAATCAG | 10451 |
rs115827016 | snp | A/C | 0.429388 | 0.174127 | intron-variant | VAV3 | GRCh38.p7 | 1:107848700 | accactcctattcaa[A/C]gcaatattggaagtc | 10451 |
rs115829153 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107845968 | CACTAAGATACTCCA[A/C]GAGAAGAGCAACCCC | 10451 |
rs115831168 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107913800 | TTATTATTTTTTTTA[A/G]TTATTATTATTTTGA | 10451 |
rs115833870 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107682770 | TACTCTATTTCTCAT[A/G]TTCCCCTTGGTTTAT | 10451 |
rs115841294 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | VAV3 | GRCh38.p7 | 1:107608681 | GAAGGTGGAGGAGGG[C/T]CCGAGGAGAGTCCCA | 10451 |
rs115854035 | snp | A/T | 0.030665 | 0.119967 | intron-variant | VAV3 | GRCh38.p7 | 1:107673171 | CCACTTCCTTTTTTC[A/T]GAAGAGTATTTAATG | 10451 |
rs115858852 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107722584 | TACTGAATGCCTACT[A/G]TGCTCCAAACAATGT | 10451 |
rs115864369 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107794157 | AATCTCAAAGATCCA[C/T]GTGAGTAGGACATGC | 10451 |
rs115877750 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895536 | AGTTGCCCAATGTCA[C/T]ACAGCCAATAGTTAG | 10451 |
rs115878875 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107866771 | GAGGCTGCATTGAGC[C/T]GAGATTGTGTCACTG | 10451 |
rs115880853 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107819693 | TAGGATTTCATAATG[C/T]CTTTAAAAATATATA | 10451 |
rs115883592 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107903346 | AACACAGCTATAAAA[A/G]ATATCATATTTGCCA | 10451 |
rs115889379 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107664311 | TGGGTATTAAGCTCA[A/G]CTTCCATTACCTATT | 10451 |
rs115892374 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107696847 | CCTGGATATATCTTA[C/T]CCCTTTTCCTGCCCT | 10451 |
rs115904190 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | VAV3 | GRCh38.p7 | 1:107586635 | ATGGTGGGAAATTGA[C/T]AACCATTTACATGAT | 10451 |
rs115922106 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107769503 | TGAGAGTCTGGAGAG[C/G]TGGCCTCAAACCTCT | 10451 |
rs115927022 | snp | A/C | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107633829 | GAGGTCAACGTGCAG[A/C]AAGCCTCTGCTGAGT | 10451 |
rs115964684 | snp | C/G | 0.0026455 | 0.0362733 | intron-variant | VAV3 | GRCh38.p7 | 1:107576456 | AGTTACAAAAGAAAA[C/G]CCACAGAACAAAGAG | 10451 |
rs115972346 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107749963 | ATATTAATGACATCC[A/G]TAGCAGCTTCTACTG | 10451 |
rs115989370 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107857201 | CTGCCAGCATGGCCA[A/G]GATATAAAGCAGGCA | 10451 |
rs115991737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808348 | TTAGGAAAGATAAGG[C/T]AAAAGTAATGAATGT | 10451 |
rs115992435 | snp | C/G | 0.0670745 | 0.170406 | intron-variant | VAV3 | GRCh38.p7 | 1:107835382 | TTAGAGCAGATGGCT[C/G]AGGAGTGACAAGCTG | 10451 |
rs116000209 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107830504 | TATCACAAACAACCC[A/G]CTGGCACAACTACCT | 10451 |
rs116004688 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107862264 | TGTAGTTGTTTGGTG[C/T]TCATACCACTACTGG | 10451 |
rs116004794 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107798437 | AAGAACATGCACCGA[A/G]GCCAGGCGTGGTGGC | 10451 |
rs116008001 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107960752 | AGGAATATTCTTTTT[C/T]CCAAACATTGACATT | 10451 |
rs116011803 | snp | C/T | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966704 | ACTGTTTACACTCAG[C/T]GCTGAACAATAAATC | 10451 |
rs116014421 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107916011 | GAGCATTTAACTCAG[C/T]GTAGAAGTTCAGAGA | 10451 |
rs116030215 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107597413 | AAAACTTGAGTATGT[C/T]GTGGAATGCACTGTA | 10451 |
rs116032170 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107759262 | GTTTCTGCTATAAAC[A/G]AGAACTTAAAGACAG | 10451 |
rs116036754 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | VAV3 | GRCh38.p7 | 1:107648402 | AATATAAAATAACTA[C/T]AAAATTTCATGTGTT | 10451 |
rs116066110 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107807250 | TTGTCAAATATTTCA[C/T]TTAAAATAGATATTT | 10451 |
rs116066240 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107621706 | CATCCCTTTTATGAG[C/T]ATTACAAATGCCAAA | 10451 |
rs116088413 | snp | A/C | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107834758 | CAAACACCAGGGCTG[A/C]TGAGGAAGGAAGCTG | 10451 |
rs116094301 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | VAV3 | GRCh38.p7 | 1:107697403 | AGAAAGGGCACCAAC[A/G]TATAAAACAGAAGGG | 10451 |
rs116095704 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107893947 | GGCTACCTCTGTGCA[A/G]GAACAGTGCATCATG | 10451 |
rs116111431 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107834134 | TTGTTTTCTCATTAT[A/G]CAATTTTGTGTGGCC | 10451 |
rs116116311 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107710221 | CAATTTATGACATCA[C/T]GCTGTCTCATGCTCT | 10451 |
rs116120227 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107842230 | TTTAAACATTTAGTT[A/C]CCAAATTCTAAAATG | 10451 |
rs116131233 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107901323 | AGCAAACTCAGAGAC[A/T]CTGCAGGATATTTTA | 10451 |
rs116139397 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107711316 | TCTTGAGACCCCGAG[C/T]GCAAAGATTTTGGAG | 10451 |
rs116145443 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107871761 | ATATCAAGCCTAAGA[C/T]TCAAAATAAATCTCC | 10451 |
rs116147340 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107824619 | ATCTATATCTGTACT[C/T]CCAGCAAGAGGACAT | 10451 |
rs116152275 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107817609 | AAAGGGAATCAGGGA[A/C]ACCAAACAAGTTAAG | 10451 |
rs116153685 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107652607 | TTTACTTGTTAGTAT[C/T]TATCTCCTCTTGTTT | 10451 |
rs116199639 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107671777 | TTTGTCATATTTTAC[A/C]AAAAAAAACAAAACA | 10451 |
rs116216762 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107596533 | TACCTAATAGCTGTC[C/T]TTGTTACTCAGGCCA | 10451 |
rs116220831 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | VAV3 | GRCh38.p7 | 1:107933399 | AAAATCTGACCATTT[A/C]AAATTCTGAATATAA | 10451 |
rs116221607 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107801883 | ATCCATGAGCATGGA[A/G]TATCTTTCCTTTTTT | 10451 |
rs116229361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107722662 | GAGTATAAGAGGACA[C/T]GCCTGGGCCTGCAGA | 10451 |
rs116246628 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | VAV3 | GRCh38.p7 | 1:107821802 | AGTTAGTAATGTAAC[C/T]GAAATGCAGGTTTCC | 10451 |
rs116252642 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107586945 | AGGGTGTTTTGTGTG[A/G]TATTGAACATAAAGT | 10451 |
rs116253499 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107954056 | TCATGGTTCTATCCA[C/T]TAAATGCCCAAGATT | 10451 |
rs116266226 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107656097 | CACCAATTCCACTAC[C/T]GGGTATATAGCCAAA | 10451 |
rs116269526 | snp | C/T | 0.0973687 | 0.197999 | intron-variant | VAV3 | GRCh38.p7 | 1:107945563 | GCGCGGTGGCTCATG[C/T]CTGTAATTCCAGCAC | 10451 |
rs116273455 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107825269 | GTCTAAAATGACTGT[A/G]TAGCAAGTATCATCA | 10451 |
rs116300994 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107612862 | AGCCAGAAATACCAT[A/G]AGGTTTCTATCTGAA | 10451 |
rs116301802 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | VAV3 | GRCh38.p7 | 1:107932318 | GAAGAGACTATAATT[C/T]AGTGATTTATGTAGC | 10451 |
rs116305113 | snp | G/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107844079 | AACCAGTGAAACCAA[G/T]GCAGAAGGCGGGTGA | 10451 |
rs116310444 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107773260 | TAAAACCAAGTCTGT[C/T]TTAACGCTGAGTGTT | 10451 |
rs116316409 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107875770 | TGAAAGGGGCCGGAG[C/T]TAGGGTGGAGGCAGG | 10451 |
rs116325996 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107887903 | TTTTTGTGACAATTA[A/G]GTAGGAAATATGCAT | 10451 |
rs116336183 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | VAV3 | GRCh38.p7 | 1:107627190 | ACATTCCCTAGGCAG[C/T]GTTTGTTTTCTGTAA | 10451 |
rs116336706 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107666037 | AAGGTCACTATGTTC[A/G]TAAGTAACACCACGT | 10451 |
rs116338861 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107670021 | AGGTTCAGTTTTCTA[C/T]CTTGATTAATACATT | 10451 |
rs116365088 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107710742 | ATATGGATAGTTTAT[C/T]GCCAGGATAGTTAGC | 10451 |
rs116367154 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107795452 | GTATTTGTGATCTAA[C/T]TGTAATACAATGTTT | 10451 |
rs116367739 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107825546 | AGAGAAAAATCTACT[A/G]CTTTCTCATTCCCAT | 10451 |
rs116368067 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107617984 | GGTGGGTGCTGGGGG[C/T]GTGGCAGGTGGTTTC | 10451 |
rs116375712 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107934358 | GACTTGTGATCTGGA[C/T]CAAAACCCTTAGAAC | 10451 |
rs116397393 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107681215 | ATGTGTTGACACTTG[A/G]AGATGTTAAGTAAAT | 10451 |
rs116406212 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788512 | AATTAACACTTTCCC[A/T]CTAAAGAGCAAGCAG | 10451 |
rs116416572 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107927087 | AGTAAAGACGACCTT[G/T]TCTTGCATCTTGGAT | 10451 |
rs116421203 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107673155 | TAAATTATACTAAAA[C/G]CCACTTCCTTTTTTC | 10451 |
rs116421558 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107706075 | TTGATGGCAAAAGAG[A/G]GCAGAAAATTAGACT | 10451 |
rs116462059 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107841267 | CCTCAACAAAGTTCA[C/T]ATTCTGGTGTATTTA | 10451 |
rs116465884 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107853927 | TCTGAACCCCCTGTG[A/T]ATGCCGATTAGGTTG | 10451 |
rs116467287 | snp | A/C | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107846000 | AGACAAATAATTATC[A/C]GATCCCCAAGGCAGA | 10451 |
rs116490505 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107777717 | GGGATCTGATAACAA[A/T]TAATTTGGTAGCAAT | 10451 |
rs116493515 | snp | A/C | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107655462 | ATCTCAGCACATACA[A/C]AAATCAAAGCAAACT | 10451 |
rs116493705 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107690932 | TGTGCCACATAAATA[C/G]CAGCTCCTAGAAGTC | 10451 |
rs116516078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107810833 | GTGAAAAACAGAAAC[A/T]ATACGCGACAGGACC | 10451 |
rs116520493 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895774 | TCATGTGTCCTTGCT[A/C]AAAAATGAATTAGTT | 10451 |
rs116521399 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107794052 | GGGAGGATTAAATCC[A/G]GGCATTATTTAGAAA | 10451 |
rs116521986 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | VAV3 | GRCh38.p7 | 1:107838768 | CTGTGCAGCCCTAAA[A/G]TAAAAAGAATAAAAT | 10451 |
rs116529860 | snp | A/G | 0.202343 | 0.245416 | intron-variant | VAV3 | GRCh38.p7 | 1:107954768 | GGAAAATACCATGGG[A/G]GGGGGGGAAATTCAT | 10451 |
rs116531886 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | VAV3 | GRCh38.p7 | 1:107910204 | TATCCAGGCCTATCT[A/G]ATTCCAAGGCCTTAC | 10451 |
rs116542362 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107666052 | ATAAGTAACACCACG[C/T]GGCCTGAAGAATAGA | 10451 |
rs116552745 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107649615 | CAGCTCCCAGAGCAA[C/G]TGAGCATGTTTTCTT | 10451 |
rs116556955 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107942876 | CTGCTAAATAACAAA[A/G]TCCAACATCTTTTAC | 10451 |
rs116558345 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107949986 | CTGAAAACAGGCTTG[C/T]AAAAATAAGCAGATG | 10451 |
rs116563542 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107621640 | ACTGAATTTCCTTCT[G/T]CTTTACATTACTCTG | 10451 |
rs116570102 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107953820 | CACTCTGAAAACCAT[A/G]GAAGGTGAGTATCAA | 10451 |
rs116572117 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107578062 | ATGAAAGGGTCCTAG[G/T]GATATTTGTGGATAG | 10451 |
rs116576134 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | VAV3 | GRCh38.p7 | 1:107693834 | GACAGACACCAAATA[C/G]TCCATGTGTTTCATT | 10451 |
rs116608227 | snp | A/G | 0.0711525 | 0.174681 | intron-variant | VAV3 | GRCh38.p7 | 1:107840878 | AACCACTGGAAGGAA[A/G]TGAAAACTCTGAGCA | 10451 |
rs116611525 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107596829 | TGATAAAGCACAAAT[A/G]GTACTTGAGACTGTT | 10451 |
rs116617506 | snp | A/G | 0.319856 | 0.240042 | intron-variant | VAV3 | GRCh38.p7 | 1:107811839 | GCTCCTCCGAAAACT[A/G]TCTTTGGACTTCTAG | 10451 |
rs116618008 | snp | A/T | 0.0622301 | 0.165053 | intron-variant | VAV3 | GRCh38.p7 | 1:107845789 | AAGACTCCAACAAAT[A/T]TGAAACTACGTGAAA | 10451 |
rs116635986 | snp | C/T | 0.00752975 | 0.0608948 | intron-variant | VAV3 | GRCh38.p7 | 1:107768538 | AGAAGAAAATAGTAA[C/T]TAAGTATAACTTGTC | 10451 |
rs116638157 | snp | A/T | 0.0295035 | 0.117819 | intron-variant | VAV3 | GRCh38.p7 | 1:107684118 | TAAAAATGAATTCTT[A/T]TTATAGAAAATGAAT | 10451 |
rs116675183 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107752189 | AGAAATAAGTCCTCA[C/T]ATATATGGTCAAATG | 10451 |
rs116690033 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107855953 | AGTGCTTGAGGTCCA[A/C]AGGCTTCACTACCAT | 10451 |
rs116691945 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107781279 | AACTCAGTAAATGTG[A/G]ATTTTTATTATCATG | 10451 |
rs116702715 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107847773 | TGAAACTGAGGCAGT[A/G]ATTAATAGCTGACCA | 10451 |
rs116703098 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107803983 | TGACCCCTTATATTA[C/T]TAATATAGTCACCTT | 10451 |
rs116728257 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107641191 | CTACCACAATTGAAA[C/T]GGTGGTTAGAGACAA | 10451 |
rs116731046 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107707397 | ATAAAACAGGAATAC[C/G]AATAAAACCAAACTC | 10451 |
rs116736433 | snp | A/C | 0.0505692 | 0.150756 | intron-variant | VAV3 | GRCh38.p7 | 1:107748099 | ATAAAACATCCTATT[A/C]CTACCTCTAGTTTAC | 10451 |
rs116765421 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | VAV3 | GRCh38.p7 | 1:107760353 | TATTATAATTTAGTA[C/T]AGTAGAAAGCAATAT | 10451 |
rs116771884 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107915164 | CTTAATCCAATAGGC[C/T]CAAAATGTAGACTAG | 10451 |
rs116784016 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107901125 | TGACAGTATAGCAAG[A/G]GAAAAATAATTTACA | 10451 |
rs116785550 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | VAV3 | GRCh38.p7 | 1:107733475 | TCGAACTCATCTCAA[C/T]GAAGCTAAAAACCTT | 10451 |
rs116804409 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | VAV3 | GRCh38.p7 | 1:107804504 | ATCACAGATCACCCC[A/C]AAAAAGAAACAAGAG | 10451 |
rs116894763 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107785002 | TGATTTTTATTTTGT[C/T]TTAGCTCTTTATTTT | 10451 |
rs116906103 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107751476 | AAAGAAAGACTCAAC[C/T]GGAAGGGTCCAAATT | 10451 |
rs116918605 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | VAV3 | GRCh38.p7 | 1:107925563 | AAGGCATTATGCTAA[A/G]TGAAATAAGCTAGTC | 10451 |
rs116931358 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107940121 | TTACCAGCTGGAGGA[A/G]CTCTTGATGCCTGGG | 10451 |
rs116973853 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107618876 | AGTGATAGCTGAATT[A/C]TGTCATTGGTGATGG | 10451 |
rs117105203 | snp | G/T | 0.0295035 | 0.117819 | intron-variant | VAV3 | GRCh38.p7 | 1:107952004 | TAAACTGTTCTAGTA[G/T]AAAGACACACGTACA | 10451 |
rs117167322 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107704267 | AGTCATTTATTTAGG[A/G]CTTTTAAAGAAATGA | 10451 |
rs117190923 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107615080 | TCAAACTTCAATAAT[C/T]TTTCAAGACTGTAAT | 10451 |
rs117290581 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107739409 | TATAGTTCCCTATCC[C/T]GACTTAACTGCCAAT | 10451 |
rs117304322 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107575288 | GAACTTAAGTGTAAG[A/G]AAAAGAGACAAATGG | 10451 |
rs117309035 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | VAV3 | GRCh38.p7 | 1:107794593 | TGTAGTTGAATTACA[C/T]AGCTATTTTTTGAAA | 10451 |
rs117318448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107960209 | GTGGCAGCTCATGCC[C/T]GTAATCCTAACACTT | 10451 |
rs117360839 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107669671 | TGTTTTCCAGCATGA[A/G]GTTTACATTAGTTTT | 10451 |
rs117367915 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107708141 | GAGATAGGTTGGCAG[A/G]GACCAAGGAAAGAAG | 10451 |
rs117378972 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107901760 | CTTAAAAACAAAACT[A/G]GGCTGGAGAGGGTGG | 10451 |
rs117380881 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107844283 | AGGGACGGTGCTATC[C/T]GGCCCAGATACTATG | 10451 |
rs117405246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107890941 | ACTTTACTCCTATAA[A/G]GCAGATGTGGTGTAG | 10451 |
rs117448288 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107869789 | TGCAGTCTTTTATCC[C/T]TCACCTCCTTTTCAC | 10451 |
rs117500919 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107668207 | GATCCATAATTGTAG[C/T]CAGCCTGGCTAAAAA | 10451 |
rs117505667 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107663063 | TTTAAGAATATATGC[A/G]GTAAATCCACATTCT | 10451 |
rs117513693 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107945777 | CAGTGAATCGAGATC[A/G]CGCCATTACACTCCA | 10451 |
rs117528113 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595181 | TCTACTTTCATTGCA[C/T]GAGCTTAGGCATACA | 10451 |
rs117740082 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | VAV3 | GRCh38.p7 | 1:107740047 | ATCCCACCACTTTGG[A/G]AGGCCAAGATGTGCG | 10451 |
rs117742777 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107681373 | TGAAAATCTCTAAAC[A/C]ATAGCCACATGAGGA | 10451 |
rs117788668 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107912534 | TCTGGCCTGCTGGGA[C/T]AAATGGTAGAGAGAA | 10451 |
rs117881010 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107899345 | TCATCTCATTCACTG[C/T]ATGTCATTTTTGAGC | 10451 |
rs117928741 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107682374 | AAAATATTATGTTCA[C/G]AGTCATATACCCCTA | 10451 |
rs117928799 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107747393 | ATAAGAGCAAAGGCT[C/T]GAGATCAGCTCTGTC | 10451 |
rs117943031 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107930007 | AATTGAACTCATGGA[A/G]ATAGAGAATAGAAGG | 10451 |
rs117946573 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107925636 | GTGTAGTCAAATGCA[C/T]AGGTACAAAAAGTAG | 10451 |
rs117961965 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107638887 | ACATATACATATATA[A/T]GAAGATATATATACA | 10451 |
rs117989464 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107876414 | AGAGAAATGGTCAAG[A/T]GTTTTAAGAAACAGC | 10451 |
rs118042644 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107919391 | GAAATTTCCATGTGG[C/T]TGATAAGTTCTGATG | 10451 |
rs118081304 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107659611 | ATATTTTGTATTTTT[A/T]CATAACCTTCTTGGA | 10451 |
rs118084675 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107793475 | CATGAGAGGAGGGAG[C/T]GTGTCGGCCTTATTC | 10451 |
rs118137364 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107817303 | AGGAGGATTTCCATT[A/G]TCAGAGAAGGGCATT | 10451 |
rs118138494 | snp | G/T | 0.0165278 | 0.0893908 | intron-variant | VAV3 | GRCh38.p7 | 1:107776433 | CAATTTTAGACAGGA[G/T]AGTCAGAGAAGGCCT | 10451 |
rs118139365 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107628073 | TTGGTTCTGAGAAGA[C/T]GTCAGAAAAGGCAAC | 10451 |
rs118165983 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107903161 | TGAGGTAGCAGGATA[A/T]TTAATTTTTTAAAAA | 10451 |
rs118191580 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107810837 | AAAACAGAAACAATA[C/T]GCGACAGGACCAGTT | 10451 |
rs137855899 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | VAV3 | GRCh38.p7 | 1:107757889 | CATACTCTACAAATT[A/C]TATCACAACCACTGT | 10451 |
rs137861624 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107836993 | AGAAAAACTGGTACC[A/C]GTCCTGCTGAAGCTG | 10451 |
rs137868287 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107696010 | CATGCTCCCCCTCTT[A/G]AATTTTTTATTTTAT | 10451 |
rs137884933 | snp | A/G/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107576747 | CATCCTTTTGATGTG[A/G/T]TGCCCAATTCCCACT | 10451 |
rs137890754 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107612744 | TCCTTAAAGTTTATA[C/T]ACAGAATTTGAGGTT | 10451 |
rs137900647 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107681750 | GTTCTGCCTCCCGGG[C/T]TCACGCCATTCTCCT | 10451 |
rs137931130 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107723184 | AAAACTGCTGTAGAA[C/T]AAATTTATCCATGAA | 10451 |
rs137931235 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107761118 | TTCTTGGCCGGGCGC[A/G]GTGGCTCACGCCTGT | 10451 |
rs137950595 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107727601 | ATTTAAAATTAATAT[G/T]TGACTATTTCCCAAT | 10451 |
rs137959801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107935081 | TTGGCAAACATTCAT[A/G]TCAGCCAATTTGCCA | 10451 |
rs137960924 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107652326 | GGCATGAATAATCCA[C/T]CCCTTGTTTAGCAAA | 10451 |
rs137970683 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107938974 | GCAAACGCTGAGCTA[C/T]ATCCAATCCAGCTGA | 10451 |
rs137985643 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107871797 | CCCAAACAGAGGGAG[A/T]GCTTGGACAAAGTTT | 10451 |
rs137998136 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107607080 | CTGCCTCAGCCTCCC[A/G]AGTAGCTAGGATTAC | 10451 |
rs138000883 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107791238 | ATTGCCAATAGCCTT[A/G]TGTGCCCCATTAAAC | 10451 |
rs138016745 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107692388 | ATTATTAATGTACCA[C/T]TAAACTGACCCAAAT | 10451 |
rs138020928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107753016 | ACAATAATAATATAA[C/T]AGTATTATTCACAAT | 10451 |
rs138030837 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107825931 | TATTGTAAATCCCTA[C/T]CTATACAGTTAGGTT | 10451 |
rs138032704 | snp | A/G | 0.0433465 | 0.140692 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570661 | TCCATTGGCTTCTCT[A/G]GGATCCTTCGCATTA | 10451 |
rs138036694 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107641955 | ATAAAAAATATTTTC[C/T]GCATATCATGTAAAG | 10451 |
rs138038228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107611415 | TTCTAATCATTCAAA[C/T]AGTTTCTTACATAAC | 10451 |
rs138049298 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107925401 | GAGCAGCATTACTCA[C/T]GATGGCCAAAAGATT | 10451 |
rs138055540 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860168 | CTCTATCACCCAGGC[A/G]AGAATGCAGTGGCAT | 10451 |
rs138068618 | snp | A/C | 0.000977605 | 0.0220873 | intron-variant | VAV3 | GRCh38.p7 | 1:107779514 | AAAGAGGAAAATACT[A/C]ATTAGATATGTAGTT | 10451 |
rs138070806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831022 | TAACCACAAATACTT[C/T]TACAGGTTGAGTATC | 10451 |
rs138075346 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107815100 | AATTACAATCTATAC[A/G]TAGATGCTGCAGTAT | 10451 |
rs138083468 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964013 | TAGTGAAACTTCTCA[A/T]TTCCTGTCGCTGCTG | 10451 |
rs138088788 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107715955 | TGATCTAGAAGCATA[C/T]GGAGATGGAGATGGT | 10451 |
rs138118714 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107885331 | ATGATATGCTAATGG[A/C]AGACTAATGCTAATG | 10451 |
rs138127533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107746710 | GTTGGTCAGTATTAT[A/G]TAACAGAAGCGAGTG | 10451 |
rs138128667 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107887176 | ACCCACCAATGCTCC[A/G]TCCAACCTGGCAGCG | 10451 |
rs138144865 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107893583 | CAGCAGGCAAAAAAA[G/T]CTTCCGGAGGGAAAC | 10451 |
rs138148334 | snp | C/G/T | 0.284711 | 0.270583 | intron-variant | VAV3 | GRCh38.p7 | 1:107850271 | AAAGACACATGCCCA[C/G/T]GTATGTTTATTGCAG | 10451 |
rs138152504 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107714940 | AATTTTAAATATACA[G/T]CTGTCACTGCATTTC | 10451 |
rs138155339 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107842962 | GAGGAACTTTATCTA[C/T]GATGAGAGCAGAAGC | 10451 |
rs138170759 | snp | A/G | 0.00270032 | 0.0366452 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964797 | CCTGAGCCGAGTCCC[A/G]GGTCACCCGGTGGTT | 10451 |
rs138171453 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107774886 | CAGCAAACTCAAAAC[C/T]AAGCATGTCTAGGGA | 10451 |
rs138179769 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107854330 | ATAAAATAAAATAAA[A/G]TTATGCTAGGTTAAC | 10451 |
rs138185433 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590163 | TGACAAAAGTAGCCT[C/T]TGTCAATCTTTGAAG | 10451 |
rs138200097 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107784035 | ACTGCACTCCAGCCT[G/T]GGTGACAGAGCAAGA | 10451 |
rs138209497 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107882288 | TGTTGAAGAAAGAAG[C/T]TCTCAGCATCTCAGA | 10451 |
rs138215394 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107809034 | TTCACAAGGCTGAGC[A/G]CAACCTGCCCAAAAG | 10451 |
rs138224836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107670112 | AGAAAACTGAGGCTT[A/G]TTAAATTGTCCAAAG | 10451 |
rs138228452 | snp | A/G | 1.68298e-05 | 0.00290079 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107705007 | GACTCGAGTGAAGGT[A/G]TGCATCTTGAAGTCG | 10451 |
rs138235809 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107703544 | ACAGAGAATGGCACA[C/G]AGGGTCCTTTTAAAA | 10451 |
rs138238020 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107766842 | AGAGGAGAGGGAGGA[G/T]AAGAGAAGGAGACAG | 10451 |
rs138238287 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107679787 | TGTTCTTGAAAAAGG[C/T]CTAGCACCTCCGTGT | 10451 |
rs138273611 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107598984 | TTTTGTTATAGGTAA[C/T]ATGAATTTTATGATT | 10451 |
rs138278003 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107683344 | GATTTACACGTTAGA[C/T]CATGACCTCCTGGTC | 10451 |
rs138305160 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107952724 | ATGAAGTAAAACCCG[A/T]ACTGTATAGACTAAA | 10451 |
rs138305193 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107584731 | GATTATTGTAAAAAA[C/T]AAACTACTACTTAGT | 10451 |
rs138306870 | snp | C/T | 0.259397 | 0.249823 | intron-variant | VAV3 | GRCh38.p7 | 1:107736438 | TGTTTGCAGATGACA[C/T]GATTGTATATTTAGA | 10451 |
rs138310027 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107777914 | CTTGGGGTGAATAGA[A/G]TGTTTTCTTTGTTCC | 10451 |
rs138325007 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107880212 | TGGAATAACTGATAC[A/G]TGAGGTAAGAAAGGA | 10451 |
rs138328024 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107868747 | ATTGCTTGGAACTTC[A/G]GTAATAAAGATTAAC | 10451 |
rs138334746 | snp | G/T | 0.00314804 | 0.0395488 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107609935 | TTAATACTTACCAGG[G/T]TTGGCAAGAATAATC | 10451 |
rs138335150 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107939310 | ATTTTCTTGCCTTTA[C/T]ACAGATGGTCCTAGG | 10451 |
rs138337182 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | VAV3 | GRCh38.p7 | 1:107841273 | CAAAGTTCATATTCT[A/G]GTGTATTTAGGGGAA | 10451 |
rs138340546 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107954996 | AATTAGATGAGATAA[C/T]GCATGGAAAGCTTTA | 10451 |
rs138348214 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107668498 | GTAAAACCTCTAGTA[C/T]ATCAACAAATATCAC | 10451 |
rs138351701 | snp | C/G | 0.0520825 | 0.152737 | intron-variant | VAV3 | GRCh38.p7 | 1:107738140 | TGTTCTCACTCATAG[C/G]TGGGAATTGAACAAT | 10451 |
rs138363543 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107653989 | CACGAAAACACTACA[G/T]GCTAGCACAGTGCCT | 10451 |
rs138369468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107673992 | AAAAGTGTATGCTGC[C/T]TCATTTTTAAATAAT | 10451 |
rs138384229 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107607512 | CCCCAGTCTCTGCTA[G/T]GCTTGATCTTTCCAA | 10451 |
rs138402595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624723 | AACACTAAATGCTCA[C/T]GGCAGCATGAGATAT | 10451 |
rs138410421 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107844511 | CTGAAGCCAGGAAGC[C/T]GAGTGGTCTTGCTCA | 10451 |
rs138435741 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107628776 | CACAAGTCTGAAAAG[C/G]ACTCTAGTTTTAACT | 10451 |
rs138444389 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107864362 | CGTGGTGGCTCATGC[C/T]TATAATCCAAGCACT | 10451 |
rs138444804 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107849334 | CTTCAAACTATACTA[C/T]AAGGCTACAGTAACC | 10451 |
rs138444886 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107796370 | CAAACAGCGAACCAG[G/T]CTCATTGGTTATTTT | 10451 |
rs138457766 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107899074 | ATATGATGAAGATGA[C/T]GAAAGTATGTATGTG | 10451 |
rs138476893 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107836123 | ATTAGACAGATCATC[A/G]AGGCAGAAACCTAAC | 10451 |
rs138477659 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107934144 | ATTCTTATTATCTTG[C/G]AATTATAAGAACTCT | 10451 |
rs138491359 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107903594 | AAAGACAGTAATAAG[A/G]GCATTCACCTAAGAT | 10451 |
rs138499021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911862 | GTCCTTTAGATTCCT[C/T]TGTCCATCAATTACA | 10451 |
rs138528704 | in-del | -/ACTCAAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107763021 | AGAAAAAGACAAAAA[-/ACTCAAC]AAGAACAAAAATAAC | 10451 |
rs138533817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107692682 | TCTCTCAGTTTTAAA[C/T]CACTAGGATACCACA | 10451 |
rs138537590 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | VAV3 | GRCh38.p7 | 1:107800790 | TCTTCACTTTGTTGA[C/T]TGTTATCTTTGCTGT | 10451 |
rs138559051 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787869 | CGTCTCTGCCTTCTT[A/G]ACCTCAACACTCTGC | 10451 |
rs138565406 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107819950 | TTTTATCCAAAGACA[A/G]GCAGTAACAAATGCT | 10451 |
rs138568235 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107722607 | AACAATGTCCAATAA[A/G]AATACAAATGGAATT | 10451 |
rs138572112 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107700392 | GTTTGCTGCACCTAT[A/C]AACGCATCACCTAAG | 10451 |
rs138582628 | in-del | -/AA | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107638114 | GTCATACTTAATGGT[-/AA]GAGACTTAATGTTTT | 10451 |
rs138583042 | snp | A/T | 0.029116 | 0.117091 | intron-variant | VAV3 | GRCh38.p7 | 1:107753420 | AATTTGAAAATAATT[A/T]GAATGGCAAATTAAT | 10451 |
rs138585083 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107795639 | TACTTGATAACAACC[G/T]GAATCAAGAGGGAAA | 10451 |
rs138587338 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107617147 | ATTTAGACATTTGAT[C/T]GAAAAATTTGTGGAC | 10451 |
rs138589006 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107684757 | TGAATGAAAGGAAAA[C/T]TTTGCTCTAGATTTG | 10451 |
rs138600449 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107600623 | AAACTTTTAAGGCTC[C/T]CTGGCACAATTTTTT | 10451 |
rs138606986 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107887541 | TGTCCTTCTATCTCC[A/G]TGATAAATGTCCCCA | 10451 |
rs138611523 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107757642 | AATCACACTTTTTAC[A/T]CATTTATTATTCTTG | 10451 |
rs138619788 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107702775 | AAAACAATAAAAATA[C/T]TAAATAAGCCCACGT | 10451 |
rs138624578 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107695432 | GACTTAGGAGGAGAG[C/T]TAAGAAGAACAGGAA | 10451 |
rs138634593 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107620853 | CTTTCTTCCTTTGTA[A/G]AAACAGGTGTTCCAC | 10451 |
rs138644094 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107775263 | TAAAAATTTATAGGT[G/T]TAAGTCACCACTGGT | 10451 |
rs138655991 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107647141 | GCGATTGCTACAACA[C/T]AGATTAGTATCTATT | 10451 |
rs138670630 | in-del | -/TTA | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107709429 | AGATAAGAGACATTT[-/TTA]TTAAGCCAAAAAAAA | 10451 |
rs138683914 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107891753 | TTGAGGCAGGAGAAT[C/T]GCTTGAACCCGGGAG | 10451 |
rs138690815 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107651253 | ATTTTGTTGGAGCAG[C/G]CTAAACAGACTAAAA | 10451 |
rs138716926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893888 | TCATGAATATCCCCA[A/C]AAGATCCCAAAATAG | 10451 |
rs138724574 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107678521 | TGAAAACACTCTGTT[A/G]TTATTTTTCTCAATG | 10451 |
rs138727424 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107741177 | AATATTAACAAAGTG[A/T]ATCTTTTAAATTTTC | 10451 |
rs138735680 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963401 | ATGCATGTTTATGGG[G/T]GTATAAAATAATTTA | 10451 |
rs138739717 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107885176 | TGCCTTGCCCCAGAA[A/G]GAGGGGAGCTGGGGT | 10451 |
rs138746894 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107864447 | GGCAACATGGCAAAA[A/C]CCTGTCTCTACAAAA | 10451 |
rs138748534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107854882 | ATGCTAAAGTTTAAT[C/T]TCATTCACATAATAA | 10451 |
rs138760168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950297 | ATGTAACTTGTAAAG[C/T]TTGGCACAGTTGCTA | 10451 |
rs138769886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107859662 | AAACTCAAAGAGGAG[A/C]AGTATAAATTCAATA | 10451 |
rs138770008 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107924943 | CCCAAAAGATATGTA[C/T]GCATTCAGCAAAAGA | 10451 |
rs138777695 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107742344 | CGCATGTGAACAACA[A/G]GGACAAGATCCCTGC | 10451 |
rs138784544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107849728 | AATTGACACATGGGA[C/T]CTAATTAAAGATCTT | 10451 |
rs138787549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868340 | CAGGTGTTGATTAAC[A/G]TGTATGCACTAGATA | 10451 |
rs138789168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814452 | TTGTGTCTTCCTTTG[A/T]GAAATGTTTATTCAT | 10451 |
rs138801343 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | VAV3 | GRCh38.p7 | 1:107771063 | ACAAATACTATAGAA[A/G]TAACTGCAAAAACAA | 10451 |
rs138817273 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107708867 | AATCATGACCAATTT[C/T]GGTCAATTCAAGCTT | 10451 |
rs138836065 | in-del | -/CCTC | 0.236434 | 0.249632 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895867 | CAATATGAAAATTCT[-/CCTC]TTATTGTTACTATGC | 10451 |
rs138849029 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107629776 | CATTCAATAGCATCA[G/T]AAATTACTGTTGTTA | 10451 |
rs138853204 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107664734 | ATAGCAATGTTGTCA[C/T]GGGAGAGGGACCCAC | 10451 |
rs138864739 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107818499 | GAAAGGAAGGGAAAG[G/T]AGGGAGGAACACATA | 10451 |
rs138880547 | in-del | -/GCCTGGGGCTTGCACCCTCTGAAGCAACA | 0.497855 | 0.0326773 | intron-variant | VAV3 | GRCh38.p7 | 1:107701314 | CCCTCTGAAGCAAAG[lengthTooLong]GCCTGAGCTGTACGT | 10451 |
rs138893268 | in-del | -/AGTTTGT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107598634 | AAAAGACCATGTAGA[-/AGTTTGT]AGTTTGTATCTCCAA | 10451 |
rs138896569 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107843769 | CGGAAAAATGCATTT[C/T]TGGGGGAGTCTTTTG | 10451 |
rs138911780 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107711745 | GTCTTGCTCTGTCGC[C/T]CAGGCTGGAGTGCAG | 10451 |
rs138921838 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107623803 | TATGATCCTTAACTT[C/T]TGTCCAATGTATAAA | 10451 |
rs138927064 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107824959 | TAGGGTCCCATTATT[C/T]GAAATGAGGTGATCC | 10451 |
rs138930981 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107844286 | GACGGTGCTATCCGG[C/T]CCAGATACTATGTTT | 10451 |
rs138939858 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107907654 | TCTTGCTCTCGTGTG[C/T]GTGCGTTCTCTCTCT | 10451 |
rs138946199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107585290 | GTTCCAGGCCACTAT[C/T]ATCTCTTACCTTGAT | 10451 |
rs138950313 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107669706 | TTTTTTTTAGATTGT[C/T]ATCCCTTTCATCTAT | 10451 |
rs138951751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795927 | ATTCCTGATTCCCAT[A/G]CTGATCTCACCTCAT | 10451 |
rs138954913 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107894161 | GGACACTGTTTACTC[A/G]GGCAAGAATTTTCAT | 10451 |
rs138955500 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107715144 | CAAAGAACTATACCT[G/T]CCCTTCCTACCATAC | 10451 |
rs138962162 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107730409 | CCTTTACTTCTAAAA[A/G]CAGAACTTAAACTCT | 10451 |
rs138969246 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107635939 | TGCCTCAGTTCACTC[A/G]TCTATAAATTGAGGA | 10451 |
rs138973333 | in-del | -/AAAC | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966504 | AGACTCTGTCTCAAA[-/AAAC]AAACAAACAAACAAA | 10451 |
rs138981551 | in-del | -/TTCCCCA | 0.497749 | 0.0334707 | intron-variant | VAV3 | GRCh38.p7 | 1:107701530 | TGCCCTGGAGACATT[-/TTCCCCA]TTGTCTTGGCAATTA | 10451 |
rs138981948 | snp | C/T | 1.71752e-05 | 0.00293041 | synonymous-codon, intron-variant, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107688396 | CTCTGGTAGTTTGAG[C/T]GTCCCTTGTTCTGAA | 10451 |
rs138983408 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107707465 | GACCCATATTTGGTG[C/T]TCAATCAATGTTGGC | 10451 |
rs138988479 | in-del | -/TGAG | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107915505 | AATCCTATGTGAAAC[-/TGAG]TAAGTTACTTGATCT | 10451 |
rs138992974 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | VAV3 | GRCh38.p7 | 1:107944945 | GAAGTTAAGAGTGTA[A/G]TATGAAATAGCTTGC | 10451 |
rs138993498 | snp | A/C/G | 9.22433e-05 | 0.00679066 | intron-variant | VAV3 | GRCh38.p7 | 1:107785442 | CAAAAGGAATTCCGA[A/C/G]GGAAAGGGTACTTAC | 10451 |
rs138994948 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107719269 | ATCAGAGTGAACAGG[C/T]AACCTACAGAATGGG | 10451 |
rs139004980 | in-del | -/TAAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822669 | AAAAAAATAAATAAA[-/TAAA]TAAATAAATAAATAA | 10451 |
rs139010754 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590735 | TACTTGTACTAATTT[G/T]ATTTCAAATCCTTTA | 10451 |
rs139010867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872836 | AACCTCTTAACGTTG[C/T]TACAATTTTACAAAT | 10451 |
rs139017668 | snp | A/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107876755 | GGCACATATTTTTTT[A/T]AAAATATACATGTGA | 10451 |
rs139021041 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107641680 | AACTCCAGGTATTAC[A/T]GTGGGTAGGTAAAAA | 10451 |
rs139027827 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107833011 | TACATGATTTTTTTC[A/G]CAACTAGAAAATCAT | 10451 |
rs139054658 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107643413 | TCTTTGAATGTGCAA[G/T]GAAGGCCTCAGTTCA | 10451 |
rs139061647 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592980 | TGAAGTTTCTAGAGG[A/T]AGCCCAAGAGCTCCC | 10451 |
rs139062285 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107864496 | GCTGTGGTGGCATGC[A/C]CCTGTAGTCCCAGCT | 10451 |
rs139063935 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107909640 | TATGGTGTAATCTTA[G/T]TTTTCTTGCTGCATT | 10451 |
rs139065569 | snp | C/T | 0.00014958 | 0.00864683 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107760839 | ACCACAAGCAAGTCT[C/T]GAAGAGTAAATTTCC | 10451 |
rs139073388 | snp | C/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107851155 | CCAGCTTGGGAGAAA[C/G]AGTGAGACTCCGTCT | 10451 |
rs139088405 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107680929 | GTTTCATTAGCATAT[C/G]AGCAGGAGGAATTTA | 10451 |
rs139090386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107743137 | GAAAGATGGGTGGGA[C/T]AAAACCAGTCAGGGC | 10451 |
rs139097024 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107595972 | TTAGCATATCTTTTA[C/T]GTTTCTGCTGGATTT | 10451 |
rs139101725 | snp | A/T | 0.0539704 | 0.155153 | intron-variant | VAV3 | GRCh38.p7 | 1:107735523 | AAAATGATAAAGGGG[A/T]TATCACCACCGATCC | 10451 |
rs139108761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632126 | CACCTTATTTTGTAG[C/T]TACGTTTAATAATAC | 10451 |
rs139129491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912715 | CTCCTCCAGGTCAGG[C/G]ACTAGATACCTGCAT | 10451 |
rs139156424 | snp | A/G | 1.64985e-05 | 0.0028721 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107777245 | CTCTATTAAATCAGG[A/G]AGGCCTTTGTAGATG | 10451 |
rs139158361 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107801602 | ACCACTCATAGACTA[C/T]TGAGTGTTCAAATTG | 10451 |
rs139168819 | in-del | -/TTTAT | 0.0599851 | 0.162463 | intron-variant | VAV3 | GRCh38.p7 | 1:107878034 | TTTTTTTCCAGTTTA[-/TTTAT]TTTATTTTTTTGAAT | 10451 |
rs139173316 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107853980 | TTTTTTTTTCTAAGT[G/T]GGGATATTGCTAAGA | 10451 |
rs139176082 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107910166 | AAGATTACACAGCTA[C/G]TAAGAGATATCAGTG | 10451 |
rs139195363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739182 | GAAGTATCAAATACA[C/T]ATTAAACATAACCAG | 10451 |
rs139198196 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107761611 | CAGTTCCCTCAACTA[C/T]GATGTGCTTTGTCCA | 10451 |
rs139214910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107881357 | ACCTCAGAATTATAA[C/T]TGTACCTCTCTCTGC | 10451 |
rs139215279 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107708996 | TTGTTTCTCTAAAGA[A/C]TCCTAATATAGACAC | 10451 |
rs139223866 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107625357 | CTGCAACCTCCGCCT[C/T]CCGGGCTCAAGTAAT | 10451 |
rs139226534 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107725409 | GTGGAAATATGCAGC[C/T]GAAAGTAAAGAGAGT | 10451 |
rs139229542 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107698023 | CTTAGGGGCTGGCCT[A/G]CCTGGATTTGAATCT | 10451 |
rs139243056 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107601693 | GTTTACTGTTAGCAA[C/T]GCATACATGATGATA | 10451 |
rs139244575 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107581000 | GTAACAGTGACATTT[A/G]AATGGGAACGTTGAG | 10451 |
rs139245507 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896763 | ATGGCTACAGGAATG[C/T]CATGTTCCGTTCCAT | 10451 |
rs139255608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107702947 | GAATAAACAAAAGCT[C/T]AGAATATTTAAGTAA | 10451 |
rs139278281 | in-del | -/TATATATGT | 0.304937 | 0.243889 | intron-variant | VAV3 | GRCh38.p7 | 1:107925900 | ATATAACATATATGA[-/TATATATGT]TATATATGTTACATA | 10451 |
rs139302493 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571356 | AACAAAGTATTAAAC[A/G]TGGACAAAGATGTAA | 10451 |
rs139317930 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107873871 | ACCAGGGCCTTCCCC[C/G]ACCCCAGGTAGAGTG | 10451 |
rs139333841 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107882981 | TAGCTGTAATCTTGT[C/G]ATCAGTTCACTAAAC | 10451 |
rs139337396 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107754115 | ACAATGTAAAGTTTA[C/T]GGGCAGTTATTAGCT | 10451 |
rs139343102 | snp | C/T | 0.000581001 | 0.0170342 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107766452 | CAAAAGTTACCTTTC[C/T]TTGTAGTTAATAAAA | 10451 |
rs139348525 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107960950 | TAAATTGTATGTAAA[A/T]ATATAAATATATAAA | 10451 |
rs139351899 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572134 | ATTTAGGCTCCTCAC[A/G]AAAAAGAGTGATGGC | 10451 |
rs139363500 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107644736 | GATGACATTTCACCA[C/T]CCAAATATATATTAG | 10451 |
rs139372668 | in-del | -/G | 0.0232847 | 0.105357 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593130 | GAGACAGCCTACAAT[-/G]GGCCCCTAACTTTAA | 10451 |
rs139379733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107928600 | GTCGAAATTATGAAG[C/T]TTAAAAATGCAATGA | 10451 |
rs139384250 | snp | A/G | 0.00288365 | 0.0378617 | intron-variant | VAV3 | GRCh38.p7 | 1:107768407 | AGATTTTATTGAAGT[A/G]CACCACAATTTTAGC | 10451 |
rs139396262 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107846374 | GACCATCAACACTGT[A/G]AAGAAACTGCATAAT | 10451 |
rs139401468 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107658262 | CTTCATCCATGTCCC[C/T]ACAAAGGACATGAAC | 10451 |
rs139424305 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107771533 | GCTGGGATTACAAGC[A/G]CGAGCTACCGCGCCC | 10451 |
rs139424396 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107731732 | AGGCATCCAAGCACA[C/G]CATATACTTGGAAAG | 10451 |
rs139437231 | in-del | -/TTTG | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107824351 | GAAGCAAGGAACTTC[-/TTTG]TTTGTTTGTTTGTTT | 10451 |
rs139438636 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107661186 | AAAAGTTTCTGCCCC[A/C]GGGTAGACACTTTCC | 10451 |
rs139439371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107749401 | ATTAATGTATTATCA[C/T]ACTTTTCCTTAATGT | 10451 |
rs139462251 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107734714 | GATTCATAAAGCAAG[A/T]CTTTAGAGACCTACA | 10451 |
rs139476510 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107614223 | GCTAGAAATGAAGTT[G/T]ACCCATTTATGAACC | 10451 |
rs139478383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107665472 | CTCCTTGGTACAGCA[C/T]TGCTAAACACTTTTG | 10451 |
rs139483020 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107826649 | AAGTCAAGGGCTATT[C/G]CAGGCACTTAAGCTT | 10451 |
rs139493342 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107883264 | TGCTCTGCAGCACCC[A/G]GCTCACATCTGTTAT | 10451 |
rs139498906 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107815793 | CCACATATATGCACA[A/C]ATTTTTTTGCCTAAC | 10451 |
rs139511776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107716924 | TTTCACAGCCTGTTA[C/T]TGGTATACTCAGGGA | 10451 |
rs139518329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618112 | TGAGAATCTAATGCC[A/G]CCACTGATTTGACAG | 10451 |
rs139519568 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107888093 | TAAAAAGAAAGGATT[A/G]ATGGTTACTTTATAA | 10451 |
rs139525804 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | VAV3 | GRCh38.p7 | 1:107768702 | ATAAAAACATAAATA[C/T]GAGCTAATATTAATA | 10451 |
rs139536723 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773156 | GTGTGCATTATTATT[A/T]AATCCATTAAAGAGA | 10451 |
rs139538937 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107820522 | AAAAATAGAGTTAGA[G/T]AGAATGAATAAGATC | 10451 |
rs139541501 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591360 | TATAATTCAAGTATC[C/T]AGCACAAGGCCTAGC | 10451 |
rs139557468 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107709809 | TTTGTCTCCCCTTCT[A/G]CCATGACTATAAGTT | 10451 |
rs139575806 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107775520 | GAGGTGGAGGTTGCA[A/G]TGAGCTGAGATCGTG | 10451 |
rs139592015 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107712831 | TGAAACTGCAGCTAT[C/G]ACAAGTGCTACAAAG | 10451 |
rs139601644 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107881100 | AACTACTATGTTATA[C/T]TAACTCCATTTTTGC | 10451 |
rs139615788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107712307 | GCCCAACACAAATCC[A/G]TAAACTTTCTTGAAA | 10451 |
rs139623540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842361 | GCCCAGGAGTGAACA[G/T]CTGACTCAAGGTGAG | 10451 |
rs139625315 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107828726 | ACCCATATGATTACA[C/T]TGGGCCCACCCAGAT | 10451 |
rs139631733 | snp | A/C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107892330 | ACTGAGTGCCCATTA[A/C/T]GTACTAGGTACCACT | 10451 |
rs139632059 | snp | A/G | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107945737 | TGAGGCGGGAGAATC[A/G]CTTGAACCTGGGAGG | 10451 |
rs139634363 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107762316 | GGCACATGGAATGAT[A/G]TATTATGAGGAGCTC | 10451 |
rs139637599 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107672157 | ACCTGCAATCTCAGC[C/T]ACTTGGGTGGCTGAG | 10451 |
rs139648277 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107671624 | AAATTAAGATGAGGA[C/G]GATTTGTAAAATAAA | 10451 |
rs139651636 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107621475 | ACGTTGGTAATTCAT[A/T]AATACTAATGGGTGG | 10451 |
rs139656217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586868 | ACTAATCACAGTAAA[C/T]AGCTATAGTACATCA | 10451 |
rs139671685 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107674591 | TATACAGAAGATGTC[A/G/T]AAGGATAAGGTCTCT | 10451 |
rs139676482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107656182 | ACTATTCATAATAAC[C/T]GAAATATGGAAATCA | 10451 |
rs139682335 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107943351 | AAACTACAAAATTAC[A/C]TAAGATTAGTCCCTC | 10451 |
rs139718082 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728594 | ACAGTCATATGTATA[C/T]GTATACGTATATGTA | 10451 |
rs139720055 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875506 | CAGACTAAAGAAGTG[A/T]TCCATACCAAGGCCC | 10451 |
rs139727371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107833515 | CAAATCTCTCTTCTA[C/T]ACTTTTTCACTTATA | 10451 |
rs139728318 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107781763 | GGTCAACTATGTCGA[A/C]CATCTAATGTCAAAA | 10451 |
rs139731661 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107894678 | TTTTAAAAACGGCAG[A/T]TATAAATATTATAGG | 10451 |
rs139738183 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107946725 | TTCACAACTACATGC[G/T]ATTCCATTATCACTT | 10451 |
rs139767255 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107788855 | CTGCCTTTAAGCAGA[C/T]AGTAGAGAGAATAAG | 10451 |
rs139782969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107596136 | ATATTTTAAAATTTG[A/G]AAGGAAGATGTTTAA | 10451 |
rs139785386 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107878229 | ATACTCTGACTCTAC[A/C]TGCAACTCCCAGGAA | 10451 |
rs139792407 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107900177 | TGGATAGAAATACAT[C/T]TGCTACATAGACTAC | 10451 |
rs139798957 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107687337 | CAAGCACCTCTTATA[C/T]TTTGCTGTACTTTTT | 10451 |
rs139802490 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107838140 | AAACTATGCATCCGA[C/T]AAAGTTCTAATAACC | 10451 |
rs139810300 | in-del | -/AATAAATT | 0.225893 | 0.248835 | intron-variant | VAV3 | GRCh38.p7 | 1:107959268 | TCTGTCTAAAAAATA[-/AATAAATT]AATTAATTAATTAAT | 10451 |
rs139819311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107638500 | TATGACCTTAACTCT[A/G]AAAACTGCAAAACAC | 10451 |
rs139831047 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107759154 | ATTATGAGCTTTATC[C/T]GAGTAGGGTCTGTCG | 10451 |
rs139842367 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107789240 | TTCCAAACTCAGCTC[A/G]CTGTCAAAGTCACAC | 10451 |
rs139852264 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107961473 | GAATACTGTTTCAGA[C/T]GAAAAATAAATCTCA | 10451 |
rs139856964 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107950544 | AGGCACTGCAAAGAG[A/G]TGAATGAAAGCAGGG | 10451 |
rs139857601 | in-del | -/C | 0.109108 | 0.206518 | intron-variant | VAV3 | GRCh38.p7 | 1:107940368 | GCCATGAAGTAGCTA[-/C]CACAACAAGCAAGCC | 10451 |
rs139861998 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107617845 | TGTGGTTTCAGGTCA[C/T]GATCATAAAATAATT | 10451 |
rs139868383 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107846814 | TTAGACTCCCACACA[A/G]TAATAGTGGGAGACT | 10451 |
rs139894223 | snp | C/T | 0.000148374 | 0.00861191 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107603126 | CCCTATTAATAAGTT[C/T]GGTCTCTGCTTGCAA | 10451 |
rs139910788 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107910388 | ACTCCAAGAAGGAAG[C/T]TTTCAGACGATTCTT | 10451 |
rs139942120 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | VAV3 | GRCh38.p7 | 1:107850443 | GGTTGAAGCTGGAAA[C/T]CATCATTATCAGCAA | 10451 |
rs139944095 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107914316 | TCTCGCAACAGTGAC[A/G]TGCAATAAACATTAC | 10451 |
rs139952721 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107856954 | TGAGGCAGGAGGGTC[A/G]CTTGAGCCCAAGAGT | 10451 |
rs139958101 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107841763 | GACACTTGAAATGAG[A/G]CTAGTCTAAATTGCT | 10451 |
rs139959870 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107849402 | ACCAATGGAACAGAA[C/T]AGAGGCCTCAGAAAT | 10451 |
rs139961442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107803437 | ATCCCACAGATTTTG[A/G]TATGTCATATTTCCA | 10451 |
rs139972216 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | VAV3 | GRCh38.p7 | 1:107734974 | AAAACACTCCTCAGC[A/C]AATGTAAAAGAACAG | 10451 |
rs139973721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107688198 | TTCGGACAGTGACAG[A/T]GAACATTCCTTGGAT | 10451 |
rs139976256 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107725865 | GGTCTCCTGGGCACC[C/T]ATAATATCTGGCAGT | 10451 |
rs139988041 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107618929 | GTTTTAGAAGACTTA[A/C]ACTTGCACCAATGTG | 10451 |
rs139988331 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107701156 | AATGGGGTTGTTTGT[A/T]TCTTTCTTGTAAATT | 10451 |
rs139999022 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107793724 | TATTATGATAAGCCA[A/T]TAAAGATATTTTTAG | 10451 |
rs140006871 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107622518 | GTCTCTTCCCTGTGG[C/T]TCATTTATCCCCTTA | 10451 |
rs140008865 | snp | A/C | 0.000287797 | 0.0119923 | intron-variant | VAV3 | GRCh38.p7 | 1:107704693 | ATTAAACGGTGCAAA[A/C]TTCTGCCCATATGAA | 10451 |
rs140026517 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572638 | CCTCTCTTTTGTGTG[C/T]TTTTTTCACCTTTTA | 10451 |
rs140044468 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107882826 | CCCCTGAATTACAAA[A/G]TAAGTATGCTACATG | 10451 |
rs140049093 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107609356 | CATCCTTATATTTTG[C/T]TGCTCTCATATGTTG | 10451 |
rs140053183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693611 | AAAAAGAAGTGTTAA[A/G]AGATACTTCAAATGC | 10451 |
rs140081458 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107867574 | TCCTCCTTTGCCTAA[A/G]AAAAGGTAGCCTTGG | 10451 |
rs140085144 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107613373 | TTGTATCTCATCACT[A/C]CATTTTCTGTTTTAT | 10451 |
rs140099550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107578968 | AGGTAGGTAAATTAG[A/G]TAAGATAACCTATCT | 10451 |
rs140121037 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107936152 | AAAATATGAATTGAT[A/T]GATAAAACATCCTGA | 10451 |
rs140128004 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713174 | ATTGCTGCCTTCATG[-/A]GGCTTATATTCTGCA | 10451 |
rs140153591 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107869167 | ATGTGGTCAAAGGCA[C/T]GGGATATAATTGATG | 10451 |
rs140153799 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107941799 | ATTTGATTTTCTAAC[A/G]TATTCCTCAATGTTT | 10451 |
rs140157387 | snp | G/T | 0.0146672 | 0.084371 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966596 | TATTACGAACCATGC[G/T]TTATAAGCAGGCCAA | 10451 |
rs140163145 | snp | A/C | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570781 | GGCCATCGCCTGTCC[A/C]TTCAGAATGGCGCTC | 10451 |
rs140173144 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107828209 | GGTGGCTCTCTTTAC[A/C]TGTTCTTGCGTTAAA | 10451 |
rs140180363 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107749938 | TTAAAAGCTAAAAAC[C/G]TATAGAATAATATTA | 10451 |
rs140195348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107638797 | TATTAGCTACAGTAA[C/T]CAAGACAGCATCACA | 10451 |
rs140205461 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107840360 | AAAGTTGTGCAAAGA[C/T]CTTTCTTGATTGGCA | 10451 |
rs140208130 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107888452 | TCTCTACCCTGAGAC[A/G]CTTTTTGTTTGTTTG | 10451 |
rs140215561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591835 | TTATTGCTAAATACT[C/T]AGCACACGTTCCTGA | 10451 |
rs140223148 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107907509 | CCCCAATGCAACAGT[A/T]CTGAAAAGTAGGAAC | 10451 |
rs140249200 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107702040 | GCCCCCCACTCTGGG[C/T]ACCAATTTACTGTAT | 10451 |
rs140257222 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | VAV3 | GRCh38.p7 | 1:107910815 | CAAAACCCCATCTCT[A/T]CTAAAAATACTAAAA | 10451 |
rs140257241 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107876482 | AACCTGATAGAGAGG[C/G]GAAAGCTGGTAACAA | 10451 |
rs140260665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795718 | ACATTTGCATAAGTC[A/G]TTAGGGCTTTAATAG | 10451 |
rs140263437 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107879525 | TTTATGGCTAGAGAT[A/G]GGGTGTTTTGGCACA | 10451 |
rs140269125 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107799754 | GAGTCATGCTAACTA[C/T]AGTCACTTTAGTGAT | 10451 |
rs140269482 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107619476 | TGGTATTTGGGACTA[C/T]ACCACTAGCCAGACC | 10451 |
rs140279298 | in-del | -/TGGTCA | 0.434976 | 0.168179 | intron-variant | VAV3 | GRCh38.p7 | 1:107608160 | TAATATTATTCTAAC[-/TGGTCA]TATTTTCAGTAGGAT | 10451 |
rs140279754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902726 | ATCATATCTATGTAT[C/G]AACAAGAGAGGGGAA | 10451 |
rs140289827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107761083 | AATAAAAGAGAACTA[C/T]TTTGTGTATGAAAAT | 10451 |
rs140295922 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107698701 | TGCCAGGAAGAAATA[C/T]CTGAGACTGGGTTAT | 10451 |
rs140315495 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107651636 | CATATACTTGATTAT[A/C]TCTCTAAAATTTCTC | 10451 |
rs140332954 | in-del | -/T | 0.0295035 | 0.117819 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590450 | AGAAGAAATTAAGCC[-/T]ATATACAAATGCCTA | 10451 |
rs140338379 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107776344 | TGAGGAGACAAACAA[C/T]AAATGAAGCAAACCA | 10451 |
rs140339667 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107727139 | GCAAAACAAAAATAG[A/G]TTACAAATAGTTTTC | 10451 |
rs140344886 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107856276 | TTTACATCATTCCAG[G/T]GAAATATCCCACATT | 10451 |
rs140345714 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107790844 | AGGCACCTGCCACCA[C/T]GCCCAGCTAATTTTT | 10451 |
rs140377022 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107780330 | TTTCAGAAAAAGTTT[C/T]CTAAATTAACCTTAA | 10451 |
rs140377065 | snp | A/C | 0.489376 | 0.0721049 | intron-variant | VAV3 | GRCh38.p7 | 1:107737363 | GACAAATGGGATCCA[A/C]TTAAACTAAAGAGCT | 10451 |
rs140379885 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107691439 | CTTAGTTCTGCAATA[C/G]AGCTGAGATAATTAG | 10451 |
rs140385620 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107861084 | TTGGAACTGTTGCTA[C/G]TTAAGAAATTTCTGT | 10451 |
rs140394625 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107657018 | GAGTGCAGTGGCACA[A/T]TCTCAGCTCACTGCA | 10451 |
rs140416425 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107739417 | CCTATCCTGACTTAA[C/G]TGCCAATTTTGAAAG | 10451 |
rs140417762 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107877366 | CTCATAGCTCACCAA[-/G]GAACAAAGCATAATT | 10451 |
rs140432090 | snp | A/G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107611150 | CAAAAATCTAAAATC[A/G/T]TATGTGCTCCAATGA | 10451 |
rs140453020 | in-del | -/CT | 0.239614 | 0.249784 | intron-variant | VAV3 | GRCh38.p7 | 1:107909767 | ATGCAGGTATCCAGA[-/CT]CTCTGCCATGTATAG | 10451 |
rs140459911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107867780 | AATTTGTGGGAAAAT[C/T]CCAGACCCTTGAGGG | 10451 |
rs140465747 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107856644 | TAATTCTCTTGTTTA[C/G]TAACCAGCTTCTCGA | 10451 |
rs140466134 | in-del | -/ACACACACACACAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908821 | CCCCGCCCCACTCAA[-/ACACACACACACAC]ACACACACACACACA | 10451 |
rs140469686 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787111 | TCTCTTCCTTTGCCT[A/G]TCAGAATACCATGGC | 10451 |
rs140469741 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625628 | CAGCTTCTTAGTGAC[A/G]TTTTTAACTCAGTGT | 10451 |
rs140484571 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107853674 | GACACAGAAAGACCA[C/T]CACAGAAAGAGAAAA | 10451 |
rs140489810 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107746366 | CTCCCAATATCTGCA[C/T]AGACATTCAACGGAA | 10451 |
rs140494812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649885 | CATATTTTAGTGGAG[A/G]AGACAAACACAAAAG | 10451 |
rs140495050 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107682102 | TTTAGGATAAAGGAG[C/T]ATAAATCTGTTTTAT | 10451 |
rs140509596 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107631006 | CTTGAAACATTGTAA[C/G]ATCTTAAGTGCTTTT | 10451 |
rs140515141 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107633715 | GGCTTAAGAAGGTCC[A/C]GCAGTTTCCACTTTT | 10451 |
rs140551746 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107578316 | CTGCAGTACATTTTT[-/T]ATTTTTAAGTATACT | 10451 |
rs140556739 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107776753 | GCAGAAGATAATCGG[C/T]TGCAAGGACCTTTTG | 10451 |
rs140565449 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107889745 | AGAATGATGTAGCAC[A/C]GTCTATTCAGGAAGC | 10451 |
rs140577154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774436 | GTGCATGCAAGTGCA[C/G]AAACGCAAACACACA | 10451 |
rs140579073 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107823895 | TGCAAGCCAGGAAGA[C/T]AGCTCTCCAAGAAAC | 10451 |
rs140589333 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911316 | CTTTCTTATGAGCTA[C/T]GTATAAAACATAAGC | 10451 |
rs140591317 | in-del | -/CT | 0.0460142 | 0.144533 | intron-variant | VAV3 | GRCh38.p7 | 1:107661260 | CTTCACGGGGCAGCT[-/CT]GTGACATGTACACAC | 10451 |
rs140593744 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107740145 | TACAAAAATTACCTG[G/T]GTGTGGTGTTGCGTG | 10451 |
rs140596741 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107816241 | TCTATACTTGAATAA[C/T]GACTTGAAAATTGAG | 10451 |
rs140605941 | snp | C/T | 3.303e-05 | 0.00406373 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107770713 | AACAACTTCGTATAT[C/T]ATTTTCTGGACATTT | 10451 |
rs140610196 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107800449 | TGTGATTATTAGTGA[C/T]GCTGAACATTTTTTC | 10451 |
rs140611349 | snp | A/G | 5.16978e-05 | 0.00508392 | intron-variant | VAV3 | GRCh38.p7 | 1:107777347 | AACCCATGAGTGAAC[A/G]AGCAACAATCAGGCT | 10451 |
rs140614264 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107710150 | GAAGCAAATCCTAGC[A/T]AGATGAAATCATCTG | 10451 |
rs140622409 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | VAV3 | GRCh38.p7 | 1:107714863 | CTTAGCTCTGAAAAA[C/T]AGTATTTTCTTATCT | 10451 |
rs140638894 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107627696 | GAATTAAAATCTCAT[C/T]TTATAGAGGAGAAAT | 10451 |
rs140642429 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107717754 | AGATGTCTATTAGGT[C/T]GGCTTAGTGCATTGC | 10451 |
rs140642813 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107673689 | GTCAAAGAGTTGAAA[C/G]AACAAATGAATCAAC | 10451 |
rs140645627 | in-del | -/GCTGATTTAAACA | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107911917 | CTTACTGCAAACAGC[-/GCTGATTTAAACA]AAAATGTAGTGAATA | 10451 |
rs140649587 | snp | A/T | 0.0607341 | 0.163335 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589784 | TGAATTAAAAGGGCA[A/T]GGGAGAAACTAAGTT | 10451 |
rs140669200 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592325 | CACCAAAGTGTTGGT[C/T]TGTCCTGCTTGGAGC | 10451 |
rs140679958 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107584249 | TTACACCTTATACAA[G/T]AATCAATTCAAGATG | 10451 |
rs140715928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677259 | TTAAGAATTACTTTA[C/T]CAATGTCCTCTCCTG | 10451 |
rs140740073 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875079 | TGCTATCCACCCTCT[G/T]TAACACTCAAGACTG | 10451 |
rs140753746 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107794076 | TTAGAAATTTCATTC[C/T]GTTCCAGACGGGACC | 10451 |
rs140774888 | in-del | -/AGTTCCAGGAAACA | 0.079617 | 0.182947 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963156 | AGAGCAACTGCTGAG[-/AGTTCCAGGAAACA]AGTTCCAGGAAATGT | 10451 |
rs140785700 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107706022 | TGGCTTAGCTATTTA[G/T]GTTGCTGCAAAAGTA | 10451 |
rs140791480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755051 | CAGTCCCAGCCCCAA[G/T]CAAAGTGTCTGGGTC | 10451 |
rs140791594 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107797197 | CTATATAGTGTCAGA[A/G]AAATTACCCAAGCAG | 10451 |
rs140793122 | in-del | -/ATT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107884420 | TTTATTATTATTATT[-/ATT]ATTATTATTATTATT | 10451 |
rs140803709 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107877905 | TTCACTCAATGCTCA[C/G]AAGTGTGTGGCTCTG | 10451 |
rs140805288 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107662544 | TTTTTAGAGGCCCAA[C/T]AGTTATCTTTTCTAT | 10451 |
rs140810478 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107575135 | TTTGTTAGTCTCTAG[A/T]GTTTCATGGCACGCT | 10451 |
rs140812854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903488 | TTTGACCTCCAACTC[C/T]ATCATTCATAAGCTG | 10451 |
rs140813786 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107694051 | CTACTCTGAAGGGCC[A/G]CTGAACTCACAGTAA | 10451 |
rs140816918 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107947376 | TTGCCATAGACAAGC[A/G]AAGTTATAGAGTTCT | 10451 |
rs140821903 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107876265 | GCAGTGTGAAAGTCA[C/T]GGGTACCTTGACAAA | 10451 |
rs140828995 | in-del | -/TTTG | 0.337158 | 0.234315 | intron-variant | VAV3 | GRCh38.p7 | 1:107949309 | TTCTTTTTGTTTATT[-/TTTG]TTTGTTTGTTTGTTT | 10451 |
rs140829956 | snp | A/G/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107840867 | GAAGAACTATAAACC[A/G/T]CTGGAAGGAAGTGAA | 10451 |
rs140834074 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107933674 | TTAAAAATTAGCTGA[A/G]TATGATGACACACAC | 10451 |
rs140843676 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107835887 | GACCTCCGGAATTCT[C/G]CAGGTTTCTGGCAAT | 10451 |
rs140851854 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107757461 | TCTAATATGTCTGGG[C/T]TCCATTTCCATCAAA | 10451 |
rs140853199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107697573 | GTTTAGAGAATGATG[C/T]TACTTTTTAATTGAG | 10451 |
rs140859477 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107908448 | TGCTAAAATACCTGT[-/A]AGCAATTTATCTTTT | 10451 |
rs140868663 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107791835 | ACTAGGTTAAGTGAT[C/T]AGTATTATATAATCT | 10451 |
rs140872150 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107722143 | TGTGCTTAAGAGTTT[C/T]GGAGTATGCAGAATG | 10451 |
rs140878573 | snp | A/C/G | 0.00279258 | 0.0372817 | intron-variant | VAV3 | GRCh38.p7 | 1:107906651 | AGCCTGGGTGACAAA[A/C/G]CAAGACTCCATTTCA | 10451 |
rs140882402 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107646202 | CCTCACTGGCAGTGA[C/T]TAATTGGAAACAGAC | 10451 |
rs140891775 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649331 | AGGCCAAGAGAGACA[A/G]TCTAAAGGAGCAGCA | 10451 |
rs140910360 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107795488 | TTGGTACTATTGTCT[C/G]TTTTCTTTTTATTAT | 10451 |
rs140925544 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107729787 | TGATACAAGGAAAGA[C/T]TGGAAAAATAATAAA | 10451 |
rs140931003 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107655438 | AGAACTAAAAATCTA[C/G]ACCCCTATATCTCAG | 10451 |
rs140941425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107924158 | TCTTTCTTCTCTCCC[A/G]TTCCCTATAGAATCT | 10451 |
rs140944812 | in-del | -/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107652841 | CATTTTCCAAAAAAA[-/T]AAAATTGTTTTTGAC | 10451 |
rs140960098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107892433 | ACAGTCCAAGGAGCA[G/T]CTTTTAACCTGAAGG | 10451 |
rs140962227 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107829371 | GCTGCATTCTGTCAG[C/T]AAGCCATGTAAAAAT | 10451 |
rs140963471 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107732470 | TAGCCAAGGGAAGCC[A/G]TGACAGACTATACCA | 10451 |
rs140967909 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107695176 | TAGGAGGAAGTGGTA[A/G]AAAATGAGCTGTACA | 10451 |
rs140974146 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107814179 | TACCCAGTCAGTAGC[A/G]AAAACTGCTGGATCA | 10451 |
rs140975283 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107885123 | CACCAGCCAAGAAAA[C/T]AGCTCCCTGTGAAGC | 10451 |
rs140977409 | snp | A/G | 0.236144 | 0.249616 | intron-variant | VAV3 | GRCh38.p7 | 1:107718313 | TTAGAAAACCCCATC[A/G]TCTCAGCCCAAAATC | 10451 |
rs140977777 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107611506 | GCTTCTGAAATGTGA[G/T]GCGAAAAATATTTCC | 10451 |
rs140996609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107922282 | TAAGGAGGAAATTAA[C/T]GTCTTGTTTTGTGTC | 10451 |
rs140999592 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107678023 | TTATCACGGAAAAGG[A/G]AATCAGAAAGGTAGT | 10451 |
rs141004587 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592788 | AGCTACTCTGGCAGA[A/C]CTCAAAATAATTATG | 10451 |
rs141071315 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107881741 | CATCCTAAAATTATA[A/T]ATCAGGCCAAAGCTC | 10451 |
rs141081066 | in-del | -/C | 0.079617 | 0.182947 | intron-variant | VAV3 | GRCh38.p7 | 1:107723763 | ATGTCTTCCATACTT[-/C]CATATTTCTCTTGGT | 10451 |
rs141082361 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107707089 | ATTATGATGAAAAAG[G/T]TTCTGAAAATATTGT | 10451 |
rs141104165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107844246 | CCCCTAGCCAAGGGA[A/G]GCCTTGAGGGACTGT | 10451 |
rs141106590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107615091 | TAATCTTTCAAGACT[A/G]TAATGTAATATAAGA | 10451 |
rs141113017 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698286 | TTTTGATATTTTCCC[A/G]GGCGAGCAACATGCC | 10451 |
rs141115461 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673204 | TCAAGATTCAAGTGC[A/G]GCTAGGGTGATCTTT | 10451 |
rs141129172 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107658109 | TTCCTTTCAAATTAA[C/T]GGCCTCAATAAAGTA | 10451 |
rs141134245 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107837102 | CAGAGAAACAATGGG[-/C]AAAAAAAAACAAAAC | 10451 |
rs141135543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107575945 | TGCAGAATTCATGGG[C/T]GCCAGTCATCTTTTC | 10451 |
rs141149435 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107897912 | ACTGTTCAATAAAAC[A/C]CAAAGTCTCATAACC | 10451 |
rs141154860 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107894053 | GCACACACAGAATAC[C/T]GATTGGGGCTGCAAC | 10451 |
rs141168109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832669 | TCTTTAACACCTCGG[C/T]AGAAATGGCTCCCCT | 10451 |
rs141170764 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769601 | AATGGCCCAATCTAT[G/T]TGTCAATTCAGTCTT | 10451 |
rs141188453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107785023 | TCTTTATTTTTTTCA[C/T]CCCTTAGTTAATTTA | 10451 |
rs141195601 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107719974 | ACAGAAAACCAAACA[C/T]CGCATTTTCTCACTC | 10451 |
rs141211998 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595061 | CCATTTTTGAATGAG[C/G]AAAAATTATGCCTAT | 10451 |
rs141215896 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107680642 | AGTCCCAAGCTCCTG[G/T]CTTCAAGTGATCCTC | 10451 |
rs141220258 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965520 | GGGCACCCAGACTCC[C/T]CAGAGCAATGAAAAA | 10451 |
rs141224040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885865 | CTGTCCCAAACTAGG[A/G]AGCTGGGAGCTACAG | 10451 |
rs141228011 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107662773 | TGGGTAGAAAAAGAC[A/C]TATTAGTCATATGAA | 10451 |
rs141234456 | in-del | -/AT | 0.190519 | 0.242821 | intron-variant | VAV3 | GRCh38.p7 | 1:107932423 | AGACTATGCAGAAAC[-/AT]GTGAGACTTCAGGTG | 10451 |
rs141238026 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624373 | AATTATAGTCTTATG[A/T]CTGTGTGTGTGTGTG | 10451 |
rs141249756 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107859504 | GTGCTTAGCTGATAA[C/T]AGTCCTAAAATACTT | 10451 |
rs141267283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667354 | AAAAAGCACTGAGCT[A/G]TGCAATGCTAACTAC | 10451 |
rs141282000 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107862873 | TTTCCATTTTTAATA[G/T]AAATGATAAACCCCA | 10451 |
rs141282829 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107929559 | CATTGTAACTATAGT[A/C]AGTAAACTCCCCTAA | 10451 |
rs141296788 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107859815 | AAGTAATGTCTGAAC[A/C]TTTATTCAATCATGT | 10451 |
rs141301497 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107816629 | TAATGCTTGTCTCTT[A/G]ACTCATTTATTTTTG | 10451 |
rs141310662 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107740888 | TATGGCCCACAAAGC[C/T]TAAACCATTTACTCT | 10451 |
rs141311273 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107778763 | CCATGAAACCAGGCT[A/G]AGTAGAGACTGTTTT | 10451 |
rs141323283 | in-del | -/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107843552 | GTATATATATATATT[-/TA]TATATATATATATGA | 10451 |
rs141325860 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107868440 | CCTTTGCTTGGGAGG[A/G]TTTTCTTGTGACAGG | 10451 |
rs141327582 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107710631 | TCTTGCATCCTTCTA[G/T]TAACCTCTATTATTT | 10451 |
rs141328550 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107745511 | CATATTTTAAATGCT[A/G]GAAGTGGTTATGGCC | 10451 |
rs141344204 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107943972 | CCAGGACCAGTGCAT[C/T]CTGCACTTGCTAAGG | 10451 |
rs141353010 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738893 | CTACTCAGACAAGCC[G/T]GAGACAGTAGCACAG | 10451 |
rs141379488 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107960153 | TCTGTTCTCAATGCA[A/G]TAGCCAAAGTAACTG | 10451 |
rs141400765 | snp | C/T | 0.211819 | 0.247067 | intron-variant | VAV3 | GRCh38.p7 | 1:107728612 | ATACGTATATGTATA[C/T]GTATATGTATATGTA | 10451 |
rs141405647 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107830564 | ACCTCATTCTGCACA[C/T]AGCCCCCTCCAGCAT | 10451 |
rs141412135 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107909834 | TGAGAAAATCTTTCT[A/C]ATCAGTGAAGAATAC | 10451 |
rs141413384 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107846054 | CAGTCAGAGAGAAAG[C/G]TCAGGTTACCCACAA | 10451 |
rs141419053 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107632841 | TGTTTCTAATCATTA[C/T]ATATACCCCAGACAT | 10451 |
rs141424199 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107752510 | CAATATCAACAGAGT[A/G]AAAAGCCAACAGACA | 10451 |
rs141425027 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107713961 | TGAAATTTAACGTTT[C/G]TGCCGAATGTTCAAA | 10451 |
rs141433808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797275 | TTATAACACTAGTTT[A/G]CCTCTTAGTAATTCT | 10451 |
rs141444014 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107835184 | CAGCCGCTATCAAGG[C/T]CCCTGCCTGGCTGCT | 10451 |
rs141457272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588288 | AAGAATATAAAAATG[A/T]CAGCAATATGTTATA | 10451 |
rs141464207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756330 | ACAGTAGGGACAGAA[C/T]TCTGCAAAAAGCAGT | 10451 |
rs141464499 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | VAV3 | GRCh38.p7 | 1:107719538 | CACCAGTTAGAATGG[C/T]GATCAGTAAAAAGTC | 10451 |
rs141473876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807920 | CTCTAAAGAAACTTG[C/T]ACATTTACAAATAAG | 10451 |
rs141477879 | snp | A/C | 1.72618e-05 | 0.00293779 | missense, intron-variant, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107688388 | AATCTTACCTCTGGT[A/C]GTTTGAGTGTCCCTT | 10451 |
rs141490372 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107900162 | TGAAACAGTTACACA[-/T]GGATAGAAATACATT | 10451 |
rs141495660 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107621291 | TTAACCTATTTTAAC[A/G]TATGAATAAAGTTAC | 10451 |
rs141495935 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107645645 | GAAGACAAAAAATTG[A/C]GATTAAGAGGAAATG | 10451 |
rs141504381 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107721902 | GTAGTCCCCAAATAC[C/T]TCCCTTAAGAAAATG | 10451 |
rs141509293 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107872764 | TGAGTTCAAACTGCT[C/G]CTTCAATCTCAAATA | 10451 |
rs141512038 | in-del | -/AATC | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107778373 | CTTACGTTTTTTCAG[-/AATC]AATACATAAAAATTT | 10451 |
rs141535816 | in-del | -/TTTTG | 0.206642 | 0.246211 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963747 | GAAAGCAGTTTGGTT[-/TTTTG]TTTTGTTTTAACATT | 10451 |
rs141539168 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107793536 | CATGGCACACAGATG[C/T]TCAGTAACTACATCT | 10451 |
rs141545120 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107703442 | TCATGCAAGAAGATG[C/T]CCAGTAGAGCACCCA | 10451 |
rs141569623 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571376 | CAAAGATGTAATTGG[C/T]AATGTCACAAAAAGG | 10451 |
rs141574325 | in-del | -/TGT | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107774069 | TTTCTCTATTTTTGC[-/TGT]TGTTGTTGTTTGGGG | 10451 |
rs141577069 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693040 | CTGGGATTAGACCTT[C/T]GCGGTGGTGTACTGT | 10451 |
rs141610076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695870 | TCTGTCCATTAAAAG[A/G]TAGAGTAAAAGATTA | 10451 |
rs141610227 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107642348 | AATGCCATGGCAACG[C/T]CAGGAAGTTACCCAA | 10451 |
rs141615527 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107667697 | CCCTGTTTTCTACAC[-/A]AATCTTAATGAAGAC | 10451 |
rs141620336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757775 | CATCCTAAATTTCTG[C/T]CTCCTCCTCAGTCTT | 10451 |
rs141639917 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107598854 | CTGATACAAACGATA[C/T]CGAAGTTTCTCCTAG | 10451 |
rs141653348 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107647844 | AAATTAACATCTGGA[C/G]CTTTCCTGATACAAG | 10451 |
rs141676002 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107604543 | CTCAAGCTCCTTTTG[A/C/T]GCTTAGGGTCTTCTC | 10451 |
rs141680364 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107652459 | CTTTCACTTTACTCT[A/G]TGAACTCACCTGAAT | 10451 |
rs141693897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107638067 | AATGTCCTCAACTTA[A/T]TGAAGGGCATTTATG | 10451 |
rs141713761 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | VAV3 | GRCh38.p7 | 1:107833513 | TTCAAATCTCTCTTC[C/T]ATACTTTTTCACTTA | 10451 |
rs141730079 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107882190 | TTTCATGAGAAGGTC[A/G]GTGAGTGCTAATAGA | 10451 |
rs141737262 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914328 | GACGTGCAATAAACA[C/T]TACTGGGCCCTGCCT | 10451 |
rs141749083 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107919477 | TAAATCAGACAAGTA[C/T]AAAAAGTCTAAGAAT | 10451 |
rs141758137 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962725 | GCACCCTCTCATAGG[A/G]CATTACAGGAGAAAC | 10451 |
rs141789256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107712180 | TAACTTGACAAATGA[C/T]TATAAAATACAACCA | 10451 |
rs141798560 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107810087 | ACAATTTTCAACAAA[A/G]GAAAAGACTGATTAG | 10451 |
rs141806440 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107599183 | ACTCTTTATCACTTC[A/G]CTAAGCATGGAAGAT | 10451 |
rs141807272 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107914021 | GCAGGTCTCAAACTC[C/T]TGACCTCAGGTGATC | 10451 |
rs141808723 | snp | A/G | 0.000342247 | 0.0130769 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964847 | TGGATGAGCCACTGC[A/G]CGCACTGCTTCCACG | 10451 |
rs141815428 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107586562 | ATCAGTCAGGCAATA[C/T]TGAAATTTTTGTGCC | 10451 |
rs141826350 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107848245 | GTGAACCCTGGAGGC[A/G]GAGCTTGCAGTGAGC | 10451 |
rs141826818 | in-del | -/A | 0.26306 | 0.249659 | intron-variant | VAV3 | GRCh38.p7 | 1:107639381 | CATTATCAAGAGAAT[-/A]AAAAAAAAGCCACAG | 10451 |
rs141836959 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107803019 | GCTTCAATCTTGTTG[C/T]TCCTTATTGGTTTGC | 10451 |
rs141838916 | in-del | -/CCCC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954703 | AGGTGCTATTAACAA[-/CCCC]CAGCCATAAGGCCAA | 10451 |
rs141839350 | snp | A/C | 0.0275645 | 0.114116 | intron-variant | VAV3 | GRCh38.p7 | 1:107880784 | CTGGGCAACAAAGTG[A/C]GATTCTGTCTCCAAA | 10451 |
rs141867426 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107851884 | GCTATTTTACGAGTT[A/T]GCTGATTTTTTTAAA | 10451 |
rs141877561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107663736 | TAATTTCAGCAAATA[A/G]TGTCATAGTAATACT | 10451 |
rs141882107 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773507 | CCCACCAGTCCCCCA[A/T]CAACCAGACCCTTCC | 10451 |
rs141883654 | snp | C/G/T | 0.00756609 | 0.0611252 | intron-variant | VAV3 | GRCh38.p7 | 1:107732867 | AGAGCAGTGGTTCTC[C/G/T]CGGCATGGTGTTTGA | 10451 |
rs141884557 | in-del | -/A | 0.114387 | 0.210022 | intron-variant | VAV3 | GRCh38.p7 | 1:107614479 | ACTTGCCCTATAATT[-/A]AAAAAAAAAATCTAT | 10451 |
rs141896156 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107770159 | TTCCAATCAGAGGGG[C/T]TCTCTCGGGAATGAT | 10451 |
rs141902233 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107708264 | CAAGCGTGGATATAG[C/T]AGGACCAATCATGGG | 10451 |
rs141912079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667866 | CTCTATGTGGAATGA[A/G]CTTCCTTCCTTGCTT | 10451 |
rs141912683 | snp | A/G | 0.000298359 | 0.0122103 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107760799 | CTGGAGGAGAAGGTG[A/G]TACTTTAAAACACGT | 10451 |
rs141921551 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107735882 | ATCCTGATACCAAAG[C/T]CTGGCAGTGACACAA | 10451 |
rs141922135 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107664504 | GCAGCAGCATAGGTC[A/G]GCTTTTCAAAAAGGT | 10451 |
rs141932030 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107885209 | TTCCTCATTAGAGTA[C/T]AACATTCAAAATGAG | 10451 |
rs141933405 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107877346 | TTACATAATTAAGTG[C/T]CTGACTCATAGCTCA | 10451 |
rs141945610 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814747 | CATAATAATTTTGAG[C/G]AATGCAGAGGTATGA | 10451 |
rs141947705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767980 | TAAATGGGAGTTACA[C/T]ATGATACAACTGGAA | 10451 |
rs141959934 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107758447 | CAAGGTGGCATGAGC[C/T]TGTAGTCTCAGCTAC | 10451 |
rs141966020 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107837648 | AACTACACTACAAGG[C/G]TACAGTAACCAAAAC | 10451 |
rs141985717 | in-del | -/GAAG | 0.278133 | 0.248412 | intron-variant | VAV3 | GRCh38.p7 | 1:107687032 | AATGAGAAAGTGAAA[-/GAAG]GCTGCTTTGCAAGAT | 10451 |
rs141989102 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107708868 | ATCATGACCAATTTC[A/G]GTCAATTCAAGCTTA | 10451 |
rs142018599 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107711787 | CTGCCTCCCAGGTTC[A/G]AGCGATTCTCATGCC | 10451 |
rs142018685 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107664905 | TGTTCAGAAACAAGA[C/G/T]CATGACCCAAGGTAT | 10451 |
rs142039134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579197 | CCACCCAAACAGTAG[C/T]TAGCCCTCACAGTTA | 10451 |
rs142052485 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107673031 | AGATATTGTACCTCT[A/G]TGACGCCATTGTTAA | 10451 |
rs142052660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107620402 | TGTTTAGATACACAA[A/G]TGTTATAACTACCTA | 10451 |
rs142055075 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107881595 | ACAACCATGCGTAGC[C/T]TCTCTCCCTCTTCAG | 10451 |
rs142059121 | snp | G/T | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107776364 | GAAGCAAACCAAGAC[G/T]GTCTCAGGCATTGGC | 10451 |
rs142074929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107585358 | TGTCATCTATTTTCA[C/T]GGTTTTTTTTATTAT | 10451 |
rs142082399 | snp | C/T | 8.25934e-05 | 0.00642572 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642641 | AACAGACTGTGTGCA[C/T]CTCCTTTCAGAAGTT | 10451 |
rs142083483 | snp | A/T | 0.029116 | 0.117091 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107587961 | TAATGAACAGTATAA[A/T]AGATGAGAAATTCTA | 10451 |
rs142084966 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107673035 | ATTGTACCTCTATGA[C/T]GCCATTGTTAAATAA | 10451 |
rs142092259 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107622900 | TTGGATGGGCAGATG[G/T]AAGGAAGGAAGGATG | 10451 |
rs142130388 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107942140 | TTCTTCAGTATGTTA[C/T]GCTGGCATCGCTGGG | 10451 |
rs142132781 | snp | C/T | 0.000153988 | 0.00877328 | splice-donor-variant | VAV3 | GRCh38.p7 | 1:107768440 | GCATATTTTTACTCA[C/T]AGGAATGTTGATGAA | 10451 |
rs142136586 | in-del | -/GTTTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107872912 | TGGTGGTATTGGCAG[-/GTTTT]TTTTTACTTAGAGTA | 10451 |
rs142143197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107951528 | ACTCTCAACAGAGTA[A/G]AGAGACAACCTACAG | 10451 |
rs142147685 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107893588 | GGCAAAAAAAGCTTC[C/T]GGAGGGAAACTCTCC | 10451 |
rs142152838 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107873292 | CACCATGCATTTTAA[A/C]GTATTTATATATTTT | 10451 |
rs142153214 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107850700 | CATTCTGCACATGTA[C/T]CCCAGAACTTAAAGT | 10451 |
rs142155057 | in-del | -/AAAACAAAAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107793296 | CCACAAAAACCAAAA[-/AAAACAAAAC]CAGCCTGTCATGAAC | 10451 |
rs142162211 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107879232 | TAAGTCTTATTTTCA[C/T]TTATACAATAAATAG | 10451 |
rs142162571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107772522 | TTTCCTTACTAGCGA[A/G]ATGAAAAGACTAGAC | 10451 |
rs142176944 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107839696 | AGGAATCAACAAAAT[C/T]GGAAACAGGTAAACA | 10451 |
rs142184111 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107764460 | TCTCTTCCTTCCTGT[A/G]GGCAATATGCATGGC | 10451 |
rs142191903 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107666991 | TCATAAGCCAAACAT[A/G]TAAGAGCCAGCAGCT | 10451 |
rs142199672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107833475 | GACCAATCCTTTTTA[A/C]AGAAAATATTATCAC | 10451 |
rs142202500 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107811651 | GATAACTGGAATTCA[-/T]TAAAAAAGCAGAACT | 10451 |
rs142212368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619069 | TATTTAACTAAGTCT[G/T]CTGAACTGGCCAGTG | 10451 |
rs142223866 | snp | A/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107843732 | CCCCCATGGGGTTAT[A/T]CCAGACTGATAAAAT | 10451 |
rs142233633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787626 | ACCCCTCTCATCATC[A/G]CATCGTACTCCAGTG | 10451 |
rs142243892 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107868207 | TCTGGATAATTTGAG[C/T]GGGAAATACTTCAAG | 10451 |
rs142245622 | snp | A/G | 0.000625999 | 0.0176807 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574093 | TTTGCACTCATCTTT[A/G]TGTAAATCTTCACCA | 10451 |
rs142251447 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946446 | TAACCAAGACTTTGG[A/C]AATCTGTGCTTTTTG | 10451 |
rs142276919 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107790428 | TGGGAATCAGACAAG[C/T]AAATAGTCACAAAAA | 10451 |
rs142281530 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107834528 | CACAATAGCAGAATA[A/C]GCATTCTGATCAAGC | 10451 |
rs142284611 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896333 | CCATCCCCACCCCAC[A/C]CAAGAGCTATCAATC | 10451 |
rs142287137 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107731424 | CTTTTCATTTATTCA[C/T]AAAACAATATGTTTT | 10451 |
rs142288601 | snp | C/T | 1.65018e-05 | 0.00287239 | intron-variant | VAV3 | GRCh38.p7 | 1:107683462 | AGCTGAAGCCATAAT[C/T]ATGGAAGGTTTAATC | 10451 |
rs142288645 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107870676 | CTTTCTCTCTCTCTC[C/T]CCCAATAATGTTCTT | 10451 |
rs142302441 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786566 | AAGAATGTCCTATAC[C/T]TCTGCTGCTATTTCT | 10451 |
rs142312683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721566 | CACATCAGACACTTC[A/G]GAAGGAAAGAAACAT | 10451 |
rs142317282 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107690698 | ATGCTCTACACAAAG[C/T]CTTCTCTGTGTAACC | 10451 |
rs142318868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613967 | TTAGAATTATTTAGG[C/T]AGTAGAGCTGGTATG | 10451 |
rs142325628 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107898282 | GAGTTCCTCTTATTT[A/C]TGCTCTCTTCATAAG | 10451 |
rs142331597 | in-del | -/TATA/TATATA | 0.359998 | 0.2245 | intron-variant | VAV3 | GRCh38.p7 | 1:107952468 | CTTATAACAAAACTT[-/TATA/TATATA]TATATATATATATAT | 10451 |
rs142341952 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107836994 | GAAAAACTGGTACCA[A/G]TCCTGCTGAAGCTGT | 10451 |
rs142356795 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107681952 | GGCGTGAGCCACTGC[A/G]CCCAGCCACGTATGT | 10451 |
rs142369115 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107751690 | GGGGGGGCGCGCGCT[A/G]ATTTGGTCTATAAAG | 10451 |
rs142382633 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107788757 | TGTTAAACTTAGTAC[A/G/T]CAAATGATAAAGAAT | 10451 |
rs142394992 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963251 | CCTCCTGAGGCTACA[A/G]GCAAAGTGGAAAATG | 10451 |
rs142404663 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107892050 | AAGCAATAAGCTTTC[A/G]CTAAATATTACTTAC | 10451 |
rs142422440 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107640181 | GAATGTTCATAGAAG[A/C]TTTATTTGCAATAGC | 10451 |
rs142431204 | snp | A/C | 0.0528381 | 0.153711 | intron-variant | VAV3 | GRCh38.p7 | 1:107781584 | AGAGAAGGGAGCAAA[A/C]CTCTTTAGGATAGTT | 10451 |
rs142436520 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107861998 | GCTCTACGCACTGGC[C/G]TGTCCTGACACCACT | 10451 |
rs142439664 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107727679 | CAGCTAGCCATATTT[C/T]AAATTAAATATAAGC | 10451 |
rs142448350 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107693448 | AATACAAATGAGGTG[C/T]TTCATTCAGAAATGC | 10451 |
rs142449265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107601735 | TTTAAATGACATACA[C/T]AAAATATTCTTATAT | 10451 |
rs142458602 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107866781 | TGAGCCGAGATTGTG[C/T]CACTGTACTCCAGCC | 10451 |
rs142462795 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107675982 | CATTTTGGATACCAG[A/G]GAACTATCAAACAGA | 10451 |
rs142472390 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107644858 | ACTGGAATGCCCACC[A/G]CATGCCCATAACATG | 10451 |
rs142481290 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107962301 | TCACTACAGCTAGAA[A/C]CTTTCCCAAGAAAGA | 10451 |
rs142481832 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107692519 | TCAATCTTCAGCTCA[C/T]GTAAAAGTACTGTGA | 10451 |
rs142488326 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107910816 | AAAACCCCATCTCTA[A/C]TAAAAATACTAAAAT | 10451 |
rs142499589 | snp | A/C/G/T | 0.00274728 | 0.0369663 | synonymous-codon, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964861 | CGCGCACTGCTTCCA[A/C/G/T]GGCTCCATGCCCGAC | 10451 |
rs142501153 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847949 | CCAACACCTGGCAGA[A/G]ACACAACAAAAAACA | 10451 |
rs142504300 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107739732 | ATGCCAGTAAGGCCT[C/T]CAGTTTCCAAACAGA | 10451 |
rs142512806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912288 | TAATGCTTTGTTGCT[C/T]TGTAATTTTGAGGAA | 10451 |
rs142536339 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107626510 | GAGCCTCTACACTTT[A/C/G]ACATAGCTTTTTATC | 10451 |
rs142539338 | in-del | -/GAGA | 0.216048 | 0.247684 | intron-variant | VAV3 | GRCh38.p7 | 1:107952521 | AAAAAAGAAAGACAG[-/GAGA]GAAATACCTTGAGCC | 10451 |
rs142541588 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107855612 | TTAAATTTGTTAAGA[A/G]CAGGGGCAGGAATTG | 10451 |
rs142566026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107852472 | AAGCTTCCTTCCAGG[C/T]TTACATATATAATCT | 10451 |
rs142570031 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107885380 | TGAATTCTGTTATGC[C/T]GTAATTTGAACTCTC | 10451 |
rs142595791 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107906381 | TATAAAATAACAAAT[C/T]GGGCTGGGCACGGTG | 10451 |
rs142595955 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591172 | ATCCTTTAAGTTTAG[C/T]CTGACTGTCACTTCT | 10451 |
rs142604547 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107806716 | AACCTAACATAACCA[A/C]AAATGTTATAATGTA | 10451 |
rs142614854 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107811813 | AGGTGATAAACATCC[C/T]GCAACTCAGGGCTCC | 10451 |
rs142622124 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | VAV3 | GRCh38.p7 | 1:107736123 | ACATGATTATCTCAA[C/T]AGATGCAGAAAAGGC | 10451 |
rs142625003 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107795433 | TATTGGCTTCTGTGC[A/G]ATGGTATTTGTGATC | 10451 |
rs142629830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875606 | AAAAGGAGGAAAGAT[A/G]GAAAGCTAGTGGGGT | 10451 |
rs142633687 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107887191 | GTCCAACCTGGCAGC[A/G]AGCAGTAGCCATGAG | 10451 |
rs142635458 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107771548 | GCGAGCTACCGCGCC[C/T]GGCCTGTTGTTAGCT | 10451 |
rs142637178 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107622794 | TGTCAGAAATACACA[G/T]GTTGAGTGTTTGGGG | 10451 |
rs142641113 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107705775 | CATCAATCCTAACTG[A/C]CTGGCACGAATAATA | 10451 |
rs142642171 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107813045 | GGAGAATGGCATGAA[C/T]CCAGGAGGCAGAGCT | 10451 |
rs142655808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702880 | CAGGTACTGTGGTAA[A/G]AATCAACATTATCTC | 10451 |
rs142665692 | in-del | -/C | 0.0659589 | 0.169201 | intron-variant | VAV3 | GRCh38.p7 | 1:107836460 | AGCACTAAATGCCTA[-/C]CATCAAAAAGTTTAA | 10451 |
rs142668144 | snp | C/T | 8.23906e-05 | 0.00641783 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574162 | GCACAGAAGTCATAC[C/T]GAGCGATGGCAATGC | 10451 |
rs142680761 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107571002 | GTCCACGGGGCTGGC[A/G]GGCGGGGGGGTGGTG | 10451 |
rs142707429 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107861398 | ACTGTACTTTATCAT[C/G]TGGCAGCCAATAAAT | 10451 |
rs142711478 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107927365 | TGAGACTCACGACAT[C/T]CCCAGCTGTGGTGGC | 10451 |
rs142727230 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864454 | TGGCAAAACCCTGTC[G/T]CTACAAAAAAATGCA | 10451 |
rs142742403 | in-del | -/TC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107870664 | TAAAATACAACTCTT[-/TC]TCTCTCTCTCTCCCA | 10451 |
rs142755296 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107742483 | ACAAAAGATAATTTC[A/C]TTCTTTACTTAGCAT | 10451 |
rs142756796 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107854692 | CTTTTGCAGTATGTC[A/G]TAATGACCTCCCTGA | 10451 |
rs142771368 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107934448 | ACAGGCTATGTGTAT[A/G]TGTGTGTGCATCCTT | 10451 |
rs142783200 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107631844 | AGTATTTCATGGTGT[A/G]TATCTGCCACATTTT | 10451 |
rs142799141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107870074 | CACATTTTTGCAATT[A/G]TGAATTGTGCTGCTA | 10451 |
rs142800648 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107820157 | AGAGATATCTGCACT[C/T]CCCTGTTTATCACAG | 10451 |
rs142806342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107670782 | GTCACACTACAAATA[C/T]GAGTAAAGTGCCGAC | 10451 |
rs142816342 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107736444 | CAGATGACACGATTG[C/T]ATATTTAGAAAACCC | 10451 |
rs142818490 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942494 | TGTCTCACTTCTTCA[C/G]GCCCACCACACTTTC | 10451 |
rs142820345 | snp | A/G | 0.000165027 | 0.00908221 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642670 | TTCAACGGTATCCCC[A/G]GCCTGGAGCTGTAAA | 10451 |
rs142822312 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107825525 | AAATGTAGGCAGGCT[C/T]ATGATAGAGAAAAAT | 10451 |
rs142836941 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107621675 | CATTTTATTCTGGGT[C/T]AGATAATCAGCTTGT | 10451 |
rs142839886 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107738225 | GAGGGAATGGGGGAG[A/G]GATAGCATTAGGAGA | 10451 |
rs142846044 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107751503 | AATTACGAGACGGTT[C/T]GGCAATTAATATTTT | 10451 |
rs142850625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107829148 | TAAAATAAACTAAAT[A/G]ATTTGTGAAAAGAAT | 10451 |
rs142863968 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107655796 | ATGAGCTAAAGATCT[A/G]AGTAGACATTTCTCA | 10451 |
rs142871436 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107636948 | ACTAGCAAAAGAAGA[G/T]CAAATTAAGCCCAAA | 10451 |
rs142872639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624826 | TGCACAAGGCACTGT[A/G]TTACATACTAAGGAA | 10451 |
rs142873612 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107715418 | AGTATAAATGATCAT[C/G]TATGTATTACTATAT | 10451 |
rs142908064 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107578418 | TTTTCATTTTCTTGA[A/G]ATCATGATATAATTT | 10451 |
rs142911170 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590842 | AAAGCATGCTTATCC[C/T]TCTCACGGACATCTG | 10451 |
rs142935195 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107935862 | GAAAGAAACCATGGT[A/T]TATCAGGTGATGGTC | 10451 |
rs142952941 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592990 | AGAGGAAGCCCAAGA[C/G]CTCCCTGCTATGCCT | 10451 |
rs142953396 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107821594 | GCGTGTTCTAGGAGC[C/T]GGTAGACAGCTGACA | 10451 |
rs142962035 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107899079 | ATGAAGATGATGAAA[A/G]TATGTATGTGGTTCT | 10451 |
rs142963462 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107648561 | GGCAAACAGCTATTC[C/T]CAGGGATGTAAGGAA | 10451 |
rs142982139 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107602812 | AATATACACACATCA[A/T]ACCACCAAAACACAA | 10451 |
rs142988349 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107915400 | GATAAACCAGGTGCA[A/G]GTTATGACTATCACC | 10451 |
rs142993792 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107888514 | CGCAGGCTGGAGTAC[A/T]ATGGTGCAATCTAGG | 10451 |
rs143001730 | in-del | -/TTA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107884406 | TTAAAAATAAATTAT[-/TTA]TTATTATTATTATTA | 10451 |
rs143006923 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107877956 | TGAGGAATAGAGGAA[C/G]TGAGGCTGCCAGCCT | 10451 |
rs143014399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107806279 | ATGAGTTGTGGAACA[C/T]TTTCCATGTGCTTGC | 10451 |
rs143017618 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107868767 | TAAAGATTAACACAT[C/T]TACAAACCTGAAATC | 10451 |
rs143025679 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107903809 | CTGACACCTCCATTT[A/G]TGTAAATAAATTAAT | 10451 |
rs143034326 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107765647 | TAAGGAACATAAATC[A/T]TCTGAAGAGAGGAAA | 10451 |
rs143035545 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107788951 | TGTAGGTAAACACCA[A/G]TTAGTCACTGAACCA | 10451 |
rs143045580 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107702635 | CTAGGAATTTTCAAT[C/G]ATTTCCTATTGACTT | 10451 |
rs143051084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107584959 | ACTGCTAAGATATCA[C/T]AGGAGATATAATGAA | 10451 |
rs143057909 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753215 | CCAGTCATGAAATGG[A/C]AAATATTGTATGATT | 10451 |
rs143064842 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657471 | TATCTCAGGAAATAA[C/T]GAGCACTATAGAAAA | 10451 |
rs143070546 | snp | A/G | 0.000117234 | 0.00765529 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749480 | TTTGTTTTCTTTATC[A/G]GTTGTAGGATTATTG | 10451 |
rs143072546 | snp | A/G | 0.00836139 | 0.0641154 | intron-variant | VAV3 | GRCh38.p7 | 1:107792224 | AAGCAAGTGTTGAGT[A/G]TTTTTTTTCTTACAT | 10451 |
rs143077416 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107880603 | GAGCTCGAGACCAGC[C/G]TGGCCAACATGGCAA | 10451 |
rs143102806 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107831462 | AATTTTTCTTCCATA[C/T]ATATTGCAATGTTTA | 10451 |
rs143116427 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107957453 | ATGGAGCCACTGTAA[C/T]TATAGAGGCAGGGGT | 10451 |
rs143123480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761760 | ATGTAATATCTACTC[C/T]AATATGATTTGTGCT | 10451 |
rs143148082 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107954239 | AAAATGCCCTATCAA[A/G]GCACATCATTTTAAA | 10451 |
rs143165678 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107651214 | AACTGTCAGCTGTCA[A/T]TTATAAACCACAGAG | 10451 |
rs143170842 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107726629 | ATCAAGGGTTTACAG[G/T]TAATTTCTTTGGCTT | 10451 |
rs143177815 | in-del | -/TG | 0.281313 | 0.248031 | intron-variant | VAV3 | GRCh38.p7 | 1:107753475 | GTGTGTGTGTATGTA[-/TG]TGTGTGTGTATATAT | 10451 |
rs143178784 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107937402 | CTTCAAACCAAACTT[C/T]CATCTCTGCCTGCCA | 10451 |
rs143185100 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107906974 | ATGAAGCATGGGTGG[A/C]GGTCCAAGTATCTTA | 10451 |
rs143185132 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107961612 | GTATAACTAAATATG[A/G]TTAATGTTTACCTCT | 10451 |
rs143186469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107605723 | AAAATATTACATAAA[A/G]TTACCTTCAGGCTTT | 10451 |
rs143204424 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107841516 | ACAATCTTTCTCCAC[C/T]CCATCACTGCTTGTG | 10451 |
rs143206981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824462 | TGTACATTTTCAGAA[C/T]CAATGTACAAGGTAT | 10451 |
rs143210507 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107638557 | TGAGGAGTATAGTAT[A/G]TTCAGTGATTAGAAG | 10451 |
rs143211862 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107890666 | CAGACACCTTTAGTC[G/T]GCCTTCTTTGAGTCA | 10451 |
rs143223142 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107959292 | ATTAATTAATTAATT[A/G]ACCCATATATTGATT | 10451 |
rs143228120 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107778273 | AAATGTAGTCTCATA[A/C]TCATTTTTTATAAAT | 10451 |
rs143229957 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107846864 | ATTAGACAGATCAAC[A/G]AAACAGAAAATTAAC | 10451 |
rs143231047 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107714733 | CAAGTTTAAAAAAAA[A/C]AGTTCAGAAGGGACA | 10451 |
rs143235389 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107715083 | AAATTAAAGTGTGGC[C/T]TTTGGCCCATAAACT | 10451 |
rs143256751 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107674027 | GGACAACAAATATCT[A/C]TTGTATTTCTGTCAC | 10451 |
rs143257550 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107655517 | CTCAAACTATGAAAC[C/T]ACTAGAAGAAAACCT | 10451 |
rs143261596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107766748 | AAGGGGAGGAAGCAG[C/T]GGGAGAGGACAGGGT | 10451 |
rs143269617 | in-del | -/CTT | 0.214793 | 0.247509 | intron-variant | VAV3 | GRCh38.p7 | 1:107726552 | GTAACATCAAAAAGC[-/CTT]CTTCACTAAAAGCTA | 10451 |
rs143296443 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107658287 | ATGAACTCATCATTC[C/G]TTATGGCTGCATAGT | 10451 |
rs143299344 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107910487 | AAGCCCCAATTAGCA[C/T]TGCTGCAGTGACAGC | 10451 |
rs143302215 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107730489 | CAAATAAAATCAAAC[C/G/T]GTTGCATTAATCATA | 10451 |
rs143304162 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107886604 | TTCAAGAAATCTAAG[C/T]GGATAGGTTTTGTAT | 10451 |
rs143328426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953891 | AACTCTCATGTGAGT[A/G]GCATGTGCTGCTGGC | 10451 |
rs143329766 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107773737 | TGAGGGGTTTAGGCG[G/T]CAATCTGGCCAGAGA | 10451 |
rs143332310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613111 | TTGTTGCTTCTATTA[C/T]TTCTGTTGTTAGCTG | 10451 |
rs143333654 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107852672 | TGTTAGTTTTTATTC[C/T]AAATTATTAAATTAA | 10451 |
rs143345312 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107841392 | TAAAGGGCACAGAAA[C/T]TGTCAGAAGGCTGAG | 10451 |
rs143349593 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736150 | AGGCCTTCAACAAAA[G/T]TCAACAGTCCTTCAT | 10451 |
rs143356608 | snp | A/G | 0.000777907 | 0.0197066 | intron-variant | VAV3 | GRCh38.p7 | 1:107669520 | TCAAGAATGCCTGAA[A/G]ATTTCACCATGGATC | 10451 |
rs143374959 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107621007 | GAGTAAATGGGTAGT[G/T]ACTAATAACTATGCC | 10451 |
rs143379600 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107881119 | CTCCATTTTTGCAGC[G/T]TATAGAATTAAATGT | 10451 |
rs143386203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107904068 | TAACTTTCCACCTTA[C/T]GTGCTCCATCATTTC | 10451 |
rs143391394 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107804339 | TACTGTCTTCCTTTG[C/T]GGTTAAGTGACTTCC | 10451 |
rs143408448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107935270 | TTATTTGATTTCATT[C/T]AAGTGAATAAATATT | 10451 |
rs143422126 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107939245 | AGAAACTAAATCTCC[C/T]TGCAAGTCCAAAAAT | 10451 |
rs143433097 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107763000 | ATCTTGGTTCCAAAG[C/T]AGAGAAGAAAAAGAC | 10451 |
rs143445436 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107701870 | TGTCCACACCATTAT[A/C]AGCACTTTGGTCAAA | 10451 |
rs143456026 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107800056 | AATAATATTCCATTG[C/T]GTACATATATCACAT | 10451 |
rs143456539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107820903 | TTTCTTTAATACCTA[C/T]ATAACCAAGAGAAAA | 10451 |
rs143463344 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726804 | AGATGGAATAAAGCC[-/T]GCTAATTGAATTTTA | 10451 |
rs143471204 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107826220 | ATATTGTAAATCCCT[A/G]TCTACACGATTAGGT | 10451 |
rs143482274 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | VAV3 | GRCh38.p7 | 1:107698989 | TACAATTCGAGATGA[C/G]ATTTGGGTGCGGACA | 10451 |
rs143485651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656315 | CTGTCATTTGCAGCA[A/G]TATGAGTGGAACTGG | 10451 |
rs143493312 | snp | C/T | 9.88908e-05 | 0.00703105 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107596276 | CTTGTATGGAAACTG[C/T]AGAGTTGTATCTAAG | 10451 |
rs143507466 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | VAV3 | GRCh38.p7 | 1:107812906 | AGGCAGGCGGATCAC[A/G]AGATCAGGAGATTGA | 10451 |
rs143513643 | in-del | -/AAG | 0.114036 | 0.209795 | intron-variant | VAV3 | GRCh38.p7 | 1:107840345 | AACATGTATATTTTA[-/AAG]AAGTTGTGCAAAGAC | 10451 |
rs143518938 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788486 | ACTATAATTTACAGA[C/T]GCAATTTCAAAATTA | 10451 |
rs143524017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107868496 | ATAGACAGGTAGTAG[C/T]AAACCATTGCAGGCT | 10451 |
rs143530027 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107716039 | GACAAGCTTTGTTAA[A/C/T]TTTTCCTCTTCAAAT | 10451 |
rs143538087 | snp | G/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107844350 | ATTCCATCTGGTGCC[G/T]ACACCACCAGGGCCC | 10451 |
rs143546591 | snp | A/C | 0.0023933 | 0.0345097 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573158 | ATTAATCTGTCAGTA[A/C]CAGCATCTTTAGAAA | 10451 |
rs143580386 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756627 | TGGCAAATATTATTT[C/T]GTTTCAAAGTCATTT | 10451 |
rs143581321 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945846 | AAAAAAAGAAAGAAA[A/G]AAAAGAAAAACAGTC | 10451 |
rs143589751 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107694705 | GATTCTAAGATTATA[C/G]TGATCTTCAGGGCCC | 10451 |
rs143605199 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107930160 | AAAATAATTGTACAT[G/T]TAATAACTAAAAGAG | 10451 |
rs143608449 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963916 | TGTCTGGCTTAACCC[A/T]CAAAGAGGCAGCTCC | 10451 |
rs143609531 | snp | C/G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107645979 | ACTTAAAAATCTCTA[C/G/T]GTAACTTCTCTCCAT | 10451 |
rs143618003 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780047 | TATATAGCAAAGCAG[G/T]TGAGACTGTGGGCGG | 10451 |
rs143631668 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107660553 | GAAGCTTTCACTTTA[C/T]ACCCATTTTCCCTTT | 10451 |
rs143654253 | in-del | -/AAAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720385 | AGACACTGTCTCAAA[-/AAAT]AATAAATAAATAAAT | 10451 |
rs143654589 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107741450 | GAGCAGTGCAGGGTG[A/G]GGAGGGTCATGCTCC | 10451 |
rs143655848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107784138 | GTAATACATAAAAGA[C/T]GCCCTTCACACCTCT | 10451 |
rs143664555 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107711914 | TGGTCTCAAACTCCT[A/G]ACCTCAGGTGATCTG | 10451 |
rs143668555 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107674677 | GTTGAAGTACTTAAC[C/T]TCTCAGAACTTTGGT | 10451 |
rs143694534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107742207 | GTAATATTTTGCCAC[A/G]CAATAAGAATGCCAC | 10451 |
rs143699125 | in-del | -/GT | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107864654 | ATAAGTAAATGTGTG[-/GT]GAGTACTAGCATCCC | 10451 |
rs143706336 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107680050 | TTGCAAATATTGTCT[A/G]TAAAGATTAATCACA | 10451 |
rs143711396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107639987 | TGGCAAGGATAAGAG[A/G]CACCTAAAACTCACA | 10451 |
rs143725990 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107936281 | GTGGAAAACCTCTTA[C/G]AAATTTGAGGAAAGT | 10451 |
rs143735308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923907 | CATCTATAAATCAGG[A/C]AACAGGCCCTTACCA | 10451 |
rs143738676 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107867621 | TCAGGGAGGAATCAC[C/T]GCAGAGCTCCCCCTT | 10451 |
rs143746974 | in-del | -/GAGG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107651550 | GTAAGGAAGGGAGGG[-/GAGG]AGGGAGGGAGGGAGG | 10451 |
rs143753260 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107813639 | CTCTTCTAGCTATTT[A/T]GAAAAATGTAATGCA | 10451 |
rs143771772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107877156 | GGTAATCAGCACATG[C/T]AGTTACTGCTTTCAC | 10451 |
rs143776122 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107869489 | TCTGTTAAGCACTTG[A/C]CATACACAATTTCAT | 10451 |
rs143776185 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107821872 | TCTCGTATAAAGAAA[C/G]TGATTTATTCCAAAG | 10451 |
rs143780778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707783 | AGATCATACATGGTC[C/T]GTGGCCTGTGGGGGT | 10451 |
rs143785163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592653 | CTCTCATGCAAACAA[A/G]GGAAAAAACCTAAGA | 10451 |
rs143789112 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107746009 | TGTCATGGATGCTGC[A/C]GGAGTTATTTTCTTT | 10451 |
rs143805721 | in-del | -/AC | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107853660 | TGATGACAAAGCAGG[-/AC]CACAGAAAGACCATC | 10451 |
rs143828492 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107750270 | AACTGAATGGTATAT[A/G]AGCCAAGTGTAAACT | 10451 |
rs143836526 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107904740 | TAAACTAAAAATGCA[C/T]AGAAGAAAAATTTCT | 10451 |
rs143842595 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728588 | ATGAGGACAGTCATA[C/T]GTATACGTATACGTA | 10451 |
rs143855648 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821171 | CATATCCTTAGAAGA[C/T]AAAATCCTGAAGACA | 10451 |
rs143858484 | in-del | -/A | 0.262519 | 0.249686 | intron-variant | VAV3 | GRCh38.p7 | 1:107951812 | TATTATCAAAAAGTC[-/A]AAAAAAAAAACATGC | 10451 |
rs143865570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744138 | AACAGGATAGTGCAT[C/T]CTGGTCCCAGAGTCC | 10451 |
rs143867729 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107648414 | CTATAAAATTTCATG[C/T]GTTACTTGAAAATCC | 10451 |
rs143883043 | snp | G/T | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107639174 | ATACAAAAAAAAACC[G/T]CAAAATGAATCATAA | 10451 |
rs143895510 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107908334 | GGCTATAGGTGGCTG[A/C]TATCATAGGTGGTGG | 10451 |
rs143916104 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107730834 | AAACTTTCATCTTTA[G/T]AAAACAACAGTAGGT | 10451 |
rs143961690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107595984 | TTACGTTTCTGCTGG[A/G]TTTTTGGACATAAAC | 10451 |
rs143972518 | snp | A/G | 0.110167 | 0.207236 | intron-variant | VAV3 | GRCh38.p7 | 1:107926046 | GCACTTTGGGAAGCC[A/G]AGGCGGGCAGATCAC | 10451 |
rs143983043 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107796431 | AAAAACAAGACATGT[A/G]TACTGGGGCCAATGT | 10451 |
rs143985981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107885406 | CTCTCCTCACCACAA[C/T]TTATTTTAAAAGTAC | 10451 |
rs144001454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815324 | TTGGGAGTTAGTGAG[G/T]GGAAAGGGATGTAGA | 10451 |
rs144004213 | in-del | -/ATGA | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591413 | TTTCAGGATAAAGGG[-/ATGA]ATGAATGAATGAATG | 10451 |
rs144005477 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910367 | GAAGACAATCACATA[A/C/T]TTTTCACTCCAAGAA | 10451 |
rs144018167 | snp | A/G | 6.62295e-05 | 0.00575416 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874945 | CAAATGCCTCGAAAA[A/G]TTCACTTTTCCTCAT | 10451 |
rs144030295 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107642196 | GTATGAGATAGGAGG[C/T]TGGCACAAGATACAG | 10451 |
rs144036439 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107719751 | GCTACTATAAAGACA[C/T]ATGAACACATATGTT | 10451 |
rs144040290 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107771672 | AATAAGATAAACAGT[A/G]TAAAGCACTTAGCAC | 10451 |
rs144041492 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107733388 | CTGGATGGAGAATGA[C/T]TTTGATGAGTTGACA | 10451 |
rs144060993 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107709659 | GGAGATAACTGAATC[A/G]TGGGGATGGTTTCCC | 10451 |
rs144062114 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107881358 | CCTCAGAATTATAAC[C/T]GTACCTCTCTCTGCC | 10451 |
rs144069652 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107956486 | AAACGTACACAAGCA[C/T]ATATGCTACAGTCAG | 10451 |
rs144086562 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107843537 | TGCGTGTGTGTGTGT[A/G]TATATATATATATTT | 10451 |
rs144092184 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107617176 | ACTTTTCATTTTCTA[G/T]CAAGCTTTCAAAGAC | 10451 |
rs144094956 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107883174 | TAATGTACTTTCATG[A/G]GTTATATGTAATTAT | 10451 |
rs144095212 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107764244 | GTTCTGGTCAATACA[C/T]ACCAATTGTTCAGGA | 10451 |
rs144101768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107666286 | GGCACTCATGAATAA[C/T]GAACAATGTTCTTAC | 10451 |
rs144106156 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107846389 | GAAGAAACTGCATAA[C/T]GACAGGATCAAATTT | 10451 |
rs144114266 | snp | A/C | 1.65529e-05 | 0.00287683 | intron-variant | VAV3 | GRCh38.p7 | 1:107768426 | CACAATTTTAGCTAG[A/C]ATATTTTTACTCACA | 10451 |
rs144114390 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107729168 | TCTAGTTTTTAAAAT[A/G]CACTGACAGCAACAG | 10451 |
rs144133824 | snp | A/C/T | 0.0123227 | 0.0777048 | intron-variant | VAV3 | GRCh38.p7 | 1:107731756 | TGGAAAGAAGTTGTA[A/C/T]GAAAGACTCAAGCAG | 10451 |
rs144140870 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107661631 | TCTCTCAATAAAAGT[C/T]TGTTAAATAAATGAA | 10451 |
rs144152562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107666271 | ACAGAACTGGCTACT[C/G]GCACTCATGAATAAC | 10451 |
rs144160775 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107614310 | GATGGATGTAGCAAA[C/T]GCAGGAAAATAAATT | 10451 |
rs144189947 | in-del | -/CTTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722838 | AGCCCTATTATCCTC[-/CTTT]TCTTTTTTTTTTTTT | 10451 |
rs144190530 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107920930 | CTCACATGTGTTATA[C/T]ACAAAATAAGCAAAT | 10451 |
rs144199915 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107882580 | TAAGGAATATAATAA[C/T]ATCAAGCTTCTCTCT | 10451 |
rs144212572 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107889911 | CACTGTGAACATTTG[A/T]CTCAAAGAAGTAAGA | 10451 |
rs144218854 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812666 | ACACCTACTAGAAAT[A/C]TACATCCAAGGTTTA | 10451 |
rs144231576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107618228 | GGTTGGGGACACCTA[C/T]GATAGAGAGATAACA | 10451 |
rs144234989 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107767126 | AGTGGTGTCCTGGTG[C/T]TAAGCTAACAATAAT | 10451 |
rs144236071 | snp | A/G | 8.46934e-05 | 0.00650688 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107705022 | ATGCATCTTGAAGTC[A/G]TGGAAATTGGAGTCT | 10451 |
rs144238953 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107845455 | GAGAATGAGTTTGAC[A/G]AATTGACAGAAGTAG | 10451 |
rs144257526 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590579 | CTGCATCCTGAACCA[C/T]TGAATATCCGCAGGT | 10451 |
rs144258993 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107815665 | AACTGCTTCTTTAAA[C/G]AAGATAGGATATTTG | 10451 |
rs144275569 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107739549 | GGCAACTGATGGTGC[C/T]GGCATGGATTCTGCA | 10451 |
rs144277614 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107706090 | GGCAGAAAATTAGAC[C/T]AGGATAAGTTAAAGA | 10451 |
rs144277684 | snp | A/G | 0.00114062 | 0.0238539 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874983 | GTCTCACAACAGGCC[A/G]TGAGAAATGTCCTTA | 10451 |
rs144286054 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107946246 | ATGGATTCAAGATAA[C/T]GAAGGCTGAGCACTA | 10451 |
rs144287526 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107622935 | GAAAGATGAACACAC[A/T]GTTTTTGGCATTATT | 10451 |
rs144300943 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107833984 | GTATCAGATCTCAAT[A/C]AACCATAACATACTT | 10451 |
rs144306934 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107731283 | AGGACAACAGCATCT[A/G]GCATTCATTGTACCC | 10451 |
rs144317651 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107709740 | TATAAGGGGCTGCCC[A/C]CTTCACTGGGCACTC | 10451 |
rs144329024 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107892331 | CTGAGTGCCCATTAC[A/G]TACTAGGTACCACTT | 10451 |
rs144332715 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107613539 | CATTTTCATATATAC[C/T]CAATTAGTGTCTTCC | 10451 |
rs144345978 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107672101 | GGTGAAACACTGCCT[C/T]TACTAAAAATACAAA | 10451 |
rs144363933 | snp | C/G | 0.0573587 | 0.15934 | intron-variant | VAV3 | GRCh38.p7 | 1:107582495 | TATACATGTGCCACG[C/G]TGGTGCGCTGCACCC | 10451 |
rs144370416 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107728537 | GGTTCCAATCGGGGA[C/T]TCTTTCTATTACACT | 10451 |
rs144378385 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107940697 | TGGATAAACCTTCAG[A/G]ACATTAAACTAAATA | 10451 |
rs144382987 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107862451 | ACATGGAAAGTGCCA[C/T]CCTCCTTTTCTAGGA | 10451 |
rs144392898 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895295 | GGTGTAGAAAACCAT[A/G]GCTAACATTTGTATT | 10451 |
rs144399030 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107781896 | AATACTAATAAATTT[A/G]TCAAAAATAACTAAT | 10451 |
rs144405584 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107891708 | GCCAGATGTGGTGGT[G/T]TATGCCTGTAATCCC | 10451 |
rs144405613 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107828095 | CAGTTTTGGTGAGTG[A/C]ATTTGAAGGGCTAAA | 10451 |
rs144411776 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107891793 | GCAGTGTGCGGAGAC[C/T]GCGCCATTGCAGTCC | 10451 |
rs144413027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107792868 | CTGGTTTGCAATTAA[A/G]TAGACTGTAAGGAAA | 10451 |
rs144422885 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107780811 | GTGAACCACTGTGCC[C/T]GGCCATAAAGTTTAT | 10451 |
rs144433159 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107902142 | ATATTAAGCATGCCT[C/T]AAACTAAGAAAGCTT | 10451 |
rs144438163 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786453 | AGGCTCTGTGCCTTA[A/G]TTCCCTTACCTACGA | 10451 |
rs144438657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107607731 | ATCTTTTGATACCCC[A/G]AAACATAGATTATTG | 10451 |
rs144439023 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107693325 | TCATCCAACATTCAA[A/G]TTTGTTTCCAAGTTG | 10451 |
rs144471891 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107899544 | TACACATTGAGGGAA[-/G]GTTTAAGAAACAAGG | 10451 |
rs144473105 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107681862 | AGATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 10451 |
rs144473570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790635 | TCATACAAAAGTACA[A/G]ATGTTTTCCAGTGTC | 10451 |
rs144478994 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107744386 | CTCAAAGAGTCTTTC[C/T]TCATTCAAGGGGGTA | 10451 |
rs144510685 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586871 | AATCACAGTAAATAG[A/C]TATAGTACATCAAAT | 10451 |
rs144513869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632654 | ATATTACTGGCTGCT[A/G]GCAAGCAAAATGATT | 10451 |
rs144513925 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107687814 | TTTTTGGATTTTTAA[A/C]GTAACTTTATTCTGA | 10451 |
rs144517396 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107887753 | CCCATACACCAACAC[A/G]ACCCCCTGCTCAGAT | 10451 |
rs144528878 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107956010 | GGGAACAACGGCATA[C/T]ATGCATGCAAATGGG | 10451 |
rs144531158 | in-del | -/GTATACACTAGTATACTCTGTATACTCGAGTATACAGA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107644926 | TGTATACACTAGTAT[lengthTooLong]GTATACACTAGTATA | 10451 |
rs144532210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107855032 | AGAAAACACACAAAA[A/G]CAAAAGCATGGAAGA | 10451 |
rs144535456 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107748225 | AATGTAGTTTTCCTT[A/G]ATTTCCCCTTTTGCT | 10451 |
rs144539753 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107775376 | ATGAGGTCAGGAGTT[C/T]GAGACCATCCTGGCT | 10451 |
rs144546513 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107684911 | CTATATAAACAACAT[C/T]GAACAACACAATTGA | 10451 |
rs144550048 | snp | A/C | 0.0260105 | 0.111035 | intron-variant | VAV3 | GRCh38.p7 | 1:107905521 | AGCCAATGCTAAAGA[A/C]CTCTGACATCTTAAA | 10451 |
rs144550390 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107871211 | TTTCTTAAGCAAAGA[A/G]GTTAACTAACAAGAT | 10451 |
rs144557102 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107671846 | AAAACGTAATTTCCT[A/G]TATATACAGAACATG | 10451 |
rs144567050 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107637495 | GGGCATGGTGACGTT[C/G]ACCTGTAATCCCAGC | 10451 |
rs144577192 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107622643 | TGGTTATTTATGAAC[A/G]ATTGGAAATTCTCCC | 10451 |
rs144596394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107841266 | TCCTCAACAAAGTTC[A/G]TATTCTGGTGTATTT | 10451 |
rs144611984 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107727723 | CCTTTGTGGGCTTTG[A/C]ACATTTAGACTTGTG | 10451 |
rs144613660 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107875250 | CTTACATTCTAATAT[A/G]AAAAGACAGACAAAA | 10451 |
rs144613851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794438 | TTTTGACCTAAATAC[A/G]TTAAATTTAATCAGC | 10451 |
rs144618062 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107791957 | AATGACAACCTACAT[C/T]TGAACCCAGCTTTCA | 10451 |
rs144632061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729839 | TTTACCATAACAAAC[A/G]ATAAAGAGTATTGTT | 10451 |
rs144638136 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107795549 | AGGAAAAAAAATGAA[C/T]GCCCTGTCAAAATAT | 10451 |
rs144646423 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107694137 | GTTTGTTAGTTACCA[A/C]AGAACAGCCTAACCT | 10451 |
rs144650572 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755193 | AGATTCAGACTGCTG[A/G]GAGAAGAGGCAGAGT | 10451 |
rs144660984 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107849963 | TGTGGCCAACACACA[C/T]ATGAAGAAAAGCTGA | 10451 |
rs144664311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912921 | CATCAAAACCACTTG[A/G]TACAGTGGTCATATC | 10451 |
rs144684736 | snp | A/G/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107611760 | GAACAGGTAACTGAG[A/G/T]CTGTTCCACCCTGGT | 10451 |
rs144687563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107644871 | CCACATGCCCATAAC[A/G]TGTAAAATTATATTT | 10451 |
rs144692382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107629897 | GTATGTGGAAAACAT[A/G]ACAGTCTACTACAAA | 10451 |
rs144693943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107758864 | AATTGCAATTCTTAA[A/G]TTATGTTCTAATATC | 10451 |
rs144713344 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107585404 | ATAATCCTATTAAAA[C/T]TTTAAAGACAGACCA | 10451 |
rs144716338 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107618052 | TAAAGGAAGTGCAAC[C/T]TAGATCCCTCACATG | 10451 |
rs144721948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900755 | TATGCTCAGTTAACC[A/G]AGGTTATTGCATCAC | 10451 |
rs144723624 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107649547 | CAGAGTGATTATTGA[C/G]ATGATCCCCTTGGCT | 10451 |
rs144725884 | snp | C/T | 0.00171541 | 0.0292363 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642660 | CTTTCAGAAGTTCAA[C/T]GGTATCCCCGGCCTG | 10451 |
rs144733602 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107725437 | AGTGAGAGGGACACT[A/G]TGGAACGTCTACACA | 10451 |
rs144746693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107789281 | CAAAGATCACTGCTT[A/C]CTGAATGTTGTCCGT | 10451 |
rs144750845 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107870028 | TACAATTTCTTTATC[C/T]ACATTGATTGACGGG | 10451 |
rs144751203 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | VAV3 | GRCh38.p7 | 1:107866588 | TTGGGAGGGAGAGGC[A/G]GGTGGATCACCTGAG | 10451 |
rs144771323 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107695204 | ACAAATTACTTAGAG[C/T]TTTGTAGGCCATATT | 10451 |
rs144786381 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107796329 | TACCCAACCAAGCTG[A/C]CCGGCTTCCAACTCC | 10451 |
rs144814042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107696895 | CCTCCAAATCCTAGG[C/T]CAGTCATGAAAAACT | 10451 |
rs144840221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923156 | TGCTCTGTGTCATTA[C/T]AAGTTAAATTGCCTT | 10451 |
rs144840304 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966547 | GGGAGTTTGGATAAT[C/T]TAATTGTATTATATT | 10451 |
rs144844817 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107935296 | ATATTGAGTTCTTCC[C/T]AAGATAAACCTCTAG | 10451 |
rs144861165 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107758342 | TTCCAGGCTGAGATG[A/G]GAGGATCACTTGAGT | 10451 |
