SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs12448 | snp | A/G | 0.324382 | 0.238678 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512405 | AGCTCCAAGACACTT[A/G]CTGATCTACTGTGAA | 50862 |
rs1043778 | snp | A/G | 0 | 0 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513267 | AAATCAATTTCAAGG[A/G]AAAACATCTGGCCAG | 50862 |
rs1047730 | snp | A/G | 0.367913 | 0.220446 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514751 | AAAAATAAACTTCCC[A/G]TGTCTTCCATTTGTG | 50862 |
rs1065052 | snp | C/T | 0.48196 | 0.0932449 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10534042 | TTATGAAGAATTTCT[C/T]GGGAGAGTAGCTGAG | 50862 |
rs1074375 | snp | A/G | 0.497803 | 0.033074 | intron-variant | RNF141 | GRCh38.p7 | 11:10517312 | GAGATAGCAATAGTA[A/G]CTATCCAGGATGAAA | 50862 |
rs1074376 | snp | C/G | 0.0263992 | 0.111815 | intron-variant | RNF141 | GRCh38.p7 | 11:10517332 | CCAGGATGAAACCCA[C/G]AGAAAGACTCAAAAA | 50862 |
rs1074377 | snp | A/G | 0.493154 | 0.0581045 | intron-variant | RNF141 | GRCh38.p7 | 11:10517727 | CATACTGAAAGAAAA[A/G]ATACTCTCAAGTCTA | 50862 |
rs1350991 | snp | C/T | 0.378174 | 0.214642 | intron-variant | RNF141 | GRCh38.p7 | 11:10533083 | TAAGAGGTGACTCCA[C/T]AGGTTCTAATTATAC | 50862 |
rs1462940 | snp | G/T | 0.16846 | 0.236329 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541389 | AGTCTCGCCTGTCAC[G/T]CTCCCGGAGCAGGGG | 50862 |
rs1462941 | snp | G/T | 0.317933 | 0.240593 | upstream-variant-2KB, splice-donor-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541543 | CAGTTGGGCTCCAAG[G/T]TACCACTTCCCAGAC | 50862 |
rs1462942 | snp | C/G | 0.0126979 | 0.078662 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541578 | AGCCTCCCCACTGAT[C/G]ATAGATACACAAAGG | 50862 |
rs1531479 | snp | C/T | 0.465788 | 0.126237 | intron-variant | RNF141 | GRCh38.p7 | 11:10535383 | CAAAAAACAACAGTT[C/T]TGAATCTGAGCCTAC | 50862 |
rs1841811 | snp | A/G | 0.416218 | 0.186739 | intron-variant | RNF141 | GRCh38.p7 | 11:10524333 | CTGCCTCCCGGGTTC[A/G]CGCCATTCTCCTGCC | 50862 |
rs1979367 | snp | A/T | 0.130351 | 0.219509 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541509 | ACCAAGGCCGCACTG[A/T]GAGCCCTGGTTTGGT | 50862 |
rs1993817 | snp | C/T | 0.497722 | 0.0336691 | intron-variant | RNF141 | GRCh38.p7 | 11:10518592 | AATACATGTAGTTTA[C/T]TGTATGTATTTTATA | 50862 |
rs1993818 | snp | A/C | 0.497695 | 0.0338674 | intron-variant | RNF141 | GRCh38.p7 | 11:10518784 | TTTGATTTTAGACTT[A/C]AGTCAGGCACAAATT | 50862 |
rs1993819 | snp | A/G | 0.497359 | 0.0362457 | intron-variant | RNF141 | GRCh38.p7 | 11:10518796 | CTTAAGTCAGGCACA[A/G]ATTTTCATACAGCAA | 50862 |
rs1993820 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF141 | GRCh38.p7 | 11:10535720 | TTATAAGTTCTTTTT[A/G]AGATTTTTGTTAAGT | 50862 |
rs2054390 | snp | C/T | 0.367708 | 0.220556 | intron-variant | RNF141 | GRCh38.p7 | 11:10528704 | ATAAACAAGGAAAGC[C/T]TCAACCTATCCCAGT | 50862 |
rs2054391 | snp | A/C | 0.370365 | 0.219117 | intron-variant | RNF141 | GRCh38.p7 | 11:10535961 | ATTCAACAAGTAGCA[A/C]gtgcctggtgcttat | 50862 |
rs2054392 | snp | C/G | 0.473081 | 0.112848 | intron-variant | RNF141 | GRCh38.p7 | 11:10537052 | AGTTTGTTTAAATAT[C/G]TGAGGAGCTGTCATG | 50862 |
rs3074399 | in-del | -/CA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10534501 | acacacacacacaca[-/CA]CGCATTCAAGTAATT | 50862 |
rs3075189 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542808 | AAAAAAAAAAAAAAA[-/AA]GCAGCAAATTTGGGA | 50862 |
rs3177103 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513278 | AAATAAAATTCAAAT[C/T]AATTTCAAGGAAAAA | 50862 |
rs3781862 | snp | A/G | 0.399611 | 0.200291 | intron-variant | RNF141 | GRCh38.p7 | 11:10538802 | ATTAATTTAATGACA[A/G]ATTTTCACAGTTTTA | 50862 |
rs3781863 | snp | C/T | 0.477515 | 0.103619 | intron-variant | RNF141 | GRCh38.p7 | 11:10538561 | CTCACTAGAGGGAAA[C/T]GGCCAAGTGACTTAA | 50862 |
rs3943326 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF141 | GRCh38.p7 | 11:10517968 | tatgaaatacttggg[A/G]atagatgtcaaagat | 50862 |
rs4146830 | snp | C/T | 0.406986 | 0.194565 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514569 | GAGTATTCTGGAATC[C/T]TTTTACTTAGATATA | 50862 |
rs4243915 | snp | A/G | 0.422473 | 0.180978 | intron-variant | RNF141 | GRCh38.p7 | 11:10523857 | CCACTATTCTGGAGA[A/G]AAGAAAAGCAGAAAA | 50862 |
rs4909936 | snp | A/C | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10518164 | gtaaaatggcacaag[A/C]ctgctttggaaaata | 50862 |
rs4909937 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | RNF141 | GRCh38.p7 | 11:10518339 | gataaatatggaaaa[C/T]aatctaatttccctc | 50862 |
rs4909938 | snp | C/T | 0.367091 | 0.220884 | intron-variant | RNF141 | GRCh38.p7 | 11:10520066 | gggctgcatgcagcc[C/T]gtgggccgtgagttg | 50862 |
rs4909939 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | RNF141 | GRCh38.p7 | 11:10520428 | acagcgtcaggatca[C/T]caccatcactgtctt | 50862 |
rs4909940 | snp | C/T | 0.365232 | 0.22186 | intron-variant | RNF141 | GRCh38.p7 | 11:10521749 | TTCTAGGTGCATAAA[C/T]AAAGTTGTAGAGGTA | 50862 |
rs4909941 | snp | C/T | 0.35445 | 0.227135 | intron-variant | RNF141 | GRCh38.p7 | 11:10536978 | ACATATTCATGGGCA[C/T]AGAAAAAAAAAGAGG | 50862 |
rs4909942 | snp | G/T | 0.327914 | 0.237549 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540593 | GCCTAAGCCAATTCA[G/T]AAGTGTGGGGCTGGC | 50862 |
rs4910149 | snp | A/C | 0.367913 | 0.220446 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511509 | GGGTGAATAGACATA[A/C]GAACAAATGAGTCTG | 50862 |
rs4910150 | snp | C/T | 0.367913 | 0.220446 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511626 | TAGTTTTCTTATTCC[C/T]GGATAGACTAAGCTT | 50862 |
rs4910151 | snp | A/G | 0.365439 | 0.221752 | intron-variant | RNF141 | GRCh38.p7 | 11:10524272 | TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC | 50862 |
rs4910152 | snp | C/G | 0.416055 | 0.186885 | intron-variant | RNF141 | GRCh38.p7 | 11:10530475 | AGCAATTAGACAACT[C/G]TAAGATTCAAACAGC | 50862 |
rs4910153 | snp | C/T | 0.499908 | 0.00678851 | intron-variant | RNF141 | GRCh38.p7 | 11:10531808 | ATAAAATGAGGCCAT[C/T]GAAAGTTAAGCAACT | 50862 |
rs4910154 | snp | C/T | 0.378174 | 0.214642 | intron-variant | RNF141 | GRCh38.p7 | 11:10532125 | TGCTAAAGGGCAAAA[C/T]TTCATACAATAGACA | 50862 |
rs4910155 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | RNF141 | GRCh38.p7 | 11:10532128 | TAAAGGGCAAAACTT[C/T]ATACAATAGACAGGG | 50862 |
rs6484344 | snp | C/T | 0.498459 | 0.0277128 | intron-variant | RNF141 | GRCh38.p7 | 11:10515177 | AATAGCATAGAAATA[C/T]ATAGTGAAAAATAAA | 50862 |
rs7112744 | snp | A/T | 0.181022 | 0.240296 | intron-variant | RNF141 | GRCh38.p7 | 11:10536324 | TTGAGGTAATTTTTA[A/T]AAAGGCCACAAGGAC | 50862 |
rs7115413 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | RNF141 | GRCh38.p7 | 11:10515388 | gcacctgttagagct[A/G]tttattctttttaac | 50862 |
rs7123581 | snp | A/C | 0.365853 | 0.221536 | intron-variant | RNF141 | GRCh38.p7 | 11:10522377 | CCAGTGGAACCAGTA[A/C]AAAGTTCTCTTAACT | 50862 |
rs7126551 | snp | G/T | 0.370772 | 0.218893 | intron-variant | RNF141 | GRCh38.p7 | 11:10536336 | TTAAAAAGGCCACAA[G/T]GACTAAAGCAGAGAG | 50862 |
rs7128848 | snp | A/G | 0.358515 | 0.225221 | intron-variant | RNF141 | GRCh38.p7 | 11:10538236 | TCACTAACTCCTTGC[A/G]TTAAAATGCAACAGT | 50862 |
rs7129207 | snp | A/C | 0.304937 | 0.243889 | intron-variant | RNF141 | GRCh38.p7 | 11:10532537 | CACACACACACACAC[A/C]CCCCACAACTATATA | 50862 |
rs7131507 | snp | A/T | 0.239037 | 0.24976 | intron-variant | RNF141 | GRCh38.p7 | 11:10537801 | CTAGGAAGATAAGGG[A/T]TACTTTAAGAAGGCT | 50862 |
rs7929890 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513802 | CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGATTAC | 50862 |
rs7934688 | snp | A/C | 0.123452 | 0.215605 | intron-variant | RNF141 | GRCh38.p7 | 11:10528863 | tgccctcaggagctt[A/C]ctctctaaaggggag | 50862 |
rs7936626 | snp | C/T | 0.367297 | 0.220775 | intron-variant | RNF141 | GRCh38.p7 | 11:10533337 | TTAACAAATAGAAGA[C/T]TAAGTTGTATTAGGT | 50862 |
rs7938430 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536878 | GCAGCCTACTAGTCC[A/G]TTATGCTTTGCAATG | 50862 |
rs7938782 | snp | A/G | 0.354235 | 0.227234 | intron-variant | RNF141 | GRCh38.p7 | 11:10537230 | AGTATGGAAGTGTTT[A/G]GGTAAAGATTAGAAG | 50862 |
rs7949992 | snp | A/G | 0.130351 | 0.219509 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541723 | TAGATATGATGATGA[A/G]CACATGTTAGTGATA | 50862 |
rs7950829 | snp | C/G | 0.130351 | 0.219509 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541726 | ATATGATGATGAGCA[C/G]ATGTTAGTGATATTA | 50862 |
rs7951653 | snp | A/T | 0.498503 | 0.0273153 | intron-variant | RNF141 | GRCh38.p7 | 11:10520154 | atgaacactgtacat[A/T]taggctatacgaaat | 50862 |
rs9300104 | snp | C/T | 0.416055 | 0.186885 | intron-variant | RNF141 | GRCh38.p7 | 11:10529559 | TAGTTTGGAGTCATA[C/T]TGTAGGAGTTGGGAC | 50862 |
rs9665807 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10537533 | ggagatagaatttct[C/T]tccctctgctctctg | 50862 |
rs10458930 | snp | C/G | 0.416708 | 0.186302 | intron-variant | RNF141 | GRCh38.p7 | 11:10527921 | tcacttacagattgt[C/G]aggtgtgagagacaa | 50862 |
rs10458931 | snp | A/G | 0.416708 | 0.186302 | intron-variant | RNF141 | GRCh38.p7 | 11:10527926 | tacagattgtcaggt[A/G]tgagagacaaagaaa | 50862 |
rs10500725 | snp | A/G | 0.421051 | 0.182323 | intron-variant | RNF141 | GRCh38.p7 | 11:10516174 | TCTAGTTCTTCAGAG[A/G]TATTTTACAAGATAA | 50862 |
rs10500726 | snp | A/T | 0.496937 | 0.0390173 | intron-variant | RNF141 | GRCh38.p7 | 11:10528900 | ACCTAAACAACTTTT[A/T]TCGTAATGCAGTATT | 50862 |
rs10500727 | snp | C/T | 0.18134 | 0.240387 | intron-variant | RNF141 | GRCh38.p7 | 11:10531777 | AGTGGGGATATCACA[C/T]TCAACTAACAGCTAA | 50862 |
rs10524171 | in-del | -/T/TATATATATATAT/TATATATATATATATATATAT | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539701 | TATATATATATATTA[lengthTooLong]GAGAGAGAAGGAGAG | 50862 |
rs10559393 | in-del | -/CA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532498 | TTTCTACACACACAC[-/CA]ACACACACACACACA | 50862 |
rs10602390 | in-del | -/TGAA | 0.357664 | 0.225629 | intron-variant | RNF141 | GRCh38.p7 | 11:10518467 | CCAAGGTAATTAGAC[-/TGAA]TGAAAGAAGCCAGAC | 50862 |
rs10664382 | in-del | -/A/AA/AAA | 0.625 | 0.125 | intron-variant | RNF141 | GRCh38.p7 | 11:10531388 | CAAAAAAAAAAAAAA[-/A/AA/AAA]GGTTAGCTAGTGTCA | 50862 |
rs10743143 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | RNF141 | GRCh38.p7 | 11:10523305 | TAGGTTAGAGCACAG[C/T]TGTACTGCCAGACAG | 50862 |
rs10770123 | snp | C/T | 0.498568 | 0.0267188 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513319 | TAAAATCCTACTATC[C/T]AGAAATTCTGTCATC | 50862 |
rs10770124 | snp | A/G | 0.354665 | 0.227036 | intron-variant | RNF141 | GRCh38.p7 | 11:10538943 | AATTCAACAAAAGAT[A/G]AATTTCTGGTCAAGA | 50862 |
rs10840432 | snp | A/G | 0.323197 | 0.239044 | intron-variant | RNF141 | GRCh38.p7 | 11:10524166 | atgcctgtaatccca[A/G]cactctgggaggccg | 50862 |
rs10840433 | snp | C/G | 0.416218 | 0.186739 | intron-variant | RNF141 | GRCh38.p7 | 11:10525627 | TTAATTAGGCATTAT[C/G]CTGTTGATGGGTAAG | 50862 |
rs10840434 | snp | A/T | 0.416382 | 0.186593 | intron-variant | RNF141 | GRCh38.p7 | 11:10534894 | TTAAAAATATATAAA[A/T]AGACTTGTGGCTTGA | 50862 |
rs10840435 | snp | C/G | 0.482083 | 0.0929373 | intron-variant | RNF141 | GRCh38.p7 | 11:10536299 | TGAGACAGGAAGCAG[C/G]ACGGTGACTTTGAGG | 50862 |
rs10840436 | snp | C/T | 0.498568 | 0.0267188 | intron-variant | RNF141 | GRCh38.p7 | 11:10536403 | TGTTTAACATTTTTG[C/T]TGATGACCTGAAGAC | 50862 |
rs10840437 | snp | C/T | 0.355954 | 0.226437 | intron-variant | RNF141 | GRCh38.p7 | 11:10538348 | GAAAACCATAAAATA[C/T]TGATAAATATTAACA | 50862 |
rs11042866 | snp | C/G | 0.312593 | 0.242037 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511606 | TAACTTCCCTCATCT[C/G]CAAGTAGTTTTCTTA | 50862 |
rs11042867 | snp | A/G | 0 | 0 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512934 | ACTTTTATATAGTGG[A/G]GTATAGGGTATGTGT | 50862 |
rs11042868 | snp | A/C | 0.305436 | 0.243776 | intron-variant | RNF141 | GRCh38.p7 | 11:10516781 | CTCTAAAGGGTCTTG[A/C]TATTAGTGGGACATA | 50862 |
rs11042869 | snp | G/T | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10518227 | ATACCATATGATCTA[G/T]CCATTCCATGTCTAG | 50862 |
rs11042870 | snp | C/T | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10525103 | AAAAGATTTAAGATG[C/T]TACAATGAGCAACAG | 50862 |
rs11042871 | snp | A/G | 0.416055 | 0.186885 | intron-variant | RNF141 | GRCh38.p7 | 11:10531204 | ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA | 50862 |
rs11042872 | snp | C/T | 0.415235 | 0.18761 | intron-variant | RNF141 | GRCh38.p7 | 11:10531243 | AGCCGGGCGTGGTGG[C/T]GTACACCTGTAATCC | 50862 |
rs11042873 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10535616 | GCTGAATTTCAAAGA[A/C]TAGTAAAATCTCAAA | 50862 |
rs11300664 | in-del | -/T | 0.499053 | 0.0217445 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513688 | CTCTATTTTCTTGTG[-/T]TTTTTTTTTGATTAG | 50862 |
rs11397587 | in-del | -/A/AT | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533540 | ACACAGTAAAAAAAA[-/A/AT]GTATATATATATATG | 50862 |
rs11553579 | snp | A/G | 0.0205511 | 0.0992634 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512250 | CATTTCATCCATTAA[A/G]CAAATTTACAACTTT | 50862 |
rs11602469 | snp | C/T | 0.24019 | 0.249807 | intron-variant | RNF141 | GRCh38.p7 | 11:10517269 | taatggcaagttaga[C/T]attgaagaaaaatgg | 50862 |
rs11604691 | snp | C/T | 0.242488 | 0.249887 | intron-variant | RNF141 | GRCh38.p7 | 11:10526501 | CAAGAATGAGTCATG[C/T]GGCCAGGCACGGTGG | 50862 |
rs11607008 | snp | C/G | 0.36606 | 0.221428 | intron-variant | RNF141 | GRCh38.p7 | 11:10517559 | aaaaactactctaag[C/G]cacatcataatcaaa | 50862 |
rs12099382 | snp | A/T | 0.0832709 | 0.186283 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511375 | ctaactaatgcctga[A/T]gatctgaggtggaaa | 50862 |
rs12225339 | snp | C/G | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10516489 | tgagctgaacacaca[C/G]agctgagaatcttgg | 50862 |
rs12225816 | snp | A/G | 0 | 0 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542119 | gcaatcctgtgagta[A/G]gtattattaatacct | 50862 |
rs12275930 | snp | C/T | 0.365232 | 0.22186 | intron-variant | RNF141 | GRCh38.p7 | 11:10531155 | GCCAAGGCAGGCAGA[C/T]CACGAGGTCAGGAGT | 50862 |
rs12277871 | snp | C/G | 0.497473 | 0.0354532 | intron-variant | RNF141 | GRCh38.p7 | 11:10534714 | GGTGATTTATCTAAA[C/G]TTACACAGCTGTAAG | 50862 |
rs12278433 | snp | C/T | 0.2776 | 0.248472 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542276 | actgCCTCGGTAGTA[C/T]GGTAAGACTTCATTA | 50862 |
rs12279850 | snp | C/T | 0.497695 | 0.0338674 | intron-variant | RNF141 | GRCh38.p7 | 11:10518383 | ACAAGCTATGGTATC[C/T]ACATAACAGACATTA | 50862 |
