SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs138906534 | in-del | -/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856876 | TTTAGGAGGTAATGG[-/GT]GTGTGTGTGTGTGTG | 7409 |
rs138914832 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6806620 | CTTGACCAACACAGC[A/G]GAGAGTAAATCACTG | 7409 |
rs138934340 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | VAV1 | GRCh38.p7 | 19:6789690 | GCAACCTCCGCATCA[C/T]GGGTTCGAGTGATTC | 7409 |
rs138936512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841205 | CAGGCATGAGCCACC[A/G]TGCTGGGCAATTTTC | 7409 |
rs138939156 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | VAV1 | GRCh38.p7 | 19:6847333 | CCTCCCGCAGCCCCC[A/G]GGAACCAAGGGTCTC | 7409 |
rs138966618 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | VAV1 | GRCh38.p7 | 19:6786367 | CCCGGGAGGCTGAGA[C/T]GGGAGGATCGCTTGA | 7409 |
rs138990400 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799877 | AAAAAGGAAAGAAAA[A/G]AAAACAGAATCAAGC | 7409 |
rs139010326 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803103 | TGGGACGGTTCTTTG[C/T]TTTGCCCAGGAAAGA | 7409 |
rs139047554 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6833414 | GATCTTCTGCTTCTC[C/T]GTCACTCTCCTGATC | 7409 |
rs139062430 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | VAV1 | GRCh38.p7 | 19:6781991 | AAAATAATTACTTAA[C/G]CTATTGGATCCCTGA | 7409 |
rs139156511 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | VAV1 | GRCh38.p7 | 19:6846017 | ATATTACATATTTAC[A/G]TTTACATTATGTTAG | 7409 |
rs139258568 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | VAV1 | GRCh38.p7 | 19:6795840 | AGGCGCGTGCCACCG[C/T]GCCCAGCTAATTTTT | 7409 |
rs139302836 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6803864 | GCCACTGCTCCCAGC[A/G]CAGACAATGGAATAT | 7409 |
rs139303999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6823683 | CTCTGGGTCTCCTCT[C/T]GCTACTTTCTTCCTC | 7409 |
rs139322985 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6795166 | AAGAAGCCATACCCT[C/G]GCTTCTCTCTTCCTA | 7409 |
rs139408792 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819824 | TGAACCTGTTGGGAC[A/G]TTGGATGAGCCAATA | 7409 |
rs139409199 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6778503 | CCACACCTGGGTTCA[A/G]ATTCTGGTACCACCA | 7409 |
rs139423886 | snp | C/T | 0.021333 | 0.101051 | intron-variant | VAV1 | GRCh38.p7 | 19:6839526 | GCCTGCCTCGGCCTC[C/T]CAAAGTGCTGGGATT | 7409 |
rs139447179 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6853268 | ATAATTTAATTAATT[A/T]ATTTATTTATTTTTT | 7409 |
rs139448507 | snp | A/G | 0.0748431 | 0.178382 | intron-variant | VAV1 | GRCh38.p7 | 19:6787862 | CAGGTGGATCACGAG[A/G]TCAGGAGATCGAGAC | 7409 |
rs139458004 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | VAV1 | GRCh38.p7 | 19:6790051 | GCCATGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 7409 |
rs139461610 | in-del | -/ATTTATTTATTTATTTATTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787574 | GACCAACTACTCCAG[-/ATTTATTTATTTATTTATTT]ATTTATTTATTTATT | 7409 |
rs139547177 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | VAV1 | GRCh38.p7 | 19:6817445 | GAGGAGAGTGTTAAT[A/G]TGCAGATTCCCAGGC | 7409 |
rs139549037 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | VAV1 | GRCh38.p7 | 19:6788410 | CTGAGTCTTGCTCTG[C/T]TGCCCAGGCTGGAGT | 7409 |
rs139553703 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6790477 | TGTCTGCAGAGCTGT[A/G]CTCCCTCTGGGGGCT | 7409 |
rs139589881 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6815342 | AGACAGTGTCTCTCC[A/G]TGTTGCTCAGGCTGG | 7409 |
rs139682102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814029 | CGTGCCACTCCACTC[C/T]GGCCTGGGTGACAGA | 7409 |
rs139696954 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6781584 | TTGTTGCACTTTCTA[C/G]AACTACTGACCTTTT | 7409 |
rs139700395 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV1 | GRCh38.p7 | 19:6820139 | GCCTGGGCAACATAG[C/T]GAGACCTCGTCTCTA | 7409 |
rs139722302 | in-del | -/A/ATCA/ATCCA/ATCCATCA | 0.0193772 | 0.0965046 | intron-variant | VAV1 | GRCh38.p7 | 19:6776117 | TCCATCCATCCATCC[-/A/ATCA/ATCCA/ATCCATCA]ATCCATCTGCTCATC | 7409 |
rs139752709 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | VAV1 | GRCh38.p7 | 19:6808038 | AAAAAAAAGGCCGGG[C/T]GCGGTGGCTCAAGCC | 7409 |
rs139773795 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV1 | GRCh38.p7 | 19:6805020 | ACAGGTGTGAGCCAC[C/T]GCCCCCCGGCCCATA | 7409 |
rs139820534 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6834982 | CAGGAGTTCAAGGTT[A/G]CAGTGAGCCATGATC | 7409 |
rs139881196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777379 | TTGTTGAGGAGCCTG[C/T]ATTCTAGTGGGGGAG | 7409 |
rs139907459 | in-del | -/TATC | 0.499992 | 0.00199679 | intron-variant | VAV1 | GRCh38.p7 | 19:6838214 | TATCTACCCATCTAT[-/TATC]TATCTATCTATATCA | 7409 |
rs139934636 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6855982 | GGCTCTTGGGATTCA[C/G]TGACAAATAATACAG | 7409 |
rs139966812 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | VAV1 | GRCh38.p7 | 19:6795808 | CCTGTCTCAGCCTCC[C/T]GAGCAGCTGGGACTA | 7409 |
rs139970377 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6849671 | CCCCTGCTTATAAGT[A/G]AGAACATGTGGTGTT | 7409 |
rs139972688 | snp | A/C/G | 0.0441359 | 0.141981 | intron-variant | VAV1 | GRCh38.p7 | 19:6774350 | AGCCAGGATGGTCTC[A/C/G]ATCTCCCGACCTCAT | 7409 |
rs139984639 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6801795 | GCACACTGCTTCCCC[A/G]AAGGAGCGTGGAAAG | 7409 |
rs139987138 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | VAV1 | GRCh38.p7 | 19:6794121 | TTATTTACCAATAAA[C/T]CAACGGTAAATGATT | 7409 |
rs139988299 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6846415 | TACATGGTGAAACCC[C/T]GCCTCTATTAAAAGT | 7409 |
rs140010576 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6801220 | AATTAATGCATGACC[G/T]GGTCTGGGGTGCTGG | 7409 |
rs140109969 | snp | A/T | 0.00816982 | 0.063389 | intron-variant | VAV1 | GRCh38.p7 | 19:6853924 | CCCCAGACCCTTTTC[A/T]CACTTCTGTTCTCTC | 7409 |
rs140178188 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6784105 | CAAAAAATAAAAAAA[A/T]AAGCCCGGCATGGTG | 7409 |
rs140180309 | snp | G/T | 0.000856376 | 0.020675 | intron-variant | VAV1 | GRCh38.p7 | 19:6833885 | GGCATAGGTAGACAG[G/T]CTTTCTTTGTTTCTC | 7409 |
rs140191117 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805917 | AAGTGTCTTGGATGC[C/T]AAAGGGGTTTATGGG | 7409 |
rs140199574 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | VAV1 | GRCh38.p7 | 19:6831469 | GGTGCCCGCCACCAC[A/G]CCCAGCTAATTTTTT | 7409 |
rs140228514 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6835443 | AATTTTTTTGCTCAC[A/G]TTAGCCTTGAAGTTC | 7409 |
rs140267055 | snp | A/G | 1.64743e-05 | 0.00287 | missense | VAV1 | GRCh38.p7 | 19:6833921 | AGGACAAACTACATC[A/G]CAGGGCTCAGGACAA | 7409 |
rs140268248 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6824627 | ACCTCTGCCATCCAG[A/G]TTCAAGTGATTCTCC | 7409 |
rs140284735 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV1 | GRCh38.p7 | 19:6776839 | CTCGGCTCACTGCAA[C/T]GTCTGCTTCCTAGGT | 7409 |
rs140300013 | snp | A/G | 0.000104226 | 0.00721819 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822314 | CCTCATGCGCTCGGA[A/G]CCCGTGTCCATGCCG | 7409 |
rs140308261 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6815104 | CTAGAATTTAGTAAC[A/G]TTGTTTGAACCATAT | 7409 |
rs140313495 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6856911 | GGTCAGCCTTGTGTA[C/G]GTTGGGTGATGTGTT | 7409 |
rs140401873 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6812632 | CTCCAGCCTGGATGA[C/T]AGAGGGAGACTCTAT | 7409 |
rs140416583 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6840546 | CCTTGTGTTCCTCCC[A/G]CTTCGGCTTCCCAAA | 7409 |
rs140416947 | in-del | -/TA | 0.125182 | 0.216612 | intron-variant | VAV1 | GRCh38.p7 | 19:6805749 | GCTCACACATATGTG[-/TA]TATATATATGCACAC | 7409 |
rs140516956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792432 | GTGTCTAGGTTTACA[G/T]CTTAGGGACTTGCGT | 7409 |
rs140524743 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815766 | AGGATAATAATATGA[C/G]TTACCTTGAAGAGTT | 7409 |
rs140529761 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6840229 | CAGTATTTGTCCTTT[A/G]TGTCTAGCTTGTTTC | 7409 |
rs140562718 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6818315 | GGGTGTATTTGTTTG[C/T]GTGGGTGCCACAACA | 7409 |
rs140567307 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | VAV1 | GRCh38.p7 | 19:6846755 | ATTATATATTATAGG[G/T]TTATATATAACTATC | 7409 |
rs140632534 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843962 | AATTGCTGGCGCATC[A/C]GCTATTTAATGAGCT | 7409 |
rs140697515 | snp | A/G | 4.94597e-05 | 0.00497266 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772921 | GGCCCAGGCCCTCCG[A/G]GATGGTGTCCTTCTG | 7409 |
rs140730106 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6773420 | CAGAGTCTGGATGTG[A/G]GGGAGGAGCCTCCGC | 7409 |
rs140745065 | snp | C/T | 1.73372e-05 | 0.0029442 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848001 | GTCTCTTTGCAGGTA[C/T]GCAGGCCCCATGGAG | 7409 |
rs140755971 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6855018 | GCCTGCTTGAATTCC[A/G]ATTCCAAGGAGTGGA | 7409 |
rs140764965 | in-del | -/TATC | 0.498611 | 0.0263212 | intron-variant | VAV1 | GRCh38.p7 | 19:6838296 | TCGTCATCTACATAT[-/TATC]TATCTATCTATCTAT | 7409 |
rs140795872 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6808670 | TTCCTCCCTTTAAGA[A/C]TGCAACCTGGAATTG | 7409 |
rs140843047 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | VAV1 | GRCh38.p7 | 19:6826324 | GCCTGGGAGACAAGC[A/G]TGAAACCCCGTCTCA | 7409 |
rs140854128 | snp | C/T | 0.201727 | 0.245295 | intron-variant | VAV1 | GRCh38.p7 | 19:6832575 | TCCTTCCTCCCCTTC[C/T]TCCTCCTCGCCCTCC | 7409 |
rs140901031 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6814253 | AAAGCTAAATTCTTC[A/C]TTTTATCATTCAATC | 7409 |
rs141032943 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847244 | TTGCAATACTGCGCC[A/G]CCATCACTGCCGTTT | 7409 |
rs141064710 | snp | C/G/T | 9.95285e-05 | 0.00705381 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6822239 | CACGGTGGAGGAGGA[C/G/T]GAGGACCTGTATGAC | 7409 |
rs141228979 | in-del | -/AAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780113 | ATAATAATAATAATA[-/AAT]ATAATAATAATAATA | 7409 |
rs141236402 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6792013 | TGTGTGGAACTTAAG[C/G]GGGGGATGGGAAATC | 7409 |
rs141238479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843867 | ATAGCTCTTGCGATC[C/T]ACAGTGTCCATCTTC | 7409 |
rs141245046 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6819787 | TAGAATTCTTCAGGA[C/T]CTGGGGAACCTCAGA | 7409 |
rs141258805 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6784580 | CTCACGGCAGCCTCC[A/G]CCTCCCGGGTTCAAG | 7409 |
rs141269627 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6800682 | CAGGCTGTGCAGTGG[C/T]GTGATCTCGGCTCAC | 7409 |
rs141278487 | snp | C/T | 0.000153988 | 0.00877328 | missense | VAV1 | GRCh38.p7 | 19:6828106 | GCCAACAACGGGAGG[C/T]TCACCCTGCGGGACC | 7409 |
rs141320020 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6816315 | GTGAGCCACCATGCC[C/T]GGCTACAAAAACATT | 7409 |
rs141389450 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6809210 | TCCTGAGTAGCTGGA[A/T]CTATAGGCATGTGCC | 7409 |
rs141443224 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | VAV1 | GRCh38.p7 | 19:6783465 | GTGGCGCCATCACCT[A/C]CATCCTTTTTTTTTT | 7409 |
rs141451515 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | VAV1 | GRCh38.p7 | 19:6833446 | AAAGAGAACCCAAGG[A/G]GTCCCTTTATGTTTT | 7409 |
rs141454588 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855581 | CCCATTAAAACATTA[A/G]TCTATCCATTAATCC | 7409 |
rs141482421 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6807415 | TAGGGTTTGCACTCC[A/T]ATGAGGATCTAACGC | 7409 |
rs141555271 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6787012 | GCCCATTTGTTGACA[C/T]GCTGTCTATTTTTTT | 7409 |
rs141601475 | in-del | -/CTAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838222 | CATCTATTATCTATC[-/CTAT]TATATCATCATCATC | 7409 |
rs141670584 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6773907 | CATCTCCTCTGGGAT[A/G]AAAGGAGATACAGCC | 7409 |
rs141679910 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772110 | CGTATGTTCCTGGCA[C/T]GTTGGAGGAAGAGCG | 7409 |
rs141707090 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817645 | GGGGATAGAAAACGC[A/C/T]GGAGTAGGGGTGTGG | 7409 |
rs141730911 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | VAV1 | GRCh38.p7 | 19:6855407 | CCATCCATCTATCCA[C/T]CCATCCATCTATCCA | 7409 |
rs141747401 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | VAV1 | GRCh38.p7 | 19:6776914 | AGGCACCCGCCACCA[C/T]GCCCGGCTAATTTTA | 7409 |
rs141760749 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6802990 | TCAAGTCTTTGTAGC[A/G]GCTTTATTCATGATT | 7409 |
rs141763348 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771610 | AGCCAGACGCGGTGG[C/T]GGACGCCTGTAGTCC | 7409 |
rs141770459 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6799298 | TCAGCCTCTCGAACA[C/G]CTGGGACTACAGGTG | 7409 |
rs141817856 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6851059 | ATATATACATACATA[A/T]GTATGTATGTGTATT | 7409 |
rs141823895 | snp | C/T | 0.000692921 | 0.0186005 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821660 | GTCCTGGACCCCGAT[C/T]GCCCAGAACAGGGGG | 7409 |
rs141853006 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6796425 | TGAGACCACCCTTGG[C/T]TCACTCCCTTCCTCC | 7409 |
rs141872001 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | VAV1 | GRCh38.p7 | 19:6807517 | GAAGCTATGCTAGCT[C/T]ACCTGCCCACCACTC | 7409 |
rs141910165 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6848329 | AGAGGCTCAAAAAGG[C/T]TCTTAAAATTAATTA | 7409 |
rs141917636 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6838467 | ACTTATCAATACATT[A/C]ATGATCTATTCATCC | 7409 |
rs142022313 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770822 | GTTTGAGGCTGCAGT[C/G]AGCTATGATCATGCC | 7409 |
rs142096998 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6784388 | TTCAGCAAAATGGGT[C/T]GGGCTGATTGGAAAA | 7409 |
rs142118030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841275 | ATGTTTTGTTTATCC[A/G]TTTTCCTGTCAATGA | 7409 |
rs142154951 | in-del | -/ACCAATAAATCAACGGTAAATG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794107 | AACGGTAAATGATTT[-/ACCAATAAATCAACGGTAAATG]ATTTACCAATAAATC | 7409 |
rs142210698 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6838996 | CAACCTCCGCCTTCC[A/G]GTTTCAAGCGATTCT | 7409 |
rs142231623 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835911 | GAGTCTCACTCCATC[A/G]CCCAGGCTGGAGTGC | 7409 |
rs142309869 | snp | A/G | 0.000825968 | 0.0203052 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833220 | TGCCACCGCCAACGG[A/G]CATGACTTCCAGATG | 7409 |
rs142395562 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6778188 | GTGACCCACATGCCT[C/T]GGCCTCCCAAAGTGT | 7409 |
rs142402540 | snp | C/T | 0.00120734 | 0.02454 | intron-variant | VAV1 | GRCh38.p7 | 19:6850765 | GGCTTACGGTAAGGG[C/T]CAATGTCCGCTCAAT | 7409 |
rs142438533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804644 | CTGGTCTCAAATTTC[C/T]GACCTCAGGTGTTCT | 7409 |
rs142462175 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6796155 | CATTGGGGATTATAC[A/G]TTCCCAACATGTGCA | 7409 |
rs142499752 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6797397 | CTCTCATTCACTATG[A/T]TTTATCAAGAGTAGG | 7409 |
rs142537955 | snp | A/G | 8.23852e-05 | 0.00641762 | intron-variant | VAV1 | GRCh38.p7 | 19:6825027 | GGAATCTTATCTTCC[A/G]TCATCTTTCTCTCCC | 7409 |
rs142590220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821058 | GTTTCTCATCTGAAA[A/T]ATGGGAATATTATCA | 7409 |
rs142662847 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6814048 | CTGGGTGACAGAGTG[A/T]TACCCTGTCTCTAAA | 7409 |
rs142702635 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843627 | GGCCGGTTACTTAAC[C/T]TCCCTCTGTTTCAGC | 7409 |
rs142722522 | in-del | -/T | 0.0785177 | 0.181917 | intron-variant | VAV1 | GRCh38.p7 | 19:6823931 | GGTTTTTTTTGTTTC[-/T]TTTTTTTTTGATTTG | 7409 |
rs142733315 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | VAV1 | GRCh38.p7 | 19:6815244 | CCTCTACCTCCTGGC[C/T]TCAAGTGATCCTCCT | 7409 |
rs142773077 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV1 | GRCh38.p7 | 19:6798612 | GAGCCAGGATTGCAC[C/T]ACTGCACTCCAGTCT | 7409 |
rs142885675 | in-del | -/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800800 | AAATTTTTGTGTGTG[-/GT]TGTGTGTGTGCAGTC | 7409 |
rs142916472 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | VAV1 | GRCh38.p7 | 19:6801266 | CTACCGCAAACATTG[A/G]GTCAAGTATTTTCAT | 7409 |
rs142939702 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6777069 | CATCCATTCATCTAT[C/G]TATCATCCACCTGCC | 7409 |
rs142962365 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | VAV1 | GRCh38.p7 | 19:6831377 | AGTGCAGAGGCATGA[C/T]CTCGGCTCACTGCAA | 7409 |
rs142977186 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | VAV1 | GRCh38.p7 | 19:6783704 | AACTCCTGACCTCGG[A/G]TGATCCACTCGCCTC | 7409 |
rs142977252 | snp | C/T | 0.030665 | 0.119967 | intron-variant | VAV1 | GRCh38.p7 | 19:6814714 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 7409 |
rs142980433 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | VAV1 | GRCh38.p7 | 19:6803518 | AGTCAAGTTCCACCT[A/C]CTTCCTCGTATGGAT | 7409 |
rs142981034 | snp | C/T | 1.6782e-05 | 0.00289668 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821794 | CTGACCCCCCAGGCC[C/T]TTCCCCACCGAGGAG | 7409 |
rs142982570 | in-del | -/T | 0.103438 | 0.202533 | intron-variant | VAV1 | GRCh38.p7 | 19:6777808 | CAATTATGAATTTTG[-/T]TTTTTTTTAAATGAG | 7409 |
rs143017682 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811661 | CAGTCCTTTATTCAT[C/T]TCCCTGCATATAATT | 7409 |
rs143026875 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6824335 | CGGTCCATGGCAACC[A/T]CGAGCTTACTCGCTG | 7409 |
rs143029988 | in-del | -/AAGG | 0.46703 | 0.124089 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771793 | GAAAGGAAAGAAAGA[-/AAGG]AAGGAAGGAAGGAAG | 7409 |
rs143106907 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | VAV1 | GRCh38.p7 | 19:6852549 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7409 |
rs143128381 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | VAV1 | GRCh38.p7 | 19:6779571 | TAGTCTAAACCAGGG[A/G]GGGGCCTGGCTGGAT | 7409 |
rs143130996 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6828972 | CTCCTAGATGGGCAG[A/G]TGGGTGGAGTCAACA | 7409 |
rs143146240 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6805068 | GTAGAGTAAGGGGCA[A/G]TTTATGCAGAAATTT | 7409 |
rs143360936 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | VAV1 | GRCh38.p7 | 19:6814716 | TTTCTTTCTTTCTTT[C/T]TTTCTTTCTTTCTTT | 7409 |
rs143404448 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | VAV1 | GRCh38.p7 | 19:6844756 | TCAATGGGGTGGGGA[C/G]CAGGGTGAGACCAGG | 7409 |
rs143405380 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844519 | ACCTCGCCCAGCCGA[C/T]GCTCCCATCTTCTAA | 7409 |
rs143441037 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6799744 | TAACTCTTTGGAAGG[C/G]TGAGGCAGGAGGATT | 7409 |
rs143442846 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6854763 | GAATCACAGGGCAGC[A/G]TGGGAGCACTGAGGG | 7409 |
rs143487809 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849804 | GTCCATAGTGTGTGT[A/T]TATGTACCACATTTT | 7409 |
rs143545144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802974 | ACACAAAAACTTACA[C/T]TCAAGTCTTTGTAGC | 7409 |
rs143564425 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6833106 | GTGGTCTGTTCATAC[C/T]ATGGAATAGTATTCA | 7409 |
rs143570897 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6794291 | GTGGTCTGAGGGTTG[A/G]GCCTTAGGTTGTAAC | 7409 |
rs143617180 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV1 | GRCh38.p7 | 19:6843875 | TGCGATCCACAGTGT[C/T]CATCTTCTGCTGAAT | 7409 |
rs143676525 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV1 | GRCh38.p7 | 19:6838275 | ACCTATCATCTATCC[A/G]TCTATTCGTCATCTA | 7409 |
rs143693803 | snp | G/T | 0.039522 | 0.134904 | intron-variant | VAV1 | GRCh38.p7 | 19:6785833 | CCCAGCTAATTTTTG[G/T]ATTTTTAGTAGAGAT | 7409 |
rs143711229 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6794469 | ATGATTGCATCACTG[C/T]GCTCAGGCCTGGGCG | 7409 |
rs143779706 | snp | A/G | 0.0652144 | 0.168387 | intron-variant | VAV1 | GRCh38.p7 | 19:6789715 | TGATTCTCCTGCCTT[A/G]GCCTCCAGAGTGGCT | 7409 |
rs143825472 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797003 | AGCACTTTGGGAGGC[C/T]GAGACGGGTGGATCA | 7409 |
rs143826969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816731 | GCACTTTGGGAGGCC[A/G]AGGCAGGTGCATTAC | 7409 |
rs143848722 | snp | A/C | 0.00135226 | 0.0259674 | intron-variant | VAV1 | GRCh38.p7 | 19:6784168 | TTGAGGCAGGAGGAT[A/C]GCTTGAGCCCAGGAG | 7409 |
rs143849977 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6780686 | AAGAGATTCTCCTGC[C/T]TCAGCCTCCCGAGTA | 7409 |
rs143895678 | snp | C/G | 0.0260105 | 0.111035 | intron-variant | VAV1 | GRCh38.p7 | 19:6826280 | GAGATGGAGGTTGCA[C/G]TGAGCCCAGATCACA | 7409 |
rs143903552 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6812552 | GTAATCCCAGCTGTT[C/G]GAGAGGCTGAGGCAC | 7409 |
rs143953211 | snp | C/T | 0.0360663 | 0.129354 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771365 | CTGAGACAGGAGAAT[C/T]GCTTGAACCCAGGAG | 7409 |
rs143958994 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819565 | TTTTATGGCTGAGTA[A/C]TATTCCATTGTGTGG | 7409 |
rs143984583 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | VAV1 | GRCh38.p7 | 19:6831883 | GTGTGTGTGTGTGCA[C/T]GTGCACGCCTGCGTA | 7409 |
rs144148828 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | VAV1 | GRCh38.p7 | 19:6774229 | GCCTCCCAGGTTCAC[A/G]TCATTCTCCTGCCTC | 7409 |
rs144153515 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6819825 | GAACCTGTTGGGACG[G/T]TGGATGAGCCAATAC | 7409 |
rs144153581 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791531 | TGAGGTCCTTGAGCT[A/G]TGTCCTCATCTCAAG | 7409 |
rs144193852 | snp | C/T | 0.00112432 | 0.0236833 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826678 | CCTGGACCGTGTGGC[C/T]GCAGCCCGGGAGGAC | 7409 |
rs144210742 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6855534 | CCACCCTTCCACTCA[C/T]GCATCTATCTAACCA | 7409 |
rs144309768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812809 | GATTATAATGGTAAC[A/G]ATGATGGTGATGGTG | 7409 |
rs144384288 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777280 | CCATCCATCCATCCA[G/T]CCATCCAGCAATGAC | 7409 |
rs144402223 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808760 | AGACAATATTTGTTA[C/T]TCCAATTAATTTAGT | 7409 |
rs144402282 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6842767 | TGAACCTGGGAGATC[A/G]AGGCTGCAGTGAGCT | 7409 |
rs144416555 | snp | A/G | 0.0528381 | 0.153711 | intron-variant | VAV1 | GRCh38.p7 | 19:6808181 | GCCAGGTGTGGTGGC[A/G]GGTGCCTGTAATCCC | 7409 |
rs144462707 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6781839 | TCTCAAACTCCTGAC[C/G]TCGAGTGATCCACCC | 7409 |
rs144505599 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795490 | TATTTATTTATTTAT[G/T]TATTGAATTAATTTT | 7409 |
rs144506007 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6848708 | GTGCCTGGCCTGAAG[C/G]CTTTTATTTTTAACC | 7409 |
rs144541299 | in-del | -/TTTATTTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795468 | CCAGGGCGTAGTTCT[-/TTTATTTA]TTTATTTATTTATTT | 7409 |
rs144553245 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6778541 | GTTTCACCTCTCTGA[A/G]CTTCAGTTTCTCCAT | 7409 |
rs144555386 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6808040 | AAAAAAGGCCGGGCG[C/T]GGTGGCTCAAGCCTA | 7409 |
rs144593095 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV1 | GRCh38.p7 | 19:6776586 | TTCACCCACTCATCC[A/G]TCCATCCACTCATCC | 7409 |
rs144604064 | in-del | -/TTTG | 0.0573587 | 0.15934 | intron-variant | VAV1 | GRCh38.p7 | 19:6830434 | AAACAGAATTTTCAT[-/TTTG]TTTGTTTGTTTGTTG | 7409 |
rs144625519 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798115 | GACCCTGTCTGTACT[A/G]AAAATACAGAAATTA | 7409 |
rs144627727 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777282 | ATCCATCCATCCATC[A/C]ATCCAGCAATGACAA | 7409 |
rs144640161 | snp | A/C | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6773747 | TGTGGCTGTATGAGA[A/C]TGGCTCAGGAAATAT | 7409 |
rs144645256 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | VAV1 | GRCh38.p7 | 19:6802317 | GCACGTTGTGCACAT[A/G]TACCCTAAAATTTAA | 7409 |
rs144646579 | snp | C/T | 0.000395517 | 0.0140571 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772975 | ACCCCATGCCATCAA[C/T]CTGCGTGAGGTCAAC | 7409 |
rs144652980 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6825949 | TAATCCCAGTTACTC[A/G]GGAGAATTGCTTGAA | 7409 |
rs144682627 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6800481 | CACCCAGCTAATTTT[A/G]TATTTTTAGCAGAGA | 7409 |
rs144704046 | in-del | -/AC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816537 | CATACGCACACACAG[-/AC]ACACACACACACAGA | 7409 |
rs144736002 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823130 | TCTTTATCTATCTAT[C/T]TTTTTTTTTTTTGAG | 7409 |
rs144739934 | snp | A/G | 0.000181424 | 0.00952255 | missense | VAV1 | GRCh38.p7 | 19:6832115 | ATGTTCCTCCTGATC[A/G]AGGACCAAGGTGCCC | 7409 |
rs144765873 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6831158 | GGAGCTATCTTACCT[C/T]CATTGTTCAGGGACA | 7409 |
rs144766463 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV1 | GRCh38.p7 | 19:6798994 | TAGTTTGTATTTCCT[A/G]GAGTTTTATGTAAGT | 7409 |
rs144784152 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6781437 | AGCTGGATGGGAAAT[C/T]AGTGGAGCTCATTAA | 7409 |
rs144804488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827247 | GCCACATTCCAGTGG[A/G]TTTGTTTGTTTGTTT | 7409 |
rs144806213 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6796245 | GACTTGCTATTGAGT[C/G]TGTACTCGAGAGAGA | 7409 |
rs144849501 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776443 | CCATCCATCCATCCA[C/T]CCACCCACCCATCCA | 7409 |
rs144875056 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV1 | GRCh38.p7 | 19:6856212 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 7409 |
rs144896120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824100 | ATGCCACCACACCCT[A/G]CTTAATTCTTTAATT | 7409 |
rs144977995 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6806331 | ACCTTGTGATTCACC[C/T]GCCATGGGCTCCCAA | 7409 |
rs145028746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815417 | CAAAGTGCTGGGATT[A/G]CAGGTATGAGCCATC | 7409 |
rs145040547 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | VAV1 | GRCh38.p7 | 19:6792051 | CATTTAAGCAGATCA[A/G]TTGTTTAAAGAGGTC | 7409 |
rs145060742 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6789546 | ATGAGCCACCGCACC[C/T]GGCTCTTTCCTTTCT | 7409 |
rs145061892 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6841072 | TGTGAGCCACCATGC[C/T]GGGCCTAATTTTTGT | 7409 |
rs145085111 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838775 | CATTCTGTCACCTAG[A/G]CTGGAGTGCAATGGT | 7409 |
rs145133707 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | VAV1 | GRCh38.p7 | 19:6839877 | TTGTATTTTTCGTAG[C/T]GATGGGGTTTTGCCA | 7409 |
rs145180682 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6788536 | TAGGTGCCACCACAC[A/C]TGGCTAATTTTTGTA | 7409 |
rs145196954 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6840759 | ACAGGCATGTGCCAC[A/C]ATGCCTGGCTAATTT | 7409 |
rs145204838 | snp | A/G | 0.000307953 | 0.0124049 | missense | VAV1 | GRCh38.p7 | 19:6822318 | ATGCGCTCGGAGCCC[A/G]TGTCCATGCCGGTGC | 7409 |
rs145219365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785187 | CTCTCTGTCTTTTTT[C/T]GGAGAAGGGGGTCTT | 7409 |
rs145239714 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6850457 | CAACAAACCTGTGAG[C/T]CAGGGAAGATGATTC | 7409 |
rs145261631 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795973 | CAGGGGTGAGCCACC[A/G]CACCCGGCTAGTCCA | 7409 |
rs145265145 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | VAV1 | GRCh38.p7 | 19:6855178 | ATTTCTCAGAAATAT[A/G]TTTGTGTAATGAAGA | 7409 |
rs145344098 | in-del | -/G | 0.0633504 | 0.166319 | intron-variant | VAV1 | GRCh38.p7 | 19:6803178 | GTGAAAGTGCATAGC[-/G]GCAGTTGCAGAAGTC | 7409 |
rs145348573 | snp | C/T | 0.000153988 | 0.00877328 | missense | VAV1 | GRCh38.p7 | 19:6836435 | CCTGTCCTCCAGGTC[C/T]GCCCAAGATGGAGGT | 7409 |
rs145367293 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | VAV1 | GRCh38.p7 | 19:6824789 | CCCACCTCAGGCTCC[C/G]AAAGTGCTGGGATTG | 7409 |
rs145443661 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | VAV1 | GRCh38.p7 | 19:6827633 | AGATGGAGTCTCCCT[C/G]TGTCACCCAGGTTGG | 7409 |
rs145451984 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | VAV1 | GRCh38.p7 | 19:6823919 | TTTGTTTTGTTTTGG[G/T]TTTTTTTGTTTCTTT | 7409 |
rs145477808 | in-del | -/TC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785165 | CTTCAGGTTTCTCTT[-/TC]TCTCTCTCTCTGTCT | 7409 |
rs145489562 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | VAV1 | GRCh38.p7 | 19:6774370 | CCCGACCTCATGATC[C/T]GCCCACCTCGGCCTC | 7409 |
rs145498795 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6855435 | CCATCTATCTATCCA[C/G]AAATCATCCATTCAT | 7409 |
rs145542797 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6820607 | CTGTGCTTTCATTTC[C/T]CCTCCACACCAGTCC | 7409 |
rs145545128 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6782982 | GTCAGGAGTTTGAAA[C/G]CAGCCTGACCAATAT | 7409 |
rs145547215 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | VAV1 | GRCh38.p7 | 19:6832689 | CTCCTCTTCTTTCTC[C/T]TCCTCCTCCCTTTCC | 7409 |
rs145573343 | in-del | -/CTCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816491 | AGCATCTCTCTCTCG[-/CTCT]CTCTCTCTCTCTCTC | 7409 |
rs145581663 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6790763 | AGGCATATTTATCCC[A/G]TTTTAATTATATGCA | 7409 |
rs145590921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843273 | ATGCATTCTGTGATC[C/T]CTGAGCACCGACTTC | 7409 |
rs145675188 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6815993 | CCAGCCTCGGCAACA[G/T]AATGAAACTCTCTGT | 7409 |
rs145717503 | in-del | -/TAGGTGA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831125 | GAGATGTGGCTGTGG[-/TAGGTGA]GGGTGGGAGGGGGAG | 7409 |
rs145720593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848447 | ACAGAGTCCCTTTGT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs145730965 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6794311 | TAGGTTGTAACAGCA[C/T]AGAAACATTGGGGAG | 7409 |
rs145792893 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | VAV1 | GRCh38.p7 | 19:6843987 | TGAGCTCCTTTAATC[G/T]TCACAAAAGCCCTTC | 7409 |
rs145829522 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6841287 | TCCGTTTTCCTGTCA[A/G]TGAACAATTGGTTGC | 7409 |
rs145836391 | in-del | -/AAAAT | 0.393434 | 0.20476 | intron-variant | VAV1 | GRCh38.p7 | 19:6790179 | TGAGACTCTGTCTCA[-/AAAAT]AAAATAAAATAAAAT | 7409 |
rs146010502 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | VAV1 | GRCh38.p7 | 19:6795798 | AAGTGATTCTCCTGT[A/C]TCAGCCTCCCGAGCA | 7409 |
rs146018200 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | VAV1 | GRCh38.p7 | 19:6806441 | TTTGGAAGAGAAGCA[A/C]ACTCGTATGTGGGTT | 7409 |
rs146036757 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | VAV1 | GRCh38.p7 | 19:6822838 | TAAATAGAAAATATA[C/T]AAATATATACAAAGT | 7409 |
rs146048870 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV1 | GRCh38.p7 | 19:6820076 | GTAATCTCAGCACTT[C/T]AGGAGGCCAAGGTGG | 7409 |
rs146130884 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | VAV1 | GRCh38.p7 | 19:6783747 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 7409 |
rs146135758 | snp | C/G/T | 0.00123521 | 0.0248224 | intron-variant | VAV1 | GRCh38.p7 | 19:6833784 | AATAATGGGCAACAG[C/G/T]GCGGGGAGGACCCAG | 7409 |
rs146174304 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6803003 | GCGGCTTTATTCATG[A/T]TTGCTGAAACTGGGA | 7409 |
rs146230164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822118 | TGGAGTCTGAGGTCC[C/T]ACCCTTGGAGTCTTG | 7409 |
rs146242402 | snp | C/T | 0.030665 | 0.119967 | intron-variant | VAV1 | GRCh38.p7 | 19:6774109 | ATCCATGCGCCTTTA[C/T]TCCTTCTGTTTATTT | 7409 |
rs146253571 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771614 | AGACGCGGTGGCGGA[C/T]GCCTGTAGTCCCAGC | 7409 |
rs146255618 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6819814 | CAGAGAGTGCTGAAC[C/G]TGTTGGGACGTTGGA | 7409 |
rs146279380 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6852803 | TGGCTGCTCAGGGAG[A/G]TGATGAACTCCCCAT | 7409 |
rs146290324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850021 | CTCCAAACTGCTTTC[C/T]GCAGTGGCTGAACCA | 7409 |
rs146355078 | snp | C/T | 0.0157098 | 0.0872244 | intron-variant | VAV1 | GRCh38.p7 | 19:6833316 | GAGGGTCCTGCATAC[C/T]GGACTTGGTCATCAG | 7409 |
rs146389730 | in-del | -/AAAT | 0.339425 | 0.233459 | intron-variant | VAV1 | GRCh38.p7 | 19:6782330 | GTGAGACTCCATCTA[-/AAAT]AAATAAATAAATAAA | 7409 |
rs146390662 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787596 | TATTTATTTATTTAT[A/T]TATTTATTTATTTAT | 7409 |
rs146425089 | in-del | -/C | 0.0391387 | 0.134304 | intron-variant | VAV1 | GRCh38.p7 | 19:6784908 | CTACTCACAGCCCTT[-/C]CCCTGGTTCCCCACT | 7409 |
rs146438685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832264 | TGGGAAGGAGGAACG[C/T]GATCTAGTCCCTACT | 7409 |
rs146438720 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6800078 | TGAGGCGGGAGGATT[G/T]CTGGAGCCTAGGAGT | 7409 |
rs146449404 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6828560 | CTGATCCTCTAGCCG[A/G]GATTAGGTAGGAGCC | 7409 |
rs146452075 | in-del | -/CTT | 0.111576 | 0.20818 | intron-variant | VAV1 | GRCh38.p7 | 19:6775938 | TTTCTCTTCGGAGTC[-/CTT]CTCTTTTTTCTCAGT | 7409 |
rs146513546 | in-del | -/TTTG | 0.0256215 | 0.110247 | intron-variant | VAV1 | GRCh38.p7 | 19:6827588 | TCTTCCCATTGCTTT[-/TTTG]TTTGTTTGTTTGTTT | 7409 |
rs146535757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791796 | CATGCTTTCTGGAGG[C/G]TGGTCAAGGAAAGCT | 7409 |
rs146561902 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | VAV1 | GRCh38.p7 | 19:6817976 | CAGGCATGAGCCACC[A/G]CGCCCAGCCTTAAAT | 7409 |
rs146606591 | in-del | -/TTTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787614 | TTATTTATTTATTTA[-/TTTA]AAGTCTAAGTTTTGC | 7409 |
rs146639456 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | VAV1 | GRCh38.p7 | 19:6781972 | CTTTGTGGTCTTGGA[G/T]AAAAAAATAATTACT | 7409 |
rs146653352 | snp | C/T | 0.100231 | 0.200173 | intron-variant | VAV1 | GRCh38.p7 | 19:6778937 | GCTGGAGTGCAGTGG[C/T]ATGATCACAGCTCAC | 7409 |
rs146676980 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6805354 | CGCTTGAACCCGGGA[A/G]GTGGAGGTTGCAGCG | 7409 |
rs146688193 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802905 | CTATGTGTCAGACAT[A/G]GTACTAGGTATTGAG | 7409 |
rs146698172 | in-del | -/ATCTATCT | 0.472616 | 0.113763 | intron-variant | VAV1 | GRCh38.p7 | 19:6855803 | TCCATCCACCCATTC[-/ATCTATCT]ATCTATCTATCTATC | 7409 |
rs146773724 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815673 | TGGCATAATGGTTAC[C/G]CACAGGCTTGGAAGT | 7409 |
rs146801322 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6846527 | CAGGAGGCAGAGGTT[G/T]CAGTGAGCCAAGACA | 7409 |
rs146810540 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843916 | GGAAGTGTTCTTTCA[C/T]AATGGCACATAAAAG | 7409 |
rs146852359 | snp | A/G | 0.000197674 | 0.00993972 | missense | VAV1 | GRCh38.p7 | 19:6833918 | TCCAGGACAAACTAC[A/G]TCGCAGGGCTCAGGA | 7409 |
rs146884598 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6804868 | AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC | 7409 |
rs146896195 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794849 | CATAGTGATGATGGT[A/G]CCTCAGCTCCATGGT | 7409 |
rs146906652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6793061 | TATATATGGCCGGGC[A/G]CGGTGGCTCACACCT | 7409 |
rs146906896 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6821176 | GGAGGCTGAGGTGGG[C/T]AGATCACGAGGTCAG | 7409 |
rs146929911 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6819293 | GGAACATATGAATAT[C/G]CAGTCCTAAAAACTA | 7409 |
rs146975138 | snp | C/G | 0.00590936 | 0.0540348 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6850751 | AAAGGCTTTCCGGGG[C/G]CTTACGGTAAGGGTC | 7409 |
rs147012630 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810264 | GAAGATTGCTTGAGC[C/T]CAATTTCAAGGCTGC | 7409 |
rs147035649 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | VAV1 | GRCh38.p7 | 19:6807417 | GGGTTTGCACTCCTA[C/T]GAGGATCTAACGCTG | 7409 |
rs147082518 | in-del | -/TTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780551 | CATTAAAAGATTGCC[-/TTTT]TTCTCCTTTTCTTTC | 7409 |
rs147118762 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6851136 | GGTACATGTATATAC[A/G]TGTATCTGTTTATTT | 7409 |
rs147150931 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6845001 | ATTCAAAATGTTGAT[A/G]TTTGTTCATCATGGT | 7409 |
rs147160914 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6842185 | CTGTGAGCCAAGATC[A/G]CGCCATTGCACTCCA | 7409 |
rs147170322 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6790403 | CACGGATCGGATGTC[G/T]TAGAACAAAGGACAT | 7409 |
rs147170363 | in-del | -/GAAAG | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771786 | GAGAAAGAAAGGAAA[-/GAAAG]GAAAGAAAGGAAGGA | 7409 |
rs147254003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830736 | TGAGCCACTGTGCCC[A/G]GCTTATTTTATTTCT | 7409 |
rs147265428 | snp | C/G/T | 0.0103417 | 0.0712888 | intron-variant | VAV1 | GRCh38.p7 | 19:6773362 | CCCCAGAACCCCCAG[C/G/T]GTGGCCATTGGGTTA | 7409 |
rs147266875 | snp | C/T | 1.64798e-05 | 0.00287047 | missense | VAV1 | GRCh38.p7 | 19:6828134 | ACCTGCTGATGGTGC[C/T]TATGCAGCGAGTTCT | 7409 |
rs147277528 | snp | C/G | 0.0248432 | 0.108648 | intron-variant | VAV1 | GRCh38.p7 | 19:6826287 | AGGTTGCACTGAGCC[C/G]AGATCACACCACTGT | 7409 |
rs147278126 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | VAV1 | GRCh38.p7 | 19:6777891 | CTGCAGCCTCCACCT[C/T]CCAGGTTCAAGCAAT | 7409 |
rs147284652 | in-del | -/TATT | 0.304688 | 0.243945 | intron-variant | VAV1 | GRCh38.p7 | 19:6804413 | TGGCGGTCCTATTTA[-/TATT]TATTTATTTATTTAT | 7409 |
rs147310822 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | VAV1 | GRCh38.p7 | 19:6855954 | TATCTACTGTGTGCC[A/G]GGAACTGTTCTAGGC | 7409 |
rs147361076 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | VAV1 | GRCh38.p7 | 19:6817383 | AATGCAAATATTGTT[A/G]TGGTAGGGGCACAGA | 7409 |
rs147384636 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815273 | CTGCCTCAGCCTCCC[A/T]AGTAGCTGGGACTAC | 7409 |
rs147447114 | snp | A/C | 6.59739e-05 | 0.00574305 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6832156 | GCTGTTCTTCAAGAC[A/C]AGAGAATTGAAGAAG | 7409 |
rs147454364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6777203 | TCTACCCATCCATCC[A/G]TTCATTCATCCATCC | 7409 |
rs147463984 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | VAV1 | GRCh38.p7 | 19:6774329 | AGACAGGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 7409 |
rs147480002 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856730 | CTCTGTCTCAAAAAA[A/G]AAAAAAAAAAAAAAA | 7409 |
rs147489942 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6801124 | ATTACATAAGCCCTG[G/T]AAGGGCAGAGCTCTG | 7409 |
rs147546726 | in-del | -/TTTA | 0.239431 | 0.266964 | intron-variant | VAV1 | GRCh38.p7 | 19:6838892 | GCCATTATGCTCAGC[-/TTTA]TTTATTTATTTATTT | 7409 |
rs147606199 | snp | C/G/T | 0.0107391 | 0.0726353 | intron-variant | VAV1 | GRCh38.p7 | 19:6839987 | CTGAGCCGCCATGCC[C/G/T]GGCCAACATAACCAT | 7409 |
rs147625642 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6785284 | TCAAGTGATCCTCTC[A/G]CCTCTGCCTCCCAAA | 7409 |
rs147626890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835637 | AATCATACAGTACAT[A/G]CTTATTTCATCTGGT | 7409 |
rs147649416 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849106 | ATTTTTTTTTTCAAC[A/T]TATTTTAGAATCAGA | 7409 |
rs147688028 | in-del | -/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831854 | CTTCTGCAAAGGGGA[-/GT]GTGTGTGTGTGTGTG | 7409 |
rs147708649 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6775990 | GGAAAGAACATATTC[A/T]TCCATCCGTTCATCC | 7409 |
rs147731100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773098 | CTGACGTGCTGCTCC[A/G]CCTCTGGGCCTGCAA | 7409 |
rs147731320 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6820641 | AGCTAGGTGGCCTGG[A/G]GGTCAGTTTCTCCCC | 7409 |
rs147740863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854584 | AAAACATTAGTTGGG[C/T]GTGGTAGTGTGTCCC | 7409 |
rs147764536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851229 | GCCCAGGCTGGAGTG[C/T]AGTGGTGCAATCATA | 7409 |
rs147803914 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | VAV1 | GRCh38.p7 | 19:6784579 | GCTCACGGCAGCCTC[C/T]GCCTCCCGGGTTCAA | 7409 |
rs147836946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808903 | GGATACCTTTAGCTA[A/G]GTGCTTGTCTCTGCT | 7409 |
rs147883329 | snp | C/T | 8.23649e-05 | 0.00641683 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6820797 | AGCCTTTGACCTCTT[C/T]GATGTGCAGGATTTT | 7409 |
rs147921520 | snp | A/G | 0.00108452 | 0.0232613 | intron-variant | VAV1 | GRCh38.p7 | 19:6853901 | CCCAGAGAGTGAGTG[A/G]GTATCTGCCCCAGAC | 7409 |
rs147940209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796403 | ACGGTTTGGGCATAT[C/T]GGCACCTGAGACCAC | 7409 |
rs147970425 | in-del | -/AAGA | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771755 | CAAAAAAAAAAAAAG[-/AAGA]AAGAAAGAAACAAAG | 7409 |
rs148027176 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV1 | GRCh38.p7 | 19:6795707 | TTTGTTTTTTGAGAT[A/G]GAGTCTCACTCTGTC | 7409 |
rs148037335 | snp | C/T | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857511 | CCACAGACAAAGCCC[C/T]CTCAACAATCCACAG | 7409 |
rs148087819 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | VAV1 | GRCh38.p7 | 19:6807429 | CTATGAGGATCTAAC[A/G]CTGCAGCTGATCTGA | 7409 |
rs148123070 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831126 | AGATGTGGCTGTGGT[A/G]GGTGAGGGTGGGAGG | 7409 |
rs148162938 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6789758 | ATGTGCCACCATATC[C/T]GGCTAATTTTTGTAT | 7409 |
rs148164388 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6841560 | GCTCACTGCAACCTC[C/G]GCTTCCCAGGTTCAA | 7409 |
rs148238627 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6819684 | TGCTTTAGGACTCTT[A/G]GTCCAGACTGACTTC | 7409 |
rs148244465 | snp | A/G | 0.000164791 | 0.00907569 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828090 | GGAATGTTCTCAGAG[A/G]GCCAACAACGGGAGG | 7409 |
rs148255206 | in-del | -/AT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782720 | CCCCATCTCTACAAA[-/AT]ATATATATATATTAG | 7409 |
rs148310984 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV1 | GRCh38.p7 | 19:6783357 | TAGGGCCGAGGCTCC[A/G]TCATCTCATGGTCTT | 7409 |
rs148336249 | in-del | -/C | 0.238749 | 0.249747 | intron-variant | VAV1 | GRCh38.p7 | 19:6838228 | ATTATCTATCTATAT[-/C]ATCATCATCATCATC | 7409 |
rs148374674 | in-del | -/TATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838215 | ATCTACCCATCTATT[-/TATC]ATCTATCTATATCAT | 7409 |
rs148374760 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6814745 | TTCCTTTTTCCCTCT[A/G]TCTTGTCTTGCAGTA | 7409 |
rs148428113 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6839698 | AAAGTTAACAATGTA[A/C]CCTTTTTTTTGGAGA | 7409 |
rs148470055 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6843448 | GGTGGTGATGGTAAT[A/G]ACAGTTCCAGTTGTT | 7409 |
rs148478621 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6790888 | GTGTTGCCATGGCAA[C/T]GGTAAACTGACATAG | 7409 |
rs148500301 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6798448 | GCCTGGGCAACATGG[A/T]GAGACCAGCCTCATC | 7409 |
rs148510385 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | VAV1 | GRCh38.p7 | 19:6826063 | TAAAAACAGGCCAGG[C/T]GTGGTGGCTCACGCC | 7409 |
rs148614647 | snp | C/G | 0.00149813 | 0.027328 | intron-variant | VAV1 | GRCh38.p7 | 19:6784223 | TGTGCTACCACTGTA[C/G]TCCAGACTGGACAAA | 7409 |
rs148633264 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | VAV1 | GRCh38.p7 | 19:6793290 | AGTGAGCCGAGATCG[C/T]GCCACTGCACTCCAG | 7409 |
rs148698236 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | VAV1 | GRCh38.p7 | 19:6823388 | CCTCGGCCTCCAAAA[G/T]TGCTGGGATTGCAGG | 7409 |
rs148710574 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | VAV1 | GRCh38.p7 | 19:6774274 | CTGGGACTACAGGCG[C/T]CCGCCACCACGCCTG | 7409 |
rs148722167 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | VAV1 | GRCh38.p7 | 19:6855546 | TCACGCATCTATCTA[A/T]CCATCTATCCACCTA | 7409 |
rs148773063 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6804562 | GCTGGGATTACAGGC[A/G]CGTGCCACCACGCCT | 7409 |
rs148778427 | in-del | -/TTA | 0.182614 | 0.240747 | intron-variant | VAV1 | GRCh38.p7 | 19:6788351 | ATGATTCTTTTTATT[-/TTA]TTATTATTATTATTA | 7409 |
rs148834111 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855809 | CACCCATTCATCTAT[C/T]TATCTATCTATCTAT | 7409 |
rs148859143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802955 | GAGTTGAACATTTAT[A/G]TCCACACAAAAACTT | 7409 |
rs148869408 | in-del | -/TACG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816524 | ACGCACACAGACACA[-/TACG]CACACACAGACACAC | 7409 |
rs148882420 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6832986 | CCCCTGGAAACTCCT[A/C]GCCTGCTTTCTCTTT | 7409 |
rs148923431 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6837136 | TGGAAAGACACCCCC[A/G]GAGTTGGGGAGGGGG | 7409 |
rs148954420 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6794366 | AAAACCAGGCCAGGC[A/G]TGGTGGCCCATGCCT | 7409 |
rs148964450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6820594 | CATGGAAGAGGGTCT[A/G]TGCTTTCATTTCCCC | 7409 |
rs149015516 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6824321 | CTCTTATCTTCCCCC[A/G]GTCCATGGCAACCAC | 7409 |
rs149038511 | snp | A/C/T | 0.0158469 | 0.0875917 | intron-variant | VAV1 | GRCh38.p7 | 19:6856411 | AGACGGTGATATGTG[A/C/T]TATAGAAAAAGATAA | 7409 |
rs149065980 | snp | C/T | 0.0755793 | 0.179102 | intron-variant | VAV1 | GRCh38.p7 | 19:6779001 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 7409 |
rs149087852 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | VAV1 | GRCh38.p7 | 19:6789291 | AGAGTCTCACTCTGT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs149092107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806417 | AAAATAATTTTTTCT[C/T]AATGCCGTTTTGGAA | 7409 |
rs149144422 | snp | A/G | 0.207559 | 0.246371 | intron-variant | VAV1 | GRCh38.p7 | 19:6810637 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 7409 |
rs149207101 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | VAV1 | GRCh38.p7 | 19:6844248 | ATGATGATGCTCCCA[A/T]CTTCTTGTTGCCCAG | 7409 |
rs149228521 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6854658 | AGTTGGATGCTGCAG[A/T]GAGCTATGATTGTGC | 7409 |
rs149240889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839667 | TTTTTGATTATGGCA[A/C]AATATATAGAACATA | 7409 |
rs149261251 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795369 | CTGAACTCTGTGTAT[C/G]GCTCGCGAAATAGGA | 7409 |
rs149330066 | snp | A/G/T | 0.00019778 | 0.00994249 | missense | VAV1 | GRCh38.p7 | 19:6850701 | AAGCACATTAAAATC[A/G/T]TGACAGCAGAAGGAC | 7409 |
rs149336151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6825853 | AATATGGTGAAACCC[C/T]GTCTCCATCGCCTAA | 7409 |
rs149410289 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | VAV1 | GRCh38.p7 | 19:6789714 | GTGATTCTCCTGCCT[C/T]GGCCTCCAGAGTGGC | 7409 |
rs149420051 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6816702 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7409 |
rs149472666 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6819488 | TTTGTGATTTGCTTC[C/T]TTCACTGAGCATGTT | 7409 |
rs149495492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852450 | TTTTTGGCCGGGCAC[A/G]GTGGCTCACGCCTGT | 7409 |
rs149526373 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6774219 | TGCAAGCTCCGCCTC[C/T]CAGGTTCACGTCATT | 7409 |
rs149537483 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6855515 | CATCTATCCATTCAT[C/T]CACCCACCCTTCCAC | 7409 |
rs149610699 | snp | A/G/T | 0.000148747 | 0.00862272 | intron-variant | VAV1 | GRCh38.p7 | 19:6833630 | ACATGGGCAAGGTAC[A/G/T]AGTGGGAGGGAGGCT | 7409 |
rs149628170 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6793057 | ACCATATATATGGCC[A/G]GGCGCGGTGGCTCAC | 7409 |
rs149661002 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6787892 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT | 7409 |
rs149712876 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790555 | ATGATCCAGGACAGG[A/C/T]GAGCCCCTAGATTGG | 7409 |
rs149735573 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817812 | CTCTCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 7409 |
rs149788030 | in-del | -/CTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814610 | CTTCTGCAAAAATGA[-/CTTT]CTTTCTTTCTTTCTT | 7409 |
rs149791166 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV1 | GRCh38.p7 | 19:6820320 | AGCTCACCGCAGGCT[C/T]GAACTCCTGGGCTCA | 7409 |
rs149801768 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | VAV1 | GRCh38.p7 | 19:6853766 | TTTTCTAAATTCAGA[C/T]GGGAGGATGATGCTG | 7409 |
rs149854150 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6856164 | TAGCTGGGCATTGTG[A/G]CGTGCGCCTCTAATC | 7409 |
rs149865022 | snp | C/T | 0.0696598 | 0.17314 | intron-variant | VAV1 | GRCh38.p7 | 19:6784153 | CAGCTACTCAGGAAG[C/T]TGAGGCAGGAGGATC | 7409 |
rs149926701 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6815384 | TGACCTCAAAGTGAT[C/T]CTCTCGCCTTGGTTT | 7409 |
rs149928017 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6835470 | GTTCTCAATAATGGC[C/T]TGTGGCTAGTTGCTA | 7409 |
rs149949691 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6846314 | ATTATGGGCTGGGCA[C/T]GGTGGCTTATGCCTG | 7409 |
rs149991130 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850319 | TATTTCCACCATGTT[A/G]ACAGAAATGGGTCTT | 7409 |
rs150000296 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | VAV1 | GRCh38.p7 | 19:6795929 | ACCTCGTGATCCGCC[C/T]GTCTCAGCCTCCCAA | 7409 |
rs150055151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6799373 | CAGGGTTTCACCATG[C/T]TGACCAGGCTGGTCT | 7409 |
rs150058721 | snp | A/G | 1.65493e-05 | 0.00287652 | missense | VAV1 | GRCh38.p7 | 19:6833212 | CCGGAGAATGCCACC[A/G]CCAACGGGCATGACT | 7409 |
rs150084540 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6795320 | CAATCAGGTTAATGA[C/G]CTACATGAACCTTGA | 7409 |
rs150094750 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821669 | CCCGATCGCCCAGAA[C/T]AGGGGGATCATGTGA | 7409 |
rs150109367 | snp | C/T | 0.00202607 | 0.0317636 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822281 | TGAGGAGGCGGAAGG[C/T]GACGAGATCTATGAG | 7409 |
rs150115567 | snp | A/G/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6782955 | GGGAGGCCAAGGCAG[A/G/T]TGGATCATGAGGTCA | 7409 |
rs150149959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825706 | GGCCTGGCACATAGT[A/G]GATGCTCAATAAGTA | 7409 |
rs150162861 | snp | A/G | 5.19314e-05 | 0.00509539 | missense | VAV1 | GRCh38.p7 | 19:6848002 | TCTCTTTGCAGGTAC[A/G]CAGGCCCCATGGAGC | 7409 |
rs150167531 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | VAV1 | GRCh38.p7 | 19:6785578 | TTCAGGTGATCTGCC[C/T]GCCTCAGCCTTTCAA | 7409 |
rs150173217 | snp | G/T | 0.00159617 | 0.0282053 | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857678 | AAATTCCCTCTTTTG[G/T]GCTGGGCATGGTGGC | 7409 |
rs150245135 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6816561 | CACACAGAACGTGGG[C/T]TCTAGATTCATACCA | 7409 |
rs150254257 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | VAV1 | GRCh38.p7 | 19:6847300 | CAAGAGAAACCCCAT[A/C]CCGGGCAGTTGCTCC | 7409 |
rs150305144 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797288 | TCTGAATGATCAAAG[C/G]CCTCTCACCTGCTAC | 7409 |
rs150305653 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | VAV1 | GRCh38.p7 | 19:6851285 | TTTAAATAATCTCTC[A/G]CCTCAGCCTCCCGAG | 7409 |
rs150380298 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV1 | GRCh38.p7 | 19:6830022 | ACATCTACATGGAAG[C/T]GTGTGTTAATCCACT | 7409 |
rs150402582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840714 | AGCTTAAGTGATCCT[C/T]CCACTTCAGCCTCCT | 7409 |
rs150453557 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6792751 | TGTGGGGCAGCAGTG[A/G]GGGCGAGGGGAGTGA | 7409 |
rs150497834 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6814817 | TAGCAGGTTCCGTTG[C/T]GTAGTTCTGATTTCA | 7409 |
rs150519501 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787595 | TTATTTATTTATTTA[A/T]TTATTTATTTATTTA | 7409 |
rs150572457 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6849564 | GTGATCCACCTGCCT[C/T]GGCCTCTCAAAGTGC | 7409 |
rs150645363 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | VAV1 | GRCh38.p7 | 19:6807663 | GCTGCAGTGAGCTGT[A/C]ATCATGCCACTGCAC | 7409 |
rs150696392 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | VAV1 | GRCh38.p7 | 19:6812026 | TTAAATACAGTGCCC[C/T]GAAAGTGATGCTTAT | 7409 |
rs150696527 | in-del | -/ATG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812831 | GTGATGGTGGTGATA[-/ATG]ATGATGATGATGATG | 7409 |
rs150706231 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | VAV1 | GRCh38.p7 | 19:6841952 | CACTTTCGGCCGGGC[A/G]CGGTGGTTCACGCCT | 7409 |
rs150760063 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6793453 | GTAAAGGGTGATTTG[C/T]TGGGGGAGCTTATGG | 7409 |
rs150761537 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6845962 | ACATTTATGTTTATA[C/T]ATCATATGCGTTATA | 7409 |
rs150812060 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6795838 | ACAGGCGCGTGCCAC[C/T]GCGCCCAGCTAATTT | 7409 |
rs150845501 | in-del | -/TCACCAA | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857538 | ACAGACAAAGCCCCC[-/TCACCAA]TCACAGACAAAGCCC | 7409 |
rs150853254 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6783627 | AGCTGGGATTACAGG[A/C]ATGCACCATCACACC | 7409 |
rs150857750 | snp | C/T | 1.77106e-05 | 0.00297573 | intron-variant | VAV1 | GRCh38.p7 | 19:6833513 | GCTCTTCTTTATGTG[C/T]TCCCTGCATCTCAGA | 7409 |
rs150909389 | snp | C/T | 0.039522 | 0.134904 | intron-variant | VAV1 | GRCh38.p7 | 19:6787858 | GAGGCAGGTGGATCA[C/T]GAGGTCAGGAGATCG | 7409 |
rs150932007 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV1 | GRCh38.p7 | 19:6854852 | ATAAGGGATAAATAA[A/G]GTCATGCAAATGAAA | 7409 |
rs150942717 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6782437 | TTAAACATGATAAGG[G/T]AAATGAAATTCCCAG | 7409 |
rs150952336 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | VAV1 | GRCh38.p7 | 19:6808570 | CTGTTCTGTTCTTCC[A/G]CCACCTGTGAATTTC | 7409 |
rs151026997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843696 | TCATAGTGTTTTTAG[C/G]AGGCGTAAATGAGTC | 7409 |
rs151078917 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6794617 | CAACAAAAGCAATAG[A/G]TCACTTTAATGAGCA | 7409 |
rs151082686 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | VAV1 | GRCh38.p7 | 19:6847156 | TGACCTTGTGATTCG[C/T]CCACCTCGGCCTCCC | 7409 |
rs151088451 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822227 | AACCCACAGCGACAC[A/G]GTGGAGGAGGATGAG | 7409 |
rs151100897 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6801564 | CTCTCTGGGAACCCT[C/G]GGGAGCTTGAGGTTG | 7409 |
rs151102330 | in-del | -/CCATCCAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776160 | TGCTCATCTATCCAC[-/CCATCCAT]CCATCCATCCATCCA | 7409 |
rs151144571 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6824592 | GCTGGAGTGCAGTGG[C/T]GTGATCTCAGCTCAC | 7409 |
rs151163671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835190 | TTGTACAATAGAATA[C/T]ATATATGTGTATATA | 7409 |
rs151183567 | in-del | -/TTATTATTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788351 | ATGATTCTTTTTATT[-/TTATTATTA]TTATTATTATTATTA | 7409 |
rs151222361 | in-del | -/TCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832653 | CTTTCCTCCCCTTCT[-/TCC]TCCTCCTCCTCCTCC | 7409 |
rs151227171 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | VAV1 | GRCh38.p7 | 19:6789434 | ATTTTTTATATTTTC[A/G]TAGAGATGGGGTTTC | 7409 |
rs151241479 | in-del | -/TCTA/TCTATCTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838097 | CTGTCTGTCTGTCTG[-/TCTA/TCTATCTA]TCTATCTATCTATCT | 7409 |
rs151268869 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6792312 | CATTTTCATTGAGGA[A/G]GAAGGGTGGAGGTGG | 7409 |
rs151291596 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818085 | TCCACCTCCCAACGT[C/G]CTGGGATTACAGGTG | 7409 |
rs151310298 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827394 | CAACTCCTACCTTGG[C/G]CTCCTGAGTAGCTGG | 7409 |
rs180941653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774650 | ATGTTGGCCAGGCTA[A/G]TCTTGAACTCCTGAC | 7409 |
rs180973924 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792587 | TGTTTTGTTTTGTTT[C/G]TTTTTGTAGAGACAG | 7409 |
rs180994398 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | VAV1 | GRCh38.p7 | 19:6821270 | GCTGGGTGTGGTGGC[C/T]GGCGCCTGTAGTCCC | 7409 |
rs181002081 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814727 | CTTTCTTTCTTTCTT[G/T]CTTTCCTTTTTCCCT | 7409 |
rs181014713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832385 | AATGCAGGGGTTGTG[C/T]GCAAGCTTCAGTTAC | 7409 |
rs181019900 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804912 | GTATTTTTAGTAGAG[A/C]TGAGTTTTCACCATG | 7409 |
rs181023259 | snp | C/T | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857489 | CAGACAAAGCCCCCT[C/T]AACAATCCACAGACA | 7409 |
rs181030404 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6849982 | GCATCAAATGGTGGT[C/T]CTATTTTTAGTTCTT | 7409 |
rs181031222 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6840372 | GAGCAGTGGCGCAAT[C/G]TTGGCTCACTGCAAG | 7409 |
rs181080487 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6836180 | TGCCCAGCCAGGACA[A/C]ATGTTTTCATTTCTC | 7409 |
rs181092991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6853617 | AGGCCTGTAATCCCC[A/G]TGATTCAGGAGGCTG | 7409 |
rs181162973 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV1 | GRCh38.p7 | 19:6779887 | GAGGCCGAGGCGGGC[A/G]GATCACAAGGTCAGG | 7409 |
rs181275318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800872 | CCTCAAGTGATCCGC[C/T]CGCCTCAGCCTCCCA | 7409 |
rs181279029 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817711 | TTATTTTCTGAGATG[A/G]GGTCTCGCTCTGTTG | 7409 |
rs181286851 | snp | C/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770955 | TCAGGAGTTTGAGAC[C/G]AGCCTGGCCAACATG | 7409 |
rs181292833 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | VAV1 | GRCh38.p7 | 19:6774349 | TAGCCAGGATGGTCT[C/T]GATCTCCCGACCTCA | 7409 |
rs181310438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784765 | TCCCAAAGTGCTGGG[A/T]TTACAGACGTGAGCC | 7409 |
rs181312403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6820876 | TTTCTATTGACGTCT[A/G]CACTGGGCAAGCTAA | 7409 |
rs181314940 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | VAV1 | GRCh38.p7 | 19:6804769 | TGCTCTGTCGCACAG[C/G]CTGGAGTGCAGTGGC | 7409 |
rs181319682 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6798216 | TGGGAGGCGGAGGTT[G/T]CAGTGAGCGGAGATC | 7409 |
rs181332257 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814683 | CTTCCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 7409 |
rs181341839 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6831896 | CATGTGCACGCCTGC[A/G]TATGTGGTTTTGGGT | 7409 |
rs181395320 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791950 | AGGGAGAGTGGTAAA[C/G]AATGAGGTTTGGGAG | 7409 |
rs181473123 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | VAV1 | GRCh38.p7 | 19:6849257 | ACCCTCCTCCCTCTA[A/G]TGCTCCCCCGAGTCT | 7409 |
rs181517119 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6786736 | TGCAGTGAACCACGA[C/T]TGCACCACTGCACTC | 7409 |
rs181659104 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6844002 | TTCACAAAAGCCCTT[C/T]GGAAAATAGATTTGA | 7409 |
rs181687120 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800726 | TCCTGGGTTCAAGCG[A/C]TTCTCCTGCCTCAGC | 7409 |
rs181688912 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6817219 | TGCCTGGCTAATTTT[G/T]TTTGTTTGTTTTTTT | 7409 |
rs181724687 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6805544 | CCCAGGGGTTCGAGA[A/C]CAGCCTGGGCAACAT | 7409 |
rs181730532 | snp | C/G | 0.000722804 | 0.0189968 | intron-variant | VAV1 | GRCh38.p7 | 19:6821908 | TGGAGCACCGTCCTG[C/G]GGGTGGAGGGTGTGG | 7409 |
rs181732403 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840792 | CTACTTTTAAAAAAA[A/T]TTTTGAGATGGAGTT | 7409 |
rs181740021 | snp | A/C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857788 | AACATGGCAAAACCC[A/C/T]GTCTCTACTAAAAAT | 7409 |
rs181848525 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6795265 | AAATGTAGTTGTCTT[C/T]CTGGCAGCGCAAAAC | 7409 |
rs181857782 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6775671 | TGCCCTTTGAAGCCC[A/G]GCCGTGTGTCTGGTA | 7409 |
rs181858478 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | VAV1 | GRCh38.p7 | 19:6853234 | TGTCTATCCCTTCCT[A/T]TATATATTTTAATAT | 7409 |
rs181859577 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | VAV1 | GRCh38.p7 | 19:6826104 | GCACTTTGGGAGGCC[A/G]AGGAGGGCAGATCAC | 7409 |
rs181871279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793014 | AGCTGTGGGATCTTG[A/G]GCAAGTTATCAAATG | 7409 |
rs181899065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780042 | CATGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 7409 |
rs181909734 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6795097 | CAGAAGCTGCAAGGC[A/G]TCTTCTAACCTACTT | 7409 |
rs181912317 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6808244 | TTGAACCCAGGAGGC[A/G]GAGTTTGCAGTGAGC | 7409 |
rs181915349 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6825916 | AAACAATTAGCTGGG[C/T]GTGGTGGCATGCACC | 7409 |
rs181919341 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6848982 | TATTTTTTGTAGAGA[C/T]GAGGGTCTCTCCTTG | 7409 |
rs181941218 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6843409 | GATGACGATGATGAC[A/G]ATGATGATGATGATA | 7409 |
rs182074220 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6783082 | CTACTCAGGAGGCTG[A/T]GGCAGGAGAATGGCT | 7409 |
rs182086991 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6813583 | GTCTTAATATTTGGT[A/G]GGACTCATACCCTTT | 7409 |
rs182109018 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835537 | TCAGAAAGCACTGCT[A/C]CTCACCTATCTCCCA | 7409 |
rs182117882 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809512 | TTAGCGTGTGGCAAC[A/C]ACTTCCACCTGGCTG | 7409 |
rs182178831 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771523 | ACTTTGGGAGGCTGA[A/G]GCGGGCGGATCATGA | 7409 |
rs182180147 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827683 | AGCTCAATGCCATCT[C/T]TGCCTCCCGGGTTCA | 7409 |
rs182184457 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801783 | GCCTCTGTCCCTGCA[C/G]ACTGCTTCCCCGAAG | 7409 |
rs182188587 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6845317 | TTGAACCTGGCAGGC[A/G]GAGGTTGCAGTGAGC | 7409 |
rs182377123 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6798006 | ACATTGGTGGGGCGC[A/G]GTGGCTCACGCTGTA | 7409 |
rs182384361 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776289 | ATCTATCCACTCATC[C/T]ATCCATCCATCCATC | 7409 |
rs182389592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818629 | GGCAGTATTTGGATA[C/T]GGAGTATTTACAGAG | 7409 |
rs182391130 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831498 | TTTGTATTTTTAGTA[A/G]AGACGGAGTTTCACC | 7409 |
rs182399306 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6838168 | TCTATATATCATCTA[C/T]CTATTTACCTATCAT | 7409 |
rs182406565 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6855079 | TTTCTGCCAAGTTCT[A/C/G]ATTTTTGTTCCATGA | 7409 |
rs182416895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798756 | ACTCAAGCGATCCTC[C/T]TACCCTAGCCTCCTG | 7409 |
rs182429609 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6778233 | TTAAGCCACCACGCC[C/T]AGACACCACTGTGCT | 7409 |
rs182442153 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6793699 | CTAGGGACAGCAAAT[A/G]ATGTAGAACTCAGGA | 7409 |
rs182470470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818015 | GTAGAAATGGGATCT[C/T]ATTATGTGGCCCCAG | 7409 |
rs182496428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795728 | TCACTCTGTCGCCCA[A/G]GCTGGAGTGCAGTGG | 7409 |
rs182598059 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6786278 | TAACACAGGGGCTGG[C/T]AAATGATAACTCATG | 7409 |
rs182616281 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6799527 | TTACATAGGTATACA[C/T]GTGCCATGGTGGTTT | 7409 |
rs182616452 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6840916 | TCGAGTAGCTGGGAT[C/T]ACAGGCATGCACCAC | 7409 |
rs182669874 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780643 | ATGACGTGATCTCAG[C/T]TCACTGGAACCTCCA | 7409 |
rs182733254 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6823218 | ACAATCTCTGCCTAC[C/T]GGGCTCAAGCAATCC | 7409 |
rs182766201 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6855684 | GTTAATCTATCTCTA[C/T]ATTTATCCATCCATA | 7409 |
rs182780946 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6809934 | CCAGCACTTTGGGAA[A/G]CCAAGACAAGCTAAT | 7409 |
rs182788725 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789941 | CCAGACGTGGTGGCT[C/T]ATGCCTGTAATCTCA | 7409 |
rs182797100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816494 | CATCTCTCTCTCGCT[C/T]TCTCTCTCTCTCACA | 7409 |
rs182801391 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6844858 | ATGCAACATTAAAAA[A/G]AATCAAAAACAAGCC | 7409 |
rs182813215 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833083 | ATGAATGAGTGGACA[C/T]GCAAAACGTGGTCTG | 7409 |
rs182984432 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6785524 | TTTAGTAGAGACGGA[C/G]TTTCACCATGTTGGC | 7409 |
rs183000730 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772033 | ATGTAGGGGTGAGGG[A/T]GCTAGCCATGAAGTT | 7409 |
rs183007881 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6806808 | AAGAGAAAGAGGAAA[G/T]GGTATGGATGTGTGC | 7409 |
rs183011353 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802685 | TTATGCCACTCTCTA[A/C]GAGGCACCAGGAGCA | 7409 |
rs183022199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6841190 | AAAGTGCTAGGATTA[C/T]AGGCATGAGCCACCG | 7409 |
rs183026363 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6818312 | TCAGGGTGTATTTGT[C/T]TGCGTGGGTGCCACA | 7409 |
rs183028091 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837586 | CACTTCACAGCCTGC[A/C]GAGGGAAATTCTCTC | 7409 |
rs183038319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854631 | GAGGTGGGAGGATTG[C/T]TTGAGTCCAGGAGTT | 7409 |
rs183059527 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6776781 | TGTTTATTTATTTAC[A/G]GCGTCTCACTCTGTC | 7409 |
rs183065900 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772291 | TGGGCAGAAGAAGGG[C/T]GTGCCCTGACTCAGA | 7409 |
rs183079315 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6805640 | CACACATGAGTTGGG[C/G]GGATGGTTTCAGGAT | 7409 |
rs183086833 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826810 | GGTCCACTTTCTGCT[A/G]CAGCCCAGCCAGAGA | 7409 |
rs183098944 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803020 | TGCTGAAACTGGGAG[C/G]CAACAAATTGTCCTT | 7409 |
rs183250071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807448 | CAGCTGATCTGACAG[A/G]AGGTGGGGCTCAGGT | 7409 |
rs183253148 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6824121 | TTCTTTAATTTTTTT[G/T]GTAGATATGGGGTCT | 7409 |
rs183360274 | snp | C/T | 0.00111156 | 0.0235488 | intron-variant | VAV1 | GRCh38.p7 | 19:6822200 | AGAGGTCCAAGGGAT[C/T]CCTGACCTCACAACC | 7409 |
rs183450103 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6781304 | ATTGCCAAATTGTTA[C/T]CCGTCTGGGATTGTT | 7409 |
rs183466303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6796014 | AAGCCTAGATATCCT[C/T]TCTTGTGACCGTCTC | 7409 |
rs183470941 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810462 | TAATCCCAGCACTTT[A/G]AGAGGCAGAGGTGGG | 7409 |
rs183564225 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | VAV1 | GRCh38.p7 | 19:6797701 | AGAGTGAAAGATCGC[A/G]CCATTGCACTCCAGC | 7409 |
rs183576711 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812780 | AATACTATTGTGGTA[A/G]TGATGGTGGTGATGA | 7409 |
rs183578199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6831267 | TGAACTCTTCCGTTC[A/G]CTTCAGTTTTTGCCC | 7409 |
rs183583124 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848323 | TCCTATAGAGGCTCA[A/G]AAAGGCTCTTAAAAT | 7409 |
rs183585863 | snp | C/T | 0.000298894 | 0.0122212 | intron-variant | VAV1 | GRCh38.p7 | 19:6850775 | AAGGGTCAATGTCCG[C/T]TCAATCCCAGCTTTC | 7409 |
rs183607081 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6796311 | TATTTGTCCTTCTTT[A/G]TAGGGACCCCGGGAG | 7409 |
rs183620965 | snp | C/T | 4.94434e-05 | 0.00497184 | intron-variant | VAV1 | GRCh38.p7 | 19:6828769 | AGAGTGTGTGTCTGG[C/T]TCCTTTCTTGGGAGA | 7409 |
rs183622756 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851221 | GCTCTGTTGCCCAGG[A/C]TGGAGTGCAGTGGTG | 7409 |
rs183792849 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6816742 | GGCCGAGGCAGGTGC[A/G]TTACTTGAGATCAGT | 7409 |
rs183796044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6794483 | GCGCTCAGGCCTGGG[C/T]GACACAATGAGATTC | 7409 |
rs183799569 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6808089 | AGGCCGAGGCAGGTG[A/G]ATTGCCTGAGGTCAG | 7409 |
rs183819770 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6781390 | CGCCTCCCCGACAGA[A/C]GGTTCTGTTGCCAAG | 7409 |
rs183824924 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6782286 | AGTGAGCCAAGATTG[C/T]ACCACTGCACTCCAG | 7409 |
rs183831291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6811117 | CTCAGCTCACTGCAG[C/T]CTCCGCCTTCCAGGT | 7409 |
rs183835491 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6797077 | TCTCCACTAAAAATA[C/G]AAAAATTAGCCAGGC | 7409 |
rs183848606 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846576 | AAAAAAATTATATAT[G/T]ATATATAATTATGTA | 7409 |
rs183851470 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6811642 | GAACTTTTAGCCCAG[A/T]CAGCAGTCCTTTATT | 7409 |
rs183856408 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | VAV1 | GRCh38.p7 | 19:6830548 | AGGTTCAAGCAATTC[C/T]CCTGCCTCAGCCTCC | 7409 |
rs183869885 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6799113 | TACCATTCTGTTGTA[C/T]GGATGCACCCCAGTT | 7409 |
rs183888717 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832653 | CCTTTCCTCCCCTTC[C/T]TCCTCCTCCTCCTCC | 7409 |
rs184057930 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6856812 | CTTGCAATTTTGAAT[A/G]GTATGGCTAGGAAGG | 7409 |
rs184228473 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6803949 | GGAACCCCAAATGCA[C/T]ATTACTAAGTGAAAG | 7409 |
rs184235761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6782780 | CCGGCTACCTAGGAC[A/G]CTGAGGCAGGAGGAT | 7409 |
rs184243249 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | VAV1 | GRCh38.p7 | 19:6838469 | TTATCAATACATTCA[C/T]GATCTATTCATCCAC | 7409 |
rs184362178 | snp | A/T | 1.65353e-05 | 0.00287531 | missense | VAV1 | GRCh38.p7 | 19:6825102 | CTCAAGACATTGAGA[A/T]CATCTTTATCAACAT | 7409 |
rs184375182 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6819276 | CCTATTGAGCCTTTA[C/T]AGGAACATATGAATA | 7409 |
rs184468501 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787379 | TGGGGTTTCACCAAG[C/T]TGGCAAGGCTGGTCT | 7409 |
rs184468649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800734 | TCAAGCGATTCTCCT[C/G]CCTCAGCCTCCAGAG | 7409 |
rs184474368 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817302 | CTCCTGACCTCAAGT[A/T]ATCTGCCTGCCTCTG | 7409 |
rs184487445 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835933 | CTGGAGTGCAGTGGC[A/G]TGATCTCAGCTCACT | 7409 |
rs184494650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843026 | CACATAATAGGCACT[C/G]ACTAAATGCAAGTGG | 7409 |
rs184517367 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853245 | TCCTATATATATTTT[A/T]ATATAATATAATTTA | 7409 |
rs184530691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799599 | GAATGCTATCCCTCT[C/T]CTAACCCCCAGCCCC | 7409 |
rs184538127 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6839514 | CTCAAATGATCTGCC[C/T]GCCTCGGCCTCCCAA | 7409 |
rs184546903 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856254 | GTGAGCTGAGATCGC[A/G]CCACTGCACTCCAGC | 7409 |
rs184599075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792015 | TGTGGAACTTAAGGG[A/G]GGGATGGGAAATCCT | 7409 |
rs184618886 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6847398 | TTTCCTATGAATGGA[A/G]ATCACACAGTGTGTG | 7409 |
rs184628709 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6820906 | AGGACTGTCAGGGGA[C/T]AGGCAGACAAGCCAG | 7409 |
rs184655580 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6786417 | CAGTGAACTATGATC[C/T]TGCCACTGCACTCCA | 7409 |
rs184693516 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6774161 | GAGACGGAGTCTCAC[G/T]CTGTCACGCAGGCTG | 7409 |
rs184708959 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804526 | GGTTCAAGCAATTCT[C/T]CTGCCTCACCCTTCT | 7409 |
rs184711056 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6791733 | ACATTGTAATAAATG[A/T]CACAGATGAAACAAA | 7409 |
rs184720680 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820472 | CCACATTTGTTTAAC[C/T]GTTAGTGATTAATTT | 7409 |
rs184721581 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | VAV1 | GRCh38.p7 | 19:6774475 | GGGTCTCACTCTGTC[G/T]CCCAGGCTGGAGGCA | 7409 |
rs184737403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779028 | ACTACAGGTGTGCAC[C/T]GGCATACCTGGGTGA | 7409 |
rs184747320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804792 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 7409 |
rs184754719 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV1 | GRCh38.p7 | 19:6794035 | TTACCAATAAACCAA[C/T]GGTAAATGATTTATT | 7409 |