rs144869440 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107604042 | ACTGTAATAATAAAA[A/G]GCCAAAATTCAATCT | 10451 |
rs144875096 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107915158 | TTTAAACTTAATCCA[A/G]TAGGCCCAAAATGTA | 10451 |
rs144885998 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | VAV3 | GRCh38.p7 | 1:107813048 | GAATGGCATGAACCC[A/G]GGAGGCAGAGCTGGC | 10451 |
rs144901669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632374 | AGCACTGCTCTGGTA[C/T]AGCCCCACTCAGGTA | 10451 |
rs144904501 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107608829 | ATGCAAACCCAACTA[C/G]TACTATATATTCCCA | 10451 |
rs144905878 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107713073 | AAAGTTTAGATAAAG[A/T]CTTATACTATCTATT | 10451 |
rs144924392 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587459 | TAGATGAATTTGTTT[A/G]TTTTTCAAGCAAGAG | 10451 |
rs144939801 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107924389 | CTCCAGTCGATATTA[C/T]GACAAAAAAAAAAAA | 10451 |
rs144942084 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107805581 | GTGTTATCTTGGAGA[G/T]GACTGAGTTTCCTTA | 10451 |
rs144943353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903135 | CATGGGAATGTGCTA[C/T]AGAGAAAAAATGAGG | 10451 |
rs144949057 | in-del | -/GGCACT | 0.067446 | 0.170804 | intron-variant | VAV3 | GRCh38.p7 | 1:107953802 | ATCTATTTTAAGACA[-/GGCACT]GGCACTCTGAAAACC | 10451 |
rs144949817 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107859575 | AAAAATATTTACTGA[A/G]TCCCTTCCACACTGA | 10451 |
rs144950429 | in-del | -/A | 0.0923359 | 0.194016 | intron-variant | VAV3 | GRCh38.p7 | 1:107712655 | AGTCTATTCAAAAAA[-/A]TAAAATGCTCATTTA | 10451 |
rs144957103 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107927500 | AGTGGGCTCTGGGGG[A/G]TCTCCAATTACAGGC | 10451 |
rs144957554 | snp | C/T | 0.000197984 | 0.0099475 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642692 | AGCTGTAAAGGGGGT[C/T]CTTCATGCAGAGCTG | 10451 |
rs144969020 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107702395 | GTGGGCACACAGGGC[A/C]AAACCATAGCATAAG | 10451 |
rs144971374 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107595727 | AGTGGCCAATGTATG[-/G]GTTTTAGAAATACTA | 10451 |
rs144987897 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107863052 | AAAACATATCTACTC[A/G]GTTGTAAAATATACA | 10451 |
rs144987943 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107814197 | AACTGCTGGATCACA[A/C]AATAGTTCTATTTTT | 10451 |
rs144988371 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107657246 | AGGCATGAGCCACCA[C/T]GCCCGGCCTCTGTAT | 10451 |
rs145006082 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107738331 | CACGTTGTGCACATG[C/T]ACCCTAGAACTTAAA | 10451 |
rs145027610 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107815873 | AAGTTTTCCAGACCC[A/G]TGGCGGGGTGTGGAG | 10451 |
rs145028939 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107708440 | ATTAATCAAATGTTC[A/C]CATTTCTTTTGCTTC | 10451 |
rs145059409 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107709937 | GAACAGACGAATACA[A/C]TATTTTTACAAAAAA | 10451 |
rs145060751 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107629408 | GAGTTACTAAGACTT[C/T]TTTATCACATATTGC | 10451 |
rs145062439 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107581797 | ATGTTCATGAGCAGA[A/T]GAAAATTTACTCAGT | 10451 |
rs145065132 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773160 | GCATTATTATTTAAT[A/C]CATTAAAGAGATGAG | 10451 |
rs145072414 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107878687 | CAAAATGTTAGGGTG[C/T]CCCATCATTACTGAG | 10451 |
rs145092143 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107936885 | TTCCCCGACCGATCT[G/T]GTGATTTGATACACA | 10451 |
rs145097153 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107667451 | ATGGGGTAGCAATGC[A/G]GGAAATATAATCCAA | 10451 |
rs145098992 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107712937 | AAATAGGTGGAAAGC[A/G]AGAGGAAGAATTTCG | 10451 |
rs145103212 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107776311 | AAGTCCCACACCTCA[A/C]AAAAGTGTACCTTCT | 10451 |
rs145103574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107711312 | AATCTCTTGAGACCC[C/T]GAGTGCAAAGATTTT | 10451 |
rs145108290 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107868139 | TCAAGCTCCTGTGGG[A/G]CTTTGAAGCAAGGCT | 10451 |
rs145124275 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107714285 | TCTTCCCTTAGAATT[A/G]CCAATTAAACATTAA | 10451 |
rs145131906 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107672473 | ATAAAATTATAAGTA[A/G]GTGTTTAATAAGTCA | 10451 |
rs145133216 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107633394 | TTTGCAAGCCACTTA[C/T]ACGCACCAAGATCTT | 10451 |
rs145134580 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107585084 | GATTGAGAATGCTAT[C/G]ATTAGACTTTAGGCT | 10451 |
rs145141064 | snp | A/C | 0.0228947 | 0.104514 | intron-variant | VAV3 | GRCh38.p7 | 1:107759987 | ATGCATTTTTAAGGA[A/C]TAATCAGGGTTTGAA | 10451 |
rs145149150 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107824294 | AGAAATTTTTCTGAG[A/C]AAGGGAAATGAGAAT | 10451 |
rs145153776 | snp | A/C/T | 0.00239393 | 0.0345281 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589411 | CAGCAGAGACTGGAG[A/C/T]GGTGCATCTATAAAC | 10451 |
rs145158149 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107587143 | TGTAACACTTGAGAC[A/G]TGAGTATGATATAGT | 10451 |
rs145189121 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107874611 | CAGCAGAAAAAAAAT[A/T]ATCTCTGGAGAAAAG | 10451 |
rs145199261 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107876605 | GCATGGTCAACTCAT[C/T]CACACTATAACAGGG | 10451 |
rs145245330 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107836945 | ACAAAAAAAAACAGG[C/T]GGATTCACAGCCAAA | 10451 |
rs145249945 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107929317 | AAAAAATTATGCCCT[A/G]GAACAGTATATTCAG | 10451 |
rs145252534 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107946909 | TTTATTAAGAGTTTA[C/T]AACATTCAAAGCTCT | 10451 |
rs145263679 | in-del | -/TT | 0.494896 | 0.0502606 | intron-variant | VAV3 | GRCh38.p7 | 1:107586140 | ACTCCCTTGGCATAG[-/TT]TTTTTTTTTTTTTTT | 10451 |
rs145266762 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107879558 | ATTACTTGAGTGTTT[C/T]TTTTTCCCAGTCTAT | 10451 |
rs145287532 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-5-prime | VAV3 | GRCh38.p7 | 1:107754795 | TGAGCATTTCACCTG[C/T]TACGGCTTCTGCCTG | 10451 |
rs145295125 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107816573 | TATTTCACTCCAATG[C/T]TAAATAGGCCTGCCT | 10451 |
rs145295365 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107680228 | TCACCAAAAAAAAAA[-/A]CCTCTCAACTATCAC | 10451 |
rs145305546 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107723049 | TCCACTATAGACTTC[A/G]TCATGTTATTGTGTA | 10451 |
rs145305659 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | VAV3 | GRCh38.p7 | 1:107761115 | ATTTTCTTGGCCGGG[C/T]GCGGTGGCTCACGCC | 10451 |
rs145311027 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107951070 | AATGCAAATGGTATG[A/G]CCAAATTTCCAGTAC | 10451 |
rs145313499 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107886438 | AGCCTTAGGACTGGA[C/T]TGCAGGCACCTGCCA | 10451 |
rs145331072 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107721291 | CTCATCCAAAGATAT[C/T]GGCTGCTACTGTATG | 10451 |
rs145337562 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107838929 | AAAGATGGGAACAAT[A/T]GGCACTGAGGACTAC | 10451 |
rs145344689 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107901350 | TTTAAATTTTCACCA[A/G]AAAAATCACAAGAAT | 10451 |
rs145345251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107644856 | GGACTGGAATGCCCA[C/T]CACATGCCCATAACA | 10451 |
rs145351393 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710428 | ATCGATTTATAAAAA[G/T]GTATTCACACACATA | 10451 |
rs145356281 | in-del | -/T | 0.314544 | 0.241524 | intron-variant | VAV3 | GRCh38.p7 | 1:107804761 | TTTTTGGTTTTTTTT[-/T]GTTTGTTTGTTTTGC | 10451 |
rs145357106 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107652074 | GGCTGCACTCCCAGA[C/T]GGTTAAGGCATTCTA | 10451 |
rs145358260 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107789695 | AATGTGTAAGTCACA[C/T]ACATAACTTAATATT | 10451 |
rs145366289 | in-del | -/ACAG | 0.277867 | 0.248442 | intron-variant | VAV3 | GRCh38.p7 | 1:107646212 | AGTGATTAATTGGAA[-/ACAG]ACAGTCATATTCCTT | 10451 |
rs145373414 | in-del | -/TC | 0.497803 | 0.033074 | intron-variant | VAV3 | GRCh38.p7 | 1:107701458 | GTCCACAAAACCATT[-/TC]TCTCTCCTAGGACTC | 10451 |
rs145375974 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107726077 | ATTATGCTATCAATA[C/T]CCCTATCTCAGAATT | 10451 |
rs145389046 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107840782 | TTTAAAAATAAAAGG[C/T]AAACTGTCTAGTTGG | 10451 |
rs145400046 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107793944 | TTGCGTACTGCTGGA[C/T]ACGCCAAATCCCAGA | 10451 |
rs145401761 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107773581 | ATGAGGAGAGGAACA[A/G]ACAGAGATAGGAGAC | 10451 |
rs145403388 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107785258 | CTGAGTTAAGAAAGG[-/C]CACAGCCACAGTAAC | 10451 |
rs145412437 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689580 | GAAGATCCATGGGCA[C/G]AAAGTCACCTTCAGA | 10451 |
rs145434286 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107604585 | TCTTGTCTGGAAACA[C/T]TCATACCCTATCAAC | 10451 |
rs145448971 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107727253 | GTTTGGGTTCTTTCG[C/T]AATTTTGTTCTCCTT | 10451 |
rs145452183 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107693659 | CATCCTATAACATCA[C/T]TAAAAATTATATTCT | 10451 |
rs145467336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107769337 | GAAGTTAAGCATGGA[C/T]ATTACCGATCGTCTA | 10451 |
rs145469457 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107675463 | TGTAGAACCCTCAGT[C/T]TATACCACCACACAG | 10451 |
rs145473043 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107609661 | ATAAGATACATATGC[A/G]TATGTTCCATTCCTT | 10451 |
rs145478916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107961815 | AAGATAATCAACTAA[C/T]TTATTAAGATTCCAA | 10451 |
rs145500872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107606997 | TCTCACACTGTCACC[C/T]GGGCTGGTGTGCAGT | 10451 |
rs145504620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657206 | GTGATCCGCCCGTCT[C/T]GGCCTCCCAAAGTGC | 10451 |
rs145507444 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107947829 | ATTCATTAAATAATC[A/C]CTCAATGACCATTCA | 10451 |
rs145509261 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107847133 | TCACTCAAAACCACA[C/T]GACTACAAGGAAACC | 10451 |
rs145510004 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107613386 | CTCCATTTTCTGTTT[C/T]ATTTTTAACTTCTTA | 10451 |
rs145513695 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897746 | TGAATGGCAGCCTGG[C/T]ATTCTGAGATTATAC | 10451 |
rs145523872 | in-del | -/TTTG | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107912046 | AAATACCAAGTGTTT[-/TTTG]TTTGTTTGTTTGTGT | 10451 |
rs145539109 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107732594 | GGGTCCCATGCCCAC[A/G]GAGCCTCGTTCACTG | 10451 |
rs145541457 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107611153 | AAATCTAAAATCGTA[C/T]GTGCTCCAATGAGCA | 10451 |
rs145543514 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107925379 | TGAATTTGTATACCC[A/G]TATTCAGAGCAGCAT | 10451 |
rs145555574 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107616034 | AGCCTTTGTGGAAAG[C/T]AGTGTGACAATTTCT | 10451 |
rs145566213 | in-del | -/GTGT/GTGTGTGTGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889132 | GTTCTCCTGTGTAGA[-/GTGT/GTGTGTGTGT]GTGTGTGTGTGTGTG | 10451 |
rs145571837 | snp | A/G | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966836 | TTTGGCAAATAAATC[A/G]TACTAATCTCTACAT | 10451 |
rs145606058 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107933055 | AAGGAATATATCTCC[C/T]CAATAAATATGCCTA | 10451 |
rs145615580 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107843064 | GTTCCTGAAGTCCAC[C/G]TTTACTCCGCCCTTC | 10451 |
rs145616180 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107887148 | CCAACCCAAGCCCCA[A/G]GCTGCACCCTTTACC | 10451 |
rs145629544 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107819686 | ATTTATGTAGGATTT[A/C]ATAATGCCTTTAAAA | 10451 |
rs145630045 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107892650 | ACTCCTCTCTATCTA[C/T]ATATAAAGACTACAA | 10451 |
rs145648808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774613 | AAAACAATCGACATG[A/T]AAGGCCACCTACATA | 10451 |
rs145654277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794537 | ATTTTGAGATTCCCT[C/T]CTCTCTTTCATTCTA | 10451 |
rs145661785 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | VAV3 | GRCh38.p7 | 1:107733980 | GTCAGGTTACCCACA[A/G]AGGAAAGCCCATCAG | 10451 |
rs145669023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777387 | ACCCTCACTAAATAT[A/G]TAAGTTGTCTGCTGC | 10451 |
rs145672414 | snp | A/C/T | 0.00398691 | 0.0444912 | intron-variant | VAV3 | GRCh38.p7 | 1:107728817 | AATGCAAGCCGAGGG[A/C/T]GCAACTATAGAATTA | 10451 |
rs145684748 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107863078 | ATACATAAATTAAGG[G/T]TAAATGCCATTAGAA | 10451 |
rs145701672 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107694219 | GGCTACCATTGGATG[A/G]TCAAGGTACGGTTAA | 10451 |
rs145704197 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107851936 | GTTTTACTAGATACA[A/G]TAAAATGGAAACATA | 10451 |
rs145707680 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107611090 | GTTTCACATTTTGGA[A/T]TTAAAAAAATTAGAA | 10451 |
rs145737755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858911 | TAGGCAGGGATAAAT[C/T]AGAATTCTAACATTT | 10451 |
rs145760320 | in-del | -/TGCTGG | 0.320814 | 0.239761 | intron-variant | VAV3 | GRCh38.p7 | 1:107806419 | TGAGTTCTGGGATAT[-/TGCTGG]TGTTAGTCTTGCTGC | 10451 |
rs145763544 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107736009 | AAAAGCTTATCCACC[A/G]AGATCAAGTTGGCTT | 10451 |
rs145786766 | snp | G/T | 0.0142736 | 0.0832652 | | | GRCh38.p7 | 1:107673780 | GCATTTAATAAACAT[G/T]TGGCTGCACATAAAA | 10451 |
rs145790268 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107857972 | TGCAGATTTTATTTA[C/T]GTAACAAGTAATATA | 10451 |
rs145794801 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107750913 | TCCTTCTTAATAACT[C/T]AGACAAACTAATAGA | 10451 |
rs145800880 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688828 | GACGATTTGTAACAA[C/T]AGCAAATTATACATA | 10451 |
rs145815490 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107620806 | GATGAATTTTTTAGC[A/T]GATGAAAGTGTATGG | 10451 |
rs145820217 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107639505 | TGGCTCATTAAAAAG[C/T]TGACAAAATATTTGA | 10451 |
rs145827868 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107624015 | GAGTCATCAAAATAC[A/G]TGACAAAGGCTTCAA | 10451 |
rs145830181 | snp | C/G | 0.111576 | 0.20818 | intron-variant | VAV3 | GRCh38.p7 | 1:107958714 | ACATGTGCCATGGTG[C/G]TTTCCTGCACCCATC | 10451 |
rs145831275 | in-del | -/ATTTT | 0.446641 | 0.154377 | intron-variant | VAV3 | GRCh38.p7 | 1:107631473 | ACTTTCTCTTTTTTA[-/ATTTT]ATTTTATTATTATTA | 10451 |
rs145840489 | in-del | -/AAC | 0.0279526 | 0.114869 | intron-variant | VAV3 | GRCh38.p7 | 1:107763380 | TCTGAAAGAAGGAAG[-/AAC]AACACTCAAACAAGA | 10451 |
rs145853823 | snp | C/T | 0.00358779 | 0.0422022 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570733 | ATTCGGGATCTGAAC[C/T]GGACTCCCTTTCGAT | 10451 |
rs145865021 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107628687 | AGTGTGTTTTTCTTA[A/G]AGGTGTTAGAAAATT | 10451 |
rs145893056 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107575672 | TCAACTGTGTGGTGA[C/T]CTTGCATAGGTCTCC | 10451 |
rs145912158 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897654 | TGCCCATGACACCAC[A/G]GTAACTCAGTAAGTG | 10451 |
rs145918701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107898721 | TATCTCCTATAAAAA[C/T]ATATCTACTGAAAAC | 10451 |
rs145924444 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107784619 | CATAAGCCGTGCCAG[C/T]GATCTGTTCATTGGT | 10451 |
rs145926469 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790680 | CCTTAAATGTCTTCC[-/T]TTTTTTTTTTTTTTT | 10451 |
rs145932574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107724086 | GAGTATAGAAATTAA[C/T]ATGTGAGTCATGAAG | 10451 |
rs145935421 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107788788 | TGTTAGTACACAACC[A/G]TAAAAGAAACACTTT | 10451 |
rs145944994 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686645 | TCCACACAAAACAGA[G/T]ATTTTTAGTACAGTC | 10451 |
rs145947076 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107601823 | TTTGATGTGATTTGA[C/T]AATATACTATTTCCA | 10451 |
rs145955870 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107692520 | CAATCTTCAGCTCAC[A/G]TAAAAGTACTGTGAT | 10451 |
rs145958740 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107607243 | AGGCACGAGTCAACA[A/C]GCCCAGCTGAGTCTG | 10451 |
rs145966163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868309 | GTTTACATATGTATA[C/T]ATGAAAAAATGTTTT | 10451 |
rs145970661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107961165 | TACATACACTGTCCA[C/T]AGTGGCCACTAAACT | 10451 |
rs145990462 | snp | A/G | 0.000399281 | 0.0141238 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964719 | TGATGGAGTGCGCCC[A/G]GAGGTTGTTAAGCAG | 10451 |
rs145995870 | snp | A/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107849252 | GCAACCAAAAAAAAA[A/T]AAAAGTCTGCATAGC | 10451 |
rs145998372 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787823 | GACTGCACTTGCCTC[A/G]TTAGGCATTTCCGCA | 10451 |
rs146003341 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107850410 | AAAAGAATGAGTTCA[C/T]GTCCTTTGCAGGGAC | 10451 |
rs146024475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914042 | TCAGGTGATCTGCCC[A/G]CCTTGGCCTCCCAAA | 10451 |
rs146036360 | in-del | -/TA | 0.0425829 | 0.139564 | intron-variant | VAV3 | GRCh38.p7 | 1:107642920 | TTTCAACTTTCTCAT[-/TA]TATGAGATGGTAATA | 10451 |
rs146044844 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107803225 | ATTTGGGCCTTCTCT[C/G]TTTTTTGGTAGTCTA | 10451 |
rs146048350 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107878819 | TGGTACCATGTGGCT[-/G]GTCCTATTTCCCAAT | 10451 |
rs146049333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107809803 | TCTCAAATAATCCAA[A/G]CATTATGACACTGAG | 10451 |
rs146052974 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107701131 | TGTTCATGTCCTTTG[C/T]CTGCTTTTTAATGGG | 10451 |
rs146064091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107704260 | TGGTTTTAGTCATTT[A/G]TTTAGGGCTTTTAAA | 10451 |
rs146070054 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107746965 | GCTCACTGCAACCTC[A/C]GCCTCTCAGGTTCAA | 10451 |
rs146083978 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572633 | GACACCCTCTCTTTT[A/G]TGTGCTTTTTTCACC | 10451 |
rs146084115 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624875 | GGACACAATCTTCAA[A/G]GATCTCATTCAGACA | 10451 |
rs146094500 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107578609 | CTCCTTGGACTGTTT[A/T]CTTTCTTTCTTTTTT | 10451 |
rs146114103 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107900036 | ATATCAGCAGGCATT[C/T]GTAGCTCACTAAAAT | 10451 |
rs146122959 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728618 | ATATGTATATGTATA[C/T]GTATATGTATATGTA | 10451 |
rs146124588 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107789208 | CAATCACACAGCTGG[A/G]ACAAAGTCAACACAT | 10451 |
rs146124612 | snp | A/G | 8.26139e-05 | 0.00642652 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642638 | CAAAACAGACTGTGT[A/G]CATCTCCTTTCAGAA | 10451 |
rs146150123 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107869146 | CCCCATTCCTGAACC[A/G]TCACTATGTGGTCAA | 10451 |
rs146152466 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107708337 | TTAACTCGCTCAGTC[-/A]ATGCTGATACACATA | 10451 |
rs146165527 | snp | A/G | 0.00152857 | 0.0276034 | intron-variant | VAV3 | GRCh38.p7 | 1:107749600 | GAAGATATGCCTGGG[A/G]AAAAGAGATTGATTG | 10451 |
rs146179354 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107690733 | TAGGAAAAATTGAAA[A/T]GGGGCTTTGTGCTGG | 10451 |
rs146203400 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107647879 | CAATCTAAGAATCAG[G/T]TCCTAAGAATCAGGT | 10451 |
rs146204324 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595163 | TTTTAACATAAAGTT[C/T]GCTCTACTTTCATTG | 10451 |
rs146216329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914530 | TTGAGGATTAAGTGA[A/G]CTAATGCCCATGAAA | 10451 |
rs146220262 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107718331 | TCAGCCCAAAATCTC[C/T]TTAAGATGATAAGCA | 10451 |
rs146223157 | in-del | -/CTC | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107632902 | ATTTCTCCTATGATT[-/CTC]CTAAGTGTCTCCAAA | 10451 |
rs146234937 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107881277 | CTCCAGGAGATTACA[C/T]GGAAAAGAAATATTT | 10451 |
rs146244286 | snp | A/C | 0.000460715 | 0.0151705 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964851 | TGAGCCACTGCGCGC[A/C]CTGCTTCCACGGCTC | 10451 |
rs146245342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107811171 | GTTTTTAATCACTTT[C/T]CACACTCAGAAAAAA | 10451 |
rs146260237 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107705349 | CACATAGGTCAACCT[A/G]CCTGGAAAAAAAAAA | 10451 |
rs146286550 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107815002 | GTATGAGAGAGCCCC[C/T]AAAAGTTCCTAGCCC | 10451 |
rs146286694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767985 | GGGAGTTACATATGA[C/T]ACAACTGGAAGTAGA | 10451 |
rs146290239 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107694339 | TAGTAAGAGCCAAGT[-/G]AGAACTCTAACAATT | 10451 |
rs146291452 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107692031 | CTTATCTGAAGTTCT[A/T]TTCAGACTAAACACA | 10451 |
rs146300709 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107708955 | CCACACACACATACC[A/C]CCCCACACACCCTAT | 10451 |
rs146310785 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107579764 | CTGAATTCCATGACA[A/G]TTCATAATCTGGCCA | 10451 |
rs146312330 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107665305 | ACAACAAGGGGTGCA[C/T]TGTCTGGGGATAATT | 10451 |
rs146334914 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107942178 | CTGCAAATGCAACTT[C/T]TCTGTAACCACTTGA | 10451 |
rs146354562 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | VAV3 | GRCh38.p7 | 1:107892130 | TTTTATGTGATTAAT[A/G]TGTCATAATGGCATG | 10451 |
rs146360574 | in-del | -/ATAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107843380 | ATATATATATATATA[-/ATAT]TATATATATAGTTAA | 10451 |
rs146404934 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107720826 | GAGGTGAGAACTTGA[A/G]CAGGACTTGGGGAGC | 10451 |
rs146407666 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786025 | TTCCTGAAGCACCTG[C/T]TTGTTGCTTTGATCT | 10451 |
rs146407755 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107837203 | CAACTCTAGAAGCAC[A/T]TCAAAAAGTTAGTTT | 10451 |
rs146412674 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879599 | AGATTAGAAGTTATC[A/T]GCTAGACCTTTGAAT | 10451 |
rs146416445 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107681717 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 10451 |
rs146419155 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107596099 | AGAAGTCCTTGCTCA[C/T]GCATTAGCGCATCCA | 10451 |
rs146446702 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107881360 | TCAGAATTATAACTG[C/T]ACCTCTCTCTGCCTT | 10451 |
rs146451156 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107956750 | CCCACTTGAGGTTAG[A/G]GATCATGAACTTAAA | 10451 |
rs146453029 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107840813 | CAACAGACCAAGATA[C/T]AAGTACAGCATATTT | 10451 |
rs146456950 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107640948 | TCAAAAGCCAGCTGA[G/T]GGAATACGGGATAAA | 10451 |
rs146464618 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107843614 | TGAAGTATGAGCAGG[C/T]GTATTTAAACCTCCA | 10451 |
rs146475857 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107729684 | CCATCATAATTTTGT[A/G]ATTATTTAACAAGAT | 10451 |
rs146485926 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107732339 | TACAACTGAGGTACC[C/T]GGTTCATCTCACTGG | 10451 |
rs146500892 | in-del | -/CTCT | 0.105214 | 0.203807 | intron-variant | VAV3 | GRCh38.p7 | 1:107907688 | TCACACACACACGCG[-/CTCT]CTCTCTCTCTCTCAT | 10451 |
rs146504994 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107614901 | TTCTTGATTTGATGT[A/C]TTTAGGTTCCCAAAC | 10451 |
rs146530305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698164 | TGAGTTAACAATGGT[A/G]AAGTACAAATGGTCC | 10451 |
rs146536056 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107890255 | ATATATTGTTATCTG[C/T]ATGTTTACACATACA | 10451 |
rs146546485 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618768 | TGTTCTAACTTCAGG[A/G]CTCTGCACTGCCTCT | 10451 |
rs146564221 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107845503 | ATAAAAAACTCCTGC[A/G]AACTAAAGAAGTATG | 10451 |
rs146576633 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107892369 | ACGCTGAGTACAAGA[C/T]TAGATGCTAAAGATA | 10451 |
rs146577235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107859071 | TGAAAGATTCTTGAG[A/G]AGTTTTTTTTTTTTT | 10451 |
rs146581069 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV3 | GRCh38.p7 | 1:107862737 | CAGCTCAGATAGGAT[A/G]CGGCCCAACAACTAA | 10451 |
rs146586778 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782696 | AGCAAATAAAGACTG[A/T]TTAGTCAATGCGGTG | 10451 |
rs146597352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107740554 | GAGTTAAAAAACATT[C/T]TGGAGCTAAATCATC | 10451 |
rs146597676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786466 | TAGTTCCCTTACCTA[C/T]GAAATTACAATTAAA | 10451 |
rs146603313 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107677506 | CAACCAGCATAACCA[C/T]AGATATGGCAAAGGA | 10451 |
rs146608213 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107744807 | GTTTTAGATGCCAAG[A/G]TCTGAGTCCAGTTGC | 10451 |
rs146619928 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107812439 | TTTTATTTATTATCA[-/T]TTTTTAAGCTGATTT | 10451 |
rs146624629 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107632688 | CTAAAGACAGGAGAC[C/T]TAATGTCAAACCAAT | 10451 |
rs146670104 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107916744 | ACCTATAACTAGAAC[A/G]AGTGTCTAGAATCAC | 10451 |
rs146675205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880471 | AGATCTTGGCTTTGT[C/T]CTAGAAGTGATGAGG | 10451 |
rs146676055 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107907359 | ATTCAAAAAGATGTT[A/G]ACAATATCGTAAGTG | 10451 |
rs146694856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910637 | TGTAATACTAATAAC[A/G]TAAGGTTTTCTTCTC | 10451 |
rs146697998 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107879236 | TCTTATTTTCATTTA[C/T]ACAATAAATAGTATT | 10451 |
rs146704905 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107798810 | CTGCTATGAAATTGC[A/G]CTTTTCTATTGATTT | 10451 |
rs146716805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804490 | AGAGATGACAACTTA[C/T]CACAGATCACCCCAA | 10451 |
rs146717004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107760977 | ACAATAAATGAGTGC[A/G]TTTGTTTCCTTAACA | 10451 |
rs146720455 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107698486 | TAATGTACAATAGGT[C/T]AGGTGCATTGAATGC | 10451 |
rs146727924 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107763049 | AAAAATAACCACAAA[A/G]CAGAAGACACAAAGA | 10451 |
rs146742823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656887 | AACTTCTGACCTCAG[C/T]ATATACAACAACACA | 10451 |
rs146750974 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107745405 | AAAGCGGGGGGGAAT[-/C]CCTCCTGCCGTATCC | 10451 |
rs146784491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107573833 | CCCACTTGCCCAGGT[A/G]AATTTTATTTATGTC | 10451 |
rs146785969 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107660824 | GAAAATTATACAGGC[A/C]AATATTACAAAGCAT | 10451 |
rs146814569 | snp | C/G | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107936757 | AAGAAGTTGTCAGGA[C/G]CATAAGGATGTCCTG | 10451 |
rs146818085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807523 | AAGCCAGAAACAAGA[C/G]CAGGGTCGTAGTGCT | 10451 |
rs146818889 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107889345 | AGTTGCCACGCAAGG[C/T]TTAACACAGAAATGT | 10451 |
rs146838424 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107828345 | GGCCTGAGGTCTAGG[C/T]CTGGCTTATCCTCTA | 10451 |
rs146842692 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107714691 | GAAAGGGCAAGAAAA[C/T]GAAAAACAAACGGGT | 10451 |
rs146849853 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107781738 | GAAACCCTTCATGCA[A/G]TTTCTTCCTGGTCAA | 10451 |
rs146854067 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107673666 | CTTAACACCAAGTCA[C/G]TATACTTGTCAAAGA | 10451 |
rs146864111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592031 | ACAAAATATGTTACT[A/G]TACACACACACATAT | 10451 |
rs146879569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702898 | TCAACATTATCTCAC[C/T]GTATCCTCATAATAA | 10451 |
rs146885437 | snp | C/T | 1.65334e-05 | 0.00287514 | missense, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107751136 | CTTGTTTGGTATGCT[C/T]GTCTAGAGTGGTTAT | 10451 |
rs146890797 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676163 | ATTCATTTGTAAACA[G/T]AATTATAGAAAAAAA | 10451 |
rs146893891 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107766046 | CATAAAATACCAGAA[C/T]TGGAAGAAAAGTGGA | 10451 |
rs146896255 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | VAV3 | GRCh38.p7 | 1:107848308 | ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA | 10451 |
rs146929171 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107707369 | CAGCGTGATCTTAGG[C/T]AAGTTAGTGAGTATA | 10451 |
rs146930915 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107769602 | ATGGCCCAATCTATT[G/T]GTCAATTCAGTCTTT | 10451 |
rs146939114 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107663087 | ACATTCTTGTATAAA[C/T]CAAAAAACGTATTTA | 10451 |
rs146941115 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107576650 | CAGAGCTGTCTATCC[C/T]TTTACAGGCAAACAC | 10451 |
rs146968047 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107938595 | CAGAAGTGCCCAGTG[A/G]ATGACTTGGTTGTCC | 10451 |
rs146971491 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107944300 | TAGCTTGTCATAAAA[A/C]TGAGAATAGACTGTA | 10451 |
rs146980332 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107825527 | ATGTAGGCAGGCTCA[C/T]GATAGAGAAAAATCT | 10451 |
rs146988156 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107893331 | TTTCCCAAAAGTACC[C/G]ATCTCCAACTTTATA | 10451 |
rs146990104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107830705 | GCCTTTCTTTACCTA[C/T]GATTGTCTTGGTAAA | 10451 |
rs146998494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719574 | ACAAGTGCTGGAGAG[C/T]ATGTGGAGAAATAGG | 10451 |
rs147013245 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593082 | CATTCCAAAGACAAA[G/T]ATAAAATCCCATCAC | 10451 |
rs147021937 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856533 | CAGGACCGAAATATT[-/A]AAAAAAAAATCAACA | 10451 |
rs147030000 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787442 | AGCCCAGGGGAGACA[A/G]CAAGGCCAGTTGCAC | 10451 |
rs147033067 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107679640 | AAATAAATCTTGTAT[A/C]TCCTACACTGAGACA | 10451 |
rs147034362 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107722047 | TGGGCTGGACTTTAT[C/T]CTGGTGGTTAGTATC | 10451 |
rs147043041 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107682128 | TTTATTGTTGTTCTA[C/T]TTTGCCATATTTCTA | 10451 |
rs147048640 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107598964 | AGCTTTGAACTTCAA[C/T]GTAATTTTGTTATAG | 10451 |
rs147072283 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107958827 | GTTCCCCTCCCTGTG[C/T]CCATATGTTCTCATT | 10451 |
rs147074948 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107882197 | AGAAGGTCGGTGAGT[C/G]CTAATAGACCTTCAC | 10451 |
rs147075336 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962997 | TATAATGACAATCTT[C/T]GGTCATCAGAAAGAT | 10451 |
rs147078178 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107884738 | TATAAGCATAAGCAT[C/G]ATGCCTGGCCCAAAA | 10451 |
rs147078891 | snp | G/T | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107844421 | ACTGAGTTAGCTGCA[G/T]AAGTTTTTTTTCCGT | 10451 |
rs147082826 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107766749 | AGGGGAGGAAGCAGC[A/G]GGAGAGGACAGGGTA | 10451 |
rs147088644 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107848695 | CTCTCACCACTCCTA[C/T]TCAAAGCAATATTGG | 10451 |
rs147092489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107769894 | GACCACCTATACCAC[C/T]ATTTTTGTCATCTCG | 10451 |
rs147106447 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107663761 | AATACTCTACTGCAG[A/C]TACTTATGGATCTTA | 10451 |
rs147133127 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107888340 | CAGATCAGCAAAACA[C/T]GTAGCGCTAGACTAG | 10451 |
rs147141448 | snp | C/G | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107776316 | CCACACCTCACAAAA[C/G]TGTACCTTCTAATGA | 10451 |
rs147162440 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107891734 | ATCCCAGCTACTTGG[A/G]AGGTTGAGGCAGGAG | 10451 |
rs147163863 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107856258 | AAATGTGATTAATTA[C/T]GGTTTACATCATTCC | 10451 |
rs147167244 | in-del | -/TT | 0.256897 | 0.249905 | intron-variant | VAV3 | GRCh38.p7 | 1:107681655 | TACGTAATGGAAAAC[-/TT]TTTTTTTTTTTTTTT | 10451 |
rs147173802 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107860858 | CAACACAGTGAGACC[C/T]TATCTTTTACAAAAA | 10451 |
rs147178474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780136 | CTTTTGGGCAAAATA[C/T]TTAACTTCTCTGAGC | 10451 |
rs147191351 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107674714 | TGCTGAAAAACCCCA[A/G]TGATCCTTGCCTCCT | 10451 |
rs147198281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107742295 | AAAATTTCAAATTTA[C/T]AACAAAAATATGATA | 10451 |
rs147200913 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625585 | AATTTAATCTGATAG[C/G]ATTTATTTACAGAAG | 10451 |
rs147201308 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107680236 | TTTCACCAAAAAAAA[A/C]ACCTCTCAACTATCA | 10451 |
rs147211506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107630831 | AGTACATGATTCCAC[A/T]TTTAGACCCAATAAG | 10451 |
rs147213341 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959270 | TGTCTAAAAAATAAA[A/T]AAATTAATTAATTAA | 10451 |
rs147217516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107951299 | TGTACTTTTGCACCA[A/G]TCTTATAACATCCAA | 10451 |
rs147237869 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107904765 | ATTTCTCTACCATCA[C/T]GAGACTTTCTCTTTT | 10451 |
rs147247778 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107794031 | CTGCGCAGAAGGCGC[C/T]TCACAGGGAGGATTA | 10451 |
rs147267627 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107909625 | AATTTCCGAAAAACT[A/T]ATGGTGTAATCTTAT | 10451 |
rs147267957 | in-del | -/TATATC | 0.321292 | 0.23962 | intron-variant | VAV3 | GRCh38.p7 | 1:107810462 | TCCACATACTCTATT[-/TATATC]TATAACTAAAGAAAT | 10451 |
rs147284385 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107877393 | AATTGCACACACCAC[G/T]CTCTGAAGATTTCCC | 10451 |
rs147284715 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107796651 | AAATAAGGATCAAAT[A/G]TTTGTAAGAGTACTT | 10451 |
rs147293289 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107697373 | GGAAAGAACTTAAAA[G/T]AAGGAGAGAGGGAGA | 10451 |
rs147303546 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649230 | GCTCATCTGACTACA[C/G/T]CCAAGTAATTCAGGG | 10451 |
rs147313429 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107654615 | GACCTTCCTTCCTTT[C/T]TCCCTCACTTTATCC | 10451 |
rs147326269 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571277 | GACAAAGTATATGGA[A/G]AACATTTACTTCTGT | 10451 |
rs147343971 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107927367 | AGACTCACGACATTC[C/T]CAGCTGTGGTGGCTA | 10451 |
rs147345315 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107861488 | ATTTTGGTAAAGAAT[A/C]CTTGTTAAACTTTAT | 10451 |
rs147352630 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107739613 | CATGCAAGCATTTTA[A/C]GGAGGAAGAATGTGA | 10451 |
rs147354873 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107815677 | AAAGAAGATAGGATA[C/T]TTGGAATGAAATTCA | 10451 |
rs147355290 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | VAV3 | GRCh38.p7 | 1:107864492 | GCTGGCTGTGGTGGC[A/G]TGCACCTGTAGTCCC | 10451 |
rs147388734 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107743009 | GACCAGGCCTGGCAG[A/G]GAAAGCTTATGTGTG | 10451 |
rs147391418 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107820388 | TTCACATGTTCTCAC[C/T]CATCTGTGGGAGCTA | 10451 |
rs147396719 | in-del | -/AAAAC | 0.168785 | 0.236441 | intron-variant | VAV3 | GRCh38.p7 | 1:107682710 | ACCACTTATGATAGG[-/AAAAC]AAAACAAAATGAAAC | 10451 |
rs147398417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107712749 | AAATAAGTAAAGTCC[C/T]TGACTAATGTTGGCT | 10451 |
rs147408186 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107715906 | CACATTTCAAATTAT[A/G]TCTGATAATATAAAG | 10451 |
rs147414538 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107586925 | ACTTAATTTGTTCAG[A/C]AAATAGGGTGTTTTG | 10451 |
rs147424304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590845 | GCATGCTTATCCCTC[C/T]CACGGACATCTGCAA | 10451 |
rs147448860 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107950483 | GGATTTGGAGCGTTG[A/G]AACATGACCAGGGGA | 10451 |
rs147450760 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107878207 | ACAGATAACACTTGA[C/T]TCCTAAATACTCTGA | 10451 |
rs147456645 | in-del | -/ACAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908821 | CCCCGCCCCACTCAA[-/ACAC]ACACACACACACACA | 10451 |
rs147458924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107758885 | TTCTAATATCTAATC[C/T]CATTAGAAATATTAT | 10451 |
rs147480068 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107880655 | ACAAAGATTAGCTGG[C/G]TGTGGTGGCACACAC | 10451 |
rs147480391 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107838213 | GCAAACTATGCATCC[A/G]ACAAAGCTCTAATAG | 10451 |
rs147486631 | in-del | -/T | 0.239326 | 0.249772 | intron-variant | VAV3 | GRCh38.p7 | 1:107909348 | ATATAAGTAAAAAAA[-/T]GTTATATGAGTATTT | 10451 |
rs147494677 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107761856 | TGACTTTAAAACTTT[A/G]CTCAAGTATAAACCT | 10451 |
rs147510293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655760 | AAACAACTAAGAAGA[A/T]ACAAATAATCTAATT | 10451 |
rs147514752 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107730554 | AAAGTGATCAAAAAA[C/T]CTTGAAATAAATTAA | 10451 |
rs147519400 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107608941 | TCTTTTTAAGAGAAG[C/T]CAAACACAAAATTCA | 10451 |
rs147529398 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107613137 | AGCTGGGTCTAATAA[A/T]CAACCTTTTATAGAT | 10451 |
rs147549661 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107851757 | TAATGTCACCATTAG[A/G]CAGCATCAGCTAAAT | 10451 |
rs147553617 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107773266 | CAAGTCTGTCTTAAC[A/G]CTGAGTGTTTTACCC | 10451 |
rs147563263 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107735663 | CTAAACTAGGAAGAC[A/G]CTGAATTCCTGAATA | 10451 |
rs147568705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667526 | CAAAATAATGTAAAT[A/G]AATTTATGATAAGGT | 10451 |
rs147574566 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107888005 | TCTATCCAAAAATTT[-/G]GGGGGGGGGGTTATT | 10451 |
rs147577259 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673003 | AAATCTAGGAGTTCA[C/T]ATGCTTTGACCCAGA | 10451 |
rs147577639 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107620120 | TTAATAGACTGTGAG[C/T]TCCTTGGCATAAGGG | 10451 |
rs147599513 | snp | C/T | 0.0622301 | 0.165053 | intron-variant | VAV3 | GRCh38.p7 | 1:107736957 | TGACTTCAAGCTATC[C/T]TACAAGGCTACAGTA | 10451 |
rs147613861 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107622815 | GTGTTTGGGGAAAGA[A/T]GATGTACAGCATGGC | 10451 |
rs147623730 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107947088 | TTGAACTCTAGAGCC[C/T]ATAACCTTTTTGCTA | 10451 |
rs147640095 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107835687 | GTCAATGGAGAGCAA[C/G]CTGGAGGTCCCCACA | 10451 |
rs147649781 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787475 | CTTCGTGGGCAGAGG[A/G]AGCTAGAGGGGTTCA | 10451 |
rs147649786 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107839143 | GAATACTGTAGTAGT[A/C]AAATGCATAAGTTAG | 10451 |
rs147654131 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107722059 | TATTCTGGTGGTTAG[C/T]ATCTGGGTATCCAAA | 10451 |
rs147659364 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107789963 | AACCATACTGAGTGG[C/T]ACAAGTCTACACAAA | 10451 |
rs147671894 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107604795 | TATAGTTTTAAAAGT[C/T]CATTCACATTATAAT | 10451 |
rs147672829 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689810 | AGAGCGCTGGTTTGG[A/G]AAGAGGTTCTATAAA | 10451 |
rs147682738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107693856 | TGTTTCATTACATTG[C/T]CCAGCTTCCCTTGCA | 10451 |
rs147699062 | in-del | -/GCACACGCGCGCGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575015 | TGCGCGCGCGCGCGC[-/GCACACGCGCGCGT]GTTTAATATTCGATG | 10451 |
rs147711502 | in-del | -/TC | 0.384785 | 0.210554 | intron-variant | VAV3 | GRCh38.p7 | 1:107885258 | TCTGTCGCTTTTATT[-/TC]TTTTATTTTTATTTT | 10451 |
rs147744038 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107916228 | AAAACTTCCTGGTAA[A/G]TTCAAGTGACATCAA | 10451 |
rs147752614 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | VAV3 | GRCh38.p7 | 1:107736084 | ACATAATTCATCACA[C/T]AAACAGAATCAAAGA | 10451 |
rs147753972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107806575 | GTTGGAATATTTGGT[A/G]CAATTTTTCTTGCTG | 10451 |
rs147762141 | snp | C/T | 0.199873 | 0.244923 | intron-variant | VAV3 | GRCh38.p7 | 1:107737482 | ACTAATATCCAGAAT[C/T]TACAAAGAACTCAAA | 10451 |
rs147772674 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107706619 | TATAAGGATCTAGAA[A/C]CAAAACTTTCTTCAC | 10451 |
rs147775555 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107622999 | AAAAAACCAGCAAAG[A/G]GGAAGTGATCAGGAA | 10451 |
rs147784989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107575922 | TGCCCATGCACAAAC[C/T]GAAGAACTGCAGAAT | 10451 |
rs147809038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709799 | AAAGGACGTGTTTGT[C/T]TCCCCTTCTACCATG | 10451 |
rs147813582 | snp | A/G | 1.64751e-05 | 0.00287007 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574140 | GGACAACTCTCTCAT[A/G]TCTCTTGCACAGAAG | 10451 |
rs147843994 | snp | C/G/T | 0.00637247 | 0.0561273 | intron-variant | VAV3 | GRCh38.p7 | 1:107871335 | GTCCCCCATTCCCCC[C/G/T]CTCTCCCCCCACCAG | 10451 |
rs147848627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943517 | AGGCCGAGGCAGGCA[C/T]ACACATCACGAGGTC | 10451 |
rs147851232 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107946652 | AAGGACTGAAAATAA[C/T]CCAAATAACTGATTC | 10451 |
rs147859859 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107830109 | TTTAAAGGCCATTGT[C/G]AGAAAAGTCTGAGAA | 10451 |
rs147860345 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107875366 | GGGATCAGGAGAGTT[C/G]GTGGGGCTGGGTGGG | 10451 |
rs147869973 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | VAV3 | GRCh38.p7 | 1:107834640 | AACTAGATGCAGCCA[A/G]GAAGCCCCTCTCCCA | 10451 |
rs147878271 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107721607 | GTGCTTTCAACCCAA[C/G]AGCAGATGGGTAGAA | 10451 |
rs147882740 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107645414 | TGATCTGTTGTCAGG[G/T]GTACAGAGATCAAAG | 10451 |
rs147892788 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107649679 | TCATAAAGGATATCT[A/G]AAGGAGAAGATAACA | 10451 |
rs147893457 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107598575 | CTTGTTGAAGCAAGA[A/C]ATTTGTAATCAGACC | 10451 |
rs147909683 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107916967 | GATGTAAAGTGTGAA[A/G]GCAGTGACTGGAAAT | 10451 |
rs147914739 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107725503 | GAAGAGCTGGTTATG[C/G]TAGGCAAATTCATCA | 10451 |
rs147916826 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964738 | GTTGTTAAGCAGCTG[A/G]CAGAGCAGGACTCCA | 10451 |
rs147929423 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107604317 | TTCAGCAAAAGTTTG[C/T]TGATGGAGGACATGT | 10451 |
rs147940119 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107923573 | TGGCTGAGGAGGCCT[C/G]AGGAAACTTACAATC | 10451 |
rs147964427 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107769607 | CCAATCTATTTGTCA[A/G]TTCAGTCTTTCCCCT | 10451 |
rs147972199 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107732820 | GCAGAAACGTTTGCA[A/G]ACTAAAATGTCCCTG | 10451 |
rs147982029 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699523 | CATTGTGGAATCTGG[A/C]GGACCGTGGCCCTCT | 10451 |
rs147987463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107616804 | GAAATATAGCAAGCA[C/T]GATAGATTAAGGAGA | 10451 |
rs147989626 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107898129 | GGAAGCAGATCAAAA[C/T]TCAGCACCTGTTCTA | 10451 |
rs147993690 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764076 | GAACTCCTCTTCAGG[-/AA]AAAAAAAAACAAAAA | 10451 |
rs148002508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868503 | GGTAGTAGTAAACCA[C/T]TGCAGGCTCTCAAGT | 10451 |
rs148007194 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788624 | TACCATCCCCCGGTC[C/T]AAATAGCAAAGTAGA | 10451 |
rs148015495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107685136 | CATGTAGGAACTATA[A/C]ACTTAAAATGTGAAA | 10451 |
rs148017342 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107748443 | CAGTGGAACTAAAAG[C/G]CACTTAAAGAAATCA | 10451 |
rs148054612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864039 | ATACCCAGGTTTAAA[A/G]GCCTCTGCAGAAGAG | 10451 |
rs148064254 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107819713 | AAAAATATATACACC[A/G]CCAAATACTCTTCCT | 10451 |
rs148064570 | in-del | -/A | 0.0711525 | 0.174681 | intron-variant | VAV3 | GRCh38.p7 | 1:107639162 | CTTAGTACCATATAC[-/A]AAAAAAAAACCTCAA | 10451 |
rs148071788 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107646163 | GCAAAGTAGCGTAAA[C/G]TACAAAACTTGAACT | 10451 |
rs148082073 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107630105 | TATCTATAGGTTTAA[C/T]GCTAGATATATTTGC | 10451 |
rs148092617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586198 | ATAATACACTTAATT[A/G]TTTTTCTAAATCCAT | 10451 |
rs148094975 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107880712 | GAGGCATGATAATCC[C/T]TTGAACCTGGGAAAT | 10451 |
rs148123235 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107814175 | TAAATACCCAGTCAG[C/T]AGCGAAAACTGCTGG | 10451 |
rs148130328 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107707864 | GATTGCAGCAGAAGA[C/T]GACAGAAATGTCAGG | 10451 |
rs148133071 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107770150 | CTGAACACTTTCCAA[C/T]CAGAGGGGCTCTCTC | 10451 |
rs148138578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592759 | CAGGCTAAGTGACTC[A/G]CCTAAGGTCAGACAG | 10451 |
rs148140579 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107664486 | ATTTTCAAAGTATAA[A/G]AAGCAGCAGCATAGG | 10451 |
rs148146742 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107577827 | GGGAAAGAGAAATAA[C/T]TATCTTCTTGAAGCC | 10451 |
rs148149012 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107877329 | CTCTCTTGCAATATC[A/G]TTTACATAATTAAGT | 10451 |
rs148152945 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107949943 | CTATATGATTAAAAG[A/G]AAGTTGTACTACTGA | 10451 |
rs148161365 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107837322 | TAAAATCAAAAACCA[C/T]ACGATCATCTCAATA | 10451 |
rs148165481 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107758385 | GATCAGCCTGGGCAA[A/C]ATGACAAGACCCCAT | 10451 |
rs148194816 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107657546 | TTGACGTTTTGTCCC[A/G]AGAGTTGCCTCTGGG | 10451 |
rs148196828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107730122 | ATTTTAATAAGTGAC[A/G]GGTCAAACACATGGT | 10451 |
rs148200968 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | VAV3 | GRCh38.p7 | 1:107944849 | GAGCTCTGGCAATCC[A/G]CCCGCCTCGGCCTCC | 10451 |
rs148209068 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107927147 | CACAGTCATGAGCCC[C/T]TTCCAGGCCCTAGCT | 10451 |
rs148213914 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107831894 | ATTAGGTATGTAAAA[C/T]TGCACCACATTTGGA | 10451 |
rs148223556 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107784993 | AACCAATGATGATTT[G/T]TATTTTGTTTTAGCT | 10451 |
rs148227894 | snp | C/G | 0.235273 | 0.249566 | intron-variant | VAV3 | GRCh38.p7 | 1:107719939 | CTGGAAACCATCATT[C/G]TGAGCAAACTATCAC | 10451 |
rs148231553 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | VAV3 | GRCh38.p7 | 1:107612098 | AGTTTTTAAAAAACA[C/T]TTTATTGAGAATATA | 10451 |
rs148254747 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107937521 | CCTCTACTATTTGAG[A/G]TAAGTACAAAACATT | 10451 |
rs148270999 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107890815 | CTACCAAAAATGGAA[A/G]ACACTTTCAGATCAT | 10451 |
rs148276832 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107959630 | CCATCTCTCTGCCCT[C/T]GAGAACAGGCATGCT | 10451 |
rs148281930 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107778362 | AAAAATTTTGACTTA[C/T]GTTTTTTCAGAATCA | 10451 |
rs148285393 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107691139 | CCTTTATAAACACAA[C/T]CTAAACTGTCATACC | 10451 |
rs148290520 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107674257 | TTCTGCTGGGTGTCA[C/T]ACACATGGCGTGTTT | 10451 |
rs148298501 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107666961 | GTTTCTGTATCATTG[A/G]TTTTCAAAAAGGCAT | 10451 |
rs148300385 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107624894 | CTCATTCAGACAATG[C/T]CATTTCCTTAATTCA | 10451 |
rs148329276 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107853628 | CTTTTAATGTCTTTA[A/T]AAAAAAAAGTTATTT | 10451 |
rs148329618 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107954204 | TGTGAATTTACAAAA[A/G]GAATATTTATAATAG | 10451 |
rs148333110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773798 | TCTCTGTACCACATC[A/T]AAGGATAGGAAGGTC | 10451 |
rs148341091 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107841421 | AGGAGAAACAGTAGC[A/G]GTTGCTATTTTGTTT | 10451 |
rs148355942 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107621081 | ACATGGTCATCATAT[A/C]AAAACTCATTTTTTT | 10451 |
rs148358505 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107904153 | ACTCAGGGCCACTAC[A/G]TAGACACTGGCCAAA | 10451 |
rs148370621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793173 | TCCTCATTTTAGAGA[C/T]GGCTAAACTGAAAAA | 10451 |
rs148391733 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107739650 | TAGAGAAAATAATTT[A/C]TCAACAAAAAACAAT | 10451 |
rs148395256 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107675587 | TACTCCTTTATTGCC[A/G]TGAAGCAGGTAGTGG | 10451 |
rs148429717 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107855106 | ACATTACTGCTGCAC[A/G]CAATCCACTGGCTAA | 10451 |
rs148433258 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107920367 | CACTAATGAAACTTC[A/G]GGGCAAATAGGGACA | 10451 |
rs148443508 | snp | A/G | 0.200182 | 0.244986 | intron-variant | VAV3 | GRCh38.p7 | 1:107736843 | TTTCTTCACAGAATT[A/G]GAAAAAACTACTTTA | 10451 |
rs148446558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107638043 | TGCAGCAAACTAGGA[A/G]TAGAAGGCAATGTCC | 10451 |
rs148451025 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107956396 | AACGTGATTGAGAAT[C/T]CTCAGCAGCTTTTGT | 10451 |
rs148458280 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | VAV3 | GRCh38.p7 | 1:107622687 | CTAAACACTCTCAAT[A/G]TATGCACGATGGTGC | 10451 |
rs148466039 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107811594 | AATTTTTCAAAAGTT[A/G]TAAGATTTAAAATAT | 10451 |
rs148467233 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107905835 | AAGTATTCTATTCTA[C/G]TTAGAAAATGTTAAA | 10451 |
rs148467872 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107843072 | AGTCCACCTTTACTC[C/T]GCCCTTCCCAATAGT | 10451 |
rs148477447 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107845248 | ACAGAAAGGAATAGC[A/G]TCAACATCAACGAAA | 10451 |
rs148479185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107705443 | TATAAACTAGCAGGT[A/G]AGGGTAGGAGGGAGA | 10451 |
rs148494342 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107573852 | TTTATTTATGTCACT[A/G]TCATATTCATTTCAA | 10451 |
rs148498107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802676 | TTGAACTATCATATC[C/T]TAGGATGCATCCCAC | 10451 |
rs148520478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900905 | TTTTTACTCACTCAG[C/T]CTTCAGTTGTTAATG | 10451 |
rs148523507 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107870040 | ATCCACATTGATTGA[C/T]GGGCATTTGGGCTGA | 10451 |
rs148529482 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107789556 | CTCGCTGGTTTGGTA[A/G]CAGTGGTCATTTCAT | 10451 |
rs148539417 | snp | A/T | 0.000248006 | 0.0111329 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107751194 | TCCAAAAAGCAAAAC[A/T]GGTTGGTTCTAAAAT | 10451 |
rs148573995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107935825 | AAAGGGAAAGGTGTT[C/T]CTATTACAATGACAA | 10451 |
rs148576230 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107866326 | TAGACCTGTACAGAT[G/T]CGCCACTGGTAACTC | 10451 |
rs148586101 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107821501 | TTCAAAGAGAAGGGG[C/T]CAGTCATGTGAAGAT | 10451 |
rs148590669 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107744342 | AGTCGAGAAATCTTA[A/G]ATATTCACAGTAGTG | 10451 |
rs148594138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107724362 | CCTTTCTCTGAAGTT[A/G]TATGGCACTTACAAT | 10451 |
rs148597513 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107648459 | TTCTGTTCTGTTATA[A/C]ATGTACATTTTATTG | 10451 |
rs148600119 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107713136 | CATGAATACAGCCAA[C/T]GATAAGGAATAAAAT | 10451 |
rs148604462 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107632487 | AATTTAGTTTTTCTC[A/G]TACTGCCAGTGGTTC | 10451 |
rs148607063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107602604 | AGACAAAAATATATA[C/T]CTATGCCAATACACT | 10451 |
rs148607571 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107915344 | CAGCTTTTAATGCAA[A/C]CCCAAAAACACATGA | 10451 |
rs148643195 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885677 | ACTTACCTGATACAG[G/T]TAAGTACTGTTACAA | 10451 |
rs148644035 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107815390 | CAGAGTTCCAGAGTG[A/G]AGGCTGAAGTACAGG | 10451 |
rs148644871 | snp | A/G | 0.0755793 | 0.179102 | intron-variant | VAV3 | GRCh38.p7 | 1:107798636 | AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG | 10451 |
rs148652291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709681 | TGGTTTCCCCCATCC[C/T]GTTCTCATGATACGG | 10451 |
rs148654278 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107771741 | TATTATCACTGTTCA[C/T]CCCATCAGCTGAGTG | 10451 |
rs148654907 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107680499 | AGCATTTACTATATA[C/T]TGGGCACCTTTGAGA | 10451 |
rs148660539 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594585 | GACATTCTACTGGCT[A/G]TGCTTTTTTTTAAGA | 10451 |
rs148664628 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107582449 | TAAGTTTTAGGGTAC[A/G]TGTGCACAATGTGCA | 10451 |
rs148677089 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107878878 | TGATCATCCTTGCTT[C/T]AATTATTCCATATGA | 10451 |
rs148688311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107666340 | GTTAATGTCTTATTT[C/T]TCAAAAATATAGTTC | 10451 |
rs148706239 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107767520 | CTTCAGCTGATATTG[C/T]GCATGTTATAAATCA | 10451 |
rs148719016 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107659446 | TACGAATCCTATAGA[C/G]TTCAGCTCTTCACAA | 10451 |
rs148740188 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107834443 | CACAGGAAAATAACT[A/G]CAGGAAATTGGAATA | 10451 |
rs148742949 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107731388 | GCTACGTTAATGAAA[G/T]AATCTTCCTAAATTA | 10451 |
rs148750276 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786530 | TAAAGAGGTGACAGA[C/G]AGACAGATATATGCA | 10451 |
rs148756151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613887 | TTTGAGACGGAGTCT[C/T]GCTCTGTCACCCAGA | 10451 |
rs148780779 | in-del | -/ACAGACAG | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107955189 | TGAGGAAGCTAAAGA[-/ACAGACAG]ATAGACAGGTTTAGT | 10451 |
rs148786118 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107891973 | AAAATGTAGATGATT[C/G]TATCTTCCTTACAGG | 10451 |
rs148798511 | snp | A/C/G | 0.00597455 | 0.054357 | intron-variant | VAV3 | GRCh38.p7 | 1:107861662 | TGTCCACCCATATCC[A/C/G]AATATAACCATTCTA | 10451 |
rs148802389 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107781555 | AAATTAAGAAAATTT[G/T]TTACATAAACAAAAG | 10451 |
rs148804020 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693327 | ATCCAACATTCAAAT[G/T]TGTTTCCAAGTTGCA | 10451 |
rs148810601 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107608211 | GGGTGCATTTTAAAA[C/T]TAAGGGTACAAAACC | 10451 |
rs148825605 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107948562 | TTCAACAATAAAGCT[G/T]GCCAGGCGCAGTGGC | 10451 |
rs148826030 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107626263 | TTCAGTTTATGATCT[A/G]TTTAATCAAAGCCAG | 10451 |
rs148829304 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728624 | ATATGTATATGTATA[C/T]GTATATGTATATGTA | 10451 |
rs148830812 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107847916 | TCCTCCTAACTCATT[C/T]TGAGGCCAGTCCTGA | 10451 |
rs148843090 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107836661 | AAGAATAAATAAGAT[G/T]GTTAGACCACTGTCT | 10451 |
rs148845225 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107732625 | CTAGCTCAGCAGTCC[A/G]AGATTGAGCTGCAAG | 10451 |
rs148859459 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107616179 | GCAATATTCACAAAC[A/G]TGGAATCAATCTAAA | 10451 |
rs148868768 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107811652 | ATAACTGGAATTCAT[A/C]AAAAAGCAGAACTAT | 10451 |
rs148881250 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | VAV3 | GRCh38.p7 | 1:107733505 | TGAAAAAAGATTAGA[C/T]GAATGGCTAACTAGA | 10451 |
rs148895892 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107892652 | TCCTCTCTATCTATA[C/T]ATAAAGACTACAATA | 10451 |
rs148897039 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107728839 | ATAGAATTATAATTG[G/T]CACCAAGTATCATTT | 10451 |
rs148899085 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107795416 | AGGGTAGATCTACCT[A/T]ATATTGGCTTCTGTG | 10451 |
rs148926306 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107863115 | TACATTAATTTGAAA[A/C]CCACTGTAAGTTATA | 10451 |
rs148939689 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107741405 | CTCCCTGAAGGGGTG[A/G]TGAGGCAAGGGGTGC | 10451 |
rs148958107 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107858519 | AGCAGTGCGTGAGTG[A/G]GCATTACTGCCTGAG | 10451 |
rs148963523 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689290 | ATCCTCTAAAGAAGC[A/G]TCTGAAAAGATGCCA | 10451 |
rs148973055 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107639971 | TGACCACACCAAATG[C/T]TGGCAAGGATAAGAG | 10451 |
rs148976164 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107923828 | GGACACAAAGCCTAA[C/G]CATATCAAGGCCCAA | 10451 |
rs148983193 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107907696 | ACACGCGCTCTCTCT[C/T]TCTCTCTCATTCTTA | 10451 |
rs148990927 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | VAV3 | GRCh38.p7 | 1:107738097 | ATTCTGAGCAAACTA[C/T]TGCAAGGACAGAACA | 10451 |
rs148994093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107813535 | ATTTTGTTACCACCA[C/T]AGAATGGATAATGAT | 10451 |
rs149002155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707704 | ACTCAAGAGATTACA[C/T]GTATGAAAAACCTTG | 10451 |
rs149006534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107623869 | CAAAATGTCCCTATC[C/T]CTGGCATAGTTCTCT | 10451 |
rs149035796 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587510 | GGATCAGGGCTGTTA[C/T]ATGAAAGCACTATGG | 10451 |
rs149044764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881442 | TGGGGGACATAGTAT[A/G]TGAAAAGGAGGCCAG | 10451 |
rs149045143 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107806022 | ACCACCTATAGCATG[C/G]TACTGAAAAGCCACT | 10451 |
rs149049672 | snp | A/C/T | 4.95154e-05 | 0.00497551 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642728 | GGTGTTCCAGAATAG[A/C/T]TCCTAATGACCTGCA | 10451 |
rs149052499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872080 | CTGACCATCCACAGA[C/G]CAGTGAGACCCAAAA | 10451 |
rs149054391 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107764708 | GTAAACATTTTAAAT[A/C]TACATATACATTATC | 10451 |
rs149058331 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107702476 | CAAGGAGTAAATTGT[A/G]AAGCTAGGATTCAAA | 10451 |
rs149068186 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107657258 | CCACGCCCGGCCTCT[A/G]TATCTTGAATAATTA | 10451 |
rs149082499 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107831232 | TTTATAAACAATACA[C/T]GAAAAAATATGTGGA | 10451 |
rs149102519 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107839147 | ACTGTAGTAGTCAAA[C/T]GCATAAGTTAGCATT | 10451 |
rs149106428 | snp | A/G | 0.000891398 | 0.0210928 | intron-variant | VAV3 | GRCh38.p7 | 1:107760740 | CATTAATATTTTGTT[A/G]AGTGAATAAATGGAC | 10451 |
rs149114755 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107824388 | AGTGAAGGAAACTAT[C/T]AACACATGTGTATAT | 10451 |
rs149116130 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107726469 | GTCTCAGAACCATCT[C/T]TGAGAAAGTCATTGA | 10451 |
rs149120415 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107651108 | TCACCCCATCTACCA[C/T]GTGAGAACACTGAGA | 10451 |
rs149120503 | in-del | -/ATC | 0.239614 | 0.249784 | intron-variant | VAV3 | GRCh38.p7 | 1:107904839 | TAATTACATGTAATT[-/ATC]ATTATATTCAATATT | 10451 |
rs149130595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107605103 | CCTCCAAAATAAAAT[C/T]GCTCATGTTTTTGTT | 10451 |
rs149133045 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964826 | TTGGTGGGCAGCACC[C/T]TGCAATGGATGAGCC | 10451 |
rs149148790 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107715064 | TAGGTTTATGTTTAT[C/T]ACAAAATTAAAGTGT | 10451 |
rs149151469 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107778030 | ATAACTGCCTTAAAT[C/T]TATGTCTAACAAAAT | 10451 |
rs149167681 | snp | A/G | 0.269809 | 0.249214 | intron-variant | VAV3 | GRCh38.p7 | 1:107734959 | cacatagttggaagt[A/G]aaacactcctcagca | 10451 |
rs149172791 | in-del | -/TGTG | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592068 | TACGTGTGTGTGTGT[-/TGTG]GTGTGTGTGTATGTA | 10451 |
rs149179876 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107681949 | ACAGGCGTGAGCCAC[C/T]GCACCCAGCCACGTA | 10451 |
rs149184661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597171 | ATAAACGAAAAATCA[C/T]TTTTAACTTAATTAT | 10451 |
rs149187291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886464 | TGCCACTTATCTAGA[C/T]TTGTGTTCCATTCTA | 10451 |
rs149193256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107953759 | CATAGGGAAGCACGA[C/T]GCTTGTTTATTCAGA | 10451 |
rs149203989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773698 | AGATGGTGATCCATA[C/T]TGGCAGTAACATAAT | 10451 |
rs149217071 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753547 | ATATATATATATATA[C/T]ATACACACACACACT | 10451 |
rs149217354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107668581 | CATACAAAGATGAAT[C/T]TGCAGTCATGGAGTA | 10451 |
rs149234851 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107607693 | GGATAGTTCCCCAGT[G/T]TGCAGTCCCAAATCT | 10451 |
rs149244137 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107891754 | TGAGGCAGGAGAATC[A/G]CTTGAACCCGGGAGG | 10451 |
rs149285007 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107600728 | CTACCAATCCAGGTC[A/G]CTGTGGTATTACTGG | 10451 |
rs149297621 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107887592 | CCAAATTACATCCCT[C/T]ATATTGCCTTTCATA | 10451 |
rs149301102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107854905 | CATAATAATCCCACA[A/G]TGGTGTTCCTGCTTA | 10451 |
rs149305942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107775349 | ACGTTGGGACACCAA[A/G]GCAGGTGGATCATGA | 10451 |
rs149308554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107684830 | GACTCATGTCTGATA[A/G]TATGAAAGAACACTA | 10451 |
rs149339144 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107679020 | AATATAAATTCTTTG[A/C]GGAAAGGGGCCATGT | 10451 |
rs149348367 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963897 | GCACCCAACCTTCCA[A/G]AGGTGTCTGGCTTAA | 10451 |
rs149351954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107912722 | AGGTCAGGGACTAGA[C/T]ACCTGCATCTGCACC | 10451 |
rs149369838 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107801666 | ATCCAGCTGTTCTGT[A/C]TCTCACTTCCAATTG | 10451 |
rs149375831 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107629894 | AGAGTATGTGGAAAA[C/T]ATGACAGTCTACTAC | 10451 |
rs149380675 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107618017 | GAGGAAACTGTTCCA[C/T]CTCAGGCATTAGACT | 10451 |
rs149386337 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107900289 | ATCCATAGTATACTT[C/T]GTAGCCACACGTCAG | 10451 |
rs149420797 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107894358 | AAGGCAGAAATTTAA[A/T]CTGGCATCAACTCAT | 10451 |
rs149423222 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107876882 | CGTATTAGCTAATTA[C/T]TGTATCTTTGCTTTT | 10451 |
rs149433363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757980 | ATTCACACGAGTCCC[A/G]GACTCATCCGTCCAA | 10451 |
rs149436413 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107696635 | TGTAAAGTATGGGTG[A/G]ATTTCAAACCACCTA | 10451 |
rs149440635 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107577187 | CTCAGTATTTCACTT[A/G]ATTGTCACAGCTCTA | 10451 |
rs149446705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107648381 | AAAGGTGTTTATAGG[C/T]TACCAAATATAAAAT | 10451 |
rs149454766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107785970 | CCCCATTAGGATACA[C/T]TACAGCTTAGTGTCA | 10451 |
rs149457422 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107864782 | CAGTGGCACTTATCA[C/T]TGGTTGTAATTATCT | 10451 |
rs149485425 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107753162 | CACATGACTACTACA[A/G]GGATGAACTTTGAAG | 10451 |
rs149500335 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107642081 | GATAGTGTCAGAGGC[A/G]TGTGAACCAGAGCAA | 10451 |
rs149508554 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107926010 | ACAAGGGGCCAGGTG[C/T]GGTGGCTGCCTGTAA | 10451 |
rs149509153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860469 | CTTTAAGCTAGTTCA[C/T]GAACTCATTTCTGTA | 10451 |
rs149517437 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107739213 | AGAAAAATGAGAGAG[C/T]TTGATCCTCACTAGG | 10451 |
rs149518910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107815270 | ACCTTGACTCAAGAC[C/T]TGCTTTCTGTCAATC | 10451 |
rs149523730 | snp | A/C/G | 0.00086931 | 0.0208308 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107766532 | CTTGCATTAGGTTCC[A/C/G]ATGAAGTTTTACAAG | 10451 |
rs149535735 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593966 | GCTAAGTGCTTTATA[C/T]AGAACACCTCATTTA | 10451 |
rs149561832 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107917946 | GAATTAAGGACTGAG[A/G]TGCACAGACCCAGGA | 10451 |
rs149565281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107882444 | AGACGACCATGAAAC[C/T]GATTTACAAACATTA | 10451 |
rs149570483 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107809554 | GTCATAAATATTTTT[A/G]AGAAAACTAAAATTT | 10451 |
rs149579348 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107874280 | ATTATACATGTGTTT[A/G]GTGTGCATACGGATA | 10451 |
rs149583098 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107674024 | CTTGGACAACAAATA[G/T]CTATTGTATTTCTGT | 10451 |
rs149583784 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107703957 | GCATAACTGCCAGCC[A/G]TCTTAGAAACTAGCT | 10451 |
rs149585367 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590265 | ATTCCCATGCTTTTC[C/T]AGTTTCAACTTAGCA | 10451 |
rs149593145 | snp | C/T | 0.00755907 | 0.0610114 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572276 | TGACCCTCTTTCTGT[C/T]CCAGAAATGAATAAA | 10451 |
rs149596534 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107946042 | GCAGCAGGGTCCATA[A/C]TCCAAGCATGGGGAA | 10451 |
rs149631041 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | VAV3 | GRCh38.p7 | 1:107761254 | CAAAATTAGCCGGTC[A/G]TGGTGGCAGGTGCCT | 10451 |
rs149633627 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841358 | AATAAGAAATATGGG[G/T]AAAAAAACTAAAGCA | 10451 |
rs149640497 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107728282 | CACAAGATCTGTTCT[A/G]AATGAAGAGGAATCA | 10451 |
rs149646554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654213 | TATTTCAGATTTCAA[C/T]ACTTAATGAATGCAT | 10451 |
rs149648671 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107620922 | GGTAGAGGAAGAGAC[C/T]GTGGTTGTATAAGAA | 10451 |
rs149649164 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107940291 | ACCAAAGAATTATAA[A/G]GTCAGGCAAGACTAT | 10451 |
rs149666818 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107883272 | AGCACCCGGCTCACA[A/T]CTGTTATGGTAATAA | 10451 |
rs149675460 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107780655 | CAAGTAGCTGGGATT[A/G]CAGGCACACACCACC | 10451 |
rs149680798 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107768834 | GGAGATGTATATGAA[G/T]ACTTACACAGTAATA | 10451 |
rs149687299 | snp | A/G | 0.0217236 | 0.101931 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591431 | AATGAATGAATGAAT[A/G]AATAAATGAATGAAT | 10451 |
rs149688251 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107675347 | ACTAGGAGATGGCTG[C/T]TACTATTACTTCCAT | 10451 |
rs149693654 | in-del | -/AA | 0.0733688 | 0.176922 | intron-variant | VAV3 | GRCh38.p7 | 1:107830226 | TTTTTTTTTTGAGAC[-/AA]AAGTCTTGCTCTATC | 10451 |
rs149717424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732493 | CTATACCAGGAAAAT[C/T]GGGACACTCCCGCCT | 10451 |
rs149724882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107955861 | GAACCACTAAAGTTA[C/T]AAGGAGGTTGTCTGA | 10451 |
rs149734524 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107842741 | TTAATTTTTCTTCTT[A/G]TTCTCTATCATATGT | 10451 |
rs149742042 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107671765 | AGTTAGGCTTAGTTT[C/G]TCATATTTTACCAAA | 10451 |
rs149751309 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107622568 | CTTAATGCACTCCTG[C/G]AATAGCACTGAACAA | 10451 |
rs149758509 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107943485 | ATAGCACTCTTAAAA[C/T]TTCCCAGCACTTTGG | 10451 |
rs149761641 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107892525 | TTTTTCTAATTCTCC[A/T]TCCCCTTTTTTCTAT | 10451 |
rs149769032 | in-del | -/C | | | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689791 | TCAGAAGAAAGATCG[-/C]CCAAGAGCGCTGGTT | 10451 |
rs149769439 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107728636 | ATATGTATATGTATA[C/T]GTATATGTATATGTA | 10451 |
rs149782590 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107610881 | CTATTAATGGGATTT[C/T]TATATTTGGTGATTG | 10451 |
rs149822952 | snp | C/G/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107789255 | GCTGTCAAAGTCACA[C/G/T]AACTCACTGGCAAAG | 10451 |
rs149831315 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107857810 | GGGCCTCTTAAAGGT[G/T]GAATGAAGAATGCTT | 10451 |
rs149836746 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688761 | CAACCTTTCTTTCAA[C/T]ATGCCTCGTTTTAAG | 10451 |
rs149883785 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107914870 | GAACAAAACCAGCAC[A/G]CATAAAGCAGCAGCA | 10451 |
rs149886497 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107743157 | CCAGTCAGGGCCTTC[C/T]TCCATCCTAGCGAAA | 10451 |
rs149890807 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107681136 | TGAAGTAGTTACACC[C/T]GGCCTCCTAAACTCT | 10451 |
rs149893423 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107805133 | TTTATTATGCTTCTT[G/T]GTAAAGCCTTATTGG | 10451 |
rs149897137 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107853838 | ACTCCTTTATAAGAG[C/G]TAACTAAAGAATATT | 10451 |
rs149897857 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | VAV3 | GRCh38.p7 | 1:107735533 | AGGGGATATCACCAC[C/T]GATCCCACAGAAATA | 10451 |
rs149900983 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107632181 | ATAGTGTCAAAATTA[C/T]CATGGTCTCTTACCA | 10451 |
rs149907026 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107702062 | TTACTGTATTAGTCC[A/G]TCCTCCCACTGCTAT | 10451 |
rs149937632 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107910249 | AGCTTTTCCATACAC[A/G]GATAAGAACATAAAA | 10451 |
rs149945238 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107798482 | CTAGCACTTTGGGAG[C/G]CTGAGGTGGGCGGAT | 10451 |
rs149960403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107698160 | TAAATGAGTTAACAA[C/T]GGTAAAGTACAAATG | 10451 |
rs149961443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107581205 | GGATGCTTCGTTTAA[C/T]GGCATAACTTTCCCC | 10451 |
rs149966916 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107878287 | ATACCATTATATCTA[A/C]GAAAATTAACAATAA | 10451 |
rs149972221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107936862 | ATACACCTGTGTCAC[A/G]CTGCTCCTTCCCCGA | 10451 |
rs149979381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107868029 | GAGAAGGGCTGAAAA[C/T]ACAAGGGCATTGCTA | 10451 |
rs149981127 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107759943 | AATTTGACTAAGTTG[C/T]TTTGAGTTTAGGTCT | 10451 |
rs149996441 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649905 | AAACACAAAAGCAAG[A/T]GAATCAATGTAATAA | 10451 |
rs150025561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107928652 | CTTTATCAGAATTGT[C/T]TAAGCAGAATTAGTG | 10451 |
rs150032689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107754314 | GATGAGAGGCTACTG[A/T]GACTGGAAAACTGGC | 10451 |
rs150040971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107816568 | TAATATATTTCACTC[C/T]AATGCTAAATAGGCC | 10451 |
rs150041613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886394 | TTCCCCTCCATGCTA[C/T]GCAGCCTCTCGGGGA | 10451 |
rs150042719 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107721251 | GAGCATATGTCCATT[C/T]AGCAGAATAATTAAA | 10451 |
rs150046098 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107644792 | CTCCATAAGAGGCTG[C/T]AAGGTGTTAGGGATG | 10451 |
rs150050808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107773563 | TAACTAACATAAAGA[C/T]AGATGAGGAGAGGAA | 10451 |
rs150055565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107596978 | CTAATGTAATAACCA[C/T]ATGCCATCCTTCAGA | 10451 |
rs150080794 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939247 | AAACTAAATCTCCTT[C/G]CAAGTCCAAAAATGT | 10451 |
rs150085302 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107700366 | TACATAGGTAAACGC[A/G]TGCCATGGTGGTTTG | 10451 |
rs150095042 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107653473 | TCAGTCATTGTAAAC[G/T]TCTATGAGTCCACTT | 10451 |
rs150116705 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107662582 | AAAGCACTAAGAGTT[C/G]AATGGATTTTATTCA | 10451 |
rs150122036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107876277 | TCACGGGTACCTTGA[C/T]AAAAGCAGGCTCTAT | 10451 |
rs150127668 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107933883 | AAGCATGCTATCTGT[A/G]GGTAAAGCAATGTTT | 10451 |
rs150139754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757593 | TTACACTGACATTGA[C/T]CCCTATTGTTATGAA | 10451 |
rs150141660 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107819795 | TGATAACAGTTGTTA[C/T]AAATAACAACTGCTT | 10451 |
rs150143988 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107887286 | TAATGGCTTCAATCA[C/T]GGATTGAATTTAGTA | 10451 |
rs150148423 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107646801 | ACTCTACTAATAGTC[A/G]TGTGTTTCTGGTTAA | 10451 |
rs150153678 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107615667 | TAAACAGGCAACATA[A/G]AGAATGGGAGACAAT | 10451 |
rs150158192 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107599505 | AAGGAAACAGGCAAT[A/G]GAGATGGTTTATAAA | 10451 |
rs150171960 | in-del | -/AT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107850861 | TAAAGGCTACCACAC[-/AT]ATATATATATATATT | 10451 |
rs150197293 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107783507 | GCTGTTAAGGCTCTG[A/G]AGGTGGACAGCCCCA | 10451 |
rs150197358 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107885159 | ACAAGAATCGCCATG[C/T]TTGCCTTGCCCCAGA | 10451 |
rs150197799 | in-del | -/ACAGA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107644959 | TGTATACTCGAGTAT[-/ACAGA]GTATACACTAGTATA | 10451 |
rs150210790 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592965 | CTTTCATGGAGTCAC[C/T]GAAGTTTCTAGAGGA | 10451 |
rs150212689 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107678124 | AGCTTGAAAAAAAGT[C/T]GGCTATTTTAAAAAC | 10451 |
rs150214852 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963371 | CTGAAGGGGTACCGA[A/G]AGGTAGCAATCACCA | 10451 |
rs150229596 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107770180 | CGGGAATGATCTTCA[C/T]TGGCATATGTACACG | 10451 |
rs150231643 | snp | A/G | 0.046775 | 0.145601 | intron-variant | VAV3 | GRCh38.p7 | 1:107849725 | CAAAATTGACACATG[A/G]GATCTAATTAAAGAT | 10451 |
rs150258442 | snp | A/G | 0.181022 | 0.240296 | intron-variant | VAV3 | GRCh38.p7 | 1:107737754 | ACTTTTACACTGTTG[A/G]TGGGACTGTAAACTA | 10451 |
rs150267527 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107958709 | GGTATACATGTGCCA[C/T]GGTGGTTTCCTGCAC | 10451 |
rs150271681 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107623747 | ACAAAAGAACAAAAC[A/C]ATAAGCTATGCATTT | 10451 |
rs150282528 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107844256 | AGGGAAGCCTTGAGG[A/G]ACTGTGCCACGAGGG | 10451 |
rs150283564 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107907605 | GTGGATTCATTACCA[C/T]GACAGTAGTTGTCAT | 10451 |
rs150292630 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107795860 | TGATGAGGCCAGGTC[A/T]AAAGTGCTGAGCTTA | 10451 |
rs150296857 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107730326 | CATATTTATTTAACG[A/T]TCATCTGAATCCACC | 10451 |
rs150305610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695891 | TAAAAGATTATCTAC[C/T]TCTCATTGAGCCCCT | 10451 |
rs150329690 | in-del | -/AAGTA | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107712738 | ATGATGAACAAAAAT[-/AAGTA]AAGTCCCTGACTAAT | 10451 |
rs150330514 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107902745 | AAGAGAGGGGAAGGA[C/G]AGCGAAGGCCAGTAG | 10451 |
rs150337981 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107891605 | GCACTTTGGGAGGCC[A/G]AAGCGGGTGGATCAC | 10451 |
rs150344617 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107790938 | TGATCTGCCCGCCTC[A/G]GACTCCCAAACTGCT | 10451 |
rs150346769 | snp | A/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107871691 | CATCTCACAAAATAC[A/T]AATTATCATTTGTGT | 10451 |
rs150351426 | in-del | -/AAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107687682 | GGGGAACTCTATATA[-/AAC]AACATCAAACAACAC | 10451 |
rs150352004 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107860034 | CAAATGTCATGATGC[C/T]TATCTATATTTACTT | 10451 |
rs150354551 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107752985 | AGGCACTTGAATAGA[C/T]ATTGGTACACCTGTG | 10451 |
rs150406526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746542 | CCCTATATGTATAAA[C/T]CTGTAAGGCGGTGGC | 10451 |
rs150408296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107824081 | AAGAAGCAGGGAGAC[A/G]TGAACTGAGTAGAAA | 10451 |
rs150416566 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | VAV3 | GRCh38.p7 | 1:107714880 | GTATTTTCTTATCTA[C/T]TATATATTACACTTC | 10451 |
rs150425650 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917431 | AACAAGTTAGGTAAC[A/T]GCCAGAATTCTAGCC | 10451 |
rs150429946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589940 | GCTACTTTATGTTCT[A/C]CTGAGTTAAATAAAT | 10451 |
rs150440728 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107808220 | ATGGGCTAAGAAATG[C/T]TAATGCTTAGAAACT | 10451 |
rs150460103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911696 | CACTATTATCTGCCA[A/G]GGGAGAATTAACTGT | 10451 |
rs150474715 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710364 | AGCAAATGTCAGTGC[C/T]TCAAAAACACCTGTC | 10451 |
rs150482374 | snp | A/G | 0.000131981 | 0.00812237 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107772735 | AAGTAAAAGTCCTAC[A/G]GGCTGATGTGCTTCC | 10451 |
rs150493658 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107800736 | ATCTCTTGTTATATG[G/T]ATAGTTTGCAAATAT | 10451 |
rs150499314 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107744213 | CCCACTACCATTAGT[-/C]CCTTGTGTTTAAAAG | 10451 |
rs150501376 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107868718 | GATGTAGAGGCTTAA[C/T]AAATGGTCTCCAAAT | 10451 |
rs150504178 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857023 | CACTGTGGATGACAT[G/T]GTGTGATGGTTAATA | 10451 |
rs150511568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107826582 | ACTGCTCTAGTGTAC[C/T]GCAGTTCACTGGCAG | 10451 |
rs150524507 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107638493 | AGATGTATATGACCT[C/T]AACTCTGAAAACTGC | 10451 |
rs150525977 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107716439 | TTGAGAGTTTTTAGC[A/G]TGAAGCGCTGTTCAA | 10451 |
rs150529687 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920514 | CAATATGAAATGATG[A/G]TATCTCACAAATGTG | 10451 |
rs150543167 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812081 | ATTTTCTTAGAAAAT[G/T]TAGGCTTAAAAAAGA | 10451 |
rs150546237 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107883245 | AAAACACATGCACCC[G/T]CTTTGCTCTGCAGCA | 10451 |
rs150560066 | snp | A/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591205 | AAAAAGCCCTTCTCT[A/G]ACCCTGAAGGCTAAA | 10451 |
rs150578527 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107712306 | GGCCCAACACAAATC[C/T]GTAAACTTTCTTGAA | 10451 |
rs150590758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107586663 | GATGAGGAATTGATT[A/G]ATTATTTTGAAAAAG | 10451 |
rs150599936 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107880978 | TAATTTTTTTTTAAA[C/T]ACATACTGAGGCTTA | 10451 |
rs150600162 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107775068 | TACATTCGGACCTTC[A/G]GCCACCAGGTAGAAA | 10451 |
rs150606504 | in-del | -/A | 0.243633 | 0.249919 | intron-variant | VAV3 | GRCh38.p7 | 1:107909449 | ATGAGTAGACAATGG[-/A]AAAAAAAATGGTCAC | 10451 |
rs150607357 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107842240 | TAGTTCCCAAATTCT[A/G]AAATGAGTCCACTAC | 10451 |
rs150611337 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107762252 | GTGCTTAAGAAAATA[C/T]ACTGTTGCTCACAAG | 10451 |
rs150614326 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107671094 | AGGCCTATAATGGTA[A/G]GTGGAGGTAGAGAAA | 10451 |
rs150643545 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107950277 | AGGCAAAAATGTGCA[C/T]ATAAATGTAACTTGT | 10451 |
rs150657856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936150 | CAAAAATATGAATTG[A/G]TAGATAAAACATCCT | 10451 |
rs150671964 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107725145 | GGAGAGGGGCATGTC[A/G]GTTTAGAGAGGTCAC | 10451 |
rs150690358 | in-del | -/TCAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107695723 | GCTAAACCAGGAAAG[-/TCAA]TCAGATTTCCAGAAG | 10451 |
rs150706014 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107894145 | ATAGTTGACTGTAAA[C/T]GGACACTGTTTACTC | 10451 |
rs150709452 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832729 | TCCAAAGTGTTGATG[C/G]TTCAATATTCATATT | 10451 |
rs150719548 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107785174 | CTAGCACATTAGTGC[C/T]GTTGATGTTATTTGT | 10451 |
rs150726279 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107612338 | TTGAGAAATTTCTAA[A/G]AGGATAGTAATTTTC | 10451 |
rs150732558 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107680823 | AGGAGGCAAACTGCC[A/G]AAGTTCAAACAGCAA | 10451 |
rs150744832 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965933 | GAGCAAAGCGCGTTA[A/G]CCCTGGGCAGCTCCT | 10451 |
rs150787299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738912 | ACAGTAGCACAGTAA[C/T]CACCACTGTCAGGTT | 10451 |
rs150791928 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107960498 | AAAAGAAAGGTAAAT[C/T]AGGCCATGTCACTCC | 10451 |
rs150801130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107909915 | TTCACATTCCAAATC[A/G]GTTACAGGTTATTTG | 10451 |
rs150805562 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107846188 | CCAGAATTTCATATC[C/T]AGCCAAACTAAGCTT | 10451 |
rs150815828 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797525 | AGGGCTCCAAAAAGC[A/C/T]TAAGAGTCAAGTCCA | 10451 |
rs150820260 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107731702 | TTTCAGAGGCAGTCC[A/G]TCCCTCATCACAAGA | 10451 |
rs150842219 | in-del | -/CCAGGGG | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107753293 | GTAGATTGGTAGTTT[-/CCAGGGG]CCAGGGAAAGAGAAG | 10451 |
rs150856088 | in-del | -/T | 0.0372196 | 0.131242 | intron-variant | VAV3 | GRCh38.p7 | 1:107856818 | AGGCTGGAGGATCAC[-/T]CTTGAGCACAGGAGT | 10451 |
rs150861820 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107904327 | TGATGTCCAGCAGGC[A/G]GGTACCAAACATGAA | 10451 |
rs150865350 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107873477 | TCAAGGAAGATTTTT[G/T]TAAAGGTGCAGGAGG | 10451 |
rs150868119 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107793683 | GTTTTAAACACCAGG[C/T]TAAGGGGTCTAGATT | 10451 |
rs150870743 | snp | C/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107704573 | TTAACTCTGCCACAA[C/T]TGTCTACTCTTCCCA | 10451 |
rs150875911 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107621389 | GCTATCCTACAACAT[C/T]TGGAGAATTCAAAAC | 10451 |
rs150877825 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107703537 | GCCTAGCACAGAGAA[C/T]GGCACAGAGGGTCCT | 10451 |
rs150881859 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107693452 | CAAATGAGGTGCTTC[A/C]TTCAGAAATGCACTG | 10451 |
rs150886240 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571569 | CAAAGTTCGGCTGAC[A/G]GCAACAGACAAAACA | 10451 |
rs150892112 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107644493 | AGTCAAGAAAGAAGA[A/T]CTTTTAAACCTCAAA | 10451 |
rs150902760 | in-del | -/A | 0.356597 | 0.226135 | intron-variant | VAV3 | GRCh38.p7 | 1:107880814 | AAAAAAAAAGAAAAG[-/A]AAAAAAAGCACCAAA | 10451 |
rs150918236 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107800241 | AGGTTATATAATAAT[C/T]CAATATTTAATTTTT | 10451 |
rs150925864 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107627250 | TCCATCACTCTCTGT[A/G]AGGTATCCTGGGTCT | 10451 |
rs150928075 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107709998 | AATAAGTATGACAGT[A/G]TAGTTAGTAATACAA | 10451 |
rs150950265 | in-del | -/TAAC | 0.0667028 | 0.170006 | intron-variant | VAV3 | GRCh38.p7 | 1:107799439 | GTAAGAATGGTAACT[-/TAAC]TAAATATGAACCAAG | 10451 |
rs150972869 | snp | C/T | 5.58935e-05 | 0.00528617 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107705054 | CATAGTCTGGTCTTA[C/T]GTTAGACCTAAAAAA | 10451 |
rs150975526 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107876184 | AGTGAAAAACTATAT[C/T]AGATGCTGCAGACGG | 10451 |
rs150976530 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107795465 | AATTGTAATACAATG[C/T]TTCTGTTTTGGTACT | 10451 |
rs150985081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694922 | AACATATGATGTCAG[A/G]GGAGCACAGAGGACT | 10451 |
rs150986952 | snp | A/G | 1.65701e-05 | 0.00287833 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107757301 | AGATTTGCCTTCTCA[A/G]TCGGATCAGTGGTAT | 10451 |
rs150989773 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107662409 | GGATTTCTATAAGGG[A/G]AAAAAAAATATCTGC | 10451 |
rs150992825 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107574449 | AGAACCTCAATCAAA[A/G]TAAGGACTAGTTTTT | 10451 |
rs151000356 | in-del | -/GA | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107769489 | CTAACCTCTAAATGT[-/GA]GAGTCTGGAGAGCTG | 10451 |
rs151006054 | in-del | -/GCAAAGGCCTGGGGCTTGCACCCTCTGAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701279 | CACCACATGGAAGCT[lengthTooLong]GCAAAGGCCTGGGGC | 10451 |
rs151028853 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | VAV3 | GRCh38.p7 | 1:107870393 | TGATCATTAGTGATA[C/T]TGAACATTTTTTCAT | 10451 |
rs151037707 | in-del | -/A | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107655731 | ATTAATAACTAGAAT[-/A]ACAGAAGGTGCTCAA | 10451 |
rs151038863 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107751582 | GATACAGACACTGCC[C/G]TCATGAAGCACACTG | 10451 |
rs151040052 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107656020 | TGCTAATTAGTACAG[A/C]CCCTATGGAAAATAG | 10451 |
rs151050246 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107610618 | AGGCATGGAAAATAC[C/T]TATTTTTCCATTTGT | 10451 |
rs151052194 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107640043 | GGTATAGGCACTTTG[A/G]GTAACAATTTAATAA | 10451 |
rs151060727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107829244 | CTTACTACAGCACTA[C/T]TGTATTTTAAATCTG | 10451 |
rs151060826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107924056 | AAAACAGTACTGTTT[C/T]GGACTTTTCACTCTG | 10451 |
rs151064340 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107884957 | GTTTAGCAATAGTAA[C/T]GTCAGCAGTAAAAAT | 10451 |
rs151104546 | snp | C/T | 0.000164853 | 0.00907741 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107603066 | TGCTAATTGCATATT[C/T]TCCTGACTCTTTGGT | 10451 |
rs151110422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107888607 | GGGATGACAGGTGCC[C/T]GCCAACACGCCTGGC | 10451 |
rs151118376 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107881631 | CATGAATAGCTCGCT[C/T]ATTTCAAGGTGAGGA | 10451 |
rs151122345 | snp | A/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874987 | CACAACAGGCCGTGA[A/G]AAATGTCCTTATGTT | 10451 |
rs151123085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107958465 | AAATCTCACAGACAA[C/T]AGTGATGAATTATTT | 10451 |
rs151123864 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107776927 | ACTCCAGCAGCAGAT[A/T]CTATTTCTTTTAAAT | 10451 |
rs151127766 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107713672 | TACACTGAAGGGTTT[C/T]CATAAAAGGGAAATT | 10451 |
rs151131413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107843984 | TAACTTTAACTAACC[C/T]ATAAGAGACTTTAAC | 10451 |
rs151137098 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107673054 | ATTGTTAAATAATAA[C/T]CAGCCATATGGAAAA | 10451 |
rs151142715 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588159 | CTGGTAAAGATCCTG[A/G]AGTAACTAAATAAAA | 10451 |
rs151170119 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107951772 | AAACCATAATGAGAT[A/G]CTATCTCATATCAGT | 10451 |
rs151176426 | in-del | -/CACATCCAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857022 | CACTGTGGATGACAT[-/CACATCCAC]TGGTGTGATGGTTAA | 10451 |
rs151182457 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772613 | TAACAAGTCATAATT[A/G]TATAGTTATAAGCAA | 10451 |
rs151183247 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107839792 | AGCTAAGCAAACCAA[A/G]AAAAAAGAAAGATGA | 10451 |
rs151185880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902221 | GAGGCTAGACCAAGG[A/G]TCTCTACAGACTTTG | 10451 |
rs151190550 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667277 | CAGAAATTCTGGAAG[A/G]TGGATGCTAATAACA | 10451 |
rs151192116 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107735454 | ACAAAATAGATAGAC[C/T]GCTAGCAAGACTAAT | 10451 |
rs151198003 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107726964 | CTCACACAATGAGTA[A/G]TAATCATCTAACATT | 10451 |
rs151199833 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107619290 | TTTACAGAAACTAGT[A/G]AAACAACAAGGCAGA | 10451 |
rs151239461 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896624 | ATCGCAACCCAAGCC[A/T]CATGTACTAAGATCA | 10451 |
rs151254230 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107697863 | GTTCTGCCTAAAAAA[A/C]CATTAGAAAATCACT | 10451 |
rs151256396 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107613991 | TGGTATGAATTCCAG[A/C]CCTTCATCTGGATGG | 10451 |
rs151273089 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107886658 | TTCCTCTTCTTATGA[A/C]TCTTATTCATCTAGG | 10451 |
rs151273230 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | VAV3 | GRCh38.p7 | 1:107867689 | GGGACAAAGCAAACG[A/C/T]GGCCTTGGTGAGTGG | 10451 |
rs151284252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107682004 | AGCACTTCTCTTGTA[A/G]GTTTATTCTTCATGA | 10451 |
rs151286782 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107746291 | ATATATAATATAACC[C/G]TTATTTATAGAAGCC | 10451 |
rs151294114 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107633550 | AAAATGTTTTCTGTC[C/T]GTGGCACACTGTTAT | 10451 |
rs151323123 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962510 | TAAGCATGTTAAATA[C/T]GTCAAGTTGTTTCAT | 10451 |
rs151329533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107848040 | GCAAACCAGCCAGGT[A/G]TGGTGTCTCACGTCT | 10451 |
rs151334139 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107816071 | TCAGGCAGTAATGCT[C/T]GCTCATCCACCCCTC | 10451 |
rs151337534 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107740009 | CAATGCTTCTTGGCT[A/G]GGCATGGTGGCTCAC | 10451 |
rs180671251 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107934674 | CAAAAGTCTCGAAAA[C/G]GAAACTCTTAGTTCC | 10451 |
rs180676265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964244 | CCTCTTTTAGGAAAA[C/T]ATGAGTACAAGACGC | 10451 |
rs180682076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107954970 | ACAGTGCCTGCCTCA[C/T]GGTGTTGGACAATTA | 10451 |
rs180685270 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107913773 | AAAAATTTTAATTTA[A/C]AACTTCACAAATTAT | 10451 |
rs180708733 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | VAV3 | GRCh38.p7 | 1:107922946 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 10451 |
rs180713146 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107943673 | CTTGAACCTGGGAGG[A/C]AGAGGTTGCAGTGAG | 10451 |
rs180720986 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107905576 | GAATGAAACTTTACA[C/T]TGCTGCCCAGATTGC | 10451 |
rs180728886 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107847352 | CCACCCTAATATCAC[A/G]GTTAAAAGAACTAGA | 10451 |
rs180729762 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107613812 | CCAATCCAGACAGCA[C/T]TTGAATTTTCATTGG | 10451 |
rs180729824 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107864382 | ATCCAAGCACTTTGG[G/T]AGGCTGAGGTGGGTG | 10451 |
rs180730500 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107830661 | GTCACACCCTTCCAA[C/T]ATATCTTTGCTCATT | 10451 |
rs180735613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888108 | AATGGTTACTTTATA[A/G]TCTTGTATTATTATT | 10451 |
rs180737574 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812397 | GTGTGCCCGTTTTCA[A/T]TACCTAAAAAACTCT | 10451 |
rs180747250 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107792401 | CAGCCTCAAACACAC[A/G]GGCTCAAGTGATCCT | 10451 |
rs180748671 | snp | C/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591521 | TCTGTTCAGTACATG[C/G]TAGTGTTCCACACGT | 10451 |
rs180752533 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107669724 | CCCTTTCATCTATTC[A/G]TGAGGTGCTGTATTA | 10451 |
rs180754479 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658552 | ATGGTTGAACTAGTT[A/T]ACAGTCCCACCAACA | 10451 |
rs180759341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635798 | TCATAAATAACATGA[C/T]TGTAAAAGAAGTGCT | 10451 |
rs180760475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649050 | AAAACAGCCTCAAAA[A/G]CCCTCAAAAAACAAA | 10451 |
rs180765190 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688816 | AGGTACTGCATTGAC[A/G]ATTTGTAACAATAGC | 10451 |
rs180766543 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107677218 | TTCTACATAGAACTG[C/T]AGTATAAATAAGATC | 10451 |
rs180777733 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722448 | CTAAGACAAAAATTG[A/G]AACAGCCTTGCTGAC | 10451 |
rs180781773 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107708214 | AAAAAAAAAAGTTCT[A/G]CTGCTACTACATAGA | 10451 |
rs180783348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761197 | GATCAAGACCATCCT[A/G]GCTAACATGGTGAAA | 10451 |
rs180790283 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107779325 | CAGGCACTCTTCATG[A/G]ATGAGACATAGTACC | 10451 |
rs180791558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107715226 | CTGTTCCACCGAGCA[C/G]TCAAATTTGTTCTGA | 10451 |
rs180797810 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107742924 | GTCAGGAGAGATCTC[C/T]CTCACAAAGTAACAT | 10451 |
rs180798470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736165 | TTCAACAGTCCTTCA[C/T]ACTGAAAACTCTCAA | 10451 |
rs180801722 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107754224 | TGAAGACAACAACAA[A/C]AAAATCTTGACAAAT | 10451 |
rs180807207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107801532 | AAAACCTAACTTAGA[A/G]GTATGCACCTGTAAC | 10451 |
rs180809235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699172 | AAGGCAAGTCCCTTC[C/T]AACTATGAGCCAGTA | 10451 |
rs180815937 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107728375 | CTTTGGGCAAATTAC[A/T]CTGTAGAGGAAGTCT | 10451 |
rs180824824 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771098 | AAGGTATTTGGCAAA[G/T]TAAGTAAAGACCTTC | 10451 |
rs180866364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107789514 | CCAGACTAGGAGAAT[A/G]AAATGACAGTCCTTA | 10451 |
rs180931264 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107946629 | CAGTCATGCTATCCA[C/T]AAAAGAGAAGGACTG | 10451 |
rs180939534 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107908242 | TCCCCCAGCAGTGGC[C/T]GGTAGAAGTGGGGAT | 10451 |
rs180945433 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107928568 | ACAAAGGGATTGAAA[C/T]AATTTTCAAAGGTTA | 10451 |
rs180946647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891301 | CATTCTCTCCTCTCA[C/G]ATGTTATATCATTTT | 10451 |
rs180952738 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107938954 | TCAAACTGTGTTCAA[A/G]TAAGGCAAACGCTGA | 10451 |
rs180954880 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107903021 | TCTGCTAGTGTGAAA[C/G]AAATAATTTTAAGGA | 10451 |
rs180963836 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107958241 | TCTTTTTGGGAAATA[A/T]CAGTTCTTCCTCCTT | 10451 |
rs180973094 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107574439 | ATTCTTCATAAGAAC[C/T]TCAATCAAAGTAAGG | 10451 |
rs180982323 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920333 | TCATTACCACACACA[C/G]GGTATAAATACGGCC | 10451 |
rs180987917 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107861654 | GTGTCCAGTGTCCAC[C/G]CATATCCGAATATAA | 10451 |
rs180995673 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107654965 | TAAAATAATAACAAA[C/T]TGTGCCAAGAAGTTA | 10451 |
rs181004633 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107694192 | GAAATAATTAGAGAA[A/C]AATTTAATTCAGGCT | 10451 |
rs181006742 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881883 | TTAAAAAAGGAAACA[C/T]TTGAAGGTCAAACTG | 10451 |
rs181007952 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673665 | ACTTAACACCAAGTC[A/C]GTATACTTGTCAAAG | 10451 |
rs181017583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711055 | GTTCTGGAAGATCTA[A/C]TCACTGTAATATGAC | 10451 |
rs181020847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107725639 | CATCCCTCAGCCTCC[C/T]GAGTAGCTGGGATCA | 10451 |
rs181021706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586677 | TAATTATTTTGAAAA[A/G]GAAAAGGAAGGAATG | 10451 |
rs181022443 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107738534 | TTCCTTGCCATCTCC[C/T]CAACTAGCCTGCTAT | 10451 |
rs181025645 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107834566 | GAATAGTCATCATGA[C/T]AGACCACATTCCAGG | 10451 |
rs181036411 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107796363 | CAGTGAGCAAACAGC[A/G]AACCAGTCTCATTGG | 10451 |
rs181038586 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107608187 | CAGTAGGATTTTACA[C/T]ATTGGCAAGGGTGCA | 10451 |
rs181043956 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107816332 | GATAAAATAACCATG[C/T]CAATTCCACAAAGTG | 10451 |
rs181070393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107704733 | AGAAGAAGAAAAAAA[A/G]TATCAACAGTGCTCT | 10451 |
rs181089936 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107718774 | AACAAAAAGAACAAA[G/T]CTGGAGGCATCACGC | 10451 |
rs181106203 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774359 | GGCATGAGCCACCGC[A/G]CCTGGCTGACTTTTC | 10451 |
rs181107793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750495 | TGCATCACTTTTAAC[A/G]TCTATTTCTCCCAGA | 10451 |
rs181111284 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107733540 | ACAGTGTAGAGAAGA[C/T]CTTAAATGACCTGAT | 10451 |
rs181120201 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107784405 | TTGTCAATGAGCTTT[C/T]TCAACATTTTTCTGC | 10451 |
rs181124044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767317 | ATATGAGGCAACTTG[A/G]ACTAGGTGCCAATTC | 10451 |
rs181151793 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965673 | CCCCTAGTGGTGTTT[C/T]GGCACCCTCAAAGTG | 10451 |
rs181159165 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107923247 | TGGAATTGCTTAACC[C/T]CCAACTAATAATGAG | 10451 |
rs181168235 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107888431 | AATGCCTTTCAGCAG[G/T]CTTCTTCTCTACCCT | 10451 |
rs181174629 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107905898 | AATTCAAAGTCAAGC[A/T]GGACTGCCCATGTAA | 10451 |
rs181177614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107865240 | AAGGTCCAATTTCTG[C/T]GGGGCAGAGAAGCAG | 10451 |
rs181189021 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107580621 | GTAGCGTGACTTATT[A/G]TTGCCACTCTTCCTA | 10451 |
rs181199587 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831722 | GCTTATGTTTTAAAC[C/G]TCTATTTTTGGGATA | 10451 |
rs181201166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107623360 | ATTGTTTCTTGATTA[C/T]TGTCAATCACTTACT | 10451 |
rs181213732 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107648417 | TAAAATTTCATGTGT[A/T]ACTTGAAAATCCATG | 10451 |
rs181215622 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107601034 | GTCTTGCAGAGATGT[A/G]GAGAGCCCCTGTGCG | 10451 |
rs181234458 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107952985 | TTTCATTTTAAATAG[A/C]ACAACTTTCAGTTCA | 10451 |
rs181256204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613248 | TTTAATATATGCTTC[C/T]TGACTCTGAAGATTA | 10451 |
rs181259315 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107912041 | AAAGTAAATACCAAG[C/T]GTTTTTTGTTTGTTT | 10451 |
rs181270065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875546 | GGCCTCTGAGCGTGT[C/T]TGAGAAAGGGGTCAG | 10451 |
rs181285840 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812737 | GTCAAGCACTAGGAA[G/T]AGGATAAAAATAAGT | 10451 |
rs181289646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107933753 | CCCAGGAATTCAAGG[C/T]TTCAGTGAGCCATGA | 10451 |
rs181292508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107840030 | AATAATTAATAACCT[C/T]CCAAAAGAAAACATC | 10451 |
rs181301490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802199 | ATTTTTGCATGTTGG[C/T]TTTGTATGCTGCAAC | 10451 |
rs181317495 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895348 | GGTACTTTTTCACAT[G/T]GCTTGTCATCTGCTG | 10451 |
rs181318575 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107688093 | TCTACCAACTTCTGG[A/C]GATAAGGGCCACCCT | 10451 |
rs181331168 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107721815 | TCAGCTTCCTCCAGA[C/T]CCAGCATGACTGAGG | 10451 |
rs181338850 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107753778 | TTGGTCAGTCTGGTC[C/T]TAAACTCCTGACCTC | 10451 |
rs181339287 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107635133 | GGGTATATACCCAAA[G/T]AATTATAAATCATGC | 10451 |
rs181340788 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591198 | CTTCTTCAAAAAGCC[C/T]TTCTCTGACCCTGAA | 10451 |
rs181351732 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107744613 | AAACAAACATTTTTT[C/G]CCATTAAAAGTAATG | 10451 |
rs181354209 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107763076 | AAGAAGGCAGAAAGA[C/T]ACCAAGAATAAGGTA | 10451 |
rs181361300 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780721 | CAGTTTCGCTATGTC[A/G]GCCAGGCTGGTCTCG | 10451 |
rs181371222 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107856788 | ACACCTGTAATCCCA[A/G]CACTTTGGGAGGCGG | 10451 |
rs181381904 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947594 | CACTCCATAAGAAAG[A/G]AAATTAATATGCTGA | 10451 |
rs181393313 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821752 | CTATGGAAATAGATT[G/T]CAGGAAGGCAAGAGC | 10451 |
rs181394079 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107586018 | GTGATGAACCAGCTT[C/T]CTGCTACGCTACCAG | 10451 |
rs181401371 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107669568 | CTCGGTAGCTGATGG[A/T]TGTAAATAAAGGTAG | 10451 |
rs181408288 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107708060 | TGAGTAACTACCATA[C/T]GCACAAGCCCTTGGG | 10451 |
rs181409224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107629371 | TATGAACAATTTCTT[C/T]CAGCATGAAGGATAT | 10451 |
rs181419962 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107654875 | TAATGAAATAGTACC[C/T]ACATTCTAAAAGTAT | 10451 |
rs181427960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107607152 | GTAGAGATGGGGTTT[C/T]ACTATGTTCCAGGCT | 10451 |
rs181435960 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107673430 | TCTTGGAGCTGTTCC[C/T]TCTGCCTGCAACCCT | 10451 |
rs181449647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107735524 | AAATGATAAAGGGGA[C/T]ATCACCACCGATCCC | 10451 |
rs181473155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107770427 | TGTTGTATTTATTAC[C/T]ATATCCTTAGTCCCT | 10451 |
rs181474074 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107918747 | TTTTGCTCTTGTTGC[C/T]CAGGCTGGAGTGCAA | 10451 |
rs181482112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107929399 | AAAAGCTAAGGAATT[C/T]CATCAACACCAGACC | 10451 |
rs181490944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107901795 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCAA | 10451 |
rs181499535 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107880562 | ACACTTCAGGAGGCC[A/G]AGGTGGGCAGATCAC | 10451 |
rs181501104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860587 | CCCTTTCTTTAAATG[C/G]CTTCTATTCTCTCCT | 10451 |
rs181504765 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107956783 | GAGAGCAGTCAGCAC[A/G]GTGCGGGTTTTCCTC | 10451 |
rs181508494 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107891929 | AGGTAAACTTGAAAG[A/G]TAACCTATCCCTTTA | 10451 |
rs181509415 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107797216 | TTACCCAAGCAGTCT[A/C]ACATACAGTCAGTAT | 10451 |
rs181511014 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107843450 | TGGATTTCTATCACA[A/T]CTCTAAATGTTCACT | 10451 |
rs181520597 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107806667 | CACCAGTTTTCTTCA[A/T]ATGAGGTGTTGCTCA | 10451 |
rs181522207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597206 | TGTTTCTATTGGAGC[A/G]CCTTTTTAAAAATAA | 10451 |
rs181529419 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107816697 | TTTTAAAGTAATAAA[C/T]TCTCGTTGTAGATAA | 10451 |
rs181536978 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107703707 | TCAATGTCCACCTTT[A/T]CCTTTGGGAAAATCA | 10451 |
rs181543213 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107718532 | TTCAAGGAGAACTAC[A/G]AACCACTGCTCAACA | 10451 |
rs181545898 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107733091 | GGTGATACCAAGGAA[A/C]ACAGGGTCTGGAGTG | 10451 |
rs181548495 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107748511 | AGCCAAGATTCAAAT[A/G]AGCGAGTTAAAACAG | 10451 |
rs181561288 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107782946 | AATAGGAAATTCTGA[C/G]ATACATTAACTCCCA | 10451 |
rs181621295 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107643112 | AACTCTATCCTTTCT[G/T]CCTATTACTTTCCTC | 10451 |
rs181624946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107682977 | AACAACTGAACGTTT[C/T]CTGCAGACAAATAAT | 10451 |
rs181631853 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908774 | AGAAAAAGCAGTTGT[A/T]TTTTAAAATTTACAT | 10451 |
rs181636884 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107871782 | ATAAATCTCCTAAAC[C/T]CCAAACAGAGGGAGA | 10451 |
rs181642711 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710552 | TGCTAAACAGTCTTA[C/T]TTTTATTTATTATTA | 10451 |
rs181643606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107938130 | TCAGGGCTATAGGTA[C/T]TCTTGACCCTTCATA | 10451 |
rs181647393 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107576571 | CACTTCTTTCCTATC[A/C]CCATTTCTAAATGAA | 10451 |
rs181661245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107835761 | ATCTGCACAGCCACA[A/G]CATCACTGCTCTGCC | 10451 |
rs181671322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913418 | TTGAAAGTACACTGC[C/T]AATCGCTCACAGCAA | 10451 |
rs181681309 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895678 | GGTATTATTGGCCAC[A/G]TCACTGATTTCTGTA | 10451 |
rs181696848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107876527 | GTTCCCCAAATGTAG[C/T]CCTGATTAGGTGAAG | 10451 |
rs181698674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592214 | TGAAGGTTTTAGAGT[A/G]TAGACCAATTATTTT | 10451 |
rs181700861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664975 | GATCTCTGCTATTGC[A/G]GGAGTAGTAGAAATA | 10451 |
rs181702804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618524 | TTAGGTTGGTGCAAA[A/G]GTAATTGTGGTTTTT | 10451 |
rs181705578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693246 | TCAAGTTCAGGGAAA[A/C]GGAGAGTGGAACTGC | 10451 |
rs181707464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107614724 | ACAGCTAGGGACTTG[C/T]ATTTGCTTTTTCACT | 10451 |
rs181707738 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107840622 | GTGCTCAAAGTTAAC[A/G]TTCTTAACGTGCCCT | 10451 |
rs181710854 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822309 | TTGCATTTCCAAAGG[A/G]ATAAGTGGGAAGTAA | 10451 |
rs181718082 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571519 | ATACCATCCACAGGA[A/G]TGTTTCTGCTTGTGT | 10451 |
rs181719652 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107803178 | CTGTGGTCTCAGTTG[C/T]TATGTCGCCTTTCTT | 10451 |
rs181722713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636208 | GGATTATGGCCACAA[C/T]AAACCATAAGATTCT | 10451 |
rs181730104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107707630 | CAGCACAACGACTTA[C/T]ATGCTCAGTGTCCTT | 10451 |
rs181734555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659667 | GTCATATTTTTTAGG[A/C]AATGCCTACTGAGCT | 10451 |
rs181741972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699412 | CTCTGCCCCTATGGC[A/G]TTGCAGGGTACAGCC | 10451 |
rs181743575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721539 | TGGGTGCTTGTAGAG[A/G]CAGCAGAGAAACACA | 10451 |
rs181748356 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107735107 | TGCTCCTGAATGACT[A/C/G]CTGGGTAAATTAAAA | 10451 |
rs181748386 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107678046 | AAGGTAGTCCTGAAA[A/G]TGACTACAAGAAGAT | 10451 |
rs181759485 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753415 | CTTCTAATTTGAAAA[G/T]AATTAGAATGGCAAA | 10451 |
rs181816693 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107934207 | GAATAAGGATAAATT[A/C]TCTATTCTGTGAAAT | 10451 |
rs181845273 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107904948 | CATGAAGGTGACATT[G/T]AAGCAAATGCTTGAA | 10451 |
rs181862397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107863984 | TTCTCTCTAAAAGTT[C/T]AAAATTTTAAGGGAA | 10451 |
rs181867366 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107622758 | TCAGAGCGACTGTCA[A/C]CCTGCCCAGTCACTT | 10451 |
rs181877185 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107829906 | TTCCCACAAGCAACC[A/G]AGAGATAAGATATCT | 10451 |
rs181878854 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107669116 | CGGTGTTCTTTAAAA[C/T]TGAAGACAGAAAAAT | 10451 |
rs181887805 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107869684 | GGTTCTGTGGGAACA[A/G]GTGGTATTTGGTTAC | 10451 |
rs181890162 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107791862 | ATCTCACAAAACCCA[C/T]GATTTCTGTATTTTC | 10451 |
rs181891011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107851526 | TTTATACTGAGCCAC[A/G]GAACAAGATTTTCAT | 10451 |
rs181891958 | snp | A/G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107938598 | AAGTGCCCAGTGGAT[A/G/T]ACTTGGTTGTCCTTT | 10451 |
rs181898386 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107834247 | ATGATACACCCGTAA[A/T]TTATTCCAAAACCAC | 10451 |
rs181903327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815325 | TGGGAGTTAGTGAGG[A/G]GAAAGGGATGTAGAC | 10451 |
rs181904735 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107919046 | ATTCTCCAATGTATG[C/T]TTTATTTACCATTCA | 10451 |
rs181906604 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107795753 | GAAACAGAAATGTGA[G/T]CTGATGTGAAGAGCC | 10451 |
rs181909790 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107597058 | TCTGAATCTCTCTAC[C/T]GTAAACTGAAACTGA | 10451 |
rs181913134 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902250 | TGCCTAGTTTTCTGT[C/G]CTAAGTTTCTAAAGT | 10451 |
rs181920170 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728755 | AGCAAAAAGACTGCT[C/T]AGCTAATATAATCTG | 10451 |
rs181924308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107642220 | GATACAGGTCATAAA[C/G]ACCTTGCTGATAAAA | 10451 |
rs181933110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761720 | TACTCTCTCTCTGTC[C/T]TGTGGGTCTTTTAAT | 10451 |
rs181935194 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107663912 | TATGATGCTGTGGGT[C/T]TGAAATCTTTTATTA | 10451 |
rs181936813 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587543 | AATTAACTGCATTGA[C/G]ACCAGTTATGTATGT | 10451 |
rs181943709 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107739004 | TGAAAGGCTCTGTTA[C/T]AAAGCCTCAGGGAAA | 10451 |
rs181946166 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107702701 | TAATGCCATACTTGC[A/G]TATTATTTTAAAGTT | 10451 |
rs181946371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107682632 | AACTGGCAATGCTAC[C/T]ATGGGTGTGGTTTCA | 10451 |
rs181949418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757990 | GTCCCGGACTCATCC[A/G]TCCAACTAAATGGTT | 10451 |
rs181957186 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107717852 | GTGTTAAAGTTTCCC[A/G]TTATTATTGTGTGGG | 10451 |
rs181957928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774722 | GCTTTCTCCCCAACT[C/T]AGGAAACAATGATTG | 10451 |
rs182061627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107954180 | AATAATAGCTAACAA[C/T]AGGTTGTCTGTGAAT | 10451 |
rs182082707 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880879 | ATTGGTGTTGTAGTG[A/T]TGTTTCGGTGCTTGC | 10451 |
rs182096541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107889360 | TTTAACACAGAAATG[C/T]AATGGCATGAAGAAT | 10451 |
rs182104204 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573226 | GATGTTGAACAGCCA[C/G]AAATGCAGCTTTTTA | 10451 |
rs182107377 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624647 | AATGAATGTTTTTCT[A/T]TCCTTGGCAATTTTA | 10451 |
rs182108625 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107887643 | CTTTTACAATGCATG[A/C]GTCTTAATTTTCAGT | 10451 |
rs182110326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107866782 | GAGCCGAGATTGTGT[C/T]ACTGTACTCCAGCCT | 10451 |
rs182114680 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107849019 | CCAACTTACAAGGGA[C/T]GTGAAGGACCTCTTC | 10451 |
rs182118832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897494 | AGCTGAGAATGCCAC[A/G]AGGGAAGGAAAAGGA | 10451 |
rs182121012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600669 | CTATTGCTTTCACTA[C/T]AATCACAGCTTTTAC | 10451 |
rs182123403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107575726 | TCTCATCTATGAAAT[A/G]AAATGTTTGTACTAG | 10451 |
rs182124767 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107647711 | TTTGGGAATCACATT[A/C]TTGTGGGTACATGTG | 10451 |
rs182126325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107609738 | ACTCGCATGCACACA[C/T]ACCCCCCTCGCAGAT | 10451 |
rs182126878 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847134 | CACTCAAAACCACAC[A/G]ACTACAAGGAAACCA | 10451 |
rs182127787 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107832773 | TTTTAAAAACAGTAA[C/T]GCTGTAGAAAATGTA | 10451 |
rs182127992 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107844801 | AGAAAGGCAGCCCCC[A/G]AAGTCAGGGGCTTAT | 10451 |
rs182130048 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594230 | GAAACTCCTCCAAAC[C/T]AGACTTGCCTGAGTT | 10451 |
rs182133148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107813709 | GAACTTACTCCTTCT[A/G]TCTAACTGTATGCTT | 10451 |
rs182135419 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107615721 | AAGGTCTAATATCCA[A/G]CATCTATAAAAAATG | 10451 |
rs182137939 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107687382 | ATGTTGGATTAAAAA[C/G]ATACTAATATCACTT | 10451 |
rs182139446 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794651 | TCTGTTACTTGTGGC[C/T]TTAAAATCCTAAAAG | 10451 |
rs182147927 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107807562 | ACTGCACTTGGCCTT[A/G]TGCAATGTGCACATA | 10451 |
rs182153067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655179 | AAAGCAATCCTGGAC[A/G]AATGGAATAAAGCTG | 10451 |
rs182157811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107811985 | AGTGGACAAATTAAG[C/T]ATGCCACACCTCACA | 10451 |
rs182177744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694963 | TAAAGCCCAGGCATT[A/G]GGAGTGTCAGAAAAG | 10451 |
rs182186202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747710 | TTACAGATGAGGAAA[C/T]TGAGGCTGTGAGAGG | 10451 |
rs182193228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726064 | GAAAGATTTTAATAT[C/T]ATGCTATCAATATCC | 10451 |
rs182195652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107715353 | ACTGTTATTGCTATC[A/G]TAAGTGACAAACATT | 10451 |
rs182202809 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107744014 | AATGTGATTTGTGGA[A/G]CTTAACGGCTACATT | 10451 |
rs182204018 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107782428 | TCTATTAGTTTAGTC[C/T]TGAATTGAATGTGTT | 10451 |
rs182219959 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107780313 | AATTTAATTCTGAGT[A/G]TTTTCAGAAAAAGTT | 10451 |
rs182281067 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107737096 | CCTGACAAAAAGAAG[A/G]AATGGTGGAAGGATT | 10451 |
rs182285813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781189 | CTTTACTAGCCTCTG[C/T]AAAATGCAGATAATA | 10451 |
rs182292401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755792 | AAACAAAATATACCA[C/T]AATAGAGCAACAAAA | 10451 |
rs182298338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107773287 | TGTTTTACCCACTCT[A/G]TCATACTGCCTCCCA | 10451 |
rs182300476 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107845091 | GTGCCCCTCTGGGAC[A/G]AAGCTTCCAGAGAAA | 10451 |
rs182305847 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107826602 | TTCACTGGCAGACAG[C/T]TGGCAAACTGATGAA | 10451 |
rs182309272 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107576980 | CAAAAGGAGAAAAGT[A/G]CAGTTAGAAATGAAA | 10451 |
rs182336843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597336 | TCCCCAGACAAATCA[A/G]TGAGTCCAAAAATCA | 10451 |
rs182338734 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107644138 | AGAGAACTCCTCTCA[G/T]TTAAATGTTTAACAG | 10451 |
rs182342247 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107619544 | AAATATAAAGGAGTG[C/T]GGTAGGAACCATACA | 10451 |
rs182346161 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107948680 | GAAATCCCATCTCTA[C/T]TAAAAATACAAAATT | 10451 |
rs182348166 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107909581 | CCATCACATACAGCA[C/T]AGAATTGACAATTTT | 10451 |
rs182358011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107930098 | GGGTACAAAAAAAAA[C/T]AGAGTAAGATATACT | 10451 |
rs182370683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893094 | TTGCTAAAGCTCCAG[C/T]GTCAACTTACAAAAA | 10451 |
rs182376699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107872465 | ATTTAATTAAATCCT[A/G]CGGAATGGAGGAAAA | 10451 |
rs182389595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860823 | ACTGCTTGTGCCCAG[A/G]ACTTTGAGTCCAGCC | 10451 |
rs182404835 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857718 | AATGCAGAATGAAAG[A/G]GGGGGAAGTTATCGA | 10451 |
rs182428846 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107630817 | TCAAAGGATCAACCA[A/G]TACATGATTCCACAT | 10451 |
rs182435869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673937 | ATAAACTTTACAAAA[G/T]GCAAAACTCTAGCAA | 10451 |
rs182436770 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822982 | AAAATTTTGGATGAG[A/T]GAATACTAGGAAGAC | 10451 |
rs182441600 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107732266 | ATGACCGAATAGGAA[C/G]AGCTCCGGTCTGCAG | 10451 |
rs182442941 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711981 | GTGAGCCACCGTGCC[A/C]GACAACGCATTCAAT | 10451 |
rs182456010 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107766019 | CGAATCTAATACTCC[A/T]AAATAGAGTGTCATA | 10451 |
rs182467597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107602019 | AAAATGAACCTAAAT[A/G]TTAGACATATTTTAC | 10451 |
rs182494302 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107638679 | AGTTGACAAGGTGAT[C/T]GCAAAATTCATTTGA | 10451 |
rs182496558 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107696251 | TACAACCAAATCAAG[A/G]TAATTAGCATATCTA | 10451 |
rs182503896 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107675443 | CAAATCCAGATCTGT[A/G]CCACTGTAGAACCCT | 10451 |
rs182506030 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107679925 | ATTCAAAAGAGCTAC[C/G]AGAATTTGCATCTAA | 10451 |
rs182507551 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713454 | TGCAATACACAAGTA[C/G]CATTGAAAGTCCATA | 10451 |
rs182511110 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107823492 | TCCCCACGTGGGCTG[A/G]GTAGCATTAAAAAAA | 10451 |
rs182518900 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107804579 | TTTTCTCAATTTACA[A/C]ATTTTTGTATTGACT | 10451 |
rs182521099 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107726692 | TAGACTACCAACCTC[A/G]TTTCCTTTATTAAGA | 10451 |
rs182531651 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107740167 | TGTTGCGTGCCTATA[A/G]TCACAGCTACTCAGG | 10451 |
rs182534515 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107716394 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGGATCAC | 10451 |
rs182534729 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107759121 | CTTGGCAGCTTATAC[C/T]TCATTTTTCCTTTCT | 10451 |
rs182543824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776534 | TGTAAAGGTCACAAG[A/G]CTAAAACAAGCCCAG | 10451 |
rs182546655 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107745694 | TAGAGGCTTAACATA[C/G]TATTTTAAGTGCCTT | 10451 |
rs182588268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945390 | TGTTTACTGCTACTA[A/G]TAACAGTTATTATAT | 10451 |
rs182598584 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107907062 | GAATTTTTATATCTC[C/T]ACAACAACTTTCTGG | 10451 |
rs182604912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107926270 | TGGGTGGCAGAACGA[A/G]ACTTGGGTCTCAAAA | 10451 |
rs182615837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906571 | CTCGGGAGGCTGAGG[C/T]GGGAGAATGGCGTGA | 10451 |
rs182638010 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107876925 | CCAATGTCTTAATTC[A/G]TTGTTTTGTTTATCT | 10451 |
rs182659777 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107841064 | TGTGGTAGGGCAGAG[C/T]TGGCCAGTACCAAAG | 10451 |
rs182678527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107838122 | ATGGAAGAATATATT[C/T]GCAAACTATGCATCC | 10451 |
rs182682302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107803927 | TTTGTGTGCTTTAGT[A/G]TTGGATGCATATTTA | 10451 |
rs182703036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939331 | TGGTCCTAGGCTTAC[C/T]ATGGTTCAACTTACA | 10451 |
rs182707678 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107604204 | AATAATTAATGTATC[C/T]GAAAATCCTCTGATT | 10451 |
rs182708986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107582289 | CCTGGTTTTATTTTA[A/G]AACTCAGGCATATCG | 10451 |
rs182715451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107920964 | ATAAAATAAAACTTA[C/T]TAGTATTTTAATTAA | 10451 |
rs182719599 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107584760 | GTATTCAATGCTACA[C/G]AGTATAAACATATAA | 10451 |
rs182721933 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588440 | ATGAGGCTAATGTAA[A/C]ACTTCACACTGGGTA | 10451 |
rs182722299 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107651799 | TAAATTATATAATAA[A/G]TTTCCTATTAAAAAC | 10451 |
rs182726027 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107882742 | TTTGTCCTTTTCCCC[C/T]GTGTATCAGTGGGTC | 10451 |
rs182729093 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107679100 | TGGTAATGAAAGAAA[G/T]ATTTCTTAGATTCCT | 10451 |
rs182730417 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903457 | TATGAGGGCTGTGGC[A/G]GCAGAGAGACCTGCA | 10451 |
rs182734058 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107627348 | AATCTCTTCAGAATT[C/G]ATCATTTGCATTTTT | 10451 |
rs182734261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716251 | AAAGAACTTTAAAAC[A/G]TTAAATGTGTTTATT | 10451 |
rs182734397 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107671227 | CTGAAGACATCACAC[G/T]ATTTTGTTGGGGCAT | 10451 |
rs182735764 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107700635 | AAGGACATGATCTCA[C/T]TCCTCTTTATGTCGG | 10451 |
rs182741943 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107862448 | TAAACATGGAAAGTG[C/T]CATCCTCCTTTTCTA | 10451 |
rs182743167 | snp | A/G/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107845260 | AGCGTCAACATCAAC[A/G/T]AAAAGGACGTCCACA | 10451 |
rs182744190 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632264 | ATCTACTTATGCCTG[A/G]GCTCAACCAAGGCCA | 10451 |
rs182751773 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107729437 | AAGTCTATAGTTTGG[A/G]GTTAGGAGATAGAAA | 10451 |
rs182753724 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107665496 | ACTTTTGTGTGAAGG[A/G]TTCTGCACTAAATCT | 10451 |