rs12290357 | snp | A/G | 0.366473 | 0.221211 | intron-variant | RNF141 | GRCh38.p7 | 11:10516623 | tgctgatcagtgtgt[A/G]catgtgaagacacta | 50862 |
rs12293993 | snp | C/T | | | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511378 | actaatgcctgatga[C/T]ctgaggtggaaaaat | 50862 |
rs12294022 | snp | C/G | 0.365232 | 0.22186 | intron-variant | RNF141 | GRCh38.p7 | 11:10531186 | TCGAGTCCAGCCTGA[C/G]CAACATGGTGAAACC | 50862 |
rs12575255 | snp | C/G | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542347 | ACAGCCAGCATGGTA[C/G]TTGTTCAATATTTGA | 50862 |
rs12789639 | snp | G/T | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10516063 | CAAAGTAATTATTTG[G/T]ATCAACTGCTCTTTG | 50862 |
rs12798409 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518179 | actgctttggaaaat[A/C]gctggcagcttttta | 50862 |
rs12798585 | snp | A/G | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10518256 | aggtattcacccaag[A/G]aaaaaaccaaaatac | 50862 |
rs12798593 | snp | A/C | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10518265 | cccaagaaaaaaacc[A/C]aaatacatccataaa | 50862 |
rs12799542 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10527193 | ctctaggcactagcc[A/C]cagtgtgtataaaac | 50862 |
rs16907941 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNF141 | GRCh38.p7 | 11:10521971 | GAACTCCAACTGATA[C/T]GGTACTTCAGGAAGA | 50862 |
rs16907951 | snp | C/G | 0.030278 | 0.119257 | intron-variant | RNF141 | GRCh38.p7 | 11:10531947 | CGGAGATCACTGCAC[C/G]TCTGAAATGCCAATT | 50862 |
rs16907954 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RNF141 | GRCh38.p7 | 11:10532983 | AAAAGGTCCAATCCT[C/T]AGCAGAGGGCCTTGC | 50862 |
rs16907957 | snp | C/G | 0.0325976 | 0.123435 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541430 | TGGCCATGGAAACAG[C/G]CTGGCAGACTCCCAT | 50862 |
rs16907959 | snp | A/C | 0.097727 | 0.198275 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541515 | GCCGCACTGAGAGCC[A/C]TGGTTTGGTCAACAG | 50862 |
rs17403175 | snp | A/C | 0.131038 | 0.219882 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540410 | ATCCACATTTTGTAA[A/C]GCCGAGACAAATAAC | 50862 |
rs34086731 | in-del | -/C | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513925 | AAATGATCCACCCAC[-/C]TCGGCCTCCCAAAGT | 50862 |
rs34252183 | in-del | -/C | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512093 | TGTTACTGAGTTAGG[-/C]ATAGGGAAAACAAAT | 50862 |
rs34271797 | in-del | -/A | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10535464 | AGGAAGATCCAGGCC[-/A]AAAAAAAAAAAAAAA | 50862 |
rs34466373 | snp | C/G | 0.468349 | 0.121752 | intron-variant | RNF141 | GRCh38.p7 | 11:10524217 | TTGGGAAATGGAGAC[C/G]GTCCTGGCTAACACG | 50862 |
rs34477334 | in-del | -/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520133 | TACAGTAGTGTACAG[-/C]ACTTTATGAACACTG | 50862 |
rs34553542 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | RNF141 | GRCh38.p7 | 11:10533160 | TGCTAGAGGCAGATT[C/T]AAAAGAAAGATATGA | 50862 |
rs34969789 | in-del | -/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10517926 | CATAAATTGAAATTT[-/T]AAATACCATTTAAAA | 50862 |
rs35065988 | in-del | -/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10521951 | TGTATAATCAAGGGG[-/G]AAGTGAACTCCAACT | 50862 |
rs35216368 | in-del | -/AA | 0.478271 | 0.101943 | intron-variant | RNF141 | GRCh38.p7 | 11:10535464 | AGGAAGATCCAGGCC[-/AA]AAAAAAAAAAAAAAA | 50862 |
rs35225578 | in-del | -/AT | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533542 | AGTATATATATATAT[-/AT]GCATGTGTGTGTCTA | 50862 |
rs35239960 | in-del | -/A | 0.383053 | 0.211653 | intron-variant | RNF141 | GRCh38.p7 | 11:10523746 | GAAGACTGTAACAAG[-/A]AAAAAACAATACTTT | 50862 |
rs35361495 | in-del | -/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520722 | GAGCAGCACAGTAGG[-/T]TTTGTTTACACCAGC | 50862 |
rs35522358 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539583 | ATCAACTTTTTTTTT[-/T]CAAGACAAGTTAATA | 50862 |
rs35663883 | in-del | -/AA | 0.497668 | 0.0340657 | intron-variant | RNF141 | GRCh38.p7 | 11:10518865 | ATAAATGTTAGGTGT[-/AA]AAACAAAAATAGTTT | 50862 |
rs35739697 | in-del | -/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10535937 | GTTACAGGACTTTTT[-/T]AAAATTAAATTCAAC | 50862 |
rs35925857 | in-del | -/AC | 0.42887 | 0.174658 | intron-variant | RNF141 | GRCh38.p7 | 11:10534478 | CACATGTGCATGTGT[-/AC]ACACACACACACACA | 50862 |
rs35958938 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10526475 | AGGCAGGGAAAAAAA[-/A]TACTGAGACTCAAGA | 50862 |
rs55642894 | in-del | -/G | 0.496968 | 0.0388195 | intron-variant | RNF141 | GRCh38.p7 | 11:10529052 | GCAGAAATAAAAGGT[-/G]TGGCAGAAACTACTG | 50862 |
rs55738534 | in-del | -/A | 0.257764 | 0.266729 | intron-variant | RNF141 | GRCh38.p7 | 11:10525081 | ACAATACCAACTGAG[-/A]AAAAAAAAAAGATTT | 50862 |
rs55785645 | in-del | -/G | 0.392918 | 0.20512 | intron-variant | RNF141 | GRCh38.p7 | 11:10527646 | TGCATGAGAAGTCAC[-/G]GGGGGGGGTTTTGAG | 50862 |
rs55965301 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539691 | AGAAAAAGATACATA[C/T]ATATATATTAGAGAG | 50862 |
rs56171160 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | RNF141 | GRCh38.p7 | 11:10534251 | ATATTATACAAAAAC[A/G]GCAATATACTCATTC | 50862 |
rs56298076 | in-del | -/A/ATATATATATATATATATAT/ATATATATATATATATATATATATATATATATATATATA | 0 | 0 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539699 | TACATACATATATAT[lengthTooLong]TAGAGAGAGAAGGAG | 50862 |
rs56724376 | snp | A/G | 0.0383715 | 0.133092 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512154 | TCCTAGAAGGCACAC[A/G]TTATATTTCCTATCA | 50862 |
rs56785085 | snp | A/C | 0.123452 | 0.215605 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513008 | AAGTTTTTGCTGCTG[A/C]AATAGTGTGAAAACC | 50862 |
rs56869832 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10536905 | AATGGTTAGGCCACA[C/T]TGAAAAGTCTGTATT | 50862 |
rs56886232 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10536746 | GGATTACAGGCATGA[A/G]CTGCCGCACCCGGCC | 50862 |
rs58146602 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533212 | GGGAGAAAATAAATA[G/T]CAAAAAAGTCATATT | 50862 |
rs58312518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528351 | ATAAAAAAATTTCTT[C/T]AGAGTAGCTCTAAAA | 50862 |
rs60120487 | in-del | -/AAAC/AC | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10532538 | CACACACACACACAC[-/AAAC/AC]CCCACAACTATATAC | 50862 |
rs60264919 | in-del | -/AAA | 0 | 0 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542806 | AAAAAAAAAAAAAAA[-/AAA]GCAGCAAATTTGGGA | 50862 |
rs60297712 | in-del | -/A | 0.461312 | 0.133593 | intron-variant | RNF141 | GRCh38.p7 | 11:10535357 | AATTTAAAAAAAAAA[-/A]CAAAAAACAACAGTT | 50862 |
rs61056815 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | RNF141 | GRCh38.p7 | 11:10523275 | TGTGCAAGATCTTTA[C/T]GCACCATAAAGTAAT | 50862 |
rs61176581 | snp | A/T | 0.426508 | 0.177045 | intron-variant | RNF141 | GRCh38.p7 | 11:10535357 | AGGACAATTGTAATT[A/T]AAAAAAAAAACAAAA | 50862 |
rs61564919 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542911 | GAATCAACCCAGGTG[C/T]TTATCAATAGTGGAT | 50862 |
rs61751345 | snp | C/T | 0.00214002 | 0.0326409 | missense | RNF141 | GRCh38.p7 | 11:10530666 | AGACCACCCGTACAA[C/T]CACTTTCCAAAAAGC | 50862 |
rs61760882 | snp | C/T | 0.00517778 | 0.050617 | missense | RNF141 | GRCh38.p7 | 11:10525304 | GACTTGTGATATCTT[C/T]ATAAAGTTGAATAAA | 50862 |
rs61891443 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF141 | GRCh38.p7 | 11:10515374 | ACTAGTATGTATCAG[C/T]ACCTGTTAGAGCTGT | 50862 |
rs61891444 | snp | G/T | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10529052 | GCAGAAATAAAAGGT[G/T]TGGCAGAAACTACTG | 50862 |
rs66565702 | in-del | -/TA | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539700 | TACATACATATATAT[-/TA]GAGAGAGAAGGAGAG | 50862 |
rs71476875 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF141 | GRCh38.p7 | 11:10524242 | AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT | 50862 |
rs71476876 | snp | C/T | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10529090 | ATCCAAATACCATTC[C/T]TTCTTTTCATTGCCA | 50862 |
rs72252394 | in-del | -/TA | 0.464794 | 0.159783 | intron-variant | RNF141 | GRCh38.p7 | 11:10533541 | CACAGTAAAAAAAAG[-/TA]TATATATATATATGC | 50862 |
rs72286083 | in-del | -/ACACACACAC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532497 | TTTAGTTCATTTTCT[-/ACACACACAC]ACACACACACACACA | 50862 |
rs72859152 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | RNF141 | GRCh38.p7 | 11:10518075 | TGTGGATAGGAAGAT[A/G]CACTAGTAAGAAATT | 50862 |
rs72859162 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RNF141 | GRCh38.p7 | 11:10518825 | AAAAGAAAAGTGTCA[A/G]AACTAAGGTACACCC | 50862 |
rs72859180 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF141 | GRCh38.p7 | 11:10533544 | CAGTAAAAAAAAGTA[C/T]ATATATATATGCATG | 50862 |
rs72859181 | snp | C/G | 0.0276057 | 0.114196 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10534039 | AAGCTCAGCTACTCT[C/G]CCAAGAAATTCTTCA | 50862 |
rs72859188 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | RNF141 | GRCh38.p7 | 11:10534974 | CTGCCTGGAAAAAGA[C/T]AGCTCTTTTGTTCAT | 50862 |
rs72859201 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | RNF141 | GRCh38.p7 | 11:10538900 | AGTGGTATTGCATAG[A/C]AACATAATTTGCAAA | 50862 |
rs73411920 | snp | G/T | 0.365853 | 0.221536 | intron-variant | RNF141 | GRCh38.p7 | 11:10516034 | TCTTTTCATCTCTCA[G/T]TGAAATCTGGGACCA | 50862 |
rs73411967 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | RNF141 | GRCh38.p7 | 11:10537008 | GTTTATTCTAGATAG[A/T]CATAGTTTGGTAACA | 50862 |
rs74555560 | snp | A/G | 0.0437281 | 0.141251 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511329 | GAACTGCGCATACGA[A/G]GGATCTAGGTTGCAT | 50862 |
rs74668259 | snp | C/T | 0.127599 | 0.217986 | intron-variant | RNF141 | GRCh38.p7 | 11:10520079 | CCCGTGGGCCGTGAG[C/T]TGAACAAGCTTGGCC | 50862 |
rs75074749 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF141 | GRCh38.p7 | 11:10537886 | CTTCCTCCTGGCATA[A/G]AGAGGACATCTTTCA | 50862 |
rs75146406 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | RNF141 | GRCh38.p7 | 11:10538362 | ATTGATAAATATTAA[C/T]ATCTATCACTATATG | 50862 |
rs75317269 | snp | C/T | 0.0481442 | 0.147493 | intron-variant | RNF141 | GRCh38.p7 | 11:10525176 | AAGTGAAATACAATA[C/T]TTATGCATTATATAC | 50862 |
rs75466849 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | RNF141 | GRCh38.p7 | 11:10524604 | AGAAGTGGGAACTTT[C/G]ATGTGCCAAAAGCAT | 50862 |
rs75559936 | snp | G/T | 0.00636936 | 0.0560724 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513698 | TTGTGTTTTTTTTTT[G/T]ATTAGGAGTCTCGTT | 50862 |
rs75606450 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | RNF141 | GRCh38.p7 | 11:10535710 | ATTCCCCAAAACTTA[A/G]CAAAAATCTCAAAAA | 50862 |
rs75741643 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF141 | GRCh38.p7 | 11:10528874 | GCTTACTCTCTAAAG[A/G]GGAGCTAAGAACCTA | 50862 |
rs75767167 | snp | C/G | 0.0372196 | 0.131242 | intron-variant | RNF141 | GRCh38.p7 | 11:10529077 | CTACTGGCTGATTAT[C/G]CAAATACCATTCCTT | 50862 |
rs75843556 | snp | C/T | 0.242488 | 0.249887 | intron-variant | RNF141 | GRCh38.p7 | 11:10526129 | ATGAAGAACTTGAAA[C/T]CAGAGAAAGATTAGA | 50862 |
rs75892811 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | RNF141 | GRCh38.p7 | 11:10536439 | GCCTGCCCAATCTGC[A/G]GATGACCAAAACTGG | 50862 |
rs75984337 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10535337 | TAGTTACCTAAAATA[G/T]GAAAAGGACAATTGT | 50862 |
rs75984521 | snp | A/G | 0.121022 | 0.21416 | intron-variant | RNF141 | GRCh38.p7 | 11:10528113 | AGATCATTTTTTATA[A/G]TGGATTAAATATTAT | 50862 |
rs75985942 | snp | C/T | 0.127254 | 0.217792 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539485 | CATCAGTAATAAATA[C/T]CAAGTACTACTGACT | 50862 |
rs76344980 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | RNF141 | GRCh38.p7 | 11:10523027 | ATAGGAAAAACTTCA[C/T]AGTGATTAGAGCCAT | 50862 |
rs76359767 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | RNF141 | GRCh38.p7 | 11:10531863 | TGAAAATAATTCAGC[C/T]GTGCCAGTTTCCAGC | 50862 |
rs76511572 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | RNF141 | GRCh38.p7 | 11:10520945 | CTAAAATATGGATCC[G/T]GCCATCAGGGCCTTA | 50862 |
rs76543455 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | RNF141 | GRCh38.p7 | 11:10522193 | AACTGAATAAAAACC[C/T]AGATGGATATGGGTC | 50862 |
rs76944040 | snp | A/C | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10526784 | AAGACTACGTCTCAA[A/C]AAAAAAAAAAAAGAA | 50862 |
rs76949881 | snp | C/T | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10533636 | TTACCTTTGACTATC[C/T]TAGGAGTCTTTCTCT | 50862 |
rs76997837 | snp | C/T | 0.0298908 | 0.118541 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513474 | TTACATGCCGAAATG[C/T]TAATGTTAGAAATTT | 50862 |
rs77182231 | snp | A/T | 0.0158469 | 0.0875917 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10543153 | ACTGGGGATTCCAAA[A/T]GGGTAGAAAAAACTA | 50862 |
rs77232267 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | RNF141 | GRCh38.p7 | 11:10529523 | AGCAAAAGAAGGTCA[C/T]TGTGACTAATGCAGA | 50862 |
rs77238187 | snp | A/G | 0.0433465 | 0.140692 | intron-variant | RNF141 | GRCh38.p7 | 11:10522944 | ATTTGAACACAGGCA[A/G]CTTGCTGCTAGAGTC | 50862 |
rs77318898 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RNF141 | GRCh38.p7 | 11:10518620 | ATAAATTATCCTAAA[C/T]GCTCAAGTCTTATTT | 50862 |
rs77408036 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518868 | AATGTTAGGTGTAAA[A/C]ACAAAAATAGTTTTA | 50862 |
rs77540212 | snp | A/G | 0.021333 | 0.101051 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513298 | GAATTTTATTTGCTC[A/G]CCTATTAAAATCCTA | 50862 |
rs77642769 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | RNF141 | GRCh38.p7 | 11:10535812 | AATGAGGTATACCAC[A/G]TATTTACCAGGTATA | 50862 |
rs78042849 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNF141 | GRCh38.p7 | 11:10520976 | CAATGCTGACATTGA[C/T]AATGGGCATATGAGT | 50862 |
rs78103080 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RNF141 | GRCh38.p7 | 11:10539072 | TTTCTAAATAAAGAA[C/T]TGTTATTTTGAAATG | 50862 |
rs78195437 | snp | G/T | 0.5 | 0 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513697 | CTTGTGTTTTTTTTT[G/T]GATTAGGAGTCTCGT | 50862 |
rs78208556 | snp | A/T | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10535479 | AAAAAAAAAAAAAAA[A/T]ATCCCTGAAGTCAAA | 50862 |
rs78222409 | snp | C/T | 0.0444908 | 0.142359 | intron-variant | RNF141 | GRCh38.p7 | 11:10518870 | TGTTAGGTGTAAAAA[C/T]AAAAATAGTTTTAAC | 50862 |
rs78422509 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | RNF141 | GRCh38.p7 | 11:10533380 | AAGGCAGAGAAATTT[A/G]TATTTCATTTTAGAA | 50862 |
