SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8458 | snp | C/T | 0.498415 | 0.0281103 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571234 | AGCCCTCGTGTAATA[C/T]GGTGAATTAGAGTGG | 10451 |
rs8676 | snp | C/T | 0.498415 | 0.0281103 | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107571243 | CCTGTATGCAGCCCT[C/T]GTGTAATACGGTGAA | 10451 |
rs76592 | snp | C/G | 0.276267 | 0.248616 | intron-variant | VAV3 | GRCh38.p7 | 1:107939571 | agacatgatgggatg[C/G]aaaaccaaaaaacac | 10451 |
rs173185 | snp | G/T | 0.111928 | 0.208413 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107963369 | CTCTGAAGGGGTACC[G/T]AGAGGTAGCAATCAC | 10451 |
rs189375 | snp | G/T | 0.438386 | 0.164349 | intron-variant | VAV3 | GRCh38.p7 | 1:107960760 | tcttttttccaaaca[G/T]tgacattcctgtgtt | 10451 |
rs191503 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107866823 | ttttttttttttttt[G/T]gagatggagtctcgc | 10451 |
rs345266 | snp | A/T | 0.345037 | 0.231231 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966843 | AATAAATCATACTAA[A/T]CTCTACATACCTTTA | 10451 |
rs345267 | snp | C/T | 0.344592 | 0.231414 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966808 | AATAGCACGACATTT[C/T]CTAGGCCATAATTTT | 10451 |
rs345268 | snp | A/G | 0.344815 | 0.231323 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107966374 | GGCGTGGTGGCACGC[A/G]CCTGTAGTCCCAGCT | 10451 |
rs345269 | snp | A/G | 0.493107 | 0.0583 | upstream-variant-2KB, intron-variant | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107965014 | GGGAGCAGGAGCCGC[A/G]GCTGACGGGTCGCGG | 10451 |
rs345270 | snp | A/T | 0.186105 | 0.241697 | intron-variant | VAV3 | GRCh38.p7 | 1:107955644 | TCATTTGTCTACTTG[A/T]AGATTCAGTTCAAGA | 10451 |
rs345271 | snp | A/G | 0.482159 | 0.0927485 | intron-variant | VAV3 | GRCh38.p7 | 1:107955523 | TTCTTGCTGTTTTGC[A/G]GTTTTTTTTCCTTAT | 10451 |
rs345272 | snp | A/C | 0.399253 | 0.200558 | intron-variant | VAV3 | GRCh38.p7 | 1:107955210 | ACTCTCAGAAAGTGA[A/C]TAAACCTGTCTATCT | 10451 |
rs345273 | snp | A/G | 0.186105 | 0.241697 | intron-variant | VAV3 | GRCh38.p7 | 1:107954362 | TAGCTGTTCCTTTTT[A/G]GCCTTTTAATACTGT | 10451 |
rs345274 | snp | C/T | 0.497558 | 0.0348586 | intron-variant | VAV3 | GRCh38.p7 | 1:107952673 | GGATGGGAAGGGAGC[C/T]GTTTGGGTTAGAGTG | 10451 |
rs345275 | snp | A/T | 0.388587 | 0.208071 | intron-variant | VAV3 | GRCh38.p7 | 1:107951181 | AGTAGAGAGAGAGTT[A/T]TGTGAGATGAAGAAT | 10451 |
rs345276 | snp | C/T | 0.406814 | 0.194704 | intron-variant | VAV3 | GRCh38.p7 | 1:107950112 | TTGTGGTTTCCAGAA[C/T]CCAGGGGTGTGCTTG | 10451 |
rs345277 | snp | A/G | 0.436123 | 0.166908 | intron-variant | VAV3 | GRCh38.p7 | 1:107950090 | GTGTGCTTGGAGAGC[A/G]TTATCGATGAACCAG | 10451 |
rs345278 | snp | A/G | 0.210909 | 0.246925 | intron-variant | VAV3 | GRCh38.p7 | 1:107949351 | TGCACTCCAGCCTGG[A/G]CAGCAAAGCAAGACC | 10451 |
