SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4386 | snp | C/T | 0.440057 | 0.162414 | intron-variant | TOM1 | GRCh38.p7 | 22:35345178 | CTGGCCTTGTCTGGT[C/T]AACTTCGCGCCTCTG | 10043 |
rs4461 | snp | C/T | 0.497776 | 0.0332724 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299809 | GCGGGGCGGTGGCAC[C/T]GCGAAGCTCGACCAC | 10043 |
rs4462 | snp | A/G | 0.498652 | 0.0259235 | intron-variant | TOM1 | GRCh38.p7 | 22:35301399 | ATCGCTTGGCAGTAG[A/G]TCTCATAGGTGCTCA | 10043 |
rs4463 | in-del | -/A | 0.498673 | 0.0257246 | intron-variant | TOM1 | GRCh38.p7 | 22:35301811 | GGTGGGTGTGTGTCC[-/A]GGGGAGGGCAGGGGT | 10043 |
rs4464 | snp | A/G | 0.457853 | 0.138915 | intron-variant | TOM1 | GRCh38.p7 | 22:35304624 | GCTGGGACTACAGGC[A/G]CCCGCCACCACACCT | 10043 |
rs4465 | snp | C/T | 0.497613 | 0.0344622 | intron-variant | TOM1 | GRCh38.p7 | 22:35312797 | AGGAAGGGGGTACAG[C/T]TGACTGTGGCTGACG | 10043 |
rs4466 | snp | A/G | 0.229723 | 0.249176 | intron-variant | TOM1 | GRCh38.p7 | 22:35327838 | ATGCGCCAGCCACTG[A/G]TCTTGGGGAGCCAAG | 10043 |
rs4467 | snp | C/T | 0.219049 | 0.248077 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335252 | CTAGATTATGGGATC[C/T]TCCCACTGACCCCAC | 10043 |
rs4509 | snp | C/T | 0.498459 | 0.0277128 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298216 | ACCCAGTAACTAGCA[C/T]ATGAAAGCTTAAATA | 10043 |
rs4510 | snp | A/G | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35303460 | TGAGTGTATGGAAAC[A/G]TTAGCTCTTCCTGTC | 10043 |
rs4511 | snp | C/G | 0.480223 | 0.0974544 | intron-variant | TOM1 | GRCh38.p7 | 22:35320601 | CCCCACTCCCCCCAG[C/G]TGGTCCTTCCCATCT | 10043 |
rs6480 | in-del | -/CA | 0.499087 | 0.0213463 | intron-variant | TOM1 | GRCh38.p7 | 22:35314217 | GGAGGCTGTGGGACA[-/CA]TCTGCCCAGACCATC | 10043 |
rs6481 | in-del | -/GTGGA | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35305907 | GTGTTGGTTAGCAGA[-/GTGGA]CTAGACCAGGGTCAG | 10043 |
rs25015 | snp | C/T | 0.453697 | 0.14494 | intron-variant, downstream-variant-500B | TOM1, MIR6069 | GRCh38.p7 | 22:35336610 | GGGGTGTCCTTCCCC[C/T]GCTTTGTCCGCATCT | 10043 |
rs129433 | snp | C/T | 0.49121 | 0.0657086 | intron-variant | TOM1 | GRCh38.p7 | 22:35346531 | TGTCAGCCTTTCCCC[C/T]CCAGGGGTGAGGACC | 10043 |
rs133395 | snp | A/C | 0.34146 | 0.23267 | intron-variant | TOM1 | GRCh38.p7 | 22:35343934 | cacacacatctacac[A/C]caccacctacacaca | 10043 |
rs133396 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | TOM1 | GRCh38.p7 | 22:35344281 | CCAGGCCCGGCCACC[C/T]GGAAAGCTGGGGGTG | 10043 |
rs133397 | snp | A/C | 0.32627 | 0.238082 | intron-variant | TOM1 | GRCh38.p7 | 22:35344449 | GTTGGCCCGGCCAGC[A/C]CAGCTTCCGCAGCTC | 10043 |
rs133398 | snp | A/G | 0.298638 | 0.245223 | intron-variant | TOM1 | GRCh38.p7 | 22:35345827 | ACAGCAGGAGGACCC[A/G]TTGTTCTCACCAAGA | 10043 |
rs133399 | snp | A/G | 0.428937 | 0.17459 | intron-variant | TOM1 | GRCh38.p7 | 22:35345870 | GGCCAGGGTAGACTT[A/G]TATAGCATATAGCAC | 10043 |
rs133400 | snp | A/G | 0.316726 | 0.240931 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348479 | AGGACTCCATGAGCC[A/G]CCCAGCTCAGAGGAG | 10043 |
rs138719 | in-del | -/AAAT | 0.497586 | 0.0346604 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297380 | AGACTCTGTCTTTAA[-/AAAT]AAATAAATAAATAAA | 10043 |
rs138721 | snp | C/G | 0.492337 | 0.0614248 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297751 | CTGGGCACGGTGGCT[C/G]ACACCTGTAATCACA | 10043 |
rs138722 | snp | A/G | 0.498437 | 0.0279115 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297785 | CAAACAGGAAGTGGA[A/G]TCATAAACTCCATGC | 10043 |
rs138723 | snp | G/T | 0.495927 | 0.0449436 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297837 | TTTTTGTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 10043 |
rs138725 | snp | G/T | 0.0803491 | 0.183626 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297853 | TTTTTTTTTTTTTTT[G/T]TTTTTACCATGAATA | 10043 |
rs138726 | snp | A/G | 0.498437 | 0.0279115 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298302 | GACTCGTGGGGGCAA[A/G]GGCATTTGTGAACAG | 10043 |
rs138727 | snp | A/C | 0.495368 | 0.0478996 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298900 | AGAAAAGGTCATAAC[A/C]CATAGATAGGTATCT | 10043 |
rs138728 | snp | C/G | 0.581451 | 0.106738 | intron-variant | TOM1 | GRCh38.p7 | 22:35300084 | CTACACGCCAGCCTC[C/G]TTGCCCTCCCTGCCT | 10043 |
rs138729 | in-del | -/C | 0.498632 | 0.0261223 | intron-variant | TOM1 | GRCh38.p7 | 22:35300906 | CCATATAAAAAAAAA[-/C]AGTTGTAATATTTAT | 10043 |
rs138730 | snp | A/G | 0.483636 | 0.0889627 | intron-variant | TOM1 | GRCh38.p7 | 22:35300938 | ATCACTGGGCTGGGC[A/G]CGGTGGCTCCCGCCT | 10043 |
rs138732 | in-del | -/TATAT | 0.498908 | 0.0233371 | intron-variant | TOM1 | GRCh38.p7 | 22:35301315 | ACATACACATACATA[-/TATAT]TATATGTATTTACAC | 10043 |
rs138733 | snp | C/G | 0.494315 | 0.0530107 | intron-variant | TOM1 | GRCh38.p7 | 22:35301619 | AGGTTTCGCAAGACA[C/G]TAAGAATGGAAAATA | 10043 |
rs138734 | in-del | -/TTT | | | intron-variant | TOM1 | GRCh38.p7 | 22:35302350 | TTTTTTTTTTTTTTT[-/TTT]GAGACTGCGTTTCGC | 10043 |
rs138735 | snp | G/T | 0.498652 | 0.0259235 | intron-variant | TOM1 | GRCh38.p7 | 22:35302358 | TTTTTTTTTTGAGAC[G/T]GCGTTTCGCTCTTGT | 10043 |
rs138736 | snp | A/G | 0.495782 | 0.0457324 | intron-variant | TOM1 | GRCh38.p7 | 22:35302422 | CTCACTGCAACTTCC[A/G]CCTCCCGGGTTCAAG | 10043 |
rs138737 | in-del | -/G | 0.492727 | 0.0598633 | intron-variant | TOM1 | GRCh38.p7 | 22:35302463 | GCCTCAGCCTCCCAA[-/G]GTAGCCGGGATTACA | 10043 |
rs138738 | snp | A/G | 0.498652 | 0.0259235 | intron-variant | TOM1 | GRCh38.p7 | 22:35302498 | CGCTCCGCCACACCC[A/G]ACTAATTTTGTATTT | 10043 |
rs138739 | in-del | -/ACACACACAC | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35303149 | CACACACACACACAC[-/ACACACACAC]CCCTTTGTGCTTGCT | 10043 |
rs138740 | snp | C/T | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35303589 | tgcaacctctgcccc[C/T]caggttcaagtgatt | 10043 |
rs138741 | snp | C/T | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35303670 | tctctactaaaaata[C/T]aaaaattagccgggc | 10043 |
rs138742 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | TOM1 | GRCh38.p7 | 22:35303766 | tcacacctgcaatcc[C/T]agcactttgggaggc | 10043 |
rs138743 | snp | C/T | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35303772 | ggtggctcacacctg[C/T]aatcccagcactttg | 10043 |
rs138744 | snp | C/T | 0.498652 | 0.0259235 | intron-variant | TOM1 | GRCh38.p7 | 22:35303890 | ACAGCTAGGCTGAAC[C/T]TCTTGAGAGCAGGAA | 10043 |
rs138745 | snp | A/G | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35304262 | AGAGCCACAACTCTT[A/G]TTCTACCCTCAGATA | 10043 |
rs138746 | snp | A/G | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35304474 | TACTGGATCTGTTTT[A/G]TTTTTTGTTTTTTGT | 10043 |
rs138747 | snp | A/T | 0.501825 | 0.040059 | intron-variant | TOM1 | GRCh38.p7 | 22:35304495 | TGTTTTTTGTTTTTT[A/T]TGAGACAGAGTCTCA | 10043 |
rs138748 | snp | G/T | 0.498754 | 0.0249289 | intron-variant | TOM1 | GRCh38.p7 | 22:35304526 | CTCTGTCGCCCAGGC[G/T]GGAGTGCAGTGGCGC | 10043 |
rs138749 | snp | A/G | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35304770 | GGCGTGAGCCACTGC[A/G]CCCGGCCTACTGGCT | 10043 |
rs138750 | snp | C/T | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35304774 | ACAGAGCCAGTAGGC[C/T]GGGTGCAGTGGCTCA | 10043 |
rs138751 | snp | A/T | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35304811 | GAAATGGAAAATGGG[A/T]TTCTTGATATCTGTC | 10043 |
rs138752 | snp | C/T | 0.498794 | 0.0245311 | intron-variant | TOM1 | GRCh38.p7 | 22:35305230 | GCAATGGAGAGGGAC[C/T]GTGACATAGTTAGGA | 10043 |
rs138753 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | TOM1 | GRCh38.p7 | 22:35305433 | acctcgtgatccacc[C/T]gcctcggcctcccaa | 10043 |
rs138754 | snp | C/T | 0.0879971 | 0.190408 | intron-variant | TOM1 | GRCh38.p7 | 22:35305457 | acgaggtcaagaaat[C/T]gagaccatcctggcc | 10043 |
rs138755 | snp | A/G | 0.498794 | 0.0245311 | intron-variant | TOM1 | GRCh38.p7 | 22:35305580 | caggaaaattacttg[A/G]acctgggaggcgaag | 10043 |
rs138756 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | TOM1 | GRCh38.p7 | 22:35305616 | agtgagccaagatca[C/T]gccgctgcactctag | 10043 |
rs138758 | snp | A/C | 0.498754 | 0.0249289 | intron-variant | TOM1 | GRCh38.p7 | 22:35305729 | ctgtaaccacacacc[A/C]tgcccttggagccct | 10043 |
rs138759 | snp | C/T | 0.498754 | 0.0249289 | intron-variant | TOM1 | GRCh38.p7 | 22:35305730 | cctgtaaccacacac[C/T]atgcccttggagccc | 10043 |
rs138760 | snp | A/C | 0.456685 | 0.140646 | intron-variant | TOM1 | GRCh38.p7 | 22:35306075 | tgtgcataaataaaa[A/C]tatttatgggcaatg | 10043 |
rs138761 | in-del | -/T | 0.498009 | 0.0314867 | intron-variant | TOM1 | GRCh38.p7 | 22:35306145 | TTATTCTTCTTCAGC[-/T]TTTTTTTTTCCCAAC | 10043 |
rs138762 | snp | A/T | 0.498774 | 0.02473 | intron-variant | TOM1 | GRCh38.p7 | 22:35306181 | aaaaatataaagacc[A/T]tctgtagctcgagta | 10043 |
rs138763 | in-del | -/C | 0.497722 | 0.0336691 | intron-variant | TOM1 | GRCh38.p7 | 22:35306748 | TTATCATTCCTGGGA[-/C]CCCAGTCTAAGTTAG | 10043 |
rs138764 | snp | C/T | 0.497445 | 0.0356514 | intron-variant | TOM1 | GRCh38.p7 | 22:35307135 | TCTTTACTGCCTTAC[C/T]AAGGAGATCTTGATC | 10043 |
rs138765 | snp | C/T | 0.498158 | 0.0302955 | intron-variant | TOM1 | GRCh38.p7 | 22:35307288 | TCATGGATATAATTA[C/T]ATAGGATGAGGTCAA | 10043 |
rs138766 | snp | A/C | 0.497151 | 0.037632 | intron-variant | TOM1 | GRCh38.p7 | 22:35307329 | ATGCAGGATAGGAAA[A/C]AAACACGAACATCAA | 10043 |
rs138767 | snp | C/T | 0.498133 | 0.030494 | intron-variant | TOM1 | GRCh38.p7 | 22:35307373 | GCAGGAGAGGAAAAA[C/T]TTAATGTCCCTCTAA | 10043 |
rs138768 | snp | A/T | 0.161924 | 0.233971 | intron-variant | TOM1 | GRCh38.p7 | 22:35307558 | GTCCCCCAGGTCTCC[A/T]CCTCAAGGGACACGG | 10043 |
rs138769 | snp | C/G | 0.498277 | 0.0293024 | intron-variant | TOM1 | GRCh38.p7 | 22:35308228 | CCTGTGTGTGTGTGT[C/G]TGtctgtctctctct | 10043 |
rs138770 | in-del | -/T | 0.499325 | 0.0183582 | intron-variant | TOM1 | GRCh38.p7 | 22:35308276 | CTAGTTCCTTTTCTC[-/T]TTTTTTTTTTTTTTC | 10043 |
rs138771 | snp | A/G | 0.478685 | 0.10101 | intron-variant | TOM1 | GRCh38.p7 | 22:35309366 | GAACTGAAAGAGGCC[A/G]GGCGCAGTGGCTCAC | 10043 |
rs138772 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35309660 | AAAAAAAAAAAAAAA[-/A]GAGAGAGAACTGAGA | 10043 |
rs138773 | snp | C/G | 0.495291 | 0.0482933 | intron-variant | TOM1 | GRCh38.p7 | 22:35309949 | TTTAGCTTTTCTAGA[C/G]CCCCTTGCAGCCAGA | 10043 |
rs138774 | snp | A/G | 0.495782 | 0.0457324 | intron-variant | TOM1 | GRCh38.p7 | 22:35312806 | GTACAGCTGACTGTG[A/G]CTGACGCCAGCCCCT | 10043 |
rs138775 | snp | A/G | 0.495782 | 0.0457324 | intron-variant | TOM1 | GRCh38.p7 | 22:35313072 | TGGCCGGACACAGTG[A/G]GCAGTGGCTCACACC | 10043 |
rs138776 | in-del | -/TG | | | intron-variant | TOM1 | GRCh38.p7 | 22:35314218 | ATGGTCTGGGCAGAT[-/TG]GTCCCACAGCCTCCC | 10043 |
rs138777 | snp | C/T | 0.498632 | 0.0261223 | intron-variant | TOM1 | GRCh38.p7 | 22:35315105 | CCATTCTCCACACTG[C/T]CCAGAAGGAACTTTC | 10043 |
rs138778 | snp | C/T | 0.496348 | 0.0425753 | intron-variant | TOM1 | GRCh38.p7 | 22:35316139 | CAGGTGTGCCAAGGC[C/T]GGCAGGGTGGCTGCA | 10043 |
rs138779 | snp | C/T | 0.495963 | 0.0447464 | intron-variant | TOM1 | GRCh38.p7 | 22:35316184 | ACTTTGCATGTGACA[C/T]TTGCAGGGGAGGGAA | 10043 |
rs138780 | snp | C/T | 0.477345 | 0.103991 | intron-variant | TOM1 | GRCh38.p7 | 22:35316560 | GGCTGCAGGTCTGCA[C/T]GGTAGCAAGCACCGG | 10043 |
rs138781 | snp | C/T | 0.497091 | 0.0380279 | intron-variant | TOM1 | GRCh38.p7 | 22:35316621 | CCAGAACTCTGCAGC[C/T]GACTCCCGGCCTGGA | 10043 |
rs138782 | snp | A/C | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35320138 | CACCATCCCTGCCCT[A/C]TAGCAAGCTTCTTCT | 10043 |
rs138783 | in-del | -/A/AAAAAAAAAAAAAA/GAAAAAAAAAAAAA | 0.224412 | 0.248687 | intron-variant | TOM1 | GRCh38.p7 | 22:35320987 | GAAAAAAAAAAAAAA[lengthTooLong]CTTGAATGGAAGGGT | 10043 |
rs138784 | snp | A/G | 0.475789 | 0.107327 | intron-variant | TOM1 | GRCh38.p7 | 22:35321253 | TTCTCATGCTCCCCA[A/G]GGGTTTCTTATGCAT | 10043 |
rs138785 | snp | G/T | 0.494484 | 0.0522255 | intron-variant | TOM1 | GRCh38.p7 | 22:35328666 | TTAGCACGGGGACAG[G/T]GCGGGTGCCTTTCAA | 10043 |
rs138786 | snp | C/T | 0.49168 | 0.063958 | intron-variant | TOM1 | GRCh38.p7 | 22:35332473 | GACAAGGCCACGACT[C/T]GAACAGACCCCACAC | 10043 |
rs138787 | snp | C/T | 0.235564 | 0.249583 | intron-variant | TOM1 | GRCh38.p7 | 22:35332607 | ACACACACACACACA[C/T]ACACACACACAAATA | 10043 |
rs138788 | snp | A/G | 0.488965 | 0.0734569 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35333728 | AATCCTACCATCCTA[A/G]GATTGGCCCTCTACA | 10043 |
rs138789 | snp | A/C | 0.454544 | 0.143743 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334092 | ATGGATAGCGTTTTG[A/C]CTGTTCTCTAACGCT | 10043 |
rs138790 | snp | A/G | 0.487241 | 0.0788465 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35336911 | GTGGGCAGGGGTGGC[A/G]AGGAGCTAAGCTTAG | 10043 |
rs138791 | in-del | -/T | 0.418007 | 0.185132 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35336943 | TTTTTTTTTTTTTTT[-/T]GAGCCGGAGTCTCGC | 10043 |
rs138792 | snp | A/G | 0.493568 | 0.0563433 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337000 | GGCTGGAGTGCAGTG[A/G]CGCTTGCAGAGTGCA | 10043 |
rs138793 | snp | C/G | 0.491577 | 0.0643472 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337343 | TAGAGACAGCAACAA[C/G]CACCTCCAGACCCTC | 10043 |
rs138794 | snp | C/T | 0.488485 | 0.0749998 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337661 | CACATTTAACTCTTG[C/T]AATACCAGCTTGCTT | 10043 |
rs138795 | snp | A/G | 0.493107 | 0.0583 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337715 | ACGCTAGTGAAGCGG[A/G]GCTGGTCTAACTGTA | 10043 |
rs377904 | snp | G/T | 0.498652 | 0.0259235 | intron-variant | TOM1 | GRCh38.p7 | 22:35303052 | ATTAGAATCACCATC[G/T]GAGGGATGTCAATTC | 10043 |
rs715514 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | TOM1 | GRCh38.p7 | 22:35328822 | CGTGAGGCCACAGTC[A/G]GCAATGCCGGGCAGC | 10043 |
rs739015 | snp | A/G | 0.0663309 | 0.169604 | intron-variant | TOM1 | GRCh38.p7 | 22:35327725 | TCAGGACCCCTTACT[A/G]GGTGCTTTACTCTGT | 10043 |
rs743810 | snp | A/C | 0.408057 | 0.193696 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35346932 | CTCTTCCGCATCATT[A/C]CCCTGGGAAGGTAGA | 10043 |
rs762913 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | TOM1 | GRCh38.p7 | 22:35313772 | ACTGGGCACCTGTGC[A/G]TCCTTACAGCAGTCT | 10043 |
rs762967 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | TOM1 | GRCh38.p7 | 22:35344873 | CACAGCCACCTGGAC[A/G]GTAAGTACTGCTGCT | 10043 |
rs1003676 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TOM1 | GRCh38.p7 | 22:35329734 | TTGCTTAGTCAAAAA[A/G]AAACTGAGTCTGCAA | 10043 |
rs2071745 | snp | C/G | 0.403905 | 0.197049 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347131 | CCCCTCAGCTGAGGG[C/G]CCCCCGGGTCCCCCA | 10043 |
rs2075935 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | TOM1 | GRCh38.p7 | 22:35333614 | TCAGTCTGGACCCCA[C/T]CTTGCTGGGGTCCCA | 10043 |
rs2267329 | snp | A/G | 0.0912534 | 0.193131 | intron-variant | TOM1 | GRCh38.p7 | 22:35308441 | GGCGCGTGCCACCAC[A/G]CCTGGCTAATTTTTA | 10043 |
rs2267330 | snp | C/G | 0.495445 | 0.0475058 | intron-variant | TOM1 | GRCh38.p7 | 22:35308619 | CCTGACTAATACAAA[C/G]CCCACTCCACCCCTG | 10043 |
rs2267331 | snp | C/T | 0.121369 | 0.214369 | intron-variant | TOM1 | GRCh38.p7 | 22:35326133 | TATATGTTCAATGCT[C/T]GGCACTTATTAGGTA | 10043 |
rs2267332 | snp | C/G | 0.121369 | 0.214369 | intron-variant | TOM1 | GRCh38.p7 | 22:35328271 | CTCCGAAAGAGAGAA[C/G]ACTGCGCAGGCAGCC | 10043 |
rs2267334 | snp | C/G | 0.464841 | 0.127841 | intron-variant | TOM1 | GRCh38.p7 | 22:35341221 | TGAGAAAACTGAGTT[C/G]CAGGAAGAGCTTAAG | 10043 |
rs2267335 | snp | A/G | 0.474903 | 0.109173 | intron-variant | TOM1 | GRCh38.p7 | 22:35341468 | TGCAAAGGAGAGTGA[A/G]TGGAGGTGTGTGTCT | 10043 |
rs2267336 | snp | A/G | 0.457154 | 0.139954 | intron-variant | TOM1 | GRCh38.p7 | 22:35344135 | GCACCCCTGTTAGAA[A/G]CCGCGCCCTCCAGTG | 10043 |
rs2283961 | snp | C/T | 0.341685 | 0.232581 | intron-variant | TOM1 | GRCh38.p7 | 22:35342495 | ACCCTACTGGGAGCC[C/T]CCAGACCATCTGACA | 10043 |
rs3177142 | snp | C/T | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323063 | GAACTGCGGGCACCG[C/T]TTCCACGTGCTGGTG | 10043 |
rs3215443 | in-del | -/C | 0.49533 | 0.0480965 | intron-variant, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299681 | ACCGCGCTTCCCGGG[-/C]CCCGACCCCAGACCC | 10043 |
rs3216430 | in-del | -/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305863 | AAGGCAGAAGCCGGG[-/G]TGGGGAGGGCGACTA | 10043 |
rs3219783 | microsatellite | (CA)9/14/15 | 0.564158 | 0.132181 | intron-variant | TOM1 | GRCh38.p7 | 22:35303133 | CACCTCCCCTCCCAA[(CA)9/14/15]CCCTTTGTGCTTGCT | 10043 |
rs3765222 | snp | G/T | 3.2963e-05 | 0.00405961 | intron-variant | TOM1 | GRCh38.p7 | 22:35327238 | GGCCCCAGAACCCTG[G/T]CTTCTCTCACCACGA | 10043 |
rs3788509 | snp | A/G | 0.498323 | 0.0289051 | intron-variant | TOM1 | GRCh38.p7 | 22:35311243 | CCGCGGAGCAGTCCC[A/G]TGGGAAGGCCAGGGC | 10043 |
rs3788510 | snp | C/G | 0.0901694 | 0.192235 | intron-variant | TOM1 | GRCh38.p7 | 22:35319816 | CTCTCAGGCTTCTGG[C/G]CCAGGACCCCCCTTG | 10043 |
rs3788511 | snp | A/G | 0.169435 | 0.236663 | intron-variant | TOM1 | GRCh38.p7 | 22:35319857 | ATCCCTTTCCCCACC[A/G]TGTCCCTTCCACCGC | 10043 |
