SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs749567654 | snp | A/G | 0.00010628 | 0.00728894 | missense, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831462 | CGCACTGCTCACAGC[A/G]ATTTAGTGCTGGGTG | 257397 |
rs749583003 | in-del | -/ATATATA | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30839918 | ACATATATATATTAT[-/ATATATA]TATATATATATATAT | 257397 |
rs749590336 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30833329 | AAAAGAACAATATGC[C/T]CAAAAACGTAACACT | 257397 |
rs749601397 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889825 | AACCCTTTGCTTGTC[C/G]TTATGGGTTTTGTCA | 257397 |
rs749615650 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30859835 | CCTCTCCCCTCCACA[A/G]TGCTGCCAAAGCAGG | 257397 |
rs749616607 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30880915 | AAACTGTAAAATAAT[G/T]ACTCCTGAAAAGTCC | 257397 |
rs749669178 | snp | A/T | 5.28011e-05 | 0.00513788 | intron-variant, stop-gained, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846045 | GGGTAAATGAAAGTT[A/T]AAGAGAGCTTCTGCT | 257397 |
rs749673941 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30882813 | GTCTCACTAACAATA[A/G]TGTACCAATGTTAAT | 257397 |
rs749676902 | snp | C/G | 3.19096e-05 | 0.00399422 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859595 | TTGCGCCATGCCAGA[C/G]CAAATGGTGGCCAAG | 257397 |
rs749689686 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30874579 | ATTCACAGGCCTAAC[A/G]TAAAATAATTGTTCA | 257397 |
rs749759029 | snp | C/G | 2.31887e-05 | 0.00340497 | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846628 | TTCATGCTTCTCAAT[C/G]TTGTCATTTCCTCAG | 257397 |
rs749805432 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30855691 | CAGTATTTTAACCAC[-/A]AAAAAACTTCATGGT | 257397 |
rs749826158 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30879221 | TCACTGCTAAAATCT[A/G]TCATGCATTTAAAGA | 257397 |
rs749839445 | snp | A/G | 0.00528398 | 0.051128 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890412 | TGCGACTACAGGTGT[A/G]TGCCACCATGCCCGG | 257397 |
rs749843951 | snp | A/C | 2.29679e-05 | 0.00338872 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852859 | ATTAACTTCAGACTT[A/C]AACCGCTCTAGCTCC | 257397 |
rs749860335 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30861808 | TAGGTGAAATTAATT[C/G]TAACATTTAACCCAT | 257397 |
rs749874745 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833798 | ATAGCGCCACTGCAC[C/T]CCAGCCTGGCCTAAA | 257397 |
rs749922613 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30857161 | AACATTCTACCCAGA[A/T]GATAGTGACAAATGG | 257397 |
rs749926220 | in-del | -/TAAGG | 0.000103545 | 0.00719457 | intron-variant | TAB3 | GRCh38.p7 | X:30831593 | GAGGGAGGTTAGGAT[-/TAAGG]GGGAGGGGGAAGGTA | 257397 |
rs749926327 | snp | A/T | 2.51203e-05 | 0.00354394 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855010 | AGAGATTGCTTGGAA[A/T]TTGTGGAAGAATTTG | 257397 |
rs749937601 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30868847 | TACAACCACAGTAGA[A/G]CTAAAATAACATACC | 257397 |
rs749938917 | in-del | -/GCC | 0.0115254 | 0.0750325 | utr-variant-5-prime, cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30889257 | CGGGATCCGGTGTGA[-/GCC]GCCGCCGCCGCCGCC | 257397 |
rs750018470 | snp | C/T | 9.13138e-05 | 0.00675637 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855158 | CCCTTGCATAGCAGA[C/T]GGATTCATTCCTGTT | 257397 |
rs750041533 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828985 | TGCCTATTTTAAAAC[C/T]GAATACAGCCTATGT | 257397 |
rs750042083 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859849 | AATGCTGCCAAAGCA[A/G]GCTGTGCTTACCCTC | 257397 |
rs750055781 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30827912 | TACTGTTAATTCTTT[C/T]GAAAAGATACAGTAG | 257397 |
rs750102674 | snp | A/C/G | 7.08037e-05 | 0.00594959 | missense, stop-gained, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834117 | TCACGCTAATTCTTC[A/C/G]GGCTTTTCTCTCAAT | 257397 |
rs750104908 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869485 | TTTCAGCACTTAGTA[C/T]ATTAACTTTTTATTC | 257397 |
rs750177452 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30865120 | GTGTCTCAACGGCAT[A/G]CTATTGATGCAATAA | 257397 |
rs750197834 | snp | A/G | 2.29822e-05 | 0.00338977 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852785 | TCACTTACCGTAGGG[A/G]TCGCAGTGGTGCAGC | 257397 |
rs750212743 | snp | A/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846225 | TATTTTAGATGTCTA[A/T]CACATAATATGAACT | 257397 |
rs750212999 | in-del | -/AA | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863881 | TAATCCAATAGAAAC[-/AA]AATGAAAACACTGTC | 257397 |
rs750234693 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30872437 | ACTGTTCGCTCAGGA[A/T]TGGAAGACCTTCCCC | 257397 |
rs750262028 | snp | A/C | | | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827296 | AATGTGCACTTAATA[A/C]CCCAAATCTAACATT | 257397 |
rs750262632 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841138 | TTTAGAAATCAATAG[A/G]CTATTTTTTGGCCAG | 257397 |
rs750376302 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853123 | CTGAATGCAACCAAA[A/G]TGACATCACCTGAAC | 257397 |
rs750392026 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888181 | TTCAAAATGAAAAAG[C/T]GCGCAAAGAAAGCTC | 257397 |
rs750406873 | snp | C/G | 2.56944e-05 | 0.00358421 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854893 | GGCTATAGTGAGGCA[C/G]TGGGCCCTGTGGTGA | 257397 |
rs750424142 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832715 | ATGCTCAGCCTCAAA[C/T]AGGAAGGTGATCTTA | 257397 |
rs750443618 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30882355 | AGAAGTATGCTTAAC[A/C]CTTTTTTAATAGGAA | 257397 |
rs750509457 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30867228 | GAATCCTGAAAGAGG[-/A]AAAAAAAACATGTTC | 257397 |
rs750597225 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863490 | GAGGTGACTGGATGA[C/T]AGGGGCAGAGCCCTT | 257397 |
rs750632272 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30857941 | TTCCTAAAAAGTGAT[C/G]CTAAATTGAGGATGA | 257397 |
rs750634424 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848351 | CAACATGGCAAAACC[A/G]TCTCTATTTAAAATA | 257397 |
rs750685902 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834455 | GTACAAACTCAGTGA[C/T]AGCAAATAAATGTCG | 257397 |
rs750753554 | snp | A/C | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891283 | AGCATGGCACTGAGA[A/C]TTTTCCTTATTACGT | 257397 |
rs750766089 | in-del | -/TATATAGCT | | | intron-variant | TAB3 | GRCh38.p7 | X:30868308 | GAAAAGCTATATATA[-/TATATAGCT]TATATATATATATAT | 257397 |
rs750806515 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30872723 | CTAATTCATGCACCA[A/G]TAATCAATGGATGCT | 257397 |
rs750819577 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30851501 | TGTTTAAGGCAATGG[G/T]TCCTCACTCCTTTTT | 257397 |
rs750824213 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30853280 | TATCTTGAAACAATC[C/T]GAATAGACTTTTTAA | 257397 |
rs750828060 | snp | A/T | 3.07059e-05 | 0.00391817 | intron-variant | TAB3 | GRCh38.p7 | X:30854096 | CAGAAATTAAATTTC[A/T]TAAAAGGGTTAAAAT | 257397 |
rs750866170 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842741 | TGAGGCAGAAAGATC[A/G]CTGGAGCCCAGAAGG | 257397 |
rs750955776 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30885808 | TCATCCTCCTTTTCA[A/G]GAAAGAACAGGGTGG | 257397 |
rs750986236 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30841997 | TATTTTTAGTAGAGA[C/T]GGGGTTTTGCCATGT | 257397 |
rs751002143 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852995 | AACAAGCGACTGGAA[A/G]ATTTCGATATGCACT | 257397 |
rs751029228 | snp | A/C | 4.78899e-05 | 0.00489312 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834130 | TCGGGCTTTTCTCTC[A/C]ATTGTGCAGGGGTCT | 257397 |
rs751058999 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874101 | CACTTGAGCCCAGGG[G/T]ATTGAGGCTGCAGTG | 257397 |
rs751061920 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832374 | CTAGAGTTAACCTGT[A/C]ATTTCTGTCTTTTAG | 257397 |
rs751063732 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30875303 | TAACCTCTTAGGCCC[A/C]GTTTCCTAATCCTTT | 257397 |
rs751077363 | snp | C/T | | | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30826961 | GACCTCCCAAAGTGT[C/T]GGGATTACAAGCATA | 257397 |
rs751104917 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888009 | TGTTCATAAAACACA[C/T]CATCACAAAACTTAC | 257397 |
rs751105137 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876271 | TTCTGAAAAACTATC[A/G]TCCTTGGTTTCAAAT | 257397 |
rs751159258 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846252 | AACTCTACTAAGTTT[C/T]AGAATTAAAACCCAT | 257397 |
rs751167641 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30877017 | AATGATGAAACCTGT[C/G]AAACCACATGTGTAA | 257397 |
rs751169321 | snp | C/T | 3.19811e-05 | 0.00399869 | synonymous-codon, intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30842976 | CTCACCTTTTTTAGA[C/T]GGCTTGGGTGGTACA | 257397 |
rs751193094 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30835956 | TATCTTTTTTCTTTT[G/T]GTATTTGAGTGGCCT | 257397 |
rs751290798 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30839791 | CAAAGAGTTTAAGAT[C/T]GGTATTTTTACTTTC | 257397 |
rs751322256 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883959 | TATTTTAATAAAGAC[A/G]TTGCAATTACTCAAA | 257397 |
rs751333635 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844690 | AGTTAGTGGGCTATA[A/G]AGTGACTAGGCTTCT | 257397 |
rs751353031 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30871468 | GCAAATGAATTGTCC[A/G]AAGAACTTGTAACTC | 257397 |
rs751362328 | snp | G/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30881358 | AGTAAGAGGTTTTTT[G/T]TTTTTTTTTTAAGTG | 257397 |
rs751374383 | in-del | -/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843680 | TTTATCAATGATAAA[-/T]AGGTGCCAATTTCAG | 257397 |
rs751377301 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863327 | ACTTTAAAAAAGCAA[C/T]TTCCATTTTGTTCAC | 257397 |
rs751379001 | in-del | -/TGA | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848840 | AGCGTCAAAGACCAC[-/TGA]TGATGTTCTTTGGTG | 257397 |
rs751445495 | snp | C/G | 2.33997e-05 | 0.00342043 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855036 | ATTTGTAAAGCTCTT[C/G]GTACAGTCTGTCCAG | 257397 |
rs751445710 | snp | C/G | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845863 | TAACTGGCATAAACA[C/G]GTTTGGGGACAGAAT | 257397 |
rs751448978 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30863738 | CCTGAGCCAATTAAA[C/T]CTCTTTTCTTTATAA | 257397 |
rs751459870 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831849 | TTACCTGTAAATAGC[A/G]GAGAGTTATGCTTTA | 257397 |
rs751474031 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852368 | TGATCTAACTCATCT[G/T]AATTAATGTACTTAC | 257397 |
rs751500289 | in-del | -/TTTG | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30872375 | CTTTTCTTCTGTTTT[-/TTTG]TTTGTTTTTCCCTGC | 257397 |
rs751503044 | snp | C/T | 2.28165e-05 | 0.00337753 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855188 | TTGCATGGAAGATGG[C/T]TGTTGAGGTGGTTGT | 257397 |
rs751658602 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30874376 | TTAAATTATTGGGGA[C/G]TGAAATTATGTCTTG | 257397 |
rs751665169 | snp | C/T | 2.67115e-05 | 0.00365446 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859557 | AGATCATGGAGAACC[C/T]GAATATCAAGCTGTG | 257397 |
rs751688347 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30865149 | AATTTTGGAGCACAA[A/G]AATTCCTCGTCATGC | 257397 |
rs751792686 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30867157 | TCTGAGAAACTGTCA[C/T]AGCCAAGAGGAGTCT | 257397 |
rs751794247 | snp | A/C/G | 6.84205e-05 | 0.00584855 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855262 | ATGGATTGTAGTTGG[A/C/G]AGTAGCAGCAACAAC | 257397 |
rs751803041 | snp | C/G | 0.0026455 | 0.0362733 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889517 | ATAAGTTAGGGAAGC[C/G]TGAGCAAACGCTTCC | 257397 |
rs751839966 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30881820 | TCTAAACAATTCAAG[C/T]TATTTAATTAAGTTC | 257397 |
rs751841047 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869463 | GTCACTGTGTGTTGA[G/T]TATCACTTTCAGCAC | 257397 |
rs751848186 | in-del | -/T | 0.00105904 | 0.0229869 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842668 | AAAAAATAAAAAAAA[-/T]ATTAGCTGGGCATGG | 257397 |
rs751879061 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30833249 | GCTGGGATTACAGGT[G/T]TGAGCCACCGCACCC | 257397 |
rs751928207 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30888391 | ATTTCAGTAGAAACA[A/G]AAGGATTTACACTTT | 257397 |
rs751951786 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30871076 | GAACATTTTCATAAG[A/G]TAGAAAGATAAACTA | 257397 |
rs751965433 | snp | A/G | 2.28243e-05 | 0.00337811 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854277 | AAAAGATTTTCAGTC[A/G]TTGCTCGGCCTACGG | 257397 |
rs751998403 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30836895 | AGGTACTTGTAGAGC[A/G]CTAGATGAAGCTTGA | 257397 |
rs752008588 | in-del | -/CAG | | | intron-variant, cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836632 | AGGATCGCTTCAGCC[-/CAG]GAGTTTGAGACCAGC | 257397 |
rs752039730 | snp | C/T | 0.00317376 | 0.039709 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883906 | GAAATTGAGGCTCCC[C/T]CTGCACAGACTCTAG | 257397 |
rs752055406 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30849893 | TTTATGTGTCTAAAC[C/T]TCAAGCAAAGTTGTC | 257397 |
rs752064497 | snp | A/T | 0.0845627 | 0.187431 | intron-variant | TAB3 | GRCh38.p7 | X:30859685 | AGTCATTTTCTATTT[A/T]AAAAAAAAAAAAAAG | 257397 |
rs752089026 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30886297 | TTCAGAAAGGCTTTA[A/T]TTACTTGGTAAGCAT | 257397 |
rs752100495 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830014 | AATTCTGAGCTAAGA[A/C]GGAACTCCAACAATG | 257397 |
rs752118373 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850101 | TACATGAGTGACAAA[C/T]AGAAGTAGGATTCAA | 257397 |
rs752119733 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862487 | GAAGAATCAAAACAC[A/G]GACAGACAGGCTTCA | 257397 |
rs752154475 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891392 | CATTCCTAGACTGTC[A/G]TCCTAGTCTACATGG | 257397 |
rs752172647 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30840460 | ATTTCCTGAGTAACG[A/G]CAGTGTCTTTGTTAT | 257397 |
rs752199168 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845579 | TGGCTATCGCTCCAC[C/T]AAAACTTTTATTCAC | 257397 |
rs752228195 | snp | C/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890353 | CACTCCAACCTCAGC[C/G]TCCCAGGTTCAAGTG | 257397 |
rs752232804 | in-del | -/C | 0.0806904 | 0.183941 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830913 | CCCTTAATTAATTTG[-/C]CCCCCCCCCCCAAAT | 257397 |
rs752248935 | snp | C/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844395 | TTCTGAAAATAATTG[C/G]TGTGATAGCTCATAA | 257397 |
rs752271515 | in-del | -/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30871428 | TGCTAAATTACCCTT[-/C]TATTTTCTGGTGAGG | 257397 |
rs752321807 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875279 | GTGTGGGACGACAGA[C/T]GAGTTACTTAACCTC | 257397 |
rs752322974 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30861375 | TCCTGCCATCCCCCC[-/A]ACCCAGCAAATGTCA | 257397 |
rs752390370 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831785 | AATTACTTTTTTTCT[A/G]CTATAAGAAGATGGA | 257397 |
rs752394284 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30875709 | GTCCATTGTCAAGGT[C/G]TAGCAATTGACCAAG | 257397 |
rs752409977 | snp | A/G | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30847329 | TTCCATTTGTTCCCC[A/G]ACTTTGTTTTCTTCT | 257397 |
rs752429946 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30832026 | TGTGCCTTCTTCCAT[A/G]ACAACTTAAGCTCTA | 257397 |
rs752525066 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30881670 | TTTTGTTAAACAAGA[G/T]GGTTTTTACATCTTA | 257397 |
rs752527673 | snp | C/G | 4.56048e-05 | 0.00477497 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855211 | GTGGTTGTGAAGGAG[C/G]AGTAGCTGCACTTCT | 257397 |
rs752529438 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890179 | AAACAATGACGACAC[C/T]TTAGCACAGTAAGTT | 257397 |
rs752586520 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871334 | TTATTTCTTGGGGGC[A/C]GATCTTTCAATCTCC | 257397 |
rs752599609 | snp | C/T | 3.3394e-05 | 0.00408606 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843034 | AAATTATTCATGGCT[C/T]TTGGATCAAAGTTTC | 257397 |
rs752619684 | snp | C/T | 9.50819e-05 | 0.00689434 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855470 | GCGATTTCTATTCAT[C/T]CTATTGTCATCTGGA | 257397 |
rs752634877 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30861503 | CCTTTTGAAAACTCC[A/G]AATCTGAAATACTAA | 257397 |
rs752635805 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30881220 | AGGGATGGGGGTGGA[-/G]GGGGGGTAAGGTAGT | 257397 |
rs752642899 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838612 | CTATATATCAACCTT[G/T]TAAGAACAGGTATCT | 257397 |
rs752796556 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30849967 | TTTGTTGGGCATTGT[A/G]TAAACTGCTTCACAT | 257397 |
rs752809938 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883727 | TGTACTCAGTGCATG[C/T]TCCTGCTGAGACACT | 257397 |
rs752816601 | in-del | -/CAAA | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30864986 | CTCCGTAGCTGATTC[-/CAAA]CAAACACTGCAGCCT | 257397 |
rs752848527 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30849464 | GTTTGAAAACTTGAA[C/G]GTAGCAATGTGTGCT | 257397 |
rs752852470 | snp | A/G | 6.8865e-05 | 0.00586752 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852788 | CTTACCGTAGGGATC[A/G]CAGTGGTGCAGCTGA | 257397 |
rs752864887 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30882736 | CAACTCAGTGCAACA[C/T]GGTATCCTGGAACAG | 257397 |
rs752899954 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30851193 | AATATTGACTATACA[C/T]GATATTACAAAAAAG | 257397 |
rs752904865 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830364 | TAAGTTTTTATTGAA[C/T]AGTTAATATTGATTT | 257397 |
rs752908175 | snp | C/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30832896 | GTAGATTTAATACAG[C/T]TTTCTTTTTTGTCTC | 257397 |
rs752942327 | snp | C/T | 2.56621e-05 | 0.00358195 | intron-variant | TAB3 | GRCh38.p7 | X:30852978 | TGCAGAGAACAACAT[C/T]GAACAAGCGACTGGA | 257397 |
rs753000250 | snp | C/T | 2.32842e-05 | 0.00341198 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854742 | GGTTGCACTTGATGC[C/T]GTGGAGAGCTGAAGG | 257397 |
rs753025554 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841291 | CCGGGCATGGTGGTG[A/G]GTAATCCCAGCTACT | 257397 |
rs753046320 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30837816 | AACTTTTATACTTAG[A/G]TGTATGAGCTATCTC | 257397 |
rs753058546 | in-del | -/GCT | 0.00844758 | 0.0644393 | intron-variant | TAB3 | GRCh38.p7 | X:30868385 | GCTTATATATATATA[-/GCT]TATATATATATATAT | 257397 |
rs753101447 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30840136 | TTCACTTTTGATTGT[A/G]GTAATTTGTGTTCTC | 257397 |
rs753111197 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886587 | GAAGACAGGACTACT[A/T]AACTGAAGGCCCCCA | 257397 |
rs753127140 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827241 | AACTTTTATGTAAAA[C/T]CTGCTTATGTATAAT | 257397 |
rs753134734 | snp | G/T | 0.00475684 | 0.0485365 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844798 | TGCCGTGTCTTTTGG[G/T]TTCACCTGCCACTAA | 257397 |
rs753156428 | snp | A/C/T | 0.00105918 | 0.022993 | intron-variant | TAB3 | GRCh38.p7 | X:30876245 | ATGTACACACACACA[A/C/T]ATACACTCCTTTCTG | 257397 |
rs753205063 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888326 | TCGAACTGACAAGCC[C/T]GGTCTGGACCAAAGG | 257397 |
rs753220100 | snp | C/G | 0.00481667 | 0.0488378 | intron-variant | TAB3 | GRCh38.p7 | X:30868636 | CGTGGGGGGGAGAGA[C/G]AGAGAGAGAGAGAAT | 257397 |
rs753220111 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858323 | TCCTTATTTGGTTTC[A/T]CTCCGGTGGGAAGTG | 257397 |
rs753280584 | in-del | -/TAAT | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30870503 | TGGGGTTGAGTTCTA[-/TAAT]TAATAAGTAGTCAGA | 257397 |
rs753294054 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835733 | GTATTGCTTAACTAC[A/G]AAGTCCAATCCAAAA | 257397 |
rs753318219 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30866070 | GAGACCATTTTGAAA[C/T]AGTCACATATTCACT | 257397 |
rs753362184 | in-del | -/T | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30850706 | GACAGGGTGAGACTC[-/T]CCATCTCAAAAAAAA | 257397 |
rs753365683 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838374 | GCCCAGGCTAGTCTC[A/G]AACTCCTGAGCTCAA | 257397 |
rs753388340 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30833368 | AATTCGTATCTTACT[A/G]TTGCTGGTTTTTAAT | 257397 |
rs753434159 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869826 | TAATGTATTGTATAA[C/T]AAATGTACTACGTGA | 257397 |
rs753452244 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885237 | TTTTTAAAATCATCT[A/G]TTTGAAACTCAGACT | 257397 |
rs753472812 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830178 | CCTGTAGAGACTCAA[C/T]TGACCTCTAGATACA | 257397 |
