SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs113320778 | snp | C/T | 0.444444 | 0.157135 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009509 | TATATGATCATGCTA[C/T]TTATGACAGATTTAC | 114088 |
rs113323285 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025030 | CCTCAGTGTGGAAGA[C/T]AGGAACCAGTTGGAA | 114088 |
rs113384212 | in-del | -/TC | 0.5 | 0 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095288 | GGGGGTTCGGTAGAG[-/TC]TGAGGATAGGGCAGT | 114088 |
rs113418439 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097031 | GCTGTTACACTTTGT[A/T]TGAGTTTGAACTCTG | 114088 |
rs113419082 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052026 | AGAGGAAGGGAGGGG[A/G]GGGGAGGGGAGGGAA | 114088 |
rs113421235 | snp | A/T | 0.0399052 | 0.1355 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077375 | TGGCCCTCAGTCTCA[A/T]CTCCAATTCTGTTTT | 114088 |
rs113474490 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038535 | CTCCTTTTAAGTTGG[A/C]GAGAGGAAAGCCTTA | 114088 |
rs113479358 | snp | A/G | 0.0607341 | 0.163335 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071093 | TCACCTAAGAAAGTG[A/G]AGGCGGCCAGGCACA | 114088 |
rs113561726 | in-del | -/A | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089883 | CTGTTTGACATGAAT[-/A]GTTTATGGTTGTGTT | 114088 |
rs113571366 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088597 | CTCCCTGTCTGGCCT[A/T]ATGTTCTTAAAAGTG | 114088 |
rs113585546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036134 | GCCCCGAGGCAAAAA[A/G]TGGCTCTTCCACCTC | 114088 |
rs113607832 | snp | G/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991204 | TTTCAATTACATACA[G/T]AGGATTCCAAAGAAT | 114088 |
rs113623348 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029453 | TTCCCAGGTACAAAG[A/G]TAAACACAACACTCA | 114088 |
rs113663586 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089105 | TCCAACCTGACTGAT[A/G]CTGAGAGTGAACTTA | 114088 |
rs113688819 | in-del | -/TTGTTGTTG | 0.52644 | 0.17219 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054297 | CCTATTTATACTCAT[-/TTGTTGTTG]TTTGTTGTTGTTGTT | 114088 |
rs113690989 | snp | A/C | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068006 | TTGCTGAATACATGA[A/C]TTAAAGTTTTCAAAC | 114088 |
rs113692650 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096290 | GAGAGAGGGAGGAAG[A/G]AAGGGGGGGGGAAAG | 114088 |
rs113704583 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015510 | CTTTACTTTTCTTTT[C/T]TTTTTTTTTTTTTTT | 114088 |
rs113712294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015781 | AAAGCATTGGGATTA[C/T]AGGCGTGAGCCACCA | 114088 |
rs113736848 | snp | C/T | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042619 | CTGATGTTACAAAGG[C/T]AAACCCGATATTATC | 114088 |
rs113767178 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096289 | GGAGAGAGGGAGGAA[A/G]GAAGGGGGGGGGAAA | 114088 |
rs113785288 | snp | A/G | 0.125182 | 0.216612 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039806 | GGCTGGAGTGCAGTG[A/G]CGCGATCTCAGCTCA | 114088 |
rs113787131 | in-del | -/A | 0.0132536 | 0.080319 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010502 | GAACCACCTAGGATT[-/A]AAAAAAAAAACAACA | 114088 |
rs113809928 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094036 | ACTGGGATGCGCTGT[G/T]CGCAAGAGACGGGGA | 114088 |
rs113821638 | snp | C/T | 0.153 | 0.230415 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992367 | AGGATCGCTTGAGGC[C/T]GGGAGTTTGAGACCG | 114088 |
rs113841501 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091507 | AAATTCTGGCCCATG[A/G]GCTTTTGTGGAGATA | 114088 |
rs113862776 | snp | A/G | 0.5 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001316 | CTCACTGCAAGCTCC[A/G]CCTCCCGGGTTCACA | 114088 |
rs113891951 | snp | C/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095301 | AGTCTGAGGATAGGG[C/T]AGTCTTCGCTCGCGG | 114088 |
rs113892108 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081985 | GCCCTGGGGGTCAGA[A/G]GTCAGTGGGTGGCAC | 114088 |
rs114011368 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031759 | GTTGCTAGCCCTGCC[A/G]CTGACCCAGGGAGAG | 114088 |
rs114053151 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042958 | TACATACATGTCTCT[A/T]TATATCTATTCCTGG | 114088 |
rs114136023 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086838 | CACGGAGTGGATGAG[C/T]TTCTTGAGACAGGCG | 114088 |
rs114145147 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069283 | TTAAGTGGTTCATCT[A/G]TGTTAATCTAGACCA | 114088 |
rs114217658 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093608 | TCAGTATTCCGCCTG[C/T]GGCGTCTCCCCGACC | 114088 |
rs114221396 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074990 | TCACAAAGGCACAAG[A/C]AACAGGCAGCGGACA | 114088 |
rs114278820 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021125 | CTATAACAATAAAAG[C/T]TTTGGGTTTCTGAAG | 114088 |
rs114282737 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026218 | CCACTGTGGTTCCTG[A/T]CTTTAGGATGGATGT | 114088 |
rs114296511 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025728 | TCTAATTCTTATCAA[C/T]GTTACTTAGCACAAA | 114088 |
rs114325591 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088670 | AAAAAAAATCTCTTC[A/G]GCCTCTTTGTGAAAA | 114088 |
rs114358723 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077098 | TTCTCCTAGTTTATT[G/T]TCCATTAACTTGAAT | 114088 |
rs114433559 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068757 | GTGATGAGGCCAGCC[C/T]ATGTTGCAGAACCAA | 114088 |
rs114444674 | snp | C/G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006504 | GCTTTTTCTTTCCAT[C/G/T]GCAAGCATCTGACAG | 114088 |
rs114550639 | snp | C/T | 0.0107246 | 0.0724382 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976419 | TTGCTTTTTCTCCTA[C/T]TGGAATATAAGCTCC | 114088 |
rs114554601 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036335 | GGTTTGTCAGCACAC[C/T]ACTGTATATACTTCA | 114088 |
rs114627763 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054122 | AAAAAAAATTTTAGA[A/G]ACAAGATCTCATCAG | 114088 |
rs114695305 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034601 | ACGCAGTTTCACCTC[A/G]GGAAACAGGAATAAT | 114088 |
rs114753171 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033469 | TGTCATACCATGTCT[C/T]GACTGAGGGTTTGGT | 114088 |
rs114755812 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002301 | TGATTTTTTTTTTTT[C/T]TTTTTGGTATTTTTA | 114088 |
rs114769768 | snp | A/G | 0.0513262 | 0.151752 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083587 | CAGCATTCTTCACAC[A/G]TCTGTGGAGTTAAGA | 114088 |
rs114823155 | snp | G/T | 0.0134861 | 0.0810011 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975349 | ATCTGTAATTGCAAT[G/T]CAGTGTAAACTACAT | 114088 |
rs114832478 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000914 | AGAATGACAAGCATC[C/T]CCCTGATAAACACGT | 114088 |
rs114858746 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023464 | AAAGTACTTGCCCCT[C/T]TCATTAAGGAAAGCA | 114088 |
rs114885199 | snp | G/T | 0.00398564 | 0.0444627 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975225 | AAAGGTGAATTGTCA[G/T]CCGCAATAGATAAAA | 114088 |
rs114922100 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077205 | AGCACTGATTTGTCT[A/G]CAGTGTAATGGCATA | 114088 |
rs114978809 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979213 | GGTGCTTATGCTTGG[C/T]GTGGAATAAAATAAG | 114088 |
rs115020092 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092094 | AAGGATACTTTGTAG[A/G]GCAATTCAACATGGA | 114088 |
rs115020569 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083760 | CTTTAGGGTTCAATG[A/C]AAAATGTTTGATTAG | 114088 |
rs115069869 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053952 | AATCACTAATAAAGC[A/G]TGTTATCAGTTTAAT | 114088 |
rs115071767 | snp | A/C | 0.0509478 | 0.151255 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081168 | TAAAAGACAGACAAC[A/C]CAATTAAATGAGAGC | 114088 |
rs115141764 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977727 | CAGATTCGCAGAGAC[A/G]GCACTTCCCTTATTA | 114088 |
rs115157674 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011232 | TCTCTCTGAGCAAGC[A/G]GTTTCTGCTTCTAAG | 114088 |
rs115193234 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042136 | ATAGCTAAATCAACT[C/T]CCTCACTCCAGCATG | 114088 |
rs115242569 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997327 | AGTATAGCTAAGAAG[C/T]AAAAATTCTCTAGAG | 114088 |
rs115270712 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050997 | ATGCTGCTGATTCCT[A/G]AGCACAGAAACTGTG | 114088 |
rs115278542 | snp | A/T | 0.0168055 | 0.0901129 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061645 | GAGCTTAATGATTGT[A/T]GCTTATACTTTTAGG | 114088 |
rs115300778 | snp | C/G | 0.0267878 | 0.112589 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095206 | GCGGCCCATTGGGCG[C/G]GGGGCAAGAGATCGA | 114088 |
rs115393019 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986594 | TTTTTTACAAACTGT[C/T]TCCTATTCCATATTT | 114088 |
rs115450763 | snp | C/T | 0.0829062 | 0.185956 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083032 | ATGGTTCTTGCCTCA[C/T]GGAGTTGTGGGAATT | 114088 |
rs115474889 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979088 | TGGTTAAAGGCTTTC[A/G]TTTCTATTTAGAGGT | 114088 |
rs115475057 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012718 | CATCCTCGCCCACAC[G/T]TATTATTTTCTGATT | 114088 |
rs115538421 | snp | G/T | 0.00153587 | 0.0276691 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979284 | TCTTGGTCTGGGCCT[G/T]ACGCTGTCAGCTTCC | 114088 |
rs115556053 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054605 | TTTTTTTTTTAGAAG[A/G]AGTTTCGCTCTGTCG | 114088 |
rs115580250 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090509 | GACAAGATTAAGAAT[A/G]AATAGTGTTTAGAAT | 114088 |
rs115585297 | snp | A/T | 0.0252325 | 0.109451 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031213 | TTCTATCCTTGACCA[A/T]GTTATAGCCAGGGTC | 114088 |
rs115641350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031688 | TAAAATCTGTCCTTT[C/T]TACACATTAAAATCT | 114088 |
rs115695881 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998604 | TCCATCAGTATGGTT[C/T]GTAAAAAACATGTTT | 114088 |
rs115708511 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985809 | AAGCTCCACCATCCC[A/G]ATGCTCCTCATACGG | 114088 |
rs115762966 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977491 | CTAGCAGGCATTAAA[C/T]GGAATTCAAGAAGAA | 114088 |
rs115769666 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014266 | GCTATCTGAGTGCTG[A/G]GGCTCTCTGCTGACT | 114088 |
rs115777729 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058344 | AAAAGGTATTTCTGC[C/T]TTGCCTACTCTAACG | 114088 |
rs115778158 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039212 | CATGGAACATCTAGA[A/C]CCTCACATGTTGCTA | 114088 |
rs115836152 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054319 | TTGTTGTTGTCCAGG[A/C]TGAAGTATAGTGGCT | 114088 |
rs115899369 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051462 | GAAGAGGAATTTGGG[A/C]CAGGTCGGGTGAGGG | 114088 |
rs115899760 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041011 | ATTCAGTACTTATAG[A/G]TCAATTTCCTTCCAC | 114088 |
rs115965638 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052102 | AAGAAAGGAATAGTC[A/G]AACCATCCAGACTTA | 114088 |
rs116008477 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080174 | ACATGTGGAAACTCC[C/T]ACCAATAGATTGATC | 114088 |
rs116012226 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001123 | TCATCCCCTTGAACA[C/T]TGAAGACATTATCCC | 114088 |
rs116017431 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030274 | AGCTGAGCTGTCCAA[A/G]GGTCCTGATTCCCCC | 114088 |
rs116069951 | snp | A/G | 0.330482 | 0.236691 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992418 | CCCTGTCTCTACGGA[A/G]AAAAAAAAAAGCCAG | 114088 |
rs116081295 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052476 | TATTTATTTTTGGCT[A/G]TTGTTGCTATTAGCG | 114088 |
rs116140443 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061457 | GACTTTTTATTGTAA[A/G]GATATACATATTGAA | 114088 |
rs116190933 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977515 | AGAAGAATCCTGCCT[A/G]TGGTAACAGGCTGCT | 114088 |
rs116232582 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058606 | GCCACTGGGGTGGTG[C/T]GCTGGTGAGCCACCC | 114088 |
rs116260351 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025698 | AAAAGCAAAACAAAA[C/T]AGTGAGTCAGATGAT | 114088 |
rs116375069 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038435 | AAGGCAGTTGGTTAA[A/G]AGCTGGATGCTTACC | 114088 |
rs116384955 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074105 | TAATGATCATAACAA[C/T]GAAACCAAACATCTG | 114088 |
rs116416325 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063765 | AAATTAACGGAAAAG[A/G]AAGACATTTTTAGAT | 114088 |
rs116447888 | snp | C/T | 0.0244538 | 0.107838 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054134 | AGAGACAAGATCTCA[C/T]CAGGCTGGCCTGGAG | 114088 |
rs116461719 | snp | A/G | 0.278664 | 0.248351 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096302 | AAGGAAGGGGGGGGG[A/G]AAGGAAAGGCGGAAG | 114088 |
rs116543007 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085598 | GTACAAGAAAAAACT[A/G]AAAGTAAACAGATAC | 114088 |
rs116564903 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018963 | ATTTCAGGGTTATGT[C/T]AAATTGTGAATGTTA | 114088 |
rs116566903 | snp | A/G | 0.0232847 | 0.105357 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051438 | AACTAGCACTGTGGA[A/G]AAAGGGTGGAAGAGG | 114088 |
rs116602579 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090996 | TAGTAGTGGTTTCTA[G/T]TGCCCATTTTAAAGT | 114088 |
rs116659476 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026162 | TGAGAAAGCTTTTGC[A/T]TTTCTGCTGATACGG | 114088 |
rs116660550 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052454 | CAACAACCCCAGCCC[C/T]TGGAGTTATTTATTT | 114088 |
rs116689251 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987035 | GCTGGTTCTATGCAC[A/G]GTGTGGTCTAGTCAG | 114088 |
rs116718770 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007617 | CCCAGTTTCTTCAAC[C/T]GTCTACTAGGGTTAT | 114088 |
rs116722940 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004861 | GAGGAAAGTCTGCAC[A/G]TCTAATTCCCAAAGT | 114088 |
rs116750664 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024223 | TGCTCTGATGAAGAG[A/G]CCCGGGCAGAGGCAA | 114088 |
rs116757572 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028603 | TTTTCATCACGGCAT[C/T]TTTGGTGGTACAAGC | 114088 |
rs116819918 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066020 | TACTGATTATTTTCA[C/T]TGGCGTGCAAGCAGG | 114088 |
rs116875219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020466 | GTTTCTGCAGTCCTT[C/T]GAGGTCTGGGCAGGA | 114088 |
rs116966185 | snp | A/C/G/T | 0.0206011 | 0.0997516 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982592 | TTTGAAGTCTTCCTC[A/C/G/T]GCTCTAGTGAAAGCT | 114088 |
rs116968429 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005009 | GTAGACTGTCATTCC[C/T]CTTTATGGTGGCTGA | 114088 |
rs117003314 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019220 | GGTCCAGTGTGCTCT[A/G]CTCACTGTTGGAATA | 114088 |
rs117037333 | snp | A/T | 0.0244538 | 0.107838 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038130 | AGATTATCCTGGATT[A/T]TCTAGGTGGGCCCAA | 114088 |
rs117053911 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058208 | TGTCCCTGCATTACA[G/T]GATGGCACAATCATG | 114088 |
rs117057713 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017587 | AGTCCCAACCACACA[A/G]GAGAACATTTACCAC | 114088 |
rs117061936 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982210 | AGCGTTTTCATGCTG[C/T]CATGCAGGAAGGAGG | 114088 |
rs117134921 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998592 | CTGAGCTCCTTATCC[A/G]TCAGTATGGTTTGTA | 114088 |
rs117212610 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007632 | TGTCTACTAGGGTTA[C/T]GAGAATAAAATGAGT | 114088 |
rs117281002 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042806 | AGACTAACCTACTCT[A/G]GTACAGACCTGCTCC | 114088 |
rs117297985 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029512 | ACTTTGAGGGAAGGC[C/T]GCCAAGGAGAATAAC | 114088 |
rs117357006 | snp | A/G | 0.0165278 | 0.0893908 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055811 | TTATGACAGGGATAA[A/G]GAAACTAATACAATG | 114088 |
rs117359002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054629 | TCTGTCGCCAAGTTG[A/G]AGTGCAGTGGCGCGA | 114088 |
rs117387411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049994 | TGACAAGCTAAATCA[C/T]ATAGGGATTTGTAGG | 114088 |
rs117464517 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064801 | TGAACCAAATGGAGA[C/T]AAGAAGCAATATAAC | 114088 |
rs117480727 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008810 | TGATGATCTCTTTCT[C/G]TCTCTGCTTTCCTCT | 114088 |
rs117572731 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040808 | ATTACATTTACAAAG[C/G]CTGAATTTAAATGAC | 114088 |
rs117635477 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086822 | AAGCAGGAATTGAAA[C/T]CACGGAGTGGATGAG | 114088 |
rs117757398 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042899 | CCTCCTTTAACCTTC[A/G]TTCTACTCTGTTCTA | 114088 |
rs117792449 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089877 | ATTGACTCTGTTTGA[C/T]ATGAATGTTTATGGT | 114088 |
rs117798494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987957 | AGGCGTGAGCCATCA[C/T]GCCCAGCTAATTTTT | 114088 |
rs117818891 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987707 | CAAAATACAACACCC[A/C]AGCACCACAAACTGG | 114088 |
rs117848199 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091317 | TAAGATGATGATTTA[C/T]GCCTGTGGGAAATAC | 114088 |
rs117911556 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012832 | GAGCATCTTTTCATA[C/T]GTTTATCGGCTGTTT | 114088 |
rs118025360 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992205 | GACAGGTTCTTTGTT[C/T]CTCACAAGGTGACAG | 114088 |
rs118053017 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033547 | ACAATTTGCTCTGGT[C/G]CCATTTTGTCACATG | 114088 |
rs118131267 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010819 | TCTGTGAAGCTGACT[C/T]TGCTGAGCGATGTTT | 114088 |
rs137868073 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993789 | GGCAAATAGCACTTT[A/T]CTAATGTTAGCACCA | 114088 |
rs137911230 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996875 | GACTGACAACTGCTC[C/T]CCAAAGCACTGTTTT | 114088 |
rs137967157 | snp | C/T | 3.29696e-05 | 0.00406001 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094214 | GGGCATCTTGCATTG[C/T]ACGCAGTACATGCTG | 114088 |
rs137971468 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004860 | GGAGGAAAGTCTGCA[C/T]GTCTAATTCCCAAAG | 114088 |
rs137978521 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074247 | AACATAGCAAGACTC[C/T]GTCTCTACAAAAAAA | 114088 |
rs137995954 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041839 | TAATAAACATGTTTT[C/T]CCAATAACATTTATA | 114088 |
rs137996573 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032365 | TTCTCTCAAAGACTA[C/T]GCATCCTTCTCCCAG | 114088 |
rs138045229 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977419 | CTTTACACAGTGTAC[C/T]GTGGGTGTGTCCCTA | 114088 |
rs138085159 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078658 | AACATACAACGATAT[C/T]GTATGATATTTTAAA | 114088 |
rs138102464 | in-del | -/A | 0.0486741 | 0.148216 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064165 | AGACTGTGATCAATT[-/A]AGAACATAGACTGTG | 114088 |
rs138115714 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026966 | TGCCAGTTACTGGCT[-/G]GTTCAACCCTTTATA | 114088 |
rs138127776 | snp | A/C | 0.0232847 | 0.105357 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051590 | GTGGGTGTAATTAGC[A/C]GAGGAGTATAATGCA | 114088 |
rs138134702 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985729 | ACTCATCACTTTCTA[A/G]TGCCGTAATACATGG | 114088 |
rs138159052 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038286 | ATTCTCCTTTAGAGC[A/T]TCCGGAAAGGAACTC | 114088 |
rs138186173 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001071 | CCTTCATTGTGGCTG[-/TT]GGAGGGGAGACAGGC | 114088 |
rs138244239 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083721 | GGGAGTTGAGATACA[C/T]ATCCAAGTGGAGATG | 114088 |
rs138253295 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990676 | TGTGTCCTGGTAGAA[C/G]TCTGGGTTGTCCTCC | 114088 |
rs138268072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011047 | TGGGGGACCTGGAAG[C/G]CCAAGGTGGAGCTTG | 114088 |
rs138307198 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015043 | TAAAATTTTATCAGC[A/G]GAGCCACCATCTGTT | 114088 |
rs138367073 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022081 | TACTTTTAGAATTTT[G/T]CTTAGCACTTTTTAC | 114088 |
rs138395225 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056003 | AAGACAACCTTCATC[A/G]GAATGTATAAATTCA | 114088 |
rs138418775 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018739 | CCTCAGCATCCTCGC[C/T]GAGTAATTTTGTTGG | 114088 |
rs138465909 | snp | A/G/T | 0.000115305 | 0.00759217 | missense, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981868 | CATTGCCCAAGCTTT[A/G/T]TCGTCTTTTCCTAAC | 114088 |
rs138497251 | snp | G/T | 0.0225045 | 0.103662 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052631 | TTAAAGTAGGAATTC[G/T]GATGCAGGCAGAGGC | 114088 |
rs138533464 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069060 | TAGGTGAAAGGACAT[A/T]GGGGACTATGGTAAG | 114088 |
rs138545015 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069592 | ATGGTGAAGGCATGT[A/G]TTTGATTTGTTTCAT | 114088 |
rs138556152 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997766 | GGGGCACATTCAGGC[C/T]TTCATTTTTCAGCTT | 114088 |
rs138609643 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041468 | TGGCCCTCTTAGGAA[C/T]GTCAATGATGTTTCA | 114088 |
rs138620482 | in-del | -/CTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027132 | AATGCTGGCTGTTAA[-/CTTTTTTTT]TTTTTTTTTTTTTTT | 114088 |
rs138620950 | snp | G/T | 0.00676609 | 0.0577691 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974768 | GCACTTTGGGAGGCC[G/T]AGACGGGTGGATCAC | 114088 |
rs138640881 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042626 | TACAAAGGTAAACCC[A/G]ATATTATCTTTTTAG | 114088 |
rs138647830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032834 | TTAAAATTCAATAAG[C/T]AGTACAGGTTGAATA | 114088 |
rs138648886 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078312 | TGAACAAATACTAAA[A/T]GAAATTAATTTTCAA | 114088 |
rs138665052 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002144 | TTCTTTTTTTTGAGA[C/T]GCAGTCTCGCTCTGT | 114088 |
rs138672577 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991192 | AAAATTCCTGTATTT[A/C]AATTACATACAGAGG | 114088 |
rs138672738 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031724 | TACCACTTTAATTAG[A/T]GTCCAGCTAGTTAGT | 114088 |
rs138680353 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037491 | AAAAGCTAACTCACA[A/G]TGGTGATCAGATCAG | 114088 |
rs138695634 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090828 | GTCTTAAATCCTGGC[C/T]GCAAGAGATCTGACC | 114088 |
rs138724439 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982269 | GTCCTGGGAGTTGGT[A/G]CTCTCTGCACCAGAA | 114088 |
rs138725345 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005427 | TGTTTCGTCCTGGTT[A/C]AGAATGAACAAACTG | 114088 |
rs138777984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074578 | TCTCATTTTAGGAAG[C/T]AAATAGTCCAAAATG | 114088 |
rs138845267 | in-del | -/GAAAA | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035043 | TATAACACATTAAGT[-/GAAAA]GAACAGATTTCAAGA | 114088 |
rs138856093 | in-del | -/AATG | 0.464416 | 0.128553 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992582 | GTCTCTGGAAAGATA[-/AATG]AATGAATGAATGAAT | 114088 |
rs138862415 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049554 | TAATATAGGCCGGGC[A/G]CAGTGGCTCATGCCT | 114088 |
rs138862773 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051943 | CTGCACTCCAGCCTA[A/G]GCAACAGAGACCCTG | 114088 |
rs138873084 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052043 | GGGAGGGGAGGGAAA[A/G]GAAGAGAAGAGAAGA | 114088 |
rs138913890 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990473 | CAGTGTCATATATTA[C/T]TGATTGGTTTTTACA | 114088 |
rs138922909 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087510 | GCCCAGTTTAGGGTT[C/G]TGAGAACACCCCAGG | 114088 |
rs138960206 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062348 | GTCATATTTTTCTCG[A/T]TTTTTTTGTATGTCT | 114088 |
rs138964743 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987013 | CTTTCTATTTTGTCA[A/G]ACAATAGCTGGTTCT | 114088 |
rs138980578 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978296 | TCTCAAGACAACCAT[C/T]TGTGGAATGAGGCTC | 114088 |
rs138991454 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092603 | AAAAGCTCCTTCCAA[A/C]CATCCTGAATCCCTG | 114088 |
rs138998894 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978522 | TCTGGAAGGCTCCAC[A/G]CAACTCACTCCCTCA | 114088 |
rs139002960 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045358 | CATAAAACAATCTTT[C/G]TTATGACAAGACAGA | 114088 |
rs139005603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019696 | CAATAACAGTTAATA[C/T]ACATTAAAGATTGTG | 114088 |
rs139023897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092353 | GGATCACATTCAACC[A/G]GGTTAAGGAGTTGAG | 114088 |
rs139045265 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048329 | TCTCAGCTTACAGAC[A/C]CTGTGGATAGGAGCC | 114088 |
rs139052661 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046599 | CTTCTATTCTATAAT[A/G]GAGAATTTTAAAAAT | 114088 |
rs139064993 | in-del | -/ACACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080437 | ATTGAGTTTTATTGA[-/ACACAC]ACACACACACACACA | 114088 |
rs139100561 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993371 | TTTTCAACAAGACTC[-/T]CTTTTTTTTTTTTTT | 114088 |
rs139123393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024732 | CTAAGCAGAGGAGAA[A/G]CATTATTGTGGGTCA | 114088 |
rs139141671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084435 | GGTAGCCGGATGACA[C/T]AAGGTAGTGTGTAAA | 114088 |
rs139277076 | snp | C/T | 1.65359e-05 | 0.00287536 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998200 | CCTCCTGAGAGTCAG[C/T]AAAGAACAGGACAGC | 114088 |
rs139301019 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045618 | AGAGTAAATGTGAGA[A/T]TACTGTCATTATTGT | 114088 |
rs139303572 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998129 | GACCCGAGCGTTGTA[C/T]GTGCTGTTGAAGTGA | 114088 |
rs139362826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979668 | TCACTACCCCAAAAC[C/T]GTTTCCCTAATCATC | 114088 |
rs139400051 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081586 | CAGAGTTAGACTCCA[C/T]AGCAGTAAAGGATCA | 114088 |
rs139401309 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993517 | GGGATTACAGGCGCC[C/T]GCCACCACACCCAGC | 114088 |
rs139447018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994634 | GTTCTCAGCCCTGTA[C/T]GATTTTTTAAAACAG | 114088 |
rs139449497 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988302 | TACTGAACACAGACC[G/T]TGGGGAGTGTATCCA | 114088 |
rs139468382 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995639 | TTACCGCATATGAAA[C/T]TTTACCTTTCTGTGA | 114088 |
rs139474541 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066831 | AACAGGTGGTCGCCT[C/G]CGATTGACTGAAGCT | 114088 |
rs139476999 | snp | G/T | 8.37051e-05 | 0.00646881 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998066 | CTCAGACGTTTGGAG[G/T]ACCAGGGTCTTGCTG | 114088 |
rs139555188 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053980 | AATCAGCTACCATCT[C/G]TAAAGATAGATGAGT | 114088 |
rs139585956 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991526 | TCTGGGTCAGGAAAA[C/G]CAGAGACAGAAAAAC | 114088 |
rs139595919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058288 | CTGAACATCCTTGAG[C/T]TAGTTACTCAGGTGA | 114088 |
rs139662878 | snp | G/T | 0.0244538 | 0.107838 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016424 | GAATCTAATGCCTGA[G/T]GATCTGAGGTGGAAC | 114088 |
rs139689490 | in-del | -/TTAGTAT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031910 | TACTAAACAAATCTC[-/TTAGTAT]ACCATTTGTATTGTG | 114088 |
rs139757771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049651 | GCCAAAATGGTGAAA[C/T]GCCATCTCTACTAAA | 114088 |
rs139758405 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007355 | TATTTTACAGGCTAC[C/T]ACACTGGTATTAAAA | 114088 |
rs139766969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011563 | TATTCATACTACTTT[A/G]CAAAAGCCTAAAATA | 114088 |
rs139778943 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012494 | GAATACTTTTGGCTA[C/T]TGTGAATAAAGTGAT | 114088 |
rs139787567 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013654 | ATTTTTGTGAGTTTT[A/G]GGGGGATCAAATTTA | 114088 |
rs139791188 | snp | A/G/T | 0.000386735 | 0.0139007 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094403 | CTGTTCGCACATGAC[A/G/T]GTGGCTTCCTTGGGC | 114088 |
rs139811584 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999997 | GGGGATAGGGCTCCC[C/T]CACCTTGGGAAGGTA | 114088 |
rs139833871 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085699 | AAGATACTTAAAATG[C/T]CTATGGATTTTTATT | 114088 |
rs139952049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075799 | TCTCATTGCTCTTGG[C/T]CACCTTCTGACTAAC | 114088 |
rs139964076 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043749 | AATGAAACTGAGAAG[A/G]GCTGGTAGCCGAGAT | 114088 |
rs139968469 | snp | G/T | 0.030278 | 0.119257 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002351 | GTGTTAGCCAAGATG[G/T]TCTCGATCTACTGAC | 114088 |
rs139971297 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070684 | AAGAATACTCAACCT[G/T]CACTGGGAATAACAG | 114088 |
rs139994655 | snp | C/T | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079273 | TCAGAAGAGAATAAT[C/T]GGCCAATCTTTGGCT | 114088 |
rs139999790 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029350 | TGCCTCCCCGGGCGT[C/G]GGGCACCTTCTGGTG | 114088 |
rs140041343 | in-del | -/AAC | 0.250732 | 0.249999 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068349 | AAAAACAAAAACAAA[-/AAC]AAACAAAAAACAAAC | 114088 |
rs140111719 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983144 | TTTAGTGCTCATAAA[A/C/G]AGTGCTTTGCACTGA | 114088 |
rs140175142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016948 | TGTTTGTTCTCCATG[C/T]GTCCTTTTGATCAGG | 114088 |
rs140178821 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086660 | AATTATAATACAGTG[C/G]GAGGATGCTCAGGGT | 114088 |
rs140193012 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014152 | CAGTTCAATGATGCA[C/T]TCATGTACTGAAATA | 114088 |
rs140203214 | snp | A/T | 0.0178098 | 0.0926698 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073753 | TCAGTTTGTGGAAAT[A/T]CATTGAAATGTACAT | 114088 |
rs140213263 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004463 | CAGTGATCTTTCAGA[C/T]TGTGAACACTCACAA | 114088 |
rs140218289 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001276 | GCTCTGTCGCCCAGG[C/T]TGGAGTGCAGCGGCA | 114088 |
rs140226954 | snp | A/G | 1.76605e-05 | 0.00297152 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977347 | GGAGCCCGGTGTGCA[A/G]CGTGACCTGGGGAAT | 114088 |
rs140274200 | in-del | -/CAAA | 0.0178098 | 0.0926698 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005556 | AAATCTATTCTCAAC[-/CAAA]CAGTAAAGCCCTTGG | 114088 |
rs140280296 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041555 | CCCCCAACTGCCTTT[C/T]GCCTGATTTCCAGCA | 114088 |
rs140301644 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044033 | AATTGAATCAGGTTA[C/T]GTGTTCTGTCCATGA | 114088 |
rs140323025 | in-del | -/CAGATCTGTTTCAGACAAT | 0.133093 | 0.220981 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086781 | GGGGACTGAAATGAC[-/CAGATCTGTTTCAGACAAT]CAGGTACAAGCAGGA | 114088 |
rs140350667 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047369 | CATTTCATCATGGCT[-/G]GTTTCCCACTGGAGC | 114088 |
rs140366325 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083151 | TGATAGACTAGAACT[A/C/T]GATACTTTTCTCATG | 114088 |
rs140381945 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018068 | GACTTCTGCTGAGGG[C/T]AGTTGAAAGCTTCAA | 114088 |
rs140399927 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020297 | GAGCCGTGGAGGCCT[G/T]TATCAGTGGTCATGA | 114088 |
rs140423041 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021848 | CAGTCCTGCCAATAG[G/T]GTCCCATTCTAATAG | 114088 |
rs140463293 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059083 | CAGGCCTATGACCAA[C/G]CCCAATATCAGCACG | 114088 |
rs140507223 | in-del | -/T | 0.400325 | 0.199756 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029777 | CCGAGAGGATACCCC[-/T]GAGTGAAGGTTTCAC | 114088 |
rs140572763 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026547 | GCACTGTCTTCTTTT[C/G]AAATTAAAGCCTATT | 114088 |
rs140593202 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990479 | CATATATTATTGATT[G/T]GTTTTTACACTTCTG | 114088 |
rs140595354 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055552 | AGGGGATGTGACTAC[A/G]GATGAATGGTTAGAG | 114088 |
rs140605080 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068541 | AATTCTCACCACAAC[C/T]TTGTAGAAGTTATTT | 114088 |
rs140616044 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040296 | ATATTTGATGCTGGT[G/T]CCCCTCACTCAGAGG | 114088 |
rs140624265 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061239 | CCAACCTAGTGAAAC[C/T]CTGTCTCTACGAAAA | 114088 |
rs140767326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047383 | CTGTTTCCCACTGGA[A/G]CTCCTTGAGGATAAG | 114088 |
rs140776674 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981604 | GAGTAGGAAAGTACT[C/T]AAGTCTCTATCATTA | 114088 |
rs140787804 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037163 | TTACTTACTAGTTAC[C/T]ATCTCTTGGAAATTA | 114088 |
rs140809802 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039570 | TAAATGAAGTTCAAG[A/G]ACAGTTTGATGGCGA | 114088 |
rs140849163 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976128 | TCTTTTTTTTTTCAA[A/C]TGTCAATTTTTAAGG | 114088 |
rs140850528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089608 | TGAAAAAAACGGAGC[C/T]TTATCAGCTATTTCA | 114088 |
rs140850984 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042895 | CCTGCCTCCTTTAAC[C/T]TTCGTTCTACTCTGT | 114088 |
rs140880248 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985630 | CCGCCACTCAGCCAG[C/T]GCCCGTGCCGTGCTA | 114088 |
rs140881734 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081191 | ATGAGAGCAAAGACT[G/T]TAAATAGACATTTCT | 114088 |
rs140882967 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004975 | ATTTTACTGTGTTAT[A/C]TTCTCTGAAGGCTCA | 114088 |
rs140889006 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077703 | CCGGCTGTCCTAAAC[C/T]AATTCTAATGAGTCT | 114088 |
rs140919444 | snp | A/T | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008189 | GGTGGCAGGAGGGAG[A/T]TCTTCATTCTGTATC | 114088 |
rs140927810 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082041 | CATTTGGTCTTTCCA[A/G]TGACCAAAAGATTCT | 114088 |
rs141023749 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993178 | CTGCCAGCCAAGAGT[A/G]TCCACTGGTACCAGT | 114088 |
rs141042537 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076476 | ATAAGCATTTCAGCC[A/G]TTCTTTCCATGCTTT | 114088 |
rs141107063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003718 | AGACAAATTAGCAAA[C/T]GGACAAAAAGTCAAA | 114088 |
rs141166484 | in-del | -/G | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095559 | CCGCGGGCGAGTGCT[-/G]GCGCAGCACGGAGGA | 114088 |
rs141169306 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990111 | CAGCCTTGAACTCCT[A/G]GGCTCAAGGGATCCT | 114088 |
rs141176004 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057698 | TTTTCTTCTCTATTT[G/T]TGTGGTAAAAATCAA | 114088 |
rs141286145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022364 | CCTTCTGCCTTCTGC[C/T]ATGGGATGATGCAGC | 114088 |
rs141287444 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984830 | TTACAAAGACTGTAA[C/T]GATATTTCAGTACAT | 114088 |
rs141289685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051028 | AGAGATAATGAGTTG[C/T]TTTTAGTTATTAAGT | 114088 |
rs141305560 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026108 | CACAATCCTGACGGA[C/T]GACACCTAAGTGGAA | 114088 |
rs141306424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985987 | CTGTAAAGAGGAATG[C/T]AAGCTCAGCTGGTGG | 114088 |
rs141329193 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045006 | GGATAATTTATTTGT[C/T]TAAGAGGGCGGTTGG | 114088 |
rs141369321 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005339 | AATACACCCTTAGGT[A/G]AGTAGAGGCACTTAA | 114088 |
rs141450731 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088450 | AAACTCGTGGGAGCA[A/G]AGTTTGAGAAATGCT | 114088 |
rs141460142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047686 | AGGAAAGAAACGCAT[A/G]TAACAATCTGTATCA | 114088 |
rs141460959 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016339 | CAGCAGCGGCATTAG[A/T]TTCTCACAGGAGCAG | 114088 |
rs141480436 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978691 | TTAACATTGTAATTA[G/T]GCTTATTATTTATTG | 114088 |
rs141566652 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019406 | TAACTATAATTTACA[C/T]TTCAAACAGTTTCCC | 114088 |
rs141577322 | snp | C/G | 0.00101029 | 0.0224527 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094907 | GAAGGAGCCGCACAC[C/G]GGGCATTTCAACTCC | 114088 |
rs141586530 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048508 | CTAGTGAAAGTCATT[G/T]GTTAATTACTAGTGA | 114088 |
rs141607470 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997313 | ACCAAAATATTTAAA[A/G]TATAGCTAAGAAGCA | 114088 |
rs141610603 | snp | A/G | 0.00088309 | 0.0209944 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982087 | CGCCGAGCCAGGGTC[A/G]AAAGCAAACCAGGCC | 114088 |
rs141615701 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995120 | ACCTCCCAAGTATCT[-/G]GGATTACAGGCATGA | 114088 |
rs141698653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000557 | TTCAGGTGAAGGGCA[A/G]GCAGGCCCTGCCAGG | 114088 |
rs141757878 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028330 | AAATTGAGGAGACAA[C/T]GAAAAATCCTGGAAA | 114088 |
rs141767867 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083388 | GGATCCTCAGTAGCT[C/T]GGACTACAGGCATGC | 114088 |
rs141789479 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041938 | TTCCATGTAACCTTG[A/T]ATCGCCGAATCCATT | 114088 |
rs141796240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037861 | GGGAGGGTAAAAGCC[A/G]TTCTTGTTACATGTA | 114088 |
rs141815045 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074917 | ATCTCCTTTTGATCT[C/T]ACAATGTTGAAGCCC | 114088 |
rs141831286 | snp | C/T | 1.66018e-05 | 0.00288108 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998084 | CAGGGTCTTGCTGTA[C/T]GGGCTGACTCCTGTT | 114088 |
rs141860472 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078344 | TCCAATATTTATACA[A/C]ATTTTATAGTAACCT | 114088 |
rs141871743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996632 | CCATCACCAGCAAGG[G/T]CCTTCTGCGTTGCAT | 114088 |
rs141874435 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049475 | TTCAGAAAGAGTTAC[C/T]ATCCATTTGTTTGTT | 114088 |
rs141874572 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027851 | TCTTTTTTTTTTCCT[G/T]AATGAGTAAAAGTTT | 114088 |
rs142001037 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987529 | ATGGAGTCAAGACTT[C/T]GTGTTCCCACTAAGA | 114088 |
rs142007341 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069124 | GAGAACTGATGGACT[C/G]TAGAAATGGAATCAG | 114088 |
rs142098790 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050426 | GTAAGACATGCCTTT[C/T]GCCTTCCACCATGAT | 114088 |
rs142129131 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017785 | TGAGACTGACTTTGA[C/T]TGGCATTGCCAAAGT | 114088 |
rs142156620 | snp | C/T | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010410 | CACTAGGATCATTTT[C/T]CTTAATCACCTCCAA | 114088 |
rs142195733 | snp | C/G/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051997 | GAGAAGGGAAGGGAA[C/G/T]GGAAAGGAAAGGGAG | 114088 |
rs142199379 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989946 | CAAAGATTGGCTGGG[A/G]ACCACTTGTATTATT | 114088 |
rs142216884 | snp | A/C | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092484 | GCTACCCTTTCTAGT[A/C]TCCAAGGAATTCTGG | 114088 |
rs142249958 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051256 | GTCTTTGCAAGAAAG[A/G]AAGAGAACAGTGAGA | 114088 |
rs142258610 | snp | A/C/T | 0.000296606 | 0.0121745 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009174 | CATCCTTGGAGTGAG[A/C/T]GTGCCTTTACCCCAC | 114088 |
rs142271229 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016373 | CCCTACTGTGAACTG[C/T]GCATGCAAGGGATCT | 114088 |
rs142288146 | snp | A/G | 0.0667028 | 0.170006 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033359 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 114088 |
rs142288765 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014978 | AAGCCTAAACCAGCT[A/C]CCACAGGACAGTGAA | 114088 |
rs142381360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087738 | TCATAAGTTGTTATG[C/T]TATGTTGTCCCCAGA | 114088 |
rs142400567 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081520 | CAGTGACTCCAATTT[A/G]CCGACATCCCTAGGC | 114088 |
rs142422752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067654 | GTGCTATTTCATCTG[C/T]TCGGCTGGCCCTTCC | 114088 |
rs142462794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006873 | CCTCTTACTTTTGTG[C/T]GCAGTCCTAAGTGGC | 114088 |
rs142495306 | snp | A/T | 1.65583e-05 | 0.00287731 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094134 | TTATGTAGTTTCCAC[A/T]TGGCCCCCAGAGCCT | 114088 |
rs142498585 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034995 | AGCTATTGAAAGGGG[A/G]TAGTAACATATTTAG | 114088 |
rs142537683 | snp | G/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089319 | TTCTATCCTTCTGTA[G/T]GCCAAAGTTAAGTTG | 114088 |
rs142544745 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017651 | GATGTTTTGTAGCAT[C/G]TGAAGTGTAGCAAGG | 114088 |
rs142553315 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991765 | TAAAGACTCAGAGGT[C/T]CTCAGCTGTAAGTCC | 114088 |
rs142563653 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981491 | CTTTTCTGTTAAGTT[G/T]TAGGTCTGGGTGTTT | 114088 |
rs142607099 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002010 | ACTTAAACTGCAAAT[G/T]AGTTGAGCCTTCAGA | 114088 |
rs142618659 | in-del | -/AT/GA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025758 | GGGCTATTGGTCTGG[-/AT/GA]GTAGGGCAGAAAGAA | 114088 |
rs142620382 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072741 | GAAAATCTATTTGCA[G/T]TCGTACTGTTTGCAC | 114088 |
rs142656008 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030806 | AGAGGAATCTTATGG[A/G]TAGGGATTTGCTCCA | 114088 |
rs142664807 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021183 | CAGTTTTTTAGCAAT[G/T]TTAGGCCAGGTGCTG | 114088 |
rs142667819 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998257 | GAGGGAGGCAGTGTC[A/G]CTCAGTGGTTAGGAG | 114088 |
rs142675656 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070250 | GCATGAGTTATAGTG[C/T]GATGGCTGTGAGTTC | 114088 |
rs142718893 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032158 | CAAAAAAATGTATCA[G/T]ACATGCCATTATTCC | 114088 |
rs142721000 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991329 | CCCTGGGATATCATG[C/T]ATGTGTCAAAATTTA | 114088 |
rs142734204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024446 | TAAAAATCCATTTCT[A/G]CCTTGACATGGTTAA | 114088 |
rs142755029 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027553 | TTGGAGAACATTTTC[A/G]ATCACCTGTACTTTG | 114088 |
rs142834038 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982860 | ACTCGAGAGATGTAA[C/T]TGCTGATTTATTAAA | 114088 |
rs142871831 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978318 | ATGAGGCTCATAGTT[G/T]TTAATGAGATGCCCA | 114088 |
rs142877288 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039310 | CAACTCTATGTGATA[A/G]CATATGTCCACGAAA | 114088 |
rs142960676 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085325 | TTCCCGCACCAAAGA[A/G]TAATGTTTAGCATTC | 114088 |
rs142977712 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976827 | CAGGTAAGCTGTATG[A/C]TACAAATTCAGCTCA | 114088 |
rs142979845 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043704 | GCAGCTCACTAATTA[C/T]ATGAATTCTTTTTAG | 114088 |
rs142997233 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018777 | AATTTACCAACCACA[C/T]ATGGAAACTGAAAGC | 114088 |
rs143017112 | snp | C/G | 0.0146672 | 0.084371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029873 | AGCCTCCCAAAAAAA[C/G]AGAATTCTCTCACCC | 114088 |
rs143019462 | in-del | -/ACACACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080437 | ATTGAGTTTTATTGA[-/ACACACAC]ACACACACACACACA | 114088 |
rs143022117 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041330 | TTGCACATGCAAGGG[C/T]GGGTTACACGAGGTG | 114088 |
rs143023201 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052754 | ACTCCAGACACAGAC[A/G]TCATTGCCCATAAAT | 114088 |
rs143042087 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001145 | CATTATCCCTAAAGG[A/C]AATGTTTTACATGGA | 114088 |
rs143043786 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005892 | TGTGGAATCAGAATG[C/G]GTCAGTTAAATCCGT | 114088 |
rs143062085 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016672 | GGATTTTGGTATCTG[A/C]AGGGAATCGTGGAAT | 114088 |
rs143071572 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042898 | GCCTCCTTTAACCTT[C/T]GTTCTACTCTGTTCT | 114088 |
rs143086618 | in-del | -/C | 0.113685 | 0.209567 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003706 | TGTCCCAGATTTAGA[-/C]AAATTAGCAAATGGA | 114088 |
rs143111486 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045449 | AGAGGGGCTGAGTCA[C/T]CTGACCCTGGAGGTT | 114088 |
rs143131423 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044477 | GTCCTTTAAAGGGAA[C/T]TGATTCAGATGGGTG | 114088 |
rs143161105 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085897 | AGTTCTGACAGAGAA[A/G]CAGGATGAACCCCAT | 114088 |
rs143162240 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087270 | AGGAGAAGATAGCTA[A/G]GCAGGCAGATGGGAT | 114088 |
rs143203355 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043897 | AATACATGTGCATAC[A/G]TTTAAATTATTATTA | 114088 |
rs143214473 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977108 | AGCAGGCATGACAGC[A/G]GAGGAGAGGTTGAAA | 114088 |
rs143237480 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015425 | CCCCCACCTCCATTT[A/C]CCTCTCCATTTTACA | 114088 |
rs143279574 | in-del | -/GAAGGAAG | 0.363985 | 0.222503 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066053 | TGAGCATCTCTTTTA[-/GAAGGAAG]GAAGGAAGGAAGGAA | 114088 |
rs143292182 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993585 | GTTGGTCAGGCTGGT[C/G]TCGAACTCTTGACCT | 114088 |
rs143373936 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056305 | TTTGTTTTTCAAATT[A/G]AAAAAATAAATTCAT | 114088 |
rs143445589 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029257 | GATGGGTCAAAAGGG[A/T]CACTCGAAGAGTTGG | 114088 |
rs143462492 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036320 | TTTTTTTTGAGAGCC[A/G]GTTTGTCAGCACACC | 114088 |
rs143468991 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023494 | AAATAGTAGGCAGAA[A/G]AAAACAATCAATGTG | 114088 |
rs143533873 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064310 | ATTATAATTAAATAG[C/T]AAAAATTACAAACAA | 114088 |
rs143538475 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083257 | GTTTTTTAATTAATT[A/T]ATTTATTTATTTAGA | 114088 |
rs143546026 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008827 | CTCTGCTTTCCTCTT[C/T]TTGTGTCAGCTGTTC | 114088 |
rs143564408 | snp | C/T | 0.00874735 | 0.0655527 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974885 | TGTGTGCCTGTAGTC[C/T]CAGCTACCCGGGAGG | 114088 |
rs143577023 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029564 | ATCTCTGGGTCACAT[A/T]GCTCAGCAATTACCC | 114088 |
rs143621301 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992372 | CGCTTGAGGCCGGGA[A/G]TTTGAGACCGGGCTG | 114088 |
rs143633758 | in-del | -/TTTAT | 0.244776 | 0.249945 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067860 | CCTGAAAATCTACTG[-/TTTAT]TTTATTTTGTGTTAT | 114088 |
rs143650217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982400 | TGCAAGTCCCTTCAC[C/T]TGGTGACTGGCAGAA | 114088 |
rs143694998 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992775 | AAAGGGGCAGCGTGA[C/T]GCTGAGAGTCTAATC | 114088 |
rs143707563 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009383 | GGTGAGGAACACCCC[A/G]TTAGGACTAGGGTGA | 114088 |
rs143783394 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030636 | GTGTGTGAAAGTCTA[C/T]GTGTATGTGGGTAAG | 114088 |
rs143863294 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049687 | AAAAATTAGTTGGGT[A/G]TGGTGGTGGGTGCCT | 114088 |
rs143873469 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046381 | GGAATAAAATCAGTG[C/T]ACTTTATCACTGTCA | 114088 |
rs143879883 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975686 | TAATTTGTTAGCTTT[A/C]CCATCCTATCTCTTC | 114088 |
rs143882794 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980610 | TAGTGTGATGGTTAT[A/G]TCATTATTCACTCCT | 114088 |
rs143913655 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994075 | GGATTATACTGGATT[A/C]TCCAGGTGGGCTCAA | 114088 |
rs143916241 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011143 | AACCCACTGAAACCA[C/T]TGCCTCATTTGGAGA | 114088 |
rs143917415 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083741 | AAGTGGAGATGCCAG[A/C/T]GAGCTTTAGGGTTCA | 114088 |
rs143984192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093292 | GTCCCAAAGTTTGCA[C/T]ATATAACTACTGAAA | 114088 |
rs143985473 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046752 | CCGTAAAACCCTGGG[A/C]AAATTAAAAACTCTA | 114088 |
rs144004959 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007885 | TACCAAGTACAGGAA[C/T]GCATTTAACTGCATC | 114088 |
rs144054415 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032619 | TTCAATCCTGGCTTC[C/T]TCACTTCCAGGTGGA | 114088 |
rs144080030 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026871 | GTAATACTTTGTAGT[C/T]GGGTTATTGTGAGGG | 114088 |
rs144097778 | in-del | -/AAG | 0.486067 | 0.0822953 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063481 | AAAAATTATAAATCC[-/AAG]AAGTTCACTGAACTC | 114088 |
rs144100336 | snp | C/T | 0.00019784 | 0.00994389 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998174 | GCACATTGTCTCCTT[C/T]CCCACATACACCTCC | 114088 |
rs144198372 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067139 | TGGACAAAAAACAAC[C/T]ATTAATATTTCCTCC | 114088 |
rs144217800 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070809 | AAGGTAAAAACTATT[C/T]CTGTTATTCCTGTGG | 114088 |
rs144245452 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075000 | ACAAGCAACAGGCAG[C/T]GGACATTTTTATCCA | 114088 |
rs144265847 | snp | A/G | 1.65012e-05 | 0.00287234 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998182 | TCTCCTTCCCCACAT[A/G]CACCTCCTGAGAGTC | 114088 |
rs144329658 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046102 | CTTTGGAATGACCGC[A/G]TTTTAGAAATGGAGG | 114088 |
rs144339702 | in-del | -/ATC | 0.0770498 | 0.180522 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001733 | ATTTGGATCCAAGTG[-/ATC]AGATCACAGTGATCT | 114088 |
rs144349909 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006690 | AAGACTATAATCCAG[C/T]ATTATACCAAATGGC | 114088 |
rs144367169 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990904 | GAATGAAGAATGAGG[C/T]TGTTTTCATAAATGG | 114088 |
rs144407537 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071368 | GCAACAAGAGTGAAA[C/T]TCCGTCTAAAAAAAA | 114088 |
rs144408473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090277 | TATATTGTGTTTACT[A/G]CTGACATATAGTTAA | 114088 |
rs144415384 | in-del | -/CTC | 0.0103295 | 0.0711199 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082861 | AGCTATATGTAGGTT[-/CTC]TTCTGTGCAGTAATG | 114088 |
rs144431014 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017031 | CTTTGAATTAACTGT[A/G]TGAATTAAAGGGGAA | 114088 |
rs144449803 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093583 | CAGGTCTGGCCCAGA[C/G]CCGGGCTCATCAGTA | 114088 |
rs144472537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027754 | AGGAGGGAAAAACGG[A/T]CTCATTTGGAAGAGC | 114088 |
rs144473167 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012546 | ATCTTTGTAAGTCTC[C/T]GCTTTCACTTCTTTG | 114088 |
rs144558042 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070086 | ATGGTATATTCAGTG[C/T]CATGTTTTTCATTTT | 114088 |
rs144633887 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082416 | ACAATAGGATATTAG[C/T]ACAGGATAATTAGTC | 114088 |
rs144669137 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079100 | AATCTTTTGTACATA[C/T]AGTTTCAGAAAACTT | 114088 |
rs144683791 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000431 | GGGTGGAGGAGACCA[A/T]CTTGAATGCAGGCAG | 114088 |
rs144776219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012214 | TGAAACTCTAAACCC[A/G]TTAAACAACATCCCC | 114088 |
rs144779127 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084854 | TCAAAAGAGGTAGAT[C/T]ATGTCATAGAGTAAT | 114088 |
rs144793979 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077954 | CGTTTTGGTTATGCA[A/G]TCAAACTAGAAATCT | 114088 |
rs144794716 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976581 | CCAAATCATTAAGTC[A/C]CCTGGTTTGCCTGTG | 114088 |
rs144809598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035582 | TGCTTATCTTAAAAC[C/T]GTTCCCTGGTAGTTT | 114088 |
rs144816636 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005214 | CCGCTAACCCTCTGG[A/C]AGCTTTCCCCCTATG | 114088 |
rs144893920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040675 | TCATGATGCCCTAAG[C/T]TTTTAAGAACTTGTG | 114088 |
rs144985117 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087027 | CTGGGGTGGGGGGAG[A/G]TGGCGGGCACTGCTG | 114088 |
rs144988196 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989742 | ACTATAACTCTAGGA[C/T]GGGACTGTGTTCGTA | 114088 |
rs144995702 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070102 | CATGTTTTTCATTTT[-/G]GTGCTTTTTGGTGGT | 114088 |
rs145006761 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044414 | CCTCTGCAGCTAGGA[C/T]TAGCCACTGAGATGT | 114088 |
rs145039391 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986303 | CAATGTGCCTGGGGG[C/T]AGGGAGGGAATTTTC | 114088 |
rs145039458 | snp | A/C | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026214 | CTCTCCACTGTGGTT[A/C]CTGACTTTAGGATGG | 114088 |
rs145058928 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990279 | CACCTCAGCCTCCCC[A/G]GTGTTGAGATTACAG | 114088 |
rs145099792 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091952 | GAGATTTAAAGGTTT[A/C]TTTTGGTCTTAATAG | 114088 |
rs145120152 | snp | A/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097493 | GGGATTGGAACCCGG[A/T]CACATATAAGTTTGT | 114088 |
rs145127013 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022402 | CCCCACCAGAAGCCA[A/G]CACCATGCTTTTGGA | 114088 |
rs145130943 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025653 | TTAATTAAACAATCA[C/T]TTATTGAATACATAT | 114088 |
rs145224902 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051080 | AAGGCTTTGTAGTTC[A/G]AGGTAAGGATCTTAG | 114088 |
rs145234101 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004707 | TGTGCAGCTGAGGAA[A/G]TGGAAACACAGTAAG | 114088 |
rs145246154 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052040 | GAGGGGAGGGGAGGG[A/G]AAAGAAGAGAAGAGA | 114088 |
rs145260071 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054017 | CATTAACTTTTAAAA[C/T]TGATTATCTTAAAAC | 114088 |
rs145268189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989272 | ACTCCCTGGTTTAGC[C/T]GAATCACACTTAACA | 114088 |
rs145272675 | snp | A/C | 0.0103044 | 0.0710354 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094946 | CTCCTCCATGGGGAC[A/C]GGTCTGGGAGGAGAC | 114088 |
rs145277381 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096112 | GGAGTCTCAGTGTTT[C/G]ACTCCAAACAGCATT | 114088 |
rs145285678 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995879 | TAATAGCATTTTTCT[C/T]ACTGATTTCTAAAAA | 114088 |
rs145355504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034899 | AAAAATTCTGAATAA[C/T]AATAGTACCCATCTT | 114088 |
rs145432229 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006512 | TTTCCATCGCAAGCA[A/T]CTGACAGATGAAAAT | 114088 |
rs145462594 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004422 | TCAAATTCTATCTCA[C/T]ATTTTATTTGTTTAA | 114088 |
rs145467626 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076784 | AAAGCACAGAGAGGT[C/G]AAATAACTAACCCAA | 114088 |
rs145470204 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041678 | TAAGATTAGGTGCTG[C/G]TATTGTACAATAGCA | 114088 |
rs145546322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047563 | TTGACTTACCTCTGA[C/T]GTAAATGTTCATGAT | 114088 |
rs145550600 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071324 | GAGGTTGTGCTGAGC[C/T]GAGACTGCGCCATTG | 114088 |
rs145565118 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008379 | TTACTATTTTTGTAA[C/T]TTCTTGTGTATTTCA | 114088 |
rs145590219 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075835 | TTCTGCCTTTGTTTG[A/G]TGTAAAACCCACTGA | 114088 |
rs145595769 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992007 | GGTCTCAGTGGGGAC[A/C]AAGGTTTGTGTAGAG | 114088 |
rs145604876 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002683 | CAGTGTTTAATTTTA[C/T]AGCAGTTTAGAAAAC | 114088 |
rs145632625 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022066 | ACCATCCTCTTTTCC[A/T]ACTTTTAGAATTTTT | 114088 |
rs145652782 | snp | A/G | 6.58892e-05 | 0.00573936 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022876 | TGACGCGGGCCAGCA[A/G]CTGGGCTTTTCTTCT | 114088 |
rs145665599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018737 | GCCCTCAGCATCCTC[A/G]CTGAGTAATTTTGTT | 114088 |
rs145665920 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001072 | CTTCATTGTGGCTGT[G/T]GGAGGGGAGACAGGC | 114088 |
rs145667973 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061273 | TAAAAGTTAGCTGGG[C/T]GTGGTGGTGGGCACC | 114088 |
rs145671263 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000590 | GGCCTGTCCCCAGGA[C/G]AGATGGGGAAGCCAG | 114088 |
rs145742974 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069193 | TTTCCTTTCTTAGAT[G/T]GATTCCATTTCCAGA | 114088 |
rs145781731 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 14:51073416 | AGGCTCACCAATGAC[A/G]GAATGGATAAATTGT | 114088 |
rs145816476 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055725 | CAAGACCCATGTCAG[A/G]CTTCTAGCCTACAGA | 114088 |
rs145818009 | snp | A/G | 0.163236 | 0.234461 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071253 | TGGTGGCACATGCCT[A/G]TAATCCCAGCTACTC | 114088 |
rs145849201 | snp | C/T | 9.89218e-05 | 0.00703215 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979503 | TTTTTCTATTTAAGT[C/T]GAGGAGGACCCCAAT | 114088 |
rs145938086 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977823 | TTGTGAAAAAACATG[A/G]CATTATACTATTTTA | 114088 |
rs145940794 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085641 | TTAAACATGTTTTGT[C/G]TTTTCAAAAATGGAC | 114088 |
rs145999846 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002044 | ACATAGAAATATTAG[G/T]TACTGAATAATCCCA | 114088 |
rs146015079 | snp | A/C/T | 0.00340602 | 0.0411288 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981811 | GTACCTGTTGGTGTG[A/C/T]GAGTTGTTGTGCATG | 114088 |
rs146019164 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999158 | AGGTGAAACCAATGC[C/T]GCTGGGGGAGGACCG | 114088 |
rs146043311 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070288 | ATGAATGAACAATAT[A/G]TATTAAACAAGGTAT | 114088 |
rs146051303 | in-del | -/CAGCTGC | 0.24019 | 0.249807 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058648 | ATGGCCCCAAGACCA[-/CAGCTGC]CTAGACCTCCAAGGA | 114088 |
rs146121621 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019077 | ATTTCATTAATGGCA[C/T]AATTTAGTTTAAGTG | 114088 |
rs146122049 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980372 | TGTCTTTCCCATTTT[C/T]TTGAGATCTAGCAAT | 114088 |
rs146132543 | snp | A/C | 0.000120446 | 0.0077594 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982928 | TTTGGTAACAGAATA[A/C]GGTTATTCCATACCT | 114088 |
rs146139747 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016886 | TCATGGATGCAAAAC[C/T]CATGGATATGGAGGG | 114088 |
rs146151771 | in-del | -/AAAAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088800 | TCATTGAATCAAAAA[-/AAAAC]CCGCCCCTCTATTTG | 114088 |
rs146165648 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080544 | CTTAATGTAAATAAT[-/A]AAAAAAAAGGGGTCT | 114088 |
rs146167040 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088825 | TATTTGTATTTATGG[C/T]ATCAGAATGCAGCCT | 114088 |
rs146172430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089194 | AATCCTCTGAGATCA[C/T]CTAAGTGGGTTTCTG | 114088 |
rs146236683 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037921 | CTTCAAGGGAGCACC[C/T]GTGGCTCAGCAGCAG | 114088 |
rs146241764 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994453 | GATTGGAAGATGCTA[C/T]ATGTCTGGCTTTGTA | 114088 |
rs146247862 | snp | C/T | 0.000563874 | 0.0167815 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997983 | TGGTGGGGTTACCTC[C/T]GGGCTTGCCAGCCAC | 114088 |
rs146284438 | snp | A/G | 3.29549e-05 | 0.00405911 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998123 | GGCCTTGACCCGAGC[A/G]TTGTATGTGCTGTTG | 114088 |
rs146303714 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066788 | CACTGGTTGCAGCTC[A/G]GCGTTTGCCTTATTT | 114088 |
rs146328037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087742 | AAGTTGTTATGCTAT[C/G]TTGTCCCCAGAGCAA | 114088 |
rs146379821 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983257 | GAGAAACTGCTATAA[C/T]AGGGTTAGAATGACA | 114088 |
rs146385211 | in-del | -/TGTT | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097247 | TTTCATTGTTAGATC[-/TGTT]TGTTTAGGAATTAGC | 114088 |
rs146387505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045244 | TCCTCTGAGAGGAAC[C/T]GAGATATATGGGACA | 114088 |
rs146401098 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050422 | CCATGTAAGACATGC[C/T]TTTCGCCTTCCACCA | 114088 |
rs146406269 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049584 | TGTAATCCCAGCACT[C/T]TGGGAGGCCGAGAGG | 114088 |
rs146413159 | snp | C/G | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081978 | CCTCCCTGCCCTGGG[C/G]GTCAGAGGTCAGTGG | 114088 |
rs146418760 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008034 | GTCATTTACTATATG[A/G]ATGCTTAAATCAGGA | 114088 |
rs146429199 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012897 | TTTTAAAATTGGGTG[C/T]TTTTGTTGTTGAGTT | 114088 |
rs146434492 | in-del | -/AC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999365 | TTTTACACACACACA[-/AC]ACACACACACACACA | 114088 |
rs146434565 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978467 | TTGCCCATGCAAGGC[A/C]CCTCATGCCTTAGAA | 114088 |
rs146553328 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029284 | TTGGTACAAAACAGA[G/T]GAGGCGGCAAACAAG | 114088 |
rs146591318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067281 | TTTGTACTGTAAGTA[C/T]CTTCCAAATATAAGA | 114088 |
rs146593402 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045931 | TCAATTCCATCAACA[-/G]GAAAAAAAAAGATAA | 114088 |
rs146594547 | in-del | -/T | 0.281355 | 0.248026 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083431 | GCTAATTAAAAAAAA[-/T]TTTTTTTTTTAGAGA | 114088 |
rs146612131 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004437 | ATTTTATTTGTTTAA[-/T]TTTTTTTTTTCAGTG | 114088 |
rs146623721 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976980 | AAAGAAAATATAACT[C/T]ACCTACATAAAAAAT | 114088 |
rs146654870 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043898 | ATACATGTGCATACG[G/T]TTAAATTATTATTAT | 114088 |
rs146666992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046458 | ACCACTGGGAGAAAC[C/T]GGGAAAAGTGTCGAA | 114088 |
rs146669235 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981313 | TTAGTTTAATGAATC[A/G]TAATAAGAAGAATGG | 114088 |
rs146692136 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082435 | GGATAATTAGTCATA[A/G]AAAAGAATGATGTAC | 114088 |
rs146775379 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060719 | TGATCTGCCCGCCTC[A/G]GCCTCCCAAAGTGCT | 114088 |
rs146783027 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992409 | ATAGTGAGACCCTGT[C/T]TCTACGGAAAAAAAA | 114088 |
rs146793750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995067 | ATGTTGCCCAGGCAG[A/G]ATTCAAACTCCTGGG | 114088 |
rs146824302 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055344 | TATTATAAAATGTGT[A/G]TGGTAGGTAGAATAA | 114088 |
rs146885155 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031228 | AGTTATAGCCAGGGT[A/C]CTCTGAGCCCTCTTC | 114088 |
rs146912763 | in-del | -/TTTTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077387 | TCATCTCCAATTCTG[-/TTTTTTTTTTT]TTTTTTTTTTTTTTG | 114088 |
rs146934480 | in-del | -/AG | 0.0876345 | 0.190099 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095284 | CACAGGGGGTTCGGT[-/AG]GAGTCTGAGGATAGG | 114088 |
rs146936638 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062759 | TAATCCCTGAACTGT[C/G]GATGCATGGGAGAGA | 114088 |
rs146939474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993629 | CAACATGACTGCAAG[C/T]AGTAAAGTCCTCCTT | 114088 |
rs146944901 | snp | G/T | 0.000461163 | 0.0151779 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981973 | GAGCTCCCAGTAGTG[G/T]ATGCCCTTGGAGAAG | 114088 |
rs146997433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048263 | TCTGTACAGGCTTTA[A/G]AGGCTGTGCTGATAC | 114088 |
rs147002901 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982176 | TAACATACTCCTGGG[C/T]GGGTGAGGAGCGTTG | 114088 |
rs147013044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984902 | AAGCCATAGTGCACA[G/T]AAAAACAATAAGAAA | 114088 |
rs147035348 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048629 | GTGTGTGTCTAGGGT[A/G]TCGTGTAATCAATGA | 114088 |
rs147044968 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010643 | TTTCTGGCAGTGTCT[C/G]CTGGGGATAAGGGCT | 114088 |
rs147103595 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069007 | ATAGAAGAGGGAGAT[A/G]AGTGTGGGGTGCCAG | 114088 |
rs147121790 | snp | C/T | 0.000115539 | 0.00759975 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979524 | GGACCCCAATTGTGG[C/T]CCCTTTTGTGATCCC | 114088 |
rs147134726 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023944 | TCATAAAGAACTGTG[A/T]CTTTTTATATAATAA | 114088 |
rs147176810 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064918 | AATCATTATAAATCA[C/T]AAATAAAGCTTAAGG | 114088 |
rs147177158 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019889 | ACCACTCAGTTCCAT[C/T]TTGCCTCAGAACCAG | 114088 |
rs147193330 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058739 | TCTATTACGTTTAAG[A/C]CCCTTCAATTCAGCT | 114088 |
rs147239004 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042771 | GGTGTCCCTTCTTCA[C/T]GAGCTTTGCCAGGAC | 114088 |
rs147245347 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975743 | CATGGTGAATTTCTT[A/G]GCTCACTGAAAAATA | 114088 |
rs147299319 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079949 | AGGAGTAGAGAGTGC[A/T]AGTGGTAAGATGCCA | 114088 |
rs147351076 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991419 | GGATTTTGTAAAATT[C/T]ACCCAAATATGGTCA | 114088 |
rs147368403 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988665 | TCTCTAAGTAGCTGT[C/T]AACAACAACAAAAAA | 114088 |
rs147397064 | in-del | -/C | 0.0876345 | 0.190099 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026757 | TAGAAAGAATATAGG[-/C]TTTGAAAGGGTGCAG | 114088 |
rs147411421 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024656 | GCTGGTCATTGTGTC[C/T]AGATAAAGCAATCTG | 114088 |
rs147411456 | in-del | -/A | 0.228253 | 0.249052 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043836 | CCTGTTTGGTTTAAC[-/A]TTTTTATTTTAATGC | 114088 |
rs147456469 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006166 | ACTTTAAGTAAATTT[G/T]AAAATATTTTAACTT | 114088 |
rs147472468 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045576 | CTATGATTCAAGGAA[C/T]AATGTAGCATAAATC | 114088 |
rs147472630 | snp | A/G | 0.040671 | 0.13668 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002350 | CGTGTTAGCCAAGAT[A/G]GTCTCGATCTACTGA | 114088 |
rs147515690 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043009 | GGTGGTTAATAATGT[G/T]AATAGCATAACTTGC | 114088 |
rs147528947 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072656 | GTTTCAATTTATTAC[-/T]TTTTTTTTTTTTACT | 114088 |
rs147551121 | in-del | -/AAACCC/C | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044823 | GGGCTAGATAAATAA[-/AAACCC/C]CTGCCACTCCCACCA | 114088 |
rs147605863 | snp | A/C/G | 0.0490535 | 0.14873 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054711 | CCGGAGTAGCTGGGA[A/C/G]TACAGGCGCATGCCA | 114088 |
rs147610471 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014681 | TTTATCAACTCTCTT[A/G]CTTGCTATCTTCTTC | 114088 |
rs147616033 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017744 | CACCCATATCTGGGT[A/T]GAAGCAAAGAGTACT | 114088 |
rs147653500 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051200 | ATACCCAGATAACTA[C/T]AGGAAACCTTCGTTG | 114088 |
rs147710085 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076205 | AAGACACACTCAAGA[G/T]GAAGAAGTTGAGATT | 114088 |
rs147745993 | snp | A/T | 4.94328e-05 | 0.00497131 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025284 | ATCTGCTGGACCATG[A/T]TGCGCAGCTGTACCA | 114088 |
rs147755805 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000605 | GAGATGGGGAAGCCA[A/G]CCCTGAGACTCCCTG | 114088 |
rs147815688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093670 | AGCAGCGACAGACTC[C/T]CGCCGTCCGCGCGAC | 114088 |
rs147820517 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020973 | TCCATTAAGAAGAAA[G/T]TTAAAATGTTATGGC | 114088 |
rs147830563 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984694 | CTGAAATCTTTTTAC[A/G]CTACTTTAAATACAT | 114088 |
rs147858540 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090358 | TTAATGAGATGCCAC[C/T]ATAAAGCTAAGCAGA | 114088 |
rs147859319 | in-del | -/CACAGGTGTTTTCA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025406 | GTAATCACAGGATAC[-/CACAGGTGTTTTCA]ACCAACAAGGCCAGC | 114088 |
rs147862823 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017903 | TGGGCACCCTATCCC[A/G]TACAGTCTCTCTTGT | 114088 |
rs147925399 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996299 | ATGACCCCCAGTTCT[G/T]TGACTGTGGTACCAA | 114088 |
rs147925402 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040118 | GGATAAAGTATATGC[A/G]GATAAAGTCTCTTTA | 114088 |
rs147935214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000515 | AGACTGCTCCATCCA[C/T]CTTCACGGTAGAGGG | 114088 |
rs147968629 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035744 | CGAAAAGAAAGGGTA[C/G]CATGTGCAAAAAGGA | 114088 |
rs147971685 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037089 | AAGATTTGTCCATGA[C/T]TAAGTCAAAATTAAG | 114088 |
rs148009813 | snp | A/G | 0.000247915 | 0.0111309 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982067 | GAGAGGATGATGTCC[A/G]AGTGCGCCGAGCCAG | 114088 |
rs148022505 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070154 | CCAAACACAATCCTT[A/C]AATGCTGTCTAGCAT | 114088 |
rs148029403 | snp | A/G | 0.00119737 | 0.0244387 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974895 | TAGTCCCAGCTACCC[A/G]GGAGGCTGAGGCAGG | 114088 |
rs148057036 | in-del | -/T | 0.167484 | 0.23599 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072992 | TTAATGTTTTATTTA[-/T]TTTTTTTTTTGGCAA | 114088 |
rs148065313 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980994 | ATTTTTTTTTTTTTT[-/T]CAGAGACACTAATGA | 114088 |
rs148069202 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083357 | CCTGGGCTCAAGTGA[C/T]TCTCCTGCCTCAGGA | 114088 |
rs148072689 | snp | A/G | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009177 | CCTTGGAGTGAGTGT[A/G]CCTTTACCCCACTGA | 114088 |
rs148125458 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982740 | AACTAACACGTCAGA[A/T]ATTTTGCTGGAGCAG | 114088 |
rs148164538 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023489 | AAAGCAAATAGTAGG[C/T]AGAAAAAAACAATCA | 114088 |
rs148184753 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001261 | TTGAGATGGAGTGTC[G/T]CTCTGTCGCCCAGGT | 114088 |
rs148185406 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073739 | TTACACAGGTGTGAT[A/C]AGTTTGTGGAAATTC | 114088 |
rs148190328 | snp | C/T | 0.000271573 | 0.0116496 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094448 | CTGGCACTTGAGGGC[C/T]GCGGCTTTGCTCTGC | 114088 |
rs148236873 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005227 | GGCAGCTTTCCCCCT[A/G]TGATTTATAGGGGAC | 114088 |
rs148279505 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044648 | AGGAAGAAGTAACCT[A/C]AGTCCCGGATGACAG | 114088 |
rs148319060 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052042 | GGGGAGGGGAGGGAA[A/G]AGAAGAGAAGAGAAG | 114088 |
rs148333009 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015915 | ACTATTTCAAAAAGT[C/T]CTTTCTTAAATATAA | 114088 |
rs148374671 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057109 | TATATCTGCATGGCC[A/C]CAGATGCTGTGCTCT | 114088 |
rs148383706 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019369 | TTGGCTCCCAGCATC[C/T]TATCAAACCACAGAG | 114088 |
rs148394852 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981323 | GAATCGTAATAAGAA[A/G]AATGGCTACTATTTT | 114088 |
rs148425981 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028295 | TAGAAATCATTCTCT[G/T]AAGCTTTGTCCACTT | 114088 |
rs148434418 | snp | A/T | 0.0248432 | 0.108648 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089295 | AAACATTTATCTTGT[A/T]ATAGGTTCTTCTATC | 114088 |
rs148437881 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017319 | AAGTCTGAGGCTTTG[C/T]GGTTTTAATCGAGAA | 114088 |
rs148496371 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039025 | TCTCAAAGGCACGGG[G/T]TCATTAGAAATGCCT | 114088 |
rs148547613 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043074 | TGTTTCTTCCTCTGA[A/G]TTTCTAAGAATGTTG | 114088 |
rs148553005 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976594 | TCCCCTGGTTTGCCT[A/G]TGTCTTAGAGACTTT | 114088 |
rs148590109 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084976 | AAGACCTGCTCTAGA[C/T]AGAAAGTGTTTAATT | 114088 |
rs148593514 | in-del | -/GGG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048268 | CAGGCTTTAGAGGCT[-/GGG]GTGCTGATACCATGT | 114088 |
rs148633050 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093475 | AGGCCCAAGCCTGCA[C/T]GTCGCGTTGCCATGG | 114088 |
rs148636788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064971 | CTCTGACTGGCTCCT[C/T]ACTTTGGGCCACTGC | 114088 |
rs148641553 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049954 | GGGTTGGGTGCATTA[A/T]GAGTGGAAAGAAAGG | 114088 |
rs148647213 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984088 | ATCTCCCTTCCTTAA[C/G]ATTTGGATACCTGTA | 114088 |
rs148666748 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994136 | GTAGGGGCTACATGG[G/T]GGCTCATGCCTGTCA | 114088 |
rs148688971 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999334 | CAAAGTCAGGAATGA[A/G]AAACTGACAAATAGG | 114088 |
rs148689375 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025656 | ATTAAACAATCATTT[A/G]TTGAATACATATTTG | 114088 |
rs148706473 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075177 | GGGTCGCCCAAGGAG[C/G]TAGGCACAGGATCCA | 114088 |
rs148709089 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002324 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT | 114088 |
rs148719068 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985594 | CAGAAGGGCTGCAAA[-/C]CCTCCACATTACTGC | 114088 |
rs148748514 | snp | A/G | 9.88973e-05 | 0.00703128 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009125 | TGGATTGCAGCAGAG[A/G]GCTGTTGTCCAGACT | 114088 |
rs148758277 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006841 | AGACTTGAACAGACT[A/G]GACAAACAGCCTTGT | 114088 |
rs148801618 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046232 | ATAGGGCAACGCAAG[A/G]GACACTTGTGGGGCT | 114088 |
rs148865211 | snp | A/C | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008403 | TATTTCAAAAGAAAC[A/C]GTTAAAAAGAAATAT | 114088 |
rs148907856 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021141 | TTTGGGTTTCTGAAG[A/C/G]GTGCTCAGATTGAAG | 114088 |
rs148949704 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030460 | GCAGATGCCAATTTA[C/T]CTCTAAGCCCAGCAA | 114088 |
rs149012975 | snp | C/T | 1.64939e-05 | 0.0028717 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979513 | TAAGTCGAGGAGGAC[C/T]CCAATTGTGGCCCCT | 114088 |
rs149022228 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040890 | ACAACCTTATTCTAA[C/T]ATCTGATCATTTTCA | 114088 |
rs149075454 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977656 | GCCTTGGTTTTCAGA[C/T]AGAGGAGCCTACTGG | 114088 |
rs149097028 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044420 | CAGCTAGGATTAGCC[A/C]CTGAGATGTAGATGA | 114088 |
rs149111943 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087206 | TGGGGGAGGGCAAGC[A/G]TAGTGGACAGGAAGG | 114088 |
rs149120253 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989922 | AAAAGCAATCAAGAA[G/T]CAACAAAGCAAAGAT | 114088 |
rs149159278 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067584 | ACCTCCCACTTTGCT[A/G]TAGCCCACTGGGCTT | 114088 |
rs149164487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995930 | TATTTGATCCTATAG[A/G]CTTTGTCTATTGTTA | 114088 |
rs149165945 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051632 | ATAAATCACCCTAAA[C/T]TGAGATTGATAGTGA | 114088 |
rs149217157 | snp | C/T | 1.65091e-05 | 0.00287303 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000684 | GGCTGTCTACTGACC[C/T]GGAATTGACCACCGT | 114088 |
rs149261575 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070071 | ACAAGTGTACTTTTC[A/G]TGGTATATTCAGTGT | 114088 |
rs149267549 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997924 | ACAGCGGCTCTGTGC[A/G]GAATGCAGAGCAAGT | 114088 |
rs149319343 | snp | A/G | 0.030278 | 0.119257 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002247 | CTGTCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 114088 |
rs149340182 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982270 | TCCTGGGAGTTGGTA[C/T]TCTCTGCACCAGAAG | 114088 |
rs149358576 | in-del | -/ATTAGTA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031909 | ATACTAAACAAATCT[-/ATTAGTA]CACCATTTGTATTGT | 114088 |
rs149417346 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011964 | CTTAATTTGCTTAAT[A/C]ATTCCTGTTCTCTTA | 114088 |
rs149426806 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062695 | CCAGCTGGAAATTGA[C/G]AGGGGAATCCTTGAA | 114088 |
rs149454506 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093213 | TGTTGCTAAAGCCTC[C/T]TCGTGTCTAGCCATG | 114088 |
rs149479347 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032614 | CTCAGTTCAATCCTG[A/G]CTTCCTCACTTCCAG | 114088 |
rs149527864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038331 | GACTTCTGACCTACA[A/G]GAGTGCAAGGTAAAA | 114088 |
rs149573250 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015379 | AATTAGGAGAATTTC[A/G]TGCTTAACCCAACCA | 114088 |
rs149604776 | in-del | -/AAGT | 0.445724 | 0.155538 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064508 | AGAATCAAAAGTTAA[-/AAGT]AAGGGGAAGAAAAAG | 114088 |
rs149624891 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979934 | GACTAGGAAAAAGTC[A/G]CCTTTGGGCTATCAG | 114088 |
rs149626673 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046038 | GAAAATATAATGTTC[A/G]TTGGAAAAAAAAGCA | 114088 |
rs149643057 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088750 | CTACCTAGTGGTGAA[A/T]GGGTAGATAACATTG | 114088 |
rs149646940 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990806 | AGAATTGTACAGTGT[C/T]AAAGATGAGTTTCAA | 114088 |
rs149678574 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016976 | AGGAGGGAGTTTCTA[C/T]GTGTCCCATTGTGTC | 114088 |
rs149694788 | snp | A/G | 0.138546 | 0.223781 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053670 | GTTACATATGTATAC[A/G]TGTGCCATGTTGGTG | 114088 |
rs149716360 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059977 | AAAATATGATACAAA[C/T]TGTTTCTTAAAAAAG | 114088 |
rs149727516 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047519 | TTATAAAGTTAGAAA[C/T]CAAGAGAGGACACTC | 114088 |
rs149746007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991863 | TGTGGAGGGATACAA[C/T]AGAGACTCAGGTAGG | 114088 |
rs149786009 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071059 | GTGGACTGATGGGGA[C/T]GACAAAATAAGAATC | 114088 |
rs149794470 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976282 | ACATTTCTGGTGCTA[C/T]GGCCAGAATGTGTGG | 114088 |
rs149844607 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003861 | AGTGATGTTGTATAT[A/G]AAAGGTGAATGTGCC | 114088 |
rs149887818 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081817 | GCCAAATGGCAGAGA[C/T]GCATGGAGTAAGGTA | 114088 |
rs149891081 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984006 | ACCTGAGGGAGGGGA[A/G]GAGGGATGGTAGGAG | 114088 |
rs149907413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019733 | GCTTTGCAATGCCCT[A/G]TGAGGTACCACTTCC | 114088 |
rs149959176 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025535 | ACTCCCTGTGCTCCT[C/G]AGTAGTTTCTCCTTG | 114088 |
rs149985285 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047960 | GTGAGACCCTGTCTC[-/AA]AAAAAAAAAAAAATC | 114088 |
rs150002880 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033625 | CATCCTTGGCCATAC[A/G]GCTTGCTTTTCAGCC | 114088 |
rs150012732 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995655 | TTTACCTTTCTGTGA[C/T]ACAGAATTTTTGTTT | 114088 |
rs150078456 | in-del | -/CAGAGCTCATAATCTCAAAT | 0.0566069 | 0.158427 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056482 | CTATACTCTAGATCC[-/CAGAGCTCATAATCTCAAAT]ATAAAACCTGACATT | 114088 |
rs150085086 | snp | A/T | 0.021333 | 0.101051 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997570 | CTCTAGCACCCCACC[A/T]CCCATTTGAAACACA | 114088 |
rs150101900 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037323 | AAACCCAAGTGCAAC[A/T]TGGTTCCCACTAGGA | 114088 |
rs150106447 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008363 | AGATGAACAAAACTT[A/C]TTACTATTTTTGTAA | 114088 |
rs150156813 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042218 | GACAGAAATCCCTCA[A/G]GACCCAGCCTGTCGT | 114088 |
rs150202550 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018114 | CTAATTTTTCCAAAT[C/G]TCTTCATTGTAATGG | 114088 |
rs150295623 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032361 | AATATTCTCTCAAAG[A/G]CTATGCATCCTTCTC | 114088 |
rs150313484 | snp | A/C/G | 0.0178166 | 0.092742 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074106 | AATGATCATAACAAC[A/C/G]AAACCAAACATCTGC | 114088 |
rs150313884 | snp | C/T | 0.000331425 | 0.0128687 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977377 | TGAGACTGTGAGTCC[C/T]GAGAGGCATCGTGCA | 114088 |
rs150357335 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014651 | AAGAGTATAAATACT[C/T]TCTCTCTAGTTGTCT | 114088 |
rs150396769 | snp | C/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095939 | TGAACGTGCTTCCTT[C/G]CACGGATCCTTCTTC | 114088 |
rs150406914 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051325 | AAGAGAGCAAGGAAG[A/G]AAGAGATGAGACAAA | 114088 |
rs150407994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083663 | CTTGGAGTTACAAAA[C/T]GGAGAGAGATGGTGA | 114088 |
rs150455244 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026788 | ATTCTCGCTCTATCC[C/T]CTATAAGTGTGACCT | 114088 |
rs150465475 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990655 | GTATACTAATCCAGT[G/T]CCCTCTGTGTCCTGG | 114088 |
rs150513759 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987879 | CGATCTCAGCTCACT[A/G]CAACCTTTGCTTCCT | 114088 |
rs150514863 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052828 | ACTGGTGCACTATAC[A/G]AGCCCCATACCTCAT | 114088 |
rs150514938 | snp | A/G | 1.66835e-05 | 0.00288816 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982089 | CCGAGCCAGGGTCGA[A/G]AGCAAACCAGGCCAC | 114088 |