rs3885458 | snp | C/T | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35328800 | GGCCTCACGCCAGCA[C/T]GCCTTTCTCCTGGAG | 10043 |
rs3885573 | snp | A/C | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35325694 | ACTGAGTTAGACAAT[A/C]ACAAGGTGGTTGTAC | 10043 |
rs4820190 | snp | A/G | 0.346811 | 0.230494 | intron-variant | TOM1 | GRCh38.p7 | 22:35339767 | AAATTAGCCGGGCGT[A/G]GTGGCGGGCGCCTGT | 10043 |
rs5750097 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35325743 | TCTGAAGTCTAGCAT[C/T]TGTGTGGATTAAGAC | 10043 |
rs5750099 | snp | A/G | 0.0869089 | 0.189476 | intron-variant | TOM1 | GRCh38.p7 | 22:35339910 | CTCCGTCTCAAAAAA[A/G]AAAAAAAGAGCGGAC | 10043 |
rs5750100 | snp | G/T | 0.103082 | 0.202275 | intron-variant | TOM1 | GRCh38.p7 | 22:35344650 | GCTCCTGCCTGGGGG[G/T]TCCTCAGGTGCTGGG | 10043 |
rs5755700 | snp | C/G | 0.105924 | 0.204309 | intron-variant | TOM1 | GRCh38.p7 | 22:35340715 | TTGCACTACGACACT[C/G]CAGCCTGGGCAATGG | 10043 |
rs5995087 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35340030 | CCGAGCACATTTTGT[A/G]GGTGACCCCCACACG | 10043 |
rs5995089 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35340601 | aatatttaaaaatta[G/T]ccgggcatggtggcg | 10043 |
rs5999786 | snp | G/T | 0.47802 | 0.102502 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297845 | TTTTTTTGTTTTTTT[G/T]TTTTTTTTTTTTTAC | 10043 |
rs5999794 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35331773 | gtgcctgtaatccca[A/G]cttacttgggaggct | 10043 |
rs5999796 | snp | A/G | 0.448452 | 0.152042 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335101 | GTCTGACCCCTTGCC[A/G]GGACCTGCGGGAGAA | 10043 |
rs5999797 | snp | A/G | 0.0733688 | 0.176922 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335182 | AGCCTTTTGCCCACT[A/G]TGACCCCCAGGGCTG | 10043 |
rs5999798 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | TOM1, MIR6069 | GRCh38.p7 | 22:35336552 | AGCAGGGCTTCTGGG[C/T]GAGCCACAGCAGAGA | 10043 |
rs5999800 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338253 | CTGGTGAGCCAGTGC[A/C]AGACAAGATGGCACC | 10043 |
rs7285466 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35323383 | GGCAGGGCAGATGTA[A/G]TTAAAAAAAAAAAAA | 10043 |
rs7286881 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TOM1 | GRCh38.p7 | 22:35307462 | ATCACTGGGACGTAA[A/G]CAGCCTGAAATGGGG | 10043 |
rs7289046 | snp | C/T | 0.178144 | 0.239451 | intron-variant | TOM1 | GRCh38.p7 | 22:35321547 | GGGATTACAGGGTCA[C/T]ACCACCACGCCCGGC | 10043 |
rs7291620 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334857 | CTCCCTGCACTGTGT[A/G]CCGCATAGTAAGCCC | 10043 |
rs7511276 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35312190 | cggaagttgcagtga[A/G]ccgagatcgcaccac | 10043 |
rs8136021 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TOM1 | GRCh38.p7 | 22:35346110 | AGGCTCTTACCTGCA[A/G]TAGCTCAGAAGACTC | 10043 |
rs8136060 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35346356 | GGCACCAAGGCCCAC[A/T]TGGGCACTTCAGGCC | 10043 |
rs8136135 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35322814 | CCAGCCCACACACCA[C/T]ACCTCTGCCCACCCT | 10043 |
rs8136664 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TOM1 | GRCh38.p7 | 22:35333588 | CCTTGTTATATACCC[A/G]CAGCAGAGTGTCAGT | 10043 |
rs8137168 | snp | A/G | 0.0217236 | 0.101931 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35333660 | CAAGGTGGGGCACTC[A/G]GGGTCACTGCCCCTG | 10043 |
rs8137235 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35326744 | TCCCAGTCCTCTAGG[A/G]GGAGAGAGACGGCGG | 10043 |
rs8137323 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35326589 | AATAGACCAGAAACA[A/G]GACAAAATCCCAGTC | 10043 |
rs8137439 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35326655 | CTAGGAGGAGAGAGA[C/G]GGTGGAATCCCAGTC | 10043 |
rs8137566 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35326743 | ATCCCAGTCCTCTAG[G/T]AGGAGAGAGACGGCG | 10043 |
rs8138139 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35326658 | GGAGGAGAGAGAGGG[C/T]GGAATCCCAGTCCTC | 10043 |
rs8139181 | snp | A/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35322160 | GCTGGAAAGGTCTGT[A/G]GGCAACGCACTGTCC | 10043 |
rs8139565 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35322359 | CGGGGGCAGGGAGGC[C/T]GGCTGACTGAGTTGG | 10043 |
rs8140382 | snp | C/T | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35322308 | GGGCCAAAGGACCTG[C/T]GGGTGACATTGAAGC | 10043 |
rs8140506 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35322382 | TGAGTTGGGTGCTGC[C/T]CGGCACTTTGGTGCT | 10043 |
rs8141467 | snp | A/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35326256 | AGCATTTCTCAAAAC[A/G]TAAAAAGGTTCTTCA | 10043 |
rs8142782 | snp | A/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35322488 | AGGGCGGCCAGACAC[A/G]CGTGGGCCTCCTAGC | 10043 |
rs8142937 | snp | A/T | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35322607 | CAAAAAGCAAAGGCA[A/T]TTCCTGCAGTGGGAA | 10043 |
rs8143056 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | TOM1 | GRCh38.p7 | 22:35344278 | GGGCCAGGCCCGGCC[A/C]CCCGGAAAGCTGGGG | 10043 |
rs9607265 | snp | A/G | 0.0471774 | 0.146161 | intron-variant, nc-transcript-variant | TOM1, MIR3909 | GRCh38.p7 | 22:35335704 | GGGAAAAGCACACAA[A/G]GAACTTGTCCTCTAG | 10043 |
rs9610284 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337507 | CCAGGGAATGCCCCA[C/G]CTAGTGGTCACACTC | 10043 |
rs9619527 | snp | C/T | 0.077417 | 0.180873 | intron-variant | TOM1 | GRCh38.p7 | 22:35319964 | GCTGAGAACCAGTGC[C/T]AGGGTTCCAGGCTCT | 10043 |
rs9622171 | snp | A/G | 0.16028 | 0.233346 | intron-variant | TOM1 | GRCh38.p7 | 22:35305464 | caagaaattgagacc[A/G]tcctggccaacatgg | 10043 |
rs9622172 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35306254 | gctgacttctgAATC[A/G]GAGCAGCTGGCCAGA | 10043 |
rs9622173 | snp | C/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35321013 | aaaaCTTGAATGGAA[C/G]GGTAAATGGACAGAT | 10043 |
rs9622174 | snp | A/G | 0.338069 | 0.233974 | intron-variant | TOM1 | GRCh38.p7 | 22:35329545 | ATCTAAAATTATTCC[A/G]AAGCTAAAAGTTTGT | 10043 |
rs10483190 | snp | A/G | 0.321769 | 0.239477 | intron-variant | TOM1 | GRCh38.p7 | 22:35326018 | TTTTGGAAGGTGTCA[A/G]TGAACCATAGTGGAT | 10043 |
rs11089740 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35344265 | GCATGGTGAGCAGGG[A/G]CCAGGCCCGGCCACC | 10043 |
rs11287122 | in-del | -/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35302331 | TTCTTTTTCTTTTTC[-/T]TTTTTTTTTTTTTTT | 10043 |
rs11558472 | snp | A/G | | | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323075 | CCGCTTCCACGTGCT[A/G]GTGGCCAGCCAGGAC | 10043 |
rs11558473 | snp | A/G | 0.000149277 | 0.00863807 | missense, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323062 | AGAACTGCGGGCACC[A/G]CTTCCACGTGCTGGT | 10043 |
rs11703973 | snp | G/T | 0.172351 | 0.237636 | intron-variant | TOM1 | GRCh38.p7 | 22:35318747 | GAAAACCCAGCGAAG[G/T]CTGGGCAGAGGTGTG | 10043 |
rs11703977 | snp | A/G | 0.170733 | 0.237101 | intron-variant | TOM1 | GRCh38.p7 | 22:35318760 | AGGCTGGGCAGAGGT[A/G]TGGGAGCCGTGGGCA | 10043 |
rs11704012 | snp | G/T | | | intron-variant, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299783 | GACCCTGGCGTCTCA[G/T]GGCGGGGCTTGTGGT | 10043 |
rs11704301 | snp | A/C | 0.182933 | 0.240836 | intron-variant | TOM1 | GRCh38.p7 | 22:35315550 | CTTCACAGGATGGAC[A/C]ACTCTGTCTCTCAGC | 10043 |
rs11705174 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35310020 | GTCAGCTCCACATGG[G/T]AGGGTTAATAAAAAT | 10043 |
rs11705224 | snp | A/G | 0.24019 | 0.249807 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297514 | aggctggagtgcagt[A/G]gtgcaatctctgctc | 10043 |
rs11705397 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35332719 | attcctgtttatttg[G/T]ttcatgctactcatg | 10043 |
rs11705414 | snp | G/T | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297843 | tttttttttgttttt[G/T]ttttttttttttttt | 10043 |
rs11912519 | snp | A/C | 0.0349536 | 0.127495 | intron-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35321842 | CTGGCTGGATACACA[A/C]AACAGGTGGGGCACA | 10043 |
rs11912648 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35315398 | ACTAACCCCCGCCCC[A/C]AAACCCTCCAAAGCA | 10043 |
rs12157479 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304109 | TCACCAAAAGTCAGT[C/G]TAAGAGAAAGCATCG | 10043 |
rs12160421 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338304 | GTGTTTTCAGCAGCA[C/G]AATGGAATCCCCCAT | 10043 |
rs12161017 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35320983 | tgagactctgtctca[C/G]aaggaaaaaaaaaaa | 10043 |
rs12167136 | snp | A/G | 0.00397576 | 0.044408 | intron-variant | TOM1 | GRCh38.p7 | 22:35323961 | CCAGGCAGGTGGGCC[A/G]CACACGTCAGGGAGG | 10043 |
rs12167319 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305083 | CCACAGGAAGGAATC[A/T]CAGAAGTGAGAGACC | 10043 |
rs12168810 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35346416 | CATTTCTGCCCAGGA[C/T]TAAGCCACAGACCAA | 10043 |
rs12170659 | snp | C/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35325977 | GTGTTCATTAAGTAA[C/G]CCAAATAGATCAAAC | 10043 |
rs12171175 | snp | C/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35321043 | TAGAGCAGCTGGCCA[C/G]GACGGGGCATCAGAA | 10043 |
rs12172573 | snp | G/T | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297839 | tttgtttttttttgt[G/T]ttttttttttttttt | 10043 |
rs12484487 | snp | A/G | 0.199564 | 0.24486 | intron-variant | TOM1 | GRCh38.p7 | 22:35328293 | CAGGCAGCCTCGCAC[A/G]CCCCAAGCCAAGGCC | 10043 |
rs12628493 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TOM1 | GRCh38.p7 | 22:35305859 | tgtgaaggcagaagc[C/T]ggggtggggagggcg | 10043 |
rs12628659 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35328965 | Gttttttattttttt[A/T]ttttttttgagacgg | 10043 |
rs12628747 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35328966 | ttttttattttttta[A/T]tttttttgagacgga | 10043 |
rs13054187 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304569 | ctgcaagctccacct[C/T]ccgggttcacgccat | 10043 |
rs13055137 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TOM1 | GRCh38.p7 | 22:35331983 | AAAATGAGGCTTGTG[A/G]CATAAGTGAGAGTCC | 10043 |
rs13056516 | snp | G/T | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297838 | ttttgtttttttttg[G/T]ttttttttttttttt | 10043 |
rs13056521 | snp | G/T | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297851 | tgttttttttttttt[G/T]tttttttACCATGAA | 10043 |
rs13057416 | snp | A/C | 0.0356815 | 0.128715 | intron-variant | TOM1 | GRCh38.p7 | 22:35308087 | tggccagcaggctcc[A/C]cttgtccttgcactt | 10043 |
rs13057766 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343138 | accacacacacacat[C/T]tacacccaccacaca | 10043 |
rs13058668 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | TOM1 | GRCh38.p7 | 22:35321382 | tttttgagacagggt[A/C]tcactctgtcgccca | 10043 |
rs16995569 | snp | C/T | 0.039522 | 0.134904 | intron-variant | TOM1 | GRCh38.p7 | 22:35316498 | TCATCATTCATGTAA[C/T]ACCAATTAGTGCCTC | 10043 |
rs16995578 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | TOM1 | GRCh38.p7 | 22:35319392 | ACCTCACCAAGCATG[A/G]CACCTAAACTTAGCC | 10043 |
rs16995580 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TOM1 | GRCh38.p7 | 22:35325218 | CTGGTGAGTTAGACA[C/T]GGATGTGTGATGGAA | 10043 |
rs16995582 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | TOM1 | GRCh38.p7 | 22:35325761 | TGTGGATTAAGACGC[G/T]AATTACTTCCAATGC | 10043 |
rs16995584 | snp | A/T | 0.128288 | 0.218372 | intron-variant | TOM1 | GRCh38.p7 | 22:35325857 | ACATGTTAAGACATC[A/T]GGTGTGCAGTGATGT | 10043 |
rs28372592 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343115 | ATACACCACACACAC[A/C]CACACACACCACACA | 10043 |
rs28433170 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304480 | ATCTGTTTTGTTTTT[G/T]GTTTTTTGTTTTTTA | 10043 |
rs28434139 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304488 | TGTTTTTTGTTTTTT[G/T]TTTTTTATGAGACAG | 10043 |
rs28491160 | snp | A/C | 0.434543 | 0.168653 | intron-variant | TOM1 | GRCh38.p7 | 22:35343807 | CTACACCTACCCACA[A/C]CTACACCTACACATA | 10043 |
rs28532088 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35319409 | ACCTAAACTTAGCCT[C/T]GTTGCTAAAGTGTCT | 10043 |
rs28571283 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35315488 | CTCTATAAGTGTGGA[A/T]CCCCCAAGGGCAGGG | 10043 |
rs28674998 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35316050 | CAAGTTCTACATGCC[C/T]ACTCTGGCACACACT | 10043 |
rs28682328 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304481 | TCTGTTTTGTTTTTT[G/T]TTTTTTGTTTTTTAT | 10043 |
rs28711188 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304487 | TTGTTTTTTGTTTTT[G/T]GTTTTTTATGAGACA | 10043 |
rs34112350 | in-del | -/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35325128 | CACACTGTGGAGACA[-/C]CCCACGTTAAAGGTG | 10043 |
rs34141195 | in-del | -/A | | | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338296 | TATAGATGTGTTTTC[-/A]AGCAGCAGAATGGAA | 10043 |
rs34280057 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35318947 | TGCAGGTGGAGGGCA[C/G]GGAGTGCCCAGCTCT | 10043 |
rs34371697 | snp | A/G | 0.000995289 | 0.0222857 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35330371 | CGCACGTGCCGAGCC[A/G]TGCAGCAGCGGGTCC | 10043 |
rs34472356 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35318777 | GGAGCCGTGGGCAGC[-/A]AGGAAGTGCTGCCAG | 10043 |
rs34490014 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338195 | GTAACCAAGCCACCT[-/C]CCCATGCTGCTGAGA | 10043 |
rs34511620 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335192 | CCACTGTGACCCCCA[-/G]GGCTGAGCTGTGGGC | 10043 |
rs34665221 | in-del | -/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35332376 | GGCTTCAGCACTTCA[-/G]GGGAGGCAGGTGCCT | 10043 |
rs34861948 | in-del | -/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301723 | ATCAATGCTCTCCAA[-/G]GGGGGAGGTGGCAGT | 10043 |
rs34874675 | in-del | -/G | | | intron-variant, nc-transcript-variant | TOM1, MIR3909 | GRCh38.p7 | 22:35335719 | GGAACTTGTCCTCTA[-/G]GGCCTGCAGTCTCAT | 10043 |
rs35017033 | in-del | -/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35320285 | TGTGGAGGTCAGGAG[-/C]CTTCAGGGTGCAAGT | 10043 |
rs35088389 | in-del | -/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301812 | CCCCTGCCCTCCCCG[-/T]GACACACACCCACCC | 10043 |
rs35231297 | in-del | -/T | | | intron-variant, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299495 | GGCTGTCACCCAGGG[-/T]TAGGTGTGCAGTCAC | 10043 |
rs35252840 | in-del | -/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35328711 | CCCGGAGGCCTGACC[-/T]TTGGAGGGGGCAGGG | 10043 |
rs35256950 | in-del | -/G | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297449 | GTAATCAGTTTGCAT[-/G]GGAGTTGTTTTTCTT | 10043 |
rs35266821 | in-del | -/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35340571 | GGCAACATGGGGAAA[-/C]CCCCATCTCTACAAA | 10043 |
rs35352978 | snp | A/G | 0.00117463 | 0.0242061 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35330383 | GCCATGCAGCAGCGG[A/G]TCCTGGAGCTCATCC | 10043 |
rs35502404 | in-del | -/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35307473 | TAAGCAGCCTGAAAT[-/G]GGGGTCACAGCTTAG | 10043 |
rs35588735 | in-del | -/A | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35342140 | GTAAGACTGTATCTC[-/A]AAAAAAAAAGAAACA | 10043 |
rs35674662 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337913 | CCCAACACCTGCCCT[-/G]GGGCACCCCCACTGC | 10043 |
rs35797919 | in-del | -/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35340622 | ATGGTGGCGCACACC[-/T]TTTAGTCCCAGCTAC | 10043 |
rs35806010 | in-del | -/C | | | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334829 | AACACAGTGTCTCCA[-/C]CCCCCCGCCCCCCTC | 10043 |
rs35896033 | in-del | -/A | 0.476314 | 0.106217 | intron-variant | TOM1 | GRCh38.p7 | 22:35339904 | GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAGA | 10043 |
rs35967206 | in-del | -/G | | | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347884 | CTGTTCCTTCTGGCC[-/G]GGCACCACAGCACTG | 10043 |
rs36013730 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337888 | TCTTTCCCTGCAACA[-/G]GGGCTGGGTCCCCAA | 10043 |
rs36202473 | in-del | -/ACACACACAT | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35332598 | CTAACACACACACAC[-/ACACACACAT]ACACACACACAAATA | 10043 |
rs41282609 | snp | C/T | 0.0490535 | 0.14873 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348129 | CACCCAGCTACACTA[C/T]GCAGGTGCCGCCTCC | 10043 |
rs41282611 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348236 | TCCTCAAGGCACCTT[C/T]GTGCTGCTGTTCCAT | 10043 |
rs55677714 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | TOM1 | GRCh38.p7 | 22:35307526 | TTCAGGTGCCAGCTC[C/T]GCCCCTTCCCGGCTG | 10043 |
rs55688205 | snp | C/T | 0.0437281 | 0.141251 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337314 | GCCTTGCCCACAATG[C/T]GCCAAGCATGTCTTA | 10043 |
rs55945110 | snp | G/T | 0.0228947 | 0.104514 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297841 | TGTTTTTTTTTGTTT[G/T]TTTTTTTTTTTTTTT | 10043 |
rs55958250 | snp | G/T | 0.0285273 | 0.115974 | intron-variant | TOM1 | GRCh38.p7 | 22:35345830 | GCAGGAGGACCCGTT[G/T]TTCTCACCAAGAAAT | 10043 |
rs56083910 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35331128 | TGAGGCACGATCTTG[A/C]TCTGTCACCCAGGCT | 10043 |