rs78443895 | snp | A/G | 0.0314385 | 0.121371 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542839 | ACAAATTTGACCAAA[A/G]ATGAGAAAGACATGT | 50862 |
rs78454694 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10529967 | TCTTTATGGGTCAGT[C/T]GGGAATGAACTTCAG | 50862 |
rs78459807 | snp | A/T | 0.449473 | 0.150701 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539700 | TACATACATATATAT[A/T]AGAGAGAGAAGGAGA | 50862 |
rs78611131 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF141 | GRCh38.p7 | 11:10529956 | AACCCAGGGAATCTT[C/T]ATGGGTCAGTCGGGA | 50862 |
rs78627715 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10529668 | TAATCTCACAGCAGC[A/G]TAAATTAGAATTTGG | 50862 |
rs78631641 | snp | A/G | 0.0189856 | 0.0955633 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511321 | TCTACTGTGAACTGC[A/G]CATACGAGGGATCTA | 50862 |
rs78662548 | snp | A/T | 0.449473 | 0.150701 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539701 | ACATACATATATATT[A/T]GAGAGAGAAGGAGAG | 50862 |
rs78823513 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10518306 | CATGAATGTATCTAG[C/T]ACCTTTATTTTGTAA | 50862 |
rs79381197 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | RNF141 | GRCh38.p7 | 11:10536880 | AGCCTACTAGTCCAT[C/T]ATGCTTTGCAATGGT | 50862 |
rs79433429 | snp | C/T | 0.126564 | 0.217402 | intron-variant | RNF141 | GRCh38.p7 | 11:10527854 | ATAGGGTGGTAGTAG[C/T]GTAGATGGTGAGAGC | 50862 |
rs79453359 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | RNF141 | GRCh38.p7 | 11:10533399 | TTCATTTTAGAAATT[C/T]AGTCAAAGAGTTAAG | 50862 |
rs79627155 | snp | G/T | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10534409 | CTTATATATTATTGG[G/T]AGGGTGATGAACCTC | 50862 |
rs79676535 | snp | A/C | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10526782 | GCAAGACTACGTCTC[A/C]AAAAAAAAAAAAAAG | 50862 |
rs79708961 | snp | A/C/T | 0.0807149 | 0.183963 | intron-variant | RNF141 | GRCh38.p7 | 11:10531821 | ATCGAAAGTTAAGCA[A/C/T]CTAGCCTTAGGAAAC | 50862 |
rs79837439 | snp | A/G | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10543071 | AGGAAACCAAATACC[A/G]CATGTTCTCACTTAT | 50862 |
rs79843915 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | RNF141 | GRCh38.p7 | 11:10534433 | GAACCTCTAATTCTT[A/G]TAATTTTACCAAGTC | 50862 |
rs80211110 | snp | A/T | 0.0532157 | 0.154195 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541926 | TGCTGCCTCTATGCT[A/T]AGCAGTTAAACTGGT | 50862 |
rs80348845 | in-del | -/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10525090 | ACTGAGAAAAAAAAA[-/G]AGATTTAAGATGCTA | 50862 |
rs111313915 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10539012 | CCTATAACACAGTCA[G/T]TTTTTGCAAGATAAA | 50862 |
rs111390498 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541941 | TAGCAGTTAAACTGG[A/T]TTTTATGTTTCTTGT | 50862 |
rs112049768 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539483 | AACATCAGTAATAAA[C/T]ACCAAGTACTACTGA | 50862 |
rs112124363 | snp | C/T | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10516318 | TTTCATACAATCTTT[C/T]AAATAAAGCACTGGC | 50862 |
rs112772521 | snp | C/G | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10529240 | GAAGGGGATATGACC[C/G]AATACTGACCAGTGA | 50862 |
rs112980556 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | RNF141 | GRCh38.p7 | 11:10518378 | AATAAACAAGCTATG[A/G]TATCCACATAACAGA | 50862 |
rs113144253 | snp | C/T | | | splice-acceptor-variant | RNF141 | GRCh38.p7 | 11:10534207 | GCTTCACATAGTTTC[C/T]GTCAAATATACAGAA | 50862 |
rs113251963 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10521237 | CTCAGCTCAAAACAT[C/T]ATCATCTCTCTGCTC | 50862 |
rs113389401 | in-del | -/A | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10524405 | GACTCCGCCTCAATT[-/A]AAAAAAAAAAAATCA | 50862 |
rs113547060 | snp | C/T | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10532696 | AGACAGTATATCAAG[C/T]TTATCTAATATGTTA | 50862 |
rs113669759 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | RNF141 | GRCh38.p7 | 11:10517854 | GAGTTTAATAAGGGC[A/G]CAGGATACAAGGTTG | 50862 |
rs113713723 | snp | A/G | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10531846 | GGAAACAAAGTCTTC[A/G]GTGAAAATAATTCAG | 50862 |
rs113855738 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518869 | ATGTTAGGTGTAAAA[A/C]CAAAAATAGTTTTAA | 50862 |
rs113869643 | snp | C/G | | | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541251 | AAAGCCCCGCCCCCC[C/G]CGCGTTGCCGGGAGA | 50862 |
rs114015865 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | RNF141 | GRCh38.p7 | 11:10521098 | CTTGGGAAGAAAAAA[C/G]ATTTCAAACCTTTTG | 50862 |
rs114016937 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540888 | AGGCGGGACAAGCCA[A/C]CGCCACCCCGGGCAA | 50862 |
rs114047722 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | RNF141 | GRCh38.p7 | 11:10516861 | AGCAAGATCCAAAAG[A/G]ATCAAACTGTTTCCA | 50862 |
rs114073990 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10524458 | TAAGGTAAAGGACAC[A/G]GTGAATATAGATTTC | 50862 |
rs114139819 | snp | A/C | 0.0185938 | 0.0946107 | intron-variant | RNF141 | GRCh38.p7 | 11:10520797 | ATGGCTACGACGTCC[A/C]CAGGCAATAGGAATT | 50862 |
rs114283233 | snp | A/C | 0.021333 | 0.101051 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514139 | CCTTCTGAAACTCCA[A/C]GATGTGTGAGCATTA | 50862 |
rs114293149 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | RNF141 | GRCh38.p7 | 11:10525503 | TTTGCAAATTACATA[A/T]GAAAGCAAGAGTCTG | 50862 |
rs114327186 | snp | A/G | 0.0310518 | 0.120672 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541897 | AAGGATTTTAACCCA[A/G]GTACAGCTGACACTG | 50862 |
rs114559264 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF141 | GRCh38.p7 | 11:10524126 | CAGTAAAAAAAAAGA[A/G]ACCACTGGCCGGGCA | 50862 |
rs114737392 | snp | G/T | 0.123452 | 0.215605 | intron-variant | RNF141 | GRCh38.p7 | 11:10527652 | AGAAGTCACGGGGGG[G/T]GGTTTTGAGCCAAGG | 50862 |
rs115378378 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | RNF141 | GRCh38.p7 | 11:10527828 | CTGGTGATAGAGGAT[A/G]GTCACTAGGAATAGG | 50862 |
rs115416835 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | RNF141 | GRCh38.p7 | 11:10524108 | ATGCAACTGTAAATA[C/G]AGCAGTAAAAAAAAA | 50862 |
rs115483585 | snp | A/G | 0.031825 | 0.122064 | intron-variant | RNF141 | GRCh38.p7 | 11:10528556 | AGAGCAACAAAAAAC[A/G]AAGGGATGAAAAGCC | 50862 |
rs115774430 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | RNF141 | GRCh38.p7 | 11:10522325 | ACAAAGAAGAGCATT[A/G]TGGAGAGAGATAAAA | 50862 |
rs115891698 | snp | C/G | 0.0349115 | 0.127424 | intron-variant | RNF141 | GRCh38.p7 | 11:10521260 | CTCTGCTCTCAAAAT[C/G]AACACTTGCCTCAAT | 50862 |
rs116019146 | snp | C/T | 0.0298908 | 0.118541 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541780 | AGTAATTGCTGTCTT[C/T]TAAGCATCTGTTGTG | 50862 |
rs116076998 | snp | C/G | 0.0433465 | 0.140692 | intron-variant | RNF141 | GRCh38.p7 | 11:10523635 | AACTGAAAAAACACA[C/G]AAAAACAAGAAGCAC | 50862 |
rs116163993 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10520392 | AACTAAGACATAACA[C/T]ACACATTAGCCTAGG | 50862 |
rs116229896 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10532764 | GGTTGTAATGCCTAC[A/G]GAGTGGGTTCATATA | 50862 |
rs116254462 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF141 | GRCh38.p7 | 11:10515749 | CTACATGACTTTCAA[C/T]AATATATCTACCTGT | 50862 |
rs116351595 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | RNF141 | GRCh38.p7 | 11:10523637 | CTGAAAAAACACACA[A/G]AAACAAGAAGCACCC | 50862 |
rs116472878 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10516915 | AAAAAGCTCAAGAAT[A/T]TTCATAGGAATACAA | 50862 |
rs116474289 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | RNF141 | GRCh38.p7 | 11:10521258 | CTCTCTGCTCTCAAA[A/C]TCAACACTTGCCTCA | 50862 |
rs116601223 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516818 | TCTAAACTAAATACT[G/T]CTCTGGTCCTGCCTA | 50862 |
rs116660411 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | RNF141 | GRCh38.p7 | 11:10520491 | TCAGGGGCAGTAACA[G/T]GCACGGAGCTGTCAT | 50862 |
rs116856219 | snp | G/T | 0.0252325 | 0.109451 | intron-variant | RNF141 | GRCh38.p7 | 11:10527960 | CAAGAATGACTCTAA[G/T]AAGTTGGTCTAAGAA | 50862 |
rs116886144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536397 | TTGGGCTGTTTAACA[C/T]TTTTGTTGATGACCT | 50862 |
rs116933651 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | RNF141 | GRCh38.p7 | 11:10538536 | TATTTCTATCATACT[A/G]TGACATTCGTTAAGT | 50862 |
rs116948854 | snp | C/T | 0.0130921 | 0.0798413 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10543080 | AATACCGCATGTTCT[C/T]ACTTATAAGTAGGAG | 50862 |
rs117013174 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520067 | GGCTGCATGCAGCCC[A/G]TGGGCCGTGAGTTGA | 50862 |
rs117022703 | snp | A/G | 0.0189856 | 0.0955633 | utr-variant-5-prime, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541133 | TCACCCCAGGTTCAA[A/G]GCATCGCGCACCCTG | 50862 |
rs117223295 | snp | C/T | 0.0726307 | 0.176182 | intron-variant | RNF141 | GRCh38.p7 | 11:10524180 | AGCACTCTGGGAGGC[C/T]GAGGAGGGCAGGATC | 50862 |
rs117417228 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF141 | GRCh38.p7 | 11:10529139 | TTTGTGTCCACCATT[C/G]CCTGAAATGATGCAG | 50862 |
rs117752844 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RNF141 | GRCh38.p7 | 11:10527785 | CAAGAGAAGCAGGGA[C/G]ATCAGTTAGGAGGCT | 50862 |
rs117826075 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | RNF141 | GRCh38.p7 | 11:10529417 | GAATGGACATCCTAG[C/T]TGAGAAAACACAATA | 50862 |
rs117917097 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | RNF141 | GRCh38.p7 | 11:10530501 | ACAGCTAGTTAGAAG[A/G]CAATAACAGTAACAA | 50862 |
rs137961212 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10529851 | ACTGGAAGCAAAACA[C/G]AGTATGGGTAAAACT | 50862 |
rs138141231 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514408 | AATAATTAACCACAA[A/G]GGGGCATATATATAT | 50862 |
rs138261501 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520118 | TACTGTATAGCACTT[A/G]TACAGTAGTGTACAG | 50862 |
rs138511396 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10533124 | TAGAAGATATACATA[A/G]ATAAAGGTAGATGTG | 50862 |
rs138553753 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10529383 | TTAACAGGAATTTTC[C/T]GTGACTTCCTAATGG | 50862 |
rs138561992 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541805 | GTTGTGTGCCAAATA[C/T]TGCACTAGGCACTTT | 50862 |
rs138606542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10536148 | AAGGGGGACTTGACC[C/T]AGTTTTGTATCAGGG | 50862 |
rs138840496 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10519509 | TTAAAGACAGAGATA[C/T]GGTCTGAGAAACTCA | 50862 |
rs138885503 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512537 | TATCCCTGGAAAGAT[C/G]CAAAACTCTGTAAGG | 50862 |
rs138886304 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10515317 | ACACACATGCACGCA[C/T]GTGCACACACACATT | 50862 |
rs138923608 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10525021 | CTTTAATTTAGCACT[A/G]TAACAACATCCGAAG | 50862 |
rs139011435 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517013 | CTACCAGACATACAA[A/G]AAAGCAGCAGAAAAA | 50862 |
rs139138527 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10523128 | AAGTCGGACTTGGCA[A/C]AATGTGGGTAAGCAG | 50862 |
rs139348520 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10537609 | AACAGGAGAAAAACA[C/G]ACAAATTTTATTTAG | 50862 |
rs139768305 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511208 | GTTAGGAACCAGGCC[A/G]CACAGCAGGAGTTGA | 50862 |
rs139905748 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNF141 | GRCh38.p7 | 11:10531125 | CTCACACCTGTAATC[C/T]CAGCACTTTGGGAGG | 50862 |
rs139939161 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | RNF141 | GRCh38.p7 | 11:10526599 | CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT | 50862 |
rs139943988 | snp | C/T | 0.00026421 | 0.0114906 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10519114 | CATACAGATACAACA[C/T]TCCTCCTCATCGGTC | 50862 |
rs140338852 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10522184 | GAATGGGAAAACTGA[A/G]TAAAAACCTAGATGG | 50862 |
rs140393944 | snp | A/C/G | 0.00136682 | 0.0261066 | missense | RNF141 | GRCh38.p7 | 11:10534085 | CTCTCTCGAACCAAC[A/C/G]TAACATGTTTTGCTA | 50862 |
rs140394458 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512841 | GGATATCACCAATGC[A/G]TTAATGTTTTTATTC | 50862 |
rs140916965 | snp | C/T | 1.65187e-05 | 0.00287386 | missense | RNF141 | GRCh38.p7 | 11:10519115 | ATACAGATACAACAC[C/T]CCTCCTCATCGGTCA | 50862 |
rs141068390 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539797 | TGTGTTTACTAAATG[C/T]ATTTCATATTGGAAA | 50862 |
rs141100668 | in-del | -/TTAA | 0.159292 | 0.232964 | intron-variant | RNF141 | GRCh38.p7 | 11:10533431 | AGAAATTTAAAGGTG[-/TTAA]TTAATTAGAAAATAT | 50862 |
rs141114989 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10524006 | CCAAGTAATTCTATT[A/C]AAGATAATTGGGAAA | 50862 |
rs141628297 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542016 | AAGAGCTAATTCTTC[A/C]CTCTAATAATAATAC | 50862 |
rs141697466 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF141 | GRCh38.p7 | 11:10536301 | AGACAGGAAGCAGCA[C/T]GGTGACTTTGAGGTA | 50862 |
rs141752749 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10543008 | TATCTTTTGCAGCAA[C/T]ATGAATACAGCTGGA | 50862 |
rs141780860 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10529196 | AACCAATCATGCTAA[C/T]CATATTCCCTCTGTC | 50862 |
rs141875097 | in-del | -/GCTCTG | 0.0437281 | 0.141251 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540714 | GCCACCCTAGCGCTC[-/GCTCTG]GCTCTGGCTACGCCG | 50862 |
rs141932259 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10524873 | TAAAAAGCTTTGACT[A/G]TCTAAGAACCTAAAT | 50862 |
rs142047533 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10519623 | GCTATATGGCATAGT[C/G]TATTGCTTCTAGGCT | 50862 |
rs142073895 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10518057 | GGAGAAATATACAGC[A/G]TATGTGGATAGGAAG | 50862 |
rs142139233 | snp | A/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512255 | CATCCATTAAACAAA[A/T]TTACAACTTTTACGA | 50862 |
rs142280499 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10538373 | TTAACATCTATCACT[A/C]TATGGGTGTGAAAAT | 50862 |
rs142553303 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512000 | ACACAGATCCTATTA[C/T]TCTCAACCTCTAAAT | 50862 |
rs142590682 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF141 | GRCh38.p7 | 11:10526212 | AAGTAAGCCATGAAA[C/T]CTATTAAGTGCATAT | 50862 |
rs142716810 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10525391 | AAAAATACAAAGAAC[A/G]TGAAAAAGAAAAGTT | 50862 |
rs142862260 | snp | A/G | 1.66905e-05 | 0.00288876 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10514925 | TCAAGGTCATGGCCT[A/G]TGGGGCTGGCCTGCC | 50862 |