rs150555941 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028714 | TTTCTAGGTTACTGA[A/G]AAGGTGTCACGATCT | 114088 |
rs150565779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991823 | TCCAGAGAGGCTAAG[A/G]GACATATCCAAGTTA | 114088 |
rs150611087 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070907 | TTTCTTTCTTTCTTT[C/G]TTTTTTTGGTGGAGA | 114088 |
rs150630552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011222 | TAAATAGGCATCTCT[C/T]TGAGCAAGCGGTTTC | 114088 |
rs150672961 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049550 | TATATAATATAGGCC[A/G]GGCGCAGTGGCTCAT | 114088 |
rs150713331 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058235 | CATGGAACTCAGATC[A/C]AAAACCTAAGTTCAT | 114088 |
rs150722871 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019566 | GGATAATAACACCAG[C/T]GTATGAGCTAATTCT | 114088 |
rs150766901 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065455 | GGGCAGTCACAATAT[A/G]TCATCTTCCAGCCAA | 114088 |
rs150771974 | in-del | -/T | 0.17654 | 0.238964 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062124 | TTTATGATATTGTGC[-/T]TTTTCATTTCTAGTA | 114088 |
rs150784819 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005401 | AAAGGCTTGGTGAAC[C/T]GTTAGGTCATTGTTT | 114088 |
rs150820906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033371 | GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCT | 114088 |
rs150839127 | snp | C/T | 1.691e-05 | 0.0029077 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979575 | AGAGAAAAATTGGGG[C/T]TCATTTCCTTGTGGT | 114088 |
rs150863479 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075494 | ATTAAAAATATCTCT[A/G]GGACATTTACAATCC | 114088 |
rs150884250 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088639 | TACATGGAGTAATTT[C/T]GAGTTGGTAAAAAAA | 114088 |
rs150965553 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077646 | TGATCTGCCTGCCTC[A/G]GCCTCCCAAAGTGCT | 114088 |
rs150968752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981516 | GTGTTTCAGCATCCT[A/G]GATTGTTTTCTTATA | 114088 |
rs150970644 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047193 | TTTTAACATTCTGTC[C/G]CTTTTTTCCTAGAAT | 114088 |
rs150985543 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089401 | TGCAATTTATCATAC[C/T]GATGGTAAGGACAAA | 114088 |
rs151020356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985285 | CTCAGATCTTTGGTC[A/G]TTAGGCATTAGGAGT | 114088 |
rs151031216 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999843 | GGAGAGGATGGATGA[C/G]AATGAAGCTCTGTAT | 114088 |
rs151038689 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054958 | CCTCAGCCTCCTGAG[C/T]AGCTGGGACAACAAG | 114088 |
rs151042288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990078 | CTAGAGTGTAGTGGT[A/G]TTGATCATAGCTCAC | 114088 |
rs151046911 | in-del | -/G | 0.21695 | 0.247806 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083650 | AGAGAAGGAAATCTT[-/G]GGAGTTACAAAATGG | 114088 |
rs151081210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030684 | GTGTAAGTATGTAAG[A/G]ATGTGTATGTGTATG | 114088 |
rs151083764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002845 | ACTAAATCAAACATA[C/G]CTAAATCAAAATTAG | 114088 |
rs151091519 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993086 | GACCTCATTTGGTAG[C/T]AACTTTCATTTGGTA | 114088 |
rs151127324 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043736 | TCTCTAGCAGCAGAA[C/T]GAAACTGAGAAGAGC | 114088 |
rs151170428 | in-del | -/TGGCAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012252 | CTTCCTCCCAGCCCC[-/TGGCAA]CCGCCATTCTACTTC | 114088 |
rs151179441 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014148 | GATTCAGTTCAATGA[C/T]GCATTCATGTACTGA | 114088 |
rs151195993 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050936 | CAACTGGTATCTGAA[C/T]GCAACCTCACGGGAG | 114088 |
rs151248279 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021412 | TGCAAGTAATTTTGC[C/T]CTGTCAAACTTCTAT | 114088 |
rs151300922 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026323 | CTGATGGCATCTTTG[A/G]GCAGCTGAGTCAACA | 114088 |
rs180701248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984605 | CTTGGAAATAAGTTT[A/G]TAGAATCTGAATAGG | 114088 |
rs180704451 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975835 | TAATGAATTTCAAGG[G/T]TAACCTATGTAAGTC | 114088 |
rs180716598 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006408 | ACAACAGGAAGAGTT[A/G]TGTATATATTAACAG | 114088 |
rs180719600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026967 | TGCCAGTTACTGGCT[A/G]TTCAACCCTTTATAC | 114088 |
rs180787077 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080650 | AGATCCAGTGTCCCA[A/G]TTCTATCCATTTATA | 114088 |
rs180790035 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059178 | AAACAGTGAAACACC[A/G]ATCAGAAAACAGAGG | 114088 |
rs180798177 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037733 | TTTTTTTTCAAGAAC[A/T]TGAAAGCAACTCCTG | 114088 |
rs180800441 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089714 | ATTCAACTGAATATT[A/C]TCTCTGGACCCATGA | 114088 |
rs180811461 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048679 | CTTTGGGTGAGGTGG[C/T]TTAACAAAACATCCC | 114088 |
rs180827451 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070888 | GACTCACATTCCTAG[A/G]CGTTTTCTTTCTTTC | 114088 |
rs180834153 | snp | A/G | 0.000399281 | 0.0141238 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998156 | GTGAAGACCATCCAC[A/G]GTGCACATTGTCTCC | 114088 |
rs180845463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019701 | ACAGTTAATATACAT[C/T]AAAGATTGTGCTAAG | 114088 |
rs180963092 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002355 | TAGCCAAGATGGTCT[C/T]GATCTACTGACCTCA | 114088 |
rs180975792 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023179 | TATCACTTAAATTTA[A/T]CAAAAGGAAATCATC | 114088 |
rs180982015 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992182 | GTGTTCCCTGTAGTT[A/G]TTCTTCTGACAGGTT | 114088 |
rs181016644 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083653 | AGAAGGAAATCTTGG[A/C]GTTACAAAATGGAGA | 114088 |
rs181023060 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014592 | ATTTAGCAAGATTTC[C/T]CACATTATAGAAATC | 114088 |
rs181036059 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033434 | TTAAAATATACATAC[A/G]TAAATCACGAAAACA | 114088 |
rs181042581 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054171 | GGCTCAAACCATCCT[C/T]CCACCTCAGTCTCCC | 114088 |
rs181050050 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064405 | TTAAATTCAAAAGTG[A/T]AACTACTCCAATTAA | 114088 |
rs181057831 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040845 | CTCTTCCGCTTACTA[C/G]CACTGCTTCAATTAT | 114088 |
rs181087785 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979978 | GGAATATTGCACACT[C/T]TGTATAAATGGTGTG | 114088 |
rs181130737 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090663 | GTGCAGTGGTGAGAT[A/C]CTGGCTCACTGCAAC | 114088 |
rs181211696 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022572 | GTCCCATGAAGGCAA[G/T]AATTTTGATTTCTTT | 114088 |
rs181213432 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053734 | GTATATCTCCCAATG[C/T]TATCCCTCCCCGCTC | 114088 |
rs181248424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990859 | AATAATTTGCTTTTG[C/T]TGGGAAGATTTTAAA | 114088 |
rs181254473 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013080 | GCTTTTGGTGTCATA[C/T]CTGAGAAATCATTGC | 114088 |
rs181260075 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031651 | TGATGTACTCTTTTC[A/C]CTGTTGCAATTGTAT | 114088 |
rs181346251 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981053 | TAAGGTGGACCAGGG[A/T]CCACAGTAGAAATTT | 114088 |
rs181352013 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064560 | GAAATCAATGAAATT[C/G]AGAATAACAGAAATA | 114088 |
rs181356892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023792 | TAATTTACAGTAAAC[A/G]AAAGCTAAATACTCA | 114088 |
rs181464554 | snp | C/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096294 | GAGGGAGGAAGGAAG[C/G]GGGGGGGAAAGGAAA | 114088 |
rs181466915 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042884 | ACACAACCTCCCCTG[A/C]CTCCTTTAACCTTCG | 114088 |
rs181469025 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084395 | TAGTTCCATCAATGA[C/T]AGATTCACTTCCATA | 114088 |
rs181471612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076519 | ATCTGTATAGATACA[C/T]AATCATAGTAAAAAC | 114088 |
rs181477260 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002423 | AGAGATATGAGCCAC[C/T]GTGCCCGGCTGGGAA | 114088 |
rs181482708 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053911 | TTATGGGTAAGAGTG[A/C]ATCTACAATGGTTTT | 114088 |
rs181493463 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042190 | TGGTTTTTCAAAGCC[A/G]TTGCAAGTATGTGAC | 114088 |
rs181511350 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014018 | TGACATCTGCCCTTG[A/G]CTACAGGTACTGGAA | 114088 |
rs181627354 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084979 | ACCTGCTCTAGACAG[A/G]AAGTGTTTAATTCCC | 114088 |
rs181629574 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985559 | GATCCAGTCTCCCAG[A/G]CACTGCTGGTTTCCT | 114088 |
rs181633691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991698 | TCATAGCATTTTCTG[A/T]AACAACTTTCAACAG | 114088 |
rs181635410 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006724 | TTAGGTTAACTTCAT[G/T]AATCATTGTTCTGTT | 114088 |
rs181640299 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027732 | TTTCCAGGAGCCCAA[C/G]GGATAAAGGAGGGAA | 114088 |
rs181680014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049047 | GAACATAGTTTAGTG[C/T]AAGCACCGTTATGTG | 114088 |
rs181737738 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066099 | GGAAGGAGGGAGGGA[A/G]GGACGGAGGGAGGGA | 114088 |
rs181777467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033052 | TGGTCCTAATCATTC[C/T]GGATAAGAGATAATC | 114088 |
rs181883411 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029098 | GTGCCCAGGCAGAAG[A/C]CAGTATCTTCTTTCC | 114088 |
rs181922537 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091035 | AATCACTTTTTTGGT[A/G]TTATAATTCTTTTAA | 114088 |
rs181943803 | snp | A/C | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071660 | ATAAAAAAAAAATTA[A/C]CCAGGCGTGGTGGTG | 114088 |
rs181949524 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049593 | AGCACTTTGGGAGGC[C/T]GAGAGGGGTGGATCA | 114088 |
rs181954509 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077064 | AAGCCCTTTCTGCCA[G/T]GCTCATTCTATTTCC | 114088 |
rs181972423 | snp | A/T | 0.00199481 | 0.0315187 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975307 | ACATCAGAAATGACA[A/T]TTTTTTCTAGTATAG | 114088 |
rs181978056 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997009 | AAGTGGGAAAAAAAA[C/T]ACCACCATAGTTCTT | 114088 |
rs182118477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022460 | AATATAATTCTATTA[C/T]TTATAATCACCCAGT | 114088 |
rs182126306 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058607 | CCACTGGGGTGGTGC[A/G]CTGGTGAGCCACCCT | 114088 |
rs182180875 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082492 | TTTAAAAACATTATG[C/T]GAAGTAAAAGAAGAC | 114088 |
rs182189199 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062831 | AATAAATAAGCAGAG[A/G]TATCTGCATCTGCCA | 114088 |
rs182198299 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038781 | CTTCTCCGTCAGTCT[A/G]GAATCAACTACTAAG | 114088 |
rs182199840 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000438 | GGAGACCAACTTGAA[A/T]GCAGGCAGTCTGACT | 114088 |
rs182204083 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018173 | ACAGGGATTGAGGTG[A/G]TTCTTGGCTTGAATT | 114088 |
rs182212176 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985998 | AATGCAAGCTCAGCT[G/T]GTGGGGTGAGGATCG | 114088 |
rs182224706 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097277 | TAGCTAAATCAGTCA[A/C]TCCTAGGAGAGCTCT | 114088 |
rs182405500 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036692 | TTTCTCAAGTATTTT[C/T]GATCCAGTGTTGGTT | 114088 |
rs182472700 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050418 | GCCACCATGTAAGAC[A/G]TGCCTTTCGCCTTCC | 114088 |
rs182482714 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007300 | AGAGGCTGATCCAGG[A/G]GGATTTATCTGGGGC | 114088 |
rs182503594 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092649 | CCCCAACTAAATGGA[C/T]CATTTAAAAAATGAA | 114088 |
rs182510608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072965 | CACAAGGAAAAGGCA[A/G]CTTATTTCAGAATTA | 114088 |
rs182517279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051380 | TCCCTCTCTCTTTGG[C/T]CTGCCCAAGGACCCT | 114088 |
rs182545380 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010960 | ACCATCTGAACCCAG[C/T]TCCTTTCCCTTCCTG | 114088 |
rs182553780 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029824 | AGCTGGAACACAAAC[C/T]CTCATCTGATGGCAA | 114088 |
rs182560293 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977929 | CTGTCTTCTCCAGCC[C/G]AAGAGTCTTTATCAA | 114088 |
rs182564966 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091979 | ATAGATCAAGGATAG[A/G]CTTGTCATAAAAAAA | 114088 |
rs182686657 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015345 | TCATGTGACACAACC[A/C]GAAGCAAGACCTGAG | 114088 |
rs182715972 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003887 | GTGCCAAAATTACAG[C/G]CTCATTAGCAGAAAC | 114088 |
rs182730772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077675 | CTGGGATTACAGGCA[C/T]GAGTCACCACTCCCG | 114088 |
rs182742308 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055074 | TGATCCGTCCGCCTC[C/G]GCCTCCCAAAGTGCT | 114088 |
rs182749885 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033689 | TGCTCTTCCTCTTTG[A/T]CACAAGAATCAGTGG | 114088 |
rs182762260 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993306 | AGAGTTTGGATATTA[C/T]GCTGGAAATGATGGC | 114088 |
rs182806223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081260 | AGATTCTCAACATCA[C/T]TAGTCATTAGGGAAA | 114088 |
rs182812254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986824 | TCTTTGTTTCTCTAA[C/T]GATAAACAGACTGTA | 114088 |
rs182837905 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029256 | GGATGGGTCAAAAGG[A/G]TCACTCGAAGAGTTG | 114088 |
rs182852744 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072396 | CTACTTTCTTGCATA[C/G]AATCAGTTATGGATT | 114088 |
rs182858190 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003474 | GATCACAGATGGTTT[C/G]AACTTAAATCATGCA | 114088 |
rs182865085 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024262 | CTGCACATTTTATGC[C/T]AGCAGAGTAAAGAAA | 114088 |
rs182982471 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983069 | AGTACCCCAAAAGGA[C/T]TCAATTTAAAATGCC | 114088 |
rs183019962 | snp | A/G | 0.000122782 | 0.00783429 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983447 | ATACTACACATCAAC[A/G]CTATGAAACAACAAC | 114088 |
rs183028789 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078220 | GAGATAAAAGAACAG[A/T]AGGACAGGAAGGAAT | 114088 |
rs183040223 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025887 | ACTCCTGCCTCATCC[A/G]TGTCCTCTTCCTTCT | 114088 |
rs183084086 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086172 | TGTGCTTTATAGGTA[A/T]GCTTCCTGGGCTTAT | 114088 |
rs183089419 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066926 | CAGTTAGTTTACATA[C/T]TAAATTAGTCTGCAG | 114088 |
rs183094140 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043229 | AACTGGAGTTATGTA[C/T]AAAAAGAAGAGAGGA | 114088 |
rs183105511 | snp | C/T | 1.65097e-05 | 0.00287308 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025232 | TTACGTATTAACCGG[C/T]GGGTTTCCTTGCGTC | 114088 |
rs183115110 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060432 | CACTCCACATAATGT[A/T]TTTGAGACTCATTCT | 114088 |
rs183126663 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016363 | GGAGCAGGAACCCTA[C/T]TGTGAACTGCGCATG | 114088 |
rs183149944 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068734 | TATGTAGAATTAGAA[A/G]AGGAGGTGTGATGAG | 114088 |
rs183165694 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988040 | TCCTGAGCTCAAAGC[A/G]ATCTGCCTGCCCCAG | 114088 |
rs183236559 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977196 | CTTCTCCCACTCCTG[C/T]CAACTCTGCACCCCA | 114088 |
rs183244116 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000127 | ATAACAGGAGACCAT[G/T]TCAATTAAGAGGAAT | 114088 |
rs183264199 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022247 | GCCTTCATGAATGGA[C/T]GAATGCTATTATCTT | 114088 |
rs183294720 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004629 | GTTGTGAGAGGTTTA[C/T]AGGTATTCACTCATT | 114088 |
rs183323268 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044858 | CTATCATCTCCACTA[A/G]GTGAGAGTTTCTGTC | 114088 |
rs183341232 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038599 | GAATCTGGCCCACTA[C/G]AACAATGTGAACACA | 114088 |
rs183406995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088326 | ACATTGAATCAAGTG[G/T]CTTTGTTTGTTGCAG | 114088 |
rs183422173 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016165 | AATCATCTCTAGATT[A/G]TTTGTAATACCTAAT | 114088 |
rs183428078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056441 | TAAGCAAATTTATCA[C/T]GAAATAATCCCCAGT | 114088 |
rs183547914 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990004 | CTGTTTGGCCACCAT[A/G]TATTTCTTTTGTTTC | 114088 |
rs183562257 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011950 | ATTGAGTGGGTAATC[C/T]TAATTTGCTTAATCA | 114088 |
rs183570940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035139 | ATAAATGTATGAGAT[A/G]TTTCAAAGGATACAC | 114088 |
rs183573411 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998929 | CTTAATATGACAACT[A/C]TCTGGTAGGATACTA | 114088 |
rs183588513 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038389 | TTTTTGTACTGTTTC[A/G]TGGCAGCAATAGAAA | 114088 |
rs183642514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078791 | ATTCAACGGAGGAGA[C/T]ACGTAGGATAAACAG | 114088 |
rs183650920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995187 | GCATGTTCTTTATAA[A/T]TTCCATTGAATTTAA | 114088 |
rs183657847 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035546 | TAAAGAACTGAAAAT[A/C]ATTGGATCTCAAAAC | 114088 |
rs183785200 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976606 | CCTGTGTCTTAGAGA[C/T]TTTCCAATTTTATAC | 114088 |
rs183804994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021193 | GCAATGTTAGGCCAG[A/G]TGCTGGATACAGAAA | 114088 |
rs183807125 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032367 | CTCTCAAAGACTATG[A/C]ATCCTTCTCCCAGCT | 114088 |
rs183833188 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064426 | CTCCAATTAAAAGGT[A/G]AAGACTAGCAGACGG | 114088 |
rs183865964 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095642 | AGGCTTCTGCACGGC[A/G]GTGGGGCTTTTCTCC | 114088 |
rs183867980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075525 | AATCTAGTTTACACA[A/T]AGTTTTCGGGAACTC | 114088 |
rs183868478 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057079 | TTTGGGTAGCCAGCA[C/T]AGGCTCTCAGACATT | 114088 |
rs183877061 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991175 | TATCATCAGAGGAAC[G/T]GAAAATTCCTGTATT | 114088 |
rs183878483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053857 | AATTACAAATTATTG[C/T]CCAAAGTAAAGACTA | 114088 |
rs183885986 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013383 | TTCTATTACAGTGGT[C/G]TATATATCTGTCTTT | 114088 |
rs183943528 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061099 | TGAAGTGTCTGCTCG[A/C]GTATTTTGTCATTTT | 114088 |
rs184021710 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996362 | TTAGACACCATAATC[C/T]TATGAACATTAAAAT | 114088 |
rs184029094 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017486 | TATGCAAAGCATGCT[C/T]TTAATGTATAGAATA | 114088 |
rs184104849 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081899 | ACCTCCACGTGTTCT[C/G]TAACCTGGAAACTTT | 114088 |
rs184105528 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079729 | TCAGGCTGGAGGTAA[A/T]GGGTACACACACCAG | 114088 |
rs184109357 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057989 | TAAATTAAATTCTAA[C/T]AAACCCGATTATTTA | 114088 |
rs184117617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035689 | GTAGAGAAAACAGCT[C/T]TCTGGAAAAAGGACT | 114088 |
rs184316375 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052799 | AGTTAGAGTTTGGTA[A/G]GTCTCCTCACTTTAC | 114088 |
rs184393951 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031070 | GGAAAATCGCTTGAA[C/T]CTGAGAGGCGGAGGT | 114088 |
rs184430138 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075030 | AAAGAGACTCTTGTC[A/G]GGAACTGAGTCAGAG | 114088 |
rs184444348 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005096 | CTGGAAAGCTATTAC[C/T]GGTACACTGTTAAAG | 114088 |
rs184505916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069383 | CACAACTCAGAGGTG[A/G]GTGGTGTGGTGTAGG | 114088 |
rs184513207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045557 | TCCCTTCCAACTGGA[C/T]GTCCTATGATTCAAG | 114088 |
rs184532696 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983651 | CCTCCTCCAATTGAT[C/T]CTAAACTCTGTAGCT | 114088 |
rs184559030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039215 | GGAACATCTAGACCC[C/T]CACATGTTGCTACTG | 114088 |
rs184574030 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995869 | AAAACTCTGTTAATA[A/G]CATTTTTCTCACTGA | 114088 |
rs184618668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001766 | CCGTTTCAAAACTTC[C/T]GAGGAACCTGATGTC | 114088 |
rs184639596 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083261 | TTTAATTAATTAATT[A/T]ATTTATTTAGAGACA | 114088 |
rs184681680 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063556 | TATGACAGTCAAAGT[C/T]CTAAAAACCAAAGAT | 114088 |
rs184749008 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978910 | CTAAGTTGTAGGTAG[A/G]GACTATGTTTTCTAC | 114088 |
rs184772238 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022594 | GATTTCTTTATTATT[C/T]CTATGTCCATTGCAG | 114088 |
rs184793604 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089607 | CTGAAAAAAACGGAG[C/G]CTTATCAGCTATTTC | 114088 |
rs184794766 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070239 | GCATCGTTCAAGCAT[A/G]AGTTATAGTGCGATG | 114088 |
rs184811951 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046899 | AATGCCAGGAAAACC[A/G]TTGGCTCTTATTATA | 114088 |
rs184887117 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071034 | AATACATTTACATTT[C/T]GGGGTTTTGGTGGAC | 114088 |
rs184947778 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027101 | CTGGTGCACAGTGCA[C/T]GATGCGTGCTTAATA | 114088 |
rs184951705 | snp | C/T | 0.000938847 | 0.0216458 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979307 | CAGCTTCCCTCTCTT[C/T]GGTTGGATTGAACGG | 114088 |
rs184988677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090255 | TTTACCACAGGAATA[C/T]ATAGACTATATTGTG | 114088 |
rs185003795 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048744 | AATCCCAGCACTTTG[A/G]AAGGCCGAGGCAGGC | 114088 |
rs185033868 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063916 | AAGACCATCTGAAAT[A/G]GGCATAAATACATAT | 114088 |
rs185041757 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040536 | TGACTGGAGCCCTGG[A/G]GTGAGGGATTGGACA | 114088 |
rs185048167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006561 | GGCTAGGCTCTCACT[A/G]AATTAATTAAACTCA | 114088 |
rs185050661 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074402 | ACTGTCTTCCCCCAA[G/T]AAGTTTAGCACCAAA | 114088 |
rs185073176 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022737 | CTGTGGGCATCCTCT[C/T]CTCCTGTCCATGGGA | 114088 |
rs185076903 | snp | C/T | 0.00159617 | 0.0282053 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974918 | GAGGCAGGAGAATTG[C/T]TTGAACCCAGGAGGG | 114088 |
rs185098936 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017623 | GTGGGTTGCAATAAG[A/C]GTGAAGCAGTATGAT | 114088 |
rs185126035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058363 | CCTACTCTAACGACA[C/T]TCTTGGTTGGGAAGC | 114088 |
rs185128051 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088957 | CTTGGTTGCAAGTGG[C/G]AGGAAACCAACACAA | 114088 |
rs185206391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996486 | ATTCCCATGATGTAT[C/T]ATGAATAGAAATAGT | 114088 |
rs185247153 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036408 | TTGTTTTAGGCTTTT[A/G]GCAGCTTGAAGCCAT | 114088 |
rs185265721 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041686 | GGTGCTGCTATTGTA[A/C]AATAGCACTCTTTTC | 114088 |
rs185273829 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981661 | CTCAGCTGAGGCTCA[C/T]AGATTGCCTGTGCTA | 114088 |
rs185332801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080004 | GAATGGGGAGAGGAG[C/G]ATTTTGCCTCATCCC | 114088 |
rs185369345 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014634 | CTTAAATCAGATCTT[G/T]TAAGAGTATAAATAC | 114088 |
rs185439836 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005802 | AATACAACCAGAAAA[A/C/T]GTGCCATTACAATTT | 114088 |
rs185559946 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984121 | CCATGAGAAATTACA[C/T]TGTGTGGAGGAAGAC | 114088 |
rs185561740 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034750 | ACTTACACTACAGTT[G/T]AGCAGTTAATAGCAT | 114088 |
rs185579907 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026754 | ATGGTAGAAAGAATA[C/T]AGGTTTGAAAGGGTG | 114088 |
rs185580966 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988696 | ATCCTACCTTGCAAT[A/G]AGAACTTTTCAAATG | 114088 |
rs185597930 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030583 | GTGTATGAGTGTGCA[A/T]ATGGTGTGTGTGTGT | 114088 |
rs185621369 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985326 | TAATTCGGCTAGCAG[C/T]GATCCCACCCCATTG | 114088 |
rs185646213 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077981 | ATCTCCCTCACTGTG[C/T]GAACGACCCAATTGA | 114088 |
rs185653964 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055587 | ACAAGTTTGCTGGTT[C/T]TGAGGATGGAGGAAG | 114088 |
rs185724924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011231 | ATCTCTCTGAGCAAG[C/T]GGTTTCTGCTTCTAA | 114088 |
rs185801553 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985834 | ATACGGAAAGCAGGC[C/T]ACAGACAGAGACTAG | 114088 |
rs185802126 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037857 | CCTTGGGAGGGTAAA[A/T]GCCGTTCTTGTTACA | 114088 |
rs185810773 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006981 | TGTTCACTCCAGCTC[A/C]ATCTCTACCATCCTG | 114088 |
rs185831948 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051859 | GTGATCCCAGCTACT[A/G]AGGAGGCTGAGGTGA | 114088 |
rs185874129 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980179 | ATTAAGAACTTGGAG[A/G]CTGTCTGTGAAATGA | 114088 |
rs185878969 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080835 | AAGGAGGAGGAGGAA[C/T]AGCTGCTATATCCAG | 114088 |
rs185885472 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020815 | ATCATCAAAAAATTC[C/G]TCCTCCAGATTGCTG | 114088 |
rs185894779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023227 | ATTAAGCAAAACAAA[A/G]CTTTAGTTCATAGAG | 114088 |
rs185897102 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071513 | TGATAAAAATTCTGA[A/G]CTGCAGCTGGGTATG | 114088 |
rs185907876 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049123 | CTGGCATGCAGAAGC[A/G]CAGTCCCGGCTCACT | 114088 |
rs185917426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028303 | ATTCTCTTAAGCTTT[A/G]TCCACTTGTAGAAAT | 114088 |
rs185962444 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097390 | GTAATTACAAGAAGA[A/G]GTAGGCACAATTATT | 114088 |
rs185983209 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054460 | GTATTTTTTTTGTTA[C/G]AGATGGGGTGTCATT | 114088 |
rs186018247 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002359 | CAAGATGGTCTCGAT[C/T]TACTGACCTCATGAT | 114088 |
rs186102526 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077217 | TCTACAGTGTAATGG[A/C]ATACATATTCAACTG | 114088 |
rs186113483 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072158 | AGGAGGTTCCAGGAA[C/T]AGCCTCAGTTCTTTC | 114088 |
rs186162630 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002876 | TGCCTGTTAAAACTG[C/T]AGGCAATTGGTTTAG | 114088 |
rs186196812 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091309 | TGAGTGTGTAAGATG[A/G]TGATTTATGCCTGTG | 114088 |
rs186204265 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084788 | TATATCTAGTAAAGT[C/T]AGCTGTTGATTTTTG | 114088 |
rs186224289 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042613 | TTTACCCTGATGTTA[C/T]AAAGGTAAACCCGAT | 114088 |
rs186289835 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018498 | TTTGTGTTCTTAATA[C/T]GTGATATAATTAATT | 114088 |
rs186321338 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023971 | ATAATCAACTGGTAG[A/G]CATTTAGTAATTGTT | 114088 |
rs186342879 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036901 | ATAGTTGGCTTTATT[C/G]CATCCATATTGTGTA | 114088 |
rs186352426 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975317 | TGACAATTTTTTCTA[A/G]TATAGTAGTTGTATG | 114088 |
rs186356273 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997328 | GTATAGCTAAGAAGC[A/G]AAAATTCTCTAGAGA | 114088 |
rs186368143 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065569 | AAGAAGTAAGGACAC[A/C]CATTTTTGCCCTCCT | 114088 |
rs186431493 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085509 | ACATATTCCTTTTTA[C/T]ATGGTGAAAGGTGGA | 114088 |
rs186442381 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066291 | AGACTTTTCATCCCC[A/G]TTGCTTCACTGAACC | 114088 |
rs186442767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982835 | TCTAAATGCCACCTA[C/T]AAATATCACACTCGA | 114088 |
rs186447662 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042925 | TTCTAGGAATGTAGG[C/T]ATGTAAATATATACA | 114088 |
rs186454447 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024569 | TCATTATTTTACTGT[C/G]TTATACAGTTTATGG | 114088 |
rs186520051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082794 | AAAAAGTGACTTGTT[A/G]TTCCCATATAAGAGC | 114088 |
rs186521605 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998250 | GAGGGGCGAGGGAGG[C/T]AGTGTCGCTCAGTGG | 114088 |
rs186650768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067011 | TTTAACAGGACTGAT[A/G]ACTTCTAAATTTATC | 114088 |
rs186728228 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995911 | CAAACAAAAAAGAGA[C/T]AATTATTTGATCCTA | 114088 |
rs186732237 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057726 | CAAAATCATGGCCTT[C/T]TAATCTGAATGTATT | 114088 |
rs186735432 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016674 | ATTTTGGTATCTGCA[A/G]GGAATCGTGGAATCA | 114088 |
rs186735909 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976465 | TGCCTGTCTGTTCAC[A/C]ACTGTGTCCCCACAG | 114088 |
rs186738052 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035624 | GAACGCTATACCACC[C/T]GGAAGAACATGGTGG | 114088 |
rs186739305 | snp | A/T | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086412 | AGTACATTTTAGCAA[A/T]AAGTATAAAATACAG | 114088 |
rs186768327 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060569 | CTTCCAGGGTTCACA[C/T]CATTCTCCTGCCTCA | 114088 |
rs186806885 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976797 | AGGAGAGGTAAGAGG[A/G]TAAGAACATTCTAGC | 114088 |
rs186832413 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021559 | ACCACCTTCATGTCC[C/G]TGCCTCCTCCTGCTC | 114088 |
rs186931833 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096292 | GAGAGGGAGGAAGGA[A/G]GGGGGGGGGAAAGGA | 114088 |
rs186977846 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081380 | GGAGAAATTCGATCA[C/T]TCATACACTGCTGGT | 114088 |
rs186992225 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038459 | GCTTACCACCTTTGG[C/T]GGTGGTCGGATTGCT | 114088 |
rs187001808 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008736 | TCAATTCTGGACTCC[C/G]CTGATTTATATCAAT | 114088 |
rs187014262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015474 | TTTCTTTATCTTTTT[A/T]AAATAAATGCTTTTT | 114088 |
rs187019906 | snp | C/G | 0.000123419 | 0.00785456 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983462 | GCTATGAAACAACAA[C/G]CAGGTTGATAAAAAT | 114088 |
rs187024137 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999318 | ACAGGCACTGAAAAG[G/T]CAAAGTCAGGAATGA | 114088 |
rs187043390 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050117 | TATTAAATCACCATA[A/T]GGCCATAGGACACCC | 114088 |
rs187118456 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004769 | TCTGAAGCCAAGCAG[C/T]CTGGCTCCAGAGGCT | 114088 |
rs187160303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062953 | GCTAAGCCACATGAG[A/G]TATGTGGAGAAATAG | 114088 |
rs187166611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038862 | CAGAGCAAGTGGCTA[C/T]GGTTCAGTTCAGAAG | 114088 |
rs187202431 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986340 | TCAGGACCCAAGACC[A/G]GAGGACACCTCGAAC | 114088 |
rs187216638 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029145 | ATTCTTCACGTGGCC[G/T]TTTCCCCTCAATTCA | 114088 |
rs187251916 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058870 | TTGCTGATTCTTAAA[C/T]ATAGTGAGTTATATT | 114088 |
rs187262617 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009332 | TTACTCCCAAACTGC[C/T]TTGAGGACTCATACT | 114088 |
rs187344782 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987318 | ATAACTGGAGCACGT[G/T]TGTGTGCAGAATATC | 114088 |
rs187379677 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089241 | ATCCCTGATAAAACT[C/G]ATAAACAAATGATAT | 114088 |
rs187386952 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069486 | ACAAAGAATTGCCCA[A/C/T]CCCCAAATGTCAACA | 114088 |
rs187387399 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991773 | CAGAGGTCCTCAGCT[C/G]TAAGTCCATGGTTTT | 114088 |
rs187422211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076817 | TCACAGCCTACCACC[A/G]TCCTTCCCACTGCAA | 114088 |
rs187559481 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977790 | ATTTCTTTCTGGGGT[C/T]GCATAGATGATTGCC | 114088 |
rs187568880 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000252 | ATAACTAATAATGAA[C/T]GCTTGCTATGTTCTA | 114088 |
rs187580574 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053974 | CAGTTTAATCAGCTA[C/T]CATCTCTAAAGATAG | 114088 |
rs187581020 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988121 | AGATTTTTTTATTAA[A/C]AAGAATTTGCTTGGA | 114088 |
rs187583610 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022289 | AATTATCATGGGAGT[A/G]GGCTCCCAATAAAAG | 114088 |
rs187587691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011046 | GTGGGGGACCTGGAA[A/G]GCCAAGGTGGAGCTT | 114088 |
rs187589478 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092978 | CAGGTAACTGGGGAA[C/G]AGAGCTTCAGGCTGA | 114088 |
rs187595397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029925 | TAATTGTTTAATCCA[C/T]GGTGAGAGCATGTAC | 114088 |
rs187596759 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073501 | ATGCAACAATATAAG[G/T]GGATCCAAAAAACAT | 114088 |
rs187600138 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051411 | CAGAGGACCTGTGAA[C/G]CTCTTAGCCAAAACT | 114088 |
rs187646296 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983307 | ATAAGACAAGTTGCC[G/T]CCATTTATTTTGTGA | 114088 |
rs187655812 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014156 | TCAATGATGCATTCA[G/T]GTACTGAAATAAATA | 114088 |
rs187663639 | snp | C/T | 8.23893e-05 | 0.00641778 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025336 | CCCTGTCTGACAGTC[C/T]GTTCAGCGCCTGGGA | 114088 |
rs187702127 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061641 | CTAGGAGCTTAATGA[C/T]TGTAGCTTATACTTT | 114088 |
rs187707997 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038654 | GAATGGGGTATTCAG[G/T]TCTTTTCATCCACAT | 114088 |
rs187801933 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093949 | CCCGTGCGCCGGTTA[A/T]GATTCCCCCATGCCT | 114088 |
rs187879268 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044269 | GGAAGGGTCAACAAT[C/T]CAAATTGTTGCAGGG | 114088 |
rs187899251 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088327 | CATTGAATCAAGTGG[C/T]TTTGTTTGTTGCAGG | 114088 |
rs187913203 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044882 | TTCTGTCGGCAGTCA[C/T]TTTTGTTTTGTTTTT | 114088 |
rs187935570 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004437 | CATTTTATTTGTTTA[A/T]TTTTTTTTTTCAGTG | 114088 |
rs187947087 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079010 | TTGTAAACCTCAAAT[A/G]TGCACAATACAATTT | 114088 |
rs188003418 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031111 | TGTGATTGCGCCATT[C/G]CACTCCAGCCTGGGC | 114088 |
rs188020592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005100 | AAAGCTATTACCGGT[A/G]CACTGTTAAAGATAA | 114088 |
rs188031839 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026720 | ATGCACACCAAATGC[C/T]TGGTTGAGGCAATGT | 114088 |
rs188043767 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045596 | TAGCATAAATCCACA[C/T]TGGTAAAGAGTAAAT | 114088 |
rs188090691 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993646 | GTAAAGTCCTCCTTC[C/T]GGCTGGGATTTCTGG | 114088 |
rs188092406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029314 | GCACTGGCAGCTTGA[C/T]GGCTCAGAAAATGAC | 114088 |
rs188096652 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000490 | CATAAGAAGGGTAGG[A/G]CAGTTTCAGAGACTG | 114088 |
rs188099409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083807 | AACAAAAAATGTGAA[C/T]TTCTGACATTTTGAA | 114088 |
rs188107421 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064487 | AAAAAGTGTATTTTA[A/C]ATATAAAGAATCAAA | 114088 |
rs188188315 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069043 | AGATTATTTCAATAG[C/T]GTAGGTGAAAGGACA | 114088 |
rs188223061 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025936 | GCCCTAGCACATTTG[A/T]GTCCTCTCCTCACTA | 114088 |
rs188312858 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997822 | TTATCAAAGGAAGCC[A/G]CCGGCCCAAGCCATT | 114088 |
rs188320815 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019322 | AGCTTTCTGACATTC[A/G]CATTAGTTCACCACA | 114088 |
rs188337280 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089647 | AGAGAAAAACAGAAT[A/T]CTTTTGTTTAATATA | 114088 |
rs188341465 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037498 | AACTCACAATGGTGA[A/T]CAGATCAGAAAAGAA | 114088 |
rs188368716 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978311 | TTGTGGAATGAGGCT[C/T]ATAGTTGTTAATGAG | 114088 |
rs188390764 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022471 | ATTATTTATAATCAC[C/G]CAGTCTGTGGGATTC | 114088 |
rs188421745 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092219 | CAAAAATTTAAATTC[A/G]ACTGTTCTGAAAACA | 114088 |
rs188423237 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080225 | TATCGAAAGCCAATG[C/T]TAAAAAAAAAAAGAA | 114088 |
rs188431177 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059027 | CAAGTTAGAGAACAG[G/T]CCTGTAAAGGAAGAG | 114088 |
rs188443541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050574 | TTTAACAATGTGACC[C/T]TCCAACAGCAGAGGG | 114088 |
rs188456663 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058166 | CCTAAGCCAGCACTA[C/G]TCAGTCTCCCAGAGT | 114088 |
rs188464588 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036039 | CCAGCACTCTAGGTA[A/G]AAGCCACAGAGACTT | 114088 |
rs188530963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985544 | CAGGCTGGATGCACT[A/G]ATCCAGTCTCCCAGA | 114088 |
rs188535017 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006607 | AGCATATAAATTAAC[C/T]AGGCAGAGTGATAAT | 114088 |
rs188543472 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079818 | AGACTGTACACAGGT[C/T]AGAACAAGCCATAGA | 114088 |
rs188545338 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027269 | CTGCCTCAGCCTCCC[C/G]AATAGCTGGGATTAC | 114088 |
rs188675120 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990061 | TCACTTGGTCATCCA[A/G]GCTAGAGTGTAGTGG | 114088 |
rs188686126 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012717 | ACATCCTCGCCCACA[C/G]TTATTATTTTCTGAT | 114088 |
rs188695531 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052433 | CTGGGAATTAAATTT[A/G]ATTATCAACAACCCC | 114088 |
rs188705668 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081903 | CCACGTGTTCTCTAA[C/T]CTGGAAACTTTCCAA | 114088 |
rs188738603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011358 | AATCTTGAATGCCTA[C/T]ATATTTTTTTATTTC | 114088 |
rs188883786 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995282 | TGTTTTTCAGTGTTT[A/C]TCACAATGTGTAAAA | 114088 |
rs188933985 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078456 | ACACCAACAGACAAA[C/T]AGATAAAGAAAATAT | 114088 |
rs188950995 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035353 | TGGAAACTTGAGGGA[G/T]GAATAAGAAGTCTAT | 114088 |
rs188960402 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014014 | CAAATGACATCTGCC[C/G]TTGACTACAGGTACT | 114088 |
rs188965808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074771 | TTCTCCTCTCTCCAC[C/T]TAGCTGTCATTCCAC | 114088 |
rs188969019 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032601 | GGTTAGCTTCAGCCT[C/T]AGTTCAATCCTGGCT | 114088 |
rs188988520 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075914 | AAAGGTGATTACACA[A/G]GAATTCAACAAATGT | 114088 |
rs188996713 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053860 | TACAAATTATTGCCC[A/T]AAGTAAAGACTAACT | 114088 |
rs189001816 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075165 | GAGGAGTTAAGTGGG[G/T]CGCCCAAGGAGGTAG | 114088 |
rs189011138 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988862 | TACCTTAGATTTCAG[A/G]AGTCTTAGAGGGAAG | 114088 |
rs189026280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030709 | TGTATGTATGTGATT[G/T]TATGTGAGATATGTC | 114088 |
rs189030225 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002364 | TGGTCTCGATCTACT[A/G]ACCTCATGATCCACC | 114088 |
rs189074705 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095812 | TTTCCTAGTGTCGAC[A/G]TGAGATTCAACTGGG | 114088 |
rs189161784 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978988 | GATTTTCTGATAATG[A/T]TACTAATGCTTCAGT | 114088 |
rs189172103 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016244 | CCTCAACCCCCGGGC[C/G]GTGGACTGGCACTGG | 114088 |
rs189178011 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984595 | TCATATTCAGCTTGG[A/T]AATAAGTTTGTAGAA | 114088 |
rs189192425 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026787 | GATTCTCGCTCTATC[C/T]CCTATAAGTGTGACC | 114088 |
rs189223053 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056474 | CAGATATGCTATACT[C/T]TAGATCCCAGAGCTC | 114088 |
rs189236158 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070325 | ACAGAAACATACATA[A/T]AACAAGTTTATGCAT | 114088 |
rs189277840 | snp | A/G | 4.94434e-05 | 0.00497184 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094199 | GCACTGGTAGCACAC[A/G]GGCATCTTGCATTGC | 114088 |
rs189297954 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053433 | TCAGTACTCAGTTTG[C/T]ATCAGTTTGTAGTTC | 114088 |
rs189324168 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023388 | GAAGAAAAAGGATGG[A/C]ACTGGTCTTCAATAT | 114088 |
rs189372722 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040753 | TGTGAACCTTTCATA[C/T]TAATGATGAACCACA | 114088 |
rs189438943 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979951 | CTTTGGGCTATCAGA[C/G]CTCTGACTCTAGGAA | 114088 |
rs189443999 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002276 | ACAGGCCCCTGCCAC[A/C]ACGGCTGGCTGATTT | 114088 |
rs189450517 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083432 | GCTAATTAAAAAAAA[A/T]TTTTTTTTTAGAGAT | 114088 |
rs189454489 | snp | A/G | 0.000131778 | 0.00811614 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022901 | TCTTCTGTTGAGGGC[A/G]TCGATGAGGGCATCA | 114088 |
rs189462365 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063944 | TATATGTGTGTGTGT[A/G]TATAATATATAACAG | 114088 |
rs189468253 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006049 | GGCAACAACAATGGC[A/G]TCTATGATGAGCTTT | 114088 |
rs189528143 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048337 | TACAGACCCTGTGGA[C/T]AGGAGCCACATTCAT | 114088 |
rs189541388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090655 | AGGCTACAGTGCAGT[A/G]GTGAGATCCTGGCTC | 114088 |
rs189546157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017580 | ATTGGGCAGTCCCAA[A/C]CACACAGGAGAACAT | 114088 |
rs189565243 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048862 | GGTGATGGACGTCTG[C/T]AGTCCCAGCTACTCG | 114088 |
rs189588576 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983659 | AATTGATCCTAAACT[C/G]TGTAGCTGAATTTTT | 114088 |
rs189596805 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974977 | CTGCACTCCAGCCTG[A/G]TGACAGAGTGAGATT | 114088 |
rs189651336 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054805 | CGGCCTCCCAAAGTG[C/T]TGCGATTACAGGCGT | 114088 |
rs189659481 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033613 | CTACTCCCTTGTCAT[C/T]CTTGGCCATACGGCT | 114088 |
rs189723907 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993163 | GGGCAAATCTCGTCA[C/T]TGCCAGCCAAGAGTA | 114088 |
rs189731538 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015241 | GAGCAACTCAGGAGA[C/G]AGTACACAATACACA | 114088 |
rs189813804 | snp | A/T | 0.0197687 | 0.0974348 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996364 | AGACACCATAATCTT[A/T]TGAACATTAAAATAA | 114088 |
rs189814491 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080106 | GCTATGTGTTTTCTG[C/T]GTGAGAGGCATAGCA | 114088 |
rs189825625 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071131 | CATCTGTAATCCTAG[C/T]ACTTTGAGGCCAGGG | 114088 |
rs189827143 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036608 | GTAAATAATTGTTAC[A/G]CTATACTATTTATGG | 114088 |
rs189860592 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975343 | GTATGCATCTGTAAT[C/T]GCAATTCAGTGTAAA | 114088 |
rs189989864 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980632 | TTCACTCCTGCACTT[C/G]AAAACAAAGACGCTA | 114088 |
rs189995151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022693 | GGAGGTGTCTGTTCC[C/T]TTCTGGCCAGACCAC | 114088 |
rs190001379 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991583 | CCTTATATGATCCTT[C/T]ATCAATCATTTTCTA | 114088 |
rs190064264 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063701 | ATTTTTAAAATACTA[A/C]AACAAAAATAAAACT | 114088 |
rs190069617 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058419 | TAGGTCATTGATTCA[A/G]GTACTTGTGAATTGT | 114088 |
rs190097405 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018139 | TAATGGAATAACTGA[A/G]TTCTTTGTCATTAAT | 114088 |
rs190166264 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987804 | TTTATTTATTTAGTA[C/T]TATTTATTATTTTTT | 114088 |
rs190178322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009692 | TTCTCACATTTTAAG[C/T]ACATCATCTTCATGT | 114088 |
rs190184735 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029344 | CCCAGCTGCCTCCCC[A/G]GGCGTGGGGCACCTT | 114088 |
rs190197115 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051211 | ACTATAGGAAACCTT[C/T]GTTGTTCCTGAAAAT | 114088 |
rs190202897 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081045 | CGCAGGTCTGTGTCT[G/T]CTTTTTTCCTCCTGT | 114088 |
rs190213070 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060147 | TTTCCACAGACTGTA[G/T]TTGGCTTCTAGGATA | 114088 |
rs190310223 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071646 | TGTCTCTACTAAAAA[C/T]AAAAAAAAAATTAAC | 114088 |
rs190316220 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049509 | TCCTTCATTCAACAA[A/T]TATAGTGTATGTGTA | 114088 |
rs190321162 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040223 | TTAAATAGATATCCA[C/T]AAAATCCTCAAGCCA | 114088 |
rs190336776 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001767 | CGTTTCAAAACTTCC[A/G]AGGAACCTGATGTCA | 114088 |
rs190353038 | snp | A/C | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096846 | GCACTTGCAGGATAC[A/C]CTTAATTTATAGGTC | 114088 |
rs190365214 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054094 | GAAATCATTTTGACA[C/T]CATTAAAAAGTTAAA | 114088 |
rs190372368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007223 | GACATATTTTTTCCT[G/T]TAAGCTACTTGTGAC | 114088 |
rs190380214 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028815 | AGCATGCTGAGAATC[A/C]CCGAGGTCTCCCAGA | 114088 |
rs190382159 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977003 | TAAAAAATTAAGTTA[A/G]ATAAAAGCAAAATCT | 114088 |
rs190386643 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000102 | AAAGGTTGCTTAGAA[C/T]AGGGAAGCTATAACA | 114088 |
rs190397077 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090998 | GTAGTGGTTTCTATT[G/T]CCCATTTTAAAGTAT | 114088 |
rs190526467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982765 | GAGCAGTAGGAATTT[C/T]GGACATTAGGTGCAG | 114088 |
rs190530928 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996489 | CCCATGATGTATTAT[A/G]AATAGAAATAGTTTT | 114088 |
rs190540579 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003066 | GGAAAGAGAAGGACA[C/T]AGAAGACATAATGCC | 114088 |
rs190605748 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076927 | ACCCTATACTGCCCA[A/G]TGCCATTTGGGCAGT | 114088 |
rs190647617 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087024 | CAGCTGGGGTGGGGG[A/G]AGGTGGCGGGCACTG | 114088 |
rs190675736 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077539 | GCTGGGACTACAGGC[A/C]CACACCACCATGCCT | 114088 |
rs190746068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078073 | TATCAGATGAGCCAG[C/T]GGTCTCATCATCAGT | 114088 |
rs190756525 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055834 | ATACAATGTACATTT[C/T]AGAACCCATGAATAC | 114088 |
rs190764636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035033 | GGAAAATATTTATAA[C/G]ACATTAAGTGAAAAG | 114088 |
rs190805155 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983022 | GAAGCAAAATTGACA[C/T]GGATAAGAAAATGTG | 114088 |
rs190809157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003659 | GATAAAAAAAAAAGG[C/T]TAGACTCTCAATAAT | 114088 |
rs190819384 | snp | A/G | 0.000181589 | 0.00952687 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025230 | AGTTACGTATTAACC[A/G]GCGGGTTTCCTTGCG | 114088 |
rs190824166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986762 | AGGGAAAGAGCCTTA[C/T]CTTTGTTTCTGAATT | 114088 |
rs190842584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025886 | CACTCCTGCCTCATC[C/T]GTGTCCTCTTCCTTC | 114088 |
rs190847709 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066857 | AAGCTCTGCTGTTGT[C/G]ATTGGCTGAGACTTA | 114088 |
rs190856319 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043031 | ATAACTTGCTTATAA[A/G]AGGTCCTAAAATGTA | 114088 |
rs190901204 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072271 | TCTTATTATTTTACT[A/G]CATTAAAAAAAACAC | 114088 |
rs190913363 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067551 | ATCTCTCTGACCTTA[G/T]CTCTTACCATGTCTC | 114088 |
rs190923397 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097490 | GCTGGGATTGGAACC[C/T]GGACACATATAAGTT | 114088 |
rs190933094 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086098 | AGTAATTTTCATATA[C/T]GAGAACTAAAGGAGT | 114088 |
rs190939447 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029239 | CTGAAGTTACAGGCA[A/C]AGGATGGGTCAAAAG | 114088 |
rs191076558 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008967 | TTTTCATTACATAAG[C/T]TAGAAGCCACTCCAT | 114088 |
rs191093965 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021089 | CAGTTCTATGTGATT[C/T]GAATGATATTTTGAG | 114088 |
rs191100965 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995987 | AATAAGCTATTCACT[A/G]TATTTTTTCTTGCTT | 114088 |
rs191107013 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017009 | AAAGCATGATGACCA[A/G]CTGATGCTTTGAATT | 114088 |
rs191136580 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079056 | AAAATAAAATGCTCT[C/T]GATTAATTTTTGATG | 114088 |
rs191142753 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057840 | AACATTCATATAAGA[A/G]ACAGGAGGTAAGTGG | 114088 |
rs191144218 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091467 | TTAGTATAGTTCTTT[A/G]CTGTCCTATTTTTGC | 114088 |
rs191152822 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035643 | AGAACATGGTGGCCC[A/G]GTGTGGACGTGAAGG | 114088 |
rs191157982 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050228 | CTGTGTCCCCACCCA[A/G]ATCTCATCTTGGATT | 114088 |
rs191180669 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976562 | CTTTTATTAAATAAA[C/T]GAACCAAATCATTAA | 114088 |
rs191216249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092402 | TGAAAATTAATGACA[C/T]TTTTTTCTTGCTGTA | 114088 |
rs191328042 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998697 | AACTGTCACAGAGAT[C/T]ACACTCCAAGCCACC | 114088 |
rs191387042 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061955 | GATATTATCCCACAC[A/G]TTTCAGACCATCTAT | 114088 |
rs191397358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038714 | ATGAACTAGGAATTC[C/T]GTGAGACTGAGCTGG | 114088 |
rs191398760 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038097 | GATGTGATTAAAGTT[A/G]TAGACCTTGAGATGG | 114088 |
rs191439957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977848 | ATTTTACCAATTTCC[A/G]TGTATCCCCAAACCT | 114088 |
rs191442442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000434 | TGGAGGAGACCAACT[C/T]GAATGCAGGCAGTCT | 114088 |
rs191454414 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022299 | GGAGTGGGCTCCCAA[A/T]AAAAGGTTGAAGTTT | 114088 |
rs191457987 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081730 | GATAATTCACTAGAA[G/T]GACTCACAGAACTCA | 114088 |
rs191467521 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072855 | AGAGAGCAATGTACC[A/G]TGTAGGAGATGATTT | 114088 |
rs191474622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081921 | GGAAACTTTCCAAAT[C/T]TTGTTGTTCAAGAGT | 114088 |
rs191478979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038478 | GGTCGGATTGCTTCA[C/G]CTGATATTTTGTAAA | 114088 |
rs191628620 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024022 | ATAAGGAATGCATTA[A/G]TAATTGCTTGAGCAA | 114088 |
rs191685073 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075280 | GAGCCCCACTCCCAC[A/G]CCTACTCCACGTTAA | 114088 |
rs191691017 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985876 | CACCACGCACATGAA[A/T]GGCAAGAACAAGACA | 114088 |
rs191703914 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082967 | AACTGTGACTTTGGG[A/T]TTCTTGGTTTCTTAG | 114088 |
rs191724926 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060623 | AGGCGCCTGCCACCA[A/C]GCCCGGCTAATTTTT | 114088 |
rs191725205 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065673 | AAAGTGGCCATAGAG[C/G]CCTGGAGTTGGGATT | 114088 |
rs191730694 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021593 | TGCCAGCACTATGAG[C/T]GTAAGACCAGACCTC | 114088 |
rs191744027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994683 | ACATAGCATAAACCT[C/T]AGAACTCTGTGTATT | 114088 |
rs191884074 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014459 | CTTTTTTACATTTTA[A/G]TCAACCATTCACAAT | 114088 |
rs191966555 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979201 | AAGTATAAAGAAGGT[G/T]CTTATGCTTGGCGTG | 114088 |
rs191973190 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030480 | AAGCCCAGCAAAGGG[C/T]TGGCGCAGTGAACAG | 114088 |
rs191977962 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001923 | ATGTCTTTGCAGCCA[C/T]GTGAGAGTCTGTCAT | 114088 |
rs191988666 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022735 | GGCTGTGGGCATCCT[C/T]TCCTCCTGTCCATGG | 114088 |
rs192006033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093377 | GGTTTCCCTAGGAGA[C/T]GCACCTGTCTGGCTT | 114088 |
rs192012053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084888 | GCTTTGGATGAGCTG[A/G]GCTTACAGTTGAGCC | 114088 |
rs192019221 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074205 | AGGAGGATCACTTGA[G/T]CCCAGGAGTTCAAGA | 114088 |
rs192027539 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042735 | GGCTTAGTCTTATTT[G/T]CAGGTAGGGGTGGAG | 114088 |
rs192028512 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051738 | TTGGGAGGCTGAGGC[A/G/T]GGTAGATCACTTGAG | 114088 |
rs192046379 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016114 | AAATGGCATGGTACT[A/G]GCATATTACCTATGC | 114088 |
rs192221975 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004496 | ATCCAGAATTCCTCT[G/T]TGAAAGTACACAGGA | 114088 |
rs192271752 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079936 | AGAGGGAGAATGAAG[A/G]AGTAGAGAGTGCTAG | 114088 |
rs192278634 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058358 | CCTTGCCTACTCTAA[C/T]GACATTCTTGGTTGG | 114088 |
rs192279887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033393 | ACTGTGCCTAGCCCA[A/G]TGATGTTTTTATAGT | 114088 |
rs192281829 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991791 | AGTCCATGGTTTTAG[A/T]GATGAGAAAACTGAA | 114088 |
rs192319387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983505 | CTTAAAAAGCACCAG[C/T]TGAATATAGATACCA | 114088 |
rs192326477 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004896 | TTCTGTTTCCTATAA[C/T]GTGAACAATAAAGAT | 114088 |
rs192336359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026466 | ACTTGATACAAATTC[C/T]TTCCCCTCCTAGCAG | 114088 |
rs192502671 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989590 | GAGCTCCTGAAGAGA[C/T]GTTTAACATCACATC | 114088 |
rs192509817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075029 | CAAAGAGACTCTTGT[C/T]AGGAACTGAGTCAGA | 114088 |
rs192522253 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031010 | AAAGTTAGCCAGGCA[C/T]GGTGGCGGGCGCCTG | 114088 |
rs192528362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089483 | GTCTCTTACTTTATG[C/T]AAACTGTGATTTGAC | 114088 |
rs192531816 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070005 | CAATGTGTAACTTCA[C/T]AGCTGAGGTTGATCA | 114088 |
rs192540653 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046782 | ATACCTTCGTTTCCT[G/T]CTTAGTAAAGTGGAA | 114088 |
rs192564469 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005215 | CGCTAACCCTCTGGC[A/C]GCTTTCCCCCTATGA | 114088 |
rs192570369 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026725 | CACCAAATGCTTGGT[G/T]GAGGCAATGTGGGAT | 114088 |
rs192623460 | snp | A/C | 0.000735474 | 0.0191624 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983440 | TAAAGAGATACTACA[A/C]ATCAACGCTATGAAA | 114088 |
rs192653737 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978559 | TAAGGCTCAGCTCAC[A/C/T]GGTAACTGCGATAAG | 114088 |
rs192727185 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063342 | CAGAGATTCAGTGGC[C/T]TGCAAGAAATAACTA | 114088 |
rs192733233 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022488 | AGTCTGTGGGATTCC[A/G]CTATATCAACATAAA | 114088 |
rs192754637 | snp | A/G | 0.00914312 | 0.0669923 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095567 | CGAGTGCTGCGCAGC[A/G]CGGAGGACGCCCCTT | 114088 |
rs192804366 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094032 | CCCCACTGGGATGCG[C/T]TGTGCGCAAGAGACG | 114088 |
rs192809691 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011102 | GCTGAAGAAAGAAGA[C/T]GGATGCAGAATTAAG | 114088 |
rs192810179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011796 | ACTTTGACATTTCTT[C/T]TTAGTTTTTCTCTGG | 114088 |
rs192811299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052583 | GCACAGTCTGTCTGA[C/T]ATTTCATCTTTTCAA | 114088 |
rs192832214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040399 | TCTGTTGCCTGTACC[C/T]GGCAGCACCCGACAT | 114088 |
rs192874897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083366 | AAGTGACTCTCCTGC[C/T]TCAGGAGGATCCTCA | 114088 |
rs192886433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001652 | TATTCCATCATTTTT[C/T]TTTAAAACCAGTGAT | 114088 |
rs192931298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039048 | AAATGCCTGGGAAAT[A/G]TTAATCACAAGATCT | 114088 |
rs192997216 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036186 | GTTGATGAGCCAGCC[A/C]ACGGCACAAAAAAGC | 114088 |
rs192999443 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069345 | AGAGGACATTGGCAA[C/T]GTCTACAGGCAATTT | 114088 |
rs193012956 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988259 | TTGAATTCCCAAGCA[C/G]TTATCTGAAAACCAG | 114088 |
rs193072846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016311 | GGTGAGCGGCGGCCA[C/T]CTCCTTTCAGATCAG | 114088 |
rs193074816 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983877 | ATTAAATATAACTAA[A/G]TGTGTAATGTAATCC | 114088 |
rs193082768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063873 | CGGATTGAAACAAGA[C/T]TGCAACTTGAAACCA | 114088 |
rs193109581 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056524 | CTGACATTCAACAAA[C/T]AAGTCCAACATTTTC | 114088 |
rs193179621 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017608 | CATTTACCACTGAAG[G/T]TGGGTTGCAATAAGA | 114088 |
rs193180979 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045338 | GTGAGGGTGACACTC[A/C]GACACATAAAACAAT | 114088 |
rs193202052 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088733 | CAAAAGGCTAATAAA[A/T]GCTACCTAGTGGTGA | 114088 |
rs193236830 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995680 | TTGTTTTGAAGTTTG[A/G]AAAGGGATTAACTCT | 114088 |
rs193261752 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078555 | TGCCACTTGCCACAA[C/T]GTGGGTTATGCTAAG | 114088 |
rs193265712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035416 | AGAGTGCAGTCAAAT[A/C]ATTTTTATATGAAAA | 114088 |
rs199555272 | snp | A/G | 0.000698983 | 0.0186816 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094074 | CTGCAAAACCGGATG[A/G]TCGGAGACGCAGGGA | 114088 |
rs199613048 | snp | A/G | 0.0039919 | 0.0444974 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983389 | ACTTGCCTAATTGAG[A/G]GTAAGGTGCAGATTG | 114088 |
rs199645165 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979376 | TTTAACCTCAGGGGC[A/G]GGGTGCTTACCTGCA | 114088 |
rs199666878 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010141 | AAGCGAAAAAAAAAA[A/G]AAAAAGAAAAAGAAA | 114088 |
rs199671884 | snp | A/G | 0.000297201 | 0.0121866 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025221 | CCGCCACACAGTTAC[A/G]TATTAACCGGCGGGT | 114088 |
rs199673072 | snp | A/G | 0.000122212 | 0.00781608 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983420 | TGTCTCAAAATTGCA[A/G]CCTATAAAGAGATAC | 114088 |
rs199777158 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992414 | AGACCCTGTCTCTAC[-/G]GGAAAAAAAAAAAAG | 114088 |
rs199780285 | snp | A/G | 3.06133e-05 | 0.00391225 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997984 | GGTGGGGTTACCTCC[A/G]GGCTTGCCAGCCACT | 114088 |
rs199809498 | in-del | -/AT | 0.0138799 | 0.0821421 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995910 | ACAAACAAAAAAGAG[-/AT]AATTATTTGATCCTA | 114088 |
rs199897555 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060291 | CAGCCTAACTTCCTA[C/T]GACCATTTAGCTAAC | 114088 |
rs199920531 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070517 | TGGAAGTGTTTCAGA[-/T]TTTTTTTTTTTTTTG | 114088 |
rs199949161 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053557 | TACATTTATTTATTT[A/T]TTTTTTTTTACTTTT | 114088 |
rs199999838 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072993 | TTAATGTTTTATTTA[-/T]TTTTTTTTTGGCAAC | 114088 |
rs200001803 | snp | C/T | 0.000131904 | 0.00812002 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000740 | TCCATCGGCGGGCAC[C/T]GTGGACAGAGGTGGC | 114088 |
rs200018750 | snp | C/T | 0.000231627 | 0.0107592 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982072 | GATGATGTCCGAGTG[C/T]GCCGAGCCAGGGTCG | 114088 |
rs200045628 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083424 | CATGCCCAGCTAATT[-/A]AAAAAAATTTTTTTT | 114088 |
rs200084466 | in-del | -/ATT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062102 | AAGTCCAATAAATAA[-/ATT]ATTTATTTATGATAT | 114088 |
rs200085628 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995960 | CAGATCGATCATATC[-/T]TTTTTTTTTAAAATA | 114088 |
rs200114910 | in-del | -/C | 0.00438332 | 0.0466095 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976855 | CATTCTTCCCTACCT[-/C]CCCCCTACAACCTCA | 114088 |
rs200192609 | snp | C/G/T | 0.000115334 | 0.0075931 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000770 | CTGTTTCCAGGACAA[C/G/T]GTAGCGCTGTTGTTG | 114088 |
rs200195393 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979545 | TTGTGATCCCTCCCT[C/T]AGTTCTGTAGGAAAA | 114088 |
rs200221592 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981938 | GCAGGATCAGGGTGG[C/T]TGTCATAGCGATCTA | 114088 |
rs200246373 | in-del | -/G | 0.0162398 | 0.0886349 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003301 | TGAATGATTCCCCCC[-/G]GGGGGTATTTATTCT | 114088 |
rs200246485 | in-del | -/T | 0.215446 | 0.2476 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083430 | AGCTAATTAAAAAAA[-/T]ATTTTTTTTTTAGAG | 114088 |
rs200250163 | snp | A/G | 3.35059e-05 | 0.0040929 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997975 | GTGGGCAGTGGTGGG[A/G]TTACCTCCGGGCTTG | 114088 |
rs200287648 | snp | A/C | 6.58913e-05 | 0.00573945 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022856 | CTTGTGCTCATGCTC[A/C]TTGTTGACGCGGGCC | 114088 |
rs200305076 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004188 | TCCTTAAGAATGAAT[C/T]TCCCCTGACCTGATC | 114088 |
rs200455787 | in-del | -/CCG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085517 | TTTTTATATGGTGAA[-/CCG]AGGTGGATCAGCTTT | 114088 |
rs200497729 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071387 | GTCTAAAAAAAAAAA[A/G]AAAAAAAAAAAAAAA | 114088 |
rs200498491 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059811 | TCAAAAAAAAAAAAA[A/C]AAAAAAAACACAAAA | 114088 |
rs200506401 | snp | C/T | 3.29902e-05 | 0.00406128 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000697 | CCCGGAATTGACCAC[C/T]GTTGCCATCATCCAG | 114088 |
rs200650560 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004436 | ACATTTTATTTGTTT[-/A]ATTTTTTTTTTCAGT | 114088 |
rs200688071 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003876 | AAAAGGTGAATGTGC[G/T]AAAATTACAGCCTCA | 114088 |
rs200713374 | snp | C/T | 0.000150673 | 0.00867836 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977387 | AGTCCTGAGAGGCAT[C/T]GTGCATCCCCCTGTC | 114088 |
rs200729966 | snp | A/G | 0.000923087 | 0.0214637 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025366 | AGAGCTGGCTCTGCA[A/G]AGACAAAGAAGGAAG | 114088 |
rs200741814 | snp | A/G | 0.000115646 | 0.00760327 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022795 | CCCCTCGGGAGCCTG[A/G]CTTGTTGGCTTTCTG | 114088 |
rs200748846 | snp | A/G | 0.000467298 | 0.0152784 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009046 | GCATCCACTCAGGAT[A/G]TTGCTCTCTGACTTG | 114088 |
rs200849577 | snp | C/T | 3.30595e-05 | 0.00406554 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982066 | GGAGAGGATGATGTC[C/T]GAGTGCGCCGAGCCA | 114088 |
rs200901177 | in-del | -/T/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070516 | TTTTTTTTTTTTTTT[-/T/TT]GGATTTTGGAATATT | 114088 |
rs200923459 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053508 | GATCAGAACAGGTAT[C/T]CTTTTTTTTTTTTTT | 114088 |
rs200932195 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049179 | GATTCTCCTGCCTCA[-/A]GCCTCCTGAGTAGCT | 114088 |
rs200935253 | in-del | -/A | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096302 | AAGGAAGGGGGGGGG[-/A]AAGGAAAGGCGGAAG | 114088 |
rs200937173 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084182 | CCACACTTTTTTTTT[-/T]ATATATATTTAGTGA | 114088 |
rs200954244 | snp | A/C/T | 3.39249e-05 | 0.00411844 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094447 | GCTGGCACTTGAGGG[A/C/T]CGCGGCTTTGCTCTG | 114088 |
rs200957319 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054314 | TGTTGTTGTTGTTGT[C/T]CAGGCTGAAGTATAG | 114088 |
rs201008231 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079511 | TTTCAAAAGAAAAGA[A/T]ATTATGTGAGTGCAT | 114088 |
rs201106472 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025759 | GGGCTATTGGTCTGG[A/C]TAGGGCAGAAAGAAT | 114088 |
rs201108028 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027848 | ATATCTTTTTTTTTT[A/G]CTGAATGAGTAAAAG | 114088 |
rs201128574 | snp | A/G | 1.74662e-05 | 0.00295513 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977324 | GCTGGAGTAGAAGTC[A/G]GGGACTGGGAGCCCG | 114088 |
rs201195016 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067868 | TCTACTGTTTATTTT[C/T]TTTTGTGTTATGGCT | 114088 |
rs201201421 | snp | C/T | 0.00145664 | 0.0269481 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982114 | GGCCACTGGGAACAA[C/T]AGAAGGGAATCAGGT | 114088 |
rs201254616 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999457 | AAATTAGATTTTATC[-/A]TGCCAATAAATCAAC | 114088 |
rs201255051 | snp | C/T | 0.00011533 | 0.00759287 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025292 | GACCATGTTGCGCAG[C/T]TGTACCAGAAACTCC | 114088 |
rs201312545 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975984 | CAGCAGAGTGGATGG[C/T]TTTTTCATTCATAAC | 114088 |
rs201359496 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024376 | ATGGGCATGTGTGCC[-/A]AAAAAAAAAGGCAAA | 114088 |
rs201362082 | snp | C/T | 1.67936e-05 | 0.00289767 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094310 | ACCCTGGGCCGGGGG[C/T]ACCAGGCGGTGCTTG | 114088 |
rs201440423 | snp | G/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978758 | GCAAGATTTTTATCT[G/T]TTTTTTTGTTTTTTT | 114088 |
rs201448581 | snp | A/G | 0.00399192 | 0.0444975 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983388 | TACTTGCCTAATTGA[A/G]AGTAAGGTGCAGATT | 114088 |
rs201485579 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036304 | AAGAATTTGTTTTTG[-/T]TTTTTTTTGAGAGCC | 114088 |
rs201570933 | snp | C/T | 0.00153936 | 0.0277004 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997992 | TACCTCCGGGCTTGC[C/T]AGCCACTTTAGATGC | 114088 |
rs201591265 | in-del | -/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996360 | ATTAGACACCATAAT[-/C]CTTATGAACATTAAA | 114088 |
rs201628563 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979140 | ATCATTAGCCAACCA[C/T]GAAGAGAATTCTAGT | 114088 |
rs201632600 | in-del | -/A | 0.17461 | 0.238362 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080227 | TCGAAAGCCAATGTT[-/A]AAAAAAAAAAGAATA | 114088 |
rs201669235 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989939 | AACAAAGCAAAGATT[G/T]GCTGGGGACCACTTG | 114088 |
rs201698609 | in-del | -/TGTG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002106 | TGGGAACCATGGTTT[-/TGTG]TGTGTGTGTGTGTGT | 114088 |
rs201704742 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013226 | TTTTTTTTTTTTTTT[-/T]GCATGTGGATATCCA | 114088 |
rs201741709 | in-del | -/T | 0.0166325 | 0.0896639 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035563 | TGGATCTCAAAACTG[-/T]TTTTGCTTATCTTAA | 114088 |
rs201743944 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981962 | CGATCTACCGTGAGC[G/T]CCCAGTAGTGGATGC | 114088 |
rs201751658 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003658 | GGATAAAAAAAAAAG[C/T]CTAGACTCTCAATAA | 114088 |
rs201779029 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993736 | CTTGCAGACAGACTT[C/T]GGATAGTTTTCCCTC | 114088 |
rs201780737 | snp | C/T | 0.000314452 | 0.012535 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022785 | GTCCATCATGCCCCT[C/T]GGGAGCCTGGCTTGT | 114088 |
rs201835548 | in-del | -/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978777 | TTTGTTTTTTTTTTT[-/T]CACTGATGTATCCCA | 114088 |
rs201840743 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071646 | GTCTCTACTAAAAAT[-/A]AAAAAAAAAATTAAC | 114088 |
rs201843050 | snp | C/T | 1.66145e-05 | 0.00288218 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094283 | GCGTGGGCTCAGCCT[C/T]CGGCTCACACGACCC | 114088 |
rs201853468 | snp | C/T | 0.000577639 | 0.0169849 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025224 | CCACACAGTTACGTA[C/T]TAACCGGCGGGTTTC | 114088 |
rs201864896 | snp | A/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978768 | TCAGTGAAAAAAAAA[A/C]ACAAAAAAACAGATA | 114088 |
rs201874678 | snp | C/G | 1.64969e-05 | 0.00287196 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094153 | CCCCCAGAGCCTTGA[C/G]TTCGTGGCTGGAGTG | 114088 |
rs201922353 | snp | A/T | 0.000132946 | 0.008152 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009066 | TCTCTGACTTGGGGG[A/T]TGCAAGGACATACCT | 114088 |
rs201955588 | in-del | -/T | 0.0158469 | 0.0875917 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049836 | TCTCAAAAAAAAAAA[-/T]AAAATAAAATAAAAA | 114088 |
rs201960248 | snp | A/C/G | 0.00140093 | 0.0264295 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022992 | TCTCAACTGCAAGCT[A/C/G]CTGGGTGCCTCAGGC | 114088 |
rs201980160 | in-del | -/TTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053510 | TCAGAACAGGTATTC[-/TTTT]TTTTTTTTTTTTTTT | 114088 |
rs201992280 | in-del | -/AA | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075015 | CGGACATTTTTATCC[-/AA]AGAGACTCTTGTCAG | 114088 |
rs202003646 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023523 | TGTGTAACAGGGATC[A/C]CCCTGCCATAAAAAT | 114088 |
rs202072704 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003719 | GACAAATTAGCAAAT[G/T]GACAAAAAGTCAAAG | 114088 |
rs202077847 | in-del | -/T | 0.0111196 | 0.0737302 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980367 | GATTTGTCTTTCCCA[-/T]TTTTTTTGAGATCTA | 114088 |
rs202113109 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982590 | GCTTTGAAGTCTTCC[-/T]CGGCTCTAGTGAAAG | 114088 |
rs202140681 | snp | C/T | 0.000728155 | 0.0190669 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094687 | TAGTGGGGGCGCTGG[C/T]GAACCCCCCGTAGGA | 114088 |
rs202200082 | snp | A/C | 5.06393e-05 | 0.00503161 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010527 | ACAACAGAACAGTCC[A/C]AGATGGCAGAGGGTA | 114088 |
rs202209972 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025417 | GATACACCAACAAGG[C/T]CAGCGAGACTCAAAA | 114088 |
rs202227387 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049835 | TCTCAAAAAAAAAAA[-/A]TAAAATAAAATAAAA | 114088 |
rs267604001 | snp | C/T | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979514 | AAGTCGAGGAGGACC[C/T]CAATTGTGGCCCCTT | 114088 |
rs267604002 | snp | G/T | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982059 | TGTCATTGGAGAGGA[G/T]GATGTCCGAGTGCGC | 114088 |
rs367547169 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028509 | CTCTGTGCTAACAAA[G/T]ATGTTCTGCATTCAG | 114088 |
rs367565362 | in-del | -/ACACACACACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080437 | ATTGAGTTTTATTGA[-/ACACACACACAC]ACACACACACACACA | 114088 |
rs367573355 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085430 | TGCTTCTATGCAAGG[C/T]TATGAAAAACAGTTT | 114088 |
rs367635868 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978470 | CCCATGCAAGGCCCC[C/T]CATGCCTTAGAAACT | 114088 |
rs367673003 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046269 | AGTTATTATCTTGAC[G/T]GTGTGGTGACTACAC | 114088 |
rs367695979 | snp | A/C/T | 0.000134762 | 0.00820769 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094420 | TGGCTTCCTTGGGCG[A/C/T]CTTCTCGCAGAGCTG | 114088 |
rs367716119 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988686 | CAACAAAAAAATCCT[A/G]CCTTGCAATGAGAAC | 114088 |
rs367724597 | snp | C/T | 3.29919e-05 | 0.00406138 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023001 | CAAGCTGCTGGGTGC[C/T]TCAGGCTGCCAGAGA | 114088 |
rs367753903 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036926 | TGTGTATATTTCTAG[C/T]TGTAATAAACCATTT | 114088 |
rs367754469 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027293 | GGATTACAGCCGTGC[A/G]CCACCACACCGAGTG | 114088 |
rs367763486 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029573 | TCACATTGCTCAGCA[A/G]TTACCCATTGCCGGT | 114088 |
rs367781796 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070603 | CTCTGAAATGCTTCA[A/G]TGAGCATTATCTCTG | 114088 |
rs367787981 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049808 | CCAGCCTGGGTGACA[G/T]AGCGAGACTCTGTCT | 114088 |
rs367881043 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975908 | GTCATAGTAATGACA[C/T]ACAGTCCCATGTTTT | 114088 |
rs367882727 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053580 | TTACTTTTTAATTTT[C/T]TTTTTTTTTTTTTAA | 114088 |
rs367907490 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028947 | GCTCCCCTTGCCTCC[C/G]CAGGAGGGAGAGATC | 114088 |
rs367947996 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053580 | TTACTTTTTAATTTT[-/C]TTTTTTTTTTTTTAA | 114088 |
rs367949855 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040254 | CTTATAATTGACCAA[C/T]AGAAATAGTTGACTG | 114088 |
rs367951792 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985453 | TTATAGGATGCTTTC[A/T]GCTGTTGGTGTGTTT | 114088 |
rs367966623 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052325 | AAAAGAGTCAAGGTC[A/G]GCGAATATAATAAGA | 114088 |
rs367977244 | snp | A/G | 1.65822e-05 | 0.00287938 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009072 | ACTTGGGGGATGCAA[A/G]GACATACCTTTCACT | 114088 |
rs367978624 | snp | C/T | 0.000269109 | 0.0115966 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977276 | ACAGGCAGCTGGCGC[C/T]TCCACGGCACATCCT | 114088 |
rs368069477 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031166 | AAAAAAAAAAAAAAA[A/G]AAAGAAAAGAAAAGA | 114088 |
rs368111570 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089276 | TTATAACTATTTGAT[A/T]CTTAAACATTTATCT | 114088 |
rs368135114 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053050 | CTGTAGTCCTAGCTA[C/T]TCCAGAGGCTGAGGT | 114088 |
rs368158829 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036822 | TTGTTTTTAACTTAA[C/T]CTGACAGTTTTTCCC | 114088 |
rs368202261 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006659 | GACAAAGTGTTAAAA[A/T]AGAAAATGAAAATGG | 114088 |
rs368211836 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031200 | AAAGAAAGAATGATT[A/C]TATCCTTGACCAAGT | 114088 |
rs368252402 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061287 | GCGTGGTGGTGGGCA[C/T]CTGTAATCCCAGCTA | 114088 |
rs368253308 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075970 | ATTTTAATTTTTTTT[-/T]CACTGCTATATTCCC | 114088 |
rs368272803 | in-del | -/AC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008261 | ATGGCATGGAACTAT[-/AC]ACACACACACTGTTA | 114088 |
rs368288648 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067444 | AATCAGATTACATCA[C/T]TCTCCTGCTTAAGAC | 114088 |
rs368327624 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019569 | TAATAACACCAGTGT[A/G]TGAGCTAATTCTAGG | 114088 |
rs368392804 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon | TRIM9 | GRCh38.p7 | 14:50979342 | GGGCAGCCTTTGAAC[A/C/T]GGTAGCCAGCAACAG | 114088 |
rs368405566 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081178 | ACAACCCAATTAAAT[A/G]AGAGCAAAGACTTTA | 114088 |
rs368408575 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053424 | AAAGTTCATTCAGTA[C/G]TCAGTTTGTATCAGT | 114088 |
rs368437164 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074000 | CCTGAAGGCAGCCAT[A/G]GAAAATGCTACAAAT | 114088 |
rs368488415 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047371 | ATTTCATCATGGCTG[G/T]TTCCCACTGGAGCTC | 114088 |
rs368538790 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981187 | GGTAGAAGAAAACCT[A/C]AAGGAGATTACTGTA | 114088 |
rs368551111 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075709 | AATGGAATTAAAAAT[A/G]GCAGCGGGGATGCCT | 114088 |
rs368556117 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993089 | CTCATTTGGTAGTAA[C/T]TTTCATTTGGTAGTA | 114088 |
rs368566267 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006253 | TAGTTTCACAATGGA[C/T]GGATTACTTTAATAC | 114088 |
rs368608695 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067788 | TCCTTACTACTTCCT[A/T]CCAAACACTCTCCAT | 114088 |
rs368614720 | in-del | -/TTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053510 | TCAGAACAGGTATTC[-/TTTTT]TTTTTTTTTTTTTTT | 114088 |
rs368621771 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088294 | GTTTCCAAAGTTAGA[C/G]AAATTTGGAAAATGC | 114088 |
rs368666426 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987622 | TTCTTTCTTCAGATA[C/T]GATAAATCAAAAATT | 114088 |
rs368687430 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035091 | ATGACATGACAAATT[C/T]TGTTGACATATAGAG | 114088 |
rs368711160 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068509 | GTGCCAAGTACTTTA[A/T]GTGGAAAACATCAGT | 114088 |
rs368713100 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059753 | CAGTGAGCCAAGATC[A/G]TGCCACTGCACTCCA | 114088 |
rs368714857 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029050 | CAATTCAATCCATCC[C/T]GCCCAATGCCTGACT | 114088 |
rs368774571 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986501 | AAGAGGATATTATTT[A/T]ACCCCCTTCAGTTGT | 114088 |
rs368786782 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060292 | AGCCTAACTTCCTAT[A/G]ACCATTTAGCTAACC | 114088 |
rs368787760 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010907 | GTGACACTGTCCACC[G/T]TCAGTGCCCTCTACT | 114088 |
rs368829517 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076937 | GCCCAATGCCATTTG[C/G]GCAGTCCCCACTATG | 114088 |
rs368830641 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062066 | ACTGATTCTTTCTGC[C/T]GCTATATCCAGTCTG | 114088 |
rs368909905 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033182 | GCAACCTCCACCTCC[C/T]GGGTTCAAGCAATTC | 114088 |
rs368933566 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090048 | AGTAAGTGGCAGCAT[C/T]GGTTCTATAACCTGG | 114088 |
rs368933785 | snp | C/G | 1.68764e-05 | 0.00290481 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979573 | AAAGAGAAAAATTGG[C/G]GTTCATTTCCTTGTG | 114088 |
rs368994719 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034724 | AATAAATTATAGAGA[C/T]CTATACAGTGACTTA | 114088 |
rs369002549 | snp | A/G | 6.2359e-05 | 0.00558351 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50998011 | CACTTTAGATGCCAC[A/G]CAGTTCTCGCTCTGA | 114088 |
rs369020044 | snp | A/G | 1.65864e-05 | 0.00287974 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979546 | TGTGATCCCTCCCTC[A/G]GTTCTGTAGGAAAAG | 114088 |
rs369041940 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050711 | AATACAGCTTCTGGC[C/T]GGCTTCTTCTCCCTC | 114088 |
rs369046731 | snp | C/G/T | 0.000124093 | 0.00787597 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983345 | TGAGCACACCAATCA[C/G/T]GTAAGTAAAAGATAA | 114088 |
rs369089267 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078409 | ACACTCTTGGATTCA[C/T]GATAGCCAAGATATG | 114088 |
rs369093861 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057251 | TGACTGAGCTAATGA[A/T]TTGTTCTATTACTGC | 114088 |
rs369116570 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995774 | CCAATACCAGCAAAG[-/A]AAAAAAAAATCTCTA | 114088 |
rs369142112 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003690 | CTTCAGATCTTGATA[C/T]TGTCCCAGATTTAGA | 114088 |
rs369174438 | snp | A/C/T | 8.23616e-05 | 0.00641679 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979434 | AGAAGAGGCCCTCCA[A/C/T]GTTATCAAATGCTAT | 114088 |
rs369179880 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040006 | CCAGGATGGTCTCGA[-/T]TCTCCTGACCTCCTG | 114088 |
rs369192084 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020936 | TGCCAGGAAGTGTTC[A/G]CAATGTTTCAAAAGA | 114088 |
rs369265735 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066698 | CACTCCAGTCTGCTG[C/T]GTGGTCAGACAGCAT | 114088 |
rs369284873 | snp | A/G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004320 | TTGAAGAGGTCTGGC[A/G/T]GAGCTGTGGTTCAAA | 114088 |
rs369407588 | snp | A/C | | | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982949 | TTCCATACCTGCCAA[A/C]AGCTTTTTAATGTCA | 114088 |
rs369429059 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050594 | ACAGCAGAGGGTCTA[C/T]GTTTCCCCTCCTCAA | 114088 |
rs369442206 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041052 | GTAATAACTGTCAAT[A/G]TTATTCAGAAAAATG | 114088 |
rs369443106 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017548 | AAGAAATTCAAGACA[C/T]TGGGAGAGAGAAGCA | 114088 |
rs369576835 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004230 | ATTTATCCTTCTTTT[A/G]GCCTGTAAAATCAAG | 114088 |
