SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs11368 | snp | A/G | 0.499075 | 0.0214901 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59954051 | TGTAATTACCTGACA[A/G]ATGAGAAGAATTGGC | 51136 |
rs180511 | snp | C/T | 0.189576 | 0.242588 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955087 | CTTTACCCTCATGAC[C/T]GTGACTGACTTGGGT | 51136 |
rs180512 | snp | G/T | 0.190205 | 0.242744 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954470 | GGGTCAAATAATACA[G/T]GGCTATAGATTTTAT | 51136 |
rs180514 | snp | C/T | 0.158632 | 0.232706 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953288 | atcacttgaaccagt[C/T]gggggcggaggttgc | 51136 |
rs767811 | snp | G/T | 0 | 0 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962691 | ATGTTTATTTTTAAT[G/T]TGTGTCATTGTTAGC | 51136 |
rs975547 | snp | A/C | 0.190205 | 0.242744 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963881 | CGGGGAGGTAATATT[A/C]TTGGTGGCACCATTA | 51136 |
rs1024637 | snp | A/G | 0.479502 | 0.0991411 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961532 | AAGTTACACGAGCCC[A/G]TCATATAAATCATTG | 51136 |
rs1860294 | snp | G/T | 0.190205 | 0.242744 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959484 | TTGTTATTATTGGTC[G/T]TTGTTTCTGAAAGTA | 51136 |
rs2159286 | snp | A/G | 0.190519 | 0.242821 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956878 | TCTCTCCATGCCTGC[A/G]CCCCTCAACCTAATA | 51136 |
rs4968401 | snp | C/T | 0.487558 | 0.0778863 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963369 | GTATCCTTTATTCAC[C/T]AAAGGAGTAGCAAAT | 51136 |
rs7219051 | snp | A/G | 0.241053 | 0.24984 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955349 | ACAAGCTTTTAAGAC[A/G]TTACTCATCTGGCAT | 51136 |
rs7219089 | snp | C/T | 0.323671 | 0.238899 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955504 | TTCTTGAGAGTATTT[C/T]GGCACAAATCTTACA | 51136 |
rs7221472 | snp | C/T | 0.324382 | 0.238678 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959376 | caactccagtgaaac[C/T]aGGTCTTCTAATATT | 51136 |
rs8075105 | snp | A/T | 0.190205 | 0.242744 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960329 | GTTACTGTTTTATAC[A/T]ACTTTAGTGACCAAA | 51136 |
rs8081368 | snp | C/G | 0.240765 | 0.249829 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965245 | GAAAAACCTGTCTTG[C/G]GTGGGGTATAGAGGA | 51136 |
rs9709385 | snp | G/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965845 | aaaatacaaaaatta[G/T]ccgggtgtggtggtg | 51136 |
rs9709408 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965859 | agccgggtgtggtgg[C/T]gcgtgcctgtaatct | 51136 |
rs9709409 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965863 | gggtgtggtggtgcg[C/T]gcctgtaatctcagc | 51136 |
rs9912341 | snp | A/G | 0.139564 | 0.224285 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965927 | acccgggaggcggag[A/G]ttgcagtgagccggg | 51136 |
rs11079391 | snp | C/T | 0.0952156 | 0.196321 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960424 | TATGTTTCAAAGAAG[C/T]CAAGTCTTCTCTCaa | 51136 |
rs11406596 | in-del | -/A/AA | 0.5 | 0 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960437 | GCCAAGTCTTCTCTC[-/A/AA]AAAAAAAAAAAAAAA | 51136 |
rs11554818 | snp | C/T | 0 | 0 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952652 | TCAGGAAAGAATACC[C/T]GAGTTCTCTAAAACC | 51136 |
rs11868009 | snp | A/C | 0.487113 | 0.0792303 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959138 | tttcttatcaattct[A/C]cttagcctctcaaac | 51136 |
rs12051810 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955863 | TAGGAACCTTTCAGG[C/G]TACTAAGTGGTAAAT | 51136 |
rs12600680 | snp | C/T | 0.324619 | 0.238604 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960013 | TAAGATACAAAGTGC[C/T]ATGAAATATATGATT | 51136 |
rs16943969 | snp | A/G | 0.24134 | 0.24985 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953792 | ATCCAATTATAAAAT[A/G]GCCTGTTTTTTAATC | 51136 |
rs17850123 | snp | A/G | 0 | 0 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963188 | ATCCTCACTGCTTCC[A/G]GTTCCTGGAGGACTG | 51136 |
rs28733789 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961322 | AGATTACAGGCATGA[A/G]CCACTGTGCCTTGCC | 51136 |
rs34068842 | in-del | -/T | 0.494315 | 0.0530107 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953191 | GAATGAAAGGGATTC[-/T]TTTTTTTTTTTTTTT | 51136 |
rs34229958 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959143 | TATCAATTCTCCTTA[-/G]CCTCTCAAACTTAAC | 51136 |
rs34511510 | in-del | -/T | 0 | 0 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59961903 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTCGT | 51136 |
rs34533381 | in-del | -/A | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956682 | ATATGTCACATCTAA[-/A]TCATTTTGTGCTGAG | 51136 |
rs34816517 | in-del | -/C | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952217 | TTTTCTATACTATTC[-/C]AAATCATCAAGTAAG | 51136 |
rs35264935 | in-del | -/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957769 | GAACTGCCTGAACCC[-/C]AGGAGGCGGAGGTTG | 51136 |
rs35344838 | in-del | -/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956147 | ACAAACAAAGCCCCC[-/C]ATTTGTGGATTAAAA | 51136 |
rs35957078 | in-del | -/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955075 | GATGTAAGAACACCC[-/C]AAGTCAGTCACGGTC | 51136 |
rs58997167 | snp | A/C | 0.0387552 | 0.1337 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957861 | AAACAAAACAAAACC[A/C]AAAAAAAAGATACAA | 51136 |
rs59767604 | snp | C/G | 0.240765 | 0.249829 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963978 | AGGTAACTCTTTAGT[C/G]TGAATAAGCAGTTAC | 51136 |
rs61751975 | snp | A/G | 0.0121533 | 0.0769997 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963203 | AGTTCCTGGAGGACT[A/G]TGCAGTTGGCTACGA | 51136 |
rs61752305 | snp | A/G/T | 0.000576407 | 0.016967 | synonymous-codon, missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962995 | TGTGGGAGTGACCCC[A/G/T]TAAGCGACTGTGTAC | 51136 |
rs62081840 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963509 | CAAAAAAAAAAAAGT[A/T]GAGCTGCAAATGCTT | 51136 |
rs71370154 | in-del | -/T | 0.5 | 0 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59961882 | TGCCTGGCCCAGGTC[-/T]TTTTTTTTTTTTTTT | 51136 |
rs73318983 | snp | A/C | 0.000267206 | 0.0115556 | missense | RNFT1 | GRCh38.p7 | 17:59954106 | GAACAAATATCATCC[A/C]CATCTGAACACTGTC | 51136 |
rs74346234 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955428 | AGACTTGAACAAATC[A/C]AAGTATTGATGACTG | 51136 |
rs74348089 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953855 | TTTTCCCCTTCATAC[G/T]CTCCTCTGCATAAAA | 51136 |
rs74555505 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963807 | CTGCACTTAGGTGAC[C/T]TACAAATTAGATTTT | 51136 |
rs75137032 | snp | G/T | 0 | 0 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953207 | TTTTTTTTTTTTTTT[G/T]AGATGGAGACTGAAG | 51136 |
rs75400693 | snp | A/C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966287 | AGGAGACCCCCACCT[A/C/T]AAAAAAAAACACATT | 51136 |
rs75421338 | snp | C/T | 0.0232847 | 0.105357 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964722 | CCGCAAGCTCTTCTC[C/T]CAGCCCGGCGGCAAC | 51136 |
rs75460876 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963718 | AGTATTTTTTAATGG[C/T]TGGAAATGTTAGGAA | 51136 |
rs76147107 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963507 | ACCAAAAAAAAAAAA[G/T]TTGAGCTGCAAATGC | 51136 |
rs76419616 | snp | C/T | 0.356383 | 0.226236 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964765 | CGCGCTCCCCGGACG[C/T]TCTCACGCGCGCGCG | 51136 |
rs76525517 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966288 | GGAGACCCCCACCTC[A/C]AAAAAAAACACATTG | 51136 |
rs77495043 | snp | A/C | 1.67719e-05 | 0.0028958 | missense | RNFT1 | GRCh38.p7 | 17:59956514 | AAAATATTCGTAAAA[A/C]CTGTCTGAAAGTTCT | 51136 |
rs77530104 | snp | A/C | | | splice-acceptor-variant | RNFT1 | GRCh38.p7 | 17:59957383 | CATATACCAGTAACC[A/C]TAAAAAATAAGAAGA | 51136 |
rs78095669 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963506 | CACCAAAAAAAAAAA[A/G]GTTGAGCTGCAAATG | 51136 |
rs78261818 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956067 | GACATGATTTTTGGC[A/G]GTGAGCTTTCTAAAC | 51136 |
rs78349854 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955425 | AGGAGACTTGAACAA[A/G]TCCAAGTATTGATGA | 51136 |
rs78559369 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963495 | GGGAACATTTGCACC[A/C]AAAAAAAAAAAGTTG | 51136 |
rs79006987 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953247 | GTCACCCAGGCCGGA[A/G]TGCAATGGCACCATC | 51136 |
rs79015397 | snp | A/G | 0.5 | 0 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959929 | AGAAAAAAAAAAAAA[A/G]AGCTCTCGCTTATGA | 51136 |
rs111339435 | snp | A/C | 0.029116 | 0.117091 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961498 | AAGGTGAAATTTTAG[A/C]AACTCATCCTCTTTT | 51136 |
rs111857062 | snp | C/T | 0.069869 | 0.173358 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960052 | AATGTAATTGTGTAT[C/T]TGGACCTCTAATTAC | 51136 |
rs111918363 | snp | A/G | 0.239037 | 0.24976 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953393 | TTTAGTAGAGACAGG[A/G]TTTCACCATGTTGGT | 51136 |
rs111953367 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963383 | CTAAAGGAGTAGCAA[A/G]TAATCACAACAGATG | 51136 |
rs112263224 | snp | C/T | 0.5 | 0 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953949 | CCACTAAACACTAGA[C/T]TTTTTTTTTTTTGCC | 51136 |
rs112345334 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959342 | CCTCCAAACTATATC[C/T]CAGATTTGCCCATCT | 51136 |
rs112481698 | snp | A/G | 0.000547995 | 0.0165438 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958731 | AACTCATCAATACCA[A/G]ACATCTGCTGTGTTT | 51136 |
rs112664639 | snp | A/C | 0.5 | 0 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957855 | ATCTCAAAACAAAAC[A/C]AAACCAAAAAAAAAG | 51136 |
rs112808730 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956139 | TTAATAGGAACAAAC[A/G]AAGCCCCCATTTGTG | 51136 |
rs112835092 | snp | A/G/T | 0.000216245 | 0.0103963 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962562 | AAAACCTGATTTACA[A/G/T]TGCTTTTGTTTGCAT | 51136 |
rs113104342 | snp | C/G | 0.0562307 | 0.157967 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957809 | AAGATCACACCACTG[C/G]ACTCCAGCCTGGGCA | 51136 |
rs113341992 | snp | A/G | 0.5 | 0 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958167 | CTAAGCTGAAATAAT[A/G]CAGATAATTAAGCTA | 51136 |
rs113569159 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958589 | TTCACAATAATGGAA[G/T]GGAGGATCATTTTGC | 51136 |
rs113699640 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957917 | GTAAAACCTATGTGA[A/G]TATGTTTTTGCTGAT | 51136 |
rs114788792 | snp | A/G | 0.0865458 | 0.189163 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955881 | CTAAGTGGTAAATTA[A/G]GGTTCTCTATGACAT | 51136 |
rs115039364 | snp | G/T | 0.000263535 | 0.011476 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963008 | CCGTAAGCGACTGTG[G/T]ACACATCCATGGGCA | 51136 |
rs115215316 | snp | A/T | 0.00914312 | 0.0669923 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952634 | TTTATTCTGAAAACA[A/T]TGTCAGGAAAGAATA | 51136 |
rs115465451 | snp | A/C/T | 0.00279162 | 0.0372561 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956927 | CTAGTTTAAGAATTA[A/C/T]GTGTATGACAATGTT | 51136 |
rs117634246 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955702 | CTGGCCAGTTAGTCT[C/T]GTTTACTTTGTAGAC | 51136 |
rs138113380 | snp | C/T | 8.4679e-05 | 0.00650633 | splice-acceptor-variant | RNFT1 | GRCh38.p7 | 17:59958446 | TTAAAAAAATTAAGC[C/T]ACCAAAAGAAAAACA | 51136 |
rs138189792 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958878 | TCCCTGAATAATTTT[C/T]TTTCTAGACTTTTAA | 51136 |
rs138794420 | snp | C/T | 0.0120912 | 0.0768076 | missense | RNFT1 | GRCh38.p7 | 17:59957277 | GACTCCATCTAGTTA[C/T]GTTACCAAACTCCCC | 51136 |
rs139402154 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954361 | TAATAGGATTTTGAA[A/G]GATTGTTAGATCTAC | 51136 |
rs139407842 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962189 | CATGCCCAGCCACTA[A/C]AAGTTTTTCATGATG | 51136 |
rs139462395 | snp | C/G/T | 6.59201e-05 | 0.00574078 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962904 | AGCCACTTGAAGAGA[C/G/T]AGCGGAATTCTGAGA | 51136 |
rs140037039 | in-del | -/A | 0.0130921 | 0.0798413 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959433 | TCCCATTTGACATGG[-/A]AGACTTATCAGCTAC | 51136 |
rs140111904 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954699 | AGTGCAATATGAAGA[A/C]GACTTAGGGACCACT | 51136 |
rs140131960 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959735 | ACCAACATGGTGAAA[C/T]TCCGTCTCTATTAAA | 51136 |
rs140134307 | in-del | -/T | 0.0865458 | 0.189163 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952033 | TAATTATAAGGGCAA[-/T]TTTTTTATAAGATTT | 51136 |
rs141254111 | snp | A/G | 0.000216071 | 0.0103918 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59958351 | GCATTTTAAGCCCAT[A/G]AAAAAGAATTTCAGA | 51136 |
rs141412497 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953903 | GACAAAACTTAGCCA[A/G]TCCACTAGTATGTAC | 51136 |
rs141521142 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959753 | CGTCTCTATTAAAAA[C/T]ACAAAAATTTGCCAG | 51136 |
rs142057142 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955992 | TTTCATGCCATGAAC[A/G]TATTTATGCACATAT | 51136 |
rs142118872 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956999 | ACTTAGATAATCCAC[A/G]CTATGTGAAGGTCGA | 51136 |
rs142157351 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963764 | ATCTTAATGCCTTAT[C/T]ATCATCATAGGTAAC | 51136 |
rs142393490 | snp | A/G | 3.29647e-05 | 0.00405971 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963205 | TTCCTGGAGGACTGT[A/G]CAGTTGGCTACGATT | 51136 |
rs142527640 | in-del | -/AAC | 0.079617 | 0.182947 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963738 | AATGTTAGGAAAAAA[-/AAC]AACATTAAATCTTAA | 51136 |
rs142631280 | snp | A/G | 0.000399208 | 0.0141225 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962564 | AACCTGATTTACAAT[A/G]CTTTTGTTTGCATAC | 51136 |
rs143076700 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959271 | AACCCAGAGGTCATT[C/T]TTGCTTCTCTCCACC | 51136 |
rs143220868 | in-del | -/TGTT | 0.00358779 | 0.0422022 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952237 | ATCAAGTAAGCCAGC[-/TGTT]TGTTTATAATCCACA | 51136 |
rs143267390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953695 | AACTGCTTAAGGTCT[C/T]TGAGTTACTAGTAAC | 51136 |
rs143920413 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953629 | CTGGCTGTACCATCC[A/G]TTTAACCATAAAAGC | 51136 |
rs144047944 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955474 | TTTGTCTCAGAGAAA[C/G]AATATCAGGGTATTT | 51136 |
rs144449093 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961566 | TTATGGAAAAATTCC[C/T]TGGGTTTCATTTTCT | 51136 |
rs144923460 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955632 | AGAAACAAGCTTGCA[C/T]AGGATGTAGCAAAGT | 51136 |
rs145297792 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962422 | ATAACGTGGATGTTA[C/T]AATATATCCTATTAC | 51136 |
rs145623665 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952468 | CACTTAGAAAATGTT[A/C]CTGATAAAATACAAC | 51136 |
rs146036461 | snp | C/T | 0.000348788 | 0.0132012 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962854 | GCATAACAAGTTTGA[C/T]GCTCAGAATCAAAAT | 51136 |
rs146129677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954666 | CCAGTAATCTATTAT[C/T]TGAAAGGTCTCCAAG | 51136 |
rs146256947 | snp | A/C/G | 0.000199855 | 0.00999449 | missense | RNFT1 | GRCh38.p7 | 17:59958376 | TTCAGAATGAAGTCT[A/C/G]TAATTCCAACAATCC | 51136 |
rs146980146 | snp | C/T | 0.000869013 | 0.0208267 | missense | RNFT1 | GRCh38.p7 | 17:59953108 | ACTCTTCACAAAATA[C/T]ATGCTGTAATGGAAT | 51136 |
rs147000393 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956798 | TACAACTATGTCAAA[A/G]TCAAAGCAATTTTAT | 51136 |
rs147210508 | in-del | -/TTAAATTAAATT | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960462 | AAAAAAAAAAGAAAA[-/TTAAATTAAATT]AAAAAAAAAAAAAAG | 51136 |