rs56099537 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35331130 | AGGCACGATCTTGCT[A/C]TGTCACCCAGGCTGG | 10043 |
rs56143758 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | TOM1 | GRCh38.p7 | 22:35323313 | CTCGGTTGTCGGCTG[C/G]TGGGATGTTCTGTGG | 10043 |
rs56264523 | snp | C/T | 0.0267979 | 0.112609 | intron-variant, downstream-variant-500B | TOM1, MIR3909 | GRCh38.p7 | 22:35335774 | ACCGCTGTGAAGGGC[C/T]AAGTGCTGTCCTGGA | 10043 |
rs56358602 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TOM1 | GRCh38.p7 | 22:35306303 | ACTGTTCCTCAAAGT[A/G]GGGTACCAGAGCACC | 10043 |
rs56376199 | in-del | -/G | | | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334717 | TCTGATCAGAGGGGG[-/G]AAACTGAGGCACAGA | 10043 |
rs56386030 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337330 | GCCAAGCATGTCTTA[A/G]AGACAGCAACAAGCA | 10043 |
rs57098663 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TOM1 | GRCh38.p7 | 22:35318214 | AGCCCAGATTCCACA[C/T]GGATCTGGAAGCCCA | 10043 |
rs57179954 | in-del | -/TA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35332607 | ACACACACACACACA[-/TA]CACACACACAAATAT | 10043 |
rs57403287 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35341746 | CTACCTTGCAGCCCG[A/C]CCACAGGGAGGAAAC | 10043 |
rs57705338 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | TOM1 | GRCh38.p7 | 22:35306379 | GTGAGCCCTAATATC[G/T]TGAAGCTTCTGTTTC | 10043 |
rs57755951 | snp | C/T | 0.00888988 | 0.066075 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35317938 | CATGGAGATCTGCGA[C/T]ATCATCAACGAGACG | 10043 |
rs58296927 | snp | C/T | 0.0142736 | 0.0832652 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297835 | TGTTTTTGTTTTTTT[C/T]TGTTTTTTTTTTTTT | 10043 |
rs58398866 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | TOM1 | GRCh38.p7 | 22:35302056 | AATCAAAGCAAACTT[C/T]TCTTCTTACCTTGAA | 10043 |
rs58401864 | in-del | -/AA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35324435 | AAAAAAAAAAAAAAA[-/AA]GGCTTCATTTGAAGA | 10043 |
rs58521435 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338173 | CCCAGAGGACATTTA[A/G]AAGAGCTGTAACCAA | 10043 |
rs58551595 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | TOM1 | GRCh38.p7 | 22:35321222 | GCCTCCAGGTTATTT[G/T]TTCTTAAACTTGAGC | 10043 |
rs59583460 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | TOM1 | GRCh38.p7 | 22:35316629 | CTGCAGCCGACTCCC[A/G]GCCTGGAAATCTTAC | 10043 |
rs59654138 | snp | A/G | 0.138207 | 0.223612 | intron-variant | TOM1 | GRCh38.p7 | 22:35306446 | AGTTTCTGTCTTGAG[A/G]ATGACAGAGCTTTGT | 10043 |
rs59869158 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | TOM1 | GRCh38.p7 | 22:35322823 | ACACCATACCTCTGC[C/T]CACCCTAGGCCGTGC | 10043 |
rs59940597 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TOM1 | GRCh38.p7 | 22:35300511 | CGGCCAGGCCTCACA[A/G]ACCCGGGTCTCAGGA | 10043 |
rs60243205 | in-del | -/G | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297853 | TTTTTTTTTTTTTTT[-/G]TTTTTACCATGAATA | 10043 |
rs60248459 | snp | C/T | 0.00458706 | 0.0476706 | intron-variant | TOM1 | GRCh38.p7 | 22:35318011 | ACGGCCATCCCACCA[C/T]GCAGCACACTCCTGC | 10043 |
rs60298343 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | TOM1 | GRCh38.p7 | 22:35310586 | AGGATTGCAAGTTGG[A/G]AGAAGGATTAGGATT | 10043 |
rs60452720 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | TOM1 | GRCh38.p7 | 22:35315196 | TGGCCGGGCTGGGGC[A/G]GGGGCAGTGGCAGAG | 10043 |
rs60784411 | snp | A/G | 0.0345262 | 0.126772 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348296 | ACTAATCACAAGGGC[A/G]GGGACCTGTGTGGAC | 10043 |
rs60822395 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TOM1 | GRCh38.p7 | 22:35328131 | GCGCTGTGTCTTCCT[C/T]GCCACCGTGTCTGTG | 10043 |
rs60840354 | in-del | -/TACACACA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35332607 | ACACACACACACACA[-/TACACACA]CACAAATATGTAATT | 10043 |
rs60871265 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | TOM1 | GRCh38.p7 | 22:35341583 | GCCACCTGGCCTCTC[A/G]TGGTCAGAGGTTGAC | 10043 |
rs61427661 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | TOM1 | GRCh38.p7 | 22:35315097 | AGGTTTCAGAAAGTT[C/T]CTTCTGGACAGTGTG | 10043 |
rs61429489 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35302355 | TTTTTTTTTTTTTGA[A/G]ACTGCGTTTCGCTCT | 10043 |
rs61675526 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TOM1 | GRCh38.p7 | 22:35314138 | ATCCACATGATTCAC[C/T]GCAATCCTGTTGTCC | 10043 |
rs61692841 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35312244 | ACAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 10043 |
rs61731672 | snp | A/G | 0.277778 | 0.248452 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35322007 | AATCGTGGGGAATAA[A/G]AACTTCCACGAGGTG | 10043 |
rs61731679 | snp | A/G | 0.00657196 | 0.0569455 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35327327 | CGTGAGGGTGATGTC[A/G]GAGATGCTGACGGAG | 10043 |
rs62233299 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304676 | GTAGAGACGGGGTTT[C/T]ACCGTGTTAGCCAGG | 10043 |
rs62233300 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35321004 | AAAAAAAAAAAAACT[A/T]GAATGGAAGGGTAAA | 10043 |
rs62233301 | snp | C/T | 0.150333 | 0.229274 | intron-variant | TOM1 | GRCh38.p7 | 22:35322297 | AGGGAGAGCCTGGGC[C/T]AAAGGACCTGTGGGT | 10043 |
rs62233312 | snp | A/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35330136 | TACAAAAAAAAAAAT[A/T]AGCCAGGCGTGGTGG | 10043 |
rs62233313 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | TOM1 | GRCh38.p7 | 22:35332883 | ATCATAACCCACCGT[A/G]TTGATGTTGAGACCC | 10043 |
rs62233314 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35333663 | GGTGGGGCACTCGGG[G/T]TCACTGCCCCTGGCA | 10043 |
rs62233315 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337336 | CATGTCTTAGAGACA[A/G]CAACAAGCACCTCCA | 10043 |
rs62233316 | snp | C/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35341610 | TGACTCCACCACCCA[C/G]TGGGCAGCAATCCCA | 10043 |
rs62654769 | snp | C/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343305 | GCCCTACACACCACA[C/G]CTACACACCCATACA | 10043 |
rs66698303 | in-del | -/AGTGT/GAGTG | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305906 | TGTGTTGGTTAGCAG[-/AGTGT/GAGTG]ACTAGACCAGGGTCA | 10043 |
rs67667590 | in-del | -/AT | | | intron-variant | TOM1 | GRCh38.p7 | 22:35332606 | CACACACACACACAC[-/AT]ACACACACACAAATA | 10043 |
rs70944256 | multinucleotide-polymorphism | GA/TG | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35305729 | AGGGCTCCAAGGGCA[GA/TG]GTGTGTGGTTACAGG | 10043 |
rs71191358 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35342143 | AGACTGTATCTCAAA[-/A]AAAAAAGAAACAGAA | 10043 |
rs71322668 | in-del | ACCTCCAGTCATACACCTACACACACAG/CAGCCGCCACATCCACCACACACA | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35342695 | CTCATCCCTCTACAC[lengthTooLong]CCTCCACACACCACA | 10043 |
rs72568088 | in-del | -/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301810 | GACCCCTGCCCTCCC[-/T]CGGACACACACCCAC | 10043 |
rs73170193 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | TOM1 | GRCh38.p7 | 22:35303110 | ACTGGAATCACAAAG[G/T]TCTCATCCACCTCCC | 10043 |
rs73170199 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | TOM1 | GRCh38.p7 | 22:35312576 | TGTGACTGCAGGCAA[A/G]TTGCTGCCTTCTCCA | 10043 |
rs73170200 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35315569 | CTGTCTCTCAGCCCT[A/G]TCAGAGGAGCTTTCC | 10043 |
rs73170201 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35315674 | GCCACCCTGGCATCC[A/G]TCTGGCTCAGGACCT | 10043 |
rs73172703 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35319105 | GAGTGAGGGTGAGGG[A/T]AGGAGTGGTGGGCAG | 10043 |
rs73402467 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant | TOM1 | GRCh38.p7 | 22:35310670 | ATTTACACTGTTATA[A/T]AGGTTTATTGTGCTG | 10043 |
rs73402468 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | TOM1 | GRCh38.p7 | 22:35311258 | GTGGGAAGGCCAGGG[A/C]AGCTGGACCTCACTC | 10043 |
rs73402470 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TOM1 | GRCh38.p7 | 22:35311604 | GTAATGCCCCCCTCT[A/G]CTCTGTTGCACCAGA | 10043 |
rs73402471 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TOM1 | GRCh38.p7 | 22:35312438 | GGATTTGCTCACTGA[C/T]GTCTCCCTGTAGCCT | 10043 |
rs73402477 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TOM1 | GRCh38.p7 | 22:35315820 | CCTCCTCTGTCCTCC[A/G]GCAGACTGGGTTTAG | 10043 |
rs73402487 | snp | C/T | 0.0785177 | 0.181917 | intron-variant | TOM1 | GRCh38.p7 | 22:35325098 | TTTTGGCTGCTGGGG[C/T]GGGGGCAGAGGCCTG | 10043 |
rs73402494 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TOM1 | GRCh38.p7 | 22:35332106 | TGTGTCTTTCTCCAT[C/T]AAAAGACACTCACTG | 10043 |
rs73402496 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35333849 | AGGGAGCTCGTGTAT[A/G]AGAAGCGCTTAGACC | 10043 |
rs73406712 | snp | A/G | 0.030665 | 0.119967 | intron-variant | TOM1 | GRCh38.p7 | 22:35340315 | AAGTGAAGCTCTATG[A/G]GTATATAGCAGGGAC | 10043 |
rs73406724 | snp | A/C/G | 0.0103295 | 0.0711199 | intron-variant | TOM1 | GRCh38.p7 | 22:35344843 | TGCTAAGCTTTTGAC[A/C/G]TCCCATTTCATCCTC | 10043 |
rs73885905 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | TOM1 | GRCh38.p7 | 22:35302255 | GGGCCCCAACCCCAG[A/C]GTTTCTGACTCTCCA | 10043 |
rs73885909 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TOM1 | GRCh38.p7 | 22:35309926 | TGGCCAGAAGTCCCA[A/G]GGCTACTTCTGGCTG | 10043 |
rs73885910 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | TOM1 | GRCh38.p7 | 22:35312727 | ATGAGCCTGACTGAA[G/T]GAGGAATGGCATTGC | 10043 |
rs73885911 | snp | C/T | 0.0287284 | 0.116357 | intron-variant | TOM1 | GRCh38.p7 | 22:35313867 | TTGCAGGGCCCGGTT[C/T]TGTCAGGAGCTGGAA | 10043 |
rs73885914 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TOM1 | GRCh38.p7 | 22:35325495 | ATACATTTCTGTTAC[A/G]TTAGGATTGGAGACA | 10043 |
rs73885915 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | TOM1 | GRCh38.p7 | 22:35326822 | GAGGAGAGAGAGGGG[G/T]GGATCCCAGTCTTCT | 10043 |
rs73885919 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35344164 | TGGCCCTGGCGCTGC[C/T]GTCCCTCCGCCATCA | 10043 |
rs73885920 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | TOM1 | GRCh38.p7 | 22:35346075 | GCTAGAGAGGCTAAC[C/T]GAGGAAGCATAACAG | 10043 |
rs74209384 | snp | C/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35342734 | CCTCCACACACCACA[C/G]CTCCACCCATACACC | 10043 |
rs74515727 | snp | A/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35324434 | AAAAAAAAAAAAAAA[A/G]AAGGCTTCATTTGAA | 10043 |
rs74517468 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35320987 | ACTCTGTCTCAGAAG[A/G]AAAAAAAAAAAAAAC | 10043 |
rs74525076 | snp | A/C | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35321001 | GGAAAAAAAAAAAAA[A/C]CTTGAATGGAAGGGT | 10043 |
rs74747041 | snp | C/T | 0.0490535 | 0.14873 | intron-variant | TOM1 | GRCh38.p7 | 22:35326444 | AAATGTTTCCCCAAG[C/T]CCAACTCCTTGGAAC | 10043 |
rs74767140 | snp | C/T | 0.084728 | 0.187577 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335109 | CCTTGCCGGGACCTG[C/T]GGGAGAACTGGCCCC | 10043 |
rs74775021 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35332332 | CTGTGCTTTCAAGCT[C/T]GCAGTCACTTATACC | 10043 |
rs74846012 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35301702 | GTGGCTCTTCCGAGG[C/T]TTTGTAATCAATGCT | 10043 |
rs74856028 | snp | A/C/G | 0.0127048 | 0.0787486 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334841 | TCCACCCCCCGCCCC[A/C/G]CTCCCTGCACTGTGT | 10043 |
rs74928174 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298452 | TTGTTTTTTTTTTTA[A/G]GACACAGCCTTACTC | 10043 |
rs74956557 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TOM1 | GRCh38.p7 | 22:35307661 | GGGCCTCGCTCCTGC[C/T]GGGGAAGGTAGAGAA | 10043 |
rs74997631 | snp | A/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35301272 | CGCACACATATATAT[A/T]AAAATATACACATAC | 10043 |
rs75034965 | snp | A/G | 0.206642 | 0.246211 | intron-variant | TOM1 | GRCh38.p7 | 22:35314238 | CACAGCCTCCCAACA[A/G]CTGTCTTGTACTGGA | 10043 |
rs75303553 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35309239 | ACTGAGGCACAGAGA[G/T]GCCGAGGAGTTACCC | 10043 |
rs75527514 | snp | A/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35324437 | AAAAAAAAAAAAAAA[A/G]GCTTCATTTGAAGAG | 10043 |
rs75529622 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35308147 | CTGCCAGCTCACCCT[A/G]CAGATTTTCAACTTG | 10043 |
rs75619306 | snp | A/C | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35305660 | TGAGACTCAATCTCA[A/C]AAAAAAAAAAAAAAC | 10043 |
rs75757770 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304139 | GCTTTCCAGGGTTCC[A/C]CAGCCACTCAAGGTC | 10043 |
rs76054329 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334616 | CTGGGAGCCCTGTGG[A/T]CAGTTGACAGACTGC | 10043 |
rs76212089 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35332554 | AGATTAGAGATACAT[A/G]TATCTTTCTTACAGC | 10043 |
rs76293598 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35303823 | ATTTCTACCCTCATT[A/G]TACTAATATGCCACC | 10043 |
rs76419198 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35344048 | ACCTACATACACACC[C/T]TTACACACCTACACA | 10043 |
rs76516635 | snp | A/G | 0.0785177 | 0.181917 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337729 | CCCCGCTTCACTAGC[A/G]TGTCAGGTGGCCTTG | 10043 |
rs76640031 | snp | C/T | 0.0399052 | 0.1355 | intron-variant | TOM1 | GRCh38.p7 | 22:35314324 | TTCTCGTTTAGGCCA[C/T]ATATCCCCTCCCACC | 10043 |
rs76709046 | snp | G/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35321352 | TCTGCTTTTTTTTTT[G/T]GAATGTCCTTTGTTT | 10043 |
rs76951410 | snp | G/T | 0.0150606 | 0.0854603 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297280 | CCACCTACTCAAGAG[G/T]CTGAAGTGGGAAGAC | 10043 |
rs76960113 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TOM1 | GRCh38.p7 | 22:35312132 | CGCCTGTAATCCCAG[C/T]TACTTTGGGGGCTGA | 10043 |
rs76975453 | snp | C/T | 0.0836354 | 0.186609 | intron-variant | TOM1 | GRCh38.p7 | 22:35303990 | AGAAAAGGAAAGTAA[C/T]ATTTTGTGAGCAAAC | 10043 |
rs76982037 | snp | A/C | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35300906 | CCATATAAAAAAAAA[A/C]AGTTGTAATATTTAT | 10043 |
rs77155265 | snp | C/T | 0.139564 | 0.224285 | intron-variant | TOM1 | GRCh38.p7 | 22:35303272 | GGCTTGCCCCAAGCC[C/T]GACGTTGCTCTTTTA | 10043 |
rs77207685 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35321878 | GATGGGCCAATAAGA[A/G]CTGTTCCAACTCTCC | 10043 |
rs77287354 | snp | C/T | 0.0792508 | 0.182605 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337399 | AAGTCAGCAACCTGA[C/T]GCCCCACCTCCCCCG | 10043 |
rs77376022 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TOM1 | GRCh38.p7 | 22:35344494 | CCTGCTCTTGAGTCT[C/T]GGGCAAGGACAAGGT | 10043 |
rs77483862 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35302389 | TGCCCAGGCTGGGGT[A/G]CAATGGCACCATCTT | 10043 |
rs77509118 | snp | C/T | 0.0770498 | 0.180522 | intron-variant, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299549 | CTATGACCCTAAGAG[C/T]CTCGGCTTCTGTGTA | 10043 |
rs77557948 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TOM1 | GRCh38.p7 | 22:35326128 | AGCAATATATGTTCA[A/G]TGCTTGGCACTTATT | 10043 |
rs77565301 | in-del | -/AAA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35323398 | GTTAAAAAAAAAAAA[-/AAA]GCAGGGAAAGAATGT | 10043 |
rs77584677 | snp | G/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35321353 | CTGCTTTTTTTTTTT[G/T]AATGTCCTTTGTTTT | 10043 |
rs77585216 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35340016 | CCACTTGTCCAGCAC[C/T]GAGCACATTTTGTGG | 10043 |
rs77644346 | snp | C/T | 0.0832709 | 0.186283 | intron-variant | TOM1 | GRCh38.p7 | 22:35318986 | GGGAGGCTGTGGGCA[C/T]CTGAGTCACACAGTC | 10043 |
rs77796077 | snp | A/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35330134 | ACTACAAAAAAAAAA[A/T]TTAGCCAGGCGTGGT | 10043 |
rs77884445 | snp | A/G | 0.5 | 0 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35330456 | TCAATGACAATCTCA[A/G]CAATGTGTTCCTGCG | 10043 |
rs77970897 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35308275 | GCTAGTTCCTTTTCT[C/T]TTTTTTTTTTTTTTT | 10043 |
rs78215045 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35300288 | GGGAGAAAGTTTTCG[C/T]GGTTAAAGGGACTGC | 10043 |
rs78347733 | in-del | -/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35316794 | CGCCTCAACTTTTTT[-/T]AAAAAGAACCACCAC | 10043 |
rs78347920 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | TOM1 | GRCh38.p7 | 22:35327877 | AGCTAGTGGTTCCTG[C/T]TCCCGGGTGTCACAT | 10043 |
rs78379716 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | TOM1 | GRCh38.p7 | 22:35310577 | TGTATTCAGAGGATT[A/G]CAAGTTGGAAGAAGG | 10043 |
rs78408805 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | TOM1 | GRCh38.p7 | 22:35332676 | TACTGCGTGCCATGC[A/T]TTCCTATTTTCTTTG | 10043 |
rs78603240 | snp | A/C | 0.0236746 | 0.106192 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334862 | TGCACTGTGTACCGC[A/C]TAGTAAGCCCTCCAG | 10043 |
rs78671239 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TOM1 | GRCh38.p7 | 22:35307665 | CTCGCTCCTGCTGGG[C/G]AAGGTAGAGAAGGGA | 10043 |
rs78771622 | snp | A/G | 0.093777 | 0.195178 | intron-variant | TOM1 | GRCh38.p7 | 22:35329813 | ACCGGCAGCACAGTT[A/G]GACATGTTGATGGTT | 10043 |
rs78817003 | snp | A/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35320986 | GACTCTGTCTCAGAA[A/G]GAAAAAAAAAAAAAA | 10043 |