rs369582921 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016879 | GTTGAATTCATGGAT[A/G]CAAAACCCATGGATA | 114088 |
rs369594912 | snp | A/T | 1.64846e-05 | 0.0028709 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010437 | CCAAGCAGTACTCCA[A/T]GAGACCTGTGGTCTG | 114088 |
rs369619054 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979996 | TATAAATGGTGTGAA[G/T]TAAATATCATTAAAT | 114088 |
rs369627579 | snp | A/C | 0.000102088 | 0.00714377 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094976 | CAGCGACGGCTGCAG[A/C]GGGTGCCTGAGCTGG | 114088 |
rs369630215 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061431 | AAAAAAAAAAAAAAA[-/A]TTGGATTGTTGACTT | 114088 |
rs369652663 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015505 | CTTTCTTTACTTTTC[-/C]TTTTTTTTTTTTTTT | 114088 |
rs369741709 | in-del | -/AAAAC | 0.176861 | 0.239062 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059480 | AATGAAGAGAATGAA[-/AAAAC]AAAACAAAACAAAAC | 114088 |
rs369779237 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982621 | CTCACAAGCTGCGAA[C/G]CTATAAGCAACATAA | 114088 |
rs369881118 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977427 | AGTGTACCGTGGGTG[C/T]GTCCCTAACTCAAAA | 114088 |
rs369905418 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032136 | TGCTGTTTCATTCTT[G/T]GAACCACAAAAAAAT | 114088 |
rs369924677 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066924 | TTCAGTTAGTTTACA[C/T]ACTAAATTAGTCTGC | 114088 |
rs369966597 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093546 | TGGCACCAGGACCCC[A/G]CGTTCTCTCCAGCTC | 114088 |
rs369992097 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022286 | GTTAATTATCATGGG[A/G]GTGGGCTCCCAATAA | 114088 |
rs370016549 | snp | C/T | 6.60426e-05 | 0.00574604 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022804 | AGCCTGGCTTGTTGG[C/T]TTTCTGCTCTTCCCA | 114088 |
rs370055388 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060668 | GAAACGGGGTTTCGC[C/T]GTGTTAGCCAGGATG | 114088 |
rs370079075 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014030 | TTGACTACAGGTACT[A/G]GAAGTCCGAATAATA | 114088 |
rs370088505 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026075 | CCAGCCTCCTCGTCC[A/G]CTGGGGAGGCCGTGG | 114088 |
rs370163214 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049255 | ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCAAGTT | 114088 |
rs370245065 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033047 | ACTACTGGTCCTAAT[C/T]ATTCTGGATAAGAGA | 114088 |
rs370254907 | snp | A/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979016 | AGTCTTACACCCTCA[A/C]CTCTTCTCAGGCACT | 114088 |
rs370288904 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085476 | AAATCCATTCTTAAA[C/T]GATATCCTCCTCGGT | 114088 |
rs370302150 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015505 | TCTTTCTTTACTTTT[C/T]TTTTTTTTTTTTTTT | 114088 |
rs370305965 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012085 | AATATACACAGCATG[A/G]CATTTTCCACTGTAA | 114088 |
rs370423015 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061415 | AAGACTCTGTCTCAA[A/G]AAAAAAAAAAAAAAA | 114088 |
rs370455492 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073605 | CAAAGTTACCATGCT[G/T]CTAGAAGGTTATCCT | 114088 |
rs370486293 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005646 | ACAACCTTAGAATTA[A/G]GTGGAAAATGTTTTT | 114088 |
rs370491659 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087019 | AAACACAGCTGGGGT[C/G]GGGGGAGGTGGCGGG | 114088 |
rs370508371 | snp | A/G | 8.23649e-05 | 0.00641683 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981956 | TCATAGCGATCTACC[A/G]TGAGCTCCCAGTAGT | 114088 |
rs370533877 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055064 | CTTGACCTCGTGATC[C/T]GTCCGCCTCGGCCTC | 114088 |
rs370608455 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998414 | GTGTGAGGATTACTT[A/T]ATGTTGTATATGCAG | 114088 |
rs370656784 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094181 | GTGTTTGCCCTCCTC[C/T]AAGCACTGGTAGCAC | 114088 |
rs370664137 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991831 | GGCTAAGGGACATAT[C/T]CAAGTTACACCACAG | 114088 |
rs370674537 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051366 | CAGTTATTCTTCATT[C/G]CCTCTCTCTTTGGCC | 114088 |
rs370694389 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070251 | CATGAGTTATAGTGC[A/G]ATGGCTGTGAGTTCA | 114088 |
rs370697124 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021633 | TTCATCCTAATGCCA[G/T]ATCAACACTGCACAC | 114088 |
rs370709233 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090421 | CATATTAACTGACAG[G/T]TTATTTTAAAATATT | 114088 |
rs370764204 | snp | A/C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992017 | GGGACCAAGGTTTGT[A/C/G]TAGAGGACCTAATAA | 114088 |
rs370824286 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084124 | AGTTTTAGTAAGAGT[C/T]TTTATATCTAAATGT | 114088 |
rs370875493 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030741 | TCAGTGGAGTATGGG[A/G]AGGCTCTTGGCTTTG | 114088 |
rs370875557 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021062 | CAAAGACATTTGTGG[C/T]TTTATTTTATACAGT | 114088 |
rs370887740 | in-del | -/TT | 0.489259 | 0.0724914 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013227 | AAGTGTCTAACTTCA[-/TT]TTTTTTTTTTTTTTG | 114088 |
rs370909987 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072753 | GCATTCGTACTGTTT[A/G]CACTTAAGAACCTCT | 114088 |
rs370943141 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, splice-donor-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981852 | GGTTATTGTCCACAT[A/G]CATTGCCCAAGCTTT | 114088 |
rs370953538 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060848 | TATTGCTGAATAGTA[G/T]TCCATTAACTTTATG | 114088 |
rs370963907 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012211 | AATTGAAACTCTAAA[C/T]CCATTAAACAACATC | 114088 |
rs371014339 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032808 | AGTTATATGCAATGC[C/T]TAGCATATTGTTAAA | 114088 |
rs371023280 | snp | C/T | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974894 | GTAGTCCCAGCTACC[C/T]GGGAGGCTGAGGCAG | 114088 |
rs371053298 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012629 | AATTTTTTGAGGGAT[C/T]ACCATACTGTTTTCC | 114088 |
rs371061563 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033299 | GGTTTCACCATATTG[A/G]TCAGGCTGGTCTTGA | 114088 |
rs371074403 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067706 | GCCCCTTCTCATCAC[C/T]ATTTAGGTCTCAGTT | 114088 |
rs371076513 | snp | C/T | 3.347e-05 | 0.00409071 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009032 | TGCTTCAAGCACCAG[C/T]ATCCACTCAGGATGT | 114088 |
rs371085768 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064914 | TTGAAATCATTATAA[A/G]TCATAAATAAAGCTT | 114088 |
rs371113088 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027668 | TTATGATTGGGTCTC[A/G]GCTACAATATTATTT | 114088 |
rs371142881 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009425 | TCAAGCAAATCTGAA[C/T]ACTTTTGTGAGTTGG | 114088 |
rs371193891 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001450 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 114088 |
rs371229982 | snp | C/T | 0.00398564 | 0.0444627 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975436 | ACTATGAGTCTACCA[C/T]GGCCCAGCCATTGAG | 114088 |
rs371296126 | in-del | -/ATA | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079229 | TTAGAGAGTGAAACT[-/ATA]ATAATAATTGAACTA | 114088 |
rs371304515 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071389 | CTAAAAAAAAAAAGA[A/G]AAAAAAAAAAAAAAG | 114088 |
rs371319328 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005315 | ATTCAACTTGAGTCA[A/C]TAAAAATAAATACAC | 114088 |
rs371337165 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026791 | CTCGCTCTATCCCCT[A/G]TAAGTGTGACCTTGA | 114088 |
rs371341237 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026087 | TCCGCTGGGGAGGCC[A/G]TGGTACACAATCCTG | 114088 |
rs371419261 | snp | C/T | 1.83791e-05 | 0.00303137 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977376 | ATGAGACTGTGAGTC[C/T]TGAGAGGCATCGTGC | 114088 |
rs371493448 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986376 | AGGCAATTGTTGTCA[A/C]TTTCCCGATTTTTAG | 114088 |
rs371541690 | in-del | -/AT | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044131 | GTACTAGACTGTAAC[-/AT]GTGATTTTACAGAAA | 114088 |
rs371542917 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016129 | GGCATATTACCTATG[C/T]ACATCCTCTTATATA | 114088 |
rs371551146 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071387 | GTCTAAAAAAAAAAA[-/G]AAAAAAAAAAAAAAA | 114088 |
rs371570089 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061782 | GTTTTAGCAGCATTT[A/T]TCCTACTCAGGGTTC | 114088 |
rs371575605 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070832 | TCCTGTGGACCAAAT[A/G]TGCACATCTTGCTTG | 114088 |
rs371604441 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095005 | GGCGAGGTGGCCGAC[A/G]GGCCCGTCTTGTCCA | 114088 |
rs371645942 | snp | A/G | 3.39564e-05 | 0.00412032 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094349 | CCCCCGGGGCGGGTG[A/G]CAGCGCAGGCGGCAC | 114088 |
rs371666425 | snp | C/G | 0.000160352 | 0.00895267 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982138 | ATCAGGTTATTAAGA[C/G]AGACCCAACAAGCTC | 114088 |
rs371672401 | snp | G/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096335 | AGGGAAGAAAGGGAG[G/T]GAGGAAGAAGAAAAG | 114088 |
rs371690616 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025420 | ACACCAACAAGGCCA[C/G]CGAGACTCAAAACTG | 114088 |
rs371691143 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093106 | GAGGCAATGAGGTCG[A/C]AGGGGCCAAAATGGA | 114088 |
rs371700748 | snp | A/C | 0.000347939 | 0.0131852 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009028 | ATCCTGCTTCAAGCA[A/C]CAGCATCCACTCAGG | 114088 |
rs371718043 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021999 | AAAACACATTTTTTT[-/T]GCCTGTGTATGGCCA | 114088 |
rs371754337 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031218 | TCCTTGACCAAGTTA[C/T]AGCCAGGGTCCTCTG | 114088 |
rs371767938 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078429 | GCCAAGATATGGAAA[C/T]AACCTAAGTGTACAC | 114088 |
rs371824086 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979929 | TTAAAGACTAGGAAA[A/G]AGTCGCCTTTGGGCT | 114088 |
rs371830157 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038018 | TCTGCTTCTTGATGC[C/T]GTAGGCAAAATAATG | 114088 |
rs371844014 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011192 | CATTTGCCAAGCTGT[A/G]AGTCTGCTTTAACCT | 114088 |
rs371876907 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059613 | GACCAGCCTGACCAA[C/T]AGGGTGAAACCCCAT | 114088 |
rs371882873 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041040 | ACAACAAAATTAGTA[A/C]TAACTGTCAATATTA | 114088 |
rs371891253 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088795 | TCTGCTTCATTGAAT[C/T]AAAAACCGCCCCTCT | 114088 |
rs371891918 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053593 | TCTTTTTTTTTTTTT[-/A]AATTTTTTTTTTTTT | 114088 |
rs371942257 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004291 | CAAGGGGGAAGCTAT[A/T]CTCACTGACTTCCTT | 114088 |
rs372002032 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046208 | TAGAGATAAGTAGGT[A/G]TGGTTACAATAGGGC | 114088 |
rs372043867 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014037 | CAGGTACTGGAAGTC[C/T]GAATAATAAGGACAG | 114088 |
rs372059906 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990292 | CCAGTGTTGAGATTA[C/T]AGGCATGAGCCATGG | 114088 |
rs372070122 | snp | C/T | 8.25675e-05 | 0.00642471 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025229 | CAGTTACGTATTAAC[C/T]GGCGGGTTTCCTTGC | 114088 |
rs372070978 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982629 | CTGCGAAGCTATAAG[C/G]AACATAAACTAATTT | 114088 |
rs372086608 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989766 | GTTCGTAACGAATAC[A/G]TATCAAGATATGCTT | 114088 |
rs372089654 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999023 | ATATTATGTCCTCTC[A/G]TTCAGTGCTTCTCAA | 114088 |
rs372097575 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976731 | GAGTAGTAAAACTTC[G/T]CAGTGATAGATTCAT | 114088 |
rs372108643 | in-del | -/AAT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001540 | GGCCGCTGTGCTAAT[-/AAT]TTTATCATAAAACTT | 114088 |
rs372118611 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071330 | GTGCTGAGCCGAGAC[C/T]GCGCCATTGTATTCC | 114088 |
rs372123445 | in-del | -/T | 0.281577 | 0.247998 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002289 | ACCACGGCTGGCTGA[-/T]TTTTTTTTTTTCTTT | 114088 |
rs372141690 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093685 | CCGCCGTCCGCGCGA[A/C]CCCACCGCCCCCATC | 114088 |
rs372156723 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044106 | TTAAAAATTTAAAAA[A/C]TTTGCACAAGTACTA | 114088 |
rs372257296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986532 | CCTGGGAGTTACTAC[C/T]TATTCAACAATGGCC | 114088 |
rs372296103 | snp | A/G | 0.000153988 | 0.00877328 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979353 | GAACCGGTAGCCAGC[A/G]ACAGCTGTTTAACCT | 114088 |
rs372339004 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068346 | AAACAAAAACAAAAA[A/C]AAAAACAAAAAACAA | 114088 |
rs372350250 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053128 | TTGTGCCACTGCATT[C/G]CAGCCTGGGTGACAG | 114088 |
rs372350713 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028159 | AAGCAGTAAGTGAAC[-/T]GCAAAAATCAATTTA | 114088 |
rs372371219 | snp | C/T | 0.000421965 | 0.0145191 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977395 | GAGGCATCGTGCATC[C/T]CCCTGTCCCTTTACA | 114088 |
rs372398911 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059311 | AATTGTGGAAGCAGA[C/T]AGGCTAGCATTTACC | 114088 |
rs372540375 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001322 | GCAAGCTCCGCCTCC[C/T]GGGTTCACACCATTC | 114088 |
rs372593890 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979454 | TCAAATGCTATGGGA[C/T]CTTGTTGTTCATCGT | 114088 |
rs372619396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059474 | GGAGCACAATGAAGA[A/G]AATGAAAAAACAAAA | 114088 |
rs372619774 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068433 | AGATCTCACAAGGGG[-/A]AGATAAAATAAGAAT | 114088 |
rs372624818 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050268 | ATGTGTTGTGGGAGG[C/G]ACCTGGTGGGAGATA | 114088 |
rs372658120 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062196 | CACTCAACTGTTTAT[A/G]CATGTTATTCAACTT | 114088 |
rs372677234 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050128 | CATATGGCCATAGGA[C/T]ACCCTTCTTACAGAA | 114088 |
rs372711926 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011914 | TCATGTTGCCACAAC[A/C]AATGGTTACAAAAAT | 114088 |
rs372734393 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041079 | AATGAATTTAAGCCA[C/T]GTCTGATTTCTTTTC | 114088 |
rs372736328 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086809 | GACAATCAGGTACAA[A/G]CAGGAATTGAAACCA | 114088 |
rs372743437 | snp | A/G | 0.000463653 | 0.0152188 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000663 | TGGGTTAACAAGTAC[A/G]TAGTGGGCTGTCTAC | 114088 |
rs372767327 | in-del | -/CAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068354 | CAAAAACAAAAACAA[-/CAA]AAAACAAACCCAAAT | 114088 |
rs372828177 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076475 | CATAAGCATTTCAGC[C/T]GTTCTTTCCATGCTT | 114088 |
rs372834409 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063758 | CCTTCAAAAATTAAC[A/G]GAAAAGAAAGACATT | 114088 |
rs372855487 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087725 | ACAAGCATTTACTTC[A/G]TAAGTTGTTATGCTA | 114088 |
rs372880123 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008537 | CCACCCAGAATCTCA[A/G]AGAGACCTTGCCATA | 114088 |
rs372889784 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028217 | TCCGTCCCAAGAATG[C/T]CTTCTACCTGGCTGA | 114088 |
rs372897239 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059100 | CCAATATCAGCACGA[C/G]CTTCCCTGCTTTGCC | 114088 |
rs372914600 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087210 | GGAGGGCAAGCGTAG[A/T]GGACAGGAAGGGAGG | 114088 |
rs373061701 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998050 | GCTGAAGGGCCTTAC[C/T]CTCAGACGTTTGGAG | 114088 |
rs373069440 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062698 | GCTGGAAATTGAGAG[A/G]GGAATCCTTGAAATC | 114088 |
rs373086477 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005449 | AACAAACTGGCATTT[C/T]ACTTCAGTACCATGA | 114088 |
rs373086888 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980139 | ATTCCAGAAGGATAG[A/C]AGTTTTTTGGCTTGT | 114088 |
rs373089056 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995458 | TAGACAGATAAATTT[G/T]CTTTCGAAGAAAAAA | 114088 |
rs373160493 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977089 | TGTTGGACATGGAAG[C/T]GGAAGCAGGCATGAC | 114088 |
rs373182264 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020904 | TCGCAAACTGTTCAC[A/C]ATGTTCTGTTAAAAA | 114088 |
rs373190057 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980501 | GTTTACAAATTGCCT[C/T]TTGCTACTTCACAGG | 114088 |
rs373260739 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991027 | TTGCAATTGAGAAGT[A/G]AGAAACAAATCTGTT | 114088 |
rs373329873 | snp | A/T | 1.73402e-05 | 0.00294445 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094091 | CGGAGACGCAGGGAG[A/T]TAGGAGTGGGTTTTC | 114088 |
rs373388647 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073643 | AGTGTGGTGTGGGCG[C/T]TCTGGACTGGAAGGG | 114088 |
rs373440593 | snp | C/G | 0.00279162 | 0.0372561 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095499 | GGCTGGGGCTTCTCG[C/G]CAGCGTTTGCGTTTG | 114088 |
rs373477270 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011498 | AATGGTTTTTGAAGC[A/G]TAAAATTGAAGAAGG | 114088 |
rs373493628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075096 | CGCTAACTGGGACCT[C/T]AGCTCTCATGTAATC | 114088 |
rs373565283 | snp | A/C/G | 0.00102033 | 0.0225641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982108 | AAACCAGGCCACTGG[A/C/G]AACAACAGAAGGGAA | 114088 |
rs373682663 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083430 | CAGCTAATTAAAAAA[A/T]ATTTTTTTTTTAGAG | 114088 |
rs373699570 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052654 | GCAGAGGCGGCCAAA[A/T]TTCTATAACATTCAG | 114088 |
rs373701836 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085429 | CTGCTTCTATGCAAG[C/G]CTATGAAAAACAGTT | 114088 |
rs373712567 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030757 | AGGCTCTTGGCTTTG[C/G]GGGAGGCTCTTGGCT | 114088 |
rs373720426 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073641 | AGAGTGTGGTGTGGG[C/T]GCTCTGGACTGGAAG | 114088 |
rs373724799 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986408 | GGTAGAAAATTGGAA[C/G]GTTTCCTTTTAATTA | 114088 |
rs373727917 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033150 | GCTGGAGTGCAGTGG[C/T]ACGATCTCAGCTCAC | 114088 |
rs373776847 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032540 | ACAACCCTGAAGAAC[C/T]ATCCCAGATCTAGAA | 114088 |
rs373786798 | in-del | -/AAAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031176 | AAAAGAAAGAAAAGA[-/AAAG]AAAGAAAGAAAGAAA | 114088 |
rs373790230 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051689 | AAGATGGAATAGGCC[A/G]GGCGCAGTGGCTCAC | 114088 |
rs373831398 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051165 | ATGTTCTGGTTCACC[A/G]GTTACAAAAAAATAT | 114088 |
rs373832461 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012857 | CTGTTTGTGTACCCT[C/T]GCTGCTAATCAGGTC | 114088 |
rs373901644 | snp | A/G | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975194 | TGAGATCTTCCTGAA[A/G]AAACATCGCTCTGAC | 114088 |
rs373998163 | snp | C/G | 0.227369 | 0.248974 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031908 | ATATACTAAACAAAT[C/G]TCACCATTTGTATTG | 114088 |
rs374038423 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028897 | CTCCTTCCCTCCTTG[C/T]GTGGCTTTCGTCCTC | 114088 |
rs374114307 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042347 | CAGTCTCCTCTTCCT[C/T]CCTCCTCTCAAAGCT | 114088 |
rs374121481 | snp | A/G | 0.000307953 | 0.0124049 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981948 | GGTGGTTGTCATAGC[A/G]ATCTACCGTGAGCTC | 114088 |
rs374220262 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049435 | CAGGGCTGCCACGAT[G/T]GCTCAGCACAACTCA | 114088 |
rs374307772 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077591 | TAGAGATGGGGTTTC[A/G]CCATGTTGACCAGGC | 114088 |
rs374315245 | snp | A/G | 1.64988e-05 | 0.00287213 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000851 | GGAAGCTAAACAGAA[A/G]TTAGTGTAACTCTGG | 114088 |
rs374347048 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078761 | GGAGAAAATGAAGGA[C/G]ATGTAAGTCCAATAA | 114088 |
rs374352912 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093887 | CGCGCCCCGAGAGAC[C/T]CGCTCTAAGGCATCC | 114088 |
rs374361255 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080386 | TGGGTGTCTGAGGGC[A/C]TGGAAGAGTCCCCAG | 114088 |
rs374384976 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041419 | TTTGAGCTGCAGCCC[A/T]CTCTGCTCCTCGCCC | 114088 |
rs374409574 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085964 | TAGGCCTATACCTCC[A/G]ATGATCTGGTCTGTG | 114088 |
rs374421732 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062129 | TGATATTGTGCTTTT[C/T]ATTTCTAGTATTTAC | 114088 |
rs374460582 | snp | A/C/T | 0.000150224 | 0.00866542 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009045 | AGCATCCACTCAGGA[A/C/T]GTTGCTCTCTGACTT | 114088 |
rs374465844 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046132 | GACAGTTTAGTAGTA[C/G]CCAGGGATTAGGGAT | 114088 |
rs374473525 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081030 | TAAGATTTCCTCCCA[C/T]GCAGGTCTGTGTCTG | 114088 |
rs374538926 | snp | A/C | 1.64982e-05 | 0.00287208 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022811 | CTTGTTGGCTTTCTG[A/C]TCTTCCCATGATGCA | 114088 |
rs374555865 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005175 | TTAACAGATTACATG[A/C]AAGTGTGTGTGCTCA | 114088 |
rs374585794 | snp | A/C | 0.000221117 | 0.0105123 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025412 | CACAGGATACACCAA[A/C]AAGGCCAGCGAGACT | 114088 |
rs374602884 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065865 | GGTGCTTTGACATTT[A/G]TAAGTGAGTTTACAC | 114088 |
rs374603725 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055073 | GTGATCCGTCCGCCT[C/T]GGCCTCCCAAAGTGC | 114088 |
rs374608701 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043124 | TTGTGACAATTGTCT[C/T]CCCAAATGTCTTGTA | 114088 |
rs374638795 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995602 | CCTCAGACTAAATGC[-/A]TGTGATTACAAGTTA | 114088 |
rs374682468 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060782 | TATATTCATTCTCTT[A/G]TAAGAAGCAGATTGA | 114088 |
rs374695140 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975592 | AGAAAAAGATTGTAA[C/T]TGATAGAAATAATCT | 114088 |
rs374758082 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053596 | TTTTTTTTTTTTTAA[-/T]TTTTTTTTTTTTTAT | 114088 |
rs374780531 | snp | C/T | 1.65081e-05 | 0.00287293 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979526 | ACCCCAATTGTGGCC[C/T]CTTTTGTGATCCCTC | 114088 |
rs374799105 | snp | A/G | 1.78573e-05 | 0.00298803 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977283 | GCTGGCGCCTCCACG[A/G]CACATCCTTAGGCTA | 114088 |
rs374837100 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048197 | TAAACAGTTTCCTAA[A/C]AGCTTTGGGAAAATT | 114088 |
rs374869984 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034333 | CCTTAACTAGGAAAA[C/G]AGCAATAAGAAGTTT | 114088 |
rs374883806 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093944 | ACTCCCCCGTGCGCC[A/G]GTTAAGATTCCCCCA | 114088 |
rs374906533 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046441 | TGGTTTTGCAAAATG[C/T]TACCACTGGGAGAAA | 114088 |
rs374921511 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071582 | AGGTGGTAGGATGAT[C/T]GCTTGAGCTCAGGAG | 114088 |
rs374955524 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068200 | ACTAGTATTTACTAA[C/T]TGCCAAGTATCTTCT | 114088 |
rs374962274 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054163 | AGCTCCTGGGCTCAA[A/T]CCATCCTCCCACCTC | 114088 |
rs374989373 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046236 | GGCAACGCAAGGGAC[A/G]CTTGTGGGGCTGGAC | 114088 |
rs375036719 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041041 | CAACAAAATTAGTAA[C/T]AACTGTCAATATTAT | 114088 |
rs375053094 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997320 | TATTTAAAGTATAGC[C/T]AAGAAGCAAAAATTC | 114088 |
rs375053833 | snp | A/G | 4.94181e-05 | 0.00497057 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979399 | TACCTGCACGTTCCT[A/G]TTCAGGCTGACCGCA | 114088 |
rs375104843 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036871 | GGGCTATCTACATCT[A/G]TTGTGTTAACTGACA | 114088 |
rs375143107 | snp | C/T | 0.030278 | 0.119257 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061344 | CTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 114088 |
rs375168374 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056316 | AATTAAAAAAATAAA[C/T]TCATTGTGTTAACTG | 114088 |
rs375218495 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093141 | GTCATGTAGGACAGG[C/T]TGAGAAGCGTGGGAA | 114088 |
rs375237204 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992064 | GGATACATCTTTTCT[G/T]CTTTAAATAGAGTGT | 114088 |
rs375254437 | in-del | -/ATT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091130 | TTGACTTATAAGACC[-/ATT]ATTATTATTATTATT | 114088 |
rs375289135 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986852 | GTAGGCAGTGGTGAG[G/T]TGCATTGGTGGCAAA | 114088 |
rs375301193 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985614 | ACATTACTGCCATGG[-/C]CCGCCACTCAGCCAG | 114088 |
rs375315674 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981590 | TACAGCAATGAAGGG[A/G]GTAGGAAAGTACTCA | 114088 |
rs375321483 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068355 | CAAAAACAAAAACAA[A/C]AAACAAACCCAAATC | 114088 |
rs375333472 | snp | C/T | 0.00208024 | 0.0321837 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000737 | GTATCCATCGGCGGG[C/T]ACCGTGGACAGAGGT | 114088 |
rs375334176 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053249 | AATCTTAAAAAATGT[C/T]TTACACAGAGCACTT | 114088 |
rs375347675 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017208 | CACCACTCTCCCTCA[C/T]AGTTTAAGGCAAATA | 114088 |
rs375366364 | in-del | -/TT | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013241 | ATTTTTTTTTTTTTT[-/TT]GCATGTGGATATCCA | 114088 |
rs375388629 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009878 | ATCCAGCTTACACCA[C/T]AGCATCTCACTAAAA | 114088 |
rs375406516 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086555 | TTATCTAACTTCTAC[A/T]AAGTACAGAAACGGA | 114088 |
rs375413789 | snp | A/G | 0.00258387 | 0.0358505 | intron-variant, synonymous-codon | TRIM9 | GRCh38.p7 | 14:50979309 | GCTTCCCTCTCTTCG[A/G]TTGGATTGAACGGCC | 114088 |
rs375427514 | in-del | -/AGTA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067277 | CTCTTTTGTACTGTA[-/AGTA]TCTTCCAAATATAAG | 114088 |
rs375538699 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976536 | GTCAATAGTAGGTTC[G/T]CAATTAAAAGCTTTT | 114088 |
rs375545232 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991578 | CATTTCCTTATATGA[C/T]CCTTTATCAATCATT | 114088 |
rs375570499 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058660 | CCACAGCTGCCTAGA[C/T]CTCCAAGGATGGCTT | 114088 |
rs375570930 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997825 | TCAAAGGAAGCCGCC[A/G]GCCCAAGCCATTGGA | 114088 |
rs375580552 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045825 | TGGTCATTAAAGACA[G/T]ACCTCAATTCAAGTG | 114088 |
rs375584120 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026085 | CGTCCGCTGGGGAGG[C/T]CGTGGTACACAATCC | 114088 |
rs375607498 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067656 | GCTATTTCATCTGTT[C/T]GGCTGGCCCTTCCTG | 114088 |
rs375642039 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007799 | GCAACACATATTAAA[-/C]CAAAAAAAAAAAAAA | 114088 |
rs375653864 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012675 | TTTTACATTCCCACA[C/G]CAATGCACAAGGGTT | 114088 |
rs375667432 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074269 | ACAAAAAAAAAGTAA[C/T]GGAAAAAAATTCAAA | 114088 |
rs375676121 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088060 | TAATTATTTTTACCT[A/C]TTTGACTTTTAATGT | 114088 |
rs375676867 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053160 | GAGAGACCCTGTTTC[-/A]AAAAAAAAAAAAAGA | 114088 |
rs375683259 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049423 | GCACATCTACTACAG[C/G]GCTGCCACGATTGCT | 114088 |
rs375689086 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080289 | TAGTATAGACATATA[A/T]AACTTCCCCTTAAAG | 114088 |
rs375714579 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093542 | CACGTGGCACCAGGA[A/C]CCCGCGTTCTCTCCA | 114088 |
rs375724132 | snp | C/T | 0.000118791 | 0.00770592 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094826 | CTCTGGGGTCTGCAC[C/T]AGGATGTTGCGGGCG | 114088 |
rs375729825 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048616 | TGTGCTTTCATAGGT[A/G]TGTGTCTAGGGTGTC | 114088 |
rs375772356 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049942 | GTGTGGCTGGAGGGG[G/T]TGGGTGCATTAAGAG | 114088 |
rs375793408 | snp | A/G | 6.5962e-05 | 0.00574253 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009093 | ACCTTTCACTTGCAC[A/G]AAATCCAGCTGGTGG | 114088 |
rs375809310 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050542 | TCAGCAGCATGGGAA[C/G]AGACTAATACAATGT | 114088 |
rs375811326 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017422 | TGTGAAATTTCTATT[C/G]TAGAAGTGTGAATAT | 114088 |
rs375820715 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998813 | ATCCTAGCATAATGC[A/G]TCTTTAGCATAGGTT | 114088 |
rs375876823 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991878 | TAGAGACTCAGGTAG[G/T]ATCAATTCCTGGAGG | 114088 |
rs375896448 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033016 | ACCAGAATCTGCAAC[A/T]CTCAAAATCTGAAAC | 114088 |
rs375905066 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022061 | TACTCACCATCCTCT[C/T]TTCCTACTTTTAGAA | 114088 |
rs375906658 | in-del | -/G/GG | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096301 | AAGGAAGGGGGGGGG[-/G/GG]AAAGGAAAGGCGGAA | 114088 |
rs375910204 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038405 | TGGCAGCAATAGAAA[C/T]CTAACACACCTGAGA | 114088 |
rs375931729 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013637 | ACTCTGATGGAAAGA[G/T]TATTTTTGTGAGTTT | 114088 |
rs375935388 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040055 | CCCAAAGTGCTGGGA[C/T]TACAGGCGTGAGCCA | 114088 |
rs375956653 | in-del | -/AG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071386 | CGTCTAAAAAAAAAA[-/AG]AAAAAAAAAAAAAAA | 114088 |
rs375989243 | snp | A/C | 8.31414e-05 | 0.006447 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998230 | CACTTAGCCTGCCCC[A/C]TTCTGAGGGGCGAGG | 114088 |
rs375992413 | snp | C/T | 2.43046e-05 | 0.00348593 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997998 | CGGGCTTGCCAGCCA[C/T]TTTAGATGCCACGCA | 114088 |
rs376053676 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980296 | CCATTTTACAAAGAA[C/T]TGTGTCTTATGCTTC | 114088 |
rs376096245 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011677 | TCATTTTTGGTTATA[A/C]ATTTATTTTCCATTA | 114088 |
rs376171074 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097157 | TGCAGTGTTGGGTTC[A/G]CAAAAAGAACAACAC | 114088 |
rs376181470 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012017 | CTAATATTTTGACAA[C/T]TCATTCATTCATTAT | 114088 |
rs376210523 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980552 | TGACATGCAGGTTGC[A/G]TGCAAGCAGATGTGT | 114088 |
rs376266809 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075814 | CCACCTTCTGACTAA[C/T]CCAACTTCTGCCTTT | 114088 |
rs376372249 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026753 | GATGGTAGAAAGAAT[A/G]TAGGTTTGAAAGGGT | 114088 |
rs376396262 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024055 | CTAAATTTTGGCTTT[C/T]ACGGCAATTGCTTTT | 114088 |
rs376401974 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027304 | GTGCACCACCACACC[A/G]AGTGAACTTTTGTAT | 114088 |
rs376432613 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990148 | TCAGCATCCTGAGTA[A/G]CTGGAACTACAGGTG | 114088 |
rs376448569 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067345 | CCTAGCCACCATCAC[A/C]TCTCTCCTGGACCAC | 114088 |
rs376455654 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020055 | AATACACACACAACT[C/T]CTCTCTTTGTCAGCA | 114088 |
rs376461123 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975479 | GTAAATCAAATATCA[A/G]ACTAGTGTTGCCCTG | 114088 |
rs376463315 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045499 | TCAGTTGGAGTATTG[A/T]AGAGGGCATTTAAGA | 114088 |
rs376465173 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095774 | TGCGTCCCTCGTTTC[C/T]TAAAGAGCATGTATA | 114088 |
rs376507696 | in-del | -/CTTCTCCG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038766 | TCACCAAGAGTGAAG[-/CTTCTCCG]TCAGTCTGGAATCAA | 114088 |
rs376582628 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034480 | TAGAGTGACATACAG[A/G]AAAGAAGTACATTCA | 114088 |
rs376618466 | snp | C/T | 8.48529e-05 | 0.00651301 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010534 | AACAGTCCAAGATGG[C/T]AGAGGGTAGAAGAGA | 114088 |
rs376623771 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002406 | CCCAAAGTGCTGGGA[A/T]TAGAGATATGAGCCA | 114088 |
rs376644342 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083301 | TTTGTCACCCAGGCT[A/G]CATGCATTGGTGTAA | 114088 |
rs376728307 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062847 | TATCTGCATCTGCCA[A/T]GTGAAGAGGAGTTAG | 114088 |
rs376783826 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072598 | AAACTTTCTAAAATT[C/T]ATGTTTAATATGAAA | 114088 |
rs376795391 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977107 | AAGCAGGCATGACAG[C/T]GGAGGAGAGGTTGAA | 114088 |
rs376891275 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070111 | CATTTTGGTGCTTTT[-/T]GGTGGTGCATTTGCT | 114088 |
rs376920392 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997846 | AGCCATTGGAACTGC[C/T]GATGTGGAATCTTTG | 114088 |
rs376930469 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026086 | GTCCGCTGGGGAGGC[C/T]GTGGTACACAATCCT | 114088 |
rs376938454 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090122 | AGGAATAACTGTCTT[C/T]TCTGTAACATTTTCC | 114088 |
rs376939493 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069563 | AAATCCGAGGCCCTC[A/G]GGACAAGCCAGGCAT | 114088 |
rs376982727 | snp | G/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997179 | CACAAATACCTCCTT[G/T]TAGGTTTAATTTCAT | 114088 |
rs377012408 | in-del | -/AAGAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035046 | AACACATTAAGTGAA[-/AAGAA]CAGATTTCAAGATAG | 114088 |
rs377015107 | snp | A/G | 3.30246e-05 | 0.0040634 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022802 | GGAGCCTGGCTTGTT[A/G]GCTTTCTGCTCTTCC | 114088 |
rs377017804 | snp | C/T | 0.000153988 | 0.00877328 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000861 | CAGAAATTAGTGTAA[C/T]TCTGGCTTCTGTTAA | 114088 |
rs377044963 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091530 | TGGAGATAGAAGTAC[C/T]ATTAACTAAAACATA | 114088 |
rs377103808 | snp | C/T | 4.94271e-05 | 0.00497102 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000814 | CCTCCAGCTGTAGGA[C/T]AGGGGTTGCTGGGAC | 114088 |
rs377172184 | snp | C/T | 0.000191969 | 0.00979529 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094961 | CGGTCTGGGAGGAGA[C/T]AGCGACGGCTGCAGC | 114088 |
rs377177534 | snp | C/T | 1.65113e-05 | 0.00287322 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010378 | CAGAAACTAGTTAAC[C/T]CTTACCTGCAAAAAA | 114088 |
rs377261251 | in-del | -/AGCTGCC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058649 | TGGCCCCAAGACCAC[-/AGCTGCC]TAGACCTCCAAGGAT | 114088 |
rs377286235 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007832 | AGGACAAAATAAGAG[A/G]GAGCAAAAATCCATT | 114088 |
rs377300663 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044526 | CCTTTCCCCATTTTA[G/T]TCTTTCTGCCCTCTG | 114088 |
rs377304350 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031956 | GCTGTGTGGAGGGCA[A/G]AAAGGAGGAGGGCTC | 114088 |
rs377307373 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020913 | GTTCACCATGTTCTG[A/T]TAAAAAGTGCCAGGA | 114088 |
rs377311671 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066785 | CTCCACTGGTTGCAG[A/C]TCGGCGTTTGCCTTA | 114088 |
rs377311782 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078432 | AAGATATGGAAACAA[A/C]CTAAGTGTACACCAA | 114088 |
rs377354262 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991432 | TTTACCCAAATATGG[C/T]CAGGTATGATTACCT | 114088 |
rs377371893 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094175 | GCTGGAGTGTTTGCC[C/T]TCCTCCAAGCACTGG | 114088 |
rs377408776 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987191 | AATAATAATTTTGTT[A/T]CTGTGACCAGAGGGT | 114088 |
rs377420900 | snp | C/T | 4.98409e-05 | 0.00499179 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981765 | CTGATCAGAAGCCAA[C/T]GTGAAGAAGGCTTGG | 114088 |
rs377446070 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030716 | ATGTGATTGTATGTG[A/C]GATATGTCATCAGTG | 114088 |
rs377446839 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060640 | CCCGGCTAATTTTTT[-/T]GTATTTTTAGTAGAA | 114088 |
rs377475043 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012285 | TTCCTTTCTCTATGA[A/G]TTTCACTATGCTAAG | 114088 |
rs377475313 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036568 | TCTAGATTACTTATA[A/G]TACCTAATACAATGT | 114088 |
rs377577305 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027641 | AAAGTGAGCCTACAG[C/T]TGCAAAATTCTTTAT | 114088 |
rs377617253 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090273 | AGACTATATTGTGTT[A/T]ACTGCTGACATATAG | 114088 |
rs377665073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062938 | CTAACAAAGTAGAAT[A/G]CTAAGCCACATGAGA | 114088 |
rs377665374 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079287 | TTGGCCAATCTTTGG[C/T]TAGCCTCCAAATTGA | 114088 |
rs377700434 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005194 | TGTGTGTGCTCATTC[C/T]ATCCCCGCTAACCCT | 114088 |
rs377709080 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042189 | CTGGTTTTTCAAAGC[C/T]GTTGCAAGTATGTGA | 114088 |
rs377712648 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018118 | TTTTTCCAAATGTCT[C/T]CATTGTAATGGAATA | 114088 |
rs377716398 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054688 | AAGCTATTCTCCTGC[C/T]TCAGCCTCCGGAGTA | 114088 |
rs377753535 | snp | G/T | 0.011925 | 0.0764466 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072108 | CCTGAAGCCCAGGTG[G/T]CCCAGTCCTGCCACG | 114088 |
rs386381356 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978764 | TTTTATCTGTTTTTT[-/TT]TGTTTTTTTTTTTCA | 114088 |
rs386381357 | in-del | -/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978773 | TTTTTTTGTTTTTTT[-/T]TTTTCACTGATGTAT | 114088 |
rs386472336 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062900 | TTTGGAAATTCCAAG[A/G]TATCTATAAAGTAAT | 114088 |
rs386777440 | in-del | C/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980993 | GTATTTTTTTTTTTT[C/TT]CAGAGACACTAATGA | 114088 |
rs386777441 | multinucleotide-polymorphism | AC/GT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982269 | GTCCTGGGAGTTGGT[AC/GT]TCTCTGCACCAGAAG | 114088 |
rs386777442 | in-del | -/GTG/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002123 | TGTGTGTGTGTGTGT[-/GTG/T]TTTTTCTTTTTTTTG | 114088 |
rs386777443 | in-del | AG/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014923 | AGGAAGGACACAAAC[AG/T]GGCCTAGGAGAACAG | 114088 |
rs386777444 | in-del | CTC/GTATTAGTAT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031908 | ATATACTAAACAAAT[CTC/GTATTAGTAT]ACCATTTGTATTGTG | 114088 |
rs397716299 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028258 | GTATTTGATAAAAAA[-/A]TTGCATTATAAGATA | 114088 |
rs397773997 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053173 | CAAAAAAAAAAAAAA[-/A]GAGAAGAAAACTTGT | 114088 |
rs397783519 | in-del | -/TT | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978765 | TTTATCTGTTTTTTT[-/TT]GTTTTTTTTTTTCAC | 114088 |
rs397792941 | in-del | -/A | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010140 | AAGCGAAAAAAAAAA[-/A]GAAAAAGAAAAAGAA | 114088 |
rs397796135 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059810 | TCAAAAAAAAAAAAA[-/A]CAAAAAAAACACAAA | 114088 |
rs397812830 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085431 | CTTCTATGCAAGGCT[-/T]ATGAAAAACAGTTTT | 114088 |
rs397827334 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028257 | GGTATTTGATAAAAA[-/A]ATTGCATTATAAGAT | 114088 |
rs397852023 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084182 | TCCACACTTTTTTTT[-/T]ATATATATTTAGTGA | 114088 |
rs397852468 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018003 | CATCATTCATGATGG[-/G]CTTGTAATCAATCAT | 114088 |
rs397852650 | in-del | -/TTAT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062111 | AAATAAATTATTTAT[-/TTAT]GATATTGTGCTTTTC | 114088 |
rs397852706 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054455 | TTTTTGTATTTTTTT[-/T]GTTAGAGATGGGGTG | 114088 |
rs397852806 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980994 | TATTTTTTTTTTTTT[-/T]CAGAGACACTAATGA | 114088 |
rs397853072 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992428 | ACGGAAAAAAAAAAA[-/A]GCCAGGTGTGGTGGC | 114088 |
rs397853121 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039766 | AAACTTTTTTTTTTT[-/T]GAGGCGGAGTCTCTC | 114088 |
rs397853204 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021999 | AAAAACACATTTTTT[-/T]GCCTGTGTATGGCCA | 114088 |
rs397853265 | in-del | -/GT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030598 | ATGGTGTGTGTGTGT[-/GT]ATGAGTGTGCATATG | 114088 |
rs397853537 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053173 | TCAAAAAAAAAAAAA[-/A]GAGAAGAAAACTTGT | 114088 |
rs397946283 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027847 | ATATCTTTTTTTTTT[-/T]CCTGAATGAGTAAAA | 114088 |
rs398025048 | in-del | -/A | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995783 | CAAAGAAAAAAAAAA[-/A]TCTCTAAAGCAAACC | 114088 |
rs398025049 | in-del | -/AA | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007816 | AAAAAAAAAAAAAAA[-/AA]GGACAAAATAAGAGA | 114088 |
rs398025050 | in-del | -/AC | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080479 | CACACACACACACAC[-/AC]GGAGAAACAACTAAA | 114088 |
rs398077757 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045065 | AAATATGGAAAAAAA[-/A]ATCAAATACTGCATA | 114088 |
rs527262883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018180 | TTGAGGTGGTTCTTG[A/G]CTTGAATTAGTTGCT | 114088 |
rs527319023 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029958 | CCAGAGAAGGTGAGA[A/G]GATGACTATGATTGA | 114088 |
rs527329651 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050131 | ATGGCCATAGGACAC[C/G]CTTCTTACAGAAGAC | 114088 |
rs527353023 | snp | A/G | 0.00716266 | 0.059414 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095114 | GCTCTGTGAGCCGCA[A/G]CCGCGTAGCCGCCGC | 114088 |
rs527382175 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982188 | GGGCGGGTGAGGAGC[A/G]TTGTGTAGCGTTTTC | 114088 |
rs527386518 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097567 | TGAGTTCTACTCTCT[G/T]CAAGCTCTGAATGTG | 114088 |
rs527389071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018663 | GCTACAATGGGCACA[C/T]GGAGGCCCTCAGTAA | 114088 |
rs527390768 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074544 | TTTCACCTTCCATCT[C/T]TCTCAATCAAATCTT | 114088 |
rs527428034 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063017 | AGAAAAATCAAGCAA[C/T]AGAAACACCCTGAGA | 114088 |
rs527476536 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083012 | TCTGTAAAATGAGAA[C/T]AGTAATGGTTCTTGC | 114088 |
rs527480366 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997604 | AGTCATACAAATCCA[C/T]GACTGGAAAGAACCT | 114088 |
rs527504063 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035461 | TTTCACTTTAATACA[C/T]ACATTTCTAATACCA | 114088 |
rs527524917 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082278 | AAGGTAATTGAAAAC[A/G]TGTCCACATAAAAAC | 114088 |
rs527525826 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052315 | TAAAAATAACAAAAG[A/G]GTCAAGGTCGGCGAA | 114088 |
rs527590892 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076207 | GACACACTCAAGAGG[A/G]AGAAGTTGAGATTTT | 114088 |
rs527616776 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990574 | TATTTGAAAAGGTAG[A/C]CTTTGGGGTGTTATT | 114088 |
rs527680391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084724 | AGTTTTATGAATTGA[C/T]GCACTTCATGATTGC | 114088 |
rs527689324 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037706 | CAGAGACTCTTTGGC[A/T]CTTTAAAAAAATTTT | 114088 |
rs527733719 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052843 | GAGCCCCATACCTCA[C/T]TGCTGCCACTGATGG | 114088 |
rs527754127 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071560 | ATCCCACCACTTTGG[A/G]AGGCCAAGGTGGTAG | 114088 |
rs527761559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985734 | TCACTTTCTAATGCC[A/G]TAATACATGGACCAC | 114088 |
rs527767304 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048700 | AAAACATCCCATCTC[A/G]GGGGCCGGGCGCAGT | 114088 |
rs527768410 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031895 | CAGCACATCTCTCAT[A/G]TACTAAACAAATCTC | 114088 |
rs527789889 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078340 | CAAATCCAATATTTA[C/T]ACAAATTTTATAGTA | 114088 |
rs527798168 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019951 | TTCAGAGAGGGACAT[A/G]AGTAGATTATAAAGA | 114088 |
rs527803014 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018313 | CCTTCCCTCCTCCCT[C/T]CCTTTTTTCTTTCCT | 114088 |
rs527822313 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071066 | GATGGGGACGACAAA[A/G]TAAGAATCCTGTCAC | 114088 |
rs527881994 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090956 | CAGGATTTAGGAATG[C/T]GAACTGCTTAAAATC | 114088 |
rs527922790 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071038 | CATTTACATTTCGGG[C/G]TTTTGGTGGACTGAT | 114088 |
rs527928239 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012031 | ACTCATTCATTCATT[A/G]TTTCTGATTTTTTTG | 114088 |
rs527956296 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057916 | AGATCAGTTAAAGAC[-/A]AATTTATTGAAAGGA | 114088 |
rs528013102 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050442 | GCCTTCCACCATGAT[A/T]GTGAGGCCTCCCCAG | 114088 |
rs528055637 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007049 | GACTCAGGAGGGCAA[C/T]GAATGGGGGAGGAGA | 114088 |
rs528097176 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051628 | ATTAATAAATCACCC[C/T]AAACTGAGATTGATA | 114088 |
rs528126385 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993436 | TGGAATGGTGCAATC[G/T]CAGCTCACCGCAACC | 114088 |
rs528132183 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006479 | AAGTTCTATTGTGTC[A/G]TGACCTTTGGCTTTT | 114088 |
rs528173584 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061274 | AAAAGTTAGCTGGGC[A/G]TGGTGGTGGGCACCT | 114088 |
rs528193280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039115 | ATGCAAAGATTGGCA[C/T]AGCTTCTTTAAAAAC | 114088 |
rs528208550 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046100 | GGCTTTGGAATGACC[A/G]CGTTTTAGAAATGGA | 114088 |
rs528209563 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040837 | ACCCTTAACTCTTCC[A/G]CTTACTACCACTGCT | 114088 |
rs528251503 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019464 | CCAAAGCTTTTTTGC[-/T]TTTTTTTTAGCTCAT | 114088 |
rs528262208 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020281 | GGAGAGGAGAGCGAG[C/T]GAGCCGTGGAGGCCT | 114088 |
rs528274743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978926 | GACTATGTTTTCTAC[C/T]CCTTAGGACCTAACA | 114088 |
rs528322844 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086415 | ACATTTTAGCAAAAA[C/G]TATAAAATACAGGCT | 114088 |
rs528364232 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000016 | CTTGGGAAGGTAGCA[A/G]TCTTCTGGTACCAGT | 114088 |
rs528398938 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020996 | GTTATGGCTAGGTAC[G/T]TAAATAGTTGTTCCA | 114088 |
rs528401425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998755 | GGGAAGGGGGAGGAA[A/G]CAGGGAAAGGAGGAA | 114088 |
rs528416400 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065117 | GTGGGCTGGTTTCCT[C/G]AGAGCTTTGTGTTAC | 114088 |
rs528502481 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079470 | GGATTCTGTGTTTAC[A/G]TATAGTTTAATCATT | 114088 |
rs528514600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027769 | TCTCATTTGGAAGAG[C/T]AGGCAATAATATGAG | 114088 |
rs528564710 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015762 | CCTCCAGCCTTGGCC[A/C]CCCAAAGCATTGGGA | 114088 |
rs528589918 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042817 | TCTGGTACAGACCTG[-/C]CTCCTGGCAGTTCCT | 114088 |
rs528652743 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986521 | CCTTCAGTTGTCCTG[A/G]GAGTTACTACCTATT | 114088 |
rs528729275 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029442 | ACTCCCGCTCCTTCC[C/G]AGGTACAAAGATAAA | 114088 |
rs528729664 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079367 | AATTCATAAATTATT[C/G]TTTACTTCCTGCCCT | 114088 |
rs528743464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980245 | AAATAATTATACTCT[A/G]AGATGTAGTGATTTT | 114088 |
rs528749013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066376 | TTTGTCTTTGTCTCA[C/T]ACAACTTCCCAGCAG | 114088 |
rs528784851 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987213 | CCAGAGGGTATTTCC[A/G]TGAATTTTTTTCTGG | 114088 |
rs528853972 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069620 | CATGGCATTGTTGGT[G/T]TTTTTAATTTAAAGC | 114088 |
rs528865585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013457 | GTTTGAAGTTAGGAA[A/G]TGTAAGAACTTCAAA | 114088 |
rs528904706 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057859 | GGAGGTAAGTGGAAA[A/T]GATGTCTACAGAGCC | 114088 |
rs528917770 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999887 | ACATGCCGGCAGGTG[A/G]TGGCACATGAATCAT | 114088 |
rs528928220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012858 | TGTTTGTGTACCCTC[A/G]CTGCTAATCAGGTCT | 114088 |
rs528943090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020068 | CTCCTCTCTTTGTCA[A/G]CAAAAAGCAGGCCCT | 114088 |
rs528972249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092851 | CAGGGATAAATACTA[C/T]TGAGGAAAATAAAGC | 114088 |
rs528988614 | in-del | -/TTTGTT | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057437 | TTGTATATAAAAGGA[-/TTTGTT]TTCTGGAAGTCACCA | 114088 |
rs529120934 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085513 | ATTCCTTTTTATATG[A/G]TGAAAGGTGGATCAG | 114088 |
rs529134397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030985 | AACCTTGTCTCTACT[C/G]AAAATACAAAAAGTT | 114088 |
rs529147985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057174 | CCCCACAATTCTTTG[C/G]TAGACATTGCTGCTC | 114088 |
rs529185843 | in-del | -/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097658 | TTACTTTTTTTTTCC[-/T]TTTTTTTTTTTTGAG | 114088 |
rs529194183 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019404 | ATTAACTATAATTTA[C/T]ATTTCAAACAGTTTC | 114088 |
rs529199728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071541 | ATGGTGGTTTACACC[A/T]GTAATCCCACCACTT | 114088 |
rs529219735 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021179 | GTGACAGTTTTTTAG[C/T]AATGTTAGGCCAGGT | 114088 |
rs529272861 | in-del | -/T | 0.00845933 | 0.0644834 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021993 | AATTCAAAAACACAT[-/T]TTTTTTGCCTGTGTA | 114088 |
rs529280212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026859 | GTGGGAAGAACAGTA[A/G]TACTTTGTAGTTGGG | 114088 |
rs529290163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073117 | GTTATCACAACACTG[C/T]GATACCACTGTACAC | 114088 |
rs529330625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059482 | ATGAAGAGAATGAAA[A/G]AACAAAACAAAACAA | 114088 |
rs529353529 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021739 | GCTGGACCCCTTCTG[C/G]TTTGCTCTTCCCATG | 114088 |
rs529354740 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038430 | CTGAGAAGGCAGTTG[A/G]TTAAGAGCTGGATGC | 114088 |
rs529375162 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085283 | GAGAATTAACCATCT[A/G]CATGTACTCCTGACA | 114088 |
rs529440506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000260 | TAATGAACGCTTGCT[A/G]TGTTCTAGGCAGCAT | 114088 |
rs529459134 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066294 | CTTTTCATCCCCGTT[A/G]CTTCACTGAACCACT | 114088 |
rs529487513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992877 | TGTAGTTTCAAGAAT[C/T]CCAACCTATTTGTCA | 114088 |
rs529531894 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986416 | ATTGGAAGGTTTCCT[C/T]TTAATTAAATAAAAT | 114088 |
rs529570288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079049 | GTAAAATAAAATAAA[A/G]TGCTCTTGATTAATT | 114088 |
rs529574492 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046250 | CACTTGTGGGGCTGG[A/C]CCTAGTTATTATCTT | 114088 |
rs529585086 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072520 | TTAAAAAGAGACTTA[C/T]CAATAAAAAACAAGT | 114088 |
rs529652642 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080828 | GTTGGGTAAGGAGGA[A/G]GAGGAACAGCTGCTA | 114088 |
rs529690309 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095325 | CTCGCGGCTGCAAGA[G/T]CTCTGAAGGGGGCCG | 114088 |
rs529713384 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995098 | CTCACAGGATCCTCC[C/T]GTCTCAACCTCCCAA | 114088 |
rs529769807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988778 | AATTCTCCCTTCATG[C/T]CCTTCCCCATGGGCA | 114088 |
rs529778058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034773 | AATAGCATGGATTCT[G/T]GCCCCAAACTACCTA | 114088 |
rs529804891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081472 | CATGGAGTTAGCATG[C/T]GACTCAACAATTCCA | 114088 |
rs529823533 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052409 | ATATCTGTAGGAATT[C/T]CTCTTCTCCTGGGAA | 114088 |
rs529834212 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008173 | GCTATGACTTTAAAG[G/T]GGTGGCAGGAGGGAG | 114088 |
rs529851324 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995686 | TGAAGTTTGAAAAGG[C/G]ATTAACTCTTGCTAA | 114088 |
rs529871486 | snp | A/G | 8.46633e-05 | 0.00650572 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094325 | CACCAGGCGGTGCTT[A/G]GCTAGGGGCCCCCGG | 114088 |
rs529924116 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060053 | AGTAGATTCCACCAA[A/C]CTGGGAGTCACAGAT | 114088 |
rs529934281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047520 | TATAAAGTTAGAAAC[C/T]AAGAGAGGACACTCT | 114088 |
rs529962772 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057345 | AATAATCCAAATTAC[C/T]AAATTACCAAAGTAA | 114088 |
rs530036224 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053022 | GACAACAGCCAGGTG[C/T]GGTGGTGGGCACCTG | 114088 |
rs530039858 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001011 | GTCAGACTGGCTCCT[G/T]ATTTGCTGTGAGGCC | 114088 |
rs530079825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010042 | TTAATGAATAAGGAC[C/T]GAATTCTTGGGCAAG | 114088 |
rs530094606 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996894 | AAGCACTGTTTTCAC[A/G]GCTAGGGGCCTTTCA | 114088 |
rs530117185 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051790 | TGGCCAACATAGTGA[A/G]ACCCCATCTCTACTA | 114088 |
rs530126161 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054547 | TGCCAAAGTGCTGAG[A/G]CTGCAGGAATGAGCC | 114088 |
rs530151891 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089285 | TTTGATTCTTAAACA[G/T]TTATCTTGTTATAGG | 114088 |
rs530158249 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029948 | GCATGTACAACCAGA[A/G]AAGGTGAGAGGATGA | 114088 |
rs530160507 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993445 | GCAATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC | 114088 |
rs530213288 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067936 | AAAGTCTTGTGTATT[A/G]TTGTATGCCAAATTC | 114088 |
rs530249868 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048851 | TAGCTGGGTGTGGTG[A/T]TGGACGTCTGTAGTC | 114088 |
rs530308150 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976338 | TGAAAGATCTTGCCC[A/G]TGAGTCTCTTTGACC | 114088 |
rs530326056 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981709 | GTTTGATTTCCTGAA[C/T]GTGGTCTATGTAATA | 114088 |
rs530349329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028642 | AAGGGAGAAAGGTAC[A/G]TTCTAAAGCTGTTTA | 114088 |
rs530370846 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060741 | CAAAGTGCTGGGATT[A/G]CAGGCGTGAGCCTCT | 114088 |
rs530391032 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086983 | TCTCTACAGTTATTT[A/G]ATAAAAAAGTGTCTG | 114088 |
rs530421122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016392 | TGCAAGGGATCTAGG[A/T]TGCCCGCTCCTTATG | 114088 |
rs530425013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023536 | TCACCCTGCCATAAA[A/T]ATCAGATATGACCCA | 114088 |
rs530428815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046771 | TTAAAAACTCTATAC[C/G]TTCGTTTCCTTCTTA | 114088 |
rs530471392 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063725 | TAAAACTCAGAATTT[C/T]ACATCCAAAGAAAAT | 114088 |
rs530485445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080772 | AAGAACCTTATGATA[C/T]TATACTGAGGTAGAC | 114088 |
rs530489003 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047461 | CTTAGAAAACCATTC[A/G]GTGCAATGAGGACAC | 114088 |
rs530498356 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999122 | GGTAGGGTCTCGATT[G/T]TGCATTTTTAACAAG | 114088 |
rs530525977 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095099 | CCCAGAGAGGCGCTA[A/G]CTCTGTGAGCCGCAG | 114088 |
rs530581543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995003 | CTCATATAATAATGC[A/G]TTCTCCTTTCCTTTT | 114088 |
rs530604620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040477 | TGACATAATTTTATT[C/T]ATGCCTACTTTGAGA | 114088 |
rs530653179 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022240 | GGCCCCTGCCTTCAT[C/G]AATGGACGAATGCTA | 114088 |
rs530703431 | in-del | -/A | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070779 | AGAAAAATGGCACAG[-/A]TGTATTTGTTTCTGA | 114088 |
rs530707869 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052422 | TTCCTCTTCTCCTGG[G/T]AATTAAATTTGATTA | 114088 |
rs530718874 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063009 | AAAAAGGAAGAAAAA[C/T]CAAGCAACAGAAACA | 114088 |
rs530745307 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051688 | AAAGATGGAATAGGC[C/T]GGGCGCAGTGGCTCA | 114088 |
rs530746028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066166 | TTTCACCATATCTCC[C/T]CCAGTTACTGCCCCA | 114088 |
rs530773121 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000451 | AATGCAGGCAGTCTG[A/G]CTCCAGTACTGCATG | 114088 |
rs530847751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093697 | CGACCCCACCGCCCC[C/T]ATCCCAGTCCCTCCC | 114088 |
rs530848897 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007183 | TTTTCCTCTTTCACC[A/G]AAAGCCTTTCTATTG | 114088 |
rs530853161 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993717 | ACAAGGTGTTTTCAG[C/T]CACCTTGCAGACAGA | 114088 |
rs530854116 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057719 | TAAAAATCAAAATCA[C/T]GGCCTTTTAATCTGA | 114088 |
rs530873971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010811 | TGCACTTTTCTGTGA[A/G]GCTGACTCTGCTGAG | 114088 |
rs530914248 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059433 | TGTATTTGTTCACCA[A/G]TTTTCAAATTGGAAG | 114088 |
rs530920994 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095671 | CCTTCTCCGTGAATC[C/T]GCTGACGCCGTGCCC | 114088 |
rs530922058 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016337 | ATCAGCAGCGGCATT[A/G]GATTCTCACAGGAGC | 114088 |
rs530935656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009841 | AAAGGTTCCTTATCA[C/T]TGGGATCAAAGCTTA | 114088 |
rs530981624 | snp | C/T | 1.64933e-05 | 0.00287165 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022814 | GTTGGCTTTCTGCTC[C/T]TCCCATGATGCAGCA | 114088 |
rs531019846 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054481 | GGGTGTCATTATGTT[G/T]CCTAGGCTAGTCTGG | 114088 |
rs531019926 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048395 | CATGGTATCAGGATG[C/T]TGAGTAAGTGTTTCT | 114088 |
rs531097046 | in-del | -/A | 0.158632 | 0.232706 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974999 | AGTGAGATTCCGTCT[-/A]AAAAAAAAAAAAAAA | 114088 |
rs531099469 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027909 | TTTTATTATAACCTA[C/T]GTTTAGTAACCACAC | 114088 |
rs531120216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022448 | AACCATGAGCTAAAT[A/G]TAATTCTATTATTTA | 114088 |
rs531120427 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061839 | AAGTAACTCTTCATC[C/T]TTGGAAAATTCCAAG | 114088 |
rs531126813 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032683 | CAGAGTCTGTGTCCA[C/G]GGAACCCAGTCTAAA | 114088 |
rs531139963 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981031 | ATCCTGGGGAAATCT[C/T]GGAGCATAAGGTGGA | 114088 |
rs531147491 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074870 | GCATAGGTAAAATGA[A/G]GGGAATGAAAGATGC | 114088 |
rs531169547 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033980 | TATCTGTCCACAAAA[G/T]AAGTATAAATGCTAA | 114088 |
rs531178052 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023939 | CAAAGTCATAAAGAA[A/C]TGTGTCTTTTTATAT | 114088 |
rs531179881 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029433 | CCAAAGCCCACTCCC[A/G]CTCCTTCCCAGGTAC | 114088 |
rs531187676 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067820 | ACATTCTACCATTTA[C/T]TTTTCCTCACAGCAC | 114088 |
rs531215975 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990428 | TGGCAGGAGACTCAA[C/T]CATAAGAAAAATAAT | 114088 |
rs531239796 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029131 | TTCCCACTGTAAACA[G/T]TCTTCACGTGGCCTT | 114088 |
rs531241415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028534 | ATTCAGGACCACAGA[A/G]CAGTGCTGGAAATTT | 114088 |
rs531249027 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035841 | AGGCATATTTTTGAA[C/T]CTCAGTTGTAAATAC | 114088 |
rs531260587 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042715 | ATCCCTCTAAGGTCA[-/C]TGGAGGCTTAGTCTT | 114088 |
rs531319051 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076141 | GGTGGTGTGTTGCCT[A/G]TTTCACAGATGAGGA | 114088 |
rs531334566 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014923 | AGGAAGGACACAAAC[-/A]GGGCCTAGGAGAACA | 114088 |
rs531398233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002947 | GGATGAAATCTTATC[A/G]AAGAGCTACAGCTAC | 114088 |
rs531415087 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977054 | TTGGTGGGCTGTCTA[A/G]GTCCTTTGTTGGTTA | 114088 |
rs531432256 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088651 | TTTCGAGTTGGTAAA[A/G]AAAAAAAAAAATCTC | 114088 |
rs531433238 | in-del | -/TTT | 0.312348 | 0.242101 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053510 | TCAGAACAGGTATTC[-/TTT]TTTTTTTTTTTTTTT | 114088 |
rs531436893 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092117 | AACATGGACTATAAT[A/T]AGCAGTTTAAAAGTG | 114088 |
rs531445907 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094014 | AAGGCACCTGCATTG[C/T]GCCCCCACTGGGATG | 114088 |
rs531477882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982793 | CAGATAGAATGATGT[C/T]TTTGTACGCATTGTT | 114088 |
rs531484799 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073762 | GGAAATTCATTGAAA[G/T]GTACATTCATGATTT | 114088 |
rs531500212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042471 | ACCAAAGATTTCCCT[C/T]TTAAATCTTTTATTT | 114088 |
rs531522600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089159 | CTCCTTGTGAGTTGA[C/T]TTTATTTCACTTCCC | 114088 |
rs531559117 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096386 | AAGTGACATTCTGAG[A/G]TAGTAACATTTGAAA | 114088 |
rs531564169 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044474 | AAAGTCCTTTAAAGG[G/T]AACTGATTCAGATGG | 114088 |
rs531603179 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989896 | GATAAGGGCAGAGAC[A/C]TCTGCTTAAAAAAAG | 114088 |
rs531650812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082222 | TGAGCCAGGAACCAC[A/G]GACAAAGACCAAATA | 114088 |
rs531689817 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089748 | AGAGTCTCACTCTTT[C/T]AGGCCACCTTTCAGA | 114088 |
rs531699304 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036736 | CAGAACCCATGCATA[C/G]AGAGGGCTGACTGTA | 114088 |
rs531726290 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069147 | GGAATCAGTCTGAGA[C/G]AGTTGGGCCTTCTTC | 114088 |
rs531793082 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016460 | CATCCCAGAACCATT[A/C]CCCCCCACCCCCTAC | 114088 |
rs531803696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055190 | TTATTTCATTAAATC[C/T]AAAAGCCATCAACTG | 114088 |
rs531826974 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062857 | TGCCAAGTGAAGAGG[A/G]GTTAGAGCTTGAGTC | 114088 |
rs531856098 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046774 | AAAACTCTATACCTT[C/T]GTTTCCTTCTTAGTA | 114088 |
rs531874303 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999176 | TGGGGGAGGACCGCA[A/C]TTTTGAGTAGAGGAA | 114088 |
rs531876651 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049846 | AAAAATAAAATAAAA[A/T]AAAAATAAAAAGATT | 114088 |
rs531895080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015426 | CCCCACCTCCATTTA[C/T]CTCTCCATTTTACAT | 114088 |
rs531920827 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011372 | ATATATTTTTTTATT[G/T]CCAAAGATGGGGTCC | 114088 |
rs531936946 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011910 | GTTTTCATGTTGCCA[A/C]AACCAATGGTTACAA | 114088 |
rs531955139 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079148 | CAAAAGCCTTCATAA[-/T]ATGCAAATTAAATAA | 114088 |
rs531963544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028712 | GTTTTCTAGGTTACT[G/T]AAAAGGTGTCACGAT | 114088 |
rs532051863 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047644 | GTAGGATAAGGCAAC[A/G]TACCCAAGGGAGGTA | 114088 |
rs532097185 | snp | C/G | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022928 | ATCACATTGGGCCAC[C/G]AGACAGGCTTCAAAC | 114088 |
rs532149944 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067987 | GCAGGCATTCAATTG[A/G]CACTTGCTGAATACA | 114088 |
rs532189460 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068571 | TTTATCCCCGTTTTA[C/T]AGATGACAAAAATGG | 114088 |
rs532209599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982213 | GTTTTCATGCTGCCA[C/T]GCAGGAAGGAGGCGT | 114088 |
rs532209787 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047655 | CAACATACCCAAGGG[A/T]GGTATGGTCTAGTAC | 114088 |
rs532210960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081104 | CTATGTCTCTTCCAT[C/T]TTAAAAGTGAATAAG | 114088 |
rs532223298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029085 | CAAGCTGCTGAGTGT[A/G]CCCAGGCAGAAGACA | 114088 |
rs532242719 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095298 | TAGAGTCTGAGGATA[A/G]GGCAGTCTTCGCTCG | 114088 |
rs532262707 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001493 | CTCTGCCTCCCAAAG[C/T]GCTGGGATTACAGGC | 114088 |
rs532273300 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989754 | GGACGGGACTGTGTT[A/C/T]GTAACGAATACGTAT | 114088 |
rs532274569 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075424 | TGGAATCTAGGTAAT[C/G]TGGATTTGCAACATG | 114088 |
rs532278534 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996578 | GGCATGCACTTCACT[C/T]TTCAATCAAACCACC | 114088 |
rs532298477 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038370 | TTGTTTTAAGTTGCT[A/C]AGTTTTTTGTACTGT | 114088 |
rs532323935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030355 | ATGGATCCCTTCTCC[A/G]GTTTCTCTGGTGCTG | 114088 |
rs532331098 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095618 | TTCGCAGGCGTCTCA[C/G]CCGGGCCTAGGCTTC | 114088 |
rs532336277 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076120 | TCCTGCTCTATAACT[A/G]TAGGAGGTGGTGTGT | 114088 |
rs532344350 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087515 | GTTTAGGGTTGTGAG[A/T]ACACCCCAGGGGAAT | 114088 |
rs532358612 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053757 | CCCCGCTCCCCCGAC[C/G]CCACCACAGTCCCCA | 114088 |
rs532369143 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090074 | CCTGGATCTCCTGTT[A/G]TCTAGTTCTTTCCAT | 114088 |
rs532387709 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995896 | CTGATTTCTAAAAAA[A/C]AAACAAAAAAGAGAT | 114088 |
rs532423252 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990620 | GGAAAAGCAAACAGA[C/T]TGTGGTTGCTTATGA | 114088 |
rs532438271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017865 | GCTGTGTATGGGGCT[C/T]CCTCGTGATTCCATG | 114088 |
rs532443062 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003181 | GGACTTTCCTTTTTA[G/T]TTTAAATTTGTTTTC | 114088 |
rs532457863 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033153 | GGAGTGCAGTGGTAC[A/G]ATCTCAGCTCACTGC | 114088 |
rs532471782 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083080 | GAAATTACTTAGATC[A/T]GTGCCTAGACCACTA | 114088 |
rs532520253 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005063 | AAGTTTAGACTTTAG[C/G]AGAACTACAAGCTGT | 114088 |
rs532590501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011325 | ATTTGTCATTTGTGT[C/T]CTCTGCTCAGTAACC | 114088 |
rs532628522 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036044 | ACTCTAGGTAAAAGC[C/G]ACAGAGACTTGGCAA | 114088 |
rs532656794 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997723 | GGGAGCCTGCTCTAG[A/C]GCCTAGATACATTTG | 114088 |
rs532683149 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048876 | GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG | 114088 |
rs532685534 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988179 | CAATTCATGATATTG[A/G]AAATATTTGTTGCTT | 114088 |
rs532696011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062199 | TCAACTGTTTATGCA[A/T]GTTATTCAACTTTTC | 114088 |
rs532741163 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091925 | CATTTCAAATTGACA[A/T]GGGGCTTGACAGAGA | 114088 |
rs532750924 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012160 | TATTGTGCAACTATC[A/T]CCACCATCCATCTCC | 114088 |
rs532799714 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977996 | ATCTAGTATAATATT[A/C]TTTGAAAGGGAAATG | 114088 |
rs532855824 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018015 | TGGGCTTGTAATCAA[C/T]CATAATTGTGGTTAA | 114088 |
rs532976479 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056122 | AAAAGCAAACGTCTA[C/G]AATGGTACAAAAATT | 114088 |
rs533022658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984337 | AAAAGAATTTTACAA[A/G]AATTAAAAAAGCAAC | 114088 |
rs533032392 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070911 | TTTCTTTCTTTCTTT[C/T]TTTGGTGGAGATGGG | 114088 |
rs533033495 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050539 | TTATCAGCAGCATGG[G/T]AACAGACTAATACAA | 114088 |
rs533086975 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039719 | CTGCAAACCTCAGAT[C/T]TGTATATTTTATTAT | 114088 |
rs533090223 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057101 | TCAGACATTATATCT[A/G]CATGGCCACAGATGC | 114088 |
rs533128119 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077023 | ATTTTAGCGCTTGCT[A/G]TAAAAGGGCTTAACA | 114088 |
rs533139244 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088648 | TAATTTCGAGTTGGT[-/A]AAAAAAAAAAAAAAT | 114088 |
rs533193176 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031992 | TTTTATTCCAACACA[A/C]TGTTACATAGAATCC | 114088 |
rs533200350 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036609 | TAAATAATTGTTACA[C/T]TATACTATTTATGGA | 114088 |
rs533210919 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032852 | TACAGGTTGAATATC[C/T]CTGTTCTGAAAATCC | 114088 |
rs533212788 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063169 | GAAAGCTATAAAAAA[A/G]GCATCAAATGGAGAT | 114088 |
rs533220812 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065392 | GTCCAGAAAACCCTC[A/C]TTGATGGATAATGGA | 114088 |
rs533262659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026819 | TGAGAAAGTTACCTT[C/T]GTCTGAATTACTCCA | 114088 |
rs533304287 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072343 | CATCCAACGAGAATT[C/T]CTAAACCTCTGAAAT | 114088 |
rs533314962 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037858 | CTTGGGAGGGTAAAA[A/G]CCGTTCTTGTTACAT | 114088 |
rs533326820 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045167 | AGCTGGTGAGCTGGC[A/G]TCTGTGATGAGAAAT | 114088 |
rs533333905 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071732 | GATTGCTTGAGAGTG[G/T]GAGGTCAAGGCTGCA | 114088 |
rs533341748 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078939 | GTGAGATGATAGACA[G/T]GTTAGTCTGCTTTAC | 114088 |
rs533355491 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993184 | GCCAAGAGTATCCAC[G/T]GGTACCAGTGGGGGA | 114088 |
rs533436356 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038422 | TAACACACCTGAGAA[A/G]GCAGTTGGTTAAGAG | 114088 |
rs533444295 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060562 | AGCTCCACTTCCAGG[A/G]TTCACACCATTCTCC | 114088 |
rs533459628 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010305 | GCCCACCCAGGGCTG[C/T]TGGAAGTCTGACTTA | 114088 |
rs533482971 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083148 | CTTTGATAGACTAGA[A/G]CTCGATACTTTTCTC | 114088 |
rs533505122 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064501 | AAATATAAAGAATCA[A/G]AAGTTAAAAGGGGAA | 114088 |
rs533657400 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050341 | AGTGAGTAAGTCTCA[C/T]GAGATCTGATGGTTT | 114088 |
rs533657601 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063810 | ACAATTTGTTTCCAG[A/G]AGATTTATACTACAG | 114088 |
rs533698187 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055376 | GGCACCCCAAACATC[A/G]TGTCCACATCCTAAT | 114088 |
rs533698801 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074248 | ACATAGCAAGACTCC[A/G]TCTCTACAAAAAAAA | 114088 |
rs533808625 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976686 | CTACCCTGATGTGAA[A/C]CTGTGTAGCGGATAT | 114088 |
rs533817749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070595 | AATCTGAACTCTGAA[A/C]TGCTTCAATGAGCAT | 114088 |
rs533828688 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024017 | TTCGTATAAGGAATG[C/T]ATTAGTAATTGCTTG | 114088 |
rs533828784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016841 | AGAGACTTTTGTTTC[C/T]GAATATTTTCAATCC | 114088 |
rs533843771 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071819 | CAAAAAATAAATAAA[C/T]GAATAATTTTTAAAA | 114088 |
rs533879149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982415 | CTGGTGACTGGCAGA[A/G]CAGTGCACCAGAGAC | 114088 |
rs533894336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025575 | AACACTTCTGGCCAC[A/G]GCAGTCAAAGGCCCT | 114088 |
rs533904227 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051204 | CAGATAACTATAGGA[-/T]AACCTTCGTTGTTCC | 114088 |
rs533967325 | in-del | -/TTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053527 | TTTTTTTTTTTTTTT[-/TTT]ATGCGTTAACATTAC | 114088 |
rs533978459 | snp | C/T | 4.96899e-05 | 0.00498422 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982075 | GATGTCCGAGTGCGC[C/T]GAGCCAGGGTCGAAA | 114088 |
rs534068318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063266 | GCGGAATAAAAAATT[C/T]GGAAGGCATCAATAA | 114088 |
rs534073324 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987669 | TTAAGGGGAAATTAG[A/C]CTTTGAGTGTAATAG | 114088 |
rs534142260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093344 | GAGAAGTGGGTGTGT[A/G]TATAGTTGGGAGGAG | 114088 |
rs534188982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069886 | TTATTTGTGTATTCT[A/G]TATTTGCAAATTTGC | 114088 |
rs534252994 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056428 | AAACAAAACAAAATA[A/G]GCAAATTTATCATGA | 114088 |
rs534258393 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036256 | TAAAATCAACTATGT[A/G]TTTACACCATAGAAA | 114088 |
rs534263563 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994519 | ACTTTGTCCTACAAA[C/G]TCAGATGTCTAGCCC | 114088 |
rs534296435 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992358 | CAAGGCATGAGGATC[A/G]CTTGAGGCCGGGAGT | 114088 |
rs534354679 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068494 | CTGTGTGCCTGCAAC[A/G]TGCCAAGTACTTTAT | 114088 |
rs534359296 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999417 | ACATGAAATGGAACC[G/T]GAGGCCCTTATCTTG | 114088 |
rs534366350 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997920 | AGGAACAGCGGCTCT[A/G]TGCAGAATGCAGAGC | 114088 |
rs534378650 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018805 | AGCTAGAATTTTTCC[C/T]CAGAATCATTTGGAA | 114088 |
rs534426798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985478 | GTGTTTTTACTTTTA[C/T]TGTACTTTGTCAATA | 114088 |
rs534511178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990769 | TGTATTTTGGAGCAC[A/G]GTAAGGCAAGACATG | 114088 |
rs534512780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076719 | CTTTCATCTTCGCAA[C/G]AGTCCTTGGTGAATG | 114088 |
rs534533586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057370 | AAGTAATTTACAGAT[A/C]TTTCCTTAATTTTCT | 114088 |
rs534549896 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030526 | AGAGTAGCTGGGCCT[A/G]GGAATGGAAGCACAC | 114088 |
rs534581581 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089047 | AAGAAATTAGATGCC[A/G]TTATAATTCACTGAG | 114088 |
rs534586659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999992 | TCAATGGGGATAGGG[C/T]TCCCTCACCTTGGGA | 114088 |
rs534625274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038041 | AAATAATGGTCCTCT[A/G]AAATGTCCATGCCCG | 114088 |
rs534625321 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092141 | AAAAGTGAAATCAAA[A/T]TATGAATAAAAAACT | 114088 |
rs534722363 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051863 | TCCCAGCTACTAAGG[A/G]GGCTGAGGTGAGATA | 114088 |
rs534744838 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038524 | CATCTCCTGGTCTCC[G/T]TTTAAGTTGGAGAGA | 114088 |
rs534773547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012933 | AGTTCTTTATATATT[C/T]TGGATATCAGTCTCT | 114088 |
rs534833381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050308 | TGGGGGCAGTTTTCC[C/T]CATACTGTTCTCGTG | 114088 |
rs534839340 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019512 | TTTATACAATGATCA[A/G]TTATGAACTCATGCC | 114088 |
rs534883945 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075303 | CACGTTAATGTTCTG[A/C]AATTGGGATGTACTT | 114088 |
rs534909383 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058056 | TATAAACAGATTATA[G/T]TAATCTGACAGCCTA | 114088 |
rs534918532 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077753 | CTGGTGGAAAAGACA[C/T]GGATATGAAATCACA | 114088 |
rs534973980 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021271 | CACATGTGCTAATCA[C/T]CCACTTCTTCCCTGA | 114088 |
rs535015420 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034588 | ATTTGAAAGTTTAAC[A/G]CAGTTTCACCTCGGG | 114088 |
rs535050349 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025063 | TCAGGCTGTGTTTCC[A/G]GCTTGTTGGCAAAAA | 114088 |
rs535060977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092066 | CTGACAGAGTGATTA[A/G]TTTTTTAGTTCCAAG | 114088 |
rs535067608 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998859 | TCTTCAGCTGTACAC[A/G]TTGCAAAATTATGCT | 114088 |
rs535069509 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005750 | CAAATGCCACTTCCA[G/T]TTTTCTGGAAAGAGG | 114088 |
rs535108803 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046979 | ATGTATAGTAAGACT[A/G]TAAAGAAATGCATAG | 114088 |
rs535120989 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979057 | GTTAAGTCATTCTAT[C/T]TGTTTTCATGCCAGT | 114088 |
rs535138693 | in-del | -/TTCTAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086028 | GCACCACAATTTCTT[-/TTCTAA]TTCTAAATTTATTTT | 114088 |
rs535171697 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026917 | AATGTGAAAGCTTCT[A/G]CTAGTTAAGGGAACA | 114088 |
rs535172088 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065954 | TGATTTTTCTGAGCC[A/G]TTAGTCCCAGCATCA | 114088 |
rs535177093 | in-del | -/A | 0.0829038 | 0.185954 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080537 | TTAATGTAAATAATA[-/A]AAAAAAAGGGGTCTT | 114088 |
rs535193750 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037872 | AGCCGTTCTTGTTAC[A/G]TGTACACCATTAAGC | 114088 |
rs535273454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977555 | GGGCTCTCAAATCCT[A/G]GTGACATTTGATTAT | 114088 |
rs535279671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063240 | ATGGGCTTAACAATA[C/T]ACTGGAGTAGGCGGA | 114088 |
rs535361700 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030658 | GTGGGTAAGAATGTG[A/C]GTTTAAGAGTGTGTA | 114088 |
rs535383242 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058364 | CTACTCTAACGACAT[C/T]CTTGGTTGGGAAGCC | 114088 |
rs535394360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012259 | CCAGCCCCTGGCAAC[C/T]GCCATTCTACTTCCT | 114088 |
rs535396389 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048759 | GAAGGCCGAGGCAGG[C/T]GGATCACGAGGTCAG | 114088 |
rs535464647 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044374 | CAAGCAGCAATGTAC[C/G]TGGCTAAAAATAATT | 114088 |
rs535476459 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091223 | AATCTGGCCAGTTGA[A/C]AACTAGTGAATTTCA | 114088 |
rs535512771 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051784 | CCAGCCTGGCCAACA[C/G/T]AGTGAAACCCCATCT | 114088 |
rs535518534 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045590 | ACAATGTAGCATAAA[A/T]CCACATTGGTAAAGA | 114088 |
rs535578458 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044736 | AAATCATGAGTTTAA[C/G]CCAACCTTGTTTTGT | 114088 |
rs535581095 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006677 | AAAATGAAAATGGAA[A/G]ACTATAATCCAGTAT | 114088 |
rs535602269 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051259 | TTTGCAAGAAAGGAA[A/G]AGAACAGTGAGAGAG | 114088 |
rs535610314 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011618 | ATAATAGCCAAAAGA[G/T]AATCTAATAATAATT | 114088 |
rs535620400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055568 | GATGAATGGTTAGAG[A/G]GAAACAAGTTTGCTG | 114088 |
rs535673558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018380 | CCTTTCTTTCTTTCT[C/T]TCCTCTCTCTCATCT | 114088 |
rs535678302 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025426 | ACAAGGCCAGCGAGA[C/T]TCAAAACTGAAGAGT | 114088 |
rs535727634 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001566 | AAAACTTATTCTGAG[A/G]TTGAAACCCAAGTTA | 114088 |
rs535727642 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976964 | AACCTGATCAGAAAA[C/G]AAAGAAAATATAACT | 114088 |
rs535753051 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065488 | TCTAGCTACATGGAA[C/G]ACAAAGTCAAGGTTC | 114088 |
rs535766100 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086074 | AGGAGAAAAATGACT[C/G]AATTTCTCAGTAATT | 114088 |
rs535839202 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073600 | ATAGGCAAAGTTACC[A/G]TGCTGCTAGAAGGTT | 114088 |
rs535870264 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979865 | TGCTGAGAGTGAACT[A/C/G]ATTCATTAGGGTCTC | 114088 |
rs535912733 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067369 | GGACCACGACAACAG[C/G]CTACTAACTTCTACT | 114088 |
rs535938136 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059741 | AGGCAGAGGTTGCAG[C/T]GAGCCAAGATCGTGC | 114088 |
rs535953158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014329 | GCCGGGGAGTTTCAG[C/T]AGGGGTTTGCAATTG | 114088 |