rs182754313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107827123 | AGTTTTATCTACCTG[C/T]TTTCTACCCTGAACT | 10451 |
rs182766648 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107661531 | TTGTTTTGCTTTCTC[C/T]CCACTTGAATATAAG | 10451 |
rs182772401 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107700799 | AGAATGATTTCTATT[C/T]CTCTGGGTATATGCC | 10451 |
rs182789596 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729870 | TTTAGTCAAAAATTT[A/T]ATTTTAGAGATCATT | 10451 |
rs182831949 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107764111 | AAAAACAAAACAAAA[A/C]AAAAAACATGATGTA | 10451 |
rs182860543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720128 | GATGAGTTAATAGGT[A/G]CAGCAAACCAACACA | 10451 |
rs182863782 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107733839 | ATTAACCAGGAGGAC[A/C/G]TCCCCAACCTAACAA | 10451 |
rs182875266 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107751675 | AGTACAGAAAGGGGC[G/T]GGGGGGCGCGCGCTA | 10451 |
rs182880053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767936 | CAATTAAAATAGTCT[G/T]GTAAATCATAAGGAA | 10451 |
rs182891366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107961893 | TTTAAATGCAAACAA[A/G]GCAGAAGGCTAACAG | 10451 |
rs182901114 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107955159 | TAGGTTCTTTTATTT[C/G]GTCTATTTTAGAGAT | 10451 |
rs182927168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587737 | CTGGGATTACAGATG[C/T]GTGCCACCACACCGG | 10451 |
rs182932080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107916437 | TTTATTTTGAAGGTG[C/T]AGTTTCAAACCTCAA | 10451 |
rs182935354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107610649 | TTCACATAGAGCTTC[A/G]CACAAGGAAAAATAT | 10451 |
rs182936493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107936002 | AGATGAGGACACATT[C/T]ATGCCCCTTTTGGAA | 10451 |
rs182937724 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107914957 | GAAAACTAAAGGGAA[G/T]AACTCATTTTTTATT | 10451 |
rs182939802 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107877958 | AGGAATAGAGGAAGT[A/G]AGGCTGCCAGCCTGC | 10451 |
rs182944805 | snp | A/T | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966133 | ATTATTTGTGGCAAG[A/T]TATTGCCACAGTGAA | 10451 |
rs182945005 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107944207 | CTGTGGCTTAAGGAT[A/G]CCGGACCCCCTCTCA | 10451 |
rs182945919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107854831 | GAAAGCATAACAGTA[A/G]CTGCTGTAACAAACC | 10451 |
rs182948158 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107898969 | TCTGAGTACTAAGGA[C/T]GTAGAGATGAACTAG | 10451 |
rs182951760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107631314 | CTAAAATGCAGGCAT[A/G]ATACATGTTTAGCAG | 10451 |
rs182955910 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107878383 | TCCAGTCATGTTTTA[A/C]CCACTGCATTTGGCA | 10451 |
rs182956054 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107858878 | TCTTCAAATGTTCTT[G/T]AAACTATACAGTTGT | 10451 |
rs182958153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107674994 | AAAGGAATGGAATCC[C/T]GCGAAAAGCAGTGTA | 10451 |
rs182965201 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107655865 | TCTCAATATCAATAA[A/C]CATCAGGGAAATGAA | 10451 |
rs182967161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841368 | ATGGGGAAAAAAACT[A/G]AAGCAATATAAAGGG | 10451 |
rs182969874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107695485 | GTTGACACCCAGGTC[C/T]ATGTGAGTGTTTGGA | 10451 |
rs182970177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107842490 | AACTGGAAATTGTTT[C/T]GGTACTTCCACCCAT | 10451 |
rs182971814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824220 | AATGCCAGATTGGAA[C/T]AGACTGAAAAACAAA | 10451 |
rs182980071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805257 | TCTTTCTACTCCTCG[C/T]TCTTCTTCAACTCCC | 10451 |
rs183037159 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107611769 | ACTGAGGCTGTTCCA[A/C]CCTGGTGTCCCACTA | 10451 |
rs183038446 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107616640 | AACAGAGTAACAGAC[A/G]CTTTTCTATTCTCTT | 10451 |
rs183042318 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107656235 | GGGTGGATAAGAAAA[C/T]GTGGCATATATACAC | 10451 |
rs183046365 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107615208 | AAGCTGACAAAAACA[A/G]GCAATGGGGATAAGA | 10451 |
rs183047768 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107660479 | ACAGAAAGAAAGACG[C/G]AAATACGCACCAGGC | 10451 |
rs183050928 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107683347 | TTACACGTTAGACCA[C/T]GACCTCCTGGTCACA | 10451 |
rs183054913 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107639659 | ACCTGCTAGAATAAA[A/C/T]AAAATTTAAAAGACT | 10451 |
rs183064965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662865 | ACTTTCACAATGGGG[C/T]AGGTGTCAATCAGAA | 10451 |
rs183078734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107701389 | TGGCTGGAGCAGCTG[A/G]GAACACAGGGCACCA | 10451 |
rs183080010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107681702 | CTTTGTCACCAGGCT[A/G]GAGTGCAGTGGCGCG | 10451 |
rs183086333 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107716597 | GCCCACTTGATCATG[A/G]TGGATAAGCTTTTTG | 10451 |
rs183087938 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736849 | CACAGAATTAGAAAA[A/G]ACTACTTTAAAGTTC | 10451 |
rs183094109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755012 | ACTGTCTCCTCAATC[C/T]TGAGACCATCTTGTT | 10451 |
rs183094482 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690336 | AACAATGGTATTTAC[A/G]GTGGTCAAGTAGCTA | 10451 |
rs183095687 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107730499 | CAAACCGTTGCATTA[A/C]TCATATAAGGCTCAA | 10451 |
rs183098501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771562 | CCGGCCTGTTGTTAG[C/T]TTTTCTAACTGTGAA | 10451 |
rs183104330 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107790317 | AATGGTCACCCACCT[A/G]GAAATTCATCACCTA | 10451 |
rs183104493 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107723724 | AGGAGCTGTTCCTTC[C/T]AACCTCCAAAACAAT | 10451 |
rs183119550 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755669 | CAGTCAATCAAAGCT[A/G]CATCACAGAGGCAAT | 10451 |
rs183134226 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790552 | GGTTCCAGGTAAGTT[A/C]TCTGAGGGACAGGGG | 10451 |
rs183169582 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940515 | AGTCCTCCTGGTTTC[A/C]GCCTTGCCAGGATGC | 10451 |
rs183171536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959715 | CCCAGTCTCATGATT[C/T]TAAATACCATCTTCA | 10451 |
rs183182196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921584 | CTCAAACATGAAACC[C/T]GCCTGACAGCCAAGT | 10451 |
rs183201461 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107935363 | TTCACAGTGATAAGG[C/T]ATATCAAAGAAGTAA | 10451 |
rs183204104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107958982 | AAACTATATCTAGGC[C/T]GGGCACAGTGGCTTA | 10451 |
rs183206043 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107930432 | AACAATAGAAAGTCT[G/T]CCCCTCCCCTCCAAA | 10451 |
rs183218953 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897773 | ATACTCTTCCTTCAT[C/G]TATGGTGCTAGAATC | 10451 |
rs183235793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893381 | AGTGTTTACTTAAAA[A/G]TAATCTACTTTTACA | 10451 |
rs183240112 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107855355 | AATCATGGCTCACTG[C/T]GGCCTCAACTTCCTG | 10451 |
rs183240640 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107858069 | TGTAATAAAGAATAT[A/G]CTTATACATTTTATA | 10451 |
rs183268483 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620612 | TGTCACTTTTTTTTT[A/C/G]TTCACACAGACAAGC | 10451 |
rs183275919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107644434 | CTTGTTTGGTAGACT[C/T]CCTGGGTAATTTTGT | 10451 |
rs183282238 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592964 | TCTTTCATGGAGTCA[A/C]TGAAGTTTCTAGAGG | 10451 |
rs183290000 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107793311 | ACAGCCTGTCATGAA[C/T]GCTACATAAATTGTA | 10451 |
rs183315315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107637482 | ACAAAAATTAGCCGG[A/G]CATGGTGACGTTCAC | 10451 |
rs183325993 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107666127 | GCCCTTCACCTTACC[A/C/G]TTCCTCTTCACTGTA | 10451 |
rs183330251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107892228 | ATAATATGGGGAAAA[C/T]TACGTTTTCCTTAAA | 10451 |
rs183346074 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107871845 | ACAATGAGAAAAGGG[A/G]TAAGAGAGTATAGCT | 10451 |
rs183346243 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107685013 | CTTAATGCACAATAG[A/C]AGCTGTCTTTCTACT | 10451 |
rs183348796 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107598940 | AACTTGAAAGGAATT[A/C]TAAGCCATAGCTTTG | 10451 |
rs183350700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107854209 | CAGTTACTCTGGAGG[A/G]TGGGACATGAGAATC | 10451 |
rs183354127 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107705737 | GACAACCATATGACA[C/T]TCATTTCTTCATTTA | 10451 |
rs183354668 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107837179 | ATCCTTAACAAAATA[C/G]TAGCAAACCAACTCT | 10451 |
rs183355624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107719237 | TAAAGAGCTTCTGCA[C/T]GGCAAAAGAAACTGC | 10451 |
rs183358765 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107645935 | CAGTCATTGTTGCAG[A/C]GTTTATTAATAAGGT | 10451 |
rs183361025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107733605 | TCATACACAAGCTTC[A/G]GTAGCCGATTCAATC | 10451 |
rs183365825 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107709093 | ATTCAGATACGTCAG[C/T]CTCCATAACACTTTA | 10451 |
rs183366822 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818296 | CTAATCAATCAGTAT[A/C]CACATGGAGCTCTAC | 10451 |
rs183370989 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107736892 | AAAAGAGCCCGCATT[A/G]CCAAGACAATCCTAA | 10451 |
rs183371761 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107685814 | CATTCTGTCATCTCT[A/G]TGCGTATACTCCCCT | 10451 |
rs183373066 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107797609 | TTTAAAGAATAGTTA[C/T]TAATGGGTTATGTAG | 10451 |
rs183373547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107712624 | TGCAAGGACTTGGTA[C/T]GTGATTTTTGTGGCA | 10451 |
rs183389168 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107739673 | AAAACAATCCAAAAG[A/G]GCTGACAAATATACA | 10451 |
rs183390851 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107772645 | CAAAGGTTAAAAAAA[A/T]TCCCAGCAGATGTTA | 10451 |
rs183411630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107775202 | GGATTTATCCTGACA[C/T]CATGTCTGCCTAAAT | 10451 |
rs183430180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950169 | TAGTGTCCAACTTCT[C/T]AGAATCAAAGTTCTC | 10451 |
rs183463454 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107909921 | TTCCAAATCGGTTAC[A/G]GGTTATTTGAACAAT | 10451 |
rs183468737 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107795982 | CTAATTCTCAGAGTT[G/T]AAGAAGATTGGGTAA | 10451 |
rs183490381 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107838537 | CTGTGGAGAGCAGTT[A/T]GGAGATTTCTCAAAG | 10451 |
rs183513248 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107809356 | TAACATGTTCAACAA[A/G]GAAGATCACATTTCC | 10451 |
rs183514023 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107760186 | TGACAGACTAATACA[C/T]TAAGACATTTCTTTG | 10451 |
rs183519556 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107906254 | CCAAGGCTTGTTTTG[C/T]TTTGTTTTGTTTTGT | 10451 |
rs183519960 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107776692 | TTCCTTGAGGAGTAA[C/T]GATCACGCATATATT | 10451 |
rs183540928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107866062 | TACTGGGCTTGCAGG[A/C]AACCCACCCTAAAGG | 10451 |
rs183575077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794204 | CCCTGAACTGGTATC[A/G]GGCAAGATCCACAAA | 10451 |
rs183575643 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107621544 | ACTGTAACTATGACA[C/T]AGACCAACCTCAAAT | 10451 |
rs183578966 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107577886 | TGTACCATGGCCTAA[C/T]CTGAACTGTGACAAA | 10451 |
rs183598099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107626177 | ATTAACAATTAGGAC[C/T]TCACCCACTTTGTCA | 10451 |
rs183605327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107583275 | GTTTGAGTAAGAGCT[A/G]TCTGTGACAAACCCA | 10451 |
rs183606276 | snp | C/G | 0.00679956 | 0.0579098 | intron-variant | VAV3 | GRCh38.p7 | 1:107726551 | TGTAACATCAAAAAG[C/G]CTTCTTCACTAAAAG | 10451 |
rs183608296 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107666797 | AGTATATATTAACTC[A/G]TTTAAGCCTCATGAC | 10451 |
rs183626985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107706740 | GGTTCATTTGTTTCT[A/G]AGCATCAAGGTGATA | 10451 |
rs183632009 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107932781 | TTACAGTGATGTGAT[C/G/T]TGAAGGATAAAGAAG | 10451 |
rs183633316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107758831 | CCCAGACAACTTATA[C/T]TCTATTCATACTAAA | 10451 |
rs183634484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107670405 | GGCATTCTCAGAGCA[C/T]GTTAAATTTACATAA | 10451 |
rs183638716 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107952241 | ACATGTTCTCACTTA[C/T]AAGTGAGGGCTAAAT | 10451 |
rs183641272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911135 | CAACTTCTAATAGCA[C/T]ATAAGGTTAGAAATT | 10451 |
rs183642245 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107708689 | CTCAAATGCAGCATA[C/T]ACAAAACTCAACTTC | 10451 |
rs183655825 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894572 | AAATCTTGGCAGGCA[A/G]CTCCCAAAAAGAAAA | 10451 |
rs183698074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107764663 | AGGTAGCTAGAACTA[C/T]AGGCATGAGCCACCC | 10451 |
rs183715673 | snp | C/T | 0.000495491 | 0.0157321 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107596340 | TAGTACTCCACAAGT[C/T]CCTTTGGAAAAAAGA | 10451 |
rs183720497 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107955721 | GACATTTAACAGCAT[A/C]GTCTTCAAGAAACTG | 10451 |
rs183724187 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107618080 | ATGCGCAGTTCACAG[C/T]CAAGTCTGCGCTCCT | 10451 |
rs183732316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107653226 | TCTGCACCATCATTT[C/T]GATGTGCTGATTTTT | 10451 |
rs183736901 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107691547 | AAAGTCTCTCTTTCT[G/T]TATCTCTCTTTTTCT | 10451 |
rs183737446 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107924944 | CCAAAAGATATGTAC[C/G]CATTCAGCAAAAGAT | 10451 |
rs183742476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107641595 | GATTTCATCATGGGC[A/G]AACATCAACATGCTC | 10451 |
rs183746120 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107672047 | CCAAGGCGGGAGGAT[A/T]ACATGAGGCCAAGAG | 10451 |
rs183759233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709303 | AATGCTAGATATTCA[C/T]AGCTGATAGAAATCA | 10451 |
rs183763717 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107724483 | GTACTGGGACAAAAA[A/T]TACATGGCCTCTGGC | 10451 |
rs183766442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888741 | TGGGATTACAGATAT[A/G]AGCCACTGGGCCGGG | 10451 |
rs183776077 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107848433 | AACATATGAAAATCA[A/G]TAAACATAATCCATC | 10451 |
rs183791234 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107813055 | ATGAACCCAGGAGGC[A/G]GAGCTGGCAGTGAGC | 10451 |
rs183800526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948123 | TTGATTTTATAATTT[C/T]CATTAATCATTTTTC | 10451 |
rs183806870 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107883415 | ACATACATGTTTTCA[A/C]ATAAATTGATGAATG | 10451 |
rs183813338 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603430 | GACACAGAGGAGTCA[C/G]TGGGTATTGGGTAAA | 10451 |
rs183823105 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107845517 | CGAACTAAAGAAGTA[A/T]GTTATAACCAAATGC | 10451 |
rs183823136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107909516 | TAAGTTTAAAAACCT[A/G]CTGAACCCATTTTAA | 10451 |
rs183843948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107810455 | TTTCAATTCCACATA[C/T]TCTATTTATATCTAT | 10451 |
rs183849387 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107714538 | AAATCCAAGTATTTA[C/T]TTTTAAAATATCTTA | 10451 |
rs183852641 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689789 | TTTCAGAAGAAAGAT[C/T]GCCCAAGAGCGCTGG | 10451 |
rs183854829 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107699024 | GCCAAACCATATCAT[G/T]CTGCTCCTGGCCCCT | 10451 |
rs183857913 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107728299 | ATGAAGAGGAATCAC[C/T]AGGGATTAAAGGACC | 10451 |
rs183858627 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107863028 | ATATAGCAAAAATCA[C/T]AGAAAAATAAAACAT | 10451 |
rs183869478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107723324 | TGCTTATGCTGTGTT[A/G]CTGCCCTTCTGTGTT | 10451 |
rs183873102 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107845816 | GAAAAGACCAAACCT[A/G]CATTTGATTGGTGTA | 10451 |
rs183874018 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107742467 | AGGTACACCAAAATA[A/C]ACAAAAGATAATTTC | 10451 |
rs183878184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760933 | TAAACATTAAAAGAT[A/G]CAAAGGCCCTAGGCA | 10451 |
rs183879282 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107828296 | TATAAAGGGCACTTA[C/G]CACCTGAAAAAAGAC | 10451 |
rs183882591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107810727 | AATAGGTAATCATGT[C/T]ACAGCAAGGCTCCAA | 10451 |
rs183884387 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107778651 | TCTCTCCCTTAGAAT[A/G]TGAATGTGAGCTGGA | 10451 |
rs183887574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107577681 | AAGCTACTATCTTGG[G/T]TCATGAGGAGGAAAG | 10451 |
rs183892116 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107791117 | ATGGACACCAAAATA[C/T]ATACCTCCTAACTCT | 10451 |
rs183902384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746095 | CAAAATTTGAACCAT[A/G]GGCAAAATCAAACTT | 10451 |
rs183924467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781509 | TGTTGCACAGATCAA[C/T]ACATATAATTTTTAT | 10451 |
rs183958374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599790 | TAAATTTAATTCCAG[G/T]CCCTATTGTGTTTCA | 10451 |
rs183970543 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107578919 | ATAAGCCAGTGAAAA[C/T]ACAGTTAAATGCAAA | 10451 |
rs183974833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107646133 | TGGCTACCATACTTC[A/G]AAGGATGCTGAGGTG | 10451 |
rs183984809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107621935 | ACAGGTTGGGTCATT[C/T]TTATGAAAATACATT | 10451 |
rs183990596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667334 | GTACACTGCTAAGTA[A/G]TGAGAAAAAGCACTG | 10451 |
rs183991944 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107696842 | CATCCCCTGGATATA[G/T]CTTATCCCTTTTCCT | 10451 |
rs183999093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750993 | TAGAAATCATGGGTT[A/G]GTCTGTCTCCTTGTA | 10451 |
rs184002793 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726895 | AAGGGACCATGCTAT[C/G]ATTGTCTAGTGTGTA | 10451 |
rs184003765 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107929707 | AAAAGTGTAGAAATT[C/T]ATTAGTTTTCTTTTT | 10451 |
rs184008821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862738 | AGCTCAGATAGGATA[C/T]GGCCCAACAACTAAG | 10451 |
rs184015956 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107785752 | CTGTAGACCAGGTCA[A/T]CTGCAAGCTAGAGGC | 10451 |
rs184022226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107827469 | GATGGATTTATAACT[A/G]GCTGAAATATCACAC | 10451 |
rs184036503 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790933 | CCTCATGATCTGCCC[A/G]CCTCGGACTCCCAAA | 10451 |
rs184062668 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107629630 | AAGAAAAAAAGAAGA[A/C]GACAAAGAAGAAAAG | 10451 |
rs184070274 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107586112 | AAGCCATCCCTCAGC[A/G]CTCATGAGTACCACT | 10451 |
rs184076206 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107607157 | GATGGGGTTTCACTA[G/T]GTTCCAGGCTGGTCT | 10451 |
rs184081164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673502 | GGATTCCAGGTTAGA[C/T]ATCATTTCCTGATGC | 10451 |
rs184087065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107925649 | CATAGGTACAAAAAG[C/T]AGAATGGTGGCTGTC | 10451 |
rs184087486 | snp | A/G | 0.0012109 | 0.0245761 | intron-variant | VAV3 | GRCh38.p7 | 1:107717154 | TTAGTCTTGCTAGCA[A/G]TCTATCTATTTTGTT | 10451 |
rs184091535 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107889661 | ACATCTGCCTTACAA[C/G]AGTAGAGTGGCAATA | 10451 |
rs184092624 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107701932 | CTTTCCCACATCTTC[C/T]TGTCTTCTTCTGAGC | 10451 |
rs184094112 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107654892 | CATTCTAAAAGTATA[A/G]TAAAAATATACAACA | 10451 |
rs184096789 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107597846 | CATGTGAAAAACTGT[A/G]ACAGCTACCCCATTA | 10451 |
rs184099914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107859814 | AAAGTAATGTCTGAA[C/T]CTTTATTCAATCATG | 10451 |
rs184100737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860239 | CATCCTCCTACCTCA[A/G]TCTTCCAAGTACCTG | 10451 |
rs184102019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107843199 | AGCTCTGGAATCAGG[C/T]TACTTGGATTTAAAT | 10451 |
rs184102756 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107731618 | TATAAGAATCTTCTA[C/T]AGTAAAATCTTCTTC | 10451 |
rs184105370 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107746702 | GACTATACGTTGGTC[A/G]GTATTATGTAACAGA | 10451 |
rs184107449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107867605 | AACAAGCTATCTTTG[C/T]TCAGGGAGGAATCAC | 10451 |
rs184108696 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825189 | TCTTATCTTTTACAG[A/T]GAATGTCTGCTGACC | 10451 |
rs184110694 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107710714 | TAGCAAGGTTTTAAA[A/C]TCATTTAAAATAATA | 10451 |
rs184111843 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107849289 | AATCCTAGGCAAAAA[C/G]AACAAAGCTGGAAGC | 10451 |
rs184115368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107764928 | CTACCATATTACTAT[C/T]TTATAGAGCTGTTTA | 10451 |
rs184116140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107806559 | GAGGGTAAGAACATA[C/T]GTTGGAATATTTGGT | 10451 |
rs184120602 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107781806 | ATCAGATAAAACTTG[A/T]TATTGATTAATTCCC | 10451 |
rs184124460 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107675594 | TTATTGCCGTGAAGC[A/C]GGTAGTGGCTTAAAT | 10451 |
rs184130540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824898 | AGAACAGGAACACTA[C/T]TTTAAGAGTAAAAGA | 10451 |
rs184159304 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107713965 | ATTTAACGTTTGTGC[C/T]GAATGTTCAAATACT | 10451 |
rs184161025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767730 | ATGGGGGTGGGGATG[C/T]ATAAACCAAAGCAAG | 10451 |
rs184164769 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107740933 | CAAAATGTTGCTGGC[C/T]CTTGTTCTAAGAGAC | 10451 |
rs184200120 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107820356 | AAGTGAAATGAGCCA[A/G]GCACAGAAAGACAAA | 10451 |
rs184205390 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107800596 | CATGGGAATATTGCA[C/T]GATGCTGAGGTTTGG | 10451 |
rs184225373 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107605357 | ATCTTTGGAGTAGGT[A/T]CCTGATAAAAAGAAT | 10451 |
rs184225792 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107944561 | TAAATGCTGAATGAA[A/T]GAAAGAATGAACTCT | 10451 |
rs184267930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842865 | TCTCCAATGAGAGAA[A/G]TATTAACATAATATG | 10451 |
rs184278602 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107805733 | TGTGGATGCATCTCC[A/G]TGTCTTTATTCCAGT | 10451 |
rs184281089 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590073 | TGACAGGAAAGAGAC[C/G]ACACCCAGGGAGAGA | 10451 |
rs184283772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107634421 | ACTGGCTAGCCATAT[A/G]TAGAAAGCTGAAACT | 10451 |
rs184290104 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612913 | ACAATCCAGTGCCTG[A/C]CTTTGAGCTAGCCAT | 10451 |
rs184294024 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962990 | TGATGCTTATAATGA[C/T]AATCTTTGGTCATCA | 10451 |
rs184296127 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107657771 | TATTAATTATAAACA[G/T]AAAACAGAACTGGAT | 10451 |
rs184301758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698285 | ATTTTGATATTTTCC[C/T]GGGCGAGCAACATGC | 10451 |
rs184307940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107675777 | CTAACATGTCAGTAG[A/G]TAACAGTAGAAAAAA | 10451 |
rs184312051 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107941276 | AGTACTAAAGGACTA[A/C]ACTGAATGTGGTCTC | 10451 |
rs184316293 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107681911 | GTGATCCGCCGGCCT[C/T]GACCTCCCAAAGTGC | 10451 |
rs184319073 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107714130 | GGAGACCAAAGGAGA[A/C]CTGAAGCTGTCTGAA | 10451 |
rs184322697 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | VAV3 | GRCh38.p7 | 1:107922665 | ACATATTAAAGAGCA[C/T]AATTTGGCCGGGCGC | 10451 |
rs184330977 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886940 | AAACACATCCAAAAG[C/G]ATTACATTAACAAAT | 10451 |
rs184333954 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107904758 | AAGAAAAATTTCTCT[A/G]CCATCATGAGACTTT | 10451 |
rs184337237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107863685 | ATATAGATACGTATA[C/T]CTTGGTATGTCTGTA | 10451 |
rs184348274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717517 | AGTCATTCAGGAGCA[A/G]GTTGTTCAGTTTCCA | 10451 |
rs184351159 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107846926 | ACCAACTGGACCTAA[G/T]AGACATCTACAGAAC | 10451 |
rs184356673 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107585300 | ACTATCATCTCTTAC[C/G]TTGATTGCTGTATGG | 10451 |
rs184357980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747219 | TAACTGTTTGTTTTA[C/T]GGCAACTGAACAAAA | 10451 |
rs184374311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782138 | CCCAGCATATATCAC[C/T]ACTTAATAACAAGAA | 10451 |
rs184390594 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107874499 | GCAGCTTTCAGATAT[A/T]GAGAAGACTGGAGGA | 10451 |
rs184397807 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107940961 | AACATGGTTAAAATG[A/G]TAAGTTTTATACTAT | 10451 |
rs184409598 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107904331 | GTCCAGCAGGCGGGT[A/G]CCAAACATGAACAGT | 10451 |
rs184411355 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107839916 | ATGCCCACAAATTTG[A/G]TAACTTAGGTGAAAC | 10451 |
rs184417434 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107628357 | ATTGACAAGGTAAAC[A/T]AAGACAAAGGCCAGC | 10451 |
rs184419998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107795343 | AACATATCCTCGGTG[C/T]TATATAAAAACTCTT | 10451 |
rs184431159 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107801553 | CACCTGTAACAATAG[C/G]TGAGTGTTGGCCAAT | 10451 |
rs184442265 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733739 | AGAAATATGGGACTA[C/T]GTGAAAAGACCAAAT | 10451 |
rs184442815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107663841 | ACAAATGATTTTCAC[C/T]TGAAGATTCTTGCAA | 10451 |
rs184449875 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702480 | GAGTAAATTGTGAAG[C/T]TAGGATTCAAACAGA | 10451 |
rs184482273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731881 | AAGGTATTCAGAATC[A/G]ATGGGAAAAAACAAC | 10451 |
rs184492762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107765069 | TAAACTAAAAATAAA[C/T]AGGCACCTCTAATTT | 10451 |
rs184496294 | snp | A/G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107585898 | ATATTTATGCAAACT[A/G/T]ATAATAGCAGAAGCT | 10451 |
rs184507191 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594888 | CAAACAGGATTTTTC[A/T]TCTAACTGACCTCCC | 10451 |
rs184514380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921828 | TATCGTTTTGATTTT[C/T]TTAATCTGTAAAAAC | 10451 |
rs184534185 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107938198 | GAAACAATTACCCTA[A/C]AGAAGAGGAGGCGAT | 10451 |
rs184534594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107856278 | TACATCATTCCAGTG[A/G]AATATCCCACATTGC | 10451 |
rs184546222 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885742 | CAGGTAAAACAACTG[G/T]CCCTACCTCACATAG | 10451 |
rs184549492 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107821232 | AAATGTTATAGCATG[C/T]GTATTCACTGATTTG | 10451 |
rs184550929 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107735212 | CATTTAAAGCAGTGT[A/G]TAGAGGGAAATTTAT | 10451 |
rs184553060 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753559 | ATATATACACACACA[C/T]ACTTTTTTTTTTGAG | 10451 |
rs184560687 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107635596 | TGCACGTTGTGCACA[C/T]GTACCCTAAAACTTA | 10451 |
rs184561115 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107769745 | TCCTTCCCCACCCCT[C/G]TAATCTTCACCATTC | 10451 |
rs184562120 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107880667 | TGGCTGTGGTGGCAC[A/C]CACCTATGGTCCCAG | 10451 |
rs184568031 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107901956 | GCTGAGGGAGGAGAA[A/T]CGCTTGAACCCAGGA | 10451 |
rs184569876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591468 | ATGAAGCAAATCCAA[C/T]GAGGTCACAGGTAAG | 10451 |
rs184570382 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788131 | TTGCCTCAATTATTG[C/G]AATAGCTTCCAATAT | 10451 |
rs184577364 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107707211 | AAATTATTTTTAAAA[C/T]CTAGAATCAAACACT | 10451 |
rs184593291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676325 | CCAATTAAAGCTCTC[C/T]TTGGGATTCTGCTGG | 10451 |
rs184598878 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107734117 | GCCAAACTAAGCTTC[A/C]TAAGTGAAGGAGAAA | 10451 |
rs184615105 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107910445 | AAATATTATATGCTA[C/T]TTGTTTTCACTAAGC | 10451 |
rs184616486 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107767969 | AGGGTATTTCATAAA[C/T]GGGAGTTACATATGA | 10451 |
rs184622930 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107894160 | TGGACACTGTTTACT[C/T]GGGCAAGAATTTTCA | 10451 |
rs184639587 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107918470 | TGTTGCAAACCAAGC[C/T]GAGGTCAATGAAGGT | 10451 |
rs184643147 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107956687 | GTTCCAGACCATACT[G/T]TGAGAACATTAAAGA | 10451 |
rs184644857 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107873499 | TGCAGGAGGAACAGG[C/T]GGAAGGATAAAAGAA | 10451 |
rs184652843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107855905 | GAAAGCTGAGAGCAC[A/G]GGCTCCTTCCACTTC | 10451 |
rs184658524 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107839338 | TATAAAGTATGTTCT[C/G]AGACAATATGGAACT | 10451 |
rs184662557 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107820672 | GACAGATGCCCCATT[G/T]ACCCTGATGTAATTA | 10451 |
rs184671000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880474 | TCTTGGCTTTGTCCT[A/C]GAAGTGATGAGGTTA | 10451 |
rs184685748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613425 | TAACTGCTCCTTGAG[C/T]AATTTCTTCAGATTT | 10451 |
rs184713278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814304 | TCTCCACATTCTCGC[C/T]AGCACCCATTAGTTT | 10451 |
rs184713723 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107658161 | TAATACAATATATAG[A/C]TAAAGAATAACAGGC | 10451 |
rs184715371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686632 | CTATAATCCTCCATC[C/T]ACACAAAACAGAGAT | 10451 |
rs184730000 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107720753 | AAGATACGTATCCTC[A/T]ACGAGCCTGCCATAA | 10451 |
rs184739761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588771 | ACTCCATTGGAGATA[C/T]TGATCTGATATTTGT | 10451 |
rs184742176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107752156 | AGGTATATAGACCAA[C/T]AGAATAGTAGAGAGC | 10451 |
rs184765473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612634 | CCTGCTCCTTTGCAT[A/C]CTGAGTAATTTTATA | 10451 |
rs184769372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963679 | CTCTGCGTCATAGAG[A/G]ATTAGTGCTGAAATG | 10451 |
rs184782102 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107718219 | CAGGGCAATCAAGCA[A/G]GAGAAAGAAATAAAG | 10451 |
rs184782397 | snp | G/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756614 | CGCTTTAAGTTATTG[G/T]CAAATATTATTTCGT | 10451 |
rs184785744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732567 | GAAATTATAACCCAC[A/G]CCTGGCTCAGAGGGT | 10451 |
rs184788517 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107937781 | GCTTGTAGTCCCAAT[A/T]ATTAACACAATATAA | 10451 |
rs184792047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943275 | GATGCTTTCTTGGTC[C/T]GCTCTTGATTAGTCA | 10451 |
rs184793345 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107773493 | CCATTCAGAGGAAAC[A/C]CACCAGTCCCCCATC | 10451 |
rs184794217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900568 | CTGCTGTCAAGATCA[C/T]TGTAAACCATGAGAG | 10451 |
rs184802652 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107747711 | TACAGATGAGGAAAC[G/T]GAGGCTGTGAGAGGT | 10451 |
rs184831541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107617297 | AATGCGTCTAATTTG[C/T]AGCTGTGGTTTATTT | 10451 |
rs184833394 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107956333 | AAAGTAAATGGTCTC[A/G]GGCAGTTCTCAAACT | 10451 |
rs184847976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107890792 | CTGCACCAAACTTAG[A/C]CATTTTTCTACCAAA | 10451 |
rs184848003 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107937227 | TATTTAAATTCAAAA[C/G]ACCACCATGACTATT | 10451 |
rs184848770 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833545 | AACTGAGACTAACAA[A/T]ATTTTAGAAATTTTT | 10451 |
rs184850955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907728 | TCTCTTGCCCTTCCA[C/T]CTTCCACCTTCCACC | 10451 |
rs184853939 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107779696 | TACTTAAAGTAATAA[A/G]TTACTTTATTACTTT | 10451 |
rs184860750 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107917560 | CTGATTGACTAAAAG[A/C]ATGATGATACCACTG | 10451 |
rs184860910 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107794841 | GGCACAGAGAAAATA[A/G]TCCTCTCAAAGGATG | 10451 |
rs184868505 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107870011 | TAGTATTCCGTCATA[G/T]ATACAATTTCTTTAT | 10451 |
rs184907206 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107725174 | ACTCTTACAACAGTC[A/C]GTTGGGAGTCAGGTG | 10451 |
rs184921757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107934058 | CATTATCAGTGACCA[C/T]ACTCAAAAAGCTGTT | 10451 |
rs184930692 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107756981 | GTGATTTTAATATAC[C/T]TCTTAGTTTTATGCG | 10451 |
rs184957183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595518 | AGTGATATCAGATTA[A/G]GAAAATAAAATCACA | 10451 |
rs184968056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107641099 | TGTTGTTCTCTCTTT[C/T]CTTTTTCTGGGAAGG | 10451 |
rs184984173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107829527 | CTAACAGTATTTTAG[C/T]TTCTGTGTGGGCACT | 10451 |
rs185000014 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107668594 | ATTTGCAGTCATGGA[A/G]TACAATGAAATGTGT | 10451 |
rs185001875 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107791547 | GTCAGATGGCAGAGA[A/C]CCTGGCTGAATGTTA | 10451 |
rs185008983 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107647343 | ATATCAGAACATGTA[A/G]ATGTTTTATCCTGGG | 10451 |
rs185011972 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107953115 | TTTGGCAGCAGGAAC[A/G]GGAAACTTCACCGAA | 10451 |
rs185013944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107687067 | CTTGGCACTGCTGGA[A/G]GAATCCTGATAGCCC | 10451 |
rs185030202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721219 | TGGACAGCTATGGTG[A/G]GGGAGGAAAGTGAGG | 10451 |
rs185031042 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107738176 | CACTTGGACGAAGGG[G/T]GGGGAACATCACACA | 10451 |
rs185033706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707432 | AGTGATATATGTAAC[A/G]TGCTTAGAACACTGC | 10451 |
rs185042938 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107577211 | AGCTCTAAGAGGAAG[G/T]TACTAATATTATTTC | 10451 |
rs185047873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773686 | GGGACACCAGGGAGA[C/T]GGTGATCCATATTGG | 10451 |
rs185053824 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107752508 | GACAATATCAACAGA[A/G]TGAAAAGCCAACAGA | 10451 |
rs185055491 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107619553 | GGAGTGTGGTAGGAA[C/T]CATACACTGATTAAG | 10451 |
rs185069611 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107694619 | ATTCCACTTTTCCAC[A/C]ATCTAGTCAAGCTCT | 10451 |
rs185071742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597443 | ACCAGGAGCTTCAGA[A/G]GTCACAGAGATTATA | 10451 |
rs185078263 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107673762 | ACCAAACTGGAAACA[C/T]AGGCATTTAATAAAC | 10451 |
rs185080245 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107711429 | TTTTTTTAAGTCTAG[A/G]CAGATTGGCACAATG | 10451 |
rs185088324 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107665577 | TCAGTCTAGCAAGGG[A/C]GATAAGGCAGATACC | 10451 |
rs185093951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107725740 | CTACTCTCAAACTCC[C/T]GACCTCAGGTGATCT | 10451 |
rs185098019 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107684690 | ATCAGCATTGAAGCT[A/G]TGTTGAGCAAGATGG | 10451 |
rs185101271 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107811580 | TCTAGGTTATTAAAA[A/G]TTTTTCAAAAGTTAT | 10451 |
rs185106875 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107738889 | TACACTACTCAGACA[A/G]GCCGGAGACAGTAGC | 10451 |
rs185110690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107888238 | AAAGTGCAACATTCC[C/T]CACAAGTGACTTCAA | 10451 |
rs185112960 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107865141 | CTGCACACAGGTGGC[A/T]GGGGGCAGGGTAGGG | 10451 |
rs185117203 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107847836 | AGCTGAATTCTACCA[A/C/G]AGGTACAAAGAGGAG | 10451 |
rs185121244 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774594 | TCAAATGGTCAATAA[A/C]TCAAAAACAATCGAC | 10451 |
rs185128903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831381 | GAAAAGGCTATCAAA[A/G]TTGACAGGGAAATGC | 10451 |
rs185136440 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107647942 | TGACATCACAGCTTA[C/T]AGGGCTCTTTCTAAG | 10451 |
rs185139039 | snp | G/T | 0.0441095 | 0.141807 | intron-variant | VAV3 | GRCh38.p7 | 1:107812442 | TATTTATTATCATTT[G/T]TTAAGCTGATTTCCA | 10451 |
rs185145521 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107792902 | TAATGTATAATTCAA[G/T]CGTACATTATAATAA | 10451 |
rs185147289 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107687500 | GTTCATATAACTAAT[C/T]ACACATAGTTTGTAT | 10451 |
rs185173035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721559 | AGAGAAACACATCAG[A/G]CACTTCGGAAGGAAA | 10451 |
rs185184187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777618 | CATACCTGCAGGGTC[A/G]CCTCACCCACTGCAG | 10451 |
rs185207080 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107945682 | CAAAAATTGGCCAGG[C/T]GTGGTGGCGGGCACC | 10451 |
rs185210527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107907441 | TTTAAGATATATGTA[C/T]AACTGCTATCATTTA | 10451 |
rs185228056 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107869112 | GCAAATGTCTTATTG[C/G]TCCCAACTGAGTGAC | 10451 |
rs185244815 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107833897 | TAATCAAGCACTAGC[C/T]ATGGCAATGCTTACT | 10451 |
rs185275354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707984 | TCATATACTTTTTCA[C/T]ATTTACTTCTCAGAA | 10451 |
rs185276217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107954997 | ATTAGATGAGATAAT[G/T]CATGGAAAGCTTTAG | 10451 |
rs185276248 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107581199 | CAAACTGGATGCTTC[A/C/G]TTTAACGGCATAACT | 10451 |
rs185278118 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107727166 | TTTCAAACCCCTCTT[C/T]AAGTATGGATGAATT | 10451 |
rs185292958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107934949 | AGGAGAAGAGTTGGT[A/G]GTACATGAACCCATC | 10451 |
rs185293744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760501 | CTACAGAAGACTTGG[C/T]TGAAAAAATATTTTT | 10451 |
rs185295587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107623558 | CTGACAGTCCATTCC[C/T]TTACTCAAATGCTTT | 10451 |
rs185306258 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107648635 | TTAAAGATAGAAAAA[G/T]AACACAATTACACAA | 10451 |
rs185307352 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107913808 | TTTTTTAATTATTAT[C/T]ATTTTGAGGTGGAGT | 10451 |
rs185310582 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107926729 | ACTCAGCTGAAGTCC[A/G]CCCATGAAGGGAGTA | 10451 |
rs185314814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107601157 | TCTGGTCCAATTCTC[C/T]CTGTGCTCAGCCTGC | 10451 |
rs185324972 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107669612 | TTTCTTGCACAACAG[A/G]TTTTTTTGTTTTTCC | 10451 |
rs185339503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946775 | ATTGCTCAGTGTCTT[A/C]TAAAATTCTTCAGCT | 10451 |
rs185342795 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107688127 | CTCTGTACTTACAGT[C/T]CCATTTCATACACAG | 10451 |
rs185343296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107890563 | CTCAATAGTGAATTA[A/G]CAGTGTTTCACTTCC | 10451 |
rs185344755 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107908565 | AAAATAAATGTGTAC[C/T]GCATTTGTAACATGA | 10451 |
rs185351167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107862013 | CTGTCCTGACACCAC[C/T]GGTCCTCAGACACTA | 10451 |
rs185352051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107882027 | TGCAAACAGGATGGC[C/T]TCCCTTTTTATTTGA | 10451 |
rs185353964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107928708 | TACACAGTCAGAGGA[A/G]GCAAAAGAAAAAAAA | 10451 |
rs185359625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107849724 | ACAAAATTGACACAT[A/G]GGATCTAATTAAAGA | 10451 |
rs185364530 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107845122 | GGAACAGGCAGCAAT[C/T]TTTGCTCTTCTGCAG | 10451 |
rs185366431 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107891541 | TTAGTGTAGTCATTA[A/C]GAAAGGGCTCAGTTG | 10451 |
rs185367049 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107628865 | AATGAAGGTAACATG[A/T]TTTTCCATTTACCCT | 10451 |
rs185372717 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107826669 | CACTTAAGCTTCATG[A/G]TACTCAACAGACAGG | 10451 |
rs185373926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815109 | CTATACATAGATGCT[A/G]CAGTATCTGTCGTTC | 10451 |
rs185398667 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672710 | TTGAATAGAAAGAGG[A/G]AGTAAGCATAATAGA | 10451 |
rs185405877 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107709674 | GTGGGGATGGTTTCC[C/T]CCATCCTGTTCTCAT | 10451 |
rs185425570 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737956 | ACTTGGAACTAACCC[A/C]AATGTCCAACAATGA | 10451 |
rs185449641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107573551 | AGTAAATGATCGAAA[C/T]GGAGGAATAAAATAA | 10451 |
rs185450607 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107951166 | TCAATGTCTTTGCAC[A/G]TTCTTCATCTCACAT | 10451 |
rs185454806 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | VAV3 | GRCh38.p7 | 1:107922824 | GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCAGC | 10451 |
rs185456780 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107766094 | GCTAATCTACCTCCG[A/G]TGTTTACAGATGGGG | 10451 |
rs185469523 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107887734 | TACCACTACGATACC[C/T]CAACCCATACACCAA | 10451 |
rs185478142 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847182 | CGACTACTGGGTAAA[C/T]AACGAAATTAAGGCC | 10451 |
rs185496532 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107812235 | ATACTGCTGGCAGAG[G/T]TGACACTCTTGTGCA | 10451 |
rs185503101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654505 | GAAATGTAGGTGAAT[A/G]TTAACTTTAGGAATA | 10451 |
rs185505946 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107606566 | ATGCTGTATCCCCTG[G/T]GTCAACAGTCTAGCT | 10451 |
rs185533281 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693119 | TCAGAGAAGCTTGCA[C/T]AGTGGAGTTCATACC | 10451 |
rs185549890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107724621 | GACAATCCTACAGTA[C/T]AGGATGGGGGGTGGC | 10451 |
rs185573553 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107905138 | CAAGTCTATGGCATC[C/T]GGCAAGAATGAGAAC | 10451 |
rs185588367 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107944064 | CTGCCATAAGCTTCA[C/G]AGTCTCCCAAGGTCA | 10451 |
rs185593520 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782539 | TTCACTAACAGAAAA[A/T]TAACAAATATACAAA | 10451 |
rs185594414 | snp | A/G | 0.00755907 | 0.0610114 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965693 | CCCTCAAAGTGAGTG[A/G]GAGTGCGTGTGTGGA | 10451 |
rs185598762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107931635 | TATTAAAACACGTGA[C/T]TGAAATATTGTCATA | 10451 |
rs185599418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716367 | GTGTGGTGGCTCACG[C/T]CTGTAATCCCAGCAC | 10451 |
rs185600486 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107906152 | ATGAGCCCCCAAGGA[G/T]GAGATCTTCCAGCAT | 10451 |
rs185604995 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864027 | CAAAAATGAAGTATA[A/C]CCAGGTTTAAAAGCC | 10451 |
rs185606755 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107579535 | AAAGTGCTTTCTTTC[C/T]CTGCAATATGAAGTT | 10451 |
rs185607384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923627 | AAAAACCTTCTTTAC[A/G]TGGTGTCAGGAAAAA | 10451 |
rs185609737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888561 | CCTCCCAGGTTCATG[C/T]GATTCTCCTGCCTCA | 10451 |
rs185615698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107729573 | GAAGGGGCATGGGTA[C/T]GGAATCCCTGTTCTG | 10451 |
rs185616257 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | VAV3 | GRCh38.p7 | 1:107657035 | CTCAGCTCACTGCAG[C/T]CTCTGTCTCCCGGGT | 10451 |
rs185619676 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107744910 | CATCAAACTTGTACA[C/T]ATTTGCTCAAATGCT | 10451 |
rs185621473 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107865258 | GGCAGAGAAGCAGGG[A/G]GAAGGTCCCAGTTGA | 10451 |
rs185622865 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107829963 | TTATTTCATTTAAAG[A/G]ACTAAATTTAAGTGA | 10451 |
rs185632175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107763338 | GAGTCCCAGAGTATG[A/G]TCATTGGGCAAAACT | 10451 |
rs185640531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780736 | GGCCAGGCTGGTCTC[A/G]GACTCCTGGCCTCAA | 10451 |
rs185647262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107622648 | ATTTATGAACGATTG[A/G]AAATTCTCCCAAGTT | 10451 |
rs185712467 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107927984 | AGACCCAGTGCTATA[C/T]TGGCTTCAGAGCACA | 10451 |
rs185712491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787835 | CTCATTAGGCATTTC[C/T]GCACCACTATGGTCC | 10451 |
rs185720735 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | VAV3 | GRCh38.p7 | 1:107761217 | ACATGGTGAAACCCC[A/G]TCTCTACTGAAAATA | 10451 |
rs185748184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600015 | CCTCCTTCCAGAAGT[C/T]CAGGTTGCTAAAACA | 10451 |
rs185749118 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107900442 | CTTCAACTCTTAACA[A/G]GGAGAACATGAGAAG | 10451 |
rs185758503 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107633740 | ACTTTTACACTCTTG[A/G]GAGCCAGCTACCATA | 10451 |
rs185797498 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107580173 | TCCTCCACAGGATCA[C/G]GTCCAGTGCTAAGCA | 10451 |
rs185827155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107946157 | AATGGATTGGCATGA[A/G]GTAGAATACACATAG | 10451 |
rs185838148 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769391 | CAACTGGGCCTGTAA[C/T]GCTACATAGTGCTAC | 10451 |
rs185854625 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107733222 | CATCCACACCAAAAC[A/C]CCATTTGTAGGTCAC | 10451 |
rs185871149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107713035 | AGAAAGCTAGATTTC[C/T]ATTCACATTTTTATA | 10451 |
rs185873232 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767051 | ATGTTTTATTGACAG[G/T]ATAAAATAATGACTC | 10451 |
rs185877506 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107726577 | AAAAGCTAGCAGTTA[A/T]CAAGCTCTCTGGATC | 10451 |
rs185878397 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879657 | CTTCAGAGATATTTT[A/T]TGAGTCAGAAGGGCA | 10451 |
rs185881283 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107840081 | GTGAATTCTACCAAA[C/T]GTTCAAGGAAAATAT | 10451 |
rs185883595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107783017 | GCCAACAATCAACTA[A/G]AGTAAATCCATGTCA | 10451 |
rs185890407 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107821842 | GCTTGCAGAGTCCAA[A/T]TAACAAGAGCAAGGT | 10451 |
rs185900386 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107802933 | GTATCAGTTCTTTAA[A/G]TGTTTGGTAGAATTT | 10451 |
rs185904885 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107608917 | CCAATAAATTAAAAA[C/T]AGATTCAGTCTTTTT | 10451 |
rs185925710 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755153 | TGAGGGAAAGAAAAG[A/G]AAAAAAAAGTGGACT | 10451 |
rs185933760 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107771871 | TGAAAATGCTGCCAC[A/G]GATGGGCTGTCAGCC | 10451 |
rs185934620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654969 | ATAATAACAAATTGT[G/T]CCAAGAAGTTATAAA | 10451 |
rs185942694 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790486 | AGGGTTACAGAGGAA[A/T]GGCACACAGTGCCAG | 10451 |
rs185943268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943751 | GTCTCAAAACAAAAC[A/G]AAACAAAACAAAACT | 10451 |
rs185958320 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107877067 | CGGGAATCATTCTCA[C/G]AGGCTTAAATATTTC | 10451 |
rs185978643 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107905799 | TCTTCCTAATAAAAC[C/T]AAGCCATTTCTAAAA | 10451 |
rs185985282 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107841260 | TTCTTGTCCTCAACA[A/G]AGTTCATATTCTGGT | 10451 |
rs185992709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107718820 | TATACTACAAGACCA[C/T]AGTAACCAAAACAGC | 10451 |
rs185998476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804088 | GTTTTTACTTGCATA[A/G]AATATATTTTTCTAT | 10451 |
rs186000546 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107750637 | CACAAAAACCTCTGT[C/T]TGATGATTACATATA | 10451 |
rs186008951 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757186 | GTGTGTGTGTGTGTG[C/T]GTATGCAATTTGAAT | 10451 |
rs186021593 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107785048 | AATTTAAAAACCACA[A/C]AATAAAACAGCTTTT | 10451 |
rs186051472 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587438 | AACTGGGAATTTCTC[C/T]CCATTTAGATGAATT | 10451 |
rs186061797 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964550 | TCCCAAAGCAGAAGG[C/T]TGGGAAGCAGGGCAA | 10451 |
rs186071823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636702 | GTATAGTTTCTACTG[C/T]ATGTGTATCATTTTT | 10451 |
rs186082375 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107614921 | GGTTCCCAAACTTCT[A/T]AATGTTAGAATGTAT | 10451 |
rs186089258 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107922947 | ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAAAAA | 10451 |
rs186090428 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107659726 | TATTAAGGATATGCT[A/G]GTATTAAGGATATGC | 10451 |
rs186094550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897610 | GTTACACTATTTGGC[A/G]TCCTGCACCACCTCA | 10451 |
rs186098814 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107857976 | GATTTTATTTATGTA[A/G]CAAGTAATATATAGT | 10451 |
rs186101538 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107678404 | TAGAAACTTTACTAT[G/T]TATTATAGACAAAAG | 10451 |
rs186102568 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107705485 | TCTAAATAGATGTGT[A/G]GACAACATAATGGTC | 10451 |
rs186108179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107715888 | AGTGAATTTAAGTTG[C/T]ATCACATTTCAAATT | 10451 |
rs186120081 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728896 | GGATTCAGAATAGTT[C/T]TAAATTCATTATTCC | 10451 |
rs186120546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107823275 | ATAATGATTCTTCCA[C/T]TTTCTAAAATGAAGG | 10451 |
rs186126794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107733593 | GAACTACGTGACTCA[C/T]ACACAAGCTTCGGTA | 10451 |
rs186135022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107835878 | GGACCAGCAGACCTC[C/T]GGAATTCTGCAGGTT | 10451 |
rs186141192 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107860590 | TTTCTTTAAATGGCT[C/T]CTATTCTCTCCTTCG | 10451 |
rs186141625 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107767368 | TACCTTGGAGCACAC[A/G]TTGACTCCACAGCAT | 10451 |
rs186142940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107817227 | TGGTGGTTAACTCCT[A/C]AAGATGGTACTGGGG | 10451 |
rs186145281 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107843607 | CATCTGCTGAAGTAT[G/T]AGCAGGCGTATTTAA | 10451 |
rs186149277 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797347 | CACTTAAATATTTAT[A/T]GAGTATCTGCATATG | 10451 |
rs186157381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825599 | TCTCCTACATAAATA[C/T]TCTGTCAAACTGGTC | 10451 |
rs186182252 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774820 | ATTTAGAGTTAAGTA[C/T]ATTTACCCATAGAAA | 10451 |
rs186183404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107958874 | ATCTTTTCACATACA[A/G]ATACATATACACAAG | 10451 |
rs186204248 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920440 | CCAAACAAAAACTTA[C/T]GGGTGGTCCACCAAA | 10451 |
rs186207161 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107792201 | CTCACTTCACCATCA[A/C]ACTGCTAAAGCAAGT | 10451 |
rs186224530 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107637622 | GGGCAACAGAGCGAG[A/C]CTCCGTCTCAAAATA | 10451 |
rs186230821 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107679271 | AGCCACATGCAACTC[G/T]TTGTAATCAAGAGTC | 10451 |
rs186235057 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107708184 | CAGGATTGACATCAC[A/C]TTTAGTTGAGGAAGA | 10451 |
rs186243210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107735750 | AGTCCAAGACCAGAC[A/G]GATTCACAACCGACT | 10451 |
rs186262127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107852951 | AGTATTTTCATAGGA[A/G]AGAAAAGATTTGCCT | 10451 |
rs186277651 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107816598 | CTGCCTATAGGGGTT[C/T]ATTGGTATTTAGGCT | 10451 |
rs186308163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618478 | CTTATTAACAGAAGA[A/C]GACCGTAAGATTTTG | 10451 |
rs186309655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664221 | AAGTTCCAGAGTAAA[C/T]GTGCAAGATGTGCAG | 10451 |
rs186314110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587554 | TTGAGACCAGTTATG[C/T]ATGTATGTTTGTATG | 10451 |
rs186322604 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107682704 | GGTGAATACCACTTA[C/T]GATAGGAAAACAAAA | 10451 |
rs186324018 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107913436 | TCGCTCACAGCAACA[A/G]CAATAAAAACTTTAA | 10451 |
rs186329244 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702766 | CAGATCATGAAAACA[A/G]TAAAAATACTAAATA | 10451 |
rs186331982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107934378 | ACCCTTAGAACAGAG[C/T]AGAAGATATATTTTG | 10451 |
rs186344959 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896651 | ATCAAGATCAGCAGA[C/G]GTTGGAGGTGTGTGA | 10451 |
rs186354617 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107876811 | ATATGTAAGTTATAC[C/T]AAAATAAAGTTTAAA | 10451 |
rs186354733 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107857523 | CCATGACAATGAATG[A/G]TACAGGTTTAGGAAC | 10451 |
rs186365968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939196 | CGCCAATTTTAAATA[C/T]AAACCTTAGTTTTCC | 10451 |
rs186366051 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107660485 | AGAAAGACGGAAATA[C/G]GCACCAGGCCAAGGC | 10451 |
rs186367539 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107840956 | CTGGCAATCAAATAG[C/T]TTATACGGGAAGGCT | 10451 |
rs186368137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903037 | AAATAATTTTAAGGA[A/C]TAGGAAGGGCTTGAA | 10451 |
rs186372921 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822804 | GCAAAAGAGGTTCAT[A/T]CCTTCTATAATAATT | 10451 |
rs186398730 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722412 | CAAATGAGGCAAAAA[A/G]GCATACAGAAAGTAA | 10451 |
rs186406539 | snp | C/G | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689038 | TCATTACATTTCAGG[C/G]CCTGCAAATGCCTAA | 10451 |
rs186414662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107669844 | AAAAACTCCTTAGAG[A/G]AGAGAGTAACTACAT | 10451 |
rs186414847 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107700705 | CAGTCTATCACTGAT[G/T]GGCATTTGGGCTGAT | 10451 |
rs186416608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753919 | TGTCCAAGAAATATG[C/T]TATGGAATTCTAAAG | 10451 |
rs186419378 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107871153 | TGTCAAAAAATAATA[G/T]AGTAATTTCTAATAT | 10451 |
rs186425299 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107708451 | GTTCCCATTTCTTTT[C/G]CTTCACATAGAACTC | 10451 |
rs186429735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107722598 | TATGCTCCAAACAAT[G/T]TCCAATAAGAATACA | 10451 |
rs186430181 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107788899 | ATGGCAATTTTAATA[C/T]GTTCAATACCAAGAA | 10451 |
rs186431293 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736376 | AATCAGGCAGGAGAA[A/G]GAAATAAAGGGTATT | 10451 |
rs186432043 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107835261 | TGCCTTGCCATGGCC[C/T]CACATGAGTGCTTTC | 10451 |
rs186442523 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107754724 | TCCCTTCACTCTCCA[C/T]TTCCAGCCACTCTTA | 10451 |
rs186444743 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107576953 | CCAAGCATGCACATC[A/C]CAGCTTATTTTCAAA | 10451 |
rs186445565 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107796922 | TTTCTCCTCAAAATA[G/T]TAAATAGTTTAATTC | 10451 |
rs186446340 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107771404 | ACTACAGGTGCCCGC[C/T]GCCACGCCCAGCTAA | 10451 |
rs186485041 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107618581 | CTTATTGAATCCTTA[A/G]TATGTGCTAGACACT | 10451 |
rs186494298 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107665081 | AGTTTAAGTAGGAGA[C/G]GCCATGCTGTCTCTC | 10451 |
rs186503202 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107703896 | AGAAAATAAAGACAA[A/G]GAAGAGAGCCCAAGA | 10451 |
rs186504252 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107613879 | ATTTTTTATTTGAGA[C/T]GGAGTCTCGCTCTGT | 10451 |
rs186508077 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895596 | GGCTTCACAGTTACT[A/G]AACTATGAAGTTACT | 10451 |
rs186513648 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591557 | AATCAATGGACCAGA[C/G/T]GCTTCTATGTCTGAA | 10451 |
rs186515330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831818 | TTTTAGACATATTCT[C/T]ATGTAACCATAGTAA | 10451 |
rs186519917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107857312 | TCAGACTCCAAGCTT[C/T]TCAGCTTTGGCATTC | 10451 |
rs186522818 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107635948 | TCACTCATCTATAAA[C/T]TGAGGATAATAATAG | 10451 |
rs186524476 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107957355 | GACTTCAGTACCAGT[C/T]CTGCTCACGCCTAGT | 10451 |
rs186527540 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107909547 | TCCAATTGGTACAGA[C/T]TAATCACAAATTCCA | 10451 |
rs186528524 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107793880 | AAATCTGGGAGATAG[C/T]AAAGGAAGCAGATAG | 10451 |
rs186529522 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107759023 | GGCCTCTACTCAGGT[C/T]CCCAGCTTCCCTATA | 10451 |
rs186530047 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107929835 | TGTGGTACTTATACA[C/T]AACAGAGTACTACTC | 10451 |
rs186534882 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107892602 | GAATTTAGGCAAAAA[C/T]CAAAAAATTAGTTAC | 10451 |
rs186537187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107938741 | CTCAAAGGCTCCTAA[C/T]GTACTGGGCATTTAA | 10451 |
rs186553257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872199 | AATCACTATCCAAGC[A/G]CCTCCCCATGTCTTA | 10451 |
rs186558780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107854356 | TTAACAGACATAAGC[C/T]GACACCACCCTGGGC | 10451 |
rs186598375 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107956455 | CATACTAGAATTCTA[A/C]ACTGATAAGCCTTTG | 10451 |
rs186600016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107724546 | AGACATGAAAAGAAG[C/T]AAACCTAATAAAGTG | 10451 |
rs186606111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737703 | TAAAAAGTCAGGAAA[C/T]AACAGGTGCTGGACA | 10451 |
rs186610354 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107937701 | GTTAATCACAAGGTT[C/T]CTAGTGGCACCCTTA | 10451 |
rs186621118 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755843 | TAGAAATTCCAAGCA[C/T]GTTAATTACTGACCT | 10451 |
rs186628351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773432 | GTTACTGCAGTGTTA[C/T]AATCAGCATCTAATC | 10451 |
rs186651116 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107597274 | TTTCTTCTAAAAATC[C/T]CACTGCCATCAACTT | 10451 |
rs186694513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107643350 | ATATGTCTAAGCCAA[C/T]AGCACCAATGATATT | 10451 |
rs186698175 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107683094 | TCTCTGATGGAGGGT[A/G]GGTACCAGTTGTCTG | 10451 |
rs186715352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600833 | GCCCTTTTCAGTGAC[G/T]ATTCCTTTCATCTTC | 10451 |
rs186718626 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107718656 | TTTATAGATTCAATG[A/C]CATCCCCATCCAGCT | 10451 |
rs186726341 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107875725 | GATGGTTTAAAAAGG[C/T]CTTTTTGGCCTGTTG | 10451 |
rs186729636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107947940 | ACAACCTAGGAGTAA[C/T]AACTTATGGTGACGC | 10451 |
rs186730385 | snp | A/T | 0.0629771 | 0.165899 | intron-variant | VAV3 | GRCh38.p7 | 1:107848331 | AAAAAAAAAAAAAAA[A/T]TAGTGGCAAACTGAA | 10451 |
rs186746490 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107739698 | TATACAGACAGTTTA[C/T]AGACATATTTTGGCC | 10451 |
rs186765653 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107908809 | ATCACCCAACACCCC[C/T]GCCCCACTCAAACAC | 10451 |
rs186770393 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107871783 | TAAATCTCCTAAACC[A/C]CAAACAGAGGGAGAG | 10451 |
rs186771528 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107775637 | TAGAAATTAAATATT[C/T]CCCTTAAACAATCTG | 10451 |
rs186775645 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107889414 | AATGAAGAATGAATA[C/T]ATAATTTATTGTCCA | 10451 |
rs186779780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906634 | TCGCGCCACTGCACT[C/T]CAGCCTGGGTGACAA | 10451 |
rs186790268 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107744105 | AAGCTCAGGCAGGGG[A/C]TGCCGCTCCGGATGA | 10451 |
rs186794150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107867063 | AAAGTTTGTTTTCCT[C/T]ACTGCAGGACTTTTC | 10451 |
rs186796190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107849038 | AAGGACCTCTTCAAG[A/G]AGAACTACAAACCTC | 10451 |
rs186802616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107832801 | GTAAGCCATTGATTA[C/T]ATTGTACAAAATGTA | 10451 |
rs186806849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780346 | CTAAATTAACCTTAA[C/T]TATGTTTCAAAGATT | 10451 |
rs186809729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107813895 | ATTGCACTTAACATA[A/G]TGATCTCCAGAACCA | 10451 |
rs186820530 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794690 | ACCTTAGGAGCCCTG[A/G]AAGACTTCTTTTTCT | 10451 |
rs186827468 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107667353 | GAAAAAGCACTGAGC[A/T]GTGCAATGCTAACTA | 10451 |
rs186827469 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107713573 | ACATGTACTAGCAAT[C/T]AAAAGAAATGTACAT | 10451 |
rs186835123 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107726803 | CAGATGGAATAAAGC[C/G]TGCTAATTGAATTTT | 10451 |
rs186839802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807179 | CATTTCAAATCAGGG[C/T]ACTTCTCTAAGAAAG | 10451 |
rs186844746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707303 | CATAGGTAAGGACAG[A/G]AATCTGAAACTAGAC | 10451 |
rs186854718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686641 | TCCATCCACACAAAA[C/T]AGAGATTTTTAGTAC | 10451 |
rs186859752 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107740625 | GAAAAAAAAAATCAC[A/T]CTTCTACAAAAGGCC | 10451 |
rs186864745 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759292 | GAATCTATTAAGTAT[A/C]ATAAATCCATAAAAA | 10451 |
rs186873912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776605 | GAAGTTCCATAGCAT[C/T]TGAATCTGTCTTGGG | 10451 |
rs186923042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592280 | TCCTCATGATTAGAT[C/T]CCACTTATGCTTTTT | 10451 |
rs186940725 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107622760 | AGAGCGACTGTCACC[A/C]TGCCCAGTCACTTCC | 10451 |
rs186958392 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107731686 | AAGATAAAACAAGCA[A/G]TTTCAGAGGCAGTCC | 10451 |
rs186960972 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107929515 | ACTGGTAATAGTAAG[C/T]ACGCAGAAAAATACA | 10451 |
rs186971399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747031 | ACGACAGGCATGTGC[C/T]ACCACACCCGGCTAA | 10451 |
rs186986976 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107891950 | TATCCCTTTAAACTC[C/T]AGACTATAAAATGTA | 10451 |
rs186987154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781883 | TCAAGAATGAACAAA[C/T]ACTAATAAATTTATC | 10451 |
rs186990338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107597162 | GAAATGAAAATAAAC[A/G]AAAAATCACTTTTAA | 10451 |
rs187003779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107930177 | AATAACTAAAAGAGT[A/G]TAACTGGATTGTTTG | 10451 |
rs187012800 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107925060 | GAACAAAATATTGCT[A/G]CATGGGACAATGTGG | 10451 |
rs187013934 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107762319 | ACATGGAATGATATA[C/T]TATGAGGAGCTCCAA | 10451 |
rs187014454 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107949285 | ACAATTACTTATGAA[A/C]AATCTTTTTTCTTTT | 10451 |
rs187015828 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107904437 | AACAAAAATCACCAA[C/T]GACCTCTCAACTGCC | 10451 |
rs187022826 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107736873 | AAAGTTCATATGGAA[A/C]CAAAAAAGAGCCCGC | 10451 |
rs187024533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885745 | GTAAAACAACTGGCC[A/C]TACCTCACATAGCCA | 10451 |
rs187027623 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107863045 | GAAAAATAAAACATA[C/T]CTACTCGGTTGTAAA | 10451 |
rs187030853 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107846215 | GCTTCATAAGCAAAG[C/G]AGAAACAAAATCCTT | 10451 |
rs187038221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107604270 | ACCTGTAATGCAAAC[G/T]TAATATTCATTTAAA | 10451 |
rs187042174 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | VAV3 | GRCh38.p7 | 1:107954496 | GAATAGTGTGATAAA[G/T]GTGTATGAAATCATC | 10451 |
rs187045005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107828477 | TCAACATGCATCTCA[C/T]TTAAGCCAGTGAGAC | 10451 |
rs187052109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107585270 | CACCTATATGGCTAC[A/G]TGCTGTTCCAGGCCA | 10451 |
rs187054187 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107631089 | ATTTTTTAAATCATA[C/T]ACTAATTTGTCAAAA | 10451 |
rs187063161 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107671514 | ATACTTCAAATAAAG[C/T]AGAAGTTGAAATTTT | 10451 |
rs187065201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107712069 | TACACAACCTCTCTC[C/T]GATTTACAAATTTAA | 10451 |
rs187067416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107627473 | CCATATGTGCCAGTG[A/G]GACTCTTCACATTAA | 10451 |
rs187072309 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107652147 | TAAAGACCTTGCTGA[C/T]AAAACAGATTGCAGT | 10451 |
rs187082530 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107691031 | GAGTATCAGTAACTC[C/T]TAGAATCTGCTGAGT | 10451 |
rs187091050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709200 | AGTACTTGTAAGTCC[A/G]CCTCCCCACTGACCT | 10451 |
rs187152654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858501 | GGTACACAGCAGGAG[A/G]TGAGCAGTGCGTGAG | 10451 |
rs187152815 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107841922 | TGTATTATTAAAATT[A/G]ATTTTTCACTTTTTA | 10451 |
rs187160394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824188 | ATAAAAGTAATTGTA[A/G]TGTGGTGATGGGAAC | 10451 |
rs187166567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805095 | GCTTTTAAAATCCTT[C/T]CTTTGTCCTTGACCT | 10451 |
rs187207037 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107575923 | GCCCATGCACAAACC[A/G]AAGAACTGCAGAATT | 10451 |
rs187214100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751996 | AAAATTCCATTCTAA[A/T]ATTCTTATGGAATCT | 10451 |
rs187217083 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107767946 | AGTCTGGTAAATCAT[A/G]AGGAAGTAGGGTATT | 10451 |
rs187224370 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786357 | CTGATTAGAAGTGCA[A/G]GCTCAGAAGTCAGAT | 10451 |
rs187227139 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107944353 | TAAGTAAGTCTCAAA[A/G]AGAAGACCCAGAAGA | 10451 |
rs187234505 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655715 | CATTCATCTGACAGG[G/T]AATTAATAACTAGAA | 10451 |
rs187236167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906382 | ATAAAATAACAAATC[A/G]GGCTGGGCACGGTGG | 10451 |
rs187248466 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107945550 | CAGTCACGTCCAGGC[A/G]CGGTGGCTCATGCCT | 10451 |
rs187255952 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907225 | TGGTCATATACAAAG[G/T]TTTAGTCAAAAAGAT | 10451 |
rs187258924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107926340 | CCCATTGGCCAAACA[C/T]AGGACAAGTTGAACT | 10451 |
rs187260760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695014 | ATCTGCATTGACTTT[C/T]TGAAAATGAACATTA | 10451 |
rs187262514 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107587917 | TTTCAATTTAGAACA[C/T]GAGGTTATATGAGAC | 10451 |
rs187269908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726069 | ATTTTAATATTATGC[C/T]ATCAATATCCCTATC | 10451 |
rs187279248 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107889767 | TCAGGAAGCTGTATG[A/C]TCAGAAAGTGTCTTC | 10451 |
rs187280088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107611194 | GCATCATGTCAGTGC[C/T]TAAAAAGTTTGGACT | 10451 |
rs187282514 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107758035 | CAAAGTCCCCTCAAA[C/T]CCAACATTCCCCAAA | 10451 |
rs187289565 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107803398 | TACTGCTATAAACTT[C/T]CCTCTCAGTACTGCT | 10451 |
rs187293709 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107631567 | GTGCCATGTTGGTGT[A/G]CTGCACCCATTAACT | 10451 |
rs187304254 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107578791 | TCTCTCTGGGACTAT[G/T]TTATCCATAAAGAAA | 10451 |
rs187305462 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107675070 | GATCCAGCCCTGGCC[A/G]ATATCTTAAGTGAAG | 10451 |
rs187308233 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107655933 | AGAATGGCTTTTATC[A/G]AAAAGACAGAGGATA | 10451 |
rs187318970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624735 | TCATGGCAGCATGAG[A/G]TATTTTTAAAGAATG | 10451 |
rs187322771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959106 | GTCTCTACTAAAATA[C/T]AAAAATTAGCCAGGC | 10451 |
rs187326736 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582397 | AACCCTATTGTTTAC[A/T]GCTTATTGTATATAT | 10451 |
rs187329776 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658847 | GTAGATTCTGGATAT[C/T]ACACCTTTGTCAGAT | 10451 |
rs187342220 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107939981 | TGTATGGAACTGTCT[A/G]CTGCAGCTGTGGTTG | 10451 |
rs187352864 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107921046 | TCTACTGCAATTCAC[C/T]TTCACTCTGCTCCTT | 10451 |
rs187354555 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107699300 | GGCCTACAGGCCCCA[C/T]GCAAGTCTGAAATCC | 10451 |
rs187358025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902660 | TGTTTAAACCTTTAA[C/G]AAAATATTTATGAAG | 10451 |
rs187358584 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107855383 | CTGGATTCAAGCGAT[A/C]CTCCCACCTCAGCCT | 10451 |
rs187358850 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107882846 | TATGCTACATGTGGT[A/G]TCAGTTTAGGACTGC | 10451 |
rs187360734 | snp | A/G | 0.106987 | 0.205054 | intron-variant | VAV3 | GRCh38.p7 | 1:107728633 | TGTATATGTATATGT[A/G]TATGTATATGTATAT | 10451 |
rs187362721 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107904179 | CCAAATGACCCTTTG[A/G]TATCAATCAGAAAAG | 10451 |
rs187362746 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107838819 | AGATGGTGCTGGAGC[A/G]TATTAGCCTAGGTGA | 10451 |
rs187369622 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107820627 | TAATTGGAATATTTA[C/T]AACACAAAGAAATGA | 10451 |
rs187372773 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862547 | TTGTGTAGACAAGTA[A/T]ATTGACTATTAATAT | 10451 |
rs187383909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107639806 | AGGCATGGTGATACA[C/T]GCCTGTTGTTCCAAC | 10451 |
rs187385935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107861265 | TTCCAAGTAAACAAA[A/G]CTAAAAATACTTCAA | 10451 |
rs187394096 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107800615 | GCTGAGGTTTGGGGA[A/G]CAAATGATCCCACCA | 10451 |
rs187400435 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107663041 | AAATATGTTGAAGAA[C/T]TTATGTTTTAAGAAT | 10451 |
rs187405774 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | VAV3 | GRCh38.p7 | 1:107826279 | CATTTGCTCCATTAC[A/G]CTACTTGCTATGCAG | 10451 |
rs187421251 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107681724 | AGTGGCGCGATCTCG[A/G]CTCACTGCAAGTTCT | 10451 |
rs187422322 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107789853 | TATTTTTTATATTAA[A/C]TCTTCAAAATCCCAT | 10451 |
rs187424259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716851 | TGGTAGAATCCGGCT[A/G]TGAATCCGTCTGGTC | 10451 |
rs187427979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107701427 | AAGCTGCACACAGCA[A/G]TGGGGCCCTTGATCC | 10451 |
rs187432403 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107730999 | ATAATACCTTCTTAG[C/G]TACCTCACCAGACTC | 10451 |
rs187433332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107764360 | ACAATCTACCCACAC[C/T]GAAGTGGGTAGATTC | 10451 |
rs187444769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746236 | AAGAAGGAAATAAAA[C/T]AATGGAATATTCTGA | 10451 |
rs187502070 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107603940 | CTCCCAAGTAGTTGA[C/T]ACCACCGGTGTGGTT | 10451 |
rs187515152 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107583821 | ATATCGCGAAAATGG[A/C]CATACTGCCCAAGGT | 10451 |
rs187548813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107936069 | AACGTAGGACATTAT[C/T]ACAGTTCCTAGATTT | 10451 |
rs187555174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107955787 | TGAGAGATGAAGCAG[C/T]ACAAGACCATGAGCT | 10451 |
rs187561031 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107917095 | AGCTGGGTGCAGAAA[G/T]TCATCATGGTTTCTG | 10451 |
rs187566400 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107917799 | TTTCAAATTACATAC[C/T]GCATGGGCTTCCCTA | 10451 |
rs187579046 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948207 | TACCCTCACCTTTAC[A/G]GATTCCCCTAAACTA | 10451 |
rs187584424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107899972 | TCAACTATTCTTTCT[C/G]CATAAAATTCCTTTT | 10451 |
rs187588679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677467 | CAATGGCATATCCTT[C/T]TTTTTCTGAAATGGA | 10451 |
rs187596174 | snp | A/C | 0.000694444 | 0.0186214 | intron-variant | VAV3 | GRCh38.p7 | 1:107603039 | GTAAAAGTACTTGTC[A/C]TACTTACTTAATGCT | 10451 |
rs187600499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107878512 | TACAAAATGTCCTAA[A/G]TTCTGCATTTGTTTG | 10451 |
rs187602182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588986 | CATGGAAAGGCAATA[C/T]AATTCATTGAAAACA | 10451 |
rs187603504 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107859303 | CTTGAACTCCTGGGG[C/G]TCCAGTGATTCTCCA | 10451 |
rs187607202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656685 | ATGTGACTATATCAG[C/T]GTATCAAATTATTGC | 10451 |
rs187608478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612307 | TTGAATAAACTATCA[C/T]GATTTCATCCTTTTT | 10451 |
rs187610772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649088 | AAAAAAAGCAAGCAC[C/T]GTATTGGACAATCTG | 10451 |
rs187614851 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107842524 | GTGAACTTCTGTGGC[A/G]GTAGTTTCACTTTAA | 10451 |
rs187623903 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107666206 | AATCCAACCCACCAA[C/T]TGTCAAGAGTAAAAT | 10451 |
rs187626928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107715234 | CCGAGCACTCAAATT[C/T]GTTCTGAAGACAAGT | 10451 |
rs187629947 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107919290 | GCTCATCAATTTAAG[A/C]ATGTGATTACATTTA | 10451 |
rs187630275 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107880885 | GTTGTAGTGATGTTT[C/T]GGTGCTTGCTATGTG | 10451 |
rs187634573 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107696269 | ATTAGCATATCTATC[A/T]CCTCAAACATTTATC | 10451 |
rs187637028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107644740 | ACATTTCACCACCCA[A/G]ATATATATTAGGGAT | 10451 |
rs187639873 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107685592 | AGAAACCTTTCTACA[G/T]GAAGGGTGTGCAGTG | 10451 |
rs187642827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107743271 | CTGGTTGGGAAGAGG[A/T]AGGGAATAGCTAAAG | 10451 |
rs187645349 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107633769 | TATAGGAAGTCTAAG[A/T]ACCCTGCGATCACCA | 10451 |
rs187645624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612642 | TTTGCATACTGAGTA[A/C]TTTTATATTGTATCT | 10451 |
rs187653006 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107844838 | AACTCCCATCTCCCT[G/T]GGACAGAGCACCTGG | 10451 |
rs187656838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721081 | CAGATTTTAAGTTAA[C/T]GTCCAGAGTTCTAGG | 10451 |
rs187658461 | snp | A/G | 0.0490535 | 0.14873 | intron-variant | VAV3 | GRCh38.p7 | 1:107719660 | GTGTGGCAATTCCTC[A/G]AGGATCTAGAACTAG | 10451 |
rs187670432 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107807820 | TGTTAGATCTTTTTT[C/T]CTATTTTGCAGTGAA | 10451 |
rs187673384 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107752286 | AACTGGATATCCACA[C/T]GTAAAAGAATAAAGG | 10451 |
rs187673916 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107706151 | CTAAAATGATATGCT[C/T]CGAGACGTTACACGC | 10451 |
rs187680493 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107657202 | TCAAGTGATCCGCCC[A/G]TCTCGGCCTCCCAAA | 10451 |
rs187685091 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787669 | TATTCTAAGTAGATT[C/T]ACTTGCACCTTATTC | 10451 |
rs187687166 | snp | A/G/T | 0.00875309 | 0.0656392 | intron-variant | VAV3 | GRCh38.p7 | 1:107733612 | CAAGCTTCGGTAGCC[A/G/T]ATTCAATCAAGTGGA | 10451 |
rs187692372 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107781349 | TTACATATAGATGAC[A/G]ACAATGTATTACATT | 10451 |
rs187693774 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107751504 | ATTACGAGACGGTTC[A/G]GCAATTAATATTTTT | 10451 |
rs187704160 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107767816 | TTTAGCTTGCTTCTA[C/G]ATTTCTGGGCAAATA | 10451 |
rs187797383 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107813061 | CCAGGAGGCAGAGCT[G/T]GCAGTGAGCCGAGAT | 10451 |
rs187801102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921916 | TTACACTAGTTCATG[A/G]AGGATAACCTTAACC | 10451 |
rs187805770 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794583 | AAGGAGCAACTGTAG[C/T]TGAATTACATAGCTA | 10451 |
rs187820110 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593597 | AGCATACCTAAAGCT[A/C]TGAACCAAAGGTAAG | 10451 |
rs187821124 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107900470 | AAGTTTCTCTTCCAC[A/G]TGCAAAGTGAAATGT | 10451 |
rs187824345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107951281 | CTCTCTCACCCAGCT[A/G]CATGTACTTTTGCAC | 10451 |
rs187837790 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925855 | ATATATACCATATAT[A/G]TATATATAAACAGAT | 10451 |
rs187843335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893260 | ACTTTACTAGACTCA[A/G]TTTTAAACATTTGCT | 10451 |
rs187849599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588526 | TAGCACTTCCCACAT[A/G]TGAGATGCTATTCTC | 10451 |
rs187850688 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107960151 | AGTCTGTTCTCAATG[A/C]AGTAGCCAAAGTAAC | 10451 |
rs187855957 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107854982 | GCCTTTGCCATCTTC[C/T]AAAGCCAAAACCTCT | 10451 |
rs187867116 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107633324 | CCTCTAAGCATACAT[G/T]AGGCATGGTTCTAGG | 10451 |
rs187872598 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107820126 | ATACCCCAAAGAAAG[A/G]AAATCAGTATATCAA | 10451 |
rs187892904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594607 | TTTTTAAGAAAAAGT[C/T]CTGTAATTCCCTTCT | 10451 |
rs187897963 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107675528 | TGAATATGTTTAATA[A/C/G]AGATAAAATTTAAAA | 10451 |
rs187898785 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107639289 | TGTTAGATGTAATAC[A/C]TTTAGCATGATCCAT | 10451 |
rs187901238 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107616227 | ATAAAGAAAATATGG[A/T]ACATATACACCATGG | 10451 |
rs187915211 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107736940 | GGAGGCATCACGCTA[C/G]CTGACTTCAAGCTAT | 10451 |
rs187915878 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107661572 | CCAGGGACCATGAAA[C/T]TGTTCAATTGTTTAT | 10451 |
rs187930481 | snp | C/T | 1.65318e-05 | 0.002875 | intron-variant | VAV3 | GRCh38.p7 | 1:107772864 | ACAAAGGATATCATA[C/T]AAGGTCATTTTCTAT | 10451 |
rs187944902 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107734462 | CTGTATTCAGGAGAC[A/C]CATCTCACGTGCAGA | 10451 |
rs187965456 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107768316 | GGAAAAGCAAAAAAT[A/T]AATAAATAAGGCCAA | 10451 |
rs187979486 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107711730 | TTTTTTTGAAACAGA[A/G]TCTTGCTCTGTCGCC | 10451 |
rs187990551 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107726041 | AGACCAAAAAAAAAT[A/C/T]CTCTAATGAAAGATT | 10451 |
rs188007500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738901 | ACAAGCCGGAGACAG[C/T]AGCACAGTAACCACC | 10451 |
rs188013475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757682 | TTTGATTCTTTTAAC[C/T]GCATCCCTCCTTTCA | 10451 |
rs188023054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107774677 | ACTGTACAGTGTAGC[C/T]ATTACCTGCCCTCTC | 10451 |
rs188043498 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107810506 | TTTTTAAAATTGCTA[C/T]GAGACATGGAAGTTT | 10451 |
rs188047707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107837452 | GTATCATTAAAATGG[C/T]CATACTGTCCAAAGC | 10451 |
rs188052583 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107791056 | AGATGCTGAGTTCTA[C/T]ACATCGATAGTCTCA | 10451 |
rs188056969 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819167 | TTTTGTCTTTAACAA[A/C/G]ATTCTATCTTTTCCC | 10451 |
rs188065889 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941119 | AGCCTGGCATTTGGA[A/G]CATCACTCACTTCTT | 10451 |
rs188071047 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107692301 | ATACTTAGAAAGAGG[C/T]TTTGATTTCAAGTCT | 10451 |
rs188072648 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107946296 | GCTTGACCAGTATCA[C/T]GAGGTAGCTACTTTT | 10451 |
rs188077389 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107709409 | TGGAAGAAGTAAAGG[A/G]AAGATAAGAGACATT | 10451 |
rs188083414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907816 | TCAGTCTCTAGACTA[C/T]AAGAAATAAATTTCT | 10451 |
rs188087461 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107928358 | CCAGCCACAGACAAA[C/T]ATCCACAAGCACCAA | 10451 |
rs188087951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107935382 | TCAAAGAAGTAAATA[C/T]ATAATTCTCCAGGAA | 10451 |
rs188091969 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573033 | AAGTAAAGGGAAGCA[C/T]GAACCAATGTGTTTG | 10451 |
rs188092776 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107898605 | GTCCCTGCAGGGTAA[C/T]AGGAAGCATTCAGCA | 10451 |
rs188093732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107890844 | ATACAACTTCCTGAA[C/T]AGACTGTGCTAGATC | 10451 |
rs188097172 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107682497 | TAAACCAGAACCCCT[A/G]TTTTTTTAATGGCTT | 10451 |
rs188105936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107870267 | AGCAGCGTAGAAGTG[C/T]TCCCTGATCACTGCA | 10451 |
rs188112767 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107621700 | GCTTGTCATCCCTTT[C/T]ATGAGTATTACAAAT | 10451 |
rs188114499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107833650 | TCTTTTTCAAGGGAT[C/G]AGTTCTGAATATTCA | 10451 |
rs188119736 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107872728 | TGCACTATGGTACAG[G/T]AGTGGACAATCAGCT | 10451 |
rs188124203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107834395 | CTAAGGCAGGAATTT[A/T]AAAAATGTTCCATTG | 10451 |
rs188128836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794912 | TGAGTGTGGGGTGTG[C/T]CACTGATGCACTAGG | 10451 |
rs188132283 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107615315 | ACGTGAATTAACACA[G/T]GAAAGGAAAAGCAAA | 10451 |
rs188134274 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107816008 | GGCAATACACTTTGC[A/T]CTTCTATGGGAATCC | 10451 |
rs188140346 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107838127 | AGAATATATTCGCAA[A/T]CTATGCATCCGACAA | 10451 |
rs188149060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667054 | CACTTAAAATCAAAA[C/T]AAGACAACAGCATGG | 10451 |
rs188150415 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107706841 | AAACAGAAGTACATC[C/T]CCTTCAGGCAGAAAC | 10451 |
rs188161704 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107798915 | ATGCAAAGATGCTTT[C/T]AGAGTTGTACAACAA | 10451 |
rs188179696 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107733842 | AACCAGGAGGACGTC[C/T]CCAACCTAACAAGGC | 10451 |
rs188184084 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107723763 | ATGTCTTCCATACTT[C/G]CATATTTCTCTTGGT | 10451 |
rs188206179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755677 | CAAAGCTGCATCACA[A/G]AGGCAATTTTAAAAT | 10451 |
rs188222721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790912 | AGGCTGGTCTCAAAC[C/T]CCTGACCTCATGATC | 10451 |
rs188251439 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107728343 | AGTCTCAGTTCCACT[C/G]TTTACTACTCCTGTG | 10451 |
rs188252973 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107742649 | TTTCCATTCCCAGAT[C/T]CACGAGGCTTTCTTT | 10451 |
rs188265533 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761031 | AGTATCTTCAATTTA[A/T]AAAAACAAATCTTGT | 10451 |
rs188271640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107779218 | AGTCACCTGTGAATT[A/G]AGAACAATGTTTAGC | 10451 |
rs188290326 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599812 | TGTGTTTCACAGATA[G/T]AAGAGTAAACTAATA | 10451 |
rs188304184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579087 | GGGTGCTAGCCCTCT[C/T]TCTTATCTAACTCTA | 10451 |
rs188310749 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107646635 | TTGTTGTACAGCTAA[C/G]TATGCCCTTAATATA | 10451 |
rs188317817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950323 | TGCTACTGTTACTTC[C/T]AGTAACAATAATAAT | 10451 |
rs188324588 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107622368 | CCAGGATGCTAGAGC[C/T]AAAACCTCATTTTTA | 10451 |
rs188334269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923123 | TCCATCCCTTCCTGT[C/T]TCTAGCATCTACCAA | 10451 |
rs188342581 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107933285 | GGTGGTTTTTTTGTG[G/T]TTTTTTTTTTCCAGT | 10451 |
rs188348500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107910293 | TCTGCCATGGGTCAT[C/T]AGTTATTAAAACAAA | 10451 |
rs188350024 | snp | C/T | 0.110872 | 0.20771 | intron-variant | VAV3 | GRCh38.p7 | 1:107952794 | AATACCCAGCATCTA[C/T]TACAAAGTCCAACAT | 10451 |
rs188353409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107955505 | AGCCTGGAAGGGAGA[C/T]GGATAAGGAAAAAAA | 10451 |
rs188360924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107573727 | AGCAGTTCTTATAGA[C/T]ATTTTGCAATACACA | 10451 |
rs188379590 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107617069 | ATCTGTGTTTTATAT[C/T]TTCAGAAAATTCCAT | 10451 |
rs188381745 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107650911 | AACAATGATAGACTG[G/T]ATTAAGAAAATGTGG | 10451 |
rs188382378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107849384 | ACCAAAACAGATATA[C/T]TGACCAATGGAACAG | 10451 |
rs188386250 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107915284 | AATGAGATGCAAAAG[A/C]CTCAATCAGTAGTGG | 10451 |
rs188390665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599042 | TTTGGCTAGAAACCA[C/T]AGAATTATCATACTG | 10451 |
rs188394185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107845289 | CACAAAAACCCCATT[C/T]AAAGATCACCAACAT | 10451 |
rs188400566 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107878038 | TTTCCAGTTTATTTA[C/T]TTTATTTTTTTGAAT | 10451 |
rs188404999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814489 | ACATACTTTTTAATG[A/G]GATTACTTACTGTTG | 10451 |
rs188408232 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107809660 | TATTCAAACAACATT[C/G]CAAAACAATAGCATA | 10451 |
rs188410396 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689939 | GACCCATATACACCA[G/T]AATATCCCTATTCCC | 10451 |
rs188414463 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723499 | GCCAACATACACCTG[A/G]ATTCTCCATCTGGGC | 10451 |
rs188419490 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107645980 | CTTAAAAATCTCTAC[A/G]TAACTTCTCTCCATT | 10451 |
rs188431106 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107685835 | ATACTCCCCTCCCCA[A/G]TCTATATTCTCAAAA | 10451 |
rs188454134 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107720157 | CAGCACATGTATACA[C/G/T]ATGTAACAAACCTGC | 10451 |
rs188454575 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107630071 | CCATTGTAACATCTC[C/G]ATAAGTTTTCTAGAT | 10451 |
rs188469552 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107607401 | AGTATGTGTATATGG[A/G]ACCCAGCTGTCACAG | 10451 |
rs188470688 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781647 | GACTAGATGAGCTAA[G/T]TTACTGACCCCAAAA | 10451 |
rs188474033 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107673517 | CATCATTTCCTGATG[C/T]TCACATATCTAAAGT | 10451 |
rs188482103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654928 | AATGTAAACTGTAGG[C/T]TATAAAGAAAAATAA | 10451 |
rs188484226 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693958 | TATGGGTCTGTAAGT[A/C]AGCAACCCTAGAACC | 10451 |
rs188503426 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107777995 | TCCTTGTTTGCATCA[C/T]GGTACTATGTCCTTT | 10451 |
rs188506585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710908 | ACTAAATAAACTAGA[C/T]ATTAAGGGATAGTTT | 10451 |
rs188514697 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107725568 | TGCCCAGTCTGGAGT[A/G]CAGTGACACAATCTT | 10451 |
rs188551925 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107811038 | GATAGTTCAACTTTC[A/G]GAAGTCCTTTCTCTA | 10451 |
rs188560413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107791136 | CCTCCTAACTCTGGG[C/T]ATGTTTGCTGTGATT | 10451 |
rs188572876 | snp | A/G | 0.000135163 | 0.00821967 | intron-variant | VAV3 | GRCh38.p7 | 1:107574250 | AGTTCGTTAACAACC[A/G]TAACAACCTAATCAG | 10451 |
rs188585629 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107928884 | GTAGAGAAAGATATC[A/G]ATATCCAAGTATAAT | 10451 |
rs188591343 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947022 | CAAGGGAACCCAGAG[A/G]GAAAAGAGCCTGCCC | 10451 |
rs188595677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107908567 | AATAAATGTGTACTG[C/T]ATTTGTAACATGAGA | 10451 |
rs188618711 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107930505 | ATTGGTAATCAAAGG[A/C]AAATAATTACCTAAC | 10451 |
rs188625233 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107893567 | TGTCTTACATGGATG[A/G]CAGCAGGCAAAAAAA | 10451 |
rs188646926 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107598138 | GCAGGCGGATCACCT[A/G]AGGCCAGGAGTTTGA | 10451 |
rs188647199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888834 | CTAAATTACATTCTA[G/T]TTTCTGTCTATATTT | 10451 |
rs188653926 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824439 | GGAGGTTCAAATGGA[A/T]AATGACATGTACATT | 10451 |
rs188663992 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107848464 | ACATAAACAGAACCA[A/G]TGACAAAACAACCAA | 10451 |
rs188672620 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107626637 | GCCAAGATGAACAGC[G/T]GGACACTGGGAAAAC | 10451 |
rs188675904 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107675680 | CCTTTAAGGATGGCA[C/T]CTTTCTTCAATTCTG | 10451 |
rs188679745 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107670704 | CACAAATGTTGACTT[A/G]GTCCCAAATAGGGAT | 10451 |
rs188679905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595057 | ACTTCCATTTTTGAA[A/T]GAGCAAAAATTATGC | 10451 |
rs188682276 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107827235 | AACTACTTACTACTA[C/T]TAAGGAATGGAAAGG | 10451 |
rs188688544 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107708958 | CACACACATACCCCC[A/C]CACACACCCTATCCT | 10451 |
rs188694109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613078 | GAGCTATTCAACAGT[C/T]ACCAGAAGTGGAAAC | 10451 |
rs188704057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107580180 | CAGGATCAGGTCCAG[G/T]GCTAAGCAACTGAAG | 10451 |
rs188709499 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107634823 | CAAAGGATATGAACA[G/T]ACACTTCTCAAAAGA | 10451 |
rs188709723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107714062 | AGATGTTCACTTATA[C/T]GCATTATTTTTCCAT | 10451 |
rs188722247 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107741404 | GCTCCCTGAAGGGGT[C/G]GTGAGGCAAGGGGTG | 10451 |
rs188726654 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657850 | TTCACTGGTGTTGTT[A/T]AAAATGTTATGTTCA | 10451 |
rs188734929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600953 | AGTCCCATAGTAACT[A/G]TAACACTGTGGAGCA | 10451 |
rs188735116 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107698372 | GCCACGAAATCACAA[G/T]GGGAAGCAAACAATA | 10451 |
rs188736466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107776698 | GAGGAGTAACGATCA[C/T]GCATATATTTATTTG | 10451 |
rs188741049 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107675950 | TTCCTATTTTAGGTT[C/T]ACTTCTCCACATCAA | 10451 |
rs188742968 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107714167 | ATTGACCTTTTGAGA[C/T]CAATACTATGATGGA | 10451 |
rs188746179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107764739 | TAACGTATCTCACTC[A/G]TCCTGCACTTCTTAC | 10451 |
rs188759397 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107727335 | TTCTGTTTTTAAGAT[G/T]ATGAATATGATCTCC | 10451 |
rs188763429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107742402 | GGCAAACAGATCTAA[C/T]GGCAACCCCATATTC | 10451 |
rs188770345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860345 | TAGTAGATATATGAG[C/T]GGTGATTGTAGTAGT | 10451 |
rs188772076 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880554 | TAATCCCAACACTTC[A/C]GGAGGCCGAGGTGGG | 10451 |
rs188785668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107843306 | GGATGATAAGAGTAC[C/T]TACTAATAAAATTGT | 10451 |
rs188791609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825411 | AATCTATATGATTAC[A/C]CTTTACCAAATATTT | 10451 |
rs188799837 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107806566 | AGAACATACGTTGGA[A/G]TATTTGGTACAATTT | 10451 |
rs188872663 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940695 | CATGGATAAACCTTC[A/G]GGACATTAAACTAAA | 10451 |
rs188875198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107904252 | TGTTAAAGAATGCCA[C/T]GTTACTGCTAGATGC | 10451 |
rs188904695 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107862790 | ATTAGTGAGCATATA[C/T]GTGCCATAGCCTTGG | 10451 |
rs188910230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620733 | CGTTGGGGAGTGCAA[C/T]GTCACAAAGCAGAGA | 10451 |
rs188921142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107577742 | TGAAAGAAACTGGAT[C/T]GCTAAAGATTTCCTG | 10451 |
rs188921641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107827910 | TGGTCAATTCCTATT[C/T]TAGACCAACTAGAGG | 10451 |
rs188925078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107866587 | TTTGGGAGGGAGAGG[C/T]GGGTGGATCACCTGA | 10451 |
rs188932544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769847 | CATCATCCAATCCGG[C/T]TGGTTCTATGTTTAA | 10451 |
rs188937435 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107700914 | TAATTTACATTCCCA[A/C]CAACAGTATAAAAGC | 10451 |
rs188938479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788456 | GAAATTCCAGCAGAG[C/T]ACAAAATTCACATGA | 10451 |
rs188941830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805331 | ATTCTATATCTCATA[C/T]GTGACCTGTCATTCC | 10451 |
rs188944123 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832588 | AAACTCCAAATTACT[A/T]AAGCTTATTTTTTAA | 10451 |
rs188947391 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628752 | ATATATAGAACTAAA[A/G]TAGGGGACCACAAGT | 10451 |
rs188949777 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107586000 | CATTGAACTAACTCA[C/G]AAGTGATGAACCAGC | 10451 |
rs188961148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672491 | GTTTAATAAGTCAGA[A/G]GAGGGAAAATTTTCT | 10451 |
rs188964424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107629261 | AGAAACCATAGATGA[C/T]ATGGCTTAATTTTAC | 10451 |
rs188967401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107730139 | GTCAAACACATGGTT[C/T]AGATAACCACTTCAA | 10451 |
rs188977095 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107702545 | AGACAAAATGACTTA[C/T]GTAAGGACAGAGTAC | 10451 |
rs188977562 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107697048 | AAAATAGTACCTACT[A/T]TACCACACTCACATC | 10451 |
rs188978824 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107607018 | GGTGTGCAGTGGTGT[A/G]ATCTCGGCTGCCTGC | 10451 |
rs188984377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963578 | CAGATGACTGTGTGT[A/G]CTCTAACTTTAAATA | 10451 |
rs188987951 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107726922 | TGTAAATCCACACAA[A/G]CACATGTATACACAT | 10451 |
rs189000349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786272 | ATTCTATACTTACTA[C/T]TTTTTGAATCTTCAA | 10451 |
rs189001902 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107731899 | GGGAAAAAACAACTA[C/T]GACAAATCAGTTTTT | 10451 |
rs189004669 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107941658 | TTAAATTTTCATACA[C/T]TGATCCCATTTTCTT | 10451 |
rs189005379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760305 | ATAGCTTTGTGGGCT[A/G]TAACAAGAATCACTT | 10451 |
rs189014221 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107904831 | GAACTTATTAATTAC[A/G]TGTAATTATCATTAT | 10451 |
rs189016646 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107922674 | AGAGCACAATTTGGC[C/T]GGGCGCGGTGGCTCA | 10451 |
rs189020803 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107876359 | AGAAAAGGAAGTGAA[A/G]ACAGAATATAGACTC | 10451 |
rs189020907 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107765447 | ACTGGCTTGATGACT[A/G]TTAATGTTATTTGAG | 10451 |
rs189024850 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107887637 | AAAAATCTTTTACAA[A/C/T]GCATGCGTCTTAATT | 10451 |
rs189026539 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107857365 | GCTTGCAGACAGCCT[A/G]TTGTGGGACCTTGTG | 10451 |
rs189030610 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840492 | TTCCCTCTCAGCCAC[A/T]AATGCTCCATTCCAG | 10451 |
rs189043226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107821882 | AGAAAGTGATTTATT[C/T]CAAAGCTATCTTAGG | 10451 |
rs189135886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664377 | AGGCCCCAGTGTGTG[C/T]TGTTCCTCGCCACTG | 10451 |
rs189136935 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107879700 | TGTTTCATAACCATA[A/C]CTATTTTTGACAAAA | 10451 |
rs189154702 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107682975 | AAAACAACTGAACGT[A/T]TTCTGCAGACAAATA | 10451 |
rs189165039 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107718254 | TTCAATTAGGAAAAG[A/G]GGAAATCAGTTTGTC | 10451 |
rs189165688 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV3 | GRCh38.p7 | 1:107921755 | AATCTTTAGTTCTAA[A/G]GTGAAATTATCTACT | 10451 |
rs189179666 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107773494 | CATTCAGAGGAAACC[C/G]ACCAGTCCCCCATCA | 10451 |
rs189179847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805866 | CTTTCCAGCATTAGA[C/T]GGAACCTTAAACCCA | 10451 |
rs189180765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107883812 | TAAGAGGAAGCACTG[C/T]ACCCCTCTCCCTTGG | 10451 |
rs189181518 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107732949 | AGCCTAACTGGGAGA[C/T]ATCTCCTAGTAGGGG | 10451 |
rs189183370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747761 | TATGCAGCCAGTTCA[C/T]GGCAGTGATAATAGA | 10451 |
rs189185210 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107834238 | AATAAATGCATGATA[C/T]ACCCGTAAATTATTC | 10451 |
rs189188500 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107845669 | CACAAGTATCAACAG[C/T]CAAATAGATCAAACA | 10451 |
rs189189890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815189 | TCTCTTAGGAAGAAA[A/G]TCCCACATCCCACTC | 10451 |
rs189191481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107766119 | ATGGGGACACAGAGG[C/T]TCAGAGAGTTAAAAT | 10451 |
rs189200647 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107795366 | AAACTCTTACAGGAC[G/T]ATCAAACAATGAAAT | 10451 |
rs189202163 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107782607 | TGTATCCCAAAGTGA[A/G]TGAGAACTGGCACTC | 10451 |
rs189203358 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107613761 | TGCCTAGGACTTTAT[A/G]TTAAAAATCCTTTGA | 10451 |
rs189210404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107680340 | AATCTGAAAATGACT[A/G]TGATTATGTAGCTTC | 10451 |
rs189221572 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107658184 | TAACAGGCCTATGAG[C/T]GAGAACATGCGGTGT | 10451 |
rs189222848 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107606028 | AGCCTGTTGAATTAC[C/T]GTAGTCCTGGGACTT | 10451 |
rs189227231 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107653232 | CCATCATTTCGATGT[A/G]CTGATTTTTTTTTTT | 10451 |
rs189244196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107716461 | GCTGTTCAATTTTGT[C/T]AAAGGCCTTTCCTAC | 10451 |
rs189245622 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107938244 | CAGGCTAACCAACTT[C/T]GAGAAATGTCCCCAC | 10451 |
rs189255059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699038 | TTCTGCTCCTGGCCC[C/T]TCCCAAAACTCACAT | 10451 |
rs189256874 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107745804 | TGGCAAGCATTTCAA[A/C]ACTCTTAAAAATATC | 10451 |
rs189257647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107957306 | CTCTATCCCTCTATT[C/T]ACCTCCTTTCTCTGG | 10451 |
rs189266293 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107918999 | GGCACGAGCCACCCC[C/G]CTGGACCAAGGCATA | 10451 |
rs189270947 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107717543 | TTCCATGTAGTTGTG[C/T]GGTTTTGAGTGAGTT | 10451 |
rs189274395 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107880701 | CTGGGGAGGCTGAGG[A/C]ATGATAATCCCTTGA | 10451 |
rs189276606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902187 | AAGATGAATTCTAAC[C/T]TTCCAAGCTAAAGGA | 10451 |
rs189291725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107747604 | ATCACCTATTGTTCA[A/G]TATCACATAGCTGTA | 10451 |
rs189294848 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860718 | AAAGAAAGAACTGAG[C/G]AGACGACGTTTATTT | 10451 |
rs189302704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107754116 | CAATGTAAAGTTTAC[A/G]GGCAGTTATTAGCTG | 10451 |
rs189310285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107782170 | AATAGCAATAGCAGT[A/G]CTACGGTTATGTCTT | 10451 |
rs189318552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107789489 | ATCTAACAGAAGTTA[C/T]GACTGCCTACCAGAC | 10451 |
rs189324691 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965218 | GGTCTCGCTGCGGTC[A/C]GCAAGTCCCCAGACG | 10451 |
rs189394021 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107895133 | AGAGGAAAAAAAAAA[C/G]AGCTATGGGAAGCAG | 10451 |
rs189394527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107687274 | TCTTTATATCACACT[C/T]TTGATATCCTATATG | 10451 |
rs189398660 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635971 | AATAATAGTAATTCA[A/T]TTTATAGAATTTTCA | 10451 |
rs189403327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910764 | GCAGGCAAATCACCC[A/G]ATGTCAGGAGTTTGA | 10451 |
rs189406487 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677779 | TGTATATTTTCCATC[G/T]AAAAGCACCCCCATG | 10451 |
rs189407354 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107932056 | GGCAACAAGAGCCAG[C/G]CTGGCACACTGCACT | 10451 |
rs189407952 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107856349 | AGTTGGGAGCTATTG[A/G]GTAGAGGATATTGCA | 10451 |
rs189411598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894205 | CCAAATAATGGTATA[C/T]GTTTATTAATTTAAA | 10451 |
rs189416983 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659228 | TATATTTTTAAGACC[A/T]GGAGGCTAAGCATTT | 10451 |
rs189417105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707434 | TGATATATGTAACGT[C/G]CTTAGAACACTGCCT | 10451 |
rs189418249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821458 | AAGCCTCTCTAAAAA[C/T]GTGTCATTTACACTG | 10451 |
rs189423092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721493 | AAAACAGGGTAGGCA[C/T]AAGGGCCACAAGGCT | 10451 |
rs189425197 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107735020 | GTCTCTCAGACTACA[G/T]TGTGATCAAAGTGGA | 10451 |
rs189427721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107830264 | GTGGAGGGCAGTGAT[A/G]CAATCATAGCCCACT | 10451 |
rs189429646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107856029 | GAAGCAACAGAAGCA[C/T]AGCTGGGCATGTTCT | 10451 |
rs189431744 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107874095 | TCTCAATAGCATTAG[A/T]TTTTTCCTCCTTATT | 10451 |
rs189432819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107752850 | TTGTGCATTGGTAGT[A/G]GGAAAGTTAAGTGGG | 10451 |
rs189435798 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107860176 | CCCAGGCGAGAATGC[A/G]GTGGCATGATCTCGA | 10451 |
rs189437403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812381 | CCTATTTGTGTCACA[C/T]GTGTGCCCGTTTTCA | 10451 |
rs189441382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107769393 | ACTGGGCCTGTAACG[C/T]TACATAGTGCTACTA | 10451 |
rs189443284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107792275 | AACTGTATTATTACA[A/G]GAAAACTTTTCAGTG | 10451 |
rs189443413 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107839439 | AGTAACTTATGAGTC[A/G]AAAAATTCACAAATG | 10451 |
rs189447071 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796252 | GTCACATGGTCTCTG[A/G]GCCCCAGGCTCTCAT | 10451 |
rs189449566 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825028 | GTGGTCCAAGTCTGT[C/G]TTAACATTTTGTAAA | 10451 |
rs189454209 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787903 | TGAAGACCCCAAACA[A/G]AGCATCTTTTCCTCC | 10451 |
rs189467410 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107595788 | AATTCTTAAAGTAGT[A/C]ATTGAAATAGACCAT | 10451 |
rs189479279 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107641209 | TGGTTAGAGACAAAC[A/G]TTCAATCTTTGGGCA | 10451 |
rs189483648 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107681860 | AGAGATGGGGTTTCA[C/T]CGTGTTAGCCAGGAT | 10451 |
rs189501296 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591505 | ATGGCTTCAAATATG[A/T]TCTGTTCAGTACATG | 10451 |
rs189514975 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107717366 | TCCTGCTTTCTCTTG[A/T]GAGCATTTAGTGCTA | 10451 |
rs189515984 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635673 | TGCCACAAATTTGAT[C/G]GTGACAGTGAAAGAA | 10451 |
rs189521973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676709 | TAGGAACAGACTGAT[A/T]ACTTCATTTAAACAT | 10451 |
rs189523250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619816 | ATGCAGTGTACAGGA[A/G]AATAAGTGACATTTT | 10451 |
rs189535662 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107644396 | CTCCTTTTTATTGAG[C/T]ATACCTAGGGCAAGG | 10451 |
rs189537789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597585 | AATACAAGTAGCTTG[C/G]CTTAAACTGAAGAAC | 10451 |
rs189544600 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738372 | AAAAAGAAAAGAAAA[G/T]AAAATATATTGTCTT | 10451 |
rs189548707 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107665935 | CTGTAAATGCAACTG[C/T]TGAAGGAAGGTAGAA | 10451 |
rs189561381 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107705533 | TAATTTTATAGAAAG[C/T]TTTAAAATAAAGCAT | 10451 |
rs189563021 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107773736 | CTGAGGGGTTTAGGC[A/G]GCAATCTGGCCAGAG | 10451 |
rs189567617 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107684773 | TTTGCTCTAGATTTG[C/T]TGGTAGCCAAGGCAC | 10451 |
rs189590560 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107770841 | TCCTTTCTAATACAA[C/T]ACATAATTGAAAGAC | 10451 |
rs189616862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107596559 | GGCCATTAATAATAT[A/G]AGTTACCCCCTATTG | 10451 |
rs189620231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943794 | CAGTTTGAAGTCGTG[A/G]CCTAGAGCCTTGACT | 10451 |
rs189628261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107642051 | CATGCATTAAATCTA[A/T]CAAACTGTAATTCGG | 10451 |
rs189638420 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107618111 | ATGAGAATCTAATGC[A/C]GCCACTGATTTGACA | 10451 |
rs189646968 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107663885 | ATCACTTTATAAGAC[A/G]TGTCTGTGTTCTATG | 10451 |
rs189654759 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107937812 | TGACTGCATTAATAT[C/G]TATACACTATAGGTA | 10451 |
rs189658926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900813 | AACAGACATATCTTA[C/T]ACAAAACTATTTGTG | 10451 |
rs189663066 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107871659 | CTTCTAGAGAAGCCC[A/G]AATAGATGCTCTTCA | 10451 |
rs189665256 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107911398 | AAATTCAAAATGATA[A/C/G]TAGGTCACCCATGTA | 10451 |
rs189671410 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107875474 | CAAGCCATGGAGAAC[C/T]GTAGCACACAACAGC | 10451 |
rs189682430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808029 | TTCATAAACCTGACC[A/G]ATGATGATTGATTTT | 10451 |
rs189703354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802172 | CACTGTTGGCTTACA[G/T]AAATGGTACTGATTT | 10451 |
rs189727435 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107617961 | CCCAGGGATGTGGGG[A/T]GAGGTGAGGTGGGTG | 10451 |
rs189731455 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107948610 | ACACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC | 10451 |
rs189742390 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107909565 | ATCACAAATTCCATA[A/C]CCATCACATACAGCA | 10451 |
rs189746448 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107581484 | GCAAAACCTGAAGTA[C/G]TAACATTACCTAATA | 10451 |
rs189747692 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107929992 | CTAAAAAATTAAAAT[A/T]ATTGAACTCATGGAG | 10451 |
rs189749578 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107892937 | GTATGAGGTTTAACA[A/T]TAGGCTGAGCACTAC | 10451 |
rs189759956 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590096 | GGGAGAGACAGCCTA[A/G]GCTCTGTTCTGGCTT | 10451 |
rs189760898 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107586671 | ATTGATTAATTATTT[C/T]GAAAAAGAAAAGGAA | 10451 |
rs189765713 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624333 | CCAAAGTCTCACTGG[G/T]TGGGATGTACATGAT | 10451 |
rs189766265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107854700 | GTATGTCATAATGAC[C/T]TCCCTGACCTTGAGA | 10451 |
rs189767773 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573069 | CTCTTCTGGGAAGAA[C/T]AGCTCTTGGTTTTGC | 10451 |
rs189768405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872338 | CTATCATAATTAATA[C/T]ATTCTTTGGCAAAAA | 10451 |
rs189769360 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107663379 | TTACTCTTAAAAAAA[C/T]AAATATGCATAGTAT | 10451 |
rs189781746 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107601748 | CACAAAATATTCTTA[C/T]ATGCTAACAAAAGTA | 10451 |
rs189782712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107837573 | AAAAAAGAGCCCAAA[C/T]AGCCAAAGCAATCTT | 10451 |
rs189783446 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107701939 | ACATCTTCCTGTCTT[A/C]TTCTGAGCCCTCCAA | 10451 |
rs189787912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107669634 | TGTTTTTCCTATTTA[C/T]GATTGTTTAAATTGG | 10451 |
rs189791389 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107622997 | GAAAAAAACCAGCAA[A/G]GAGGAAGTGATCAGG | 10451 |
rs189798512 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107669523 | AGAATGCCTGAAAAT[G/T]TCACCATGGATCCAT | 10451 |
rs189798651 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649012 | TCCAGGAGGAAGGTA[A/G]TAACTCCCAGTAATA | 10451 |
rs189808359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107708044 | TTTCATAAGTATTTA[C/T]TGAGTAACTACCATA | 10451 |
rs189809017 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107688312 | CAGTGTAAAAGCCCA[A/C]GCCTGGTTAAGTTAG | 10451 |
rs189819493 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107722439 | GTAAAACTCCTAAGA[C/T]AAAAATTGGAACAGC | 10451 |
rs189821105 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107708188 | ATTGACATCACATTT[A/C]GTTGAGGAAGAAAAA | 10451 |
rs189823062 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107760680 | TTCAAAATTTTAAGG[G/T]GATTGGGCCCAACAC | 10451 |
rs189834891 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107735409 | CTTCAAAAAATCAAC[A/G]AATCCAAGAGCTGGT | 10451 |
rs189894613 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107953571 | AGTATATTATTGCAC[A/T]TGTAAGTATCCGCTG | 10451 |
rs189904737 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107888322 | AGTGTTTAAACTGTA[A/G]CTCAGATCAGCAAAA | 10451 |
rs189905907 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107905863 | AAAGATACATGTAAT[A/T]ATCAAAAAACTAACA | 10451 |
rs189907187 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107918676 | GGCATATATATATAT[A/T]TTTTTAAGGCATATA | 10451 |
rs189912450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107956721 | ATAATCAGATGACTG[A/G]ATGGCCCAAGGTGCC | 10451 |
rs189918271 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | VAV3 | GRCh38.p7 | 1:107891725 | ATGCCTGTAATCCCA[C/G]CTACTTGGGAGGTTG | 10451 |
rs189922000 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107865146 | CACAGGTGGCTGGGG[G/T]CAGGGTAGGGTGAAA | 10451 |
rs189923408 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107912868 | TTGAACTGAAAGAAA[A/C]ATCTCAGACACTTTT | 10451 |
rs189923930 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107848204 | TGTAGTCCCAGCTAA[G/T]TGGGAGGCTTAGGCA | 10451 |
rs189927958 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107804221 | CTTTTAATTGGAGAA[A/C]TGCATCTGTTTATAC | 10451 |
rs189932199 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107831401 | CAGGGAAATGCAAAA[C/T]GAGCAAAGATAAGCA | 10451 |
rs189941826 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107812663 | ATAACACCTACTAGA[A/T]ATCTACATCCAAGGT | 10451 |
rs189966094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107846986 | ATCTTCTCAGCACCA[C/T]ATTGCACTTATTCTA | 10451 |
rs189980647 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107811901 | AGATTAAATAATATG[A/G]CCTGAGATTTTGGTT | 10451 |
rs189986239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107955055 | CAGTGATAATCATTA[C/T]AGTAAAAAATAGTTA | 10451 |
rs189996608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107763687 | TAAAGTCAACATAAT[A/G]AAGGAATATTAAGAT | 10451 |
rs190008700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780949 | AGGCAAAAATCTGTT[C/T]CTAAATTAAGGTAAT | 10451 |
rs190011801 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107576963 | ACATCCCAGCTTATT[C/T]TCAAAAGGAGAAAAG | 10451 |
rs190027696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654600 | ACTAACTCTCTCCCT[A/G]ACCTTCCTTCCTTTT | 10451 |
rs190034328 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107576318 | TCCGTATGAGAAGCC[A/G]TACATGGAACTCAAA | 10451 |
rs190035295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107648117 | ACAAAGGGAACACTC[C/T]CCATCAATAATTTTT | 10451 |
rs190046770 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107597287 | TCCCACTGCCATCAA[C/T]TTAATATCTCTGTTC | 10451 |
rs190055562 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618479 | TTATTAACAGAAGAA[C/G]ACCGTAAGATTTTGG | 10451 |
rs190062123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693143 | TCATACCTATTCATT[A/G]TTAACGTTGGAAAGT | 10451 |
rs190063595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107687684 | GGAACTCTATATAAA[C/T]AACATCAAACAACAC | 10451 |
rs190069484 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107721782 | TACACAAACTAAGTA[A/G]CAATCTCAGCCTAGC | 10451 |
rs190074138 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107724871 | TGAGCACAGGCCAGA[C/T]AGTAAATGCCATTTG | 10451 |
rs190090231 | snp | A/C | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756715 | TCTGTCTTTTCTATT[A/C]ATAATTTTCGTATTT | 10451 |
rs190092963 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753694 | CCTCCCCAGTAGCTG[C/G]GACTACAGGCACGTG | 10451 |
rs190151004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903326 | CTTTGAAGTAATGAA[C/T]GTAAAACACAGCTAT | 10451 |
rs190161106 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107882110 | TTAACTGAGGCAATG[A/G]AAGAGGAAAAATCTC | 10451 |
rs190161471 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107934160 | AATTATAAGAACTCT[A/G]TGGTTTATTCTTTAA | 10451 |
rs190162942 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862399 | TATTCCTACAGATGT[G/T]CATAAGCCATTAAAA | 10451 |
rs190167843 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895670 | GAAAAACTGGTATTA[C/T]TGGCCACGTCACTGA | 10451 |
rs190179464 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107826917 | AGCACTAAATATTAT[C/G]ACTTGTTTCAGTTTT | 10451 |
rs190190406 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107808878 | TTTATCCATATGCCT[A/T]ATTATTCCTGATAAT | 10451 |
rs190192829 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107926759 | ATTTAAACCAGCCCT[G/T]GCCAGAGGGGAATTT | 10451 |
rs190199166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107631939 | GCCGCAATAAACATA[C/T]GTGTGCATGTACCTT | 10451 |
rs190205881 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107863692 | TACGTATATCTTGGT[A/G]TGTCTGTAAACCTCT | 10451 |
rs190215298 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656141 | ATATATTCAATTGAT[A/T]CCTGCACTCCCTTGC | 10451 |
rs190219671 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107890757 | TCTAGTAAATACCTT[A/C]ATTTCTGTGCTCTGC | 10451 |
rs190221897 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107825611 | ATATTCTGTCAAACT[G/T]GTCTACTCCCCTACC | 10451 |
rs190225584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107696028 | TTTTTTATTTTATTA[C/T]CTTTAATTGACACAT | 10451 |
rs190225998 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107850439 | ACATGGTTGAAGCTG[A/G]AAACCATCATTATCA | 10451 |
rs190228485 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107829856 | TTTAATCAGAACAAA[C/T]AAGGAGCCTTTCATA | 10451 |
rs190231614 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107675334 | TCTTCATAATAATAC[C/T]AGGAGATGGCTGCTA | 10451 |
rs190233161 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713445 | TAATCTCCTTGCAAT[A/T]CACAAGTACCATTGA | 10451 |
rs190242722 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107791670 | AGAATTTTTTTAAAG[A/C]TTTCCAGTGATTCTA | 10451 |
rs190249467 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107726578 | AAAGCTAGCAGTTAT[C/T]AAGCTCTCTGGATCA | 10451 |
rs190251352 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107767294 | AGTAAATACATGTCA[C/T]AGCCAGGATATGAGG | 10451 |
rs190253613 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107739837 | GGAAGGCTCCCCCTC[A/T]GGCCAACTCTTGATA | 10451 |
rs190257874 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107784012 | TTGCAGTGAGCTGAG[A/G]TAGTGCCACTGCACT | 10451 |
rs190271490 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107600355 | CCAGCTCCTTGTTTT[C/T]CTTTTCATAATTACA | 10451 |
rs190272282 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107597204 | AATGTTTCTATTGGA[A/G]CGCCTTTTTAAAAAT | 10451 |
rs190292898 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672872 | GACTTATAGTGAAAA[C/G]AACAATACAAGGTTG | 10451 |
rs190305953 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107647633 | TTCTTGGGTAGGACC[A/C]TAAAACATGTACATT | 10451 |
rs190306698 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107710027 | AATGTAAAATAATAA[C/T]ACATATGATTTTTAA | 10451 |
rs190325331 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | VAV3 | GRCh38.p7 | 1:107738026 | AATAACTGTGCAGCC[A/G]TAAAAAAGGATGAGT | 10451 |
rs190357544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107715261 | AAGTGAGAACATATA[C/T]GTGTGCATTTTAATA | 10451 |
rs190372959 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107743561 | AATACTTAAATTCAA[C/T]TGCAATGGCTCCCTC | 10451 |
rs190390683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107898787 | GCAACAGATTATATA[C/T]TATACATGAACATAA | 10451 |
rs190394760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107944122 | GAGTGAAAAACCCAA[A/G]GAGCAAAGATACAGA | 10451 |
rs190396407 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965712 | TGCGTGTGTGGAGAC[A/G]CCTGCGGAAACCGCC | 10451 |
rs190405664 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107790514 | CAGAGGAGAGGAGAA[A/G]AAGGAATATGTCTCC | 10451 |
rs190405868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906249 | CTAAGCCAAGGCTTG[C/T]TTTGTTTTGTTTTGT | 10451 |
rs190409316 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107924812 | ATTAAATATTAAACA[C/T]AGAACAACACAACGA | 10451 |
rs190423106 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107945736 | CTGAGGCGGGAGAAT[C/T]GCTTGAACCTGGGAG | 10451 |
rs190446515 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107943500 | CTTCCCAGCACTTTG[C/G]GAGGCCGAGGCAGGC | 10451 |
rs190451696 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107905197 | GTATTGCACAACCTG[A/G]TAAGTCAGCCTTACC | 10451 |
rs190456196 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107907675 | TTCTCTCTCTCTCTC[A/T]CACACACACGCGCTC | 10451 |
rs190459004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107660183 | AGGTCATAGCATGTT[A/G]AACCCTGCAATGCTC | 10451 |
rs190459968 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107843821 | ATCCTAGGATAAAAC[A/G]TACCCCTACAGAGCG | 10451 |
rs190468855 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107864067 | GAGCTTATATATAAA[C/T]AAAAGGTATGAGAGA | 10451 |
rs190469089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107651691 | CTTCATTTCTACCTC[C/T]CAGTTCAAGCACTGT | 10451 |
rs190469479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700364 | GTTACATAGGTAAAC[A/G]CGTGCCATGGTGGTT | 10451 |
rs190469662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107869147 | CCCATTCCTGAACCA[C/T]CACTATGTGGTCAAA | 10451 |
rs190477867 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107678420 | TATTATAGACAAAAG[C/T]TCATTTACTAAAACC | 10451 |
rs190480027 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107627198 | TAGGCAGCGTTTGTT[C/T]TCTGTAAACCCCTAT | 10451 |
rs190480229 | snp | A/C/G/T | 0.00319106 | 0.0398404 | intron-variant | VAV3 | GRCh38.p7 | 1:107716250 | AAAAGAACTTTAAAA[A/C/G/T]GTTAAATGTGTTTAT | 10451 |
rs190482600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807419 | CTTTGCTCTTATATT[A/G]GAAACAGGACTTTTA | 10451 |
rs190491032 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729103 | GCCTTAGCAAACTAC[G/T]TATGACCTCAGGTAT | 10451 |
rs190505692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107744463 | AGAAATTCTAGGCAA[A/G]AGGACCTTTCATTTC | 10451 |
rs190513586 | snp | A/G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107762409 | AGTCAAAATGAATTG[A/G/T]GGACACATCCTGACA | 10451 |
rs190514821 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107585567 | GTCCTTCTGCTCTGG[C/T]CACATTGCCCAGTCA | 10451 |
rs190523617 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107801354 | TGTGAAGAATATCAC[C/T]GATATTTTGATAAGG | 10451 |
rs190551474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107668966 | CTTCAACTCTTTCGC[A/G]ATACGGGTGTGGGGT | 10451 |
rs190557486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107622662 | GGAAATTCTCCCAAG[C/T]TACAATGCCCTAAAC | 10451 |
rs190588520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699362 | ATATCCAGGTCACAC[C/T]GATGCAAGAGGTAGG | 10451 |
rs190604942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107673833 | TGTGTAACAAAAGTA[C/T]ACAGGGTGATTAGCT | 10451 |
rs190610319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107685617 | GCAGTGGAATAAACT[A/C]TGAACTGGTGTATTT | 10451 |
rs190613106 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107803104 | ATTTATCTGTTTCTT[C/G]TAGTTTTCCCAATTT | 10451 |
rs190617195 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107728642 | ATATGTATATGTATA[C/T]GTATATGTATTGTGT | 10451 |
rs190628549 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107761365 | GTCACTGCACTCCAG[C/T]CTGGGTGACAGAGTG | 10451 |
rs190630404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107706191 | GACTGTAGGAAAAGC[C/T]TGAGATACTGATGAG | 10451 |
rs190638665 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720060 | ACCAGGCCCTGTCGT[G/T]GGGTCGGGGGAATGG | 10451 |
rs190640383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940411 | ATCCAGAATTTGGCA[C/T]AACCCAGAGCCATGT | 10451 |
rs190644627 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107733747 | GGGACTATGTGAAAA[A/G]ACCAAATCTAAATTT | 10451 |
rs190644636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959423 | TATCAGGTGTTTGCC[C/T]ACCACATCACCAAAT | 10451 |
rs190648680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751530 | TTTTTTGAGCATCTA[C/T]TACGTGCCAACCACC | 10451 |
rs190649411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107733604 | CTCATACACAAGCTT[C/T]GGTAGCCGATTCAAT | 10451 |
