SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1745 | snp | A/G | 0.423881 | 0.179625 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021306 | TTCACTGGGGGTCTT[A/G]GAACGTATGTCCCAT | 7110 |
rs15780 | snp | A/C | 0.449091 | 0.151204 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021248 | TATATGTATAGGAAA[A/C]AACAGTGTATAGAGG | 7110 |
rs937858 | snp | A/C | 0.40108 | 0.199185 | intron-variant | TMF1 | GRCh38.p7 | 3:69033722 | CATTGGTAATGACTT[A/C]AGAATTTCATGATTC | 7110 |
rs937859 | snp | A/G | 0.454295 | 0.144096 | intron-variant | TMF1 | GRCh38.p7 | 3:69033506 | TGCAGAAGCTCTTCC[A/G]TCTTGTTTATAGAAT | 7110 |
rs1044302 | snp | A/T | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020190 | ATGTTCAGGAAATTT[A/T]TTTTCTCCATCTCTT | 7110 |
rs1053555 | snp | G/T | 0.480931 | 0.0957637 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021412 | GTCAGCTTGATTTTT[G/T]TGTGTGTGTAATATT | 7110 |
rs1246013 | snp | A/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69042047 | ttattttatttattt[A/T]tttttttgatacaaa | 7110 |
rs1344931 | snp | A/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69033286 | ATTCAGTTCTTTTTT[A/T]TTTTTTTTTTTGATA | 7110 |
rs1463957 | snp | A/G | 0.470618 | 0.117591 | intron-variant | TMF1 | GRCh38.p7 | 3:69044846 | TAGATCCCCAACTAG[A/G]TATTGCCTAATTGTT | 7110 |
rs1532918 | snp | C/G | 0.190055 | 0.242717 | missense | TMF1 | GRCh38.p7 | 3:69033557 | GAGAAGAATCTTTCT[C/G]ATAGGCTTGGTAACT | 7110 |
rs2055685 | snp | C/G | 0.45479 | 0.161862 | intron-variant | TMF1 | GRCh38.p7 | 3:69034911 | ATTCAGCAAATGCTA[C/G]GTGTGACAGTAATCC | 7110 |
rs2271118 | snp | A/G | 0.305759 | 0.243703 | intron-variant | TMF1 | GRCh38.p7 | 3:69044447 | ACACATTTTCTGGAA[A/G]CCTGTATACTTTGTA | 7110 |
rs2271119 | snp | C/T | 0.44546 | 0.155869 | intron-variant | TMF1 | GRCh38.p7 | 3:69044240 | TTTTAGTATTAGAGA[C/T]TTAAAACGTATTTGA | 7110 |
rs2271120 | snp | A/G | 0.378045 | 0.214719 | intron-variant | TMF1 | GRCh38.p7 | 3:69042565 | CCCTGTAAAATAGAC[A/G]GAAATTTGTGCTGCC | 7110 |
rs2271121 | snp | A/C | 0.41979 | 0.183497 | intron-variant | TMF1 | GRCh38.p7 | 3:69035010 | TTTGTGTTTTGGAAA[A/C]CTGTGACAGTACCTG | 7110 |
rs2271122 | snp | C/T | 0.385359 | 0.210185 | intron-variant | TMF1 | GRCh38.p7 | 3:69035283 | TTCATCAAGCAATTC[C/T]AAAACTGTATGTATA | 7110 |
rs2279936 | snp | A/G | 0.29432 | 0.24604 | intron-variant | TMF1 | GRCh38.p7 | 3:69025779 | TCCATTACCAGGTTC[A/G]AACAAAAATGGTTCT | 7110 |
rs2292199 | snp | C/T | 0.32291 | 0.239132 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69047463 | TATCTTGGTTTCTTC[C/T]ACACCAATAAATGAA | 7110 |
rs2314230 | snp | C/T | 0.45946 | 0.136478 | intron-variant | TMF1 | GRCh38.p7 | 3:69045743 | CAGGGCAAGACTCCG[C/T]CTCAAAAAATAAATA | 7110 |
rs2314231 | snp | A/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69046520 | AATCTGGCACTTTTT[A/T]AAAAAATTAAGTAAT | 7110 |
rs3732628 | snp | A/G | 0.459914 | 0.13578 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049284 | GAGGCTGAGGTGGGA[A/G]GATCATCTGAGCCCA | 7110 |
rs3736422 | snp | C/T | 9.93772e-05 | 0.00704831 | missense | TMF1 | GRCh38.p7 | 3:69038670 | CTCAGAGCAGCTTCC[C/T]GTGCCTCACTATCCT | 7110 |
rs3772976 | snp | A/G | 0.395453 | 0.203331 | intron-variant | TMF1 | GRCh38.p7 | 3:69024259 | ATAAAAATATTTAAT[A/G]TGTGTGTGGTTTTTT | 7110 |
rs3772977 | snp | C/T | 0.178144 | 0.239451 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050785 | CTGACTTTTCAATGA[C/T]GTAAAATTAAGAACA | 7110 |
rs3817105 | snp | A/G | 0.448452 | 0.152042 | intron-variant | TMF1 | GRCh38.p7 | 3:69044226 | ATTTAAAACGTATTT[A/G]AAGAAAACTGTGTTA | 7110 |
rs3836333 | in-del | -/ATTT | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024421 | GAGATAAATCCAATT[-/ATTT]GTTTGAAAACATTCA | 7110 |
rs4855351 | snp | A/G | 0.467337 | 0.123551 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69054106 | GAACAGAAAACTGCC[A/G]TATCTAAGTCAAAAA | 7110 |
rs4855352 | snp | A/G | 0.467744 | 0.122832 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69054142 | AATGAGAACACATAC[A/G]TGTTCTCATATTAAA | 7110 |
rs6549177 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | TMF1 | GRCh38.p7 | 3:69037322 | ACACGCTGAAACCCC[A/G]TGTCTACTAAAAATA | 7110 |
rs6549178 | snp | G/T | 0.47614 | 0.106587 | intron-variant | TMF1 | GRCh38.p7 | 3:69042057 | TATTTATTTTTTTGA[G/T]ACAAAGTCTCACTCT | 7110 |
rs6765571 | snp | A/G | 0.45645 | 0.140991 | intron-variant | TMF1 | GRCh38.p7 | 3:69031571 | tattaggcaatgtgt[A/G]caaaggacctttcta | 7110 |
rs6767963 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TMF1 | GRCh38.p7 | 3:69031333 | aaaaagaaaaaaagc[C/T]aacaggaaggactca | 7110 |
rs6801855 | snp | C/T | 0.0607341 | 0.163335 | intron-variant | TMF1 | GRCh38.p7 | 3:69031628 | tctacattatatcaa[C/T]aaaaattttcaattg | 7110 |
rs7375020 | snp | A/G | 0.487432 | 0.0782705 | intron-variant | TMF1 | GRCh38.p7 | 3:69024766 | AAAAGAGGTATCCTG[A/G]TTCAAAATGCTTGAG | 7110 |
rs7426611 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049570 | TTCTCAAATTCTAAA[C/T]TATGTCAGAAATTAC | 7110 |
rs7429868 | snp | C/T | 0.0577344 | 0.159793 | intron-variant | TMF1 | GRCh38.p7 | 3:69030784 | aaaacagggacgaca[C/T]aaaatgttggcaagg | 7110 |
rs7612705 | snp | C/T | 0.0748431 | 0.178382 | intron-variant | TMF1 | GRCh38.p7 | 3:69025212 | CTTCCCTTTATTCTG[C/T]TGGGAAAGAGCTGCT | 7110 |
rs8179890 | snp | A/G | 0.0228355 | 0.104385 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022510 | GGATAGGTACCAAAA[A/G]GTACCACATTTTATA | 7110 |
rs9809889 | snp | G/T | 0.488786 | 0.0740357 | intron-variant | TMF1 | GRCh38.p7 | 3:69038261 | CAGGAGTTAAATGGA[G/T]TCTCTCAAAATTATA | 7110 |
rs9811018 | snp | C/T | 0.00380945 | 0.0434766 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038905 | AAGTTCATCCATGTC[C/T]ACCTGAAGACGGCCA | 7110 |
rs9813514 | snp | A/G | 0.397271 | 0.202018 | intron-variant | TMF1 | GRCh38.p7 | 3:69031030 | aatggttaaatatac[A/G]tggtacatactatgg | 7110 |
rs9813815 | snp | A/G | 0.021333 | 0.101051 | intron-variant | TMF1 | GRCh38.p7 | 3:69031231 | ttagtgattgccaga[A/G]atttgggacaaggga | 7110 |
rs9826616 | snp | A/C | 0.405255 | 0.195948 | intron-variant | TMF1 | GRCh38.p7 | 3:69026621 | GTAAAACTCAGTCTC[A/C]AAAACAAACAAACAA | 7110 |
rs9855731 | snp | A/G | 0.254664 | 0.249956 | intron-variant | TMF1 | GRCh38.p7 | 3:69028046 | GTAATTCATGCCATG[A/G]TAAGTCAATCTCAAA | 7110 |
rs9862298 | snp | C/T | 0.487432 | 0.0782705 | intron-variant | TMF1 | GRCh38.p7 | 3:69023610 | TAAGCACACTTGATA[C/T]AAAATTTAGTCTCTT | 7110 |
rs9985501 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | TMF1 | GRCh38.p7 | 3:69042489 | TAAATCCCAGAGTTA[C/T]ACACTTTGAATGTCT | 7110 |
rs10681795 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024823 | TTTTTTTTTTTTTTT[-/T]CAGATTATGGAATAA | 7110 |
rs10707788 | in-del | -/G | 0.468249 | 0.121932 | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054291 | GGGGGGCGGGGGGGG[-/G]TGGATCACCTGAGGT | 7110 |
rs10865643 | snp | A/G | 0.415235 | 0.18761 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050595 | CAAATATCCTTATAT[A/G]TAAAACCTATATTCT | 7110 |
rs11128108 | snp | C/T | 0.443598 | 0.158176 | intron-variant | TMF1 | GRCh38.p7 | 3:69036694 | TGTAAATGTTTTACA[C/T]ATACAAAACTTAAAA | 7110 |
rs11128109 | snp | C/T | 0.44768 | 0.153045 | intron-variant | TMF1 | GRCh38.p7 | 3:69037312 | ATCCTGGCTAACACG[C/T]TGAAACCCCATGTCT | 7110 |
rs11128110 | snp | A/G | 0.448963 | 0.151372 | intron-variant | TMF1 | GRCh38.p7 | 3:69044164 | TCTGAATCTTCTTGT[A/G]TCACATTTTCCCAAT | 7110 |
rs11318005 | in-del | -/A | 0.488606 | 0.0746142 | intron-variant | TMF1 | GRCh38.p7 | 3:69027680 | AATAGCTGATGAACT[-/A]AAAAAAAAAAAAAAA | 7110 |
rs11338290 | in-del | -/T | 0.390277 | 0.206936 | intron-variant | TMF1 | GRCh38.p7 | 3:69028724 | AGGAAGAACAGAGGG[-/T]TAAAAAATACTAACC | 7110 |
rs11447014 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032613 | TTTTTTTTTTTTTTT[-/T]GAGATGCAGTCTCGC | 7110 |
rs11557640 | snp | A/G | | | missense | TMF1 | GRCh38.p7 | 3:69027959 | TTAGAAATTTAAAGA[A/G]TGAAAGTTGAACAAG | 7110 |
rs12054469 | snp | C/G | 0.428182 | 0.17536 | intron-variant | TMF1 | GRCh38.p7 | 3:69042086 | CTGTCGCCCAGGCTG[C/G]AGTACAGTGGCGTGA | 7110 |
rs12489922 | snp | C/T | 0.462034 | 0.132445 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053849 | ACCATCTAAAACTAT[C/T]TATTCAGCTCTCAGA | 7110 |
rs12636843 | snp | C/T | 0.0372196 | 0.131242 | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054241 | AAAAACATggtcagg[C/T]atggtggctcatgcc | 7110 |
rs13063094 | snp | A/T | 0.409891 | 0.192184 | intron-variant | TMF1 | GRCh38.p7 | 3:69027000 | TTTATTTATTTATTT[A/T]TTTTTATTTTTTTGA | 7110 |
rs13068103 | snp | A/G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69040751 | ACATGGTGAAACCCC[A/G/T]TCTCTACTAAAAATA | 7110 |
rs13071583 | snp | A/T | 0.445592 | 0.155704 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050957 | AGATCCCTGAAAGAT[A/T]AAGCTCAATGAAACT | 7110 |
rs13073272 | snp | A/G | 0.487177 | 0.0790385 | intron-variant | TMF1 | GRCh38.p7 | 3:69034024 | TTCATCATGTTGCTC[A/G]GGCTGGCCTCGAACT | 7110 |
rs13073502 | snp | A/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034166 | GTTAGATTGTGTAAT[A/C]CAGTATCTAAATAAG | 7110 |
rs13079161 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69041982 | TTCAGTATCCATTTG[G/T]AATGATTTATTTCAT | 7110 |
rs13084180 | snp | A/T | 0.117188 | 0.211804 | intron-variant | TMF1 | GRCh38.p7 | 3:69045961 | ctagagcggattagg[A/T]gggaggactgcttga | 7110 |
rs13094896 | snp | C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034445 | gccactgcactcctg[C/G]ctgggcaacagagca | 7110 |
rs13095343 | snp | C/G | 0 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69041932 | CACGTTTTCCAAAGG[C/G]TCCTCTCTCCCAGGA | 7110 |
rs13099820 | snp | A/G | 0.400325 | 0.199756 | intron-variant | TMF1 | GRCh38.p7 | 3:69035522 | GCCTTTTTGGAAAAC[A/G]TTATAATATGTTTAA | 7110 |
rs13319158 | snp | G/T | 0.067446 | 0.170804 | intron-variant | TMF1 | GRCh38.p7 | 3:69051044 | GTCACACATTTTCCG[G/T]CTAATACCTCCGGCA | 7110 |
rs17005231 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | TMF1 | GRCh38.p7 | 3:69030105 | TAATGATGCAAGTAG[C/T]CACACTTAAAACTGA | 7110 |
rs17005239 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | TMF1 | GRCh38.p7 | 3:69031898 | GTACCAGTTTCTAGC[A/G]TTCATTTATTGCTAA | 7110 |
rs17005254 | snp | A/C | 0.480223 | 0.0974544 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049788 | ATAATCAGGATCTTA[A/C]AAATGGTATATTCGT | 7110 |
rs17048274 | snp | A/G | 0.0431256 | 0.140367 | intron-variant | TMF1 | GRCh38.p7 | 3:69023330 | CAAATCCTGAAAAAT[A/G]TATTTGTTTACAATT | 7110 |
rs28372813 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB, utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052378 | CTCCCGGATGTGACG[C/T]CAACGTTCTTCTGTT | 7110 |
rs28480268 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69028471 | TCTGAGTTTCACTCA[G/T]AAACCAAACCAAAAG | 7110 |
rs34091520 | in-del | -/AC | 0.344147 | 0.231595 | intron-variant | TMF1 | GRCh38.p7 | 3:69031417 | TGTTTAGAACTTAAT[-/AC]ACACACACACACACA | 7110 |
rs34175383 | snp | A/G | 0.442791 | 0.15916 | intron-variant | TMF1 | GRCh38.p7 | 3:69051739 | ACCAAAGAAAGACAA[A/G]GGGGAACCTGGATCT | 7110 |
rs34206158 | snp | C/G/T | 0.00113433 | 0.0237884 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69047880 | TGTAGTCTCTTGTCT[C/G/T]GAGCTCGCTGAGCTC | 7110 |
rs34224196 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69044469 | AAATGTGTAACATTA[-/T]TTCACATTTGCAGAA | 7110 |
rs34283375 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69039713 | GATGGTAAAGAAGTA[-/T]TAAACTCAAATGATA | 7110 |
rs34428015 | snp | C/T | 0.0101778 | 0.0706068 | missense | TMF1 | GRCh38.p7 | 3:69047362 | ACTAGAGTTACCTTG[C/T]AAACATCTTCCTTCT | 7110 |
rs34504690 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69046901 | AATAATTAAAATCTT[-/A]AATTATCATTTAATA | 7110 |
rs34547039 | in-del | -/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69028193 | ATTCTCTAATGTATG[-/C]CCTAAGAGCTGAGTG | 7110 |
rs34778745 | in-del | -/A | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69033292 | GTGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA | 7110 |
rs34917634 | snp | A/G | 0.00870681 | 0.0654033 | missense | TMF1 | GRCh38.p7 | 3:69038653 | TAGCTTTCATTTCAC[A/G]GCTCAGAGCAGCTTC | 7110 |
rs34956334 | in-del | -/AA | 0.379354 | 0.213933 | intron-variant | TMF1 | GRCh38.p7 | 3:69046303 | TGGACTCAAAAAAAT[-/AA]AGTCTTACCTGAGTT | 7110 |
rs35069139 | in-del | -/G | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021973 | CAGGCATGAGCCACA[-/G]GCACCTGGCCGTAAA | 7110 |
rs35347565 | in-del | -/T | 0.15698 | 0.23205 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021685 | TTAAATAAGAGTTTG[-/T]TTTTTTTTTTTTTGA | 7110 |
rs35447207 | snp | C/G | 0.000832237 | 0.020382 | missense | TMF1 | GRCh38.p7 | 3:69047417 | CAGCAGGTTCACACT[C/G]CTCAGCCACCTTGTC | 7110 |
rs35708142 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69040432 | GGGAGATGTAGACTG[-/A]AAGAATTTAGGAGCA | 7110 |
rs35783734 | snp | A/G | 0.00884184 | 0.0658995 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69023240 | ATTTTTTACATCTTC[A/G]AGATCTAATCGAAGT | 7110 |
rs35856064 | snp | A/G | 0.000873377 | 0.0208788 | missense | TMF1 | GRCh38.p7 | 3:69028261 | CAAGTGTTCTTACAT[A/G]TTCATCTTTTAGGTT | 7110 |
rs35933614 | in-del | -/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69027606 | TCCAATCTTTTGGTT[-/C]CCCTGGGCCTCATTT | 7110 |
rs35970969 | snp | A/G | 0.0256215 | 0.110247 | intron-variant | TMF1 | GRCh38.p7 | 3:69029540 | ACTTCCGCCTCCCGG[A/G]TGTAAGCGATTCTCA | 7110 |
rs36000302 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69027756 | TGTTGGGCTTCATTC[-/A]AAAATCATCCTGGGC | 7110 |
rs41291189 | snp | A/G | 0.101282 | 0.200955 | intron-variant | TMF1 | GRCh38.p7 | 3:69025727 | CCTATGTTAATTAAG[A/G]AAGTTCACACAGTTA | 7110 |
rs41291191 | snp | A/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029518 | GGTGGGATCTTGGCT[A/C]ACTGCAACTTCCGCC | 7110 |
rs41291193 | snp | C/T | 1.6563e-05 | 0.00287771 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69035032 | CAGTACCTGCTGAAG[C/T]TCACCGATCTCATGG | 7110 |
rs41291195 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | TMF1 | GRCh38.p7 | 3:69039115 | AATATATATTTTTTT[G/T]AGACAAAGTCTCGCT | 7110 |
rs41291197 | snp | C/T | 0.0850919 | 0.187897 | utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052218 | GTGTGGCCATTACCC[C/T]GACAGCCTCCCGCGA | 7110 |
rs56002120 | snp | A/G | 0.0314385 | 0.121371 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020823 | AGAAATTGTTAATAC[A/G]GATAAAAAAAGAATG | 7110 |
rs57258153 | in-del | -/A | | | frameshift-variant | TMF1 | GRCh38.p7 | 3:69038963 | GAATTTAGTTTTTTA[-/A]TATTTTCTCTATGTT | 7110 |
rs57404870 | in-del | -/TAA/TAATAGAGTAG | | | intron-variant | TMF1 | GRCh38.p7 | 3:69036014 | TTTTATCTATCCCAG[-/TAA/TAATAGAGTAG]CAGAAACACAAAGGA | 7110 |
rs57789461 | snp | C/T | 0.420096 | 0.183214 | intron-variant | TMF1 | GRCh38.p7 | 3:69040696 | CTTTTGGGAAGCAGG[C/T]GGATCACCAGAGGTC | 7110 |
rs59034553 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054290 | GGAAGCCGAGGGGGG[C/T]GGGGGGGGGTGGATC | 7110 |
rs59157330 | snp | A/T | 0.42263 | 0.180829 | intron-variant | TMF1 | GRCh38.p7 | 3:69041413 | TAAATATTAGTTGAA[A/T]AAATGAAAAAGTTGG | 7110 |
rs59516442 | in-del | -/AC/CA | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031418 | ACACACACACACACA[-/AC/CA]TACACAAATGAGTAC | 7110 |
rs61737463 | snp | C/G | 0.000198913 | 0.00997079 | missense | TMF1 | GRCh38.p7 | 3:69029928 | CTCCATGGAAGACAT[C/G]TGAATTTTGTTAGCA | 7110 |
rs61737464 | snp | C/T | 0.0065301 | 0.0567662 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69029886 | TTGAAATCTACTGTT[C/T]TCCTGTCTTAAAAGA | 7110 |
rs62254199 | snp | G/T | 0.455263 | 0.142713 | intron-variant | TMF1 | GRCh38.p7 | 3:69026721 | TTACAACAATGTAAT[G/T]TGTTGGGTTTTTATA | 7110 |
rs62254200 | snp | A/C | 0.470521 | 0.117772 | intron-variant | TMF1 | GRCh38.p7 | 3:69029519 | GTGGGATCTTGGCTC[A/C]CTGCAACTTCCGCCT | 7110 |
rs62254236 | snp | C/G | 0.447938 | 0.152711 | intron-variant | TMF1 | GRCh38.p7 | 3:69037926 | CTTGGCAAGGATGTG[C/G]AGAAACTGAAACCCT | 7110 |
rs62254240 | snp | G/T | 0.0685596 | 0.171987 | intron-variant | TMF1 | GRCh38.p7 | 3:69051249 | TAGGAGGCCGAGGTG[G/T]GTGGATCGCCTTAAG | 7110 |
rs67036817 | snp | C/T | 0.459118 | 0.137002 | intron-variant | TMF1 | GRCh38.p7 | 3:69039793 | AAGAACAGAATTTTT[C/T]TAAATTACAATTTTG | 7110 |
rs67138835 | snp | A/T | 0.455858 | 0.141853 | intron-variant | TMF1 | GRCh38.p7 | 3:69026640 | ACAAACAAACAAAAA[A/T]AAAGTACAATATTTA | 7110 |
rs67270234 | in-del | -/T | 0.391397 | 0.206172 | intron-variant | TMF1 | GRCh38.p7 | 3:69029450 | TACTTATTTAATTTA[-/T]TTTTTTTTTTTTGAG | 7110 |
rs71112685 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024823 | AATGTTTCAAATTTC[-/T]TTTTTTTTTTTTTTT | 7110 |