rs142974980 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF141 | GRCh38.p7 | 11:10516641 | TGTGAAGACACTACC[A/G]AGGCTGAACAATCAA | 50862 |
rs143308426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10525033 | ACTGTAACAACATCC[A/G]AAGCACAGAATAACC | 50862 |
rs143311292 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF141 | GRCh38.p7 | 11:10528117 | CATTTTTTATAGTGG[A/G]TTAAATATTATTTAA | 50862 |
rs143372370 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | RNF141 | GRCh38.p7 | 11:10521568 | GTGCTTATAGCACTG[G/T]ATGTAAGATATTTAG | 50862 |
rs143413420 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10533366 | GTGTACTCTTTAAGA[A/G]GGCAGAGAAATTTAT | 50862 |
rs143477919 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | RNF141 | GRCh38.p7 | 11:10526655 | GAGCATGGTGGCACA[C/T]GCCTATAGTCCCAGC | 50862 |
rs143643622 | in-del | -/TT | 0.355954 | 0.226437 | intron-variant | RNF141 | GRCh38.p7 | 11:10520258 | TTAACTTTTTGACTC[-/TT]TTTGTAACAACACTT | 50862 |
rs143669337 | in-del | -/AT | 0.0410537 | 0.137264 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514413 | TAACCACAAGGGGGC[-/AT]ATATATATATATACT | 50862 |
rs143979854 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531052 | TCTAACAAAGACATT[C/T]AGGAAAAACAAGTCT | 50862 |
rs144173377 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10537961 | AGTGGGCACTTCTTA[A/C/T]ATCTGCTGCTTTTCA | 50862 |
rs144303403 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10522619 | TCCTTGAGAACAGAA[A/G]GTTCAGTGAGAATTT | 50862 |
rs144373379 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF141 | GRCh38.p7 | 11:10520615 | ACTCTAAAATGATTA[A/G]AAAGTATAGTATAGT | 50862 |
rs144477174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10525648 | GATGGGTAAGGTGAC[C/T]TTCTCAGAGTTAAGA | 50862 |
rs144607848 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541598 | ATACACAAAGGTCAT[A/C]TTGTTTCTTTATGAG | 50862 |
rs144643991 | in-del | -/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10528476 | CACATACAGATGTTA[-/G]ACATATTGAGGCAAA | 50862 |
rs144806814 | in-del | -/AT | 0.00676609 | 0.0577691 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542028 | TTCCCTCTAATAATA[-/AT]ACTCTTTGACCATTT | 50862 |
rs144898917 | snp | A/G | 4.94336e-05 | 0.00497135 | stop-gained | RNF141 | GRCh38.p7 | 11:10534077 | AGGAGCCACTCTCTC[A/G]AACCAACGTAACATG | 50862 |
rs145008358 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519312 | TTTAGGGATAGCAAA[C/T]ATATTAGGGAAAAAG | 50862 |
rs145062180 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | RNF141 | GRCh38.p7 | 11:10523406 | GGCTGAAATGGGCCG[A/G]TAATTGTACTCCCAT | 50862 |
rs145223530 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10527196 | TAGGCACTAGCCACA[A/G]TGTGTATAAAACAAA | 50862 |
rs145397122 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542018 | GAGCTAATTCTTCCC[C/T]CTAATAATAATACTC | 50862 |
rs145731752 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | RNF141 | GRCh38.p7 | 11:10519849 | GTCAGTGAGTGAGTA[A/G]TGGTGAGTGGATATG | 50862 |
rs145882090 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540608 | TAAGTGTGGGGCTGG[A/C]TAAGTAGATCGACGT | 50862 |
rs145986631 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512262 | TAAACAAATTTACAA[A/C]TTTTACGATTAGTTA | 50862 |
rs146085326 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515164 | CTTTTAAAAAGGAAA[A/C/T]AGCATAGAAATATAT | 50862 |
rs146235332 | snp | A/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10516924 | AAGAATATTCATAGG[A/T]ATACAAAAATATCCA | 50862 |
rs146246449 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF141 | GRCh38.p7 | 11:10537016 | TAGATAGTCATAGTT[C/T]GGTAACAATGAAGCA | 50862 |
rs146265130 | snp | A/T | 0.0429648 | 0.14013 | intron-variant | RNF141 | GRCh38.p7 | 11:10531176 | GGTCAGGAGTTCGAG[A/T]CCAGCCTGACCAACA | 50862 |
rs146767198 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | RNF141 | GRCh38.p7 | 11:10526832 | TAAGAAATTTTAGAA[C/T]CATCTCTAATAATCA | 50862 |
rs147110217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10529208 | TAATCATATTCCCTC[C/T]GTCAGTGTAGGTGTA | 50862 |
rs147142952 | snp | A/T | 0.0205511 | 0.0992634 | intron-variant | RNF141 | GRCh38.p7 | 11:10522135 | TTAAGTGTTATACGT[A/T]AGTAACAGGGAAAAG | 50862 |
rs147416594 | in-del | -/TTAT | 0.0197687 | 0.0974348 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511947 | ATCACTTGCGAAAGA[-/TTAT]TTATTGCACAATTTA | 50862 |
rs147548510 | snp | A/T | 0.000329592 | 0.0128331 | missense | RNF141 | GRCh38.p7 | 11:10525242 | AGAGGATGAGTTTTC[A/T]TCAGGTTCTTCAGAG | 50862 |
rs147595481 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512022 | CCTCTAAATTCAGTA[A/C]ATAGTAAAATTCATT | 50862 |
rs147716595 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539658 | AGAATGCCTGTTCCA[C/G]AATCAAAGATCTTGA | 50862 |
rs147796725 | in-del | -/TT | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531567 | AATGATTTGAGACAC[-/TT]TATATATAGCTCTAC | 50862 |
rs147823232 | snp | A/C | 0.0142736 | 0.0832652 | intron-variant | RNF141 | GRCh38.p7 | 11:10518516 | TATATGATTCCATTT[A/C]TAAAAATTCATAACT | 50862 |
rs147895815 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538754 | ACTAGGTTGGAGAGA[A/G]GCAGAAGTTAAAAAT | 50862 |
rs147912658 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10531486 | CAGTCCTTGTTCAAA[C/T]AATGATACTAACAAA | 50862 |
rs148028642 | snp | A/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542954 | GTGTGGTACATATAC[A/G]CCATGGAATACTATA | 50862 |
rs148118372 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10524376 | GCCGAGATCGCGCCT[A/G]GGCGACAGAGCAAGA | 50862 |
rs148350291 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528656 | TGAAATAAAAATGAA[A/C]ATTAAGTGTAATTTA | 50862 |
rs148434632 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526176 | TTTCAGCACAAGACA[C/T]AGGATGGAAGACTGG | 50862 |
rs148574442 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515468 | GGACATTTAGTTTTT[C/T]TTCCCATCTTTTGTT | 50862 |
rs148713158 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | RNF141 | GRCh38.p7 | 11:10538271 | AGAGACTACCTGAGA[C/G]AGCCTGCAGAAGTGG | 50862 |
rs148736029 | in-del | -/GT | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512230 | TACAGAATACAAAAA[-/GT]GTACATTTCATCCAT | 50862 |
rs148834059 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511859 | AATATAAAATAGTTC[C/T]CTAAGGAATATAAAC | 50862 |
rs148887529 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | RNF141 | GRCh38.p7 | 11:10518595 | ACATGTAGTTTATTG[C/T]ATGTATTTTATAAAT | 50862 |
rs149026546 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540641 | CTATTTCTGAGCTAT[C/T]GTCCCAGGCAAAAGG | 50862 |
rs149167764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527264 | AGACAGGCAAATAAA[A/G]TACAGATACAGATTA | 50862 |
rs149560588 | in-del | -/A | 0.0138799 | 0.0821421 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514243 | ATCCATTTGCAAAGG[-/A]AAAGTCACACCCAAT | 50862 |
rs149571700 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514527 | TCTCTCAGATGGCTA[A/C]AACTTTTTAATATTC | 50862 |
rs149624246 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520128 | CACTTGTACAGTAGT[A/G]TACAGACTTTATGAA | 50862 |
rs149656586 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511233 | AGTTGAGCCGCGGGC[A/G]AGTGAGTATTATTGC | 50862 |
rs149689561 | in-del | -/CCA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532540 | ACACACACACACACC[-/CCA]CAACTATATACAGCT | 50862 |
rs149792857 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | RNF141 | GRCh38.p7 | 11:10531319 | GGTGAAGGTTGTAGT[A/G]AGCCAAGATCACGCC | 50862 |
rs149870408 | snp | A/C | 0.000153988 | 0.00877328 | stop-gained | RNF141 | GRCh38.p7 | 11:10534050 | CTCTCCCAAGAAATT[A/C]TTCATAAGTTAAGGA | 50862 |
rs149934936 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | RNF141 | GRCh38.p7 | 11:10523399 | ATTCTTTGGCTGAAA[C/T]GGGCCGATAATTGTA | 50862 |
rs149956918 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | RNF141 | GRCh38.p7 | 11:10537623 | ACACAAATTTTATTT[A/G]GTAATTTTTATACAT | 50862 |
rs149989723 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10527168 | GATGTTATTGGTACT[A/G]TGTGCACTGCTCTAG | 50862 |
rs150133913 | in-del | -/AAAA | | | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542788 | ATATCTCTTATCAGC[-/AAAA]AAAAAAAAAAAAAAA | 50862 |
rs150246483 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | RNF141 | GRCh38.p7 | 11:10525017 | GCCACTTTAATTTAG[C/T]ACTGTAACAACATCC | 50862 |
rs150264751 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540217 | GGGAGTGAAAACGAA[A/T]AAATTCGTGCTGAAG | 50862 |
rs150701030 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10516653 | ACCGAGGCTGAACAA[A/T]CAATCAAAGGGCTTT | 50862 |
rs150719420 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | RNF141 | GRCh38.p7 | 11:10529812 | ATGCCTCTCACACTT[A/G]TGCTCAAATGTTTAT | 50862 |
rs150985730 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | RNF141 | GRCh38.p7 | 11:10526384 | AGATTACATATTTTA[A/T]AATATTATTATACAT | 50862 |
rs151017703 | snp | A/G | 0.00178059 | 0.0297846 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10519087 | AGGCAGGATGAGGTC[A/G]GCCCGCCCATCCATA | 50862 |
rs151034435 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | RNF141 | GRCh38.p7 | 11:10531231 | AATACAAAAATTAGC[C/T]GGGCGTGGTGGCGTA | 50862 |
rs151176756 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | RNF141 | GRCh38.p7 | 11:10522694 | TTTGTTTGGAGGAAT[A/T]CCAGAGGGCACAGCC | 50862 |
rs180852871 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10533860 | AGCTACATAGAAAGT[C/T]AACTTATAATAGATA | 50862 |
rs180853083 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF141 | GRCh38.p7 | 11:10526640 | TACAAAAAATTAGCT[A/G]AGCATGGTGGCACAC | 50862 |
rs180961468 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | RNF141 | GRCh38.p7 | 11:10518091 | CACTAGTAAGAAATT[C/T]ACTCTCCCTAAATTG | 50862 |
rs181037415 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10529918 | TAACCTCCAGGGTCC[A/G]TGACTCAAAGGAAAA | 50862 |
rs181078215 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10534830 | ACATCAGCTAAATAA[C/T]TTTTTGTTGAATTAC | 50862 |
rs181088161 | snp | A/C | 0.127944 | 0.218179 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514244 | ATCCATTTGCAAAGG[A/C]AAGTCACACCCAATT | 50862 |
rs181201980 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520261 | ACTTTTTGACTCTTT[G/T]TGTAACAACACTTAC | 50862 |
rs181217129 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10530534 | CTATGTTTTACAAAA[C/T]CACCGAGTTATTAAA | 50862 |
rs181710479 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10526047 | GCTTTCACAAGCTTT[A/G]GGGAGCCATGGAGTG | 50862 |
rs181711647 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540343 | GTCAGAATATAAAAG[A/G]TACACTACCTTTAAT | 50862 |
rs181789562 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | RNF141 | GRCh38.p7 | 11:10518823 | GCAAAAGAAAAGTGT[C/T]AAAACTAAGGTACAC | 50862 |
rs181814803 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542385 | ATGAATATTTGAACA[C/T]TGGAAAAGGAAAAAG | 50862 |
rs181825755 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514777 | TTTTTAAAAGGGGGA[A/C]AAATGATCAGAATAG | 50862 |
rs181834411 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10520091 | GAGTTGAACAAGCTT[G/T]GCCTAGGACATTACT | 50862 |
rs181938919 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528957 | AATCTGGAAGAGACA[A/G]GAGAACTCCTATTCA | 50862 |
rs182118053 | snp | A/T | 0.031825 | 0.122064 | intron-variant | RNF141 | GRCh38.p7 | 11:10535937 | GTTACAGGACTTTTT[A/T]AAAATTAAATTCAAC | 50862 |
rs182403694 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10521776 | GGTAAAAAGCAAAAT[A/C]ATGTGTGTTTATGTC | 50862 |
rs182474882 | snp | C/T | 0.00199481 | 0.0315187 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511360 | GCACCTTATGAGAAT[C/T]TAACTAATGCCTGAT | 50862 |
rs182553878 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516133 | AATGTGAAAGCTACA[C/G]CTGGCATATATTATT | 50862 |
rs182563305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538152 | CCCTAACTTTGAGTA[A/C]AGTTTATAATTTGAG | 50862 |
rs182872076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527080 | TCAGTACAGAAATAG[C/T]AAAGTGTATCACACT | 50862 |
rs183007898 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10531847 | GAAACAAAGTCTTCG[A/G]TGAAAATAATTCAGC | 50862 |
rs183174893 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523283 | ATCTTTATGCACCAT[A/C]AAGTAATAGGTTAGA | 50862 |
rs183313690 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522094 | AAGAAGCATTATAAA[A/G]GACAAATCTTTTATG | 50862 |
rs183401903 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10515711 | GAAGAAAGGATATTA[C/T]TAATTATTTTTCTAA | 50862 |
rs183738338 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF141 | GRCh38.p7 | 11:10530904 | TAATAACTGGATTCT[C/T]AAAACAGGGATAGAG | 50862 |
rs183770811 | snp | G/T | 0.00478085 | 0.0486577 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513421 | TCAGAAAAGTTACAT[G/T]GAATGTTAAATTTTA | 50862 |
rs183886541 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10537089 | AACAAGATTCATTTA[C/T]AGAGAATGGGATGGC | 50862 |
rs183895294 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10518497 | AGACAAAAAAAGCAC[A/C]TATTATATGATTCCA | 50862 |
rs183921622 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539959 | AATGACAAATATTAA[C/T]TTTTGAAACATATAG | 50862 |
rs184093337 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10527913 | GACAGGACTCACTTA[C/T]AGATTGTCAGGTGTG | 50862 |
rs184188498 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512099 | CTGAGTTAGGATAGG[A/G]AAAACAAATTCCTTA | 50862 |
rs184201442 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10532988 | GTCCAATCCTTAGCA[G/T]AGGGCCTTGCACATA | 50862 |
rs184507036 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10524359 | GGCAGAGCTTGCAGT[C/G]AGCCGAGATCGCGCC | 50862 |
rs184656785 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10528133 | TTAAATATTATTTAA[A/G]GATAATCATAGCAGA | 50862 |
rs184708595 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10528772 | TGTTCACTTAATATA[C/T]ACTGAGTTCCTACTA | 50862 |
rs184730714 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | RNF141 | GRCh38.p7 | 11:10517882 | TTGATATACAAATAT[C/G]TATTGTATTTCCATA | 50862 |
rs184970122 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10525694 | TCAGTATTAACAATT[A/C]TTTCACTTTAATTTC | 50862 |
rs185362601 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | RNF141 | GRCh38.p7 | 11:10516577 | ATTCCAGAGGTCTAC[A/G]GAAGTGTCCCCGCCA | 50862 |
rs185484762 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10538856 | TACTATTTGATTTTA[A/C]CAAGATACTCCCCCC | 50862 |
rs185523994 | snp | A/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514641 | GTTGCTGTTACCTTT[A/T]GCAAAGAATTCAAGA | 50862 |