rs753477840 | snp | A/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844034 | ACAAAAAAGCTGGTT[A/T]TCATCAAGTCATGCA | 257397 |
rs753504478 | snp | A/C | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30862406 | TCATTTTCCAACCTT[A/C]ATTACAAGCCTTTAA | 257397 |
rs753506158 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30851582 | TTCCCATATTAAACA[A/C]ACTTATGAAACTCTG | 257397 |
rs753523179 | in-del | -/CACAAACT | 3.29473e-05 | 0.00405864 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834022 | TCTTTGGACATTCTG[-/CACAAACT]CACAAACTCTGGACA | 257397 |
rs753525184 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30839410 | AATGAGATAGAAAAC[A/G]GAATTATGGATTTTT | 257397 |
rs753545744 | snp | A/C | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890165 | AGATGAATGAGAAAA[A/C]ACAATGACGACACTT | 257397 |
rs753550203 | in-del | -/TTTG | 0.01368 | 0.0815649 | intron-variant | TAB3 | GRCh38.p7 | X:30853678 | ACTAACTTTATTCTT[-/TTTG]TTTGTTTGTTTTGGA | 257397 |
rs753552750 | snp | C/G | 6.45619e-05 | 0.00568127 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831392 | CTGGTAGTGCTCAAA[C/G]TTTCACTTTCAACCT | 257397 |
rs753570796 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30889384 | GCTCTGGCTTCAGGG[C/T]TTCCGTCGGGCGCCG | 257397 |
rs753573431 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30849281 | AATGACACCATCATG[A/C]ATCTTATATCTTGCA | 257397 |
rs753603831 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30877324 | AACCCTCACTAAGAA[C/T]GAAGCAAAAGAAAAC | 257397 |
rs753613461 | snp | G/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829231 | TGCAATAGTTTTAAA[G/T]TCATCTACATGGTTT | 257397 |
rs753639789 | in-del | -/GTAA | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30866104 | TCTATCTCATATTCT[-/GTAA]GTCTCAAGAGATATA | 257397 |
rs753660946 | snp | C/T | 5.21227e-05 | 0.00510477 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859510 | TGCACTGAGACACCA[C/T]GCCCTCTGGAATTTC | 257397 |
rs753671694 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830177 | GCCTGTAGAGACTCA[A/G]TTGACCTCTAGATAC | 257397 |
rs753768964 | snp | A/C | 2.79291e-05 | 0.00373681 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846514 | GCTTAAAATACCACA[A/C]TATTACTTATGGTTT | 257397 |
rs753802968 | snp | C/T | 0.00105904 | 0.0229869 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890083 | TTCAAACGTGTGTTG[C/T]TCAGTTTCCTATGTG | 257397 |
rs753860617 | snp | A/G | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833969 | AAGCAAAAAATAAAG[A/G]TATGGTTTTACTTAT | 257397 |
rs753919716 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858108 | AGGAAGAAAAAAGTG[-/A]AAAGACTTAGGACAG | 257397 |
rs753985760 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30865432 | TTGAACAAAACACAG[G/T]ATGTATATGAGTATA | 257397 |
rs754004039 | snp | A/T | 4.5647e-05 | 0.00477718 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854222 | AATGGGCTGAATAGG[A/T]TCTGGTGCTGCAGAG | 257397 |
rs754037484 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30848245 | ATACTTTCATCAGGC[C/T]GGGTGCAGTGGCTCA | 257397 |
rs754050471 | in-del | -/AGAC | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840878 | CCAATGCACTCCCTT[-/AGAC]AGGGCAATTGCTCTA | 257397 |
rs754106434 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30826983 | ACAAGCATAAGCCAC[C/T]GTGCCCAGCCTGGAA | 257397 |
rs754119519 | snp | A/C | 4.8886e-05 | 0.00494375 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831547 | TCGAGGTTGTGTCCG[A/C]GGACTTTGTGTGGAG | 257397 |
rs754151672 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848890 | TCTGGGACTCAAAGC[G/T]GTGGGATAGTCCAAA | 257397 |
rs754175528 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30853423 | ACTTCTTATATATTA[C/T]TTATATGTAAATATC | 257397 |
rs754175566 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30875047 | AATGGGGTGGGAGGC[A/G]GTGAGGATGAGATAT | 257397 |
rs754188040 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875163 | ATAATATGATAAAAC[A/T]GGGAAGTCAGTGAGC | 257397 |
rs754211083 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842850 | AAAATAATAAAAATA[C/T]GGTAACTTTATGCTG | 257397 |
rs754218672 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878228 | GGGTGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC | 257397 |
rs754226896 | snp | A/G | | | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854879 | AGGTAAAGGACGCTG[A/G]CTATAGTGAGGCACT | 257397 |
rs754228425 | in-del | -/AT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852179 | GGATCGTTAGAACTC[-/AT]ATATATTAACCAACA | 257397 |
rs754238135 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30837197 | AGGATTACAGGTCCA[C/T]GCCACCATGCCCAGC | 257397 |
rs754239956 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834707 | CTCACTGCAGCCTTG[A/C]TCTCCTGGGCTCAAG | 257397 |
rs754248225 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30857177 | GATAGTGACAAATGG[C/T]AATTATAATCAATAT | 257397 |
rs754257969 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835469 | GCTGGATTGTCCCTC[C/T]ATGGTGCTCAGATTG | 257397 |
rs754286887 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30886395 | TACTTTCACAAGTAA[-/G]GAAGTATATTTTATT | 257397 |
rs754366995 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843803 | TTCAGCCACATCTCC[C/T]GCTGTGTCTCCTCCA | 257397 |
rs754427130 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888533 | ACTACAGAACTCCAA[C/T]TGGGAATAACTCTAA | 257397 |
rs754453131 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884779 | TATGTAACCTCAACA[C/T]GCTAACACTTTATTT | 257397 |
rs754473895 | in-del | -/C | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30850858 | AAAAACAAAAAAAAA[-/C]CAATATTTTATTTAG | 257397 |
rs754475505 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30861375 | CTCCTGCCATCCCCC[A/C]ACCCAGCAAATGTCA | 257397 |
rs754480123 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830191 | AATTGACCTCTAGAT[A/G]CAGTTATGTTAAATT | 257397 |
rs754485676 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30842029 | GGCCAGGCTAGTCTC[A/G]AACTCCTGGCCTCAT | 257397 |
rs754527772 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838455 | CATTGCACTGAGCCA[G/T]TCTAAGACTTCTGGA | 257397 |
rs754531479 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30857805 | GTCTTTAAAGAAAAA[-/T]AAGGATAAAAAATGT | 257397 |
rs754576564 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870530 | CAGAAAAAGAAACAA[C/T]GAAGGTAGAACAAAG | 257397 |
rs754581256 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30886106 | TTATTTAGGATTAAT[G/T]CAGTTTGATAGTTCC | 257397 |
rs754617667 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30869509 | TTTATTCTCCTCTAG[A/G]ATTTTTCACTATAAA | 257397 |
rs754671070 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30871312 | CGTATATCCCACACA[A/C]ATCTAGTTATTTCTT | 257397 |
rs754679425 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30878716 | GCTAAGCCATAAAGT[A/C]AGTCTCAGGGCATTT | 257397 |
rs754705740 | snp | A/G | 4.60056e-05 | 0.0047959 | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846592 | TTCAGTGTACAGTCA[A/G]CATTTATCTGGAGTT | 257397 |
rs754721792 | in-del | -/AGAA | 2.87753e-05 | 0.003793 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834175 | AAAATAAACAACGCC[-/AGAA]AGAAGTGATCCAGTC | 257397 |
rs754733085 | snp | C/T | 6.84939e-05 | 0.00585169 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854283 | TTTTCAGTCGTTGCT[C/T]GGCCTACGGTAATTT | 257397 |
rs754757511 | snp | G/T | 2.3179e-05 | 0.00340426 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855042 | AAAGCTCTTGGTACA[G/T]TCTGTCCAGAAGGGA | 257397 |
rs754760183 | snp | A/C | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830226 | AAGTTGTTTCAAAGT[A/C]CTCTATATTCACCTT | 257397 |
rs754771196 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-5-prime, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889394 | CAGGGCTTCCGTCGG[A/G]CGCCGTCGCTCGCCA | 257397 |
rs754805452 | in-del | -/A | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30877837 | TTATCAGATTGGGTT[-/A]AAAAAAATCTACAAC | 257397 |
rs754836984 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869847 | TACTACGTGATGACT[A/G]TAAGGGGAAAAGAAA | 257397 |
rs754845352 | snp | A/G | 2.67745e-05 | 0.00365876 | intron-variant | TAB3 | GRCh38.p7 | X:30831603 | AGGATTAAGGGGGAG[A/G]GGGAAGGTAAATAGA | 257397 |
rs754869753 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30879148 | ACTATTAGTATTTTT[A/T]AAACTGCATCTGTAA | 257397 |
rs754935832 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30837345 | AGCATGAGCCACAAG[C/G]CTGGCCTCAGAATGA | 257397 |
rs754948996 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30857416 | TGAAGGAAAAAAATA[C/T]GGAAGGTGAAATAAA | 257397 |
rs754978969 | snp | C/T | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827041 | CACTGAAAATGTTAC[C/T]TACTATAATTCATTT | 257397 |
rs754992859 | snp | C/T | 2.44879e-05 | 0.00349905 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855520 | AGTATTTGCTACTCT[C/T]CTGGGAAAGGGCTCG | 257397 |
rs755002725 | snp | A/C | 2.5214e-05 | 0.00355054 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834147 | TTGTGCAGGGGTCTG[A/C]GGAGTCTGCATAAAA | 257397 |
rs755018465 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30840931 | TGAACTAAAGTTTGT[A/C]TGGCGATACTTCTTT | 257397 |
rs755023062 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30846859 | ACATATAAACAAAAT[A/C]TGCATATAAAGTGGC | 257397 |
rs755059170 | in-del | -/AC | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30882446 | TTTAGTCCCATGAAA[-/AC]ACAGTTTTAAATTAT | 257397 |
rs755108522 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30881574 | ACTATTTGAACCCAA[C/T]TGATAAACTGACTTA | 257397 |
rs755122305 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862801 | CCACTGTGTCACTAG[C/T]AGGTATCAGAGACAT | 257397 |
rs755155721 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30848492 | GCACCACTGCACTCC[A/G]GCCTGAGCAACAGAG | 257397 |
rs755192598 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30872528 | AATCACTTTATCATA[A/G]GCCTTAGTAAAATAA | 257397 |
rs755201012 | snp | C/G | 2.35752e-05 | 0.00343322 | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846553 | ATCAAGTCTATACCT[C/G]TAGATTGAAGGAGGT | 257397 |
rs755201783 | snp | A/C | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829273 | AGACTGTTTTCAGAC[A/C]TGCTACTTTCATTCT | 257397 |
rs755270353 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30849365 | CCTCCCTCCCCCACA[C/T]AGCTGGTCACAAATG | 257397 |
rs755284942 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835494 | AGATTGAGTTTGAAC[A/G]AGGTCAGGTGGCCAA | 257397 |
rs755285905 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840891 | TTAGACAGGGCAATT[C/G]CTCTAAGACAGCTCT | 257397 |
rs755334746 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842922 | AAATCCCAAATTATT[C/T]TGACATTTATTTCTA | 257397 |
rs755338283 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30837238 | ATCTTTAGTAGACAC[A/G]GAGTTTCACCCTGTT | 257397 |
rs755352170 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843807 | GCCACATCTCCTGCT[A/G]TGTCTCCTCCAAGGT | 257397 |
rs755452674 | in-del | -/ATA | 0.306731 | 0.243478 | intron-variant | TAB3 | GRCh38.p7 | X:30868368 | TATATATATATATAT[-/ATA]AGCTTATATATATAT | 257397 |
rs755512528 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834709 | CACTGCAGCCTTGAT[A/C]TCCTGGGCTCAAGTG | 257397 |
rs755526108 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891345 | CCACAAAGTGAGCCA[C/T]GGTTTAGTCTCCCTA | 257397 |
rs755567336 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863860 | ATTATGCTGTACTTT[C/T]GTATTTAATCCAATA | 257397 |
rs755638989 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30837090 | ATCTTGCTCTGTCAC[C/T]CACGTTGGAGTGCAG | 257397 |
rs755643893 | in-del | -/CACACACACACACACA | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859361 | AGGGAAATCCTGCTC[-/CACACACACACACACA]CACACACACACACAC | 257397 |
rs755664968 | in-del | -/G | 0.00105904 | 0.0229869 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846413 | CATGACCATGGGACA[-/G]GGGGGATCTCTTTCC | 257397 |
rs755672069 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830108 | TTTATATCTCTTATC[C/T]GCACCCTGAAGTTCT | 257397 |
rs755673179 | in-del | -/G | 7.98509e-05 | 0.00631816 | intron-variant | TAB3 | GRCh38.p7 | X:30831602 | TAGGATTAAGGGGGA[-/G]GGGGAAGGTAAATAG | 257397 |
rs755675535 | snp | A/C | 2.28477e-05 | 0.00337984 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854305 | CGGTAATTTTAAAAA[A/C]TGTAGTTGGGTTTGG | 257397 |
rs755697088 | in-del | -/AAA | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30868942 | TTACTTTGATTATCC[-/AAA]AAAAAAAAAACTAAC | 257397 |
rs755724906 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30838332 | TGGCTAATTTTTAAA[-/T]TTTTTTTTGTAGATG | 257397 |
rs755783201 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30888467 | CCTCACCTGTCCCTC[A/G]CCCTTCAAATCCTGC | 257397 |
rs755796498 | in-del | -/GTTT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30864953 | CTTTTAGGAAGGACA[-/GTTT]GTTTGCCTAGTTCCT | 257397 |
rs755805171 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30859876 | CCTCACAGAAACACT[A/G]AACACGCTATACTGA | 257397 |
rs755842136 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853143 | ATCACCTGAACATCC[C/G]TCTTGTTCTATTGTC | 257397 |
rs755851209 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848183 | GTTTCAGCCACAGTG[A/G]CCCAAAACAGTGAAG | 257397 |
rs755858238 | snp | C/T | 2.37516e-05 | 0.00344604 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854814 | TGAGGGATCTGCTGC[C/T]GTTTGGGAGAATACT | 257397 |
rs755865754 | snp | C/T | | | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827422 | TACTGTAAATTTCTA[C/T]GCAGAAAAGATGCAG | 257397 |
rs755918500 | snp | C/T | 2.28042e-05 | 0.00337663 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855214 | GTTGTGAAGGAGGAG[C/T]AGCTGCACTTCTGTT | 257397 |
rs755920696 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829221 | TGTATTTTCATGCAA[C/T]AGTTTTAAAGTCATC | 257397 |
rs755943633 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831142 | TGGGATTCCACCACA[A/G]AAGAGCTCTTGACTT | 257397 |
rs755967252 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832738 | TGATCTTAGCCTTAG[C/G]ATATAACAGAAAATT | 257397 |
rs755992654 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30864102 | AGGACTCAAGCAGTA[A/T]CTAAGCTGTACAGGC | 257397 |
rs756018623 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841231 | TTCAAGACCAGCCTC[A/G]CCACCATGGTGAAAC | 257397 |
rs756050841 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30888226 | TTCCCTTTTCTCATT[A/C]ATTCTTGTTCTTTTA | 257397 |
rs756064074 | in-del | -/T | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30853656 | GTCTATACATGACTC[-/T]TGAAGCACTAACTTT | 257397 |
rs756066294 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30860961 | CAGTTCAGAAAAAAA[-/T]ATATGTACATGTGTA | 257397 |
rs756072015 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845174 | GAGATATTTTATTAT[A/G]TACTCTTAAAACACT | 257397 |
rs756080143 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30856983 | CTGGAGCTTTAGGAA[A/G]TTTAAAAAAAAGTCC | 257397 |
rs756101015 | snp | A/C | 0.000190288 | 0.00975231 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843056 | CAAAGTTTCCTATAA[A/C]GAAAGTAAATTCATC | 257397 |
rs756115468 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30875774 | GAAACAATTTACTTA[C/T]ATTTACGCACATACA | 257397 |
rs756131405 | snp | C/T | 2.30274e-05 | 0.00339311 | synonymous-codon, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846582 | GTCAACTTCTTTCAG[C/T]GTACAGTCAACATTT | 257397 |
rs756150928 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30861724 | AGCTCTAAGGCAGCA[A/T]TGTCCAGTAAAAAAT | 257397 |
rs756164632 | in-del | -/CAC | | | intron-variant | TAB3 | GRCh38.p7 | X:30855922 | GGCTTATCTCGGATT[-/CAC]CACAATTGCTGCAAT | 257397 |
rs756168445 | snp | C/G | | | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855496 | CTGGACTATGGTATT[C/G]CATATATAAGTATTT | 257397 |
rs756173430 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891242 | CCAACTCACAAACCC[A/G]TGAGTGAGAAATAAA | 257397 |
rs756206274 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867229 | GAATCCTGAAAGAGG[A/G]AAAAAAACATGTTCA | 257397 |
rs756221279 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852831 | GTCTCTGCATCAGGT[C/T]ATGCTCCATACCATT | 257397 |
rs756235738 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833724 | TAGTCCCAGCTACAC[A/G]GGAGGCTGAGGCAGG | 257397 |
rs756275282 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30855652 | AGAGTTATGCAAATA[C/T]TACTGTCACAGAATA | 257397 |
rs756298959 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870833 | CAGGACAGCCCCTGA[C/G]AACAGAAAATTATCC | 257397 |
rs756366281 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846445 | AGGATTGTAATCTTA[C/T]GGATAAAAACTGTCT | 257397 |
rs756376217 | snp | A/G | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30842001 | TTTAGTAGAGACGGG[A/G]TTTTGCCATGTTGGC | 257397 |
rs756390305 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30851579 | CACTTCCCATATTAA[A/G]CACACTTATGAAACT | 257397 |
rs756428491 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848376 | AAAATACAAAAATTA[C/G]CTGGGCGTGGTGGTG | 257397 |
rs756470890 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885156 | GTGTACTATTAATAC[A/C]TACCATTTCAGTGAA | 257397 |
rs756504725 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850843 | TCTCCACTTCCAATG[A/G]AAAACAAAAAAAAAC | 257397 |
rs756510616 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30853326 | TTTAGGTCTACTATT[A/G]GCTAATCCAATAATC | 257397 |
rs756552852 | snp | C/T | 3.26445e-05 | 0.00403995 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831384 | CTTTTCTTCTGGTAG[C/T]GCTCAAAGTTTCACT | 257397 |
rs756578905 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30875118 | AGTCATGGGGTCAGG[A/G]TATTATATGACTTAC | 257397 |
rs756585121 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30850785 | TCTGGGGCTTTTTTC[-/T]TTTTTTTTTTTTTTA | 257397 |
rs756609862 | snp | A/T | 2.89042e-05 | 0.00380148 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859580 | AAGCTGTGGGCTGCT[A/T]TGCGCCATGCCAGAG | 257397 |
rs756662403 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30882612 | GCCTTCGAGTATGTG[C/T]AGAAAACTTAAAACT | 257397 |
rs756680457 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842779 | TGCAATGAGCCATGA[C/T]CACACCACTGCACTC | 257397 |
rs756699781 | snp | C/G | 2.28126e-05 | 0.00337724 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854559 | TGAGAAGGTTCAACT[C/G]TAATTTCTATCTTCT | 257397 |
rs756721671 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30875424 | GTTCATTGATTAGGT[A/T]GTTTGAGGGTTCTCA | 257397 |
rs756736313 | in-del | -/CAC | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844970 | GGGATCACAGGCACA[-/CAC]CACCACACCTAGCTA | 257397 |
rs756750830 | snp | A/T | 0.0173306 | 0.0914601 | intron-variant | TAB3 | GRCh38.p7 | X:30868423 | ATATATATATAGCTT[A/T]TATATATATATAGCT | 257397 |
rs756761502 | in-del | -/GCC | | | utr-variant-5-prime, cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30889260 | GATCCGGTGTGAGCC[-/GCC]GCCGCCGCCGCCGCC | 257397 |
rs756789104 | snp | A/G | 2.48979e-05 | 0.00352822 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854870 | TGGATAAACAGGTAA[A/G]GGACGCTGGCTATAG | 257397 |
rs756790101 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877537 | AGGTGCTTTAATATT[C/T]TTGCTTCAACTAGGA | 257397 |
rs756835723 | snp | C/G | 6.22617e-05 | 0.00557915 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831408 | TTTCACTTTCAACCT[C/G]GCGCAGACTTTTCTG | 257397 |
rs756839415 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30868819 | TAATTGATCTCCTGA[A/G]TCAACTTCATTTTAC | 257397 |
rs756845019 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30876316 | TTTTTCAAATACAAT[C/G]CCCAGCATGCAATTA | 257397 |
rs756845085 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888013 | CATAAAACACACCAT[C/T]ACAAAACTTACCATG | 257397 |
rs756859117 | in-del | -/C | 0.00581083 | 0.0535878 | intron-variant | TAB3 | GRCh38.p7 | X:30853090 | ATGCTGCCTCCACAT[-/C]TGCTTCAATTTAGCC | 257397 |
rs756999846 | snp | A/G | 7.40037e-05 | 0.00608247 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831560 | CGAGGACTTTGTGTG[A/G]AGCCAGTTCGATGCT | 257397 |
rs757004675 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836003 | CTGTGCTAAACTATA[G/T]GTACTTTTAGAAAAC | 257397 |
rs757005764 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30863380 | CAGAAAATATTCCAG[C/G]CAATAAATTAAGTCA | 257397 |
rs757009535 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30838049 | TTTATTCCTATACCA[A/G]TATCACACTGTGGTT | 257397 |
rs757036813 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844828 | ATCTTTAATCTCTCG[C/T]TCTTTGTTTTTTAGA | 257397 |
rs757065838 | in-del | -/C | 0.00158814 | 0.0281345 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831009 | TGGTTTTCCAGAGAG[-/C]GGTGACCAGGTAAGT | 257397 |
rs757119745 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852421 | TTAAAAAATATATAT[A/G]TCATATGCTTAGAAG | 257397 |