rs184779159 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6840017 | TTTTCTAAGGTACAG[C/T]TGAGTGGCATTAAGT | 7409 |
rs185005274 | snp | C/T | 0.000216384 | 0.0103993 | intron-variant | VAV1 | GRCh38.p7 | 19:6773063 | GACGGGGGTCCTCCC[C/T]GGGGCTGACAGTCGA | 7409 |
rs185018549 | snp | A/G/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6774881 | TGTCCCAGCCTCCCA[A/G/T]GTAGCTGCGACTACA | 7409 |
rs185026376 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | VAV1 | GRCh38.p7 | 19:6792831 | ATCACTACTGGAGGG[C/T]TTGGTGTGTTATTGA | 7409 |
rs185026747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6805167 | CAGCGGTTCATGCCT[A/G]TAATCCCAGCACTTT | 7409 |
rs185080588 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | VAV1 | GRCh38.p7 | 19:6779845 | GGCCGGGCACGGTGA[C/T]TCACACCTGTAATTC | 7409 |
rs185106128 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6841964 | GGCGCGGTGGTTCAC[C/G]CCTGTAATCCCAACA | 7409 |
rs185190374 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831724 | TCTGGGGACCACATC[C/G]TATTCACTGCTCTGT | 7409 |
rs185191779 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6794303 | TTGGGCCTTAGGTTG[C/T]AACAGCATAGAAACA | 7409 |
rs185210862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824559 | TTTTTTGAGATAGAG[C/T]CTCACTCTGTCACCC | 7409 |
rs185292723 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6832466 | CTTCCTTCTCCTCCT[C/T]CTGGTTTCCTTCCTC | 7409 |
rs185300962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849996 | TTCTATTTTTAGTTC[C/T]TCGAGAAACCTCCAA | 7409 |
rs185327441 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6780844 | CTCCCAAAGTGCTGG[A/G]ATTACACGTGATAGC | 7409 |
rs185339708 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6795934 | GTGATCCGCCCGTCT[C/T]AGCCTCCCAAAGTGC | 7409 |
rs185345918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836378 | GTGGGTGGCAAGATT[C/T]AGGGTTGAAAGTTGA | 7409 |
rs185354485 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6810071 | TGTAGTCCCAACACT[C/T]AGGAGGTTGAGGCAA | 7409 |
rs185354646 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6853643 | GGCTGAGGCAGGAGA[A/C]TCACTTGAACCCAGG | 7409 |
rs185356866 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6827048 | CTCACTGAACCCCAA[C/T]TCCAACCAACCCCTG | 7409 |
rs185405527 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6786478 | AAAATAAATTAATTT[A/T]AAAAATTAAAAATGA | 7409 |
rs185423597 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6817087 | GAATCTCACTCTTGT[G/T]GCCCAGGCTGGAGTG | 7409 |
rs185437711 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6852732 | TCTCAAAGAAAAAAA[A/G]AAAAGAAAGAAAGAA | 7409 |
rs185539571 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6800413 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTTCCTCTG | 7409 |
rs185562227 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835167 | AAATTAGAAACAACC[C/T]GTGTCCTTTGTACAA | 7409 |
rs185575000 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785168 | CAGGTTTCTCTTTCT[C/G]TCTCTCTCTGTCTTT | 7409 |
rs185592745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798262 | AGCCTGGGCAACAGA[A/G]TGAGACTCTGTCTCA | 7409 |
rs185595209 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814687 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 7409 |
rs185603510 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6832306 | TGCCATGGGACCACT[C/G]TGAACCACAGTCTCT | 7409 |
rs185806488 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849349 | GCTGGAGTGCAATGG[C/G]ATGATCTCAGCTCAC | 7409 |
rs185868541 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6775931 | TCTGTCATTTCTCTT[C/T]GGAGTCCTTCTCTTT | 7409 |
rs185891230 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793056 | GACCATATATATGGC[C/T]GGGCGCGGTGGCTCA | 7409 |
rs185899439 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822010 | GTCTGGGGAGACACA[G/T]CCCTGCCCTGGGGTC | 7409 |
rs185911211 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | VAV1 | GRCh38.p7 | 19:6840849 | GAATGGTGCAATCTC[G/T]GCCCACTGCAACCTC | 7409 |
rs185916100 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6785549 | GTTGGCCAGGCTGGT[C/T]TCAAACTCCTGACTT | 7409 |
rs185918730 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6840375 | CAGTGGCGCAATCTT[G/T]GCTCACTGCAAGCTC | 7409 |
rs185929264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6814946 | TACTTTGCCAAGAGA[C/T]TTTTTTCCCCCTCTT | 7409 |
rs185970568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800917 | CAGGCGTGAGCCACC[A/G]CACCCAGCCGCTCAC | 7409 |
rs186037429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6821362 | GCCGAGATGGTGCCA[C/T]TGCACTCCAGCCTGG | 7409 |
rs186042017 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6798851 | GTGCAACTATGAACC[C/T]AGCCTTGAAATCAAT | 7409 |
rs186056008 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857526 | CCTCAACAATCCACA[A/G]ACAAAGCCCCCTCAC | 7409 |
rs186096847 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6788279 | GTTCGATGGAAAATA[A/G]GGGGGTTGGCTTTCT | 7409 |
rs186103837 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | VAV1 | GRCh38.p7 | 19:6817937 | GTGATCCGCCCGCCT[C/T]GGCCTCCCAAAGTGC | 7409 |
rs186133366 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6795146 | CTTACAGCAGTTTTC[C/G]TAACAAGAAGCCATA | 7409 |
rs186136430 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6808569 | CCTGTTCTGTTCTTC[C/T]GCCACCTGTGAATTT | 7409 |
rs186140577 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771530 | GAGGCTGAGGCGGGC[A/G]GATCATGAGATCGGG | 7409 |
rs186143536 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6844981 | GGCAGTCAGATTCTG[C/T]CTTTATTCAAAATGT | 7409 |
rs186146160 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771445 | CGAGAGTGAAACTCC[A/G]TCTCAAAAGAAAAAA | 7409 |
rs186148864 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6825917 | AACAATTAGCTGGGC[A/G]TGGTGGCATGCACCT | 7409 |
rs186152991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843616 | GTATGACCTTGGGCC[A/G]GTTACTTAACCTCCC | 7409 |
rs186482240 | snp | A/T | 0.0433465 | 0.140692 | intron-variant | VAV1 | GRCh38.p7 | 19:6851352 | TAATTTTAAAAAAAA[A/T]TTTTTTTTTTGTAGA | 7409 |
rs186483354 | snp | C/T | 4.5042e-05 | 0.00474542 | missense | VAV1 | GRCh38.p7 | 19:6822274 | TGGAGAATGAGGAGG[C/T]GGAAGGCGACGAGAT | 7409 |
rs186675756 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6806118 | TTGAGATGGAGTCTC[A/G]CTCTGTCACCCAGCC | 7409 |
rs186695760 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6780532 | GCACTGAATACTTAC[C/T]ATTGCATTAAAAGAT | 7409 |
rs186696387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6840997 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTGA | 7409 |
rs186713521 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809584 | GTCATCAGAGAAGTC[A/C]GCAGGGGCCGTGGTG | 7409 |
rs186724628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855458 | CCATTCATCTGTGCA[C/T]CCATCCATCTTAGCC | 7409 |
rs186733357 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6844665 | GAGGTCTTAGAACAC[A/G]TAAGAGGCAGGGTCA | 7409 |
rs186735526 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | VAV1 | GRCh38.p7 | 19:6847714 | CCTGGTGAAGCCATC[A/G]CCAAATTCCAGACAC | 7409 |
rs186759139 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798015 | GGGCGCGGTGGCTCA[A/C]GCTGTAATCCCAGCA | 7409 |
rs186759327 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778283 | GCTGCGGAGATGGAA[A/C]TTGAAGGCCAAGAGA | 7409 |
rs186780103 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6793723 | CTCAGGAGACATTCC[C/T]GGGAGTGGGGTTAAT | 7409 |
rs186792823 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6823222 | TCTCTGCCTACCGGG[C/T]TCAAGCAATCCTTCT | 7409 |
rs186924721 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795515 | AATTTTATTTATAAC[A/T]CTAATGGGTAAGCAG | 7409 |
rs186932995 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6826455 | TGCTACAATAGCCTC[A/G]CATGGGAGATGCTAT | 7409 |
rs186977619 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813713 | TTTTTAATTGAAATT[A/G]GATTAAATCTATAGC | 7409 |
rs187053410 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784528 | AGACAGAGTTTCACT[A/C]TCTCTCCCAGGCTGG | 7409 |
rs187118052 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786290 | TGGCAAATGATAACT[C/G]ATGGGCCCAAGCTGC | 7409 |
rs187136548 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6799528 | TACATAGGTATACAC[A/G]TGCCATGGTGGTTTG | 7409 |
rs187139903 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816496 | TCTCTCTCTCGCTCT[C/T]TCTCTCTCTCACACG | 7409 |
rs187154627 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6851055 | ATGCATATATACATA[C/T]ATATGTATGTATGTG | 7409 |
rs187160972 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6783207 | ACAAAAACAAACAAA[A/G]CCAAACCCTCAAAAC | 7409 |
rs187203279 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854670 | CAGTGAGCTATGATT[A/G]TGCCACTGCAGCCTG | 7409 |
rs187269960 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6802047 | ATAATGCCTCTCCTA[A/C]GTTTGTTTAAAGGAC | 7409 |
rs187314297 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6818081 | CACTTCCACCTCCCA[A/G]CGTGCTGGGATTACA | 7409 |
rs187324266 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772117 | TCCTGGCATGTTGGA[A/G]GAAGAGCGAAGAGGC | 7409 |
rs187329649 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6854312 | GACATTGTGCTGGGT[A/G]TCGAGGAGACAGAAA | 7409 |
rs187344031 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6802689 | GCCACTCTCTAAGAG[A/G]CACCAGGAGCAGCTT | 7409 |
rs187345340 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6789851 | TGACCTGCCTGCCTT[A/G]GCCTCCCAAAGTGCT | 7409 |
rs187355764 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6818452 | CTCCAGCCACATGGG[C/T]CTCCTTGCTGTTCCT | 7409 |
rs187360348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837751 | TCTCTCTACCCACAC[A/G]TAGTATTTATTTTTC | 7409 |
rs187433459 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6841527 | GTCCCCAGGCTGGAG[A/T]GCAATGGAATGATCT | 7409 |
rs187437418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816764 | GAGATCAGTTCAAGA[C/G]CAGCCTGGACAACAT | 7409 |
rs187574956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807451 | CTGATCTGACAGGAG[G/T]TGGGGCTCAGGTGGT | 7409 |
rs187579669 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6824336 | GGTCCATGGCAACCA[C/T]GAGCTTACTCGCTGT | 7409 |
rs187582264 | snp | A/G | 0.000165511 | 0.00909549 | intron-variant | VAV1 | GRCh38.p7 | 19:6837097 | CAAGGGGTCCAGGGC[A/G]GGTCCTGGGAGGATG | 7409 |
rs187589036 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6841886 | TTTGTTTGTTGATTT[C/G]TTTTTGCCTTATAGT | 7409 |
rs187618943 | snp | C/T | 0.0178098 | 0.0926698 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772635 | GTGCTCCCCCAGCTC[C/T]CCCCCGCCCCATGGC | 7409 |
rs187639334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803241 | CTGTGAGCCCGGAGT[A/G]ATCAGGGTTGCAGTC | 7409 |
rs187655045 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838376 | ATCAATCCATCCATT[C/T]ATCAATCAGTTCTTC | 7409 |
rs187685888 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6799690 | TGGCTATCATGAATC[A/G]AGTTGCTAGCTGGAT | 7409 |
rs187874433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793572 | AATGTGCAGGACCCA[A/G]TGCTTATATAGTACA | 7409 |
rs187905842 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790395 | CAAAGAACCACGGAT[C/T]GGATGTCTTAGAACA | 7409 |
rs187931820 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818975 | ACAAAAATAAGCTGG[A/G]TGTGATGGCGGGTGC | 7409 |
rs187955806 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | VAV1 | GRCh38.p7 | 19:6780035 | AGAATGGCATGAACC[C/T]GGGAGGCGGAGCTTG | 7409 |
rs187967687 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6795055 | GAAACCCGGAGAGAG[A/C]GCAAGTATTCCTCAA | 7409 |
rs187981785 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808105 | ATTGCCTGAGGTCAG[A/G]AGTTTGAGACCAGCC | 7409 |
rs187981947 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6825685 | TGACTATACGGATGC[A/G]CACAGGGCCTGGCAC | 7409 |
rs187994426 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6843234 | CCAGGCTGGGTATGG[C/G]AGGAACCTCCGAGCC | 7409 |
rs188006638 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6810485 | GAGGTGGGTGGATCC[C/T]CTGAGGTCAGGAGTT | 7409 |
rs188022427 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6827831 | TCTTGAACTCCTGAC[C/G]TCAAGTGATCCTCCC | 7409 |
rs188022639 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6791019 | TCCTGCCTCCTATTT[C/G/T]ACATGCATCCTTGGA | 7409 |
rs188026455 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6846262 | TATAATATACATTAC[A/T]TTAACAAGAGATATT | 7409 |
rs188026677 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804269 | GCCTCACAGGCTAAG[C/G]AAAGAATTCAAGGGT | 7409 |
rs188161586 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | VAV1 | GRCh38.p7 | 19:6776826 | GCAGGGGCATGATCT[C/T]GGCTCACTGCAACGT | 7409 |
rs188191886 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6846810 | ATAGATAGTTATATA[C/T]TATTATATAATGATT | 7409 |
rs188208966 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | VAV1 | GRCh38.p7 | 19:6782618 | GCACAATGGCTCACG[C/G]CTATAATCCCAACAC | 7409 |
rs188226625 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6797163 | CTTGAACTCAAGAGG[C/T]GGAGATTGCTGTGAG | 7409 |
rs188228712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811965 | CCCTTAGAGTCTCAG[C/T]CTGCAGAAAATAGGG | 7409 |
rs188238535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830858 | TTTGGGAGGCCGAGG[A/T]GGGAGAATTGCTTGA | 7409 |
rs188374159 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6811186 | GATTACAGGCATGCA[C/G]CACCATGCCCGGCTA | 7409 |
rs188416416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6799118 | TTCTGTTGTACGGAT[A/G]CACCCCAGTTTGTTT | 7409 |
rs188419915 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779547 | TTTTGCTCGCCCTGT[A/G]CTAGACATTAGTCTA | 7409 |
rs188437823 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832662 | CCCTTCTTCCTCCTC[C/T]TCCTCCTCTTCCTCC | 7409 |
rs188471347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830012 | TTGCCAGACTACATC[G/T]ACATGGAAGTGTGTG | 7409 |
rs188652089 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6796728 | TTAAAATTGCACCCC[C/G]TCCTGACATTCTCCA | 7409 |
rs188686575 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6786163 | TGTCTATTTTACGTC[C/T]CCCAGTGCTTTAGAA | 7409 |
rs188710254 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6794125 | TTACCAATAAATCAA[C/T]GGTAAATGATTTATT | 7409 |
rs188712393 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6815832 | GAAAATTGAGAGCAT[A/G]GTGGGTGGAAGCTCA | 7409 |
rs188727618 | snp | C/T | 0.000116812 | 0.00764148 | intron-variant | VAV1 | GRCh38.p7 | 19:6850650 | CCCAGACTCAGGGCC[C/T]GGTGACCATCTGGTT | 7409 |
rs188832643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787816 | ACATGGTGGCTCACA[C/T]CTGTAATCCCAGCAC | 7409 |
rs188846694 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817562 | CAGAACGATGGCCCT[A/C]CCCTCTTCAAACTGA | 7409 |
rs188853122 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6836122 | CAGGTGATCTTCCTG[C/G]CTCGGCCTCCCAAAG | 7409 |
rs188862446 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6853401 | CCTCAGCCTCAAAAT[A/C]AAAAAATAAAAATAA | 7409 |
rs188883736 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796111 | GTGATCTAATCACCT[C/T]TTAAAGGTCCCGCTT | 7409 |
rs188884397 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6791919 | AAGGAGCTTCTGGAA[C/G]GAAGGGAGTGAGTGG | 7409 |
rs188889223 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6783892 | GGACGCAAAGAAGTC[A/C]CTGCCGTAGAACCTC | 7409 |
rs188891525 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804564 | TGGGATTACAGGCGC[A/G]TGCCACCACGCCTGA | 7409 |
rs188907512 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6839559 | AGGCGTGAGCCACCA[C/T]GCCCGGCTGGGTATG | 7409 |
rs188913561 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6856301 | GACTGTGTCTCAAAA[A/G]AAAAAAAAATTCTGC | 7409 |
rs188914861 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6819626 | AGATGCATGCAATAC[A/G]TGGCTTTGGAAGATG | 7409 |
rs188936172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855886 | TCCACCTACCCATCA[A/G]TCCAATAATCCATCC | 7409 |
rs189138137 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786531 | CTCACGCCTGTAATC[G/T]TAAGACATTGGGAGG | 7409 |
rs189158402 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6800500 | TTTTAGCAGAGACAG[G/T]TTTCACTATATGTTG | 7409 |
rs189161350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6781307 | GCCAAATTGTTATCC[A/G]TCTGGGATTGTTTCC | 7409 |
rs189173321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786455 | CAACACAGCAAGCCC[A/G]TCCCTGTAAAATAAA | 7409 |
rs189210046 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | VAV1 | GRCh38.p7 | 19:6838949 | CTCTTGTTTCCCAGG[C/G]TGGAGTGCAGTGGGG | 7409 |
rs189244996 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6826082 | GTGGCTCACGCCTGT[A/C]ATTCCAGCACTTTGG | 7409 |
rs189252910 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843974 | ATCAGCTATTTAATG[A/T]GCTCCTTTAATCTTC | 7409 |
rs189256961 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6774523 | CACTGCAACCTTAGC[C/T]TCTCAGGATCAAGCA | 7409 |
rs189261120 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804874 | GACTACAGGCGCCCG[C/G/T]CACCATGCCCGGCTA | 7409 |
rs189481278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840369 | GGAGAGCAGTGGCGC[A/G]ATCTTGGCTCACTGC | 7409 |
rs189488185 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6831310 | TGTGCTCTGGTCTGT[A/G]GCTTCTCTATTTCTT | 7409 |
rs189498236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6848672 | CCTCCCAAAGTGTTG[A/G]GATTACAGGCGTGAG | 7409 |
rs189506511 | snp | C/T | 1.67829e-05 | 0.00289675 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821803 | CAGGCCCTTCCCCAC[C/T]GAGGAGGAGAGTGTA | 7409 |
rs189534738 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792474 | TCTTCTACTGTAGTA[A/G]GAAGACTAGGGGAGG | 7409 |
rs189691366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780903 | TATACCATATTTTAT[A/G]CAAAGATTTCTTATC | 7409 |
rs189713374 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6795984 | CACCGCACCCGGCTA[C/G]TCCACTCTGAGATCA | 7409 |
rs189717785 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6810338 | CTGTCTCTAAAGAAA[G/T]AAAAATAAAAATAAA | 7409 |
rs189721732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827050 | CACTGAACCCCAATT[C/T]CAACCAACCCCTGAT | 7409 |
rs189724033 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6794335 | TGGGGAGAGGAGAAT[A/T]CAGTGACTGAAGAGG | 7409 |
rs189731463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844997 | CTTTATTCAAAATGT[C/T]GATGTTTGTTCATCA | 7409 |
rs189732266 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770949 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 7409 |
rs189744948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824820 | CAGGCGTGAGCCACC[A/G]CACCTGGCCGGACCA | 7409 |
rs189752830 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820914 | CAGGGGACAGGCAGA[C/T]AAGCCAGACCAGGCC | 7409 |
rs189832986 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6814560 | CAGCTATTTATCTAT[A/G]TATTCTTTGGGAATT | 7409 |
rs189845553 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849216 | GAGTGATCATATACT[C/T]GGTAGTTTTTCAGCT | 7409 |
rs189979704 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6779847 | CCGGGCACGGTGACT[C/T]ACACCTGTAATTCCA | 7409 |
rs190008564 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6842024 | TGAGCTCGGGAGTTT[C/G]AGACCAGCCCGACCA | 7409 |
rs190069719 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798211 | GAACCTGGGAGGCGG[A/G]GGTTGCAGTGAGCGG | 7409 |
rs190082538 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6780157 | TAATAATAATAATAA[C/T]AACCTCATCCATGAA | 7409 |
rs190085968 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835252 | ACACACACACACGTA[C/T]TTTATTGAGAGAGGA | 7409 |
rs190086650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831745 | ACTGCTCTGTCCCCA[A/G]CTCCTAGCAGTGTCT | 7409 |
rs190111630 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802739 | GTGTTGTACAGAGGT[G/T]AGAGGCACAGACTTT | 7409 |
rs190111762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818491 | TTAGGCAAGATCCTG[C/T]CTCAGGACCATTGCA | 7409 |
rs190121758 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838048 | TTATTAGCTGGTGTT[C/G]TGCTGCAAGAAAGAG | 7409 |
rs190132307 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855031 | CCGATTCCAAGGAGT[A/G]GAATAGACTTCAAAT | 7409 |
rs190153505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785355 | TTTCTTTGTTTTAAC[A/G]GGGTCTCTGTCTATT | 7409 |
rs190156224 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6798373 | TGCCTGAAGCCTGTA[A/G]TCTCGCCCCTTTGGG | 7409 |
rs190162070 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814709 | TTCTTTCTTTCTTTC[C/T]TTCTTTCTTTCTTTC | 7409 |
rs190173684 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6832367 | GGCTGTCTTCATCCT[C/T]GGAATGCAGGGGTTG | 7409 |
rs190180787 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6849533 | GGCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAG | 7409 |
rs190228745 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774337 | GTTTCACCGTGTTAG[C/G]CAGGATGGTCTCGAT | 7409 |
rs190287335 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808912 | TAGCTAGGTGCTTGT[C/T]TCTGCTCCACACGGT | 7409 |
rs190329509 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6817175 | GCCTCAGCCTCCCAA[A/G]TAGCTGGGATTACAG | 7409 |
rs190334626 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795154 | AGTTTTCGTAACAAG[A/G]AGCCATACCCTGGCT | 7409 |
rs190370725 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6840902 | CTCCCACTTCAGCCT[C/T]GAGTAGCTGGGATTA | 7409 |
rs190418959 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6780632 | GCTGGAGTGCAATGA[C/T]GTGATCTCAGCTCAC | 7409 |
rs190529141 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | VAV1 | GRCh38.p7 | 19:6797952 | TTAAAAAAAAAAAAA[A/C]CAGCTATATTGACAT | 7409 |
rs190544986 | snp | C/T | 0.00193715 | 0.0310616 | intron-variant | VAV1 | GRCh38.p7 | 19:6853116 | GCTTACAGCCTCAGC[C/T]CCTTCCCATTGTGGA | 7409 |
rs190585611 | snp | C/T | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857539 | CAGACAAAGCCCCCT[C/T]ACCAATCACAGACAA | 7409 |
rs190611105 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6788284 | ATGGAAAATAGGGGG[G/T]TTGGCTTTCTGGTCA | 7409 |
rs190637641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817965 | TGCTGGGATTACAGG[C/T]ATGAGCCACCACGCC | 7409 |
rs190651642 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | VAV1 | GRCh38.p7 | 19:6853895 | TGTGCCCCCAGAGAG[G/T]GAGTGGGTATCTGCC | 7409 |
rs190782246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783040 | CATAAATTAGCCAGG[C/T]GTGGTGGTGTATGCC | 7409 |
rs190796556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813223 | AAGGCCTTAGCTGGA[A/G]GGTCTACTTCCTGAG | 7409 |
rs190805081 | snp | A/G | 0.00557542 | 0.0525036 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771915 | CAAAGATCAGGGCTT[A/G]ACCTAGGGAGGTGGG | 7409 |
rs190817131 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802536 | CCTCTTTGAGGCATC[A/T]CATGACTGGAAGGAA | 7409 |
rs190821258 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818158 | GGGGTCTCCCTGTGT[C/T]GACCAGGCTGGTCTT | 7409 |
rs190828054 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840462 | AGGCACTTGCCACCA[C/T]GCCTGGCTAATTTTT | 7409 |
rs190851113 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771517 | CCCAGCACTTTGGGA[G/T]GCTGAGGCGGGCGGA | 7409 |
rs190876328 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801177 | TCTGGTGCTTGGCAT[A/C]CAGTAGGCATTCCAC | 7409 |
rs191046226 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6774963 | TAGAGATGGGGTTTT[C/T]CCATGTTGACCAAGC | 7409 |
rs191050562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850051 | AATTTACAGTCCAGC[C/T]CACAGTGTAGAGGAA | 7409 |
rs191054952 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6805253 | AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 7409 |
rs191056899 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6792869 | TGGATAGAGGCCAGA[G/T]ATGCTTCTGAGTGTC | 7409 |
rs191103751 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6777936 | CTCCTGAGTATCTGG[A/G]ATTACAGGCGCCTGC | 7409 |
rs191114165 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806317 | GTCTCGAACTCCTGA[A/C]CTTGTGATTCACCCG | 7409 |
rs191132755 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6841078 | CCACCATGCCGGGCC[C/T]AATTTTTGTATTCTT | 7409 |
rs191179001 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797390 | AATTTATCTCTCATT[C/G]ACTATGTTTTATCAA | 7409 |
rs191342498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793641 | CACATCACAGCCTAT[A/G]ATTTGTATGATAACA | 7409 |
rs191358046 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772135 | AGAGCGAAGAGGCCC[A/G]TGTGGCTGGAGCACA | 7409 |
rs191361542 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6795594 | ACTGATGATACGTAA[C/T]GGTTTACTATGTCCT | 7409 |
rs191362301 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6822848 | ATATATAAATATATA[C/T]AAAGTATATATAAAA | 7409 |
rs191379781 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826548 | CAAGGCCAGGGCTGA[C/T]GCCAGCCTCTGCCCG | 7409 |
rs191383090 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6812454 | GAGGTAAGGAGTTCA[A/G]GACCAGCCTGGCCAA | 7409 |
rs191395078 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6831233 | GGCTCTTCCTTACTT[C/T]CTTCTGCTTTTTCTC | 7409 |
rs191404005 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848252 | CCTGCTGGTTCCCAC[C/G]TGCCTTTCACCTTCT | 7409 |
rs191419545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793320 | GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA | 7409 |
rs191423232 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | VAV1 | GRCh38.p7 | 19:6844835 | TCATTAAGGTCCATC[A/G]TGTTTTAATGCAACA | 7409 |
rs191460350 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6816316 | TGAGCCACCATGCCC[A/G]GCTACAAAAACATTT | 7409 |
rs191605177 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809927 | TGTAATACCAGCACT[A/T]TGGGAAGCCAAGACA | 7409 |
rs191624193 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6799593 | TTCTCCGAATGCTAT[C/T]CCTCTCCTAACCCCC | 7409 |
rs191624378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786294 | AAATGATAACTCATG[A/G]GCCCAAGCTGCCTCG | 7409 |
rs191625275 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789866 | GGCCTCCCAAAGTGC[A/T]GGATTACAGGCATGA | 7409 |
rs191639049 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | VAV1 | GRCh38.p7 | 19:6816510 | TCTCTCTCTCTCACA[C/T]GCACACAGACACATA | 7409 |
rs191647290 | snp | C/T | 0.000428266 | 0.014627 | intron-variant | VAV1 | GRCh38.p7 | 19:6833746 | AAGGTAAGACTTTCC[C/T]GTGGTCCTTCCTGTG | 7409 |
rs191652198 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851089 | TTAAATTTTACTTAC[A/G]TATATATACATATGT | 7409 |
rs191661796 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | VAV1 | GRCh38.p7 | 19:6776354 | TCCATCCACTCATCT[A/G]TCCATCCATCCATCC | 7409 |
rs191680931 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6782151 | CCTGTCCAACATGGC[A/G]AAAGCCCAACTCTAC | 7409 |
rs191696803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797008 | TTTGGGAGGCCGAGA[C/T]GGGTGGATCACTTGA | 7409 |
rs191720299 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6833073 | AAGCCAATCAATGAA[A/T]GAGTGGACACGCAAA | 7409 |
rs191831761 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839817 | CACTTCCGCCTCCCA[A/G]GTAGCTGGGACTACA | 7409 |
rs191838574 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6856648 | AGAATCACTTGAACC[C/T]GGGAGGTGGAGGTTG | 7409 |
rs191915705 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6837411 | TGCCTGTGTCCTTGC[C/T]CTGCTCCTGGTGGAC | 7409 |
rs191935483 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6786198 | ACCTGGCACATAGTA[C/T]GGAATCAATTAATTT | 7409 |
rs191944711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6799401 | TCTCGAACTCCTGAC[C/T]TCATAATCTGCCCAC | 7409 |
rs191972209 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6832492 | TCCTCCTCCTCCTCC[C/T]CTTTCTCCTTCTCCT | 7409 |
rs192127903 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798876 | ATCAATGGATCATAT[C/G]CATTGCCCCTCAAAG | 7409 |
rs192194573 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6790707 | AGCAGGGCTACCCCA[C/T]TGGCAGTGAGCCCAG | 7409 |
rs192216908 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819251 | AAATCTAAGAAGTTA[A/T]GTTTCTGAACCTATT | 7409 |
rs192236154 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6854449 | CAGTCACGGTGGCTC[A/T]TGCCTGTAATCCCAG | 7409 |
rs192265107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824346 | AACCACGAGCTTACT[C/T]GCTGTCTCTGTGGAT | 7409 |
rs192273033 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6841893 | GTTGATTTGTTTTTG[C/T]CTTATAGTAGCTGTC | 7409 |
rs192427912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855610 | CCACCATCCAGCCAA[C/T]ATCTATTCATCCATT | 7409 |
rs192479324 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773875 | GAACGGGGGACGGGG[C/T]GGGGCTGGTGGAGTC | 7409 |
rs192485901 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6791436 | GAGCTATCTCATCTC[A/G]AGGTCCTTGAGCTAG | 7409 |
rs192497617 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820313 | CCATCATAGCTCACC[A/G]CAGGCTCGAACTCCT | 7409 |
rs192499474 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6785948 | ACAGGTAATGAGCCA[C/G]CGCGCCCAGCCCAGA | 7409 |
rs192500567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839428 | TGCACCACCACACCT[C/G]GCTAATTTTTTGTAT | 7409 |
rs192510056 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815158 | TTATTTATTTATTTA[C/T]TTATTTTGAGACAGG | 7409 |
rs192527011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793840 | CAAATGGAGATAAAA[C/T]TAGTCCCTACCTTAT | 7409 |
rs192532946 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6806911 | GGAATGTGATGGTTG[A/G]TAAGAACTTGTTTCT | 7409 |
rs192542999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841624 | GGATTACAGGCATGC[A/G]TCACCACGCCCGGCT | 7409 |
rs192599469 | snp | A/C/G | 5.98741e-05 | 0.0054712 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772787 | CGAGGGTGCACGGCC[A/C/G]GCCCTGGGCAGGCGG | 7409 |
rs192605239 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803863 | AGCCACTGCTCCCAG[C/T]GCAGACAATGGAATA | 7409 |
rs192605392 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811375 | ATTGGGCACTATTGC[A/G]TGCCACCATGTGGTG | 7409 |
rs192630815 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838458 | CATCTATCTACTTAT[C/T]AATACATTCATGATC | 7409 |
rs192685550 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6808039 | AAAAAAAGGCCGGGC[A/G]CGGTGGCTCAAGCCT | 7409 |
rs192700175 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842184 | GCTGTGAGCCAAGAT[C/G/T]GCGCCATTGCACTCC | 7409 |
rs192727637 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6830279 | GGCCAGGATGGTCTC[A/G/T]ATCTCTTGACCCCGT | 7409 |
rs192842994 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6794238 | TCATTTATCAATGAG[G/T]GAAATCATTTGGGAC | 7409 |
rs192897218 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6794399 | AATTTCAGCATTCTG[G/T]GAGGCTGAGGCAGGA | 7409 |
rs192905589 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824992 | CCTTCCCCTGTCTCT[C/T]TGAGACTGGTCTGGA | 7409 |
rs192927418 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6811515 | GAGGCTGCAGTTGGG[C/G]GAGAATGAGGACTCT | 7409 |
rs192933290 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6847319 | GGCAGTTGCTCCTGC[C/T]TCCCGCAGCCCCCGG | 7409 |
rs193053978 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807472 | CTCAGGTGGTAATGC[A/G]AGCAATGGGGAGTGG | 7409 |
rs193068884 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781308 | CCAAATTGTTATCCG[C/T]CTGGGATTGTTTCCA | 7409 |
rs193075788 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6810501 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC | 7409 |
rs193104856 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800347 | TGGGGTCTTGCTCTG[C/T]TGCCCAGGCTGGAGT | 7409 |
rs193110254 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6835009 | GATCACGCCACTGCA[C/T]GCCAACCTGGGCAAC | 7409 |
rs193250042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6856042 | GCTTATGCCTGTAAT[C/T]CCAGCACTTTGGGAT | 7409 |
rs193256963 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6786458 | CACAGCAAGCCCGTC[C/T]CTGTAAAATAAATTA | 7409 |
rs193261739 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816981 | AAGGGTATAAACACT[A/G]ACAGTGTGGTTATGA | 7409 |
rs193266669 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852171 | GGCATGCACTGTCAT[G/T]CCTGGCTAATTGTTT | 7409 |
rs199610931 | snp | C/G | 0.000399281 | 0.0141238 | missense | VAV1 | GRCh38.p7 | 19:6772976 | CCCCATGCCATCAAC[C/G]TGCGTGAGGTCAACC | 7409 |
rs199624825 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788386 | ATTATTATTATTATT[A/T]TTTTGAGACTGAGTC | 7409 |
rs199634646 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838097 | TCTGTCTGTCTGTCT[A/G]TCTATCTATCTATCT | 7409 |
rs199637092 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852737 | AAGAAAAAAAAAAAA[-/G]AAAGAAAGAACCTGT | 7409 |
rs199644964 | snp | C/T | 9.27515e-05 | 0.00680934 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826627 | GTTCCTCGTCTATGG[C/T]CGCTACTGCAGCCAG | 7409 |
rs199645156 | in-del | -/TAA | 0.0494327 | 0.149241 | intron-variant | VAV1 | GRCh38.p7 | 19:6834602 | TAATAATTTATTATT[-/TAA]TAATATATTAATATT | 7409 |
rs199653383 | snp | A/G/T | 5.00013e-05 | 0.00499981 | intron-variant | VAV1 | GRCh38.p7 | 19:6850651 | CCAGACTCAGGGCCC[A/G/T]GTGACCATCTGGTTC | 7409 |
rs199673099 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845235 | AAAATACAAAAAAAA[A/T]TTAGCTGGGCATGGT | 7409 |
rs199700014 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814667 | CTTCCTTCCTTCCTT[C/T]CTTCCTTTCTTTCTT | 7409 |
rs199719830 | snp | C/T | 1.67806e-05 | 0.00289656 | intron-variant | VAV1 | GRCh38.p7 | 19:6852945 | CTGGGATAGCATCTG[C/T]CATGTGGTCCGCCTT | 7409 |
rs199743609 | in-del | -/AC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835248 | CACACACACACACAC[-/AC]GTATTTTATTGAGAG | 7409 |
rs199771346 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838335 | TATCTATCTATCTAT[A/C]TGTCTATCTATCCAT | 7409 |
rs199781915 | snp | A/G | 6.60251e-05 | 0.00574528 | missense | VAV1 | GRCh38.p7 | 19:6850749 | AAAAAGGCTTTCCGG[A/G]GGCTTACGGTAAGGG | 7409 |
rs199788005 | snp | A/G | 0.000132304 | 0.0081323 | missense | VAV1 | GRCh38.p7 | 19:6854097 | GGGAGATCTATGGCC[A/G]GGTGAGGCAGGCAGG | 7409 |
rs199795639 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852724 | AGACTCCGTCTCAAA[-/G]AAAAAAAAAAAAGAA | 7409 |
rs199798227 | snp | A/C/T | 0.000181896 | 0.00953504 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6833217 | GAATGCCACCGCCAA[A/C/T]GGGCATGACTTCCAG | 7409 |
rs199812545 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847180 | GCCTCCCAAAGTGCT[G/T]GGATTACAGGCGTGA | 7409 |
rs199829070 | snp | C/T | 1.64849e-05 | 0.00287092 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772930 | CCTCCGGGATGGTGT[C/T]CTTCTGTGTCAGCTG | 7409 |
rs199854905 | in-del | -/AATAATAAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780113 | AAGACTCTGTCTTAA[-/AATAATAAT]AATAATAATAATAAT | 7409 |
rs199977948 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800135 | GGCTCTGTTTCTTAA[-/T]TTTTTTTTTTTAATA | 7409 |
rs199986946 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832562 | CTTCCTCCTCCTCTC[C/T]TTCCTCCCCTTCCTC | 7409 |
rs200027004 | snp | G/T | 0.0912534 | 0.193131 | intron-variant | VAV1 | GRCh38.p7 | 19:6809086 | ACCTCTCTTTTTTTT[G/T]TTTTTTTTTTTTGAG | 7409 |
rs200027879 | in-del | -/GA | 0.0267878 | 0.112589 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771970 | GCTGTGATTTGAAAT[-/GA]GGGGATTTAGGAAGA | 7409 |
rs200036501 | in-del | -/TA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851343 | ATGCCTGGCTAATTT[-/TA]AAAAAAAATTTTTTT | 7409 |
rs200040951 | in-del | -/CG | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6817717 | TCTGAGATGGGGTCT[-/CG]CTCTGTTGCCCAGGC | 7409 |
rs200066793 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786300 | TAACTCATGGGCCCA[A/G]GCTGCCTCGTGTTTT | 7409 |
rs200072158 | snp | C/T | 0.00817076 | 0.0633926 | intron-variant | VAV1 | GRCh38.p7 | 19:6833972 | AGTTGGCAGGGGTTG[C/T]TGTGTGGGGGCAGGA | 7409 |
rs200086086 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800638 | GTTTTTTGTTTTTTT[-/T]GAGACATCCTCGGTC | 7409 |
rs200101082 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809101 | TTTTTTTTTTTTTGA[G/T]ATAGGGTCTTGTCTT | 7409 |
rs200146364 | snp | C/G/T | 3.29855e-05 | 0.00406102 | intron-variant | VAV1 | GRCh38.p7 | 19:6821593 | GGGGTGTACAAGGGG[C/G/T]TCACTGAGTGGCCAC | 7409 |
rs200164438 | snp | G/T | 0.000115339 | 0.00759318 | intron-variant | VAV1 | GRCh38.p7 | 19:6825043 | TCATCTTTCTCTCCC[G/T]TCCCCGCAGCATTTC | 7409 |
rs200232544 | snp | C/T | 8.31995e-05 | 0.00644925 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848055 | GGCCAACCGCTCGGA[C/T]GGGACTTTCTTGGTG | 7409 |
rs200248407 | in-del | -/C | 0.417521 | 0.185571 | intron-variant | VAV1 | GRCh38.p7 | 19:6780065 | GCAGTGAGCCGAGAT[-/C]AGGCCACTGCACTCC | 7409 |
rs200254050 | snp | C/G/T | 0.000148954 | 0.00862871 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833211 | TCCGGAGAATGCCAC[C/G/T]GCCAACGGGCATGAC | 7409 |
rs200297873 | in-del | -/AAG | 0.0726307 | 0.176182 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771462 | CTCAAAAGAAAAAAA[-/AAG]AAGAAAGAAGCCTGG | 7409 |
rs200320698 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800328 | TCATTTTTTTTTTTT[G/T]AGATGGGGTCTTGCT | 7409 |
rs200332893 | snp | A/G | 0.00067859 | 0.0184075 | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6822447 | AGTATGACAAGCGCT[A/G]CTGCTGCCTGCGGGA | 7409 |
rs200346713 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796354 | ATGGGGTGCTTGGGG[-/T]GACAGCCACTTGCTG | 7409 |
rs200361477 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841478 | TACTATTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 7409 |
rs200369996 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843100 | GTCAAGCTGGGGTCT[C/T]TACACTAAGTTGGGG | 7409 |
rs200370198 | in-del | -/CT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832596 | CTCGCCCTCCTCTTC[-/CT]CTTCCTCCTATTCCT | 7409 |
rs200372510 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776163 | TCATCTATCCACCCA[C/T]CCATCCATCCATCCA | 7409 |
rs200485277 | in-del | -/A | 0.0547245 | 0.156101 | intron-variant | VAV1 | GRCh38.p7 | 19:6802091 | AACTATAGCAAGGAC[-/A]AAAAAACCAAACACC | 7409 |
rs200496717 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790183 | ACTCTGTCTCAAAAA[A/T]AAAATAAAATAAAAT | 7409 |
rs200511030 | snp | A/G | 4.94792e-05 | 0.00497365 | intron-variant | VAV1 | GRCh38.p7 | 19:6820866 | TTTCAGTTAATTTCT[A/G]TTGACGTCTACACTG | 7409 |
rs200528024 | snp | C/T | 6.59141e-05 | 0.00574045 | intron-variant | VAV1 | GRCh38.p7 | 19:6828766 | GGGAGAGTGTGTGTC[C/T]GGCTCCTTTCTTGGG | 7409 |
rs200540807 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799376 | GGTTTCACCATGTTG[A/G]CCAGGCTGGTCTCGA | 7409 |
rs200551288 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850135 | TGTGAATTTCCCTTA[-/C]CTTTTTTTTTTTTTG | 7409 |
rs200574586 | snp | C/G | 1.6477e-05 | 0.00287024 | intron-variant | VAV1 | GRCh38.p7 | 19:6825029 | AATCTTATCTTCCGT[C/G]ATCTTTCTCTCCCTT | 7409 |
rs200588507 | snp | A/G | 0.000131885 | 0.00811942 | intron-variant | VAV1 | GRCh38.p7 | 19:6833653 | GGGAGGCTGGGAGGT[A/G]AGCTTGGTTCTCTTT | 7409 |
rs200590105 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838337 | TCTATCTATCTATAT[A/G]TCTATCTATCCATGT | 7409 |
rs200632319 | snp | C/T | 0.000379353 | 0.0137671 | intron-variant | VAV1 | GRCh38.p7 | 19:6857041 | CACTGATGAACTCCT[C/T]GTCTGTTTCCAGGTT | 7409 |
rs200685316 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6780694 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAT | 7409 |
rs200700855 | snp | A/G | 0.000197928 | 0.00994611 | intron-variant | VAV1 | GRCh38.p7 | 19:6821575 | AAGCTGTGTTCTGCC[A/G]TGGGGGTGTACAAGG | 7409 |
rs200702921 | in-del | -/ACACACACACACAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835215 | TATATATATATACAT[-/ACACACACACACAC]ACACACACACACACA | 7409 |
rs200705988 | snp | C/T | 0.000263631 | 0.0114781 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828099 | TCAGAGAGCCAACAA[C/T]GGGAGGTTCACCCTG | 7409 |
rs200808224 | in-del | -/ATCCATCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838433 | TCCATCCATCCATCC[-/ATCCATCT]ATCATCTATCTACTT | 7409 |
rs200833165 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805615 | ACACACACACACACA[C/T]ACACGCACACACACA | 7409 |
rs200840526 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | VAV1 | GRCh38.p7 | 19:6774421 | GTGTGAGCCACCGCG[C/T]CCAGCCTTTTTTTTT | 7409 |
rs200851743 | snp | A/G | 8.24654e-05 | 0.00642074 | intron-variant | VAV1 | GRCh38.p7 | 19:6828743 | TGGGCCAGGGGTGTG[A/G]CCACGTGGGGAGAGT | 7409 |
rs200899240 | snp | C/T | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6826581 | CTTGATGCCAGTCAC[C/T]TTTACCTGGTGGCCT | 7409 |
rs200915324 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6832638 | TTCTTCCTCCTCCTC[C/T]CTTTCCTCCCCTTCT | 7409 |
rs200950048 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856699 | ATTGCACTCCAGCCT[A/G]GGGGGCAGAGTGAGA | 7409 |
rs200951046 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856191 | AATCCCAGGTACTCG[C/T]TAAGCTGAGGCAGGA | 7409 |
rs200967463 | in-del | -/TTTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774123 | ACTCCTTCTGTTTAT[-/TTTA]TTTATTTATTTATTT | 7409 |
rs201002344 | snp | A/G | 0.00034457 | 0.0131212 | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6822510 | CGCTGGGCTCCATCC[A/G]GCAGGTGGGCGCCTC | 7409 |
rs201027298 | in-del | -/A/AA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793333 | GCGAGACTCCATCTC[-/A/AA]AAAAAGAAAGAAAGA | 7409 |
rs201028318 | in-del | -/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771790 | AGAAAGGAAAGAAAG[-/G]AAAGGAAGGAAGGAA | 7409 |
rs201047195 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795784 | CGCCTCCTGGGTTCA[A/T]GTGATTCTCCTGTCT | 7409 |
rs201079372 | snp | A/G | 4.48722e-05 | 0.00473646 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822275 | GGAGAATGAGGAGGC[A/G]GAAGGCGACGAGATC | 7409 |
rs201171114 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852720 | GCCAGACTCCGTCTC[-/A]AAAGAAAAAAAAAAA | 7409 |
rs201171550 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809097 | TTTTTTTTTTTTTTT[G/T]TGAGATAGGGTCTTG | 7409 |
rs201184602 | snp | C/T | 0.0029955 | 0.0385847 | intron-variant | VAV1 | GRCh38.p7 | 19:6833151 | TAAAATACTGACCTT[C/T]TTTTTTTTTTTTTTT | 7409 |
rs201188879 | in-del | -/TCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832726 | TCCTCTTCTTCCTTT[-/TCC]TCCTCCTCCTTCTTC | 7409 |
rs201244174 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | VAV1 | GRCh38.p7 | 19:6790184 | CTCTGTCTCAAAAAT[A/G]AAATAAAATAAAATA | 7409 |
rs201252235 | snp | A/C/T | 0.000709513 | 0.0188218 | intron-variant | VAV1 | GRCh38.p7 | 19:6832207 | GATGGCCATGTGAGT[A/C/T]CCCGTCTTCCTCCCT | 7409 |
rs201259230 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796256 | GAGTGTGTACTCGAG[-/A]GAGAGGTGGGAGAAA | 7409 |
rs201336552 | snp | A/T | 6.59076e-05 | 0.00574016 | intron-variant | VAV1 | GRCh38.p7 | 19:6837077 | AAGTCTGAATGGAAT[A/T]AGGGCAAGGGGTCCA | 7409 |
rs201339418 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850822 | CCTCCCTGCACCTCC[A/G]CCTTGGGACCCCCTT | 7409 |
rs201409833 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771828 | AAGGAAGGAAGGAAG[A/G]AAGGAAGGGAGGGAA | 7409 |
rs201468135 | snp | C/T | 0.000695042 | 0.018629 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825323 | GCTTCGTGTTCATAC[C/T]CACTTCCTAAAGGAG | 7409 |
rs201487888 | in-del | -/CTCTCA | 0.151334 | 0.229706 | intron-variant | VAV1 | GRCh38.p7 | 19:6816505 | GCTCTCTCTCTCTCT[-/CTCTCA]CACACGCACACAGAC | 7409 |
rs201489097 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844063 | TTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 7409 |
rs201498576 | snp | C/T | 4.99255e-05 | 0.00499603 | intron-variant | VAV1 | GRCh38.p7 | 19:6848162 | GGGGCCTGGGCCCTG[C/T]GGGCCTGGGAAAAAG | 7409 |
rs201509178 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809098 | TTTTTTTTTTTTTTT[A/T]GAGATAGGGTCTTGT | 7409 |
rs201520206 | snp | C/G | 3.30513e-05 | 0.00406504 | intron-variant | VAV1 | GRCh38.p7 | 19:6821702 | AACCACCTGGGCCTT[C/G]GGCCATTTAGCCCCA | 7409 |
rs201530612 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6820666 | CTCCCCTGCCCTTTC[A/G]TACTGCCCCACCCTC | 7409 |
rs201546460 | in-del | -/AC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852722 | CAGACTCCGTCTCAA[-/AC]AGAAAAAAAAAAAAG | 7409 |
rs201607630 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816913 | AAGTTGCAGTGAGCC[A/G]AGATGGTGCCACTGC | 7409 |
rs201612754 | in-del | -/AAAGA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799869 | AAAAAAAAAAAAAGG[-/AAAGA]AAAGAAAACAGAATC | 7409 |
rs201617377 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832560 | TTCTTCCTCCTCCTC[-/T]CCTTCCTCCCCTTCC | 7409 |
rs201627485 | snp | A/C/G | 0.000148337 | 0.00861106 | intron-variant | VAV1 | GRCh38.p7 | 19:6833980 | GGGGTTGCTGTGTGG[A/C/G]GGCAGGAGGAAAATT | 7409 |
rs201637015 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851340 | ATCATGCCTGGCTAA[-/T]TTTAAAAAAAAATTT | 7409 |
rs201671381 | snp | A/G | 1.64955e-05 | 0.00287184 | intron-variant | VAV1 | GRCh38.p7 | 19:6857042 | ACTGATGAACTCCTC[A/G]TCTGTTTCCAGGTTG | 7409 |
rs201831100 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | VAV1 | GRCh38.p7 | 19:6804082 | TTAGTGGAAAGGGGG[A/G]ATGGATAGGCAGAGC | 7409 |
rs201838603 | in-del | -/ATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777235 | TTTATCTGTTTAACT[-/ATCC]ATCCATCCATCCATC | 7409 |
rs201843981 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832560 | TTCTTCCTCCTCCTC[C/T]CCTTCCTCCCCTTCC | 7409 |
rs201859931 | in-del | -/ACACACACACACACACACAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836834 | TGAGCAGAGAGATGG[-/ACACACACACACACACACAC]ACACACACACACACA | 7409 |
rs201872764 | in-del | -/TTTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848416 | TTTCTTTTCTTTTCT[-/TTTC]TTTTTTTTTCTGACA | 7409 |
rs201920803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6785665 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTGAG | 7409 |
rs201926382 | snp | A/C/G/T | 0.0018697 | 0.0305195 | intron-variant | VAV1 | GRCh38.p7 | 19:6821727 | GCCCCAGTCCTCCCC[A/C/G/T]TCCCTGAAGCCCCAC | 7409 |
rs201935967 | in-del | -/TC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785663 | CTTTCTTTCTTTCTT[-/TC]TTTTTTTTTTTTTTG | 7409 |
rs202005344 | in-del | -/TATCTATC | 0.0681886 | 0.171594 | intron-variant | VAV1 | GRCh38.p7 | 19:6838296 | TCGTCATCTACATAT[-/TATCTATC]TATCTATCTATCTAT | 7409 |
rs202022620 | in-del | -/AATT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786205 | ACATAGTACGGAATC[-/AATT]AATTTATTCATTTAT | 7409 |
rs202028662 | in-del | -/C | 0.0810805 | 0.184299 | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857556 | CAATCACAGACAAAG[-/C]CCCCTCACCAATCCA | 7409 |
rs202031133 | in-del | -/ATCCATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838393 | TCAATCAGTTCTTCT[-/ATCCATCC]ATCCATCCATCCATC | 7409 |
rs202083007 | snp | A/G | 1.67464e-05 | 0.0028936 | intron-variant | VAV1 | GRCh38.p7 | 19:6825130 | CATTGAGGTGAGCCG[A/G]CCGATCCCCAGCCCT | 7409 |
rs202088049 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780573 | TTTTCTTTCTTTTTT[C/T]TTTTTTTTTTTTTTT | 7409 |
rs202101579 | in-del | -/TTTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785641 | TGGTCAGTGGCCAGG[-/TTTC]TTTCTTTCTTTCTTT | 7409 |
rs202103820 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819119 | GACTCCATCCCCCTC[-/A]AAAAAAAAGAAAGAA | 7409 |
rs202111007 | snp | C/G | 0.000791504 | 0.0198778 | intron-variant | VAV1 | GRCh38.p7 | 19:6828494 | GCCATGAGGGTGAGT[C/G]GGTGTAGGGTGCTGG | 7409 |
rs202159280 | snp | A/C | 1.64792e-05 | 0.00287042 | intron-variant | VAV1 | GRCh38.p7 | 19:6828806 | CTAGACCCCCTGCCT[A/C]CTGCATAGGACCAGT | 7409 |
rs202178080 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835218 | ATATATATACATACA[C/T]ACACACACACACACA | 7409 |
rs202196036 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814439 | TGTAGGATTTCACAA[-/T]TTTTTTTTTTAATTT | 7409 |
rs202203908 | in-del | -/TTT | 0.298144 | 0.245321 | intron-variant | VAV1 | GRCh38.p7 | 19:6784494 | ATTCCATTCTGTTCC[-/TTT]TTTTTTTTTTTTTTT | 7409 |
rs202232330 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848746 | TATATATGTTTTTTC[-/T]TTTTTTTTTAACTTC | 7409 |
rs267605753 | snp | A/G | | | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828877 | CAAGATCACCTCGGT[A/G]GAACGGCGCTCCAAG | 7409 |
rs267605754 | snp | A/G | | | missense | VAV1 | GRCh38.p7 | 19:6850713 | ATCATGACAGCAGAA[A/G]GACTGTACCGGATCA | 7409 |
rs367566378 | snp | A/G | 0.000307953 | 0.0124049 | intron-variant | VAV1 | GRCh38.p7 | 19:6825164 | GGGTCTGTCTAGTGC[A/G]GATAACCTGCTGCCC | 7409 |
rs367576818 | snp | A/G | 8.33604e-05 | 0.00645548 | intron-variant | VAV1 | GRCh38.p7 | 19:6833317 | AGGGTCCTGCATACC[A/G]GACTTGGTCATCAGT | 7409 |
rs367627295 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792446 | AGCTTAGGGACTTGC[A/G]TGAATTAGGGTATCT | 7409 |
rs367644250 | snp | C/T | 3.31318e-05 | 0.00406999 | intron-variant | VAV1 | GRCh38.p7 | 19:6837096 | GCAAGGGGTCCAGGG[C/T]GGGTCCTGGGAGGAT | 7409 |
rs367673889 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810827 | TGAAGAGGCTGGAGG[C/G]AGAGCAAGTTTGAAC | 7409 |
rs367751785 | snp | G/T | 0.000159987 | 0.00894248 | intron-variant | VAV1 | GRCh38.p7 | 19:6826737 | GGCCACTTCTCGGGG[G/T]CCTCTCCCGCTCCTC | 7409 |
rs367773643 | in-del | -/CTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832670 | CTCCTCCTCCTCCTC[-/CTC]TTCCTCCTCTTCTTT | 7409 |
rs367830862 | snp | C/T | 1.71838e-05 | 0.00293114 | intron-variant | VAV1 | GRCh38.p7 | 19:6828221 | ACCTACTCTCCTGTG[C/T]CTATAAAAGTGGGGA | 7409 |
rs367861307 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776521 | ATCCATCCATCCTCT[-/CATC]CATCCATCCATCCAT | 7409 |
rs367877255 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6842338 | TTTTCTGTAAAGAGC[A/C]GAAGAGTAGTGTAAA | 7409 |
rs367877437 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784220 | GATTGTGCTACCACT[A/G]TACTCCAGACTGGAC | 7409 |
rs367880755 | snp | A/T | 1.65315e-05 | 0.00287498 | intron-variant | VAV1 | GRCh38.p7 | 19:6821707 | CCTGGGCCTTGGGCC[A/T]TTTAGCCCCAGTCCT | 7409 |
rs367945407 | snp | C/T | 6.7104e-05 | 0.00579202 | intron-variant | VAV1 | GRCh38.p7 | 19:6836606 | TGATGGGGTGGGACC[C/T]AAGTGTAGGGTTATG | 7409 |
rs367963535 | snp | C/T | 0.000649908 | 0.0180148 | intron-variant | VAV1 | GRCh38.p7 | 19:6825292 | CAGCCCTCACCCTTC[C/T]CTCCGAGTAGGACCT | 7409 |
rs367965223 | snp | A/G | 9.71487e-05 | 0.00696885 | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6822444 | CAGAGTATGACAAGC[A/G]CTGCTGCTGCCTGCG | 7409 |
rs367969068 | snp | A/G | 0.000534712 | 0.0163423 | intron-variant | VAV1 | GRCh38.p7 | 19:6833498 | CTGTAAAGGTCACTC[A/G]CTCTTCTTTATGTGT | 7409 |
rs367973362 | snp | A/G/T | 4.4692e-05 | 0.00472698 | intron-variant | VAV1 | GRCh38.p7 | 19:6833133 | TTCAGCCATAAAAAG[A/G/T]AATAAAATACTGACC | 7409 |
rs367993949 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809612 | GTGAGGTTGAACTTT[A/G]TGTTGGGGATGATGG | 7409 |
rs368068443 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797491 | GCGGATCATCTGAGG[G/T]TGGGAGTTCGAGACT | 7409 |
rs368118884 | snp | A/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771496 | GCGGTGGCTCACGCC[A/T]GTAATCCCAGCACTT | 7409 |
rs368143016 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823130 | CTTTATCTATCTATC[-/TT]TTTTTTTTTTTTGAG | 7409 |
rs368272156 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6818882 | GCACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 7409 |
rs368328179 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795349 | GAGCAAATGACCCTC[C/G]TTCTCTGAACTCTGT | 7409 |
rs368374146 | snp | C/T | 3.32441e-05 | 0.00407688 | missense | VAV1 | GRCh38.p7 | 19:6825117 | TCATCTTTATCAACA[C/T]TGAGGTGAGCCGGCC | 7409 |
rs368378556 | snp | A/G | 1.65773e-05 | 0.00287895 | intron-variant | VAV1 | GRCh38.p7 | 19:6833297 | TTAGGTGAGAATCTG[A/G]GAGGAGGGTCCTGCA | 7409 |
rs368386793 | in-del | -/A | 0.0126979 | 0.078662 | intron-variant | VAV1 | GRCh38.p7 | 19:6816167 | TGGGACTACAGGCGC[-/A]CACCACCACGCCCAG | 7409 |
rs368405546 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810019 | CTACAAAAAATAAAA[A/G]TAAAAATAACGTTAT | 7409 |
rs368409126 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815073 | GTCAGAGCCTTGGGC[A/G]AGCAACAGAATCTAC | 7409 |
rs368424950 | snp | A/G | 0.000165544 | 0.0090964 | intron-variant | VAV1 | GRCh38.p7 | 19:6848150 | TCATACCCTTTTGGG[A/G]CCTGGGCCCTGCGGG | 7409 |
rs368453923 | snp | C/G | 3.31066e-05 | 0.00406844 | intron-variant | VAV1 | GRCh38.p7 | 19:6850663 | CCCGGTGACCATCTG[C/G]TTCCAGATATAACGT | 7409 |
rs368465654 | snp | C/T | 3.29538e-05 | 0.00405904 | intron-variant | VAV1 | GRCh38.p7 | 19:6820831 | AAGGTGAGCTGCACA[C/T]TTGAAGCCCAAAGAC | 7409 |
rs368468307 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790140 | CTGAGATCGTGCAAG[C/T]GCACTCCAGCCTGGG | 7409 |
rs368533641 | snp | C/T | 0.000176351 | 0.00938853 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826693 | CGCAGCCCGGGAGGA[C/T]GTGCAGATGAAGCTG | 7409 |
rs368564136 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6807434 | AGGATCTAACGCTGC[A/T]GCTGATCTGACAGGA | 7409 |
rs368566937 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790297 | GTTACAGCACAGGAC[A/G]TAATGGACACAGTTA | 7409 |
rs368628133 | snp | A/G | 4.57195e-05 | 0.00478097 | missense | VAV1 | GRCh38.p7 | 19:6822285 | GAGGCGGAAGGCGAC[A/G]AGATCTATGAGGACC | 7409 |
rs368646952 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775447 | AAATACAGTCCTAAT[C/G]CTCTGTAACAGGGAA | 7409 |
rs368778356 | in-del | -/TCTCAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816506 | CTCTCTCTCTCTCTC[-/TCTCAC]ACACGCACACAGACA | 7409 |
rs368800375 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6839143 | CCTGACCTTGTGATC[C/T]GCCAGCTTCAGCCTC | 7409 |
rs368850087 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817841 | ACAGGCACCCGCCAC[C/T]TTGCCTGGCTAATTT | 7409 |
rs368911059 | snp | G/T | 0.000153988 | 0.00877328 | intron-variant | VAV1 | GRCh38.p7 | 19:6833660 | TGGGAGGTGAGCTTG[G/T]TTCTCTTTGGAGGAT | 7409 |
rs368912217 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6804747 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 7409 |
rs368935436 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816075 | CCCAGGCTGGAGTGC[A/G]GTGGCGCAATCTCGG | 7409 |
rs368996579 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799584 | ATTAGGTATTTCTCC[A/G]AATGCTATCCCTCTC | 7409 |
rs369064064 | snp | C/T | 0.000220983 | 0.0105092 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772786 | GCGAGGGTGCACGGC[C/T]GGCCCTGGGCAGGCG | 7409 |
rs369088086 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809283 | CTTGCTTTGTTGCCA[A/G]GCTGGTCTTGAACTC | 7409 |
rs369098962 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834821 | ACATATAAATATATA[A/G]CATAAGTCAGGTGTG | 7409 |
rs369136982 | in-del | -/GAGAGCTCAGCAA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850150 | ACTTTTTTTTTTTTT[-/GAGAGCTCAGCAA]TTTTTTTCTCAACAT | 7409 |
rs369162990 | snp | A/G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813355 | CCAAAATGGAGCTTC[A/G/T]ATATGTTTCATTATT | 7409 |
rs369165133 | snp | A/G | 9.88403e-05 | 0.00702925 | intron-variant | VAV1 | GRCh38.p7 | 19:6833681 | TTTGGAGGATTTCCC[A/G]TTCTCACCATTTCCT | 7409 |
rs369174552 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806296 | TTCACCATGTTGGTC[C/T]GGCTGGTCTCGAACT | 7409 |
rs369199419 | in-del | -/TGTGTGTGTG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831871 | GTGTGTGTGTGTGTG[-/TGTGTGTGTG]CATGTGCACGCCTGC | 7409 |
rs369229183 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778071 | CCTCCTGAGTAGCTG[A/G]GGCTACAGATGCGTG | 7409 |
rs369229287 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6778637 | CTACCCGAGAGGCTA[A/C]GTGGGGAGGATCACT | 7409 |
rs369264328 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777532 | TGACATTGCAGCAGA[C/G]ACCTGGGGAAAATTA | 7409 |
rs369298193 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6799316 | GGGACTACAGGTGTG[C/T]GCCACCACGCCTGGC | 7409 |
rs369300455 | snp | C/G | 1.64931e-05 | 0.00287163 | intron-variant | VAV1 | GRCh38.p7 | 19:6820672 | TGCCCTTTCGTACTG[C/G]CCCACCCTCATTTCT | 7409 |
rs369347874 | snp | A/G/T | 0.000164805 | 0.00907631 | intron-variant | VAV1 | GRCh38.p7 | 19:6843210 | ATGAGAGGTTTCTGG[A/G/T]TTGGGGTTCCAGGCT | 7409 |
rs369424348 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787238 | TGGAGTGCAGTGGTG[C/T]GATCTTGGCTCACTG | 7409 |
rs369425541 | in-del | -/TTGT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827605 | TGTTTGTTTGTTTGT[-/TTGT]CTTTGTTTTTTGAGA | 7409 |
rs369471383 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | VAV1 | GRCh38.p7 | 19:6817880 | TTTAGTAGAGACGGG[A/G]TTTCACCGTGTTAGC | 7409 |
rs369516080 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791333 | ATTTCCTCATCTCGA[G/T]GTCCTTGAGATAACT | 7409 |
rs369525815 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779980 | GCCGGGCGTGGTTGC[A/G]GGCGCCTGTAGTCCC | 7409 |
rs369579917 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6818728 | AGTAAACTAGGGTGC[A/G]GGCAGGGCAAGACCA | 7409 |
rs369673425 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805583 | CCTCATTTCTACAGA[C/T]ACACACACACACACA | 7409 |
rs369683699 | snp | A/G | 1.64868e-05 | 0.00287109 | intron-variant | VAV1 | GRCh38.p7 | 19:6829769 | GCCAGACAGGAATGC[A/G]TTATCCATCCTTCCA | 7409 |
rs369713533 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805872 | GGAAGGAAGGAAGAT[C/G]AGCCTGGAGTCTCTG | 7409 |
rs369715140 | snp | G/T | 0.000101058 | 0.00710765 | intron-variant | VAV1 | GRCh38.p7 | 19:6853087 | GCCAGCAGGTAGGAG[G/T]TCTCAGACTGGGGGC | 7409 |
rs369739561 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816474 | CCTGGACAACAGAGT[A/G]AGAGCATCTCTCTCT | 7409 |
rs369740531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785306 | CCTCCCAAAGTGCTC[A/G]GATACAGACATGAGC | 7409 |
rs369751737 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787974 | CCCAGCTACTTGGGA[A/G]GCTGAGGCAGGAGAA | 7409 |
rs369752331 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852487 | AGCACTTTGGGAGGC[C/T]GAGGCAGGCGGATCA | 7409 |
rs369789260 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795495 | ATTTATTTATTTATT[G/T]AATTAATTTTATTTA | 7409 |
rs369789463 | snp | A/G | 1.65165e-05 | 0.00287367 | intron-variant | VAV1 | GRCh38.p7 | 19:6857016 | GCAGTAGGAGGATGT[A/G]CAGAGGTTGCACTGA | 7409 |
rs369796904 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant | VAV1 | GRCh38.p7 | 19:6821866 | CCAGATCGAGTGAGT[A/G]CTCAGGCCTGTGGCC | 7409 |
rs369821298 | snp | A/T | 0.000437904 | 0.0147905 | intron-variant | VAV1 | GRCh38.p7 | 19:6824999 | CTGTCTCTCTGAGAC[A/T]GGTCTGGAGGAGGGA | 7409 |
rs369822794 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784865 | CTTTCAGGACTTTCA[C/T]AGAGATGCTAGAAAT | 7409 |
rs369840682 | snp | C/G | 1.6501e-05 | 0.00287232 | intron-variant | VAV1 | GRCh38.p7 | 19:6828596 | CGGCTGTTGGGGGGC[C/G]AGGTTCACCCCTGCC | 7409 |
rs369854343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816943 | CCCTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC | 7409 |
rs369854888 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841947 | GTGAGCACTTTCGGC[C/T]GGGCGCGGTGGTTCA | 7409 |
rs369914617 | in-del | -/CTTTCTTTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785653 | CAGGTTTCTTTCTTT[-/CTTTCTTTC]TTTTTTTTTTTTTTT | 7409 |
rs369931096 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808401 | CTTGGGTCATCCTTG[A/G]CAAACTAGGAGGTAA | 7409 |
rs369935797 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6780502 | CCTAGCTACAAACCC[A/G]TACAGCATGGGACTG | 7409 |
rs369979109 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782882 | AGTGAGATCCTGTCT[C/T]GGAAGAAAAAAAAAA | 7409 |
rs370008216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825863 | AACCCCGTCTCCATC[A/G]CCTAAAAATACAACT | 7409 |
rs370095317 | snp | C/T | 3.36084e-05 | 0.00409915 | intron-variant | VAV1 | GRCh38.p7 | 19:6821901 | AGCTCACTGGAGCAC[C/T]GTCCTGGGGGTGGAG | 7409 |
rs370151158 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809507 | TGCATTTAGCGTGTG[A/G]CAACCACTTCCACCT | 7409 |
rs370157494 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772150 | GTGTGGCTGGAGCAC[A/G]GTGAAGAGGGGGAGA | 7409 |
rs370175217 | snp | A/G | 9.94415e-05 | 0.00705059 | intron-variant | VAV1 | GRCh38.p7 | 19:6773051 | CTGAGGGTTGGAGAC[A/G]GGGGTCCTCCCCGGG | 7409 |
rs370181480 | snp | G/T | 0.00204129 | 0.0318823 | intron-variant | VAV1 | GRCh38.p7 | 19:6832054 | TCCCACCCTCTGCGG[G/T]GGCAGTGCCTTCAGT | 7409 |
rs370198449 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6774958 | TTTAGTAGAGATGGG[A/G]TTTTCCCATGTTGAC | 7409 |
rs370227615 | snp | A/G/T | 4.99907e-05 | 0.00499933 | intron-variant | VAV1 | GRCh38.p7 | 19:6854123 | GCAGGGCTGGGTGAC[A/G/T]GGGAGGGCATGGGGG | 7409 |
rs370229454 | in-del | -/TTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800626 | CTTTTTTTTGTTTTG[-/TTTT]GTTTTTTGTTTTTTT | 7409 |
rs370259540 | snp | C/T | 1.66101e-05 | 0.0028818 | intron-variant | VAV1 | GRCh38.p7 | 19:6836426 | CTCCTGTACCCTGTC[C/T]TCCAGGTCTGCCCAA | 7409 |
rs370303171 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817618 | TAAACACAACAAGAG[A/G]AGCAAAACTAAGGGG | 7409 |
rs370321152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807177 | GGATGATTCAAATGC[A/G]TTACATTTATTGTTC | 7409 |
rs370452515 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780597 | TTTTTTTTGGGACGG[A/C]GTCTCACTCTATTCC | 7409 |
rs370554352 | in-del | -/TTC | 0.308661 | 0.24302 | intron-variant | VAV1 | GRCh38.p7 | 19:6785662 | TCTTTCTTTCTTTCT[-/TTC]TTTTTTTTTTTTTTT | 7409 |
rs370571831 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6825500 | CAGACACCACTGGAC[A/G]GGGAGGACTTTTTGC | 7409 |
rs370586875 | snp | C/T | 0.000241072 | 0.0109762 | missense | VAV1 | GRCh38.p7 | 19:6848008 | TGCAGGTACGCAGGC[C/T]CCATGGAGCGGGCAG | 7409 |
rs370597762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840243 | TGTGTCTAGCTTGTT[C/T]CACTTGGCATAATGT | 7409 |
rs370624141 | in-del | -/ACAC/ACACACAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805583 | CTCATTTCTACAGAT[-/ACAC/ACACACAC]ACACACACACACACA | 7409 |
rs370716087 | snp | C/T | 0.000148249 | 0.00860829 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6820770 | CGGCCTCAAGCGGAG[C/T]GAGCTCTTCGAAGCC | 7409 |
rs370726079 | snp | C/T | | | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772828 | GCTGTGGCGCCAATG[C/T]ACCCACTGGCTCATC | 7409 |
rs370731016 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | VAV1 | GRCh38.p7 | 19:6775692 | GTGTCTGGTATGTAG[C/T]GGGGACGTGTGAGGG | 7409 |
rs370736596 | snp | C/G/T | 0.000280089 | 0.0118309 | intron-variant | VAV1 | GRCh38.p7 | 19:6825048 | TTTCTCTCCCTTCCC[C/G/T]GCAGCATTTCTTGAA | 7409 |
rs370749452 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826234 | TCCCAGCTACTCGGG[A/G]GGCTGAAGCAGGAGA | 7409 |
rs370757033 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6847809 | GTAGAAGTGGAAGCC[C/T]GCTCCCCATGTCTGG | 7409 |
rs370798699 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780856 | TGGGATTACACGTGA[G/T]AGCCACCATGCCCAG | 7409 |
rs370802899 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797319 | TCCCTTTGCTTGGAG[A/C]CTTTTTACCCCCTTC | 7409 |
rs370879228 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854599 | CGTGGTAGTGTGTCC[C/T]AGGTACTCAGGAAGC | 7409 |
rs370907427 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | VAV1 | GRCh38.p7 | 19:6778230 | GCGTTAAGCCACCAC[A/G]CCCAGACACCACTGT | 7409 |
rs370925497 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6799928 | AGTCTTTGTATGGAC[A/G]TGTGCTTTCATTTCT | 7409 |
rs370969157 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831007 | TGAGGTGGGAGGATC[A/G]CCTGTGGCTAGGAGT | 7409 |
rs370994660 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6812341 | GATTGGAAGCTGATT[A/G]ATATCTGAGGTATTT | 7409 |
rs371038541 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835212 | GTGTATATATATATA[C/T]ATACACACACACACA | 7409 |
rs371038557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781218 | CAGTCCTCGTGTTTT[C/T]ATTTTTCAAATTTTA | 7409 |
rs371072820 | snp | A/C/G | 3.29784e-05 | 0.00406058 | intron-variant | VAV1 | GRCh38.p7 | 19:6829941 | TTTGACGCCGGAACT[A/C/G]TGGGGTCCTCCACGC | 7409 |
rs371088083 | snp | C/T | 1.76089e-05 | 0.00296718 | intron-variant | VAV1 | GRCh38.p7 | 19:6847967 | CAGGCACGGGGACCG[C/T]GCCACCTCTGTCCTT | 7409 |
rs371099055 | in-del | -/ATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776354 | TCCATCCACTCATCT[-/ATCC]ATCCATCCATCCATC | 7409 |
rs371130628 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823684 | TCTGGGTCTCCTCTC[G/T]CTACTTTCTTCCTCA | 7409 |
rs371152886 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773708 | TGCAGGGGCCCAGGC[A/T]GGAGGGGTGGTGGTG | 7409 |
rs371173400 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817891 | CGGGATTTCACCGTG[A/T]TAGCCAGGATGGTCT | 7409 |
rs371195397 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808843 | GGTAGGTAGTCTAGG[A/T]GGGCCTCATTCACAT | 7409 |
rs371209609 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785717 | CAGGCTGGAGTGCAG[C/T]GGCACGATCTCAGCT | 7409 |
rs371213279 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831397 | GCTCACTGCAACCTC[C/T]GCCTCCTGAGTTCAA | 7409 |
rs371217235 | snp | C/T | 0.000181661 | 0.00952876 | intron-variant | VAV1 | GRCh38.p7 | 19:6773022 | CCCAGGTGAGCCCTC[C/T]GCGGGCAGGTGTGCT | 7409 |
rs371261379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6778072 | CTCCTGAGTAGCTGG[A/G]GCTACAGATGCGTGC | 7409 |
rs371286791 | in-del | -/T | 0.5 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6840304 | TCAGAATTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 7409 |
rs371297125 | snp | A/C | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857491 | GACAAAGCCCCCTCA[A/C]CAATCCACAGACAAA | 7409 |
rs371319274 | in-del | -/TATCTATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838295 | TCGTCATCTACATAT[-/TATCTATC]TATCTATCTATCTAT | 7409 |
rs371324167 | snp | A/C | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771887 | AATAACTTAAAAAAT[A/C]AGATTTGTTGGACAA | 7409 |
rs371344768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6795746 | TGGAGTGCAGTGGTG[C/T]GATCTCAGCTCACTG | 7409 |
rs371379432 | snp | A/G | 1.67854e-05 | 0.00289697 | intron-variant | VAV1 | GRCh38.p7 | 19:6836382 | GTGGCAAGATTCAGG[A/G]TTGAAAGTTGACTGC | 7409 |
rs371381376 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775013 | TCAGGTGATCTGACC[A/G]CCTCGGCCTCTCGAA | 7409 |
rs371395033 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835108 | TCTTATTATTACTTA[C/G]TATGTAATTAGCAAT | 7409 |
rs371396842 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814675 | CTTCCTTCCTTCCTT[C/T]CTTTCTTTCTTTCTT | 7409 |
rs371399398 | snp | A/G | 0.175254 | 0.238565 | intron-variant | VAV1 | GRCh38.p7 | 19:6816511 | CTCTCTCTCTCACAC[A/G]CACACAGACACATAC | 7409 |
rs371401110 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6783698 | GTCTCGAACTCCTGA[C/G/T]CTCGGGTGATCCACT | 7409 |
rs371416224 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6839217 | CAGCTGTTTTTTTGT[A/G]TGTGATTTTTTTTTT | 7409 |
rs371433556 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835156 | AGCAAGAGTCAAAAT[G/T]AGAAACAACCCGTGT | 7409 |
rs371451417 | snp | C/G | 0.000555102 | 0.0166506 | intron-variant | VAV1 | GRCh38.p7 | 19:6825272 | TGAGCCCTGGGCTCT[C/G]GTCCCAGCCCTCACC | 7409 |
rs371485881 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | VAV1 | GRCh38.p7 | 19:6825125 | ATCAACATTGAGGTG[A/C]GCCGGCCGATCCCCA | 7409 |
rs371494493 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853731 | GAGAGACTTTATCTC[-/A]AAAAAAAAAAAAAGT | 7409 |
rs371561779 | snp | A/G | 0.000297811 | 0.0121991 | intron-variant | VAV1 | GRCh38.p7 | 19:6822374 | AGGGCGTGGGCGGGG[A/G]GCAGCCCCAGGCCCC | 7409 |
rs371563464 | in-del | -/TCCA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777131 | CCATCCATCCATCCA[-/TCCA]CCCATCCCATCCATC | 7409 |
rs371572261 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6831135 | TGTGGTAGGTGAGGG[C/T]GGGAGGGGGAGCTAT | 7409 |
rs371597441 | snp | C/T | 0.00294325 | 0.0382487 | intron-variant | VAV1 | GRCh38.p7 | 19:6826743 | TTCTCGGGGGCCTCT[C/T]CCGCTCCTCCCCAGG | 7409 |
rs371618173 | snp | C/G | 4.99904e-05 | 0.00499927 | intron-variant | VAV1 | GRCh38.p7 | 19:6854125 | AGGGCTGGGTGACGG[C/G]GAGGGCATGGGGGTT | 7409 |
rs371620071 | snp | G/T | 1.65669e-05 | 0.00287805 | intron-variant | VAV1 | GRCh38.p7 | 19:6828407 | TGACGTCTGACGTCT[G/T]GGTTCTCTCAGGAGC | 7409 |
rs371633811 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783972 | GGAATGCAGGTCTAG[A/G]GCCAGGCATGGTGGC | 7409 |
rs371634138 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6849392 | CTCCCAGGTTCAAGC[A/G]AGTCTTCTGCCTCAG | 7409 |
rs371662587 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850932 | TGGGAATAATAATGA[A/G]TAACAGCAGTTGAAT | 7409 |
rs371698738 | in-del | -/TTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832744 | TCCTCCTCCTTCTTC[-/TTC]CCCTCTTCCTCCTCT | 7409 |
rs371725160 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802041 | GTCCTCATAATGCCT[C/T]TCCTACGTTTGTTTA | 7409 |
rs371741182 | snp | A/G | 1.77391e-05 | 0.00297813 | intron-variant | VAV1 | GRCh38.p7 | 19:6833510 | CTCGCTCTTCTTTAT[A/G]TGTTCCCTGCATCTC | 7409 |
rs371752177 | snp | A/T | 0.000251946 | 0.0112209 | intron-variant | VAV1 | GRCh38.p7 | 19:6836608 | ATGGGGTGGGACCCA[A/T]GTGTAGGGTTATGGA | 7409 |
rs371754541 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784180 | GATCGCTTGAGCCCA[A/G]GAGTTTGATGCTGCA | 7409 |
rs371795670 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | VAV1 | GRCh38.p7 | 19:6810566 | AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCGCCT | 7409 |
rs371815117 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777464 | GCTCTGGAGAAAACA[A/C]AGTGGAACAGGGTAT | 7409 |
rs371850002 | snp | C/G | 3.33433e-05 | 0.00408296 | intron-variant | VAV1 | GRCh38.p7 | 19:6833320 | GTCCTGCATACCGGA[C/G]TTGGTCATCAGTTCC | 7409 |
rs371855851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816841 | TGGTGGCACACTCCT[A/G]TAGTTCCAGCTACTT | 7409 |
rs371861738 | snp | C/T | 2.12114e-05 | 0.00325657 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772772 | GGGTGGTGGAGGCTG[C/T]GAGGGTGCACGGCCG | 7409 |
rs371945414 | snp | C/T | 1.65597e-05 | 0.00287743 | intron-variant | VAV1 | GRCh38.p7 | 19:6821726 | AGCCCCAGTCCTCCC[C/T]CTCCCTGAAGCCCCA | 7409 |
rs372031371 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6828917 | TGGGTGGAGTCAACA[A/T]GGATCTGGGATGGAG | 7409 |
rs372049136 | snp | C/T | 4.95127e-05 | 0.00497533 | intron-variant | VAV1 | GRCh38.p7 | 19:6828587 | AGCCTGGGTCGGCTG[C/T]TGGGGGGCCAGGTTC | 7409 |
rs372054581 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778000 | GGAGTACAGTGGCAT[A/G]ATCTTGGCTCACTGC | 7409 |
rs372082481 | snp | A/C/G/T | 0.000239291 | 0.0109362 | intron-variant | VAV1 | GRCh38.p7 | 19:6852929 | CTTATGGGCTGGCCC[A/C/G/T]CTGGGATAGCATCTG | 7409 |
rs372132249 | in-del | -/TTTATTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838920 | TTATTTATTTATTTA[-/TTTATTT]AGATGGAGTTTCACT | 7409 |
rs372135131 | in-del | -/TGTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830448 | TTTTGTTTGTTTGTT[-/TGTT]GGTTTGTTTTTGAGA | 7409 |
rs372148400 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774514 | ATCTCAGCTCACTGC[A/T]ACCTTAGCCTCTCAG | 7409 |
rs372178005 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834052 | ATATTAACAGCCACA[C/T]TGGGCCGGGTGCAAT | 7409 |
rs372178458 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790825 | GAAATAAAGTGGTAA[C/T]TTCTGAGTTGTCAGG | 7409 |
rs372216771 | in-del | -/ATAG | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6844007 | AAAGCCCTTCGGAAA[-/ATAG]ATAGATTTGATTCTT | 7409 |
rs372254869 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848429 | CTTTTCTTTTTTTTT[C/T]TGACAGAGTCCCTTT | 7409 |
rs372259368 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772467 | GAGTGTCACTGCCGC[C/T]GTCTGCATATGGAGG | 7409 |
rs372268635 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855740 | ATCCATCCATCCATC[C/T]GACCACCATCCACTC | 7409 |
rs372288152 | in-del | -/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856875 | TTTAGGAGGTAATGG[-/GT]GTGTGTGTGTGTGTG | 7409 |
rs372331626 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793495 | ATGGTCTTGGGCGGC[A/G]GCAAGACAGGTACCT | 7409 |
rs372340658 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784875 | TTTCACAGAGATGCT[A/G]GAAATCTCTGTCCCT | 7409 |
rs372380267 | snp | C/T | 0.000148506 | 0.00861575 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828460 | GATGGAGAAGGAGAA[C/T]CTGCGGCTGGCCCTG | 7409 |
rs372411235 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | VAV1 | GRCh38.p7 | 19:6788055 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 7409 |
rs372419531 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787222 | ACTCTGTCACCAAGG[C/T]TGGAGTGCAGTGGTG | 7409 |
rs372443292 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832683 | CTCTTCCTCCTCTTC[A/T]TTCTCTTCCTCCTCC | 7409 |
rs372450721 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827170 | CTCCAGATCTGTCCC[C/T]CTCCCCATCTCCAGC | 7409 |
rs372459204 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6849925 | CTTTCTGGTAGCACA[A/G]TTACTTTTTCCTTTG | 7409 |
rs372497823 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830580 | GAGTAGCTGGGATTA[C/T]GGGCACCCACCACCA | 7409 |
rs372511686 | in-del | -/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798272 | ACAGAGTGAGACTCT[-/GT]CTCAAAAAAAAATAT | 7409 |