rs185560889 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10535017 | GTACCCCCAAAATAT[A/G]TATCTAATTATCAAG | 50862 |
rs185630785 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512774 | TTAAAAAATTTTTTT[A/T]AAAAAAACGACTCCC | 50862 |
rs185710697 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10530551 | ACCGAGTTATTAAAA[C/T]GTATATGCATTATAT | 50862 |
rs185738028 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10529072 | AGAAACTACTGGCTG[A/C]TTATCCAAATACCAT | 50862 |
rs185799465 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10526730 | GAGGTTGCAGTGAGC[A/C]GAGATGGCGCCACTG | 50862 |
rs185800465 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10527868 | GCGTAGATGGTGAGA[C/G]CTAGCCAGATTCTGA | 50862 |
rs186371493 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10526081 | CATAATGAAATGACC[A/G]AGGCCAGTAAGGTGA | 50862 |
rs186488322 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520792 | TTAGGATGGCTACGA[C/T]GTCCACAGGCAATAG | 50862 |
rs186499095 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542397 | ACACTGGAAAAGGAA[A/G]AAGCTTAAAAATGAA | 50862 |
rs186544087 | snp | C/G | 0.00953873 | 0.0683987 | intron-variant | RNF141 | GRCh38.p7 | 11:10521828 | CTGGCATGATACTTG[C/G]GTATGGAAAACTGAG | 50862 |
rs186576077 | snp | A/G | 1.65048e-05 | 0.00287265 | missense | RNF141 | GRCh38.p7 | 11:10519104 | CCCGCCCATCCATAC[A/G]GATACAACACTCCTC | 50862 |
rs186612660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515752 | CATGACTTTCAACAA[C/T]ATATCTACCTGTTGC | 50862 |
rs186628646 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10537462 | TGAACTTTTGAAATA[C/T]ATAGTCTCAATATTT | 50862 |
rs186699462 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527105 | CACACTGTAACTATT[C/G]TCATCATAGGATTCC | 50862 |
rs186774127 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541647 | CTAGCCGAGTTGTTA[A/C]GCATAAGAGAATGTA | 50862 |
rs187124026 | snp | A/G | 0.00478085 | 0.0486577 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511778 | ATATATTAGATATAA[A/G]GAAATCGAGTCCAAT | 50862 |
rs187138594 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532191 | ATGGTAAATGTCATT[C/G]ATTACTGCTCATAAG | 50862 |
rs187150467 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10536689 | GTCTGGTAACAAACT[C/T]CTGGGCTCAAGCAAT | 50862 |
rs187311313 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538771 | CAGAAGTTAAAAATA[C/T]GTATGAAAGAAAATG | 50862 |
rs187370695 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514854 | GTGCCACAACCCTAC[A/G]TTCTTCCCCCATGAC | 50862 |
rs187392765 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533267 | ATTCAGGAACAAAGA[A/G]CCCTATATATTTTCA | 50862 |
rs187423531 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512246 | TGTACATTTCATCCA[C/T]TAAACAAATTTACAA | 50862 |
rs187487365 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10527937 | AGGTGTGAGAGACAA[A/G]GAAAAGCCAAGAATG | 50862 |
rs187723260 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | RNF141 | GRCh38.p7 | 11:10527344 | ACGCTGAGGGGTTAC[A/G]GGGAAGGCCTTACAG | 50862 |
rs187857245 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10523434 | CATATGGGGTTGTGA[G/T]AATTTAATGAGTTTA | 50862 |
rs188044509 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539828 | AAGCATATTAGACTT[C/G]TAAGAATTCTCTCTG | 50862 |
rs188120679 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516228 | CAAAACATCACAATT[G/T]AAAAATAGTCAACTT | 50862 |
rs188196837 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10534327 | GAGTAGACCTACATG[A/T]GTCTAAGGTAGAATT | 50862 |
rs188199671 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10522353 | AAAGAATGGGAGATA[A/C]AGAAATAGCCAGTGG | 50862 |
rs188205028 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513904 | TGGTCTCAAACTCCT[A/G]ACCTCAAATGATCCA | 50862 |
rs188396303 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10539016 | TAACACAGTCATTTT[G/T]TGCAAGATAAAAATA | 50862 |
rs188807933 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528180 | AAAAGACTTAATGTA[A/C]ATACAGAGGGTTAAA | 50862 |
rs189026291 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516703 | GCTCACTGGGCCTGG[A/G]ATACTGCCTGTTTCA | 50862 |
rs189075974 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | RNF141 | GRCh38.p7 | 11:10528800 | CTATGTGTAAAGCAC[C/T]GTATTACAGCCTGTA | 50862 |
rs189096865 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | RNF141 | GRCh38.p7 | 11:10529214 | TATTCCCTCTGTCAG[C/T]GTAGGTGTATGAAGG | 50862 |
rs189167758 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | RNF141 | GRCh38.p7 | 11:10531158 | AAGGCAGGCAGATCA[C/T]GAGGTCAGGAGTTCG | 50862 |
rs189491054 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10524895 | AACCTAAATACCTAT[C/T]ATAAGGAAGGTGTTA | 50862 |
rs189644816 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10526451 | TTTATTAATTGCTTA[C/T]TATTTGAAAAGGCAG | 50862 |
rs189749570 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542913 | ATCAACCCAGGTGCT[C/T]ATCAATAGTGGATTG | 50862 |
rs189774798 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10518557 | TGTATATATGCCAAA[A/T]CATATTAAACTGTAC | 50862 |
rs189788599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521446 | TCTTCATCAGACATG[C/T]ATTACTTTTGTAATA | 50862 |
rs189854253 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | RNF141 | GRCh38.p7 | 11:10526041 | GAGATTGCTTTCACA[A/G]GCTTTGGGGAGCCAT | 50862 |
rs189899995 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10537997 | CTTTTAACTCAAAAT[A/G]ATCCTTATGCCAAAG | 50862 |
rs189935918 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10516002 | CCAGAGACATATTAT[A/G]CAGAGAAAAATGTTT | 50862 |
rs190004325 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540122 | GACTAATTTAGGATC[A/G]TCGGCCGGTGGCAGC | 50862 |
rs190251268 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10519581 | TTATACAAACCTAGA[C/T]GGTTTAGCCTACTAC | 50862 |
rs190298219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10530227 | AATTACTAAAAAACA[A/G]AAAAACTCTTTCAAT | 50862 |
rs190401549 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10527150 | ATTGAGTACCATTAT[A/G]TGGATGTTATTGGTA | 50862 |
rs190506337 | snp | C/T | 0.00676609 | 0.0577691 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512881 | ATCACATTTATAGTA[C/T]ATAAAGTTTATATAA | 50862 |
rs190564092 | snp | C/T | 0.00105633 | 0.0229576 | intron-variant | RNF141 | GRCh38.p7 | 11:10530631 | AGAGGTAGAAGTCTC[C/T]ATCAGTCTCACCTTG | 50862 |
rs190716269 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10531408 | AGCTAGTGTCATTTA[C/T]CAAAATTTTTTGACT | 50862 |
rs190807752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10533703 | CCCCTTTAGTGCTTT[C/T]AAACAAGAGTCTATT | 50862 |
rs190938615 | snp | G/T | 0.000798403 | 0.0199641 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511335 | CGCATACGAGGGATC[G/T]AGGTTGCATGCACCT | 50862 |
rs191051894 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526777 | ACAGAGCAAGACTAC[A/G]TCTCAAAAAAAAAAA | 50862 |
rs191262021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10523923 | AAAGACAAGCCTAAA[C/T]ACTGCCTACCATGTT | 50862 |
rs191354239 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521904 | GTCAAAATATTAAGT[C/T]TGAACGTGTCCTGAC | 50862 |
rs191393401 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539909 | ACCAAGAAGGATCAG[A/G]CTACACACATCGAAT | 50862 |
rs191493370 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10535550 | TCCAAGAAGAAACAA[C/T]TAAAGATCTTAGCTT | 50862 |
rs191619299 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532566 | TACAGCTTTTTGTTT[C/T]ATATTGTTTTGTTTT | 50862 |
rs191643044 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511954 | GCGAAAGATTATTTA[C/T]TGCACAATTTATCAG | 50862 |
rs191766011 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514743 | TTTAGTACCACAAAT[A/G]GAAGACATGGGAAGT | 50862 |
rs192094302 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10515270 | TTATATATTCCTCCA[A/G]AGATAGACTAAGCTG | 50862 |
rs192114893 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10528752 | TTATTTCAACAGATT[C/T]TTTTTGTTCACTTAA | 50862 |
rs192146645 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523192 | GCAGCATTGGCCCCA[C/G]CTGGGAGCTTGACAG | 50862 |
rs192332760 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10527449 | TGAGACAACAGGAAA[C/T]ACAAAGGCTGTTTAA | 50862 |
rs192346500 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516857 | CAAAAGCAAGATCCA[A/G]AAGAATCAAACTGTT | 50862 |
rs192494708 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10536891 | CCATTATGCTTTGCA[A/G]TGGTTAGGCCACACT | 50862 |
rs192535512 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10525512 | TACATAAGAAAGCAA[A/G]AGTCTGAATAAATGA | 50862 |
rs192759164 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528031 | AGCCACCTTAGTACC[C/T]AGTTTTTAATTAATC | 50862 |
rs192890022 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538832 | TGCTTATGTAAACTG[A/G]GAAACATTTACTATT | 50862 |
rs192936200 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512517 | TGGGGGATAAAATCA[A/T]TGGCTATCCCTGGAA | 50862 |
rs193068526 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | RNF141 | GRCh38.p7 | 11:10516427 | CCTCGAGAGTTTCTA[A/G]CCCCTGATCAAGAAG | 50862 |
rs193173472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10533526 | TCTAGCAAAATGATG[A/G]CACAGTAAAAAAAAG | 50862 |
rs193214998 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539272 | CCTAAAAATTTAAAC[A/C]ATAATTCATTCATAA | 50862 |
rs199565052 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523746 | GAAGACTGTAACAAG[A/G]AAAAAACAATACTTT | 50862 |
rs199623600 | snp | C/T | 0.000155423 | 0.00881404 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514884 | CCAAATATTTGAGCC[C/T]ACAATAGCAACAGAA | 50862 |
rs199626076 | in-del | -/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10535355 | AAAGGACAATTGTAA[-/T]TTAAAAAAAAAACAA | 50862 |
rs199653302 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523752 | TGTAACAAGAAAAAA[A/C]CAATACTTTCTTTTC | 50862 |
rs199671583 | snp | A/C | 0.000115421 | 0.00759587 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10515042 | CTGTAGGCGACAAAT[A/C]GGGCAATTCCTGTGT | 50862 |
rs199746434 | in-del | -/T | 0.125182 | 0.216612 | intron-variant | RNF141 | GRCh38.p7 | 11:10519665 | TAGCATGTTACTGTA[-/T]GGAACACTGTAGGCT | 50862 |
rs199756415 | in-del | -/A | 0.238749 | 0.249747 | intron-variant | RNF141 | GRCh38.p7 | 11:10535356 | AGGACAATTGTAATT[-/A]TAAAAAAAAAACAAA | 50862 |
rs199759836 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10538374 | TAACATCTATCACTA[G/T]ATGGGTGTGAAAATA | 50862 |
rs199911406 | snp | A/G | 0.000165505 | 0.00909534 | utr-variant-5-prime | RNF141 | GRCh38.p7 | 11:10534168 | TCCCATGATGAAAAG[A/G]TGTCTTTCAAAATCC | 50862 |
rs199927970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10530604 | TTCTAGCCACCAAAA[C/T]AGCTTAAGCTCAGAG | 50862 |
rs199980482 | in-del | -/AC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518869 | ATGTTAGGTGTAAAA[-/AC]AAAAATAGTTTTAAC | 50862 |
rs200014417 | in-del | -/TG | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520262 | CTTTTTGACTCTTTT[-/TG]TAACAACACTTACCT | 50862 |
rs200084290 | snp | A/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10534237 | AAAGTTACTTTTACA[A/T]ATTATACAAAAACGG | 50862 |
rs200210877 | in-del | -/ATG | 0.0154538 | 0.0865337 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541712 | TGATAAATGATAGAT[-/ATG]ATGATGATGAGCACA | 50862 |
rs200243664 | in-del | -/TCCCTGAAGTC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10535481 | AAAAAAAAAAAAAAA[-/TCCCTGAAGTC]AAATTATATGTAAAT | 50862 |
rs200292658 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540623 | CTAAGTAGATCGACG[A/T]GGCTATTTCTGAGCT | 50862 |
rs200322677 | in-del | -/GCGCACAATAT | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511838 | CATCACAAGCCCCCA[-/GCGCACAATAT]AAAATAGTTCTCTAA | 50862 |
rs200448268 | snp | C/G | 3.29723e-05 | 0.00406018 | missense | RNF141 | GRCh38.p7 | 11:10525236 | TGTTACAGAGGATGA[C/G]TTTTCATCAGGTTCT | 50862 |
rs200616934 | in-del | -/AAAG | 0.0256215 | 0.110247 | intron-variant | RNF141 | GRCh38.p7 | 11:10519384 | GATACATTTTGTGAT[-/AAAG]AAAACATAGGCAAAA | 50862 |
rs200706073 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10524417 | TTAAAAAAAAAAAAA[-/A]TCACTGTTAAGTACA | 50862 |
rs200732979 | in-del | -/AACT | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10517071 | ATCATAACCACCCAG[-/AACT]AACACAGATATTAGA | 50862 |
rs200756768 | in-del | -/AA | 0.125874 | 0.217008 | intron-variant | RNF141 | GRCh38.p7 | 11:10519668 | CATGTTACTGTATGG[-/AA]CACTGTAGGCTACTG | 50862 |
rs200764136 | in-del | -/AAC | 0.0298908 | 0.118541 | intron-variant | RNF141 | GRCh38.p7 | 11:10535373 | AAAAAAAAAACAAAA[-/AAC]AACAGTTTTGAATCT | 50862 |
rs200883825 | snp | A/G | 3.30022e-05 | 0.00406202 | missense | RNF141 | GRCh38.p7 | 11:10519092 | GGATGAGGTCAGCCC[A/G]CCCATCCATACAGAT | 50862 |
rs200956762 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10525081 | TACAATACCAACTGA[A/G]AAAAAAAAAAGATTT | 50862 |
rs200958771 | snp | C/G | 0.000399281 | 0.0141238 | missense | RNF141 | GRCh38.p7 | 11:10534072 | AGTTAAGGAGCCACT[C/G]TCTCGAACCAACGTA | 50862 |
rs200993727 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523753 | GTAACAAGAAAAAAA[A/C]AATACTTTCTTTTCA | 50862 |
rs201066765 | in-del | -/A | 0.030278 | 0.119257 | intron-variant | RNF141 | GRCh38.p7 | 11:10533532 | AAATGATGACACAGT[-/A]AAAAAAAAGTATATA | 50862 |
rs201354434 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10534478 | CACATGTGCATGTGT[A/G]CACACACACACACAC | 50862 |
rs201477257 | in-del | -/AAA | | | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542788 | ATATCTCTTATCAGC[-/AAA]AAAAAAAAAAAAAAA | 50862 |
rs201480043 | in-del | -/GT | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513231 | TCTTCAGTATTTTTG[-/GT]GGGGCGAAATCAAGC | 50862 |
rs201490349 | in-del | -/T | 0.125874 | 0.217008 | intron-variant | RNF141 | GRCh38.p7 | 11:10519670 | GTTACTGTATGGAAC[-/T]ACTGTAGGCTACTGT | 50862 |
rs201491735 | in-del | -/ATGG | | | intron-variant | RNF141 | GRCh38.p7 | 11:10519664 | ATAGCATGTTACTGT[-/ATGG]AACACTGTAGGCTAC | 50862 |
rs201522796 | snp | A/G | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513811 | CCTCCCGAGTAGCTG[A/G]GATTACAGGCACCTG | 50862 |
rs201572891 | snp | C/T | 3.82336e-05 | 0.00437211 | intron-variant | RNF141 | GRCh38.p7 | 11:10530794 | TTATGAAAAATCATA[C/T]ATTAATAAAATAATA | 50862 |
rs201745825 | snp | A/G | 0.000661726 | 0.0181776 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10519039 | GGTAACTTACCATTT[A/G]TCAATACACTTCTGA | 50862 |
rs201813387 | in-del | -/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10527655 | AGTCACGGGGGGGGG[-/T]TTTGAGCCAAGGAGT | 50862 |
rs201847988 | in-del | -/CACCAC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520426 | AAACAGCGTCAGGAT[-/CACCAC]CATCACTGTCTTCCG | 50862 |