rs71302164 | snp | C/T | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69035842 | ATTATGAAAAACACA[C/T]ATATGGGAATAGAAT | 7110 |
rs72184346 | in-del | -/CA | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031427 | TTAATACACACACAC[-/CA]ACACACACATACACA | 7110 |
rs72922993 | snp | A/C | 0.0221141 | 0.102801 | intron-variant | TMF1 | GRCh38.p7 | 3:69029354 | TCCTATTACTAATAA[A/C]CCTAACTTTAAATGC | 7110 |
rs72923000 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69041325 | TTCCCTCTCACTGAA[C/G]TAAGCCCCTAAAGGA | 7110 |
rs73110228 | snp | C/T | 0.00810874 | 0.0631555 | missense | TMF1 | GRCh38.p7 | 3:69047989 | GGAGAAGGTGTATTG[C/T]TCTGCCTGTCTTCAT | 7110 |
rs74803787 | snp | A/G | 0.0524604 | 0.153226 | intron-variant | TMF1 | GRCh38.p7 | 3:69044671 | TGCAGGTGTATCACT[A/G]TAACAAAGAAAACAG | 7110 |
rs75062243 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | TMF1 | GRCh38.p7 | 3:69051820 | ATTAGGGAACGGGCC[A/G]GGGAGAAATTACTTC | 7110 |
rs75120589 | snp | A/C | 0 | 0 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019651 | AGTGAGACTCTGTCA[A/C]AAAAAAAAAAAAAAA | 7110 |
rs75189109 | snp | A/T | 0 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69027694 | TAAAAAAAAAAAAAA[A/T]AATCATGAAAAAAAT | 7110 |
rs75784205 | snp | A/T | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69027563 | TTGATTTTAGACATT[A/T]AAAAAATGATACTTA | 7110 |
rs75844324 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | TMF1 | GRCh38.p7 | 3:69039791 | AAAAGAACAGAATTT[C/T]TTTAAATTACAATTT | 7110 |
rs76143707 | snp | G/T | 0.0170251 | 0.090679 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052551 | GTGTGTGCTTTCCAG[G/T]AAAATAGTTCACGTG | 7110 |
rs76352061 | snp | A/C | 0.0107246 | 0.0724382 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020446 | TAAATGACCAAACAA[A/C]CTTCCCTTTGTTTAC | 7110 |
rs76673769 | snp | G/T | 0 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69029461 | TTTATTTTTTTTTTT[G/T]TGAGACCGAGTCTCA | 7110 |
rs76863529 | snp | C/T | 0.000580128 | 0.0170214 | missense | TMF1 | GRCh38.p7 | 3:69048146 | CAGTTGGCACCTTCA[C/T]ATCCGATTCTTTATT | 7110 |
rs76969854 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TMF1 | GRCh38.p7 | 3:69038127 | ATTGATAATAACCAC[A/G]AAGTATAAATAACCC | 7110 |
rs77200446 | snp | A/G | 0.0368353 | 0.130617 | intron-variant | TMF1 | GRCh38.p7 | 3:69035342 | TTAAGGCAAAGAAAC[A/G]CAAACAAATATGTAT | 7110 |
rs77651017 | snp | A/C | 0.5 | 0 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019649 | AGAGTGAGACTCTGT[A/C]AAAAAAAAAAAAAAA | 7110 |
rs77811522 | snp | A/G | 0.0372196 | 0.131242 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050400 | CACAATATCCAAACC[A/G]GAGAAAATCAAAATT | 7110 |
rs77956399 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021110 | AAGATATTTTGAGAG[A/G]AAGAGACAGACATAT | 7110 |
rs78048968 | snp | C/G | | | missense | TMF1 | GRCh38.p7 | 3:69033646 | CGAAGCAATGGTCTT[C/G]TTGTTGATGAAACAC | 7110 |
rs78062898 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | TMF1 | GRCh38.p7 | 3:69041392 | TCTGACATACTAACC[A/G]TTCAATAAATATTAG | 7110 |
rs78189636 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69036557 | TGCATTTTGCCAATA[A/G]AAACACTGAAAAGAT | 7110 |
rs78265570 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69040426 | TGCCCTTGGGAGATG[C/T]AGACTGAAGAATTTA | 7110 |
rs78362922 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | TMF1 | GRCh38.p7 | 3:69026679 | AACTGTAGCTAGACT[C/T]GGTTAGATCATCACA | 7110 |
rs78391797 | snp | A/G | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69037316 | TGGCTAACACGCTGA[A/G]ACCCCATGTCTACTA | 7110 |
rs78417479 | snp | A/G | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69025799 | AAAATGGTTCTGTCA[A/G]TTTTTGCTTTAAATG | 7110 |
rs79092593 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050261 | TGAGACTGTGTCTCA[A/C]AAAAAAAAAAAACAA | 7110 |
rs79188160 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TMF1 | GRCh38.p7 | 3:69031256 | AAGGGAGGAAGGGTT[A/G]AGAGAGTGGTAGGTG | 7110 |
rs79837835 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | TMF1 | GRCh38.p7 | 3:69023884 | AAAATTACTTTGAAT[A/C]TGTAAAGATACAAGC | 7110 |
rs80190297 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050985 | ACTGCAAAGAGAGAC[C/T]TGGCTATTCAGAAAT | 7110 |
rs111259740 | in-del | -/A | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69037486 | TCTACTAAAAAAAAA[-/A]CAAAAATTAGCCGGG | 7110 |
rs111542457 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TMF1 | GRCh38.p7 | 3:69038497 | ATTCAAACCAGCTAA[C/T]TGTTTAATTTGTAGA | 7110 |
rs111681194 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TMF1 | GRCh38.p7 | 3:69034292 | AGCCTGGCCAACATG[A/G]TGAAACCTCATCTCT | 7110 |
rs111773236 | snp | C/T | 0 | 0 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048941 | AACACGCTTTACTTA[C/T]CAATATGAAATAAAC | 7110 |
rs112062832 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69028898 | TTTGTGGTGTTATAG[A/G]CCCCTTTAAAAAATC | 7110 |
rs112081936 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | TMF1 | GRCh38.p7 | 3:69030555 | GAGTGAGAGCAAATA[A/T]ATGCAAACCATATAT | 7110 |
rs112237586 | snp | C/T | 0.00302083 | 0.0387465 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69024055 | GTGAAGAATACTTAC[C/T]CTTAGCTGAGTTCTA | 7110 |
rs112260113 | snp | C/G | 0 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69029085 | GCTCTGCTGCCCGGG[C/G]TGGGGTGCAATGGTG | 7110 |
rs112282331 | snp | A/T | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69028725 | GGAAGAACAGAGGGT[A/T]AAAAAATACTAACCA | 7110 |
rs112349668 | snp | G/T | 0.00307324 | 0.0390791 | intron-variant | TMF1 | GRCh38.p7 | 3:69033518 | AGATGGAAGAGCTTC[G/T]GCATCGAGCATAAAA | 7110 |
rs112573478 | snp | A/G | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049232 | TTTTTTAATTAGCTG[A/G]GCCTGGTGGCCCACA | 7110 |
rs112674466 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | TMF1 | GRCh38.p7 | 3:69035597 | CTTGGGAATTCACTC[C/T]AAGAAAGCAGATACG | 7110 |
rs112888785 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69051632 | TCAGGTTCGGGAAGG[C/T]TGTGCTTGGAAGCTG | 7110 |
rs113488852 | snp | G/T | 0.5 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69030975 | GCTTTATCTGTAATA[G/T]CCAGAGCTTGGAATC | 7110 |
rs113557115 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029328 | ATGAGCCACAGCACC[C/T]GGCCATAATATCCTA | 7110 |
rs113572356 | snp | G/T | 0.0256215 | 0.110247 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021689 | AATAAGAGTTTGTTT[G/T]TTTTTTTTTGAGACG | 7110 |
rs113699639 | snp | A/G | 0.0850919 | 0.187897 | intron-variant | TMF1 | GRCh38.p7 | 3:69027059 | GGAATGCAGTGATGC[A/G]ATCTCGGCTCACTGC | 7110 |
rs113762398 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021315 | GGTCTTGGAACGTAT[C/G]TCCCATGGGTAAGAG | 7110 |
rs113762789 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053740 | GCTAAGTAGTCTGCA[A/G]AGGAGATTTGGGGCA | 7110 |
rs113852987 | snp | A/G | 0.0123036 | 0.0774623 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021614 | ACTCCAAATTCTTCA[A/G]GATGGTGTACTTGTA | 7110 |
rs113891605 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | TMF1 | GRCh38.p7 | 3:69039107 | TGGAGAAAAATATAT[A/G]TTTTTTTGAGACAAA | 7110 |
rs113928467 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant | TMF1 | GRCh38.p7 | 3:69033013 | ACCAGTGATGAGAAT[A/C]ATATATGATCTCTAC | 7110 |
rs114327621 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020149 | TTAATAAGCATTCAA[A/G]TAAAACTCTCAATAA | 7110 |
rs114391109 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69046526 | GCACTTTTTTAAAAA[A/T]TTAAGTAATTCAATA | 7110 |
rs114445898 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050177 | AGGCACGAGAATCAC[A/T]TGAGCTCAGGAGACA | 7110 |
rs114516559 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022465 | TATCCAATCACATCT[A/G]GATAACATTGAATAT | 7110 |
rs114583253 | snp | A/G | 0.030665 | 0.119967 | intron-variant | TMF1 | GRCh38.p7 | 3:69029737 | TGAGCCACGGCGCCC[A/G]GCCCAACAACATACT | 7110 |
rs114633541 | snp | A/C | 0.0524604 | 0.153226 | intron-variant | TMF1 | GRCh38.p7 | 3:69045413 | CAGTGAGCCAAGATT[A/C]TGCAATGATCTTGCA | 7110 |
rs114647798 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | TMF1 | GRCh38.p7 | 3:69023564 | ACTAAATCTACAATT[C/G]TCCCCATATATGACT | 7110 |
rs114699684 | snp | A/G/T | 0.00811315 | 0.0631732 | intron-variant | TMF1 | GRCh38.p7 | 3:69035156 | ACAAACAATGGTACA[A/G/T]TATTATCTATAACTT | 7110 |
rs114833972 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69030062 | GCCCAGAGACCAAAA[C/T]ACCAAGTCAATTCTG | 7110 |
rs114933016 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | TMF1 | GRCh38.p7 | 3:69026283 | TCTAATTTCCCCATA[A/C]AATGGCTTCTTAAGT | 7110 |
rs115066528 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | TMF1 | GRCh38.p7 | 3:69028622 | CAAAGCTTATTAGGG[A/G]GTTCTATGAAAATGT | 7110 |
rs115068738 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TMF1 | GRCh38.p7 | 3:69035500 | GCATACATTATAAAC[C/T]ACCATAGCCTTTTTG | 7110 |
rs115124158 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69041705 | ATTGGAAATTAAATA[A/T]ATGATCTTAAATATG | 7110 |
rs115175344 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | TMF1 | GRCh38.p7 | 3:69043312 | GTAGTTGGGACCACA[C/T]GCATGTACCACCATG | 7110 |
rs115301130 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022779 | GTTTCAGTATGTTAA[C/T]ATTACTCTTCAAATG | 7110 |
rs115312566 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69045019 | ACCAAAAGAAGAAGG[A/G]AGATGGATGCAATCA | 7110 |
rs115392935 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69046105 | TAGAGAGAGACCCTG[G/T]CTCATTCATACATAC | 7110 |
rs115419890 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69046269 | ACTTGAGTATAAAAG[A/G]AGTAGGAAGGGTTCC | 7110 |
rs115454012 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TMF1 | GRCh38.p7 | 3:69035383 | CATTACCATACAATA[C/T]TGGAGAAAAGACAGT | 7110 |
rs115455462 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | TMF1 | GRCh38.p7 | 3:69045741 | AACAGGGCAAGACTC[C/T]GCCTCAAAAAATAAA | 7110 |
rs115463665 | snp | C/G | 0.0275645 | 0.114116 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052445 | GGTTTCTATTGATGT[C/G]GATTTCGTGCTTACA | 7110 |
rs115508565 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | TMF1 | GRCh38.p7 | 3:69034587 | AACCTCTTAGTAGTT[A/G]CCTCCTCATCCAAAT | 7110 |
rs115537508 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021093 | GGTGAGTACAGTACA[A/G]TAAGATATTTTGAGA | 7110 |
rs115614766 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049218 | CCCTACAAAAAAATT[G/T]TTTTAATTAGCTGGG | 7110 |
rs115684987 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69031770 | CTCCACAGCATAGCT[A/G]TGGTCTTTTTAATAG | 7110 |
rs115768674 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69040049 | TGATATAGTTGTTCA[A/G]TATCACCCAGATATT | 7110 |
rs115826511 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | TMF1 | GRCh38.p7 | 3:69044035 | AGAAAAAAAAAGGAA[A/G]TTTCCCTTGTTAAAT | 7110 |
rs115971285 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69032269 | TCTAGTTCACCCCCC[C/T]GATTCACAAGGAATA | 7110 |
rs116084337 | snp | C/T | 0.001941 | 0.0310923 | intron-variant | TMF1 | GRCh38.p7 | 3:69047327 | TCTCCAAAAAGCACA[C/T]CTAAAAATCCCTTCC | 7110 |
rs116277435 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69032580 | ACAGAAGGGCAACCT[C/G]GGGCATGACTGTAAA | 7110 |
rs116364410 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69038188 | CAAAGCCTCACAAAT[C/T]TTGTTTTTCCTACTT | 7110 |
rs116383007 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049358 | CAGCCTGGGTGACAG[A/G]TCGAGAACCTGTCTC | 7110 |
rs116415392 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69031930 | TATTTATTTCAAAAG[A/C/G]TATCATTTTCAGATG | 7110 |
rs116685603 | snp | A/G | 0.0275645 | 0.114116 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052458 | GTCGATTTCGTGCTT[A/G]CAGCAGTTCTTAGCG | 7110 |
rs116829898 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | TMF1 | GRCh38.p7 | 3:69039311 | TTCGCCTTGTTGACC[A/G]GGCTGATCTCAAACT | 7110 |
rs116923973 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049329 | CAGTGAGCCATGATC[A/C]AACCACTGCACTTCA | 7110 |
rs116929134 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020751 | GTTTGAGTATCAGCT[A/G]TTTATTTGTAGATAA | 7110 |
rs117033224 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69025070 | TCAACAACTCATGTT[A/G]TTTCCTCCCATGTAC | 7110 |
rs117184929 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69045154 | TTAAAATATGACATA[C/T]TGCATTTAAAAAATA | 7110 |
rs117291761 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052435 | AACGCGGAAGGGTTT[A/C]TATTGATGTCGATTT | 7110 |
rs117799293 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69035639 | GGATATTCCCTACAG[C/T]ATTAAATAGGCTAGC | 7110 |
rs117855021 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | TMF1 | GRCh38.p7 | 3:69037088 | ATAAAAAGACAAACC[A/G]CCCAATTTAAAAATG | 7110 |
rs137901758 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69038423 | TAAAAAACACAACTG[G/T]TTAAATTTAGCAGAA | 7110 |
rs137951832 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TMF1 | GRCh38.p7 | 3:69026337 | CATGGTGGCTTATGC[C/T]TGTAATCCCAGCACT | 7110 |
rs137972720 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TMF1 | GRCh38.p7 | 3:69043367 | TAGAGATGAGGTCTC[A/G]CCATGTTGCCCAGGC | 7110 |
rs138022162 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69045031 | AGGGAGATGGATGCA[A/G]TCAAAAGAGGTCAAA | 7110 |
rs138150669 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052957 | GTTAGTGCCCTTATA[A/G]GAGAGGCCCAAGGGA | 7110 |
rs138189215 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053427 | CAGCCAGAGTGGTCA[A/C]CAAATAATTTTCACT | 7110 |
rs138457450 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024894 | AATCCAAAATGCTCA[A/G]TTGAGCTTTTCCTTT | 7110 |
rs138491199 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | TMF1 | GRCh38.p7 | 3:69031577 | GCAATGTGTACAAAG[C/G]ACCTTTCTATATTAT | 7110 |
rs138662785 | snp | A/G | 0.00914312 | 0.0669923 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053187 | TTATCCTAACAATGT[A/G]CACTGTGCATATTAC | 7110 |
rs138664980 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69043681 | CCAATATCAAAATAC[A/G]ATGAATGCACTCCTC | 7110 |
rs138710185 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TMF1 | GRCh38.p7 | 3:69024354 | ACAGTGGCAGAAAAA[C/T]GGTCCCAACTTTCCT | 7110 |
rs138887838 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | TMF1 | GRCh38.p7 | 3:69032095 | TCTAGACCAAATCTT[G/T]CATGGAACTCCAATT | 7110 |
rs138896543 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050419 | AAAATCAAAATTAAA[C/T]ATGCAAATGAACAAC | 7110 |
rs139325211 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69040063 | AATATCACCCAGATA[G/T]TTCCTACTAGAAATA | 7110 |
rs139402273 | in-del | -/AGAT | 0.0154538 | 0.0865337 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053862 | ATTTATTCAGCTCTC[-/AGAT]AGAGTCACCTTCTTA | 7110 |
rs139430861 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | TMF1 | GRCh38.p7 | 3:69046123 | CATTCATACATACAT[A/C]CATCCACACTAAAAG | 7110 |
rs139464017 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69027614 | TTTTGGTTCCCTGGG[C/T]CTCATTTGAAGAACA | 7110 |
rs139572312 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69034684 | ATGTTATAAATGACT[A/G]AAAATTAACAGAGGC | 7110 |
rs139694946 | snp | A/C | 0.00716266 | 0.059414 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020727 | TGTTTAACAATCAAA[A/C]TATGATCAGTTTGAG | 7110 |
rs139736121 | snp | A/G | 0.0152091 | 0.0858675 | intron-variant | TMF1 | GRCh38.p7 | 3:69028335 | AAAACAGAAAATGAA[A/G]AAGATGCTAGTATAG | 7110 |
rs139801478 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69034076 | CCTCAGCCTCCCAAA[A/G]CATTGGGATTATAGG | 7110 |
rs140028706 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69040776 | AAAATACAAAAACTA[C/G]CTAGGCGTGGTGGCA | 7110 |
rs140061964 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | TMF1 | GRCh38.p7 | 3:69045493 | AATAAATAAATAAAA[C/G]TAGAGGCCGGGCATG | 7110 |
rs140426277 | in-del | -/TG | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020668 | AGTTTTTCAAGAAAC[-/TG]TTTAAGTTCACTTTA | 7110 |
rs140452294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69030999 | TGGAATCAGCCTGGA[C/T]GTCCCTTGTGCAGTG | 7110 |
rs140558884 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69037197 | AACATCATTAGTCAT[A/T]AAGAGAATGCAAATC | 7110 |
rs140977386 | snp | A/C | 0.00358779 | 0.0422022 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69023020 | ATAATTTAACTGTAA[A/C]TATTACTACATAGTG | 7110 |
rs140994988 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69051319 | GTCCCTACTAAAAAT[A/G]CAAAAAGTTGCCGGG | 7110 |
rs141099261 | snp | A/C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052979 | CCCAAGGGAGCTCAC[A/C/G]GCAAGAAGGCACCAA | 7110 |