rs147486826 | in-del | -/A | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952609 | TCTTAAAATATTATG[-/A]AAAATATTCTTTATT | 51136 |
rs147639974 | snp | A/G | 0.000148296 | 0.00860964 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962908 | ACTTGAAGAGATAGC[A/G]GAATTCTGAGAAGGA | 51136 |
rs148624672 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955703 | TGGCCAGTTAGTCTC[C/G]TTTACTTTGTAGACA | 51136 |
rs149359685 | snp | A/T | 0.0887219 | 0.191022 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957782 | CCCAGGAGGCGGAGG[A/T]TGCAGTGAGCCAAGA | 51136 |
rs149674591 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960389 | AATACAAGTTTCTTC[A/T]CTGTATGAAAAACAT | 51136 |
rs149985376 | snp | C/T | 9.8837e-05 | 0.00702914 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962934 | AAGGAGCTACTACCA[C/T]GATCTCCAGATTCTG | 51136 |
rs150231220 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957093 | ATTTCTAAACAAATA[C/T]AGAACCTGCTATTAC | 51136 |
rs150420204 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964982 | TCCGAGATCCTGGGC[C/G]TTTTGAGGTTAAAAA | 51136 |
rs150547108 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959800 | CTGTAATCCCAGCTA[C/T]TCAGGAGGCTTAGAC | 51136 |
rs150771523 | in-del | -/AATA | 0.356597 | 0.226135 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960918 | AGATTATAAGAATTT[-/AATA]AATTAATGTTTTAAT | 51136 |
rs150915376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954305 | AGCCATATACAGAAC[C/T]ACCTCTTGAGTGCAC | 51136 |
rs151231823 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956279 | AACAATTAGCAGGTG[A/G]TTGTCAATGTGTGAT | 51136 |
rs151281621 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963946 | TAGATACTTTGGAGA[G/T]TCACCACGTAATTGC | 51136 |
rs181074229 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955517 | TTCGGCACAAATCTT[A/C]CAAGACCAATTATAG | 51136 |
rs181123072 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960335 | GTTTTATACTACTTT[A/T]GTGACCAAACAGAAC | 51136 |
rs181319780 | snp | A/C | 0.0146672 | 0.084371 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954978 | ATGTGATGTCAATAA[A/C]CCTCAGTGAAATTTG | 51136 |
rs181665408 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961628 | TGTCGCCAGGCTGGA[A/G]TGCAGTGGCACAATC | 51136 |
rs181727456 | snp | A/G | 0.0166325 | 0.0896639 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965509 | TGTAATCCCCGCTAC[A/G]GATACTCGGGAAGCT | 51136 |
rs181758000 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966174 | CGCCTGTAATCCCAG[C/T]TACTCGGGAGGCTGA | 51136 |
rs181936008 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956117 | ATTTTCACAGGTGAA[C/T]AAGGAGTTAATAGGA | 51136 |
rs182232915 | snp | A/C | 0.00119737 | 0.0244387 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952015 | AAACTTTTATGGAGA[A/C]GACTAATTATAAGGG | 51136 |
rs182433059 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953225 | ATGGAGACTGAAGTC[C/T]TGCTCTGTCACCCAG | 51136 |
rs182450357 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961004 | CAAGCATTCTTCCCA[A/G]CTCAGCCTCCCAAGT | 51136 |
rs182723562 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966692 | TGGCCAGATACTACG[A/G]TTCATTCCTATAATC | 51136 |
rs182736636 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962274 | AATCAGATCAGATAC[C/T]GTGTTCTAACTCTTT | 51136 |
rs182836451 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956785 | TGATCAAGACAAATA[C/G]AACTATGTCAAAGTC | 51136 |
rs182854039 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961761 | TTTGTGTTTTTAGTA[G/T]ACATGGGGTTTCACC | 51136 |
rs182884489 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957803 | TGAGCCAAGATCACA[A/C]CACTGCACTCCAGCC | 51136 |
rs183609874 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953967 | TTTTTTTTTTGCCTT[A/C]CAGCAAACATAAATT | 51136 |
rs183827874 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952479 | TGTTACTGATAAAAT[A/G]CAACATTTAGAATTT | 51136 |
rs184288755 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955315 | ATTTAGCAAAGTACA[C/T]TTGCAGATAATTATG | 51136 |
rs184469367 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965199 | GAGAGGTGCGGAGAG[C/T]CTGCGTGGGGTGGAA | 51136 |
rs184498716 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960590 | CCAAGGTCGGCGGAT[C/T]GCTTGAGGTCAGGAG | 51136 |
rs184514898 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958753 | GCTGTGTTTTTCTTA[A/C]CCAATTCCAATCAGG | 51136 |
rs184610285 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964242 | TCTGTGTCATTCTAT[C/T]TCACTCCCAGGACTG | 51136 |
rs185157564 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966700 | TACTACGGTTCATTC[C/G]TATAATCCTAGCACT | 51136 |
rs185294036 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954749 | GGTCTAAAAATTATT[C/T]GAAATTATAAAAAGC | 51136 |
rs185389493 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59951923 | AGGCGAACAAACCAC[A/G]CTATCAAAACCTCAT | 51136 |
rs185412992 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958145 | CAAGTGCCTGAACAA[A/T]TGGTTGCTAAGCTGA | 51136 |
rs185703177 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961669 | GCAACCTCTGCCTCC[C/T]GGGTTCAAGCAATTC | 51136 |
rs185926847 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955618 | TATGTCTTGTCTAGA[A/G]AAACAAGCTTGCATA | 51136 |
rs185948776 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965770 | CCAAGGCGGGTGGAT[C/T]ACAAGGTCAAGAGAT | 51136 |
rs186471738 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966234 | GGAGGTTGCAGTGAG[C/T]TGAAATCGTGCCACT | 51136 |
rs186713043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953886 | ATTATCAGAACATAA[A/G]GGACAAAACTTAGCC | 51136 |
rs187052946 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956168 | TGGATTAAAAAAGAG[C/G]AACACAATTTCATAA | 51136 |
rs187116249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956833 | TTCACCTGTTTTTAA[C/T]ATTTAGATTTTAAAG | 51136 |
rs187359173 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961190 | TACAGGCACGTGCCA[C/T]CACGCCCAGCTAATT | 51136 |
rs187439271 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957812 | ATCACACCACTGCAC[C/T]CCAGCCTGGGCAACA | 51136 |
rs187578879 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952057 | AAGATTTTAGGGCAT[C/T]TGTCTTGAAACTTTT | 51136 |
rs187916935 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961811 | CAAACTTCTGACCTC[A/G]GGTGATCTGCCTGCC | 51136 |
rs188071198 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962447 | TATTACTTCCTATTT[C/G]TTTCAAGTTATTTCC | 51136 |
rs188223356 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952675 | CTAAAACCACTAGTT[C/T]TAATTTCAAATTGCT | 51136 |
rs188582642 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955470 | GTAGTTTGTCTCAGA[C/G]AAAGAATATCAGGGT | 51136 |
rs188804297 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965898 | CGGGAAGCTGAGGCA[A/G]GAGAATCGCTTGAAC | 51136 |
rs188842766 | snp | A/C | 0.00339935 | 0.0410867 | missense | RNFT1 | GRCh38.p7 | 17:59960077 | AATTACCTGTAATAA[A/C]GTGACTGAGAATGAA | 51136 |
rs189061049 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960854 | AGAAAATTTCAAAAT[A/G]CATTTTAACCTTGAC | 51136 |
rs189353481 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965340 | AAACGAAGTTTAGGT[C/T]GGGCGCAGTGGCTCA | 51136 |
rs189704134 | snp | C/T | 0.00119737 | 0.0244387 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59951954 | GACCACCTCTCAGTG[C/T]GAGCTTCAATCTTCC | 51136 |
rs189785570 | snp | G/T | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964856 | CACGGCTGCCGGGGT[G/T]TTTTGGCAGCGAGAA | 51136 |
rs189867373 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954802 | GTTTTACGGAGAAAC[C/T]GCAACTGTAAATGTC | 51136 |
rs190063120 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957617 | CCAGCACTTTGGGAT[G/T]GGCAGATCACCTGAG | 51136 |
rs190115681 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961738 | AGCGCCACCACGCCC[A/C]GCTAATTTTTGTGTT | 51136 |
rs190366614 | snp | A/C/G | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956352 | GCCCCAAGTGCCAAA[A/C/G]TACTAGAAAATAATC | 51136 |
rs190792043 | snp | C/T | 5.49707e-05 | 0.00524236 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954042 | ATTTAAAAATGTAAT[C/T]ACCTGACAAATGAGA | 51136 |
rs190811376 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961455 | ATGCATGATACTTTA[A/C]ACAGACATAGCCATT | 51136 |
rs190905906 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962011 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGAATAC | 51136 |
rs191400803 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966545 | TTAGGAAACAGGAAA[A/T]AAAACAGAATATAAC | 51136 |
rs191420973 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953924 | TAGTATGTACCCTGA[A/C]TGCTACCTTCCACTA | 51136 |
rs191696568 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952808 | ATATATATTTTAAAA[C/T]ACAGGGTGGTTTCAT | 51136 |
rs191962499 | snp | C/T | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952247 | GCCAGCTGTTTATAA[C/T]CCACATGAATTATTT | 51136 |
rs192344924 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955819 | AATTGAGAATCAAAC[A/C]CTGAAGTCTGCTGAC | 51136 |
rs192435044 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964928 | AAATAATAAGTCGTT[A/G]TTATGTGTTATGTAT | 51136 |
rs192496107 | snp | A/G | 5.04096e-05 | 0.00502018 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962832 | TATGTCCTACCTGTT[A/G]TATGCTGCATAACAA | 51136 |
rs192962127 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964219 | CTAGAGTTAACGTCA[A/G]GGAATGTTCTGTGTC | 51136 |
rs193019850 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954369 | TTTTGAAAGATTGTT[A/G]GATCTACTAGCTTTA | 51136 |
rs193274795 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958110 | TTCTGATTTTATCCA[A/G]ATAGGTTAATAATCA | 51136 |
rs199530443 | snp | C/G/T | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963018 | CTGTGTACACATCCA[C/G/T]GGGCACAGCTATGGA | 51136 |
rs199598962 | snp | C/T | 0.000293541 | 0.0121113 | stop-gained | RNFT1 | GRCh38.p7 | 17:59957374 | TTCTAAAAGCATATA[C/T]CAGTAACCCTAAAAA | 51136 |
rs199982924 | in-del | -/TC | 0.0225045 | 0.103662 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954279 | CAAAGGATACAAACA[-/TC]TCAAAGCTGAGCCAT | 51136 |
rs200011393 | in-del | -/A | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966541 | CATTTAGGAAACAGG[-/A]AAAAAAAACAGAATA | 51136 |
rs200039301 | snp | A/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960921 | TTATAAGAATTTAAT[A/T]AATTAATGTTTTAAT | 51136 |
rs200047998 | snp | A/G | 0.00048162 | 0.0155106 | missense | RNFT1 | GRCh38.p7 | 17:59953081 | TCTCTCTGTTAAACC[A/G]TAAGGTCATGCACTC | 51136 |
rs200050289 | snp | A/C | 0.00453086 | 0.0473804 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964653 | GGGAGCGACAGCAAG[A/C]ACAGCGGCATACACC | 51136 |
rs200144344 | snp | A/T | 1.81731e-05 | 0.00301433 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963323 | TCTAAGTAAACAGGC[A/T]GTTAAATACCAGCAG | 51136 |
rs200320106 | snp | C/T | 4.98848e-05 | 0.00499399 | missense | RNFT1 | GRCh38.p7 | 17:59952983 | TTATACAACTTAATA[C/T]ATTTGAAGGTGTGAT | 51136 |
rs200452189 | snp | C/T | | | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963006 | CCCCGTAAGCGACTG[C/T]GTACACATCCATGGG | 51136 |
rs200572570 | snp | A/G/T | 1.67424e-05 | 0.00289326 | missense | RNFT1 | GRCh38.p7 | 17:59954118 | TCCACATCTGAACAC[A/G/T]GTCTCTTGCTGGCAG | 51136 |
rs200661534 | snp | C/T | | | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963058 | TTATATTTCTGGAGC[C/T]TGCATTTTCTGCACA | 51136 |
rs200915307 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959915 | ACTCCGTCTCAAAAA[A/G]AAAAAAAAAAAAAAA | 51136 |
rs201302517 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953558 | TGTGAAAATGGAGAA[C/T]GTATGAGACATTCAA | 51136 |
rs201329824 | snp | A/G | 3.35497e-05 | 0.00409558 | missense | RNFT1 | GRCh38.p7 | 17:59957354 | CGGTAGTATTGACAC[A/G]ATTCTTCTAAAAGCA | 51136 |
rs201386625 | in-del | -/A | 0.00795532 | 0.062565 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966287 | GGAGACCCCCACCTC[-/A]AAAAAAAAACACATT | 51136 |
rs201457312 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960457 | AAAAAAAAAAAAAAA[A/G]AAAATTAAATTAAAT | 51136 |
rs201837426 | snp | C/T | 1.69648e-05 | 0.00291241 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957191 | AATCATTAATGTGAA[C/T]CATGCAGTGACAAGA | 51136 |
rs201862459 | in-del | -/AGGT | 0.0314385 | 0.121371 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952647 | AATGTCAGGAAAGAA[-/AGGT]TACCTGAGTTCTCTA | 51136 |
rs201932517 | snp | C/T | 0.000399281 | 0.0141238 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963037 | CACAGCTATGGACAC[C/T]TGACCTTATATTTCT | 51136 |
rs201992757 | snp | A/G | 4.97418e-05 | 0.00498682 | missense | RNFT1 | GRCh38.p7 | 17:59957310 | AGCTTATAAGGTAGC[A/G]AAACCAAACTGGTAT | 51136 |
rs367607184 | snp | A/G | 0.000217462 | 0.0104252 | missense | RNFT1 | GRCh38.p7 | 17:59954116 | CATCCACATCTGAAC[A/G]CTGTCTCTTGCTGGC | 51136 |
rs367619232 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956377 | ATAATCAAAGTAAAA[-/G]AAAAGGATCATCTAT | 51136 |
rs367793075 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953991 | ATAAATTTGACTTTT[C/G]CAAGTCACAGAGAAC | 51136 |
rs368224728 | snp | A/G | 1.6775e-05 | 0.00289607 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59960097 | CTGAGAATGAAAGGT[A/G]TAATATAAAAGAACA | 51136 |
rs368407775 | snp | A/G | 1.65272e-05 | 0.0028746 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963222 | AGTTGGCTACGATTG[A/G]CTTGCATGGCCCTTA | 51136 |
rs368418433 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961529 | TCCCAATGATTTATA[C/T]GACGGGCTCGTGTAA | 51136 |
rs368504306 | snp | C/T | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964728 | GCTCTTCTCTCAGCC[C/T]GGCGGCAACGGCGGC | 51136 |
rs368539310 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960812 | AGCAAAACACCGTCT[C/T]AGAAAAAAAATGGAC | 51136 |
rs368746369 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958793 | CTTCCTTTCAATGAA[C/T]TGCTTGTCAAGATCA | 51136 |
rs368817922 | snp | A/C/G | 0.00013793 | 0.00830346 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954158 | AACTCTATGAAGATA[A/C/G]TAAGTTCTGTTCATC | 51136 |
rs369039672 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955581 | AACTGACTTGGACAA[A/C]GCTGAACTCTCTGAA | 51136 |
rs369146360 | snp | C/T | 0.000238591 | 0.0109196 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957406 | TAAGAAGAAAACAAA[C/T]AGAGCTACCCAAACT | 51136 |
rs369251713 | snp | C/T | 1.66388e-05 | 0.00288429 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962579 | GCTTTTGTTTGCATA[C/T]ATAAAAGTTGTTAGC | 51136 |
rs369331866 | snp | G/T | 1.66239e-05 | 0.00288299 | missense | RNFT1 | GRCh38.p7 | 17:59957237 | ACTTTTAATATGAGG[G/T]AGAGTAAAGCCAGCA | 51136 |
rs369394949 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963424 | TTATTTATCACTGGA[C/T]TCCTCCCTTCTCCCT | 51136 |
rs369549123 | snp | A/C | 3.3269e-05 | 0.00407841 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962560 | GAAAAACCTGATTTA[A/C]AATGCTTTTGTTTGC | 51136 |
rs369629097 | snp | G/T | 5.37774e-05 | 0.00518515 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956457 | TGAAGAAAGGTGAAG[G/T]TGTTTTTCTTAACTG | 51136 |
rs369728613 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965719 | GCTGAGGAGGGGAGT[A/G]GTAGCTCACACCTGT | 51136 |
rs369800916 | in-del | -/TC | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953189 | GGGAATGAAAGGGAT[-/TC]TTTTTTTTTTTTTTT | 51136 |
rs369886171 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956994 | TCCCTACTTAGATAA[C/T]CCACGCTATGTGAAG | 51136 |
rs370072222 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953604 | TATGATTGGTAGAGC[A/C]ACTAGTGTTCTGGCT | 51136 |
rs370126242 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964198 | TCCCGTTTGTCTAGG[A/G]GGAGGCTAGAGTTAA | 51136 |
rs370273345 | snp | A/G | 0.00198071 | 0.0314075 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964713 | CCGCAAACCCCGCAA[A/G]CTCTTCTCTCAGCCC | 51136 |