rs372524550 | in-del | -/CT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787163 | CATCTCTCTCTCTCT[-/CT]ATTTTTTGTTTGTTT | 7409 |
rs372531316 | in-del | -/AAAG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793343 | ATCTCAAAAAGAAAG[-/AAAG]AAAGAAAGAAAGAAA | 7409 |
rs372560998 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780556 | AAAAGATTGCCTTCT[C/T]CTTTTCTTTCTTTTT | 7409 |
rs372604831 | snp | A/G/T | 0.000134526 | 0.00820051 | intron-variant | VAV1 | GRCh38.p7 | 19:6821902 | GCTCACTGGAGCACC[A/G/T]TCCTGGGGGTGGAGG | 7409 |
rs372629365 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6780051 | GGGAGGCGGAGCTTG[C/T]AGTGAGCCGAGATCA | 7409 |
rs372659664 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794324 | ATAGAAACATTGGGG[-/G]AGAGGAGAATACAGT | 7409 |
rs372670560 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6825679 | GAGGGTTGACTATAC[C/G]GATGCACACAGGGCC | 7409 |
rs372708502 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824542 | CCACATTTTTTTTTT[-/T]CTTTTTTGAGATAGA | 7409 |
rs372762178 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816042 | TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT | 7409 |
rs372781321 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant, missense | VAV1 | GRCh38.p7 | 19:6836997 | TAGGGCAGAAATACA[C/T]CTACTAATGAAATTG | 7409 |
rs372816378 | snp | A/G | 6.60153e-05 | 0.00574485 | intron-variant | VAV1 | GRCh38.p7 | 19:6857030 | TGCAGAGGTTGCACT[A/G]ATGAACTCCTCGTCT | 7409 |
rs372820509 | in-del | -/AATA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798474 | TCATCTCTAATAAAT[-/AATA]AATAAATAAATAAAT | 7409 |
rs372820727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794096 | TACCAATAAACCAAC[A/G]GTAAATGATTTATTT | 7409 |
rs372907021 | snp | A/G | 3.29761e-05 | 0.00406041 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828666 | GCGAGACAACGAGAC[A/G]CTGCGACAGATCACC | 7409 |
rs372944462 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792195 | CACCTCTACAAAAAA[A/C]AAAAAAAGAAGAGAG | 7409 |
rs373014650 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6778873 | TGAGACCCCGTCTCT[A/G]CTTTTTTTTTTTTTT | 7409 |
rs373030484 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834401 | GGCACATGTCACCAC[A/G/T]CTCGGCTAATTTTTG | 7409 |
rs373052003 | snp | C/G/T | 3.39895e-05 | 0.00412235 | intron-variant | VAV1 | GRCh38.p7 | 19:6853095 | GTAGGAGGTCTCAGA[C/G/T]TGGGGGCTTACAGCC | 7409 |
rs373082071 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6829897 | TCGGGATGACTCTTC[A/G]GGAGACCGAGACAAC | 7409 |
rs373113596 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813437 | CATGGCCAGTCTTGG[C/T]TCAATGTGGGAGGGG | 7409 |
rs373136134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6846357 | TTTGAGAGGCTGAGG[C/T]GGGTGGATCACTTGA | 7409 |
rs373192350 | snp | A/C/T | 0.000150536 | 0.0086744 | intron-variant | VAV1 | GRCh38.p7 | 19:6821761 | TACCCAGCCCCCAGG[A/C/T]CCCTGGCTCACACCC | 7409 |
rs373199416 | snp | A/G | 1.66056e-05 | 0.00288141 | missense | VAV1 | GRCh38.p7 | 19:6833195 | CCAGCTCCAACATCT[A/G]TCCGGAGAATGCCAC | 7409 |
rs373202737 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816643 | CAAGCAGCATCCCCA[C/T]ACCGATCTAAGCCTG | 7409 |
rs373230065 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6822721 | TATATATTAAAAAAT[A/G]TATATAAAATATAGG | 7409 |
rs373280918 | snp | A/G | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857789 | ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA | 7409 |
rs373325039 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831388 | ATGATCTCGGCTCAC[G/T]GCAACCTCCGCCTCC | 7409 |
rs373338801 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819165 | CATGAAAACACTTTG[C/T]GATGTGCTGTTTTAT | 7409 |
rs373365529 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6834934 | GTGTCTACAAAAACA[C/T]TTTTAAAAATTAGCG | 7409 |
rs373386756 | in-del | -/AGTC | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6835124 | TATGTAATTAGCAAT[-/AGTC]AGTCAGCTTTCTTAG | 7409 |
rs373395748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791671 | GATACATCTTTAGAG[A/G]GGGCCAGACCCATTC | 7409 |
rs373404205 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847120 | GGTTTCACCATGTTG[C/T]CCAGGCTGGTCTCGA | 7409 |
rs373433509 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6783165 | AGCCTGGTGACAGAG[C/T]GAGACTCCGTCTCAA | 7409 |
rs373449117 | snp | C/T | 1.78646e-05 | 0.00298865 | intron-variant | VAV1 | GRCh38.p7 | 19:6853125 | CTCAGCCCCTTCCCA[C/T]TGTGGAGGGAAACTT | 7409 |
rs373471842 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783537 | TGGAGTGCAATGGCG[C/T]GATCTCTGTTCAGTG | 7409 |
rs373494091 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803337 | GTGGTAACTTCTGGG[G/T]TGTCGGGTCATTGCC | 7409 |
rs373497651 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781035 | TGCCTCAGCCTCCTG[A/G]GCAGCTGGGACTACA | 7409 |
rs373535976 | snp | A/G | 6.70511e-05 | 0.00578974 | intron-variant | VAV1 | GRCh38.p7 | 19:6821871 | TCGAGTGAGTGCTCA[A/G]GCCTGTGGCCGCACA | 7409 |
rs373607221 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816330 | CGGCTACAAAAACAT[G/T]TTTAAAATTAGCTGG | 7409 |
rs373610556 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6833787 | AATGGGCAACAGCGC[A/G]GGGAGGACCCAGGAC | 7409 |
rs373664582 | snp | A/G | 0.000478489 | 0.0154601 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821657 | TCTGTCCTGGACCCC[A/G]ATCGCCCAGAACAGG | 7409 |
rs373685773 | snp | C/G | 1.65704e-05 | 0.00287836 | intron-variant | VAV1 | GRCh38.p7 | 19:6828176 | TCCTTCTCCAGGTGC[C/G]AGGCACATCTCTAGG | 7409 |
rs373692240 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6857101 | AGATTATTCTGAATA[C/T]TGCTGAGCCCTGGTG | 7409 |
rs373710192 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786057 | ATGTTTTATTTTTCT[C/T]CATAGCACTTAGTGC | 7409 |
rs373764318 | snp | A/G | 0.000200864 | 0.0100196 | intron-variant | VAV1 | GRCh38.p7 | 19:6826718 | AAGCTGGAGGTGGGC[A/G]CCGGGCCACTTCTCG | 7409 |
rs373829861 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810702 | AAGAGTGAAACGTTA[C/T]CTCAAAAAAAAAAAA | 7409 |
rs373833790 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836315 | TTCTCCACGTCCTTG[A/T]CAACACTTAGTATTG | 7409 |
rs373852518 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785219 | CTCTATTGCCCAGGC[C/T]GGAGTGCAGTGGTGT | 7409 |
rs373867130 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816604 | ATTGCAGCTCCTCCC[C/T]TAACTTACTCTTGCT | 7409 |
rs373925208 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6832117 | GTTCCTCCTGATCGA[A/G]GACCAAGGTGCCCAG | 7409 |
rs373926059 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787424 | CAAGCAATCTTCCCC[G/T]CCTTGGCCTCCAAAA | 7409 |
rs373948131 | snp | A/G | 1.66846e-05 | 0.00288826 | missense | VAV1 | GRCh38.p7 | 19:6772851 | GGCTCATCCAGTGCC[A/G]GGTGCTGCCGCCCAG | 7409 |
rs373953397 | snp | C/T | 4.95806e-05 | 0.00497874 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6836466 | GTTTCAGGAATACTA[C/T]GGGCTTCCTCCACCC | 7409 |
rs373976688 | snp | C/T | 3.34706e-05 | 0.00409074 | intron-variant | VAV1 | GRCh38.p7 | 19:6821770 | CCCAGGCCCCTGGCT[C/T]ACACCCTCCTGACCC | 7409 |
rs373996111 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856527 | AGGAGTTTGAAACCA[A/G]CCCGGCCAACATGGT | 7409 |
rs373998786 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823194 | GCAATGGCAAGCTCT[C/T]GCTTTACTACAATCT | 7409 |
rs374008787 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6841967 | GCGGTGGTTCACGCC[A/T]GTAATCCCAACACTT | 7409 |
rs374011409 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812676 | CAGAAACAAAGACAA[A/C]CCAAAATACAAAAAT | 7409 |
rs374019545 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795497 | TTATTTATTTATTGA[A/T]TTAATTTTATTTATA | 7409 |
rs374026712 | snp | C/T | 0.000247625 | 0.0111243 | missense | VAV1 | GRCh38.p7 | 19:6828444 | AACACACGCAGGAGG[C/T]GATGGAGAAGGAGAA | 7409 |
rs374052579 | snp | G/T | 0.000437904 | 0.0147905 | intron-variant | VAV1 | GRCh38.p7 | 19:6833788 | ATGGGCAACAGCGCG[G/T]GGAGGACCCAGGACA | 7409 |
rs374076998 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777957 | AGGCGCCTGCCACCA[C/T]GCCTGGCTAATTTCT | 7409 |
rs374113243 | snp | A/G | 0.000336542 | 0.0129676 | intron-variant | VAV1 | GRCh38.p7 | 19:6854138 | GGGGAGGGCATGGGG[A/G]TTGAGCTGGTGGTGG | 7409 |
rs374114757 | in-del | -/CA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831881 | GTGTGTGTGTGTGTG[-/CA]TGTGCACGCCTGCGT | 7409 |
rs374124624 | snp | A/G | 1.69841e-05 | 0.00291407 | missense | VAV1 | GRCh38.p7 | 19:6848024 | CCATGGAGCGGGCAG[A/G]GGCAGAGAGCATCCT | 7409 |
rs374127885 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843401 | ACAATGATGATGACG[A/G]TGATGACAATGATGA | 7409 |
rs374136138 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812808 | TGATTATAATGGTAA[C/T]GATGATGGTGATGGT | 7409 |
rs374139089 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785661 | TTTCTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTT | 7409 |
rs374143798 | snp | A/G/T | 0.000584353 | 0.0170846 | intron-variant | VAV1 | GRCh38.p7 | 19:6833149 | AATAAAATACTGACC[A/G/T]TCTTTTTTTTTTTTT | 7409 |
rs374159927 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6779753 | TGCGGTGGCTCATGC[C/T]TATAATCCTAGCACT | 7409 |
rs374178107 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799060 | GCTTTCCCTGAGCAT[A/G]ATGTCCTGGTTCATC | 7409 |
rs374188276 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801762 | CCCTTCTCCCAGACC[C/G]CAGAGGCCTCTGTCC | 7409 |
rs374241373 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | VAV1 | GRCh38.p7 | 19:6776683 | CCATGTATCCACCCA[C/T]CCACCCACCCACCCA | 7409 |
rs374242028 | snp | A/C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843894 | CTTCTGCTGAATTTT[A/C/G]TAGGCAGGAAGTGTT | 7409 |
rs374290284 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806466 | TGGGTTTTAAGTATG[G/T]CTTCATTCAGTAGCT | 7409 |
rs374292279 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787695 | TCAAACTTCTGGGCT[-/C]AGGAGATTCTCCTAC | 7409 |
rs374333726 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783748 | GCTGGGATTACAGGC[G/T]TGAGCCACCATGCCC | 7409 |
rs374348576 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854700 | GGGTGACAGAACAAG[A/G]CCCTGTCTTTAAAAA | 7409 |
rs374457632 | snp | C/G/T | 6.60791e-05 | 0.0057477 | intron-variant | VAV1 | GRCh38.p7 | 19:6773024 | CAGGTGAGCCCTCCG[C/G/T]GGGCAGGTGTGCTGA | 7409 |
rs374458725 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848692 | ACAGGCGTGAGCCAT[C/T]GTGCCTGGCCTGAAG | 7409 |
rs374535258 | snp | C/T | 3.34722e-05 | 0.00409084 | intron-variant | VAV1 | GRCh38.p7 | 19:6836402 | AAGTTGACTGCCAAC[C/T]ACCCTGTACTCCTGT | 7409 |
rs374598929 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | VAV1 | GRCh38.p7 | 19:6825132 | TTGAGGTGAGCCGGC[C/T]GATCCCCAGCCCTCT | 7409 |
rs374671910 | snp | C/T | 0.00299694 | 0.0385939 | intron-variant | VAV1 | GRCh38.p7 | 19:6826732 | CGCCGGGCCACTTCT[C/T]GGGGGCCTCTCCCGC | 7409 |
rs374675540 | snp | C/G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772638 | CTCCCCCAGCTCCCC[C/G/T]CCGCCCCATGGCTCC | 7409 |
rs374704157 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789519 | GCCTCCCAAAGTGCT[G/T]GGATTTCAGGCATGA | 7409 |
rs374707281 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807414 | GTAGGGTTTGCACTC[C/T]TATGAGGATCTAACG | 7409 |
rs374769222 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853937 | TCTCACTTCTGTTCT[C/T]TCTCCACAGTGGGAA | 7409 |
rs374791697 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816526 | GCACACAGACACATA[C/T]GCACACACAGACACA | 7409 |
rs374809620 | snp | A/G | 0.00159617 | 0.0282053 | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857544 | AAAGCCCCCTCACCA[A/G]TCACAGACAAAGCCC | 7409 |
rs374813140 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793252 | GGCAGGAGAATGGTG[C/T]GAACCTGGGAGGCGG | 7409 |
rs374871785 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846411 | GGCCTACATGGTGAA[A/C]CCCCGCCTCTATTAA | 7409 |
rs374922850 | snp | G/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771681 | CGGGAAGCGGAGCTT[G/T]CAGTGAACTGAGATT | 7409 |
rs374929831 | in-del | -/AAT/ATAAT | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6780112 | AAGACTCTGTCTTAA[-/AAT/ATAAT]AATAATAATAATAAT | 7409 |
rs374937369 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781916 | TTTTAGGAGCTCTTT[A/G]TATATAGGTTGACTT | 7409 |
rs375012890 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855449 | ACAAATCATCCATTC[A/T]TCTGTGCATCCATCC | 7409 |
rs375032773 | snp | A/G | 1.68712e-05 | 0.00290436 | intron-variant | VAV1 | GRCh38.p7 | 19:6836616 | GGACCCAAGTGTAGG[A/G]TTATGGATTCATGTG | 7409 |
rs375037873 | snp | A/C/G/T | 0.000154832 | 0.0087975 | intron-variant | VAV1 | GRCh38.p7 | 19:6852914 | TCCTAGCTCTGCCCC[A/C/G/T]TTATGGGCTGGCCCG | 7409 |
rs375047297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804746 | TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 7409 |
rs375059120 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819733 | TGTGGGAGAGGCCAA[A/G]CCTACAAGCTGTGGG | 7409 |
rs375074399 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837297 | CCTTCCTACATGGGT[A/G]TGGTAGGGAGGAAGG | 7409 |
rs375083543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827987 | GTGGAGAGCTGCTCA[C/T]GTATTTATTCAAATC | 7409 |
rs375093400 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6852610 | CCTGTAGTCCCAGCT[A/T]CTCGGGAGGCTGAGG | 7409 |
rs375134058 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790034 | TACAAAAAAATTAGC[C/T]GGCCATGGTGGCAGG | 7409 |
rs375154187 | snp | C/T | 1.65367e-05 | 0.00287543 | intron-variant | VAV1 | GRCh38.p7 | 19:6833629 | GACATGGGCAAGGTA[C/T]GAGTGGGAGGGAGGC | 7409 |
rs375191897 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6777665 | GCAGTGACTGGCCCA[C/G]CTGGTGGGAATGGTG | 7409 |
rs375191969 | snp | C/T | 0.000124876 | 0.00790079 | intron-variant | VAV1 | GRCh38.p7 | 19:6833497 | TCTGTAAAGGTCACT[C/T]GCTCTTCTTTATGTG | 7409 |
rs375229186 | snp | A/C/T | 0.000987398 | 0.0221977 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821857 | CCTGTCCGACCAGAT[A/C/T]GAGTGAGTGCTCAGG | 7409 |
rs375258065 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770959 | GAGTTTGAGACCAGC[C/T]TGGCCAACATGCTGA | 7409 |
rs375285889 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817893 | GGATTTCACCGTGTT[A/G]GCCAGGATGGTCTCG | 7409 |
rs375367556 | snp | A/G | 8.41928e-05 | 0.00648763 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772773 | GGTGGTGGAGGCTGC[A/G]AGGGTGCACGGCCGG | 7409 |
rs375370523 | snp | C/T | 0.000149453 | 0.00864316 | intron-variant | VAV1 | GRCh38.p7 | 19:6852957 | CTGCCATGTGGTCCG[C/T]CTTCTAGGAGCTGGT | 7409 |
rs375421504 | snp | A/G/T | 3.31279e-05 | 0.00406975 | missense | VAV1 | GRCh38.p7 | 19:6825313 | AGTAGGACCTGCTTC[A/G/T]TGTTCATACTCACTT | 7409 |
rs375425832 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805127 | ATCAGGTAATTGCCA[C/T]GAAAAGCGGTGGTAA | 7409 |
rs375443310 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6828558 | GGCTGATCCTCTAGC[C/T]GGGATTAGGTAGGAG | 7409 |
rs375450474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851817 | ATGTTGCATGCATCT[A/G]TATTTTTTGTCTTAG | 7409 |
rs375465004 | snp | A/G | 6.62987e-05 | 0.00575717 | intron-variant | VAV1 | GRCh38.p7 | 19:6854107 | TGGCCGGGTGAGGCA[A/G]GCAGGGCTGGGTGAC | 7409 |
rs375496500 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817587 | AACTGACATTTTATT[A/T]GGGTGAGATAAACAA | 7409 |
rs375563213 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850361 | CCTTTATATCCTATG[C/G]TTGTCTATATTGGTG | 7409 |
rs375611572 | snp | C/T | 5.03487e-05 | 0.00501715 | intron-variant | VAV1 | GRCh38.p7 | 19:6821881 | GCTCAGGCCTGTGGC[C/T]GCACAGCTCACTGGA | 7409 |
rs375613769 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780292 | CATCATTGTGGGGGA[C/T]AAGTGTATTATTATA | 7409 |
rs375642405 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779928 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 7409 |
rs375644652 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6785300 | CCTCTGCCTCCCAAA[C/G]TGCTCGGATACAGAC | 7409 |
rs375671670 | in-del | GTG/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800792 | ACGCCTGGCAAATTT[GTG/T]TGTGTGTGTGTGTGT | 7409 |
rs375672002 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834107 | TTTGGGAGGCCAAGG[C/T]GGGAGGATCGCTTGA | 7409 |
rs375673506 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849307 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTCACT | 7409 |
rs375676882 | snp | C/T | 6.66978e-05 | 0.00577446 | intron-variant | VAV1 | GRCh38.p7 | 19:6836414 | AACCACCCTGTACTC[C/T]TGTACCCTGTCCTCC | 7409 |
rs375757140 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793343 | CATCTCAAAAAGAAA[-/G]AAAGAAAGAAAGAAA | 7409 |
rs375777917 | snp | A/G | 8.65838e-05 | 0.00657909 | missense | VAV1 | GRCh38.p7 | 19:6826671 | GCAAACACCTGGACC[A/G]TGTGGCCGCAGCCCG | 7409 |
rs375807153 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855535 | CACCCTTCCACTCAC[A/G]CATCTATCTAACCAT | 7409 |
rs375836382 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | VAV1 | GRCh38.p7 | 19:6790001 | TCCAACATGGTGAAA[C/T]CCCATCTCTACTAAA | 7409 |
rs375841727 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805620 | CACACACACATACAC[A/G]CACACACACATGAGT | 7409 |
rs375845100 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780594 | TTTTTTTTTTTGGGA[C/T]GGAGTCTCACTCTAT | 7409 |
rs375853642 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775373 | TCTTAGCTAAAGCTA[C/G]TTTTTGGATGAAGGA | 7409 |
rs375857867 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820565 | TTAATCTTTACCAGA[A/C]GATAATTCAATTTCA | 7409 |
rs375909700 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780112 | CAAGACTCTGTCTTA[A/T]AATAATAATAATAAT | 7409 |
rs375956619 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843063 | TGAATGAATGAATGA[A/G]TGAAGTGCCCTGCCC | 7409 |
rs375959099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6816058 | GGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs375974658 | in-del | -/CTCCTCCTTCTGGTTTCCTTCCTCCTCCTCCTCCTCTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832458 | CCTCTCCTCTTCCTT[lengthTooLong]TCTCCTTCTCCTTTC | 7409 |
rs376025373 | in-del | -/GAA | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771467 | AAGAAAAAAAAAGAA[-/GAA]AGAAGCCTGGCGCGG | 7409 |
rs376029719 | snp | C/G | 6.62065e-05 | 0.00575316 | intron-variant | VAV1 | GRCh38.p7 | 19:6848148 | ACTCATACCCTTTTG[C/G]GGCCTGGGCCCTGCG | 7409 |
rs376113190 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6803665 | TGCTTCCCAGGTCCA[A/G]GCTGTTCTCCTGCCT | 7409 |
rs376115175 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849771 | CATGATCTCATTCTT[C/T]TTTATGGCTGTATAG | 7409 |
rs376128254 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827004 | GCCCTAGCACTGATT[A/G]TACCCCAAGTCGGGC | 7409 |
rs376144873 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790345 | TGCCCTCTTGAGGGA[A/G]GGGGTGGTGTTTTTG | 7409 |
rs376185076 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852703 | TCCAGCCTGGGCGAC[A/G]GAGCCAGACTCCGTC | 7409 |
rs376245956 | in-del | -/G | 0.410149 | 0.19197 | intron-variant | VAV1 | GRCh38.p7 | 19:6796255 | TGAGTGTGTACTCGA[-/G]AGAGAGGTGGGAGAA | 7409 |
rs376279352 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826141 | TCAGGAGTTCGAGAC[C/T]AGCCTGGCCAACATG | 7409 |
rs376290824 | snp | C/T | 3.30017e-05 | 0.00406199 | intron-variant | VAV1 | GRCh38.p7 | 19:6820665 | TCTCCCCTGCCCTTT[C/T]GTACTGCCCCACCCT | 7409 |
rs376316841 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826231 | TAATCCCAGCTACTC[A/G]GGGGGCTGAAGCAGG | 7409 |
rs376350701 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6817956 | CTCCCAAAGTGCTGG[A/G]ATTACAGGCATGAGC | 7409 |
rs376358143 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838093 | CTCATCTGTCTGTCT[A/G]TCTGTCTATCTATCT | 7409 |
rs376389573 | snp | A/G | 0.000153988 | 0.00877328 | missense | VAV1 | GRCh38.p7 | 19:6850740 | ATCACAGAGAAAAAG[A/G]CTTTCCGGGGGCTTA | 7409 |
rs376501253 | snp | C/T | 3.52547e-05 | 0.00419835 | intron-variant | VAV1 | GRCh38.p7 | 19:6847965 | CCCAGGCACGGGGAC[C/T]GTGCCACCTCTGTCC | 7409 |
rs376551116 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826391 | TAAACATTGGGCAGA[A/G]ACAATACCAGGTACT | 7409 |
rs376557105 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803436 | ATGTCTTATGGAAAG[C/G]TGCTTCTGCTCCAGC | 7409 |
rs376573847 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783305 | TGGGTCAATGTCAGG[C/G]GTTGGGGGAGGAGGG | 7409 |
rs376595677 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802216 | AAGTGGGGAGGGATA[A/G]CATTAGGAGATATAC | 7409 |
rs376632201 | snp | A/C/G | 0.000131784 | 0.0081164 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6843152 | CCCTCCTCAGGACCT[A/C/G]TCTGTTCATCTCTGG | 7409 |
rs376664671 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817227 | TAATTTTTTTTGTTT[-/G]TTTTTTTGGTATTTT | 7409 |
rs376668788 | snp | A/G | 1.65018e-05 | 0.00287239 | intron-variant | VAV1 | GRCh38.p7 | 19:6828593 | GGTCGGCTGTTGGGG[A/G]GCCAGGTTCACCCCT | 7409 |
rs376707473 | snp | A/C | 0.000155988 | 0.00883005 | intron-variant | VAV1 | GRCh38.p7 | 19:6822412 | CGGCCTCTCCCCTCG[A/C]TCTCAGCCCAAGATG | 7409 |
rs376727436 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823960 | TGTTTTGTTTTGAAA[G/T]GTGGTCTCACTCTCC | 7409 |
rs376740204 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810994 | GTCCTCATCTGGAAC[A/G]GAGGTACAGACTGTC | 7409 |
rs376743323 | snp | C/T | 0.000379109 | 0.0137627 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772991 | CTGCGTGAGGTCAAC[C/T]TGCGCCCCCAGATGT | 7409 |
rs376762980 | snp | G/T | 0.000742568 | 0.0192544 | intron-variant | VAV1 | GRCh38.p7 | 19:6833643 | ACGAGTGGGAGGGAG[G/T]CTGGGAGGTGAGCTT | 7409 |
rs376862526 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835287 | CATACTTTAAGGTAT[C/G]TAAAAATCAATAAAT | 7409 |
rs376899255 | snp | A/C | 1.66059e-05 | 0.00288144 | intron-variant | VAV1 | GRCh38.p7 | 19:6854114 | GTGAGGCAGGCAGGG[A/C]TGGGTGACGGGGAGG | 7409 |
rs376901761 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6828316 | CAGCCTCCAGGGTCA[G/T]CAGTACGATGGAGGA | 7409 |
rs376942970 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778030 | CAACCTCCTCCTCCC[A/G]GGTTCAAGCGATTCT | 7409 |
rs376975124 | snp | A/G | 5.08858e-05 | 0.00504384 | intron-variant | VAV1 | GRCh38.p7 | 19:6853896 | GTGCCCCCAGAGAGT[A/G]AGTGGGTATCTGCCC | 7409 |
rs376975991 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799873 | AAAAAAAAAGGAAAG[A/G]AAAGAAAACAGAATC | 7409 |
rs377001425 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824897 | CGCTTTTGGGTTATT[A/T]TGAATAATTTCACTG | 7409 |
rs377015913 | snp | A/G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799232 | GAGTGCAGTGGCGCA[A/G/T]TCTCGGCTCACTGCA | 7409 |
rs377031020 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6814385 | GCTCCGGAAGCAACC[A/G]CTGATTTGATTTCTA | 7409 |
rs377063484 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777916 | AGCAATTCTCCTGCA[G/T]CAGCCTCCTGAGTAT | 7409 |
rs377070933 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816334 | TACAAAAACATTTTT[A/C]AAATTAGCTGGATGT | 7409 |
rs377096802 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853463 | GTGCGGTGGCTCATG[C/T]CTGTAACTCCAGCAC | 7409 |
rs377143389 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6844344 | CTGCCTCAGCCTCCC[G/T]AGCTGGGATTACAGG | 7409 |
rs377144898 | snp | A/G | 3.29902e-05 | 0.00406128 | intron-variant | VAV1 | GRCh38.p7 | 19:6828719 | ACCTGGTGAGGCGGT[A/G]GAGCCGGGTGGGCCA | 7409 |
rs377199340 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834590 | TTATTAAATATATAA[C/T]AATTTATTATTTAAT | 7409 |
rs377201160 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | VAV1 | GRCh38.p7 | 19:6816144 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 7409 |
rs377250529 | snp | C/T | 1.64904e-05 | 0.00287139 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6832120 | CCTCCTGATCGAGGA[C/T]CAAGGTGCCCAGGGC | 7409 |
rs377299995 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6830965 | GGCTTGGTGGCACAT[A/G]CCTGTAGCCCTAGCT | 7409 |
rs377302551 | snp | A/G | 0.000148501 | 0.0086156 | intron-variant | VAV1 | GRCh38.p7 | 19:6837088 | GAATAAGGGCAAGGG[A/G]TCCAGGGCGGGTCCT | 7409 |
rs377338056 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836858 | CACACACACACACAC[A/G]CACACACACACACAC | 7409 |
rs377344426 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823059 | AATATACAAGATATA[C/T]GTCCATATGTAGATA | 7409 |
rs377363083 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6819264 | TATGTTTCTGAACCT[A/T]TTGAGCCTTTATAGG | 7409 |
rs377370322 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6834968 | TTCTTGCTTGAGCCC[A/G]GGAGTTCAAGGTTGC | 7409 |
rs377393342 | snp | A/G | 1.64776e-05 | 0.00287028 | missense | VAV1 | GRCh38.p7 | 19:6829911 | CAGGAGACCGAGACA[A/G]CAAGAAGGTGGGGCT | 7409 |
rs377450761 | snp | A/G | 1.64757e-05 | 0.00287012 | intron-variant | VAV1 | GRCh38.p7 | 19:6833673 | TGGTTCTCTTTGGAG[A/G]ATTTCCCGTTCTCAC | 7409 |
rs377474727 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806634 | CGGAGAGTAAATCAC[C/T]GTCCCAGAAGCTGGA | 7409 |
rs377482972 | in-del | -/GT | 0.5 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6831855 | TCTGCAAAGGGGAGT[-/GT]GTGTGTGTGTGTGTG | 7409 |
rs377514352 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789354 | ACCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC | 7409 |
rs377527253 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839769 | CAATCTTGGCCCACC[A/G]CAGCCTCGCCTCCCA | 7409 |
rs377554226 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800525 | ATGTTGGCCAGGCGC[A/G]TCTCAAACTCCTGAC | 7409 |
rs377578938 | snp | A/C | 0.000153988 | 0.00877328 | intron-variant | VAV1 | GRCh38.p7 | 19:6829768 | AGCCAGACAGGAATG[A/C]GTTATCCATCCTTCC | 7409 |
rs377591945 | snp | A/G | 6.66034e-05 | 0.00577038 | utr-variant-3-prime | VAV1 | GRCh38.p7 | 19:6857155 | CCAGGCTCTGAGCCC[A/G]GCGTGGGCAGGCAGC | 7409 |
rs377610258 | snp | A/G | 4.94238e-05 | 0.00497086 | intron-variant | VAV1 | GRCh38.p7 | 19:6833747 | AGGTAAGACTTTCCC[A/G]TGGTCCTTCCTGTGT | 7409 |
rs377642805 | snp | C/G | 6.7297e-05 | 0.00580034 | intron-variant | VAV1 | GRCh38.p7 | 19:6853923 | GCCCCAGACCCTTTT[C/G]TCACTTCTGTTCTCT | 7409 |
rs377691001 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799341 | CCTGGCTAATTTTTT[C/T]GTATTTTTAGTAAAG | 7409 |
rs386806355 | in-del | A/GAAGGAAGGAAGG | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771796 | AGGAAAGAAAGAAAG[A/GAAGGAAGGAAGG]AAGGAAGGAAGGAAG | 7409 |
rs386806356 | in-del | C/GAG | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771970 | GCTGTGATTTGAAAT[C/GAG]GGGATTTAGGAAGAC | 7409 |
rs386806357 | multinucleotide-polymorphism | CG/TA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778937 | GCTGGAGTGCAGTGG[CG/TA]TGATCACAGCTCACT | 7409 |
rs386806358 | multinucleotide-polymorphism | CGTAC/TGTAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783048 | AGCCAGGCGTGGTGG[CGTAC/TGTAT]GCCTGTAGTCCCAGC | 7409 |
rs386806359 | multinucleotide-polymorphism | CA/TG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789714 | GTGATTCTCCTGCCT[CA/TG]GCCTCCAGAGTGGCT | 7409 |
rs386806360 | multinucleotide-polymorphism | CT/TC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792831 | ATCACTACTGGAGGG[CT/TC]TGGTGTGTTATTGAT | 7409 |
rs386806361 | multinucleotide-polymorphism | AG/GA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796255 | TGAGTGTGTACTCGA[AG/GA]GAGAGGTGGGAGAAA | 7409 |
rs386806362 | multinucleotide-polymorphism | AC/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797518 | GACTCAGCCTCACCA[AC/GT]ATAGTAAAACCCAGT | 7409 |
rs386806363 | multinucleotide-polymorphism | AC/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801803 | CTTCCCCGAAGGAGC[AC/GT]GGAAAGCCAGCCGAC | 7409 |
rs386806364 | multinucleotide-polymorphism | AAC/TAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807415 | TAGGGTTTGCACTCC[AAC/TAT]GAGGATCTAACGCTG | 7409 |
rs386806365 | multinucleotide-polymorphism | ACG/GCA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817976 | CAGGCATGAGCCACC[ACG/GCA]CCCAGCCTTAAATTT | 7409 |
rs386806366 | multinucleotide-polymorphism | CC/TA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832606 | TCTTCCTCTTCCTCC[CC/TA]TTCCTCCTCCACCTC | 7409 |
rs386806367 | multinucleotide-polymorphism | CT/GC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832662 | CCCTTCTTCCTCCTC[CT/GC]CCTCCTCTTCCTCCT | 7409 |
rs386806368 | in-del | ATC/CTAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838226 | CTATTATCTATCTAT[ATC/CTAT]ATCATCATCATCATC | 7409 |
rs386806369 | multinucleotide-polymorphism | CTT/GTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840372 | GAGCAGTGGCGCAAT[CTT/GTC]GGCTCACTGCAAGCT | 7409 |
rs386806370 | multinucleotide-polymorphism | AC/CT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854211 | CCATGGAGATCTCTC[AC/CT]GGTGGGAGGGAAGGA | 7409 |
rs397690587 | in-del | -/TCA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838244 | TCATCATCATCATCA[-/TCA]ATCTTTTATCTATTT | 7409 |
rs397713842 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800326 | CTCATTTTTTTTTTT[-/T]TGAGATGGGGTCTTG | 7409 |
rs397726508 | in-del | -/TG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800810 | GTGTGTGTGTGTGTG[-/TG]CAGTCGGGGTTTCAC | 7409 |
rs397734125 | in-del | -/T | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6823142 | TATCTTTTTTTTTTT[-/T]GAGACACGGTTTCTC | 7409 |
rs397759670 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848428 | CTTTTCTTTTTTTTT[-/T]CTGACAGAGTCCCTT | 7409 |
rs397768767 | in-del | -/T | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6800327 | TCATTTTTTTTTTTT[-/T]GAGATGGGGTCTTGC | 7409 |
rs397773448 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833167 | TTTTTTTTTTTTTTT[-/T]AATTTTCCCCTGCCA | 7409 |
rs397822821 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791994 | AGAATGGCTATGGGG[-/G]ATGTGTGTGGAACTT | 7409 |
rs397859558 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780589 | TTTTTTTTTTTTTTT[-/T]GGGACGGAGTCTCAC | 7409 |
rs397859742 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796353 | TATGGGGTGCTTGGG[-/G]TGACAGCCACTTGCT | 7409 |
rs397897629 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6822375 | GGGCGTGGGCGGGGG[-/G]CAGCCCCAGGCCCCC | 7409 |
rs397947288 | in-del | -/TGTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792586 | TGTTTTGTTTTGTTT[-/TGTTT]GTTTTTGTAGAGACA | 7409 |
rs397963649 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839236 | ATTTTTTTTTTTTTT[-/T]AGAGATAGGGTCTCA | 7409 |
rs398033805 | in-del | -/CCAT | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6776180 | CATCCATCCATCCAT[-/CCAT]CCATCCATCCACTCC | 7409 |
rs398033806 | in-del | -/AC | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6836878 | CACACACACACACAC[-/AC]GAGTGATGGGGCAGG | 7409 |
rs398071142 | in-del | -/ACAAAA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778752 | AAAACAAAACAAAAC[-/ACAAAA]CCAATTTTGCCTGGG | 7409 |
rs398101067 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802035 | GGAACCGTCCTCATA[-/A]TGCCTCTCCTACGTT | 7409 |
rs527254788 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789781 | TTTTGTATTTTTTAG[G/T]AGAGAAGGGGTTTTG | 7409 |
rs527259397 | snp | C/T | 8.45945e-05 | 0.00650308 | missense | VAV1 | GRCh38.p7 | 19:6833559 | GGCTACCGCTGCCAT[C/T]GGTGCCGGGCATCTG | 7409 |
rs527309784 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835848 | CTGCAACTTTTGAAG[A/G]ACTTTTTTTTTGTTT | 7409 |
rs527310016 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6833152 | AAAATACTGACCTTC[C/T]TTTTTTTTTTTTTTT | 7409 |
rs527361879 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790077 | CAGCTACTCGAGAGG[C/T]TGAGGCAGAAGAATC | 7409 |
rs527373082 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814455 | TTTTTTTTTTAATTT[A/C/G]TGAGTTATTTTTGCT | 7409 |
rs527433319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839316 | ATAGAACATCCTTCT[A/C]TTTTTTCTTTTAAAA | 7409 |
rs527447069 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6846053 | ATAAAATTATATATT[A/G]TGTATAATTAATATT | 7409 |
rs527459029 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804455 | AGAGTCTTGCTCTGT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs527495754 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804940 | ATGTTAGCCAGGATG[C/G]TCTCGATTGCCTGAC | 7409 |
rs527514878 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771659 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAAGCG | 7409 |
rs527578007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800652 | GTTTTTTTGAGACAT[C/T]CTCGGTCTGTTGCCC | 7409 |
rs527594188 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781781 | CCCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC | 7409 |
rs527610024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805504 | CCCAGGACCTTAGGA[A/G]GCTGAGGCAGGAGGA | 7409 |
rs527693346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806926 | ATAAGAACTTGTTTC[C/T]GCTCTCATGGTGATC | 7409 |
rs527714519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6773327 | CCCAGATGGGACCAA[C/T]CAGAGGTCTCGGGGG | 7409 |
rs527725396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847802 | GTGACCTGTAGAAGT[A/G]GAAGCCCGCTCCCCA | 7409 |
rs527731577 | in-del | -/ATAAA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790197 | ATAAAATAAAATAAA[-/ATAAA]TGCTGGGGAGAGGAA | 7409 |
rs527768484 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795968 | GATTCCAGGGGTGAG[C/T]CACCGCACCCGGCTA | 7409 |
rs527789103 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839499 | TCTCAAACTCCTGAC[C/G]TCAAATGATCTGCCT | 7409 |
rs527798093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834523 | GCTGGGATTACAAGC[A/G]TGAGCCACTGTGCCC | 7409 |
rs527830621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801772 | AGACCCCAGAGGCCT[C/T]TGTCCCTGCACACTG | 7409 |
rs527835052 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778496 | TGGAGAGCCACACCT[G/T]GGTTCAAATTCTGGT | 7409 |
rs527857465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817437 | AATCACCTGAGGAGA[A/G]TGTTAATATGCAGAT | 7409 |
rs527861166 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6853826 | GGGCATCTAATACTC[A/T]GCAGAAAAGAGCACT | 7409 |
rs527866484 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777711 | GATGAATCTCCAAGC[A/G]GCTGGTCCCCTTGAG | 7409 |
rs527894766 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784226 | GCTACCACTGTACTC[C/T]AGACTGGACAAAAGA | 7409 |
rs527920218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778083 | CTGGGGCTACAGATG[C/T]GTGCCACCATGCCTG | 7409 |
rs527969888 | snp | C/T | 6.61824e-05 | 0.00575212 | intron-variant | VAV1 | GRCh38.p7 | 19:6773043 | CAGGTGTGCTGAGGG[C/T]TGGAGACGGGGGTCC | 7409 |
rs527987644 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780588 | CTTTTTTTTTTTTTT[-/TT]GGGACGGAGTCTCAC | 7409 |
rs528017561 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812049 | ATGCTTATGACAAAT[A/G]CTCCTATTCTATTGG | 7409 |
rs528042198 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848774 | TTCCAGGAATTTCTA[A/T]TTTTTTTAATTTAAT | 7409 |
rs528042271 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV1 | GRCh38.p7 | 19:6855846 | ATCTATCTATCTATC[C/T]ATTCATTATCTATCT | 7409 |
rs528053599 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6813401 | ACATCTTGTTTCTTC[C/T]ACCCTGTTCTTTTAG | 7409 |
rs528060585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780089 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTC | 7409 |
rs528069290 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818359 | TTGGAGGCTTAAACA[A/G]CAGAAATTTATCTTC | 7409 |
rs528075746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855430 | TCTATCCATCTATCT[A/G]TCCACAAATCATCCA | 7409 |
rs528081310 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6784090 | AAGGTCCCGTCTCTA[-/C]AAAAAATAAAAAAAT | 7409 |
rs528106816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779917 | GAGATCGAGACCATC[C/T]TGGCTAACACGGTGA | 7409 |
rs528146087 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6808205 | TAATCCCAGCTACTC[A/G]AGAGGCTGAAGGAGG | 7409 |
rs528150572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849391 | CCTCCCAGGTTCAAG[C/T]GAGTCTTCTGCCTCA | 7409 |
rs528232253 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813811 | GTAATCTCAGCACTT[G/T]GAGAGCCTGTGGTGG | 7409 |
rs528241961 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852716 | ACAGAGCCAGACTCC[A/G]TCTCAAAGAAAAAAA | 7409 |
rs528259480 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829367 | AGGGGCGTGGCCAGG[C/T]TCCTAGATGGACAGG | 7409 |
rs528262917 | snp | A/G | 8.63744e-05 | 0.00657113 | intron-variant | VAV1 | GRCh38.p7 | 19:6822359 | GGGTCGGGCCTGGGG[A/G]GGGCGTGGGCGGGGG | 7409 |
rs528297651 | snp | A/C | 1.65012e-05 | 0.00287234 | missense | VAV1 | GRCh38.p7 | 19:6828458 | GCGATGGAGAAGGAG[A/C]ACCTGCGGCTGGCCC | 7409 |
rs528305636 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6828367 | TGGAAGGCCCTCCCC[A/G]CAGGGAGAAGGGGAG | 7409 |
rs528310435 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840590 | AGGCGTGAGCCACTG[C/T]GCCCGGCCTTTTTTT | 7409 |
rs528312787 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796353 | TATGGGGTGCTTGGG[A/G]TGACAGCCACTTGCT | 7409 |
rs528314475 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835000 | GTGAGCCATGATCAC[A/G]CCACTGCACGCCAAC | 7409 |
rs528361145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808373 | ATAATTACCTTAGGA[C/T]AACAGGCATAAGCTT | 7409 |
rs528392862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785762 | CCTCCTGGGCCCAAA[C/T]GATTCTCCTGCCTCA | 7409 |
rs528435442 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6793321 | CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA | 7409 |
rs528467272 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6831525 | CACCACATTGGTCAG[G/T]CTGGTCTCAAACTCC | 7409 |
rs528482441 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792505 | AACAGGTCTTGGGGA[G/T]TTTGATCAAGCAAGG | 7409 |
rs528485265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824526 | TCCATTGTATGGATG[A/G]ACCACATTTTTTTTT | 7409 |
rs528509990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792835 | CTACTGGAGGGCTTG[A/G]TGTGTTATTGATATC | 7409 |
rs528523036 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6831104 | AAAAATAAATGAATG[A/T]AACAGGAGATGTGGC | 7409 |
rs528544238 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV1 | GRCh38.p7 | 19:6814694 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 7409 |
rs528559012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780986 | CGATCTCTGCTCACT[A/G]CAACCTCCACTTCTT | 7409 |
rs528563020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819393 | AAGAAACCAACCCTA[C/T]TGACACCTTGATCTT | 7409 |
rs528564492 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787635 | TAAGTTTTGCTCTGT[C/G]ACACAGGCTGGAGTG | 7409 |
rs528566912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6856404 | ATGAATCAGACGGTG[A/G]TATGTGCTATAGAAA | 7409 |
rs528580825 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818883 | CACTTTGGGAGGCCG[A/C]GGCGGGTGGATCACC | 7409 |
rs528658864 | in-del | -/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772518 | CTAGCTGGCCTGACT[-/C]CCCCAGCCCCCCAAC | 7409 |
rs528669912 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6808004 | CAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAA | 7409 |
rs528729181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6842162 | TGGAACCTGGGAGGC[A/G]GAGGTTGCTGTGAGC | 7409 |
rs528763700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792422 | AGGCAGGGTGGTGTC[C/T]AGGTTTACAGCTTAG | 7409 |
rs528767023 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6797739 | ACAAGAGTGAAACTC[C/T]GTCTAAAAAAAAAAA | 7409 |
rs528795557 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6836879 | ACACACACACACACA[C/G]GAGTGATGGGGCAGG | 7409 |
rs528822603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803552 | TAAGCTGTGGTGCAT[C/T]CAGACAATGGAATAT | 7409 |
rs528822766 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782564 | TATAAGTCAGGGTAC[A/G]TATGTTAACTGCTGT | 7409 |
rs528829813 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854561 | CTACATAAATAAAAA[A/T]AAAAACAAAAACATT | 7409 |
rs528833491 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779289 | ACTCCTGGCCTCAAG[A/C]AATTCCTCCCGCCTT | 7409 |
rs528836603 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785699 | GAGTCTTGCTCTATC[A/G]CCCAGGCTGGAGTGC | 7409 |
rs528944314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773468 | TGTGTCTCCTCCTCC[C/T]GGGCCCTGGGCCCCT | 7409 |
rs528964250 | in-del | -/AAAT | 0.0412342 | 0.137538 | intron-variant | VAV1 | GRCh38.p7 | 19:6782333 | GACTCCATCTAAAAT[-/AAAT]AAATAAATAAATAAA | 7409 |
rs528970495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813307 | CTGATTGAGTGGCCT[C/T]ACAACATGGTCGCCG | 7409 |
rs528971666 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | VAV1 | GRCh38.p7 | 19:6779895 | GGCGGGCGGATCACA[A/G]GGTCAGGAGATCGAG | 7409 |
rs528998117 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856399 | ACATAATGAATCAGA[C/T]GGTGATATGTGCTAT | 7409 |
rs529103127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795388 | CGCGAAATAGGAGCC[C/G]TACTTCATTGCAGGA | 7409 |
rs529141095 | snp | A/G | 0.000307003 | 0.0123858 | intron-variant | VAV1 | GRCh38.p7 | 19:6822334 | TGTCCATGCCGGTGC[A/G]TGACGTGGAGGGTCG | 7409 |
rs529178627 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6828323 | CAGGGTCAGCAGTAC[A/G]ATGGAGGAGCTGGTG | 7409 |
rs529239124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793922 | GCTTCAAGCAGTATC[A/C]ATTAAATGATTGATA | 7409 |
rs529250521 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6797127 | ATCCCAGCTGCTCAG[A/G]AGGCTGAGGCAGGAG | 7409 |
rs529265762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773987 | AGCTCCCATCTGGTC[C/T]TCAGGCTGGCCCTGC | 7409 |
rs529296421 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830378 | TGAGCACCTACTATA[C/T]CCAGGGCACTCTTCT | 7409 |
rs529334133 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836175 | CACCGTGCCCAGCCA[G/T]GACACATGTTTTCAT | 7409 |
rs529384272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792303 | TCCAGCTCACATTTT[C/T]ATTGAGGAGGAAGGG | 7409 |
rs529419685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841716 | CCTGACCTCGTGATC[C/T]GCCTGCCTCGGCCTC | 7409 |
rs529437538 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6853996 | CCGCTATGACTTCTG[C/T]GCCCGAGACCGATCA | 7409 |
rs529451253 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807761 | ACTTTGGGAGGCCAA[A/G]GTGGGCAGATCATGA | 7409 |
rs529471554 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6773846 | ATGTCTGGTTCCCCA[C/G]GGCTGCTGGGTGGGA | 7409 |
rs529504728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848699 | TGAGCCATCGTGCCT[A/G]GCCTGAAGGCTTTTA | 7409 |
rs529507246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796587 | GGCTTCTTGTACTAA[A/C]CTCACTGGCTATTCC | 7409 |
rs529507508 | in-del | -/TCTT | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6832518 | CTCCTTTCCTCCTCC[-/TCTT]TCCTCCTCCTCCCCT | 7409 |
rs529554969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6836126 | TGATCTTCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 7409 |
rs529585985 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802362 | AAAATTAAAAAAAAT[A/G]AAGGACCTCCTGTCC | 7409 |
rs529599782 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783007 | CAATATGGGGAAATC[C/T]GGTTTCTACTAAAAA | 7409 |
rs529607607 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842095 | GCCGGGCGTGGTGAC[A/G]CACACCTGTAATCCC | 7409 |
rs529631660 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6835216 | ATATATATATACATA[C/T]ACACACACACACACA | 7409 |
rs529653230 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784730 | AACTCCTGGCCTCAA[A/G]TGATCTACCCGCCTC | 7409 |
rs529697214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842948 | CCTGCTTTATATGAT[A/G]CTGGGGCAGTCTCTC | 7409 |
rs529745516 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775896 | AGGTGTGCAGGCTGG[A/T]ATGAGAATTCTTCCC | 7409 |
rs529759619 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6798580 | ATCATTTGAACCCAG[G/T]AAGTCGAGGCTGCAG | 7409 |
rs529820527 | in-del | -/AATA | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6798473 | TCATCTCTAATAAAT[-/AATA]AATAAATAAATAAAT | 7409 |
rs529853587 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780897 | ATCATTTATACCATA[C/T]TTTATACAAAGATTT | 7409 |
rs529875285 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818841 | AACAAACTGGCCGGG[C/G]GTGGTGGCTCACACC | 7409 |
rs529890879 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6814996 | TGTTGAGTTGCTACC[A/G]CATCTTTCATGTGTC | 7409 |
rs529914012 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6786520 | GGGTGCAGTGGCTCA[C/T]GCCTGTAATCTTAAG | 7409 |
rs529931517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850049 | CCAATTTACAGTCCA[G/T]CCCACAGTGTAGAGG | 7409 |
rs529940895 | in-del | -/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6843688 | ATCTACTTCATAGTG[-/T]TTTTTAGGAGGCGTA | 7409 |
rs529977254 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | VAV1 | GRCh38.p7 | 19:6814682 | CCTTCCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 7409 |
rs530002364 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6856773 | AAAAAGAAAAGGGGC[A/T]AAGGAGTGTTGGGGT | 7409 |
rs530010415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851765 | ACCCATGGTCTGTGG[A/G]CCCTTGAGAAGCTGA | 7409 |
rs530070134 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823037 | TTTTATATAGATATA[C/T]ATTTTTAATATACAA | 7409 |
rs530093302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815833 | AAAATTGAGAGCATG[A/G]TGGGTGGAAGCTCAT | 7409 |
rs530119218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852474 | CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCCGA | 7409 |
rs530176039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816269 | TCATGATCTGCCCTC[C/T]TCGGCTTCCCAAAAT | 7409 |
rs530210465 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786890 | TATTTTTGGTATTCC[A/G]CATATTCAGAAAAAC | 7409 |
rs530225077 | snp | A/G | 1.74491e-05 | 0.00295368 | intron-variant | VAV1 | GRCh38.p7 | 19:6832233 | TCCCTCTTTCTGTCC[A/G]CAGAGGGGCAGGGGC | 7409 |
rs530225752 | snp | A/C | 1.6768e-05 | 0.00289546 | intron-variant | VAV1 | GRCh38.p7 | 19:6825131 | ATTGAGGTGAGCCGG[A/C]CGATCCCCAGCCCTC | 7409 |
rs530268393 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789107 | GAATCGCCCTGGGGG[C/T]GGGCAAACCAGTTTT | 7409 |
rs530382349 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6820056 | AGGCATGGTGGCTCC[C/T]ACCTGTAATCTCAGC | 7409 |
rs530409430 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6808257 | GCGGAGTTTGCAGTG[A/T]GCCAAGATCACACCA | 7409 |
rs530430545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849509 | GTGGGGGGAAAGTTT[C/T]ACCATGTTGGCCAGG | 7409 |
rs530435791 | in-del | -/A | 0.106278 | 0.204558 | intron-variant | VAV1 | GRCh38.p7 | 19:6797744 | AGTGAAACTCCGTCT[-/A]AAAAAAAAAAAAAAA | 7409 |
rs530456214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793990 | TAAATGACTTCTTTA[C/T]CATTTATGAAAAATT | 7409 |
rs530456526 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787872 | ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT | 7409 |
rs530508309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814628 | TCTTTCTTTCTTTCT[C/T]TTCTTTCTCTCCTTC | 7409 |
rs530663220 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849162 | AGGTATATTGCACAA[C/T]GCTGAGGGTTGGGGC | 7409 |
rs530676223 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808764 | AATATTTGTTATTCC[A/C]ATTAATTTAGTAAAT | 7409 |
rs530706867 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855882 | TCTATCCACCTACCC[A/G]TCAATCCAATAATCC | 7409 |
rs530716309 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847845 | GGCCCCTGCCTCCAC[A/G]GGGCCTACCTTGGTG | 7409 |
rs530766086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6788318 | AAGCCAAGGTCCTAG[C/T]ATTATCCTTCGTTGA | 7409 |
rs530773921 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6787458 | CTGGGATTGCAGGCG[A/T]GAGTCACCGCACCCA | 7409 |
rs530786942 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827852 | TGATCCTCCCGCCTC[A/G]GCCTCCCAAAGTTCC | 7409 |
rs530806061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825594 | TGGGTAGTCACTTAA[C/T]CTCTCTGTGCTTCTG | 7409 |
rs530901352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776098 | TCCATCCATCCATCC[A/G]TCCATCCATCCATCC | 7409 |
rs530926069 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819460 | ATGAATAGAATTGTA[C/G]AATACATGGCATTTT | 7409 |
rs530959929 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6813186 | GTTGCACACAGATGT[C/T]GGCTGGGGCTGCAGT | 7409 |
rs530999582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815723 | TCCCGGCTGTGTGTC[C/T]CACCTCAGTTTCCTT | 7409 |
rs531038452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819905 | AGATACTCAAAAGCT[A/G]GGGCCATGTTACATG | 7409 |
rs531038460 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6815200 | TTGCCTGGGCCGGAG[C/T]GCAGTGGTGCGATCA | 7409 |
rs531048165 | in-del | -/ACC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832618 | TCCTATTCCTCCTCC[-/ACC]TCTTCTTCCTCCTCC | 7409 |
rs531055722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843473 | GTTGTTTTTGTAGGA[C/T]TTTTTGTTTTGTTTG | 7409 |
rs531147026 | snp | C/T | 0.0054002 | 0.0516811 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6836499 | TGGAGCCATTGGACC[C/T]TTTCTACGGCTCAAC | 7409 |
rs531149368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792959 | ACTCAGTGCTAGGCA[C/T]ATGGACTCCAGTTGT | 7409 |
rs531254522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831581 | CCTCCCAAAATGCTG[C/G]GATTACAGGTGTAAG | 7409 |
rs531346505 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794449 | GTTTGAGGCTGCAGT[A/G]AGCTATGATTGCATC | 7409 |
rs531374806 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852443 | GAACCTGTTTTTGGC[C/T]GGGCACGGTGGCTCA | 7409 |
rs531415509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789314 | CTGGAGTGCAGTGGC[A/G]CGATCTCGTCTCACT | 7409 |
rs531422195 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782706 | GCAACATACAAGATC[C/T]CCATCTCTACAAAAT | 7409 |
rs531430628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776783 | TTTATTTATTTACGG[C/T]GTCTCACTCTGTCAC | 7409 |
rs531431175 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778116 | TAATTTCTGTATTTT[C/T]AGTAGAGACAGGGTT | 7409 |
rs531457215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826275 | CCCGGGAGATGGAGG[C/T]TGCACTGAGCCCAGA | 7409 |
rs531518751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810379 | AAAACACTTAGATTC[A/G]TTCCTGGCTTGTAGA | 7409 |
rs531553167 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810723 | AAAAAAAAAATTACT[A/C]TAAGTTGATTCTGAA | 7409 |
rs531563416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847256 | GCCGCCATCACTGCC[A/G]TTTAGCTCCAAAACA | 7409 |
rs531582246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812019 | TTTCTCCTTAAATAC[A/G]GTGCCCTGAAAGTGA | 7409 |
rs531653951 | snp | A/C | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6853653 | GGAGAATCACTTGAA[A/C]CCAGGAGGCATAGGT | 7409 |
rs531676265 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801135 | CCTGTAAGGGCAGAG[A/C]TCTGTTTGTCTTGAT | 7409 |
rs531679122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804758 | AGACGGAGTCTTGCT[C/T]TGTCGCACAGGCTGG | 7409 |
rs531710227 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840280 | GGCTCATCCATGTTG[C/T]GGAATGTGTCAGAAT | 7409 |
rs531717010 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805647 | GAGTTGGGGGGATGG[C/T]TTCAGGATGAATCAA | 7409 |
rs531734406 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6778084 | TGGGGCTACAGATGC[A/G]TGCCACCATGCCTGG | 7409 |
rs531759939 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6806263 | AGCTAATTTTTGTAT[C/T]TTTAGTAGAAACGGG | 7409 |
rs531764040 | in-del | -/ATG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812830 | GTGATGGTGGTGATA[-/ATG]ATGATGATGATGATG | 7409 |
rs531764061 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772547 | ACTCCCCATGCCCAG[G/T]CCTGTGTCGAGTGGG | 7409 |
rs531767405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783618 | CTCCCAAGTAGCTGG[A/G]ATTACAGGCATGCAC | 7409 |
rs531778648 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6846043 | GTTAGGTGACATAAA[-/ATT]ATATATTATGTATAA | 7409 |
rs531785541 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799590 | TATTTCTCCGAATGC[C/T]ATCCCTCTCCTAACC | 7409 |
rs531810783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6821395 | GACAGAGTGAGACTC[C/T]GTTAAAAAAAATACT | 7409 |
rs531852007 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844256 | GCTCCCATCTTCTTG[A/T]TGCCCAGGCTGGAGC | 7409 |
rs531854060 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818115 | GTGCACCACCACACC[C/T]AGCTGACTTTTTATT | 7409 |
rs531858639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811546 | GCTTGGCTGAAGACA[C/T]TGGGGAAGGTTTCCT | 7409 |
rs531892729 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6816793 | ATGGTGAAATCCCCA[A/T]CTCTAGCAAAAAATA | 7409 |
rs531909724 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6803204 | AAGTCCTGCTCCTCG[C/G]AGAGCAGGGCTACCC | 7409 |
rs531917036 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6819510 | GAGCATGTTTTTAAG[A/G/T]TTCATCCATGTTGTA | 7409 |
rs531952777 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797431 | AAAATGGCCGGGCAC[A/G]GTGGCTCATGCCTGT | 7409 |
rs531968562 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801697 | CCGGCTCCCTGGTGC[C/T]GGGGTGGGGGTGGGG | 7409 |
rs531996933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804662 | CCTCAGGTGTTCTGC[C/T]TGCCTTGGCCTCCCA | 7409 |
rs532015722 | snp | C/T | 0.000157498 | 0.00887267 | intron-variant | VAV1 | GRCh38.p7 | 19:6853117 | CTTACAGCCTCAGCC[C/T]CTTCCCATTGTGGAG | 7409 |
rs532131543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839188 | TTACAGGTGTGAGCC[A/G]CTGCACCCAGCCGCA | 7409 |
rs532194096 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844464 | TCAGGTGATCCACTC[C/G]CCTCAGCCTCCCAAA | 7409 |
rs532202154 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6818073 | GATTCTCTCACTTCC[-/A]CCTCCCAACGTGCTG | 7409 |
rs532229031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804192 | TCCAGAGAATGTGAC[A/G]CACGGCAGGCAAGCC | 7409 |
rs532239607 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810378 | CAAAACACTTAGATT[C/T]GTTCCTGGCTTGTAG | 7409 |
rs532255935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832266 | GGAAGGAGGAACGTG[A/G]TCTAGTCCCTACTCT | 7409 |
rs532314027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815143 | CAGTTGCTTCTTCTT[C/T]TATTTATTTATTTAT | 7409 |
rs532314541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776748 | CATCCATCCACTAAT[C/T]TGTCTTTTTTATTTA | 7409 |
rs532315956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6809502 | ATAGGTGCATTTAGC[A/G]TGTGGCAACCACTTC | 7409 |
rs532368390 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852879 | GGGCCTGCTTCATGT[A/G]AGGAGTTGCATATGG | 7409 |
rs532430950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847034 | TTCTCTTGCCTCAGC[C/T]TCCTGAATAGCTGGG | 7409 |
rs532434178 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6843818 | ATGGTTGTTTTTTTT[C/T]TCTTCTTCACATTTG | 7409 |
rs532506937 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772427 | AGGAGGGGGTGAGAA[A/G]TGGGTGAATTCTGGG | 7409 |
rs532519361 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810963 | GCATGCTTTCAACTG[C/T]TGTTCCAAAACCTTT | 7409 |
rs532519535 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6777937 | TCCTGAGTATCTGGG[A/G]TTACAGGCGCCTGCC | 7409 |
rs532540556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811460 | CAGCACAGGCGTCTT[C/T]GTTGTCAGGCCTGGG | 7409 |
rs532542080 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6852497 | GAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG | 7409 |
rs532554639 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6789140 | AGGGAGTGAGCTTGC[G/T]GTCTTGGGGAAAATC | 7409 |
rs532565104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826202 | AATTAGCCAGGCATG[A/G]TGGCAGGTGTCTGTA | 7409 |
rs532588549 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783497 | TTTTTTTTTTGAGAC[A/G]GAGTTTTGCCCTTTT | 7409 |
rs532631342 | snp | C/T | 0.200492 | 0.245049 | intron-variant | VAV1 | GRCh38.p7 | 19:6832593 | CTCCTCGCCCTCCTC[C/T]TCCTCTTCCTCCTAT | 7409 |
rs532633464 | snp | A/G | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6821350 | AGGTTGTAGTGAGCC[A/G]AGATGGTGCCACTGC | 7409 |
rs532756117 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779844 | AGGCCGGGCACGGTG[A/G]CTCACACCTGTAATT | 7409 |
rs532773030 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6788499 | TGCCTCAGCCTCCCT[A/T]GTAGCTGGGATTACA | 7409 |
rs532773909 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856770 | AAGAAAAAGAAAAGG[G/T]GCTAAGGAGTGTTGG | 7409 |
rs532849723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783078 | CCAGCTACTCAGGAG[G/T]CTGAGGCAGGAGAAT | 7409 |
rs532858837 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6785094 | TTTGCACTGGCTCTT[C/T]CTTCTTCAGGGATTT | 7409 |
rs532861266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778627 | GTGGTCCCAGCTACC[C/T]GAGAGGCTAAGTGGG | 7409 |
rs532952247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821933 | GTGTGGGGGGACATG[A/G]CCTTGCCCTCCGGGA | 7409 |
rs533007043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847155 | CTGACCTTGTGATTC[A/G]CCCACCTCGGCCTCC | 7409 |
rs533007189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839800 | GGCTCAGGTGGTCCT[C/T]ACACTTCCGCCTCCC | 7409 |
rs533066916 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810496 | ATCCCCTGAGGTCAG[G/T]AGTTCGAGACCAGCC | 7409 |
rs533082623 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802520 | ATCATGCCCCCTTTC[C/T]CCTCTTTGAGGCATC | 7409 |
rs533128971 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6812690 | ACCCAAAATACAAAA[A/G]TTGATGGGTTGGTGA | 7409 |
rs533133320 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835065 | TAAAAAAATAAATAT[A/G]TGAAATCTATGAATG | 7409 |
rs533145438 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839873 | TTTTTTGTATTTTTC[A/G]TAGCGATGGGGTTTT | 7409 |
rs533179343 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806227 | GAGTAGCTGGGATTA[C/G]AGGTGCATTCCACCA | 7409 |
rs533235045 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6797068 | AAAACCCTGTCTCCA[C/G]TAAAAATACAAAAAT | 7409 |
rs533248236 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791560 | AGGTCCCTGAGACAT[C/T]GCCCCATCTCAAGAT | 7409 |
rs533276383 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6816949 | AGCCTGGGCGACAGA[A/G]CAAGACTCCATCTCA | 7409 |
rs533302630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795129 | GAAATCACGCAGTGT[C/G]ACTTACAGCAGTTTT | 7409 |
rs533309787 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6801056 | CACCCTCTCACCACC[C/G]TCATCATCAATTATT | 7409 |
rs533321326 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777364 | ACACAAAAACCCCTG[C/T]TGTTGAGGAGCCTGC | 7409 |
rs533344647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6812829 | TGGTGATGGTGGTGA[C/T]AATGATGATGATGAT | 7409 |
rs533385633 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | VAV1 | GRCh38.p7 | 19:6779113 | CTGGAGTATAGTGGT[A/G]TGATCACAGCTCACT | 7409 |
rs533407608 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851739 | CTAATGATCTAAGGC[A/G]TATGGTTTTTACCCA | 7409 |
rs533455193 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816002 | GCAACATAATGAAAC[A/T]CTCTGTCTCTACAAA | 7409 |
rs533515059 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6783244 | CCAAATTACATGACT[G/T]CAGTGATAGTGAGAC | 7409 |
rs533535715 | in-del | -/TTTGT | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6827259 | GGGTTTGTTTGTTTG[-/TTTGT]TTTGTTTTGTTTTGT | 7409 |
rs533535838 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855103 | TCCATGAAGGCAGAG[C/T]ACCTTCTTTATTTCA | 7409 |
rs533536965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847919 | AAAGGGGTTCAGGGG[A/G]AAAGGCAACCTCCAT | 7409 |
rs533546002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821017 | GTGTGACCTTGGATA[C/T]GTGGCTGTGCCTCTC | 7409 |
rs533639380 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800927 | CCACCGCACCCAGCC[A/G]CTCACCATCTCTTTG | 7409 |
rs533646793 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6777522 | AGTGGTAAGGTGACA[C/T]TGCAGCAGAGACCTG | 7409 |
rs533651904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6848649 | CTCAAGTGATCCACC[C/T]GCCTCGGCCTCCCAA | 7409 |
rs533658535 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846918 | TTCAGTGGCTTTTTG[-/T]TTTTTTTTTTTTGGA | 7409 |
rs533689024 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6773797 | TGTGGTTGGGTGGGC[A/G]TGTGATGTGGCTGCA | 7409 |
rs533732426 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791866 | GGCAGAGAGGGCAAA[A/G]ACTGTGCAAATGCCC | 7409 |
rs533739812 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6776955 | AGAGATGGGGTTTCA[C/G]CATATTGGCCAGGCT | 7409 |
rs533758688 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6799318 | GACTACAGGTGTGCG[C/T]CACCACGCCTGGCTA | 7409 |
rs533773266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816083 | GGAGTGCAGTGGCGC[A/G]ATCTCGGCTCACTGC | 7409 |
rs533866532 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772123 | CATGTTGGAGGAAGA[A/G]CGAAGAGGCCCGTGT | 7409 |
rs533978253 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813442 | CCAGTCTTGGTTCAA[C/T]GTGGGAGGGGATTAC | 7409 |
rs533979166 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6833402 | AGTCCCTACTTTGAT[C/T]TTCTGCTTCTCCGTC | 7409 |
rs534018388 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831938 | TATTTGGATATCCTA[C/G]AAAGCCCTTTTACAA | 7409 |
rs534212378 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839974 | TGGGATTACAGGCCT[C/G]AGCCGCCATGCCCGG | 7409 |
rs534262602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805763 | GTATATATATATGCA[C/T]ACACACTATATGAAT | 7409 |
rs534335230 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6790004 | AACATGGTGAAACCC[C/T]ATCTCTACTAAAAAT | 7409 |
rs534360479 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772576 | GGCGGAAGAAAGAGA[A/T]GTCAGATTCTGCATG | 7409 |
rs534361456 | snp | A/G | 0.000133125 | 0.00815749 | intron-variant | VAV1 | GRCh38.p7 | 19:6848163 | GGGCCTGGGCCCTGC[A/G]GGCCTGGGAAAAAGG | 7409 |
rs534366209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6846480 | GTAATCCCAGCTACT[C/T]CAGAGGCTGAGGCAG | 7409 |
rs534387569 | in-del | -/T | 0.0209421 | 0.100162 | intron-variant | VAV1 | GRCh38.p7 | 19:6800637 | TTGTTTTGTTTTTTG[-/T]TTTTTTTGAGACATC | 7409 |
rs534389134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796191 | AAACCATAGCAGCGT[G/T]TAAGCACTCCAAGGA | 7409 |
rs534392662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6853192 | AGAGGTCATATCTGT[A/G]CAGTAGCAGGAACCC | 7409 |
rs534415719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845378 | CAACAGAGCGAGACT[C/T]GGTCTCAAAAAATAA | 7409 |
rs534429132 | snp | C/G | 0.0267878 | 0.112589 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771972 | TGTGATTTGAAATGA[C/G]GGGATTTAGGAAGAC | 7409 |
rs534477634 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6821471 | CATTTGAGAGAACGA[C/T]GGTATGGGGAATAGG | 7409 |
rs534510166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817626 | ACAAGAGAAGCAAAA[C/G]TAAGGGGATAGAAAA | 7409 |
rs534519869 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848952 | GTGTGCACCACCACA[C/T]CCAGCTAATGTTTAT | 7409 |
rs534537454 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6822040 | CTTGGGGGACATGGC[A/C]CTGTCCTGGGGTCTT | 7409 |
rs534542585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800366 | CCAGGCTGGAGTGCA[A/G]TGGCATGATCTCGGC | 7409 |
rs534601211 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847592 | TGATGACTAGGTTTT[A/T]TGGCTCTCACTTACA | 7409 |
rs534607753 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6773115 | CTCTGGGCCTGCAAA[A/G]GAGAGGGAATATGCT | 7409 |
rs534630103 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6854156 | GAGCTGGTGGTGGAC[A/G]AGACTGGAACTGGGG | 7409 |
rs534645531 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6773557 | GGCAGGTGGGGGGCT[A/G]CAGCCCCAGGGATCT | 7409 |
rs534653385 | snp | C/T | 0.000230605 | 0.0107354 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6820755 | CTGCTGTGAGAAGTT[C/T]GGCCTCAAGCGGAGC | 7409 |
rs534662662 | snp | G/T | 0.0352966 | 0.128072 | intron-variant | VAV1 | GRCh38.p7 | 19:6780588 | CTTTTTTTTTTTTTT[G/T]TGGGACGGAGTCTCA | 7409 |
rs534671472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774253 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 7409 |
rs534703467 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813633 | ATATTGGCTACTCAT[C/G]GCTGAGGTTTTCTAT | 7409 |
rs534741868 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6818247 | GTCTCACAGAGAAGG[C/T]GTCCTTTGAGGAAAG | 7409 |
rs534742354 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6801978 | CCGCCTCTTCCTGGA[C/G]GAAGGAAGAGGGGCA | 7409 |
rs534913554 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6779475 | TCAGTCTGTAGAGAT[G/T]ATAATTATTCTTTAT | 7409 |
rs534922215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817876 | TGTTTTTAGTAGAGA[C/T]GGGATTTCACCGTGT | 7409 |
rs534946800 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830918 | CATAGGGAGATCCCC[A/G]TCTCTACAAAACATA | 7409 |
rs534962405 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791499 | CGTCTCAAGGTCCTT[C/G]AGATATCTCCTCATT | 7409 |
rs535038652 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773096 | GGCTGACGTGCTGCT[C/T]CACCTCTGGGCCTGC | 7409 |
rs535053660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824098 | GCATGCCACCACACC[C/T]TGCTTAATTCTTTAA | 7409 |
rs535072427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847435 | TGTGCCTGGCTTCTC[C/T]CACTGAGTGTGATGT | 7409 |
rs535090610 | snp | C/T | 1.65307e-05 | 0.0028749 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6854096 | GGGGAGATCTATGGC[C/T]GGGTGAGGCAGGCAG | 7409 |
rs535098859 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772749 | GCAGGGCAGGCGTGC[A/G]GGCGGGTGGGTGGTG | 7409 |
rs535112680 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849654 | GTGTACCCAATGTTT[A/G]ACCCCTGCTTATAAG | 7409 |
rs535117072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774597 | CCACCACCACACCTG[C/G]CTAATTTTTGTATTT | 7409 |
rs535147457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855993 | TTCAGTGACAAATAA[C/T]ACAGACAAAAATCCC | 7409 |
rs535188394 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6829649 | TGGGTGAAGTCAGGA[C/T]GGACAGGTGGGCATG | 7409 |
rs535208524 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807379 | CGCACAAGGTAGATC[C/T]CTCACATGTGGAGTT | 7409 |
rs535267342 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789858 | CCTGCCTTGGCCTCC[C/T]AAAGTGCTGGATTAC | 7409 |
rs535319844 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827045 | CTTCTCACTGAACCC[C/G]AATTCCAACCAACCC | 7409 |
rs535328943 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | VAV1 | GRCh38.p7 | 19:6832571 | CCTCTCCTTCCTCCC[A/C]TTCCTCCTCCTCGCC | 7409 |
rs535422405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783948 | AATGCAGGTATGGAG[C/T]GGGTTTCAGGAATGC | 7409 |
rs535429260 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850133 | TCCTGTGAATTTCCC[G/T]TACTTTTTTTTTTTT | 7409 |
rs535469417 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6817929 | CTGACCTCGTGATCC[A/G]CCCGCCTCGGCCTCC | 7409 |
rs535485294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785371 | GGGTCTCTGTCTATT[A/G]TCCAGGCTGGAGTGC | 7409 |
rs535492965 | snp | A/G | 0.000218031 | 0.0104388 | intron-variant | VAV1 | GRCh38.p7 | 19:6826746 | TCGGGGGCCTCTCCC[A/G]CTCCTCCCCAGGCCC | 7409 |
rs535522169 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6852538 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 7409 |
rs535577352 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831335 | TTTCTTTTTTTGAGA[C/T]GGAGCCTCGCTCTGT | 7409 |
rs535715157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784461 | TAGGAGGGTCAGCAC[C/T]TGGCACCATCCCTTT | 7409 |
rs535715353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791219 | TGAGTTATCTCCTCA[C/T]CTTGAGGTCCTTGAG | 7409 |
rs535724353 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811690 | TTACTGTAAGAATCG[C/G]CAAGAGAAGCTGGAA | 7409 |
rs535739332 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6853376 | CTCTTGGGTTCGAGG[G/T]ATTCTCATGCCTCAG | 7409 |
rs535772485 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796124 | CTCTTAAAGGTCCCG[A/C]TTCTCAACACCATTG | 7409 |
rs535831268 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6823475 | TAAAGATATATATAT[A/G]AAGTATGTATAAGAT | 7409 |
rs535978199 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6824236 | GTGAGCCACCACCCC[A/G]GCCTTAATTTTAGAA | 7409 |
rs535983781 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785922 | TCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 7409 |
rs536012308 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6834666 | ATAATATATAAAATA[A/T]ATATTAATATATATT | 7409 |
rs536016826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808015 | AAAAAAAAAGAAAAG[A/G]AAAAGTTAAAAAAAA | 7409 |
rs536034052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801941 | GATTTGCATATGGGC[A/G]CGATGCCAGCACAGT | 7409 |
rs536094668 | snp | C/T | 0.000132354 | 0.00813385 | intron-variant | VAV1 | GRCh38.p7 | 19:6834004 | GAAAATTCATCTCTA[C/T]TGATGTTGACCCAGG | 7409 |
rs536156848 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813078 | CCCAAACTTAATTGT[A/G]TAAAACAACCATTTA | 7409 |
rs536157677 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819803 | CTGGGGAACCTCAGA[C/G]AGTGCTGAACCTGTT | 7409 |
rs536265992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776308 | CATCCATCCATCCAT[C/T]CATCCATCCATCCAT | 7409 |
rs536293985 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784596 | CCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA | 7409 |
rs536325206 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844805 | CAAGATTTAAGGGGA[C/T]GCTGAAAATCTCAGT | 7409 |
rs536522074 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781970 | AGCTTTGTGGTCTTG[C/G]AGAAAAAAATAATTA | 7409 |
rs536524392 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842254 | CAAATAAATAAATAA[G/T]AAATACATACATAAA | 7409 |
rs536528844 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841215 | CCACCGTGCTGGGCA[A/G]TTTTCTTAATTCTTA | 7409 |
rs536574761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856582 | CAAAAAAATTAGCCG[A/G]GTGTGGTGGCAGGCG | 7409 |
rs536615678 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783897 | CAAAGAAGTCACTGC[C/G]GTAGAACCTCAGGGT | 7409 |
rs536619747 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842186 | TGTGAGCCAAGATCG[C/T]GCCATTGCACTCCAG | 7409 |
rs536625496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809756 | CCACAAAGGTGATCA[C/T]TGCGGTGGCTGCTCT | 7409 |
rs536674096 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785698 | AGAGTCTTGCTCTAT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs536722403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798755 | GACTCAAGCGATCCT[C/T]CTACCCTAGCCTCCT | 7409 |
rs536730077 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6836365 | TTTAGCCATTCTCGT[C/G]GGTGGCAAGATTCAG | 7409 |
rs536732209 | snp | A/C/G | 0.000131928 | 0.00812089 | intron-variant | VAV1 | GRCh38.p7 | 19:6829945 | ACGCCGGAACTATGG[A/C/G]GTCCTCCACGCAGTC | 7409 |
rs536767966 | in-del | -/TATCTATCTATCTATCTATC | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6838296 | TCGTCATCTACATAT[-/TATCTATCTATCTATCTATC]TATCTATCTATCTAT | 7409 |
rs536768607 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6845284 | CAGCTACTCAGGAGG[C/G]TGAGGCAGGGGAATC | 7409 |
rs536851056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6813074 | TATCCCCAAACTTAA[C/T]TGTATAAAACAACCA | 7409 |
rs536860911 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6854742 | AATAAAAGAGATTGT[A/G]GTGGAGAATCACAGG | 7409 |
rs536876270 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824732 | AGACGGGGTTTCACC[A/C]TCTTGGCCAGGCTGG | 7409 |
rs536881263 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6817887 | GAGACGGGATTTCAC[C/T]GTGTTAGCCAGGATG | 7409 |
rs536885204 | in-del | -/TATCTATCTATC | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6838296 | TCGTCATCTACATAT[-/TATCTATCTATC]TATCTATCTATCTAT | 7409 |
rs536889759 | in-del | -/AATAATAATAAT | 0.0524604 | 0.153226 | intron-variant | VAV1 | GRCh38.p7 | 19:6780113 | AAGACTCTGTCTTAA[-/AATAATAATAAT]AATAATAATAATAAT | 7409 |
rs536891075 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823514 | GATACAAATATATAT[A/T]TTATATATATTTTTT | 7409 |
rs536948010 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775738 | GACAAGAAGCCAGAG[A/G]AAGCTGCCACAGGAA | 7409 |
rs536969168 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848342 | GGCTCTTAAAATTAA[C/T]TAATTAATTTGAGTC | 7409 |
rs536993799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6847791 | AAACCTTAGTGGTGA[C/T]CTGTAGAAGTGGAAG | 7409 |
rs537025598 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787658 | CTGGAGTGCAATGGC[A/G]TAGTCATAGCTCCCT | 7409 |
rs537060771 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774721 | ATTACAGGTGTGAGC[C/G]ACTGTGCCCGGCTGC | 7409 |
rs537061106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781163 | CCACCTCGGCCTCCC[A/G]AAGTGCTGGGATGAT | 7409 |
rs537065987 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | VAV1 | GRCh38.p7 | 19:6826199 | AAAAATTAGCCAGGC[A/G]TGGTGGCAGGTGTCT | 7409 |
rs537109761 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797333 | GCCTTTTTACCCCCT[G/T]CACACTCTAAAGTAA | 7409 |
rs537171517 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6803051 | CGGTAGATGAATGCG[A/T]TGTAGGGCAAGGCAA | 7409 |