rs757122616 | snp | A/G | 2.71319e-05 | 0.0036831 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846519 | AAATACCACACTATT[A/G]CTTATGGTTTACCAA | 257397 |
rs757148039 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831880 | TTCCAGCCAAATGAA[A/G]AAAAAGAGAAATGTT | 257397 |
rs757164712 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30874167 | ACAGAGTGAGACCCT[C/G]TCTCAAAACAACAAT | 257397 |
rs757164866 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863791 | TTTACAGTGACATAA[C/G]AATGGCCTAATATAG | 257397 |
rs757201499 | snp | G/T | | | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827047 | AAATGTTACCTACTA[G/T]AATTCATTTGTGGTA | 257397 |
rs757274785 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30833253 | GGATTACAGGTGTGA[A/G]CCACCGCACCCGGCC | 257397 |
rs757341077 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853823 | GGGATTGCAGGCATG[C/T]GCCACCACACCCAGC | 257397 |
rs757343275 | snp | A/G | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30874420 | TCTTGGAAAAAAGAG[A/G]AGTAAGGAGATGAAA | 257397 |
rs757368993 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841953 | AGCTGGGATTACAGG[C/T]GCGCGCCATCAGGCC | 257397 |
rs757373577 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30832270 | GGCAACCTTATGTTG[C/G]TCCCCAGGATTTGAA | 257397 |
rs757399989 | in-del | -/TATA | | | intron-variant | TAB3 | GRCh38.p7 | X:30868499 | TATATATATATAGCT[-/TATA]TATATATATATAGCT | 257397 |
rs757471545 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30865195 | AATGAAAGGTATTTA[A/G]CATTCTGGCCCCGCC | 257397 |
rs757494722 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869196 | CTCCTGAGTGGCTGG[G/T]ATTACAGGCACCCTC | 257397 |
rs757522874 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30861167 | CCAAACAAAAGCCTG[C/T]AGCTCTACTCAAGAT | 257397 |
rs757568881 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30882835 | AATGTTAATGTCTTC[A/G]TTTAGACAAAGGTAC | 257397 |
rs757571021 | in-del | -/AT | | | intron-variant | TAB3 | GRCh38.p7 | X:30849929 | TTTTGCAACCAACAC[-/AT]ATTTTATAAGAACAC | 257397 |
rs757576505 | snp | C/T | 2.30971e-05 | 0.00339824 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855317 | AACTAAACATATCAG[C/T]TGTTTACCTGCTGCA | 257397 |
rs757593930 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883909 | ATTGAGGCTCCCCCT[A/G]CACAGACTCTAGCCT | 257397 |
rs757629965 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859252 | CTGGGTAGAGGCCTC[A/G]GATGCCTAGAACGTT | 257397 |
rs757691361 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30849994 | ACATATATTACCTCA[C/T]ATAATCCTAAGAAAA | 257397 |
rs757747998 | snp | A/G | 0.00158814 | 0.0281345 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827388 | AGAAATATGAGTGCT[A/G]ACACTAGAACTAATT | 257397 |
rs757753043 | snp | C/T | 6.89647e-05 | 0.00587176 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852863 | ACTTCAGACTTCAAC[C/T]GCTCTAGCTCCTCTT | 257397 |
rs757755464 | snp | A/C | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30873574 | CCTGCCTCTCCTTCC[A/C]CCTCCTCCCCTTTTT | 257397 |
rs757764899 | snp | C/T | 3.18639e-05 | 0.00399136 | intron-variant | TAB3 | GRCh38.p7 | X:30854081 | ACTGCTGCCTCACCA[C/T]AGAAATTAAATTTCA | 257397 |
rs757767728 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30871094 | GAAAGATAAACTATG[C/T]AGAAATCACGGCTGA | 257397 |
rs757784318 | snp | A/C | 0.0480577 | 0.147375 | intron-variant | TAB3 | GRCh38.p7 | X:30850713 | TGAGACTCTCCATCT[A/C]AAAAAAAAAAAAAGA | 257397 |
rs757790556 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30841509 | GAAGAACAGATACTA[C/T]GTTGCAACTTATAAA | 257397 |
rs757791700 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30871733 | GAAAATTCAACTAAG[A/G]TAATTCATCCAGTTT | 257397 |
rs757889030 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830637 | TTATTTTGAAAACCA[A/G]TGGCCTTAATAAAAA | 257397 |
rs757910121 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851753 | GATTGCCCTTAGCTT[A/G]GAGAGGGTAGGAAAA | 257397 |
rs757987290 | in-del | -/T | 0.192271 | 0.243243 | intron-variant | TAB3 | GRCh38.p7 | X:30886335 | ATTATCATTTGTTGA[-/T]TTTTTTTTTTTGCCC | 257397 |
rs758029496 | in-del | -/CAAA | | | intron-variant | TAB3 | GRCh38.p7 | X:30873122 | AAACAAACCAACTAT[-/CAAA]AAACGAATTTTTTTT | 257397 |
rs758068172 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30872996 | TTAAACAATATCTCA[C/T]CAGAATGGCATAGTC | 257397 |
rs758114460 | snp | A/G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848296 | TGGGGGGCCAAGGCA[A/G/T]GTGGATCACTTGAGG | 257397 |
rs758198665 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838657 | CAGTCAGTTAATGAA[C/T]ATGGTATATCACTCC | 257397 |
rs758203367 | in-del | -/A | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30879902 | ATACAAGGTCAATAT[-/A]AAGATATAAACAAAC | 257397 |
rs758249491 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30861507 | TTGAAAACTCCAAAT[A/C]TGAAATACTAAGAGA | 257397 |
rs758253836 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30847399 | CAGGGGCACATATGA[C/G]GCACTGAAATGTGAA | 257397 |
rs758255586 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30860546 | CATTTTATAGTATTA[C/G]AGTCAGAAATGCATA | 257397 |
rs758300471 | snp | C/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890399 | CCTCCCGAGTAGCTG[C/T]GACTACAGGTGTGTG | 257397 |
rs758308855 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844644 | TTTATGTAACCCCTA[C/T]ATCATGCATAGTAAT | 257397 |
rs758309854 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871434 | ATTACCCTTCTATTT[A/T]CTGGTGAGGTTTCTA | 257397 |
rs758334202 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830332 | TCCCCTCACACTGGT[C/T]TGTTAACATATGCAA | 257397 |
rs758350016 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30842198 | TATGTAACAACTATC[C/T]AAAAATGATTCCTTC | 257397 |
rs758366059 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30864212 | TGGAGCTGTGTAGGC[A/G]GTAACCCTAGATCAA | 257397 |
rs758411677 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830441 | ATCATGAATTTATCA[C/G]AAAATTGGAAGGAAA | 257397 |
rs758418199 | snp | C/T | 2.49716e-05 | 0.00353344 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855012 | AGATTGCTTGGAATT[C/T]GTGGAAGAATTTGTA | 257397 |
rs758512400 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30849995 | CATATATTACCTCAT[A/G]TAATCCTAAGAAAAA | 257397 |
rs758513241 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30849484 | CAATGTGTGCTTTAG[C/T]AGCAAAAATGTCAAT | 257397 |
rs758514933 | in-del | -/GGAGAT | 0.0068637 | 0.0581785 | intron-variant | TAB3 | GRCh38.p7 | X:30873472 | GAGCTTGCAGTGAGC[-/GGAGAT]GGAGATCGCGCCACA | 257397 |
rs758550331 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30832916 | TTTTTTGTCTCATAT[A/G]GAGGAATAAAGCCTT | 257397 |
rs758591282 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30878097 | TAACGAACTAAATTT[A/G]TATGCAGTTGATAAC | 257397 |
rs758594189 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30833243 | CAAAGTGCTGGGATT[A/G]CAGGTGTGAGCCACC | 257397 |
rs758603668 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888424 | CACATTAACAAACTT[C/T]GGATCTTTTTATGCA | 257397 |
rs758697819 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858327 | TATTTGGTTTCACTC[A/C]GGTGGGAAGTGTCTT | 257397 |
rs758723940 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30840329 | GATATTCCTGTCTTA[C/G]ATGAGCATTTAAAGC | 257397 |
rs758752066 | in-del | -/TT | 0.0414859 | 0.13792 | intron-variant | TAB3 | GRCh38.p7 | X:30868405 | ATATATATATATAGC[-/TT]TTATATATATATAGC | 257397 |
rs758809438 | snp | C/T | 2.28191e-05 | 0.00337772 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854268 | ACTAAATTTAAAAGA[C/T]TTTCAGTCGTTGCTC | 257397 |
rs758821312 | snp | A/T | 2.4858e-05 | 0.00352539 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854141 | GGCATAGTCATCTGA[A/T]CCAGAACTAGAACTT | 257397 |
rs758879826 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834780 | TGCATGCCACTACCA[C/T]GCCCAGCTAATTTTT | 257397 |
rs758881906 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844800 | CCGTGTCTTTTGGGT[C/T]CACCTGCCACTAATC | 257397 |
rs758906724 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871314 | TATATCCCACACACA[C/T]CTAGTTATTTCTTGG | 257397 |
rs758929185 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859150 | CTGTGGTTCTCAATG[A/G]TGGGAGATTTTGCCT | 257397 |
rs758929449 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30883455 | GGAAGTTCTGTAAGT[A/C]ATAGAACAGAGATTT | 257397 |
rs758943166 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888350 | CCAAAGGTGGCAAGT[C/T]TTCTTAAATAATTTA | 257397 |
rs758953710 | snp | A/G | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827279 | AATTTTCCAATTGGA[A/G]TAATGTGCACTTAAT | 257397 |
rs758964343 | in-del | -/AAA | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848652 | TTAAACTGAGGGGGG[-/AAA]AAAAGCAGTTTCTGA | 257397 |
rs758984969 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30862558 | AGAGCGGCCAGCTCT[C/T]ACCTAGCTTTGTCAG | 257397 |
rs759019302 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30857465 | TAGACCTATGGATTA[G/T]GGGAAAACAAAAACT | 257397 |
rs759042828 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30839411 | ATGAGATAGAAAACA[A/G]AATTATGGATTTTTT | 257397 |
rs759094681 | snp | A/G | 1.64961e-05 | 0.00287189 | intron-variant | TAB3 | GRCh38.p7 | X:30859459 | AAAAACTAGAACTTA[A/G]TATCACTATCACTGG | 257397 |
rs759133517 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30848208 | GTGAAGCAGCCACCA[C/T]ACAGTTGCTCGTAAC | 257397 |
rs759180389 | snp | A/T | 0.000106276 | 0.00728879 | intron-variant, splice-acceptor-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846093 | AAAAATCCAAAAAAC[A/T]AAAACTATGATTATA | 257397 |
rs759205811 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30851182 | TCCTCACTTCTAATA[C/T]TGACTATACACGATA | 257397 |
rs759218258 | snp | A/G | 0.0100156 | 0.0700533 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833648 | CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC | 257397 |
rs759234993 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891300 | TTTCCTTATTACGTG[A/G]CAAAAGTGGACTAAT | 257397 |
rs759261159 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30831871 | TATGCTTTATTCCAG[C/T]CAAATGAAGAAAAAG | 257397 |
rs759331601 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845473 | TAATATTTTAGACTT[C/T]GTGGACCTGTGATAG | 257397 |
rs759372943 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843292 | TTAAAGGAATATTTT[C/T]CTAATTGTAAGGCTA | 257397 |
rs759439449 | snp | A/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890813 | TATTACAATTTAGAC[A/G]TTTAGAGGAATTGCC | 257397 |
rs759451173 | snp | A/G | 2.37372e-05 | 0.003445 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855448 | TACCCAGGTTAATAT[A/G]TAAAAGGCGATTTCT | 257397 |
rs759474878 | in-del | -/TATAC | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866119 | GTAAGTCTCAAGAGA[-/TATAC]TATGAGACTGAAATA | 257397 |
rs759474929 | in-del | -/GT | 0.00896606 | 0.0663524 | intron-variant | TAB3 | GRCh38.p7 | X:30875017 | ATTCCAGAGCTGGTG[-/GT]ACCATGTTCTAGAAA | 257397 |
rs759485485 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30879774 | AAACAAAAGTATAAC[A/G]TTTCGAAAGGAAGAA | 257397 |
rs759567559 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30881328 | TTTCTGTGTACTTTC[C/T]GCATATTAAACTTCA | 257397 |
rs759580714 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30841277 | AATACAAAAATTAGC[C/G]GGGCATGGTGGTGGG | 257397 |
rs759583794 | snp | A/C | | | intron-variant, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834362 | ACAACTTTTTTCCAT[A/C]TTCTCCAGTTACATC | 257397 |
rs759606865 | snp | G/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829842 | GCTAAATTAGAAGTG[G/T]GGGGGCGGTGTAGGG | 257397 |
rs759682694 | in-del | -/TA | 0.0152462 | 0.0859689 | intron-variant | TAB3 | GRCh38.p7 | X:30868567 | TATATATATATAGCT[-/TA]TATATATATATATAT | 257397 |
rs759779933 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887810 | CAGGGTGACTGAATG[C/T]AGATTATGTTCTTTC | 257397 |
rs759823210 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30867742 | TTAGGTCAGAAATAT[C/G]TTCTACAGCAACTAA | 257397 |
rs759830939 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30849808 | ATTTATTTCTTGATT[A/G]ATTTCCTACATAAGT | 257397 |
rs759866569 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832192 | CTTTTATTCTCATAT[C/T]CTTTCCTACATTTTT | 257397 |
rs759878206 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30870290 | AAATGAATAATCAGT[C/T]TCATTAACCCTGAAA | 257397 |
rs759906065 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30876792 | AAAACCGAAACTAAG[A/C]ATTCAATAAACAGGT | 257397 |
rs759911267 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835596 | GGGGAAGCTGTCTAA[A/G]CCCACTGAAGAGCAC | 257397 |
rs759938154 | in-del | -/TAATG | 0.0126344 | 0.0784702 | intron-variant | TAB3 | GRCh38.p7 | X:30887162 | ATAGTTGCCATGTAA[-/TAATG]TAATTTGAAATACTA | 257397 |
rs759959016 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30886969 | CCATAGCAGATTATG[A/G]TGGATCCCAGAAGAG | 257397 |
rs759959640 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829678 | TAGTGGATATATTTT[A/G]GGGAGTTTTTCACAT | 257397 |
rs759963794 | snp | A/G/T | 4.628e-05 | 0.00481022 | missense, synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852891 | CTTTCTCAAGTTTCA[A/G/T]TTGCTTTGCTAACCT | 257397 |
rs759988012 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863374 | TACAAACAGAAAATA[C/T]TCCAGCCAATAAATT | 257397 |
rs759991516 | in-del | -/T | 0.0126344 | 0.0784702 | intron-variant | TAB3 | GRCh38.p7 | X:30832352 | TGCTCAAAAAAGCTC[-/T]TTGCATCTAGAGTTA | 257397 |
rs760070371 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845626 | CCCTAGTTTGCTGAA[A/C]CCTCATCTATAATTT | 257397 |
rs760098880 | snp | A/G | 2.31742e-05 | 0.0034039 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854727 | TGGCCCAACTGGGAA[A/G]GTTGCACTTGATGCT | 257397 |
rs760103692 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30857886 | TTTTTAAGACATATA[A/G]TGAACACTTTTGAAA | 257397 |
rs760121281 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844737 | GTACCTGACTAGATT[G/T]CTCAATTCTCACATT | 257397 |
rs760169147 | snp | A/C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30856173 | AGATTTAAGCAAAAC[A/C/G]AATCAGTATAAAAAA | 257397 |
rs760219354 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30878925 | GAAAATATTACATCT[A/C]AAAAATGATGGGATG | 257397 |
rs760272606 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30858282 | GGAAGGTGATTGCTA[G/T]GAAGTGGTTTAAACT | 257397 |
rs760274329 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30881018 | CTCAACAATAATATA[C/T]AATGATCTATTCATA | 257397 |
rs760274474 | snp | C/T | 3.29468e-05 | 0.00405861 | intron-variant | TAB3 | GRCh38.p7 | X:30852741 | TGACAGCCAATATCC[C/T]GACCCTCCTATTAAC | 257397 |
rs760320543 | in-del | -/CTAT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848066 | CTCCAAACAGTGATG[-/CTAT]CTATCTTCCTAGGAA | 257397 |
rs760323008 | snp | C/G | 0.0168099 | 0.0901243 | intron-variant | TAB3 | GRCh38.p7 | X:30839400 | ACTATAAGTCAATGA[C/G]ATAGAAAACAGAATT | 257397 |
rs760350554 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30867415 | AATTTTTCTGTAAAA[C/T]TAAAACTGTTTTAAA | 257397 |
rs760381573 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30837042 | AGGCAAAATGACATC[-/T]TTTTTTTTTTTTTTT | 257397 |
rs760432608 | snp | C/T | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30850469 | TGGAATCCCAGCACT[C/T]TGGGAGGCCGAGGCG | 257397 |
rs760444606 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30873442 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCG | 257397 |
rs760468562 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30859935 | TATTTAAAAAAAAAA[A/G]ACAAAAAACAAAAAC | 257397 |
rs760538175 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841787 | GAATGAGGCAGAAAG[C/T]TAATCTACATTCAAT | 257397 |
rs760646328 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833576 | GTGGCTCACGCCTGT[-/A]ATCCCAGCACTTTGG | 257397 |
rs760654317 | in-del | -/GCCGCC | 0.00442231 | 0.0468145 | utr-variant-5-prime, cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30889257 | CGGGATCCGGTGTGA[-/GCCGCC]GCCGCCGCCGCCGCC | 257397 |
rs760659915 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830067 | CTATTAAGTTTCCAG[C/T]GATGCACCCTAGTGA | 257397 |
rs760674540 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30842445 | CTAAGTAAATTTATA[A/T]TGTTAACTATGTAAT | 257397 |
rs760676218 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30850954 | TAAGAAAATTTGTTT[A/G]TGCTCTACAGGTACC | 257397 |
rs760680779 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30865870 | AAAAGTGGCTGATAT[C/T]GAGGCATAACAAATG | 257397 |
rs760700377 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30833190 | TTAGCCAGGATGGTT[C/T]GATCTCCTGACCTCG | 257397 |
rs760719875 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843644 | GAGAATCTTACACTA[A/G]GTGTTAAATGTTTCC | 257397 |
rs760758803 | snp | A/G | 3.99664e-05 | 0.00447008 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859630 | TCTTAGGAAATGGAT[A/G]TTAACCGGCTTTCCA | 257397 |
rs760763012 | snp | C/T | 2.9609e-05 | 0.00384755 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846502 | GCTATTTAAGCAGCT[C/T]AAAATACCACACTAT | 257397 |
rs760802233 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844511 | CTCATGTTCTAATTT[A/C]TAGATCACAAAAGGC | 257397 |
rs760820599 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30839689 | GGTATATGGAAAATC[C/T]CCGCAACTTCCTCTC | 257397 |
rs760825823 | in-del | -/A | 0.0455357 | 0.143855 | intron-variant | TAB3 | GRCh38.p7 | X:30868554 | TATATATATATATAT[-/A]TATATATATAGCTTA | 257397 |
rs760844545 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30887771 | AGGGGAAGACTCCAT[C/G]AAATAAACATATGGA | 257397 |
rs760853568 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852683 | ACAACAACAAAAAAC[C/T]GGAACTCTGCCAGGA | 257397 |
rs760868442 | snp | A/G | 2.63078e-05 | 0.00362674 | intron-variant | TAB3 | GRCh38.p7 | X:30852984 | GAACAACATTGAACA[A/G]GCGACTGGAAAATTT | 257397 |
rs760937138 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886284 | CAATATAAATCATTT[C/T]AGAAAGGCTTTATTT | 257397 |
rs760954338 | snp | C/T | 2.2905e-05 | 0.00338408 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854200 | CCCCAGAGCCTGGTA[C/T]CACTGAAATGGGCTG | 257397 |
rs760995460 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30865157 | AGCACAAGAATTCCT[C/T]GTCATGCAAGACTAT | 257397 |
rs761059782 | in-del | -/AA | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30862365 | TAACTCCAGCTTTCC[-/AA]CAATGGCTCCCAAAA | 257397 |
rs761067251 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830690 | CATCTCTTATGTGGC[A/G]TAAGTAGGTCTTAGT | 257397 |
rs761120896 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852075 | TATACGCACAAAACT[A/G]CTAAATGTTGAAAGG | 257397 |
rs761136256 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30886727 | GGTGGAGGATGACTA[A/C]CAGACATTTAGTATC | 257397 |
rs761254382 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30853512 | TTTAGTCCATTCTCC[A/C]TGAATCTCTTTTTTC | 257397 |
rs761283702 | snp | C/T | 2.36022e-05 | 0.00343519 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834083 | TGGGTGTCATGGATG[C/T]CTGCCTGTACTTTGG | 257397 |
rs761287344 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848822 | TCCAAAGCTGGCATA[C/G]ACCAGCGTCAAAGAC | 257397 |
rs761370791 | in-del | -/GCC/GCCGCC | 0.0744908 | 0.180306 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30889256 | CGGGATCCGGTGTGA[-/GCC/GCCGCC]GCCGCCGCCGCCGCC | 257397 |
rs761404905 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846268 | AGAATTAAAACCCAT[C/G]AATTTATAAAATATT | 257397 |
rs761411249 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30856987 | AGCTTTAGGAAGTTT[A/T]AAAAAAAGTCCAGCA | 257397 |
rs761429855 | snp | C/T | 0.000104263 | 0.00721946 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855000 | GGAGACCCATAGAGA[C/T]TGCTTGGAATTTGTG | 257397 |
rs761470446 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886014 | TGGAAAGTAGAGAAA[A/T]TTGAAGCAGGGAGGG | 257397 |
rs761474245 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30872401 | TTCCCTGCCACCCTA[C/T]CTTTTCTCAATAGGA | 257397 |
rs761516345 | snp | C/T | 2.28009e-05 | 0.00337638 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855131 | TGAAGGAGGTGGCGG[C/T]GGTGGTGAAGGCCCT | 257397 |
rs761523591 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30882286 | TCAATCATAACTATG[A/G]TGAGTACTAAAAAAT | 257397 |
rs761542321 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30877089 | GCATCCTGATGGAGG[A/G]GCAGCAGGGGCAGAG | 257397 |
rs761571546 | snp | A/G | 0.00105904 | 0.0229869 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828150 | GAGGACAATTCTTCT[A/G]TGCCTTATATTCTTT | 257397 |
rs761610078 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30865014 | CCTGGCCTTGCTTCA[C/T]TCATCTAGATACCTG | 257397 |
rs761626979 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30883538 | AGCCTTTTAAGGAGC[A/C]AAGCCAGAAAAAAGC | 257397 |
rs761646327 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30835998 | CCAATCTGTGCTAAA[C/T]TATATGTACTTTTAG | 257397 |