rs78869242 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35308291 | TTTTTTTTTTTTTTT[C/T]TTTTTTTTTTGAGAC | 10043 |
rs78955559 | snp | A/G | 0.081446 | 0.184634 | intron-variant | TOM1 | GRCh38.p7 | 22:35344354 | GCTCTCCAAGGGAGT[A/G]GGACCCAGGAGAAGG | 10043 |
rs79603137 | snp | A/C | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35330279 | AGAGCTCCGTCTCAC[A/C]AAAAAAAAAAGAGAC | 10043 |
rs79632383 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35303826 | TCTACCCTCATTATA[C/T]TAATATGCCACCGTC | 10043 |
rs79664333 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TOM1 | GRCh38.p7 | 22:35328539 | CTGCGATTTGAACCC[A/G]GGGGCCTGGCTCCAA | 10043 |
rs79707159 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35344610 | TGCTGCTGGGAAGTC[A/G]GCTCCTGCCTTCTCT | 10043 |
rs79723408 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | TOM1 | GRCh38.p7 | 22:35312529 | GAACCAGACTTCTCT[A/G]GCTTTGAATCTGCTG | 10043 |
rs79840063 | snp | A/G | 0.102014 | 0.201495 | intron-variant | TOM1 | GRCh38.p7 | 22:35329801 | AAGCCAAGTTAAACC[A/G]GCAGCACAGTTGGAC | 10043 |
rs79872497 | snp | C/G | 0.0626037 | 0.165477 | intron-variant | TOM1 | GRCh38.p7 | 22:35315260 | ACTTGGCAGGACTTC[C/G]TGGCCTTTAGGTGTG | 10043 |
rs79884643 | snp | G/T | 0.139225 | 0.224118 | intron-variant | TOM1 | GRCh38.p7 | 22:35303111 | CTGGAATCACAAAGT[G/T]CTCATCCACCTCCCC | 10043 |
rs79909268 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | TOM1 | GRCh38.p7 | 22:35309558 | CTGAGACAGGAGAAT[A/C]GCTTGAACCGGTGAG | 10043 |
rs79999446 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35324438 | AAAAAAAAAAAAAAG[A/G]CTTCATTTGAAGAGA | 10043 |
rs80067987 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | TOM1 | GRCh38.p7 | 22:35301370 | CACCAAGTGAAGGTT[A/G]GGAATCCCTGGAAAT | 10043 |
rs80146635 | in-del | -/TACACACACA | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35332607 | ACACACACACACACA[-/TACACACACA]CAAATATGTAATTGA | 10043 |
rs80332714 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | TOM1 | GRCh38.p7 | 22:35308199 | AGCCAATTCCTTAAG[C/T]GCTCGCTCTTTCTCC | 10043 |
rs80343409 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298450 | GTTTGTTTTTTTTTT[A/T]AAGACACAGCCTTAC | 10043 |
rs111066936 | snp | A/C | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343334 | CACCTACACACCCCC[A/C]CACACACACCACACA | 10043 |
rs111163932 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35342928 | CACCTCCACACGTCA[C/T]ACCTCCACTCATACA | 10043 |
rs111163933 | snp | C/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343387 | CCACACACACCTCCA[C/G]TCATAAACCTACACA | 10043 |
rs111163934 | snp | A/C | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343393 | ACACCTCCACTCATA[A/C]ACCTACACACACAGC | 10043 |
rs111165352 | snp | C/T | 0.43555 | 0.167544 | intron-variant | TOM1 | GRCh38.p7 | 22:35343022 | ACACACATCTACACC[C/T]ACCACACACACCTCC | 10043 |
rs111165353 | snp | C/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343270 | CTCCACACACCTCCA[C/G]TCATACACCTACACA | 10043 |
rs111165354 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343649 | CACACACCACACCTA[C/T]ACTCATACACCTACA | 10043 |
rs111165355 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343672 | CACCTACACACACCC[C/T]TACACACACCACACC | 10043 |
rs111213306 | snp | A/C | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343596 | TACACCTACACACAC[A/C]CCTACACACACCACA | 10043 |
rs111213307 | snp | A/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35343695 | ACCACACCTACACAC[A/T]CATACACCTACACAC | 10043 |
rs111220638 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343089 | CCTACACACACCACA[C/G]CTACACACCCATACA | 10043 |
rs111220663 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343795 | CACACCACACACCTA[C/T]ACCTACCCACACCTA | 10043 |
rs111325167 | snp | A/C | 0.0825414 | 0.185628 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334850 | CGCCCCCCTCCCTGC[A/C]CTGTGTACCGCATAG | 10043 |
rs111336728 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35342904 | ACACACATCTACACC[C/T]ACCACACACACCTCC | 10043 |
rs111396171 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35322247 | CAATCCCCCAGCATG[A/G]GAACAGACGCTTACA | 10043 |
rs111476686 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334199 | GCAGGTGGCCTGCCT[C/T]GCGCATTCCCCCACC | 10043 |
rs111480148 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35310743 | GTACTGCAGGTTTAT[C/G]ATGGCCCAGGTCCCA | 10043 |
rs111532519 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35326788 | TAGGAGGAGAGAGGG[C/T]GGGATCCCAGTCCTC | 10043 |
rs111574753 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35339777 | GGCGTGGTGGCGGGC[G/T]CCTGTAGTCCCAGCT | 10043 |
rs111711285 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35340480 | GGCCGGGCACAGTGG[A/C]TCACACCTGGAATCC | 10043 |
rs111716568 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TOM1 | GRCh38.p7 | 22:35319123 | GAGTGGTGGGCAGAG[A/G]TCAGAAGAAAGAAAG | 10043 |
rs111823603 | snp | C/T | 5.50555e-05 | 0.0052464 | intron-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35321838 | GAACCTGGCTGGATA[C/T]ACAAAACAGGTGGGG | 10043 |
rs112053870 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35323290 | CTCCGCTTCTCATTT[C/T]GGGGCGTCTCGGTTG | 10043 |
rs112145046 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | TOM1 | GRCh38.p7 | 22:35307323 | ATGGCTTTGATGTTC[A/G]TGTTTTTTTCCTATC | 10043 |
rs112187961 | snp | C/T | 0.021333 | 0.101051 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35336864 | CCACCACAGGCATGG[C/T]CTTCAGGGACAGCTG | 10043 |
rs112253992 | in-del | -/A | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35323385 | AGGGCAGATGTAGTT[-/A]AAAAAAAAAAAAAAA | 10043 |
rs112365391 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | TOM1 | GRCh38.p7 | 22:35317468 | GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC | 10043 |
rs112459699 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334688 | TGACCCACTGTATGC[C/G]AGAATCTTACATAGT | 10043 |
rs112513225 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35310355 | GTCAAGAGATCGAGA[C/G]CATCCTGGCCAATGT | 10043 |
rs112634351 | in-del | -/GAGTG | 0.498734 | 0.0251279 | intron-variant | TOM1 | GRCh38.p7 | 22:35305905 | CTGTGTTGGTTAGCA[-/GAGTG]AGACTAGACCAGGGT | 10043 |
rs112696008 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TOM1 | GRCh38.p7 | 22:35322168 | GGTCTGTAGGCAACG[C/T]ACTGTCCTGTCTACA | 10043 |
rs112701349 | snp | A/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35308204 | ATTCCTTAAGCGCTC[A/G]CTCTTTCTCCTGTGT | 10043 |
rs112705989 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35322342 | GTAAACCCAGGCCTC[C/T]GCGGGGGCAGGGAGG | 10043 |
rs112707607 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35346721 | GGAAAACACAAGGCT[C/T]AGGAAGTCAGGTGCC | 10043 |
rs112780125 | snp | A/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35309883 | CCTTCCCCAGGAGCC[A/G]CCCAAGAGACACCCG | 10043 |
rs112806242 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35315773 | AGCCAGCCTGGCTAG[A/G]AGAGGGCCCTGTCCA | 10043 |
rs112823782 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | TOM1 | GRCh38.p7 | 22:35311595 | CAAAAGTATGTAATG[C/T]CCCCCTCTGCTCTGT | 10043 |
rs112858628 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337093 | AGGCGCCCACCACCA[C/T]ACCTGGCTAATTTTT | 10043 |
rs112932071 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | TOM1 | GRCh38.p7 | 22:35314224 | CTGGGCAGATGTCCC[A/G]CAGCCTCCCAACAGC | 10043 |
rs112940137 | snp | A/C | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35324205 | GTGTTTTCTGCGGGG[A/C]CCTCCAACAGCACCA | 10043 |
rs113100190 | in-del | -/G | 0.133777 | 0.221342 | intron-variant | TOM1 | GRCh38.p7 | 22:35314457 | GCACGGGGTGGGGGC[-/G]GGGGGTCCTTCTGCT | 10043 |
rs113107433 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35309818 | TCTCACGGTAGGAAG[C/T]ACAGGTGAAAGTACC | 10043 |
rs113120019 | snp | C/T | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35324809 | CTCGTCTTGGCCTCC[C/T]AAAGTGCTGGGATTA | 10043 |
rs113154097 | snp | A/T | 0.0919752 | 0.193722 | intron-variant | TOM1 | GRCh38.p7 | 22:35333282 | TTCCCTGATGCCCAG[A/T]CCTAGCTCCTGGGGC | 10043 |
rs113168198 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35307235 | CCTTCATTATTATTT[C/T]CGTAGGGTTTTCTTT | 10043 |
rs113180491 | snp | A/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35300192 | GTGATAGATGTATAT[A/G]ACAGCCAGTAGGTAA | 10043 |
rs113181461 | snp | A/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35318241 | CCCAGCCTTGTGTGC[A/G]GCATCTGCCTAGGAT | 10043 |
rs113273925 | snp | A/G | 0.444444 | 0.157135 | intron-variant | TOM1 | GRCh38.p7 | 22:35332441 | GAACATAATTTACCC[A/G]AGGTCATGTGATAAG | 10043 |
rs113301082 | snp | A/C/T | 5.06445e-05 | 0.00503186 | intron-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35321817 | AGGAAGATTCTGATG[A/C/T]GATCAGAACCTGGCT | 10043 |
rs113307644 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35323279 | TTTGTCCCAGGCTCC[A/G]CTTCTCATTTCGGGG | 10043 |
rs113493230 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334219 | ATTCCCCCACCCACA[C/T]GTGCCACTTCCCCAG | 10043 |
rs113612209 | snp | A/G | 0.5 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35314840 | CCCTTACCTCTGTGT[A/G]CCCTTTGCAAGTTGG | 10043 |
rs113638947 | snp | A/G | | | intron-variant, splice-donor-variant | TOM1 | GRCh38.p7 | 22:35299981 | TGGGACAGCGCATCG[A/G]TGAGTCCCTGGAGCC | 10043 |
rs113676195 | in-del | -/TCATGAGA | 0.103794 | 0.20279 | intron-variant | TOM1 | GRCh38.p7 | 22:35314879 | TGTGCTTCAGTTTCC[-/TCATGAGA]TCATGAGATGAGGGC | 10043 |
rs113746839 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TOM1 | GRCh38.p7 | 22:35312815 | ACTGTGGCTGACGCC[A/G]GCCCCTGGAGAGTTC | 10043 |
rs113856063 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35311335 | GGAAACGCAACCAGC[A/G]GAGTCTGAAACCACC | 10043 |
rs113925847 | snp | A/C/G | 0.00923213 | 0.0673162 | intron-variant | TOM1 | GRCh38.p7 | 22:35300021 | TCCGCCCCGGTGCTC[A/C/G]GCACCCAGCTTCGGT | 10043 |
rs114006544 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35341348 | TTACAGATGAGAAAA[C/T]TGAGGCTGAGGACAG | 10043 |
rs114106185 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | TOM1 | GRCh38.p7 | 22:35342412 | GCCCTAGGAAACTGC[A/C]TGTGTGCCATGGATG | 10043 |
rs114222736 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | TOM1 | GRCh38.p7 | 22:35342687 | ATACCTGCCTCATCC[A/C]TCTACACCAGCCGCC | 10043 |
rs114269151 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TOM1 | GRCh38.p7 | 22:35303804 | CGCTTGGCTTATTTT[C/T]ATTATTTCTACCCTC | 10043 |
rs114276307 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35329656 | TCTAGTTCATTCTGT[A/G]TGCTTTGGTTGCAAA | 10043 |
rs114302892 | snp | G/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335411 | CCCTGGCTGTTAGCT[G/T]TATCTTTCTTTAGTC | 10043 |
rs114513194 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | TOM1 | GRCh38.p7 | 22:35300322 | GTTGGCAGTGGCTGG[A/G]CCACTCTGCTGGGTC | 10043 |
rs114547806 | snp | A/T | 0.0490535 | 0.14873 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334204 | TGGCCTGCCTCGCGC[A/T]TTCCCCCACCCACAC | 10043 |
rs114613375 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35328430 | GGTTCACATCGCTCA[C/T]GTAATCCTGACCACC | 10043 |
rs114628428 | snp | C/T | 0.0588605 | 0.161139 | intron-variant | TOM1 | GRCh38.p7 | 22:35346769 | CGGCTCAGGGAGGAG[C/T]CCAGGTCCAGGTCCT | 10043 |
rs114740270 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35327559 | GATTGGAATCAGATC[A/G]CAGCTCTACCACTTT | 10043 |
rs115041411 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35333853 | AGCTCGTGTATGAGA[A/C]GCGCTTAGACCATGC | 10043 |
rs115068977 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35311869 | ATTGTTCTCCATGAT[A/G]TTGTTATTGTCATGG | 10043 |
rs115453758 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35342828 | ACACCTACACAGACA[A/C]CCCTACACACACACC | 10043 |
rs115531707 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | TOM1 | GRCh38.p7 | 22:35300515 | CAGGCCTCACAGACC[C/T]GGGTCTCAGGACGTG | 10043 |
rs115540450 | snp | A/G | 0.00363513 | 0.0424776 | intron-variant | TOM1 | GRCh38.p7 | 22:35327252 | GGCTTCTCTCACCAC[A/G]ATCAACTGTGTGTTT | 10043 |
rs115621935 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | TOM1 | GRCh38.p7 | 22:35305261 | CCATCTCCCCTATTG[A/G]CAACACAGAGGTGCT | 10043 |
rs115654601 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TOM1 | GRCh38.p7 | 22:35342688 | TACCTGCCTCATCCC[C/T]CTACACCAGCCGCCA | 10043 |
rs115702293 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35305860 | GTGAAGGCAGAAGCC[A/G]GGGTGGGGAGGGCGA | 10043 |
rs115755221 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | TOM1 | GRCh38.p7 | 22:35344496 | TGCTCTTGAGTCTCG[C/G]GCAAGGACAAGGTAG | 10043 |
rs115762946 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35340116 | GCTTTTCAGGCAGTG[A/T]GAGAATTTCTGCTCC | 10043 |
rs115820010 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35311965 | GGCTTAGAAGATGAG[A/G]GGAGTTCGGCTGGGC | 10043 |
rs115889266 | snp | A/G | 0.00953873 | 0.0683987 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348089 | GAGCATCTGTAGATG[A/G]TGCAGGCGGAAGGAC | 10043 |
rs115951602 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | TOM1 | GRCh38.p7 | 22:35344055 | TACACACCCTTACAC[A/C]CCTACACACACCCCT | 10043 |
rs116127822 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | TOM1 | GRCh38.p7 | 22:35332150 | CAGTGGAAAGTGGGG[G/T]GTACCCTGCAGGTCA | 10043 |
rs116159305 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | TOM1 | GRCh38.p7 | 22:35310959 | AGGCCCTGGCGGGGT[A/G]GGGGGTGTCAGGGCA | 10043 |
rs116191446 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35340144 | TCCAGCAAGTGAGCA[A/G]ACAGAGCAGGTCCCA | 10043 |
rs116267779 | snp | A/G | 0.155987 | 0.23165 | intron-variant | TOM1 | GRCh38.p7 | 22:35342929 | ACCTCCACACGTCAT[A/G]CCTCCACTCATACAC | 10043 |
rs116279387 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299412 | CGAGCAGGGTGCATC[C/T]TGGAGCGGGGAGACC | 10043 |
rs116530030 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | TOM1 | GRCh38.p7 | 22:35326470 | GGAACCCTTTGACCA[C/T]TGAAAACCTGCCCAC | 10043 |
rs116597340 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35340820 | GTGGGCAAAGTCTTC[A/G]TGACCCCCAAGGGCA | 10043 |
rs116624461 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334261 | GGGTCTGGCAGCAGG[C/T]AGCTCAGCAGCAGCT | 10043 |
rs116653081 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35308799 | TGACATTTCCTTTTG[C/T]TAGGTACTATAGTTA | 10043 |
rs116691231 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35320310 | GCAAGTGGGGGCCCT[A/G]CACAAAGGCTTTTAG | 10043 |
rs116718567 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant, downstream-variant-500B | TOM1, MIR3909 | GRCh38.p7 | 22:35335964 | CCCGCACAGCAGCTG[G/T]GAAAGATGCTCTTCA | 10043 |
rs116912627 | snp | A/G | 0.0562307 | 0.157967 | intron-variant | TOM1 | GRCh38.p7 | 22:35323308 | GGCGTCTCGGTTGTC[A/G]GCTGGTGGGATGTTC | 10043 |
rs116966945 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TOM1 | GRCh38.p7 | 22:35342222 | CAGGACTCACAAGTC[A/G]TGTGACGAGGTGGTA | 10043 |
rs117019401 | snp | G/T | 0.0217236 | 0.101931 | intron-variant | TOM1 | GRCh38.p7 | 22:35317206 | CTTGTTTGTTTGTTT[G/T]TTTTGGAGATGGAGT | 10043 |
rs117039833 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | TOM1 | GRCh38.p7 | 22:35340738 | GGCAATGGAGTAAGA[C/T]CCTGTCTCAAGAAAA | 10043 |
rs117241128 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298263 | GCAAAACAGAAATAG[C/T]AGCCCAGCCCCCAGG | 10043 |
rs117299818 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35307041 | GTTTTAGAAAAAAAA[A/C]AACCCAAACCCTCAG | 10043 |
rs117352134 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TOM1 | GRCh38.p7 | 22:35326688 | CTAGGAGGAGAGAGA[A/G]AGGACGGAATCCCAG | 10043 |
rs117372481 | snp | A/C/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35328086 | GAGTTCCTACTGCTC[A/C/G]TCCACCAGGCCTCAG | 10043 |
rs117401936 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | TOM1 | GRCh38.p7 | 22:35309659 | AAAAAAAAAAAAAAA[A/G]AGAGAGAGAACTGAG | 10043 |
rs117508568 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35345041 | TGCCCCTGCAGAAGC[C/T]GTTAGAGAGGAAAGC | 10043 |
rs117557604 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TOM1 | GRCh38.p7 | 22:35306844 | CCTGGCAAATGAGCG[A/G]TCACTGGCTGGGTGG | 10043 |
rs117631997 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | TOM1 | GRCh38.p7 | 22:35327746 | GGGGTCCTGAGAAAA[A/G]GCTGGAAGGTGAGAT | 10043 |
rs117634594 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299111 | GCTCATGGCTTTTGT[C/G]AAATTCTCAAAGGAG | 10043 |
rs117670616 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35321245 | ACTTGAGCATGCATA[A/G]GAAACCCTTGGGGAG | 10043 |
rs117693126 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | TOM1 | GRCh38.p7 | 22:35343900 | ACCTACACACCTGCA[C/G]ACACACCCCTACACA | 10043 |
rs117696523 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | TOM1 | GRCh38.p7 | 22:35311424 | GTTTGACAGCTCCAC[A/G]ATGTCTCAAAACAGC | 10043 |
rs117718592 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | TOM1 | GRCh38.p7 | 22:35330821 | TTCCTGGTTCTGGGG[A/C]CTTAGACAAGTGACT | 10043 |
rs117763819 | snp | A/G | 0.000814921 | 0.0201692 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347097 | CCAAAGCCGCGGACC[A/G]ATTGCCCAACCTCTC | 10043 |