rs345279 | snp | G/T | 0.116138 | 0.211142 | intron-variant | VAV3 | GRCh38.p7 | 1:107948703 | GGCACATACCACCAC[G/T]CCTAGCTAATTTTGT | 10451 |
rs345280 | snp | A/G | 0.116488 | 0.211364 | intron-variant | VAV3 | GRCh38.p7 | 1:107948664 | TAGAGATGGGATTTC[A/G]CCATGTTGGCTAGGC | 10451 |
rs345281 | snp | A/G | 0.492435 | 0.0610346 | intron-variant | VAV3 | GRCh38.p7 | 1:107947953 | CATGTATGTTTAGGC[A/G]TCACCATAAGTTATT | 10451 |
rs345282 | snp | C/T | 0.097727 | 0.198275 | intron-variant | VAV3 | GRCh38.p7 | 1:107947837 | TGCTCCCATGAATGG[C/T]CATTGAGTGATTATT | 10451 |
rs345283 | snp | A/C | 0.116138 | 0.211142 | intron-variant | VAV3 | GRCh38.p7 | 1:107947464 | TGTGAGATTCTTTCC[A/C]TTCTCCTGTCCCACA | 10451 |
rs345284 | snp | A/G | 0.116138 | 0.211142 | intron-variant | VAV3 | GRCh38.p7 | 1:107946380 | CAATCTCAGTCACTT[A/G]TTTGTGAAATGACTT | 10451 |
rs345285 | snp | A/G | 0.116138 | 0.211142 | intron-variant | VAV3 | GRCh38.p7 | 1:107945594 | tcagatagtccgctc[A/G]tctcaacctctcaaa | 10451 |
rs345286 | snp | A/G | 0.492337 | 0.0614248 | intron-variant | VAV3 | GRCh38.p7 | 1:107944812 | TCGAGACCAGCCTGG[A/G]CAACATGGTGAAACC | 10451 |
rs345287 | snp | C/G | 0.0700422 | 0.173537 | intron-variant | VAV3 | GRCh38.p7 | 1:107944752 | CTGGGTGTGGTAGTG[C/G]ACGCCAATAGTCCCA | 10451 |
rs345288 | snp | G/T | 0.231482 | 0.249313 | intron-variant | VAV3 | GRCh38.p7 | 1:107878436 | gaataaaggcaaaag[G/T]atttttagattaaaa | 10451 |
rs345289 | snp | C/T | 0.356597 | 0.226135 | intron-variant | VAV3 | GRCh38.p7 | 1:107880520 | acatgagccaccgca[C/T]ctggccTCCAGTTTT | 10451 |
rs345290 | snp | A/G | 0.235564 | 0.249583 | intron-variant | VAV3 | GRCh38.p7 | 1:107882122 | CAATAAGCTGTAGAG[A/G]TTTTTCCTCTTCCAT | 10451 |
rs345291 | snp | C/T | 0.121369 | 0.214369 | intron-variant | VAV3 | GRCh38.p7 | 1:107882130 | TCATCTCACAATAAG[C/T]TGTAGAGATTTTTCC | 10451 |
rs345292 | snp | A/G | 0.406814 | 0.194704 | intron-variant | VAV3 | GRCh38.p7 | 1:107882433 | AGGCACAGAAGAGAC[A/G]ACCATGAAACCGATT | 10451 |
rs345293 | snp | C/T | 0.404559 | 0.196498 | intron-variant | VAV3 | GRCh38.p7 | 1:107882614 | TGGAGTTCCCTATTT[C/T]TGTCCCTTTCACCAT | 10451 |
rs345294 | snp | G/T | 0.232359 | 0.249377 | intron-variant | VAV3 | GRCh38.p7 | 1:107883971 | AAAAACTGAATACCT[G/T]GGAAGTGCAGAGGTC | 10451 |
rs345295 | snp | C/T | 0.399968 | 0.200024 | intron-variant | VAV3 | GRCh38.p7 | 1:107884121 | TAGCTCAAAGCAACC[C/T]AGAGATGGGGCCCAG | 10451 |
rs345296 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | VAV3 | GRCh38.p7 | 1:107884463 | ttattTTGAGAcagG[G/T]TCTTtcttgctctgt | 10451 |
rs345297 | snp | C/T | 0.499121 | 0.020948 | intron-variant | VAV3 | GRCh38.p7 | 1:107893625 | AGTGAATAAGTCTCA[C/T]GAGATCTGATGGTTT | 10451 |
rs345298 | snp | A/G | 0.388964 | 0.20782 | intron-variant | VAV3 | GRCh38.p7 | 1:107893935 | TTCTTGCACAGAGGT[A/G]GCCCTGACATTTATT | 10451 |