rs761689647 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30849712 | CAATTCTGACTCCCA[A/G]GCCTATGTGGGCTCT | 257397 |
rs761746434 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30853071 | CTCATGTCTTTCTAA[A/T]GCTATGCTGCCTCCA | 257397 |
rs761762289 | in-del | -/TA | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30832395 | TGTCTTTTAGGTCTC[-/TA]TTGAGACTGAGGTCA | 257397 |
rs761789619 | snp | C/T | 2.30992e-05 | 0.00339839 | intron-variant | TAB3 | GRCh38.p7 | X:30852774 | ATCCTAACAGATCAC[C/T]TACCGTAGGGATCGC | 257397 |
rs761804369 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30848128 | ACCTGAAAAGGATTA[C/T]CTATTCCATAGGTTT | 257397 |
rs761849098 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841087 | GCCAAATCTGGCACT[C/T]GGCAGTCATCCACTA | 257397 |
rs761850945 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850353 | TTTGAAATTATAATA[A/C]AAGTTAAAACTAAAT | 257397 |
rs761867992 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842717 | CCACACACCAGCTAC[G/T]TGGGAGGCTGAGGCA | 257397 |
rs761891315 | snp | G/T | 2.28001e-05 | 0.00337632 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854431 | GACTAGATATCCCTC[G/T]TGAAGGAGAACTTGA | 257397 |
rs761915996 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875630 | GCATCCTAATTTCAA[C/T]AGCAATTAAGAGGGA | 257397 |
rs761922950 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851303 | TAAAGTTCAAGCACC[C/T]TGACCTAGCATTCAA | 257397 |
rs761941878 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851970 | TATACAGCACTTACC[A/G]CACTGTATTATAATT | 257397 |
rs761953940 | snp | A/T | | | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854492 | TTGATTCCATGGAGA[A/T]GGTTGATTACTGATG | 257397 |
rs761956021 | snp | C/T | 6.84314e-05 | 0.00584902 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854238 | TCTGGTGCTGCAGAG[C/T]GCTCTTCTTGGTCCA | 257397 |
rs761958396 | in-del | -/GAGC | | | intron-variant | TAB3 | GRCh38.p7 | X:30868616 | AGAGAGAGAGAGAGA[-/GAGC]GCGTGGGGGGGAGAG | 257397 |
rs761991223 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862120 | GCACATGGCCTAGCA[C/T]AGGCTAGCTGTTCAA | 257397 |
rs762000171 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834876 | GCCTCAAGTGATCCT[C/G]CCACCTCAGCCTCCC | 257397 |
rs762015412 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30885721 | ACTTTCCTCCTTGGT[A/G]TTTAAGGAGAGGGAA | 257397 |
rs762093513 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845343 | AAAGTTAGTTAGATA[A/G]AGACCTAATTTTTAC | 257397 |
rs762097688 | snp | A/C | 2.35015e-05 | 0.00342786 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834109 | TTTGGAGGTCACGCT[A/C]ATTCTTCGGGCTTTT | 257397 |
rs762141583 | snp | A/G | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884028 | TTTATACCTAACAAA[A/G]GGAATGGTGTTACTG | 257397 |
rs762146906 | in-del | -/AGG | 2.28089e-05 | 0.00337697 | cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855206 | TTGAGGTGGTTGTGA[-/AGG]AGGAGTAGCTGCACT | 257397 |
rs762196481 | snp | C/T | | | intron-variant, synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836663 | GCCCGGGCAACATGG[C/T]GAAACCCTGTCTCCA | 257397 |
rs762197972 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885063 | TAGAAATTCTTCATT[A/G]ACAATCTAAAAAGCC | 257397 |
rs762200457 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870263 | CTAATATATTTAAAA[C/G]ATTTTTTTAAAAAAT | 257397 |
rs762211348 | snp | G/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843979 | CTTCATTTCCAGATC[G/T]ACTTTTTTTTTTCCC | 257397 |
rs762263228 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30872662 | CTAATAATAGCAGAA[A/G]TGACCAAATTGAACA | 257397 |
rs762293639 | snp | G/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891248 | CACAAACCCATGAGT[G/T]AGAAATAAATGCTTA | 257397 |
rs762294840 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869473 | GTTGATTATCACTTT[C/T]AGCACTTAGTATATT | 257397 |
rs762318764 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30864840 | ACATTTAAAACTGGG[A/T]GACATCACATAAAAA | 257397 |
rs762337968 | snp | A/G | 3.30458e-05 | 0.0040647 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842940 | ACATTTATTTCTATC[A/G]TATTTGTGACATTTT | 257397 |
rs762365794 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30841052 | TTTCGGCAAGAAACT[A/G]CATATGATGCTGCCA | 257397 |
rs762372108 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830609 | TTATAAAATCATACT[C/T]TGTAAGGACTTGTTA | 257397 |
rs762373519 | snp | C/T | 2.28248e-05 | 0.00337815 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855164 | CATAGCAGACGGATT[C/T]ATTCCTGTTTGCATG | 257397 |
rs762373761 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30847394 | CCTTTCAGGGGCACA[C/T]ATGAGGCACTGAAAT | 257397 |
rs762393805 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30872988 | GAAACAAGTTAAACA[A/G]TATCTCACCAGAATG | 257397 |
rs762406825 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885132 | AAATCTAATTCTGGA[C/G]AGCTAAAGGTGTACT | 257397 |
rs762420924 | in-del | -/ATG | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30849534 | TACACAAGTGGGACA[-/ATG]ATAAGGCTAGCCATC | 257397 |
rs762423463 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830015 | ATTCTGAGCTAAGAA[A/G]GAACTCCAACAATGG | 257397 |
rs762448747 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831786 | ATTACTTTTTTTCTG[C/G]TATAAGAAGATGGAT | 257397 |
rs762543487 | snp | C/T | 0.000557508 | 0.0166866 | intron-variant | TAB3 | GRCh38.p7 | X:30852942 | GTAACAGCAAGGCTA[C/T]AGCATTATAGATAAT | 257397 |
rs762562015 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30875153 | AGAAGAAAGCATAAT[A/C]TGATAAAACTGGGAA | 257397 |
rs762566176 | snp | C/T | | | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30826945 | GCCTTCCTCCCACCT[C/T]GACCTCCCAAAGTGT | 257397 |
rs762574909 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840544 | ATCTCATCTTGAATT[C/T]CCACATATTGTGGGA | 257397 |
rs762611231 | in-del | -/CC | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30832272 | CAACCTTATGTTGGT[-/CC]CCAGGATTTGAAAAA | 257397 |
rs762665956 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887962 | CACACTGACTAAAAA[G/T]CATGTATATGTATGT | 257397 |
rs762672827 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30881739 | CTCCCTAATTTTACA[A/G]ATGAAGAAACCGAGG | 257397 |
rs762699428 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30881234 | GAGGGGGGTAAGGTA[A/G]TAAGAATTTCTTGAT | 257397 |
rs762753525 | snp | C/G/T | 4.61396e-05 | 0.00480292 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854188 | TTCCCTTTTCTCCCC[C/G/T]AGAGCCTGGTATCAC | 257397 |
rs762762019 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828673 | GAAATAATGTAAAAT[A/G]TATAGTCAGGCCTAT | 257397 |
rs762768441 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30871387 | TGGCACCTGAGTAGG[A/G]TTAGCCCCTTTTATT | 257397 |
rs762778313 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30857754 | TACAAAGAAAACTAC[C/T]AGAATAGATTCTAAT | 257397 |
rs762814473 | snp | C/G | 2.53418e-05 | 0.00355953 | intron-variant | TAB3 | GRCh38.p7 | X:30852969 | TAATGTCATTGCAGA[C/G]AACAACATTGAACAA | 257397 |
rs762856848 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30882193 | ATTGTTGCCACAAAT[A/C]GAAACCAAGGATTTT | 257397 |
rs762990305 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863140 | ATCTAAACTGGTAAA[C/T]ACATATCCTTCTTAA | 257397 |
rs763006182 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850589 | TGGTGGCACACTCCT[A/G]TAATCGCAGCTACTC | 257397 |
rs763008137 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30860895 | ATTCCTATTTTTCGG[A/T]ATTAGACAATGAAGC | 257397 |
rs763036289 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842517 | TCAAATTACCTCTGA[C/G]AGTAATTCTAAGAGT | 257397 |
rs763065102 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885620 | GGATGGCAGCTGAAA[A/G]GAGTGAGGAAACAGT | 257397 |
rs763089022 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30871009 | GCCTAAGTATTTAAT[C/T]CACAGCACATACCCA | 257397 |
rs763106409 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30872126 | CTGCATCCCTGGAAA[A/G]CCATCAGGAGTCCCT | 257397 |
rs763135028 | in-del | -/TATTT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870018 | TCAAATATGGTGATA[-/TATTT]TAAGTTATACAAGGA | 257397 |
rs763136377 | snp | A/G | 2.28985e-05 | 0.0033836 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854679 | TGATATGGATGGGGT[A/G]GAGTAGTTGAAGGAC | 257397 |
rs763138178 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30851194 | ATATTGACTATACAC[G/T]ATATTACAAAAAAGT | 257397 |
rs763138676 | snp | A/G | 2.60237e-05 | 0.0036071 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859511 | GCACTGAGACACCAC[A/G]CCCTCTGGAATTTCA | 257397 |
rs763146339 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853368 | AATCCAGTAATTCCA[C/T]TTTTATATATTATTA | 257397 |
rs763166308 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30851130 | CATTAAAGATAACTT[C/T]GTTATTTTCCAGTGC | 257397 |
rs763314510 | in-del | -/AG | 0.0246487 | 0.108244 | intron-variant | TAB3 | GRCh38.p7 | X:30868637 | GTGGGGGGGAGAGAC[-/AG]AGAGAGAGAGAATTG | 257397 |
rs763326647 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30858030 | ACATTTTAATGTGAA[G/T]AAAGCAGTTTTCCAG | 257397 |
rs763373606 | in-del | -/C | 0.0026455 | 0.0362733 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30826982 | TACAAGCATAAGCCA[-/C]CGTGCCCAGCCTGGA | 257397 |
rs763390275 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30841577 | TAGAAAACTATTCAA[C/G]CAAAATTTAAGTAAT | 257397 |
rs763392857 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30869382 | TGTTTTTTGCCATCC[A/C]ACATTTATGTTAACC | 257397 |
rs763397386 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant, frameshift-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846075 | GTAGTATACTTCTGT[-/A]AAAAAAATCCAAAAA | 257397 |
rs763414821 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853477 | TTTAGAAAAGATTCA[A/C]ATTCTTTCGTTTGAT | 257397 |
rs763434824 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877403 | AAGTTCAAATAAGCA[A/C]GTGAAATCTAAAGGA | 257397 |
rs763447650 | snp | C/T | | | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30826960 | CGACCTCCCAAAGTG[C/T]TGGGATTACAAGCAT | 257397 |
rs763506132 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30838166 | ATAGTGCTGCAATCA[C/T]GGCTCACTGCAGCCT | 257397 |
rs763561305 | in-del | -/AAC | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30836849 | CCTGTCTCAAAACAA[-/AAC]AAACAAACAAACAAA | 257397 |
rs763574602 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831797 | TCTGCTATAAGAAGA[C/T]GGATATATGTCCAGA | 257397 |
rs763580207 | snp | A/G | 4.56059e-05 | 0.00477502 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854454 | GAACTTGAAGGTGGC[A/G]TGGTGGCTGTGTACA | 257397 |
rs763599992 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877450 | ATAATGTCTTGTAAG[A/G]TTTAAAATACATACA | 257397 |
rs763610847 | snp | C/G | 2.6595e-05 | 0.00364648 | intron-variant | TAB3 | GRCh38.p7 | X:30852987 | CAACATTGAACAAGC[C/G]ACTGGAAAATTTCGA | 257397 |
rs763630281 | snp | A/G | 2.34143e-05 | 0.00342149 | intron-variant | TAB3 | GRCh38.p7 | X:30852742 | GACAGCCAATATCCC[A/G]ACCCTCCTATTAACA | 257397 |
rs763659555 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30876963 | AGAAGGAAAAGAGAC[A/G]GAATGGGGCAGAGGC | 257397 |
rs763669854 | snp | C/G | 2.38155e-05 | 0.00345068 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854819 | GATCTGCTGCTGTTT[C/G]GGAGAATACTGAGAA | 257397 |
rs763721446 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841057 | GCAAGAAACTGCATA[C/T]GATGCTGCCAAAGTG | 257397 |
rs763742404 | snp | A/G | | | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855056 | AGTCTGTCCAGAAGG[A/G]AGGTTCTGGGATACT | 257397 |
rs763783170 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30864738 | GGTTGCAAACCAATG[G/T]TCTGTGGAATGAATT | 257397 |
rs763788868 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828772 | TGATCCAGCTGGCAC[C/G]TCAGCAGCCAGGCGT | 257397 |
rs763907324 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840655 | GGAGAGTTTTCCTGC[A/G]CAAGCTCTCTTTAAG | 257397 |
rs763908754 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887972 | AAAAAGCATGTATAT[A/G]TATGTGCCTGTATTC | 257397 |
rs763935112 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848800 | TAAAAAATGGTAAGC[-/T]TTTTTTTCCAAAGCT | 257397 |
rs763946366 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30860967 | AGAAAAAAATATATG[C/T]ACATGTGTACATACA | 257397 |
rs763946457 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883826 | GAATCTGAACACTAT[C/T]ATGTGACATTTTTCT | 257397 |
rs763968793 | snp | C/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845729 | GACTTTTTTCAGTTG[C/T]TTTCACCCATATCTA | 257397 |
rs764007813 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30872370 | CAATCTTTTCTTCTG[-/T]TTTTTTTGTTTGTTT | 257397 |
rs764018950 | snp | A/C | 2.63831e-05 | 0.00363192 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859504 | GTAACATGCACTGAG[A/C]CACCACGCCCTCTGG | 257397 |
rs764020644 | snp | A/G | 5.45777e-05 | 0.00522359 | synonymous-codon, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831448 | GTACCGTGGCATCTC[A/G]CACTGCTCACAGCGA | 257397 |
rs764038111 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30841934 | ATGCCTTAGCCACCT[A/G]AGTAGCTGGGATTAC | 257397 |
rs764108966 | snp | A/C | 2.936e-05 | 0.00383133 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846504 | TATTTAAGCAGCTTA[A/C]AATACCACACTATTA | 257397 |
rs764136868 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30872249 | TTAAAGGACTCCGTG[A/G]TGAGTCTGATGTAGT | 257397 |
rs764198053 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30833248 | TGCTGGGATTACAGG[C/T]GTGAGCCACCGCACC | 257397 |
rs764198662 | snp | C/T | 5.30941e-05 | 0.00515211 | intron-variant | TAB3 | GRCh38.p7 | X:30852986 | ACAACATTGAACAAG[C/T]GACTGGAAAATTTCG | 257397 |
rs764317111 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30881755 | ATGAAGAAACCGAGG[A/T]CTTTTGAAGTTGGGT | 257397 |
rs764325914 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30851198 | TGACTATACACGATA[C/T]TACAAAAAAGTCACT | 257397 |
rs764328627 | snp | A/G | 6.46099e-05 | 0.00568338 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831391 | TCTGGTAGTGCTCAA[A/G]GTTTCACTTTCAACC | 257397 |
rs764340054 | in-del | -/A | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829982 | CACCAAAATGAGGGG[-/A]AAGATTCCAAAACTC | 257397 |
rs764378779 | snp | C/T | 0.000171268 | 0.00925229 | intron-variant | TAB3 | GRCh38.p7 | X:30852950 | AAGGCTACAGCATTA[C/T]AGATAATGTCATTGC | 257397 |
rs764381892 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846244 | ATAATATGAACTCTA[C/T]TAAGTTTTAGAATTA | 257397 |
rs764389218 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30832211 | TCCTACATTTTTGGC[A/T]TTAAAAATCCTTCAT | 257397 |
rs764401479 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866129 | AGAGATATACTATGA[G/T]ACTGAAATAATATTA | 257397 |
rs764401480 | in-del | -/CCATG | 0.00896606 | 0.0663524 | intron-variant | TAB3 | GRCh38.p7 | X:30875020 | CCAGAGCTGGTGGTA[-/CCATG]TTCTAGAAATGGGGT | 257397 |
rs764444070 | snp | A/C | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834789 | CTACCACGCCCAGCT[A/C]ATTTTTTAAATTTTA | 257397 |
rs764516087 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30836894 | AAGGTACTTGTAGAG[C/T]GCTAGATGAAGCTTG | 257397 |
rs764528040 | in-del | -/GAA | | | intron-variant, cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835584 | CTGATGAAGGTTGGG[-/GAA]GCTGTCTAAGCCCAC | 257397 |
rs764580782 | in-del | -/AAAA | 0.00126984 | 0.0251656 | intron-variant | TAB3 | GRCh38.p7 | X:30859685 | AGTCATTTTCTATTT[-/AAAA]AAAAAAAAAAAGTAT | 257397 |
rs764595833 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883807 | ATATGTTGGGCTGGC[C/T]TGGGAATCTGAACAC | 257397 |
rs764636081 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859226 | AACTGCGGGGATGCT[A/G]TTGTTATTTACTGGG | 257397 |
rs764658438 | in-del | -/A | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830875 | TGGAAATTACCCCTG[-/A]AAAAAAGCAGCAATT | 257397 |
rs764665412 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30871038 | CATGCTGGATACTAG[G/T]AAACAGATGTTATAA | 257397 |
rs764677107 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30838167 | TAGTGCTGCAATCAC[A/G]GCTCACTGCAGCCTC | 257397 |
rs764679564 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828734 | TAAAGAAACCTCTTA[C/G]AAGAAACAAGAAGTG | 257397 |
rs764728959 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887029 | GGTCCAAAACCTTTG[A/T]ATCAAATTATTAAAG | 257397 |
rs764764014 | snp | C/T | 2.56782e-05 | 0.00358308 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855004 | ACCCATAGAGATTGC[C/T]TGGAATTTGTGGAAG | 257397 |
rs764856572 | snp | A/G | 2.28014e-05 | 0.00337641 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855132 | GAAGGAGGTGGCGGT[A/G]GTGGTGAAGGCCCTT | 257397 |
rs764856579 | snp | C/T | 2.475e-05 | 0.00351773 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831564 | GACTTTGTGTGGAGC[C/T]AGTTCGATGCTCTGA | 257397 |
rs764889305 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831675 | ACCACAAAAATCAAG[A/G]GAGGTAATTGCCTAC | 257397 |
rs764900271 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844317 | AAAACCTTAATAGTG[A/G]TTTCCCTTGCAGGCC | 257397 |
rs764974337 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852246 | GCAGTTCCCTTTAAG[A/T]CTGCTATCAATCAAT | 257397 |
rs764986901 | snp | A/G | 6.8975e-05 | 0.0058722 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852784 | ATCACTTACCGTAGG[A/G]ATCGCAGTGGTGCAG | 257397 |
rs764994778 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890115 | CAGCTACTGAGGAAA[C/T]GCTGTGATCTCAGGG | 257397 |
rs765015967 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30832008 | TAAACATCTGACTAA[A/T]TGTGTGCCTTCTTCC | 257397 |
rs765036140 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30881523 | AGGTGTCAAACCAAC[C/T]AGTGACTCTCAAACT | 257397 |
rs765040785 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846520 | AATACCACACTATTA[C/T]TTATGGTTTACCAAA | 257397 |
rs765052316 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30848219 | ACCACACAGTTGCTC[A/G]TAACGAAAACATACT | 257397 |
rs765064333 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30868941 | TTACTTTGATTATCC[-/A]AAAAAAAAAAAAACT | 257397 |
rs765095171 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30860147 | GGGAGCCGTGTGTCC[A/G]TATCAATGAAGATAG | 257397 |
rs765101078 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30881191 | TCTGTGGTGTTAGAA[A/G]TTAGGACAATATGCA | 257397 |
rs765128960 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867038 | TTTGTGGTCTTCCTC[C/G]TTAAAACCCATAACC | 257397 |
rs765140646 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833673 | CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCCG | 257397 |
rs765168807 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828592 | AAACTACTCCAAAAT[G/T]TAAGGGGCAATGTAC | 257397 |
rs765227514 | snp | C/G | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890906 | AGTGGGGCTCAAGAC[C/G]TTGTCTCTGCAAGTG | 257397 |
rs765227529 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30879779 | AAAGTATAACATTTC[A/G]AAAGGAAGAAACAAG | 257397 |
rs765254479 | snp | C/T | 0.00112277 | 0.0236669 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859636 | GAAATGGATGTTAAC[C/T]GGCTTTCCAAAAGTA | 257397 |
rs765309391 | in-del | -/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858787 | GTAGGCCAACTTCTC[-/T]GTTTGTTGTCCCCTG | 257397 |
rs765336959 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30850428 | TCAAGAAGATAGATC[-/G]GGGGCCAGGTGCGGT | 257397 |
rs765342606 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841242 | CCTCGCCACCATGGT[A/G]AAACGCCGTCTCTAC | 257397 |
rs765406638 | snp | C/T | 2.28011e-05 | 0.00337639 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854442 | CCTCTTGAAGGAGAA[C/T]TTGAAGGTGGCGTGG | 257397 |
rs765465430 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30850509 | CAAGGTCAGGAGTTC[A/G]AGACTAGCCTGGCCA | 257397 |
rs765481030 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30867766 | CAACTAAATTCTACA[C/T]TATCCCACAGAAGAG | 257397 |
rs765495656 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30873449 | AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 257397 |
rs765534349 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30870443 | CTTGGCGATACAGAA[G/T]ACCCATGTCCTCGTA | 257397 |
rs765540122 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876234 | CCCTTAAGCAGATGT[A/C]CACACACACACATAC | 257397 |
rs765656042 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844751 | TGCTCAATTCTCACA[C/T]TCAAATTTGCTTCTG | 257397 |
rs765708885 | snp | C/G | 2.35682e-05 | 0.00343272 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852921 | TCTCCATCCTTGCTC[C/G]TTGATGTAACAGCAA | 257397 |
rs765765543 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30841341 | AATCACTTGAACCTG[A/G]GAGGTGGAGGTTGCA | 257397 |
rs765776038 | in-del | -/GC | 0.0015949 | 0.028194 | intron-variant | TAB3 | GRCh38.p7 | X:30868385 | GCTTATATATATATA[-/GC]TTATATATATATATA | 257397 |