rs190653230 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921320 | AAACTGCATCACATA[C/G]TTTAGTGAAACACAC | 10451 |
rs190661301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107883218 | AGCTCATAAATGCAG[A/G]GCTAAATTGTAAAAA | 10451 |
rs190666173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107957423 | AACTTTCTACAATGA[C/T]CAGGCTTCATACCTA | 10451 |
rs190666981 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963953 | AGGAGCCGACCGGCA[C/T]CACAGCACCTGAGCA | 10451 |
rs190669515 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786336 | AAAAAAAAGCCATAT[A/C]CTGGGCTGATTAGAA | 10451 |
rs190669984 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107767636 | ATAGAATCAAAACAC[A/G]AAGAACTGTTCAGGT | 10451 |
rs190693479 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107610201 | CACTGTAACTCTAAG[A/C]GGAGAGATAGCAGGC | 10451 |
rs190708818 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587645 | GCCCATGCTGGAGTG[C/T]AGTGGCACCATCTTG | 10451 |
rs190718805 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881876 | TTGACGCTTAAAAAA[G/T]GAAACATTTGAAGGT | 10451 |
rs190720362 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107888089 | AAAGTAAAAAGAAAG[G/T]ATTAATGGTTACTTT | 10451 |
rs190726172 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107631110 | TTTGTCAAAAAGGTA[C/T]CCCTTATTTGGTAAC | 10451 |
rs190727078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819289 | GGGAGGGAGAGAAGA[A/C]ACAATCATGGGTCAA | 10451 |
rs190727195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107845029 | ACACCTCCCAGCAGG[A/G]GTCGACAGACACCTC | 10451 |
rs190733092 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655829 | AAAGACATATTAGTC[A/G]TCAACAGGTATATGA | 10451 |
rs190734559 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107847346 | AAATCGCCACCCTAA[C/G/T]ATCACGGTTAAAAGA | 10451 |
rs190765507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107820956 | TAGATGACTGAAGGT[A/G]TAAAAAGGCAGCTGA | 10451 |
rs190837281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107853968 | GGGTAACTGTATTTT[C/T]TTTTTCTAAGTTGGG | 10451 |
rs190840562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655111 | AGCACAAAGTTCACA[G/T]GCACAACTGTTCAAT | 10451 |
rs190851263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107836414 | CAAAATACTTGGGAT[A/G]TAATGAGAGTAGTTT | 10451 |
rs190853726 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107817540 | AGCTCATGAGGAGCA[A/G]AGGAGAGGCAGAATC | 10451 |
rs190864006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107797469 | AGGCATGTAAACAAA[C/T]CACTGCAATCAAATT | 10451 |
rs190867950 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107708530 | TGTTGACACTCTTAG[G/T]GCTTCATATAGCTTT | 10451 |
rs190868612 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107694651 | GTCTCTACGAAGGTG[C/G]AACCAAAACTGTACA | 10451 |
rs190868757 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107660501 | GCACCAGGCCAAGGC[A/G]GACCACTGGCCTTAT | 10451 |
rs190881807 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723216 | AGCAAAACAACAGTA[A/T]CAACAAAAAGAGAGC | 10451 |
rs190888550 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107736445 | AGATGACACGATTGT[A/T]TATTTAGAAAACCCC | 10451 |
rs190896280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107718980 | CCTATTCAATAAATG[G/T]TGCTGGGAAAACTGG | 10451 |
rs190899689 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107754942 | AATCCTCAGTTATAG[C/T]AGCCAGTTCACAGCA | 10451 |
rs190900844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700713 | CACTGATGGGCATTT[C/G]GGCTGATTCCGTGCT | 10451 |
rs190912378 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107729629 | TTACTTACATTTCTG[A/G]TCCTGAATTTTCTCA | 10451 |
rs190915147 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107750800 | TATTTAAAAATATAT[A/T]CCAAAAATTCAATTA | 10451 |
rs190916844 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790023 | AAACAAAACAGATGC[A/T]CACTGGCTAGAAGAC | 10451 |
rs190928034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107785133 | TCTTCATGAGACATT[C/T]GGGCAAATGTCCACT | 10451 |
rs190934362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107935147 | AATTCCTAAGGTCTT[C/T]TCCATTTGGGGGCAA | 10451 |
rs190939050 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591920 | AAAATTGCATTGATG[C/T]GGTACTATTTTTTAA | 10451 |
rs190940053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107938872 | AATAGACCATAACCT[A/G]CTCTTGTACCAATCA | 10451 |
rs190945083 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107614658 | AAATATCATTCAATA[A/T]GATTCTACAGGCTGA | 10451 |
rs190945443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897700 | GCAGTTCCTCAGAAC[A/C]GCTTATCTGAGACAG | 10451 |
rs190950060 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571451 | CAACAGGAAGACTAA[A/C]CACCATTTATAAGGA | 10451 |
rs190952420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902845 | CAACTCATTTATCTA[C/T]ATCCATACCCGTATT | 10451 |
rs190970141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858065 | TAAATGTAATAAAGA[A/G]TATGCTTATACATTT | 10451 |
rs190972636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107861303 | TTTGTAAAAGCCAAC[A/G]CTAATTAATATCATC | 10451 |
rs190982862 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107798227 | TATTTATTCTAATTT[C/T]AACATCCAAAAGCTA | 10451 |
rs190989942 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107826306 | GCAGATTTGAAACCT[C/G]TAAGATTGAAAATTC | 10451 |
rs190991970 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107823474 | AATGGGAATGGCTGA[C/G]ACTCCCCACGTGGGC | 10451 |
rs191023524 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793291 | CTAAAACCACAAAAA[A/C]CAAAACAGCCTGTCA | 10451 |
rs191062369 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107934418 | TTCTTCCTGTGAAAA[C/G]AGAAACAGAACAAAA | 10451 |
rs191067309 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107577608 | CTAACAATACAGTGG[A/G]CACACGCCTTTGCCT | 10451 |
rs191068796 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107954804 | TCCTCATCGCAGTTC[A/G]CATTCAGATAGGCCG | 10451 |
rs191077387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913737 | AACCTTGGCAGAGTG[A/G]AGTATTAAGGAGGCA | 10451 |
rs191089188 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593684 | ACCACTTCCTGGGAT[A/G]TATAAAATGCATAAA | 10451 |
rs191094182 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107848912 | TGCAAAAATCATAAA[C/G]ATTCCTATACACCAA | 10451 |
rs191096082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897434 | GTATCAGGAGCAACA[A/G]GGGAGGGAACAGGAG | 10451 |
rs191102150 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107832617 | AATTTATGAACTCTT[C/G]CAACTGTCTAATATC | 10451 |
rs191102446 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107876868 | CAAAAAGTGAGCAAC[A/G]TATTAGCTAATTATT | 10451 |
rs191106252 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107813530 | GTGATATTTTGTTAC[C/T]ACCATAGAATGGATA | 10451 |
rs191106372 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107857586 | ATTTCAACTCTTTTC[A/C]ATTTCTGTTTCACTG | 10451 |
rs191114863 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794644 | TTAGGACTCTGTTAC[C/T]TGTGGCCTTAAAATC | 10451 |
rs191124711 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107643419 | AATGTGCAATGAAGG[C/T]CTCAGTTCACGATTT | 10451 |
rs191125590 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107932244 | CACAAGTTCAAGAGC[A/G]GGCATTAAGACATAC | 10451 |
rs191126163 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107637845 | GTATTACATGAAAAT[G/T]AAACAATATATAAAA | 10451 |
rs191130906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107679332 | TCAGAAAGGACTCTT[A/T]TCAATTTAATCATTA | 10451 |
rs191131522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107952202 | TCCTTAGCAAACTAA[C/T]GCAGGAACAGAAAAC | 10451 |
rs191136571 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911060 | TCAACACCACCAGAC[A/G]AATAAAATGTTACTC | 10451 |
rs191145877 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107611657 | GAGGAGAGTAAAGAA[C/T]TTCAAAATATTCTGG | 10451 |
rs191149714 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107735917 | AAAAAAAGAGAATTT[G/T]AGACCAATATCCCTG | 10451 |
rs191154814 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894465 | AATTAAAACAAGCTG[A/C]ACTCTCATAATAAGG | 10451 |
rs191158056 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107716381 | GCCTGTAATCCCAGC[A/C]CTTTGGGAGGCCGAG | 10451 |
rs191159998 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107718761 | CAAGACAATCCTAAA[C/T]AAAAAGAACAAATCT | 10451 |
rs191164494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107874421 | CATGTCTTCTCTGAG[C/T]CACCCAACCAAGTAT | 10451 |
rs191164608 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856235 | GATGGTACTGATGGC[A/C]GTCACAGAAATGTGA | 10451 |
rs191194487 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107939313 | TTCTTGCCTTTACAC[A/G]GATGGTCCTAGGCTT | 10451 |
rs191195699 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107913882 | CTCACTGCAACCATC[A/G]CCTTCAGGTTCAAGC | 10451 |
rs191201697 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107877923 | GTGTGTGGCTCTGTG[C/T]ACATATAGGAACAGA | 10451 |
rs191214200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776016 | ATTACCCTCAGCAAG[A/T]AACTAGGCTTTTCAA | 10451 |
rs191258685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599898 | ACTCCTTACTTATAA[C/T]AGACAAGTGTGTTAT | 10451 |
rs191274030 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107835474 | GATGTGCGGTTTGTG[C/G]GCCAGTGTGAGAGCT | 10451 |
rs191293144 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107622461 | TTGCTTGGCTCCTAA[C/T]TCTGTAAAAAGGAGA | 10451 |
rs191293743 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107797000 | AGTGAAAATACTCCT[A/G]TAATAACTATATGAC | 10451 |
rs191294869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667655 | ATCCTCTATAAATTA[C/T]TTAAAATAGCAACAT | 10451 |
rs191302179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107646690 | CTTTTGCTCACATTA[C/G]TAATTGTGCTTGGTC | 10451 |
rs191314817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686760 | TGAAAATTAATTCCT[C/T]GTATCATAGGCTTAC | 10451 |
rs191316765 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107726804 | AGATGGAATAAAGCC[G/T]GCTAATTGAATTTTA | 10451 |
rs191317162 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107740689 | GTGGTAACATATATT[A/G]ACTAATTCTCTAGGC | 10451 |
rs191323028 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107707351 | TAACTTGCAAATCAG[G/T]AGCAGCGTGATCTTA | 10451 |
rs191323376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721095 | ATGTCCAGAGTTCTA[A/G]GGTGGACTGGAGAAT | 10451 |
rs191325355 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107759321 | AATTCTATTCTTTTA[C/T]TCCTTAAAAGTTACT | 10451 |
rs191335606 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107776667 | AAACATGCCTGATCC[A/T]TGTCATCAGTTCCTT | 10451 |
rs191345470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107828264 | TTTCTGCCTTTCAAG[C/T]GTACAAGATTCAGTG | 10451 |
rs191353568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107810651 | AGGAAATCTAGGAGA[C/T]AGTTTTTCCCTCAGT | 10451 |
rs191354751 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588182 | AAATAAAAAAGGGAA[A/G]CCCAGCATCACTTAC | 10451 |
rs191363076 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107791109 | TGGCAAAAATGGACA[C/G]CAAAATATATACCTC | 10451 |
rs191365703 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592385 | TGTCCCATTATTAGG[A/G]ATGTTAACTTCAATC | 10451 |
rs191370563 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107618589 | ATCCTTAATATGTGC[C/T]AGACACTGCTCTGAG | 10451 |
rs191383424 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107637380 | GTAATCCTAGCACTT[C/T]GGGAGGCTGAGGAGG | 10451 |
rs191384452 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107665476 | TTGGTACAGCACTGC[A/T]AAACACTTTTGTGTG | 10451 |
rs191384646 | snp | C/G/T | 4.95432e-05 | 0.0049769 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107704624 | GCTCCACACTTAAAA[C/G/T]ATAAATAGCCTTGAT | 10451 |
rs191421738 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107670982 | AATTTAAATGGAAGA[C/T]GCATAAAATATTTAA | 10451 |
rs191425370 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107958964 | ATTGTGTCATAAGAA[A/C]ATAAACTATATCTAG | 10451 |
rs191437633 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107708989 | ATTGGTTTTGTTTCT[C/G]TAAAGAATCCTAATA | 10451 |
rs191440891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759066 | GGCCTTTAACTGTGC[C/T]GGTTCTGTACCTTAC | 10451 |
rs191450042 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107955509 | TGGAAGGGAGACGGA[C/T]AAGGAAAAAAAACTG | 10451 |
rs191450738 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107920804 | TCAGCACATTTTCCC[G/T]TACGATTATTTGTGT | 10451 |
rs191456248 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107736886 | AAACAAAAAAGAGCC[C/T]GCATTGCCAAGACAA | 10451 |
rs191457975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915672 | AGTTGATGAGCACCC[G/T]GTGGACAGGGGCTGT | 10451 |
rs191472372 | snp | C/G/T | 5.38327e-05 | 0.00518787 | intron-variant | VAV3 | GRCh38.p7 | 1:107765049 | GTTTATTTTGCTTTA[C/G/T]GTCATAAACTAAAAA | 10451 |
rs191477004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107772069 | GCAGCTGGTAAAGAA[A/G]AGTCTTTAATATACA | 10451 |
rs191478633 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107781969 | ACTATTAAGCGAAAA[A/G]TCTAACTTTGGGGAG | 10451 |
rs191495265 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107888710 | GTGATCCCCCCGCCT[C/T]GGCCTCCCAAAGTGC | 10451 |
rs191506319 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107853204 | GCTCTGGAATCCGAC[C/T]CCATGGGTTCAAAAT | 10451 |
rs191514094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107848424 | GGCTGGTTCAACATA[C/T]GAAAATCAATAAACA | 10451 |
rs191525304 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107816631 | ATGCTTGTCTCTTGA[C/T]TCATTTATTTTTGCT | 10451 |
rs191534197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618030 | CACCTCAGGCATTAG[A/T]CTCTCATAAAGGAAG | 10451 |
rs191535121 | snp | A/C/T | 0.00159649 | 0.0282165 | intron-variant | VAV3 | GRCh38.p7 | 1:107812967 | TCTCTACTAAAAATA[A/C/T]AAAAAATTAGCCAGG | 10451 |
rs191539689 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107671655 | GGGAGACACATATGT[A/G]CAAAAGGAAATAAGA | 10451 |
rs191543912 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107628117 | TTGATGATAAGGAAG[A/G]ATTTAGCTGACAGAA | 10451 |
rs191548180 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107652203 | AACCAAGATGGCCAC[A/G]GGAGTGACCTCTCCT | 10451 |
rs191551730 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107691112 | GTGACTATACCATTA[A/G]ACAGACTGCCTCCTT | 10451 |
rs191553081 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945082 | CTGCTATTTGGCTCA[A/T]GATGATTCTATGCCC | 10451 |
rs191568112 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107926011 | CAAGGGGCCAGGTGC[A/G]GTGGCTGCCTGTAAT | 10451 |
rs191571884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709293 | CAGGAAAATTAATGC[C/T]AGATATTCATAGCTG | 10451 |
rs191575621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107889416 | TGAAGAATGAATATA[C/T]AATTTATTGTCCAAA | 10451 |
rs191579178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107723764 | TGTCTTCCATACTTC[C/T]ATATTTCTCTTGGTG | 10451 |
rs191581411 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107906890 | ACTGTTCCCTGGCTT[A/G]GAAAGTTAGAATTAA | 10451 |
rs191585046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737036 | AACAGAATAGAGGCC[A/T]CAGAAATAACACCAC | 10451 |
rs191587188 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107867591 | AAAGGTAGCCTTGGA[A/G]CAAGCTATCTTTGTT | 10451 |
rs191592542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825093 | CTTATGTGCTGTCTA[C/T]GGCTGCCTTTCTACC | 10451 |
rs191599253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805867 | TTTCCAGCATTAGAT[A/G]GAACCTTAAACCCAG | 10451 |
rs191602437 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107833312 | TCCCTTAAGCCAAAA[C/T]ATAACTCAAGGCCCT | 10451 |
rs191620266 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572296 | AAATGAATAAAGGAC[C/T]CAGTTGTGCTTTCCT | 10451 |
rs191643870 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107615182 | CACACCTAACCATCT[C/G]ATCTTTGACAAAGCT | 10451 |
rs191684779 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107658065 | GGCACAATACTTCAA[C/T]ATCTCTTTCTAATGA | 10451 |
rs191690822 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690172 | TCTGATTCTTCCCAT[A/G]GAAGTGTTTTTAGGT | 10451 |
rs191697623 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698624 | GTATTTGCTTAAAAA[C/G]ATTTTAAAATCTAAG | 10451 |
rs191698917 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107695343 | CAGGGAATTAGGAAA[C/T]TTTTGAGTTGTTCAA | 10451 |
rs191699788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676007 | AACAGAGGATCCTAC[A/G]AATGGAAAAAGGACA | 10451 |
rs191707410 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107723676 | AAAGCTGCGCTAGTA[A/C]CATTAAGTACTGCTG | 10451 |
rs191708319 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107714182 | CCAATACTATGATGG[A/T]CAGGAATCACTCTCC | 10451 |
rs191711181 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107726232 | ACATACAGATAAATC[A/G]ATCAACCTATAAAAA | 10451 |
rs191715909 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107780411 | TTAAATATACTCTGC[C/T]AGCAACTTTACCCTT | 10451 |
rs191720091 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107935991 | CAGTGTGTGAGAGAT[A/G]AGGACACATTTATGC | 10451 |
rs191721429 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107727467 | GCATAAATTAATTAT[C/T]AGGCATTTAACCTCC | 10451 |
rs191725028 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755179 | GGACTCCTATATTTA[C/G]ATTCAGACTGCTGGG | 10451 |
rs191726842 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107758697 | TAAATCAGATCCTGT[C/T]TCTACCCTACTCAGA | 10451 |
rs191737050 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599258 | CATGTTTCTAACTGG[A/G]TAGAACTAAATAGTG | 10451 |
rs191738693 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107742453 | CCTTGGGCCACTAAA[A/G]GTACACCAAAATAAA | 10451 |
rs191746604 | snp | G/T | 3.49926e-05 | 0.00418271 | intron-variant | VAV3 | GRCh38.p7 | 1:107760737 | CTTCATTAATATTTT[G/T]TTGAGTGAATAAATG | 10451 |
rs191747525 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621819 | CATTCCTCTCTCATA[C/T]TTAGGTGTCATCTGA | 10451 |
rs191751543 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107778622 | GAGAACCCCACTAAG[A/T]CCTGCTTGGATCCTC | 10451 |
rs191753412 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107929685 | AAAAAGTGGAGGGAC[A/G]AAGTTAAAAAGTGTA | 10451 |
rs191757728 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107578816 | AAGAAATAAAACACT[A/G/T]TATTTCTCCAAAATT | 10451 |
rs191762638 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107941197 | CCTATTTGTAGAACC[C/T]TTCTTTCCCAGCCCG | 10451 |
rs191763428 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107862552 | TAGACAAGTAAATTG[A/G]CTATTAATATATCAC | 10451 |
rs191766119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107865276 | AGGTCCCAGTTGAAA[C/G]TGAGGGAATGTGCAG | 10451 |
rs191767565 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107891952 | TCCCTTTAAACTCCA[G/T]ACTATAAAATGTAGA | 10451 |
rs191774587 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921974 | TTGTGTAAACCAGGC[A/C]TTCAACCTGCCTCAC | 10451 |
rs191784105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831942 | CTTGACCAGTCACTG[A/G]TACAGAACCTAAACC | 10451 |
rs191787403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885773 | CCAGTAAGTGATGGT[A/G]CAAGGTTCTAACCCA | 10451 |
rs191787747 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107904739 | GTAAACTAAAAATGC[A/G]TAGAAGAAAAATTTC | 10451 |
rs191793073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950060 | TGGGAACTGAAAAAC[A/G]TGACTTGAGAGCTTC | 10451 |
rs191800008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793940 | TGACTTGCGTACTGC[C/T]GGACACGCCAAATCC | 10451 |
rs191802607 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107863180 | CCCTACTTTTCCCCT[C/T]GCCAGGTTTCCAAGG | 10451 |
rs191804016 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107846313 | GGACTAAATACGGAA[A/G]GGAAAAGCCAGTACC | 10451 |
rs191817867 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107828513 | TTGAATTTTTGACTT[A/G]CAAAAATCACGGGGT | 10451 |
rs191822271 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107811411 | TTAAAATAGGATGAC[A/G]CTCTGGAAAAGCCTC | 10451 |
rs191906029 | snp | G/T | 0.000199276 | 0.00997989 | intron-variant | VAV3 | GRCh38.p7 | 1:107603206 | TGGATAATATACCTG[G/T]AAGAGAACAGAGGCT | 10451 |
rs191930429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649981 | GATTAGAGAGTGACA[G/T]GGGTGTGTGTGGAGT | 10451 |
rs191939996 | snp | C/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689536 | CTTTTTTTTCTTTTT[C/T]TAACGAATACTTCTG | 10451 |
rs191957310 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107603942 | CCCAAGTAGTTGATA[A/C]CACCGGTGTGGTTGA | 10451 |
rs191960616 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107716858 | ATCCGGCTGTGAATC[C/T]GTCTGGTCCTGGACT | 10451 |
rs191967382 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107701845 | GGGACCACCTCAGCC[C/G/T]GAACTTCATTGTCCA | 10451 |
rs191980495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107745920 | GGGGAACTCAAGGGA[A/C]TCGTGTTGATACTAA | 10451 |
rs191981591 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107584725 | GTCTAGGATTATTGT[A/G]AAAAATAAACTACTA | 10451 |
rs191983043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107944504 | AATTCTTTGTTATAT[A/G]TTCAGTGCCTAATGA | 10451 |
rs191985421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731148 | TATTAAAATCTGAAG[C/T]CATCCTTTAAATACT | 10451 |
rs191987311 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107746376 | CTGCATAGACATTCA[A/G]CGGAACTCTAAAACA | 10451 |
rs191993123 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107906393 | AATCGGGCTGGGCAC[A/G]GTGGCTCACGCCTGT | 10451 |
rs191995105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858506 | ACAGCAGGAGGTGAG[C/T]AGTGCGTGAGTGAGC | 10451 |
rs191996821 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107878273 | CCTACAGATCAACAA[C/T]ACCATTATATCTAAG | 10451 |
rs191997489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781397 | GGTTACATTTTAAGC[A/G]TTCTCACCACAATAA | 10451 |
rs191998566 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107764818 | AGATGAGAAAATTAA[C/T]TGTACCTATTTCACA | 10451 |
rs192000818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107712504 | ATAACCTAAGAAATA[C/T]TAAAATGTTTTTAGA | 10451 |
rs192001200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107866712 | CTTGCAGCCCCAGCT[A/T]CTCGGGAGGCTGAGG | 10451 |
rs192006016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107926662 | AGCAAGCGCGAGGCA[C/T]TGCATTTAACTCAGT | 10451 |
rs192009665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781757 | CTTCCTGGTCAACTA[C/T]GTCGAACATCTAATG | 10451 |
rs192013427 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107842422 | TACCTCTGAATCATT[C/T]TGTTTCAGGTGTGTC | 10451 |
rs192016364 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945552 | GTCACGTCCAGGCGC[C/G]GTGGCTCATGCCTGT | 10451 |
rs192018513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739526 | TGAGACTCTCAGCAC[A/G]GCCCAGAGGCAACTG | 10451 |
rs192019658 | snp | A/C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107824200 | GTAATGTGGTGATGG[A/C/G]AACAAATGCCAGATT | 10451 |
rs192026505 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107840962 | ATCAAATAGCTTATA[C/T]GGGAAGGCTGGAGGC | 10451 |
rs192028620 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107805145 | CTTGGTAAAGCCTTA[C/T]TGGGGTTGAATCTGT | 10451 |
rs192033699 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774838 | TTACCCATAGAAATT[A/G]TAATAAAGCTGAGAA | 10451 |
rs192036448 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107948082 | TTTTGGATAGCTGTG[A/G]ATTTACTCCTTTAAG | 10451 |
rs192041945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107803779 | TTTGGTCTAGTGTAG[C/T]AGTTTAACTCTGCTG | 10451 |
rs192068715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107909053 | ATAGATTGATGTTCC[C/T]ACAAATAACTGAAAG | 10451 |
rs192077265 | snp | A/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107871800 | AAACAGAGGGAGAGC[A/T]TGGACAAAGTTTAGT | 10451 |
rs192079189 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107845454 | AGAGAATGAGTTTGA[C/G]GAATTGACAGAAGTA | 10451 |
rs192121801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107630401 | CCACTATTTAATGGG[C/T]ACTGTGCTAGAACTC | 10451 |
rs192131863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587488 | AGACTAGTAAAACCA[A/C]ATTCTTGGATCAGGG | 10451 |
rs192142134 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588685 | ATCATACTAGCAGCA[C/T]TTCTTATATATCTGT | 10451 |
rs192181545 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107633406 | TTATACGCACCAAGA[C/T]CTTCAACATTTTGTG | 10451 |
rs192189750 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107675572 | TCTTTCTTTCCTCAT[G/T]ACTCCTTTATTGCCG | 10451 |
rs192193057 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107921770 | AGTGAAATTATCTAC[C/T]GTAACATTCTAAGAA | 10451 |
rs192195506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107713612 | CAAGACATCATTTCA[C/T]GTGTCAGACTGGCCC | 10451 |
rs192197367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107960544 | GTTGACCTCTCATTT[C/T]ACTCAAAGTGAAATC | 10451 |
rs192219820 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625910 | TGACACAAACTTTTA[C/G]TCATTATGGCAGAAT | 10451 |
rs192221334 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107634277 | ACCAAAACAGTGAGA[C/T]AGACCAATGGAACAG | 10451 |
rs192221921 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107884306 | ATACCTAATTTTCCA[C/T]AATGTGATTATTACA | 10451 |
rs192223366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821166 | GTTATCATATCCTTA[A/G]AAGACAAAATCCTGA | 10451 |
rs192225618 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582786 | CATGGTGAATATCTG[A/C]CACATTTTCTTAATC | 10451 |
rs192226295 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107675711 | TCCCCACAAAACATG[C/T]TGTGTTAGGTTCTGT | 10451 |
rs192232956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107657622 | TATTACTTCTGATCT[A/G]GCATGACACTACCAC | 10451 |
rs192233190 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107845732 | TAATGAAATAAAGCA[C/T]GAACACAAGATTAGA | 10451 |
rs192242602 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107769237 | CTGTAAATCCCCTTA[C/T]CTTCTCTTCTTCCAT | 10451 |
rs192243631 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963635 | GTTCCTTCTTAAAAG[A/G]CGCTGCTCTGGTTGC | 10451 |
rs192259548 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107873445 | TCCCCAAAAGAGAGG[G/T]TGAAAATAAAGAAAA | 10451 |
rs192264382 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107670258 | CCAAGCAAGCACTGA[A/G]CTTGAAGTGCTTTGC | 10451 |
rs192265210 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107855841 | GCTCTTCCTTTGTGT[C/T]AACTCTAGAAAAATA | 10451 |
rs192267028 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107942711 | CTTGATATTCTAAGA[A/T]AACCTGATCTCTAGA | 10451 |
rs192267534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107839258 | TGACCAAATACAAAA[A/C]TGATAACCTATTTTA | 10451 |
rs192280999 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107820656 | GATAAATATTTGAGT[C/G/T]GACAGATGCCCCATT | 10451 |
rs192289165 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107801016 | AGAGATAGGGGTTTC[A/G]TTTCATTCTTCTACA | 10451 |
rs192309549 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107730222 | CCCTGAAGGAGAAGG[A/G]TGACAGCATTATCAT | 10451 |
rs192310873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107925580 | GAAATAAGCTAGTCA[C/T]AAGTGCACAAATGTA | 10451 |
rs192327317 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107764573 | CACCCTGGCTGGAGT[A/G]CAATGGTGCAACCAT | 10451 |
rs192337964 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889220 | TAACAATGCCCAAAA[A/C]CCTCCAAATTCTGTT | 10451 |
rs192351693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769565 | CTTAGTCCCAGGGCC[C/T]TAATGCCATTGTGTG | 10451 |
rs192358209 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788050 | AATTCATCCTTTTCA[A/G]ACTCTCTCAGATCCA | 10451 |
rs192385734 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107822851 | CTACATACCAGGCAC[C/T]TTTCTAGGTAATATG | 10451 |
rs192395262 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107585288 | CTGTTCCAGGCCACT[A/G]TCATCTCTTACCTTG | 10451 |
rs192431849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107573468 | TTTCATAACACCCCA[A/G]TTAAACTGGGGTTTT | 10451 |
rs192437355 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107937779 | AGGCTTGTAGTCCCA[A/C]TTATTAACACAATAT | 10451 |
rs192449758 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107900471 | AGTTTCTCTTCCACG[A/T]GCAAAGTGAAATGTT | 10451 |
rs192460635 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594722 | TACATTCTCTGAGTA[A/C]CTCCATGTACTAAAC | 10451 |
rs192467704 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107616639 | CAACAGAGTAACAGA[C/T]GCTTTTCTATTCTCT | 10451 |
rs192469481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107663616 | AAAGTGGTCAGAGCT[C/T]CAAAGAAAAAAATGC | 10451 |
rs192472348 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107702335 | TCCCCTCCTGCCTGG[A/C]CCCTCCCTTGACACG | 10451 |
rs192475705 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107662808 | GGGCAAAGCAATGAA[A/G]CTAAAAGTTGGTAAC | 10451 |
rs192475774 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860189 | GCAGTGGCATGATCT[C/G]GACTCACTGCAGCCT | 10451 |
rs192481765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936814 | CCTGGTTGGAATTTA[C/T]GCACTTATGCCTCAT | 10451 |
rs192486572 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107701189 | TTTAAGTGCCTTGTA[A/G]ACTCTGGTTATTAGA | 10451 |
rs192487655 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107609234 | TATACTAAATCCTAA[A/C]TATATTTTTTAATAG | 10451 |
rs192490543 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681544 | AGAAATAGGCTTACT[A/G]TATCAGCAGCTTCAA | 10451 |
rs192491716 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107956187 | CTGAGGAAGCTCTCC[A/T]CCAATTTTGTCTTTT | 10451 |
rs192494316 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107731798 | AATGGAGGAGCTTTA[A/G]TCTCCTCTTCAGAGA | 10451 |
rs192502939 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107917224 | TCAAGCATCAGCAGC[A/G]GCCTCACCAAAGTAG | 10451 |
rs192508299 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107790922 | CAAACTCCTGACCTC[A/G]TGATCTGCCCGCCTC | 10451 |
rs192514744 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879352 | CACTTGCAACAGAAC[A/G]GCTCATATACACAGG | 10451 |
rs192516691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107899981 | CTTTCTCCATAAAAT[C/T]CCTTTTTTTATATTC | 10451 |
rs192526528 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794708 | GACTTCTTTTTCTGG[A/G]TCTTGGGTATTTTGC | 10451 |
rs192539045 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107724552 | GAAAAGAAGTAAACC[C/T]AATAAAGTGATTCCC | 10451 |
rs192552066 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737824 | GATCTAGAACTAGAA[A/G]TACCATTTGACCCAG | 10451 |
rs192558033 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756394 | TCATAGGATAGATCC[A/T]TAAACGACTTCTTTA | 10451 |
rs192559393 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656793 | TGTGCTGCCTGCAAT[A/G]TCCTTTCCTCTCTGA | 10451 |
rs192561403 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107773454 | CATCTAATCCAGTGG[G/T]TTTCAACCCATGCTC | 10451 |
rs192563989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612343 | AAATTTCTAAGAGGA[C/T]AGTAATTTTCTCTCA | 10451 |
rs192566538 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107579491 | CAAAGTTAGTACACC[A/G]TTCAGCCCTCCTTGT | 10451 |
rs192588050 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107578775 | TCCATCCTTGTGTCT[C/G]TCTCTCTGGGACTAT | 10451 |
rs192597560 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107696543 | TGGACTCCTGATCCA[C/T]ACTGATCCAATCAGG | 10451 |
rs192602491 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940791 | GTCAAATTCAGAGAG[A/G]CAAAGTAGAAAGGGG | 10451 |
rs192607077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107904295 | CTAGATAAATGTATA[C/T]GTATGATGTGACTGA | 10451 |
rs192621380 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107839533 | GCAAAAATTGGTCCT[C/T]AGAGAAAAATTTATA | 10451 |
rs192637579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862885 | ATAGAAATGATAAAC[C/T]CCAAATTTCTAAGTG | 10451 |
rs192650354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107752335 | ACACCATAAATAAAG[A/G]ATAACTAAAAATGTT | 10451 |
rs192662076 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787722 | CCATTTTCTGAATGA[A/T]ATATTTCTTATTTGA | 10451 |
rs192691488 | snp | A/C/G | 0.00319074 | 0.0398324 | intron-variant | VAV3 | GRCh38.p7 | 1:107646107 | TCCTTAAAAAACTCC[A/C/G]TATTTTCCCTTGGCT | 10451 |
rs192711114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686255 | GCCCAGGTATGGTTA[C/T]GGACGCCCCACGGAT | 10451 |
rs192713411 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV3 | GRCh38.p7 | 1:107720364 | CTCCAGCCTGGGCAA[C/T]AGAGTGAGACACTGT | 10451 |
rs192719233 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107909855 | TGAAGAATACATTAA[A/C]TATTTCATAATAATA | 10451 |
rs192727080 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107872778 | TGCTTCAATCTCAAA[C/T]AGATATGTGATTTGG | 10451 |
rs192727747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107752151 | CAAACAGGTATATAG[A/G]CCAACAGAATAGTAG | 10451 |
rs192733556 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107838536 | ACTGTGGAGAGCAGT[C/T]TGGAGATTTCTCAAA | 10451 |
rs192740306 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107799495 | GTTGTCTGGCATAAA[C/T]ATAGAATAATATGTA | 10451 |
rs192759072 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107605281 | CCTTAAAAAGTGATT[A/G]GGTCACGGGGGCTCT | 10451 |
rs192767282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107956599 | TAATCTATTATTATT[C/T]GATTATAAATAAAAC | 10451 |
rs192780792 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107641539 | TTTACCTAAGTTCAA[A/T]AAAAGTTTCAACCAA | 10451 |
rs192782861 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107918034 | ATATTCTGTGAATAC[C/G]TTTCCTATGGGAACC | 10451 |
rs192786530 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107681867 | GGGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCC | 10451 |
rs192789816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880443 | GAGCTGGGATGTCCA[C/T]GGCATGCCAAAGAGA | 10451 |
rs192794702 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107843175 | TCCTGGGTGGGCATT[A/C/G]TAACTGACAGCTCTG | 10451 |
rs192800951 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717384 | GCATTTAGTGCTATA[A/T]ATTTCCCTCTATACA | 10451 |
rs192802268 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107773273 | GTCTTAACGCTGAGT[C/G]TTTTACCCACTCTAT | 10451 |
rs192808088 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107747156 | AAGTGCTGGGATTAC[A/G]GGCATGAACCATCAC | 10451 |
rs192812445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107814078 | TTTAGGTTGATTCCA[C/T]ATCTTGGCAATTGTG | 10451 |
rs192826180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595510 | AAAAATAAAGTGATA[A/T]CAGATTAAGAAAATA | 10451 |
rs192835089 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107640461 | GCTGAGGGTTGTTGC[A/G]CAAGGCGGAACAAAG | 10451 |
rs192846841 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107889814 | ATGACTAAGTTAGGT[C/G]CAGATTTGGAGAACA | 10451 |
rs192853189 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107849486 | AATGGGGAAAGGATT[A/C]CCTATTTAATAAATG | 10451 |
rs192860243 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107814688 | CTGATGTCTTAGCCA[C/T]AAAATTTTTGCAAGA | 10451 |
rs192861166 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107738034 | TGCAGCCATAAAAAA[C/G]GATGAGTTCATGTCC | 10451 |
rs192872446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773680 | TACTTTGGGACACCA[A/G]GGAGATGGTGATCCA | 10451 |
rs192907046 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962886 | TAGTGTAATAATTCC[A/T]TTAGGGCAAGTATCC | 10451 |
rs192909923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107667147 | CCTCTGCTCCAGGAA[C/T]GTATAGATGGTGGCA | 10451 |
rs192913759 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107930336 | ATTAAAACTAAAAAA[A/T]TTTTTTAAAGAATTA | 10451 |
rs192913888 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107707169 | AGTAGAAAGAAACTA[G/T]TAGAATTATTTGAAA | 10451 |
rs192928293 | snp | A/C/G | 0.00279242 | 0.0372774 | intron-variant | VAV3 | GRCh38.p7 | 1:107733859 | CAACCTAACAAGGCA[A/C/G]GCCAACATTCAAATT | 10451 |
rs192929548 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107893327 | TACTTTTCCCAAAAG[C/T]ACCCATCTCCAACTT | 10451 |
rs192935554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767962 | AGGAAGTAGGGTATT[C/T]CATAAATGGGAGTTA | 10451 |
rs192937312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107855341 | AAGTGCAGTGGCACA[A/G]TCATGGCTCACTGCG | 10451 |
rs192940412 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107791417 | GCTGCAATAGTTCAG[G/T]TGATAGAGTACACAT | 10451 |
rs192942753 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107820187 | GTACTGTTCACAGTA[C/T]CTATGATTTGGAAGC | 10451 |
rs192943239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107621045 | ATGGTATAAACTGAA[C/T]TGTTCTGGGTAAACA | 10451 |
rs192949029 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107577788 | GCCCTGCCCTCCAGC[C/T]CTGGAGTATTTCTAG | 10451 |
rs192953421 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107666778 | GTCCCTGTTCTATGA[C/T]CTTAGTATATATTAA | 10451 |
rs192968513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107931478 | AAGCAAATGTGATAA[C/T]CTAGATAACCGTTGA | 10451 |
rs192973670 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107893744 | AGATTTGGGTGGGGA[A/C]ACAGCCAAACTATAT | 10451 |
rs192980967 | snp | C/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107727065 | AGGATTTGATTACAT[C/G]ATTATTTTTGTATCA | 10451 |
rs192991943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760499 | AACTACAGAAGACTT[A/G]GTTGAAAAAATATTT | 10451 |
rs193001560 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107827345 | ACAACTTACAAATGA[C/G]GTCACTGTTCCTTGT | 10451 |
rs193016174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107573936 | GCAGAGGCCTGTGGG[C/T]TGAAAGCTGTAATAC | 10451 |
rs193025611 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107617287 | AAACCTGTACAATGC[A/G]TCTAATTTGTAGCTG | 10451 |
rs193036258 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107663062 | TTTTAAGAATATATG[A/C]GGTAAATCCACATTC | 10451 |
rs193042288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907296 | TATCTAAATTGTCTA[A/G]CACTGGGTGCTTATT | 10451 |
rs193056224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107868106 | TGTGCAATAGCACCA[C/T]ACTAGCAGACAGAGA | 10451 |
rs193061071 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107833774 | GTGAAGCTAGCAAAG[A/G]TCTAGGGAGTCACTT | 10451 |
rs193064203 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107725069 | GGTAGAAGACCCTGA[A/G]GACCTAAAGCAAGAC | 10451 |
rs193071292 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107795267 | GAAGTTACCAAGATA[A/T]CTAGCATCTAAATAA | 10451 |
rs193072440 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756774 | CTTGTATGAAGCCAT[A/G]GCATCCACAAGGGTA | 10451 |
rs193084187 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946016 | AGAGGAGGGAGTTGA[A/G]GCTGGGGAGGGCAGC | 10451 |
rs193094185 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107606088 | TCTCCCTCTTCCTTG[A/G]TTTACTAGCTCATCC | 10451 |
rs193095448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107653370 | AACAAACTTCTGAAA[C/T]AGAACAAGGGAAATG | 10451 |
rs193096906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907680 | TCTCTCTCTCACACA[C/T]ACACGCGCTCTCTCT | 10451 |
rs193102695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693118 | TTCAGAGAAGCTTGC[A/G]TAGTGGAGTTCATAC | 10451 |
rs193108126 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107842705 | TTTCTGGTTATGCAG[A/G]GGGTGTCATTTTTAC | 10451 |
rs193113658 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107805701 | GAGGTCATGGTTCCC[C/T]GTTTACTATTGTTTC | 10451 |
rs193179315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107598591 | ATTTGTAATCAGACC[A/G]ACCTTTAAAAGCAAA | 10451 |
rs193181645 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107645819 | GTATTAATTTAATAT[A/G]GGTTTTCTTCTCCCC | 10451 |
rs193190923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910342 | AAAATCCCCTCTTCC[A/G]TGTCCTGAAGAAGAC | 10451 |
rs193194382 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107714112 | GATAAATATGCAAAT[A/C]CTGGAGACCAAAGGA | 10451 |
rs193197761 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107741697 | AATCAAGAACATGGA[C/T]AGAGAGAGAAATATG | 10451 |
rs193201201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776862 | TAGCTCCAACCCACA[C/T]TTATCTCTCCCTTCC | 10451 |
rs193205394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107809684 | TAGCATAAAATCACT[A/G]TGCAAAGGCACTACA | 10451 |
rs193243411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107585875 | ATCCTGCTCTATGTA[C/T]TGACAGGATATTTAT | 10451 |
rs193248387 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107927220 | CCACTGCCATGAAGC[A/G]ATGGACTCAGTTCTG | 10451 |
rs193251742 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107890785 | TGCAAATCTGCACCA[A/C]ACTTAGCCATTTTTC | 10451 |
rs193253132 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107628756 | ATAGAACTAAAGTAG[A/G]GGACCACAAGTCTGA | 10451 |
rs193255144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672630 | ATATTTTCGATAAAT[A/G]TAAGATTGATCTCTC | 10451 |
rs193257046 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107709464 | TCTTATGTGAAAGAA[C/G]ACTGAAGAAAAACAT | 10451 |
rs193262634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107859650 | AAAGCTTTATTCAAA[C/T]TCAAAGAGGAGCAGT | 10451 |
rs199499435 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107695619 | ATGGGAGGGGATATG[C/T]AAGGAGAAGATGGTA | 10451 |
rs199500770 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107634687 | AGAGTGAACAGGCAA[A/C]CTACAACATGGGAGA | 10451 |
rs199532225 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582894 | GCATGTGTCTTTATA[C/G]CAGCATGATTTATAG | 10451 |
rs199547957 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107638545 | GACCTAAATAAATGA[A/G]GAGTATAGTATGTTC | 10451 |
rs199559448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107840918 | CATGTTCAGAGATGC[C/T]TTTAAAAAAAAAAAA | 10451 |
rs199569858 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107639380 | GAGAATAAAAAAAAA[-/A]GCCACAGATTAGGAG | 10451 |
rs199571589 | in-del | -/AAG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945836 | TCAAAAAAAAAAAAA[-/AAG]AAAGAAAGAAAAGAA | 10451 |
rs199629420 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107761218 | CATGGTGAAACCCCA[G/T]CTCTACTGAAAATAC | 10451 |
rs199647623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107727962 | GCAAGAAATTTAATT[A/G]AATTTCTAACTCACT | 10451 |
rs199663196 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796801 | TTGTAAAAAAAAAAA[-/T]AAAATATATATATAT | 10451 |
rs199668946 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107762116 | AACTATGGTGTTCTT[A/C]AAAAAAAAAAAAAAA | 10451 |
rs199669826 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107758406 | AGACCCCATCTCTAC[-/A]AAAAAAAAATTAAAA | 10451 |
rs199690057 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107943584 | CCATCTCTACTAAAA[A/G]TACAAAAATTAGCTG | 10451 |
rs199697526 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952466 | AACTTATAACAAAAC[-/T]TTTATATATATATAT | 10451 |
rs199698076 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107940017 | AGAGGCCAAGCAAGA[A/C]GATTTTGAAGTGATG | 10451 |
rs199711713 | in-del | -/TTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107645322 | ATATAATGGAATGTA[-/TTT]TTTTTTTTTTTGGTC | 10451 |
rs199724182 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107631154 | GTATTGTAACACCTA[-/T]TTTTTTTTGAGACAT | 10451 |
rs199726157 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107653867 | AACTGAAAAAATTGC[C/T]CCCTTCCCAGGAACA | 10451 |
rs199740870 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582840 | GGGTTGGTTCCAAGT[A/C]TTTGCTATTGTGAAT | 10451 |
rs199748018 | in-del | -/ATA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918703 | TATATATATATATAT[-/ATA]TTTTTTTTTTTTTTT | 10451 |
rs199752580 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107663500 | AAAATGAATATAATG[-/A]AAAAAAAAATGGTTT | 10451 |
rs199752582 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107609754 | ACCCCCCTCGCAGAT[A/G]AAGATATGGAAAGGT | 10451 |
rs199768177 | snp | A/G | 0.000165033 | 0.00908236 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642723 | GGGGTGGTGTTCCAG[A/G]ATAGTTCCTAATGAC | 10451 |
rs199774300 | snp | A/C | 4.48823e-05 | 0.004737 | intron-variant | VAV3 | GRCh38.p7 | 1:107760920 | TGTTAGGGAGTCATA[A/C]ACATTAAAAGATGCA | 10451 |
rs199797001 | in-del | -/CAAAA | 0.148326 | 0.228391 | intron-variant | VAV3 | GRCh38.p7 | 1:107598355 | AACGAAACTCTGTCT[-/CAAAA]CAAAACAAAACAAAA | 10451 |
rs199807202 | in-del | -/A | 0.368529 | 0.220116 | intron-variant | VAV3 | GRCh38.p7 | 1:107840922 | TTCAGAGATGCTTTT[-/A]AAAAAAAAAAAAATT | 10451 |
rs199808301 | in-del | -/ACA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107762136 | AAAAAAAAAAAAGGG[-/ACA]CCATACAAATATTAT | 10451 |
rs199812666 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107847450 | AGGAGATAGAGATAC[-/A]AAAAAACCCTTCAAA | 10451 |
rs199821366 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107882564 | TAAGGAGGAAGAGGT[A/G]TAAGGAATATAATAA | 10451 |
rs199842105 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774923 | ATTTGCTTTTTTTTT[G/T]TTTTTAAGATAACCC | 10451 |
rs199880370 | in-del | -/CTAACACCC | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107954462 | ATACCTGTCAAAAGT[-/CTAACACCC]ATTTTATACTGAATA | 10451 |
rs199919527 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893202 | TTAGTGACTTATTTT[C/T]CAGCAAGATTATATA | 10451 |
rs199922806 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922965 | TCAAAAAAAAAAAAG[A/G]AAAAAAAAAAAAAGA | 10451 |
rs199923569 | in-del | -/C | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107878128 | ATAGTGCCATATATG[-/C]TTTTGCACCTATACC | 10451 |
rs199928006 | in-del | -/A | 0.0777841 | 0.181223 | intron-variant | VAV3 | GRCh38.p7 | 1:107948841 | GAGAGACTCCATCTC[-/A]AAAAAAAAAATAAAC | 10451 |
rs199960276 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650861 | TGATGATTTCCAATC[A/T]CAATAGCAAAGACTT | 10451 |
rs199989395 | snp | C/T | 0.00120584 | 0.0245248 | intron-variant | VAV3 | GRCh38.p7 | 1:107772862 | CAACAAAGGATATCA[C/T]ATAAGGTCATTTTCT | 10451 |
rs199994097 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107750018 | GCCTTGAGAAGTGTT[C/G]ATCCCTTTCACAAAC | 10451 |
rs199997178 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107776875 | CACTTATCTCTCCCT[A/T]CCTTGAACTTATAAG | 10451 |
rs199998870 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107875489 | CGTAGCACACAACAG[C/T]CCAGACTAAAGAAGT | 10451 |
rs200015431 | in-del | -/AAG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107687030 | GCAATGAGAAAGTGA[-/AAG]AAGGCTGCTTTGCAA | 10451 |
rs200023828 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722840 | GCCCTATTATCCTCT[C/T]TTTTTTTTTTTTTTT | 10451 |
rs200029917 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732863 | GAAGAGAGCAGTGGT[A/T]CTCCCGGCATGGTGT | 10451 |
rs200042150 | in-del | -/A | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107936232 | ATTTGAATAATCAAC[-/A]ATGACTTAATGCAAC | 10451 |
rs200042921 | in-del | -/AGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107573854 | ATTTATGTCACTATC[-/AGT]ATATTCATTTCAAAT | 10451 |
rs200046624 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889535 | ATGGTCTTCCTACAG[-/A]AAAAAAAAAACTGGT | 10451 |
rs200046955 | in-del | -/T | 0.0333695 | 0.124785 | intron-variant | VAV3 | GRCh38.p7 | 1:107833556 | ACAAAATTTTAGAAA[-/T]TTTTTTTTCTAATTT | 10451 |
rs200060988 | in-del | -/T | 0.0283406 | 0.115616 | intron-variant | VAV3 | GRCh38.p7 | 1:107651505 | TCAATTATTTATTTA[-/T]TTTTTTTTCAAAAAG | 10451 |
rs200066845 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822667 | CAAAAAAAATAAATA[A/T]ATAAATAAATAAATA | 10451 |
rs200076516 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107617579 | TACACATGGGCAAGG[C/T]TTGACTGCATCACTT | 10451 |
rs200091205 | in-del | -/TTATTA | 0.499325 | 0.0183582 | intron-variant | VAV3 | GRCh38.p7 | 1:107884406 | TTAAAAATAAATTAT[-/TTATTA]TTATTATTATTATTA | 10451 |
rs200099223 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107800179 | AGATACCTCTTCAAT[A/G]TATTTATTTCCACTA | 10451 |
rs200099364 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732951 | CCTAACTGGGAGACA[A/T]CTCCTAGTAGGGGCT | 10451 |
rs200120013 | snp | C/T | 0.000249155 | 0.0111586 | intron-variant | VAV3 | GRCh38.p7 | 1:107596162 | TTTAATGTTATTGTG[C/T]CCCTAATTTTTAAGT | 10451 |
rs200129742 | in-del | -/AGGG | 0.26271 | 0.249677 | intron-variant | VAV3 | GRCh38.p7 | 1:107651542 | GAAACAAAGTAAGGA[-/AGGG]AGGGAGGGAGGGAGG | 10451 |
rs200132696 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107630348 | GGAAGAATGGATGGG[A/T]GGATGGATGGATGGA | 10451 |
rs200141143 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625271 | TTTTTTTTTTTTTTT[C/T]TTTTTGGGACGGCAT | 10451 |
rs200163484 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107885258 | GTCTGTCGCTTTTAT[C/T]TTTTATTTTTATTTT | 10451 |
rs200164437 | snp | A/C | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874905 | AGTATAATTACCTTT[A/C]CAAAGTCACGAACAT | 10451 |
rs200175624 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107606959 | GGTAGGAGTCTGATC[A/T]TTTTTTTTTTTTTAA | 10451 |
rs200179204 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107948852 | ATCTCAAAAAAAAAA[C/T]AAACAAACAAACAAA | 10451 |
rs200181110 | snp | A/C/G | 0.000116238 | 0.00762279 | missense, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749564 | TTTTCTCTTACATAC[A/C/G]ATCACTGCCAAATCA | 10451 |
rs200212088 | in-del | -/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107912073 | TTGTGTGTGTGTGTG[-/TG]CGTGTTTACGTTAGT | 10451 |
rs200212485 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722856 | TTTTTTTTTTTTTTT[A/C]TACGCTTACTAAGTA | 10451 |
rs200230420 | in-del | -/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107754984 | AACTCTTTTTTTTTT[-/T]AAACTGTCTCCTCAA | 10451 |
rs200239934 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107842545 | TTCACTTTAATCTTT[A/C]GCATCTCTTTTCTCT | 10451 |
rs200240599 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107825970 | CCTGGAGGAAAGGAA[A/T]CATTTCTTATAATCC | 10451 |
rs200243331 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575018 | GCGCGCGCGCGCGCA[C/T]ACGCGCGCGTGTTTA | 10451 |
rs200246526 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724891 | AATGCCATTTGTGCA[C/T]ATACTCCAGAAATCT | 10451 |
rs200261032 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107683596 | TTGCACTATTAAATT[G/T]TATTACTACTGGCAC | 10451 |
rs200266673 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925892 | CATATAAATATATAA[C/T]ATATATGATATATAT | 10451 |
rs200270148 | snp | A/C | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966507 | CTCTGTCTCAAAAAA[A/C]AAACAAACAAACAAA | 10451 |
rs200285752 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107913695 | CTGTCAATACAGTTA[A/T]GCACCAACCTATACA | 10451 |
rs200287415 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107851889 | TTACGAGTTTGCTGA[-/T]TTTTTTTAAAAAAGT | 10451 |
rs200312853 | snp | C/T | 0.00199808 | 0.0315444 | missense, intron-variant, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107688391 | CTTACCTCTGGTAGT[C/T]TGAGTGTCCCTTGTT | 10451 |
rs200322314 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107579926 | TCCTTCCCCGACCTC[C/T]GCTGACCTTAACTTC | 10451 |
rs200322757 | in-del | -/GCAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107634594 | AAACACCAAAAGCAA[-/GCAA]TGGCAATGAAAGCCA | 10451 |
rs200329382 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107848288 | ACTGCACTCCAACCT[G/T]GGCAACAGAGCAAGA | 10451 |
rs200357683 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107804768 | ATTTTTGGTTTTTTT[-/A]TGTTTGTTTGTTTTG | 10451 |
rs200365018 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107626019 | CCCTTACCCTGCAGG[-/A]AAAAAAAAAGAGATA | 10451 |
rs200365455 | in-del | -/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107578487 | ACACACATCTAACTC[-/T]TATTATTGGCAGAAA | 10451 |
rs200373376 | in-del | -/TTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107586140 | ACTCCCTTGGCATAG[-/TTT]TTTTTTTTTTTTTTT | 10451 |
rs200394113 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107859489 | TCGATGACTGATTTA[C/G]TGCTTAGCTGATAAT | 10451 |
rs200408211 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107729462 | AGAAAACCTGAGTTT[-/A]AAAAAAAAACATGAG | 10451 |
rs200424694 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107623488 | GTAAACTTGCTAAGC[C/T]GCAAGGAACATAGAC | 10451 |
rs200438570 | in-del | -/TATTA | 0.0663309 | 0.169604 | intron-variant | VAV3 | GRCh38.p7 | 1:107858365 | TTTTGAAATTTTAAC[-/TATTA]TATTTCTTAGAACCA | 10451 |
rs200446495 | in-del | -/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595426 | TCTAGATATCCCAGT[-/G]TTGCTTAGGCTAAAG | 10451 |
rs200453194 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107710036 | TAATAATACATATGA[-/T]TTTTAAAACATACAT | 10451 |
rs200461998 | in-del | -/T/TAT | 0.346368 | 0.23068 | intron-variant | VAV3 | GRCh38.p7 | 1:107796802 | TGTAAAAAAAAAAAA[-/T/TAT]AAATATATATATATA | 10451 |
rs200480971 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107766560 | AAGTTCCTAAGAAAA[-/G]AAAACAATGTGAAAG | 10451 |
rs200482864 | in-del | -/C | 0.0209421 | 0.100162 | intron-variant | VAV3 | GRCh38.p7 | 1:107770282 | AATGCCACCAGCCCT[-/C]CCCCCCCCATCACTC | 10451 |
rs200491565 | snp | A/G | 0.000344268 | 0.0131155 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755397 | TGATGTGGGGGTGAG[A/G]GGAAGCTGGATGGAA | 10451 |
rs200513412 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107738565 | TGTCTACTGCCCCAT[A/G]AAGACAAAAAACTAA | 10451 |
rs200516457 | snp | A/G | 5.21889e-05 | 0.00510801 | intron-variant | VAV3 | GRCh38.p7 | 1:107760745 | ATATTTTGTTGAGTG[A/G]ATAAATGGACAATAA | 10451 |
rs200526746 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107804977 | TTGGGTTTTTTTTTT[-/G]ATTCCCCTGGCAGCA | 10451 |
rs200561012 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693981 | TAGAACCCATGTGTC[-/A]AAGCTGGCAAAGTCA | 10451 |
rs200569502 | in-del | -/CC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726382 | TCCGGCAGAGGCGCT[-/CC]CTGCAGATACTTTTC | 10451 |
rs200571938 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107841292 | TATTTAGGGGAAAGG[A/G]GGGGGTAGAAAAAGA | 10451 |
rs200590891 | in-del | -/A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107762133 | AAAAAAAAAAAAAAA[-/A/G]GGGCCATACAAATAT | 10451 |
rs200596420 | in-del | -/A | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107681242 | AATTAACTGTAGGAT[-/A]AAAAAAAAATCAAAG | 10451 |
rs200623953 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892617 | CCAAAAAATTAGTTA[A/C]AAAAAAAAATGATGT | 10451 |
rs200624655 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933282 | TGTGGTGGTTTTTTT[G/T]TGTTTTTTTTTTTCC | 10451 |
rs200639702 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893055 | AGAATTAAAAATATA[A/C]ACAGAGTAAAAAACT | 10451 |
rs200650424 | in-del | -/G | 0.0733688 | 0.176922 | intron-variant | VAV3 | GRCh38.p7 | 1:107849636 | CTAGTAGAAAACCTA[-/G]GCAATACCACTCAGG | 10451 |
rs200651979 | in-del | -/G | 0.0119091 | 0.0762411 | intron-variant | VAV3 | GRCh38.p7 | 1:107779181 | TTAAAAAAAAAAAAA[-/G]AAGAAGAACCACACC | 10451 |
rs200666582 | in-del | -/T | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107882534 | GGTCTCAGATCATCC[-/T]TTTTTTTTAACTGGT | 10451 |
rs200668238 | in-del | -/AAAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822655 | AGACTCCATCTCAAA[-/AAAT]AAAAATAAATAAATA | 10451 |
rs200668570 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822669 | AAAAAAATAAATAAA[A/T]AAATAAATAAATAAA | 10451 |
rs200669581 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107749438 | TTATAAGTAAATTAC[A/T]GTTATTAGTTTCCAA | 10451 |
rs200676718 | snp | C/T | 1.65023e-05 | 0.00287244 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107770690 | TGTCTGCTTAATTTC[C/T]GCTAGACAACAACTT | 10451 |
rs200711762 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107924392 | CAGTCGATATTATGA[A/C]AAAAAAAAAAAAAAC | 10451 |
rs200714141 | in-del | -/AATC | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107726492 | GTCATTGATTAAATT[-/AATC]AATCAATTATCTACA | 10451 |
rs200722364 | in-del | -/AATAC | 0.0205511 | 0.0992634 | intron-variant | VAV3 | GRCh38.p7 | 1:107878074 | AACAAAAGTTGAAAG[-/AATAC]AATGAACATTCCATC | 10451 |
rs200729870 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711922 | AACTCCTGACCTCAG[A/G]TGATCTGCCCACCTC | 10451 |
rs200730509 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107715221 | AGAACCTGTTCCACC[A/G]AGCACTCAAATTTGT | 10451 |
rs200740159 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107620003 | CCAGATTGAATCCCA[G/T]GCACACCTTTCCATA | 10451 |
rs200765188 | snp | A/G | 0.000471968 | 0.0153545 | intron-variant | VAV3 | GRCh38.p7 | 1:107704685 | AGTGGTATATTAAAC[A/G]GTGCAAAATTCTGCC | 10451 |
rs200766411 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107912346 | AAATGCATAAGAAAA[C/T]ACCACCAAGGGCAGA | 10451 |
rs200772253 | in-del | -/AT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107919615 | AGGATAGAGAGGGGA[-/AT]ATATATATATTATGC | 10451 |
rs200777541 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107646830 | AAATAAAACTAAAGC[C/T]ACATGTAGGTATGCA | 10451 |
rs200778284 | snp | A/G | 0.000379047 | 0.0137615 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574167 | GAAGTCATACCGAGC[A/G]ATGGCAATGCCCAGC | 10451 |
rs200786279 | in-del | -/T | 0.399073 | 0.200692 | intron-variant | VAV3 | GRCh38.p7 | 1:107802883 | GTTTTTTTTTTTTTT[-/T]GAAGAGTTAGAGTTG | 10451 |
rs200786445 | in-del | -/TGTGTG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624375 | TTATAGTCTTATGAC[-/TGTGTG]TGTGTGTGTGTGTGT | 10451 |
rs200803370 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925917 | ATATATGTTACATAT[A/G]TAACATACGTATATA | 10451 |
rs200816784 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107874730 | GTGTGGGGTTTCTTT[G/T]TTGTTGTTGTTTTTT | 10451 |
rs200816959 | in-del | -/CTGGTG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107806421 | AGTTCTGGGATATTG[-/CTGGTG]TTAGTCTTGCTGCTG | 10451 |
rs200817313 | in-del | -/A/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950139 | CAAAACAAAAAAAAA[-/A/AA]GTACTTCTACTGTAT | 10451 |
rs200821750 | in-del | -/TTAG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107962329 | GAGATGAGTAGTTAG[-/TTAG]CGGCAAAATGTCTAG | 10451 |
rs200824303 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107608162 | ATATTATTCTAACTG[G/T]TCATATTTTCAGTAG | 10451 |
rs200828500 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107634713 | GGAGAAAATTTTTGC[A/G]ATCTACTCATCTGAC | 10451 |
rs200829526 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107735208 | GACACATTTAAAGCA[G/T]TGTGTAGAGGGAAAT | 10451 |
rs200837698 | in-del | -/A | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107893575 | TGGATGGCAGCAGGC[-/A]AAAAAAAGCTTCCGG | 10451 |
rs200845787 | in-del | -/TCTC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107574959 | GTTCAGAGTTGAGTT[-/TCTC]TCTCTGTGTGTGTGT | 10451 |
rs200866762 | in-del | -/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107665180 | GAACAATTGGGAGAC[-/TA]TTACAACAGCTGACA | 10451 |
rs200871490 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107902070 | CAAAAAAAACAACAA[A/C/T]AAAAACTGTTATTGT | 10451 |
rs200876765 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809270 | GCACTATAATTAGAC[-/T]ACAACCTAAGAGTCT | 10451 |
rs200885478 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107644946 | CACTAGTATACTCTG[G/T]ATACTCGAGTATACA | 10451 |
rs200898294 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575028 | GCGCACACGCGCGCG[C/T]GTTTAATATTCGATG | 10451 |
rs200917340 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107900790 | GGGACTTTGTGGTCT[C/G]TGAACTTAACAGACA | 10451 |
rs200941675 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922966 | CAAAAAAAAAAAAGA[A/G]AAAAAAAAAAAAGAG | 10451 |
rs200951858 | in-del | -/CCAG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107943625 | CACACACCTGTAGTC[-/CCAG]CTACTCGAGAGGCTG | 10451 |
rs200980013 | snp | A/G | 0.000269892 | 0.0116135 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107779443 | GCTTACCTGATTCCT[A/G]TGGCCAATGCTATAG | 10451 |
rs200982342 | in-del | -/A | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107855928 | TCCACTTCTACCCAG[-/A]AAACAGTGCAGTGCT | 10451 |
rs200982477 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582956 | CTGGGTCAAATGGTA[A/T]TTCTAGTTCTAGATC | 10451 |
rs200993370 | in-del | -/CT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107626963 | AAAATTCTACTGGAG[-/CT]AATATTGTTGTGTGG | 10451 |
rs200994829 | in-del | -/AAAT | 0.0364509 | 0.129988 | intron-variant | VAV3 | GRCh38.p7 | 1:107822658 | ACTCCATCTCAAAAA[-/AAAT]AAATAAATAAATAAA | 10451 |
rs201003847 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903165 | TAGCAGGATATTTAA[-/T]TTTTTTAAAAAAATC | 10451 |
rs201005615 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107770223 | AGTTCACTTAGCTGC[A/C]CACTTAATCTTGTCA | 10451 |
rs201011870 | in-del | -/A | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107857782 | ATTGTCAACTTTACC[-/A]AAAGACTTTGCTGGG | 10451 |
rs201014454 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107763721 | AAGCAAAAAGATCAC[A/G]TATCTAGTACAGTTA | 10451 |
rs201018621 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650852 | TACTGAGAATGATGA[C/T]TTCCAATCACAATAG | 10451 |
rs201019196 | in-del | -/C | 0.0252325 | 0.109451 | intron-variant | VAV3 | GRCh38.p7 | 1:107804499 | ACTTATCACAGATCA[-/C]CCCCAAAAAAGAAAC | 10451 |
rs201023623 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107686701 | TATTGAAGAGTGAAA[C/G]AAGTCACTAAAAAAC | 10451 |
rs201042340 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732899 | CTCTGAGAATGGACA[G/T]ACTGCCTCCTCAAGT | 10451 |
rs201046943 | in-del | -/GTATATGTATATGTATATGTATAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728601 | TATGTATACGTATAC[-/GTATATGTATATGTATATGTATAT]GTATATGTATATGTA | 10451 |
rs201059174 | in-del | -/TAT | 0.433527 | 0.169758 | intron-variant | VAV3 | GRCh38.p7 | 1:107918704 | ATATATATATATATA[-/TAT]TTTTTTTTTTTTTTG | 10451 |
rs201078360 | in-del | -/TTGAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814506 | TTACTTACTGTTGAG[-/TTGAT]TTCCCAGTATATTCT | 10451 |
rs201088965 | in-del | -/C | 0.0240643 | 0.107019 | intron-variant | VAV3 | GRCh38.p7 | 1:107879337 | GCTTAAGCAATCTAT[-/C]ACTTGCAACAGAACG | 10451 |
rs201089551 | in-del | -/C | 0.0418186 | 0.138422 | intron-variant | VAV3 | GRCh38.p7 | 1:107732388 | TGCGGCCACAGAGGG[-/C]GAGCCAAAGCTGGGC | 10451 |
rs201116818 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107796800 | ATTTGTAAAAAAAAA[A/T]AAAAATATATATATA | 10451 |
rs201154213 | in-del | -/TATAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918702 | ATATATATATATATA[-/TATAT]TTTTTTTTTTTTTTG | 10451 |
rs201167785 | in-del | -/CAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957306 | CTCTATCCCTCTATT[-/CAC]CTCCTTTCTCTGGCC | 10451 |
rs201181193 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928936 | GATTTAACCCAAAGA[A/C]GACTACCTCAAGGTA | 10451 |
rs201182307 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107885260 | CTGTCGCTTTTATTT[C/T]TTATTTTTATTTTTT | 10451 |
rs201207716 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107829838 | CAGATTTGCTCCATA[G/T]CATTTAATCAGAACA | 10451 |
rs201215793 | snp | A/G | 0.00199792 | 0.0315431 | intron-variant | VAV3 | GRCh38.p7 | 1:107875020 | TCAAACAGAGAAACT[A/G]AGGAATGGAAAAGAG | 10451 |
rs201216447 | in-del | -/G | 0.0252325 | 0.109451 | intron-variant | VAV3 | GRCh38.p7 | 1:107918807 | GCCTCCCGAGTTCAA[-/G]CAATTCTCTTGCCTC | 10451 |
rs201222965 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107874747 | TGTTGTTGTTTTTTG[A/C]TTTTTGGTTTTGCTA | 10451 |
rs201226865 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107608066 | AAAAAAAGAAAAGTA[A/T]TTTAAAATTCTACTA | 10451 |
rs201263900 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107843551 | TGTATATATATATAT[A/T]TATATATATATATAT | 10451 |
rs201264026 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774912 | AGGGATAATACATTT[G/T]CTTTTTTTTTTTTTT | 10451 |
rs201277774 | snp | A/G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724892 | ATGCCATTTGTGCAT[A/G/T]TACTCCAGAAATCTG | 10451 |
rs201294174 | in-del | -/A | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107922452 | TGACTTTCACTTTTT[-/A]AAAGTTTTATATGAA | 10451 |
rs201306494 | snp | C/T | 1.65051e-05 | 0.00287267 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107777284 | ATTAATGCTTTCTTC[C/T]GTTGGGAAGGGCCTA | 10451 |
rs201310673 | in-del | -/TT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107912058 | TTTTTTGTTTGTTTG[-/TT]TGTGTGTGTGTGTGC | 10451 |
rs201320589 | in-del | -/G | 0.0197687 | 0.0974348 | intron-variant | VAV3 | GRCh38.p7 | 1:107628092 | AGAAAAGGCAACCCA[-/G]TATTGTGCCTTGATG | 10451 |
rs201322360 | in-del | -/CAG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796993 | TAAATAAGTGAAAAT[-/CAG]ACTCCTATAATAACT | 10451 |
rs201323375 | in-del | -/CTACTG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772910 | ATAGCTACAAATAGC[-/CTACTG]GATTTTAGTAAAAAA | 10451 |
rs201327774 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107623754 | AACAAAACCATAAGC[C/T]ATGCATTTTTGTTAT | 10451 |
rs201349042 | in-del | -/T | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107585360 | CATCTATTTTCATGG[-/T]TTTTTTTTATTATAA | 10451 |
rs201380058 | snp | A/T | 1.65021e-05 | 0.00287241 | intron-variant | VAV3 | GRCh38.p7 | 1:107683463 | GCTGAAGCCATAATT[A/T]TGGAAGGTTTAATCA | 10451 |
rs201400164 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624445 | TACCTTTAATGATAG[A/G]AAAAAAAAATTTGGC | 10451 |
rs201406581 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107652373 | ACAAAAATGGCCAAT[C/G]AACAGTCCCTGGGGC | 10451 |
rs201411038 | in-del | -/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757118 | TATTTTATTTATGTG[-/TA]TATATATATGTTTGT | 10451 |
rs201411686 | snp | A/C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107784063 | AGACCCTATCTCAAA[A/C/T]ATATATATATATATA | 10451 |
rs201422146 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107887365 | AATATCAATAATACT[C/T]TCATAAATAAATGTA | 10451 |
rs201428398 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582964 | AATGGTATTTCTAGT[C/T]CTAGATCCCTGAGGA | 10451 |
rs201435660 | snp | A/G | 0.000900225 | 0.0211967 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964722 | TGGAGTGCGCCCGGA[A/G]GTTGTTAAGCAGCTG | 10451 |
rs201450388 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107891150 | AGTGTCCCTTTCTTT[-/A]AAAAAAAAAAAAATC | 10451 |
rs201457734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761112 | ATTATTTTCTTGGCC[A/G]GGCGCGGTGGCTCAC | 10451 |
rs201479436 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107851191 | AAAAAAAAAAAAAAA[C/T]AAGCCGGCCCTCATT | 10451 |
rs201491269 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107700276 | CATGAGCAATAAGCA[A/T]TTTTTAAAGTTTTAT | 10451 |
rs201492244 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893057 | AATTAAAAATATACA[C/T]AGAGTAAAAAACTTG | 10451 |
rs201506627 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107960476 | TCTCAAAAAAAAAAA[-/A]GAAAAGAAAAGAAAG | 10451 |
rs201509460 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107958634 | TTTTACTTATTTTTT[-/C]TTTATCATTATACTT | 10451 |
rs201515652 | snp | A/G | 0.00102688 | 0.0226359 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107765163 | ACTGCAGTACTGCCC[A/G]TAAATAACCAATCTG | 10451 |
rs201526731 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107899284 | TAGAGATATATTAAT[-/A]AAAAAAATGTCTGGG | 10451 |
rs201574180 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | VAV3 | GRCh38.p7 | 1:107583726 | CCTCTTCAAGGAGAA[C/T]TACAAACCACTGCTC | 10451 |
rs201579552 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107598824 | CACACACACACACAC[A/G]TATACATAATGTCAC | 10451 |
rs201582671 | in-del | -/AAC | 0.0433465 | 0.140692 | intron-variant | VAV3 | GRCh38.p7 | 1:107724102 | ATGTGAGTCATGAAG[-/AAC]AACAGCAACATTTTA | 10451 |
rs201592793 | in-del | -/T | 0.0267878 | 0.112589 | intron-variant | VAV3 | GRCh38.p7 | 1:107837353 | GACACAGAAAAAAAC[-/T]TTGAATAAAATCTAA | 10451 |
rs201592799 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107843553 | TATATATATATATTT[A/T]TATATATATATATGA | 10451 |
rs201623100 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621246 | ATGGTCATAGGCATT[-/C]CTGTAGATGACAGAG | 10451 |
rs201629004 | in-del | -/TAAG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107712737 | GATGATGAACAAAAA[-/TAAG]TAAAGTCCCTGACTA | 10451 |
rs201642241 | in-del | -/TG | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786987 | ACCTATCTACACACA[-/TG]CACATACACACATAC | 10451 |
rs201642537 | in-del | -/A/AC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107611608 | ACCAAAAAAAAAAAA[-/A/AC]CAAACAAACAAACAA | 10451 |
rs201652526 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107885256 | AAGTCTGTCGCTTTT[A/T]TTTTTTATTTTTATT | 10451 |
rs201661016 | snp | C/T | 0.000230225 | 0.0107266 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107766531 | TCTTGCATTAGGTTC[C/T]GATGAAGTTTTACAA | 10451 |
rs201680043 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107920408 | CCCCTAAATGATGAG[A/G]CTAAAACCAAACCAA | 10451 |
rs201685860 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107670480 | TGAAGATTAAACATA[-/T]TTTTTTTTTTGCCTT | 10451 |
rs201699562 | snp | C/T | 0.00035175 | 0.0132571 | intron-variant | VAV3 | GRCh38.p7 | 1:107642573 | CAAGATTTAAGAACC[C/T]TCTCTTGGGGTCTGC | 10451 |
rs201705921 | in-del | -/A | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107849243 | ATTTCATATGCAACC[-/A]AAAAAAAAAAAAAGT | 10451 |
rs201724164 | snp | C/T | 3.33756e-05 | 0.00408493 | intron-variant | VAV3 | GRCh38.p7 | 1:107749622 | GATTGATTGATTGAT[C/T]TTAAATGGTTTAGAA | 10451 |
rs201728432 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896386 | CCTCTTTCATCAAAT[C/T]AATCGCACAGCAGCC | 10451 |
rs201731204 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947398 | TAGAGTTCTAAGAGT[C/T]CCAAAAGAACTGTGA | 10451 |
rs201733308 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959032 | TTCGGGAGGCCAAGG[C/T]GGCCTGATGACCTGA | 10451 |
rs201735108 | snp | G/T | 0.000235239 | 0.0108427 | intron-variant | VAV3 | GRCh38.p7 | 1:107768551 | AATTAAGTATAACTT[G/T]TCCTAATCTATATAA | 10451 |
rs201787495 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575017 | CGCGCGCGCGCGCGC[A/G]CACGCGCGCGTGTTT | 10451 |
rs201801980 | in-del | -/ACTGG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772912 | AGCTACAAATAGCCT[-/ACTGG]ATTTTAGTAAAAAAT | 10451 |
rs201806785 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732857 | AGCTCTGAAGAGAGC[A/C]GTGGTTCTCCCGGCA | 10451 |
rs201809847 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757155 | TATATGTGTGTATAT[A/G]TGTGTGTGTGTGTGT | 10451 |
rs201820314 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736693 | CAAACCACTGCTCAA[C/T]GAAATAAAAGAAGAC | 10451 |
rs201822046 | in-del | -/A | 0.0256215 | 0.110247 | intron-variant | VAV3 | GRCh38.p7 | 1:107686401 | AGAAAGAAGGTCTTC[-/A]AGAGAGGAGAAAAAA | 10451 |
rs201825987 | snp | C/T | 0.000465302 | 0.0152458 | intron-variant | VAV3 | GRCh38.p7 | 1:107875067 | AATTATTCTGAATGC[C/T]ATCCACCCTCTGTAA | 10451 |
rs201826370 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107836195 | CCTAATAGACATTGA[C/T]AGAATACTCAACCCA | 10451 |
rs201830011 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736979 | GCTACAGTAACCAAA[A/C]CAGCATGGTACTGGT | 10451 |
rs201833901 | snp | A/G | 0.026212 | 0.11144 | intron-variant | VAV3 | GRCh38.p7 | 1:107617639 | ATTTCTGCCCTAAGG[A/G]AAAAAAAAAAATGCC | 10451 |
rs201836582 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621089 | ATCATATCAAAACTC[A/T]TTTTTTTTTTTTTAC | 10451 |
rs201836900 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107779660 | GAAGTATAAACACCT[A/G]GATTATAATTTTATA | 10451 |
rs201854606 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650857 | AGAATGATGATTTCC[A/G]ATCACAATAGCAAAG | 10451 |
rs201875355 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107670870 | TTCCTGTTTTGCTAG[-/A]AAAAAAAAATCCTTG | 10451 |
rs201878985 | snp | C/G | 1.654e-05 | 0.00287571 | intron-variant | VAV3 | GRCh38.p7 | 1:107772868 | AGGATATCATATAAG[C/G]TCATTTTCTATTATG | 10451 |
rs201883150 | in-del | -/TGAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107859478 | TGGAATAATTCTCGA[-/TGAC]TGATTTAGTGCTTAG | 10451 |
rs201885990 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107909615 | TAAAATGGGAAATTT[C/T]CGAAAAACTTATGGT | 10451 |
rs201896239 | in-del | -/AAAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822658 | ACTCCATCTCAAAAA[-/AAAT]AAATAAATAAATAAA | 10451 |
rs201915427 | in-del | -/TAAAT | 0.0182019 | 0.0936463 | intron-variant | VAV3 | GRCh38.p7 | 1:107667648 | AACAATCATCCTCTA[-/TAAAT]TATTTAAAATAGCAA | 10451 |
rs201933161 | in-del | -/CTGGTC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107608159 | ATAATATTATTCTAA[-/CTGGTC]ATATTTTCAGTAGGA | 10451 |
rs201937231 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772916 | ACAAATAGCCTACTG[G/T]ATTTTAGTAAAAAAT | 10451 |
rs201951607 | in-del | -/A | 0.0275645 | 0.114116 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786319 | ACAAGAACTTCCTTT[-/A]AAAAAAAAAGCCATA | 10451 |
rs201979532 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107906257 | AGGCTTGTTTTGTTT[C/T]GTTTTGTTTTGTTTT | 10451 |
rs201989538 | snp | G/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595052 | AGAAAACTTCCATTT[G/T]TGAATGAGCAAAAAT | 10451 |
rs202001666 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107636475 | ATATTGAAAATATCA[C/T]AAGTCAAAAATGCAT | 10451 |
rs202047220 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796803 | GTAAAAAAAAAAAAA[-/T]AATATATATATATAT | 10451 |
rs202052672 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724836 | TGGATGTGGTGGGGG[A/G]AAAAAAAAAAGGCTA | 10451 |
rs202055489 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107820770 | CATAAAAATTAAAAA[C/T]TAGGAAAAAACTGAC | 10451 |
rs202059103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107775060 | CCTGCAAATACATTC[A/G]GACCTTCGGCCACCA | 10451 |
rs202063588 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925890 | CACATATAAATATAT[A/G]ACATATATGATATAT | 10451 |
rs202064472 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866849 | AAAAAAAAAAAAAAA[A/T]AGGGCATTTGTAACC | 10451 |
rs202065161 | snp | A/C | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896708 | TTTAAAAAGACTGGC[A/C]ATTTTGTTATTAATC | 10451 |
rs202066700 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107719586 | GAGTATGTGGAGAAA[C/T]AGGAACACTTTTACA | 10451 |
rs202070300 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107630347 | TGGAAGAATGGATGG[A/G]AGGATGGATGGATGG | 10451 |
rs202073666 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625270 | TTTTTTTTTTTTTTT[C/T]CTTTTTGGGACGGCA | 10451 |
rs202099611 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107850720 | GAACTTAAAGTATAA[-/T]TTTTTTAAAAAAAAG | 10451 |
rs202127664 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107600632 | GGCTCTCTGGCACAA[-/T]TTTTTTTTTAATGCT | 10451 |
rs202139989 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732925 | CAAGTGGGTCCCTGA[A/C]CCCCATGTAGCCTAA | 10451 |
rs202142490 | in-del | -/AAGC | 0.322721 | 0.23919 | intron-variant | VAV3 | GRCh38.p7 | 1:107634588 | TGTCTAAAACACCAA[-/AAGC]AAGCAATGGCAATGA | 10451 |
rs202147313 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950129 | TCTGGAAACCACAAA[A/C]CAAAAAAAAAGTACT | 10451 |
rs202158637 | snp | A/C/T | 0.000195912 | 0.00989547 | intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964640 | GCTGCCGGCTGGAGG[A/C/T]GGGGCGCCCGTGCCG | 10451 |
rs202170050 | in-del | -/TCTC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907701 | CGCTCTCTCTCTCTC[-/TCTC]ATTCTTACTCTCTTG | 10451 |
rs202173550 | snp | C/T | 0.000724798 | 0.019023 | intron-variant | VAV3 | GRCh38.p7 | 1:107757223 | GTCTTTAGGCAAGAA[C/T]AAAAAATACAAACAA | 10451 |
rs202197676 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940996 | ATTTTAGCACAATTG[A/G]AAAAAAAAAACCCTC | 10451 |
rs202231739 | in-del | -/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796409 | TTAGGGATCAGTTCT[-/TA]CTTAGAAAAAACAAG | 10451 |
rs202234684 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923563 | CAGTTCTGCATGGCT[G/T]AGGAGGCCTCAGGAA | 10451 |
rs202237918 | snp | G/T | 5.76341e-05 | 0.00536784 | intron-variant | VAV3 | GRCh38.p7 | 1:107688349 | ACTTGAAATGCAAAG[G/T]TTATAAAAAATATTT | 10451 |
rs202238122 | in-del | -/A | 0.0240643 | 0.107019 | intron-variant | VAV3 | GRCh38.p7 | 1:107955998 | ACATCAAATGAAGGG[-/A]ACAACGGCATACATG | 10451 |
rs367543372 | snp | C/T | 0.000149451 | 0.00864309 | missense, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749563 | CTTTTCTCTTACATA[C/T]GATCACTGCCAAATC | 10451 |
rs367555722 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107719854 | GAAAATGTGGCACAT[A/G]TACACCATGGAATAC | 10451 |
rs367585080 | in-del | -/AG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945837 | CAAAAAAAAAAAAAA[-/AG]AAAGAAAGAAAAGAA | 10451 |
rs367585610 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662125 | ATTTAAAGAGGCTGT[A/G]TTATTTTTAAAAAAT | 10451 |
rs367591543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594210 | ACCACTCTATATAAA[A/G]ATATGAAACTCCTCC | 10451 |
rs367596119 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | VAV3 | GRCh38.p7 | 1:107636806 | TGAAAATGAAAATAA[A/G]CAGCTTTGCAAAATT | 10451 |
rs367610433 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107609550 | TAAAACTATAAAAAA[A/T]AAAAAAAAAAACTAC | 10451 |
rs367620458 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809898 | TAAGGATCTCAATTT[C/T]CTAGAGAAACGTTGC | 10451 |
rs367629706 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681896 | CCATCTCCTGACCTC[A/G]TGATCCGCCGGCCTT | 10451 |
rs367635696 | in-del | -/TTGTT/TTGTTTTGTT | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107906245 | ACCCTAAGCCAAGGC[-/TTGTT/TTGTTTTGTT]TTGTTTTGTTTTGTT | 10451 |
rs367636761 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107827147 | CTGAACTACCTATGA[C/T]GACATTCAGTCAAGG | 10451 |
rs367642843 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107802805 | TGTAGTCTACTTTCT[A/G]TTGTGTGCTTGTCTG | 10451 |
rs367666086 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107937088 | ACATAACACCCTCCA[A/C]CGCCACCCCAAAAAA | 10451 |
rs367681144 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107914386 | GTCTCTCCTGTGGCA[C/G]GGCACTAGAGTCACA | 10451 |
rs367684095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891764 | GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGC | 10451 |
rs367693378 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107877192 | AAAATTCATAAGAGA[A/C]CTTTAAGACACAGAA | 10451 |
rs367693926 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952284 | TGGGCACACGGAGGG[G/T]AACCACACACACTGG | 10451 |
rs367698311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594703 | ACTTCATTCATTGCC[A/G]GGCTACATTCTCTGA | 10451 |
rs367698924 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107904959 | CATTTAAGCAAATGC[C/T]TGAAGTAAATAGGAA | 10451 |
rs367729069 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658096 | AAGAAAACCGTACTT[C/T]CTTTCAAATTAATGG | 10451 |
rs367750056 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107752068 | AAGCTGGAAGTCTCA[C/T]ACTTACTGACTTGTT | 10451 |
rs367756427 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107674995 | AAGGAATGGAATCCC[A/G]CGAAAAGCAGTGTAA | 10451 |
rs367768448 | snp | A/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589824 | GTTAGGAACCTGTAC[A/G]AAGGAGATAATAAAT | 10451 |
rs367771504 | snp | C/T | 4.10248e-05 | 0.00452888 | intron-variant | VAV3 | GRCh38.p7 | 1:107749082 | CCATAAGACCACTGT[C/T]AAAATTAATATTCCT | 10451 |
rs367779362 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107761142 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 10451 |
rs367824746 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814650 | AATCCCATTTTTCTA[C/G]TTTTGATTTGTTGCC | 10451 |
rs367826270 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107684276 | AGTAATCTCACTAAT[G/T]AAGAAGGGCTTGATT | 10451 |
rs367827223 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107659434 | TACTTACATTTCTAC[A/G]AATCCTATAGACTTC | 10451 |
rs367827767 | snp | A/G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701826 | AAGTTCCTCATCTCC[A/G/T]TTTGGGACCACCTCA | 10451 |
rs367830082 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723060 | CTTCGTCATGTTATT[G/T]TGTAATTATTTGTAA | 10451 |
rs367831375 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107716629 | TGTGCTGCTGGATTC[A/G]GTTTGCCAGTATTTT | 10451 |
rs367838482 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107745926 | CTCAAGGGACTCGTG[G/T]TGATACTAAAGACAC | 10451 |
rs367840644 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107770288 | CACCAGCCCTCCCCC[A/C/G]CCATCACTCTCTATC | 10451 |
rs367843777 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753812 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 10451 |
rs367856281 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107905552 | AAAAAAATCTAGAAT[A/T]CTTTTTATGAATGAA | 10451 |
rs367856477 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866810 | CCTGGGCAAAAGAGC[A/G]AGACTCCATCTCAAA | 10451 |
rs367863610 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107928786 | AAAGGGAAACCTAAG[A/C]GTTATTGGCCTTAAA | 10451 |
rs367863890 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107705882 | AACTCTAACTCAGGT[A/C]TTTGCTTTTGGCCAC | 10451 |
rs367874868 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107827765 | TTAACCATTGATTTT[A/T]TTTGAAACAGTCTTA | 10451 |
rs367875582 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896242 | TTAAAAAGAAATCAA[C/T]TGATAAAGCTCTCCA | 10451 |
rs367878830 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786420 | CTAGCAAGGTAAGGA[C/T]GGGAGTCAAGATGAT | 10451 |
rs367892721 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107699226 | CCCAAGATACAATAG[A/G]GGTACAGGCATTGTG | 10451 |
rs367896157 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107768270 | TATGATACATCAGTT[-/T]ATTTCAAGAAAATAA | 10451 |
rs367901891 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107913089 | TATAGATTTTATCCT[A/G]TCAAGAGCACAAATA | 10451 |
rs367902943 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107921521 | CAGAACTACACATAC[A/G]GCCTGGACACAGTAA | 10451 |
rs367925764 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107766429 | TAAGACCCACAAAAC[C/T]TAAACTTCAAAAGTT | 10451 |
rs367969576 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107773572 | TAAAGACAGATGAGG[A/C]GAGGAACAGACAGAG | 10451 |
rs367974734 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728276 | CACTAACACAAGATC[C/T]GTTCTAAATGAAGAG | 10451 |
rs367974781 | snp | C/T | 1.68179e-05 | 0.00289977 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749474 | CACCTTTTTGTTTTC[C/T]TTATCGGTTGTAGGA | 10451 |
rs367976864 | snp | C/T | 1.67854e-05 | 0.00289697 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964794 | ACACCTGAGCCGAGT[C/T]CCAGGTCACCCGGTG | 10451 |
rs367977140 | snp | C/T | 0.0209421 | 0.100162 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591060 | AGTTCCTTAAAAATA[C/T]GAAGTTCTCTAATGC | 10451 |
rs367981015 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107737527 | AAAATCAAACAACCC[A/T]TCAAAAAGTAGGCAA | 10451 |
rs368018115 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822235 | CAATCTTGGAGCCCA[C/T]GGTTAGAAGAACTTG | 10451 |
rs368026212 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107826557 | AAAGGTATGAGGTCA[A/T]ACTTTCATTACTGCT | 10451 |
rs368027248 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107609727 | GGGCACTGGGCACTC[C/G]CATGCACACACACCC | 10451 |
rs368039542 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107818310 | TCCACATGGAGCTCT[A/G]CTGTGTTCCCTCAGA | 10451 |
rs368042060 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908886 | ACACAATATAAAACA[C/T]ATTCTGGAAGCATTC | 10451 |
rs368050736 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632098 | CAGTCCCACCAACAG[A/T]GTAAAAGTGTAACAC | 10451 |
rs368053188 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107666407 | TCTGCAATTTGGAAA[G/T]TGGTGTGTGGGCTTT | 10451 |
rs368059944 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107657721 | TAGCAAAATATTCTC[C/T]GGGATTCACAGAACA | 10451 |
rs368078011 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107841601 | ATACAAAAACACAAA[C/G]TAAAAGCATTAGATA | 10451 |
rs368078997 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814871 | TGAGAAACTCCAATT[A/T]CAACATCTTGAAAAC | 10451 |
rs368080047 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107778195 | TTCACATTGACTTAT[A/G]GATTAATTTAATACT | 10451 |
rs368084503 | snp | A/C | 0.000153988 | 0.00877328 | missense, intron-variant | VAV3 | GRCh38.p7 | 1:107683514 | TGTTTAGGAGTTCTT[A/C]GCAGTCCATTGGTCC | 10451 |
rs368087466 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107876823 | TACCAAAATAAAGTT[A/T]AAAAAAATGGAAAAA | 10451 |
rs368091734 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572836 | TTTAAGACAAGTAAG[G/T]CTGGATCTTTCCAGT | 10451 |
rs368095142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107924526 | CTGGTTACCTCTCAA[C/T]TTTTGTCAACTTCTC | 10451 |
rs368106207 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107577324 | TGTGCAACTGCCACT[C/T]TGCTTCAGGCACCTC | 10451 |
rs368107036 | snp | A/C | 3.47929e-05 | 0.00417076 | missense, upstream-variant-2KB, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107755498 | TTTTCACTTCATTCA[A/C]ATATTGTGCCAAGTC | 10451 |
rs368110231 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950022 | AGCTGGTTGCAAGAG[A/G]GGACAAACAGCCTGG | 10451 |
rs368119135 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107930717 | GATGAAAAGTCAATG[-/A]AAAACTTTATATTGA | 10451 |
rs368121115 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107917413 | ATAAGGGAACTAAGA[G/T]TCAACAAGTTAGGTA | 10451 |
rs368123107 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925919 | ATATGTTACATATAT[A/T]ACATACGTATATATA | 10451 |
rs368131234 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107584281 | ATTAAAGACTTAAAC[A/G]TTAGACCTAAAACCA | 10451 |
rs368149474 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107948021 | TTACCTGGCTTAAAA[C/T]AGCAAAACTGCTCTC | 10451 |
rs368187115 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866744 | AGGAGAATCACTTGA[-/A]CCTGGAAGGTGGAGG | 10451 |
rs368193930 | in-del | -/GTTT | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107683686 | GAATATGGTTTTAAA[-/GTTT]GTTTTATTTGTTTTT | 10451 |
rs368213561 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650386 | GAAAAAATAATCTGA[A/G]CTACTATTCTCACTC | 10451 |
rs368215888 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107827039 | AGTTAGTATGCTGTA[A/G]TAGTTTCTCATACTT | 10451 |
rs368217411 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107716322 | AACAGCCAGCCAGTA[A/G]AGACTTTTAAAAGTG | 10451 |
rs368217600 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107779504 | TAACCTGAGAAAAGA[C/G]GAAAATACTAATTAG | 10451 |
rs368217915 | snp | A/C | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107785989 | AGCTTAGTGTCACTT[A/C]CAGCAACACATCTTA | 10451 |
rs368227493 | in-del | -/CAAGTTCCAGGAAA | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963168 | GAGAGTTCCAGGAAA[-/CAAGTTCCAGGAAA]TGTGCACAGTACTGT | 10451 |
rs368228725 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107737623 | TCATCATCACTGGCC[A/G]TCAGAGAAATGCAAA | 10451 |
rs368240533 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107800966 | TCAAGTCTTAGATTT[A/G]AGTCTTTAATCCATT | 10451 |
rs368276859 | in-del | -/T/TT | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107742244 | CAAGTCTTTTTTTTT[-/T/TT]CCCACTTGTCTTGGT | 10451 |
rs368280339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107927641 | CATTGGTGGTAGTCC[C/T]GTAGTACTCCCTGTG | 10451 |
rs368282657 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840959 | GCAATCAAATAGCTT[A/C]TACGGGAAGGCTGGA | 10451 |
rs368283363 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107634986 | CAGGTGCTGGAGAGG[A/C]TGTGGAGAAATAGGA | 10451 |
rs368296347 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107820897 | GGCAAGTTTCTTTAA[C/T]ACCTATATAACCAAG | 10451 |
rs368297499 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107687336 | ACAAGCACCTCTTAT[A/G]TTTTGCTGTACTTTT | 10451 |
rs368298471 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107671676 | GGAAATAAGAACAAC[A/G]GGAGGAGCTACTCTG | 10451 |
rs368302932 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107800350 | TCCATATCCTCACCA[A/G]CATCCATTATTCCCT | 10451 |
rs368304749 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833634 | TTCCAAAAGTTCATA[A/C]TCTTTTTCAAGGGAT | 10451 |
rs368305758 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107761929 | TTTCACCCTCTTCTT[C/T]CCTAAAGGTTTATTT | 10451 |
rs368312280 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107815068 | TTTAAAATGAGAAAA[C/T]TCATGTTATTGAAAT | 10451 |
rs368326657 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107865069 | TGCAGTAGGGATCCT[C/T]ATCAGGGCCATTTTA | 10451 |
rs368329988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107573723 | CATCAGCAGTTCTTA[C/T]AGATATTTTGCAATA | 10451 |
rs368332084 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107687120 | ATGAAACACTAAAGG[A/G]ACTCTTTGGTTAATT | 10451 |
rs368342769 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107805246 | TCTTTGAATAATCTT[C/T]CTACTCCTCGCTCTT | 10451 |
rs368347734 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107573923 | CAGTTTCCAGAGGGC[-/A]GAGGCCTGTGGGCTG | 10451 |
rs368350497 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731698 | GCAATTTCAGAGGCA[C/G]TCCGTCCCTCATCAC | 10451 |
rs368356842 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107850988 | AAGTTATCCTGAATT[C/G]TAGGTGGCAATAAGC | 10451 |
rs368425828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107694360 | TCTAACAATTGGATC[A/G]ACTGGATCAGGCAGT | 10451 |
rs368444113 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107816443 | ATTGATTTCTTAATT[C/G]ATTAATACTGGCCAC | 10451 |
rs368462299 | snp | C/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786182 | TTGTTCAAGAGAGTA[C/G]AGTATCTATATAGGT | 10451 |
rs368467263 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736096 | ACATAAACAGAATCA[A/C]AGACAAAAATCACAT | 10451 |
rs368476916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107900021 | CAGCATACTTAATAT[A/G]TATCAGCAGGCATTT | 10451 |
rs368478280 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107754393 | AGAGACAGGTTCACA[A/G]TGTTTCAGAGAAAGC | 10451 |
rs368492930 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572279 | CCCTCTTTCTGTCCC[A/G]GAAATGAATAAAGGA | 10451 |
rs368494974 | snp | C/G/T | 8.51196e-05 | 0.00652333 | intron-variant | VAV3 | GRCh38.p7 | 1:107757243 | AATACAAACAAATTA[C/G/T]TGATGAATCTGCCCT | 10451 |
rs368497877 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814785 | AGTGCTTATGGAAGA[-/A]TATTCTAGCAGCAAT | 10451 |
rs368507836 | snp | A/G | 0.116488 | 0.211364 | intron-variant | VAV3 | GRCh38.p7 | 1:107922858 | TCGGGAGGCTGAGGC[A/G]GGAGAATGGCGTGAA | 10451 |
rs368546260 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107949203 | AGCTTGTTGCATTTA[C/T]ATGTAGTTTAAGAAA | 10451 |
rs368553077 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933224 | GTTTTGCTTACAATA[C/T]TCATATTTGCCAGAG | 10451 |
rs368558207 | snp | A/G | | | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107757268 | TGCCCTACCTTCATG[A/G]CATCAAGAGCCAGTT | 10451 |
rs368571419 | snp | G/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595513 | AATAAAGTGATATCA[G/T]ATTAAGAAAATAAAA | 10451 |
rs368575563 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107894038 | ACCAAACCAGTCAAA[G/T]CACACACAGAATACT | 10451 |
rs368620757 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107604355 | CCATCTAGTATAAAA[C/G]AGGAACTAAAGGCAT | 10451 |
rs368622708 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107619494 | CACTAGCCAGACCTT[C/T]ATATATAAACACACT | 10451 |
rs368625353 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107578668 | GTTTGGAGTGCAGTT[A/G]CACGATCTCGGCTCA | 10451 |
rs368627898 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107955887 | TCTGATCATCTGCCC[C/T]AGTAGCTCAGATCAA | 10451 |
rs368645301 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107672894 | ACAAGGTTGGTGGGC[A/G]TAAAATAAGACATAT | 10451 |
rs368653011 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107635484 | GTGGGGTGGGGGGAG[C/G]GGGGAGGGATAGCAT | 10451 |
rs368655622 | in-del | -/CA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107877130 | AAACCCTTTGAAACA[-/CA]AAGGCAGCAGGTAAT | 10451 |
rs368656345 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107698756 | ACTCCCAGTTTAACA[A/T]GGATGGGGAGGCCTC | 10451 |
rs368666307 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681397 | ATGAGGATCAAGGCA[C/T]GCTGGTCATCAAGCA | 10451 |
rs368685899 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713419 | TGTTTAGAATATGTA[C/T]GGTAAAAGATTAATC | 10451 |
rs368694308 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736602 | GTGAACTCCCATTCA[C/G]AATTGCTACAAAGAG | 10451 |
rs368702114 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726490 | AAGTCATTGATTAAA[C/T]TAATCAATCAATTAT | 10451 |
rs368704064 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107861967 | ATTCATTTTTCTAAC[C/T]TAATGATTTCTGACT | 10451 |
rs368712291 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107821610 | GGTAGACAGCTGACA[C/T]GTCCACAGTAAAATG | 10451 |
rs368729205 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107844996 | GGGTCCCTGACCCCT[A/G]TGCCTCCTGAGTGGG | 10451 |
rs368737145 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107684229 | CTACATATTTTATTT[C/T]TAAAGCATTAAACTC | 10451 |
rs368741199 | in-del | -/GT | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592057 | CATATATATACATAC[-/GT]GTGTGTGTGTGTGTG | 10451 |
rs368751436 | in-del | -/GTAT | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592081 | TGTGTGTGTGTGTAT[-/GTAT]CTTCCCAACCCCTGT | 10451 |
rs368768114 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933834 | AAAAAAAAAAAAAAA[A/T]TAAATCTCATTACTT | 10451 |
rs368769239 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107627954 | ACTGAGATAAAGTAA[C/T]GAAACCCATAGCTTT | 10451 |
rs368769571 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107958056 | ATGCCTAAAGATGCC[A/G]CAACTACTTTACATG | 10451 |
rs368777110 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892465 | GTTGTACAAATGCAC[A/G]TATCACTGCCATCTC | 10451 |
rs368778309 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590480 | ATAATTCTCACATCA[C/T]TATATTCTATGTGAA | 10451 |
rs368796349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711799 | TTCGAGCGATTCTCA[C/T]GCCTCAGCCTCCTGA | 10451 |
rs368804278 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107584070 | AGAGATATAGATCAA[A/T]GGAACAGAACAGAGC | 10451 |
rs368818772 | snp | C/G | 1.66905e-05 | 0.00288876 | intron-variant | VAV3 | GRCh38.p7 | 1:107603016 | ATGAAAACAGGAAAT[C/G]TATTTCTGTAAAAGT | 10451 |
rs368820332 | snp | C/T | 8.25021e-05 | 0.00642217 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107770678 | ATATTTTTCTTCTGT[C/T]TGCTTAATTTCTGCT | 10451 |
rs368853628 | snp | A/C | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786488 | ACAATTAAAACATCA[A/C]TTATCAAACAAGTTT | 10451 |
rs368855248 | snp | C/G | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107779542 | GTTCAGAAAATATAA[C/G]ATTTCTTTTTCCAAA | 10451 |
rs368856586 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107788828 | AATGTAATCATATTT[A/G]CAAATCCTTCTCTGC | 10451 |
rs368874471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690958 | AAGTCTGTTTTTATT[C/T]AATCATGTTTCATGG | 10451 |
rs368883486 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107886086 | AAAAGGCCTGGCCAA[A/C]ATTTTGGAGGAAATG | 10451 |
rs368883884 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107759834 | CACCAAAGTTACAAA[A/C]TAAATTATTACCTTA | 10451 |
rs368913635 | snp | A/G | | | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897404 | GAGAAAGAGAGAAAA[A/G]ACAAGAAGAGGTGAG | 10451 |
rs368914759 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945620 | TCTGAGGTCAAGCTC[A/G]AGACCAGCCTGGCCA | 10451 |
rs368914878 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107791604 | CACTAATGTCTAGAC[C/T]TTACCTTCAGAGAAT | 10451 |
rs368915634 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847867 | TTTGTACCATTCATT[C/G]TGAAGCTATTCCAAA | 10451 |
rs368919924 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107931490 | TAACCTAGATAACCG[C/T]TGAATCCAGGTGATG | 10451 |
rs368927708 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107813393 | ACAAAGGGATCCAAA[C/T]TGGCATACTGGCATA | 10451 |
rs368928143 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107817899 | TCTGAGTTTGCTCTC[C/T]GGACTCAACTTCACA | 10451 |
rs368938550 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107797676 | TAAAAAATCTCAGCT[C/G]TTAAGAAAAATCATG | 10451 |
rs368948966 | in-del | -/GAGA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952523 | AAAAGAAAGACAGGA[-/GAGA]AATACCTTGAGCCAT | 10451 |
rs368950602 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107766698 | CCACCAATAAAGAGA[A/G]AGGGAAAAGGAGAGT | 10451 |
rs368973784 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107627259 | CTCTGTGAGGTATCC[C/T]GGGTCTTCCTCAATC | 10451 |
rs368980859 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856267 | TAATTACGGTTTACA[A/T]CATTCCAGTGAAATA | 10451 |
rs369012482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579224 | GTTAGGCTTTGGCCC[C/T]GCTGCTGTCTTCACT | 10451 |
rs369018781 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107795346 | ATATCCTCGGTGCTA[C/T]ATAAAAACTCTTACA | 10451 |
rs369026545 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774591 | TTTTCAAATGGTCAA[C/T]AAATCAAAAACAATC | 10451 |
rs369026888 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922854 | CTACTCGGGAGGCTG[A/C]GGCGGGAGAATGGCG | 10451 |
rs369032401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107718050 | GTTTCATTGATGGAA[C/T]GTATCTCAAAATAAT | 10451 |
rs369033371 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107819387 | AAGAGAAAATGATAT[G/T]AGAGACAGGCACAGT | 10451 |
rs369040433 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107808972 | AATAATGCCAATCGA[C/T]GAAGGCATTTTTTAT | 10451 |
rs369041777 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753657 | CTCCGCCTCCTGGGT[G/T]CAAGCAATTCTCCTG | 10451 |
rs369060654 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107783762 | TGGCTTTTAAAAATA[C/T]TTCAGGCCAGGCCTG | 10451 |
rs369068435 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107605523 | CATGAGACAAATAAA[C/T]ATATCTTCTTTATAA | 10451 |
rs369075112 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107734235 | CGGAAAGGAACAACC[A/G]GTAACAGCCACTGCA | 10451 |
rs369125543 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107732257 | CGTTTCAAGATGACC[A/G]AATAGGAACAGCTCC | 10451 |
rs369139281 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107627662 | CTATGAGACTCACAA[C/T]ACTCCATGAGTCATT | 10451 |
rs369147329 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107660079 | AAAAAGTATTCCCAC[A/G]GATCATCTAATTCAC | 10451 |
rs369188757 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107953299 | TGGGGAGGCAGTGGG[A/G]AGAAGGAAGGAAATA | 10451 |
rs369190387 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650719 | CCCCCCCCTCCCCCC[A/C]CCCCACAACAGTCCC | 10451 |
rs369192444 | snp | A/G | 1.6599e-05 | 0.00288084 | intron-variant | VAV3 | GRCh38.p7 | 1:107777187 | ACCCACAATGGACAC[A/G]TAAATTGGCAGTGGC | 10451 |
rs369213847 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580286 | GCTCATCTTCTGCTC[A/C]CTTAAACTGCTCCAT | 10451 |
rs369221408 | in-del | -/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107632591 | CCCAAGTTACATCTG[-/T]ATGGGAAACACTAGA | 10451 |
rs369230961 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724130 | TTTTAATTAGGAAAA[G/T]GGTATCTCCAATCAT | 10451 |
rs369235639 | in-del | -/GAGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107915506 | ATCCTATGTGAAACT[-/GAGT]AAGTTACTTGATCTG | 10451 |
rs369239783 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107657225 | CTCCCAAAGTGCTGG[C/T]ATTACAGGCATGAGC | 10451 |
rs369241207 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107677922 | TCCTTTGTGAACTCG[A/G]AATGAGCCTTGAAGG | 10451 |
rs369251760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107696403 | ATAATTTATTCTTCC[C/T]ATCTGGGTGTACTTC | 10451 |
rs369256933 | in-del | -/ACCACA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928191 | TACAACTCTACAAGA[-/ACCACA]GCATTACTGGGTTTG | 10451 |
rs369261657 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107780907 | TCTACATGAGGCTTA[C/T]TCAGAATGATAGTAA | 10451 |
rs369262089 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107810984 | AATAACAGACTAGAA[A/G]ATACTCTCAAAACGG | 10451 |
rs369269358 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107652640 | ATATATATATTTATA[G/T]TGCCTAAATTTGTAT | 10451 |
rs369270144 | snp | A/G | 1.65195e-05 | 0.00287393 | stop-gained, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107751178 | CATCTCCCTGAGGTC[A/G]TCCAAAAAGCAAAAC | 10451 |
rs369276504 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107657201 | CTCAAGTGATCCGCC[C/T]GTCTCGGCCTCCCAA | 10451 |
rs369280617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880897 | TTTCGGTGCTTGCTA[C/T]GTGTCAAGCTCTATG | 10451 |
rs369283445 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107659622 | TTTTACATAACCTTC[C/T]TGGAATCTACAGAAA | 10451 |
rs369292410 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809039 | AAGGCTGAGCGCAAC[C/G]TGCCCAAAAGGAAGG | 10451 |
rs369296362 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107695670 | GAGAGAAGTTTCATG[C/T]ACAGATGGACCTTTA | 10451 |
rs369300329 | snp | C/T | 9.12101e-05 | 0.00675253 | intron-variant | VAV3 | GRCh38.p7 | 1:107704934 | TCAGTTCCTTTAAAC[C/T]GAAAACCAGGACTGA | 10451 |
rs369301633 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107828954 | CTGAACTACATCATT[G/T]GCAAAGCCCCTTTCA | 10451 |
rs369315638 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857361 | CTCAGCTTGCAGACA[C/G]CCTATTGTGGGACCT | 10451 |
rs369327080 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107869623 | CAAACCAAGATCTAA[C/T]TCAGAAACCATGTAT | 10451 |
rs369327906 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107851716 | GGAAATAAACATATA[A/G]TAGAGAAGATTTTTT | 10451 |
rs369330242 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107872927 | GTTTTTACTTAGAGT[A/C]TATAATGCTTAATAC | 10451 |
rs369339948 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871489 | TTACTAAACTCACTC[C/G]TCTTTCCTGTGTGAT | 10451 |
rs369342681 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107806054 | ACTTGGCATCTCCTT[C/T]GGCCAAGTTACAAAG | 10451 |
rs369342833 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871558 | ATTTTTGTTGATGTT[A/G]GTGGAGTTTGAAGTG | 10451 |
rs369361092 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107943691 | AGGTTGCAGTGAGCC[A/G]AGATGGTGCCACTGT | 10451 |
rs369376412 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107938882 | AACCTACTCTTGTAC[C/T]AATCACAGAGTTTCA | 10451 |
rs369378478 | snp | A/G | | | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897640 | AGGTGCATTCACCCT[A/G]CCCATGACACCACGG | 10451 |
rs369380491 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940472 | CAGGACATTTGAAAG[-/A]TAGAGAAGGTTCTAC | 10451 |
rs369388946 | in-del | -/CAAAAAACAAAACAAAAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764112 | AAACAAAACAAAAAA[-/CAAAAAACAAAACAAAAA]AAAAACATGATGTAC | 10451 |
rs369389772 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570789 | CCTGTCCATTCAGAA[C/T]GGCGCTCACCTATTT | 10451 |
rs369393801 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107620440 | CAGTGCAGTAACATG[C/T]GATACAGGTTTGTAG | 10451 |
rs369403747 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702031 | TATAGCAGTGCCCCC[A/C/T]ACTCTGGGTACCAAT | 10451 |
rs369403950 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650965 | TGCAGCCATAAAAAT[A/G]ATGAGTTCATGTCCT | 10451 |
rs369422777 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580825 | TTAGAATGATTTAAC[C/G]TGTAAAATATATTTC | 10451 |
rs369427385 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107880820 | AAAGAAAARAAAAAA[-/A]AGCACCAAAGGAAAG | 10451 |
rs369437644 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107743153 | AAAACCAGTCAGGGC[C/T]TTCTTCCATCCTAGC | 10451 |
rs369445477 | snp | C/T | 8.32979e-05 | 0.00645306 | intron-variant | VAV3 | GRCh38.p7 | 1:107704509 | TTAGCAAATTTTATG[C/T]CCTCATTAAAAACAG | 10451 |
rs369450512 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107633894 | GTGGACACGGGCATT[C/T]GAGACCTTACAGCTG | 10451 |
rs369490609 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107603713 | CTTTTAAAAGGTAGA[A/T]TTTTTTTTTTGCATA | 10451 |
rs369495434 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107717169 | GTCTATCTATTTTGT[C/T]GATCTTTTCAGAAAA | 10451 |
rs369511103 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107878063 | TTGAATTTCAGAACA[A/C]AAGTTGAAAGAATAC | 10451 |
rs369514094 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107659047 | TGTCCTGAATGGTAA[C/T]GCCTAGGTTTTCTTC | 10451 |
rs369535146 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713186 | ATGAGGCTTATATTC[G/T]GCATTTAAATGTAAA | 10451 |
rs369558850 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107598216 | AAAAAGTTAGCCAGG[C/T]GTGGTGGCAGGTGCC | 10451 |
rs369564839 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928200 | ACAAGAACCACAGCA[C/T]TACTGGGTTTGGGGT | 10451 |
rs369572724 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107815624 | TGATAGAGATGCTAA[C/T]GAGAATGGCTTATAA | 10451 |
rs369597348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107697815 | GAACATTCAAACCTA[A/T]AAACACTGGGTAGTT | 10451 |
rs369605839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107926655 | AGAGTGCAGCAAGCG[C/T]GAGGCATTGCATTTA | 10451 |
rs369605929 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107584643 | TCATTTAATTGAATG[C/T]TGACATCTGGTAAGT | 10451 |
rs369609072 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107764086 | TCAGGAAAAAAAAAA[-/A]CAAAAAACAAAAAAC | 10451 |
rs369625482 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107950258 | ACTCTCTCTGGGAAT[C/G]AGAAGGCAAAAATGT | 10451 |
rs369626614 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107611492 | ACAAGATATACATGG[C/T]TTCTGAAATGTGATG | 10451 |
rs369653302 | snp | A/C | 0.000263135 | 0.0114673 | utr-variant-5-prime, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964871 | TTCCACGGCTCCATG[A/C]CCGACGGCTCCGGGA | 10451 |
rs369661454 | snp | A/T | | | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690183 | CCATAGAAGTGTTTT[A/T]AGGTCCTTGCAAAGT | 10451 |
rs369667622 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107800949 | CGAGTAGTTTCACAA[C/T]TTCAAGTCTTAGATT | 10451 |
rs369667906 | snp | A/G | | | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587686 | ACCTCCACTTCCTGG[A/G]TTCAAGCAATTCTTC | 10451 |
rs369670224 | in-del | -/AATGGCATGTCAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892137 | TGATTAATATGTCAT[-/AATGGCATGTCAT]TGTTAGCAGAATTGT | 10451 |
rs369670462 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702810 | CAAAAAAAAAAAAAA[A/T]ACCTGATTTTTCACT | 10451 |
rs369679957 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107727492 | ACCTCCAAACACCTT[C/T]ATGAAATCAGGTTTA | 10451 |
rs369682730 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713893 | AAAGTCAGACATCAC[A/G]TTTTGGCTAGTCAAA | 10451 |
rs369690470 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107676684 | GTATATAATTGAACT[C/G]ACCCAAACCTAGGAA | 10451 |
rs369709212 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107829327 | CTGTTCCCCTGATTT[A/T]TATAGCTTTTATGTG | 10451 |
rs369715948 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107805780 | GTTTTGTTTTTTGTT[A/G]GGTATGTTTGCTTAT | 10451 |
rs369720084 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107648295 | GCACTGTCTACTGGA[A/G]TATTAGTGAATCATG | 10451 |
rs369723902 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107616386 | GTGAAAGTTAAAATT[G/T]AGTATACATGGACAT | 10451 |
rs369731484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107814174 | ATAAATACCCAGTCA[A/G]TAGCGAAAACTGCTG | 10451 |
rs369795002 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107633958 | GAACCACCTTATCAC[C/T]CATAGCATTATGAGA | 10451 |
rs369795638 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107919442 | TTAATATAAACTGGA[A/G]AGTTGTCTAAAACCC | 10451 |
rs369799294 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954535 | GTATCCTGAGGCAAA[-/T]TTTTTTTTTTTTTTT | 10451 |
rs369801725 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107910248 | AAGCTTTTCCATACA[C/T]GGATAAGAACATAAA | 10451 |
rs369803006 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929555 | ATAACATTGTAACTA[C/T]AGTAAGTAAACTCCC | 10451 |
rs369803231 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107884108 | GCCAGAAGACAGCTA[A/G]CTCAAAGCAACCCAG | 10451 |
rs369826971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902431 | TTGTAAGCAATTATA[C/T]AATGTTTCACATTCT | 10451 |
rs369838331 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107739407 | AGTATAGTTCCCTAT[A/C]CTGACTTAACTGCCA | 10451 |
rs369841713 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107758695 | TATAAATCAGATCCT[C/G]TCTCTACCCTACTCA | 10451 |
rs369854905 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107647519 | ACAGGTGAACTCTGA[C/G]ATAACAATACAACTG | 10451 |
rs369861171 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107683551 | GTGCAGTAAAGTAAA[A/G]CAAAGCAAAACAAAT | 10451 |
rs369862001 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950825 | GTCAACTAAAGAGCA[A/C]AGGGAGGATAATGGC | 10451 |
rs369867371 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107761160 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCACAAGG | 10451 |
rs369867456 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107698481 | AGCTATAATGTACAA[C/T]AGGTTAGGTGCATTG | 10451 |
rs369868395 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107741027 | TGAAGAAAATGAAAA[A/T]GAGGAGAGAGGAGGG | 10451 |
rs369877709 | in-del | -/TCTC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107742173 | ATACAGGAAAAACTC[-/TCTC]CTCCAAAGGGCTGTT | 10451 |
rs369891971 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107690794 | AGGGCTTCCCCTTTG[C/T]CTTTCTCCTTGCTAT | 10451 |
rs369898057 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107703757 | TTTGAACTCAAGCTG[C/T]TAAAGATCCTTTCTT | 10451 |
rs369911802 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892946 | TTAACATTAGGCTGA[-/G]CACTACCTGGCCTCC | 10451 |
rs369913176 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107742748 | TTATTCTTTAGGAGA[A/G]AAGAGAAGTAAAACT | 10451 |
rs369919561 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107631046 | AGAAGACTATATCAA[A/G]TTCGGTACAAAGACT | 10451 |
rs369932671 | snp | C/T | 2.59879e-05 | 0.00360462 | intron-variant | VAV3 | GRCh38.p7 | 1:107749108 | TTCCTTAGATTAATA[C/T]GTATCATTAATAACA | 10451 |
rs369936407 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107829077 | TCTGCTTTCCTTTCC[A/C]GCCATGTAAATTGGT | 10451 |
rs369960624 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107758056 | ATTCCCCAAACTTAA[-/T]CAATCTTCACCCAGA | 10451 |
rs369978694 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107905834 | AAAGTATTCTATTCT[A/G]GTTAGAAAATGTTAA | 10451 |
rs369994121 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107740022 | CTGGGCATGGTGGCT[A/C]ACGCCTGAAATCCCA | 10451 |
rs370002366 | snp | C/G/T | 5.09276e-05 | 0.00504595 | intron-variant | VAV3 | GRCh38.p7 | 1:107751102 | ATTTTGAAAATAGTA[C/G/T]TCTTCTTTTCTTACC | 10451 |
rs370005200 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107850726 | AAGTATAATTTTTTT[-/A]AAAAAAAAGAAAGAA | 10451 |
rs370009450 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107894144 | TATAGTTGACTGTAA[A/G]TGGACACTGTTTACT | 10451 |
rs370009919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868288 | CACCCTAAAATAATT[A/C]TTCCTGTTTACATAT | 10451 |
rs370015861 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921989 | CTTCAACCTGCCTCA[C/G]AAACATGACCCAAGG | 10451 |
rs370016412 | in-del | -/ACAGAAGGA | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107880408 | TGGACAAGAGCGCTG[-/ACAGAAGGA]ACAGAAGAGGGGAGC | 10451 |
rs370027221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586311 | TGCCTGCCCTGAAGT[A/G]GGCTCTCAATTAAGA | 10451 |
rs370028055 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107857999 | TATATAGTAACAACA[C/T]AGGTAAAGAAAATGT | 10451 |
rs370030619 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107931177 | AAGAAATCTGAATAC[A/G]GACTGTATGTTAGAT | 10451 |
rs370031265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625235 | CTTAATTAGGGATGA[C/T]GTGTGTCAGTAATTT | 10451 |
rs370034281 | snp | A/C | 0.0170251 | 0.090679 | intron-variant | VAV3 | GRCh38.p7 | 1:107879429 | TTTCTTTGTGGAGTG[A/C]ATAATAAGCCAATTC | 10451 |
rs370034553 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107597226 | TTTAAAAATAAAAAA[-/T]AAAAAAAAAAAAACA | 10451 |
rs370044921 | snp | C/G/T | 4.00924e-05 | 0.00447715 | intron-variant, utr-variant-5-prime | VAV3 | GRCh38.p7 | 1:107785511 | TGCTAGAGCCCCAAA[C/G/T]GCAAGACGAGCTTGG | 10451 |
rs370045695 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107680544 | CACCTTTGAGAGTAC[C/T]TTACTTGCTCTTTTG | 10451 |
rs370054321 | in-del | -/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107601789 | TATTTTTTTTAAACT[-/TG]GGGAATAATCCTTAT | 10451 |
rs370054516 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702795 | TAAGCCCACGTCTTT[A/C]AAAAAAAAAAAAAAA | 10451 |
rs370057233 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107771737 | AAATTATTATCACTG[C/T]TCACCCCATCAGCTG | 10451 |
rs370060569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632075 | TCCACAATGGTTGAA[C/G]TAGTTTACAGTCCCA | 10451 |
rs370061329 | snp | A/G | 8.34801e-05 | 0.00646012 | intron-variant | VAV3 | GRCh38.p7 | 1:107874891 | AGTGTTAAAAATGAA[A/G]TATAATTACCTTTCC | 10451 |
rs370085582 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107666317 | TCTTAAGGGAAAAAA[-/A]TATAAGAGTTAATGT | 10451 |
rs370096510 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963820 | TTCTGTACAAAAATT[C/T]TCCGACAGGACAAAT | 10451 |
rs370129121 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107727910 | TTGAATATGGAATTG[A/C]AAGCTGGACTGTGCG | 10451 |
rs370138397 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107616522 | CACAATAATCTGTAC[A/C]CCAAACCCCCATGAC | 10451 |
rs370145912 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107768062 | TAGGGGAAACTGATA[C/T]GGTGAGGACATCACC | 10451 |
rs370165567 | snp | C/T | 1.65386e-05 | 0.00287559 | intron-variant | VAV3 | GRCh38.p7 | 1:107609881 | TAAGGCATCCTGGAG[C/T]TAAGGGTATGGTATT | 10451 |
rs370166897 | snp | G/T | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107603096 | TCCTGTGCCTCACAA[G/T]GTAAGTACTATTTAC | 10451 |
rs370181791 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933022 | CAGCAATAGGAAACT[A/T]ATACATATCCCAATG | 10451 |
rs370190905 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107741498 | CAAAGACCAGTGAAA[-/C]CAGCCGAGGGAACAC | 10451 |
rs370192942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625353 | CTCACTGCAACCTCC[A/G]CCTCCCGGGCTCAAG | 10451 |
rs370193640 | snp | C/G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847173 | GCTCCTGAACGACTA[C/G/T]TGGGTAAATAACGAA | 10451 |
rs370205249 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107587300 | CTGCAGAGTTAAAAC[C/T]TGCTACCTTATGCAG | 10451 |
rs370222450 | in-del | -/A | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588130 | GGCTCAGAATAAAAA[-/A]TGCTTTAGAGTAGCT | 10451 |
rs370224254 | snp | C/T | 8.76501e-05 | 0.00661947 | intron-variant | VAV3 | GRCh38.p7 | 1:107602518 | TTATGAATATAAATG[C/T]GTTTTTAATCAGTAG | 10451 |
rs370236484 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107858687 | TTCACCCCCAAACCA[C/T]TCCCCCAGTACTCGG | 10451 |
rs370269434 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923594 | ACTTACAATCATGGA[C/G]GAAGGTGAAGGGAAA | 10451 |
rs370275361 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954395 | CTCACTTTCTCTCTT[C/T]CCCTCATTAACTTTC | 10451 |
rs370276914 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107766423 | ACAAGCTAAGACCCA[A/C]AAAACTTAAACTTCA | 10451 |
rs370278406 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840922 | TTCAGAGATGCTTTT[A/T]AAAAAAAAAAAAATT | 10451 |
rs370296161 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107628600 | ACTCTTCCTGTTACA[A/C]AAAAAGTTATACATA | 10451 |
rs370297074 | snp | A/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591458 | GAATGAATGAATGAA[A/G]CAAATCCAATGAGGT | 10451 |
rs370300936 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893062 | AAAATATACACAGAG[A/T]AAAAAACTTGGTCAA | 10451 |
rs370301756 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107576705 | ATCTTTGAACCCCAT[C/T]CATCCAAGGATGGCC | 10451 |
rs370301920 | snp | A/G | 4.32339e-05 | 0.0046492 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755562 | CACACTAAGATTAGA[A/G]ATGCAAACTGCTTTG | 10451 |
rs370303613 | snp | C/T | 0.000210224 | 0.0102503 | intron-variant, utr-variant-5-prime | VAV3 | GRCh38.p7 | 1:107785546 | TCAAGAAGGGGTCCA[C/T]GGCATCACACCCCTA | 10451 |
rs370311866 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769128 | TTCATAGCACTAATT[C/T]CAAGGAATTGGGTCA | 10451 |
rs370313126 | snp | C/T | 6.6189e-05 | 0.0057524 | intron-variant | VAV3 | GRCh38.p7 | 1:107768428 | CAATTTTAGCTAGCA[C/T]ATTTTTACTCACAGG | 10451 |
rs370319539 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107931788 | CAACTAGCATTACAC[C/T]ATGGAAGCAGCCCTA | 10451 |
rs370323788 | in-del | -/AA | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107709415 | AAGTAAAGGAAAGAT[-/AA]GAGACATTTTTATTA | 10451 |
rs370337952 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832424 | TGGAATTCGTGGACC[A/C/G]GGTCTTTAACAGTCT | 10451 |
rs370338644 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107652075 | GCTGCACTCCCAGAC[A/G]GTTAAGGCATTCTAA | 10451 |
rs370344091 | in-del | -/ACAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107718417 | ATACACCAATTACAG[-/ACAA]ACAGAGAGCCAAATC | 10451 |
rs370349801 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107737555 | CAAAGGATATGAACA[A/G]ACACTTCTCAAAAGA | 10451 |
rs370371925 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856895 | TTTTAAAATTAGCTG[A/G]GTGTGGTGTTGTGTG | 10451 |
rs370403532 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107716568 | TTGAACCAGCCTTGC[A/G]TCCCAGGGATGAAGC | 10451 |
rs370403837 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107725421 | AGCCGAAAGTAAAGA[A/G/T]AGTGAGAGGGACACT | 10451 |
rs370423687 | in-del | -/AG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107841091 | AAAGGGAGACCACTC[-/AG]GGGAATGATGATGGG | 10451 |
rs370430696 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107888392 | CTTTCCCCAACTACA[A/G]AGGAGAACACCACTT | 10451 |
rs370445201 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107785240 | TATGGCTACCTTTAA[A/G]GTCCTGAGTTAAGAA | 10451 |
rs370463053 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107782082 | CACTGTTAGAAAGCT[A/G]TGGGGTGAAATCTGC | 10451 |
rs370463075 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710154 | CAAATCCTAGCAAGA[C/T]GAAATCATCTGTAAT | 10451 |
rs370473967 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107735827 | CCAATCAATAGAAAA[A/C]GAGGGAATCCTCCCT | 10451 |
rs370487020 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107745202 | GTGACAAAAAAAAAA[-/A]TAAAACCCTTTTGGA | 10451 |
rs370493675 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107613387 | TCCATTTTCTGTTTT[A/G]TTTTTAACTTCTTAA | 10451 |
rs370509362 | in-del | -/GTTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107949324 | TTTGTTTGTTTGTTT[-/GTTT]TGAGACAGGGTCTTG | 10451 |
rs370529666 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107652791 | TTTATTTATTTGTGC[C/T]TCTACCCAACTATCA | 10451 |
rs370529901 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724815 | AATTCAGTCTGGTTG[C/T]AACACTGGATGTGGT | 10451 |
rs370548913 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107601724 | TATACACATTGTTTA[A/C]ATGACATACACAAAA | 10451 |
rs370563006 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107634069 | ATTTATAGATTCAAT[G/T]CCATCCCCATCAAGC | 10451 |
rs370579313 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107739549 | GCAACTGATGGTGCC[-/C]GGCATGGATTCTGCA | 10451 |
rs370588259 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107926584 | TGCCACCCCTCCCCC[A/C]TCTCCTGGTAGTAGC | 10451 |
rs370589218 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621844 | ATCTGATATACCATA[C/T]GGTGCTATCTTTATA | 10451 |
rs370601141 | snp | A/G | 1.72323e-05 | 0.00293528 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107766501 | TCATTTTTATTTACA[A/G]TGGAATCATGAATCT | 10451 |
rs370608378 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107782653 | CTATTGTACACTGAG[C/T]CCATCCGTTAACTCT | 10451 |
rs370628545 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107603195 | CACAGAAAATTTGGA[C/T]AATATACCTGGAAGA | 10451 |
rs370639156 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107859993 | TCCTTATTTTGACGG[C/T]TGTACCATTTGAAGT | 10451 |
rs370644519 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945495 | GAATAAAAATATAAG[C/T]GGCCCCTGCCATCGT | 10451 |
rs370660923 | snp | C/G | 1.65946e-05 | 0.00288046 | intron-variant | VAV3 | GRCh38.p7 | 1:107875059 | ATAAAGTTAATTATT[C/G]TGAATGCTATCCACC | 10451 |
rs370668561 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571993 | TTTTTTTCCCAACAT[A/G]TAACTCTCTCAGTCT | 10451 |
rs370672673 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575019 | CGCGCGCGCGCGCAC[A/G]CGCGCGCGTGTTTAA | 10451 |
rs370673733 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107805797 | GTATGTTTGCTTATA[A/G]ATTCTTTGTAATTTA | 10451 |
rs370694919 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107775298 | GTTAAAAAAGAATAT[C/T]GACTGGGCACAGTGG | 10451 |
rs370705881 | in-del | -/AAGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107793033 | AAAATGACGATAAAT[-/AAGT]GTCATTATATGTTAT | 10451 |
rs370736298 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809490 | GCTCTAACTTATAGC[C/G]AAGTCAAATTGCAAA | 10451 |
rs370743556 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107860955 | CTACAGAAGGTGTAG[A/C]AATTAATTCTGTGCT | 10451 |
rs370757254 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107885226 | ACATTCAAAATGAGG[G/T]AAAAGGTGACACATA | 10451 |
rs370762482 | snp | G/T | 1.65468e-05 | 0.00287631 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574054 | CAACTTACCCTGCCA[G/T]TTACTTCTCCTCTCC | 10451 |
rs370770329 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107865397 | TTAAGCAGTGTGTGT[A/G]TGAGTGTAATGAGTG | 10451 |
rs370778342 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107927993 | GCTATACTGGCTTCA[C/G]AGCACAGTCCCGGTG | 10451 |
rs370798506 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107739996 | ATCACTGATTAAACA[A/G]TGCTTCTTGGCTGGG | 10451 |
rs370801613 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819701 | CATAATGCCTTTAAA[A/C]ATATATACACCGCCA | 10451 |
rs370805461 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951708 | CATGCAGTCAACAAG[A/C]ATATGAAAAAAAGCT | 10451 |
rs370810281 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107686651 | CAAAACAGAGATTTT[C/T]AGTACAGTCACACAG | 10451 |
rs370815345 | snp | A/G | 6.61605e-05 | 0.00575116 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107875012 | TATGTTCTTCAAACA[A/G]AGAAACTGAGGAATG | 10451 |
rs370821657 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107729564 | GGTGCACTGAAGGGG[-/G]CATGGGTACGGAATC | 10451 |
rs370853413 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107807886 | AGCAGGAACAGAAAC[A/T]GATCAAATGGTACTG | 10451 |
rs370855903 | in-del | -/GAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107672292 | AAAAAAAAAAAAAAA[-/GAT]AAATTTAAATTCTGT | 10451 |
rs370857108 | in-del | -/AAAC | 0.0482946 | 0.147699 | intron-variant | VAV3 | GRCh38.p7 | 1:107849877 | CACATTTACAAGAAA[-/AAAC]AAACAAACAACCCCA | 10451 |
rs370872736 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796421 | TTCTCTTAGAAAAAA[C/T]AAGACATGTATACTG | 10451 |
rs370898320 | in-del | -/AAG | 5.83788e-05 | 0.00540241 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755540 | AAAGGGTAGAAAAAG[-/AAG]GCACACTAAGATTAG | 10451 |
rs370903880 | snp | A/G | 1.87106e-05 | 0.00305859 | intron-variant | VAV3 | GRCh38.p7 | 1:107704913 | CTGAAACACTTAGCA[A/G]TTATATCAGTTCCTT | 10451 |
rs370906522 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107682913 | ATAATGGATGAAAAA[C/T]AATTATACTAACATA | 10451 |
rs370912330 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732657 | CGGCAGACTGGCTGG[A/G]GAAGGGGCATCTGCC | 10451 |
rs370912657 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107715845 | CAAACACTGCAGATA[A/G]CATGAATTAGGAATG | 10451 |
rs370918199 | in-del | -/GTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107750014 | GCCTTGAGAAGTGTT[-/GTT]CATCCCTTTCACAAA | 10451 |
rs370944251 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107835988 | GGAAACACAGGCATG[G/T]TGCCTAAATATATAT | 10451 |
rs370952769 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724574 | GTGATTCCCAAAGGT[A/G]TAAGATATGGTGGAG | 10451 |
rs370957503 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107719238 | AAAGAGCTTCTGCAC[A/G]GCAAAAGAAACTGCC | 10451 |
rs370960685 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107748000 | TCTTTATAAGCGTAA[A/G]TAGTTTGGCTATAGA | 10451 |
rs370969689 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962728 | CCCTCTCATAGGACA[C/T]TACAGGAGAAACTGT | 10451 |
rs370987174 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107735305 | TAAAAGAACTAGAGA[A/G]GCAAGAGCAAACACA | 10451 |
rs370995480 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107695102 | TAGATACACAGACAT[A/G]AAAAAACTGGTTGGA | 10451 |
rs371002866 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107677020 | GCCTCAAAGGAAAAA[C/T]GATCCATAAAAACAA | 10451 |