rs345299 | snp | A/C | 0.350764 | 0.228794 | intron-variant | VAV3 | GRCh38.p7 | 1:107905511 | TGTTCATGGAAGCCA[A/C]TGCTAAAGACCTCTG | 10451 |
rs345300 | snp | G/T | 0.44651 | 0.154543 | intron-variant | VAV3 | GRCh38.p7 | 1:107939902 | CCACATTCTCTACCT[G/T]TCCTGTCTTACTCTT | 10451 |
rs345302 | snp | A/G | 0.494651 | 0.0514399 | intron-variant | VAV3 | GRCh38.p7 | 1:107934185 | TCCTTATTCTAAAGG[A/G]TATAATTATTTAAAG | 10451 |
rs345303 | snp | A/G | 0.492287 | 0.0616198 | intron-variant | VAV3 | GRCh38.p7 | 1:107928221 | gctgtatctgcatta[A/G]gaggcaccccaaacc | 10451 |
rs345304 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | VAV3 | GRCh38.p7 | 1:107927697 | ttccctcccctttcc[A/G]caggcagaggagcct | 10451 |
rs345305 | snp | G/T | 0.0962929 | 0.197165 | intron-variant | VAV3 | GRCh38.p7 | 1:107925194 | acttctatcttgacc[G/T]tcaacgctaagatta | 10451 |
rs345306 | snp | A/C | 0.452473 | 0.146644 | intron-variant | VAV3 | GRCh38.p7 | 1:107924764 | GGAACATATGGTCAC[A/C]GTTTTTTTTCCCCCA | 10451 |
rs345307 | snp | A/G | 0.445987 | 0.155207 | intron-variant | VAV3 | GRCh38.p7 | 1:107916784 | AGGCAGTGAGTGAAT[A/G]AATGAATTAATACGA | 10451 |
rs345308 | snp | A/G | 0.406986 | 0.194565 | intron-variant | VAV3 | GRCh38.p7 | 1:107916985 | AGTGACTGGAAATTC[A/G]GGCAGAGGAGACCAA | 10451 |
rs345309 | snp | C/T | 0.492823 | 0.0594727 | intron-variant | VAV3 | GRCh38.p7 | 1:107917024 | TAGAAATGTTGGTGA[C/T]GATCAGATTGTCCAA | 10451 |
rs345310 | snp | C/T | 0.335559 | 0.234904 | intron-variant | VAV3 | GRCh38.p7 | 1:107917102 | TGCAGAAAGTCATCA[C/T]GGTTTCTGAAGAGAA | 10451 |
rs345311 | snp | A/G | 0.492237 | 0.0618148 | intron-variant | VAV3 | GRCh38.p7 | 1:107918798 | GAATTGCTTGAACTC[A/G]GGAGGCAGAGGTTGC | 10451 |
rs345312 | snp | A/G | 0.298651 | 0.24522 | intron-variant | VAV3 | GRCh38.p7 | 1:107918852 | TGGGCATGGTGGTGG[A/G]TGTCTGTAATCCCAG | 10451 |
rs345313 | snp | C/T | 0.299158 | 0.245119 | intron-variant | VAV3 | GRCh38.p7 | 1:107919840 | GACATTGATTCTTTT[C/T]TTTAATTAATTTTCT | 10451 |
rs345314 | snp | A/G | 0.299158 | 0.245119 | intron-variant | VAV3 | GRCh38.p7 | 1:107920222 | GCCAGTACTGTTCCC[A/G]TTTTATCACATGCTA | 10451 |
rs345315 | snp | A/C | 0.122064 | 0.214785 | intron-variant | VAV3 | GRCh38.p7 | 1:107873762 | CTTGGAAAGCTGTAC[A/C]AAAGGAAGGGGGGAT | 10451 |
rs345316 | snp | A/G | 0.226188 | 0.248863 | intron-variant | VAV3 | GRCh38.p7 | 1:107873495 | TTTATCCTTCCGCCT[A/G]TTCCTCCTGCACCTT | 10451 |
rs345317 | snp | C/T | 0.121717 | 0.214577 | intron-variant | VAV3 | GRCh38.p7 | 1:107872692 | TCACATAGCACATAA[C/T]GTGTACTTTGCATAT | 10451 |
rs345318 | snp | C/G | 0.336702 | 0.234484 | intron-variant | VAV3 | GRCh38.p7 | 1:107871345 | CTGCTGAGGTCTGGT[C/G]GGGGGAGAGGGGGGG | 10451 |
rs345319 | snp | A/G | 0.124491 | 0.216211 | intron-variant | VAV3 | GRCh38.p7 | 1:107871096 | GTTTCCGTACTGTAT[A/G]TAAAGAATTTTCCAT | 10451 |
rs345320 | snp | A/G | 0.226188 | 0.248863 | intron-variant | VAV3 | GRCh38.p7 | 1:107869758 | aattgggtttagtgt[A/G]tactgctcgggtgat | 10451 |