rs201969020 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10534479 | ACATGTGCATGTGTA[C/T]ACACACACACACACA | 50862 |
rs202011391 | in-del | -/T | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539699 | ATACATACATATATA[-/T]TAGAGAGAGAAGGAG | 50862 |
rs202027110 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10524999 | TTAAAGTGGCCCTGC[G/T]AAGCCACTTTAATTT | 50862 |
rs202148064 | in-del | -/ACAC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10534478 | CACATGTGCATGTGT[-/ACAC]ACACACACACACACA | 50862 |
rs202174143 | in-del | -/CC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532541 | ACACACACACACCCC[-/CC]ACAACTATATACAGC | 50862 |
rs202208761 | in-del | -/AGC | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511818 | TTTTAAAACAGCACA[-/AGC]CAAACATCACAAGCC | 50862 |
rs202213243 | snp | C/T | | | utr-variant-5-prime | RNF141 | GRCh38.p7 | 11:10534173 | TGATGAAAAGATGTC[C/T]TTCAAAATCCAGAGT | 50862 |
rs367611654 | snp | C/T | | | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541283 | GGCGCCCAACCTTCC[C/T]CTGCAGCGCCCCTAC | 50862 |
rs367617165 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10537893 | CTGGCATAGAGAGGA[C/T]ATCTTTCACATGGCT | 50862 |
rs367678075 | in-del | GG/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10527651 | GAGAAGTCACGGGGG[GG/T]GGTTTTGAGCCAAGG | 50862 |
rs367876522 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523758 | AAGAAAAAAACAATA[C/T]TTTCTTTTCATGTGC | 50862 |
rs367997885 | snp | C/G | 0.000132558 | 0.00814011 | intron-variant | RNF141 | GRCh38.p7 | 11:10530599 | TATAGTTCTAGCCAC[C/G]AAAATAGCTTAAGCT | 50862 |
rs368165664 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10536438 | TGCCTGCCCAATCTG[C/T]GGATGACCAAAACTG | 50862 |
rs368323419 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10515608 | AGATTTGGTCAAAGT[G/T]TCAAGTATAAATGCT | 50862 |
rs368380848 | snp | A/C | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512304 | CTGACCTAACATTCA[A/C]ATCTAAATAATTATC | 50862 |
rs368466513 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10521232 | GGTAACTCAGCTCAA[A/G]ACATCATCATCTCTC | 50862 |
rs368635809 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539741 | AAAAGGATAGAGTGC[C/T]GTACTAGGAGATTAA | 50862 |
rs368653526 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520774 | ATGCATTGCATCACA[A/G]TATTAGGATGGCTAC | 50862 |
rs368701893 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541008 | GGGCTAGGCCTGTCT[A/C]CCCGCGGAAGCCTGG | 50862 |
rs368709500 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10521932 | GACAAGCAAACTACA[A/G]TCAGTGTATAATCAA | 50862 |
rs368797758 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10536989 | GGCATAGAAAAAAAA[-/A]GAGGTTTATTCTAGA | 50862 |
rs368916662 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10524948 | GCATGCATATAGAGC[A/G]GATTCCTGGAGACCA | 50862 |
rs369036739 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10516300 | AAATTACTAAAACAA[C/T]GGTTTCATACAATCT | 50862 |
rs369199259 | in-del | -/CTGGCT | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540723 | GCGCTCGCTCTGGCT[-/CTGGCT]ACGCCGCCTCAGCCC | 50862 |
rs369437130 | snp | A/G | 1.656e-05 | 0.00287745 | intron-variant | RNF141 | GRCh38.p7 | 11:10515069 | GTGTCGATCACTCCT[A/G]TTAGAGAAGTCAAAA | 50862 |
rs369683849 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531625 | ATTTAGAGAGCTAAA[G/T]GATTTAAACATAAAA | 50862 |
rs369849977 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518299 | ACTTGTCCATGAATG[C/T]ATCTAGTACCTTTAT | 50862 |
rs370073182 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | RNF141 | GRCh38.p7 | 11:10533722 | CAAGAGTCTATTGGT[A/G]TAAAATTGAGATGCT | 50862 |
rs370299041 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10526063 | GGGAGCCATGGAGTG[A/C]GGCATAATGAAATGA | 50862 |
rs370469610 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541972 | TTGTACACCCCTCCT[C/T]CACCAGTCACTTGTA | 50862 |
rs370640929 | snp | A/C | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514644 | GCTGTTACCTTTAGC[A/C]AAGAATTCAAGAGCT | 50862 |
rs370652100 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518638 | TCAAGTCTTATTTTG[C/T]AAAATAATGAACTTG | 50862 |
rs370677154 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518878 | GTAAAAACAAAAATA[C/G]TTTTAACCAGTAGAA | 50862 |
rs370994212 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10533221 | TAAATAGCAAAAAAG[C/T]CATATTTTAAAAGCA | 50862 |
rs371034970 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516876 | AATCAAACTGTTTCC[A/G]AGTCACTTAACTATA | 50862 |
rs371061738 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10525650 | TGGGTAAGGTGACTT[C/T]CTCAGAGTTAAGAAA | 50862 |
rs371158563 | snp | A/C/G/T | 0.000132276 | 0.00813154 | missense, synonymous-codon | RNF141 | GRCh38.p7 | 11:10519123 | ACAACACTCCTCCTC[A/C/G/T]TCGGTCAGCTGCTTC | 50862 |
rs371233657 | snp | A/C | 3.31422e-05 | 0.00407063 | utr-variant-5-prime | RNF141 | GRCh38.p7 | 11:10534176 | TGAAAAGATGTCTTT[A/C]AAAATCCAGAGTGTT | 50862 |
rs371666288 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10530588 | ACAGTATTAAATATA[C/G]TTCTAGCCACCAAAA | 50862 |
rs371671959 | in-del | -/TTTT | 0.00716266 | 0.059414 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539574 | TAAACAGATATCAAC[-/TTTT]TTTTTTCAAGACAAG | 50862 |
rs371755529 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10517745 | ACTCTCAAGTCTAGA[-/A]TTCTGAATCAGAAAA | 50862 |
rs371796921 | snp | C/T | 0.000153988 | 0.00877328 | missense | RNF141 | GRCh38.p7 | 11:10534076 | AAGGAGCCACTCTCT[C/T]GAACCAACGTAACAT | 50862 |
rs372137795 | snp | A/C | 1.67984e-05 | 0.00289809 | intron-variant | RNF141 | GRCh38.p7 | 11:10533980 | GGCATACATACAACA[A/C]GGGGAAAAACGAAAA | 50862 |
rs372272833 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533576 | GTGTGTCTATATACA[A/C]ACACACATGAATGAA | 50862 |
rs372689336 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10537748 | AACATGACAAGACAC[A/G]AGGGTTTGGGCTGGG | 50862 |
rs372692868 | snp | A/C | 0.000153988 | 0.00877328 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514893 | TGAGCCCACAATAGC[A/C]ACAGAAGACTTTCAC | 50862 |
rs372735771 | snp | A/C | 0.0295035 | 0.117819 | intron-variant | RNF141 | GRCh38.p7 | 11:10523831 | TTTAAAACAATTAAA[A/C]AAAACAACAACCACT | 50862 |
rs372755617 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531436 | ACTGTTGCCTCAGAC[A/G]TATATAAAGCATGAA | 50862 |
rs372794064 | in-del | -/ATTTTT | 0.00636936 | 0.0560724 | intron-variant | RNF141 | GRCh38.p7 | 11:10524806 | ATGCTTCAATTAGAC[-/ATTTTT]ATTTTTTAAAAAAAG | 50862 |
rs372833006 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10536840 | AATCCTAAACTCTTG[A/C]TAGAAGCAGGTATCT | 50862 |
rs372864425 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10527073 | TATAAGGTCAGTACA[A/G]AAATAGCAAAGTGTA | 50862 |
rs372912699 | snp | C/G | 1.64836e-05 | 0.0028708 | missense | RNF141 | GRCh38.p7 | 11:10534133 | TTAATAACCAACTGT[C/G]TCTGATCCGAAATTT | 50862 |
rs372917792 | snp | A/G | | | missense | RNF141 | GRCh38.p7 | 11:10534082 | CCACTCTCTCGAACC[A/G]ACGTAACATGTTTTG | 50862 |
rs373485913 | in-del | -/GG | | | intron-variant | RNF141 | GRCh38.p7 | 11:10527654 | AGTCACGGGGGGGGG[-/GG]TTTTGAGCCAAGGAG | 50862 |
rs373497933 | snp | C/T | 6.9365e-05 | 0.00588877 | intron-variant | RNF141 | GRCh38.p7 | 11:10518984 | AAGTTTATTCATGTA[C/T]ACTATCCCACTGACC | 50862 |
rs373725895 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532539 | CACACACACACACAC[A/C]CCACAACTATATACA | 50862 |
rs373803578 | snp | C/T | 4.94507e-05 | 0.00497221 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10525311 | GATATCTTTATAAAG[C/T]TGAATAAACTGGTAT | 50862 |
rs373805913 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514849 | TGCCAGTGCCACAAC[C/T]CTACATTCTTCCCCC | 50862 |
rs374092314 | in-del | -/TCGGCCTCCCAGGCC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10536714 | AGCAATCCTCCCGCC[-/TCGGCCTCCCAGGCC]GAGGATTACAGGCAT | 50862 |
rs374192002 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10530224 | AAAATTACTAAAAAA[-/A]CAAAAAAACTCTTTC | 50862 |
rs374260657 | snp | A/C | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540292 | TATATGCCAGAGGCA[A/C]GAACTGAATTAGCTG | 50862 |
rs374286180 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520418 | CTAGGCCTAAACAGC[A/G]TCAGGATCACCACCA | 50862 |
rs374460916 | snp | C/G | | | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542413 | AAGCTTAAAAATGAA[C/G]TATAAATAATGATTT | 50862 |
rs374476002 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513154 | TCTGCTTGCATAAAC[C/T]TCCATAGGGAGTAGT | 50862 |
rs374591437 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533251 | ACAGTGGTCTGGGGG[C/T]ATTCAGGAACAAAGA | 50862 |
rs374751303 | in-del | -/A | 0.0107246 | 0.0724382 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514696 | TTTGAACAGATAAAT[-/A]ATAGGAAAATATGGT | 50862 |
rs374806365 | in-del | -/ACTGTATGGAAC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10519659 | CATATATAGCATGTT[-/ACTGTATGGAAC]ACTGTAGGCTACTGT | 50862 |
rs374902877 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10537116 | TGGCCACTAAGTATA[A/G]TAAGTATAAATTAGA | 50862 |
rs375021107 | snp | A/C | 1.65086e-05 | 0.00287298 | intron-variant | RNF141 | GRCh38.p7 | 11:10530634 | GGTAGAAGTCTCCAT[A/C]AGTCTCACCTTGGTA | 50862 |
rs375141342 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531235 | CAAAAATTAGCCGGG[C/T]GTGGTGGCGTACACC | 50862 |
rs375145195 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514076 | ATATTAAATGACCTA[C/T]AGTAATTTAGAAATA | 50862 |
rs375147136 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10538988 | AGCAGCTCTCATATT[A/G]TTGTGCCACCTATAA | 50862 |
rs375178728 | in-del | -/AA/AAA/AAAA | 0.0752113 | 0.178743 | intron-variant | RNF141 | GRCh38.p7 | 11:10531374 | GTGAGACTCAGTCTC[-/AA/AAA/AAAA]AAAAAAAAAAAAAAG | 50862 |
rs375208237 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10537793 | AAAAGTGACTAGGAA[C/G]ATAAGGGTTACTTTA | 50862 |
rs375253298 | in-del | -/GAAA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10519387 | ACATTTTGTGATAAA[-/GAAA]ACATAGGCAAAAGTG | 50862 |
rs375380846 | snp | A/C/G/T | 0.000149069 | 0.00863223 | intron-variant | RNF141 | GRCh38.p7 | 11:10534010 | AACAAAAAGAGCAAG[A/C/G/T]CTTACACATCATTAA | 50862 |
rs375542152 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520364 | TTTTTACTTTCTAAA[C/G]TTTTTTCTTAAAAAC | 50862 |
rs375650940 | snp | C/G | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511812 | AAATGAATTTTAAAA[C/G]AGCACACAAACATCA | 50862 |
rs375712983 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539687 | GATCAGAAAAAGATA[C/T]ATACATATATATTAG | 50862 |
rs375787316 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513264 | CCCCTGGCCAGATGT[C/T]TTTCCTTGAAATTGA | 50862 |
rs375915889 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526004 | TACAATCTAATGTAG[A/C]AGATACTTGGGGCAA | 50862 |
rs376221034 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10535863 | TCTTGATCGAATCCA[A/G]ACTTATGAAAACATC | 50862 |
rs376226428 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10519135 | CTCATCGGTCAGCTG[C/T]TTCACCCTGCAATGT | 50862 |
rs376476071 | snp | C/T | | | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511586 | CATGAATGTGAGTGA[C/T]CTGTTAACTTCCCTC | 50862 |
rs376501592 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10523931 | GCCTAAACACTGCCT[A/G]CCATGTTCTAAAAGT | 50862 |
rs376599478 | snp | C/G | 1.64803e-05 | 0.00287052 | missense | RNF141 | GRCh38.p7 | 11:10525247 | ATGAGTTTTCATCAG[C/G]TTCTTCAGAGGTGGA | 50862 |
rs376839601 | snp | C/T | | | synonymous-codon | RNF141 | GRCh38.p7 | 11:10519090 | CAGGATGAGGTCAGC[C/T]CGCCCATCCATACAG | 50862 |
rs377017497 | snp | C/T | 9.89381e-05 | 0.00703273 | synonymous-codon | RNF141 | GRCh38.p7 | 11:10534141 | CAACTGTGTCTGATC[C/T]GAAATTTGCTGTCCC | 50862 |
rs377165542 | snp | C/T | 0.00059455 | 0.0172314 | missense | RNF141 | GRCh38.p7 | 11:10515058 | GGGCAATTCCTGTGT[C/T]GATCACTCCTATTAG | 50862 |
rs377189375 | snp | A/G | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514112 | TTTAGTATTTGTGAT[A/G]CAGAATAATTTCCTT | 50862 |
rs377217140 | in-del | -/GAGA | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539716 | AGAGAGAGAAGGAGA[-/GAGA]AACTACAAAAGGATA | 50862 |
rs377333979 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10528754 | ATTTCAACAGATTTT[C/T]TTTGTTCACTTAATA | 50862 |
rs377556966 | snp | A/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518441 | GATACATGCTACAAC[A/T]TGAATAAATACCAAG | 50862 |
rs377654959 | snp | A/C/T | 1.6519e-05 | 0.00287388 | missense, stop-gained | RNF141 | GRCh38.p7 | 11:10519116 | TACAGATACAACACT[A/C/T]CTCCTCATCGGTCAG | 50862 |
rs377718978 | snp | A/G | 0.000153988 | 0.00877328 | missense | RNF141 | GRCh38.p7 | 11:10534142 | AACTGTGTCTGATCC[A/G]AAATTTGCTGTCCCA | 50862 |
rs377731136 | in-del | -/AG | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10529739 | ATAATCTGGATCAGA[-/AG]AGAGAGATCAGTCTG | 50862 |
rs377748773 | snp | A/C | 3.34152e-05 | 0.00408736 | intron-variant | RNF141 | GRCh38.p7 | 11:10519145 | AGCTGCTTCACCCTG[A/C]AATGTGAAAACTGAG | 50862 |
rs386373086 | in-del | -/AAA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531375 | TGAGACTCAGTCTCA[-/AAA]AAAAAAAAAAAAAGG | 50862 |
rs386373087 | in-del | -/AAA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531386 | CTCAAAAAAAAAAAA[-/AAA]AAGGTTAGCTAGTGT | 50862 |
rs386373088 | in-del | -/AA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531387 | TCAAAAAAAAAAAAA[-/AA]AGGTTAGCTAGTGTC | 50862 |
rs386373089 | in-del | -/AT | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533553 | AAGTATATATATATA[-/AT]TGCATGTGTGTGTCT | 50862 |
rs386750615 | multinucleotide-polymorphism | CTTC/TTTT | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532125 | TGCTAAAGGGCAAAA[CTTC/TTTT]ATACAATAGACAGGG | 50862 |
rs386750616 | multinucleotide-polymorphism | AATAC/GACTG | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539497 | ATACCAAGTACTACT[AATAC/GACTG]GGTCCCTAAGGATAT | 50862 |
rs397700301 | in-del | -/AT | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10533554 | AGTATATATATATAT[-/AT]GCATGTGTGTGTCTA | 50862 |
rs397726595 | in-del | -/A | 0 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10525091 | CTGAGAAAAAAAAAA[-/A]GATTTAAGATGCTAC | 50862 |
rs397755075 | in-del | -/C | 0.375 | 0.216506 | intron-variant | RNF141 | GRCh38.p7 | 11:10527654 | CTCCTTGGCTCAAAA[-/C]CCCCCCCCGTGACTT | 50862 |
rs397814351 | in-del | -/A | 0.5 | 0 | intron-variant | RNF141 | GRCh38.p7 | 11:10535367 | AATTTAAAAAAAAAA[-/A]CAAAAAACAACAGTT | 50862 |
rs397848273 | in-del | -/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513697 | CTTGTGTTTTTTTTT[-/T]GATTAGGAGTCTCGT | 50862 |