rs370354835 | snp | C/T | 0.000365012 | 0.0135045 | missense | RNFT1 | GRCh38.p7 | 17:59953065 | CAGAGTGGACATGTT[C/T]TCTCTCTGTTAAACC | 51136 |
rs370573890 | snp | A/G | 1.67284e-05 | 0.00289205 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59958414 | TTCCCAGAAGCTCAA[A/G]TGGTCCAAAGTAGGA | 51136 |
rs370635093 | snp | A/G | 1.64746e-05 | 0.00287002 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962924 | GAATTCTGAGAAGGA[A/G]CTACTACCATGATCT | 51136 |
rs370678420 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959014 | CACTCTCTTTCCTGG[A/G]TTAGTTTTGTCCAGT | 51136 |
rs370716818 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954515 | GAGCTTATTACCTGC[A/G]GCAGTGGTTCATAAA | 51136 |
rs370805016 | snp | C/T | 3.90617e-05 | 0.0044192 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957431 | CAAACTACTTAACTA[C/T]ATAGCACAAACAATA | 51136 |
rs371211205 | snp | C/G | 4.6503e-05 | 0.00482176 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954011 | TCACAGAGAACTGTT[C/G]TATTTAGGTTTTTAA | 51136 |
rs371329324 | snp | C/T | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952295 | TACTCCATGGTACTA[C/T]ACAAAAAGCATGATC | 51136 |
rs371887988 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957012 | ACGCTATGTGAAGGT[A/C/T]GACTCCCCTTCCCTC | 51136 |
rs371935736 | snp | C/G | 0.000102138 | 0.00714553 | splice-donor-variant | RNFT1 | GRCh38.p7 | 17:59956487 | GATAAAAAGTACTTA[C/G]TGGTTGTGTAAAAAA | 51136 |
rs372089614 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957409 | GAAGAAAACAAATAG[A/G]GCTACCCAAACTACT | 51136 |
rs372110461 | in-del | -/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953190 | GGAATGAAAGGGATT[-/C]TTTTTTTTTTTTTTT | 51136 |
rs372176705 | in-del | -/CT | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955592 | ACAAAGCTGAACTCT[-/CT]GAATTTTATTATGTC | 51136 |
rs372333129 | snp | A/G | 0.000149831 | 0.00865409 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59960127 | AGAAGATCCTGCTAA[A/G]AATACCAGTAACCAA | 51136 |
rs372389096 | snp | A/C | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966057 | TTTGGAAGGCCGAGG[A/C]GGGAGGATCACTTGA | 51136 |
rs372449596 | snp | G/T | 0.000534976 | 0.0163463 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954159 | ACTCTATGAAGATAG[G/T]AAGTTCTGTTCATCT | 51136 |
rs372456221 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954793 | CATAAAAAAGTTTTA[C/T]GGAGAAACTGCAACT | 51136 |
rs372482036 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953775 | TGTTCTACATGGCTA[A/G]TATCCAATTATAAAA | 51136 |
rs372522671 | snp | G/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966045 | TAATCCCAGCGCTTT[G/T]GAAGGCCGAGGCGGG | 51136 |
rs372745973 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963495 | GGGAACATTTGCACC[-/A]AAAAAAAAAAAGTTG | 51136 |
rs372799912 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961063 | CTTTTTTGAGACTGG[A/G]TCTCACTCTTTCACC | 51136 |
rs372897436 | snp | A/C/G/T | 0.00128951 | 0.0253611 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964691 | GCCCTTCAGTCGGGG[A/C/G/T]CATCAACCGCAAACC | 51136 |
rs373016769 | snp | G/T | 1.68374e-05 | 0.00290145 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962830 | ATTATGTCCTACCTG[G/T]TATATGCTGCATAAC | 51136 |
rs373021222 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959621 | ATCTGAGTAAGTCAC[C/T]TAAAGCTCTCACTTA | 51136 |
rs373057504 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965022 | TTGGAGAACCTACCC[C/G]TGGAGGAGTGTTAGG | 51136 |
rs373188552 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965056 | TCCGGGCTCGGATGT[C/T]CGCGAGCTTGACGCC | 51136 |
rs373282555 | snp | A/C | 6.58913e-05 | 0.00573945 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962944 | TACCATGATCTCCAG[A/C]TTCTGCGGCAGTATC | 51136 |
rs373337646 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957070 | AGATAGTCTATTTCC[A/G]TTTCTCCATTTCTAA | 51136 |
rs373370452 | snp | C/T | 1.66125e-05 | 0.00288201 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59953082 | CTCTCTGTTAAACCA[C/T]AAGGTCATGCACTCT | 51136 |
rs373406435 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956275 | CTGCAACAATTAGCA[A/G]GTGGTTGTCAATGTG | 51136 |
rs373785398 | snp | A/C | 8.43583e-05 | 0.006494 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952941 | CATTATGACCAAATG[A/C]CATTAGTATTTTGTG | 51136 |
rs373791809 | snp | C/T | 0.000165986 | 0.00910854 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59954120 | CACATCTGAACACTG[C/T]CTCTTGCTGGCAGCC | 51136 |
rs374047009 | snp | C/T | 1.67022e-05 | 0.00288978 | missense | RNFT1 | GRCh38.p7 | 17:59954107 | AACAAATATCATCCA[C/T]ATCTGAACACTGTCT | 51136 |
rs374226039 | in-del | -/A | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963739 | TGTTAGGAAAAAAAA[-/A]CAACATTAAATCTTA | 51136 |
rs374411211 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954370 | TTTGAAAGATTGTTA[C/G]ATCTACTAGCTTTAC | 51136 |
rs374695878 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955526 | AATCTTACAAGACCA[A/G]TTATAGTAAAATGGT | 51136 |
rs375025296 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963440 | TCCTCCCTTCTCCCT[-/T]AATGCCAAGGCTCTG | 51136 |
rs375346435 | snp | A/G | 3.35677e-05 | 0.00409668 | missense | RNFT1 | GRCh38.p7 | 17:59958424 | CTCAAATGGTCCAAA[A/G]TAGGATTTAAAAAAA | 51136 |
rs376044935 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960298 | AGAATATGTTAAACT[A/G]TACATAATCATCACA | 51136 |
rs376198298 | snp | C/G/T | 3.31863e-05 | 0.00407336 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962856 | ATAACAAGTTTGACG[C/G/T]TCAGAATCAAAATAT | 51136 |
rs376215881 | snp | C/T | 0.0001156 | 0.00760176 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963219 | TGCAGTTGGCTACGA[C/T]TGGCTTGCATGGCCC | 51136 |
rs376278427 | snp | C/T | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962994 | CTGTGGGAGTGACCC[C/T]GTAAGCGACTGTGTA | 51136 |
rs376315656 | snp | C/T | 0.000211279 | 0.0102759 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954174 | TAAGTTCTGTTCATC[C/T]ACAAATTTCTTTCTT | 51136 |
rs376511641 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957185 | ATCAGTAATCATTAA[C/T]GTGAATCATGCAGTG | 51136 |
rs376591518 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963812 | CTTAGGTGACCTACA[A/C]ATTAGATTTTCTGCT | 51136 |
rs376771900 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961709 | AGCCTCCCAAGTAGC[C/T]GGGACTACAGGCAAG | 51136 |
rs376898864 | snp | C/G | 1.69833e-05 | 0.00291399 | missense | RNFT1 | GRCh38.p7 | 17:59956489 | TAAAAAGTACTTACT[C/G]GTTGTGTAAAAAATA | 51136 |
rs376901171 | snp | A/G/T | 7.05492e-05 | 0.00593882 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964693 | CCTTCAGTCGGGGCC[A/G/T]TCAACCGCAAACCCC | 51136 |
rs376936665 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958683 | CTTCACGGTTTGTCA[C/T]AGTTGACACCTTTCT | 51136 |
rs376973552 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966218 | CTTGAACCCAGGTGG[C/T]GGAGGTTGCAGTGAG | 51136 |
rs377335560 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959739 | ACATGGTGAAACTCC[A/G]TCTCTATTAAAAATA | 51136 |
rs397856980 | in-del | -/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953206 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGACTGAA | 51136 |
rs527562328 | in-del | -/T | 0.299664 | 0.245017 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961033 | TAGTTGTAATCTCCC[-/T]TTTTTTTTTTTTTAC | 51136 |
rs527671735 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962425 | ACGTGGATGTTACAA[G/T]ATATCCTATTACTTC | 51136 |
rs528153860 | snp | G/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964289 | CCGTGTCTGGCGGTT[G/T]GGGTTTCAGTGCTTT | 51136 |
rs528599074 | snp | A/G | 8.48011e-05 | 0.00651102 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956561 | TCCAAAAGCTGAAAA[A/G]AGAAATAAGAGATCA | 51136 |
rs528661751 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964799 | GCCCTGCCCCGGCTC[C/T]ACCTCCTAGCCCCGC | 51136 |
rs528729909 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964485 | TTCAACACAACTCTT[C/T]CGGAATCTCCGAGGG | 51136 |
rs529296171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956424 | TGTAAAACTGCTGAA[C/T]TAAAAAAATTTTTGC | 51136 |
rs529356689 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955768 | GTTGGCATTCTTTTA[A/C]GTCAGTCTCCTTGGG | 51136 |
rs529356779 | snp | C/G | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964745 | GCGGCAACGGCGGCG[C/G]CGCGCGCGCTCCCCG | 51136 |
rs529420533 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964313 | GTGCTTTTCACTAAA[G/T]GCTTTCACCGAGGCC | 51136 |
rs529716038 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961435 | CTATAAATTTCCAGG[A/T]CAGAATGCATGATAC | 51136 |
rs529745612 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956045 | CTCCAGTAAGAAAAC[C/T]GCAAGAGACATGATT | 51136 |
rs529861787 | in-del | -/AG | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965608 | TCCAGCCTGGGCAAC[-/AG]AGTGAGTGAGACTCG | 51136 |
rs530281527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958197 | AGTTAGCAAACTGAA[A/G]AACTGCAAAAGGAGG | 51136 |
rs530350924 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957711 | TTAACTGGGTGTGGT[G/T]GTGGGCACCTGTAAT | 51136 |
rs530384655 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959889 | CACTCCAGGCTGGGC[A/G]AGAGAGTGAGACTCC | 51136 |
rs530574898 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959525 | CTTTAAAAATACGAA[A/G]TATGTAAACAAAAAC | 51136 |
rs531063940 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965861 | CCGGGTGTGGTGGTG[A/C]GTGCCTGTAATCTCA | 51136 |
rs531126856 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964924 | CGCTAAATAATAAGT[C/T]GTTGTTATGTGTTAT | 51136 |
rs531189452 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956650 | ACATCAAATCCTCAT[A/G]TTAACTTAATGTTCA | 51136 |
rs531454543 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962412 | CAAATTTAACATAAC[A/G]TGGATGTTACAATAT | 51136 |
rs532054461 | in-del | -/TACTC | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956905 | GAGAACAGGACAAGA[-/TACTC]TACTAGTTTAAGAAT | 51136 |
rs532069835 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953944 | ACCTTCCACTAAACA[C/G]TAGATTTTTTTTTTT | 51136 |
rs532254134 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953229 | AGACTGAAGTCTTGC[G/T]CTGTCACCCAGGCCG | 51136 |
rs532261329 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960580 | CTTTGGGAGGCCAAG[C/G]TCGGCGGATCGCTTG | 51136 |
rs532318166 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961501 | GTGAAATTTTAGAAA[C/T]TCATCCTCTTTTTCC | 51136 |
rs533077245 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954601 | TAAAAATAGATTTCT[C/T]TGTTCCACACAATAT | 51136 |
rs533180725 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964762 | GCGCGCGCTCCCCGG[A/G]CGTTCTCACGCGCGC | 51136 |
rs533421595 | snp | C/T | 3.43542e-05 | 0.00414439 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963282 | GCTTCAGGCCTCTGT[C/T]TCCTAAAAAATCAAA | 51136 |
rs533975268 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952695 | TTCAAATTGCTGTTT[G/T]GGTAACATAAAGAAA | 51136 |
rs534308299 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961131 | AGCCCCAACCACCTG[C/G]GGTCAGGCAATCCTC | 51136 |
rs534426420 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956851 | TTAGATTTTAAAGTT[C/T]CATAAAGTGATTATT | 51136 |
rs534543737 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960411 | GAAAAACATTACCTA[G/T]GTTTCAAAGAAGCCA | 51136 |
rs534722513 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966067 | CGAGGCGGGAGGATC[A/G]CTTGAGGTCAGGAGT | 51136 |
rs534806997 | in-del | -/AAG | 3.40032e-05 | 0.00412316 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956568 | GCTGAAAAGAGAAAT[-/AAG]AGATCATTTATTAAT | 51136 |
rs534950873 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955346 | CTGACAAGCTTTTAA[A/G]ACGTTACTCATCTGG | 51136 |
rs535208402 | snp | C/G | 9.39011e-05 | 0.0068514 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964597 | CTCTGCCCGCTTCCC[C/G]CAGGCCTAACCTCTC | 51136 |
rs535968292 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955244 | ATAAAGATTTCAGAA[A/G]TAAGTCAGGATACTG | 51136 |
rs536033499 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963525 | GAGCTGCAAATGCTT[C/T]CAGTTCTCTAATGGC | 51136 |
rs536043609 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954452 | ATCTGAAATGTAACT[A/G]TTATAAAATCTATAG | 51136 |
rs536104946 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962687 | ATAAGCTAACAATGA[C/T]ACAAATTAAAAATAA | 51136 |
rs536248006 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953332 | CCTCCCAAGTTGCCG[A/G]GATTACAGGTGACCA | 51136 |
rs536436005 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959713 | GATCACGAGGTCAGG[A/G]GGTCTGACCAACATG | 51136 |
rs536498904 | snp | A/C | 0.000173235 | 0.00930524 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958665 | ATAGAATAAGGAAAA[A/C]GTCTTCACGGTTTGT | 51136 |
rs537103775 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956175 | AAAAGAGGAACACAA[-/T]TTTCATAAGATTGTT | 51136 |
rs537158853 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958515 | AATAAAGGGTTTTAA[C/T]TTGCTACAAATATTT | 51136 |
rs537220038 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957832 | CCTGGGCAACAGAGC[A/C/G]AGAGACAATCTCAAA | 51136 |
rs537282631 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966191 | ACTCGGGAGGCTGAG[G/T]CAGGAGAATCCCTTG | 51136 |
rs537361728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956004 | AACGTATTTATGCAC[A/G]TATAATTGAGCAATG | 51136 |
rs537441154 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961277 | TCCTGGGCTCAAGCA[A/G]TCTGCCCATCTCAGC | 51136 |
rs537690934 | snp | C/T | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952792 | CATTAGGTTGAACAT[C/T]ATATATATTTTAAAA | 51136 |
rs537726969 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956027 | GAGCAATGGGGAAAT[A/C]TGCTCCAGTAAGAAA | 51136 |
rs537887416 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959861 | GTTGCAGTGAGCCAA[A/G]ATCAAGACACTGCAC | 51136 |
rs539025724 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964521 | TTCTCCACCCACGTC[C/T]GAGCCTCGAGTGCCT | 51136 |
rs539086574 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963800 | ATAAACACTGCACTT[A/G]GGTGACCTACAAATT | 51136 |
rs539396270 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955462 | TCCTCTCTGTAGTTT[G/T]TCTCAGAGAAAGAAT | 51136 |
rs540335124 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59951911 | ACAAATACCTAGAGG[C/T]GAACAAACCACACTA | 51136 |
rs540972650 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964171 | AGAGGCTATCCCACA[C/T]TGCCGTGCTTTTCCC | 51136 |
rs541200944 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956320 | GATCACAGAGATAAA[A/G]CTCCTAAATTATTAT | 51136 |
rs541263153 | snp | A/G | 6.98153e-05 | 0.00590786 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964690 | AGCCCTTCAGTCGGG[A/G]CCATCAACCGCAAAC | 51136 |
rs541282800 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961668 | TGCAACCTCTGCCTC[A/C]CGGGTTCAAGCAATT | 51136 |
rs541598563 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954829 | TGTCGCTTTGGTAGA[A/G]TAACTACTGTCAAAA | 51136 |
rs541755800 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954614 | CTCTGTTCCACACAA[C/T]ATCAATTCACTAGGA | 51136 |
rs542489414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953812 | GTTTTTTAATCACTT[C/T]GGTATTCAATCTGCC | 51136 |
rs542596390 | in-del | -/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954801 | AGTTTTACGGAGAAA[-/C]TGCAACTGTAAATGT | 51136 |
rs542693712 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957644 | TGAGGTCAGGAGTTC[A/G]AGACCAGCTGGCCAA | 51136 |
rs542750948 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964754 | GCGGCGGCGCGCGCG[C/T]TCCCCGGACGTTCTC | 51136 |
rs543042645 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965569 | AGGTGGAGTTTGTAG[A/T]GAGCCAAGATCGTGC | 51136 |
rs543352110 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956391 | AGAAAAGGATCATCT[A/T]TTTATGAAATCCATT | 51136 |
rs543863391 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964260 | ACTCCCAGGACTGAA[C/T]AGTGGTGCAGTCACC | 51136 |