rs765800869 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886508 | AAACAGTCTCTAAAG[C/T]TACATAATACACACA | 257397 |
rs765815692 | in-del | -/CAGA | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30877277 | ATTAAAATACAGGCT[-/CAGA]CAAATAAAAACAGAG | 257397 |
rs765833075 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848137 | GGATTATCTATTCCA[C/T]AGGTTTTAGGGAGTT | 257397 |
rs765849096 | snp | A/G | 2.37389e-05 | 0.00344512 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855439 | GAGAATGGATACCCA[A/G]GTTAATATGTAAAAG | 257397 |
rs765856377 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888298 | GATTGACAAACGTCA[C/T]TGAAGAAACACATCG | 257397 |
rs765871016 | snp | C/T | 2.28118e-05 | 0.00337718 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855185 | TGTTTGCATGGAAGA[C/T]GGCTGTTGAGGTGGT | 257397 |
rs765932284 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871251 | CAGTTATTTAACATG[A/G]ATTTGAGAATAAGAA | 257397 |
rs765936690 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30879651 | ATCATATTTAATGGA[A/G]AAATGTTCAAAGTTT | 257397 |
rs765983728 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30881074 | AATGAACAGTCTACA[A/G]CTACATACGATATAA | 257397 |
rs765987246 | in-del | -/AT | 0.000135623 | 0.00823365 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834003 | TCTACATGGATTAAC[-/AT]GTGTCTTTGGACATT | 257397 |
rs766005539 | snp | A/C | 3.50674e-05 | 0.00418718 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842963 | GACATTTTTCATACT[A/C]ACCTTTTTTAGATGG | 257397 |
rs766112253 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30861252 | AATGATGAATCAATT[C/T]CACTATACTAAACCA | 257397 |
rs766161878 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30878594 | TAGGGACAGAGATAC[A/G]ATACAATTACCAAAC | 257397 |
rs766165523 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870494 | TATAATAGAGTGGGG[G/T]TGAGTTCTATAATAA | 257397 |
rs766209417 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30833191 | TAGCCAGGATGGTTC[A/G]ATCTCCTGACCTCGT | 257397 |
rs766224361 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30864977 | AGTTCCTATACTCCG[A/T]AGCTGATTCCAAACA | 257397 |
rs766229055 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30879016 | ACAAGGGTATAAACA[C/T]CTACCTACCCATCTC | 257397 |
rs766236824 | snp | A/C | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890035 | CTGATACTAATAATT[A/C]TTTTTCCTATTTTAT | 257397 |
rs766250782 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841814 | CAATGACTACTTATT[C/T]ATGAATGAATGAATA | 257397 |
rs766278464 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30865977 | AGGGGGAGAGGAATA[C/T]GATAGTTATTATTTC | 257397 |
rs766282594 | snp | G/T | 0.0026455 | 0.0362733 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30889304 | CTCCTCCCTCAGTGC[G/T]TCCCTCCCACCGAGG | 257397 |
rs766300991 | snp | G/T | 0.00211696 | 0.0324653 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835419 | TCGAGTCACATACCT[G/T]ATCTCACTAACTCTT | 257397 |
rs766311256 | in-del | -/TG | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30874293 | TGTGCTATTAAGAAC[-/TG]TATTGTATGTGCTGT | 257397 |
rs766366569 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30877299 | ATAAAAACAGAGTTC[A/C]TCTCCAGCAAACCCT | 257397 |
rs766385385 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853662 | TACATGACTCTGAAG[C/T]ACTAACTTTATTCTT | 257397 |
rs766425358 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844539 | GGCTTACTATAAGTA[A/T]CCTAACCAAATGTTT | 257397 |
rs766438168 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833590 | TAATCCCAGCACTTT[-/G]GGAGGCTGAGGCGGG | 257397 |
rs766485271 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30865365 | GAACTTTTAGGATTG[A/C]AAAATAAAAGAATCA | 257397 |
rs766498380 | snp | A/G | 2.29205e-05 | 0.00338522 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854685 | GGATGGGGTGGAGTA[A/G]TTGAAGGACTAGGTG | 257397 |
rs766501248 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834672 | GCTGTCCAGGCTGGA[A/G]TACAGTGGCACAATA | 257397 |
rs766536507 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30848210 | GAAGCAGCCACCACA[C/T]AGTTGCTCGTAACGA | 257397 |
rs766551382 | in-del | -/CAATT | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30882311 | AAAAATTAAATTCTC[-/CAATT]CATTTCAATTAGCTT | 257397 |
rs766630847 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30867560 | GAAATCTGAGAAAAC[A/G]AAAAGATGGTTATCT | 257397 |
rs766631232 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30886401 | CACAAGTAAGGAAGT[A/G]TATTTTATTTAACGC | 257397 |
rs766633118 | snp | A/G | 2.58248e-05 | 0.00359329 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859532 | TGGAATTTCAGGGAA[A/G]CGTTGTCGAAGATCA | 257397 |
rs766661091 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851574 | AGACCCACTTCCCAT[A/G]TTAAACACACTTATG | 257397 |
rs766669911 | in-del | -/TATAGCT | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30868561 | ATATATATATATATA[-/TATAGCT]TATATATATATATAT | 257397 |
rs766705264 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30886005 | AGGAGAGGATGGAAA[G/T]TAGAGAAATTTGAAG | 257397 |
rs766706908 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30848880 | CAGTTATGCCTCTGG[A/G]ACTCAAAGCTGTGGG | 257397 |
rs766720260 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830719 | GTTACCAGTGTTGAT[A/G]GAGCTCGATGAATCA | 257397 |
rs766793627 | in-del | -/CTTATATATATATATATATATATATATAGCTTATATATATATATATATAT | | | intron-variant | TAB3 | GRCh38.p7 | X:30868537 | TATATATATATATAG[lengthTooLong]AGAGAGAGAGAGAGA | 257397 |
rs766799594 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30874910 | TGGAAAAATTGAGAC[A/G]TGTCTAAAAAGAGAG | 257397 |
rs766805089 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852141 | CAAGATTTTAAACAT[A/G]CTTCAAAATTCTCAG | 257397 |
rs766813797 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876047 | GACAAAAGGGAAAAT[C/T]CTCTTCACCCACTTT | 257397 |
rs766849808 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867359 | TAATAATAGGGGAAA[C/T]TGAGTGCAGGGTATA | 257397 |
rs766851169 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30862398 | GGTTTTATTCATTTT[C/T]CAACCTTAATTACAA | 257397 |
rs766852468 | snp | G/T | | | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854838 | GAATACTGAGAAGGC[G/T]GATAGTTCTGTTGGT | 257397 |
rs766866675 | in-del | -/AGG | 0.000102459 | 0.00715675 | intron-variant | TAB3 | GRCh38.p7 | X:30831588 | GCTCTGAGGGAGGTT[-/AGG]ATTAAGGGGGAGGGG | 257397 |
rs766929083 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30837160 | TTCAAGTGATTCTTC[G/T]GCCGCAGCCTCCCAA | 257397 |
rs766934292 | in-del | -/TA | 0.00475684 | 0.0485365 | intron-variant | TAB3 | GRCh38.p7 | X:30875122 | ATGGGGTCAGGATAT[-/TA]TATGACTTACAGAAA | 257397 |
rs766936620 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30886760 | TTTCTCTTTTTTTCT[C/G]ATTTCTGTGGCTGTT | 257397 |
rs766961200 | snp | C/T | 2.28762e-05 | 0.00338195 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854673 | CCTTGTTGATATGGA[C/T]GGGGTGGAGTAGTTG | 257397 |
rs766985144 | snp | A/G | 0.000162549 | 0.00901376 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846114 | TATGATTATAGTTGA[A/G]TGTTTTCACATAACA | 257397 |
rs767014899 | snp | A/C | 3.24507e-05 | 0.00402794 | missense, intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843027 | GTCATAAAAATTATT[A/C]ATGGCTTTTGGATCA | 257397 |
rs767105642 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30858069 | GGTGGTAAATCTCCA[C/T]ACCAATATATTTTAT | 257397 |
rs767119490 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30833161 | GTTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT | 257397 |
rs767161624 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877558 | TCAACTAGGAGGAAG[A/G]TAGAAGTATCAATTA | 257397 |
rs767174491 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30857134 | AAAATGAGATCATGC[A/G]TGTAAAACATTAACA | 257397 |
rs767202471 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30877099 | GGAGGGGCAGCAGGG[A/G]CAGAGGTGGGGAGAT | 257397 |
rs767219220 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869478 | TTATCACTTTCAGCA[-/C]TTAGTATATTAACTT | 257397 |
rs767255928 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878707 | TGACCACATGCTAAG[C/T]CATAAAGTAAGTCTC | 257397 |
rs767295592 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888120 | GTTCTTGTATACTAC[G/T]GCAAATCATTACTAA | 257397 |
rs767336511 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832511 | AACACCTTTTTAAAT[A/G]GGTAACAAAAGAAAC | 257397 |
rs767366561 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30872432 | TTAGAACTGTTCGCT[A/C]AGGATTGGAAGACCT | 257397 |
rs767382738 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841135 | ATTTTTAGAAATCAA[C/T]AGACTATTTTTTGGC | 257397 |
rs767389639 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828821 | CCACTTCCATGCCAA[C/T]TGTCTGTACATACCA | 257397 |
rs767408698 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30848131 | TGAAAAGGATTATCT[A/C]TTCCATAGGTTTTAG | 257397 |
rs767434755 | snp | C/T | 4.56924e-05 | 0.00477955 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854495 | ATTCCATGGAGATGG[C/T]TGATTACTGATGGGT | 257397 |
rs767437845 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30849778 | GATGAGCAAAATGGG[A/G]AATCTGACTAAATGA | 257397 |
rs767486954 | snp | A/C | | | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855205 | GTTGAGGTGGTTGTG[A/C]AGGAGGAGTAGCTGC | 257397 |
rs767514270 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875080 | AGGAGTAATCTCCCA[A/G]TTGTCTCAATCTTCA | 257397 |
rs767549416 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843591 | CAATAAATGTGAAAT[A/G]ACATCAGCAGTTTAT | 257397 |
rs767554584 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30868374 | ATATATATATAGCTT[A/T]TATATATATAGCTTA | 257397 |
rs767582027 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884201 | TTTCATGCCCACACC[C/T]CAGAACAGAAGGCGT | 257397 |
rs767598733 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842723 | ACCAGCTACTTGGGA[A/G]GCTGAGGCAGAAAGA | 257397 |
rs767639868 | snp | C/G | 2.44648e-05 | 0.0034974 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831540 | CTTCATCTCGAGGTT[C/G]TGTCCGAGGACTTTG | 257397 |
rs767641951 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834945 | TGGATTTTTTAAAAA[C/T]AGCAGTACTTGAAAA | 257397 |
rs767671670 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867227 | TGGAATCCTGAAAGA[A/G]GAAAAAAAACATGTT | 257397 |
rs767716017 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891134 | GGTCATTCACTCCTA[C/T]CACACACCCCACATA | 257397 |
rs767765134 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30868231 | TAGCACAAAGTGTGT[A/G]TAACTTTTTGAAAAA | 257397 |
rs767783795 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886055 | TTAGAGTTGGACAAA[G/T]AGAACTGTCCATGAA | 257397 |
rs767802778 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859801 | TCCACTGACACTCCT[C/T]CTTAGTCCTGCTGCC | 257397 |
rs767806549 | in-del | -/AAAGAACACTTAAAT | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843431 | TGAACAAACTGTGAG[-/AAAGAACACTTAAAT]AATGAAAGCTTACTT | 257397 |
rs767899229 | in-del | -/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30873122 | AAACAAACCAACTAT[-/C]AAAAAACGAATTTTT | 257397 |
rs767936449 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891268 | ATAAATGCTTATTGT[A/G]GCATGGCACTGAGAC | 257397 |
rs767942379 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30885752 | GAAGAGGAGAAACCA[C/T]TGGAGGGTCTTGACA | 257397 |
rs767988970 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841561 | ATGAGCTTAATATAC[A/G]TAGAAAACTATTCAA | 257397 |
rs768041983 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30872714 | ATTACATAACTAATT[C/T]ATGCACCAGTAATCA | 257397 |
rs768050070 | in-del | -/TTCTG | 2.28022e-05 | 0.00337647 | frameshift-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855223 | GAGGAGTAGCTGCAC[-/TTCTG]TTCTGTTCGTTCATA | 257397 |
rs768080890 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884406 | AAAATGAGGGAACAG[A/G]TCAGAGATTAAGTAA | 257397 |
rs768097610 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829139 | AGGTGAAAACAATGA[C/T]TGACTAGATAATATC | 257397 |
rs768161935 | in-del | -/A | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830666 | AACATGCAGTAACTT[-/A]AAAAAATGCATCTCT | 257397 |
rs768187403 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848710 | AGTTTTCGTGCAGGA[A/G]GAATTTCAAAATTGG | 257397 |
rs768260802 | in-del | -/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848281 | TAATCCCGGCACTTT[-/G]GGGGGGCCAAGGCAG | 257397 |
rs768292349 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30865530 | GCCGTATCTGAGTAT[C/G]AAGTACTGTGCTAAG | 257397 |
rs768340451 | in-del | -/TA | 0.360916 | 0.224049 | intron-variant | TAB3 | GRCh38.p7 | X:30868499 | TATATATATATAGCT[-/TA]TATATATATATATAG | 257397 |
rs768343225 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30873912 | GGCACAGTAGCTCAC[A/G]CCTGTAATCCTAGTA | 257397 |
rs768380965 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30842133 | GCCAATTAAACATTT[C/G]CTACATAAAAATAAG | 257397 |
rs768401472 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30850092 | ATCCAAGGATACATG[A/G]GTGACAAATAGAAGT | 257397 |
rs768438489 | snp | A/G | 5.3749e-05 | 0.00518378 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854919 | GGTGAGGACTGCCAC[A/G]GCGTACTCTGAGGAG | 257397 |
rs768444478 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869113 | TCACCCAGGCTGGAG[G/T]GCAATGGCACGATCT | 257397 |
rs768496908 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30855730 | CTGAAAAGGAGACCC[A/G]AACGATTCATATTAT | 257397 |
rs768502832 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845260 | AGGAAAGCTGATTAA[C/T]ACACAGAATTAAGAA | 257397 |
rs768516766 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836425 | AAGCATCTATCTACA[C/T]AATTGAGCTACGCAT | 257397 |
rs768556150 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885498 | GCTTCCCTAGGACCA[C/T]AGACCTCGGCTTCCA | 257397 |
rs768609466 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30864889 | CTCTGAAAAATCACG[A/T]GATCTAGCAACTGCA | 257397 |
rs768632797 | in-del | -/TACA | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30860975 | ATATATGTACATGTG[-/TACA]TACAAACATGTGTAC | 257397 |
rs768645389 | snp | A/G | 0.000107406 | 0.00732743 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845955 | CAGCCTACTAGTCAA[A/G]AGTATGCAGCAGCTG | 257397 |
rs768669179 | in-del | -/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30827977 | TTTTTAAAAGTAACA[-/T]TTCAGTTGTCATTTT | 257397 |
rs768680676 | snp | A/C/T | 0.00158982 | 0.0281493 | intron-variant | TAB3 | GRCh38.p7 | X:30859360 | GAGGGAAATCCTGCT[A/C/T]CACACACACACACAC | 257397 |
rs768732658 | snp | C/T | 0.0147244 | 0.0845304 | intron-variant | TAB3 | GRCh38.p7 | X:30862034 | GGATCTTCATTTAAA[C/T]AATAGGCGACTACCT | 257397 |
rs768779977 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30876064 | TCTTCACCCACTTTC[A/G]GGTTGGGACCCTGAA | 257397 |
rs768783907 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870914 | AATACAAACATTTCA[C/T]ACAAGAAGATAACTG | 257397 |
rs768801187 | in-del | -/ATATA | 0.151636 | 0.229836 | intron-variant | TAB3 | GRCh38.p7 | X:30839920 | ATATATATATTATAT[-/ATATA]TATATATATATATAT | 257397 |
rs768841539 | in-del | -/GGT | 2.28016e-05 | 0.00337643 | cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854448 | GAAGGAGAACTTGAA[-/GGT]GGCGTGGTGGCTGTG | 257397 |
rs768858584 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30827913 | ACTGTTAATTCTTTC[A/G]AAAAGATACAGTAGT | 257397 |
rs768891944 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874498 | CCTTTCATTTGTGTA[C/T]ATTTAGAAATGTTCA | 257397 |
rs768947765 | snp | A/G | 6.84018e-05 | 0.00584775 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855129 | TATGAAGGAGGTGGC[A/G]GTGGTGGTGAAGGCC | 257397 |
rs768965713 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885637 | AGTGAGGAAACAGTG[A/C]GAAGATGGCGGCCTG | 257397 |
rs769018330 | in-del | -/TAAAT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866618 | ATTTGAACACCAAAA[-/TAAAT]AAAGTAGTATTATAT | 257397 |
rs769026911 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30846943 | TAGAGCACTGAGAAT[A/C]TTTTGTGTCTATGTT | 257397 |
rs769033894 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831158 | AAGAGCTCTTGACTT[A/C]TGTGTGTACATTCTT | 257397 |
rs769035876 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30862031 | TTAGGATCTTCATTT[A/C]AATAATAGGCGACTA | 257397 |
rs769043823 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891120 | GTGGTCAGAAAGGGG[A/G]TCATTCACTCCTATC | 257397 |
rs769076238 | snp | C/T | 2.28014e-05 | 0.00337641 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854458 | TTGAAGGTGGCGTGG[C/T]GGCTGTGTACAGTGA | 257397 |
rs769088761 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845284 | TTAAGAAAAATTACA[C/T]GTCAACTTTAACGTA | 257397 |
rs769106703 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30833321 | TACCTTTTAAAAGAA[C/T]AATATGCCCAAAAAC | 257397 |
rs769121435 | snp | C/T | 0.000511158 | 0.0159787 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854182 | TATGGCTTCCCTTTT[C/T]TCCCCCAGAGCCTGG | 257397 |
rs769138074 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30838252 | ATAGGTGAGGCTGCA[A/G]TGAGCTATTTTTAAA | 257397 |
rs769150940 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30859385 | ACACACACACACACA[C/T]ACACACAAGAAAACA | 257397 |
rs769176477 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827578 | GATTTCATTCACAGC[A/G]TACACAGAAATCTAA | 257397 |
rs769227891 | snp | C/T | 0 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836195 | GAAGAAGATAAAAAA[C/T]GGGTTAAAGACAATT | 257397 |
rs769248341 | snp | G/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885358 | AAACACAGAACCTGT[G/T]TGGGCAATGTTTCTA | 257397 |
rs769301551 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30864200 | AGCTGTGGATTGTGG[A/G]GCTGTGTAGGCGGTA | 257397 |
rs769326704 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30882153 | CTGTTACATATGGTA[C/T]CCCTGAAAAAAACAA | 257397 |
rs769338652 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30879295 | AAAGCAGGTATCTTC[C/T]TTAGCTCATTTTACA | 257397 |
rs769381094 | snp | A/C | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30872171 | TGTACTAGTCATTAA[A/C]ATTTAATGAACTTGA | 257397 |
rs769411916 | snp | A/C | 2.35419e-05 | 0.0034308 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834113 | GAGGTCACGCTAATT[A/C]TTCGGGCTTTTCTCT | 257397 |
rs769416708 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841028 | ATGCTAACTATACAC[C/T]TCAGTGACTTTCGGC | 257397 |
rs769488247 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30883197 | TCTGAAACCATTCCT[C/T]AGTAGAAAGGAAAGA | 257397 |
rs769512793 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844118 | GAAAAAGGTTTAGAT[A/T]CCTTCCCTAGCTTAA | 257397 |
rs769578578 | snp | A/C | 2.68583e-05 | 0.00366448 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834015 | AACATGTGTCTTTGG[A/C]CATTCTGCACAAACT | 257397 |
rs769592771 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30847198 | TAGTAATTGGTAGAG[C/T]CAGGATTTATATAAA | 257397 |
rs769604537 | snp | A/C | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834740 | ATCCTCCTGCCTCAG[A/C]CTCCCAAGTATCCAA | 257397 |
rs769652137 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874374 | TGTTAAATTATTGGG[G/T]AGTGAAATTATGTCT | 257397 |
rs769666013 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30867953 | ACAGGCTAGAGTATA[A/G]TGGCAAACTCACGGC | 257397 |
rs769718555 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875598 | CCATGAGAGGAAAAA[A/G]TTTTAGTTGATATTA | 257397 |
rs769763624 | snp | C/T | 2.43427e-05 | 0.00348866 | intron-variant | TAB3 | GRCh38.p7 | X:30852945 | ACAGCAAGGCTACAG[C/T]ATTATAGATAATGTC | 257397 |
rs769778363 | snp | A/G | | | intron-variant, utr-variant-5-prime | TAB3 | GRCh38.p7 | X:30883633 | TTCCCAAGGCTTGAC[A/G]GTCCTTGCTAGGACT | 257397 |
rs769796691 | snp | A/C | 0 | 0 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835035 | CTGAATTCCAATTAC[A/C]TATGTGTGCAGAAGC | 257397 |
rs769810956 | snp | A/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836173 | CTACTGTTTCTAAGT[A/T]TTAACAGAAGAAGAT | 257397 |
rs769816016 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869959 | GTATGTACTAGATCA[C/T]GATTAAAATGTATTT | 257397 |
rs769848965 | in-del | -/GCT | 0.0126344 | 0.0784702 | intron-variant | TAB3 | GRCh38.p7 | X:30868479 | TAGCTTATATATATA[-/GCT]TATATATATATATAG | 257397 |
rs769851823 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838079 | TATTGTAGCTTTATA[A/G]TAAGTCCTGAAGTTG | 257397 |
rs769871245 | in-del | -/TTTG | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30869361 | CACTGCGCCCAGCCT[-/TTTG]TTTGTTTTTTGCCAT | 257397 |
rs769928836 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30847638 | CATATAAAGTGAAAA[A/G]TTAAATATCTGCTAC | 257397 |
rs769932586 | in-del | -/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30838901 | AGTTCTAATAGTTAG[-/T]TGTTTTCCAGTATCC | 257397 |
rs769974654 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30860481 | CATCACCAATGAGGG[C/T]CAGATGGACTGCACA | 257397 |