rs141161742 | snp | A/C/G | 0.000646027 | 0.0179612 | missense | TMF1 | GRCh38.p7 | 3:69033589 | AATTTCTCCCACGAC[A/C/G]ATGTCTGGGATCCCA | 7110 |
rs141231075 | snp | A/C | 0.00835141 | 0.0640778 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053231 | TTTTCTGTGTGCATT[A/C]TCTTCGAACATTTGG | 7110 |
rs141271498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039273 | GTATTAGGTTGGTGC[A/C]GTATTTTTAGCAGAG | 7110 |
rs141342323 | snp | C/T | 0.00358779 | 0.0422022 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022116 | ATTTGGAAGAAGGCA[C/T]AGCTACTTTTAAAAG | 7110 |
rs141404808 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | TMF1 | GRCh38.p7 | 3:69031718 | TTCTCCACCAAAGTA[A/G]AGCTAGTAATACCTC | 7110 |
rs141469416 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69036815 | TGTGAGAGCTAAGAC[C/T]ACAAAACTCTTAGAA | 7110 |
rs141566430 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019522 | CCGGATGTGCTGGTG[C/T]GCACCTGTAATCCCA | 7110 |
rs141609906 | in-del | -/AGTAATAGAGT | 0.452473 | 0.146644 | intron-variant | TMF1 | GRCh38.p7 | 3:69036012 | TATTTTATCTATCCC[-/AGTAATAGAGT]AGCAGAAACACAAAG | 7110 |
rs141674392 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69027010 | TATTTATTTTTATTT[C/T]TTTGAGAAAGAGTCT | 7110 |
rs142042513 | snp | C/T | 3.31208e-05 | 0.00406931 | missense | TMF1 | GRCh38.p7 | 3:69048329 | TTTTCACTTCTTCTT[C/T]TGGTCGTTGTGATTT | 7110 |
rs142108642 | snp | A/C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052340 | CAAATCTACGAGCCC[A/C/G]GAGTTCGGTCGACAG | 7110 |
rs142184606 | in-del | -/TTAT | 0.412917 | 0.189626 | intron-variant | TMF1 | GRCh38.p7 | 3:69024419 | CAGAGATAAATCCAA[-/TTAT]TTGTTTGAAAACATT | 7110 |
rs142338779 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69030212 | CTTTTCCAAAAGTAT[C/T]TTAATTTCAAAATGG | 7110 |
rs142512023 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69045123 | TATTATTCTTTACCC[A/G]AAACACATACCCTTT | 7110 |
rs142545095 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | TMF1 | GRCh38.p7 | 3:69047289 | TGCATCAATGAAAGT[A/G]TTTTTTAAAACAAAT | 7110 |
rs142584935 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049677 | GGTTTTTAAAAAAGC[A/G]CTACAAAGAAAATGA | 7110 |
rs142742731 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | TMF1 | GRCh38.p7 | 3:69037535 | TAATCCCAGCTACTC[A/G]GGAGGCTGAAGCAGG | 7110 |
rs142751419 | snp | C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69051178 | GGGAGTTGTTCTGAA[C/G]ATGAGAAGGCCATAA | 7110 |
rs142910144 | snp | A/T | 0.00716266 | 0.059414 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020729 | TTTAACAATCAAAAT[A/T]TGATCAGTTTGAGTA | 7110 |
rs142975245 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025141 | CTTCCCGGGGTAGCT[A/G]GAACAACTTATCTAA | 7110 |
rs143046655 | snp | G/T | | | missense | TMF1 | GRCh38.p7 | 3:69048397 | GTCTGGACATCAGTT[G/T]GCGAGAGAAAGGCAC | 7110 |
rs143141251 | in-del | -/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052879 | AACCTAATCTCCAAT[-/G]GGACAGTATTAAGGG | 7110 |
rs143222276 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019332 | AAGTAAATTCTTAGC[A/C]CTGTGTTTTCCGAAA | 7110 |
rs143430603 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052892 | ATGGGACAGTATTAA[C/G]GGGAGCCTTTAGGAG | 7110 |
rs143438137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69043550 | GGGCTCAAGTGATCC[A/G]CCCACTTCAGCCTCC | 7110 |
rs143550872 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TMF1 | GRCh38.p7 | 3:69041116 | CAAAATAATAACATT[C/T]GATATTAATATTTCA | 7110 |
rs143619008 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | TMF1 | GRCh38.p7 | 3:69045970 | ATTAGGTGGGAGGAC[C/T]GCTTGAGCCCAGGAG | 7110 |
rs143861047 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021400 | ATTCTGCCCTTGAAT[A/G]TTACACACACAAAAA | 7110 |
rs143957105 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69032573 | TAACATCACAGAAGG[A/G]CAACCTGGGGCATGA | 7110 |
rs144217851 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69035815 | AACTATAAAATAACA[C/T]GTAAGACATCAATTA | 7110 |
rs144284668 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | TMF1 | GRCh38.p7 | 3:69040280 | ATCCTGGGGCAGAAC[A/T]AATGATCAATTATAA | 7110 |
rs144703162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050654 | TAACTGGGGCACATA[C/T]GAAAAAACAGAGTTA | 7110 |
rs144820690 | snp | A/C | 0.00318978 | 0.0398085 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052989 | CTCACGGCAAGAAGG[A/C]ACCAACTCTAAGCCA | 7110 |
rs144854489 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69051496 | AACATAAAACCACAT[C/T]ACGCGCTACCAAGCG | 7110 |
rs144875999 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69042299 | CACCTCTGCCTCCCC[-/A]AGTGCTGAGATTACA | 7110 |
rs145127398 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69031862 | TGAGGGTATGTAGAC[C/T]TCAGTCTAAAAACCA | 7110 |
rs145161025 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | TMF1 | GRCh38.p7 | 3:69037087 | AATAAAAAGACAAAC[C/T]GCCCAATTTAAAAAT | 7110 |
rs145198215 | snp | G/T | 0.0360663 | 0.129354 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022150 | TTCTATGCTTTCCTT[G/T]TGTTTGAAATTTCAA | 7110 |
rs145259047 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | TMF1 | GRCh38.p7 | 3:69029530 | GCTCACTGCAACTTC[C/T]GCCTCCCGGGTGTAA | 7110 |
rs145379895 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69046955 | GTAAAAACAAATTCT[C/G]ATACAAGAAAAACCA | 7110 |
rs145488806 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052508 | CGATAGAGGTCGATT[A/T]CCCCGGAAGGAATAT | 7110 |
rs145770299 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TMF1 | GRCh38.p7 | 3:69035212 | TGTCAACATTGTTCA[C/T]GTATACTATTTCATA | 7110 |
rs145876700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69041599 | AGAAATAGTAAAACA[C/T]ATTATGGTATACCCA | 7110 |
rs145898813 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | TMF1 | GRCh38.p7 | 3:69024444 | GAAAACATTCAACCA[C/T]ATATTTTTCTAATCT | 7110 |
rs145992506 | snp | C/T | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050128 | AGGCAGGTGTGGTGA[C/T]GCAAACCTGCAATCC | 7110 |
rs146066743 | in-del | -/TAAA | 0.00914312 | 0.0669923 | intron-variant | TMF1 | GRCh38.p7 | 3:69031911 | GCATTCATTTATTGC[-/TAAA]TATTTATTTCAAAAG | 7110 |
rs146095995 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TMF1 | GRCh38.p7 | 3:69045183 | TAAAAGTAGGCCAGG[C/T]GCAGTGGCTCATGCC | 7110 |
rs146113769 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69025249 | GAGGAGGGATTCTCT[A/G]CTCCTAGATGCTTAT | 7110 |
rs146136734 | in-del | -/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69039767 | AATGTTTTATCTAAT[-/C]AGTAACATAAAAGAA | 7110 |
rs146216659 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020899 | ATCTTTTCTCTGCAA[A/G]TGAAGTTTTTTTCTA | 7110 |
rs146542987 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69036524 | GAACATGTAAGTATA[C/T]AGATACATATATTTT | 7110 |
rs146561067 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | TMF1 | GRCh38.p7 | 3:69040692 | AGCACTTTTGGGAAG[C/G]AGGCGGATCACCAGA | 7110 |
rs146941144 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | TMF1 | GRCh38.p7 | 3:69037683 | TGGTAGCACCTGCCT[A/G]TAGTCCCAGCTACTC | 7110 |
rs146957418 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69043335 | CCACCATGGCCAGCT[A/T]ATCTTTGTATTTTTT | 7110 |
rs147204297 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69034608 | TCATCCAAATATTTC[C/T]AAGTATTTATAAAAA | 7110 |
rs147330730 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | TMF1 | GRCh38.p7 | 3:69051218 | TTACAGGCTCGTGCC[C/T]GTAATCCCAGCACTT | 7110 |
rs147346094 | snp | C/T | 0.00256671 | 0.0357319 | missense | TMF1 | GRCh38.p7 | 3:69033682 | CTCAGTTCCTGGTTT[C/T]GATTCTCTGCTTCCT | 7110 |
rs147610295 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029654 | CCATGTTGGCCAGGC[C/T]GGTCTCCACCTCCTG | 7110 |
rs147698777 | snp | C/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022840 | TATAGATACAACTAG[C/T]TGTATATCTACAATA | 7110 |
rs147837782 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022085 | ACAACCTGGTTACCT[G/T]TTTGAATAAAATAAC | 7110 |
rs147926647 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052302 | TGTGCGCATGCGCTT[C/G]CTTCTTCCACGTACA | 7110 |
rs148191419 | snp | A/C/T | 0.000314684 | 0.0125398 | missense, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048479 | TTGCTTTAGGAGAGG[A/C/T]TATTGGTGGACTCTG | 7110 |
rs148383497 | snp | C/T | 0.0368353 | 0.130617 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019391 | TAGGGCCGGGCGCAG[C/T]GGCTTATGCCTATAA | 7110 |
rs148508066 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050728 | CATCACATACACACA[C/T]GGACCAAAATATCTT | 7110 |
rs148527377 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | TMF1 | GRCh38.p7 | 3:69035401 | GAGAAAAGACAGTGC[A/G]TCTATAAATATTTGC | 7110 |
rs148699796 | snp | A/C | 0.0123036 | 0.0774623 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021410 | TGAATATTACACACA[A/C]AAAAAAATCAAGCTG | 7110 |
rs148799360 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69037822 | AATATATATAAATTG[-/A]AAAAAAAAAATGCAA | 7110 |
rs149174901 | snp | G/T | 0.000928074 | 0.0215215 | missense | TMF1 | GRCh38.p7 | 3:69029900 | TTTCCTGTCTTAAAA[G/T]AGAATTCTGTGACTC | 7110 |
rs149320065 | snp | C/T | 0.00203735 | 0.0318516 | intron-variant | TMF1 | GRCh38.p7 | 3:69043728 | ATAGAGTTTAATTAA[C/T]ATTACTTTAAATTTC | 7110 |
rs149374059 | snp | G/T | 0.0126979 | 0.078662 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050486 | GATGACAGGAATTAA[G/T]TTTGCCTCTTGGAGA | 7110 |
rs149655876 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69028157 | TCTTGTTATCTCATT[A/G]ATTTGCTGCCATCCC | 7110 |
rs149691913 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052370 | GACGGAAGAACAGAA[C/G]AACGTTGACGTCACA | 7110 |
rs149709315 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69034966 | ACTGAGGAATTCTTT[C/T]ATTTCTAGAAAAACA | 7110 |
rs149714239 | snp | A/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69046303 | TTGGACTCAAAAAAA[A/T]AGTCTTACCTGAGTT | 7110 |
rs149884370 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021227 | AATAGAACTTTATCA[C/T]AGGTATATATGTATA | 7110 |
rs150060432 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | TMF1 | GRCh38.p7 | 3:69046600 | GAAGTCTATTAAAGA[C/T]ACCAGATCCAACTAA | 7110 |
rs150080864 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69043561 | ATCCGCCCACTTCAG[A/C]CTCCCAGTGTGCTGG | 7110 |
rs150201421 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69023621 | GATATAAAATTTAGT[C/G]TCTTTGTTCCATGGT | 7110 |
rs150297020 | in-del | -/G | 0.0379877 | 0.132479 | utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052277 | CACAGCTGAGACGAA[-/G]GGGGGCCCATGTGCG | 7110 |
rs150377249 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048872 | TTAAGGAAGTAACAG[C/T]ATATGTTTTATAACC | 7110 |
rs150431256 | snp | C/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053373 | AATCTAGATTTCCAG[C/G]TGCTTTTGAAAAATA | 7110 |
rs150766471 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69040039 | TCTGCTGATGTGATA[C/T]AGTTGTTCAATATCA | 7110 |
rs150820287 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69046093 | TAGCCTGGACAATAG[A/G]GAGAGACCCTGTCTC | 7110 |
rs150888177 | snp | A/G | 0.0162398 | 0.0886349 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020333 | ACTGTACAACTGGCA[A/G]TTCTCAAAAAATAGG | 7110 |
rs151086880 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | TMF1 | GRCh38.p7 | 3:69042091 | GCCCAGGCTGCAGTA[C/T]AGTGGCGTGATCTTG | 7110 |
rs151315406 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69037138 | TTAATTAATTTCTCC[C/G]AAGAAGATACATAAA | 7110 |
rs180717062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029007 | CAATGAATCCCAGTA[C/T]TATCTTCTTGTTATA | 7110 |
rs180740953 | snp | A/C | 0.02016 | 0.0983543 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021404 | TGCCCTTGAATATTA[A/C]ACACACAAAAAAATC | 7110 |
rs180741796 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69046760 | GACATTTCTCTTTCT[C/T]GTTCATGTGAAATAT | 7110 |
rs181271701 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69038164 | CCATCAACTGATGAT[A/T]TGATAAGACAAAGCC | 7110 |
rs181363789 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021046 | GCTTTCTGTGGTTTC[A/G]GTTACTCACGGTCAA | 7110 |
rs181367260 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69043233 | CTGGAGTAGTGGTAC[A/C]ATGACGACTCACCAC | 7110 |
rs181370734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025135 | CCCCTCCTTCCCGGG[A/G]TAGCTGGAACAACTT | 7110 |
rs181410543 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052503 | GCTACCGATAGAGGT[C/T]GATTTCCCCGGAAGG | 7110 |
rs181429838 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69034709 | AGAGGCATAGAAACC[A/G]GGAACTATTACCTGT | 7110 |
rs181511329 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69024904 | GCTCAATTGAGCTTT[A/T]CCTTTGAGCAGCATG | 7110 |
rs181626564 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69042739 | TTAGGAAGCATCAGC[C/T]AGTTATGTGGCAAGT | 7110 |
rs181843073 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69033963 | GGACTACAGGTACAC[A/G]CCACCACACCTGGCT | 7110 |
rs181964480 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69030333 | CATCACATCATTCAC[A/G]AAAATTAACTCAAAA | 7110 |
rs181972780 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | TMF1 | GRCh38.p7 | 3:69037310 | CCATCCTGGCTAACA[C/T]GCTGAAACCCCATGT | 7110 |
rs182086937 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69044345 | AAAAGAGAAAAGTAA[A/T]CTTTAGGGTTATAAT | 7110 |
rs182204791 | snp | A/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020688 | AAGTTCACTTTAACT[A/T]ACAGAAGTATTGAGA | 7110 |
rs182253596 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69047043 | GTAAGAAAATATTCC[C/T]TTCAAATTGACATAC | 7110 |
rs182383111 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69025854 | CACGTGTTTCCTCTC[A/C]CTAAAATTAGCACTC | 7110 |
rs182394678 | snp | A/C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69051774 | TTTCCCTCAGGAAAA[A/C/G]AGCAAAGACCGACTT | 7110 |
rs182458456 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031386 | TCTTGACTATGGTAA[C/T]GGATATGTGGTATAG | 7110 |
rs182646805 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69027033 | AAGAGTCTCGATCTG[C/T]TGCCCAGGCTGGAAT | 7110 |
rs182686443 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69045165 | CATATTGCATTTAAA[A/C]AATAAAAGTAGGCCA | 7110 |
rs182691241 | snp | A/C | 6.68125e-05 | 0.00577943 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69047922 | ACTTTCATGATCTAA[A/C]ACTTCAATATCACTG | 7110 |
rs182902900 | snp | A/G | 0.000198794 | 0.00996782 | missense | TMF1 | GRCh38.p7 | 3:69047636 | AATTAACTATAATAG[A/G]CACTAAAGCATATCC | 7110 |
rs182903083 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69030744 | AATGAGATATCACTA[C/T]ATGCTGTCTGAGTAA | 7110 |
rs182925169 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69036056 | TGGCATGACTTATAA[C/T]AGCAAAATACTGAAA | 7110 |
rs183128749 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053920 | AGCACCTATATGGTG[C/T]TAAATTTTAGTTCCT | 7110 |
rs183290665 | snp | C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026919 | TTTAAATTTACCTAT[C/G]GGTAGTTTAAATATA | 7110 |
rs183482179 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69040953 | TTTTTCTGGGGCACG[C/T]GGAAACAATATATAA | 7110 |
rs183519310 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69023756 | ATTGTGATGATACAT[A/G]TAACAACAATCAACA | 7110 |
rs183538983 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049150 | CAACACTAGAAGAGT[C/T]ATTTGAGTCCAGGAG | 7110 |
rs183545168 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69032713 | CTTCCCAGGTTCAAG[A/G]GATTCTTTGCCTCAG | 7110 |
rs183558948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69044858 | ATATCTAGTTGGGGA[C/T]CTACATACTCTTTGA | 7110 |
rs183567291 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69041348 | CTAAAGGACAGAGTG[G/T]CATACTTATTATTGT | 7110 |
rs183641280 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020351 | CTCAAAAAATAGGTA[A/G]AAGAAATGTAAGAAA | 7110 |
rs183679456 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69036844 | AAGAAAACTGATGAA[C/G]ATCTGCATAAACTTG | 7110 |
rs184176711 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039752 | CTAAAAATCTCAATA[G/T]AATGTTTTATCTAAT | 7110 |
rs184218506 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69033862 | TAGAAACGGGGTCCC[A/G]CTCTGTCACCCAGGC | 7110 |
rs184334135 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69028936 | AGGTACAAATCCTTT[C/T]CCTGGAAAAAAAAAT | 7110 |
rs184380350 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69045647 | TAGCCAGGCATGGTA[G/T]CATACGTCTGTAGTC | 7110 |
rs184409179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051180 | GAGTTGTTCTGAAGA[C/T]GAGAAGGCCATAAAA | 7110 |
rs184452275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69028127 | GTTCCAAAAGCAGTG[G/T]CATCACCCATTTCAT | 7110 |