rs544007708 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955333 | GCAGATAATTATGCT[C/G]ACAAGCTTTTAAGAC | 51136 |
rs544202591 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961320 | TGAGATTACAGGCAT[A/G]AGCCACTGTGCCTTG | 51136 |
rs544259792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960331 | TACTGTTTTATACTA[C/T]TTTAGTGACCAAACA | 51136 |
rs544311463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959225 | AACCCAATGAAATGA[C/T]ACCACCATCCAGCCA | 51136 |
rs544373075 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958126 | ATAGGTTAATAATCA[A/G]GTTCAAGTGCCTGAA | 51136 |
rs544648803 | snp | A/G | | | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963031 | CATGGGCACAGCTAT[A/G]GACACCTGACCTTAT | 51136 |
rs544760287 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960586 | GAGGCCAAGGTCGGC[A/G]GATCGCTTGAGGTCA | 51136 |
rs545176136 | snp | G/T | 1.66935e-05 | 0.00288903 | missense | RNFT1 | GRCh38.p7 | 17:59957225 | GTAATGTTACCTACT[G/T]TTAATATGAGGTAGA | 51136 |
rs545496631 | snp | A/G | 0.00143213 | 0.0267211 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962999 | GGAGTGACCCCGTAA[A/G]CGACTGTGTACACAT | 51136 |
rs545883828 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953945 | CCTTCCACTAAACAC[C/T]AGATTTTTTTTTTTT | 51136 |
rs546060361 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952803 | ACATTATATATATTT[G/T]AAAACACAGGGTGGT | 51136 |
rs546122182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961239 | GATGGGGTTTTGCCA[C/T]GTTGCCCAGGCTCGT | 51136 |
rs546398427 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964453 | AGACAAGAAAGAGGA[C/G]AAAAAAGGGAAGAAA | 51136 |
rs546477889 | snp | G/T | 1.66626e-05 | 0.00288635 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59960118 | TAAAAGAACAGAAGA[G/T]CCTGCTAAGAATACC | 51136 |
rs546660517 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953186 | GTAGGGAATGAAAGG[A/G]ATTCTTTTTTTTTTT | 51136 |
rs546722049 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952415 | ACTACAGAGAATAAT[A/G]CAATACTATAATGTA | 51136 |
rs546884408 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958211 | AAAACTGCAAAAGGA[G/T]GATTCATTTAAACAA | 51136 |
rs547112153 | in-del | -/TAA | 0.000485185 | 0.0155678 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962509 | ATGGAGAGAAACAGT[-/TAA]TAATTTTTTAGTTGC | 51136 |
rs547736586 | snp | A/G | 1.64966e-05 | 0.00287194 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963212 | AGGACTGTGCAGTTG[A/G]CTACGATTGGCTTGC | 51136 |
rs548013831 | snp | C/G | 1.79277e-05 | 0.00299392 | missense | RNFT1 | GRCh38.p7 | 17:59954045 | TAAAAATGTAATTAC[C/G]TGACAAATGAGAAGA | 51136 |
rs548073604 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953330 | AGCCTCCCAAGTTGC[C/T]GGGATTACAGGTGAC | 51136 |
rs548075040 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962418 | TAACATAACGTGGAT[A/G]TTACAATATATCCTA | 51136 |
rs548219658 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959917 | TCCGTCTCAAAAAGA[A/G]AAAAAAAAAAAAAGC | 51136 |
rs548732122 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960001 | TACTATGTGAAGTAA[A/G]ATACAAAGTGCTATG | 51136 |
rs548798179 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965010 | AAATGTTCAGGCTTG[A/G]AGAACCTACCCCTGG | 51136 |
rs549113866 | snp | A/G | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952030 | AGACTAATTATAAGG[A/G]CAATTTTTTATAAGA | 51136 |
rs549331242 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963658 | TGCAGTTTCATCTCT[A/G]ATGTAGATTCTACAT | 51136 |
rs549492628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955806 | GAAATGACTGCAAAA[C/T]TGAGAATCAAACCCT | 51136 |
rs549513295 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964446 | CATGCACAGACAAGA[A/G]AGAGGAGAAAAAAGG | 51136 |
rs549557913 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955291 | TCAATTTCCCTTCAG[C/T]AAGGTGTCATTTAGC | 51136 |
rs549939534 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952722 | GAAAACACATTTACA[A/G]TTTAACACTGCAGTT | 51136 |
rs549942368 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955138 | GTTATCTAAACTTCT[C/T]GTACTAAAACGTCTC | 51136 |
rs550013776 | in-del | -/CA | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961067 | TTTGAGACTGGGTCT[-/CA]CTCTTTCACCCAGAC | 51136 |
rs550360590 | snp | A/G | 1.72187e-05 | 0.00293412 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962655 | AATTGAAAGAAAAAA[A/G]AATCAAAGAGGATTA | 51136 |
rs550693577 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959673 | ACACCTGTAATCCCA[A/G]CACTTTAGGAGGTGG | 51136 |
rs550753999 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958561 | AAAATATGAGTTTGG[C/G]AGGATGTCAGAGTTC | 51136 |
rs550800064 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957613 | GCTCCCAGCACTTTG[C/G]GATGGGCAGATCACC | 51136 |
rs550859554 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956746 | AGCAAGCTGAAGTAC[A/G]TTTAAACACCTAGAG | 51136 |
rs551055049 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959521 | GGTACTTTAAAAATA[C/T]GAAATATGTAAACAA | 51136 |
rs551268933 | snp | C/T | 0.0150606 | 0.0854603 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965939 | GAGGTTGCAGTGAGC[C/T]GGGATTAGCCACTGC | 51136 |
rs551384774 | snp | C/T | 1.66665e-05 | 0.00288669 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59958381 | AATGAAGTCTGTAAT[C/T]CCAACAATCCAAAAT | 51136 |
rs551552840 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966141 | AAAATACAAAAATCA[C/G]CCGGGCTTGGTGGCG | 51136 |
rs551777289 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964492 | CAACTCTTCCGGAAT[A/C]TCCGAGGGCAGAGTT | 51136 |
rs551918359 | snp | C/T | 1.70974e-05 | 0.00292376 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956578 | GAAATAAGAGATCAT[C/T]TATTAATTCAAACAG | 51136 |
rs551979581 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964813 | CCACCTCCTAGCCCC[A/G]CCCCCGCACCGCGCC | 51136 |
rs552375323 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952567 | AAAGTCAATGCTGAA[A/C]AAAATTCTACTTTTA | 51136 |
rs552984486 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958673 | AGGAAAAAGTCTTCA[C/T]GGTTTGTCATAGTTG | 51136 |
rs553025695 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956675 | TGTTCATTATATGTC[A/G]CATCTAATCATTTTG | 51136 |
rs553286195 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957866 | AAACAAAACCAAAAA[A/T]AAAGATACAATGAGA | 51136 |
rs553347615 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966587 | ACAGCCACAATGCAG[C/T]ACCAATATGTATTAG | 51136 |
rs553442990 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954627 | AATATCAATTCACTA[C/G]GACCAGACATATTGG | 51136 |
rs553501769 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966219 | TTGAACCCAGGTGGC[A/G]GAGGTTGCAGTGAGC | 51136 |
rs553680386 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963732 | GTTGGAAATGTTAGG[A/G]AAAAAAACAACATTA | 51136 |
rs553779850 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953449 | CAGGTGATCCACCCA[C/T]CTCAGCCTCCCAAAG | 51136 |
rs554499019 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952669 | AGTTCTCTAAAACCA[C/T]TAGTTCTAATTTCAA | 51136 |
rs554545627 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961023 | AGCCTCCCAAGTAGT[C/T]GTAATCTCCCTTTTT | 51136 |
rs554560926 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962087 | AGACAGGGTTTCACC[A/G]TGTTAGCCAGGATGG | 51136 |
rs554564429 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961046 | CCCTTTTTTTTTTTT[C/T]ACTTTTTTGAGACTG | 51136 |
rs554974721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956820 | CAATTTTATCTGATT[C/T]ACCTGTTTTTAACAT | 51136 |
rs555329156 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952268 | TGAATTATTTTAATA[A/G]TTACTTCGAGATACT | 51136 |
rs555762487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964525 | CCACCCACGTCCGAG[A/C]CTCGAGTGCCTATTC | 51136 |
rs556026739 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954351 | AAATAATACATAATA[C/G]GATTTTGAAAGATTG | 51136 |
rs556077851 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962754 | ACTGGATGCATTAAG[G/T]AGATTACCAATAATG | 51136 |
rs556566271 | in-del | -/AA | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956568 | GCTGAAAAGAGAAAT[-/AA]GAGATCATTTATTAA | 51136 |
rs556818345 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59961968 | TCAGCTCACTGCAAC[C/T]TCCACCTCCCAGGTT | 51136 |
rs556881380 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961255 | GTTGCCCAGGCTCGT[C/T]TTCAATTCCTGGGCT | 51136 |
rs557214298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957846 | CGAGAGACAATCTCA[A/C]AACAAAACAAAACCA | 51136 |
rs557277544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956937 | AATTATGTGTATGAC[A/G]ATGTTACTGTTGAGG | 51136 |
rs557338809 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965424 | AGGAGGTAGAGACCA[G/T]CCTGGCCAACATGGT | 51136 |
rs557527166 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953244 | TCTGTCACCCAGGCC[A/G]GAGTGCAATGGCACC | 51136 |
rs557555575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957810 | AGATCACACCACTGC[A/G]CTCCAGCCTGGGCAA | 51136 |
rs557754493 | snp | C/T | 3.5274e-05 | 0.00419949 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964694 | CTTCAGTCGGGGCCA[C/T]CAACCGCAAACCCCG | 51136 |
rs557996270 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965215 | CTGCGTGGGGTGGAA[C/G]TAGAAGTTAGAGTTG | 51136 |
rs558720907 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956258 | GTTCAAATATATAAG[C/T]ACTGCAACAATTAGC | 51136 |
rs558878310 | snp | C/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965739 | CTCACACCTGTAATC[C/G]CAGCACTTTGGGAGG | 51136 |
rs559571339 | snp | A/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965616 | GGGCAACAGAGTGAG[A/T]GAGACTCGGTCTCAA | 51136 |
rs559862404 | snp | A/G | 1.69063e-05 | 0.00290738 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956556 | AAAATTCCAAAAGCT[A/G]AAAAGAGAAATAAGA | 51136 |
rs560169802 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962220 | ATGGTCTTACTTACT[A/G]TGGTCAAAGTAACTG | 51136 |
rs560601185 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959389 | ACCAGGTCTTCTAAT[A/G]TTCTAATAAAAGCTG | 51136 |
rs560752955 | snp | C/G | 1.69169e-05 | 0.00290829 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960060 | TGTGTATTTGGACCT[C/G]TAATTACCTGTAATA | 51136 |
rs560879545 | snp | A/G | 1.65883e-05 | 0.00287991 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958267 | GATAACATCACTCCA[A/G]TAAAGCATAAGTGAG | 51136 |
rs560885486 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952178 | GATTACAGGTGTGAG[A/C]CACCATGCCTGGCCA | 51136 |
rs560885546 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961406 | TTAAGATTTTTCTAG[C/T]TTGATAGGTTTAACT | 51136 |
rs561036307 | snp | A/C | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952068 | GCATCTGTCTTGAAA[A/C]TTTTTTCTTTTAAAT | 51136 |
rs561074369 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955036 | CTGCTTTCTGTAGAA[A/C]TGATGGGGAAGAGGT | 51136 |
rs561563578 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954881 | TATTTGAATTTTCTT[C/T]TCTTCTAATGTCCTA | 51136 |
rs561995422 | snp | G/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963126 | CCAGAATGAGGGCAA[G/T]AACCCTCTCCTGTCA | 51136 |
rs562336620 | in-del | -/C | 0.00676609 | 0.0577691 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956046 | CCAGTAAGAAAACTG[-/C]CAAGAGACATGATTT | 51136 |
rs562852645 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962373 | CAGCATTAGGAGAGA[G/T]AATTTATTCCAGGAT | 51136 |
rs563026416 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59951970 | GAGCTTCAATCTTCC[A/G]ATTGATGGTGATTCA | 51136 |
rs563223522 | snp | C/G | 0.000682111 | 0.0184551 | missense | RNFT1 | GRCh38.p7 | 17:59960135 | CTGCTAAGAATACCA[C/G]TAACCAAGCACACTG | 51136 |
rs563617775 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956400 | TCATCTATTTATGAA[A/T]TCCATTCTTGTAAAA | 51136 |
rs563680388 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955739 | CTTTTTTTATTTTTA[C/T]GGTATATTATTCGGT | 51136 |
rs563741713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964285 | GTCACCGTGTCTGGC[A/G]GTTTGGGTTTCAGTG | 51136 |
rs564000714 | snp | C/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966670 | TGTAGTGTTTAAATT[C/G]TCATCTTGGCCAGAT | 51136 |
rs564335135 | snp | A/T | 1.65924e-05 | 0.00288027 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963241 | GCATGGCCCTTAAAT[A/T]CTTTTTCTCTGACCC | 51136 |
rs564391983 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955694 | AAAAGGCCCTGGCCA[A/G]TTAGTCTCGTTTACT | 51136 |
rs564524814 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963965 | CACGTAATTGCTAGG[-/T]TAACTCTTTAGTCTG | 51136 |
rs564905349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959522 | GTACTTTAAAAATAC[A/G]AAATATGTAAACAAA | 51136 |
rs565221380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958001 | ATAGTCAACTGTCAA[C/T]TGATAATGCCCTGGA | 51136 |
rs565302790 | in-del | -/A | 0.000736761 | 0.0191791 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962648 | CCAGTTAATTGAAAG[-/A]AAAAAAAAATCAAAG | 51136 |
rs565455506 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954547 | TCAATCCAGCCAGAG[A/G/T]TTGGCTGGTTGAATG | 51136 |
rs565601531 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965948 | GTGAGCCGGGATTAG[C/T]CACTGCACTCCAGCC | 51136 |
rs566143734 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964448 | TGCACAGACAAGAAA[A/G]AGGAGAAAAAAGGGA | 51136 |
rs566326342 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963669 | CTCTGATGTAGATTC[C/T]ACATCAAAGAAGTTT | 51136 |
rs566629499 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959743 | GGTGAAACTCCGTCT[C/G]TATTAAAAATACAAA | 51136 |
rs566669888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960504 | AAGCCAGGTCTTCTA[C/T]AAGCTGACATAAAGG | 51136 |
rs567410171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959703 | GAGGCAGGCAGATCA[C/T]GAGGTCAGGAGGTCT | 51136 |
rs567661868 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956751 | GCTGAAGTACATTTA[A/C]ACACCTAGAGTAACA | 51136 |
rs567865858 | snp | A/G | 0.000209762 | 0.010239 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964709 | TCAACCGCAAACCCC[A/G]CAAGCTCTTCTCTCA | 51136 |
rs568052888 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953369 | CCATGCCCAGCTAGT[G/T]TTTTTATTTTTAGTA | 51136 |
rs569028185 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952587 | TTCTACTTTTAGATA[A/G]TATGTATCTTAAAAT | 51136 |
rs569042078 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953256 | GCCGGAGTGCAATGG[C/T]ACCATCTCGGCTCAC | 51136 |
rs569105517 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955971 | GAGACTCAATTAATT[A/G]TTAAATTTCATGCCA | 51136 |
rs569315765 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964940 | GTTGTTATGTGTTAT[A/G]TATTTATGTGGCATC | 51136 |
rs569378779 | snp | C/T | 0.000392465 | 0.0140028 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964573 | GCCGCGGCCCCTCGC[C/T]GCCTCCTCCTCTGCC | 51136 |
rs569784559 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956134 | AGGAGTTAATAGGAA[A/C]AAACAAAGCCCCCAT | 51136 |
rs570135052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955151 | CTTGTACTAAAACGT[C/T]TCAGGCTAACAACAT | 51136 |
rs570268303 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962674 | CAAAGAGGATTATAT[A/C]AGCTAACAATGACAC | 51136 |
rs570704497 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955053 | GATGGGGAAGAGGTA[A/T]CTAAAGAGATGTAAG | 51136 |
rs570836715 | snp | A/C | 0.000142656 | 0.00844438 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954183 | TTCATCTACAAATTT[A/C]TTTCTTTCCTGTTCC | 51136 |
rs571057213 | in-del | -/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952722 | AAAACACATTTACAA[-/T]TTTAACACTGCAGTT | 51136 |
rs571226737 | snp | A/G | 0.000316738 | 0.0125805 | missense | RNFT1 | GRCh38.p7 | 17:59958388 | TCTGTAATTCCAACA[A/G]TCCAAAATACTTCCC | 51136 |
rs571461164 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966161 | GCTTGGTGGCGGGCG[C/T]CTGTAATCCCAGCTA | 51136 |
rs571640984 | snp | A/C | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964512 | AGGGCAGAGTTCTCC[A/C]CCCACGTCCGAGCCT | 51136 |