rs535980251 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995099 | TCACAGGATCCTCCC[A/G]TCTCAACCTCCCAAG | 114088 |
rs536093089 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020661 | AAGCCATTCCTGGGC[A/G]ATGACATCTGCAGCC | 114088 |
rs536118543 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986770 | AGCCTTACCTTTGTT[C/T]CTGAATTATGATCAG | 114088 |
rs536119528 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992119 | TGGAAAGGCACACAC[A/G]TCACTGTCCTCCTTG | 114088 |
rs536130066 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046379 | TGGGAATAAAATCAG[-/T]GTACTTTATCACTGT | 114088 |
rs536137950 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040159 | AACTGTGCAAGAAAA[A/G]GTAAATATTTCCTCG | 114088 |
rs536152878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063973 | AGATTGTATAGTTTC[C/T]CTCCTTAATTTATCT | 114088 |
rs536153218 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032908 | TTTCCTTTGAGCGTC[C/T]TGTCAGCACTCAGAA | 114088 |
rs536164112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071953 | GCTACGCATTTGCCA[A/G]TCCCGGACTCAGCAG | 114088 |
rs536174067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079309 | CCAAATTGAGTAATA[A/G]TCTCTGACCTACTAA | 114088 |
rs536207282 | in-del | -/T | 0.0372436 | 0.131281 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084174 | AAACTTTTCCACACT[-/T]TTTTTTTTATATATA | 114088 |
rs536207778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027433 | ACAGGTGTGAGCCAC[A/C]GTGCCCAACCAGCTG | 114088 |
rs536223077 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995337 | CTCTAAGGCTTGTTT[C/G]CTTTTCTAGCTTGTA | 114088 |
rs536229593 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002385 | ATGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 114088 |
rs536279194 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087812 | CATCAAAAGTATCTT[G/T]AAAACAATCTATTTT | 114088 |
rs536285474 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002018 | TGCAAATTAGTTGAG[C/T]CTTCAGACACACATA | 114088 |
rs536297594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989179 | ATTCCAAATCCTTTA[C/T]TCTCCTGGTCATGCC | 114088 |
rs536327639 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052904 | GCTCATGCCTATAAT[C/T]CCAACATTTTGGGAG | 114088 |
rs536344012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022069 | ATCCTCTTTTCCTAC[C/T]TTTAGAATTTTTCTT | 114088 |
rs536360967 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996199 | TATATTTGTACACAA[A/T]ATATAAAATTCATGG | 114088 |
rs536361362 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988622 | CTATGACCTCCCATT[A/T]CCTACCAGCTGGGCT | 114088 |
rs536381309 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034454 | AAAAACAAAATACAA[A/T]TGAAAATATTTAGAG | 114088 |
rs536430439 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052707 | GCAGACCTCATTACT[G/T]ACACAGATTCCTTTT | 114088 |
rs536492883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093782 | GCGCGGCTCTACCCA[A/G]CTATGCAGTGCTTTC | 114088 |
rs536505317 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092891 | ACTAGCGGGTGTCTG[C/G]GTGGGTGGCGCTGCA | 114088 |
rs536510934 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994334 | ATTCCTTGAGCCCAG[A/G]TGTAGGAGGCTGCAG | 114088 |
rs536567023 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095339 | ATCTCTGAAGGGGGC[A/C]GGCGTGCGGAGGCTA | 114088 |
rs536573782 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993587 | TGGTCAGGCTGGTCT[C/T]GAACTCTTGACCTCA | 114088 |
rs536596994 | in-del | -/A | 0.428333 | 0.175206 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061415 | AGACTCTGTCTCAAG[-/A]AAAAAAAAAAAAAAA | 114088 |
rs536601493 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004566 | ACCTCAACAGGGAAC[A/G]CTAATCATAAGGGAT | 114088 |
rs536644380 | snp | A/T | 0.000123541 | 0.00785844 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986024 | GATCGGAAATCAAAG[A/T]AGGATCTCCCGGGGA | 114088 |
rs536649923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079268 | TCCACTCAGAAGAGA[A/G]TAATTGGCCAATCTT | 114088 |
rs536667891 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040854 | TTACTACCACTGCTT[C/T]AATTATTCTGAAAAT | 114088 |
rs536684031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078742 | ATAGTGGTTACCATG[A/G]TGGGGAGAAAATGAA | 114088 |
rs536717219 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979682 | CCGTTTCCCTAATCA[A/T]CCCTTGCACATAAAT | 114088 |
rs536717716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071554 | CCTGTAATCCCACCA[C/T]TTTGGGAGGCCAAGG | 114088 |
rs536718246 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075066 | TCAGTAAGTCTAGAT[A/C]CCAATTAAATTTGCC | 114088 |
rs536721454 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065850 | GGCCCACTTGAAGAG[G/T]GTGCTTTGACATTTA | 114088 |
rs536722434 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983592 | AAAAACTGCCCCTCT[G/T]CTCTTTCAAAATGAA | 114088 |
rs536743371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093730 | AGGGTTCGCAGCCCG[C/T]CCTGCCCTCGAGCGT | 114088 |
rs536780385 | snp | A/G | 2.06473e-05 | 0.00321298 | intron-variant, stop-gained | TRIM9 | GRCh38.p7 | 14:50979308 | AGCTTCCCTCTCTTC[A/G]GTTGGATTGAACGGC | 114088 |
rs536835740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060300 | TTCCTATGACCATTT[A/G]GCTAACCCTTTACTC | 114088 |
rs536878512 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091075 | TGAATAAAGGAATAT[A/T]GTTAAGTACTGGCAC | 114088 |
rs536888465 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022530 | CACTTATCTTGTTTA[C/T]TATTTGTCCCTCTTG | 114088 |
rs536907593 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993016 | AGGCAGGGCTGGAAA[A/G]CTTCTGTGAATAAAT | 114088 |
rs536967342 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000035 | TCTGGTACCAGTTCT[A/G]TCTGGTGAAAGGCCC | 114088 |
rs537003694 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026766 | ATATAGGTTTGAAAG[C/G]GTGCAGATTCTCGCT | 114088 |
rs537014888 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060618 | ACTACAGGCGCCTGC[C/T]ACCACGCCCGGCTAA | 114088 |
rs537045828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993509 | AAGTAGCTGGGATTA[C/G]AGGCGCCCGCCACCA | 114088 |
rs537048982 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032274 | ACTTGAGTTTCAGTG[A/G]TGGCATTTCACTAGT | 114088 |
rs537054037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039234 | ATGTTGCTACTGAGA[A/G]TGTTAAAATGGTAAA | 114088 |
rs537074310 | in-del | -/TG | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978485 | TCATGCCTTAGAAAC[-/TG]TGCACAGGCTGTTCC | 114088 |
rs537089785 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028650 | AAGGTACGTTCTAAA[A/G]CTGTTTATAATGCCT | 114088 |
rs537158654 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096743 | TTAAGCTGGCTTTCA[A/G]CTAGTTGAGACCAGA | 114088 |
rs537168385 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994483 | AGCCACAAAGTCTAT[A/C]TAAATAGACTAAATA | 114088 |
rs537178543 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040278 | TTGACTGAATTTTCT[C/T]TAATATTTGATGCTG | 114088 |
rs537232938 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999602 | CATTCAGGAAAAGGG[G/T]GCCTTGAGAGGCTTT | 114088 |
rs537266084 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044900 | TTGTTTTGTTTTTTT[C/T]TTTTAAGAAAGAACA | 114088 |
rs537279789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021321 | AGGTAGGAATGTAAA[C/T]GGTCATTAACACACA | 114088 |
rs537281139 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976666 | ATAGAGCCATCCTAA[C/T]GATCCTACCCTGATG | 114088 |
rs537286252 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058304 | TAGTTACTCAGGTGA[G/T]GTGAGGCTCACATCT | 114088 |
rs537290722 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013659 | TGTGAGTTTTGGGGG[G/T]ATCAAATTTAAAATT | 114088 |
rs537291461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092367 | CGGGTTAAGGAGTTG[A/G]GAAAACTTTCACTGA | 114088 |
rs537315968 | in-del | -/AAC | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025137 | TGTTTGTATGTAAAG[-/AAC]AACAACAACCACAAA | 114088 |
rs537342708 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062760 | AATCCCTGAACTGTG[A/G]ATGCATGGGAGAGAC | 114088 |
rs537354477 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007875 | GATGTACACATACCA[A/C]GTACAGGAACGCATT | 114088 |
rs537360299 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039631 | GTCATGAGGGGATTC[G/T]CTAAGGTATGGAATG | 114088 |
rs537405242 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095334 | GCAAGATCTCTGAAG[C/G]GGGCCGGCGTGCGGA | 114088 |
rs537482813 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023061 | AATGAAAAGGAACTC[C/T]GTCCACAATGCACAT | 114088 |
rs537507095 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048631 | GTGTGTCTAGGGTGT[C/G]GTGTAATCAATGAAA | 114088 |
rs537564510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080565 | CTTGGCAATATGTAC[C/T]GTGTCACTTGGGTGA | 114088 |
rs537591268 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061462 | TTTATTGTAAGGATA[A/T]ACATATTGAATTTAA | 114088 |
rs537609962 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034968 | ATAGTAAGTGTAATC[G/T]GAGTATTATGTAGCT | 114088 |
rs537624701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022025 | GGCCACCCTATCCAA[A/G]ATTTCCACCCCTATC | 114088 |
rs537628793 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066639 | CTGGCTTTTAGTCAC[G/T]ATTCTGGAATTGAAC | 114088 |
rs537676352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027392 | CAGGTGATCCACCCA[C/T]CTCGACCTCCCAAAG | 114088 |
rs537690883 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027806 | ATTTTAAAGAAGAAA[-/T]TTTTTTTCATTGTTA | 114088 |
rs537700945 | snp | C/T | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974889 | TGCCTGTAGTCCCAG[C/T]TACCCGGGAGGCTGA | 114088 |
rs537724578 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060543 | ACGATCTCGGCTGAC[G/T]GCAAGCTCCACTTCC | 114088 |
rs537783289 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989029 | CTCCACTCTCCAATT[A/G]TAGCGTTACTATCTG | 114088 |
rs537833545 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061067 | TCATGTCCTTAATGG[C/T]ATTCCTACATTTTTT | 114088 |
rs537845442 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975777 | AGACAACTAATTAGA[A/C]CTTCTTTCCGGGTCC | 114088 |
rs537857200 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036172 | TGAAAACCTGCCATG[C/T]TGATGAGCCAGCCCA | 114088 |
rs537882940 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075892 | TTGCCAGAGAACATA[A/C]AACCTAAAAGGTGAT | 114088 |
rs537913440 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068676 | AGACACTGTTTTGCC[A/G]CTATGGGTGGGTTAT | 114088 |
rs537915685 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977215 | CTCTGCACCCCACCA[C/T]GGCTGGCTGAGCTCC | 114088 |
rs537921765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070377 | GTGACCAGAGGCTCA[C/T]AGGAACCTAACCCTC | 114088 |
rs538036809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074567 | CAAATCTTACTTCTC[A/G]TTTTAGGAAGTAAAT | 114088 |
rs538037118 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081724 | ACGTTTGATAATTCA[C/T]TAGAATGACTCACAG | 114088 |
rs538041948 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988451 | AGTAACTTGGCATTA[A/C]GATGGTTATGGCTCT | 114088 |
rs538070111 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048978 | GACAGCATGAGACTC[C/T]ATCTCAAAAAAAAAA | 114088 |
rs538073717 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080997 | AATTTGCAGTAGGTC[G/T]TGATAGGCCAGTCTT | 114088 |
rs538149783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043148 | TCTTGTACTTAGAAT[A/G]TCACCTTTTGCTCAT | 114088 |
rs538160773 | snp | A/G | 3.33656e-05 | 0.00408432 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979343 | GGCAGCCTTTGAACC[A/G]GTAGCCAGCAACAGC | 114088 |
rs538170929 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090227 | AAAACATGAACATAT[A/G]CTGCCTGTTACATTT | 114088 |
rs538174637 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981398 | TTCAGAAGATTCCCA[C/G]AAGGAAAAATTTTAT | 114088 |
rs538180718 | in-del | -/TCTT | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993752 | GGATAGTTTTCCCTC[-/TCTT]TCTTTCCATTTGGTT | 114088 |
rs538199359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029627 | TACAATCAAAAAGTG[C/T]AAGCAAGAAATTCTA | 114088 |
rs538235323 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982593 | TTGAAGTCTTCCTCG[G/T]CTCTAGTGAAAGCTC | 114088 |
rs538282681 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990191 | CCTGGCCAATTTTAA[A/T]TTTTTCTGTAGAGAC | 114088 |
rs538292473 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022137 | TATTGCTATGGTTTG[A/C]ATATCTCTTCCAAAA | 114088 |
rs538297920 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053428 | TTCATTCAGTACTCA[G/T]TTTGTATCAGTTTGT | 114088 |
rs538317912 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044429 | TTAGCCACTGAGATG[C/T]AGATGATGTTTTTGA | 114088 |
rs538338209 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024856 | AGGAAGGAAATGAAG[G/T]AAGAAAAGAAGAGAA | 114088 |
rs538350213 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023237 | ACAAAGCTTTAGTTC[A/G]TAGAGTTGTTTATGA | 114088 |
rs538410277 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033443 | ACATACATAAATCAC[A/G]AAAACACTTTTGTCA | 114088 |
rs538428345 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003338 | TCCTTATTAGTTAGC[A/G]CCCACCATGAAACAA | 114088 |
rs538447456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040183 | TTCCTCGGATGGTCT[C/T]ATATTTTCAGTTGGA | 114088 |
rs538482932 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096698 | TGTTATTTAAAGCCA[C/T]GTTAATCATAAATGT | 114088 |
rs538489362 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002718 | TCTATGGCAGATAAC[C/T]TAGAAAACAAAAGCA | 114088 |
rs538497421 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997812 | ATTTAGATTGTTATC[A/G]AAGGAAGCCGCCGGC | 114088 |
rs538520975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034303 | CTTCACAAATAAACC[C/T]AATGAGAATTTAGGC | 114088 |
rs538556603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027472 | TATTTGTTTTCTTCA[C/T]TCTTGCTCACACAAA | 114088 |
rs538558660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073678 | TGCAGGGGGCTTCTG[A/G]AGGCTGATGATATCC | 114088 |
rs538563221 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997314 | CCAAAATATTTAAAG[C/T]ATAGCTAAGAAGCAA | 114088 |
rs538608789 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067465 | TGCTTAAGACACTCC[C/T]ATGGCCTCCTACTAC | 114088 |
rs538629578 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989252 | ACATTGAGAACAGTA[C/T]TGCCACTCCCTGGTT | 114088 |
rs538636106 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082329 | CAGCATTATTAGTAA[C/T]AGCCAAAAAGTGGAA | 114088 |
rs538641407 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028117 | AAAGAGTTTTGGCCC[A/C]ATCTAGTCCCAGGAT | 114088 |
rs538700869 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982551 | CAGGAAATATCCCTT[C/T]GGCAGAAGTGCTAAC | 114088 |
rs538705952 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008216 | TATCCCGATGCAGTG[G/T]TGATTATAGGAATCT | 114088 |
rs538727613 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016047 | TGTGGGGGATTGATT[C/T]CACGATTCCCTGAGG | 114088 |
rs538761025 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975077 | ACTGGACATTTCACA[C/T]CAGGTTAAATTTCAT | 114088 |
rs538817219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994435 | GTAGAAAGGTCAGAA[A/G]GAGATTGGAAGATGC | 114088 |
rs538823813 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002106 | TGGGAACCATGGTTT[C/T]GTGTGTGTGTGTGTG | 114088 |
rs538827297 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080410 | TCCCCAGAAGGGAGA[A/C]TAGGTGTTTCAATTG | 114088 |
rs538871743 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086689 | GTTAGAATACAGATA[G/T]GGACGCTATGGAGGA | 114088 |
rs538873348 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047988 | AATCCCCTTACCAAA[C/T]CCGTTAAGTGCATAG | 114088 |
rs538876664 | snp | A/C | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095633 | CCCGGGCCTAGGCTT[A/C]TGCACGGCAGTGGGG | 114088 |
rs538890296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074357 | AACAATCACTTGAAA[C/T]TGAAGAATTTGGCAT | 114088 |
rs538912272 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095397 | GATGATTCATCCTCG[C/G]CCGGCTTACTTCCGA | 114088 |
rs538998556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035583 | GCTTATCTTAAAACT[A/G]TTCCCTGGTAGTTTC | 114088 |
rs539085590 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068796 | CCAGGCACCTGGCAC[C/T]CTAGAGCAACTGTTC | 114088 |
rs539094485 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011558 | CCCAATATTCATACT[A/G]CTTTGCAAAAGCCTA | 114088 |
rs539111948 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071270 | AATCCCAGCTACTCT[G/T]GAGGCTGAGGCAGGG | 114088 |
rs539150383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005101 | AAGCTATTACCGGTA[C/T]ACTGTTAAAGATAAC | 114088 |
rs539185961 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095846 | CCGATGGAAATGGTC[A/G]GCATTAGTCAGAATC | 114088 |
rs539214829 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093293 | TCCCAAAGTTTGCAC[A/C]TATAACTACTGAAAG | 114088 |
rs539233109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069562 | CAAATCCGAGGCCCT[C/T]GGGACAAGCCAGGCA | 114088 |
rs539262931 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016479 | CCCACCCCCTACCCC[C/G]CTGCAGCTCTCTCTC | 114088 |
rs539274959 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026304 | GAGGGGAAGGAGCTC[A/G]GTTCTGATGGCATCT | 114088 |
rs539292913 | in-del | -/ATT | 0.0107246 | 0.0724382 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016541 | TAATAACACAATAAC[-/ATT]ATGTTATTATTAGCA | 114088 |
rs539324536 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077344 | AAGGCGACCATGAGC[G/T]GTCAAACTTAAGTCC | 114088 |
rs539344591 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053232 | AAGAAAAACGCAAAA[A/C]GAATCTTAAAAAATG | 114088 |
rs539344937 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048568 | CCTCAAGAAGCTGGG[G/T]ATCCTAGGCACATAA | 114088 |
rs539355972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067984 | ATAGCAGGCATTCAA[C/T]TGACACTTGCTGAAT | 114088 |
rs539484707 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026074 | TCCAGCCTCCTCGTC[C/T]GCTGGGGAGGCCGTG | 114088 |
rs539499490 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058216 | CATTACAGGATGGCA[A/C]AATCATGGAACTCAG | 114088 |
rs539501713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050731 | TCTTCTCCCTCACTC[C/T]CTCTGTTTTTCCCTC | 114088 |
rs539550300 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043473 | TGAAATGCCTGTTGG[C/T]CCCATAAACACACTT | 114088 |
rs539552943 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083337 | GCTCACTGTAATCTC[A/G]AACTCCTGGGCTCAA | 114088 |
rs539620389 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061809 | GTTCTGTAAGCTTTT[C/T]GGATCTGTGAGTTGA | 114088 |
rs539656279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024116 | CATTTAAGAGCTCTC[C/T]ATGCCACATGCAGGG | 114088 |
rs539686859 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026130 | TAAGTGGAAGTCTGC[C/T]GGGGACTGGAGGGGT | 114088 |
rs539687589 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039808 | CTGGAGTGCAGTGGC[A/G]CGATCTCAGCTCACT | 114088 |
rs539699483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055494 | ATCAAAATGTAATCA[C/T]AAGTCTCTTAAAAGT | 114088 |
rs539722130 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031165 | AAAAAAAAAAAAAAA[A/G]GAAAGAAAAGAAAAG | 114088 |
rs539722442 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041982 | CTTCAGAACAATGTG[A/G]CTCACTGCTGGAGCA | 114088 |
rs539732066 | in-del | -/A/AA | 0.497984 | 0.0316851 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059797 | GTGAGACTCTGTCTC[-/A/AA]AAAAAAAAAAAAACA | 114088 |
rs539748198 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998242 | CCCCTTCTGAGGGGC[A/G]AGGGAGGCAGTGTCG | 114088 |
rs539761037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020277 | AGGGGGAGAGGAGAG[C/T]GAGCGAGCCGTGGAG | 114088 |
rs539763288 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037846 | CCTGCAGGACGCCTT[-/G]GGAGGGTAAAAGCCG | 114088 |
rs539782321 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062576 | TATATGTAGATCTAT[A/G]TTTATAGGGGTTATT | 114088 |
rs539786565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054894 | GAGTGCAATGGTGCT[A/G]TCTTGGCTCACTGCA | 114088 |
rs539827636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048708 | CCATCTCGGGGGCCG[A/G]GCGCAGTGGCTCACG | 114088 |
rs539836829 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978340 | AGATGCCCAGCTCAG[A/G]AGGGAAGTGAAACCC | 114088 |
rs539857703 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019028 | GGCTTATCAAGAGAA[A/G]GTGGCATATGTAAAG | 114088 |
rs539877748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010565 | AGCAAACTGGACCAT[C/T]GGAAAGCTTCTTCAA | 114088 |
rs539887984 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081950 | GTTTTTATAGAACTC[A/C]ATCTCCAGCCACCCT | 114088 |
rs539924237 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029600 | CGGTTACTCAGTACA[C/T]TGCTGACATAGTACA | 114088 |
rs539926057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060185 | AGAAACAGCATTTTC[A/G]TCATATTATTTATGT | 114088 |
rs539986674 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042225 | ATCCCTCAAGACCCA[A/G]CCTGTCGTTGTCCCT | 114088 |
rs539990474 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016239 | GGGGTCCTCAACCCC[C/T]GGGCCGTGGACTGGC | 114088 |
rs540051203 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015517 | TTTCTTTTTTTTTTT[C/T]TTTTTTTTTTTTTTT | 114088 |
rs540128939 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054196 | TCTCCCCAGCAGCTC[A/G]GACTATAGGTGTATT | 114088 |
rs540138327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077980 | AATCTCCCTCACTGT[A/G]TGAACGACCCAATTG | 114088 |
rs540154720 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983955 | CGAATGTGTTAAAAC[G/T]GCCTCCTTTCCTTCT | 114088 |
rs540203095 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096153 | ACGTGCCCTGGGCAT[C/T]TGCCATAGCTTACAG | 114088 |
rs540209040 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097333 | CACCCTGTTCCAAAC[A/G]GGGGATTTATTTATT | 114088 |
rs540218662 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046154 | ATTAGGGATGGGGAC[A/G]GGGGTGATGGGGTGG | 114088 |
rs540278688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088376 | ATTGATACAATATAC[A/G]ATGTGAACTACCTGC | 114088 |
rs540285313 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035196 | CGTAGTGTATTTCTG[C/G]TGAAATTCAGGGCTT | 114088 |
rs540401122 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060568 | ACTTCCAGGGTTCAC[A/T]CCATTCTCCTGCCTC | 114088 |
rs540419438 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068543 | TTCTCACCACAACCT[C/T]GTAGAAGTTATTTTT | 114088 |
rs540450204 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035651 | GTGGCCCAGTGTGGA[C/T]GTGAAGGCAGCCAGA | 114088 |
rs540461563 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076068 | GTTATTAAATACCTG[C/T]AAATGCTGGGCAACT | 114088 |
rs540493181 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062097 | TTATTAAGTCCAATA[A/C]ATAAATTATTTATTT | 114088 |
rs540500278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082449 | AAAAAAGAATGATGT[A/G]CTGAGGCATGCTACA | 114088 |
rs540509979 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009694 | CTCACATTTTAAGCA[C/T]ATCATCTTCATGTGA | 114088 |
rs540519277 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095573 | CTGCGCAGCACGGAG[G/T]ACGCCCCTTCTCTTC | 114088 |
rs540530293 | snp | A/G | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069148 | GAATCAGTCTGAGAG[A/G]GTTGGGCCTTCTTCC | 114088 |
rs540531047 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976916 | TAGCAGGAGAATTTT[A/C]TCCTGGCGGTGCCAG | 114088 |
rs540561173 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053719 | GTCATCTAGCATTAG[G/T]TATATCTCCCAATGC | 114088 |
rs540582859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018459 | AGTAAGCAGTTCATA[C/T]GCCAATAATATCCGT | 114088 |
rs540583906 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982732 | ACTCCTGAAACTAAC[A/T]CGTCAGAAATTTTGC | 114088 |
rs540608351 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029345 | CCAGCTGCCTCCCCG[C/G]GCGTGGGGCACCTTC | 114088 |
rs540694506 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002662 | TGTCAGTCATCCCAA[A/C]CAAAACAGTGTTTAA | 114088 |
rs540719986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011736 | ATCAGGAAATAGATG[A/G]GAAAAAGCAAATACT | 114088 |
rs540727792 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042410 | GATTGGCCAAATACC[C/T]CATTCTCCTTTCAGT | 114088 |
rs540738966 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977647 | AAGACACAGGCCTTG[A/G]TTTTCAGATAGAGGA | 114088 |
rs540789008 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091393 | GAATATGAATGACAA[A/C]TTTTCAGGTCTAGTA | 114088 |
rs540822698 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029064 | CCGCCCAATGCCTGA[C/T]TTGCCCAAGCTGCTG | 114088 |
rs540869260 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989606 | GTTTAACATCACATC[A/G]TATTTCATCACACGC | 114088 |
rs540898913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004733 | GTAAGGTTTTACAGC[C/T]AGTAAGTGGCAGGAC | 114088 |
rs540904103 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024264 | GCACATTTTATGCCA[G/T]CAGAGTAAAGAAAGA | 114088 |
rs540930396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991022 | ATTAATTGCAATTGA[A/G]AAGTGAGAAACAAAT | 114088 |
rs540948879 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083742 | AGTGGAGATGCCAGC[A/G]AGCTTTAGGGTTCAA | 114088 |
rs541063982 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983463 | CTATGAAACAACAAC[C/G]AGGTTGATAAAAATT | 114088 |
rs541080578 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978616 | CCTTCCCAACCACAC[C/T]ACTCATGGGCCCTTG | 114088 |
rs541088199 | in-del | -/GCCT | 0.00874735 | 0.0655527 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018269 | TTGTGAGCTGGGATG[-/GCCT]GCCTGCCTGCCTGCC | 114088 |
rs541096781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026150 | ACTGGAGGGGTCTGA[A/G]AAAGCTTTTGCTTTT | 114088 |
rs541116237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032558 | CCCAGATCTAGAACT[G/T]GTAGTAGGATTGGTT | 114088 |
rs541128987 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063677 | AAGGAAAGATGGTAA[G/T]GGAATCAAATTTTTA | 114088 |
rs541147986 | in-del | -/TCATCTTTGG | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061834 | AGTTGAAGTAACTCT[-/TCATCTTTGG]AAAATTCCAAGCCAT | 114088 |
rs541239942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019840 | AAGTGTGTCCTCTCA[C/T]CCCAGCCTCTATGAC | 114088 |
rs541261605 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012822 | TGGTGATGCTGAGCA[G/T]CTTTTCATACGTTTA | 114088 |
rs541264267 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051617 | TGCAATTAGCTATTA[A/C]TAAATCACCCTAAAC | 114088 |
rs541288581 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080722 | AGTGACTTTTTTGAA[C/T]ACTGCCATGGTAACC | 114088 |
rs541304439 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030201 | AGAGATTGGGTGAAG[C/T]GGGAATTAAGTAAAG | 114088 |
rs541320310 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037264 | CAGAGAGCCACTTTA[C/T]ACAAATGTATTGCTT | 114088 |
rs541332848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076966 | TGGTTTTATTAGGAG[A/G]AGACCTCTTCAGACG | 114088 |
rs541363103 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044395 | AAAAATAATTTCTGA[A/G]CCTCCTCTGCAGCTA | 114088 |
rs541363149 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036594 | AATGTAAGTACTATG[C/T]AAATAATTGTTACAC | 114088 |
rs541382679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000195 | TAAATCTTGGACAAC[A/G]GTTAATTATATTATT | 114088 |
rs541399173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050991 | GCCAAGATGCTGCTG[A/T]TTCCTAAGCACAGAA | 114088 |
rs541448271 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990954 | CACAATTATGTCCAA[C/T]TGGTACATAATTTAT | 114088 |
rs541458713 | snp | C/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979082 | GCCAGTTGGTTAAAG[C/G]CTTTCGTTTCTATTT | 114088 |
rs541467132 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074935 | AATGTTGAAGCCCCA[A/G]TTGAGAAGCTTGAAA | 114088 |
rs541487540 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084771 | CTAGGTAATGGACTA[C/T]ATATATCTAGTAAAG | 114088 |
rs541489705 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072535 | CCAATAAAAAACAAG[-/T]TTTTTTCTATTGAGA | 114088 |
rs541502585 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025208 | GAAGGAAACTCTCCC[A/G]CCACACAGTTACGTA | 114088 |
rs541589669 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988355 | CCTTTTCTATTCTCA[-/G]CACCAAGAAGAACTT | 114088 |
rs541601747 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029924 | TTAATTGTTTAATCC[A/G]CGGTGAGAGCATGTA | 114088 |
rs541695239 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045264 | TATATGGGACAGAGT[A/G]AGATATCAGAGTCAT | 114088 |
rs541845574 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999510 | TATCAAAAGAGAGAA[C/G]CTTTGTCCTTGAGGA | 114088 |
rs541885231 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005367 | TAAGGGGATTAACAG[C/T]CAATGGTCTATGTGC | 114088 |
rs541888477 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030722 | TTGTATGTGAGATAT[A/G]TCATCAGTGGAGTAT | 114088 |
rs541910567 | in-del | -/A | 0.117188 | 0.211804 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995773 | CCAATACCAGCAAAG[-/A]AAAAAAAAAATCTCT | 114088 |
rs541919972 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038213 | GGGAGATGTGATGAC[A/G]GAAGAAGGATCAGAG | 114088 |
rs541977360 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084663 | AATGCTCTTGGGATA[A/C]CATTATTCCAAGATA | 114088 |
rs542024455 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006710 | TACCAAATGGCCTGT[C/T]AGGTTAACTTCATGA | 114088 |
rs542052764 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063504 | CTGAACTCCAAGCAG[A/T]ATAAAATTTTCAAAA | 114088 |
rs542122605 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049836 | TCTCAAAAAAAAAAA[A/T]AAAATAAAATAAAAA | 114088 |
rs542149724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012709 | ATTTCTCCACATCCT[C/T]GCCCACACTTATTAT | 114088 |
rs542189586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049618 | GGATCATGAGGTCAG[A/G]AGTTCAAGACCAGCC | 114088 |
rs542203460 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092465 | CAGTTGGCCACTTGC[A/G]AAAGCTACCCTTTCT | 114088 |
rs542209916 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999183 | GGACCGCACTTTTGA[A/G]TAGAGGAAAAAGTCA | 114088 |
rs542212381 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066024 | GATTATTTTCATTGG[C/T]GTGCAAGCAGGCCTG | 114088 |
rs542238723 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013115 | TCCAGTGTCCCAAAG[G/T]GTTCCCCCTGTGTTC | 114088 |
rs542243023 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037523 | AAAGAAAGAGGGGGC[-/T]TTTTTTGCACTTAAG | 114088 |
rs542255541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058536 | GTGGGGAGTGGGACA[C/T]GCATCCTCCAGGCCA | 114088 |
rs542287148 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091748 | ACTGTTTTGGAAAAA[A/G]TGTGCAAAAGATCAG | 114088 |
rs542303718 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985079 | ATGAAATGTGCATCA[C/T]GTGTATCCATGATTA | 114088 |
rs542344325 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999738 | CAGGAACTGGCCTCA[G/T]TCCCCAGAACGGCTG | 114088 |
rs542406070 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071551 | ACACCTGTAATCCCA[C/T]CACTTTGGGAGGCCA | 114088 |
rs542406421 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072161 | AGGTTCCAGGAATAG[C/G]CTCAGTTCTTTCTGG | 114088 |
rs542433479 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985671 | TGTGATGACAGAGCG[A/G]GTTATCCATGGTGGT | 114088 |
rs542473097 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070780 | AGAAAAATGGCACAG[A/T]GTATTTGTTTCTGAA | 114088 |
rs542478314 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057640 | ATAGGCAAAAATATT[A/C]TTGCACATTATAAAT | 114088 |
rs542488559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078281 | TGATTTAATATCTAA[A/G]GAAAACTATGAGATA | 114088 |
rs542532798 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072191 | GAACATTCCAGGAAA[C/T]GTATTTCTTTTTTTT | 114088 |
rs542598316 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021389 | AGGTACTCTGTGACC[A/G]TTTTAACTGCAAGTA | 114088 |
rs542661542 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020938 | CCAGGAAGTGTTCGC[A/G]ATGTTTCAAAAGAGA | 114088 |
rs542684913 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096956 | GAAAGGAGTGTCCTT[C/T]TATGGCTTTTGTATG | 114088 |
rs542690607 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022314 | TAAAAGGTTGAAGTT[G/T]GGCTCTTATCCTCTC | 114088 |
rs542723281 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009047 | CATCCACTCAGGATG[C/T]TGCTCTCTGACTTGG | 114088 |
rs542746655 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066738 | GAAAATGGAAATGAG[A/G]TGCAGAAAACGGAAG | 114088 |
rs542764590 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078765 | AAAATGAAGGAGATG[A/T]AAGTCCAATAATTCA | 114088 |
rs542776479 | snp | A/G | 1.64969e-05 | 0.00287196 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000734 | AATGTATCCATCGGC[A/G]GGCACCGTGGACAGA | 114088 |
rs542812325 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086250 | GACAGCCAGGATTCA[A/C]ACTCTGACCCTGCCA | 114088 |
rs542838494 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085286 | AATTAACCATCTACA[G/T]GTACTCCTGACAGAA | 114088 |
rs542860188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094038 | TGGGATGCGCTGTGC[C/G]CAAGAGACGGGGACC | 114088 |
rs542914271 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033298 | GGGTTTCACCATATT[G/T]GTCAGGCTGGTCTTG | 114088 |
rs542915622 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001337 | CGGGTTCACACCATT[C/G]TCCTGCCTCAGCCTC | 114088 |
rs542932314 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986128 | AAAAGGGAGGGTCTG[C/T]TCTTCTGAATCTGTG | 114088 |
rs542975442 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016107 | TGATATAAAATGGCA[C/T]GGTACTGGCATATTA | 114088 |
rs542992898 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980040 | ATTTGAAAGTCAAAA[C/T]AAGAAGCACTTTTGT | 114088 |
rs543005646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978791 | TTCACTGATGTATCC[C/T]AGACACTTATAACTG | 114088 |
rs543035810 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073933 | CAGTGGTATGCTGGG[C/G]CTGGCTTGTACTGAC | 114088 |
rs543038505 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080653 | TCCAGTGTCCCAATT[C/T]TATCCATTTATAACT | 114088 |
rs543049601 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064183 | AACATAGACTGTGTA[C/T]ATTGACTATGATCGA | 114088 |
rs543059282 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086487 | AAAATACCGGGTTAT[A/G]TTGCTAGTTATTAGT | 114088 |
rs543105200 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974841 | CCCGTCTCTAATAAA[A/C]ATACAAAAAAATTAG | 114088 |
rs543111158 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067682 | TCCTGCAGATCTTCA[C/T]AGAGGGCTGCCCCTT | 114088 |
rs543120606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980915 | GAAAAAGATAAAACA[A/G]TGGGGTCCAATTATC | 114088 |
rs543147041 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027751 | TAAAGGAGGGAAAAA[C/T]GGTCTCATTTGGAAG | 114088 |
rs543159008 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981513 | TGGGTGTTTCAGCAT[A/C]CTGGATTGTTTTCTT | 114088 |
rs543164538 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084499 | CTGAAAGCTGTTTAT[A/C]ATATTTCCTTGCTAA | 114088 |
rs543235952 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007886 | ACCAAGTACAGGAAC[A/G]CATTTAACTGCATCA | 114088 |
rs543304142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040349 | CTCTACCATCTCTCA[C/T]GCCCTTCTCCTCTGG | 114088 |
rs543306620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048451 | AGTTAAGAAAGTTCA[C/T]GTGTTTGTCTGCCTG | 114088 |
rs543307789 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987064 | AGAGGTGGATCTTTC[A/G]CCAATTGAAGCCTTC | 114088 |
rs543326129 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086852 | GTTTCTTGAGACAGG[C/T]GTGTTGAGGAGGGGG | 114088 |
rs543345151 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049512 | TTCATTCAACAAATA[C/T]AGTGTATGTGTAAGT | 114088 |
rs543355743 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017073 | GTTAGATCTTTCTGA[C/T]AAAATAAAGAATTCT | 114088 |
rs543391890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047262 | TTCAAGCCCTAACTC[A/C]AGCATTACCTCCTCT | 114088 |
rs543391944 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040063 | GCTGGGATTACAGGC[A/G]TGAGCCATTGCACCC | 114088 |
rs543477029 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053987 | TACCATCTCTAAAGA[C/T]AGATGAGTGGCCAAC | 114088 |
rs543554016 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057821 | CTTTGATTTTTGAGA[C/T]GAAAACATTCATATA | 114088 |
rs543579315 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006877 | TTACTTTTGTGCGCA[C/G]TCCTAAGTGGCCAAG | 114088 |
rs543619956 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093429 | TCCGGTCCTGACACT[A/C]TAGTCTCAGGTCCCA | 114088 |
rs543644908 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976360 | TCTTTGACCCTTGCC[C/T]ATTTCCTTTCTAGTA | 114088 |
rs543668273 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059252 | TTTCCCTCATGTTAC[C/T]ATGGTTACCACATGA | 114088 |
rs543705875 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037820 | CAGCGGCGTTACCAT[A/C]TATTCCTTAGCCTGC | 114088 |
rs543715237 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038918 | CTAAAGTGGTCCATT[C/G]CAGCTTAACTGTTCT | 114088 |
rs543716973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000243 | GTAATAATAATAACT[A/G]ATAATGAACGCTTGC | 114088 |
rs543721916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992379 | GGCCGGGAGTTTGAG[A/G]CCGGGCTGGGCAACA | 114088 |
rs543784500 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089602 | AGAATCTGAAAAAAA[-/C]GGAGCCTTATCAGCT | 114088 |
rs543784950 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030927 | CAAGGCGGGCGGATC[A/G]CTTGAGGCCAGGAGT | 114088 |
rs543787885 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053651 | GTGCACATTGTGCAG[G/T]TTAGTTACATATGTA | 114088 |
rs543819078 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039842 | AGCTCTGCCTCCCGG[A/G]TTCACACCATTCTCC | 114088 |
rs543829689 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087220 | CGTAGTGGACAGGAA[A/G]GGAGGGGCTCTATGG | 114088 |
rs543855908 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086183 | GGTATGCTTCCTGGG[C/T]TTATCAGAAAGTAGA | 114088 |
rs543870537 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095108 | GCGCTAGCTCTGTGA[A/G]CCGCAGCCGCGTAGC | 114088 |
rs543883904 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078981 | TTTTTCTATCTGTAT[A/C]CCATAACATCATGTT | 114088 |
rs543895744 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980059 | AAGCACTTTTGTTGC[A/C]CCTAAACCACATGCA | 114088 |
rs543946374 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047996 | TACCAAATCCGTTAA[A/G]TGCATAGTAAATGCC | 114088 |
rs543982409 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995025 | TTTCCTTTTCTCTGT[C/T]TCTTTTTTTTAAGAT | 114088 |
rs544014658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051493 | CAGGCAGTCTTACCT[C/T]GTAGGCCTTTGCTAC | 114088 |
rs544025501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014123 | GAATTGTTGTGTTTC[C/T]TTTCCAGAGGATTCA | 114088 |
rs544051971 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046460 | CACTGGGAGAAACTG[C/G]GAAAAGTGTCGAAGG | 114088 |
rs544114613 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992793 | TGAGAGTCTAATCGG[A/G]GAGAAAGACATTTTA | 114088 |
rs544120174 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014835 | GGCTCTGATGTGCCA[A/G]AGAACCCCTTGGCAT | 114088 |
rs544124757 | in-del | -/TAT | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064712 | TTAAAAGGATAATAA[-/TAT]TATTAATAGCTTTAT | 114088 |
rs544163058 | snp | C/G | 0.00517822 | 0.0506191 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095522 | TGCGTTTGGCTCCCA[C/G]CTCTGAGCTCCGCGC | 114088 |
rs544198517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009517 | CATGCTATTTATGAC[A/G]GATTTACTAAATGCC | 114088 |
rs544251491 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041113 | TTTTCCCTCAGCATC[A/G]TTGTCAATCCATTTC | 114088 |
rs544275734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088279 | TGGCACTCTAACAGA[A/G]TTTCCAAAGTTAGAC | 114088 |
rs544282769 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096409 | ATTTGAAATAGTACA[C/T]AGCCGGCTTTTGCTG | 114088 |
rs544284943 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975596 | AAAGATTGTAACTGA[G/T]AGAAATAATCTAAAT | 114088 |
rs544352010 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022279 | GGAGTGGGTTAATTA[A/T]CATGGGAGTGGGCTC | 114088 |
rs544358673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074886 | GGGAATGAAAGATGC[C/T]GCAACTACATGGTTC | 114088 |
rs544367578 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084318 | CAAGTTCCTACATTC[C/T]ATATTTCTTGATTCT | 114088 |
rs544371897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017811 | AAAGTGAGTGGGGGG[A/G]CTGTTCAGGGGTGTG | 114088 |
rs544417188 | in-del | -/T | 0.492727 | 0.0598633 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001229 | AAGCTGTGCTAATAA[-/T]TTTTTTTTTTTTTTT | 114088 |
rs544445393 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980294 | TGCCATTTTACAAAG[A/C]ATTGTGTCTTATGCT | 114088 |
rs544455291 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975448 | CCACGGCCCAGCCAT[C/T]GAGTCTCATTGGAGA | 114088 |
rs544498557 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042154 | TCACTCCAGCATGAT[A/G]ATGCATTATGCTAAG | 114088 |
rs544507254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059984 | GATACAAATTGTTTC[C/T]TAAAAAAGTGTTTTA | 114088 |
rs544588826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061256 | TGTCTCTACGAAAAA[C/T]ATAAAAGTTAGCTGG | 114088 |
rs544596885 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067929 | AGCAGAGAAAGTCTT[A/G]TGTATTGTTGTATGC | 114088 |
rs544600788 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989351 | CCATGGGATGCAGGA[A/T]GAAGGCACACACTAC | 114088 |
rs544641733 | snp | C/G | 0.00013976 | 0.00835826 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094077 | CAAAACCGGATGATC[C/G]GAGACGCAGGGAGTT | 114088 |
rs544691623 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048760 | AAGGCCGAGGCAGGC[A/G]GATCACGAGGTCAGG | 114088 |
rs544715762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998567 | GGATTGGTACAGTAT[A/G]TAGCCCCTACTGAGC | 114088 |
rs544730537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054482 | GGTGTCATTATGTTG[C/T]CTAGGCTAGTCTGGA | 114088 |
rs544777378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988739 | GAAACACTTTCCAAC[C/T]GATCCCAGCTTAACT | 114088 |
rs544784389 | snp | A/G | 3.29506e-05 | 0.00405884 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000776 | CCAGGACAACGTAGC[A/G]CTGTTGTTGTGGGTA | 114088 |
rs544794359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065209 | GCACGTGCATATTGC[C/T]TCAATATGTGTGAAA | 114088 |
rs544811066 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034725 | ATAAATTATAGAGAC[C/T]TATACAGTGACTTAC | 114088 |
rs544820317 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046739 | TCCCATGTATTACCC[A/G]TAAAACCCTGGGCAA | 114088 |
rs544836592 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021020 | TGTTCCACTATTTAG[C/T]GGGGAAAACTGTTCA | 114088 |
rs544845887 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084546 | TGATGGTCAATAAAA[G/T]CAATAATAGCTGTTT | 114088 |
rs544855477 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979435 | GAAGAGGCCCTCCAC[A/G]TTATCAAATGCTATG | 114088 |
rs544897900 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026795 | CTCTATCCCCTATAA[A/G]TGTGACCTTGAGAAA | 114088 |
rs544900840 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029022 | ACTTCTCACGCTCAG[C/T]AAATGGGTAATGCAA | 114088 |
rs544902376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066100 | GAAGGAGGGAGGGAG[A/G]GACGGAGGGAGGGAG | 114088 |
rs544992944 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007968 | TTTGATAAAAGCATA[A/C]AGGTAGATTTTTCTT | 114088 |
rs544994600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015386 | AGAATTTCATGCTTA[A/G]CCCAACCATGACCTT | 114088 |
rs545042801 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988668 | CTAAGTAGCTGTTAA[C/G]AACAACAAAAAAATC | 114088 |
rs545045602 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074888 | GAATGAAAGATGCCG[C/T]AACTACATGGTTCAT | 114088 |
rs545056293 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014924 | GGAAGGACACAAACA[G/T]GGCCTAGGAGAACAG | 114088 |
rs545070549 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990617 | AGAGGAAAAGCAAAC[A/C]GATTGTGGTTGCTTA | 114088 |
rs545097535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016302 | ACAGCAGGAGGTGAG[C/T]GGCGGCCACCTCCTT | 114088 |
rs545110304 | snp | C/G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072475 | CTTACACAATACATA[C/G/T]GAGGAATTCAATTTT | 114088 |
rs545134704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008528 | TTTCAGCCCCCACCC[A/G]GAATCTCAAAGAGAC | 114088 |
rs545150140 | snp | A/T | 0.0158469 | 0.0875917 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027134 | TGCTGGCTGTTAACT[A/T]TTTTTTTTTTTTTTT | 114088 |
rs545158986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087951 | TATTACATTAATATT[C/T]CTCATGCCTAAAATC | 114088 |
rs545160598 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080730 | TTTTGAATACTGCCA[C/T]GGTAACCCTTAGGAG | 114088 |
rs545170055 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044346 | TCCATCCTAACCCAT[C/T]CCTATATTATTCCAA | 114088 |
rs545174176 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068365 | AACAAAAAACAAACC[C/T]AAATCAATATATGTG | 114088 |
rs545178764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072987 | TCAGAATTAATGTTT[C/T]ATTTATTTTTTTTTT | 114088 |
rs545202308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986888 | TGTTTCTGTTCAGAT[A/G]GTCAGGTTTGGCCTG | 114088 |
rs545252914 | snp | C/T | 0.031825 | 0.122064 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980994 | TATTTTTTTTTTTTT[C/T]CAGAGACACTAATGA | 114088 |
rs545267414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986276 | GGTGCCACACTCAGG[C/T]ATTTACAAAACCAAT | 114088 |
rs545287142 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021459 | CTCCTGGAAGCCCAC[C/T]CTGTACCTATGTTGG | 114088 |
rs545314501 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987980 | TAATTTTTCTATTTT[C/T]TGTAGAAATGGGGTT | 114088 |
rs545381747 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995439 | TCAAGCACTGCCCAA[A/T]AAATAGACAGATAAA | 114088 |
rs545407242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028449 | CTGATGTAGAAGAAC[A/G]TTGTTATTGACTGAT | 114088 |
rs545411427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074801 | CCCTGTGCTTTTCTA[C/T]TTCCCTCTTACAAGG | 114088 |
rs545411972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035319 | AATAAAAAAGCCTTA[C/T]TGACTGTATAGATCT | 114088 |
rs545438603 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069238 | CTCCAGCAGTCTCAG[A/G]AACAGAGAAAGATGA | 114088 |
rs545476905 | snp | A/G | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029396 | TGCCATTCAGGCACC[A/G]CAACACCACTGGGCC | 114088 |
rs545482919 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061176 | CCAGCACTTTGGGAG[A/G]CCGCAGCAGGTGGAT | 114088 |
rs545484765 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053831 | GAACAGGTATTCTTA[C/T]GGATGGTAAGAATTA | 114088 |
rs545502032 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081202 | GACTTTAAATAGACA[G/T]TTCTCTTAAAAAATA | 114088 |
rs545520372 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089712 | TAATTCAACTGAATA[C/T]TCTCTCTGGACCCAT | 114088 |
rs545521544 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060621 | ACAGGCGCCTGCCAC[C/T]ACGCCCGGCTAATTT | 114088 |
rs545566934 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994919 | TAGATGTGCAACTGG[C/T]GTTTTTTCCATGGGT | 114088 |
rs545568014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010656 | CTGCTGGGGATAAGG[A/G]CTCTGGAAGACAGAT | 114088 |
rs545630228 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001392 | CCGCCACCACGCCCG[C/G]CTAATTTTTTGTATT | 114088 |
rs545631302 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016919 | GACTGTACTTTTAAG[A/T]TGCAAGTTTGAAGTG | 114088 |
rs545648261 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049553 | ATAATATAGGCCGGG[C/T]GCAGTGGCTCATGCC | 114088 |
rs545707358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034553 | GGCATTTTGGGAGTA[C/T]GATTTTTTAAATCCT | 114088 |
rs545712820 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063221 | TATAATAAGCATCAA[C/T]TTAATGGGCTTAACA | 114088 |
rs545742408 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040940 | CTGAGAGATCTCAAA[C/T]AGCTTCTATAATAGA | 114088 |
rs545755445 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097025 | TGAGCAGCTGTTACA[A/C]TTTGTATGAGTTTGA | 114088 |
rs545770352 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056466 | CCCAGTGGCAGATAT[G/T]CTATACTCTAGATCC | 114088 |
rs545789439 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008466 | GTTGTTGCATGGTTG[G/T]CTTGAGTTGTTATTT | 114088 |
rs545872546 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982781 | GGACATTAGGTGCAG[A/T]TAGAATGATGTCTTT | 114088 |
rs545897660 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036959 | TCTTTTTACCTTTTA[C/T]AGATTTATATTTCCT | 114088 |
rs545933967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990370 | GAACACCTGTCATGT[A/G]CCAGACATTGCAGTA | 114088 |
rs545934365 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050405 | TGCCTCTTTGCCTGC[C/T]ACCATGTAAGACATG | 114088 |
rs545939937 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076115 | ATTGATCCTGCTCTA[C/T]AACTATAGGAGGTGG | 114088 |
rs545946327 | in-del | -/AG | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087339 | CTGGATAGTTTAAAA[-/AG]AAGGCAAAACCAGGG | 114088 |
rs545948243 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096260 | GGGAGGGAGGGAGGG[A/G]AGAAGGGAAAGAGGG | 114088 |
rs545948693 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016471 | CATTCCCCCCCACCC[A/C]CTACCCCCCTGCAGC | 114088 |
rs545982075 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006940 | AGAGAGCATGAACTC[A/G]CAGTTCCCATACCCA | 114088 |
rs545986003 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062300 | GGCCATCTTTGGGCA[A/T]GCCGTGTAGACTGCT | 114088 |
rs546001161 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054428 | CAGGCGTAGGCCACC[A/G]TGCCCAGCTGTTTTT | 114088 |
rs546039612 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025120 | TGAAGTTGATCTCTA[C/T]GTGTTTGTATGTAAA | 114088 |
rs546059757 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055737 | CAGACTTCTAGCCTA[C/T]AGAATTGTAAAACAG | 114088 |
rs546085847 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002853 | AAACATAGCTAAATC[A/T]AAATTAGTGCCTGTT | 114088 |
rs546175207 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018478 | AATAATATCCGTAAC[A/G]TAAATTTGTGTTCTT | 114088 |
rs546182926 | in-del | -/TTTTTT | 0.00924479 | 0.0673567 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072656 | GTTTCAATTTATTAC[-/TTTTTT]TTTTTTTACTTAGAG | 114088 |
rs546194517 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012586 | ACCCAGAAGTGGAGT[G/T]GCTGGATCATGTGGC | 114088 |
rs546208503 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056934 | ATAGAGATTTCAGGC[A/G]ATATCTTGTACCTGT | 114088 |
rs546231914 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081480 | TAGCATGTGACTCAA[C/T]AATTCCACTCCTAGG | 114088 |
rs546251739 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011872 | CCTTCCCTTTCCCCC[A/T]ACTTAATACTGTATC | 114088 |
rs546269906 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090286 | TTTACTGCTGACATA[C/T]AGTTAACTGAATATC | 114088 |
rs546316944 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003209 | TTCTTTATTAAAATA[C/T]ATTTTTAACATATTT | 114088 |
rs546327198 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005295 | TGCATACTCAGGGCT[A/C]TTATATTCAACTTGA | 114088 |
rs546331140 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087659 | TTCTAAGGTTAAAAA[C/T]TGACCCAAAATGTCA | 114088 |
rs546365556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046914 | GTTGGCTCTTATTAT[A/G]TGAACATTATAAAGT | 114088 |
rs546399795 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024490 | CAATTTACTGGAGGC[C/G]AGAACTAAGGTTATT | 114088 |
rs546403611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034802 | TAGTTCTGAATCTCC[A/G]CTGTGTTTCTTAACA | 114088 |
rs546412377 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069309 | GACCACTGGTTCTCA[C/T]CTGGAGGTGATTTTC | 114088 |
rs546429906 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008937 | AAAGGTAGGTCACAC[A/G]TTTATAAGGATACAT | 114088 |
rs546454837 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053023 | ACAACAGCCAGGTGC[A/G]GTGGTGGGCACCTGT | 114088 |
rs546535224 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067485 | CCTCCTACTACAACT[A/G]AAATAACATTCAAAC | 114088 |
rs546561024 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042252 | CCCTACCCAGCAGAA[A/G]ATAGTTATGGCCAAA | 114088 |
rs546564169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089288 | GATTCTTAAACATTT[A/G]TCTTGTTATAGGTTC | 114088 |
rs546570994 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001656 | CCATCATTTTTTTTT[A/T]AAACCAGTGATTCTA | 114088 |
rs546585137 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988310 | ACAGACCTTGGGGAG[G/T]GTATCCAATCCCATC | 114088 |
rs546588215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034255 | TAACACACACTTAGA[C/T]AGCACTCTATGTGCC | 114088 |
rs546630691 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003127 | CATCACCCAGGAGTC[A/G]TAATTGCAGGATTAA | 114088 |
rs546679807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981289 | CATTCAAATTGGCAT[C/T]CATAAGCTTTAGTTT | 114088 |
rs546680659 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996899 | CTGTTTTCACGGCTA[A/G]GGGCCTTTCATCCTT | 114088 |
rs546697661 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035876 | TAACTGCCTAACAAC[A/G]CACATAAAATGGTTT | 114088 |
rs546705359 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022526 | AAGACACTTATCTTG[C/T]TTATTATTTGTCCCT | 114088 |
rs546723130 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027987 | GAAGCTGCCTGGTGT[C/G]TTGTATTCCAACCTT | 114088 |
rs546778248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060747 | GCTGGGATTGCAGGC[A/G]TGAGCCTCTGCACCC | 114088 |
rs546790733 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086631 | GGGTTCAGTGGAAGA[C/T]TTCTCACAGAAGCAA | 114088 |
rs546802631 | in-del | -/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991744 | AAGCCACAAAGGTAC[-/T]AATTGTAAAGACTCA | 114088 |
rs546816883 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067966 | CCTAAAAATTACTGA[C/T]GCATAGCAGGCATTC | 114088 |
rs546820846 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982329 | AGGGGTTACCTGGCT[C/T]AGACTGCACTCCCAA | 114088 |
rs546829565 | snp | C/T | 5.07773e-05 | 0.00503846 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094364 | GCAGCGCAGGCGGCA[C/T]GGATCGCAGTAGAAG | 114088 |
rs546863185 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014813 | GAATGACACATTTCC[A/G]TGCTTTGGCTCTGAT | 114088 |
rs546863335 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975587 | TAACTAGAAAAAGAT[C/T]GTAACTGATAGAAAT | 114088 |
rs546901529 | snp | A/G | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087369 | GGCCAAACAAAAGTG[A/G]AATGATGTCATGATG | 114088 |
rs546909631 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994355 | GAGGCTGCAGTGAGC[A/T]ATGATTGTGCCACTG | 114088 |
rs546949756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011518 | ATTGAAGAAGGGTTT[C/T]CCAGGAACCATAACT | 114088 |
rs547011197 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018216 | TTTCTAGTAATGACT[G/T]TAGCCAGTCAAATAG | 114088 |
rs547047803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082293 | ATGTCCACATAAAAA[C/T]TTGTATATGAATGTT | 114088 |
rs547063622 | in-del | -/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001750 | GATCACAGTGATCTC[-/T]CCGTTTCAAAACTTC | 114088 |
rs547104611 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994830 | TTTGGGGCTTGGGGG[C/T]CTTATTTGAAAATTT | 114088 |
rs547123076 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977119 | CAGCGGAGGAGAGGT[G/T]GAAAGGGAAAAGGGC | 114088 |
rs547154946 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042643 | TATTATCTTTTTAGG[A/C]TGAAGTCTCTCTTTT | 114088 |
rs547157507 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990585 | GTAGCCTTTGGGGTG[C/T]TATTTTTGGAATCTA | 114088 |
rs547164816 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083449 | TTTTTTTTAGAGATC[A/G]GGTCTCAGTATGTTG | 114088 |
rs547167996 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024228 | TGATGAAGAGGCCCG[A/G]GCAGAGGCAAGCCTG | 114088 |
rs547203578 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085141 | TATTTGGTGCCACAC[A/G]GTTACTTCTTAAAGT | 114088 |
rs547218568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997639 | CCCACCCTCAGAACA[A/G]GCAAGTACTACAGAG | 114088 |
rs547219016 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975029 | AAACAGAAGTAAATC[C/T]CCAATACTTGGAAGC | 114088 |
rs547225967 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076422 | GCTTGACTTTCCCTC[A/G]TTCCCAGGGGAGGGA | 114088 |
rs547238754 | snp | A/C | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022882 | GGGCCAGCAGCTGGG[A/C]TTTTCTTCTGTTGAG | 114088 |
rs547291690 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017032 | TTTGAATTAACTGTG[C/T]GAATTAAAGGGGAAG | 114088 |
rs547315159 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083018 | AAATGAGAATAGTAA[C/T]GGTTCTTGCCTCATG | 114088 |
rs547352904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977421 | TTACACAGTGTACCG[C/T]GGGTGTGTCCCTAAC | 114088 |
rs547361369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055476 | CCAGTAAACACAGAG[A/C]CTATCAAAATGTAAT | 114088 |
rs547380081 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982918 | GTCTTTGCTATTTGG[G/T]AACAGAATAAGGTTA | 114088 |
rs547404860 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063112 | CTTAAAGGAAAAAAT[A/G]ATCATCATGTATGAA | 114088 |
rs547441550 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062425 | AAAGTACCAGTTTCA[C/G]TCATGGTGGAGTAGC | 114088 |
rs547490336 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031073 | AAATCGCTTGAACCT[C/G]AGAGGCGGAGGTTGC | 114088 |
rs547536050 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982447 | TAAAGGGAGAGGGGA[A/T]GCGCTAAGATGCCTG | 114088 |
rs547563364 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074609 | GCCTTTTAATTACTC[-/TT]TGATCCTTCCACCCC | 114088 |
rs547594487 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054790 | GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC | 114088 |
rs547607456 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075773 | GGGAGTGGGTCTGAT[C/T]GATCTGAATTTCTCA | 114088 |
rs547628284 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035987 | TGTATTAGTTTCACG[A/C]CTTCAATCACAATTG | 114088 |
rs547631790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033370 | TGCTGGGATTACAGG[C/T]GTGAGCCACTGTGCC | 114088 |
rs547726090 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044609 | ACTTAGAGAATGGAA[A/G]CTTCAGGCCAAGGAT | 114088 |
rs547804086 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053141 | TTCCAGCCTGGGTGA[C/T]AGAGAGAGACCCTGT | 114088 |
rs547841979 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992011 | TCAGTGGGGACCAAG[G/T]TTTGTGTAGAGGACC | 114088 |
rs547853863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026498 | CTGGGTATACCCTTC[C/T]GTACCTCAGGTACAG | 114088 |
rs547864677 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020330 | GTGTGAGTGGCACTG[A/G]TGGCTGTTTTTGGAA | 114088 |
rs547897433 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019534 | ACTCATGCCACTAAA[G/T]AATCTCCCAGGTTCA | 114088 |
rs547909527 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990972 | GTACATAATTTATAA[C/T]AAAAGGTGGTATTTT | 114088 |
rs547914774 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982368 | TCCGGGAGTGAAGTG[A/G]CATCGATTTTGGAAG | 114088 |
rs547917715 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985756 | ATGGACCACAGCTCC[A/G]TGGTTGCTCCTTCCA | 114088 |
rs547946567 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996787 | TAGCTACCACATCAC[C/T]GTACTCCAAATGGGA | 114088 |
rs547951432 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050452 | ATGATTGTGAGGCCT[C/T]CCCAGCCACGTGGAA | 114088 |
rs548009555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995985 | AAAATAAGCTATTCA[C/T]TATATTTTTTCTTGC | 114088 |
rs548028576 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073441 | AATTGTGAAACATTC[A/G]TAAAAATGGAATACC | 114088 |
rs548028637 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046021 | CGTAATGTATAATAC[C/T]TGAAAATATAATGTT | 114088 |
rs548065998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042604 | GACATTAATTTTACC[C/T]TGATGTTACAAAGGT | 114088 |
rs548083997 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019813 | TCAAGATGAGAAACC[C/T]AGTAAGTGAGAAAGT | 114088 |
rs548116921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991622 | GAATTTTCAGTATCA[C/T]AGGCATAACTTTAAG | 114088 |
rs548135595 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985866 | TCATCCCCCTCACCA[C/G]GCACATGAATGGCAA | 114088 |
rs548142532 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015257 | AGTACACAATACACA[A/G]GTAAAATTTTGTCCT | 114088 |
rs548156220 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982800 | AATGATGTCTTTGTA[C/T]GCATTGTTACGCCCC | 114088 |
rs548234676 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035376 | AAGTCTATCCTTTCT[C/T]AGCACTAATATTTGA | 114088 |
rs548275995 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036757 | GCTGACTGTATATCC[G/T]CTCTCTCACTCTCTG | 114088 |
rs548279132 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990319 | ATGGCACCCAGCCCA[C/T]ATATTTCTTTTATTT | 114088 |
rs548291405 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070490 | TCATTATCTAAAATG[C/G]CTGGGACTGACTGGA | 114088 |
rs548303478 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993604 | AACTCTTGACCTCAG[C/G]AGATCTGCCCAACAT | 114088 |
rs548315716 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076953 | GCAGTCCCCACTATG[G/T]TTTTATTAGGAGAAG | 114088 |
rs548318366 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977084 | AGAATTGTTGGACAT[A/G]GAAGCGGAAGCAGGC | 114088 |
rs548328878 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989034 | CTCTCCAATTGTAGC[A/G]TTACTATCTGGGGCC | 114088 |
rs548338811 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083549 | TGCCCAGCAGAGATC[A/C]TTAGTTTTAAAATAC | 114088 |
rs548367073 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998825 | TGCGTCTTTAGCATA[A/G]GTTAGGCATTTGCCT | 114088 |
rs548394663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983604 | TCTGCTCTTTCAAAA[C/T]GAAAAGCACATCTTT | 114088 |
rs548408203 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081728 | TTGATAATTCACTAG[A/T]ATGACTCACAGAACT | 114088 |
rs548419732 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062637 | GGAAAACCTGAAGAT[A/T]TATTGGCCAGTGGTG | 114088 |
rs548482366 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049895 | CTGGGCAGAGGAAAT[A/G]GCTCTGGTATGTGTA | 114088 |
rs548483857 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043225 | AATTAACTGGAGTTA[G/T]GTATAAAAAGAAGAG | 114088 |
rs548522000 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045311 | AACACAAAATTTATC[C/G/T]TGTGTGTCCCTGTGA | 114088 |
rs548522111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018504 | TTCTTAATACGTGAT[A/G]TAATTAATTTTTGGC | 114088 |
rs548522442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075532 | TTTACACAAAGTTTT[C/T]GGGAACTCATACCCA | 114088 |
rs548530201 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976604 | TGCCTGTGTCTTAGA[C/G]ACTTTCCAATTTTAT | 114088 |
rs548535228 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055219 | TGTAAGACACACCAT[G/T]ATTTTATATTCCAAT | 114088 |
rs548590709 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016212 | TTATATTGTATTGTT[C/T]AGGCAAGGGCAGGGG | 114088 |
rs548663585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991976 | TTATGCCACTGGCCC[C/T]AGGGCACATTTCAGT | 114088 |
rs548664932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025523 | TCTGGTGTCGAAACT[C/T]CCTGTGCTCCTGAGT | 114088 |
rs548680171 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077689 | ATGAGTCACCACTCC[C/T]GGCTGTCCTAAACCA | 114088 |
rs548710740 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037590 | AAGTTCTCAACATCC[A/G]ATAATTTCAGGGTGT | 114088 |
rs548719252 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011940 | AAAATATCCCATTGA[A/G]TGGGTAATCTTAATT | 114088 |
rs548727474 | snp | C/T | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974772 | TTTGGGAGGCCGAGA[C/T]GGGTGGATCACAAGG | 114088 |
rs548751395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004319 | CTTGAAGAGGTCTGG[C/T]GGAGCTGTGGTTCAA | 114088 |
rs548752888 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978287 | CAAGCCTTATCTCAA[A/G]ACAACCATTTGTGGA | 114088 |
rs548754996 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038495 | TGATATTTTGTAAAC[A/C]TGCTCAGAATATGCA | 114088 |
rs548781562 | in-del | -/TTACATTTACAAAGC | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040794 | CTGTTAGTACTAACA[-/TTACATTTACAAAGC]CTGAATTTAAATGAC | 114088 |
rs548789710 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084920 | GTGTATATTTGACCA[A/T]CCAAGATTTTGCCCT | 114088 |
rs548813089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977581 | ATTATATGGTTCTTA[A/G]TCACCTGCCTCTTTT | 114088 |
rs548816785 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071301 | GAATTGCTTGAACCC[A/G]GGAGGTGGAGGTTGT | 114088 |
rs548819249 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048763 | GCCGAGGCAGGCGGA[A/T]CACGAGGTCAGGAGA | 114088 |
rs548842635 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083175 | TCTCATGAAGTGAAT[C/G]TTTGTCTAGTTTTCT | 114088 |
rs548843255 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092616 | AACCATCCTGAATCC[C/T]TGCCCTGCACTCCAC | 114088 |
rs548889014 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004913 | TGAACAATAAAGATT[C/T]CCCAAATAAAGATTC | 114088 |
rs548896216 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063850 | ACAGGAATATTTTTA[C/G]TGTCAAGCGGATTGA | 114088 |
rs548936854 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991062 | AAACCTTCTTTTAGA[A/G]GAATGAAACAGCTTT | 114088 |
rs548940935 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051205 | CAGATAACTATAGGA[A/T]ACCTTCGTTGTTCCT | 114088 |
rs548957333 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068344 | AAAAACAAAAACAAA[A/T]ACAAAAACAAAAAAC | 114088 |
rs548976554 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044774 | CTAAACCTAATCTAA[C/T]TTGTACAAGAGGCCA | 114088 |
rs548977307 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013517 | TACATCGCCCAATTT[G/T]CTGATAGATGATTTG | 114088 |
rs549010810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057176 | CCACAATTCTTTGGT[A/G]GACATTGCTGCTCAC | 114088 |
rs549044250 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015129 | ATTTATAAAGGTCAT[C/T]TCTTGGGTCAGGATA | 114088 |
rs549072490 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046087 | AGGTAAAAATGCAGG[C/T]TTTGGAATGACCGCG | 114088 |
rs549102067 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058757 | CTTCAATTCAGCTAC[A/C]TATGGTGTGACTCAC | 114088 |
rs549103683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021774 | CATCCTTCCTCTCAC[A/G]TCTTGTTGCCCTGCA | 114088 |
rs549110155 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027289 | GCTGGGATTACAGCC[A/G]TGCACCACCACACCG | 114088 |
rs549131937 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025343 | TGACAGTCCGTTCAG[C/T]GCCTGGGAGAGCTGG | 114088 |
rs549149687 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085908 | AGAAGCAGGATGAAC[A/C]CCATCTCTGTCAGGT | 114088 |
rs549191420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000296 | GAATTTTGTATGAAT[C/T]ATCTAATGGACTCTT | 114088 |
rs549198849 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984717 | AAATACATTATCATA[C/T]ATTTAAGATTCAACA | 114088 |
rs549201501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025952 | GTCCTCTCCTCACTA[A/G]CCTCCGACACCAAGG | 114088 |
rs549203090 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018790 | CACATGGAAACTGAA[A/C]GCTAGAATTTTTCCC | 114088 |
rs549225486 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057895 | TGTACACAAGTTTAT[A/C/G]CACTAAAGATCAGTT | 114088 |
rs549262795 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050638 | CTTGGGACTGTCCCA[A/T]CCAAAAGAATATGAC | 114088 |
rs549265135 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003646 | AAAGACCAAAAGGAT[-/A]AAAAAAAAAAGGCTA | 114088 |
rs549277789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985902 | AGACACGCGTTTCAG[A/G]GATGCCTTCAAGGCA | 114088 |
rs549324419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012840 | TTTCATACGTTTATC[A/G]GCTGTTTGTGTACCC | 114088 |
rs549324743 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032155 | CCACAAAAAAATGTA[A/T]CAGACATGCCATTAT | 114088 |
rs549326407 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005124 | AAGATAACCCTGAAC[A/G]CAGGTTTTGAGTCCA | 114088 |
rs549351635 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078556 | GCCACTTGCCACAAC[A/G]TGGGTTATGCTAAGT | 114088 |
rs549376005 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025016 | GTAGAGAATTAGGAC[C/G]TCAGTGTGGAAGACA | 114088 |
rs549391849 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066334 | GTTCTCATTCATCTC[C/T]ATCTTTGCAAACCCA | 114088 |
rs549426670 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073358 | GTGCTATAATGTTTA[C/T]AGCTGCACTACTCTT | 114088 |
rs549449659 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064533 | AAAAAGGAAAGGATA[C/T]AATAAAGACTAGAAA | 114088 |
rs549462197 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059532 | TGGCTGGGCACAGTG[C/G]CTCATGCCTGTAATC | 114088 |
rs549463048 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005656 | AATTAAGTGGAAAAT[A/G]TTTTTTTAATTACTC | 114088 |
rs549548828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983554 | AAACAAAGCCCTTTT[C/T]ATATTATTTAGTTTG | 114088 |
rs549580060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044655 | AGTAACCTAAGTCCC[A/G]GATGACAGTGCAGCC | 114088 |
rs549580888 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023037 | GAGCTCCCCCATCCT[A/G]CTGAAGGGAATGAAA | 114088 |
rs549588802 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067360 | CTCTCTCCTGGACCA[C/T]GACAACAGCCTACTA | 114088 |
rs549602447 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998879 | AAAATTATGCTGATG[C/T]AATGAATAAAAATAA | 114088 |
rs549612172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077061 | GTTAAGCCCTTTCTG[C/G]CATGCTCATTCTATT | 114088 |
rs549652714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986447 | ACTTTTAGAATTGAA[C/T]GTACAAAATGTAAAG | 114088 |
rs549670052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070337 | ATAAAACAAGTTTAT[A/G]CATTGATTGGTTGAC | 114088 |
rs549680352 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014288 | CTGCTGACTCTTAAG[-/A]AGCTTAATTGTTGCA | 114088 |
rs549699622 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032669 | AACTAACTATCTCTC[A/C]GAGTCTGTGTCCAGG | 114088 |
rs549715329 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072626 | AAATCACAATTACTT[A/T]CTTGAGGTTATTGAG | 114088 |
rs549753397 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050005 | ATCACATAGGGATTT[A/G]TAGGCAAGAAATTTT | 114088 |
rs549767385 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077288 | GGTGAGACAGTATAG[C/G]TGACACAGTGGCCAA | 114088 |
rs549768103 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026618 | GTAAAAGGGCAGAAC[C/G]TTAAAATTATATCTC | 114088 |
rs549831642 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063185 | GCATCAAATGGAGAT[A/T]ATAGAACAGAAAAGT | 114088 |
rs549855519 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055094 | CCCAAAGTGCTGGGA[A/T]TACAGGCGTGAGCCA | 114088 |
rs549864398 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064553 | AAGACTAGAAATCAA[C/T]GAAATTGAGAATAAC | 114088 |
rs549968909 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084472 | TCAGCTTCATACTGC[A/T]TTGATTATGTGCTGA | 114088 |
rs549971584 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061532 | TTGATGCTTAAGCTG[G/T]AATTTCTTTAATTTT | 114088 |
rs549985226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013706 | TTCTTCTGACATCCA[A/G]TATGCCTGACAACCA | 114088 |
rs550018942 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032097 | ACATTTACCTCTTTT[A/T]AAATAATAATTTAAG | 114088 |
rs550028770 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035728 | GCTGGTTAGGGCTCT[C/T]CGAAAAGAAAGGGTA | 114088 |
rs550042277 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008022 | TGAATGCTAAGAGTC[A/G]TTTACTATATGGATG | 114088 |
rs550081299 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992084 | AAATAGAGTGTTTAG[A/T]TTATGTAGTGGTTAG | 114088 |
rs550091838 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037860 | TGGGAGGGTAAAAGC[C/T]GTTCTTGTTACATGT | 114088 |
rs550131102 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080133 | AGCAAAACTAAACAT[C/G]AACAATTTTTTTTTC | 114088 |
rs550191955 | snp | C/T | | | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010432 | CACCTCCAAGCAGTA[C/T]TCCATGAGACCTGTG | 114088 |
rs550213394 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030052 | ACCTATGAAACATTC[-/A]ACTTTTTTCCTGCAT | 114088 |
rs550228135 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021140 | TTTTGGGTTTCTGAA[A/G]GGTGCTCAGATTGAA | 114088 |
rs550246367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010593 | CAAACCAGAATCCAT[C/T]CCATTCTGGAATGGA | 114088 |
rs550249318 | snp | A/C/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095326 | TCGCGGCTGCAAGAT[A/C/T]TCTGAAGGGGGCCGG | 114088 |
rs550316715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084866 | GATTATGTCATAGAG[C/T]AATTTGGCTTTGGAT | 114088 |
rs550320036 | snp | C/T | 3.32712e-05 | 0.00407854 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979553 | CCTCCCTCAGTTCTG[C/T]AGGAAAAGAGAAAAA | 114088 |
rs550333234 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045191 | GAGAAATCAGAGACT[C/T]CTTCCCCTGTGAGCA | 114088 |
rs550350640 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026228 | TCCTGACTTTAGGAT[C/G]GATGTGATGTCTTCC | 114088 |
rs550353491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092609 | TCCTTCCAACCATCC[C/T]GAATCCCTGCCCTGC | 114088 |
rs550363261 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034025 | GTGAACTAGATGCTC[C/T]GACCATAATCTATTA | 114088 |
rs550363934 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050913 | AAGCCTTCAGATAAC[C/T]ATAGTAGCAACTGGT | 114088 |
rs550401779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084262 | TTTGAACCATTGTTT[A/G]TCGAGCTTGGTGAGG | 114088 |
rs550472212 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048815 | CGGTGAAACCCCATC[G/T]CCACTAAAAATACAA | 114088 |
rs550506893 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985143 | ATCTTATATATTTTA[A/G]CATTCTATTTGCTAG | 114088 |
rs550512161 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001990 | TACTGTGACTCTTTT[C/T]TAGTACTTAAACTGC | 114088 |
rs550530419 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095715 | TCCCGGGAGTCTGAC[C/G]GCGCTGGCGCAAGCC | 114088 |
rs550534024 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040129 | ATGCGGATAAAGTCT[C/G]TTTATTAAGACCTTA | 114088 |
rs550556367 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086482 | AATTTAAAATACCGG[A/G]TTATATTGCTAGTTA | 114088 |
rs550571071 | snp | A/G | 0.00557542 | 0.0525036 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095335 | CAAGATCTCTGAAGG[A/G]GGCCGGCGTGCGGAG | 114088 |
rs550580931 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020102 | AGAACTCAGCCAAAG[A/G]GAAGCGGAAGAACAT | 114088 |
rs550612533 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046167 | ACAGGGGTGATGGGG[G/T]GGGGGTTGAACCAGG | 114088 |
rs550630212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000917 | ATGACAAGCATCCCC[C/T]TGATAAACACGTGGT | 114088 |
rs550689380 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976749 | GTGATAGATTCATTC[C/T]CCCAAAGCTTAGCTC | 114088 |
rs550768164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014316 | GCACTGCCAAAGAGC[C/T]GGGGAGTTTCAGCAG | 114088 |
rs550784173 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058695 | AGAACAGATATACTC[A/G]GCTGTCTTTTACGTG | 114088 |
rs550816327 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061923 | AGGACTCCAGTGATA[C/T]GTATGTTAGGCCATA | 114088 |
rs550818971 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011384 | ATTTCCAAAGATGGG[G/T]TCCTCCCATGTTGCC | 114088 |
rs550875889 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974958 | CTGGGCCAACATTGC[A/G]CCACTGCACTCCAGC | 114088 |
rs550884494 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000454 | GCAGGCAGTCTGACT[C/T]CAGTACTGCATGTCC | 114088 |
rs550926734 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085851 | TGCTCCATGGTTGAG[C/G]TGGTAAAATCTTACT | 114088 |
rs550938732 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066720 | AGACAGCATTTATGG[A/G]CAGAAAATGGAAATG | 114088 |
rs550982381 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090051 | AAGTGGCAGCATTGG[G/T]TCTATAACCTGGATC | 114088 |
rs550986271 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020935 | GTGCCAGGAAGTGTT[C/T]GCAATGTTTCAAAAG | 114088 |
rs550991048 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047777 | AGAAAACAAGAACAA[A/G]GCTTTCAATTGGGGG | 114088 |
rs550992897 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053894 | AAATGAAAAGAAATA[C/T]ATTATGGGTAAGAGT | 114088 |
rs551029854 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053210 | ACTATCTATAGAGTA[A/T]AAACAAAAGAAAAAC | 114088 |
rs551070226 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993438 | GAATGGTGCAATCTC[A/G]GCTCACCGCAACCTC | 114088 |
rs551132433 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081925 | ACTTTCCAAATCTTG[C/T]TGTTCAAGAGTTTTT | 114088 |
rs551174848 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045592 | AATGTAGCATAAATC[C/T]ACATTGGTAAAGAGT | 114088 |
rs551201662 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027928 | TAGTAACCACACTTA[A/G]ATGTTTCAGTACAGA | 114088 |
rs551252497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093112 | ATGAGGTCGAAGGGG[A/C]CAAAATGGAAGAGGT | 114088 |
rs551269654 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071666 | AAAAAATTAACCAGG[C/T]GTGGTGGTGTTTGCC | 114088 |
rs551278300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060216 | GGTGAGAATCTCAAC[A/T]TTCTTATTTTGTAAT | 114088 |
rs551323853 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015763 | CTCCAGCCTTGGCCC[C/T]CCAAAGCATTGGGAT | 114088 |
rs551364253 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090630 | TTGAGACAGTCTTGC[A/T]TCGTCACCCAGGCTA | 114088 |
rs551432687 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007141 | CTCCTCCTGCCCCCT[C/T]ACTGAGGCTAATTGG | 114088 |
rs551449226 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040081 | AGCCATTGCACCCAG[C/T]CAAACTTTTAAATAT | 114088 |
rs551451017 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032690 | TGTGTCCAGGGAACC[A/C]AGTCTAAAATACTAA | 114088 |
rs551504969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022416 | AACACCATGCTTTTG[A/G]ACTTCCCAGTCTTCA | 114088 |
rs551519407 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067210 | CTTAATACATAGTGC[C/T]ATTATTTAGCCCGTT | 114088 |
rs551543478 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987217 | AGGGTATTTCCGTGA[A/T]TTTTTTTCTGGTTTG | 114088 |
rs551546642 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092368 | GGGTTAAGGAGTTGA[G/T]AAAACTTTCACTGAT | 114088 |
rs551564732 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013648 | AAGATTATTTTTGTG[A/C]GTTTTGGGGGGATCA | 114088 |
rs551701411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014187 | CATTACTCAGTCCTC[A/G]TAAAATTCCACATTT | 114088 |
rs551796252 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052602 | TCATCTTTTCAATGA[A/T]ATGAGCCTCTGATTT | 114088 |
rs551834884 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059655 | ATACAAAAATTAGCC[A/G]GGCGTGGTGGCACAC | 114088 |
rs551857226 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046818 | ACAGGATCCACATCA[C/T]GGAGCTGTGAGGATT | 114088 |
rs551870227 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055766 | AGGATAAATTTGTGT[C/T]TGTTCAAGCTACTAA | 114088 |
rs551898461 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029097 | TGTGCCCAGGCAGAA[C/G]ACAGTATCTTCTTTC | 114088 |
rs551900948 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983941 | TAATAATGACATGAC[A/G]AATGTGTTAAAACTG | 114088 |
rs551908904 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053119 | GAGCCGAGATTGTGC[C/T]ACTGCATTCCAGCCT | 114088 |
rs551912334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073444 | TGTGAAACATTCATA[A/G]AAATGGAATACCATA | 114088 |
rs552007898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068659 | AGCCTAAGCTCTTGG[A/C]CAGACACTGTTTTGC | 114088 |
rs552019553 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033335 | TGACCTTGTGATCTA[C/T]CTGCCTCGGCCTCCC | 114088 |
rs552033885 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027203 | GGCTGAAGTGCAATG[G/T]TGTGATCTTGGCTCA | 114088 |
rs552034674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021955 | ATCATGCTCATTTTC[C/T]AGAAAGTACAGATTC | 114088 |
rs552074567 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093089 | GCAGAGGGAGTAAGT[A/G]GGAGGCAATGAGGTC | 114088 |
rs552096262 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034313 | AAACCCAATGAGAAT[A/T]TAGGCCTTAACTAGG | 114088 |
rs552098585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027342 | AGAGATGGGGTTTCT[C/T]CATGTTGGCCAGGCT | 114088 |
rs552113001 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067994 | TTCAATTGACACTTG[C/T]TGAATACATGAATTA | 114088 |
rs552124636 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083088 | TTAGATCAGTGCCTA[C/G]ACCACTATGTACTTG | 114088 |
rs552181269 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998691 | CTTCAGAACTGTCAC[A/G]GAGATTACACTCCAA | 114088 |
rs552222784 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074069 | AACAGAGACAAAAAC[A/G]AAACAATCACTGAAT | 114088 |
rs552231067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083453 | TTTTAGAGATCAGGT[C/T]TCAGTATGTTGCCCA | 114088 |
rs552233518 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016480 | CCACCCCCTACCCCC[C/G]TGCAGCTCTCTCTCT | 114088 |
rs552260544 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035775 | GATCTATTCTGTAGT[C/T]CATCTCTGGAATGTA | 114088 |
rs552271319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043121 | GTTTTGTGACAATTG[C/T]CTTCCCAAATGTCTT | 114088 |
rs552372634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080902 | GACTTTTCCATGTTT[C/T]CTGTTTGTCAAAGCC | 114088 |
rs552381098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001800 | CTCTCAAGGTAGCTA[C/T]ACCTCGAAAACAGCA | 114088 |
rs552388997 | in-del | -/G | 0.00755907 | 0.0610114 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997102 | GAATCCCGGTGAGGT[-/G]GGGGGGGTGATTTCT | 114088 |
rs552400359 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990622 | AAAAGCAAACAGATT[A/G]TGGTTGCTTATGATA | 114088 |
rs552410686 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989196 | CTCCTGGTCATGCCC[A/T]CTGGACATGTTCAAA | 114088 |
rs552508445 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988445 | GGGATTAGTAACTTG[C/G]CATTAAGATGGTTAT | 114088 |
rs552515289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017341 | AATCGAGAAAAGGAT[A/C]ATTTAGGCCTTTAAA | 114088 |