rs345321 | snp | G/T | 0.0850919 | 0.187897 | intron-variant | VAV3 | GRCh38.p7 | 1:107869742 | tactgctcgggtgat[G/T]ggtgcaccaaaatct | 10451 |
rs345322 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | VAV3 | GRCh38.p7 | 1:107869702 | actaaataacttact[C/T]atgtaaccaaatacc | 10451 |
rs345323 | snp | A/G | 0.103794 | 0.20279 | intron-variant | VAV3 | GRCh38.p7 | 1:107864576 | gagtgcagtggtgca[A/G]tcttggctcactgca | 10451 |
rs380677 | snp | G/T | 0.293037 | 0.246268 | intron-variant | VAV3 | GRCh38.p7 | 1:107958758 | ggagggataacatta[G/T]gagaaatacctaacg | 10451 |
rs385585 | snp | A/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107929307 | tgttctagggcataa[A/T]ttttttttttttttt | 10451 |
rs394635 | snp | C/T | 0.116138 | 0.211142 | intron-variant | VAV3 | GRCh38.p7 | 1:107943906 | TTTGGGTTTTGTGGG[C/T]ACAGCTTGGACTCGT | 10451 |
rs409129 | snp | A/G | 0.399611 | 0.200291 | intron-variant | VAV3 | GRCh38.p7 | 1:107888750 | AGATATGAGCCACTG[A/G]GCCGGGCCTACCCTG | 10451 |
rs411926 | snp | G/T | 0 | 0 | intron-variant | VAV3 | GRCh38.p7 | 1:107938527 | AGCTCTTCCCTCCAT[G/T]CCTGCTTCCTCTTCC | 10451 |
rs423488 | snp | A/G | 0.225893 | 0.248835 | intron-variant | VAV3 | GRCh38.p7 | 1:107873798 | GGCACCAGCCTTCTC[A/G]GGCATCAGGCTGCCT | 10451 |
rs436666 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | VAV3 | GRCh38.p7 | 1:107958847 | agatatatctatata[C/T]gaagaatgagaacat | 10451 |
rs439278 | snp | C/T | 0.364817 | 0.222075 | intron-variant | VAV3 | GRCh38.p7 | 1:107873799 | AGGCACCAGCCTTCT[C/T]AGGCATCAGGCTGCC | 10451 |
rs445581 | snp | G/T | | | intron-variant | VAV3 | GRCh38.p7 | 1:107939007 | gaaagtaacagaaaa[G/T]ggaagtgaggtacag | 10451 |
rs451046 | snp | A/T | 0.396727 | 0.202413 | intron-variant | VAV3 | GRCh38.p7 | 1:107890682 | GCCTTCTTTGAGTCA[A/T]ATGTTCACAGTGAAA | 10451 |
rs496737 | snp | A/G | 0.116138 | 0.211142 | intron-variant | VAV3 | GRCh38.p7 | 1:107945605 | CGAGCTTGACCTCAG[A/G]TAGTCCGCTCGTCTC | 10451 |
rs719122 | snp | G/T | 0.0689305 | 0.172377 | intron-variant | VAV3 | GRCh38.p7 | 1:107893693 | TGTGGGAGTGACCTG[G/T]TGGGAGGTAATTGAA | 10451 |
rs746302 | snp | C/T | 0.31503 | 0.241394 | intron-variant | VAV3 | GRCh38.p7 | 1:107865103 | ATCAAAACATGAAGG[C/T]TCTGAGAGGCTGAGC | 10451 |
rs922115 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | VAV3, VAV3-AS1 | GRCh38.p7 | 1:107962572 | TAATGACAACCTGCA[A/T]GATACAAACTCATCG | 10451 |
rs943755 | snp | A/G | 0.435263 | 0.167862 | intron-variant | VAV3 | GRCh38.p7 | 1:107606607 | CAAAAAGTCAGAGAT[A/G]GATAATATGAGAGAA | 10451 |
rs943757 | snp | A/G | 0.440884 | 0.161442 | intron-variant | VAV3 | GRCh38.p7 | 1:107603918 | ACTTGGGAGGCTGAG[A/G]CACAGGCCTCCCTTG | 10451 |
rs943758 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | VAV3 | GRCh38.p7 | 1:107600481 | TGCATATGTGTTTTC[G/T]TCTCCATATCTGGGC | 10451 |