rs571758764 | snp | C/T | 0.000210715 | 0.0102622 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956600 | TTCAAACAGTCCTAT[C/T]TGCTAAACCCAAAAA | 51136 |
rs571929480 | snp | A/C | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952758 | TCAAATAATTAGAAT[A/C]GAATAAATGTTGCAT | 51136 |
rs572146185 | snp | C/T | 0.000197713 | 0.0099407 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964685 | CCTCCAGCCCTTCAG[C/T]CGGGGCCATCAACCG | 51136 |
rs572148763 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954535 | TGGTTCATAAAGTCA[A/G]TCCAGCCAGAGGTTG | 51136 |
rs572267068 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964124 | CTCCTAGAAACAGAA[A/G]AACAGAGTCGGAATC | 51136 |
rs572766791 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964102 | TAATAAATGATCCAG[C/T]GTGGACCTCCTAGAA | 51136 |
rs573153225 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957912 | TGCAAGTAAAACCTA[C/T]GTGAGTATGTTTTTG | 51136 |
rs573217308 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966637 | CATTTGGTACATTTG[C/T]AAATTTAGAATACCA | 51136 |
rs573309763 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965639 | GGTCTCAAAAAATAA[A/C]TAAATAAAATAAATT | 51136 |
rs573905842 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966456 | TATAGTGAATTTTCC[A/G]AGGAGATATGTGTAA | 51136 |
rs573946838 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957860 | AAAACAAAACAAAAC[A/C]AAAAAAAAAGATACA | 51136 |
rs574170612 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957894 | AGAATGTTTTATGTA[C/T]ACTGCAAGTAAAACC | 51136 |
rs574373267 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962150 | TCGGCCTCCCAAAGT[G/T]CTGGGATTACAGGTG | 51136 |
rs575215116 | snp | A/G | | | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962355 | AGGTAAGGTGAAGGA[A/G]TTCAGCATTAGGAGA | 51136 |
rs575229033 | snp | C/G | 0 | 0 | intron-variant | RNFT1 | GRCh38.p7 | 17:59959852 | GAGGCAAAGGTTGCA[C/G]TGAGCCAAGATCAAG | 51136 |
rs575405855 | snp | A/G | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952276 | TTTAATAGTTACTTC[A/G]AGATACTCCATGGTA | 51136 |
rs575424934 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966715 | CTATAATCCTAGCAC[A/T]TTGGGAGGCTGAGGT | 51136 |
rs576071446 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961100 | GGAGTGCAGTGGCAT[G/T]ATCACAACTCACTGC | 51136 |
rs576135280 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957677 | TGGTGAAACCCCGTC[C/T]CTACTAAAAATACAA | 51136 |
rs576479781 | snp | A/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963400 | AATCACAACAGATGA[A/T]TTTTCAGGTTATTTA | 51136 |
rs576583067 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953794 | CCAATTATAAAATAG[C/T]CTGTTTTTTAATCAC | 51136 |
rs576628440 | snp | A/G | 1.65839e-05 | 0.00287953 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59953028 | CTTCCATTTGTTTAT[A/G]TGGTCTGAAATCACA | 51136 |
rs576778463 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59961973 | TCACTGCAACCTCCA[C/T]CTCCCAGGTTCAAGT | 51136 |
rs576836875 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961278 | CCTGGGCTCAAGCAA[C/T]CTGCCCATCTCAGCC | 51136 |
rs576883818 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962264 | GGACTTGCCAAATCA[C/G]ATCAGATACCGTGTT | 51136 |
rs577278421 | snp | C/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965865 | GTGTGGTGGTGCGTG[C/T]CTGTAATCTCAGCTA | 51136 |
rs577303452 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952750 | GTTACCTGTCAAATA[A/G]TTAGAATAGAATAAA | 51136 |
rs577360930 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59951941 | ATCAAAACCTCATGA[C/T]CACCTCTCAGTGCGA | 51136 |
rs577366593 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNFT1 | GRCh38.p7 | 17:59961204 | ACCACGCCCAGCTAA[G/T]TTTTTGTATTTTTTG | 51136 |
rs577756482 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956918 | GATACTCTACTAGTT[G/T]AAGAATTATGTGTAT | 51136 |
rs577826357 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956363 | CAAAGTACTAGAAAA[C/T]AATCAAAGTAAAAGA | 51136 |
rs578210942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNFT1 | GRCh38.p7 | 17:59955460 | TATCCTCTCTGTAGT[C/T]TGTCTCAGAGAAAGA | 51136 |
rs745362088 | snp | A/C | 1.66693e-05 | 0.00288693 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962598 | AAAGTTGTTAGCAGC[A/C]CAATTCCAAGAGAAA | 51136 |
rs745450937 | snp | C/T | 1.65897e-05 | 0.00288003 | missense | RNFT1 | GRCh38.p7 | 17:59953008 | TGTGATGAAGTGGCT[C/T]CATCCTTCCATTTGT | 51136 |
rs745534037 | snp | A/G | 1.73021e-05 | 0.00294121 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953157 | TTTGATAATCATTTT[A/G]AATCCATCACATTGT | 51136 |
rs745840803 | snp | C/T | 1.66475e-05 | 0.00288504 | missense | RNFT1 | GRCh38.p7 | 17:59960167 | ATCTTTGAGGACCTT[C/T]CCTGAAAGATAAACA | 51136 |
rs745857388 | in-del | -/A | 1.66461e-05 | 0.00288492 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59957343 | GAACAAAAGTTCGGT[-/A]GTATTGACACAATTC | 51136 |
rs745916710 | snp | A/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963019 | TGTGTACACATCCAT[A/G]GGCACAGCTATGGAC | 51136 |
rs746007285 | snp | A/G | 1.64727e-05 | 0.00286986 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963142 | AACCCTCTCCTGTCA[A/G]TCTTGTGTGGACACA | 51136 |
rs746181396 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958823 | ATCAACTCCCTCTGT[A/G]TGGCTAAATTTCAAG | 51136 |
rs746249689 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960881 | TGACTCACTTGTCAA[G/T]GTTTATATTTTTTAA | 51136 |
rs746301020 | snp | C/G | 1.71784e-05 | 0.00293069 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958475 | CATCAAAATTTATCA[C/G]AGCAACATACAAAGA | 51136 |
rs746445828 | snp | C/G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954299 | AAGCTGAGCCATATA[C/G/T]AGAACCACCTCTTGA | 51136 |
rs746477440 | snp | C/G | 3.31356e-05 | 0.00407022 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954001 | CTTTTGCAAGTCACA[C/G]AGAACTGTTGTATTT | 51136 |
rs746525236 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958577 | AGGATGTCAGAGTTC[A/C]CAATAATGGAATGGA | 51136 |
rs746559069 | snp | A/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955218 | AAAATTGAGGTTTTT[A/T]GAAACTGGTAATAAA | 51136 |
rs746618504 | snp | A/G | 3.37285e-05 | 0.00410647 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964689 | CAGCCCTTCAGTCGG[A/G]GCCATCAACCGCAAA | 51136 |
rs746789047 | in-del | -/T | 1.65864e-05 | 0.00287974 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958283 | TAAAGCATAAGTGAG[-/T]TTCTTACCTTAGATT | 51136 |
rs746802423 | in-del | -/AA | 6.93758e-05 | 0.00588923 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962660 | AAAGAAAAAAAAATC[-/AA]AGAGGATTATATAAG | 51136 |
rs746836194 | snp | A/G | 1.69755e-05 | 0.00291332 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962637 | AGAAAATAAGTTCCA[A/G]TTAATTGAAAGAAAA | 51136 |
rs746840664 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965413 | CACTTGAGCTCAGGA[A/G]GTAGAGACCAGCCTG | 51136 |
rs747068326 | snp | C/T | 3.55423e-05 | 0.00421543 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963307 | ATCAAATAAAAGATA[C/T]TCTAAGTAAACAGGC | 51136 |
rs747068367 | snp | A/C | 1.68482e-05 | 0.00290238 | missense | RNFT1 | GRCh38.p7 | 17:59956500 | TACTGGTTGTGTAAA[A/C]AATATTCGTAAAACC | 51136 |
rs747156391 | snp | A/T | 1.681e-05 | 0.00289909 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957212 | AGTGACAAGATTTGT[A/T]ATGTTACCTACTTTT | 51136 |
rs747200071 | in-del | -/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954878 | AATTATTTGAATTTT[-/C]TTCTCTTCTAATGTC | 51136 |
rs747344879 | snp | A/C | 1.66421e-05 | 0.00288458 | missense | RNFT1 | GRCh38.p7 | 17:59960134 | CCTGCTAAGAATACC[A/C]GTAACCAAGCACACT | 51136 |
rs747502332 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961005 | AAGCATTCTTCCCAA[A/C]TCAGCCTCCCAAGTA | 51136 |
rs747544806 | snp | C/G | 8.23635e-05 | 0.00641677 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963162 | GTGTGGACACACTGA[C/G]GGGTTGAGGCATCCT | 51136 |
rs747790693 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955348 | GACAAGCTTTTAAGA[C/T]GTTACTCATCTGGCA | 51136 |
rs747803991 | in-del | -/TCT | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961583 | GGGTTTCATTTTCTC[-/TCT]TTTTTTTTTTGAGAT | 51136 |
rs747850231 | in-del | -/TAAA | 0.000314874 | 0.0125434 | frameshift-variant, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963236 | GGCTTGCATGGCCCT[-/TAAA]TACTTTTTCTCTGAC | 51136 |
rs747899300 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966491 | TCTAACATTTCAACT[A/G]TGTCGTGGATATTTT | 51136 |
rs747925686 | snp | C/T | 1.65149e-05 | 0.00287353 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962882 | AATATATGGAAGACT[C/T]TTTTGCAGCCACTTG | 51136 |
rs748065205 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963593 | CCAGCAGATGTTAAT[A/G]AGCACCAGTCCTCAC | 51136 |
rs748202547 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961165 | CCTCAGCCTCCCAGA[G/T]AGCAGAGATTACAGG | 51136 |
rs748211939 | snp | A/C | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963099 | ATGGAGTTTATCTGG[A/C]TATGAACATCTCCAG | 51136 |
rs748499116 | snp | A/C | 1.66308e-05 | 0.00288359 | missense | RNFT1 | GRCh38.p7 | 17:59952982 | TTTATACAACTTAAT[A/C]TATTTGAAGGTGTGA | 51136 |
rs748601137 | snp | C/T | 6.43687e-05 | 0.00567276 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964575 | CGCGGCCCCTCGCCG[C/T]CTCCTCCTCTGCCCG | 51136 |
rs748606179 | snp | C/T | 6.09942e-05 | 0.00552208 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964668 | AACAGCGGCATACAC[C/T]GCCTCCAGCCCTTCA | 51136 |
rs748771377 | snp | A/G | 3.39472e-05 | 0.00411976 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960021 | AAAGTGCTATGAAAT[A/G]TATGATTACATTAAA | 51136 |
rs748857449 | snp | A/T | 1.66407e-05 | 0.00288446 | missense | RNFT1 | GRCh38.p7 | 17:59960141 | AGAATACCAGTAACC[A/T]AGCACACTGAATCTT | 51136 |
rs748931984 | snp | C/T | | | missense | RNFT1 | GRCh38.p7 | 17:59958430 | TGGTCCAAAGTAGGA[C/T]TTAAAAAAATTAAGC | 51136 |
rs748972321 | snp | C/T | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952416 | CTACAGAGAATAATA[C/T]AATACTATAATGTAT | 51136 |
rs749019062 | snp | A/T | 3.29451e-05 | 0.00405851 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963132 | TGAGGGCAAGAACCC[A/T]CTCCTGTCAATCTTG | 51136 |
rs749073094 | snp | C/G | 1.71252e-05 | 0.00292614 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954154 | CCATAACTCTATGAA[C/G]ATAGTAAGTTCTGTT | 51136 |
rs749112766 | snp | A/C | | | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963088 | ATTCTTTAGGTATGG[A/C]GTTTATCTGGATATG | 51136 |
rs749165739 | snp | C/G | 1.74974e-05 | 0.00295776 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956470 | AGGTGTTTTTCTTAA[C/G]TGATAAAAAGTACTT | 51136 |
rs749320725 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965314 | GTTCTAAAATTAAAA[A/G]GTTATTAAGAAAACG | 51136 |
rs749416565 | snp | C/T | 1.64787e-05 | 0.00287038 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962907 | CACTTGAAGAGATAG[C/T]GGAATTCTGAGAAGG | 51136 |
rs749518496 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963459 | GCCAAGGCTCTGCTG[C/T]CCTACACAAATGATC | 51136 |
rs749559183 | snp | A/G | 3.29457e-05 | 0.00405854 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963005 | ACCCCGTAAGCGACT[A/G]TGTACACATCCATGG | 51136 |
rs749640882 | snp | C/T | 6.35647e-05 | 0.00563723 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964679 | ACACCGCCTCCAGCC[C/T]TTCAGTCGGGGCCAT | 51136 |
rs749723913 | snp | A/G | 3.61096e-05 | 0.00424894 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957395 | ACCCTAAAAAATAAG[A/G]AGAAAACAAATAGAG | 51136 |
rs749764352 | snp | A/G | 1.66446e-05 | 0.00288479 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59958369 | AAAGAATTTCAGAAT[A/G]AAGTCTGTAATTCCA | 51136 |
rs749901157 | in-del | -/T | | | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962320 | TTTAACAGTAACCAA[-/T]TTTTTTTTTCTTACA | 51136 |
rs749969685 | snp | A/G | 1.66624e-05 | 0.00288633 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962844 | GTTATATGCTGCATA[A/G]CAAGTTTGACGCTCA | 51136 |
rs750101638 | snp | A/G | 3.29462e-05 | 0.00405857 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962951 | ATCTCCAGATTCTGC[A/G]GCAGTATCATCAGTC | 51136 |
rs750110481 | snp | C/G | | | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964635 | GAAGCGGACGGAGGT[C/G]TCGGGAGCGACAGCA | 51136 |
rs750167733 | snp | A/C | 2.85759e-05 | 0.00377983 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964641 | GACGGAGGTGTCGGG[A/C]GCGACAGCAAGAACA | 51136 |
rs750577321 | snp | A/G | 1.69069e-05 | 0.00290743 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952927 | GCCTTATCAGTAGTC[A/G]TTATGACCAAATGAC | 51136 |
rs750651147 | snp | C/T | 1.68635e-05 | 0.0029037 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963271 | CAGATGTCTTTGCTT[C/T]AGGCCTCTGTCTCCT | 51136 |
rs750930803 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953478 | AGTTCTGGGATTACA[G/T]GCGTGAGCCACTGTG | 51136 |
rs750980793 | snp | G/T | 1.66657e-05 | 0.00288662 | missense | RNFT1 | GRCh38.p7 | 17:59960116 | TATAAAAGAACAGAA[G/T]ATCCTGCTAAGAATA | 51136 |
rs751116466 | snp | C/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963097 | GTATGGAGTTTATCT[C/G]GATATGAACATCTCC | 51136 |
rs751208395 | snp | G/T | 1.80762e-05 | 0.00300629 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956451 | TTGCAGTGAAGAAAG[G/T]TGAAGGTGTTTTTCT | 51136 |
rs751312343 | snp | C/T | 1.65836e-05 | 0.0028795 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958286 | AGCATAAGTGAGTTT[C/T]TTACCTTAGATTTAA | 51136 |
rs751581110 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957890 | AATGAGAATGTTTTA[G/T]GTATACTGCAAGTAA | 51136 |
rs751621827 | snp | A/G | 1.66175e-05 | 0.00288244 | missense | RNFT1 | GRCh38.p7 | 17:59953083 | TCTCTGTTAAACCAT[A/G]AGGTCATGCACTCTT | 51136 |
rs751676859 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954646 | CAGACATATTGGGAT[A/G]TGACCCAGTAATCTA | 51136 |
rs751742896 | snp | A/C | 3.88901e-05 | 0.00440948 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964703 | GGGCCATCAACCGCA[A/C]ACCCCGCAAGCTCTT | 51136 |
rs751790687 | snp | C/G | 1.67449e-05 | 0.00289347 | missense | RNFT1 | GRCh38.p7 | 17:59957353 | TCGGTAGTATTGACA[C/G]AATTCTTCTAAAAGC | 51136 |
rs751944208 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964840 | CGCCGAGTGGAGAGC[C/T]CACGGCTGCCGGGGT | 51136 |
rs751992695 | snp | A/G | 1.68272e-05 | 0.00290057 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952949 | CCAAATGACATTAGT[A/G]TTTTGTGGCCTTGAT | 51136 |
rs752046834 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961616 | GGAGTCTCACTCTGT[C/T]GCCAGGCTGGAGTGC | 51136 |
rs752123845 | snp | A/G | 3.37109e-05 | 0.0041054 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962829 | TATTATGTCCTACCT[A/G]TTATATGCTGCATAA | 51136 |
rs752176193 | in-del | -/CATAACTCTATGAAG | 1.67522e-05 | 0.0028941 | cds-indel | RNFT1 | GRCh38.p7 | 17:59954123 | TCTGAACACTGTCTC[-/CATAACTCTATGAAG]TTGCTGGCAGCCACT | 51136 |
rs752208915 | snp | C/T | 1.65034e-05 | 0.00287253 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963216 | CTGTGCAGTTGGCTA[C/T]GATTGGCTTGCATGG | 51136 |
rs752209004 | snp | A/G | 1.78506e-05 | 0.00298747 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956459 | AAGAAAGGTGAAGGT[A/G]TTTTTCTTAACTGAT | 51136 |
rs752693194 | snp | A/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963121 | CATCTCCAGAATGAG[A/G]GCAAGAACCCTCTCC | 51136 |
rs752800880 | snp | A/G | 1.67125e-05 | 0.00289067 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964712 | ACCGCAAACCCCGCA[A/G]GCTCTTCTCTCAGCC | 51136 |
rs752837024 | snp | A/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954872 | AAATGCAATTATTTG[A/T]ATTTTCTTCTCTTCT | 51136 |
rs752890788 | snp | C/T | 1.66145e-05 | 0.00288218 | missense | RNFT1 | GRCh38.p7 | 17:59958346 | ATAAGGCATTTTAAG[C/T]CCATGAAAAAGAATT | 51136 |
rs752897238 | in-del | -/AAACTT | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959150 | TCTACTTAGCCTCTC[-/AAACTT]AACATGTTCAAAACA | 51136 |