rs537173149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796770 | ACTTATTTTTTTCTC[A/G]CTTAACACTTACCAC | 7409 |
rs537195633 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6773620 | TAGTAAGGCAGGGCC[C/T]AGTCCTGGGCTCAGA | 7409 |
rs537195940 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | VAV1 | GRCh38.p7 | 19:6779968 | TACAAAAAATTAGCC[A/G]GGCGTGGTTGCGGGC | 7409 |
rs537322836 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807972 | TCCATCCTGGGTGAC[A/C]GAGTGAGACTCTGTC | 7409 |
rs537323237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786778 | ACAGAGACAGGGTCT[A/C]AAAACAAAATGAAAC | 7409 |
rs537341424 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856095 | AGGAGAGGAGTTTGA[C/G]ACCCGCCTGGCCAAC | 7409 |
rs537345272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848826 | TTGGTGACAGTCTGT[C/T]TCTGTTGCCCAGGCT | 7409 |
rs537459674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856479 | GTAATCCCAGCACTC[C/T]GGGAGGCCGAGATGG | 7409 |
rs537476587 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814334 | AACATTTCCATCACT[G/T]GTGGCCTCTCTGAGT | 7409 |
rs537478541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818981 | ATAAGCTGGGTGTGA[C/T]GGCGGGTGCTTGTAA | 7409 |
rs537489629 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832335 | CTTCATTTGGGAAAT[A/G]AGAGGGACAGGCCCA | 7409 |
rs537523686 | snp | A/G/T | 0.00174539 | 0.0294901 | intron-variant | VAV1 | GRCh38.p7 | 19:6843209 | AATGAGAGGTTTCTG[A/G/T]GTTGGGGTTCCAGGC | 7409 |
rs537526753 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803815 | GGTGATCCAGCCACG[C/T]CGGCCTCCCAAAGTG | 7409 |
rs537561929 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6809003 | CAACAGGAGAAGTTG[C/T]AAAGCCTCTATGGGC | 7409 |
rs537572052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6820148 | ACATAGCGAGACCTC[A/G]TCTCTACAAAAAATA | 7409 |
rs537610337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824147 | GGTCTTGCTATGTTG[C/T]CCAGGCTGGTCTCCT | 7409 |
rs537629979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804240 | CTGTGAGGCTTCTTG[A/G]TTTCACCCAAGAAGC | 7409 |
rs537632726 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848666 | CCTCGGCCTCCCAAA[C/G]TGTTGGGATTACAGG | 7409 |
rs537696620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830698 | GCCCATCTTGGCCTC[C/T]CAAAGTGCTGAGATT | 7409 |
rs537711997 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793733 | ATTCCCGGGAGTGGG[G/T]TTAATCAGAAGTCAA | 7409 |
rs537764562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818575 | GTGTCCCCCCAAAAT[C/T]TATACATTGAAGTCT | 7409 |
rs537768364 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854207 | GCTCCCATGGAGATC[C/T]CTCACGGTGGGAGGG | 7409 |
rs537776097 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6798703 | AAAGAAAGAATCAGG[A/G]TCTCCCTATGTTGCC | 7409 |
rs537873988 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775424 | CCCTGGGAGAGCAGC[C/T]GCACTCCAAATACAG | 7409 |
rs537876361 | snp | A/G | 0.000351382 | 0.0132503 | missense | VAV1 | GRCh38.p7 | 19:6825366 | CTGGGCACCCCTGGC[A/G]CAGCCAATCTCTACC | 7409 |
rs537982949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6782186 | AATACAATAATTAGC[C/T]GGGTGTGCTGGTGGG | 7409 |
rs537994067 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837968 | ATCAAAAATTTTTTT[G/T]TTCCTATGGTTTCTC | 7409 |
rs538047483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816461 | CGCTGCACTCCAGCC[C/T]GGACAACAGAGTGAG | 7409 |
rs538081915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837219 | ACTGAGCCCAGAGAG[A/G]GGCCACCCTGGAAAC | 7409 |
rs538081916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843954 | CATTGAACAATTGCT[A/G]GCGCATCAGCTATTT | 7409 |
rs538131334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805135 | ATTGCCATGAAAAGC[A/G]GTGGTAAGGCCGGGC | 7409 |
rs538135673 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845334 | AGGTTGCAGTGAGCC[A/G]AGATTGCGCCATTGC | 7409 |
rs538208343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824830 | CCACCGCACCTGGCC[A/G]GACCACATTTGAAAC | 7409 |
rs538217930 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6806096 | TTGTAAATGAAGCTC[-/T]TTTTTTTTGAGATGG | 7409 |
rs538228224 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839768 | GCAATCTTGGCCCAC[C/T]GCAGCCTCGCCTCCC | 7409 |
rs538232152 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6800235 | AGGAAAACGTACCAA[C/G]TTTTCCAAAGTGGAT | 7409 |
rs538354397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826511 | AAACTGGGACTCAGG[C/T]TTCTTCTCCAGCGGG | 7409 |
rs538367261 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6794700 | AATTTTCACAACAAA[C/T]CCATGGTGTTGGCAC | 7409 |
rs538367398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819111 | ACAAAGTGAGACTCC[A/G]TCCCCCTCAAAAAAA | 7409 |
rs538433318 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810574 | GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAATCGC | 7409 |
rs538441902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852134 | TCCTCCCTCCTCAGC[C/T]TCCTGAATAGCTGAG | 7409 |
rs538454759 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776915 | GGCACCCGCCACCAC[A/G]CCCGGCTAATTTTAT | 7409 |
rs538465557 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788849 | ACTGAGGAACTGTTA[C/G]CTCAGAAGGGTAAAT | 7409 |
rs538488879 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775438 | CTGCACTCCAAATAC[A/G]GTCCTAATCCTCTGT | 7409 |
rs538526993 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771880 | GGAAAAAAATAACTT[A/T]AAAAATCAGATTTGT | 7409 |
rs538542040 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804817 | CAAGCTCTGCCTCCC[A/G]CGTTCACGCCATTCT | 7409 |
rs538588687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797495 | ATCATCTGAGGTTGG[G/T]AGTTCGAGACTCAGC | 7409 |
rs538621727 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818450 | AACTCCAGCCACATG[A/G]GCCTCCTTGCTGTTC | 7409 |
rs538635385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793202 | AGCCAGGCATGGTGG[C/T]GGGTGCCTGTAGTCC | 7409 |
rs538694922 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771450 | GTGAAACTCCGTCTC[A/C]AAAGAAAAAAAAAGA | 7409 |
rs538721560 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6787933 | ATACAAAAAATTAGC[C/T]GGGTGTGGTGACGGG | 7409 |
rs538731183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839412 | GCTGAGATTACAGGC[A/G]TGCACCACCACACCT | 7409 |
rs538785962 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786933 | AATCTATATAAAAAT[C/G]ATCCCTGAAAGTAGA | 7409 |
rs538809686 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827694 | ATCTCTGCCTCCCGG[G/T]TTCAAGCAATTCTCC | 7409 |
rs538842453 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6820110 | GATTCCTCAAGTCCA[A/G]GAATTCAAGACCAGC | 7409 |
rs538846035 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842475 | TGTTCCTACAAAGCA[G/T]AATTCATGGGCACTG | 7409 |
rs538938052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851955 | TTTAACTTCTGAAAA[A/C]TTTCAGACAAGTTAT | 7409 |
rs538942107 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6844020 | AAAATAGATTTGATT[C/G]TTACTCTCTGCCCCC | 7409 |
rs538961613 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6776899 | AGTAGCTGGGACTAC[A/G]GGCACCCGCCACCAC | 7409 |
rs538993805 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838786 | CTAGGCTGGAGTGCA[A/G]TGGTGTGATTTAACT | 7409 |
rs539002682 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798348 | CAGAAACGGTCTTGG[C/T]AGGGCATGGTGCCTG | 7409 |
rs539007200 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778137 | AGACAGGGTTTCAGC[A/T]TGTTGGCCAGGCTGG | 7409 |
rs539010049 | in-del | -/AAAG | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6793335 | GAGACTCCATCTCAA[-/AAAG]AAAGAAAGAAAGAAA | 7409 |
rs539017091 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804784 | GCTGGAGTGCAGTGG[C/T]GCAATCTTGGCTCAC | 7409 |
rs539064207 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799974 | GGTAATGGAATATAT[C/T]GTATGATAGGTGCAT | 7409 |
rs539068477 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6783806 | CTTGGTCACATGGCT[A/C]CATTTAACTACGAGG | 7409 |
rs539091415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794126 | TACCAATAAATCAAC[A/G]GTAAATGATTTATTT | 7409 |
rs539184369 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6776484 | CATCCATCCATTCAT[A/C]CATTCATCCATCCAC | 7409 |
rs539238138 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VAV1 | GRCh38.p7 | 19:6857319 | GTCCCCTCAAGCAGA[C/T]GGGGCTCAAGGGGGT | 7409 |
rs539261873 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794555 | GGGTGTGGTGTCAAG[A/C]GACCAATGCCGTTGA | 7409 |
rs539299731 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6832824 | ACAACAAAAATCTAA[A/C]AATTTCGAAGTGTAT | 7409 |
rs539308981 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804461 | TTGCTCTGTCGCCCA[G/T]GCTGGAGTGCAGTAG | 7409 |
rs539318629 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770915 | CCAGCACTTTGGAAG[A/T]CCAAGGCGGGCAGAT | 7409 |
rs539352210 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775358 | CCATTCTTGTGTATG[C/T]CTTAGCTAAAGCTAG | 7409 |
rs539395084 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849605 | GGCGTGAGCCACTGT[G/T]CCTGGCCAATATTAT | 7409 |
rs539409401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822091 | GGAGCTTGGAGGGAC[A/G]TGGCCTGCCCTTGGA | 7409 |
rs539422753 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830631 | TTTTAGTAGAGACGA[C/G]GTTTCACCATGTTGG | 7409 |
rs539480382 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6815195 | TTGTGTTGCCTGGGC[C/T]GGAGTGCAGTGGTGC | 7409 |
rs539492415 | in-del | -/T | 0.268452 | 0.249318 | intron-variant | VAV1 | GRCh38.p7 | 19:6774922 | ACCATGCCTGCCTAA[-/T]TTTTTTTTTTTTTTT | 7409 |
rs539569513 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6822499 | GTACACTGACACGCT[A/G]GGCTCCATCCAGCAG | 7409 |
rs539606188 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6826450 | GATAATGCTACAATA[A/G]CCTCACATGGGAGAT | 7409 |
rs539689053 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6825974 | CTTGAACCCGGGAGG[C/T]GGAGGTTGCAGTGAG | 7409 |
rs539745319 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6826796 | ACTGAGTTGCAGATG[G/T]TCCACTTTCTGCTGC | 7409 |
rs539865975 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834630 | ATATTAATTAATATA[A/G]TATAGTAATAATATA | 7409 |
rs539867518 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6776736 | TATCCATGGATCCAT[C/G]CATCCACTAATCTGT | 7409 |
rs539900156 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785317 | GCTCGGATACAGACA[C/G/T]GAGCCACTTCACCTT | 7409 |
rs539908625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804829 | CCCACGTTCACGCCA[C/T]TCTCCTGCTTCAGCC | 7409 |
rs539927958 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834008 | ATTCATCTCTATTGA[C/T]GTTGACCCAGGGACA | 7409 |
rs539944688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804613 | GTAGAGATGAGGTTT[C/T]GCCATGTTGGCCAGG | 7409 |
rs539946368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810652 | GGAGGTTGCAGTGAG[A/C]TGAGATCACGTCATT | 7409 |
rs539951543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6844953 | AGTAAGAGGAGGTGG[A/G]TGAGGTGAGTCGGGC | 7409 |
rs539981067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784660 | CACCACACCTAGCTG[A/G]TTTTTGTATTTTTAG | 7409 |
rs540007286 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6806416 | GAAAATAATTTTTTC[A/T]CAATGCCGTTTTGGA | 7409 |
rs540009982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840445 | CGAGTAGCTGGGACT[A/G]CAGGCACTTGCCACC | 7409 |
rs540046583 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847344 | CCCCGGGAACCAAGG[G/T]TCTCCTTCCTGTCTC | 7409 |
rs540059875 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773064 | ACGGGGGTCCTCCCC[A/G]GGGCTGACAGTCGAG | 7409 |
rs540074087 | in-del | -/CTTTCTTTCTTT/CTTTCTTTCTTTCTTT/TTTCTTTCTTTCTTT | 0.25634 | 0.24992 | intron-variant | VAV1 | GRCh38.p7 | 19:6814671 | TTCCTTCCTTCCTTC[lengthTooLong]CTTTCTTTCTTTCTT | 7409 |
rs540112993 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6817853 | ACCTTGCCTGGCTAA[-/T]TTTTTTGTGTTTTTA | 7409 |
rs540117033 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831604 | GGTGTAAGCCACCGC[A/G]CCCGGCTGGCTTCTC | 7409 |
rs540192819 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771179 | AAAAAAAGCCGGGCG[C/T]GGTGGCTCACGCCTG | 7409 |
rs540221536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6821273 | GGGTGTGGTGGCCGG[C/T]GCCTGTAGTCCCAGC | 7409 |
rs540278083 | snp | C/T | 9.53334e-05 | 0.00690345 | intron-variant | VAV1 | GRCh38.p7 | 19:6826562 | ACGCCAGCCTCTGCC[C/T]GACCTTGATGCCAGT | 7409 |
rs540281174 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799136 | CCCCAGTTTGTTTAT[A/C]CATTCATCCCTTGAT | 7409 |
rs540320314 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6838393 | TCAATCAGTTCTTCT[A/G]TCCATCCATCCATCC | 7409 |
rs540358521 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6777914 | CAAGCAATTCTCCTG[C/T]AGCAGCCTCCTGAGT | 7409 |
rs540381986 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825461 | CTGTCTTGCCTAGGC[G/T]GGGCATCTGAGAGAC | 7409 |
rs540394718 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776674 | CTTTTCCATCCATGT[A/G]TCCACCCATCCACCC | 7409 |
rs540400679 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV1 | GRCh38.p7 | 19:6832581 | CTCCCCTTCCTCCTC[C/T]TCGCCCTCCTCTTCC | 7409 |
rs540457311 | in-del | -/AAAATC | 0.0146672 | 0.084371 | intron-variant | VAV1 | GRCh38.p7 | 19:6844856 | AATGCAACATTAAAA[-/AAAATC]AAAATCAAAAACAAG | 7409 |
rs540465832 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799580 | CTACATTAGGTATTT[A/C]TCCGAATGCTATCCC | 7409 |
rs540482262 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839059 | AGGCGCCTGCCACCA[A/C]ATCTGGCTAATTTTT | 7409 |
rs540511558 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826156 | CAGCCTGGCCAACAT[A/G]GCAAAACCCCGTCTC | 7409 |
rs540536988 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815005 | GCTACCGCATCTTTC[A/G]TGTGTCTTCTGTTGC | 7409 |
rs540639386 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6789554 | CCGCACCCGGCTCTT[C/T]CCTTTCTTTTCTGTT | 7409 |
rs540644826 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818843 | CAAACTGGCCGGGCG[C/T]GGTGGCTCACACCTG | 7409 |
rs540663883 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801412 | CGGTGCTGAAAAGTG[G/T]AGTGTGTGCTGGGGT | 7409 |
rs540664950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795364 | CTTCTCTGAACTCTG[C/T]GTATCGCTCGCGAAA | 7409 |
rs540668617 | snp | A/T | 3.29625e-05 | 0.00405958 | intron-variant | VAV1 | GRCh38.p7 | 19:6820691 | ACCCTCATTTCTCTG[A/T]CTCCTCACAGTTCCT | 7409 |
rs540760600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790145 | ATCGTGCAAGTGCAC[C/T]CCAGCCTGGGTGAGA | 7409 |
rs540842341 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | VAV1 | GRCh38.p7 | 19:6853576 | TAAAAAAAAAAAACA[A/T]AAAAATCAGCCGGGC | 7409 |
rs540848477 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6846059 | TTATATATTATGTAT[A/G]ATTAATATTTATTAT | 7409 |
rs540873430 | in-del | -/TTGT | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6795676 | GTCCACTCTTTTTGC[-/TTGT]TTGTTTGTTTGTTTG | 7409 |
rs540892354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794795 | AAAAACATGATTTTT[G/T]ATTCTCACAGATTCT | 7409 |
rs540925441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801036 | GCTCTCTGTGCTTCC[C/T]GGCACACCCTCTCAC | 7409 |
rs540926814 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818796 | TGAGCCCTTAGAGGA[A/G]CCTACAAATATCTAG | 7409 |
rs540950024 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771525 | TTTGGGAGGCTGAGG[C/T]GGGCGGATCATGAGA | 7409 |
rs541002259 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827550 | AAGAGCTAGGATTAC[A/T]GGCCTGAGCAATCGT | 7409 |
rs541016926 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801390 | CAGATCTGCCTGACC[C/G]TCCCACCGGTGCTGA | 7409 |
rs541083328 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802819 | GATGGGCAGTATCCC[C/G]TCTCTGAGCCTCAGT | 7409 |
rs541114512 | snp | C/G/T | 3.30453e-05 | 0.00406467 | intron-variant | VAV1 | GRCh38.p7 | 19:6828040 | GGCTGTTTCTGGGAC[C/G/T]TGCCTCAGTTTCCCC | 7409 |
rs541121177 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812088 | AGTCACATGACTGCA[G/T]CCACATGCAAGGAGA | 7409 |
rs541144952 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6802167 | GGCACAGGAAGGGGA[A/C]CATCACACACAGGGG | 7409 |
rs541152133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795772 | CACTGCAACCTCCGC[C/T]TCCTGGGTTCAAGTG | 7409 |
rs541178506 | snp | C/T | 5.63142e-05 | 0.00530603 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772800 | CCGGCCCTGGGCAGG[C/T]GGTAGCCATGGAGCT | 7409 |
rs541219178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811896 | CCAGGTCGGGGGGCT[C/T]TTCCCCGCAGATAAT | 7409 |
rs541222205 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6817750 | GGAGTGCAGTGGCAC[C/T]GTCGTGGCTCACCGC | 7409 |
rs541233788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784952 | AAGACAAAATCCTCA[C/T]TGTAGCCCACAAGGG | 7409 |
rs541248828 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6817111 | TGGAGTGCAGTGGGG[A/G]TATCTCAGCTCACTG | 7409 |
rs541259976 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811381 | CACTATTGCATGCCA[A/C]CATGTGGTGTTCAGG | 7409 |
rs541268806 | in-del | -/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771066 | TGAGGTCAGGGAAAA[-/C]CTGGGAGGCAGAGCT | 7409 |
rs541347176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773337 | ACCAACCAGAGGTCT[C/T]GGGGGAGCTCCCCAG | 7409 |
rs541369976 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6783017 | AAATCCGGTTTCTAC[C/T]AAAAATACATAAATT | 7409 |
rs541439751 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6773771 | GAAATATATTCAAAT[A/C]CCTATTTGAATGTGG | 7409 |
rs541460411 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6800565 | TCAACCCACCTCAGC[A/G]TCCCAAAGTGCTGGG | 7409 |
rs541534674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842004 | GCCGAGGCGGGTGGA[C/T]CACCTGAGCTCGGGA | 7409 |
rs541562295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794948 | CTGGGATGACTTGAG[A/G]CTATGCTCAGTTGGG | 7409 |
rs541567348 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849166 | ATATTGCACAATGCT[A/G]AGGGTTGGGGCCATG | 7409 |
rs541596109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822797 | AATACAAAATCAAAA[A/G]TATATAAATATATTA | 7409 |
rs541616488 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805464 | CAAAGAAAATAGACC[A/C]GTTGTGGTGGCTCAC | 7409 |
rs541628699 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777082 | ATCTATCATCCACCT[G/T]CCCACCCACCCATCC | 7409 |
rs541699774 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772102 | GGCAGGGCCGTATGT[C/T]CCTGGCATGTTGGAG | 7409 |
rs541723672 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805403 | GCACTCTAGCCTGGG[A/C]CACAGAGCAAGACTC | 7409 |
rs541747775 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6790174 | GAGAGTGAGACTCTG[A/T]CTCAAAAATAAAATA | 7409 |
rs541788717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854315 | ATTGTGCTGGGTGTC[A/G]AGGAGACAGAAACAA | 7409 |
rs541795256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6852749 | AAAGAAAGAAAGAAC[C/T]TGTTTTAGGCAGTGT | 7409 |
rs541809239 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6833108 | GGTCTGTTCATACCA[C/T]GGAATAGTATTCAGC | 7409 |
rs541811371 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840113 | CTGAACCCATTAAAC[A/G]GCAACCACCTATTCC | 7409 |
rs541818210 | snp | A/T | | | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825362 | AGCCCTGGGCACCCC[A/T]GGCGCAGCCAATCTC | 7409 |
rs541818259 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851999 | TGAGTATCTATGAAC[C/G]TTTCATATAGGTTTA | 7409 |
rs541879624 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6827604 | TTTGTTTGTTTGTTT[G/T]TCTTTGTTTTTTGAG | 7409 |
rs541946598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840934 | AGGCATGCACCACCA[C/T]ACCAAGCTAATTTTT | 7409 |
rs541983463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847767 | GCCATCCCCCCGAAT[C/T]CATGTGTCAAACCTT | 7409 |
rs542009108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783370 | CCATCATCTCATGGT[C/T]TTAGCTTCCCGAAGG | 7409 |
rs542032380 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6834913 | TGGGCAACAGAACGA[A/G]ACCCTGTGTCTACAA | 7409 |
rs542033689 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6821237 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAAAT | 7409 |
rs542038713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790196 | AATAAAATAAAATAA[A/G]ATAAATGCTGGGGAG | 7409 |
rs542072654 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | VAV1 | GRCh38.p7 | 19:6816169 | GGACTACAGGCGCAC[A/G]CCACCACGCCCAGCT | 7409 |
rs542143263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778401 | GATGATGTTAAGTTC[C/T]CCAGCCCCAGTGAAT | 7409 |
rs542148307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811302 | CGGCCTCCCATAGTG[C/T]TGGGATTATAAGCAT | 7409 |
rs542254800 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6830090 | TTTAAGATGGAGTCT[C/T]GCTCTGTCGCCAGGC | 7409 |
rs542277241 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838524 | GTCTATGTATTATCT[A/G]TCATCTATCTATTCA | 7409 |
rs542297967 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848439 | TTTTTCTGACAGAGT[C/T]CCTTTGTCGCCCAGG | 7409 |
rs542301423 | in-del | -/TTTT | 0.000838223 | 0.020455 | intron-variant | VAV1 | GRCh38.p7 | 19:6823919 | TTTGTTTTGTTTTGG[-/TTTT]TTTTGTTTCTTTTTT | 7409 |
rs542315135 | in-del | -/T/TT | 0.491885 | 0.0631791 | intron-variant | VAV1 | GRCh38.p7 | 19:6841478 | ACTATTTTTCTTTTC[-/T/TT]TTTTTTTTTTTTTTT | 7409 |
rs542321895 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773720 | GGCTGGAGGGGTGGT[A/G]GTGGATTTGACTGTG | 7409 |
rs542359599 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6828011 | TCAAATCTATCTGCA[C/T]CCACCCTGCAACTGG | 7409 |
rs542379242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834987 | GTTCAAGGTTGCAGT[A/G]AGCCATGATCACGCC | 7409 |
rs542384870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773290 | CTCTCAAGCCCCAGG[C/T]GCCTCTACTGTGGTT | 7409 |
rs542396100 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809709 | GAGGAGTACAAAACG[A/G]ATCAGGAAGACCACT | 7409 |
rs542489991 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829099 | CAGAGCCAGGCTTCT[A/G]GATAGGCAGATGGGT | 7409 |
rs542494394 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784746 | TGATCTACCCGCCTC[A/G]GCCTCCCAAAGTGCT | 7409 |
rs542502495 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842495 | CATGGGCACTGACAG[A/G]TGAATTTCATATGAT | 7409 |
rs542520973 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810218 | TGGTGGTGCATGCCC[A/G]TAGTCCCAGCTGCTC | 7409 |
rs542529795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796896 | GGTTCATAGCTGTAT[C/T]TCCAGCACCTAGACC | 7409 |
rs542564047 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6823858 | GGTTTTTGGCACACA[A/C]AAGATTATGCAGTCA | 7409 |
rs542594700 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6780123 | TTAAAATAATAATAA[-/T]TAATAATAATAATAA | 7409 |
rs542657317 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791940 | GAGTGAGTGGAGGGA[A/G]AGTGGTAAAGAATGA | 7409 |
rs542667315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843267 | TTAGTTATGCATTCT[A/G]TGATCCCTGAGCACC | 7409 |
rs542690958 | snp | A/C | 0.414741 | 0.188044 | intron-variant | VAV1 | GRCh38.p7 | 19:6780065 | GCAGTGAGCCGAGAT[A/C]AGGCCACTGCACTCC | 7409 |
rs542725681 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6818339 | CACAACAAAGTACCA[C/T]GAGCTTGGAGGCTTA | 7409 |
rs542729925 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815310 | TCACACCAGGCTAAT[G/T]TTTGTATTTTTTGCA | 7409 |
rs542809494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841464 | TTGAGGAACCACCAT[A/G]CTATTTTTCTTTTCT | 7409 |
rs542946756 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809097 | TTTTTTTTTTTTTTT[-/TT]GAGATAGGGTCTTGT | 7409 |
rs542975899 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6821522 | TAGGCTTCCAAGAGG[C/T]ATGGGATCTAGCGCC | 7409 |
rs543004222 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6793900 | AATAATTGTAAAGTC[A/G]TAAAGTGCTTCAAGC | 7409 |
rs543009613 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815795 | TTGCTGGGAGGAGTC[C/G]ATGTTATCTCTGCAG | 7409 |
rs543016980 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6831062 | GCACTACAGCTAGGA[C/T]CACAGAGTGAGATCC | 7409 |
rs543020041 | snp | C/T | 0.215144 | 0.247558 | intron-variant | VAV1 | GRCh38.p7 | 19:6836873 | ACACACACACACACA[C/T]ACACACGAGTGATGG | 7409 |
rs543092434 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6828272 | TGGGTCTCTAGGACG[A/C]TCGGGGATGGGTCAC | 7409 |
rs543107256 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811613 | AGTAGGAGTTCACCA[-/G]GCAAATAGGAGAGGA | 7409 |
rs543120941 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6831478 | CACCACGCCCAGCTA[A/G]TTTTTTTGTATTTTT | 7409 |
rs543180855 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780719 | TGGGATTACAGGCAC[A/G]TGCCACCACATCCGG | 7409 |
rs543217757 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6840245 | TGTCTAGCTTGTTTC[A/G]CTTGGCATAATGTAT | 7409 |
rs543218141 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847736 | TCCAGACACCCAGCC[A/C]GACCCAAAGGGCTGA | 7409 |
rs543235465 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800842 | ATGTTGCCCAGGCTG[A/G]TCTTGAACCCCTGAC | 7409 |
rs543236806 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814440 | TGTAGGATTTCACAA[A/T]TTTTTTTTTAATTTG | 7409 |
rs543241120 | in-del | -/GAG | 0.0154538 | 0.0865337 | intron-variant | VAV1 | GRCh38.p7 | 19:6844118 | TGCAAATGAGGCTGA[-/GAG]GAGAGGGTAAGTGAA | 7409 |
rs543272511 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803481 | TCCTCAATTTGGTCC[A/G]TTGTCTGAGCCCCAC | 7409 |
rs543288616 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6806243 | AGGTGCATTCCACCA[C/T]GCCCAGCTAATTTTT | 7409 |
rs543302540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6846664 | ATGTTATACCATATA[C/T]TATACATTTACATAG | 7409 |
rs543330478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6801545 | GGTGCACAGCACACC[C/T]GCCCTCTCTGGGAAC | 7409 |
rs543347533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808639 | CACTTGCCAGCCAGA[C/T]AAAGGGGCTAGAATG | 7409 |
rs543434582 | in-del | -/ATT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788386 | ATTATTATTATTATT[-/ATT]TTGAGACTGAGTCTT | 7409 |
rs543462643 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6797563 | GCAAAATTAGCTGGG[C/G]GTGGTGACGCATGCC | 7409 |
rs543500100 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838800 | AATGGTGTGATTTAA[C/T]TCACTGCAGCCTTGA | 7409 |
rs543503429 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781255 | TTTATTTTGTCAACC[A/G]AAGTGCTAGCCAATC | 7409 |
rs543530723 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6791410 | AGCTAGCTCCTCATC[C/T]CGAGGTCCTTGAGCT | 7409 |
rs543543002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775080 | CCTTCTGTTTCTTTA[A/G]TGCCAGGGGATTACA | 7409 |
rs543558208 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6822899 | TAAAATATAAACATG[A/G]TATATGATATTTATA | 7409 |
rs543566053 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803283 | CACTTTAATTATATG[A/C]AAATTAAAGGGCAGA | 7409 |
rs543571876 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847006 | GCAACCTCCGCCTAC[C/T]GAGTTCAAGCGATTC | 7409 |
rs543588185 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782836 | GCAGTGAGCTATAGA[A/T]CGCGCCGCTGCAGTC | 7409 |
rs543615860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779877 | AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA | 7409 |
rs543618533 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773220 | CCCTGTGTGGGTTCA[A/C]GGGCCCTGAGTTGGC | 7409 |
rs543643237 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813225 | GGCCTTAGCTGGAGG[A/G]TCTACTTCCTGAGTG | 7409 |
rs543661311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786037 | CCAACTTCCCATTCT[C/T]TTTCATGTTTTATTT | 7409 |
rs543677802 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855135 | CCACTGATGACTTCT[C/T]AGCCTCTAGAATTCT | 7409 |
rs543684949 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6774284 | AGGCGCCCGCCACCA[C/T]GCCTGGCTAATTTTT | 7409 |
rs543704998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6823583 | AGCAATCCTCCTGTA[A/T]TCCAAGCCCTTTGTG | 7409 |
rs543749344 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773817 | ATGTGGCTGCATTAT[A/G]TTGCTGTAGCATCAT | 7409 |
rs543805311 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842673 | ATCTTGACAAAATTT[A/T]AAAAAATTAAAAATT | 7409 |
rs543836679 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808078 | AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATTG | 7409 |
rs543841451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842082 | AAATACAAAATTAGC[C/T]GGGCGTGGTGACACA | 7409 |
rs543854575 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844707 | GTGCTCTCCTGCGTT[A/G]GCGCTCCTTCCGCCC | 7409 |
rs543866232 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781383 | TCTCTGCCGCCTCCC[C/T]GACAGACGGTTCTGT | 7409 |
rs543912685 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836822 | CAGAGTGACCATTGA[A/G]CAGAGAGATGGACAC | 7409 |
rs543935533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810020 | TACAAAAAATAAAAA[C/T]AAAAATAACGTTATC | 7409 |
rs544072658 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824818 | TGCAGGCGTGAGCCA[A/C]CGCACCTGGCCGGAC | 7409 |
rs544093655 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6844400 | TTTTATATTTTCAGT[-/A]AAGACAGAGTTTCAC | 7409 |
rs544113310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818771 | GGGAGAAGGTGGCTG[C/T]CTACTGAAATGAGCC | 7409 |
rs544128528 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855638 | ATTTCTATCTGTGCA[A/T]CCATCCATCTATCCA | 7409 |
rs544140540 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787028 | GCTGTCTATTTTTTT[G/T]TTTTTTTGAGATGGA | 7409 |
rs544166880 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776737 | ATCCATGGATCCATC[C/T]ATCCACTAATCTGTC | 7409 |
rs544248145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856683 | AAGCTGAGATTGCGC[C/T]ATTGCACTCCAGCCT | 7409 |
rs544259261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804088 | GAAAGGGGGTATGGA[C/T]AGGCAGAGCATGGAA | 7409 |
rs544284103 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843560 | TGGCTTTTGGAGCCC[A/G]CTGACCTGGATTCAA | 7409 |
rs544292854 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856487 | AGCACTCTGGGAGGC[C/T]GAGATGGGCAGATCA | 7409 |
rs544296020 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809263 | TTCATTTGTAGAGAC[A/G]GGGTCTTGCTTTGTT | 7409 |
rs544364669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838283 | TCTATCCATCTATTC[A/G]TCATCTACATATTAT | 7409 |
rs544365148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775894 | AAAGGTGTGCAGGCT[A/G]GAATGAGAATTCTTC | 7409 |
rs544437888 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6830913 | GGCAACATAGGGAGA[A/T]CCCCGTCTCTACAAA | 7409 |
rs544453747 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6804563 | CTGGGATTACAGGCG[C/G]GTGCCACCACGCCTG | 7409 |
rs544477173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834897 | GAGTTTGAGACAAGC[A/G]TGGGCAACAGAACGA | 7409 |
rs544479446 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6839281 | CTGGTCTTGAACTCC[C/T]GGGCTCAAGCAATCC | 7409 |
rs544481919 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6838988 | GCTCATTGCAACCTC[C/T]GCCTTCCGGTTTCAA | 7409 |
rs544485374 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780852 | GTGCTGGGATTACAC[A/G]TGATAGCCACCATGC | 7409 |
rs544542963 | snp | C/G | 0.000115545 | 0.00759994 | intron-variant | VAV1 | GRCh38.p7 | 19:6857028 | TGTGCAGAGGTTGCA[C/G]TGATGAACTCCTCGT | 7409 |
rs544576755 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795503 | ATTTATTGAATTAAT[A/T]TTATTTATAACTCTA | 7409 |
rs544637935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825678 | TGAGGGTTGACTATA[C/T]GGATGCACACAGGGC | 7409 |
rs544642375 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776918 | ACCCGCCACCACGCC[C/T]GGCTAATTTTATATT | 7409 |
rs544655196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824316 | TCAATCTCTTATCTT[C/T]CCCCGGTCCATGGCA | 7409 |
rs544727488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6818408 | TCACCTCCCTATCCT[C/T]CCCTCTTCTTCCTCC | 7409 |
rs544774993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830144 | GCTCACCGCAACCTC[C/T]GCCTCCTGGGTTCAA | 7409 |
rs544921560 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782888 | ATCCTGTCTCGGAAG[-/A]AAAAAAAAAAAGGCC | 7409 |
rs544945983 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792646 | TGACATCCTGGGCTC[A/G]GGTGATCCTCCCATC | 7409 |
rs545024406 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780098 | CCTGGGCGACAGAGC[A/G]AGACTCTGTCTTAAA | 7409 |
rs545031008 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786430 | TCCTGCCACTGCACT[C/G]CAGCCTGGGCAACAC | 7409 |
rs545043359 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6832009 | GGGCTTGCCTGTTCC[C/T]TACAGAGGGAGGGGT | 7409 |
rs545074244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775060 | CATGAGCCACCATGC[C/T]CGGCCCTTCTGTTTC | 7409 |
rs545103098 | in-del | -/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6797321 | CCTTTGCTTGGAGCC[-/T]TTTTACCCCCTTCAC | 7409 |
rs545105105 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835675 | ATCTGACGTAATGAC[A/G]GTGAGATGCATTGAT | 7409 |
rs545128289 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787770 | GCCCAACTGTTTTTT[A/T]AATGTTTTAAAAACA | 7409 |
rs545197079 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836052 | CTAATTTCTGTAGTT[G/T]TAGTAGAGATGGGGT | 7409 |
rs545215770 | snp | C/T | 4.95037e-05 | 0.00497488 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6850679 | TTCCAGATATAACGT[C/T]GAGGTCAAGCACATT | 7409 |
rs545290109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786192 | AACACCACCTGGCAC[A/G]TAGTACGGAATCAAT | 7409 |
rs545294664 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775856 | AAAAGGAAAGGTGCT[C/T]CTGTGGAGGAAATGG | 7409 |
rs545304797 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6814860 | TCAACATCTCATTAT[C/T]AAGTACAGTGTTTCG | 7409 |
rs545391453 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6804855 | CAGCCTCCCAAGTAG[C/G]TGGGACTACAGGCGC | 7409 |
rs545391871 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843919 | AGTGTTCTTTCATAA[C/T]GGCACATAAAAGAAT | 7409 |
rs545394711 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831543 | GGTCTCAAACTCCTG[A/C]CCTCGTGATCCGCCC | 7409 |
rs545496044 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771562 | GATCGAGACCACGAT[A/G]AAACCCTGTCTCTAC | 7409 |
rs545502808 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6805289 | AATTAGCTGGGTATG[C/G]TGGCACACACCTGTG | 7409 |
rs545636356 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841020 | TGACCTGAGGTGATC[C/T]GCCCGCGTTGGCCTC | 7409 |
rs545650423 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6808726 | GTAACAAACAGTCCC[C/T]TAAAATGGAATGGCT | 7409 |
rs545670381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777048 | GTGTGAGCCATACGC[C/T]CGGCCCATCCATTCA | 7409 |
rs545670947 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6798286 | TGTCTCAAAAAAAAA[A/T]ATATGATTTGGTAAA | 7409 |
rs545677496 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837480 | TCTCTGCTTGATGGA[A/C]CCCTCGCTCTTCATG | 7409 |
rs545731608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776780 | TTGTTTATTTATTTA[C/T]GGCGTCTCACTCTGT | 7409 |
rs545734935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852582 | AAAAATTAGCTGGGC[A/G]TAGTGGCGGGCGCCT | 7409 |
rs545744867 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772020 | TTTGAGCAAAGACAT[A/G]TAGGGGTGAGGGAGC | 7409 |
rs545752129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817265 | AATGGGGTTTCACCA[C/T]GTTGCCCAGGCTGGT | 7409 |
rs545772702 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808313 | GTGAGACTTCATCTC[-/A]AAAAAAAAAGTTCAA | 7409 |
rs545773979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852347 | TGTAAATTAAGGCAT[G/T]TGGCCCCATAGAAGG | 7409 |
rs545779697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811197 | TGCACCACCATGCCC[A/G]GCTAATTTTTGTATT | 7409 |
rs545821287 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844989 | GATTCTGTCTTTATT[A/C]AAAATGTTGATGTTT | 7409 |
rs545834293 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809958 | AGCTAATTGTTTGAG[G/T]CCAGGAGTTCAAAAC | 7409 |
rs545863264 | snp | C/T | 0.190519 | 0.242821 | intron-variant | VAV1 | GRCh38.p7 | 19:6832620 | CTATTCCTCCTCCAC[C/T]TCTTCTTCCTCCTCC | 7409 |
rs545893180 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804191 | ATCCAGAGAATGTGA[C/T]GCACGGCAGGCAAGC | 7409 |
rs545909379 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839570 | ACCACGCCCGGCTGG[C/G]TATGGCATTTTCTTT | 7409 |
rs545917989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817684 | GAAATTTTAATTAAT[A/T]TATGTATATATTTAT | 7409 |
rs545945226 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6815711 | CCTGAGTTTGTATCC[C/T]GGCTGTGTGTCTCAC | 7409 |
rs545946170 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | VAV1 | GRCh38.p7 | 19:6845714 | TATATTATATTATAC[A/C]ATACACAATATATTA | 7409 |
rs545953573 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793649 | AGCCTATAATTTGTA[C/T]GATAACATCAAGTTT | 7409 |
rs545962491 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831238 | TTCCTTACTTCCTTC[C/T]GCTTTTTCTCCTGTG | 7409 |
rs546004141 | in-del | -/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6822132 | CACCCTTGGAGTCTT[-/G]GGGGGGACAAAGCCC | 7409 |
rs546056863 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771249 | CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 7409 |
rs546072863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794851 | TAGTGATGATGGTGC[C/T]TCAGCTCCATGGTGA | 7409 |
rs546095781 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855723 | CACCAGTCCATTAAT[G/T]CATCCATCCATCCAT | 7409 |
rs546110418 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6851344 | TGCCTGGCTAATTTT[A/T]AAAAAAAATTTTTTT | 7409 |
rs546133498 | in-del | -/A | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6823521 | ATATATATTTTATAT[-/A]TATTTTTTGTTATGT | 7409 |
rs546157297 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831432 | TTCTCCTACCTCAGC[C/T]TCCTGAGTAGCTGGG | 7409 |
rs546209856 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789697 | CCGCATCATGGGTTC[A/G]AGTGATTCTCCTGCC | 7409 |
rs546220398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6809457 | CAGAGGCAACCTTAT[A/G]TATGAGACCTGGAGA | 7409 |
rs546272589 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6804113 | ATGGAAGCTTTCCAC[A/G]GCAGTGAAAATACTC | 7409 |
rs546347446 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | VAV1 | GRCh38.p7 | 19:6814686 | CCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 7409 |
rs546349041 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6833429 | CGTCACTCTCCTGAT[C/T]TAAAGAGAACCCAAG | 7409 |
rs546358042 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778290 | AGATGGAACTTGAAG[G/T]CCAAGAGACTGGAGA | 7409 |
rs546405984 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6773285 | TAACTCTCTCAAGCC[C/T]CAGGCGCCTCTACTG | 7409 |
rs546413655 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6837798 | TGAGTTTGCAGACGA[C/T]GTTCCCCTTTACCCC | 7409 |
rs546433398 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814051 | GGTGACAGAGTGATA[A/C]CCTGTCTCTAAAAAT | 7409 |
rs546445094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790035 | ACAAAAAAATTAGCC[A/G]GCCATGGTGGCAGGC | 7409 |
rs546488728 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6783536 | CTGGAGTGCAATGGC[A/G]CGATCTCTGTTCAGT | 7409 |
rs546510663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808781 | TTAATTTAGTAAATT[A/G]TCTGGGCAGATAGGT | 7409 |
rs546512859 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791157 | GGTGGGTCTTAAATA[G/T]CTCCTCATCTTGAAG | 7409 |
rs546524231 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6818869 | ACCTGTAATCCCAGC[A/C]CTTTGGGAGGCCGAG | 7409 |
rs546626489 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775392 | TTGGATGAAGGACGA[A/G]GGTGCATGATGCTAA | 7409 |
rs546647855 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845173 | ATCACTTGAGGTCAG[A/G]AGTTCAAGACCAGCC | 7409 |
rs546696913 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840367 | CTGGAGAGCAGTGGC[A/G]CAATCTTGGCTCACT | 7409 |
rs546731572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852478 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCA | 7409 |
rs546736372 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771444 | ACGAGAGTGAAACTC[C/T]GTCTCAAAAGAAAAA | 7409 |
rs546754097 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852778 | GTGGTCCCTTCCCCA[C/T]AAATAGTCCTGGCTG | 7409 |
rs546802612 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6825216 | GGGTTGGGAGTTGAG[C/T]GGCATGGGGCGGGTG | 7409 |
rs546802692 | snp | C/G | 7.0599e-05 | 0.00594092 | intron-variant | VAV1 | GRCh38.p7 | 19:6832239 | TTTCTGTCCACAGAG[C/G]GGCAGGGGCTGGGAA | 7409 |
rs546832235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842965 | TGGGGCAGTCTCTCC[C/T]CCGAGGTTCTGGGAC | 7409 |
rs546932288 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816299 | TGCTGGGATTACAGG[C/T]GTGAGCCACCATGCC | 7409 |
rs546965984 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799460 | GGCGTGAGCCACCAT[A/G]CCCGGCCTATACTTT | 7409 |
rs546974925 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810475 | TTGAGAGGCAGAGGT[C/G]GGTGGATCCCCTGAG | 7409 |
rs547032240 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782846 | ATAGATCGCGCCGCT[A/G]CAGTCCAGCCCGGGT | 7409 |
rs547058188 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771667 | GAATGGCGTGAACCC[A/G]GGAAGCGGAGCTTGC | 7409 |
rs547060902 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784235 | GTACTCCAGACTGGA[C/G]AAAAGAGTAAGACCC | 7409 |
rs547119669 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777298 | ATCCAGCAATGACAA[G/T]GTCTGCCAGGCCCTG | 7409 |
rs547134456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810938 | CAAAGAAATGGATTG[C/T]AATGAAAAGGCATGC | 7409 |
rs547136432 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6804776 | TCGCACAGGCTGGAG[C/T]GCAGTGGCGCAATCT | 7409 |
rs547140063 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6819523 | AGGTTCATCCATGTT[A/G]TAGTGTGGAACAGTA | 7409 |
rs547162058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816879 | TGAGGTGGGAGAACC[G/T]CTTGAACCTGGGAGG | 7409 |
rs547256197 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799970 | GCCTGGTAATGGAAT[A/G]TATCGTATGATAGGT | 7409 |
rs547349432 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781299 | TAGATATTGCCAAAT[C/T]GTTATCCGTCTGGGA | 7409 |
rs547351815 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | VAV1 | GRCh38.p7 | 19:6788468 | ACCTCCACCTCCTGG[G/T]TTCAAGTAATTCTTG | 7409 |
rs547393017 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6794526 | AAACAAAAAAACAAA[C/G]AGGATAACCAGATGG | 7409 |
rs547401675 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781760 | TTACAGGTGTGCGCC[A/G]AGATGCCCAGCTAAT | 7409 |
rs547421757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806961 | TCTACTGGGATTCCA[C/T]GATCTGTTCAGACAG | 7409 |
rs547428166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801248 | TGGGTTTCACACCAG[A/G]CTCTACCGCAAACAT | 7409 |
rs547497960 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6821922 | GGGGGTGGAGGGTGT[G/T]GGGGGACATGGCCTT | 7409 |
rs547625648 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795056 | AAACCCGGAGAGAGA[C/G]CAAGTATTCCTCAAA | 7409 |
rs547644289 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804966 | CTGACCTTCCTGAGG[C/T]GTGAACCACCCGCCT | 7409 |
rs547678560 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840305 | CAGAATTTTCTTTCT[-/T]TTTTTTTTTTTTTTT | 7409 |
rs547684621 | snp | A/C | 0.00119737 | 0.0244387 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772629 | CTGCAGGTGCTCCCC[A/C]AGCTCCCCCCCGCCC | 7409 |
rs547702771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839748 | CCAGGCTGGAGTGCA[A/G]TGGTGCAATCTTGGC | 7409 |
rs547709144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826334 | CAAGCGTGAAACCCC[A/G]TCTCAAAAATAAATA | 7409 |
rs547732071 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832637 | CTTCTTCCTCCTCCT[C/T]CCTTTCCTCCCCTTC | 7409 |
rs547784896 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6850501 | GGAAGACATTAAGGC[-/T]TTAGAGTAGCAAAGG | 7409 |
rs547872444 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801811 | AAGGAGCGTGGAAAG[C/T]CAGCCGACCTTTCTG | 7409 |
rs547904798 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834624 | ATATTAATATTAATT[A/G]ATATAATATAGTAAT | 7409 |
rs547927729 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803377 | GAGTAGTAGCTGCTG[A/G]TGTTACCATCACAAT | 7409 |
rs547927828 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785314 | AGTGCTCGGATACAG[A/G]CATGAGCCACTTCAC | 7409 |
rs547985310 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771422 | CCACTGCACTCTAGC[C/T]TGGGCAACGAGAGTG | 7409 |
rs547991756 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6853872 | CTGGAGTTACTGTCC[C/T]GAGAGCTTGTGCCCC | 7409 |
rs548016939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789362 | GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTCCC | 7409 |
rs548046777 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841764 | CAGGCATGAGCCACC[C/G]TGTCCAGCACATACT | 7409 |
rs548052155 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819857 | TGGCAAATGCAAGAA[C/T]ACAAAGGTTTCTTTC | 7409 |
rs548073954 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6804763 | GAGTCTTGCTCTGTC[A/G]CACAGGCTGGAGTGC | 7409 |
rs548096504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844729 | CTTCCGCCCTTCTGC[G/T]CCGAGATGTGGTCAA | 7409 |
rs548153352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847323 | GTTGCTCCTGCCTCC[C/T]GCAGCCCCCGGGAAC | 7409 |
rs548211384 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | VAV1 | GRCh38.p7 | 19:6832671 | CTCCTCCTCCTCCTC[C/T]TCCTCCTCTTCTTTC | 7409 |
rs548273582 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6800766 | AGCTGGGATTACAGG[C/T]GCCTGTCACCACGCC | 7409 |
rs548317311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839878 | TGTATTTTTCGTAGC[A/G]ATGGGGTTTTGCCAT | 7409 |
rs548354906 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787113 | CAGGGGCTCAGGCAA[A/T]ATCTCAGGACACCTC | 7409 |
rs548392992 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835946 | GCATGATCTCAGCTC[A/T]CTGAAACCTCTGCCT | 7409 |
rs548467392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804880 | AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT | 7409 |
rs548530246 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6838660 | CCATCACCTGTCTGT[G/T]TATCATCTATCATCT | 7409 |
rs548548173 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6854568 | AATAAAAATAAAAAC[A/G]AAAACATTAGTTGGG | 7409 |
rs548553561 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6806276 | ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTT | 7409 |
rs548599607 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6785754 | AACCTCTGCCTCCTG[C/G]GCCCAAATGATTCTC | 7409 |
rs548636121 | in-del | -/TCAGTAGC | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6806473 | TAAGTATGGCTTCAT[-/TCAGTAGC]TCCAACAATGTCATC | 7409 |
rs548640895 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6849496 | AGTGGGGTGGGGGGT[-/G]GGGGGAAAGTTTCAC | 7409 |
rs548655874 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6817971 | GATTACAGGCATGAG[C/T]CACCACGCCCAGCCT | 7409 |
rs548660708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795424 | TTGAAGACCAGAGGA[A/G]ACAGTTGTAATGCAC | 7409 |
rs548714131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773491 | GGGCCCCTTCCTTCC[C/T]CTTACATCTTCCTTC | 7409 |
rs548776604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6827692 | CCATCTCTGCCTCCC[A/G]GGTTCAAGCAATTCT | 7409 |
rs548805949 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821399 | GAGTGAGACTCCGTT[A/T]AAAAAAATACTAAAA | 7409 |
rs548807366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777496 | AGGGGGGCACTTTGA[C/T]GAGGAGGGCTAGTGG | 7409 |
rs548849280 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | VAV1 | GRCh38.p7 | 19:6779908 | CAAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA | 7409 |
rs548877672 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822022 | ACAGCCCTGCCCTGG[A/G]GTCTTGGGGGACATG | 7409 |
rs548883106 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772555 | TGCCCAGGCCTGTGT[C/T]GAGTGGGCGGAAGAA | 7409 |
rs549039418 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6784530 | ACAGAGTTTCACTCT[C/G]TCTCCCAGGCTGGAG | 7409 |
rs549080898 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802820 | ATGGGCAGTATCCCC[A/T]CTCTGAGCCTCAGTT | 7409 |
rs549117514 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6813322 | CACAACATGGTCGCC[A/G]GTGAGTGGTCCAAGA | 7409 |
rs549119499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775096 | TGCCAGGGGATTACA[C/G]TGTCCTCAGCTGGGA | 7409 |
rs549144142 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827142 | CAGGGCAGGGGTGGT[A/G]AGGACGGGGGCTCTC | 7409 |
rs549194174 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824459 | GTTTTCAAGGTTCAT[C/T]CACATTGTAGCCTGT | 7409 |
rs549194948 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790240 | GAAGACTCATTTGAT[A/G]TTATTTTATCATCAG | 7409 |
rs549224464 | in-del | -/G | 0.00199481 | 0.0315187 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772416 | GGACCAGACAGAGGA[-/G]GGGGTGAGAAGTGGG | 7409 |
rs549224502 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6791711 | AACAAATAGACAAAA[C/T]GCTGGCACATTGTAA | 7409 |
rs549237745 | snp | C/G/T | 0.000525996 | 0.0162099 | intron-variant | VAV1 | GRCh38.p7 | 19:6822338 | CATGCCGGTGCGTGA[C/G/T]GTGGAGGGTCGGGCC | 7409 |
rs549259883 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6836315 | TTCTCCACGTCCTTG[-/T]CAACACTTAGTATTG | 7409 |
rs549331674 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6824039 | AACTCCTGGGCTCAA[A/G]TGATCCCCCTGCCTT | 7409 |
rs549408247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6830539 | CTGGCTCCCAGGTTC[A/G]AGCAATTCTCCTGCC | 7409 |
rs549434212 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6779204 | CTACAGGTGTGCACC[A/G]GCAATACCTGGCTAA | 7409 |
rs549439945 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6818514 | CCATTGCATGCACTG[C/T]TCTCTCTTCTTGGAA | 7409 |
rs549447294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842097 | CGGGCGTGGTGACAC[A/G]CACCTGTAATCCCAG | 7409 |
rs549469920 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839622 | GAACTAGGTAGAGGC[A/G]GTGATTCCTCATTCA | 7409 |
rs549531642 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841717 | CTGACCTCGTGATCC[A/G]CCTGCCTCGGCCTCC | 7409 |
rs549576760 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841726 | TGATCCGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 7409 |
rs549618025 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783818 | GCTCCATTTAACTAC[A/G]AGGGAGACTAGGAAT | 7409 |
rs549622954 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812141 | TGGGCAGCCATTTTC[C/G]AGCAGCAATTCCATA | 7409 |
rs549632949 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6780814 | CCTGACCTCAGATGA[C/T]CTGCCCGCCTCAGCC | 7409 |
rs549637086 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785106 | CTTCCTTCTTCAGGG[A/T]TTTCTCTTCCCTCAG | 7409 |
rs549697178 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829614 | AAGACTGACAGGCAG[C/T]AGGGCCAATGCGGAT | 7409 |
rs549738453 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784434 | CCTGCTAGGGCCAAC[A/T]GGAGGGGCATCTAGG | 7409 |
rs549740813 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6796562 | CTCAGAGCCTTTGCA[C/T]TAACCTCAGGGCTTC | 7409 |
rs549749729 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6817516 | CCTCCTACACATAAG[C/G]TACTATCATAGTTGC | 7409 |
rs549800733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802207 | GGGTCGGGGAAGTGG[A/G]GAGGGATAACATTAG | 7409 |
rs549905370 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6791136 | TGGATGATCCCAGAT[A/G]GCCTGGGTGGGTCTT | 7409 |
rs549916293 | snp | C/T | 3.29506e-05 | 0.00405884 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833712 | TTACCCTCCCGTAGA[C/T]TTCCCAGGAACTATG | 7409 |
rs549916706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817811 | CCTCTCTCAGCCTCC[A/C]GAGTAGCTGGGACTA | 7409 |
rs549960414 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792170 | CATCCTGGGCAACAT[A/G]GTGAGATCCCACCTC | 7409 |
rs549968050 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773406 | ACTCCTTTGACCCCC[A/C]GAGTCTGGATGTGGG | 7409 |
rs549978086 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6801118 | GGCTGGATTACATAA[A/G]CCCTGTAAGGGCAGA | 7409 |
rs550075674 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821545 | CTAGCGCCTCAGACA[C/G]AGCCTTGCAGCTGGA | 7409 |
rs550117437 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | VAV1 | GRCh38.p7 | 19:6829593 | GCGAGGGGTATGGGT[A/G]GAGCGAAGACTGACA | 7409 |
rs550128466 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6840052 | TCACAGTGTTTTGCC[A/G]CCATCACCACCATCA | 7409 |
rs550174359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842216 | GCCTGGGCAATAAGA[A/G]CAAAACTCTGTCTCA | 7409 |
rs550181298 | in-del | -/TTTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815141 | ACAGTTGCTTCTTCT[-/TTTA]TTTATTTATTTATTT | 7409 |
rs550188686 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6814640 | TCTTTTCTTTCTCTC[C/T]TTCCTTCCTTCCTTC | 7409 |
rs550201391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785901 | TGACTTCAAGTGATC[C/T]GCCCGTCTCGGCCTC | 7409 |
rs550203890 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835142 | CAGTCAGCTTTCTTA[A/G]CAAGAGTCAAAATTA | 7409 |
rs550235122 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6848654 | GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGT | 7409 |
rs550262735 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6791619 | TCTCCAAAAAATGTT[C/T]ACAGGTCACCTTCAC | 7409 |
rs550288646 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6842869 | TTTGATTTTTGCCAA[A/C]CATCTAAAAATGTAA | 7409 |
rs550295604 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808765 | ATATTTGTTATTCCA[A/G]TTAATTTAGTAAATT | 7409 |
rs550311229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818453 | TCCAGCCACATGGGC[C/T]TCCTTGCTGTTCCTC | 7409 |
rs550363974 | snp | A/C/G | 0.000142535 | 0.0084409 | intron-variant | VAV1 | GRCh38.p7 | 19:6847959 | TGGGGACCCAGGCAC[A/C/G]GGGACCGTGCCACCT | 7409 |
rs550376004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812866 | GATAAGAATGGTGAT[A/G]AGGAGAATGGTGATG | 7409 |
rs550406018 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803596 | AGAGATGGACTTTTG[C/T]CCTTGTTGTCCAGGC | 7409 |
rs550484335 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834634 | TAATTAATATAATAT[A/G]GTAATAATATATTAT | 7409 |
rs550486635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841637 | GCGTCACCACGCCCG[A/G]CTAATTTTTTGTATT | 7409 |
rs550491909 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6786228 | TATTCATTTATCATA[A/T]GAATATATGATTCTA | 7409 |
rs550521455 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6841084 | TGCCGGGCCTAATTT[C/T]TGTATTCTTTTGTAG | 7409 |
rs550530205 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814697 | TTCTTTCTTTCTTTC[C/T]TTCTTTCTTTCTTTC | 7409 |
rs550536067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803172 | ACTGAAGTGAAAGTG[C/T]ATAGCGGCAGTTGCA | 7409 |
rs550665036 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829543 | CCCATCCAGAGAAGG[C/T]GGTGGAGCCTTGATG | 7409 |
rs550708322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776197 | ATCCATCCATCCACT[C/T]CTCCATCCATCTGCT | 7409 |
rs550709528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6781797 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCATGTT | 7409 |
rs550726453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831603 | AGGTGTAAGCCACCG[C/T]GCCCGGCTGGCTTCT | 7409 |
rs550727494 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831890 | TGTGTGCATGTGCAC[A/G]CCTGCGTATGTGGTT | 7409 |
rs550760625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851648 | ATCATTTCAGCAACA[A/G]CTCAAATGCCTTTTG | 7409 |
rs550763015 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6821689 | GGATCATGTGAGTAA[C/T]CACCTGGGCCTTGGG | 7409 |
rs550786729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779972 | AAAAATTAGCCGGGC[A/G]TGGTTGCGGGCGCCT | 7409 |
rs550813000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6849532 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 7409 |
rs550816660 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836131 | TTCCTGCCTCGGCCT[C/T]CCAAAGTGCTGGGAT | 7409 |
rs550853957 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856250 | TGTGGTGAGCTGAGA[C/T]CGCGCCACTGCACTC | 7409 |
rs550859994 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | VAV1 | GRCh38.p7 | 19:6774420 | GGTGTGAGCCACCGC[A/G]CCCAGCCTTTTTTTT | 7409 |
rs550886352 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6848858 | GAGTGCAGTGGTGAG[A/G]TCTTAGCTCACTGCA | 7409 |
rs550903275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819917 | GCTGGGGCCATGTTA[A/C]ATGTGCCCAGCTGTT | 7409 |
rs550923312 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780435 | TACATTTACATAAAC[C/G]TAGAGGGTACAGCAT | 7409 |
rs551051124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813825 | TTGAGAGCCTGTGGT[A/G]GGAGAGTCACTTGAG | 7409 |
rs551058843 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | VAV1 | GRCh38.p7 | 19:6788040 | CGAGATCCCGCCACT[A/G]CACTCCAGCCTGGGT | 7409 |
rs551070952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809634 | GGATGATGGGGGAAC[C/T]ATGGCAAGGTTTCAA | 7409 |
rs551076505 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817433 | TCAGAATCACCTGAG[A/G]AGAGTGTTAATATGC | 7409 |
rs551109208 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815745 | AGTTTCCTTCTCTGT[A/G]AAATGAGGATAATAA | 7409 |
rs551110298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855851 | TCTATCTATCCATTC[A/G]TTATCTATCTACCTA | 7409 |
rs551117999 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824674 | GTAGCTGGGATCACA[C/T]GCATCTGCCACCGTG | 7409 |
rs551135411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6823239 | CAAGCAATCCTTCTG[A/C]TTCAGCCTCCCAAGT | 7409 |
rs551137873 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814801 | TGAATAGAAATGGTG[A/G]TAGCAGGTTCCGTTG | 7409 |
rs551168328 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6829376 | GCCAGGCTCCTAGAT[G/T]GACAGGTGGGTGGAG | 7409 |
rs551172306 | snp | A/C | 0.00285655 | 0.0376844 | intron-variant | VAV1 | GRCh38.p7 | 19:6822369 | TGGGGAGGGCGTGGG[A/C]GGGGGGCAGCCCCAG | 7409 |
rs551176116 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6824000 | TGGAGTGCAGTGGCA[C/T]GATCATAGTTCACTG | 7409 |
rs551195769 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792977 | GGACTCCAGTTGTGT[G/T]GGGGGTCCAGGTTCC | 7409 |
rs551261600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817877 | GTTTTTAGTAGAGAC[A/G]GGATTTCACCGTGTT | 7409 |
rs551346204 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832365 | AAGGCTGTCTTCATC[C/G]TTGGAATGCAGGGGT | 7409 |
rs551428435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6781710 | CCTCCCAGGTTCAAG[C/T]GATTCTCGTGCCTCA | 7409 |
rs551445304 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810683 | GCACTCTGGCCTGGG[C/T]GACAAGAGTGAAACG | 7409 |
rs551485976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781079 | AAGCCCACCATTTTT[C/T]AAAGTAGAGATGGGG | 7409 |
rs551514215 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792982 | CCAGTTGTGTGGGGG[G/T]TCCAGGTTCCAGTCA | 7409 |
rs551514318 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812772 | TGGTCATGAATACTA[C/T]TGTGGTAATGATGGT | 7409 |
rs551524169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808243 | CTTGAACCCAGGAGG[C/T]GGAGTTTGCAGTGAG | 7409 |
rs551543184 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856962 | AGAGCAGGTGCAAAG[G/T]CCCTGAGGTGGGAGG | 7409 |
rs551549782 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814718 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCC | 7409 |
rs551578307 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827024 | CCAAGTCGGGCTGAG[C/T]TCCCACTTCTCACTG | 7409 |
rs551596145 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774744 | CGGCTGCTCCTTCTG[-/T]TTTTTTTTTATCTTA | 7409 |
rs551621372 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795602 | TACGTAACGGTTTAC[C/T]ATGTCCTGGCACAGG | 7409 |
rs551666697 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779922 | CGAGACCATCCTGGC[A/T]AACACGGTGAAACCC | 7409 |
rs551670543 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839366 | CAGCATAAAACTGAC[C/T]GTTACAATGAAAAAT | 7409 |
rs551728854 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6785784 | CCTGCCTCAGCCTTC[C/T]GAGTAGCCAGGATTA | 7409 |
rs551733116 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799217 | CTGTCGCCCAGGCTG[C/G]AGTGCAGTGGCGCAA | 7409 |
rs551773613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818949 | GGTGAAACCTCATCT[C/G]TACTAAAAATACAAA | 7409 |
rs551794829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6798664 | TTTCTCCCCTTCCCC[C/T]CCCCACCCAAAAGAA | 7409 |
rs551803666 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6797740 | CAAGAGTGAAACTCC[A/G]TCTAAAAAAAAAAAA | 7409 |
rs551815441 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775635 | TTCGAGGGGGCACAT[C/T]CCTGCCCCTACCCAT | 7409 |
rs551819958 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6836898 | TGATGGGGCAGGATC[A/C]ACGTGTAGGGTTATG | 7409 |
rs551833670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825859 | GTGAAACCCCGTCTC[C/T]ATCGCCTAAAAATAC | 7409 |
rs551838003 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV1 | GRCh38.p7 | 19:6814698 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 7409 |
rs551857576 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6850244 | TTTTTTTTTTTTTTT[G/T]TGTGATCTAGTTTGC | 7409 |
rs551890647 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6819403 | CCCTACTGACACCTT[C/G]ATCTTGGACTTCTAG | 7409 |
rs552004464 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803983 | CCAGTCCCAAAAGGC[C/T]ACATACTATATGATA | 7409 |
rs552076353 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804195 | AGAGAATGTGACGCA[C/T]GGCAGGCAAGCCCCA | 7409 |
rs552084554 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830593 | TACGGGCACCCACCA[A/C]CATGCCCAGCTAAAT | 7409 |
rs552154002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831782 | CAGCAGGTGCTGCAC[C/T]AATGCTTTGTTGAAC | 7409 |
rs552207618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838532 | ATTATCTATCATCTA[C/T]CTATTCACCGATCAT | 7409 |
rs552289882 | snp | C/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771770 | GAAGAAAGAAACAAA[C/G]AGAGAAAGAAAGGAA | 7409 |
rs552306451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6820889 | CTACACTGGGCAAGC[C/T]AAGGACTGTCAGGGG | 7409 |
rs552338733 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810993 | TGTCCTCATCTGGAA[C/T]GGAGGTACAGACTGT | 7409 |
rs552397765 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808910 | TTTAGCTAGGTGCTT[C/G]TCTCTGCTCCACACG | 7409 |
rs552439360 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816336 | CAAAAACATTTTTAA[A/G]ATTAGCTGGATGTGG | 7409 |
rs552440200 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6837933 | TGTATTTAAATGTTG[A/T]CAATTTCCCCAAAAA | 7409 |
rs552492238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844520 | CCTCGCCCAGCCGAC[A/G]CTCCCATCTTCTAAG | 7409 |
rs552505918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811510 | TAAGGGAGGCTGCAG[C/T]TGGGGGAGAATGAGG | 7409 |
rs552519263 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843614 | CTGTATGACCTTGGG[C/T]CGGTTACTTAACCTC | 7409 |
rs552563453 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852913 | TTCCTAGCTCTGCCC[C/G]CTTATGGGCTGGCCC | 7409 |
rs552568996 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6830842 | CCTGTAATCCCAGTA[C/T]TTTGGGAGGCCGAGG | 7409 |
rs552602299 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840506 | GAGTTTCACCGTGTT[A/G]GCCAGGATGGTCTCG | 7409 |
rs552642203 | in-del | -/CC | 0.039431 | 0.134762 | intron-variant | VAV1 | GRCh38.p7 | 19:6798660 | CTGTTTCTCCCCTTC[-/CC]CCCCCCCCACCCAAA | 7409 |
rs552704899 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820913 | TCAGGGGACAGGCAG[A/T]CAAGCCAGACCAGGC | 7409 |
rs552705151 | in-del | -/A | 0.0197687 | 0.0974348 | intron-variant | VAV1 | GRCh38.p7 | 19:6845226 | CTCTACTAAAAATAC[-/A]AAAAAAAAATTAGCT | 7409 |
rs552705172 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800111 | GAGACCAACCTGACC[A/C/G]ACATAGTGAGGCTCT | 7409 |
rs552708170 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808434 | CACTCTATGTAGCAG[A/G]GAACCAAAGTAACAA | 7409 |
rs552726269 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789285 | TTTGACAGAGTCTCA[C/T]TCTGTCGCCCAGGCT | 7409 |
rs552735452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797424 | TAGGAGCAAAATGGC[C/T]GGGCACAGTGGCTCA | 7409 |
rs552776543 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779850 | GGCACGGTGACTCAC[A/G]CCTGTAATTCCAGCA | 7409 |
rs552809846 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789654 | TCAGACTGGACTACA[A/G]TGGTGTGATCTTGGC | 7409 |
rs552861419 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856913 | TCAGCCTTGTGTACG[C/T]TGGGTGATGTGTTTT | 7409 |
rs552896127 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818287 | TTGGCAAGGAACTTT[C/T]TTCTGGATATCAGGG | 7409 |
rs553062897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786915 | AAAAACTTCTCTAGT[A/G]ACAATCTATATAAAA | 7409 |
rs553065003 | snp | A/C/T | 0.00158039 | 0.0280663 | intron-variant | VAV1 | GRCh38.p7 | 19:6833700 | TCACCATTTCCTTTA[A/C/T]CCTCCCGTAGATTTC | 7409 |
rs553128227 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850317 | TCTATTTCCACCATG[G/T]TGACAGAAATGGGTC | 7409 |
rs553143675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856597 | GGTGTGGTGGCAGGC[A/G]CCTGTAATCCCAGCT | 7409 |
rs553183439 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6849579 | CGGCCTCTCAAAGTG[C/T]TGGGATTACAGGCGT | 7409 |
rs553236092 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838126 | CTATCTATCTATCTA[G/T]CTATCTATCCATGCA | 7409 |
rs553260888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814818 | AGCAGGTTCCGTTGC[A/G]TAGTTCTGATTTCAA | 7409 |
rs553279855 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835910 | AGAGTCTCACTCCAT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs553289039 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6781254 | TTTTATTTTGTCAAC[C/T]GAAGTGCTAGCCAAT | 7409 |
rs553297584 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819088 | ACCATTGCACTCCAG[A/C]CTGGCGGACAAAGTG | 7409 |
rs553339573 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810037 | AAAATAACGTTATCT[G/T]GGCATGGTGGTGCAT | 7409 |
rs553343828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783245 | CAAATTACATGACTT[C/T]AGTGATAGTGAGACT | 7409 |
rs553361058 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6804359 | TGACTGCTCTTGCAG[G/T]GCTACCCCACAGGCT | 7409 |
rs553390638 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6838773 | CTCATTCTGTCACCT[A/C]GGCTGGAGTGCAATG | 7409 |
rs553424863 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775830 | CCATGGGATGTGAAA[C/G]GGTAGAGGGAAAAAG | 7409 |
rs553450655 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804023 | TGATGTTTCAGAAAA[A/G]GCAAAACTGTAGAAG | 7409 |
rs553450709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809815 | AGCTTAGATGTGACA[A/G]ATAGTTTGGATGTAG | 7409 |
rs553463099 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6831959 | CCTTTTACAAGGATA[A/T]CCATGCATGGTGCTA | 7409 |
rs553477984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777045 | CAGGTGTGAGCCATA[C/T]GCCCGGCCCATCCAT | 7409 |
rs553500434 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6816088 | GCAGTGGCGCAATCT[C/T]GGCTCACTGCAAGCT | 7409 |
rs553532003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6788136 | GATGGACCTCACTGT[A/G]TTGCTCAGGCTGATA | 7409 |
rs553605381 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6782899 | GAAGAAAAAAAAAAA[A/C]GGCCAGGTGCAGTGG | 7409 |
rs553613039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815348 | TGTCTCTCCGTGTTG[C/T]TCAGGCTGGTCCCAA | 7409 |
rs553697371 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840366 | GCTGGAGAGCAGTGG[C/T]GCAATCTTGGCTCAC | 7409 |
rs553702739 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816500 | TCTCTCGCTCTCTCT[C/G]TCTCTCACACGCACA | 7409 |
rs553771548 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827190 | CCATCTCCAGCCCCC[A/C]TCAGCAGGCAGAATA | 7409 |
rs553781400 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6820359 | CTCATCTCCGCCTCC[G/T]GAGTAGTTCAAAATG | 7409 |
rs553784940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852292 | GGTGCTGAGATTCCA[A/G]GCATGAGCCACTACA | 7409 |
rs553794794 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771985 | GAGGGGATTTAGGAA[A/G]ACCTCATGAGAAGGT | 7409 |
rs553847194 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6822044 | GGGGACATGGCACTG[C/T]CCTGGGGTCTTGGGG | 7409 |
rs553882037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827851 | GTGATCCTCCCGCCT[C/T]GGCCTCCCAAAGTTC | 7409 |
rs553906319 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805830 | AAAAAGAAACTAAAA[A/G]AGAGGAGGAAAGGAA | 7409 |
rs553952773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852678 | GTGAGCCGAGATTGC[A/G]CCACTGCACTCCAGC | 7409 |
rs553955602 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827822 | CCAGGCTGGTCTTGA[A/G]CTCCTGACCTCAAGT | 7409 |
rs553991948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6805184 | AATCCCAGCACTTTG[A/G]GAGGCCGAGGCGGAT | 7409 |
rs553992837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790390 | TGTAACAAAGAACCA[C/T]GGATCGGATGTCTTA | 7409 |
rs554030230 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825499 | TCAGACACCACTGGA[C/T]GGGGAGGACTTTTTG | 7409 |
rs554062564 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837986 | CCTATGGTTTCTCCA[C/G]TGTCAAGTTACAATA | 7409 |
rs554089465 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839560 | GGCGTGAGCCACCAC[A/G]CCCGGCTGGGTATGG | 7409 |
rs554140302 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6825967 | AGAATTGCTTGAACC[C/T]GGGAGGCGGAGGTTG | 7409 |
rs554144067 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798378 | GAAGCCTGTAATCTC[G/T]CCCCTTTGGGAAGCT | 7409 |
rs554171224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794847 | GGCATAGTGATGATG[A/G]TGCCTCAGCTCCATG | 7409 |
rs554180403 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795227 | CTGAACCTATCTAGG[A/G]GCAGGGTGCAAAGGA | 7409 |
rs554205545 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799981 | GAATATATCGTATGA[C/T]AGGTGCATGCTTAAT | 7409 |
rs554212460 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840695 | CTGCAGACTCGACCC[C/G]CTAAGCTTAAGTGAT | 7409 |
rs554222959 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6816059 | GAGTCTCGCTCTGTC[C/G]CCCAGGCTGGAGTGC | 7409 |
rs554262870 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | VAV1 | GRCh38.p7 | 19:6784635 | AGTAGCTGGGATTAC[A/G]GGCAAGTGCCACCAC | 7409 |
rs554267502 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6782252 | GAAGAATCCCTTGAA[C/G]CCAGGAGGCGGAGGT | 7409 |
rs554307393 | in-del | -/ATAAA | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6846156 | TGTATTTACACTTAT[-/ATAAA]ATTATATATTATGTA | 7409 |
rs554325989 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784099 | TCTCTACAAAAAATA[A/T]AAAAATAAGCCCGGC | 7409 |
rs554327020 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6793265 | TGCGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 7409 |
rs554327135 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798748 | ACTCCTGGACTCAAG[C/T]GATCCTCCTACCCTA | 7409 |
rs554332916 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852137 | TCCCTCCTCAGCCTC[C/G]TGAATAGCTGAGACT | 7409 |
rs554388536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6798208 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 7409 |
rs554389226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6846501 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 7409 |
rs554463963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793773 | TAGCATCCAAGATGG[A/G]GCCACTTTGTCTTCA | 7409 |
rs554524904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6788042 | AGATCCCGCCACTGC[A/C]CTCCAGCCTGGGTGA | 7409 |
rs554539230 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800759 | CCAGAGTAGCTGGGA[C/T]TACAGGCGCCTGTCA | 7409 |
rs554557413 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792929 | ACCAAATGTCAACAG[C/T]GCTGAGACCGAGGGA | 7409 |
rs554565555 | snp | C/T | 0.000186619 | 0.00965789 | intron-variant | VAV1 | GRCh38.p7 | 19:6825449 | TCTGGGGTCACTCTG[C/T]CTTGCCTAGGCTGGG | 7409 |
rs554678595 | snp | C/T | 0.000319432 | 0.0126338 | intron-variant | VAV1 | GRCh38.p7 | 19:6833335 | CTTGGTCATCAGTTC[C/T]TTGCTAGAGAAGATG | 7409 |
rs554679100 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817813 | TCTCTCAGCCTCCCG[A/C]GTAGCTGGGACTACA | 7409 |
rs554685548 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6782843 | GCTATAGATCGCGCC[A/G]CTGCAGTCCAGCCCG | 7409 |
rs554761489 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821263 | AAAATTAGCTGGGTG[G/T]GGTGGCCGGCGCCTG | 7409 |
rs554777349 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804289 | AATTCAAGGGTGATT[C/G]CAGTGGTAGGGTAGA | 7409 |
rs554784987 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6810620 | TGAGGCTGGAGAATT[C/G]CTTGAACCCAGGAGG | 7409 |