rs117811343 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | TOM1 | GRCh38.p7 | 22:35304183 | AGGTCTTCTTTTGTA[C/T]CCTCACCACACTGCC | 10043 |
rs117831641 | snp | C/G | 0.00993419 | 0.0697739 | intron-variant | TOM1 | GRCh38.p7 | 22:35326452 | CCCCAAGCCCAACTC[C/G]TTGGAACCCTTTGAC | 10043 |
rs117905007 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TOM1 | GRCh38.p7 | 22:35330828 | TTCTGGGGCCTTAGA[C/T]AAGTGACTTCACTGC | 10043 |
rs117934826 | snp | A/G | 0.0879971 | 0.190408 | intron-variant | TOM1 | GRCh38.p7 | 22:35303831 | CCTCATTATACTAAT[A/G]TGCCACCGTCCCACT | 10043 |
rs117971694 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | TOM1 | GRCh38.p7 | 22:35306711 | TCTCTGTAATTATTA[C/G]CTGTTGTGATTTTTC | 10043 |
rs118041376 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | TOM1 | GRCh38.p7 | 22:35343950 | CACCACCTACACACA[C/T]CACATACATCTATAC | 10043 |
rs137868113 | in-del | -/AA | 0.498693 | 0.0255257 | intron-variant | TOM1 | GRCh38.p7 | 22:35305659 | GTGAGACTCAATCTC[-/AA]AAAAAAAAAAAAAAC | 10043 |
rs137894733 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | TOM1 | GRCh38.p7 | 22:35305407 | TGGCTCACGCCTGTA[A/C]TCCCAGCACGTTGGG | 10043 |
rs138007360 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35340209 | CCAGGGAGTCCGGGG[C/G]AGTGAGGGTGGTGGA | 10043 |
rs138233115 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | TOM1 | GRCh38.p7 | 22:35325742 | TTCTGAAGTCTAGCA[C/T]CTGTGTGGATTAAGA | 10043 |
rs138395632 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35313313 | GATCGTGCCACTGTA[C/T]TCCAACCTGGGTGAC | 10043 |
rs138494157 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35302069 | TTCTCTTCTTACCTT[C/G]AAGCGTTGCCTTTCT | 10043 |
rs138533846 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35344678 | GGGTGACAGAGCTTG[A/G]AAACCAAACTGGCCT | 10043 |
rs138650002 | snp | C/T | 8.24056e-05 | 0.00641841 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334356 | CAGTGTGAGAGCTGG[C/T]CTGCAGTCTCTGGAG | 10043 |
rs138700309 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335062 | TCAGCAGCATAGGCA[C/T]GTGGCCTGAGTGTGT | 10043 |
rs138996094 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35330911 | AGGATAATAATCTTT[A/G]TTAAATGGGTAGCTT | 10043 |
rs139006374 | snp | G/T | 0.00178674 | 0.0298358 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35299961 | GAACCCGTTCAGCTC[G/T]CCAGTGGGACAGCGC | 10043 |
rs139041856 | snp | C/T | 1.64814e-05 | 0.00287061 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35327323 | GGAACGTGAGGGTGA[C/T]GTCGGAGATGCTGAC | 10043 |
rs139042198 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TOM1 | GRCh38.p7 | 22:35326590 | ATAGACCAGAAACAG[A/G]ACAAAATCCCAGTCC | 10043 |
rs139058644 | snp | C/G/T | 8.39686e-05 | 0.00647905 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323823 | TGGGCACTGACTCCA[C/G/T]CCAGCAAGAGGACTC | 10043 |
rs139066487 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35327635 | TAAGATTGCTCTAAC[A/G]ATAGCCTTCATGGCA | 10043 |
rs139098897 | snp | A/G | 0.000514463 | 0.0160302 | missense, nc-transcript-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338744 | CCCCAAGCAACAGAC[A/G]GCCTGGCTGGAGCCC | 10043 |
rs139147613 | snp | A/G | 4.99546e-05 | 0.00499748 | missense, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323035 | CCCTCCAGGTCTTAG[A/G]AACCTGTGTCAAGAA | 10043 |
rs139185210 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35332666 | TCCTTACCTTTACTG[C/T]GTGCCATGCATTCCT | 10043 |
rs139259966 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338649 | TGTGCCCCCCAGCCC[A/G]CTCCGTTCTTGCATC | 10043 |
rs139285675 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35341082 | CTCCAGTCCTTTTTC[A/G]GGTGTAAGCCATCAT | 10043 |
rs139327284 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35341459 | GCCCTAAGGTGCAAA[C/G]GAGAGTGAGTGGAGG | 10043 |
rs139364161 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | TOM1 | GRCh38.p7 | 22:35302620 | TACAGGCATGACCAC[C/T]GTGTCCGGCCTAGAA | 10043 |
rs139457306 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298523 | CTGCAATCTCTGCCC[C/G]CCTGGGTCCAAGCAA | 10043 |
rs139553640 | in-del | -/AAAAA | 0.0517044 | 0.152246 | intron-variant | TOM1 | GRCh38.p7 | 22:35301065 | aaaaaaaaaaaaaaa[-/AAAAA]tacagaaattagccg | 10043 |
rs139602163 | in-del | -/GGATCCTTGT | 0.0998734 | 0.199905 | intron-variant | TOM1 | GRCh38.p7 | 22:35342554 | GAGGCCCAGCCTCTG[-/GGATCCTTGT]GGATCCTTGTGGAGA | 10043 |
rs139668404 | in-del | -/GA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35326906 | CCAGTCCTCTAGTGG[-/GA]GAGAGAGAGAGGGCC | 10043 |
rs139699618 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35315380 | TTAACACTGACTGAC[A/G]TGACTAACCCCCGCC | 10043 |
rs139733763 | snp | C/G/T | 0.00111994 | 0.0236375 | intron-variant | TOM1 | GRCh38.p7 | 22:35321922 | TTAGGTAAGGGGGCT[C/G/T]TATTCCTAAGCCCAC | 10043 |
rs139784161 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TOM1 | GRCh38.p7 | 22:35315949 | AGCCGTGTAGCAAGC[A/G]AAGAGTCACCCACCC | 10043 |
rs139851289 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TOM1 | GRCh38.p7 | 22:35317000 | CTGTTAGTAATGGAG[C/T]GTTTGCTTCCTAGGT | 10043 |
rs139858272 | snp | C/T | 8.25655e-05 | 0.00642463 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323507 | TCAGTCCTGGGCTGA[C/T]GCGTTCCGCAGCTCG | 10043 |
rs139926709 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35303155 | ACACACACACCCCTT[G/T]GTGCTTGCTGGTCCC | 10043 |
rs140031121 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TOM1 | GRCh38.p7 | 22:35309738 | ATGAATTCGTTCAGT[A/T]GTGGCTTCTTCTGTA | 10043 |
rs140049977 | in-del | -/TCTG | 0.0260105 | 0.111035 | intron-variant | TOM1 | GRCh38.p7 | 22:35344708 | TGGTTGGGGAAAGAC[-/TCTG]TCTGTCTTTTCCAAA | 10043 |
rs140060230 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337311 | TCAGCCTTGCCCACA[A/G]TGCGCCAAGCATGTC | 10043 |
rs140072090 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | TOM1 | GRCh38.p7 | 22:35317477 | ACAGGCGTGAGCCAC[C/T]GCGCCCAGCTCAAAA | 10043 |
rs140122879 | snp | A/C/T | 0.00319098 | 0.0398384 | intron-variant | TOM1 | GRCh38.p7 | 22:35322255 | CAGCATGGGAACAGA[A/C/T]GCTTACATCACTCCA | 10043 |
rs140278929 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TOM1 | GRCh38.p7 | 22:35328053 | CATGAGGAGACAGAG[C/T]GCTTCGTGTAACTGT | 10043 |
rs140300505 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35331091 | CACAAACACCTGTCC[-/A]CCTTTTTTTTTTTTT | 10043 |
rs140449290 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TOM1 | GRCh38.p7 | 22:35332217 | AATGAAAGGCCTCTT[C/T]CCTGCCATTTTGGGG | 10043 |
rs140458128 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301315 | ACATACACATACATA[C/T]ATATTATATGTATTT | 10043 |
rs140465923 | snp | C/T | 0.00770379 | 0.0615836 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347185 | GACCCAGGAGAAAGA[C/T]GATGACATGCTGTTT | 10043 |
rs140480886 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35329207 | GTGATCCACCCGCCT[C/T]GGCCTCCCCAAGTGC | 10043 |
rs140565759 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime, nc-transcript-variant, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299876 | ACGGGTCGGTGGCGC[A/T]GGCGGTTGCTGTCAG | 10043 |
rs140576566 | snp | A/G | 0.000261956 | 0.0114416 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323882 | CCGCCCATACTCTCC[A/G]GTGACACGCCCATAG | 10043 |
rs140584600 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35333677 | GGTCACTGCCCCTGG[A/C]AGCCCCACAAGTCCT | 10043 |
rs140691385 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35346817 | GGCGTGCAGAGCCTG[A/G]GCTGGGACCCAGTGC | 10043 |
rs140915364 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35313040 | TCCCAGAAGGCTGGT[C/G]TGGAAAGGGGTGATA | 10043 |
rs141063632 | in-del | -/GTGGA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305903 | TCCTGTGTTGGTTAG[-/GTGGA]CAGACTAGACCAGGG | 10043 |
rs141207336 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | TOM1 | GRCh38.p7 | 22:35304933 | AGTCCCTGGGGATGA[G/T]CCTCAGTGGTTGGGG | 10043 |
rs141309947 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35325058 | CATGACCAGCTCGTA[G/T]AGCTGGGGGCTTGTC | 10043 |
rs141352986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35309402 | TAATCCCAGCACTTT[A/G]GGAGGCCAAGACAGG | 10043 |
rs141356796 | in-del | -/CAC | 0.497641 | 0.0342639 | intron-variant | TOM1 | GRCh38.p7 | 22:35342964 | ACACACCCCTACACA[-/CAC]CACACCTACACACTC | 10043 |
rs141413174 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TOM1 | GRCh38.p7 | 22:35321560 | CATACCACCACGCCC[A/G]GCAAATTTTTGTATT | 10043 |
rs141518158 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35326668 | GAGGGTGGAATCCCA[A/G]TCCTCTAGGAGGAGA | 10043 |
rs141564914 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35345042 | GCCCCTGCAGAAGCC[A/G]TTAGAGAGGAAAGCC | 10043 |
rs141657580 | snp | C/T | 0.000307953 | 0.0124049 | missense, nc-transcript-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334363 | AGAGCTGGCCTGCAG[C/T]CTCTGGAGGCCTCTG | 10043 |
rs141665203 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35302074 | TTCTTACCTTGAAGC[A/G]TTGCCTTTCTTGGGC | 10043 |
rs141753674 | snp | A/G | 0.000365442 | 0.0135125 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35333424 | AAGTGAGGCCGAGCC[A/G]GCAGCTGACCTGATC | 10043 |
rs141830410 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | TOM1 | GRCh38.p7 | 22:35303864 | GTTAGTGGTTGTGCA[C/T]GTCTGTCTCCACAGC | 10043 |
rs141869389 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35301257 | ATACACACACACACA[A/C]GCACACATATATATA | 10043 |
rs141869717 | snp | G/T | 0.00517822 | 0.0506191 | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347268 | ACACCCTTAGGCTGG[G/T]ACCTCCCTCCCTCCT | 10043 |
rs141876982 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35340782 | GAGGGACGAGTTGTG[A/G]AAACCGTCCAGGCCA | 10043 |
rs141963980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35331985 | AATGAGGCTTGTGGC[A/G]TAAGTGAGAGTCCAT | 10043 |
rs142063849 | in-del | -/AC | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343300 | TACACACACAGCCCT[-/AC]TACACACCACACCTA | 10043 |
rs142184026 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35303361 | TCCGCTTCCTCCTTG[A/G]TAGAATGTTACTAAC | 10043 |
rs142241695 | snp | A/G | 0.000247368 | 0.0111186 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323522 | CGCGTTCCGCAGCTC[A/G]CCCGATCTGACAGGT | 10043 |
rs142363695 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35306354 | GTGCTTATCCCCACA[A/G]TGTGCCCATGTGAGC | 10043 |
rs142456405 | snp | A/C/T | 1.78576e-05 | 0.00298806 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323905 | GCCCATAGCACCAAC[A/C/T]CCGGAACAGGTAAAC | 10043 |
rs142462711 | snp | C/G/T | 6.87042e-05 | 0.00586072 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323867 | GCCCCTCTGCCCGCC[C/G/T]CGCCCATACTCTCCG | 10043 |
rs142487449 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35323300 | CATTTCGGGGCGTCT[C/T]GGTTGTCGGCTGGTG | 10043 |
rs142548408 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | TOM1 | GRCh38.p7 | 22:35345346 | TGACCCTGGGCTTGG[C/T]GTGTCTTTTGTCAGA | 10043 |
rs142594671 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TOM1 | GRCh38.p7 | 22:35328808 | GAAAGGCGTGCTGGC[A/G]TGAGGCCACAGTCGG | 10043 |
rs142610034 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35342857 | CCACACCTACACACT[C/G]ATGCACCTACACACA | 10043 |
rs142648744 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337884 | AGGGCTCTTTCCCTG[C/T]AACAGGGCTGGGTCC | 10043 |
rs142753294 | snp | A/G | 0.00127959 | 0.0252618 | intron-variant, nc-transcript-variant | TOM1, MIR3909 | GRCh38.p7 | 22:35335653 | GAGGTATGCTGTTGC[A/G]CTGTCCTTCCTCTGG | 10043 |
rs142800352 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35326178 | GCTGCTGTCACAATC[A/G]TGAATGTATATAGTG | 10043 |
rs142882370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35346331 | CGCAGCATCTGCCAC[C/T]CCGTCTCTGGGCACC | 10043 |
rs142943654 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35314553 | CTTACTTGCCTTTCC[-/A]AAAACAACCACAGCC | 10043 |
rs143069756 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348391 | CACAGCCTGGGGCTA[C/T]GCACTGGCTCGTAGC | 10043 |
rs143199209 | snp | A/G/T | 6.6018e-05 | 0.00574504 | synonymous-codon, intron-variant, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323510 | GTCCTGGGCTGACGC[A/G/T]TTCCGCAGCTCGCCC | 10043 |
rs143262889 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TOM1 | GRCh38.p7 | 22:35300341 | CTCTGCTGGGTCCCG[C/T]CGCCTGGGCTCTGGC | 10043 |
rs143281269 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35321083 | AGCTGGGCTCAGGGA[C/G]TCATGCCTGTAATCA | 10043 |
rs143287048 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35317180 | CCAACTCAAAAGATA[A/T]TTCTTTTTTGCTTGT | 10043 |
rs143305235 | in-del | -/TAAA | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297391 | TTAAAAATAAATAAA[-/TAAA]TAAATCCATATACTT | 10043 |
rs143595470 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35313581 | TTACGGGTGCAAAAA[C/T]AGAGACTCAGAGGGG | 10043 |
rs143641128 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35325666 | TGAGTGGGTTAAAGG[A/T]GTGTAAAAAATTGTA | 10043 |
rs143666260 | snp | A/G/T | 0.00637159 | 0.0561118 | intron-variant | TOM1 | GRCh38.p7 | 22:35309568 | AGAATCGCTTGAACC[A/G/T]GTGAGGCGGAAGTTG | 10043 |
rs143680802 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337584 | CTTCAAAATGACTGC[A/G]TGGGAACTGGGGGTC | 10043 |
rs143787338 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35344233 | GAAAAGCCTCAGTGA[C/G]TGGATGGTGAGACAA | 10043 |
rs143858975 | snp | A/C | 0.00755907 | 0.0610114 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297347 | AGTTGTACCACTGTA[A/C]GCCAGCCTGGGTGAC | 10043 |
rs143894620 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35319410 | CCTAAACTTAGCCTC[A/G]TTGCTAAAGTGTCTC | 10043 |
rs143914951 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35314747 | CTTCTGGGAAAACAG[C/T]GTTCCCCGCCCCTGC | 10043 |
rs143977846 | snp | C/G/T | 0.000563266 | 0.0167732 | synonymous-codon, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323126 | GAGGACCATCCTGCC[C/G/T]AAGAACAACCCACCC | 10043 |
rs144090892 | snp | G/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298820 | CATCACAATAAGTAC[G/T]TAAGCACCCACAGTA | 10043 |
rs144111179 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35341292 | CACACTACGGTATTA[C/T]GGCACTTACGCTTCG | 10043 |
rs144192361 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35332531 | CCCCTAAGTAGCTCC[A/G]TAAAACAAGATTAGA | 10043 |
rs144221305 | in-del | -/CA | 0.449473 | 0.150701 | intron-variant | TOM1 | GRCh38.p7 | 22:35343343 | CCCCCACACACACAC[-/CA]CCACACACATCTACA | 10043 |
rs144230385 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35328070 | CTTCGTGTAACTGTT[C/T]GAGTTCCTACTGCTC | 10043 |
rs144237182 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | TOM1 | GRCh38.p7 | 22:35310498 | GTTGGAGGTTGCAGT[A/G]AGCCGAGATCGTGCC | 10043 |
rs144359449 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35316385 | TTGACGCGTGAAGAT[A/G]GCATCTAGGAAGGCG | 10043 |
rs144430799 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35311740 | TCTAGCAAGTCACAA[A/T]CCTCTGCACATTGGC | 10043 |
rs144462322 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | TOM1 | GRCh38.p7 | 22:35302600 | GCCTCCCAAAGTACT[G/T]GGATTACAGGCATGA | 10043 |
rs144533993 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305910 | GTTGGTTAGCAGACT[A/G]GACCAGGGTCAGTGA | 10043 |
rs144565800 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35313240 | TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 10043 |
rs144626971 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35308654 | TCCAGATTGTCAGCA[A/G]TACCTTTTACACTCC | 10043 |
rs144666866 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | TOM1 | GRCh38.p7 | 22:35346842 | CAGTGCTGAGGTTCA[G/T]CGGGGCCCGAGCTGC | 10043 |
rs144721465 | snp | C/G/T | 0.000249308 | 0.0111621 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347112 | GATTGCCCAACCTCT[C/G/T]CAGCCCCTCAGCTGA | 10043 |
rs144770064 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35331529 | TGATGGCAGCCCCAC[C/T]GGGATGATGTGAAAT | 10043 |
rs144828252 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35315948 | TAGCCGTGTAGCAAG[C/T]GAAGAGTCACCCACC | 10043 |
rs144857848 | snp | C/T | 0.000153988 | 0.00877328 | stop-gained, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35345764 | ATGGAGGACATCGAG[C/T]AGTGGCTGTCCACTG | 10043 |
rs144941798 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35333621 | GGACCCCACCTTGCT[A/G]GGGTCCCAGGCTGAA | 10043 |
rs145024189 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | TOM1 | GRCh38.p7 | 22:35330287 | GTCTCACAAAAAAAA[A/G]AAGAGACGGCCTCAC | 10043 |
rs145084012 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35318265 | CTAGGATGAGGCAAG[A/C]TGGAGACTCTTAATC | 10043 |
rs145128822 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35332810 | CACTGCTAGTTACCC[A/G]GGGACAGCAGGCATG | 10043 |
rs145159534 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35300194 | GATAGATGTATATGA[C/T]AGCCAGTAGGTAAGG | 10043 |
rs145190229 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305061 | CACAAAAGCCAAGCC[A/G]GGGGAGCCACAGGAA | 10043 |
rs145195807 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35342694 | CCTCATCCCTCTACA[C/G]CAGCCGCCACATCCA | 10043 |