rs371003990 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107678625 | AAGAAATCAACAATT[A/C]TGTTTAGACTTGGAA | 10451 |
rs371005839 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723576 | TCCAGCTTCTGAGTT[G/T]AAGCTATATTAGATC | 10451 |
rs371017599 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107646209 | GCAGTGATTAATTGG[-/A]AAACAGACAGTCATA | 10451 |
rs371048735 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920853 | TATATATATCTCCTT[C/T]GTAGCTTTTAAGCTA | 10451 |
rs371056622 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107704823 | AGGCAGAAAGCCTGG[C/T]AAAGGTTTGTGGGAT | 10451 |
rs371058848 | in-del | -/CA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107819549 | ATGACACAAATATGA[-/CA]AAGTGTTAATATCTC | 10451 |
rs371067950 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722206 | TATTAGATTGATCCT[C/T]TATTCCTGCCTTTCT | 10451 |
rs371068556 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107648627 | CATCTTCTTTAAAGA[C/T]AGAAAAAGAACACAA | 10451 |
rs371069206 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107682018 | AAGTTTATTCTTCAT[A/G]AAGTTCTAAAGTCTT | 10451 |
rs371088930 | snp | A/C | 0.000210694 | 0.0102617 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749072 | GAGGTAGAAGCCATA[A/C]GACCACTGTTAAAAT | 10451 |
rs371119678 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764214 | CTACGTGCCACCTCT[A/C]AAACTTTCCCAACTG | 10451 |
rs371121641 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107853513 | TTCATAAATGAAAAT[G/T]TATCACCTTCTGTAC | 10451 |
rs371130090 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941301 | GGTCTCTGCGTAGTA[C/G]AGTCATCATCTTCAC | 10451 |
rs371132485 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107899675 | TGTTACTTCATCTAA[C/T]CTTCAGGATTATTTT | 10451 |
rs371135604 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107709165 | CAGTAACTTTGTACC[A/G]CCCTAAAAGTAGCAC | 10451 |
rs371139589 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107932743 | CAGAACAGGAGAAAG[C/T]AATGTTGTGATGGAA | 10451 |
rs371146221 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107830533 | CTCTCACTTCACAGG[C/T]AGCCCCAGCAGCATG | 10451 |
rs371151671 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895725 | ACAATAAATAATAGA[A/G]TAGCATTTTTATTAA | 10451 |
rs371156655 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107841224 | AGGATATGGTAACAT[A/G]GCAGTGAATACAGCA | 10451 |
rs371161900 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107874290 | TGTTTAGTGTGCATA[C/G/T]GGATAACAGTAAATA | 10451 |
rs371163574 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107868018 | GTATGGGGTTGAGAA[-/A]GGGCTGAAAATACAA | 10451 |
rs371166552 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107727757 | ATATCAAGAGTCAAT[A/T]CAAACCTAATACTAA | 10451 |
rs371172857 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107931630 | ATGGATATTAAAACA[C/T]GTGATTGAAATATTG | 10451 |
rs371173296 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107853815 | GTAAACCAAGAAACA[C/G]TATTTTAACTCCTTT | 10451 |
rs371182271 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107730570 | CTTGAAATAAATTAA[C/T]TTGTAAATTAAGATT | 10451 |
rs371189363 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107832196 | CATGGCCAGGGAAAC[C/G]TTGCTAATGATCTAA | 10451 |
rs371203483 | snp | C/G | 1.68437e-05 | 0.00290199 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107779452 | ATTCCTGTGGCCAAT[C/G]CTATAGGTGTTCGAG | 10451 |
rs371215948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699221 | TTCCTCCCAAGATAC[A/G]ATAGGGGTACAGGCA | 10451 |
rs371241020 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891187 | GGACAATAAATTGCA[C/G/T]AGTCATTCATCTTTT | 10451 |
rs371244229 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907354 | GAGCCATTCAAAAAG[A/C]TGTTGACAATATCGT | 10451 |
rs371252725 | snp | C/T | 0.000118302 | 0.00769007 | intron-variant | VAV3 | GRCh38.p7 | 1:107874859 | CAATTTGCTTAAATG[C/T]TTTCCAGTTAAAAAG | 10451 |
rs371260684 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107705338 | TAACAAATGGCCACA[A/T]AGGTCAACCTGCCTG | 10451 |
rs371266110 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107913301 | CACAGACATAAAATG[C/T]CCATTTGGAAGATGT | 10451 |
rs371269175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786734 | ATAGTACACAGGATG[A/G]GCTCAGAGAAGCCAC | 10451 |
rs371277687 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107877931 | CTCTGTGCACATATA[A/G]GAACAGAGCTGAGGA | 10451 |
rs371284909 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658158 | CAATAATACAATATA[C/T]AGCTAAAGAATAACA | 10451 |
rs371287831 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107766276 | TTTTTCTTTTTTAAT[C/T]ACATATATAGAACTC | 10451 |
rs371302195 | snp | C/T | 3.29919e-05 | 0.00406138 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107777259 | GAAGGCCTTTGTAGA[C/T]GTCTTCATCATTAAT | 10451 |
rs371330854 | snp | C/T | 6.60644e-05 | 0.00574698 | synonymous-codon, intron-variant | VAV3 | GRCh38.p7 | 1:107683528 | TCGCAGTCCATTGGT[C/T]CGTTTCTGTGCAGTA | 10451 |
rs371343756 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107758466 | AGTCTCAGCTACTTG[A/G]GAGGCTAAGGCAGGA | 10451 |
rs371350571 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107865801 | CTGCCTCTCTAAAAG[G/T]GATAACTTGGCAGCT | 10451 |
rs371356198 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107876343 | TTTCAGAGACAAAGA[A/G]AGAAAAGGAAGTGAA | 10451 |
rs371370027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894275 | AGATCTCACTGCAGA[A/G]AGCAAATTTTAAAGC | 10451 |
rs371370603 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107666124 | TTAGCCCTTCACCTT[A/C]CCCTTCCTCTTCACT | 10451 |
rs371376934 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693799 | AACAGCAAAGGAGCA[C/T]ATAATCTAACAGGGG | 10451 |
rs371381191 | multinucleotide-polymorphism | AT/CC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107826216 | TACTATATTGTAAAT[AT/CC]CTATCTACACGATTA | 10451 |
rs371399197 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107865750 | GGGTTCTCCCAGCCA[C/G]TAGGACTGTCAGGTG | 10451 |
rs371399874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797283 | CTAGTTTGCCTCTTA[A/G]TAATTCTTAATCTTG | 10451 |
rs371403429 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774922 | CATTTGCTTTTTTTT[G/T]TTTTTTAAGATAACC | 10451 |
rs371404340 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107826087 | GTCTCCACTTGTACA[A/G]GTTTATCTTGTTATT | 10451 |
rs371409129 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107862473 | TTTCTAGGAGATCTT[A/G]TTGATAGGAAATACA | 10451 |
rs371423961 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107802627 | GTTCTTGGTTAGGTA[A/C]AGAGGATACATTACA | 10451 |
rs371433663 | snp | A/C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957378 | CGCCTAGTTTTGTCC[A/C/G]ATCCAATCCACCCCT | 10451 |
rs371451061 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588868 | TTCTCTTATTCCATA[C/T]AAAATATTTAATACA | 10451 |
rs371455532 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107925874 | ATATAAACAGATATG[G/T]CACATATAAATATAT | 10451 |
rs371463767 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107904749 | AATGCATAGAAGAAA[A/C]ATTTCTCTACCATCA | 10451 |
rs371463920 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107916530 | AATAAGACATTAAAG[A/G]AAATATTAAAAGCTT | 10451 |
rs371478826 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107914483 | ATCACTCCCCAGTGA[A/G]GATTAAACAATTTCT | 10451 |
rs371481327 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107606958 | GGGTAGGAGTCTGAT[C/T]TTTTTTTTTTTTTTA | 10451 |
rs371503503 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107956016 | AACGGCATACATGCA[C/T]GCAAATGGGAAAGAT | 10451 |
rs371525481 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107706799 | TGAGTCCTGGCAACC[C/T]GAAAAATTCATCAAC | 10451 |
rs371529988 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107711578 | AAAGATAGCAAATTC[A/G]AGCTTGCTATGTTAA | 10451 |
rs371541597 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107839253 | GCTTATGACCAAATA[C/T]AAAACTGATAACCTA | 10451 |
rs371548347 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107717076 | ATTTCTGTGGGATCG[A/G]TGGTGATATCCCCTT | 10451 |
rs371549480 | in-del | -/CAAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726499 | ATTAAATTAATCAAT[-/CAAT]TATCTACATAATAAC | 10451 |
rs371570927 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107714353 | AGTCATAGGCACTCC[A/T]AAAATCTCCAGTTCT | 10451 |
rs371573337 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107597992 | AGTCACATAGCTAGC[A/G]CCTTTATCCAAAGTT | 10451 |
rs371578808 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702915 | TATCCTCATAATAAT[C/T]GTCTAATTTACAAAA | 10451 |
rs371581967 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107849476 | AAAAAAAAACAATGG[A/G]GAAAGGATTCCCTAT | 10451 |
rs371607823 | snp | A/G | 1.65685e-05 | 0.00287819 | intron-variant | VAV3 | GRCh38.p7 | 1:107617655 | AAAAAAAAAAATGCC[A/G]GTGTTGAGAACAAAT | 10451 |
rs371630148 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662775 | GGTAGAAAAAGACAT[A/G]TTAGTCATATGAATA | 10451 |
rs371631410 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907301 | AAATTGTCTAGCACT[A/G]GGTGCTTATTTAATA | 10451 |
rs371641027 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107684578 | CTTGCAGGGTTCTCA[A/G]GTGAAAGCAAATTGG | 10451 |
rs371645679 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107882897 | ATTTTCATACTGATG[C/T]TAATATCACAGTAAA | 10451 |
rs371655950 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107637389 | GCACTTTGGGAGGCT[C/G]AGGAGGGCAGATCAC | 10451 |
rs371678088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921174 | ACTGCAATCCCATCC[A/G]CTCTCTCATCGCTTG | 10451 |
rs371692086 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107917462 | ATTGGTCTATCTGAC[C/T]CAGCTTACAGATCTG | 10451 |
rs371696775 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107637627 | ACAGAGCGAGACTCC[A/G]TCTCAAAATAAACAA | 10451 |
rs371696949 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107679784 | TCATGTTCTTGAAAA[A/C]GGCCTAGCACCTCCG | 10451 |
rs371717086 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107672464 | AATTAAACAATAAAA[G/T]TATAAGTAGGTGTTT | 10451 |
rs371740466 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107798307 | ATGCCTGTGTAAAAA[C/T]AGGAGGGGTGTTCTC | 10451 |
rs371744378 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107905821 | TTCTAAAAGAAAAAA[-/A]GTATTCTATTCTAGT | 10451 |
rs371746576 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107596925 | GTAATTCTTTCCAAT[A/T]TTCTCTTATAAATAA | 10451 |
rs371748511 | snp | C/G | 2.03996e-05 | 0.00319365 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964866 | ACTGCTTCCACGGCT[C/G]CATGCCCGACGGCTC | 10451 |
rs371750799 | snp | A/G | 1.91653e-05 | 0.00309553 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107602478 | TAACATTTTAGGAA[A/G] | 10451 |
rs371752476 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107615240 | TCCCTGTTCAGTAAA[C/G]GGGAGAAACAAGATT | 10451 |
rs371754128 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933814 | AAATGAGACCCTTCT[A/C]AAAAAAAAAAAAAAA | 10451 |
rs371761471 | snp | C/T | 1.65165e-05 | 0.00287367 | intron-variant | VAV3 | GRCh38.p7 | 1:107770632 | ATAATACCTGATGAC[C/T]TACCTTTTCTATTGA | 10451 |
rs371762178 | snp | C/T | | | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574089 | GCCATTTGCACTCAT[C/T]TTTGTGTAAATCTTC | 10451 |
rs371770141 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650784 | TCTCATTGTTCAATT[A/C]CCATCTATGAGTGAG | 10451 |
rs371774532 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107620374 | ATACCATACTTTTAC[C/T]GTACTTTTTCTATGT | 10451 |
rs371778470 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107783612 | TGGACATGTACCATC[C/T]TGAACCCAGTGAGGC | 10451 |
rs371799312 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107910992 | CAGTCTCATTAAAAG[-/A]AAAAAAAAAGAAAAA | 10451 |
rs371801720 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774810 | CAGCCCCAAAATTTA[A/G]AGTTAAGTATATTTA | 10451 |
rs371862699 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107629367 | GTAATATGAACAATT[C/T]CTTCCAGCATGAAGG | 10451 |
rs371876687 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921217 | GAAAGCCTGGCCTTA[-/A]GGATCTATGTATCCT | 10451 |
rs371885477 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107953948 | CTGAATACACTTCTT[G/T]TAACACAGATTTTGA | 10451 |
rs371888885 | snp | A/C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107672022 | CCTGTAATCCCAGCA[A/C/T]GCCGCAAGGCCAAGG | 10451 |
rs371895310 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107943094 | TCCTTTTTGACTTAG[C/T]TCTGATTCAATTCCT | 10451 |
rs371903182 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107765493 | TCCAAAAACAAAATT[A/G]AAAATTTCTGTTAAA | 10451 |
rs371905473 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107782556 | AACAAATATACAAAT[A/G]CAGCAAATGAGGAGG | 10451 |
rs371916008 | snp | C/T | 3.29609e-05 | 0.00405948 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107596261 | TGAATGTTCTGGCTC[C/T]TTGTATGGAAACTGC | 10451 |
rs371940012 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107642806 | AACAATGATGCATGA[A/C]GTCTACATGAACTTT | 10451 |
rs371942746 | in-del | -/GCGCGCGCGCGCGCGCAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575001 | TGTGTGTGCGTGCGT[-/GCGCGCGCGCGCGCGCAC]ACGCGCGCGTGTTTA | 10451 |
rs371965071 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107629537 | ACCTGCACTAGAAAA[C/T]GTGCCCCAAATGGCC | 10451 |
rs371970571 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107841803 | AAGTGTAAATACAAA[C/G]TGGGTTTGGAAGAAT | 10451 |
rs371972844 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662506 | TCCAGAGCACAAATG[C/T]TGCTGTTTTTCAATG | 10451 |
rs371979063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107833275 | TTTTCGTGGTCTGGA[C/T]AGATCAGATCAGCCA | 10451 |
rs371982588 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107699826 | TTCAAATACAGCATG[A/G]ACAAGTGGAGATTTA | 10451 |
rs371983653 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908962 | GCTACATAAGTACAA[C/T]AACTGCTATTCATAT | 10451 |
rs371985202 | snp | G/T | 0.000193609 | 0.00983702 | intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964641 | CTGCCGGCTGGAGGC[G/T]GGGCGCCCGTGCCGG | 10451 |
rs371987024 | in-del | -/CTC/CTCTG/CTTT/TCTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722841 | CCTATTATCCTCTCT[-/CTC/CTCTG/CTTT/TCTT]TTTTTTTTTTTTTTG | 10451 |
rs371992451 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951811 | TATTATCAAAAAGTC[-/A]AAAAAAAAAAACATG | 10451 |
rs371997979 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893621 | TATAAAACCATCAGA[C/T]CTCATGAGACTTATT | 10451 |
rs372001949 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107862918 | CTACCAGGGACCAAG[C/T]TTCCACTAGATAATC | 10451 |
rs372003040 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107747159 | TGCTGGGATTACAGG[C/T]ATGAACCATCACACC | 10451 |
rs372008126 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107885263 | TCGCTTTTATTTTTT[A/T]TTTTTATTTTTTTGA | 10451 |
rs372026126 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107637744 | AATAATGCTAATTCT[A/G]TAAATCTCTTTTAGA | 10451 |
rs372033225 | snp | A/G | 6.63009e-05 | 0.00575726 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107757304 | TTTGCCTTCTCAGTC[A/G]GATCAGTGGTATGTT | 10451 |
rs372050215 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107707473 | TTTGGTGTTCAATCA[A/G]TGTTGGCTACAATTT | 10451 |
rs372057818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107714149 | AAGCTGTCTGAACTA[C/G]AAATTGACCTTTTGA | 10451 |
rs372062192 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107910636 | ATGTAATACTAATAA[C/T]ATAAGGTTTTCTTCT | 10451 |
rs372063460 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757616 | GTTATGAAAGATTCC[A/G]TAATGATTAAAATCA | 10451 |
rs372081014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591087 | ATGCTTATGAACCTT[C/T]ACACAAACGACCTCT | 10451 |
rs372083220 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107626264 | TCAGTTTATGATCTA[C/T]TTAATCAAAGCCAGT | 10451 |
rs372087945 | snp | A/C/T | 4.44257e-05 | 0.00471284 | intron-variant | VAV3 | GRCh38.p7 | 1:107705113 | TTCACAACAAAGCTG[A/C/T]AATTTAGTCATCTAA | 10451 |
rs372088874 | snp | A/C | 0.0013356 | 0.0258073 | intron-variant | VAV3 | GRCh38.p7 | 1:107766591 | GAAAGTAGGAATAAC[A/C]ACCAAAAAATACACC | 10451 |
rs372114067 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107711691 | GAGAAATAAATGCAT[-/T]CAATAAATTCGTAAG | 10451 |
rs372116407 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107655621 | GCAAAAATAGAACAC[A/G]ATTACATTAAACTAA | 10451 |
rs372118352 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689713 | AACCTTTACAAAGGA[A/G]TATTCCTGGACAAAA | 10451 |
rs372123122 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107752618 | AAGACAAAAAACAAC[C/T]TGATTCAAAAATGGG | 10451 |
rs372138741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107573946 | GTGGGCTGAAAGCTG[C/T]AATACAGTATAGAGG | 10451 |
rs372162255 | in-del | -/TTAAG | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107872435 | TAGATATTATTCATT[-/TTAAG]TTAACAGAACATTTA | 10451 |
rs372162746 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107595738 | GTATGGTTTTAGAAA[C/T]ACTAGCATCCAAAAA | 10451 |
rs372165930 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107868857 | AGTGAAAACTGGCTC[-/A]AAAAAAGAGAAAAGG | 10451 |
rs372174840 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107806286 | GTGGAACATTTTCCA[C/T]GTGCTTGCTGCTGGG | 10451 |
rs372182045 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107837551 | ACCCTGAAATTCATA[C/T]GGAACCAAAAAAGAG | 10451 |
rs372183164 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107791364 | TAGATTAACTAAAAG[C/G]AAGTTTTTTTTGGTG | 10451 |
rs372197284 | snp | A/G | 7.32163e-05 | 0.00605002 | intron-variant | VAV3 | GRCh38.p7 | 1:107749101 | ATTAATATTCCTTAG[A/G]TTAATATGTATCATT | 10451 |
rs372198977 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107845206 | CCTGCAGCAGAGAGG[C/T]CTGACTGTGAGAAAG | 10451 |
rs372203124 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107861922 | TGCATACATACTTCA[A/G]TGGGGAGTGTTCTGA | 10451 |
rs372203314 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107712137 | TCTCTCTCACACGCA[C/T]ACTTATAAATATACA | 10451 |
rs372215262 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107812731 | TTAGGGGTCAAGCAC[C/T]AGGAATAGGATAAAA | 10451 |
rs372215715 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107766313 | CTACTCTGAAAGTAA[C/T]TGTCCCACGTTCTAA | 10451 |
rs372219643 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107827162 | CGACATTCAGTCAAG[G/T]GTCCTCTGAGCTAAA | 10451 |
rs372234029 | snp | C/T | 1.66192e-05 | 0.00288259 | synonymous-codon, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749534 | TATTATTTCCTTCAT[C/T]TCATAGTTATCACCT | 10451 |
rs372236899 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856560 | AACATTACTGTTATA[A/G]TAGTTAATTTAAATT | 10451 |
rs372237760 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107934451 | GGCTATGTGTATGTG[C/T]GTGTGCATCCTTCAT | 10451 |
rs372243932 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107631039 | CAATTAGAGAAGACT[A/G]TATCAAGTTCGGTAC | 10451 |
rs372254289 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107905080 | GGAGCCAAGGTGGCT[G/T]GAGAAGTCAGATTAT | 10451 |
rs372284227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788413 | GCTTTGCCTGCTGTG[C/T]TCCAGACAGACTCCA | 10451 |
rs372296423 | snp | C/T | 0.0618563 | 0.164627 | intron-variant | VAV3 | GRCh38.p7 | 1:107583513 | ATCTAGAAAACCCCA[C/T]TGTCTCAGCCCAAAA | 10451 |
rs372298821 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107627492 | TCTTCACATTAAATA[C/T]TGGGAAGAGGAAACC | 10451 |
rs372301007 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107614888 | TCAATGCTTAATATT[C/T]TTGATTTGATGTCTT | 10451 |
rs372310293 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107751133 | TTTCTTGTTTGGTAT[A/G]CTTGTCTAGAGTGGT | 10451 |
rs372311923 | in-del | -/GCTG | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107664049 | TAGTAAAATAGGACT[-/GCTG]GCTGGCTCATTAACA | 10451 |
rs372314733 | snp | A/C/G | 0.000664102 | 0.0182118 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964862 | GCGCACTGCTTCCAC[A/C/G]GCTCCATGCCCGACG | 10451 |
rs372317285 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925424 | AAAAGATTAAAGAAA[C/G]TCAAGTATTCATCAA | 10451 |
rs372324510 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676858 | ATTCATAACCTATAC[A/G]ACACACTTTGGTAGT | 10451 |
rs372326742 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728445 | ATAGTGGCATTTGAG[A/G]GAAAAATAATCTGTT | 10451 |
rs372342017 | in-del | -/TC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907673 | CTCGTGTGCGTGCGT[-/TC]TCTCTCTCTCTCACA | 10451 |
rs372413917 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847886 | AGCTATTCCAAATAA[A/T]AGAAAAAGAGAGACT | 10451 |
rs372417463 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107872294 | AAGCACTCTGAAAAC[G/T]TCAAAGGCTATAAAA | 10451 |
rs372431764 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107872960 | TTAGTACTGGTAAAT[C/T]ATGAAGCTATATCAC | 10451 |
rs372441741 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107711568 | AAATCCTTCTAAAGA[C/T]AGCAAATTCGAGCTT | 10451 |
rs372445365 | snp | A/C/T | 0.000431208 | 0.0146776 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874914 | ACCTTTCCAAAGTCA[A/C/T]GAACATCAAACAAGT | 10451 |
rs372490972 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624454 | TGATAGAAAAAAAAA[A/T]TTTGGCAACAAAAAC | 10451 |
rs372513864 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951440 | CTGTACAAATGTCTA[C/T]AGAGAGAAATACAAA | 10451 |
rs372519653 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107939857 | ATATCTCCCCCCACC[C/T]CCATGCACCAGAAAG | 10451 |
rs372527301 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720571 | TAATCCCAGCTACTC[A/G]AGAGGCTGAGGTAGG | 10451 |
rs372533839 | snp | A/C | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788545 | AAAAGCAAACTGGGA[A/C]CAGCAATACTAATTT | 10451 |
rs372535540 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107805821 | TAATTTACCTGTTAC[A/T]TTCTTTTTTCTTTGC | 10451 |
rs372539845 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107657057 | CTCCCGGGTTCAAAG[C/T]AATTGTCCTGTCTCA | 10451 |
rs372544079 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107742778 | TGAAACGACCTCAGA[A/T]TCTAACAGGCAGAGG | 10451 |
rs372556087 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107597855 | AACTGTAACAGCTAC[A/C]CCATTATCCCATGTG | 10451 |
rs372556560 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107577294 | GGTACCTGCTCTTAG[C/G]GACTGCTGCACTACT | 10451 |
rs372556948 | snp | A/G | 0.00184157 | 0.0302885 | intron-variant | VAV3 | GRCh38.p7 | 1:107603026 | GAAATCTATTTCTGT[A/G]AAAGTACTTGTCCTA | 10451 |
rs372561088 | snp | A/C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107664095 | TTCTTCTCTTTCTTA[A/C/G]TGGTTTAATAAGCAT | 10451 |
rs372566687 | snp | A/T | 3.31917e-05 | 0.00407367 | intron-variant | VAV3 | GRCh38.p7 | 1:107770740 | ATTTCTGCAGTTAGA[A/T]TTATCAAAATAAAAT | 10451 |
rs372568687 | snp | A/C/T | 0.000134394 | 0.00819636 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107704996 | TTGCAGGATGTGACT[A/C/T]GAGTGAAGGTATGCA | 10451 |
rs372589874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107721987 | GCAGATGAAGGCAAG[C/T]ATTAATGGAGCTAAC | 10451 |
rs372612339 | snp | A/C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107703322 | TGTTTCTGACTTTCC[A/C/G]ACAGAAGTAAGAGGT | 10451 |
rs372613287 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107750849 | CTGTTCTTACTTTAT[C/T]GCTCTTCTCATTTTA | 10451 |
rs372615951 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107883143 | TTAACAGGTTTTTTT[-/T]CACAGTATTCAATGA | 10451 |
rs372620937 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720018 | GAACAATGAGAACAC[G/T]TGGACACAAGGCAGG | 10451 |
rs372631783 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107780177 | TCTTCTAGATAATGC[C/T]TATAATAATAGTTAG | 10451 |
rs372640537 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107754611 | TTTAATAGCTTCCCA[C/T]TGCAGTCACAATAAA | 10451 |
rs372663867 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107823457 | GAAATGATAAGTGAA[A/G]CAATGGGAATGGCTG | 10451 |
rs372671367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107885238 | AGGGAAAAGGTGACA[C/T]ATAAGTCTGTCGCTT | 10451 |
rs372677804 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107824012 | GTATTTTGTTACGGC[A/C]GTCCAAACAGACTCA | 10451 |
rs372685094 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107613935 | AATCTGGAATAATTT[A/T]AAACTACACTTCTAG | 10451 |
rs372688784 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902504 | TGCCCTTTCACTATT[A/G]CCATGCACCTAAGTA | 10451 |
rs372709864 | in-del | -/GGGGG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889584 | TATACTATTATGGCT[-/GGGGG]GTTTAAAAATCACAT | 10451 |
rs372720743 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964206 | GCCCTTCACTTCCTC[A/G]AGTCCTCATGTATGT | 10451 |
rs372728140 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107647295 | ATTTAAAATCTAAAC[A/C]CAGCCACATTAAAAA | 10451 |
rs372748853 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107802064 | TTTACATTATACAGA[C/T]CTTCCACTTCTTTAA | 10451 |
rs372756699 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107667016 | GCAGCTTGTACTGCT[A/G]CCTCTGCTCTAATGG | 10451 |
rs372763156 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628030 | ACCCTTAGGACACAG[C/T]ATGATGGGTGTTATG | 10451 |
rs372779863 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107801640 | ATAAGGCAAACACCA[A/G]CCTGTAACCAATCCA | 10451 |
rs372780249 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107905975 | GAAGAGTCTATTAAA[C/T]AAGGTCAGAAGCAAA | 10451 |
rs372781504 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107939100 | CTGGTTCTGGGGGCT[A/G]CCCAATTTGCAAATC | 10451 |
rs372789243 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107958266 | CTCCTTCCCTTTTGT[A/G]TAACCCAAAAATCTG | 10451 |
rs372815488 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632603 | CTGTATGGGAAACAC[C/T]AGATGAACTTTAAAT | 10451 |
rs372816729 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107716366 | GGTGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA | 10451 |
rs372824264 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107865180 | AGTTTTACTTGATCT[C/T]AAAGTCTCAGGATGA | 10451 |
rs372830123 | snp | C/G | 0.0629771 | 0.165899 | intron-variant | VAV3 | GRCh38.p7 | 1:107737717 | ACAACAGGTGCTGGA[C/G]AGGATGTGGAGAAAT | 10451 |
rs372833953 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107843615 | GAAGTATGAGCAGGC[A/G]TATTTAAACCTCCAC | 10451 |
rs372837070 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107895113 | TCCAAGTCAGTTTGG[A/G]ACGAAGAGGAAAAAA | 10451 |
rs372841949 | in-del | -/A | | | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587424 | TTTTTAGGAAGAAAA[-/A]CTGGGAATTTCTCCC | 10451 |
rs372843076 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929288 | GTGACACTCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10451 |
rs372850551 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920040 | TTTCATAATGTCTGA[A/C]CTTATCTCCTTATTA | 10451 |
rs372853812 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733635 | CAAGTGGAAGAAAGG[A/G]TATAAATGAGTGAAG | 10451 |
rs372863876 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107836313 | AAATTCAAACAACTT[A/C]CTCCTGAATGATTTT | 10451 |
rs372878037 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107615828 | GACATACATATAATT[C/G]GCCAAAAAAAATTTG | 10451 |
rs372885929 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951589 | CTGACAAAGGCCTAA[C/T]ATCCAGCATCTATAA | 10451 |
rs372888270 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107631747 | GTTTTTTGTCCTTGC[A/G]ATAATTTGCTGAGAA | 10451 |
rs372892044 | snp | A/G | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570785 | ATCGCCTGTCCATTC[A/G]GAATGGCGCTCACCT | 10451 |
rs372908741 | snp | A/G/T | 1.64879e-05 | 0.00287118 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107603127 | CCTATTAATAAGTTC[A/G/T]GTCTCTGCTTGCAAT | 10451 |
rs372913766 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874901 | ATGAAGTATAATTAC[C/T]TTTCCAAAGTCACGA | 10451 |
rs372919907 | snp | C/G/T | 0.000123947 | 0.0078715 | utr-variant-5-prime, intron-variant | VAV3 | GRCh38.p7 | 1:107688437 | AAATTGGCATTGTCA[C/G/T]TGTAAAGTTATTTTG | 10451 |
rs372926914 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107757249 | AACAAATTACTGATG[A/C]ATCTGCCCTACCTTC | 10451 |
rs372933985 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107574511 | AAATTAAAAAAACTC[A/G]TTAATATCTAAGTAT | 10451 |
rs372977055 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107862060 | CTTTTCATGTCCAAA[A/G]AGCATTATAATTGGC | 10451 |
rs373004339 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107652117 | CGCTAGGAGGTCAGC[A/G]CAAGATACAGGTCAT | 10451 |
rs373017260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107708394 | TAACATATGACAATT[C/T]ACTTTTGAGAATGTC | 10451 |
rs373022324 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107605630 | AAAATCTGAAACTTT[C/T]TGAGAGTCAGCATGT | 10451 |
rs373032785 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954776 | CCATGGGAGGGGGGG[A/G]AATTCATTGCAGTCC | 10451 |
rs373051319 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107638149 | TCTAAGATCTGGAAT[A/G]AGGCAAGGATATACT | 10451 |
rs373067619 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947683 | CTGGCCAATGCTAAA[A/G]TCCATATTCTTTCAA | 10451 |
rs373070540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107944595 | TCTGAATGAACAAAA[C/T]GCAGTTTTTTGTTTG | 10451 |
rs373074716 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107664960 | TGTGGAAAATTACCA[G/T]ATCTCTGCTATTGCA | 10451 |
rs373098063 | snp | C/T | 1.75634e-05 | 0.00296334 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755416 | AGCTGGATGGAAAGA[C/T]AATTACATACCAAAT | 10451 |
rs373102884 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107598514 | ATCTATAACTTGAAA[A/G]ATATGTATTTCTTCC | 10451 |
rs373120945 | in-del | -/ACA | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107731987 | ATATACACTTAACTT[-/ACA]ACAACTTACTTCTAA | 10451 |
rs373130917 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107672827 | ACTACTATGATATGA[C/T]AGTAAGATACTATTA | 10451 |
rs373145745 | in-del | -/AAAA | 0.0209274 | 0.100129 | intron-variant | VAV3 | GRCh38.p7 | 1:107649071 | AAAAAACAAACAAAC[-/AAAA]AAAAAGCAAGCACTG | 10451 |
rs373146295 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107776657 | GATTCTTTGCAAACA[C/T]GCCTGATCCATGTCA | 10451 |
rs373147288 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723147 | TCCTCATAAATGGTA[C/T]TCCACATATAATAGA | 10451 |
rs373155255 | in-del | -/GAAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107841306 | GGGGGGGTAGAAAAA[-/GAAA]CAATTTTAAAAGTAT | 10451 |
rs373159780 | in-del | -/CTAAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940706 | CTTCAGGACATTAAA[-/CTAAA]TAAAATAAGCTAGTC | 10451 |
rs373161072 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107955394 | GATGAATTTAATCTA[A/T]GCCTATTTATGTATG | 10451 |
rs373174345 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107894359 | AGGCAGAAATTTAAA[C/T]TGGCATCAACTCATT | 10451 |
rs373186470 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662742 | GCTAACGAAAGCACA[A/C]TTTCTGTGGGCCTAA | 10451 |
rs373194625 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107897884 | TAAAATCCCCTCTTG[C/T]TCTTTTCCCTACACT | 10451 |
rs373200381 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857493 | TTATAACTTTTTAGA[C/T]TGTAGTAACATTTTC | 10451 |
rs373203296 | snp | C/T | 1.66114e-05 | 0.00288192 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107765172 | CTGCCCGTAAATAAC[C/T]AATCTGAAAGGGAAA | 10451 |
rs373204433 | snp | A/C/G | 4.91464e-05 | 0.00495694 | utr-variant-5-prime, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964881 | CCATGCCCGACGGCT[A/C/G]CGGGACGCGGCTGGG | 10451 |
rs373206421 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580502 | ATGCCTGAGGAATCT[C/T]CTTAGGAGTAAAAGG | 10451 |
rs373209423 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940845 | TTGTTGTTTAATGTA[C/T]AGAGTTTCAGTTGGG | 10451 |
rs373215546 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107942484 | TTTCAGATCTTGTCT[C/G]ACTTCTTCAGGCCCA | 10451 |
rs373216758 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107784938 | TACTCAAACCTAGAG[C/G]CAACAAACATACTGA | 10451 |
rs373217624 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107627375 | TTTTATGTCTAATTA[C/T]GAAGTAAAAGTTTAA | 10451 |
rs373218825 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107797925 | TTGTACTTCTAGCAA[C/G]TTCTCAGAAGCTGTT | 10451 |
rs373219938 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107659769 | TTGGTTTTTGTTGAA[A/G]GCTTCTTTTTATACA | 10451 |
rs373232457 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922896 | GGCGGAGCTTGCAGT[A/G]AGCCGAGATCGCGCC | 10451 |
rs373232715 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107600832 | GGCCCTTTTCAGTGA[C/T]GATTCCTTTCATCTT | 10451 |
rs373234437 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107705417 | CCTTGTCTGTAGCCA[C/T]GCCACTGAAATATAA | 10451 |
rs373254301 | snp | A/C | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107668954 | TATTTGAATTCTCTT[A/C]AACTCTTTCGCGATA | 10451 |
rs373258809 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107829037 | CACATAACAAATTAC[A/G]GATGCTGGAAAGCAG | 10451 |
rs373264444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107852370 | AGGAAGACAAAGTCA[C/T]TGCATACAAAAATTT | 10451 |
rs373319358 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907685 | CTCTCACACACACAC[A/G]CGCTCTCTCTCTCTC | 10451 |
rs373320257 | in-del | -/TACTGG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772911 | TAGCTACAAATAGCC[-/TACTGG]ATTTTAGTAAAAAAT | 10451 |
rs373321147 | snp | A/T | 6.61266e-05 | 0.00574969 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107768441 | CATATTTTTACTCAC[A/T]GGAATGTTGATGAAT | 10451 |
rs373328277 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107774941 | TTTAAGATAACCCTA[C/T]TTCACCTTTTATCCC | 10451 |
rs373339281 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107690809 | CCTTTCTCCTTGCTA[G/T]CCCTTCCTGTCCTCA | 10451 |
rs373353234 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107630197 | TATCCTGAGTTCTGA[C/T]CATTCCTTACATCAT | 10451 |
rs373365291 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107961101 | CCAAGTAAATATTCA[C/T]TGAAGGAATCCTTGA | 10451 |
rs373369490 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847582 | ATAAAAAATGATAAA[C/G]GGGATATCACCACTG | 10451 |
rs373393039 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933203 | TTGTGGTTATTTTAT[C/T]GTCTTGTTTTGCTTA | 10451 |
rs373397736 | snp | A/G/T | 7.38791e-05 | 0.00607743 | intron-variant | VAV3 | GRCh38.p7 | 1:107785440 | TTCAAAAGGAATTCC[A/G/T]AGGGAAAGGGTACTT | 10451 |
rs373405433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597947 | TCCCATTGAAGCTCA[A/G]ATATCAGTGAGGTGA | 10451 |
rs373428574 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925471 | CAAAATATGGTGTAT[A/G]CATACAATGGACTAT | 10451 |
rs373443694 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107749872 | GAGTTGTTGAAAGGG[C/T]CAAGTGAGATAAGCC | 10451 |
rs373449216 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107633910 | GAGACCTTACAGCTG[C/T]TCCCACCACCCCAAC | 10451 |
rs373459009 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107651923 | CTTGTTCCAGCCTCA[C/T]ACTTGCTCACTCTTT | 10451 |
rs373461474 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769621 | AATTCAGTCTTTCCC[C/G]TTAATGCCTGATTCA | 10451 |
rs373470739 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107784120 | TCAGGCTGAAATAAT[A/G]CAGTAATACATAAAA | 10451 |
rs373473149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107721565 | ACACATCAGACACTT[C/T]GGAAGGAAAGAAACA | 10451 |
rs373475535 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632101 | TCCCACCAACAGTGT[A/T]AAAGTGTAACACCTT | 10451 |
rs373482800 | snp | A/G | 0.000153988 | 0.00877328 | missense, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107751186 | TGAGGTCGTCCAAAA[A/G]GCAAAACTGGTTGGT | 10451 |
rs373487801 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724354 | TGATCTGTCCTTTCT[C/G]TGAAGTTATATGGCA | 10451 |
rs373492477 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107777198 | ACACATAAATTGGCA[A/G]TGGCTAAATTTTGCT | 10451 |
rs373492496 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107789581 | TTTCATACACTGCTT[C/G]AAAGTGTTCATTTTC | 10451 |
rs373511548 | in-del | C/TT | | | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897636 | CCTCAGGTGCATTCA[C/TT]CCTGCCCATGACACC | 10451 |
rs373556583 | snp | C/T | 0.00118441 | 0.0243065 | intron-variant | VAV3 | GRCh38.p7 | 1:107748955 | AAGCACTTTTAAAAA[C/T]AGAAATACTCACAAA | 10451 |
rs373562398 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107717833 | GTCTAATATTGACAA[A/T]GGGGTGTTAAAGTTT | 10451 |
rs373564186 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107876820 | TTATACCAAAATAAA[G/T]TTTAAAAAAATGGAA | 10451 |
rs373579542 | snp | A/T | 6.61463e-05 | 0.00575055 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573281 | TGTGCAGGCTTCTAT[A/T]TATCCCTTCTCTGAA | 10451 |
rs373584427 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107681913 | GATCCGCCGGCCTTG[A/G]CCTCCCAAAGTGCTG | 10451 |
rs373590935 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107714060 | ATAGATGTTCACTTA[C/T]ACGCATTATTTTTCC | 10451 |
rs373592230 | snp | A/G | 6.5912e-05 | 0.00574035 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107772825 | ATAGAGATCTTCTTC[A/G]TCTTCCACAAGGGTT | 10451 |
rs373604483 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902736 | TGTATCAACAAGAGA[C/G]GGGAAGGAGAGCGAA | 10451 |
rs373618755 | snp | A/G | | | intron-variant, upstream-variant-2KB, utr-variant-5-prime | VAV3 | GRCh38.p7 | 1:107786630 | ATCCTCATCATCATC[A/G]GTAAAGTCAGATTTG | 10451 |
rs373625552 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107722950 | CCAGCTCAAATGTTA[C/T]CTCCTCTGAGAAGCC | 10451 |
rs373647624 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966690 | GACAAGGATAGCACA[C/G/T]TGTTTACACTCAGCG | 10451 |
rs373669905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594875 | TAAGTGAACAACTCA[A/G]ACAGGATTTTTCATC | 10451 |
rs373672871 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628769 | AGGGGACCACAAGTC[G/T]GAAAAGGACTCTAGT | 10451 |
rs373675100 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572544 | TACCTAGCCCAGATC[A/C]TTTCATAAAGTCAAG | 10451 |
rs373676319 | snp | A/C/T | 1.66106e-05 | 0.00288184 | missense, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749547 | ATTTCATAGTTATCA[A/C/T]CTTTTCTCTTACATA | 10451 |
rs373685650 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107645834 | AGGTTTTCTTCTCCC[C/G]TTAGAAAATATGCCT | 10451 |
rs373690145 | snp | A/G | 0.000652681 | 0.0180531 | intron-variant | VAV3 | GRCh38.p7 | 1:107574036 | CCAGCACATCGAGAG[A/G]GCCAACTTACCCTGC | 10451 |
rs373691277 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107949717 | ATTGCTATATTTTAC[A/G]GAATCCCAAAGTACA | 10451 |
rs373697550 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693686 | TTCTGGTTGAAATAG[C/T]CCTATTATGGGAAAA | 10451 |
rs373726784 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107612492 | TTCATTATGAACATG[C/T]TTTCCTTTGTGTCCT | 10451 |
rs373727107 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871759 | CCATATCAAGCCTAA[A/G]ATTCAAAATAAATCT | 10451 |
rs373735946 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572415 | GGAGGTGGATGGGAG[-/G]AAAAGGCATGTATTA | 10451 |
rs373737009 | in-del | -/ACAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952486 | TATATATATATATAT[-/ACAC]ACATAAATTCAACCT | 10451 |
rs373740907 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107724864 | CTAGAGCTGAGCACA[A/G]GCCAGATAGTAAATG | 10451 |
rs373761719 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107691437 | GCCTTAGTTCTGCAA[C/T]AGAGCTGAGATAATT | 10451 |
rs373772673 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107608343 | TTTGTAACTATAATG[C/G]CCAGTTACATGAAAA | 10451 |
rs373782279 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107783081 | GGTGAGTAAGAAGAG[C/T]GGCATCTGTAAAGAA | 10451 |
rs373785520 | snp | C/T | | | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587707 | GCAATTCTTCTGCCT[C/T]GGCCTCCCGAGTAGC | 10451 |
rs373794733 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107623760 | ACCATAAGCTATGCA[-/T]TTTTGTTATTTCTTA | 10451 |
rs373796150 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107751756 | CGAAAAGCTCTGAGT[A/T]AATTATTTAAAATAA | 10451 |
rs373799659 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107640103 | TATGATCTATATATT[A/C]CCCTCTTGGCATTAG | 10451 |
rs373811683 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107699033 | TATCATTCTGCTCCT[A/G]GCCCCTCCCAAAACT | 10451 |
rs373814467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657067 | CAAAGCAATTGTCCT[C/G]TCTCAGCCTCCGAAG | 10451 |
rs373814995 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107843755 | GATAAAATCAGACAC[-/G]GAAAAATGCATTTTT | 10451 |
rs373818191 | snp | A/C | 0.000437904 | 0.0147905 | intron-variant | VAV3 | GRCh38.p7 | 1:107617511 | GATTTTTGCACAATT[A/C]ATCACAGGATCAAAA | 10451 |
rs373818515 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673203 | CTCAAGATTCAAGTG[C/T]GGCTAGGGTGATCTT | 10451 |
rs373828585 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921819 | CATTAAATATATCGT[G/T]TTGATTTTCTTAATC | 10451 |
rs373838570 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693795 | TCCGAACAGCAAAGG[A/C]GCATATAATCTAACA | 10451 |
rs373842683 | in-del | -/ACACACACACACACAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908821 | CCCCGCCCCACTCAA[-/ACACACACACACACAC]ACACACACACACACA | 10451 |
rs373844422 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962802 | AACTCAAAAGTGCAA[C/T]GGCACAAAGAAGGTC | 10451 |
rs373845048 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662418 | TAAGGGAAAAAAAAA[C/T]ATCTGCCTCAAGTGG | 10451 |
rs373851532 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107718613 | GGAAGAATCAATATC[A/G]TGAAAATGGCCATAC | 10451 |
rs373868759 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107805654 | CTGTTTCATTAGGTT[A/T]GGTCACTGGTTCCCT | 10451 |
rs373869418 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107677210 | CTTGCTATTTCTACA[C/T]AGAACTGTAGTATAA | 10451 |
rs373896153 | in-del | -/TTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918706 | ATATATATATATATA[-/TTT]TTTTTTTTTTTTGAG | 10451 |
rs373896211 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | VAV3 | GRCh38.p7 | 1:107629124 | GAACATTTGGATATT[C/T]GTAAATGACAATGGA | 10451 |
rs373902752 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710278 | AGTATGGACATTGTG[G/T]CAATTATGTAGTATA | 10451 |
rs373908081 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107683450 | TCATAAGCACTTAGC[C/T]GAAGCCATAATTATG | 10451 |
rs373915183 | in-del | -/TAAGGGTCCTACAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951095 | CAGTACTAATGTTAT[-/TAAGGGTCCTACAT]CATCGTTCAGAATAG | 10451 |
rs373915330 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107677132 | AACTAATTGCCAATA[-/T]GAGTCATTTTGACAG | 10451 |
rs373933372 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713480 | CCATAAGAAAAAAAT[A/G]AACATCCCAATTGGA | 10451 |
rs373941550 | snp | A/C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107770289 | ACCAGCCCTCCCCCC[A/C/G/T]CATCACTCTCTATCT | 10451 |
rs373955513 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107736610 | CCATTCACAATTGCT[A/T]CAAAGAGAATAAAAT | 10451 |
rs373958365 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788620 | GTTTTACCATCCCCC[A/G]GTCCAAATAGCAAAG | 10451 |
rs373967783 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107759082 | GGTTCTGTACCTTAC[A/C]TGTACCTATCATATT | 10451 |
rs373971829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773922 | TCATTTCCCTGGCAC[C/T]CCTAATCCCAGAACT | 10451 |
rs373977600 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107725176 | TCTTACAACAGTCAG[C/T]TGGGAGTCAGGTGGC | 10451 |
rs373981989 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736072 | GCAAATGAATAAACA[C/T]AATTCATCACATAAA | 10451 |
rs373988860 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107915957 | ATCACAAAAAAAAAA[-/A]GGAAGCACAGGGGAT | 10451 |
rs373990124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750079 | GCTGGGAAGGTATCA[C/T]TGCCATCTTCATTTT | 10451 |
rs373991651 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921271 | CTGATCCACCAGGCT[A/G]ATTGCCAGGTATCAA | 10451 |
rs374015352 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107863571 | GCTTGCCCCTGTTGC[A/G]TCTTACACTCAAGCT | 10451 |
rs374018292 | snp | A/C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107835359 | CAGGCTTGTGGCAAC[A/C/T]CCCCAGGTTAGAGCA | 10451 |
rs374073483 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694189 | ATAGAAATAATTAGA[A/G]AACAATTTAATTCAG | 10451 |
rs374078467 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733324 | CTAAAAACCAGAGGG[C/G]CTCTTCTCCTCCAAA | 10451 |
rs374099833 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649536 | GCACTGAGGTCCAGA[A/G]TGATTATTGAGATGA | 10451 |
rs374106234 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107870355 | AAGGTGGTATTCCAT[C/T]GTGGTTTTGATTTGC | 10451 |
rs374121013 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658236 | AATTTGCTGAGAATG[A/T]TGGTCTCCAGCTTCA | 10451 |
rs374127110 | in-del | -/TCT/TCTCT/TCTT/TTT/TTTTT | 0.261884 | 0.249717 | intron-variant | VAV3 | GRCh38.p7 | 1:107722840 | CCCTATTATCCTCTC[-/TCT/TCTCT/TCTT/TTT/TTTTT]TTTTTTTTTTTTTTT | 10451 |
rs374136356 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107715453 | AATAAATTGAGATAA[A/T]GCTTTTCTTGTATTA | 10451 |
rs374140612 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107765957 | ACTCCAATTCCTATA[A/G]GTTGTCAGGAGATTT | 10451 |
rs374141055 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107820279 | AGTACTATTCGTCCA[C/T]AAAAAAATGATGAAT | 10451 |
rs374148733 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107808980 | CAATCGATGAAGGCA[C/T]TTTTTATAACTTCCC | 10451 |
rs374148954 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722838 | AAGCCCTATTATCCT[C/T]TCTTTTTTTTTTTTT | 10451 |
rs374157293 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625271 | TTTTTTTTTTTTTTT[-/C]TTTTTGGGACGGCAT | 10451 |
rs374158309 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107797054 | AAATTACTACAATAT[G/T]TAAGAAGTTACTATT | 10451 |
rs374158815 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107783803 | CCTGTAATCCCAGCA[C/T]TTTGGGAGGCTGAGG | 10451 |
rs374164400 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107782959 | GAGATACATTAACTC[C/G]CAGAAACAGACATAG | 10451 |
rs374166138 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833446 | CTTCATAACATAATT[G/T]TAAAATGATGTTAGA | 10451 |
rs374187237 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107751686 | GGGCGGGGGGGCGCG[C/T]GCTAATTTGGTCTAT | 10451 |
rs374189962 | snp | G/T | 3.30863e-05 | 0.00406719 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874969 | TCCTCATTCCAAACG[G/T]CTCACAACAGGCCGT | 10451 |
rs374206803 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107885533 | TGGGAGAACATGGAA[C/T]AGTCAAGCATAACAA | 10451 |
rs374237529 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107666872 | AGGTACAGAGGGTTT[A/T]AGTGACTTGAGCAAG | 10451 |
rs374251192 | snp | A/G | 3.30126e-05 | 0.00406266 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107642726 | GTGGTGTTCCAGAAT[A/G]GTTCCTAATGACCTG | 10451 |
rs374264750 | in-del | -/ATTAA | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896384 | GTCCTCTTTCATCAA[-/ATTAA]TCGCACAGCAGCCAT | 10451 |
rs374275983 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753304 | GTTTCCAGGGGCCAG[A/G]GAAAGAGAAGAATGG | 10451 |
rs374282558 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107586302 | TTTTAACAGTGCCTG[C/T]CCTGAAGTAGGCTCT | 10451 |
rs374298168 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107834529 | ACAATAGCAGAATAC[A/G]CATTCTGATCAAGCT | 10451 |
rs374304152 | in-del | -/ATATT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858369 | GAAATTTTAACTATT[-/ATATT]TCTTAGAACCAAAAT | 10451 |
rs374329556 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582412 | TGCTTATTGTATATA[C/T]ATATTTTTTATTATT | 10451 |
rs374329940 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107820609 | AAAAAATAACTAAAA[A/G]TATAATTGGAATATT | 10451 |
rs374342439 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840698 | TCAAGGCAGGAAAGG[A/C]AAAAAAGTGACTAGG | 10451 |
rs374349201 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769747 | CTTCCCCACCCCTGT[A/C]ATCTTCACCATTCAT | 10451 |
rs374350748 | snp | A/G | 3.53863e-05 | 0.00420618 | intron-variant | VAV3 | GRCh38.p7 | 1:107749445 | TAAATTACAGTTATT[A/G]GTTTCCAAAAAGTCA | 10451 |
rs374359300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107932612 | TTATGGTAAAAGGGA[C/T]TTTGCAGACATAATT | 10451 |
rs374362984 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871958 | CATGCAGTATCCTAA[A/T]TCTTTCCTTTCTTTC | 10451 |
rs374390287 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107709991 | TTTCAGTAATAAGTA[C/T]GACAGTGTAGTTAGT | 10451 |
rs374391649 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107819910 | AAACTACAGTGAAAT[A/G]TCATCTCTACCCCGT | 10451 |
rs374408802 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107837461 | AAATGGCCATACTGT[C/T]CAAAGCAATTTACAG | 10451 |
rs374410905 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107735585 | TATAAACACCTCTAC[A/G]CAAATAAACTAGAAA | 10451 |
rs374439941 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | VAV3 | GRCh38.p7 | 1:107574234 | ATGACAGTAGGTTTG[C/T]AGTTCGTTAACAACC | 10451 |
rs374442677 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920895 | ACAAAAGCCTTATTT[A/T]TACTTTATTCTCTTC | 10451 |
rs374445661 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722924 | GAGAATTCCTGTTCA[G/T]TCTTGAGGACCCAGC | 10451 |
rs374447040 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107886625 | GGTTTTGTATAGTGG[G/T]TAGTTTCCAAAATAG | 10451 |
rs374456031 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858305 | TTATACAAGATTTTC[C/T]AAAAACAGTTTCTTC | 10451 |
rs374461518 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107576278 | GTGGTAATGGAACTC[A/G]AGGGATTGTCTGTGA | 10451 |
rs374462538 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898464 | TCTGAGTGAAGCATG[A/G]TTTTCTGCCCTACAT | 10451 |
rs374514476 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107770084 | ATGCTCAGTCCCCTT[A/C]CCTCATTCTGCTCCA | 10451 |
rs374529383 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107599843 | CCAATAACAAGAGGA[G/T]ACTGAACTATTCTTA | 10451 |
rs374545999 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572199 | CCTCCAGTTAATACA[C/T]TCCCAGGATGGGCTG | 10451 |
rs374552299 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107927202 | CCTGGGCCACAAGGG[-/A]ACCCACTGCCATGAA | 10451 |
rs374560090 | snp | A/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592560 | GCAAAATATTTAAGG[A/T]CTGCTTATGGGTCAC | 10451 |
rs374565316 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107667794 | TCCTGATATTTTGCT[A/G]TGATTTTATTTTCTA | 10451 |
rs374566042 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107737721 | CAGGTGCTGGACAGG[A/G]TGTGGAGAAATAGGA | 10451 |
rs374566306 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107891787 | GAGGTTGCAGTGTGC[A/G]GAGACCGCGCCATTG | 10451 |
rs374591486 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753529 | ATATATATATATACG[C/T]ATATATATATATATA | 10451 |
rs374622644 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923233 | TTTGGGTTTTGTTTT[A/G]GAATTGCTTAACCCC | 10451 |
rs374638919 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107791356 | CAGTTCAATAGATTA[A/T]CTAAAAGGAAGTTTT | 10451 |
rs374653386 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107852054 | CAGAGGTACAATTAA[A/G]TTATCATACCTCCAA | 10451 |
rs374676365 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107851472 | TTTACCTTTAATCTT[A/C]AATGTTCTTGCCTAT | 10451 |
rs374683501 | in-del | -/GGGGGCGG/GGGGGCGGG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954764 | ACAGGAAAATACCAT[-/GGGGGCGG/GGGGGCGGG]GGGAGGGGGGGAAAT | 10451 |
rs374691969 | snp | G/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756391 | TTTTCATAGGATAGA[G/T]CCATAAACGACTTCT | 10451 |
rs374696123 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107943598 | AGTACAAAAATTAGC[C/T]GGGCATGGTGGCACA | 10451 |
rs374701535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875425 | TCTCACAGAGAAGAG[A/G]ATGGTGGAGCAGAGA | 10451 |
rs374707741 | in-del | -/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590876 | TAGCCTCCTAACTCA[-/T]CTTCCCTCTGTGCAT | 10451 |
rs374712107 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107924213 | TGTCAACAACCCATT[A/G]CAGTTTTGAAGGCAA | 10451 |
rs374713974 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925881 | CAGATATGTCACATA[C/T]AAATATATAACATAT | 10451 |
rs374718001 | in-del | -/GTTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107876947 | TGTTTATCTTGGTTT[-/GTTT]TTTTAATTTGCAGAA | 10451 |
rs374724238 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107788791 | TAGTACACAACCGTA[A/G]AAGAAACACTTTCAT | 10451 |
rs374724964 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662867 | TTTCACAATGGGGCA[C/G]GTGTCAATCAGAAAG | 10451 |
rs374732419 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893359 | ATAATAAAAATCACA[C/G]GGTAAAAGTGTTTAC | 10451 |
rs374741108 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107678863 | TTATTAAACAATTCA[C/T]TAATTGTTTTTAAGA | 10451 |
rs374741440 | snp | C/T | 0.000676404 | 0.0183778 | intron-variant | VAV3 | GRCh38.p7 | 1:107602506 | GCAATGAATAACTTA[C/T]GAATATAAATGTGTT | 10451 |
rs374746554 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871540 | GCGTTTCAAACTGTT[C/T]TAATTTTTGTTGATG | 10451 |
rs374750205 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107576317 | ATCCGTATGAGAAGC[C/T]ATACATGGAACTCAA | 10451 |
rs374750391 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107776921 | CCCACAACTCCAGCA[A/G]CAGATTCTATTTCTT | 10451 |
rs374752928 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | VAV3 | GRCh38.p7 | 1:107709375 | AAGCTGCCTTTTGCC[A/G]CATTATCAGATAGAA | 10451 |
rs374758370 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922223 | TCCACATCAAGCTGT[A/G]TCATAATATATATTT | 10451 |
rs374761590 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107815694 | TGGAATGAAATTCAA[C/G]CACTATCAATAATTA | 10451 |
rs374792153 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856259 | AATGTGATTAATTAC[A/G]GTTTACATCATTCCA | 10451 |
rs374797006 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107877060 | CCCTTCACGGGAATC[A/C]TTCTCAGAGGCTTAA | 10451 |
rs374797374 | in-del | -/CTC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107763022 | GAAAAAGACAAAAAA[-/CTC]AACAAGAACAAAAAT | 10451 |
rs374819145 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574133 | TCAACAAGGACAACT[C/G]TCTCATATCTCTTGC | 10451 |
rs374835069 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963257 | GAGGCTACAGGCAAA[A/G]TGGAAAATGGGGATG | 10451 |
rs374837857 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107930264 | ATTACACATTGCATG[A/C]CTATATCAAAATATC | 10451 |
rs374841125 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107914317 | CTCGCAACAGTGACG[C/T]GCAATAAACATTACT | 10451 |
rs374849895 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107694968 | CCCAGGCATTAGGAG[G/T]GTCAGAAAAGGTTTT | 10451 |
rs374851696 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107637673 | AAACCTTCCACTAAG[G/T]AAACTCTAGGCCTAG | 10451 |
rs374852024 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107605866 | ATTCAAAACACTTCC[A/G]GTCCCAAGCATTTTG | 10451 |
rs374857795 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624741 | CAGCATGAGATATTT[C/T]TAAAGAATGTTACTT | 10451 |
rs374863989 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107605438 | TGATATCTCCTGCCA[G/T]GTTATTATGCAATGA | 10451 |
rs374880335 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723276 | GCCACAAGCATTCAG[C/T]GCCCATCTGATGTCA | 10451 |
rs374888031 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107584592 | ATATTTTATATATTG[C/T]CACTGAAAAAAAACT | 10451 |
rs374892475 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107635755 | ATCCCTAAGGTGCAT[A/G]AAGTTTAGGAAGGCA | 10451 |
rs374895635 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107574276 | ATCAGATGAATGTTA[C/T]TGATGCTATCAAATG | 10451 |
rs374908097 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107854083 | GGAGGCTGACACCAG[C/T]AGATAACTTGAGGCC | 10451 |
rs374920432 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107789571 | ACAGTGGTCATTTCA[C/T]ACACTGCTTGAAAGT | 10451 |
rs374927531 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107719744 | AAATCATGCTACTAT[A/C]AAGACACATGAACAC | 10451 |
rs374931302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107799723 | ATTCTCTTCCAGCCA[C/T]CTTGAAATGTACATA | 10451 |
rs374932430 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757777 | TCCTAAATTTCTGCC[A/T]CCTCCTCAGTCTTTC | 10451 |
rs374949913 | snp | C/T | 3.29946e-05 | 0.00406155 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107770660 | TGACTCCAAAGTTTC[C/T]GTATATTTTTCTTCT | 10451 |
rs374954831 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628658 | TACCAAAAAATAACA[A/T]AACTGCCTTTAAAAG | 10451 |
rs374967904 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590668 | TTCTGTTTCCTGGAT[C/T]GTTAATGGTTTTATC | 10451 |
rs374979783 | in-del | -/AAAT | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107889629 | AGATTTTACATAAAC[-/AAAT]AAAACCCTACACCAC | 10451 |
rs374991729 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945895 | AGGATAAGATGTATA[C/T]AAGGGGTATTTGGAA | 10451 |
rs375014233 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107825039 | CTGTCTTAACATTTT[A/G]TAAATAAAGTTTTAT | 10451 |
rs375025539 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947524 | TGCTGTGCTAGGTAT[C/T]TTGCCCATCTGAGTT | 10451 |
rs375038342 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107626217 | CCAATTCCCATACTA[C/T]AGTCTGTACACTTGG | 10451 |
rs375051069 | snp | A/G | 3.3749e-05 | 0.00410772 | intron-variant | VAV3 | GRCh38.p7 | 1:107874865 | GCTTAAATGCTTTCC[A/G]GTTAAAAAGTAGTGT | 10451 |
rs375052354 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107897029 | CAAAGAAATCCACAG[C/T]CCACAATAAGGTTTA | 10451 |
rs375088872 | in-del | -/TT/TTT/TTTTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774913 | GGATAATACATTTGC[-/TT/TTT/TTTTT]TTTTTTTTTTTTTTT | 10451 |
rs375094170 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107741810 | AGGCCCCAAATACCA[C/T]ATGACTTGCATATTT | 10451 |
rs375099956 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107584771 | TACAGAGTATAAACA[C/T]ATAAAGCCATTAACA | 10451 |
rs375109866 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621949 | TCTTATGAAAATACA[C/T]TCTTTGGAAAGCACA | 10451 |
rs375123498 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107739302 | CTTTCGCATGTTTCC[A/G]GATCAAACAGGCTAT | 10451 |
rs375147159 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107652796 | TTATTTGTGCTTCTA[C/T]CCAACTATCAATATG | 10451 |
rs375150488 | snp | A/G | 3.50183e-05 | 0.00418425 | intron-variant | VAV3 | GRCh38.p7 | 1:107779500 | TCTATAACCTGAGAA[A/G]AGAGGAAAATACTAA | 10451 |
rs375169964 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107776599 | ATGGATGAAGTTCCA[C/T]AGCATTTGAATCTGT | 10451 |
rs375170736 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107823543 | AGCCTGTGGAACTCC[A/C]AATTTTAGAGATCAA | 10451 |
rs375171450 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107733607 | ATACACAAGCTTCGG[C/T]AGCCGATTCAATCAA | 10451 |
rs375181551 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809933 | AAGGTTTTAAGAATA[A/G]TTGAGCTACAGCATA | 10451 |
rs375196442 | in-del | -/ACA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107763384 | AAAGAAGGAAGAACA[-/ACA]CTCAAACAAGACTGA | 10451 |
rs375208261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107651509 | ATTATTTATTTATTT[A/T]TTTTCAAAAAGGAAG | 10451 |
rs375230120 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896596 | CACAAAACCTCCTGC[C/T]ACAATAAATCTAATC | 10451 |
rs375256978 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107861302 | TTTTGTAAAAGCCAA[C/T]GCTAATTAATATCAT | 10451 |
rs375259655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107890142 | TGCACTAAAATCACC[A/G]TATCAGCAAGAAGTA | 10451 |
rs375265086 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107737576 | TCTCAAAAGAAGACA[C/T]TTATGCAGCCAACAG | 10451 |
rs375285827 | snp | G/T | 0.000153988 | 0.00877328 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573282 | GTGCAGGCTTCTATT[G/T]ATCCCTTCTCTGAAA | 10451 |
rs375313506 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107916935 | AAAACTGTGTGACGC[A/G]CAAGACAAGTTGAGG | 10451 |
rs375349220 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107924392 | AGTCGATATTATGAC[-/A]AAAAAAAAAAAAAAC | 10451 |
rs375370524 | in-del | -/G | 0.0115144 | 0.0749975 | intron-variant | VAV3 | GRCh38.p7 | 1:107719764 | CACATGAACACATAT[-/G]TTTATTGTGGCACTA | 10451 |
rs375379736 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107804294 | TGTTGCTTGTTTTCT[G/T]GTTGCTTTGTAACTC | 10451 |
rs375383698 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107674508 | TCCCACTGCTAATTT[G/T]CACAGAACTATACAG | 10451 |
rs375387524 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107788854 | TCTGCCTTTAAGCAG[A/G]TAGTAGAGAGAATAA | 10451 |
rs375395688 | snp | C/T | 0.00065697 | 0.0181122 | intron-variant | VAV3 | GRCh38.p7 | 1:107749426 | TAATGTTCAAGATTA[C/T]AAGTAAATTACAGTT | 10451 |
rs375401250 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107768646 | CCAAAATTGTAGAAA[C/T]TATTTTCTCTAACTT | 10451 |
rs375404419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620376 | ACCATACTTTTACTG[C/T]ACTTTTTCTATGTTT | 10451 |
rs375421794 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723810 | CTCTGTTGTAAATTA[C/G]AACAAAAACAATAAC | 10451 |
rs375454460 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107835266 | TGCCATGGCCCCACA[G/T]GAGTGCTTTCCTGGA | 10451 |
rs375481859 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107932218 | CCCAAATCACAGCAC[A/G]AGAGATGCCACACAA | 10451 |
rs375498185 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107655923 | TACCCCATTTAGAAT[G/T]GCTTTTATCAAAAAG | 10451 |
rs375509538 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702808 | TTCAAAAAAAAAAAA[A/C]AAACCTGATTTTTCA | 10451 |
rs375521950 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107703660 | AATGAGCTATTCTCT[A/G]TTTCACTCTTTTTCA | 10451 |
rs375533342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720714 | TTAGTAACATTCTAG[A/G]CCCAGTGGGACTTAC | 10451 |
rs375541263 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107917600 | GAACACAAGAAAGAC[A/G]TTGAGTCTCAAACAT | 10451 |
rs375547901 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941349 | AATTTTTAGTCTTGG[C/G]CAACAGCATCTGTTG | 10451 |
rs375549173 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107604155 | AACTTAAAAGAAAAA[C/T]TCTGTTTAGATTGGT | 10451 |
rs375560810 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649079 | ACAAACAAAAAAAAA[-/A]GCAAGCACTGTATTG | 10451 |
rs375561630 | snp | A/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786273 | TTCTATACTTACTAT[A/T]TTTTGAATCTTCAAA | 10451 |
rs375575156 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619384 | TTGGGTGAACTGTTT[A/C/G]TTTCATTCAGCTGTG | 10451 |
rs375583475 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107599395 | ACTCTAAACAAAAGA[A/C]ATCGCTAAGCTTTCC | 10451 |
rs375586272 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107641823 | GGAAAAAATGCTCTG[A/G]TAAAGTAGGAATTTT | 10451 |
rs375594164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107674102 | TAGTTTTTCAGAACT[G/T]CATGATATTTAAAAA | 10451 |
rs375597450 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632310 | CTGGAAGTGAGGCTG[G/T]GTGTTGACATTATTG | 10451 |
rs375598639 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864615 | GCATGGAGGGTGAAA[A/C]CCTGTCTCAAAAAAT | 10451 |
rs375608836 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107704886 | ACCTATTGGCTAGAA[A/G]GTTAGAAAAGTCTGA | 10451 |
rs375612535 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650285 | GAAATTTATTGAACA[C/G]GTCAAGTTCTCATTA | 10451 |
rs375624258 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107875091 | TCTGTAACACTCAAG[A/C]CTGCTCTAAAAATGA | 10451 |
rs375656577 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772601 | CTCCAAATGCAGTAA[C/G]AAGTCATAATTATAT | 10451 |
rs375658665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107660601 | ACTGTGGCTGCAAAG[C/T]GAAGGAGATCCTAGG | 10451 |
rs375667378 | in-del | -/GTATATGTATAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107728600 | TATGTATACGTATAC[-/GTATATGTATAT]GTATATGTATATGTA | 10451 |
rs375695892 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809535 | TTATAATGTGCAAAA[A/C]CCTGTCATAAATATT | 10451 |
rs375711579 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107722245 | TTGGGTTTTCTTCCC[A/C]ACTCAAAACTAATTA | 10451 |
rs375718176 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107715256 | AAGACAAGTGAGAAC[A/G]TATATGTGTGCATTT | 10451 |
rs375722768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746670 | TTGCCAGCCTCCCTC[A/G]GCAGGTGCGGCCACA | 10451 |
rs375723402 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107727872 | CCCAAGACAAACTCA[A/G]TCTAAGGGGAGTTTC | 10451 |
rs375755371 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107724234 | AACAGTTATTCCTAG[A/T]CATGAATAGTCTTCC | 10451 |
rs375764116 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107900599 | CATGTTGATAAGTGC[A/C]GTCCATTTACAGAGG | 10451 |
rs375770168 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107600370 | TCTTTTCATAATTAC[A/T]TCCTTTGCTAATGTT | 10451 |
rs375774714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107821827 | GTTTCCTCACTCTCC[A/G]CTTGCAGAGTCCAAT | 10451 |
rs375786491 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107759423 | AATCTGTGGTTTCAA[A/G]TCATCAAGCATTTCA | 10451 |
rs375822466 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107695581 | ATTTTAGTCATGAGA[C/T]ATTTGAGGTCAATGC | 10451 |
rs375828576 | in-del | -/TTC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726556 | CATCAAAAAGCCTTC[-/TTC]ACTAAAAGCTAGCAG | 10451 |
rs375860495 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908989 | ATATTAATTATTCCA[C/T]TAAATTATATACTTT | 10451 |
rs375869134 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864163 | TACAAAATGCAATGT[A/T]TACATATTACATCTA | 10451 |
rs375894528 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107839066 | AATATACCTCTGTAA[C/G]AAACCTGCACATGTA | 10451 |
rs375900560 | snp | C/T | | | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688902 | CTTTTATTTTTAATT[C/T]TGGCAGAAATACAGT | 10451 |
rs375922081 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107879153 | TTGCTTTCTTATATC[A/C]AGTTGTCCCAGGTCC | 10451 |
rs375932837 | snp | A/G | 3.30437e-05 | 0.00406457 | missense, intron-variant | VAV3 | GRCh38.p7 | 1:107683530 | GCAGTCCATTGGTCC[A/G]TTTCTGTGCAGTAAA | 10451 |
rs375937748 | snp | A/C | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107768485 | CTGCTGCTGTCAGAA[A/C]TCTTTTTAGTGGTGC | 10451 |
rs375946462 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107711687 | CTGAGAGAAATAAAT[A/G]CATTCAATAAATTCG | 10451 |
rs375954726 | snp | C/T | 2.97075e-05 | 0.00385394 | utr-variant-5-prime, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964889 | GACGGCTCCGGGACG[C/T]GGCTGGGCCGGGGCG | 10451 |
rs375956631 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107807854 | AGCAATATGTTTCAG[C/T]GTACAAGTCCAGGAC | 10451 |
rs375957410 | snp | A/G | 8.27863e-05 | 0.00643322 | intron-variant | VAV3 | GRCh38.p7 | 1:107642794 | TAGAATTGAGAAAAC[A/G]ATGATGCATGAAGTC | 10451 |
rs375968889 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107888796 | AAATTATTCTCATAT[A/G]TATCAGTCACTGTTT | 10451 |
rs375971414 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847787 | TAATTAATAGCTGAC[C/T]AACTAAAAAAAGCCC | 10451 |
rs375979870 | in-del | -/TCTATA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107810466 | CATACTCTATTTATA[-/TCTATA]ACTAAAGAAATTATG | 10451 |
rs375998642 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107768860 | TAATATCTCCCAAAT[A/G]TTTTGTGGAGATTCT | 10451 |
rs376009981 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107741182 | TAACAAAGTGAATCT[C/T]TTAAATTTTCACATT | 10451 |
rs376021763 | snp | C/T | 1.68564e-05 | 0.00290309 | intron-variant | VAV3 | GRCh38.p7 | 1:107757344 | CCTATTTGGAAGATA[C/T]GGTTTAGTACTACTT | 10451 |
rs376023462 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107906935 | TCTTAGGCTTTCTTA[A/G]TTTAAAGCACATTTA | 10451 |
rs376026408 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814549 | CTTGTAGAATGAATA[C/T]ATATTTTGCAAATAT | 10451 |
rs376030332 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107805495 | TTCTCAGTTCCAAAT[G/T]TGTTTGATCTTTTAA | 10451 |
rs376035220 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107922877 | GAATGGCGTGAACCC[A/G]GGAGGCGGAGCTTGC | 10451 |
rs376042620 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753527 | ACATATATATATATA[C/T]GTATATATATATATA | 10451 |
rs376067332 | snp | A/G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107718446 | AAATCATGAGTGAAC[A/G/T]CCCATTCACAATTGC | 10451 |
rs376085128 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774642 | TACGGGCATGTCTGG[C/T]GCCCTGATACTAAAA | 10451 |
rs376092564 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107703562 | GGTCCTTTTAAAATG[A/T]CTGAGAGGAATGTGC | 10451 |
rs376101191 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681875 | CCGTGTTAGCCAGGA[A/T]GGTCTCCATCTCCTG | 10451 |
rs376103235 | in-del | -/AG | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571597 | ACATTCCCGAGACAG[-/AG]TCGCAGATAAGACTT | 10451 |
rs376103337 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107880836 | AGCACCAAAGGAAAG[C/T]GGAATACTCAGCTTT | 10451 |
rs376105840 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107731528 | CTATTTGGGCCCAAG[A/T]AGTGATATTAGGAAA | 10451 |
rs376110488 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774929 | TTTTTTTTTTTTTTT[A/T]AGATAACCCTACTTC | 10451 |
rs376112190 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701686 | CACTTCTCTTTTAAA[C/T]ATAAGTTCCAATTTC | 10451 |
rs376116808 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833265 | ACAGTGAAAGTTTTC[A/G]TGGTCTGGATAGATC | 10451 |
rs376125469 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790151 | CCATGGCCTCTTCAG[C/T]GGAACCAGAAGAAAG | 10451 |
rs376129595 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107816133 | GCCATGGACCTGGTA[C/T]TTGTCTGTGGCCCAG | 10451 |
rs376146727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914540 | AGTGAGCTAATGCCC[A/G]TGAAAGCAATCCGTA | 10451 |
rs376154230 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107886094 | TGGCCAAAATTTTGG[A/G]GGAAATGCAGGAATT | 10451 |
rs376156399 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107853585 | CAAGAACCAAAAAAA[-/T]AAAAATTCATTTATA | 10451 |
rs376159792 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107834694 | TAAACCAACATACTT[C/T]GAACAGATCTTTGGA | 10451 |
rs376171787 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941006 | AATTGAAAAAAAAAA[A/C]CCCTCAACTAGAAGA | 10451 |
rs376184027 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871922 | AGTAAACAACTTTAA[-/C]CCACCACTGGGCTGC | 10451 |
rs376187292 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107924660 | ACCAAACTGATTTAA[A/C]TGACAGTAGCTAAAA | 10451 |
rs376208706 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107940899 | GGATGGTGGTGATGA[C/T]TGCACAACAGTGTGA | 10451 |
rs376222631 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107576620 | CATTTTGATAGACAA[C/T]AGTATTTTGCAATTC | 10451 |
rs376224944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107798635 | GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC | 10451 |
rs376230382 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107701846 | GGACCACCTCAGCCC[A/G/T]AACTTCATTGTCCAC | 10451 |
rs376248965 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673248 | GCTGCCCATGTCACT[A/C]CTCTGGATAAAACCT | 10451 |
rs376260001 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107620760 | GAGAAAAGAGGATGA[C/G]AACCCAAAGAATAAA | 10451 |
rs376266360 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107600789 | ACTGCCTTGAGCTGA[A/G]CCCAGGTGACACAAA | 10451 |
rs376308394 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107884663 | CTATGTTTCCCAGTC[C/T]GGTCTTGAACTCCTA | 10451 |
rs376316953 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, upstream-variant-2KB, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107755445 | ATTCTCTATAGATAG[C/T]TGAAACTGTTTAATT | 10451 |
rs376317574 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107773982 | CTGCAAAAAAGTCAA[A/C]CTTGCTGAAGTCCTA | 10451 |
rs376332911 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925786 | AACAATGTGGACACA[C/T]ACTTAATGCTATTGA | 10451 |
rs376346063 | snp | A/C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107597991 | AAGTCACATAGCTAG[A/C/T]GCCTTTATCCAAAGT | 10451 |
rs376355345 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107867371 | GGGTACTAAAGTTCT[A/G]TAAGAGGAGGTAGGA | 10451 |
rs376358720 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107961411 | TACAGCTATCACCAG[C/T]AGGCTCTTCTCTTCC | 10451 |
rs376364456 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107828635 | TATGGACACATAGCC[C/G]TCTTCCTCCATCTTC | 10451 |
rs376374732 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107800560 | ATTTTAGATTCAGGA[C/G]GTATATGTGCAGATT | 10451 |
rs376376598 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107945231 | ATTAACATGAAAGAT[C/T]ATATAAGAAAAAAAC | 10451 |
rs376388106 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107931176 | TAAGAAATCTGAATA[C/T]GGACTGTATGTTAGA | 10451 |
rs376408591 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107754059 | GCAGAACTGTAGAAA[C/T]GTATGTCAAATTGGA | 10451 |
rs376418840 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107737995 | ATTAAGAGAATGTGG[C/T]ACATATTCACCATGG | 10451 |
rs376429112 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898080 | TTTATTACTCCTTTG[A/G]GCAAAGAATGTCATT | 10451 |
rs376430056 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107752510 | AATATCAACAGAGTG[-/A]AAAAGCCAACAGACA | 10451 |
rs376431021 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717901 | GGTATCTAAGGACTT[C/G]CTTTATGAATCTGGG | 10451 |
rs376448032 | snp | A/C | 2.0405e-05 | 0.00319407 | intron-variant | VAV3 | GRCh38.p7 | 1:107760902 | AATGTTTTAAAAACA[A/C]TTTGTTAGGGAGTCA | 10451 |
rs376454093 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107778095 | TTTCAGGCAGCCAGC[A/C]TATCACATGTTTCAT | 10451 |
rs376457338 | snp | C/T | 0.000277218 | 0.01177 | intron-variant | VAV3 | GRCh38.p7 | 1:107779539 | GTAGTTCAGAAAATA[C/T]AAGATTTCTTTTTCC | 10451 |
rs376458921 | snp | C/G/T | 0.000230615 | 0.0107358 | intron-variant | VAV3 | GRCh38.p7 | 1:107749444 | GTAAATTACAGTTAT[C/G/T]AGTTTCCAAAAAGTC | 10451 |
rs376473172 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107904300 | TAAATGTATACGTAT[G/T]ATGTGACTGAATGAT | 10451 |
rs376478984 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107599844 | CAATAACAAGAGGAT[A/C]CTGAACTATTCTTAA | 10451 |
rs376482142 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920787 | TGTACCTCTTACAGT[C/G]ATCAGCACATTTTCC | 10451 |
rs376510473 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950084 | GAGCTTCTGGTTCAT[C/T]GATAACGCTCTCCAA | 10451 |
rs376511937 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107648482 | TTTTATTGGAAAAAA[C/T]GTTTCCCTAAAATAT | 10451 |
rs376513227 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107883909 | CATACAAAAGGAAGA[C/G]AAGCAGCATCTTTAC | 10451 |
rs376516153 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962683 | CAGGCTCAGGTACTA[A/G]CCTTCTAGGATTCAC | 10451 |
rs376529316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760681 | TCAAAATTTTAAGGG[A/G]ATTGGGCCCAACACA | 10451 |
rs376541574 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107658940 | TTTTGCTGTGCAGAA[C/G]CTCTTTAGTTTAATT | 10451 |
rs376551056 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107953283 | TCATAGACATGAGGA[C/T]TGGGGAGGCAGTGGG | 10451 |
rs376559555 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107623076 | ACAGCTGCAGCCATA[C/T]TGTAACCATCATCAG | 10451 |
rs376560158 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107932205 | CTAACAAAAGGTACC[A/C]AAATCACAGCACGAG | 10451 |
rs376566435 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107676852 | CAGATCATTCATAAC[C/T]TATACGACACACTTT | 10451 |
rs376566658 | snp | A/G | 3.30868e-05 | 0.00406723 | intron-variant | VAV3 | GRCh38.p7 | 1:107596350 | CAAGTTCCTTTGGAA[A/G]AAAGAATCCAACATA | 10451 |
rs376575240 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107713371 | TTTATTTAAATAAAA[A/G]AAACACATAAAAAAT | 10451 |
rs376575863 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753528 | CATATATATATATAC[A/G]TATATATATATATAT | 10451 |
rs376581564 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814972 | AGAACTTGGTGACAA[C/T]TGATTCCAGAAAATG | 10451 |
rs376599670 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107676612 | AAAACTTTTTTTTTT[-/T]CCTAAGCTAGTTTGA | 10451 |
rs376619506 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107619808 | TCTATAGAATGCAGT[A/G]TACAGGAGAATAAGT | 10451 |
rs376620046 | in-del | -/GTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774079 | TTTGCTGTTGTTGTT[-/GTT]TGGGGGACAGAGTCT | 10451 |
rs376631438 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107730319 | AAACACACATATTTA[C/T]TTAACGATCATCTGA | 10451 |
rs376634691 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107767704 | TTATCAGTGTATGTG[C/T]ACATGCGTGCATGGG | 10451 |
rs376641143 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928054 | CACCCCCAGCTCCAG[-/G]TGGCTCAGAACAGAA | 10451 |
rs376641363 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650950 | CACCATGGAATACTA[-/T]GCAGCCATAAAAATG | 10451 |
rs376660170 | snp | C/T | 1.65075e-05 | 0.00287289 | splice-donor-variant | VAV3 | GRCh38.p7 | 1:107772734 | CAAGTAAAAGTCCTA[C/T]GGGCTGATGTGCTTC | 10451 |
rs376666687 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658052 | AATTTACCTACTGGG[A/C]ACAATACTTCAATAT | 10451 |
rs376679089 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736865 | ACTACTTTAAAGTTC[A/T]TATGGAAACAAAAAA | 10451 |
rs376708924 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | VAV3 | GRCh38.p7 | 1:107922844 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCGG | 10451 |
rs376710253 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107707749 | ATCTCTTCAGTTCAC[A/C]CTGAAGTACAAACTG | 10451 |
rs376719576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107948228 | CCCTAAACTACTGCA[C/T]CCAAAAAATGAAAAA | 10451 |
rs376720993 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107705354 | GGTCAACCTGCCTGG[-/A]AAAAAAAAAAAAAAA | 10451 |
rs376744064 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107872397 | CACCAATGTAGGAAA[G/T]GAGGCAGACAGGAGA | 10451 |
rs376747739 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107843102 | TTTGGCTGTTCCAAT[C/T]TATCGTGAAACCTAT | 10451 |
rs376754475 | in-del | -/AAAAA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107722855 | ACTTAGTAAGCGTAC[-/AAAAA]AAAAAAAAAAAAAAA | 10451 |
rs376760794 | in-del | -/AA | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107645174 | TGTGTAACCCTTGCC[-/AA]GAATTATGCTTAAGC | 10451 |
rs376782453 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571561 | CTCCATAACAAAGTT[C/T]GGCTGACGGCAACAG | 10451 |
rs376786032 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107816908 | TAAGCCTTTACTGAT[A/C]ATTGGTAGGCAAAAG | 10451 |
rs376789192 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107612763 | GAATTTGAGGTTTCC[C/T]CTCTCTGACTCTTTT | 10451 |
rs376798819 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107638722 | CAAGGAAACCCAAAA[C/T]ACCTATGAAAAAAGG | 10451 |
rs376801742 | snp | C/G | 2.1215e-05 | 0.00325685 | intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964643 | GCCGGCTGGAGGCGG[C/G]GCGCCCGTGCCGGCC | 10451 |
rs376802192 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107700050 | CACTACAATTAAATT[A/G]TAAGTGCAAGTGAGT | 10451 |
rs376807471 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756491 | GGTAGACAATCAGCC[A/G]AACAGCGAAGCTAAC | 10451 |
rs376830393 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107803015 | TACGGCTTCAATCTT[A/G]TTGCTCCTTATTGGT | 10451 |
rs376844764 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662575 | TTCATTAAAAGCACT[A/G]AGAGTTGAATGGATT | 10451 |
rs376856930 | in-del | -/ACC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107801074 | CTTATTAAAGAAACC[-/ACC]TTTTGCCCACTGTAT | 10451 |
rs376858844 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107585360 | TCATCTATTTTCATG[G/T]TTTTTTTTATTATAA | 10451 |
rs376872096 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107601554 | AGTGGTCCTTCCCAA[C/T]GTTACTCAAGGTACT | 10451 |
rs376891648 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107696329 | TGCTCTTCCAGCTAT[C/T]TGAAAATATACAATA | 10451 |
rs376920462 | in-del | -/ACTTTGA | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896275 | TAGAGACACAGACTT[-/ACTTTGA]GCAAGTCCTTAAGAA | 10451 |
rs376921887 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107748712 | GAACTAAAACATGCC[C/T]ATAAGAAAGTCAAAC | 10451 |
rs376924055 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107759263 | TTTCTGCTATAAACA[A/G]GAACTTAAAGACAGA | 10451 |
rs376928801 | in-del | -/AG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107711759 | CCCAGGCTGGAGTGC[-/AG]TGGTGCAACCTCTGC | 10451 |
rs376941305 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107771402 | TGACTACAGGTGCCC[A/G]CCGCCACGCCCAGCT | 10451 |
rs376941571 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107634458 | CTTCCTTACACCTTA[C/T]ACAAAAATTAATTCA | 10451 |
rs376942699 | in-del | -/G | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107843791 | GTCTTTTGCCTGTTC[-/G]AGTTGTGACAGATAA | 10451 |
rs376951404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864662 | AATGTGTGAGTACTA[A/G]CATCCCCTTCTCACT | 10451 |
rs376968025 | in-del | -/TTTA | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107856610 | ACTAATTGATAGCAC[-/TTTA]TTTTGTTCTCAAGTT | 10451 |
rs376972130 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107670517 | TGTTATTGAAAAAAA[-/A]CTGGCAAGAGACATG | 10451 |
rs376983907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690871 | GGCCTGCTGCATTCA[C/T]GGATACGGCATAGAG | 10451 |
rs376990607 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107841297 | GGGGAAAGGGGGGGG[-/G]TAGAAAAAGAAACAA | 10451 |
rs376996016 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107888727 | GCCTCCCAAAGTGCT[A/G]GGATTACAGATATGA | 10451 |
rs377000322 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857743 | TATCGACTGACTGTG[C/G]CTGATTCCTGTCTCA | 10451 |
rs377010035 | snp | C/T | 0.000116693 | 0.00763759 | utr-variant-5-prime, intron-variant | VAV3 | GRCh38.p7 | 1:107688480 | CCTTAGCTTTCTCTG[C/T]AGAGTGGTAAAACAC | 10451 |
rs377036828 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107599545 | GACATGGACTGTCTC[A/G]CATACATGAAAATTA | 10451 |
rs377047650 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107682010 | TCTCTTGTAAGTTTA[A/T]TCTTCATGAAGTTCT | 10451 |
rs377049809 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107879247 | TTTATACAATAAATA[C/G]TATTTGGAAACCACC | 10451 |
rs377050618 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107598718 | TTTGCGCAGACAAGG[C/T]ATAGAATTAAATTCT | 10451 |
rs377054790 | in-del | -/AA | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107611458 | AATAAACTGATCTTC[-/AA]TAGTTCACCCTTTGA | 10451 |
rs377057379 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107768594 | AACAAACAACAAATA[C/T]GTTTTGAAAGTCAAT | 10451 |
rs377076125 | snp | A/G | 9.9486e-05 | 0.00705217 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107757276 | CTTCATGGCATCAAG[A/G]GCCAGTTTCAGATTT | 10451 |
rs377080778 | snp | C/T | 3.62207e-05 | 0.00425547 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107749046 | AACCCATTTTGTCCT[C/T]GGGTATGGATGAGGT | 10451 |
rs377089465 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107864033 | TGAAGTATACCCAGG[C/T]TTAAAAGCCTCTGCA | 10451 |
rs377107328 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107842292 | AGGGAAGGGAGTTGC[A/G]AGATGAATAGCTAAA | 10451 |
rs377111953 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107615879 | AATCATTAAAGAAAT[A/G]CAAATTGAAACCACA | 10451 |
rs377112758 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107648198 | AAATAATGGAAATAG[C/T]ACTGTCACAGCTCAT | 10451 |
rs377124734 | in-del | -/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107912060 | TTTTGTTTGTTTGTT[-/TG]TGTGTGTGTGTGCGT | 10451 |
rs377135527 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856988 | AGGTTACAGTGAGTT[A/G]GGATTGCACCATTTC | 10451 |
rs377138310 | snp | C/T | 9.90966e-05 | 0.00703836 | missense, utr-variant-5-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107751153 | TCTAGAGTGGTTATT[C/T]GAATTTCACCATCTC | 10451 |
rs377139276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107870768 | TGAACCTGAACATGA[C/T]GAAACTATCCTATTG | 10451 |
rs377145033 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720925 | GTCAGAGAAGATAAG[G/T]TATGAGAGGATAATT | 10451 |
rs377150180 | in-del | -/T | | | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690480 | AGAAGAGAGGATCCA[-/T]CATAGAACACCAGAG | 10451 |
rs377153428 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107765889 | TAGTACTAGGAAATA[C/T]GTTGCTTGATTTGAA | 10451 |
rs377154290 | in-del | -/AT/ATAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107843365 | CTTAGCACAACACAA[-/AT/ATAT]ATATATATATATATA | 10451 |
rs377166936 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107650654 | ATGCTGGTGTGCTGC[A/T]CCCATTAACTCATCA | 10451 |
rs377185091 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892576 | TAACCAACATTTCAT[C/G]TTTGCTACCTGAATT | 10451 |
rs377197893 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107619771 | TTCCACTCTTCTTCA[A/G]AACAACAACAAAAGG | 10451 |
rs377205195 | snp | A/G | 0.000252626 | 0.0112361 | intron-variant, stop-gained | VAV3 | GRCh38.p7 | 1:107785493 | GGCAATCAGGCAGCT[A/G]CATGCTAGAGCCCCA | 10451 |
rs377223261 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790679 | TCCTTAAATGTCTTC[C/T]TTTTTTTTTTTTTTT | 10451 |
rs377244284 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902236 | GTCTCTACAGACTTT[A/G]CCTAGTTTTCTGTGC | 10451 |
rs377278848 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107934669 | CACATCAAAAGTCTC[A/G]AAAAGGAAACTCTTA | 10451 |
rs377310582 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107699793 | CAATTGCAAAGGAGA[A/C]AGAAATCCAGGTTCA | 10451 |
rs377317531 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947471 | CAGGAGAAGGGAAAG[A/G]ATCTCACATGATTAC | 10451 |
rs377325463 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959812 | GATGTCTACTAGGCA[A/C]TTCAATCATAACTAG | 10451 |
rs377358282 | snp | A/C | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593200 | AATTCTAATCAATAT[A/C]TTTTTAGATGTTACT | 10451 |
rs377367526 | snp | C/T | 1.65636e-05 | 0.00287776 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874939 | ACAAGTCAAATGCCT[C/T]GAAAAGTTCACTTTT | 10451 |
rs377368882 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628107 | GTATTGTGCCTTGAT[C/G]ATAAGGAAGGATTTA | 10451 |
rs377398470 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107603133 | AATAAGTTCGGTCTC[C/T]GCTTGCAATCTTTCC | 10451 |
rs377399700 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107718888 | AACAGAACAGAGGCC[A/T]CAGAAATAACACCAC | 10451 |
rs377405878 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908107 | AAGCTCTTTCACAGT[A/G]CCTGGAAGCCTGGAA | 10451 |
rs377407894 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107852552 | CATTAATTGTGAGGA[C/T]TTATTTCATTCCATT | 10451 |
rs377422505 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107795733 | GTTAGGGCTTTAATA[C/G]TTTAGAAACAGAAAT | 10451 |
rs377423802 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107587249 | ACCCTAGCCGAATAT[A/G]TAGTCAGCTTATTAA | 10451 |
rs377425556 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107837563 | ATATGGAACCAAAAA[-/A]GAGCCCAAATAGCCA | 10451 |
rs377437322 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892190 | CAATCATTTAACCCA[C/T]GAGAGTCTTGGTTTG | 10451 |
rs377438864 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856142 | TGAGAGAAAAGCCTA[C/T]GGTCAGCAGCAGGAC | 10451 |
rs377452810 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840010 | TCAGCTAAAGAAGTC[C/G]AATTAATAATTAATA | 10451 |
rs377455591 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107810438 | TCCCTTTCCAGTCAT[A/T]CTTTCAATTCCACAT | 10451 |
rs377458052 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107850023 | CAAAACCATGAGATA[C/T]CATCTCATGCCAGTT | 10451 |
rs377463908 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898531 | CTGTTACTTAATACA[C/T]CCATTTACATTATTA | 10451 |
rs377469296 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107735270 | GGAAAGATCTAAAAT[C/T]GACACCCTAACATCA | 10451 |
rs377477300 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701342 | CCCTCTGAAGCAACA[-/G]GCCTGAGCTGTACGT | 10451 |
rs377485022 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788327 | AGAAGTCCCCAGGAG[C/T]TGCTGCCCTGCCCCT | 10451 |
rs377490158 | snp | A/C | 1.73763e-05 | 0.00294752 | intron-variant | VAV3 | GRCh38.p7 | 1:107751094 | AATTACTTATTTTGA[A/C]AATAGTATTCTTCTT | 10451 |
rs377492893 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107802675 | GTTGAACTATCATAT[A/C]CTAGGATGCATCCCA | 10451 |
rs377495673 | snp | A/G | | | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587738 | TGGGATTACAGATGC[A/G]TGCCACCACACCGGG | 10451 |
rs377495764 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959556 | CCAAAAATACTCTGT[C/T]CACTTGGTTTCCCTC | 10451 |
rs377496226 | in-del | -/AT | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107629046 | TTATTTTTGGCACTG[-/AT]TACAGTTCTACTGCT | 10451 |
rs377498341 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107643982 | CTACATCCTCCTTTG[C/T]TTCTGTTCTTGTGCC | 10451 |
rs377505379 | snp | A/C | 1.6656e-05 | 0.00288578 | intron-variant | VAV3 | GRCh38.p7 | 1:107573421 | ACTTTGTATCTGACA[A/C]TTCAAAGGATTCTAC | 10451 |
rs377515085 | snp | C/T | 1.65389e-05 | 0.00287562 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874977 | CCAAACGTCTCACAA[C/T]AGGCCGTGAGAAATG | 10451 |
rs377550224 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107665310 | AAGGGGTGCATTGTC[C/T]GGGGATAATTTAAAA | 10451 |
rs377551873 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673613 | CCAGGACATAGGGAG[C/T]TGTGTGAGGGAAAAC | 10451 |
rs377580041 | in-del | -/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107624375 | TTATAGTCTTATGAC[-/TG]TGTGTGTGTGTGTGT | 10451 |
rs377590938 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107659979 | CTTCCCTTTCCCCCA[C/T]CTCAAGACACAGGAA | 10451 |
rs377593193 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959521 | CTTGATCAGCAGCAT[C/T]TGACATGTCATCGCT | 10451 |
rs377617523 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107674250 | GAGTGAGTTCTGCTG[G/T]GTGTCATACACATGG | 10451 |
rs377617538 | snp | C/G | 0.0021876 | 0.0330002 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573273 | CACGATGCTGTGCAG[C/G]CTTCTATTTATCCCT | 10451 |
rs377623435 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107705166 | ATCAGGTAGAGATCT[G/T]ATTCAAGCAAAATGA | 10451 |
rs377649647 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769333 | CTAAGAAGTTAAGCA[C/T]GGACATTACCGATCG | 10451 |
rs377652125 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107696729 | ACTCCCTTGCTTTCA[A/G]TTTGGCTGTTGAAAT | 10451 |
rs377661801 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107749212 | ATCAAGCTTATTGTA[A/G]TCAACTTCATATCTA | 10451 |
rs377662673 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107797987 | ACCACTGACATAGAG[A/C/T]GATAAGCCATGAAGA | 10451 |
rs377674551 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107763299 | TCCCTAAGTCGAGCA[C/T]TGACTGCAAAAACTA | 10451 |
rs377708717 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790876 | TATTTTTACTAGAGA[C/T]GGGGTTTCACCATGT | 10451 |
rs377736931 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107781822 | TATTGATTAATTCCC[C/T]ATAATAAAGATAAAA | 10451 |
rs377745482 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107873846 | ACCATGGGTTAAGAC[C/T]GGAGAGAGAACCAGG | 10451 |
rs377746457 | in-del | -/AGAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681345 | ACTGATCCCTTGTTT[-/AGAC]AAACATTTTGTCTGA | 10451 |
rs377751417 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107579436 | GTCCCATGTTTCCCC[C/G]CTGCAAGAACTCTCC | 10451 |
rs386354219 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107880821 | AAGAAAAGAAAAAAA[-/A]GCACCAAAGGAAAGC | 10451 |
rs386367985 | in-del | -/TAAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720392 | GTCTCAAAAATAAAT[-/TAAA]AAATAAATAAATAAA | 10451 |
rs386367987 | in-del | -/TT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774914 | GATAATACATTTGCT[-/TT]TTTTTTTTTTTTTTA | 10451 |
rs386367988 | in-del | -/TT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774927 | CTTTTTTTTTTTTTT[-/TT]TAAGATAACCCTACT | 10451 |
rs386367989 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107880815 | AAAAAAAAGAAAAGA[-/A]AAAAAAGCACCAAAG | 10451 |
rs386367990 | in-del | -/AA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933815 | ATGAGACCCTTCTCA[-/AA]AAAAAAAAAAAAAAA | 10451 |
rs386634378 | in-del | CCCAGTG/TT | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595420 | AATACCTCTAGATAT[CCCAGTG/TT]TTGCTTAGGCTAAAG | 10451 |
rs386634379 | multinucleotide-polymorphism | AA/CG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107600481 | GCCCAGATATGGAGA[AA/CG]AAAACACATATGCAC | 10451 |
rs386634380 | multinucleotide-polymorphism | CT/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621248 | TGGTCATAGGCATTC[CT/TG]TAGATGACAGAGAGG | 10451 |
rs386634381 | multinucleotide-polymorphism | GGCCAGCTATTC/TGCCAGCTATTT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107670227 | TCACTGCTGGCTCTT[GGCCAGCTATTC/TGCCAGCTATTT]CGTGCCAAGCAAGCA | 10451 |
rs386634382 | multinucleotide-polymorphism | CA/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681949 | ACAGGCGTGAGCCAC[CA/TG]CACCCAGCCACGTAT | 10451 |
rs386634383 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693984 | GAACCCATGTGTCAA[-/T]TGGCAAAGTCACAAG | 10451 |
rs386634384 | multinucleotide-polymorphism | ATAAATTTTAAGCATTTTTCTAATTGTGCTTATAAG/GTAAATTTTAAGCATTTTTCTAATTGTGCTTATAAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107704391 | ATGCAGAAAACTCAC[lengthTooLong]TAATAGTTTCAAAAG | 10451 |
rs386634385 | multinucleotide-polymorphism | AG/GC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723324 | TGCTTATGCTGTGTT[AG/GC]TGCCCTTCTGTGTTT | 10451 |
rs386634386 | multinucleotide-polymorphism | CC/GG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107734550 | CAAAAGAAAAGCAGG[CC/GG]TTGCAATCCTAGTCT | 10451 |
rs386634387 | multinucleotide-polymorphism | CA/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107746032 | TTTTCTTTTATTCTC[CA/TG]TGACTTATCAAAAAG | 10451 |
rs386634388 | in-del | CTACTGG/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107772910 | ATAGCTACAAATAGC[CTACTGG/T]ATTTTAGTAAAAAAT | 10451 |
rs386634389 | in-del | -/CTC/TT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107794352 | TTGATTCATCATTTT[-/CTC/TT]CCTTCATCTTGCTTT | 10451 |
rs386634391 | multinucleotide-polymorphism | AT/GC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107811839 | GCTCCTCCGAAAACT[AT/GC]CTTTGGACTTCTAGT | 10451 |
rs386634392 | multinucleotide-polymorphism | CG/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107817167 | GACGCATTATGATAG[CG/TA]GGCAGACAAAAAATT | 10451 |
rs386634393 | multinucleotide-polymorphism | AA/GC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107855612 | TTAAATTTGTTAAGA[AA/GC]AGGGGCAGGAATTGT | 10451 |
rs386634394 | multinucleotide-polymorphism | CA/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107873798 | AGGCAGCCTGATGCC[CA/TG]AGAAGGCTGGTGCCT | 10451 |
rs386634395 | multinucleotide-polymorphism | AT/GA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107904219 | CTTCCTTCCTCAATT[AT/GA]GTTAAAATGCTGATT | 10451 |
rs386634396 | in-del | G/TCT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907689 | CACACACACACGCGC[G/TCT]CTCTCTCTCTCTCAT | 10451 |
rs386634397 | in-del | A/TTTGT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107949313 | TTTTGTTTATTTTTG[A/TTTGT]TTGTTTGTTTTGAGA | 10451 |
rs386634398 | multinucleotide-polymorphism | AA/GT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952723 | TATGAAGTAAAACCC[AA/GT]ACTGTATAGACTAAA | 10451 |
rs386634399 | multinucleotide-polymorphism | ATATTTCTCC/GTATTTCTCA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107958749 | CGTCATCTACGTTAG[ATATTTCTCC/GTATTTCTCA]TAATGTTATCCCTCC | 10451 |
rs397694124 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107892626 | AGTTACAAAAAAAAA[-/A]TGATGTGGACTCCTC | 10451 |
rs397705511 | in-del | -/AAA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107609561 | AAATAAAAAAAAAAA[-/AAA]CTACTACTGTCCTTT | 10451 |
rs397764471 | in-del | -/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947400 | AGTTCTAAGAGTTCC[-/C]AAAAGAACTGTGAGG | 10451 |
rs397789569 | in-del | -/A | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107948332 | TTGTAAAAAAAAAAA[-/A]TTGTAAGAGAATAAA | 10451 |
rs397797395 | in-del | -/GA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107922297 | TTTTTTCTGGATACT[-/GA]GACACAAAACAAGAC | 10451 |
rs397836183 | in-del | -/AC/TA | 0.0134798 | 0.0809826 | intron-variant | VAV3 | GRCh38.p7 | 1:107612143 | Ttatatatatatata[-/AC/TA]cacacacacacatac | 10451 |
rs397843999 | in-del | -/CAAA | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966519 | AAACAAACAAACAAA[-/CAAA]CAAAAAGATGGGAGT | 10451 |
rs397861439 | in-del | -/T | 0.468148 | 0.122112 | intron-variant | VAV3 | GRCh38.p7 | 1:107771254 | AGTTTTCTTGTCAGC[-/T]TTTTTTTTTTTTTTT | 10451 |
rs397935875 | in-del | -/TCCC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107664347 | GATGCTCTCCCTCCC[-/TCCC]CAACCCCCCACAAAA | 10451 |
rs397942435 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107876954 | TTGGTTTGTTTTTTT[-/T]AATTTGCAGAAAGCA | 10451 |
rs397954956 | in-del | -/TA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107804863 | GTGGTGAATTCTCTA[-/TA]AACTTTTGTCTGTCT | 10451 |
rs397957765 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107955327 | CTATGTTTTTTTTTT[-/T]AATTTGTAGATGTTT | 10451 |
rs397958533 | in-del | -/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107601621 | TCTTCATTATCTCAG[-/G]AAACTACCAAACTTG | 10451 |
rs397978554 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107757050 | GTAAAAAAAAAAAAA[-/A]TCCAGTTTTCTCCAC | 10451 |
rs397981128 | in-del | -/A | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107625270 | TGCCGTCCCAAAAAG[-/A]AAAAAAAAAAAAAAA | 10451 |
rs397981129 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107761409 | TCTTTTTCTTTTTTC[-/T]TTTTTTTTTTTTTTT | 10451 |
rs397981130 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107766920 | TAGTGAGATAATTTC[-/T]TTTTTTCACAGGATG | 10451 |
rs397981131 | in-del | -/TAGA | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107769317 | CCATGCTTAACTTCT[-/TAGA]TAGAGTCACAAAATA | 10451 |
rs397981132 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107775604 | GCCGTGATGCTATTC[-/T]TTTTTTTTTTTTTTT | 10451 |
rs397981133 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107813133 | TAATTTTATCAAGAG[-/T]TTTTTTTTTTTTTTG | 10451 |
rs397981134 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107879722 | AGCAAAGTTGTACAA[-/T]TTTTTTTTTTGTCAA | 10451 |
rs397981135 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107922978 | CATCAAATTGTGCTC[-/T]TTTTTTTTTTTTTCT | 10451 |
rs397981136 | in-del | -/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107926583 | CTACTACCAGGAGAT[-/G]GGGGGAGGGGTGGCA | 10451 |
rs397981137 | in-del | -/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107941006 | TCTTCTAGTTGAGGG[-/T]TTTTTTTTTTCAATT | 10451 |
rs398049563 | in-del | -/T | 0.5 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107746896 | TCTTTTTTTTTTTTT[-/T]CAAGACGGAGTCTCA | 10451 |
rs398053330 | in-del | -/CAC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107609117 | AACAACAGTCACCAC[-/CAC]TTTTCTTATATAAAT | 10451 |
rs398074250 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892625 | TAGTTACAAAAAAAA[-/A]ATGATGTGGACTCCT | 10451 |
rs398074251 | in-del | -/A | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896747 | AATCTGTATTAAAAA[-/A]ATGGCTACAGGAATG | 10451 |
rs398074252 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107948331 | ATTGTAAAAAAAAAA[-/A]ATTGTAAGAGAATAA | 10451 |
rs398089504 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809611 | GAAAGGACCAGAAAA[-/A]TATATTCAAAATGCA | 10451 |
rs398089505 | in-del | -/GA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107811908 | TAATATGGCCTGAGA[-/GA]TTTTGGTTTTAAGGT | 10451 |
rs398089507 | in-del | -/TG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107900792 | ACTTTGTGGTCTCTG[-/TG]AACTTAACAGACATA | 10451 |
rs398103154 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701071 | TTGAGCTTTTTTTTT[-/T]CATATATGTGTTAGC | 10451 |
rs398103155 | in-del | -/TC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701464 | AAAACCATTTCTCTC[-/TC]CTAGGACTCTAGGAC | 10451 |
rs527236745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699307 | AGGCCCCATGCAAGT[C/G]TGAAATCCAGCAGGG | 10451 |
rs527247095 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107761311 | GGCAGGAGAATGGAG[C/T]GAACCCGGGAGGCGG | 10451 |
rs527247733 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107782174 | GCAATAGCAGTACTA[C/T]GGTTATGTCTTTTAT | 10451 |
rs527260667 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107598701 | GGTGAATTTTAACAT[A/G]TTTTGCGCAGACAAG | 10451 |
rs527275143 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107651177 | CTACTGGCACCTTGA[C/T]TGTAGATTTCTTAGA | 10451 |
rs527278157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107877106 | TTAAAACCACAAGGG[A/C]AGCATCATAAACCCT | 10451 |
rs527290804 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107801776 | GATTCTGGGGGCTGC[C/T]AGATTCATGAATTGT | 10451 |
rs527312254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107870882 | AAGCAGGCCCTTCAC[A/G]CTCACCCAGAGGCAG | 10451 |
rs527312745 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963619 | AAATCATATAAAGTC[C/T]GTTCCTTCTTAAAAG | 10451 |
rs527315009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107734220 | AGGAAGCACTAAACA[C/T]GGAAAGGAACAACCG | 10451 |
rs527322200 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107660260 | ACTTTTCGAGTACCA[A/G]TGGCAACAGTGAGCA | 10451 |
rs527326392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917912 | GAGTATTTTCAGATG[A/G]GGAATGCTCAACCTG | 10451 |
rs527327628 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107828576 | TCGGATAATTCTTTT[A/C]TATGCCTGTTCCACC | 10451 |
rs527328305 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107650136 | GGAAAGAACTTGAAA[A/G]TACTTGAGGGACAGA | 10451 |
rs527333181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739317 | GGATCAAACAGGCTA[C/T]TGAAAGACTCCATTT | 10451 |
rs527334131 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657844 | AGGTGCTTCACTGGT[A/G]TTGTTAAAAATGTTA | 10451 |
rs527346195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107934182 | ATTCTTTAAATAATT[A/G]TATCCTTTAGAATAA | 10451 |
rs527354414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107606473 | AGCCACATGTCCTTC[A/G]GTTCTGAGAAATTTC | 10451 |
rs527362924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107836342 | TTAAGGTAAACAACA[A/C]AATGAAGGTGGAAAT | 10451 |
rs527381186 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107686110 | GCCTCATTACCATTG[C/T]CTTATCTTTCTTTCC | 10451 |
rs527384194 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107842283 | TGAATGGCAAGGGAA[A/G]GGAGTTGCGAGATGA | 10451 |
rs527386641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917277 | AGAAGCCCCTCATGA[A/C]ACACTGGAAATTACA | 10451 |
rs527407278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107704205 | AAGAATATATTCTTT[C/T]TGTTGTTTTTGTTAC | 10451 |
rs527428959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107883443 | ATGAATCCTGATGCA[A/G]TTTATCTCTAGGAAA | 10451 |
rs527433859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107876612 | CAACTCATCCACACT[A/G]TAACAGGGAGATAGG | 10451 |
rs527438405 | in-del | -/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107905065 | ATCAAGGAATATCAA[-/G]GAGCCAAGGTGGCTT | 10451 |
rs527440883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787868 | CCGTCTCTGCCTTCT[C/T]GACCTCAACACTCTG | 10451 |
rs527445395 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107744918 | TTGTACACATTTGCT[C/G]AAATGCTCCTGTGAC | 10451 |
rs527459525 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107782783 | AAGTATACAAACTAA[C/T]GCCAGATTCTTAAAT | 10451 |
rs527470322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710285 | ACATTGTGGCAATTA[C/T]GTAGTATACATAAAA | 10451 |
rs527471057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107703736 | CAAAGGTTGACATGG[C/T]TACCTTTTGAACTCA | 10451 |
rs527489306 | in-del | -/TT | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107790863 | CAGCTAATTTTTGTA[-/TT]TTTACTAGAGACGGG | 10451 |
rs527493906 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613155 | ACCTTTTATAGATAA[A/T]CTGTCTTTTCTCTCA | 10451 |
rs527500034 | in-del | -/A | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107673669 | ACACCAAGTCAGTAT[-/A]ACTTGTCAAAGAGTT | 10451 |
rs527509872 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107671757 | CTTGGGGAAGTTAGG[C/G]TTAGTTTGTCATATT | 10451 |
rs527519067 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107620253 | CAATGAGGAGCATGG[A/C]CCTAAATTCCTCTTC | 10451 |
rs527520806 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107663909 | TTCTATGATGCTGTG[G/T]GTTTGAAATCTTTTA | 10451 |
rs527520837 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933457 | TAGCTCACTTCAAGG[A/T]TAGCAATTAGAAGGA | 10451 |
rs527529772 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107629085 | GCCTTTTGGTTCCAA[A/T]TAGCTTACAAAACTC | 10451 |
rs527539442 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107574827 | TGAATCAGGTCTCAG[A/T]GAAGGAACACACAAA | 10451 |
rs527541006 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107935429 | CCTACTGCACAGAGA[A/C]CACAGGGTCTACTCT | 10451 |
rs527541420 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107800218 | ATATAGTCAGTAATA[G/T]AAGTGCTAGGTTATA | 10451 |
rs527548148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107855542 | CTGGGCCTCCCAAAG[C/T]GCTAAGATTACAGGT | 10451 |
rs527559462 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107716612 | GTGGATAAGCTTTTT[A/G]ATGTGCTGCTGGATT | 10451 |
rs527560629 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107635858 | TGGCCGGAATTCCTA[C/T]GTCCGAATAACAGCT | 10451 |
rs527569496 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662274 | AATTGCATTTTAAAA[C/T]ATGACAAATTGTTTT | 10451 |
rs527575076 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896234 | ATCAAATGTTAAAAA[G/T]AAATCAATTGATAAA | 10451 |
rs527579051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759492 | GTCTAAACTGATAAC[C/G]ACATTTGTTCAACAA | 10451 |
rs527586551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841989 | GCATTTATGGCTCTC[A/G]TATTTCTATTAGACA | 10451 |
rs527586562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107848226 | GCTTAGGCAGGAGAA[C/T]GGCGTGAACCCTGGA | 10451 |
rs527587140 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107946587 | AAAAAATCCAAAGGG[C/G]GAAAATAATCTGCAC | 10451 |
rs527617062 | snp | C/T | 3.35593e-05 | 0.00409616 | intron-variant | VAV3 | GRCh38.p7 | 1:107574239 | AGTAGGTTTGCAGTT[C/T]GTTAACAACCATAAC | 10451 |
rs527623869 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759006 | GAGTCTTCTATGACA[C/G]AGGCCTCTACTCAGG | 10451 |
rs527626907 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107583484 | GTCCCTGTTTGCAGA[C/T]GACATGATTGTATAT | 10451 |
rs527630568 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632059 | AATCACCACACTGAC[G/T]TCCACAATGGTTGAA | 10451 |
rs527634510 | in-del | -/GGTCATCTCCTGTCTAT | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107863416 | CTCAAGCACTTAGCA[-/GGTCATCTCCTGTCTAT]GGTCATCTCCTGTCT | 10451 |
rs527638408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903129 | TTAAGACATGGGAAT[A/G]TGCTATAGAGAAAAA | 10451 |
rs527648704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107684506 | TTCACAAGTTAAATG[A/G]ATGAAATGAGGTTTT | 10451 |
rs527660104 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107676998 | CTATATAGAAGAAAA[C/T]GAATGAGCCTCAAAG | 10451 |
rs527664062 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107799030 | CTTAAAAGTGATGAA[A/T]GCACAGCTTATCAGG | 10451 |
rs527665631 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590776 | TCAACCTCTAAGATA[C/T]ACGCAAACCTGCCAC | 10451 |
rs527674759 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107681851 | ATTTTTAGTAGAGAT[A/G]GGGTTTCACCGTGTT | 10451 |
rs527675908 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107634824 | AAAGGATATGAACAG[A/G]CACTTCTCAAAAGAC | 10451 |
rs527678893 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107954160 | CATGATAAAATAATG[C/T]TCCAAATAATAGCTA | 10451 |
rs527689610 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107634420 | AACTGGCTAGCCATA[C/T]GTAGAAAGCTGAAAC | 10451 |
rs527694792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107772527 | TTACTAGCGAAATGA[A/G]AAGACTAGACAAAAG | 10451 |
rs527705360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107582812 | TAATCCAGTCTATCA[C/T]TGTTGGACATTTGGG | 10451 |
rs527713955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107854949 | CCCTACATAGCGACC[A/G]AGCATCCATCCCTTT | 10451 |
rs527718328 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721506 | CATAAGGGCCACAAG[G/T]CTGGATACAGAAGAA | 10451 |
rs527726111 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107914165 | CAGATAGATGACAGA[C/G]AGATGAATGTAAATG | 10451 |
rs527739264 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107869029 | GTACCCAGATGGTTA[C/T]AGCTCCTTGTGTAGA | 10451 |
rs527742583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590185 | TCTTTGAAGAATTGC[C/T]ACACTATTTGTCACC | 10451 |
rs527748847 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959046 | GCGGCCTGATGACCT[A/G]AGGTCTGAAGTTTGA | 10451 |
rs527761281 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107654577 | CCCCAACCATCAATC[C/T]GAAAACTACTAACTC | 10451 |
rs527764475 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107916503 | TGAGTTCCTTCTCTG[A/T]GTAAAATATCAAATA | 10451 |
rs527765568 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107908702 | GTTAAAAGGAAAGGA[A/C]TACTGAAGAAAATGT | 10451 |
rs527773865 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107683729 | CTTCCACGTGTATAT[C/T]ATTACACTTGATAAG | 10451 |
rs527777399 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107765395 | CTTTGAATGAGATTA[A/T]TTCTATGTAAATTTT | 10451 |
rs527787460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107826833 | AAAGAAAGAAACAAA[C/T]GGAAAATAAAGGGTG | 10451 |
rs527796141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107909537 | CCCATTTTAATCCAA[C/T]TGGTACAGATTAATC | 10451 |
rs527799435 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107853627 | TCTTTTAATGTCTTT[-/A]AAAAAAAAAGTTATT | 10451 |
rs527804526 | in-del | -/A | 0.0942524 | 0.195557 | intron-variant | VAV3 | GRCh38.p7 | 1:107960466 | TAAGACTCCGTCTCA[-/A]AAAAAAAAAAGAAAA | 10451 |
rs527815596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771888 | ATGGGCTGTCAGCCT[A/G]TGCAATGGTTAAACC | 10451 |
rs527816149 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702303 | GAGAACAGCGTGGAG[A/G]AAATCCCATGATCCA | 10451 |
rs527818509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107960910 | ATAGCACATTATAGA[C/T]AAATATATAAATAAT | 10451 |
rs527820409 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690919 | TGATCATGCTGAGTG[G/T]GCCACATAAATAGCA | 10451 |
rs527849124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107779289 | CAATTAATTTCAAAC[A/G]TGTACGGGATACTTA | 10451 |
rs527862128 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107596433 | ATACAATAAGGATGA[A/C]CAATTTAATGCTAAA | 10451 |
rs527864046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107604257 | TGTATAAACATCCAC[C/T]TGTAATGCAAACTTA | 10451 |
rs527867687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107648657 | ATTACACAATTTTAC[A/G]GAGTATTGTCACCTA | 10451 |
rs527873765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875138 | AGCCTTTGAAGTTGC[C/T]TTTCAATTACTCATT | 10451 |
rs527886737 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786425 | AAGGTAAGGACGGGA[A/G]TCAAGATGATCAAGG | 10451 |
rs527910973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732542 | ACGGTCTTAGCAAAC[A/G]GCACACCAGGAAATT | 10451 |
rs527930197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915756 | GAATCCAGTAAGTCT[C/T]TGATTAGTGAATGAA | 10451 |
rs527933220 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656661 | TGGTAGATATCCCAA[G/T]GAACCCTGATGTGAC | 10451 |
rs527937235 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662784 | AGACATATTAGTCAT[A/G]TGAATAAGGGGCAAA | 10451 |
rs527942787 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107931488 | GATAACCTAGATAAC[C/T]GTTGAATCCAGGTGA | 10451 |
rs527952307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603765 | TTTATTTGCTAAATA[C/T]AGGCAAGCCCAAAGC | 10451 |
rs527957958 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107841139 | CCAATAGTGAATGCC[A/G]TATGGTCTTAAATTC | 10451 |
rs527963744 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107915521 | GAGTAAGTTACTTGA[A/T]CTGTTCCTCGATGTC | 10451 |
rs527972190 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737428 | CAGGCAACCTACAGA[A/T]TGGAAGAAAATTTTT | 10451 |
rs527975312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744109 | TCAGGCAGGGGCTGC[C/T]GCTCCGGATGACCAA | 10451 |
rs527986070 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107810437 | GTCCCTTTCCAGTCA[C/T]ACTTTCAATTCCACA | 10451 |
rs527990283 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107604687 | GCATCTTGTACTACC[C/T]ACTCCATTATTCTCA | 10451 |
rs528014180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107743302 | AGACATGCAGAAGAC[A/G]TAAACCAGGGGTGGC | 10451 |
rs528016382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107751046 | TTCACACTGGAAAAA[C/T]TGTCTTTAAGGTTTT | 10451 |
rs528023662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881754 | TAAATCAGGCCAAAG[C/T]TCTCTGGATTAGAAA | 10451 |
rs528023754 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107793026 | CCAAACAAAAATGAC[A/G]ATAAATAAGTGTCAT | 10451 |
rs528044349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900307 | AGCCACACGTCAGGA[C/G]GAAGTTACCTTTATG | 10451 |
rs528047679 | snp | C/G/T | 0.0249056 | 0.109201 | intron-variant | VAV3 | GRCh38.p7 | 1:107681811 | GGCACCCGCCACCAC[C/G/T]CCCAGCTATTTTTTT | 10451 |
rs528055979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719497 | CAGAGAAATGCAAAT[C/G]AAAACCACAATGAGT | 10451 |
rs528066940 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107631957 | GTGCATGTACCTTTA[G/T]AGCAGCATGATTTAT | 10451 |
rs528082183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746367 | TCCCAATATCTGCAT[A/G]GACATTCAACGGAAC | 10451 |
rs528084109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858919 | GATAAATCAGAATTC[C/T]AACATTTTTGACAAA | 10451 |
rs528086337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107803868 | AGTCCATGACTGTTA[C/T]TTTATTGCAATCTAT | 10451 |
rs528097772 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587655 | GAGTGCAGTGGCACC[A/G]TCTTGGCTCACTACA | 10451 |
rs528110456 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943866 | ACTAAAAATGTCAAA[A/C]CCCTTCCTAAGCCTC | 10451 |
rs528111175 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107578658 | CTGTTGCCCAGTTTG[C/G]AGTGCAGTTACACGA | 10451 |
rs528114367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107952036 | ATATGTTCACTACAG[C/T]ACTATTCACAATAGC | 10451 |
rs528114445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107718870 | AGAGATATAGACCAA[A/T]GGAACAGAACAGAGG | 10451 |
rs528121166 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107620227 | TATAACTCAATCTGA[C/T]AGTTCCCTGTCAATG | 10451 |
rs528123338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107851311 | CTGGCCTTAAACAAA[C/T]GTGTTATAAAAGGGT | 10451 |
rs528125249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731499 | TTTCCAGGTAAGGAA[A/G]AGTTAGATAGGTTCT | 10451 |
rs528126679 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107724913 | CAGAAATCTGATCTT[C/G]TTCTGTGGCCAAGGA | 10451 |
rs528132888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107587080 | CTAGATACAAGAAGA[A/G]TTTCTCTGGCATTCC | 10451 |
rs528133021 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858132 | AAGTGAGTTAACCAC[A/T]CTTAAAGATATACCA | 10451 |
rs528133067 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903174 | TATTTAATTTTTTAA[A/C]AAAATCTGAGCAGTT | 10451 |
rs528146316 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107816183 | TAACAGAAAGGCAAT[G/T]TGATGTATAAACAAA | 10451 |
rs528146344 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107682371 | ACAAAAATATTATGT[C/T]CACAGTCATATACCC | 10451 |
rs528148072 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107744493 | CCCTTCAAAAAACAC[C/T]ATGAAGGCTAATTCT | 10451 |
rs528152255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913722 | TACACAGGAATCATC[A/G]ACCTTGGCAGAGTGG | 10451 |
rs528153837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107957931 | TCTGGCAAGCCATGG[C/G]ATTGTACCTCACCAA | 10451 |
rs528173548 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107934575 | AGGAGGAACGGCTCC[C/T]ATGAAAAGTATAGTT | 10451 |
rs528175440 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107681590 | AGTGTTTGGGTTTTT[C/T]ATTTCCAAAAATATG | 10451 |
rs528182549 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107823631 | AGTCACGAGACTGTC[C/T]GTTAATGGACCAAAT | 10451 |
rs528187137 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107761897 | TCCAAGATTTAGAAG[C/G/T]CTTGGATTGTATTTA | 10451 |
rs528193547 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107809842 | AATTTACAAAACAAC[-/T]TTTTCTTTTTGTACA | 10451 |
rs528193771 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107911001 | AAAAGAAAAAAAAAA[-/T]GAAAAAAAAAGCAAG | 10451 |
rs528218620 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866637 | ACCAGCTGGGCCAAC[A/G]TGGCGAAACCCCATC | 10451 |
rs528223397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694426 | AGCATTCTGTGAATT[A/G]CTTCATTTTCTTGCT | 10451 |
rs528226631 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769278 | TAGAAAAACAAACAC[C/G]CTGATCAAGTCTAAC | 10451 |
rs528256188 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107600821 | CTAAATTCATTGGCC[C/G]TTTTCAGTGACGATT | 10451 |
rs528276142 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107645457 | GAAACAAGGGCACAG[C/T]GATATAATGAATTCT | 10451 |
rs528279568 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107714276 | AGTATTTCTTCTTCC[C/T]TTAGAATTACCAATT | 10451 |
rs528282436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872111 | CACAGACAGTGGACA[A/G]GAAAAACAGGACTGA | 10451 |
rs528288800 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107761200 | CAAGACCATCCTGGC[C/T]AACATGGTGAAACCC | 10451 |
rs528290139 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964929 | GATGCGGCCGCCGCC[G/T]CCGCCGCCGCGGTTC | 10451 |
rs528292417 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107783433 | GGAGGAGTGTTCAGG[A/T]ATAGTAGCTGATGCT | 10451 |
rs528308382 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107899598 | GGACAGGAAAGAGAA[C/T]GAATTCATTGGAATT | 10451 |
rs528310223 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107653135 | TGCAGACAGGGTTTA[C/T]TGATTTATAAGCTAA | 10451 |
rs528319190 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107939168 | TTTTTTTTTCTAAAC[A/G]CTAAGATAACAGCGC | 10451 |
rs528335830 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107653484 | AAACTTCTATGAGTC[C/T]ACTTTCAAACTCTGA | 10451 |
rs528338084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107735429 | CAAGAGCTGGTTTTC[C/T]GAAAAGATCACAAAA | 10451 |
rs528338356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702419 | GCATAAGGGAAGAAA[C/T]CAATACTTACAAAGG | 10451 |
rs528353393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107927908 | CCTGCTGATGGTAGG[A/G]CACCAGGGCCTTGAA | 10451 |
rs528372882 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857226 | CAGGCAGAAAAACAC[A/G]AAAAGGCTACACTGG | 10451 |
rs528401153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107706158 | GATATGCTCCGAGAC[A/G]TTACACGCAATTTGA | 10451 |
rs528409059 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659152 | GGAAGGGATCCAGTT[A/T]CAGCTTTCTACATAT | 10451 |
rs528416366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107789895 | AGTTACAGCTCATGT[C/T]AATACAGACTAGCCA | 10451 |
rs528427979 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107790877 | ATTTTTACTAGAGAC[A/G]GGGTTTCACCATGTT | 10451 |
rs528432850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107935516 | GGTCTGACAAATACA[C/T]AAATTTGGTCCTCAG | 10451 |
rs528439972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891788 | AGGTTGCAGTGTGCG[C/G]AGACCGCGCCATTGC | 10451 |
rs528440978 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107911003 | AAAGAAAAAAAAAAG[-/A]AAAAAAAAGCAAGGT | 10451 |
rs528451958 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795872 | GTCAAAAGTGCTGAG[C/T]TTATTAGAAAGTAAT | 10451 |
rs528453947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107789385 | TGGGGAACATGCCAT[A/G]GATTTCCAGCCCAAA | 10451 |
rs528470417 | in-del | -/GCGTGCGTGCGCGCGCGCGCGCGCACAC | 0.366885 | 0.220993 | intron-variant | VAV3 | GRCh38.p7 | 1:107574993 | TGTGTGTGTGTGTGT[-/GCGTGCGTGCGCGCGCGCGCGCGCACAC]GCGCGCGTGTTTAAT | 10451 |
rs528480547 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107705714 | ATTTACTCTGTGCCA[A/C]AGACTGTGACAACCA | 10451 |
rs528483224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942782 | TTTCTGGTTTGCAAT[A/G]AGATTACTGACTTGC | 10451 |
rs528483824 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107878116 | AACAATTGCAACATA[C/G]TGCCATATATGCTTT | 10451 |
rs528496983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885335 | TATGCTAATGGCAGA[C/T]TAATGCTAATGTTAC | 10451 |
rs528497021 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107835035 | GCAAAATGCTCTAAT[A/C]AGCACCCATCATTCA | 10451 |
rs528500620 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572488 | ATCTGTTTCTGTAAA[C/G]AATGCCAGCTTCTTC | 10451 |
rs528512634 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107926980 | GGCAACTAAGGGAGT[A/G]CTTGTACCACACCCC | 10451 |
rs528514288 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107935547 | TCCCTAAAATTAGAA[A/T]TAAGTTTCCCCATCA | 10451 |
rs528526179 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107614147 | AGAGCTCCTGGAATC[A/G]GGGATATACCCAAGT | 10451 |
rs528527505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107622523 | TTCCCTGTGGCTCAT[C/T]TATCCCCTTAATACT | 10451 |
rs528535287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747098 | TTGGCCAGGCTGATC[C/T]CGAACTCCTGACCTC | 10451 |
rs528547249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802263 | TTTTTGTGGACTCTT[C/T]AGATTTTTCTAAATA | 10451 |
rs528556698 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107898443 | TTCCACCACAGCCAG[A/T]GGCCTTCTGAGTGAA | 10451 |
rs528562435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673225 | GGTGATCTTTTCAAC[C/T]AGTCCTAGCTGCCCA | 10451 |
rs528564022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107754299 | ACTATATGAAGAGAT[A/G]ATGAGAGGCTACTGT | 10451 |
rs528571251 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107577476 | CATTGGGCTATGTTT[G/T]CCTAGAGAGAAGGCT | 10451 |
rs528575415 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107665679 | TAGTTTTACATACCT[G/T]ACTGCACACAGCCAT | 10451 |
rs528578876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700244 | TTCAACTTCCTTATG[A/G]CCTGAAGACAAGTGG | 10451 |
rs528584435 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107616288 | TCATGCCCTTTGCAG[C/T]AGCATGGGTGGAGCT | 10451 |
rs528602983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107843525 | AAAATGTATGTGTGC[A/G]TGTGTGTGTGTGTAT | 10451 |
rs528609715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586109 | TGTAAGCCATCCCTC[A/G]GCGCTCATGAGTACC | 10451 |
rs528616296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107897813 | CTTTATGAAATGAAA[G/T]GGATAGTACACATTA | 10451 |
rs528616411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107768382 | GATCTGGAACCCCCT[A/C]AGGAAATGAAGATTT | 10451 |
rs528617348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107621591 | CTTTATGTGATGATA[C/T]GAGGTTTTTACTAAC | 10451 |
rs528657350 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107793133 | AAATGCTCAAGACAA[C/T]CTTATGAACAGAATA | 10451 |
rs528673337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717793 | AGTCCTGGATATCCT[C/T]ATTAATCTTCTGTCT | 10451 |
rs528673624 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107724088 | GTATAGAAATTAATA[A/T]GTGAGTCATGAAGAA | 10451 |
rs528675712 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107856505 | CATGAAATTTTAAAT[A/G]GTACTTTTCCCCCAG | 10451 |
rs528678019 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107801717 | CTTGTCTATAAATTT[A/G]TTCTGACCACAAGGC | 10451 |
rs528681213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864365 | GGTGGCTCATGCCTA[C/T]AATCCAAGCACTTTG | 10451 |
rs528685089 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808490 | ACTACTAGAAAAAAG[C/G]AAATTTTATAGTATA | 10451 |
rs528689156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636560 | GCTCAAAATAATTAT[A/G]TTAGCCCACAGTTGG | 10451 |
rs528695724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948569 | ATAAAGCTGGCCAGG[C/T]GCAGTGGCTCATGCC | 10451 |
rs528703484 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107585447 | GCCCACATCCCTCCA[A/G]TGGTTTCCTGTTTCT | 10451 |