rs554800442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6826519 | ACTCAGGTTTCTTCT[C/T]CAGCGGGGAAGAGCA | 7409 |
rs554803143 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839552 | GGATTACAGGCGTGA[C/G]CCACCACGCCCGGCT | 7409 |
rs554807786 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844480 | CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG | 7409 |
rs554820649 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804818 | AAGCTCTGCCTCCCA[C/G]GTTCACGCCATTCTC | 7409 |
rs554827371 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831468 | AGGTGCCCGCCACCA[C/G]GCCCAGCTAATTTTT | 7409 |
rs554850899 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824001 | GGAGTGCAGTGGCAC[G/T]ATCATAGTTCACTGC | 7409 |
rs554872169 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811695 | GTAAGAATCGGCAAG[A/G]GAAGCTGGAATGGAG | 7409 |
rs554987233 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794719 | TGGTGTTGGCACCAT[A/C]ATATATTTAGGTTAT | 7409 |
rs554993029 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6800305 | TCTTCTTTGCTTCAC[C/T]ATCTGTCTCATTTTT | 7409 |
rs555056955 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789991 | CGGGTGGATCTCCAA[C/T]ATGGTGAAACCCCAT | 7409 |
rs555076142 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6798186 | GGAGGTGGAGGCAGG[A/G]GAATCGCTTGAACCT | 7409 |
rs555122283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795165 | CAAGAAGCCATACCC[C/T]GGCTTCTCTCTTCCT | 7409 |
rs555131226 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841165 | AGAGACCCACCCTCC[A/T]TGGCTTCCCAAAGTG | 7409 |
rs555208215 | snp | A/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771516 | TCCCAGCACTTTGGG[A/T]GGCTGAGGCGGGCGG | 7409 |
rs555252319 | in-del | -/TTTTTTTTTTTTTTTTTTTTTTTTTTTTT | 0.36606 | 0.221428 | intron-variant | VAV1 | GRCh38.p7 | 19:6844064 | TTCTTCTTCTTCTTC[lengthTooLong]TTTTTTTTTTTTGCA | 7409 |
rs555260894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805151 | GTGGTAAGGCCGGGC[A/G]CAGCGGTTCATGCCT | 7409 |
rs555269354 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848528 | CTGCCTCAGACCCCC[A/G]AGTAGCTGGGATTAC | 7409 |
rs555291485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845347 | CCGAGATTGCGCCAT[G/T]GCACTCCAGCCTGGG | 7409 |
rs555299749 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806527 | TGTGATGGATTCCTT[C/T]TCTGGCTTTGTAAAT | 7409 |
rs555326276 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6847543 | AAGAATATTGTATTA[A/G]AATACTGTTTGTTTT | 7409 |
rs555332701 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824337 | GTCCATGGCAACCAC[A/G]AGCTTACTCGCTGTC | 7409 |
rs555347811 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6778784 | GTGGTGGCTCGTGCC[C/T]GTAATCCCAGCACTT | 7409 |
rs555357673 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817572 | GCCCTCCCCTCTTCA[A/C]ACTGACATTTTATTT | 7409 |
rs555386220 | in-del | -/ATTT | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6834592 | ATTAAATATATAATA[-/ATTT]ATTATTTAATAATAT | 7409 |
rs555402272 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793291 | GTGAGCCGAGATCGC[A/G]CCACTGCACTCCAGC | 7409 |
rs555445597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818234 | GTGGCTAGAGGAGGT[C/T]TCACAGAGAAGGTGT | 7409 |
rs555446790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801353 | GCTCCCTCAACTTGC[C/T]GGGCTGGTCTGGGAG | 7409 |
rs555447229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812347 | AAGCTGATTAATATC[C/T]GAGGTATTTTCCAGT | 7409 |
rs555463510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834028 | ACCCAGGGACAGATC[C/T]CCATAATCATATTAA | 7409 |
rs555486952 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840715 | GCTTAAGTGATCCTC[C/T]CACTTCAGCCTCCTG | 7409 |
rs555511517 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6832499 | CCTCCTCCTCTTTCT[-/C]CTTCTCCTTTCCTCC | 7409 |
rs555524705 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790573 | GCCCCTAGATTGGGG[C/T]TTAGCCCTGGAGGGT | 7409 |
rs555533880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783949 | ATGCAGGTATGGAGC[A/G]GGTTTCAGGAATGCA | 7409 |
rs555547901 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814995 | ATGTTGAGTTGCTAC[C/T]GCATCTTTCATGTGT | 7409 |
rs555671030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778217 | GTTAGGATTGCAGGC[A/G]TTAAGCCACCACGCC | 7409 |
rs555681523 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6811861 | GTACACAAAACAGTA[C/T]AATGCATGTGCTTCT | 7409 |
rs555738959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817932 | ACCTCGTGATCCGCC[C/T]GCCTCGGCCTCCCAA | 7409 |
rs555791439 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854981 | AGAGGTAGAGCTGGG[A/T]CTAAACCACTGTGCT | 7409 |
rs555839146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805352 | ATCGCTTGAACCCGG[G/T]AGGTGGAGGTTGCAG | 7409 |
rs555863551 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775782 | TTTCTGGGTGCCTAA[C/G]TGTCCACAGATTGAA | 7409 |
rs555901932 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855545 | CTCACGCATCTATCT[A/G]ACCATCTATCCACCT | 7409 |
rs555984762 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6785476 | AGCTGGGATTACAGG[C/T]ATGTGCCACCATGCC | 7409 |
rs556019739 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822718 | ATATATATATTAAAA[A/T]ATATATATAAAATAT | 7409 |
rs556020716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6828017 | CTATCTGCACCCACC[C/T]TGCAACTGGCTGTTT | 7409 |
rs556077450 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6811684 | ATATAATTACTGTAA[G/T]AATCGGCAAGAGAAG | 7409 |
rs556111803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6853329 | GGAGTGCAGTGGTGC[A/G]ATCTTAGCTCCCTGC | 7409 |
rs556144151 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | VAV1 | GRCh38.p7 | 19:6822104 | ACATGGCCTGCCCTT[C/G]GAGTCTGAGGTCCCA | 7409 |
rs556171688 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | VAV1 | GRCh38.p7 | 19:6845715 | ATATTATATTATACC[A/G]TACACAATATATTAT | 7409 |
rs556196494 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803253 | AGTAATCAGGGTTGC[A/C]GTCATCTTTGTACCC | 7409 |
rs556233055 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816968 | GACTCCATCTCAAAA[G/T]GGTATAAACACTGAC | 7409 |
rs556244939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840033 | TGAGTGGCATTAAGT[A/G]CATTCACAGTGTTTT | 7409 |
rs556251758 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772677 | CACCCCCTCTCAGGG[C/T]GACAGTTACAGGCAA | 7409 |
rs556252256 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | VAV1 | GRCh38.p7 | 19:6822577 | GGCCGGCAGGTGCAC[C/G]TCCACCTGTCCGGCC | 7409 |
rs556325992 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801272 | CAAACATTGGGTCAA[C/G]TATTTTCATTCCCGA | 7409 |
rs556338095 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798232 | CAGTGAGCGGAGATC[G/T]CATCATTGCACTCCA | 7409 |
rs556360632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812553 | TAATCCCAGCTGTTC[A/G]AGAGGCTGAGGCACT | 7409 |
rs556417571 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785336 | CCACTTCACCTTTTT[C/G]TTTTTTCTTTGTTTT | 7409 |
rs556473322 | snp | C/G | 0.108048 | 0.20579 | intron-variant | VAV1 | GRCh38.p7 | 19:6816518 | TCTCACACGCACACA[C/G]ACACATACGCACACA | 7409 |
rs556477204 | in-del | -/G | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6831140 | TAGGTGAGGGTGGGA[-/G]GGGGAGCTATCTTAC | 7409 |
rs556519369 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784693 | GAGACGGGGTTTCAC[C/T]ATGTTGGCCAAGCTG | 7409 |
rs556602850 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790050 | GGCCATGGTGGCAGG[C/T]GCCTGTAATCCCAGC | 7409 |
rs556665094 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6773278 | TAGGGGTTAACTCTC[G/T]CAAGCCCCAGGCGCC | 7409 |
rs556666012 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816423 | TCCCAGGAGGTGAAG[G/T]CTGCAGTGAGCTATG | 7409 |
rs556666936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779617 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 7409 |
rs556673757 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804483 | GTGCAGTAGTGCAAT[C/T]TCAGCTCATTGCAAC | 7409 |
rs556690448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813540 | GGCTACTACAAACAC[A/G]TTGTCTTAATTACTG | 7409 |
rs556728252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778961 | AGCTCACTGCAGCCT[C/T]GAACTCCTGTACTCA | 7409 |
rs556728898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802627 | CAGACACAGCCATCT[A/G]CTCTATTGTCTCTGG | 7409 |
rs556780264 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813081 | AAACTTAATTGTATA[A/G]AACAACCATTTATTA | 7409 |
rs556788409 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6841942 | TGAAAGTGAGCACTT[C/T]CGGCCGGGCGCGGTG | 7409 |
rs556842495 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824914 | GAATAATTTCACTGT[A/G]AACATTCTTGTACAA | 7409 |
rs556878616 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797531 | CAGTATAGTAAAACC[A/C]AGTCTCTACTAAAAC | 7409 |
rs556945895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775674 | CCTTTGAAGCCCGGC[C/T]GTGTGTCTGGTATGT | 7409 |
rs556971188 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807398 | ACATGTGGAGTTCAC[A/G]GTAGGGTTTGCACTC | 7409 |
rs556981414 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796824 | CTCCTACAATACCTT[C/G]ATTGTCTTCCTTTGC | 7409 |
rs556990447 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6808003 | TCAAAAAAAAAAAAA[A/G]AAAAAGAAAAGAAAA | 7409 |
rs557024284 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6826260 | GGAGAATCGCTTGAA[C/T]CCGGGAGATGGAGGT | 7409 |
rs557027186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809030 | GGGCTAAAGCGAGCC[A/G]CAAGACCAACCCAGA | 7409 |
rs557031830 | in-del | -/AATAATAATAATAAT | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6780113 | AAGACTCTGTCTTAA[-/AATAATAATAATAAT]AATAATAATAATAAT | 7409 |
rs557049617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850503 | AAGACATTAAGGCTT[C/T]AGAGTAGCAAAGGCC | 7409 |
rs557055613 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792535 | GGAAGGAAGGCAGTA[C/G]AGCATAATGGCTAGC | 7409 |
rs557064450 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809759 | CAAAGGTGATCACTG[C/T]GGTGGCTGCTCTAGG | 7409 |
rs557106834 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848382 | CTCTGTCGCCCTGAC[C/T]TTTCTTTTTTCCCCT | 7409 |
rs557114213 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797634 | TTTGAACCCCGGGGG[C/T]AGAGGTTGTTGTGAG | 7409 |
rs557114384 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797368 | AGTTTGAATTACAAA[C/G]AATACAAATTTATCT | 7409 |
rs557190517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803825 | CCACGTCGGCCTCCC[A/G]AAGTGCTGAGATTAC | 7409 |
rs557195211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856488 | GCACTCTGGGAGGCC[A/G]AGATGGGCAGATCAC | 7409 |
rs557201510 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6774731 | TGAGCCACTGTGCCC[A/G]GCTGCTCCTTCTGTT | 7409 |
rs557201864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773700 | GGGATTTCTGCAGGG[A/G]CCCAGGCTGGAGGGG | 7409 |
rs557234281 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6856099 | GAGGAGTTTGAGACC[C/T]GCCTGGCCAACATGG | 7409 |
rs557271956 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6786376 | CTGAGATGGGAGGAT[C/T]GCTTGAGCCCAGGAG | 7409 |
rs557274133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824198 | CTCCTGCCTTGGCCT[C/T]CCAAAGTGTTGGGAT | 7409 |
rs557367864 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | VAV1 | GRCh38.p7 | 19:6808585 | GCCACCTGTGAATTT[C/T]CTTTGTCCTCAGTTT | 7409 |
rs557388925 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6843956 | TTGAACAATTGCTGG[C/T]GCATCAGCTATTTAA | 7409 |
rs557452943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837270 | TTGATCATTTTTGTG[C/T]AAAGGTCCTTTCCTT | 7409 |
rs557591505 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6818316 | GGTGTATTTGTTTGC[A/G]TGGGTGCCACAACAA | 7409 |
rs557596934 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849824 | TACCACATTTTCTTA[C/T]CCAGTCCACTGTTGA | 7409 |
rs557603277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781179 | AAGTGCTGGGATGAT[A/G]ATCGTGAATCATCGT | 7409 |
rs557671829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847645 | TCATTCTCCTTCCCC[C/T]ACTTCTGTCCGGGTG | 7409 |
rs557718607 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | VAV1 | GRCh38.p7 | 19:6780589 | TTTTTTTTTTTTTTT[G/T]GGGACGGAGTCTCAC | 7409 |
rs557721220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840844 | GAGTGGAATGGTGCA[A/G]TCTCGGCCCACTGCA | 7409 |
rs557733859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773582 | GGATCTGAGCTTCCT[C/T]CCTGCATCCATCTCA | 7409 |
rs557750767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802031 | GGGAGGAACCGTCCT[C/T]ATAATGCCTCTCCTA | 7409 |
rs557752400 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812956 | CAGCCCTTTTTATGC[A/T]TCATATAACTGAATT | 7409 |
rs557777152 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790141 | TGAGATCGTGCAAGT[C/G]CACTCCAGCCTGGGT | 7409 |
rs557777276 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | VAV1 | GRCh38.p7 | 19:6808847 | GGTAGTCTAGGAGGG[-/C]CTCATTCACATATCT | 7409 |
rs557850422 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856020 | TCCCTGCTGGCCAGG[C/T]GTGGTGGCTTATGCC | 7409 |
rs557897224 | in-del | -/ATCC | 0.197491 | 0.244423 | intron-variant | VAV1 | GRCh38.p7 | 19:6776081 | TCCATCCATTTATCC[-/ATCC]ATCCATCCATCCATC | 7409 |
rs557909522 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812443 | GCAGATTACTTGAGG[A/T]AAGGAGTTCAAGACC | 7409 |
rs557917798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854172 | AGACTGGAACTGGGG[A/C]CTGGAGAAGGTGAGG | 7409 |
rs557922223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6778930 | CAGCCAGGCTGGAGT[A/G]CAGTGGTATGATCAC | 7409 |
rs557957795 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808541 | CTTTCTACAATGTCA[A/G]AGACCAGCTCCTCCT | 7409 |
rs557985079 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780033 | GGAGAATGGCATGAA[A/C]CTGGGAGGCGGAGCT | 7409 |
rs558057490 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773128 | AAGGAGAGGGAATAT[G/T]CTTACAGGTCCAGGG | 7409 |
rs558070345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806635 | GGAGAGTAAATCACT[A/G]TCCCAGAAGCTGGAG | 7409 |
rs558071448 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829663 | ATGGACAGGTGGGCA[C/T]GGCCAAGTTGGCCAA | 7409 |
rs558083827 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808049 | CGGGCGCGGTGGCTC[A/T]AGCCTATAATCCCAG | 7409 |
rs558125060 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | VAV1 | GRCh38.p7 | 19:6774255 | GCCTCAGCCTCCCGA[A/G]TAGCTGGGACTACAG | 7409 |
rs558145091 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832722 | CTCTTCCTCTTCTTC[C/G]TTTTCCTCCTCCTCC | 7409 |
rs558168294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849192 | CCATGAATGATCCCA[A/G]CACCCAGGGAGTGAT | 7409 |
rs558171650 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813647 | TGGCTGAGGTTTTCT[A/G]TACAAATCTTAGGAT | 7409 |
rs558193246 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818779 | GTGGCTGTCTACTGA[A/G]ATGAGCCCTTAGAGG | 7409 |
rs558207674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6819650 | GAAGATGGATTTTAA[C/T]CAACTCTACTGACGA | 7409 |
rs558237627 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6842479 | CCTACAAAGCATAAT[G/T]CATGGGCACTGACAG | 7409 |
rs558245128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786983 | AAAATAAAATTTAAC[C/T]AATACACGGTCAGGC | 7409 |
rs558271297 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843869 | AGCTCTTGCGATCCA[C/T]AGTGTCCATCTTCTG | 7409 |
rs558272916 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6846559 | GCGAGGCACTGTCTC[-/A]AAAAAAAATTATATA | 7409 |
rs558291707 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803672 | CAGGTCCAAGCTGTT[C/T]TCCTGCCTCAGCCTC | 7409 |
rs558306398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793212 | GGTGGCGGGTGCCTG[C/T]AGTCCCAGCTACTCC | 7409 |
rs558341162 | snp | C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857389 | TGTCGTTCAGAAGGA[C/G]CTGCTAGGAGAGAGA | 7409 |
rs558361152 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788986 | TCCTGGGAGCTGCCC[C/T]GTGTATTCTAAAATG | 7409 |
rs558368606 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791404 | TCCTTGAGCTAGCTC[C/T]TCATCTCGAGGTCCT | 7409 |
rs558403353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855612 | ACCATCCAGCCAACA[C/T]CTATTCATCCATTTC | 7409 |
rs558429677 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6798095 | CAGCCTAGCCAACAT[A/G]GTGAGACCCTGTCTG | 7409 |
rs558573201 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841561 | CTCACTGCAACCTCC[A/G]CTTCCCAGGTTCAAG | 7409 |
rs558596369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814867 | CTCATTATTAAGTAC[A/G]GTGTTTCGGTCTAGG | 7409 |
rs558607305 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6837135 | TTGGAAAGACACCCC[C/T]GGAGTTGGGGAGGGG | 7409 |
rs558633077 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6787945 | AGCCGGGTGTGGTGA[C/T]GGGCACCTGTAGTCC | 7409 |
rs558745811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6809550 | GGTGGGAGAGGTAAG[C/T]GAGAAAAAAAAGAGT | 7409 |
rs558770340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825997 | GCAGTGAGTCAAGAT[C/T]ATGCCACTGGACTCC | 7409 |
rs558778888 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6838270 | TATTTACCTATCATC[C/T]ATCCATCTATTCGTC | 7409 |
rs558779871 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815210 | CGGAGTGCAGTGGTG[C/T]GATCATAGCTCACTG | 7409 |
rs558809245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832497 | CTCCTCCTCCTCTTT[C/T]TCCTTCTCCTTTCCT | 7409 |
rs558823221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848743 | TTCATATATATGTTT[C/T]TTCTTTTTTTTTAAC | 7409 |
rs558832261 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788028 | CTGGCAGTGAGCCGA[C/G]ATCCCGCCACTGCAC | 7409 |
rs558835111 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809970 | GAGGCCAGGAGTTCA[A/C]AACCAGCCTGGACAA | 7409 |
rs558843688 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830886 | TGAGCCCAGGAGTTT[C/G]AGATCAGCCTGGGCA | 7409 |
rs558978422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799420 | TAATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT | 7409 |
rs558994016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849373 | AGCTCACTGCAAACT[C/T]CACCTCCCAGGTTCA | 7409 |
rs558998368 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784587 | CAGCCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT | 7409 |
rs559017624 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770922 | TTTGGAAGACCAAGG[C/T]GGGCAGATCACTTGA | 7409 |
rs559029676 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855807 | TCCACCCATTCATCT[A/G]TCTATCTATCTATCT | 7409 |
rs559054337 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786182 | AGTGCTTTAGAACAC[C/T]ACCTGGCACATAGTA | 7409 |
rs559172334 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771461 | TCTCAAAAGAAAAAA[A/G]AAGAAGAAAGAAGCC | 7409 |
rs559179210 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830099 | GAGTCTCGCTCTGTC[A/G]CCAGGCCGGAGTGCA | 7409 |
rs559196497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824941 | ACAAGTTTTTGTGTG[A/G]ACGCGCTGCCTCTCT | 7409 |
rs559197991 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6780075 | GAGATCAGGCCACTG[A/C]ACTCCAGCCTGGGCG | 7409 |
rs559217252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810510 | GGAGTTCGAGACCAG[C/T]CTGGCCTACATGGTG | 7409 |
rs559220122 | in-del | -/TTCCTTCCTTCCTTCCT | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6789593 | TTTCTTTTCTTTCCC[-/TTCCTTCCTTCCTTCCT]TCCTTCCTTCCTTCC | 7409 |
rs559248727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6796335 | CCGGGAGATATGGCA[A/G]AATATGGGGTGCTTG | 7409 |
rs559249972 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6852065 | GTGGCCCAGGCTAGA[G/T]TGCAATGTTGTGATC | 7409 |
rs559267727 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829220 | GAGCCTGGGCAAGGT[G/T]GGGGCCAGGCTCCTA | 7409 |
rs559276908 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6779915 | AGGAGATCGAGACCA[G/T]CCTGGCTAACACGGT | 7409 |
rs559279554 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847255 | CGCCGCCATCACTGC[C/T]GTTTAGCTCCAAAAC | 7409 |
rs559295571 | in-del | -/GCATACT | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6780447 | AACCTAGAGGGTACA[-/GCATACT]GCACACCTGGGCTAT | 7409 |
rs559313053 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802104 | GACAAAAAACCAAAC[A/G]CCGCATGTTCTCACT | 7409 |
rs559320641 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807667 | CAGTGAGCTGTAATC[A/G]TGCCACTGCACTCAA | 7409 |
rs559341930 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848848 | GCCCAGGCTGGAGTG[C/T]AGTGGTGAGATCTTA | 7409 |
rs559343087 | in-del | -/TG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831880 | GTGTGTGTGTGTGTG[-/TG]CATGTGCACGCCTGC | 7409 |
rs559370669 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6786160 | TTTTGTCTATTTTAC[A/G]TCCCCCAGTGCTTTA | 7409 |
rs559487432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813808 | CCTGTAATCTCAGCA[C/T]TTTGAGAGCCTGTGG | 7409 |
rs559595869 | in-del | -/CTCT | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6776536 | ATCCATCCATCCATC[-/CTCT]CATCCATCCATCCAT | 7409 |
rs559665525 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6798224 | GGAGGTTGCAGTGAG[C/T]GGAGATCGCATCATT | 7409 |
rs559681887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837403 | GCCTCCATTGCCTGT[A/G]TCCTTGCCCTGCTCC | 7409 |
rs559692527 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791453 | GGTCCTTGAGCTAGC[G/T]CCTTATCCTGGGGTC | 7409 |
rs559800629 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804838 | ACGCCATTCTCCTGC[C/T]TCAGCCTCCCAAGTA | 7409 |
rs559801578 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831065 | CTACAGCTAGGACCA[A/C]AGAGTGAGATCCTGT | 7409 |
rs559838721 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6842748 | CTGAGGTGAGAGGAT[C/T]GCTTGAACCTGGGAG | 7409 |
rs559877544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842145 | TGAGGCAGGAGAATC[A/G]CTGGAACCTGGGAGG | 7409 |
rs559914042 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824517 | GAATAATATTCCATT[A/G]TATGGATGGACCACA | 7409 |
rs559971093 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | VAV1 | GRCh38.p7 | 19:6780028 | AAGCAGGAGAATGGC[A/G]TGAACCTGGGAGGCG | 7409 |
rs559978563 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835821 | GCCAGTTTTTGGATA[A/T]TGTGTATAAAGCTGC | 7409 |
rs559980763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799144 | TGTTTATCCATTCAT[C/T]CCTTGATGGAGGTTT | 7409 |
rs559999653 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6808204 | GTAATCCCAGCTACT[C/T]GAGAGGCTGAAGGAG | 7409 |
rs560014873 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6809474 | ATGAGACCTGGAGAT[A/G]AGAGACAGTAAAATA | 7409 |
rs560033856 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6782352 | TAAATAAATAAATAA[A/G]TAAAAATAAAAATAA | 7409 |
rs560036410 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6807574 | AACAGACCATGGACC[A/G]GTACCAGGAGGCTTG | 7409 |
rs560039020 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6813834 | TGTGGTGGGAGAGTC[A/C]CTTGAGGCCAGGAGT | 7409 |
rs560071057 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781547 | CTGTGATACAATCTC[G/T]GTTCATATCACTTGC | 7409 |
rs560081985 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771189 | GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 7409 |
rs560117320 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6821294 | TAGTCCCAGCTACTC[C/T]GGAGGCTGAGGCAGG | 7409 |
rs560170728 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844445 | TGGTCTCGAACTCCT[C/G]ATCTCAGGTGATCCA | 7409 |
rs560200064 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6775910 | GAATGAGAATTCTTC[C/G]CAGTTTCTGTCATTT | 7409 |
rs560223003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852857 | CTTTCCAAAGAGGCC[A/G]GAAACAGGGCCTGCT | 7409 |
rs560246533 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792371 | AGGAAGGCAAGAATT[-/A]AAAAAAAAAAAGGAA | 7409 |
rs560268866 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777300 | CCAGCAATGACAAGG[G/T]CTGCCAGGCCCTGTT | 7409 |
rs560331429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844969 | TGAGGTGAGTCGGGC[A/G]GTCAGATTCTGTCTT | 7409 |
rs560336192 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840460 | ACAGGCACTTGCCAC[C/T]ACGCCTGGCTAATTT | 7409 |
rs560367102 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781765 | GGTGTGCGCCAAGAT[A/G]CCCAGCTAATTTTTG | 7409 |
rs560393548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6815672 | ATGGCATAATGGTTA[C/T]GCACAGGCTTGGAAG | 7409 |
rs560402546 | snp | A/G | 0.00049425 | 0.0157124 | intron-variant | VAV1 | GRCh38.p7 | 19:6820843 | ACACTTGAAGCCCAA[A/G]GACTGAGTTTCAGTT | 7409 |
rs560457443 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799464 | TGAGCCACCATGCCC[A/G]GCCTATACTTTAAGT | 7409 |
rs560458002 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777536 | ATTGCAGCAGAGACC[C/T]GGGGAAAATTAAGGA | 7409 |
rs560458327 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851326 | TATAGGCATGCACCA[A/T]CATGCCTGGCTAATT | 7409 |
rs560467841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850821 | CCCTCCCTGCACCTC[C/T]GCCTTGGGACCCCCT | 7409 |
rs560484178 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6783466 | TGGCGCCATCACCTC[C/T]ATCCTTTTTTTTTTT | 7409 |
rs560510154 | snp | C/T | 0.0566069 | 0.158427 | intron-variant | VAV1 | GRCh38.p7 | 19:6789593 | TTTTCTTTTCTTTCC[C/T]TCCTTCCTTCCTTCC | 7409 |
rs560551181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794017 | AATTGATAAATGATT[C/T]ATTTACCAATAAACC | 7409 |
rs560557618 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838612 | TTACCTATTTATTAT[C/T]ATTTCTCTCTCATCT | 7409 |
rs560605246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817968 | TGGGATTACAGGCAT[A/G]AGCCACCACGCCCAG | 7409 |
rs560620150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837685 | CTGTGTAGCCTTTAC[C/G]CAGTTTCATCAGTTC | 7409 |
rs560753084 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832590 | CTCCTCCTCGCCCTC[A/C]TCTTCCTCTTCCTCC | 7409 |
rs560793093 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792774 | GGGAGTGACTCTGTC[C/T]TCCCAGGGGACATTT | 7409 |
rs560812531 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777158 | ATCCATCCATCCACT[C/T]ATCCACCCGTCTACT | 7409 |
rs560835463 | in-del | -/ATA | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6802336 | CCTAAAATTTAAAGT[-/ATA]ATAATAATAAAATTA | 7409 |
rs560845488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814661 | TCCTTCCTTCCTTCC[C/T]TCCTTCCTTCCTTTC | 7409 |
rs560866977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775895 | AAGGTGTGCAGGCTG[A/G]AATGAGAATTCTTCC | 7409 |
rs560897521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6856742 | AAAGAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG | 7409 |
rs560936196 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771109 | AGATCATGCCACTGC[A/C]CTCCAGCCTGGGTGA | 7409 |
rs560965390 | snp | G/T | 0.000516119 | 0.0160559 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772788 | GAGGGTGCACGGCCG[G/T]CCCTGGGCAGGCGGT | 7409 |
rs560967753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850022 | TCCAAACTGCTTTCC[A/G]CAGTGGCTGAACCAA | 7409 |
rs561128244 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6775144 | AGAAGGCACTCCCCC[C/G]ACCAACCTAAGCATC | 7409 |
rs561128897 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6831608 | TAAGCCACCGCGCCC[A/G/T]GCTGGCTTCTCTATT | 7409 |
rs561132911 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6838351 | TGTCTATCTATCCAT[A/G]TACCTACCCATCAAT | 7409 |
rs561183144 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856252 | TGGTGAGCTGAGATC[A/G]CGCCACTGCACTCCA | 7409 |
rs561195487 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6810107 | TCAATTGAACCCAAA[A/C]GGTGGAGGCTGCAGT | 7409 |
rs561256008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787220 | TCACTCTGTCACCAA[A/G]GCTGGAGTGCAGTGG | 7409 |
rs561287357 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812310 | TTGGGTTTCTCTCTC[-/T]TGAGTGATGAGTGAA | 7409 |
rs561295262 | snp | A/G | 0.000118855 | 0.00770799 | intron-variant | VAV1 | GRCh38.p7 | 19:6832211 | GCCATGTGAGTCCCC[A/G]TCTTCCTCCCTCTTT | 7409 |
rs561311521 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6788345 | TTGAACATGATTCTT[C/T]TTATTTTATTATTAT | 7409 |
rs561316851 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794961 | AGGCTATGCTCAGTT[C/G]GGGCTATTGACTGGA | 7409 |
rs561362410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816268 | TTCATGATCTGCCCT[C/T]CTCGGCTTCCCAAAA | 7409 |
rs561393819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777164 | CCATCCACTCATCCA[C/T]CCGTCTACTCATCTA | 7409 |
rs561435005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793508 | GCGGCAAGACAGGTA[C/T]CTCTCTGCACCATTA | 7409 |
rs561449825 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784913 | TCACAGCCCTTCCCT[C/G]GTTCCCCACTGCCCT | 7409 |
rs561450575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6789759 | TGTGCCACCATATCC[A/G]GCTAATTTTTGTATT | 7409 |
rs561471663 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819450 | GACATTTCCTATGAA[C/T]AGAATTGTACAATAC | 7409 |
rs561497798 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798458 | CATGGTGAGACCAGC[A/C]TCATCTCTAATAAAT | 7409 |
rs561510643 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840127 | CAGCAACCACCTATT[C/G]CCCTCTCCCAGCCCC | 7409 |
rs561542483 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771624 | GCGGACGCCTGTAGT[C/T]CCAGCTACTCAGGAG | 7409 |
rs561575218 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793957 | AATCATTGGTAAATG[A/C]TTTACCAGTGATACT | 7409 |
rs561576863 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852473 | ACGCCTGTAATCCCA[G/T]CACTTTGGGAGGCCG | 7409 |
rs561655257 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802773 | ATCCAGTGCTGGTAT[C/T]TGGTTCTCCATTCCT | 7409 |
rs561728102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845149 | TCTTTGGGAGGCCGA[A/G]GCGGGTCGATCACTT | 7409 |
rs561747904 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853153 | CTTTGGGGATGCCAT[C/T]GACACCCCTTCCAAT | 7409 |
rs561753089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800616 | CACCCAGCTTCTTTT[C/T]TTTGTTTTGTTTTGT | 7409 |
rs561810660 | snp | C/T | 1.76543e-05 | 0.002971 | intron-variant | VAV1 | GRCh38.p7 | 19:6833518 | TCTTTATGTGTTCCC[C/T]GCATCTCAGAGGTAC | 7409 |
rs561810781 | snp | A/C | 8.91385e-05 | 0.00667542 | missense | VAV1 | GRCh38.p7 | 19:6826697 | GCCCGGGAGGACGTG[A/C]AGATGAAGCTGGAGG | 7409 |
rs561835183 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811313 | AGTGCTGGGATTATA[A/G]GCATCAGCCTCCACA | 7409 |
rs561842297 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839307 | AATCCTCTCATAGAA[C/T]ATCCTTCTCTTTTTT | 7409 |
rs561873497 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810857 | CTGGCAATGATGTCA[A/G]TCTTGGACCTGTTAA | 7409 |
rs561880050 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812243 | ACTAAGGGCTTGGAG[A/G]CAGTAACACTCAGTT | 7409 |
rs561939070 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831621 | CCGGCTGGCTTCTCT[A/G]TTTCTCAACCTGTGT | 7409 |
rs561987829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790075 | CCCAGCTACTCGAGA[A/G]GCTGAGGCAGAAGAA | 7409 |
rs561989006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839672 | GATTATGGCAAAATA[C/T]ATAGAACATAAAAGT | 7409 |
rs562061494 | snp | A/G | | | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6853056 | TCAAGGAGCCTGAAA[A/G]GAGAACCATCAGCAG | 7409 |
rs562095470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854282 | CCTGCATGTATTCAG[C/T]ACCTGCTGTGTGCAG | 7409 |
rs562200021 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811288 | TGATCCACCCTCTTC[A/G]GCCTCCCATAGTGCT | 7409 |
rs562202842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6801740 | CCGTCGTGCTTGGCT[C/T]TGGGTCCCCTTCTCC | 7409 |
rs562219031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6840990 | ACCATGTTGGCCAGG[C/T]TGGTCTCGAACTCCT | 7409 |
rs562255054 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794421 | GAGGCAGGAGGATTG[C/T]TTGAGCCCAGGAGTT | 7409 |
rs562276180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822156 | AAAGCCCTGCGCTGG[A/G]GTCTGCGGGGACCCT | 7409 |
rs562321080 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773039 | CGGGCAGGTGTGCTG[A/G]GGGTTGGAGACGGGG | 7409 |
rs562375740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6853813 | CCCTTACAGTACAGG[A/G]CATCTAATACTCTGC | 7409 |
rs562398199 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6826263 | GAATCGCTTGAACCC[G/T]GGAGATGGAGGTTGC | 7409 |
rs562417313 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6802382 | ACCTCCTGTCCTTTG[C/T]CACTTTCTCACACTC | 7409 |
rs562419952 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778433 | GTGGGGAGAGGGTGG[C/G]ACAGTTAGAGTAGGG | 7409 |
rs562423799 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836307 | ATTCCAGTTTCTCCA[C/T]GTCCTTGTCAACACT | 7409 |
rs562445156 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839246 | TTTTTTAGAGATAGG[G/T]TCTCACTATGTTGTC | 7409 |
rs562484121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832631 | CCACCTCTTCTTCCT[C/T]CTCCTCCCTTTCCTC | 7409 |
rs562548715 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817289 | GGCTGGTTTTGAACT[A/C]CTGACCTCAAGTAAT | 7409 |
rs562640577 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6816167 | TGGGACTACAGGCGC[A/C]CACCACCACGCCCAG | 7409 |
rs562666501 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795624 | TGGCACAGGGTGGCA[C/T]GTCTTAGCTCTACTG | 7409 |
rs562715688 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851499 | CAAATATGTTATAGA[C/T]AGAAACCTAATTAAT | 7409 |
rs562757069 | snp | A/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771606 | AATTAGCCAGACGCG[A/G]TGGCGGACGCCTGTA | 7409 |
rs562779074 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6810706 | GTGAAACGTTATCTC[A/C]AAAAAAAAAAATTAC | 7409 |
rs562782885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844541 | ATCTTCTAAGTGTGT[A/G]CCACATAGTAGCAGG | 7409 |
rs562790167 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6794905 | AGAATGCTCTGGAGG[A/G]TTCTTCGTCACATGA | 7409 |
rs562813737 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6852362 | GTGGCCCCATAGAAG[G/T]TTTTGAATTTGGTGA | 7409 |
rs562816294 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6847739 | AGACACCCAGCCAGA[A/C]CCAAAGGGCTGAGCC | 7409 |
rs562866066 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6778303 | AGGCCAAGAGACTGG[A/T]GAGGAAAGAACAGAT | 7409 |
rs562867063 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811993 | GGGAGAGAGGAGGTA[G/T]GGAGAAGTAATTTCT | 7409 |
rs562979382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806244 | GGTGCATTCCACCAC[A/G]CCCAGCTAATTTTTG | 7409 |
rs563069143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779241 | ATTTTTTGTAGAGAT[A/G]GGGTTTTGCTATGAT | 7409 |
rs563112092 | snp | C/T | 0.000399281 | 0.0141238 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826663 | GTCAGCCAGCAAACA[C/T]CTGGACCGTGTGGCC | 7409 |
rs563123157 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6791411 | GCTAGCTCCTCATCT[C/T]GAGGTCCTTGAGCTA | 7409 |
rs563151790 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829007 | TCTGGGTGGAGCCTG[A/G]GCAGGGGCGGGGCCG | 7409 |
rs563267869 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6822918 | ATGATATTTATAAGA[C/T]ATAAAATATATAGTT | 7409 |
rs563283686 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6852243 | TGGTCTTGAACTCTT[A/G]GCTTCAAGTGAACTT | 7409 |
rs563291582 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6834283 | GAGTCTTGCTGTGTC[A/G/T]CCCAGGCTGGAGTGC | 7409 |
rs563331421 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779137 | GCTCACTGCAGCCTC[A/G]AACTCCTGTGCTCAA | 7409 |
rs563346438 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827849 | AAGTGATCCTCCCGC[C/G]TCGGCCTCCCAAAGT | 7409 |
rs563377139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806791 | TCAGCCCATGTTGCT[A/G]GAAGAGAAAGAGGAA | 7409 |
rs563405230 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817816 | CTCAGCCTCCCGAGT[A/G]GCTGGGACTACAGGC | 7409 |
rs563444541 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795381 | TATCGCTCGCGAAAT[A/T]GGAGCCCTACTTCAT | 7409 |
rs563448821 | in-del | -/CAT | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6776161 | GCTCATCTATCCACC[-/CAT]CCATCCATCCATCCA | 7409 |
rs563559141 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6828315 | TCAGCCTCCAGGGTC[A/G]GCAGTACGATGGAGG | 7409 |
rs563564195 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6802936 | GTCCTCTATTTACCC[A/T]AAGGAGTTGAACATT | 7409 |
rs563658015 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836139 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGACA | 7409 |
rs563670598 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774285 | GGCGCCCGCCACCAC[C/G]CCTGGCTAATTTTTT | 7409 |
rs563683157 | in-del | -/TTTG | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6830049 | ACTCAACAGGTGTTT[-/TTTG]TTTGTTTGTTTGTTT | 7409 |
rs563731830 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830931 | CCGTCTCTACAAAAC[A/T]TAAAAAAAAATTTAG | 7409 |
rs563771214 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808264 | TTGCAGTGAGCCAAG[A/T]TCACACCATTGCACT | 7409 |
rs563840012 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784240 | CCAGACTGGACAAAA[A/C/G]AGTAAGACCCTGTCT | 7409 |
rs563855212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830336 | TGCTGGGATTATAAG[C/T]GTGAGCCCACTCAAC | 7409 |
rs563918047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6847058 | AGCTGGGATTACAGG[C/T]GCCCGCCATCAAGCC | 7409 |
rs563944179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834186 | AGATGAGGTCTTGCT[A/G]CGTTGCCCAGCCATA | 7409 |
rs563945522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842086 | ACAAAATTAGCCGGG[C/T]GTGGTGACACACACC | 7409 |
rs564029837 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790658 | TTATTGAAGCAACCA[C/T]GCAGAGCAGCAGCAG | 7409 |
rs564088686 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6827553 | AGCTAGGATTACAGG[C/T]CTGAGCAATCGTGCC | 7409 |
rs564106076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6839755 | GGAGTGCAATGGTGC[A/G]ATCTTGGCCCACCGC | 7409 |
rs564114672 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6802203 | TGTGGGGTCGGGGAA[A/G]TGGGGAGGGATAACA | 7409 |
rs564137046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811938 | GGCTACTTTCATTTG[C/T]AGTTTTGCCATCCCT | 7409 |
rs564184316 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6839337 | TCTTTTAAAAAATTG[A/G]GGTGAAATTTGCACA | 7409 |
rs564196369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821930 | AGGGTGTGGGGGGAC[A/C]TGGCCTTGCCCTCCG | 7409 |
rs564215104 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792328 | GAAGGGTGGAGGTGG[A/G]TGAAAAGAGGAGGCA | 7409 |
rs564247852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806206 | ATTCTCCTGCTTCAG[C/G]CTCCCGAGTAGCTGG | 7409 |
rs564252463 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6802837 | TCTGAGCCTCAGTTG[A/T]TTCCTCTGTCAAAGG | 7409 |
rs564284733 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6805563 | CCTGGGCAACATAGT[A/G]AGACCCTCATTTCTA | 7409 |
rs564328576 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6852614 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 7409 |
rs564376792 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836056 | TTTCTGTAGTTTTAG[G/T]AGAGATGGGGTTTCA | 7409 |
rs564391539 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6828296 | GGGTCACTGGGGTCA[C/T]GTCTCAGCCTCCAGG | 7409 |
rs564414999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806989 | CAGGTACAACCTGTT[A/G]TAATCAATGCTGTGT | 7409 |
rs564488325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817947 | CGCCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 7409 |
rs564554421 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829433 | GGTAGGGGTGGGGCC[A/T]GGTTCTTATGTAGAC | 7409 |
rs564579492 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773775 | TATATTCAAATCCCT[A/G]TTTGAATGTGGTTGG | 7409 |
rs564610036 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6842016 | GGATCACCTGAGCTC[A/G]GGAGTTTGAGACCAG | 7409 |
rs564642237 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835048 | ATCCTGTTTCAAAAA[A/C]ATAAAAAAATAAATA | 7409 |
rs564689630 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814607 | CTTCTTCTGCAAAAA[A/T]GACTTTCTTTCTTTC | 7409 |
rs564700411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854332 | GGAGACAGAAACAAG[C/T]ACGGTACAAGGATTG | 7409 |
rs564702697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817757 | AGTGGCACCGTCGTG[C/G]CTCACCGCAGCCTCC | 7409 |
rs564771064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847818 | GAAGCCCGCTCCCCA[C/T]GTCTGGGCTCCGGCC | 7409 |
rs564821170 | in-del | -/TC | 0.0688775 | 0.172321 | intron-variant | VAV1 | GRCh38.p7 | 19:6843116 | TACACTAAGTTGGGG[-/TC]TCTCTCTGTATTCTT | 7409 |
rs564827435 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6818426 | CTCTTCTTCCTCCTC[A/G]CCCACTCTAACTCCA | 7409 |
rs564844181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775062 | TGAGCCACCATGCCC[A/G]GCCCTTCTGTTTCTT | 7409 |
rs564861670 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6823941 | TGTTTCTTTTTTTTT[G/T]ATTTGTTTTGTTTTG | 7409 |
rs564931507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855868 | TATCTATCTACCTAT[C/T]TATCCACCTACCCAT | 7409 |
rs564945310 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6830216 | GGCACACACCACCAC[A/G]CCCAGCTAATCTTTG | 7409 |
rs565159508 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844718 | CGTTAGCGCTCCTTC[C/T]GCCCTTCTGCGCCGA | 7409 |
rs565181244 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786196 | CCACCTGGCACATAG[G/T]ACGGAATCAATTAAT | 7409 |
rs565278148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837512 | TGACTTCAGATCTCT[C/T]CCTCTCTCCCCAACC | 7409 |
rs565390152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831548 | CAAACTCCTGACCTC[A/G]TGATCCGCCCACCTC | 7409 |
rs565403272 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6825541 | TGGGCGAGGGGCTGC[C/T]CATCTCTGGTTCAAT | 7409 |
rs565408277 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6819416 | TTGATCTTGGACTTC[C/T]AGTCTCAGAACTATC | 7409 |
rs565451712 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6797761 | AAAAAAAAAAAAAAA[A/G]AGAGTAGGAGCAAAA | 7409 |
rs565452183 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6836899 | GATGGGGCAGGATCC[A/T]CGTGTAGGGTTATGG | 7409 |
rs565483335 | in-del | -/TCCTCCTCCTCTTTCTCCTTCTCCTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832483 | TGGTTTCCTTCCTCC[-/TCCTCCTCCTCTTTCTCCTTCTCCTT]TCCTCCTCCTCTTTC | 7409 |
rs565514449 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6791119 | TGGATTTAGGGCCCA[A/C]CTGGATGATCCCAGA | 7409 |
rs565515356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773535 | GCCTGGGCCTGGGGC[A/G]GCATGGGGCAGGTGG | 7409 |
rs565518177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803577 | GAATATTATTATTAT[C/T]ATTAGAGATGGACTT | 7409 |
rs565542270 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804885 | CCCGCCACCATGCCC[A/G]GCTAATTTTTTGTAT | 7409 |
rs565577560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779348 | ATGAGCCACTGCACC[C/T]GGCCAGAATAGAGGT | 7409 |
rs565578145 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | VAV1 | GRCh38.p7 | 19:6819385 | GTGTTTTGAAGAAAC[C/G]AACCCTACTGACACC | 7409 |
rs565589090 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6798362 | GCAGGGCATGGTGCC[C/T]GAAGCCTGTAATCTC | 7409 |
rs565632945 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844941 | AATAGAGCTGGGAGT[A/C]AGAGGAGGTGGGTGA | 7409 |
rs565659436 | snp | G/T | 1.7107e-05 | 0.00292459 | intron-variant | VAV1 | GRCh38.p7 | 19:6854150 | GGGGTTGAGCTGGTG[G/T]TGGACGAGACTGGAA | 7409 |
rs565693707 | in-del | -/C | 0.411746 | 0.190626 | intron-variant | VAV1 | GRCh38.p7 | 19:6780067 | GTGAGCCGAGATCAG[-/C]GCCACTGCACTCCAG | 7409 |
rs565779000 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6807789 | TGAGGTCAGGAGTTC[A/G]AGACTAGTCTGACCA | 7409 |
rs565816059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807428 | CCTATGAGGATCTAA[C/T]GCTGCAGCTGATCTG | 7409 |
rs565817954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813357 | AAAATGGAGCTTCGA[C/T]ATGTTTCATTATTTA | 7409 |
rs565851959 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822027 | CCTGCCCTGGGGTCT[G/T]GGGGGACATGGCACT | 7409 |
rs566019939 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799991 | TATGATAGGTGCATG[A/C]TTAATGTTTTAAGAA | 7409 |
rs566020867 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6791712 | ACAAATAGACAAAAC[A/G]CTGGCACATTGTAAT | 7409 |
rs566023374 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819794 | CTTCAGGATCTGGGG[A/G]ACCTCAGAGAGTGCT | 7409 |
rs566030369 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814073 | TCTAAAAATAAATCA[A/G]TGAATGAATAAATAA | 7409 |
rs566046886 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6780587 | TCTTTTTTTTTTTTT[G/T]TTGGGACGGAGTCTC | 7409 |
rs566111019 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831343 | TTTGAGACGGAGCCT[A/C]GCTCTGTCACCAGGC | 7409 |
rs566185948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825226 | TTGAGCGGCATGGGG[C/T]GGGTGGATGACCCTT | 7409 |
rs566225823 | in-del | -/ATTACAGGC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841186 | TCCCAAAGTGCTAGG[-/ATTACAGGC]ATGAGCCACCGTGCT | 7409 |
rs566274238 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6831733 | CACATCCTATTCACT[G/T]CTCTGTCCCCAGCTC | 7409 |
rs566296165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793089 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCGAGG | 7409 |
rs566302507 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | VAV1 | GRCh38.p7 | 19:6832570 | TCCTCTCCTTCCTCC[C/T]CTTCCTCCTCCTCGC | 7409 |
rs566328175 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6823525 | ATATTTTATATATAT[A/T]TTTTGTTATGTTAAC | 7409 |
rs566331340 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808496 | CTTATGCAATAATCT[G/T]AGCTTAATCAGTCCA | 7409 |
rs566379549 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806383 | AGCCACCATGCACGG[A/C]CAACAATTTTTTTTA | 7409 |
rs566406180 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836232 | TAGATACAATGTTTA[A/G]CTTCAGTAGATATTG | 7409 |
rs566417859 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829648 | GTGGGTGAAGTCAGG[A/C/T]TGGACAGGTGGGCAT | 7409 |
rs566466035 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808851 | GTCTAGGAGGGCCTC[A/T]TTCACATATCTGCTG | 7409 |
rs566517713 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6844807 | AGATTTAAGGGGACG[A/C]TGAAAATCTCAGTCA | 7409 |
rs566525205 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6852496 | GGAGGCCGAGGCAGG[C/T]GGATCACGAGGTCAG | 7409 |
rs566555708 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774889 | CCTCCCAAGTAGCTG[C/T]GACTACAGGCACACA | 7409 |
rs566563400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851865 | AATGGATCCTTGACT[C/T]CCCCAAAGTTTAATT | 7409 |
rs566592219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774533 | TTAGCCTCTCAGGAT[C/T]AAGCAATTCTCCTGC | 7409 |
rs566628216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845216 | TGAAACCCTGTCTCT[A/C]CTAAAAATACAAAAA | 7409 |
rs566657589 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842968 | GGCAGTCTCTCCCCC[A/G]AGGTTCTGGGACTTT | 7409 |
rs566682177 | snp | C/T | 0.029116 | 0.117091 | intron-variant | VAV1 | GRCh38.p7 | 19:6814690 | TCTTTCTTTCTTTCT[C/T]TCTTTCTTTCTTTCT | 7409 |
rs566696413 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780971 | TGGAGTGCATTGGCA[C/T]GATCTCTGCTCACTG | 7409 |
rs566705826 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856368 | CAGACAAAAAGCTTG[G/T]AAATAAGCAAATGAT | 7409 |
rs566707687 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849632 | TTATTCCCATCTTTA[G/T]GTCCATGTGTACCCA | 7409 |
rs566716503 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810962 | GGCATGCTTTCAACT[C/G]TTGTTCCAAAACCTT | 7409 |
rs566725770 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6843724 | GTCTGTCAAGTGCTT[A/G]GTCCTGGTCCTGACA | 7409 |
rs566745058 | in-del | -/GTAGAGACAGG | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6840959 | ATTTTTGTATTTTTA[-/GTAGAGACAGG]GTTTCACCATGTTGG | 7409 |
rs566805469 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797567 | AATTAGCTGGGCGTG[C/G]TGACGCATGCCTGTA | 7409 |
rs566836432 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6804777 | CGCACAGGCTGGAGT[G/T]CAGTGGCGCAATCTT | 7409 |
rs566890478 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834143 | GGTGCACACCACCAC[A/G]CCTAGCTAATTTTTT | 7409 |
rs566913542 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | VAV1 | GRCh38.p7 | 19:6857290 | TAATTTATAACACCC[C/T]GATTTCCTCTTGGGT | 7409 |
rs567028730 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6830745 | GTGCCCAGCTTATTT[G/T]ATTTCTTGTATGGTA | 7409 |
rs567030707 | snp | C/T | 8.23716e-05 | 0.00641709 | intron-variant | VAV1 | GRCh38.p7 | 19:6836959 | TATAACCTCTCTGTT[C/T]CTGTTTTTGTCTCCT | 7409 |
rs567034083 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6788491 | AATTCTTGTGCCTCA[A/G]CCTCCCTAGTAGCTG | 7409 |
rs567057006 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6776479 | CCATCCATCCATCCA[C/T]TCATCCATTCATCCA | 7409 |
rs567077496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6815367 | GGCTGGTCCCAAACC[C/T]CTGACCTCAAAGTGA | 7409 |
rs567143781 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | VAV1 | GRCh38.p7 | 19:6815938 | TCCCACCCGTAATAC[C/G]AACATTTAGGGAGGC | 7409 |
rs567168402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6803177 | AGTGAAAGTGCATAG[C/T]GGCAGTTGCAGAAGT | 7409 |
rs567180420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6820108 | CAGATTCCTCAAGTC[C/T]AGGAATTCAAGACCA | 7409 |
rs567182829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842232 | CAAAACTCTGTCTCA[A/G]AAAGAACAAATAAAT | 7409 |
rs567337634 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782141 | TCAAGACCAGCCTGT[C/T]CAACATGGCGAAAGC | 7409 |
rs567360971 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792556 | AATGGCTAGCACATG[G/T]TTCTTTTTTCTGTTT | 7409 |
rs567361334 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6797965 | AACCAGCTATATTGA[C/T]ATACAGTAAATTACA | 7409 |
rs567382288 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771426 | TGCACTCTAGCCTGG[G/T]CAACGAGAGTGAAAC | 7409 |
rs567395925 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778049 | TCAAGCGATTCTCCT[A/G]TCTCAGCCTCCTGAG | 7409 |
rs567409859 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848951 | GGTGTGCACCACCAC[A/T]TCCAGCTAATGTTTA | 7409 |
rs567424553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6855897 | ATCAATCCAATAATC[C/T]ATCCATTCATCTATC | 7409 |
rs567439445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851687 | TGCTTCTGTTTGGTG[C/T]CTTGTAATTTTCAAC | 7409 |
rs567440411 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6780501 | TCCTAGCTACAAACC[C/G]GTACAGCATGGGACT | 7409 |
rs567443407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6776799 | GTCTCACTCTGTCAC[C/T]CAGGCTGGAGTGCAG | 7409 |
rs567505661 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6851037 | ATATGTATGTGTGTA[C/T]ATATGCATATATACA | 7409 |
rs567639637 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856563 | CCCGTCTCTACTAAA[A/T]ATACAAAAAAATTAG | 7409 |
rs567691544 | in-del | -/A | 0.171704 | 0.237423 | intron-variant | VAV1 | GRCh38.p7 | 19:6797939 | GTATCCTGCTGACTT[-/A]AAAAAAAAAAAACCA | 7409 |
rs567740930 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6824720 | TAGTTTTAGTAGAGA[C/T]GGGGTTTCACCATCT | 7409 |
rs567758626 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6810453 | TCATGCCTTTAATCC[C/G]AGCACTTTGAGAGGC | 7409 |
rs567854730 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799565 | CCATCAACCCATCAT[C/G]TACATTAGGTATTTC | 7409 |
rs567866698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781181 | GTGCTGGGATGATAA[C/T]CGTGAATCATCGTGC | 7409 |
rs567913292 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6819021 | CTCAGGAGGCTGAGA[C/T]AGGAGAATTGCTTGA | 7409 |
rs567931076 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6782857 | CGCTGCAGTCCAGCC[C/T]GGGTGACAGAGTGAG | 7409 |
rs567952570 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787865 | GTGGATCACGAGGTC[A/G]GGAGATCGAGACCAT | 7409 |
rs568005236 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6794095 | TTACCAATAAACCAA[C/T]GGTAAATGATTTATT | 7409 |
rs568014219 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848327 | ATAGAGGCTCAAAAA[A/G]GCTCTTAAAATTAAT | 7409 |
rs568025105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821408 | TCCGTTAAAAAAAAT[A/G]CTAAAATATAAAAGA | 7409 |
rs568093740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6833386 | AATTGGGAGATGGGG[A/G]AGTCCCTACTTTGAT | 7409 |
rs568124590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806312 | GGCTGGTCTCGAACT[C/G]CTGACCTTGTGATTC | 7409 |
rs568187092 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6827799 | GAGACGGGGTTTCCC[C/T]GTGTTGGCCAGGCTG | 7409 |
rs568188165 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807242 | AATGAAATAAGTATA[C/T]AACTCACCATAATGT | 7409 |
rs568196278 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821009 | CACTTGCTGTGTGAC[C/T]TTGGATACGTGGCTG | 7409 |
rs568223906 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844066 | CTTCTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 7409 |
rs568236313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6825938 | GCATGCACCTGTAAT[C/T]CCAGTTACTCAGGAG | 7409 |
rs568236456 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824438 | GCTTCTTTTGCTGAG[C/T]GTAGTGTTTTCAAGG | 7409 |
rs568254522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804764 | AGTCTTGCTCTGTCG[C/T]ACAGGCTGGAGTGCA | 7409 |
rs568255569 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6838661 | CATCACCTGTCTGTT[A/T]ATCATCTATCATCTT | 7409 |
rs568256814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6799798 | TGCAGTGAGCTGTGA[C/T]TGGGCCAGGCTGCAC | 7409 |
rs568315961 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801187 | GGCATACAGTAGGCA[G/T]TCCACACATGCTTGC | 7409 |
rs568332593 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832577 | CTTCCTCCCCTTCCT[C/G]CTCCTCGCCCTCCTC | 7409 |
rs568333106 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | VAV1 | GRCh38.p7 | 19:6832674 | CTCCTCCTCCTCTTC[C/T]TCCTCTTCTTTCTCT | 7409 |
rs568338687 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811130 | AGCCTCCGCCTTCCA[C/G]GTTCAAGTGATCCTC | 7409 |
rs568411854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805681 | CATTACATTTATTGT[C/T]CACTTTATTTCTATT | 7409 |
rs568450609 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6811571 | TTTCCTGGAAGAAGA[C/G]ATATTGGAGATGGGC | 7409 |
rs568457652 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6800767 | GCTGGGATTACAGGC[A/G]CCTGTCACCACGCCT | 7409 |
rs568484706 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6785949 | CAGGTAATGAGCCAC[C/T]GCGCCCAGCCCAGAT | 7409 |
rs568501268 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841138 | CAGGCTGGTCTCGAA[A/C]TCCTGGGCTCAAGAG | 7409 |
rs568538428 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | VAV1 | GRCh38.p7 | 19:6778074 | CCTGAGTAGCTGGGG[C/T]TACAGATGCGTGCCA | 7409 |
rs568553011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845376 | GGCAACAGAGCGAGA[C/T]TCGGTCTCAAAAAAT | 7409 |
rs568571655 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6820140 | CCTGGGCAACATAGC[A/G]AGACCTCGTCTCTAC | 7409 |
rs568585187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816845 | GGCACACTCCTGTAG[G/T]TCCAGCTACTTGGGA | 7409 |
rs568629244 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792382 | GAATTAAAAAAAAAA[A/G]GGAATGAAATGAAAT | 7409 |
rs568629334 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6847303 | GAGAAACCCCATCCC[A/G]GGCAGTTGCTCCTGC | 7409 |
rs568648754 | in-del | -/AAC | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6852721 | CCAGACTCCGTCTCA[-/AAC]AAGAAAAAAAAAAAA | 7409 |
rs568664971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6853172 | ACCCCTTCCAATGGC[C/T]TTGCAGAGGTCATAT | 7409 |
rs568677544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804205 | ACGCACGGCAGGCAA[A/G]CCCCAAAGTGGGGCT | 7409 |
rs568677916 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6777497 | GGGGGGCACTTTGAC[A/G]AGGAGGGCTAGTGGT | 7409 |
rs568695091 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6805156 | AAGGCCGGGCGCAGC[A/G]GTTCATGCCTGTAAT | 7409 |
rs568703028 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813035 | CCTTTATCCTTGTTA[C/T]CTATTTATTGCTAAG | 7409 |
rs568704277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839912 | GCCCAGGCTGGTTTC[A/G]AACTTCTGGGCCCAA | 7409 |
rs568708627 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797613 | GAGGCTGAGGCAGGA[A/G]AATTGTTTGAACCCC | 7409 |
rs568711072 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853919 | ATCTGCCCCAGACCC[A/T]TTTCTCACTTCTGTT | 7409 |
rs568716736 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6803814 | AGGTGATCCAGCCAC[A/G]TCGGCCTCCCAAAGT | 7409 |
rs568745219 | snp | C/T | 0.000165557 | 0.00909677 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825329 | TGTTCATACTCACTT[C/T]CTAAAGGAGATGAAG | 7409 |
rs568751254 | in-del | -/GAAG | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771824 | AAGGAAGGAAGGAAG[-/GAAG]AAAGGAAGGGAGGGA | 7409 |
rs568784176 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775292 | AGTCAAGCTCTCTGT[C/G]ATGCTTCAATAGCAG | 7409 |
rs568793978 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6793724 | TCAGGAGACATTCCC[A/G]GGAGTGGGGTTAATC | 7409 |
rs568805913 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6794036 | TACCAATAAACCAAC[A/G]GTAAATGATTTATTT | 7409 |
rs568820218 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6832314 | GACCACTCTGAACCA[C/G]AGTCTCTTCATTTGG | 7409 |
rs568821811 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827015 | GATTGTACCCCAAGT[C/T]GGGCTGAGCTCCCAC | 7409 |
rs568877691 | in-del | -/AAAAAAA | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771164 | AAAAAAAAAAAAAAA[-/AAAAAAA]GCCGGGCGCGGTGGC | 7409 |
rs568884770 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830450 | TTTGTTTGTTTGTTG[C/G]TTTGTTTTTGAGACA | 7409 |
rs568941502 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6788508 | CTCCCTAGTAGCTGG[G/T]ATTACAGACAGGTAG | 7409 |
rs568956573 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823917 | CATTTGTTTTGTTTT[G/T]GTTTTTTTTGTTTCT | 7409 |
rs569020742 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839865 | CTGGCTAATTTTTTG[C/T]ATTTTTCGTAGCGAT | 7409 |
rs569029955 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831849 | GTGTGCTTCTGCAAA[A/G]GGGAGTGTGTGTGTG | 7409 |
rs569108613 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | VAV1 | GRCh38.p7 | 19:6843195 | TTTATTTTTGTTTCA[A/G]TGAGAGGTTTCTGGG | 7409 |
rs569128815 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6815995 | AGCCTCGGCAACATA[A/G]TGAAACTCTCTGTCT | 7409 |
rs569132742 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836177 | CCGTGCCCAGCCAGG[A/T]CACATGTTTTCATTT | 7409 |
rs569186531 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6837934 | GTATTTAAATGTTGT[C/T]AATTTCCCCAAAAAT | 7409 |
rs569232020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800206 | TGCAAGGTAAAAAAA[C/T]AATAGTAATAACAAG | 7409 |
rs569232136 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6798666 | CTCCCCTTCCCCCCC[-/G]CCACCCAAAAGAAGG | 7409 |
rs569239862 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6805086 | TATGCAGAAATTTCC[A/G]GGGAAGGGGTAGTAA | 7409 |
rs569297178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778701 | ACTGCATTCCAGCCT[A/G]GGCAACAGAGAGAGA | 7409 |
rs569306083 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6852104 | CTGTGGCTTCAAACC[C/T]CTGGGCTCAGGCGAT | 7409 |
rs569359967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6778189 | TGACCCACATGCCTC[A/G]GCCTCCCAAAGTGTT | 7409 |
rs569436559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773095 | GGGCTGACGTGCTGC[C/T]CCACCTCTGGGCCTG | 7409 |
rs569462970 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845118 | GGGCGCAGTGGCTCA[C/T]GCCTGTAATCTCAGC | 7409 |
rs569474521 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771483 | AAAGAAGCCTGGCGC[A/G]GTGGCTCACGCCTGT | 7409 |
rs569491622 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771772 | AGAAAGAAACAAAGA[C/G]AGAAAGAAAGGAAAG | 7409 |
rs569595387 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6784442 | GGCCAACAGGAGGGG[C/G]ATCTAGGAGGGTCAG | 7409 |
rs569690762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817522 | ACACATAAGGTACTA[C/T]CATAGTTGCTGGGCA | 7409 |
rs569748379 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6796571 | TTTGCACTAACCTCA[A/G]GGCTTCTTGTACTAA | 7409 |
rs569753294 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6847408 | ATGGAAATCACACAG[C/T]GTGTGGCCGTTTGTG | 7409 |
rs569763725 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6812869 | AAGAATGGTGATGAG[A/G]AGAATGGTGATGGTG | 7409 |
rs569772534 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818025 | GATCTCATTATGTGG[C/T]CCCAGGCTGATTTTG | 7409 |
rs569798738 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6812212 | GCCTCTGCCCGAGGT[A/G]GACAGCAGGAATAGA | 7409 |
rs569809435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6821945 | ATGGCCTTGCCCTCC[A/G]GGAAATAAGGTCATA | 7409 |
rs569817033 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6779823 | TAGCTTCTAAAAAAT[-/A]ATAAAAGGCCGGGCA | 7409 |
rs569818843 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6826898 | AACAGAAATGGGCTG[G/T]CCCTGGGTCTGGGCT | 7409 |
rs569853799 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844521 | CTCGCCCAGCCGACG[A/C]TCCCATCTTCTAAGT | 7409 |
rs569877197 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6826802 | TTGCAGATGGTCCAC[-/T]TTCTGCTGCAGCCCA | 7409 |
rs569925302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816972 | CCATCTCAAAAGGGT[A/G]TAAACACTGACAGTG | 7409 |
rs569934422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801280 | GGGTCAAGTATTTTC[A/G]TTCCCGACGTACAGA | 7409 |
rs569973215 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803778 | CCATGTTGGCCAGGC[G/T]GGCCTCAAACTCCTG | 7409 |
rs569979381 | snp | C/T | 6.59826e-05 | 0.00574343 | intron-variant | VAV1 | GRCh38.p7 | 19:6821574 | GAAGCTGTGTTCTGC[C/T]GTGGGGGTGTACAAG | 7409 |
rs570028456 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810883 | GTTAAGTTTGAGGTG[C/T]CCATTGTTGAAAGAA | 7409 |
rs570060962 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6785905 | TTCAAGTGATCCGCC[C/T]GTCTCGGCCTCCCAA | 7409 |
rs570159450 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783325 | GGGGAGGAGGGCTCT[A/C]TGTTATAGAGTCTCT | 7409 |
rs570161139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6807365 | TTCCCGATAAGGAGC[A/G]CACAAGGTAGATCCC | 7409 |
rs570259896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841134 | TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA | 7409 |
rs570299456 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6828609 | GCCAGGTTCACCCCT[A/G]CCCCCTCCCCAGGAC | 7409 |
rs570370740 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | VAV1 | GRCh38.p7 | 19:6834649 | AGTAATAATATATTA[C/T]AATAATATATAAAAT | 7409 |
rs570386652 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845455 | ACAACATAAAATTAA[C/G]CTTGTAATTGTTACT | 7409 |
rs570394197 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788029 | TGGCAGTGAGCCGAG[A/C]TCCCGCCACTGCACT | 7409 |
rs570441202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817474 | GCCCCACCTCCATCC[A/G]TCTAGTTAACAAACA | 7409 |
rs570473187 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849126 | TTAGAATCAGAGGGC[A/C]CATGTGCAGGTTTGT | 7409 |
rs570475205 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821530 | CAAGAGGCATGGGAT[C/G]TAGCGCCTCAGACAG | 7409 |
rs570494522 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816686 | TAAAATAGACACAGA[C/T]GGGTGTGGTGGCTCA | 7409 |
rs570531344 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6778121 | TCTGTATTTTTAGTA[C/G]AGACAGGGTTTCAGC | 7409 |
rs570586542 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6788556 | TAATTTTTGTATTTT[C/T]AGTAGAGACGGGGTT | 7409 |
rs570587475 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6823526 | TATTTTATATATATT[C/T]TTTGTTATGTTAACC | 7409 |
rs570683739 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6817982 | TGAGCCACCACGCCC[A/G]GCCTTAAATTTGTTT | 7409 |
rs570707344 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787447 | CTCCAAAAATGCTGG[C/G]ATTGCAGGCGTGAGT | 7409 |
rs570713585 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6805842 | AAAGAGAGGAGGAAA[A/G]GAAGGAAGGAAGAAG | 7409 |
rs570714563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821123 | AGAAAGATAGAGGGC[C/T]GGGCGCAGTGGCTCA | 7409 |
rs570733088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834629 | AATATTAATTAATAT[A/G]ATATAGTAATAATAT | 7409 |
rs570798018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6826420 | CTGTGGTGAAATTAC[C/T]GTAGCATTAAATGAG | 7409 |
rs570799851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790400 | AACCACGGATCGGAT[A/G]TCTTAGAACAAAGGA | 7409 |
rs570815147 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6811191 | CAGGCATGCACCACC[A/G]TGCCCGGCTAATTTT | 7409 |
rs570866223 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6791091 | GTGTGTCTCTTACAA[A/G]GACACTTGTTATTGG | 7409 |
rs570910558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849438 | GGATTTACAGGTGCA[C/T]GTCACCATGCCTGGC | 7409 |
rs570924399 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843652 | TTCAGCATTCCTCTC[C/T]GGAAAATAGCTTAAT | 7409 |
rs570959943 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6812090 | TCACATGACTGCATC[C/G]ACATGCAAGGAGAGA | 7409 |
rs571091777 | snp | A/G | 0.000214142 | 0.0103453 | missense | VAV1 | GRCh38.p7 | 19:6833947 | GACAAAAAGAGGAAT[A/G]AGCTGGGTGAGTTGG | 7409 |
rs571126828 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6823276 | GATTACAGGCATGCA[C/T]CACCATGCTCGACTA | 7409 |
rs571151478 | in-del | -/TA | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6822701 | AATATGAGTCTGACG[-/TA]TATATATATATTAAA | 7409 |
rs571161929 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6840430 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 7409 |
rs571219124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836290 | ACCAGCAATGAGTGA[A/G]AATTCCAGTTTCTCC | 7409 |
rs571290234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781137 | CAAACTCCTGGCCTC[A/G]AGAGACCCTCCCACC | 7409 |
rs571330537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6835490 | GCTAGTTGCTACCAT[A/G]TTGGACATATCCATC | 7409 |
rs571355223 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808319 | CTTCATCTCAAAAAA[A/G]AAAGTTCAAAAAAAC | 7409 |
rs571365398 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6775998 | CATATTCATCCATCC[A/G]TTCATCCACCCATCC | 7409 |
rs571426819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775643 | GGCACATTCCTGCCC[C/T]TACCCATTTTGTTGC | 7409 |
rs571502671 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6789900 | CTGCACCTGGCCTTA[-/T]TTTTTTATTTAATGA | 7409 |
rs571539702 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6773605 | CCATCTCAGAGGAGA[C/T]AGTAAGGCAGGGCCC | 7409 |
rs571577807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6842705 | GCGGGTGTGGTGGTG[C/T]GTACCTGTAGTCCCA | 7409 |
rs571587057 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6779940 | CACGGTGAAACCCCG[C/T]CTCTACTAAAAATAC | 7409 |
rs571664435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6850362 | CTTTATATCCTATGG[C/T]TGTCTATATTGGTGG | 7409 |
rs571727496 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6856979 | CCTGAGGTGGGAGGG[A/G]GCCTGCCTGGTGTGT | 7409 |
rs571737319 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6847564 | TGTTTGTTTTACTTA[C/T]TGTCATTTACCTTGA | 7409 |
rs571747402 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773105 | GCTGCTCCACCTCTG[G/T]GCCTGCAAAGGAGAG | 7409 |
rs571755276 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6799667 | GTTTGAATTACTGAT[C/G/T]GCACTTTTGGCTATC | 7409 |
rs571764982 | in-del | -/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6773177 | ACAATCTGAGATTCT[-/G]GGGTGGCCTCCCCAA | 7409 |
rs571922547 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6818571 | AACTGTGTCCCCCCA[A/C]AATTTATACATTGAA | 7409 |
rs571968419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795352 | CAAATGACCCTCCTT[C/T]TCTGAACTCTGTGTA | 7409 |
rs572022278 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6795769 | GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA | 7409 |
rs572031774 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6801034 | TAGCTCTCTGTGCTT[A/C]CCGGCACACCCTCTC | 7409 |
rs572033888 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6840130 | CAACCACCTATTCCC[C/T]TCTCCCAGCCCCTGA | 7409 |
rs572074883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834895 | AGGAGTTTGAGACAA[A/G]CGTGGGCAACAGAAC | 7409 |
rs572084694 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6801388 | ACCAGATCTGCCTGA[C/G]CCTCCCACCGGTGCT | 7409 |
rs572096507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806533 | GGATTCCTTTTCTGG[C/T]TTTGTAAATCTAGGA | 7409 |
rs572099214 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815284 | TCCCAAGTAGCTGGG[A/G]CTACTGGCCATCACA | 7409 |
rs572124075 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813176 | TTCTAATGAGGTTGC[A/C]CACAGATGTCGGCTG | 7409 |
rs572176024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6834106 | ATTTGGGAGGCCAAG[A/G]CGGGAGGATCGCTTG | 7409 |
rs572221422 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817597 | TTATTTGGGTGAGAT[A/G]AACAATAAACACAAC | 7409 |
rs572234624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6807573 | TAACAGACCATGGAC[C/T]GGTACCAGGAGGCTT | 7409 |
rs572235633 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | VAV1 | GRCh38.p7 | 19:6777913 | TCAAGCAATTCTCCT[G/T]CAGCAGCCTCCTGAG | 7409 |
rs572259422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6784773 | TGCTGGGATTACAGA[C/T]GTGAGCCACCATGCC | 7409 |
rs572282690 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6811358 | TTTATTCAATAAATT[A/G]TATTGGGCACTATTG | 7409 |
rs572319669 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790636 | AAGCTGGTGGTGTTA[C/G]CAAGTTTTATTGAAG | 7409 |
rs572358762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806149 | TGGAGTACAGTGGCA[C/T]GATCTCGGCTCACTG | 7409 |
rs572373470 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780026 | TGAAGCAGGAGAATG[A/G]CATGAACCTGGGAGG | 7409 |
rs572400502 | in-del | -/ATCCATCC | 0.0142736 | 0.0832652 | intron-variant | VAV1 | GRCh38.p7 | 19:6776078 | TCCATCCATCCATTT[-/ATCCATCC]ATCCATCCATCCATC | 7409 |
rs572419985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818238 | CTAGAGGAGGTCTCA[C/T]AGAGAAGGTGTCCTT | 7409 |
rs572421652 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848506 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 7409 |
rs572480935 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6824299 | TCTTTAGCTGTTCCC[C/T]TTCAATCTCTTATCT | 7409 |
rs572487784 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6802141 | TGGGAATTGAACAAT[A/G]AGAACACATGGGCAC | 7409 |
rs572508160 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774235 | CAGGTTCACGTCATT[C/T]TCCTGCCTCAGCCTC | 7409 |
rs572516099 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6841496 | TTTTTTTTTTTTTGA[C/T]AGGGAGTTTTGCTCT | 7409 |
rs572528339 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813617 | TTCCCTCTGTAGGAG[A/T]ATATTGGCTACTCAT | 7409 |
rs572580220 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797231 | AGTGAGACTCAGTAT[-/C]AAAAAAAAAAAAAAA | 7409 |
rs572594506 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6849094 | TCCCACCTATATATT[A/T]TTTTTTTCAACTTAT | 7409 |
rs572601902 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817933 | CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAAA | 7409 |
rs572664626 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6803220 | AGAGCAGGGCTACCC[A/C]ACAGGCTGTGAGCCC | 7409 |
rs572690352 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | VAV1 | GRCh38.p7 | 19:6779020 | TAGCTGGGACTACAG[A/G]TGTGCACCGGCATAC | 7409 |
rs572725543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6802756 | GAGGCACAGACTTTG[A/G]GATCCAGTGCTGGTA | 7409 |
rs572737491 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817721 | AGATGGGGTCTCGCT[C/G]TGTTGCCCAGGCTGG | 7409 |
rs572765036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6830853 | AGTACTTTGGGAGGC[C/T]GAGGTGGGAGAATTG | 7409 |
rs572768648 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845883 | CATAGTATATTTATA[C/T]TACAGATTTGCATTT | 7409 |
rs572802081 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6830135 | ACAATCTCGGCTCAC[C/T]GCAACCTCCGCCTCC | 7409 |
rs572815529 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6822790 | CAAAATAAATACAAA[A/T]TCAAAAATATATAAA | 7409 |
rs572819241 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851493 | AGCCCTCAAATATGT[G/T]ATAGATAGAAACCTA | 7409 |
rs572827385 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856190 | TAATCCCAGGTACTC[A/G]TTAAGCTGAGGCAGG | 7409 |
rs572848494 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786420 | TGAACTATGATCCTG[A/C]CACTGCACTCCAGCC | 7409 |
rs572868488 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797960 | AAAAAAACCAGCTAT[A/G]TTGACATACAGTAAA | 7409 |
rs572964308 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786925 | CTAGTAACAATCTAT[A/C]TAAAAATGATCCCTG | 7409 |
rs572979866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6841980 | CCTGTAATCCCAACA[C/T]TTTGGGAGGCCGAGG | 7409 |