rs552578249 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026487 | CTCCTAGCAGTCTGG[G/T]TATACCCTTCCGTAC | 114088 |
rs552634056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991786 | CTGTAAGTCCATGGT[C/T]TTAGAGATGAGAAAA | 114088 |
rs552639195 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051109 | AGATTTAACTCTAAG[C/T]ATGATGAAAAGTCAT | 114088 |
rs552639316 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077358 | CTGTCAAACTTAAGT[C/T]CTGGCCCTCAGTCTC | 114088 |
rs552645648 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059097 | ACCCCAATATCAGCA[C/T]GAGCTTCCCTGCTTT | 114088 |
rs552660074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036662 | TGACATGATCAGTAC[A/G]GGCTCAATTATTTTT | 114088 |
rs552661730 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980499 | AGGTTTACAAATTGC[C/T]TCTTGCTACTTCACA | 114088 |
rs552693962 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061142 | TGTTGGCTGGGCGTG[A/G]TGGCTCACGCCTGTA | 114088 |
rs552704925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027437 | GTGTGAGCCACCGTG[C/T]CCAACCAGCTGTTAA | 114088 |
rs552728565 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039394 | ACAGCTCAGATGTCT[A/G]CCAACAGTAACATGC | 114088 |
rs552757195 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028095 | ACAATCATTCCTAGT[A/G]GTAGACAAAGAGTTT | 114088 |
rs552766488 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001503 | CAAAGTGCTGGGATT[A/T]CAGGCGTGAGCCACC | 114088 |
rs552804582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042730 | ATGGAGGCTTAGTCT[C/T]ATTTGCAGGTAGGGG | 114088 |
rs552818439 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052615 | GATATGAGCCTCTGA[C/T]TTAAAGTAGGAATTC | 114088 |
rs552824244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072858 | GAGCAATGTACCGTG[C/T]AGGAGATGATTTGCA | 114088 |
rs552843280 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048877 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 114088 |
rs552862899 | snp | G/T | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096661 | AGTAGTTGATCATTG[G/T]GTGGGGGAATAAAGT | 114088 |
rs552870189 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032404 | AATATCAGCTGTTGA[C/T]AGATTACCCTAGGAA | 114088 |
rs552902866 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065677 | TGGCCATAGAGGCCT[A/G]GAGTTGGGATTCACT | 114088 |
rs552904397 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996221 | AATTCATGGAGGAAA[C/T]TAATTTCTACAGTAC | 114088 |
rs552918809 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988634 | ATTACCTACCAGCTG[A/G]GCTTTTACCGTATTT | 114088 |
rs552982416 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995375 | GGACAGTAGGGATAA[C/T]GTCTGTTCAACACTC | 114088 |
rs553056062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081771 | TTACTTATATTTACT[A/G]GTTTATTATGGAGGA | 114088 |
rs553096224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079338 | AATTCACTCCTTCCC[C/T]GTTTTACAGATGGAA | 114088 |
rs553143396 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086035 | CAATTTCTTTTCTAA[A/G]TTTATTTTGTCACAA | 114088 |
rs553145403 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043084 | TCTGAATTTCTAAGA[A/G]TGTTGTTATTGGACT | 114088 |
rs553176256 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060324 | TTTACTCCCTCAGTA[C/T]TCCTTAGGGCAGCAT | 114088 |
rs553220445 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993158 | TTCCCGGGCAAATCT[C/T]GTCACTGCCAGCCAA | 114088 |
rs553239624 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087834 | ATCTATTTTTGTATA[C/G]CACAGATTAATGAAA | 114088 |
rs553276763 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095376 | CGGGAAGGAGGAGTT[A/T]GGCGGGATGATTCAT | 114088 |
rs553276796 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040065 | TGGGATTACAGGCGT[A/G]AGCCATTGCACCCAG | 114088 |
rs553290966 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997913 | GCAGGAGAGGAACAG[A/C/T]GGCTCTGTGCAGAAT | 114088 |
rs553310731 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034499 | GAAGTACATTCATCA[C/T]CTTCAGCAGGAGTGT | 114088 |
rs553341542 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058707 | CTCAGCTGTCTTTTA[C/T]GTGAAAGAAATAAAT | 114088 |
rs553374821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011073 | GCTTGGGAGAGGTAA[C/T]GAGCTAATGAAAAGC | 114088 |
rs553379433 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041857 | AATAACATTTATATA[A/C]AGAATAATGCCTACT | 114088 |
rs553395972 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047951 | GGCGATACTGTGAGA[C/G/T]CCTGTCTCAAAAAAA | 114088 |
rs553447220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003455 | TACAAAAATCAAAGA[A/G]TAAGATCACAGATGG | 114088 |
rs553474653 | in-del | -/TTAGGTTGT | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015352 | CACAACCAGAAGCAA[-/TTAGGTTGT]GACCTGAGGTTAATT | 114088 |
rs553479906 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049220 | GCATGCGCCATCACA[C/T]CCGGCTAATTTGTTT | 114088 |
rs553516782 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054852 | CCTCTTTTTTTGAGA[C/T]GGAGTCTGGCTCTGT | 114088 |
rs553549435 | in-del | -/CA | 0.00795532 | 0.062565 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994665 | GAGTACAGCTTGTCT[-/CA]CACATAGCATAAACC | 114088 |
rs553561982 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052730 | TTCCTTTTTAGCCCC[C/T]TCTTTTTGACTCCAG | 114088 |
rs553597820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047299 | CTGTCCTTGACTTGC[A/C]CCACCCCAGGTAAGA | 114088 |
rs553627329 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016014 | TTTAAGGTCCGGTAC[A/G]GTTGTCTCCTCAGTA | 114088 |
rs553654841 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975930 | CCATGTTTTTCCAAA[C/T]ATTGTTTGGACTACT | 114088 |
rs553699988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016842 | GAGACTTTTGTTTCC[A/G]AATATTTTCAATCCA | 114088 |
rs553752650 | in-del | -/AGAGAAG | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052069 | GAAGAGAAGAGGAGA[-/AGAGAAG]AGAGAAAAGAAAAGA | 114088 |
rs553782248 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050383 | TCCCCTTTCACTTGG[C/T]TCTCATTGCCTCTTT | 114088 |
rs553798168 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062780 | ATGGGAGAGACTCCA[A/C]GGAGCTCAGCAGAAA | 114088 |
rs553817591 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071942 | GGTGGTGAGGTGCTA[C/T]GCATTTGCCAATCCC | 114088 |
rs553837506 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049563 | CCGGGCGCAGTGGCT[C/T]ATGCCTGTAATCCCA | 114088 |
rs553892779 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090339 | CATTTTGCTACATAA[A/G]TATTTAATGAGATGC | 114088 |
rs553926586 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036265 | CTATGTATTTACACC[A/C]TAGAAATTGGCAAAC | 114088 |
rs553962599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068758 | TGATGAGGCCAGCCC[A/G]TGTTGCAGAACCAAG | 114088 |
rs554030290 | snp | C/G | 0.0178098 | 0.0926698 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995286 | TTTCAGTGTTTATCA[C/G]AATGTGTAAAAATGG | 114088 |
rs554041630 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976712 | GATATTTTTGTGCTT[C/T]AATGAGTAGTAAAAC | 114088 |
rs554089506 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018972 | TTATGTCAAATTGTG[A/G]ATGTTACATAAACAA | 114088 |
rs554123541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061733 | TTTTGTTTTTTATTA[C/T]GTATTCATTTATTTT | 114088 |
rs554142464 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024979 | TTTACAAAAAAATAG[G/T]CCTCTTTCTGAATAT | 114088 |
rs554145573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025637 | TCTCCTCCTTCATTG[A/G]TTAATTAAACAATCA | 114088 |
rs554154869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069955 | CTCACAGCACTTTCA[C/T]GGTCATTCACAGAAT | 114088 |
rs554169904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053655 | ACATTGTGCAGGTTA[A/G]TTACATATGTATACA | 114088 |
rs554183262 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002199 | CGATCTCGGCTCACT[A/G]CAAGCTCCGCCTCCC | 114088 |
rs554186809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070576 | TCAGCATCTCTAATC[C/T]GAAAATCTGAACTCT | 114088 |
rs554195313 | in-del | -/TTTAAGG | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023896 | CACAATTTAAATTTA[-/TTTAAGG]TTTAAGGCACAAATT | 114088 |
rs554201860 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029805 | CACCACTCACATACG[A/G]AACAGCTGGAACACA | 114088 |
rs554252429 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983690 | CATCTTCCAAGTTCA[A/G]TCTTTTCCTCTAAAG | 114088 |
rs554289532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012541 | CAAATATCTTTGTAA[A/G]TCTCCGCTTTCACTT | 114088 |
rs554296166 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061098 | GTGAAGTGTCTGCTC[C/G]AGTATTTTGTCATTT | 114088 |
rs554375353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990775 | TTGGAGCACGGTAAG[A/G]CAAGACATGTCACGA | 114088 |
rs554406124 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010556 | TAGAAGAGAAGCAAA[C/T]TGGACCATTGGAAAG | 114088 |
rs554418056 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083295 | TCTCACTTTGTCACC[C/T]AGGCTGCATGCATTG | 114088 |
rs554433946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077261 | GGAGGATGCAGCCTC[A/G]TGTTTCCCATAGGTG | 114088 |
rs554496048 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988475 | TGGCTCTTCCTATCC[G/T]TCCATGTGGATCCAT | 114088 |
rs554498807 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069704 | CTTGGAAGATCTGCC[A/C]ACCCTGTGCCCATAT | 114088 |
rs554515188 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976836 | TGTATGCTACAAATT[A/C]AGCTCATTCTTCCCT | 114088 |
rs554550610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009651 | ATGAGTTTCATAAAA[C/T]AGTTTAGTGAGGGTG | 114088 |
rs554577607 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992757 | GAAGGAGCTACTACA[A/G]TGAAAGGGGCAGCGT | 114088 |
rs554586471 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076710 | CTATCATTCCTTTCA[C/T]CTTCGCAACAGTCCT | 114088 |
rs554646503 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088958 | TTGGTTGCAAGTGGC[A/C]GGAAACCAACACAAA | 114088 |
rs554654108 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977216 | TCTGCACCCCACCAC[A/G]GCTGGCTGAGCTCCT | 114088 |
rs554686220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002754 | TGTAACATAAGAAAT[A/G]AGAAGGTGAAGCCGG | 114088 |
rs554693846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982652 | ACTAATTTTCATGAG[C/T]GATTGTGACTTGCAT | 114088 |
rs554741769 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994400 | TGACAGAGTGTGACC[C/T]TGTCTCAAAAAAAAG | 114088 |
rs554768329 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981454 | CTGAGGTTCAAAAAA[C/T]GAAGTAACTTGCCCA | 114088 |
rs554810857 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080771 | CAAGAACCTTATGAT[A/G]TTATACTGAGGTAGA | 114088 |
rs554812077 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016153 | TTATATACTTTAAAT[A/C]ATCTCTAGATTATTT | 114088 |
rs554821713 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075912 | TAAAAGGTGATTACA[C/T]AGGAATTCAACAAAT | 114088 |
rs554897532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999366 | TTTTACACACACACA[A/G]CACACACACACACAC | 114088 |
rs554898089 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999498 | ATAAGGCTTCTCTAT[A/C]AAAAGAGAGAACCTT | 114088 |
rs554905599 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062026 | TTATTTCTGAAGTGC[A/G]TTAGATTATTTCTTC | 114088 |
rs554918603 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068234 | CACTATGCCAGGACC[A/G]TGGGGATGAAAAAGG | 114088 |
rs554937647 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029784 | GATACCCCTGAGTGA[A/G]GGTTTCACCACTCAC | 114088 |
rs554946757 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082339 | AGTAATAGCCAAAAA[C/G]TGGAAGTAACCCAAA | 114088 |
rs554953628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990225 | GTCTTTTTATGTTGC[C/T]CAGGCTGGTCTCAAA | 114088 |
rs554960815 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998876 | TGCAAAATTATGCTG[A/T]TGTAATGAATAAAAA | 114088 |
rs554975616 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035634 | CCACCCGGAAGAACA[C/T]GGTGGCCCAGTGTGG | 114088 |
rs555018291 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985477 | TGTGTTTTTACTTTT[A/G]TTGTACTTTGTCAAT | 114088 |
rs555019516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025729 | CTAATTCTTATCAAC[A/G]TTACTTAGCACAAAG | 114088 |
rs555028522 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077437 | TTGCTCTGTTGTCCA[C/G]GCTGGAGTGCAGTGG | 114088 |
rs555043276 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000384 | ACCTGAAGACTCAAA[C/G]GGGTGATAATTAGGC | 114088 |
rs555055698 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072667 | TTACTTTTTTTTTTT[-/TT]ACTTAGAGACTATTT | 114088 |
rs555065160 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018398 | CTCTCTCTCATCTGA[A/C]TCAAAGGATTATTTG | 114088 |
rs555078522 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083737 | ATCCAAGTGGAGATG[C/T]CAGCGAGCTTTAGGG | 114088 |
rs555099468 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989566 | TATAGATCACTAGAG[A/G]AAAATGAGGAGCTCC | 114088 |
rs555119823 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035112 | ACATATAGAGACATG[A/C]ATTATCTCCATATAA | 114088 |
rs555126284 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024873 | AGAAAAGAAGAGAAA[A/T]CTGTGGCCTGTTACC | 114088 |
rs555220120 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996464 | TGATTTTTACCAGAA[C/T]AGTATGATTCCCATG | 114088 |
rs555220299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003371 | CCTTATGCTCTTATT[C/T]CATTAGCTCCATATT | 114088 |
rs555315844 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084403 | TCAATGATAGATTCA[C/T]TTCCATAATGGCAGA | 114088 |
rs555391650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031315 | AGCTCAAGGCTGAAT[C/T]CCTAAGATGACCCCA | 114088 |
rs555405192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046251 | ACTTGTGGGGCTGGA[C/T]CTAGTTATTATCTTG | 114088 |
rs555416919 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004692 | TGCAATTATCTTTAT[G/T]GTGCAGCTGAGGAAA | 114088 |
rs555418315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078074 | ATCAGATGAGCCAGT[A/G]GTCTCATCATCAGTA | 114088 |
rs555481016 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087846 | ATACCACAGATTAAT[G/T]AAAAACTCAATTAGA | 114088 |
rs555508963 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050947 | TGAATGCAACCTCAC[A/G]GGAGACTCCAACAGA | 114088 |
rs555529747 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042559 | GAGAAGAGAGGGAAC[A/T]GTTTTGGTCAGGAAA | 114088 |
rs555530127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056394 | AACTATACTACTAAA[C/T]ACAAAGGTGAATTTC | 114088 |
rs555637403 | snp | G/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979093 | AAAGGCTTTCGTTTC[G/T]ATTTAGAGGTGAAAC | 114088 |
rs555672860 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012263 | CCCCTGGCAACCGCC[A/C]TTCTACTTCCTTTCT | 114088 |
rs555675963 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001611 | GCCTATTCTGAGAAA[C/T]AGCTCTGAAACCACT | 114088 |
rs555701938 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043595 | TGTCACAGAAGTTTA[C/T]ATGAAATTTGGATGG | 114088 |
rs555734882 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013910 | GAGGCTGAACTAACT[A/T]GTTTCCAGGATGACA | 114088 |
rs555756223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004510 | TGTGAAAGTACACAG[C/G]AGTGTGGCAGGGACA | 114088 |
rs555860189 | in-del | -/GCTTCTCC | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038765 | ATCACCAAGAGTGAA[-/GCTTCTCC]GTCAGTCTGGAATCA | 114088 |
rs555870326 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006678 | AAATGAAAATGGAAG[A/G]CTATAATCCAGTATT | 114088 |
rs555884347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043502 | TTAAGCAGTTCTATC[G/T]ACAGCCTATCTGTGG | 114088 |
rs555897827 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093818 | CACTGGCCGCGGCCA[A/C]TGGCTGCAGACCCGC | 114088 |
rs555900811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978538 | CAACTCACTCCCTCA[C/T]TCCTTTAAGGCTCAG | 114088 |
rs555948884 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064001 | TCTAAAAGGCATATG[A/T]TTATTAAAGGCAAAA | 114088 |
rs556029443 | snp | C/G | | | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009117 | CTGGTGGATGGATTG[C/G]AGCAGAGGGCTGTTG | 114088 |
rs556070307 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027030 | GAATACTATTCTTGG[A/G]TTTTGTGGGCATTGC | 114088 |
rs556080748 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011107 | AGAAAGAAGACGGAT[A/G]CAGAATTAAGTTTTA | 114088 |
rs556112763 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064577 | GAATAACAGAAATAT[G/T]TCAAAGTTGGTAGTT | 114088 |
rs556151935 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997363 | CCTTGTATGGTGGCT[-/C]TCGGTAGCCTAGCCA | 114088 |
rs556179467 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031534 | TTTGGAATTTTTTCA[C/T]TTCTGTAACTCTGAG | 114088 |
rs556212979 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053108 | GAGGTTACAGTGAGC[C/T]GAGATTGTGCCACTG | 114088 |
rs556222308 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998712 | TACACTCCAAGCCAC[C/T]GGGGATAGGTTTTCA | 114088 |
rs556253715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091057 | TTCTTTTAACAAGTA[C/T]GTTGAATAAAGGAAT | 114088 |
rs556260993 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050832 | CCATTGGATCTCAGC[C/T]AGCACCAACCACCTT | 114088 |
rs556280412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062581 | GTAGATCTATGTTTA[C/T]AGGGGTTATTTTGGT | 114088 |
rs556287633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083707 | CATCCTGAATGTGAG[A/G]GAGTTGAGATACATA | 114088 |
rs556288658 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012606 | GATCATGTGGCAATG[C/T]TATGTTTAATTTTTT | 114088 |
rs556355445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054923 | CAACCTCTGCCTCCT[A/G]GGTTCAAGTGATTCT | 114088 |
rs556376806 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092377 | AGTTGAGAAAACTTT[C/G]ACTGATTGCTGAAAA | 114088 |
rs556453815 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097035 | TTACACTTTGTATGA[A/G]TTTGAACTCTGCTTA | 114088 |
rs556463931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018320 | TCCTCCCTCCCTTTT[G/T]TCTTTCCTTCTTTCC | 114088 |
rs556495067 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072784 | CTCCCTAAATTGCTT[C/T]ATAATATTTCTAAGT | 114088 |
rs556522337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055531 | GGGAAGCAGAAGAGA[A/G]TCAGGAGGGGATGTG | 114088 |
rs556527453 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019606 | ATTATGGTATCATAG[A/G]AAACAAGCCCCTGGA | 114088 |
rs556544902 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998256 | CGAGGGAGGCAGTGT[C/T]GCTCAGTGGTTAGGA | 114088 |
rs556547589 | in-del | -/AGAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988719 | TTCAAATGAATTACA[-/AGAG]AGAAACACTTTCCAA | 114088 |
rs556567579 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981534 | TTGTTTTCTTATAAT[A/G]GATATCCATTGGGAT | 114088 |
rs556608054 | in-del | -/TT | 0.403161 | 0.19759 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072660 | CAATTTATTACTTTT[-/TT]TTTTTTTACTTAGAG | 114088 |
rs556634135 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978423 | GGTCCCCCTTCCAGG[C/G]CCCAGCCCAAGAGTC | 114088 |
rs556637542 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979711 | ATTTTAATACCGCAG[A/G]TATACTGTATACCTG | 114088 |
rs556647183 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986644 | TGTATTTTTCTATTA[G/T]ATGGATGAGCTGATT | 114088 |
rs556660491 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012973 | TATGATTTTCAAATA[C/T]TTCATACTGTTGGGT | 114088 |
rs556671210 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006086 | CAGAGATGTTTGATA[A/G]AATTCTGAGTCAAGA | 114088 |
rs556675828 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018316 | TCCCTCCTCCCTCCC[-/T]TTTTTCTTTCCTTCT | 114088 |
rs556728225 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983668 | TAAACTCTGTAGCTG[A/T]ATTTTTCATCTTCCA | 114088 |
rs556731895 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072014 | AGGGAAGTAGAAGGC[A/G]GGGAAAGGAAACTTT | 114088 |
rs556754132 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991747 | CCACAAAGGTACTAA[A/T]TGTAAAGACTCAGAG | 114088 |
rs556774157 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051254 | TTGTCTTTGCAAGAA[A/C]GGAAGAGAACAGTGA | 114088 |
rs556797473 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071179 | GTCAGGAGTTCAAAA[A/C]CAGCCCGGACAACAT | 114088 |
rs556801918 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077345 | AGGCGACCATGAGCT[C/G]TCAAACTTAAGTCCT | 114088 |
rs556819117 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078745 | GTGGTTACCATGGTG[C/G]GGAGAAAATGAAGGA | 114088 |
rs556832670 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983350 | ACACCAATCACGTAA[A/G]TAAAAGATAATTACA | 114088 |
rs556884430 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084575 | TTGTTAAAAGCACCA[C/T]AGATTTATCTGTGCC | 114088 |
rs556914662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044914 | TCTTTTAAGAAAGAA[C/T]AATCCAGGCTATCCT | 114088 |
rs556923949 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995021 | CTCCTTTCCTTTTCT[C/T]TGTCTCTTTTTTTTA | 114088 |
rs556942622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986084 | AAAGGACTCATTCTA[C/T]GGAGCGGCAATCTTT | 114088 |
rs556987202 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026778 | AAGGGTGCAGATTCT[C/T]GCTCTATCCCCTATA | 114088 |
rs557113827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035063 | GAACAGATTTCAAGA[C/T]AGCAATAGATATATG | 114088 |
rs557120323 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026976 | CTGGCTGTTCAACCC[G/T]TTATACATTGTTTTA | 114088 |
rs557125521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093226 | TCTTCGTGTCTAGCC[A/G]TGGTGGAAATATCAT | 114088 |
rs557144786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000040 | TACCAGTTCTATCTG[A/G]TGAAAGGCCCAGAAC | 114088 |
rs557149354 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034345 | AAAGAGCAATAAGAA[A/G]TTTTTGAAAAAGGGT | 114088 |
rs557150531 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036854 | TTATCACAGGGAAAT[C/T]TGGGCTATCTACATC | 114088 |
rs557155334 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080999 | TTTGCAGTAGGTCGT[G/T]ATAGGCCAGTCTTGA | 114088 |
rs557232970 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059681 | CACACACCTGCAGTC[C/G]TAGCTACTTGGGAGG | 114088 |
rs557265715 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047812 | CACAACTTTTAAACA[-/C]AAATTTATACTTCAT | 114088 |
rs557272741 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994534 | GTCAGATGTCTAGCC[C/T]CTACCTAAATAGACT | 114088 |
rs557299781 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992972 | TTATCACTGACTACC[A/T]TCTCCCCATTTTCCC | 114088 |
rs557301880 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985483 | TTTACTTTTATTGTA[A/C]TTTGTCAATAAAGAT | 114088 |
rs557313857 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068932 | ATGGAATGAGGTTGA[C/G]AACATGATTTTTAAA | 114088 |
rs557334181 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085026 | CCTCTCTGCAACCTG[C/T]TTTGTTCAGAGACTA | 114088 |
rs557359315 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080630 | GGTTGAGCAAATGAT[C/G]TTCAAGATCCAGTGT | 114088 |
rs557417765 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987865 | AGAATGCAATGCCAC[A/G]ATCTCAGCTCACTGC | 114088 |
rs557418491 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986314 | GGGGCAGGGAGGGAA[C/T]TTTCGGCAGATCAGG | 114088 |
rs557426278 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047168 | CTATGTGGCTTTAAG[C/T]CTCTGGGCCTTTTAA | 114088 |
rs557439221 | snp | A/G | 0.0011611 | 0.0240666 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985990 | TAAAGAGGAATGCAA[A/G]CTCAGCTGGTGGGGT | 114088 |
rs557441672 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071332 | GCTGAGCCGAGACTG[C/T]GCCATTGTATTCCAG | 114088 |
rs557469291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073830 | TTTTTTGCAGCTGCA[A/G]GCTTACATCATTTTA | 114088 |
rs557474047 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044536 | TTTTATTCTTTCTGC[C/G]CTCTGAGTCATGGCC | 114088 |
rs557475738 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015608 | AGCCTCAACCTCCTG[G/T]GCTCAAGTGATCTTC | 114088 |
rs557476062 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048161 | CCCCCAACTATCTGA[A/G]AGTGCAGAGGTTTTC | 114088 |
rs557476368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068691 | ACTATGGGTGGGTTA[C/T]GAGTTGAGAAGAATA | 114088 |
rs557551202 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028097 | AATCATTCCTAGTAG[C/T]AGACAAAGAGTTTTG | 114088 |
rs557629325 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998955 | TACTAAGAAGACCAC[C/G]GTCTTGGATCACCCA | 114088 |
rs557629834 | snp | A/G | 0.000232248 | 0.0107736 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094754 | CTTGTCCAGGTCCAG[A/G]TAGTCATAGTCGGAG | 114088 |
rs557709337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078663 | ACAACGATATTGTAT[A/G]ATATTTTAAAGTATT | 114088 |
rs557767250 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031451 | AGAGGGTAGGGGTCT[A/C]ACTTCAATAAGCACA | 114088 |
rs557878562 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070329 | AAACATACATAAAAC[A/T]AGTTTATGCATTGAT | 114088 |
rs557924920 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050687 | CTTCTGAAGCCAGGT[C/T]ATAACAAGAATACAG | 114088 |
rs557928424 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032247 | AACAGGATAGACTTC[A/C]AAGTCAGATGAACTT | 114088 |
rs557970149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001163 | TGTTTTACATGGAGG[C/T]TGGGGTTCCAGTCCA | 114088 |
rs558008321 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012951 | GATATCAGTCTCTTA[A/T]CAGATATATGATTTT | 114088 |
rs558051801 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038062 | TCCATGCCCGAATCC[C/T]CAGAACCGGTGATTT | 114088 |
rs558075127 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001829 | CACTAGGTCAAGTCT[A/T]CTCATTTTCAGGTAT | 114088 |
rs558076730 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014038 | AGGTACTGGAAGTCC[A/G]AATAATAAGGACAGA | 114088 |
rs558174829 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059915 | TCTTTAGAATATTGG[C/T]TACTACCACGGCCCT | 114088 |
rs558178493 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089167 | GAGTTGATTTTATTT[C/T]ACTTCCCATGAAATC | 114088 |
rs558203139 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021030 | TTTAGCGGGGAAAAC[C/T]GTTCAGTTTCATTTC | 114088 |
rs558214188 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021296 | CCCTGACAGCTTTGC[C/T]GATTCCTGCAGGTAG | 114088 |
rs558239979 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023329 | ATGAGGAGGGAGTGG[G/T]GCATTGCTGAGGCAC | 114088 |
rs558274608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086698 | CAGATATGGACGCTA[C/T]GGAGGAGGGTGAGCT | 114088 |
rs558278757 | snp | A/C | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079640 | CTAAAGCTGCTACAC[A/C]TGAGGTATAATTCAA | 114088 |
rs558313298 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086084 | TGACTCAATTTCTCA[A/G]TAATTTTCATATACG | 114088 |
rs558337791 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020679 | GACATCTGCAGCCAC[A/G]GCACAGTCCTTAACT | 114088 |
rs558372570 | snp | C/T | 0.00138609 | 0.0262892 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979286 | TTGGTCTGGGCCTTA[C/T]GCTGTCAGCTTCCCT | 114088 |
rs558400142 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028124 | TTTGGCCCCATCTAG[A/T]CCCAGGATTTTATAT | 114088 |
rs558462542 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981084 | CTCTGCCTAGGAAAT[C/T]TGTGAAAAATACATT | 114088 |
rs558501275 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075861 | ACTGAATGCAAAAAA[A/T]TCGTTGTGGGCTCTC | 114088 |
rs558511650 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058923 | AGAATTCTCATGTAA[C/T]GTTTTGCATTTTTCT | 114088 |
rs558522034 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090935 | CCAGGAATTCAAGGA[C/T]AATATCAGGATTTAG | 114088 |
rs558536047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075166 | AGGAGTTAAGTGGGT[C/T]GCCCAAGGAGGTAGG | 114088 |
rs558551335 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027247 | CTCCCAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG | 114088 |
rs558563312 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974767 | AGCACTTTGGGAGGC[C/T]GAGACGGGTGGATCA | 114088 |
rs558593235 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077940 | TGGGCATATAAAAGC[A/G]TTTTGGTTATGCAAT | 114088 |
rs558594042 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096474 | CAAGTTCTAGAAATA[-/T]TCCAATTTTCCACCT | 114088 |
rs558607649 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034275 | CTCTATGTGCCAGGA[C/T]CACTTCTAAGTGCTT | 114088 |
rs558615229 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078266 | TGCCACTGATAAATA[C/T]GATTTAATATCTAAA | 114088 |
rs558669266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009498 | ACAAATCTGAATATA[C/T]GATCATGCTATTTAT | 114088 |
rs558744375 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51087968 | TCATGCCTAAAATCA[C/T]TTTTTGAGTTATTTA | 114088 |
rs558751647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024171 | GAAACCTTCTCCTTG[G/T]AAGCTCTGTCACTGA | 114088 |
rs558753771 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046840 | GTGAGGATTAACTGG[C/T]TCAATATATGTACAA | 114088 |
rs558758679 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054069 | CTGTCACAGAATTAA[A/T]CTTTCTTTAGAAATC | 114088 |
rs558764272 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068809 | ACTCTAGAGCAACTG[C/T]TCTACTGCCATGATG | 114088 |
rs558794463 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080504 | AACTAAAAAATGAGT[C/T]TTTGGATGTTCAGAA | 114088 |
rs558822324 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986913 | GGCCTGAAGATAATT[A/G]TTATATCAGACTAAA | 114088 |
rs558858815 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072421 | TGGATTAACAGACTG[C/T]ATCCAGGTATCTAAA | 114088 |
rs558887499 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081240 | TAGCCAATAAGCACA[C/T]GAAAAGATTCTCAAC | 114088 |
rs558900234 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980625 | GTCATTATTCACTCC[C/T]GCACTTCAAAACAAA | 114088 |
rs558924298 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082771 | GGTATGTGAGTTACA[C/T]CTCAAAAAAAAAGTG | 114088 |
rs558936364 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080809 | TCCAAAGCCAGAAGT[A/G]GAAGTTGGGTAAGGA | 114088 |
rs558975213 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085722 | TTTTTATTTTTAAAA[C/T]CTACTTATTAGTTTA | 114088 |
rs558975445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094048 | TGTGCGCAAGAGACG[A/G]GGACCGTCTGCTGCA | 114088 |
rs559011482 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976144 | TGTCAATTTTTAAGG[C/T]GTGGTATCATAGCAG | 114088 |
rs559017492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088833 | TTTATGGCATCAGAA[C/T]GCAGCCTTCTAAACA | 114088 |
rs559069495 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995476 | TTCGAAGAAAAAACC[A/C]ATCAAAATTTATAGT | 114088 |
rs559084731 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072256 | AGTCTTAATACTTTA[A/T]CTTATTATTTTACTA | 114088 |
rs559102532 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041008 | AGGATTCAGTACTTA[C/T]AGGTCAATTTCCTTC | 114088 |
rs559116984 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075020 | ATTTTTATCCAAAGA[G/T]ACTCTTGTCAGGAAC | 114088 |
rs559124446 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029263 | TCAAAAGGGTCACTC[A/G]AAGAGTTGGTACAAA | 114088 |
rs559139108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047990 | TCCCCTTACCAAATC[C/T]GTTAAGTGCATAGTA | 114088 |
rs559170007 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007936 | GCCCTAAGACTTACC[A/G]CCTTATATAATCTCT | 114088 |
rs559222237 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061121 | TGTCATTTTAAAAAA[C/T]TGGATTGTTGGCTGG | 114088 |
rs559238281 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986237 | TTAACAATGCATTCA[A/T]ACAAAGCCTCATCTT | 114088 |
rs559250057 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053317 | AAAATGAGTTTTATT[C/T]TAGGTCCTCCCACAG | 114088 |
rs559256029 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051604 | CAGAGGAGTATAATG[C/G]AATTAGCTATTAATA | 114088 |
rs559258950 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040830 | TTAAATGACCCTTAA[C/T]TCTTCCGCTTACTAC | 114088 |
rs559265772 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035075 | AGATAGCAATAGATA[C/T]ATGACATGACAAATT | 114088 |
rs559295805 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033296 | TGGGGTTTCACCATA[C/T]TGGTCAGGCTGGTCT | 114088 |
rs559303409 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059647 | TACTAAAAATACAAA[A/C]ATTAGCCGGGCGTGG | 114088 |
rs559318223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021802 | GCACCAATGGGGTGA[C/T]AGATGGAATATCAGA | 114088 |
rs559334514 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035325 | AAAGCCTTATTGACT[A/G]TATAGATCTAAGTGG | 114088 |
rs559354104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987946 | GCAGGGACTACAGGC[A/G]TGAGCCATCACGCCC | 114088 |
rs559390361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015541 | TTTTTTTTAGATAGG[G/T]TCTCCCTCTGTCACC | 114088 |
rs559391988 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022748 | CTCTCCTCCTGTCCA[C/T]GGGAAGGAATTCTCC | 114088 |
rs559436764 | snp | C/G | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038575 | CAAAACGACCACAAA[C/G]AATATAAAGAATCTG | 114088 |
rs559495816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026365 | CACCACTAGCTTTCT[C/T]GTTATGTGATAAAAA | 114088 |
rs559507443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046099 | AGGCTTTGGAATGAC[C/T]GCGTTTTAGAAATGG | 114088 |
rs559518907 | in-del | -/AA | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042114 | CCCTCTGCAAAATGC[-/AA]AGTTGATAGCTAAAT | 114088 |
rs559541224 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993409 | GTTTCACTTTTGTTG[C/T]CCAGGCTGGAGTGGA | 114088 |
rs559586193 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056888 | TGTTTCCAGCTTCTG[A/G]AATCATGAGGCAGAT | 114088 |
rs559597016 | snp | A/C/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974863 | AAAAATTAGCTGGGC[A/C/G]TGGTGGTGTGTGCCT | 114088 |
rs559612973 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987205 | TTCTGTGACCAGAGG[C/G]TATTTCCGTGAATTT | 114088 |
rs559615461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994819 | CATGACCAAGTTTTG[A/G]GGCTTGGGGGCCTTA | 114088 |
rs559648680 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082104 | TTCACATTTGGACTT[C/T]ACAGTGACCAGCTCC | 114088 |
rs559667195 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995245 | CTATAAAAATTTTAT[C/T]TTCCTGCTAATCCCT | 114088 |
rs559703812 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003395 | CCATATTAGTCTTTC[C/T]TTTTTCCTTTGTTCA | 114088 |
rs559711803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034816 | CGCTGTGTTTCTTAA[C/T]AGATTTGTGACTTTG | 114088 |
rs559729165 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980225 | GGCTTCTTCTCTGTA[A/C]AGTGAAATAATTATA | 114088 |
rs559734515 | snp | A/C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998713 | ACACTCCAAGCCACC[A/C/G]GGGATAGGTTTTCAT | 114088 |
rs559745990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041361 | ATTGCTGAAGCTGCC[A/G]CTAACATCACACACC | 114088 |
rs559794012 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080683 | TCTCAACTGTAGTGG[A/G]TGGCCACCTTTTTGA | 114088 |
rs559821101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035280 | GTTCTGCTTTTGAAA[C/T]AAAGAATAAAAAGTC | 114088 |
rs559825738 | in-del | -/TTTGTTT | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070776 | ATTAGAAAAATGGCA[-/TTTGTTT]CAGTGTATTTGTTTC | 114088 |
rs559871055 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024844 | AAAAAGGAAGGCAGG[A/T]AGGAAATGAAGGAAG | 114088 |
rs559872828 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067718 | CACCATTTAGGTCTC[A/C]GTTCAGTGTTCCTTC | 114088 |
rs559927214 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006705 | TATTATACCAAATGG[A/C]CTGTTAGGTTAACTT | 114088 |
rs559995110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073368 | GTTTATAGCTGCACT[A/T]CTCTTAGTAGCTCAA | 114088 |
rs560001024 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033313 | GGTCAGGCTGGTCTT[A/G]AACTCCTGACCTTGT | 114088 |
rs560016312 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046610 | TAATGGAGAATTTTA[A/G]AAATTTCATTCTCAG | 114088 |
rs560029608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079960 | GTGCTAGTGGTAAGA[C/T]GCCAAAAAAGCTAGC | 114088 |
rs560041962 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069607 | GTTTGATTTGTTTCA[C/T]GGCATTGTTGGTGTT | 114088 |
rs560074657 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055717 | TAGCCCAGCAAGACC[C/T]ATGTCAGACTTCTAG | 114088 |
rs560093043 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040369 | TTCTCCTCTGGCTAT[A/G]TTGTCACCTTTTCTT | 114088 |
rs560113991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002782 | CGGTCAATTGTCGTA[C/T]ACTTAAGAAAACACT | 114088 |
rs560124251 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048729 | GTGGCTCACGCCTGT[A/G]ATCCCAGCACTTTGG | 114088 |
rs560166478 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090765 | ACCATGCCCAGCTAA[A/T]TTTTGATTTTTCAGT | 114088 |
rs560205828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089080 | TCGAAGATTTGTTAC[C/T]GGAGCATAGTCCAAC | 114088 |
rs560231774 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009747 | AAAGCTCTTTCATTT[C/G]TTATATTCAATCGCT | 114088 |
rs560247060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049424 | CACATCTACTACAGG[A/G]CTGCCACGATTGCTC | 114088 |
rs560263098 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977677 | AGCCTACTGGCCACA[C/T]CACAGTGACCACTGC | 114088 |
rs560265089 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097374 | ACTTGGTTAAATCCC[G/T]GTAATTACAAGAAGA | 114088 |
rs560287355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061336 | GAGAATCACTTGAAC[C/T]CAGGAGGCGGAGGTT | 114088 |
rs560289239 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984319 | AGGATAATGTGCTGA[C/T]TTAAAAGAATTTTAC | 114088 |
rs560302191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008941 | GTAGGTCACACATTT[A/G]TAAGGATACATTTTC | 114088 |
rs560320245 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003013 | GGAAAGGAAATAAAT[G/T]CATTGTCTTGCTCAC | 114088 |
rs560329931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055016 | TGCATTTTCAGAGAC[A/G]GGTTTCACCATGTTG | 114088 |
rs560340812 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51053030 | CCAGGTGCGGTGGTG[A/G]GCACCTGTAGTCCTA | 114088 |
rs560346863 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096173 | ATAGCTTACAGCATC[A/G]TGTGCCTTTCTGTTT | 114088 |
rs560368241 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095237 | AGCTCTCATTGGCCA[C/T]CAGACCCGTCCGTCT | 114088 |
rs560370585 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997679 | ATCATCTGGGCAAAA[A/C]TGGCACATGATGTGT | 114088 |
rs560394187 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983341 | AAATTGAGCACACCA[A/G]TCACGTAAGTAAAAG | 114088 |
rs560400286 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062104 | GTCCAATAAATAAAT[A/T]ATTTATTTATGATAT | 114088 |
rs560415392 | in-del | -/TTT | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013483 | TCAAATTTGTCCTTC[-/TTT]TTCAAGATTGTTTAT | 114088 |
rs560441630 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088409 | CCTGTTCAGAATGGA[C/G]AGTCTCAAACTTATT | 114088 |
rs560448261 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976456 | CAGAGACCATGCCTG[G/T]CTGTTCACCACTGTG | 114088 |
rs560476026 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095601 | TTCCGCTGCTGGCAG[C/T]CTTCGCAGGCGTCTC | 114088 |
rs560514776 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023560 | TGACCCAACACCTTG[C/G]AGGGGAAAGGCAACT | 114088 |
rs560536598 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064411 | TCAAAAGTGTAACTA[C/T]TCCAATTAAAAGGTA | 114088 |
rs560547526 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976369 | CTTGCCCATTTCCTT[C/T]CTAGTACATATGACC | 114088 |
rs560556518 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982212 | CGTTTTCATGCTGCC[A/T]TGCAGGAAGGAGGCG | 114088 |
rs560572772 | in-del | -/TAA | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001536 | GCCCGGCCGCTGTGC[-/TAA]TAATTTTATCATAAA | 114088 |
rs560657437 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049703 | TGGTGGTGGGTGCCT[A/G]TAATTCTAGCTACTC | 114088 |
rs560712414 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069181 | GTGCATGGATATTTT[C/T]CTTTCTTAGATTGAT | 114088 |
rs560739551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017967 | CTGCAAAATATGCCA[A/G]ATGAAACTCTGAAAG | 114088 |
rs560747475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076082 | GCAAATGCTGGGCAA[C/G]TTTTCAAAGACAATC | 114088 |
rs560801023 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017275 | TGTTATTAATTTACC[C/T]ACACTGGCAAACTAA | 114088 |
rs560871086 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001643 | CATTTCCAATATTCC[A/G]TCATTTTTTTTTAAA | 114088 |
rs560874516 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059986 | TACAAATTGTTTCTT[A/T]AAAAAGTGTTTTATC | 114088 |
rs560877144 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990916 | AGGCTGTTTTCATAA[A/G]TGGTCTTATAAGCAG | 114088 |
rs560889439 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095552 | CCCACCTACCGCGGG[C/T]GAGTGCTGCGCAGCA | 114088 |
rs560928896 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040532 | GGAGTGACTGGAGCC[C/G]TGGAGTGAGGGATTG | 114088 |
rs560980361 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976289 | TGGTGCTATGGCCAG[A/T]ATGTGTGGATTTTTA | 114088 |
rs560988721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008759 | ATATCAATATTTCTG[C/G]ATTCCTTTCTGTACC | 114088 |
rs560993709 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077146 | GGTTCTCCTAACTTA[C/T]GTACAGTGTCAAAAT | 114088 |
rs561002618 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002779 | AGCCGGTCAATTGTC[A/G]TATACTTAAGAAAAC | 114088 |
rs561032182 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078794 | CAACGGAGGAGATAC[A/G]TAGGATAAACAGGCC | 114088 |
rs561037523 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974818 | CATCCTGGCCAACAT[A/G]GTGAAACCCCGTCTC | 114088 |
rs561040913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034090 | CCATGACTTTTCAAA[C/T]TGGTAATCCATGACT | 114088 |
rs561067072 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057316 | AGAATTAAAATGCTG[C/T]TTTTGTCTTCTAAAA | 114088 |
rs561083343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054508 | CTGGAACTCCTGGGC[C/T]CAAGCAATCCGCCTG | 114088 |
rs561084319 | snp | C/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096459 | GACAAAAACTCTTTG[C/G]AAGTTCTAGAAATAT | 114088 |
rs561125597 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51015042 | TTAAAATTTTATCAG[C/T]GGAGCCACCATCTGT | 114088 |
rs561130393 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049697 | TGGGTGTGGTGGTGG[A/G]TGCCTGTAATTCTAG | 114088 |
rs561263811 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008128 | GAAAAGATTAGGGGT[C/T]TCCAGAGATTAGAGT | 114088 |
rs561266781 | in-del | -/A | 0.168021 | 0.236177 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045058 | ATGTGAAAATATGGA[-/A]AAAAAAAATCAAATA | 114088 |
rs561271806 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010841 | GCGATGTTTGCTGGG[C/G]GGTCTGTGGAGGAGC | 114088 |
rs561345238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024601 | TTTTCTCCTTCAGCT[A/G]TAGTGGAGAATTTAT | 114088 |
rs561351192 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063594 | ATATTATGAAATTAG[C/T]CACAAAAAGACATAT | 114088 |
rs561446868 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054975 | GCTGGGACAACAAGC[C/G]CGCGCCACCAGGCCC | 114088 |
rs561465374 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028641 | TAAGGGAGAAAGGTA[C/T]GTTCTAAAGCTGTTT | 114088 |
rs561490204 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043330 | CTGAGACATGCAGCC[A/G]GAGGAAGGAGTTTCC | 114088 |
rs561615989 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012178 | ACCATCCATCTCCAG[-/A]ACTTTTTCATCTTCC | 114088 |
rs561617234 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982185 | CCTGGGCGGGTGAGG[A/G]GCGTTGTGTAGCGTT | 114088 |
rs561624302 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977090 | GTTGGACATGGAAGC[A/G]GAAGCAGGCATGACA | 114088 |
rs561632605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070159 | CACAATCCTTAAATG[C/T]TGTCTAGCATTCCTA | 114088 |
rs561726179 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076820 | CAGCCTACCACCGTC[C/G]TTCCCACTGCAAGAT | 114088 |
rs561739238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045016 | TTTGTCTAAGAGGGC[A/G]GTTGGTTCTCAACTT | 114088 |
rs561838280 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035918 | AGAAAAGCATGCTCC[C/T]TGACAGAGCCTTGTA | 114088 |
rs561863642 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981713 | GATTTCCTGAATGTG[G/T]TCTATGTAATAGGTT | 114088 |
rs561867963 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977877 | CTCAATGGATAGCTA[C/T]GGATAAAACTAGAAC | 114088 |
rs561890091 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049400 | CTTGCCTTACCTAAT[C/G]CTTTCAGGCACATCT | 114088 |
rs561919412 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016865 | TCAATCCATTGTTGG[C/T]TGAATTCATGGATGC | 114088 |
rs561951492 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083919 | CTATATGATTCTAGG[C/T]CATCACTCAACCCCT | 114088 |
rs561955718 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019214 | CCTGGAGGTCCAGTG[C/T]GCTCTGCTCACTGTT | 114088 |
rs561981612 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036496 | TACCAGCTCAACCAG[A/T]AACAGAAACTAAGAA | 114088 |
rs562006932 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977954 | TATCAATAGATAATC[A/G]GAAGGTCCTGAAAAC | 114088 |
rs562062298 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031021 | GGCATGGTGGCGGGC[A/G]CCTGTAACTCCAGCT | 114088 |
rs562080256 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059374 | CCATCCCTTAAAATA[C/T]ACAGATGATAGGGTA | 114088 |
rs562087051 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999194 | TTGAGTAGAGGAAAA[A/T]GTCAAGACAAAATAA | 114088 |
rs562123308 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051207 | GATAACTATAGGAAA[C/G]CTTCGTTGTTCCTGA | 114088 |
rs562141743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035840 | AAGGCATATTTTTGA[A/T]CCTCAGTTGTAAATA | 114088 |
rs562158780 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992507 | GAGCCCAGGAGGTCA[A/C]GGTTACAGTGAGCCA | 114088 |
rs562186006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055851 | GAACCCATGAATACA[A/G]TATAACTTGCACAAA | 114088 |
rs562235066 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084720 | TATTAGTTTTATGAA[A/T]TGATGCACTTCATGA | 114088 |
rs562257554 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029432 | GCCAAAGCCCACTCC[C/T]GCTCCTTCCCAGGTA | 114088 |
rs562260827 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056756 | GGCCCAATATCTTGA[C/T]ATTTCTGTCTGACAG | 114088 |
rs562286328 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073028 | TGGAAAAGTGGGTAA[A/G]TGACTTAGCAGACAC | 114088 |
rs562347231 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010780 | CAACGAACACCTTCC[A/G]AAGGTCACTTTGCCC | 114088 |
rs562355441 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025935 | TGCCCTAGCACATTT[G/T]TGTCCTCTCCTCACT | 114088 |
rs562356989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989894 | TAGATAAGGGCAGAG[A/G]CCTCTGCTTAAAAAA | 114088 |
rs562396303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024501 | AGGCCAGAACTAAGG[C/T]TATTTCTGTGAGGCA | 114088 |
rs562402488 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070431 | AGTATTCATTAATTC[A/C]GTGTACTTGGTGACT | 114088 |
rs562473443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082853 | GTGACCAAAGCTATA[C/T]GTAGGTTCTCTTCTG | 114088 |
rs562485227 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028471 | TTGACTGATTTTGTT[C/T]CCCAGATGCATTTAA | 114088 |
rs562503240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050406 | GCCTCTTTGCCTGCC[A/G]CCATGTAAGACATGC | 114088 |
rs562506516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048750 | AGCACTTTGGAAGGC[C/T]GAGGCAGGCGGATCA | 114088 |
rs562525447 | in-del | -/T | 0.303187 | 0.244277 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978766 | TTATCTGTTTTTTTG[-/T]TTTTTTTTTTTCACT | 114088 |
rs562591041 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049831 | CTCTGTCTCAAAAAA[A/T]AAAATAAAATAAAAT | 114088 |
rs562617746 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996641 | GCAAGGGCCTTCTGC[A/G]TTGCATCTAGGAAAG | 114088 |
rs562672775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089145 | TTTATAGTTCCATTC[C/T]CCTTGTGAGTTGATT | 114088 |
rs562695488 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055102 | GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCC | 114088 |
rs562700897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043871 | TAGAAAGCTTAAAGC[C/T]CAAGAGGCCAAATAC | 114088 |
rs562733767 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025128 | ATCTCTATGTGTTTG[A/T]ATGTAAAGAACAACA | 114088 |
rs562764605 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082125 | GACCAGCTCCCATCC[C/T]GAGGGGACCTGGGGG | 114088 |
rs562818539 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991216 | ACAGAGGATTCCAAA[A/G]AATGAAACTGCTTTC | 114088 |
rs562835411 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053510 | TCAGAACAGGTATTC[-/TT]TTTTTTTTTTTTTTT | 114088 |
rs562879397 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998436 | TATATGCAGATTAGC[A/G]TCATGCCTTGTATTT | 114088 |
rs562917559 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046470 | AACTGGGAAAAGTGT[C/T]GAAGGGATTTCTGTA | 114088 |
rs562945044 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014610 | CATTATAGAAATCAG[A/G]CAGATTACCTTAAAT | 114088 |
rs562945372 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999173 | TGCTGGGGGAGGACC[A/G]CACTTTTGAGTAGAG | 114088 |
rs562980515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978803 | TCCCAGACACTTATA[A/G]CTGTGCCTGGCACAT | 114088 |
rs562995301 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51083872 | CAATGGACTTGAGAG[C/T]TAAACAGCGTTCAAG | 114088 |
rs563004470 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067517 | CTTTGCCAGGATGTA[C/T]GTAATTAGACCCCCA | 114088 |
rs563008693 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005316 | TTCAACTTGAGTCAA[A/T]AAAAATAAATACACC | 114088 |
rs563008847 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006389 | AAATAAGAAGATGAA[C/T]GCCACAACAGGAAGA | 114088 |
rs563021295 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044469 | CTGAGAAAGTCCTTT[A/T]AAGGGAACTGATTCA | 114088 |
rs563033841 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089381 | ACTTGTTTAGGTGAG[A/G]AAAGTGCAATTTATC | 114088 |
rs563042381 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068986 | CAGTGATTAGTCTGA[C/T]AGAATATAGAAGAGG | 114088 |
rs563070254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062849 | TCTGCATCTGCCAAG[C/T]GAAGAGGAGTTAGAG | 114088 |
rs563095042 | in-del | -/TGTAAGCAAGAAATTCTAATAAT | 0.0193772 | 0.0965046 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029624 | AGTACAATCAAAAAG[-/TGTAAGCAAGAAATTCTAATAAT]TGTAAGCAAGAAATT | 114088 |
rs563196418 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092694 | ACATCTCCTCAAGAG[A/T]TGCTCCCTTCCTTCT | 114088 |
rs563201007 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011364 | GAATGCCTATATATT[C/T]TTTTATTTCCAAAGA | 114088 |
rs563217515 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049537 | GTAAGTGTAATAATA[C/T]ATAATATAGGCCGGG | 114088 |
rs563234574 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015195 | AGGACTGTTGTGTCT[C/T]TTTGAATTCTCAGAC | 114088 |
rs563239739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978224 | ATGAATTTTGATAAA[C/T]AGTTTCCAAGGCTGG | 114088 |
rs563270238 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081056 | GTCTGCTTTTTTCCT[A/C]CTGTGAGTGTCTGAG | 114088 |
rs563285906 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020005 | CCAGCATTCCTAGTT[G/T]TTTGGATTGCTCAAG | 114088 |
rs563315396 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051915 | GAGGTTGCAGTGAGC[C/T]GAGTTTATGCCACTG | 114088 |
rs563337082 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064266 | ATACTGTAATAAATA[A/T]AAATTGTAACTAAAT | 114088 |
rs563350373 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030131 | GGAGGAGGGAAGAAG[C/G]TTTGGATTCAGGTCC | 114088 |
rs563386701 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051100 | AAGGATCTTAGATTT[A/G]ACTCTAAGCATGATG | 114088 |
rs563389274 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019388 | CAAACCACAGAGTAG[C/T]ATTAACTATAATTTA | 114088 |
rs563422877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013428 | TATTTTGATTATTGT[C/T]GCTTTATAATAAGGT | 114088 |
rs563448674 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030981 | GTGAAACCTTGTCTC[C/T]ACTGAAAATACAAAA | 114088 |
rs563455003 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027262 | GATTCTCCTGCCTCA[A/G]CCTCCCGAATAGCTG | 114088 |
rs563486586 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033135 | CGCTCTGTCGCCCAG[A/G]CTGGAGTGCAGTGGT | 114088 |
rs563512563 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991869 | GGGATACAATAGAGA[C/T]TCAGGTAGGATCAAT | 114088 |
rs563533185 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033236 | TAGCTGGGACTACAG[C/G]TGTGTGCCACCACAC | 114088 |
rs563546124 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999879 | AAGCAGACACATGCC[A/G]GCAGGTGGTGGCACA | 114088 |
rs563569917 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040004 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCC | 114088 |
rs563640213 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073104 | CTTAATACCATTAGT[A/T]ATCACAACACTGTGA | 114088 |
rs563674511 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072424 | ATTAACAGACTGCAT[C/T]CAGGTATCTAAATAT | 114088 |
rs563718226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986331 | TTCGGCAGATCAGGA[C/T]CCAAGACCAGAGGAC | 114088 |
rs563732008 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090162 | GTAAAAATGTTTACA[C/T]GGCACACAGAATGTT | 114088 |
rs563748602 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022347 | TTCCCATGCTCGCCT[A/G]TCCTTCTGCCTTCTG | 114088 |
rs563774813 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984265 | TATTTTCTTTTCTAT[C/T]TAGTAAGGCCTTTAT | 114088 |
rs563846467 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075755 | TCAAAACTTCCCAAG[A/G]CGGGGAGTGGGTCTG | 114088 |
rs563861941 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045983 | AGCAGTTACAACAAA[C/T]GAACCAGTGCAACAC | 114088 |
rs563887086 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983161 | GTGCTTTGCACTGAT[A/G]TAAAAGAAAACTGGG | 114088 |
rs563899167 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991101 | CAAGGACAGATGCAT[A/G]CTTCATCACCAAGTT | 114088 |
rs563900328 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052491 | GTTGTTGCTATTAGC[A/G]TCATTTAATTTATGT | 114088 |
rs563900566 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045193 | GAAATCAGAGACTCC[C/T]TCCCCTGTGAGCATC | 114088 |
rs563900661 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051544 | TTACACAAAGAACCC[A/G]GGAAGAGATGCATTT | 114088 |
rs563987820 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993224 | CTAGGTGACCTGCTC[A/C]CCTGGGATGGGAGGG | 114088 |
rs564010038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038947 | CTTATCATCAGCTAA[C/T]GTCTTCCCCTGAAAT | 114088 |
rs564121350 | in-del | -/AA | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049824 | GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAATAAA | 114088 |
rs564240380 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019226 | GTGTGCTCTGCTCAC[A/T]GTTGGAATACTGCCC | 114088 |
rs564241164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030242 | TCACAGAGTGACTGG[C/T]ACTTGGGGAACCATC | 114088 |
rs564248220 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032571 | CTTGTAGTAGGATTG[A/G]TTGAGGCCATTGCAG | 114088 |
rs564257509 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077016 | AACTCTCATTTTAGC[A/G]CTTGCTATAAAAGGG | 114088 |
rs564329406 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030845 | CTGCTTATTGTTAAT[G/T]GGTTATAAGAAAGAT | 114088 |
rs564330260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998293 | GCCCTGGTGTCATTC[C/T]AATCTGGATTTGAAT | 114088 |
rs564348197 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013038 | ACAACTATTTCCAAC[G/T]TACCTATATTTTCTT | 114088 |
rs564402066 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077580 | TGTATATTTACTAGA[G/T]ATGGGGTTTCGCCAT | 114088 |
rs564436131 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065198 | TGTACATGTGGGCAC[G/T]TGCATATTGCTTCAA | 114088 |
rs564446563 | snp | G/T | 1.65209e-05 | 0.00287405 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981788 | AGGCTTGGTTTGGGG[G/T]CTGCAGGGTACCTGT | 114088 |
rs564447031 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076622 | TCAGAAATTACTAGC[A/G]CCATTTAACATGTGC | 114088 |
rs564492840 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078391 | TAAATAATTTCTCTA[A/C]AAACACTCTTGGATT | 114088 |
rs564522162 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996508 | AGAAATAGTTTTCCC[A/G]CAGATCTGATAACAC | 114088 |
rs564529343 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086153 | GTTTGTAAGTTCATA[A/G]AACTGTGCTTTATAG | 114088 |
rs564529603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992709 | GTCTGCACCATTACA[C/T]CTTTTCTGGGTGGTT | 114088 |
rs564560294 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026805 | TATAAGTGTGACCTT[A/G]AGAAAGTTACCTTTG | 114088 |
rs564569008 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050498 | ACCCCTTTTTCTTTA[A/T]AAATTACCCAGTCTT | 114088 |
rs564569904 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986283 | CACTCAGGCATTTAC[A/G]AAACCAATGTGCCTG | 114088 |
rs564579473 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093380 | TTCCCTAGGAGATGC[A/T]CCTGTCTGGCTTCCA | 114088 |
rs564587622 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052415 | GTAGGAATTCCTCTT[C/G]TCCTGGGAATTAAAT | 114088 |
rs564592480 | in-del | -/ACACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080439 | TGAGTTTTATTGAAC[-/ACACAC]ACACACACACACACA | 114088 |
rs564601330 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072335 | AATCCAGCCATCCAA[C/T]GAGAATTCCTAAACC | 114088 |
rs564603763 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078924 | CAAAAAAGTAACTAA[A/G]TGAGATGATAGACAT | 114088 |
rs564663698 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063760 | TTCAAAAATTAACGG[A/G]AAAGAAAGACATTTT | 114088 |
rs564785825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999778 | GAAGCTCCAAGCATC[A/G]GAACTTCCAGGCAAG | 114088 |
rs564813509 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001408 | CTAATTTTTTGTATT[G/T]TTAGTAGAGACGGGG | 114088 |
rs564873491 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095046 | CAGCGGCGGCGGCTG[C/T]GGTGGTGGTGCCTTC | 114088 |
rs564895963 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074258 | ACTCCGTCTCTACAA[A/G]AAAAAAGTAATGGAA | 114088 |
rs564900418 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066125 | AGGGAGGGAGGGGAG[G/T]GGAGGGGGAGGGAGA | 114088 |
rs564924671 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027200 | CCAGGCTGAAGTGCA[A/G]TGGTGTGATCTTGGC | 114088 |
rs564941150 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073011 | TTTTTTTGGCAACTC[A/C]ATGGAAAAGTGGGTA | 114088 |
rs564971049 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994071 | GGGGGGATTATACTG[A/G]ATTATCCAGGTGGGC | 114088 |
rs564974739 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981624 | CTCTATCATTATATA[C/G]AAAGTAAACCACCAG | 114088 |
rs565006180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009814 | TGGAAGAGATCTACA[A/T]GTTCCTTAACAAAAG | 114088 |
rs565018973 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008538 | CACCCAGAATCTCAA[A/T]GAGACCTTGCCATAT | 114088 |
rs565032018 | snp | C/T | 0.000148259 | 0.00860858 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000800 | GTGGGTACAACATTC[C/T]TCCAGCTGTAGGATA | 114088 |
rs565063621 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021521 | TTGAACTGTAAACTC[C/G]ATAAGGGCAGAAGTC | 114088 |
rs565092179 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076390 | CCTGCTCTGTGAAAG[A/G]CACTGTGTCTTTGGC | 114088 |
rs565095956 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065288 | CGCTGAATGTCAACA[A/G]AGGTGGAAAAACTGG | 114088 |
rs565098441 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975362 | ATTCAGTGTAAACTA[C/T]ATGTTACAAGTCACT | 114088 |
rs565143721 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067800 | CCTTCCAAACACTCT[C/G]CATTACATTCTACCA | 114088 |
rs565156564 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080736 | ATACTGCCATGGTAA[C/T]CCTTAGGAGCCAAAG | 114088 |
rs565196744 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045880 | AGGCATGTTCATGGA[-/T]TTTTTTGTAATGGTG | 114088 |
rs565220609 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054718 | AGCTGGGACTACAGG[C/T]GCATGCCACTACGCC | 114088 |
rs565232853 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069262 | AAGATGAGTCATAAG[A/G]TGCCCTTAAGTGGTT | 114088 |
rs565237452 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988674 | AGCTGTTAACAACAA[A/C]AAAAAAATCCTACCT | 114088 |
rs565237485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981007 | TTTCAGAGACACTAA[C/T]GAGAATGTATCCTGG | 114088 |
rs565273588 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048641 | GGTGTCGTGTAATCA[A/G]TGAAAGGAAGCACCT | 114088 |
rs565340096 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095663 | GCTTTTCTCCTTCTC[A/C]GTGAATCCGCTGACG | 114088 |
rs565346367 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016938 | AAGTTTGAAGTGTTT[C/G]TTCTCCATGCGTCCT | 114088 |
rs565361064 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061199 | AGGTGGATCACCTGC[A/G]GTCAGGAGTTTGAGA | 114088 |
rs565361530 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994920 | AGATGTGCAACTGGC[A/G/T]TTTTTTCCATGGGTG | 114088 |
rs565371930 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040439 | TGGTAACTGCCTACT[C/T]TGGTCTGTGCGCCCT | 114088 |
rs565420011 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992888 | GAATCCCAACCTATT[C/T]GTCATTAGATAAAAC | 114088 |
rs565476446 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033968 | ATCATATACATGTAT[C/G]TGTCCACAAAATAAG | 114088 |
rs565481892 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999950 | GGAGGCCATTCTGTC[C/G]TGCCTTCAGAGGGCA | 114088 |
rs565485870 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992305 | CAAAGGAGCTGGGCA[C/T]GGTGGCTCATGCCTG | 114088 |
rs565517618 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084413 | ATTCACTTCCATAAT[A/G]GCAGAAGGTAGCCGG | 114088 |
rs565528620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022423 | TGCTTTTGGACTTCC[C/T]AGTCTTCAGAACCAT | 114088 |
rs565530466 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007652 | ATAAAATGAGTTATA[C/T]GTAGAACACTTTGGA | 114088 |
rs565549665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063858 | ATTTTTAGTGTCAAG[C/T]GGATTGAAACAAGAT | 114088 |
rs565552636 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006463 | TGAACTCCAGCCAAT[A/C]AAGTTCTATTGTGTC | 114088 |
rs565581320 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051206 | AGATAACTATAGGAA[A/T]CCTTCGTTGTTCCTG | 114088 |
rs565593823 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027905 | CTCTTTTTATTATAA[C/G]CTATGTTTAGTAACC | 114088 |
rs565628326 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029563 | GATCTCTGGGTCACA[C/T]TGCTCAGCAATTACC | 114088 |
rs565632801 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068489 | GCTGCCTGTGTGCCT[A/G]CAACGTGCCAAGTAC | 114088 |
rs565636060 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034324 | GAATTTAGGCCTTAA[C/T]TAGGAAAAGAGCAAT | 114088 |
rs565636710 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037990 | GACTGGGTTCAATCT[C/T]CTGCATGTGAATTCT | 114088 |
rs565670269 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086904 | TATTCATGACTAGAC[A/G]CTCAAAAAAAGTTTT | 114088 |
rs565747059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51056396 | CTATACTACTAAATA[C/G]AAAGGTGAATTTCTA | 114088 |
rs565797677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038521 | ATGCATCTCCTGGTC[C/T]CCTTTTAAGTTGGAG | 114088 |
rs565904400 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994244 | GACCACATCTCTACA[A/G]AAAATTTAAAAAATT | 114088 |
rs565996710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012919 | TGTTGAGTTGTAGGA[C/G]TTCTTTATATATTCT | 114088 |
rs566009867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008194 | CAGGAGGGAGATCTT[C/T]ATTCTGTATCCCGAT | 114088 |
rs566051673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020618 | AAGAGGACATAGTCA[C/T]GCGATGTGGCATCCC | 114088 |
rs566052017 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989340 | CTGCGTTATGCCCAT[-/G]GGATGCAGGAAGAAG | 114088 |
rs566052605 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059623 | ACCAATAGGGTGAAA[C/T]CCCATCTCTACTAAA | 114088 |
rs566076656 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058818 | TGAAGATTATGGATG[A/G]GATTTGTTATAAGCT | 114088 |
rs566100181 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986520 | CCCTTCAGTTGTCCT[A/G]GGAGTTACTACCTAT | 114088 |
rs566120535 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039891 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 114088 |
rs566135282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032672 | TAACTATCTCTCAGA[A/G]TCTGTGTCCAGGGAA | 114088 |
rs566138005 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000564 | GAAGGGCAGGCAGGC[C/T]CTGCCAGGATGGCCT | 114088 |
rs566147766 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002073 | CAGTTCTTCACATAT[A/G]AACTTAATATATGTA | 114088 |
rs566153166 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001473 | TGACCTCGTGATCCG[C/T]CCGCCTCTGCCTCCC | 114088 |
rs566163298 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034295 | TCTAAGTGCTTCACA[A/G]ATAAACCCAATGAGA | 114088 |
rs566183485 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093824 | CCGCGGCCACTGGCT[G/T]CAGACCCGCCGCGGA | 114088 |
rs566197319 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007626 | TTCAACTGTCTACTA[A/G]GGTTATGAGAATAAA | 114088 |
rs566224627 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060397 | CAACCACACAGTATG[C/T]ATTCTGTGTCAGCTG | 114088 |
rs566238739 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979647 | CTTGCAACCTGTTTA[C/G/T]AATCATCACTACCCC | 114088 |
rs566263217 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026873 | AATACTTTGTAGTTG[G/T]GTTATTGTGAGGGTT | 114088 |
rs566279777 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072661 | AATTTATTACTTTTT[C/T]TTTTTTTACTTAGAG | 114088 |
rs566283708 | snp | A/C/G/T | 0.000608319 | 0.0174315 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985907 | CGCGTTTCAGAGATG[A/C/G/T]CTTCAAGGCACAGAG | 114088 |
rs566284578 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087310 | ACCCATGGCCAACAT[C/G]CTGCACTTTAGGCCT | 114088 |
rs566286696 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040179 | ATATTTCCTCGGATG[A/G]TCTTATATTTTCAGT | 114088 |
rs566304380 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981293 | CAAATTGGCATCCAT[A/C]AGCTTTAGTTTAATG | 114088 |
rs566325100 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028096 | CAATCATTCCTAGTA[A/G]TAGACAAAGAGTTTT | 114088 |
rs566344448 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999311 | AAATGACACAGGCAC[C/T]GAAAAGGCAAAGTCA | 114088 |
rs566376832 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51065519 | ATTTCTGAAAAGGGA[C/T]AGGGAAAAATAAAGA | 114088 |
rs566387821 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026595 | GATTCATCTACCCTT[C/T]CCTTTCTGTAAAAGG | 114088 |
rs566420829 | in-del | -/CAAAAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068327 | GTATTTGGTGTGCAC[-/CAAAAA]CAAAAACAAAAACAA | 114088 |
rs566449656 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040622 | AAAGGTTCAAATGCC[A/G/T]TAAAGCTTGTGGTAC | 114088 |
rs566461600 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069887 | TATTTGTGTATTCTG[C/T]ATTTGCAAATTTGCA | 114088 |
rs566504680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027453 | CCAACCAGCTGTTAA[C/T]TCTTATTTGTTTTCT | 114088 |
rs566558621 | snp | A/G | 9.95636e-05 | 0.00705492 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981766 | TGATCAGAAGCCAAC[A/G]TGAAGAAGGCTTGGT | 114088 |
rs566580474 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028702 | TTGGATATTTGTTTT[A/C]TAGGTTACTGAAAAG | 114088 |
rs566596368 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046939 | TAAAGTTTGAAACAG[G/T]TGGTACTAGAATATG | 114088 |
rs566608450 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080853 | CTGCTATATCCAGGG[A/T]CCCTGATAAAGAAAT | 114088 |
rs566609415 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980643 | ACTTCAAAACAAAGA[C/T]GCTAAAAGGGAAAAA | 114088 |
rs566614152 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990072 | TCCAGGCTAGAGTGT[A/G]GTGGTGTTGATCATA | 114088 |
rs566668873 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082322 | TTCATAACAGCATTA[C/T]TAGTAATAGCCAAAA | 114088 |
rs566672882 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989249 | ACAACATTGAGAACA[A/G]TATTGCCACTCCCTG | 114088 |
rs566683713 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047418 | GGTGTGTGGACCCAT[A/G]GGTGACTTTTGAGGA | 114088 |
rs566719237 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073656 | CGCTCTGGACTGGAA[G/T]GGAGCATGCAGGGGG | 114088 |
rs566723593 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018289 | CCTGCCTGCCTGCCT[G/T]CCTTCCTTCCTTCCC | 114088 |
rs566735250 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060794 | CTTATAAGAAGCAGA[A/T]TGATTCTTACATGAT | 114088 |
rs566758492 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987596 | AATGACTTAATATCA[G/T]GTATTATCATTTCTT | 114088 |
rs566758980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995159 | ACCTGACTCCTTTCC[C/T]TTTCTCTTAATAGCA | 114088 |
rs566763146 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996266 | AAGAGAACTTGTTCC[A/G]TTTGTTTCATCTAGA | 114088 |
rs566767264 | in-del | -/TTTTTTTTT | 0.289942 | 0.246789 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027133 | ATGCTGGCTGTTAAC[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 114088 |
rs566778325 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033442 | TACATACATAAATCA[C/T]GAAAACACTTTTGTC | 114088 |
rs566792792 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088790 | TGATTTCTGCTTCAT[G/T]GAATCAAAAACCGCC | 114088 |
rs566804219 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080368 | AGAAAGAAAATGTGA[C/T]TATGGGTGTCTGAGG | 114088 |
rs566822073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994365 | TGAGCTATGATTGTG[C/T]CACTGCACTGCAGCC | 114088 |
rs566832077 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042671 | TTTCCCATCCCTTAC[A/G]TTGAACATCTTCTTC | 114088 |
rs566832169 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035061 | AAGAACAGATTTCAA[C/G]ATAGCAATAGATATA | 114088 |
rs566918125 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041867 | ATATAAAGAATAATG[C/G]CTACTTGTAAGAAAA | 114088 |
rs567002134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980390 | GAGATCTAGCAATAT[C/T]GAACTTCGTCCTCAT | 114088 |
rs567025112 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002441 | GCCCGGCTGGGAACC[A/G]TGTTTTTGCCAGCTG | 114088 |
rs567047618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073538 | GAGCAAGAGAAGCCA[C/T]GCATAAGAGTGCATA | 114088 |
rs567057246 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095845 | ACCGATGGAAATGGT[C/G]AGCATTAGTCAGAAT | 114088 |
rs567065078 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016456 | GTTTCATCCCAGAAC[A/C]ATTCCCCCCCACCCC | 114088 |
rs567082829 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975659 | TACATATATTCCTTT[C/T]TGCCAAAACTTTAAT | 114088 |
rs567118485 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011106 | AAGAAAGAAGACGGA[C/T]GCAGAATTAAGTTTT | 114088 |
rs567121283 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096567 | CCAGAAAAAAAATGG[A/G]CATTTTATTACACTG | 114088 |
rs567135486 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054595 | CTCTTTTTTGTTTTT[G/T]TTTTAGAAGGAGTTT | 114088 |
rs567140070 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010994 | CTCCCCACAGCCCCA[C/T]GGTCAATTGTTCTGC | 114088 |
rs567164460 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080138 | AACTAAACATCAACA[A/T]TTTTTTTTTCTTTTC | 114088 |
rs567173356 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079301 | GCTAGCCTCCAAATT[A/G]AGTAATAATCTCTGA | 114088 |
rs567176908 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040158 | TAACTGTGCAAGAAA[A/T]AGTAAATATTTCCTC | 114088 |
rs567179428 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989948 | AAGATTGGCTGGGGA[C/T]CACTTGTATTATTGA | 114088 |
rs567204558 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010178 | CATGGACCTCTCAGA[C/G]TTGTAGTACATGGTG | 114088 |
rs567260482 | in-del | -/T | 0.0174175 | 0.0916809 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010135 | AAAAGAAGCGAAAAA[-/T]AAAAAGAAAAAGAAA | 114088 |
rs567354121 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033493 | GTTTGGTCAATTACA[A/G]TTATTCAAACAGTGG | 114088 |
rs567389349 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024241 | CGGGCAGAGGCAAGC[C/T]TGGGGCTGCACATTT | 114088 |
rs567391982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027425 | CTGGGATTACAGGTG[C/T]GAGCCACCGTGCCCA | 114088 |
rs567406971 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013893 | ATTCCCCTCTGCTGT[A/T]TGAGGCTGAACTAAC | 114088 |
rs567411105 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086549 | CAACCTTTATCTAAC[G/T]TCTACTAAGTACAGA | 114088 |
rs567436975 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054925 | ACCTCTGCCTCCTGG[A/G]TTCAAGTGATTCTCC | 114088 |
rs567467452 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002382 | CTCATGATCCACCTG[C/T]CTCGGCCTCCCAAAG | 114088 |
rs567471052 | in-del | -/AAA | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068347 | AACAAAAACAAAAAC[-/AAA]AACAAAAAACAAACC | 114088 |
rs567582416 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095337 | AGATCTCTGAAGGGG[C/G]CCGGCGTGCGGAGGC | 114088 |
rs567655145 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027536 | TCCTGGAACAGGGTC[C/T]GTTGGAGAACATTTT | 114088 |
rs567691458 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088705 | CACAATAAAAATAAC[C/T]GAAGAAAATAACCAA | 114088 |
rs567722524 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060285 | TTATATCAGCCTAAC[A/T]TCCTATGACCATTTA | 114088 |
rs567850663 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51059712 | CTGAGGCAGGAGAAT[C/T]GCTTGAACCTGGGAG | 114088 |
rs567865275 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981058 | TGGACCAGGGTCCAC[A/C]GTAGAAATTTCTCTG | 114088 |
rs567880001 | snp | A/T | | | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983409 | GGTGCAGATTGTGTC[A/T]CAAAATTGCATCCTA | 114088 |
rs567929112 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054753 | TAATTTTTGTATTTT[A/T]AGTAGAGACGGTCTT | 114088 |
rs567965924 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061591 | AGAAATTTTTGCTCA[C/T]TCCAAACTGAAAATA | 114088 |
rs567969876 | in-del | -/CCTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018285 | CTGCCTGCCTGCCTG[-/CCTT]CCTTCCTTCCTTCCT | 114088 |
rs567970762 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092752 | TTCTTCCTCATGAGG[C/T]TTATTTCGTTTATGT | 114088 |
rs568082642 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976652 | GGCCTATCCTAATTA[C/T]AGAGCCATCCTAACG | 114088 |
rs568183202 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989055 | ATCTGGGGCCACATG[A/G]AACAGATCACTAGTT | 114088 |
rs568191369 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035008 | GGGTAGTAACATATT[A/T]AGTCATATGGGAAAA | 114088 |
rs568235725 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078083 | GCCAGTGGTCTCATC[A/G]TCAGTATCCTGAACT | 114088 |
rs568252009 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070514 | GACTGGAAGTGTTTC[A/C]GATTTTTTTTTTTTT | 114088 |
rs568258548 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082277 | CAAGGTAATTGAAAA[C/T]ATGTCCACATAAAAA | 114088 |
rs568285933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075060 | GAAACATCAGTAAGT[C/T]TAGATCCCAATTAAA | 114088 |
rs568334284 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016374 | CCTACTGTGAACTGC[A/G]CATGCAAGGGATCTA | 114088 |
rs568356131 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975843 | TTCAAGGGTAACCTA[C/T]GTAAGTCTATCTCTA | 114088 |
rs568365836 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029148 | CTTCACGTGGCCTTT[C/T]CCCCTCAATTCACCA | 114088 |
rs568390702 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075715 | ATTAAAAATGGCAGC[A/G]GGGATGCCTGAGCTG | 114088 |
rs568399160 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068237 | TATGCCAGGACCGTG[A/G]GGATGAAAAAGGAGT | 114088 |
rs568399976 | snp | A/G | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983622 | AAAGCACATCTTTTT[A/G]CCATTTAATAAATCC | 114088 |
rs568406962 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029793 | GAGTGAAGGTTTCAC[C/T]ACTCACATACGGAAC | 114088 |
rs568425231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030585 | GTATGAGTGTGCATA[C/T]GGTGTGTGTGTGTAT | 114088 |
rs568430197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043995 | GATCCAAAGAGAATC[C/T]GATAGACTGGAGCAA | 114088 |
rs568470267 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036830 | AACTTAATCTGACAG[C/T]TTTTCCCCTTATCAC | 114088 |
rs568492266 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982832 | AGTTCTAAATGCCAC[C/T]TATAAATATCACACT | 114088 |
rs568523688 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018832 | GGAATAACTGTAACA[C/T]TTTTTTTCTTTCAGA | 114088 |
rs568525057 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025958 | TCCTCACTAGCCTCC[A/G]ACACCAAGGCTTACT | 114088 |
rs568530765 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980823 | ATAATACACACTTGA[A/G]TGCTATAGAAGCTAT | 114088 |
rs568556914 | in-del | -/AAAAAC | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037422 | ACCTAGACCCCTGAT[-/AAAAAC]AAAAACAAAAACAAA | 114088 |
rs568574127 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994182 | AGGCCAAGGGAGGAG[A/G]ATCACTTGAGGCCAG | 114088 |
rs568619507 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076714 | CATTCCTTTCATCTT[A/C/T]GCAACAGTCCTTGGT | 114088 |
rs568645510 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004386 | TTTTCAAATGTCTTC[C/T]CTTTTTAAGGCCACT | 114088 |
rs568673337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034318 | CAATGAGAATTTAGG[C/T]CTTAACTAGGAAAAG | 114088 |
rs568676709 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51036188 | TGATGAGCCAGCCCA[C/T]GGCACAAAAAAGCCA | 114088 |
rs568727597 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061028 | TTCACATTTTCTTGA[C/T]AAACAATGATGTTGA | 114088 |
rs568765675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51068069 | ATTAAAACACAGGTT[C/G]CTGGACCCCCAAACC | 114088 |
rs568806864 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048856 | GGGTGTGGTGATGGA[C/T]GTCTGTAGTCCCAGC | 114088 |
rs568809214 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090885 | TACAGGCATAATCCA[C/G]TGCACCCAGCCCTGA | 114088 |
rs568812859 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028196 | ATTTCCTCTTTGTGT[G/T]TATGGTCCGTCCCAA | 114088 |
rs568836067 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034945 | GCCTGGGCAGGCTAC[C/T]CTGGCACATAGTAAG | 114088 |
rs568847070 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087949 | TATATTACATTAATA[C/T]TCCTCATGCCTAAAA | 114088 |
rs568923902 | snp | C/T | 6.59435e-05 | 0.00574172 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010404 | AAAAACCACTAGGAT[C/T]ATTTTCCTTAATCAC | 114088 |
rs568955790 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067967 | CTAAAAATTACTGAC[A/G]CATAGCAGGCATTCA | 114088 |
rs568988334 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983074 | CCCAAAAGGACTCAA[C/T]TTAAAATGCCACATA | 114088 |
rs568996734 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51041640 | ATGGTATGAATTTAA[C/T]TTCTCATTATCTATT | 114088 |
rs569037253 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076523 | GTATAGATACACAAT[C/G]ATAGTAAAAACCTGG | 114088 |
rs569054207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088644 | GGAGTAATTTCGAGT[C/T]GGTAAAAAAAAAAAA | 114088 |
rs569061537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048971 | CCTAGGTGACAGCAT[A/G]AGACTCCATCTCAAA | 114088 |
rs569088604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080933 | AATCTAGATGGACTT[C/T]ATCCAAGTTCTGTCT | 114088 |
rs569147377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054667 | CAAGCTCCGCCTCCC[A/G]GGTTCAAGCTATTCT | 114088 |
rs569158829 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989656 | AGAGCTTTGCTGAAT[G/T]AAAGCAGTTTAGCAG | 114088 |
rs569162829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50990188 | GCACCTGGCCAATTT[C/T]AATTTTTTCTGTAGA | 114088 |
rs569164547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075015 | CGGACATTTTTATCC[A/G]AAGAGACTCTTGTCA | 114088 |
rs569203498 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074489 | CTCAAAAGCCCTCTC[C/T]TGCAGAATGAGAAGG | 114088 |
rs569232102 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062640 | AAACCTGAAGATTTA[C/T]TGGCCAGTGGTGAGG | 114088 |
rs569239710 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997791 | CAGCTTCTTCAACTG[C/T]AGCTTATTTAGATTG | 114088 |
rs569244751 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069615 | TGTTTCATGGCATTG[C/T]TGGTGTTTTTAATTT | 114088 |
rs569343945 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001704 | GTAAGTAGCTACAAC[A/G]GTGGATTTTTGAAAA | 114088 |
rs569398777 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029609 | AGTACATTGCTGACA[A/T]AGTACAATCAAAAAG | 114088 |
rs569441211 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025207 | AGAAGGAAACTCTCC[C/T]GCCACACAGTTACGT | 114088 |
rs569442383 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005673 | TTTTTTAATTACTCT[C/G]TAATAAAAGTAGAAG | 114088 |
rs569443458 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046738 | TTCCCATGTATTACC[C/T]GTAAAACCCTGGGCA | 114088 |
rs569496797 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089385 | GTTTAGGTGAGGAAA[C/G]TGCAATTTATCATAC | 114088 |
rs569503301 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044371 | TTCCAAGCAGCAATG[C/T]ACCTGGCTAAAAATA | 114088 |
rs569511559 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077296 | AGTATAGGTGACACA[A/G]TGGCCAAGATAGGGT | 114088 |
rs569530729 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983557 | CAAAGCCCTTTTTAT[A/T]TTATTTAGTTTGTTG | 114088 |
rs569538015 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51091185 | TGGAGTTTTGAAGAC[C/T]AAAAATATCTGAAAA | 114088 |
rs569601817 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003337 | GTCCTTATTAGTTAG[C/T]GCCCACCATGAAACA | 114088 |
rs569710701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057151 | TTCTTATTTTCATCA[C/T]CCTAAAACCCCACAA | 114088 |
rs569719555 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063999 | TATCTAAAAGGCATA[G/T]GATTATTAAAGGCAA | 114088 |
rs569727762 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018352 | TCCTTCTTTCTATCC[C/T]TCCTCCCTCCCCCCT | 114088 |
rs569741459 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015619 | CCTGGGCTCAAGTGA[A/T]CTTCCCATCTCAGCC | 114088 |
rs569745091 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044727 | GTGAAGAATAAATCA[C/T]GAGTTTAAGCCAACC | 114088 |