rs184522265 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69027320 | TCATTTCAGAAAAAT[C/T]ACCCTCATTAACCAG | 7110 |
rs184566440 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69033209 | AACCTGGGAGGCGGA[A/G]CTTGCAGTGAGCCGA | 7110 |
rs184595794 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024990 | CAAACCTGTAAAACA[C/T]TTCAATATTTCTGAC | 7110 |
rs184601560 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050129 | GGCAGGTGTGGTGAC[A/G]CAAACCTGCAATCCC | 7110 |
rs185037466 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TMF1 | GRCh38.p7 | 3:69036468 | TGTAAAAAGGATGTA[A/G]GAGACAGAAATAGGT | 7110 |
rs185108560 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69037343 | ACTAAAAATACAAAA[A/C]AAAATTAGCAGGGTG | 7110 |
rs185184767 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TMF1 | GRCh38.p7 | 3:69046274 | AGTATAAAAGGAGTA[A/G]GAAGGGTTCCTTTTT | 7110 |
rs185224026 | snp | C/T | 5.01006e-05 | 0.00500478 | intron-variant | TMF1 | GRCh38.p7 | 3:69042763 | GGCAAGTACTTTTCC[C/T]GTTCTTACAGTATTT | 7110 |
rs185251199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69044087 | AAAATCTGTTAGAAA[A/G]AGAAAATGTCACCAA | 7110 |
rs185257531 | snp | A/G | 0.000265107 | 0.0115101 | missense | TMF1 | GRCh38.p7 | 3:69025630 | ATTATGCTTGATCCT[A/G]CTCCCATCCTTACAG | 7110 |
rs185312468 | snp | A/G | 0.00120874 | 0.0245542 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69047655 | TAAAGCATATCCCTT[A/G]CCTGACAATTCATCA | 7110 |
rs185397792 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69039360 | GCCTGTCGCAGCCTC[C/T]GAAAGTGTTGGGATT | 7110 |
rs185403266 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021519 | ATTTATTAACACTAC[C/T]AATCAGAGATCCAAT | 7110 |
rs185749329 | snp | A/G | 0.00172415 | 0.0293105 | missense | TMF1 | GRCh38.p7 | 3:69024072 | TTAGCTGAGTTCTAA[A/G]TTTGGGTATCTCCTT | 7110 |
rs185799883 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69030355 | AACTCAAAATGGATC[A/G]TAGACTTATATGTAA | 7110 |
rs185842953 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69047244 | AGAAATGGCAAAATG[C/T]GTATGTTTTTAAATC | 7110 |
rs185881973 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69041903 | AGAGAAATAAAAAGA[A/G]AGATTCACTTGACCA | 7110 |
rs185922706 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69035502 | ATACATTATAAACTA[A/C]CATAGCCTTTTTGGA | 7110 |
rs185942585 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053653 | TCTAACTACAGTAAA[A/C]ACTTGCATGTTAAAA | 7110 |
rs186045462 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69046776 | GTTCATGTGAAATAT[A/G]GCTATCAATAGGAGA | 7110 |
rs186047424 | snp | A/G | | | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054244 | AACATGGTCAGGCAT[A/G]GTGGCTCATGCCTGT | 7110 |
rs186081443 | snp | G/T | 0.0275645 | 0.114116 | utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052279 | ACAGCTGAGACGAAG[G/T]GGGCCCATGTGCGCA | 7110 |
rs186135684 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029469 | TTTTTTTTTGAGACC[A/G]AGTCTCACTCTGTCA | 7110 |
rs186177500 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021170 | CTGTTATAATTGTTC[C/T]ATTTGCAGTTATTGT | 7110 |
rs186202187 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69031018 | CCTTGTGCAGTGAAT[C/G]GTTAAATATACGTGG | 7110 |
rs186303906 | snp | A/G | 0.000265878 | 0.0115268 | intron-variant | TMF1 | GRCh38.p7 | 3:69038747 | AGATTGAGTTTATAA[A/G]TGTTGCCAGTGATCA | 7110 |
rs186646645 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TMF1 | GRCh38.p7 | 3:69027089 | CAGCCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT | 7110 |
rs186648148 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69045184 | AAAAGTAGGCCAGGC[A/G]CAGTGGCTCATGCCT | 7110 |
rs186746018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69023848 | AGTTCTTTTCCTATA[C/T]TGGGACTAAACATGA | 7110 |
rs186775089 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69041391 | ATCTGACATACTAAC[C/T]GTTCAATAAATATTA | 7110 |
rs186847076 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022704 | ACTTTAACACTTAAT[A/G]TACATTTTCATGAGC | 7110 |
rs186872672 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020822 | TAGAAATTGTTAATA[C/T]GGATAAAAAAAGAAT | 7110 |
rs186888901 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69040954 | TTTTCTGGGGCACGC[A/G]GAAACAATATATAAT | 7110 |
rs186990498 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69025910 | CCATAGAATGGCAAG[G/T]TCATGATGACAGACA | 7110 |
rs187068002 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69034817 | CTATCATAACATTAT[C/T]TTCTATAAAACAAAA | 7110 |
rs187225189 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69044360 | TCTTTAGGGTTATAA[C/T]TGAAAGCTATACAAC | 7110 |
rs187443063 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | TMF1 | GRCh38.p7 | 3:69026980 | TTCAATACAGAAAAC[C/T]CATTTTTATTTATTT | 7110 |
rs187475515 | snp | C/G/T | 0.00953873 | 0.0683987 | intron-variant | TMF1 | GRCh38.p7 | 3:69044953 | ACATGTATAAGAATA[C/G/T]TTTATGTAGCTTCCT | 7110 |
rs187503657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69032901 | CAGGTGTGAGCCACC[A/G]CGCCCTGCCAGAATA | 7110 |
rs187680274 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048699 | TGCACCTGCTAAACT[C/T]CTTGCTTACTACATC | 7110 |
rs187720478 | snp | A/T | 0.0103295 | 0.0711199 | intron-variant | TMF1 | GRCh38.p7 | 3:69035756 | AATTACAATAAATGT[A/T]TAAAACATGTAAAAA | 7110 |
rs187982307 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031974 | AGCACATTGCTCTCA[A/G]AAGCTGTCAGAGATA | 7110 |
rs188141233 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019639 | CCCAGGCAACAGAGT[A/G]AGACTCTGTCAAAAA | 7110 |
rs188331820 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69039946 | TACTAATTTTAAAGA[A/G]AAAAATCTGGCAGTC | 7110 |
rs188556044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69043093 | CAACTTTGAAAATGA[C/T]ATTCAAAACCTAAAT | 7110 |
rs188568544 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025133 | TACCCCTCCTTCCCG[C/G]GGTAGCTGGAACAAC | 7110 |
rs188619024 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021788 | CAGGTTCAAGCAATG[C/G]TCCTGCCTCAGCCTC | 7110 |
rs188651563 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027782 | TGGGCCACATGCCAA[A/C]CAGGGCCACAGGTTG | 7110 |
rs188683027 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69046539 | AAATTAAGTAATTCA[A/G]TACATGGCACTTACA | 7110 |
rs188760580 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69036433 | GTTATAAAACAGTGT[A/G]AATAATAAACTGTCA | 7110 |
rs188908405 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69046205 | AAAGCTAAACAAAAA[G/T]TAATGCTTGGAATGT | 7110 |
rs189181148 | snp | C/T | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020549 | TCATTTTCCTATCCA[C/T]TAAAATATAAATATT | 7110 |
rs189206096 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69046288 | AGGAAGGGTTCCTTT[C/T]TGGACTCAAAAAAAT | 7110 |
rs189211810 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TMF1 | GRCh38.p7 | 3:69028526 | TTTATTTATTGGTGC[C/T]CTGGGTTAAGATTTC | 7110 |
rs189228226 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69037216 | AGAATGCAAATCAGC[C/T]GGGCGTAGTGGCTCA | 7110 |
rs189347758 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69051383 | GGGAGGCTGGGGAAG[A/G]AGAATCGCTAGAACC | 7110 |
rs189366185 | snp | A/G | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052501 | TGGCTACCGATAGAG[A/G]TCGATTTCCCCGGAA | 7110 |
rs189369951 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TMF1 | GRCh38.p7 | 3:69034298 | GCCAACATGGTGAAA[A/C]CTCATCTCTACTAAA | 7110 |
rs189434253 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69033298 | AAAAAAAAAAGAACT[G/T]AATGAAAGAATGACA | 7110 |
rs189586055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69033921 | CTGTAGCCTCAACCT[A/C]CTAGGCTCAAGCGAT | 7110 |
rs189591645 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | TMF1 | GRCh38.p7 | 3:69036667 | ATAGATTTTGCTCTC[A/G]CTTTGGAATCATGTA | 7110 |
rs189738017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050354 | ATGTAGAAAACTTCA[C/G]TTTGGAGGCATAGTT | 7110 |
rs189855306 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029000 | TACATGACAATGAAT[C/T]CCAGTACTATCTTCT | 7110 |
rs190004919 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69044121 | CTGACATGTAAAAAT[A/C]AGAGAAGAGTAAATA | 7110 |
rs190012116 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | TMF1 | GRCh38.p7 | 3:69027014 | TATTTTTATTTTTTT[G/T]AGAAAGAGTCTCGAT | 7110 |
rs190026936 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69035575 | CCTTTCACCGGGCCA[C/T]CCTAGTCTTGGGAAT | 7110 |
rs190056169 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TMF1 | GRCh38.p7 | 3:69045049 | AAAAGAGGTCAAAGA[A/G]GAAATTTAAAGCCTC | 7110 |
rs190158791 | snp | C/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020886 | GAGTTTTATTGCAAT[C/G]TTTTCTCTGCAAATG | 7110 |
rs190263070 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69029721 | GCTGGGATTACAGGC[A/G]TGAGCCACGGCGCCC | 7110 |
rs190278169 | snp | A/C/T | 0.000218511 | 0.0104503 | intron-variant | TMF1 | GRCh38.p7 | 3:69038795 | TTCTTCAACATCCTA[A/C/T]TCTGATAATTCATTC | 7110 |
rs190292451 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021296 | GTTTCAGACGTTCAC[C/T]GGGGGTCTTGGAACG | 7110 |
rs190403839 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | TMF1 | GRCh38.p7 | 3:69038142 | AAAGTATAAATAACC[C/T]ATATGCCCATCAACT | 7110 |
rs190404728 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69042367 | TAAATCTTTTCAGAG[A/T]CAAAAGTGCTTAATA | 7110 |
rs190551525 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TMF1 | GRCh38.p7 | 3:69046813 | AAATAACATAAGCAG[A/G]AAACAAACTGAAGCA | 7110 |
rs190658887 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024897 | CCAAAATGCTCAATT[C/G]AGCTTTTCCTTTGAG | 7110 |
rs190692431 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69030593 | TAGTATCAGGAATAT[A/G]TAACAATCTAGTTAG | 7110 |
rs190694509 | snp | C/T | 0.000399281 | 0.0141238 | missense | TMF1 | GRCh38.p7 | 3:69047479 | GAAGAAACCAAGATA[C/T]CAGGCTGTTCACAGT | 7110 |
rs190937555 | snp | G/T | 1.70151e-05 | 0.00291672 | intron-variant | TMF1 | GRCh38.p7 | 3:69025756 | TACTCAGTTATCATA[G/T]CTTGTCTTCCATTAC | 7110 |
rs190938833 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039381 | TGTTGGGATTACAGG[A/C]GTGAGCCACCCCACT | 7110 |
rs190950136 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021646 | CTATATTCTGAAGTA[C/G]TAGTGTTTTAATTTT | 7110 |
rs190964085 | snp | A/G | 0.0142736 | 0.0832652 | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054289 | GGGAAGCCGAGGGGG[A/G]CGGGGGGGGGTGGAT | 7110 |
rs191093651 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69034861 | TGTATAATTTTTAAG[A/G]TGCCCACTCTGATTT | 7110 |
rs191096695 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69019837 | CACTATTACTATTTT[A/G]AAATCTTTATTCAAT | 7110 |
rs191131337 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69036688 | GAATCATGTAAATGT[G/T]TTACACATACAAAAC | 7110 |
rs191239433 | snp | A/T | 0.00633916 | 0.055941 | missense | TMF1 | GRCh38.p7 | 3:69047777 | CAGTGAGTTTTTGGA[A/T]ATCATCTAAACGATT | 7110 |
rs191736719 | snp | A/G | 0.00159617 | 0.0282053 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022762 | ATGTGAAAGATTTCA[A/G]AGTTTCAGTATGTTA | 7110 |
rs191745417 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69046357 | ACTTACCTTCTTAAA[A/T]ACACTGAAATTCAAA | 7110 |
rs191772420 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022379 | TATAGGGTAGTAAAA[C/T]AATACTTCTTCAAAA | 7110 |
rs191783197 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69041093 | TCTCTGACAAAATTA[C/T]TAAATTACAAAATAA | 7110 |
rs191961774 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050030 | TTTGGGAGGCCGAGG[C/T]GGGCGGACCACCTGA | 7110 |
rs191964252 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032983 | CCTTAGACCTATTTT[C/T]GCTCTTGGAATTCTA | 7110 |
rs192018090 | snp | A/G | 0.00341885 | 0.0412036 | intron-variant | TMF1 | GRCh38.p7 | 3:69044627 | CATAAAAGTCAGAAC[A/G]CTTAGCTTTAAAAAA | 7110 |
rs192068551 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TMF1 | GRCh38.p7 | 3:69039966 | ATCTGGCAGTCAACT[A/C]CTTAACTAAGCATTC | 7110 |
rs192156892 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027120 | CCCACCTCTGCCTCC[C/T]GAGTAGCTGGGATTA | 7110 |
rs192329917 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69026572 | TGGCGGTGAGCTGAG[A/T]TAGCACCACTACACT | 7110 |
rs192458422 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69041430 | AATGAAAAAGTTGGA[G/T]AAAGCTAACTTTCAA | 7110 |
rs192537198 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69045288 | CACGGTGAAAACCAG[C/T]CTCTACTGAAAATAC | 7110 |
rs192566093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69035928 | GGTAACTCATATATG[C/G]TCTATCTCCCATTCC | 7110 |
rs192648539 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69036463 | ATTTATGTAAAAAGG[A/G]TGTAGGAGACAGAAA | 7110 |
rs192762507 | snp | C/T | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050574 | ACTATGGGCATTTTC[C/T]GAAAACAAATATCCT | 7110 |
rs192950746 | snp | C/T | 0.00261494 | 0.0360643 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69033585 | CTCTAATTTCTCCCA[C/T]GACGATGTCTGGGAT | 7110 |
rs193073047 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | TMF1 | GRCh38.p7 | 3:69032012 | GACCTAACATTTATA[C/T]CTATAAATTTAAATA | 7110 |
rs193118119 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69046260 | TGGTGATAAACTTGA[C/G]TATAAAAGGAGTAGG | 7110 |
rs193237879 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049113 | TGAACTCAGTGGGTA[G/T]GGAGGTTCACACCTA | 7110 |
rs193275199 | snp | C/T | 0.00255324 | 0.0356385 | intron-variant | TMF1 | GRCh38.p7 | 3:69027881 | TACACCACAAACAAA[C/T]AAAAACAAAATTCAA | 7110 |
rs199517973 | snp | A/G | 0.000232717 | 0.0107844 | missense | TMF1 | GRCh38.p7 | 3:69038937 | GATCTTTCTCTTGGC[A/G]TTCTACCATGGAATT | 7110 |
rs199525986 | snp | A/G | 0.000182641 | 0.00955443 | missense | TMF1 | GRCh38.p7 | 3:69026094 | CAGAAAATGGCTTGC[A/G]TTCCTTAGGGAGTAA | 7110 |
rs199639236 | snp | C/T | 0.0028628 | 0.0377254 | intron-variant | TMF1 | GRCh38.p7 | 3:69044626 | ACATAAAAGTCAGAA[C/T]GCTTAGCTTTAAAAA | 7110 |
rs199770568 | snp | C/G | 6.81745e-05 | 0.00583803 | intron-variant | TMF1 | GRCh38.p7 | 3:69025757 | ACTCAGTTATCATAG[C/G]TTGTCTTCCATTACC | 7110 |
rs199805291 | snp | A/G | 6.66067e-05 | 0.00577052 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69048033 | AGGTTCCAAAGCTAT[A/G]TCCTTTGTTTCTGCT | 7110 |
rs199993661 | snp | A/T | 0.000199352 | 0.0099818 | intron-variant | TMF1 | GRCh38.p7 | 3:69033709 | TCCTGGAGTCTCTGA[A/T]TCATGAAATTCTGAA | 7110 |
rs200074443 | snp | C/T | 1.68502e-05 | 0.00290255 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69043801 | AACTTTCTTTTCTGC[C/T]TCTGCAATTCTTTGA | 7110 |
rs200147058 | snp | A/G/T | 0.00220461 | 0.0331281 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69047766 | ACAGCAACTCTCAGT[A/G/T]AGTTTTTGGAAATCA | 7110 |
rs200159475 | snp | A/G | 0.00014904 | 0.00863121 | missense | TMF1 | GRCh38.p7 | 3:69035075 | TCCTTTCTGGCAGCC[A/G]CTTGTTCTGTACGCT | 7110 |
rs200175993 | snp | A/G | 1.65658e-05 | 0.00287795 | missense, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048481 | GCTTTAGGAGAGGCT[A/G]TTGGTGGACTCTGAG | 7110 |
rs200270972 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024269 | TTAATGTGTGTGTGG[G/T]TTTTTTTTTTTTTTT | 7110 |
rs200301053 | snp | G/T | 0.00094594 | 0.0217273 | missense | TMF1 | GRCh38.p7 | 3:69048089 | ATATACTTTCCATAG[G/T]TGTTTTCACATCAAT | 7110 |
rs200330868 | snp | A/T | 4.99988e-05 | 0.00499969 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69029985 | TCTCTCAACTGCTGC[A/T]GCCAGCAAGGTCTGG | 7110 |
rs200396777 | snp | A/G | 0.000133143 | 0.00815803 | missense | TMF1 | GRCh38.p7 | 3:69047821 | GCAGATGCAGAGAGA[A/G]GCTGAAAAGATGTCT | 7110 |
rs200412103 | snp | A/C | 6.30669e-05 | 0.00561511 | missense | TMF1 | GRCh38.p7 | 3:69027989 | ACTGACTATTCAACA[A/C]TGTCTAATAGAGAGA | 7110 |
rs200424101 | snp | A/G | 1.70148e-05 | 0.00291669 | intron-variant | TMF1 | GRCh38.p7 | 3:69044613 | GGATAAGGCGAATAC[A/G]TAAAAGTCAGAACGC | 7110 |
rs200527724 | snp | A/G | 0.000399281 | 0.0141238 | missense | TMF1 | GRCh38.p7 | 3:69025594 | CCTTCCCTTAGCTTT[A/G]GCTGAGACTGTAGGT | 7110 |
rs200595469 | snp | C/T | 0.000100277 | 0.00708016 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69047409 | CTGACTTTCAGCAGG[C/T]TCACACTGCTCAGCC | 7110 |
rs200601497 | in-del | -/ATT | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024418 | ACAGAGATAAATCCA[-/ATT]ATTTGTTTGAAAACA | 7110 |
rs200769311 | snp | A/G | 0.000399281 | 0.0141238 | stop-gained | TMF1 | GRCh38.p7 | 3:69038868 | TATCCAGGGCAGCCT[A/G]AATACTTCGGTTCTT | 7110 |
rs200775188 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69028941 | AAATCCTTTCCCTGG[-/A]AAAAAAAAATAAATA | 7110 |