rs769988931 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845003 | ATTTTTAAAAAATTA[C/T]TTGTAGGGATGGGGT | 257397 |
rs770016099 | snp | C/T | 0.00317376 | 0.039709 | intron-variant | TAB3 | GRCh38.p7 | X:30865345 | AAGTTAGCCTTGTCT[C/T]GAGAGAACTTTTAGG | 257397 |
rs770032895 | in-del | -/AATC | 2.47234e-05 | 0.00351583 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846537 | TATGGTTTACCAAAT[-/AATC]AAGTCTATACCTCTA | 257397 |
rs770037952 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890961 | TGCTGCTATGGGAAG[A/G]AAGTTCTCCTGTCCC | 257397 |
rs770067073 | in-del | -/TTCTC | | | intron-variant | TAB3 | GRCh38.p7 | X:30873749 | TTTTAACATTTTCTT[-/TTCTC]TAGCTTACTTTATTG | 257397 |
rs770070736 | snp | G/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889744 | GTGAGAGGCGTCCCT[G/T]AAGGCTTGGTCATCC | 257397 |
rs770080569 | snp | A/G | 0.00158814 | 0.0281345 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829885 | AAACCTGATGGGAGC[A/G]TCTATGGATATTCCT | 257397 |
rs770085129 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884842 | ATGTTTACACTAAAT[-/A]AAATGAGGGTAAAAT | 257397 |
rs770090047 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30833039 | GCAGTGGCGTGATCT[C/T]GGCTCACTGCAAGCT | 257397 |
rs770161543 | snp | A/G | 4.34934e-05 | 0.00466313 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842942 | ATTTATTTCTATCGT[A/G]TTTGTGACATTTTTC | 257397 |
rs770163638 | snp | A/G | 2.49212e-05 | 0.00352987 | stop-gained, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855535 | CCTGGGAAAGGGCTC[A/G]GCAACAGGCTTCAAG | 257397 |
rs770166068 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30880455 | CATATAGGAAAAGAC[A/G]GTATTATCCCCTACC | 257397 |
rs770173245 | snp | A/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30872016 | CCTCTCTCATCACCT[A/C]GAGTGCCTAAGGTAG | 257397 |
rs770205221 | in-del | -/TGT | | | intron-variant | TAB3 | GRCh38.p7 | X:30864802 | GTGTGTGTGTGTGTG[-/TGT]TTTTTTTTTAAAGTT | 257397 |
rs770207564 | snp | A/C | 0.0121112 | 0.0768695 | intron-variant | TAB3 | GRCh38.p7 | X:30864521 | CCAACAGAATTGCTC[A/C]TCCCAATCAGAGAGG | 257397 |
rs770212579 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30832228 | TAAAAATCCTTCATA[C/T]ATCAGTTTTTAAAAA | 257397 |
rs770225305 | snp | A/G | | | stop-gained, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859540 | CAGGGAAACGTTGTC[A/G]AAGATCATGGAGAAC | 257397 |
rs770250169 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878382 | GCACGTGCCTGTAGC[C/T]CCAGTTACATGGGAG | 257397 |
rs770251437 | snp | A/G | 6.81222e-05 | 0.00583579 | intron-variant, missense, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845984 | TGTGGACATCAGTCA[A/G]TATATTTTCCACAGA | 257397 |
rs770323865 | snp | G/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889700 | CAGTCAAGAAACCCA[G/T]TAAAGGGCTTGGCAG | 257397 |
rs770364402 | snp | C/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30867730 | TCTTCTTTTCTTTTA[C/G]GTCAGAAATATCTTC | 257397 |
rs770367855 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834303 | GCAAGGGCAGGCACC[A/G]TATTTAATACTGCTT | 257397 |
rs770400084 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845641 | CCCTCATCTATAATT[G/T]TGATTGCTTTAGAAT | 257397 |
rs770402159 | snp | A/G | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30853972 | GAGCCACCGCACCCG[A/G]CCACTAACTTTATTC | 257397 |
rs770449685 | in-del | -/AC | 0.00475684 | 0.0485365 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890683 | TAATATCAAGAATTG[-/AC]ATTATTAGGCAACTG | 257397 |
rs770468665 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30883336 | CTTCTTATGCACTCA[C/T]TCATGGGTCAGATGC | 257397 |
rs770491565 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30856417 | ACTTTTGAAGTTCCA[A/G]CTGACAGTAATCAGA | 257397 |
rs770547600 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848599 | TTACTAAGGGTTTAT[C/T]AGTAAGATTCCTATG | 257397 |
rs770564699 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30842452 | AATTTATAATGTTAA[C/T]TATGTAATATAGTGT | 257397 |
rs770565935 | snp | C/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30835850 | ATATTAATTACACTT[C/G]GATTTCTGGTATATA | 257397 |
rs770605706 | snp | C/T | 5.38634e-05 | 0.00518929 | intron-variant | TAB3 | GRCh38.p7 | X:30855591 | ATGGTAAAAGTAACA[C/T]TGGCAACATTAACAA | 257397 |
rs770648735 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885094 | TATCAGTTTATCTCC[C/T]ACAAGAGCCATCTGA | 257397 |
rs770693409 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30870213 | TAGATGTGTTCATGT[A/G]GCATCCTCACGTACC | 257397 |
rs770741291 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30862169 | AATGGGGAGAAAAAA[C/G]GAATTCACTGAATTT | 257397 |
rs770746439 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30850974 | CTACAGGTACCTAAA[A/G]GTTTCCAAAGTACCC | 257397 |
rs770787206 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30871474 | GAATTGTCCAAAGAA[C/T]TTGTAACTCCCACTA | 257397 |
rs770852021 | snp | C/G | 2.28511e-05 | 0.0033801 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854319 | ACTGTAGTTGGGTTT[C/G]GTATCACTCGAGGAG | 257397 |
rs770880514 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885589 | AAGACCAACTGGGAA[A/G]GAAGGATGGAGCGGG | 257397 |
rs770902099 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866897 | AAAAAAAAAAGATTA[C/T]AGTGAAGAAACCTGA | 257397 |
rs770920914 | snp | A/G | 0.00475684 | 0.0485365 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843155 | TAAGAAGGGAAAAAT[A/G]TTTTCCAGGATTTCA | 257397 |
rs770942158 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30857770 | AGAATAGATTCTAAT[C/G]TCACATTTGACTGTT | 257397 |
rs770988576 | in-del | -/T | 0.167807 | 0.236102 | intron-variant | TAB3 | GRCh38.p7 | X:30875474 | CTCAGCAGAACTGCC[-/T]TTTTTTTTTTTTCCT | 257397 |
rs771028166 | in-del | -/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877024 | AAACCTGTCAAACCA[-/C]ATGTGTAACAATCTC | 257397 |
rs771057065 | snp | A/G | 2.54978e-05 | 0.00357047 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831493 | GTTAAGAAAGGTGCA[A/G]CTATCACAATTCCAT | 257397 |
rs771079561 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30846753 | GTATTACCAAGAATA[C/T]GGCCTTAGTCCATAA | 257397 |
rs771088514 | in-del | -/T | 0.0855902 | 0.188333 | intron-variant | TAB3 | GRCh38.p7 | X:30832974 | CATTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTG | 257397 |
rs771098103 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30842462 | GTTAACTATGTAATA[C/T]AGTGTTTCAGCTTCT | 257397 |
rs771138367 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30859125 | ACATGCTTTTATTTT[C/T]TTCTCCAATCTGTGG | 257397 |
rs771140439 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869175 | AAGCGATTCTCCTGC[C/T]TCAGCCTCCTGAGTG | 257397 |
rs771153013 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30872812 | CCTCTGATGAATCTT[C/T]ACAACACTTAAGGTG | 257397 |
rs771170079 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30841032 | TAACTATACACCTCA[C/G]TGACTTTCGGCAAGA | 257397 |
rs771185110 | snp | C/T | 0.00024775 | 0.0111271 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854952 | TGTCTTCCTGATGAA[C/T]TCTGAGATGTCTGTC | 257397 |
rs771189695 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30878021 | AATCAAAGAAAAAGG[A/T]TCACTAGAGTTAAAA | 257397 |
rs771190895 | snp | G/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30853303 | CTTTTTAAAAACTCT[G/T]TATCTAATTTAGGTC | 257397 |
rs771206865 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836458 | AGCATTCAATACATA[C/T]TTAAGAAATTTTAAC | 257397 |
rs771222366 | snp | A/G | 6.07921e-05 | 0.00551293 | intron-variant, missense, synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846063 | GAGAGCTTCTGCTGT[A/G]GTATACTTCTGTAAA | 257397 |
rs771226680 | snp | C/T | 2.32791e-05 | 0.0034116 | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846635 | TTCTCAATCTTGTCA[C/T]TTCCTCAGGCTAGTA | 257397 |
rs771274828 | snp | G/T | 2.28076e-05 | 0.00337688 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855083 | TACTGTAACAGTAAT[G/T]GGATTTGTACTATAC | 257397 |
rs771350740 | in-del | -/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30849230 | ACATCTTTGTCAGCA[-/T]TTAATATAATGCTTT | 257397 |
rs771354624 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848473 | GTTGCAGTGAGCCCA[C/G]ATTGCACCACTGCAC | 257397 |
rs771364546 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828591 | AAAACTACTCCAAAA[C/T]TTAAGGGGCAATGTA | 257397 |
rs771369956 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832124 | AGAATAGTGAAAAGA[C/G]GAAGATTCTACAGTT | 257397 |
rs771410200 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30876646 | GAGTAGCTGAGACTA[C/T]AGGCATGCACCAGCA | 257397 |
rs771518687 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866692 | CTGAGATAAAGAAAT[G/T]ACTGAATAAATGAAT | 257397 |
rs771530217 | snp | A/C/T | 9.19001e-05 | 0.00677814 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852787 | ACTTACCGTAGGGAT[A/C/T]GCAGTGGTGCAGCTG | 257397 |
rs771561000 | snp | A/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829638 | GTTTTTATCAGTGTT[A/T]ATTACCATGCTTCCT | 257397 |
rs771606950 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831284 | TCCTTTCGTGAGCAC[A/G]ACGACGACCACAAAG | 257397 |
rs771649060 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30833560 | AATTTGGCCAGGCAC[A/G]GTGGCTCACGCCTGT | 257397 |
rs771671568 | snp | C/G | 3.01841e-05 | 0.00388473 | intron-variant | TAB3 | GRCh38.p7 | X:30859477 | TCACTATCACTGGTA[C/G]GTAACTTACCTGTAA | 257397 |
rs771695474 | snp | C/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890551 | GGTGGTGAGCCACCG[C/T]GCCCAGCCAAAGAGA | 257397 |
rs771703152 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30840968 | CATTCAGGCAAAATC[A/G]AGTTTAAAGACTGAT | 257397 |
rs771749344 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30833488 | ACTGATAATTTTATA[C/T]TGATTTCATATTGAA | 257397 |
rs771754418 | snp | A/C | 2.35186e-05 | 0.0034291 | intron-variant | TAB3 | GRCh38.p7 | X:30852729 | AAATAAATGACCTGA[A/C]AGCCAATATCCCGAC | 257397 |
rs771780725 | snp | A/C | 0.00422943 | 0.0457911 | intron-variant | TAB3 | GRCh38.p7 | X:30859391 | ACACACACACACACA[A/C]AAGAAAACATACCTG | 257397 |
rs771786198 | snp | C/T | 2.28446e-05 | 0.00337961 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854369 | AGGTCCAGTTGGCTG[C/T]GTATATGTAATATAC | 257397 |
rs771837409 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829582 | CATCTGCTTTCTCAC[C/T]GTTATTTTCACAGTT | 257397 |
rs771864937 | snp | A/G | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30860343 | GAAAATCTGGATGAA[A/G]AGTAGGAAATACACA | 257397 |
rs771870211 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869926 | TACTCATTCAAAAAA[C/G]TTGTTTCAGGTATGT | 257397 |
rs771874444 | snp | C/T | 0.000159582 | 0.00893116 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854621 | GTATGGAAGATAGGC[C/T]ACTGAATGGCTTCCC | 257397 |
rs771881829 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30880938 | AAAAGTCCTGCTGAA[G/T]AAATCTTTGCCTACT | 257397 |
rs771892772 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828211 | TACCTCTTAAAAGAC[C/T]ATATAAAATTGAATT | 257397 |
rs771964056 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30867322 | CTAATTGTAACAAAC[A/G]TACCATGCTAATGTA | 257397 |
rs772013995 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30888713 | CTCAACGGCCCCCAC[A/G]CTGGTGCTGCTAGTC | 257397 |
rs772085645 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884735 | TATCCCTCACTTAAT[C/T]GTCTGAACATCACAA | 257397 |
rs772126840 | snp | A/G | 2.28003e-05 | 0.00337634 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855113 | CCGAGGTATGTGCAT[A/G]TATGAAGGAGGTGGC | 257397 |
rs772139180 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829439 | GACCATCACTAAAGA[A/G]ATATGAAACCATACA | 257397 |
rs772155070 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852649 | TCATCTGTTGTTTTT[A/T]AAAAAAGCAACAATA | 257397 |
rs772158208 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30886672 | TAGAACTTTCAGCCA[A/G]AGATAATTAACTAGG | 257397 |
rs772166985 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876800 | AACTAAGAATTCAAT[A/G]AACAGGTCTAACAGC | 257397 |
rs772202267 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863117 | CTGACTTTTCACAAC[A/C]AATAGGAATCTAAAC | 257397 |
rs772208061 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30857577 | TCTCTACACTGAGTT[A/T]GCCTACTTAGTATTG | 257397 |
rs772254817 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848512 | GAGCAACAGAGTGAG[A/G]CTCTGTCTCAGAAAC | 257397 |
rs772302933 | snp | A/C | 2.44834e-05 | 0.00349873 | missense, intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834057 | AGTACAAACCATCTG[A/C]AGCTGCTGCCTGGGT | 257397 |
rs772315477 | snp | A/G/T | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831318 | TTCCTCCTCCCCGCT[A/G/T]TGCAATCGAAAATGA | 257397 |
rs772317753 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887370 | GACGCATCTGAAAAG[A/G]AAAAAAAACCTTGAG | 257397 |
rs772393919 | snp | C/T | 4.84731e-05 | 0.00492282 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842921 | GAAATCCCAAATTAT[C/T]TTGACATTTATTTCT | 257397 |
rs772416853 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30839388 | TTTTATATAGTGACT[A/G]TAAGTCAATGAGATA | 257397 |
rs772448728 | snp | C/G | 2.73273e-05 | 0.00369633 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854979 | TGTCTAATATAAATA[C/G]AACCAGGAGACCCAT | 257397 |
rs772450668 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862197 | TTTAATGGTAGGGAT[A/G]ACCTTAACTAATCAA | 257397 |
rs772481175 | in-del | -/AT | | | intron-variant | TAB3 | GRCh38.p7 | X:30866235 | CACCCCCCACAAAGA[-/AT]ATGTTAGCTGCCACA | 257397 |
rs772493007 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828256 | GATATGAACCCTAGA[C/T]AACTGTGACAAAGCA | 257397 |
rs772504580 | in-del | -/TA | | | intron-variant | TAB3 | GRCh38.p7 | X:30868568 | TATATATATATAGCT[-/TA]TATATATATATATAT | 257397 |
rs772511774 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30864084 | CACTTTAAAGCCAGA[C/G]AGAGGACTCAAGCAG | 257397 |
rs772585116 | in-del | -/A | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828140 | ATATTTTTAGAGGAC[-/A]AATTCTTCTATGCCT | 257397 |
rs772595673 | snp | A/G | 0.000529801 | 0.0162671 | intron-variant | TAB3 | GRCh38.p7 | X:30880713 | AGAAGTACATGACAC[A/G]TTTTTGAAGAAATTC | 257397 |
rs772596706 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30874642 | TGCTGGATGCTGAAA[A/G]CAATGATTTGAAAAT | 257397 |
rs772682765 | snp | C/T | 2.31895e-05 | 0.00340503 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854729 | GCCCAACTGGGAAGG[C/T]TGCACTTGATGCTGT | 257397 |
rs772691223 | in-del | -/T | 0.000529801 | 0.0162671 | intron-variant | TAB3 | GRCh38.p7 | X:30880714 | GAAGTACATGACACA[-/T]TTTTGAAGAAATTCC | 257397 |
rs772698160 | in-del | -/GAA | 0.00211696 | 0.0324653 | utr-variant-5-prime, cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30871778 | CACGGTCAAAAACTT[-/GAA]GAAAAGGCTGAAGAC | 257397 |
rs772704309 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30846997 | AATCAACCTGTTAAA[C/T]GAGTCATGTCCATGA | 257397 |
rs772742560 | snp | A/G | 0.0068637 | 0.0581785 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890596 | TGTCTGACAGGCATA[A/G]GATTTAGTCCAGTGA | 257397 |
rs772755123 | snp | A/G | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30881668 | GTTTTTGTTAAACAA[A/G]AGGGTTTTTACATCT | 257397 |
rs772759775 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30866788 | TTCACCTCAAGGAGG[A/T]GGAGCATAACCTCCC | 257397 |
rs772867499 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878860 | CTTTTAAAAAACCCA[C/T]GGATCAAAAAAGAAA | 257397 |
rs772881059 | snp | A/G | 2.37026e-05 | 0.00344249 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855396 | CCACCATTAAGTTGG[A/G]CTCCATCTCCTGGGT | 257397 |
rs772906310 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888794 | ACTCTCCGCAATGCC[C/T]AGGGTCCGGCGAGGA | 257397 |
rs772910195 | in-del | -/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843087 | GGCATTTAAGAACTC[-/T]TTTTTTCCTGTTATT | 257397 |
rs772950043 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30870441 | AGCTTGGCGATACAG[A/C]AGACCCATGTCCTCG | 257397 |
rs772958815 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30870186 | TCTGTGTGATTTCTC[C/T]CAAGTGCAGCCTAGA | 257397 |
rs773002455 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829765 | TATGATGAGTTATTA[C/T]GCCTTTGGTTTCATT | 257397 |
rs773054937 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30887573 | TCTAGCTCTGCAATT[C/T]ACCAGCTATATAATC | 257397 |
rs773060852 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851084 | TGGAGAAAATGAGGC[A/C]GAAATTTGATTTATA | 257397 |
rs773088580 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30849112 | TTGTTACCATTTAGC[G/T]GGTCAACACTTCTGA | 257397 |
rs773130278 | snp | C/T | 2.28001e-05 | 0.00337632 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854443 | CTCTTGAAGGAGAAC[C/T]TGAAGGTGGCGTGGT | 257397 |
rs773136120 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884760 | TCACAAACAGTGGTA[A/G]CAGTATGTAACCTCA | 257397 |
rs773141644 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829966 | TTATTGCTGTTTATA[C/G]TCACCAAAATGAGGG | 257397 |
rs773159405 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30874854 | AGTGCCAAGAAAGAC[A/G]GTAAATGAACTGGAA | 257397 |
rs773191592 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852675 | CAATAACAACAACAA[A/C]AAAAAACCGGAACTC | 257397 |
rs773235194 | snp | C/G | 9.26323e-05 | 0.00680496 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854184 | TGGCTTCCCTTTTCT[C/G]CCCCAGAGCCTGGTA | 257397 |
rs773248865 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30886243 | GATATGAGGCAATTT[C/T]CTGGTGTTTTATCTT | 257397 |
rs773255177 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30839624 | AATATAAGTTCATCA[A/G]TTGTTACAAACGTAC | 257397 |
rs773265322 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30842427 | GTTATAGTTTTTACA[A/T]TGCTAAGTAAATTTA | 257397 |
rs773267296 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30833171 | GAGACAGGGTTTCAC[C/T]GTGTTAGCCAGGATG | 257397 |
rs773278587 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30876280 | ACTATCATCCTTGGT[G/T]TCAAATGATTTTTCA | 257397 |
rs773320318 | snp | A/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30841737 | ATGATCAATCTACCT[A/T]GAGTTGCTTAAGGCA | 257397 |
rs773320621 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30868235 | ACAAAGTGTGTATAA[C/G]TTTTTGAAAAATGCT | 257397 |
rs773398886 | snp | A/G | 2.28875e-05 | 0.00338278 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854677 | GTTGATATGGATGGG[A/G]TGGAGTAGTTGAAGG | 257397 |
rs773411912 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835287 | CAGAATCCAAAGCAT[G/T]GTGCTCAGGTACTTA | 257397 |
rs773436228 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876870 | GGGGGAAAATAAAAC[A/G]CTCAGAATGAAGAGA | 257397 |
rs773439991 | in-del | -/GCT | 0.125056 | 0.216539 | intron-variant | TAB3 | GRCh38.p7 | X:30868548 | TAGCTTATATATATA[-/GCT]TATATATATATATAT | 257397 |
rs773505510 | in-del | -/GC | | | intron-variant | TAB3 | GRCh38.p7 | X:30868618 | AGAGAGAGAGAGAGA[-/GC]GCGTGGGGGGGAGAG | 257397 |
rs773536584 | snp | C/T | 2.54304e-05 | 0.00356575 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855553 | AACAGGCTTCAAGAT[C/T]GTTGTTATTCTAGGG | 257397 |
rs773595753 | in-del | -/AGAT | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30848562 | CAGGCTCATTTCCAA[-/AGAT]AGATAGTAGAACCAC | 257397 |
rs773613673 | in-del | -/CCT | | | intron-variant | TAB3 | GRCh38.p7 | X:30849014 | AAACTTAAATTTCCC[-/CCT]CCTCCTTGAAACTGT | 257397 |
rs773626684 | snp | A/C | 5.056e-05 | 0.00502767 | intron-variant, missense, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846010 | ACAGAAAATGAAGAC[A/C]ATCTCTAATCTGGTG | 257397 |
rs773639711 | snp | C/T | 0.00370173 | 0.0428621 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830686 | AATGCATCTCTTATG[C/T]GGCATAAGTAGGTCT | 257397 |
rs773654835 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874664 | TTTGAAAATGAGATA[C/T]GAGGGCGGTTCAGAA | 257397 |
rs773702361 | snp | G/T | | | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845471 | GATAATATTTTAGAC[G/T]TTGTGGACCTGTGAT | 257397 |
rs773705550 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852050 | TAGCATAGTACCACA[C/T]TGCATAAACTATACG | 257397 |
rs773727956 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828339 | AATTGAGACCAGCTC[C/T]TTAAAAATTAAACTG | 257397 |
rs773752943 | in-del | -/CTA | 2.37423e-05 | 0.00344537 | cds-indel, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855417 | TCTCCTGGGTGATAG[-/CTA]CTAGGAGAATGGATA | 257397 |
rs773753738 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30847147 | GAGGAAACTGAGGCA[C/G]AGAGAGGTTATATAA | 257397 |
rs773784403 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863190 | TAATAGTGGTTAGCA[A/C]TCTGCCCTGTACAAA | 257397 |
rs773814121 | in-del | -/TTTG | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30840189 | TTGAAGTTTATTGAT[-/TTTG]TTTATCTTTTCAAAG | 257397 |