rs569756340 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062597 | AGGGGTTATTTTGGT[A/G]GGGGAGGGATATCAA | 114088 |
rs569765890 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055242 | ATTCCAATAAGAAAT[A/G]AAAGCACGGCCAATT | 114088 |
rs569800142 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063223 | TAATAAGCATCAATT[C/T]AATGGGCTTAACAAT | 114088 |
rs569805208 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993926 | AATAATACCTTCCTC[A/G]TAAAGTATAGTACTA | 114088 |
rs569826625 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054599 | TTTTTGTTTTTTTTT[A/T]AGAAGGAGTTTCGCT | 114088 |
rs569837031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070367 | CAAAAATTTTGTGAC[C/T]AGAGGCTCACAGGAA | 114088 |
rs569859664 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014302 | GAAGCTTAATTGTTG[C/T]ACTGCCAAAGAGCCG | 114088 |
rs569886302 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080544 | TAAATAATAAAAAAA[A/G]GGGGTCTTGGCAATA | 114088 |
rs569905258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024847 | AAGGAAGGCAGGAAG[A/G]AAATGAAGGAAGAAA | 114088 |
rs569925475 | in-del | -/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063976 | TTGTATAGTTTCCCT[-/C]CTTAATTTATCTAAA | 114088 |
rs569963298 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027396 | TGATCCACCCACCTC[A/G]ACCTCCCAAAGTGCT | 114088 |
rs569997748 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058284 | TTATCTGAACATCCT[C/T]GAGCTAGTTACTCAG | 114088 |
rs570024981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014317 | CACTGCCAAAGAGCC[A/G]GGGAGTTTCAGCAGG | 114088 |
rs570031750 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020339 | GCACTGGTGGCTGTT[C/T]TTGGAAGCAATGACA | 114088 |
rs570033840 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064559 | AGAAATCAATGAAAT[C/T]GAGAATAACAGAAAT | 114088 |
rs570086464 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979187 | ACTAGTCTGCGTCCA[A/G]GTATAAAGAAGGTGC | 114088 |
rs570087902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020123 | GGAAGAACATAAGAT[C/T]ACCCCTGCAGGACAG | 114088 |
rs570117982 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987343 | AATATCATCCTATGT[-/G]AAGAGCTCTGAACAA | 114088 |
rs570137546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038460 | CTTACCACCTTTGGC[A/G]GTGGTCGGATTGCTT | 114088 |
rs570278430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078063 | TCAGTGGTCTTATCA[A/G]ATGAGCCAGTGGTCT | 114088 |
rs570335935 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982478 | TGTAACCCCTGAGGC[A/G]GGGAGGCTAGGAGCT | 114088 |
rs570352470 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074855 | CAGGGCACTTCCAAG[G/T]CATAGGTAAAATGAG | 114088 |
rs570354037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071944 | TGGTGAGGTGCTACG[C/T]ATTTGCCAATCCCGG | 114088 |
rs570404776 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976776 | GCTCTGCAGAGCTAA[C/T]GCTACAGGAGAGGTA | 114088 |
rs570469044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063118 | GGAAAAAATGATCAT[C/T]ATGTATGAACAGATG | 114088 |
rs570470795 | in-del | -/A | 0.201418 | 0.245234 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048984 | ATGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 114088 |
rs570473381 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055486 | CAGAGACTATCAAAA[C/T]GTAATCACAAGTCTC | 114088 |
rs570504448 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976714 | TATTTTTGTGCTTCA[A/G]TGAGTAGTAAAACTT | 114088 |
rs570545334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031161 | CCAAAAAAAAAAAAA[A/G]AAAAGAAAGAAAAGA | 114088 |
rs570608957 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057507 | TTTATATTGTATCTG[A/C]TAAAATAAAAGATAC | 114088 |
rs570626049 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997501 | CTTTGGGTATGAAAC[A/G]GAGGCAGTCTAAGTG | 114088 |
rs570645213 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063909 | AGGAATAAAGACCAT[A/C]TGAAATGGGCATAAA | 114088 |
rs570682585 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065430 | GAGAGTCCAGGAAGT[G/T]CACTGTATGGGGCAG | 114088 |
rs570715695 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977136 | AAAGGGAAAAGGGCA[A/G]AGCTGTGGGTGTAAA | 114088 |
rs570742177 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024697 | TGCCAGGGGATCATG[A/G]TTGAAAAATATTTAA | 114088 |
rs570755750 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069554 | AGAAACTGCAAATCC[A/G]AGGCCCTCGGGACAA | 114088 |
rs570775239 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978333 | GTTAATGAGATGCCC[A/T]GCTCAGGAGGGAAGT | 114088 |
rs570782650 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978181 | GCTAGTTTGCAATCA[A/G]TGTTACTGCACATAC | 114088 |
rs570793930 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061793 | ATTTATCCTACTCAG[C/G]GTTCTGTAAGCTTTT | 114088 |
rs570810892 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51020293 | GAGCGAGCCGTGGAG[G/T]CCTGTATCAGTGGTC | 114088 |
rs570823385 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029599 | CCGGTTACTCAGTAC[A/C/G]TTGCTGACATAGTAC | 114088 |
rs570844758 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071098 | TAAGAAAGTGGAGGC[A/G]GCCAGGCACAGGGCT | 114088 |
rs570853805 | snp | A/C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064468 | CCCAACTATAATTAT[A/C/T]TATAAAAAGTGTATT | 114088 |
rs570874150 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026521 | AGGTACAGAGACAGA[C/T]TCCCTTTCCTGCACT | 114088 |
rs570875659 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51090882 | GATTACAGGCATAAT[C/G]CAGTGCACCCAGCCC | 114088 |
rs570914315 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012961 | TCTTATCAGATATAT[A/G]ATTTTCAAATATTTC | 114088 |
rs570942303 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019545 | TAAAGAATCTCCCAG[G/T]TTCATGGATAATAAC | 114088 |
rs570955151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025813 | AGGGGTAGGTACTGG[C/T]GTGATCCTCTGGGGC | 114088 |
rs570993719 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057646 | AAAAATATTATTGCA[C/T]ATTATAAATTTCAGA | 114088 |
rs571001882 | in-del | -/TTTTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015523 | TTTTTTTTTTTTTTT[-/TTTTTTTTTTT]AGATAGGGTCTCCCT | 114088 |
rs571026323 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998628 | CATGTTTGAAACCAT[A/G]AAAACAGGAAGGTGG | 114088 |
rs571039970 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51079150 | AAAGCCTTCATAATA[C/T]GCAAATTAAATAATG | 114088 |
rs571073655 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044108 | AAAAATTTAAAAAAT[G/T]TGCACAAGTACTAGA | 114088 |
rs571089354 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077289 | GTGAGACAGTATAGG[G/T]GACACAGTGGCCAAG | 114088 |
rs571104461 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999277 | AAAAAAGATAATAAA[A/G]GGAAAAGAAAGGCCC | 114088 |
rs571111471 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029162 | TTCCCCTCAATTCAC[C/T]ACAAATATTGGATAG | 114088 |
rs571167456 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085059 | AATGCCTTAGACTGA[C/T]AGACAGCGCAGGCCA | 114088 |
rs571194401 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051662 | AGCTATACCATGGGA[C/T]ACCCAAAGAAAAAGA | 114088 |
rs571201676 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991682 | GGTATCTAATGCTGC[A/T]TCATAGCATTTTCTG | 114088 |
rs571221878 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993008 | GTTAGGACAGGCAGG[A/G]CTGGAAAGCTTCTGT | 114088 |
rs571294586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008267 | TGGAACTATACACAC[A/G]CACACTGTTAAGTGT | 114088 |
rs571295662 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993451 | TCAGCTCACCGCAAC[C/T]TCTGCCTCCCAGGTT | 114088 |
rs571312821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072747 | CTATTTGCATTCGTA[C/T]TGTTTGCACTTAAGA | 114088 |
rs571354633 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092376 | GAGTTGAGAAAACTT[A/T]CACTGATTGCTGAAA | 114088 |
rs571370097 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001849 | TTTTCAGGTATAGAA[C/T]ACCCACTGTGAGCCT | 114088 |
rs571382884 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050167 | TTTCCAAAGATGGCC[A/T]TACCTATGTATTTAT | 114088 |
rs571387512 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032724 | TCAGTTTCCTCATCT[A/G]CAACATGGGGATAAT | 114088 |
rs571393039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051218 | GAAACCTTCGTTGTT[C/T]CTGAAAATTTCCTAT | 114088 |
rs571438242 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009059 | ATGTTGCTCTCTGAC[C/T]TGGGGGATGCAAGGA | 114088 |
rs571482467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999998 | GGGATAGGGCTCCCT[C/T]ACCTTGGGAAGGTAG | 114088 |
rs571486163 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053528 | TTTTTTTTTTTTTTT[-/TT]ATGCGTTAACATTAC | 114088 |
rs571520292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979681 | ACCGTTTCCCTAATC[A/G]TCCCTTGCACATAAA | 114088 |
rs571520351 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50987271 | CTGGACATACACTTC[C/T]ATCAAAATGTTACTC | 114088 |
rs571533179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007178 | TCATTTTTTCCTCTT[C/T]CACCAAAAGCCTTTC | 114088 |
rs571631366 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044562 | TGGCCTTAACGACTG[C/G]AACTCAAGCAGCCAT | 114088 |
rs571635814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047738 | TGAAGAGGTGCCAAC[C/T]CAATGCTATGGGCAA | 114088 |
rs571695239 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095333 | TGCAAGATCTCTGAA[A/G]GGGGCCGGCGTGCGG | 114088 |
rs571709257 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052609 | TTCAATGATATGAGC[C/T]TCTGATTTAAAGTAG | 114088 |
rs571716219 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066584 | TCATGTATATGAACT[A/G]TTAAAAGACAAAATT | 114088 |
rs571736561 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981200 | CTCAAGGAGATTACT[G/T]TATTTCCTTTCCTTA | 114088 |
rs571738137 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001251 | TTTTTTTTTTTTGAG[A/T]TGGAGTGTCGCTCTG | 114088 |
rs571767766 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046904 | CAGGAAAACCGTTGG[C/T]TCTTATTATATGAAC | 114088 |
rs571789221 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021304 | GCTTTGCCGATTCCT[G/T]CAGGTAGGAATGTAA | 114088 |
rs571847234 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027381 | ACTCCTGACCTCAGG[G/T]GATCCACCCACCTCG | 114088 |
rs571849781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026963 | ATGCTGCCAGTTACT[A/G]GCTGTTCAACCCTTT | 114088 |
rs571860755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022019 | GTGTATGGCCACCCT[A/G]TCCAAAATTTCCACC | 114088 |
rs571904044 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033342 | GTGATCTACCTGCCT[C/T]GGCCTCCCAAAGTGC | 114088 |
rs571974762 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030802 | TATCAGAGGAATCTT[A/T]TGGGTAGGGATTTGC | 114088 |
rs571990774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077525 | AGACTCTCCAAGTAG[C/T]TGGGACTACAGGCCC | 114088 |
rs572032042 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985398 | GAGCACAGGCTTTTG[C/T]AGAAAATGCTTTCAC | 114088 |
rs572065098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031329 | TTCCTAAGATGACCC[C/T]AGCCTCCCTTAAGGT | 114088 |
rs572067685 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014694 | TTACTTGCTATCTTC[C/T]TCAACTTGCGTTACT | 114088 |
rs572117004 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037185 | TGGAAATTAAGAAGC[A/G]CCATTCTAAATAACT | 114088 |
rs572119559 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050273 | TTGTGGGAGGGACCT[A/C/G]GTGGGAGATAATTGA | 114088 |
rs572128950 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51071318 | GAGGTGGAGGTTGTG[C/G]TGAGCCGAGACTGCG | 114088 |
rs572129590 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001385 | CAGGCGCCCGCCACC[A/G]CGCCCGGCTAATTTT | 114088 |
rs572153974 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984089 | TCTCCCTTCCTTAAG[A/G]TTTGGATACCTGTAC | 114088 |
rs572183923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074973 | GAATTTAAAGTGTCT[C/T]TTCACAAAGGCACAA | 114088 |
rs572191694 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038749 | ACAGCCCCTCCTGCC[A/G]ATCACCAAGAGTGAA | 114088 |
rs572287093 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005207 | TCCATCCCCGCTAAC[C/G]CTCTGGCAGCTTTCC | 114088 |
rs572337866 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025041 | AAGACAGGAACCAGT[C/T]GGAAAATCAGGCTGT | 114088 |
rs572356075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051328 | AGAGCAAGGAAGGAA[A/G]AGATGAGACAAAGAA | 114088 |
rs572358819 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054640 | GTTGGAGTGCAGTGG[-/C]GCGACTCACTGCAAG | 114088 |
rs572361506 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013965 | ATTGGTGCTGCCAGG[A/T]AGCAGACACCTCCAC | 114088 |
rs572383558 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054997 | ACCAGGCCCAGCTAA[C/T]TTTTGCATTTTCAGA | 114088 |
rs572422454 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013255 | TTTGCATGTGGATAT[C/T]CAATTTTCCCCACAC | 114088 |
rs572464013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093347 | AAGTGGGTGTGTGTA[C/T]AGTTGGGAGGAGAAG | 114088 |
rs572473660 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078819 | CAGGCCTGGAGATCG[A/G]ATGTATAACATGAGG | 114088 |
rs572502549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51092492 | TTCTAGTCTCCAAGG[A/T]ATTCTGGGAGACTCT | 114088 |
rs572503246 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075160 | GTGCAGAGGAGTTAA[C/G]TGGGTCGCCCAAGGA | 114088 |
rs572525197 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066794 | TTGCAGCTCGGCGTT[C/T]GCCTTATTTGGACAC | 114088 |
rs572545753 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993160 | CCCGGGCAAATCTCG[A/T]CACTGCCAGCCAAGA | 114088 |
rs572574224 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094949 | CTCCATGGGGACCGG[C/T]CTGGGAGGAGACAGC | 114088 |
rs572594923 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026114 | CCTGACGGACGACAC[C/G]TAAGTGGAAGTCTGC | 114088 |
rs572684891 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070517 | GGAAGTGTTTCAGAT[-/T]TTTTTTTTTTTTTTG | 114088 |
rs572698092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064003 | TAAAAGGCATATGAT[C/T]ATTAAAGGCAAAAAT | 114088 |
rs572748504 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039509 | GCTTTTAAAAACACT[A/G]TGTTGAGCAAAAGAA | 114088 |
rs572758714 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | TRIM9 | GRCh38.p7 | 14:51066091 | GGAAGGAAGGAAGGA[A/G]GGAGGGAGGGACGGA | 114088 |
rs572762366 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074148 | TAATAGCTGGGTGCG[A/G]TGGCTCACGTCTGTA | 114088 |
rs572794207 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011748 | ATGAGAAAAAGCAAA[C/T]ACTCTTATCATTCTA | 114088 |
rs572816660 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976875 | CTACAACCTCATTGT[C/T]TGACAGAAAGCTTAA | 114088 |
rs572854636 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014906 | GGGACAGGGCAAGTT[A/G]CAGGAAGGACACAAA | 114088 |
rs572856679 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022095 | TTCTTAGCACTTTTT[A/G]CTAATATACTCCATA | 114088 |
rs572908875 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033033 | TCAAAATCTGAAACA[C/T]TACTGGTCCTAATCA | 114088 |
rs572922848 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089513 | CCTGAAACTCCAATT[A/G]ATAGCATCTTTTCAT | 114088 |
rs572976361 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072268 | TTATCTTATTATTTT[A/G]CTACATTAAAAAAAA | 114088 |
rs573038644 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032513 | GCTGGGGCCCCCTTG[C/T]TTCAATTTTGGACAA | 114088 |
rs573086591 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986245 | GCATTCATACAAAGC[C/G]TCATCTTTCCCACAG | 114088 |
rs573099063 | snp | A/G | | | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998126 | CTTGACCCGAGCGTT[A/G]TATGTGCTGTTGAAG | 114088 |
rs573165535 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50995408 | TACCCACAGCCTAGC[A/T]CACAGTGGTCACTTA | 114088 |
rs573262039 | snp | C/T | 0.000198413 | 0.00995826 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022784 | TGTCCATCATGCCCC[C/T]CGGGAGCCTGGCTTG | 114088 |
rs573291215 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51028911 | GCGTGGCTTTCGTCC[G/T]CAGCTTCCACCCTGA | 114088 |
rs573306613 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981535 | TGTTTTCTTATAATG[G/T]ATATCCATTGGGATT | 114088 |
rs573315477 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072854 | TAGAGAGCAATGTAC[C/T]GTGTAGGAGATGATT | 114088 |
rs573319717 | snp | C/T | 0.000404672 | 0.0142187 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979320 | TTCGGTTGGATTGAA[C/T]GGCCCTGGGCAGCCT | 114088 |
rs573320666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034532 | ATTGGATTGACCACT[C/T]AGAAGGGCATTTTGG | 114088 |
rs573332174 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075155 | TAGAGGTGCAGAGGA[G/T]TTAAGTGGGTCGCCC | 114088 |
rs573332918 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51060593 | TGCCTCAGCCTCCCA[A/G]GTAGCTGGAACTACA | 114088 |
rs573347175 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001354 | CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGACTA | 114088 |
rs573360617 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047952 | GCGATACTGTGAGAC[A/C]CTGTCTCAAAAAAAA | 114088 |
rs573368799 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095396 | GGATGATTCATCCTC[A/G]CCCGGCTTACTTCCG | 114088 |
rs573369321 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047337 | TCATCACTCTGACAG[C/T]ATCTGGGCCACGGCA | 114088 |
rs573370410 | snp | A/C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006887 | GCGCAGTCCTAAGTG[A/C/G]CCAAGTGACAGTGCT | 114088 |
rs573419843 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067723 | TTTAGGTCTCAGTTC[A/G]GTGTTCCTTCTCAGA | 114088 |
rs573426927 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51081146 | AATAACTCTTATAAC[C/T]CAATAATAAAAGACA | 114088 |
rs573445610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979733 | GTATACCTGTTGGTA[C/T]TGTGTGTATATCTGT | 114088 |
rs573487854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078235 | TAGGACAGGAAGGAA[C/T]GTAGTGGGTATATTG | 114088 |
rs573507711 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002090 | ACTTAATATATGTAG[C/T]TGGGAACCATGGTTT | 114088 |
rs573524286 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51080725 | GACTTTTTTGAATAC[G/T]GCCATGGTAACCCTT | 114088 |
rs573528034 | in-del | -/GAGGCAGAGAATTGCTTGAACCCAG | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049727 | GCTACTCGGGAGATT[-/GAGGCAGAGAATTGCTTGAACCCAG]GAGGCAGAGGTTGCA | 114088 |
rs573531231 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008486 | AGTTGTTATTTTTCT[C/T]TGAAAGAGTTGTTTT | 114088 |
rs573604532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064939 | AAGCTTAAGGCACAG[A/G]TGATTTTACTGGTGA | 114088 |
rs573664427 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027024 | GAGGAAGAATACTAT[C/T]CTTGGGTTTTGTGGG | 114088 |
rs573700062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014150 | TTCAGTTCAATGATG[A/C]ATTCATGTACTGAAA | 114088 |
rs573709690 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51038640 | GAATTAAGGAACAAG[A/G]ATGGGGTATTCAGTT | 114088 |
rs573715048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058489 | CAGCTAGGTGTGGCC[C/T]TGAAACTGACTTCTG | 114088 |
rs573725716 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026779 | AGGGTGCAGATTCTC[A/G]CTCTATCCCCTATAA | 114088 |
rs573730289 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51085158 | TTACTTCTTAAAGTG[A/C]AGGCTGCAAGCAAAG | 114088 |
rs573786574 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50992414 | GAGACCCTGTCTCTA[C/T]GGAAAAAAAAAAAAG | 114088 |
rs573802582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51021388 | GAGGTACTCTGTGAC[C/T]GTTTTAACTGCAAGT | 114088 |
rs573836134 | snp | C/T | 0.000148843 | 0.0086255 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986099 | CGGAGCGGCAATCTT[C/T]CCGAAGGCACTGGAA | 114088 |
rs573885261 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093773 | TGGGCACTGGCGCGG[C/T]TCTACCCAGCTATGC | 114088 |
rs573898334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993107 | TCATTTGGTAGTATC[A/G]GAGCCTCAGAGATGT | 114088 |
rs573965310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51001331 | GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC | 114088 |
rs573997618 | snp | A/G | 2.17536e-05 | 0.00329792 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094888 | GGATGATGGGCTCCC[A/G]ATAGAAGGAGCCGCA | 114088 |
rs574033332 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:50980841 | CTATAGAAGCTATCC[A/G]AGGGAAAAGGAGGCT | 114088 |
rs574060565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50988554 | CAAGTTTATTTAACA[C/T]CCATACTGTACAACC | 114088 |
rs574077290 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979987 | CACACTTTGTATAAA[C/T]GGTGTGAATTAAATA | 114088 |
rs574079178 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004438 | ATTTTATTTGTTTAA[-/T]TTTTTTTTTCAGTGA | 114088 |
rs574097095 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034418 | AAAAAATGAGATTCC[A/G]TTCTTTGCTTATCAG | 114088 |
rs574144317 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067100 | ATCTTCACCTGTATG[C/T]CTATGAGCACCTCAA | 114088 |
rs574144350 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51074622 | TCTTTGATCCTTCCA[C/T]CCCACCCTGCCCTTT | 114088 |
rs574172011 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989406 | AACTATCACAATATG[C/G]AGAAGGCTTCTCAGC | 114088 |
rs574232326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51073887 | TGGCAGTTCCTCCCA[C/T]AGGATATACAGCCAA | 114088 |
rs574252437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51046584 | GAAAATACTCTTGGT[C/T]TTCTATTCTATAATG | 114088 |
rs574252560 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052691 | TGCTGGCACCATGCA[C/T]GCAGACCTCATTACT | 114088 |
rs574255559 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51040025 | CCTGACCTCCTGATC[C/T]GCCCGCCTCGGTCTC | 114088 |
rs574266071 | in-del | -/T | 0.458733 | 0.137588 | intron-variant | TRIM9 | GRCh38.p7 | 14:51072661 | AATTTATTACTTTTT[-/T]TTTTTTTACTTAGAG | 114088 |
rs574270914 | in-del | -/AC | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51048372 | ATGGTCTAGGAAAAG[-/AC]AGTGAGCATGGTATC | 114088 |
rs574406029 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070699 | GCACTGGGAATAACA[G/T]GGATTGACTGCATGT | 114088 |
rs574455457 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081546 | TAGGCGTCCTGCAAT[A/T]CAATCCTATTCTGAC | 114088 |
rs574468751 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028994 | ACTGACTGTGGAGGA[C/T]GTTTCAGGACCTACT | 114088 |
rs574476973 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096084 | CTCTGTAAATGAATC[A/G]CTGTGTGACTGCGGA | 114088 |
rs574477119 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994747 | TACTCTTTTGCAGAT[A/G]GTTTCAAAGACTGGC | 114088 |
rs574484812 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002262 | GAGTAGCTGGGACTA[C/T]AGGCCCCTGCCACCA | 114088 |
rs574508978 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976886 | TTGTTTGACAGAAAG[C/T]TTAAGAAAAAAAGTT | 114088 |
rs574517259 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069733 | ATGGCACCAAGGCTA[C/G]ACTGGACTATAACTG | 114088 |
rs574517300 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51062043 | TAGATTATTTCTTCT[A/T]AAAGTTCACTGATTC | 114088 |
rs574574329 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075402 | TGTTAGTAACTCGTC[A/G]GTGTACTGGAATCTA | 114088 |
rs574595197 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981470 | GAAGTAACTTGCCCA[A/T]AAGTGCTTTTCTGTT | 114088 |
rs574640351 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975281 | TTCTCTCATAAAAAT[A/C]ATTTATTGGCACATC | 114088 |
rs574657824 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51082408 | TATGCAATACAATAG[A/G]ATATTAGTACAGGAT | 114088 |
rs574698051 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977223 | CCCACCACGGCTGGC[C/T]GAGCTCCTTGCTGTG | 114088 |
rs574701562 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974832 | TGGTGAAACCCCGTC[C/T]CTAATAAAAATACAA | 114088 |
rs574708198 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | TRIM9 | GRCh38.p7 | 14:51067657 | CTATTTCATCTGTTC[G/T]GCTGGCCCTTCCTGC | 114088 |
rs574733626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042831 | TGCTCCTGGCAGTTC[C/T]TCTTATTCCAGATCC | 114088 |
rs574834277 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011734 | CAATCAGGAAATAGA[C/T]GAGAAAAAGCAAATA | 114088 |
rs574867942 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054979 | GGACAACAAGCGCGC[A/G]CCACCAGGCCCAGCT | 114088 |
rs574869376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51017888 | ATTCCATGGGTAGCC[C/T]GGGCACCCTATCCCA | 114088 |
rs574871038 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51055677 | TTGTCTCCTAGAGCA[C/T]TCAGCTCTACTGACA | 114088 |
rs574893078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51052836 | ACTATACGAGCCCCA[C/T]ACCTCATTGCTGCCA | 114088 |
rs574904427 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029056 | AATCCATCCCGCCCA[A/T]TGCCTGACTTGCCCA | 114088 |
rs575000132 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014787 | AGCCAGGCCACCTCA[C/T]TGTTGTCTTTGAATG | 114088 |
rs575007861 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51018404 | CTCATCTGAATCAAA[A/G]GATTATTTGCCTGTC | 114088 |
rs575058541 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51027518 | GGGATTCGCAGGACA[C/G]ATTCCTGGAACAGGG | 114088 |
rs575061825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982713 | AAAACACAGTTTGCG[C/T]GCTACTCCTGAAACT | 114088 |
rs575145385 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033506 | CAATTATTCAAACAG[C/T]GGGGTAGACTGTAGT | 114088 |
rs575218367 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975202 | TCCTGAAGAAACATC[A/G]CTCTGACAAAGGTGA | 114088 |
rs575223754 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088228 | TACTAACTTATTCAC[C/T]AATAACTACCTGAAC | 114088 |
rs575224166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51047991 | CCCCTTACCAAATCC[A/G]TTAAGTGCATAGTAA | 114088 |
rs575232902 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022638 | AAAGTCACCCAACAA[A/T]CATTATTTGGGTAAA | 114088 |
rs575251196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075867 | TGCAAAAAAATCGTT[A/G]TGGGCTCTCTTGCCA | 114088 |
rs575271054 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095977 | CGGCCTCCCAAAGCA[A/C]CTGGCTGAGCTTTTT | 114088 |
rs575289412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51008543 | AGAATCTCAAAGAGA[C/T]CTTGCCATATCCCTT | 114088 |
rs575300887 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998383 | ATGGGATAATAATAT[A/C]CACCTTATGAGGTTG | 114088 |
rs575306244 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024227 | CTGATGAAGAGGCCC[A/G]GGCAGAGGCAAGCCT | 114088 |
rs575378512 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976173 | AGCATCAGCAAATAA[G/T]AATGCTGACATCATT | 114088 |
rs575424642 | snp | A/T | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977093 | GGACATGGAAGCGGA[A/T]GCAGGCATGACAGCG | 114088 |
rs575425422 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009511 | TATGATCATGCTATT[C/T]ATGACAGATTTACTA | 114088 |
rs575484789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51075167 | GGAGTTAAGTGGGTC[A/G]CCCAAGGAGGTAGGC | 114088 |
rs575490904 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026176 | CTTTTCTGCTGATAC[A/G]GAACCACTGTGATTG | 114088 |
rs575680921 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061950 | CATATGATATTATCC[C/T]ACACGTTTCAGACCA | 114088 |
rs575725959 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020854 | TCTCTCCCATATAGA[A/G]AGGCTGGAGTTGCCC | 114088 |
rs575741165 | in-del | -/G | 0.0923359 | 0.194016 | intron-variant | TRIM9 | GRCh38.p7 | 14:51002123 | TGTGTGTGTGTGTGT[-/G]TGTTTTTCTTTTTTT | 114088 |
rs575742984 | snp | C/T | 0 | 0 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029882 | AAAAAAGAGAATTCT[C/T]TCACCCTCACAGGCC | 114088 |
rs575756546 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029004 | GAGGACGTTTCAGGA[C/G]CTACTTCTCACGCTC | 114088 |
rs575779411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51088912 | AGTATTTACATGTGT[C/T]AATTCATATGCTTTT | 114088 |
rs575831997 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51024175 | CCTTCTCCTTGTAAG[A/C]TCTGTCACTGATTTA | 114088 |
rs575860647 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51034707 | AAATAGGAGATTAAT[G/T]AAATAAATTATAGAG | 114088 |
rs575861506 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50989322 | CCTACTTAAGTGCGT[A/C]TTCTGCGTTATGCCC | 114088 |
rs575888896 | in-del | -/A | 0.00199481 | 0.0315187 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049178 | TGATTCTCCTGCCTC[-/A]AGCCTCCTGAGTAGC | 114088 |
rs575946495 | snp | G/T | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975257 | CTAAGAAATTCTAGA[G/T]ACATTTTATTCTCTC | 114088 |
rs575965841 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51003814 | TCCTCCATGTGCTGA[G/T]AATTAGTTTTCCGTT | 114088 |
rs575996061 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050894 | GGATTCTACAACCCT[A/G]CTCAAGCCTTCAGAT | 114088 |
rs576021515 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51035077 | ATAGCAATAGATATA[C/T]GACATGACAAATTTT | 114088 |
rs576024625 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TRIM9 | GRCh38.p7 | 14:50991748 | CACAAAGGTACTAAT[G/T]GTAAAGACTCAGAGG | 114088 |
rs576027306 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043520 | AGCCTATCTGTGGCC[C/G]AGGAAGCTAATTAGT | 114088 |
rs576071492 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51037129 | TTCCCCATCACCTCA[C/G]TACATTCCTCAAAAT | 114088 |
rs576108659 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044927 | AACAATCCAGGCTAT[C/T]CTAACATCAGCCTAA | 114088 |
rs576158443 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077370 | AGTCCTGGCCCTCAG[A/T]CTCATCTCCAATTCT | 114088 |
rs576228137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997540 | AGGAGCAGCCAACAG[A/G]CCCTCTCTAAACAGC | 114088 |
rs576236388 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042940 | TATGTAAATATATAC[A/G]TATACATACATGTCT | 114088 |
rs576248653 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998578 | GTATATAGCCCCTAC[A/T]GAGCTCCTTATCCAT | 114088 |
rs576258608 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089733 | CTGGACCCATGAGGA[A/T]GAGTCTCACTCTTTT | 114088 |
rs576263449 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096893 | ATAATTATATTCAAT[A/G]TAGTATTAATTGAAT | 114088 |
rs576273117 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011610 | TTTTATGGATAATAG[A/C]CAAAAGAGAATCTAA | 114088 |
rs576276775 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030717 | TGTGATTGTATGTGA[C/G]ATATGTCATCAGTGG | 114088 |
rs576276802 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025149 | AAGAACAACAACAAC[A/C]ACAAAATAGGAATTT | 114088 |
rs576301988 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075983 | TTTCACTGCTATATT[C/T]CCAATACCTACAAGA | 114088 |
rs576304247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050016 | ATTTGTAGGCAAGAA[A/G]TTTTGGAAGTAAACG | 114088 |
rs576359368 | in-del | -/TCTATTACAGTGG | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51013369 | ATTTCTGGATTCTAT[-/TCTATTACAGTGG]TCTATATATCTGTCT | 114088 |
rs576360495 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51057544 | GAAAATAATTTTTTG[C/T]CATTCAGCAATTTTC | 114088 |
rs576381332 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049601 | GGGAGGCCGAGAGGG[C/G]TGGATCATGAGGTCA | 114088 |
rs576442999 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51042321 | TGTCCCCTCAGCCTA[G/T]CCTCTGGTGCCAGTC | 114088 |
rs576446172 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51084603 | GCCATGTTAGACTTA[C/G]TAGATTGGATGAATG | 114088 |
rs576498152 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983760 | AAATGTACTTAATTG[C/T]AACGGAGAAATCACT | 114088 |
rs576566273 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50984038 | GGGTGTGGTCTCAGA[G/T]ATACATTGGAATCCC | 114088 |
rs576577961 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999716 | AGGGGTCTCCTCTTC[A/C/G]TCAGTGCAGGAACTG | 114088 |
rs576578654 | in-del | -/ATGCACACCAA | 0.00119737 | 0.0244387 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026705 | TGACTCTCTAAAAAT[-/ATGCACACCAA]ATGCTTGGTTGAGGC | 114088 |
rs576637120 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51012692 | AATGCACAAGGGTTC[C/G]AATTTCTCCACATCC | 114088 |
rs576643918 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51006132 | TAGTTATGATTTTGA[G/T]TCAGAACTTTAAATG | 114088 |
rs576647415 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072079 | GCCCATGCTGTGTGC[A/G]GCAAAAAGGCACACG | 114088 |
rs576652383 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51063966 | ATATAACAGATTGTA[C/T]AGTTTCCCTCCTTAA | 114088 |
rs576669284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51016279 | TGGCCTGTTAGAAAC[C/T]GGGCTGCACAGCAGG | 114088 |
rs576681473 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011096 | TGAAAAGCTGAAGAA[A/G]GAAGACGGATGCAGA | 114088 |
rs576723203 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TRIM9 | GRCh38.p7 | 14:51070778 | TTAGAAAAATGGCAC[A/T]GTGTATTTGTTTCTG | 114088 |
rs576796161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049549 | ATATATAATATAGGC[C/T]GGGCGCAGTGGCTCA | 114088 |
rs576799138 | snp | C/G/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997484 | GGTGCTGACGGCCTC[C/G/T]GCTTTGGGTATGAAA | 114088 |
rs576819412 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51076110 | ATCTCATTGATCCTG[C/G]TCTATAACTATAGGA | 114088 |
rs576832836 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050952 | GCAACCTCACGGGAG[A/G]CTCCAACAGAACCAC | 114088 |
rs576850304 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51043388 | ACAATGAAGGGAAGA[G/T]AAAGGTCAAGAGATA | 114088 |
rs576877775 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082493 | TTAAAAACATTATGC[A/G]AAGTAAAAGAAGACA | 114088 |
rs576881767 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058569 | CCCTCCCGTCATCTG[C/T]TCCCACTGTGGTAGT | 114088 |
rs576889522 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51089648 | GAGAAAAACAGAATA[A/C]TTTTGTTTAATATAT | 114088 |
rs576898584 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997392 | CAAGACTGAAGGGAC[C/T]GGCAAAGATGAAAAT | 114088 |
rs576922014 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083835 | GAAATACATTTTAAC[C/T]AAAATAGTATTTAGT | 114088 |
rs576949715 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035161 | AGGATACACATTAAG[A/G]GTTAATTATCAAGGC | 114088 |
rs576988594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51029823 | CAGCTGGAACACAAA[C/T]CCTCATCTGATGGCA | 114088 |
rs577002630 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083697 | CAGATCTGGGCATCC[C/T]GAATGTGAGGGAGTT | 114088 |
rs577010220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023338 | GAGTGGGGCATTGCT[A/G]AGGCACGAGAAATCA | 114088 |
rs577072135 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096224 | GAGGCGGTGATTCTA[A/G]TGTTAGTCCCTGTAC | 114088 |
rs577098313 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054333 | GCTGAAGTATAGTGG[A/C]TCCATCTTGGCTCAC | 114088 |
rs577116233 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078188 | AACACAGATCTAAAT[C/T]CTTTAACATGGTTGG | 114088 |
rs577120498 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016397 | GGGATCTAGGTTGCC[C/T]GCTCCTTATGAGAAT | 114088 |
rs577128918 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51049718 | GTAATTCTAGCTACT[C/T]GGGAGATTGAGGCAG | 114088 |
rs577131710 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51061153 | CGTGGTGGCTCACGC[C/T]TGTAATCCCAGCACT | 114088 |
rs577192533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977779 | TTAGGGCAAACATTT[C/T]TTTCTGGGGTCGCAT | 114088 |
rs577207829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51054892 | TGGAGTGCAATGGTG[C/T]TATCTTGGCTCACTG | 114088 |
rs577208097 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025647 | CATTGATTAATTAAA[A/C]AATCATTTATTGAAT | 114088 |
rs577215993 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985868 | TCCCCCTCACCACGC[-/A]ACATGAATGGCAAGA | 114088 |
rs577221274 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985484 | TTACTTTTATTGTAC[G/T]TTGTCAATAAAGATC | 114088 |
rs577265134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050396 | GGTTCTCATTGCCTC[C/T]TTGCCTGCCACCATG | 114088 |
rs577284485 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51004813 | TGCATCATACTGCCC[C/T]TCTCCAGTCCGGTGT | 114088 |
rs577285737 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51011854 | TTGTATATGACAATT[C/T]TACCTTCCCTTTCCC | 114088 |
rs577307658 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044632 | CCAAGGATTGTGGAC[C/T]AGGAAGAAGTAACCT | 114088 |
rs577344825 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | TRIM9 | GRCh38.p7 | 14:51069671 | GTCATATCAGAATGA[C/T]GCAAATGTCAGGTTT | 114088 |
rs577365932 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978755 | AAGGCAAGATTTTTA[C/T]CTGTTTTTTTGTTTT | 114088 |
rs577451362 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005053 | CATCTGAGGAAAGTT[A/T]AGACTTTAGCAGAAC | 114088 |
rs577453843 | snp | C/T | 7.06053e-05 | 0.00594118 | missense, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977299 | CACATCCTTAGGCTA[C/T]TGATGCTCTGCTGGA | 114088 |
rs577469854 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51078204 | CTTTAACATGGTTGG[G/T]GAGATAAAAGAACAG | 114088 |
rs577516913 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068705 | ATGAGTTGAGAAGAA[C/T]AAGGATGTAAAGTTA | 114088 |
rs577556779 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51077609 | ATGTTGACCAGGCTT[A/G]TCTCAATCTCCTGTC | 114088 |
rs577655030 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51064837 | AATATCCCATATCTA[C/T]TAAAATATTGAAATC | 114088 |
rs577666997 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51026757 | GTAGAAAGAATATAG[C/G]TTTGAAAGGGTGCAG | 114088 |
rs577668037 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51019918 | AGAACTATTAAATCT[A/G]TTCAAGCAATCAGTG | 114088 |
rs577672761 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51032273 | AACTTGAGTTTCAGT[A/G]GTGGCATTTCACTAG | 114088 |
rs577729262 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51033183 | CAACCTCCACCTCCC[A/G]GGTTCAAGCAATTCT | 114088 |
rs577736415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51044885 | TGTCGGCAGTCATTT[C/T]TGTTTTGTTTTTTTC | 114088 |
rs577757345 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999083 | TCTTGTAAAAATGCA[C/G]TTGCTGATCCAGTAG | 114088 |
rs577761209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51031582 | TCCTATTCCCTCATT[C/T]CCCTTGTAAAGTGCC | 114088 |
rs577770933 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TRIM9 | GRCh38.p7 | 14:51050718 | CTTCTGGCTGGCTTC[C/T]TCTCCCTCACTCTCT | 114088 |
rs577790912 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51014097 | AGTCTGCTTTTGAGA[C/T]AAAATAGACTGAATT | 114088 |
rs577830644 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984314 | TTTGCAGGATAATGT[G/T]CTGACTTAAAAGAAT | 114088 |
rs577866956 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51007853 | AAAATCCATTAAAAG[A/G]CTGAGAGATGTACAC | 114088 |
rs577884744 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:50999542 | AATTGTAGAAGACAA[A/G]GCCCCTGCTCTCAAG | 114088 |
rs577900595 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TRIM9 | GRCh38.p7 | 14:51005965 | AATAGCAGCTGGTCT[C/G]AGTGAAAATACGTAA | 114088 |
rs577911223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51039839 | GCAAGCTCTGCCTCC[C/T]GGGTTCACACCATTC | 114088 |
rs577952155 | snp | C/T | 1.65754e-05 | 0.00287879 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000660 | CTTTGGGTTAACAAG[C/T]ACGTAGTGGGCTGTC | 114088 |
rs577989236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51030905 | TAATCCCAGCACTTC[A/G]GGAGGCCAAGGCGGG | 114088 |
rs578005423 | snp | G/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977423 | ACACAGTGTACCGTG[G/T]GTGTGTCCCTAACTC | 114088 |
rs578018748 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50994456 | TGGAAGATGCTACAT[C/G]TCTGGCTTTGTAGCC | 114088 |
rs578044742 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021274 | ATGTGCTAATCACCC[A/C]CTTCTTCCCTGACAG | 114088 |
rs578056187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50993692 | AGCTACACAGCGCTG[C/T]TTCATTTTGACAAGG | 114088 |
rs578082924 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51086711 | TATGGAGGAGGGTGA[A/G]CTGAACAGGTGACAG | 114088 |
rs578120026 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:50986991 | CTCTGAATTACTAAA[A/T]TTGGTCCTTTCTATT | 114088 |
rs578163048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000235 | CAATGATGGTAATAA[C/T]AATAACTAATAATGA | 114088 |
rs578179990 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51045785 | CATTATTTGTAATAA[A/G]TAATTTTTTTCATTC | 114088 |
rs578204376 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51093424 | CAAACTCCGGTCCTG[A/T]CACTCTAGTCTCAGG | 114088 |
rs578220915 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51058455 | CCCAGAATAAAGACT[C/G]CATTTCTTAGCTCCT | 114088 |
rs578244488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TRIM9 | GRCh38.p7 | 14:51051941 | CACTGCACTCCAGCC[C/T]AGGCAACAGAGACCC | 114088 |
rs745338491 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059625 | CAATAGGGTGAAACC[C/T]CATCTCTACTAAAAA | 114088 |
rs745356053 | snp | A/G | 1.68405e-05 | 0.00290172 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998058 | GCCTTACCCTCAGAC[A/G]TTTGGAGGACCAGGG | 114088 |
rs745358564 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981098 | TTTGTGAAAAATACA[A/T]TTGAGGAACACAATC | 114088 |
rs745379838 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005060 | GGAAAGTTTAGACTT[C/T]AGCAGAACTACAAGC | 114088 |
rs745389325 | snp | A/G | | | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094898 | CTCCCGATAGAAGGA[A/G]CCGCACACGGGGCAT | 114088 |
rs745446378 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096821 | TTCAGGTATGGTTGG[A/G]ACATTAGCTGCACTT | 114088 |
rs745453181 | in-del | -/G | 1.73135e-05 | 0.00294218 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094093 | AGACGCAGGGAGTTA[-/G]GGAGTGGGTTTTCTT | 114088 |
rs745458862 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021589 | CCCCTGCCAGCACTA[C/T]GAGCGTAAGACCAGA | 114088 |
rs745488982 | snp | A/G | 1.78774e-05 | 0.00298971 | intron-variant, downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50977358 | TGCAGCGTGACCTGG[A/G]GAATGAGACTGTGAG | 114088 |
rs745516311 | snp | C/T | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025305 | AGCTGTACCAGAAAC[C/T]CCTTGGCTTCTTTGG | 114088 |
rs745528415 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020745 | TAAGCAGGAGGGCAA[C/T]GGGGCTTCTCATGCC | 114088 |
rs745552295 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089837 | GGGATGAGATTTTTA[C/T]GCAGTAATTGTTGAC | 114088 |
rs745561287 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076920 | TTTCCTGACCCTATA[C/T]TGCCCAATGCCATTT | 114088 |
rs745563419 | snp | C/G | 2.00318e-05 | 0.00316473 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094847 | GTTGCGGGCGCACGC[C/G]TGACACAAATTGTGA | 114088 |
rs745580509 | snp | C/G | 2.79716e-05 | 0.00373966 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979290 | TCTGGGCCTTACGCT[C/G]TCAGCTTCCCTCTCT | 114088 |
rs745589753 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081893 | CCCAGCACCTCCACG[A/T]GTTCTCTAACCTGGA | 114088 |
rs745597881 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052178 | TTAACATCATTATCT[C/G]ACAACATTAAATTAA | 114088 |
rs745638058 | snp | C/G | 0.000298191 | 0.0122068 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981774 | AGCCAACGTGAAGAA[C/G]GCTTGGTTTGGGGGC | 114088 |
rs745647287 | snp | C/T | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975145 | AAACAGGGGAAAGAA[C/T]ACATGCTCTCCAGAG | 114088 |
rs745693594 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083195 | TCTAGTTTTCTAATA[C/T]TTTTTGAAATATGTG | 114088 |
rs745732932 | snp | G/T | 3.30169e-05 | 0.00406293 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025236 | GTATTAACCGGCGGG[G/T]TTCCTTGCGTCCCAG | 114088 |
rs745744884 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061468 | GTAAGGATATACATA[C/T]TGAATTTAAGTCCTC | 114088 |
rs745772303 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003953 | GGGTGTTATGTTATC[A/C]TATTTAACTTCATTA | 114088 |
rs745784957 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030346 | CCTGCAAGAATGGAT[A/C]CCTTCTCCGGTTTCT | 114088 |
rs745856167 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976381 | CTTTCTAGTACATAT[A/G]ACCATTTATAATTAT | 114088 |
rs745878624 | snp | C/G | 1.64914e-05 | 0.00287149 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025359 | GCCTGGGAGAGCTGG[C/G]TCTGCAAAGACAAAG | 114088 |
rs745881595 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087379 | AAGTGAAATGATGTC[A/C]TGATGATTTCCCTGA | 114088 |
rs745907749 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008209 | CATTCTGTATCCCGA[C/T]GCAGTGGTGATTATA | 114088 |
rs745923898 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996388 | AAAATAAACTGAGGC[A/G]CTACATCCTCCTGCA | 114088 |
rs745930622 | snp | G/T | 1.8393e-05 | 0.00303252 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982152 | ACAGACCCAACAAGC[G/T]CAGCACCATAACATA | 114088 |
rs745960163 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979832 | GGAGATATCTGCCCT[C/T]GTGAGTTGCTCTGCT | 114088 |
rs745973071 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056698 | ATTCTTAGGCCATTA[-/T]CCTTACTCCCAGTTT | 114088 |
rs746006664 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047020 | CATAAACTTAAGATA[A/G]AGTCACCTTTGAGGA | 114088 |
rs746028500 | snp | A/C/G | 0.000269949 | 0.0116148 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094318 | CCGGGGGCACCAGGC[A/C/G]GTGCTTGGCTAGGGG | 114088 |
rs746042543 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049773 | GAGGTTGCAGTGAGC[C/T]GAGATTGCACCACTG | 114088 |
rs746050951 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997354 | AGAGATGAACCTTGT[A/G]TGGTGGCTCTCGGTA | 114088 |
rs746064618 | in-del | -/AC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046326 | TTGAACTCTCTCTCA[-/AC]ACACACATGCAAATG | 114088 |
rs746066073 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983906 | CCATTTGTGAATACA[C/T]ACATCTTATTAATAA | 114088 |
rs746156689 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062917 | TTGGAATTTCCAAAA[C/T]CCACCCTAACAAAGT | 114088 |
rs746166614 | snp | C/T | 1.64751e-05 | 0.00287007 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000790 | CGCTGTTGTTGTGGG[C/T]ACAACATTCCTCCAG | 114088 |
rs746197892 | snp | C/T | 1.6504e-05 | 0.00287258 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010462 | GGTCTGGCGCAATTT[C/T]ACTGTGCAGTGAGAG | 114088 |
rs746217230 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059588 | GTGGATCACGAGGTC[A/T]GGAGTTCAAGACCAG | 114088 |
rs746238943 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988342 | TAAATTGTACTTACC[G/T]TTTCTATTCTCAGCA | 114088 |
rs746279485 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027983 | AAGTGAAGCTGCCTG[C/G]TGTCTTGTATTCCAA | 114088 |
rs746290407 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018659 | GATAGCTACAATGGG[C/T]ACACGGAGGCCCTCA | 114088 |
rs746316874 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017014 | ATGATGACCAACTGA[A/T]GCTTTGAATTAACTG | 114088 |
rs746322616 | snp | C/G | 1.65154e-05 | 0.00287358 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022799 | TCGGGAGCCTGGCTT[C/G]TTGGCTTTCTGCTCT | 114088 |
rs746330674 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990669 | TGCCCTCTGTGTCCT[C/G]GTAGAAGTCTGGGTT | 114088 |
rs746342824 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038292 | CTTTAGAGCATCCGG[A/T]AAGGAACTCAGCCCT | 114088 |
rs746351996 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045860 | GAAGCAACAGTATGC[A/G]CAAGGAGGCATGTTC | 114088 |
rs746395938 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018956 | TAAGACAATTTCAGG[G/T]TTATGTCAAATTGTG | 114088 |
rs746543371 | in-del | -/C | 0.00010072 | 0.00709577 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094976 | CAGCGACGGCTGCAG[-/C]GGGTGCCTGAGCTGG | 114088 |
rs746581260 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021756 | TTGCTCTTCCCATGC[A/G]TTCATCCTTCCTCTC | 114088 |
rs746611272 | snp | G/T | 1.64757e-05 | 0.00287012 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979381 | CCTCAGGGGCAGGGT[G/T]CTTACCTGCACGTTC | 114088 |
rs746641773 | in-del | -/TGGG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012891 | GCCCATTTTTAAAAT[-/TGGG]TGTTTTTGTTGTTGA | 114088 |
rs746672021 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050034 | TTGGAAGTAAACGAT[A/G]CAGAGCCGTGAGACA | 114088 |
rs746743177 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091676 | TCCTTCTGTCTTATT[C/T]TTTTTCTTGGCAGTT | 114088 |
rs746788661 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005117 | ACTGTTAAAGATAAC[C/G]CTGAACGCAGGTTTT | 114088 |
rs746793722 | snp | C/T | 1.79284e-05 | 0.00299397 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977278 | AGGCAGCTGGCGCCT[C/T]CACGGCACATCCTTA | 114088 |
rs746812395 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095696 | GTGCCCTGGAGCTCC[C/T]CCATCCCGGGAGTCT | 114088 |
rs746841939 | snp | A/C | 0.00023165 | 0.0107597 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025370 | CTGGCTCTGCAAAGA[A/C]AAAGAAGGAAGCCAT | 114088 |
rs746860195 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004303 | TATTCTCACTGACTT[C/T]CTTGAAGAGGTCTGG | 114088 |
rs746881818 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020873 | CTGGAGTTGCCCTAC[C/T]ATCACCATGTGACTG | 114088 |
rs746889511 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073671 | GGGAGCATGCAGGGG[A/G]CTTCTGGAGGCTGAT | 114088 |
rs746950334 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023537 | CACCCTGCCATAAAA[A/G]TCAGATATGACCCAA | 114088 |
rs746972481 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056410 | CAAAGGTGAATTTCT[-/A]AAAAACAAAACAAAA | 114088 |
rs747018975 | snp | A/C | 1.66421e-05 | 0.00288458 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000642 | CCTCTGACAGAGTCA[A/C]TGCTTTGGGTTAACA | 114088 |
rs747059684 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985283 | TACTCAGATCTTTGG[A/T]CATTAGGCATTAGGA | 114088 |
rs747152531 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037048 | TTGCAAACTGTTACC[A/T]TACTATCTTTCATCC | 114088 |
rs747174269 | snp | C/T | 1.66632e-05 | 0.0028864 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009058 | GATGTTGCTCTCTGA[C/T]TTGGGGGATGCAAGG | 114088 |
rs747194277 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987017 | CTATTTTGTCAAACA[A/T]TAGCTGGTTCTATGC | 114088 |
rs747197307 | snp | C/T | 1.86778e-05 | 0.0030559 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094609 | CCGGTGACAAGTGGG[C/T]GGCCGGTGGCGGCAT | 114088 |
rs747202034 | in-del | -/CAAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036489 | GGGGCTTTACCAGCT[-/CAAC]CAGAAACAGAAACTA | 114088 |
rs747214064 | snp | C/T | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50975251 | TAAAAACTAAGAAAT[C/T]CTAGAGACATTTTAT | 114088 |
rs747246100 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065411 | ATGGATAATGGATGC[C/T]TAAGAGAGTCCAGGA | 114088 |
rs747271073 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052209 | TTATCTCAATATATA[C/T]TTTTCCAAAATCATT | 114088 |
rs747305001 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009180 | TGGAGTGAGTGTGCC[C/T]TTACCCCACTGATCC | 114088 |
rs747306561 | snp | A/G | 1.66313e-05 | 0.00288364 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982083 | AGTGCGCCGAGCCAG[A/G]GTCGAAAGCAAACCA | 114088 |
rs747326306 | snp | C/T | 3.29995e-05 | 0.00406185 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979518 | CGAGGAGGACCCCAA[C/T]TGTGGCCCCTTTTGT | 114088 |
rs747331247 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058330 | CATCTACAGAATGGA[A/C]AAGGTATTTCTGCCT | 114088 |
rs747415513 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029896 | TCTCACCCTCACAGG[C/T]CAAAACAATTGTTTA | 114088 |
rs747448446 | in-del | -/C | 1.91687e-05 | 0.0030958 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977393 | AGAGGCATCGTGCAT[-/C]CCCCCTGTCCCTTTA | 114088 |
rs747492090 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076004 | ACCTACAAGAGTACT[A/G]GAGCACCAATACAAA | 114088 |
rs747503367 | snp | C/T | 0.000120359 | 0.0077566 | intron-variant, splice-acceptor-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982966 | GCTTTTTAATGTCAA[C/T]TGTTGTCATTCCAAG | 114088 |
rs747505328 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047718 | GTAAAAAAGAATATG[A/G]CCAATGAAGAGGTGC | 114088 |
rs747508488 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980703 | AGAATCTATTGACAG[A/C]GAGTTCCACAAAATG | 114088 |
rs747537488 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087856 | TTAATGAAAAACTCA[A/G]TTAGACCAGTCATTT | 114088 |
rs747540905 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019538 | ATGCCACTAAAGAAT[A/C]TCCCAGGTTCATGGA | 114088 |
rs747614517 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092718 | TCCTTCTAAGCAGTG[G/T]GGGCATATTATAAGG | 114088 |
rs747640277 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013508 | TTGTTTATTTACATC[A/G]CCCAATTTTCTGATA | 114088 |
rs747641201 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979473 | GTTGTTCATCGTTGA[C/T]AAAAAATGTCAAGTT | 114088 |
rs747645123 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007005 | CATCCTGCCAACTGG[C/T]CTGGACTCCACCGTG | 114088 |
rs747681905 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091786 | ATGGTCTTCTAGCCT[A/G]CTTATGTCATGTTTC | 114088 |
rs747696000 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008734 | TTTCAATTCTGGACT[C/T]CCCTGATTTATATCA | 114088 |
rs747702558 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989630 | CACACGCAGGGATCC[C/T]GTGTGGTTGCAGAGC | 114088 |
rs747729704 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012120 | TTTCAAGTGTGTAAT[A/T]CCGTGGCATTAAGTA | 114088 |
rs747747688 | snp | C/T | 1.64741e-05 | 0.00286998 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022919 | GATGAGGGCATCACA[C/T]TGGGCCACCAGACAG | 114088 |
rs747752137 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002768 | TGAGAAGGTGAAGCC[A/G]GTCAATTGTCGTATA | 114088 |
rs747787674 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028859 | GTTCAAGCCTGAAGG[A/G]GAGAAACAAAGAACT | 114088 |
rs747809558 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070101 | TCATGTTTTTCATTT[G/T]GGTGCTTTTTGGTGG | 114088 |
rs747864256 | in-del | -/TGA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069142 | GAAATGGAATCAGTC[-/TGA]GAGAGTTGGGCCTTC | 114088 |
rs747864289 | snp | C/G | 1.66638e-05 | 0.00288645 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094291 | TCAGCCTCCGGCTCA[C/G]ACGACCCTGGGCCGG | 114088 |
rs747895552 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081710 | ATCATCCCCTTCTCA[A/C]GTTTGATAATTCACT | 114088 |
rs747906315 | snp | C/T | 1.65422e-05 | 0.0028759 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000667 | TTAACAAGTACGTAG[C/T]GGGCTGTCTACTGAC | 114088 |
rs747916355 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994739 | TCAACAGATACTCTT[G/T]TGCAGATGGTTTCAA | 114088 |
rs747944236 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033045 | ACACTACTGGTCCTA[A/G]TCATTCTGGATAAGA | 114088 |
rs748002747 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993723 | TGTTTTCAGTCACCT[G/T]GCAGACAGACTTTGG | 114088 |
rs748009209 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001230 | AGCTGTGCTAATAAT[-/TT]TTTTTTTTTTTTTTT | 114088 |
rs748027418 | snp | C/T | 1.6476e-05 | 0.00287014 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000775 | TCCAGGACAACGTAG[C/T]GCTGTTGTTGTGGGT | 114088 |
rs748037455 | snp | C/G | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983000 | AAGGCATGGGGGAGA[C/G]AGATAGGAAGCAAAA | 114088 |
rs748112898 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050096 | TTACTAGTTACATAC[A/G]AAGAGTATTAAATCA | 114088 |
rs748152044 | snp | C/T | 1.64741e-05 | 0.00286998 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979394 | GTGCTTACCTGCACG[C/T]TCCTGTTCAGGCTGA | 114088 |
rs748179344 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987259 | AGCAATTCTTTGCTG[C/G]ACATACACTTCTATC | 114088 |
rs748214212 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081017 | AGGCCAGTCTTGATA[A/T]GATTTCCTCCCACGC | 114088 |
rs748217062 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066690 | ATTCAAAGCACTCCA[C/G]TCTGCTGCGTGGTCA | 114088 |
rs748232488 | in-del | -/GT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030587 | ATGAGTGTGCATATG[-/GT]GTGTGTGTGTATGAG | 114088 |
rs748252613 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017189 | TTTTAAATTTCTCAC[A/G]TGCCACCACTCTCCC | 114088 |
rs748264109 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999574 | ACTTAAACCTAGTGG[C/G]GGATCAAAAACACAT | 114088 |
rs748273669 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085519 | TTTTATATGGTGAAA[A/G]GTGGATCAGCTTTCT | 114088 |
rs748279153 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014732 | CATTTTGTGATCATT[C/T]ATTTCTACATTGAGT | 114088 |
rs748332881 | snp | A/G | 3.30207e-05 | 0.00406316 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981791 | CTTGGTTTGGGGGCT[A/G]CAGGGTACCTGTTGG | 114088 |
rs748356027 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072600 | ACTTTCTAAAATTCA[-/T]GTTTAATATGAAATC | 114088 |
rs748356748 | snp | A/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097389 | TGTAATTACAAGAAG[A/T]GGTAGGCACAATTAT | 114088 |
rs748363507 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072214 | TTTTTTTTCATAGGG[A/C]AACTTAACTCTCTCT | 114088 |
rs748425562 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016305 | GCAGGAGGTGAGCGG[C/T]GGCCACCTCCTTTCA | 114088 |
rs748451398 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083692 | GAATTCAGATCTGGG[A/C]ATCCTGAATGTGAGG | 114088 |
rs748491324 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009761 | TCTTATATTCAATCG[C/T]TTTCTGTCACTCTTA | 114088 |
rs748523545 | snp | A/G | 0.000124494 | 0.0078887 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986067 | GATTAAGGGTGGAGG[A/G]GAAAGGACTCATTCT | 114088 |
rs748549467 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088108 | TTTAACTTTTAACAT[G/T]TGCTTTAAGAATTAA | 114088 |
rs748562442 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980768 | GTAGGATTTGCTTTC[A/T]TGGTGAAATGGTGTG | 114088 |
rs748579470 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020434 | TGCTATGGGGGACAG[A/C]CAGCCACCTGTCTCT | 114088 |
rs748625849 | snp | G/T | 1.70956e-05 | 0.00292361 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094471 | TGCTCTGCTGGTAGC[G/T]GTCAATTACCCCTTC | 114088 |
rs748653764 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038047 | TGGTCCTCTAAAATG[C/T]CCATGCCCGAATCCC | 114088 |
rs748658484 | snp | A/G | 1.81322e-05 | 0.00301094 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977245 | CTTGCTGTGGCTCTC[A/G]CAGGCGGAGGTAAGA | 114088 |
rs748663834 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077575 | ATTTTTGTATATTTA[C/G]TAGAGATGGGGTTTC | 114088 |
rs748664405 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078740 | AAATAGTGGTTACCA[C/T]GGTGGGGAGAAAATG | 114088 |
rs748665406 | snp | A/C | 1.88781e-05 | 0.00307224 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094625 | GGCCGGTGGCGGCAT[A/C]GCCGGGGGAAACACG | 114088 |
rs748672092 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037119 | GTAACTGTGATTCCC[C/T]ATCACCTCACTACAT | 114088 |
rs748711776 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979999 | AAATGGTGTGAATTA[A/G]ATATCATTAAATACA | 114088 |
rs748714884 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039420 | CATGCATAAATAAAC[C/T]GTGTGTATTCACGCG | 114088 |
rs748718448 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055500 | ATGTAATCACAAGTC[C/T]CTTAAAAGTGGTAGA | 114088 |
rs748786568 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003809 | TCTATTCCTCCATGT[C/G]CTGAGAATTAGTTTT | 114088 |
rs748800546 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041929 | TAAACTGAATTCCAT[C/G]TAACCTTGTATCGCC | 114088 |
rs748816174 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081782 | TACTGGTTTATTATG[G/T]AGGATACAACTCAGG | 114088 |
rs748839501 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025342 | CTGACAGTCCGTTCA[A/G]CGCCTGGGAGAGCTG | 114088 |
rs748847182 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990348 | TTGTTCATTAGCCAA[C/T]GCTATTGAACACCTG | 114088 |
rs748855582 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980241 | AGTGAAATAATTATA[C/T]TCTGAGATGTAGTGA | 114088 |
rs748874519 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002920 | GTTTTAAGCTTCAAC[A/G]GCACAGGGTTTGGAT | 114088 |
rs748881861 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019608 | TATGGTATCATAGAA[A/G]ACAAGCCCCTGGAAA | 114088 |
rs748884852 | in-del | -/AT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993994 | CCCCAGAACCTGTGA[-/AT]ATGTTATTATCCATG | 114088 |
rs748897269 | snp | A/C | 0.00019982 | 0.00999351 | intron-variant, stop-gained, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986133 | GGAGGGTCTGTTCTT[A/C]TGAATCTGTGTCTAA | 114088 |
rs748897524 | snp | C/T | 2.11997e-05 | 0.00325567 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50998010 | CCACTTTAGATGCCA[C/T]GCAGTTCTCGCTCTG | 114088 |
rs748920175 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041508 | GTAGGGAATAGGTTT[G/T]AAAGCATCTCATAGC | 114088 |
rs748927449 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030036 | ACAGCATGACTAGTT[A/C]ACCTATGAAACATTC | 114088 |
rs748949824 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058521 | CCATTGAGATGTGGA[A/G]TGGGGAGTGGGACAT | 114088 |
rs748950338 | snp | C/T | 1.88799e-05 | 0.00307239 | intron-variant, synonymous-codon | TRIM9 | GRCh38.p7 | 14:50998021 | GCCACGCAGTTCTCG[C/T]TCTGAGGGATACTGC | 114088 |
rs749043748 | snp | C/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996137 | GTAACAGAGAATACT[C/G]ATATCTATATGATGA | 114088 |
rs749066810 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049586 | TAATCCCAGCACTTT[A/G]GGAGGCCGAGAGGGG | 114088 |
rs749069827 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983693 | CTTCCAAGTTCAATC[C/T]TTTCCTCTAAAGTTT | 114088 |
rs749078124 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023108 | AATAACTGGATAAAC[C/T]TTATTCTACAGTGGT | 114088 |
rs749124243 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035672 | GGCAGCCAGAGAGAT[A/G]TGTAGAGAAAACAGC | 114088 |
rs749136649 | snp | A/G | 0.000362665 | 0.0134611 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979504 | TTTTCTATTTAAGTC[A/G]AGGAGGACCCCAATT | 114088 |
rs749154523 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081485 | TGTGACTCAACAATT[C/T]CACTCCTAGGTATGT | 114088 |
rs749205309 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012631 | TTTTTTGAGGGATCA[C/T]CATACTGTTTTCCAT | 114088 |
rs749230270 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017292 | CACTGGCAAACTAAT[A/C]ACTTCAAAGGCAAGT | 114088 |
rs749245632 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040836 | GACCCTTAACTCTTC[C/T]GCTTACTACCACTGC | 114088 |
rs749247092 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063733 | AGAATTTTACATCCA[A/G]AGAAAATATCCTTCA | 114088 |
rs749249167 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050823 | GGATGCTCCCCATTG[A/G]ATCTCAGCCAGCACC | 114088 |
rs749292549 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984956 | CATTTTAAAGACAGC[C/T]TGAAGTCCCTGCATC | 114088 |
rs749337751 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057111 | TATCTGCATGGCCAC[A/C]GATGCTGTGCTCTCA | 114088 |
rs749341664 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977624 | GGAGATTGTGTTCCT[C/T]ATAACTGAAGACACA | 114088 |
rs749365103 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005905 | TGGGTCAGTTAAATC[C/T]GTAGCTAATAAGAGA | 114088 |
rs749379040 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097583 | CAAGCTCTGAATGTG[A/G]TAAGTACCCAAAATG | 114088 |
rs749384160 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072390 | AGTAGCCTACTTTCT[G/T]GCATAGAATCAGTTA | 114088 |
rs749444068 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017326 | AGGCTTTGCGGTTTT[A/G]ATCGAGAAAAGGATC | 114088 |
rs749449870 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016356 | TCTCACAGGAGCAGG[-/A]ACCCTACTGTGAACT | 114088 |
rs749449954 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068446 | GGAAGATAAAATAAG[-/AA]TAAATATCACATGAC | 114088 |
rs749477358 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002288 | CACCACGGCTGGCTG[-/A]TTTTTTTTTTTTCTT | 114088 |
rs749483873 | snp | A/G | 1.64863e-05 | 0.00287104 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982045 | GGTCACTGTCAGGTT[A/G]TCATTGGAGAGGATG | 114088 |
rs749501524 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034477 | ATTTAGAGTGACATA[C/T]AGGAAAGAAGTACAT | 114088 |
rs749519955 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045691 | AGGGCAGATCTAGTA[A/G]TCTGGATGTTTGTCA | 114088 |
rs749529920 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062823 | AACAGTAAAATAAAT[-/A]AGCAGAGATATCTGC | 114088 |
rs749588004 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073827 | TTGTTTTTTGCAGCT[G/T]CAGGCTTACATCATT | 114088 |
rs749632471 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999712 | AGACAGGGGTCTCCT[C/G]TTCATCAGTGCAGGA | 114088 |
rs749681471 | snp | A/T | 1.94195e-05 | 0.00311599 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094651 | ACACGCGGACGCCGT[A/T]GGGGGACTTCTGGCA | 114088 |
rs749688320 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077696 | ACCACTCCCGGCTGT[C/G]CTAAACCAATTCTAA | 114088 |
rs749690255 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090586 | TTGTTACAAATATGT[A/T]ACTGATTCAGTGACT | 114088 |
rs749706159 | in-del | -/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996707 | TGAGAAAAGAGGCAA[-/C]TGCTCTCAAACTGAT | 114088 |
rs749713945 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038174 | GTCCTTAAAAGCAGA[A/G]GAACTTTCCTGACTG | 114088 |
rs749725207 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055418 | ATAAATAGGTCACAT[A/G]GCAAAAGAGAATTAA | 114088 |
rs749732800 | snp | A/G | 1.97058e-05 | 0.00313887 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094818 | GATTCAGACTCTGGG[A/G]TCTGCACCAGGATGT | 114088 |
rs749744176 | snp | A/G | 3.31033e-05 | 0.00406823 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009245 | AAATCTAATCAGATA[A/G]AGAGGACCACAGCCT | 114088 |
rs749758761 | in-del | -/TTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077398 | CTGTTTTTTTTTTTT[-/TTT]TTTTTTTTTTTTGAG | 114088 |
rs749759112 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988253 | AGTGCATTGAATTCC[C/T]AAGCAGTTATCTGAA | 114088 |
rs749768159 | in-del | -/CT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047328 | GACAGTCAGTCATCA[-/CT]CTGACAGCATCTGGG | 114088 |
rs749873556 | snp | A/G | 1.66963e-05 | 0.00288927 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094121 | CTTAGGACTCACCTT[A/G]TGTAGTTTCCACATG | 114088 |
rs749878545 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977931 | GTCTTCTCCAGCCCA[A/G]GAGTCTTTATCAATA | 114088 |
rs749879753 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089067 | AATTCACTGAGATTC[A/G]AAGATTTGTTACTGG | 114088 |
rs749998289 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006182 | AAAATATTTTAACTT[C/T]CTCCTGTAATCAACT | 114088 |
rs750032734 | snp | C/T | 1.64933e-05 | 0.00287165 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094233 | CAGTACATGCTGTGG[C/T]TCTCCAGCTCGTGGT | 114088 |
rs750041212 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074147 | CTAATAGCTGGGTGC[A/G]GTGGCTCACGTCTGT | 114088 |
rs750048475 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994219 | GAGACAAACCTGGGC[A/G]ACACAGCAAGACCAC | 114088 |
rs750095606 | snp | G/T | 0.000183604 | 0.00957958 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000752 | CACCGTGGACAGAGG[G/T]GGCTGTTTCCAGGAC | 114088 |
rs750105730 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073634 | CTTGCCAAGAGTGTG[A/G]TGTGGGCGCTCTGGA | 114088 |
rs750123707 | in-del | -/CAAAAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068333 | GGTGTGCACCAAAAA[-/CAAAAA]CAAAAACAAAAACAA | 114088 |
rs750213825 | snp | C/T | 6.03045e-05 | 0.00549078 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094922 | GGGGCATTTCAACTC[C/T]TCTTCCATCTCCTCC | 114088 |
rs750221599 | snp | A/G | 1.65908e-05 | 0.00288012 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010359 | GGACATTTAGAATCT[A/G]ACGCAGAAACTAGTT | 114088 |
rs750260229 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010651 | AGTGTCTGCTGGGGA[A/T]AAGGGCTCTGGAAGA | 114088 |
rs750280155 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980795 | TGTGTGTGTTCACTT[C/T]AAGTGACAGCGAATA | 114088 |
rs750281071 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031555 | TAACTCTGAGCCCCT[A/G]CTCAACCCCTTTCCT | 114088 |
rs750316740 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054945 | AGTGATTCTCCTGCC[C/T]CAGCCTCCTGAGTAG | 114088 |
rs750319005 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015919 | TTTCAAAAAGTTCTT[C/T]CTTAAATATAAGCTA | 114088 |
rs750319131 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027315 | CACCGAGTGAACTTT[C/T]GTATTTTTAGTAGAG | 114088 |
rs750335318 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066347 | TCCATCTTTGCAAAC[A/C]CAAAGGTCAGTACTT | 114088 |
rs750346549 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981901 | CACATCCTTCATCAC[A/G]TCCATGCGAGCCACA | 114088 |
rs750348279 | snp | A/G | 1.68136e-05 | 0.0028994 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010520 | AAAAAAAACAACAGA[A/G]CAGTCCAAGATGGCA | 114088 |
rs750372995 | snp | C/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096852 | GCAGGATACACTTAA[C/T]TTATAGGTCCCAAGA | 114088 |
rs750399710 | snp | A/G | 3.29495e-05 | 0.00405877 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981991 | GCCCTTGGAGAAGCC[A/G]GTCTTCCCTAGCACC | 114088 |
rs750426234 | snp | A/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095425 | CGACCTCCGGTGCAG[A/T]CTCCCAGGAGCTGGG | 114088 |
rs750449668 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020199 | GGCAAGTGATGTCTA[C/T]AAAAGGCCAGTCTTT | 114088 |
rs750583380 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058834 | GATTTGTTATAAGCT[G/T]TTGGAAGAATAAGAA | 114088 |
rs750601547 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048470 | TTTGTCTGCCTGTCC[A/T]TCCATCAAATCCTGA | 114088 |
rs750607025 | snp | A/G | 0.000755287 | 0.0194184 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985969 | ACCCGGTGCATTGAG[A/G]GACTGTAAAGAGGAA | 114088 |
rs750613310 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090239 | TATGCTGCCTGTTAC[A/G]TTTACCACAGGAATA | 114088 |
rs750614877 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076893 | GCAGTAGACCCTGGA[A/C]CAGATTCTAGTTTTC | 114088 |
rs750618870 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075746 | CTCCACCTCTCAAAA[-/C]TTCCCAAGGCGGGGA | 114088 |
rs750630960 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053382 | AGTGCACACTCATGA[-/T]AGGAGATGCTTCAAC | 114088 |
rs750644328 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047681 | AGTACAGGAAAGAAA[C/T]GCATATAACAATCTG | 114088 |
rs750690692 | in-del | -/AC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999367 | TTACACACACACAAC[-/AC]ACACACACACACACT | 114088 |
rs750692294 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981424 | TTTATTGTACTAATT[G/T]GATGGATTTGGAAAC | 114088 |
rs750706083 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059982 | ATGATACAAATTGTT[G/T]CTTAAAAAAGTGTTT | 114088 |
rs750713755 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081644 | TTCCAGTTGCCAAGT[A/C]CTGGGTCCCCAGGCT | 114088 |
rs750739777 | snp | C/T | 1.64904e-05 | 0.00287139 | intron-variant, synonymous-codon | TRIM9 | GRCh38.p7 | 14:50979369 | ACAGCTGTTTAACCT[C/T]AGGGGCAGGGTGCTT | 114088 |
rs750740333 | snp | A/T | 1.6483e-05 | 0.00287076 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000833 | GGTTGCTGGGACTGG[A/T]GAGGAAGCTAAACAG | 114088 |
rs750789631 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014635 | TTAAATCAGATCTTT[C/T]AAGAGTATAAATACT | 114088 |
rs750795249 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979440 | GGCCCTCCACGTTAT[C/T]AAATGCTATGGGACC | 114088 |
rs750872165 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042603 | TGACATTAATTTTAC[A/C]CTGATGTTACAAAGG | 114088 |
rs750874649 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029556 | AAATATTGATCTCTG[G/T]GTCACATTGCTCAGC | 114088 |
rs750879814 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024839 | AAGAAAAAAAGGAAG[A/G]CAGGAAGGAAATGAA | 114088 |
rs750950025 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041476 | TTAGGAATGTCAATG[A/T]TGTTTCAATCTCAGG | 114088 |
rs750961230 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070784 | AAATGGCACAGTGTA[C/T]TTGTTTCTGAAGGTA | 114088 |
rs750998417 | snp | A/G | 1.64732e-05 | 0.0028699 | stop-gained, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022879 | CGCGGGCCAGCAGCT[A/G]GGCTTTTCTTCTGTT | 114088 |
rs751036446 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074216 | TTGAGCCCAGGAGTT[C/G]AAGACCAGCCTGGGC | 114088 |
rs751044377 | snp | A/G | 1.68204e-05 | 0.00289999 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094394 | GACATCGCACTGTTC[A/G]CACATGACGGTGGCT | 114088 |
rs751048253 | snp | C/G | 1.64779e-05 | 0.00287031 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000765 | GGTGGCTGTTTCCAG[C/G]ACAACGTAGCGCTGT | 114088 |
rs751050160 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996630 | GGCCATCACCAGCAA[A/G]GGCCTTCTGCGTTGC | 114088 |
rs751054634 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995572 | TCACAGAGTACAAAA[C/G]ATGAGCAATTTAAAC | 114088 |
rs751110000 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049323 | GATTATACCAGGTCT[C/T]ACTGTGACTTGCAGT | 114088 |
rs751149890 | snp | C/T | 4.94181e-05 | 0.00497057 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979467 | GACCTTGTTGTTCAT[C/T]GTTGATAAAAAATGT | 114088 |
rs751159840 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063546 | TACACATACATATGA[C/T]AGTCAAAGTCCTAAA | 114088 |
rs751171171 | snp | C/G | 9.9108e-05 | 0.00703876 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000863 | GAAATTAGTGTAACT[C/G]TGGCTTCTGTTAAGC | 114088 |
rs751174374 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982182 | ACTCCTGGGCGGGTG[A/G]GGAGCGTTGTGTAGC | 114088 |
rs751178361 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075027 | TCCAAAGAGACTCTT[A/G]TCAGGAACTGAGTCA | 114088 |
rs751194150 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976805 | TAAGAGGGTAAGAAC[A/G]TTCTAGCAGGTAAGC | 114088 |
rs751201587 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050525 | TCTTGTGTATGTCTT[C/T]ATCAGCAGCATGGGA | 114088 |
rs751226245 | snp | C/T | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009130 | TGCAGCAGAGGGCTG[C/T]TGTCCAGACTCAAGT | 114088 |
rs751252827 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996780 | GAAGCTGTAGCTACC[A/G]CATCACTGTACTCCA | 114088 |
rs751255777 | snp | C/G | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983369 | AAGATAATTACAATA[C/G]GTATACTTGCCTAAT | 114088 |
rs751265486 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983452 | ACACATCAACGCTAT[A/G]AAACAACAACCAGGT | 114088 |
rs751323994 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080614 | TTCTAACTTTGCAGA[G/T]GGTTGAGCAAATGAT | 114088 |
rs751351377 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017003 | TGTCCTAAAGCATGA[C/T]GACCAACTGATGCTT | 114088 |
rs751394921 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045397 | TAACGTAAGATAGAA[C/T]TTTCACCTTTTAGAG | 114088 |
rs751412691 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037234 | TTAAATGTATAAATT[A/G]TCTAGATATTAATAC | 114088 |
rs751413250 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018365 | CCTTCCTCCCTCCCC[C/T]CTTTCTTTCTTTCTT | 114088 |
rs751413619 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987935 | CCTCCAGAGTAGCAG[A/G]GACTACAGGCGTGAG | 114088 |
rs751438328 | snp | A/G | 3.43354e-05 | 0.00414325 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982115 | GCCACTGGGAACAAC[A/G]GAAGGGAATCAGGTT | 114088 |
rs751461383 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005568 | AACCAAACAGTAAAG[A/C]CCTTGGCTGACTAGG | 114088 |
rs751484454 | in-del | -/AGTGT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990066 | GGTCATCCAGGCTAG[-/AGTGT]AGTGTAGTGGTGTTG | 114088 |
rs751527866 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982513 | TCCTAGATGGAGGAG[C/G]GATAAAACACATGGA | 114088 |
rs751564469 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010956 | CATCACCATCTGAAC[A/C]CAGTTCCTTTCCCTT | 114088 |
rs751594112 | snp | A/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978213 | GAAACACAACAATGA[A/T]TTTTGATAAATAGTT | 114088 |
rs751638868 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060579 | TCACACCATTCTCCT[A/G]CCTCAGCCTCCCAAG | 114088 |
rs751670116 | snp | A/T | 1.7616e-05 | 0.00296778 | missense, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977302 | ATCCTTAGGCTATTG[A/T]TGCTCTGCTGGAGTA | 114088 |
rs751686236 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024670 | CTAGATAAAGCAATC[C/T]GAAATTATAGTTGCC | 114088 |
rs751696965 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021256 | AACAAGACCACAGTG[C/T]ACATGTGCTAATCAC | 114088 |
rs751721957 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009437 | GAACACTTTTGTGAG[G/T]TGGGGGGCACTATAA | 114088 |
rs751723003 | in-del | -/GGTA | 3.2993e-05 | 0.00406145 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981794 | GTTTGGGGGCTGCAG[-/GGTA]GGTACCTGTTGGTGT | 114088 |
rs751731631 | in-del | -/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096910 | AGTATTAATTGAATT[-/G]TAATGAAAGTTAATT | 114088 |
rs751800047 | snp | A/C/T | 3.89433e-05 | 0.00441253 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094791 | GAGCCCGCGGCCCGA[A/C/T]GGCTCTGGGGGGATT | 114088 |
rs751805595 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079801 | CCTAGAGCTAGATGA[A/G]AAGACTGTACACAGG | 114088 |
rs751824591 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070886 | TTGACTCACATTCCT[A/C]GACGTTTTCTTTCTT | 114088 |
rs751863297 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037841 | CTTAGCCTGCAGGAC[A/G]CCTTGGGAGGGTAAA | 114088 |
rs751864139 | snp | A/G | 3.3404e-05 | 0.00408667 | intron-variant | TRIM9 | GRCh38.p7 | 14:50979561 | AGTTCTGTAGGAAAA[A/G]AGAAAAATTGGGGTT | 114088 |
rs751878566 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083325 | GGTGTAATCATGGCT[C/T]ACTGTAATCTCGAAC | 114088 |
rs751963919 | snp | A/G | 0.000115589 | 0.00760138 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025216 | CTCTCCCGCCACACA[A/G]TTACGTATTAACCGG | 114088 |
rs752001286 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020387 | ACAGCAGAAAAACAA[A/G]TCATTCGAGATAGAA | 114088 |
rs752083801 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031020 | AGGCATGGTGGCGGG[C/T]GCCTGTAACTCCAGC | 114088 |
rs752113735 | snp | C/T | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025287 | TGCTGGACCATGTTG[C/T]GCAGCTGTACCAGAA | 114088 |
rs752131682 | snp | A/G | 4.94393e-05 | 0.00497164 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009154 | CTCAAGTCAAAGTCC[A/G]TGGTCATCCTTGGAG | 114088 |
rs752132223 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043691 | TTAACAGAACTGTGC[A/T]GCTCACTAATTATAT | 114088 |
rs752136261 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051969 | CCCTGTCTTGAAAAG[-/A]AAAGAAGGAAAAGAG | 114088 |
rs752200245 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984695 | TGAAATCTTTTTACA[C/G]TACTTTAAATACATT | 114088 |
rs752200914 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076592 | ATCCAGTCCTCATCA[C/T]CACCCTGGATCTAGT | 114088 |
rs752202038 | snp | C/G | | | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998079 | AGGACCAGGGTCTTG[C/G]TGTACGGGCTGACTC | 114088 |
rs752215708 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023814 | AAATACTCACATATA[C/T]GTTAGTAATACTTAA | 114088 |
rs752216737 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997094 | AGTTATGGAGAATCC[C/T]GGTGAGGTGGGGGGG | 114088 |
rs752230466 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024900 | TACCATTAAATGATA[C/T]AATTATTACAAGGTG | 114088 |
rs752322546 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036446 | AGTTTCTGTCTCTAG[C/T]GATAAGTGGAAAAGG | 114088 |
rs752380099 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060128 | TCTAGCTTTCTGTTG[-/T]TTCTTTCCACAGACT | 114088 |
rs752383686 | in-del | -/CAGCTGC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058647 | ATGGCCCCAAGACCA[-/CAGCTGC]CAGCTGCCTAGACCT | 114088 |
rs752392491 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093696 | GCGACCCCACCGCCC[C/G]CATCCCAGTCCCTCC | 114088 |
rs752401185 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064416 | AGTGTAACTACTCCA[A/G]TTAAAAGGTAAAGAC | 114088 |
rs752401694 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019059 | TTTCTGAAGAAAGCA[C/T]AGATTTCATTAATGG | 114088 |
rs752434334 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018565 | TGGTAAATAATAACA[A/G]AGATAATGGTGAAAA | 114088 |
rs752484668 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984656 | AATCATGCCTTGTGC[-/A]ACTCTTTTTCAAAAC | 114088 |
rs752505360 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091434 | TTGATAACTAACTGC[C/T]CAATTTTGGAAACCT | 114088 |
rs752506338 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006439 | ATATTACAGAGGCCA[A/G]TAGAAGTCTGAACTC | 114088 |
rs752535194 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057932 | AATTTATTGAAAGGA[C/T]AGACTTTTGGGCTCT | 114088 |
rs752570101 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047365 | GCATTCATTTCATCA[C/T]GGCTGTTTCCCACTG | 114088 |
rs752581237 | snp | G/T | 3.59764e-05 | 0.0042411 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094553 | GCTGCGGTGACACTG[G/T]GGGCAGGTGATACAG | 114088 |
rs752590563 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995752 | AGAACGCACCACCCC[A/G]CCACCCCCAATACCA | 114088 |
rs752607885 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043975 | AAGTTAAATGACATA[-/T]TTAGGATCCAAAGAG | 114088 |
rs752648346 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075339 | TTATTTCATGTAATT[A/C]TTTTTCTTGTTTATT | 114088 |
rs752649878 | in-del | -/TTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027134 | TGCTGGCTGTTAACT[-/TTTTTTTTT]TTTTTTTTTTTTTTT | 114088 |
rs752655020 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981469 | CGAAGTAACTTGCCC[A/C]AAAGTGCTTTTCTGT | 114088 |
rs752664434 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046471 | ACTGGGAAAAGTGTC[A/G]AAGGGATTTCTGTAC | 114088 |
rs752685348 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072834 | AATATCTGACAATGA[C/T]TTGATAGAGAGCAAT | 114088 |
rs752745124 | snp | C/T | 1.67365e-05 | 0.00289275 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979341 | TGGGCAGCCTTTGAA[C/T]CGGTAGCCAGCAACA | 114088 |
rs752754816 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006048 | CGGCAACAACAATGG[C/T]GTCTATGATGAGCTT | 114088 |
rs752755417 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050400 | CTCATTGCCTCTTTG[C/T]CTGCCACCATGTAAG | 114088 |
rs752794266 | snp | A/C | 1.96046e-05 | 0.0031308 | stop-gained, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094807 | GGCTCTGGGGGGATT[A/C]AGACTCTGGGGTCTG | 114088 |
rs752810322 | snp | C/G | 5.61057e-05 | 0.0052962 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094956 | GGGACCGGTCTGGGA[C/G]GAGACAGCGACGGCT | 114088 |
rs752828952 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987342 | GAATATCATCCTATG[C/T]GAAGAGCTCTGAACA | 114088 |
rs752866980 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038881 | TCAGTTCAGAAGCCT[A/T]AAGTGATGTATGTTT | 114088 |