rs200894146 | snp | A/C/T | 0.000120653 | 0.00776608 | intron-variant | TMF1 | GRCh38.p7 | 3:69030027 | TTACAGGACAGAAAA[A/C/T]AAAATCACATACACA | 7110 |
rs200959132 | snp | A/C/G | 0.000113477 | 0.00753177 | intron-variant | TMF1 | GRCh38.p7 | 3:69039028 | TATGTTATAAAAACA[A/C/G]ACAAAAGTATTTTTC | 7110 |
rs201147126 | snp | A/G | 4.98699e-05 | 0.00499324 | missense | TMF1 | GRCh38.p7 | 3:69048067 | AGAGACTGCGTAGAC[A/G]TATTAGATATACTTT | 7110 |
rs201166573 | snp | A/G/T | 0.0001584 | 0.00889814 | missense | TMF1 | GRCh38.p7 | 3:69023182 | TTTTCACAAGTTAAC[A/G/T]GAGACTTTGTCTTAA | 7110 |
rs201210501 | snp | A/T | 6.62899e-05 | 0.00575678 | missense | TMF1 | GRCh38.p7 | 3:69042863 | AAAAGGTCTGCAGTT[A/T]CACTACTATTTAATC | 7110 |
rs201235194 | in-del | -/TT | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024269 | TTAATGTGTGTGTGG[-/TT]TTTTTTTTTTTTTTG | 7110 |
rs201252682 | snp | A/C/G | 0.00031489 | 0.012544 | missense, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048496 | ATTGGTGGACTCTGA[A/C/G]GTTCAGTGTTTGATT | 7110 |
rs201326000 | snp | A/G | 4.96824e-05 | 0.00498385 | missense | TMF1 | GRCh38.p7 | 3:69048229 | AGAGTTTCCCCTGAA[A/G]CACACAAAGAAGAGT | 7110 |
rs201345267 | snp | C/G/T | 0.000530376 | 0.0162762 | missense | TMF1 | GRCh38.p7 | 3:69029930 | CCATGGAAGACATCT[C/G/T]AATTTTGTTAGCAAG | 7110 |
rs201356844 | snp | G/T | 0.000217699 | 0.0104308 | missense | TMF1 | GRCh38.p7 | 3:69052065 | CGAAGCTGGAGAGCT[G/T]GGAGGCGTTGAACCA | 7110 |
rs201366322 | snp | C/T | 0.00051445 | 0.01603 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038926 | AAGACGGCCAAGATC[C/T]TTCTCTTGGCGTTCT | 7110 |
rs201384518 | in-del | -/A | 0.0236746 | 0.106192 | intron-variant | TMF1 | GRCh38.p7 | 3:69026767 | TCTGTTAAGCTTCAT[-/A]ATTATACAATATACT | 7110 |
rs201388840 | snp | C/T | 1.65622e-05 | 0.00287764 | missense | TMF1 | GRCh38.p7 | 3:69047522 | CACTTCGTCCACTTT[C/T]TTCCATTTCTGCTTC | 7110 |
rs201445607 | snp | C/T | 0.000203338 | 0.0100811 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69024058 | AAGAATACTTACTCT[C/T]AGCTGAGTTCTAAGT | 7110 |
rs201489178 | snp | A/C | 1.66927e-05 | 0.00288895 | stop-gained | TMF1 | GRCh38.p7 | 3:69044517 | TATCAAAAGCTTCTT[A/C]TAGAAGTGCTTTTTC | 7110 |
rs201513097 | snp | A/C/G | 4.97082e-05 | 0.00498518 | missense, stop-gained | TMF1 | GRCh38.p7 | 3:69038590 | ATGTTTCTTGCTGCT[A/C/G]ACGGGCTTCTTCTTG | 7110 |
rs201740646 | snp | A/G | 0.000438271 | 0.0147967 | intron-variant | TMF1 | GRCh38.p7 | 3:69039505 | CCAACTGTTCATACA[A/G]GAAGTAATAACAATA | 7110 |
rs201746420 | snp | C/T | 0.000480367 | 0.0154904 | missense | TMF1 | GRCh38.p7 | 3:69048173 | TATTAACAGTTTCTT[C/T]GTGCTTGCCTTCAGT | 7110 |
rs201798874 | snp | A/C | 0.00042183 | 0.0145168 | missense | TMF1 | GRCh38.p7 | 3:69023184 | TTCACAAGTTAACTG[A/C]GACTTTGTCTTAAAA | 7110 |
rs201799457 | snp | A/G | 0.000779416 | 0.0197256 | intron-variant | TMF1 | GRCh38.p7 | 3:69028214 | GAGCTGAGTGGTCAC[A/G]AAGAGAAATACCTTT | 7110 |
rs201931170 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029048 | CTTTATTTATTTTTT[-/A]TTTTTTTGGAGACGG | 7110 |
rs201961736 | snp | A/T | 0.000236859 | 0.0108799 | intron-variant | TMF1 | GRCh38.p7 | 3:69033533 | TGCATCGAGCATAAA[A/T]ACTAAAGCAGTTACC | 7110 |
rs202050225 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | TMF1 | GRCh38.p7 | 3:69031437 | ACACACACACACACA[A/G]ACACAAATGAGTACC | 7110 |
rs202061947 | snp | A/G | 0.000274024 | 0.011702 | synonymous-codon, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048552 | TCCTCCACTGACAGG[A/G]GAACTTATTCCTTTA | 7110 |
rs202102186 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029043 | TATTTTTTTTTTTTT[-/T]GGAGACGGAGTCTCG | 7110 |
rs202131403 | in-del | -/TTC | | | intron-variant | TMF1 | GRCh38.p7 | 3:69042528 | TGACAGGCTCTTAAG[-/TTC]ACCTGTTTAAAGTTT | 7110 |
rs202166071 | snp | C/G | 1.68315e-05 | 0.00290094 | missense | TMF1 | GRCh38.p7 | 3:69043805 | TTCTTTTCTGCTTCT[C/G]CAATTCTTTGAGTAA | 7110 |
rs202168999 | snp | G/T | 0.00199792 | 0.0315431 | synonymous-codon, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048507 | CTGAGGTTCAGTGTT[G/T]GATTTCAACCCCCAG | 7110 |
rs202228261 | snp | A/C | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69054094 | CAAAAAACATTTGAA[A/C]AGAAAACTGCCATAT | 7110 |
rs202240773 | snp | C/G | 8.33535e-05 | 0.00645521 | missense | TMF1 | GRCh38.p7 | 3:69048011 | TGTCTTCATGTTTTT[C/G]TTCCTTAGGTTCCAA | 7110 |
rs367564184 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69030569 | AAATGCAAACCATAT[A/G]TCTAGGATTAGTATC | 7110 |
rs367577890 | snp | A/G | 3.3123e-05 | 0.00406945 | missense | TMF1 | GRCh38.p7 | 3:69035088 | CCGCTTGTTCTGTAC[A/G]CTGCAATGCAAGCCT | 7110 |
rs367745212 | snp | A/G | | | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048767 | AGAAAACTGGTGTGG[A/G]TCCACCTGAGAGGAA | 7110 |
rs367785816 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026354 | GTAATCCCAGCACTT[-/T]GGGAGGCCAAGGAGG | 7110 |
rs367796742 | snp | A/G | 1.89081e-05 | 0.00307468 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69023312 | AGTGTTGTACCTTTG[A/G]TCCAAATCCTGAAAA | 7110 |
rs367844847 | snp | A/C/G | 3.31665e-05 | 0.00407215 | missense | TMF1 | GRCh38.p7 | 3:69029945 | GAATTTTGTTAGCAA[A/C/G]GAGTTCTTCTGTAGC | 7110 |
rs367941967 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029056 | TATTTTTTTTTTTTT[G/T]GAGACGGAGTCTCGC | 7110 |
rs367951399 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050313 | TAAATATATGTATGA[C/T]TTCAAAGGCAGTTAG | 7110 |
rs368048047 | in-del | -/AAC | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69054100 | CATTTGAACAGAAAA[-/AAC]CTGCCATATCTAAGT | 7110 |
rs368078848 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69025887 | CCACAAGTATTCAGA[G/T]GAATTACCCATAGAA | 7110 |
rs368107014 | snp | G/T | 3.416e-05 | 0.00413265 | intron-variant | TMF1 | GRCh38.p7 | 3:69043882 | GAACATTTCACTAAA[G/T]TTAAAATAATATTTG | 7110 |
rs368110416 | snp | C/T | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053045 | AATCTGCCGGCTCCT[C/T]ATCTTGGACTTCTCA | 7110 |
rs368124720 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034035 | GCTCAGGCTGGCCTC[A/G]AACTCCTGAGCAGGC | 7110 |
rs368198729 | snp | A/T | 1.76002e-05 | 0.00296644 | intron-variant | TMF1 | GRCh38.p7 | 3:69030040 | AAAAAAATCACATAC[A/T]CATACAGCCCAGAGA | 7110 |
rs368216364 | snp | A/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69044697 | AACAGCTTTATCTCA[A/T]AAAAACAATCAAGAA | 7110 |
rs368236966 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69023504 | AAAAAGGAATTAAAG[-/A]AAAAAAACCAAGCTA | 7110 |
rs368243438 | snp | C/T | 0.000133402 | 0.00816599 | missense | TMF1 | GRCh38.p7 | 3:69047867 | TTGATTTTGAATCTG[C/T]AGTCTCTTGTCTCGA | 7110 |
rs368281160 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69040632 | CTCTTTAGCTTTAAG[-/T]TTTAAAAATACTGGC | 7110 |
rs368344372 | snp | A/T | 3.31219e-05 | 0.00406938 | missense | TMF1 | GRCh38.p7 | 3:69035063 | CGTAAATAATCCTCC[A/T]TTCTGGCAGCCGCTT | 7110 |
rs368348342 | snp | C/T | 0.000134312 | 0.00819376 | missense | TMF1 | GRCh38.p7 | 3:69052071 | TGGAGAGCTGGGAGG[C/T]GTTGAACCAACTCAT | 7110 |
rs368403333 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024847 | GGAATAATTGCATTA[C/T]GTACTTACTGGTTGA | 7110 |
rs368647187 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69029286 | TGATCCACCTGCCTC[A/C]GCCTCCCAAAGTGCT | 7110 |
rs368670523 | snp | C/T | 6.76601e-05 | 0.00581597 | intron-variant | TMF1 | GRCh38.p7 | 3:69044606 | ACTGTCTGGATAAGG[C/T]GAATACATAAAAGTC | 7110 |
rs368738500 | snp | A/C | 0.000166005 | 0.00910907 | missense | TMF1 | GRCh38.p7 | 3:69038891 | CGGTTCTTTTCTTCA[A/C]GTTCATCCATGTCTA | 7110 |
rs368743439 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029463 | TATTTTTTTTTTTTT[A/G]AGACCGAGTCTCACT | 7110 |
rs368760241 | snp | A/G | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050360 | AAAACTTCAGTTTGG[A/G]GGCATAGTTCTACAC | 7110 |
rs368806459 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69041589 | GTACAACACTAGAAA[C/T]AGTAAAACATATTAT | 7110 |
rs368825200 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019695 | TAATAATGTAACTTA[C/T]AGAAAATTAGGGCTT | 7110 |
rs368894111 | snp | G/T | 0.000141295 | 0.00840403 | missense | TMF1 | GRCh38.p7 | 3:69023227 | GAGTTTTGTACATAT[G/T]TTTTACATCTTCGAG | 7110 |
rs368967805 | snp | A/G | 0.000167986 | 0.00916322 | missense | TMF1 | GRCh38.p7 | 3:69039606 | TTTTTGTTCAGCTTT[A/G]CAACCATATTTTCAT | 7110 |
rs368969818 | snp | G/T | 1.7095e-05 | 0.00292356 | intron-variant | TMF1 | GRCh38.p7 | 3:69024226 | TCAAAACATATCTTT[G/T]TTAATACTCCCAGTA | 7110 |
rs369047770 | snp | A/G | 3.31235e-05 | 0.00406948 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038660 | CATTTCACGGCTCAG[A/G]GCAGCTTCCTGTGCC | 7110 |
rs369123106 | in-del | -/AAAA | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034884 | CTGATTTATTCACAC[-/AAAA]AAGCCACAAAAATTC | 7110 |
rs369248756 | snp | A/C | 1.66687e-05 | 0.00288688 | missense | TMF1 | GRCh38.p7 | 3:69047415 | TTCAGCAGGTTCACA[A/C]TGCTCAGCCACCTTG | 7110 |
rs369280643 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69036533 | AGTATATAGATACAT[A/G]TATTTTCTTGCATTT | 7110 |
rs369282446 | snp | C/T | 0.000115958 | 0.00761352 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038600 | CTGCTGACGGGCTTC[C/T]TCTTGGGCCTTCTCT | 7110 |
rs369303236 | snp | C/T | 1.65781e-05 | 0.00287902 | missense | TMF1 | GRCh38.p7 | 3:69048148 | GTTGGCACCTTCATA[C/T]CCGATTCTTTATTAA | 7110 |
rs369394218 | snp | C/T | 4.96964e-05 | 0.00498455 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69033603 | CGATGTCTGGGATCC[C/T]AGGGTTGCTTGCAAA | 7110 |
rs369422334 | snp | C/G | | | utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052192 | TTTTCCACTCGGCTG[C/G]TTCTGTCAGCGTGTG | 7110 |
rs369504266 | snp | C/T | 1.65647e-05 | 0.00287786 | missense | TMF1 | GRCh38.p7 | 3:69048190 | TGCTTGCCTTCAGTT[C/T]TAGGTGATGAAGTAC | 7110 |
rs369571405 | snp | C/T | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020637 | AATATTCAATAGGTA[C/T]TCTGCCACCTACTGG | 7110 |
rs369588729 | snp | C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69028439 | AGTGATTTTCCAACA[C/G]TGTGTTCCAGATCCC | 7110 |
rs369774520 | snp | A/G | 1.65603e-05 | 0.00287747 | stop-gained | TMF1 | GRCh38.p7 | 3:69048335 | CTTCTTCTTCTGGTC[A/G]TTGTGATTTTGCTGG | 7110 |
rs369799154 | snp | C/T | 3.3129e-05 | 0.00406982 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69033645 | TCGAAGCAATGGTCT[C/T]GTTGTTGATGAAACA | 7110 |
rs369841938 | snp | C/T | 4.98583e-05 | 0.00499266 | intron-variant | TMF1 | GRCh38.p7 | 3:69039546 | GAATTATGATTGCTA[C/T]TCACCTGTTTCAAAT | 7110 |
rs369885696 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026715 | CATTTATTACAACAA[C/T]GTAATTTGTTGGGTT | 7110 |
rs369987060 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051379 | ACTAGGGAGGCTGGG[A/G]AAGGAGAATCGCTAG | 7110 |
rs369992241 | snp | A/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69042387 | AGTGCTTAATAATTT[A/C]AAAATTAATACAATG | 7110 |
rs370063861 | snp | A/C/T | 4.97503e-05 | 0.00498729 | missense | TMF1 | GRCh38.p7 | 3:69029890 | AATCTACTGTTTTCC[A/C/T]GTCTTAAAAGAGAAT | 7110 |
rs370138830 | snp | C/T | 5.02163e-05 | 0.00501055 | missense | TMF1 | GRCh38.p7 | 3:69024074 | AGCTGAGTTCTAAGT[C/T]TGGGTATCTCCTTCA | 7110 |
rs370152473 | snp | C/T | 8.39666e-05 | 0.00647891 | missense | TMF1 | GRCh38.p7 | 3:69043812 | CTGCTTCTGCAATTC[C/T]TTGAGTAAACTCATC | 7110 |
rs370183559 | snp | C/G | 1.6599e-05 | 0.00288084 | splice-donor-variant | TMF1 | GRCh38.p7 | 3:69025995 | AAAAATAAAACATCA[C/G]CTGAGACAGAAAAGA | 7110 |
rs370191688 | snp | A/G | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020857 | AATTTTATAAAATTG[A/G]AAAGTTTAGGAATGA | 7110 |
rs370247528 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032785 | CAGCTGATTTTTGTA[C/T]TTTTGGTAGAGACGG | 7110 |
rs370339846 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031933 | TTATTTCAAAAGATA[C/T]CATTTTCAGATGTCT | 7110 |
rs370413821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048886 | GTATATGTTTTATAA[C/T]CCACAGTAAGTCCAA | 7110 |
rs370426365 | snp | C/T | 3.31472e-05 | 0.00407093 | missense, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048493 | GCTATTGGTGGACTC[C/T]GAGGTTCAGTGTTTG | 7110 |
rs370550590 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052869 | CCTATGTTGAAACCT[A/C]ATCTCCAATGGGACA | 7110 |
rs370563862 | snp | C/T | 1.66095e-05 | 0.00288175 | intron-variant | TMF1 | GRCh38.p7 | 3:69038736 | CTTAAAAAATTAGAT[C/T]GAGTTTATAAATGTT | 7110 |
rs370605608 | snp | C/T | 0.000264936 | 0.0115064 | missense | TMF1 | GRCh38.p7 | 3:69048448 | TCGACCACAGTCCTC[C/T]GAACTGGCTTTGTGA | 7110 |
rs370623550 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69043266 | CCTCAACCTCCCAGG[C/G]TCAGGTGATCCTCCC | 7110 |
rs370663671 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69029505 | GCTGGAGTGCAGTGG[A/T]GGGATCTTGGCTCAC | 7110 |
rs370672075 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024747 | TGTATTGTGTTTAAC[A/G]CTGAAAAGAGGTATC | 7110 |
rs370672484 | snp | A/G | 3.31664e-05 | 0.00407211 | missense | TMF1 | GRCh38.p7 | 3:69029948 | TTTTGTTAGCAAGGA[A/G]TTCTTCTGTAGCTGC | 7110 |
rs370706471 | snp | C/T | 8.29359e-05 | 0.00643903 | missense | TMF1 | GRCh38.p7 | 3:69025676 | TTCCATTTGCTGATA[C/T]AGGCATTGGTCCAAA | 7110 |
rs370826273 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69033746 | ACCAATGACAGCAAT[A/G]AAAACATTAAAAACA | 7110 |
rs370837315 | snp | C/T | 1.67959e-05 | 0.00289787 | intron-variant | TMF1 | GRCh38.p7 | 3:69038815 | ATAATTCATTCTAAA[C/T]GGGTTGCATATTTGT | 7110 |
rs370861218 | snp | C/T | 5.14884e-05 | 0.00507362 | missense | TMF1 | GRCh38.p7 | 3:69029828 | ACCTATTGTTCTCAT[C/T]CTCCAGTTTACACAG | 7110 |
rs370878356 | snp | C/T | 5.38662e-05 | 0.00518943 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048602 | AAAAGAACACATATA[C/T]GTTACATTAATATTT | 7110 |
rs370882998 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69027138 | GTAGCTGGGATTACA[A/G]GCACATGCCACCATG | 7110 |
rs370935349 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032984 | CTTAGACCTATTTTC[A/G]CTCTTGGAATTCTAC | 7110 |
rs371034299 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69037404 | AAGCACTTTGGGAGG[C/T]GGAGGCGGGTGGATC | 7110 |
rs371071815 | snp | C/T | 0.000331746 | 0.0128749 | intron-variant | TMF1 | GRCh38.p7 | 3:69042798 | TAGTCAACCAAATAC[C/T]ATACGCACCTTCTTC | 7110 |
rs371091215 | snp | C/T | 8.29717e-05 | 0.00644042 | missense | TMF1 | GRCh38.p7 | 3:69038915 | ATGTCTACCTGAAGA[C/T]GGCCAAGATCTTTCT | 7110 |
rs371093589 | snp | A/G | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053997 | TTATAAATTTATTCC[A/G]TATGGTTTTATAATA | 7110 |
rs371149868 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052363 | GTCGACAGACGGAAG[A/G]ACAGAAGAACGTTGA | 7110 |
rs371228024 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69044944 | CACTAGGCGACATGT[A/G]TAAGAATACTTTATG | 7110 |
rs371337662 | snp | G/T | 1.65669e-05 | 0.00287805 | missense | TMF1 | GRCh38.p7 | 3:69047623 | TTTGGAGTTGAAGAA[G/T]TAACTATAATAGGCA | 7110 |
rs371444244 | snp | A/C | 1.69424e-05 | 0.00291048 | intron-variant | TMF1 | GRCh38.p7 | 3:69025746 | TTCACACAGTTACTC[A/C]GTTATCATAGCTTGT | 7110 |
rs371495070 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034522 | GCTTCTTTAAAAAGC[A/G]TTTCTAAGATAGTCT | 7110 |
rs371579994 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69024530 | AAAAATATACTTTAA[C/T]GTAGCCCCACCTGTG | 7110 |
rs371685358 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69039204 | AATTTTCGTGCCTTA[A/G]CCTCCCAAGTAGCTG | 7110 |
rs371732478 | snp | C/G | 4.96948e-05 | 0.00498447 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038606 | ACGGGCTTCTTCTTG[C/G]GCCTTCTCTAATGCT | 7110 |
rs371744049 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69045229 | TTGGGAGGCTGAGGT[G/T]GGGGGATCACCTGAG | 7110 |
rs371748724 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69040706 | GCAGGCGGATCACCA[C/G]AGGTCAGGAGTTCAA | 7110 |
rs371751751 | snp | C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034521 | TGCTTCTTTAAAAAG[C/G]GTTTCTAAGATAGTC | 7110 |
rs371833369 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050443 | GAACAACCAAGATTA[C/T]GTCTGATTAATTTAA | 7110 |
rs371851702 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029058 | TTTTTTTTTTTTTGG[A/G]GACGGAGTCTCGCTC | 7110 |
rs372062081 | snp | A/T | 0.000370146 | 0.0135991 | intron-variant | TMF1 | GRCh38.p7 | 3:69039508 | ACTGTTCATACAGGA[A/T]GTAATAACAATATAT | 7110 |
rs372078206 | snp | A/G | 3.314e-05 | 0.00407049 | missense | TMF1 | GRCh38.p7 | 3:69033592 | TTCTCCCACGACGAT[A/G]TCTGGGATCCCAGGG | 7110 |
rs372218765 | snp | A/G | 0.000169985 | 0.00921758 | intron-variant | TMF1 | GRCh38.p7 | 3:69043916 | ATGAGGATGGTGTCT[A/G]TATATCCCAAAGGTA | 7110 |