rs145343754 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | TOM1 | GRCh38.p7 | 22:35309932 | GAAGTCCCAGGGCTA[C/T]TTCTGGCTGCAAGGG | 10043 |
rs145363094 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35307709 | GAGTCTTCCCAGAAG[A/G]GAAGGACGGAGCCAG | 10043 |
rs145365864 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348319 | GTGTGGACTGTGTGC[A/G]CATGTGGGGTGCACA | 10043 |
rs145376314 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35307322 | CATGGCTTTGATGTT[C/T]GTGTTTTTTTCCTAT | 10043 |
rs145512529 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOM1 | GRCh38.p7 | 22:35322384 | AGTTGGGTGCTGCTC[A/G]GCACTTTGGTGCTCT | 10043 |
rs145658731 | in-del | -/AC | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343454 | CCACCACACACACCT[-/AC]ACACACACATTCATA | 10043 |
rs145683282 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35329313 | TTAAAAGTCGGTGAC[A/G]TGATAACTAAATGCA | 10043 |
rs145778235 | snp | A/G | 0.00953873 | 0.0683987 | | | GRCh38.p7 | 22:35337462 | CTGCCGTAGTCACTG[A/G]CCCACTTGCCATGGA | 10043 |
rs145795818 | in-del | -/GGGGGGGG | | | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35299918 | GTTGGTGGCAGCGGC[-/GGGGGGGG]GGTAGCAGCAATGGA | 10043 |
rs145908532 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35318922 | TTTGCGTGGAGAGGC[A/G]CAGGCTGGATGCAGG | 10043 |
rs145991196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35302771 | CCCCAGTAAATTGAC[A/G]GCAAAACTGAGTCAT | 10043 |
rs146147301 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35326189 | AATCATGAATGTATA[C/T]AGTGACACTCTGAAA | 10043 |
rs146200939 | snp | C/T | 0.00350717 | 0.0417287 | missense, nc-transcript-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334433 | GGGGCAGCTCACTGG[C/T]TGACCAACGGAAAGA | 10043 |
rs146232102 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35340906 | GGGCAAGGTGGAGGA[C/T]GCTGGGGTGGGCCAT | 10043 |
rs146265520 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35345088 | TGTGTGGGAGCCATC[A/G]TGGCACAGCCCATGT | 10043 |
rs146324937 | snp | A/G | 0.00175824 | 0.0295978 | intron-variant, synonymous-codon, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35299952 | TCTCCTGGGGAACCC[A/G]TTCAGCTCTCCAGTG | 10043 |
rs146476454 | snp | C/T | 0.000107352 | 0.0073256 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323907 | CCATAGCACCAACCC[C/T]GGAACAGGTAAACGA | 10043 |
rs146488189 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298984 | TAGAATCACAACGCT[A/G]GGAAAGGCCTTTGAG | 10043 |
rs146574870 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | TOM1 | GRCh38.p7 | 22:35333316 | GGTGACAGATCCCTG[C/G]GCAAAGCCTGCAAGC | 10043 |
rs146608045 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35316622 | CAGAACTCTGCAGCC[A/G]ACTCCCGGCCTGGAA | 10043 |
rs146664922 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338264 | GTGCAAGACAAGATG[A/G]CACCTCACCCAGCAG | 10043 |
rs146672758 | snp | C/T | 0.000153988 | 0.00877328 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323521 | ACGCGTTCCGCAGCT[C/T]GCCCGATCTGACAGG | 10043 |
rs146727337 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337180 | TGACCTCGTGATCCG[C/T]GCGCCTTGGCCTCCC | 10043 |
rs146851130 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334993 | TCTGTCAGCCTTGCC[C/T]CAGAGCTGGGGCTCT | 10043 |
rs147007723 | snp | G/T | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297827 | GTTGTCTCTGTTTTT[G/T]TTTTTTTTTGTTTTT | 10043 |
rs147076822 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TOM1 | GRCh38.p7 | 22:35301713 | GAGGTTTTGTAATCA[A/G]TGCTCTCCAAGGGGG | 10043 |
rs147118957 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | TOM1 | GRCh38.p7 | 22:35303937 | CAGACCCTCAGCACC[C/T]AGCACGGTGCCTGGC | 10043 |
rs147130709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35327988 | TGGAGGCCAGTCATA[A/G]AGGCACCAAGAGAGC | 10043 |
rs147202629 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | TOM1 | GRCh38.p7 | 22:35314363 | AACCTCCGTCTTCTG[A/G]TTGGCTCTGCCCACT | 10043 |
rs147343415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TOM1, MIR6069 | GRCh38.p7 | 22:35336307 | TAAATGCTTCTGGTG[C/G]ATCTTCCAGCTCTGG | 10043 |
rs147478505 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35309575 | CTTGAACCGGTGAGG[C/T]GGAAGTTGCAGTGAG | 10043 |
rs147639234 | in-del | -/TG | | | intron-variant | TOM1 | GRCh38.p7 | 22:35308215 | GCTCGCTCTTTCTCC[-/TG]TGTGTGTGTGTGTGT | 10043 |
rs147700563 | snp | A/T | 0.000193133 | 0.00982493 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323888 | ATACTCTCCGGTGAC[A/T]CGCCCATAGCACCAA | 10043 |
rs147723349 | snp | C/T | 6.65624e-05 | 0.0057686 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35346965 | TAAGGGGGTCACCAG[C/T]GAAGGTAGTAGTCCC | 10043 |
rs147743896 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35307410 | CTTTAAGTTTGCCCA[G/T]GAGCCCACCTGGCAT | 10043 |
rs147754742 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | TOM1 | GRCh38.p7 | 22:35304419 | CCCTCTTCTTTCAAG[A/G]ATTTCAAACCCTTTC | 10043 |
rs147838276 | in-del | -/G | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297837 | TTTTTGTTTTTTTTT[-/G]TTTTTTTTTTTTTTT | 10043 |
rs147849137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35328260 | CCCAGTAAGGGCTCC[A/G]AAAGAGAGAAGACTG | 10043 |
rs147859095 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35324670 | TCTCCTGCCTCAGCC[C/T]CCTGAGTAGCTGGGA | 10043 |
rs147868308 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35306473 | TTGTCTAGAAAGGGC[A/T]TTGTATCAGCTGTAC | 10043 |
rs147954388 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35300364 | GCTCTGGCCAGCTCC[A/T]TCCTGGCTCACCGGG | 10043 |
rs147954716 | snp | C/T | 0.00161093 | 0.028335 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35346940 | CCCAGGGTAATGATG[C/T]GGAAGAGCCTAAGGG | 10043 |
rs148068600 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35314180 | TGGAGGAACCTGGAG[A/G]AACCTAGAAGGGGTT | 10043 |
rs148262357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35309338 | ACTTTTCCATCTCAC[C/T]GATTCCCCCTTAGAA | 10043 |
rs148331922 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TOM1 | GRCh38.p7 | 22:35321406 | TCGCCCAGGCTGGAG[C/T]ACAGTGGCGCAATCT | 10043 |
rs148345194 | in-del | -/C | 0.0162398 | 0.0886349 | intron-variant | TOM1 | GRCh38.p7 | 22:35319234 | CTTGGGGACAGCAAG[-/C]CCCCCATGTCCCTTA | 10043 |
rs148398848 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35336847 | AAGTGCTTGGCCCTC[C/T]ACCACCACAGGCATG | 10043 |
rs148440565 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35322437 | ACCAGTGGCTGAGAA[C/T]AGTCTTGCCCACACC | 10043 |
rs148440676 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305908 | GTGTTGGTTAGCAGA[C/G]TAGACCAGGGTCAGT | 10043 |
rs148521739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35345978 | AAGTCCTGGGCACAG[C/T]AGCCTCTCGGCTGCT | 10043 |
rs148616315 | snp | A/G | 0.0023933 | 0.0345097 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297424 | TCCATTTCTGTTTCA[A/G]TAGCTATATAGTAAT | 10043 |
rs148679020 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | TOM1 | GRCh38.p7 | 22:35340668 | GGGAGGATCGCTTGA[G/T]CACAGGAGGTGGAGG | 10043 |
rs148784154 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35310537 | CCAGCCTGGGCAACA[C/G]TGAGACTCTGTCTCA | 10043 |
rs148842882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35307669 | CTCCTGCTGGGGAAG[A/G]TAGAGAAGGGAAGGA | 10043 |
rs148894578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35313506 | TTTCCTGATGTCATA[C/T]TGACATTGTCTGGCT | 10043 |
rs148913558 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35328277 | AAGAGAGAAGACTGC[A/G]CAGGCAGCCTCGCAC | 10043 |
rs148922877 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337562 | GGAAGGAACAGACAG[A/C]AGCACTCTTCAAAAT | 10043 |
rs149050941 | snp | C/T | 0.00993419 | 0.0697739 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348358 | GAGGATGCTGGCCTT[C/T]CGAGGCTGGGTGCCA | 10043 |
rs149055276 | in-del | -/GGG | | | cds-indel, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35345771 | CATCGAGCAGTGGCT[-/GGG]GTCCACTGACGTGGT | 10043 |
rs149137970 | in-del | -/AC | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301244 | GAAACACATACACAT[-/AC]ACACACACACACGCA | 10043 |
rs149378158 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35325517 | TTGGAGACAAGTTCT[C/G]TTTAGAAATAACTCC | 10043 |
rs149431001 | snp | C/T | 0.000667482 | 0.0182564 | intron-variant | TOM1 | GRCh38.p7 | 22:35331378 | TGGCCTCCGAAAGCA[C/T]TGGTATTACAGGCAT | 10043 |
rs149455664 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | TOM1 | GRCh38.p7 | 22:35340434 | TGACTTCCAATCTGA[A/C]AGATCAGGATGGAGC | 10043 |
rs149508752 | snp | A/G | 0.000116195 | 0.00762129 | missense, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323055 | TGTGTCAAGAACTGC[A/G]GGCACCGCTTCCACG | 10043 |
rs149594558 | in-del | -/AATA | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297385 | CTGTCTTTAAAAATA[-/AATA]AATAAATAAATCCAT | 10043 |
rs149780801 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35315718 | AAGTTGGGCCAATTG[A/C]AAAACCAAGGTCTCA | 10043 |
rs149833008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35322343 | TAAACCCAGGCCTCC[A/G]CGGGGGCAGGGAGGC | 10043 |
rs149877665 | snp | A/G | 0.00081833 | 0.0202113 | missense, nc-transcript-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338786 | CAGCAGAGCACTGGC[A/G]CGGTAAGCAGAGGGG | 10043 |
rs149909828 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35327869 | GCAGGTGGAGCTAGT[G/T]GTTCCTGCTCCCGGG | 10043 |
rs149961641 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TOM1 | GRCh38.p7 | 22:35332714 | AACCTATTCCTGTTT[A/G]TTTGTTTCATGCTAC | 10043 |
rs149972642 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | TOM1 | GRCh38.p7 | 22:35342083 | GAGTTTGAGGTTATC[A/G]TGAGCTATGACTGTA | 10043 |
rs150015044 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35300148 | ACTCTTGATTGACAA[A/G]AACTTGGGCCATTAG | 10043 |
rs150081207 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35344655 | TGCCTGGGGGGTCCT[C/G]AGGTGCTGGGTGACA | 10043 |
rs150099498 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35342354 | CCAGCCAGGCACAGG[A/G]TGACGGGCTGGGAGC | 10043 |
rs150110673 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TOM1 | GRCh38.p7 | 22:35302306 | AATGTGAATTTCTTT[C/T]TTTTTCTTTTTCTTT | 10043 |
rs150310295 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35317794 | TCTCATCCGGCCCTG[C/T]ACCCCCCTCCTCTCC | 10043 |
rs150318119 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35340136 | ATTTCTGCTCCAGCA[A/G]GTGAGCAGACAGAGC | 10043 |
rs150362231 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TOM1 | GRCh38.p7 | 22:35325285 | CACTGCCCACTTTTT[A/G]TATCATTTGAACTCA | 10043 |
rs150451594 | snp | C/T | 3.50982e-05 | 0.00418902 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323887 | CATACTCTCCGGTGA[C/T]ACGCCCATAGCACCA | 10043 |
rs150478150 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334029 | TGAAAAAATCGACTA[C/G]CCATCTGATTACTGT | 10043 |
rs150533423 | in-del | -/C | 0.0217236 | 0.101931 | intron-variant | TOM1 | GRCh38.p7 | 22:35328661 | GGATGTTGAAAGGCA[-/C]CCGCCCTGTCCCCGT | 10043 |
rs150557053 | snp | A/C | 1.66098e-05 | 0.00288177 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35333427 | TGAGGCCGAGCCGGC[A/C]GCTGACCTGATCGAC | 10043 |
rs150588657 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337037 | ACCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTC | 10043 |
rs150650112 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35346360 | CCAAGGCCCACATGG[A/G]CACTTCAGGCCCAGA | 10043 |
rs150764523 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35309476 | TGGTAAAACCCCATC[C/T]TTACTAAAAATACAA | 10043 |
rs150786456 | snp | A/G | 0.000395329 | 0.0140538 | missense, nc-transcript-variant, intron-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35321964 | TCCTCCTTAGTCCCA[A/G]AGATGCCCTCCGAGC | 10043 |
rs150835260 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35321685 | ATTACAGGCATGAGC[C/T]ACCGCGCCCGGCCAG | 10043 |
rs150979960 | in-del | -/TATATAT | 0.0573587 | 0.15934 | intron-variant | TOM1 | GRCh38.p7 | 22:35301313 | ATACATACACATACA[-/TATATAT]TATATGTATTTACAC | 10043 |
rs150989749 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | TOM1 | GRCh38.p7 | 22:35328978 | TTATTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT | 10043 |
rs151113735 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337704 | TTCCTGAAGCCTACA[A/G]TTAGACCAGCCCCGC | 10043 |
rs151225253 | in-del | -/CA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343160 | CACCACACACACCTC[-/CA]CACACCACACCTACA | 10043 |
rs151273039 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35341399 | CTCGTAGGTATTGTT[A/C]TGCCTGGCTTCTAAG | 10043 |
rs151275570 | in-del | -/ACACACAC/ACACACACAC | 0.483418 | 0.0895317 | intron-variant | TOM1 | GRCh38.p7 | 22:35303131 | CCACCTCCCCTCCCA[-/ACACACAC/ACACACACAC]ACACACACACACACA | 10043 |
rs151291104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35311287 | TCCTTAAAGAGGAAT[A/G]TTAATCACGAATACT | 10043 |
rs151314362 | snp | C/G | 0.000153988 | 0.00877328 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323876 | CCCGCCCCGCCCATA[C/G]TCTCCGGTGACACGC | 10043 |
rs180694031 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35308958 | CTCAGCAAATTAGGA[G/T]ATGGATGGAACTTTC | 10043 |
rs180698298 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35300324 | TGGCAGTGGCTGGGC[A/C]ACTCTGCTGGGTCCC | 10043 |
rs180702624 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35328308 | GCCCCAAGCCAAGGC[C/T]ATGAGATGTGAGCAG | 10043 |
rs180709913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35317796 | TCATCCGGCCCTGCA[C/T]CCCCCTCCTCTCCCA | 10043 |
rs180715835 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35342625 | CAGCCTACCCAGGGC[A/G]CTGGCATCCCAGAGC | 10043 |
rs181007502 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35313261 | CTGAGGCAGGAGAAT[C/T]GCTTAAACCCGGGAG | 10043 |
rs181052893 | snp | C/T | 0.00222337 | 0.0332677 | intron-variant | TOM1 | GRCh38.p7 | 22:35323732 | GGCTCTTGATGTTCC[C/T]AGGAGCCCTCACTGA | 10043 |
rs181063196 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35304730 | TGAACCACCCACCTC[A/G]GCCTCCCAAAGTGCT | 10043 |
rs181178796 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35309878 | CAAAACCTTCCCCAG[C/G]AGCCGCCCAAGAGAC | 10043 |
rs181178978 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35328979 | TATTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTC | 10043 |
rs181346222 | snp | A/G/T | 0.00438524 | 0.0466503 | utr-variant-5-prime, upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299309 | GCTAGAGGGAATTGC[A/G/T]CTGCAATTCATTAAA | 10043 |
rs181358691 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TOM1 | GRCh38.p7 | 22:35339898 | GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA | 10043 |
rs181372044 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35303275 | TTGCCCCAAGCCCGA[C/T]GTTGCTCTTTTACTC | 10043 |
rs181473064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35316878 | GATACCTTACTGTGC[C/T]GGTACCTTGCATGAA | 10043 |
rs181501528 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35313905 | GCACAGCTGCTACCC[A/G]GAGGCCCTTGAAGGT | 10043 |
rs181638000 | snp | A/G | | | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334820 | CTGGTTCCAAAACAC[A/G]GTGTCTCCACCCCCC | 10043 |
rs181673583 | snp | A/G | 9.14369e-05 | 0.00676093 | intron-variant | TOM1 | GRCh38.p7 | 22:35300017 | CAGCTCCGCCCCGGT[A/G]CTCCGCACCCAGCTT | 10043 |
rs181885288 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | TOM1 | GRCh38.p7 | 22:35317353 | TGCCACCATGCCCAG[C/G]TACTTTTTTGTAGTT | 10043 |
rs181955155 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35303616 | GATTCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG | 10043 |
rs181956635 | snp | C/T | 6.72495e-05 | 0.0057983 | intron-variant, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323017 | CTCGACGGCACCTCT[C/T]GGCCCTCCAGGTCTT | 10043 |
rs182016098 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335599 | CACTGCTGGCCATAC[C/T]GGAGAACCCTGGCGC | 10043 |
rs182163646 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | TOM1 | GRCh38.p7 | 22:35341229 | CTGAGTTCCAGGAAG[A/C]GCTTAAGTGAAACCA | 10043 |
rs182167268 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347803 | ATCAGCCCCAGGCTG[C/T]AGGTGAGGCTTCAGG | 10043 |
rs182205396 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant, downstream-variant-500B | TOM1, MIR6069 | GRCh38.p7 | 22:35336574 | CAGCAGAGACGCCTC[A/G]GCTAGGCCTTCACAA | 10043 |
rs182301203 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35314579 | CAGCCTCTCCTGAAA[C/G]ACTGATGTTCCCTCC | 10043 |
rs182356023 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35315132 | ATGGGTGGGAGGAGG[A/G]AGGCAGGAGGAGGGA | 10043 |
rs182423334 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35311130 | ATCAGCTGAGCTGGT[A/G]AGTGGGAGTGGGAGG | 10043 |
rs182478828 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35311589 | TCATTCCAAAAGTAT[C/G]TAATGCCCCCCTCTG | 10043 |
rs182481836 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35332091 | CCCTTGTTCATTTTT[C/T]GTGTCTTTCTCCATC | 10043 |
rs182588452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35326188 | CAATCATGAATGTAT[A/G]TAGTGACACTCTGAA | 10043 |
rs182684346 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | TOM1 | GRCh38.p7 | 22:35330792 | GCCTGGTGTGTCCTC[A/G]CCCACTCCACCACTT | 10043 |