rs773817632 | snp | A/G | 8.13262e-05 | 0.00637624 | intron-variant | TAB3 | GRCh38.p7 | X:30855597 | AAAGTAACATTGGCA[A/G]CATTAACAAATTCTA | 257397 |
rs773891230 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830869 | TGTGTGTTGGAAATT[A/G]CCCCTGAAAAAAGCA | 257397 |
rs773901517 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30867918 | GAAGCATGCATATAA[-/T]TTTTTTTTTTTTTTT | 257397 |
rs773909690 | snp | C/T | 8.74508e-05 | 0.00661194 | intron-variant, stop-gained, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846084 | CTTCTGTAAAAAAAT[C/T]CAAAAAACTAAAACT | 257397 |
rs773909855 | snp | A/G | 0.000569199 | 0.0168605 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855440 | AGAATGGATACCCAG[A/G]TTAATATGTAAAAGG | 257397 |
rs773911041 | snp | C/G | 0.00105904 | 0.0229869 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30871797 | AAAAGGCTGAAGACA[C/G]TGTCCTGAAAAATAA | 257397 |
rs774017528 | snp | G/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829802 | TTAAGAGCAGCTTGT[G/T]TTTCCAGGTCTGCCA | 257397 |
rs774047114 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30865604 | TAATATTATCATCCA[C/T]GTTTTACAAATAAGG | 257397 |
rs774100808 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30878306 | GACCAGTCTGGTCAA[C/T]ATGGTGAAACCCCGT | 257397 |
rs774101684 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841066 | GCATATGATGCTGCC[-/A]AAAGTGCCAAATCTG | 257397 |
rs774102029 | snp | G/T | 2.30285e-05 | 0.00339319 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854190 | CCCTTTTCTCCCCCA[G/T]AGCCTGGTATCACTG | 257397 |
rs774105023 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30833115 | AGCTGGGACTACAGG[C/T]GCCTGCCACCGCACC | 257397 |
rs774134984 | snp | A/T | 0.00211696 | 0.0324653 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836427 | GCATCTATCTACATA[A/T]TTGAGCTACGCATTG | 257397 |
rs774151075 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30885904 | GAGGAGTTTTGGTGC[C/G]TTCCTTGTTAGCATC | 257397 |
rs774155609 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30889045 | AGGCACAGGGTCACT[A/G]GGACGATCCCGGGGG | 257397 |
rs774190297 | snp | C/G | 2.28511e-05 | 0.0033801 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854332 | TTGGTATCACTCGAG[C/G]AGATGGTGATGGAGT | 257397 |
rs774204144 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30887284 | TTTCAGATAGGTCAC[C/T]ACCAGCTATCAGGAA | 257397 |
rs774222073 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30873129 | CCAACTATCAAAAAA[C/G]GAATTTTTTTTAGAC | 257397 |
rs774271345 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862047 | AATAATAGGCGACTA[C/G]CTACAACTCTTAGAT | 257397 |
rs774293657 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885675 | GGATGAGTGTACAGT[C/G]CCTGTTCCTGCAGCA | 257397 |
rs774377032 | in-del | -/AATT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850342 | TTTATGTATCTTTGA[-/AATT]AATTATAATAAAAGT | 257397 |
rs774386553 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829849 | TAGAAGTGGGGGGGC[A/G]GTGTAGGGGGGTTGG | 257397 |
rs774453168 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875020 | CCAGAGCTGGTGGTA[A/C]CATGTTCTAGAAATG | 257397 |
rs774498419 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843531 | GCCAAATATAAACAT[G/T]TACAAGGATTAATCA | 257397 |
rs774526106 | in-del | -/AA | 0.00317376 | 0.039709 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831247 | GAGTTAAGAAAGGAG[-/AA]AAAAAAGACCTCCCC | 257397 |
rs774542649 | snp | A/G | 3.29679e-05 | 0.00405991 | stop-gained, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854956 | TTCCTGATGAACTCT[A/G]AGATGTCTGTCTAAT | 257397 |
rs774556412 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30864802 | TGTGTGTGTGTGTGT[-/T]GTTTTTTTTTTAAAG | 257397 |
rs774577458 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830582 | CAAAGCGCAGTTTTA[C/T]GAGAATATCATTTAT | 257397 |
rs774620446 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30853054 | GGGGGTTGGCATTTA[C/T]TCTCATGTCTTTCTA | 257397 |
rs774634714 | snp | A/G | 7.42721e-05 | 0.00609348 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30831520 | CCATGGAGCCCCTTC[A/G]TAGTCTTCATCTCGA | 257397 |
rs774642032 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30855733 | AAAAGGAGACCCAAA[C/T]GATTCATATTATTTT | 257397 |
rs774679271 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30871092 | TAGAAAGATAAACTA[C/T]GTAGAAATCACGGCT | 257397 |
rs774720430 | snp | C/G | 7.77726e-05 | 0.0062354 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834034 | TCTGCACAAACTCTG[C/G]ACACACAAGTACAAA | 257397 |
rs774722542 | snp | A/G | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836437 | ACATAATTGAGCTAC[A/G]CATTGAGCATTCAAT | 257397 |
rs774756426 | snp | C/G | 2.37942e-05 | 0.00344914 | intron-variant | TAB3 | GRCh38.p7 | X:30846660 | CTAGTAAGAAAGGAC[C/G]CAAAATAGCAATTGT | 257397 |
rs774778845 | in-del | -/G | 2.29297e-05 | 0.0033859 | frameshift-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854687 | TGGGGTGGAGTAGTT[-/G]GAAGGACTAGGTGGC | 257397 |
rs774797388 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30855965 | GTAATATCCATTATT[-/A]ATATTTAAATTGATA | 257397 |
rs774841065 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30859881 | CAGAAACACTAAACA[C/T]GCTATACTGAAACCA | 257397 |
rs774858866 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863063 | GAAGCCAACAGCTTA[C/T]AAAAATGGCTACCAT | 257397 |
rs774868621 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845323 | CTTGTATATAGCTAT[A/G]TTTTAAAGTTAGTTA | 257397 |
rs774881072 | in-del | -/AT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30860986 | TGTGTACATACAAAC[-/AT]GTGTACATGCACACA | 257397 |
rs774920069 | snp | A/G | 2.34541e-05 | 0.0034244 | intron-variant | TAB3 | GRCh38.p7 | X:30852735 | ATGACCTGACAGCCA[A/G]TATCCCGACCCTCCT | 257397 |
rs774934008 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870182 | AATTTCTGTGTGATT[G/T]CTCTCAAGTGCAGCC | 257397 |
rs774978707 | snp | A/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885475 | CCCTCCCATAACTGG[A/T]AGTCTGAGCTTCCCT | 257397 |
rs775022911 | snp | C/T | 4.58568e-05 | 0.00478814 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854686 | GATGGGGTGGAGTAG[C/T]TGAAGGACTAGGTGG | 257397 |
rs775036258 | snp | A/G | 9.58359e-05 | 0.00692162 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846116 | TGATTATAGTTGAAT[A/G]TTTTCACATAACATA | 257397 |
rs775112698 | snp | C/T | 3.30743e-05 | 0.00406645 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859613 | AATGGTGGCCAAGTT[C/T]CTCTTAGGAAATGGA | 257397 |
rs775113718 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30832257 | AATGCCCATACCTGG[A/C]AACCTTATGTTGGTC | 257397 |
rs775116166 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30864545 | AGAGAGGAAGCTCCC[C/G]CAGAGCTCTGCTCTA | 257397 |
rs775124764 | snp | C/T | 9.13795e-05 | 0.0067588 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854632 | AGGCTACTGAATGGC[C/T]TCCCTGTTTCTGATA | 257397 |
rs775224898 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848702 | TCAAAAGTAGTTTTC[A/G]TGCAGGAGGAATTTC | 257397 |
rs775285238 | snp | G/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828618 | TGTACTTTAACAAAA[G/T]GGCAAACGTGCTTTC | 257397 |
rs775298128 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844229 | ATTCGTTATGAAAAG[A/C]GATTTAGAAATGCCT | 257397 |
rs775339710 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835118 | CTAGAAAATTGTTTC[C/T]ATAAATTTATAGTTT | 257397 |
rs775343532 | snp | A/G | 0.00105904 | 0.0229869 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891082 | GCTCCAGTGTCAAGA[A/G]CCACTCATTTTGGAA | 257397 |
rs775361358 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30882186 | AGACTGGATTGTTGC[C/G]ACAAATCGAAACCAA | 257397 |
rs775403939 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30868006 | GGCTCAAGTGATCCT[C/G]CCATCTCAGCTGCCC | 257397 |
rs775411710 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30852550 | TACCTTGATTATAAT[C/T]GTCAGTGTTTGAAAA | 257397 |
rs775418714 | in-del | -/C | | | intron-variant | TAB3 | GRCh38.p7 | X:30882593 | TCCCTAGAGGAAACA[-/C]CTAGCCTTCGAGTAT | 257397 |
rs775452169 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30891116 | GGATGTGGTCAGAAA[A/G]GGGGTCATTCACTCC | 257397 |
rs775611159 | snp | A/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889820 | CTTCTAACCCTTTGC[A/T]TGTCCTTATGGGTTT | 257397 |
rs775624507 | in-del | -/TA | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30868481 | CTTATATATATAGCT[-/TA]TATATATATATATAG | 257397 |
rs775631130 | in-del | -/TTG | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30851129 | CCATTAAAGATAACT[-/TTG]TTATTTTCCAGTGCT | 257397 |
rs775654423 | in-del | -/A | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829522 | AGAGACCAGTGTTAC[-/A]AAAACCTTTGAAGAA | 257397 |
rs775691680 | snp | C/T | 4.74271e-05 | 0.00486942 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834077 | GCTGCCTGGGTGTCA[C/T]GGATGTCTGCCTGTA | 257397 |
rs775711914 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878428 | TTGCTTGAATCTGGG[A/T]GGCAGGGGTTGCAAT | 257397 |
rs775736789 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30870976 | GCCAAGATTATTAAA[C/T]GGGTGTCACAACATC | 257397 |
rs775740206 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853400 | TTTTTAGCTAATCCA[A/G]TAATTCCACTTCTTA | 257397 |
rs775745087 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838108 | TGGTTAGTCTAAGAC[A/T]TTTTTTTCCTTTTTG | 257397 |
rs775757884 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30860892 | AATATTCCTATTTTT[C/T]GGTATTAGACAATGA | 257397 |
rs775780748 | snp | C/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830524 | ATTTCCAAATGGATT[C/T]TGGAATGGACTTGCA | 257397 |
rs775806568 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30874338 | ATTGTAGCTATGTAA[A/G]AAAATGTGTTGTTTT | 257397 |
rs775812562 | in-del | -/AGG | 2.33146e-05 | 0.0034142 | cds-indel, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846562 | ATACCTCTAGATTGA[-/AGG]AGGTCAACTTCTTTC | 257397 |
rs775824330 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30879128 | AATAGAAACACTTGA[A/C]GAATACTATTAGTAT | 257397 |
rs775841451 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30833072 | GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 257397 |
rs775895820 | snp | C/T | 9.11962e-05 | 0.00675202 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855125 | CATGTATGAAGGAGG[C/T]GGCGGTGGTGGTGAA | 257397 |
rs775994461 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888915 | TCTGGGGCGGGCGCG[C/G]ACGCGCCAGGCCCTG | 257397 |
rs776011680 | snp | C/G | 2.72339e-05 | 0.00369001 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854982 | CTAATATAAATAGAA[C/G]CAGGAGACCCATAGA | 257397 |
rs776024228 | snp | A/G | 2.68868e-05 | 0.00366642 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859560 | TCATGGAGAACCTGA[A/G]TATCAAGCTGTGGGC | 257397 |
rs776082504 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30846917 | CATACAAGATACTAC[C/T]GTTTTAATCATAGAG | 257397 |
rs776099611 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828302 | GAAACATTGATTTAT[C/T]TGCATAATTAAAAAG | 257397 |
rs776110597 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30871982 | AGAAAGTTTTCCTGA[C/T]TGCCTGAGCCAGCCT | 257397 |
rs776125129 | snp | A/G | 0.00158814 | 0.0281345 | intron-variant, missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836830 | CCTGGGCGACAGAGC[A/G]GGACCCTGTCTCAAA | 257397 |
rs776130541 | snp | C/T | 2.28425e-05 | 0.00337946 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854214 | ATCACTGAAATGGGC[C/T]GAATAGGTTCTGGTG | 257397 |
rs776137921 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30848157 | TTTAGGGAGTTGGGG[A/G]CAAGAGAGATGTTTC | 257397 |
rs776163562 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30882121 | GCATGTGTGAAAAGT[C/T]AGAGTAACAATGGCA | 257397 |
rs776178625 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845797 | CTTTCATAGAAAGAG[C/T]GGCTTTCTCCTTCAT | 257397 |
rs776230262 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30857449 | ATTCTTTTTTTTTTT[A/T]TAGACCTATGGATTA | 257397 |
rs776251461 | in-del | -/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30840267 | TTTCCTTTCTTCTAC[-/T]TTTGTTTTTACTTTG | 257397 |
rs776302782 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30848647 | TCTGATTAAACTGAG[C/G]GGGGAAAAAAAGCAG | 257397 |
rs776305658 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30860051 | GTCAACTTGAAGAGG[G/T]GCACTCACTGGCCAC | 257397 |
rs776359949 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30862548 | AGAGATCTTGAGAGC[A/G]GCCAGCTCTCACCTA | 257397 |
rs776371447 | snp | C/G | 3.33751e-05 | 0.0040849 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859638 | AATGGATGTTAACCG[C/G]CTTTCCAAAAGTAAT | 257397 |
rs776394183 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30851962 | CGTGAACATATACAG[C/T]ACTTACCACACTGTA | 257397 |
rs776440700 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30851909 | AAGTGCAATGAATCT[A/G]CACAGAAACGAGTTG | 257397 |
rs776480671 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843205 | GTCCTCCCAATGAAA[C/T]TGTGTTTTCATCGCT | 257397 |
rs776485344 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30870223 | CATGTAGCATCCTCA[C/T]GTACCTATAGGAGGC | 257397 |
rs776493352 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30866920 | AAACCTGACAAACAC[A/G]TTCTCAGCCAGGTGA | 257397 |
rs776500914 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30831811 | ATGGATATATGTCCA[C/G]AATAGATTGCCTTCC | 257397 |
rs776526799 | in-del | -/ATG | | | intron-variant | TAB3 | GRCh38.p7 | X:30882283 | AAATCAATCATAACT[-/ATG]ATGAGTACTAAAAAA | 257397 |
rs776541162 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30850985 | TAAAGGTTTCCAAAG[C/T]ACCCAACTACTACGG | 257397 |
rs776658578 | in-del | -/GC | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30868565 | ATATATATATATATA[-/GC]TTATATATATATATA | 257397 |
rs776679250 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30857819 | ATAAGGATAAAAAAT[A/G]TATCAAACAGTAAAC | 257397 |
rs776740419 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30841080 | CCAAAGTGCCAAATC[C/T]GGCACTCGGCAGTCA | 257397 |
rs776741348 | snp | C/G | 2.33842e-05 | 0.00341929 | intron-variant | TAB3 | GRCh38.p7 | X:30852745 | AGCCAATATCCCGAC[C/G]CTCCTATTAACACAT | 257397 |
rs776771790 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30858775 | ACAGGGAAAGTGGTA[A/G]GCCAACTTCTCTGTT | 257397 |
rs776826370 | snp | C/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828250 | AGGTTGGATATGAAC[C/G]CTAGACAACTGTGAC | 257397 |
rs776850721 | snp | A/G | 0.0505727 | 0.150761 | intron-variant | TAB3 | GRCh38.p7 | X:30859394 | CACACACACACACAA[A/G]AAAACATACCTGGGT | 257397 |
rs776882559 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30876752 | TTAAAAGAAGCAAAG[A/G]ATAATTTTATTACTG | 257397 |
rs776900252 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869348 | TACAGGTGTGAGCCA[A/C]TGCGCCCAGCCTTTT | 257397 |
rs776936160 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889580 | GAAGTTACTGCGCCT[A/G]CGTGCGCGGGTAATG | 257397 |
rs776941044 | snp | C/T | 2.28133e-05 | 0.0033773 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854397 | TACACAGGATTAACA[C/T]TAAATGGAGGTTTTG | 257397 |
rs776945536 | snp | C/G | 2.27993e-05 | 0.00337626 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855130 | ATGAAGGAGGTGGCG[C/G]TGGTGGTGAAGGCCC | 257397 |
rs777033528 | snp | A/G | 2.34066e-05 | 0.00342093 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855353 | AGGATCAATATGTCC[A/G]TCACTTGAGCTATGT | 257397 |
rs777072092 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30877033 | AAACCACATGTGTAA[C/G]AATCTCAATGAATTC | 257397 |
rs777080372 | in-del | -/TATT | | | intron-variant | TAB3 | GRCh38.p7 | X:30850324 | GGGGGTTCATTATAC[-/TATT]TATTTTATGTATCTT | 257397 |
rs777116102 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30863315 | TCATGTTAAAATACT[C/T]TAAAAAAGCAACTTC | 257397 |
rs777129694 | snp | C/T | 2.28423e-05 | 0.00337944 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854308 | TAATTTTAAAAACTG[C/T]AGTTGGGTTTGGTAT | 257397 |
rs777130832 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878365 | ATTAGCCAGGTGTGG[A/T]GGCACGTGCCTGTAG | 257397 |
rs777152224 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852366 | ATTGATCTAACTCAT[C/G]TGAATTAATGTACTT | 257397 |
rs777193769 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829675 | GACTAGTGGATATAT[C/T]TTGGGGAGTTTTTCA | 257397 |
rs777200208 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30887712 | TAATCGACGTTAGCT[C/G]TGTTTGCTCCAACAA | 257397 |
rs777218318 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853336 | CTATTAGCTAATCCA[A/G]TAATCTACTATTAGC | 257397 |
rs777340978 | snp | C/G | 0.00146772 | 0.0270501 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852854 | ATACCATTAACTTCA[C/G]ACTTCAACCGCTCTA | 257397 |
rs777347188 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30864387 | GGGCCCAGATGCTAT[A/G]CTTAGCAGTGGAATC | 257397 |
rs777351339 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30857331 | GCAAGGAAGGGAAGA[C/T]ATTAAAAACAAATTT | 257397 |
rs777429768 | snp | A/T | 0.00633741 | 0.0559334 | intron-variant | TAB3 | GRCh38.p7 | X:30868408 | ATATATATATAGCTT[A/T]TATATATATAGCTTA | 257397 |
rs777441848 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838675 | GGTATATCACTCCAT[C/T]TACTTAGGTCTTCTT | 257397 |
rs777454256 | snp | A/T | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30860344 | AAAATCTGGATGAAG[A/T]GTAGGAAATACACAC | 257397 |
rs777485137 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30842265 | GGGAAAATACCTAGT[C/T]GCTACCAATTGCTAT | 257397 |
rs777533100 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834781 | GCATGCCACTACCAC[A/G]CCCAGCTAATTTTTT | 257397 |
rs777548931 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876270 | TTTCTGAAAAACTAT[C/T]ATCCTTGGTTTCAAA | 257397 |
rs777560603 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30862598 | AAACCTCAGATGCTA[A/C]TGAATCCAAGGTTAC | 257397 |
rs777566499 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870656 | TAAAGCTGGAAGAAA[C/T]TCCACATCATCTAAC | 257397 |
rs777577516 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30839757 | AGAAATACGGGAAGC[A/G]TTCCCTCCTGTATTT | 257397 |
rs777629887 | in-del | -/TTAT | 2.69691e-05 | 0.00367203 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846521 | ATACCACACTATTAC[-/TTAT]GGTTTACCAAATAAT | 257397 |
rs777663669 | snp | C/T | 0.000102847 | 0.00717029 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30834203 | CCAGTCTTTCAACTG[C/T]AAGAGTGAACAGGCT | 257397 |
rs777700072 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890445 | GATTAGTTTTGGTAG[A/G]GACAGGGTTTCTCCT | 257397 |
rs777737140 | snp | A/C | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830983 | GCAATGGGAAGAAGC[A/C]CGGGGAGCCTTGGTT | 257397 |
rs777745056 | snp | G/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30844655 | CCTACATCATGCATA[G/T]TAATTCTTTGATTGC | 257397 |
rs777860992 | snp | A/G | 0.000432444 | 0.0146981 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854922 | GAGGACTGCCACGGC[A/G]TACTCTGAGGAGTTT | 257397 |
rs777865608 | in-del | -/T/TTT | 0.179082 | 0.239885 | intron-variant | TAB3 | GRCh38.p7 | X:30832973 | CATTTTCTTTCTTTC[-/T/TTT]TTTTTTTTTTTTTTT | 257397 |
rs777883282 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30878201 | GGGCAAATATTAAGA[C/T]ACCTCTTGGCTGGGT | 257397 |
rs777921813 | in-del | -/C | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30841414 | AGAGAGTCTCCATCT[-/C]AAAAAAAAAAAAGAA | 257397 |
rs777930809 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30877889 | CCATCTAAAACATAA[A/G]AATACAGAAAGGTTA | 257397 |
rs777963703 | snp | A/C | 0.000529661 | 0.016265 | downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827295 | TAATGTGCACTTAAT[A/C]CCCCAAATCTAACAT | 257397 |
rs777983614 | in-del | -/A | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888466 | CCTCACCTGTCCCTC[-/A]ACCCTTCAAATCCTG | 257397 |
rs778022640 | snp | A/G | 0.00633741 | 0.0559334 | intron-variant | TAB3 | GRCh38.p7 | X:30873488 | GGAGATCGCGCCACA[A/G]CACTCCCGCCTGGGC | 257397 |
rs778065500 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30830460 | ATTGGAAGGAAAAAA[A/G]AAAGGCCCTATGGAC | 257397 |
rs778093383 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30853262 | AAAACTAAATTCTCC[A/G]GTTATCTTGAAACAA | 257397 |
rs778095002 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869009 | TAAATGCTGTTTCTA[C/T]CATGTGTAATACTTT | 257397 |
rs778134080 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30840960 | TTAGTAGACATTCAG[A/G]CAAAATCGAGTTTAA | 257397 |
rs778143843 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30858331 | TGGTTTCACTCCGGT[A/G]GGAAGTGTCTTTGCT | 257397 |
rs778245990 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30850015 | CCTAAGAAAAATCCC[A/G]TAAGATGAGTACTAT | 257397 |
rs778298928 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30849149 | GCCTTATATTTTCTC[C/T]CTCACACAAATACAT | 257397 |
rs778322101 | snp | C/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30861403 | TCAGGGGAGTGGAGT[C/G]ACCTATATAGGGCAA | 257397 |