rs372262056 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69029683 | TGACCTCAAGTGATC[C/T]GCCCGCCTTGGCCTC | 7110 |
rs372379885 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69043421 | GCGATCCACCCTCTT[C/T]GGCCTCCTGAGTAGC | 7110 |
rs372397563 | snp | A/C/G/T | 0.000156851 | 0.00885473 | intron-variant | TMF1 | GRCh38.p7 | 3:69033504 | TAATTCTATAAACAA[A/C/G/T]ATGGAAGAGCTTCTG | 7110 |
rs372459337 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048809 | TGGTAGTCCAGGCCA[G/T]GCCCAGTCTTTTGTC | 7110 |
rs372549076 | in-del | -/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024802 | AATGTTTCAAATTTC[-/T]TTTTTTTTTTTTTTT | 7110 |
rs372551913 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69027375 | CTTAAGTGCCTATAG[A/G]CCAAATGATGTGCAC | 7110 |
rs372561090 | snp | C/G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053408 | TACCAAGCATGGGAA[C/G/T]AGTCAGCCAGAGTGG | 7110 |
rs372584488 | snp | A/C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69033386 | AGAGACATAATAAAG[A/C/G]TATTAAAAATACATG | 7110 |
rs372632754 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024927 | GCAGCATGTCAGCAC[G/T]CAAAGTTTTGGATTT | 7110 |
rs372654258 | snp | C/T | 0.000167986 | 0.00916323 | missense | TMF1 | GRCh38.p7 | 3:69038694 | CTATCCTTTGCAGCA[C/T]TGGCTTTGTGAAGAT | 7110 |
rs372712074 | snp | C/T | 4.6856e-05 | 0.00484002 | intron-variant | TMF1 | GRCh38.p7 | 3:69028029 | AGACAATTTCTGTGA[C/T]AGTAATTCATGCCAT | 7110 |
rs372738397 | snp | A/C | 0.000136542 | 0.0082615 | utr-variant-5-prime | TMF1 | GRCh38.p7 | 3:69052100 | ATCGCCCCTCCTCAG[A/C]CGGCAGTGGCGGCGG | 7110 |
rs372895906 | snp | C/T | 4.98708e-05 | 0.00499328 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69048066 | GAGAGACTGCGTAGA[C/T]GTATTAGATATACTT | 7110 |
rs372940990 | snp | C/T | 0.000232789 | 0.0107861 | intron-variant | TMF1 | GRCh38.p7 | 3:69029777 | TGCTTTAGGATGTCA[C/T]GGAACTACCAAAAAT | 7110 |
rs373012784 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048686 | AATACCTGTAATTTG[C/T]ACCTGCTAAACTCCT | 7110 |
rs373123669 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032629 | TTTTTTTTTTTTTTT[G/T]AGATGCAGTCTCGCT | 7110 |
rs373173107 | snp | A/G | 1.65611e-05 | 0.00287755 | missense | TMF1 | GRCh38.p7 | 3:69048238 | CCTGAAACACACAAA[A/G]AAGAGTCTTTTACTT | 7110 |
rs373194763 | snp | A/G | 4.97442e-05 | 0.00498695 | intron-variant | TMF1 | GRCh38.p7 | 3:69042803 | AACCAAATACTATAC[A/G]CACCTTCTTCCATTA | 7110 |
rs373195117 | snp | C/T | 0.000169986 | 0.00921759 | missense | TMF1 | GRCh38.p7 | 3:69033622 | GTTGCTTGCAAATTT[C/T]CTATTTGTCGAAGCA | 7110 |
rs373314601 | snp | C/T | 1.66087e-05 | 0.00288168 | missense | TMF1 | GRCh38.p7 | 3:69029870 | CTGATTCTAGCTGGG[C/T]TTGAAATCTACTGTT | 7110 |
rs373359359 | snp | C/G | 5.45608e-05 | 0.00522278 | intron-variant | TMF1 | GRCh38.p7 | 3:69047337 | GCACATCTAAAAATC[C/G]CTTCCACTTACTAGA | 7110 |
rs373454566 | in-del | -/TT | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026197 | AACAAAGATTCAGTC[-/TT]TTAAAAAAGCCACAC | 7110 |
rs373469918 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032363 | ACAGAATACCCTGAG[C/T]CCATGTCTCCTGACT | 7110 |
rs373504008 | snp | A/G | 3.31516e-05 | 0.0040712 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69033678 | TTGACTCAGTTCCTG[A/G]TTTCGATTCTCTGCT | 7110 |
rs373517771 | snp | C/T | 1.74873e-05 | 0.00295691 | intron-variant | TMF1 | GRCh38.p7 | 3:69025521 | TATTAGGCCTCAAAA[C/T]TTCATTTACTTCTAT | 7110 |
rs373525616 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69043422 | CGATCCACCCTCTTC[G/T]GCCTCCTGAGTAGCT | 7110 |
rs373538352 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69046702 | TTTCACATGTATTAG[A/G]TAGAAGCAATCTGTC | 7110 |
rs373570693 | snp | A/G | 4.96816e-05 | 0.00498381 | missense | TMF1 | GRCh38.p7 | 3:69048400 | TGGACATCAGTTGGC[A/G]AGAGAAAGGCACTGA | 7110 |
rs373677617 | snp | A/G | 1.77934e-05 | 0.00298268 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69023282 | TTCTGCTTTTTCTCC[A/G]TACATCTGCAGAATA | 7110 |
rs373685720 | snp | C/T | 0.000165986 | 0.00910854 | missense | TMF1 | GRCh38.p7 | 3:69047698 | TCACTTACACTCCGG[C/T]TATCTAATGACTGTA | 7110 |
rs373685880 | snp | A/G | 4.97839e-05 | 0.00498893 | missense | TMF1 | GRCh38.p7 | 3:69038916 | TGTCTACCTGAAGAC[A/G]GCCAAGATCTTTCTC | 7110 |
rs373845110 | snp | G/T | 1.65734e-05 | 0.00287862 | missense, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048494 | CTATTGGTGGACTCT[G/T]AGGTTCAGTGTTTGA | 7110 |
rs373885968 | snp | A/C/G | 9.93849e-05 | 0.0070487 | missense | TMF1 | GRCh38.p7 | 3:69026027 | GTCTGTAGTCCTGCC[A/C/G]TATCAACACCACTTA | 7110 |
rs373935145 | snp | A/T | 1.67607e-05 | 0.00289483 | missense | TMF1 | GRCh38.p7 | 3:69043826 | CTTTGAGTAAACTCA[A/T]CTTTCAAGGAAGAAA | 7110 |
rs373996552 | snp | C/G | 1.65861e-05 | 0.00287972 | missense | TMF1 | GRCh38.p7 | 3:69039557 | GCTATTCACCTGTTT[C/G]AAATGCTGCAACTCC | 7110 |
rs374027843 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031951 | TTTTCAGATGTCTCA[C/T]ATTTCACAGCACATT | 7110 |
rs374210616 | snp | A/C/G | 1.65682e-05 | 0.00287817 | missense, synonymous-codon | TMF1 | GRCh38.p7 | 3:69048174 | ATTAACAGTTTCTTC[A/C/G]TGCTTGCCTTCAGTT | 7110 |
rs374212079 | in-del | -/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024802 | GAATGTTTCAAATTT[-/C]TTTTTTTTTTTTTTT | 7110 |
rs374275300 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69024540 | TTTAACGTAGCCCCA[C/T]CTGTGTAGGTTGTAT | 7110 |
rs374312951 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | TMF1 | GRCh38.p7 | 3:69037754 | GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCACTG | 7110 |
rs374384387 | snp | C/G | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022770 | GATTTCAAAGTTTCA[C/G]TATGTTAACATTACT | 7110 |
rs374424268 | snp | C/T | 1.76213e-05 | 0.00296822 | missense | TMF1 | GRCh38.p7 | 3:69023224 | TTTGAGTTTTGTACA[C/T]ATTTTTTACATCTTC | 7110 |
rs374456194 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029165 | CAGCCTCCCGAGTAG[C/T]TGGAATTACAGGCGT | 7110 |
rs374546747 | snp | C/T | 1.65943e-05 | 0.00288043 | intron-variant | TMF1 | GRCh38.p7 | 3:69034982 | ATTTCTAGAAAAACA[C/T]ATACTTCTTGGATTT | 7110 |
rs374604731 | snp | G/T | 3.31807e-05 | 0.00407299 | missense | TMF1 | GRCh38.p7 | 3:69024157 | CATTATTGATCGAGT[G/T]TTTTCTAGATTGCCA | 7110 |
rs374606709 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029464 | ATTTTTTTTTTTTTG[A/G]GACCGAGTCTCACTC | 7110 |
rs374637515 | snp | A/G | 0.000147902 | 0.00859819 | intron-variant | TMF1 | GRCh38.p7 | 3:69043705 | ACTCCTCAAAAATCT[A/G]TATCTCTATAGAGTT | 7110 |
rs374638924 | snp | A/G | 0.000167986 | 0.00916323 | intron-variant | TMF1 | GRCh38.p7 | 3:69025750 | CACAGTTACTCAGTT[A/G]TCATAGCTTGTCTTC | 7110 |
rs374741223 | snp | G/T | 4.96841e-05 | 0.00498393 | missense | TMF1 | GRCh38.p7 | 3:69035079 | TTCTGGCAGCCGCTT[G/T]TTCTGTACGCTGCAA | 7110 |
rs374845313 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029462 | TTATTTTTTTTTTTT[G/T]GAGACCGAGTCTCAC | 7110 |
rs374853679 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69038315 | CTCTTCTCTTCTAAG[A/G]GGGTTCCTAGCTTTT | 7110 |
rs374864262 | snp | A/G | 1.65888e-05 | 0.00287996 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69048125 | TTTCAGATACTTTCA[A/G]ACTTACAGTTGGCAC | 7110 |
rs374966234 | snp | A/G | 5.04359e-05 | 0.00502149 | missense | TMF1 | GRCh38.p7 | 3:69038963 | GAATTTAGTTTTTTA[A/G]TATTTTCTCTATGTT | 7110 |
rs374966644 | snp | A/G | | | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048653 | TATAAATATAAATTT[A/G]GAAAAAATACCCTAT | 7110 |
rs375037050 | snp | C/T | 0.000198304 | 0.00995555 | intron-variant | TMF1 | GRCh38.p7 | 3:69023366 | AATAACTACACAGAA[C/T]ATCTTTAATATTTAT | 7110 |
rs375093435 | snp | A/T | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021489 | TTTTATGAATCTGGC[A/T]CACACTGAAAGAATA | 7110 |
rs375124442 | snp | C/T | 1.65638e-05 | 0.00287778 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038618 | TTGGGCCTTCTCTAA[C/T]GCTGCAGAAAGTTCT | 7110 |
rs375151342 | snp | C/G | 5.0407e-05 | 0.00502006 | missense | TMF1 | GRCh38.p7 | 3:69028264 | GTGTTCTTACATATT[C/G]ATCTTTTAGGTTTTC | 7110 |
rs375300466 | snp | C/T | 0.000169986 | 0.00921759 | missense | TMF1 | GRCh38.p7 | 3:69033595 | TCCCACGACGATGTC[C/T]GGGATCCCAGGGTTG | 7110 |
rs375395667 | snp | C/T | 0.00139928 | 0.0264136 | missense | TMF1 | GRCh38.p7 | 3:69038865 | CACTATCCAGGGCAG[C/T]CTGAATACTTCGGTT | 7110 |
rs375446737 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69043493 | GTATTTTTTAGTAGA[A/G]GCAGGGTCTCACCAT | 7110 |
rs375586664 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69037606 | GAGATTGCGCTATTG[C/T]ACTCCAGCCTGGGCA | 7110 |
rs375591364 | snp | A/C/T | 9.93685e-05 | 0.00704812 | missense | TMF1 | GRCh38.p7 | 3:69035048 | TCACCGATCTCATGG[A/C/T]GTAAATAATCCTCCT | 7110 |
rs375612774 | snp | C/G/T | 4.98213e-05 | 0.00499085 | synonymous-codon, missense | TMF1 | GRCh38.p7 | 3:69052009 | CTGGATGTCCAGAAC[C/G/T]CTGTCAATAGACTTC | 7110 |
rs375651787 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69040395 | ACTATGATGTACCTG[G/T]CAAGGAAAACGTACT | 7110 |
rs375672154 | in-del | -/TCA | | | intron-variant | TMF1 | GRCh38.p7 | 3:69036185 | TTACTAGAGTGATCA[-/TCA]GGATATTTTACTAAG | 7110 |
rs375751485 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032631 | TTTTTTTTTTTTTGA[A/G]ATGCAGTCTCGCTCT | 7110 |
rs375813869 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69037220 | TGCAAATCAGCCGGG[C/T]GTAGTGGCTCACGCC | 7110 |
rs376034890 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69036053 | CCATGGCATGACTTA[C/T]AATAGCAAAATACTG | 7110 |
rs376039606 | snp | A/G/T | 4.97594e-05 | 0.00498775 | missense | TMF1 | GRCh38.p7 | 3:69038569 | CATTGCTTACTTGAA[A/G/T]GGCTAATGTTTCTTG | 7110 |
rs376124326 | snp | C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69040731 | GTTCAAGACCAGCCT[C/G]GCCAACATGGTGAAA | 7110 |
rs376295784 | snp | A/G | 1.65605e-05 | 0.0028775 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69048285 | AGGAGTTCTTGACTG[A/G]CCAATGTGCAAGGAT | 7110 |
rs376310069 | snp | A/G | | | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048950 | TACTTATCAATATGA[A/G]ATAAACTAATATGGA | 7110 |
rs376365644 | snp | A/G | 1.65641e-05 | 0.00287781 | missense | TMF1 | GRCh38.p7 | 3:69033641 | TTTGTCGAAGCAATG[A/G]TCTTGTTGTTGATGA | 7110 |
rs376423508 | snp | A/C/T | 8.30244e-05 | 0.00644254 | missense | TMF1 | GRCh38.p7 | 3:69027929 | TTTCTTGAGTAAAAA[A/C/T]GGCTTTCTTCCTTTC | 7110 |
rs376477050 | snp | C/T | 1.65674e-05 | 0.00287809 | missense | TMF1 | GRCh38.p7 | 3:69047639 | TAACTATAATAGGCA[C/T]TAAAGCATATCCCTT | 7110 |
rs376558880 | snp | C/T | 0.000167986 | 0.00916322 | missense | TMF1 | GRCh38.p7 | 3:69039594 | AGCTCTTTAACTTTT[C/T]TGTTCAGCTTTGCAA | 7110 |
rs376560893 | snp | C/T | 1.65908e-05 | 0.00288012 | missense | TMF1 | GRCh38.p7 | 3:69024159 | TTATTGATCGAGTTT[C/T]TTCTAGATTGCCAAT | 7110 |
rs376647086 | snp | G/T | 1.66704e-05 | 0.00288703 | intron-variant | TMF1 | GRCh38.p7 | 3:69039538 | TATGTAGAGAATTAT[G/T]ATTGCTATTCACCTG | 7110 |
rs376962471 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69037361 | AATTAGCAGGGTGGC[C/T]GGGCATGGTGGCTCA | 7110 |
rs376963978 | snp | A/T | 1.65619e-05 | 0.00287762 | missense | TMF1 | GRCh38.p7 | 3:69038658 | TTCATTTCACGGCTC[A/T]GAGCAGCTTCCTGTG | 7110 |
rs377093434 | snp | A/C | 0.0158469 | 0.0875917 | intron-variant | TMF1 | GRCh38.p7 | 3:69027617 | TGGTTCCCTGGGCCT[A/C]ATTTGAAGAACAAGA | 7110 |
rs377176964 | snp | C/T | 0.000215401 | 0.0103757 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69025632 | TATGCTTGATCCTGC[C/T]CCCATCCTTACAGCA | 7110 |
rs377178920 | snp | G/T | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052482 | CTTAGCGAAGGGGAA[G/T]CTATGGCTACCGATA | 7110 |
rs377191532 | snp | A/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69030827 | CACATTACTCTTACA[A/C]AGCCACTTTGTAAAC | 7110 |
rs377250483 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026824 | AAAATTACTAATGAG[C/T]GTTACAAATCATAAA | 7110 |
rs377257341 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69047120 | GATGTAAGATGAAAA[A/C]TTTCATGCTTAACTG | 7110 |
rs377288950 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048748 | TAATACAGGGACTTA[C/T]GGAAGAAAACTGGTG | 7110 |
rs377334887 | snp | A/G | 0.000298526 | 0.0122137 | intron-variant | TMF1 | GRCh38.p7 | 3:69029807 | TATCACTCAGAAACC[A/G]TGCTCACCTATTGTT | 7110 |
rs377392623 | snp | C/T | 0.000169986 | 0.00921759 | missense | TMF1 | GRCh38.p7 | 3:69042855 | TCTCTTTCAAAAGGT[C/T]TGCAGTTTCACTACT | 7110 |
rs377447363 | snp | C/T | 0.000331351 | 0.0128672 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038699 | CTTTGCAGCATTGGC[C/T]TTGTGAAGATCAGTA | 7110 |
rs377540805 | snp | A/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029631 | TTTTTAGGAGAGAGT[A/C]GGTTTCGCCATGTTG | 7110 |
rs377563526 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69043450 | GCTGTGACCACAGGC[A/G]CACACCAGCATGACC | 7110 |
rs377564520 | snp | A/G | 0.000183387 | 0.00957391 | intron-variant | TMF1 | GRCh38.p7 | 3:69042775 | TCCTGTTCTTACAGT[A/G]TTTTTCATAGTCAAC | 7110 |
rs377565518 | snp | A/G | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021984 | CCACAGCACCTGGCC[A/G]TAAATGAGAGTTTTT | 7110 |
rs377641345 | snp | A/T | 1.66479e-05 | 0.00288508 | intron-variant | TMF1 | GRCh38.p7 | 3:69038759 | TAAATGTTGCCAGTG[A/T]TCAGATAATAGAAAA | 7110 |
rs386396968 | in-del | -/T | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021692 | AGAGTTTGTTTTTTT[-/T]TTTTTTGAGACGGAG | 7110 |
rs397727281 | in-del | -/AA | | | intron-variant | TMF1 | GRCh38.p7 | 3:69046304 | GGACTCAAAAAAATA[-/AA]GTCTTACCTGAGTTT | 7110 |
rs397801328 | in-del | -/AT/CA | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031436 | ACACACACACACACA[-/AT/CA]TACACAAATGAGTAC | 7110 |
rs397990000 | in-del | -/T | 0 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69028725 | GGAAGAACAGAGGGT[-/T]AAAAAATACTAACCA | 7110 |
rs397990001 | in-del | -/T | 0 | 0 | intron-variant | TMF1 | GRCh38.p7 | 3:69032628 | TTTTTTTTTTTTTTT[-/T]GAGATGCAGTCTCGC | 7110 |
rs527427541 | in-del | -/A | 0.0111196 | 0.0737302 | intron-variant | TMF1 | GRCh38.p7 | 3:69024796 | GACCAGGAATGTTTC[-/A]AATTTCTTTTTTTTT | 7110 |
rs527443185 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026179 | TTTCCTAGGGTTAAT[A/G]AGAACAAAGATTCAG | 7110 |
rs527820153 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021725 | TTTCTCTGTCACCCA[G/T]GCTGGAGTGCAGTGG | 7110 |
rs527848437 | snp | A/C/G | 8.34907e-05 | 0.00646062 | missense | TMF1 | GRCh38.p7 | 3:69047881 | GTAGTCTCTTGTCTC[A/C/G]AGCTCGCTGAGCTCT | 7110 |
rs527966093 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69041920 | GATTCACTTGACCAC[A/G]TTTTCCAAAGGCTCC | 7110 |
rs528021600 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69035715 | ATAGTTGCAAATGTC[A/G]ATACAACATGAATAT | 7110 |
rs528160839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037362 | ATTAGCAGGGTGGCC[A/G]GGCATGGTGGCTCAT | 7110 |
rs528197622 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69044969 | TTTATGTAGCTTCCT[A/G]GTAATAGCAAAAATC | 7110 |
rs528245007 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69030120 | CCACACTTAAAACTG[A/G]TAACTATTTATTGCC | 7110 |
rs528367378 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049676 | GGGTTTTTAAAAAAG[C/T]GCTACAAAGAAAATG | 7110 |
rs528510786 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051336 | AAAAAGTTGCCGGGC[A/G]TGGTGGTGGGCGCCT | 7110 |
rs528573756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69051688 | ACCAACCAACCAAGT[C/T]CCCTGTCATCCAAGT | 7110 |
rs528695543 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69031070 | CAGCAATAAAAAGAC[A/T]AAACTACCGATACAA | 7110 |
rs528728450 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69030192 | CTTATACCTGCTTTA[C/T]CACTCTTTTCCAAAA | 7110 |
rs528746933 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024252 | CAGTAATATAAAAAT[A/G]TTTAATGTGTGTGTG | 7110 |
rs528901842 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69042125 | CACTGCAACCTCCAC[C/G]TCCCAGGCTCAAGCA | 7110 |
rs528902757 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049526 | TCTCTAAATCCCACT[A/C/T]TCCAAGCCCACTCTA | 7110 |
rs529106566 | in-del | -/CT | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052729 | GATCACGTATGAACA[-/CT]GTGTCCAACTCGTGG | 7110 |
rs529547006 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022082 | AACACAACCTGGTTA[C/T]CTTTTTGAATAAAAT | 7110 |
rs529580926 | snp | A/T | 8.75572e-05 | 0.00661596 | intron-variant | TMF1 | GRCh38.p7 | 3:69030036 | AGAAAAAAAAATCAC[A/T]TACACATACAGCCCA | 7110 |
rs529784455 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69029638 | GAGAGAGTAGGTTTC[A/G]CCATGTTGGCCAGGC | 7110 |
rs529868022 | snp | C/T | 1.66261e-05 | 0.00288319 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69044563 | TAACTGAGCCTCCCT[C/T]TTTTCCAGCTTTTCA | 7110 |