rs182861356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35307980 | CAGACCCGCGTAAAG[C/T]GTATTGCCCTCAATA | 10043 |
rs182899660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35301265 | ACACACACGCACACA[C/T]ATATATAAAAATATA | 10043 |
rs182910201 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35324731 | TTTTTTGTATTTTTA[C/G]TAGAGATGGAGTTTC | 10043 |
rs183040726 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35320162 | TTCTTCTCTACCCAG[A/G]GTGGGCCCCCAGTTC | 10043 |
rs183199199 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35319275 | AGGAACAGGCTCGGC[A/G]TCGGTCAGGTGCATT | 10043 |
rs183200367 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35329494 | GGTCAAGGGTATATG[C/G]GAACTTGTGGTACTA | 10043 |
rs183206376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35301733 | CTCCAAGGGGGAGGT[A/G]GCAGTCCAGGATTTA | 10043 |
rs183305524 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35315673 | GGCCACCCTGGCATC[C/T]GTCTGGCTCAGGACC | 10043 |
rs183315547 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35325923 | ATTTGGATACATGGG[A/G]TTTGTGATCAGTAGT | 10043 |
rs183423302 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343098 | ACCACACCTACACAC[A/C]CATACACCACACACA | 10043 |
rs183553474 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337351 | GCAACAAGCACCTCC[A/G]GACCCTCAATTAGCA | 10043 |
rs183679215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35302657 | TTTCTGTTGAGTTCC[C/T]GGGTAATGCTAATGC | 10043 |
rs183679312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35320368 | ATACCTGTATAGGGC[C/T]GAGGGTGGAGGATGG | 10043 |
rs183695432 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | TOM1 | GRCh38.p7 | 22:35346625 | GGTGCTGGGCTTGGC[A/G]TGCTGTGTGTTATCC | 10043 |
rs183790116 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298164 | AAATGGCCTTCTCCC[C/T]GCTTATACTCCAAAT | 10043 |
rs183799066 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35306763 | ACCCAGTCTAAGTTA[A/G]TAGCCAAGCTAAGTG | 10043 |
rs183826938 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35316547 | AAGGCTGCCAAGCCC[A/G]GTGCTTGCTACCATG | 10043 |
rs183834784 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35339616 | GAGGAATAAAAGAGC[A/G]GACCCTGGCCAGGCG | 10043 |
rs183836169 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35310391 | AACCCTGTCTCTACT[A/G]AAAATACAAAAATTA | 10043 |
rs184150651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35313549 | CATCCTGTGAGGCAG[A/G]CAGTCTTATCCTGAT | 10043 |
rs184158492 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334717 | GTCTGATCAGAGGGG[A/G]AAACTGAGGCACAGA | 10043 |
rs184242970 | snp | C/T | 0.0263992 | 0.111815 | intron-variant | TOM1 | GRCh38.p7 | 22:35308217 | TCGCTCTTTCTCCTG[C/T]GTGTGTGTGTGTGTC | 10043 |
rs184249243 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35326938 | TGCAGCGTCCCTCCC[C/T]GCCTTGTGGGGAGCC | 10043 |
rs184367687 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TOM1 | GRCh38.p7 | 22:35303379 | GAATGTTACTAACAG[C/T]ATCTGCCTCACAGGG | 10043 |
rs184377593 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | TOM1 | GRCh38.p7 | 22:35322478 | CCCAGATCTCAGGGC[A/G]GCCAGACACACGTGG | 10043 |
rs184698452 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35303150 | CACACACACACACAC[A/C]CCTTTGTGCTTGCTG | 10043 |
rs184728690 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348437 | GAGAAGCAAAGTGAG[C/T]GTCCTCGATGTATAG | 10043 |
rs184871110 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35316023 | AGGACAGCGTGACAT[C/T]ACGTGGAATAACAAG | 10043 |
rs184884915 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35317048 | GATTCTAGAGGAACC[G/T]GGTTACAGGGGATGC | 10043 |
rs185005448 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35340157 | CAGACAGAGCAGGTC[A/C]CATGGGAGACAGTTA | 10043 |
rs185145659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35318198 | CGCCTCTCTTAGTGG[C/T]AGCCCAGATTCCACA | 10043 |
rs185154559 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35344081 | CCCCTACACACACAC[A/G]CCTCCCAAAGTGGCA | 10043 |
rs185200942 | snp | C/T | | | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35333909 | GTAGTTGGCCATTGT[C/T]ACTGTTATCACTGTG | 10043 |
rs185310508 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35312209 | AGATCGCACCACTGT[A/G]CTCCAGCCTGGGCGA | 10043 |
rs185517948 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338673 | TTGCATCAGCCATCG[A/C/G]TAAGGGCAGCATCCA | 10043 |
rs185520044 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35308504 | GGCCAGGCTGGTCTT[G/T]AACTCCTGACCTCGT | 10043 |
rs185657566 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35312708 | AGATGAGCATGTGAA[C/T]TGGATGAGCCTGACT | 10043 |
rs185667346 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35327502 | CATACTCCTTGGTCA[C/T]AGTTGGGGACATGTT | 10043 |
rs185777886 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301007 | GCTTGAGCCCAGGAG[C/T]TCGAGACCAGCCTGG | 10043 |
rs185792623 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334110 | GTTCTCTAACGCTCA[C/T]AGCAGCCCCAAGAGG | 10043 |
rs185826444 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35310263 | GACGTGGTACTTTTT[A/T]AAAGTATTCAAAGGG | 10043 |
rs185830547 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35328993 | CGGAGTCTTGCTCTG[C/T]CACCCAGGCTGGAGT | 10043 |
rs186013572 | snp | A/C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35328620 | CCACCGTGTGCTTGG[A/C/T]CATAAGAGCAGGAGG | 10043 |
rs186021660 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35300495 | AGCGCCGGACAGCCC[G/T]CGGCCAGGCCTCACA | 10043 |
rs186063073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35341285 | CCTGGCACACACTAC[A/G]GTATTACGGCACTTA | 10043 |
rs186130910 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35309100 | TGCTTGAAATTCTCA[A/G]TCATGTTGTGGTTGA | 10043 |
rs186173614 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35305967 | AAATACTTGTGGCTT[C/T]GTGAACCAGATGGTC | 10043 |
rs186178089 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35324851 | CACCACACCCAGCCA[A/G]GAAGGTTTGAGGCTT | 10043 |
rs186240995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35300191 | TGTGATAGATGTATA[C/T]GACAGCCAGTAGGTA | 10043 |
rs186244947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35317524 | AGGGAGAACATCTTA[C/T]CTACAGAAATGAAGC | 10043 |
rs186344694 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TOM1 | GRCh38.p7 | 22:35304753 | AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACTG | 10043 |
rs186411453 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35314680 | CACTGAGAGGCCTGC[C/T]GGTGGAGCTCAGGGA | 10043 |
rs186726667 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35311295 | GAGGAATATTAATCA[C/T]GAATACTTTGAGCTG | 10043 |
rs186821029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335124 | CGGGAGAACTGGCCC[C/T]GTACAGGCTTGTAAG | 10043 |
rs186845291 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35315393 | ACATGACTAACCCCC[A/G]CCCCAAAACCCTCCA | 10043 |
rs186852853 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337082 | CTGGGGACTACAGGC[A/G]CCCACCACCACACCT | 10043 |
rs186881471 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35329081 | CTGCCTCAGCCTTCC[A/T]AGCAGCTGGGATTAT | 10043 |
rs186990450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35310954 | GGAATAGGCCCTGGC[A/G]GGGTGGGGGGTGTCA | 10043 |
rs187024307 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35313908 | CAGCTGCTACCCGGA[A/G]GCCCTTGAAGGTTAC | 10043 |
rs187165164 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35311985 | TTCGGCTGGGCACGG[G/T]GGCTCACGCCTGTAA | 10043 |
rs187177367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35332807 | GAGCACTGCTAGTTA[C/T]CCAGGGACAGCAGGC | 10043 |
rs187202267 | snp | A/G/T | 0.000283333 | 0.0118991 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35330361 | GGAGCTCAACCGCAC[A/G/T]TGCCGAGCCATGCAG | 10043 |
rs187523436 | snp | C/T | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35302880 | TTTTAGATAAAGAGG[C/T]GGAGGAAGTACTGCT | 10043 |
rs187591679 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35303620 | CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAT | 10043 |
rs187628655 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant, downstream-variant-500B | TOM1, MIR3909 | GRCh38.p7 | 22:35335929 | TCTCAGAGGCAGGGC[A/G]GGAGAGAGGTGCCCT | 10043 |
rs187678829 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35330820 | CTTCCTGGTTCTGGG[G/T]CCTTAGACAAGTGAC | 10043 |
rs187709588 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35302436 | CGCCTCCCGGGTTCA[A/G]GCGATTCTCCTGCCT | 10043 |
rs187775822 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35320442 | CTTCCAGGGGCCTCC[C/T]AACACCGTGACCCCT | 10043 |
rs187816286 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35308002 | CCCTCAATAACATGG[A/G]TGGGCCTCGTCCAAT | 10043 |
rs188062985 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297542 | CTCACTGCAAGCTCC[A/G]CCTACCAGGTTCACG | 10043 |
rs188065104 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35316138 | GCAGGTGTGCCAAGG[C/T]CGGCAGGGTGGCTGC | 10043 |
rs188078966 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35339052 | AACTGGAGACCAGGC[C/T]GGGCGTGGTGGCTCA | 10043 |
rs188102573 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35326854 | GGAGAGAGGGCGGAA[A/T]CCCAGTCCTCTAGGA | 10043 |
rs188134866 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35319766 | GAGCCAGGGACGGGC[A/G]AGGGGCTGCCCAGGG | 10043 |
rs188219710 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35313144 | TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC | 10043 |
rs188224054 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334200 | CAGGTGGCCTGCCTC[A/G]CGCATTCCCCCACCC | 10043 |
rs188285669 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337414 | CGCCCCACCTCCCCC[A/G]CCACTGGCTTTAAGG | 10043 |
rs188402655 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | TOM1 | GRCh38.p7 | 22:35301267 | ACACACGCACACATA[A/T]ATATAAAAATATACA | 10043 |
rs188426584 | snp | G/T | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35346097 | GCATAACAGCGCCAG[G/T]CTCTTACCTGCAGTA | 10043 |
rs188546023 | snp | C/G | 0.0193772 | 0.0965046 | intron-variant | TOM1 | GRCh38.p7 | 22:35339844 | AGGAGGCGGAGCTTG[C/G]AGTGAGCCGAGATCC | 10043 |
rs188549780 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35309106 | AAATTCTCAATCATG[C/T]TGTGGTTGATATGTT | 10043 |
rs188564503 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35328858 | GGACCTCAGGACCCA[A/G]GCACCTGCCGTGACC | 10043 |
rs188688727 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | TOM1 | GRCh38.p7 | 22:35313551 | TCCTGTGAGGCAGGC[A/G]GTCTTATCCTGATTT | 10043 |
rs188690755 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334771 | GGTCAAGGAGCTAAT[A/G]TTTGGCAGCACTAGG | 10043 |
rs188754395 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35315938 | GGCTTACAAATAGCC[A/G]TGTAGCAAGCGAAGA | 10043 |
rs188856679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35308345 | CTGGAGTGCAGTGGG[G/T]CAGTCTTGGCTCACT | 10043 |
rs188861323 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35326976 | AGGGCCTTGTTAGCT[A/G]CTGTGTTAGACCCAG | 10043 |
rs188909969 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334086 | GAATCAATGGATAGC[A/G]TTTTGACTGTTCTCT | 10043 |
rs188941468 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35325931 | ACATGGGGTTTGTGA[G/T]CAGTAGTTTTTCCAC | 10043 |
rs189113106 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35304037 | CAGGTATTCTGCTAG[A/C]GTCCTGGGTATTAAT | 10043 |
rs189187244 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35303513 | TTATTTCTTTTTTTT[C/T]TTTTTTTTTGAGACA | 10043 |
rs189204552 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35322611 | AAGCAAAGGCAATTC[A/C]TGCAGTGGGAAGTGG | 10043 |
rs189207999 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | TOM1 | GRCh38.p7 | 22:35307407 | TGTCTTTAAGTTTGC[C/T]CATGAGCCCACCTGG | 10043 |
rs189410945 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35323359 | AACTGCGTGCTTTGC[C/T]GTGGAGTGGGCAGGG | 10043 |
rs189432551 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35316837 | GTTTATTTTGGGCCC[A/G]TACCGTGCTGATACC | 10043 |
rs189680079 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35314712 | GAGAGGGCCAACTCC[C/T]TGTGTGGTCAGGAAG | 10043 |
rs189693319 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TOM1, MIR3909 | GRCh38.p7 | 22:35335953 | GTGCCCTGGCTCCCG[C/T]ACAGCAGCTGGGAAA | 10043 |
rs189703074 | snp | A/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35299238 | GTAAATTTATGGCAG[A/T]GACGGGTATTAAAGC | 10043 |
rs189780839 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35321459 | GCTGGAGTACAGTGG[C/T]GTAATCTCGGCTCAC | 10043 |
rs189915226 | snp | C/G/T | 0.00460224 | 0.0477487 | intron-variant | TOM1 | GRCh38.p7 | 22:35300012 | CCCCACAGCTCCGCC[C/G/T]CGGTGCTCCGCACCC | 10043 |
rs189936777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35340357 | AGCGCGGCTAGGAGC[A/G]CTGCAGATTGCATCC | 10043 |
rs190031725 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35303202 | GCTCCTGTGCCCCCA[C/T]TGAGGAGCTCCAGAT | 10043 |
rs190157274 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337269 | AATCATGGGTTTCTG[C/T]GTGTTCTGGGGCTGG | 10043 |
rs190182336 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35317091 | GGGGCTGGGGCAGGG[A/G]ACAGAGATAGATTTA | 10043 |
rs190232140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35312369 | CGACCTTTTGGAATT[A/G]TCAGTTGTGGCCTCC | 10043 |
rs190265700 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35305060 | CCACAAAAGCCAAGC[C/T]GGGGGAGCCACAGGA | 10043 |
rs190385894 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | TOM1 | GRCh38.p7 | 22:35328173 | GCTGACTCTGCAGGG[A/G]TCCTCACTTGGTGGT | 10043 |
rs190589247 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35310351 | CGAGGTCAAGAGATC[A/G]AGACCATCCTGGCCA | 10043 |
rs190602753 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35329137 | ATTTTTGTATTATTA[A/G]TAGACACAGGGTTTC | 10043 |
rs190612606 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35301440 | CCAACACCATGAGAA[C/T]CGACATGCCTTCACC | 10043 |
rs190737270 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35306015 | GTTCTGCCATTATAG[C/T]ACAAAAGCAGCTACA | 10043 |
rs190741247 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35325806 | TAAACAAAACTAATC[C/T]TTGTTTAATTCGAGA | 10043 |
rs190834819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35308529 | CCTCGTGATCCTCCC[A/G]CCTTGGCCTCTCAAA | 10043 |
rs190899761 | snp | G/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35300277 | TCCCCAATCGAGGGA[G/T]AAAGTTTTCGTGGTT | 10043 |
rs190906500 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TOM1 | GRCh38.p7 | 22:35317590 | GCACACGGAGGCCCA[C/T]CTAGATTCCCCTCTG | 10043 |
rs190916772 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35341998 | AACAGCATCAAAACC[A/T]GGCGCGGTGGCAGGT | 10043 |
rs191076624 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | TOM1 | GRCh38.p7 | 22:35318742 | CTCAGGAAAACCCAG[C/T]GAAGGCTGGGCAGAG | 10043 |
rs191134196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35344750 | CTAGTAACTAGTGCT[A/G]TTAGTGCCATTACTG | 10043 |
rs191212329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35324564 | GAAGCTTTTTTGTTT[A/G]TTCTGAAACAGTCTT | 10043 |
rs191229582 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35316481 | ATTGCGAGTTCCTGC[A/G]TTCATCATTCATGTA | 10043 |
rs191240609 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35339520 | GATATATTTAGGGAG[A/C]TTTACATGGAGTTAG | 10043 |
rs191314169 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35300881 | AACAATGCCTGGTAC[A/G]TGGCCAGTGCCATAT | 10043 |
rs191395364 | snp | A/G | 0 | 0 | intron-variant | TOM1 | GRCh38.p7 | 22:35311545 | TCAGCATCGAACTGA[A/G]CACCTAGGCAGTGCA | 10043 |
rs191399324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35331068 | ATACATCAGCTCAAA[C/T]ACTTGTCCACAAACA | 10043 |
rs191424205 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35298102 | GACCAAGCAATAAGG[C/T]TAAGTGAAGAAAGAC | 10043 |
rs191433176 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35318912 | CCGGGAGGGCTTTGC[A/G]TGGAGAGGCGCAGGC | 10043 |
rs191469704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35315477 | TTCCCAGGTGGCTCT[A/G]TAAGTGTGGAACCCC | 10043 |
rs191563858 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TOM1 | GRCh38.p7 | 22:35346492 | AGTTTGCAGTGTTAG[C/T]ATGAATGGCCCTCAG | 10043 |
rs191740832 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TOM1 | GRCh38.p7 | 22:35308155 | TCACCCTACAGATTT[C/T]CAACTTGCTAAGCCT | 10043 |
rs191756555 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35326855 | GAGAGAGGGCGGAAT[C/T]CCAGTCCTCTAGGAG | 10043 |
rs191814673 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35319874 | GTCCCTTCCACCGCA[A/G]GCCTGACCGCCTCCA | 10043 |
rs191867225 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35313972 | TTGGTAACTGGCAAC[C/G]ACTGTCCGTGTTTTT | 10043 |
rs191882249 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35333566 | CCCCTGCAGATTTTC[A/G]GGGTGCCCTTGTTAT | 10043 |
rs191895481 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35322325 | GGTGACATTGAAGCT[C/T]AGTAAACCCAGGCCT | 10043 |
rs191996137 | snp | A/G/T | 0.000117574 | 0.00766644 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35330471 | ACAATGTGTTCCTGC[A/G/T]CCATGAACGGTAGCC | 10043 |