rs752980878 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956001 | ATGAACGTATTTATG[C/T]ACATATAATTGAGCA | 51136 |
rs753015687 | snp | C/T | 1.67601e-05 | 0.00289478 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962835 | GTCCTACCTGTTATA[C/T]GCTGCATAACAAGTT | 51136 |
rs753025205 | in-del | -/TC | 1.79822e-05 | 0.00299846 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954186 | ATCTACAAATTTCTT[-/TC]TTTCCTGTTCCTCAA | 51136 |
rs753045601 | snp | C/T | 1.6671e-05 | 0.00288708 | missense | RNFT1 | GRCh38.p7 | 17:59953101 | GTCATGCACTCTTCA[C/T]AAAATATATGCTGTA | 51136 |
rs753048140 | in-del | -/CC | 1.66475e-05 | 0.00288504 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59960167 | TCTTTGAGGACCTTT[-/CC]CCTGAAAGATAAACA | 51136 |
rs753227980 | snp | A/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965224 | GTGGAAGTAGAAGTT[A/T]GAGTTGAAAAACCTG | 51136 |
rs753236208 | snp | C/T | 5.02256e-05 | 0.00501102 | missense | RNFT1 | GRCh38.p7 | 17:59954062 | GACAAATGAGAAGAA[C/T]TGGCTTCTGAAATTC | 51136 |
rs753249754 | snp | A/G | 1.65734e-05 | 0.00287862 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59957278 | ACTCCATCTAGTTAC[A/G]TTACCAAACTCCCCA | 51136 |
rs753318019 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960627 | ACCAGCCTGCCCAAC[A/G]TGGTGAAACCTGTCT | 51136 |
rs753539166 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966190 | TACTCGGGAGGCTGA[A/G]GCAGGAGAATCCCTT | 51136 |
rs753735830 | snp | A/G | 3.19453e-05 | 0.00399645 | synonymous-codon, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964619 | TAACCTCTCATGACC[A/G]GAAGCGGACGGAGGT | 51136 |
rs753841235 | snp | C/G | 1.70249e-05 | 0.00291756 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956570 | TGAAAAGAGAAATAA[C/G]AGATCATTTATTAAT | 51136 |
rs753999311 | snp | A/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966684 | TCTCATCTTGGCCAG[A/T]TACTACGGTTCATTC | 51136 |
rs754161388 | snp | A/T | 1.66852e-05 | 0.0028883 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59954087 | AAATTCAGCTTGACA[A/T]ATTGAACAAATATCA | 51136 |
rs754574562 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956262 | AAATATATAAGCACT[C/G]CAACAATTAGCAGGT | 51136 |
rs754877636 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957896 | AATGTTTTATGTATA[C/T]TGCAAGTAAAACCTA | 51136 |
rs754999301 | snp | C/T | 8.9295e-05 | 0.00668128 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964663 | GCAAGAACAGCGGCA[C/T]ACACCGCCTCCAGCC | 51136 |
rs755211761 | snp | G/T | 1.65864e-05 | 0.00287974 | missense | RNFT1 | GRCh38.p7 | 17:59958295 | GAGTTTCTTACCTTA[G/T]ATTTAAAAGGCATGA | 51136 |
rs755235767 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953854 | TTTTTCCCCTTCATA[A/C]GCTCCTCTGCATAAA | 51136 |
rs755299506 | snp | C/G | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965164 | AGGATCAGGCCTTGT[C/G]AGAACCCGAGATGAG | 51136 |
rs755360113 | snp | C/T | 1.66349e-05 | 0.00288395 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962565 | ACCTGATTTACAATG[C/T]TTTTGTTTGCATACA | 51136 |
rs755361749 | in-del | -/CT | 5.08298e-05 | 0.00504106 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59954145 | GCAGCCACTCCATAA[-/CT]CTATGAAGATAGTAA | 51136 |
rs755450258 | snp | C/T | 1.67562e-05 | 0.00289444 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952960 | TAGTATTTTGTGGCC[C/T]TGATAGTTTATACAA | 51136 |
rs755465759 | snp | G/T | 1.66228e-05 | 0.0028829 | missense | RNFT1 | GRCh38.p7 | 17:59953086 | CTGTTAAACCATAAG[G/T]TCATGCACTCTTCAC | 51136 |
rs755647969 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958090 | TTATTCTGAAGCAAA[C/T]ATAATTCTGATTTTA | 51136 |
rs755689560 | in-del | -/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955025 | ACAAATGAAACCTGC[-/T]TTCTGTAGAAATGAT | 51136 |
rs755740095 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960356 | CAAACAGAACTCTTA[C/T]ATTAAACAAATGTTT | 51136 |
rs755924116 | snp | C/G | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952144 | GCAGTCCTCCTGCCT[C/G]TGCCTCCCAAAGTGC | 51136 |
rs755957295 | snp | C/T | 0.000115305 | 0.00759205 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963000 | GAGTGACCCCGTAAG[C/T]GACTGTGTACACATC | 51136 |
rs756082554 | snp | G/T | 1.64727e-05 | 0.00286986 | stop-gained, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963122 | ATCTCCAGAATGAGG[G/T]CAAGAACCCTCTCCT | 51136 |
rs756174542 | snp | G/T | 1.78232e-05 | 0.00298518 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956460 | AGAAAGGTGAAGGTG[G/T]TTTTCTTAACTGATA | 51136 |
rs756296066 | snp | A/G | 1.68046e-05 | 0.00289862 | missense | RNFT1 | GRCh38.p7 | 17:59958428 | AATGGTCCAAAGTAG[A/G]ATTTAAAAAAATTAA | 51136 |
rs756318571 | in-del | -/GT | 5.4307e-05 | 0.00521062 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956451 | TTGCAGTGAAGAAAG[-/GT]GAAGGTGTTTTTCTT | 51136 |
rs756596570 | snp | C/G/T | 6.18071e-05 | 0.00555882 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964673 | CGGCATACACCGCCT[C/G/T]CAGCCCTTCAGTCGG | 51136 |
rs756655934 | snp | C/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966650 | TGTAAATTTAGAATA[C/G]CAAATGTAGTGTTTA | 51136 |
rs756697513 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958992 | CCAGTACTGGGCTCT[C/T]TATCTACACTCTCTT | 51136 |
rs756866664 | snp | C/T | 1.66463e-05 | 0.00288494 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962588 | TGCATACATAAAAGT[C/T]GTTAGCAGCCCAATT | 51136 |
rs756870232 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960659 | TACTAAAAAAAGTAC[A/G]AAAGTTAGCCAGGCG | 51136 |
rs756952609 | snp | A/G | 1.67086e-05 | 0.00289033 | stop-gained, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962839 | TACCTGTTATATGCT[A/G]CATAACAAGTTTGAC | 51136 |
rs756990650 | snp | C/T | 1.66765e-05 | 0.00288756 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963256 | ACTTTTTCTCTGACC[C/T]AGATGTCTTTGCTTC | 51136 |
rs757063709 | snp | A/G | 6.96888e-05 | 0.00590251 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956472 | GTGTTTTTCTTAACT[A/G]ATAAAAAGTACTTAC | 51136 |
rs757097754 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954898 | CTTCTAATGTCCTAA[C/T]AACAAGTTACTCGTC | 51136 |
rs757241960 | snp | A/G | 1.65784e-05 | 0.00287905 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59957302 | CTCCCCATAGCTTAT[A/G]AGGTAGCGAAACCAA | 51136 |
rs757308195 | in-del | -/GC | 1.68545e-05 | 0.00290292 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962525 | AATAATTTTTTAGTT[-/GC]TTGTTATACTTACTC | 51136 |
rs757406435 | snp | A/G | 1.67399e-05 | 0.00289304 | missense | RNFT1 | GRCh38.p7 | 17:59960102 | AATGAAAGGTGTAAT[A/G]TAAAAGAACAGAAGA | 51136 |
rs757540470 | snp | C/G | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963135 | GGGCAAGAACCCTCT[C/G]CTGTCAATCTTGTGT | 51136 |
rs757704330 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958682 | TCTTCACGGTTTGTC[A/C]TAGTTGACACCTTTC | 51136 |
rs757889420 | snp | A/C | 3.41927e-05 | 0.00413463 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958463 | CCAAAAGAAAAACAT[A/C]AAAATTTATCAGAGC | 51136 |
rs757920434 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962971 | TATCATCAGTCAGCC[C/T]TGCTTCACTGTGGGA | 51136 |
rs757941995 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955683 | CTATCTTAGGGAAAA[A/G]GCCCTGGCCAGTTAG | 51136 |
rs757980471 | snp | A/C | 2.40076e-05 | 0.00346457 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953997 | TTGACTTTTGCAAGT[A/C]ACAGAGAACTGTTGT | 51136 |
rs758068692 | snp | C/T | 3.33706e-05 | 0.00408463 | missense | RNFT1 | GRCh38.p7 | 17:59954089 | ATTCAGCTTGACATA[C/T]TGAACAAATATCATC | 51136 |
rs758087851 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956167 | GTGGATTAAAAAAGA[C/G]GAACACAATTTCATA | 51136 |
rs758122913 | snp | C/T | 0.000149697 | 0.0086502 | missense | RNFT1 | GRCh38.p7 | 17:59957339 | ATGGGAACAAAAGTT[C/T]GGTAGTATTGACACA | 51136 |
rs758268867 | in-del | -/A | 0.000736761 | 0.0191791 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962649 | CCAGTTAATTGAAAG[-/A]AAAAAAAATCAAAGA | 51136 |
rs758462778 | in-del | -/TAGA | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952580 | ACAAAATTCTACTTT[-/TAGA]TAGATAGTATGTATC | 51136 |
rs758600191 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953541 | TCCCCTCATTTTACA[A/G]TTGTGAAAATGGAGA | 51136 |
rs758664977 | snp | C/G | 2.84831e-05 | 0.00377369 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964642 | ACGGAGGTGTCGGGA[C/G]CGACAGCAAGAACAG | 51136 |
rs758730157 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960963 | AATATATGGGGTCTC[G/T]ACACATTGCTCAGAA | 51136 |
rs758819984 | snp | A/G | | | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962772 | ATTACCAATAATGAA[A/G]GAAAATTAACTGAAT | 51136 |
rs758820786 | snp | A/G | 1.71953e-05 | 0.00293212 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958476 | ATCAAAATTTATCAG[A/G]GCAACATACAAAGAT | 51136 |
rs758927451 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958052 | ATAGTTTCCCACATA[C/T]GATGTGGGGACTGAT | 51136 |
rs758929184 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954550 | ATCCAGCCAGAGGTT[-/G]GCTGGTTGAATGTAA | 51136 |
rs759208191 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953618 | CCACTAGTGTTCTGG[C/T]TGTACCATCCATTTA | 51136 |
rs759260685 | snp | A/G | 1.67837e-05 | 0.00289682 | missense | RNFT1 | GRCh38.p7 | 17:59956535 | TGAAAGTTCTCAGAT[A/G]CCCAAAAAATTCCAA | 51136 |
rs759286951 | snp | C/T | 9.57167e-05 | 0.00691731 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964596 | CCTCTGCCCGCTTCC[C/T]CCAGGCCTAACCTCT | 51136 |
rs759325052 | snp | A/G | 5.02163e-05 | 0.00501055 | missense | RNFT1 | GRCh38.p7 | 17:59958416 | CCCAGAAGCTCAAAT[A/G]GTCCAAAGTAGGATT | 51136 |
rs759415109 | snp | C/T | 1.69329e-05 | 0.00290967 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960058 | ATTGTGTATTTGGAC[C/T]TCTAATTACCTGTAA | 51136 |
rs759616510 | in-del | -/GATCTCTCTAATAAAT | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964079 | ACTCTAGCAGAGAAA[-/GATCTCTCTAATAAAT]GATCCAGTGTGGACC | 51136 |
rs759651735 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960673 | CAAAAGTTAGCCAGG[C/G]GCCGTGGCACGTGCC | 51136 |
rs759708315 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955969 | CAGAGACTCAATTAA[C/T]TGTTAAATTTCATGC | 51136 |
rs759952186 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956998 | TACTTAGATAATCCA[C/T]GCTATGTGAAGGTCG | 51136 |
rs760070387 | in-del | -/T | 1.67632e-05 | 0.00289505 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59960101 | GAATGAAAGGTGTAA[-/T]ATAAAAGAACAGAAG | 51136 |
rs760103344 | snp | A/C | 1.66051e-05 | 0.00288137 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964617 | CCTAACCTCTCATGA[A/C]CAGAAGCGGACGGAG | 51136 |
rs760331059 | in-del | -/CA | 2.393e-05 | 0.00345897 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953997 | TTGACTTTTGCAAGT[-/CA]CAGAGAACTGTTGTA | 51136 |
rs760347973 | snp | A/G | 1.6574e-05 | 0.00287867 | missense | RNFT1 | GRCh38.p7 | 17:59957273 | CCAAGACTCCATCTA[A/G]TTACGTTACCAAACT | 51136 |
rs760490467 | snp | G/T | 1.704e-05 | 0.00291885 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962517 | AAACAGTTAATAATT[G/T]TTTAGTTGCTTGTTA | 51136 |
rs760493364 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963671 | CTGATGTAGATTCTA[A/C]ATCAAAGAAGTTTCA | 51136 |
rs760696537 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957674 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 51136 |
rs760829966 | snp | A/G/T | 3.3582e-05 | 0.00409757 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59960094 | TGACTGAGAATGAAA[A/G/T]GTGTAATATAAAAGA | 51136 |
rs760883709 | in-del | -/AT | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952252 | CTGTTTATAATCCAC[-/AT]GAATTATTTTAATAG | 51136 |
rs761004007 | in-del | -/GAGA | 5.39962e-05 | 0.00519569 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962497 | TCTCTAAAATCTATG[-/GAGA]GAAACAGTTAATAAT | 51136 |
rs761113495 | snp | C/T | 3.33823e-05 | 0.00408534 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59954081 | CTTCTGAAATTCAGC[C/T]TGACATATTGAACAA | 51136 |
rs761115438 | snp | G/T | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963050 | ACCTGACCTTATATT[G/T]CTGGAGCTTGCATTT | 51136 |
rs761196281 | snp | A/G | 1.65932e-05 | 0.00288034 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958252 | GCATTAATGTGATTC[A/G]ATAACATCACTCCAA | 51136 |
rs761203327 | snp | A/G | 1.7436e-05 | 0.00295258 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954167 | AAGATAGTAAGTTCT[A/G]TTCATCTACAAATTT | 51136 |
rs761239226 | in-del | -/ATC | 0.000166814 | 0.00913122 | cds-indel | RNFT1 | GRCh38.p7 | 17:59954099 | ACATATTGAACAAAT[-/ATC]ATCCACATCTGAACA | 51136 |
rs761276175 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964424 | ATAGAACCCTCCCAC[C/T]TTCCTTCATGCACAG | 51136 |
rs761345217 | snp | C/T | | | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962032 | CTGGGAATACAGGCA[C/T]ATGCCACCACACCTA | 51136 |
rs761379781 | in-del | -/AAAGAT | 1.73586e-05 | 0.00294601 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958486 | ATCAGAGCAACATAC[-/AAAGAT]AAAGTATTAATAAAG | 51136 |
rs761445008 | snp | A/G | 0.000116683 | 0.00763728 | missense | RNFT1 | GRCh38.p7 | 17:59958385 | AAGTCTGTAATTCCA[A/G]CAATCCAAAATACTT | 51136 |
rs761745837 | snp | A/C | 0.000149905 | 0.00865621 | synonymous-codon, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964628 | ATGACCAGAAGCGGA[A/C]GGAGGTGTCGGGAGC | 51136 |
rs761804872 | snp | A/C | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965735 | GTAGCTCACACCTGT[A/C]ATCCCAGCACTTTGG | 51136 |
rs762032546 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953363 | CCACCACCATGCCCA[A/G]CTAGTTTTTTTATTT | 51136 |
rs762048699 | snp | A/G | 0.00159714 | 0.0282138 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963198 | CTTCCAGTTCCTGGA[A/G]GACTGTGCAGTTGGC | 51136 |
rs762067640 | snp | A/G | 1.66601e-05 | 0.00288614 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962547 | ATACTTACTCTTAGA[A/G]AAACCTGATTTACAA | 51136 |
rs762132274 | snp | A/C | 3.52783e-05 | 0.00419975 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954176 | AGTTCTGTTCATCTA[A/C]AAATTTCTTTCTTTC | 51136 |
rs762157565 | snp | A/C/G | 5.18276e-05 | 0.00509034 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962660 | AAAGAAAAAAAAATC[A/C/G]AAGAGGATTATATAA | 51136 |
rs762229184 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959035 | TTTGTCCAGTCCTGT[-/G]GTTTTTAAATATCAA | 51136 |
rs762556192 | in-del | -/A | 9.80857e-05 | 0.00700237 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964682 | CGCCTCCAGCCCTTC[-/A]AGTCGGGGCCATCAA | 51136 |
rs762600936 | snp | A/G | 0.000228337 | 0.0106825 | synonymous-codon, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964652 | CGGGAGCGACAGCAA[A/G]AACAGCGGCATACAC | 51136 |
rs762689295 | snp | A/G | 4.94189e-05 | 0.00497062 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963084 | GCACATTCTTTAGGT[A/G]TGGAGTTTATCTGGA | 51136 |
rs762781773 | snp | A/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956384 | AAGTAAAAGAAAAGG[A/T]TCATCTATTTATGAA | 51136 |
rs762817942 | snp | A/G | 1.65855e-05 | 0.00287967 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958274 | TCACTCCAATAAAGC[A/G]TAAGTGAGTTTCTTA | 51136 |
rs762857550 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957792 | GGAGGTTGCAGTGAG[C/T]CAAGATCACACCACT | 51136 |
rs762904326 | snp | C/G | 1.66941e-05 | 0.00288908 | missense | RNFT1 | GRCh38.p7 | 17:59958402 | AATCCAAAATACTTC[C/G]CAGAAGCTCAAATGG | 51136 |
rs763054055 | snp | A/G | 1.72761e-05 | 0.002939 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962808 | AATGAAAACAAGTCA[A/G]TGTTTTATTATGTCC | 51136 |
rs763301855 | snp | A/C | 1.9426e-05 | 0.0031165 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954035 | TTTTTAAATTTAAAA[A/C]TGTAATTACCTGACA | 51136 |
rs763553365 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954566 | GCTGGTTGAATGTAA[C/T]TCATGTGGAAAGCTT | 51136 |