rs397848369 | in-del | -/AC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10534502 | CACACACACACACAC[-/AC]GCATTCAAGTAATTG | 50862 |
rs397849506 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523752 | TGTAACAAGAAAAAA[-/A]CAATACTTTCTTTTC | 50862 |
rs398054991 | in-del | -/AA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518868 | AATGTTAGGTGTAAA[-/AA]CAAAAATAGTTTTAA | 50862 |
rs527243797 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542037 | ATAATAATACTCTTT[A/G]ACCATTTACTATATG | 50862 |
rs527244340 | snp | A/G | 8.36197e-05 | 0.00646551 | intron-variant | RNF141 | GRCh38.p7 | 11:10533991 | AACAAGGGGAAAAAC[A/G]AAAAACAAAAAGAGC | 50862 |
rs527473519 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513347 | ATCAATAAGTGGCAA[C/T]TTAAATTGTGTACCC | 50862 |
rs527568620 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532459 | CCACCATCTCCCAAC[C/T]GAGAGACAAGCACTG | 50862 |
rs527714189 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10515820 | GCAACAGGAAGACTT[-/A]TATAAAAATGGAGCA | 50862 |
rs527762932 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542972 | ATGGAATACTATACA[A/G]CCACAAAAAGGACTA | 50862 |
rs527850342 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10522014 | GCAGTATGAGGGACA[C/G]TCTAGAAAGAGGAAA | 50862 |
rs527915223 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10527716 | ATGTGGAATAGGCTG[C/G]TTGTTGTGCTTGGAA | 50862 |
rs528124326 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522777 | ATAGACAAATTATTA[C/T]GTGTCAAGCACTGTT | 50862 |
rs528165296 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517438 | AGAGGGGAGAGAAGA[C/T]AGAAAAAAATCTGAA | 50862 |
rs528840126 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512757 | ATTTGACTTGAATTT[A/C]ATTAAAAAATTTTTT | 50862 |
rs529005875 | in-del | -/GCCGAGATC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10524361 | CAGAGCTTGCAGTGA[-/GCCGAGATC]GCGCCTGGGCGACAG | 50862 |
rs529052769 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10518407 | GACATTACTCAGCAA[C/T]AAAAAGGCATGAACT | 50862 |
rs529112949 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531902 | CTAGCTGCCAAGCTT[C/T]GTCCTGTATAGGTTT | 50862 |
rs529194475 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10517231 | AAATTATCTGAGGTT[-/A]AAAAAAATACACTGG | 50862 |
rs529254399 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10515927 | TAAGATTATGTTTTC[A/G]AAAAGGATTTTTTTC | 50862 |
rs529305714 | snp | A/C | | | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541965 | TTCTTGTTTGTACAC[A/C]CCTCCTTCACCAGTC | 50862 |
rs529406436 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541487 | AAAGTGGAGCGCCCC[G/T]CTGGCGACCAAGGCC | 50862 |
rs529489425 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540837 | TTTTGGGATAGAGAA[A/G]GAAAAACTCTCTCCG | 50862 |
rs529490515 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542090 | TAAAGGTATTAATTC[A/G]TTTAATCTTCACAGC | 50862 |
rs529578086 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10533810 | CCATTTTAAGTTCTT[C/T]CCATATCTTCTGTCC | 50862 |
rs529639385 | in-del | -/A | 0.00438332 | 0.0466095 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542512 | GAAATATTACTCTGT[-/A]AAAATTGCCTTCAAT | 50862 |
rs529672381 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10535599 | AGTCAACAACAGTGA[C/T]TGCTGAATTTCAAAG | 50862 |
rs529741139 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514542 | CAACTTTTTAATATT[C/T]GAGGTTTATTTTATA | 50862 |
rs529745266 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10534705 | ACTGAGCTAGGTGAT[C/T]TATCTAAAGTTACAC | 50862 |
rs529898397 | snp | A/G/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10527564 | GAGTGGTAGATAGAC[A/G/T]GTGAGGTGGGAATAG | 50862 |
rs529918602 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10524362 | AGAGCTTGCAGTGAG[C/G]CGAGATCGCGCCTGG | 50862 |
rs530229606 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515421 | ACACTGTATCGCTAT[A/G]CCATAATTTGTTTAA | 50862 |
rs530313388 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522555 | GGAAAGCCTCCAGTA[G/T]GTAGACGAGACCCAC | 50862 |
rs530504240 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517530 | TCAATAAACCCCAAG[C/T]ACAAGAAACATGAAA | 50862 |
rs530529537 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10518197 | TGGCAGCTTTTTAAA[A/G]AGTTAAACACACACA | 50862 |
rs530593395 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511228 | GCAGGAGTTGAGCCG[C/T]GGGCGAGTGAGTATT | 50862 |
rs530610917 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10529578 | AGGAGTTGGGACTAT[G/T]TGGTAGGCAAGAAGG | 50862 |
rs530612437 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538101 | GTTATTAATAGAAAA[C/T]GATCCCCTTTGTTTC | 50862 |
rs530648475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10537092 | AAGATTCATTTACAG[A/G]GAATGGGATGGCCAC | 50862 |
rs530718837 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10523735 | TTCTTCATTAAGAAG[A/T]CTGTAACAAGAAAAA | 50862 |
rs530799542 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10524251 | AAACCCCGTCTCTAC[C/T]AAAAATACAAAAAAT | 50862 |
rs530876305 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526187 | GACATAGGATGGAAG[A/C]CTGGGGAAGAAGTAA | 50862 |
rs530921688 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531936 | TCTACAGTTCTCGGA[A/G]ATCACTGCACGTCTG | 50862 |
rs530956599 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540056 | ATACTATTTTTGAGC[C/T]CTGAATTCAGAAAGC | 50862 |
rs530999078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519006 | CCACTGACCTTGGCC[C/T]AGCCCATGAATGCAG | 50862 |
rs531288792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540948 | CAATAGAATGGCCTC[C/T]CCAGCCGTCCCCACG | 50862 |
rs531301419 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511819 | TTTTAAAACAGCACA[C/T]AAACATCACAAGCCC | 50862 |
rs531321882 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541531 | TGGTTTGGTCAACAG[C/T]TGGGCTCCAAGGTAC | 50862 |
rs531383026 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519633 | ATAGTCTATTGCTTC[C/T]AGGCTACAAACATAT | 50862 |
rs531443003 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10539125 | ATGCCACATTCTCTA[A/G]TGGGTGGTACATAGT | 50862 |
rs531782168 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10534336 | TACATGAGTCTAAGG[C/T]AGAATTTAAATGACT | 50862 |
rs531782275 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10526985 | AACAGGCTTACAAAA[C/T]AGATCTTCAGAGCTG | 50862 |
rs531817475 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10533854 | TTAAAAAGCTACATA[C/G]AAAGTCAACTTATAA | 50862 |
rs532033046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520457 | TTCCGCCTCCACCTC[C/T]TGTCCCACTGGAAGG | 50862 |
rs532119589 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10518486 | TGAAAGAAGCCAGAC[A/C]AAAAAAGCACATATT | 50862 |
rs532132831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528813 | ACCGTATTACAGCCT[A/G]TAAGAGATACAATAA | 50862 |
rs532160129 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542918 | CCCAGGTGCTTATCA[A/G]TAGTGGATTGGATAA | 50862 |
rs532250482 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522654 | ACTGTTTTCAAATAT[C/T]TGAAAGGCTGGAAAA | 50862 |
rs532354223 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10537410 | ACCAGGCTGAAAACT[C/T]TGAATAATATCTACA | 50862 |
rs532715464 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10516679 | GCTTTGAGGGGATAG[C/T]CCCCTAAAGCTCACT | 50862 |
rs532923661 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511301 | GATTCTCAAGGAGCA[C/T]GAACTCTACTGTGAA | 50862 |
rs532927150 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511939 | TAGCTAAAATCACTT[A/G]CGAAAGATTATTTAT | 50862 |
rs532951325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10524297 | GCGGGCGCCTGTAGT[C/T]CCAGCTACTTGGGAG | 50862 |
rs533080905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517614 | ACAACCTTAAAAACA[C/G]AGGGAAAAAATGGCA | 50862 |
rs533171848 | snp | C/G | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539672 | AGAATCAAAGATCTT[C/G]ATCAGAAAAAGATAC | 50862 |
rs533198787 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532907 | TGGGATAACAGGAAA[A/C]CTGAGATTCAGAGAG | 50862 |
rs533332746 | in-del | -/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541549 | GCTCCAAGGTACCAC[-/T]TTCCCAGACCTCCAG | 50862 |
rs533354212 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10526268 | AAATATTTAGAAAGA[A/C]ATGAAGAATATAGGG | 50862 |
rs533431509 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512858 | TAATGTTTTTATTCA[C/T]TGACTTAATCACATT | 50862 |
rs533431897 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520164 | TACATTTAGGCTATA[C/T]GAAATTTATAAAAAA | 50862 |
rs533444612 | in-del | -/GTA | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518584 | GTACATTAAATACAT[-/GTA]GTTTATTGTATGTAT | 50862 |
rs533468663 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519743 | CAGAGAAGGTACTGT[A/G]TAAATACGGTATACA | 50862 |
rs533471063 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540728 | TCGCTCTGGCTACGC[C/G]GCCTCAGCCCCTCCT | 50862 |
rs533489809 | snp | A/C | | | intron-variant | RNF141 | GRCh38.p7 | 11:10515196 | GTGAAAAATAAATCC[A/C]TCCCTCCTATCTCAA | 50862 |
rs533506666 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526530 | GGCTCATGCTTGTAA[A/T]CCCAGCACTTTGGGA | 50862 |
rs533803634 | in-del | -/CA | 0.00199481 | 0.0315187 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540766 | ACCTGGACATTTAAC[-/CA]ACAGCTAAGTCCGGC | 50862 |
rs533830614 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541028 | CGGAAGCCTGGCTCG[A/G]CAGCGGAGGGCCCTC | 50862 |
rs533904169 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542327 | TGTGCACCATTATTT[C/T]CCTGACAGCCAGCAT | 50862 |
rs533940011 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541853 | TTAAGTCGTCTGGTC[A/G]AAGTTGCCTAGACAA | 50862 |
rs534125657 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513658 | ATTTTATGTATATAC[A/G]GTAAAAAAGCCTCAC | 50862 |
rs534155576 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520665 | GTAACATAATTATCA[A/G]GTATTACTGTACATA | 50862 |
rs534435971 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513231 | GTCTTCAGTATTTTT[A/G]GGGGCGAAATCAAGC | 50862 |
rs534574990 | in-del | -/AG | 0.00597247 | 0.0543191 | intron-variant | RNF141 | GRCh38.p7 | 11:10517613 | AACAACCTTAAAAAC[-/AG]AGGGAAAAAATGGCA | 50862 |
rs534595443 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516359 | CAAAGGACAGTGATC[C/T]CTGGGACATGGGAGT | 50862 |
rs534635929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515719 | GATATTATTAATTAT[C/T]TTTCTAAGAAATATC | 50862 |
rs534656838 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10523950 | TGTTCTAAAAGTCAC[A/T]TGGCCTATCAGTAAC | 50862 |
rs534771695 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521601 | AGTACTTAAAATTTT[G/T]ATTTGAATGTAAAAA | 50862 |
rs534772703 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528474 | ATCACATACAGATGT[C/T]AGACATATTGAGGCA | 50862 |
rs534826438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10524334 | GCAGGAGAATGGCGT[A/G]AACCCGGGAGGCAGA | 50862 |
rs534863603 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10535869 | TCGAATCCAAACTTA[C/T]GAAAACATCATCAGA | 50862 |
rs534875050 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536849 | CTCTTGCTAGAAGCA[G/T]GTATCTTGAGCAAGC | 50862 |
rs535053159 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539313 | GCAAAATGGAAAAGG[C/T]TGAAAATGCACCAAA | 50862 |
rs535123022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538769 | AGCAGAAGTTAAAAA[C/T]ATGTATGAAAGAAAA | 50862 |
rs535266414 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540004 | AAAAGTTCTAGAAAC[C/T]GAAGTCAGGCAATGT | 50862 |
rs535317424 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10537563 | GAGGTCTCCAGCTGG[C/G]CCCAAGAATTAAACT | 50862 |
rs535517662 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10531748 | ATCATTACTAACAAC[A/T]CTCTCTGAGCACCAG | 50862 |
rs535522905 | snp | A/G | 0.00676609 | 0.0577691 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512547 | AAGATCCAAAACTCT[A/G]TAAGGTAACTCTGTT | 50862 |
rs535632676 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10525932 | CGTTTAATATGAGGT[C/G]AAACCAGTGGCCCAA | 50862 |
rs535720231 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10532323 | TTGCACACTACCCTT[G/T]GGATAATTTTTAAAA | 50862 |
rs535781062 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10539209 | AAAATATTAAAATTA[C/T]ATCATGGGTAACTGG | 50862 |
rs535850672 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512957 | GTATGTGTGTATGCA[C/G]ACGTGTTTAAAGGTT | 50862 |
rs535897856 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527169 | ATGTTATTGGTACTA[G/T]GTGCACTGCTCTAGG | 50862 |
rs535944779 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513746 | GTGCAGTGGTGTGAT[C/T]TCGGCTCACTGCAAC | 50862 |
rs536161065 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10515669 | CTCTAGGAATAACTT[C/G]TTGGCAGTGGCAGGG | 50862 |
rs536178611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519237 | TTAAACATCTATATG[C/T]CCACAGTATAAAGCA | 50862 |
rs536201811 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10536076 | ACACAAATAAATGTA[A/T]AATTACAAAATGAGA | 50862 |
rs536236515 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10527788 | GAGAAGCAGGGAGAT[C/G]AGTTAGGAGGCTACT | 50862 |
rs536287371 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10543070 | CAGGAAACCAAATAC[C/T]GCATGTTCTCACTTA | 50862 |
rs536365153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536647 | AAAGAGATGGAGTCT[C/T]TTTAAACAAACAGAG | 50862 |
rs536368248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521363 | TTGTCTTAGATTCTC[A/G]ATAAATGCTTCTTGA | 50862 |
rs536494587 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541174 | TGCGCTGCCTCAGCC[C/G]ACAGCTCAGACCTGC | 50862 |
rs536527514 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542383 | TGATGAATATTTGAA[C/T]ACTGGAAAAGGAAAA | 50862 |
rs536733306 | in-del | -/TTAACA | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10528217 | TTTTTTTAAAGTTGT[-/TTAACA]TTAAGAAATGTGAAA | 50862 |
rs536875409 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522374 | TAGCCAGTGGAACCA[C/G]TACAAAGTTCTCTTA | 50862 |
rs537043898 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10525071 | TGATCTCAGATACAA[C/T]ACCAACTGAGAAAAA | 50862 |
rs537265995 | in-del | -/C | 0.0111196 | 0.0737302 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540458 | AAGCTAACACAGAAG[-/C]CTTCTGCTCCTGCTG | 50862 |
rs537399564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532424 | GTAAAATGTAAAATC[G/T]CCCTCTCTGCCCCCT | 50862 |
rs537483568 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540499 | ACCTTCTTATTATTA[A/G]CAAGAAAACGTTCTT | 50862 |
rs537484028 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10524364 | AGCTTGCAGTGAGCC[A/G]AGATCGCGCCTGGGC | 50862 |