rs529871711 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051260 | GGTGGGTGGATCGCC[A/T]TAAGTCAGGAGTTCC | 7110 |
rs529921686 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037925 | TCTTGGCAAGGATGT[A/G]GAGAAACTGAAACCC | 7110 |
rs529983439 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69031357 | GGACTCAATAGTGTT[A/G]GAACTGTTCAATATC | 7110 |
rs530005528 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69045920 | AAAAAATAGCCAGGC[A/G]TGGTGCGAGCCTATG | 7110 |
rs530031331 | snp | G/T | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049550 | CACTCTAAGAGGAAG[G/T]TTTGTTCTCAAATTC | 7110 |
rs530063582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039294 | TTTAGCAGAGACAGG[A/G]TTTCGCCTTGTTGAC | 7110 |
rs530132169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69046489 | TTTGTTTGTGAATAT[C/T]TAACCTGATTAACAG | 7110 |
rs530196560 | snp | C/T | 0.00089438 | 0.0211279 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69039599 | TTTAACTTTTTTGTT[C/T]AGCTTTGCAACCATA | 7110 |
rs530326880 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052478 | AGTTCTTAGCGAAGG[A/G]GAAGCTATGGCTACC | 7110 |
rs530429640 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037761 | CAGTGAGCTGAGATC[A/G]TGCCACTGTGCTCCA | 7110 |
rs530567515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024335 | TCTTTCTTAAGTAAA[C/G]GAAACAGTGGCAGAA | 7110 |
rs530684331 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049857 | TTCAAATTAAAATGT[C/G]GCTGAACAAAATATT | 7110 |
rs530696080 | snp | A/G | 1.74509e-05 | 0.00295384 | intron-variant | TMF1 | GRCh38.p7 | 3:69043918 | GAGGATGGTGTCTAT[A/G]TATCCCAAAGGTATA | 7110 |
rs530851773 | in-del | -/AG | | | intron-variant | TMF1 | GRCh38.p7 | 3:69041900 | ACAAGAGAAATAAAA[-/AG]AGAGATTCACTTGAC | 7110 |
rs531007410 | snp | C/T | 1.66098e-05 | 0.00288177 | intron-variant | TMF1 | GRCh38.p7 | 3:69038735 | TCTTAAAAAATTAGA[C/T]TGAGTTTATAAATGT | 7110 |
rs531013114 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69045802 | CACGGGTTCATGCTT[A/G]TAATCCCAGCACTGT | 7110 |
rs531052978 | snp | C/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69036836 | ACTCTTAGAAGAAAA[C/G]TGATGAAGATCTGCA | 7110 |
rs531069187 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039234 | GGGACTACAGATGTG[C/T]ACCACCACGCCCGGC | 7110 |
rs531086732 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034244 | TTGGGAGGCTGAGGT[G/T]GGTGGATCACCTGAA | 7110 |
rs531464323 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025948 | CATTTGCATATTTCC[C/T]TTATTATTATTCTAA | 7110 |
rs531540554 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69032936 | ATCTTAAGACTCCCT[A/G]GTATGTCTCTTCTAA | 7110 |
rs531572515 | snp | C/T | 1.76347e-05 | 0.00296935 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69023249 | ATCTTCGAGATCTAA[C/T]CGAAGTTCTTCTGCC | 7110 |
rs531602160 | snp | C/G | 0.000380911 | 0.0137953 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69035113 | AAGCCTAAGGTCCCC[C/G]ACCTGTAGGAGGAGA | 7110 |
rs531603380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69033454 | ACAAAATGTAACTAT[C/T]AGATCAAATGAATTT | 7110 |
rs531627792 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027255 | CCTACCTCAGCCTCT[C/G]AAAGTGCTGGGATTA | 7110 |
rs531677171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69026618 | AGAGTAAAACTCAGT[C/T]TCCAAAACAAACAAA | 7110 |
rs531755962 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69028896 | ATTTTGTGGTGTTAT[A/G]GGCCCCTTTAAAAAA | 7110 |
rs531771602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69046743 | AATGCTTTTGTTCCT[C/T]AGACATTTCTCTTTC | 7110 |
rs531787912 | snp | G/T | 2.24797e-05 | 0.00335252 | intron-variant | TMF1 | GRCh38.p7 | 3:69028015 | AGAGAAATAAAGTTA[G/T]ACAATTTCTGTGATA | 7110 |
rs531866656 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69040546 | GTGGCAAGATGTTAA[C/T]ACCTGATGAATCTAG | 7110 |
rs531924343 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69040952 | ATTTTTCTGGGGCAC[A/G]CGGAAACAATATATA | 7110 |
rs531992817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025842 | CAGAAAATCATTCAC[A/G]TGTTTCCTCTCACTA | 7110 |
rs532202532 | snp | A/G | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050065 | AGGAGTTCAAGACCA[A/G]CCTGGCCAACATGGT | 7110 |
rs532208534 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69033137 | AAATTAGCCAGGCAT[C/G]GTGGCAGACGCCTGT | 7110 |
rs532369307 | snp | C/T | | | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053782 | AAATTAGCTGTACAG[C/T]TACAGTTCCAAGACT | 7110 |
rs532400075 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69039164 | TGTTCTGGCTCACTG[A/C]AACCTCTGCCTCCCA | 7110 |
rs532404495 | snp | G/T | 3.32038e-05 | 0.00407441 | missense | TMF1 | GRCh38.p7 | 3:69033565 | AGCCTATCAGAAAGA[G/T]TCTTCTCTAATTTCT | 7110 |
rs532462420 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69032758 | GGGATTACAGGCATG[C/T]GCCATGACACCCAGC | 7110 |
rs532472275 | snp | C/T | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020212 | CCTGAACATTCTTTT[C/T]ACTTACTTCACTACA | 7110 |
rs532688305 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027152 | AGGCACATGCCACCA[G/T]GCCCGGCTAATTTTT | 7110 |
rs532969043 | snp | A/C | 3.03993e-05 | 0.00389855 | intron-variant | TMF1 | GRCh38.p7 | 3:69027873 | TAAATGGTTACACCA[A/C]AAACAAACAAAAACA | 7110 |
rs532974631 | snp | A/G | 1.66239e-05 | 0.00288299 | missense | TMF1 | GRCh38.p7 | 3:69048064 | GTGAGAGACTGCGTA[A/G]ACGTATTAGATATAC | 7110 |
rs533035613 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048801 | GGAGCACAGACAAAA[A/G]ACTGGGCCTGGCCTG | 7110 |
rs533040625 | in-del | -/TAGACTTGGTTAGATCATCACAGAACCCATTTATTACAACAATGTAA | 0.0240643 | 0.107019 | intron-variant | TMF1 | GRCh38.p7 | 3:69026673 | AATTAAAACTGTAGC[lengthTooLong]TTTGTTGGGTTTTTA | 7110 |
rs533142138 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021944 | CCGCCTTGGCCTCCC[A/G]AAGTGCTGGGATTAC | 7110 |
rs533236330 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020305 | TATATTTGGTACATT[C/T]CACATGCTAAACACT | 7110 |
rs533483538 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029569 | CATGCCTCAGCCTCC[A/G]AGCTGCTGGGATTAC | 7110 |
rs533507459 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69046227 | TTGGAATGTCTAATT[C/G]CTTAGGTCCTACTCA | 7110 |
rs533740703 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053415 | CATGGGAATAGTCAG[C/T]CAGAGTGGTCACCAA | 7110 |
rs533900540 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | TMF1 | GRCh38.p7 | 3:69035904 | GGAAAAAGTGATGGA[G/T]TTATGCATGGTAACT | 7110 |
rs533947727 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020662 | TACTGGAGTTTTTCA[A/C]GAAACTGTTTAAGTT | 7110 |
rs533963860 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021277 | GGTGTCTATACTATC[C/T]ATGGTTTCAGACGTT | 7110 |
rs534069714 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052573 | GTTCACGTGCTAAAA[C/G]CTTGCACCTTGCCAG | 7110 |
rs534088934 | snp | C/T | 1.6591e-05 | 0.00288015 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69033693 | GTTTCGATTCTCTGC[C/T]TCCTGGAGTCTCTGA | 7110 |
rs534094615 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69040554 | ATGTTAACACCTGAT[A/G]AATCTAGGTGATGAA | 7110 |
rs534210536 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027374 | CCTTAAGTGCCTATA[A/G]ACCAAATGATGTGCA | 7110 |
rs534590489 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69042187 | GATTAGAGGCACGCA[C/T]CACCACCACCCGGCT | 7110 |
rs534602417 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029240 | GGTTTCACCATGTTG[C/G]CCAGGCTGGTCTTGA | 7110 |
rs534616445 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69036490 | GAAATAGGTGTATAA[C/G]CGAATGTGTATGTAC | 7110 |
rs534649952 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69035958 | CCCCAATTTTTCTGT[A/G]TTATTATTATTCTAA | 7110 |
rs534785503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037534 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAAGCAG | 7110 |
rs535029238 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69044101 | AGAGAAAATGTCACC[A/G]ATATCTGACATGTAA | 7110 |
rs535048859 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69040345 | AAATATATGCTGGAT[C/T]ACACTTCTGAATTAA | 7110 |
rs535323596 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050153 | CAATCCCAGCTACTC[A/G]GGAGGTTGAGGCACG | 7110 |
rs535427964 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69032308 | ATAGTTGGAACAATA[C/T]AAGTGACTTGTTCCA | 7110 |
rs535526162 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69035900 | ACTTGGAAAAAGTGA[C/T]GGATTTATGCATGGT | 7110 |
rs535535780 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69028457 | TGTTCCAGATCCCAT[C/G]TGAGTTTCACTCAGA | 7110 |
rs535589916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029070 | TGGAGACGGAGTCTC[A/G]CTCTGCTGCCCGGGC | 7110 |
rs535663258 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021983 | GCCACAGCACCTGGC[C/T]GTAAATGAGAGTTTT | 7110 |
rs535671744 | snp | A/G | 1.65663e-05 | 0.002878 | missense | TMF1 | GRCh38.p7 | 3:69047461 | CCTTCATTTATTGGT[A/G]TGGAAGAAACCAAGA | 7110 |
rs535717863 | in-del | -/A | 0.00239568 | 0.0345268 | intron-variant | TMF1 | GRCh38.p7 | 3:69035767 | TGTATAAAACATGTA[-/A]AAAAAAATTTCTAAT | 7110 |
rs535744887 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69040740 | CAGCCTGGCCAACAT[A/G]GTGAAACCCCATCTC | 7110 |
rs535950781 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050979 | AATGAAACTGCAAAG[A/G]GAGACTTGGCTATTC | 7110 |
rs536062982 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69037493 | AAAAAAAAACAAAAA[G/T]TAGCCGGGCATGGTG | 7110 |
rs536125697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69030418 | AGAGGAGAAAGTCTT[C/T]AGGATCTAGAACAAG | 7110 |
rs536183529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69023739 | AACATCCAGATGAGA[C/T]AATTGTGATGATACA | 7110 |
rs536261337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024426 | AAATCCAATTATTTG[C/T]TTGAAAACATTCAAC | 7110 |
rs536421617 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051411 | ACCTGGGAGGCGGAG[A/G]TTGCAGTGAGCCGAG | 7110 |
rs536484219 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69051878 | CCCTCTCTACACCAC[C/T]TAACCTGCCTGCATC | 7110 |
rs536538501 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022539 | TACAGACTTAATTGT[C/G]AAAGCTGGGTGAAAT | 7110 |
rs536608213 | snp | A/G | 1.67984e-05 | 0.00289809 | intron-variant | TMF1 | GRCh38.p7 | 3:69038813 | TGATAATTCATTCTA[A/G]ATGGGTTGCATATTT | 7110 |
rs536668011 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69032351 | GGATGATTCAAAACA[C/G]AATACCCTGAGTCCA | 7110 |
rs536668264 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022355 | AACTTTATTATTTTC[A/G]ATTCATTTTATAGGG | 7110 |
rs536724650 | snp | C/T | 7.17244e-05 | 0.00598808 | intron-variant | TMF1 | GRCh38.p7 | 3:69043747 | ACTTTAAATTTCAAT[C/T]ACCTTTTTAGCAGCA | 7110 |
rs536728831 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69033080 | GATTTAGCAATGGAC[A/G]AGAAAAAAAAATCGA | 7110 |
rs536734697 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025425 | CATTGATATATGTGA[C/T]ACATTTTGGGCTTCA | 7110 |
rs536751469 | snp | G/T | 8.29208e-05 | 0.00643844 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69038570 | ATTGCTTACTTGAAT[G/T]GCTAATGTTTCTTGC | 7110 |
rs536771240 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69026104 | CTTGCGTTCCTTAGG[A/G]AGTAAAAAAAATTCT | 7110 |
rs536805248 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69042488 | ATAAATCCCAGAGTT[A/T]CACACTTTGAATGTC | 7110 |
rs536864552 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69043339 | CATGGCCAGCTAATC[A/T]TTGTATTTTTTGTAG | 7110 |
rs536864877 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69036266 | GTAAAAAGGATGTAG[G/T]AGATAGAAATAGGTG | 7110 |
rs536928636 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69037010 | GAGAGGCACAAAATA[C/T]TGACAAATCCTATAT | 7110 |
rs536987957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69029733 | GGCGTGAGCCACGGC[A/G]CCCGGCCCAACAACA | 7110 |
rs537107189 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69023576 | ATTCTCCCCATATAT[G/T]ACTTCTCTCCCATTA | 7110 |
rs537180585 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024669 | TTTGCCAATTCAAGT[C/T]CTTTAATATTTTCAT | 7110 |
rs537279714 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050911 | ATGCTGAACTGTTCC[C/T]TAGACTTAAGAGTCA | 7110 |
rs537399445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037629 | CCTGGGCAACAAGAG[C/T]GAAACTCTGTCTCAC | 7110 |
rs537462150 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69038157 | CATATGCCCATCAAC[C/T]GATGATTTGATAAGA | 7110 |
rs537594182 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69032213 | GACAGCAGCCCCAAA[C/G]GTATCTAAGAGTCCA | 7110 |
rs537880392 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052525 | CCCGGAAGGAATATT[C/T]AAGTTTTCGTGTGTG | 7110 |
rs537965071 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053660 | ACAGTAAAAACTTGC[A/G]TGTTAAAACTAACAA | 7110 |
rs538006705 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69039365 | TCGCAGCCTCCGAAA[C/G]TGTTGGGATTACAGG | 7110 |
rs538063190 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025174 | GGTAAATCTGAATAG[A/G]ACAGGCATTCACAGC | 7110 |
rs538068240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039898 | GGAACTGGATATTGA[C/T]ACGGTCTTAAAGAAT | 7110 |
rs538149733 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69026351 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCAAGG | 7110 |
rs538264195 | snp | C/T | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050668 | ATGAAAAAACAGAGT[C/T]ACTCCAGCAAGGTTA | 7110 |
rs538277506 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69051432 | GTGAGCCGAGATCGC[G/T]CCACTGCACTCCAGC | 7110 |
rs538506252 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024467 | TCTAATCTAAGGAAA[G/T]GACATATATTTCAGT | 7110 |
rs538560423 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69026931 | TATCGGTAGTTTAAA[C/T]ATATTATGCTAACTC | 7110 |
rs538718190 | snp | A/C | 0.0189856 | 0.0955633 | intron-variant | TMF1 | GRCh38.p7 | 3:69026709 | AGAACCCATTTATTA[A/C]AACAATGTAATTTGT | 7110 |
rs538828904 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69031465 | ACCAATAAAACTTTG[C/G]AAATCTGAATAAAAT | 7110 |
rs538860753 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | TMF1 | GRCh38.p7 | 3:69045972 | TAGGTGGGAGGACTG[C/G]TTGAGCCCAGGAGGT | 7110 |
rs538875767 | snp | C/T | 6.6379e-05 | 0.00576065 | missense | TMF1 | GRCh38.p7 | 3:69038901 | CTTCAAGTTCATCCA[C/T]GTCTACCTGAAGACG | 7110 |
rs539199546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69035341 | GTTAAGGCAAAGAAA[C/T]GCAAACAAATATGTA | 7110 |
rs539260708 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69045449 | GCCTGGGTGACAAGA[A/G]TGAAACTCCATCTCA | 7110 |
rs539296215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039333 | TCTCAAACTCCTGGC[C/T]TCAAGTGATCTGCCT | 7110 |
rs539345511 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054284 | ACTTTGGGAAGCCGA[G/T]GGGGGCGGGGGGGGG | 7110 |
rs539359433 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69033146 | AGGCATGGTGGCAGA[C/T]GCCTGTAATCCCAGC | 7110 |
rs539395331 | snp | C/T | 3.32939e-05 | 0.00407993 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69047418 | AGCAGGTTCACACTG[C/T]TCAGCCACCTTGTCT | 7110 |
rs539553941 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027405 | CTGGTTTCAGTGACA[G/T]ACAATTAAATTCATT | 7110 |
rs539648347 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053540 | CATATTTGAATATTT[C/T]ACCCCACTGCAAGGA | 7110 |
rs539849617 | snp | A/T | 3.45328e-05 | 0.00415514 | missense, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048555 | TCCACTGACAGGGGA[A/T]CTTATTCCTTTAACA | 7110 |
rs539856126 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69032738 | CCTCAGCCTCCCAAA[C/T]AGCTGGGATTACAGG | 7110 |
rs539976198 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69026465 | GCTGGGCGTGGTGGC[A/G]CATGCCTGTAATCCC | 7110 |
rs540081619 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69045064 | GGAAATTTAAAGCCT[C/T]TATATTTTAGCTAGG | 7110 |
rs540198016 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053821 | TACAGCTTTGGTGAA[A/G]TGACCTACCTAAACC | 7110 |
rs540219751 | snp | A/G | | | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019560 | GGGAGGCTAAGGCAG[A/G]AGGATCACTTGAACC | 7110 |
rs540305248 | snp | A/G | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022431 | CATTGCAAAATCATT[A/G]TAAATAAATTTTCTC | 7110 |
rs540392401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051664 | GTCGAGGGAGAGCTT[A/G]AGGGCAAGACCAACC | 7110 |
rs540512044 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69045642 | AAAATTAGCCAGGCA[C/T]GGTAGCATACGTCTG | 7110 |
rs540811927 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69029158 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGAATTA | 7110 |