rs763585978 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953304 | ACTGGTTCAAGTGAT[C/T]CTCCTGCCTCAGCCT | 51136 |
rs763689864 | in-del | -/TAAT | 1.91474e-05 | 0.00309408 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954037 | TTAAATTTAAAAATG[-/TAAT]TAATTACCTGACAAA | 51136 |
rs764078416 | snp | A/G | | | stop-gained | RNFT1 | GRCh38.p7 | 17:59956508 | GTGTAAAAAATATTC[A/G]TAAAACCTGTCTGAA | 51136 |
rs764112502 | snp | A/G | 1.68468e-05 | 0.00290226 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59958435 | CAAAGTAGGATTTAA[A/G]AAAATTAAGCTACCA | 51136 |
rs764154452 | snp | C/G | 3.24133e-05 | 0.00402562 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964618 | CTAACCTCTCATGAC[C/G]AGAAGCGGACGGAGG | 51136 |
rs764188730 | snp | A/T | 3.39968e-05 | 0.00412277 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956566 | AAGCTGAAAAGAGAA[A/T]TAAGAGATCATTTAT | 51136 |
rs764243343 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956127 | GTGAATAAGGAGTTA[A/C]TAGGAACAAACAAAG | 51136 |
rs764291863 | snp | C/G/T | 8.40165e-05 | 0.0064809 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962527 | TAATTTTTTAGTTGC[C/G/T]TGTTATACTTACTCT | 51136 |
rs764329459 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957716 | TGGGTGTGGTGGTGG[A/G]CACCTGTAATCCCAG | 51136 |
rs764375187 | in-del | -/AC | 8.79825e-05 | 0.00663201 | intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962504 | AATCTATGGAGAGAA[-/AC]AGTTAATAATTTTTT | 51136 |
rs764439764 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959378 | ACTCCAGTGAAACCA[-/G]GTCTTCTAATATTCT | 51136 |
rs764447891 | snp | C/G | 5.00739e-05 | 0.00500344 | missense | RNFT1 | GRCh38.p7 | 17:59954083 | TCTGAAATTCAGCTT[C/G]ACATATTGAACAAAT | 51136 |
rs764522395 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963071 | GCTTGCATTTTCTGC[A/G]CATTCTTTAGGTATG | 51136 |
rs764535671 | snp | G/T | 0.000244315 | 0.0110498 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954168 | AGATAGTAAGTTCTG[G/T]TCATCTACAAATTTC | 51136 |
rs764788789 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964529 | CCACGTCCGAGCCTC[C/G]AGTGCCTATTCTCCC | 51136 |
rs764837302 | snp | A/T | | | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962191 | TGCCCAGCCACTAAA[A/T]GTTTTTCATGATGAT | 51136 |
rs764930051 | snp | C/T | 8.23635e-05 | 0.00641677 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962950 | GATCTCCAGATTCTG[C/T]GGCAGTATCATCAGT | 51136 |
rs765045697 | snp | A/G | 2.93552e-05 | 0.00383102 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964632 | CCAGAAGCGGACGGA[A/G]GTGTCGGGAGCGACA | 51136 |
rs765062518 | snp | C/T | 1.65803e-05 | 0.00287922 | missense | RNFT1 | GRCh38.p7 | 17:59957309 | TAGCTTATAAGGTAG[C/T]GAAACCAAACTGGTA | 51136 |
rs765222525 | in-del | -/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953693 | TAACTGCTTAAGGTC[-/T]TTTGAGTTACTAGTA | 51136 |
rs765283827 | snp | A/G | 3.31818e-05 | 0.00407306 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958256 | TAATGTGATTCGATA[A/G]CATCACTCCAATAAA | 51136 |
rs765412498 | snp | C/T | 1.66388e-05 | 0.00288429 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962558 | TAGAAAAACCTGATT[C/T]ACAATGCTTTTGTTT | 51136 |
rs765434559 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959771 | AAAAATTTGCCAGGC[A/G]TGGTGGCGTGTGCCT | 51136 |
rs765452982 | in-del | -/CTCT | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958988 | ATGTCCAGTACTGGG[-/CTCT]CTATCTACACTCTCT | 51136 |
rs765486635 | in-del | -/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957849 | GAGACAATCTCAAAA[-/C]AAAACAAAACCAAAA | 51136 |
rs765505486 | snp | C/T | 5.08014e-05 | 0.00503965 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952926 | TGCCTTATCAGTAGT[C/T]ATTATGACCAAATGA | 51136 |
rs765593493 | snp | C/T | 1.65963e-05 | 0.0028806 | missense | RNFT1 | GRCh38.p7 | 17:59953068 | AGTGGACATGTTTTC[C/T]CTCTGTTAAACCATA | 51136 |
rs765646012 | snp | C/T | 1.67713e-05 | 0.00289575 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59956515 | AAATATTCGTAAAAC[C/T]TGTCTGAAAGTTCTC | 51136 |
rs765900698 | snp | A/T | 1.67122e-05 | 0.00289064 | missense | RNFT1 | GRCh38.p7 | 17:59960105 | GAAAGGTGTAATATA[A/T]AAGAACAGAAGATCC | 51136 |
rs765926024 | snp | G/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963087 | CATTCTTTAGGTATG[G/T]AGTTTATCTGGATAT | 51136 |
rs765945008 | snp | A/G | 3.29462e-05 | 0.00405857 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962985 | CTTGCTTCACTGTGG[A/G]AGTGACCCCGTAAGC | 51136 |
rs766052380 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966052 | AGCGCTTTGGAAGGC[C/T]GAGGCGGGAGGATCA | 51136 |
rs766162884 | snp | A/C | 1.65861e-05 | 0.00287972 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958277 | CTCCAATAAAGCATA[A/C]GTGAGTTTCTTACCT | 51136 |
rs766253181 | snp | C/G | 1.67103e-05 | 0.00289048 | missense | RNFT1 | GRCh38.p7 | 17:59958408 | AAATACTTCCCAGAA[C/G]CTCAAATGGTCCAAA | 51136 |
rs766553782 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953667 | AGGTGACACCTTTAA[G/T]ATTAAGTATGATAAC | 51136 |
rs766646042 | snp | A/G | 0.000280073 | 0.0118304 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964700 | TCGGGGCCATCAACC[A/G]CAAACCCCGCAAGCT | 51136 |
rs766723264 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957024 | GGTCGACTCCCCTTC[C/T]CTCCAGTGAAACCTG | 51136 |
rs766732641 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954619 | TTCCACACAATATCA[A/G]TTCACTAGGACCAGA | 51136 |
rs766860227 | snp | C/T | 1.70983e-05 | 0.00292384 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962819 | GTCAATGTTTTATTA[C/T]GTCCTACCTGTTATA | 51136 |
rs766977728 | in-del | -/GCAGCC | 1.67416e-05 | 0.00289318 | cds-indel | RNFT1 | GRCh38.p7 | 17:59954119 | CACATCTGAACACTG[-/GCAGCC]TCTCTTGCTGGCAGC | 51136 |
rs767055715 | snp | A/G | 1.68599e-05 | 0.00290338 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952943 | TTATGACCAAATGAC[A/G]TTAGTATTTTGTGGC | 51136 |
rs767058583 | snp | A/C | 3.36406e-05 | 0.00410112 | missense | RNFT1 | GRCh38.p7 | 17:59956539 | AGTTCTCAGATGCCC[A/C]AAAAATTCCAAAAGC | 51136 |
rs767347823 | snp | C/T | 3.31702e-05 | 0.00407235 | missense | RNFT1 | GRCh38.p7 | 17:59957254 | GAGTAAAGCCAGCAG[C/T]ATCCCAAGACTCCAT | 51136 |
rs767400966 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961462 | ATACTTTACACAGAC[A/G]TAGCCATTTAAAGTT | 51136 |
rs767479383 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956000 | CATGAACGTATTTAT[A/G]CACATATAATTGAGC | 51136 |
rs767521331 | in-del | -/C | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59952068 | GCATCTGTCTTGAAA[-/C]TTTTTTCTTTTAAAT | 51136 |
rs767522754 | snp | A/G | 8.44488e-05 | 0.00649748 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964711 | AACCGCAAACCCCGC[A/G]AGCTCTTCTCTCAGC | 51136 |
rs767617649 | snp | A/G | 1.6473e-05 | 0.00286988 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963101 | GGAGTTTATCTGGAT[A/G]TGAACATCTCCAGAA | 51136 |
rs767677025 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954245 | AATCTCCCTGGAACC[A/G]GGCATTTGAAAAACT | 51136 |
rs767839581 | snp | A/G | 0.000117228 | 0.00765509 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59958417 | CCAGAAGCTCAAATG[A/G]TCCAAAGTAGGATTT | 51136 |
rs767913140 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966233 | CGGAGGTTGCAGTGA[A/G]CTGAAATCGTGCCAC | 51136 |
rs767976996 | snp | A/G | 1.67565e-05 | 0.00289447 | missense | RNFT1 | GRCh38.p7 | 17:59954059 | CCTGACAAATGAGAA[A/G]AATTGGCTTCTGAAA | 51136 |
rs767989807 | snp | A/G | 1.64732e-05 | 0.0028699 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962942 | ACTACCATGATCTCC[A/G]GATTCTGCGGCAGTA | 51136 |
rs768021859 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955253 | TCAGAAATAAGTCAG[A/G]ATACTGTTAGATGAT | 51136 |
rs768029398 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965269 | TAGAGGACCCTACTG[C/T]CCTCAAAATAATTAT | 51136 |
rs768041185 | in-del | -/TTTC | 3.53313e-05 | 0.00420291 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954180 | CTGTTCATCTACAAA[-/TTTC]TTTCTTTCCTGTTCC | 51136 |
rs768048076 | snp | A/G | 1.66651e-05 | 0.00288657 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59953100 | GGTCATGCACTCTTC[A/G]CAAAATATATGCTGT | 51136 |
rs768168196 | in-del | -/C | 0.000133447 | 0.00816735 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59960111 | TGTAATATAAAAGAA[-/C]AGAAGATCCTGCTAA | 51136 |
rs768293150 | in-del | -/T | 1.66076e-05 | 0.00288158 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59958338 | CAATAAAATAAGGCA[-/T]TTTTAAGCCCATGAA | 51136 |
rs768376325 | snp | A/T | 1.65932e-05 | 0.00288034 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958248 | AATAGCATTAATGTG[A/T]TTCGATAACATCACT | 51136 |
rs768399969 | in-del | -/G | 1.73387e-05 | 0.00294432 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962665 | AAAAAAAATCAAAGA[-/G]GATTATATAAGCTAA | 51136 |
rs768524385 | snp | G/T | 2.34585e-05 | 0.00342472 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954007 | CAAGTCACAGAGAAC[G/T]GTTGTATTTAGGTTT | 51136 |
rs768584314 | snp | G/T | 1.70606e-05 | 0.00292062 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962644 | AAGTTCCAGTTAATT[G/T]AAAGAAAAAAAAATC | 51136 |
rs768597776 | snp | A/G | 1.65825e-05 | 0.00287941 | missense | RNFT1 | GRCh38.p7 | 17:59953038 | TTTATATGGTCTGAA[A/G]TCACAGTTCTGCAGA | 51136 |
rs768651836 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957091 | CCATTTCTAAACAAA[C/T]ATAGAACCTGCTATT | 51136 |
rs768674174 | snp | C/T | 1.65386e-05 | 0.00287559 | synonymous-codon, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962873 | CAGAATCAAAATATA[C/T]GGAAGACTTTTTTGC | 51136 |
rs768699257 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959411 | TAAAAGCTGAAAATT[C/T]AGAATACTCCCATTT | 51136 |
rs768705641 | snp | A/T | 1.67944e-05 | 0.00289775 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957214 | TGACAAGATTTGTAA[A/T]GTTACCTACTTTTAA | 51136 |
rs768723367 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959655 | GGCTGGGTGCAGTGG[C/T]TCACACCTGTAATCC | 51136 |
rs768994695 | snp | C/T | 9.88354e-05 | 0.00702908 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963166 | GGACACACTGAGGGG[C/T]TGAGGCATCCTCACT | 51136 |
rs769109342 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958532 | TGCTACAAATATTTT[A/G]TTTTGATATGTAAAA | 51136 |
rs769189847 | snp | C/T | 1.68057e-05 | 0.00289872 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59956506 | TTGTGTAAAAAATAT[C/T]CGTAAAACCTGTCTG | 51136 |
rs769443978 | snp | A/C | 0.000182266 | 0.00954461 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958730 | AAACTCATCAATACC[A/C]GACATCTGCTGTGTT | 51136 |
rs769465557 | in-del | -/TG | 0.000183503 | 0.00957694 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958740 | ATACCAGACATCTGC[-/TG]TGTTTTTCTTAACCA | 51136 |
rs769553226 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965803 | TGGCCACATCCTGGC[C/T]AATATGGTGAAACCC | 51136 |
rs769586740 | snp | C/T | | | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59956545 | CAGATGCCCAAAAAA[C/T]TCCAAAAGCTGAAAA | 51136 |
rs769590656 | in-del | -/GACCCA | 3.32906e-05 | 0.00407973 | cds-indel, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963252 | AAATACTTTTTCTCT[-/GACCCA]GATGTCTTTGCTTCA | 51136 |
rs769694876 | snp | C/T | 2.28162e-05 | 0.00337751 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954016 | GAGAACTGTTGTATT[C/T]AGGTTTTTAAATTTA | 51136 |
rs769733767 | in-del | -/GTG | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964262 | TCCCAGGACTGAACA[-/GTG]GTGCAGTCACCGTGT | 51136 |
rs769934619 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961253 | ATGTTGCCCAGGCTC[A/G]TCTTCAATTCCTGGG | 51136 |
rs770065555 | snp | G/T | 0.000572173 | 0.0169044 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964577 | CGGCCCCTCGCCGCC[G/T]CCTCCTCTGCCCGCT | 51136 |
rs770155911 | snp | A/G | 1.66322e-05 | 0.00288371 | missense | RNFT1 | GRCh38.p7 | 17:59957235 | CTACTTTTAATATGA[A/G]GTAGAGTAAAGCCAG | 51136 |
rs770376798 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957391 | AGTAACCCTAAAAAA[G/T]AAGAAGAAAACAAAT | 51136 |
rs770443593 | snp | A/G | 3.32806e-05 | 0.00407912 | missense | RNFT1 | GRCh38.p7 | 17:59960143 | AATACCAGTAACCAA[A/G]CACACTGAATCTTTG | 51136 |
rs770679705 | snp | A/G | 3.29571e-05 | 0.00405924 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963200 | TCCAGTTCCTGGAGG[A/G]CTGTGCAGTTGGCTA | 51136 |
rs770925636 | snp | C/T | 1.69775e-05 | 0.0029135 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960030 | TGAAATATATGATTA[C/T]ATTAAAAATGTAATT | 51136 |
rs770971055 | in-del | -/A | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957032 | CCCTTCCCTCCAGTG[-/A]AAACCTGAGGACCGC | 51136 |
rs771175584 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956938 | ATTATGTGTATGACA[A/G]TGTTACTGTTGAGGA | 51136 |
rs771297149 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965328 | AGGTTATTAAGAAAA[C/T]GAAGTTTAGGTCGGG | 51136 |
rs771440145 | snp | A/G | 3.63577e-05 | 0.00426351 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957400 | AAAAAATAAGAAGAA[A/G]ACAAATAGAGCTACC | 51136 |
rs771467874 | snp | C/T | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952667 | TGAGTTCTCTAAAAC[C/T]ACTAGTTCTAATTTC | 51136 |
rs771494966 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955772 | GCATTCTTTTAAGTC[A/G]GTCTCCTTGGGCCCT | 51136 |
rs771526006 | snp | C/G | 1.66477e-05 | 0.00288506 | missense | RNFT1 | GRCh38.p7 | 17:59958372 | GAATTTCAGAATGAA[C/G]TCTGTAATTCCAACA | 51136 |
rs771557590 | snp | C/T | 1.65866e-05 | 0.00287976 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59953013 | TGAAGTGGCTCCATC[C/T]TTCCATTTGTTTATA | 51136 |
rs771633041 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954192 | AAATTTCTTTCTTTC[C/T]TGTTCCTCAAATTAC | 51136 |
rs771898540 | in-del | -/CATT | 1.68728e-05 | 0.0029045 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952941 | ATTATGACCAAATGA[-/CATT]CATTAGTATTTTGTG | 51136 |
rs771916902 | snp | A/T | 3.26227e-05 | 0.0040386 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964683 | CGCCTCCAGCCCTTC[A/T]GTCGGGGCCATCAAC | 51136 |
rs771944480 | snp | A/T | 1.68335e-05 | 0.00290111 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962627 | AATTCCTGTTAGAAA[A/T]TAAGTTCCAGTTAAT | 51136 |
rs771969659 | in-del | -/TTAAC | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956651 | CATCAAATCCTCATA[-/TTAAC]TTAATGTTCATTATA | 51136 |
rs771997878 | snp | C/T | 1.66829e-05 | 0.00288811 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960181 | TTCCTGAAAGATAAA[C/T]AATTTTATAATGTTA | 51136 |
rs772021545 | in-del | -/AAG | 3.58339e-05 | 0.00423269 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957392 | GTAACCCTAAAAAAT[-/AAG]AAGAAAACAAATAGA | 51136 |
rs772057474 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960963 | AATATATGGGGTCTC[-/G]ACACATTGCTCAGAA | 51136 |
rs772154437 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963156 | AATCTTGTGTGGACA[C/G]ACTGAGGGGTTGAGG | 51136 |
rs772208453 | snp | A/G | 3.46081e-05 | 0.00415967 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954161 | TCTATGAAGATAGTA[A/G]GTTCTGTTCATCTAC | 51136 |
rs772559490 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59957104 | AATATAGAACCTGCT[A/G]TTACTTCAAACTAGT | 51136 |
rs772635440 | snp | A/G | 6.58903e-05 | 0.00573941 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963045 | TGGACACCTGACCTT[A/G]TATTTCTGGAGCTTG | 51136 |
rs772708702 | snp | C/T | 1.66874e-05 | 0.0028885 | missense | RNFT1 | GRCh38.p7 | 17:59958398 | CAACAATCCAAAATA[C/T]TTCCCAGAAGCTCAA | 51136 |
rs772808400 | in-del | -/A | 5.19404e-05 | 0.00509583 | splice-acceptor-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963286 | AGGCCTCTGTCTCCT[-/A]AAAAAATCAAATAAA | 51136 |
rs772914486 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953271 | CACCATCTCGGCTCA[C/T]TGCAACCTCCGCCCC | 51136 |
rs773080668 | snp | A/T | 2.13888e-05 | 0.00327016 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954025 | TGTATTTAGGTTTTT[A/T]AATTTAAAAATGTAA | 51136 |