rs572984152 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780730 | GCACGTGCCACCACA[A/T]CCGGCTAATTTTTTT | 7409 |
rs573060615 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773347 | GGTCTCGGGGGAGCT[C/T]CCCAGAACCCCCAGG | 7409 |
rs573091577 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797475 | TGGGAGGCCAAGGCG[A/G]GCGGATCATCTGAGG | 7409 |
rs573095405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836691 | TGCCTGGGGAGTGGG[A/G]TAGGTAGACTGAGAC | 7409 |
rs573104694 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6856100 | AGGAGTTTGAGACCC[A/G]CCTGGCCAACATGGC | 7409 |
rs573152237 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6798819 | CCTGGCCTGATTTGA[C/T]AAATTTTGACATATG | 7409 |
rs573172491 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812038 | CCCTGAAAGTGATGC[A/T]TATGACAAATGCTCC | 7409 |
rs573173124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6792012 | GTGTGTGGAACTTAA[A/G]GGGGGGATGGGAAAT | 7409 |
rs573178871 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6838167 | ATCTATATATCATCT[A/T]TCTATTTACCTATCA | 7409 |
rs573219348 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6832487 | TTCCTTCCTCCTCCT[C/T]CTCCTCTTTCTCCTT | 7409 |
rs573224845 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6851083 | GTGTATTTAAATTTT[A/C]CTTACGTATATATAC | 7409 |
rs573275713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804441 | ATTTATTTAGAGACA[A/G]AGTCTTGCTCTGTCG | 7409 |
rs573285078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793853 | AACTAGTCCCTACCT[C/T]ATAGGATTGTTGTAA | 7409 |
rs573289473 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6832000 | GACTGTCATGGGCTT[C/G]CCTGTTCCCTACAGA | 7409 |
rs573352771 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775854 | GAAAAAGGAAAGGTG[A/C]TCCTGTGGAGGAAAT | 7409 |
rs573389578 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834164 | CTAATTTTTTTTTTT[A/T]AAATAGAGATGAGGT | 7409 |
rs573397779 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814852 | GAATCTTTTCAACAT[A/C]TCATTATTAAGTACA | 7409 |
rs573432368 | snp | A/G | 0 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6856610 | GCGCCTGTAATCCCA[A/G]CTACTCGGGATGCTG | 7409 |
rs573559952 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772183 | GGGAGTGGGGAGGGC[A/G]GGGAGGGAACTGGGC | 7409 |
rs573567026 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804052 | AGCAGTAAAAAGATC[A/C]GTAGTTGTCAGAGGT | 7409 |
rs573568614 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6809828 | CAGATAGTTTGGATG[G/T]AGAATCTGAATAATC | 7409 |
rs573606930 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809120 | GGGTCTTGTCTTGTC[A/G]CCCAAGCTGGGGTGC | 7409 |
rs573615059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6829009 | TGGGTGGAGCCTGGG[C/T]AGGGGCGGGGCCGGG | 7409 |
rs573651403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6824230 | TTGGGTGTGAGCCAC[C/T]ACCCCGGCCTTAATT | 7409 |
rs573664993 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6823736 | AGCTCTTTATCCCAG[C/G]CTCAGTCTTTTTCTG | 7409 |
rs573669102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6776608 | CACTCATCCATCCAT[C/T]CATCCATCCATCCAC | 7409 |
rs573678929 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772468 | AGTGTCACTGCCGCC[A/G]TCTGCATATGGAGGA | 7409 |
rs573688018 | in-del | -/ATCT | 0.0178098 | 0.0926698 | intron-variant | VAV1 | GRCh38.p7 | 19:6776234 | TTTATCCATCCACTC[-/ATCT]ATCCATCCATCCATC | 7409 |
rs573697152 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6791435 | TGAGCTATCTCATCT[C/T]AAGGTCCTTGAGCTA | 7409 |
rs573717764 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798551 | CCAGCTACTTGGGAG[C/G]CTGAGATGGGAGGAT | 7409 |
rs573752096 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818324 | TGTTTGCGTGGGTGC[C/T]ACAACAAAGTACCAC | 7409 |
rs573774962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6807471 | GCTCAGGTGGTAATG[C/T]GAGCAATGGGGAGTG | 7409 |
rs573797427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6848403 | TTTTTCCCCTTTTTT[C/T]CTTTTCTTTTCTTTT | 7409 |
rs573836639 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6797629 | AATTGTTTGAACCCC[A/G]GGGGCAGAGGTTGTT | 7409 |
rs573907106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6833036 | CACGATTCAGTGTGG[C/T]CAAAGGGTGAAAACG | 7409 |
rs573930473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773718 | CAGGCTGGAGGGGTG[A/G]TGGTGGATTTGACTG | 7409 |
rs573952332 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6803455 | TTCTGCTCCAGCCCT[A/G]TTTTAGCTAGTCCTC | 7409 |
rs573971943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6843248 | GGAGGAACCTCCGAG[C/T]CAATTAGTTATGCAT | 7409 |
rs573973129 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834463 | TGGGCAGGCTGGTCT[C/T]GAACTCTTGACCTCA | 7409 |
rs573991154 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815103 | CCTAGAATTTAGTAA[C/T]GTTGTTTGAACCATA | 7409 |
rs574011215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6850550 | GTTGGGACAGCTTGT[C/T]TTTGGTTTCCAGTAG | 7409 |
rs574105993 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6809048 | AGACCAACCCAGATA[A/C]AAAAGATGAAGACTT | 7409 |
rs574141374 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6780664 | GGAACCTCCACCTCC[G/T]GGGTTCAAGAGATTC | 7409 |
rs574163711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6818628 | TGGCAGTATTTGGAT[A/G]TGGAGTATTTACAGA | 7409 |
rs574186624 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6837275 | CATTTTTGTGTAAAG[A/G]TCCTTTCCTTCCTAC | 7409 |
rs574202611 | snp | C/T | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857545 | AAGCCCCCTCACCAA[C/T]CACAGACAAAGCCCC | 7409 |
rs574206511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786401 | CAGGAGTTTGAGGCT[G/T]CAGTGAACTATGATC | 7409 |
rs574216248 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849239 | TTTCAGCTCTTTCAT[C/T]CCACCCTCCTCCCTC | 7409 |
rs574240717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816081 | CTGGAGTGCAGTGGC[G/T]CAATCTCGGCTCACT | 7409 |
rs574242594 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810074 | AGTCCCAACACTCAG[A/G]AGGTTGAGGCAAGAG | 7409 |
rs574244741 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6787334 | GTGCACACCACAATG[C/G]CAGGCTAATTTTTGT | 7409 |
rs574247094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6793813 | TCTCTGTGACTCAGT[C/T]TCCCTATCTTTCAAA | 7409 |
rs574271188 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849836 | TTATCCAGTCCACTG[C/T]TGATGGGCACCTGGG | 7409 |
rs574272403 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813781 | TCTTGGGGCTGGGTG[C/T]GGTGGCTCATACCTG | 7409 |
rs574272423 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819026 | GAGGCTGAGACAGGA[G/T]AATTGCTTGAACCTG | 7409 |
rs574305924 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6793283 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCACTGC | 7409 |
rs574337521 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6776685 | ATGTATCCACCCATC[C/T]ACCCACCCACCCATT | 7409 |
rs574339169 | in-del | -/AT | 0.00279162 | 0.0372561 | intron-variant | VAV1 | GRCh38.p7 | 19:6823464 | TATCATTATTTAAAG[-/AT]ATATATATATAAAGT | 7409 |
rs574344031 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6808613 | TTTCCAAGAATACTC[A/G]TCACCATACTCACTT | 7409 |
rs574383298 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793806 | CAGAACCTCTCTGTG[A/C]CTCAGTTTCCCTATC | 7409 |
rs574386090 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821384 | CCAGCCTGGGTGACA[A/G]AGTGAGACTCCGTTA | 7409 |
rs574411097 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6804573 | AGGCGCGTGCCACCA[C/T]GCCTGACTAACTTTT | 7409 |
rs574456151 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848860 | GTGCAGTGGTGAGAT[C/T]TTAGCTCACTGCAAC | 7409 |
rs574463749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844272 | TGCCCAGGCTGGAGC[A/G]CAATGGCGTGATCTC | 7409 |
rs574472253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826523 | AGGTTTCTTCTCCAG[C/T]GGGGAAGAGCAAGGC | 7409 |
rs574553064 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793047 | TCAAGAAAGGACCAT[A/G]TATATGGCCGGGCGC | 7409 |
rs574585395 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771136 | GTGACAGAATGAGAC[C/G]CTGTCAAAAAAAAAA | 7409 |
rs574605704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852176 | GCACTGTCATGCCTG[A/G]CTAATTGTTTAAATC | 7409 |
rs574633106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6781426 | GGAGTTTTGCCAGCT[A/G]GATGGGAAATCAGTG | 7409 |
rs574644017 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831262 | TCCTGTGAACTCTTC[C/T]GTTCGCTTCAGTTTT | 7409 |
rs574683711 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6819335 | TCTGTGAAAACACTT[C/T]GTGATGTGCTGTTTC | 7409 |
rs574686175 | snp | A/G | 2.46363e-05 | 0.00350964 | intron-variant | VAV1 | GRCh38.p7 | 19:6825457 | CACTCTGTCTTGCCT[A/G]GGCTGGGCATCTGAG | 7409 |
rs574797418 | snp | C/T | 0.0189856 | 0.0955633 | intron-variant | VAV1 | GRCh38.p7 | 19:6832578 | TTCCTCCCCTTCCTC[C/T]TCCTCGCCCTCCTCT | 7409 |
rs574864734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783417 | TACTGGGGAAAGAGC[A/G]CTATGAAAGAATTTC | 7409 |
rs574901832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6794752 | GTTATTGCTGTGAAA[C/T]AAACCACTCCAAACT | 7409 |
rs574951680 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809377 | TGAGCCACCATACCC[A/G]GCAATTCTCTTTGGC | 7409 |
rs574952628 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6815466 | TTTCTGTTTGTAGCC[C/T]GTGAGCTTAGTTTTG | 7409 |
rs574968236 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6839006 | CTTCCGGTTTCAAGC[A/G]ATTCTCCTGCCTTAG | 7409 |
rs575001059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6804824 | TGCCTCCCACGTTCA[C/T]GCCATTCTCCTGCTT | 7409 |
rs575005493 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844948 | CTGGGAGTAAGAGGA[G/T]GTGGGTGAGGTGAGT | 7409 |
rs575015665 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793491 | AAACATGGTCTTGGG[C/T]GGCGGCAAGACAGGT | 7409 |
rs575037034 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839558 | CAGGCGTGAGCCACC[A/G]CGCCCGGCTGGGTAT | 7409 |
rs575042056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6814874 | TTAAGTACAGTGTTT[C/T]GGTCTAGGTTTTCTG | 7409 |
rs575097415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6856681 | ATAAGCTGAGATTGC[A/G]CCATTGCACTCCAGC | 7409 |
rs575207366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6809262 | ATTCATTTGTAGAGA[C/T]GGGGTCTTGCTTTGT | 7409 |
rs575216503 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6788735 | ATGTCTATTTCTGAA[C/G]CGGCTGCTGTGGCCA | 7409 |
rs575229857 | snp | C/T | 9.9005e-05 | 0.0070351 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6850745 | AGAGAAAAAGGCTTT[C/T]CGGGGGCTTACGGTA | 7409 |
rs575281950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6781375 | GACTGGCTTCTCTGC[C/T]GCCTCCCCGACAGAC | 7409 |
rs575304387 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6792709 | CTACCATGCATGTCC[A/G]GTGCATGGTTCTTAA | 7409 |
rs575392619 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6844040 | TCTCTGCCCCCATAC[A/T]TTCTTCTTTTCTTCT | 7409 |
rs575423213 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6775864 | AGGTGCTCCTGTGGA[G/T]GAAATGGCATAAATA | 7409 |
rs575504856 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852523 | TCAGGAGATCGAGAC[C/G]ATCCTGGCTAACACG | 7409 |
rs575504933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6831423 | TTCAAGAGATTCTCC[C/T]ACCTCAGCCTCCTGA | 7409 |
rs575544950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6836789 | GCTCTCCAGGCCATC[C/T]TGAGATAGATGGACA | 7409 |
rs575619520 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772720 | GGTAGCACTAGCTGT[C/T]GCTCCACAGGCGAGC | 7409 |
rs575623203 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6826506 | TGGAGAAACTGGGAC[C/T]CAGGTTTCTTCTCCA | 7409 |
rs575658217 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840809 | TTTGAGATGGAGTTT[C/T]GCTCTTGTTGCCCAG | 7409 |
rs575705390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6826005 | TCAAGATCATGCCAC[A/T]GGACTCCAGCCTAGG | 7409 |
rs575711997 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800916 | ACAGGCGTGAGCCAC[C/T]GCACCCAGCCGCTCA | 7409 |
rs575721942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817847 | ACCCGCCACCTTGCC[C/T]GGCTAATTTTTTGTG | 7409 |
rs575778746 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6820615 | TCATTTCCCCTCCAC[A/G]CCAGTCCCCAAGCTA | 7409 |
rs575789902 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | VAV1 | GRCh38.p7 | 19:6856222 | GAATCGCTTGAACCC[A/T]GGAGGCGGAGGCTGT | 7409 |
rs575805019 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6777074 | ATTCATCTATCTATC[A/G]TCCACCTGCCCACCC | 7409 |
rs575840986 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | VAV1 | GRCh38.p7 | 19:6804809 | GCTCACTGCAAGCTC[C/T]GCCTCCCACGTTCAC | 7409 |
rs575905770 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6846782 | TATCTATATTAACAT[A/T]TAGCTATCTACAATA | 7409 |
rs575942145 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6777740 | AGATCTGAGGCCCAG[A/G]GAGAGAATGATACCA | 7409 |
rs576033216 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6845862 | ATCACATATTATACC[A/C]TATATCATAGTATAT | 7409 |
rs576089554 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807141 | TTTTTCCATGGACCA[C/G]AGTTAGGGGGGATGG | 7409 |
rs576089894 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6806024 | GCAAATGACAGAAAA[A/C]CTAATTACAGGTCAA | 7409 |
rs576109804 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798919 | CACCCCTCCCTGCCT[A/C]CCCCTCCTCCCACCT | 7409 |
rs576128229 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6783368 | CTCCATCATCTCATG[A/G]TCTTAGCTTCCCGAA | 7409 |
rs576174314 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6817928 | CCTGACCTCGTGATC[C/T]GCCCGCCTCGGCCTC | 7409 |
rs576175793 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841322 | ACTTTTGCGTATTGT[C/G]AATAAAGCTGCTACA | 7409 |
rs576185507 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838558 | ATCATCTCTCTGCCT[A/G]TTTTTCACCTACCGA | 7409 |
rs576227516 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782719 | TCCCCATCTCTACAA[A/T]ATATATATATATATT | 7409 |
rs576246779 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6811241 | GCATTTCACCATGTC[A/G]GCCAGGCTGGTCTCG | 7409 |
rs576247877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795274 | TGTCTTCCTGGCAGC[A/G]CAAAACAAAGGAAGG | 7409 |
rs576265630 | snp | A/G | 0.176861 | 0.239062 | intron-variant | VAV1 | GRCh38.p7 | 19:6852737 | AAGAAAAAAAAAAAA[A/G]AAAGAAAGAACCTGT | 7409 |
rs576286428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6821229 | ACACAGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7409 |
rs576286465 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | VAV1 | GRCh38.p7 | 19:6816168 | GGGACTACAGGCGCA[C/G]ACCACCACGCCCAGC | 7409 |
rs576288407 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810118 | CAAAAGGTGGAGGCT[A/G]CAGTGAGCTATGATT | 7409 |
rs576342920 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854249 | ACAGGGATGTCATTT[A/G]TGCATTTATGCAACC | 7409 |
rs576386654 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6784734 | CCTGGCCTCAAGTGA[G/T]CTACCCGCCTCGGCC | 7409 |
rs576448889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6816555 | CACACACACACAGAA[C/T]GTGGGTTCTAGATTC | 7409 |
rs576499508 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6847762 | GCTGAGCCATCCCCC[A/C]GAATCCATGTGTCAA | 7409 |
rs576525081 | snp | A/G | 1.6504e-05 | 0.00287258 | intron-variant | VAV1 | GRCh38.p7 | 19:6820658 | GTCAGTTTCTCCCCT[A/G]CCCTTTCGTACTGCC | 7409 |
rs576559059 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6804849 | CTGCTTCAGCCTCCC[A/C]AGTAGCTGGGACTAC | 7409 |
rs576573246 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6827355 | TCACCACAGCCTCGA[C/T]CTCCTGGACTCAAGC | 7409 |
rs576586334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854812 | GGAGTGGATCAGGAT[A/G]ACTTCTGAAAGGCCA | 7409 |
rs576597018 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848559 | AGGCGCCTGTGACCA[A/T]GCCCAGCTAATTTTT | 7409 |
rs576658829 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844742 | GCGCCGAGATGTGGT[C/T]AATGGGGTGGGGACC | 7409 |
rs576666326 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6784189 | AGCCCAGGAGTTTGA[G/T]GCTGCAGTGAGCTAT | 7409 |
rs576684537 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846994 | TCTCAGCTCACTGCA[A/G]CCTCCGCCTACCGAG | 7409 |
rs576685106 | snp | C/T | 1.67607e-05 | 0.00289483 | intron-variant | VAV1 | GRCh38.p7 | 19:6821775 | GCCCCTGGCTCACAC[C/T]CTCCTGACCCCCCAG | 7409 |
rs576736614 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | VAV1 | GRCh38.p7 | 19:6782900 | AAGAAAAAAAAAAAA[A/G]GCCAGGTGCAGTGGC | 7409 |
rs576756468 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771543 | GCGGATCATGAGATC[A/G]GGAGATCGAGACCAC | 7409 |
rs576789241 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6810684 | CACTCTGGCCTGGGC[A/G]ACAAGAGTGAAACGT | 7409 |
rs576805975 | snp | G/T | 3.30169e-05 | 0.00406293 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821675 | CGCCCAGAACAGGGG[G/T]ATCATGTGAGTAACC | 7409 |
rs576817812 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | VAV1 | GRCh38.p7 | 19:6777046 | AGGTGTGAGCCATAC[A/G]CCCGGCCCATCCATT | 7409 |
rs576858674 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6852700 | CACTCCAGCCTGGGC[A/G]ACAGAGCCAGACTCC | 7409 |
rs576882258 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785520 | TATTTTTAGTAGAGA[C/T]GGAGTTTCACCATGT | 7409 |
rs576885818 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771986 | AGGGGATTTAGGAAG[A/G]CCTCATGAGAAGGTA | 7409 |
rs576905606 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829129 | TGGAGTCAACACAGA[C/T]CTGGGAGGAGCCTGG | 7409 |
rs576924535 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784260 | AGACCCTGTCTCTAA[A/C]TATATCTATGCAGGT | 7409 |
rs576950877 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6852324 | CTGGCCTGATGATGA[C/T]TGCTAATTGTAAATT | 7409 |
rs576965985 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6822078 | ATGGCCCTGCCCTGG[A/G]GCTTGGAGGGACATG | 7409 |
rs576984294 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800857 | GTCTTGAACCCCTGA[C/T]CTCAAGTGATCCGCC | 7409 |
rs577022855 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | VAV1 | GRCh38.p7 | 19:6816120 | CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT | 7409 |
rs577044253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6800466 | AGGCGTGTTCCACCA[C/T]ACCCAGCTAATTTTG | 7409 |
rs577046805 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | VAV1 | GRCh38.p7 | 19:6799253 | GCTCACTGCAACCTC[C/T]GCCTCCCAGGTTCAA | 7409 |
rs577087318 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6827233 | CCCAGGCAGCATTTG[C/T]CACATTCCAGTGGGT | 7409 |
rs577087762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6825968 | GAATTGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 7409 |
rs577204121 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6790032 | AATACAAAAAAATTA[C/G]CCGGCCATGGTGGCA | 7409 |
rs577222258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6817646 | GGGATAGAAAACGCC[A/G]GAGTAGGGGTGTGGG | 7409 |
rs577287058 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809823 | TGTGACAGATAGTTT[A/G]GATGTAGAATCTGAA | 7409 |
rs577357828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6833069 | CCAAAAGCCAATCAA[C/T]GAATGAGTGGACACG | 7409 |
rs577396708 | in-del | -/GTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827247 | GCCACATTCCAGTGG[-/GTTT]GTTTGTTTGTTTGTT | 7409 |
rs577403814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6839567 | GCCACCACGCCCGGC[C/T]GGGTATGGCATTTTC | 7409 |
rs577426907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6784647 | TACAGGCAAGTGCCA[C/T]CACACCTAGCTGATT | 7409 |
rs577465383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6795234 | TATCTAGGAGCAGGG[C/T]GCAAAGGAGCCTGGG | 7409 |
rs577469477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6833415 | ATCTTCTGCTTCTCC[A/G]TCACTCTCCTGATCT | 7409 |
rs577597646 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6774703 | GCCTTCCAAAGTGCT[C/G]GAATTACAGGTGTGA | 7409 |
rs577609734 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6832507 | TCTTTCTCCTTCTCC[-/T]TTCCTCCTCCTCTTT | 7409 |
rs577639566 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6829665 | GGACAGGTGGGCATG[A/G]CCAAGTTGGCCAAGG | 7409 |
rs577659029 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | VAV1 | GRCh38.p7 | 19:6791406 | CTTGAGCTAGCTCCT[C/T]ATCTCGAGGTCCTTG | 7409 |
rs577707388 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779838 | AATAAAAGGCCGGGC[A/G]CGGTGACTCACACCT | 7409 |
rs577744714 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6773153 | CCAGGGCTGGCCCAG[A/G/T]GGGTGGTCACAATCT | 7409 |
rs577759982 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | VAV1 | GRCh38.p7 | 19:6802868 | GAGATTTATTCATTC[A/G]ACAGATTTTATTGAG | 7409 |
rs577800852 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6854193 | GAAGGTGAGGTGCGG[C/G]TCCCATGGAGATCTC | 7409 |
rs577848409 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | VAV1 | GRCh38.p7 | 19:6785636 | TGCACATGGTCAGTG[A/G]CCAGGTTTCTTTCTT | 7409 |
rs577921911 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6849742 | ACCCAGTGCATCCAC[A/G]CTGCTGCAATGCACA | 7409 |
rs577974514 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6808060 | GCTCAAGCCTATAAT[C/G]CCAGCACTTTGGGAG | 7409 |
rs577998214 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815206 | GGGCCGGAGTGCAGT[C/G]GTGCGATCATAGCTC | 7409 |
rs578021110 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | VAV1 | GRCh38.p7 | 19:6806641 | TAAATCACTGTCCCA[A/G]AAGCTGGAGCTTAAG | 7409 |
rs578087723 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798244 | ATCGCATCATTGCAC[A/T]CCAGCCTGGGCAACA | 7409 |
rs578101046 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6786035 | TCCCAACTTCCCATT[C/G]TCTTTCATGTTTTAT | 7409 |
rs578149849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6813693 | AATGAAAAGCCATTC[C/T]GGGGTTTTTAATTGA | 7409 |
rs578171052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | VAV1 | GRCh38.p7 | 19:6855615 | ATCCAGCCAACATCT[A/G]TTCATCCATTTCTAT | 7409 |
rs578192531 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840965 | GTATTTTTAGTAGAG[A/G]CAGGGTTTCACCATG | 7409 |
rs745309850 | snp | A/G | 1.65045e-05 | 0.00287263 | intron-variant | VAV1 | GRCh38.p7 | 19:6828586 | GAGCCTGGGTCGGCT[A/G]TTGGGGGGCCAGGTT | 7409 |
rs745339110 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831807 | TTGAACAGAAAAATC[A/G]ATGATGAGTGACATG | 7409 |
rs745400668 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776452 | CATCCATCCACCCAC[C/T]CATCCACCCACCCAT | 7409 |
rs745430064 | snp | A/C | 0.00010123 | 0.0071137 | missense | VAV1 | GRCh38.p7 | 19:6822306 | TATGAGGACCTCATG[A/C]GCTCGGAGCCCGTGT | 7409 |
rs745431466 | in-del | -/TTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840304 | TCAGAATTTTCTTTC[-/TTT]TTTTTTTTTTTTTTG | 7409 |
rs745431526 | snp | A/G | 1.64803e-05 | 0.00287052 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6854060 | ATCCTTAACAAGAAG[A/G]GACAGCAAGGCTGGT | 7409 |
rs745434288 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844887 | CCAAAAAAATTTCGA[A/G]ATGAACAAATACCAA | 7409 |
rs745442652 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812035 | GTGCCCTGAAAGTGA[G/T]GCTTATGACAAATGC | 7409 |
rs745452971 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778338 | GGAAAGATCCACCAG[A/G]ACATGGGAGCTGGTT | 7409 |
rs745485658 | snp | A/G | 6.9e-05 | 0.00587327 | intron-variant | VAV1 | GRCh38.p7 | 19:6822398 | AGGCCCCCCAACACC[A/G]GCCTCTCCCCTCGCT | 7409 |
rs745557782 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806660 | CTGGAGCTTAAGATC[A/C]GGGATTTGCACTCTC | 7409 |
rs745565957 | snp | C/T | 0.000115677 | 0.00760427 | missense | VAV1 | GRCh38.p7 | 19:6836537 | ACATTGTGGAGCTCA[C/T]GAAGGCTGAGGCTGA | 7409 |
rs745581914 | in-del | -/CTC | 9.89968e-05 | 0.00703481 | intron-variant | VAV1 | GRCh38.p7 | 19:6857036 | GGTTGCACTGATGAA[-/CTC]CTCGTCTGTTTCCAG | 7409 |
rs745605832 | snp | A/C | 5.0885e-05 | 0.0050438 | intron-variant | VAV1 | GRCh38.p7 | 19:6832209 | TGGCCATGTGAGTCC[A/C]CGTCTTCCTCCCTCT | 7409 |
rs745636807 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800944 | TCACCATCTCTTTGT[C/T]GCCTGCATGGCACCA | 7409 |
rs745647904 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810387 | TAGATTCGTTCCTGG[C/T]TTGTAGACGATCACC | 7409 |
rs745655697 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789681 | TGGCTCACTGCAACC[A/T]CCGCATCATGGGTTC | 7409 |
rs745718351 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6825659 | GTGCCTCCTAGGCTG[G/T]TGGTGAGGGTTGACT | 7409 |
rs745761439 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838016 | AGGAATTTCCAACCC[C/T]ATCATTCTTTCCAAA | 7409 |
rs745800973 | in-del | -/ATTTATTTACCAATAAACCAACGGTAAATGATTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794044 | AACCAACGGTAAATG[lengthTooLong]ATTTACCAATAAACC | 7409 |
rs745817637 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799030 | GGTACCATCTGTGGT[C/G]TTCTGTGACTGGCTG | 7409 |
rs745830320 | snp | A/G | 4.95127e-05 | 0.00497533 | missense | VAV1 | GRCh38.p7 | 19:6850677 | GGTTCCAGATATAAC[A/G]TCGAGGTCAAGCACA | 7409 |
rs745905228 | snp | A/C | 1.64754e-05 | 0.00287009 | intron-variant | VAV1 | GRCh38.p7 | 19:6833879 | AGGCTGGGCATAGGT[A/C]GACAGGCTTTCTTTG | 7409 |
rs745940589 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810709 | AAACGTTATCTCAAA[A/G]AAAAAAAATTACTCT | 7409 |
rs746006694 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819199 | ACAGAATGGAACCTG[A/T]GTTTTGATTCAACAA | 7409 |
rs746012151 | snp | A/G | 3.29478e-05 | 0.00405867 | missense | VAV1 | GRCh38.p7 | 19:6829880 | CTGCACAGCTTCCAG[A/G]TTCGGGATGACTCTT | 7409 |
rs746057541 | snp | A/G | 1.69467e-05 | 0.00291085 | intron-variant | VAV1 | GRCh38.p7 | 19:6825160 | TCTTGGGTCTGTCTA[A/G]TGCGGATAACCTGCT | 7409 |
rs746069093 | snp | C/T | 1.68207e-05 | 0.00290001 | intron-variant | VAV1 | GRCh38.p7 | 19:6832051 | TGCTCCCACCCTCTG[C/T]GGGGGCAGTGCCTTC | 7409 |
rs746129844 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831245 | CTTCCTTCTGCTTTT[G/T]CTCCTGTGAACTCTT | 7409 |
rs746160173 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830383 | ACCTACTATATCCAG[G/T]GCACTCTTCTAGGCA | 7409 |
rs746168471 | snp | C/T | 1.66286e-05 | 0.0028834 | intron-variant | VAV1 | GRCh38.p7 | 19:6773059 | TGGAGACGGGGGTCC[C/T]CCCCGGGGCTGACAG | 7409 |
rs746202527 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803817 | TGATCCAGCCACGTC[A/G]GCCTCCCAAAGTGCT | 7409 |
rs746205153 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824347 | ACCACGAGCTTACTC[A/G]CTGTCTCTGTGGATT | 7409 |
rs746253966 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814054 | GACAGAGTGATACCC[C/T]GTCTCTAAAAATAAA | 7409 |
rs746258621 | snp | C/T | 1.64833e-05 | 0.00287078 | intron-variant | VAV1 | GRCh38.p7 | 19:6820686 | GCCCCACCCTCATTT[C/T]TCTGTCTCCTCACAG | 7409 |
rs746273765 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848120 | TCAGCATTAAGTAAC[G/T]CCTTTCTCCCTGACT | 7409 |
rs746275305 | in-del | -/ACACACACACACACACACACAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836836 | AGCAGAGAGATGGAC[-/ACACACACACACACACACACAC]ACACACACACACACA | 7409 |
rs746293013 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806592 | CAGTTGCTCCAGACC[A/G]CCTAACCTCACTCTT | 7409 |
rs746294162 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841855 | CACATCCTTGCCAAC[A/G]TTTGCTACTTTCTGT | 7409 |
rs746307916 | in-del | -/CATCCATCCATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776597 | ATCCGTCCATCCACT[-/CATCCATCCATC]CATCCATCCATCCAC | 7409 |
rs746388456 | snp | C/T | 5.28947e-05 | 0.00514242 | intron-variant | VAV1 | GRCh38.p7 | 19:6833520 | TTTATGTGTTCCCTG[C/T]ATCTCAGAGGTACCT | 7409 |
rs746412253 | snp | A/G | 1.65018e-05 | 0.00287239 | missense | VAV1 | GRCh38.p7 | 19:6828452 | CAGGAGGCGATGGAG[A/G]AGGAGAACCTGCGGC | 7409 |
rs746436167 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772502 | TCACCCATCTCATAG[C/T]CTAGCTGGCCTGACT | 7409 |
rs746473671 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843615 | TGTATGACCTTGGGC[C/T]GGTTACTTAACCTCC | 7409 |
rs746507161 | snp | C/G | 1.81227e-05 | 0.00301015 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772806 | CTGGGCAGGCGGTAG[C/G]CATGGAGCTGTGGCG | 7409 |
rs746507744 | snp | C/T | 9.96429e-05 | 0.00705773 | intron-variant | VAV1 | GRCh38.p7 | 19:6836572 | AACTGGTGGGAGGTA[C/T]AGGCTGGGGCCACAA | 7409 |
rs746568352 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842964 | CTGGGGCAGTCTCTC[A/C]CCCGAGGTTCTGGGA | 7409 |
rs746601564 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832287 | TCCCTACTCTGTCCT[C/G]ACATGCCATGGGACC | 7409 |
rs746618868 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775662 | CCATTTTGTTGCCCT[C/T]TGAAGCCCGGCCGTG | 7409 |
rs746629469 | in-del | -/ATCCATCCATCCATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777235 | TTTATCTGTTTAACT[-/ATCCATCCATCCATCC]ATCCATCCATCCATC | 7409 |
rs746635696 | in-del | -/GGGGCT | 3.59479e-05 | 0.00423942 | intron-variant | VAV1 | GRCh38.p7 | 19:6832244 | GTCCACAGAGGGGCA[-/GGGGCT]GGGAAGGAGGAACGT | 7409 |
rs746661562 | snp | A/G | 1.6483e-05 | 0.00287076 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772945 | CCTTCTGTGTCAGCT[A/G]CTTAACAACCTGCTA | 7409 |
rs746664454 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6825531 | TGTGTGTTCATGGGC[A/G]AGGGGCTGCCCATCT | 7409 |
rs746706346 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812124 | GAAATGCAGTCCTTA[G/T]CTGGGCAGCCATTTT | 7409 |
rs746717800 | snp | C/T | 0.000117352 | 0.00765913 | intron-variant | VAV1 | GRCh38.p7 | 19:6833178 | TTTTTAATTTTCCCC[C/T]GCCAGCTCCAACATC | 7409 |
rs746722878 | in-del | -/TCAATGTCCGC | 1.65482e-05 | 0.00287643 | intron-variant | VAV1 | GRCh38.p7 | 19:6850765 | GGCTTACGGTAAGGG[-/TCAATGTCCGC]TCAATCCCAGCTTTC | 7409 |
rs746741669 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837820 | CTTTACCCCTAAATA[C/T]TTCTTAAGAGCAAGA | 7409 |
rs746753599 | snp | C/G | 4.31062e-05 | 0.00464233 | intron-variant | VAV1 | GRCh38.p7 | 19:6826753 | CCTCTCCCGCTCCTC[C/G]CCAGGCCCTGGGGGC | 7409 |
rs746830286 | snp | A/G | 3.32044e-05 | 0.00407444 | intron-variant | VAV1 | GRCh38.p7 | 19:6850774 | TAAGGGTCAATGTCC[A/G]CTCAATCCCAGCTTT | 7409 |
rs746842824 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810661 | AGTGAGCTGAGATCA[C/T]GTCATTGCACTCTGG | 7409 |
rs746843986 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797234 | GAGACTCAGTATCAA[-/A]AAAAAAAAAAAAAAA | 7409 |
rs746864533 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836705 | GGTAGGTAGACTGAG[A/G]CTTCTGGGCATGGCT | 7409 |
rs746975687 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | VAV1 | GRCh38.p7 | 19:6833744 | AGAAGGTAAGACTTT[C/T]CCGTGGTCCTTCCTG | 7409 |
rs746995262 | snp | C/T | 1.67593e-05 | 0.00289471 | intron-variant | VAV1 | GRCh38.p7 | 19:6852946 | TGGGATAGCATCTGC[C/T]ATGTGGTCCGCCTTC | 7409 |
rs747040293 | snp | G/T | 3.35171e-05 | 0.00409358 | intron-variant | VAV1 | GRCh38.p7 | 19:6832053 | CTCCCACCCTCTGCG[G/T]GGGCAGTGCCTTCAG | 7409 |
rs747080804 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845068 | ACTCGAACCAGATTT[A/G]CATTCGTTTTTTAAA | 7409 |
rs747091292 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781188 | GATGATAATCGTGAA[C/T]CATCGTGCTCCACCC | 7409 |
rs747143456 | snp | C/T | 1.65696e-05 | 0.00287828 | missense | VAV1 | GRCh38.p7 | 19:6825340 | ACTTCCTAAAGGAGA[C/T]GAAGGAAGCCCTGGG | 7409 |
rs747148078 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818913 | CTGAGGTCAAGAGTT[C/T]AAGACCAGCCTGACC | 7409 |
rs747202428 | snp | G/T | 1.64765e-05 | 0.00287019 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6820713 | ACAGTTCCTGTGCCT[G/T]AAGAACATTAGAACC | 7409 |
rs747202497 | snp | A/G | 5.64265e-05 | 0.00531132 | intron-variant | VAV1 | GRCh38.p7 | 19:6826597 | TTTACCTGGTGGCCT[A/G]TCTTCTCCCTGTAGG | 7409 |
rs747221808 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841681 | GGGTTTTGCCATGTT[A/G]GTCAGGCTGGTCTTG | 7409 |
rs747230801 | snp | C/G | 1.65272e-05 | 0.0028746 | intron-variant | VAV1 | GRCh38.p7 | 19:6848134 | CTCCTTTCTCCCTGA[C/G]TCATACCCTTTTGGG | 7409 |
rs747279989 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840494 | GTATTTTTAGTAGAG[C/T]TTCACCGTGTTAGCC | 7409 |
rs747319718 | snp | C/G | 1.74461e-05 | 0.00295343 | missense | VAV1 | GRCh38.p7 | 19:6833533 | TGCATCTCAGAGGTA[C/G]CTTCTATCAGGGCTA | 7409 |
rs747321751 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855645 | TCTGTGCATCCATCC[A/G]TCTATCCATGCATGC | 7409 |
rs747327166 | snp | A/G | 3.29614e-05 | 0.00405951 | intron-variant | VAV1 | GRCh38.p7 | 19:6820850 | AAGCCCAAAGACTGA[A/G]TTTCAGTTAATTTCT | 7409 |
rs747336613 | snp | C/T | 1.65776e-05 | 0.00287898 | intron-variant | VAV1 | GRCh38.p7 | 19:6850659 | AGGGCCCGGTGACCA[C/T]CTGGTTCCAGATATA | 7409 |
rs747355716 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772172 | AGGGGGAGAGAGGGA[A/G]TGGGGAGGGCAGGGA | 7409 |
rs747396179 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810119 | AAAAGGTGGAGGCTG[C/T]AGTGAGCTATGATTG | 7409 |
rs747416717 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824759 | CTGGTCTTGAACTCC[C/T]GACCTCGTGATCCAC | 7409 |
rs747491692 | snp | C/T | 6.59707e-05 | 0.00574291 | intron-variant | VAV1 | GRCh38.p7 | 19:6828744 | GGGCCAGGGGTGTGG[C/T]CACGTGGGGAGAGTG | 7409 |
rs747519627 | snp | C/T | 1.65203e-05 | 0.002874 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6854092 | GCGAGGGGAGATCTA[C/T]GGCCGGGTGAGGCAG | 7409 |
rs747525457 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784674 | GATTTTTGTATTTTT[A/G]GTAGAGACGGGGTTT | 7409 |
rs747556837 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796211 | CACTCCAAGGATATG[A/G]GTCTACTGCCTTCAG | 7409 |
rs747561694 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841902 | TTTTTGCCTTATAGT[A/G]GCTGTCCTAATTGTT | 7409 |
rs747594041 | in-del | -/G | 1.64798e-05 | 0.00287047 | intron-variant | VAV1 | GRCh38.p7 | 19:6828794 | GGGAGACCCTTGCTA[-/G]ACCCCCTGCCTACTG | 7409 |
rs747601332 | snp | C/G | 3.29484e-05 | 0.00405871 | missense | VAV1 | GRCh38.p7 | 19:6843154 | CTCCTCAGGACCTGT[C/G]TGTTCATCTCTGGTG | 7409 |
rs747646628 | snp | G/T | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857386 | TGGTGTCGTTCAGAA[G/T]GACCTGCTAGGAGAG | 7409 |
rs747654381 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814490 | TACTGACACTTAGTA[C/T]ACTTTGTATACTGGT | 7409 |
rs747675683 | snp | C/T | 1.6534e-05 | 0.00287519 | intron-variant | VAV1 | GRCh38.p7 | 19:6773037 | CGCGGGCAGGTGTGC[C/T]GAGGGTTGGAGACGG | 7409 |
rs747683889 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779950 | CCCCGTCTCTACTAA[A/C]AATACAAAAAATTAG | 7409 |
rs747743260 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776524 | ATCCATCCTCTCATC[-/CATC]CATCCATCCATCCAT | 7409 |
rs747813611 | snp | A/G | 1.67416e-05 | 0.00289318 | intron-variant | VAV1 | GRCh38.p7 | 19:6828193 | GGCACATCTCTAGGC[A/G]TGGGCTCCACGTACC | 7409 |
rs747917503 | snp | A/G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834314 | AGTGGTGTGATCTTG[A/G/T]CTCACTACAACCTCC | 7409 |
rs747922153 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835067 | AAAAAATAAATATAT[A/G]AAATCTATGAATGGG | 7409 |
rs747923618 | in-del | -/CCAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776443 | CATCCATCCATCCAT[-/CCAC]CCACCCACCCATCCA | 7409 |
rs747928469 | snp | A/G | 1.66222e-05 | 0.00288285 | intron-variant | VAV1 | GRCh38.p7 | 19:6852956 | TCTGCCATGTGGTCC[A/G]CCTTCTAGGAGCTGG | 7409 |
rs747930438 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | VAV1 | GRCh38.p7 | 19:6833917 | TTCCAGGACAAACTA[C/T]ATCGCAGGGCTCAGG | 7409 |
rs747961615 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809891 | ATCCTCCATTTCCAG[A/C]CAGGTGCAGTGGCTC | 7409 |
rs747980456 | snp | C/T | 1.73039e-05 | 0.00294137 | intron-variant | VAV1 | GRCh38.p7 | 19:6853110 | CTGGGGGCTTACAGC[C/T]TCAGCCCCTTCCCAT | 7409 |
rs748005101 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847703 | TTCAGGAAATGCCTG[A/G]TGAAGCCATCGCCAA | 7409 |
rs748016704 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818425 | CCTCTTCTTCCTCCT[C/T]GCCCACTCTAACTCC | 7409 |
rs748053053 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781033 | CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGACTA | 7409 |
rs748056357 | snp | A/G | 3.29636e-05 | 0.00405964 | intron-variant | VAV1 | GRCh38.p7 | 19:6829924 | CAACAAGAAGGTGGG[A/G]CTTTGACGCCGGAAC | 7409 |
rs748056412 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817772 | GCTCACCGCAGCCTC[C/T]ACCTCCTGGGCTCCA | 7409 |
rs748135092 | snp | C/T | 1.67553e-05 | 0.00289437 | intron-variant | VAV1 | GRCh38.p7 | 19:6836398 | TTGAAAGTTGACTGC[C/T]AACCACCCTGTACTC | 7409 |
rs748173540 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827888 | GTGGTTCTCAAGCTG[C/T]CCCCACCTCATGGAG | 7409 |
rs748214081 | snp | C/T | 3.30699e-05 | 0.00406618 | intron-variant | VAV1 | GRCh38.p7 | 19:6850667 | GTGACCATCTGGTTC[C/T]AGATATAACGTCGAG | 7409 |
rs748215772 | in-del | -/TATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838299 | CATCTACATATTATC[-/TATC]TATCTATCTATCTAT | 7409 |
rs748216879 | snp | C/T | 9.40159e-05 | 0.00685559 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826618 | TCCCTGTAGGTTCCT[C/T]GTCTATGGCCGCTAC | 7409 |
rs748233422 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791163 | TCTTAAATATCTCCT[C/T]ATCTTGAAGTCCTTG | 7409 |
rs748257070 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845370 | AGCCTGGGCAACAGA[C/G]CGAGACTCGGTCTCA | 7409 |
rs748336456 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773460 | CCCCCACATGTGTCT[A/C]CTCCTCCCGGGCCCT | 7409 |
rs748336672 | snp | C/G | 1.65165e-05 | 0.00287367 | intron-variant | VAV1 | GRCh38.p7 | 19:6833636 | GCAAGGTACGAGTGG[C/G]AGGGAGGCTGGGAGG | 7409 |
rs748372205 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854327 | GTCGAGGAGACAGAA[A/G]CAAGCACGGTACAAG | 7409 |
rs748383031 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812607 | AGTGAGCCAAGATCA[C/T]GCCACTGCACTCCAG | 7409 |
rs748440399 | snp | G/T | 1.64895e-05 | 0.00287132 | intron-variant | VAV1 | GRCh38.p7 | 19:6828755 | GTGGCCACGTGGGGA[G/T]AGTGTGTGTCTGGCT | 7409 |
rs748442945 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784298 | AATCTCAATGGGATG[C/T]AGAATAAGAAGGACC | 7409 |
rs748490225 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776463 | CCACCCATCCACCCA[C/T]CCATCCATCCATCCA | 7409 |
rs748527771 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793399 | AAAGCAGAGGGAGCC[A/G]AGACACCAAAGAATG | 7409 |
rs748562822 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820302 | GTGCAGTGGTGCCAT[C/T]ATAGCTCACCGCAGG | 7409 |
rs748566930 | snp | C/G | 1.67267e-05 | 0.0028919 | intron-variant | VAV1 | GRCh38.p7 | 19:6828912 | ACAGGTGGGTGGAGT[C/G]AACATGGATCTGGGA | 7409 |
rs748566978 | snp | A/G | 0.000103056 | 0.00717755 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6822484 | GCAGACGGAGGAGAA[A/G]TACACTGACACGCTG | 7409 |
rs748582926 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771958 | AATGCGGAAAAGGCT[A/G]TGATTTGAAATGAGG | 7409 |
rs748629227 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795290 | CAAAACAAAGGAAGG[G/T]GATGAGTCATTAACC | 7409 |
rs748652362 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783660 | GCTAATTTTGTAGGG[G/T]TTTCTCCATGTTAGT | 7409 |
rs748677954 | snp | A/C/G | 3.31759e-05 | 0.00407272 | intron-variant | VAV1 | GRCh38.p7 | 19:6833300 | GGTGAGAATCTGGGA[A/C/G]GAGGGTCCTGCATAC | 7409 |
rs748705299 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807353 | TCAGGCACCAGATTC[C/T]CGATAAGGAGCGCAC | 7409 |
rs748721670 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832441 | CTCCTCTTTCTTGTT[A/C]TCCTCTCCTCTTCCT | 7409 |
rs748725050 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785497 | CCACCATGCCTGGCT[A/G]ATTTCTGTATTTTTA | 7409 |
rs748749110 | snp | A/G | 3.29837e-05 | 0.00406088 | intron-variant | VAV1 | GRCh38.p7 | 19:6820671 | CTGCCCTTTCGTACT[A/G]CCCCACCCTCATTTC | 7409 |
rs748848963 | snp | C/T | 1.6525e-05 | 0.00287441 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6852968 | TCCGCCTTCTAGGAG[C/T]TGGTGGAGTTTTACC | 7409 |
rs748929867 | snp | A/G | 1.65015e-05 | 0.00287237 | intron-variant | VAV1 | GRCh38.p7 | 19:6828578 | TTAGGTAGGAGCCTG[A/G]GTCGGCTGTTGGGGG | 7409 |
rs748951046 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808618 | AAGAATACTCATCAC[C/T]ATACTCACTTGCCAG | 7409 |
rs748977005 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800813 | GTGTGTGTGTGTGCA[G/T]TCGGGGTTTCACCAT | 7409 |
rs748978595 | snp | C/T | 1.64749e-05 | 0.00287005 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6854032 | GTCGCTCAAGGAGGG[C/T]GACATCATCAAGATC | 7409 |
rs749003491 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780667 | ACCTCCACCTCCTGG[A/G]TTCAAGAGATTCTCC | 7409 |
rs749058401 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778485 | GGTGGTGGCTTTGGA[A/G]AGCCACACCTGGGTT | 7409 |
rs749080960 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807622 | GAGGCTGAGGTGGGA[G/T]GATCACTTGAGCCCA | 7409 |
rs749134426 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817249 | TGGTATTTTTAGTAG[A/C]AATGGGGTTTCACCA | 7409 |
rs749141431 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799173 | TTTTTTGTTTGTTTC[A/G]CTTTGTTTTTTTGAG | 7409 |
rs749148300 | snp | G/T | 1.67416e-05 | 0.00289318 | intron-variant | VAV1 | GRCh38.p7 | 19:6832056 | CCACCCTCTGCGGGG[G/T]CAGTGCCTTCAGTCT | 7409 |
rs749148436 | snp | C/T | 1.65105e-05 | 0.00287315 | missense | VAV1 | GRCh38.p7 | 19:6836515 | TTTCTACGGCTCAAC[C/T]CTGGAGACATTGTGG | 7409 |
rs749155012 | snp | C/G | 1.66715e-05 | 0.00288712 | missense | VAV1 | GRCh38.p7 | 19:6825361 | AAGCCCTGGGCACCC[C/G]TGGCGCAGCCAATCT | 7409 |
rs749160383 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827660 | TTGGAGTGAAGTGGT[A/G]TGATCTCAGCTCAAT | 7409 |
rs749185598 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790856 | TCTTTGCCATGGAAG[C/G]GGGCATCAGCTTCTG | 7409 |
rs749187719 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777380 | TGTTGAGGAGCCTGC[A/T]TTCTAGTGGGGGAGG | 7409 |
rs749211248 | snp | A/C/G | 0.000725834 | 0.0190378 | intron-variant | VAV1 | GRCh38.p7 | 19:6826733 | GCCGGGCCACTTCTC[A/C/G]GGGGCCTCTCCCGCT | 7409 |
rs749226528 | in-del | -/GT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856877 | TAGGAGGTAATGGGT[-/GT]GTGTGTGTGTGTGTG | 7409 |
rs749341841 | snp | C/T | 1.67587e-05 | 0.00289466 | intron-variant | VAV1 | GRCh38.p7 | 19:6821776 | CCCCTGGCTCACACC[C/T]TCCTGACCCCCCAGG | 7409 |
rs749366175 | snp | C/G | 1.65405e-05 | 0.00287576 | intron-variant | VAV1 | GRCh38.p7 | 19:6850763 | GGGGCTTACGGTAAG[C/G]GTCAATGTCCGCTCA | 7409 |
rs749421363 | snp | C/T | 1.64751e-05 | 0.00287007 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833724 | AGATTTCCCAGGAAC[C/T]ATGAAGAAGGTAAGA | 7409 |
rs749490530 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810950 | TTGCAATGAAAAGGC[A/G]TGCTTTCAACTGTTG | 7409 |
rs749495954 | in-del | -/AT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823465 | TATCATTATTTAAAG[-/AT]ATATATATAAAGTAT | 7409 |
rs749538243 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820185 | TTAGCTGGGTGTTGC[A/G]ACACATGACTGAAGT | 7409 |
rs749551935 | snp | A/G | 1.64803e-05 | 0.00287052 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825061 | CCCGCAGCATTTCTT[A/G]AAGCCCCTGCAACGG | 7409 |
rs749589708 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832333 | CTCTTCATTTGGGAA[A/G]TAAGAGGGACAGGCC | 7409 |
rs749591622 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819362 | TTTCATATCACAGAA[C/T]GGGACCTGTGTTTTG | 7409 |
rs749595885 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796292 | CAAAGGCTTCAAAAT[C/T]ATTTATTTGTCCTTC | 7409 |
rs749604125 | snp | A/G | 1.64727e-05 | 0.00286986 | missense | VAV1 | GRCh38.p7 | 19:6829851 | ACTCCTATGACCTCA[A/G]GGACTTTGTAAACCT | 7409 |
rs749665885 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848315 | GATATGATTCCTATA[A/G]AGGCTCAAAAAGGCT | 7409 |
rs749701288 | snp | C/G | 1.64787e-05 | 0.00287038 | intron-variant | VAV1 | GRCh38.p7 | 19:6843201 | TTTGTTTCAATGAGA[C/G]GTTTCTGGGTTGGGG | 7409 |
rs749721964 | snp | C/T | 1.69175e-05 | 0.00290834 | intron-variant | VAV1 | GRCh38.p7 | 19:6825153 | CCAGCCCTCTTGGGT[C/T]TGTCTAGTGCGGATA | 7409 |
rs749769554 | snp | C/T | 0.000165736 | 0.00910167 | intron-variant | VAV1 | GRCh38.p7 | 19:6773050 | GCTGAGGGTTGGAGA[C/T]GGGGGTCCTCCCCGG | 7409 |
rs749771918 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806369 | GGATTCCAGGCGTGA[A/G]CCACCATGCACGGCC | 7409 |
rs749824961 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815318 | GGCTAATTTTTGTAT[G/T]TTTTGCAGAGACAGT | 7409 |
rs749873095 | snp | C/T | 1.64972e-05 | 0.00287199 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6850742 | CACAGAGAAAAAGGC[C/T]TTCCGGGGGCTTACG | 7409 |
rs749873161 | snp | A/G | 1.6566e-05 | 0.00287797 | missense | VAV1 | GRCh38.p7 | 19:6833614 | TCCCTCCATGTGGCC[A/G]ACATGGGCAAGGTAC | 7409 |
rs749876872 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775403 | ACGAGGGTGCATGAT[A/G]CTAATCCCTGGGAGA | 7409 |
rs749907213 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805774 | TGCACACACACTATA[A/T]GAATATTATATATAG | 7409 |
rs749973046 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829178 | TCCTAGATGAGCAGG[A/T]GGGTGGAGTCAACAC | 7409 |
rs749995859 | snp | A/T | 1.64741e-05 | 0.00286998 | intron-variant | VAV1 | GRCh38.p7 | 19:6833693 | CCCGTTCTCACCATT[A/T]CCTTTACCCTCCCGT | 7409 |
rs750007730 | snp | A/G | 1.64944e-05 | 0.00287175 | intron-variant | VAV1 | GRCh38.p7 | 19:6828727 | AGGCGGTGGAGCCGG[A/G]TGGGCCAGGGGTGTG | 7409 |
rs750009405 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787946 | GCCGGGTGTGGTGAC[A/G]GGCACCTGTAGTCCC | 7409 |
rs750014628 | snp | C/T | 1.64969e-05 | 0.00287196 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828862 | GATCGACGGGGAACT[C/T]AAGATCACCTCGGTG | 7409 |
rs750086060 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803753 | TATTTTTAGTAGAGA[C/T]GGGATTTCACCATGT | 7409 |
rs750088385 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823286 | ATGCACCACCATGCT[A/C]GACTAATTTTTGTAT | 7409 |
rs750111597 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840978 | AGACAGGGTTTCACC[A/G]TGTTGGCCAGGCTGG | 7409 |
rs750161086 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813063 | AAGTAACAAATTATC[C/T]CCAAACTTAATTGTA | 7409 |
rs750164147 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802353 | AATAATAATAAAATT[A/T]AAAAAAATAAAGGAC | 7409 |
rs750181509 | snp | C/G/T | 3.29817e-05 | 0.00406078 | intron-variant | VAV1 | GRCh38.p7 | 19:6829766 | AGAGCCAGACAGGAA[C/G/T]GCGTTATCCATCCTT | 7409 |
rs750219357 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801466 | GACGGGCTTCCTCAC[A/G]GAAGGGTTTGAGGGC | 7409 |
rs750236444 | snp | A/G | 1.66571e-05 | 0.00288587 | missense | VAV1 | GRCh38.p7 | 19:6825119 | ATCTTTATCAACATT[A/G]AGGTGAGCCGGCCGA | 7409 |
rs750242990 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854154 | TTGAGCTGGTGGTGG[A/G]CGAGACTGGAACTGG | 7409 |
rs750290415 | in-del | -/TTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844048 | CCATACTTTCTTCTT[-/TTC]TTCTTCTTCTTCTTC | 7409 |
rs750302024 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant | VAV1 | GRCh38.p7 | 19:6843125 | TTGGGGTCTCTCTCT[C/G]TATTCTTAGGGCCCT | 7409 |
rs750310334 | snp | A/G | 1.78535e-05 | 0.00298771 | intron-variant | VAV1 | GRCh38.p7 | 19:6847955 | AATATGGGGACCCAG[A/G]CACGGGGACCGTGCC | 7409 |
rs750340566 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852402 | CTGGTAAATTTATCA[C/T]GAAGTAAGTTAGTCC | 7409 |
rs750343513 | snp | A/T | 1.70801e-05 | 0.00292229 | intron-variant | VAV1 | GRCh38.p7 | 19:6833170 | TTTTTTTTTTTTTAA[A/T]TTTCCCCTGCCAGCT | 7409 |
rs750366818 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794704 | TTCACAACAAATCCA[C/T]GGTGTTGGCACCATC | 7409 |
rs750391927 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820992 | TTGAGTTCCTGCTCT[A/G]ACACTTGCTGTGTGA | 7409 |
rs750420989 | snp | A/G | 3.29881e-05 | 0.00406115 | intron-variant | VAV1 | GRCh38.p7 | 19:6828503 | GTGAGTGGGTGTAGG[A/G]TGCTGGTGACTCACC | 7409 |
rs750428732 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795828 | AGCTGGGACTACAGG[C/T]GCGTGCCACCGCGCC | 7409 |
rs750453895 | snp | C/T | 1.6795e-05 | 0.0028978 | intron-variant | VAV1 | GRCh38.p7 | 19:6821893 | GGCCGCACAGCTCAC[C/T]GGAGCACCGTCCTGG | 7409 |
rs750553569 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844564 | GTAGCAGGTGCACTA[C/T]TGCCATTTATAAAAA | 7409 |
rs750559304 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807125 | GTTTTGTGGAAGACA[A/G]TTTTTCCATGGACCA | 7409 |
rs750587103 | snp | C/T | 1.66513e-05 | 0.00288537 | intron-variant | VAV1 | GRCh38.p7 | 19:6853940 | CACTTCTGTTCTCTC[C/T]CCACAGTGGGAAGCA | 7409 |
rs750632166 | snp | A/C/T | 3.30136e-05 | 0.00406273 | missense | VAV1 | GRCh38.p7 | 19:6836492 | CACCCCCTGGAGCCA[A/C/T]TGGACCCTTTCTACG | 7409 |
rs750659829 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780738 | ACCACATCCGGCTAA[-/T]TTTTTTTGTATTTTT | 7409 |
rs750662170 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827690 | TGCCATCTCTGCCTC[C/T]CGGGTTCAAGCAATT | 7409 |
rs750663421 | in-del | -/CATCCAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838428 | ATCCATCCATCCATC[-/CATCCAT]CCATCTATCATCTAT | 7409 |
rs750675586 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816566 | AGAACGTGGGTTCTA[G/T]ATTCATACCATCTCG | 7409 |
rs750689372 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800621 | AGCTTCTTTTTTTTG[C/T]TTTGTTTTGTTTTTT | 7409 |
rs750717851 | in-del | -/AA | 1.8285e-05 | 0.00302361 | intron-variant | VAV1 | GRCh38.p7 | 19:6833168 | TTTTTTTTTTTTTTT[-/AA]TTTTCCCCTGCCAGC | 7409 |
rs750781267 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775338 | ATAGACTTAAGGATG[A/T]ACTTCCATTCTTGTG | 7409 |
rs750827919 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789238 | TATTTATTTTAATTT[A/C]TTTCTTTCTCTCTCC | 7409 |
rs750834221 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787766 | CCATGCCCAACTGTT[C/T]TTTTAATGTTTTAAA | 7409 |
rs750844704 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829934 | GTGGGGCTTTGACGC[A/C]GGAACTATGGGGTCC | 7409 |
rs750851881 | snp | A/G | | | utr-variant-3-prime | VAV1 | GRCh38.p7 | 19:6857196 | GCTGTGACAGCTCCC[A/G]GCGGGTGGAGACTTT | 7409 |
rs750861548 | snp | A/G/T | 6.71389e-05 | 0.00579352 | intron-variant | VAV1 | GRCh38.p7 | 19:6825133 | TGAGGTGAGCCGGCC[A/G/T]ATCCCCAGCCCTCTT | 7409 |
rs750870866 | in-del | -/TTATGT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781502 | GCTGAGCCTCTTTCC[-/TTATGT]TTAAGAGCTATTTAT | 7409 |
rs750889633 | snp | A/C | 3.29576e-05 | 0.00405928 | intron-variant | VAV1 | GRCh38.p7 | 19:6820841 | GCACACTTGAAGCCC[A/C]AAGACTGAGTTTCAG | 7409 |
rs750919975 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837496 | CCCTCGCTCTTCATG[A/G]TGACTTCAGATCTCT | 7409 |
rs750953925 | snp | A/C | 0.00010015 | 0.00707567 | intron-variant | VAV1 | GRCh38.p7 | 19:6850649 | CCCCAGACTCAGGGC[A/C]CGGTGACCATCTGGT | 7409 |
rs750969275 | in-del | -/TGCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776125 | ATCCATCCATCCATC[-/TGCT]CATCCATTCATCCAT | 7409 |
rs750986727 | snp | A/G/T | 3.29871e-05 | 0.00406112 | missense | VAV1 | GRCh38.p7 | 19:6821629 | CGTCACAGGTCATCT[A/G/T]CACCCTGTCTGCTCT | 7409 |
rs750990794 | in-del | -/G | 1.64944e-05 | 0.00287175 | intron-variant | VAV1 | GRCh38.p7 | 19:6828494 | GCCATGAGGGTGAGT[-/G]GGTGTAGGGTGCTGG | 7409 |
rs751026534 | snp | C/T | 9.88435e-05 | 0.00702937 | intron-variant | VAV1 | GRCh38.p7 | 19:6833765 | GTCCTTCCTGTGTAC[C/T]ACAAATAATGGGCAA | 7409 |
rs751028226 | snp | A/G | 3.30797e-05 | 0.00406679 | missense | VAV1 | GRCh38.p7 | 19:6828882 | TCACCTCGGTGGAAC[A/G]GCGCTCCAAGATGGA | 7409 |
rs751078934 | snp | A/T | 1.64833e-05 | 0.00287078 | intron-variant | VAV1 | GRCh38.p7 | 19:6829773 | GACAGGAATGCGTTA[A/T]CCATCCTTCCAGGTA | 7409 |
rs751118002 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839621 | AGAACTAGGTAGAGG[C/T]GGTGATTCCTCATTC | 7409 |
rs751146908 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815707 | GCTGCCTGAGTTTGT[A/G]TCCCGGCTGTGTGTC | 7409 |
rs751163988 | snp | C/T | 1.6734e-05 | 0.00289253 | intron-variant | VAV1 | GRCh38.p7 | 19:6825128 | AACATTGAGGTGAGC[C/T]GGCCGATCCCCAGCC | 7409 |
rs751197515 | in-del | -/CA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835212 | GTGTATATATATATA[-/CA]TACACACACACACAC | 7409 |
rs751213058 | snp | A/G | 1.65296e-05 | 0.00287481 | intron-variant | VAV1 | GRCh38.p7 | 19:6773033 | CCTCCGCGGGCAGGT[A/G]TGCTGAGGGTTGGAG | 7409 |
rs751213851 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840306 | AGAATTTTCTTTCTT[-/T]TTTTTTTTTTTTTTG | 7409 |
rs751242560 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839021 | GATTCTCCTGCCTTA[A/G]CCTCCTGAGTAGCTA | 7409 |
rs751251885 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852156 | ATAGCTGAGACTACA[A/G]GCATGCACTGTCATG | 7409 |
rs751269790 | snp | A/G | 3.35368e-05 | 0.00409479 | intron-variant | VAV1 | GRCh38.p7 | 19:6825279 | TGGGCTCTGGTCCCA[A/G]CCCTCACCCTTCCCT | 7409 |
rs751283015 | snp | C/G | 0.000148254 | 0.00860844 | missense | VAV1 | GRCh38.p7 | 19:6843150 | GGCCCTCCTCAGGAC[C/G]TGTCTGTTCATCTCT | 7409 |
rs751341642 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784082 | AACATACCAAGGTCC[C/T]GTCTCTACAAAAAAT | 7409 |
rs751380383 | in-del | -/AGAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6821112 | GAGGATTAAATAGAA[-/AGAT]AGAGGGCCGGGCGCA | 7409 |
rs751389377 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811413 | TTCAGAGGTGACTCA[A/G]CCCTGGGTCCTGACT | 7409 |
rs751398430 | snp | A/G | 0.00171379 | 0.0292226 | intron-variant | VAV1 | GRCh38.p7 | 19:6784278 | TATCTATGCAGGTCT[A/G]TGGAAATCTCAATGG | 7409 |
rs751417273 | snp | A/C | 1.7886e-05 | 0.00299044 | intron-variant | VAV1 | GRCh38.p7 | 19:6833483 | AATATTTGGCCCTGT[A/C]TGTAAAGGTCACTCG | 7409 |
rs751438783 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795006 | TATCTCCAAGTGGCT[C/T]GGGCTTCCCCACAAC | 7409 |
rs751482177 | snp | A/C | 8.32092e-05 | 0.00644963 | intron-variant | VAV1 | GRCh38.p7 | 19:6828386 | GGAGAAGGGGAGGGG[A/C]CCAGGTGACGTCTGA | 7409 |
rs751518842 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850284 | AGGAGTGGAGGTCTT[C/T]TCCAAGGCCCCTTTT | 7409 |
rs751523777 | snp | C/T | 3.30251e-05 | 0.00406343 | missense | VAV1 | GRCh38.p7 | 19:6836506 | ATTGGACCCTTTCTA[C/T]GGCTCAACCCTGGAG | 7409 |
rs751527514 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831092 | CTGTCTCTATTAAAA[A/C]ATAAATGAATGAAAC | 7409 |
rs751537311 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832018 | TGTTCCCTACAGAGG[C/G]AGGGGTGGGTGGGTG | 7409 |
rs751565720 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793860 | CCCTACCTTATAGGA[G/T]TGTTGTAAGAATTAA | 7409 |
rs751586832 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843355 | GTCCCTCACCTTGGG[A/C]GATGATGGTCTTGTT | 7409 |
rs751599909 | snp | C/T | 0.000122752 | 0.00783333 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772782 | GGCTGCGAGGGTGCA[C/T]GGCCGGCCCTGGGCA | 7409 |
rs751648659 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847655 | TCCCCTACTTCTGTC[C/T]GGGTGACCACAGAGA | 7409 |
rs751679096 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831964 | TACAAGGATATCCAT[C/G]CATGGTGCTAGGGGC | 7409 |
rs751695726 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815196 | TGTGTTGCCTGGGCC[A/G]GAGTGCAGTGGTGCG | 7409 |
rs751717825 | snp | A/T | 1.64784e-05 | 0.00287035 | intron-variant | VAV1 | GRCh38.p7 | 19:6836937 | TGGCAGGTGGGGTTA[A/T]GGATCCTATAACCTC | 7409 |
rs751718238 | in-del | -/C | 4.00986e-05 | 0.00447747 | intron-variant | VAV1 | GRCh38.p7 | 19:6826732 | CGCCGGGCCACTTCT[-/C]GGGGGCCTCTCCCGC | 7409 |
rs751725873 | in-del | -/CCATCCA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838431 | CATCCATCCATCCAT[-/CCATCCA]TCTATCATCTATCTA | 7409 |
rs751745817 | snp | A/C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856985 | GTGGGAGGGAGCCTG[A/C/T]CTGGTGTGTGGAGGG | 7409 |
rs751763871 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775155 | CCCCCACCAACCTAA[A/G]CATCCATCCTCTGGC | 7409 |
rs751773152 | snp | C/G | 1.82374e-05 | 0.00301966 | intron-variant | VAV1 | GRCh38.p7 | 19:6832247 | CACAGAGGGGCAGGG[C/G]CTGGGAAGGAGGAAC | 7409 |
rs751848856 | in-del | -/TTTT | 0.000100407 | 0.00708472 | intron-variant | VAV1 | GRCh38.p7 | 19:6833152 | AAAATACTGACCTTC[-/TTTT]TTTTTTTTTTTTAAT | 7409 |
rs751918885 | snp | A/G | 1.90667e-05 | 0.00308755 | intron-variant | VAV1 | GRCh38.p7 | 19:6826715 | ATGAAGCTGGAGGTG[A/G]GCGCCGGGCCACTTC | 7409 |
rs751973855 | snp | C/T | 1.64955e-05 | 0.00287184 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821633 | ACAGGTCATCTACAC[C/T]CTGTCTGCTCTGTCC | 7409 |
rs751974047 | snp | C/T | 1.6489e-05 | 0.00287128 | intron-variant | VAV1 | GRCh38.p7 | 19:6828072 | TTGTTCTCTGATTCC[C/T]CAGGAATGTTCTCAG | 7409 |
rs752034769 | snp | G/T | 1.64754e-05 | 0.00287009 | intron-variant | VAV1 | GRCh38.p7 | 19:6833703 | CCATTTCCTTTACCC[G/T]CCCGTAGATTTCCCA | 7409 |
rs752052267 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781731 | TCGTGCCTCAGCCTC[A/T]CAAGTAGCTGAGATT | 7409 |
rs752213783 | snp | C/T | 1.64977e-05 | 0.00287203 | intron-variant | VAV1 | GRCh38.p7 | 19:6829954 | CTATGGGGTCCTCCA[C/T]GCAGTCGGCAGCTTA | 7409 |
rs752257527 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851779 | GGCCCTTGAGAAGCT[A/G]AGTCCTCTGAAAGAA | 7409 |
rs752268580 | snp | A/G | 1.65581e-05 | 0.00287728 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848073 | GACTTTCTTGGTGCG[A/G]CAGAGGGTGAAGGAT | 7409 |
rs752287565 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800725 | CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 7409 |
rs752296162 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798455 | CAACATGGTGAGACC[A/G]GCCTCATCTCTAATA | 7409 |
rs752301784 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837755 | TCTACCCACACATAG[C/T]ATTTATTTTTCCTGG | 7409 |
rs752354969 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811287 | GTGATCCACCCTCTT[C/T]GGCCTCCCATAGTGC | 7409 |
rs752408018 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819715 | ATGGAGAGTGTTGGG[A/G]GTTGTGGGAGAGGCC | 7409 |
rs752421908 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818897 | GAGGCGGGTGGATCA[C/T]CTGAGGTCAAGAGTT | 7409 |
rs752424814 | in-del | -/TCTA/TCTATCTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838093 | TCATCTGTCTGTCTG[-/TCTA/TCTATCTA]TCTGTCTATCTATCT | 7409 |
rs752547196 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | VAV1 | GRCh38.p7 | 19:6828534 | TGCTGCAGACACCCT[C/T]CTGGTAGGGGCTGAT | 7409 |
rs752552285 | snp | G/T | 1.66324e-05 | 0.00288374 | missense | VAV1 | GRCh38.p7 | 19:6833593 | ACAAGGAGTGTCTGG[G/T]GAGGGTCCCTCCATG | 7409 |
rs752557737 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776520 | ATCCATCCATCCTCT[-/CATC]CATCCATCCATCCAT | 7409 |
rs752581104 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830905 | TCAGCCTGGGCAACA[C/T]AGGGAGATCCCCGTC | 7409 |
rs752582540 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805771 | ATATGCACACACACT[A/G]TATGAATATTATATA | 7409 |
rs752635200 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792803 | TTGGCAATGCCTGGA[A/G]ACAGTTTCAGTTATC | 7409 |
rs752651058 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798051 | GGAGGCCGAGGTGGG[C/T]AAATCACTTGAGGCC | 7409 |
rs752656112 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | VAV1 | GRCh38.p7 | 19:6854001 | ATGACTTCTGCGCCC[A/G]AGACCGATCAGAGCT | 7409 |
rs752674851 | snp | G/T | 1.64882e-05 | 0.00287121 | missense | VAV1 | GRCh38.p7 | 19:6828671 | ACAACGAGACACTGC[G/T]ACAGATCACCAATTT | 7409 |
rs752703738 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830103 | CTCGCTCTGTCGCCA[A/G]GCCGGAGTGCAGTGG | 7409 |
rs752707217 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | VAV1 | GRCh38.p7 | 19:6843093 | CTCTGCTGTCAAGCT[A/G]GGGTCTTTACACTAA | 7409 |
rs752707524 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842400 | TGCAACTCTTCAGCT[C/T]CGCCCCTGTAGTGCA | 7409 |
rs752719107 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775017 | GTGATCTGACCACCT[C/T]GGCCTCTCGAAAGGC | 7409 |
rs752740786 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773199 | CCTCCCCAAGCTTAA[C/T]AGGCTCCCTGTGTGG | 7409 |
rs752755675 | in-del | -/CA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777341 | GGACAGTGGGAATAG[-/CA]CACACACACACAAAA | 7409 |
rs752759285 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824256 | TAATTTTAGAACGTT[G/T]TCATCATCTCCCAAA | 7409 |
rs752775188 | in-del | -/C | 1.75139e-05 | 0.00295916 | intron-variant | VAV1 | GRCh38.p7 | 19:6822385 | GGGGGCAGCCCCAGG[-/C]CCCCCCAACACCGGC | 7409 |
rs752775726 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779226 | CTGGCTAATTTTTTA[-/T]TTTTTTGTAGAGATG | 7409 |
rs752779871 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855541 | TCCACTCACGCATCT[A/G]TCTAACCATCTATCC | 7409 |
rs752795410 | snp | A/G | | | missense | VAV1 | GRCh38.p7 | 19:6850747 | AGAAAAAGGCTTTCC[A/G]GGGGCTTACGGTAAG | 7409 |
rs752815368 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813246 | TTCCTGAGTGGCTGG[A/G]CCACATAGAGCTTCA | 7409 |
rs752833866 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833167 | TTTTTTTTTTTTTTT[A/T]AATTTTCCCCTGCCA | 7409 |
rs752883433 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852796 | ATAGTCCTGGCTGCT[A/C]AGGGAGGTGATGAAC | 7409 |
rs752883867 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836095 | GCCAGTCTGGTCTCA[A/G]ACTCCTGACCTCAGG | 7409 |
rs752959423 | snp | C/T | 1.70365e-05 | 0.00291855 | intron-variant | VAV1 | GRCh38.p7 | 19:6828215 | CCACGTACCTACTCT[C/T]CTGTGTCTATAAAAG | 7409 |
rs753036503 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796679 | CCTTTACTGAAATGC[C/T]ACTCTCTCAATGAGG | 7409 |
rs753037641 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834206 | GCCCAGCCATACTGT[A/G]TAAATTAAATCATAC | 7409 |
rs753038721 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785283 | CTCAAGTGATCCTCT[C/T]GCCTCTGCCTCCCAA | 7409 |
rs753043052 | snp | C/G/T | 5.13223e-05 | 0.00506546 | intron-variant | VAV1 | GRCh38.p7 | 19:6852928 | CCTTATGGGCTGGCC[C/G/T]GCTGGGATAGCATCT | 7409 |
rs753059692 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | VAV1 | GRCh38.p7 | 19:6833776 | GTACCACAAATAATG[A/G]GCAACAGCGCGGGGA | 7409 |
rs753060124 | snp | C/T | 1.67309e-05 | 0.00289226 | intron-variant | VAV1 | GRCh38.p7 | 19:6821765 | CAGCCCCCAGGCCCC[C/T]GGCTCACACCCTCCT | 7409 |
rs753076667 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849285 | CTACTGTTTCCAGCC[-/TT]TTTTTTTTTTTTTTT | 7409 |
rs753086973 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809394 | CAATTCTCTTTGGCT[G/T]GTAGGAGCTGGAAAG | 7409 |
rs753110859 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6829825 | TCTACTCATCTGTAA[A/G]CGCAGGGGAGACTCC | 7409 |
rs753159743 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817592 | ACATTTTATTTGGGT[C/G]AGATAAACAATAAAC | 7409 |
rs753178432 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844783 | CAGGGAGGCTCTCTC[A/G]TGGGTGCAAGATTTA | 7409 |
rs753225970 | snp | A/G | 1.64762e-05 | 0.00287016 | intron-variant | VAV1 | GRCh38.p7 | 19:6833976 | GGCAGGGGTTGCTGT[A/G]TGGGGGCAGGAGGAA | 7409 |
rs753232757 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785743 | CAGCTCACCGCAACC[C/T]CTGCCTCCTGGGCCC | 7409 |
rs753262849 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778138 | GACAGGGTTTCAGCA[C/T]GTTGGCCAGGCTGGT | 7409 |
rs753328759 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836304 | AAAATTCCAGTTTCT[C/T]CACGTCCTTGTCAAC | 7409 |
rs753331935 | snp | A/G | 3.30289e-05 | 0.00406366 | missense | VAV1 | GRCh38.p7 | 19:6848104 | GCAGCAGAATTTGCC[A/G]TCAGCATTAAGTAAC | 7409 |
rs753340238 | snp | C/G | 1.75752e-05 | 0.00296433 | missense | VAV1 | GRCh38.p7 | 19:6825392 | CTACCAGGTCTTCAT[C/G]AAATACAAGGAGAGG | 7409 |
rs753357973 | snp | G/T | 1.64727e-05 | 0.00286986 | intron-variant | VAV1 | GRCh38.p7 | 19:6850633 | GGGGAATGGGCCTGG[G/T]CCCCAGACTCAGGGC | 7409 |
rs753411061 | snp | C/T | 1.65971e-05 | 0.00288067 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833603 | TCTGGGGAGGGTCCC[C/T]CCATGTGGCCGACAT | 7409 |
rs753432988 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782779 | CCCGGCTACCTAGGA[C/T]GCTGAGGCAGGAGGA | 7409 |
rs753443823 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818330 | CGTGGGTGCCACAAC[A/C]AAGTACCACGAGCTT | 7409 |
rs753445386 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809685 | ATTTGCTGTATGAAG[A/G]TGGGCTGGGAGGAGT | 7409 |
rs753459696 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772665 | CTCCTCCTCCTCCAC[C/T]CCCTCTCAGGGCGAC | 7409 |
rs753469733 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781841 | TCAAACTCCTGACCT[C/T]GAGTGATCCACCCGT | 7409 |
rs753491603 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818838 | AGAAACAAACTGGCC[A/G]GGCGTGGTGGCTCAC | 7409 |
rs753505869 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814735 | TTTCTTTCTTTCCTT[-/C]TTTCCCTCTGTCTTG | 7409 |
rs753530907 | in-del | -/CTTCCTCCCCTTCCTCCTCCTCGCCCTCCTCTTCCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832561 | CTTCCTCCTCCTCTC[lengthTooLong]CTTCCTCCCCTTCCT | 7409 |
rs753544009 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803308 | GGCAGATTATGCAAA[A/T]TTCTAGGAAAAGGGT | 7409 |
rs753634638 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794546 | TAACCAGATGGGTGT[G/T]GTGTCAAGAGACCAA | 7409 |
rs753650216 | snp | G/T | 3.29979e-05 | 0.00406175 | intron-variant | VAV1 | GRCh38.p7 | 19:6828716 | AGAACCTGGTGAGGC[G/T]GTGGAGCCGGGTGGG | 7409 |
rs753703343 | snp | A/C | 9.94085e-05 | 0.00704942 | intron-variant | VAV1 | GRCh38.p7 | 19:6822376 | GGCGTGGGCGGGGGG[A/C]AGCCCCAGGCCCCCC | 7409 |
rs753734529 | snp | A/G | 1.6757e-05 | 0.00289452 | intron-variant | VAV1 | GRCh38.p7 | 19:6854132 | GGTGACGGGGAGGGC[A/G]TGGGGGTTGAGCTGG | 7409 |
rs753740110 | snp | C/T | 1.65241e-05 | 0.00287433 | utr-variant-3-prime, synonymous-codon | VAV1 | GRCh38.p7 | 19:6857123 | GCCCTGGTGCCTTGG[C/T]AGAGAGACGAGAAAC | 7409 |
rs753758099 | snp | A/G | 3.2975e-05 | 0.00406035 | missense | VAV1 | GRCh38.p7 | 19:6772913 | TGTGAACTGGCCCAG[A/G]CCCTCCGGGATGGTG | 7409 |
rs753759341 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802458 | TGCTGCTGTCTGATG[C/G]AGCCCCTTTCTTTAG | 7409 |
rs753824609 | snp | C/G | 0.000136846 | 0.00827068 | intron-variant | VAV1 | GRCh38.p7 | 19:6822552 | CTGCCGGGCGCATGC[C/G]CGGGAGCTGGGCCGG | 7409 |
rs753827846 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809376 | ATGAGCCACCATACC[C/T]GGCAATTCTCTTTGG | 7409 |
rs753834385 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785194 | TCTTTTTTCGGAGAA[A/G]GGGGTCTTGCTCTAT | 7409 |
rs753846566 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812503 | CTACTAAAAAGAAAA[C/T]ACAAAAATTAGCAGG | 7409 |
rs753859595 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855442 | TCTATCCACAAATCA[C/T]CCATTCATCTGTGCA | 7409 |
rs753876214 | snp | A/C | 1.64779e-05 | 0.00287031 | missense | VAV1 | GRCh38.p7 | 19:6828120 | GTTCACCCTGCGGGA[A/C]CTGCTGATGGTGCCT | 7409 |
rs753902811 | snp | C/G | 4.76497e-05 | 0.00488084 | missense | VAV1 | GRCh38.p7 | 19:6822297 | GACGAGATCTATGAG[C/G]ACCTCATGCGCTCGG | 7409 |
rs753912681 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854226 | ACGGTGGGAGGGAAG[G/T]AAGGGACACAGGGAT | 7409 |
rs753929575 | snp | A/G | 1.66629e-05 | 0.00288638 | intron-variant | VAV1 | GRCh38.p7 | 19:6828373 | GCCCTCCCCGCAGGG[A/G]GAAGGGGAGGGGCCC | 7409 |
rs753947740 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6825713 | CACATAGTAGATGCT[C/T]AATAAGTATTTGTTA | 7409 |
rs753959811 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795919 | CAAACTCCTGACCTC[C/G]TGATCCGCCCGTCTC | 7409 |
rs753960517 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834122 | CGGGAGGATCGCTTG[A/G]AGTCAGGTGCACACC | 7409 |
rs754071795 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779568 | CATTAGTCTAAACCA[A/G]GGAGGGGCCTGGCTG | 7409 |
rs754086556 | snp | A/G | 1.67747e-05 | 0.00289605 | intron-variant | VAV1 | GRCh38.p7 | 19:6821878 | AGTGCTCAGGCCTGT[A/G]GCCGCACAGCTCACT | 7409 |
rs754164195 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844675 | AACACGTAAGAGGCA[A/G]GGTCAGGATTTGAAT | 7409 |
rs754213569 | snp | A/C/G | 3.30111e-05 | 0.00406259 | intron-variant | VAV1 | GRCh38.p7 | 19:6829961 | GTCCTCCACGCAGTC[A/C/G]GCAGCTTAGCCCTCT | 7409 |
rs754215510 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843450 | TGGTGATGGTAATGA[C/T]AGTTCCAGTTGTTTT | 7409 |
rs754263910 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777946 | TCTGGGATTACAGGC[A/G]CCTGCCACCACGCCT | 7409 |
rs754272718 | snp | A/G | 1.65754e-05 | 0.00287879 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825308 | CTCCGAGTAGGACCT[A/G]CTTCGTGTTCATACT | 7409 |
rs754314420 | snp | A/C/G | 3.30591e-05 | 0.00406554 | missense | VAV1 | GRCh38.p7 | 19:6836467 | TTTCAGGAATACTAC[A/C/G]GGCTTCCTCCACCCC | 7409 |
rs754326770 | in-del | -/TCTC | 1.6478e-05 | 0.00287032 | intron-variant | VAV1 | GRCh38.p7 | 19:6843116 | TACACTAAGTTGGGG[-/TCTC]TCTCTGTATTCTTAG | 7409 |
rs754343672 | snp | A/C | 1.65026e-05 | 0.00287246 | missense | VAV1 | GRCh38.p7 | 19:6832105 | GTGGAGCCACATGTT[A/C]CTCCTGATCGAGGAC | 7409 |
rs754356904 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816659 | ACCGATCTAAGCCTG[C/T]TTTCTTGTAGGTAAA | 7409 |
rs754416121 | in-del | -/TCAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776284 | CATTCATCTATCCAC[-/TCAT]CCATCCATCCATCCA | 7409 |
rs754417067 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798308 | TTTGGTAAACAATTT[C/T]TTCTTTAATTTCTAG | 7409 |
rs754418537 | in-del | -/TCATCCAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776284 | CATTCATCTATCCAC[-/TCATCCAT]CCATCCATCCATCCA | 7409 |
rs754462714 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836361 | AAATTTTAGCCATTC[A/T]CGTGGGTGGCAAGAT | 7409 |
rs754467896 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6829801 | GTATGCCTTCCTGCT[C/T]GACAAAGCTCTACTC | 7409 |
rs754474771 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837658 | AAGCTATGAGAATAA[C/T]GCAAAGAGCTCCTGT | 7409 |
rs754502281 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824453 | CGTAGTGTTTTCAAG[G/T]TTCATCCACATTGTA | 7409 |
rs754518416 | snp | C/T | 6.66711e-05 | 0.00577331 | utr-variant-3-prime | VAV1 | GRCh38.p7 | 19:6857157 | AGGCTCTGAGCCCGG[C/T]GTGGGCAGGCAGCGG | 7409 |
rs754519854 | snp | A/G | 3.34739e-05 | 0.00409095 | intron-variant | VAV1 | GRCh38.p7 | 19:6825129 | ACATTGAGGTGAGCC[A/G]GCCGATCCCCAGCCC | 7409 |
rs754577854 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785662 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTT | 7409 |
rs754591068 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809817 | CTTAGATGTGACAGA[C/T]AGTTTGGATGTAGAA | 7409 |
rs754659045 | snp | C/T | 0.0071029 | 0.0591693 | intron-variant | VAV1 | GRCh38.p7 | 19:6784287 | AGGTCTGTGGAAATC[C/T]CAATGGGATGTAGAA | 7409 |
rs754670349 | snp | A/G | 1.6764e-05 | 0.00289512 | intron-variant | VAV1 | GRCh38.p7 | 19:6833179 | TTTTAATTTTCCCCT[A/G]CCAGCTCCAACATCT | 7409 |
rs754693037 | snp | C/T | 1.65302e-05 | 0.00287486 | intron-variant | VAV1 | GRCh38.p7 | 19:6773034 | CTCCGCGGGCAGGTG[C/T]GCTGAGGGTTGGAGA | 7409 |
rs754720635 | snp | A/G | 3.30327e-05 | 0.0040639 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833265 | GACCACATCCTGCAA[A/G]GCCTGTCAGATGCTG | 7409 |
rs754758953 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805985 | GTGTTCCATCAAGGC[A/G]GTGGCTATGCTCCCA | 7409 |
rs754777718 | snp | C/G | 3.31559e-05 | 0.00407147 | intron-variant | VAV1 | GRCh38.p7 | 19:6828403 | CAGGTGACGTCTGAC[C/G]TCTTGGTTCTCTCAG | 7409 |
rs754809636 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830091 | TTAAGATGGAGTCTC[A/G]CTCTGTCGCCAGGCC | 7409 |
rs754829013 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850388 | GGTGGAAGGGGAGGT[C/T]TCTTCGTATCCATTC | 7409 |
rs754867940 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791719 | GACAAAACGCTGGCA[C/T]ATTGTAATAAATGTC | 7409 |
rs754873679 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773135 | GGGAATATGCTTACA[C/G]GTCCAGGGCTGGCCC | 7409 |
rs754996497 | snp | A/G | 1.71226e-05 | 0.00292592 | intron-variant | VAV1 | GRCh38.p7 | 19:6853101 | GGTCTCAGACTGGGG[A/G]CTTACAGCCTCAGCC | 7409 |
rs755008421 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840128 | AGCAACCACCTATTC[A/C]CCTCTCCCAGCCCCT | 7409 |
rs755014839 | snp | A/G | 2.03556e-05 | 0.0031902 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772783 | GCTGCGAGGGTGCAC[A/G]GCCGGCCCTGGGCAG | 7409 |
rs755044049 | snp | A/C | 1.64773e-05 | 0.00287026 | intron-variant | VAV1 | GRCh38.p7 | 19:6836949 | TTATGGATCCTATAA[A/C]CTCTCTGTTCCTGTT | 7409 |
rs755051674 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796112 | TGATCTAATCACCTC[C/T]TAAAGGTCCCGCTTC | 7409 |
rs755060773 | snp | A/G | 1.86827e-05 | 0.0030563 | intron-variant | VAV1 | GRCh38.p7 | 19:6832251 | GAGGGGCAGGGGCTG[A/G]GAAGGAGGAACGTGA | 7409 |
rs755075408 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773440 | GGAGCCTCCGCCAAC[A/G]TCTTCCCCCACATGT | 7409 |
rs755080325 | snp | C/T | 3.31686e-05 | 0.00407225 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6832189 | GTGGATGGAGCAGTT[C/T]GAGATGGCCATGTGA | 7409 |
rs755131190 | snp | C/T | 5.54185e-05 | 0.00526367 | intron-variant | VAV1 | GRCh38.p7 | 19:6826602 | CTGGTGGCCTGTCTT[C/T]TCCCTGTAGGTTCCT | 7409 |
rs755139300 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785237 | AGTGCAGTGGTGTTA[C/T]CATAGCTCACTGCAG | 7409 |
rs755151686 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812532 | GGGCATGGTGGTGGG[C/T]GCCTGTAATCCCAGC | 7409 |
rs755172769 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6821321 | CAGGAGAATCGCTTG[A/T]ACCTGGGAGGTGGAG | 7409 |