rs752878300 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984375 | AAAAAAGGACTAATG[A/G]CTGAGTTAAAAACAA | 114088 |
rs752909644 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057070 | AAGCATTCATTTGGG[C/T]AGCCAGCATAGGCTC | 114088 |
rs752974248 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081341 | ATAAAAAGGACAGAC[A/G]ATTACAAGTGTTAGT | 114088 |
rs752993860 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027756 | GAGGGAAAAACGGTC[C/T]CATTTGGAAGAGCAG | 114088 |
rs753000319 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981689 | CTACTTAATGTAGAC[A/C]ACCTGTTTGATTTCC | 114088 |
rs753011446 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073448 | AAACATTCATAAAAA[C/T]GGAATACCATACAAC | 114088 |
rs753087989 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025331 | TTTGGCCCTGTCTGA[C/T]AGTCCGTTCAGCGCC | 114088 |
rs753102695 | snp | C/T | 3.86653e-05 | 0.00439672 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50998019 | ATGCCACGCAGTTCT[C/T]GCTCTGAGGGATACT | 114088 |
rs753161081 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011008 | ACGGTCAATTGTTCT[C/G]CATCTTTTTCCTTGC | 114088 |
rs753170029 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002288 | ACCACGGCTGGCTGA[-/TT]TTTTTTTTTTTTCTT | 114088 |
rs753204730 | snp | A/G | 1.74909e-05 | 0.00295722 | missense, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977332 | AGAAGTCGGGGACTG[A/G]GAGCCCGGTGTGCAG | 114088 |
rs753210649 | snp | A/G | 1.75084e-05 | 0.0029587 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094069 | GTCTGCTGCAAAACC[A/G]GATGATCGGAGACGC | 114088 |
rs753230794 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091559 | TAAACTATATGAGAA[A/T]ACTGGCTGCTAACAC | 114088 |
rs753231788 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049889 | AATAATCTGGGCAGA[C/G]GAAATGGCTCTGGTA | 114088 |
rs753278189 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981870 | TTGCCCAAGCTTTGT[C/T]GTCTTTTCCTAACAT | 114088 |
rs753278617 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031105 | GTGAGCTGTGATTGC[A/G]CCATTGCACTCCAGC | 114088 |
rs753279665 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976193 | CTGACATCATTTCTA[C/T]CAAGAAGGGCTCTGT | 114088 |
rs753313295 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986192 | GAAGTCTGCTATTAT[G/T]TCCCCGTGCACGGTT | 114088 |
rs753325895 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987712 | TACAACACCCAAGCA[C/T]CACAAACTGGCATGG | 114088 |
rs753346084 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014789 | CCAGGCCACCTCACT[C/G]TTGTCTTTGAATGAC | 114088 |
rs753356740 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015786 | ATTGGGATTACAGGC[A/G]TGAGCCACCACACCT | 114088 |
rs753378805 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063302 | ATTCAATCTGACAGA[C/G]AGAGGAAAAAAGTTT | 114088 |
rs753387142 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071152 | GAGGCCAGGGTGGGC[A/G]GATCACCTGAGGTCA | 114088 |
rs753400495 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026094 | GGGAGGCCGTGGTAC[A/G]CAATCCTGACGGACG | 114088 |
rs753443199 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052924 | CATTTTGGGAGGCTG[C/T]GGTGGGCAGATCACT | 114088 |
rs753547974 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977166 | AGACTGCAGAGGACC[A/G]GCTTTTCTCTCCTCC | 114088 |
rs753560659 | snp | C/T | 5.32874e-05 | 0.00516148 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977290 | CCTCCACGGCACATC[C/T]TTAGGCTATTGATGC | 114088 |
rs753571973 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054800 | TGCCTCGGCCTCCCA[A/C]AGTGCTGCGATTACA | 114088 |
rs753626960 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034926 | CTTGCTGGGTTGTAT[-/A]AAAGCCTGGGCAGGC | 114088 |
rs753656694 | snp | C/G | 1.84995e-05 | 0.00304128 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094591 | GGGGCACCGGGGCCA[C/G]GGCCGGTGACAAGTG | 114088 |
rs753687782 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980394 | TCTAGCAATATTGAA[C/G]TTCGTCCTCATCTCA | 114088 |
rs753695549 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020009 | CATTCCTAGTTTTTT[G/T]GATTGCTCAAGGAGA | 114088 |
rs753706514 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037604 | CAATAATTTCAGGGT[A/G]TCTTTATTCCAGTAT | 114088 |
rs753710456 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047453 | ACACAGAGCTTAGAA[A/T]ACCATTCGGTGCAAT | 114088 |
rs753725749 | snp | C/T | 4.99471e-05 | 0.00499711 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010342 | CTAGACTATGTCCTA[C/T]GGGACATTTAGAATC | 114088 |
rs753752971 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047961 | TGAGACCCTGTCTCA[-/A]AAAAAAAAAAAAATC | 114088 |
rs753762298 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998251 | AGGGGCGAGGGAGGC[A/G]GTGTCGCTCAGTGGT | 114088 |
rs753781272 | snp | C/T | 5.80074e-05 | 0.0053852 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094758 | TCCAGGTCCAGATAG[C/T]CATAGTCGGAGACCC | 114088 |
rs753836329 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029476 | AACACTCAGGAAAAA[A/G]GTGATCATTGATGCA | 114088 |
rs753843262 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053534 | TTTTTTTTTTTATGC[A/G]TTAACATTACATTTA | 114088 |
rs753863577 | in-del | -/A | 0.0132536 | 0.080319 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010503 | GAACCACCTAGGATT[-/A]AAAAAAAAACAACAG | 114088 |
rs753913200 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990580 | AAAAGGTAGCCTTTG[A/G]GGTGTTATTTTTGGA | 114088 |
rs753930255 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041262 | GAATTAGTTGATTTT[G/T]TAAATGACAAAATAA | 114088 |
rs753931553 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002444 | CGGCTGGGAACCATG[C/T]TTTTGCCAGCTGCTT | 114088 |
rs754007183 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058063 | AGATTATAGTAATCT[A/G]ACAGCCTATCAGTAA | 114088 |
rs754016402 | snp | G/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022869 | TCCTTGTTGACGCGG[G/T]CCAGCAGCTGGGCTT | 114088 |
rs754096173 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991761 | ATTGTAAAGACTCAG[A/G]GGTCCTCAGCTGTAA | 114088 |
rs754119300 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011729 | CAAAACAATCAGGAA[A/G]TAGATGAGAAAAAGC | 114088 |
rs754133642 | snp | C/T | 8.2411e-05 | 0.00641862 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094211 | CACGGGCATCTTGCA[C/T]TGCACGCAGTACATG | 114088 |
rs754162638 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995443 | GCACTGCCCAATAAA[C/T]AGACAGATAAATTTG | 114088 |
rs754203210 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027766 | CGGTCTCATTTGGAA[C/G]AGCAGGCAATAATAT | 114088 |
rs754238469 | snp | C/G | 1.65542e-05 | 0.00287695 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998210 | GTCAGCAAAGAACAG[C/G]ACAGCACTTAGCCTG | 114088 |
rs754265334 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982689 | CAGGTTGCTGTCTGC[A/G]TAACTTAAAAAACAC | 114088 |
rs754288157 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051468 | GAATTTGGGACAGGT[C/T]GGGTGAGGGCAGGCA | 114088 |
rs754295721 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983063 | TAGACTAGTACCCCA[A/G]AAGGACTCAATTTAA | 114088 |
rs754306593 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000410 | TAGGCATTGTCCACA[C/T]AGCTAGGGTGGAGGA | 114088 |
rs754363497 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081415 | ATGTAAGATGGTATA[A/G]CTTCTTTGGAAAACA | 114088 |
rs754378048 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050427 | TAAGACATGCCTTTC[A/G]CCTTCCACCATGATT | 114088 |
rs754408931 | snp | G/T | 8.5767e-05 | 0.00654799 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094969 | GAGGAGACAGCGACG[G/T]CTGCAGCGGGTGCCT | 114088 |
rs754417690 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092164 | AAAAAACTAGCTGTG[A/G]ACTCAAGTTTTGAAA | 114088 |
rs754451004 | snp | A/C/G | 3.30979e-05 | 0.00406793 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979352 | TGAACCGGTAGCCAG[A/C/G]AACAGCTGTTTAACC | 114088 |
rs754504649 | snp | C/T | 4.97772e-05 | 0.0049886 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000889 | TAAGCTGCAGATATT[C/T]CAGTATCTTAGAATG | 114088 |
rs754529916 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995691 | TTTGAAAAGGGATTA[A/G]CTCTTGCTAAGAAGA | 114088 |
rs754566075 | snp | C/T | 4.94222e-05 | 0.00497078 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979392 | GGGTGCTTACCTGCA[C/T]GTTCCTGTTCAGGCT | 114088 |
rs754598949 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984604 | GCTTGGAAATAAGTT[C/T]GTAGAATCTGAATAG | 114088 |
rs754626881 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003705 | TGTCCCAGATTTAGA[-/C]CAAATTAGCAAATGG | 114088 |
rs754654949 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050566 | ACAATGTCTTTAACA[A/G]TGTGACCCTCCAACA | 114088 |
rs754676010 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013429 | ATTTTGATTATTGTC[A/G]CTTTATAATAAGGTT | 114088 |
rs754683784 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017094 | AAAGAATTCTCTTGT[G/T]TTTTCCAAGAGTAGA | 114088 |
rs754694542 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023720 | AGTTATTAAGGATAA[A/G]CTTTTCAATGAGTAA | 114088 |
rs754694629 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012097 | ATGACATTTTCCACT[G/T]TAACCATTTTCAAGT | 114088 |
rs754709707 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056736 | CCAGGATCATAATTG[C/T]AACTGGCCCAATATC | 114088 |
rs754729435 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063550 | CATACATATGACAGT[C/T]AAAGTCCTAAAAACC | 114088 |
rs754757428 | snp | G/T | 1.74108e-05 | 0.00295044 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982124 | AACAACAGAAGGGAA[G/T]CAGGTTATTAAGACA | 114088 |
rs754766929 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001231 | GCTGTGCTAATAATT[-/T]TTTTTTTTTTTTTTT | 114088 |
rs754791318 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055058 | CTTGATCTTGACCTC[A/G]TGATCCGTCCGCCTC | 114088 |
rs754817206 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084672 | GGGATAACATTATTC[C/T]AAGATAATGGGACAG | 114088 |
rs754855505 | snp | C/G/T | 8.32139e-05 | 0.00644987 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094287 | GGGCTCAGCCTCCGG[C/G/T]TCACACGACCCTGGG | 114088 |
rs754860017 | in-del | -/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978123 | GATTAGATTCCAGCC[-/T]TCTAGAAAACCCCAT | 114088 |
rs754869636 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068839 | GTCTCTTCTGATAAG[C/G]TCCTGAATAAACTGT | 114088 |
rs754876198 | snp | A/C/T | 3.53346e-05 | 0.00420313 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977348 | GAGCCCGGTGTGCAG[A/C/T]GTGACCTGGGGAATG | 114088 |
rs754880263 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988866 | TTAGATTTCAGGAGT[C/T]TTAGAGGGAAGAAAC | 114088 |
rs754909016 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995075 | CAGGCAGGATTCAAA[C/T]TCCTGGGCTCACAGG | 114088 |
rs754916397 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005626 | CCTGGAAAAGAGCTG[A/G]TCATACAACCTTAGA | 114088 |
rs754980095 | snp | A/C/T | 3.36345e-05 | 0.00410077 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094402 | ACTGTTCGCACATGA[A/C/T]GGTGGCTTCCTTGGG | 114088 |
rs755016544 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086047 | TAAATTTATTTTGTC[A/G]CAAGGAATCTTAGGA | 114088 |
rs755018508 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073672 | GGAGCATGCAGGGGG[C/T]TTCTGGAGGCTGATG | 114088 |
rs755021931 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077285 | ATAGGTGAGACAGTA[C/T]AGGTGACACAGTGGC | 114088 |
rs755021967 | snp | C/T | 1.87075e-05 | 0.00305833 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094613 | TGACAAGTGGGTGGC[C/T]GGTGGCGGCATAGCC | 114088 |
rs755039032 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049680 | AAACTACAAAAATTA[A/G]TTGGGTGTGGTGGTG | 114088 |
rs755042689 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037953 | AACACTGAGAGTCAG[G/T]TTCAGCCAATGGAAT | 114088 |
rs755052448 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998420 | GGATTACTTAATGTT[G/T]TATATGCAGATTAGC | 114088 |
rs755059583 | in-del | -/GGGAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069061 | GGTGAAAGGACATAG[-/GGGAC]GGGACTATGGTAAGG | 114088 |
rs755074297 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078652 | CTGTACAACATACAA[C/T]GATATTGTATGATAT | 114088 |
rs755090870 | snp | G/T | 1.74738e-05 | 0.00295577 | missense, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977321 | TCTGCTGGAGTAGAA[G/T]TCGGGGACTGGGAGC | 114088 |
rs755130920 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062288 | TACCAACATCTGGGC[C/T]ATCTTTGGGCATGCC | 114088 |
rs755135373 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010976 | TCCTTTCCCTTCCTG[A/C]CCCTCCCCACAGCCC | 114088 |
rs755234265 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066682 | CAGAGCACATTCAAA[A/G]CACTCCAGTCTGCTG | 114088 |
rs755238977 | snp | A/G | 1.64871e-05 | 0.00287111 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009206 | GATCCTCAGTCAGGT[A/G]CACTCTTCTTATGAG | 114088 |
rs755281627 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071592 | ATGATCGCTTGAGCT[C/T]AGGAGTTCAGGGCCA | 114088 |
rs755286698 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026649 | TTGGTGCTGTGAATG[C/T]TTTTCTCTTATATTT | 114088 |
rs755299436 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031039 | TGTAACTCCAGCTAT[G/T]CAGTAGGCTTAGGCA | 114088 |
rs755310756 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038775 | GTGAAGCTTCTCCGT[C/G]AGTCTGGAATCAACT | 114088 |
rs755383771 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981540 | TCTTATAATGGATAT[C/T]CATTGGGATTCTTAG | 114088 |
rs755384956 | snp | C/T | 1.65192e-05 | 0.00287391 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025220 | CCCGCCACACAGTTA[C/T]GTATTAACCGGCGGG | 114088 |
rs755393831 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089424 | AGGACAAATGTTCCC[C/T]GTACATTATTTTCAT | 114088 |
rs755436963 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009759 | TTTCTTATATTCAAT[C/T]GCTTTCTGTCACTCT | 114088 |
rs755465257 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074156 | GGGTGCGGTGGCTCA[C/T]GTCTGTAATCCCAGC | 114088 |
rs755473705 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021297 | CCTGACAGCTTTGCC[A/G]ATTCCTGCAGGTAGG | 114088 |
rs755489454 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020394 | AAAAACAAATCATTC[A/G]AGATAGAAGACAGAA | 114088 |
rs755500551 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096206 | TCCAACGAGGGGCAT[A/G]GTGAGGCGGTGATTC | 114088 |
rs755521605 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076174 | CCGAGGTACAGATGG[G/T]ATAAATAACTTACCA | 114088 |
rs755567594 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002049 | GAAATATTAGTTACT[A/G]AATAATCCCAGTTCT | 114088 |
rs755573457 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992883 | TTCAAGAATCCCAAC[A/C]TATTTGTCATTAGAT | 114088 |
rs755586885 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093927 | CTCTGTGGGGGCATT[C/G]AACTCCCCCGTGCGC | 114088 |
rs755640274 | snp | A/G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092760 | CATGAGGCTTATTTC[A/G/T]TTTATGTCTGTGTGT | 114088 |
rs755648561 | snp | A/C | 8.31968e-05 | 0.00644914 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981749 | ACTGGGGCTCTCACT[A/C]CTGATCAGAAGCCAA | 114088 |
rs755742260 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029899 | CACCCTCACAGGCCA[A/G]AACAATTGTTTAATT | 114088 |
rs755762091 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063078 | GCCTCAAAACAGCTA[C/T]GATAAAGATGTTCAA | 114088 |
rs755770847 | in-del | -/GCCCGCCTCG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040026 | CTGACCTCCTGATCC[-/GCCCGCCTCG]GTCTCCCAAAGTGCT | 114088 |
rs755771719 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042870 | CCTTCTCTGGGTAAA[A/C]ACAACCTCCCCTGCC | 114088 |
rs755792298 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041831 | ATAATGTTTAATAAA[C/T]ATGTTTTCCCAATAA | 114088 |
rs755813729 | snp | C/T | 1.65113e-05 | 0.00287322 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025228 | ACAGTTACGTATTAA[C/T]CGGCGGGTTTCCTTG | 114088 |
rs755833919 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014742 | TCATTTATTTCTACA[C/T]TGAGTTTTTCATAGA | 114088 |
rs755872017 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086082 | AATGACTCAATTTCT[C/T]AGTAATTTTCATATA | 114088 |
rs755907234 | snp | C/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996935 | AGGATTCAAAATTGT[C/G]CTTGTTTTTAACCAT | 114088 |
rs755911584 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006461 | TCTGAACTCCAGCCA[A/G]TCAAGTTCTATTGTG | 114088 |
rs755929695 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087122 | TCCACAGCTGTGGAG[G/T]CTGACTCATCTCAAC | 114088 |
rs755929985 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979609 | TCTAGAAGCTCCCCC[A/C]TTTTGTGTGGTGAAA | 114088 |
rs755930336 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091476 | TTCTTTGCTGTCCTA[A/T]TTTTGCAGGGCATAG | 114088 |
rs755930734 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069146 | TGGAATCAGTCTGAG[A/G]GAGTTGGGCCTTCTT | 114088 |
rs755931388 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047959 | TGTGAGACCCTGTCT[-/C]AAAAAAAAAAAAAAA | 114088 |
rs755967162 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074580 | TCATTTTAGGAAGTA[A/T]ATAGTCCAAAATGGC | 114088 |
rs755980340 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983582 | TTGTTGGGTAAAAAA[A/C]TGCCCCTCTGCTCTT | 114088 |
rs755997414 | snp | C/T | 0.00018388 | 0.00958678 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009036 | TCAAGCACCAGCATC[C/T]ACTCAGGATGTTGCT | 114088 |
rs756048157 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023963 | TTTATATAATAATCA[A/C]CTGGTAGGCATTTAG | 114088 |
rs756072713 | snp | A/G | 1.80699e-05 | 0.00300577 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094560 | TGACACTGGGGGCAG[A/G]TGATACAGGAGTTGC | 114088 |
rs756124111 | snp | A/T | 1.64808e-05 | 0.00287057 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009161 | CAAAGTCCGTGGTCA[A/T]CCTTGGAGTGAGTGT | 114088 |
rs756143610 | snp | C/T | 0.000117927 | 0.00767786 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094814 | GGGGGATTCAGACTC[C/T]GGGGTCTGCACCAGG | 114088 |
rs756205752 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068066 | CTTATTAAAACACAG[G/T]TTGCTGGACCCCCAA | 114088 |
rs756220011 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079978 | CAAAAAAGCTAGCAA[A/G]TAGTGCAAATGAATG | 114088 |
rs756237632 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000399 | GGGGTGATAATTAGG[C/T]ATTGTCCACATAGCT | 114088 |
rs756266130 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037639 | TTACAAATTTCATTT[A/G]GAAATTATTAATTAA | 114088 |
rs756297775 | in-del | -/AGTCTTACCTCGTA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051483 | CGGGTGAGGGCAGGC[-/AGTCTTACCTCGTA]GGCCTTTGCTACATG | 114088 |
rs756355038 | snp | A/G | 3.42865e-05 | 0.0041403 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010544 | GATGGCAGAGGGTAG[A/G]AGAGAAGCAAACTGG | 114088 |
rs756399511 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018543 | TGGGATCATAACAGG[C/T]AATACATGGTAAATA | 114088 |
rs756406420 | snp | A/G | 3.29544e-05 | 0.00405908 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982021 | CACCCGGTCATCATA[A/G]CTACTACAGGTCACT | 114088 |
rs756409559 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060628 | CCTGCCACCACGCCC[A/G]GCTAATTTTTTTGTA | 114088 |
rs756440944 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049059 | GTGTAAGCACCGTTA[C/T]GTGGTTTTCTTGTTC | 114088 |
rs756451206 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021546 | GAAGTCCTTCTGAAC[A/C]ACCTTCATGTCCCTG | 114088 |
rs756497443 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060109 | CAGAATTTATAATGG[A/G]CTTTCTAGCTTTCTG | 114088 |
rs756527351 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078769 | TGAAGGAGATGTAAG[C/T]CCAATAATTCAACGG | 114088 |
rs756561904 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039022 | TTTTCTCAAAGGCAC[A/G]GGGTCATTAGAAATG | 114088 |
rs756567455 | snp | A/G/T | 5.73809e-05 | 0.00535609 | intron-variant, synonymous-codon, stop-gained | TRIM9 | GRCh38.p7 | 14:50998020 | TGCCACGCAGTTCTC[A/G/T]CTCTGAGGGATACTG | 114088 |
rs756596648 | snp | A/G/T | 4.67344e-05 | 0.00483374 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979241 | AAGTTGCCAGTGCTG[A/G/T]TCCCTTTCTCTCCTC | 114088 |
rs756609736 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999601 | ACATTCAGGAAAAGG[C/G]GGCCTTGAGAGGCTT | 114088 |
rs756626962 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078250 | TGTAGTGGGTATATT[G/T]TGCCACTGATAAATA | 114088 |
rs756634548 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004356 | ATTTTCCAGTAGCAG[C/G]TTCTTATACCAATGT | 114088 |
rs756636977 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091601 | TATTAAGTAAATAAG[G/T]TGGGGGAGTAATGTT | 114088 |
rs756642057 | snp | A/G | 3.50214e-05 | 0.00418443 | missense, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977335 | AGTCGGGGACTGGGA[A/G]CCCGGTGTGCAGCGT | 114088 |
rs756643145 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049908 | ATGGCTCTGGTATGT[G/T]TAAAAGGTGACAAAA | 114088 |
rs756688493 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990425 | AGTTGGCAGGAGACT[C/T]AACCATAAGAAAAAT | 114088 |
rs756741644 | snp | A/G | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095382 | GGAGGAGTTAGGCGG[A/G]ATGATTCATCCTCGC | 114088 |
rs756763601 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054869 | GAGTCTGGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 114088 |
rs756763726 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015825 | CTTTTTCCTATAGTA[C/G]TCTCTCTCATCATAG | 114088 |
rs756777236 | in-del | -/GT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030588 | GAGTGTGCATATGGT[-/GT]GTGTGTGTGTATGAG | 114088 |
rs756801864 | snp | A/G | 3.29587e-05 | 0.00405934 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025344 | GACAGTCCGTTCAGC[A/G]CCTGGGAGAGCTGGC | 114088 |
rs756828048 | snp | A/C | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976313 | ATTTTTAGCATCATT[A/C]TAGGAAGCCTGAAAG | 114088 |
rs756834283 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003841 | CGTTTTCCTTATTTA[A/C]CCCCAGTGATGTTGT | 114088 |
rs756849629 | snp | A/G | 3.46783e-05 | 0.00416388 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094090 | TCGGAGACGCAGGGA[A/G]TTAGGAGTGGGTTTT | 114088 |
rs756852017 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065570 | AGAAGTAAGGACACA[C/T]ATTTTTGCCCTCCTT | 114088 |
rs756906479 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992998 | TTCCCTCCCAGTTAG[C/G]ACAGGCAGGGCTGGA | 114088 |
rs756921277 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031327 | AATTCCTAAGATGAC[A/C]CCAGCCTCCCTTAAG | 114088 |
rs757003694 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036742 | CCATGCATACAGAGG[G/T]CTGACTGTATATCCT | 114088 |
rs757014729 | snp | G/T | 1.66048e-05 | 0.00288134 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998224 | GGACAGCACTTAGCC[G/T]GCCCCCTTCTGAGGG | 114088 |
rs757023610 | in-del | -/AAAAACAAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068341 | ACCAAAAACAAAAAC[-/AAAAACAAA]AACAAAAAACAAACC | 114088 |
rs757052786 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977160 | GTGTAAAGACTGCAG[A/G]GGACCAGCTTTTCTC | 114088 |
rs757053120 | snp | A/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997138 | TAAAATGACACCCCA[A/T]AGTGTCAGAATGCTT | 114088 |
rs757079784 | snp | G/T | 5.58321e-05 | 0.00528327 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094606 | GGGCCGGTGACAAGT[G/T]GGTGGCCGGTGGCGG | 114088 |
rs757153531 | snp | C/T | 1.65042e-05 | 0.0028726 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009224 | CTCTTCTTATGAGGG[C/T]GTCAGAAATCTAATC | 114088 |
rs757163838 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986198 | TGCTATTATGTCCCC[A/G]TGCACGGTTCCCCAA | 114088 |
rs757176875 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985063 | AGAAACCTTTGGAAA[C/T]ATGAAATGTGCATCA | 114088 |
rs757256204 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064916 | GAAATCATTATAAAT[C/T]ATAAATAAAGCTTAA | 114088 |
rs757259669 | snp | C/T | 6.65059e-05 | 0.00576616 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010350 | TGTCCTATGGGACAT[C/T]TAGAATCTGACGCAG | 114088 |
rs757270399 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981871 | TGCCCAAGCTTTGTC[A/G]TCTTTTCCTAACATC | 114088 |
rs757293734 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086217 | GAACAGCAGTTAAAC[A/C]TGTGAGTTGTAGAGT | 114088 |
rs757303395 | snp | C/T | 1.6489e-05 | 0.00287128 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982049 | ACTGTCAGGTTGTCA[C/T]TGGAGAGGATGATGT | 114088 |
rs757333221 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992429 | CGGAAAAAAAAAAAA[-/G]CCAGGTGTGGTGGCA | 114088 |
rs757363185 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018593 | AAAGAATGATAATTA[C/T]TCTAACAAAACTCAT | 114088 |
rs757409963 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020011 | TTCCTAGTTTTTTGG[A/T]TTGCTCAAGGAGAGA | 114088 |
rs757411901 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980513 | CCTCTTGCTACTTCA[C/T]AGGTTTAACAATGAA | 114088 |
rs757429788 | snp | A/C | 1.80775e-05 | 0.00300639 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982143 | GTTATTAAGACAGAC[A/C]CAACAAGCTCAGCAC | 114088 |
rs757490493 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058765 | CAGCTACATATGGTG[G/T]GACTCACTATCACAC | 114088 |
rs757528446 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979706 | CATAAATTTTAATAC[C/T]GCAGATATACTGTAT | 114088 |
rs757531805 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092352 | TGGATCACATTCAAC[C/T]GGGTTAAGGAGTTGA | 114088 |
rs757535792 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008138 | GGGGTTTCCAGAGAT[C/T]AGAGTTGGTGGAGGG | 114088 |
rs757553642 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050441 | CGCCTTCCACCATGA[C/T]TGTGAGGCCTCCCCA | 114088 |
rs757571354 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039097 | CAGGCCTTTACAACA[C/T]CGATGCAAAGATTGG | 114088 |
rs757647619 | in-del | -/A | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097386 | CCCTGTAATTACAAG[-/A]AGAGGTAGGCACAAT | 114088 |
rs757653098 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091608 | TAAATAAGGTGGGGG[A/G]GTAATGTTTGTTGTT | 114088 |
rs757669126 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028773 | CAGCTGAAGCCCTGA[A/T]CTCCAGTCAAGTTGT | 114088 |
rs757694181 | snp | C/T | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983364 | AGTAAAAGATAATTA[C/T]AATAGGTATACTTGC | 114088 |
rs757696636 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989367 | GAAGGCACACACTAC[C/T]TCCTCACCTCCCCTT | 114088 |
rs757711344 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080279 | ATTCATGTTATAGTA[G/T]AGACATATATAACTT | 114088 |
rs757759036 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040535 | GTGACTGGAGCCCTG[A/G]AGTGAGGGATTGGAC | 114088 |
rs757798486 | snp | A/G | 3.30764e-05 | 0.00406659 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022786 | TCCATCATGCCCCTC[A/G]GGAGCCTGGCTTGTT | 114088 |
rs757868201 | snp | C/G | 1.66396e-05 | 0.00288436 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094126 | GACTCACCTTATGTA[C/G]TTTCCACATGGCCCC | 114088 |
rs757887090 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081512 | ATGTACTTCAGTGAC[C/T]CCAATTTACCGACAT | 114088 |
rs757917407 | snp | C/G | 1.65037e-05 | 0.00287256 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094243 | TGTGGTTCTCCAGCT[C/G]GTGGTCTGTGCAGGT | 114088 |
rs757929372 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045714 | GTTTGTCAGAAAAAG[A/G]AAATTCAATGGCCCC | 114088 |
rs757943213 | snp | C/T | 1.6654e-05 | 0.00288561 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998232 | CTTAGCCTGCCCCCT[C/T]CTGAGGGGCGAGGGA | 114088 |
rs757956242 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005479 | ACTCATGAATCTTGG[A/G]ATTCTTTGTGTACTT | 114088 |
rs757978822 | in-del | -/GTGA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060957 | CTAACATTTGCTACT[-/GTGA]GTCTTTTTCATTTTA | 114088 |
rs757982501 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047838 | TTCATTCACATTAAA[A/T]GAACAATCCATTTTT | 114088 |
rs757983876 | snp | A/G | 1.64811e-05 | 0.00287059 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000754 | CCGTGGACAGAGGTG[A/G]CTGTTTCCAGGACAA | 114088 |
rs758000442 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995452 | AATAAATAGACAGAT[A/G]AATTTGCTTTCGAAG | 114088 |
rs758004356 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994242 | AAGACCACATCTCTA[C/T]AAAAAATTTAAAAAA | 114088 |
rs758008074 | snp | A/G | 1.64833e-05 | 0.00287078 | intron-variant, synonymous-codon | TRIM9 | GRCh38.p7 | 14:50979372 | GCTGTTTAACCTCAG[A/G]GGCAGGGTGCTTACC | 114088 |
rs758053628 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092611 | CTTCCAACCATCCTG[-/A]ATCCCTGCCCTGCAC | 114088 |
rs758074051 | in-del | -/C | 2.03172e-05 | 0.00318719 | frameshift-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094691 | GGGGGCGCTGGCGAA[-/C]CCCCCGTAGGAGCCA | 114088 |
rs758077920 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026303 | GGAGGGGAAGGAGCT[C/T]GGTTCTGATGGCATC | 114088 |
rs758089035 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060678 | TTCGCCGTGTTAGCC[A/G]GGATGGTCTCGATCT | 114088 |
rs758110934 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074175 | TGTAATCCCAGCACT[A/T]TAGGAGGCTGAGACA | 114088 |
rs758136708 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033538 | TCGTTCAGAACAATT[C/T]GCTCTGGTCCCATTT | 114088 |
rs758158105 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066396 | CTTCCCAGCAGTCCT[G/T]GACACAGAGAACATT | 114088 |
rs758161802 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065079 | CAATAATATTAACAA[C/T]ATAAAAAATAGCTCA | 114088 |
rs758256934 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988882 | TTAGAGGGAAGAAAC[-/TT]AATATCATCAGAGGA | 114088 |
rs758291706 | snp | G/T | 4.94539e-05 | 0.00497238 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981906 | CCTTCATCACGTCCA[G/T]GCGAGCCACACCAAA | 114088 |
rs758306971 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083528 | GATTACAGGTGTGAG[A/G]TACCATGCCCAGCAG | 114088 |
rs758330241 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016924 | TACTTTTAAGATGCA[A/G]GTTTGAAGTGTTTGT | 114088 |
rs758344911 | snp | C/G | 1.6476e-05 | 0.00287014 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982011 | TCCCTAGCACCACCC[C/G]GTCATCATAGCTACT | 114088 |
rs758370732 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027395 | GTGATCCACCCACCT[C/T]GACCTCCCAAAGTGC | 114088 |
rs758377619 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022573 | TCCCATGAAGGCAAG[A/G]ATTTTGATTTCTTTA | 114088 |
rs758386244 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044285 | CAAATTGTTGCAGGG[C/G]CTACCAACTGCCTTC | 114088 |
rs758438584 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047682 | GTACAGGAAAGAAAC[A/G]CATATAACAATCTGT | 114088 |
rs758440890 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981478 | TTGCCCAAAAGTGCT[G/T]TTCTGTTAAGTTGTA | 114088 |
rs758456465 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036119 | GTTTCTTTTTGCCAT[-/G]CCCCGAGGCAAAAAG | 114088 |
rs758458813 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020225 | TCTTTTCTCACAAAT[C/T]TGAGTAGCAACAAGA | 114088 |
rs758486239 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087663 | AAGGTTAAAAATTGA[C/T]CCAAAATGTCAATAT | 114088 |
rs758496472 | snp | C/T | 0.000182365 | 0.00954722 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985972 | CGGTGCATTGAGAGA[C/T]TGTAAAGAGGAATGC | 114088 |
rs758517641 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037758 | CTCCTGTATCTAAGA[C/T]TAAAGTCACAAGTTG | 114088 |
rs758643243 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075766 | CAAGGCGGGGAGTGG[G/T]TCTGATCGATCTGAA | 114088 |
rs758668978 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076923 | CCTGACCCTATACTG[A/C]CCAATGCCATTTGGG | 114088 |
rs758677853 | snp | C/T | 1.68593e-05 | 0.00290334 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094424 | TTCCTTGGGCGCCTT[C/T]TCGCAGAGCTGGCAC | 114088 |
rs758680524 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082207 | GGGTTTTAGGAGCTC[G/T]GAGCCAGGAACCACG | 114088 |
rs758722051 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041491 | ATGTTTCAATCTCAG[C/G]TGTAGGGAATAGGTT | 114088 |
rs758796672 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081683 | TTCTTTCTGACTTGA[C/T]TGCAACCTTGGATCA | 114088 |
rs758803353 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019428 | CAGTTTCCCTCAAAC[A/G]TGTCCACATCTGCAT | 114088 |
rs758819520 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975548 | ATAAACAGGATAGCA[C/G]CCATTCCATAAATTA | 114088 |
rs758823216 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979444 | CTCCACGTTATCAAA[C/T]GCTATGGGACCTTGT | 114088 |
rs758826829 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069749 | ACTGGACTATAACTG[A/G]CCCCATATTCCTTGG | 114088 |
rs758835372 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002705 | TTAGAAAACAGGTTC[C/T]ATGGCAGATAACCTA | 114088 |
rs758850165 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003544 | TGTGTAGACATAGGT[A/G]TAATTAAAAAAGTAA | 114088 |
rs758873475 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030831 | GCTCCATTAAACTGC[C/T]GCTTATTGTTAATTG | 114088 |
rs758874406 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040832 | AAATGACCCTTAACT[C/T]TTCCGCTTACTACCA | 114088 |
rs758986839 | snp | C/G | 1.75625e-05 | 0.00296327 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094523 | GCCGCGGAGCCCCCG[C/G]TCATCCAGGATGAGG | 114088 |
rs758988976 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072555 | TTCTATTGAGAAAAT[A/G]GAAAGGAAAAAGAAT | 114088 |
rs759002488 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020266 | AGGGAAAAGGCAGGG[A/G]GAGAGGAGAGCGAGC | 114088 |
rs759016180 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058305 | AGTTACTCAGGTGAT[A/G]TGAGGCTCACATCTA | 114088 |
rs759043775 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047348 | ACAGCATCTGGGCCA[C/T]GGCATTCATTTCATC | 114088 |
rs759099736 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088475 | AATGCTGACCTAGAG[A/T]ATAGATAAAACAAAA | 114088 |
rs759109313 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037205 | TCTAAATAACTCCGA[C/G]ATCAAATAGGAAATT | 114088 |
rs759120947 | snp | C/T | 1.64833e-05 | 0.00287078 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009131 | GCAGCAGAGGGCTGT[C/T]GTCCAGACTCAAGTC | 114088 |
rs759121637 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047945 | AACCTGGGCGATACT[A/G]TGAGACCCTGTCTCA | 114088 |
rs759125163 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019856 | CCCAGCCTCTATGAC[A/G]CAGAACCTGGGCTCT | 114088 |
rs759126335 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980347 | GCCATTAAAAATGGA[C/T]GATCAGATTTGTCTT | 114088 |
rs759132730 | snp | A/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997881 | GATCACATCCACATA[A/C]CATAGGCTCTCTAAA | 114088 |
rs759161962 | snp | C/T | 4.01711e-05 | 0.00448151 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094698 | CTGGCGAACCCCCCG[C/T]AGGAGCCATAGCCGC | 114088 |
rs759208655 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008521 | AAAATATTTTCAGCC[C/T]CCACCCAGAATCTCA | 114088 |
rs759213385 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984023 | AGGGATGGTAGGAGT[-/G]GGTGTGGTCTCAGAG | 114088 |
rs759217020 | in-del | -/CA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047959 | TGTGAGACCCTGTCT[-/CA]AAAAAAAAAAAAAAT | 114088 |
rs759222470 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003071 | GAGAAGGACACAGAA[A/G]ACATAATGCCTTCTA | 114088 |
rs759241180 | snp | A/G | 1.66164e-05 | 0.00288235 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009266 | ACCACAGCCTAAGAA[A/G]TACACCACCACACTT | 114088 |
rs759283491 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037269 | AGCCACTTTATACAA[A/G]TGTATTGCTTTTAAA | 114088 |
rs759330210 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028569 | CCAGAACAATGAAGA[C/T]GCAAATATGTAGTAT | 114088 |
rs759343173 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991314 | AAAATGCAAGAAATT[C/T]CCTGGGATATCATGC | 114088 |
rs759353802 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060188 | AACAGCATTTTCGTC[A/T]TATTATTTATGTGGT | 114088 |
rs759371432 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046382 | GAATAAAATCAGTGT[A/G]CTTTATCACTGTCAG | 114088 |
rs759403634 | snp | C/T | 1.64863e-05 | 0.00287104 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022978 | TAACAGAGCACATTT[C/T]TCAACTGCAAGCTGC | 114088 |
rs759403980 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081247 | TAAGCACATGAAAAG[A/T]TTCTCAACATCACTA | 114088 |
rs759443966 | in-del | -/AT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043836 | CCTGTTTGGTTTAAC[-/AT]TTTTATTTTAATGCA | 114088 |
rs759531763 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070452 | CTTGGTGACTTAATA[G/T]AACATAACTACAGGT | 114088 |
rs759557362 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073958 | ACTGACTTCCAAACA[C/T]CAAGGTCAGCAACCT | 114088 |
rs759583406 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092539 | GAGGCCTGGACACTA[G/T]CTTCACTGCTCCATC | 114088 |
rs759618741 | snp | C/T | 3.29707e-05 | 0.00406008 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000706 | GACCACCGTTGCCAT[C/T]ATCCAGCTCCAGAAT | 114088 |
rs759664148 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022392 | AGCATGAAGGCCCCA[A/C]CAGAAGCCAACACCA | 114088 |
rs759683617 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060611 | AGCTGGAACTACAGG[C/T]GCCTGCCACCACGCC | 114088 |
rs759684317 | snp | C/T | 3.36902e-05 | 0.00410414 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979337 | GCCCTGGGCAGCCTT[C/T]GAACCGGTAGCCAGC | 114088 |
rs759690144 | snp | C/T | 1.64762e-05 | 0.00287016 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998137 | CGTTGTATGTGCTGT[C/T]GAAGTGAAGACCATC | 114088 |
rs759707052 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011451 | CCTATCTCAGTCTCC[A/T]AGTAGCTGGGACTAC | 114088 |
rs759719270 | snp | C/G | 1.75293e-05 | 0.00296046 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094941 | TCCATCTCCTCCATG[C/G]GGACCGGTCTGGGAG | 114088 |
rs759720055 | snp | C/T | 1.64852e-05 | 0.00287094 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094177 | TGGAGTGTTTGCCCT[C/T]CTCCAAGCACTGGTA | 114088 |
rs759722710 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079807 | GCTAGATGAAAAGAC[C/T]GTACACAGGTCAGAA | 114088 |
rs759728351 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982534 | AACACATGGAGTGAA[A/T]TCAGGAAATATCCCT | 114088 |
rs759782096 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043750 | ATGAAACTGAGAAGA[C/G]CTGGTAGCCGAGATA | 114088 |
rs759791877 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977397 | GGCATCGTGCATCCC[C/T]CTGTCCCTTTACACA | 114088 |
rs759839709 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088415 | CAGAATGGAGAGTCT[C/T]AAACTTATTTAACTA | 114088 |
rs759848629 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091892 | TAATTTCTATTGCCA[A/G]TAAAACAAATGATTT | 114088 |
rs759858057 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016427 | TCTAATGCCTGATGA[C/T]CTGAGGTGGAACAGT | 114088 |
rs759860492 | snp | C/T | 8.23621e-05 | 0.00641672 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981836 | TGCATGAACCAGCTC[C/T]GGTTATTGTCCACAT | 114088 |
rs759883129 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977709 | AAATCCATGGATAGA[A/G]GACAGATTCGCAGAG | 114088 |
rs759892513 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050311 | GGGCAGTTTTCCCCA[C/T]ACTGTTCTCGTGGTA | 114088 |
rs759933656 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001228 | AAGCTGTGCTAATAA[-/T]TTTTTTTTTTTTTTT | 114088 |
rs759983456 | snp | C/T | 1.64735e-05 | 0.00286993 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981952 | GTTGTCATAGCGATC[C/T]ACCGTGAGCTCCCAG | 114088 |
rs760051589 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045111 | GAGCTGTTCAAGACT[C/G]ATTGGTGGGATTGCT | 114088 |
rs760052634 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032400 | AGGGAATATCAGCTG[C/T]TGATAGATTACCCTA | 114088 |
rs760064129 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993889 | GCAGCTCAGTTTCCC[A/G]TAAGTAGAGAAAGAT | 114088 |
rs760075068 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085361 | CCAAAGCCAGCTCTT[G/T]AAAAGGGACAGTTTC | 114088 |
rs760126607 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073331 | TGCTTACATTTATGC[A/G]CCAAAAGACAGGTGC | 114088 |
rs760131845 | snp | A/G | 3.33167e-05 | 0.00408133 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010336 | AGCATCCTAGACTAT[A/G]TCCTATGGGACATTT | 114088 |
rs760141465 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005372 | GGATTAACAGCCAAT[C/G]GTCTATGTGCTAAAA | 114088 |
rs760142262 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980343 | AAATGCCATTAAAAA[C/T]GGACGATCAGATTTG | 114088 |
rs760150933 | snp | A/G | 0.000175793 | 0.00937367 | intron-variant | TRIM9 | GRCh38.p7 | 14:50985940 | CAAGGGGAAAGGTCT[A/G]AGGAGCTCAGCTCAC | 114088 |
rs760166525 | in-del | -/C | 1.85555e-05 | 0.00304588 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982156 | ACCCAACAAGCTCAG[-/C]ACCATAACATACTCC | 114088 |
rs760168388 | snp | A/G | 2.06836e-05 | 0.0032158 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025398 | CATGGAGCTGTAATC[A/G]CAGGATACACCAACA | 114088 |
rs760267297 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095225 | GCAAGAGATCGAAGC[C/T]CTCATTGGCCACCAG | 114088 |
rs760275667 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987700 | AAAAATTCAAAATAC[A/G]ACACCCAAGCACCAC | 114088 |
rs760284946 | snp | C/T | 4.26321e-05 | 0.00461673 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094883 | GGGCAGGATGATGGG[C/T]TCCCGATAGAAGGAG | 114088 |
rs760288999 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076643 | TAACATGTGCCAAAA[A/C]CTCACATTAATTAGG | 114088 |
rs760310829 | snp | C/T | 6.6433e-05 | 0.00576299 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010494 | TCTGATCTCGAACCA[C/T]CTAGGATTAAAAAAA | 114088 |
rs760322167 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071167 | GGATCACCTGAGGTC[A/G]GGAGTTCAAAACCAG | 114088 |
rs760322582 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038368 | TGTTGTTTTAAGTTG[C/T]TAAGTTTTTTGTACT | 114088 |
rs760331338 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033897 | TTTATATTATGCATA[-/TT]CTCTTTATATTATAT | 114088 |
rs760352790 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992368 | GGATCGCTTGAGGCC[A/G]GGAGTTTGAGACCGG | 114088 |
rs760360077 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015749 | GGTGTCAAGTGATCC[C/T]CCAGCCTTGGCCCCC | 114088 |
rs760378012 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026057 | AGGTAGGTACTTGCT[C/T]TTCCAGCCTCCTCGT | 114088 |
rs760381941 | snp | A/T | 1.64735e-05 | 0.00286993 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981957 | CATAGCGATCTACCG[A/T]GAGCTCCCAGTAGTG | 114088 |
rs760386482 | in-del | -/C | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975444 | TCTACCACGGCCCAG[-/C]CATTGAGTCTCATTG | 114088 |
rs760437714 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033464 | ACTTTTGTCATACCA[C/T]GTCTTGACTGAGGGT | 114088 |
rs760449681 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058708 | TCAGCTGTCTTTTAC[A/G]TGAAAGAAATAAATT | 114088 |
rs760466818 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065984 | AAATACAGGGCCTGT[G/T]CCATCAACTTCTTTA | 114088 |
rs760469397 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008936 | GAAAGGTAGGTCACA[C/T]ATTTATAAGGATACA | 114088 |
rs760496407 | snp | A/C | 2.91422e-05 | 0.0038171 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997987 | GGGGTTACCTCCGGG[A/C]TTGCCAGCCACTTTA | 114088 |
rs760558741 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092811 | ATACAAAAAATAACA[C/T]AATTAAAATATATAG | 114088 |
rs760577326 | snp | A/T | 1.93654e-05 | 0.00311164 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094752 | ATCTTGTCCAGGTCC[A/T]GATAGTCATAGTCGG | 114088 |
rs760588629 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991472 | ACTTTGTCCTGGAAA[A/T]GCATATTCTTCTAAC | 114088 |
rs760590041 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059713 | TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG | 114088 |
rs760591564 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030544 | AATGGAAGCACACAG[A/T]ATAGGGACAAAGGAT | 114088 |
rs760645783 | snp | A/G | 0.000285893 | 0.0119526 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977282 | AGCTGGCGCCTCCAC[A/G]GCACATCCTTAGGCT | 114088 |
rs760659835 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047396 | GAGCTCCTTGAGGAT[A/G]AGGACAGGTGTGTGG | 114088 |
rs760705415 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024475 | AAATATGAACTTAGG[C/T]AATTTACTGGAGGCC | 114088 |
rs760726037 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019971 | GATTATAAAGACTGC[A/G]TAAGTACACACTCAC | 114088 |
rs760740682 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074987 | TCTTCACAAAGGCAC[A/G]AGCAACAGGCAGCGG | 114088 |
rs760782219 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013138 | CTGTGTTCTCTCCCA[A/G]GAGTTTATAGTTTTA | 114088 |
rs760791033 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979426 | CGCAGGGAAGAAGAG[A/G]CCCTCCACGTTATCA | 114088 |
rs760815933 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041216 | GTTAGAATCTAAGAT[C/T]TGACTCCCATGAAAA | 114088 |
rs760816313 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093500 | CCATGGCGACCGCTG[A/G]CTGCCCTCTCCGCTC | 114088 |
rs760829055 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081823 | TGGCAGAGACGCATG[A/G]AGTAAGGTACTAGGG | 114088 |
rs760833321 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003238 | TTACTACGGAAGATA[A/G]ATATAACAAGTTTTG | 114088 |
rs760852400 | snp | A/G | 6.58913e-05 | 0.00573945 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022865 | ATGCTCCTTGTTGAC[A/G]CGGGCCAGCAGCTGG | 114088 |
rs760901869 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984107 | TGGATACCTGTACCC[C/G]ATGAGAAATTACATT | 114088 |
rs760945339 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042256 | ACCCAGCAGAAGATA[A/G]TTATGGCCAAATCTG | 114088 |
rs760976752 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085551 | TTCTGAACTGGAATA[C/T]GCATATTTTCTTTTA | 114088 |
rs761000307 | in-del | -/GAAAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035042 | TATAACACATTAAGT[-/GAAAA]GAAAAGAACAGATTT | 114088 |
rs761008149 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006117 | AGTAAACAGATATTT[C/T]AGTTATGATTTTGAG | 114088 |
rs761062586 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070437 | CATTAATTCAGTGTA[C/G]TTGGTGACTTAATAG | 114088 |
rs761070154 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045995 | AAACGAACCAGTGCA[A/C]CACACATTGACGTAA | 114088 |
rs761092826 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995333 | ATTTCTCTAAGGCTT[A/G]TTTCCTTTTCTAGCT | 114088 |
rs761149607 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027491 | TGCTCACACAAACAC[C/T]TGCTGACTGGAGGGA | 114088 |
rs761194799 | snp | C/T | 6.59272e-05 | 0.00574101 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094204 | GGTAGCACACGGGCA[C/T]CTTGCATTGCACGCA | 114088 |
rs761234283 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062067 | CTGATTCTTTCTGCC[A/G]CTATATCCAGTCTGT | 114088 |
rs761236259 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085552 | TCTGAACTGGAATAC[A/G]CATATTTTCTTTTAA | 114088 |
rs761247217 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035024 | AGTCATATGGGAAAA[C/T]ATTTATAACACATTA | 114088 |
rs761284325 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987718 | ACCCAAGCACCACAA[A/C]CTGGCATGGGTTTCT | 114088 |
rs761319285 | snp | C/T | 1.64982e-05 | 0.00287208 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000733 | GAATGTATCCATCGG[C/T]GGGCACCGTGGACAG | 114088 |
rs761357209 | snp | C/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096721 | ATAAATGTGACGTGA[C/T]TTATTTTTAAGCTGG | 114088 |
rs761410506 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079383 | TTTACTTCCTGCCCT[C/T]AATGTAAGTAGAACT | 114088 |
rs761442442 | snp | C/T | 1.64825e-05 | 0.00287071 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022825 | GCTCTTCCCATGATG[C/T]AGCACTCACCTTCAG | 114088 |
rs761459460 | in-del | -/CTGACCTA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079313 | ATTGAGTAATAATCT[-/CTGACCTA]CTAATTCACTCCTTC | 114088 |
rs761467798 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005402 | AAGGCTTGGTGAACT[A/G]TTAGGTCATTGTTTC | 114088 |
rs761483517 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028284 | AGATAAAGATCTAGA[A/G]ATCATTCTCTTAAGC | 114088 |
rs761505960 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068584 | TACAGATGACAAAAA[C/T]GGGGCTCAGAAAGGT | 114088 |
rs761507387 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036182 | CCATGTTGATGAGCC[A/G]GCCCACGGCACAAAA | 114088 |
rs761529971 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057674 | AGAAGCCATGAAAAT[A/C]ATGTTTTATTTTCTT | 114088 |
rs761553650 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016681 | TATCTGCAGGGAATC[A/G]TGGAATCAATCCCCC | 114088 |
rs761555220 | snp | G/T | 1.89432e-05 | 0.00307753 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977389 | TCCTGAGAGGCATCG[G/T]GCATCCCCCTGTCCC | 114088 |
rs761573492 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982253 | GGGCAGACAGGGGCA[C/T]GTCCTGGGAGTTGGT | 114088 |
rs761584746 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999140 | CATTTTTAACAAGTT[C/T]CCAGGTGAAACCAAT | 114088 |
rs761618052 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056020 | AATGTATAAATTCAG[A/G]TAAGTATGTCCAAAA | 114088 |
rs761663322 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981378 | TTCACATATTTCATT[C/T]AATCTTCAGAAGATT | 114088 |
rs761670768 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049434 | ACAGGGCTGCCACGA[C/T]TGCTCAGCACAACTC | 114088 |
rs761715812 | snp | C/T | 1.93347e-05 | 0.00310918 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094761 | AGGTCCAGATAGTCA[C/T]AGTCGGAGACCCCGG | 114088 |
rs761716659 | snp | A/G/T | 1.80644e-05 | 0.00300531 | intron-variant, synonymous-codon | TRIM9 | GRCh38.p7 | 14:50979321 | TCGGTTGGATTGAAC[A/G/T]GCCCTGGGCAGCCTT | 114088 |
rs761732952 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038470 | TTGGCGGTGGTCGGA[C/T]TGCTTCACCTGATAT | 114088 |
rs761747714 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077456 | GGAGTGCAGTGGCAC[A/G]ATCTCAGCTCACTGC | 114088 |
rs761749319 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037700 | AAGACACAGAGACTC[C/T]TTGGCTCTTTAAAAA | 114088 |
rs761752632 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021031 | TTAGCGGGGAAAACT[G/T]TTCAGTTTCATTTCC | 114088 |
rs761779536 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053902 | AGAAATATATTATGG[C/G]TAAGAGTGAATCTAC | 114088 |
rs761801607 | snp | A/G | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094626 | GCCGGTGGCGGCATA[A/G]CCGGGGGAAACACGC | 114088 |
rs761842603 | snp | A/C | 4.82172e-05 | 0.00490981 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094905 | TAGAAGGAGCCGCAC[A/C]CGGGGCATTTCAACT | 114088 |
rs761891928 | snp | A/C | 5.02871e-05 | 0.00501408 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010512 | AGGATTAAAAAAAAA[A/C]CAACAGAACAGTCCA | 114088 |
rs761928413 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070710 | AACAGGGATTGACTG[C/T]ATGTCTTTTACAGAA | 114088 |
rs761928596 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083015 | GTAAAATGAGAATAG[C/T]AATGGTTCTTGCCTC | 114088 |
rs761930329 | in-del | -/ACACACACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080439 | TGAGTTTTATTGAAC[-/ACACACACAC]ACACACACACACACA | 114088 |
rs761955079 | snp | A/G | 1.65255e-05 | 0.00287445 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979534 | TGTGGCCCCTTTTGT[A/G]ATCCCTCCCTCAGTT | 114088 |
rs761983294 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095656 | CAGTGGGGCTTTTCT[C/T]CTTCTCCGTGAATCC | 114088 |
rs761984865 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062429 | TACCAGTTTCACTCA[C/T]GGTGGAGTAGCCTTT | 114088 |
rs762021017 | snp | A/G | 1.64904e-05 | 0.00287139 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022989 | ATTTCTCAACTGCAA[A/G]CTGCTGGGTGCCTCA | 114088 |
rs762027076 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043501 | CTTAAGCAGTTCTAT[C/T]TACAGCCTATCTGTG | 114088 |
rs762039885 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042767 | AACTGGTGTCCCTTC[C/T]TCATGAGCTTTGCCA | 114088 |
rs762052668 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984450 | TGGGATGAATTCACA[C/T]GCAAAAGAATCGTTT | 114088 |
rs762076076 | snp | A/C/T | 8.24482e-05 | 0.00642014 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025244 | CGGCGGGTTTCCTTG[A/C/T]GTCCCAGGTAACACC | 114088 |
rs762076866 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059917 | TTTAGAATATTGGCT[A/G]CTACCACGGCCCTAA | 114088 |
rs762080810 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032102 | TACCTCTTTTTAAAT[A/C]ATAATTTAAGTCTAA | 114088 |
rs762088881 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022124 | TATTTTACTTACTTA[C/T]TGCTATGGTTTGAAT | 114088 |
rs762090145 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991689 | AATGCTGCTTCATAG[C/T]ATTTTCTGAAACAAC | 114088 |
rs762107813 | snp | A/G | 1.69398e-05 | 0.00291026 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094360 | GGTGGCAGCGCAGGC[A/G]GCACGGATCGCAGTA | 114088 |
rs762136017 | in-del | -/C | 1.93969e-05 | 0.00311418 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977401 | CGTGCATCCCCCTGT[-/C]CCCTTTACACAGTGT | 114088 |
rs762163337 | snp | C/G | 1.648e-05 | 0.0028705 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000827 | GATAGGGGTTGCTGG[C/G]ACTGGAGAGGAAGCT | 114088 |
rs762177612 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028855 | AGTTGTTCAAGCCTG[A/C]AGGAGAGAAACAAAG | 114088 |
rs762315006 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023534 | GATCACCCTGCCATA[A/C]AAATCAGATATGACC | 114088 |
rs762323429 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043835 | CCTGTTTGGTTTAAC[-/A]ATTTTTATTTTAATG | 114088 |
rs762331894 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985472 | GTTGGTGTGTTTTTA[C/T]TTTTATTGTACTTTG | 114088 |
rs762367115 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051469 | AATTTGGGACAGGTC[A/G]GGTGAGGGCAGGCAG | 114088 |
rs762370246 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007802 | ACACATATTAAACCA[-/AA]AAAAAAAAAAAAAAG | 114088 |
rs762372673 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014600 | AGATTTCCCACATTA[C/T]AGAAATCAGGCAGAT | 114088 |
rs762392143 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981669 | AGGCTCATAGATTGC[A/C]TGTGCTACTTAATGT | 114088 |
rs762396313 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090842 | CCGCAAGAGATCTGA[C/T]CGCCTCGGCCTCCCA | 114088 |
rs762433231 | snp | A/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978194 | CAATGTTACTGCACA[A/T]ACTGAAACACAACAA | 114088 |
rs762440134 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093520 | CCTCTCCGCTCTGTC[C/T]TTTGAGCACGTGGCA | 114088 |
rs762482143 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047288 | CCTCTGAAACTCTGT[C/T]CTTGACTTGCCCCAC | 114088 |
rs762503780 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018265 | TTTTTTGTGAGCTGG[A/G]ATGGCCTGCCTGCCT | 114088 |
rs762526659 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070712 | CAGGGATTGACTGCA[C/T]GTCTTTTACAGAAGT | 114088 |
rs762536945 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007153 | CCTCACTGAGGCTAA[C/T]TGGGTTAGCTCATTT | 114088 |
rs762592891 | snp | C/T | 1.6861e-05 | 0.00290348 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094374 | CGGCACGGATCGCAG[C/T]AGAAGACATCGCACT | 114088 |
rs762620247 | in-del | -/AAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007801 | AACACATATTAAACC[-/AAA]AAAAAAAAAAAAAAG | 114088 |
rs762629561 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018833 | GAATAACTGTAACAT[A/T]TTTTTTCTTTCAGAT | 114088 |
rs762640179 | snp | A/C/G | 3.49469e-05 | 0.00418 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094513 | TCTTGGGGAAGCCGC[A/C/G]GAGCCCCCGGTCATC | 114088 |
rs762687964 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056946 | GGCAATATCTTGTAC[C/G]TGTTAATATTCATCT | 114088 |
rs762717966 | snp | A/G | 3.29701e-05 | 0.00406005 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000839 | TGGGACTGGAGAGGA[A/G]GCTAAACAGAAATTA | 114088 |
rs762742245 | snp | C/T | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983118 | CTCTCTGACTTGTAC[C/T]TTTACCCACATTTAG | 114088 |
rs762769479 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038591 | AATATAAAGAATCTG[A/G]CCCACTACAACAATG | 114088 |
rs762796611 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050254 | GGATTGTAGCTTCCA[C/T]GTGTTGTGGGAGGGA | 114088 |
rs762841087 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091126 | ATATTTGACTTATAA[A/G]ACCATTATTATTATT | 114088 |
rs762847571 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011281 | GATGAATGCATGACA[C/T]TCCTTGAACAGTTTT | 114088 |
rs762855952 | snp | C/T | 1.64757e-05 | 0.00287012 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022948 | AGGCTTCAAACTCCA[C/T]ACTGTTCTCCTGTGT | 114088 |
rs762864792 | snp | C/T | 1.68772e-05 | 0.00290488 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010526 | AACAACAGAACAGTC[C/T]AAGATGGCAGAGGGT | 114088 |
rs762909329 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993808 | ATGTTAGCACCACAG[C/T]GGACTGTGCTGAGCA | 114088 |
rs762915680 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022847 | CACCTTCAGCTTGTG[C/T]TCATGCTCCTTGTTG | 114088 |
rs762925959 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034314 | AACCCAATGAGAATT[C/T]AGGCCTTAACTAGGA | 114088 |
rs762925964 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001859 | TAGAACACCCACTGT[C/G]AGCCTGGTGCGTGGA | 114088 |
rs763020290 | snp | A/G | 0.017672 | 0.0923239 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025378 | GCAAAGACAAAGAAG[A/G]AAGCCATGGAGCTGT | 114088 |
rs763037145 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51096023 | CTTTGGTTCGGTTGA[A/G]GCAAGAACAGTTTGT | 114088 |
rs763041893 | snp | A/G | 1.71346e-05 | 0.00292694 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982112 | CAGGCCACTGGGAAC[A/G]ACAGAAGGGAATCAG | 114088 |
rs763062445 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059987 | ACAAATTGTTTCTTA[A/C]AAAAGTGTTTTATCC | 114088 |
rs763076278 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993234 | TGCTCACCTGGGATG[G/T]GAGGGAGCTGGAGGA | 114088 |
rs763094032 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021181 | GACAGTTTTTTAGCA[A/G]TGTTAGGCCAGGTGC | 114088 |
rs763096731 | snp | C/T | 2.34387e-05 | 0.00342327 | intron-variant, synonymous-codon | TRIM9 | GRCh38.p7 | 14:50998001 | GCTTGCCAGCCACTT[C/T]AGATGCCACGCAGTT | 114088 |
rs763111022 | snp | C/T | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982408 | CCTTCACCTGGTGAC[C/T]GGCAGAACAGTGCAC | 114088 |
rs763116695 | snp | A/G | 9.88989e-05 | 0.00703134 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025252 | TTCCTTGCGTCCCAG[A/G]TAACACCCATACCTG | 114088 |
rs763144700 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081591 | TAGACTCCACAGCAG[-/T]TAAAGGATCAGTCCC | 114088 |
rs763170318 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033191 | ACCTCCCGGGTTCAA[C/G]CAATTCTCCTGCCTC | 114088 |
rs763208018 | snp | A/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975845 | CAAGGGTAACCTATG[A/T]AAGTCTATCTCTATA | 114088 |
rs763220267 | snp | A/G | 3.29728e-05 | 0.00406021 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998115 | TTGTTGAAGGCCTTG[A/G]CCCGAGCGTTGTATG | 114088 |
rs763223599 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022191 | TTATAAAAGTATTAA[C/G]AGGTGGAGCCTTTAA | 114088 |
rs763225007 | in-del | -/AT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058783 | CTCACTATCACACTA[-/AT]TCAAAATGACAAATG | 114088 |
rs763254107 | in-del | -/T | | | intron-variant, frameshift-variant | TRIM9 | GRCh38.p7 | 14:50979342 | GGCAGCCTTTGAACC[-/T]GGTAGCCAGCAACAG | 114088 |
rs763256784 | snp | A/G | 1.64857e-05 | 0.00287099 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009108 | GAAATCCAGCTGGTG[A/G]ATGGATTGCAGCAGA | 114088 |
rs763277927 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095161 | GACCGCCCCTACCTG[C/T]CCTCCTAGTCCCGCC | 114088 |
rs763295787 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985787 | CCACACAAACAAGAA[A/C]GCCACAAAGCTCCAC | 114088 |
rs763310865 | snp | A/G | 1.65927e-05 | 0.00288029 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979547 | GTGATCCCTCCCTCA[A/G]TTCTGTAGGAAAAGA | 114088 |
rs763336490 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093630 | TCCCCGACCCTCCGC[C/T]GTGCCTCACCAGGTC | 114088 |
rs763419972 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043616 | ATTTGGATGGGAAAC[C/T]AAATATTAGGATTCA | 114088 |
rs763459840 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004571 | AACAGGGAACACTAA[C/T]CATAAGGGATGCTTT | 114088 |
rs763466451 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029237 | ATCTGAAGTTACAGG[C/G]ACAGGATGGGTCAAA | 114088 |
rs763476255 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998877 | GCAAAATTATGCTGA[A/T]GTAATGAATAAAAAT | 114088 |
rs763497912 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016330 | CTTTCAGATCAGCAG[C/T]GGCATTAGATTCTCA | 114088 |
rs763546625 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022037 | CAAAATTTCCACCCC[-/T]ATCCCCAGTACTCAC | 114088 |
rs763581860 | snp | A/C | 1.67323e-05 | 0.00289239 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010510 | CTAGGATTAAAAAAA[A/C]AACAACAGAACAGTC | 114088 |
rs763600941 | in-del | -/TTTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027133 | ATGCTGGCTGTTAAC[-/TTTTTTTTTT]TTTTTTTTTTTTTTT | 114088 |
rs763604743 | snp | C/T | 1.66679e-05 | 0.00288681 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010339 | ATCCTAGACTATGTC[C/T]TATGGGACATTTAGA | 114088 |
rs763608897 | in-del | -/TTTTTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077387 | TCATCTCCAATTCTG[-/TTTTTTTTTTTT]TTTTTTTTTTTTGAG | 114088 |
rs763621508 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037511 | GATCAGATCAGAAAA[A/G]AAAGAGGGGGCTTTT | 114088 |
rs763694124 | in-del | -/CAAAAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068328 | GTATTTGGTGTGCAC[-/CAAAAA]CAAAAACAAAAACAA | 114088 |
rs763750234 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976180 | GCAAATAAGAATGCT[G/T]ACATCATTTCTACCA | 114088 |
rs763806690 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058753 | GCCCCTTCAATTCAG[C/G]TACATATGGTGTGAC | 114088 |
rs763837718 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980389 | TGAGATCTAGCAATA[C/T]TGAACTTCGTCCTCA | 114088 |
rs763881872 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092822 | AACATAATTAAAATA[C/T]ATAGCATGCCACACA | 114088 |
rs763903391 | snp | C/T | 1.64806e-05 | 0.00287054 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009164 | AGTCCGTGGTCATCC[C/T]TGGAGTGAGTGTGCC | 114088 |
rs763910794 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019983 | TGCGTAAGTACACAC[C/T]CACTTTCCAGCATTC | 114088 |
rs763928677 | in-del | -/CTC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001337 | CGGGTTCACACCATT[-/CTC]CTGCCTCAGCCTCCG | 114088 |
rs763929803 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000413 | GCATTGTCCACATAG[C/G]TAGGGTGGAGGAGAC | 114088 |
rs763961153 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998934 | TATGACAACTCTCTG[G/T]TAGGATACTAAGAAG | 114088 |
rs763986949 | snp | G/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979209 | AGAAGGTGCTTATGC[G/T]TGGCGTGGAATAAAA | 114088 |
rs764002735 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030557 | AGTATAGGGACAAAG[A/G]ATGTGTGTGTGTGTA | 114088 |
rs764002913 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019123 | TGTGAGGAGCACAGA[C/T]AGGAAATGTAGGCTT | 114088 |
rs764037350 | snp | A/C | 1.84971e-05 | 0.00304109 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094588 | TGCGGGGCACCGGGG[A/C]CAGGGCCGGTGACAA | 114088 |
rs764081038 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040423 | CCGACATCTAGTCCC[A/G]TGGTAACTGCCTACT | 114088 |
rs764088810 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075099 | TAACTGGGACCTTAG[C/T]TCTCATGTAATCCTG | 114088 |
rs764098743 | in-del | -/TGT | 1.64751e-05 | 0.00287007 | cds-indel, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000778 | AGGACAACGTAGCGC[-/TGT]TGTTGTGGGTACAAC | 114088 |
rs764113347 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002419 | GATTAGAGATATGAG[C/T]CACCGTGCCCGGCTG | 114088 |
rs764179816 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070693 | CAACCTGCACTGGGA[A/G]TAACAGGGATTGACT | 114088 |
rs764189506 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014367 | CATTCTATGACTCAA[G/T]CTCCTTGGAAGGACT | 114088 |
rs764242167 | snp | G/T | 9.96082e-05 | 0.0070565 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979347 | GCCTTTGAACCGGTA[G/T]CCAGCAACAGCTGTT | 114088 |
rs764244847 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091501 | GCATAGAAATTCTGG[A/C]CCATGGGCTTTTGTG | 114088 |
rs764290456 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991581 | TTCCTTATATGATCC[C/T]TTATCAATCATTTTC | 114088 |
rs764304338 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | TRIM9 | GRCh38.p7 | 14:51094076 | GCAAAACCGGATGAT[C/T]GGAGACGCAGGGAGT | 114088 |
rs764308922 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003243 | ACGGAAGATAAATAT[A/G]ACAAGTTTTGGGAAA | 114088 |
rs764309582 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093513 | TGGCTGCCCTCTCCG[C/T]TCTGTCTTTTGAGCA | 114088 |
rs764320710 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047696 | CGCATATAACAATCT[C/G]TATCAGGTAAAAAAG | 114088 |
rs764332094 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979427 | GCAGGGAAGAAGAGG[C/T]CCTCCACGTTATCAA | 114088 |
rs764332512 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057964 | ATTTCAAGCCAGTTT[A/C]CTCTGATTTTAAATT | 114088 |
rs764342412 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022866 | TGCTCCTTGTTGACG[C/T]GGGCCAGCAGCTGGG | 114088 |
rs764383678 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990345 | TATTTGTTCATTAGC[C/T]AACGCTATTGAACAC | 114088 |
rs764414955 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062241 | TTAATATGCTTACTA[C/T]ATTTATTTTGAAATG | 114088 |
rs764461230 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022629 | TGGCTGAGAAAAGTC[A/G]CCCAACAAACATTAT | 114088 |
rs764467129 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995442 | AGCACTGCCCAATAA[A/G]TAGACAGATAAATTT | 114088 |
rs764526523 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049135 | AGCGCAGTCCCGGCT[C/T]ACTGCAGCCTCTGTC | 114088 |
rs764555643 | in-del | -/AAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987012 | CTTTCTATTTTGTCA[-/AAC]AACAATAGCTGGTTC | 114088 |
rs764572091 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023485 | AAGGAAAGCAAATAG[C/T]AGGCAGAAAAAAACA | 114088 |
rs764583928 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094205 | GTAGCACACGGGCAT[C/T]TTGCATTGCACGCAG | 114088 |
rs764608782 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988468 | ATGGTTATGGCTCTT[C/T]CTATCCTTCCATGTG | 114088 |
rs764658590 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086307 | TTCCTGTGTTCCAGT[C/T]TTCTCACAGGAAGAT | 114088 |
rs764681313 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984153 | GCCTAGTCTTAAAAT[A/G]TTCAAAAGTGTGTGA | 114088 |
rs764681363 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006217 | ACAATTAGAAAATAC[A/G]TATTGGATTACATGT | 114088 |
rs764690932 | in-del | -/TAGGG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080044 | TTTTGTGCTTTTTGC[-/TAGGG]TAGGAGTCAACCAGA | 114088 |
rs764726580 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091603 | TTAAGTAAATAAGGT[C/G]GGGGAGTAATGTTTG | 114088 |
rs764731579 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067678 | CCCTTCCTGCAGATC[-/T]TCACAGAGGGCTGCC | 114088 |
rs764747927 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027314 | ACACCGAGTGAACTT[C/T]TGTATTTTTAGTAGA | 114088 |
rs764756569 | snp | A/G | 0.000115316 | 0.00759243 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981982 | GTAGTGGATGCCCTT[A/G]GAGAAGCCAGTCTTC | 114088 |
rs764778138 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994149 | GGTGGCTCATGCCTG[G/T]CATCCCAGTACTTTG | 114088 |
rs764789100 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065571 | GAAGTAAGGACACAC[A/G]TTTTTGCCCTCCTTT | 114088 |
rs764790408 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017975 | TATGCCAAATGAAAC[C/T]CTGAAAGGAATTCAT | 114088 |
rs764798049 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033928 | TATAGAAGAGAATAT[A/G]CCCATTGAATGTTTA | 114088 |
rs764819055 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084245 | GGTGTAAATATGCCA[A/T]TTTTGAACCATTGTT | 114088 |
rs764833081 | snp | A/G | 1.64923e-05 | 0.00287156 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094231 | CGCAGTACATGCTGT[A/G]GTTCTCCAGCTCGTG | 114088 |
rs764835029 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978448 | AGAGTCTCTCCACCA[C/T]TCCTTGCCCATGCAA | 114088 |
rs764843438 | snp | A/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996208 | ACACAATATATAAAA[A/T]TCATGGAGGAAATTA | 114088 |
rs764933993 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994229 | TGGGCAACACAGCAA[A/G]ACCACATCTCTACAA | 114088 |
rs764986316 | snp | C/T | 3.80575e-05 | 0.00436203 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977391 | CTGAGAGGCATCGTG[C/T]ATCCCCCTGTCCCTT | 114088 |
rs765007336 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076891 | TAGCAGTAGACCCTG[A/G]AACAGATTCTAGTTT | 114088 |
rs765028909 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045148 | TGCAAGCCACCAGCT[C/G]CTCAGCTGGTGAGCT | 114088 |
rs765041137 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001219 | AACGTGCCTGAAGCT[-/G]TGCTAATAATTTTTT | 114088 |
rs765057735 | snp | C/T | 1.94441e-05 | 0.00311796 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094787 | CCCGGAGCCCGCGGC[C/T]CGATGGCTCTGGGGG | 114088 |
rs765079878 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998295 | CCTGGTGTCATTCTA[A/T]TCTGGATTTGAATCC | 114088 |
rs765182315 | snp | C/G | 4.98087e-05 | 0.00499017 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010357 | TGGGACATTTAGAAT[C/G]TGACGCAGAAACTAG | 114088 |
rs765235487 | snp | A/C | 1.67964e-05 | 0.00289792 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010517 | TAAAAAAAAAACAAC[A/C]GAACAGTCCAAGATG | 114088 |
rs765238374 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042848 | CTTATTCCAGATCCA[C/T]TCTCAACCTTCTCTG | 114088 |
rs765241562 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999889 | ATGCCGGCAGGTGGT[A/G]GCACATGAATCATCA | 114088 |
rs765248056 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991784 | AGCTGTAAGTCCATG[A/G]TTTTAGAGATGAGAA | 114088 |
rs765264210 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003374 | TATGCTCTTATTTCA[-/T]TAGCTCCATATTAGT | 114088 |
rs765331898 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042478 | ATTTCCCTTTTAAAT[C/T]TTTTATTTCTAGTTG | 114088 |
rs765368382 | snp | C/T | 1.65351e-05 | 0.00287528 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979537 | GGCCCCTTTTGTGAT[C/T]CCTCCCTCAGTTCTG | 114088 |
rs765380593 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071267 | TGTAATCCCAGCTAC[C/T]CTGGAGGCTGAGGCA | 114088 |
rs765417560 | snp | C/T | 0.0002252 | 0.0106089 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985957 | GGAGCTCAGCTCACC[C/T]GGTGCATTGAGAGAC | 114088 |
rs765419217 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032112 | TAAATAATAATTTAA[A/G]TCTAAACATGCTGTT | 114088 |
rs765448643 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980581 | GTTCAGCATTAAGAA[C/T]GTGTTTCTCTGCATA | 114088 |
rs765465611 | snp | A/G | 9.89593e-05 | 0.00703348 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000741 | CCATCGGCGGGCACC[A/G]TGGACAGAGGTGGCT | 114088 |
rs765471142 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070753 | AAGATAGACTGAGGG[C/T]CACATATTATTAGAA | 114088 |
rs765507859 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059951 | CAGGTTGCAAATAAC[A/G]CATTAAATGGAAAAT | 114088 |
rs765530241 | snp | A/G | 1.65061e-05 | 0.00287277 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009225 | TCTTCTTATGAGGGC[A/G]TCAGAAATCTAATCA | 114088 |
rs765559827 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020143 | CTGCAGGACAGTGAG[C/T]GATGGGTTAGCCAAC | 114088 |
rs765582524 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013348 | TGAGCAAGTATGTAA[A/G]AGTTTATTTCTGGAT | 114088 |
rs765583636 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051494 | AGGCAGTCTTACCTC[A/G]TAGGCCTTTGCTACA | 114088 |
rs765596401 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984469 | AAAGAATCGTTTCCT[C/T]CCATCTCATGGCTGA | 114088 |
rs765648182 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063529 | TCAAAAAACAGCAGA[A/G]GTACACATACATATG | 114088 |
rs765698788 | snp | C/G | 1.65042e-05 | 0.0028726 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979360 | TAGCCAGCAACAGCT[C/G]TTTAACCTCAGGGGC | 114088 |
rs765701217 | snp | A/C | 1.64803e-05 | 0.00287052 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000828 | ATAGGGGTTGCTGGG[A/C]CTGGAGAGGAAGCTA | 114088 |
rs765701276 | in-del | -/A | 1.68454e-05 | 0.00290214 | intron-variant, frameshift-variant | TRIM9 | GRCh38.p7 | 14:50979337 | CCCTGGGCAGCCTTT[-/A]GAACCGGTAGCCAGC | 114088 |
rs765729690 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036204 | GGCACAAAAAAGCCA[A/G]CATCTCTTCCATATT | 114088 |
rs765731352 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023610 | GCTTCCCTGTGATGT[G/T]TAAATTAAATGCTGG | 114088 |
rs765746533 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060676 | GTTTCGCCGTGTTAG[C/T]CAGGATGGTCTCGAT | 114088 |
rs765762676 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010887 | TGCTGCTGCAGCTGT[G/T]CTTGGTGACACTGTC | 114088 |
rs765780133 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041322 | TGATAAGCTTGCACA[G/T]GCAAGGGCGGGTTAC | 114088 |
rs765831736 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975787 | TTAGAACTTCTTTCC[A/G]GGTCCTACCTTTCCT | 114088 |
rs765899325 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018285 | CCTGCCTGCCTGCCT[G/T]CCTTCCTTCCTTCCT | 114088 |
rs765911788 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062377 | CTCACAACTTTTTAT[C/T]GTATACCAGAAACTG | 114088 |
rs765933911 | snp | C/T | 1.68179e-05 | 0.00289977 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094393 | AGACATCGCACTGTT[C/T]GCACATGACGGTGGC | 114088 |
rs765967967 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086693 | GAATACAGATATGGA[C/T]GCTATGGAGGAGGGT | 114088 |
rs766001774 | in-del | -/TC | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977448 | TAACTCAAAAAGTGT[-/TC]TGTTTGCTTCGCTTT | 114088 |
rs766011399 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995463 | AGATAAATTTGCTTT[C/T]GAAGAAAAAACCAAT | 114088 |
rs766019258 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075019 | CATTTTTATCCAAAG[A/T]GACTCTTGTCAGGAA | 114088 |
rs766028649 | snp | C/G/T | 0.000164715 | 0.0090736 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979411 | CCTGTTCAGGCTGAC[C/G/T]GCAGGGAAGAAGAGG | 114088 |
rs766031274 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996703 | ATTTTGAGAAAAGAG[A/G]CAACTGCTCTCAAAC | 114088 |
rs766075809 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027434 | CAGGTGTGAGCCACC[A/G]TGCCCAACCAGCTGT | 114088 |
rs766132190 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067536 | ATTAGACCCCCATCT[A/G]TCTCTCTGACCTTAT | 114088 |
rs766201436 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034607 | TTTCACCTCGGGAAA[C/T]AGGAATAATCAAGAA | 114088 |
rs766222499 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079691 | CTTCACTGGGAATGA[C/T]GCCAGGGCTGGGCAA | 114088 |
rs766306759 | in-del | -/C | 3.29641e-05 | 0.00405968 | intron-variant, frameshift-variant | TRIM9 | GRCh38.p7 | 14:50979375 | GTTTAACCTCAGGGG[-/C]AGGGTGCTTACCTGC | 114088 |
rs766344041 | snp | C/G/T | 6.59049e-05 | 0.00574012 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982019 | ACCACCCGGTCATCA[C/G/T]AGCTACTACAGGTCA | 114088 |
rs766347048 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016975 | CAGGAGGGAGTTTCT[A/G]TGTGTCCCATTGTGT | 114088 |
rs766376239 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024549 | ATGCTAAACAGTACA[C/G]AAGGTCATTATTTTA | 114088 |
rs766379620 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028408 | TTTTTATAGGTTGGT[A/G]TTTTAATCACATTTA | 114088 |
rs766424417 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021237 | CTCAGGCCTAACCAG[A/T]TGGAACAAGACCACA | 114088 |
rs766435792 | snp | C/T | 8.82029e-05 | 0.00664031 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50998007 | CAGCCACTTTAGATG[C/T]CACGCAGTTCTCGCT | 114088 |
rs766442889 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993824 | GGACTGTGCTGAGCA[C/T]TGGCGGCTTAAAGTC | 114088 |
rs766447939 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091226 | CTGGCCAGTTGAAAA[C/G]TAGTGAATTTCAACC | 114088 |
rs766462919 | in-del | -/ACACACACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080437 | ATTGAGTTTTATTGA[-/ACACACACAC]ACACACACACACACA | 114088 |
rs766525625 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078591 | GAGGAAATTATGCTA[C/T]GTGAAGTAAGCCAGA | 114088 |
rs766538028 | snp | C/T | 1.76428e-05 | 0.00297003 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977300 | ACATCCTTAGGCTAT[C/T]GATGCTCTGCTGGAG | 114088 |
rs766579413 | in-del | -/GCCT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018272 | GAGCTGGGATGGCCT[-/GCCT]GCCTGCCTGCCTGCC | 114088 |
rs766582122 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060048 | CCAAAAGTAGATTCC[A/G]CCAAACTGGGAGTCA | 114088 |
rs766603858 | snp | A/C | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979448 | ACGTTATCAAATGCT[A/C]TGGGACCTTGTTGTT | 114088 |
rs766631987 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980965 | TTTCCCTTTGATCTG[A/G]TTGAACACTACTGTA | 114088 |
rs766646794 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054607 | TTTTTTTTAGAAGGA[A/G]TTTCGCTCTGTCGCC | 114088 |
rs766671210 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989591 | AGCTCCTGAAGAGAC[A/G]TTTAACATCACATCA | 114088 |
rs766692137 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010937 | TTTACTTGTAAAGAG[C/G]AGACATCACCATCTG | 114088 |
rs766706669 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003546 | TGTAGACATAGGTAT[A/C]ATTAAAAAAGTAACT | 114088 |
rs766766701 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095175 | GCCCTCCTAGTCCCG[C/T]CCCGGCCCATGAGCA | 114088 |
rs766773406 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992779 | GGGCAGCGTGATGCT[C/G]AGAGTCTAATCGGGG | 114088 |
rs766810800 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975885 | GATGCATTATTATTC[G/T]GCTATCAGTCATAGT | 114088 |
rs766821552 | snp | C/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977027 | AAAATCTGGGAGTGG[C/G]AACCAAGTGACTTGG | 114088 |
rs766835464 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082232 | ACCACGGACAAAGAC[C/T]AAATATATTTTTTAC | 114088 |
rs766896966 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008587 | AATTTTAAAGTTTAT[A/G]TCAAATTTCCATTTT | 114088 |
rs766906505 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062697 | AGCTGGAAATTGAGA[C/G]GGGAATCCTTGAAAT | 114088 |
rs766913285 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063644 | TAAGTAACAGCTGAC[C/T]TCTCACCAAAAACAA | 114088 |
rs766920291 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030863 | TTATAAGAAAGATTC[A/G]AGGCCGGGCGTGGTG | 114088 |
rs766941627 | snp | G/T | 1.64993e-05 | 0.00287218 | intron-variant | TRIM9 | GRCh38.p7 | 14:51023005 | CTGCTGGGTGCCTCA[G/T]GCTGCCAGAGAAAAC | 114088 |
rs766961444 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043023 | TTAATAGCATAACTT[A/G]CTTATAAGAGGTCCT | 114088 |
rs766994666 | snp | A/G | 1.7703e-05 | 0.0029751 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094535 | CCGGTCATCCAGGAT[A/G]AGGCTGCGGTGACAC | 114088 |
rs767016200 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047358 | GGCCACGGCATTCAT[C/T]TCATCATGGCTGTTT | 114088 |
rs767048850 | in-del | -/AAA | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974999 | AGTGAGATTCCGTCT[-/AAA]AAAAAAAAAAAAAAA | 114088 |
rs767051464 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004642 | TACAGGTATTCACTC[A/C]TTTAATTTTCACAAT | 114088 |
rs767059962 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035380 | CTATCCTTTCTTAGC[A/T]CTAATATTTGAGTCT | 114088 |
rs767077541 | snp | C/T | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009153 | ACTCAAGTCAAAGTC[C/T]GTGGTCATCCTTGGA | 114088 |
rs767110836 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076554 | GTTTATTACAAAAGG[A/C]TTTCTCATACATTCA | 114088 |
rs767115993 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024888 | ACTGTGGCCTGTTAC[C/G]ATTAAATGATACAAT | 114088 |
rs767157850 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976819 | CATTCTAGCAGGTAA[A/G]CTGTATGCTACAAAT | 114088 |
rs767160869 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018473 | ATGCCAATAATATCC[A/G]TAACGTAAATTTGTG | 114088 |
rs767163287 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50984659 | CATGCCTTGTGCAAC[A/T]CTTTTTCAAAACAAA | 114088 |
rs767198779 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088498 | AAACAAAAAGAATTG[C/T]GGAGTGCTCATACAT | 114088 |
rs767233744 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082619 | AGTTGTGGGGTTTTA[C/G]TGGTGACTTAATAGT | 114088 |
rs767247298 | snp | C/T | 1.64857e-05 | 0.00287099 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022979 | AACAGAGCACATTTC[C/T]CAACTGCAAGCTGCT | 114088 |
rs767273199 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069029 | GGGTGCCAGTTAGGA[G/T]ATTATTTCAATAGTG | 114088 |
rs767291040 | snp | A/G | 1.75228e-05 | 0.00295991 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982128 | ACAGAAGGGAATCAG[A/G]TTATTAAGACAGACC | 114088 |
rs767301487 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053557 | TACATTTATTTATTT[-/A]TTTTTTTTTACTTTT | 114088 |
rs767366071 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029139 | GTAAACATTCTTCAC[A/G]TGGCCTTTTCCCCTC | 114088 |
rs767390151 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058694 | CAGAACAGATATACT[A/C]AGCTGTCTTTTACGT | 114088 |
rs767444994 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998171 | AGTGCACATTGTCTC[C/T]TTCCCCACATACACC | 114088 |
rs767455948 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040931 | AGAAACTCTCTGAGA[C/G]ATCTCAAATAGCTTC | 114088 |
rs767500958 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086955 | TGAATCAGCCAAAAT[A/G]AAGAAAACTCCCTCT | 114088 |
rs767518826 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011465 | CAAGTAGCTGGGACT[A/G]CACTGCAGCTATCTT | 114088 |
rs767533110 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051178 | CCAGTTACAAAAAAA[-/T]ATTATCATACCCAGA | 114088 |
rs767558425 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980348 | CCATTAAAAATGGAC[A/G]ATCAGATTTGTCTTT | 114088 |
rs767559006 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019040 | GAAAGTGGCATATGT[A/T]AAGTTTCTGAAGAAA | 114088 |
rs767561635 | snp | C/G/T | 5.84326e-05 | 0.00540495 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977402 | CGTGCATCCCCCTGT[C/G/T]CCTTTACACAGTGTA | 114088 |
rs767604777 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022553 | CCCTCTTGATAGAAT[A/G]TAAGTCCCATGAAGG | 114088 |
rs767636523 | snp | C/T | 1.65007e-05 | 0.00287229 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000730 | CCAGAATGTATCCAT[C/T]GGCGGGCACCGTGGA | 114088 |