rs528716621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808026 | ATTTTCATAAACCTG[A/G]CCAATGATGATTGAT | 10451 |
rs528717437 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833491 | AGAAAATATTATCAC[A/G]TATTTGTTCAAATCT | 10451 |
rs528717706 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107857066 | GTGATTGGATTGAAG[G/T]ATGCAAAGTTTTCCT | 10451 |
rs528725722 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107643568 | GAGGTCCACTCATAA[A/T]CATGATATTTTTTGC | 10451 |
rs528732756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107949634 | AAGTACCCAAATCTT[C/T]TGTGTTACCACTCAT | 10451 |
rs528736081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729340 | CTACATAAGGCAAAT[G/T]TGGTATATGATAATA | 10451 |
rs528736681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107723640 | CAACTTAGCAGACCC[A/G]ACTCTCTCTCCCTTG | 10451 |
rs528739092 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107863830 | AGTTTGATTTCAGTT[C/G]TCAAACCAGATTTCC | 10451 |
rs528750651 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954115 | TGGCTTTAACACCAT[G/T]AAGGGTCTATGTTAA | 10451 |
rs528751974 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767779 | TTGAATCTTGCCTAG[A/C]ATTACCTCACTTGGC | 10451 |
rs528768808 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686225 | TCCACTCCAGAATGG[C/G]ATGTGAGATGTACAG | 10451 |
rs528771621 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107647462 | AGCAAGGGAAAGTAT[C/T]CTGCCTTCAAACAGC | 10451 |
rs528793315 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107734939 | ACACTTATTCCAAAA[C/T]TGACCACATAGTTGG | 10451 |
rs528798462 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107904571 | CCTGCATTTATTTCT[G/T]CCCCCAACCACTGTG | 10451 |
rs528807116 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107810839 | AACAGAAACAATACG[C/T]GACAGGACCAGTTGT | 10451 |
rs528819699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107630207 | TCTGATCATTCCTTA[C/T]ATCATGGAGGCCTCC | 10451 |
rs528831315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107685443 | AGGATTATTAAGTGA[C/T]AGATTATTAGCTTTT | 10451 |
rs528845131 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906049 | ATTGTAAAAGAAAAA[G/T]CTCCTAAATTTAAAG | 10451 |
rs528850607 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769203 | TCCTAACCGAGTTTA[C/T]ACTCCATGAATCACT | 10451 |
rs528856414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107957323 | CCTCCTTTCTCTGGC[C/G]TTATCTTCTGTTGAA | 10451 |
rs528859147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586422 | AACTAAACAGTAAAT[A/G]AGGAAAGAAGTGCTT | 10451 |
rs528859374 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107680801 | GAGGAAACTATGGCA[C/G]AGAGAGAGGAGGCAA | 10451 |
rs528860955 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107784923 | ACAGTGTTGTCTATT[C/T]ACTCAAACCTAGAGC | 10451 |
rs528864180 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594177 | TTTTGAGTTGCTTTA[C/T]GAGGGAGATCTTACC | 10451 |
rs528868620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107957809 | ACTGTATTTGAAAAT[C/T]AGAAAATATGTGGTG | 10451 |
rs528871211 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107638270 | GAAGAATAAAACATG[C/G]TGTCTATATTACAAA | 10451 |
rs528882863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107645391 | TGTCAGCACTTCCAA[C/T]TTCAGCATGATCTGT | 10451 |
rs528888048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858033 | TCCTGAACAAACTAC[A/G]ACCACTCTGGCAATA | 10451 |
rs528904610 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776130 | CCTGGTTAGCACACA[A/C]ATGGAAACTCAGTAA | 10451 |
rs528911474 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107730023 | CCATCGACCAATGGA[A/T]TAGTCTGGCTACTTT | 10451 |
rs528918325 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815588 | TGTCTGTTTCTGTGG[C/T]TTACAAATAAGAATC | 10451 |
rs528923296 | snp | A/C | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588882 | ATAAAATATTTAATA[A/C]AATGTTTCAGACAAA | 10451 |
rs528925462 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952177 | ACATGGATAGCGCTG[A/G]AGGCCATTATCCTTA | 10451 |
rs528927976 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107822657 | GACTCCATCTCAAAA[A/T]AAATAAATAAATAAA | 10451 |
rs528934417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872007 | CAAGTAACACATCAC[C/T]TGTGTTTTTTAATTT | 10451 |
rs528937364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864485 | AAAATTAGCTGGCTG[C/T]GGTGGCATGCACCTG | 10451 |
rs528943264 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923874 | CTTCCATCTTGTAAG[C/G]ACACAATGAGAAGGT | 10451 |
rs528944923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107644651 | TCTTTATTGCCAACA[C/T]GCCCAAGTCAATCAT | 10451 |
rs528951964 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107735820 | AACTATTCCAATCAA[C/T]AGAAAAAGAGGGAAT | 10451 |
rs528959292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107919503 | AGAATTTATCTTCTA[C/T]AAGACTATTGTTTTA | 10451 |
rs528961973 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107870005 | GCTGAGTAGTATTCC[A/G]TCATATATACAATTT | 10451 |
rs528990972 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107735404 | AAACCCTTCAAAAAA[C/T]CAACGAATCCAAGAG | 10451 |
rs528999505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912782 | CAACTGCAAACTTGG[C/T]TGACCCTTAGGAACC | 10451 |
rs529021737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964515 | CCAAGGTAGGAAACG[A/C]CAAAGTGGTGCCGAA | 10451 |
rs529032606 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107694001 | TGGCAAAGTCACAAG[A/T]TCAAACTGATCTGGG | 10451 |
rs529044213 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107608437 | TCAGTTTGATTATCA[A/G]TGCTATCAGCTCTAG | 10451 |
rs529046287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599807 | CCTATTGTGTTTCAC[A/G]GATAGAAGAGTAAAC | 10451 |
rs529046716 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107878963 | AGTATTCTTTTGTCA[A/T]AAAACAGAAAAAAAG | 10451 |
rs529056238 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107906380 | GTATAAAATAACAAA[C/T]CGGGCTGGGCACGGT | 10451 |
rs529075611 | in-del | -/CATATA | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963608 | ACATACTTATTAAAT[-/CATATA]AAGTCCGTTCCTTCT | 10451 |
rs529076071 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107705563 | TTAGTGTGAACATTA[A/C]AAAATTCTTAACATT | 10451 |
rs529100029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107829676 | TATTTACTTTAGCCT[A/G]AGACATCCACCTAGA | 10451 |
rs529104616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107615402 | ACTGGCTAGCCATAT[A/G]CAGGACTGAAGGTGA | 10451 |
rs529112720 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107864459 | AAACCCTGTCTCTAC[-/A]AAAAAATGCAAAAAT | 10451 |
rs529133196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739820 | CACATCCAGCTCATC[C/T]AGGAAGGCTCCCCCT | 10451 |
rs529140505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107658970 | TAGATCCCATTTGTC[A/G]ATTTTGGCTTTTGTT | 10451 |
rs529142194 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795533 | TATCTCCCCTCCCCC[A/C]AGGAAAAAAAATGAA | 10451 |
rs529152052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760423 | GAAGAGGTCTAATAT[A/G]ATTAATCTGCCAAAA | 10451 |
rs529159489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739464 | TAGATTCAGGGAGAG[G/T]TGAGCTGGCTTCAAC | 10451 |
rs529160953 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107617964 | AGGGATGTGGGGTGA[A/G]GTGAGGTGGGTGCTG | 10451 |
rs529164367 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107843475 | TTCACTAATCATCTA[C/T]AGACTTTTGTCTTAG | 10451 |
rs529184258 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107747004 | CCTGCTTCAGTCTTG[C/T]GAGTAGCTGGGACGA | 10451 |
rs529197180 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107836516 | CTGCACCTACAGGAA[A/C]TGGAAAAACAAGAAC | 10451 |
rs529200364 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107587008 | CTTCTCAGGAGTGTT[A/C]CAGAACGTTTAAAAA | 10451 |
rs529201167 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107739946 | CACAAATGGTATTGC[C/T]GCTGGGAAGAAAATG | 10451 |
rs529207156 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898829 | TCTTTTAAACTATTC[C/T]AAGCAATGTAGTTCC | 10451 |
rs529222880 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746411 | AAACTACTTCTACTG[G/T]TGTGTTATTTTATTG | 10451 |
rs529225029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107754179 | CACTGAGGACCTTAA[A/G]TATCATGCCAAGGAA | 10451 |
rs529237212 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107748642 | AAATATAGTTATTAC[A/G]TAAAAAGTTTATCAT | 10451 |
rs529241791 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107884534 | CAGCCTCAATCTGAT[A/C]TCATGTGCTCAAGTG | 10451 |
rs529248173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711246 | TGTGTAAGTTTCTAA[C/T]GCTCTCTAGCAAAGA | 10451 |
rs529260675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753317 | AGGGAAAGAGAAGAA[C/T]GGGAAGTTCATGTTT | 10451 |
rs529262026 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107898269 | TTCTGGGTAGTGAGA[A/G]TTCCTCTTATTTCTG | 10451 |
rs529264901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107941468 | GAACTCTAGAAGATT[C/T]GAGAACTTCTTTTGA | 10451 |
rs529265259 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107795060 | GAGGAGGGCACTGAA[G/T]TCCCAAATTCTTTCA | 10451 |
rs529265464 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107576685 | AATACCCACTCCACA[G/T]TGCCATCTTTGAACC | 10451 |
rs529280776 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107949480 | AGTGCCCAGCTAATT[A/T]AAAAAATAATTGTAG | 10451 |
rs529303124 | in-del | -/T | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107939152 | GTTAAATTTGTCTAG[-/T]TTTTTTTTTCTAAAC | 10451 |
rs529310881 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842975 | TATGATGAGAGCAGA[A/C]GCAGACCTACTGAGA | 10451 |
rs529313699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807894 | CAGAAACTGATCAAA[C/T]GGTACTGTTTCTCTA | 10451 |
rs529316282 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942026 | TCCTGCCTCCCCTTA[C/G]AGTCTGAACTCCAAA | 10451 |
rs529318257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672701 | CACCAAATCTTGAAT[A/G]GAAAGAGGGAGTAAG | 10451 |
rs529323069 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948445 | CTTGGTCAAACCATT[G/T]TATACATATCAGAGG | 10451 |
rs529330170 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107917919 | TTCAGATGAGGAATG[C/T]TCAACCTGTATGAAT | 10451 |
rs529339175 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107679524 | TAAATGCAGGATGCT[A/G]TGAGTTCCACAAATA | 10451 |
rs529345490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107904495 | CTTTTCTTATTTGAC[A/T]GCTCCATGTTTCTGC | 10451 |
rs529351315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807279 | TTGAAAGAGTAGAGC[C/T]GGAAGCCACAGCAAC | 10451 |
rs529359998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107723555 | ACAGGATTCCAGAGT[A/G]ATGTTTCCAGCTTCT | 10451 |
rs529381241 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636385 | AGCAATCTATAAGAA[C/G]AAACTGAAAGAGCAA | 10451 |
rs529388425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107584616 | AAAAACTAGGAATAA[C/T]TTAGATTAATTTCAT | 10451 |
rs529401176 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107579452 | CTGCAAGAACTCTCC[C/T]GTTCTCTCTGTGAAC | 10451 |
rs529408499 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910902 | GGAGAACCGCTTAAA[A/C]CTAGGAGGCGGAAGT | 10451 |
rs529412753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107685349 | GAGATAATACTAGCA[C/T]TGACTTCATAGGTTT | 10451 |
rs529416598 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107808401 | AGAGTCACACCCTTT[C/T]TCAAATTGCTTTTCA | 10451 |
rs529435454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107846812 | ACTTAGACTCCCACA[C/T]AATAATAGTGGGAGA | 10451 |
rs529449414 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107723052 | ACTATAGACTTCGTC[A/T]TGTTATTGTGTAATT | 10451 |
rs529462799 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107716553 | ATTCATTTGCATATG[C/T]TGAACCAGCCTTGCA | 10451 |
rs529467124 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107614244 | TTTATGAACCGCCTG[C/T]GTTTTCCTCAGTTCT | 10451 |
rs529483248 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107870782 | ATGAAACTATCCTAT[C/T]GCAATTCAAATCAAC | 10451 |
rs529491664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729274 | TTATTAATGTACTAT[C/T]AGAGAACAGATCCCT | 10451 |
rs529491897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107642829 | TGAACTTTACAAAAA[A/T]TGTCATTATTAACAT | 10451 |
rs529497842 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635597 | GCACGTTGTGCACAC[A/G]TACCCTAAAACTTAA | 10451 |
rs529501601 | in-del | -/AAG | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107726254 | CTATAAAAAGAAAGA[-/AAG]AAATTGCTCACAGAA | 10451 |
rs529528027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590938 | CAGTGGTCTTTTAAG[A/G]CAATGTAAATTAGTT | 10451 |
rs529554071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728673 | AAAACCGTGTCCCCA[A/G]ATCAGCTCTACAAAG | 10451 |
rs529555541 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107650024 | ATTTAAGGGTAGGCC[A/C]TCAGGTCAGGGTTAA | 10451 |
rs529576407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107692865 | CATTATACCAAAGTC[A/G]TTTGCTCCAACAGTA | 10451 |
rs529590599 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871119 | ACGGAAACGAACAAA[A/G]TTACAGATACTGTCA | 10451 |
rs529605653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107895145 | AAAGAGCTATGGGAA[A/G]CAGGAGCAGGAACAC | 10451 |
rs529606465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864063 | AGAAGAGCTTATATA[A/T]AAACAAAAGGTATGA | 10451 |
rs529624765 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107827783 | TGAAACAGTCTTATT[C/T]CTGTGAGTGATTAAA | 10451 |
rs529638548 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107801063 | TCCCAGTACTACTTA[C/T]TAAAGAAACCACCTT | 10451 |
rs529641061 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833878 | CTTCCTTGACTACTA[A/C]AAGTAATCAAGCACT | 10451 |
rs529649936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107962186 | ACAGAACGACTCTCA[A/G]ACATACCAAAACGCC | 10451 |
rs529650588 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107704165 | ATTTAAAAGAATAAA[A/G]AGGAAATTTAAGAAC | 10451 |
rs529656783 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107893698 | TTACCTCCCACCAGG[-/T]CACTCCCACAACATG | 10451 |
rs529658875 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107573442 | AGGATTCTACAAACA[A/G]AGTATTTTGTTTTCA | 10451 |
rs529659316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107798313 | GTGTAAAAATAGGAG[A/G]GGTGTTCTCACACCT | 10451 |
rs529674069 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107792425 | TGATCCTCCCACCTC[A/G]GGCTCCTCAGTAGCT | 10451 |
rs529676434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750329 | AATATTTCTTTTTTC[C/T]TATTAAGAACAACGT | 10451 |
rs529690417 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107707682 | ATTATTGAAGTGTAA[C/G]AGGGTAACTCAAGAG | 10451 |
rs529713520 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107676092 | GAAACTTGTTGCACA[A/C]AATAATAGATGTACA | 10451 |
rs529715874 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107705451 | AGCAGGTGAGGGTAG[C/G]AGGGAGAAGAGGGTC | 10451 |
rs529722918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720791 | GAGACAAGGCCCACA[C/T]ACATCAACAATTTGT | 10451 |
rs529728756 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107675838 | CCATGACAGGGCTAC[A/G]AGAAGATCAAATATG | 10451 |
rs529729782 | in-del | -/A | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107907433 | CAAAAATTTTAAGAT[-/A]ATATGTATAACTGCT | 10451 |
rs529740030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107675516 | TGCTATTATGCATGA[A/G]TATGTTTAATACAGA | 10451 |
rs529741760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107682796 | TTTATCATCAAGTTC[A/G]TGTATTTGGAATCCT | 10451 |
rs529746516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945264 | GATCTTATTTAATTA[C/T]AAGATACATTTGAAT | 10451 |
rs529751170 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107757411 | TTTTTACAAATAAAC[C/G]ATTATTATTGGTTTT | 10451 |
rs529756163 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107846640 | TGAGTCTCTGACAAA[A/G]CAGACTTTAAACCAA | 10451 |
rs529763823 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107714766 | TTCACCTATTCCTTT[C/T]CTTATATTCCAAATC | 10451 |
rs529775666 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107824859 | ATAAAAATATAAAAA[G/T]CAATATTAACCAAAA | 10451 |
rs529785215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107764394 | CTTACAGAGCCCTAT[C/T]ATACAGTGCTTATCA | 10451 |
rs529786487 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107668452 | GCATAATACCTCTCA[C/T]AGCTTTGTTGTGAAA | 10451 |
rs529791814 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107771751 | GTTCACCCCATCAGC[C/T]GAGTGAGGACTGCCC | 10451 |
rs529793515 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107580461 | CCTATTAAATACTGT[A/T]TGTCTCACGGCATTA | 10451 |
rs529817734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107846012 | ATCAGATCCCCAAGG[C/T]AGAAATGAAGGAAAA | 10451 |
rs529822947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702691 | TATGTCCTTTTAATG[C/T]CATACTTGCGTATTA | 10451 |
rs529828466 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588414 | TTTATAAATATACTT[A/T]AAATTGTCAAATGAG | 10451 |
rs529829158 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107864146 | AAAGCAAAACATTAC[C/T]TTACAAAATGCAATG | 10451 |
rs529831547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107756858 | CACCAGCTGGCCTAC[A/G]ACTTACACAAGCCAA | 10451 |
rs529832961 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107804464 | CTTGTAGACATAACA[A/T]GTCATTTTACAGAGA | 10451 |
rs529838139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107867736 | GTACTCCTTGCCAGG[A/C]TGAGCCAGCTCTAGG | 10451 |
rs529838427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624980 | CTGTGAGGTGATAAT[C/T]TGATAGGATTAGGGA | 10451 |
rs529844147 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107811422 | TGACGCTCTGGAAAA[A/G]CCTCACATAGAAAAG | 10451 |
rs529844834 | in-del | -/AT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107930335 | AATTAAAACTAAAAA[-/AT]TTTTTTAAAGAATTA | 10451 |
rs529858571 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107585368 | TTTCATGGTTTTTTT[A/T]ATTATAATACAGAAA | 10451 |
rs529869155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107763836 | CAAAACAGTGAAGGG[C/T]TTCTGATTTGAAAAT | 10451 |
rs529876432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860784 | ACTTGCAGTCCCGGC[A/T]ACTCAGGAGGCTGAG | 10451 |
rs529904574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632779 | ATGCATACTTGCTAT[C/T]TGAAATAAATGTGTT | 10451 |
rs529910880 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107647275 | CCTTTCACCTCTGAG[G/T]CCCAATTTAAAATCT | 10451 |
rs529914615 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959585 | TCCTACCTCATGGCC[A/G]TTGCCTCTCAACTCC | 10451 |
rs529919188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107827280 | CACTTAGTTCTTCCC[C/T]TCTCTCAAATCCCTC | 10451 |
rs529932343 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107810786 | CCTGAGATCATCCCA[C/T]AATGAACAGTAAGAA | 10451 |
rs529933393 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689540 | TTTTTCTTTTTTTAA[C/T]GAATACTTCTGATTA | 10451 |
rs529945842 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107852399 | TTGTAAAATAGAAAA[A/G]GAATAAAAACCACCT | 10451 |
rs529952380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107817678 | ATCCATAGGCAGGGG[A/G]GTGAGGAGGCAAGGA | 10451 |
rs529955254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736858 | AGAAAAAACTACTTT[A/C]AAGTTCATATGGAAA | 10451 |
rs529956560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726116 | ATGTGTGACAGCCTA[C/T]CTTCAGGATATTTGA | 10451 |
rs529958897 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914807 | GGGAGACAGAAAAGA[A/T]AAACAAGATTTGGTC | 10451 |
rs529967827 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587794 | ACGGGGTTTCACCAC[A/G]TTGGCCAGGCAGGTT | 10451 |
rs529974530 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107817119 | CTCTTGCTCTGAAGG[A/G]GTTCACTACTTACTG | 10451 |
rs529978338 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107914226 | GGGGACAAACTCAAC[C/T]GTGCCAGCAGAGCCA | 10451 |
rs529978955 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966573 | ATATTTCTGTAGCCC[A/C]AATTTTTTATTACGA | 10451 |
rs529981327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777511 | GCTGTAACACCTGCC[A/G]CCTGAAATCATCTGA | 10451 |
rs529982133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | VAV3 | GRCh38.p7 | 1:107595703 | TAGCACACAGCTCAT[C/T]CTGAAAGAAAGTGGC | 10451 |
rs529991521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107695844 | AAGGCCTAAATGTGA[C/T]GTGCCATGGATCTGT | 10451 |
rs530014252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880523 | ACTGGAGGCCAGATG[C/T]GGTGGCTCATGTCTG | 10451 |
rs530015233 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907453 | GTATAACTGCTATCA[G/T]TTAAATGTGTCCCCC | 10451 |
rs530018569 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777096 | TTGTAAAGCTTTCCA[C/T]CGCCAGTTTAAGGTT | 10451 |
rs530020783 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595029 | TGGTAGGAAAATTGT[G/T]TTTTTGGAGAAAACT | 10451 |
rs530026911 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107660087 | TTCCCACGGATCATC[C/T]AATTCACCTTCAATT | 10451 |
rs530028345 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107752405 | TACAAGAAAATGGGG[-/A]AAAACTTTATGACAA | 10451 |
rs530029913 | in-del | -/T | 0.00240336 | 0.0345819 | intron-variant | VAV3 | GRCh38.p7 | 1:107792225 | AGCAAGTGTTGAGTA[-/T]TTTTTTTCTTACATT | 10451 |
rs530033039 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107731628 | TTCTATAGTAAAATC[G/T]TCTTCATTATAAGGA | 10451 |
rs530053238 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688841 | AATAGCAAATTATAC[A/G]TAGTACAACATTTCG | 10451 |
rs530059552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107791239 | TTGCCAATAGCCTTG[C/T]GTGCCCCATTAAACT | 10451 |
rs530067848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107609745 | TGCACACACACCCCC[C/T]TCGCAGATAAAGATA | 10451 |
rs530079479 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107639481 | AAAGCCAAATAATAA[A/G]AAAATGCATGGCTCA | 10451 |
rs530081158 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107654305 | ATAGCTTTTATAGAC[A/G]ACAGTAAATCCTTTA | 10451 |
rs530082220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107646318 | TCTTGGGAAAATACA[A/G]ACCCAACAATTGTTT | 10451 |
rs530084164 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107637714 | TAGTAAATTCTACGA[A/C]ACACTTCAGGAAGAA | 10451 |
rs530085995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107626098 | GTATATTATAACCTA[C/T]ATTGCACTGTACCAA | 10451 |
rs530087837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832543 | CATTTTCATTTCTAT[C/T]TGAGTCTTTTATAAA | 10451 |
rs530090645 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107823668 | ATCTCCACAAAACTC[C/G]TATGTTGAAGCCCTA | 10451 |
rs530108225 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107601639 | ACTACCAAACTTGAG[A/T]AACATACTTGAGACC | 10451 |
rs530108629 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107678059 | AAATGACTACAAGAA[A/G]ATCAACTGTCCTAGT | 10451 |
rs530121797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107839554 | AAAATTTATAGCATT[A/G]AATGCATATATTAAA | 10451 |
rs530126225 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107783924 | AATTAGCCAGGCATG[A/G]TGGCGGGCACCTGTA | 10451 |
rs530145360 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107652594 | ACATAGTTATCTGTT[C/T]ACTTGTTAGTATCTA | 10451 |
rs530147548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107659926 | TTAATGAATAAATCA[C/T]CAGAATACTACCAAA | 10451 |
rs530150163 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667601 | TAGGATTATTATACA[A/C]ACACACACACAAACA | 10451 |
rs530154871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736418 | AGAGGAAATCAAATT[A/G]TCCCTGTTTGCAGAT | 10451 |
rs530157921 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107748737 | TCAAACAGAAGATTA[C/G]AGCTCCCTCTTTCTT | 10451 |
rs530159560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921535 | CGGCCTGGACACAGT[A/T]AAGTTCTGGAAAGTG | 10451 |
rs530165373 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790868 | AATTTTTGTATTTTT[A/C]CTAGAGACGGGGTTT | 10451 |
rs530166066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824084 | AAGCAGGGAGACGTG[A/T]ACTGAGTAGAAAACT | 10451 |
rs530174184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107887104 | AAAGAGAACTTCTCC[A/G]TGGTTTGCTTCAACC | 10451 |
rs530179038 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107886509 | GGATGTCATTCCTCA[A/G]GAAAACATACTACAA | 10451 |
rs530193938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107741184 | ACAAAGTGAATCTTT[C/T]AAATTTTCACATTTG | 10451 |
rs530195023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755680 | AGCTGCATCACAGAG[A/G]CAATTTTAAAATGTC | 10451 |
rs530215142 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107749427 | AATGTTCAAGATTAT[A/C]AGTAAATTACAGTTA | 10451 |
rs530221954 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107713715 | ACCAATGTCTTCAAC[A/G]ACATCCTTATAAATA | 10451 |
rs530225184 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107698514 | TGCAGTTTTGACTTA[C/G]GATAGTTTCCACTTA | 10451 |
rs530235612 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701003 | CCATTCTGAATAGCG[G/T]GAGATGGTATCTTAT | 10451 |
rs530235974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719342 | CTAGAATCTACAAAG[A/G]ACTTAAACAAATTTA | 10451 |
rs530245716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707247 | ACAGATGTTAACTCT[A/G]TGACCCTGAAACTGC | 10451 |
rs530251979 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571562 | TCCATAACAAAGTTC[A/G]GCTGACGGCAACAGA | 10451 |
rs530258366 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107674403 | CAATTTCAGATTAAC[A/C/G]TTTTCAAAATTAACA | 10451 |
rs530278622 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107915259 | AAGAAAATAAGACTA[C/T]TAAAGGTTTAATGAG | 10451 |
rs530282839 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107943022 | CCTAGGCAGTGTAGA[A/G]TTCAGCTTCTCACAG | 10451 |
rs530295981 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107850541 | ACAGATGGGCACAGG[A/G]AGGGGAACATCACAC | 10451 |
rs530296068 | in-del | -/AC/ACAC | 0.00438571 | 0.0466605 | intron-variant | VAV3 | GRCh38.p7 | 1:107667597 | TGTTAGGATTATTAT[-/AC/ACAC]ACACACACACACACA | 10451 |
rs530305109 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943789 | TTTTACAGTTTGAAG[A/T]CGTGGCCTAGAGCCT | 10451 |
rs530307603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107706418 | TCTGCTGAATATGAG[C/T]GTGCTAAAAATGAAA | 10451 |
rs530313311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107616485 | CACTACCTATCAGGT[A/G]CTATGCTTAGAAACT | 10451 |
rs530313873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896831 | TATTAGAGGGGAAAT[A/G]TGAAACATTTGCCAG | 10451 |
rs530317183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886262 | TTTATACACATAACC[C/T]GATGAAGAAGATGCC | 10451 |
rs530322238 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107762410 | GTCAAAATGAATTGG[A/G]GACACATCCTGACAT | 10451 |
rs530339585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107803602 | AGTTTTATTTCATTG[C/T]GGTAAAAAAATACAT | 10451 |
rs530344663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667128 | TTTTAGCTCACCTTC[C/T]ATACCTCTGCTCCAG | 10451 |
rs530347543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936203 | TTAGTACTTGGAAAA[C/T]AAATCTGAAAATAAT | 10451 |
rs530359647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107844542 | TCAGATCCCCTGCCC[A/G]TGGAGCCCCATAAGC | 10451 |
rs530360002 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571925 | ATTTCAGAGATGATT[C/T]AAAATTTCAGAACTT | 10451 |
rs530368662 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586994 | AAGCCTGATGATGAC[G/T]TCTCAGGAGTGTTAC | 10451 |
rs530372356 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107578561 | TTAGAAGCCCTCATT[C/G]TAAACATTACTTCTG | 10451 |
rs530376327 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107803028 | TTGTTGCTCCTTATT[G/T]GTTTGCTGAAGTTTT | 10451 |
rs530385988 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908791 | TTTAAAATTTACATC[A/G]CCATCACCCAACACC | 10451 |
rs530390046 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649178 | CACAGGGAGTTCTTT[C/T]TACATAAGGTTATTA | 10451 |
rs530396851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107901514 | AACATGGTACAACAA[C/T]CAATGTAAAACAAAA | 10451 |
rs530404285 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107911364 | CAGACAAAGAAATTA[C/T]GAGTTCAACACAGGA | 10451 |
rs530406263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906583 | AGGCGGGAGAATGGC[A/G]TGAACCCAAGAGGCA | 10451 |
rs530413863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804872 | TTCTCTAAACTTTTG[C/T]CTGTCTGGCAAAGAT | 10451 |
rs530419852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107714667 | TACTAATTATGCTGC[C/T]GGTTATTTGAAAGGG | 10451 |
rs530430942 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720035 | GGACACAAGGCAGGG[A/G]ACATCACACACCAGG | 10451 |
rs530432961 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894330 | CTCAAAGAAGAAAAG[A/G]TAGAAGTAAAACAAG | 10451 |
rs530437840 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107580319 | GACTTCCAACAAAGG[A/C]CAGCAAAACACCAAG | 10451 |
rs530441547 | in-del | -/TCTC | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107913635 | AAGTACACAAAATAA[-/TCTC]TCTTTCTCAAAATCA | 10451 |
rs530443322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900062 | AAAATTATCTCTTCT[C/T]CTTCACTTTTCAAGG | 10451 |
rs530452199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913539 | AAAAGGAAGGAAATG[C/T]ATTGACCTTAAAAGT | 10451 |
rs530454357 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107622990 | AATAAAAGAAAAAAA[A/C]CAGCAAAGAGGAAGT | 10451 |
rs530458575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107577680 | AAAGCTACTATCTTG[A/G]TTCATGAGGAGGAAA | 10451 |
rs530470058 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774061 | CACAGACTTTTCTCT[A/G]TTTTTGCTGTTGTTG | 10451 |
rs530475453 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579481 | ACTAGCCTTGCAAAG[G/T]TAGTACACCGTTCAG | 10451 |
rs530491474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107810668 | GTTTTTCCCTCAGTG[C/T]TTGAGCTGAACAATC | 10451 |
rs530492768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726073 | TAATATTATGCTATC[A/G]ATATCCCTATCTCAG | 10451 |
rs530497742 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893793 | AGTTATAAGAAACTT[A/C]TTTTTTAAAGATCAA | 10451 |
rs530502769 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107768101 | AAGGTCTGAGGGTCT[C/G]GAAGAGCAACAGAGC | 10451 |
rs530509363 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929544 | CAGAATATTATATAA[C/T]ATTGTAACTATAGTA | 10451 |
rs530514264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107681962 | ACTGCACCCAGCCAC[A/G]TATGTTCTTACAAAC | 10451 |
rs530519055 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797417 | GAAAGATGTAATCCC[C/T]TTCCTTAGGGAGTTA | 10451 |
rs530519628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900433 | TTTTTAGGCCTTCAA[C/T]TCTTAACAGGGAGAA | 10451 |
rs530520440 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107907435 | AAAAATTTTAAGATA[G/T]ATGTATAACTGCTAT | 10451 |
rs530521727 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107816929 | TAGGCAAAAGCATCA[C/T]TGAACACGGCCAGAG | 10451 |
rs530526129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107809973 | TACTAGAAAATGATA[C/T]ATTGTAAAAACAACA | 10451 |
rs530528104 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689483 | GCATGGAACAGGAGG[C/T]TGGTTTGTTTTTTCT | 10451 |
rs530552622 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571800 | GGTCTTGAATCTATC[A/C]TAGATGAAAAGTCCT | 10451 |
rs530557868 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587750 | TGCGTGCCACCACAC[C/T]GGGCTAATTTTTTGT | 10451 |
rs530578596 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906689 | TAAAATACAATACAA[C/T]ACAATACATAAAATA | 10451 |
rs530580658 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107914065 | CTCCCAAAGTGCACA[A/G]ATTATTTTTAAGACT | 10451 |
rs530588763 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688811 | AACAAAGGTACTGCA[C/T]TGACGATTTGTAACA | 10451 |
rs530592720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777436 | CACCATGTCTAACAA[C/T]ATCTAGGGCTTTCCC | 10451 |
rs530593419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632088 | AACTAGTTTACAGTC[C/T]CACCAACAGTGTAAA | 10451 |
rs530593468 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107639887 | TACAGTGAGCTACGA[A/T]TGTAGTACCACACAC | 10451 |
rs530596267 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107798514 | ATGAGGTCAGGAGAT[C/T]GAGACCATTCTGGCT | 10451 |
rs530597632 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594989 | CTGGGGGAAATGTCA[A/T]AGCTTCAACAGAGTT | 10451 |
rs530598138 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107719632 | TAAACTACTTCAACC[A/G]TTGTGGAAGACAGTG | 10451 |
rs530598149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107952159 | ATCATGTCTTTTGCA[A/G]AGACATGGATAGCGC | 10451 |
rs530621365 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107821919 | AGTACAGGTGGCCTG[C/T]CTTTAAGTGTACTGC | 10451 |
rs530622611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107852293 | ATTTGAAGACTCAGG[C/T]ATGTTCCTAAAGGAC | 10451 |
rs530630127 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107747273 | CAGTCCAAGGAACCT[A/G]CCTGCTCTAGGACAT | 10451 |
rs530656207 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107824730 | GTAAAAGGTAGTATG[G/T]CTCAACTATAAACAT | 10451 |
rs530657772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107762926 | GAAAATAAAATGAGG[C/T]AGGATGAGCCAGGCT | 10451 |
rs530667115 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107646221 | TTGGAAACAGACAGT[C/T]ATATTCCTTAAAAAA | 10451 |
rs530668139 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764466 | CCTTCCTGTGGGCAA[A/T]ATGCATGGCCTTTTA | 10451 |
rs530674736 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107723955 | TTTGAGGTAGCTATT[A/G]TGTCTCCATTTTTTT | 10451 |
rs530677219 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654454 | GCATTATCCTATAAG[A/C]TTTTGTCATCTACAA | 10451 |
rs530681118 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107601373 | TTTAAAACACTGACA[A/C]CTGCCTTGAAGCAGT | 10451 |
rs530696195 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695237 | AAAGTTTGGACATTA[C/T]TCTGTAAGAAATGTA | 10451 |
rs530709140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731799 | ATGGAGGAGCTTTAA[C/T]CTCCTCTTCAGAGAA | 10451 |
rs530721773 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965680 | TGGTGTTTTGGCACC[C/T]TCAAAGTGAGTGAGA | 10451 |
rs530725268 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726066 | AAGATTTTAATATTA[C/T]GCTATCAATATCCCT | 10451 |
rs530732385 | in-del | -/A | 0.198634 | 0.244666 | intron-variant | VAV3 | GRCh38.p7 | 1:107837102 | AGAGAAACAATGGGC[-/A]AAAAAAAAACAAAAC | 10451 |
rs530732939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921323 | CTGCATCACATACTT[C/T]AGTGAAACACACTGC | 10451 |
rs530745798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776938 | AGATTCTATTTCTTT[A/T]AAATTGTTCCCTAAC | 10451 |
rs530752549 | in-del | -/AATC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107719366 | AAATTTACAAGAGAA[-/AATC]AAACAACTCCATCAA | 10451 |
rs530753420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107859109 | TTTGGTTTTTGGAGA[C/T]AGAGTCTTGTTGTGT | 10451 |
rs530764171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783845 | CGAGATCAGGAGATC[A/G]AGACCATCCTGGCCA | 10451 |
rs530770839 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702350 | CCCCTCCCTTGACAC[A/G]TGGGGATTACAATTC | 10451 |
rs530771473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731580 | ATTTAAACTCATTAT[A/G]AGGAAGAATCTTCTC | 10451 |
rs530790922 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107790820 | AGCCTCCTGAGTAAC[C/T]TGGATTACAGGCACC | 10451 |
rs530795080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886159 | CAAGATAATGCCTCA[C/T]GGCCATGACCCTGCC | 10451 |
rs530810037 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107719382 | ATCAAACAACTCCAT[C/G]AAAAAGTGGTCGAAG | 10451 |
rs530810282 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107823703 | CCAGTACCATTGTAT[C/T]TGGAGATGGGCTTTC | 10451 |
rs530820576 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107920526 | ATGATATCTCACAAA[C/T]GTGTATATCTCTGGA | 10451 |
rs530828387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872308 | CTTCAAAGGCTATAA[A/G]AACACTAGGTGCTGC | 10451 |
rs530828978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879609 | TTATCTGCTAGACCT[C/T]TGAATCATCTGAAGC | 10451 |
rs530830000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107609726 | AGGGCACTGGGCACT[C/G]GCATGCACACACACC | 10451 |
rs530831735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736034 | TGGCTTCATCCCTGG[G/T]ATGCAAGGCTGGTTC | 10451 |
rs530835462 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600925 | TTATCTTTGGCTCTG[C/T]AGCAGTTTTTTAAGT | 10451 |
rs530842508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831780 | ATAATAGACTCAATA[C/T]ACACTTAATAGCTTT | 10451 |
rs530847009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659843 | GGGTAATAAAATCTC[C/T]AATGAGAAACAAAAG | 10451 |
rs530854234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107748557 | CTATTAAAAATAAGA[C/T]ATATGCATTTACATA | 10451 |
rs530856037 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107653583 | AGTTTTCCTCCTTAA[A/C]CTTTTTCTGAAGTGA | 10451 |
rs530877812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831025 | CCACAAATACTTCTA[C/T]AGGTTGAGTATCCCT | 10451 |
rs530879623 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107640157 | ATGTCCATACAAAGA[A/C]TTATATTTGAATGTT | 10451 |
rs530879652 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107838761 | TGGGATACTGTGCAG[A/C]CCTAAAATAAAAAGA | 10451 |
rs530898637 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570963 | CAAGACTCACCGCAG[C/T]GGCCCTCCTACTAGA | 10451 |
rs530916847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107928041 | GCTTGTGTCACTCCA[C/T]CCCCAGCTCCAGGTG | 10451 |
rs530919994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107609273 | ATCTAGAAAATAATA[A/G]TTACTATCCATTACA | 10451 |
rs530924895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107623021 | GATCAGGAAAAGACC[A/G]AGTCAGAAACTAGCC | 10451 |
rs530927746 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107694156 | ACAGCCTAACCTTGG[A/C]AAATGCATAAAGCCT | 10451 |
rs530950771 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107892570 | TTTCTTTAACCAACA[G/T]TTCATCTTTGCTACC | 10451 |
rs530960426 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107697094 | AAACTCACACTCTAC[A/C]CACAGTTACCACCTA | 10451 |
rs530977454 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107740520 | GATAATTCATCCAGG[G/T]TTATAGTTTTTTTTG | 10451 |
rs530977651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107928729 | AGAAAAAAAAGAATA[A/G]ACAACAATGAAGCAT | 10451 |
rs530982236 | snp | A/T | 0.0310518 | 0.120672 | intron-variant | VAV3 | GRCh38.p7 | 1:107681344 | TTACTGATCCCTTGT[A/T]TAAACATTTTGTCTG | 10451 |
rs530997414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943727 | AGCCTGGCAACAGAG[C/T]GAGACTCCGTCTCAA | 10451 |
rs531002165 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702279 | TCATGAGAACTCACT[C/G]ACTATCATGAGAACA | 10451 |
rs531010388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107849768 | AAAAGAAACTATCAA[C/T]AGAGTGAACAGGCAA | 10451 |
rs531013068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747840 | GTCTTCAAAATATTA[A/G]ATAAAATAATCCTGA | 10451 |
rs531014582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891873 | AAAAAAAGAGCTCAG[C/G]GGTCAGACCAGGCTG | 10451 |
rs531018490 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790791 | CTCCCAGGTTAAAGC[A/G]ATTCTCCTGCCTCAG | 10451 |
rs531026301 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107860408 | AATAATTTAAGTTCT[C/T]GGGCTTTTAATTTAG | 10451 |
rs531034255 | snp | A/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589478 | AGGGGCATGGGAGGG[A/G]TTCTCCCTCAGAGCC | 10451 |
rs531035801 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107828121 | CTAAATAGTACACAG[A/C]GAGATTCATTCTGGC | 10451 |
rs531038597 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802468 | TTCAATATGCTATTG[A/C]CTATGGGTTTGTCAT | 10451 |
rs531062871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107578328 | TTTTATTTTTAAGTA[G/T]ACTGATACATGCCAT | 10451 |
rs531062889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107712856 | ACAAAGAAAGATCAC[A/G]TTAGGAAAACTTGAA | 10451 |
rs531070192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107857214 | CAGGATATAAAGCAG[A/G]CAGAAAAACACGAAA | 10451 |
rs531075738 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107890286 | AACATATGTAATTTT[A/C]TTAATAAATACCACT | 10451 |
rs531088786 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107622579 | CCTGGAATAGCACTG[A/T]ACAATTTGAAACAGA | 10451 |
rs531103137 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788232 | TTTCAAAACTATTAA[C/T]GTGATCATACCACCA | 10451 |
rs531105148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107899278 | ACAGTCATAGAGATA[C/T]ATTAATAAAAAAATG | 10451 |
rs531108120 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107905384 | ACATGTATTTGTTCT[C/T]TCTAGCTATGTGTCT | 10451 |
rs531123034 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107942318 | CAGCGAGAAGACAGC[A/G]GTTGCATTTCAACCT | 10451 |
rs531128402 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107950441 | GCTTGCTGGTACTAA[A/G]CGAGAGTTAGGGATT | 10451 |
rs531140303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107718376 | TCAGGATACAAAATC[A/G]AGGCGCAAAAATCAC | 10451 |
rs531143071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107898561 | ACCATAAAGATGACT[C/T]TTCCAAAATAAAGCT | 10451 |
rs531154741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107809100 | CTCCTTAAGAAGTAT[C/T]GTGAGATGCTCTTGT | 10451 |
rs531161302 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942955 | AGCAAACAAAACTCA[C/T]GTTTTCTTGTAGAGG | 10451 |
rs531169023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698267 | CTAGACTTTAATATT[C/T]GAATTTTGATATTTT | 10451 |
rs531184191 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107882770 | GTCCCAACAGAAGGG[A/G]CATCATCATCCTCAT | 10451 |
rs531186327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649315 | CCAGCGGCTGAAGAG[A/G]AGGCCAAGAGAGACA | 10451 |
rs531191537 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923374 | TAACCCTGAAGGTGA[A/T]GGTATTAGGAAATGA | 10451 |
rs531191874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780726 | TCGCTATGTCGGCCA[A/G]GCTGGTCTCGGACTC | 10451 |
rs531193068 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808585 | TTCATGATTCAAATA[A/C]CCATCAATGATCAGC | 10451 |
rs531197816 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815466 | ACCAAATTCAATGAT[A/G]TGATTTTACGCACTG | 10451 |
rs531198267 | snp | A/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594947 | GGAAGGCAAAGAAAC[A/G]GAGCTTCGAAAATTA | 10451 |
rs531201583 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107699859 | GCCAAGGAGGAGGGT[G/T]AGGTCAATGGATGGA | 10451 |
rs531202546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107957303 | CCTCTCTATCCCTCT[A/G]TTCACCTCCTTTCTC | 10451 |
rs531208702 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621441 | TTCTTTGGTTTCTTG[G/T]TGGATGTGTGTGGGA | 10451 |
rs531208970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107724268 | CCTCTACCACTCCAA[A/T]TGTGATCTATCCCTG | 10451 |
rs531218992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107680726 | CTACATATATTAGCT[C/T]ACGTAATGCTCACAA | 10451 |
rs531244166 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107644538 | TCAAATACTGGGGCC[A/G]GTTCTGAGCCGTGGA | 10451 |
rs531245335 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107657243 | TACAGGCATGAGCCA[A/C]CACGCCCGGCCTCTG | 10451 |
rs531259808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107663774 | AGCTACTTATGGATC[C/T]TAAATGAAACTCCTA | 10451 |
rs531262645 | snp | A/C/G | 8.26104e-05 | 0.00642644 | missense, synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107768450 | ACTCACAGGAATGTT[A/C/G]ATGAATACTGAATCA | 10451 |
rs531262811 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107868178 | TCCCATGGATGACAT[A/T]AAGCCCAAAGATTTC | 10451 |
rs531263187 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107604544 | TCAAGCTCCTTTTGC[A/G]CTTAGGGTCTTCTCA | 10451 |
rs531266686 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807176 | GATCATTTCAAATCA[C/G]GGTACTTCTCTAAGA | 10451 |
rs531270404 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107585533 | CCTTGAACCTCATCT[C/T]CAGCTACTCTTCCTC | 10451 |
rs531276293 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686920 | ACCATCTTCCTTGGA[A/T]AAAATAATATATATA | 10451 |
rs531282858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841824 | TTGGAAGAATAAGGA[A/G]AAAAAACAGAAAATA | 10451 |
rs531289058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744842 | TTTAGCACCCTTATG[G/T]ATAAAGAAACTCCTG | 10451 |
rs531315199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787747 | ATTTGATTAAAAGTG[A/G]ATATTTTTCAGATTC | 10451 |
rs531321106 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107605661 | TTCCACTAAAATGCA[C/G]ATTATAGTCAAAATG | 10451 |
rs531326737 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107751629 | ATATTCACAGAAGCA[C/T]GCAATTACAAACGCA | 10451 |
rs531331367 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107767651 | AAAGAACTGTTCAGG[C/T]AATACAAGCAGGTCT | 10451 |
rs531331637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953172 | GTCCTGTCTTCACCA[C/G]TTCCTGTCTGTGTGA | 10451 |
rs531344546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107882280 | AACCTGTGTGTTGAA[C/G]AAAGAAGCTCTCAGC | 10451 |
rs531358646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107703656 | CCGAAATGAGCTATT[C/G]TCTGTTTCACTCTTT | 10451 |
rs531378901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896031 | CTTGCAGGAAGTAAC[C/T]CTCCGTGCCAGAGGT | 10451 |
rs531385761 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107760221 | AGAACTAATGAGTCT[C/T]CTGGTATAGCTATCA | 10451 |
rs531399362 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946622 | ACATGGACAGTCATG[A/C]TATCCATAAAAGAGA | 10451 |
rs531402678 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940203 | CTGTAATGAAGAAAG[A/T]ATAGTTCCTTCAGAG | 10451 |
rs531407820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888777 | CCTGACTCACTTTGA[A/G]ACAAAATTATTCTCA | 10451 |
rs531420956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107834838 | ACAGCTCCTAAGGAA[G/T]AAGTGAGTGAAGTGA | 10451 |
rs531439278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933410 | ATTTCAAATTCTGAA[C/T]ATAAATGTCCTCAGA | 10451 |
rs531440798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107924199 | AAGTGACAGAAATTT[C/G]TCAACAACCCATTGC | 10451 |
rs531444023 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107847532 | CGCTAGCCACACTAA[C/T]AAAGATGAAAAGAGA | 10451 |
rs531444224 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107626419 | GTAATTAGGGACTCT[C/G]ATTTAACTCAGTATT | 10451 |
rs531447527 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612569 | CAAACAGGAAATCAC[A/C]GGGTTGATCTCCCTT | 10451 |
rs531465007 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107854110 | GGCCAGGGGTTCGAG[G/T]CCAGCCTGGCCAACA | 10451 |
rs531472423 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847440 | AGCAGAAATGAAGGA[C/G]ATAGAGATACAAAAA | 10451 |
rs531473898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107889479 | ATAATTGTGGTAAGA[C/T]AACAGGGCTTGATCC | 10451 |
rs531475387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107634259 | AAACAGCATGGTACT[A/G]GTACCAAAACAGTGA | 10451 |
rs531478625 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721460 | CTGAGAAAATGAGGT[A/T]TTCCCATGTTTAGAA | 10451 |
rs531497443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676957 | CAAGTTCCTCAAAGG[C/T]AGAGGAACTTCCACG | 10451 |
rs531497633 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107758217 | GTTAACTTTGATCCT[A/G]CCCCCTTGGAACCAT | 10451 |
rs531529233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716510 | GTGGTTTTTGTCTTT[A/G]GTTCTGTTTATGTGA | 10451 |
rs531544317 | snp | C/T | 1.65048e-05 | 0.00287265 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107765106 | GACATCTTCTTTTGT[C/T]TTAGAAATGTAGTCT | 10451 |
rs531549477 | snp | C/G | 1.64749e-05 | 0.00287005 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107574126 | TCTCCTTTCAACAAG[C/G]ACAACTCTCTCATAT | 10451 |
rs531566852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939725 | GTTTAGACAAAATCC[C/T]GAATGCAGGATTTAG | 10451 |
rs531568503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107799123 | TTCCTATGATAATTA[C/T]AGAACTTTGAAAGAG | 10451 |
rs531573729 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107878403 | TGCATTTGGCAGTTT[A/T]ATCTTTTAGTCAGTA | 10451 |
rs531576758 | in-del | -/A | 0.456214 | 0.141336 | intron-variant | VAV3 | GRCh38.p7 | 1:107891149 | AGTGTCCCTTTCTTT[-/A]AAAAAAAAAAAAAAT | 10451 |
rs531579921 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107727062 | AAGAGGATTTGATTA[C/T]ATCATTATTTTTGTA | 10451 |
rs531584208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107641521 | TCTTAACATAATACC[A/G]TATTTACCTAAGTTC | 10451 |
rs531585340 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918415 | GACAAGTCTTTAACT[C/G]TCTCAGAGTATTTAA | 10451 |
rs531585988 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107917223 | CTCAAGCATCAGCAG[C/T]GGCCTCACCAAAGTA | 10451 |
rs531589092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107582677 | GTTTGGTTTTTTGTT[C/T]TCGCGATAGTTTACT | 10451 |
rs531597083 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107812852 | GATAAGGCCGGGCAC[C/G]GTGGCTCACGCCTGT | 10451 |
rs531603977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107960784 | CTGTGTTCCTTCACT[C/T]GCTTCAGGTCCCACC | 10451 |
rs531618656 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107583284 | AGAGCTATCTGTGAC[A/C]AACCCACAGCCAAGA | 10451 |
rs531621071 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921385 | CTTCTCATATTGCAG[A/C]GGGTAAGGAACTGGG | 10451 |
rs531632565 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107765974 | TTGTCAGGAGATTTT[G/T]TTTTAACTTAGAAAG | 10451 |
rs531636716 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107846863 | TATTAGACAGATCAA[C/T]GAAACAGAAAATTAA | 10451 |
rs531637485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107909443 | TGAAAGATGAGTAGA[C/T]AATGGAAAAAAAAAT | 10451 |
rs531637540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107902286 | AAAGGCCATCTGTGA[C/T]TGAATGTACAATATC | 10451 |
rs531641854 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107683634 | AGCAAATGAATGTTG[C/T]ACATTTTCCAAGTCA | 10451 |
rs531648015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818964 | TTCAATTCAGTTTTA[C/T]GACACAAGAATTGCT | 10451 |
rs531649993 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107894804 | TTTCCCCCATAGAAG[C/T]ACCCCTAATGACAGA | 10451 |
rs531651607 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107611156 | TCTAAAATCGTATGT[A/G]CTCCAATGAGCATTT | 10451 |
rs531671386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903053 | TAGGAAGGGCTTGAA[A/G]TGTATCTCCAGCCTT | 10451 |
rs531672192 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107648060 | TACAACAGAAGCAGG[A/C]AATTTGGTGGAAAAC | 10451 |
rs531677558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107581803 | ATGAGCAGATGAAAA[C/T]TTACTCAGTTTTCAG | 10451 |
rs531677951 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107680772 | GGTCCTCTTATTCAT[C/T]TCCTTTTACAAATGA | 10451 |
rs531694484 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107943300 | TAGTCAGTTGAGGTT[A/G]GTCATATCACAGGTG | 10451 |
rs531695801 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923056 | GAGTGAACATTTCCA[C/T]CACCCTCAACAGCTT | 10451 |
rs531697178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107908634 | TTGGTGAGAACTAAA[C/T]TATGCATACTTTTCT | 10451 |
rs531698307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603559 | ATATATACTATGAAA[C/T]GAAATCTCCTTTAAG | 10451 |
rs531709182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690819 | TGCTATCCCTTCCTG[C/T]CCTCATGGCCACCAC | 10451 |
rs531716479 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107933322 | GATAACCTTTCTCCA[G/T]AAACTATTTGGTCCT | 10451 |
rs531734377 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655837 | ATTAGTCGTCAACAG[G/T]TATATGAAAAATTCT | 10451 |
rs531739368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953558 | TTAGTTGCTATTTAG[C/T]ATATTATTGCACATG | 10451 |
rs531743274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771468 | CCGTGTTAGCCAGGA[C/T]GGTCTTGATCTCCTG | 10451 |
rs531747966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107779257 | TATTCAACTCTATCA[A/G]TAAGTTCTACCTTGC | 10451 |
rs531763834 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107754140 | TTAGCTGGAGGGGTT[C/T]AGGAAAATAGCTTAA | 10451 |
rs531769478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702446 | AAGGGTAAGTAAATG[G/T]AGTTCAAAATCACCC | 10451 |
rs531775868 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726655 | GGCTTTGCAAGATAC[A/G]ATATGTTTTACTGAA | 10451 |
rs531776242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107602854 | AAATCTAATATGCCA[A/G]TTAGCAACCTATAAC | 10451 |
rs531777890 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107648557 | CCCTGGCAAACAGCT[A/C]TTCCCAGGGATGTAA | 10451 |
rs531786111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107867789 | GAAAATTCCAGACCC[C/T]TGAGGGAGGAAAAAT | 10451 |
rs531798829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107737706 | AAAGTCAGGAAACAA[C/T]AGGTGCTGGACAGGA | 10451 |
rs531807747 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966670 | GTCCTTTTTCGTTTG[G/T]CTGTGACAAGGATAG | 10451 |
rs531809515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818183 | CTGATCTGAATGCAG[C/T]GCTAATTCAGCAGAT | 10451 |
rs531813384 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632111 | AGTGTAAAAGTGTAA[A/C]ACCTTATTTTGTAGC | 10451 |
rs531816217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915016 | TTAGAGAGAGAGACA[A/G]CCTAAAGACAGGTAT | 10451 |
rs531825055 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690340 | ATGGTATTTACGGTG[G/T]TCAAGTAGCTACGGA | 10451 |
rs531826708 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107725146 | GAGAGGGGCATGTCG[C/G]TTTAGAGAGGTCACT | 10451 |
rs531829767 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107946554 | TAGAAATTTCGCATT[A/G]GAAAACAAAGCTGAA | 10451 |
rs531885273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107845995 | CCCCAAGACAAATAA[C/T]TATCAGATCCCCAAG | 10451 |
rs531890018 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786347 | ATATACTGGGCTGAT[A/T]AGAAGTGCAGGCTCA | 10451 |
rs531890056 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107777061 | AAACAGGAACTAAAA[A/G]CCAGTTGAAGTACAT | 10451 |
rs531890802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107930469 | TCAATTAGTCATTAC[C/T]AGAAATGACATACTC | 10451 |
rs531906671 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107839817 | AGATGACACAAATTG[C/T]TAATATCAGAAATAA | 10451 |
rs531927220 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107785717 | AGTGCTGGGTGGAGA[A/C]ATTCAGACAGAAGCA | 10451 |
rs531933244 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107697301 | AGGTCCTTACCATTT[C/T]ATACCGCTAATGAAC | 10451 |
rs531936602 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107861989 | TTTCTGACTGCTCTA[C/T]GCACTGGCCTGTCCT | 10451 |
rs531958482 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881652 | AAGGTGAGGAAGGAA[A/T]ATGGTAGAAAAGCAC | 10451 |
rs531972408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655342 | AGCCAAGTCATTTTT[G/T]ATAAAGGCGCCAAGA | 10451 |
rs531975210 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662170 | TTTTCAGCATTAAAT[A/C]CATTTTGCAAAATGA | 10451 |
rs531993532 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107732846 | CCCTGTCTGGCAGCT[C/G]TGAAGAGAGCAGTGG | 10451 |
rs531995924 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107661307 | TGCACGACCCATTAT[G/T]CACCCAAAGTGCTTG | 10451 |
rs532003118 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928073 | CTCAGAACAGAAAGA[C/G]AAACTCTATTTGGGA | 10451 |
rs532005008 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107793176 | TCATTTTAGAGACGG[C/T]TAAACTGAAAAAGAG | 10451 |
rs532006135 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107864870 | AGTGCCTTGAGAGCA[C/G]GGGGTCTTGACTACC | 10451 |
rs532008205 | in-del | -/ATTCCTG | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107795912 | GATATCCCCCATCCA[-/ATTCCTG]ATTCCCATACTGATC | 10451 |
rs532011657 | snp | A/T | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107897041 | CAGTCCACAATAAGG[A/T]TTAAACAGTACCCAG | 10451 |
rs532013990 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107742309 | ACAACAAAAATATGA[C/T]ACTGTGCTATGAAAG | 10451 |
rs532023318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750188 | TCACAAACAGGTCTA[A/C]TTTTGGAAACTGTGC | 10451 |
rs532037995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107669491 | ATAAAGACAAGAAAG[A/G]AATAAACACATTTTC | 10451 |
rs532048079 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662828 | AAGTTGGTAACCTTA[A/T]CCAACTCCAGCAGTT | 10451 |
rs532060361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107932648 | TCTCGAGATAGGGAG[G/T]TTATACTGGATTACC | 10451 |
rs532061218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107668368 | AAAGCTCAGTTTCAG[C/T]GTTTATTACTTACAT | 10451 |
rs532070103 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107726462 | CAGTCATGTCTCAGA[A/G]CCATCTTTGAGAAAG | 10451 |
rs532071174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895294 | AGGTGTAGAAAACCA[C/T]GGCTAACATTTGTAT | 10451 |
rs532079855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107846717 | ATAAATGCAACAAGA[A/G]CTAACTACCCTAAAT | 10451 |
rs532084860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107669595 | GTAGACTAGAGCCTC[C/T]TTTTCTTGCACAACA | 10451 |
rs532088797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676801 | TGTGTCCTTCAGTTT[C/G]CAAAAAATTCTCCCT | 10451 |
rs532089923 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107888827 | CTCTGTACTAAATTA[A/C]ATTCTATTTTCTGTC | 10451 |
rs532109925 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593493 | TCTGTATCCTCCAAG[A/G]ACTTTTAGAAGTAAT | 10451 |
rs532138990 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107740154 | TACCTGGGTGTGGTG[C/T]TGCGTGCCTATAATC | 10451 |
rs532144255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894486 | CATAATAAGGAAAGT[A/G]ATATAAATCTCATTA | 10451 |
rs532163976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625536 | CCTCCCAAAGTGTTG[A/G]GATTACAGGCATGAG | 10451 |
rs532170498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107861511 | AACTTTATAGATATA[A/G]GGAGCAGATGCATAG | 10451 |
rs532177782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619312 | CAAGGCAGAAAGAAA[C/T]GATCAGGAGAGAGAG | 10451 |
rs532186412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953496 | ATCATTTCTGCCTGA[C/T]CCCTGATCATGAAAC | 10451 |
rs532193550 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107749221 | ATTGTAGTCAACTTC[A/G]TATCTATAACAATTT | 10451 |
rs532204153 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805611 | AAAATTGCTATTTTG[A/T]ATTCTTGTTCAGAGA | 10451 |
rs532230379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107581703 | AAGTACTAGTGACTG[C/G]ATATTTGATGCCTAT | 10451 |
rs532236916 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107860836 | AGGACTTTGAGTCCA[G/T]CCTGGGCAACACAGT | 10451 |
rs532243066 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107852995 | AAATGAAGGCTTGTA[C/G]GTTTTTTTTTTAATT | 10451 |
rs532245101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107640737 | GCTTATGAATAGGAC[A/G]TGGAGTGGTAGAAAG | 10451 |
rs532245656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107931631 | TGGATATTAAAACAC[A/G]TGATTGAAATATTGT | 10451 |
rs532261828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107764512 | AATGTCATATTTTTA[A/G]TAAACATCTTTTTTA | 10451 |
rs532262620 | snp | G/T | 0.0437281 | 0.141251 | intron-variant | VAV3 | GRCh38.p7 | 1:107618643 | ATCCTTTATGGTAGG[G/T]CCAATTACTATCCCC | 10451 |
rs532263177 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107636568 | TAATTATATTAGCCC[A/G]CAGTTGGGCAAAATA | 10451 |
rs532265849 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840234 | GTAAATGTTACAGTG[C/T]TAGCAGTGTAAATCA | 10451 |
rs532268248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107708641 | GGACCTCTTTGTTCT[C/T]CAGATATGCATTCCT | 10451 |
rs532271350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107960314 | CTACTAAAATACAAA[A/G]AAGTAGCCGGGAGTA | 10451 |
rs532285994 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959145 | ACACACCTGTAATCC[C/T]AGCTACCTGGGAGGC | 10451 |
rs532290556 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107682891 | AACTGTGGAAAGAAG[G/T]CATTGCATAATGGAT | 10451 |
rs532299375 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107816531 | GATTCTGCAAAACTC[C/T]CAGCACTGTAAAATC | 10451 |
rs532300054 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107842158 | CCTTCATACTTATAT[C/T]GTCTACCTAGTACCT | 10451 |
rs532323305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721310 | TGCTACTGTATGGCT[G/T]TCTTAGTATTCCAGA | 10451 |
rs532328498 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107634190 | GCCAAAAGAACAAAG[C/G]TGGAGGCATCATGCT | 10451 |
rs532332793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814946 | CCTGAGCCTGATTTA[C/T]AAGCATCAATAGAAC | 10451 |
rs532336320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107770824 | CTGACTTTCTTAAAC[C/T]TTCCTTTCTAATACA | 10451 |
rs532342541 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107945356 | GGCATTTAACAAATA[C/T]CTAAAATTATTTCCC | 10451 |
rs532345046 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690295 | ATGTTCCATGAGGGT[G/T]CTCTGGGTGACCCCC | 10451 |
rs532353724 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107640033 | AATGTAACATGGTAT[A/G]GGCACTTTGAGTAAC | 10451 |
rs532355776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107647985 | TTTCATTGATCTGCT[C/G]GTCTTCAGAGAGGAG | 10451 |
rs532359525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107867120 | AAATACAATATGCAG[C/T]GTTTACCAAACTCAT | 10451 |
rs532364813 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966640 | AAAGAATGATCTGTT[C/G]AGGATAGTGATTGCG | 10451 |
rs532366632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107778311 | CATTTTATTATGCAA[A/G]TTCATTGTAGAAAAT | 10451 |
rs532371520 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107846139 | AAGAGAGTGGGGGCC[A/G]ATATTCAACATTCTT | 10451 |
rs532396813 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737206 | TACAAAAATCAATTT[A/C]AGATGGATTAAAAGC | 10451 |
rs532402140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107952896 | AAAGTAGAGGGGCTA[C/T]AAAATTACCAAAAAG | 10451 |
rs532406190 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107633077 | CTCAATTATAGTTCT[A/C]CTTTTAACATTATGT | 10451 |
rs532408363 | in-del | -/TCT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107701935 | TCCCACATCTTCCTG[-/TCT]TCTTCTGAGCCCTCC | 10451 |
rs532409730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589294 | TCAGTTAAGGATCTC[A/G]TAATGAGATCAAGCT | 10451 |
rs532417373 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107647296 | TTTAAAATCTAAACA[C/G]AGCCACATTAAAAAA | 10451 |
rs532419839 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681011 | TCATGTAGCATTTAT[G/T]AAGCACCTACTACCC | 10451 |
rs532432026 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107907917 | TTTAGAAAGATATGC[A/G]TTATACTAAATCAAG | 10451 |
rs532433338 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107736887 | AACAAAAAAGAGCCC[A/G]CATTGCCAAGACAAT | 10451 |
rs532437343 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107701234 | ATACCTAAACTTCAA[C/G]TCTTGACTTTTGTGC | 10451 |
rs532450924 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107817873 | GAGCGGAAAAAAATG[C/G/T]AATTTACTGCTCTGA | 10451 |
rs532468469 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107915991 | CATGTTGAGAGCAAT[G/T]AGGGGAGCATTTAAC | 10451 |
rs532469243 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107901935 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGGAG | 10451 |
rs532469738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107742281 | AAAACTTACAGAGTA[A/G]AATTTCAAATTTACA | 10451 |
rs532470550 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107602809 | AGAAATATACACACA[A/T]CAAACCACCAAAACA | 10451 |
rs532480640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107833098 | AAGCTTAGCGAGGAA[A/G]GCATGTCAAAAGCTG | 10451 |
rs532483206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107682225 | TCAAATATGTTCCTA[C/T]TGACATACTACAAAT | 10451 |
rs532485147 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107930375 | TTGATAAAAAACACA[C/T]TGAATATATATAAAG | 10451 |
rs532491486 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689590 | GGGCAGAAAGTCACC[G/T]TCAGAAGAAAAGCTA | 10451 |
rs532498701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588455 | CACTTCACACTGGGT[A/G]CCAGTATTGGAAGTG | 10451 |
rs532499900 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965865 | CTGCTTGAGAAAGGC[C/T]TGTGCCACGGTGCTA | 10451 |
rs532506719 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107610808 | CTTTAAAAATTCCTA[C/T]GAATAGGAGTACAGA | 10451 |
rs532507680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914953 | CTTTGAAAACTAAAG[A/G]GAAGAACTCATTTTT | 10451 |
rs532522541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107661272 | GCTCTGTGACATGTA[C/T]ACACAAGAGGTGCCA | 10451 |
rs532525617 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726251 | AACCTATAAAAAGAA[A/C]GAAAGAAATTGCTCA | 10451 |
rs532544512 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107880988 | TTAAACACATACTGA[A/G]GCTTAGAGATTTACC | 10451 |
rs532546801 | in-del | -/AAGTC | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693982 | AGAACCCATGTGTCA[-/AAGTC]AGCTGGCAAAGTCAC | 10451 |
rs532554917 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107771353 | TGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 10451 |
rs532566406 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107695882 | AAGGTAGAGTAAAAG[A/G]TTATCTACCTCTCAT | 10451 |
rs532576449 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107956255 | GAAAGAAGGGAGAAA[C/T]GGGTGATTAAGTTAA | 10451 |
rs532599193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107714464 | CCATAAGATACAATC[C/T]TAAAGCTCTCATTAA | 10451 |
rs532601821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107624832 | AGGCACTGTGTTACA[C/T]ACTAAGGAATTAAAA | 10451 |
rs532608077 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107741371 | GTGTGGGAGGCACTC[A/T]GTCCGGCCTGACTAG | 10451 |
rs532610902 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107766362 | GTAATAAACAGCAGT[-/A]AATAGCTATTTGTTA | 10451 |
rs532625931 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107884140 | GATGGGGCCCAGTTT[-/A]AAAAAAAAAAAAAAG | 10451 |
rs532627404 | in-del | -/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573011 | ATTCATGGTATCTGA[-/C]CAGAAGAAGTAAAGG | 10451 |
rs532628104 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833799 | TCACTTGGATGACAA[G/T]GGTGGCTTCAAAAAT | 10451 |
rs532637719 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107844733 | CTCAGCAAAGCCCCT[A/G]TAACCACACTTCCTC | 10451 |
rs532641707 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107944480 | AAAATATACCTCTCT[C/T]ATAACCTGAATTCTT | 10451 |
rs532657248 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107804280 | TACTGGTGTCATTTT[A/G]TTGCTTGTTTTCTGG | 10451 |
rs532658404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107838955 | ACTACTAGAGCAAGG[A/G]GAGGAGAGAGGCAAG | 10451 |
rs532666918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936493 | TATGACAATCTAGAG[A/G]AACAACAGTGACAGT | 10451 |
rs532669450 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107901650 | AAAATAAAAATAAAA[A/G]TATTTTTCCTTTCAA | 10451 |
rs532671110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756518 | TAACACGAATTGGTA[C/T]AAGGACACAGTTAAG | 10451 |
rs532673530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107845385 | CAAAAACCAGAATGC[C/T]TCTCATCCTCCAAAG | 10451 |
rs532676365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107922557 | TAGTAATTTCCTAAC[C/T]ATCATCAACTTAATT | 10451 |
rs532685916 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107623898 | CTTGTAAAGTGGCTG[G/T]CATTGGCTTAGAATT | 10451 |
rs532687105 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571633 | GGAAAGAATCCATTC[C/T]AAGAGTACACTTTGA | 10451 |
rs532716249 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107795295 | TAACTTAGTAAACTA[C/T]GTCCTTTAAACCCTT | 10451 |
rs532727945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579390 | GTCTGAAACCAAATT[C/T]CTCAACTTATTCCCT | 10451 |
rs532735758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107609862 | GGTTTACTACCCCCA[C/T]ATTTAAGGCATCCTG | 10451 |
rs532737568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107791422 | AATAGTTCAGGTGAT[A/G]GAGTACACATGTGAA | 10451 |
rs532751516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107788054 | CATCCTTTTCAGACT[C/T]TCTCAGATCCAATCC | 10451 |
rs532756537 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107655174 | AAGCCAAAGCAATCC[C/T]GGACAAATGGAATAA | 10451 |
rs532758410 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963683 | GCGTCATAGAGGATT[A/C]GTGCTGAAATGTGTC | 10451 |
rs532775722 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107600118 | GGTTCTTGGTGTAGA[C/T]GTATTTACTGATTCT | 10451 |
rs532777308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790920 | CTCAAACTCCTGACC[C/T]CATGATCTGCCCGCC | 10451 |
rs532795705 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107956749 | GCCCACTTGAGGTTA[C/G]GGATCATGAACTTAA | 10451 |
rs532796351 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107597143 | AAATTTCTTATAAAT[A/G]TCTGAAATGAAAATA | 10451 |
rs532799981 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774033 | CAGTAAAGGAATGAA[A/T]CATATAAATTAGCAC | 10451 |
rs532805254 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107713887 | TCCTATAAAGTCAGA[C/T]ATCACGTTTTGGCTA | 10451 |
rs532805438 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107932857 | AGCAAGAAAATTAAT[C/T]TCCTCCTTGAAGCCT | 10451 |
rs532806085 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700319 | ATTTTATTTTAAGTT[C/G]CAGGGTACATGTGCA | 10451 |
rs532812562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107643799 | TCCTCAAAATTCTTT[G/T]GAACAACATGCCAGA | 10451 |
rs532816473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107748861 | ATTCCCGTCGCTGTA[A/C]ACATTATACATGCTA | 10451 |
rs532819252 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957488 | AACAGGCAGACTGAG[G/T]CTGTCAGTATGAATT | 10451 |
rs532831844 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928891 | AAGATATCGATATCC[A/C]AGTATAATAAGGTTC | 10451 |
rs532835780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729425 | GAAAAATGCAGAAAG[C/T]CTATAGTTTGGGGTT | 10451 |
rs532849842 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107892839 | TTTTCTTGGCCTAGA[A/T]TTCCCCCATCCCTAT | 10451 |
rs532853220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107937112 | CAAAAAAACAGCTCC[A/G]TCATTCACACCATAA | 10451 |
rs532855701 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107667668 | TATTTAAAATAGCAA[C/T]ATCCTGCTTAAAACC | 10451 |
rs532857496 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107626040 | AAAAGAGATAATACT[G/T]CATTGTCTGAACTTC | 10451 |
rs532862792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821273 | GTTGATTGTTCAGAA[C/G]TATGATAGACATTAA | 10451 |
rs532866238 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107644213 | ATTTTACATATTCTA[C/T]TAAGTTGCTACTGCT | 10451 |
rs532866473 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107674543 | ACCACAGGAAATAAG[C/T]TTTTCTCTGTCCAAA | 10451 |
rs532870032 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571208 | TTTACAAAATAATAC[A/G]AAGTGAAATACCACT | 10451 |
rs532879531 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107618273 | TCACCTTTATATTCA[C/T]TGGCATAAGCAGATC | 10451 |
rs532879592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107836985 | ATGTACAAAGAAAAA[C/T]TGGTACCAGTCCTGC | 10451 |
rs532883377 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593950 | CATGTAAGAGCACTA[C/T]GCTAAGTGCTTTATA | 10451 |
rs532889289 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107678650 | TTGGAATAAATTTCA[C/G]AATCCTTTGAAATTA | 10451 |
rs532895954 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963034 | ACATCTAACATAAGA[A/G]GAGAAGAGTGAAACA | 10451 |
rs532900240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107828718 | TTTTCAGGACCCATA[C/T]GATTACATTGGGCCC | 10451 |
rs532912274 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107693977 | AACCCTAGAACCCAT[A/G]TGTCAAGCTGGCAAA | 10451 |
rs532924635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686311 | CCTCGCAAATAAAGT[A/G]CAAAATTTAAAAAAA | 10451 |
rs532935438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592339 | TTTGTCCTGCTTGGA[A/G]CATTATATTAGGAGG | 10451 |
rs532953360 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107614567 | TAGTCTTGCTTACAA[G/T]TATAAGTTACTCTAC | 10451 |
rs532974904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107606645 | TGCTAAACTTTATTT[C/T]CCAAGTCTTCTATAA | 10451 |
rs532986205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821862 | AAGAGCAAGGTCTCG[C/T]ATAAAGAAAGTGATT | 10451 |
rs532987905 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107700498 | TGTTGTTCCCCTCCC[A/T]GTGTCCATGTGTTCT | 10451 |
rs532988029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613906 | CTGTCACCCAGACTG[C/G]AGTGCAGTGGAATAA | 10451 |
rs532989792 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107954331 | ACCATGTGCTTGAGA[-/C]CAGCTGTCACAAGGC | 10451 |
rs532995015 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814413 | TAGTGATGTTGAGTA[C/T]TTTTTCATGTTCCTG | 10451 |
rs532998848 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107877278 | TGTATTCTACCAAGA[C/T]AGATAATAATTACTC | 10451 |
rs533009941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599711 | GGCCAATCTTCTCAC[G/T]GAGAAACCAGTTAAT | 10451 |
rs533011171 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107946217 | TGAAAGATGGAGAGT[A/G]GAGAGGAGCAGACAT | 10451 |
rs533015855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657901 | GTCATGGAAGAGAAA[C/T]TGCTAACTAATTGCT | 10451 |
rs533025327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107829415 | CATGCTCTACATTAA[A/C]GTGTATTAGAATTAA | 10451 |
rs533028591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107941364 | GCAACAGCATCTGTT[C/G]CAACGGCTTTTTGCT | 10451 |
rs533030346 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107740630 | AAAAAATCACACTTC[C/T]ACAAAAGGCCACAGC | 10451 |
rs533046619 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107706339 | TATGAAAAAACATTC[A/G]CAAAGGCAATTGGAG | 10451 |
rs533047786 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107926761 | TTAAACCAGCCCTGG[A/C]CAGAGGGGAATTTTC | 10451 |
rs533056222 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107745836 | GCTCCCTTGATTTCC[A/C]TCCACCCTCTCACCA | 10451 |
rs533058350 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107906569 | TACTCGGGAGGCTGA[A/G]GCGGGAGAATGGCGT | 10451 |
rs533075818 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620941 | GTTGTATAAGAAATG[C/T]TCTAAAACTAGATGA | 10451 |
rs533083416 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107911049 | TCTCTCTCTATTCAA[C/T]ACCACCAGACAAATA | 10451 |
rs533089687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710308 | ACATAAAATGGTTTA[C/T]TTCATCATATTGCAT | 10451 |
rs533092752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699411 | GCTCTGCCCCTATGG[C/T]GTTGCAGGGTACAGC | 10451 |
rs533093257 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107752192 | AATAAGTCCTCACAT[A/G]TATGGTCAAATGATT | 10451 |
rs533094387 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107877981 | CAGCCTGCCAGCAGT[A/C]CACTCCAGGACTTTT | 10451 |
rs533107894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107704777 | TTGGTAGAGGGAGAC[A/G]AGCTTGCCAGAGCTT | 10451 |
rs533110379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107789155 | TTCCATATGACCTAA[A/G]GGACTTAGAAAGTTT | 10451 |
rs533141527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107883562 | GTAGCAATGTGTCTT[C/T]TTAAACTTACCTAAG | 10451 |
rs533144421 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107897071 | GATGGCAACACAAGG[A/T]GCCGGAGCAGCACTG | 10451 |
rs533153399 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717232 | TTTTGTGTGTCTCTA[C/T]TTCCTTTAGTTCTGC | 10451 |
rs533168634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107884398 | CCCCAAAATTAAAAA[C/T]AAATTATTTATTATT | 10451 |
rs533172699 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107855699 | GTTAGGACTGGTAGG[A/G]TGACCCACAATAAAT | 10451 |
rs533181979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807226 | TTCTAACCCTTTCCT[C/T]GTGTTCCTTTGTCAA | 10451 |
rs533187768 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948406 | AAAACCTGCATTTAG[A/T]CTGGTTCTGGCAAAC | 10451 |
rs533189446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940567 | CTAAAGCTTAAAACT[C/T]GATTGGGAGACAAGT | 10451 |
rs533215645 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107583655 | GAACTCCCATTCACA[A/C]TTGCTTCAAAGAGAA | 10451 |
rs533215815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591267 | TTCAGCTTCATAAGG[A/G]TTATCAAAATTTGTG | 10451 |
rs533220011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107813628 | TTTCAAGTCCTCTCT[C/T]CTAGCTATTTTGAAA | 10451 |
rs533224179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933612 | GAGCCCAGGAGTTAA[A/G]AGACCAGCCTGGGGA | 10451 |
rs533227483 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107722178 | GAACACAGCCTCATT[A/C]TCCACTGTGATGTAT | 10451 |
rs533232961 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107899131 | ATGGTTGTCCTACCT[A/G]CAAGGGTGGGGGCAG | 10451 |
rs533235836 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107753177 | AGGATGAACTTTGAA[A/G]ACATTATGCTAAGTA | 10451 |
rs533236466 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107954999 | TAGATGAGATAATGC[A/G]TGGAAAGCTTTAGTA | 10451 |
rs533238907 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107634916 | AAATCAAAACCACAA[C/T]GAGATACCATCTCAC | 10451 |
rs533242439 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107585774 | CAGAGAAGTAGGTAG[C/T]GTGCATGCAATCTCC | 10451 |
rs533246543 | in-del | -/TG | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107923181 | TGCCTTTTCTAAAAC[-/TG]TATATAAATGGACTC | 10451 |
rs533250428 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677814 | TCTCCAGATATTCAC[C/G]TCACCTTTGTTCTGA | 10451 |
rs533278935 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107760444 | TCTGCCAAAATTCAA[A/G]TGCACTGCAATATTG | 10451 |
rs533278984 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107882432 | AAGGCACAGAAGAGA[C/T]GACCATGAAACCGAT | 10451 |
rs533292022 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107575838 | AACAGACTTTATCTA[A/T]TGTATACCCTAAATG | 10451 |
rs533297766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903969 | TCCCATGCCCTCATC[A/G]ATCTGCAGCTGGATA | 10451 |
rs533300369 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107910985 | CAAGACTCAGTCTCA[C/T]TAAAAGAAAAAAAAA | 10451 |
rs533305288 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107691969 | TATTTTGTTTTTCAA[C/T]ACAAGTGGCTCTCAA | 10451 |
rs533307092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107909576 | CATACCCATCACATA[C/T]AGCATAGAATTGACA | 10451 |
rs533316001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107759693 | AGGGGGAACAGTTTA[C/T]TAAATTTCAAAAAAG | 10451 |
rs533328644 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107831153 | GATAGCAAAAATTTT[C/T]GGGTTTTGTGAGTTT | 10451 |
rs533348492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107728268 | AAGGTACTCACTAAC[A/G]CAAGATCTGTTCTAA | 10451 |
rs533368591 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897645 | CATTCACCCTGCCCA[G/T]GACACCACGGTAACT | 10451 |
rs533372490 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107722881 | TAAGTAGTTCTAATC[A/T]TTGCATTCATAGTGA | 10451 |
rs533372855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635492 | GGGGGAGGGGGGAGG[A/G]ATAGCATTAGGAAAT | 10451 |
rs533402436 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580313 | CCATAAGACTTCCAA[A/C]AAAGGCCAGCAAAAC | 10451 |
rs533419258 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107587046 | ATTAGGGCTAATGGG[G/T]ATGGTAAGTTTGAAG | 10451 |
rs533436663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107826936 | TGTTTCAGTTTTTTA[C/T]ATTAAAAAGATAATA | 10451 |
rs533444709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107924131 | AGAAGGGACATGGCC[A/G]TGGATACAACCTCTT | 10451 |
rs533452514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107766828 | GATAAGGGGAAGGCA[A/G]AGGAGAGGGAGGAGA | 10451 |
rs533458156 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759042 | AGCTTCCCTATACAT[A/G]ATTATTTAGGCCTTT | 10451 |
rs533462205 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903171 | GGATATTTAATTTTT[A/T]AAAAAAATCTGAGCA | 10451 |
rs533465245 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107604299 | AAACGCACATGACAG[C/G]CATTCAGCAAAAGTT | 10451 |
rs533465500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107916582 | TACAATTTGTACAGG[A/G]AAAAAATTTTACAGG | 10451 |
rs533470257 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107820330 | TGGATAGAACTGGAG[A/G]ACATTATGCTAAGTG | 10451 |
rs533475382 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107656724 | CAAAAGTATGCACAT[C/G]TATTATATATCAATA | 10451 |
rs533476416 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582783 | TTCCATGGTGAATAT[C/T]TGCCACATTTTCTTA | 10451 |
rs533483543 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107849394 | ATATATTGACCAATG[C/G]AACAGAATAGAGGCC | 10451 |
rs533493426 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107766202 | TAGCCTTTTGATTTG[C/T]GATGCAAAAAAATAA | 10451 |
rs533494847 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107773492 | CCCATTCAGAGGAAA[A/C]CCACCAGTCCCCCAT | 10451 |
rs533502694 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107784782 | CAAATAAAAGAGTAA[C/T]ACCTTGCTAAATTGT | 10451 |
rs533520094 | in-del | -/TCT | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107935143 | CATAAATTCCTAAGG[-/TCT]TCTCCATTTGGGGGC | 10451 |
rs533520153 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107837558 | AATTCATATGGAACC[-/A]AAAAAGAGCCCAAAT | 10451 |
rs533528550 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107805363 | TTCCATTCTTTCTTT[A/T]TTCTCCTCTGTGTAA | 10451 |
rs533533984 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781275 | GCTTAACTCAGTAAA[G/T]GTGAATTTTTATTAT | 10451 |
rs533539651 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107583255 | GCCCACTTTTTGATG[G/T]GGTTGTTTGAGTAAG | 10451 |
rs533548521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107773035 | ACAGAATCCAATAAC[A/G]AGGGCAGTGGCAGCC | 10451 |
rs533550046 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107642252 | AGGTTGCAGTAAAGA[A/G]GCCGGCTAAATCCTA | 10451 |
rs533557348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597801 | AACCATTTCACAGAT[A/G]ATAACAAAGAATATA | 10451 |
rs533561463 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107692731 | GGAGTGGCTATAGCA[A/G]CAGCAGGAGCAGCAG | 10451 |
rs533566067 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107961016 | ACTAAAATCCAAACC[C/G]CTTTAGGGCAGGGAC | 10451 |
rs533571199 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107729358 | GTATATGATAATAGA[C/T]GAGAGAATTGTGTTT | 10451 |
rs533573272 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107855276 | GTATTTAACTCTATT[G/T]ATTTTATTTTATTTT | 10451 |
rs533578304 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107954224 | ATTTATAATAGAAAA[A/C]AAATGCCCTATCAAA | 10451 |
rs533594731 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107903401 | TTCCTAGGCATCCCC[A/C]AATGTGACCTCTGAG | 10451 |
rs533598183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649414 | TAAGTCAGCAAAGAA[C/T]AATTTCTGACTTCTG | 10451 |
rs533609261 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107641889 | TAGTATTTTTCTCTA[G/T]TGTTCCAATTTTTGT | 10451 |
rs533610286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649256 | CAGGGCTGGTGATTA[A/C]CTTAACTCAAAGACT | 10451 |
rs533623479 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107955344 | ATTTGTAGATGTTTG[-/A]AAAGGTAGTAAAGAG | 10451 |
rs533624402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107648818 | CAGGTTGGTCATTCT[A/G]TGCAACCTACAGGGA | 10451 |
rs533630713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738147 | ACTCATAGGTGGGAA[C/T]TGAACAATGAGAACA | 10451 |
rs533670448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737797 | TGGAAGACAGTGTGG[C/T]GATTCCTCAATGATC | 10451 |
rs533675675 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107817385 | TGGGTAACAGGGAAT[C/T]ATCAACCACAGCAAG | 10451 |
rs533679574 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107691361 | CCCATTTTTACTTCC[G/T]TTTGGTATCCACCTG | 10451 |
rs533680751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744754 | TCCTATTCACAGTGA[A/G]AAAACAAAAACAAAA | 10451 |
rs533685110 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107834781 | GGAAGCTGGGAACTC[C/T]GCATGGGGTTGCTGA | 10451 |
rs533690222 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107869375 | TGCACTTAATTCAAA[A/G]TTCGACACCTATGTT | 10451 |
rs533695007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107826297 | ACTTGCTATGCAGAT[C/T]TGAAACCTGTAAGAT | 10451 |
rs533719675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906978 | AGCATGGGTGGAGGT[C/G]CAAGTATCTTATATG | 10451 |
rs533724762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107780034 | TGGACAGTCCTGCTA[C/T]ATAGCAAAGCAGGTG | 10451 |
rs533742087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107684793 | AGCCAAGGCACAAAA[A/C]TTGGAAGCATAATGA | 10451 |
rs533749102 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107876020 | GAGCAAAGAAGAGGA[A/G]AGTACCTGAGCCAGG | 10451 |
rs533751879 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590985 | TGTAAAACTTCAATA[C/G/T]TTTCCTAGTGCAAAT | 10451 |
rs533762657 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107635106 | ACCATTTGACCCAGC[A/G]ATCCCATTACTGGGT | 10451 |
rs533766112 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107871337 | CCCCCATTCCCCCCC[-/T]CTCCCCCCACCAGAC | 10451 |
rs533775922 | snp | G/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594324 | AACCAGAACAGTGCC[G/T]TGTATGTGTTAGGTG | 10451 |
rs533778538 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950653 | AGGGCAGCAAAGCCT[C/G]AGAAGGAGGGTGCTC | 10451 |
rs533784936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737998 | AAGAGAATGTGGCAC[A/G]TATTCACCATGGAAT | 10451 |
rs533788260 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107738837 | GACTTAGTACAACAA[-/AC]AACTCCAAAACAATC | 10451 |
rs533792556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107947030 | CCCAGAGGGAAAAGA[A/G]CCTGCCCTAGATCAT | 10451 |
rs533793608 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107663670 | GTAGTATTTTACCTC[C/T]GCTGAAAAATCTGAT | 10451 |
rs533795154 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580674 | GGGTCCTTAATTCCT[G/T]TGAGCTGGAAAAACA | 10451 |
rs533798365 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107692082 | CTATCTCAACAGGGG[A/C]CACAGAAAAGTAATT | 10451 |
rs533802470 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107863252 | TTCTTAAACATCCCA[A/G]ATCTCTCAAACTCTG | 10451 |
rs533803777 | in-del | -/TTTGCTTTCTC | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107882009 | TTTCTCAAAGATATG[-/TTTGCTTTCTC]AATGCAAACAGGATG | 10451 |
rs533814749 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107841359 | ATAAGAAATATGGGG[A/G]AAAAAACTAAAGCAA | 10451 |
rs533825314 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959535 | TTTGACATGTCATCG[C/T]TCCTCCCAAAAATAC | 10451 |
rs533827723 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107642467 | CTCGGGGCTGCTCTG[C/T]CTATGGAGTAGCCAT | 10451 |
rs533831074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656212 | AACCTAAGTGTCCAT[C/G]AATGGATGGGTGGAT | 10451 |
rs533840865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888480 | TTGTGTTGTTGGAGA[C/T]GGACTTTCTCTCTTG | 10451 |
rs533848662 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107743865 | ACTTGGAAACACTGT[C/T]CTATTTGACCTCGGA | 10451 |
rs533855116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619518 | ACACACTACAATGCT[A/C]CCTGAGTGCAAAATA | 10451 |
rs533856380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819903 | AAAATCAAAACTACA[A/G]TGAAATATCATCTCT | 10451 |
rs533856821 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107921613 | GTCATCACTCCATAA[C/G]CAGCCATCCCTTAGA | 10451 |
rs533856879 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107639491 | AATAAAAAAATGCAT[A/G]GCTCATTAAAAAGCT | 10451 |
rs533861828 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107611938 | ATGGGTCCTTGTCTG[A/G]CAAGTACTTCATATT | 10451 |
rs533886598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750713 | TACATCTGCAAATTT[C/T]CCTCAAGAAAATATT | 10451 |
rs533891649 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618894 | TCATTGGTGATGGCA[C/T]TTCTTTAAAGGTGTT | 10451 |
rs533907174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107827165 | CATTCAGTCAAGGGT[A/C]CTCTGAGCTAAATAA | 10451 |
rs533912813 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107669840 | AATAAAAAACTCCTT[A/G]GAGGAGAGAGTAACT | 10451 |
rs533913055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738293 | AACCAACATGGCACA[G/T]GTATACATACGTAAC | 10451 |
rs533920958 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107708894 | GCTTAAAAATACCTC[C/T]TCAAAAACTCAGGTT | 10451 |
rs533929339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780773 | CACCTGCCTTGGCCT[C/T]CCAAAGTGCTGGGAT | 10451 |
rs533940636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786585 | GCTGCTATTTCTAAC[A/G]TCATCATCACCTTTG | 10451 |
rs533943517 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621220 | CCTAGCAGTTCAGGT[C/T]CCATTTCTTAAATGG | 10451 |
rs533944552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107835166 | GCATGCTCCCCTGTC[C/T]ACCAGCCGCTATCAA | 10451 |
rs533946008 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726757 | AATTGATTAAATAGA[G/T]TTTGATTATTTTAGC | 10451 |
rs533960297 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107731902 | AAAAAACAACTATGA[A/C]AAATCAGTTTTTCTA | 10451 |
rs533961479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107882321 | AAAGAAGTTCTCAGT[A/G]GGACACTTGCTATTG | 10451 |
rs533974590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939296 | AATTCTAGACTCAAA[C/T]TTTCTTGCCTTTACA | 10451 |
rs533976936 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107625847 | TCAAATCAATAATCA[C/T]GTCAGATGGAATTCC | 10451 |
rs533977907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107715460 | TGAGATAATGCTTTT[A/C]TTGTATTAAACATGT | 10451 |
rs533980456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107932842 | CTGGAAGTTGAAGAA[A/G]GCAAGAAAATTAATT | 10451 |
rs533981752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107703104 | TCTTCACAGATATCA[C/T]CTCATCAAGACAGGG | 10451 |
rs533987938 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107853633 | AATGTCTTTAAAAAA[A/T]AAAGTTATTTTTGAT | 10451 |
rs533999074 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107709620 | AGTTCCAATAATCCC[C/T]ACGTGTCGTGAGAGG | 10451 |
rs534006390 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107626838 | ATCAGTTTTCTTAAC[A/G]AAGGAGATCTGATTC | 10451 |
rs534024208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612652 | GAGTAATTTTATATT[A/G]TATCTTGGACAATTT | 10451 |
rs534039496 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107916013 | GCATTTAACTCAGCG[G/T]AGAAGTTCAGAGAAG | 10451 |
rs534043116 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107726754 | TGAAATTGATTAAAT[A/C]GATTTTGATTATTTT | 10451 |
rs534049088 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107702752 | ATCCACGTGTACTCC[A/G]GATCATGAAAACAAT | 10451 |
rs534055914 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107916478 | TGACCCTCTAAAGTT[A/G]ACTAATATTTGAGTT | 10451 |
rs534062907 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709361 | TTGTTTGTTTTCAAA[A/C]GCTGCCTTTTGCCAC | 10451 |
rs534063948 | in-del | -/ACAA | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107727565 | ATTTAAAAACCAATT[-/ACAA]ACAGTCTACTAATGA | 10451 |
rs534089972 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923826 | GGGGACACAAAGCCT[A/G]ACCATATCAAGGCCC | 10451 |
rs534091398 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107663074 | ATGCGGTAAATCCAC[A/T]TTCTTGTATAAACCA | 10451 |
rs534111353 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107633200 | ATGAAAAAAGATACT[A/T]TACATAATTAAGTTT | 10451 |
rs534112081 | in-del | -/ACACT | 0.0345262 | 0.126772 | intron-variant | VAV3 | GRCh38.p7 | 1:107753561 | TATACACACACACAC[-/ACACT]TTTTTTTTTTGAGAC | 10451 |
rs534113323 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588752 | GGCTAGAGATTCCTG[C/G]AATACTCCATTGGAG | 10451 |
rs534117432 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107867866 | TAAGGGCTGAATGAG[A/G]AGGATGTGACCCAGG | 10451 |
rs534119204 | in-del | -/TATTTTA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107705629 | AATAATTTTACCATT[-/TATTTTA]TATTTTATTTATATT | 10451 |
rs534119439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959952 | ATTCTGGAGACATAC[C/T]TGACTCCTCTCTTCT | 10451 |
rs534149292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726370 | AAGTCCTCTGTGCTC[C/T]GGCAGAGGCGCTCTG | 10451 |
rs534149748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107758336 | GCACATTTCCAGGCT[C/G]AGATGGGAGGATCAC | 10451 |
rs534167350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818357 | TTAGTGGAAATGCAC[C/T]CAGTGCAGTTTTTTT | 10451 |
rs534171608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107640363 | TGAAATAAGCCATAC[A/G]AAAAACAATATATGC | 10451 |
rs534173160 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107716307 | ACATTATTGTGACCA[A/G]ACAGCCAGCCAGTAA | 10451 |
rs534175401 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107747225 | TTTGTTTTATGGCAA[A/C]TGAACAAAATAGTAA | 10451 |
rs534181614 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952645 | CACCTACCAAACTTT[A/G]GCCATGCCCATTCAC | 10451 |
rs534182516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107799184 | TTTCACTTTTTAGTT[A/G]CCTCATTTCATATTT | 10451 |
rs534186974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107922680 | CAATTTGGCCGGGCG[C/T]GGTGGCTCACGCCTG | 10451 |
rs534200323 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107654481 | ACAATTTTTCAATGT[A/G]AAATATTTGAAATGT | 10451 |
rs534202582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825658 | TTTCCTACCCCAATG[C/T]CTCTGCCCAAATAAA | 10451 |
rs534204191 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107780018 | TCACAGAAAGTTCTA[C/T]TGGACAGTCCTGCTA | 10451 |
rs534204577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107817444 | AACTGGACAAGCTGG[C/T]TAGAGTCAGATTATA | 10451 |
rs534210241 | snp | G/T | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964154 | CCTGTTCTTCCCTTT[G/T]ACCAATGTCACTCCT | 10451 |
rs534215987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107732256 | CCGTTTCAAGATGAC[C/T]GAATAGGAACAGCTC | 10451 |
rs534224412 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889644 | AAATAAAACCCTACA[C/G]CACATCTGCCTTACA | 10451 |
rs534229073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595501 | TTATTTAAAAAAAAT[A/G]AAGTGATATCAGATT | 10451 |
rs534230204 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107840896 | AAAACTCTGAGCAAG[A/G]GATCAACATGTTCAG | 10451 |
rs534234315 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805795 | GGGTATGTTTGCTTA[C/T]AGATTCTTTGTAATT | 10451 |
rs534239840 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107838653 | AGAGACACATGCATC[C/T]GTACATTCATTGCAG | 10451 |
rs534249740 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107736992 | AAACAGCATGGTACT[C/G]GTACCAAAACAGAGA | 10451 |
rs534252084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107696210 | TGGGGTACAGTGTGA[C/T]ATTTCAATATATGTA | 10451 |
rs534255329 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107910419 | CAGAATTTAGTAAGT[C/T]TATCTACATAAAATA | 10451 |
rs534263914 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107902056 | CTCAAAAAAAAAAAC[A/C]AAAAAAACAACAACA | 10451 |
rs534266212 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107749658 | GGTTATTAATTTTTT[G/T]GGGTATAAAGCAACC | 10451 |
rs534267355 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107935615 | TGCAGTTACAGAAAT[A/G]AGTAAGAAACCATCC | 10451 |
rs534273532 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755111 | ATGAATAAATGAATA[C/G]GAATCAGCCATGAGT | 10451 |
rs534274779 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107834382 | CCCATGCAGTGCTCT[A/C]AGGCAGGAATTTTAA | 10451 |
rs534275273 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107676056 | ACCTAGGCACAGTAT[A/G]CCCAAGGATGAAAAC | 10451 |
rs534293732 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107911751 | AAACAGGTTCTCAAC[C/T]GGGATATAACATCAA | 10451 |
rs534301761 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107807143 | CCACAGAAATTCTTG[A/G]TTTCTAGGTGTCAAA | 10451 |
rs534304754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894806 | TCCCCCATAGAAGTA[C/G]CCCTAATGACAGAGG | 10451 |
rs534304832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902539 | TAGATAGTCTTATGT[A/G]GGAGTTTTTTAGGTA | 10451 |
rs534309853 | in-del | -/TTATT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107702704 | TGCCATACTTGCGTA[-/TTATT]TTAAAGTTTGGTGCT | 10451 |
rs534317318 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107700794 | ATAGTAGAATGATTT[C/G]TATTCCTCTGGGTAT | 10451 |
rs534319529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107850595 | GGGCAAGGGGAGGGA[C/T]TGCATTAGGAGAAGT | 10451 |
rs534345667 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107711844 | GCATGCACTAGCATG[C/T]CTGGCCAATTTTTGT | 10451 |
rs534352146 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673647 | TCTTGTTCATTCTTG[G/T]ACACTTAACACCAAG | 10451 |
rs534353420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690513 | TGTGAGACCCAGACA[C/T]GGCACTGATGAGACT | 10451 |
rs534356326 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771532 | TGCTGGGATTACAAG[A/C]GCGAGCTACCGCGCC | 10451 |
rs534374034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942480 | AAAATTTCAGATCTT[A/G]TCTCACTTCTTCAGG | 10451 |
rs534381143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107577733 | GCATGAGCCTGAAAG[A/G]AACTGGATCGCTAAA | 10451 |
rs534387695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107718479 | CAAAGAGAATAAAAT[A/G]CCTAGGAATCCAACT | 10451 |
rs534398658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107770994 | TAAAATGTTCATAAA[A/G]TTGGAAACACCATAA | 10451 |
rs534401329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107630289 | CAGTTACATAGTAGG[C/T]ACTTTATAAGTATAT | 10451 |
rs534434207 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107853450 | TCAGAGTTTGCCATA[C/T]GTGCCTTTTACTTGG | 10451 |
rs534435856 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681722 | GCAGTGGCGCGATCT[C/T]GGCTCACTGCAAGTT | 10451 |
rs534464798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107680958 | TAAAAAGAAAGAATG[C/T]CAATGCATACATAAA | 10451 |
rs534496131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107718098 | AACCCACAGCCAATA[C/T]CATACTGAATGGGAA | 10451 |
rs534519134 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107770099 | CCCTCATTCTGCTCC[A/C]GCCACACTGGACTGC | 10451 |
rs534522924 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107862633 | CAATTTATTGTAAGC[A/T]AATGAAGACTCAATG | 10451 |
rs534546186 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107874438 | ACCCAACCAAGTATC[A/T]AAATAGAGAAAAGGA | 10451 |
rs534554698 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107892187 | TGGCAATCATTTAAC[A/C]CATGAGAGTCTTGGT | 10451 |
rs534555602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808257 | GAACATGGGCTATTA[C/T]TGAACACAGAAATGA | 10451 |
rs534556823 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107758267 | GTTCAGATCCTCACG[-/T]TTTTCAAACAGATAA | 10451 |
rs534580620 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107666633 | GGAATGCAGTGGCAC[C/G]ATCTCAGCTCACTGC | 10451 |
rs534589633 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107919147 | CAATAGTTATTCTAA[A/G]AACAAAACTTACATT | 10451 |
rs534598367 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107911214 | AGCTGGAAAATACAA[A/T]GAAGCATAAATTAGA | 10451 |
rs534600014 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107796066 | AAGCTTAATCTTTTT[A/T]TTTTTCAGGTCACAT | 10451 |
rs534605863 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587370 | TCAGGAAAAAAGAGA[-/T]TATCAGCATTGATCC | 10451 |
rs534630290 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107704672 | GGTGAAATAAGAAAG[C/T]GGTATATTAAACGGT | 10451 |
rs534654786 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722859 | TTTTTTTTTTTTGTA[C/T]GCTTACTAAGTAGTT | 10451 |
rs534664052 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107741721 | AAATATGAGAATGTA[A/G]GTGGGCCTTGAGCAC | 10451 |
rs534665152 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107740906 | AACCATTTACTCTCT[A/G]GCCCCCTACAACAAA | 10451 |
rs534669432 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107614945 | AATGTATAATATCCT[C/G]CCACCTGCCTACAGA | 10451 |
rs534671998 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107807522 | CAAGCCAGAAACAAG[A/G]GCAGGGTCGTAGTGC | 10451 |
rs534676078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107850097 | GAGGATATGGAGAAA[C/T]AGGAACACTTTTACA | 10451 |
rs534680036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802631 | TTGGTTAGGTAAAGA[A/G]GATACATTACATTTA | 10451 |
rs534689785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699913 | ATATAAGGGCGATTC[C/T]GGCTAAACTGACTTG | 10451 |
rs534700184 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107693122 | GAGAAGCTTGCATAG[C/T]GGAGTTCATACCTAT | 10451 |
rs534703216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699085 | CAATCATGCCTACCC[A/C]ACAGTCCCCCAAAGT | 10451 |
rs534718461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808734 | TAAGATGATTTTCTA[A/G]CTCCACAATATTCCA | 10451 |
rs534719598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107788781 | AAAGAATTGTTAGTA[C/T]ACAACCGTAAAAGAA | 10451 |
rs534729197 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713375 | TTTAAATAAAAAAAA[A/C]ACATAAAAAATTAGA | 10451 |
rs534741127 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107918199 | CACACACAGGCAGGG[G/T]TGGGAAAGATAGCAC | 10451 |
rs534741989 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107658664 | TGTGAGATGGTATCT[C/T]ATTGTGGTTTTGATT | 10451 |
rs534744188 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107734500 | ACAGGCTCAAAATAA[A/C]GGGATGGAGGAAGAT | 10451 |
rs534754613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795196 | GCTGATTTTCCTCCT[A/G]CCAGTCTCCAGGAAT | 10451 |
rs534762185 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107577168 | CCATGCTGAAAGTGC[C/T]ATACTCAGTATTTCA | 10451 |
rs534774226 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107667602 | AGGATTATTATACAC[A/G]CACACACACAAACAA | 10451 |
rs534800910 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107585833 | GAGGCACAAATGCTC[C/T]ACACACACTGTAGTT | 10451 |
rs534826919 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107806158 | CCTTCAGGCCCTTGT[A/G]CTGCTTCCTATGGGT | 10451 |
rs534846708 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957956 | CACCAAGAGGGTTTC[A/G]GTACTTCAGTGCCTT | 10451 |
rs534863607 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107636876 | AGTACTAACTAACTA[C/T]ACTAGCAAAAGAAAG | 10451 |
rs534865153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613456 | CTCCTCAATTTCCTA[C/T]ACAACTGTGTCTGAT | 10451 |
rs534873127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107644116 | TTCCCCTAAACAACA[C/T]TCTATAAGAGAACTC | 10451 |
rs534880072 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107775294 | ATGGGTTAAAAAAGA[A/G]TATCGACTGGGCACA | 10451 |
rs534881019 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664312 | GGGTATTAAGCTCAG[C/T]TTCCATTACCTATTA | 10451 |
rs534903186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940757 | TGTATGATTCCATTT[A/G]TATGCAGTATCTAGA | 10451 |
rs534909369 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933217 | TTGTCTTGTTTTGCT[C/T]ACAATACTCATATTT | 10451 |
rs534925711 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107880866 | TGCATTTATGATTAT[C/T]GGTGTTGTAGTGATG | 10451 |
rs534926982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107576167 | CCCCAACAGATAAAT[C/T]ATAGAATGTCTCATG | 10451 |
rs534942989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933897 | TAGGTAAAGCAATGT[C/T]TCCACAGTCATAAGA | 10451 |
rs534947869 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693639 | TGCTTAATAATATTT[A/G]GCCACATCCTATAAC | 10451 |
rs534972659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107829035 | CTCACATAACAAATT[A/G]CGGATGCTGGAAAGC | 10451 |
rs534986751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107877440 | CCCCACCTGTAGGGA[A/G]AGCTGCAGAAGACTT | 10451 |
rs535014037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107806520 | TTAAGTCTCCAATAA[C/T]GGCTTTTACTATCTT | 10451 |
rs535024891 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107871105 | TCTTTACATACAGTA[C/T]GGAAACGAACAAAGT | 10451 |
rs535032411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107678015 | GAAATCTGTTATCAC[A/G]GAAAAGGGAATCAGA | 10451 |
rs535034847 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107745923 | GAACTCAAGGGACTC[A/G]TGTTGATACTAAAGA | 10451 |
rs535046693 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107763560 | TTTTGAGTCACAGTG[A/G]CTCCCAGCTCTACAC | 10451 |
rs535049383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107650774 | GTCCATGTGTTCTCA[C/T]TGTTCAATTCCCATC | 10451 |
rs535055400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753828 | GCCTCCCAAAGTGCT[A/G]GGATTACATGTGTGA | 10451 |
rs535055957 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739505 | AATGTGAATAGGTCA[A/G]CACCATGAGACTCTC | 10451 |
rs535058773 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107583824 | TCGCGAAAATGGCCA[C/T]ACTGCCCAAGGTAAT | 10451 |
rs535068882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891035 | CCACTTGTATATATA[A/G]CTCCTTCTGCCTAAA | 10451 |
rs535075766 | snp | A/C | 0.0256215 | 0.110247 | intron-variant | VAV3 | GRCh38.p7 | 1:107849242 | AATTTCATATGCAAC[A/C]AAAAAAAAAAAAAAG | 10451 |
rs535075828 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107857319 | CCAAGCTTTTCAGCT[G/T]TGGCATTCAGACTAG | 10451 |
rs535083980 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107718381 | ATACAAAATCAAGGC[A/G]CAAAAATCACAAGCA | 10451 |
rs535085327 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107758141 | GTCATCACTTAAGCC[A/G]AAACCTAAAAGGTGT | 10451 |
rs535110883 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107836563 | TAGCAGAAGAAAAGA[A/C]ATAAAATCAGCGAAG | 10451 |
rs535113070 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107658064 | GGGCACAATACTTCA[A/G]TATCTCTTTCTAATG | 10451 |
rs535122136 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107670921 | AGGTGTTGCCATTTC[A/G]TTTTCTCAAAATCAT | 10451 |
rs535132356 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107856758 | AGTATGAAGGAAGGC[C/G]AGGCATGGTGGCTCA | 10451 |
rs535137628 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808688 | AGTGTTGCCCCAATG[A/G]TTCAGAGTATATACT | 10451 |
rs535140997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107614104 | TATCATCATCAGTGG[G/T]ATGGGTTTTCTCCTA | 10451 |
rs535142586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636758 | TTAAATCAAACCATC[A/G]TAAGGCAAGGACCAT | 10451 |
rs535152784 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107640238 | CATCAACAGGTTAAC[A/G]GGTAAACAAATTGTG | 10451 |
rs535162230 | snp | C/T | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688573 | GTAATTATTTTGCAA[C/T]CTTGGTTCTCTTACC | 10451 |
rs535163696 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107628839 | TTTGGCCCTTTAAAG[A/G]CACAGTTCTAAATGA | 10451 |
rs535167830 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575964 | AGTCATCTTTTCAAG[G/T]AATGTGTACTGAATT | 10451 |
rs535171375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107947663 | TGCATGAGTTGAACC[A/G]AGGTCTGGCCAATGC | 10451 |
rs535188638 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107612056 | CCATAGTCCATTAAC[A/G]CTGCAAAACTTCTGC | 10451 |
rs535191385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729513 | TTGGACAACAAACTC[C/T]CTAAAGAAAAGAATG | 10451 |
rs535197012 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764761 | ACTTCTTACTATCTA[C/T]GCAAGTTATTCATAA | 10451 |
rs535199080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710501 | CCAACAGATACCAAA[C/T]ACAGATTACTTATTT | 10451 |
rs535201571 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592481 | TAAATATAGTGATAG[A/C]CATTTAAAAAAATTA | 10451 |
rs535208259 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107956782 | TGAGAGCAGTCAGCA[A/C/T]GGTGCGGGTTTTCCT | 10451 |
rs535227355 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107848342 | AAAAATAGTGGCAAA[C/T]TGAATCCAGCAGCAC | 10451 |
rs535235460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963164 | TGCTGAGAGTTCCAG[A/G]AAACAAGTTCCAGGA | 10451 |
rs535236499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107949192 | AAATGAAGTTTAGCT[C/T]GTTGCATTTATATGT | 10451 |
rs535238267 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107783315 | ACATAGGGAACAGAG[A/C]AGGGGCCAGGAGACC | 10451 |
rs535256053 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107847679 | ATGAAGAAGAAATGG[A/G]TAAATTTCTGGAAAC | 10451 |
rs535259103 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107941512 | TCCGAGGCCAACATC[C/T]TTCGGGGCCTGTGAC | 10451 |
rs535264053 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107717599 | TGCACTGTGGTCTGA[C/G]AGACAGTTTGTTGTG | 10451 |
rs535264087 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107646961 | ACACTCCAAATGACA[C/T]ATGTGCTTTTTTTAA | 10451 |
rs535272238 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107643916 | GTTGAAAAACACTGT[A/G]CCCTTCACCCCAGTT | 10451 |
rs535279225 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107620499 | CTAGGTGTGTAGTAG[C/G]CTACACTATCTAGGT | 10451 |
rs535288346 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107723129 | TCTTATTTGTATTTT[G/T]TATCCTCATAAATGG | 10451 |
rs535291111 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107956404 | TGAGAATCCTCAGCA[C/G]CTTTTGTTTGGGGTT | 10451 |
rs535295578 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728851 | TTGTCACCAAGTATC[A/G]TTTTAATCTTGATAC | 10451 |
rs535299505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807409 | CTGATTTATCCTTTG[C/T]TCTTATATTGGAAAC | 10451 |
rs535316065 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107694425 | AAGCATTCTGTGAAT[G/T]GCTTCATTTTCTTGC | 10451 |
rs535317517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107627950 | AGGAACTGAGATAAA[A/G]TAATGAAACCCATAG | 10451 |
rs535319111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107760045 | ATAGAGATGACTAAT[A/G]ATTTTGCAGCTACAG | 10451 |
rs535322309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737205 | ATACAAAAATCAATT[C/T]AAGATGGATTAAAAG | 10451 |
rs535331205 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929822 | TGGATAAAGAAAATG[G/T]GGTACTTATACACAA | 10451 |
rs535332808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107926235 | GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC | 10451 |
rs535336355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107735077 | ACTGCACAACTACAT[A/G]GAAACTGAACAACCT | 10451 |
rs535347814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107828798 | CACATCTGCAAAGTC[C/T]TTTTTGCCATGTAAG | 10451 |
rs535352862 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107734366 | ACATAACAATATTAA[A/C]CTTAAATGTAAATGG | 10451 |
rs535353395 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107722559 | AAATGGACTTATTTC[A/G]AAGAACATTTACTGA | 10451 |
rs535370584 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107598212 | TACAAAAAAGTTAGC[C/G]AGGTGTGGTGGCAGG | 10451 |
rs535373199 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107583813 | AAGAATCAATATCGC[A/G]AAAATGGCCATACTG | 10451 |
rs535376177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107606793 | TGTCTGCTCACTCCA[A/G]TGGTTTCTTCTTTTT | 10451 |
rs535389009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107621817 | AACATTCCTCTCTCA[C/T]ACTTAGGTGTCATCT | 10451 |
rs535391840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107898703 | TGTAGGTATTTAAAA[A/G]TGTATCTCCTATAAA | 10451 |
rs535395486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672990 | ACATCTACATCCAAA[A/G]TCTAGGAGTTCATAT | 10451 |
rs535396665 | in-del | -/AGAC | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107846852 | CCCACTGTCAATATT[-/AGAC]AGATCAACGAAACAG | 10451 |
rs535406048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107949961 | GTTGTACTACTGAAT[C/T]ATAACATTACTGAAA | 10451 |
rs535421625 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107711567 | CAAATCCTTCTAAAG[A/T]TAGCAAATTCGAGCT | 10451 |
rs535434744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107614050 | GGGATACTGCTTTCC[C/T]TTTTTCTTTCCAATC | 10451 |
rs535435026 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107706024 | GCTTAGCTATTTAGG[C/T]TGCTGCAAAAGTAAT | 10451 |
rs535441301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738592 | CTAAGTTTCTCCCAT[C/T]GTTTCCATTGCAAGG | 10451 |
rs535443147 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107867195 | AGGACAATGGGATTC[C/T]TTGCAAAGTTATTTG | 10451 |
rs535446861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942386 | AGACCATATCCAGCC[C/T]TTGGCCTTACAAATC | 10451 |
rs535455758 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107704390 | TATGCAGAAAACTCA[C/T]GTAAATTTTAAGCAT | 10451 |
rs535459360 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107703854 | AGGACAAAGAGAAAA[A/C]AGAAGAAAGGGAAGA | 10451 |
rs535471005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698474 | TAAGCAAAGCTATAA[C/T]GTACAATAGGTTAGG | 10451 |
rs535503172 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107808195 | TCTTTAGTAGAAATA[C/T]GGGATACATATGGGC | 10451 |
rs535508481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933135 | AACCTCTTACTATTC[C/T]GAGGCCTAAATGACA | 10451 |
rs535511057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107576419 | GAGTGGAAGAAGGGG[A/G]AACAAAGCTGTAGTC | 10451 |
rs535520488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107581638 | ACCACAAAACACAGA[A/G]GAATGCCAATTAAAA | 10451 |
rs535522595 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107709961 | CAAAAAACTATAATC[A/G]TACTCATACATATAT | 10451 |
rs535524141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107800934 | CCCCAGTGTTTTCTT[C/T]GAGTAGTTTCACAAT | 10451 |
rs535536567 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794124 | ACAATGGTTGAAAAC[A/T]GACCCAGAACTGTCA | 10451 |
rs535540359 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107585078 | ATTTTGGATTGAGAA[G/T]GCTATGATTAGACTT | 10451 |
rs535544384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842209 | CCCTCTTCTTTAAGA[C/T]ATTGCTTTAAACATT | 10451 |
rs535552107 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921817 | GGCATTAAATATATC[A/G]TTTTGATTTTCTTAA | 10451 |
rs535568395 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107949544 | ATTCCTGGGCCCAAA[C/T]AATCCTCCCACCTTA | 10451 |
rs535569215 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575684 | TGACCTTGCATAGGT[C/T]TCCTAACCCCTCAAG | 10451 |
rs535575211 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107745107 | TATTTTCCAGCATGA[A/T]TATGAAAACCAGTTT | 10451 |
rs535577212 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107889042 | CCCATTCTTAATGAC[C/T]ACAGTAAATTATCTC | 10451 |
rs535582613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686394 | CATGGAGAGAAAGAA[A/G]GTCTTCAAGAGAGGA | 10451 |
rs535593616 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107575053 | TCGATGGCAGGAGAG[A/G]AGCTAACTTTCTCCC | 10451 |
rs535605214 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107933615 | CCCAGGAGTTAAGAG[A/G]CCAGCCTGGGGAATG | 10451 |
rs535616105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107871072 | CATAAACTGACGATT[A/G]AAACAGTTATGGAAA | 10451 |
rs535625198 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896551 | CTCTCCTGCATCTAT[A/G]TTTACTAGAAAGTCC | 10451 |
rs535632231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107574386 | AGGTGCAAGCAAATT[C/T]GCTTCATAAGTTTAA | 10451 |
rs535632299 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | VAV3 | GRCh38.p7 | 1:107583769 | GAGGATACAAACAAA[C/T]GGAAGAACATTCCAT | 10451 |
rs535636609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619792 | CAACAAAAGGCTTTA[A/G]TCTATAGAATGCAGT | 10451 |
rs535636980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107670772 | TTAATTTTAAGTCAC[A/C]CTACAAATATGAGTA | 10451 |
rs535637091 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107711183 | GATATTTAAAAGTGA[A/T]AAAACTAATGAGAGA | 10451 |
rs535650232 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946904 | ACTCTTTTATTAAGA[A/G]TTTACAACATTCAAA | 10451 |
rs535667802 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107782329 | ACCAGAAAAATGACA[A/C]CCCCTCCCCTACACA | 10451 |
rs535679663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107643265 | TGTGCCACTGCAATA[C/T]TTAAGACATTCATAT | 10451 |
rs535685379 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940012 | CAATAAGAGGCCAAG[C/T]AAGACGATTTTGAAG | 10451 |
rs535692792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107650672 | CATTAACTCATCATT[C/T]AGCATTAGGTATATC | 10451 |
rs535712673 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107771820 | AGTTAACAATTACAG[A/G]AGGCACAGATGATAT | 10451 |
rs535712731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716378 | CACGCCTGTAATCCC[A/T]GCACTTTGGGAGGCC | 10451 |
rs535713966 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658633 | CTGACTTTTTAATGA[C/T]TGCCATTCTAACTGG | 10451 |
rs535761395 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV3 | GRCh38.p7 | 1:107657945 | TACGAGAGGAAATAC[A/G]ACTAGAAAATCTGCA | 10451 |
rs535770497 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107748405 | GTTGATTTATTTTCT[A/C]CCTCTTTGTTGAGCT | 10451 |
rs535784946 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107684033 | ACTTAAATGAGAATA[C/G]TGTTTTAATTATAGA | 10451 |
rs535808929 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107842728 | ATTTTTACGCATTTT[A/G]ATTTTTCTTCTTGTT | 10451 |
rs535813048 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107883075 | ACAACTCATTTCTAA[A/C/T]GGGTAATTTTTTAAG | 10451 |
rs535830249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107832800 | TGTAAGCCATTGATT[A/G]CATTGTACAAAATGT | 10451 |
rs535850646 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107785088 | CTGGTGATATTGTAC[A/G]CTGATAAAACTACCC | 10451 |
rs535852877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107876796 | TAGATGCATTTTATT[A/G]TATGTAAGTTATACC | 10451 |
rs535856281 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107709579 | GATATGGTTTGGCTG[C/T]GTCCCCAACCCAAAT | 10451 |
rs535866194 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107958422 | TCTTTAAAATAATAA[C/G]AGCAGCATCAAAACT | 10451 |
rs535873287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794561 | CATTCTAAGTCTTTG[C/T]TGTCTTAAGGAGCAA | 10451 |
rs535882539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664908 | TCAGAAACAAGAGCA[C/T]GACCCAAGGTATAGT | 10451 |
rs535882633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657491 | ACTATAGAAAAGGAC[A/G]GCTAAGAAAGAATTG | 10451 |
rs535892018 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858248 | GGCTAAGATTAAAAA[C/T]GTGATCTTCATTTTG | 10451 |
rs535898254 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940651 | TTATTTAGCCTTAGA[A/C]AGGAAAGAAATTCTG | 10451 |
rs535905948 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628035 | TAGGACACAGTATGA[C/T]GGGTGTTATGATAGA | 10451 |
rs535944436 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant, nc-transcript-variant | VAV3, MIR7852 | GRCh38.p7 | 1:107897255 | TACATACATATGCCT[A/C]CTACTACTTTCATAT | 10451 |
rs535947451 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107752455 | TTCGAGATTGATAAA[C/T]GGGACTTTGTCAAAA | 10451 |
rs535955527 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107893905 | AGATCCCAAAATAGG[A/G]AAACTCTTTCATGAA | 10451 |
rs535955680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107660842 | TATTACAAAGCATTA[C/T]GTGTTTTACATTAGA | 10451 |
rs535959910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107839908 | ACAACACTATGCCCA[C/T]AAATTTGATAACTTA | 10451 |
rs535967708 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107667887 | TTCCTTGCTTGGAAT[C/T]GTAGCATCCCAAGGT | 10451 |
rs535969346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620447 | GTAACATGCGATACA[A/G]GTTTGTAGCCTGGCA | 10451 |
rs535969680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107890013 | CTTTTGATTTTATTA[C/T]CTGAGAAACTTATTT | 10451 |
rs535975240 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107813652 | TTTGAAAAATGTAAT[A/G]CATTATTAACTATAC | 10451 |
rs535985544 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571999 | TCCCAACATGTAACT[C/G]TCTCAGTCTTGTCAG | 10451 |
rs535987632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107617391 | TATATTTTCTTAATA[C/T]TAAAAAACATATTCT | 10451 |
rs535993365 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573235 | CAGCCAGAAATGCAG[C/G]TTTTTAAACACTTCA | 10451 |
rs536005809 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107674754 | ATACTTAATCCCCTT[C/T]CCTGAATGTGGGTAG | 10451 |
rs536011489 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107606207 | TGGCTATGAATATTA[C/T]TGCAATATTCATAGT | 10451 |
rs536018749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107627800 | AAAATACTTTAATGG[C/T]CTTTCAAATGACATC | 10451 |
rs536025672 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107716796 | TTCTGTTGACTGGAA[A/T]AATTTCAGAAGGAAT | 10451 |
rs536032263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756005 | TTCCTGAGAGCATTC[A/G]GTCAAGGAAACCGGT | 10451 |
rs536052470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107766245 | GTCCTTCCCCCTCCT[C/T]CTTCTTCTTCTTCTT | 10451 |
rs536056876 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107924937 | ATGTGTCCCAAAAGA[C/T]ATGTACGCATTCAGC | 10451 |
rs536067923 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107758524 | CCATGACTACACCAT[C/T]GCACTCTAGCTTGGG | 10451 |
rs536071605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107944643 | AGAGTCTCACTCTGT[C/T]ACCCAGGCTGGAGTG | 10451 |
rs536087335 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107916199 | CAAAAAAATATATAT[A/C]TGAAAAGAAGAAAAA | 10451 |
rs536101539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862605 | CTTACATATTTCTCA[C/T]CCATCATATTTACAA | 10451 |
rs536106212 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893150 | ACAGCCAGTTATTCT[A/G]TCACGAACATTTTCA | 10451 |
rs536110978 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107728324 | AGGACCTGGTTCCTT[C/T]AATAGTCTCAGTTCC | 10451 |
rs536111227 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107854389 | ACAGATACATATTTA[C/T]CTTATTACTACCTTG | 10451 |
rs536119747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107899795 | AACTAATAATAACTG[A/G]TGAATTAGGTTTTGA | 10451 |
rs536121031 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107634660 | TTCTGCACAGCAAAA[A/G]AAACTACCATCAGAG | 10451 |
rs536126604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107810022 | TTTCTAGAAGTTTAT[A/G]TGTTTATAAAGACCA | 10451 |
rs536127806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107674089 | AATAATCTGAAGGTA[A/G]TTTTTCAGAACTGCA | 10451 |
rs536152865 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590504 | ATGTGAACTATGAAA[C/T]GGAGTATTAATGATT | 10451 |
rs536174288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107727344 | TAAGATGATGAATAT[G/T]ATCTCCACAATTAAA | 10451 |
rs536181220 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769252 | CCTTCTCTTCTTCCA[C/T]TGTGCTTTTCTAGAA | 10451 |
rs536189123 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107954284 | CTTCCCAGAGAAATG[G/T]AGGCACTCCTGACTC | 10451 |
rs536189139 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107820273 | CAATAGAGTACTATT[C/T]GTCCATAAAAAAATG | 10451 |
rs536191704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769961 | CCACTCTTGCCTCAG[A/G]AGAGCCAGAATGAGA | 10451 |
rs536198734 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587320 | ACCTTATGCAGATTT[A/G]GGATTCAGCAGGGAA | 10451 |
rs536205320 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107758185 | CTGTTCTCTCTCCCT[-/C]ACTATGTCCTATTGA | 10451 |
rs536213284 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965260 | GCGCGCCGGCGGCCG[C/G]GGCTGGGGTCTGTGG | 10451 |
rs536220181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107825900 | CAATGTTGTAAATTT[A/G]TCTACACATTTACTA | 10451 |
rs536224793 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107742652 | CCATTCCCAGATCCA[C/T]GAGGCTTTCTTTTCC | 10451 |
rs536226816 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769818 | TCTCTTTTTTTCACA[A/T]CCTTTACTTAATTCA | 10451 |
rs536231394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107638590 | TCAGTCTTGTTAGGA[C/T]GTCAATTTTCCTATA | 10451 |
rs536234475 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695602 | AGGTCAATGCAAGAC[A/C/G]CATGGGAGGGGATAT | 10451 |
rs536235197 | in-del | -/A | 0.129322 | 0.218945 | intron-variant | VAV3 | GRCh38.p7 | 1:107639381 | ATTATCAAGAGAATA[-/A]AAAAAAAAGCCACAG | 10451 |
rs536236733 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107638854 | AATGTAACAAAATAA[A/C]AGTCCAGAAACAGAC | 10451 |
rs536248834 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107798336 | TCACACCTGACCACT[A/G]CTCAAGGTGGCTCCT | 10451 |
rs536252294 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107653505 | CAAACTCTGAGGATC[C/T]GCAATCACCACAATA | 10451 |
rs536257141 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966108 | CCTCAAAACCACAAT[A/T]AATGTTTAAATTATT | 10451 |