rs1020812 | snp | A/G | 0.396546 | 0.202545 | intron-variant | VAV3 | GRCh38.p7 | 1:107942010 | TAAGGGGAGGCAGGA[A/G]AAGATGAGGGGTATT | 10451 |
rs1023212 | snp | C/T | 0.318656 | 0.240388 | intron-variant | VAV3 | GRCh38.p7 | 1:107861418 | GAAGCAGCAGAAAAA[C/T]TAGAATTTATTGGCT | 10451 |
rs1075564 | snp | C/T | 0.0854556 | 0.188216 | intron-variant | VAV3 | GRCh38.p7 | 1:107865371 | CTTAAAATCTGAAAT[C/T]ATGTGCTTTATCCAG | 10451 |
rs1079061 | snp | C/T | 0.461592 | 0.133149 | intron-variant | VAV3 | GRCh38.p7 | 1:107865439 | CTTTAGTCCCTTGTC[C/T]GCGGTGACTCAATTC | 10451 |
rs1113981 | snp | A/G | 0.447162 | 0.153712 | intron-variant | VAV3 | GRCh38.p7 | 1:107837008 | agtcctgctgaagct[A/G]ttcccaaaaaatcaa | 10451 |
rs1113982 | snp | A/G | 0.27278 | 0.24896 | intron-variant | VAV3 | GRCh38.p7 | 1:107837118 | AAAAAAAAACAAAAC[A/G]AAACAAAACTTCAAG | 10451 |
rs1129409 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | VAV3 | GRCh38.p7 | 1:107572002 | GNTCTGACAAGACTG[A/C]GCGAGTTCCATGNTG | 10451 |
rs1154941 | snp | A/G | 0.229429 | 0.249152 | intron-variant | VAV3 | GRCh38.p7 | 1:107939774 | CTTCCTTCCTTCCCC[A/G]TTTTTAATCTGCTCC | 10451 |
rs1328198 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | VAV3 | GRCh38.p7 | 1:107593851 | CTTATTCTAACACAG[C/T]ACTTTCCTATATTTC | 10451 |
rs1328199 | snp | A/G | 0.34146 | 0.23267 | intron-variant | VAV3 | GRCh38.p7 | 1:107585273 | TAGTGGCCTGGAACA[A/G]CACGTAGCCATATAG | 10451 |
rs1328204 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV3 | GRCh38.p7 | 1:107614823 | TGAATAAGGCATAAA[A/G]ATGAGCACTTGAAGT | 10451 |
rs1328205 | snp | A/C | 0.435119 | 0.16802 | intron-variant | VAV3 | GRCh38.p7 | 1:107614788 | TTTTAGGGATAGTCT[A/C]GCACAAAGTAGGCAT | 10451 |
rs1328206 | snp | A/G | 0.443195 | 0.158668 | intron-variant | VAV3 | GRCh38.p7 | 1:107613419 | GAAGAAATTGCTCAA[A/G]GAGCAGTTAAGAGAG | 10451 |
rs1328207 | snp | C/T | 0.113685 | 0.209567 | intron-variant | VAV3 | GRCh38.p7 | 1:107611181 | TAAGCACTGACATGA[C/T]GCTCAAAGGAAATGC | 10451 |
rs1328208 | snp | A/T | 0.443195 | 0.158668 | intron-variant | VAV3 | GRCh38.p7 | 1:107609710 | AGTGCCCAGTGCCCT[A/T]GACTGATAATTTAAA | 10451 |
rs1328209 | snp | A/C | 0.443195 | 0.158668 | intron-variant | VAV3 | GRCh38.p7 | 1:107609609 | AGAGAGAAAAATATG[A/C]TTTCATTGTCTAAAA | 10451 |
rs1332684 | snp | A/G | 0.173965 | 0.238157 | intron-variant | VAV3 | GRCh38.p7 | 1:107871608 | TTCAGTGCTACCTTT[A/G]TTCTTAGAATTGAGC | 10451 |
rs1360564 | snp | A/G | 0.470715 | 0.117409 | intron-variant | VAV3 | GRCh38.p7 | 1:107869172 | GGTTTCATCAATTAT[A/G]TCCCATGCCTTTGAC | 10451 |
rs1360565 | snp | C/T | 0.466927 | 0.124269 | intron-variant | VAV3 | GRCh38.p7 | 1:107869066 | TTTCTCTCTTCCTGA[C/T]ACAGAAGAGTGTAGA | 10451 |
rs1380445 | snp | A/C | 0.448195 | 0.152377 | intron-variant | VAV3 | GRCh38.p7 | 1:107843782 | ACAACTGAACAGGCA[A/C]AAGACTCCCCCAAAA | 10451 |