rs755209928 | snp | C/G | 1.65608e-05 | 0.00287752 | intron-variant | VAV1 | GRCh38.p7 | 19:6850662 | GCCCGGTGACCATCT[C/G]GTTCCAGATATAACG | 7409 |
rs755301733 | snp | A/G | 1.65225e-05 | 0.00287419 | intron-variant | VAV1 | GRCh38.p7 | 19:6833632 | ATGGGCAAGGTACGA[A/G]TGGGAGGGAGGCTGG | 7409 |
rs755316138 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844704 | ATCGTGCTCTCCTGC[A/G]TTAGCGCTCCTTCCG | 7409 |
rs755324877 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795232 | CCTATCTAGGAGCAG[A/G]GTGCAAAGGAGCCTG | 7409 |
rs755333060 | snp | C/T | 1.64963e-05 | 0.00287192 | missense | VAV1 | GRCh38.p7 | 19:6821641 | TCTACACCCTGTCTG[C/T]TCTGTCCTGGACCCC | 7409 |
rs755335843 | snp | A/C/G | 4.95179e-05 | 0.00497563 | missense | VAV1 | GRCh38.p7 | 19:6850750 | AAAAGGCTTTCCGGG[A/C/G]GCTTACGGTAAGGGT | 7409 |
rs755352544 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831461 | GGATTACAGGTGCCC[A/G]CCACCACGCCCAGCT | 7409 |
rs755352831 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832407 | TTCAGTTACCAGCCC[A/G]GACTCTTCTCCTTTC | 7409 |
rs755449782 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807237 | CATATAATGAAATAA[A/G]TATACAACTCACCAT | 7409 |
rs755460358 | snp | C/G/T | 0.000164748 | 0.00907474 | intron-variant | VAV1 | GRCh38.p7 | 19:6833706 | TTTCCTTTACCCTCC[C/G/T]GTAGATTTCCCAGGA | 7409 |
rs755481100 | snp | G/T | 1.65954e-05 | 0.00288053 | missense | VAV1 | GRCh38.p7 | 19:6828895 | ACGGCGCTCCAAGAT[G/T]GACAGGTGGGTGGAG | 7409 |
rs755506241 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843455 | ATGGTAATGACAGTT[A/C]CAGTTGTTTTTGTAG | 7409 |
rs755609796 | snp | C/T | 1.6588e-05 | 0.00287988 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825305 | TCCCTCCGAGTAGGA[C/T]CTGCTTCGTGTTCAT | 7409 |
rs755613485 | snp | A/G | 6.6177e-05 | 0.00575188 | intron-variant | VAV1 | GRCh38.p7 | 19:6773041 | GGCAGGTGTGCTGAG[A/G]GTTGGAGACGGGGGT | 7409 |
rs755674759 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818506 | CCTCAGGACCATTGC[A/G]TGCACTGTTCTCTCT | 7409 |
rs755742776 | snp | A/G | 4.9629e-05 | 0.00498117 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848079 | CTTGGTGCGGCAGAG[A/G]GTGAAGGATGCAGCA | 7409 |
rs755778761 | snp | A/G | 1.65751e-05 | 0.00287876 | intron-variant | VAV1 | GRCh38.p7 | 19:6833296 | CTTAGGTGAGAATCT[A/G]GGAGGAGGGTCCTGC | 7409 |
rs755829677 | snp | G/T | 1.65296e-05 | 0.00287481 | missense | VAV1 | GRCh38.p7 | 19:6828426 | TCTCTCAGGAGCTGG[G/T]GAAACACACGCAGGA | 7409 |
rs755831832 | snp | C/T | 1.77839e-05 | 0.00298189 | intron-variant | VAV1 | GRCh38.p7 | 19:6833503 | AAGGTCACTCGCTCT[C/T]CTTTATGTGTTCCCT | 7409 |
rs755852823 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791577 | CCCCATCTCAAGATC[C/T]TTACCTTACATCTTA | 7409 |
rs755872267 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837156 | TGGGGAGGGGGCTGC[C/T]CATCATGGCAGGTCT | 7409 |
rs755884049 | snp | C/T | 1.73791e-05 | 0.00294775 | intron-variant | VAV1 | GRCh38.p7 | 19:6853112 | GGGGGCTTACAGCCT[C/T]AGCCCCTTCCCATTG | 7409 |
rs755895062 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827564 | CAGGCCTGAGCAATC[A/G]TGCCCAGCCTCTTCC | 7409 |
rs755898713 | snp | C/T | 4.52622e-05 | 0.004757 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822284 | GGAGGCGGAAGGCGA[C/T]GAGATCTATGAGGAC | 7409 |
rs755904919 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855841 | ATCTATCTATCTATC[-/CATC]TATCCATTCATTATC | 7409 |
rs755905909 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790774 | TCCCGTTTTAATTAT[A/G]TGCAAATCAAGGGGT | 7409 |
rs755947869 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839747 | CCCAGGCTGGAGTGC[A/G]ATGGTGCAATCTTGG | 7409 |
rs755957302 | snp | C/T | 1.64977e-05 | 0.00287203 | intron-variant | VAV1 | GRCh38.p7 | 19:6828536 | CTGCAGACACCCTCC[C/T]GGTAGGGGCTGATCC | 7409 |
rs755970682 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812377 | TTTCAAAAATTGACC[A/G]GGTGCAGTGGTTCAC | 7409 |
rs755997487 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839312 | TCTCATAGAACATCC[C/T]TCTCTTTTTTCTTTT | 7409 |
rs756006907 | snp | A/G | 0.00034591 | 0.0131467 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6854020 | CCGATCAGAGCTGTC[A/G]CTCAAGGAGGGTGAC | 7409 |
rs756024601 | snp | C/T | 3.29777e-05 | 0.00406051 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828687 | ACAGATCACCAATTT[C/T]CAGCTGTCCATTGAG | 7409 |
rs756041810 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806288 | AACGGGGTTTCACCA[C/T]GTTGGTCTGGCTGGT | 7409 |
rs756073520 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831996 | TAGAGACTGTCATGG[A/G]CTTGCCTGTTCCCTA | 7409 |
rs756111890 | snp | A/G | 0.000104641 | 0.00723253 | intron-variant | VAV1 | GRCh38.p7 | 19:6822370 | GGGGAGGGCGTGGGC[A/G]GGGGGCAGCCCCAGG | 7409 |
rs756158157 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818364 | GGCTTAAACAGCAGA[A/G]ATTTATCTTCTCACA | 7409 |
rs756166968 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811582 | AAGAGATATTGGAGA[C/T]GGGCCTTGAAGGATG | 7409 |
rs756168720 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852440 | AAAGAACCTGTTTTT[C/G]GCCGGGCACGGTGGC | 7409 |
rs756178462 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784162 | AGGAAGTTGAGGCAG[C/G]AGGATCGCTTGAGCC | 7409 |
rs756182533 | snp | A/C/T | 0.00555928 | 0.0524292 | intron-variant | VAV1 | GRCh38.p7 | 19:6833169 | TTTTTTTTTTTTTTA[A/C/T]TTTTCCCCTGCCAGC | 7409 |
rs756202184 | snp | A/G | 4.9436e-05 | 0.00497148 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828105 | AGCCAACAACGGGAG[A/G]TTCACCCTGCGGGAC | 7409 |
rs756302359 | snp | A/T | 1.64751e-05 | 0.00287007 | missense | VAV1 | GRCh38.p7 | 19:6833711 | TTTACCCTCCCGTAG[A/T]TTTCCCAGGAACTAT | 7409 |
rs756313086 | snp | A/G/T | 7.1419e-05 | 0.0059754 | intron-variant | VAV1 | GRCh38.p7 | 19:6832241 | TCTGTCCACAGAGGG[A/G/T]CAGGGGCTGGGAAGG | 7409 |
rs756366518 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843415 | GATGATGACAATGAT[A/G]ATGATGATAATGATG | 7409 |
rs756371953 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806182 | ACCTCCGCCACCCGG[A/G]TTCAAGCAATTCTCC | 7409 |
rs756389839 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807145 | TCCATGGACCAGAGT[G/T]AGGGGGGATGGTTTC | 7409 |
rs756445171 | snp | A/C | 3.35312e-05 | 0.00409444 | intron-variant | VAV1 | GRCh38.p7 | 19:6821873 | GAGTGAGTGCTCAGG[A/C]CTGTGGCCGCACAGC | 7409 |
rs756460218 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813167 | CTTTAGGGTTTCTAA[C/T]GAGGTTGCACACAGA | 7409 |
rs756471564 | snp | A/G | 1.64779e-05 | 0.00287031 | intron-variant | VAV1 | GRCh38.p7 | 19:6833777 | TACCACAAATAATGG[A/G]CAACAGCGCGGGGAG | 7409 |
rs756491277 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842766 | TTGAACCTGGGAGAT[C/T]GAGGCTGCAGTGAGC | 7409 |
rs756531621 | in-del | -/C | 1.64997e-05 | 0.00287221 | intron-variant | VAV1 | GRCh38.p7 | 19:6828610 | CCAGGTTCACCCCTG[-/C]CCCCTCCCCAGGACC | 7409 |
rs756581644 | in-del | -/TAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838440 | ATCCATCCATCCATC[-/TAT]CATCTATCTACTTAT | 7409 |
rs756584664 | snp | A/G | 1.65002e-05 | 0.00287225 | intron-variant | VAV1 | GRCh38.p7 | 19:6829957 | TGGGGTCCTCCACGC[A/G]GTCGGCAGCTTAGCC | 7409 |
rs756598154 | snp | C/G/T | 4.94176e-05 | 0.00497059 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6829846 | GGGAGACTCCTATGA[C/G/T]CTCAAGGACTTTGTA | 7409 |
rs756621926 | in-del | -/C | 1.65759e-05 | 0.00287883 | frameshift-variant | VAV1 | GRCh38.p7 | 19:6836437 | TGTCCTCCAGGTCTG[-/C]CCAAGATGGAGGTGT | 7409 |
rs756632423 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845189 | GTTCAAGACCAGCCT[-/G]GGGCAACATGGTGAA | 7409 |
rs756654765 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833435 | TCTCCTGATCTAAAG[A/C]GAACCCAAGGGGTCC | 7409 |
rs756663372 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814371 | CTACCTTCCCTCTTG[C/T]TCCGGAAGCAACCAC | 7409 |
rs756681870 | in-del | -/GGCCG | 0.000122752 | 0.00783333 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772782 | GCTGCGAGGGTGCAC[-/GGCCG]GGCCGGCCCTGGGCA | 7409 |
rs756690633 | snp | C/T | 1.76627e-05 | 0.00297171 | intron-variant | VAV1 | GRCh38.p7 | 19:6833517 | TTCTTTATGTGTTCC[C/T]TGCATCTCAGAGGTA | 7409 |
rs756718419 | in-del | -/AAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780121 | TCTTAAAATAATAAT[-/AAT]AATAATAATAATAAT | 7409 |
rs756725254 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816824 | CAAAAATCAGCTGGA[C/T]GTGGTGGCACACTCC | 7409 |
rs756731520 | snp | A/G | 5.01861e-05 | 0.00500905 | intron-variant | VAV1 | GRCh38.p7 | 19:6850646 | GGTCCCCAGACTCAG[A/G]GCCCGGTGACCATCT | 7409 |
rs756756224 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778164 | CTGGTCTCGAACTCC[C/T]GACCTTAAGTGACCC | 7409 |
rs756764235 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827510 | AAACTCCTGGGCTCA[A/G]GCGACTCACCCACTC | 7409 |
rs756768032 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790391 | GTAACAAAGAACCAC[G/T]GATCGGATGTCTTAG | 7409 |
rs756791530 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776447 | CCATCCATCCATCCA[C/T]CCACCCATCCACCCA | 7409 |
rs756809044 | in-del | -/A | 1.68883e-05 | 0.00290584 | intron-variant | VAV1 | GRCh38.p7 | 19:6852939 | GCCCGCTGGGATAGC[-/A]ATCTGCCATGTGGTC | 7409 |
rs756885624 | snp | C/T | 3.31642e-05 | 0.00407198 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833609 | GAGGGTCCCTCCATG[C/T]GGCCGACATGGGCAA | 7409 |
rs756894641 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801398 | CCTGACCCTCCCACC[A/G]GTGCTGAAAAGTGGA | 7409 |
rs756924987 | snp | C/T | 1.65026e-05 | 0.00287246 | intron-variant | VAV1 | GRCh38.p7 | 19:6828581 | GGTAGGAGCCTGGGT[C/T]GGCTGTTGGGGGGCC | 7409 |
rs756980492 | snp | C/T | 1.67795e-05 | 0.00289646 | intron-variant | VAV1 | GRCh38.p7 | 19:6854133 | GTGACGGGGAGGGCA[C/T]GGGGGTTGAGCTGGT | 7409 |
rs756992113 | snp | A/T | 1.64749e-05 | 0.00287005 | missense | VAV1 | GRCh38.p7 | 19:6854037 | TCAAGGAGGGTGACA[A/T]CATCAAGATCCTTAA | 7409 |
rs756999100 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770786 | GGGAGGCTGAGGCGG[A/G]AGGATCACTTGAGCC | 7409 |
rs757014068 | snp | A/G | 1.65111e-05 | 0.0028732 | missense | VAV1 | GRCh38.p7 | 19:6836524 | CTCAACCCTGGAGAC[A/G]TTGTGGAGCTCACGA | 7409 |
rs757022687 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799616 | TAACCCCCAGCCCCC[A/G]ACAGGCCCCAGTGTG | 7409 |
rs757072694 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851038 | TATGTATGTGTGTAT[A/G]TATGCATATATACAT | 7409 |
rs757106364 | snp | C/T | 7.02247e-05 | 0.00592515 | intron-variant | VAV1 | GRCh38.p7 | 19:6822382 | GGCGGGGGGCAGCCC[C/T]AGGCCCCCCAACACC | 7409 |
rs757146819 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | VAV1 | GRCh38.p7 | 19:6836979 | TTTTGTCTCCTGGGT[A/G]TTTAGGGCAGAAATA | 7409 |
rs757161303 | snp | A/T | 1.64773e-05 | 0.00287026 | intron-variant | VAV1 | GRCh38.p7 | 19:6825002 | TCTCTCTGAGACTGG[A/T]CTGGAGGAGGGAATC | 7409 |
rs757188070 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811454 | AGAGCCCAGCACAGG[C/T]GTCTTCGTTGTCAGG | 7409 |
rs757194183 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809571 | AAAAAAGAGTAGAGT[A/C]ATCAGAGAAGTCAGC | 7409 |
rs757201714 | snp | A/G | 1.65201e-05 | 0.00287398 | intron-variant | VAV1 | GRCh38.p7 | 19:6833135 | CAGCCATAAAAAGGA[A/G]TAAAATACTGACCTT | 7409 |
rs757209438 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840732 | ACTTCAGCCTCCTGA[A/G]TAGCTGGGACTACAG | 7409 |
rs757290260 | snp | C/T | 1.64871e-05 | 0.00287111 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772918 | ACTGGCCCAGGCCCT[C/T]CGGGATGGTGTCCTT | 7409 |
rs757297343 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843383 | GTTGGAAGGAAAATG[C/G]TTACAATGATGATGA | 7409 |
rs757315975 | snp | C/T | 1.67713e-05 | 0.00289575 | intron-variant | VAV1 | GRCh38.p7 | 19:6821780 | TGGCTCACACCCTCC[C/T]GACCCCCCAGGCCCT | 7409 |
rs757317714 | snp | A/G | 1.6656e-05 | 0.00288578 | intron-variant | VAV1 | GRCh38.p7 | 19:6828375 | CCTCCCCGCAGGGAG[A/G]AGGGGAGGGGCCCAG | 7409 |
rs757374344 | in-del | -/TTAAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853266 | ATATAATTTAATTAA[-/TTAAT]TTATTTATTTTTTGA | 7409 |
rs757378410 | snp | C/T | 1.69117e-05 | 0.00290785 | intron-variant | VAV1 | GRCh38.p7 | 19:6853091 | GCAGGTAGGAGGTCT[C/T]AGACTGGGGGCTTAC | 7409 |
rs757387335 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792930 | CCAAATGTCAACAGC[A/G]CTGAGACCGAGGGAC | 7409 |
rs757419378 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806085 | TGCCACCTGTTTTTG[C/T]AAATGAAGCTCTTTT | 7409 |
rs757422185 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779645 | GCGGGAGGATTGCTT[A/G]GGTACAGGAGTTAGA | 7409 |
rs757442541 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803813 | CAGGTGATCCAGCCA[C/T]GTCGGCCTCCCAAAG | 7409 |
rs757514705 | snp | G/T | 1.64768e-05 | 0.00287021 | intron-variant | VAV1 | GRCh38.p7 | 19:6833858 | TAAGGGGGCCTACAA[G/T]CCCCCAGGCTGGGCA | 7409 |
rs757518626 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814005 | GTCAAGGTTACAGTG[A/C]ACTATGATCGTGCCA | 7409 |
rs757565996 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775184 | GCCACAGCCCATCCC[A/G]GCTTTGCCTACATTT | 7409 |
rs757570229 | snp | A/G | 1.64836e-05 | 0.0028708 | intron-variant | VAV1 | GRCh38.p7 | 19:6833982 | GGTTGCTGTGTGGGG[A/G]CAGGAGGAAAATTCA | 7409 |
rs757570479 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | VAV1 | GRCh38.p7 | 19:6829868 | GACTTTGTAAACCTG[C/T]ACAGCTTCCAGGTTC | 7409 |
rs757588302 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798540 | TGCCTGTAGTCCCAG[C/T]TACTTGGGAGGCTGA | 7409 |
rs757607691 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798044 | CACTTTGGGAGGCCG[A/C]GGTGGGCAAATCACT | 7409 |
rs757649108 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851076 | TATGTATGTGTATTT[-/A]AATTTTACTTACGTA | 7409 |
rs757684581 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773324 | GCCCCCAGATGGGAC[C/T]AACCAGAGGTCTCGG | 7409 |
rs757694132 | in-del | -/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771791 | AGAAAGGAAAGAAAG[-/G]AAAGGAAGGAAGGAA | 7409 |
rs757708446 | in-del | -/G | 0.000223914 | 0.0105786 | intron-variant | VAV1 | GRCh38.p7 | 19:6826762 | TCCTCCCCAGGCCCT[-/G]GGGGGCAGCAGGGAG | 7409 |
rs757724763 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794365 | GAAAACCAGGCCAGG[C/T]GTGGTGGCCCATGCC | 7409 |
rs757738282 | snp | A/C | 1.91499e-05 | 0.00309429 | intron-variant | VAV1 | GRCh38.p7 | 19:6825412 | ACAAGGAGAGGTGAG[A/C]CCCAGCTGGCCAGAC | 7409 |
rs757763063 | snp | C/T | 1.65143e-05 | 0.00287348 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848109 | AGAATTTGCCATCAG[C/T]ATTAAGTAACTCCTT | 7409 |
rs757767348 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823473 | TTTAAAGATATATAT[A/G]TAAAGTATGTATAAG | 7409 |
rs757812424 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796869 | CTTGAGGGCAGAGAT[G/T]CTTATCTCTTTGGTT | 7409 |
rs757842915 | snp | A/G | 1.64939e-05 | 0.0028717 | intron-variant | VAV1 | GRCh38.p7 | 19:6828736 | AGCCGGGTGGGCCAG[A/G]GGTGTGGCCACGTGG | 7409 |
rs757844799 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787993 | GAGGCAGGAGAATGG[C/T]GTGAACCTGGGAGGT | 7409 |
rs757852816 | snp | A/G | 0.000101175 | 0.00711178 | missense | VAV1 | GRCh38.p7 | 19:6825373 | CCCCTGGCGCAGCCA[A/G]TCTCTACCAGGTCTT | 7409 |
rs757904256 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799517 | TGCAGGTTTGTTACA[C/T]AGGTATACACGTGCC | 7409 |
rs757959034 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811331 | ATCAGCCTCCACACC[A/C]AGCCTCATTTATTTA | 7409 |
rs757968281 | in-del | -/C | 8.25887e-05 | 0.00642554 | intron-variant | VAV1 | GRCh38.p7 | 19:6848121 | CAGCATTAAGTAACT[-/C]CTTTCTCCCTGACTC | 7409 |
rs757973890 | snp | C/G | 1.65143e-05 | 0.00287348 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828871 | GGAACTCAAGATCAC[C/G]TCGGTGGAACGGCGC | 7409 |
rs757990991 | in-del | -/TTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788357 | CTTTTTATTTTATTA[-/TTA]TTATTATTATTATTA | 7409 |
rs758033864 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837795 | AAGTGAGTTTGCAGA[C/T]GACGTTCCCCTTTAC | 7409 |
rs758056579 | snp | A/G | 1.65217e-05 | 0.00287412 | intron-variant | VAV1 | GRCh38.p7 | 19:6857008 | GTGGAGGGGCAGTAG[A/G]AGGATGTGCAGAGGT | 7409 |
rs758091019 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850855 | CCCACATTCAGGGTG[A/G]CCCCCCTCCAGTGGC | 7409 |
rs758100170 | snp | G/T | 1.64738e-05 | 0.00286995 | intron-variant | VAV1 | GRCh38.p7 | 19:6843131 | TCTCTCTCTGTATTC[G/T]TAGGGCCCTCCTCAG | 7409 |
rs758131236 | snp | C/T | 3.29457e-05 | 0.00405854 | intron-variant, missense | VAV1 | GRCh38.p7 | 19:6837001 | GCAGAAATACATCTA[C/T]TAATGAAATTGGCTG | 7409 |
rs758164117 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810617 | GGCTGAGGCTGGAGA[A/G]TTGCTTGAACCCAGG | 7409 |
rs758179488 | snp | C/G | 1.6557e-05 | 0.00287719 | utr-variant-3-prime, missense | VAV1 | GRCh38.p7 | 19:6857144 | GACGAGAAACTCCAG[C/G]CTCTGAGCCCGGCGT | 7409 |
rs758179776 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782089 | TAATCCCAGCACTTC[A/G]GGAGGCTGAGGTGGG | 7409 |
rs758201706 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772933 | CCGGGATGGTGTCCT[C/T]CTGTGTCAGCTGCTT | 7409 |
rs758208990 | in-del | -/TC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789259 | TTCTCTCTCCTTTCT[-/TC]TTTTTTTTTTTTGAC | 7409 |
rs758223061 | snp | C/T | 0.000118877 | 0.00770871 | intron-variant | VAV1 | GRCh38.p7 | 19:6833171 | TTTTTTTTTTTTAAT[C/T]TTCCCCTGCCAGCTC | 7409 |
rs758273207 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819022 | TCAGGAGGCTGAGAC[A/G]GGAGAATTGCTTGAA | 7409 |
rs758276149 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773121 | GCCTGCAAAGGAGAG[C/G]GAATATGCTTACAGG | 7409 |
rs758311155 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771035 | AGGTGCCAGTAATCC[C/T]AGCTGCCTGGGAGGC | 7409 |
rs758328439 | snp | A/G | 4.95585e-05 | 0.00497763 | intron-variant | VAV1 | GRCh38.p7 | 19:6773025 | AGGTGAGCCCTCCGC[A/G]GGCAGGTGTGCTGAG | 7409 |
rs758350882 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819347 | CTTTGTGATGTGCTG[-/T]TTCATATCACAGAAT | 7409 |
rs758364316 | snp | A/C | 1.65111e-05 | 0.0028732 | missense | VAV1 | GRCh38.p7 | 19:6833249 | TGTTCTCCTTTGAGG[A/C]GACCACATCCTGCAA | 7409 |
rs758365316 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794741 | TTAGGTTATTAGTTA[C/T]TGCTGTGAAACAAAC | 7409 |
rs758372142 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842589 | TTTGGGAGGACAAGG[C/T]AGGAGGATTGCTTGA | 7409 |
rs758380804 | snp | C/G | 1.66452e-05 | 0.00288484 | intron-variant | VAV1 | GRCh38.p7 | 19:6853941 | ACTTCTGTTCTCTCT[C/G]CACAGTGGGAAGCAC | 7409 |
rs758497118 | snp | C/T | 8.25362e-05 | 0.00642349 | missense | VAV1 | GRCh38.p7 | 19:6836498 | CTGGAGCCATTGGAC[C/T]CTTTCTACGGCTCAA | 7409 |
rs758500473 | in-del | -/TC/TCTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838224 | TCTATTATCTATCTA[-/TC/TCTC]TATCATCATCATCAT | 7409 |
rs758507734 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827708 | GGTTCAAGCAATTCT[C/T]CTGCCTCAGTCTCCT | 7409 |
rs758601044 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854383 | GAATGTGGAGGACAG[A/C]CCTATAACCAAGCAG | 7409 |
rs758695911 | snp | A/G | 1.64871e-05 | 0.00287111 | missense | VAV1 | GRCh38.p7 | 19:6832133 | GACCAAGGTGCCCAG[A/G]GCTATGAGCTGTTCT | 7409 |
rs758742779 | snp | C/T | 1.65225e-05 | 0.00287419 | intron-variant | VAV1 | GRCh38.p7 | 19:6848126 | TTAAGTAACTCCTTT[C/T]TCCCTGACTCATACC | 7409 |
rs758873754 | snp | A/G | 8.83587e-05 | 0.00664617 | missense | VAV1 | GRCh38.p7 | 19:6826694 | GCAGCCCGGGAGGAC[A/G]TGCAGATGAAGCTGG | 7409 |
rs758911601 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808361 | CTCTCCTCCCCAATA[A/G]TTACCTTAGGACAAC | 7409 |
rs758924349 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779933 | TGGCTAACACGGTGA[A/G]ACCCCGTCTCTACTA | 7409 |
rs758932955 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833458 | AGGGGTCCCTTTATG[C/T]TTTTAGCAGAATATT | 7409 |
rs758979637 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811208 | GCCCGGCTAATTTTT[C/G]TATTTTTAGTAGAGA | 7409 |
rs759006907 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853317 | GTTGCCTAAGCTGGA[A/G]TGCAGTGGTGCGATC | 7409 |
rs759048210 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826862 | GAGGTACTAGCCAGC[A/C]AAGCAGAGGAAATGG | 7409 |
rs759072363 | snp | A/G | 1.64735e-05 | 0.00286993 | intron-variant | VAV1 | GRCh38.p7 | 19:6833956 | AGGAATGAGCTGGGT[A/G]AGTTGGCAGGGGTTG | 7409 |
rs759100574 | snp | A/C | 3.34202e-05 | 0.00408766 | intron-variant | VAV1 | GRCh38.p7 | 19:6850648 | TCCCCAGACTCAGGG[A/C]CCGGTGACCATCTGG | 7409 |
rs759136099 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793658 | TTTGTATGATAACAT[C/T]AAGTTTGCTTTGATA | 7409 |
rs759203826 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830856 | ACTTTGGGAGGCCGA[A/G]GTGGGAGAATTGCTT | 7409 |
rs759206485 | snp | A/C | 3.34236e-05 | 0.00408787 | intron-variant | VAV1 | GRCh38.p7 | 19:6825287 | GGTCCCAGCCCTCAC[A/C]CTTCCCTCCGAGTAG | 7409 |
rs759220633 | snp | C/T | 1.65649e-05 | 0.00287788 | intron-variant | VAV1 | GRCh38.p7 | 19:6832084 | TCTGAGCTCTGCTTC[C/T]CTGCAGTGGAGCCAC | 7409 |
rs759340736 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797651 | GAGGTTGTTGTGAGC[C/T]GAGATCGTGCCATTG | 7409 |
rs759359364 | in-del | -/CTCCGCGGGCAGGTGTG | 1.65111e-05 | 0.0028732 | intron-variant | VAV1 | GRCh38.p7 | 19:6773019 | TGTCCCAGGTGAGCC[-/CTCCGCGGGCAGGTGTG]CTGAGGGTTGGAGAC | 7409 |
rs759373425 | snp | A/G | 1.64936e-05 | 0.00287168 | intron-variant | VAV1 | GRCh38.p7 | 19:6821587 | GCCGTGGGGGTGTAC[A/G]AGGGGCTCACTGAGT | 7409 |
rs759384624 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814893 | CTAGGTTTTCTGAAG[A/G]CCTTCTTTATCAGGT | 7409 |
rs759398094 | in-del | -/TCTATCTC/TCTC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838333 | CTATCTATCTATCTA[-/TCTATCTC/TCTC]TATGTCTATCTATCC | 7409 |
rs759398960 | snp | A/G | 3.32508e-05 | 0.00407729 | missense | VAV1 | GRCh38.p7 | 19:6848056 | GCCAACCGCTCGGAC[A/G]GGACTTTCTTGGTGC | 7409 |
rs759434676 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803453 | GCTTCTGCTCCAGCC[C/G]TGTTTTAGCTAGTCC | 7409 |
rs759437644 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824888 | GGTTGTTTCCGCTTT[G/T]GGGTTATTATGAATA | 7409 |
rs759450110 | snp | G/T | 3.57373e-05 | 0.00422698 | intron-variant | VAV1 | GRCh38.p7 | 19:6833491 | GCCCTGTCTGTAAAG[G/T]TCACTCGCTCTTCTT | 7409 |
rs759467195 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774768 | TATCTTATCTTTTAT[G/T]TTTTGAGATGGAGTC | 7409 |
rs759469226 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837968 | ATCAAAAATTTTTTT[-/G]TTCCTATGGTTTCTC | 7409 |
rs759478082 | snp | C/T | 4.5208e-05 | 0.00475415 | intron-variant | VAV1 | GRCh38.p7 | 19:6822541 | CCACCCAGCGCCTGC[C/T]GGGCGCATGCGCGGG | 7409 |
rs759500816 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813745 | CAATTTTGGAGAGAA[C/T]TGAAGATTTTAAAAC | 7409 |
rs759533154 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815141 | TACAGTTGCTTCTTC[C/T]TTTATTTATTTATTT | 7409 |
rs759538564 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833152 | AAAATACTGACCTTC[-/TT]TTTTTTTTTTTTTTA | 7409 |
rs759550429 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779027 | GACTACAGGTGTGCA[C/T]CGGCATACCTGGGTG | 7409 |
rs759555901 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824089 | GCCACGGGTGCATGC[C/T]ACCACACCCTGCTTA | 7409 |
rs759577156 | snp | C/T | 1.68275e-05 | 0.0029006 | missense | VAV1 | GRCh38.p7 | 19:6833565 | CGCTGCCATCGGTGC[C/T]GGGCATCTGCACACA | 7409 |
rs759590161 | snp | C/T | 3.30606e-05 | 0.00406561 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772873 | GCCGCCCAGCCACCG[C/T]GTGACCTGGGATGGG | 7409 |
rs759607376 | snp | A/T | 3.29772e-05 | 0.00406048 | missense | VAV1 | GRCh38.p7 | 19:6857091 | ACGTGGAGGAAGATT[A/T]TTCTGAATACTGCTG | 7409 |
rs759636112 | snp | C/G | 1.6943e-05 | 0.00291053 | intron-variant | VAV1 | GRCh38.p7 | 19:6828932 | TGGATCTGGGATGGA[C/G]CCTGGGCAAAGGGGT | 7409 |
rs759657948 | snp | A/G | 3.30595e-05 | 0.00406554 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848085 | GCGGCAGAGGGTGAA[A/G]GATGCAGCAGAATTT | 7409 |
rs759660397 | snp | C/T | 1.65594e-05 | 0.0028774 | intron-variant | VAV1 | GRCh38.p7 | 19:6837101 | GGGTCCAGGGCGGGT[C/T]CTGGGAGGATGGACA | 7409 |
rs759684439 | in-del | -/TCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776191 | CCATCCATCCATCCA[-/TCC]ACTCCTCCATCCATC | 7409 |
rs759730093 | snp | A/G | 1.64836e-05 | 0.0028708 | missense | VAV1 | GRCh38.p7 | 19:6825075 | TGAAGCCCCTGCAAC[A/G]GTTCCTGAAACCTCA | 7409 |
rs759733938 | snp | C/G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834191 | AGGTCTTGCTACGTT[C/G/T]CCCAGCCATACTGTA | 7409 |
rs759741803 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796488 | GATCTCCTGGCTCCA[A/G]CATGCCAGGGCCTCA | 7409 |
rs759771157 | snp | A/C | 1.64972e-05 | 0.00287199 | missense | VAV1 | GRCh38.p7 | 19:6773010 | GCCCCCAGATGTCCC[A/C]GGTGAGCCCTCCGCG | 7409 |
rs759808290 | snp | A/G | 3.30781e-05 | 0.00406669 | missense | VAV1 | GRCh38.p7 | 19:6833216 | AGAATGCCACCGCCA[A/G]CGGGCATGACTTCCA | 7409 |
rs759832296 | snp | C/T | 1.74989e-05 | 0.00295789 | intron-variant | VAV1 | GRCh38.p7 | 19:6833163 | CTTCTTTTTTTTTTT[C/T]TTTTAATTTTCCCCT | 7409 |
rs759860276 | snp | A/T | 1.69195e-05 | 0.00290851 | intron-variant | VAV1 | GRCh38.p7 | 19:6828209 | TGGGCTCCACGTACC[A/T]ACTCTCCTGTGTCTA | 7409 |
rs759883753 | snp | C/G | 1.6483e-05 | 0.00287076 | missense | VAV1 | GRCh38.p7 | 19:6828085 | CCCCAGGAATGTTCT[C/G]AGAGAGCCAACAACG | 7409 |
rs759884791 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817493 | AGTTAACAAACATAT[A/G]TCAGGGGCCTCCTAC | 7409 |
rs759897130 | in-del | -/GTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827250 | CATTCCAGTGGGTTT[-/GTTT]GTTTGTTTGTTTGTT | 7409 |
rs759908306 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846297 | CTTATATAAAATTAT[A/G]TATTATGGGCTGGGC | 7409 |
rs759909334 | snp | C/G | 1.71882e-05 | 0.00293152 | intron-variant | VAV1 | GRCh38.p7 | 19:6852921 | TCTGCCCCCTTATGG[C/G]CTGGCCCGCTGGGAT | 7409 |
rs759934205 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791421 | CATCTCGAGGTCCTT[C/G]AGCTATCTCATCTCA | 7409 |
rs759937801 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827352 | AGCTCACCACAGCCT[A/C]GACCTCCTGGACTCA | 7409 |
rs759986829 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801965 | GCACAGTGGGTGCCC[C/G]CCTCTTCCTGGAGGA | 7409 |
rs760074232 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776456 | CATCCACCCACCCAT[C/T]CACCCACCCATCCAT | 7409 |
rs760094090 | snp | A/G | 1.64939e-05 | 0.0028717 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6853048 | GTTCCCCTTCAAGGA[A/G]CCTGAAAAGAGAACC | 7409 |
rs760124158 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818782 | GCTGTCTACTGAAAT[G/T]AGCCCTTAGAGGAAC | 7409 |
rs760145903 | snp | C/G/T | 3.35161e-05 | 0.00409355 | intron-variant | VAV1 | GRCh38.p7 | 19:6821869 | GATCGAGTGAGTGCT[C/G/T]AGGCCTGTGGCCGCA | 7409 |
rs760148080 | snp | C/T | 1.71507e-05 | 0.00292832 | intron-variant | VAV1 | GRCh38.p7 | 19:6832219 | AGTCCCCGTCTTCCT[C/T]CCTCTTTCTGTCCAC | 7409 |
rs760219042 | snp | A/G | 1.65102e-05 | 0.00287312 | missense | VAV1 | GRCh38.p7 | 19:6832100 | CTGCAGTGGAGCCAC[A/G]TGTTCCTCCTGATCG | 7409 |
rs760222375 | snp | A/G | 1.71737e-05 | 0.00293028 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825383 | AGCCAATCTCTACCA[A/G]GTCTTCATCAAATAC | 7409 |
rs760226013 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829307 | GCCAGGTTTCTAGAT[A/G]GGCAGTTGGGTGGAG | 7409 |
rs760289258 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843863 | TGAAATAGCTCTTGC[A/G]ATCCACAGTGTCCAT | 7409 |
rs760339335 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804935 | TCACCATGTTAGCCA[G/T]GATGGTCTCGATTGC | 7409 |
rs760343114 | snp | C/T | 0.000182432 | 0.00954896 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826636 | CTATGGCCGCTACTG[C/T]AGCCAGGTGGAGTCA | 7409 |
rs760345050 | snp | C/T | 1.64732e-05 | 0.0028699 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6820779 | GCGGAGCGAGCTCTT[C/T]GAAGCCTTTGACCTC | 7409 |
rs760353890 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842087 | CAAAATTAGCCGGGC[A/G]TGGTGACACACACCT | 7409 |
rs760544100 | snp | C/G | 1.66084e-05 | 0.00288165 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833600 | GTGTCTGGGGAGGGT[C/G]CCTCCATGTGGCCGA | 7409 |
rs760575809 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835523 | CACAGAAAGCTTTGT[C/T]AGAAAGCACTGCTAC | 7409 |
rs760614970 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785171 | GTTTCTCTTTCTCTC[C/T]CTCTCTGTCTTTTTT | 7409 |
rs760652758 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855677 | CCCATCTGTTAATCT[A/G]TCTCTATATTTATCC | 7409 |
rs760669490 | snp | G/T | 1.78589e-05 | 0.00298817 | intron-variant | VAV1 | GRCh38.p7 | 19:6847947 | CATATGGCAATATGG[G/T]GACCCAGGCACGGGG | 7409 |
rs760700904 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834058 | ACAGCCACATTGGGC[C/T]GGGTGCAATAGCTCA | 7409 |
rs760728557 | snp | C/G | 1.64787e-05 | 0.00287038 | intron-variant | VAV1 | GRCh38.p7 | 19:6828799 | ACCCTTGCTAGACCC[C/G]CTGCCTACTGCATAG | 7409 |
rs760749719 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845379 | AACAGAGCGAGACTC[A/G]GTCTCAAAAAATAAA | 7409 |
rs760769286 | snp | C/G | 0.000187172 | 0.00967217 | intron-variant | VAV1 | GRCh38.p7 | 19:6825173 | TAGTGCGGATAACCT[C/G]CTGCCCCTACCTCTC | 7409 |
rs760796877 | snp | A/G | 1.65323e-05 | 0.00287505 | missense | VAV1 | GRCh38.p7 | 19:6833218 | AATGCCACCGCCAAC[A/G]GGCATGACTTCCAGA | 7409 |
rs760861518 | snp | C/T | 1.71202e-05 | 0.00292572 | missense | VAV1 | GRCh38.p7 | 19:6848017 | GCAGGCCCCATGGAG[C/T]GGGCAGGGGCAGAGA | 7409 |
rs760874636 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844650 | GCAAAACCAGTTGCC[G/T]AGGTCTTAGAACACG | 7409 |
rs760904965 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791347 | AGGTCCTTGAGATAA[C/T]TCCTCATTTTGAGGT | 7409 |
rs760925972 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6828781 | TGGCTCCTTTCTTGG[-/G]AGACCCTTGCTAGAC | 7409 |
rs760967154 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850225 | TTGTTTGTTTCTTTG[-/T]TTTTTTTTTTTTTTT | 7409 |
rs760972545 | snp | C/T | 1.6501e-05 | 0.00287232 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828461 | ATGGAGAAGGAGAAC[C/T]TGCGGCTGGCCCTGG | 7409 |
rs760975682 | in-del | -/ATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838397 | TCAGTTCTTCTATCC[-/ATCC]ATCCATCCATCCATC | 7409 |
rs761012404 | snp | A/C | 5.4367e-05 | 0.0052135 | missense | VAV1 | GRCh38.p7 | 19:6822226 | CAACCCACAGCGACA[A/C]GGTGGAGGAGGATGA | 7409 |
rs761061867 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816637 | TAATCTCAAGCAGCA[A/T]CCCCACACCGATCTA | 7409 |
rs761065913 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827016 | ATTGTACCCCAAGTC[A/G]GGCTGAGCTCCCACT | 7409 |
rs761069445 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838642 | TATTCATTTATCATT[C/T]ATCCATCACCTGTCT | 7409 |
rs761088741 | snp | A/G | 1.65326e-05 | 0.00287507 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6853060 | GGAGCCTGAAAAGAG[A/G]ACCATCAGCAGGCCA | 7409 |
rs761169228 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839511 | GACCTCAAATGATCT[G/T]CCTGCCTCGGCCTCC | 7409 |
rs761190562 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826075 | AGGCGTGGTGGCTCA[C/T]GCCTGTAATTCCAGC | 7409 |
rs761213303 | snp | C/G | 3.37844e-05 | 0.00410987 | intron-variant | VAV1 | GRCh38.p7 | 19:6853914 | TGGGTATCTGCCCCA[C/G]ACCCTTTTCTCACTT | 7409 |
rs761222586 | snp | C/T | 5.34831e-05 | 0.00517095 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822317 | CATGCGCTCGGAGCC[C/T]GTGTCCATGCCGGTG | 7409 |
rs761250958 | snp | C/T | 3.31565e-05 | 0.0040715 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6836434 | CCCTGTCCTCCAGGT[C/T]TGCCCAAGATGGAGG | 7409 |
rs761381624 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791495 | TCCTCGTCTCAAGGT[C/T]CTTGAGATATCTCCT | 7409 |
rs761409372 | snp | A/G/T | 3.29692e-05 | 0.00406001 | missense | VAV1 | GRCh38.p7 | 19:6850723 | CAGAAGGACTGTACC[A/G/T]GATCACAGAGAAAAA | 7409 |
rs761423035 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820351 | GTGATCCACTCATCT[A/C]CGCCTCCTGAGTAGT | 7409 |
rs761453356 | snp | A/G | 3.29837e-05 | 0.00406088 | intron-variant | VAV1 | GRCh38.p7 | 19:6821615 | AGTGGCCACTGCCCC[A/G]TCACAGGTCATCTAC | 7409 |
rs761454725 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813504 | AGGAGCTATGGACCA[C/T]TGGGGGCCATCCTGG | 7409 |
rs761462726 | snp | A/C | 1.66371e-05 | 0.00288414 | intron-variant | VAV1 | GRCh38.p7 | 19:6850781 | CAATGTCCGCTCAAT[A/C]CCAGCTTTCCAGAAC | 7409 |
rs761489953 | snp | A/G | | | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772730 | GCTGTCGCTCCACAG[A/G]CGAGCAGGGCAGGCG | 7409 |
rs761500863 | snp | A/T | 3.29609e-05 | 0.00405948 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828823 | TGCATAGGACCAGTC[A/T]CTGGCTCACTATGGC | 7409 |
rs761505149 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843030 | TAATAGGCACTCACT[-/A]AATGCAAGTGGAATG | 7409 |
rs761512547 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855264 | TGTGGATAATTGCAT[C/T]GATGAGGAGTTTTGT | 7409 |
rs761576772 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833962 | GAGCTGGGTGAGTTG[A/G]CAGGGGTTGCTGTGT | 7409 |
rs761581551 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785038 | ATTGCTCTCTGCACC[A/G]CAGCCAAATCGGCCA | 7409 |
rs761657911 | snp | C/G | 1.64751e-05 | 0.00287007 | intron-variant | VAV1 | GRCh38.p7 | 19:6833749 | GTAAGACTTTCCCGT[C/G]GTCCTTCCTGTGTAC | 7409 |
rs761667232 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812531 | AGGGCATGGTGGTGG[A/G]CGCCTGTAATCCCAG | 7409 |
rs761709150 | snp | A/T | 1.65195e-05 | 0.00287393 | intron-variant | VAV1 | GRCh38.p7 | 19:6829736 | TGGTCAGAGGGCTGA[A/T]GGGGACAGTTGGGAA | 7409 |
rs761714540 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845246 | AAAAATTAGCTGGGC[A/C]TGGTGGCGCACGCCT | 7409 |
rs761717285 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772676 | CCACCCCCTCTCAGG[A/G]CGACAGTTACAGGCA | 7409 |
rs761755235 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | VAV1 | GRCh38.p7 | 19:6843113 | CTTTACACTAAGTTG[A/G]GGTCTCTCTCTGTAT | 7409 |
rs761759597 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795026 | TTCCCCACAACATGG[C/T]GACCGGGTTTCAAGA | 7409 |
rs761763104 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820895 | TGGGCAAGCTAAGGA[A/C]TGTCAGGGGACAGGC | 7409 |
rs761768326 | snp | C/G/T | 4.96137e-05 | 0.00498044 | utr-variant-3-prime, missense | VAV1 | GRCh38.p7 | 19:6857131 | GCCTTGGCAGAGAGA[C/G/T]GAGAAACTCCAGGCT | 7409 |
rs761775383 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831131 | TGGCTGTGGTAGGTG[A/G]GGGTGGGAGGGGGAG | 7409 |
rs761782853 | snp | C/T | 1.78896e-05 | 0.00299073 | intron-variant | VAV1 | GRCh38.p7 | 19:6833477 | TAGCAGAATATTTGG[C/T]CCTGTCTGTAAAGGT | 7409 |
rs761792837 | in-del | -/CT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816492 | AGCATCTCTCTCTCG[-/CT]CTCTCTCTCTCTCAC | 7409 |
rs761827709 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807752 | AATCCCAGCACTTTG[A/G]GAGGCCAAGGTGGGC | 7409 |
rs761882745 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817290 | GCTGGTTTTGAACTC[A/C]TGACCTCAAGTAATC | 7409 |
rs761920796 | snp | G/T | 1.65004e-05 | 0.00287227 | missense | VAV1 | GRCh38.p7 | 19:6828470 | GAGAACCTGCGGCTG[G/T]CCCTGGATGCCATGA | 7409 |
rs761921986 | in-del | -/C | 1.78469e-05 | 0.00298716 | intron-variant | VAV1 | GRCh38.p7 | 19:6833156 | ACTGACCTTCTTTTT[-/C]TTTTTTTTTTTAATT | 7409 |
rs761923260 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785153 | TTCTCTTATCTCCTT[C/T]AGGTTTCTCTTTCTC | 7409 |
rs761941077 | snp | A/G | 1.64735e-05 | 0.00286993 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6820749 | GTCCACCTGCTGTGA[A/G]AAGTTCGGCCTCAAG | 7409 |
rs761954450 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800607 | GAGCCACCACACCCA[A/G]CTTCTTTTTTTTGTT | 7409 |
rs761976173 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800187 | TCTTCCTTTGTGCTG[C/G]AATTGCAAGGTAAAA | 7409 |
rs761989004 | snp | A/C | 1.69395e-05 | 0.00291024 | missense | VAV1 | GRCh38.p7 | 19:6833557 | AGGGCTACCGCTGCC[A/C]TCGGTGCCGGGCATC | 7409 |
rs762034032 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818219 | GGGATTTTAAATAGG[G/T]TGGCTAGAGGAGGTC | 7409 |
rs762043748 | snp | C/T | 1.64996e-05 | 0.0028722 | intron-variant | VAV1 | GRCh38.p7 | 19:6828610 | CCAGGTTCACCCCTG[C/T]CCCCTCCCCAGGACC | 7409 |
rs762075395 | snp | G/T | 1.65586e-05 | 0.00287733 | intron-variant | VAV1 | GRCh38.p7 | 19:6854104 | CTATGGCCGGGTGAG[G/T]CAGGCAGGGCTGGGT | 7409 |
rs762100134 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6825985 | GAGGCGGAGGTTGCA[C/G]TGAGTCAAGATCATG | 7409 |
rs762115334 | in-del | -/TA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805750 | TCACACATATGTGTA[-/TA]TATATATATGCACAC | 7409 |
rs762152876 | snp | G/T | 1.66369e-05 | 0.00288412 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772758 | GCGTGCGGGCGGGTG[G/T]GTGGTGGAGGCTGCG | 7409 |
rs762233639 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799317 | GGACTACAGGTGTGC[A/G]CCACCACGCCTGGCT | 7409 |
rs762244089 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851404 | TCAGGCTGGCCTTGA[A/G]CTCCTGGGCTCAAAT | 7409 |
rs762270209 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837410 | TTGCCTGTGTCCTTG[C/T]CCTGCTCCTGGTGGA | 7409 |
rs762320983 | snp | C/T | 0.000181436 | 0.00952287 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6832114 | CATGTTCCTCCTGAT[C/T]GAGGACCAAGGTGCC | 7409 |
rs762340655 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819653 | GATGGATTTTAACCA[A/G]CTCTACTGACGAGTC | 7409 |
rs762350999 | in-del | -/AATA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853245 | TCCTATATATATTTT[-/AATA]TAATATAATTTAATT | 7409 |
rs762407953 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839564 | TGAGCCACCACGCCC[A/G]GCTGGGTATGGCATT | 7409 |
rs762442646 | snp | C/G | 0.000153732 | 0.00876597 | intron-variant | VAV1 | GRCh38.p7 | 19:6850808 | GAACCTAGGAGGACC[C/G]TCCCTGCACCTCCGC | 7409 |
rs762460951 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853785 | AGGATGATGCTGGGA[C/G]TACAATTGTGTCCCC | 7409 |
rs762482707 | snp | A/G/T | 0.000101162 | 0.0071114 | intron-variant | VAV1 | GRCh38.p7 | 19:6828204 | AGGCGTGGGCTCCAC[A/G/T]TACCTACTCTCCTGT | 7409 |
rs762496035 | snp | A/G | 1.64743e-05 | 0.00287 | intron-variant | VAV1 | GRCh38.p7 | 19:6833763 | TGGTCCTTCCTGTGT[A/G]CCACAAATAATGGGC | 7409 |
rs762504174 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840305 | CAGAATTTTCTTTCT[-/TT]TTTTTTTTTTTTTTG | 7409 |
rs762524614 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6852093 | ATCATAGCTCACTGT[A/G]GCTTCAAACCCCTGG | 7409 |
rs762526877 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783852 | GTTAAACTGGAGCTG[G/T]GGATAAAAAGGAGAT | 7409 |
rs762530546 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803837 | CCCAAAGTGCTGAGA[A/T]TACAGGTGTGAGCCA | 7409 |
rs762533090 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805937 | GGGTTTATGGGCTGA[C/T]TCCCTCAACTTCCTC | 7409 |
rs762582915 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851994 | GGTAGTGAGTATCTA[C/T]GAACCTTTCATATAG | 7409 |
rs762595879 | snp | A/G | 1.67024e-05 | 0.0028898 | intron-variant | VAV1 | GRCh38.p7 | 19:6825124 | TATCAACATTGAGGT[A/G]AGCCGGCCGATCCCC | 7409 |
rs762621714 | snp | G/T | 1.64741e-05 | 0.00286998 | missense | VAV1 | GRCh38.p7 | 19:6833943 | TCAGGACAAAAAGAG[G/T]AATGAGCTGGGTGAG | 7409 |
rs762626009 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784955 | ACAAAATCCTCACTG[C/T]AGCCCACAAGGGCTT | 7409 |
rs762655523 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843973 | CATCAGCTATTTAAT[A/G]AGCTCCTTTAATCTT | 7409 |
rs762657782 | in-del | -/AAGAAAGG | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771789 | GAAAGAAAGGAAAGA[-/AAGAAAGG]AAGGAAGGAAGGAAG | 7409 |
rs762661765 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820611 | GCTTTCATTTCCCCT[C/T]CACACCAGTCCCCAA | 7409 |
rs762746904 | snp | A/G | 1.64893e-05 | 0.0028713 | intron-variant | VAV1 | GRCh38.p7 | 19:6829943 | TGACGCCGGAACTAT[A/G]GGGTCCTCCACGCAG | 7409 |
rs762788926 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806691 | TCATTGGTCTGAAGT[A/G]GGTCATGTGTTAATC | 7409 |
rs762832668 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797215 | CCAGACTGGGTGACA[C/G]AGTGAGACTCAGTAT | 7409 |
rs762844656 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831889 | GTGTGTGCATGTGCA[C/T]GCCTGCGTATGTGGT | 7409 |
rs762865924 | in-del | -/AAAAA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778725 | GAGAGACTTTGTCTC[-/AAAAA]AAAAAACAAAACAAA | 7409 |
rs762871958 | snp | C/T | 1.68579e-05 | 0.00290321 | intron-variant | VAV1 | GRCh38.p7 | 19:6825263 | CTGGCCCCCTGAGCC[C/T]TGGGCTCTGGTCCCA | 7409 |
rs762880431 | snp | C/T | 1.64969e-05 | 0.00287196 | intron-variant | VAV1 | GRCh38.p7 | 19:6828614 | GTTCACCCCTGCCCC[C/T]TCCCCAGGACCTGGC | 7409 |
rs762902858 | snp | A/T | 7.1328e-05 | 0.00597151 | intron-variant | VAV1 | GRCh38.p7 | 19:6847957 | TATGGGGACCCAGGC[A/T]CGGGGACCGTGCCAC | 7409 |
rs762912510 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805814 | TTCATTTATATGAAT[A/C]AAAAAGAAACTAAAA | 7409 |
rs762931379 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843252 | GAACCTCCGAGCCAA[G/T]TAGTTATGCATTCTG | 7409 |
rs762937808 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775025 | ACCACCTCGGCCTCT[C/T]GAAAGGCTGGGATTA | 7409 |
rs762951697 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776226 | CTCATCCATTTATCC[A/G]TCCACTCATCTATCC | 7409 |
rs762960130 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856646 | GGAGAATCACTTGAA[C/T]CCGGGAGGTGGAGGT | 7409 |
rs762974066 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814112 | AAAACACTGAGTCTT[A/G]CTAGAAAGGAACTGG | 7409 |
rs762977130 | in-del | -/AAAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6822768 | CAGTCAAAAAACCAA[-/AAAC]AAACAAAATAAATAC | 7409 |
rs763007656 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824924 | ACTGTGAACATTCTT[G/T]TACAAGTTTTTGTGT | 7409 |
rs763007742 | snp | C/T | 3.43654e-05 | 0.00414506 | intron-variant | VAV1 | GRCh38.p7 | 19:6822348 | CGTGACGTGGAGGGT[C/T]GGGCCTGGGGAGGGC | 7409 |
rs763035405 | in-del | -/TAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846829 | TATATAATGATTATA[-/TAT]TATTATATATAACTA | 7409 |
rs763059084 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837133 | ACTTGGAAAGACACC[A/C]CCGGAGTTGGGGAGG | 7409 |
rs763133831 | snp | A/G | 4.18708e-05 | 0.00457533 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772775 | TGGTGGAGGCTGCGA[A/G]GGTGCACGGCCGGCC | 7409 |
rs763139145 | in-del | -/ATCCATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777243 | TTTAACTATCCATCC[-/ATCCATCC]ATCCATCCATCCATC | 7409 |
rs763157547 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | VAV1 | GRCh38.p7 | 19:6828787 | CTTTCTTGGGAGACC[C/T]TTGCTAGACCCCCTG | 7409 |
rs763182335 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803350 | GGTTGTCGGGTCATT[A/G]CCTTGGGAAAGGAGT | 7409 |
rs763208696 | snp | A/C | 1.86809e-05 | 0.00305616 | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6822509 | ACGCTGGGCTCCATC[A/C]AGCAGGTGGGCGCCT | 7409 |
rs763267007 | snp | C/T | 7.05517e-05 | 0.00593893 | intron-variant | VAV1 | GRCh38.p7 | 19:6833159 | TGACCTTCTTTTTTT[C/T]TTTTTTTTAATTTTC | 7409 |
rs763289472 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809423 | AGTATTTGTAATCTA[A/C]CACAAAGGGCATTCA | 7409 |
rs763298675 | in-del | -/CT | 1.68764e-05 | 0.00290481 | intron-variant | VAV1 | GRCh38.p7 | 19:6825256 | TTCCTTCCTGGCCCC[-/CT]GAGCCCTGGGCTCTG | 7409 |
rs763327327 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781384 | CTCTGCCGCCTCCCC[A/G]ACAGACGGTTCTGTT | 7409 |
rs763341409 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818194 | CCTGGGCTCAAGTCA[A/G]CCTGGGAGTGGGATT | 7409 |
rs763366547 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849998 | CTATTTTTAGTTCTT[C/T]GAGAAACCTCCAAAC | 7409 |
rs763415851 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830502 | TGGAATGCAGTGGCA[C/T]GGTCTTGGCTCACTG | 7409 |
rs763420126 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848270 | CCTTTCACCTTCTTT[A/C]TTTCTTTTAATTGAC | 7409 |
rs763490760 | snp | C/G | 1.74769e-05 | 0.00295603 | missense | VAV1 | GRCh38.p7 | 19:6825389 | TCTCTACCAGGTCTT[C/G]ATCAAATACAAGGAG | 7409 |
rs763556498 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790338 | GAGTTCATGCCCTCT[C/T]GAGGGAGGGGGTGGT | 7409 |
rs763573602 | snp | C/T | 1.65102e-05 | 0.00287312 | intron-variant | VAV1 | GRCh38.p7 | 19:6828054 | CCTGCCTCAGTTTCC[C/T]CATTGTTCTCTGATT | 7409 |
rs763607705 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818427 | TCTTCTTCCTCCTCG[C/T]CCACTCTAACTCCAG | 7409 |
rs763622630 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784987 | TGCATTTGGCCTCTG[G/T]CCATCTCTCAGCCCT | 7409 |
rs763653132 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812058 | ACAAATGCTCCTATT[C/G]TATTGGCCAGAAGCA | 7409 |
rs763684980 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853788 | ATGATGCTGGGAGTA[C/T]AATTGTGTCCCCTTA | 7409 |
rs763685123 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838995 | GCAACCTCCGCCTTC[C/T]GGTTTCAAGCGATTC | 7409 |
rs763699001 | snp | A/G | 1.64732e-05 | 0.0028699 | missense | VAV1 | GRCh38.p7 | 19:6820781 | GGAGCGAGCTCTTCG[A/G]AGCCTTTGACCTCTT | 7409 |
rs763750393 | snp | A/G | 1.64925e-05 | 0.00287158 | intron-variant | VAV1 | GRCh38.p7 | 19:6821599 | TACAAGGGGCTCACT[A/G]AGTGGCCACTGCCCC | 7409 |
rs763790618 | snp | C/G | 8.42297e-05 | 0.00648905 | intron-variant | VAV1 | GRCh38.p7 | 19:6850631 | GTGGGGAATGGGCCT[C/G]GTCCCCAGACTCAGG | 7409 |
rs763802344 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783041 | ATAAATTAGCCAGGC[A/G]TGGTGGTGTATGCCT | 7409 |
rs763819169 | snp | C/G/T | 4.94241e-05 | 0.00497092 | intron-variant | VAV1 | GRCh38.p7 | 19:6833680 | CTTTGGAGGATTTCC[C/G/T]GTTCTCACCATTTCC | 7409 |
rs763849108 | snp | C/T | 1.66026e-05 | 0.00288115 | missense | VAV1 | GRCh38.p7 | 19:6833602 | GTCTGGGGAGGGTCC[C/T]TCCATGTGGCCGACA | 7409 |
rs763883241 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794950 | GGGATGACTTGAGGC[C/T]ATGCTCAGTTGGGGC | 7409 |
rs763886100 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820637 | CCCAAGCTAGGTGGC[C/G]TGGGGGTCAGTTTCT | 7409 |
rs763901902 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783989 | CCAGGCATGGTGGCT[C/T]ATGCCTGTAATCTCA | 7409 |
rs763977600 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832877 | TAACAGCATTGTGCA[A/G]CCATCACCTCTATCC | 7409 |
rs763982826 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816317 | GAGCCACCATGCCCG[C/G]CTACAAAAACATTTT | 7409 |
rs764006033 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793846 | GAGATAAAACTAGTC[C/T]CTACCTTATAGGATT | 7409 |
rs764006686 | snp | C/T | 4.94947e-05 | 0.00497443 | intron-variant | VAV1 | GRCh38.p7 | 19:6828715 | GAGAACCTGGTGAGG[C/T]GGTGGAGCCGGGTGG | 7409 |
rs764009709 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806764 | TGACTGGAACTGGGG[C/G]TGGAGCCCCTCTCAG | 7409 |
rs764058907 | snp | G/T | 1.64754e-05 | 0.00287009 | intron-variant | VAV1 | GRCh38.p7 | 19:6836955 | ATCCTATAACCTCTC[G/T]GTTCCTGTTTTTGTC | 7409 |
rs764060162 | snp | C/T | 1.64787e-05 | 0.00287038 | intron-variant | VAV1 | GRCh38.p7 | 19:6828804 | TGCTAGACCCCCTGC[C/T]TACTGCATAGGACCA | 7409 |
rs764064348 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831993 | GCATAGAGACTGTCA[C/T]GGGCTTGCCTGTTCC | 7409 |
rs764140485 | snp | A/C | 1.64925e-05 | 0.00287158 | missense | VAV1 | GRCh38.p7 | 19:6857094 | TGGAGGAAGATTATT[A/C]TGAATACTGCTGAGC | 7409 |
rs764184305 | snp | A/G | 1.65288e-05 | 0.00287474 | missense | VAV1 | GRCh38.p7 | 19:6833219 | ATGCCACCGCCAACG[A/G]GCATGACTTCCAGAT | 7409 |
rs764188724 | snp | A/C | 0.000133182 | 0.00815926 | intron-variant | VAV1 | GRCh38.p7 | 19:6822545 | CCAGCGCCTGCCGGG[A/C]GCATGCGCGGGAGCT | 7409 |
rs764207188 | snp | A/T | | | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6852989 | GAGTTTTACCAGCAG[A/T]ACTCTCTAAAGGATT | 7409 |
rs764235143 | snp | A/G | 1.66613e-05 | 0.00288623 | intron-variant | VAV1 | GRCh38.p7 | 19:6828370 | AAGGCCCTCCCCGCA[A/G]GGAGAAGGGGAGGGG | 7409 |
rs764237284 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813871 | CCAGCCTGTGTGACA[C/T]AGTGACATCCTGTCT | 7409 |
rs764265307 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779331 | GTGCTGGGATTACAG[C/G]CATGAGCCACTGCAC | 7409 |
rs764266657 | in-del | -/TTT | 0.000108965 | 0.00738043 | intron-variant | VAV1 | GRCh38.p7 | 19:6833152 | AAAATACTGACCTTC[-/TTT]TTTTTTTTTTTTTAA | 7409 |
rs764279690 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824320 | TCTCTTATCTTCCCC[C/T]GGTCCATGGCAACCA | 7409 |
rs764281973 | snp | C/T | 1.6764e-05 | 0.00289512 | intron-variant | VAV1 | GRCh38.p7 | 19:6821874 | AGTGAGTGCTCAGGC[C/T]TGTGGCCGCACAGCT | 7409 |
rs764282670 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779262 | TTGCTATGATGCCCA[-/G]GCTGGTCTTGAACTC | 7409 |
rs764288298 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798168 | TATAATCCCAGCTAC[C/T]CAGGAGGTGGAGGCA | 7409 |
rs764341332 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800108 | TTTGAGACCAACCTG[A/C]CCGACATAGTGAGGC | 7409 |
rs764354477 | in-del | -/TCAC | 0.00015373 | 0.00876591 | intron-variant | VAV1 | GRCh38.p7 | 19:6825441 | ACTGAAGCTCTGGGG[-/TCAC]TCTGTCTTGCCTAGG | 7409 |
rs764359782 | snp | A/T | 1.64999e-05 | 0.00287222 | missense | VAV1 | GRCh38.p7 | 19:6828462 | TGGAGAAGGAGAACC[A/T]GCGGCTGGCCCTGGA | 7409 |
rs764414174 | in-del | -/GAA | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771791 | AAGAAAGGAAAGAAA[-/GAA]AGGAAGGAAGGAAGG | 7409 |
rs764458602 | snp | A/C | 0.000149949 | 0.00865748 | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6853077 | CCATCAGCAGGCCAG[A/C]AGGTAGGAGGTCTCA | 7409 |
rs764489679 | snp | C/G | 0.000154931 | 0.00880008 | missense | VAV1 | GRCh38.p7 | 19:6822233 | CAGCGACACGGTGGA[C/G]GAGGATGAGGACCTG | 7409 |
rs764522005 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836169 | ATGAGCCACCGTGCC[C/T]AGCCAGGACACATGT | 7409 |
rs764580249 | snp | C/T | 1.65081e-05 | 0.00287293 | missense | VAV1 | GRCh38.p7 | 19:6832101 | TGCAGTGGAGCCACA[C/T]GTTCCTCCTGATCGA | 7409 |
rs764583035 | snp | A/C | 1.6888e-05 | 0.00290581 | intron-variant | VAV1 | GRCh38.p7 | 19:6853916 | GGTATCTGCCCCAGA[A/C]CCTTTTCTCACTTCT | 7409 |
rs764604340 | snp | C/G | 1.65061e-05 | 0.00287277 | intron-variant | VAV1 | GRCh38.p7 | 19:6829960 | GGTCCTCCACGCAGT[C/G]GGCAGCTTAGCCCTC | 7409 |
rs764621143 | snp | C/T | 3.2987e-05 | 0.00406108 | missense | VAV1 | GRCh38.p7 | 19:6821628 | CCGTCACAGGTCATC[C/T]ACACCCTGTCTGCTC | 7409 |
rs764625433 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837661 | CTATGAGAATAATGC[A/G]AAGAGCTCCTGTGTA | 7409 |
rs764628921 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781568 | TATCACTTGCTTACT[A/G]TTGTTGCACTTTCTA | 7409 |
rs764661277 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809459 | GAGGCAACCTTATAT[A/G]TGAGACCTGGAGATG | 7409 |
rs764698956 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851741 | AATGATCTAAGGCAT[A/G]TGGTTTTTACCCATG | 7409 |
rs764749335 | in-del | -/TTTTTTTTTTTTTTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844064 | TTCTTCTTCTTCTTC[-/TTTTTTTTTTTTTTTT]TTTTTTTTTTTTTTT | 7409 |
rs764796084 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779349 | TGAGCCACTGCACCC[A/G]GCCAGAATAGAGGTT | 7409 |
rs764836003 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849658 | ACCCAATGTTTAACC[A/C]CTGCTTATAAGTGAG | 7409 |
rs764868084 | snp | C/T | 1.64743e-05 | 0.00287 | intron-variant | VAV1 | GRCh38.p7 | 19:6833753 | GACTTTCCCGTGGTC[C/T]TTCCTGTGTACCACA | 7409 |
rs764888832 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant | VAV1 | GRCh38.p7 | 19:6833688 | GATTTCCCGTTCTCA[C/G]CATTTCCTTTACCCT | 7409 |
rs764908345 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783790 | TTGTTATTGGCCAGA[A/G]CTTGGTCACATGGCT | 7409 |
rs764921092 | snp | G/T | 1.65135e-05 | 0.00287341 | intron-variant | VAV1 | GRCh38.p7 | 19:6829745 | GGCTGATGGGGACAG[G/T]TGGGAAGAGCCAGAC | 7409 |
rs764957793 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792776 | GAGTGACTCTGTCCT[C/T]CCAGGGGACATTTGG | 7409 |
rs765008044 | snp | C/G | 1.64819e-05 | 0.00287066 | missense | VAV1 | GRCh38.p7 | 19:6828827 | TAGGACCAGTCTCTG[C/G]CTCACTATGGCCGGC | 7409 |
rs765032856 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831781 | TCAGCAGGTGCTGCA[C/G]CAATGCTTTGTTGAA | 7409 |
rs765074663 | snp | C/G | 1.64738e-05 | 0.00286995 | intron-variant | VAV1 | GRCh38.p7 | 19:6843121 | TAAGTTGGGGTCTCT[C/G]TCTGTATTCTTAGGG | 7409 |
rs765093897 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805434 | CATCTCAAACAAAAC[A/G]AAACAAAACAAAAAC | 7409 |
rs765102579 | snp | C/T | 3.29538e-05 | 0.00405904 | intron-variant | VAV1 | GRCh38.p7 | 19:6825017 | TCTGGAGGAGGGAAT[C/T]TTATCTTCCGTCATC | 7409 |
rs765105830 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795849 | CCACCGCGCCCAGCT[A/G]ATTTTTGTTATTTTT | 7409 |
rs765156265 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815048 | TTGACAAAAAGAGAA[C/G]AGGTCTTGGGTCAGA | 7409 |
rs765156681 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856530 | AGTTTGAAACCAGCC[C/T]GGCCAACATGGTGAA | 7409 |
rs765157570 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830880 | ATTGCTTGAGCCCAG[A/G]AGTTTGAGATCAGCC | 7409 |
rs765183439 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786741 | TGAACCACGATTGCA[A/C]CACTGCACTCTAGCC | 7409 |
rs765195655 | in-del | -/TT/TTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785678 | TTTTTTTTTTTTTTG[-/TT/TTA]AGATAGAGTCTTGCT | 7409 |
rs765263357 | snp | C/T | 1.78669e-05 | 0.00298883 | intron-variant | VAV1 | GRCh38.p7 | 19:6847950 | ATGGCAATATGGGGA[C/T]CCAGGCACGGGGACC | 7409 |
rs765310816 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773469 | GTGTCTCCTCCTCCC[A/G]GGCCCTGGGCCCCTT | 7409 |
rs765331672 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824223 | TGGGATTTTGGGTGT[A/G]AGCCACCACCCCGGC | 7409 |
rs765336610 | snp | A/C | 1.64996e-05 | 0.0028722 | intron-variant | VAV1 | GRCh38.p7 | 19:6828611 | CAGGTTCACCCCTGC[A/C]CCCTCCCCAGGACCT | 7409 |
rs765341021 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855536 | ACCCTTCCACTCACG[C/G]ATCTATCTAACCATC | 7409 |
rs765360774 | snp | C/G | 3.34348e-05 | 0.00408855 | intron-variant | VAV1 | GRCh38.p7 | 19:6853932 | CCTTTTCTCACTTCT[C/G]TTCTCTCTCCACAGT | 7409 |
rs765365449 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786244 | GAATATATGATTCTA[A/G]TTGCTTCATTCATTC | 7409 |
rs765389170 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782432 | AAGGATTAAACATGA[C/T]AAGGTAAATGAAATT | 7409 |
rs765401527 | snp | A/G | 4.87698e-05 | 0.00493787 | missense | VAV1 | GRCh38.p7 | 19:6822243 | GTGGAGGAGGATGAG[A/G]ACCTGTATGACTGCG | 7409 |
rs765414911 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797438 | CCGGGCACAGTGGCT[C/G]ATGCCTGTAATCCCA | 7409 |
rs765490931 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846512 | AGAATTGCTTGAACC[C/T]AGGAGGCAGAGGTTG | 7409 |
rs765544129 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818019 | AAATGGGATCTCATT[A/G]TGTGGCCCCAGGCTG | 7409 |
rs765559688 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848184 | GGGAAAAAGGGTATC[C/T]AGGTTTTACTTTATA | 7409 |
rs765595068 | snp | C/T | 3.29924e-05 | 0.00406142 | intron-variant | VAV1 | GRCh38.p7 | 19:6828517 | GGTGCTGGTGACTCA[C/T]CTGCTGCAGACACCC | 7409 |
rs765597554 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809393 | GCAATTCTCTTTGGC[C/T]GGTAGGAGCTGGAAA | 7409 |
rs765599789 | snp | C/G | 1.65151e-05 | 0.00287355 | missense | VAV1 | GRCh38.p7 | 19:6836482 | GGGCTTCCTCCACCC[C/G]CTGGAGCCATTGGAC | 7409 |
rs765624250 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838436 | ATCCATCCATCCATC[-/C]ATCTATCATCTATCT | 7409 |
rs765624500 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800190 | TCCTTTGTGCTGGAA[C/T]TGCAAGGTAAAAAAA | 7409 |
rs765709658 | snp | G/T | 1.9983e-05 | 0.00316087 | intron-variant | VAV1 | GRCh38.p7 | 19:6825421 | GGTGAGACCCAGCTG[G/T]CCAGACTGAAGCTCT | 7409 |
rs765720226 | snp | A/G | 5.21173e-05 | 0.0051045 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826690 | GGCCGCAGCCCGGGA[A/G]GACGTGCAGATGAAG | 7409 |
rs765770275 | snp | A/G/T | 5.3393e-05 | 0.00516663 | intron-variant | VAV1 | GRCh38.p7 | 19:6832240 | TTCTGTCCACAGAGG[A/G/T]GCAGGGGCTGGGAAG | 7409 |
rs765856544 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783471 | CCATCACCTCCATCC[-/T]TTTTTTTTTTTTTTT | 7409 |
rs765885595 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830684 | ACCTCAAGTGACCTG[C/T]CCATCTTGGCCTCCC | 7409 |
rs765892882 | snp | C/G | 8.23689e-05 | 0.00641698 | intron-variant | VAV1 | GRCh38.p7 | 19:6833764 | GGTCCTTCCTGTGTA[C/G]CACAAATAATGGGCA | 7409 |
rs765990995 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805948 | CTGATTCCCTCAACT[A/T]CCTCCCGTCTAACAA | 7409 |
rs766012417 | in-del | -/GAAAG | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771791 | AAGAAAGGAAAGAAA[-/GAAAG]GAAGGAAGGAAGGAA | 7409 |
rs766029115 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850035 | CCGCAGTGGCTGAAC[C/G]AATTTACAGTCCAGC | 7409 |
rs766050948 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793551 | AGTGCTTATATAGTA[C/T]AGGAAAATGTGCAGG | 7409 |
rs766077182 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | VAV1 | GRCh38.p7 | 19:6829944 | GACGCCGGAACTATG[A/G]GGTCCTCCACGCAGT | 7409 |
rs766083058 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807668 | AGTGAGCTGTAATCA[C/T]GCCACTGCACTCAAC | 7409 |
rs766104263 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792470 | GGTATCTTCTACTGT[A/G]GTAGGAAGACTAGGG | 7409 |
rs766111380 | snp | A/G | 1.67086e-05 | 0.00289033 | intron-variant | VAV1 | GRCh38.p7 | 19:6825126 | TCAACATTGAGGTGA[A/G]CCGGCCGATCCCCAG | 7409 |
rs766114767 | snp | C/T | 1.78391e-05 | 0.00298651 | intron-variant | VAV1 | GRCh38.p7 | 19:6847958 | ATGGGGACCCAGGCA[C/T]GGGGACCGTGCCACC | 7409 |
rs766117416 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829530 | GACAGGTGGTAGACC[C/G]ATCCAGAGAAGGCGG | 7409 |
rs766167606 | snp | A/G/T | 3.30258e-05 | 0.0040635 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833256 | CTTTGAGGAGACCAC[A/G/T]TCCTGCAAGGCCTGT | 7409 |
rs766176894 | snp | A/G | 3.30437e-05 | 0.00406457 | intron-variant | VAV1 | GRCh38.p7 | 19:6773027 | GTGAGCCCTCCGCGG[A/G]CAGGTGTGCTGAGGG | 7409 |
rs766208722 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786058 | TGTTTTATTTTTCTC[C/T]ATAGCACTTAGTGCT | 7409 |
rs766216385 | snp | A/G | 6.60698e-05 | 0.00574722 | intron-variant | VAV1 | GRCh38.p7 | 19:6773023 | CCAGGTGAGCCCTCC[A/G]CGGGCAGGTGTGCTG | 7409 |
rs766288712 | in-del | -/AC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829395 | AGGTGGGTGGAGCCA[-/AC]ACAGATCTGGGGTGG | 7409 |
rs766290863 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802424 | AGGAAGTCCTTTCTG[G/T]TGGTCTAACTGCAGT | 7409 |
rs766331513 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796447 | CCTTCCTCCCTCCCC[C/G]TCGCTTACTCTGCTC | 7409 |
rs766357198 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816089 | CAGTGGCGCAATCTC[A/G]GCTCACTGCAAGCTC | 7409 |
rs766403969 | snp | A/G | 1.78857e-05 | 0.00299041 | intron-variant | VAV1 | GRCh38.p7 | 19:6833481 | AGAATATTTGGCCCT[A/G]TCTGTAAAGGTCACT | 7409 |
rs766422057 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854213 | ATGGAGATCTCTCAC[A/G]GTGGGAGGGAAGGAA | 7409 |
rs766450193 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | VAV1 | GRCh38.p7 | 19:6836934 | AGATGGCAGGTGGGG[C/T]TATGGATCCTATAAC | 7409 |
rs766552243 | snp | C/T | 2.06039e-05 | 0.0032096 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772780 | GAGGCTGCGAGGGTG[C/T]ACGGCCGGCCCTGGG | 7409 |
rs766654616 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844672 | TAGAACACGTAAGAG[A/G]CAGGGTCAGGATTTG | 7409 |
rs766662788 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856989 | GAGGGAGCCTGCCTG[A/G]TGTGTGGAGGGGCAG | 7409 |
rs766681664 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803462 | CCAGCCCTGTTTTAG[C/T]TAGTCCTCAATTTGG | 7409 |
rs766684151 | in-del | -/AAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843409 | GATGACGATGATGAC[-/AAT]GATGATGATGATAAT | 7409 |
rs766694551 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808164 | TAAAAATACAAAAAT[C/T]AGCCAGGTGTGGTGG | 7409 |
rs766743248 | snp | C/T | 1.76322e-05 | 0.00296914 | intron-variant | VAV1 | GRCh38.p7 | 19:6833160 | GACCTTCTTTTTTTT[C/T]TTTTTTTAATTTTCC | 7409 |
rs766747891 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807161 | AGGGGGGATGGTTTC[A/T]GGATGATTCAAATGC | 7409 |
rs766784124 | in-del | -/TATTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785849 | TTTTTAGTAGAGATG[-/TATTTT]GGGTTTCACCATGTT | 7409 |
rs766794586 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783731 | CCTCGGCCTCCCAAA[C/G]TGCTGGGATTACAGG | 7409 |
rs766837022 | in-del | -/AT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823466 | TCATTATTTAAAGAT[-/AT]ATATATATAAAGTAT | 7409 |
rs766858946 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800928 | CACCGCACCCAGCCG[C/T]TCACCATCTCTTTGT | 7409 |
rs766871525 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816646 | GCAGCATCCCCACAC[C/T]GATCTAAGCCTGCTT | 7409 |
rs766888673 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779539 | GACTTACATTTTGCT[C/T]GCCCTGTGCTAGACA | 7409 |
rs766892501 | snp | C/T | 1.65059e-05 | 0.00287275 | missense | VAV1 | GRCh38.p7 | 19:6850746 | GAGAAAAAGGCTTTC[C/T]GGGGGCTTACGGTAA | 7409 |
rs766913911 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799463 | GTGAGCCACCATGCC[C/T]GGCCTATACTTTAAG | 7409 |
rs766939845 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791554 | ATCTCAAGGTCCCTG[A/G]GACATCGCCCCATCT | 7409 |
rs766949121 | snp | C/T | 0.000115574 | 0.00760088 | intron-variant | VAV1 | GRCh38.p7 | 19:6828055 | CTGCCTCAGTTTCCC[C/T]ATTGTTCTCTGATTC | 7409 |
rs766949914 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811889 | TCTAGTTCCAGGTCG[C/G]GGGGCTTTTCCCCGC | 7409 |
rs766968161 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838722 | TCCATCTATTCTATC[C/T]ATCTATCTCTTAATT | 7409 |
rs766989630 | snp | C/T | 1.64966e-05 | 0.00287194 | intron-variant | VAV1 | GRCh38.p7 | 19:6829951 | GAACTATGGGGTCCT[C/T]CACGCAGTCGGCAGC | 7409 |
rs767017444 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840936 | GCATGCACCACCACA[C/T]CAAGCTAATTTTTGT | 7409 |
rs767040794 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829138 | CACAGATCTGGGAGG[A/C]GCCTGGGCAGGGATG | 7409 |
rs767091715 | snp | C/T | 1.65499e-05 | 0.00287657 | intron-variant | VAV1 | GRCh38.p7 | 19:6832088 | AGCTCTGCTTCCCTG[C/T]AGTGGAGCCACATGT | 7409 |
rs767140238 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855273 | TTGCATCGATGAGGA[A/G]TTTTGTTAAAACATT | 7409 |
rs767163670 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817725 | GGGGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs767189353 | snp | A/G | 4.94189e-05 | 0.00497062 | missense | VAV1 | GRCh38.p7 | 19:6820766 | AGTTCGGCCTCAAGC[A/G]GAGCGAGCTCTTCGA | 7409 |
rs767216446 | in-del | -/TTT/TTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787020 | TTGACACGCTGTCTA[-/TTT/TTTT]TTTTTTTTTTTTTTT | 7409 |
rs767262513 | snp | C/T | 1.65113e-05 | 0.00287322 | intron-variant | VAV1 | GRCh38.p7 | 19:6820653 | TGGGGGTCAGTTTCT[C/T]CCCTGCCCTTTCGTA | 7409 |
rs767287565 | snp | A/G | 1.64963e-05 | 0.00287192 | intron-variant | VAV1 | GRCh38.p7 | 19:6828525 | TGACTCACCTGCTGC[A/G]GACACCCTCCTGGTA | 7409 |
rs767314837 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813045 | TGTTACCTATTTATT[A/G]CTAAGTAACAAATTA | 7409 |
rs767316990 | snp | A/G | 1.65754e-05 | 0.00287879 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848067 | GGACGGGACTTTCTT[A/G]GTGCGGCAGAGGGTG | 7409 |
rs767321559 | snp | A/G | | | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6853958 | ACAGTGGGAAGCACA[A/G]AGTATTTTGGCACAG | 7409 |
rs767363682 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785049 | CACCGCAGCCAAATC[A/G]GCCACCCAGCACAAT | 7409 |
rs767370819 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6822126 | GAGGTCCCACCCTTG[A/G]AGTCTTGGGGGGACA | 7409 |
rs767409927 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6833044 | AGTGTGGCCAAAGGG[C/T]GAAAACGACCCAAAA | 7409 |
rs767418500 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781673 | AGTGTAGTGGCGCAA[G/T]CTCAGCTCACTGCAA | 7409 |
rs767418706 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784148 | AGTCTCAGCTACTCA[A/G]GAAGTTGAGGCAGGA | 7409 |
rs767446096 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812098 | CTGCATCCACATGCA[A/G]GGAGAGATGGGAAAT | 7409 |
rs767489117 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823744 | ATCCCAGGCTCAGTC[C/T]TTTTCTGTATCCTCA | 7409 |
rs767493105 | snp | A/G | 1.66402e-05 | 0.00288441 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833591 | ACACAAGGAGTGTCT[A/G]GGGAGGGTCCCTCCA | 7409 |
rs767551758 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844367 | ATTACAGGCACCTGC[C/T]GCCACACCTGGCTAA | 7409 |
rs767579709 | snp | C/T | 1.74598e-05 | 0.00295459 | intron-variant | VAV1 | GRCh38.p7 | 19:6833164 | TTCTTTTTTTTTTTT[C/T]TTTAATTTTCCCCTG | 7409 |
rs767593961 | snp | C/G | 1.65002e-05 | 0.00287225 | splice-donor-variant | VAV1 | GRCh38.p7 | 19:6773012 | CCCCAGATGTCCCAG[C/G]TGAGCCCTCCGCGGG | 7409 |
rs767609986 | snp | G/T | 1.65026e-05 | 0.00287246 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772888 | CGTGACCTGGGATGG[G/T]GCTCAGGTGTGTGAA | 7409 |
rs767616858 | snp | C/T | 1.64754e-05 | 0.00287009 | intron-variant | VAV1 | GRCh38.p7 | 19:6843091 | CCCTCTGCTGTCAAG[C/T]TGGGGTCTTTACACT | 7409 |
rs767644709 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807108 | TTTGGTAGCAGTGAC[A/C]GGTTTTGTGGAAGAC | 7409 |
rs767665041 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797774 | AAAAGAGTAGGAGCA[A/C]AAATATGACTAAGAC | 7409 |
rs767676435 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843400 | TACAATGATGATGAC[G/T]ATGATGACAATGATG | 7409 |
rs767696579 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835103 | TTTCTTCTTATTATT[A/G]CTTACTATGTAATTA | 7409 |
rs767703706 | in-del | -/ATCCATCCATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776078 | TCCATCCATCCATTT[-/ATCCATCCATCC]ATCCATCCATCCATC | 7409 |
rs767719589 | in-del | -/T | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857470 | AAGCCCCCTTACCAA[-/T]CCACAGACAAAGCCC | 7409 |
rs767776261 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799324 | AGGTGTGCGCCACCA[C/T]GCCTGGCTAATTTTT | 7409 |
rs767854229 | snp | C/G/T | 3.29909e-05 | 0.00406135 | missense, intron-variant | VAV1 | GRCh38.p7 | 19:6853049 | TTCCCCTTCAAGGAG[C/G/T]CTGAAAAGAGAACCA | 7409 |
rs767902451 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6825989 | CGGAGGTTGCAGTGA[G/T]TCAAGATCATGCCAC | 7409 |
rs767905021 | snp | C/T | 1.70006e-05 | 0.00291548 | intron-variant | VAV1 | GRCh38.p7 | 19:6828213 | CTCCACGTACCTACT[C/T]TCCTGTGTCTATAAA | 7409 |
rs767926458 | in-del | -/TTTTTTTTTTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850226 | TTGTTTGTTTCTTTG[-/TTTTTTTTTTTT]TTTTTTTTGTGATCT | 7409 |
rs767927458 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787577 | CAACTACTCCAGATT[G/T]ATTTATTTATTTATT | 7409 |
rs767949726 | in-del | -/A | 0.5 | 0 | intron-variant | VAV1 | GRCh38.p7 | 19:6833168 | TTTTTTTTTTTTTTT[-/A]ATTTTCCCCTGCCAG | 7409 |
rs767955641 | snp | C/G | 1.71457e-05 | 0.0029279 | intron-variant | VAV1 | GRCh38.p7 | 19:6852924 | GCCCCCTTATGGGCT[C/G]GCCCGCTGGGATAGC | 7409 |
rs767975682 | snp | C/G | 1.67256e-05 | 0.0028918 | intron-variant | VAV1 | GRCh38.p7 | 19:6821763 | CCCAGCCCCCAGGCC[C/G]CTGGCTCACACCCTC | 7409 |
rs768006508 | in-del | -/CA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777343 | ACAGTGGGAATAGCA[-/CA]CACACACACAAAAAC | 7409 |
rs768010898 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | VAV1 | GRCh38.p7 | 19:6833775 | TGTACCACAAATAAT[A/G]GGCAACAGCGCGGGG | 7409 |
rs768075621 | snp | A/C | 1.6473e-05 | 0.00286988 | missense | VAV1 | GRCh38.p7 | 19:6829817 | GACAAAGCTCTACTC[A/C]TCTGTAAGCGCAGGG | 7409 |
rs768082124 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837486 | CTTGATGGACCCCTC[A/G]CTCTTCATGATGACT | 7409 |
rs768101725 | snp | A/G | 1.64827e-05 | 0.00287073 | missense | VAV1 | GRCh38.p7 | 19:6772965 | ACAACCTGCTACCCC[A/G]TGCCATCAACCTGCG | 7409 |
rs768132811 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775267 | GCCCCATCTGTTAGA[A/C]CTGGCAGGGAGTCAA | 7409 |
rs768137939 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850304 | AGGCCCCTTTTAGTC[C/T]ATTTCCACCATGTTG | 7409 |
rs768192811 | in-del | -/CCG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796446 | CCTTCCTCCCTCCCC[-/CCG]CTCGCTTACTCTGCT | 7409 |
rs768193215 | snp | C/G | 1.72204e-05 | 0.00293427 | intron-variant | VAV1 | GRCh38.p7 | 19:6832223 | CCCGTCTTCCTCCCT[C/G]TTTCTGTCCACAGAG | 7409 |
rs768206590 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805254 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7409 |
rs768209602 | snp | C/T | 0.000111801 | 0.00747581 | intron-variant | VAV1 | GRCh38.p7 | 19:6826761 | GCTCCTCCCCAGGCC[C/T]TGGGGGCAGCAGGGA | 7409 |
rs768245500 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813482 | TCTTAACTTATGTAT[A/G]AATACTAGGAGCTAT | 7409 |
rs768262174 | snp | C/T | 1.64751e-05 | 0.00287007 | intron-variant | VAV1 | GRCh38.p7 | 19:6837067 | TGAGTGCCTCAAGTC[C/T]GAATGGAATAAGGGC | 7409 |
rs768265624 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796303 | AAATCATTTATTTGT[C/G]CTTCTTTATAGGGAC | 7409 |
rs768268673 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785521 | ATTTTTAGTAGAGAC[A/G]GAGTTTCACCATGTT | 7409 |
rs768307810 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786306 | ATGGGCCCAAGCTGC[C/T]TCGTGTTTTAAAAAT | 7409 |
rs768336734 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817741 | GCCCAGGCTGGAGTG[A/C]AGTGGCACCGTCGTG | 7409 |
rs768346508 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834997 | GCAGTGAGCCATGAT[C/T]ACGCCACTGCACGCC | 7409 |
rs768408061 | snp | G/T | 1.66921e-05 | 0.00288891 | intron-variant | VAV1 | GRCh38.p7 | 19:6852951 | TAGCATCTGCCATGT[G/T]GTCCGCCTTCTAGGA | 7409 |
rs768435430 | snp | G/T | 1.65274e-05 | 0.00287462 | intron-variant | VAV1 | GRCh38.p7 | 19:6821704 | CCACCTGGGCCTTGG[G/T]CCATTTAGCCCCAGT | 7409 |
rs768443541 | in-del | -/TC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814715 | CTTTCTTTCTTTCTT[-/TC]TTTCTTTCTTTCTTT | 7409 |
rs768491466 | snp | C/G | 1.65916e-05 | 0.00288019 | intron-variant | VAV1 | GRCh38.p7 | 19:6828179 | TTCTCCAGGTGCCAG[C/G]CACATCTCTAGGCGT | 7409 |
rs768512807 | in-del | -/CCCCTCCCCTGCCCCCCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798905 | GTTTCCTCCATCCCA[-/CCCCTCCCCTGCCCCCCC]CCCCTCCCTGCCTCC | 7409 |
rs768574214 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832813 | GCAAAATTCCAACAA[C/T]AAAAATCTAACAATT | 7409 |
rs768614314 | snp | A/G | 1.66286e-05 | 0.0028834 | missense | VAV1 | GRCh38.p7 | 19:6825354 | ATGAAGGAAGCCCTG[A/G]GCACCCCTGGCGCAG | 7409 |
rs768617299 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778785 | TGGTGGCTCGTGCCT[A/G]TAATCCCAGCACTTT | 7409 |
rs768620399 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817257 | TTAGTAGAAATGGGG[C/T]TTCACCATGTTGCCC | 7409 |
rs768643429 | snp | C/T | 1.70284e-05 | 0.00291786 | missense | VAV1 | GRCh38.p7 | 19:6848021 | GCCCCATGGAGCGGG[C/T]AGGGGCAGAGAGCAT | 7409 |
rs768680198 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800402 | GCAACCTCTGCCTCC[G/T]GGGTTCAAGCGATTC | 7409 |
rs768735270 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811680 | CTGCATATAATTACT[C/G]TAAGAATCGGCAAGA | 7409 |
rs768738686 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807623 | AGGCTGAGGTGGGAG[A/G]ATCACTTGAGCCCAG | 7409 |
rs768772527 | snp | A/G | 1.70551e-05 | 0.00292015 | intron-variant | VAV1 | GRCh38.p7 | 19:6828938 | TGGGATGGAGCCTGG[A/G]CAAAGGGGTGGGACC | 7409 |
rs768785732 | in-del | -/TATT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804416 | GGTCCTATTTATATT[-/TATT]TATTTATTTATTTAT | 7409 |
rs768801763 | snp | C/G | 3.36106e-05 | 0.00409929 | intron-variant | VAV1 | GRCh38.p7 | 19:6833334 | ACTTGGTCATCAGTT[C/G]CTTGCTAGAGAAGAT | 7409 |
rs768853046 | snp | C/T | 4.96249e-05 | 0.00498096 | intron-variant | VAV1 | GRCh38.p7 | 19:6848141 | CTCCCTGACTCATAC[C/T]CTTTTGGGGCCTGGG | 7409 |
rs768881027 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839371 | TAAAACTGACCGTTA[C/T]AATGAAAAATTCAGA | 7409 |
rs768898075 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799268 | CGCCTCCCAGGTTCA[A/G]GCGATTCTTCTGCCT | 7409 |
rs768900256 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6841992 | ACACTTTGGGAGGCC[A/G]AGGCGGGTGGATCAC | 7409 |
rs768905072 | snp | A/C | 1.64743e-05 | 0.00287 | missense | VAV1 | GRCh38.p7 | 19:6820736 | TTAGAACCTTCCTGT[A/C]CACCTGCTGTGAGAA | 7409 |
rs768921974 | snp | C/T | 0.000156493 | 0.00884433 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833537 | TCTCAGAGGTACCTT[C/T]TATCAGGGCTACCGC | 7409 |
rs768929801 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838128 | ATCTATCTATCTATC[C/T]ATCTATCCATGCATC | 7409 |
rs769020832 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810969 | TTTCAACTGTTGTTC[C/T]AAAACCTTTGTCCTC | 7409 |
rs769028112 | snp | C/T | 1.64849e-05 | 0.00287092 | intron-variant | VAV1 | GRCh38.p7 | 19:6820854 | CCAAAGACTGAGTTT[C/T]AGTTAATTTCTATTG | 7409 |
rs769094682 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842824 | GGGCAGCATAGTGAG[A/C]CTCTGTCCCTAAAAA | 7409 |
rs769101973 | snp | A/G | 4.94776e-05 | 0.00497357 | intron-variant | VAV1 | GRCh38.p7 | 19:6828748 | CAGGGGTGTGGCCAC[A/G]TGGGGAGAGTGTGTG | 7409 |