rs767641703 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079790 | GTGGTCAACGACCTA[C/G]AGCTAGATGAAAAGA | 114088 |
rs767712529 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065223 | CTTCAATATGTGTGA[A/G]ATGTTCCAGGAAAAT | 114088 |
rs767724265 | snp | A/G | 1.68103e-05 | 0.00289911 | intron-variant, stop-gained | TRIM9 | GRCh38.p7 | 14:50979338 | CCCTGGGCAGCCTTT[A/G]AACCGGTAGCCAGCA | 114088 |
rs767759261 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988874 | CAGGAGTCTTAGAGG[A/G]AAGAAACTTAATATC | 114088 |
rs767825690 | snp | A/G | 6.58903e-05 | 0.00573941 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981837 | GCATGAACCAGCTCC[A/G]GTTATTGTCCACATA | 114088 |
rs767828227 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987287 | ATCAAAATGTTACTC[A/G]CATGTTGAAGCAAAA | 114088 |
rs767842292 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073337 | CATTTATGCACCAAA[A/G]GACAGGTGCTATAAT | 114088 |
rs767847693 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000194 | ATAAATCTTGGACAA[C/T]GGTTAATTATATTAT | 114088 |
rs767860490 | snp | A/C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090447 | ATATTGTTTAAATTG[A/C/T]AAATTTTCATTTATA | 114088 |
rs767871571 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091953 | AGATTTAAAGGTTTC[C/T]TTTGGTCTTAATAGA | 114088 |
rs767889544 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993903 | CATAAGTAGAGAAAG[A/G]TGACAATAATAATAC | 114088 |
rs767901331 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982591 | CTTTGAAGTCTTCCT[C/T]GGCTCTAGTGAAAGC | 114088 |
rs767913210 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032420 | AGATTACCCTAGGAA[C/T]TGCTCTTGGCCACAG | 114088 |
rs767934219 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084071 | TAGTATTTAAAAATA[C/T]ATGGGAAATATTTAT | 114088 |
rs767951329 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005383 | CAATGGTCTATGTGC[C/T]AAAAAGGCTTGGTGA | 114088 |
rs767953814 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018256 | ATTTTTAATTTTTTT[-/G]TGAGCTGGGATGGCC | 114088 |
rs767971210 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074088 | CAATCACTGAATAAT[A/T]GTAATGATCATAACA | 114088 |
rs768051281 | snp | C/T | 4.94279e-05 | 0.00497107 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025326 | GCTTCTTTGGCCCTG[C/T]CTGACAGTCCGTTCA | 114088 |
rs768054941 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021320 | CAGGTAGGAATGTAA[A/G]TGGTCATTAACACAC | 114088 |
rs768099748 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050041 | TAAACGATGCAGAGC[C/T]GTGAGACAGTTTTTA | 114088 |
rs768127222 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995252 | AATTTTATCTTCCTG[C/T]TAATCCCTTTTCCCT | 114088 |
rs768143599 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993902 | CCATAAGTAGAGAAA[C/G]ATGACAATAATAATA | 114088 |
rs768171113 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028010 | CCAACCTTGCAATTA[A/G]TTGTGTCTGTATAAG | 114088 |
rs768223359 | snp | A/C | 2.16106e-05 | 0.00328707 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094887 | AGGATGATGGGCTCC[A/C]GATAGAAGGAGCCGC | 114088 |
rs768235426 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077338 | TGAGGTAAGGCGACC[A/G]TGAGCTGTCAAACTT | 114088 |
rs768244337 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060737 | CTCCCAAAGTGCTGG[G/T]ATTGCAGGCGTGAGC | 114088 |
rs768262294 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982890 | ACCTGTGAGACACCT[C/T]ACATGCACTTTGGTC | 114088 |
rs768290408 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079034 | ACAATTTATTTTAAA[A/G]TAAAATAAAATAAAA | 114088 |
rs768290500 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51056258 | GCAATTCTTTATCCT[G/T]CAAGAGAATGAAAAA | 114088 |
rs768333794 | snp | C/T | 3.29891e-05 | 0.00406122 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022813 | TGTTGGCTTTCTGCT[C/T]TTCCCATGATGCAGC | 114088 |
rs768391916 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095371 | GGGACCGGGAAGGAG[G/T]AGTTAGGCGGGATGA | 114088 |
rs768392157 | snp | A/G | 1.65244e-05 | 0.00287436 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025371 | TGGCTCTGCAAAGAC[A/G]AAGAAGGAAGCCATG | 114088 |
rs768394379 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005118 | CTGTTAAAGATAACC[C/G]TGAACGCAGGTTTTG | 114088 |
rs768410245 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089947 | TACCTTATCAAAATC[C/G]TTTCACAATTGTAAT | 114088 |
rs768413135 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057898 | ACACAAGTTTATCCA[C/T]TAAAGATCAGTTAAA | 114088 |
rs768419707 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985819 | ATCCCGATGCTCCTC[A/G]TACGGAAAGCAGGCC | 114088 |
rs768442936 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010275 | TGAGGTAGGTTCTGT[A/T]ATTGAGGGACACAGG | 114088 |
rs768445636 | snp | A/C/G | 3.31825e-05 | 0.00407313 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998085 | AGGGTCTTGCTGTAC[A/C/G]GGCTGACTCCTGTTT | 114088 |
rs768449747 | snp | C/T | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979515 | AGTCGAGGAGGACCC[C/T]AATTGTGGCCCCTTT | 114088 |
rs768455691 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044067 | AATTAAATTTTTAAA[A/C]AATTTTTAATTTGTT | 114088 |
rs768511695 | snp | A/C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071186 | GTTCAAAACCAGCCC[A/C/G]GACAACATGGCAAAA | 114088 |
rs768528776 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060434 | CTCCACATAATGTAT[G/T]TGAGACTCATTCTTA | 114088 |
rs768532765 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032873 | CTGAAAATCCAAAAT[C/G]TGAAACATTTCAATG | 114088 |
rs768553368 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025814 | GGGGTAGGTACTGGT[A/G]TGATCCTCTGGGGCC | 114088 |
rs768579292 | snp | A/C/G | 5.65353e-05 | 0.00531648 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977388 | GTCCTGAGAGGCATC[A/C/G]TGCATCCCCCTGTCC | 114088 |
rs768608113 | snp | C/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097078 | ATCTAAGAGATCTTA[C/T]TAGCAGAAAGTTTAT | 114088 |
rs768608338 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052480 | TATTTTTGGCTGTTG[C/T]TGCTATTAGCGTCAT | 114088 |
rs768627874 | in-del | -/TAGAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025774 | GTAGGGCAGAAAGAA[-/TAGAG]TAAAGAACAGGATGA | 114088 |
rs768821163 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51015038 | GCTTTTAAAATTTTA[C/T]CAGCGGAGCCACCAT | 114088 |
rs768843760 | snp | C/T | | | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094441 | CGCAGAGCTGGCACT[C/T]GAGGGCCGCGGCTTT | 114088 |
rs768863786 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022904 | TCTGTTGAGGGCATC[A/G]ATGAGGGCATCACAT | 114088 |
rs768866032 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007098 | AAAGCATTTCAAAAC[C/G]CTGAGGCTTTTACCC | 114088 |
rs768880711 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037079 | CATGTAAACCAAGAT[C/T]TGTCCATGATTAAGT | 114088 |
rs768893093 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985407 | CTTTTGCAGAAAATG[A/C]TTTCACTTTCTGCTC | 114088 |
rs768928043 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976777 | CTCTGCAGAGCTAAC[A/G]CTACAGGAGAGGTAA | 114088 |
rs768931756 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095731 | GCGCTGGCGCAAGCC[C/T]TGGCGACACTCTTGG | 114088 |
rs768960517 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082952 | GTCTTGGCACTTGTG[A/G]ACTGTGACTTTGGGT | 114088 |
rs768973063 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019542 | CACTAAAGAATCTCC[C/T]AGGTTCATGGATAAT | 114088 |
rs768977601 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074896 | GATGCCGCAACTACA[C/T]GGTTCATCTCCTTTT | 114088 |
rs769014959 | snp | A/G | 1.6477e-05 | 0.00287024 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094354 | GGGGCGGGTGGCAGC[A/G]CAGGCGGCACGGATC | 114088 |
rs769021751 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50975325 | TTTTCTAGTATAGTA[C/G]TTGTATGCATCTGTA | 114088 |
rs769026924 | snp | C/T | 1.66632e-05 | 0.0028864 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982086 | GCGCCGAGCCAGGGT[C/T]GAAAGCAAACCAGGC | 114088 |
rs769031009 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986604 | ACTGTTTCCTATTCC[A/G]TATTTTCCCATTTCT | 114088 |
rs769042218 | snp | C/T | 1.65633e-05 | 0.00287774 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981776 | CCAACGTGAAGAAGG[C/T]TTGGTTTGGGGGCTG | 114088 |
rs769082606 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028821 | CTGAGAATCACCGAG[G/T]TCTCCCAGAAAGATG | 114088 |
rs769083221 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047131 | TGAGCTGGGGTTGAC[A/G]CTTGTGTTTACCATG | 114088 |
rs769085404 | in-del | -/CAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006014 | TTTCTTTTTTATCAA[-/CAA]CAACAACAACAAAAA | 114088 |
rs769157919 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076137 | AGGAGGTGGTGTGTT[C/G]CCTGTTTCACAGATG | 114088 |
rs769179957 | in-del | -/CT | 5.78235e-05 | 0.00537665 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977398 | GCATCGTGCATCCCC[-/CT]GTCCCTTTACACAGT | 114088 |
rs769182106 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024544 | TAAGAATGCTAAACA[G/T]TACAGAAGGTCATTA | 114088 |
rs769209311 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039987 | ACGGGGTTTCACCGT[A/G]TTAGCCAGGATGGTC | 114088 |
rs769222939 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008382 | CTATTTTTGTAACTT[A/C]TTGTGTATTTCAAAA | 114088 |
rs769245905 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051838 | CAGGCATGGTGGCAT[A/G]TGCCTGTGATCCCAG | 114088 |
rs769310667 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080914 | TTTCCTGTTTGTCAA[A/G]GCCAATCTAGATGGA | 114088 |
rs769324025 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990971 | GGTACATAATTTATA[A/G]TAAAAGGTGGTATTT | 114088 |
rs769351157 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035935 | GACAGAGCCTTGTAC[A/C]GAGTAGTAGTGACTT | 114088 |
rs769381480 | snp | A/C | 1.64798e-05 | 0.00287047 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022828 | CTTCCCATGATGCAG[A/C]ACTCACCTTCAGCTT | 114088 |
rs769406380 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51090717 | TTCTCCTGCCTCAGC[C/T]ACCCAAGTAGCTGGA | 114088 |
rs769411887 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034254 | TTAACACACACTTAG[A/G]TAGCACTCTATGTGC | 114088 |
rs769418095 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097491 | CTGGGATTGGAACCC[A/G]GACACATATAAGTTT | 114088 |
rs769430780 | snp | C/T | 1.64738e-05 | 0.00286995 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022925 | GGCATCACATTGGGC[C/T]ACCAGACAGGCTTCA | 114088 |
rs769440984 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51036214 | AGCCAACATCTCTTC[A/C]ATATTAGCAACGTCA | 114088 |
rs769478790 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979276 | CCTTCATATCTTGGT[C/T]TGGGCCTTACGCTGT | 114088 |
rs769491322 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025811 | GAAGGGGTAGGTACT[C/G]GTGTGATCCTCTGGG | 114088 |
rs769499206 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989631 | ACACGCAGGGATCCC[A/G]TGTGGTTGCAGAGCT | 114088 |
rs769504722 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028865 | GCCTGAAGGAGAGAA[A/G]CAAAGAACTCTGCCT | 114088 |
rs769591113 | snp | C/T | 1.67621e-05 | 0.00289495 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094304 | CACACGACCCTGGGC[C/T]GGGGGCACCAGGCGG | 114088 |
rs769608925 | snp | A/G | 0.000134021 | 0.00818491 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986086 | AGGACTCATTCTACG[A/G]AGCGGCAATCTTTCC | 114088 |
rs769616120 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982254 | GGCAGACAGGGGCAC[A/G]TCCTGGGAGTTGGTA | 114088 |
rs769616222 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994845 | CCTTATTTGAAAATT[G/T]CATTAAAATTCTTAA | 114088 |
rs769636455 | snp | A/G | 1.72653e-05 | 0.00293809 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979329 | ATTGAACGGCCCTGG[A/G]CAGCCTTTGAACCGG | 114088 |
rs769654885 | snp | C/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979398 | TTACCTGCACGTTCC[C/T]GTTCAGGCTGACCGC | 114088 |
rs769677988 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023073 | CTCTGTCCACAATGC[A/C]CATTTGGTAATTTTA | 114088 |
rs769716224 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060528 | CTGGAGTGCAGTGGC[A/G]CGATCTCGGCTGACT | 114088 |
rs769723208 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016306 | CAGGAGGTGAGCGGC[A/G]GCCACCTCCTTTCAG | 114088 |
rs769743481 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025464 | CTCCTCAGATTCCTC[C/T]TGTCTGAGGTTGGAC | 114088 |
rs769767958 | in-del | -/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026926 | GCTTCTGCTAGTTAA[-/G]GGAACAATTCTGAAT | 114088 |
rs769772963 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007033 | GTGAGCAGATGGACA[A/T]GACTCAGGAGGGCAA | 114088 |
rs769811086 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095906 | ATAGCTCGGCCCAGA[A/G]GCCTCAGTGCCGTGG | 114088 |
rs769815405 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988151 | AAATGTATTTTTCAC[C/T]AGGTGTGACAGTCAA | 114088 |
rs769824618 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012314 | AGAACCTCTTACATA[A/T]GTGCAATCATATAAT | 114088 |
rs769848772 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055249 | TAAGAAATAAAAGCA[C/T]GGCCAATTGAAACAT | 114088 |
rs769903140 | snp | A/G | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981932 | CCAAAGGCAGGATCA[A/G]GGTGGTTGTCATAGC | 114088 |
rs769923624 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005135 | GAACGCAGGTTTTGA[G/T]TCCATGCATTTCAGG | 114088 |
rs770000491 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064440 | TAAAGACTAGCAGAC[A/G]GAATAAATAAGTCCC | 114088 |
rs770008376 | snp | G/T | 1.64925e-05 | 0.00287158 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981797 | TTGGGGGCTGCAGGG[G/T]ACCTGTTGGTGTGCG | 114088 |
rs770013055 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085156 | AGTTACTTCTTAAAG[C/T]GCAGGCTGCAAGCAA | 114088 |
rs770014162 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997590 | TTTGAAACACATTCA[A/G]TCATACAAATCCACG | 114088 |
rs770070020 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51076304 | CTCAAGCTGAGGGGT[C/G]ACTCTAAGGGACTGT | 114088 |
rs770084230 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047938 | GCACTCCAACCTGGG[C/T]GATACTGTGAGACCC | 114088 |
rs770106640 | snp | A/G | 1.81112e-05 | 0.0030092 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977249 | CTGTGGCTCTCGCAG[A/G]CGGAGGTAAGAACAG | 114088 |
rs770127088 | snp | C/T | 1.7172e-05 | 0.00293013 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094485 | CGGTCAATTACCCCT[C/T]CCAGTACGCGATTCT | 114088 |
rs770162139 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077615 | ACCAGGCTTGTCTCA[A/G]TCTCCTGTCCTCAGG | 114088 |
rs770169380 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979772 | ATAACAAGAGTATGA[-/T]TTTTTTGCTCCCTCC | 114088 |
rs770185000 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072657 | TTTCAATTTATTACT[-/T]TTTTTTTTTTTACTT | 114088 |
rs770265804 | snp | A/G | 1.90583e-05 | 0.00308688 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094633 | GCGGCATAGCCGGGG[A/G]AAACACGCGGACGCC | 114088 |
rs770284996 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065546 | AAGACAAATCCTGAG[C/G]TAAGTGGAAGAAGTA | 114088 |
rs770361886 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018930 | TTCTAAAATATTAGA[C/G]AGAACACATTTAAGA | 114088 |
rs770368236 | in-del | -/TA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000110 | TTAGAATAGGGAAGC[-/TA]TATAACAGGAGACCA | 114088 |
rs770409946 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030064 | TTCAACTTTTTTCCT[G/T]CATGAAGTTTTCTGG | 114088 |
rs770419114 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071004 | TAAGATAATGTAAAT[G/T]ATCCTGGAAAAAGGA | 114088 |
rs770439095 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070228 | TCATTAGATAAGCAT[C/T]GTTCAAGCATGAGTT | 114088 |
rs770460427 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020438 | ATGGGGGACAGCCAG[A/C]CACCTGTCTCTGGTT | 114088 |
rs770468867 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058553 | CATCCTCCAGGCCAT[A/C]CCCTCCCGTCATCTG | 114088 |
rs770489973 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025922 | AGTACAGCCCTGCTG[C/T]CCTAGCACATTTGTG | 114088 |
rs770524451 | snp | A/G | 0.000123434 | 0.00785504 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983465 | ATGAAACAACAACCA[A/G]GTTGATAAAAATTAC | 114088 |
rs770529737 | in-del | -/GT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002287 | CACCACGGCTGGCTG[-/GT]ATTTTTTTTTTTTCT | 114088 |
rs770541352 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008441 | ATGGGTATTACACTG[C/T]CATAAAAATGTTGTT | 114088 |
rs770552284 | in-del | -/G/GG | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096292 | AGAGGGAGGAAGGAA[-/G/GG]GGGGGGGGGAAAGGA | 114088 |
rs770575875 | snp | A/G | 1.64966e-05 | 0.00287194 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997957 | TGGAAACACTTCAGG[A/G]ATGTGGGCAGTGGTG | 114088 |
rs770606659 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991000 | TTTAAGCTTTGTTAA[C/G]TGTGGCATTAATTGC | 114088 |
rs770623565 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093149 | GGACAGGCTGAGAAG[C/G]GTGGGAAAAATTGGA | 114088 |
rs770643399 | snp | C/T | 3.59997e-05 | 0.00424247 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977273 | AGAACAGGCAGCTGG[C/T]GCCTCCACGGCACAT | 114088 |
rs770645207 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980815 | GACAGCGAATAATAC[A/C]CACTTGAATGCTATA | 114088 |
rs770670534 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024111 | AACATCATTTAAGAG[C/T]TCTCTATGCCACATG | 114088 |
rs770671698 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088281 | GCACTCTAACAGAGT[G/T]TCCAAAGTTAGACAA | 114088 |
rs770698539 | snp | C/G | 1.77827e-05 | 0.00298178 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50998033 | TCGCTCTGAGGGATA[C/G]TGCTGAAGGGCCTTA | 114088 |
rs770706533 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020845 | GCCTTTATGTCTCTC[C/T]CATATAGAAAGGCTG | 114088 |
rs770733107 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980260 | GAGATGTAGTGATTT[C/T]AAAGAACCTGCATAC | 114088 |
rs770760895 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002937 | CACAGGGTTTGGATG[A/C]AATCTTATCAAAGAG | 114088 |
rs770776435 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081620 | CCACAGGATTGCCCT[C/T]ACTTCAGATTCCAGT | 114088 |
rs770788782 | in-del | -/AAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987013 | CTTTCTATTTTGTCA[-/AAC]AATAGCTGGTTCTAT | 114088 |
rs770811386 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081818 | CCAAATGGCAGAGAC[A/G]CATGGAGTAAGGTAC | 114088 |
rs770812465 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983803 | AACTCTGCTCTCACT[A/G]TTCTATGCACTTCTA | 114088 |
rs770820772 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091833 | TTTTGTGGCAGGTAG[A/G]TATCTAAATCTCAAC | 114088 |
rs770833411 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050946 | CTGAATGCAACCTCA[C/T]GGGAGACTCCAACAG | 114088 |
rs770862761 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045745 | AATCAGATTCTTCTA[C/T]GAGCTTGATTATAAC | 114088 |
rs770879592 | snp | C/G | 1.64773e-05 | 0.00287026 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022950 | GCTTCAAACTCCACA[C/G]TGTTCTCCTGTGTAA | 114088 |
rs770881317 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073886 | TTGGCAGTTCCTCCC[A/G]TAGGATATACAGCCA | 114088 |
rs770906225 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002061 | ACTGAATAATCCCAG[G/T]TCTTCACATATAAAC | 114088 |
rs770942823 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057164 | CACCCTAAAACCCCA[A/C]AATTCTTTGGTAGAC | 114088 |
rs771028049 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995581 | ACAAAAGATGAGCAA[A/T]TTAAACCTCAGACTA | 114088 |
rs771034839 | snp | A/G | 4.9507e-05 | 0.00497504 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094165 | TGACTTCGTGGCTGG[A/G]GTGTTTGCCCTCCTC | 114088 |
rs771055049 | snp | C/T | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983123 | TGACTTGTACCTTTA[C/T]CCACATTTAGTGCTC | 114088 |
rs771077883 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044845 | CTCCCACCACTCCCT[A/G]TCATCTCCACTAAGT | 114088 |
rs771106868 | snp | A/G | 1.69049e-05 | 0.00290726 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025392 | GGAAGCCATGGAGCT[A/G]TAATCACAGGATACA | 114088 |
rs771124782 | snp | A/G | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974987 | GCCTGGTGACAGAGT[A/G]AGATTCCGTCTAAAA | 114088 |
rs771132567 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026874 | ATACTTTGTAGTTGG[A/G]TTATTGTGAGGGTTG | 114088 |
rs771135869 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51069523 | AGATTGAGAAACCCT[A/G]CTCTAGGCTGCACTG | 114088 |
rs771182118 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996308 | AGTTCTGTGACTGTG[A/G]TACCAAGGATCGCAG | 114088 |
rs771212169 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034509 | CATCACCTTCAGCAG[A/G]AGTGTGCATTGGATT | 114088 |
rs771218746 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038277 | AGGAAATGGATTCTC[C/T]TTTAGAGCATCCGGA | 114088 |
rs771229636 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061139 | GATTGTTGGCTGGGC[A/G]TGGTGGCTCACGCCT | 114088 |
rs771232548 | snp | A/G | 6.03421e-05 | 0.00549249 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094685 | GGTAGTGGGGGCGCT[A/G]GCGAACCCCCCGTAG | 114088 |
rs771281034 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006639 | ATCAGAAGTAAATTA[A/C]ATTAGACAAAGTGTT | 114088 |
rs771289585 | snp | A/C/T | 6.64092e-05 | 0.00576201 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009258 | TAAAGAGGACCACAG[A/C/T]CTAAGAAATACACCA | 114088 |
rs771289586 | snp | G/T | 1.97525e-05 | 0.00314259 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094822 | CAGACTCTGGGGTCT[G/T]CACCAGGATGTTGCG | 114088 |
rs771399062 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083932 | GGCCATCACTCAACC[C/T]CTTGAAAATAATAAT | 114088 |
rs771410360 | snp | A/G | 1.64947e-05 | 0.00287177 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010455 | GACCTGTGGTCTGGC[A/G]CAATTTCACTGTGCA | 114088 |
rs771413892 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066884 | CTTAGCTATTTATTA[C/T]AAAAGTATACTCTTA | 114088 |
rs771486123 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074816 | TTCCCTCTTACAAGG[-/C]GGCCAACAGGGCTGT | 114088 |
rs771507087 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981942 | GATCAGGGTGGTTGT[C/T]ATAGCGATCTACCGT | 114088 |
rs771523669 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027959 | AGTAAAATTGATTTG[C/G]TTACACAGAAGTGAA | 114088 |
rs771532180 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017479 | AGTGGAATATGCAAA[G/T]CATGCTCTTAATGTA | 114088 |
rs771532554 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005231 | GCTTTCCCCCTATGA[C/T]TTATAGGGGACTCTA | 114088 |
rs771547814 | snp | A/G | 1.98454e-05 | 0.00314997 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094706 | CCCCCCGTAGGAGCC[A/G]TAGCCGCTGTCCGCC | 114088 |
rs771553542 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060238 | TTTTGTAATTGGTCA[A/G]TTCTTACCACCTTAG | 114088 |
rs771570551 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020763 | GGCTTCTCATGCCTT[C/T]TGCCATTCTTTGATA | 114088 |
rs771622389 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016331 | TTTCAGATCAGCAGC[A/G]GCATTAGATTCTCAC | 114088 |
rs771685381 | snp | C/T | 2.28027e-05 | 0.00337651 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50979302 | GCTGTCAGCTTCCCT[C/T]TCTTCGGTTGGATTG | 114088 |
rs771702311 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998749 | TACAGAGGGAAGGGG[A/G]AGGAAACAGGGAAAG | 114088 |
rs771731564 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082791 | AAAAAAAAGTGACTT[C/G]TTGTTCCCATATAAG | 114088 |
rs771732042 | snp | A/G | 2.04438e-05 | 0.00319711 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094865 | ACACAAATTGTGAGA[A/G]CAGGGCAGGATGATG | 114088 |
rs771747682 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049321 | AAGATTATACCAGGT[C/T]TCACTGTGACTTGCA | 114088 |
rs771759055 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981268 | AGTTCTCTATAAGTA[C/G]AAAGCCATTCAAATT | 114088 |
rs771768873 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010031 | CCCAAGAGATATTAA[A/T]GAATAAGGACCGAAT | 114088 |
rs771800826 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014857 | CCTTGGCATCACGTA[G/T]GCAGTGGGCTGGATT | 114088 |
rs771801599 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037243 | TAAATTATCTAGATA[G/T]TAATACAGAGAGCCA | 114088 |
rs771936550 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052205 | TTAATTATCTCAATA[C/T]ATATTTTTCCAAAAT | 114088 |
rs771978458 | snp | A/C | 3.30038e-05 | 0.00406212 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025364 | GGAGAGCTGGCTCTG[A/C]AAAGACAAAGAAGGA | 114088 |
rs772009584 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048913 | GGTGTGAACCCAGGA[A/G]GCGGTGCTTGCAGTG | 114088 |
rs772038051 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062992 | ATCCATAGTTTAAAA[C/G]AAAAAAGGAAGAAAA | 114088 |
rs772063412 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991399 | ATCATTATGCCTCTC[A/G]CCTTGGATTTTGTAA | 114088 |
rs772090103 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021432 | CAAACTTCTATGACA[C/T]TGGGCACCTCTCTCC | 114088 |
rs772108756 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031785 | GAGAGCAGGGCAATC[A/T]CTGGGCAATGAGCTG | 114088 |
rs772121691 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071388 | TCTAAAAAAAAAAAG[-/AA]AAAAAAAAAAAAAAG | 114088 |
rs772135980 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075788 | CGATCTGAATTTCTC[A/G]TTGCTCTTGGCCACC | 114088 |
rs772167013 | snp | A/G | 1.64749e-05 | 0.00287005 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000791 | GCTGTTGTTGTGGGT[A/G]CAACATTCCTCCAGC | 114088 |
rs772200692 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030354 | AATGGATCCCTTCTC[C/T]GGTTTCTCTGGTGCT | 114088 |
rs772212274 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034992 | TGTAGCTATTGAAAG[A/G]GGGTAGTAACATATT | 114088 |
rs772218198 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979412 | CTGTTCAGGCTGACC[A/G]CAGGGAAGAAGAGGC | 114088 |
rs772225447 | snp | A/G | 1.64817e-05 | 0.00287064 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094197 | AAGCACTGGTAGCAC[A/G]CGGGCATCTTGCATT | 114088 |
rs772228248 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051096 | AGGTAAGGATCTTAG[A/C]TTTAACTCTAAGCAT | 114088 |
rs772230075 | snp | A/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977534 | TAACAGGCTGCTCAC[A/C]ATGGTGGGCTCTCAA | 114088 |
rs772288525 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027412 | ACCTCCCAAAGTGCT[A/G]GGATTACAGGTGTGA | 114088 |
rs772323226 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996389 | AAATAAACTGAGGCG[C/T]TACATCCTCCTGCAG | 114088 |
rs772338230 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024298 | GATTGATAAACTCCA[C/T]TGCTTTGGAAAACAG | 114088 |
rs772346202 | in-del | -/ACACAC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080441 | AGTTTTATTGAACAC[-/ACACAC]ACACACACACACACA | 114088 |
rs772355273 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072656 | GTTTCAATTTATTAC[-/TT]TTTTTTTTTTTACTT | 114088 |
rs772362989 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088438 | TTTAACTATGGAAAA[C/T]TCGTGGGAGCAGAGT | 114088 |
rs772375629 | snp | A/C/G | 8.33207e-05 | 0.00645401 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009056 | AGGATGTTGCTCTCT[A/C/G]ACTTGGGGGATGCAA | 114088 |
rs772386255 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51093384 | CTAGGAGATGCACCT[C/G]TCTGGCTTCCAGGCC | 114088 |
rs772435769 | snp | C/T | 3.29468e-05 | 0.00405861 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981955 | GTCATAGCGATCTAC[C/T]GTGAGCTCCCAGTAG | 114088 |
rs772439273 | snp | A/C/T | 4.96794e-05 | 0.00498374 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010487 | TGAGAGATCTGATCT[A/C/T]GAACCACCTAGGATT | 114088 |
rs772464435 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977719 | ATAGAGGACAGATTC[A/G]CAGAGACAGCACTTC | 114088 |
rs772500701 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995900 | TTCTAAAAAACAAAC[-/A]AAAAAAGAGATAATT | 114088 |
rs772504369 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017256 | ATACCACCTTCTATA[C/T]TAATGTTATTAATTT | 114088 |
rs772527501 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086315 | TTCCAGTTTTCTCAC[A/T]GGAAGATGTGTGGAT | 114088 |
rs772588565 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979182 | TATTAACTAGTCTGC[A/G]TCCAAGTATAAAGAA | 114088 |
rs772664151 | snp | A/G | | | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985976 | GCATTGAGAGACTGT[A/G]AAGAGGAATGCAAGC | 114088 |
rs772716456 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005999 | CCAACTGCAAACCTA[C/T]TTTCTTTTTTATCAA | 114088 |
rs772764716 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51057722 | AAATCAAAATCATGG[A/C]CTTTTAATCTGAATG | 114088 |
rs772781718 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989709 | TGTCAATGGCCAAAT[A/G]TGGTGACTCTAGGCA | 114088 |
rs772800676 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988737 | GAGAAACACTTTCCA[A/G]CTGATCCCAGCTTAA | 114088 |
rs772807284 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018773 | GTTAAATTTACCAAC[C/T]ACACATGGAAACTGA | 114088 |
rs772860244 | snp | A/G | 1.68895e-05 | 0.00290593 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094370 | CAGGCGGCACGGATC[A/G]CAGTAGAAGACATCG | 114088 |
rs772869790 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001597 | ATAAACCAGAGACTG[C/T]CTATTCTGAGAAATA | 114088 |
rs772881442 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011234 | TCTCTGAGCAAGCGG[A/T]TTCTGCTTCTAAGAA | 114088 |
rs772886719 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996285 | GTTTCATCTAGAAAA[C/T]GACCCCCAGTTCTGT | 114088 |
rs772899972 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022134 | ACTTATTGCTATGGT[C/T]TGAATATCTCTTCCA | 114088 |
rs772931647 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046155 | TTAGGGATGGGGACA[G/T]GGGTGATGGGGTGGG | 114088 |
rs772935234 | snp | A/G | | | intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983072 | ACCCCAAAAGGACTC[A/G]ATTTAAAATGCCACA | 114088 |
rs772945066 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091124 | AAATATTTGACTTAT[A/C]AGACCATTATTATTA | 114088 |
rs772972257 | in-del | -/GT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088222 | TTACTTACTAACTTA[-/GT]TTCACTAATAACTAC | 114088 |
rs773020864 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982301 | CAGACGGAGGACACA[C/T]GACCGATTCAGCAGG | 114088 |
rs773047072 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077690 | TGAGTCACCACTCCC[A/G]GCTGTCCTAAACCAA | 114088 |
rs773099404 | snp | C/T | 1.64846e-05 | 0.0028709 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981803 | GCTGCAGGGTACCTG[C/T]TGGTGTGCGAGTTGT | 114088 |
rs773141584 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079448 | TCCATGGTGGCTATA[G/T]GTCAATGGATTCTGT | 114088 |
rs773171298 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51004557 | GGGCTCCCAACCTCA[A/T]CAGGGAACACTAATC | 114088 |
rs773180633 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061097 | TGTGAAGTGTCTGCT[C/T]GAGTATTTTGTCATT | 114088 |
rs773218096 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013228 | AGTGTCTAACTTCAT[-/TT]TTTTTTTTTTTTTGC | 114088 |
rs773222995 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050224 | TTGGCTGTGTCCCCA[C/G]CCAAATCTCATCTTG | 114088 |
rs773251629 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012384 | TGTCTTTGAGATTCA[A/C]CCATGTTGTAGCATG | 114088 |
rs773267555 | snp | A/G | 3.29739e-05 | 0.00406028 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025245 | GGCGGGTTTCCTTGC[A/G]TCCCAGGTAACACCC | 114088 |
rs773293963 | snp | A/C | 1.64779e-05 | 0.00287031 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022835 | TGATGCAGCACTCAC[A/C]TTCAGCTTGTGCTCA | 114088 |
rs773294156 | in-del | -/G | 1.67217e-05 | 0.00289147 | intron-variant, frameshift-variant | TRIM9 | GRCh38.p7 | 14:50979343 | GGCAGCCTTTGAACC[-/G]GTAGCCAGCAACAGC | 114088 |
rs773383325 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51033129 | GTGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC | 114088 |
rs773423389 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995467 | AATTTGCTTTCGAAG[-/A]AAAAAACCAATCAAA | 114088 |
rs773447997 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021144 | GGGTTTCTGAAGGGT[C/G]CTCAGATTGAAGGGC | 114088 |
rs773463523 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067644 | ATCTTTGCATGTGCT[A/G]TTTCATCTGTTCGGC | 114088 |
rs773499011 | snp | A/G | 4.96816e-05 | 0.00498381 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025374 | CTCTGCAAAGACAAA[A/G]AAGGAAGCCATGGAG | 114088 |
rs773499769 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998668 | TATGTTTAGAACTCC[A/G]CTGATAACTTCAGAA | 114088 |
rs773512455 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060530 | GGAGTGCAGTGGCAC[A/G]ATCTCGGCTGACTGC | 114088 |
rs773531886 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993805 | CTAATGTTAGCACCA[C/T]AGCGGACTGTGCTGA | 114088 |
rs773533550 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054577 | CATTGCCGCCGGCCA[A/T]TGCTCTTTTTTGTTT | 114088 |
rs773555154 | snp | C/G | 1.72487e-05 | 0.00293667 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094494 | ACCCCTTCCAGTACG[C/G]GATTCTTGGGGAAGC | 114088 |
rs773556667 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985641 | CCAGCGCCCGTGCCG[G/T]GCTATGCCACTGCAT | 114088 |
rs773559159 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052613 | ATGATATGAGCCTCT[G/T]ATTTAAAGTAGGAAT | 114088 |
rs773564204 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976818 | ACATTCTAGCAGGTA[A/G]GCTGTATGCTACAAA | 114088 |
rs773587840 | snp | A/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997745 | ATACATTTGTCTTAC[A/C]CACCAGGGGCACATT | 114088 |
rs773590642 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083063 | CCCTCAGTTAACACA[C/T]AGAAATTACTTAGAT | 114088 |
rs773611305 | snp | G/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095150 | GCGCCAGCCCGGACC[G/T]CCCCTACCTGCCCTC | 114088 |
rs773613104 | snp | C/T | 1.65455e-05 | 0.00287619 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009243 | AGAAATCTAATCAGA[C/T]AAAGAGGACCACAGC | 114088 |
rs773621543 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065559 | AGCTAAGTGGAAGAA[A/G]TAAGGACACACATTT | 114088 |
rs773663546 | snp | A/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978395 | GCACAGCTCTTCCCC[A/C]ATGCATGGCTCTGGT | 114088 |
rs773668620 | snp | C/T | 1.64898e-05 | 0.00287135 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009099 | CACTTGCACGAAATC[C/T]AGCTGGTGGATGGAT | 114088 |
rs773687271 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037202 | CATTCTAAATAACTC[C/T]GAGATCAAATAGGAA | 114088 |
rs773718787 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980056 | AAGAAGCACTTTTGT[C/T]GCACCTAAACCACAT | 114088 |
rs773731555 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019731 | GTGCTTTGCAATGCC[C/T]TATGAGGTACCACTT | 114088 |
rs773734290 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095962 | CCTTCTTCCTCCTCG[A/C]GGCCTCCCAAAGCAC | 114088 |
rs773738892 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052753 | GACTCCAGACACAGA[C/T]GTCATTGCCCATAAA | 114088 |
rs773749972 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51030210 | GTGAAGTGGGAATTA[A/G]GTAAAGGAAGGAGAC | 114088 |
rs773799850 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51012833 | AGCATCTTTTCATAC[A/G]TTTATCGGCTGTTTG | 114088 |
rs773840685 | snp | A/G | 3.51327e-05 | 0.00419108 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997967 | TCAGGAATGTGGGCA[A/G]TGGTGGGGTTACCTC | 114088 |
rs773843605 | in-del | -/AAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003511 | TACAATGTCTCTGAT[-/AAG]AAACTCAAATGTACC | 114088 |
rs773847322 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007406 | AAAGAATTTCTGCAA[C/T]AAAAATGTAGATTTG | 114088 |
rs773949401 | snp | C/T | 1.75456e-05 | 0.00296184 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094518 | GGGAAGCCGCGGAGC[C/T]CCCGGTCATCCAGGA | 114088 |
rs773954539 | snp | A/G | 1.64963e-05 | 0.00287192 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979517 | TCGAGGAGGACCCCA[A/G]TTGTGGCCCCTTTTG | 114088 |
rs773964879 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081200 | AAGACTTTAAATAGA[C/T]ATTTCTCTTAAAAAA | 114088 |
rs774013214 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072427 | AACAGACTGCATCCA[C/G]GTATCTAAATATAAA | 114088 |
rs774018282 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042300 | CTCCATTTTGTGCAC[C/T]TCCCTTGTCCCCTCA | 114088 |
rs774029244 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991023 | TTAATTGCAATTGAG[A/G]AGTGAGAAACAAATC | 114088 |
rs774050444 | snp | C/T | 3.29544e-05 | 0.00405908 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022951 | CTTCAAACTCCACAC[C/T]GTTCTCCTGTGTAAC | 114088 |
rs774073973 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022671 | AAGGAGCAGGTAGTG[A/C]ATGAAGGGAGGTGTC | 114088 |
rs774133649 | in-del | -/CACATTTTAAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009681 | GCACATGGAATTTCT[-/CACATTTTAAG]CACATCATCTTCATG | 114088 |
rs774155730 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088361 | TGTATACATAGGCAT[A/G]TTGATACAATATACA | 114088 |
rs774175164 | snp | C/T | 0.000372001 | 0.0136331 | intron-variant | TRIM9 | GRCh38.p7 | 14:50983471 | CAACAACCAGGTTGA[C/T]AAAAATTACTTGTAT | 114088 |
rs774180869 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013861 | ATTAAAGAGAGGTGA[C/T]CTACAGCTAATATGC | 114088 |
rs774215486 | in-del | -/A | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096304 | GGAAGGGGGGGGGAA[-/A]GGAAAGGCGGAAGGA | 114088 |
rs774279758 | snp | A/G | 5.20215e-05 | 0.00509981 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025394 | AAGCCATGGAGCTGT[A/G]ATCACAGGATACACC | 114088 |
rs774352391 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050978 | ACCACCAAGCCAAGC[C/T]AAGATGCTGCTGATT | 114088 |
rs774361616 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51029776 | CCGAGAGGATACCCC[-/T]TGAGTGAAGGTTTCA | 114088 |
rs774363903 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995661 | TTTCTGTGATACAGA[A/G]TTTTTGTTTTGAAGT | 114088 |
rs774364540 | snp | A/G | 1.65056e-05 | 0.00287272 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025233 | TACGTATTAACCGGC[A/G]GGTTTCCTTGCGTCC | 114088 |
rs774373790 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062905 | TTTATAGATACCTTG[A/G]AATTTCCAAAATCCA | 114088 |
rs774380200 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034587 | AATTTGAAAGTTTAA[C/T]GCAGTTTCACCTCGG | 114088 |
rs774384374 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022324 | AAGTTTGGCTCTTAT[C/T]CTCTCATTTCCCATG | 114088 |
rs774408499 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983845 | GCCAAAAGGTCTTCA[C/T]TGTGACTTGAGCCCA | 114088 |
rs774460119 | in-del | -/TTTTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077388 | CATCTCCAATTCTGT[-/TTTTTTTTTTT]TTTTTTTTTTTTGAG | 114088 |
rs774529312 | snp | G/T | 1.64898e-05 | 0.00287135 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094167 | ACTTCGTGGCTGGAG[G/T]GTTTGCCCTCCTCCA | 114088 |
rs774535294 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073925 | ACAACAAGCAGTGGT[A/G]TGCTGGGGCTGGCTT | 114088 |
rs774602054 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005940 | AACTTTAGATAGTGC[A/G]TTCTTGCTGAATAGC | 114088 |
rs774618344 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048800 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 114088 |
rs774624598 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026070 | CTCTTCCAGCCTCCT[C/T]GTCCGCTGGGGAGGC | 114088 |
rs774635096 | snp | C/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096412 | TGAAATAGTACATAG[C/T]CGGCTTTTGCTGAAT | 114088 |
rs774658420 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044976 | CCTTAGGGTTGGTGA[C/G]GATGGTGTTGAACTG | 114088 |
rs774664273 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51061249 | GAAACCCTGTCTCTA[C/T]GAAAAATATAAAAGT | 114088 |
rs774682840 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053159 | GAGAGACCCTGTTTC[-/A]AAAAAAAAAAAAAAG | 114088 |
rs774709822 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047605 | TTGCAAGGCAGTGAT[-/C]CAGACTCTGCAGTAC | 114088 |
rs774741667 | snp | A/G | 1.64972e-05 | 0.00287199 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010458 | CTGTGGTCTGGCGCA[A/G]TTTCACTGTGCAGTG | 114088 |
rs774756965 | in-del | -/AC | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999366 | TTTTACACACACACA[-/AC]ACACACACACACACT | 114088 |
rs774789037 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026938 | TAAGGGAACAATTCT[G/T]AATTCTGAAATGCTG | 114088 |
rs774812021 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089876 | CATTGACTCTGTTTG[A/T]CATGAATGTTTATGG | 114088 |
rs774825828 | snp | G/T | 1.64765e-05 | 0.00287019 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981818 | TTGGTGTGCGAGTTG[G/T]TGTGCATGAACCAGC | 114088 |
rs774847946 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51083989 | TCACATCAAATAATG[A/T]ATGGCAAGTAAACAA | 114088 |
rs774867958 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981947 | GGGTGGTTGTCATAG[C/T]GATCTACCGTGAGCT | 114088 |
rs774903608 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981408 | TCCCACAAGGAAAAA[-/T]TTTATTGTACTAATT | 114088 |
rs774906936 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977707 | CCAAATCCATGGATA[A/G]AGGACAGATTCGCAG | 114088 |
rs774932047 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068141 | TTGTATTTTTAACAA[A/G]TTCCCAGGTGATGGT | 114088 |
rs774967376 | snp | A/G | 2.06383e-05 | 0.00321228 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094870 | AATTGTGAGAGCAGG[A/G]CAGGATGATGGGCTC | 114088 |
rs775043965 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048065 | TTAATAGCTTGCTCC[A/G]AGGTGCCATTTCTTA | 114088 |
rs775050694 | snp | A/G | 1.98179e-05 | 0.00314778 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094712 | GTAGGAGCCATAGCC[A/G]CTGTCCGCCTCGCTG | 114088 |
rs775057160 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998766 | GGAAACAGGGAAAGG[A/G]GGAAGAATGACATTT | 114088 |
rs775068985 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51008764 | AATATTTCTGGATTC[A/C]TTTCTGTACCAAGAT | 114088 |
rs775103665 | snp | A/T | 6.66134e-05 | 0.00577081 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010335 | AAGCATCCTAGACTA[A/T]GTCCTATGGGACATT | 114088 |
rs775164904 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038313 | ACTCAGCCCTGTTTG[C/T]TGGACTTCTGACCTA | 114088 |
rs775196484 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070658 | TTCCAGATTTTGTAG[A/C]ATTTTGGATTAAGAA | 114088 |
rs775254742 | snp | C/T | 1.64879e-05 | 0.00287118 | intron-variant | TRIM9 | GRCh38.p7 | 14:51025242 | ACCGGCGGGTTTCCT[C/T]GCGTCCCAGGTAACA | 114088 |
rs775264549 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065851 | GCCCACTTGAAGAGG[A/G]TGCTTTGACATTTAT | 114088 |
rs775277100 | in-del | -/TTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51001229 | AAGCTGTGCTAATAA[-/TTT]TTTTTTTTTTTTTTT | 114088 |
rs775285285 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077772 | TATGAAATCACATCT[C/T]ATAGCATAGTTCATA | 114088 |
rs775289677 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003229 | TTAACATATTTACTA[C/T]GGAAGATAAATATAA | 114088 |
rs775333987 | in-del | -/CAA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006012 | TACTTTCTTTTTTAT[-/CAA]CAACAACAACAAAAA | 114088 |
rs775335593 | snp | C/T | 0.000161121 | 0.00897412 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977281 | CAGCTGGCGCCTCCA[C/T]GGCACATCCTTAGGC | 114088 |
rs775348198 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980361 | ACGATCAGATTTGTC[G/T]TTCCCATTTTTTTGA | 114088 |
rs775368307 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049949 | TGGAGGGGTTGGGTG[C/T]ATTAAGAGTGGAAAG | 114088 |
rs775445983 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023344 | GGCATTGCTGAGGCA[C/T]GAGAAATCATTAAAT | 114088 |
rs775468272 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981296 | ATTGGCATCCATAAG[C/G]TTTAGTTTAATGAAT | 114088 |
rs775515986 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092696 | ATCTCCTCAAGAGTT[C/G]CTCCCTTCCTTCTAA | 114088 |
rs775523243 | snp | A/G | 3.33356e-05 | 0.00408248 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998073 | GTTTGGAGGACCAGG[A/G]TCTTGCTGTACGGGC | 114088 |
rs775527354 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071097 | CTAAGAAAGTGGAGG[C/T]GGCCAGGCACAGGGC | 114088 |
rs775541383 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013114 | TTCCAGTGTCCCAAA[C/G]GGTTCCCCCTGTGTT | 114088 |
rs775631531 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024300 | TTGATAAACTCCATT[C/G]CTTTGGAAAACAGAA | 114088 |
rs775652122 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035908 | GAATACCCACAGAAA[A/G]GCATGCTCCCTGACA | 114088 |
rs775705609 | in-del | -/TT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999041 | CAGTGCTTCTCAAAC[-/TT]TACGTGCATATGAAT | 114088 |
rs775705971 | snp | A/G | 4.9476e-05 | 0.00497348 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000731 | CAGAATGTATCCATC[A/G]GCGGGCACCGTGGAC | 114088 |
rs775730775 | snp | A/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50996402 | CGCTACATCCTCCTG[A/C]AGGATGAAACGAGAG | 114088 |
rs775735428 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014027 | CCCTTGACTACAGGT[A/T]CTGGAAGTCCGAATA | 114088 |
rs775757427 | snp | A/G | 1.64749e-05 | 0.00287005 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000793 | TGTTGTTGTGGGTAC[A/G]ACATTCCTCCAGCTG | 114088 |
rs775773944 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979242 | AGTTGCCAGTGCTGA[C/T]CCCTTTCTCTCCTCC | 114088 |
rs775784102 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040990 | AGTGTTGAAAGGCTT[A/C]TTAGGATTCAGTACT | 114088 |
rs775807484 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051212 | CTATAGGAAACCTTC[A/G]TTGTTCCTGAAAATT | 114088 |
rs775820617 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010220 | CGGGAAGTCAGTGGA[A/G]TTTATTTAGCCGGCA | 114088 |
rs775825832 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979417 | CAGGCTGACCGCAGG[A/G]AAGAAGAGGCCCTCC | 114088 |
rs775865136 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086344 | ATTATGAAGATTAAA[C/T]GAGAAAATGCTGTAA | 114088 |
rs775894901 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995931 | ATTTGATCCTATAGG[C/T]TTTGTCTATTGTTAC | 114088 |
rs775925767 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018028 | AATCATAATTGTGGT[G/T]AAATAATTAGAATTG | 114088 |
rs775950396 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989620 | CATATTTCATCACAC[A/G]CAGGGATCCCGTGTG | 114088 |
rs775962027 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074864 | TCCAAGGCATAGGTA[A/G]AATGAGGGGAATGAA | 114088 |
rs775965033 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070324 | AACAGAAACATACAT[A/G]AAACAAGTTTATGCA | 114088 |
rs775972066 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045992 | AACAAACGAACCAGT[A/G]CAACACACATTGACG | 114088 |
rs775978836 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074093 | ACTGAATAATAGTAA[A/T]GATCATAACAACGAA | 114088 |
rs775996005 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999829 | AAGTAGGGTGGCAGG[C/G]AGAGGATGGATGAGA | 114088 |
rs776061631 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045081 | ATCAAATACTGCATA[C/G]TCTGACATTGTCGGG | 114088 |
rs776068667 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005350 | AGGTGAGTAGAGGCA[C/T]TTAAGGGGATTAACA | 114088 |
rs776086784 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039677 | TGAGTGGTGGTTACA[C/T]GAATAATTTTTTTTA | 114088 |
rs776106758 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046433 | CTGTACTATGGTTTT[A/G]CAAAATGCTACCACT | 114088 |
rs776181517 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067251 | CCTCCTAATAGTCAT[C/T]CTTGATTTCTCTCTT | 114088 |
rs776192850 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988403 | CCCTTTATAGGGTGG[A/G]GACTGAGGGTAGCTA | 114088 |
rs776195727 | snp | A/C | 1.67539e-05 | 0.00289425 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010511 | TAGGATTAAAAAAAA[A/C]ACAACAGAACAGTCC | 114088 |
rs776216649 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028205 | TTGTGTTTATGGTCC[A/G]TCCCAAGAATGCCTT | 114088 |
rs776221330 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50981328 | GTAATAAGAAGAATG[G/T]CTACTATTTTCAGGT | 114088 |
rs776240363 | in-del | -/AAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000478 | CATGTCCTGTCTCAT[-/AAG]AAGGGTAGGGCAGTT | 114088 |
rs776248669 | snp | G/T | 1.64738e-05 | 0.00286995 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981972 | TGAGCTCCCAGTAGT[G/T]GATGCCCTTGGAGAA | 114088 |
rs776289251 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011212 | TGCTTTAACCTAAAT[A/G]GGCATCTCTCTGAGC | 114088 |
rs776293729 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068564 | AGTTATTTTTATCCC[C/T]GTTTTACAGATGACA | 114088 |
rs776301186 | snp | A/G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032028 | CCCATTCTTTGTTGT[A/G/T]AGACTTGCATGCCCA | 114088 |
rs776369784 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055893 | AATATTTATGTTTTA[C/T]TAGATATATAAATTC | 114088 |
rs776428307 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992490 | AGGCAGGAGGATCAC[C/T]TGAGCCCAGGAGGTC | 114088 |
rs776444573 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005123 | AAAGATAACCCTGAA[C/T]GCAGGTTTTGAGTCC | 114088 |
rs776519527 | in-del | -/AGGGGT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025798 | GAACAGGATGAAGGA[-/AGGGGT]AGGTACTGGTGTGAT | 114088 |
rs776560352 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020930 | AAAAAGTGCCAGGAA[A/G]TGTTCGCAATGTTTC | 114088 |
rs776567599 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049431 | ACTACAGGGCTGCCA[C/G]GATTGCTCAGCACAA | 114088 |
rs776608948 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51072198 | CCAGGAAATGTATTT[A/C]TTTTTTTTCATAGGG | 114088 |
rs776625094 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077998 | AACGACCCAATTGAG[C/G]AACCAAGTAAACCTG | 114088 |
rs776664175 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021832 | ATGTCTCCTGGAGGA[C/G]CAGTCCTGCCAATAG | 114088 |
rs776672615 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075279 | GGAGCCCCACTCCCA[C/T]GCCTACTCCACGTTA | 114088 |
rs776675030 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003303 | AATGATTCCCCCCGG[C/G]GGGTATTTATTCTTA | 114088 |
rs776675763 | snp | A/G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043468 | AGTGCTGAAATGCCT[A/G/T]TTGGCCCCATAAACA | 114088 |
rs776696007 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027328 | TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCTCC | 114088 |
rs776713412 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010624 | ACTAAATTTATGAGA[A/G]TATTTTCTGGCAGTG | 114088 |
rs776727075 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51077339 | GAGGTAAGGCGACCA[G/T]GAGCTGTCAAACTTA | 114088 |
rs776755620 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010330 | GACTTAAGCATCCTA[A/G]ACTATGTCCTATGGG | 114088 |
rs776759091 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51052490 | TGTTGTTGCTATTAG[C/T]GTCATTTAATTTATG | 114088 |
rs776787031 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025853 | ATAATCACAAATTCA[A/G]TGGGCAGGATGACAT | 114088 |
rs776849333 | snp | C/T | 1.64887e-05 | 0.00287125 | intron-variant | TRIM9 | GRCh38.p7 | 14:51022984 | AGCACATTTCTCAAC[C/T]GCAAGCTGCTGGGTG | 114088 |
rs776882822 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985441 | GGATTGCCTGCTTTA[C/T]AGGATGCTTTCTGCT | 114088 |
rs776911357 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51087954 | TACATTAATATTCCT[C/G]ATGCCTAAAATCATT | 114088 |
rs776931527 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976412 | TTTATTTTTGCTTTT[C/T]CTCCTACTGGAATAT | 114088 |
rs776964845 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991166 | ATAAGGAACTATCAT[C/G]AGAGGAACTGAAAAT | 114088 |
rs776966255 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51024577 | TTACTGTCTTATACA[A/G]TTTATGGTTTTTCTC | 114088 |
rs776977985 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51049173 | TTTAAGTGATTCTCC[C/T]GCCTCAGCCTCCTGA | 114088 |
rs776987772 | snp | A/T | 0.000122003 | 0.0078094 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50983383 | AGGTATACTTGCCTA[A/T]TTGAGAGTAAGGTGC | 114088 |
rs777005174 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041804 | GCCTAATATGATGTT[-/AA]AAGTGTTTCAAATAA | 114088 |
rs777017526 | snp | C/T | 3.40304e-05 | 0.00412481 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094459 | GGGCCGCGGCTTTGC[C/T]CTGCTGGTAGCGGTC | 114088 |
rs777057030 | snp | C/G | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976793 | CTACAGGAGAGGTAA[C/G]AGGGTAAGAACATTC | 114088 |
rs777061473 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51007149 | GCCCCCTCACTGAGG[C/T]TAATTGGGTTAGCTC | 114088 |
rs777095158 | in-del | -/TG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002108 | GGAACCATGGTTTTG[-/TG]TGTGTGTGTGTGTGT | 114088 |
rs777145632 | in-del | -/CTTTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027132 | AATGCTGGCTGTTAA[-/CTTTTTTTTT]TTTTTTTTTTTTTTT | 114088 |
rs777154602 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011117 | CGGATGCAGAATTAA[A/G]TTTTAAGAATAACCC | 114088 |
rs777157344 | snp | C/T | 1.6955e-05 | 0.00291157 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094359 | GGGTGGCAGCGCAGG[C/T]GGCACGGATCGCAGT | 114088 |
rs777158517 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091988 | GGATAGGCTTGTCAT[-/A]AAAAAAATAATAATG | 114088 |
rs777174127 | in-del | -/T | 3.86533e-05 | 0.00439604 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977399 | CATCGTGCATCCCCC[-/T]GTCCCTTTACACAGT | 114088 |
rs777191635 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035076 | GATAGCAATAGATAT[A/G]TGACATGACAAATTT | 114088 |
rs777239315 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048983 | ATGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 114088 |
rs777251993 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983992 | ACAAGATCCTTCTCA[A/C]CTGAGGGAGGGGAGG | 114088 |
rs777295762 | snp | A/G | 1.64768e-05 | 0.00287021 | missense, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000816 | TCCAGCTGTAGGATA[A/G]GGGTTGCTGGGACTG | 114088 |
rs777308512 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041915 | TGGTATAAAATTAAT[A/G]AACTGAATTCCATGT | 114088 |
rs777309108 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51081777 | ATATTTACTGGTTTA[C/T]TATGGAGGATACAAC | 114088 |
rs777352138 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002903 | TTAGGAGAAGAAATC[A/G]TGTTTTAAGCTTCAA | 114088 |
rs777361081 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000782 | CAACGTAGCGCTGTT[A/G]TTGTGGGTACAACAT | 114088 |
rs777444013 | snp | C/T | | | downstream-variant-500B | TRIM9 | GRCh38.p7 | 14:50974828 | AACATGGTGAAACCC[C/T]GTCTCTAATAAAAAT | 114088 |
rs777537988 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092951 | ATGCAGGTAAGTGAC[C/T]CATTCGGATCTCAGG | 114088 |
rs777562010 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046863 | ATGTACAATGTTTTC[A/G]ACAGTGCTTGGCATA | 114088 |
rs777562168 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034350 | GCAATAAGAAGTTTT[G/T]GAAAAAGGGTCCCTT | 114088 |
rs777567198 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995924 | GATAATTATTTGATC[C/T]TATAGGCTTTGTCTA | 114088 |
rs777591122 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075459 | TACATTTGAAAATTA[C/T]ATACCAAAGATTTGT | 114088 |
rs777596166 | snp | A/G | 6.5912e-05 | 0.00574035 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025337 | CCTGTCTGACAGTCC[A/G]TTCAGCGCCTGGGAG | 114088 |
rs777620530 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023077 | GTCCACAATGCACAT[C/T]TGGTAATTTTAAAAA | 114088 |
rs777627008 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51003760 | GGAAAAAAAAAAGAA[A/G]GAACTAACCCAGAGA | 114088 |
rs777640244 | snp | A/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997122 | GGGTGATTTCTTTGA[A/T]TAAAATGACACCCCA | 114088 |
rs777645058 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51006606 | AAGCATATAAATTAA[A/C]CAGGCAGAGTGATAA | 114088 |
rs777661182 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074608 | GGCCTTTTAATTACT[C/G]TTTGATCCTTCCACC | 114088 |
rs777662119 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092966 | CCATTCGGATCTCAG[C/G]TAACTGGGGAAGAGA | 114088 |
rs777669021 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989130 | CTTTTCTGGGCTAAA[C/T]AGAGTCAATGTCCAA | 114088 |
rs777734792 | in-del | -/TTTTTTTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027135 | GCTGGCTGTTAACTT[-/TTTTTTTT]TTTTTTTTTTTTTTT | 114088 |
rs777759588 | snp | A/G | | | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976925 | AATTTTCTCCTGGCG[A/G]TGCCAGTCCAGTAAG | 114088 |
rs777760204 | snp | A/G | 1.78624e-05 | 0.00298846 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094965 | CTGGGAGGAGACAGC[A/G]ACGGCTGCAGCGGGT | 114088 |
rs777777491 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51068233 | GCACTATGCCAGGAC[C/T]GTGGGGATGAAAAAG | 114088 |
rs777784536 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050736 | TCCCTCACTCTCTCT[A/G]TTTTTCCCTCCATCC | 114088 |
rs777826123 | snp | A/C | 1.64808e-05 | 0.00287057 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50982033 | ATAGCTACTACAGGT[A/C]ACTGTCAGGTTGTCA | 114088 |
rs777841431 | snp | C/T | 3.29652e-05 | 0.00405974 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51010420 | ATTTTCCTTAATCAC[C/T]TCCAAGCAGTACTCC | 114088 |
rs777858952 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51085189 | TAAGAGTAAGAGGAG[A/G]TGAGCAAAAACCTCA | 114088 |
rs777862991 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978886 | TATTCTATAATAAAT[A/G]ATAATTGACTAAGTT | 114088 |
rs777865548 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50977552 | GGTGGGCTCTCAAAT[C/T]CTGGTGACATTTGAT | 114088 |
rs777874237 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51062751 | TGCTTGGCTAATCCC[C/T]GAACTGTGGATGCAT | 114088 |
rs777896462 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005844 | AAAAAAGGTACCAGC[C/G]TTCTCCAGATTGATC | 114088 |
rs777900073 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51016738 | CCATGGAAAACAACT[A/G]TCTTCCATGAAACTG | 114088 |
rs777934624 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045665 | TCTTTAATACCTTCA[C/T]TAAAAGTGAGAGGGC | 114088 |
rs777974936 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055355 | GTGTGTGGTAGGTAG[A/C]ATAATGGCACCCCAA | 114088 |
rs777988685 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017222 | ATAGTTTAAGGCAAA[G/T]ATTTTCCCCGTTCTC | 114088 |
rs778008600 | snp | C/T | 1.75644e-05 | 0.00296342 | missense, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977338 | CGGGGACTGGGAGCC[C/T]GGTGTGCAGCGTGAC | 114088 |
rs778038532 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51086099 | GTAATTTTCATATAC[A/G]AGAACTAAAGGAGTC | 114088 |
rs778147878 | snp | G/T | 3.87687e-05 | 0.0044026 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094646 | GGGAAACACGCGGAC[G/T]CCGTTGGGGGACTTC | 114088 |
rs778166051 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060639 | GCCCGGCTAATTTTT[C/T]TGTATTTTTAGTAGA | 114088 |
rs778217627 | snp | C/G | 1.64849e-05 | 0.00287092 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51025355 | CAGCGCCTGGGAGAG[C/G]TGGCTCTGCAAAGAC | 114088 |
rs778225290 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000408 | ATTAGGCATTGTCCA[C/T]ATAGCTAGGGTGGAG | 114088 |
rs778245459 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982617 | AAAGCTCACAAGCTG[C/T]GAAGCTATAAGCAAC | 114088 |
rs778270667 | snp | G/T | 3.93437e-05 | 0.00443512 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094815 | GGGGATTCAGACTCT[G/T]GGGTCTGCACCAGGA | 114088 |
rs778283812 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066750 | GAGGTGCAGAAAACG[A/G]AAGTGAGGTATAGAG | 114088 |
rs778297992 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51039054 | CTGGGAAATGTTAAT[C/T]ACAAGATCTGAATTT | 114088 |
rs778312286 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50988225 | AGGACATATAAAATA[A/G]TATGAATTTCAGAGT | 114088 |
rs778340210 | snp | C/T | 0.000101254 | 0.00711454 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50998057 | GGCCTTACCCTCAGA[C/T]GTTTGGAGGACCAGG | 114088 |
rs778451760 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078973 | AGTAACCATTTTTCT[A/G]TCTGTATCCCATAAC | 114088 |
rs778466609 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060139 | GTTGTTTCTTTCCAC[A/G]GACTGTAGTTGGCTT | 114088 |
rs778475295 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032633 | CCTCACTTCCAGGTG[G/T]ATCTACCAAGAGCAC | 114088 |
rs778509225 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992203 | CTGACAGGTTCTTTG[A/T]TCCTCACAAGGTGAC | 114088 |
rs778529295 | in-del | -/GAAG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066057 | CATCTCTTTTAGAAG[-/GAAG]GAAGGAAGGAAGGAA | 114088 |
rs778552991 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51064977 | CTGGCTCCTCACTTT[C/G]GGCCACTGCAGCAGG | 114088 |
rs778574710 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043058 | TGTATACATGATATA[C/G]TGTTTCTTCCTCTGA | 114088 |
rs778662641 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025551 | AGTAGTTTCTCCTTG[A/G]AAGCAGTGAACACTT | 114088 |
rs778663711 | snp | C/T | 1.66158e-05 | 0.0028823 | intron-variant | TRIM9 | GRCh38.p7 | 14:50998229 | GCACTTAGCCTGCCC[C/T]CTTCTGAGGGGCGAG | 114088 |
rs778686048 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981883 | GTCGTCTTTTCCTAA[C/T]ATCACATCCTTCATC | 114088 |
rs778689175 | snp | C/T | 9.97075e-05 | 0.00706002 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981754 | GGCTCTCACTCCTGA[C/T]CAGAAGCCAACGTGA | 114088 |
rs778692039 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50976352 | CATGAGTCTCTTTGA[C/T]CCTTGCCCATTTCCT | 114088 |
rs778723314 | snp | C/T | | | | | GRCh38.p7 | 14:50985074 | GAAATATGAAATGTG[C/T]ATCATGTGTATCCAT | 114088 |
rs778755202 | snp | A/G | | | | | GRCh38.p7 | 14:51014831 | CTTTGGCTCTGATGT[A/G]CCAGAGAACCCCTTG | 114088 |
rs778776991 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993015 | CAGGCAGGGCTGGAA[A/T]GCTTCTGTGAATAAA | 114088 |
rs778779990 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50986403 | TTAGTGGTAGAAAAT[A/T]GGAAGGTTTCCTTTT | 114088 |
rs778797300 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051301 | AGAGCTCAAAAGACA[C/G]AGATTGAAAAGAGAG | 114088 |
rs778798260 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019337 | GCATTAGTTCACCAC[A/G]TTCTGAAAATAGATA | 114088 |
rs778823086 | in-del | -/G | 3.34641e-05 | 0.00409035 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010510 | TAGGATTAAAAAAAA[-/G]AACAACAGAACAGTC | 114088 |
rs778823999 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51051935 | TTATGCCACTGCACT[A/C]CAGCCTAGGCAACAG | 114088 |
rs778824636 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046930 | TGAACATTATAAAGT[C/T]TGAAACAGGTGGTAC | 114088 |
rs778829354 | snp | A/C | 1.65836e-05 | 0.0028795 | intron-variant | TRIM9 | GRCh38.p7 | 14:50981770 | CAGAAGCCAACGTGA[A/C]GAAGGCTTGGTTTGG | 114088 |
rs778831584 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51063757 | TCCTTCAAAAATTAA[C/T]GGAAAAGAAAGACAT | 114088 |
rs778888851 | snp | C/T | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095398 | ATGATTCATCCTCGC[C/T]CGGCTTACTTCCGAC | 114088 |
rs778914169 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979707 | ATAAATTTTAATACC[A/G]CAGATATACTGTATA | 114088 |
rs778956918 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51042010 | GCAGGAAGCTCTGTC[A/G]GAGTGAGGTGGCATC | 114088 |
rs778967440 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51020097 | CTCAGAGAACTCAGC[C/T]AAAGGGAAGCGGAAG | 114088 |
rs778967598 | snp | A/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997284 | CATCTGAGACACATT[A/G]CTTGTCTTTGATGAC | 114088 |
rs779013555 | in-del | -/TA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51082530 | AAAGGCCACATATTT[-/TA]TGATTCCATTTATAT | 114088 |
rs779026735 | snp | C/G | 3.66522e-05 | 0.00428074 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982150 | AGACAGACCCAACAA[C/G]CTCAGCACCATAACA | 114088 |
rs779035282 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074745 | CAGAGCTCAAAGCTG[G/T]TCAGTGTGTGTTCTC | 114088 |
rs779078594 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51018599 | TGATAATTATTCTAA[C/G]AAAACTCATAGATTA | 114088 |
rs779094451 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000521 | CTCCATCCACCTTCA[C/T]GGTAGAGGGAGAAAG | 114088 |
rs779136984 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51075657 | AATTGTTTGCAGACT[C/T]CCAGAGGTGAGTGAG | 114088 |
rs779137913 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027974 | GTTACACAGAAGTGA[A/C]GCTGCCTGGTGTCTT | 114088 |
rs779164511 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011829 | TCAGACTTATTTATC[A/G]TTGCAGTCATTGTAT | 114088 |
rs779193293 | snp | G/T | 0.000105725 | 0.00726989 | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094978 | GCGACGGCTGCAGCG[G/T]GTGCCTGAGCTGGCG | 114088 |
rs779250823 | snp | C/G | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50997209 | TGTGTCTTGCTTACT[C/G]TTAAAATGAAAATGT | 114088 |
rs779266217 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050518 | TACCCAGTCTTGTGT[A/G]TGTCTTTATCAGCAG | 114088 |
rs779366827 | snp | A/G | 1.66685e-05 | 0.00288686 | intron-variant | TRIM9 | GRCh38.p7 | 14:51000632 | CCTGGCAGGTCCTCT[A/G]ACAGAGTCACTGCTT | 114088 |
rs779374435 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51002430 | TGAGCCACCGTGCCC[A/G]GCTGGGAACCATGTT | 114088 |
rs779389707 | in-del | -/TGG | 1.94539e-05 | 0.00311875 | cds-indel, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094791 | GAGCCCGCGGCCCGA[-/TGG]CTCTGGGGGGATTCA | 114088 |
rs779404291 | snp | C/T | 2.84451e-05 | 0.00377117 | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979289 | GTCTGGGCCTTACGC[C/T]GTCAGCTTCCCTCTC | 114088 |
rs779429773 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50985323 | TTCTAATTCGGCTAG[C/T]AGTGATCCCACCCCA | 114088 |
rs779458610 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080783 | GATATTATACTGAGG[C/T]AGACTCCGTTTCCAA | 114088 |
rs779466178 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50989511 | ATGTTTCAGGTCACA[A/G]CTAATATGCAGGATA | 114088 |
rs779474155 | snp | G/T | 4.95454e-05 | 0.00497697 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094256 | CTCGTGGTCTGTGCA[G/T]GTGGAGACCTTGCGT | 114088 |
rs779494291 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51025750 | TAGCACAAAGGGCTA[C/T]TGGTCTGGGTAGGGC | 114088 |
rs779559534 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091616 | GTGGGGGAGTAATGT[G/T]TGTTGTTCATCTAAC | 114088 |
rs779566139 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005548 | GGTATCTGAAATCTA[C/T]TCTCAACCAAACAGT | 114088 |
rs779597108 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon, intron-variant, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51000764 | AGGTGGCTGTTTCCA[A/G]GACAACGTAGCGCTG | 114088 |
rs779597990 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060680 | CGCCGTGTTAGCCAG[C/G]ATGGTCTCGATCTAC | 114088 |
rs779609188 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060280 | AAGTCTTATATCAGC[C/T]TAACTTCCTATGACC | 114088 |
rs779664395 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51031938 | GTGAACCTGACTCTA[C/T]GAGCTGTGTGGAGGG | 114088 |
rs779684658 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054976 | CTGGGACAACAAGCG[C/T]GCGCCACCAGGCCCA | 114088 |
rs779694068 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021594 | GCCAGCACTATGAGC[A/G]TAAGACCAGACCTCA | 114088 |
rs779794483 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011070 | GGAGCTTGGGAGAGG[C/T]AATGAGCTAATGAAA | 114088 |
rs779805542 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51044351 | CCTAACCCATCCCTA[G/T]ATTATTCCAAGCAGC | 114088 |
rs779819385 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50982848 | TATAAATATCACACT[C/T]GAGAGATGTAATTGC | 114088 |
rs779853006 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014999 | GGACAGTGAATTAAT[C/G]TGCAGTCCACAGTTT | 114088 |
rs779864461 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51043307 | ATGGCCTTGAGAGCA[C/G]AAGGCAGCTGAGACA | 114088 |
rs779877956 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078818 | ACAGGCCTGGAGATC[A/G]AATGTATAACATGAG | 114088 |
rs779881777 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066450 | CTAGGTTCTGGAACA[C/T]CACATTCCTGATTTT | 114088 |
rs779890305 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51022747 | CCTCTCCTCCTGTCC[A/G]TGGGAAGGAATTCTC | 114088 |
rs779905287 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51026324 | TGATGGCATCTTTGA[G/T]CAGCTGAGTCAACAC | 114088 |
rs779937272 | snp | C/G | 0.00199892 | 0.0315518 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50981908 | TTCATCACGTCCATG[C/G]GAGCCACACCAAAGG | 114088 |
rs779942357 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009427 | AAGCAAATCTGAACA[C/T]TTTTGTGAGTTGGGG | 114088 |
rs779945350 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51011761 | AATACTCTTATCATT[C/G]TAGTGTAAATTTTTA | 114088 |
rs779989739 | snp | C/T | 3.32303e-05 | 0.00407603 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094128 | CTCACCTTATGTAGT[C/T]TCCACATGGCCCCCA | 114088 |
rs779998471 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51014432 | CTCTCGCTACAGTTG[A/G]TTTTGGTCCACCTTT | 114088 |
rs780002091 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51067202 | TTCTTCATCTTAATA[C/T]ATAGTGCCATTATTT | 114088 |
rs780010609 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005097 | TGGAAAGCTATTACC[A/G]GTACACTGTTAAAGA | 114088 |
rs780051939 | snp | C/G | | | utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095514 | CCAGCGTTTGCGTTT[C/G]GCTCCCAGCTCTGAG | 114088 |
rs780053286 | snp | G/T | 0.000155364 | 0.00881237 | intron-variant, missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50985985 | GACTGTAAAGAGGAA[G/T]GCAAGCTCAGCTGGT | 114088 |
rs780082786 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51084427 | TGGCAGAAGGTAGCC[A/G]GATGACACAAGGTAG | 114088 |
rs780123736 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992782 | CAGCGTGATGCTGAG[A/C]GTCTAATCGGGGAGA | 114088 |
rs780178877 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994847 | TTATTTGAAAATTTC[A/G]TTAAAATTCTTAATT | 114088 |
rs780187689 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51065410 | GATGGATAATGGATG[C/T]TTAAGAGAGTCCAGG | 114088 |
rs780205890 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51079510 | TTTCAAAAGAAAAGA[-/T]TATTATGTGAGTGCA | 114088 |
rs780295564 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047704 | ACAATCTGTATCAGG[C/T]AAAAAAGAATATGGC | 114088 |
rs780336697 | snp | G/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022892 | CTGGGCTTTTCTTCT[G/T]TTGAGGGCATCGATG | 114088 |
rs780349322 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51070018 | CATAGCTGAGGTTGA[G/T]CAGGGTAATGCTCCT | 114088 |
rs780393424 | snp | A/G | | | stop-gained, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094189 | CCTCCTCCAAGCACT[A/G]GTAGCACACGGGCAT | 114088 |
rs780411462 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51041787 | GTTTTAAAAAATTTT[A/G]AAGCCTAATATGATG | 114088 |
rs780446806 | snp | C/G | 3.73713e-05 | 0.00432253 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094607 | GGCCGGTGACAAGTG[C/G]GTGGCCGGTGGCGGC | 114088 |
rs780451421 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071797 | GGTGACAGAGTGAGC[C/T]CTGTCTCAAAAAATA | 114088 |
rs780479451 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50998371 | CTAATCTGTAAAATG[A/G]GATAATAATATCCAC | 114088 |
rs780510159 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51060746 | TGCTGGGATTGCAGG[C/T]GTGAGCCTCTGCACC | 114088 |
rs780533865 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019048 | CATATGTAAAGTTTC[C/T]GAAGAAAGCATAGAT | 114088 |
rs780544989 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058323 | AGGCTCACATCTACA[G/T]AATGGAAAAGGTATT | 114088 |
rs780573031 | snp | C/G | 0.000120446 | 0.0077594 | intron-variant | TRIM9 | GRCh38.p7 | 14:50982929 | TTGGTAACAGAATAA[C/G]GTTATTCCATACCTG | 114088 |
rs780599802 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50979876 | AACTCATTCATTAGG[G/T]TCTCTACCACTGAGT | 114088 |
rs780619120 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50990353 | CATTAGCCAACGCTA[C/T]TGAACACCTGTCATG | 114088 |
rs780622170 | snp | A/C | 3.34638e-05 | 0.00409033 | intron-variant | TRIM9 | GRCh38.p7 | 14:51009029 | TCCTGCTTCAAGCAC[A/C]AGCATCCACTCAGGA | 114088 |
rs780630344 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50983512 | AGCACCAGTTGAATA[C/T]AGATACCAGAGGCCT | 114088 |
rs780632771 | in-del | -/ATT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040856 | ACTACCACTGCTTCA[-/ATT]ATTCTGAAAATAAAA | 114088 |
rs780662373 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019473 | TTTTTGCTTTTTTTT[A/T]GCTCATCAAACTTTG | 114088 |
rs780665479 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047049 | GATGGGGACGGGGAT[A/T]CATGGAGTGTCATTT | 114088 |
rs780667250 | snp | A/G | 4.94214e-05 | 0.00497074 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979393 | GGTGCTTACCTGCAC[A/G]TTCCTGTTCAGGCTG | 114088 |
rs780667495 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51058969 | GGAAAGAAGGGTTGC[A/G]GAATCTTGGGCTGAC | 114088 |
rs780678521 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50991936 | GCTGCTCCTTTGTAA[C/T]CTAGAAATATACAAA | 114088 |
rs780730551 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51091770 | AAAGATCAGAGAATA[A/G]ATGGTCTTCTAGCCT | 114088 |
rs780737903 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995066 | TATGTTGCCCAGGCA[A/G]GATTCAAACTCCTGG | 114088 |
rs780746487 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50979468 | ACCTTGTTGTTCATC[A/G]TTGATAAAAAATGTC | 114088 |
rs780748603 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51028031 | TCTGTATAAGACAGA[A/C]TTGATACCCATAGAT | 114088 |
rs780773355 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040744 | TGAGAAGCGTGTGAA[C/T]CTTTCATATTAATGA | 114088 |
rs780811125 | in-del | -/TTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013227 | AAGTGTCTAACTTCA[-/TTT]TTTTTTTTTTTTTGC | 114088 |
rs780819381 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045550 | TGGAAGGTCCCTTCC[A/G]ACTGGATGTCCTATG | 114088 |
rs780824551 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092667 | TTTAAAAAATGAAAA[G/T]CAAATTCATGCACAT | 114088 |
rs780841065 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51023721 | GTTATTAAGGATAAG[C/T]TTTTCAATGAGTAAT | 114088 |
rs780847655 | snp | A/G | 1.64982e-05 | 0.00287208 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094152 | GCCCCCAGAGCCTTG[A/G]CTTCGTGGCTGGAGT | 114088 |
rs780907368 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046065 | AGCAAATTGCAATAC[A/G]ATAGAGAGGTAAAAA | 114088 |
rs780929957 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080854 | TGCTATATCCAGGGA[C/T]CCTGATAAAGAAATG | 114088 |
rs780944125 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034081 | ACTGGTAATCCATGA[C/G]TTTTCAAACTGGTAA | 114088 |
rs780944416 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51000985 | CAGGATCCTTCACAG[A/T]GTCCCCAGGAGTCAG | 114088 |
rs780983571 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51005714 | ATATGTTGTTTTCTA[C/T]AAAAGAAAAGTCTGA | 114088 |
rs781011772 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032915 | TGAGCGTCTTGTCAG[C/T]ACTCAGAAAGTTTTG | 114088 |
rs781015121 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51022909 | TGAGGGCATCGATGA[A/G]GGCATCACATTGGGC | 114088 |
rs781035328 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51013506 | GATTGTTTATTTACA[C/T]CGCCCAATTTTCTGA | 114088 |
rs781070176 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089602 | AGAATCTGAAAAAAA[C/T]GGAGCCTTATCAGCT | 114088 |
rs781073146 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51017150 | GTTCACTAAAACTTA[C/T]AGCATTTAACTTAAA | 114088 |
rs781074826 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50999572 | GTACTTAAACCTAGT[G/T]GGGGATCAAAAACAC | 114088 |
rs781076010 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995727 | AAAGATTTTGTTACA[A/C]TAGAAAGCCAGAACG | 114088 |
rs781088488 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993110 | TTTGGTAGTATCAGA[G/T]CCTCAGAGATGTAGC | 114088 |
rs781096924 | snp | C/T | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50978498 | ACTGTGCACAGGCTG[C/T]TCCCTCTGTCTGGAA | 114088 |
rs781143623 | in-del | -/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50995106 | ATCCTCCCGTCTCAA[-/C]CTCCCAAGTATCTGG | 114088 |
rs781162206 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50994642 | CCCTGTATGATTTTT[C/T]AAAACAGGAGTACAG | 114088 |
rs781180777 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055471 | GCTAACCAGTAAACA[C/T]AGAGACTATCAAAAT | 114088 |
rs781181569 | snp | C/T | 1.95158e-05 | 0.0031237 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094794 | CCCGCGGCCCGATGG[C/T]TCTGGGGGGATTCAG | 114088 |
rs781199778 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078685 | TAAAGTATTACTTAC[A/G]TGGAATCTAAAAAAG | 114088 |
rs781220813 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51048243 | CTCTGCCTTGTGAAT[A/G]TCTATCTGTACAGGC | 114088 |
rs781229456 | snp | A/C | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51066684 | GAGCACATTCAAAGC[A/C]CTCCAGTCTGCTGCG | 114088 |
rs781241096 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51035103 | ATTTTGTTGACATAT[A/G]GAGACATGCATTATC | 114088 |
rs781272629 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51010991 | CCCCTCCCCACAGCC[C/G]CACGGTCAATTGTTC | 114088 |
rs781273932 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50987069 | TGGATCTTTCGCCAA[C/T]TGAAGCCTTCTTAAC | 114088 |
rs781302578 | snp | A/G | 9.94299e-05 | 0.00705018 | intron-variant | TRIM9 | GRCh38.p7 | 14:51010362 | CATTTAGAATCTGAC[A/G]CAGAAACTAGTTAAC | 114088 |
rs781305014 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51073693 | GAGGCTGATGATATC[C/G]TGATATTCTGTTCTT | 114088 |
rs781312974 | in-del | -/C | | | intron-variant, utr-variant-3-prime | TRIM9 | GRCh38.p7 | 14:50979201 | AGTATAAAGAAGGTG[-/C]CTTATGCTTGGCGTG | 114088 |
rs781324608 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51055061 | GATCTTGACCTCGTG[A/T]TCCGTCCGCCTCGGC | 114088 |
rs781332184 | snp | C/T | 7.53878e-05 | 0.00613907 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51094622 | GGTGGCCGGTGGCGG[C/T]ATAGCCGGGGGAAAC | 114088 |
rs781365920 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980732 | TGCCGATCACTGAAG[A/G]TAACCACTTATCTAC | 114088 |
rs781381507 | snp | A/C | 1.64879e-05 | 0.00287118 | missense, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51009209 | CCTCAGTCAGGTGCA[A/C]TCTTCTTATGAGGGC | 114088 |
rs781381813 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037192 | TAAGAAGCGCCATTC[-/T]AAATAACTCCGAGAT | 114088 |
rs781436299 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51038008 | GCATGTGAATTCTGC[C/T]TCTTGATGCCGTAGG | 114088 |
rs781451071 | snp | A/G | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51097230 | GAAGTCGCTTGAGAT[A/G]ATTTCATTGTTAGAT | 114088 |
rs781466389 | snp | A/G | 0.000123236 | 0.00784875 | intron-variant, synonymous-codon, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50986052 | GGAAGCTGGGTTGTA[A/G]ATTAAGGGTGGAGGA | 114088 |
rs781474470 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059232 | CCAAACAGCACTTCA[A/G]TAACTTTCCCTCATG | 114088 |
rs781511407 | snp | C/T | 0.000108822 | 0.00737557 | utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:50977244 | CCTTGCTGTGGCTCT[C/T]GCAGGCGGAGGTAAG | 114088 |
rs781543140 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51019583 | TATGAGCTAATTCTA[A/G]GCTATGAATTATGGT | 114088 |
rs781588279 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51074198 | CTGAGACAGGAGGAT[C/G]ACTTGAGCCCAGGAG | 114088 |
rs781618080 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027670 | ATGATTGGGTCTCAG[C/G]TACAATATTATTTGG | 114088 |
rs781673073 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51047758 | GCTATGGGCAATGCA[C/T]CTTAGAAAACAAGAA | 114088 |
rs781695521 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51009760 | TTCTTATATTCAATC[A/G]CTTTCTGTCACTCTT | 114088 |
rs781701417 | snp | A/G | 4.04375e-05 | 0.00449635 | intron-variant, missense | TRIM9 | GRCh38.p7 | 14:50998013 | CTTTAGATGCCACGC[A/G]GTTCTCGCTCTGAGG | 114088 |
rs781739906 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51089670 | TTAATATATAAATCT[C/T]TGTATAGTATTCTTA | 114088 |
rs781750755 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51037086 | ACCAAGATTTGTCCA[C/T]GATTAAGTCAAAATT | 114088 |
rs796097229 | in-del | C/TTT | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50980992 | GTATTTTTTTTTTTT[C/TTT]AGAGACACTAATGAG | 114088 |
rs796106330 | snp | C/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51027477 | GTTTTCTTCATTCTT[C/G]CTCACACAAACACCT | 114088 |
rs796206158 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51046127 | TGGAGGACAGTTTAG[C/T]AGTAGCCAGGGATTA | 114088 |
rs796238984 | snp | G/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51032948 | TTTTGGAGCACTTCA[G/T]ATTTCAGATTTTTGG | 114088 |
rs796245459 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51021992 | CAATTCAAAAACACA[-/T]TTTTTTTGCCTGTGT | 114088 |
rs796245999 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51071372 | CAAGAGTGAAACTCC[A/G]TCTAAAAAAAAAAAG | 114088 |
rs796253432 | snp | A/T | | | upstream-variant-2KB, intron-variant | TRIM9 | GRCh38.p7 | 14:51096532 | GCAGCTATGTTGATA[A/T]TTTAAAAGTACTTTA | 114088 |
rs796276184 | in-del | AA/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50992417 | CCCTGTCTCTACGGA[AA/G]AAAAAAAAAGCCAGG | 114088 |
rs796355497 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51050514 | AAATTACCCAGTCTT[A/G]TGTATGTCTTTATCA | 114088 |
rs796408135 | in-del | -/AA | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51088989 | CAAGCTAAAGCAAAG[-/AA]AAAAAAAAAAAGACT | 114088 |
rs796505484 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | TRIM9 | GRCh38.p7 | 14:51095874 | ATCTATGACCCCTTC[A/G]TTTCATGCTTTAAAT | 114088 |
rs796531542 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51092799 | GCAATAGATAAATAC[-/A]AAAAAATAACATAAT | 114088 |
rs796545229 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51040259 | AATTGACCAACAGAA[A/G]TAGTTGACTGAATTT | 114088 |
rs796550693 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51059798 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAACAA | 114088 |
rs796554880 | in-del | -/AGG | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51034696 | AAACTATTCTAAAAT[-/AGG]AGATTAATTAAATAA | 114088 |
rs796575293 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51045057 | CATGTGAAAATATGG[-/A]AAAAAAAAATCAAAT | 114088 |
rs796600313 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51078944 | ATGATAGACATGTTA[A/G]TCTGCTTTACTATAG | 114088 |
rs796631574 | snp | C/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053523 | TCTTTTTTTTTTTTT[C/T]TTTTTTATGCGTTAA | 114088 |
rs796867938 | snp | A/G | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51054809 | CTCCCAAAGTGCTGC[A/G]ATTACAGGCGTGAGC | 114088 |
rs796887266 | in-del | -/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:50993372 | TTTTCAACAAGACTC[-/T]TTTTTTTTTTTTTGA | 114088 |
rs796927498 | snp | A/T | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51053553 | ACATTACATTTATTT[A/T]TTTATTTTTTTTTAC | 114088 |
rs797002357 | in-del | -/A | | | intron-variant | TRIM9 | GRCh38.p7 | 14:51080536 | CTTAATGTAAATAAT[-/A]AAAAAAAAGGGGTCT | 114088 |