rs540821439 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69040802 | TGGCAGGTAGCTATA[A/G]TCTCAGCTATTCGGG | 7110 |
rs540864385 | snp | A/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026298 | AAATGGCTTCTTAAG[A/T]CAAAAATACAATATT | 7110 |
rs541019601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69036506 | CGAATGTGTATGTAC[A/G]CAGAACATGTAAGTA | 7110 |
rs541021354 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69029044 | TATTACTTTATTTAT[A/T]TTTTTTTTTTTGGAG | 7110 |
rs541042669 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029535 | CTGCAACTTCCGCCT[C/T]CCGGGTGTAAGCGAT | 7110 |
rs541130437 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69026533 | GGGAGGTGAGGTTGC[A/G]GTGAGCCGAGATAGC | 7110 |
rs541330602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027660 | CACACATAAAATATA[C/T]TAACAATAGCTGATG | 7110 |
rs541399424 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69053011 | TCTAAGCCAGAATAG[C/T]AGCCCTCACCAGACA | 7110 |
rs541429562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037179 | GCAAATGAAAAGACA[C/T]CCAACATCATTAGTC | 7110 |
rs541632931 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69047072 | ACTAATAAGCATAAC[A/G]GAATTTTGAAGTGAT | 7110 |
rs541830145 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69041906 | GAAATAAAAAGAGAG[A/T]TTCACTTGACCACGT | 7110 |
rs542078338 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69025805 | GTTCTGTCAATTTTT[A/G]CTTTAAATGTCTTCT | 7110 |
rs542081071 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69033465 | CTATCAGATCAAATG[A/G]ATTTCAATTTCATAC | 7110 |
rs542169848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | TMF1, MIR3136 | GRCh38.p7 | 3:69048668 | AGAAAAAATACCCTA[C/T]GAAATACCTGTAATT | 7110 |
rs542358942 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69040405 | ACCTGTCAAGGAAAA[C/T]GTACTTGCCCTTGGG | 7110 |
rs542989645 | snp | A/C/T | 1.67942e-05 | 0.00289772 | intron-variant | TMF1 | GRCh38.p7 | 3:69033742 | CATTACCAATGACAG[A/C/T]AATAAAAACATTAAA | 7110 |
rs543004845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69031658 | GAAAAAAAGAGCAAT[A/G]GGTAAGATTCTGAGA | 7110 |
rs543006795 | snp | C/T | 3.33056e-05 | 0.00408065 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69024091 | GGGTATCTCCTTCAC[C/T]TTCTCTTCAAGTTCA | 7110 |
rs543043972 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024736 | CTACTTCTGAGTGTA[C/T]TGTGTTTAACACTGA | 7110 |
rs543161552 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049408 | AAAGCCTCAAACCAA[G/T]ATAATGGTGACAAAT | 7110 |
rs543178800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69044259 | CTAATACTAAAAGAC[C/T]AAAAACGAAAGGAAA | 7110 |
rs543258104 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69028712 | GTAAAATTTCCAAGG[A/G]AGAACAGAGGGTTAA | 7110 |
rs543343163 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69031027 | GTGAATGGTTAAATA[A/T]ACGTGGTACATACTA | 7110 |
rs543409353 | snp | C/T | 0.000166052 | 0.00911035 | missense | TMF1 | GRCh38.p7 | 3:69029965 | TCTTCTGTAGCTGCA[C/T]GTTCTCTCTCAACTG | 7110 |
rs543507300 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69025778 | TTCCATTACCAGGTT[C/T]GAACAAAAATGGTTC | 7110 |
rs543733396 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021467 | CTACTAAAATGAAGA[A/C]AATTAATTTTATGAA | 7110 |
rs543818900 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69030925 | AAATGAAAACTTAGG[G/T]TCACACTAAAACCTG | 7110 |
rs543849458 | snp | C/G | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049075 | TATAGTTATGAGCTA[C/G]ACAAAGGGCAACACT | 7110 |
rs543866770 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029363 | TAATAACCCTAACTT[C/T]AAATGCTAAAAGTGA | 7110 |
rs543900149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69031810 | GTATGTTTGTCCTGT[A/G]GCTTTGCCTATATGC | 7110 |
rs543967445 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050194 | GAGCTCAGGAGACAG[A/C]ATCTGCAGTGAACAG | 7110 |
rs544000993 | snp | C/T | 0.000153484 | 0.00875889 | intron-variant | TMF1 | GRCh38.p7 | 3:69042964 | GACTTTCACTCTAAG[C/T]ACAGTTCTCATTTCT | 7110 |
rs544064516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69043605 | AGCCACCACACGTGG[C/T]CAAAAATCTACAATT | 7110 |
rs544122797 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69037270 | GAGGCCAAGGCAGGC[A/G]GATCACGAGGTCAGG | 7110 |
rs544127952 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | TMF1 | GRCh38.p7 | 3:69051234 | GTAATCCCAGCACTT[C/T]AGGAGGCCGAGGTGG | 7110 |
rs544190009 | snp | A/T | 0.00021231 | 0.010301 | intron-variant | TMF1 | GRCh38.p7 | 3:69044466 | CAGAAAATGTGTAAC[A/T]TTATTCACATTTGCA | 7110 |
rs544358394 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69032672 | CTGGAGTGCTGTAGC[A/G]CAATCTCAGCTCACT | 7110 |
rs544445353 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69024995 | CTGTAAAACATTTCA[A/G]TATTTCTGACTGCAT | 7110 |
rs544543511 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69039382 | GTTGGGATTACAGGC[A/G]TGAGCCACCCCACTC | 7110 |
rs544571844 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69051167 | AAGCTCTCTCTGGGA[G/T]TTGTTCTGAAGATGA | 7110 |
rs544643988 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052915 | TTTAGGAGATGATTA[A/G]ATGATGATGGAGCCC | 7110 |
rs544698111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69044936 | CATAAATGCACTAGG[C/T]GACATGTATAAGAAT | 7110 |
rs544705418 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69046343 | TGAACTTAGAAATCA[C/G]TTACCTTCTTAAATA | 7110 |
rs544745437 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69045095 | TGGTGGATACACAAG[G/T]GTCTATTTTCTGTAT | 7110 |
rs544768020 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037730 | AGAATTGCTTGAATC[C/T]GGGAGGCAGAGGTTG | 7110 |
rs545227036 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69031090 | TACCGATACAAAAAC[A/C]ACTGTGTGAACCTCT | 7110 |
rs545432651 | in-del | -/A | 0.000541553 | 0.0164464 | intron-variant | TMF1 | GRCh38.p7 | 3:69028017 | GAAATAAAGTTAGAC[-/A]AATTTCTGTGATAGT | 7110 |
rs545538391 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69038386 | CAATACTGGTATCAC[A/G]TAAGCATTACTTTAA | 7110 |
rs545575825 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027026 | TTTGAGAAAGAGTCT[C/T]GATCTGTTGCCCAGG | 7110 |
rs545703520 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69026667 | TTTACTAATTAAAAC[G/T]GTAGCTAGACTTGGT | 7110 |
rs545738735 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69033428 | AAAATGTAAAAATCT[A/T]CATATTAGACACAAA | 7110 |
rs545762421 | snp | A/G | 4.97006e-05 | 0.00498476 | missense | TMF1 | GRCh38.p7 | 3:69047629 | GTTGAAGAATTAACT[A/G]TAATAGGCACTAAAG | 7110 |
rs545790097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69026570 | GGTGGCGGTGAGCTG[A/G]GATAGCACCACTACA | 7110 |
rs545825998 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69040850 | TTGCTTGAACCTGGG[A/C]GGCGGAGGTTGCAGT | 7110 |
rs545987181 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69045742 | ACAGGGCAAGACTCC[A/G]CCTCAAAAAATAAAT | 7110 |
rs546011219 | snp | A/G | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050168 | GGGAGGTTGAGGCAC[A/G]AGAATCACTTGAGCT | 7110 |
rs546050353 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | TMF1 | GRCh38.p7 | 3:69039196 | CTTCAGGCAATTTTC[A/G]TGCCTTAGCCTCCCA | 7110 |
rs546106346 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034153 | TCCTTCCAAGAGAGT[G/T]AGATTGTGTAATACA | 7110 |
rs546113276 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039449 | AATCCTTCTTACATG[A/G]TATACCCCATTAAAT | 7110 |
rs546119616 | in-del | -/ACTT | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022815 | AATATATATATAAAC[-/ACTT]ACAAATTATAGATAC | 7110 |
rs546199364 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69025132 | TTACCCCTCCTTCCC[A/G]GGGTAGCTGGAACAA | 7110 |
rs546273135 | snp | A/G | 6.62449e-05 | 0.00575483 | missense | TMF1 | GRCh38.p7 | 3:69035049 | CACCGATCTCATGGC[A/G]TAAATAATCCTCCTT | 7110 |
rs546305648 | in-del | -/CT | 0.00557542 | 0.0525036 | upstream-variant-2KB | TMF1 | GRCh38.p7 | 3:69052770 | TGCATAAAGCACAAC[-/CT]CTCTCTCAAAATAGT | 7110 |
rs546442311 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037498 | AAAACAAAAATTAGC[C/T]GGGCATGGTGGTGGG | 7110 |
rs546553729 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69046501 | TATTTAACCTGATTA[A/G]CAGAATCTGGCACTT | 7110 |
rs546704179 | snp | C/T | 1.65699e-05 | 0.00287831 | missense | TMF1 | GRCh38.p7 | 3:69039610 | TGTTCAGCTTTGCAA[C/T]CATATTTTCATTCTC | 7110 |
rs546736889 | snp | G/T | 1.66974e-05 | 0.00288936 | missense | TMF1 | GRCh38.p7 | 3:69044588 | TTTTCATTCAGAAAT[G/T]CAACTGTCTGGATAA | 7110 |
rs546769213 | snp | A/G | 0.00028575 | 0.0119496 | intron-variant | TMF1 | GRCh38.p7 | 3:69033542 | CATAAAAACTAAAGC[A/G]GTTACCAAGCCTATC | 7110 |
rs546771835 | snp | C/T | 1.66286e-05 | 0.0028834 | missense | TMF1 | GRCh38.p7 | 3:69051966 | CTCCATACGGAATGG[C/T]CTCGGCCCAGATGCT | 7110 |
rs546838022 | snp | G/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69045977 | GGGAGGACTGCTTGA[G/T]CCCAGGAGGTCAAGG | 7110 |
rs546874824 | snp | C/T | | | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049690 | GCGCTACAAAGAAAA[C/T]GACTGTTTTCTTGGG | 7110 |
rs547045073 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69033094 | CAAGAAAAAAAAATC[A/G]AGTGCAGCAGTCTAC | 7110 |
rs547099678 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69026173 | AGAACATTTCCTAGG[A/G]TTAATGAGAACAAAG | 7110 |
rs547396246 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, upstream-variant-2KB | UBA3, TMF1 | GRCh38.p7 | 3:69054257 | ATGGTGGCTCATGCC[C/T]GTAATCCCAGCACTT | 7110 |
rs547451948 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69023639 | TTTGTTCCATGGTGG[C/T]ATAAGTATTACCCGG | 7110 |
rs547475197 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69040555 | TGTTAACACCTGATG[A/C]ATCTAGGTGATGAAG | 7110 |
rs547520706 | snp | C/T | 0.000399281 | 0.0141238 | missense | TMF1 | GRCh38.p7 | 3:69047965 | CCTGATGAAAAGGTA[C/T]TAACAGGAGGAGAAG | 7110 |
rs547622964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69027121 | CCACCTCTGCCTCCC[A/G]AGTAGCTGGGATTAC | 7110 |
rs547642584 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69041313 | GTGTTCCTATATTTC[C/T]CTCTCACTGAACTAA | 7110 |
rs547761477 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69037410 | TTTGGGAGGCGGAGG[C/T]GGGTGGATCACCAGA | 7110 |
rs547892764 | snp | A/C | | | intron-variant | TMF1 | GRCh38.p7 | 3:69031113 | GAACCTCTTCCTGGG[A/C]ATTACACTGAGTGAA | 7110 |
rs548061313 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69035717 | AGTTGCAAATGTCGA[C/T]ACAACATGAATATAA | 7110 |
rs548063706 | snp | C/G | | | missense | TMF1 | GRCh38.p7 | 3:69023314 | TGTTGTACCTTTGAT[C/G]CAAATCCTGAAAAAT | 7110 |
rs548368102 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69020496 | AAAATGTTATTTGCA[C/G]CTTTTTTCTTTCAAG | 7110 |
rs548602737 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | TMF1 | GRCh38.p7 | 3:69019387 | AACTTAGGGCCGGGC[A/G]CAGTGGCTTATGCCT | 7110 |
rs548628598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69037405 | AGCACTTTGGGAGGC[A/G]GAGGCGGGTGGATCA | 7110 |
rs548668097 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69042171 | CCTCCTGAGTAGCTG[A/G]GATTAGAGGCACGCA | 7110 |
rs548707306 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021125 | AAAGAGACAGACATA[C/T]CACATTTACATCACT | 7110 |
rs548727443 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039923 | AAGAATCACTCTCAT[A/C]TATCACCTACTAATT | 7110 |
rs548954468 | snp | C/T | | | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69022354 | GAACTTTATTATTTT[C/T]GATTCATTTTATAGG | 7110 |
rs549003789 | in-del | -/ATT | 0.00199481 | 0.0315187 | intron-variant | TMF1 | GRCh38.p7 | 3:69044882 | TCTTTGATATAGAAA[-/ATT]TCACTTTTAGGTATA | 7110 |
rs549176751 | in-del | -/T | 0.463881 | 0.12944 | intron-variant | TMF1 | GRCh38.p7 | 3:69029042 | CTATTACTTTATTTA[-/T]TTTTTTTTTTTTTGG | 7110 |
rs549198603 | snp | C/T | 0.000447031 | 0.0149437 | synonymous-codon | TMF1 | GRCh38.p7 | 3:69048447 | ATCGACCACAGTCCT[C/T]CGAACTGGCTTTGTG | 7110 |
rs549210657 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69044078 | ACCTCAAAGAAAATC[C/T]GTTAGAAAGAGAAAA | 7110 |
rs549437356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050684 | ACTCCAGCAAGGTTA[C/T]ATGACATCTTGTAAA | 7110 |
rs549461412 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69029725 | GGATTACAGGCGTGA[A/G]CCACGGCGCCCGGCC | 7110 |
rs549511812 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | TMF1 | GRCh38.p7 | 3:69031372 | GGAACTGTTCAATAT[C/G]TTGACTATGGTAATG | 7110 |
rs549613867 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69027119 | TCCCACCTCTGCCTC[C/T]CGAGTAGCTGGGATT | 7110 |
rs549626941 | in-del | -/A | | | intron-variant | TMF1 | GRCh38.p7 | 3:69043135 | GCAAGTGTTAATATG[-/A]AAAATATAAATGAGA | 7110 |
rs549657401 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69034388 | TGAGGCAGGAGAATC[A/G]CTTGAACCCAGGAGG | 7110 |
rs550025834 | in-del | -/TGAAAA | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69043084 | CTAAGAAAACAACTT[-/TGAAAA]TGATATTCAAAACCT | 7110 |
rs550030365 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049918 | AGAGAGCACAAGTAA[C/G]TAAAAGCTTCTAAAA | 7110 |
rs550133519 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69037768 | CTGAGATCGTGCCAC[C/T]GTGCTCCAGTCTGGC | 7110 |
rs550141046 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | TMF1 | GRCh38.p7 | 3:69029046 | TTACTTTATTTATTT[A/T]TTTTTTTTTGGAGAC | 7110 |
rs550149937 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69050877 | CCCAACACCAGCAAA[C/T]CTTTACCCCACACAT | 7110 |
rs550186226 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | TMF1 | GRCh38.p7 | 3:69021293 | ATGGTTTCAGACGTT[C/T]ACTGGGGGTCTTGGA | 7110 |
rs550215272 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69047000 | TTTGGCACATCTATC[C/T]GCAAAGGAGGTGAAG | 7110 |
rs550348119 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69043363 | TTTGTAGAGATGAGG[A/T]CTCGCCATGTTGCCC | 7110 |
rs550368743 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69035767 | ATGTATAAAACATGT[A/T]AAAAAAATTTCTAAT | 7110 |
rs550411151 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69043959 | ATTCTCAAAAGGAAG[A/G]TAACTTTTCTCTGAC | 7110 |
rs550445441 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | TMF1 | GRCh38.p7 | 3:69029589 | GCTGGGATTACAGGC[A/G]CACACCATCACACCT | 7110 |
rs550471368 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TMF1 | GRCh38.p7 | 3:69037413 | GGGAGGCGGAGGCGG[A/G]TGGATCACCAGAGGT | 7110 |
rs550491242 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | TMF1 | GRCh38.p7 | 3:69024256 | AATATAAAAATATTT[A/C]ATGTGTGTGTGGTTT | 7110 |
rs550627704 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69024337 | TTTCTTAAGTAAAGG[A/G]AACAGTGGCAGAAAA | 7110 |
rs550746331 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | TMF1 | GRCh38.p7 | 3:69045849 | AAGACCGCTTGAGCC[A/C]AGGAGTTCAAGACCA | 7110 |
rs550899548 | snp | A/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69045781 | TAAAATAAAAGTAGG[A/G]CTGGACACGGGTTCA | 7110 |
rs550937991 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69045215 | GTAATCCCAGCACTT[C/T]GGGAGGCTGAGGTGG | 7110 |
rs551057316 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69036939 | GCTAGACTTTGTTAA[A/C]ATTAAAACCTTTTGG | 7110 |
rs551107132 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69032234 | TAAGAGTCCACTGAA[A/T]ACTATTTGAAAGTCA | 7110 |
rs551107281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69039246 | GTGCACCACCACGCC[C/T]GGCTAATTTTTGTAT | 7110 |
rs551120610 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69029720 | TGCTGGGATTACAGG[C/T]GTGAGCCACGGCGCC | 7110 |
rs551145494 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | TMF1, MIR3136 | GRCh38.p7 | 3:69049143 | ATAATCCCAACACTA[A/G]AAGAGTCATTTGAGT | 7110 |
rs551266737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69043326 | ACGCATGTACCACCA[C/T]GGCCAGCTAATCTTT | 7110 |
rs551280376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051846 | ACTTCCTGAAAACTC[C/T]CTCAGCAAGGAAGGA | 7110 |
rs551305621 | in-del | -/G | | | intron-variant | TMF1 | GRCh38.p7 | 3:69037934 | GGATGTGGAGAAACT[-/G]AAACCCTCACCTATT | 7110 |
rs551337870 | snp | C/T | | | intron-variant | TMF1 | GRCh38.p7 | 3:69040951 | AATTTTTCTGGGGCA[C/T]GCGGAAACAATATAT | 7110 |
rs551448356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69030131 | ACTGATAACTATTTA[C/T]TGCCTAAGGCAGGAC | 7110 |
rs551531251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | TMF1 | GRCh38.p7 | 3:69051723 | AAGCCTCGCACCCAG[A/G]ACCAAAGAAAGACAA | 7110 |
rs551540062 | in-del | -/ATT | 0.00119737 | 0.0244387 | intron-variant | TMF1 | GRCh38.p7 | 3:69041089 | TCATTCTCTGACAAA[-/ATT]ATTAAATTACAAAAT | 7110 |