rs192181175 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35335149 | TGTAAGAGGAACAGT[C/T]TGCTTGATGTTTTCT | 10043 |
rs192238715 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35308355 | GTGGGGCAGTCTTGG[C/T]TCACTGTAACCTCCA | 10043 |
rs192251817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35327213 | GGGTTCTGTCGCTGT[A/G]AGTAACATGGGCCCC | 10043 |
rs192303036 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35307932 | GATGTTTCTGTGAAC[A/G]TATGCCTTAGATGAG | 10043 |
rs192329857 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35311122 | TGCGGGCGATCAGCT[A/G]AGCTGGTGAGTGGGA | 10043 |
rs192461664 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35321168 | CAGCCTGGGCAACAT[A/G]GCAAGACCCCATCTC | 10043 |
rs192553892 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35302489 | TTACAGGCACGCTCC[A/G]CCACACCCGACTAAT | 10043 |
rs192566067 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35320364 | GAGTATACCTGTATA[A/G]GGCCGAGGGTGGAGG | 10043 |
rs192570709 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347625 | GGAGGCTGGCCACAG[C/T]GGAAATTCTGCCGAG | 10043 |
rs192711410 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35326142 | AATGCTTGGCACTTA[C/T]TAGGTAGTCTATAAA | 10043 |
rs192779384 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TOM1 | GRCh38.p7 | 22:35302985 | GTACCATCTCTTCTC[A/T]AGCCTGCCGACTCCC | 10043 |
rs192787549 | snp | A/G | 0.0138799 | 0.0821421 | downstream-variant-500B | TOM1 | GRCh38.p7 | 22:35348336 | ATGTGGGGTGCACAG[A/G]CCACAGGAGGATGCT | 10043 |
rs192897551 | snp | A/C/G | 0.0138799 | 0.0821421 | intron-variant | TOM1 | GRCh38.p7 | 22:35312026 | TTGGGAGGCCGAGGC[A/C/G]GGTGGATCACAAGGT | 10043 |
rs192966701 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TOM1 | GRCh38.p7 | 22:35315975 | CACCCTCCCCGAGCC[A/G]GGGCACAGCCGTGAG | 10043 |
rs193120194 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334104 | TTGACTGTTCTCTAA[C/T]GCTCACAGCAGCCCC | 10043 |
rs193188791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35337659 | GAAAGCAAGCTGGTA[C/T]TGCAAGAGTTAAATG | 10043 |
rs193271244 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35312650 | CGGGTGACTGAGGGT[A/G]TGACGTGCTTATTAG | 10043 |
rs199515324 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343736 | CACATCTACACCCAC[C/T]ACACCTACACACACA | 10043 |
rs199548413 | snp | C/T | 1.6476e-05 | 0.00287014 | intron-variant | TOM1 | GRCh38.p7 | 22:35321944 | TAAGCCCACCCTTTT[C/T]CTTGTCCTCCTTAGT | 10043 |
rs199571609 | in-del | -/ATACAA | 0.0170251 | 0.090679 | intron-variant | TOM1 | GRCh38.p7 | 22:35301284 | TATAAAAATATACAC[-/ATACAA]ACATACATATACATA | 10043 |
rs199592573 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35327211 | CTGGGTTCTGTCGCT[A/G]TGAGTAACATGGGCC | 10043 |
rs199657947 | snp | C/T | 0.000345881 | 0.0131461 | intron-variant | TOM1 | GRCh38.p7 | 22:35332960 | TCTGTCTCCATAACT[C/T]GTGTCTTTTCTGTCT | 10043 |
rs199702199 | snp | C/T | 0.000681492 | 0.0184467 | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347256 | CCCACTGCTCTCACA[C/T]CCTTAGGCTGGGACC | 10043 |
rs199705333 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347384 | TGTGGAGGCAGTGGG[C/T]TGAACTGGGGGACAG | 10043 |
rs199713787 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35308290 | CTTTTTTTTTTTTTT[C/T]CTTTTTTTTTTGAGA | 10043 |
rs199722877 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343342 | CACCCCCACACACAC[A/C]CCACACACATCTACA | 10043 |
rs199776679 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343544 | CACACACATCTACAC[A/C]CACCACACACACCTA | 10043 |
rs199813007 | snp | A/G/T | 0.000494911 | 0.0157229 | missense, intron-variant, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323515 | GGGCTGACGCGTTCC[A/G/T]CAGCTCGCCCGATCT | 10043 |
rs199899281 | snp | A/G | 9.89903e-05 | 0.00703458 | intron-variant | TOM1 | GRCh38.p7 | 22:35345823 | CCACACAGCAGGAGG[A/G]CCCGTTGTTCTCACC | 10043 |
rs199955093 | snp | C/G | 0.00208719 | 0.0322372 | missense, nc-transcript-variant, upstream-variant-2KB | TOM1, MIR6069 | GRCh38.p7 | 22:35338743 | CCCCCAAGCAACAGA[C/G]GGCCTGGCTGGAGCC | 10043 |
rs199968893 | in-del | -/CT | 0.337614 | 0.234145 | intron-variant | TOM1 | GRCh38.p7 | 22:35342979 | CACCACACCTACACA[-/CT]CATACACCTACACAC | 10043 |
rs199988305 | snp | C/T | 0.000307222 | 0.0123902 | intron-variant | TOM1 | GRCh38.p7 | 22:35323920 | CCCGGAACAGGTAAA[C/T]GAGCCTGGGGTCAGA | 10043 |
rs200020548 | in-del | -/ACA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35342874 | GCACCTACACACACC[-/ACA]CCTACACACACCACA | 10043 |
rs200049879 | snp | C/G | 0.00049478 | 0.0157209 | intron-variant | TOM1 | GRCh38.p7 | 22:35323670 | CCAAGGGAAGGGAGG[C/G]AGGACTCATCCCCAG | 10043 |
rs200072521 | snp | A/G | 0.00199792 | 0.0315431 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35327300 | CAGTGAGCTGGAGAT[A/G]GTGAGTGGGAACGTG | 10043 |
rs200104550 | in-del | -/T | | | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297473 | TTTCTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 10043 |
rs200125917 | in-del | -/CAC | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343344 | CCCCCACACACACAC[-/CAC]ACACATCTACACCCA | 10043 |
rs200204436 | in-del | -/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35329730 | CCTTTGCAGACTCAG[-/T]TTTTTTTTTGACTAA | 10043 |
rs200205732 | snp | A/G | 0.000349653 | 0.0132176 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347090 | GAACGGGCCAAAGCC[A/G]CGGACCGATTGCCCA | 10043 |
rs200235107 | in-del | -/ACAT | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301282 | TATATAAAAATATAC[-/ACAT]ACAAACATACATATA | 10043 |
rs200266300 | snp | C/G/T | 3.29773e-05 | 0.00406051 | intron-variant | TOM1 | GRCh38.p7 | 22:35317973 | AAGGGTAAGGGCCCC[C/G/T]CAAGGAGAGGTTGGG | 10043 |
rs200273234 | in-del | -/CACCCACCA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343729 | CCACACACACATCTA[-/CACCCACCA]CACCTACACACACAC | 10043 |
rs200310247 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343909 | CTGCACACACACCCC[-/A]TACACACACCACACA | 10043 |
rs200318198 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343343 | ACCCCCACACACACA[A/C]CACACACATCTACAC | 10043 |
rs200327192 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35342980 | ACCACACCTACACAC[A/T]CATACACCTACACAC | 10043 |
rs200380444 | snp | C/T | 0.00150371 | 0.0273787 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35299912 | TCCCGGGGTTGGTGG[C/T]AGCGGCGGTAGCAGC | 10043 |
rs200390952 | in-del | -/AG | | | intron-variant | TOM1 | GRCh38.p7 | 22:35311559 | GCACCTAGGCAGTGC[-/AG]AGAGCCTCAGTCGGT | 10043 |
rs200549769 | snp | A/G | 0.000249549 | 0.0111675 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347158 | CCCATCTGGCCCAGC[A/G]CCCCGGAAGAAGACC | 10043 |
rs200595303 | snp | A/G/T | 6.62892e-05 | 0.00575681 | missense, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323070 | GGGCACCGCTTCCAC[A/G/T]TGCTGGTGGCCAGCC | 10043 |
rs200639269 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35339366 | GGAGACCAGTGGCCC[A/G]GGCTTCACATTCCAG | 10043 |
rs200670439 | snp | A/G | 4.98832e-05 | 0.00499391 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35327361 | GTGCCCACCCAGGCC[A/G]AGCCCGCAGACCTGG | 10043 |
rs200699168 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343733 | ACACACATCTACACC[A/C]ACCACACCTACACAC | 10043 |
rs200711597 | snp | C/T | 0.000115799 | 0.0076083 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334496 | AGTTCGGGTGGCTCT[C/T]GGGGTTCTGGAACCC | 10043 |
rs200738877 | snp | C/T | 0.000421361 | 0.0145087 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323839 | CCAGCAAGAGGACTC[C/T]GGCCAGCATGCTGCC | 10043 |
rs200751924 | snp | A/G | 0.0121296 | 0.0769264 | intron-variant, utr-variant-5-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35299901 | TGTCAGCTGATTCCC[A/G]GGGTTGGTGGCAGCG | 10043 |
rs200766552 | snp | G/T | 0.130008 | 0.219321 | upstream-variant-2KB | TOM1 | GRCh38.p7 | 22:35297848 | TTTTGTTTTTTTTTT[G/T]TTTTTTTTTTACCAT | 10043 |
rs200895178 | snp | A/G | 0.000231187 | 0.010749 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35345782 | TGGCTGTCCACTGAC[A/G]TGGTATGTTGGGGCC | 10043 |
rs201019697 | in-del | -/CT | 0.448452 | 0.152042 | intron-variant | TOM1 | GRCh38.p7 | 22:35343369 | ACACCCACCACACAC[-/CT]CTCCACACACACCTC | 10043 |
rs201055799 | in-del | -/CA | 0.0310518 | 0.120672 | intron-variant | TOM1 | GRCh38.p7 | 22:35343106 | TACACACCCATACAC[-/CA]CACACACCCACACAC | 10043 |
rs201071632 | snp | A/G | 0.00199803 | 0.031544 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347094 | GGGCCAAAGCCGCGG[A/G]CCGATTGCCCAACCT | 10043 |
rs201085718 | snp | C/T | 0.000264227 | 0.011491 | synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35345781 | GTGGCTGTCCACTGA[C/T]GTGGTATGTTGGGGC | 10043 |
rs201184187 | in-del | -/AC/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35300905 | CCATATAAAAAAAAA[-/AC/C]CAGTTGTAATATTTA | 10043 |
rs201187142 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35312260 | AAAAAAAAAAAAAAA[C/T]ACAAGGGGAGTTCAG | 10043 |
rs201233479 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347210 | CTGTTTGCCTTATGA[C/G]TGTGGGGTCTGGCAC | 10043 |
rs201268770 | snp | C/G | 8.24097e-05 | 0.00641857 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35345740 | ATCCCAGTCACCCAG[C/G]CCTGCCTCATGGAGG | 10043 |
rs201282767 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TOM1 | GRCh38.p7 | 22:35313117 | TTTGGGAGGCCAAGG[C/T]GGGTGGATCACTTGA | 10043 |
rs201293385 | snp | C/T | 0.105214 | 0.203807 | intron-variant | TOM1 | GRCh38.p7 | 22:35343518 | ACACACTCATACACC[C/T]ACACACACCACACAC | 10043 |
rs201378027 | snp | C/G | 1.77303e-05 | 0.00297739 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323897 | GGTGACACGCCCATA[C/G]CACCAACCCCGGAAC | 10043 |
rs201378550 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35328732 | GGGGGCAGGGGACAG[C/T]GTCCACATGACAGCC | 10043 |
rs201384522 | snp | C/T | 0.00199795 | 0.0315433 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35323871 | CTCTGCCCGCCCCGC[C/T]CATACTCTCCGGTGA | 10043 |
rs201413795 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35325037 | CTGCTGAGTGACTTC[C/T]ACAGCCATGACCAGC | 10043 |
rs201416291 | snp | A/G | 0.000115398 | 0.00759512 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334410 | GTTTGACATGTTTGC[A/G]CTGACACGGGGCAGC | 10043 |
rs201431035 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35323428 | TGTCTGTTCTCTGTC[C/T]GAGTGCCAGGTGGGC | 10043 |
rs201441903 | snp | A/G | 0.000133659 | 0.00817383 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35327367 | ACCCAGGCCGAGCCC[A/G]CAGACCTGGAGCTGC | 10043 |
rs201483194 | snp | A/C | 5.30894e-05 | 0.00515188 | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347240 | CCCTGCAGCCCAGGT[A/C]CCCACTGCTCTCACA | 10043 |
rs201505071 | snp | A/G | 4.94181e-05 | 0.00497057 | intron-variant | TOM1 | GRCh38.p7 | 22:35332961 | CTGTCTCCATAACTC[A/G]TGTCTTTTCTGTCTT | 10043 |
rs201511159 | snp | C/T | 1.65455e-05 | 0.00287619 | intron-variant | TOM1 | GRCh38.p7 | 22:35322061 | CCCATCTGTCTGTCC[C/T]GTGGCAGGACTACGG | 10043 |
rs201539247 | snp | C/T | 0.000197742 | 0.00994143 | missense, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35317952 | ACATCATCAACGAGA[C/T]GGAGGAAGGGTAAGG | 10043 |
rs201573713 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301812 | ACCCCTGCCCTCCCC[A/C]GACACACACCCACCC | 10043 |
rs201590650 | snp | C/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35308238 | TGTGTGTGTCTGTCT[C/G]TCTCTCTCTCTCTTT | 10043 |
rs201629505 | in-del | -/CAT | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343135 | CACACCACACACACA[-/CAT]CTACACCCACCACAC | 10043 |
rs201689316 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343734 | CACACATCTACACCC[A/T]CCACACCTACACACA | 10043 |
rs201707838 | in-del | -/CAC | 0.0174175 | 0.0916809 | intron-variant | TOM1 | GRCh38.p7 | 22:35343679 | ACACACCCTTACACA[-/CAC]CACACCTACACACTC | 10043 |
rs201714017 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, synonymous-codon, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35317923 | GGACTGGGCCCTCAA[C/T]ATGGAGATCTGCGAC | 10043 |
rs201832515 | in-del | -/CTTGAATGG | | | intron-variant | TOM1 | GRCh38.p7 | 22:35321002 | GAAAAAAAAAAAAAA[-/CTTGAATGG]AAGGGTAAATGGACA | 10043 |
rs201859071 | in-del | -/CA | | | intron-variant | TOM1 | GRCh38.p7 | 22:35343714 | CACCTACACACACAC[-/CA]CACACACACATCTAC | 10043 |
rs201879097 | snp | C/T | 1.66632e-05 | 0.0028864 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35330362 | GAGCTCAACCGCACG[C/T]GCCGAGCCATGCAGC | 10043 |
rs201884449 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35323358 | CAACTGCGTGCTTTG[C/T]TGTGGAGTGGGCAGG | 10043 |
rs201898333 | in-del | -/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301807 | AAGGACCCCTGCCCT[-/C]CCCCGGACACACACC | 10043 |
rs201924749 | snp | A/C | | | intron-variant | TOM1 | GRCh38.p7 | 22:35342967 | CACCCCTACACACAC[A/C]ACACCTACACACTCA | 10043 |
rs201959067 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35301811 | GACCCCTGCCCTCCC[C/T]GGACACACACCCACC | 10043 |
rs202068808 | in-del | -/CCACACACACCT | 0.00358779 | 0.0422022 | intron-variant | TOM1 | GRCh38.p7 | 22:35342781 | ACACATCTACACCCA[-/CCACACACACCT]CCACACACACCTACA | 10043 |
rs202070444 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35304136 | ATCGCTTTCCAGGGT[C/T]CCACAGCCACTCAAG | 10043 |
rs202087522 | snp | C/T | 0.000387065 | 0.0139062 | intron-variant | TOM1 | GRCh38.p7 | 22:35346893 | ACCGTACTGGGGGCC[C/T]GGCTAACCTCTGCCT | 10043 |
rs202150969 | snp | G/T | 0.000265565 | 0.0115201 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35327358 | CTGGTGCCCACCCAG[G/T]CCGAGCCCGCAGACC | 10043 |
rs202171657 | in-del | -/A | | | intron-variant | TOM1 | GRCh38.p7 | 22:35309035 | ACAAGTTTCTGGCTG[-/A]AAAAAAAAATAGCTT | 10043 |
rs202189786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35306154 | TTCAGCTTTTTTTTT[C/T]CCCAACTATTTAAAA | 10043 |
rs202210239 | snp | A/C | 4.94393e-05 | 0.00497164 | intron-variant | TOM1 | GRCh38.p7 | 22:35321914 | CTCTGGTGTTAGGTA[A/C]GGGGGCTCTATTCCT | 10043 |
rs367589168 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TOM1 | GRCh38.p7 | 22:35319278 | AACAGGCTCGGCGTC[A/G]GTCAGGTGCATTGCT | 10043 |
rs367632698 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35302324 | TTTCTTTTTCTTTTT[C/T]TTTTTCTTTTTTTTT | 10043 |
rs367646858 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TOM1 | GRCh38.p7 | 22:35331161 | AGTATAGTGGCATGA[C/T]CACAGCTCACTGCAG | 10043 |
rs367650449 | snp | A/G | | | intron-variant | TOM1 | GRCh38.p7 | 22:35310763 | CCCAGGTCCCATCTG[A/G]GGTAGACAGTTAGTC | 10043 |
rs367657197 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35301038 | GCAACATGGCGAGAC[C/T]CCGTCTCTACAAAAA | 10043 |
rs367692177 | snp | A/G | 0.00127146 | 0.0251816 | intron-variant, nc-transcript-variant | TOM1, MIR3909 | GRCh38.p7 | 22:35335721 | AACTTGTCCTCTAGG[A/G]CCTGCAGTCTCATGG | 10043 |
rs367700583 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TOM1 | GRCh38.p7 | 22:35315786 | AGAAGAGGGCCCTGT[A/C]CAGTCCCGCAGAAAC | 10043 |
rs367708085 | snp | C/G | 6.23422e-05 | 0.00558276 | intron-variant, missense, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35299949 | CTTTCTCCTGGGGAA[C/G]CCGTTCAGCTCTCCA | 10043 |
rs367779490 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | TOM1 | GRCh38.p7 | 22:35339759 | AATACAAAAAATTAG[C/T]CGGGCGTGGTGGCGG | 10043 |
rs367816016 | snp | A/G | 0.000165659 | 0.00909956 | missense, nc-transcript-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35323079 | TTCCACGTGCTGGTG[A/G]CCAGCCAGGACTTCG | 10043 |
rs367957551 | snp | C/T | 6.59261e-05 | 0.00574097 | synonymous-codon, nc-transcript-variant, intron-variant, utr-variant-5-prime | TOM1 | GRCh38.p7 | 22:35322016 | GAATAAGAACTTCCA[C/T]GAGGTGATGCTGGCT | 10043 |
rs368153015 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TOM1 | GRCh38.p7 | 22:35327017 | AGTCTTCCAGCCACA[C/T]GTGGTGGCTCATTCC | 10043 |
rs368315210 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347277 | GGCTGGGACCTCCCT[C/T]CCTCCTCTGGTGTTA | 10043 |
rs368350120 | snp | C/T | 0.00019913 | 0.00997625 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334306 | TGGATGGGTCTTTCA[C/T]GTGGCCTTTCTGTCC | 10043 |
rs368387151 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TOM1 | GRCh38.p7 | 22:35330095 | CCACCCTGGCTAATA[C/T]GGCGAAACCCCGTCT | 10043 |
rs368429099 | snp | A/G | 3.30077e-05 | 0.00406236 | intron-variant, upstream-variant-2KB | TOM1, MIR3909 | GRCh38.p7 | 22:35334451 | ACCAACGGAAAGAGT[A/G]AGTGGCCTGGCCCTG | 10043 |
rs368473819 | snp | C/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35306609 | GTTCTTCAATGTCCT[C/T]GTCTGTACAATGAGG | 10043 |
rs368486186 | snp | C/T | 1.66338e-05 | 0.00288386 | missense, nc-transcript-variant | TOM1 | GRCh38.p7 | 22:35347157 | CCCCATCTGGCCCAG[C/T]GCCCCGGAAGAAGAC | 10043 |
rs368590463 | snp | C/T | 1.68454e-05 | 0.00290214 | intron-variant | TOM1 | GRCh38.p7 | 22:35346882 | GCCCCAGGCTGACCG[C/T]ACTGGGGGCCCGGCT | 10043 |
rs368635378 | snp | A/T | | | intron-variant | TOM1 | GRCh38.p7 | 22:35330942 | TCAGAATCCAGAGAA[A/T]AGTGAAACTGATGTC | 10043 |
rs368762469 | snp | C/G/T | 3.29453e-05 | 0.00405854 | intron-variant | TOM1 | GRCh38.p7 | 22:35332976 | GTGTCTTTTCTGTCT[C/G/T]GTAGGTTTGAACGGT | 10043 |