rs536264461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107873796 | GCAGGCAGCCTGATG[C/T]CTGAGAAGGCTGGTG | 10451 |
rs536264640 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107745192 | GAGACAGTTAGTGAC[-/A]AAAAAAAAAATAAAA | 10451 |
rs536265978 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107866276 | GCCCCTCAGTCGAAT[G/T]CTTTCTTCTGAGGAG | 10451 |
rs536266556 | in-del | -/AC | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107661017 | TAAATATATCTATAT[-/AC]ACACACACACATAAA | 10451 |
rs536288352 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107913843 | CTCTGTTGCCCAGGC[C/T]GGAGTGAAGTGGCAT | 10451 |
rs536289159 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107906424 | AATCCCAGCACTTTG[A/G]GAGGCCGAGGTGGGC | 10451 |
rs536290694 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107655063 | AAACTTTTATTTCTG[C/T]CTCATTTCTCAACTA | 10451 |
rs536292201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107645787 | TTACAGATGTTCATA[C/T]TTCGAACAGTCATTT | 10451 |
rs536303432 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107653747 | CATAGGAGGAGGCTA[A/T]CTATGTGTCTTCATT | 10451 |
rs536313463 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107679405 | AACTTAAGATCAGAA[A/G]GAGTGTAAGCTATTT | 10451 |
rs536320091 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649377 | TTGCTCTTACAGAAC[A/G]TGGAAGCAGGAGGCA | 10451 |
rs536321295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107845654 | ACTTCATGAAGCATA[C/T]ACAAGTATCAACAGC | 10451 |
rs536322828 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107622144 | TCAAACTAAAATTAT[C/T]GACAACTTCTTCTGA | 10451 |
rs536341040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832357 | GAGAGTCAGCAAATG[C/T]ATCGGCAGAGCAGTT | 10451 |
rs536345332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107886520 | CTCAGGAAAACATAC[C/T]ACAACCAACTTAAAT | 10451 |
rs536350075 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107749728 | CATACACTGAAAACA[A/T]CGGGGTATTTGAGGT | 10451 |
rs536352028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107741551 | TGACGCCTGTTGGCA[C/T]TACAAAAAATAGACT | 10451 |
rs536365073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107652841 | CATTTTCCAAAAAAA[A/T]AAAATTGTTTTTGAC | 10451 |
rs536369818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107740607 | CTGATACTAAAAATA[A/G]AAGAAAAAAAAAATC | 10451 |
rs536375044 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107620773 | GAGAACCCAAAGAAT[-/AA]AAGAGTAGGAAAAAG | 10451 |
rs536384622 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107855191 | CTATGTACCCCAAAA[C/G]AAGAAGAAATGGGTT | 10451 |
rs536389116 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880326 | ATGCTCCAGTCAAAC[A/G]GCAAAGAATGTGCAT | 10451 |
rs536395195 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872377 | ATACACATGAATTCC[A/C]GATTCACCAATGTAG | 10451 |
rs536404705 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107616805 | AAATATAGCAAGCAC[A/G]ATAGATTAAGGAGAG | 10451 |
rs536406762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107893362 | ATAAAAATCACAGGG[C/T]AAAAGTGTTTACTTA | 10451 |
rs536419285 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667442 | ATGCCTGTAATGGGG[C/T]AGCAATGCAGGAAAT | 10451 |
rs536436733 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107661521 | TATATTAATTTTGTT[C/T]TGCTTTCTCCCCACT | 10451 |
rs536438603 | in-del | -/GGGAG | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950827 | CAACTAAAGAGCACA[-/GGGAG]GATAATGGCTTAGTA | 10451 |
rs536443525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107851667 | AAAGGGAACAGGCTC[C/T]GAAAAATAATTCTTG | 10451 |
rs536446492 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107600518 | TCTAATAGTGGCATT[A/G]CTGAGATTTTATACA | 10451 |
rs536453784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632141 | CTACGTTTAATAATA[C/G]CAATTACCAACTGGT | 10451 |
rs536458953 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879289 | AGAATACAAGAGCCA[A/T]TTACATGAGAAGAAC | 10451 |
rs536459725 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107936796 | ATTCCCTGCACTTCC[C/T]TTCCTGGTTGGAATT | 10451 |
rs536480886 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107615832 | TACATATAATTGGCC[A/C]AAAAAAATTTGAAAA | 10451 |
rs536482310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107844873 | AGGTGCAGCTGTGGA[C/T]GCAGCTTCAGCAGAC | 10451 |
rs536497807 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719002 | GAAAACTGGCTAGCC[A/G]TATGTAGAAAGCTGA | 10451 |
rs536505121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107725698 | TTTGTATTTTTAGTA[C/G]AGATGGGTTTCACCA | 10451 |
rs536508959 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107850727 | AAGTATAATTTTTTT[A/T]AAAAAAAGAAAGAAA | 10451 |
rs536511798 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107712031 | AAGCTCCTAAATAAG[A/G]AAATGGAATATTTTA | 10451 |
rs536534016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107666593 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCACTCTGC | 10451 |
rs536536611 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107603458 | AAAAAGACAGTTGTG[A/G]GGAGCTTAGGGACAG | 10451 |
rs536536912 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755331 | AACCTCCAACAGTAG[A/C]AACTTGAAGGTAAAC | 10451 |
rs536539837 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107658819 | TTATCTTGTAAATTT[C/G]TTTGAGTTCATTGTA | 10451 |
rs536547897 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747332 | TCCTTCACTCATCTG[A/C]AGATTATATAGCCAA | 10451 |
rs536572956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107622652 | ATGAACGATTGGAAA[C/T]TCTCCCAAGTTACAA | 10451 |
rs536585138 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107754536 | CTGGCTGGGCTGCCT[A/G]CTCACAGGGTCTTCT | 10451 |
rs536590160 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107775946 | GACTAACAACCTCTG[C/T]TCTAGAATAAGAGGT | 10451 |
rs536601230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107748897 | ATTAGAGTACACTTA[C/T]TGGTTGTTCATTATT | 10451 |
rs536611308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107839121 | GAAAGAAAAGGAAAA[A/G]TTAAAAGAATACTGT | 10451 |
rs536611323 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107831460 | GAAATTTTTCTTCCA[C/T]ATATATTGCAATGTT | 10451 |
rs536631697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107586731 | GAAGGGGAAAGAACA[C/T]ACCAGATGAAAAGTT | 10451 |
rs536637123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107957506 | GTCAGTATGAATTTG[A/G]GATCCAGCAAGGTAG | 10451 |
rs536647647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950797 | AGATGGACCAGGAAA[A/G]GAGGAGATATCAGTC | 10451 |
rs536655383 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107713966 | TTTAACGTTTGTGCC[A/G]AATGTTCAAATACTA | 10451 |
rs536669791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107958071 | ACAACTACTTTACAT[A/G]AAAAGATCCTGATTG | 10451 |
rs536671468 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107858512 | GGAGGTGAGCAGTGC[A/G]TGAGTGAGCATTACT | 10451 |
rs536672310 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107730909 | CAGATTGAGATGCAA[A/G]CTCAGCTTCTGTCAT | 10451 |
rs536676739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107796851 | GGACCTTTTAAAATC[A/G]TAAGTGCATACTGAT | 10451 |
rs536688554 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107909870 | TATTTCATAATAATA[-/T]TTTTCTTTCAACTAT | 10451 |
rs536691755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107637792 | CTAGATCCCAATTCA[C/T]TCCTTGAACATTACA | 10451 |
rs536702100 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858879 | CTTCAAATGTTCTTG[A/G]AACTATACAGTTGTT | 10451 |
rs536703927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107644970 | GTATACAGAGTATAC[A/G]CTAGTATACTCTGGT | 10451 |
rs536704921 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107871083 | GATTGAAACAGTTAT[C/G]GAAAATTCTTTACAT | 10451 |
rs536707914 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572396 | ATCTTTGTGTGTGTG[C/T]GGGGGAGGTGGATGG | 10451 |
rs536711272 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107851573 | AAAAAGTCACCACAT[A/T]CCCTACACTTGTTAA | 10451 |
rs536717059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107803970 | TTTCCTGCTGAATTG[A/G]CCCCTTATATTATTA | 10451 |
rs536719961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107920026 | GTGGTAATCTTTTCT[C/T]TCATAATGTCTGACC | 10451 |
rs536733072 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107730330 | TTTATTTAACGATCA[C/T]CTGAATCCACCCTGA | 10451 |
rs536748501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107838318 | ACAGACCCTTCTCAA[A/G]AGAGAACACACAAGT | 10451 |
rs536751272 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907659 | CTCTCGTGTGCGTGC[A/G]TTCTCTCTCTCTCTC | 10451 |
rs536764833 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842637 | TAGCTCAATGAGATT[C/T]CATTCTTCTTTTTTT | 10451 |
rs536771082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107701053 | TCTCTAATGATCAGT[A/C]ATGTTGAGCTTTTTT | 10451 |
rs536772417 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107767096 | CAAACATGTAAATTT[G/T]TACTTTGGTCAATTA | 10451 |
rs536776967 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107694220 | GCTACCATTGGATGG[G/T]CAAGGTACGGTTAAT | 10451 |
rs536779442 | snp | C/T | 8.34843e-05 | 0.00646028 | missense, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964716 | GGTTGATGGAGTGCG[C/T]CCGGAGGTTGTTAAG | 10451 |
rs536794489 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107862077 | GCATTATAATTGGCA[C/T]TGAGGCAAACCAGAG | 10451 |
rs536795964 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107793962 | GCCAAATCCCAGAGA[C/G]GCAGATCTAGCTTGA | 10451 |
rs536810743 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107858480 | CCCCCAGACCAGTAC[C/T]AGTCTGGTACACAGC | 10451 |
rs536826646 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107718964 | AATGGTGAAAGGATT[C/T]CCTATTCAATAAATG | 10451 |
rs536827768 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107577835 | GAAATAATTATCTTC[C/T]TGAAGCCTATTTAAG | 10451 |
rs536829180 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107935734 | GGGAGGCACACAGGA[C/G]AGGCACCAAAAACAG | 10451 |
rs536830303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107927386 | CTGTGGTGGCTATGG[A/G]GAGAGATGCCTTCTG | 10451 |
rs536830638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700579 | GTTCCTGCATTAGTT[C/T]GCTGAGGATAATGGC | 10451 |
rs536834019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107783089 | AGAAGAGTGGCATCT[A/G]TAAAGAAATGAAAAT | 10451 |
rs536836658 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107608830 | TGCAAACCCAACTAG[A/T]ACTATATATTCCCAG | 10451 |
rs536840279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107705802 | AATATCACTAGTTTA[C/T]AAATAAGAAAACTGA | 10451 |
rs536842981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107850221 | CAATCCCATTACTGG[A/G]TATATACCCAAAGGA | 10451 |
rs536848343 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107673368 | TTTGTGAATGGCTCT[C/G]CTGCTCCAACCCTAA | 10451 |
rs536862325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107928167 | CAAAGACCATCAAGG[C/T]GGTGCCTCTACAACT | 10451 |
rs536863273 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769361 | TCGTCTAATTTTCAA[C/T]ATGACCACAAAACTC | 10451 |
rs536866129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943434 | TTATCATTTCCTTGG[C/T]TTGTCTCTCACAATT | 10451 |
rs536868502 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893457 | AATACCTGAGACTGG[A/G]TAATTTATACAGGAA | 10451 |
rs536873653 | in-del | -/AGA | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107925204 | GTTGACGGTCAAGAT[-/AGA]AGTACCTTTGAGGCC | 10451 |
rs536889022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107809424 | TTTGTCCTTGGATAG[C/T]ACAGTCAGCATGGCA | 10451 |
rs536910063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107705340 | ACAAATGGCCACATA[G/T]GTCAACCTGCCTGGA | 10451 |
rs536923019 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107815823 | CACAACAGTCTCCAA[A/C]CTTTTTGGTACCAGG | 10451 |
rs536930693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107688088 | ACGCATCTACCAACT[C/T]CTGGCGATAAGGGCC | 10451 |
rs536932750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912949 | ATCCTTAGGATCAAG[A/G]AAGTCAACATGCCTA | 10451 |
rs536934810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107905682 | TTCAGTTGATTCAAT[C/T]TTATTGATTTTAGGA | 10451 |
rs536950274 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891665 | CCAACATGGTGAAAC[C/T]CCGTCTCTACTAAAA | 10451 |
rs536961331 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107822949 | GACAAAAGACAAGTA[A/T]GCAAATAAACAGGCC | 10451 |
rs536969543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107898988 | GAGATGAACTAGATG[C/T]AATGCCTTCTCTCCA | 10451 |
rs536972321 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889224 | AATGCCCAAAAACCT[C/T]CAAATTCTGTTATTG | 10451 |
rs536986218 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107741386 | TGTCCGGCCTGACTA[C/G]CCGCTCCCTGAAGGG | 10451 |
rs536987843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950144 | ACAAAAAAAAAGTAC[C/T]TCTACTGTATAGTGT | 10451 |
rs536989085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107884833 | GAAAGCTTGCAAGGT[C/T]CTCTACTTAGGGCAT | 10451 |
rs536994589 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107687551 | AAAAATGTTTTGCTA[C/T]GGCCATTTGTGGGGA | 10451 |
rs537007431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879430 | TTCTTTGTGGAGTGC[A/G]TAATAAGCCAATTCT | 10451 |
rs537008790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886408 | ACGCAGCCTCTCGGG[A/G]AGGGGTTCTACAGCA | 10451 |
rs537017887 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107828626 | TCCAGATATTATGGA[C/T]ACATAGCCCTCTTCC | 10451 |
rs537039389 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107745767 | TCCTATAAACAGAAT[C/T]GCCATCTTCTGTAAA | 10451 |
rs537039823 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600436 | CCCTTCCCTTTAACA[C/T]GCTGTGATACGTGCT | 10451 |
rs537045099 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880142 | GTTTGGCAAGTGCAA[C/T]GAAGAATACATTCAG | 10451 |
rs537069050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693802 | AGCAAAGGAGCATAT[A/C]ATCTAACAGGGGTAG | 10451 |
rs537071039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783028 | ACTAGAGTAAATCCA[C/T]GTCATGAATTTTCTT | 10451 |
rs537073683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667751 | AAACAAACAGAAGCA[A/G]CATTTATTACATTAG | 10451 |
rs537074578 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107774650 | TGTCTGGCGCCCTGA[G/T]ACTAAAAGGACACTG | 10451 |
rs537080120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107929264 | CTGCACTCCAGCCTG[G/T]GTGACAGAGTGACAC | 10451 |
rs537084956 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107652656 | TGCCTAAATTTGTAT[C/G]ATAAACATTTATTTT | 10451 |
rs537094288 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912090 | GTGTTTACGTTAGTT[G/T]CCTATGAAGAATGAA | 10451 |
rs537115136 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107796275 | GCTCTCATCTCTAAA[C/T]TGAGTGGCATGGGTT | 10451 |
rs537115528 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107824423 | GAGGATGGCCCCATA[C/T]GGAGGTTCAAATGGA | 10451 |
rs537119390 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107676815 | TGCAAAAAATTCTCC[C/T]TCATCTGCCTTCACA | 10451 |
rs537131921 | in-del | -/T | 0.464309 | 0.12873 | intron-variant | VAV3 | GRCh38.p7 | 1:107876947 | GTTTATCTTGGTTTG[-/T]TTTTTTTAATTTGCA | 10451 |
rs537138775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755844 | AGAAATTCCAAGCAC[A/G]TTAATTACTGACCTT | 10451 |
rs537139578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821657 | GGAGGGGCCAGGACA[C/T]GCATGGAAAAGCCAA | 10451 |
rs537143431 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107845634 | CTGAAAAACACAGCA[C/T]GAGAACTTCATGAAG | 10451 |
rs537181857 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107823661 | TGTTTGTATCTCCAC[A/C]AAACTCCTATGTTGA | 10451 |
rs537192570 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107871261 | AGAAAGCCAGAAAGA[C/G]ATTCATCTTTTTTCA | 10451 |
rs537193124 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107831819 | TTTAGACATATTCTC[A/C]TGTAACCATAGTAAA | 10451 |
rs537202550 | snp | C/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107587986 | ATTCTAAGATCATAA[C/G]TACTGCTCTGAGCCT | 10451 |
rs537210228 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107899788 | AAAGCCAAACTAATA[A/T]TAACTGGTGAATTAG | 10451 |
rs537215863 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107761987 | TTGATAATAATTATG[A/G]CTTTGAGTAAATTAC | 10451 |
rs537218355 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673559 | TTAAGTATACCCTCT[A/G]TATCTCCCTGATCTC | 10451 |
rs537219086 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107665733 | TCTTGCAGGCCAATA[A/C]TAGAAACACTCTGTC | 10451 |
rs537237772 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107795584 | TATGTAAGATGTTTT[A/G]GAATCTGAATGATCT | 10451 |
rs537239585 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107835733 | AAAAACCCCGGCCCA[C/T]AGGCACCATACCATC | 10451 |
rs537245593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107950633 | CTCTCTGCTGCTCAC[A/G]GGCAAGGGCAGCAAA | 10451 |
rs537252192 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107877526 | AAACAATATGAAATA[G/T]TGCATGCACAGAAGA | 10451 |
rs537258415 | snp | A/G | 0.000709425 | 0.0188204 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107704599 | TCCCAAACATTCTTT[A/G]TGTGCTCTCGCTCCA | 10451 |
rs537276578 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107850669 | GGCACATGTATACCT[A/C]TGTAACAAACCTGCA | 10451 |
rs537279847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107926518 | CTGGTTTTAACTTCA[C/T]CACTGAAAGCAGCAC | 10451 |
rs537292918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107857625 | CTTCTTGCGGGTATG[C/T]TCTTTTGGACAAATC | 10451 |
rs537296244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107576904 | CAAGAAAATTATTCA[C/T]ACAATTTGTTACAAA | 10451 |
rs537303219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107637709 | TTCCCTAGTAAATTC[C/T]ACGACACACTTCAGG | 10451 |
rs537312561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794761 | GTCATTAGCTCCTCT[A/G]ACTGTATGTGGTTAA | 10451 |
rs537319745 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107631128 | CTTATTTGGTAACTA[C/T]CAAAGCCAAAGTATT | 10451 |
rs537321613 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951375 | CTCCATTTTCTCTTC[A/G]CCCCCTAAAAGTGGG | 10451 |
rs537332549 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107958050 | CTTAAGATGCCTAAA[A/G]ATGCCACAACTACTT | 10451 |
rs537335339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107615823 | AAGAAGACATACATA[C/T]AATTGGCCAAAAAAA | 10451 |
rs537338089 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107890307 | AAATACCACTACTTC[C/T]ATGTAGTATTTCTTC | 10451 |
rs537339795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107665091 | GGAGAGGCCATGCTG[C/T]CTCTCCTTTAGGTAA | 10451 |
rs537339947 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753707 | TGGGACTACAGGCAC[C/G]TGCCACCATGCCTGG | 10451 |
rs537352287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672162 | CAATCTCAGCTACTT[G/T]GGTGGCTGAGGTACA | 10451 |
rs537360255 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107924770 | AAAAAAAACTGTGAC[C/G]ATATGTTCCCTGAGA | 10451 |
rs537365759 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815298 | ATCAGGCATACCAGC[C/G]CCAGACTAACTTGGG | 10451 |
rs537376206 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107785691 | AAGAGGGAACTGGGA[A/G]TGTGGGCATGAGTGC | 10451 |
rs537382902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760712 | TGGAATATCTGCAAT[A/G]TAGTTGATGCTTCAT | 10451 |
rs537418872 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107868643 | TATTTTATTATTTAC[A/C]TGCTGCAAAATAGGT | 10451 |
rs537434355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589721 | GATGACAAAAAAACT[A/G]AGGATACAATAAAAT | 10451 |
rs537441243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592736 | AGATGAGAAAGCTAA[A/G]GTCCAGACAGGCTAA | 10451 |
rs537454444 | snp | G/T | | | intron-variant, utr-variant-5-prime | VAV3 | GRCh38.p7 | 1:107754842 | ATCTTCGTGTGGCTG[G/T]CTGCTTCTTATCTGC | 10451 |
rs537461171 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107919777 | CTTAACAGTTAAACT[A/G]TCTTATGAAATCACC | 10451 |
rs537474140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107608798 | GTAAAAAATATCAGA[C/T]AACTCACATGGTAAC | 10451 |
rs537477988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599923 | TGTTATTTGACTCCA[A/G]CATGATAAAAGGTAA | 10451 |
rs537488014 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107640938 | AATTTAGGAGTCAAA[A/T]GCCAGCTGATGGAAT | 10451 |
rs537488599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107908948 | AATAACAAATACTTG[C/T]TACATAAGTACAACA | 10451 |
rs537493912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107648366 | TTTCACCTTTATTAA[A/G]AAGGTGTTTATAGGC | 10451 |
rs537504745 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107808845 | AATCAATGAAAATAA[C/T]ACTGCTGTATCAAAA | 10451 |
rs537504883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107778937 | GGAGATGACATACTA[C/T]ATTTAACCAATTTAC | 10451 |
rs537516353 | snp | C/G | | | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963859 | CTTCCACTGAACTGT[C/G]ACTTTTGAGCTGACT | 10451 |
rs537523890 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107735175 | GAGAACAAAGACACA[A/T]CGTACCAGAATCTCT | 10451 |
rs537530176 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107830039 | AACTCCTTAACCAAA[G/T]ATTTAGATTCCCCTT | 10451 |
rs537546868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915917 | GAAAATTAGACACTA[C/T]ACAAATAATAACAAC | 10451 |
rs537552917 | in-del | -/CATCAT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107636754 | ATCATTAAATCAAAC[-/CATCAT]AAGGCAAGGACCATC | 10451 |
rs537561820 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107658726 | ATTTTTTCATGTGTT[C/T]TTTGGCTGCATAAAT | 10451 |
rs537563596 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107919270 | TATGGAACTATTATA[C/T]TACTGCTCATCAATT | 10451 |
rs537565131 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107737584 | GAAGACATTTATGCA[C/G]CCAACAGACACATGA | 10451 |
rs537568555 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107829147 | GTAAAATAAACTAAA[C/T]GATTTGTGAAAAGAA | 10451 |
rs537576863 | in-del | -/TTA | | | intron-variant | VAV3 | GRCh38.p7 | 1:107801954 | ATGTGTTTCTTTTTT[-/TTA]TTATTATACTTTAAG | 10451 |
rs537580935 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107697190 | GGCTACTGATGGAAT[C/G]ATACAGAGATTCTTC | 10451 |
rs537585499 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699973 | TGATCACACACCAAA[A/G]GTTATGAGGCTGAGG | 10451 |
rs537595730 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107878215 | CACTTGACTCCTAAA[C/T]ACTCTGACTCTACCT | 10451 |
rs537601844 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107743691 | CTGGTATTCAAAATA[C/T]CTGAGCAATATCTTT | 10451 |
rs537603541 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871990 | AAAGTATAAGTAGAT[A/G]CCAAGTAACACATCA | 10451 |
rs537605177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107836634 | CAACAAAAACAAAAG[C/T]TGGTTCTTTGAAAGA | 10451 |
rs537626341 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107735377 | CAGAACTGAAGGAGA[C/T]AGAGACACAAAAAAC | 10451 |
rs537644260 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786100 | AAAGCAAAGCAGTAC[A/T]GCCAGATAAGATCAA | 10451 |
rs537646928 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107705179 | CTGATTCAAGCAAAA[C/T]GACTACTAAATGTGC | 10451 |
rs537647781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711452 | GCACAATGAAATTCA[A/G]TACCCCTGGTACACC | 10451 |
rs537649457 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107762938 | AGGTAGGATGAGCCA[C/G]GCTGATAGGGCAAGA | 10451 |
rs537652423 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881926 | ACAAAACTCTGAATC[A/G]CTCCTTTTCCTCTAC | 10451 |
rs537675990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107935052 | TTACGCGAACTGATG[A/G]GGCAAGTTTCCGGTT | 10451 |
rs537677947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795273 | ACCAAGATAACTAGC[A/G]TCTAAATAACTTAGT | 10451 |
rs537695223 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107883263 | TTGCTCTGCAGCACC[C/T]GGCTCACATCTGTTA | 10451 |
rs537697253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107941543 | GAGCTACACCTTTTT[A/G]TGGACACTTAAAAGA | 10451 |
rs537698878 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902494 | CCCTGTTTTCTGCCC[C/T]TTCACTATTGCCATG | 10451 |
rs537700458 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903785 | AACTAAATTTATATT[A/T]TCTGAGAACTGACAC | 10451 |
rs537711008 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107849145 | GAAAATGGCCATACC[A/G]CCCAAAGTAATTTGT | 10451 |
rs537713182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107801879 | TTCAATCCATGAGCA[C/T]GGAATATCTTTCCTT | 10451 |
rs537718406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107798493 | GGAGGCTGAGGTGGG[C/T]GGATCATGAGGTCAG | 10451 |
rs537727113 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107621272 | CAGAGAGGTGAGAGA[G/T]AATTTAACCTATTTT | 10451 |
rs537736864 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107887446 | ATTCTTTGGGATAGA[A/C]ATCTGCCCAACACAT | 10451 |
rs537741300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107661791 | GTCAAATTCTCTATT[G/T]CAAATAAGGAATGGC | 10451 |
rs537743056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750621 | AACAATCATTGTCAA[A/C]CACAAAAACCTCTGT | 10451 |
rs537746259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808070 | TTCTTGCATAGAAAC[A/G]ATGCTTTCTACATAC | 10451 |
rs537775622 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107888012 | AAAAATTTGGGGGGG[G/T]GGTTATTTTGTAAAG | 10451 |
rs537780144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107749930 | TTTTTAATTTAAAAG[C/T]TAAAAACCTATAGAA | 10451 |
rs537781728 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757617 | TTATGAAAGATTCCA[C/T]AATGATTAAAATCAC | 10451 |
rs537795105 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107577283 | TGTGACTCCAGGGTA[C/T]CTGCTCTTAGCGACT | 10451 |
rs537797062 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107609205 | GTATATATTAGTTAT[G/T]ATGACATCATGACTA | 10451 |
rs537814173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625175 | AATGCCCCCACAGTA[C/T]TCCACTCAGTCATGG | 10451 |
rs537816798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757135 | TATATATATGTTTGT[A/G]TATATATATGTGTGT | 10451 |
rs537818292 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107675586 | TTACTCCTTTATTGC[C/T]GTGAAGCAGGTAGTG | 10451 |
rs537840864 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107635955 | TCTATAAATTGAGGA[C/T]AATAATAGTAATTCA | 10451 |
rs537842030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597273 | GTTTCTTCTAAAAAT[C/T]CCACTGCCATCAACT | 10451 |
rs537845861 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107695863 | CCATGGATCTGTCCA[C/T]TAAAAGGTAGAGTAA | 10451 |
rs537847061 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953083 | TTCCTCATGCAATTT[A/G]CCATCTATCCACTGA | 10451 |
rs537863373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107763961 | TAAGAGCTGGCTATA[C/T]ATCTCTACCTGAAAT | 10451 |
rs537863797 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953762 | AGGGAAGCACGACGC[A/T]TGTTTATTCAGACCA | 10451 |
rs537867582 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107604513 | TCTCCAGCCTTCTTT[C/G]AGATCCAGGAGTTTC | 10451 |
rs537869275 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945415 | TTATATAGTTATTTA[C/T]ACATTCCTCCATATT | 10451 |
rs537870002 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107733132 | AAACTCCAACAGACC[C/T]GCAACTGAGAGACCT | 10451 |
rs537870231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107697672 | CATATATTTATGACC[C/T]TGTTTCTTCATCTTA | 10451 |
rs537886899 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107916699 | GGGATGGTTGGAGTG[G/T]CTCTTTTTTGATCAC | 10451 |
rs537886920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107648892 | GTTTCAGGATGATCT[A/G]AGTACCCGCCACATG | 10451 |
rs537899363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107633140 | AAAACATGAAAATAA[C/T]TGAAAGCACCATCTA | 10451 |
rs537909384 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107915357 | AAACCCAAAAACACA[A/T]GAGCCAAGAGAAACA | 10451 |
rs537910286 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726359 | ATTCCGCCAGAAAGT[C/T]CTCTGTGCTCCGGCA | 10451 |
rs537911832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632207 | TACCAATTAGATAAT[A/C]AAATCAATGGCTCAC | 10451 |
rs537914786 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107941875 | ATGATCTCCCCTACC[-/A]AAAAAAATGCATTAT | 10451 |
rs537927069 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107826356 | AACTCACATTTCTAA[C/G]GTTGAATATTTGTTT | 10451 |
rs537931370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107732776 | GTAGACTCCACCTCT[A/G]GGGGCAGGGCATAGC | 10451 |
rs537936904 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889992 | TTTTCTTTATTGTAT[C/T]ACCTGCTTTTGATTT | 10451 |
rs537943401 | in-del | -/A | 0.49533 | 0.0480965 | intron-variant | VAV3 | GRCh38.p7 | 1:107948321 | ACTTCCTGATATTGT[-/A]AAAAAAAAAAATTGT | 10451 |
rs537949483 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107944853 | TCTGGCAATCCGCCC[A/G]CCTCGGCCTCCCAAA | 10451 |
rs537953760 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603894 | CCTGCAACCTCCGCC[A/T]CCTGGGTTCAAGGGA | 10451 |
rs537963758 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107834288 | TCTGAATGTCTTTAG[A/T]ACCCAATGTCTCTGC | 10451 |
rs537963901 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107825784 | TACTTGAATTTCTTC[C/G]TGCTTATTCAGGCCA | 10451 |
rs537964483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744219 | TACCATTAGTCCTTG[C/T]GTTTAAAAGATAAAC | 10451 |
rs537967438 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107603203 | ATTTGGATAATATAC[C/G]TGGAAGAGAACAGAG | 10451 |
rs537968849 | in-del | -/AAAG | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107841303 | AAGGGGGGGGTAGAA[-/AAAG]AAACAATTTTAAAAG | 10451 |
rs537982768 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107703079 | TGCCAACTATGGGAT[C/G]ATTTTACATTCTTCA | 10451 |
rs537987655 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107874113 | TTTCCTCCTTATTTG[C/T]TTATTTTCATAATGC | 10451 |
rs537998239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107833678 | TCAGGAATCAATTAT[A/G]CAGTGTGTTTATGAC | 10451 |
rs538003671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107770901 | TGTTTTTATAAAAAT[C/T]GTGAACAATGTAATG | 10451 |
rs538009489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888341 | AGATCAGCAAAACAC[A/G]TAGCGCTAGACTAGG | 10451 |
rs538031648 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107711976 | CAGGTGTGAGCCACC[A/G]TGCCCGACAACGCAT | 10451 |
rs538036284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107873607 | GCCACAGACAAATGC[A/G]CTCCCATTTCCTTAC | 10451 |
rs538043828 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107684210 | AATCTATGAAAATGC[A/G]TGGCTACATATTTTA | 10451 |
rs538048068 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595214 | ATTGATCACTGTGAG[G/T]AAAACATATATTAAG | 10451 |
rs538048549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107874692 | GGAAAGTTGATGCTA[A/G]TTTTTTGGTGTTGTT | 10451 |
rs538049101 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107708769 | GAACTTCAAAATCAC[A/G]ATGAATTTTTCCCTC | 10451 |
rs538067485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107931730 | TGGTCTGCTCAAAAT[C/T]ACACAGCCATTATTA | 10451 |
rs538068547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107867355 | TGTGTTTGCATGGCT[C/T]GGGTACTAAAGTTCT | 10451 |
rs538070153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959037 | GAGGCCAAGGCGGCC[C/T]GATGACCTGAGGTCT | 10451 |
rs538077770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107611230 | GCATTTCAGATGTCA[A/G]ATTTTCAAATGAGGA | 10451 |
rs538080277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107601941 | AGAACCATGGTAGAG[A/G]TCACTTAAAATAGCA | 10451 |
rs538083367 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107841326 | AATTTTAAAAGTATA[A/T]ATGGTATATCAGCTG | 10451 |
rs538090194 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107573678 | CAGGATGAAAAGACA[A/G]AGGTACTATGTCCCA | 10451 |
rs538092122 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107938397 | TCAAGGGAGGAAACT[A/G]TCAGGACCACAGGGG | 10451 |
rs538107328 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV3 | GRCh38.p7 | 1:107681799 | GCTGGGACTACAGGC[A/G]CCCGCCACCACCCCC | 10451 |
rs538109026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654873 | AATAATGAAATAGTA[A/C]CTACATTCTAAAAGT | 10451 |
rs538112194 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594486 | TCAAGTTGTCAGAAT[C/T]TCTTAAAAAGACTGG | 10451 |
rs538113084 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107708265 | AAGCGTGGATATAGT[A/G]GGACCAATCATGGGG | 10451 |
rs538120228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625652 | TCAGTGTGAAGCGGT[C/T]TATTTTCCGAAGCAC | 10451 |
rs538146760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107676013 | GGATCCTACAAATGG[A/G]AAAAGGACAAGGTAG | 10451 |
rs538147067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797825 | TCAAACCTTATCCTG[A/C]ACCAATACCACCTGG | 10451 |
rs538157184 | in-del | -/A | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107868016 | TAGTATGGGGTTGAG[-/A]AAGGGCTGAAAATAC | 10451 |
rs538162816 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107868786 | AAACCTGAAATCATT[G/T]AACTGGTGAAACACA | 10451 |
rs538164386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107884647 | TAGAGATGAGGTCTC[A/G]CTATGTTTCCCAGTC | 10451 |
rs538171285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832301 | TCTAAATATAATGCC[A/G]GAGGAAGCATATAGA | 10451 |
rs538183134 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572887 | CTCCAATTTTTCGTC[A/G]TGCTGGGAAAAGGAA | 10451 |
rs538184198 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733765 | CAAATCTAAATTTGA[C/T]TGGTGTACCTGAAAG | 10451 |
rs538185817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107754669 | GGCTGTGTTATGTAA[C/T]TGCCCTGCCCATTCC | 10451 |
rs538191067 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107788830 | TGTAATCATATTTGC[A/T]AATCCTTCTCTGCCT | 10451 |
rs538195956 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965390 | CCGGCGTCCTGGGGT[C/G]TTCTCTCGGGGCGGC | 10451 |
rs538200708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107894104 | ATCCCTCAAAAGCAT[C/T]CTTGTAAATAGTTAA | 10451 |
rs538204216 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107697145 | AGGGTGAGGAGAAGA[A/T]GCCATGGCTTCCAGC | 10451 |
rs538205449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107901976 | TGAACCCAGGAGGCG[A/G]AGGTTGCAGTTAGCC | 10451 |
rs538208952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825721 | CTCACAAAATATCTG[C/G]CTATCCAAATCTGTC | 10451 |
rs538212709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107764613 | CAGCTTCAAACTCTC[A/G]GGCTCAAGTGCATAC | 10451 |
rs538222818 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720881 | GCCTTTCTCAGTGGA[G/T]ACCAAAATGCAAGAA | 10451 |
rs538234410 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107657536 | TTAATCCTTTTTGAC[A/G]TTTTGTCCCGAGAGT | 10451 |
rs538247272 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107596100 | GAAGTCCTTGCTCAT[C/G]CATTAGCGCATCCAT | 10451 |
rs538267381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107696296 | TATCATTTCTTTGTG[C/T]TGGGAATATTCAAAA | 10451 |
rs538271666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786054 | CTGTGGGATGCTGTT[A/G]AAAAATGTCCTTAGC | 10451 |
rs538283507 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107863109 | TTCTCCTACATTAAT[C/T]TGAAACCCACTGTAA | 10451 |
rs538283521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804611 | TCTCAACAGGTTTCT[A/G]TAGCTATTATTCTTT | 10451 |
rs538291867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915219 | TATCACCATGAAAAA[C/T]TGTGGTAATGGGAAA | 10451 |
rs538301190 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588567 | ACCTACTAACTCTTT[C/T]AAGCCTCCTAACATG | 10451 |
rs538307944 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579678 | TGTTCTAAATACTGC[C/T]TCACAGCAGCTCACC | 10451 |
rs538321773 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107914179 | ACAGATGAATGTAAA[C/T]GGCTAATGAGTACAG | 10451 |
rs538325223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107930714 | ATTGATGAAAAGTCA[A/G]TGAAAAACTTTATAT | 10451 |
rs538340052 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107892703 | ATTCACTAAAAATTA[C/T]AGACATTCTAAAATT | 10451 |
rs538345496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107833583 | ATTTTTACTTATGTA[G/T]GTCTATACTTACCTA | 10451 |
rs538346641 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107587982 | AGAAATTCTAAGATC[A/G]TAAGTACTGCTCTGA | 10451 |
rs538355692 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107655556 | TGCTCCAGGACACTG[C/G]TTTGGGAAAAGGTTT | 10451 |
rs538360268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107647563 | ATCCAGAGGGAACTT[C/T]AAAACAAATAAATGT | 10451 |
rs538364409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107659150 | AAGGAAGGGATCCAG[C/T]TTCAGCTTTCTACAT | 10451 |
rs538364933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107908075 | GACAGAATTTTCAAC[A/G]TCATCCCTATACTTT | 10451 |
rs538370603 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107952398 | GAAATAATCTGCACA[A/G]TAAACCCCCATGACA | 10451 |
rs538379652 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107924153 | CAACCTCTTTCTTCT[C/T]TCCCGTTCCCTATAG | 10451 |
rs538382349 | in-del | -/AT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107796800 | TTTGTAAAAAAAAAA[-/AT]AAAAATATATATATA | 10451 |
rs538388542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702203 | GCAGGTACATCTTAC[A/G]TGGTGACAAGTGAGA | 10451 |
rs538389333 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689697 | TGCTAGCCCTGAAAT[C/T]AACCTTTACAAAGGA | 10451 |
rs538401827 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689127 | TTCTGGGGATAAGGG[C/T]GCACACGGCACTTGG | 10451 |
rs538402382 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107600299 | TTATAGTTATTTACT[A/T]AACTTGATAAAAGCA | 10451 |
rs538411526 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107749903 | ATAAAGTTTGTTCAT[A/G]AGCAATTATCTTTTT | 10451 |
rs538414376 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107887363 | GCAATATCAATAATA[A/C]TCTCATAAATAAATG | 10451 |
rs538459364 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107953756 | AGGCATAGGGAAGCA[A/C]GACGCTTGTTTATTC | 10451 |
rs538462648 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107747461 | CAATTCAAATTGTTT[A/G]ACTCCAAGTGACTTC | 10451 |
rs538466214 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107658201 | AGAACATGCGGTGTT[A/T]GGTTTTTTGTTCTTG | 10451 |
rs538478116 | snp | C/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107816627 | CTTAATGCTTGTCTC[C/T]TGACTCATTTATTTT | 10451 |
rs538480798 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107907132 | TTAGGAAGAAGCAAA[A/G]TACAAGTCAGAAAAG | 10451 |
rs538499406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107784243 | TGCTTTATTAAGTAA[C/T]GTATTCCTATTATAC | 10451 |
rs538509454 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572140 | GCTCCTCACAAAAAA[C/G]AGTGATGGCTGGGCA | 10451 |
rs538539102 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893431 | GCCCATTTTCATGCT[G/T]CTGATAAAGAAATAC | 10451 |
rs538540919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913945 | GATTACAGGCACCTG[C/T]CACCACGCCCAGCTA | 10451 |
rs538548009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107601140 | TTTTATGAAGAACCT[C/T]CTCTGGTCCAATTCT | 10451 |
rs538550600 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900985 | GAGACTCAGTAATAA[C/G]TGTGTCACCCACTTC | 10451 |
rs538577641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880613 | CCAGCCTGGCCAACA[C/T]GGCAAAACCTCATCT | 10451 |
rs538578224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893970 | GCATCATGATTCACC[A/G]TCAACACATCGGTTC | 10451 |
rs538582291 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107837679 | AGCATGGTACTGATA[C/T]AAAAAGTGACACATA | 10451 |
rs538612058 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107763236 | GAAGAAAGGACAGCA[A/G]GGGCACCTCACCCTG | 10451 |
rs538613344 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107681907 | CCTCGTGATCCGCCG[A/G]CCTTGACCTCCCAAA | 10451 |
rs538619057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603862 | CCAGGCTGGAGTGCA[C/T]GGCACCATCCCAGCT | 10451 |
rs538638638 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107632185 | TGTCAAAATTACCAT[G/T]GTCTCTTACCAATTA | 10451 |
rs538643575 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107922306 | TGTGTCAGTATCCAG[-/A]AAAAAAAAAATCACT | 10451 |
rs538646737 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107873086 | GTAGGTTCAAGTTCT[A/C]AACCACAATCTCATG | 10451 |
rs538647205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868062 | ATCAGAGCACTAAAG[C/T]TGTCCCAGGAACCAC | 10451 |
rs538659346 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107851604 | GAGCTCTTTAAATAC[A/C]CAGGAAGTCAAAGGG | 10451 |
rs538660210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107952283 | ATGGGCACACGGAGG[A/G]GAACCACACACACTG | 10451 |
rs538661959 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107732299 | CCCAGCGTGACTGAC[A/G]CAGAAGACGGGTGAT | 10451 |
rs538665859 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655964 | ACAAACACCAGTGAG[A/G]GTGTGGAGAAAGGGG | 10451 |
rs538705705 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107725818 | GTGCCCAGATGGCAA[A/T]TTTCAGTAGCTAACC | 10451 |
rs538715648 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107737038 | CAGAATAGAGGCCTC[A/G]GAAATAACACCACAC | 10451 |
rs538718216 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107731639 | AATCTTCTTCATTAT[A/G]AGGAAGAATCTTCTA | 10451 |
rs538720736 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662455 | TAATGTCACAGGGAT[A/C/G]TAAGTTATCTCTCTC | 10451 |
rs538752938 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832944 | GTGCTTGGAATTTTC[A/C]CTATCAAAAGTTTTA | 10451 |
rs538765897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107840762 | GGAGAAAGCACTGAA[A/G]GCATTTTAAAAATAA | 10451 |
rs538768987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107873812 | CTGAGAAGGCTGGTG[C/T]CTTCTAGATCACAAA | 10451 |
rs538779623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107610291 | AACTAAAGTGAAAAC[A/G]TTATTAAGAAAACCG | 10451 |
rs538793159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107848230 | AGGCAGGAGAATGGC[A/G]TGAACCCTGGAGGCG | 10451 |
rs538809826 | snp | A/G | 0.000100052 | 0.00707219 | synonymous-codon, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964723 | GGAGTGCGCCCGGAG[A/G]TTGTTAAGCAGCTGG | 10451 |
rs538809835 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832070 | AAATGCAATCATCCA[A/G]GTGTGAAGTAAAGTC | 10451 |
rs538835169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707491 | TTGGCTACAATTTAT[C/G]AAGTGCTGATTCCAA | 10451 |
rs538856431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872993 | ATTCTTTAACTTTCA[A/G]TGTTTTCTTTAGATC | 10451 |
rs538856863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107865436 | CTTGAATTGAGTCAC[C/T]GCAGACAAGGGACTA | 10451 |
rs538859773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107930129 | ATTTGCAAGCACAAC[A/G]GGGTGACTGTAGTAA | 10451 |
rs538868789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625094 | AAACACAGAGCACGA[C/T]CTAAGGATTTCCAAT | 10451 |
rs538869734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107938329 | GAGGAGGAAGGAGCC[A/G]CCAGATGGGACCAAG | 10451 |
rs538879694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107617457 | TCTTCCAGAAAATAT[C/T]AATAAAATTAATAAC | 10451 |
rs538880419 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107848824 | GTATATTTAGAAAAT[A/T]CCATCGTCTCAGTCC | 10451 |
rs538881214 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107759977 | AAATGTTTTAATGCA[-/T]TTTTAAGGAATAATC | 10451 |
rs538886302 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736176 | TTCATACTGAAAACT[C/G]TCAATAAACTAGGTA | 10451 |
rs538888242 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107886200 | AACTTACAATATTGA[C/T]ATATGTCCCAGGTAT | 10451 |
rs538888806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797155 | GTAGGAATTATGTCA[A/G]TTTTATATAGTAAAA | 10451 |
rs538894697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107653844 | ATATTTACCTATGAA[C/T]ATACATTAACTGAAA | 10451 |
rs538896904 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107609404 | AGCTACTAGTGTCAA[C/G]CAGAAGCAGTGGCTC | 10451 |
rs538905641 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107579432 | CAAAGTCCCATGTTT[-/C]CCCCCTGCAAGAACT | 10451 |
rs538907699 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720241 | ATAAAAAATTAGCCA[C/T]GTATGGTGGCACATG | 10451 |
rs538917896 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107749279 | ATCATTAGGGCATTA[C/G]AAATGATCAGATCTG | 10451 |
rs538928820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107706513 | AATGTTCCACTGCAC[A/G]CTGAGAATTATGGAC | 10451 |
rs538954535 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756277 | CCTGTTTTCTGAGCT[C/G]TTTTTCTTTTTTCTC | 10451 |
rs538962168 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107740065 | GCCAAGATGTGCGGA[A/T]CACCTGAGGTCAGAA | 10451 |
rs538963380 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107660159 | TTTATTCTCACTTGT[G/T]CCAGTTTCAGGTCAT | 10451 |
rs538968295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107616595 | ACCTAAAATAAAAGT[C/T]AAACAAATGTGATAT | 10451 |
rs538975648 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107928975 | TCAAACTCCCAAAAA[G/T]CAAAGATAAAGAAAG | 10451 |
rs538977596 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107748171 | AGAATTTGTCAACAA[A/C]TGGTATATAATCTTA | 10451 |
rs538981134 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107900534 | ATACCATATCAGACC[A/C]ATATTCAATCCACTA | 10451 |
rs538996351 | snp | A/G | | | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688539 | GTAATATATTTCCAC[A/G]GTCCCTCAGGCTGGG | 10451 |
rs539009801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579016 | ACTATTCCTGAAGGA[A/G]TAAGGGTAATACTTG | 10451 |
rs539019285 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594655 | GAGCATTAAATACTT[C/T]ATTAAACATGAGACA | 10451 |
rs539021390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719754 | ACTATAAAGACACAT[A/G]AACACATATGTTTAT | 10451 |
rs539023300 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107954423 | TTCCTTAGTTTTCCT[C/G]ATTTCCTTTCCTTTT | 10451 |
rs539047331 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107737386 | AAAGAGCTTCTGCAC[A/G]GCAAAAGAAACTGCC | 10451 |
rs539072942 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107856608 | TAACTAATTGATAGC[A/C]CTTTATTTTGTTCTC | 10451 |
rs539074742 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107810109 | ACTGATTAGAATTCT[A/G]CTGATAAATTGCCAC | 10451 |
rs539078843 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621842 | TCATCTGATATACCA[C/T]ACGGTGCTATCTTTA | 10451 |
rs539081318 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107638707 | TGACATGCAAAGGAC[A/C]AAGGAAACCCAAAAC | 10451 |
rs539083060 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107598264 | GGGAGGCTGAGGCAG[G/T]ACAATCACTTGAACC | 10451 |
rs539092919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635862 | CGGAATTCCTATGTC[C/T]GAATAACAGCTCTGC | 10451 |
rs539101350 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107627237 | TTCCTTCCCCATCTC[C/T]ATCACTCTCTGTGAG | 10451 |
rs539105110 | snp | A/C | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590445 | GCACCAGAAGAAATT[A/C]AGCCTATATACAAAT | 10451 |
rs539106828 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107643104 | TTTTCATCAACTCTA[A/T]CCTTTCTGCCTATTA | 10451 |
rs539106934 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107635173 | GACACATGCACATGT[A/G]TGTTTATTGCATCAC | 10451 |
rs539107651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595094 | GAGAATCTAAAATAA[C/T]CAGGTAATCTTGGGC | 10451 |
rs539116590 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923475 | GGCCTGTATTAGTCC[A/G]TTCTCACACTGCTAT | 10451 |
rs539124759 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107924563 | CCACCACCAAAAATA[C/T]CTATGGCTTTAGAAT | 10451 |
rs539140756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107678068 | CAAGAAGATCAACTG[C/T]CCTAGTGCAAAACTA | 10451 |
rs539141736 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107618978 | GGTCTCACTTTCGGA[A/G]TTGAGAATATCACAA | 10451 |
rs539145965 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594663 | AATACTTCATTAAAC[A/C]TGAGACATAATTTTA | 10451 |
rs539147153 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107731120 | CAGACTCTAAATACT[C/T]TTAACATTAAAGTAT | 10451 |
rs539153522 | snp | C/T | 1.81424e-05 | 0.00301179 | utr-variant-5-prime, intron-variant | VAV3 | GRCh38.p7 | 1:107688448 | GTCAGTGTAAAGTTA[C/T]TTTGTTTGGTTAGCA | 10451 |
rs539153585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107958363 | GCTAAAACTAAATCA[C/T]AGTTTTTAAAAACAA | 10451 |
rs539153829 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107815963 | GTTCTCGTAAGGAGT[A/G]CACAACCTACATCCC | 10451 |
rs539164279 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107606147 | GTAACACTCTAAAGT[A/C]CCACATCTATGAAAA | 10451 |
rs539168851 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107642558 | GAATTCCTTCTTGGG[A/C/T]AAGATTTAAGAACCC | 10451 |
rs539180846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728446 | TAGTGGCATTTGAGG[A/G]AAAAATAATCTGTTA | 10451 |
rs539183246 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107650500 | CGTAATTCCCAACAT[C/G]ATGGTATTAGGAGGT | 10451 |
rs539189485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107955522 | GATAAGGAAAAAAAA[A/C]TGCAAAACAGCAAGA | 10451 |
rs539201361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107684864 | TAAAGAAAAAATCTT[C/T]TCTGTCTGAAATTTT | 10451 |
rs539207697 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107760997 | TTTCCTTAACAATCC[C/T]TCTCTGTAAATAACA | 10451 |
rs539209535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819990 | ATGGAGAAAAGTGAA[C/T]CCTCATACACTGTTG | 10451 |
rs539227689 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694839 | GGTATGGTTCCTATC[A/G]TTGAGAGGGCTGCAG | 10451 |
rs539234303 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783614 | GACATGTACCATCCT[C/G]AACCCAGTGAGGCCA | 10451 |
rs539235504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107869485 | ACACTCTGTTAAGCA[C/T]TTGACATACACAATT | 10451 |
rs539236468 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965343 | GGGGATCCCGCGCCC[C/T]CGCCTGCAGCCTTGC | 10451 |
rs539239764 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107701107 | AAATGTCTTCTTTTG[A/C]GAAGTGTCTGTTCAT | 10451 |
rs539241091 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107670379 | CACTCTACTTCTATA[A/C]CCTATGCCTGGGCAT | 10451 |
rs539243153 | in-del | -/TGTTA | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107944496 | ATAACCTGAATTCTT[-/TGTTA]TATGTTCAGTGCCTA | 10451 |
rs539245060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698177 | GTAAAGTACAAATGG[C/T]CCCCAATTTTGGATG | 10451 |
rs539263516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862772 | AGGAATTAGAATACG[A/T]GCATTAGTGAGCATA | 10451 |
rs539288298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107920807 | GCACATTTTCCCTTA[C/T]GATTATTTGTGTGTG | 10451 |
rs539292914 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107623176 | AGCTTGTTCTATTTC[C/T]AGCTCTGCTATAAAA | 10451 |
rs539300795 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107790243 | GGCCTTATGTGCTTC[A/C]CATTTCCCCACTGCC | 10451 |
rs539306692 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107700649 | ATTCCTCTTTATGTC[A/G]GCATGGTATTCTATG | 10451 |
rs539324174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107924436 | AATTTAAAAGAAATA[A/G]CTGGTTTTCTGGGTG | 10451 |
rs539324830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659452 | TCCTATAGACTTCAG[C/T]TCTTCACAATGTCCA | 10451 |
rs539340928 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107608915 | TACCAATAAATTAAA[A/C]ATAGATTCAGTCTTT | 10451 |
rs539348450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107920128 | TTTCTTTCCAGAACA[C/T]AGTGTGTGAAAACTT | 10451 |
rs539352569 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667219 | CAAAGAGCCAGACAC[G/T]GTGCTAATGTTCCAC | 10451 |
rs539354459 | in-del | -/ATATGTTAC | 0.0154538 | 0.0865337 | intron-variant | VAV3 | GRCh38.p7 | 1:107925903 | TAACATATATGATAT[-/ATATGTTAC]ATATGTTACATATAT | 10451 |
rs539366411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738035 | GCAGCCATAAAAAAG[A/G]ATGAGTTCATGTCCT | 10451 |
rs539366589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613348 | TATTCTCTCCTTCTA[C/T]TAAATGTATTTGTAT | 10451 |
rs539374964 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107835226 | ATGCACACCGCACAG[A/G]TTCCATTACCCAGCC | 10451 |
rs539386135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107678950 | TATGTACATTTATAT[A/G]CATGCATTTATGCAA | 10451 |
rs539416670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107584931 | CATGTATTATATTGC[C/T]AATGTGCCAAAGACT | 10451 |
rs539422658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717437 | ATTCTGGTACGTTGT[A/G]TCTTTGTTCTCATTG | 10451 |
rs539460370 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107716709 | TTTTTTTGTTGTTGT[C/T]GTGTCTCTGCCAGGC | 10451 |
rs539462013 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107647607 | AATTTTCAGAAATTT[C/T]CCTTTCATAATTCTT | 10451 |
rs539481697 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107876744 | CTAACTGCAGTGGCA[C/T]ATATTTTTTTAAAAA | 10451 |
rs539482761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107932944 | AACCTTTGGCCTCCA[A/G]AGCTGTTAAAATACT | 10451 |
rs539488124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107811332 | ACCACCAGATCTGCA[A/C]AGGGTAAGATACTGG | 10451 |
rs539489279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619649 | AATAAGTCTATTTTG[C/T]GAGGAAAGGCCAAAG | 10451 |
rs539502766 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107583889 | AATGACTTTCTTCAC[A/T]GAATTGGAAAAAACT | 10451 |
rs539505527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946829 | GATCCCTCAACTACC[C/T]AAGGGAAATAGACAT | 10451 |
rs539506363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591619 | CCAATTCTTCAGATA[G/T]AGCCAGCAAATGGGA | 10451 |
rs539511203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107847030 | ATTGGAAGTAAAACA[C/T]TCCTCAGCAAATGTA | 10451 |
rs539513363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107799424 | TTCATATCCATATTT[A/G]TAAGAATGGTAACTT | 10451 |
rs539521724 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716341 | CTTTTAAAAGTGCTT[G/T]GGTGGGCCAGGTGTG | 10451 |
rs539523916 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107868251 | ACGTGTTTTATGTCA[A/G]ACAAGTACCTAAAAA | 10451 |
rs539526272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618979 | GTCTCACTTTCGGAG[C/T]TGAGAATATCACAAG | 10451 |
rs539542677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751415 | ATGTCAAGGACATCA[A/G]TTGATTTTAATTAGT | 10451 |
rs539553173 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107813228 | AATCAGTAAGTAAGT[C/G]TGGAAAGGCATGGGG | 10451 |
rs539568312 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107735854 | CCCTAACTCATTTTA[G/T]GAGGTCAGCATCATC | 10451 |
rs539570269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773646 | GGGAGGGAGGAGGAA[A/G]GAAGAGGAAGGAGCT | 10451 |
rs539582615 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107901150 | TTTACACCAGCTGGG[A/G]AGCTGCTATGTCCCA | 10451 |
rs539587681 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693041 | TGGGATTAGACCTTC[A/G]CGGTGGTGTACTGTG | 10451 |
rs539593473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107582941 | CCAGTAATGGGATGG[C/G]TGGGTCAAATGGTAT | 10451 |
rs539596729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107573879 | TCAAATATTTTCAGC[A/G]AGTCCCTGGTATCAG | 10451 |
rs539609043 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107598019 | AGTTTGTGCTCTTAA[C/G]TGTATCATACTATTA | 10451 |
rs539611892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625962 | TAATGGAAGAAAAAG[C/G]ACCACAACAGAATTT | 10451 |
rs539612714 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107937243 | ACCACCATGACTATT[C/G]AGATGTTACTTCTTA | 10451 |
rs539631309 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590288 | ACTTAGCACTCTAAT[A/G]TCTGCTGTGTCTCCT | 10451 |
rs539633327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107947981 | ATGAATACTCATACC[A/G]TTGGGAATTTGGGAC | 10451 |
rs539638065 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107953685 | GAACCCAGGTCTCCT[C/G]ACTCCTGACCTTAAG | 10451 |
rs539639972 | in-del | -/TGA | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107711180 | GAAGATATTTAAAAG[-/TGA]TAAAACTAATGAGAG | 10451 |
rs539648276 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107605953 | TACCTGTTAATTTTC[C/T]CTGGAGCCTTTTCTT | 10451 |
rs539656362 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107649568 | CCCCTTGGCTTTTTT[G/T]TTGTTGTTGTTAACC | 10451 |
rs539663089 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690966 | TTTTATTTAATCATG[A/T]TTCATGGTAGGATTC | 10451 |
rs539663844 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698290 | GATATTTTCCCGGGC[A/G]AGCAACATGCCCAAT | 10451 |
rs539665331 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107683220 | GGGTGCTGGATATGT[A/G]AGCATTAACCAGGCA | 10451 |
rs539667715 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107854273 | CGAGATTGTACCACT[A/G]CATTCCAACTTGGGC | 10451 |
rs539693224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917399 | TAGGAATTTTATAGA[C/T]AAGGGAACTAAGATT | 10451 |
rs539693585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107721168 | GACTGAATCAGGGCA[C/T]GAGAAAACGTGAAGT | 10451 |
rs539694796 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720744 | CAGGTTATGAAGATA[C/T]GTATCCTCTACGAGC | 10451 |
rs539694984 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107909882 | AATATTTTCTTTCAA[A/C]TATCAAGCTTGCTCA | 10451 |
rs539696953 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787505 | AAAGGCATCTTTAAA[A/G]GAGGTGATCCTAGTC | 10451 |
rs539699092 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107867505 | CTAATGATCTGGGAA[C/T]TGTGTTAACAGCCAG | 10451 |
rs539718113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589570 | GAGAGTAAACTTCTG[C/T]TGTTTTAAGCCACTT | 10451 |
rs539725725 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107880141 | AGTTTGGCAAGTGCA[A/G]TGAAGAATACATTCA | 10451 |
rs539726253 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107915869 | AAGAAAACAGAAAGA[A/G]CTCCTGCCCTCATGA | 10451 |
rs539727022 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107925477 | ATGGTGTATACATAC[A/G]ATGGACTATTATTCA | 10451 |
rs539746662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588852 | TTTCAGAATTCTTAG[A/G]TTCTCTTATTCCATA | 10451 |
rs539751274 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107686337 | AAAAAATTCACAATC[A/G]TAACTATTGAAAGGG | 10451 |
rs539752044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664086 | TTTCTTTTTTTCTTC[C/T]CTTTCTTAATGGTTT | 10451 |
rs539755916 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107916883 | TCAGGGGCCACAAAT[G/T]ATGGTTAGGGAAAAC | 10451 |
rs539766507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732707 | GTAAACAAAGTGGCC[A/G]GGAAGCTCGACCTGG | 10451 |
rs539774103 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751720 | GTCCAGGCTGGCTTT[C/T]TTGAGCTAGGACCTC | 10451 |
rs539778260 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107698065 | AACAAGAAACTTAGA[C/T]AGATTGCATATTTCT | 10451 |
rs539787265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690593 | ATCCCTCCTTTATTT[C/T]CTCCCTTGTCATTGT | 10451 |
rs539787419 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107882057 | AAAAAATAAACACCG[A/G]CTTCTCCAAAGTTGC | 10451 |
rs539793452 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689453 | AGATTGCTTTACACA[A/G]GAAGATTGCCTGGGG | 10451 |
rs539801343 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107670130 | AAATTGTCCAAAGAT[G/T]TGCACAGCAGCTTGG | 10451 |
rs539803046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677311 | CATCAAATATTGTTA[C/T]ACAAAGTCAATATGT | 10451 |
rs539810980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794083 | TTTCATTCTGTTCCA[C/G]ACGGGACCAAAGATA | 10451 |
rs539814336 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107671298 | GGACATCCAGAAGCA[C/T]GTTCTGTGAACAGAT | 10451 |
rs539815567 | snp | C/T | 1.79429e-05 | 0.00299518 | intron-variant | VAV3 | GRCh38.p7 | 1:107751082 | TTTTCTGACACTAAT[C/T]ACTTATTTTGAAAAT | 10451 |
rs539827472 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107573984 | CTGGTGCCACAATGG[A/G]TGCAAACAACTGCTC | 10451 |
rs539830300 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107709117 | CACTTTATGTAACAT[A/C/G]TGATGCCGAGTTAAG | 10451 |
rs539840222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786897 | ATCATGTTTTATTCA[A/G]TGGTTATTATTTTGT | 10451 |
rs539847966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107765778 | AGGTCAGTTGGTTTA[C/T]TGCTTCTCTTAACTC | 10451 |
rs539851583 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107814784 | CAGTGCTTATGGAAG[-/A]ATATTCTAGCAGCAA | 10451 |
rs539868760 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107793673 | GAGGTAGACAGTTTT[A/C]AACACCAGGCTAAGG | 10451 |
rs539871362 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939556 | CATTTTTTGGATATA[C/G]TGTTTTTTGGTTTTC | 10451 |
rs539884193 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107574299 | ATCAAATGCACAGTC[A/C/G]TGATTTCATTACAGA | 10451 |
rs539884884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895742 | AGCATTTTTATTAAA[C/T]AGTAATCCCACCCCA | 10451 |
rs539900179 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107626584 | TACTCAAGGGATGGG[G/T]TTAATAAATCAGTGG | 10451 |
rs539922619 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107902225 | CTAGACCAAGGGTCT[C/G]TACAGACTTTGCCTA | 10451 |
rs539924938 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107670653 | TTCTCTTTAGGTGGG[A/G]AAAGCAGTTACATAA | 10451 |
rs539937676 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107844175 | CCACCGAGGGCAAGC[A/G]GAAGCAGGGTGGGGC | 10451 |
rs539946827 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857087 | AAGTTTTCCTCATGG[A/G]TGTGTCTGTGAGGGT | 10451 |
rs539958937 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107895151 | CTATGGGAAGCAGGA[A/G]CAGGAACACAGGGCT | 10451 |
rs539966757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677119 | TATGCTGAAAGATAA[C/T]TAATTGCCAATATGA | 10451 |
rs539967744 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107758435 | AAATTAGCTGGGCAA[C/G]GTGGCATGAGCCTGT | 10451 |
rs539967797 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107812112 | AATGTTTAAATAATA[C/T]CATTAACAAAAGTTT | 10451 |
rs539971632 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710929 | GGGATAGTTTCTTAC[C/T]ATGATAAAGAATATC | 10451 |
rs539976282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107764998 | ATGGGAAATGTACTG[C/T]TTCACTGATCATAAA | 10451 |
rs539978033 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107686205 | CCAGAGGAACTTTCC[A/G]AAGGTCCACTCCAGA | 10451 |
rs539979019 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107683802 | TGCCAACTCCAAATA[C/T]TGGGACTCAATTTGT | 10451 |
rs539981666 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107869813 | TTTTCACACTTTCCC[C/T]TGAGTCCCAAGTCCA | 10451 |
rs539997732 | snp | A/C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107746462 | TCAAAGATTAAGAAA[A/C/T]CCAGGTTCTGTGCAT | 10451 |
rs540002363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107853964 | TGTAGGGTAACTGTA[C/T]TTTTTTTTTCTAAGT | 10451 |
rs540005621 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107757830 | CTTAGAAAGTTATTG[C/T]TCCTTAAGTTTTCAC | 10451 |
rs540007405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107634499 | AAGACTTACATGTTA[A/G]ACCTAAAACCATAAA | 10451 |
rs540009422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107853795 | TAATTTGACAATGTC[C/T]TTAAGTAAACCAAGA | 10451 |
rs540011834 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107783596 | TGTGTCTTCTACATG[A/G]TGGACATGTACCATC | 10451 |
rs540022431 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107861797 | CTCAGAAGCAGCAAG[C/T]AGCATCCTTCATTTC | 10451 |
rs540023187 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107615665 | AGTAAACAGGCAACA[C/T]AGAGAATGGGAGACA | 10451 |
rs540025877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771921 | ACTTGCGTTATATTC[C/T]TCAAACACAGGCAGG | 10451 |
rs540036173 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107758707 | CCTGTCTCTACCCTA[C/T]TCAGACTTCTGTGAT | 10451 |
rs540048997 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107785401 | CCCAAAAGGAAAGGC[C/T]GGGTTCAGTAACAAC | 10451 |
rs540051208 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771401 | GTGACTACAGGTGCC[C/T]GCCGCCACGCCCAGC | 10451 |
rs540054291 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589134 | AAATTAGAATAAGGA[C/T]GGAAAATTTTAGAGA | 10451 |
rs540058499 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690040 | AGTTTTCCATCCAAG[A/G]AGATTGAGGAAAGCT | 10451 |
rs540063908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107805220 | CAAGTTTTGAAAAGT[C/T]GTCTACTGTTTCTTT | 10451 |
rs540074080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107727277 | TCTCCTTGACCAGCA[C/T]TTTTTAAGCTCCACT | 10451 |
rs540081092 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107886003 | GGAAGTGGCTGAACT[A/G]AACATCCAAGGATGA | 10451 |
rs540082961 | snp | A/C | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588100 | GGATACTGGTTGCTA[A/C]CTTTTAAAGCCATCA | 10451 |
rs540084077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107641684 | CCAGGTATTACTGTG[C/G]GTAGGTAAAAAGCAA | 10451 |
rs540085736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107640684 | TTATATAAAGTTGCA[A/C]TAATGATCCAAGAAG | 10451 |
rs540099477 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107585671 | ACAATGAAACCTGCT[A/G]TGATGTCCTATAAAA | 10451 |
rs540099916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107908471 | TATCTTTTCCTGTTT[C/T]AGCTTAAAAAAGAAA | 10451 |
rs540106288 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819171 | GTCTTTAACAACATT[A/C]TATCTTTTCCCCTTC | 10451 |
rs540108547 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107908331 | TAGGGCTATAGGTGG[C/G]TGATATCATAGGTGG | 10451 |
rs540133451 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107647949 | ACAGCTTATAGGGCT[C/G]TTTCTAAGAAAGCAT | 10451 |
rs540141705 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107863765 | TTTAAAAAACTACCC[A/G]AAAGATTCACTGTTT | 10451 |
rs540146930 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902127 | AAAAAATTCAGAGAA[A/C]TATTAAGCATGCCTT | 10451 |
rs540157106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953144 | AATCTGGAATTAGGA[C/T]AGTTGGACTCAAGTC | 10451 |
rs540157185 | in-del | -/A | 0.00192738 | 0.0309835 | intron-variant | VAV3 | GRCh38.p7 | 1:107705072 | AGACCTAAAAAAAGG[-/A]AAAAAAATAACTTTC | 10451 |
rs540167183 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915406 | CCAGGTGCAAGTTAT[G/T]ACTATCACCCCCATG | 10451 |
rs540168025 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107867744 | TGCCAGGCTGAGCCA[C/G]CTCTAGGCTGGAAGC | 10451 |
rs540168073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107874791 | TGAAATTTAACTATA[C/T]AATGCAGATACATAA | 10451 |
rs540171328 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737187 | ATCCCTTCCTTACAC[C/T]TTATACAAAAATCAA | 10451 |
rs540177705 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107573477 | ACCCCAATTAAACTG[A/G]GGTTTTATGTCCATT | 10451 |
rs540182501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868527 | CTCAAGTAGGTTGTC[A/G]GGATGCCTGTGGTGA | 10451 |
rs540182817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107861171 | ACAGTATAGAAAAAA[A/G]GGAATATATGCTTTT | 10451 |
rs540185217 | snp | C/T | | | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107571121 | GGGAACCCTGACTAA[C/T]ACAGGGATCATTCAA | 10451 |
rs540186227 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107742883 | AGAGAATATAGAAAA[C/G]GTGGTATTACTCACT | 10451 |
rs540189188 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107758608 | AATGAGCTTCTGATC[A/G]GCCTTCTGACTTGCA | 10451 |
rs540202652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619272 | AGAAGATAGAAGACA[A/G]AATTTACAGAAACTA | 10451 |
rs540219853 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107846684 | AGACAAAAAAGGGCA[C/T]TACATAATGGTAAAG | 10451 |
rs540221616 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107880968 | AGAAAAGTTTTAATT[G/T]TTTTTTAAACACATA | 10451 |
rs540230759 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107853964 | TGTAGGGTAACTGTA[-/T]TTTTTTTTTCTAAGT | 10451 |
rs540238294 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107873227 | CAACTCTCCTACAAA[A/G]CTTCCGTTGTCTAAT | 10451 |
rs540242936 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107663501 | AAAATGAATATAATG[-/A]AAAAAAAATGGTTTG | 10451 |
rs540273169 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107936473 | TCTTACCGAGTTTTT[A/G]AAGATATGACAATCT | 10451 |
rs540273401 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107840128 | CAGAAAATAGAAAGA[A/T]TACTTCCTAAAGTTC | 10451 |
rs540274192 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618427 | TGAAATGTAAGTTTT[A/G]GATGATTTTCAGATT | 10451 |
rs540279404 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107634111 | TTCTTCACAGAATTG[A/G]AAAAAACTACTTTAA | 10451 |
rs540286228 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107675275 | TAATCTTCAGAGCAC[C/T]TAGTATGTGCTAAAC | 10451 |
rs540288061 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107845855 | TGACAGGGAGAATGG[A/C]ACCAAGTTCAAAACC | 10451 |
rs540290989 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721290 | ACTCATCCAAAGATA[C/T]TGGCTGCTACTGTAT | 10451 |
rs540297314 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107628228 | AAAGATCCCCCTAAT[C/T]AGCCCTTCATTTTTC | 10451 |
rs540297458 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107582492 | ATGTATACATGTGCC[A/T]CGCTGGTGCGCTGCA | 10451 |
rs540305961 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107909007 | AATTATATACTTTAC[A/C]TCCTGTTAAAGACAT | 10451 |
rs540308712 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107835220 | AAGAGCATGCACACC[A/G]CACAGGTTCCATTAC | 10451 |
rs540315052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107610732 | TAGAAAATGAACAAA[A/G]ACAAAGCAGGTATAT | 10451 |
rs540325928 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107601011 | CAGGTGAAAGCTCAA[A/G]CTGGTACGTCTTGCA | 10451 |
rs540331245 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107937793 | AATTATTAACACAAT[A/G]TAATGACTGCATTAA | 10451 |
rs540342737 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107641233 | TTGGGCATTCTTATA[A/T]AACAAGATGACAGAC | 10451 |
rs540352516 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107617741 | CTTAGAATTCCTTAT[A/G]TGTTATATCCAGTCC | 10451 |
rs540356992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107683431 | CAGCAATTCCCATAT[C/T]CTTTCATAAGCACTT | 10451 |
rs540358225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107661251 | ACCAGCCTCCTTCAC[A/G]GGGCAGCTCTGTGAC | 10451 |
rs540372687 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107854229 | ACATGAGAATCACTT[C/G]AACCTGGGAGGCAGA | 10451 |
rs540373110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862078 | CATTATAATTGGCAT[C/T]GAGGCAAACCAGAGA | 10451 |
rs540375936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945692 | CCAGGCGTGGTGGCG[A/G]GCACCTGTAATCCCA | 10451 |
rs540382154 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818674 | TAAATAATAACACAT[A/G]AATGTAAAACACACA | 10451 |
rs540389357 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753062 | GCAACCCAAATGTTC[A/G]TCAATGAAAAACAGT | 10451 |
rs540411023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107852149 | TTAAAATGGAACTAA[A/G]ACTGTACCTATACCT | 10451 |
rs540428334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107596873 | GAAGTATAGTACCTG[C/T]CATAGCTCCGCATAT | 10451 |
rs540433787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107623854 | GTTCAAAAGACAGTA[A/C]AAAATGTCCCTATCT | 10451 |
rs540435267 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756400 | GATAGATCCATAAAC[A/G]ACTTCTTTAAAATTT | 10451 |
rs540436260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107779068 | ATTATGATCTACTCT[A/G]TAGGAAATAAACATA | 10451 |
rs540438392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107960734 | CTTGGTATTCCCTCC[A/G]CCAGGAATATTCTTT | 10451 |
rs540442447 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107681956 | TGAGCCACTGCACCC[A/G]GCCACGTATGTTCTT | 10451 |
rs540448200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107852726 | TTAAGTATGTAAGAC[C/T]CTCTGAATATTTATT | 10451 |
rs540449770 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953448 | AGTAACTTTCCCAGG[G/T]TCAGTGTTGTTAAGT | 10451 |
rs540463067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841891 | TGATAATTGGGGTGC[A/G]TTGGGTTAAATAAAA | 10451 |
rs540470156 | snp | C/G | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107596233 | TGCCTGCTCTATTAC[C/G]CCTCTGTCCAGCTGA | 10451 |
rs540473373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786224 | AAATTATAGTTTGTG[C/T]TGTCCTTGGTAACAA | 10451 |
rs540475862 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107763367 | CTTTGACAATAACTC[G/T]GAAAGAAGGAAGAAC | 10451 |
rs540480270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107863962 | GAAGTGTATGTACAG[C/T]CAAGTTTTCTCTCTA | 10451 |
rs540494638 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107809518 | AAATATTTTATGAGC[A/G]TTTATAATGTGCAAA | 10451 |
rs540499109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107696601 | TTAGACTATGTTAAA[C/T]ATTATTGCTATAAAG | 10451 |
rs540502070 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966584 | GCCCAAATTTTTTAT[C/T]ACGAACCATGCTTTA | 10451 |
rs540505330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107922883 | CGTGAACCCGGGAGG[C/T]GGAGCTTGCAGTGAG | 10451 |
rs540513763 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107726040 | TAGACCAAAAAAAAA[A/T]TCTCTAATGAAAGAT | 10451 |
rs540517074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804210 | CCAGCCTATGTCTTT[G/T]AATTGGAGAACTGCA | 10451 |
rs540518144 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881528 | CTAGCCTCTCTCTCA[G/T]GTATATCCAGTGAAA | 10451 |
rs540525425 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107825936 | TAAATCCCTATCTAT[A/G]CAGTTAGGTTATAGG | 10451 |
rs540525496 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107817770 | CATCAGTCAGAGCTA[C/G/T]CATAAACCTATAGTT | 10451 |
rs540554004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603339 | TTTAATACGTCCAAA[C/T]ACAAATGCTCTACAA | 10451 |
rs540560880 | in-del | -/CGGCGGAGGGGGG | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965302 | GCGCGGGGGAGGGGC[-/CGGCGGAGGGGGG]CGGCGGCCAGAAAGG | 10451 |
rs540578122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107611344 | TACATTTTTAAAATC[A/T]CAACTTTGTAAAATC | 10451 |
rs540580605 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107730504 | CGTTGCATTAATCAT[A/G]TAAGGCTCAAAATCA | 10451 |
rs540587917 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107638954 | CACACGGCATATATA[C/G]ACATAAAGATATATA | 10451 |
rs540590992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107602683 | AACCAATATTTGAAG[C/T]GAGAAGGGAGGTTGG | 10451 |
rs540594942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662030 | AATTAAGCTGCTCTG[C/T]AAGCAAACAGAATTT | 10451 |
rs540609446 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107618530 | TGGTGCAAAAGTAAT[A/T]GTGGTTTTTATCATT | 10451 |
rs540660398 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107856524 | CTTTTCCCCCAGGAC[C/T]GAAATATTAAAAAAA | 10451 |
rs540664668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107708174 | AGATTTTATACAGGA[C/T]TGACATCACATTTAG | 10451 |
rs540665513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107931244 | ATGGCATTCTGACTA[C/T]TTAGGAAAATCTTTA | 10451 |
rs540667365 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107922387 | AAAAACTGAAAGTCT[A/G]TTATCTAACAGAAAT | 10451 |
rs540674685 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107715028 | ATTTAAAGTGGAAAA[G/T]ATGTCAGATTATCTG | 10451 |
rs540685390 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107953547 | TGTAAAACATTTTAG[G/T]TGCTATTTAGTATAT | 10451 |
rs540704445 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107791409 | AAAAGACTGCTGCAA[C/T]AGTTCAGGTGATAGA | 10451 |
rs540709389 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107669118 | GTGTTCTTTAAAATT[A/G]AAGACAGAAAAATTC | 10451 |
rs540718677 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107865662 | AGATGTTATTCTCTT[A/T]TAAACAACAGGGATC | 10451 |
rs540719963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746838 | GTAACCACTCTTAAG[A/G]AGAGAAGTCAAATGC | 10451 |
rs540730611 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107887212 | TAGCCATGAGGACTG[C/T]GCTCTTACCCGCATG | 10451 |
rs540741782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711629 | TCTAAGAAAAATCCT[A/G]ACATGAAAAGTTTAG | 10451 |
rs540747381 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107757165 | TATATGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 10451 |
rs540762332 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107883471 | AAAAATTAAATGCAA[C/T]GATTCCTTAGTAGTC | 10451 |
rs540763508 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107839636 | AGAGAAAGAACAACT[A/T]AAGCTTAGAGCAGAC | 10451 |
rs540772148 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107802037 | TGCCATCTCTTCATC[A/G]GCATTTTAAGGTTTA | 10451 |
rs540789749 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107675232 | AAATACAGGTATCTA[C/T]ATGTATCAATAACCA | 10451 |
rs540795454 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107621448 | GTTTCTTGGTGGATG[G/T]GTGTGGGATGTACGT | 10451 |
rs540799159 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753911 | TACACAGCTGTCCAA[C/G]AAATATGCTATGGAA | 10451 |
rs540801311 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107740553 | GGAGTTAAAAAACAT[C/T]TTGGAGCTAAATCAT | 10451 |
rs540804479 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107580091 | TAATTACTGTACGTT[C/G]TGTGTTGTATCCCCA | 10451 |
rs540806823 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107944434 | TTCTTCCACAGGTAA[A/T]CATGAGATACAGGGA | 10451 |
rs540810316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913974 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 10451 |
rs540811581 | snp | A/T | 0.216649 | 0.247765 | intron-variant | VAV3 | GRCh38.p7 | 1:107949317 | GTTTATTTTTGTTTG[A/T]TTGTTTGTTTTGAGA | 10451 |
rs540811896 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107848797 | TTGTCTCTGTTTGCA[A/G]ATGATATGATCGTAT | 10451 |
rs540843570 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107937012 | GGCCAATGTGACTAC[C/T]GAGATTGCCACACCT | 10451 |
rs540846999 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107681493 | AAGCAACTTTAAATA[C/T]ATAAGTCAAGCCTAA | 10451 |
rs540850509 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107832141 | GATGGCAAGGACTTG[A/G]CAGCCATGGGGACTG | 10451 |
rs540852093 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107941232 | TTCTAAATTTCCTAT[A/C]TTCTACTTCTTCTGA | 10451 |
rs540852898 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107674417 | CATTTTCAAAATTAA[C/T]AATGCATAAAATAAA | 10451 |
rs540852930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107681943 | GGGATTACAGGCGTG[A/G]GCCACTGCACCCAGC | 10451 |
rs540871593 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107901185 | TTGTAGCTGACAATT[C/T]ACCTATGTGATTAAA | 10451 |
rs540874295 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107628884 | TCCATTTACCCTCTT[A/C/T]ATGAAGACCTTGTGA | 10451 |
rs540875849 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107677541 | CACTCCATATCTGAC[A/G]TTCTAAGTAAGGAAC | 10451 |
rs540876149 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107639626 | GCAAATCAAAACTGC[A/C]ATGAGACACCACTAT | 10451 |
rs540883694 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107676462 | TCTGTGAGGTGCATG[C/T]TGACAAGAAGCCAAT | 10451 |
rs540887184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107723366 | CAAATTCACCTTCAG[C/G]GTTGTCTTCCCACAC | 10451 |
rs540892427 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588141 | AAAAATGCTTTAGAG[G/T]AGCTGGTAAAGATCC | 10451 |
rs540910921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719394 | CATCAAAAAGTGGTC[A/G]AAGGATATAAACAGA | 10451 |
rs540921285 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107731736 | ATCCAAGCACAGCAT[A/G]TACTTGGAAAGAAGT | 10451 |
rs540925707 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636145 | AGGAAGACACTGAAA[A/G]ACTTTAACAAGAAAT | 10451 |
rs540945217 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929180 | GTAGTCCCAGCTATT[C/T]GGGAGGCTGAGGCAG | 10451 |
rs540952481 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107722770 | CTTGGGCTTCTTTTT[A/G]AAGAGTGATGAAACA | 10451 |
rs540965796 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107762451 | TCATCAATTACTGCA[C/G]TTCATTAGAAGGATA | 10451 |
rs540969723 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107770286 | GCCACCAGCCCTCCC[C/T]CCCCATCACTCTCTA | 10451 |
rs540973010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948386 | GTCATTAGTGTTCTG[C/T]AATGAAAACCTGCAT | 10451 |
rs540974182 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107599625 | TGAATTTAATGACTA[A/G]GAAAGACAAAGATTC | 10451 |
rs540981193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107820873 | CCACTTTTTTAATGT[A/G]TAATAAGGGGCAAGT | 10451 |
rs540986496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107829364 | TCTCCTAGCTGCATT[C/T]TGTCAGCAAGCCATG | 10451 |
rs540991226 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728943 | CAGAAAATCCATTAG[C/G]TTGCTCTATGGTGTT | 10451 |
rs541007241 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107759536 | AAATAAATTTTACTC[C/T]ATAGAATTTTGAGAG | 10451 |
rs541010519 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107693368 | TATTAACAAAATAAA[C/T]TTAACACATCTTTTT | 10451 |
rs541021261 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782670 | CATCCGTTAACTCTA[A/C]GTTTAGCCAAAGCAA | 10451 |
rs541024338 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591249 | ATTTCCTTGCACTTA[C/T]GCTTCAGCTTCATAA | 10451 |
rs541025073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107836944 | AACAAAAAAAAACAG[A/G]TGGATTCACAGCCAA | 10451 |
rs541025962 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107585397 | AACTAGAATAATCCT[A/G]TTAAAACTTTAAAGA | 10451 |
rs541053370 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107789070 | AACTCCCTTTGAATG[C/G]ACATGCCCCATGTGC | 10451 |
rs541062888 | snp | G/T | 0 | 0 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590823 | CACTATGCAACTCAT[G/T]TTCAAAGCATGCTTA | 10451 |
rs541062978 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107598445 | TATGTGTTCATGATG[C/T]ACTAGGAACTTTGTT | 10451 |
rs541079700 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107752029 | AGGGATTCTGAATAG[C/T]CAAAACAATCTTGAA | 10451 |
rs541081661 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920296 | AATAGTTGAAAAGCT[A/G]GATAAAATGCATAGG | 10451 |
rs541095592 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107698501 | TAGGTGCATTGAATG[C/T]AGTTTTGACTTACGA | 10451 |
rs541095987 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917022 | GCTAGAAATGTTGGT[A/G]ACGATCAGATTGTCC | 10451 |
rs541102687 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107830901 | TTAATTTGTATATCG[G/T]GTTATATCTGTATTA | 10451 |
rs541113697 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107903889 | TTCTCTTGGTCACAC[A/C]CAATCCATCAGCAGC | 10451 |
rs541120380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107820274 | AATAGAGTACTATTC[A/G]TCCATAAAAAAATGA | 10451 |
rs541128827 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107794945 | GGGAAGAGTATTCAG[C/T]ATTGTTCTCTGACGG | 10451 |
rs541134234 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107691864 | GTTCAATGTGCATTA[C/T]TGGTGCAAGAGAAAC | 10451 |
rs541134856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917491 | TGACCCACCATACTC[C/T]TGGATCATAAAGGGG | 10451 |
rs541141348 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107806680 | CAAATGAGGTGTTGC[C/T]CAGTCCAACATTGTA | 10451 |
rs541145052 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107731965 | CCTAATTATTTGAAG[C/T]GAAAGCATATACACT | 10451 |
rs541164650 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107613393 | TTCTGTTTTATTTTT[A/C]ACTTCTTAATCTCTC | 10451 |
rs541169528 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107700955 | CTCCACTGCCTCAGC[A/C]GCATCTATTGTTTCT | 10451 |
rs541174807 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107657605 | TCATATCACTTTGGA[C/T]GTATTACTTCTGATC | 10451 |
rs541180603 | snp | C/G | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594922 | CAACTTTTATTATCT[C/G]TTGCTGCTGGGAAGG | 10451 |
rs541184127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672557 | TGTCTGTAACTTTGA[C/T]TCCTGGTAAATTTAA | 10451 |
rs541187243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107606210 | CTATGAATATTATTG[C/T]AATATTCATAGTTTG | 10451 |
rs541188658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753159 | TGACACATGACTACT[A/G]CAAGGATGAACTTTG | 10451 |
rs541190376 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107791384 | TTTTTTTGGTGATAT[-/C]AAAAAAAAAAAAAGA | 10451 |
rs541203158 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710947 | GATAAAGAATATCAA[A/G]CTAAAGATAATAGAA | 10451 |
rs541209149 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107930704 | AAATGACATGATTGA[C/T]GAAAAGTCAATGAAA | 10451 |
rs541210157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107961785 | ACTGGGATCCCATCC[A/G]TGCTTTTATTTTGAA | 10451 |
rs541249410 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107679296 | AGAGTCTAACAATGA[A/G]CATCTGAGAAACAAG | 10451 |
rs541254231 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107780386 | GATCTTCAGTACTTA[A/T]ATCTAAATGTTAAAT | 10451 |
rs541265265 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107794158 | ATCTCAAAGATCCAT[A/G]TGAGTAGGACATGCC | 10451 |
rs541268624 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107834700 | AACATACTTTGAACA[C/G/T]ATCTTTGGAGAGAAA | 10451 |
rs541282950 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107695835 | AAGTAAGGTAAGGCC[G/T]AAATGTGATGTGCCA | 10451 |
rs541290381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787123 | CCTATCAGAATACCA[C/T]GGCCCAGAAAAACTG | 10451 |
rs541293166 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902635 | TTTTAGAATAACCTG[A/G]GGTCCTACATGTTTA | 10451 |
rs541296041 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807575 | TTGTGCAATGTGCAC[A/G]TAGCAAATCCCTGTG | 10451 |
rs541300638 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793893 | AGTAAAGGAAGCAGA[C/T]AGGACAAGCATTATG | 10451 |
rs541302911 | in-del | -/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751674 | AGTACAGAAAGGGGC[-/G]GGGGGGGCGCGCGCT | 10451 |
rs541323925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107932543 | TGGTAGGCTGAATAA[C/T]AGCCTCCAAAGATGT | 10451 |
rs541327187 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107877661 | AGTCACTTATATACT[C/T]TCACTTTTCCAGGCA | 10451 |
rs541332493 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790142 | TCTAGAAGCCCATGG[C/G]CTCTTCAGTGGAACC | 10451 |
rs541337308 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107799691 | TAACTTTTCTTTATG[C/G]TGGGAATGTTCAAAT | 10451 |
rs541344275 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107888716 | CCCCCGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 10451 |
rs541366086 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107856128 | GGTGAGAAGCAAGAT[G/T]AGAGAAAAGCCTATG | 10451 |
rs541373516 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107792243 | TTTTTCTTACATTTT[C/G]CCAAAATAGAAACCT | 10451 |
rs541375330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767499 | GCAGTTTATTTAGTG[C/T]TAAACCTTCAGCTGA | 10451 |
rs541385927 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107883369 | TAAAGAATACATCTA[A/T]ATTGTCTTTGTATCC | 10451 |
rs541388543 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107885862 | AGACTGTCCCAAACT[A/G]GGGAGCTGGGAGCTA | 10451 |
rs541390375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657702 | GGATTCCATGCAAAG[A/G]TTGTAGCAAAATATT | 10451 |
rs541400432 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733974 | AGAAAGGTCAGGTTA[C/T]CCACAAAGGAAAGCC | 10451 |
rs541401397 | in-del | -/AAGG | 0.00517822 | 0.0506191 | intron-variant | VAV3 | GRCh38.p7 | 1:107651538 | AGGAAGAAACAAAGT[-/AAGG]AAGGGAGGGAGGGAG | 10451 |
rs541406241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107870456 | AGAATTGTCTATTCA[C/T]GTCCTTAGCCCACTT | 10451 |
rs541410988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107685019 | GCACAATAGAAGCTG[C/T]CTTTCTACTGATTTT | 10451 |
rs541414353 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107766765 | GGAGAGGACAGGGTA[A/G]AAGAGGAGGAGGGAG | 10451 |
rs541421067 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107692530 | CTCACGTAAAAGTAC[A/T]GTGATAAAATGCCTA | 10451 |
rs541448343 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107645999 | CTTCTCTCCATTGAC[C/T]TACTGCCTTCCATCT | 10451 |
rs541449160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773427 | CATCAGTTACTGCAG[C/T]GTTATAATCAGCATC | 10451 |
rs541449945 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107728622 | GTATATGTATATGTA[C/T]ATGTATATGTATATG | 10451 |
rs541509565 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107621350 | GCTTTAGCTATATAA[C/T]AACTTCTACTTATTA | 10451 |
rs541513159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107733964 | GCAGCCAGAGAGAAA[A/G]GTCAGGTTACCCACA | 10451 |
rs541522688 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921669 | CATCCAGAGGAAAAT[A/G]TTTTAAATGGAAATT | 10451 |
rs541531970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107794305 | TACCACCCATGGGCC[A/G]GTACTAATAAAACAG | 10451 |
rs541532480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649802 | CAGATCATTCATGCA[C/T]TGATATTGGCTTTGC | 10451 |
rs541549348 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107610652 | ACATAGAGCTTCGCA[C/T]AAGGAAAAATATTGC | 10451 |
rs541551357 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738766 | TTGATTATTATCATA[C/G]AATTCACTGCAGTGG | 10451 |
rs541565907 | in-del | -/A | 0.0103295 | 0.0711199 | intron-variant | VAV3 | GRCh38.p7 | 1:107666311 | TCTTACTCTTAAGGG[-/A]AAAAAATATAAGAGT | 10451 |
rs541571630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107869724 | TTATTTAGTGGTGAT[C/G]TGAGATTTTGGTGCA | 10451 |
rs541572049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107752148 | ATACAAACAGGTATA[C/T]AGACCAACAGAATAG | 10451 |
rs541572808 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107605417 | TCCCACTGCTTCCTC[A/G]CTTTGTGATATCTCC | 10451 |
rs541582784 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657191 | AACTCCTGACCTCAA[G/T]TGATCCGCCCGTCTC | 10451 |
rs541591759 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107745163 | TGTTTCACATATGAC[C/T]AAATGGAATTGTGAG | 10451 |
rs541591805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738136 | CGCATGTTCTCACTC[A/G]TAGGTGGGAATTGAA | 10451 |
rs541596283 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875746 | TGGCCTGTTGTGCTG[A/C]ATATAGAGTGAAAGG | 10451 |
rs541596471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107628100 | CAACCCAGTATTGTG[C/T]CTTGATGATAAGGAA | 10451 |
rs541606003 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107760286 | AAGACTAACCGTGGA[A/C]ACCATAGCTTTGTGG | 10451 |
rs541639378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107856038 | GAAGCACAGCTGGGC[A/G]TGTTCTGAGTAGGAG | 10451 |
rs541639702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107848190 | TGGTGGCAGGTGCCT[A/G]TAGTCCCAGCTAATT | 10451 |
rs541656345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612953 | AAACTCATCCTAGTG[C/T]CATTCCTTTTTCCAA | 10451 |
rs541661316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940275 | CTCCACTTTTAAAGA[A/G]ACCAAAGAATTATAA | 10451 |
rs541663948 | snp | G/T | 0.0486741 | 0.148216 | intron-variant | VAV3 | GRCh38.p7 | 1:107635185 | TGTATGTTTATTGCA[G/T]CACTATTCACAATAG | 10451 |
rs541670800 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940095 | CATCCTCTCAAATTT[C/G]GTATTCTATATTACC | 10451 |
rs541699150 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896860 | AGTTAGTTTACAATG[G/T]ATCACATGTGGGACT | 10451 |
rs541709768 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107832443 | CTTTAACAGTCTGAA[A/C]AATGACCTGCGAGTC | 10451 |
rs541714735 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107764027 | CTGATACAACAAACA[C/T]TGTTCAAAAGTTCTT | 10451 |
rs541722530 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107727902 | CATTATAATTGAATA[C/T]GGAATTGCAAGCTGG | 10451 |
rs541727648 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619837 | GTGACATTTTGTGAC[A/C]GTGTATGTTGGCCAA | 10451 |
rs541729749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591099 | CTTCACACAAACGAC[A/C]TCTTTGCTATGCAGG | 10451 |
rs541734304 | in-del | -/G | 0.0287284 | 0.116357 | intron-variant | VAV3 | GRCh38.p7 | 1:107844386 | TTCAAGCACAAAACT[-/G]GGTGGCCATTTGGGC | 10451 |
rs541759285 | in-del | -/AA | 0.211819 | 0.247067 | intron-variant | VAV3 | GRCh38.p7 | 1:107724836 | GGATGTGGTGGGGGG[-/AA]AAAAAAAAAAGGCTA | 10451 |
rs541761377 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107803267 | GTCAATATTGTTTAT[C/G]TTTTCAGAAAACCAA | 10451 |
rs541773317 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107960827 | CCTTGGAGAGGACTT[C/T]CTTGACTACCTTCTA | 10451 |
rs541775407 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107674188 | GCATTCAAGTTTAAT[A/G]TTTAGACTGGCAGAA | 10451 |
rs541778766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812901 | GGCCAAGGCAGGCGG[A/G]TCACGAGATCAGGAG | 10451 |
rs541785770 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107733422 | GTAGGCTTCAGAAGG[C/T]TGGTAATAACAAACT | 10451 |
rs541786921 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107716683 | TCATCAGGGATATTG[A/G]TCTAAAATTCTTTTT | 10451 |
rs541790241 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710209 | TAAGATGAGAACCAA[C/T]TTATGACATCATGCT | 10451 |
rs541796382 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107928716 | CAGAGGAGGCAAAAG[-/A]AAAAAAAGAATAAAC | 10451 |
rs541799384 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107766005 | GGAAACTGACTCTGC[A/G]AATCTAATACTCCAA | 10451 |
rs541802523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842716 | GCAGGGGGTGTCATT[C/T]TTACGCATTTTAATT | 10451 |
rs541809102 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107606459 | TATCTTCAATTTGGA[A/G]CCACATGTCCTTCGG | 10451 |
rs541815581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819632 | AAGTGAAAATATATC[A/C]CTTTTTAAACCTTTA | 10451 |
rs541830330 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868764 | TAATAAAGATTAACA[C/T]ATCTACAAACCTGAA | 10451 |
rs541831327 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107712951 | CAAGAGGAAGAATTT[C/T]GGGACAGAGGAAAAA | 10451 |
rs541831500 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107925378 | TTGAATTTGTATACC[C/T]GTATTCAGAGCAGCA | 10451 |
rs541834824 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107961555 | CACTGGCCAACTGCA[A/T]TTTATTTAACTGTAT | 10451 |
rs541846426 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107681917 | CGCCGGCCTTGACCT[C/T]CCAAAGTGCTGGGAT | 10451 |
rs541849067 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107656440 | AGATAGAGTATATTC[A/G]TGGTTACCAGAGGCT | 10451 |
rs541850591 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107916411 | GGTTTCAAATATATT[G/T]CAAGTAATATTTTAT | 10451 |
rs541857872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613844 | AGAATAATCAATGTG[A/G]AATAATTTTTTTAAT | 10451 |
rs541862132 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107934750 | ATGCTGTATTTAGCA[C/T]TTTCAAATATCACAT | 10451 |
rs541870467 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107679344 | CTTATCAATTTAATC[A/G]TTACCTATTCATTTA | 10451 |
rs541884883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107710734 | TTAAAATAATATGGA[C/T]AGTTTATCGCCAGGA | 10451 |
rs541884958 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107704187 | TTTAAGAACTAAAGA[A/T]AGAAGAATATATTCT | 10451 |
rs541891504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597138 | ATATAAAATTTCTTA[C/T]AAATATCTGAAATGA | 10451 |
rs541894922 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107911028 | CAAGGTAGGCTTGAG[A/T]CATAATCTCTCTCTA | 10451 |
rs541911444 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896255 | AATTGATAAAGCTCT[C/G]CACTTAGAGACACAG | 10451 |
rs541922869 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107717002 | ATTTATCCATTTCTT[C/T]TAGATTTTCTAGTTT | 10451 |
rs541933310 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107673562 | AGTATACCCTCTGTA[C/T]CTCCCTGATCTCAAA | 10451 |
rs541947535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107941096 | TTGCAAAGTGTCTTC[C/T]CCCTCAAAGCCTGGC | 10451 |
rs541974139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759404 | AAAATATTCTCACTT[G/T]GTGAATCTGTGGTTT | 10451 |
rs541981207 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107612895 | TTAGCTACCCTGCAT[A/G]GTACAATCCAGTGCC | 10451 |
rs541981814 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107612157 | ATACACACACACACA[C/T]ACATACAGAAATATT | 10451 |
rs541985096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933442 | TCCATCTACATTAAT[C/T]AGCTCACTTCAAGGT | 10451 |
rs541990856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107575709 | CTCAAGGCCACATTT[C/T]TTCTCATCTATGAAA | 10451 |
rs541996281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107709552 | TTTATTGTGAGAAAA[C/T]ATTTAAACTTTGATA | 10451 |
rs541996316 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939456 | TCTCGAAATGCTGGA[C/G]AGCGGCAGCAAGCAA | 10451 |
rs542008787 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948189 | CCAAAGTCTGAGACT[C/G]TGTACCCTCACCTTT | 10451 |
rs542013070 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571556 | GCTCCCTCCATAACA[A/C]AGTTCGGCTGACGGC | 10451 |
rs542019998 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107607172 | TGTTCCAGGCTGGTC[G/T]TGAACTCCTGACCTC | 10451 |
rs542020361 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107957055 | GGTATTAAGAGAGTG[A/G]GATGCATGAAACTGA | 10451 |
rs542025174 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107946488 | TGTTTCTCTGCACAC[C/T]ATCTGGCAATATGTT | 10451 |
rs542027754 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107574722 | CTGGTTAAGTGGCAC[G/T]TTCTTCCCTAACAAG | 10451 |
rs542032532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744020 | ATTTGTGGAGCTTAA[C/T]GGCTACATTCTCACT | 10451 |
rs542034251 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107661941 | TTACAGATTAGTTGA[A/C/G]GAAGGTATTTTCCTC | 10451 |
rs542050664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841094 | GGGAGACCACTCAGG[A/G]GAATGATGATGGGAG | 10451 |
rs542068966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677548 | TATCTGACGTTCTAA[A/G]TAAGGAACAGTTTAT | 10451 |
rs542088724 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107813365 | ACTTACTCCTCCATA[C/T]TGCCTCTTAGCAACA | 10451 |
rs542091674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107792946 | ACAGGACTGTAATGA[C/T]ATTCTGGTTTAAAAG | 10451 |
rs542095269 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107807118 | ACAGAAGGACGACTG[C/T]ACATTAAAGCCACAG | 10451 |
rs542102225 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107699094 | CTACCCAACAGTCCC[A/C]CAAAGTCTTAACTAA | 10451 |
rs542111852 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107903065 | GAAATGTATCTCCAG[C/G]CTTCTCAACAAAGTC | 10451 |
rs542114106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107846590 | ACCAAACAAATGGAA[A/G]CCAAAAATAAAGGAG | 10451 |
rs542115479 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590736 | ACTTGTACTAATTTG[A/G]TTTCAAATCCTTTAT | 10451 |
rs542115697 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107583364 | AAGACAAGGATGCCC[C/T]CTCTCACCACTCCTA | 10451 |
rs542122942 | snp | C/T | 0.000148572 | 0.00861767 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573319 | GTGCAGGGTGCAACA[C/T]GGGATTTGAATTTAT | 10451 |
rs542123043 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107582429 | TATTTTTTATTATTA[C/T]ACTTTAAGTTTTAGG | 10451 |
rs542124831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805466 | TGATAAATTTTGCAG[C/T]TCAGCAAATGTATTT | 10451 |
rs542127426 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107820182 | TCACAGTACTGTTCA[C/T]AGTATCTATGATTTG | 10451 |
rs542150264 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107903626 | CTCACTACAGAAGCT[A/G]AGTATGCATCTTTAT | 10451 |
rs542175320 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824447 | AAATGGATAATGACA[C/T]GTACATTTTCAGAAC | 10451 |
rs542175479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107816122 | GTTCCTAACAGGCCA[C/T]GGACCTGGTACTTGT | 10451 |
rs542181380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107684460 | ACACATTAGCCATGG[A/G]TTTCTCTCAGGGTTC | 10451 |
rs542182012 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888168 | ACACTGTTATTAACC[A/C]CACACTGTGATATCT | 10451 |
rs542195104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107691723 | GATGGTGACTCATGG[C/G]CCCTCAAGGGGTTTA | 10451 |
rs542206135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921057 | TCACCTTCACTCTGC[C/T]CCTTGCAAGATTATT | 10451 |
rs542207281 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107698124 | GTCAATAATACCAAC[G/T]TCACAGAATTTATAT | 10451 |
rs542208177 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107934383 | TAGAACAGAGCAGAA[G/T]ATATATTTTGCCACT | 10451 |
rs542210366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594759 | GAATTGGCTGGGAGT[A/G]AACCACAGAGTGAAA | 10451 |
rs542217287 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107869697 | CAGGTGGTATTTGGT[A/T]ACATGAGTAAGTTAT | 10451 |
rs542224547 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959930 | CATCCAGTTTCTCAG[A/G]GCAAAAATTCTGGAG | 10451 |
rs542225506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107781089 | GGAACTGGTACCATA[C/T]ATATATATGGTTGTA | 10451 |
rs542239020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649157 | GTGGACGTGTGAGTT[A/G]GCAGCCACAGGGAGT | 10451 |
rs542249486 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688590 | TTGGTTCTCTTACCC[C/T]ATTGGCTTGTCAGGA | 10451 |
rs542259884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695110 | CAGACATAAAAAAAC[C/T]GGTTGGAGAACTGTG | 10451 |
rs542274491 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107909449 | ATGAGTAGACAATGG[A/G]AAAAAAAATGGTCAC | 10451 |
rs542308199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738114 | GCAAGGACAGAACAC[C/T]AAACACCGCATGTTC | 10451 |
rs542311178 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783743 | ATTTAAAATGAAAAT[G/T]TATTGGCTTTTAAAA | 10451 |
rs542317446 | in-del | -/TAAAG | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107804693 | TCATAATTGCAGTAT[-/TAAAG]TATTCTGGGGCTGTA | 10451 |
rs542335967 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657096 | AGTAGCTGGGATTAC[C/G]GGCATGCACCACTAC | 10451 |
rs542338457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107600730 | ACCAATCCAGGTCAC[C/T]GTGGTATTACTGGCT | 10451 |
rs542342259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107882113 | ACTGAGGCAATGGAA[A/G]AGGAAAAATCTCTAC | 10451 |
rs542348294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656618 | AATTCAAATGTTCCA[A/C]GCATAAAGAAAAGAT | 10451 |
rs542349358 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107703530 | TGCTCATGCCTAGCA[C/T]AGAGAATGGCACAGA | 10451 |
rs542354267 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107821863 | AGAGCAAGGTCTCGT[-/A]TAAAGAAAGTGATTT | 10451 |
rs542357943 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107736287 | GAAGCATTCCCTTTG[A/C]AAACTGGCACAAGAC | 10451 |
rs542357974 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107595966 | TAAATATTAGCATAT[A/C]TTTTACGTTTCTGCT | 10451 |
rs542368503 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107841595 | ATTAACATACAAAAA[A/C]ACAAAGTAAAAGCAT | 10451 |
rs542369856 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107888617 | GTGCCCGCCAACACG[A/C]CTGGCTAATTTTTGT | 10451 |
rs542388744 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107633887 | CAATCCTGTGGACAC[A/G]GGCATTCGAGACCTT | 10451 |
rs542390555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831508 | TCTGGAATGATCTTT[C/T]CTCTCCTCACAATTC | 10451 |
rs542392146 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107722475 | TGACTTGAAACAGAC[A/T]CATGTGCCAGTGAGT | 10451 |
rs542393755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700732 | TGATTCCGTGCTTTT[A/G]CCATTGTGAATAGTG | 10451 |
rs542400334 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107847158 | GAAACCAAACAACCT[G/T]CTCCTGAACGACTAC | 10451 |
rs542404430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793748 | TTTTTAGCTGGAGAA[A/T]GAACTGTCAAACAGG | 10451 |
rs542405254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881665 | AAAATGGTAGAAAAG[C/T]ACTCAATATCAATGC | 10451 |
rs542407313 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107662774 | GGGTAGAAAAAGACA[C/T]ATTAGTCATATGAAT | 10451 |
rs542415006 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107609064 | TACCACTCACTAGTT[C/G]CATGCTCTGTTTCTT | 10451 |
rs542415975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751494 | AAGGGTCCAAATTAC[A/G]AGACGGTTCGGCAAT | 10451 |
rs542417062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886014 | AACTGAACATCCAAG[A/G]ATGAACAAAAAGGTC | 10451 |
rs542422901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923063 | CATTTCCATCACCCT[C/T]AACAGCTTGCAGAGT | 10451 |
rs542427255 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107838420 | TCACATCTGGTCAGG[G/T]TGGCTTTTATTAAAA | 10451 |
rs542448986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107796352 | CCAACTCCTATCAGT[A/G]AGCAAACAGCGAACC | 10451 |
rs542455803 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619015 | TGATCCCATGGTAAG[C/G]AAAGGAATTGGAGGG | 10451 |
rs542456035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936056 | GGGGAGAAAAGTAAA[C/T]GTAGGACATTATTAC | 10451 |
rs542463924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107715789 | ATTCTAGAGAATTTG[A/G]ATTTTCTCATTCTCT | 10451 |
rs542468852 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893981 | CACCATCAACACATC[A/G]GTTCTGTAAAGAAAG | 10451 |
rs542508627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107604644 | AGAGGGGTCTTCTCT[A/G]ACCATACCATCTAAA | 10451 |
rs542524743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802780 | TCTGTGTTTATCAGT[A/G]ATATTGGCCTGTAGT | 10451 |
rs542528269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767278 | TAATTTTCAGTCAGG[C/T]AGTAAATACATGTCA | 10451 |
rs542537427 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107776611 | CCATAGCATTTGAAT[C/T]TGTCTTGGGGCATAA | 10451 |
rs542542450 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107666894 | TTGAGCAAGGTCACA[A/G]AGCTGGTAAATAGTG | 10451 |
rs542547537 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676394 | ACCAGCTGTGGGGAC[A/C]ATGTACATGAAGAGC | 10451 |
rs542557506 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107578047 | GTTAATACTCTTGTC[A/G]TGAAAGGGTCCTAGT | 10451 |
rs542568803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107856924 | TGTGCCTATAGTCCT[A/G]GTTACTTGGCAGGCT | 10451 |
rs542570876 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107718601 | TGCTCATGGATAGGA[A/C]GAATCAATATCATGA | 10451 |
rs542572010 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107598719 | TTGCGCAGACAAGGT[A/G]TAGAATTAAATTCTA | 10451 |
rs542573800 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107681261 | AAAAAATCAAAGGAA[C/T]TTCCATGGTAGAAAT | 10451 |
rs542574109 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107770785 | ATATATTAACCTATC[A/G]GGAAGTAGAGATCAA | 10451 |
rs542578295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107865771 | CTGTCAGGTGAAGGT[C/T]TGGCAATTATCACAC | 10451 |
rs542594500 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107577355 | CGCAGGCAGCTATAT[A/T]AATTGACCTGCTGAT | 10451 |
rs542605637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673615 | AGGACATAGGGAGTT[A/G]TGTGAGGGAAAACAC | 10451 |
rs542615139 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107769021 | GTCTCTCAGTTCCTT[G/T]ACCACAAATAATCTT | 10451 |
rs542615502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858890 | CTTGAAACTATACAG[C/T]TGTTTTAGGCAGGGA | 10451 |
rs542620395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107873186 | AGCATACAGTTTATG[C/T]TTTCACATTCAATTT | 10451 |
rs542622250 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761450 | CTCTAGTGCAAAATC[A/G]TGGCCCCCCAGGGTC | 10451 |
rs542624856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769700 | TCACAAATTTCACTT[G/T]TTCCAACAGACTCCT | 10451 |
rs542637266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107680500 | GCATTTACTATATAC[C/T]GGGCACCTTTGAGAG | 10451 |
rs542637882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107906621 | CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA | 10451 |
rs542640449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107857736 | GGGAAGTTATCGACT[A/G]ACTGTGCCTGATTCC | 10451 |
rs542659890 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107851735 | AGAAGATTTTTTAAG[A/T]TGCATCTAATGTCAC | 10451 |
rs542662025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802203 | TTGCATGTTGGTTTT[A/G]TATGCTGCAACTTTA | 10451 |
rs542669234 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107699976 | TCACACACCAAAGGT[C/T]ATGAGGCTGAGGAAT | 10451 |
rs542674647 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694368 | TTGGATCGACTGGAT[C/T]AGGCAGTAGATTTTT | 10451 |
rs542701560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107645397 | CACTTCCAATTTCAG[C/T]ATGATCTGTTGTCAG | 10451 |
rs542703977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107808901 | CTGATAATAAATTCC[C/T]AGAAGTGAATAATTT | 10451 |
rs542707533 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107625661 | AGCGGTCTATTTTCC[A/G]AAGCACATAAAGGTT | 10451 |
rs542708389 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107651136 | AGAAGACAGCCATCT[A/G]TAATGGCCCTTGCCA | 10451 |
rs542710215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107637273 | CTACCAAACTCACTC[A/G]AGGAGAAGAAGCAAG | 10451 |
rs542719937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107735821 | ACTATTCCAATCAAT[A/G]GAAAAAGAGGGAATC | 10451 |
rs542724350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586057 | AAAATGAGACTATAG[C/T]TTTGTTTTTCATCAC | 10451 |
rs542726072 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107609551 | AAAACTATAAAAAAT[A/T]AAAAAAAAAACTACT | 10451 |
rs542739268 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879552 | CACAACATTACTTGA[C/G]TGTTTTTTTTTCCCA | 10451 |
rs542746320 | snp | A/C/G | 0.00231314 | 0.033931 | utr-variant-5-prime, intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964906 | GCTGGGCCGGGGCGG[A/C/G]CGGCAAGGATGCGGC | 10451 |
rs542751628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107653413 | CTTTTATTTATAAAA[C/T]GGTGCTACAATTAAA | 10451 |
rs542755990 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107740170 | TGCGTGCCTATAATC[A/C]CAGCTACTCAGGAGG | 10451 |
rs542758646 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107740242 | CACTGAGCTGAGATC[A/G]CGCCACTGTACTCTA | 10451 |
rs542761344 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592898 | ATCTAAGGCAGGTTT[C/G]AGATGACCATTTTGG | 10451 |
rs542765303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107881866 | GTTAGCAATATTGAC[A/G]CTTAAAAAAGGAAAC | 10451 |
rs542780277 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872606 | CAGTTCCATTACCCA[A/C]AAGCTAGGACCTATA | 10451 |
rs542781960 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107746091 | GCAGCAAAATTTGAA[-/C]CATAGGCAAAATCAA | 10451 |
rs542786693 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107871313 | TTTCAAAACATAAAC[C/T]CTCAACGTCCCCCAT | 10451 |
rs542790914 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107774736 | TTAGGAAACAATGAT[G/T]GCCTCCACAGTGGGG | 10451 |
rs542797531 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107783382 | TGAGGCACTGGAACC[A/C]AGATGGCTGCAGTAG | 10451 |
rs542800735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107878776 | CATGTCCCCCCTTTA[G/T]AGCAGTAAGTAACCC | 10451 |
rs542811119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686129 | ATCTTTCTTTCCCTC[A/T]AAAAAAAAAGGGATT | 10451 |
rs542814489 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107735213 | ATTTAAAGCAGTGTG[A/T]AGAGGGAAATTTATA | 10451 |
rs542814917 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659695 | GCTTCTACTATACAT[A/C]AGCTATTATGTATAG | 10451 |
rs542820110 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107703705 | ATTCAATGTCCACCT[C/T]TTCCTTTGGGAAAAT | 10451 |
rs542823814 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107849931 | ATGAACAGACACTTC[C/T]CAAAAGAAGACATTT | 10451 |
rs542829534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773804 | TACCACATCAAAGGA[C/T]AGGAAGGTCTGGTGA | 10451 |
rs542829602 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782629 | CTGGCACTCAGTTTT[G/T]TGTCTATGCTATTGT | 10451 |
rs542841880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107652103 | TAAGTCACAGGATAC[A/G]CTAGGAGGTCAGCAC | 10451 |
rs542842409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107789786 | TTTAATTCAAGATAC[C/G]TAGAATATTATCATT | 10451 |
rs542855351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700218 | TTGTTTCATGGTCTA[C/T]GCAGTCAACTTTCAA | 10451 |
rs542865412 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964157 | GTTCTTCCCTTTGAC[C/G]AATGTCACTCCTGGA | 10451 |
rs542867114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107935490 | CAGTGGTTGGAGAAA[A/G]TGAAAAGCCAGGTCT | 10451 |
rs542889324 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107615414 | TATGCAGGACTGAAG[A/G]TGAACCCCTTCCTTA | 10451 |
rs542900485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107843835 | CGTACCCCTACAGAG[C/T]GGGGAGCTTTCCACT | 10451 |
rs542905125 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107651006 | ATGAATGAAAGAGGT[A/G]GAGCCTTTGAGAGGC | 10451 |
rs542906340 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917867 | TTTCCTTTGAGCCAC[A/T]TATTGGTACTCAAGA | 10451 |
rs542910383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107788915 | GTTCAATACCAAGAA[C/T]GGGAATGTATTTACA | 10451 |
rs542913502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107877055 | CTTTACCCTTCACGG[G/T]AATCATTCTCAGAGG | 10451 |
rs542916713 | in-del | -/A/AA | 0.20205 | 0.245358 | intron-variant | VAV3 | GRCh38.p7 | 1:107951812 | ATTATCAAAAAGTCA[-/A/AA]AAAAAAAAAACATGC | 10451 |
rs542921099 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694291 | TCCTTGGAACTGTTC[A/C/G]GAGAAAAGGGAGCAT | 10451 |
rs542928383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885249 | GACACATAAGTCTGT[C/T]GCTTTTATTTTTTAT | 10451 |
rs542935988 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107834701 | ACATACTTTGAACAG[A/G]TCTTTGGAGAGAAAG | 10451 |
rs542949263 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107884165 | AAAAAGTTAAAAAGA[A/G]TAAGACCTAGTATTT | 10451 |
rs542982671 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107696902 | ATCCTAGGCCAGTCA[C/T]GAAAAACTATATTAC | 10451 |
rs542985912 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107630555 | AACACTCAGCAAAAT[-/A]AGCTATTATTTCCTA | 10451 |
rs542988008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107870840 | ACTCTTTAAGAAAAC[A/G]TATCACTTTACACTG | 10451 |
rs542989145 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964468 | GGACGCAAAGCTTTC[C/G]CATTCAGCTTGAGGA | 10451 |
rs543032249 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107942640 | TCTTTTCAGTCTACT[A/G]CTGCTTCTTTTCTGA | 10451 |
rs543037906 | snp | G/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107668901 | TTACAGAGGCATGCT[G/T]TAACAGTTAGTTCAC | 10451 |
rs543054287 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107608935 | ATTCAGTCTTTTTAA[C/G]AGAAGTCAAACACAA | 10451 |
rs543056949 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107883559 | AATGTAGCAATGTGT[C/G]TTTTTAAACTTACCT | 10451 |
rs543059682 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107700714 | ACTGATGGGCATTTG[A/G]GCTGATTCCGTGCTT | 10451 |
rs543063948 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107850299 | CAGCACTATTCACAA[A/T]AGCAAAGACTTCAAA | 10451 |
rs543088536 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107789558 | CGCTGGTTTGGTAAC[A/T]GTGGTCATTTCATAC | 10451 |
rs543091354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107608382 | AGAGAAGAAACCTAA[A/T]CATCACACTTTCAAG | 10451 |
rs543109924 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107760212 | CTTTGGAGCAGAACT[A/C]ATGAGTCTCCTGGTA | 10451 |
rs543111602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107830503 | TTATCACAAACAACC[C/T]GCTGGCACAACTACC | 10451 |
rs543128329 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814776 | GATGAAAACAGTGCT[G/T]ATGGAAGAATATTCT | 10451 |
rs543135015 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107724008 | AAAGTCAAGCAACTT[A/G]TCCAAGGCTCGTGAA | 10451 |
rs543145259 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729762 | GAAAATATGAATTAT[A/C]TCATTGGACTGATAC | 10451 |
rs543148935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107768327 | AAATAAATAAATAAG[A/G]CCAATATTCTTAAAT | 10451 |
rs543179399 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107761931 | TCACCCTCTTCTTTC[C/T]TAAAGGTTTATTTTA | 10451 |
rs543191470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942553 | TTCCTTTTTATATCT[A/G]TGTATCCTGACTTAA | 10451 |
rs543193548 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107934858 | CTAAACAAAATATAG[C/T]GGCACAGCGAGGCAA | 10451 |
rs543198837 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107918726 | TTTTTTTTTTGAGAG[A/G]TGGAGTTTTGCTCTT | 10451 |
rs543204528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891737 | CCAGCTACTTGGGAG[A/G]TTGAGGCAGGAGAAT | 10451 |
rs543208057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107729282 | GTACTATCAGAGAAC[A/G]GATCCCTGAGTTCAT | 10451 |
rs543209345 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107825457 | TAGTACCCTCGCGGG[-/A]AAAAAAAAAAACTGC | 10451 |
rs543213643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864347 | AGGGCAAGGGCCAGT[C/T]GTGGTGGCTCATGCC | 10451 |
rs543233990 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911326 | AGCTATGTATAAAAC[A/T]TAAGCTTAATACAAG | 10451 |
rs543256404 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107844089 | ACCAATGCAGAAGGC[A/G]GGTGATTTCTGCATT | 10451 |
rs543266905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711101 | GAAGGATAAATATTG[C/T]AAAAAAGTACACAGA | 10451 |
rs543270626 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699270 | TCCAAATGGGAGAAA[C/T]TGATCAAAACAAAGG | 10451 |
rs543271283 | snp | A/G | 0.021333 | 0.101051 | intron-variant | VAV3 | GRCh38.p7 | 1:107718215 | TGGCCAGGGCAATCA[A/G]GCAAGAGAAAGAAAT | 10451 |
rs543275825 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107599504 | CAAGGAAACAGGCAA[C/T]GGAGATGGTTTATAA | 10451 |
rs543278804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107577277 | AAGTGATGTGACTCC[A/G]GGGTACCTGCTCTTA | 10451 |
rs543293432 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107854141 | TGGCAAATCCCCATC[A/T]CTGCTAAAAAATACA | 10451 |
rs543296326 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107672131 | AAACTTAGCTAGGCA[C/T]GGTGGCACACACCTG | 10451 |
rs543329690 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107717748 | TTCTGTAGATGTCTA[C/T]TAGGTCGGCTTAGTG | 10451 |
rs543331641 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673082 | AAAGTATGTTCATGC[A/T]CAGATGTTCCTCAAA | 10451 |
rs543339339 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821164 | TTGTTATCATATCCT[G/T]AGAAGACAAAATCCT | 10451 |
rs543339806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107629992 | AGCATAACTTCTCAA[A/G]AATTTCCAAATAAGC | 10451 |
rs543342184 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107852847 | ATGGTTTATCAGCAA[C/G]CACTCTATCTAAAAG | 10451 |
rs543354395 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107941989 | CCCTAGACTGTCTCC[G/T]CCTAGAATACCCCTC | 10451 |
rs543360144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107801562 | CAATAGCTGAGTGTT[A/G]GCCAATCTCAGAGGC | 10451 |
rs543366528 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686534 | TGGTATAGGGTGAGA[C/G]CTGCTTCTTAATATT | 10451 |
rs543381770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962964 | CATTGTATGTGCTCA[A/G]TTTTCATTAATGATG | 10451 |
rs543388886 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107666809 | CTCGTTTAAGCCTCA[C/T]GACAACCCTATGAAG | 10451 |
rs543412017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107771182 | TAAGATTGGAAGTCA[C/T]AGAGCACAACACTAA | 10451 |
rs543417421 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948434 | AACCAAGTGACCTTG[A/G]TCAAACCATTGTATA | 10451 |
rs543438633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783643 | CACCCACTCCTCCAC[A/G]GAGCCTTCTCTGGCC | 10451 |
rs543439586 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107768085 | ACATCACCTACAAGA[C/G]AAGGTCTGAGGGTCT | 10451 |
rs543441032 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107694290 | GTCCTTGGAACTGTT[C/T]GGAGAAAAGGGAGCA | 10451 |
rs543442468 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107920174 | ACTGAGAAGGGAATG[C/T]AGCATAATGCTCTGC | 10451 |
rs543470932 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107943708 | GATGGTGCCACTGTG[C/T]TCCAGCCTGGCAACA | 10451 |
rs543473727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783259 | TCACAGGGTCAAAAC[C/T]GCCTTTTTAAAGCAA | 10451 |
rs543476829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910870 | CTGCAATCCCAGCTA[C/T]TCAGGAGGCTGAGAT | 10451 |
rs543477663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700329 | AAGTTCCAGGGTACA[C/T]GTGCAGGATGTGCAG | 10451 |
rs543482250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591979 | TTGTATCACATCTTT[C/T]ATAGCAACATATATA | 10451 |
rs543495527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814180 | ACCCAGTCAGTAGCG[A/G]AAACTGCTGGATCAC | 10451 |
rs543498100 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107797127 | TGTCAGGAATTCTAC[G/T]TGAACCTGTGAGGTA | 10451 |
rs543510647 | snp | C/G | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965577 | GCGCTGAAAGTTTTA[C/G]AGATCGTCGCCCCCT | 10451 |
rs543530093 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107846415 | AATTTACACATAACA[A/G]TATTAACCTTAAATG | 10451 |
rs543532135 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107885185 | CCAGAAGGAGGGGAG[A/C]TGGGGTTTTTCCTCA | 10451 |
rs543537675 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107685194 | TGTGTTCTTACACCT[A/T]GAATTTAGAATTAAA | 10451 |
rs543547468 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107821236 | GTTATAGCATGTGTA[G/T]TCACTGATTTGGCAA | 10451 |
rs543554821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731710 | GCAGTCCGTCCCTCA[C/T]CACAAGAGGCATCCA | 10451 |
rs543566167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107650940 | GGCACATATACACCA[C/T]GGAATACTATGCAGC | 10451 |
rs543567785 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107780663 | TGGGATTACAGGCAC[A/T]CACCACCATGCCTGG | 10451 |
rs543573557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107746966 | CTCACTGCAACCTCC[A/G]CCTCTCAGGTTCAAA | 10451 |
rs543593255 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107884459 | ATTATTATTTTGAGA[C/G]AGGTTCTTTCTTGCT | 10451 |
rs543605886 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107782047 | TGCTTTACTTTAGCA[C/T]GCATCTTATCCTAAT | 10451 |
rs543607159 | snp | A/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589861 | TCTATTCTATTGTAA[A/T]ATAACTAATAAATAG | 10451 |
rs543607920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107692784 | TAAACAGATAAGCAA[A/G]TGGGGATCTGCTTCA | 10451 |
rs543609836 | in-del | -/CTTAA | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572071 | GGGCCAAGTTAGTGT[-/CTTAA]CTTGACTGCCTTGAA | 10451 |
rs543611192 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107820346 | ACATTATGCTAAGTG[A/T]AATGAGCCAGGCACA | 10451 |
rs543613296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107754618 | GCTTCCCACTGCAGT[C/T]ACAATAAAATCCCAA | 10451 |
rs543632952 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107736441 | TTGCAGATGACACGA[C/T]TGTATATTTAGAAAA | 10451 |
rs543636426 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903110 | GAAAAGAAAAAAATC[A/G]AAGTTAAGACATGGG | 10451 |
rs543637608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107926110 | CATGGTGAAGCCCCA[C/T]CTCTACTAAAAAAAT | 10451 |
rs543644691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795482 | TCTGTTTTGGTACTA[C/T]TGTCTGTTTTCTTTT | 10451 |
rs543649560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107754110 | TATCCACAATGTAAA[A/G]TTTACGGGCAGTTAT | 10451 |
rs543663856 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107709105 | CAGCCTCCATAACAC[-/T]TTATGTAACATCTGA | 10451 |
rs543678816 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107922809 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 10451 |
rs543681363 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802126 | GCTATTGCAAATGAG[A/C]TTGCTTTCTTGATTT | 10451 |
rs543698099 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107882647 | CTTCTCTATATCTCT[C/G]TTTTAAAATTAGGTG | 10451 |
rs543705300 | in-del | -/AAACC | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107806259 | TTTTTCCAGTGTTAG[-/AAACC]ATGAGTTGTGGAACA | 10451 |
rs543707084 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107873901 | GGCTTCCCCATATGC[A/G]CTGTATTTCAGCATC | 10451 |
rs543710729 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664395 | TTCCTCGCCACTGCC[A/C]TGTGTCCACATGTTC | 10451 |
rs543713700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107891263 | GTGTCAAGCCTTGCA[C/T]GGCAACTCCAGGTAG | 10451 |
rs543716298 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107665550 | ACCAGGTGTTTGTCC[G/T]CAAAGGAGCTATCAG | 10451 |
rs543734923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107582186 | CAGTCTAGGAGGTTC[A/G]TTTTGCCAAGATTGT | 10451 |