rs778324196 | snp | A/G | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890247 | TGGGGGGAGGATATA[A/G]AATACATCAAAGAGG | 257397 |
rs778337453 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30835905 | TTTATTCGAACCAAT[A/C]AACCTATTCTACCAG | 257397 |
rs778342161 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854881 | GTAAAGGACGCTGGC[C/T]ATAGTGAGGCACTGG | 257397 |
rs778364962 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30858029 | ACATTTTAATGTGAA[-/T]TAAAGCAGTTTTCCA | 257397 |
rs778376258 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30848384 | AAAATTAGCTGGGCG[C/T]GGTGGTGCGTGCCTG | 257397 |
rs778429369 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30849690 | ATATAGCCAGTGAGC[A/G]CCTGAGCAATTCTGA | 257397 |
rs778430058 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869787 | CTTAGAACAGTGTTT[C/T]TCAAATGGTGGGTTT | 257397 |
rs778437532 | snp | A/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829539 | AAACCTTTGAAGAAC[A/G]TTGTTTTGGGGACCA | 257397 |
rs778448391 | in-del | -/TAA | 0.000529661 | 0.016265 | utr-variant-3-prime, cds-indel | TAB3 | GRCh38.p7 | X:30830247 | TATTCACCTTTCTCT[-/TAA]TAATTTTTGACAATC | 257397 |
rs778466682 | snp | A/G | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30866651 | ATTATGATCCAACGT[A/G]TAAAATAAATAGCCA | 257397 |
rs778485171 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30850245 | GGAAACACTTAAATG[C/T]CTTATCTCTCAGATG | 257397 |
rs778486848 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30871353 | CTTTCAATCTCCACC[A/T]GCTCCAGTGCTGGGG | 257397 |
rs778523078 | snp | C/T | 0.000123977 | 0.00787231 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831410 | TCACTTTCAACCTGG[C/T]GCAGACTTTTCTGAA | 257397 |
rs778538147 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30851625 | GAGAATTCACAGATC[C/G]CCTTTGAAGCCAAGA | 257397 |
rs778559665 | in-del | -/ACAG | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30875235 | AATGCTGTAATATTA[-/ACAG]ACAAAGAACATATGC | 257397 |
rs778575276 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30846713 | ACATTTAAGAACTGC[A/G]TTTCATGTTAATTGT | 257397 |
rs778595174 | snp | A/C | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30874618 | ATTACAAGTGAGTAG[A/C]AAGGATGTTGCTGGA | 257397 |
rs778601156 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30850917 | TAAATAAAATGTATA[C/T]GATTAAAGAAAATTA | 257397 |
rs778626270 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30837657 | TTTTCATTTTCTTAA[C/T]AGTGTCACTTGATGA | 257397 |
rs778631789 | snp | A/G | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846406 | ATCTGATCCATGACC[A/G]TGGGACAGGGGGATC | 257397 |
rs778656540 | in-del | -/AGTT | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30878805 | ATACAAAAAATACAC[-/AGTT]AGAAAATTCTCATAT | 257397 |
rs778661957 | snp | C/G | 6.52231e-05 | 0.00571028 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30859601 | CATGCCAGAGCAAAT[C/G]GTGGCCAAGTTTCTC | 257397 |
rs778677097 | in-del | -/GAAAT | | | intron-variant | TAB3 | GRCh38.p7 | X:30839719 | CAGTAACATGAAAAG[-/GAAAT]GAAATGAAAAAACAA | 257397 |
rs778684464 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30886264 | GTTTTATCTTTATAC[A/G]GTGGCAATATAAATC | 257397 |
rs778719168 | snp | A/T | 0.00105904 | 0.0229869 | | | GRCh38.p7 | X:30847318 | AAACAAATGAATTCC[A/T]TTTGTTCCCCAACTT | 257397 |
rs778754369 | in-del | -/AAC | 0.000529661 | 0.016265 | | | GRCh38.p7 | X:30842188 | AAATCATTTTTATGT[-/AAC]AACTATCCAAAAATG | 257397 |
rs778784300 | in-del | -/TTTAAGAACTCTTTTTTCCTGTTATTTGATTT | 9.15039e-05 | 0.0067634 | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30843076 | TAAATTCATCAGGCA[lengthTooLong]TTTAAGAACTCTTTT | 257397 |
rs778791452 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30838566 | AAATGCACTACCACC[C/T]AATGGGGTTATAATT | 257397 |
rs778828455 | snp | C/T | 2.2804e-05 | 0.00337661 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854571 | ACTGTAATTTCTATC[C/T]TCTTCATGGAACCTT | 257397 |
rs778912949 | snp | C/G | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828017 | ACAGATAGATATACA[C/G]ACACACACGGTAACA | 257397 |
rs778941589 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30864135 | GGCTCAGGCATGACC[A/G]AACTCCTGGGACACC | 257397 |
rs778950464 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30840946 | CTGGCGATACTTCTT[C/T]AGTAGACATTCAGGC | 257397 |
rs779003843 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30842044 | GAACTCCTGGCCTCA[C/T]GTGATCCATCCGTCT | 257397 |
rs779051333 | in-del | -/GTCA | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30852551 | ACCTTGATTATAATC[-/GTCA]GTGTTTGAAAATACT | 257397 |
rs779052009 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30849020 | AAATTTCCCCCTCCT[C/T]CTTGAAACTGTTCCA | 257397 |
rs779106879 | snp | C/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834722 | ATCTCCTGGGCTCAA[C/G]TGATCCTCCTGCCTC | 257397 |
rs779119559 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30848285 | TCCCGGCACTTTGGG[A/G]GGCCAAGGCAGGTGG | 257397 |
rs779140786 | in-del | -/TTGTC | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30839986 | CTAATATTTACTGTT[-/TTGTC]TTGTTTTCAGTTTGG | 257397 |
rs779153446 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30876108 | GAAATAAGGGTGAAT[C/T]GCAATGAATCAGTTC | 257397 |
rs779161631 | snp | C/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829318 | CAAGTTAATTGCCTC[C/T]ACTTCAGCATATCAC | 257397 |
rs779191920 | snp | A/G | 2.28003e-05 | 0.00337634 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855095 | AATTGGATTTGTACT[A/G]TACCGAGGTATGTGC | 257397 |
rs779270267 | snp | A/G | 0.0157677 | 0.0873799 | utr-variant-5-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30867493 | ATCAACCCTGGCACA[A/G]AAATTTTATTCACAT | 257397 |
rs779305595 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30846908 | GTGTTCTACCATACA[A/G]GATACTACCGTTTTA | 257397 |
rs779315441 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30837796 | TTCTGGAAGCTTTAT[A/G]GTTTAACTTTTATAC | 257397 |
rs779347593 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833825 | TAAAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 257397 |
rs779383034 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858316 | AGCTTCATCCTTATT[A/T]GGTTTCACTCCGGTG | 257397 |
rs779391806 | snp | C/T | 0.00105904 | 0.0229869 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829068 | AAAATCAATCTGATA[C/T]CGCATACCCCACCCT | 257397 |
rs779406152 | snp | A/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30883193 | AGAGTCTGAAACCAT[A/T]CCTCAGTAGAAAGGA | 257397 |
rs779412592 | in-del | -/T | 0.00211696 | 0.0324653 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890441 | GCTGATTAGTTTTGG[-/T]TAGAGACAGGGTTTC | 257397 |
rs779445409 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30837118 | CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC | 257397 |
rs779482191 | in-del | -/TAGTT | | | intron-variant | TAB3 | GRCh38.p7 | X:30848003 | CAAGCAATATTCAAA[-/TAGTT]TAGTTTAAAATATAT | 257397 |
rs779494899 | snp | C/G | 5.25825e-05 | 0.00512723 | intron-variant | TAB3 | GRCh38.p7 | X:30831596 | GGAGGTTAGGATTAA[C/G]GGGGAGGGGGAAGGT | 257397 |
rs779499419 | in-del | -/CTGA | | | intron-variant | TAB3 | GRCh38.p7 | X:30886697 | ACTAGGCAGCTAAAC[-/CTGA]CTAAGTGACTTGGTG | 257397 |
rs779518017 | in-del | -/TT | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30881587 | AATTGATAAACTGAC[-/TT]ATATCTAGACTTAGT | 257397 |
rs779525699 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30863923 | ATATTATAGATGTGG[C/T]TACCATGCAGATCAA | 257397 |
rs779531201 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30866976 | GTCACGTTGATAGTA[C/T]GGACTGTTTGTATGA | 257397 |
rs779581070 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30865848 | TTCTTCAAGTTAAAC[A/G]GTAACAAAAAGTGGC | 257397 |
rs779586590 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30887135 | TGATAAAGCAAATTC[A/G]AACCCCTATAGATAG | 257397 |
rs779612237 | in-del | -/A | | | intron-variant | TAB3 | GRCh38.p7 | X:30856394 | AAAGGAGGTAATAGC[-/A]AACTGACACTTTTGA | 257397 |
rs779630510 | snp | A/G | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30827603 | ATCTAAAAGAGACAT[A/G]GTATTTACAAGATTT | 257397 |
rs779637884 | snp | G/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885236 | ATTTTTAAAATCATC[G/T]ATTTGAAACTCAGAC | 257397 |
rs779638035 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30888490 | AATCCTGCTTTTACG[C/T]ACTTTATGAGCTGGC | 257397 |
rs779639949 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30873669 | TCAACATGAAGATGA[A/C]AACGATGAAGACCTT | 257397 |
rs779691489 | snp | A/C | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884306 | CTCTTTTTGAGTATT[A/C]ACCATTGCTAGGCAT | 257397 |
rs779728892 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30869677 | TGGTTGCATCAATTC[A/C]TAAATGACGTTATTT | 257397 |
rs779745730 | in-del | -/A | 0 | 0 | intron-variant | TAB3 | GRCh38.p7 | X:30850848 | CTTCCAATGAAAAAC[-/A]AAAAAAAAACCAATA | 257397 |
rs779770084 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30869242 | ATTTTTGTATTTTTG[C/T]AGAGATGGGGTTTCA | 257397 |
rs779855546 | snp | G/T | 2.31626e-05 | 0.00340305 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30852894 | TCTCAAGTTTCAGTT[G/T]CTTTGCTAACCTCTC | 257397 |
rs779859066 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853148 | CTGAACATCCCTCTT[A/G]TTCTATTGTCCTAAG | 257397 |
rs779868679 | snp | C/T | 2.41397e-05 | 0.00347409 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855023 | AATTTGTGGAAGAAT[C/T]TGTAAAGCTCTTGGT | 257397 |
rs779887682 | snp | A/T | | | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30829228 | TCATGCAATAGTTTT[A/T]AAGTCATCTACATGG | 257397 |
rs779977430 | snp | A/G | 1.64738e-05 | 0.00286995 | missense, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30831440 | ATTCAGGTGTACCGT[A/G]GCATCTCGCACTGCT | 257397 |
rs780035175 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30875804 | AATGTAACCTTTCAA[C/T]TAAAAATGTATATAA | 257397 |
rs780037929 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30836391 | TGGGGTAGGAGTCAT[A/G]TTTTCCCTGTGTAAC | 257397 |
rs780051927 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30832880 | CATGACTCCAAAACA[C/T]GTAGATTTAATACAG | 257397 |
rs780060929 | snp | C/T | 2.41768e-05 | 0.00347675 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855503 | ATGGTATTCCATATA[C/T]AAGTATTTGCTACTC | 257397 |
rs780093927 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30877729 | AAAAAGAAATACAGA[A/G]CTAGTAGAATAAAAA | 257397 |
rs780132758 | in-del | -/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30839491 | TGAGGGGCAGATACA[-/T]AATGTCTTTACCAGG | 257397 |
rs780157507 | snp | C/G | 2.28144e-05 | 0.00337738 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855267 | TTGTAGTTGGGAGTA[C/G]CAGCAACAACAGCTG | 257397 |
rs780171509 | snp | C/T | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845140 | TACTGTTTGTTTAAT[C/T]TTGCCTAAAAATGGC | 257397 |
rs780195859 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30881373 | GTTTTTTTTTTAAGT[A/G]TAAAGGAGTACATTT | 257397 |
rs780212613 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30857105 | TTTTTGATACTAAAA[C/T]TCAAATACTTTAAAA | 257397 |
rs780245259 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30863558 | CCATTCACTCAAGAT[C/G]TGATTGTTTAAAACT | 257397 |
rs780263066 | snp | C/T | | | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855070 | GGAGGTTCTGGGATA[C/T]TGTAACAGTAATTGG | 257397 |
rs780296785 | snp | A/G | | | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846616 | TGGAGTTGTCTGTTC[A/G]TGCTTCTCAATCTTG | 257397 |
rs780348340 | snp | A/G | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30833270 | CACCGCACCCGGCCT[A/G]CTATGCCATTTTCAG | 257397 |
rs780365663 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30855659 | TGCAAATACTACTGT[C/T]ACAGAATAAATAGAG | 257397 |
rs780385797 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30882724 | AAAATGACTTAACAA[C/T]TCAGTGCAACATGGT | 257397 |
rs780390250 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30835192 | TTTATATTATTTGCC[C/T]TTAGGAACCAAAGAA | 257397 |
rs780392530 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30870849 | AACAGAAAATTATCC[A/G]GCCCAAGATGCCAAT | 257397 |
rs780424091 | in-del | -/ATA | 0.151636 | 0.229836 | intron-variant | TAB3 | GRCh38.p7 | X:30839916 | ATACATATATATATT[-/ATA]TATATATATATATAT | 257397 |
rs780443528 | snp | C/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30865397 | TAATTTTTCTGGTTG[C/G]TCTGGTCCAGTAATA | 257397 |
rs780473358 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30839081 | TTGCCTTGTTCCCAA[C/T]GTTGGTAAGTTCAGA | 257397 |
rs780473567 | snp | C/T | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30848392 | CTGGGCGTGGTGGTG[C/T]GTGCCTGTAGTCCCA | 257397 |
rs780509456 | snp | A/G | 0.000529661 | 0.016265 | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30833780 | AGCTTGCAGTGAGCC[A/G]GGATAGCGCCACTGC | 257397 |
rs780518072 | snp | A/G | 2.42412e-05 | 0.00348138 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854153 | TGATCCAGAACTAGA[A/G]CTTCTCTGATATTTA | 257397 |
rs780522995 | snp | A/T | 0.000529661 | 0.016265 | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30836011 | AACTATATGTACTTT[A/T]AGAAAACGCCGATTT | 257397 |
rs780602003 | snp | C/T | 2.28253e-05 | 0.00337819 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854276 | TAAAAGATTTTCAGT[C/T]GTTGCTCGGCCTACG | 257397 |
rs780647401 | snp | C/T | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30885128 | ACATAAATCTAATTC[C/T]GGACAGCTAAAGGTG | 257397 |
rs780671393 | snp | A/G | 0.00370173 | 0.0428621 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890391 | TGCCTCAGCCTCCCG[A/G]GTAGCTGCGACTACA | 257397 |
rs780678127 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30837905 | GATATCCAGTTCTTC[C/T]AGCTCTGCCTGTTGA | 257397 |
rs780694706 | in-del | -/TATC | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30849287 | CCATCATGCATCTTA[-/TATC]TATCTTGCACTTCTG | 257397 |
rs780718768 | snp | A/C | | | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30884749 | TTGTCTGAACATCAC[A/C]AACAGTGGTAACAGT | 257397 |
rs780747980 | in-del | -/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30858484 | GGGCTTGCAAACAAA[-/G]GAAGCACCTCTGTTA | 257397 |
rs780811796 | snp | C/T | | | intron-variant, utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30835855 | AATTACACTTGGATT[C/T]CTGGTATATATCTGT | 257397 |
rs780838387 | snp | C/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30859257 | TAGAGGCCTCGGATG[C/T]CTAGAACGTTTAGTA | 257397 |
rs780873834 | in-del | -/TA | 0.054582 | 0.155922 | intron-variant | TAB3 | GRCh38.p7 | X:30868438 | TATATATATATAGCT[-/TA]TATATATATAGCTTA | 257397 |
rs780912897 | snp | C/G | 2.35408e-05 | 0.00343072 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854172 | CTCTGATATTTATGG[C/G]TTCCCTTTTCTCCCC | 257397 |
rs780963943 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30827470 | TAGTTTATTTATTTT[G/T]CAGGAATCTTTGACT | 257397 |
rs781001543 | snp | G/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30831888 | AAATGAAGAAAAAGA[G/T]AAATGTTTTATAGCA | 257397 |
rs781002773 | snp | C/T | 6.85018e-05 | 0.00585202 | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30854290 | TCGTTGCTCGGCCTA[C/T]GGTAATTTTAAAAAC | 257397 |
rs781009343 | snp | A/G | 2.55307e-05 | 0.00357277 | missense, intron-variant, downstream-variant-500B, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30834150 | TGCAGGGGTCTGAGG[A/G]GTCTGCATAAAAATA | 257397 |
rs781020751 | snp | A/C | | | intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846209 | GATCCCTTTTTACAG[A/C]TATTTTAGATGTCTA | 257397 |
rs781033450 | snp | C/T | 0.00105904 | 0.0229869 | intron-variant | TAB3 | GRCh38.p7 | X:30868834 | GTCAACTTCATTTTA[C/T]AACCACAGTAGAGCT | 257397 |
rs781096126 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30853122 | TCTGAATGCAACCAA[A/G]GTGACATCACCTGAA | 257397 |
rs781111902 | snp | C/T | 5.78252e-05 | 0.00537673 | intron-variant | TAB3 | GRCh38.p7 | X:30831615 | GAGGGGGAAGGTAAA[C/T]AGATTAACCTTTTTC | 257397 |
rs781167128 | snp | C/T | 2.33697e-05 | 0.00341823 | missense, intron-variant, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30846559 | TCTATACCTCTAGAT[C/T]GAAGGAGGTCAACTT | 257397 |
rs781211772 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30876351 | CAATCAGGCACACGA[A/G]GAAACATAATAAGAT | 257397 |
rs781236447 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30874182 | GTCTCAAAACAACAA[C/T]AACAACAACAACAAC | 257397 |
rs781266552 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30833259 | CAGGTGTGAGCCACC[A/G]CACCCGGCCTACTAT | 257397 |
rs781280172 | snp | A/G | 9.09918e-05 | 0.00674445 | intron-variant, utr-variant-3-prime, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30845967 | CAAAAGTATGCAGCA[A/G]CTGTGGACATCAGTC | 257397 |
rs781290025 | snp | C/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30859304 | GGCCGACTCCCACAA[C/G]AGAGAATTATCCAGG | 257397 |
rs781290699 | snp | A/G | | | intron-variant | TAB3 | GRCh38.p7 | X:30875514 | GGGCAGATATATATT[A/G]TACCTACATATAAGT | 257397 |
rs781303485 | snp | A/T | 0.000529661 | 0.016265 | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30889594 | TGCGTGCGCGGGTAA[A/T]GACGCATGCCCGGAA | 257397 |
rs781326558 | snp | C/T | 0.0026455 | 0.0362733 | intron-variant | TAB3 | GRCh38.p7 | X:30879976 | TATCTACAAATAAAA[C/T]TCTCAAAAGTTGTGA | 257397 |
rs781328704 | snp | C/T | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30869937 | AAAACTTGTTTCAGG[C/T]ATGTGCGTATGTACT | 257397 |
rs781340955 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30861260 | ATCAATTTCACTATA[C/T]TAAACCAGTCTACCT | 257397 |
rs781351437 | snp | C/T | | | intron-variant, downstream-variant-500B | TAB3 | GRCh38.p7 | X:30842564 | TTTTAAAAACTAAAG[C/T]TTGGGGACATTTCAT | 257397 |
rs781365284 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30866382 | CAGCACCCAGTTCTT[C/G]ATTTCTAATTGCATT | 257397 |
rs781502983 | snp | A/T | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30888664 | TCCAACAATTCTTAC[A/T]ATACTGCTACTAACC | 257397 |
rs781516964 | snp | C/T | 0.000529661 | 0.016265 | intron-variant, upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30883994 | CTAGTTTTGCTCAAA[C/T]ATCAAAAAGGCATAG | 257397 |
rs781524326 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30846754 | TATTACCAAGAATAC[A/G]GCCTTAGTCCATAAG | 257397 |
rs781598195 | snp | C/T | 0.00791544 | 0.0624105 | intron-variant | TAB3 | GRCh38.p7 | X:30872909 | ACCCCTCCAAGAAAA[C/T]ATATTATGAACCTAA | 257397 |
rs781599152 | snp | C/G | 0.00158814 | 0.0281345 | intron-variant | TAB3 | GRCh38.p7 | X:30850760 | ACATCAATAAGAGCT[C/G]TGATATAAAATCTGG | 257397 |
rs781614071 | in-del | -/A | 5.29262e-05 | 0.00514396 | intron-variant | TAB3 | GRCh38.p7 | X:30855581 | GGGGAGAAAAATGGT[-/A]AAAGTAACATTGGCA | 257397 |
rs781644415 | snp | A/G | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30850146 | TGAGAGCCTACTCAC[A/G]GTCTCAACCACCACG | 257397 |
rs781655897 | snp | C/T | 0.00211696 | 0.0324653 | intron-variant | TAB3 | GRCh38.p7 | X:30873577 | GCCTCTCCTTCCACC[C/T]CCTCCCCTTTTTCTG | 257397 |
rs781663427 | snp | A/G | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30841956 | TGGGATTACAGGCGC[A/G]CGCCATCAGGCCTGG | 257397 |
rs781664260 | snp | A/G | 0.00370173 | 0.0428621 | intron-variant | TAB3 | GRCh38.p7 | X:30832994 | TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTT | 257397 |
rs781666427 | snp | A/G | 2.46545e-05 | 0.00351093 | synonymous-codon, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855527 | GCTACTCTCCTGGGA[A/G]AGGGCTCGGCAACAG | 257397 |
rs781667668 | snp | C/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30850044 | ATACCACACATTTTA[C/T]AGATAAGAAAACAAG | 257397 |
rs781701856 | in-del | -/TATAAA | 0.00528398 | 0.051128 | intron-variant | TAB3 | GRCh38.p7 | X:30841519 | TACTATGTTGCAACT[-/TATAAA]TAAAAAAAAAAACAC | 257397 |
rs781729140 | snp | G/T | 0.000529661 | 0.016265 | utr-variant-3-prime | TAB3 | GRCh38.p7 | X:30828959 | CCAGATTTATCAGTG[G/T]CAAGTCATTTTGCCT | 257397 |
rs781741699 | snp | A/C | 0.000529661 | 0.016265 | intron-variant | TAB3 | GRCh38.p7 | X:30865196 | ATGAAAGGTATTTAG[A/C]ATTCTGGCCCCGCCC | 257397 |
rs781770953 | snp | G/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30832528 | GTAACAAAAGAAACA[G/T]ATCTAGGGAAGCTTT | 257397 |
rs796188891 | snp | A/C | | | missense, nc-transcript-variant | TAB3 | GRCh38.p7 | X:30855479 | ATTCATCCTATTGTC[A/C]TCTGGACTATGGTAT | 257397 |
rs796289562 | in-del | G/TT | | | intron-variant | TAB3 | GRCh38.p7 | X:30864803 | TGTGTGTGTGTGTGT[G/TT]TTTTTTTTTTAAAGT | 257397 |
rs796377945 | in-del | GTG/T | | | intron-variant | TAB3 | GRCh38.p7 | X:30864805 | TGTGTGTGTGTGTGT[GTG/T]TTTTTTTTAAAGTTG | 257397 |
rs796530502 | in-del | -/T | | | upstream-variant-2KB | TAB3 | GRCh38.p7 | X:30890282 | TCCTTTTTTTTTTTT[-/T]GAGACCGAGTCTCAC | 257397 |
rs796729284 | in-del | -/AAA | | | intron-variant | TAB3 | GRCh38.p7 | X:30859697 | TTTAAAAAAAAAAAA[-/AAA]GTATGGTTAAGTCTA | 257397 |