rs769119085 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794384 | GTGGCCCATGCCTGT[A/G]ATTTCAGCATTCTGG | 7409 |
rs769122198 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790842 | TCTGAGTTGTCAGGT[C/G]TTTGCCATGGAAGGG | 7409 |
rs769155635 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807456 | CTGACAGGAGGTGGG[A/G]CTCAGGTGGTAATGC | 7409 |
rs769174850 | in-del | -/GCCCTTCCCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784998 | TCTGTCCATCTCTCA[-/GCCCTTCCCT]GCTCCCTCTCTACCC | 7409 |
rs769194270 | snp | C/T | 0.000285919 | 0.0119531 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772840 | ATGCACCCACTGGCT[C/T]ATCCAGTGCCGGGTG | 7409 |
rs769197914 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830513 | GGCACGGTCTTGGCT[C/G]ACTGCAACCTCTGGC | 7409 |
rs769200222 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800853 | CTGGTCTTGAACCCC[-/T]TGACCTCAAGTGATC | 7409 |
rs769258756 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783470 | CCATCACCTCCATCC[-/T]TTTTTTTTTTTTTTT | 7409 |
rs769309510 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794668 | TTCTAGGTACTTTAT[A/T]CTTATTAACACTTTT | 7409 |
rs769323119 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779998 | CGCCTGTAGTCCCAG[C/T]TACTCGGGAGGCTGA | 7409 |
rs769333944 | snp | C/T | 3.3465e-05 | 0.0040904 | missense | VAV1 | GRCh38.p7 | 19:6821834 | GGTGATGAAGACATC[C/T]ACAGTGGCCTGTCCG | 7409 |
rs769340930 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774921 | ACCATGCCTGCCTAA[-/TT]TTTTTTTTTTTTTTT | 7409 |
rs769350748 | snp | G/T | 1.65105e-05 | 0.00287315 | intron-variant | VAV1 | GRCh38.p7 | 19:6857021 | AGGAGGATGTGCAGA[G/T]GTTGCACTGATGAAC | 7409 |
rs769356900 | snp | A/G | 1.66765e-05 | 0.00288756 | intron-variant | VAV1 | GRCh38.p7 | 19:6836590 | GCTGGGGCCACAAGA[A/G]TGATGGGGTGGGACC | 7409 |
rs769383906 | snp | C/G | 0.000133136 | 0.00815783 | intron-variant | VAV1 | GRCh38.p7 | 19:6850782 | AATGTCCGCTCAATC[C/G]CAGCTTTCCAGAACC | 7409 |
rs769393182 | in-del | -/CCTGGGTTCAAAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778492 | CTTTGGAGAGCCACA[-/CCTGGGTTCAAAT]CCTGGGTTCAAATTC | 7409 |
rs769393831 | snp | C/T | 1.66004e-05 | 0.00288096 | missense | VAV1 | GRCh38.p7 | 19:6833198 | GCTCCAACATCTATC[C/T]GGAGAATGCCACCGC | 7409 |
rs769397830 | snp | A/G | 1.65192e-05 | 0.00287391 | intron-variant | VAV1 | GRCh38.p7 | 19:6828042 | CTGTTTCTGGGACCT[A/G]CCTCAGTTTCCCCAT | 7409 |
rs769407801 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777174 | ATCCACCCGTCTACT[C/T]ATCTATCCATTCATC | 7409 |
rs769413379 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795547 | CTGGTTCTCAATTGA[C/T]GGGAGCTGTCAATAT | 7409 |
rs769440187 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806669 | AAGATCCGGGATTTG[A/C]ACTCTCTCATTGGTC | 7409 |
rs769451080 | snp | A/G | 0.000148267 | 0.00860879 | intron-variant | VAV1 | GRCh38.p7 | 19:6833707 | TTCCTTTACCCTCCC[A/G]TAGATTTCCCAGGAA | 7409 |
rs769490230 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851486 | TGCATTCAGCCCTCA[A/G]ATATGTTATAGATAG | 7409 |
rs769502197 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832691 | CCTCTTCTTTCTCTT[C/T]CTCCTCCCTTTCCTC | 7409 |
rs769518456 | snp | C/T | 1.68055e-05 | 0.0028987 | intron-variant | VAV1 | GRCh38.p7 | 19:6828200 | CTCTAGGCGTGGGCT[C/T]CACGTACCTACTCTC | 7409 |
rs769615605 | snp | C/G | 3.364e-05 | 0.00410108 | intron-variant | VAV1 | GRCh38.p7 | 19:6821907 | CTGGAGCACCGTCCT[C/G]GGGGTGGAGGGTGTG | 7409 |
rs769633490 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799165 | ATGGAGGTTTTTTTG[G/T]TTGTTTCGCTTTGTT | 7409 |
rs769639780 | in-del | -/ACATAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835211 | TGTGTATATATATAT[-/ACATAC]ACACACACACACACA | 7409 |
rs769699052 | in-del | -/GT | 1.64879e-05 | 0.00287118 | frameshift-variant | VAV1 | GRCh38.p7 | 19:6857062 | TTTCCAGGTTGGCTG[-/GT]TCCCTGCCAACTACG | 7409 |
rs769767559 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789696 | TCCGCATCATGGGTT[C/T]GAGTGATTCTCCTGC | 7409 |
rs769820693 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799952 | CATTTCTCTTGAGTA[A/T]ATGCCTGGTAATGGA | 7409 |
rs769833488 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834347 | CTCCCAAGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 7409 |
rs769866550 | snp | A/G | 1.68707e-05 | 0.00290432 | intron-variant | VAV1 | GRCh38.p7 | 19:6825260 | TTCCTGGCCCCCTGA[A/G]CCCTGGGCTCTGGTC | 7409 |
rs769890952 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819277 | CTATTGAGCCTTTAT[A/G]GGAACATATGAATAT | 7409 |
rs769945533 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851135 | GGGTACATGTATATA[C/T]GTGTATCTGTTTATT | 7409 |
rs769969950 | snp | C/G/T | 3.30171e-05 | 0.00406296 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6850676 | TGGTTCCAGATATAA[C/G/T]GTCGAGGTCAAGCAC | 7409 |
rs770040473 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831269 | AACTCTTCCGTTCGC[C/T]TCAGTTTTTGCCCTG | 7409 |
rs770047726 | snp | A/C | 1.67452e-05 | 0.0028935 | intron-variant | VAV1 | GRCh38.p7 | 19:6828915 | GGTGGGTGGAGTCAA[A/C]ATGGATCTGGGATGG | 7409 |
rs770080114 | snp | C/T | 1.64961e-05 | 0.00287189 | intron-variant | VAV1 | GRCh38.p7 | 19:6857040 | GCACTGATGAACTCC[C/T]CGTCTGTTTCCAGGT | 7409 |
rs770085781 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781338 | ATATGAATTATTTCA[A/G]TTATACCACCACATG | 7409 |
rs770092750 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818674 | ATGAGGTCATCTGTG[G/T]GGGCCCTAATGCACT | 7409 |
rs770129307 | snp | A/G | 1.6486e-05 | 0.00287102 | intron-variant | VAV1 | GRCh38.p7 | 19:6837085 | ATGGAATAAGGGCAA[A/G]GGGTCCAGGGCGGGT | 7409 |
rs770136056 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793025 | CTTGGGCAAGTTATC[A/G]AATGCTTCAAGAAAG | 7409 |
rs770136826 | snp | C/T | 1.77495e-05 | 0.002979 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6822490 | GGAGGAGAAGTACAC[C/T]GACACGCTGGGCTCC | 7409 |
rs770182202 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802867 | GGAGATTTATTCATT[C/T]GACAGATTTTATTGA | 7409 |
rs770187705 | snp | A/G | 3.33433e-05 | 0.00408296 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772852 | GCTCATCCAGTGCCG[A/G]GTGCTGCCGCCCAGC | 7409 |
rs770237467 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773630 | GGGCCCAGTCCTGGG[A/C]TCAGAGAGTGGGTCC | 7409 |
rs770240874 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810452 | TTCATGCCTTTAATC[A/C]CAGCACTTTGAGAGG | 7409 |
rs770258364 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803879 | GCAGACAATGGAATA[C/T]TATTCAGCACTGAAG | 7409 |
rs770260218 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855972 | AACTGTTCTAGGCTC[C/T]TGGGATTCAGTGACA | 7409 |
rs770274666 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791149 | ATGGCCTGGGTGGGT[C/G]TTAAATATCTCCTCA | 7409 |
rs770285378 | in-del | -/AAAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845403 | AATAAACAAACAAAC[-/AAAT]AAATAAATAAATAAA | 7409 |
rs770312468 | snp | C/G | 8.2411e-05 | 0.00641862 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772978 | CCATGCCATCAACCT[C/G]CGTGAGGTCAACCTG | 7409 |
rs770370370 | in-del | -/TATA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838332 | ATCTATCTATCTATC[-/TATA]TGTCTATCTATCCAT | 7409 |
rs770387358 | snp | G/T | 1.64746e-05 | 0.00287002 | intron-variant | VAV1 | GRCh38.p7 | 19:6843181 | GGTGAGTAGAAACAT[G/T]TATTTTTGTTTCAAT | 7409 |
rs770437079 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808757 | TAAAGACAATATTTG[C/T]TATTCCAATTAATTT | 7409 |
rs770454168 | in-del | -/ATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776077 | TCCATCCATCCATTT[-/ATCC]ATCCATCCATCCATC | 7409 |
rs770460454 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855182 | CTCAGAAATATGTTT[A/G]TGTAATGAAGACAAG | 7409 |
rs770477714 | snp | C/T | 3.14896e-05 | 0.00396785 | intron-variant | VAV1 | GRCh38.p7 | 19:6833154 | AATACTGACCTTCTT[C/T]TTTTTTTTTTTTTAA | 7409 |
rs770481318 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806616 | CACTCTTGACCAACA[C/G]AGCGGAGAGTAAATC | 7409 |
rs770497549 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831505 | TTTTAGTAGAGACGG[A/G]GTTTCACCACATTGG | 7409 |
rs770499467 | snp | A/G | 1.65078e-05 | 0.00287291 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6852973 | CTTCTAGGAGCTGGT[A/G]GAGTTTTACCAGCAG | 7409 |
rs770520420 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794516 | TCTCAAAACAAAACA[A/G]AAAAACAAAGAGGAT | 7409 |
rs770576980 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788566 | ATTTTTAGTAGAGAC[A/G]GGGTTTCACCAGATT | 7409 |
rs770591924 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843649 | TGTTTCAGCATTCCT[A/C]TCTGGAAAATAGCTT | 7409 |
rs770603049 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775675 | CTTTGAAGCCCGGCC[A/G]TGTGTCTGGTATGTA | 7409 |
rs770625517 | snp | C/T | 4.99014e-05 | 0.00499482 | intron-variant | VAV1 | GRCh38.p7 | 19:6836421 | CTGTACTCCTGTACC[C/T]TGTCCTCCAGGTCTG | 7409 |
rs770637142 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780238 | TCTGTTTCCTGGTTT[C/G]TCATCTGTAAAATGA | 7409 |
rs770645311 | snp | C/G | | | missense | VAV1 | GRCh38.p7 | 19:6843139 | TGTATTCTTAGGGCC[C/G]TCCTCAGGACCTGTC | 7409 |
rs770661723 | snp | A/G | 7.58179e-05 | 0.00615656 | intron-variant | VAV1 | GRCh38.p7 | 19:6822195 | CTGGGAGAGGTCCAA[A/G]GGATCCCTGACCTCA | 7409 |
rs770680601 | snp | A/T | 1.66574e-05 | 0.0028859 | intron-variant | VAV1 | GRCh38.p7 | 19:6832067 | GGGGGCAGTGCCTTC[A/T]GTCTGAGCTCTGCTT | 7409 |
rs770699245 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798711 | AATCAGGGTCTCCCT[A/G]TGTTGCCCAGACTGG | 7409 |
rs770714689 | snp | C/T | 1.65798e-05 | 0.00287917 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822290 | GGAAGGCGACGAGAT[C/T]TATGAGGACCTCATG | 7409 |
rs770727468 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824793 | CCTCAGGCTCCCAAA[A/G]TGCTGGGATTGCAGG | 7409 |
rs770796277 | in-del | -/GGGAA | 1.83734e-05 | 0.0030309 | intron-variant | VAV1 | GRCh38.p7 | 19:6832249 | AGAGGGGCAGGGGCT[-/GGGAA]GGGAAGGAGGAACGT | 7409 |
rs770809171 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777112 | ATCCATCTACTCATC[-/CATC]CATCCATCCATCCAT | 7409 |
rs770820908 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856152 | ATACAAAAAAATTAG[C/T]TGGGCATTGTGGCGT | 7409 |
rs770828726 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786720 | CCTGGGAGATGGAGG[A/T]TGCAGTGAACCACGA | 7409 |
rs770850991 | snp | C/T | 1.67262e-05 | 0.00289185 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825365 | CCTGGGCACCCCTGG[C/T]GCAGCCAATCTCTAC | 7409 |
rs770852411 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836713 | GACTGAGACTTCTGG[G/T]CATGGCTTTTCTGAG | 7409 |
rs770882119 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797356 | TAAAGTAAGAATAGT[A/T]TGAATTACAAAGAAT | 7409 |
rs770883671 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837912 | ACTATTATTTAATTC[A/C]TAGTCTGTATTTAAA | 7409 |
rs770895701 | snp | A/C | 3.29582e-05 | 0.00405931 | intron-variant | VAV1 | GRCh38.p7 | 19:6828796 | GAGACCCTTGCTAGA[A/C]CCCCTGCCTACTGCA | 7409 |
rs770950776 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834405 | CATGTCACCACGCTC[A/G]GCTAATTTTTGTATT | 7409 |
rs770951101 | snp | A/G | 0.000158558 | 0.00890247 | intron-variant | VAV1 | GRCh38.p7 | 19:6847966 | CCAGGCACGGGGACC[A/G]TGCCACCTCTGTCCT | 7409 |
rs770953265 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849741 | CACCCAGTGCATCCA[C/T]GCTGCTGCAATGCAC | 7409 |
rs770975416 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781193 | TAATCGTGAATCATC[A/G]TGCTCCACCCAGTCC | 7409 |
rs771052840 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830292 | TCGATCTCTTGACCC[C/T]GTGATCCACCTGCCT | 7409 |
rs771056241 | snp | C/T | 1.65913e-05 | 0.00288017 | intron-variant | VAV1 | GRCh38.p7 | 19:6848157 | CTTTTGGGGCCTGGG[C/T]CCTGCGGGCCTGGGA | 7409 |
rs771085140 | snp | C/T | 9.89152e-05 | 0.00703192 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6857077 | GTTCCCTGCCAACTA[C/T]GTGGAGGAAGATTAT | 7409 |
rs771097008 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810030 | AAAAATAAAAATAAC[A/G]TTATCTGGGCATGGT | 7409 |
rs771111918 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791915 | AATGAAGGAGCTTCT[A/G]GAAGGAAGGGAGTGA | 7409 |
rs771115216 | snp | A/C | 1.64751e-05 | 0.00287007 | missense | VAV1 | GRCh38.p7 | 19:6833725 | GATTTCCCAGGAACT[A/C]TGAAGAAGGTAAGAC | 7409 |
rs771143892 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847327 | TCCTGCCTCCCGCAG[-/C]CCCCCGGGAACCAAG | 7409 |
rs771147677 | snp | G/T | 1.68235e-05 | 0.00290026 | intron-variant | VAV1 | GRCh38.p7 | 19:6828923 | GAGTCAACATGGATC[G/T]GGGATGGAGCCTGGG | 7409 |
rs771198282 | snp | G/T | 1.69057e-05 | 0.00290733 | intron-variant | VAV1 | GRCh38.p7 | 19:6825154 | CAGCCCTCTTGGGTC[G/T]GTCTAGTGCGGATAA | 7409 |
rs771202671 | snp | A/G | 0.000181268 | 0.00951847 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825064 | GCAGCATTTCTTGAA[A/G]CCCCTGCAACGGTTC | 7409 |
rs771240393 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791373 | GAGGTCCTTGAGATA[C/T]TTCCTCATCTTGAGG | 7409 |
rs771240640 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802688 | TGCCACTCTCTAAGA[A/G]GCACCAGGAGCAGCT | 7409 |
rs771269172 | snp | A/G | 3.29777e-05 | 0.00406051 | missense | VAV1 | GRCh38.p7 | 19:6772995 | GTGAGGTCAACCTGC[A/G]CCCCCAGATGTCCCA | 7409 |
rs771289785 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801953 | GGCACGATGCCAGCA[C/T]AGTGGGTGCCCGCCT | 7409 |
rs771333820 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813413 | TTCCACCCTGTTCTT[A/T]TAGTGACACATGGCC | 7409 |
rs771351847 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840502 | AGTAGAGTTTCACCG[C/T]GTTAGCCAGGATGGT | 7409 |
rs771359400 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795773 | ACTGCAACCTCCGCC[C/T]CCTGGGTTCAAGTGA | 7409 |
rs771365045 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854902 | GGAAAGCATTCCAGA[C/G]AGAAGGACCAGTGTG | 7409 |
rs771403086 | snp | C/T | 1.75696e-05 | 0.00296386 | intron-variant | VAV1 | GRCh38.p7 | 19:6847972 | ACGGGGACCGTGCCA[C/T]CTCTGTCCTTGGTGT | 7409 |
rs771420875 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776451 | CCATCCATCCACCCA[C/T]CCATCCACCCACCCA | 7409 |
rs771427926 | in-del | -/ATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838429 | TCCATCCATCCATCC[-/ATC]CATCCATCTATCATC | 7409 |
rs771483769 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774081 | TTCAGGGGCAGGGCC[A/G]TTGGTGGAAGAGATC | 7409 |
rs771488023 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853466 | CGGTGGCTCATGCCT[A/G]TAACTCCAGCACTTC | 7409 |
rs771508178 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775481 | CGGGAACCCAGATGG[A/G]GTCAGGCTTTATGCA | 7409 |
rs771513183 | snp | A/G | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857407 | GCTAGGAGAGAGATG[A/G]GGAGAGAGTGTGCCA | 7409 |
rs771559881 | snp | A/G | 1.65263e-05 | 0.00287452 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6836538 | CATTGTGGAGCTCAC[A/G]AAGGCTGAGGCTGAA | 7409 |
rs771597854 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785366 | TAACGGGGTCTCTGT[C/T]TATTGTCCAGGCTGG | 7409 |
rs771600077 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850136 | GTGAATTTCCCTTAC[-/T]TTTTTTTTTTTTTGA | 7409 |
rs771602703 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830278 | TGGCCAGGATGGTCT[C/G]GATCTCTTGACCCCG | 7409 |
rs771609375 | snp | A/G | 0.000103189 | 0.00718217 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822311 | GGACCTCATGCGCTC[A/G]GAGCCCGTGTCCATG | 7409 |
rs771624229 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848655 | TGATCCACCCGCCTC[A/G]GCCTCCCAAAGTGTT | 7409 |
rs771634296 | snp | C/T | 1.66048e-05 | 0.00288134 | intron-variant | VAV1 | GRCh38.p7 | 19:6836428 | CCTGTACCCTGTCCT[C/T]CAGGTCTGCCCAAGA | 7409 |
rs771666124 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823851 | GTTCAATGGTTTTTG[A/G]CACACACAAGATTAT | 7409 |
rs771680595 | snp | C/T | 5.09437e-05 | 0.00504671 | intron-variant | VAV1 | GRCh38.p7 | 19:6832210 | GGCCATGTGAGTCCC[C/T]GTCTTCCTCCCTCTT | 7409 |
rs771682522 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789260 | CTCTCTCCTTTCTTC[-/T]TTTTTTTTTTTTGAC | 7409 |
rs771721166 | in-del | -/AA | 1.64914e-05 | 0.00287149 | frameshift-variant | VAV1 | GRCh38.p7 | 19:6832156 | GCTGTTCTTCAAGAC[-/AA]GAGAATTGAAGAAGA | 7409 |
rs771728616 | snp | A/G | 1.648e-05 | 0.0028705 | missense | VAV1 | GRCh38.p7 | 19:6854061 | TCCTTAACAAGAAGG[A/G]ACAGCAAGGCTGGTG | 7409 |
rs771744357 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824700 | CCGTGCCCAGCTTAT[G/T]TTTGTAGTTTTAGTA | 7409 |
rs771780183 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810588 | CGGGCGCCTGTAATC[A/G]CAGCTACTCAGGAGG | 7409 |
rs771789009 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835157 | GCAAGAGTCAAAATT[A/G]GAAACAACCCGTGTC | 7409 |
rs771801566 | snp | A/G | 3.30186e-05 | 0.00406303 | missense | VAV1 | GRCh38.p7 | 19:6836507 | TTGGACCCTTTCTAC[A/G]GCTCAACCCTGGAGA | 7409 |
rs771827278 | snp | C/T | 9.24172e-05 | 0.00679706 | missense | VAV1 | GRCh38.p7 | 19:6826628 | TTCCTCGTCTATGGC[C/T]GCTACTGCAGCCAGG | 7409 |
rs771846103 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799419 | ATAATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 7409 |
rs771873669 | snp | A/C/G | 5.58928e-05 | 0.00528619 | utr-variant-5-prime | VAV1 | GRCh38.p7 | 19:6772801 | CGGCCCTGGGCAGGC[A/C/G]GTAGCCATGGAGCTG | 7409 |
rs771917300 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796404 | CGGTTTGGGCATATC[A/G]GCACCTGAGACCACC | 7409 |
rs771949630 | snp | C/T | 0.000217865 | 0.0104348 | intron-variant | VAV1 | GRCh38.p7 | 19:6826745 | CTCGGGGGCCTCTCC[C/T]GCTCCTCCCCAGGCC | 7409 |
rs771999820 | snp | A/G | 1.64933e-05 | 0.00287165 | intron-variant | VAV1 | GRCh38.p7 | 19:6821589 | CGTGGGGGTGTACAA[A/G]GGGCTCACTGAGTGG | 7409 |
rs772003183 | snp | C/T | 1.65094e-05 | 0.00287305 | missense | VAV1 | GRCh38.p7 | 19:6821677 | CCCAGAACAGGGGGA[C/T]CATGTGAGTAACCAC | 7409 |
rs772024253 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808829 | AATAACTTGGCTGGG[G/T]TAGGTAGTCTAGGAG | 7409 |
rs772056486 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817334 | CTTCCAAAGTGCTGC[A/G]ATTACAGGGATGAGT | 7409 |
rs772081545 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781037 | CCTCAGCCTCCTGAG[C/T]AGCTGGGACTACAGA | 7409 |
rs772113692 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791174 | TCCTCATCTTGAAGT[C/T]CTTGAGATACCTCCT | 7409 |
rs772117266 | in-del | -/CT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832665 | TTCTTCCTCCTCCTC[-/CT]CCTCTTCCTCCTCTT | 7409 |
rs772144121 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6816778 | ACCAGCCTGGACAAC[A/G]TGGTGAAATCCCCAT | 7409 |
rs772204705 | snp | C/T | 1.64846e-05 | 0.0028709 | intron-variant | VAV1 | GRCh38.p7 | 19:6833656 | AGGCTGGGAGGTGAG[C/T]TTGGTTCTCTTTGGA | 7409 |
rs772249693 | snp | A/G | 3.29679e-05 | 0.00405991 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825076 | GAAGCCCCTGCAACG[A/G]TTCCTGAAACCTCAA | 7409 |
rs772292946 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827943 | AGATATGATGCTTTG[G/T]CCTCTAGAAAAATTC | 7409 |
rs772340180 | in-del | -/TCTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838716 | CCATCATCCATCTAT[-/TCTA]TCTATCTATCTCTTA | 7409 |
rs772372299 | snp | C/T | 3.39951e-05 | 0.00412267 | intron-variant | VAV1 | GRCh38.p7 | 19:6825163 | TGGGTCTGTCTAGTG[C/T]GGATAACCTGCTGCC | 7409 |
rs772372999 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6812638 | CCTGGATGACAGAGG[C/G]AGACTCTATCTCAAA | 7409 |
rs772377506 | in-del | -/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823131 | TTTATCTATCTATCT[-/TT]TTTTTTTTTTTGAGA | 7409 |
rs772377777 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808406 | GTCATCCTTGGCAAA[C/T]TAGGAGGTAAGTCAC | 7409 |
rs772403542 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851440 | TTCTGTCTTGGCCTC[C/T]CAAAGTGTTGGGATT | 7409 |
rs772422503 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826873 | CAGCCAAGCAGAGGA[A/G]ATGGAGAAGAACAGA | 7409 |
rs772426650 | snp | A/C | 4.96685e-05 | 0.00498315 | missense | VAV1 | GRCh38.p7 | 19:6825324 | CTTCGTGTTCATACT[A/C]ACTTCCTAAAGGAGA | 7409 |
rs772429898 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811826 | TTTCAGTGACTTCAC[A/G]TGGTAAAAATTGATT | 7409 |
rs772472419 | snp | C/G | 0.000115962 | 0.00761365 | intron-variant | VAV1 | GRCh38.p7 | 19:6822215 | CCCTGACCTCACAAC[C/G]CACAGCGACACGGTG | 7409 |
rs772475295 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839480 | ACCATGTTGGTCAGG[C/G]TGATCTCAAACTCCT | 7409 |
rs772497302 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832479 | CTTCTGGTTTCCTTC[C/T]TCCTCCTCCTCCTCT | 7409 |
rs772519762 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824391 | CATTTCATATAAAGG[A/G]CATCACATACTATGT | 7409 |
rs772533197 | snp | A/G | 3.52057e-05 | 0.00419543 | intron-variant | VAV1 | GRCh38.p7 | 19:6833521 | TTATGTGTTCCCTGC[A/G]TCTCAGAGGTACCTT | 7409 |
rs772609122 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819656 | GGATTTTAACCAACT[C/G]TACTGACGAGTCTGC | 7409 |
rs772626356 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784345 | GGGAGGAATTCAGCT[A/G]GGGATGAGGGAGCTG | 7409 |
rs772631746 | in-del | -/T/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827761 | TGCCACCACGCCAGC[-/T/TT]TATTTTTTTTTTTTT | 7409 |
rs772674111 | snp | A/T | 1.69447e-05 | 0.00291068 | intron-variant | VAV1 | GRCh38.p7 | 19:6853904 | AGAGAGTGAGTGGGT[A/T]TCTGCCCCAGACCCT | 7409 |
rs772698955 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830620 | AAATTTTGTATTTTT[A/G]GTAGAGACGAGGTTT | 7409 |
rs772762487 | snp | A/G | 1.67323e-05 | 0.00289239 | intron-variant | VAV1 | GRCh38.p7 | 19:6850795 | TCCCAGCTTTCCAGA[A/G]CCTAGGAGGACCCTC | 7409 |
rs772762824 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6856120 | GCCAACATGGCGAAA[C/G]CCTGTCTTAACTAAA | 7409 |
rs772766114 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6842872 | GATTTTTGCCAACCA[C/T]CTAAAAATGTAAAAA | 7409 |
rs772817579 | snp | C/T | 1.64746e-05 | 0.00287002 | intron-variant | VAV1 | GRCh38.p7 | 19:6833756 | TTTCCCGTGGTCCTT[C/T]CTGTGTACCACAAAT | 7409 |
rs772823641 | snp | A/T | 1.65776e-05 | 0.00287898 | intron-variant | VAV1 | GRCh38.p7 | 19:6852960 | CCATGTGGTCCGCCT[A/T]CTAGGAGCTGGTGGA | 7409 |
rs772860004 | snp | A/T | 1.67379e-05 | 0.00289287 | missense | VAV1 | GRCh38.p7 | 19:6821853 | GTGGCCTGTCCGACC[A/T]GATCGAGTGAGTGCT | 7409 |
rs772875776 | snp | C/T | 1.68474e-05 | 0.00290231 | intron-variant | VAV1 | GRCh38.p7 | 19:6828203 | TAGGCGTGGGCTCCA[C/T]GTACCTACTCTCCTG | 7409 |
rs772875948 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792433 | TGTCTAGGTTTACAG[C/T]TTAGGGACTTGCGTG | 7409 |
rs772904162 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786641 | TATAAAAATTACCTG[C/G]GTGTGATGGTGTGCG | 7409 |
rs772916197 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778570 | ATCTGTGAAACATAG[A/G]TAAAAATGGCACCTT | 7409 |
rs772928704 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776605 | ATCCACTCATCCATC[-/CATC]CATCCATCCATCCAC | 7409 |
rs772952667 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796418 | CGGCACCTGAGACCA[A/C]CCTTGGTTCACTCCC | 7409 |
rs772991992 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855295 | TAAAACATTGGAGGG[C/T]CAGTTTAATGAGCAG | 7409 |
rs773007761 | snp | C/T | 0.000236295 | 0.010867 | intron-variant | VAV1 | GRCh38.p7 | 19:6825261 | TCCTGGCCCCCTGAG[C/T]CCTGGGCTCTGGTCC | 7409 |
rs773020037 | in-del | -/AG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778708 | TCCAGCCTGGGCAAC[-/AG]AGAGAGACTTTGTCT | 7409 |
rs773079215 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808857 | GAGGGCCTCATTCAC[A/T]TATCTGCTGGTTGGC | 7409 |
rs773105393 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795867 | TTTTGTTATTTTTAG[A/T]AGAGACAGGGTTTCA | 7409 |
rs773147735 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847760 | GGGCTGAGCCATCCC[C/T]CCGAATCCATGTGTC | 7409 |
rs773169274 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | VAV1 | GRCh38.p7 | 19:6833644 | CGAGTGGGAGGGAGG[C/T]TGGGAGGTGAGCTTG | 7409 |
rs773187950 | snp | A/G | 1.67354e-05 | 0.00289265 | intron-variant | VAV1 | GRCh38.p7 | 19:6832055 | CCCACCCTCTGCGGG[A/G]GCAGTGCCTTCAGTC | 7409 |
rs773233437 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785224 | TTGCCCAGGCTGGAG[A/T]GCAGTGGTGTTATCA | 7409 |
rs773238903 | snp | C/T | 1.66394e-05 | 0.00288434 | missense | VAV1 | GRCh38.p7 | 19:6825358 | AGGAAGCCCTGGGCA[C/T]CCCTGGCGCAGCCAA | 7409 |
rs773244906 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777840 | CAGAGCCTTGCTGTC[C/T]CCCAGGATGGAGTGC | 7409 |
rs773288199 | snp | G/T | 1.65773e-05 | 0.00287895 | intron-variant | VAV1 | GRCh38.p7 | 19:6854108 | GGCCGGGTGAGGCAG[G/T]CAGGGCTGGGTGACG | 7409 |
rs773293298 | snp | A/G | 1.68892e-05 | 0.00290591 | missense | VAV1 | GRCh38.p7 | 19:6833560 | GCTACCGCTGCCATC[A/G]GTGCCGGGCATCTGC | 7409 |
rs773309888 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807788 | ATGAGGTCAGGAGTT[C/T]GAGACTAGTCTGACC | 7409 |
rs773332827 | snp | C/T | 0.00398405 | 0.0444539 | intron-variant | VAV1 | GRCh38.p7 | 19:6784204 | TGCTGCAGTGAGCTA[C/T]GATTGTGCTACCACT | 7409 |
rs773341851 | snp | C/G | 1.64972e-05 | 0.00287199 | intron-variant | VAV1 | GRCh38.p7 | 19:6828613 | GGTTCACCCCTGCCC[C/G]CTCCCCAGGACCTGG | 7409 |
rs773393977 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817850 | CGCCACCTTGCCTGG[A/C]TAATTTTTTGTGTTT | 7409 |
rs773404759 | snp | A/G | 1.68547e-05 | 0.00290294 | intron-variant | VAV1 | GRCh38.p7 | 19:6836614 | TGGGACCCAAGTGTA[A/G]GGTTATGGATTCATG | 7409 |
rs773405937 | snp | G/T | 1.71587e-05 | 0.002929 | intron-variant | VAV1 | GRCh38.p7 | 19:6822345 | GTGCGTGACGTGGAG[G/T]GTCGGGCCTGGGGAG | 7409 |
rs773419470 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791290 | TTGAGGTCCTTGAGA[C/T]ACCTCCTCATCTTAA | 7409 |
rs773492747 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819401 | AACCCTACTGACACC[-/T]TGATCTTGGACTTCT | 7409 |
rs773518767 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827986 | GGTGGAGAGCTGCTC[A/G]CGTATTTATTCAAAT | 7409 |
rs773601812 | snp | C/T | 1.66341e-05 | 0.00288388 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772856 | ATCCAGTGCCGGGTG[C/T]TGCCGCCCAGCCACC | 7409 |
rs773628836 | in-del | -/TATA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838335 | ATCTATCTATCTATA[-/TATA]TGTCTATCTATCCAT | 7409 |
rs773636185 | snp | A/G | 1.65012e-05 | 0.00287234 | intron-variant | VAV1 | GRCh38.p7 | 19:6837087 | GGAATAAGGGCAAGG[A/G]GTCCAGGGCGGGTCC | 7409 |
rs773638542 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | VAV1 | GRCh38.p7 | 19:6772979 | CATGCCATCAACCTG[C/T]GTGAGGTCAACCTGC | 7409 |
rs773650960 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811858 | CTTGTACACAAAACA[C/G]TACAATGCATGTGCT | 7409 |
rs773665675 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6845403 | AAATAAACAAACAAA[C/T]AAATAAATAAATAAA | 7409 |
rs773696752 | snp | C/T | 1.64822e-05 | 0.00287068 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6853036 | CACCACCTTGCAGTT[C/T]CCCTTCAAGGAGCCT | 7409 |
rs773740075 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772596 | GATTCTGCATGGAAG[A/G]CGTGGGGTGGGGCTG | 7409 |
rs773778887 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855248 | TATACACAAAAAATG[A/G]TGTGGATAATTGCAT | 7409 |
rs773847574 | snp | C/T | 1.78469e-05 | 0.00298716 | intron-variant | VAV1 | GRCh38.p7 | 19:6833156 | TACTGACCTTCTTTT[C/T]TTTTTTTTTTTAATT | 7409 |
rs773852044 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784372 | GCTGGGTGATAGCAA[C/G]TTCAGCAAAATGGGT | 7409 |
rs773863368 | snp | A/G | 3.29473e-05 | 0.00405864 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833949 | CAAAAAGAGGAATGA[A/G]CTGGGTGAGTTGGCA | 7409 |
rs773865248 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773680 | AGAGCTGCATTTTCT[C/T]GGCAGGGATTTCTGC | 7409 |
rs773904821 | snp | C/T | 1.65121e-05 | 0.00287329 | intron-variant | VAV1 | GRCh38.p7 | 19:6828049 | TGGGACCTGCCTCAG[C/T]TTCCCCATTGTTCTC | 7409 |
rs773988228 | snp | C/T | 1.66203e-05 | 0.00288268 | intron-variant | VAV1 | GRCh38.p7 | 19:6836422 | TGTACTCCTGTACCC[C/T]GTCCTCCAGGTCTGC | 7409 |
rs774038014 | snp | G/T | 1.66382e-05 | 0.00288424 | intron-variant | VAV1 | GRCh38.p7 | 19:6832071 | GCAGTGCCTTCAGTC[G/T]GAGCTCTGCTTCCCT | 7409 |
rs774041774 | snp | C/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6770917 | AGCACTTTGGAAGAC[C/T]AAGGCGGGCAGATCA | 7409 |
rs774080546 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853854 | ACTGAGGAGCCCTTT[A/T]TCCTGGAGTTACTGT | 7409 |
rs774093642 | snp | A/C/T | 3.29464e-05 | 0.00405861 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6820765 | AAGTTCGGCCTCAAG[A/C/T]GGAGCGAGCTCTTCG | 7409 |
rs774102567 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823638 | TGTCTCTCTGTCTCT[C/T]TCTTTATCTCTCACT | 7409 |
rs774143582 | in-del | -/TGCTCATCCATT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776125 | ATCCATCCATCCATC[-/TGCTCATCCATT]CATCCATCTGCTCAT | 7409 |
rs774177274 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6844126 | GAGGCTGAGAGAGGG[C/T]AAGTGAATTACTTAA | 7409 |
rs774187495 | in-del | -/ACACACACACACACACACACACAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836834 | TGAGCAGAGAGATGG[-/ACACACACACACACACACACACAC]ACACACACACACACA | 7409 |
rs774229997 | in-del | -/TTT/TTTCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785661 | TTCTTTCTTTCTTTC[-/TTT/TTTCT]TTTTTTTTTTTTTTT | 7409 |
rs774261638 | snp | C/T | 9.32271e-05 | 0.00682677 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826624 | TAGGTTCCTCGTCTA[C/T]GGCCGCTACTGCAGC | 7409 |
rs774270335 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855226 | GTTTACATTCTACTG[C/G]GGAAAATATACACAA | 7409 |
rs774337035 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806782 | GAGCCCCTCTCAGCC[A/C]ATGTTGCTAGAAGAG | 7409 |
rs774397672 | snp | A/C | 1.66098e-05 | 0.00288177 | intron-variant | VAV1 | GRCh38.p7 | 19:6848158 | TTTTGGGGCCTGGGC[A/C]CTGCGGGCCTGGGAA | 7409 |
rs774426463 | snp | C/T | 3.29685e-05 | 0.00405995 | missense | VAV1 | GRCh38.p7 | 19:6825074 | TTGAAGCCCCTGCAA[C/T]GGTTCCTGAAACCTC | 7409 |
rs774471900 | snp | A/G | 1.6486e-05 | 0.00287102 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6857078 | TTCCCTGCCAACTAC[A/G]TGGAGGAAGATTATT | 7409 |
rs774482557 | snp | C/T | 1.6492e-05 | 0.00287154 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772999 | GGTCAACCTGCGCCC[C/T]CAGATGTCCCAGGTG | 7409 |
rs774496919 | snp | A/G | 3.92349e-05 | 0.00442899 | intron-variant | VAV1 | GRCh38.p7 | 19:6822521 | ATCCAGCAGGTGGGC[A/G]CCTCCCACCCAGCGC | 7409 |
rs774526446 | snp | C/G | 1.64789e-05 | 0.0028704 | intron-variant | VAV1 | GRCh38.p7 | 19:6828798 | GACCCTTGCTAGACC[C/G]CCTGCCTACTGCATA | 7409 |
rs774529760 | snp | C/T | 1.75857e-05 | 0.00296522 | intron-variant | VAV1 | GRCh38.p7 | 19:6833161 | ACCTTCTTTTTTTTT[C/T]TTTTTTAATTTTCCC | 7409 |
rs774546176 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811061 | TTATTTTTGAGATGG[C/T]GTCTTGCTCTGTTGC | 7409 |
rs774566049 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800454 | AGCTGGGACTACAGG[C/T]GTGTTCCACCACACC | 7409 |
rs774581496 | snp | A/G | 1.68485e-05 | 0.00290241 | intron-variant | VAV1 | GRCh38.p7 | 19:6828925 | GTCAACATGGATCTG[A/G]GATGGAGCCTGGGCA | 7409 |
rs774589117 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783558 | CTGTTCAGTGCATCA[C/T]GGCAACCTCCGCCTC | 7409 |
rs774612756 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811689 | ATTACTGTAAGAATC[A/G]GCAAGAGAAGCTGGA | 7409 |
rs774697039 | in-del | -/ATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777247 | ACTATCCATCCATCC[-/ATCC]ATCCATCCATCCATC | 7409 |
rs774717994 | snp | A/G | 1.65866e-05 | 0.00287976 | intron-variant | VAV1 | GRCh38.p7 | 19:6833301 | GTGAGAATCTGGGAG[A/G]AGGGTCCTGCATACC | 7409 |
rs774793189 | snp | C/T | 1.65427e-05 | 0.00287595 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833214 | GGAGAATGCCACCGC[C/T]AACGGGCATGACTTC | 7409 |
rs774807565 | snp | G/T | 1.66037e-05 | 0.00288125 | intron-variant | VAV1 | GRCh38.p7 | 19:6773054 | AGGGTTGGAGACGGG[G/T]GTCCTCCCCGGGGCT | 7409 |
rs774816667 | snp | C/G | | | stop-gained, intron-variant | VAV1 | GRCh38.p7 | 19:6822487 | GACGGAGGAGAAGTA[C/G]ACTGACACGCTGGGC | 7409 |
rs774824315 | snp | A/G | 1.65825e-05 | 0.00287941 | missense | VAV1 | GRCh38.p7 | 19:6836432 | TACCCTGTCCTCCAG[A/G]TCTGCCCAAGATGGA | 7409 |
rs774829329 | in-del | -/AAAG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793336 | GAGACTCCATCTCAA[-/AAAG]AAAGAAAGAAAGAAA | 7409 |
rs774877233 | snp | A/G | 3.30486e-05 | 0.00406487 | missense | VAV1 | GRCh38.p7 | 19:6832094 | GCTTCCCTGCAGTGG[A/G]GCCACATGTTCCTCC | 7409 |
rs774885640 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784788 | CGTGAGCCACCATGC[C/G]CAGCCTCCATTCTAT | 7409 |
rs774921585 | snp | C/T | 1.68986e-05 | 0.00290672 | intron-variant | VAV1 | GRCh38.p7 | 19:6828207 | CGTGGGCTCCACGTA[C/T]CTACTCTCCTGTGTC | 7409 |
rs774934498 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6846416 | ACATGGTGAAACCCC[A/G]CCTCTATTAAAAGTA | 7409 |
rs774940644 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795586 | GTCTGAGAACTGATG[A/G]TACGTAACGGTTTAC | 7409 |
rs775027152 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776459 | CCACCCACCCATCCA[C/T]CCACCCATCCATCCA | 7409 |
rs775043505 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793466 | TGTTGGGGGAGCTTA[C/T]GGAGAGAAGAAACAT | 7409 |
rs775051551 | snp | A/G | 1.67497e-05 | 0.00289389 | splice-donor-variant | VAV1 | GRCh38.p7 | 19:6821860 | GTCCGACCAGATCGA[A/G]TGAGTGCTCAGGCCT | 7409 |
rs775081040 | snp | C/G | 4.96052e-05 | 0.00497998 | missense | VAV1 | GRCh38.p7 | 19:6836547 | GCTCACGAAGGCTGA[C/G]GCTGAACAGAACTGG | 7409 |
rs775123713 | snp | C/T | 1.6998e-05 | 0.00291525 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825377 | TGGCGCAGCCAATCT[C/T]TACCAGGTCTTCATC | 7409 |
rs775142821 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6783817 | GGCTCCATTTAACTA[A/C]GAGGGAGACTAGGAA | 7409 |
rs775175030 | snp | A/G | 9.2366e-05 | 0.00679518 | missense | VAV1 | GRCh38.p7 | 19:6826629 | TCCTCGTCTATGGCC[A/G]CTACTGCAGCCAGGT | 7409 |
rs775183200 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807561 | TGGCCCAGTTCCTAA[A/C]AGACCATGGACCGGT | 7409 |
rs775190328 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809119 | AGGGTCTTGTCTTGT[C/T]GCCCAAGCTGGGGTG | 7409 |
rs775206603 | snp | A/G/T | 9.89469e-05 | 0.00703311 | missense | VAV1 | GRCh38.p7 | 19:6850683 | AGATATAACGTCGAG[A/G/T]TCAAGCACATTAAAA | 7409 |
rs775241779 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820473 | CACATTTGTTTAACC[A/G]TTAGTGATTAATTTT | 7409 |
rs775243521 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | VAV1 | GRCh38.p7 | 19:6833743 | AAGAAGGTAAGACTT[C/T]CCCGTGGTCCTTCCT | 7409 |
rs775261017 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801131 | AAGCCCTGTAAGGGC[A/T]GAGCTCTGTTTGTCT | 7409 |
rs775271898 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794927 | GTCACATGATGGGTG[C/T]CTGGGCTGGGATGAC | 7409 |
rs775284726 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775912 | ATGAGAATTCTTCCC[A/C]GTTTCTGTCATTTCT | 7409 |
rs775314955 | snp | A/C | 1.6659e-05 | 0.00288604 | intron-variant | VAV1 | GRCh38.p7 | 19:6848166 | CCTGGGCCCTGCGGG[A/C]CTGGGAAAAAGGGTA | 7409 |
rs775347638 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843951 | GGGCATTGAACAATT[A/G]CTGGCGCATCAGCTA | 7409 |
rs775350839 | snp | A/G | 6.60928e-05 | 0.00574822 | intron-variant | VAV1 | GRCh38.p7 | 19:6821697 | TGAGTAACCACCTGG[A/G]CCTTGGGCCATTTAG | 7409 |
rs775412473 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815072 | GGTCAGAGCCTTGGG[C/T]GAGCAACAGAATCTA | 7409 |
rs775415295 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838057 | GGTGTTCTGCTGCAA[A/G]AAAGAGCTGTCCTTT | 7409 |
rs775419939 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831806 | GTTGAACAGAAAAAT[C/T]GATGATGAGTGACAT | 7409 |
rs775538779 | snp | C/T | 1.64827e-05 | 0.00287073 | intron-variant | VAV1 | GRCh38.p7 | 19:6833658 | GCTGGGAGGTGAGCT[C/T]GGTTCTCTTTGGAGG | 7409 |
rs775606447 | snp | G/T | 1.64836e-05 | 0.0028708 | intron-variant | VAV1 | GRCh38.p7 | 19:6843215 | AGGTTTCTGGGTTGG[G/T]GTTCCAGGCTGGGTA | 7409 |
rs775625377 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824894 | TTCCGCTTTTGGGTT[A/G]TTATGAATAATTTCA | 7409 |
rs775636501 | in-del | -/A | 1.64857e-05 | 0.00287099 | frameshift-variant | VAV1 | GRCh38.p7 | 19:6857072 | GGCTGGTTCCCTGCC[-/A]ACTACGTGGAGGAAG | 7409 |
rs775646309 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810303 | CTACTGCACTTCAGC[C/G]TGGGCAACAGAGTGA | 7409 |
rs775650323 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808964 | GCCTGAGTGCTTGAA[-/T]TTGGCAGGAGTATTC | 7409 |
rs775726642 | in-del | -/T/TT | 0.0367124 | 0.130628 | intron-variant | VAV1 | GRCh38.p7 | 19:6833151 | AAAATACTGACCTTC[-/T/TT]TTTTTTTTTTTTTTT | 7409 |
rs775744876 | snp | C/T | 1.70243e-05 | 0.00291751 | intron-variant | VAV1 | GRCh38.p7 | 19:6825170 | GTCTAGTGCGGATAA[C/T]CTGCTGCCCCTACCT | 7409 |
rs775848923 | snp | A/G | 1.65023e-05 | 0.00287244 | intron-variant | VAV1 | GRCh38.p7 | 19:6828591 | TGGGTCGGCTGTTGG[A/G]GGGCCAGGTTCACCC | 7409 |
rs775929084 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807088 | GAGCAGCAGTCTCCA[A/G]CCTTTTTGGTAGCAG | 7409 |
rs775931605 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830491 | GTTGTTCAGGCTGGA[A/G]TGCAGTGGCACGGTC | 7409 |
rs775953023 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849115 | TTCAACTTATTTTAG[A/C]ATCAGAGGGCACATG | 7409 |
rs775997299 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792264 | AAGTGATGGTGGCCT[C/T]GACTGGGAGTTGGGA | 7409 |
rs776010416 | snp | A/G | 1.70883e-05 | 0.00292299 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6826675 | ACACCTGGACCGTGT[A/G]GCCGCAGCCCGGGAG | 7409 |
rs776028086 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6818098 | GTGCTGGGATTACAG[G/T]TGTGCACCACCACAC | 7409 |
rs776043146 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6822634 | TCCCATCGCTTTTCC[A/T]TTCTGTGACTGTCTC | 7409 |
rs776050462 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824747 | ATCTTGGCCAGGCTG[G/T]TCTTGAACTCCTGAC | 7409 |
rs776054554 | snp | C/T | 1.6701e-05 | 0.00288968 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6822221 | CCTCACAACCCACAG[C/T]GACACGGTGGAGGAG | 7409 |
rs776108211 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831529 | ACATTGGTCAGGCTG[A/G]TCTCAAACTCCTGAC | 7409 |
rs776117196 | snp | C/T | 1.69238e-05 | 0.00290888 | intron-variant | VAV1 | GRCh38.p7 | 19:6853910 | TGAGTGGGTATCTGC[C/T]CCAGACCCTTTTCTC | 7409 |
rs776120257 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6803085 | CTAAATTGGGGCTCA[A/G]CCTGGGACGGTTCTT | 7409 |
rs776184158 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832512 | CTCCTTCTCCTTTCC[C/T]CCTCCTCTTTCCTCC | 7409 |
rs776213387 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815535 | TTAAAGTTCATGTTC[A/C]ATATGCAATGGGTTG | 7409 |
rs776228118 | snp | A/G | 1.64768e-05 | 0.00287021 | intron-variant | VAV1 | GRCh38.p7 | 19:6837072 | GCCTCAAGTCTGAAT[A/G]GAATAAGGGCAAGGG | 7409 |
rs776248080 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810960 | AAGGCATGCTTTCAA[C/T]TGTTGTTCCAAAACC | 7409 |
rs776253761 | snp | A/G | 3.32452e-05 | 0.00407695 | intron-variant | VAV1 | GRCh38.p7 | 19:6850779 | GTCAATGTCCGCTCA[A/G]TCCCAGCTTTCCAGA | 7409 |
rs776266336 | in-del | -/CTT | 4.25971e-05 | 0.00461484 | intron-variant | VAV1 | GRCh38.p7 | 19:6833148 | GAATAAAATACTGAC[-/CTT]CTTTTTTTTTTTTTT | 7409 |
rs776283092 | snp | C/G/T | 0.0035534 | 0.0420189 | intron-variant | VAV1 | GRCh38.p7 | 19:6833153 | AAATACTGACCTTCT[C/G/T]TTTTTTTTTTTTTTA | 7409 |
rs776311282 | snp | A/C | 1.67826e-05 | 0.00289673 | missense | VAV1 | GRCh38.p7 | 19:6821802 | CCAGGCCCTTCCCCA[A/C]CGAGGAGGAGAGTGT | 7409 |
rs776315915 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794542 | AGGATAACCAGATGG[G/T]TGTGGTGTCAAGAGA | 7409 |
rs776369319 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786733 | GGTTGCAGTGAACCA[C/T]GATTGCACCACTGCA | 7409 |
rs776385547 | snp | A/C | 1.65307e-05 | 0.0028749 | intron-variant | VAV1 | GRCh38.p7 | 19:6821705 | CACCTGGGCCTTGGG[A/C]CATTTAGCCCCAGTC | 7409 |
rs776439714 | snp | C/T | | | synonymous-codon | VAV1 | GRCh38.p7 | 19:6843149 | GGGCCCTCCTCAGGA[C/T]CTGTCTGTTCATCTC | 7409 |
rs776489687 | in-del | -/ATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776406 | TCCACCCACCCATCT[-/ATCC]ATCCATCCATCCATC | 7409 |
rs776494975 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797364 | GAATAGTTTGAATTA[C/T]AAAGAATACAAATTT | 7409 |
rs776507975 | snp | A/C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788608 | TCTTGAATGACCTCA[A/C/T]GTGATCTGCCCACCT | 7409 |
rs776534055 | in-del | -/ATCTATCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855839 | TCTATCTATCTATCT[-/ATCTATCC]ATTCATTATCTATCT | 7409 |
rs776566167 | snp | A/T | | | downstream-variant-500B | VAV1 | GRCh38.p7 | 19:6857658 | CAACTTGAATCTGGG[A/T]TATGAAATTCCCTCT | 7409 |
rs776603747 | in-del | -/AA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797233 | TGAGACTCAGTATCA[-/AA]AAAAAAAAAAAAAAA | 7409 |
rs776694939 | in-del | -/TGCCGGGTGC | 1.67391e-05 | 0.00289297 | frameshift-variant | VAV1 | GRCh38.p7 | 19:6772847 | CACTGGCTCATCCAG[-/TGCCGGGTGC]TGCCGCCCAGCCACC | 7409 |
rs776706704 | snp | A/T | 1.65206e-05 | 0.00287403 | intron-variant | VAV1 | GRCh38.p7 | 19:6829735 | CTGGTCAGAGGGCTG[A/T]TGGGGACAGTTGGGA | 7409 |
rs776710563 | snp | C/T | 1.71185e-05 | 0.00292557 | missense | VAV1 | GRCh38.p7 | 19:6833550 | TTCTATCAGGGCTAC[C/T]GCTGCCATCGGTGCC | 7409 |
rs776744161 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796449 | TTCCTCCCTCCCCCT[C/T]GCTTACTCTGCTCCA | 7409 |
rs776758044 | snp | A/G | 3.29832e-05 | 0.00406085 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825082 | CCTGCAACGGTTCCT[A/G]AAACCTCAAGACATT | 7409 |
rs776808200 | in-del | -/CCA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838431 | CATCCATCCATCCAT[-/CCA]TCCATCTATCATCTA | 7409 |
rs776815420 | snp | A/G | 1.72653e-05 | 0.00293809 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6848004 | TCTTTGCAGGTACGC[A/G]GGCCCCATGGAGCGG | 7409 |
rs776823185 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6810078 | CCAACACTCAGGAGG[C/T]TGAGGCAAGAGGATC | 7409 |
rs776828202 | snp | A/C | 1.64991e-05 | 0.00287215 | missense | VAV1 | GRCh38.p7 | 19:6828467 | AAGGAGAACCTGCGG[A/C]TGGCCCTGGATGCCA | 7409 |
rs776830341 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781250 | GACGTTTTATTTTGT[C/G]AACCGAAGTGCTAGC | 7409 |
rs776845862 | snp | A/G | 1.66139e-05 | 0.00288213 | intron-variant | VAV1 | GRCh38.p7 | 19:6828181 | CTCCAGGTGCCAGGC[A/G]CATCTCTAGGCGTGG | 7409 |
rs776870760 | snp | A/G | 1.64741e-05 | 0.00286998 | missense | VAV1 | GRCh38.p7 | 19:6820738 | AGAACCTTCCTGTCC[A/G]CCTGCTGTGAGAAGT | 7409 |
rs776886110 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | VAV1 | GRCh38.p7 | 19:6828604 | GGGGGGCCAGGTTCA[C/T]CCCTGCCCCCTCCCC | 7409 |
rs776894914 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802720 | AGTGTGGTTCAAAGA[C/G]GCAGTGTTGTACAGA | 7409 |
rs776898822 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840521 | AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT | 7409 |
rs776946455 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809287 | CTTTGTTGCCAGGCT[A/G]GTCTTGAACTCCTGG | 7409 |
rs776987173 | snp | G/T | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771955 | TGGAATGCGGAAAAG[G/T]CTGTGATTTGAAATG | 7409 |
rs777010089 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6790928 | CCATGTTTTATGGAG[A/G]GGCACTTTTGCCTCT | 7409 |
rs777010837 | snp | C/T | 1.68963e-05 | 0.00290652 | intron-variant | VAV1 | GRCh38.p7 | 19:6822335 | GTCCATGCCGGTGCG[C/T]GACGTGGAGGGTCGG | 7409 |
rs777012664 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791412 | CTAGCTCCTCATCTC[A/G]AGGTCCTTGAGCTAT | 7409 |
rs777063893 | snp | A/C | 9.72337e-05 | 0.0069719 | synonymous-codon, intron-variant | VAV1 | GRCh38.p7 | 19:6822466 | CTGCCTGCGGGAGAT[A/C]CAGCAGACGGAGGAG | 7409 |
rs777064585 | snp | A/G | 1.67472e-05 | 0.00289367 | missense | VAV1 | GRCh38.p7 | 19:6772845 | CCCACTGGCTCATCC[A/G]GTGCCGGGTGCTGCC | 7409 |
rs777187926 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6808724 | GTGTAACAAACAGTC[C/T]CCTAAAATGGAATGG | 7409 |
rs777210532 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839561 | GCGTGAGCCACCACG[A/C]CCGGCTGGGTATGGC | 7409 |
rs777227420 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776936 | CTAATTTTATATTTT[C/T]AGTAGAGATGGGGTT | 7409 |
rs777231436 | in-del | -/AGA | 8.24029e-05 | 0.00641831 | cds-indel | VAV1 | GRCh38.p7 | 19:6850709 | TAAAATCATGACAGC[-/AGA]AGGACTGTACCGGAT | 7409 |
rs777250984 | snp | A/G | 1.6698e-05 | 0.00288941 | intron-variant | VAV1 | GRCh38.p7 | 19:6836595 | GGCCACAAGAGTGAT[A/G]GGGTGGGACCCAAGT | 7409 |
rs777282437 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775615 | GTACCCAGACCCTTT[C/T]CCTCTTCGAGGGGGC | 7409 |
rs777340589 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798617 | AGGATTGCACCACTG[C/T]ACTCCAGTCTGGGTG | 7409 |
rs777366043 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800791 | ACGCCTGGCAAATTT[-/G]TTGTGTGTGTGTGTG | 7409 |
rs777449559 | in-del | -/ACT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832666 | CTTCCTCCTCCTCCT[-/ACT]CCTCTTCCTCCTCTT | 7409 |
rs777455892 | in-del | -/GAA | 1.64966e-05 | 0.00287194 | cds-indel | VAV1 | GRCh38.p7 | 19:6832165 | CAAGACAAGAGAATT[-/GAA]GAAGAAGTGGATGGA | 7409 |
rs777470345 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837796 | AGTGAGTTTGCAGAC[A/G]ACGTTCCCCTTTACC | 7409 |
rs777477520 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799583 | CATTAGGTATTTCTC[C/G]GAATGCTATCCCTCT | 7409 |
rs777481090 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840134 | CACCTATTCCCCTCT[C/G]CCAGCCCCTGACATT | 7409 |
rs777502939 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773555 | GGGGCAGGTGGGGGG[-/C]TGCAGCCCCAGGGAT | 7409 |
rs777506541 | snp | A/G/T | 3.30465e-05 | 0.00406477 | synonymous-codon, missense | VAV1 | GRCh38.p7 | 19:6828430 | TCAGGAGCTGGTGAA[A/G/T]CACACGCAGGAGGCG | 7409 |
rs777525198 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850887 | CTACAGTGCAAGTGA[C/T]CTTAAACTTATGCTC | 7409 |
rs777545770 | snp | C/T | 1.67181e-05 | 0.00289115 | intron-variant | VAV1 | GRCh38.p7 | 19:6836404 | GTTGACTGCCAACCA[C/T]CCTGTACTCCTGTAC | 7409 |
rs777550036 | snp | A/C | 1.64743e-05 | 0.00287 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6854025 | CAGAGCTGTCGCTCA[A/C]GGAGGGTGACATCAT | 7409 |
rs777609928 | snp | G/T | 1.68074e-05 | 0.00289887 | intron-variant | VAV1 | GRCh38.p7 | 19:6832203 | TTGAGATGGCCATGT[G/T]AGTCCCCGTCTTCCT | 7409 |
rs777610860 | snp | A/C | 1.65026e-05 | 0.00287246 | intron-variant | VAV1 | GRCh38.p7 | 19:6828574 | GGGATTAGGTAGGAG[A/C]CTGGGTCGGCTGTTG | 7409 |
rs777613865 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6781104 | ATGGGGGTCTCACCA[C/T]GTTGCCCAGGCTGGT | 7409 |
rs777650310 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849439 | GATTTACAGGTGCAC[A/G]TCACCATGCCTGGCT | 7409 |
rs777672563 | snp | C/T | 1.651e-05 | 0.0028731 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6836511 | ACCCTTTCTACGGCT[C/T]AACCCTGGAGACATT | 7409 |
rs777680501 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6788585 | TTTCACCAGATTGGC[C/T]AGGCTGGTCTTGAAT | 7409 |
rs777740319 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806332 | CCTTGTGATTCACCC[A/G]CCATGGGCTCCCAAA | 7409 |
rs777740563 | snp | A/C | 1.65042e-05 | 0.0028726 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821663 | CTGGACCCCGATCGC[A/C]CAGAACAGGGGGATC | 7409 |
rs777816861 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785120 | GATTTCTCTTCCCTC[-/A]GGTATACACGGTGAG | 7409 |
rs777856537 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6828117 | GAGGTTCACCCTGCG[A/G]GACCTGCTGATGGTG | 7409 |
rs777937518 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824207 | TGGCCTCCCAAAGTG[-/T]TGGGATTTTGGGTGT | 7409 |
rs778005051 | snp | A/G | 1.65337e-05 | 0.00287517 | intron-variant | VAV1 | GRCh38.p7 | 19:6850761 | CGGGGGCTTACGGTA[A/G]GGGTCAATGTCCGCT | 7409 |
rs778029269 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813270 | AGCTTCAGCTCCTCT[C/T]CACCTGGGGCTCCCC | 7409 |
rs778062725 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840384 | AATCTTGGCTCACTG[C/T]AAGCTCCACTTCCCG | 7409 |
rs778088852 | snp | A/C | 1.68088e-05 | 0.00289899 | intron-variant | VAV1 | GRCh38.p7 | 19:6825138 | TGAGCCGGCCGATCC[A/C]CAGCCCTCTTGGGTC | 7409 |
rs778093830 | snp | A/G | 3.35785e-05 | 0.00409733 | intron-variant | VAV1 | GRCh38.p7 | 19:6828918 | GGGTGGAGTCAACAT[A/G]GATCTGGGATGGAGC | 7409 |
rs778167211 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6823275 | GGATTACAGGCATGC[A/G]CCACCATGCTCGACT | 7409 |
rs778250359 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830143 | GGCTCACCGCAACCT[C/T]CGCCTCCTGGGTTCA | 7409 |
rs778283056 | in-del | -/ATTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6787593 | TTTATTTATTTATTT[-/ATTT]ATTTATTTATTTATT | 7409 |
rs778293852 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6834282 | GGAGTCTTGCTGTGT[C/T]GCCCAGGCTGGAGTG | 7409 |
rs778321882 | snp | A/G | 1.65798e-05 | 0.00287917 | missense | VAV1 | GRCh38.p7 | 19:6833610 | AGGGTCCCTCCATGT[A/G]GCCGACATGGGCAAG | 7409 |
rs778372936 | snp | C/G | 0.00023092 | 0.0107428 | intron-variant | VAV1 | GRCh38.p7 | 19:6828724 | GTGAGGCGGTGGAGC[C/G]GGGTGGGCCAGGGGT | 7409 |
rs778399512 | snp | A/T | 1.6477e-05 | 0.00287024 | missense | VAV1 | GRCh38.p7 | 19:6854051 | ATCATCAAGATCCTT[A/T]ACAAGAAGGGACAGC | 7409 |
rs778405371 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786461 | AGCAAGCCCGTCCCT[A/G]TAAAATAAATTAATT | 7409 |
rs778414712 | snp | C/T | 3.31686e-05 | 0.00407225 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6825306 | CCCTCCGAGTAGGAC[C/T]TGCTTCGTGTTCATA | 7409 |
rs778426100 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6802346 | AAAGTATAATAATAA[C/T]AAAATTAAAAAAAAT | 7409 |
rs778476573 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6795460 | TTGCTTCACCCAGGG[C/T]GTAGTTCTTTTATTT | 7409 |
rs778520862 | snp | C/G | 1.65059e-05 | 0.00287275 | intron-variant | VAV1 | GRCh38.p7 | 19:6828583 | TAGGAGCCTGGGTCG[C/G]CTGTTGGGGGGCCAG | 7409 |
rs778524498 | snp | C/T | 1.65113e-05 | 0.00287322 | missense | VAV1 | GRCh38.p7 | 19:6836525 | TCAACCCTGGAGACA[C/T]TGTGGAGCTCACGAA | 7409 |
rs778528187 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796966 | TATTTGGCCAGGCAC[A/G]GTGGCTCACATCTGT | 7409 |
rs778537717 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6824516 | TGAATAATATTCCAT[C/T]GTATGGATGGACCAC | 7409 |
rs778561140 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847582 | TCATTTACCTTGATG[A/C]CTAGGTTTTTTGGCT | 7409 |
rs778599065 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785920 | CGTCTCGGCCTCCCA[A/G]AGTGCTGGGATTACA | 7409 |
rs778633447 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848980 | TATATTTTTTGTAGA[A/G]ACGAGGGTCTCTCCT | 7409 |
rs778685554 | snp | A/C | 1.69037e-05 | 0.00290716 | intron-variant | VAV1 | GRCh38.p7 | 19:6832208 | ATGGCCATGTGAGTC[A/C]CCGTCTTCCTCCCTC | 7409 |
rs778756366 | snp | C/G | | | | | GRCh38.p7 | 19:6784472 | GCACTTGGCACCATC[C/G]CTTTCCATTCCATTC | 7409 |
rs778776109 | snp | A/G | 6.58903e-05 | 0.00573941 | intron-variant, synonymous-codon | VAV1 | GRCh38.p7 | 19:6836996 | TTAGGGCAGAAATAC[A/G]TCTACTAATGAAATT | 7409 |
rs778776855 | snp | C/G | 0.000507485 | 0.0159212 | intron-variant | VAV1 | GRCh38.p7 | 19:6822389 | GGCAGCCCCAGGCCC[C/G]CCAACACCGGCCTCT | 7409 |
rs778809962 | snp | A/G | 2.20427e-05 | 0.00331977 | intron-variant | VAV1 | GRCh38.p7 | 19:6833137 | GCCATAAAAAGGAAT[A/G]AAATACTGACCTTCT | 7409 |
rs778813868 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782018 | CTGATTGTCTTATCT[A/G]TAAAACAGGAAATCT | 7409 |
rs778880027 | snp | A/C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6801672 | GGTAACAGGCATTTC[A/C/G]GGTTTCCGGCCGGCT | 7409 |
rs778894622 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6791732 | CACATTGTAATAAAT[A/G]TCACAGATGAAACAA | 7409 |
rs778941064 | snp | A/G | 0.000134275 | 0.00819266 | intron-variant | VAV1 | GRCh38.p7 | 19:6821882 | CTCAGGCCTGTGGCC[A/G]CACAGCTCACTGGAG | 7409 |
rs778943583 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780676 | TCCTGGGTTCAAGAG[-/A]TTCTCCTGCCTCAGC | 7409 |
rs778963741 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6854302 | GCTGTGTGCAGACAT[C/T]GTGCTGGGTGTCGAG | 7409 |
rs778985784 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6813241 | TCTACTTCCTGAGTG[G/T]CTGGGCCACATAGAG | 7409 |
rs778992376 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785252 | TCATAGCTCACTGCA[A/G]CCTCCAACTTCTGGG | 7409 |
rs779040297 | in-del | -/AAA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6797232 | GTGAGACTCAGTATC[-/AAA]AAAAAAAAAAAAAAA | 7409 |
rs779063068 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6827870 | CTCCCAAAGTTCCTT[C/T]CAGTGGTTCTCAAGC | 7409 |
rs779102173 | in-del | -/TCCTCCTCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832663 | CCTTCTTCCTCCTCC[-/TCCTCCTCT]TCCTCCTCTTCTTTC | 7409 |
rs779109227 | in-del | -/ATAG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6851160 | TTTATTTTTATATAT[-/ATAG]ATAGATAGAGAGAGA | 7409 |
rs779118085 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6840166 | ACATTCTACTCTTGA[G/T]CTCTATGGATTTTTC | 7409 |
rs779142587 | snp | A/G | 3.29511e-05 | 0.00405887 | intron-variant | VAV1 | GRCh38.p7 | 19:6833866 | CCTACAAGCCCCCAG[A/G]CTGGGCATAGGTAGA | 7409 |
rs779219530 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820206 | TGACTGAAGTCCTAG[C/T]TACCTGGGAGGTGGA | 7409 |
rs779222036 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | VAV1 | GRCh38.p7 | 19:6820675 | CCTTTCGTACTGCCC[C/T]ACCCTCATTTCTCTG | 7409 |
rs779237233 | snp | G/T | 1.69226e-05 | 0.00290878 | intron-variant | VAV1 | GRCh38.p7 | 19:6825156 | GCCCTCTTGGGTCTG[G/T]CTAGTGCGGATAACC | 7409 |
rs779239283 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784290 | TCTGTGGAAATCTCA[A/G]TGGGATGTAGAATAA | 7409 |
rs779265186 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6829876 | AAACCTGCACAGCTT[C/T]CAGGTTCGGGATGAC | 7409 |
rs779267318 | snp | C/G | 1.64882e-05 | 0.00287121 | intron-variant | VAV1 | GRCh38.p7 | 19:6833986 | GCTGTGTGGGGGCAG[C/G]AGGAAAATTCATCTC | 7409 |
rs779271642 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6825806 | GAGGCGGGTGGATCA[C/T]TTAAGGTGAGGAGTT | 7409 |
rs779293312 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6843457 | GGTAATGACAGTTCC[A/G]GTTGTTTTTGTAGGA | 7409 |
rs779293780 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853136 | CCCATTGTGGAGGGA[A/G]ACTTTGGGGATGCCA | 7409 |
rs779389159 | snp | C/G | 1.65176e-05 | 0.00287376 | intron-variant | VAV1 | GRCh38.p7 | 19:6848119 | ATCAGCATTAAGTAA[C/G]TCCTTTCTCCCTGAC | 7409 |
rs779447710 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6798648 | ACAGAGTGAGACCCT[A/G]TTTCTCCCCTTCCCC | 7409 |
rs779478172 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853645 | CTGAGGCAGGAGAAT[-/C]ACTTGAACCCAGGAG | 7409 |
rs779497236 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6807299 | TTTCCTGCAACTAGA[C/T]GATCCCATCTGGGGG | 7409 |
rs779506427 | snp | C/T | 0.000148286 | 0.00860936 | intron-variant | VAV1 | GRCh38.p7 | 19:6825026 | GGGAATCTTATCTTC[C/T]GTCATCTTTCTCTCC | 7409 |
rs779532513 | snp | C/T | 6.59055e-05 | 0.00574007 | intron-variant | VAV1 | GRCh38.p7 | 19:6820832 | AGGTGAGCTGCACAC[C/T]TGAAGCCCAAAGACT | 7409 |
rs779560082 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809593 | GAAGTCAGCAGGGGC[C/T]GTGGTGAGGTTGAAC | 7409 |
rs779560365 | snp | A/T | 1.65351e-05 | 0.00287528 | missense | VAV1 | GRCh38.p7 | 19:6828880 | GATCACCTCGGTGGA[A/T]CGGCGCTCCAAGATG | 7409 |
rs779571766 | snp | C/T | 4.94214e-05 | 0.00497074 | intron-variant, synonymous-codon | VAV1 | GRCh38.p7 | 19:6837047 | GGTGAAGCCCTATGT[C/T]CATGTGAGTGCCTCA | 7409 |
rs779625156 | snp | C/T | 0.000785054 | 0.0197967 | intron-variant | VAV1 | GRCh38.p7 | 19:6833148 | GAATAAAATACTGAC[C/T]TTCTTTTTTTTTTTT | 7409 |
rs779637079 | snp | C/T | 0.000100568 | 0.00709042 | intron-variant | VAV1 | GRCh38.p7 | 19:6822413 | GGCCTCTCCCCTCGC[C/T]CTCAGCCCAAGATGA | 7409 |
rs779641231 | snp | G/T | 8.24178e-05 | 0.00641889 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772936 | GGATGGTGTCCTTCT[G/T]TGTCAGCTGCTTAAC | 7409 |
rs779669403 | snp | A/G | 1.64882e-05 | 0.00287121 | missense, synonymous-codon | VAV1 | GRCh38.p7 | 19:6854069 | AAGAAGGGACAGCAA[A/G]GCTGGTGGCGAGGGG | 7409 |
rs779697064 | in-del | -/GAGACTCCGTCTCAAAAAAAAAAAAAGAA | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771729 | CCTGGGTGACAGAGT[lengthTooLong]GAAAGAAACAAAGAG | 7409 |
rs779722438 | snp | A/T | 3.30382e-05 | 0.00406423 | intron-variant | VAV1 | GRCh38.p7 | 19:6857012 | AGGGGCAGTAGGAGG[A/T]TGTGCAGAGGTTGCA | 7409 |
rs779730959 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776190 | CCATCCATCCATCCA[-/C]TCCACTCCTCCATCC | 7409 |
rs779765188 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6821316 | TGAGGCAGGAGAATC[G/T]CTTGAACCTGGGAGG | 7409 |
rs779797755 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6817134 | GCTCACTGCAACCTC[C/T]GCCTCCTGGTTCAAG | 7409 |
rs779801032 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777109 | ATCCATCCATCTACT[-/CATC]CATCCATCCATCCAT | 7409 |
rs779809203 | snp | C/T | 4.94205e-05 | 0.0049707 | missense | VAV1 | GRCh38.p7 | 19:6843142 | ATTCTTAGGGCCCTC[C/T]TCAGGACCTGTCTGT | 7409 |
rs779830703 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804132 | GTGAAAATACTCTCT[A/G]TGACACTATAATAGT | 7409 |
rs779845211 | snp | C/T | 3.32535e-05 | 0.00407746 | utr-variant-3-prime | VAV1 | GRCh38.p7 | 19:6857154 | TCCAGGCTCTGAGCC[C/T]GGCGTGGGCAGGCAG | 7409 |
rs779904890 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784840 | TTGGTCCAGTGCTGG[A/G]AAATGTCACCTTTCA | 7409 |
rs779910201 | snp | A/G | 1.64838e-05 | 0.00287083 | missense | VAV1 | GRCh38.p7 | 19:6828145 | GTGCCTATGCAGCGA[A/G]TTCTCAAATATCACC | 7409 |
rs779933732 | snp | C/T | 1.69069e-05 | 0.00290743 | intron-variant | VAV1 | GRCh38.p7 | 19:6833174 | TTTTTTTTTAATTTT[C/T]CCCTGCCAGCTCCAA | 7409 |
rs780005009 | in-del | -/TTAAT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6786206 | ATAGTACGGAATCAA[-/TTAAT]TTAATTTATTCATTT | 7409 |
rs780011460 | snp | C/T | 3.31923e-05 | 0.0040737 | intron-variant | VAV1 | GRCh38.p7 | 19:6850773 | GTAAGGGTCAATGTC[C/T]GCTCAATCCCAGCTT | 7409 |
rs780024343 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811594 | AGATGGGCCTTGAAG[C/G]ATGAGTAGGAGTTCA | 7409 |
rs780031060 | snp | A/G | 1.66466e-05 | 0.00288496 | intron-variant | VAV1 | GRCh38.p7 | 19:6828380 | CCGCAGGGAGAAGGG[A/G]AGGGGCCCAGGTGAC | 7409 |
rs780032946 | snp | A/C/T | 6.71282e-05 | 0.00579314 | intron-variant | VAV1 | GRCh38.p7 | 19:6821783 | CTCACACCCTCCTGA[A/C/T]CCCCCAGGCCCTTCC | 7409 |
rs780084625 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6820168 | TACAAAAAATACAGA[A/G]ATTAGCTGGGTGTTG | 7409 |
rs780187115 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799978 | ATGGAATATATCGTA[C/T]GATAGGTGCATGCTT | 7409 |
rs780261774 | snp | C/T | 1.6489e-05 | 0.00287128 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6832147 | GGGCTATGAGCTGTT[C/T]TTCAAGACAAGAGAA | 7409 |
rs780316145 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6794912 | TCTGGAGGATTCTTC[A/G]TCACATGATGGGTGT | 7409 |
rs780355047 | in-del | -/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6772091 | AAAGGCCCTGGGGCA[-/G]GGCCGTATGTTCCTG | 7409 |
rs780355067 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804096 | GTATGGATAGGCAGA[A/G]CATGGAAGCTTTCCA | 7409 |
rs780372507 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831336 | TTCTTTTTTTGAGAC[A/G]GAGCCTCGCTCTGTC | 7409 |
rs780416467 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800693 | GTGGCGTGATCTCGG[A/C]TCACTGCCACCTCCG | 7409 |
rs780425645 | in-del | AGCCTTTTTTTTT/CAGCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6774424 | TGAGCCACCGCGCCC[AGCCTTTTTTTTT/CAGCC]TTTTTTTTTTTTTTT | 7409 |
rs780465487 | in-del | -/CCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832669 | CCTCCTCCTCCTCCT[-/CCC]CTTCCTCCTCTTCTT | 7409 |
rs780472452 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6811663 | GTCCTTTATTCATCT[C/G]CCTGCATATAATTAC | 7409 |
rs780486477 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806278 | TTTTAGTAGAAACGG[A/G]GTTTCACCATGTTGG | 7409 |
rs780489736 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6820704 | TGTCTCCTCACAGTT[C/T]CTGTGCCTTAAGAAC | 7409 |
rs780542764 | snp | A/T | 3.29592e-05 | 0.00405938 | intron-variant | VAV1 | GRCh38.p7 | 19:6820845 | ACTTGAAGCCCAAAG[A/T]CTGAGTTTCAGTTAA | 7409 |
rs780600888 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779939 | ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 7409 |
rs780636360 | in-del | -/CA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777342 | GGACAGTGGGAATAG[-/CA]CACACACACAAAAAC | 7409 |
rs780663813 | snp | A/C | 0.000181841 | 0.00953348 | intron-variant | VAV1 | GRCh38.p7 | 19:6773036 | CCGCGGGCAGGTGTG[A/C]TGAGGGTTGGAGACG | 7409 |
rs780665383 | snp | A/G | 6.59761e-05 | 0.00574314 | missense | VAV1 | GRCh38.p7 | 19:6821631 | TCACAGGTCATCTAC[A/G]CCCTGTCTGCTCTGT | 7409 |
rs780696439 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777002 | CCTTGTGATCCACTC[A/G]CCTCAGCCTTCCAAA | 7409 |
rs780707542 | snp | A/G | 0.000233038 | 0.0107919 | utr-variant-3-prime | VAV1 | GRCh38.p7 | 19:6857158 | GGCTCTGAGCCCGGC[A/G]TGGGCAGGCAGCGGA | 7409 |
rs780725542 | snp | A/C | 1.64825e-05 | 0.00287071 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6772972 | GCTACCCCATGCCAT[A/C]AACCTGCGTGAGGTC | 7409 |
rs780749744 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789630 | TCTGATGGAGTCTCT[C/T]TCTGTCACTCAGACT | 7409 |
rs780780295 | in-del | -/AC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835217 | TATATATATACATAC[-/AC]ACACACACACACACA | 7409 |
rs780787883 | in-del | -/CA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6815729 | CTGTGTGTCTCACCT[-/CA]GTTTCCTTCTCTGTA | 7409 |
rs780827407 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6839295 | CTGGGCTCAAGCAAT[C/T]CTCTCATAGAACATC | 7409 |
rs780887815 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6826470 | ACATGGGAGATGCTA[C/T]TGTTATGCCCATTTC | 7409 |
rs780975522 | snp | C/T | 8.32064e-05 | 0.00644952 | intron-variant | VAV1 | GRCh38.p7 | 19:6852955 | ATCTGCCATGTGGTC[C/T]GCCTTCTAGGAGCTG | 7409 |
rs780976071 | snp | C/T | 1.66335e-05 | 0.00288383 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6833190 | CCCTGCCAGCTCCAA[C/T]ATCTATCCGGAGAAT | 7409 |
rs780976179 | snp | C/G | 1.78029e-05 | 0.00298348 | intron-variant | VAV1 | GRCh38.p7 | 19:6847961 | GGGACCCAGGCACGG[C/G]GACCGTGCCACCTCT | 7409 |
rs781029066 | snp | A/G | 1.65589e-05 | 0.00287736 | intron-variant | VAV1 | GRCh38.p7 | 19:6833291 | TGCTGCTTAGGTGAG[A/G]ATCTGGGAGGAGGGT | 7409 |
rs781036171 | snp | C/T | 1.67815e-05 | 0.00289663 | intron-variant | VAV1 | GRCh38.p7 | 19:6836383 | TGGCAAGATTCAGGG[C/T]TGAAAGTTGACTGCC | 7409 |
rs781046322 | snp | G/T | 1.65564e-05 | 0.00287714 | missense | VAV1 | GRCh38.p7 | 19:6822280 | ATGAGGAGGCGGAAG[G/T]CGACGAGATCTATGA | 7409 |
rs781062800 | in-del | -/ATCT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855807 | TCCACCCATTCATCT[-/ATCT]ATCTATCTATCTATC | 7409 |
rs781062965 | snp | C/T | 4.97187e-05 | 0.00498567 | intron-variant | VAV1 | GRCh38.p7 | 19:6828404 | AGGTGACGTCTGACG[C/T]CTTGGTTCTCTCAGG | 7409 |
rs781065720 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6837885 | AGACACAAAATTCAA[C/T]ATTGACATTATACTA | 7409 |
rs781071437 | in-del | -/T | 5.00463e-05 | 0.00500206 | intron-variant | VAV1 | GRCh38.p7 | 19:6852953 | GCATCTGCCATGTGG[-/T]CCGCCTTCTAGGAGC | 7409 |
rs781099209 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819094 | GCACTCCAGCCTGGC[A/G]GACAAAGTGAGACTC | 7409 |
rs781106679 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804402 | TCAGGGCAGTTTGGC[A/G]GTCCTATTTATATTT | 7409 |
rs781106706 | snp | C/G | 1.72985e-05 | 0.00294091 | intron-variant | VAV1 | GRCh38.p7 | 19:6853109 | ACTGGGGGCTTACAG[C/G]CTCAGCCCCTTCCCA | 7409 |
rs781150286 | snp | A/G | 9.44778e-05 | 0.00687241 | intron-variant | VAV1 | GRCh38.p7 | 19:6826608 | GCCTGTCTTCTCCCT[A/G]TAGGTTCCTCGTCTA | 7409 |
rs781150372 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6821722 | ATTTAGCCCCAGTCC[G/T]CCCCCTCCCTGAAGC | 7409 |
rs781159708 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6799656 | CCTTGGTTGAGGTTT[C/G]AATTACTGATGGCAC | 7409 |
rs781188420 | snp | C/T | 1.64749e-05 | 0.00287005 | intron-variant | VAV1 | GRCh38.p7 | 19:6833902 | TTTCTTTGTTTCTCC[C/T]TCCAGGACAAACTAC | 7409 |
rs781218620 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831168 | TACCTCCATTGTTCA[A/G]GGACATTCTCTGTGG | 7409 |
rs781245406 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819888 | TTTCTTTTTCTTTTT[C/G]CAGATACTCAAAAGC | 7409 |
rs781263339 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6806127 | AGTCTCACTCTGTCA[C/T]CCAGCCTGGAGTACA | 7409 |
rs781263866 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6819051 | AACCTGGGAGGTGGA[A/G]GTTGCAGTGAGCTAA | 7409 |
rs781264116 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782455 | ATGAAATTCCCAGCA[C/T]GGCAATTAACATATA | 7409 |
rs781382160 | in-del | -/TC | 0.000529845 | 0.0162678 | intron-variant | VAV1 | GRCh38.p7 | 19:6828411 | GTCTGACGTCTTGGT[-/TC]TCTCAGGAGCTGGTG | 7409 |
rs781390146 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6792942 | AGCGCTGAGACCGAG[A/G]GACTCAGTGCTAGGC | 7409 |
rs781419385 | in-del | -/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793339 | ACTCCATCTCAAAAA[-/G]AAAGAAAGAAAGAAA | 7409 |
rs781448453 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6777067 | CCCATCCATTCATCT[A/G]TCTATCATCCACCTG | 7409 |
rs781481384 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6830308 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 7409 |
rs781495214 | snp | A/G | 4.94482e-05 | 0.00497209 | intron-variant | VAV1 | GRCh38.p7 | 19:6820855 | CAAAGACTGAGTTTC[A/G]GTTAATTTCTATTGA | 7409 |
rs781520756 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6857046 | ATGAACTCCTCGTCT[A/G]TTTCCAGGTTGGCTG | 7409 |
rs781522310 | snp | C/G | 1.65179e-05 | 0.00287379 | intron-variant | VAV1 | GRCh38.p7 | 19:6833635 | GGCAAGGTACGAGTG[C/G]GAGGGAGGCTGGGAG | 7409 |
rs781567864 | snp | A/G | 1.64898e-05 | 0.00287135 | intron-variant | VAV1 | GRCh38.p7 | 19:6828753 | GTGTGGCCACGTGGG[A/G]AGAGTGTGTGTCTGG | 7409 |
rs781574126 | snp | A/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6855737 | TTCATCCATCCATCC[A/C]TCCGACCACCATCCA | 7409 |
rs781588848 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6796906 | TGTATCTCCAGCACC[A/T]AGACCAGTACTGGGT | 7409 |
rs781603027 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775544 | TAAATAGGAGTTTTT[-/C]TCATTGTTCTGGCTT | 7409 |
rs781609985 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6773452 | AACATCTTCCCCCAC[A/G]TGTGTCTCCTCCTCC | 7409 |
rs781617190 | snp | A/C | 1.66921e-05 | 0.00288891 | intron-variant | VAV1 | GRCh38.p7 | 19:6828909 | TGGACAGGTGGGTGG[A/C]GTCAACATGGATCTG | 7409 |
rs781618198 | snp | C/T | 1.64977e-05 | 0.00287203 | synonymous-codon | VAV1 | GRCh38.p7 | 19:6821643 | TACACCCTGTCTGCT[C/T]TGTCCTGGACCCCGA | 7409 |
rs781647118 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6775266 | GGCCCCATCTGTTAG[A/G]CCTGGCAGGGAGTCA | 7409 |
rs781711216 | snp | C/T | 1.6477e-05 | 0.00287024 | intron-variant | VAV1 | GRCh38.p7 | 19:6825038 | TTCCGTCATCTTTCT[C/T]TCCCTTCCCCGCAGC | 7409 |
rs781742280 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6785378 | TGTCTATTGTCCAGG[C/T]TGGAGTGCAGTGACA | 7409 |
rs781743671 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800737 | GCGATTCTCCTGCCT[-/C]CAGCCTCCAGAGTAG | 7409 |
rs781745825 | in-del | -/ACACACACAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6805597 | TACACACACACACAC[-/ACACACACAC]ACACACACACACACA | 7409 |
rs781777574 | in-del | -/CCA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6838435 | CATCCATCCATCCAT[-/CCA]TCTATCATCTATCTA | 7409 |
rs796101039 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6849101 | TATATATTTTTTTTT[-/T]CAACTTATTTTAGAA | 7409 |
rs796111662 | multinucleotide-polymorphism | AGTTTTGC/GGTCTCAA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779077 | GTTTTCTGAGACAGG[AGTTTTGC/GGTCTCAA]CTGTCACCCAAGCTG | 7409 |
rs796124027 | in-del | -/CATC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776321 | ATCCATCCATCCATC[-/CATC]TGCTCATCCATTCAT | 7409 |
rs796144973 | in-del | -/AC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6835247 | CACACACACACACAC[-/AC]GTATTTTATTGAGAG | 7409 |
rs796157545 | multinucleotide-polymorphism | AT/GC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779105 | ACCCAAGCTGGAGTA[AT/GC]GTGGTATGATCACAG | 7409 |
rs796214312 | snp | A/G | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771751 | CGTCTCAAAAAAAAA[A/G]AAAGAAGAAAGAAAC | 7409 |
rs796276026 | multinucleotide-polymorphism | CCT/TCC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832560 | TCTTCCTCCTCCTCT[CCT/TCC]TCCTCCCCTTCCTCC | 7409 |
rs796290424 | in-del | -/AAGGAAGG | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771793 | GAAAGGAAAGAAAGA[-/AAGGAAGG]AAGGAAGGAAGGAAG | 7409 |
rs796309494 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6821186 | GTGGGCAGATCACGA[A/G]GTCAGGAGATCGATT | 7409 |
rs796313546 | in-del | -/CCATCCACCCACCCATCCACCCAC | | | intron-variant | VAV1 | GRCh38.p7 | 19:6776440 | CATCCATCCATCCAT[-/CCATCCACCCACCCATCCACCCAC]CCATCCATCCATCCA | 7409 |
rs796314682 | in-del | G/TTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6809084 | TACCTCTCTTTTTTT[G/TTT]TTTTTTTTTTTGAGA | 7409 |
rs796316396 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779029 | CTACAGGTGTGCACC[A/G]GCATACCTGGGTGAT | 7409 |
rs796333689 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814678 | CCTTCCTTCCTTTCT[C/T]TCTTTCTTTCTTTCT | 7409 |
rs796369271 | snp | C/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779092 | GGTCTCAATCTGTCA[C/G]CCAAGCTGGAGTATA | 7409 |
rs796379982 | multinucleotide-polymorphism | AG/GA | | | upstream-variant-2KB | VAV1 | GRCh38.p7 | 19:6771754 | TCAAAAAAAAAAAAA[AG/GA]AGAAAGAAACAAAGA | 7409 |
rs796435540 | in-del | -/TTCCTCCTCCTCGCCCTCCTCTTCCTCTTCCTCCTA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6832571 | CTCTCCTTCCTCCCC[lengthTooLong]TTCCTCCTCCTCGCC | 7409 |
rs796446253 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848797 | AATTTAATTTTATTA[A/T]TATTATTGTTATTTT | 7409 |
rs796459916 | in-del | C/TT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778888 | CTTTTTTTTTTTTTT[C/TT]TTAAGAGACAGAGTT | 7409 |
rs796473141 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780608 | ACGGAGTCTCACTCT[A/G]TTCCTCAGGCTGGAG | 7409 |
rs796503710 | in-del | CACACACA/TG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6836867 | CACACACACACACAC[CACACACA/TG]ACACGAGTGATGGGG | 7409 |
rs796530886 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6848589 | TGTATTTTTAGTAGA[G/T]ACGGGGTTTCTCCAT | 7409 |
rs796576869 | in-del | -/GTGT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6831854 | CTTCTGCAAAGGGGA[-/GTGT]GTGTGTGTGTGTGTG | 7409 |
rs796627638 | in-del | -/C | | | intron-variant | VAV1 | GRCh38.p7 | 19:6778889 | TTTTTTTTTTTTTTT[-/C]CTTAAGAGACAGAGT | 7409 |
rs796711643 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779762 | TCATGCCTATAATCC[C/T]AGCACTTTGGCTTAC | 7409 |
rs796719258 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853799 | AGTACAATTGTGTCC[C/T]CTTACAGTACAGGGC | 7409 |
rs796719700 | in-del | -/TTTT | | | intron-variant | VAV1 | GRCh38.p7 | 19:6784494 | ATTCCATTCTGTTCC[-/TTTT]TTTTTTTTTTTTTTG | 7409 |
rs796763550 | in-del | -/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6804726 | CCTTCCCATACCTCC[-/T]TTTTTTTTTTTTTTT | 7409 |
rs796766717 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6789834 | GAACTCCTGACCTCA[A/G]GTGACCTGCCTGCCT | 7409 |
rs796789928 | in-del | -/A | | | intron-variant | VAV1 | GRCh38.p7 | 19:6853730 | GAGAGACTTTATCTC[-/A]AAAAAAAAAAAAAAG | 7409 |
rs796792594 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6847016 | CCTACCGAGTTCAAG[C/T]GATTCTCTTGCCTCA | 7409 |
rs796817151 | snp | G/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6793450 | TTGGTAAAGGGTGAT[G/T]TGTTGGGGGAGCTTA | 7409 |
rs796871083 | snp | C/T | | | missense | VAV1 | GRCh38.p7 | 19:6836480 | ACGGGCTTCCTCCAC[C/T]CCCTGGAGCCATTGG | 7409 |
rs796872937 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6829021 | GGGCAGGGGCGGGGC[C/T]GGGCTTCTAGATGGA | 7409 |
rs796880148 | multinucleotide-polymorphism | AGC/CAG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6780065 | CAGTGAGCCGAGATC[AGC/CAG]CCACTGCACTCCAGC | 7409 |
rs796899296 | snp | C/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6814691 | CTTTCTTTCTTTCTT[C/T]CTTTCTTTCTTTCTT | 7409 |
rs796947256 | in-del | -/TG | | | intron-variant | VAV1 | GRCh38.p7 | 19:6800809 | GTGTGTGTGTGTGTG[-/TG]CAGTCGGGGTTTCAC | 7409 |
rs796966493 | in-del | GTTTGTCTGTCTGTTTTCT/TTTTTTCCTTAA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779051 | TGGGTGATTTTTTTG[lengthTooLong]AGACAGGGTCTCAAT | 7409 |
rs797011687 | snp | A/G | | | intron-variant | VAV1 | GRCh38.p7 | 19:6779096 | TCAATCTGTCACCCA[A/G]GCTGGAGTATAGTGG | 7409 |
rs797014688 | snp | A/T | | | intron-variant | VAV1 | GRCh38.p7 | 19:6850178 | TTTTTTTCTCAACAT[A/T]TCTAGTGTTTTTTTA | 7409 |
rs797014780 | in-del | -/GA | | | intron-variant | VAV1 | GRCh38.p7 | 19:6782488 | GAGTGCTAAATGAAC[-/GA]GAGTCATTATTTTTG | 7409 |