rs773320224 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956951 | CAATGTTACTGTTGA[-/G]GATGGGTATGTTCTA | 51136 |
rs773378191 | snp | C/T | 3.35385e-05 | 0.00409489 | missense | RNFT1 | GRCh38.p7 | 17:59956516 | AATATTCGTAAAACC[C/T]GTCTGAAAGTTCTCA | 51136 |
rs773471559 | snp | A/T | 1.74048e-05 | 0.00294993 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962667 | AAAAAATCAAAGAGG[A/T]TTATATAAGCTAACA | 51136 |
rs773561530 | snp | A/T | 1.65971e-05 | 0.00288067 | missense | RNFT1 | GRCh38.p7 | 17:59953070 | TGGACATGTTTTCTC[A/T]CTGTTAAACCATAAG | 51136 |
rs773643112 | snp | C/T | 4.98691e-05 | 0.0049932 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964594 | CTCCTCTGCCCGCTT[C/T]CCCCAGGCCTAACCT | 51136 |
rs773788066 | snp | A/C | 1.6641e-05 | 0.00288448 | missense | RNFT1 | GRCh38.p7 | 17:59960148 | CAGTAACCAAGCACA[A/C]TGAATCTTTGAGGAC | 51136 |
rs773914914 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954489 | ATTATTTGACCCAGG[A/C]CTGCCAAATTGAGCT | 51136 |
rs773965750 | snp | G/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966151 | AATCACCCGGGCTTG[G/T]TGGCGGGCGCCTGTA | 51136 |
rs774034121 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959980 | AACTGAACTGAATAC[A/G]ATAAGTACTATGTGA | 51136 |
rs774062610 | in-del | -/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953949 | CCACTAAACACTAGA[-/T]TTTTTTTTTTTTGCC | 51136 |
rs774229103 | snp | G/T | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952911 | GAAAATCCATTCTGA[G/T]GCCTTATCAGTAGTC | 51136 |
rs774821490 | in-del | -/CG | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964772 | CCGGACGTTCTCACG[-/CG]CGCGCGCGCGCGCCC | 51136 |
rs774974182 | in-del | -/ATG | 1.69689e-05 | 0.00291275 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960023 | AGTGCTATGAAATAT[-/ATG]ATTACATTAAAAATG | 51136 |
rs775007562 | snp | G/T | 1.65831e-05 | 0.00287945 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59953025 | ATCCTTCCATTTGTT[G/T]ATATGGTCTGAAATC | 51136 |
rs775069218 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954288 | CAAACATCTCAAAGC[C/T]GAGCCATATACAGAA | 51136 |
rs775105064 | in-del | -/ATGGTCTGAA | 1.65833e-05 | 0.00287948 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59953028 | CTTCCATTTGTTTAT[-/ATGGTCTGAA]ATCACAGTTCTGCAG | 51136 |
rs775184436 | snp | C/T | 1.66101e-05 | 0.0028818 | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964608 | TCCCCCAGGCCTAAC[C/T]TCTCATGACCAGAAG | 51136 |
rs775198295 | snp | A/C | 5.00638e-05 | 0.00500294 | intron-variant | RNFT1 | GRCh38.p7 | 17:59960182 | TCCTGAAAGATAAAC[A/C]ATTTTATAATGTTAC | 51136 |
rs775270982 | snp | G/T | 1.65743e-05 | 0.00287869 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59957271 | TCCCAAGACTCCATC[G/T]AGTTACGTTACCAAA | 51136 |
rs775434436 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963666 | CATCTCTGATGTAGA[C/T]TCTACATCAAAGAAG | 51136 |
rs775473196 | in-del | -/GTTGGGATGACAGGCGTGAGCCCCTGTGCCTGGCCCAG | | | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59961842 | TGGGCCTCCCAGAGT[lengthTooLong]GTCTTTTTTTTTTTT | 51136 |
rs775481904 | snp | C/T | 3.46644e-05 | 0.00416305 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954163 | TATGAAGATAGTAAG[C/T]TCTGTTCATCTACAA | 51136 |
rs775541461 | in-del | -/A | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956267 | TATAAGCACTGCAAC[-/A]ATTAGCAGGTGGTTG | 51136 |
rs775559789 | snp | G/T | 1.65913e-05 | 0.00288017 | missense | RNFT1 | GRCh38.p7 | 17:59957250 | GGTAGAGTAAAGCCA[G/T]CAGTATCCCAAGACT | 51136 |
rs775567916 | snp | A/G | 1.69668e-05 | 0.00291258 | missense | RNFT1 | GRCh38.p7 | 17:59956490 | AAAAAGTACTTACTG[A/G]TTGTGTAAAAAATAT | 51136 |
rs775632598 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59961519 | ATCCTCTTTTTCCCA[A/G]TGATTTATATGACGG | 51136 |
rs775757786 | in-del | -/CG | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964771 | CCCCGGACGTTCTCA[-/CG]CGCGCGCGCGCGCCC | 51136 |
rs775874180 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962943 | CTACCATGATCTCCA[C/G]ATTCTGCGGCAGTAT | 51136 |
rs775935678 | snp | A/C | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959242 | CCACCATCCAGCCAG[A/C]TGCTTAGACTAAAAA | 51136 |
rs775964365 | snp | C/T | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963046 | GGACACCTGACCTTA[C/T]ATTTCTGGAGCTTGC | 51136 |
rs776136631 | in-del | -/AT | 1.66813e-05 | 0.00288797 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59954097 | TGACATATTGAACAA[-/AT]ATCATCCACATCTGA | 51136 |
rs776200811 | in-del | -/A | 1.68417e-05 | 0.00290182 | frameshift-variant | RNFT1 | GRCh38.p7 | 17:59958432 | TCCAAAGTAGGATTT[-/A]AAAAAAATTAAGCTA | 51136 |
rs776255005 | snp | C/T | 1.65935e-05 | 0.00288036 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958251 | AGCATTAATGTGATT[C/T]GATAACATCACTCCA | 51136 |
rs776311123 | snp | G/T | 3.31675e-05 | 0.00407218 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59953048 | CTGAAATCACAGTTC[G/T]GCAGAGTGGACATGT | 51136 |
rs776428391 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953447 | CTCAGGTGATCCACC[C/T]ACCTCAGCCTCCCAA | 51136 |
rs776488906 | snp | C/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965550 | AGAATCACTTGAACC[C/G]GGGAGGTGGAGTTTG | 51136 |
rs776632063 | snp | C/T | 1.67116e-05 | 0.0028906 | splice-donor-variant | RNFT1 | GRCh38.p7 | 17:59957223 | TTGTAATGTTACCTA[C/T]TTTTAATATGAGGTA | 51136 |
rs776709465 | in-del | -/A | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958938 | TGCTGGTTTCTTCTT[-/A]AGTCTCCTTTGCTGT | 51136 |
rs776820480 | snp | A/G | 3.29457e-05 | 0.00405854 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963073 | TTGCATTTTCTGCAC[A/G]TTCTTTAGGTATGGA | 51136 |
rs776898234 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959475 | AAGTGTTCTTACTTT[C/T]AGAAACAACGACCAA | 51136 |
rs777065627 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59953358 | GACCACCACCACCAT[A/G]CCCAGCTAGTTTTTT | 51136 |
rs777102208 | snp | A/G | 1.6476e-05 | 0.00287014 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963182 | TGAGGCATCCTCACT[A/G]CTTCCAGTTCCTGGA | 51136 |
rs777117173 | snp | C/T | 1.67992e-05 | 0.00289816 | missense | RNFT1 | GRCh38.p7 | 17:59956507 | TGTGTAAAAAATATT[C/T]GTAAAACCTGTCTGA | 51136 |
rs777288752 | in-del | -/CG | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964770 | CCCCGGACGTTCTCA[-/CG]CGCGCGCGCGCGCGC | 51136 |
rs777366933 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963004 | GACCCCGTAAGCGAC[C/T]GTGTACACATCCATG | 51136 |
rs777370580 | snp | C/T | 1.66402e-05 | 0.00288441 | stop-gained | RNFT1 | GRCh38.p7 | 17:59960140 | AAGAATACCAGTAAC[C/T]AAGCACACTGAATCT | 51136 |
rs777624367 | snp | C/T | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952389 | ATTTATTTTCACTTA[C/T]TACTAATCTTACTAC | 51136 |
rs777692720 | in-del | -/AGC | | | cds-indel, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962592 | TACATAAAAGTTGTT[-/AGC]AGCCCAATTCCAAGA | 51136 |
rs777737240 | snp | A/G | 1.6902e-05 | 0.00290701 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59954141 | GCTGGCAGCCACTCC[A/G]TAACTCTATGAAGAT | 51136 |
rs777825144 | snp | C/T | 1.76036e-05 | 0.00296673 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956467 | TGAAGGTGTTTTTCT[C/T]AACTGATAAAAAGTA | 51136 |
rs777855381 | snp | G/T | 1.6628e-05 | 0.00288335 | missense | RNFT1 | GRCh38.p7 | 17:59958357 | TAAGCCCATGAAAAA[G/T]AATTTCAGAATGAAG | 51136 |
rs777873141 | in-del | -/GAAAAGAGAA | 3.37764e-05 | 0.00410938 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956556 | AAAATTCCAAAAGCT[-/GAAAAGAGAA]ATAAGAGATCATTTA | 51136 |
rs777909901 | snp | G/T | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965268 | ATAGAGGACCCTACT[G/T]CCCTCAAAATAATTA | 51136 |
rs778140295 | snp | A/G | 7.20422e-05 | 0.00600133 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957394 | AACCCTAAAAAATAA[A/G]AAGAAAACAAATAGA | 51136 |
rs778209008 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958246 | TAAATAGCATTAATG[G/T]GATTCGATAACATCA | 51136 |
rs778417580 | snp | G/T | 1.66649e-05 | 0.00288655 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962596 | TAAAAGTTGTTAGCA[G/T]CCCAATTCCAAGAGA | 51136 |
rs778421039 | snp | C/T | 1.67184e-05 | 0.00289118 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964714 | CGCAAACCCCGCAAG[C/T]TCTTCTCTCAGCCCG | 51136 |
rs778507419 | snp | C/T | 3.33962e-05 | 0.0040862 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962840 | ACCTGTTATATGCTG[C/T]ATAACAAGTTTGACG | 51136 |
rs778507676 | snp | A/G | 1.65965e-05 | 0.00288062 | missense | RNFT1 | GRCh38.p7 | 17:59952997 | ATATTTGAAGGTGTG[A/G]TGAAGTGGCTCCATC | 51136 |
rs778516258 | snp | A/C | 1.72074e-05 | 0.00293316 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956479 | TCTTAACTGATAAAA[A/C]GTACTTACTGGTTGT | 51136 |
rs778578185 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960677 | AGTTAGCCAGGCGCC[A/G]TGGCACGTGCCTGTA | 51136 |
rs778597257 | snp | A/T | 1.69942e-05 | 0.00291493 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953129 | GTAATGGAATTAAGA[A/T]TTAGATTTGATATTT | 51136 |
rs778670963 | snp | C/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59954927 | TCTCTAAGATTTTAA[C/G]CTCCTCACCAGATTC | 51136 |
rs778713054 | snp | A/G | 1.67125e-05 | 0.00289067 | | | GRCh38.p7 | 17:59963261 | TTCTCTGACCCAGAT[A/G]TCTTTGCTTCAGGCC | 51136 |
rs778793460 | in-del | -/A | 5.1577e-05 | 0.00507797 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956588 | ATCATTTATTAATTC[-/A]AACAGTCCTATTTGC | 51136 |
rs778800756 | snp | G/T | 1.74891e-05 | 0.00295707 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956599 | ATTCAAACAGTCCTA[G/T]TTGCTAAACCCAAAA | 51136 |
rs778825983 | snp | G/T | | | upstream-variant-2KB, intron-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59966409 | TTCTGACAGATTTCT[G/T]GTTCAGTAAGGGTGA | 51136 |
rs778918130 | in-del | -/A | 3.32817e-05 | 0.00407919 | frameshift-variant, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962581 | TTTGTTTGCATACAT[-/A]AAAAGTTGTTAGCAG | 51136 |
rs778998844 | snp | C/T | 1.64727e-05 | 0.00286986 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963136 | GGCAAGAACCCTCTC[C/T]TGTCAATCTTGTGTG | 51136 |
rs779146158 | snp | A/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59958789 | ATCTCTTCCTTTCAA[A/T]GAATTGCTTGTCAAG | 51136 |
rs779222056 | snp | G/T | | | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952605 | TGTATCTTAAAATAT[G/T]ATGAAAAATATTCTT | 51136 |
rs779232865 | snp | A/G | | | upstream-variant-2KB, intron-variant | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59965410 | GGTCACTTGAGCTCA[A/G]GAGGTAGAGACCAGC | 51136 |
rs779444337 | snp | C/T | 1.66499e-05 | 0.00288525 | missense | RNFT1 | GRCh38.p7 | 17:59958373 | AATTTCAGAATGAAG[C/T]CTGTAATTCCAACAA | 51136 |
rs779461386 | snp | C/T | 2.39512e-05 | 0.0034605 | intron-variant | RNFT1 | GRCh38.p7 | 17:59953999 | GACTTTTGCAAGTCA[C/T]AGAGAACTGTTGTAT | 51136 |
rs779532271 | snp | A/G | 1.71009e-05 | 0.00292406 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958466 | AAAGAAAAACATCAA[A/G]ATTTATCAGAGCAAC | 51136 |
rs779534495 | in-del | -/AGTC | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955247 | AAGATTTCAGAAATA[-/AGTC]AGGATACTGTTAGAT | 51136 |
rs779603902 | in-del | -/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955041 | TTCTGTAGAAATGAT[-/G]GGGAAGAGGTAACTA | 51136 |
rs779733197 | snp | C/T | 3.33734e-05 | 0.0040848 | missense | RNFT1 | GRCh38.p7 | 17:59954103 | ATTGAACAAATATCA[C/T]CCACATCTGAACACT | 51136 |
rs779789449 | in-del | -/AAAT | 1.82777e-05 | 0.003023 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957403 | AAATAAGAAGAAAAC[-/AAAT]AGAGCTACCCAAACT | 51136 |
rs779805446 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59955116 | AGCATGACTTAACAT[A/G]GCTGAAGTTATCTAA | 51136 |
rs779864991 | in-del | -/T | 1.72403e-05 | 0.00293596 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962658 | TGAAAGAAAAAAAAA[-/T]CAAAGAGGATTATAT | 51136 |
rs780038172 | snp | C/G | 1.68929e-05 | 0.00290623 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962631 | CCTGTTAGAAAATAA[C/G]TTCCAGTTAATTGAA | 51136 |
rs780040800 | snp | C/G | 1.64732e-05 | 0.0028699 | missense, nc-transcript-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963158 | TCTTGTGTGGACACA[C/G]TGAGGGGTTGAGGCA | 51136 |
rs780077926 | snp | A/G | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956194 | CATAAGATTGTTAAG[A/G]GTTTACAAGCCTTAA | 51136 |
rs780128550 | snp | A/G | 1.77015e-05 | 0.00297497 | intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59963304 | AAAATCAAATAAAAG[A/G]TATTCTAAGTAAACA | 51136 |
rs780217967 | snp | G/T | 1.6859e-05 | 0.00290331 | intron-variant | RNFT1 | GRCh38.p7 | 17:59957205 | ATCATGCAGTGACAA[G/T]ATTTGTAATGTTACC | 51136 |
rs780311442 | snp | A/G | 1.66394e-05 | 0.00288434 | stop-gained | RNFT1 | GRCh38.p7 | 17:59957340 | TGGGAACAAAAGTTC[A/G]GTAGTATTGACACAA | 51136 |
rs780408706 | snp | G/T | 4.63381e-05 | 0.0048132 | intron-variant | RNFT1 | GRCh38.p7 | 17:59958635 | AAACCTGTTTGGATT[G/T]TAGATCTTCCCTTCA | 51136 |
rs780465050 | snp | C/T | | | downstream-variant-500B | RNFT1 | GRCh38.p7 | 17:59951919 | CTAGAGGCGAACAAA[C/T]CACACTATCAAAACC | 51136 |
rs780547372 | snp | C/T | | | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962010 | CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGAATA | 51136 |
rs780563641 | snp | C/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59956324 | ACAGAGATAAAACTC[C/T]TAAATTATTATAGCC | 51136 |
rs780754444 | snp | G/T | 1.79191e-05 | 0.00299319 | intron-variant | RNFT1 | GRCh38.p7 | 17:59956458 | GAAGAAAGGTGAAGG[G/T]GTTTTTCTTAACTGA | 51136 |
rs780862855 | in-del | -/A | 1.70813e-05 | 0.00292239 | intron-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962820 | CAATGTTTTATTATG[-/A]TCCTACCTGTTATAT | 51136 |
rs780954490 | snp | A/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959004 | TCTCTATCTACACTC[A/T]CTTTCCTGGGTTAGT | 51136 |
rs781046257 | snp | A/T | 6.68393e-05 | 0.00578059 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59954111 | AATATCATCCACATC[A/T]GAACACTGTCTCTTG | 51136 |
rs781150847 | snp | C/T | 2.33653e-05 | 0.00341791 | intron-variant | RNFT1 | GRCh38.p7 | 17:59954009 | AGTCACAGAGAACTG[C/T]TGTATTTAGGTTTTT | 51136 |
rs781156171 | snp | G/T | 1.65168e-05 | 0.00287369 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962881 | AAATATATGGAAGAC[G/T]TTTTTGCAGCCACTT | 51136 |
rs781242995 | snp | A/T | 1.65847e-05 | 0.0028796 | missense | RNFT1 | GRCh38.p7 | 17:59958298 | TTTCTTACCTTAGAT[A/T]TAAAAGGCATGATGA | 51136 |
rs781274048 | snp | A/T | 5.97496e-05 | 0.00546546 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964664 | CAAGAACAGCGGCAT[A/T]CACCGCCTCCAGCCC | 51136 |
rs781278705 | snp | A/G | 1.71581e-05 | 0.00292895 | synonymous-codon | RNFT1 | GRCh38.p7 | 17:59957371 | TTCTTCTAAAAGCAT[A/G]TACCAGTAACCCTAA | 51136 |
rs781445606 | snp | C/T | 3.34448e-05 | 0.00408917 | utr-variant-3-prime | RNFT1 | GRCh38.p7 | 17:59952964 | ATTTTGTGGCCTTGA[C/T]AGTTTATACAACTTA | 51136 |
rs781480128 | snp | C/T | 1.66313e-05 | 0.00288364 | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59962569 | GATTTACAATGCTTT[C/T]GTTTGCATACATAAA | 51136 |
rs781691875 | snp | A/G | | | missense, nc-transcript-variant | RNFT1, TBC1D3P1-DHX40P1 | GRCh38.p7 | 17:59963001 | AGTGACCCCGTAAGC[A/G]ACTGTGTACACATCC | 51136 |
rs796077019 | snp | C/G | | | missense, intron-variant, upstream-variant-2KB | RNFT1, TBC1D3P1-DHX40P1, LOC101927755 | GRCh38.p7 | 17:59964660 | ACAGCAAGAACAGCG[C/G]CATACACCGCCTCCA | 51136 |
rs796172851 | in-del | -/TT | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960472 | GAAAATTAAATTAAA[-/TT]AAAAAAAAAAAAAAG | 51136 |
rs796907121 | multinucleotide-polymorphism | GA/TT | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59960457 | AAAAAAAAAAAAAAG[GA/TT]AATTAAATTAAATTA | 51136 |
rs796981140 | snp | G/T | | | intron-variant | RNFT1 | GRCh38.p7 | 17:59959810 | AGCTACTCAGGAGGC[G/T]TAGACGGGAGAATTG | 51136 |