rs543735929 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107605477 | TCACCAGATGCAGCC[C/T]CTCGATTTTGGACTG | 10451 |
rs543759418 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107827633 | ATCCTTTCCAATAAT[A/G]TTCCAGAAAGCTATT | 10451 |
rs543760154 | in-del | -/G | 0.000450214 | 0.0149968 | intron-variant | VAV3 | GRCh38.p7 | 1:107765181 | ATAACCAATCTGAAA[-/G]GGGAAAAAAGACAAG | 10451 |
rs543764644 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636974 | CCAAAAGAATAGAAA[G/T]AAAGTAATAAAAATC | 10451 |
rs543786525 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107757876 | TCCCCTGATTTTACA[A/T]ACTCTACAAATTCTA | 10451 |
rs543789259 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761015 | TCTGTAAATAACAGA[A/G]AGTATCTTCAATTTA | 10451 |
rs543797455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107581307 | CTTAGGTAGGTATCT[A/G]GTTATTTTGCATGTG | 10451 |
rs543802772 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107949425 | AAGAGATCCTTCCAC[A/G]TCAGCCTCCCAAGTT | 10451 |
rs543817862 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV3 | GRCh38.p7 | 1:107682709 | ATACCACTTATGATA[A/G]GAAAACAAAATGAAA | 10451 |
rs543821261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107760464 | CTGCAATATTGAGGT[A/G]CTCATAAATAAATAC | 10451 |
rs543822429 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953298 | TTGGGGAGGCAGTGG[G/T]GAGAAGGAAGGAAAT | 10451 |
rs543828636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107723515 | ATTCTCCATCTGGGC[A/C]TGGCTGCTTGACACA | 10451 |
rs543841546 | snp | G/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107756714 | GTCTGTCTTTTCTAT[G/T]CATAATTTTCGTATT | 10451 |
rs543849897 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107863971 | GTACAGTCAAGTTTT[C/T]TCTCTAAAAGTTTAA | 10451 |
rs543856732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107773754 | AATCTGGCCAGAGAA[C/T]ATTAGGGCAGGTAAA | 10451 |
rs543872603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732226 | TGCTGACTTGAAAAT[A/G]TAAGTCTTGGGCAGC | 10451 |
rs543875705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107636306 | AGTGGAGATGGGCCA[C/T]AAAATAATTCTAAAT | 10451 |
rs543888151 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635535 | AAATGAGAAGTTAAT[G/T]GGTGCAGCACACAAA | 10451 |
rs543889747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107643487 | TCTAGGTGCAGCAAT[A/T]CTGGTCACAATGGAC | 10451 |
rs543891396 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107801149 | TAGGCTTATATCTGG[A/G]TGGTCTATTCTGTTC | 10451 |
rs543891533 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729112 | AACTACTTATGACCT[C/G]AGGTATATTTTGTTA | 10451 |
rs543898213 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107776532 | GGTGTAAAGGTCACA[A/G]GGCTAAAACAAGCCC | 10451 |
rs543900833 | in-del | -/CTT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107888432 | ATGCCTTTCAGCAGG[-/CTT]CTTCTCTACCCTGAG | 10451 |
rs543903747 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107908378 | TCTCATTTCTTGATA[G/T]CCTCAAAGTAAGATC | 10451 |
rs543915379 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591293 | TTGTGATTATTGAAG[G/T]TGTTTGTTTTTGTCT | 10451 |
rs543916592 | snp | C/T | | | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896035 | CAGGAAGTAACTCTC[C/T]GTGCCAGAGGTGCTG | 10451 |
rs543951173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107598535 | TATTTCTTCCTTTCT[C/T]CCTTGGGCCCAGATA | 10451 |
rs543952833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107734664 | AGAAGAGCTAACTAT[A/C]CTAAATATATATGCA | 10451 |
rs543973626 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107713457 | AATACACAAGTACCA[C/T]TGAAAGTCCATAAGA | 10451 |
rs543998082 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107778087 | TCTACTCTTTTCAGG[A/C]AGCCAGCATATCACA | 10451 |
rs544000700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107734067 | TATTCAACATTTTTA[A/G]AGAACAGAATTTTCA | 10451 |
rs544002278 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689529 | TTTTTTTCTTTTTTT[C/T]CTTTTTTTAACGAAT | 10451 |
rs544005237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698570 | CATCATTAATGGAGG[A/C]GCAGCTGTACTGAGA | 10451 |
rs544020568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777491 | TCTGGGGTTCCCCTA[A/G]GGAGGCTGTAACACC | 10451 |
rs544023114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917605 | CAAGAAAGACATTGA[A/G]TCTCAAACATGCTAT | 10451 |
rs544040894 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV3 | GRCh38.p7 | 1:107873891 | CAGGTAGAGTGGCTT[C/T]CCCATATGCGCTGTA | 10451 |
rs544049789 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107815036 | GGAATGGAAAATTCC[A/G]TATCAGTTTTCTTAT | 10451 |
rs544057643 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107784571 | TGAAAAATATCTGCA[A/T]AAATTTAGACACCCC | 10451 |
rs544063318 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107852436 | TAGCCACTGAAAAAC[A/G]AACACAGTTAACATT | 10451 |
rs544064073 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898764 | AAATATGTAAGTAAA[A/C]TATTCATGCAACAGA | 10451 |
rs544068398 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107704092 | ATTCAATTCATTAAT[G/T]CATGAATTAGTCTGT | 10451 |
rs544068647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107606334 | TTCTAATTCTTTGTA[C/T]GTTGCCTGATTTTTT | 10451 |
rs544073284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595658 | CCATAACATGCTTTT[A/G]TTTGCATGCTAATCT | 10451 |
rs544077536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695828 | AAAGGTCAAGTAAGG[C/T]AAGGCCTAAATGTGA | 10451 |
rs544101435 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914748 | TCATTTTAGTGCTTA[C/G]TTAGTAGGCATGGTC | 10451 |
rs544103274 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613540 | ATTTTCATATATACC[A/C]AATTAGTGTCTTCCT | 10451 |
rs544106190 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107871030 | ACAGACAGCTCAGTA[C/G]GAAACATTTCCAAAG | 10451 |
rs544122972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738883 | AATCTCTACACTACT[C/G]AGACAAGCCGGAGAC | 10451 |
rs544125671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107880880 | TTGGTGTTGTAGTGA[C/T]GTTTCGGTGCTTGCT | 10451 |
rs544126661 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107745411 | GGGGGGGAATCCTCC[G/T]GCCGTATCCAAGTGG | 10451 |
rs544133651 | in-del | -/TTTATTTTT | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107609405 | CTACTAGTGTCAACC[-/TTTATTTTT]AGAAGCAGTGGCTCA | 10451 |
rs544164306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107668174 | TCTCACTTCCTCCCT[C/T]CATTGAGCATCTGGC | 10451 |
rs544169905 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107759086 | CTGTACCTTACATGT[A/G]CCTATCATATTGTGT | 10451 |
rs544186997 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107677840 | TCTGATTCTGAAGGT[A/G]CCTGACCAGTATAAA | 10451 |
rs544201941 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | VAV3 | GRCh38.p7 | 1:107581556 | AGTTATCAGCATAGC[A/C]ATAATAACTGACTGG | 10451 |
rs544208161 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107853012 | TTTTTTTTTTAATTT[G/T]TATTGATTTTTGCCA | 10451 |
rs544215490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107741906 | AGAATTGCCCATCCT[A/G]CTTGGTTCCAAAAAT | 10451 |
rs544215965 | in-del | -/AAGAATCTTCTCCAGTTATTAT | 0.00755907 | 0.0610114 | intron-variant | VAV3 | GRCh38.p7 | 1:107731584 | AAACTCATTATAAGG[-/AAGAATCTTCTCCAGTTATTAT]AAGAATCTTCTATAG | 10451 |
rs544216231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771590 | GAATGAATCACTAAA[C/T]TTCTCTGACTCAGTT | 10451 |
rs544224108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588989 | GGAAAGGCAATACAA[C/T]TCATTGAAAACACTT | 10451 |
rs544227889 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107709925 | TTAGCAGTGTGAGAA[C/T]AGACGAATACAATAT | 10451 |
rs544229595 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720745 | AGGTTATGAAGATAC[A/G]TATCCTCTACGAGCC | 10451 |
rs544240884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812030 | GGGAAAAAATGACAG[C/T]CTCTATAACAGCAAG | 10451 |
rs544242478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107853910 | ACAGCCACTCTTTCA[G/T]ATCTGAACCCCCTGT | 10451 |
rs544252692 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107839474 | TTGAAATATTTTAAC[C/T]ACATGAAAATCAAGC | 10451 |
rs544254326 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107726834 | ACTGATGGTTTACAG[A/C]GTGGGTACACAAAGT | 10451 |
rs544264203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107633528 | TTAGGGCTGCTCATG[C/T]GGCTTCAAAATGTTT | 10451 |
rs544271251 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107845183 | TCTGGAGTAGACCTC[A/C]AGCCAGACCTGCAGC | 10451 |
rs544276276 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107640510 | TGGAGGGATTACCAA[C/G]GGGCACAAAAACTTT | 10451 |
rs544281864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818534 | AAAAACAAACTATAA[C/T]ATGATGGTATTATTT | 10451 |
rs544301952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107652241 | ACTGCTACACTCCCA[C/T]CAGTGCCATGACAGT | 10451 |
rs544302278 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107893842 | TTCTTCTTCACCATA[C/T]CTAACTTTTTTCCTG | 10451 |
rs544312193 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107797262 | CACTTCAGCTTTCTT[A/C]TAACACTAGTTTGCC | 10451 |
rs544316940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726517 | TTATCTACATAATAA[C/T]GCTCTGGCTTCTTGT | 10451 |
rs544327097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107617051 | TTCATTTATTCTCCT[C/T]TTATCTGTGTTTTAT | 10451 |
rs544327532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732358 | TCATCTCACTGGGAC[C/T]GGTTGGACAGTGGGT | 10451 |
rs544347013 | in-del | -/A | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107887071 | GATGAAACACTTGTT[-/A]GTATGTTTTTACTAG | 10451 |
rs544348287 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702229 | TGAGACAGAGAGCAA[C/G]AGCAAGAAATACTGC | 10451 |
rs544350115 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571273 | GCAAGACAAAGTATA[C/T]GGAAAACATTTACTT | 10451 |
rs544351603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875224 | CCAAGGCAATTTCTA[C/T]CCTCATGAAACTTAC | 10451 |
rs544353798 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819233 | GAAATTCTTTCTTCC[C/G]TTGCTATCATGCAGA | 10451 |
rs544354023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737099 | GACAAAAAGAAGAAA[C/T]GGTGGAAGGATTCCC | 10451 |
rs544354992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900619 | ATTTACAGAGGGATC[A/C]CTGCCTGTAAACCAC | 10451 |
rs544356231 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107817015 | ACCAAGCACCCACAA[C/G]AGTGTTCCTCCAATA | 10451 |
rs544360292 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107866992 | GTGATACCTAAATAG[C/T]ATGATATCTAAATAC | 10451 |
rs544371457 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107960119 | TAGCCTGGCCACTTC[A/T]ATCCTTGCTGCTCTC | 10451 |
rs544375345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603216 | ACCTGGAAGAGAACA[A/G]AGGCTAAAAGTAAGT | 10451 |
rs544380946 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107858696 | AAACCATTCCCCCAG[A/T]ACTCGGTCCATGGAA | 10451 |
rs544383064 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107825287 | GCAAGTATCATCACA[C/T]TTATGGGTCTTTATT | 10451 |
rs544387091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107731827 | GAATGTATGAATTTA[C/T]AAAACTGTATAGTTT | 10451 |
rs544395766 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719278 | AACAGGTAACCTACA[A/G]AATGGGAGAAAATGT | 10451 |
rs544413143 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107631000 | GACAGCCTTGAAACA[C/T]TGTAAGATCTTAAGT | 10451 |
rs544418542 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107674288 | CAGTGCCAGTGTCTA[C/G]AGTTGTTTGTTTCAG | 10451 |
rs544419970 | snp | A/G | | | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690147 | TTCAATTCAAAAATA[A/G]TTATTTTTTTCTGAT | 10451 |
rs544431240 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107681756 | CCTCCCGGGCTCACG[C/G]CATTCTCCTGCCTCA | 10451 |
rs544440904 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107638886 | TACATATACATATAT[A/T]TGAAGATATATATAC | 10451 |
rs544441858 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107823909 | ACAGCTCTCCAAGAA[A/T]CCAATTTGCAAACAC | 10451 |
rs544444331 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107659521 | AAGTATGCAGAAGCA[C/T]TGACAAAGTGATTGT | 10451 |
rs544452793 | snp | G/T | 1.87696e-05 | 0.00306341 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107602460 | TCTTGTTAAAATCTT[G/T]ATGTGCTTTGCTTCA | 10451 |
rs544455985 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107610512 | AACATGCAAAATAAA[C/T]AATATACACTGGATA | 10451 |
rs544464225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107791933 | TGACTTCTAGGAGGA[C/T]GGCAGGTAAATGACA | 10451 |
rs544473168 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107930172 | CATTTAATAACTAAA[A/G]GAGTATAACTGGATT | 10451 |
rs544495939 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107902275 | TAAAGTGATTAAAAG[A/G]CCATCTGTGATTGAA | 10451 |
rs544501537 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107753817 | TGCCCGCCTCGGCCT[A/C]CCAAAGTGCTGGGAT | 10451 |
rs544503437 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786926 | GTTATAGATCCCTTT[A/G]AGAGTATGATGAAAG | 10451 |
rs544510575 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107725400 | TGATAACAAGTGGAA[A/G]TATGCAGCCGAAAGT | 10451 |
rs544513775 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107824796 | AAGTGGTTAGTCACA[A/G]TGATTTACTAGGCCC | 10451 |
rs544515806 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107736814 | AATGCCATCCCCATC[A/C]AGCTACCAATGACTT | 10451 |
rs544516084 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832971 | TTTAAAAAGTTTGAT[A/G]TAACAGTGAAAATCT | 10451 |
rs544529806 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107873300 | ATTTTAAAGTATTTA[C/T]ATATTTTTCCAACAT | 10451 |
rs544550863 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832541 | ATCATTTTCATTTCT[A/T]TCTGAGTCTTTTATA | 10451 |
rs544555199 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107817574 | GCTAAGCTTTGAAAT[G/T]ACTCAAATGGAAGGG | 10451 |
rs544559501 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107810552 | ATTTATAAAACATCA[C/T]AGTCCCATCTGAATT | 10451 |
rs544568342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107741131 | TCCGACAGCTTCATG[A/C]AGATACTGTAGGCAT | 10451 |
rs544575105 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107838931 | AGATGGGAACAATAG[A/G]CACTGAGGACTACTA | 10451 |
rs544578714 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572253 | GCTGGAGGCCCACAA[A/C]AGTCCACTGACCCTC | 10451 |
rs544589324 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107784659 | TGACAACGGAAAATT[C/T]CTTAAGGGCAGTAGA | 10451 |
rs544592178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588209 | TTACTAATGAAGATG[C/T]GCAATTGCAGTTGAT | 10451 |
rs544593763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936876 | CGCTGCTCCTTCCCC[A/G]ACCGATCTTGTGATT | 10451 |
rs544594508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107645312 | TGAGTTTATGATATA[A/C]TGGAATGTATTTTTT | 10451 |
rs544594743 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593993 | TTTAGTCCTCAGAAC[C/T]ATCTTAGTCTTCCTC | 10451 |
rs544595435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707639 | GACTTATATGCTCAG[G/T]GTCCTTGGGACTAGG | 10451 |
rs544621217 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107865516 | AATATTAATCTGGTG[A/G]GTCATGATGATTTAT | 10451 |
rs544632817 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595568 | CAATTTTTTTGTTAC[A/C]TGCTCTATCTCCAGG | 10451 |
rs544632871 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587669 | CATCTTGGCTCACTA[C/T]AACCTCCACTTCCTG | 10451 |
rs544648201 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842045 | TAATAAATTTTTCTA[C/T]ACTACCATTGCTCAT | 10451 |
rs544648203 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107719828 | TGTCCAACAATGATA[C/G]ACTGGATTAAGAAAA | 10451 |
rs544658791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107714244 | AAGCTAGCTGGACCA[C/T]GCATCTAACTTACCA | 10451 |
rs544662580 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107796436 | CAAGACATGTATACT[A/G]GGGCCAATGTACTTG | 10451 |
rs544671440 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107713707 | GATATATAACCAATG[G/T]CTTCAACGACATCCT | 10451 |
rs544687857 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621256 | GGCATTCTGTAGATG[A/G]CAGAGAGGTGAGAGA | 10451 |
rs544692409 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107816782 | AAAAGAAATCTATAA[C/T]AATGTTTATTCAAAC | 10451 |
rs544700940 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107770329 | GCCTTATTTTTCTTC[A/C]GAAAACTTATGACCA | 10451 |
rs544716599 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914587 | TACAAACGGGAAGTA[A/T]CTCTGTTCTTATAAA | 10451 |
rs544735838 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107646396 | GTTACAGTGTTGCTC[A/G]CCCAAATATGAATAT | 10451 |
rs544739805 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777388 | CCCTCACTAAATATG[C/T]AAGTTGTCTGCTGCC | 10451 |
rs544752400 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107951035 | CACCAAAGATAGGTA[C/G]TTCAATGTCTTTCCT | 10451 |
rs544752818 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107713810 | ACTCAGTAAAACCAA[-/T]TCTATGAGGGGCCTT | 10451 |
rs544757215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936160 | AATTGATAGATAAAA[C/T]ATCCTGAAAATACAC | 10451 |
rs544757837 | in-del | -/CT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107808785 | CATTTAGTCAATACC[-/CT]GTTATTGAACAAATG | 10451 |
rs544773873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731760 | AAGAAGTTGTACGAA[A/G]GACTCAAGCAGTGAA | 10451 |
rs544782443 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107601452 | CCTTACACTCAGTTT[A/G]ACTTTAATGTTAACA | 10451 |
rs544792771 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107943728 | GCCTGGCAACAGAGC[A/G]AGACTCCGTCTCAAA | 10451 |
rs544802563 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107784466 | TCTTTTCAATTATGT[C/G]CAGATTTTGCTATAG | 10451 |
rs544803331 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | VAV3 | GRCh38.p7 | 1:107681345 | TACTGATCCCTTGTT[C/T]AAACATTTTGTCTGA | 10451 |
rs544807798 | in-del | -/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107663943 | ATTGTTCTTATGATA[-/T]GAAAAAAATTAACAA | 10451 |
rs544835512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921310 | TCCAGTCTTTAAACT[A/G]CATCACATACTTTAG | 10451 |
rs544841092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832400 | ACAGGAAGAACCTTC[G/T]AAAATGTTTGGAATT | 10451 |
rs544848330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769181 | CTCCATCATATCCTC[A/G]TTTCCCTCCTAACCG | 10451 |
rs544850180 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107653852 | CTATGAATATACATT[A/G]ACTGAAAAAATTGCT | 10451 |
rs544850670 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586937 | CAGAAAATAGGGTGT[G/T]TTGTGTGGTATTGAA | 10451 |
rs544856613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939749 | GATTTAGTTGGTGAA[A/G]TGATCCTGAGGAGCA | 10451 |
rs544865128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107809659 | ATATTCAAACAACAT[C/T]CCAAAACAATAGCAT | 10451 |
rs544879932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107873237 | ACAAAGCTTCCGTTG[C/T]CTAATCAATCTAGCA | 10451 |
rs544880607 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107724825 | GGTTGCAACACTGGA[C/T]GTGGTGGGGGGAAAA | 10451 |
rs544883054 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107814195 | AAAACTGCTGGATCA[C/T]ACAATAGTTCTATTT | 10451 |
rs544884528 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107949501 | ATAATTGTAGAGATA[A/G]GCTCTATGTTGCCAA | 10451 |
rs544893990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886093 | CTGGCCAAAATTTTG[C/G]AGGAAATGCAGGAAT | 10451 |
rs544895980 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107597506 | TCTTGGAAGGGAAAG[G/T]TCAAAGGCAGGAGAG | 10451 |
rs544913858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815476 | ATGATGTGATTTTAC[A/G]CACTGTTCCAGGCTG | 10451 |
rs544917571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107609684 | CATTCCTTTCTGTGG[C/T]TGGTATAAACTTTAA | 10451 |
rs544930963 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595385 | AAAGTTATATTAAAC[C/T]GACGCAAATTCTGTT | 10451 |
rs544932886 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107886721 | CCACCCATGCTGGAA[A/G]CTTCCATCAAACTGC | 10451 |
rs544933981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107936824 | ATTTATGCACTTATG[C/T]CTCATCGCAAACCAC | 10451 |
rs544944352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107706939 | GAACATCCACAGGCA[C/T]ACACATGAACATACC | 10451 |
rs544946736 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107952135 | CTGTGGAATACTATG[A/C]AGAATGAGATCATGT | 10451 |
rs544948330 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908697 | TCCATGTTAAAAGGA[A/G]AGGACTACTGAAGAA | 10451 |
rs544955610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107892516 | CTTTTCTGATTTTTC[C/T]AATTCTCCTTCCCCT | 10451 |
rs544958385 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107660425 | TAGAAAAGAAACTAA[C/T]TCATGTGGCAGCTCC | 10451 |
rs544959668 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107666973 | TTGATTTTCAAAAAG[C/G]CATCATAAGCCAAAC | 10451 |
rs544977008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107796399 | TTTTCCTTTTTTTAG[A/G]GATCAGTTCTCTTAG | 10451 |
rs544985663 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107648651 | AACACAATTACACAA[C/T]TTTACAGAGTATTGT | 10451 |
rs544993053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819137 | CAAAATAGATTGCCT[C/T]CAGGAAACCAAGTAT | 10451 |
rs544998779 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107859960 | GTGATAAAGATATTA[C/T]GGTTATATAGAAAAA | 10451 |
rs545001974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107852228 | ATGAAATTCCCTTTT[C/T]AGTTTCCCTGTTCCT | 10451 |
rs545036013 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107900797 | TGTGGTCTCTGAACT[C/T]AACAGACATATCTTA | 10451 |
rs545041236 | snp | A/G | 0.0002027 | 0.0100652 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755380 | AACTCCTAGAATGTC[A/G]TTGATGTGGGGGTGA | 10451 |
rs545041368 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107789333 | TGAAATGCAGAAAGT[C/T]TCAGAAAGAAAAGGC | 10451 |
rs545043518 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107738622 | GATTGCCAGTTTCCA[A/G]TCGCAGCTTATTTTG | 10451 |
rs545049527 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107570920 | ATCTGCACCTGCGGC[A/G]GCTCTGCCCGGGCCC | 10451 |
rs545061525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107850884 | TATATATTTCCTTTC[A/G]TATGGCTGCATAGTG | 10451 |
rs545081664 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107674259 | CTGCTGGGTGTCATA[C/T]ACATGGCGTGTTTCA | 10451 |
rs545095491 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786729 | AAAGGATAGTACACA[A/G]GATGGGCTCAGAGAA | 10451 |
rs545100847 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907346 | ATTCTAAAGAGCCAT[G/T]CAAAAAGATGTTGAC | 10451 |
rs545105175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107602316 | GTGAGCAAAATTTCC[A/G]AGAAACTATAGAATT | 10451 |
rs545108390 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965663 | CTCCTAGTTGCCCCT[A/C]GTGGTGTTTTGGCAC | 10451 |
rs545121552 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688773 | CAACATGCCTCGTTT[C/T]AAGAATCTAAAAACA | 10451 |
rs545124546 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107639035 | AGATATATATACACA[C/T]ATATGTATGGACAAC | 10451 |
rs545124637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107646998 | ATTCTAAGTAGAACC[C/T]TATTAGAAAATTTTC | 10451 |
rs545138358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107761513 | ACCAATTTCCCCCAG[C/T]GGACTTATAGAACAG | 10451 |
rs545142715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736755 | GGATAGGAAGAATCA[A/G]TATCGTAAAAATGGC | 10451 |
rs545145638 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107578115 | CCAGACACCACCCAA[A/G]CAGACTGGCCAAGAG | 10451 |
rs545154167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107823637 | GAGACTGTCTGTTAA[C/T]GGACCAAATGTTTGT | 10451 |
rs545155765 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107906523 | CACAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC | 10451 |
rs545174952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769117 | ACTTCATATGCTTCA[C/T]AGCACTAATTTCAAG | 10451 |
rs545179563 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | VAV3 | GRCh38.p7 | 1:107736338 | CTCCTATTCAACATA[C/G]TGTTGAAAGTTCTGG | 10451 |
rs545188979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831757 | GGCTCCCAGCATCAT[C/G]CTAGTATATAATAGA | 10451 |
rs545192570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107637962 | AAAAACAAAAATTAT[A/G]TCATCATTTCAATGG | 10451 |
rs545196935 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107725815 | ACCGTGCCCAGATGG[A/C]AAATTTCAGTAGCTA | 10451 |
rs545200187 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107795790 | AAAGAATATATGAAT[A/C]CTTTTGATTTGGCCA | 10451 |
rs545202907 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107681336 | ACTCAACTTTACTGA[A/T]CCCTTGTTTAAACAT | 10451 |
rs545204852 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761498 | ATCGCTGTACTTCCC[A/G/T]CCAATTTCCCCCAGT | 10451 |
rs545226506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107839407 | TCTAGATATCTGTTA[A/G]TTAAAGAACACACTC | 10451 |
rs545233904 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107887522 | AATGTAAATTCCACT[A/T]TTTTGTCCTTCTATC | 10451 |
rs545245160 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107696349 | AATATACAATAAATT[A/T]TTGTTAATTATAGTC | 10451 |
rs545246284 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107928677 | TTAGTGAGCTTGACA[A/G]CAGGCTAGCTGAAAA | 10451 |
rs545263015 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107881601 | ATGCGTAGCCTCTCT[C/T]CCTCTTCAGAAGGGC | 10451 |
rs545265029 | in-del | -/GCA | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107862202 | CCAGAGGAAGCCTGC[-/GCA]GCAGCCGGACTCCAC | 10451 |
rs545265965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107687739 | AGTATTTAATGATGG[A/G]CAACTTGCTGTTTAC | 10451 |
rs545286478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107775827 | TCAAGGCCACCTACC[C/T]TGGAAAGAGCTGCTG | 10451 |
rs545292548 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107671840 | TTGTTTAAAACGTAA[C/T]TTCCTATATATACAG | 10451 |
rs545297477 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107910817 | AAACCCCATCTCTAC[C/T]AAAAATACTAAAATT | 10451 |
rs545301686 | in-del | -/GTT | 0.00993419 | 0.0697739 | intron-variant | VAV3 | GRCh38.p7 | 1:107874742 | TTTTTGTTGTTGTTT[-/GTT]TTTGGTTTTTGGTTT | 10451 |
rs545304446 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107616985 | AGTATCATAACACAC[C/T]AGGGAGTACATTTTA | 10451 |
rs545307086 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107730418 | CTAAAAGCAGAACTT[A/T]AACTCTGAGACTAAA | 10451 |
rs545307839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107652157 | GCTGATAAAACAGAT[C/T]GCAGTAAAGAAGCCG | 10451 |
rs545315280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107740949 | CTTGTTCTAAGAGAC[A/G]AAATTTGTTGTCTCA | 10451 |
rs545318024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107879590 | CATTCTTTGAGATTA[A/G]AAGTTATCTGCTAGA | 10451 |
rs545319809 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107833162 | TAGACAAGTAGTGAA[G/T]GTAAAGGAAAAGTTA | 10451 |
rs545327903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783221 | AGCTAGGAAGGACCA[C/T]TGAGAAAGTGTGGAA | 10451 |
rs545334418 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107659776 | TTGTTGAAGGCTTCT[C/T]TTTATACATGAGTTA | 10451 |
rs545350581 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911407 | ATGATAGTAGGTCAC[A/C]CATGTAGTGATGCCT | 10451 |
rs545351483 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107720099 | TAGCATTAGGAGAAA[C/T]ACCTAATGTAAATGA | 10451 |
rs545359560 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107671694 | AGGAGCTACTCTGAA[C/T]TCAAAAGGCAGAGCC | 10451 |
rs545360124 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107838606 | ATCCAATTACTGGGT[A/G]TACAACCAAAGGAAA | 10451 |
rs545360370 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963669 | GTAGCTGAGGCTCTG[C/T]GTCATAGAGGATTAG | 10451 |
rs545364052 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107727231 | CCATGGCCAAGTCAG[C/T]GATAGGGTTTGGGTT | 10451 |
rs545369019 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107822400 | TGGCTCATGCCTGTA[A/T]TCTCAGCACTTTGGG | 10451 |
rs545373391 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107878404 | GCATTTGGCAGTTTT[A/T]TCTTTTAGTCAGTAT | 10451 |
rs545375826 | in-del | -/T | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689521 | TAGCTTTTTTTTTTC[-/T]TTTTTTTTCTTTTTT | 10451 |
rs545388337 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107616338 | GAACTAACACAGGAA[C/T]GGAAAAGCAAGTAAC | 10451 |
rs545403538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759350 | CTTTTACTTCATTAA[A/C]TAAAAGTCATGTTAT | 10451 |
rs545408474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107844132 | ACCCAGCTCATTTCA[C/T]TGGGGCTGCTTAGAC | 10451 |
rs545414564 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV3 | GRCh38.p7 | 1:107577590 | CAGCTTCTGGGACCT[C/T]TCCTAACAATACAGT | 10451 |
rs545426973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107718839 | AACCAAAACAGCATG[A/G]TACTGGTACCAAAAC | 10451 |
rs545444340 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107643049 | GATGCCTGCTTCATA[A/G]AAAACACATCACGTA | 10451 |
rs545447335 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620611 | ATGTCACTTTTTTTT[G/T]GTTCACACAGACAAG | 10451 |
rs545457868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107575384 | TTACCCTGGAAGAGC[C/T]TGCCCACTTGGCCAC | 10451 |
rs545459480 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802861 | TTTGTGGAATAAGTT[G/T]GAAAGTATTTCTTCC | 10451 |
rs545459703 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107889519 | TGTGGTGAACCAGGA[C/T]AATGGTCTTCCTACA | 10451 |
rs545467579 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107899168 | TTCCTAGATGACTTT[C/T]TTCACAATGCAGTTA | 10451 |
rs545480547 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107718667 | AATGCCATCCCCATC[A/C]AGCTACCAATGACTT | 10451 |
rs545483656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107628061 | ATAGAAGCCTTTTTG[A/G]TTCTGAGAAGACGTC | 10451 |
rs545485145 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107577558 | GCCAATGGAATATAA[A/T]CAAAAGTGTCATGAG | 10451 |
rs545489321 | snp | G/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787184 | CAGGGTTAGTACCAG[G/T]TCCCTTTTCTTCTGT | 10451 |
rs545494955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107809602 | TACATTAAGGGAAAG[A/G]ACCAGAAAATATATT | 10451 |
rs545498048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933375 | GATATCTTAGACTCA[C/T]TGCTCTTGAAAATCT | 10451 |
rs545506736 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107619655 | TCTATTTTGCGAGGA[A/G]AGGCCAAAGAGAGAG | 10451 |
rs545511328 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589365 | AGAGAAAAGAAGGGA[C/T]AATGATACACACAGA | 10451 |
rs545517083 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV3 | GRCh38.p7 | 1:107634753 | ATATCCAGAATCTAC[A/G]ATGAACTCAAACAAA | 10451 |
rs545524493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793926 | AACAGGGATCCACTT[A/G]ACTTGCGTACTGCTG | 10451 |
rs545524610 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107846246 | TACAAACAAGCAAAT[A/G]CTGAGAGATTTTATC | 10451 |
rs545532977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107847517 | ATTAACAAAATAGAC[C/T]GCTAGCCACACTAAT | 10451 |
rs545539598 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107714133 | GACCAAAGGAGACCT[A/G]AAGCTGTCTGAACTA | 10451 |
rs545540268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107957148 | TCTCACTAAAATGTG[C/T]CCCTTCTTTATGACA | 10451 |
rs545540651 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107748570 | ATATATGCATTTACA[-/T]TATCTGTTTGTGTAT | 10451 |
rs545541968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107724720 | CAGCAGAGAACAGAT[C/G]CCGAGCCAGTAAAGA | 10451 |
rs545548344 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950892 | GAGGTTAGAGAGAGG[A/C]GAGAGAGCAAGCCTC | 10451 |
rs545551823 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107784339 | ACTTTATTCATTTTA[C/G]TGCTGTGTAACATTT | 10451 |
rs545573203 | in-del | -/AAT | 0.0142736 | 0.0832652 | intron-variant | VAV3 | GRCh38.p7 | 1:107609547 | TCTAAAACTATAAAA[-/AAT]AATAAAAAAAAAAAC | 10451 |
rs545574632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107815392 | GAGTTCCAGAGTGGA[A/G]GCTGAAGTACAGGAT | 10451 |
rs545593735 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107857848 | TCCTTTTAGATCAGC[A/T]GGAGTTCGAGAGAGA | 10451 |
rs545599451 | in-del | -/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107699737 | GATTCTTTCTCTCTC[-/T]TTTTTTTTTTTAAGT | 10451 |
rs545601898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107686725 | AAAAAACTGATGTTA[C/T]ATATTTTTAAAAATC | 10451 |
rs545602047 | in-del | -/TTAT | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107650545 | TAAATTTTTATTTTA[-/TTAT]TTATTTATTTATTTA | 10451 |
rs545606298 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107626300 | ATCACCCAGGGAAAA[C/T]GTTTCTTACAGGCCT | 10451 |
rs545618164 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107637320 | ATGTTTGTTTTATAA[A/T]TTTTTTTTTTTAAAC | 10451 |
rs545634774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676857 | CATTCATAACCTATA[C/T]GACACACTTTGGTAG | 10451 |
rs545638942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107954034 | TCAAAAGGAACTACT[C/T]TGCTGTTCATGGTTC | 10451 |
rs545650438 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107724135 | ATTAGGAAAATGGTA[C/T]CTCCAATCATAGTAT | 10451 |
rs545664069 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107829716 | GCATATATGAGAACT[-/A]AAAAATGTGAAACTT | 10451 |
rs545666275 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107618159 | AGTAACGCTTGCTCA[A/T]TGGCAGCTCACCTCC | 10451 |
rs545674105 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107641484 | CATGAAATTCGAGAA[C/T]TTAATGAACAGCTTT | 10451 |
rs545679625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107729820 | CAAAAATTATTTTTT[A/G]TTGTTTACCATAACA | 10451 |
rs545685300 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107919399 | CATGTGGCTGATAAG[C/T]TCTGATGGTTTACGT | 10451 |
rs545686806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107733355 | GGATCGCAGCTCCTC[A/G]CCAGCAATGGAACAA | 10451 |
rs545692319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107854752 | AATCACGAATATGAT[A/G]GGAGGGTCTCTTCTC | 10451 |
rs545700020 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107735261 | GAGAAAGCAGGAAAG[A/T]TCTAAAATCGACACC | 10451 |
rs545716666 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107634194 | AAAGAACAAAGCTGG[A/G]GGCATCATGCTACCT | 10451 |
rs545723733 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912624 | CCCTTCTCTGATCTC[A/T]CACTTCACAAATATT | 10451 |
rs545726461 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107964324 | CCCTCCCCTTCGTTA[C/T]TATAGAAGAGCTTGA | 10451 |
rs545741234 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771762 | CAGCTGAGTGAGGAC[G/T]GCCCTTGCGGGAGAC | 10451 |
rs545748016 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737683 | CCAGTTAGAATGGCG[A/G]TCATTAAAAAGTCAG | 10451 |
rs545768374 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107961679 | CATGAAAAAATATAC[C/T]TATTTTTGAACTGAA | 10451 |
rs545771590 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107848121 | GATCAAGACCATCCT[A/G]GCTAACACGGTGAAA | 10451 |
rs545783831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107619930 | TTCATTCTGTTCCTC[C/T]TCCAAAACTCAGTTC | 10451 |
rs545784454 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107778101 | GCAGCCAGCATATCA[C/T]ATGTTTCATAAAAAC | 10451 |
rs545786758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107632069 | CTGACTTCCACAATG[A/G]TTGAACTAGTTTACA | 10451 |
rs545797380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107940148 | TGGGTAGAATTGTAG[A/T]GGTTTTTGTTGTTTT | 10451 |
rs545801737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710137 | TTATAGAATAAAGGA[A/G]GCAAATCCTAGCAAG | 10451 |
rs545806782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818843 | CCCTCCCCTCTCGAC[A/G]TGCTACCATCATTTA | 10451 |
rs545809406 | in-del | -/ACAA | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107573435 | ACTTCAAAGGATTCT[-/ACAA]ACAGAGTATTTTGTT | 10451 |
rs545826788 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107800571 | AGGAGGTATATGTGC[A/G]GATTTGTTACATGGG | 10451 |
rs545835117 | snp | C/T | 1.64827e-05 | 0.00287073 | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107596273 | CTCCTTGTATGGAAA[C/T]TGCAGAGTTGTATCT | 10451 |
rs545836252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107612119 | TGAGAATATAGTATC[C/T]GTACAAAATTATATA | 10451 |
rs545840087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842264 | CCACTACCTTGGACA[C/T]AGCTGAATGGCAAGG | 10451 |
rs545843371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107826085 | AGGTCTCCACTTGTA[C/T]AAGTTTATCTTGTTA | 10451 |
rs545847263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107574585 | TTGATGGCCCAGTAA[C/T]CTAACCAGCACCTCC | 10451 |
rs545870145 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107659271 | ATTTTTGAAAATACC[A/G]TCTTTCAGAAAAAAA | 10451 |
rs545898197 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107908779 | AAGCAGTTGTTTTTT[A/T]AAATTTACATCACCA | 10451 |
rs545906131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721761 | GATGATGCTTTAACA[C/T]CAAACTACACAAACT | 10451 |
rs545906548 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896817 | CTGTTTTTGTTATGT[A/G]TTAGAGGGGAAATAT | 10451 |
rs545915153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107603443 | CAGTGGGTATTGGGT[A/G]AAAAGACAGTTGTGG | 10451 |
rs545919723 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107873574 | TTAGAGAAGTGTCCA[C/T]CTCACCTGTGATTCA | 10451 |
rs545926581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107947250 | AGACAAATCGACAGA[C/T]TCAAATGTGCCAATT | 10451 |
rs545930206 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107833264 | CACAGTGAAAGTTTT[C/T]GTGGTCTGGATAGAT | 10451 |
rs545930284 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107641652 | TATGAATAATGCCCA[A/G]AGCACCTCTGAGAAC | 10451 |
rs545937159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107684221 | ATGCATGGCTACATA[C/T]TTTATTTCTAAAGCA | 10451 |
rs545958018 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107842855 | AGAAACAGTCTCTCC[A/G]ATGAGAGAAATATTA | 10451 |
rs545960779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107939645 | TTTCTCAGGACATAA[A/C]CCCATCTAAGTCATG | 10451 |
rs545969761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945599 | GAGGTTGAGACGAGC[A/G]GACTATCTGAGGTCA | 10451 |
rs545972797 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107812811 | AAGCAGGAAGAGATA[C/T]AAGAATACAGGAATT | 10451 |
rs545984654 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107662124 | TATTTAAAGAGGCTG[G/T]GTTATTTTTAAAAAA | 10451 |
rs545996713 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107818591 | TACATACCCCCAGGG[A/T]TTCATCTCCAAAAGA | 10451 |
rs545999624 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107954745 | CTCCAAGGGAGCCCC[A/C]CACAACAGGAAAATA | 10451 |
rs546003865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107772417 | ATTTACTTTTATAAG[A/C]GTATAATTTCATGAT | 10451 |
rs546009625 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107582501 | TGTGCCACGCTGGTG[C/T]GCTGCACCCACTAAC | 10451 |
rs546013293 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107743060 | TCTCTAAGAACTGAA[A/G]CACACAATCTAACTA | 10451 |
rs546019982 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107950045 | CAGCCTGGGTGCTGC[C/T]GGGAACTGAAAAACG | 10451 |
rs546024099 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946560 | TTTCGCATTGGAAAA[A/C]AAAGCTGAAGGAAAA | 10451 |
rs546032931 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107715100 | TTGGCCCATAAACTA[A/T]TCTTTCTATTTTTAG | 10451 |
rs546037660 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107581869 | TAATCGACACTCTTC[A/C/G]TTCAGGTACTAGTTA | 10451 |
rs546045349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720681 | AAAACTCCATCTCAA[A/G]AGAAAAAGTGTAGTG | 10451 |
rs546046439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590032 | GCATGTTGTTGGATG[A/G]TGAATAGAATAATGG | 10451 |
rs546053994 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107931200 | TGTTAGATTATAATA[A/C]GAAATTGCTCACTTT | 10451 |
rs546056748 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107951843 | TGACAAGATTATGGA[A/G]AAAAAGAAACACTTA | 10451 |
rs546057931 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107679071 | TGTGCTTAATGTCAG[A/G]TAAGAAATGAAATTG | 10451 |
rs546061304 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107960323 | TACAAAAAAGTAGCC[A/G]GGAGTAGTGGCACGT | 10451 |
rs546067073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107708256 | TAGTAAGACAAGCGT[A/G]GATATAGTAGGACCA | 10451 |
rs546087995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107648462 | TGTTCTGTTATACAT[A/G]TACATTTTATTGGAA | 10451 |
rs546103774 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107674891 | CTGATGAAGCAAGCA[A/T]CCATGGTGAGTAGGT | 10451 |
rs546106899 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107719987 | CACCGCATTTTCTCA[C/G]TCATCAGTAGGAATG | 10451 |
rs546119765 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107931412 | CACAATTATTATATG[C/T]CAATTAAAAATAAAA | 10451 |
rs546120460 | in-del | -/TTTG | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107709345 | CTTTTACTGTAGTAT[-/TTTG]TTTGTTTTCAAAAGC | 10451 |
rs546122159 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107798179 | AAGGGAAAATTCTAA[C/T]GAGGCTGAATTCATA | 10451 |
rs546154570 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572496 | CTGTAAACAATGCCA[C/G]CTTCTTCAGGTTATT | 10451 |
rs546160601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804781 | TTTTGTTTGTTTGTT[C/T]TGCACATTAATCTTT | 10451 |
rs546168579 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107826260 | CAAGCTGGAGGAAAA[C/G]AATCATTTGCTCCAT | 10451 |
rs546172563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702578 | TGAAATAATTACCTA[A/G]GAACAGACACTGAGA | 10451 |
rs546201973 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107632575 | CATAACGCAATTCTG[A/T]CCCAAGTTACATCTG | 10451 |
rs546207571 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107922723 | TTTGGGAGGCAGAGG[C/T]GGGCGGATCATGAGG | 10451 |
rs546212462 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107923840 | TAACCATATCAAGGC[C/G]CAAGGGGACTCATTT | 10451 |
rs546229434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107696706 | TGAGTTTGTCTTAAG[C/T]CAGTAGTACTCCCTT | 10451 |
rs546230823 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107802703 | CCACTTGATCATAGT[A/G]AATGGTCTTTTTAAT | 10451 |
rs546234068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881319 | GACTGTGTGTGGGGA[C/T]GCAGTGGGAGAGAAA | 10451 |
rs546253908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915565 | GGAAACAATACCTCT[C/T]CACAGAGTTATTTTG | 10451 |
rs546260430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107930671 | CCTAAAAAATTGTTT[C/T]AGGCAAAGATTAATA | 10451 |
rs546267364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881001 | GAGGCTTAGAGATTT[A/G]CCAACATTTACATAA | 10451 |
rs546270619 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107855732 | AATAGTATGAGGACT[A/T]CAAAACCTAATGAAA | 10451 |
rs546291198 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107842583 | AGCTTTTTAAACTGT[C/T]CTTGTTCACAGCAAA | 10451 |
rs546303130 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107662661 | CAGGTTATGTGCTGA[C/T]GTTTTAGCAAGAACA | 10451 |
rs546317002 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107860569 | TTGGTATGATGATAG[C/T]GTCCCTTTCTTTAAA | 10451 |
rs546322172 | in-del | -/ACACACAT | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786985 | CCCACCTATCTACAC[-/ACACACAT]ACACACATACACACA | 10451 |
rs546322873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107675921 | TGGAATAAACCTTTG[C/T]TGGGAATCTCCAGTT | 10451 |
rs546336115 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107707884 | GAAATGTCAGGATTA[A/C]AGATTTGGAGAAACA | 10451 |
rs546341539 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107799281 | AATCAGTTTCTTTAT[C/T]TGCCTTTTCTGTTTT | 10451 |
rs546353195 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107573182 | TTAGAAATCTCAGCA[C/T]TAAGACTTAGGAGGG | 10451 |
rs546353713 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107680174 | TATATGTTTTCAATA[C/T]TGGGAGTTTTTCTTT | 10451 |
rs546353736 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107714798 | CGTACAGTCTTTTAT[C/G]CAGGGAAATGAATAA | 10451 |
rs546354800 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966897 | ATCACCATTTAACAC[A/C]GTCTTTCATAAAGAG | 10451 |
rs546365702 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107764441 | ACCATATTTGTGTTC[A/G]TCTTCTCTTCCTTCC | 10451 |
rs546378509 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107895036 | CTGTTGCCCACCCAA[A/G]TGCTTAATGAGAGAA | 10451 |
rs546386537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107669274 | CTCTTCTTTATCCTT[C/T]GCTGTGTAAGTGGGG | 10451 |
rs546395391 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107887733 | GTACCACTACGATAC[C/T]CCAACCCATACACCA | 10451 |
rs546401946 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107846543 | ATGCAAAGACACACA[C/T]AGGCTCAAAATAAAG | 10451 |
rs546411788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107668490 | TAAAGCATGTAAAAC[C/T]TCTAGTACATCAACA | 10451 |
rs546428206 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804478 | AAGTCATTTTACAGA[A/G]ATGACAACTTATCAC | 10451 |
rs546446199 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107898166 | CATTTTGGAAAATAT[G/T]GGGGAACGAGTATCA | 10451 |
rs546456910 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107756922 | AAAAAATATGATATT[A/C]AATAATTCCCCATGG | 10451 |
rs546457196 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107675685 | AAGGATGGCACCTTT[C/T]TTCAATTCTGTCCCC | 10451 |
rs546457965 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107681870 | TTTCACCGTGTTAGC[C/T]AGGATGGTCTCCATC | 10451 |
rs546462775 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107680805 | AAACTATGGCACAGA[C/G]AGAGGAGGCAAACTG | 10451 |
rs546471438 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107579385 | AATGTGTCTGAAACC[-/A]AATTCCTCAACTTAT | 10451 |
rs546479037 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107864818 | GTTTATGCTTTACCA[A/G]TTTGTTTCCTTAACT | 10451 |
rs546491888 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107694419 | GTCATCAAGCATTCT[A/G]TGAATTGCTTCATTT | 10451 |
rs546493279 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107763859 | TTGAAAATCACCTGC[C/T]CCTTCTCCCCTGACC | 10451 |
rs546496592 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107647290 | GCCCAATTTAAAATC[A/T]AAACACAGCCACATT | 10451 |
rs546498605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900949 | ACCTTGTATATTTTA[C/T]GTAAATAAGATTTTT | 10451 |
rs546498901 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107668317 | TTCTTCTAGTTATGG[A/T]AACACATATATGGAA | 10451 |
rs546531041 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107620501 | AGGTGTGTAGTAGGC[G/T]ACACTATCTAGGTTT | 10451 |
rs546541145 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107611643 | AAGGAGACAGGAAGG[A/G]GGAGAGTAAAGAATT | 10451 |
rs546546784 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107907478 | TCCCCCAAAGTTCAC[A/G]TATTGAGAACTTAAT | 10451 |
rs546559336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107938902 | ACAGAGTTTCAGCCA[A/G]TCACAGAGTTTCAGC | 10451 |
rs546559863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107646468 | ACATGTACTTTCACC[A/G]TATGTATTTGGGCAA | 10451 |
rs546566673 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107764232 | ACTTTCCCAACTGTT[C/G]TGGTCAATACATACC | 10451 |
rs546567061 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107810828 | AATGGGTGAAAAACA[A/G]AAACAATACGCGACA | 10451 |
rs546578184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777558 | CACCACAGTCACATG[C/T]GCAGGGGGTCATAAT | 10451 |
rs546578545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107769965 | TCTTGCCTCAGAAGA[A/G]CCAGAATGAGAGGTT | 10451 |
rs546593117 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726403 | GATACTTTTCATGGA[C/G]AGGTGTGGACCGCCA | 10451 |
rs546594118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107669545 | TGGATCCATTCCTAT[A/C]TTTGATACTCGGTAG | 10451 |
rs546597090 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | VAV3 | GRCh38.p7 | 1:107918995 | TACAGGCACGAGCCA[-/C]CCCGCTGGACCAAGG | 10451 |
rs546601911 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587807 | ACGTTGGCCAGGCAG[G/T]TTTCAAACTCCTAAC | 10451 |
rs546614216 | in-del | -/TTTG | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107944602 | AACAAAACGCAGTTT[-/TTTG]TTTGTTTGTTTGTTT | 10451 |
rs546615252 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107777110 | ATCGCCAGTTTAAGG[A/T]TAATCAGTAATTAAG | 10451 |
rs546623974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107618598 | ATGTGCTAGACACTG[C/T]TCTGAGTGTTTTATT | 10451 |
rs546625633 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107750332 | ATTTCTTTTTTCTTA[C/T]TAAGAACAACGTAAC | 10451 |
rs546629615 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107809024 | TTCTAAACTATTCAC[A/C]AGGCTGAGCGCAACC | 10451 |
rs546633826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107840644 | ACGTGCCCTAAAGAA[A/T]CGTAAAGGAAGCAAC | 10451 |
rs546635287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107715264 | TGAGAACATATATGT[A/G]TGCATTTTAATAAAT | 10451 |
rs546640366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107841142 | ATAGTGAATGCCATA[C/T]GGTCTTAAATTCATT | 10451 |
rs546649082 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107731633 | TAGTAAAATCTTCTT[C/T]ATTATAAGGAAGAAT | 10451 |
rs546653222 | in-del | -/TG | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107725661 | CTGGGATCACAGACA[-/TG]TGCCACCACACCAGC | 10451 |
rs546658910 | snp | A/C | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107688847 | AAATTATACATAGTA[A/C]AACATTTCGTGTGAA | 10451 |
rs546663504 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107866701 | GATGGTGCACACTTG[C/T]AGCCCCAGCTACTCG | 10451 |
rs546673761 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107744884 | CCTCAACTGTACTGT[A/G]AATGATACAGCATCA | 10451 |
rs546690300 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804986 | TTTTTTGATTCCCCT[G/T]GCAGCACTTTGAAAA | 10451 |
rs546700507 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840844 | CAGAGACTCCTAAAA[C/G]CAAGTGTGAAGAACT | 10451 |
rs546710192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107914244 | GCCAGCAGAGCCAGA[C/G]AGAAATGTACCCATG | 10451 |
rs546711154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107872839 | CTCTTAACGTTGTTA[C/T]AATTTTACAAATTAT | 10451 |
rs546711455 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107625497 | GTTTCAAACTCCTGA[C/T]CTCAAATCATCCACT | 10451 |
rs546715467 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107741311 | GCTTAATTTTGAATT[G/T]CTGGGTAACATGACA | 10451 |
rs546720347 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695319 | ATTATGTAAGAATAA[A/G]ATTAAGAGCAGGGAA | 10451 |
rs546738441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107653761 | AACTATGTGTCTTCA[C/T]TTTTTGAAAATAGAT | 10451 |
rs546739863 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107720794 | ACAAGGCCCACATAC[A/C]TCAACAATTTGTGAA | 10451 |
rs546746178 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107625077 | CATTATCCTCACCTG[G/T]GAAACACAGAGCACG | 10451 |
rs546755453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107748798 | CCTAGGAGACCAAAG[A/T]TATCAAGCAGCCAGC | 10451 |
rs546757690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107740615 | AAAAATAAAAGAAAA[A/C]AAAAATCACACTTCT | 10451 |
rs546758326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107749870 | CAGAGTTGTTGAAAG[A/G]GCCAAGTGAGATAAG | 10451 |
rs546784721 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107939181 | ACACTAAGATAACAG[C/T]GCCAATTTTAAATAT | 10451 |
rs546786852 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107944744 | CGAGTAGCTGGGACT[A/G]TTGGCGTCCACTACC | 10451 |
rs546792705 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | VAV3 | GRCh38.p7 | 1:107852403 | AAAATAGAAAAGGAA[A/T]AAAAACCACCTCAAA | 10451 |
rs546794667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107748151 | AACAAAGAAAAAAAA[C/T]TGACAGAATTTGTCA | 10451 |
rs546807869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107588435 | GTCAAATGAGGCTAA[C/T]GTAACACTTCACACT | 10451 |
rs546824763 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107671075 | AGTGAAAAGCTATAA[C/T]GTTAGGCCTATAATG | 10451 |
rs546825496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107945310 | GAAAAACACCTACAT[A/G]TTTAATTTCAGAGCA | 10451 |
rs546832788 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107610845 | GTCTCATGTCCAAAT[A/G]TCTGATATATGCATT | 10451 |
rs546834960 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107660040 | AATCTCTCCTACAAC[G/T]GAAATGAAAATTCCT | 10451 |
rs546840526 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107689574 | GAAATGGAAGATCCA[C/T]GGGCAGAAAGTCACC | 10451 |
rs546842348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107837460 | AAAATGGCCATACTG[C/T]CCAAAGCAATTTACA | 10451 |
rs546845101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107609401 | AGAAGCTACTAGTGT[C/T]AACCAGAAGCAGTGG | 10451 |
rs546862247 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107795717 | AACATTTGCATAAGT[C/T]GTTAGGGCTTTAATA | 10451 |
rs546869196 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107639980 | CAAATGTTGGCAAGG[A/T]TAAGAGGCACCTAAA | 10451 |
rs546882301 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107623340 | TGTTTTATTTTATCT[A/G]TAATATTGTTTCTTG | 10451 |
rs546883369 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107731863 | GATTTTGACCATTAT[C/G]AAAAGGTATTCAGAA | 10451 |
rs546911061 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107793356 | TATGAGAGTTGAAAG[C/G]GTGTCTGCATTCTAT | 10451 |
rs546914184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107959586 | CCTACCTCATGGCCA[C/T]TGCCTCTCAACTCCT | 10451 |
rs546919407 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV3 | GRCh38.p7 | 1:107631049 | AGACTATATCAAGTT[C/T]GGTACAAAGACTGTT | 10451 |
rs546935365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107851166 | GAAAGAGTGAGACTC[C/T]GTCTCAAAAAAAAAA | 10451 |
rs546939906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107595758 | GCATCCAAAAAAACA[C/T]ATTAGTAATGTCAAA | 10451 |
rs546946239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107817149 | GGGGAAAGACACATA[A/T]CTGACGCATTATGAT | 10451 |
rs546954730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695858 | ATGTGCCATGGATCT[A/G]TCCATTAAAAGGTAG | 10451 |
rs546955847 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928162 | CTTATCAAAGACCAT[C/T]AAGGCGGTGCCTCTA | 10451 |
rs546955849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107870923 | TGACTTTAGTCACTC[A/G]TCTGGACAGTGGCAG | 10451 |
rs546967392 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107913848 | TTGCCCAGGCTGGAG[A/T]GAAGTGGCATGATCT | 10451 |
rs546984995 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107816383 | TAGATAATGAAAAAG[C/G]TCTCATCTAGTGCCA | 10451 |
rs546986683 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767262 | TTTCCCGATAAGCAA[C/T]TAATTTTCAGTCAGG | 10451 |
rs546990843 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107863846 | TCAAACCAGATTTCC[A/G]GTTTTGGAAACATTC | 10451 |
rs546996842 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107615145 | CCAATGAAACAGAAT[-/A]AAGAGCCCAGAAATA | 10451 |
rs547016139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107921537 | GCCTGGACACAGTAA[A/G]GTTCTGGAAAGTGGT | 10451 |
rs547020818 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107640273 | CTCCACACATGGAAC[C/G]ATAATCAGCGATAAA | 10451 |
rs547020997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755039 | TGTTCACAGTTACAG[C/T]CCCAGCCCCAAGCAA | 10451 |
rs547025151 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107943791 | TTACAGTTTGAAGTC[A/G]TGGCCTAGAGCCTTG | 10451 |
rs547033015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107734949 | CAAAATTGACCACAT[A/T]GTTGGAAGTAAAACA | 10451 |
rs547036626 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107647492 | CCTATAGTCAGTCCA[C/T]GGAATAGACAGACAG | 10451 |
rs547047469 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107587197 | CAAATGTTGAATGCA[C/T]GAAGCAATGAATGAA | 10451 |
rs547055624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107923893 | CAATGAGAAGGTGCC[A/G]TCTATAAATCAGGAA | 10451 |
rs547055918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107609768 | TAAAGATATGGAAAG[A/G]TCAGCAATACATGAA | 10451 |
rs547074658 | snp | A/G | 0.0700422 | 0.173537 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965287 | GTGGCCGAGGGCGGG[A/G]CGCGGGGGAGGGGCC | 10451 |
rs547077256 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107920736 | TCCTCCAGTGACAGG[G/T]GATCCTCCCCCTACT | 10451 |
rs547077904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910440 | ACATAAAATATTATA[C/T]GCTATTTGTTTTCAC | 10451 |
rs547080166 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107828597 | CTGTTCCACCTTCCA[C/G]AGACTGCCCACAATC | 10451 |
rs547093559 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107601019 | AGCTCAAGCTGGTAC[G/T]TCTTGCAGAGATGTG | 10451 |
rs547114631 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782195 | TGTCTTTTATTATTG[C/T]TATTCTATTATGTAT | 10451 |
rs547119995 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107871557 | AATTTTTGTTGATGT[C/T]GGTGGAGTTTGAAGT | 10451 |
rs547120462 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107870039 | TATCCACATTGATTG[A/G]CGGGCATTTGGGCTG | 10451 |
rs547132149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707255 | TAACTCTATGACCCT[A/G]AAACTGCTGCTGAGG | 10451 |
rs547133594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667620 | CACACACAAACAAAT[C/G]ACAACACAGAAAAAC | 10451 |
rs547137002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649455 | ATGACTGAGATCACT[A/G]GTTTATAAAATGGTT | 10451 |
rs547148311 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107932602 | TAATACTTTATTATG[A/G]TAAAAGGGATTTTGC | 10451 |
rs547157547 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107745756 | TGATCCAATCATCCT[A/T]TAAACAGAATTGCCA | 10451 |
rs547184510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107962302 | CACTACAGCTAGAAC[C/T]TTTCCCAAGAAAGAG | 10451 |
rs547186947 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107838163 | TAATAACCAGAATCT[A/G]TCAGGAACTTAAATG | 10451 |
rs547194306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744949 | TGCTAGTTTCCTGAG[C/G]TACAAAACGGGTATG | 10451 |
rs547195855 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107623967 | CTCTGAAATTAAATT[C/T]ACCTTCAATTTGTAT | 10451 |
rs547199462 | snp | A/C | 0.0352966 | 0.128072 | intron-variant | VAV3 | GRCh38.p7 | 1:107701054 | CTCTAATGATCAGTC[A/C]TGTTGAGCTTTTTTT | 10451 |
rs547200014 | in-del | -/A | 0.234109 | 0.249494 | intron-variant | VAV3 | GRCh38.p7 | 1:107721733 | CTGTTCCTGGGCCTG[-/A]AAAAAAAAACGTGAT | 10451 |
rs547209704 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107623954 | CTTGGTCTAGGATCT[C/G]TGAAATTAAATTTAC | 10451 |
rs547244165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107613881 | TTTTTATTTGAGACG[A/G]AGTCTCGCTCTGTCA | 10451 |
rs547253777 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107892059 | GCTTTCACTAAATAT[G/T]ACTTACTGCTAATAA | 10451 |
rs547256692 | snp | G/T | | | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897428 | AGGTGAGTATCAGGA[G/T]CAACAGGGGAGGGAA | 10451 |
rs547261187 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107706452 | AATATTAGTGCCATC[C/T]GGGATTTCTCTGCTC | 10451 |
rs547271071 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649056 | GCCTCAAAAGCCCTC[A/G]AAAAACAAACAAACA | 10451 |
rs547278294 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107752183 | GAGCCCAGAAATAAG[A/T]CCTCACATATATGGT | 10451 |
rs547281949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107578592 | TCAGGCATTAGAATT[C/T]TCTCCTTGGACTGTT | 10451 |
rs547283357 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107900075 | CTTCTTCACTTTTCA[A/G]GGAACTCAATCCTGC | 10451 |
rs547289167 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107737290 | CATTCAGGACATAGG[C/T]ATGGGCAAGGACTTC | 10451 |
rs547289826 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795957 | TTGCTAACGCCCATC[A/C]CATTAAATCCTAATT | 10451 |
rs547298444 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107860898 | ACAAAGAAGAAAAGA[C/T]TTACAGAAACATAAC | 10451 |
rs547302166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767996 | ATGATACAACTGGAA[A/G]TAGAAAGCACCAAAT | 10451 |
rs547314475 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716646 | TTTGCCAGTATTTTA[C/T]TGAGGATTTTCACAT | 10451 |
rs547315751 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107935821 | CAGCAAAGGGAAAGG[A/T]GTTCCTATTACAATG | 10451 |
rs547316343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107627590 | CTTTCAAAATCATTA[A/G]TCATTATACCCAAAT | 10451 |
rs547320320 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107710287 | ATTGTGGCAATTATG[C/T]AGTATACATAAAATG | 10451 |
rs547322005 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107739277 | CTAATCCTTTGTCAT[A/G]CATGAAATACTTTCG | 10451 |
rs547323516 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107892675 | CTACAATAAATTTGC[G/T]ACATCAATATATATT | 10451 |
rs547333424 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107649182 | GGGAGTTCTTTCTAC[A/G]TAAGGTTATTATCAC | 10451 |
rs547339240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728804 | GACAAGAAACAATAA[C/T]GCAAGCCGAGGGCGC | 10451 |
rs547339247 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963001 | ATGACAATCTTTGGT[C/T]ATCAGAAAGATTAAA | 10451 |
rs547341923 | snp | C/G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107830074 | GAAAAGTTCCTTTCA[C/G/T]CTTTTAAAATTCAGC | 10451 |
rs547347565 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107952207 | AGCAAACTAACGCAG[G/T]AACAGAAAACCAAAT | 10451 |
rs547350095 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673870 | GAGGATTATAGGTAA[C/T]TTGTCCAGAGAACTT | 10451 |
rs547356495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107946752 | ACTTCCTATGTGACC[G/T]TGAAGAAATTGCTCA | 10451 |
rs547361296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107685458 | TAGATTATTAGCTTT[C/T]TGTTATTTTAAATGT | 10451 |
rs547366940 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107703787 | TGTGTTCAAAAGTTT[C/T]ACTGATTTTGAAAGG | 10451 |
rs547380752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107813712 | CTTACTCCTTCTATC[C/T]AACTGTATGCTTGTG | 10451 |
rs547380786 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702584 | AATTACCTAGGAACA[G/T]ACACTGAGAATATAT | 10451 |
rs547383415 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107926414 | AGAAGGCTACACCAA[C/T]TGTCTCCTTCAAAGA | 10451 |
rs547386843 | snp | C/G | 0.249886 | 0.25 | intron-variant | VAV3 | GRCh38.p7 | 1:107574963 | CAGAGTTGAGTTTCT[C/G]TGTGTGTGTGTGTGT | 10451 |
rs547392637 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107882344 | TGCTATTGAAAGATC[A/G]GCCCTGAATTTGAGG | 10451 |
rs547395366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107947555 | CACTTACTCTTCACA[A/G]TACTCTGCAGTAGGA | 10451 |
rs547410986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693387 | ACACATCTTTTTTTC[A/G]TACTTCAAATGCACT | 10451 |
rs547418884 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107820506 | GATGGATAATAGTTA[A/C]AAAAATAGAGTTAGA | 10451 |
rs547424950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107692996 | GTAGTGTAGTGGGGG[A/G]AAAAGCAAATGTCCA | 10451 |
rs547425663 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107633336 | CATTAGGCATGGTTC[C/T]AGGACTCCTGCATGA | 10451 |
rs547426068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107682001 | AACAGCACTTCTCTT[A/G]TAAGTTTATTCTTCA | 10451 |
rs547438389 | in-del | -/ATTATTATT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107884444 | ATTATTATTATTATT[-/ATTATTATT]TTGAGACAGGTTCTT | 10451 |
rs547462786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107876642 | GAGGGAAGGCAGACA[A/C]TACTGACTACTTAAA | 10451 |
rs547468304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107953621 | AGCCAGAGGCAAAGA[C/G]AAGGAAACATGAAGG | 10451 |
rs547473483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107926028 | TGGCTGCCTGTAATC[C/T]CAGCACTTTGGGAAG | 10451 |
rs547475753 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107917308 | GACAGCTCACTCAGC[A/T]TTCACCACATACCAG | 10451 |
rs547491911 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597970 | TGAGGTGAGTGAACT[C/T]AGGCAAAGTCACATA | 10451 |
rs547493225 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107727177 | TCTTCAAGTATGGAT[A/G]AATTAAGTTTCAGAG | 10451 |
rs547506575 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107716308 | CATTATTGTGACCAA[A/C]CAGCCAGCCAGTAAA | 10451 |
rs547507034 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107634886 | GCTCATCATCACTTG[C/T]CATCAGAGAAATGCA | 10451 |
rs547530587 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107657361 | TAAGAAAATTCCACA[C/T]GTATTAAATCATGGC | 10451 |
rs547537588 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589459 | TGCCAGTAGAAACTG[C/G]GAGAGGGGCATGGGA | 10451 |
rs547537829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107605885 | CCAAGCATTTTGAAT[A/G]AGGGATACTCAACCT | 10451 |
rs547545979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107835724 | TGCAGGGCAAAAAAC[C/T]CCGGCCCATAGGCAC | 10451 |
rs547547840 | snp | A/C/T | | | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966744 | ATTTCCTTTCCTCAC[A/C/T]CGCATCCTTCCCTAG | 10451 |
rs547554758 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107933542 | GTAAATTTAATTGAC[A/G/T]TATGAAAATTGAATC | 10451 |
rs547568515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107805803 | TTGCTTATAGATTCT[C/T]TGTAATTTACCTGTT | 10451 |
rs547572897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728123 | GGAAAAACAGGTCCT[A/G]TTGCTAATATCCACT | 10451 |
rs547584075 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915807 | ATCTTTAGTGAGCAC[G/T]CATTATATGTGCTGT | 10451 |
rs547592313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107697495 | TTACAAACTCCAAAA[A/G]GCAAATTTAGCCAGA | 10451 |
rs547608617 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580349 | GCAAAGAAAGCGAAA[C/T]ATATTCGGGTTCTAT | 10451 |
rs547614640 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107854254 | GGCAGAGGTTGCAGT[C/T]AGCCGAGATTGTACC | 10451 |
rs547616064 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107916526 | ATCAAATAAGACATT[A/T]AAGGAAATATTAAAA | 10451 |
rs547624710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107596456 | ATGCTAAATTTTCCA[A/T]AGGTATATGGAAGAT | 10451 |
rs547626118 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709810 | TTGTCTCCCCTTCTA[A/C]CATGACTATAAGTTT | 10451 |
rs547642472 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107882157 | ATGAGTTATTTCAGT[A/C]CCAAATGAGAAATGA | 10451 |
rs547652386 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787463 | CCAGTTGCACCCCTT[A/C]GTGGGCAGAGGGAGC | 10451 |
rs547652478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794367 | CTCCCTTCATCTTGC[C/T]TTTGCCCTTTTCAGC | 10451 |
rs547662874 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107903717 | GAAAAACTCCATCTA[C/T]CAGAAATTCCTATCT | 10451 |
rs547671798 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107936070 | ACGTAGGACATTATT[A/G]CAGTTCCTAGATTTG | 10451 |
rs547676447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107861754 | GAGTGTAAATGATTC[A/G]GCACACAATCTATAA | 10451 |
rs547680763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107690522 | CAGACACGGCACTGA[G/T]GAGACTGGTACAACA | 10451 |
rs547685641 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793090 | CACACATACCAGAAT[A/C]TGTGCTGAGCATTCT | 10451 |
rs547693281 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107888840 | TACATTCTATTTTCT[C/G]TCTATATTTCTACCT | 10451 |
rs547701037 | in-del | -/A | 0.319376 | 0.240181 | intron-variant | VAV3 | GRCh38.p7 | 1:107757037 | GATAACTATTCCAGT[-/A]AAAAAAAAAAAAATC | 10451 |
rs547704408 | snp | C/T | | | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590144 | GTCAAACTTATGGCT[C/T]CAATGACAAAAGTAG | 10451 |
rs547710855 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107908723 | AAGAAAATGTAACAA[C/T]AGGGGTAAGATGTGA | 10451 |
rs547720278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107806488 | GCCAGCTTGCTTCTA[C/T]GCCACCATTTTGAAA | 10451 |
rs547724350 | in-del | -/ATT | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918705 | TATATATATATATAT[-/ATT]TTTTTTTTTTTTTGA | 10451 |
rs547737350 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107845458 | AATGAGTTTGACGAA[C/T]TGACAGAAGTAGGCT | 10451 |
rs547747694 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107778713 | GAAATATGGAGCACT[A/G]AATAAAGAAGGTAAA | 10451 |
rs547748910 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107759008 | GTCTTCTATGACAGA[G/T]GCCTCTACTCAGGTC | 10451 |
rs547763219 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107867490 | AGGAGGGCAATAGTG[C/T]TAATGATCTGGGAAT | 10451 |
rs547772414 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107772923 | GCCTACTGGATTTTA[A/G]TAAAAAATCCAGAAA | 10451 |
rs547778973 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107686806 | TATAAAAGTGCCTGT[A/G]AGAATTATTTAGTAT | 10451 |
rs547783182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107637379 | TGTAATCCTAGCACT[C/T]TGGGAGGCTGAGGAG | 10451 |
rs547795664 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107582827 | TTGTTGGACATTTGG[C/G]TTGGTTCCAAGTCTT | 10451 |
rs547803438 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107737451 | AAATTTTTGCAATCT[A/G]CCCATCTGACAAAGG | 10451 |
rs547808175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107677667 | TTCTAAAACATAACT[A/G]CTACAATAATAGAAA | 10451 |
rs547808342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107670556 | TTGTTCTTGTGCTTC[A/G]ATGGTGATTAATGAA | 10451 |
rs547815965 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107714021 | ATTTAGGAGAAATTT[A/C]GAAAACAAAAAGCTA | 10451 |
rs547817177 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107690877 | CTGCATTCATGGATA[C/T]GGCATAGAGCTGTTT | 10451 |
rs547830237 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107677024 | CAAAGGAAAAACGAT[C/G]CATAAAAACAATTAT | 10451 |
rs547831380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107869312 | ATACAACATTAGAAA[A/G]AATGAATTTTATTTC | 10451 |
rs547851208 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107738895 | ACTCAGACAAGCCGG[A/C]GACAGTAGCACAGTA | 10451 |
rs547858330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896240 | TGTTAAAAAGAAATC[A/G]ATTGATAAAGCTCTC | 10451 |
rs547868018 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107582641 | TTGTTCGATTCCCAC[A/C]TATGAGTGAGAATAT | 10451 |
rs547872445 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107765408 | TAATTCTATGTAAAT[A/T]TTTATAGCAGGCAGA | 10451 |
rs547881618 | in-del | -/TG | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107831343 | TGAGTGAATTAAAAC[-/TG]TTTTCGTGTCATTTC | 10451 |
rs547883471 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107815252 | GCCTCCATTGTAGCT[A/T]TGACCTTGACTCAAG | 10451 |
rs547883868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107835552 | CTGCTAGCTGCAGCC[C/T]CTGCCCAATGTAGCC | 10451 |
rs547900876 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107683758 | AGTTGTTGGTACCTT[A/G]TAACAGTAAGAAAAA | 10451 |
rs547901649 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107875931 | GATAGGTGTGTACTT[C/T]AGACAGAAATATGGG | 10451 |
rs547904100 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107882799 | ATTCTAAGAAATCAT[A/T]CCTTCAAATATCCCC | 10451 |
rs547910371 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107909740 | CAATGATTCCTTTAA[A/G]TATCATAATGTAATG | 10451 |
rs547926583 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107656877 | ATATAAGCCTAACTT[C/G]TGACCTCAGCATATA | 10451 |
rs547943037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732964 | CATCTCCTAGTAGGG[A/G]CTGACTGATACCTCA | 10451 |
rs547945907 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107733102 | GGAAAACAGGGTCTG[A/G]AGTGGACCTCCAGCA | 10451 |
rs547949314 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107693445 | ATTAATACAAATGAG[A/G]TGCTTCATTCAGAAA | 10451 |
rs547964546 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107702748 | TCCCATCCACGTGTA[C/T]TCCAGATCATGAAAA | 10451 |
rs547965532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107847648 | TATAAACACCTCTAC[A/G]CAAATAAACTAGAAA | 10451 |
rs547970333 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107947845 | CTCAATGACCATTCA[C/T]GGGAGCAGTCACCCT | 10451 |
rs547972193 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107878762 | CTACTGTAAAGGTAC[A/C]TGTCCCCCCTTTATA | 10451 |
rs547982139 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786657 | TTTGGTCTTTGTAAA[A/G]TACTTCAGAAAACAA | 10451 |
rs547984912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751339 | ACTTTTAAAGCATAC[C/T]TACTCTAAAAAGCTC | 10451 |
rs547988592 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107666164 | ATATTAGGATACTAA[A/G]ATGTGAACAGGTATT | 10451 |
rs547995162 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107918045 | ATACCTTTCCTATGG[A/G]AACCACAAAGCTAAC | 10451 |
rs548008298 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107771889 | TGGGCTGTCAGCCTA[C/T]GCAATGGTTAAACCA | 10451 |
rs548028035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881937 | AATCGCTCCTTTTCC[C/T]CTACCCCTTAAAAGT | 10451 |
rs548039500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107671149 | TTATCTAATCATGTT[C/T]ACGTCCTCTAGACAA | 10451 |
rs548044654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107744331 | ACTTATTACACAGTC[A/G]AGAAATCTTAGATAT | 10451 |
rs548049309 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107603780 | CAGGCAAGCCCAAAG[A/C]AATGCAGTCTATTTA | 10451 |
rs548051222 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620093 | AATTATTGTTCAACA[C/T]GGTCTTCTCTATTAA | 10451 |
rs548061420 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107881800 | GTAGCTACCACAACA[C/G]ACAAGGCATGAGTGG | 10451 |
rs548063778 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107841354 | CTGTAATAAGAAATA[C/T]GGGGAAAAAAACTAA | 10451 |
rs548074975 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769281 | AAAAACAAACACCCT[A/G]ATCAAGTCTAACTTG | 10451 |
rs548075065 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107626438 | TAACTCAGTATTTAC[A/G]GGCAAATACCTGTCA | 10451 |
rs548097017 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107648201 | TAATGGAAATAGCAC[C/T]GTCACAGCTCATATA | 10451 |
rs548101175 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107737777 | GTAAACTACTTCAAC[A/C]ATTGTGGAAGACAGT | 10451 |
rs548102174 | snp | C/T | | | synonymous-codon, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107874994 | GGCCGTGAGAAATGT[C/T]CTTATGTTCTTCAAA | 10451 |
rs548110987 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107822608 | TGCAGTAAGCCGAGA[C/T]CGTGCCACTGCACTC | 10451 |
rs548117988 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107758232 | GCCCCCTTGGAACCA[A/T]CCTCATTGCCACTAA | 10451 |
rs548124733 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107928942 | ACCCAAAGAAGACTA[C/T]CTCAAGGTATTTGAA | 10451 |
rs548132815 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793394 | CCTTTTTATACTTGT[C/T]CTAATTTCTGACATT | 10451 |
rs548139253 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107875166 | ATTCAGCAGTACTGA[A/C]CGAGCCTGCAGTCTC | 10451 |
rs548139981 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107649368 | GAAGAATATTTGCTC[C/T]TACAGAACATGGAAG | 10451 |
rs548146835 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107853627 | TCTTTTAATGTCTTT[A/T]AAAAAAAAAGTTATT | 10451 |
rs548150616 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107934668 | ACACATCAAAAGTCT[C/T]GAAAAGGAAACTCTT | 10451 |
rs548175239 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107819808 | TATAAATAACAACTG[C/T]TTTTTTCTTTTCTGA | 10451 |
rs548175297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107961189 | CTAAACTCATTGACT[A/G]TATTACCCCTACTAT | 10451 |
rs548179102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107827869 | AATATTTTATTAGTA[A/T]CTTGAATTTATTTCA | 10451 |
rs548208908 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107919209 | TTGAATGGTTATAAA[C/T]TTTTGTGGAGAAATT | 10451 |
rs548213410 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107827144 | ACCCTGAACTACCTA[A/T]GACGACATTCAGTCA | 10451 |
rs548216845 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107621722 | ATTACAAATGCCAAA[G/T]ATAGGGAATCATCTT | 10451 |
rs548223788 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107657518 | ATTGTTATACACAGG[A/G]ACTTAATCCTTTTTG | 10451 |
rs548240545 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787342 | ATGCTTCCTGCTCTC[A/C]AAAAACCAACAGTCT | 10451 |
rs548251524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107726689 | GCATAGACTACCAAC[C/T]TCGTTTCCTTTATTA | 10451 |
rs548253502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107732881 | CCCGGCATGGTGTTT[C/G]AGCTCTGAGAATGGA | 10451 |
rs548260469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107660450 | AGCTCCTATAGACAT[C/T]CATCTATTTCTTCAC | 10451 |
rs548277075 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107793946 | GCGTACTGCTGGACA[C/T]GCCAAATCCCAGAGA | 10451 |
rs548287252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590098 | GAGAGACAGCCTAGG[C/T]TCTGTTCTGGCTTCT | 10451 |
rs548307789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107861011 | TAGAAAGATAGATTA[C/T]GCTTTATTATTAGTG | 10451 |
rs548308753 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107834907 | CCTAGCTACAGGAGA[G/T]CCCATGACCCCCACA | 10451 |
rs548310967 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107937790 | CCCAATTATTAACAC[A/C]ATATAATGACTGCAT | 10451 |
rs548313765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107960373 | CTGGAGGCTCAGGAA[C/T]GAGAAACTCTTGAGC | 10451 |
rs548315582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107953105 | ATCCACTGAATTTGG[C/T]AGCAGGAACGGGAAA | 10451 |
rs548323770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709791 | CATGTGAGAAAGGAC[A/G]TGTTTGTCTCCCCTT | 10451 |
rs548323913 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107703087 | ATGGGATCATTTTAC[A/G]TTCTTCACAGATATC | 10451 |
rs548337237 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575710 | TCAAGGCCACATTTT[G/T]TCTCATCTATGAAAT | 10451 |
rs548345934 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107825625 | TGGTCTACTCCCCTA[A/C]CTGCAAATGCTTTGA | 10451 |
rs548348597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107672722 | AGGGAGTAAGCATAA[C/T]AGATAATTCTCAGAA | 10451 |
rs548348970 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771494 | TCCTGACCTCATGAT[A/C]TGCCTGCCTCGGCCT | 10451 |
rs548364697 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107751908 | ATAAAGGGCAGAGAT[A/G]TGTGATTAACACTAT | 10451 |
rs548389410 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107931882 | CATTTTATTTCAAAT[G/T]TGTGCTTTGAACATT | 10451 |
rs548392167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107811797 | AAAGGTGAACACTAA[A/G]AGGTGATAAACATCC | 10451 |
rs548392362 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107867793 | ATTCCAGACCCTTGA[A/G]GGAGGAAAAATACTC | 10451 |
rs548421171 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107823903 | AGGAAGACAGCTCTC[C/G]AAGAAACCAATTTGC | 10451 |
rs548423579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107602862 | TATGCCAATTAGCAA[C/T]CTATAACACTTTTTA | 10451 |
rs548423674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107611509 | TCTGAAATGTGATGC[A/G]AAAAATATTTCCTCT | 10451 |
rs548427047 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107818202 | AATTCAGCAGATGAT[A/G]GACACACCCAGAGGC | 10451 |
rs548450238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107595859 | CCAGCCCTGCTTAAA[C/T]ACTATTACTCAAACA | 10451 |
rs548458948 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107632617 | CTAGATGAACTTTAA[A/G]TATGTGTGCAAAAAC | 10451 |
rs548459762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107611047 | ACAGGTTGAGCATCC[C/T]TTATCTGCAATCCTT | 10451 |
rs548465336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107721461 | TGAGAAAATGAGGTA[C/T]TCCCATGTTTAGAAC | 10451 |
rs548488481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107799165 | TAGCTATGTAAATTG[C/T]GGATTTCACTTTTTA | 10451 |
rs548488979 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107777392 | CACTAAATATGTAAG[G/T]TGTCTGCTGCCAAAA | 10451 |
rs548490665 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107806402 | ACTCACTCATCCTCA[C/T]ACTGAGTTCTGGGAT | 10451 |
rs548501192 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107676969 | AGGCAGAGGAACTTC[C/G]ACGTTTCTAATACCT | 10451 |
rs548510686 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736952 | CTAGCTGACTTCAAG[A/C]TATCCTACAAGGCTA | 10451 |
rs548516036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107832743 | GCTTCAATATTCATA[C/T]TTAAGCTATGGAAAT | 10451 |
rs548525215 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107812319 | ATAATGGAAAATCCT[A/G]TAATAGACACAAGGA | 10451 |
rs548542939 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107765247 | GGGGAAACAAGCAGA[A/C]TCTTCATCTCTTTAA | 10451 |
rs548551626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107702081 | TCCCACTGCTATAAT[A/G]TAATACCTGAGACTG | 10451 |
rs548553465 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107626286 | AAAGCCAGTTGACAA[C/T]CACCCAGGGAAAATG | 10451 |
rs548586133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107630216 | TCCTTACATCATGGA[A/G]GCCTCCAGGTTAGAA | 10451 |
rs548587815 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107774195 | CCTCAGCCTCCTGGG[C/T]AGCTGGAATTACAGG | 10451 |
rs548594916 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107589408 | GACCAGCAGAGACTG[C/G]AGCGGTGCATCTATA | 10451 |
rs548595405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107902050 | CTCCATCTCAAAAAA[A/T]AAAACAAAAAAAACA | 10451 |
rs548601359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107683720 | CTAGTAAGTCTTCCA[C/T]GTGTATATCATTACA | 10451 |
rs548610502 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107791567 | GCTGAATGTTAGAAA[C/T]ATCTGTGGAGCTTTT | 10451 |
rs548617898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107771864 | AATGTTCTGAAAATG[C/T]TGCCACAGATGGGCT | 10451 |
rs548619196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915686 | CTGTGGACAGGGGCT[A/G]TGTTTTATTCTCCAG | 10451 |
rs548622481 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107907161 | AGGCCATGGACCACA[C/T]AATCGGACTCGGAAA | 10451 |
rs548656319 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107908164 | CAGGATTTTGGCTTA[C/G]GTTCTGTGGATGAAA | 10451 |
rs548657591 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107819031 | TTGTTATCTTAAATA[C/T]TAGTGATCCCTGTTT | 10451 |
rs548658405 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107779273 | TAAGTTCTACCTTGC[G/T]CAATTAATTTCAAAC | 10451 |
rs548667434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107724417 | TCAGCTGCTTCAGAC[A/C]TTCTTTTATTCAATA | 10451 |
rs548669858 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | VAV3 | GRCh38.p7 | 1:107681675 | TTTTTTTTTTTTTGA[G/T]ACAGAGTCTCGCTTT | 10451 |
rs548676663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107761817 | CTTAATAAGTATTTA[C/T]TGAACTGAATGAAAT | 10451 |
rs548679616 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107730078 | ACTTCAGTGTTTTCT[C/T]AGAGGAACATTTTAG | 10451 |
rs548693799 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593265 | ATCACATTGTACATA[C/G]TTGAAAAAATAATTG | 10451 |
rs548705158 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107957792 | AATAATAAAAACAAT[C/G]CACTGTATTTGAAAA | 10451 |
rs548706660 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107700766 | CAGTGAACATACGCA[C/T]GCATGTATCTTTATA | 10451 |
rs548710053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107957328 | TTTCTCTGGCCTTAT[C/T]TTCTGTTGAATGACT | 10451 |
rs548730169 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107853311 | GAATGGAGCTGGGAA[A/T]ATTAAATGCAATCAT | 10451 |
rs548732924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821951 | TTGCTTTTGGAGCAG[A/G]AAGTGGGCACTTTTA | 10451 |
rs548738793 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586444 | GAAGTGCTTGGATTC[C/G]ACTGAAATATGTAGA | 10451 |
rs548741812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107696850 | GGATATATCTTATCC[C/T]TTTTCCTGCCCTCCC | 10451 |
rs548748372 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107676024 | ATGGAAAAAGGACAA[A/G]GTAGGAGAGGTGGAA | 10451 |
rs548767724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107655840 | AGTCGTCAACAGGTA[C/T]ATGAAAAATTCTCAA | 10451 |
rs548768067 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107883049 | TTTCTGTTTTGATTA[C/T]TGTCCAGGCCACAAC | 10451 |
rs548772576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107829740 | GAAACTTCAATTTTT[A/G]AATCTTAAAAACAAT | 10451 |
rs548773797 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912813 | ACATCTCTCTAGCAG[A/G]TTCCTTTATGAAAAA | 10451 |
rs548775414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107687285 | CACTCTTGATATCCT[A/G]TATGTTCAAATTATG | 10451 |
rs548780584 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107678105 | TTGTCCATGGTTTCA[C/T]AGAAGCTTGAAAAAA | 10451 |
rs548785378 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107633613 | TTTGATTGGTATGGT[A/C]CCCTTCCTCTTGTAT | 10451 |
rs548788936 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107891937 | TTGAAAGGTAACCTA[C/T]CCCTTTAAACTCCAG | 10451 |
rs548795856 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107815656 | ACAGTAGTAAACTGC[C/T]TCTTTAAAGAAGATA | 10451 |
rs548798797 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107919572 | GCCCAAGCTGACACA[C/T]CTGAACTTTGGATGG | 10451 |
rs548820936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107705618 | TAATGAAACAAAATA[A/G]TTTTACCATTTATTT | 10451 |
rs548821162 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699617 | CCTTCTGTACTGCCC[A/T]AGCAGAGGTTCTCCA | 10451 |
rs548825314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107926837 | AGGCTAAAGTGCTCT[A/G]GGGCCCAACATAAAC | 10451 |
rs548829780 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107777814 | TTACATATACGGTCA[C/T]TGACCCTGACATTTC | 10451 |
rs548834322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107792400 | GCAGCCTCAAACACA[C/G]GGGCTCAAGTGATCC | 10451 |
rs548841228 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107865187 | CTTGATCTCAAAGTC[C/T]CAGGATGAGCTGAAG | 10451 |
rs548854499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107913951 | AGGCACCTGCCACCA[C/T]GCCCAGCTAATTTTT | 10451 |
rs548876129 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107795535 | TCTCCCCTCCCCCCA[A/G]GAAAAAAAATGAATG | 10451 |
rs548876904 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107662213 | ACTTATATCCCCACA[A/C]GACATGAATACAAAT | 10451 |
rs548878851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107655363 | GGCGCCAAGAACATA[C/G]AATGAGGAAAGGGCA | 10451 |
rs548887728 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107873741 | AATCTTAGAAACCAC[C/G/T]TTCTTATCCCCCCTT | 10451 |
rs548896793 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572180 | TACTGCAAGACCCAT[C/G]TTCCCTCCAGTTAAT | 10451 |
rs548903936 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107909847 | TAATCAGTGAAGAAT[-/A]ACATTAAATATTTCA | 10451 |
rs548907314 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107828918 | ACTTACCTCTGTGAT[A/G]ACACCTGCAAAATGA | 10451 |
rs548908152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107840576 | TGTCTATTCATATTT[C/T]ACAGCCTTTCTATGA | 10451 |
rs548933011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782752 | AAGGCGAAGCGTATC[C/T]GGATTTGGAATAGAC | 10451 |
rs548959617 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107955058 | GATAATCATTATAGT[-/A]AAAAAATAGTTAACA | 10451 |
rs548961210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107587001 | ATGATGACTTCTCAG[A/G]AGTGTTACAGAACGT | 10451 |
rs548963808 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107918137 | GGGTATTCATGTATG[A/T]CCAGGTCCGAACATA | 10451 |
rs548967185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107687959 | CTCTAATGGAAAAGT[A/G]CTAGAAACATGGAAC | 10451 |
rs548971430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107943142 | GATCTCCTACTCTTA[A/G]AGTCTTGGTGGCCAG | 10451 |
rs548974278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107764683 | ATGAGCCACCCTGCC[C/T]AGCTAACTAGTAAAC | 10451 |
rs548975873 | in-del | -/A | | | intron-variant | VAV3 | GRCh38.p7 | 1:107726030 | GGTTATTGCTAGACC[-/A]AAAAAAAAATTCTCT | 10451 |
rs548987332 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107934910 | GAAACAAATTCTTGC[A/G]CGACCAGGCTATCTG | 10451 |
rs548990309 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107884557 | CTCAAGTGATCCTCC[A/C]ACCTCAGCCTCTAGA | 10451 |
rs548991575 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107884464 | TATTTTGAGACAGGT[A/T]CTTTCTTGCTCTGTC | 10451 |
rs548996730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107681377 | AATCTCTAAACAATA[C/G]CCACATGAGGATCAA | 10451 |
rs548997822 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107718416 | TATACACCAATTACA[A/G]ACAAACAGAGAGCCA | 10451 |
rs549013268 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769214 | TTTATACTCCATGAA[C/T]CACTTCCCTGTAAAT | 10451 |
rs549015754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795079 | CAAATTCTTTCATCA[A/G]AGGTATTTGGGGGCC | 10451 |
rs549033988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | VAV3, MIR7852 | GRCh38.p7 | 1:107897772 | TATACTCTTCCTTCA[C/T]GTATGGTGCTAGAAT | 10451 |
rs549042118 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107946412 | AATAAAATCTACATG[C/T]CACTCAAGTCTTTGT | 10451 |
rs549049903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107768625 | TGTTGATCAGCATTA[C/T]AAACACCAAAATTGT | 10451 |
rs549051394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107837009 | GTCCTGCTGAAGCTG[C/T]TCCCAAAAAATCAAA | 10451 |
rs549051961 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776132 | TGGTTAGCACACAAA[C/T]GGAAACTCAGTAAGC | 10451 |
rs549056755 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107710436 | ATAAAAATGTATTCA[A/C]ACACATAGCTTTGTG | 10451 |
rs549069364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107665631 | CACTTTCATATGATC[A/G]GTCATATGACAAGGT | 10451 |
rs549074874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107576120 | TTTTTCATCCCCCTT[C/T]ATACTTTCAGCCCCA | 10451 |
rs549089211 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107800935 | CCCAGTGTTTTCTTC[A/G]AGTAGTTTCACAATT | 10451 |
rs549095926 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942133 | CAGTGAATTCTTCAG[C/T]ATGTTATGCTGGCAT | 10451 |
rs549098520 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593294 | TGGTAAACATTCTAC[A/G]AACATTCTAACCTAG | 10451 |
rs549101401 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107679529 | GCAGGATGCTATGAG[C/G/T]TCCACAAATATAAGA | 10451 |
rs549127330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963775 | TAACATTCTGAAAGA[C/G]AAAGAGGCTCTGAAC | 10451 |
rs549128778 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107843522 | TTAAAAATGTATGTG[C/T]GCGTGTGTGTGTGTG | 10451 |
rs549138875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107711275 | GAAATGCAGTAATAT[A/G]TGTAGCATCTCTGTC | 10451 |
rs549155077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107891308 | TCCTCTCAGATGTTA[C/T]ATCATTTTAATCAAA | 10451 |
rs549156068 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107919102 | TATAAATTTATAATT[A/T]AAAAACAAATCAATG | 10451 |
rs549164784 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107678781 | AAAAGCAATTTGAGA[C/G]ATTTGTGTTTCCCAA | 10451 |
rs549170559 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107740062 | GAGGCCAAGATGTGC[A/G]GATCACCTGAGGTCA | 10451 |
rs549194635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911921 | CTGCAAACAGCGCTG[A/G]TTTAAACAAAAATGT | 10451 |
rs549195806 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107904520 | TTCTGCACTGTGGTC[A/G]CTGTCTTTTTCCACA | 10451 |
rs549202910 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107693589 | TCCAAAAAGGGCTAA[C/T]TTGAACAAAAAGAAG | 10451 |
rs549204890 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107608454 | GCTATCAGCTCTAGA[C/T]CTCAAATTAAATTTC | 10451 |
rs549205580 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107908760 | ATAGAAAAGGAGTAA[-/G]AAAAAGCAGTTGTTT | 10451 |
rs549223368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107782346 | CCCTCCCCTACACAC[C/T]GCCTCTTTCAGAAAA | 10451 |
rs549248160 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107837107 | AAACAATGGGCAAAA[A/C]AAAACAAAACGAAAC | 10451 |
rs549269438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107650052 | TAAGACCTGAGGAGA[A/T]GACAGTAGGCATTTG | 10451 |
rs549281239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659014 | GTGTTTTAGACATGA[A/T]GTCCTTGCCCATGCC | 10451 |
rs549286726 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107739466 | GATTCAGGGAGAGTT[A/G]AGCTGGCTTCAACTT | 10451 |
rs549299591 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107835903 | CAGGTTTCTGGCAAT[C/G]TAACCTTCAGCTCAG | 10451 |
rs549300481 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107618694 | GAGACACAGAGAAAG[C/T]AAATAATCTGCCCAT | 10451 |
rs549302360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107910922 | GAGGCGGAAGTTGCA[A/G]TGGGCCGGTATCACA | 10451 |
rs549306751 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107584654 | AATGCTGACATCTGG[G/T]AAGTAGACAAATTTC | 10451 |
rs549307436 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107761088 | AAGAGAACTATTTTG[C/T]GTATGAAAATTATTT | 10451 |
rs549317570 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107878043 | AGTTTATTTATTTTA[C/T]TTTTTTGAATTTCAG | 10451 |
rs549325982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107747005 | CTGCTTCAGTCTTGC[A/G]AGTAGCTGGGACGAC | 10451 |
rs549332798 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107729944 | AAGAGCCAGCTGCTT[C/T]GTACAGATAGTGATG | 10451 |
rs549335650 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107697176 | TTTCAGAAGGTACAG[C/G]CTACTGATGGAATGA | 10451 |
rs549341843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107843007 | AAAAGTAGAGAAAAA[A/G]GACAGACAGAGAGAA | 10451 |
rs549342499 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107658592 | TCTTCCTATTTCTCC[A/G]CATCCTCTCCAGCAC | 10451 |
rs549366509 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107614064 | CTTTTTTCTTTCCAA[C/T]CCTGAACCAATACCA | 10451 |
rs549376297 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107692948 | ACTGGTCAATGTCAG[A/C]GTAAGAAGTGGAGAC | 10451 |
rs549382909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664920 | GCATGACCCAAGGTA[C/T]AGTGGCAAGAAAGAA | 10451 |
rs549393362 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107636695 | CCTCCAAGTATAGTT[G/T]CTACTGCATGTGTAT | 10451 |
rs549399973 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107753362 | TTCAGTTTTGCAAGA[C/T]GAAGTTTTGGAGACG | 10451 |
rs549404336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107621569 | TCAAATCCAATGATT[C/T]AGTGCACTTTATGTG | 10451 |
rs549404569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107642850 | TTATTAACATTAAAA[A/G]GTGTTAATACCACCA | 10451 |
rs549410892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862687 | ACTACATCTTACCCT[G/T]AAGCCAATGTGACAA | 10451 |
rs549412113 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107670823 | AATACATCATATGCT[C/T]AACCTGAGTCCATAT | 10451 |
rs549416141 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107662741 | CGCTAACGAAAGCAC[A/G]CTTTCTGTGGGCCTA | 10451 |
rs549460155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717380 | GTGAGCATTTAGTGC[C/T]ATAAATTTCCCTCTA | 10451 |
rs549463432 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107783163 | GGAAAGGTAGACAAA[G/T]GGTTCTGCAAATCTG | 10451 |
rs549464810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963078 | TCTCATCCATTGTTA[A/G]CATTCAAATAAAGGC | 10451 |
rs549477246 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963706 | AATGTGTCAGGGAGA[C/G]GGCTCTGTCCTCTCC | 10451 |
rs549492980 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107671975 | ATGCAATAACAAAAA[A/C]GATAAATTTAGACTG | 10451 |
rs549500910 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107723595 | CTATATTAGATCACA[A/G]GGCACAAAACAACTT | 10451 |
rs549503167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107941471 | CTCTAGAAGATTCGA[A/G]AACTTCTTTTGATTC | 10451 |
rs549507392 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107790832 | AACTTGGATTACAGG[A/C]ACCTGCCACCACGCC | 10451 |
rs549515408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107807318 | CTTTGCAGTTAGGCT[C/T]AGTATTTAGAACCCA | 10451 |
rs549518064 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107734285 | AGACCAGCAATGCTA[A/G]GAAGACACTCCACCA | 10451 |
rs549530344 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107607514 | CCAGTCTCTGCTAGG[C/T]TTGATCTTTCCAAAT | 10451 |
rs549543207 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | VAV3 | GRCh38.p7 | 1:107774981 | GGAGGCCAAGGTGGG[G/T]GGATTGCTTGAGCCC | 10451 |
rs549545751 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107848922 | ATAAACATTCCTATA[C/T]ACCAATCAGACAAAC | 10451 |
rs549545942 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107688018 | TTGCACTAATTCTAC[A/G]GAATTTCAGTAATTC | 10451 |
rs549549666 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107763125 | TGGGGCTTGCGGCAC[A/G]CAGCTCCCACTGAGT | 10451 |
rs549551598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107956118 | ACTGTTAACTCACTC[A/G]TAGTGCAGGAGAGAA | 10451 |
rs549561687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107918988 | TTGGGATTACAGGCA[C/T]GAGCCACCCCGCTGG | 10451 |
rs549564577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107948525 | TAACAATTTTTTCAG[C/T]ACTATAATTGTATAT | 10451 |
rs549568338 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107855883 | CAGAGAAAGGAAAAT[G/T]TGTGGAGAAAGCTGA | 10451 |
rs549573480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107828228 | TCTTGCGTTAAATAT[C/T]GAGGAAGAAGAGTCA | 10451 |
rs549575350 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107836481 | AAAAGTTTAAAAGTT[A/C]TCAAATTAACAATCT | 10451 |
rs549589088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107583784 | TGGAAGAACATTCCA[C/T]GTTCATGGGTAGGAA | 10451 |
rs549600374 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107643803 | CAAAATTCTTTTGAA[A/C]AACATGCCAGAGGGA | 10451 |
rs549605165 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107856459 | TAGCTGAAATTTCTA[A/T]CCAATATGCTGATTT | 10451 |
rs549610558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107821867 | CAAGGTCTCGTATAA[A/G]GAAAGTGATTTATTC | 10451 |
rs549623382 | in-del | -/TA | 0.0126806 | 0.0786099 | intron-variant | VAV3 | GRCh38.p7 | 1:107612130 | ATCCGTACAAAATTA[-/TA]TATATATATATATAC | 10451 |
rs549629368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635607 | CACACGTACCCTAAA[A/T]CTTAAAGTATAATAA | 10451 |
rs549637226 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107871444 | CATATCTAACCTGAA[C/G]GCCTCTGCTGACTCT | 10451 |
rs549648389 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107813668 | CATTATTAACTATAC[G/T]CACTCTACTTTGCTA | 10451 |
rs549652289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107869958 | GTTCCATCCAGGTTG[C/T]TGCAAATGCCATTAA | 10451 |
rs549658738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107642432 | CAAGAAATAACCATA[A/G]AAATGGGCAACCAGC | 10451 |
rs549659189 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107850118 | CACTTTTACACCATT[C/G]GTGGGAGTGTAAATT | 10451 |
rs549674495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107728708 | AGGCTTAACACACAC[G/T]ACTTATAAACTTGCA | 10451 |
rs549692925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107635083 | CTCAGGGATCTAGAA[A/C]TAGAAATACCATTTG | 10451 |
rs549703651 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107592998 | CCCAAGAGCTCCCTG[C/G]TATGCCTGAGTTCTC | 10451 |
rs549706341 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107934263 | CAAGACTTTCCTGGA[G/T]GTCATCTATTAATAT | 10451 |
rs549706735 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107901159 | GCTGGGGAGCTGCTA[C/T]GTCCCAGGTATTGTA | 10451 |
rs549716041 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107698981 | ATGGGGATTACAATT[C/T]GAGATGAGATTTGGG | 10451 |
rs549716649 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107717467 | GGTTTCAAAGAACAT[C/G]TTTATTTCTGCCTTC | 10451 |
rs549717487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107598604 | CCGACCTTTAAAAGC[A/G]AAGAGAAAAAGAAAC | 10451 |
rs549724648 | in-del | -/TT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107652617 | AGTATCTATCTCCTC[-/TT]GTTTTCATATATATA | 10451 |
rs549728462 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107580032 | TTGACCTTTCCTAGC[C/T]CTCTGGTAGGCATTG | 10451 |
rs549736586 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107878412 | CAGTTTTATCTTTTA[A/G]TCAGTATCTTTTAAT | 10451 |
rs549736916 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107613371 | ATTTGTATCTCATCA[C/T]TCCATTTTCTGTTTT | 10451 |
rs549744063 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV3 | GRCh38.p7 | 1:107943406 | AAAATTAAGTGAATG[C/T]GGTGAAGCCAATTTA | 10451 |
rs549744156 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107875768 | AGTGAAAGGGGCCGG[A/G]GCTAGGGTGGAGGCA | 10451 |
rs549753925 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107808078 | TAGAAACGATGCTTT[C/T]TACATACATATTTAA | 10451 |
rs549758113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107704877 | CACTTTAGAACCTAT[C/T]GGCTAGAAGGTTAGA | 10451 |
rs549762577 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842868 | CCAATGAGAGAAATA[C/T]TAACATAATATGGAA | 10451 |
rs549764854 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107575674 | AACTGTGTGGTGACC[C/T]TGCATAGGTCTCCTA | 10451 |
rs549766351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107941368 | CAGCATCTGTTGCAA[C/T]GGCTTTTTGCTGTGT | 10451 |
rs549776798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107794989 | TTTCATTTCAGCTTA[A/G]CCTCAGATGAAGTAT | 10451 |
rs549790146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107911651 | GAAAATGGGCCACCA[C/T]AGAGACTGCTGCTAG | 10451 |
rs549790361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107709945 | GAATACAATATTTTT[A/G]CAAAAAACTATAATC | 10451 |
rs549790847 | in-del | -/ACAGATACT | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107792464 | AGGTGTGCACCAGAA[-/ACAGATACT]ACTGCAGCTACCAGC | 10451 |
rs549792267 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107717269 | CTTAGTTATTTCTTG[A/C]CTTATGCTAGCTTTT | 10451 |
rs549799504 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107637086 | GCATACCTATCTAGT[C/T]GGGCTGACCAGGCAA | 10451 |
rs549818081 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107774063 | CAGACTTTTCTCTAT[A/T]TTTGCTGTTGTTGTT | 10451 |
rs549818806 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107921527 | TACACATACGGCCTG[A/G]ACACAGTAAAGTTCT | 10451 |
rs549821135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107915898 | GAAGCATGTGGTCTA[C/G]TAGGAAAATTAGACA | 10451 |
rs549824384 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107802068 | CATTATACAGATCTT[C/T]CACTTCTTTAAATTA | 10451 |
rs549830663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107905485 | CCTATACATAGTAGA[C/T]CCATGGTAACTGTTC | 10451 |
rs549838136 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107818433 | TAGGAATCACACAGA[C/T]GCAAATTCCGGAAAA | 10451 |
rs549838403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107871041 | AGTAGGAAACATTTC[C/T]AAAGAGTGAGTTAAT | 10451 |
rs549844333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107925522 | GAAGGAAATTCTGCC[A/G]TATGCTACAACATGG | 10451 |
rs549848557 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107814428 | TTTTTTCATGTTCCT[C/G]TTGGCCATTTGTGTC | 10451 |
rs549853278 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV3 | GRCh38.p7 | 1:107911051 | TCTCTCTATTCAACA[C/T]CACCAGACAAATAAA | 10451 |
rs549855647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107716745 | TATCAGGATGATGCT[A/G]GCCTCATAAAATGAG | 10451 |
rs549869221 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107591810 | GAATAAATTGCAGAC[A/C]TAATGCCCCTTATTG | 10451 |
rs549880920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107620993 | TCAGGACCTTTTGAG[A/T]GTAAATGGGTAGTGA | 10451 |
rs549885316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107821411 | CTTGGTGCTGGGCCA[A/G]TGAAGGAGGGAAAAC | 10451 |
rs549886218 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107822341 | GAACTGGAGGAATGA[A/G]AAAAAAGAGGGGAAA | 10451 |
rs549886339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107813629 | TTCAAGTCCTCTCTT[C/T]TAGCTATTTTGAAAA | 10451 |
rs549891408 | in-del | -/C | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107895342 | ATAATGGTACTTTTT[-/C]CACATTGCTTGTCAT | 10451 |
rs549899856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107877306 | CTCTCTTGGGGATTA[C/T]GCAACTGCTCTCTTG | 10451 |
rs549915966 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107650512 | CATGATGGTATTAGG[A/G]GGTGGAGCCTTTTTT | 10451 |
rs549919029 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107582959 | GGTCAAATGGTATTT[C/G]TAGTTCTAGATCCCT | 10451 |
rs549919035 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590861 | CACGGACATCTGCAA[C/T]AGCCTCCTAACTCAT | 10451 |
rs549919612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107628493 | GTTCGTTGCCTCTGA[A/T]ATCAGCATGACTAGA | 10451 |
rs549928569 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107926175 | TAATACCAGCTACTC[A/G]CGAGGCTGAGGTAGG | 10451 |
rs549931970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107751741 | CTAGGACCTCAAGGA[C/T]GAAAAGCTCTGAGTT | 10451 |
rs549954691 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107734881 | ATCTACAGAACTCTC[C/T]ACCACAAATCAACAC | 10451 |
rs549957248 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107739075 | TTTAACCAGGGTAAT[A/C/G]CTTATTTGCTGATGG | 10451 |
rs549961128 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107918064 | CACAAAGCTAACTTC[A/C]GAAGGAAATAAAACA | 10451 |
rs549965509 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107658518 | AGATCCCTGAGGAAT[C/T]GCCACACTGACTTCC | 10451 |
rs549970904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107896357 | ATCAATCTTCCAATC[A/G]GGATCATCACTGTCC | 10451 |
rs549976490 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | VAV3 | GRCh38.p7 | 1:107690447 | CAGGGTTTGGCTGCC[A/C]GGTGGCCAGCTCTTG | 10451 |
rs549977836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107693043 | GGATTAGACCTTCGC[A/G]GTGGTGTACTGTGAG | 10451 |
rs549988019 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107699000 | ATGAGATTTGGGTGC[G/T]GACACAGAGCCAAAC | 10451 |
rs549995639 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107946833 | CCTCAACTACCCAAG[A/G]GAAATAGACATTAAT | 10451 |
rs550001097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107704305 | GAAACCATCCAACTC[C/T]CTCTTGAAGACCTCT | 10451 |
rs550002036 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107586850 | AATATATATTTATTT[C/T]GAACTAATCACAGTA | 10451 |
rs550022232 | in-del | -/TTCTTGGTGTAGACGTA | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107600105 | TGCTCTATGGTGAGG[-/TTCTTGGTGTAGACGTA]TTTACTGATTCTTAA | 10451 |
rs550029708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107657912 | GAAATTGCTAACTAA[C/T]TGCTATTAGTACAGC | 10451 |
rs550044155 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107815715 | TCAATAATTACGGCA[C/T]TATTTGTTTAAAATA | 10451 |
rs550048346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107847785 | AGTAATTAATAGCTG[A/G]CCAACTAAAAAAAGC | 10451 |
rs550055852 | snp | C/T | | | intron-variant, utr-variant-5-prime | VAV3 | GRCh38.p7 | 1:107754796 | GAGCATTTCACCTGC[C/T]ACGGCTTCTGCCTGG | 10451 |
rs550057491 | snp | A/G | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787784 | AAAGAAGGTCATTGA[A/G]CAAATTTTTTCTAAA | 10451 |
rs550058350 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107706867 | GAAACTCATGTAAAT[A/G]AGTTCCAAACAGGTA | 10451 |
rs550059167 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107923577 | TGAGGAGGCCTCAGG[A/T]AACTTACAATCATGG | 10451 |
rs550069458 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787958 | CAATGACCCCACAAT[A/C]CCACTCCTCTCCTTC | 10451 |
rs550069856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107787253 | AAGTTTCTTGTATTT[A/G]CTGAACACTTCATTC | 10451 |
rs550082973 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107598151 | CTGAGGCCAGGAGTT[C/T]GAGACCAACGTGGCC | 10451 |
rs550085999 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107883007 | TAAACCAAAACCTCC[C/T]TATTCTCAGCAATTT | 10451 |
rs550086814 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107614429 | CCCTCAATCTATCCC[A/C]TCCTCTTCAAATTCC | 10451 |
rs550097009 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107745838 | TCCCTTGATTTCCCT[C/T]CACCCTCTCACCAAT | 10451 |
rs550108392 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107683832 | TTAAGTCATAGTGAC[A/G]ATGGAGAGAACAAAG | 10451 |
rs550113773 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107883638 | AGATTTTAAATTATT[A/G]GGCAATTACATTCTT | 10451 |
rs550125062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107937291 | CCCACGCATGACTAA[C/T]TGGTCCCTTCCATGC | 10451 |
rs550127891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107848291 | GCACTCCAACCTGGG[C/T]AACAGAGCAAGACTC | 10451 |
rs550146402 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107694335 | GAAATAGTAAGAGCC[-/A]AGTGAGAACTCTAAC | 10451 |
rs550149239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107597826 | AATATATAAAGTACC[C/T]AATACATGTGAAAAA | 10451 |
rs550150580 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107664122 | GCATACATTAGCTAT[A/T]ACATAATGTTTTCTA | 10451 |
rs550153997 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572579 | ATATTTCCAAAATAA[C/T]CCTATGAAATCATGA | 10451 |
rs550160939 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107660626 | CCTAGGAGATAATTT[G/T]TTGGTATTTCAGCTT | 10451 |
rs550162191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107929893 | ATCTGCAACAACATG[A/G]ACAGAACTGGAGGTC | 10451 |
rs550164612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107842435 | TTTTGTTTCAGGTGT[A/G]TCTCTTATAAACAGT | 10451 |
rs550178053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107771985 | AGCCCATCAGCCTTT[C/T]ATTAACAGTAGGAAC | 10451 |
rs550181931 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107698221 | TTTTCCACTTTACAA[C/T]GGTATGAAAGTCACA | 10451 |
rs550183084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107864874 | CCTTGAGAGCAGGGG[G/T]TCTTGACTACCTGCT | 10451 |
rs550192427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107580351 | AAAGAAAGCGAAATA[A/T]ATTCGGGTTCTATTC | 10451 |
rs550192433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107707426 | TCATCAAGTGATATA[C/T]GTAACGTGCTTAGAA | 10451 |
rs550192593 | snp | A/T | | | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107786257 | ATAAATTTAAGAAGT[A/T]TTCTATACTTACTAT | 10451 |
rs550195124 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107800840 | ATATAATCCTATTTG[A/T]CTATCTTTGCTTTGG | 10451 |
rs550196366 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107868568 | CTCAAGATCGATGAT[A/T]TTTCTGGAATCACTG | 10451 |
rs550204232 | snp | A/G | 0.00015316 | 0.00874966 | intron-variant, missense | VAV3 | GRCh38.p7 | 1:107785487 | TGCAAGGGCAATCAG[A/G]CAGCTGCATGCTAGA | 10451 |
rs550206869 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840278 | AATACATAAAAAGTT[C/G]GTGCTTCAATATGCT | 10451 |
rs550211751 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107903984 | GATCTGCAGCTGGAT[A/G]CTCTAACACTTGGTC | 10451 |
rs550212804 | snp | A/G | 0.000258374 | 0.0113631 | intron-variant | VAV3 | GRCh38.p7 | 1:107779520 | GAAAATACTAATTAG[A/G]TATGTAGTTCAGAAA | 10451 |
rs550225522 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107900883 | AAAATAGTGTCCACA[A/G]GTTATTTTTTTACTC | 10451 |
rs550229468 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571843 | TCTCTAACAGGGGGA[G/T]GTGTCCACTGAACCT | 10451 |
rs550234117 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV3 | GRCh38.p7 | 1:107955000 | AGATGAGATAATGCA[C/T]GGAAAGCTTTAGTAA | 10451 |
rs550235431 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107857844 | AGATTCCTTTTAGAT[C/T]AGCTGGAGTTCGAGA | 10451 |
rs550243756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107804377 | ACATGTTTTAATTCA[C/T]TGCTTTTTCTAATTT | 10451 |
rs550247128 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107710743 | TATGGATAGTTTATC[G/T]CCAGGATAGTTAGCG | 10451 |
rs550248154 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107627731 | GGAAACAATGTTAAG[C/T]AGTTTTAAAATTATT | 10451 |
rs550248504 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3, MIR7852 | GRCh38.p7 | 1:107897080 | ACAAGGAGCCGGAGC[A/C]GCACTGACACCTGCC | 10451 |
rs550248746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107889882 | TAAAACATTTAATTC[A/G]TTGAAATCGATTTCA | 10451 |
rs550268153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107579482 | CTAGCCTTGCAAAGT[C/T]AGTACACCGTTCAGC | 10451 |
rs550280429 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107810709 | ATACAAGCATAATCA[C/T]CCAATAGGTAATCAT | 10451 |
rs550284288 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107704816 | ACTGTCCAGGCAGAA[A/T]GCCTGGCAAAGGTTT | 10451 |
rs550284659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107803972 | TCCTGCTGAATTGAC[C/T]CCTTATATTATTAAT | 10451 |
rs550287752 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107839823 | CACAAATTGCTAATA[C/T]CAGAAATAAAGGAGA | 10451 |
rs550328540 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107667795 | CCTGATATTTTGCTA[C/T]GATTTTATTTTCTAA | 10451 |
rs550343623 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107766208 | TTTGATTTGCGATGC[A/C]AAAAAATAAGCACCA | 10451 |
rs550343940 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107938441 | GGGCTAGGGAATAGG[A/G]ATAAATTCCCAAAGA | 10451 |
rs550350883 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107797421 | GATGTAATCCCTTTC[C/T]TTAGGGAGTTATCAA | 10451 |
rs550364977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107862564 | TTGACTATTAATATA[C/T]CACCCACTGGAATTA | 10451 |
rs550394607 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107911567 | AGACAGATAAATAAA[A/C]CATAAATCAAGTCAT | 10451 |
rs550403562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107855088 | CAGGTCTGGGAATGG[C/T]ACACATTACTGCTGC | 10451 |
rs550406433 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107893823 | AGCATTAAATATGGC[A/C]TTGTTCTTCTTCACC | 10451 |
rs550415538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107777042 | TATTCTTCATGGGGA[C/T]ACAAAACAGGAACTA | 10451 |
rs550416282 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | VAV3 | GRCh38.p7 | 1:107799524 | TAAATTAATATAGTA[A/C]CTTACTTTCCACCAA | 10451 |
rs550422229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107642266 | AAGCCGGCTAAATCC[C/T]ACCAAAACCAAGTGA | 10451 |
rs550424245 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV3 | GRCh38.p7 | 1:107634553 | ATACCATTCAGGACA[C/T]AGGTATGGGCAAGGA | 10451 |
rs550429133 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107597251 | AAAACAGAAAAAAAA[A/C]CCACTTGTTTCTTCT | 10451 |
rs550444694 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107820060 | AAGAGGATTCCTCAA[A/G]AAACTAAAAATATAA | 10451 |
rs550457207 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107799507 | AAATATAGAATAATA[C/T]GTAAATTAATATAGT | 10451 |
rs550481650 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV3 | GRCh38.p7 | 1:107762968 | ATAAAGAGATTCATC[A/G]CCCTTCACCCCATGT | 10451 |
rs550484841 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107827032 | ACCTAAAAGTTAGTA[A/T]GCTGTAATAGTTTCT | 10451 |
rs550508603 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107840902 | CTGAGCAAGGGATCA[A/G]CATGTTCAGAGATGC | 10451 |
rs550518654 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107769919 | ATCTCGATTAACACA[A/G]TTTTCTTCTAATTCT | 10451 |
rs550523935 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107767719 | TACATGCGTGCATGG[G/T]GGTGGGGATGTATAA | 10451 |
rs550529154 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107738174 | AACACTTGGACGAAG[C/G]GTGGGGAACATCACA | 10451 |
rs550554855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107783888 | CCTATCTCTACTAAA[A/G]ATACAAAAAAAAAAA | 10451 |
rs550554932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107776409 | CACAGCAATGTAAGG[A/G]GGTGGTGGCAATTTT | 10451 |
rs550572364 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107679185 | AAAGAGGAAGTGACC[A/G]TCTTTGAAGATGTCT | 10451 |
rs550579531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912952 | CTTAGGATCAAGGAA[A/G]TCAACATGCCTATTT | 10451 |
rs550580549 | snp | C/T | 3.38937e-05 | 0.00411652 | intron-variant | VAV3 | GRCh38.p7 | 1:107749639 | TAAATGGTTTAGAAA[C/T]ATGGGTTATTAATTT | 10451 |
rs550594394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107816287 | GGACAAGTTACTTCA[C/T]TTCTCTGAGCCTATT | 10451 |
rs550622715 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594530 | AACTCATGAGTTTAT[C/T]TGCTGAAAAATTTAT | 10451 |
rs550633165 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107823710 | CATTGTATTTGGAGA[C/T]GGGCTTTCTAAGAAA | 10451 |
rs550635112 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107866248 | TTTGCCTCGGTCTCT[C/T]TTTCTGCCTTATGCC | 10451 |
rs550636878 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107659876 | AGAGTGGTGAGGGCT[A/C]AACTAGACCTTTTCC | 10451 |
rs550642525 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107887206 | GAGCAGTAGCCATGA[C/G]GACTGCGCTCTTACC | 10451 |
rs550643763 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107720070 | GTCGTGGGGTCGGGG[A/G]AATGGGGCAGGGATA | 10451 |
rs550648542 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107632728 | TGATAATTGAAGTGT[C/T]AGCAGTGTCTGAGTA | 10451 |
rs550661595 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107936428 | TTAGATTATAAACAA[A/G]AAATCTAAAATCAAA | 10451 |
rs550682084 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107811126 | AAGGCACAGAGAAGA[C/T]GAAAGAAATAACATT | 10451 |
rs550699100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107667012 | GCCAGCAGCTTGTAC[C/T]GCTGCCTCTGCTCTA | 10451 |
rs550700733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107951463 | AATACAAAAGCAAAA[A/C]TTGACAAATGGGATC | 10451 |
rs550704071 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107659255 | ATTTTTATGTTAAGA[C/T]ATTTTTGAAAATACC | 10451 |
rs550714261 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107666530 | ACCGTGGCTTCTGAT[C/G]CCTCACTCCCTTTCA | 10451 |
rs550717713 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107920580 | TTCTACCCAACTAGT[A/T]TGAACTCTCCAAACC | 10451 |
rs550735830 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755883 | GATATTTTTACACAG[C/G]TTAGAAGAAGGGCAA | 10451 |
rs550738477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107700991 | TTTTAATAATTGCCA[C/T]TCTGAATAGCGTGAG | 10451 |
rs550745734 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | VAV3 | GRCh38.p7 | 1:107587756 | CCACCACACCGGGCT[A/G]ATTTTTTGTATTCTT | 10451 |
rs550749901 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107775416 | AAACCCTGTCTCTAC[C/T]AAAAATAAAAAATTA | 10451 |
rs550763901 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107944004 | CTAAACACCCATCAC[A/G]AACAGCTGTGCCTGG | 10451 |
rs550781026 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107657305 | TATGAAACAAAACAA[C/T]TTAACAGCAGTTAGG | 10451 |
rs550799235 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107860066 | TAAATTGTTCAGCAA[A/T]AATAGCGGTATATAA | 10451 |
rs550803617 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107795944 | TGATCTCACCTCATT[G/T]CTAACGCCCATCCCA | 10451 |
rs550808599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107884765 | AAAAAAAAATTAAAC[A/C]ATTTTTTAAAATATA | 10451 |
rs550815190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107695243 | TGGACATTATTCTGT[A/G]AGAAATGTAAAGTAC | 10451 |
rs550823365 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107639194 | ATGAATCATAAATCT[A/T]AATGTAAAACCTAAA | 10451 |
rs550829796 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107725039 | GACAGTTATAGAGAT[A/G]ACCATAGCAATCTAG | 10451 |
rs550834059 | snp | C/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107714943 | TTTAAATATACATCT[C/G]TCACTGCATTTCAGT | 10451 |
rs550844358 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107646231 | ACAGTCATATTCCTT[A/T]AAAAATGACAAGAAA | 10451 |
rs550848213 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107865294 | AGGGAATGTGCAGAG[A/T]CAAGTAGCAAAGCCA | 10451 |
rs550855607 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107769504 | GAGAGTCTGGAGAGC[G/T]GGCCTCAAACCTCTT | 10451 |
rs550858430 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107654488 | TTCAATGTAAAATAT[G/T]TGAAATGTAGGTGAA | 10451 |
rs550860838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107942984 | GGAACTTCTGTTGGG[G/T]TATTAGAACAATGCT | 10451 |
rs550866892 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107798108 | AAAAATAAAGAGTAA[C/T]TAATAATACATACAG | 10451 |
rs550872054 | snp | A/G | 0.0142736 | 0.0832652 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965247 | CGCGCGGGTGGGAGC[A/G]CGCCGGCGGCCGGGG | 10451 |
rs550884932 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107815824 | ACAACAGTCTCCAAC[A/C]TTTTTGGTACCAGGG | 10451 |
rs550897176 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107959242 | CTCCAGCCTGGGTGA[C/T]GGAGCAAGACTCTGT | 10451 |
rs550909831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107673412 | TCTCCAACTCAGGGC[C/T]TTTCTTGGAGCTGTT | 10451 |
rs550911860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107872313 | AAGGCTATAAAAACA[C/T]TAGGTGCTGCTATCA | 10451 |
rs550921630 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107822951 | CAAAAGACAAGTAAG[C/T]AAATAAACAGGCCAT | 10451 |
rs550929403 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107736366 | TGGCAAGGGCAATCA[A/G]GCAGGAGAAAGAAAT | 10451 |
rs550932248 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107919863 | TCAATGTCCCAGAAA[C/G]AGAACTCAGAAACAT | 10451 |
rs550933602 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107730856 | ACAGTAGGTGTTCTT[A/G]CTACAAATGAGGCAG | 10451 |
rs550952088 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107600945 | GTTTTTTAAGTCCCA[C/T]AGTAACTATAACACT | 10451 |
rs550953086 | snp | A/C | | | intron-variant | VAV3 | GRCh38.p7 | 1:107626067 | CTTCTACTTAGATGG[A/C]ACTGTCCTCATCTAA | 10451 |
rs550965823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107590357 | CTGAGGCTATTTCAT[G/T]CAAGGCATGTGCAAA | 10451 |
rs550966049 | snp | A/G | | | intron-variant | VAV3 | GRCh38.p7 | 1:107751687 | GGCGGGGGGGCGCGC[A/G]CTAATTTGGTCTATA | 10451 |
rs550968141 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107736056 | GGCTGGTTCAACATA[C/T]GCAAATGAATAAACA | 10451 |
rs550975937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV3 | GRCh38.p7 | 1:107844742 | GCCCCTGTAACCACA[C/T]TTCCTCTCTAGATTC | 10451 |
rs550985607 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107834080 | GTAAAGCAGAACCAG[G/T]TGTTTTAACTACAGT | 10451 |
rs550985655 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV3 | GRCh38.p7 | 1:107718378 | AGGATACAAAATCAA[G/T]GCGCAAAAATCACAA | 10451 |
rs550998208 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107595657 | ACCATAACATGCTTT[G/T]GTTTGCATGCTAATC | 10451 |
rs551003149 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107831195 | AATATTAGGACTTTT[C/G]AGTATAGTCTTTTAA | 10451 |
rs551016287 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107680749 | GCTCACAACAACAAC[A/G]TAAGGTAGGTCCTCT | 10451 |
rs551018171 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107950452 | CTAAGCGAGAGTTAG[A/G]GATTCAGGGTGTCTG | 10451 |
rs551020244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107745076 | TTTTGAACATTGCTA[C/T]AGGCAGTTATATCCA | 10451 |
rs551021113 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107618526 | AGGTTGGTGCAAAAG[C/T]AATTGTGGTTTTTAT | 10451 |
rs551032204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107652707 | AATGATACAAATATT[C/T]AGTTATTATTGGTAT | 10451 |
rs551038294 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV3 | GRCh38.p7 | 1:107616454 | GTGGAAGGTGGGAGG[A/C]GGGTGAGGATCTAAA | 10451 |
rs551048890 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107739552 | AACTGATGGTGCCGG[C/T]ATGGATTCTGCACCC | 10451 |
rs551053570 | snp | A/G | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107950542 | TGAGGCACTGCAAAG[A/G]GGTGAATGAAAGCAG | 10451 |
rs551053662 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107809937 | TTTTAAGAATAGTTG[A/C]GCTACAGCATAACTT | 10451 |
rs551071764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | VAV3 | GRCh38.p7 | 1:107755828 | ACTAGGTCGGAAGAA[C/T]AGAAATTCCAAGCAC | 10451 |
rs551076164 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV3 | GRCh38.p7 | 1:107587128 | TTAAGCTGTATTGTA[C/T]GTAACACTTGAGACG | 10451 |
rs551089903 | snp | C/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107904532 | GTCACTGTCTTTTTC[C/T]ACAGTCTTCAGATAA | 10451 |
rs551093322 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107928112 | GGGAAGAGAACAAAA[C/G]CCTCAGCCTGGTGGT | 10451 |
rs551103702 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV3 | GRCh38.p7 | 1:107740010 | AATGCTTCTTGGCTG[C/G]GCATGGTGGCTCACG | 10451 |
rs551111567 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107712908 | GTGTATTACCACAGA[A/C]GGATTTTCTACAGAA | 10451 |
rs551112917 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107594345 | GTGTTAGGTGTTTAA[C/T]ATATATCTGTTTAAC | 10451 |
rs551113012 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107586604 | ATTGGAGTGCATCTA[A/T]CAGAGGGTGGTGAAG | 10451 |
rs551128348 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107623179 | TTGTTCTATTTCTAG[A/C]TCTGCTATAAAAAGA | 10451 |
rs551159872 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV3 | GRCh38.p7 | 1:107912891 | ACACTTTTTCCACAA[C/T]CACACTTTCCACAGC | 10451 |