rs537593037 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10529982 | CGGGAATGAACTTCA[C/G]AGCGCTCATGAATGC | 50862 |
rs537596920 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538450 | AGTGCATGTTCACGA[A/T]AACAATCTGTTGAGG | 50862 |
rs537682106 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10537710 | TACATAGTAGATTGG[A/T]CAAAGGAGAAGTAAA | 50862 |
rs537789975 | in-del | -/AC | 0.483335 | 0.089748 | intron-variant | RNF141 | GRCh38.p7 | 11:10532497 | TTTAGTTCATTTTCT[-/AC]ACACACACACACACA | 50862 |
rs538048209 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519962 | TAACACTAACACTAA[C/T]AATATCTGATGAGCT | 50862 |
rs538074296 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526492 | ACTGAGACTCAAGAA[G/T]GAGTCATGCGGCCAG | 50862 |
rs538247424 | snp | C/T | 0.00199481 | 0.0315187 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514842 | GTGTCTGTGCCAGTG[C/T]CACAACCCTACATTC | 50862 |
rs538284486 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521546 | AATATGTTTTCCATT[A/C]CCTGTTGTGCTTATA | 50862 |
rs538419917 | in-del | -/A | 0.00318978 | 0.0398085 | intron-variant | RNF141 | GRCh38.p7 | 11:10529451 | GAAGCACTGAACTGG[-/A]AAAAGAAAAGTAACA | 50862 |
rs538462218 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519369 | AAAGACTAGATAAAA[G/T]ATACATTTTGTGATA | 50862 |
rs538494385 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513529 | TGAGGTGCAACTGAA[A/G]ATCACAATTCCATTA | 50862 |
rs538732909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515582 | AGAGGAAATTCCCTC[A/G]CATCAATGGAAGATT | 50862 |
rs538949027 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536163 | TAGTTTTGTATCAGG[A/G]AAGAAGTCCCTGGGC | 50862 |
rs538949524 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527865 | GTAGCGTAGATGGTG[A/G]GAGCTAGCCAGATTC | 50862 |
rs539071399 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10536710 | CTCAAGCAATCCTCC[A/C]GCCTCGGCCTCCCAG | 50862 |
rs539275872 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10523918 | ACAGGAAAGACAAGC[A/C]TAAACACTGCCTACC | 50862 |
rs539289325 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516446 | CTGATCAAGAAGCGG[A/G]AAGCTTGATGGAACA | 50862 |
rs539605648 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531421 | TATCAAAATTTTTTG[A/G]CTGTTGCCTCAGACG | 50862 |
rs539799586 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519559 | CTGTGTAAATATCAT[A/G]GTGTACTTATACAAA | 50862 |
rs539875261 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520433 | GTCAGGATCACCACC[A/G]TCACTGTCTTCCGCC | 50862 |
rs539890513 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10526109 | TGAAGGTATAATGTT[C/T]TTGGATGAAGAACTT | 50862 |
rs539973650 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512639 | AAGGACAATTTAAAA[C/T]CTTAGAGCTGGAAAA | 50862 |
rs539999821 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10524405 | GACTCCGCCTCAATT[A/G]AAAAAAAAAAAATCA | 50862 |
rs540119049 | snp | C/T | 8.96435e-05 | 0.0066943 | intron-variant | RNF141 | GRCh38.p7 | 11:10525392 | AAAATACAAAGAACA[C/T]GAAAAAGAAAAGTTG | 50862 |
rs540134174 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542990 | ACAAAAAGGACTAGA[A/T]CATATCTTTTGCAGC | 50862 |
rs540206529 | snp | G/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514417 | CCACAAGGGGGCATA[G/T]ATATATATACTCCTT | 50862 |
rs540466959 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10519236 | ATTAAACATCTATAT[G/T]CCCACAGTATAAAGC | 50862 |
rs540716764 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10520298 | ACACACATTATACAG[C/T]TGTACAGAAATATTT | 50862 |
rs540749643 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10535531 | TGGATTTACAGCAAC[G/T]GTATCCAAGAAGAAA | 50862 |
rs540953891 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540748 | CAGCCCCTCCTCAAG[C/T]GCACCTGGACATTTA | 50862 |
rs540987545 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10516589 | TACGGAAGTGTCCCC[A/G]CCAGAATACTCAGCA | 50862 |
rs540994372 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542655 | TGGAATACTACAAAA[A/G]AGCTGCTAGAACTCA | 50862 |
rs541075300 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10515991 | CCGTATTTGAGCCAG[A/G]GACATATTATGCAGA | 50862 |
rs541310920 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522536 | ACAGAGAAAAGACCA[C/T]CTGGGAAAGCCTCCA | 50862 |
rs541353675 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518038 | AAAGAAGACCTAAAT[A/G]AGTGGAGAAATATAC | 50862 |
rs541361039 | snp | C/T | 0.000358603 | 0.0133856 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514902 | AATAGCAACAGAAGA[C/T]TTTCACTTCAAGGTC | 50862 |
rs541383209 | in-del | -/CTA | | | cds-indel | RNF141 | GRCh38.p7 | 11:10513311 | TCGCCTATTAAAATC[-/CTA]CTATCCAGAAATTCT | 50862 |
rs541415681 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10531119 | CAGTGGCTCACACCT[C/G]TAATCCCAGCACTTT | 50862 |
rs541553107 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10524310 | GTCCCAGCTACTTGG[A/G]AGGCTGAGGCAGGAG | 50862 |
rs541584932 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10528757 | TCAACAGATTTTTTT[G/T]GTTCACTTAATATAT | 50862 |
rs541611359 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10525660 | GACTTTCTCAGAGTT[A/G]AGAAATAAATTTTAG | 50862 |
rs541621575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536283 | GGTTATGAAAAGTGC[C/T]TGAGACAGGAAGCAG | 50862 |
rs541732475 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532318 | ATGCTTTGCACACTA[C/G]CCTTTGGATAATTTT | 50862 |
rs541745022 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10527508 | GAGTCTCACAAGAAG[C/G]CCAGAGTGTTTGGAA | 50862 |
rs541763615 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | RNF141 | GRCh38.p7 | 11:10524240 | CTAACACGGTGAAAC[C/T]CCGTCTCTACTAAAA | 50862 |
rs541960447 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517460 | AAATCTGAAAAAATA[A/G]TGGCTGAAAAATTTC | 50862 |
rs542211780 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539955 | ACCAAATGACAAATA[C/T]TAATTTTTGAAACAT | 50862 |
rs542240553 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512765 | TGAATTTAATTAAAA[A/C]ATTTTTTTAAAAAAA | 50862 |
rs542289832 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531903 | TAGCTGCCAAGCTTC[A/G]TCCTGTATAGGTTTA | 50862 |
rs542526620 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519593 | AGATGGTTTAGCCTA[C/T]TACTACATACCTAGG | 50862 |
rs542562597 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511720 | CCCAATGTTAAAAAT[C/G]ACTGAATCAAAAGAT | 50862 |
rs542611958 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521108 | AAAAAGATTTCAAAC[C/G]TTTTGCTCCAGCCAC | 50862 |
rs542655692 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10535219 | AAAAAATAAAGCTAT[A/G]AATTTAAAATATATA | 50862 |
rs542776440 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10533835 | CTGTCCCCATTACAT[A/C]CTTTTAAAAAGCTAC | 50862 |
rs542776685 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541928 | CTGCCTCTATGCTTA[A/G]CAGTTAAACTGGTTT | 50862 |
rs542886519 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10532765 | GTTGTAATGCCTACG[C/G]AGTGGGTTCATATAT | 50862 |
rs542890758 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10534312 | CTTTAAGTGAGAGTT[A/G]AGTAGACCTACATGA | 50862 |
rs542964830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527950 | AAAGAAAAGCCAAGA[A/G]TGACTCTAAGAAGTT | 50862 |
rs543120402 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521762 | AACAAAGTTGTAGAG[A/G]TAAAAAGCAAAATCA | 50862 |
rs543449377 | in-del | -/GGCTACTGTAGGCTACTGTAACACTGTAGCCTACAC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10519664 | TAGCATGTTACTGTA[lengthTooLong]TGGAACACTGTAGGC | 50862 |
rs543482278 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517191 | ATGAAAGATAATAAA[A/G]ACCCAAATCAAACTT | 50862 |
rs543506611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10523521 | ACATCAATGGAATTA[C/T]GCATCAGATGTAAAG | 50862 |
rs543519859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528786 | ATACTGAGTTCCTAC[C/T]ATGTGTAAAGCACCG | 50862 |
rs543629573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515756 | ACTTTCAACAATATA[G/T]CTACCTGTTGCTTGC | 50862 |
rs543668283 | snp | C/T | 5.00705e-05 | 0.00500327 | intron-variant | RNF141 | GRCh38.p7 | 11:10515095 | CAAAACAAAACAGTT[C/T]GCTTTCTTCTTTTTT | 50862 |
rs543772071 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10524038 | AATAAATGGAAAATA[A/C]AGTTTAACTGTAACA | 50862 |
rs543844583 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531779 | TGGGGATATCACACT[C/T]AACTAACAGCTAAAT | 50862 |
rs543895014 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10535296 | GGTATTAAAATTTAA[C/T]GTACTGTATTTGAAG | 50862 |
rs543988656 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10518722 | CTAAACACATACACA[A/G]AATAAATGTAGAAAT | 50862 |
rs544004257 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538125 | TTGTTTCAGCATTGT[G/T]TTCATCTGCTGCCCT | 50862 |
rs544148766 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | RNF141 | GRCh38.p7 | 11:10518263 | CACCCAAGAAAAAAA[A/C]CAAAATACATCCATA | 50862 |
rs544234938 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10524814 | AATTAGACATTTTTT[A/T]AAAAAAGTGGGATGA | 50862 |
rs544291665 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540696 | GCGGAGACCGAGCCC[C/G/T]CGGGCCACCCTAGCG | 50862 |
rs544327976 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10536912 | AGGCCACACTGAAAA[C/G]TCTGTATTCAGCTCT | 50862 |
rs544568557 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541366 | GACGAGAGGTGGCGG[C/T]GAAGGAGAGTCTCGC | 50862 |
rs544589749 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532864 | GTCGATTTCATTCAG[A/C]CTTTTTAGGGTTTAA | 50862 |
rs544702140 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526190 | ATAGGATGGAAGACT[A/G]GGGAAGAAGTAAGCC | 50862 |
rs544830525 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520136 | CAGTAGTGTACAGAC[G/T]TTATGAACACTGTAC | 50862 |
rs544961342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522439 | GAAGGAAGGAGAGTC[C/T]TGTGCTGTTTGTTCC | 50862 |
rs545065858 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10526873 | AAATTTTGGGAAGGT[-/A]AAAATCTATCTGGAG | 50862 |
rs545241182 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512672 | TTTCAGTGGATCATC[C/T]ATCCCAAGGTTTTCA | 50862 |
rs545284483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10534365 | CTCTGTTTTCAGATT[C/T]ACATAGCTAAATGAG | 50862 |
rs545305192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520896 | GGTGATACATGACCA[C/T]ATAATTTATTCACTA | 50862 |
rs545436333 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10535291 | CTTTAGGTATTAAAA[A/T]TTAATGTACTGTATT | 50862 |
rs545505515 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515868 | AACTTTACATGCACA[C/G]TAATTTTTCTGGCAG | 50862 |
rs545593674 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542410 | AAAAAGCTTAAAAAT[A/G]AAGTATAAATAATGA | 50862 |
rs545789493 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10529242 | AGGGGATATGACCCA[A/C/G]TACTGACCAGTGAGT | 50862 |
rs545901450 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10530151 | TCTGAATCTACTCAG[C/T]GGTGGTTGAGGCTTT | 50862 |
rs546205730 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10533017 | TACTATGTGCTTAGT[A/G]AATGTTAGCTAAGTT | 50862 |
rs546275322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538876 | ATACTCCCCCCTAGG[C/T]CATGCAACAGTGGTA | 50862 |
rs546361859 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10517688 | AACAATGCAAACAAG[A/G]TGAGTGTGAAGCAAC | 50862 |
rs546398211 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10524332 | AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA | 50862 |
rs546667762 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | RNF141 | GRCh38.p7 | 11:10539230 | GGGTAACTGGCAAAG[C/G]AAAAACGAAAAAACT | 50862 |
rs546763491 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512862 | GTTTTTATTCATTGA[C/T]TTAATCACATTTATA | 50862 |
rs546806046 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10528474 | TCACATACAGATGTT[-/A]AGACATATTGAGGCA | 50862 |
rs546883785 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540252 | AAGAATTATAAACAA[A/C/T]TGAAAGTGTTCCAGC | 50862 |
rs546989070 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10519751 | GTACTGTGTAAATAC[A/G]GTATACAAGATTAAA | 50862 |
rs547026368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526311 | ACACAGGGCCATAAA[A/G]TTGTGACTTTAGGTT | 50862 |
rs547267687 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532925 | GAGATTCAGAGAGGT[A/G]GACATGCCATTAATA | 50862 |
rs547309258 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10525780 | TACAACTCAAACAAG[C/T]ACTTTCTTAAATATC | 50862 |
rs547336915 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10534506 | CACACACACACACGC[A/G]TTCAAGTAATTGTAT | 50862 |
rs547422854 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542081 | TAAGGACTTTAAAGG[C/T]ATTAATTCGTTTAAT | 50862 |
rs547448582 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527755 | TTGTTGTGCTGAGAA[C/T]AGACAGAAGCAGGGC | 50862 |
rs547617673 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513358 | GCAACTTAAATTGTG[C/T]ACCCTGGTTTAGGAA | 50862 |
rs547684706 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10522089 | GGTCTAAGAAGCATT[A/G]TAAAAGACAAATCTT | 50862 |
rs547812647 | in-del | -/ACACACAC | | | intron-variant | RNF141 | GRCh38.p7 | 11:10532531 | CACACACACACACAC[-/ACACACAC]CCCACAACTATATAC | 50862 |
rs547830748 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10530838 | AGATTCAAGAAACAA[C/T]TTCAGAGAAGGAAAT | 50862 |
rs547985171 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536513 | ACAGACACTTACATG[C/T]TATTTAATATGACTA | 50862 |
rs547993942 | snp | G/T | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542342 | CCCTGACAGCCAGCA[G/T]GGTACTTGTTCAATA | 50862 |
rs548245615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516360 | AAAGGACAGTGATCC[C/T]TGGGACATGGGAGTC | 50862 |
rs548334947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528902 | CTAAACAACTTTTTT[C/T]GTAATGCAGTATTAT | 50862 |
rs548480628 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522817 | TTATGTCTTTTAATT[A/C]TCTCAAAAATCCTAT | 50862 |
rs548527068 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10524338 | GAGAATGGCGTGAAC[C/T]CGGGAGGCAGAGCTT | 50862 |
rs548658968 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540848 | AGAAGGAAAAACTCT[A/C]TCCGGGTCCCTCAGA | 50862 |
rs548659117 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532329 | ACTACCCTTTGGATA[A/G]TTTTTAAAAATAAGT | 50862 |
rs548694023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540486 | CTGTGTAATCACTAC[C/T]TTCTTATTATTAGCA | 50862 |
rs548720283 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511338 | ATACGAGGGATCTAG[A/G]TTGCATGCACCTTAT | 50862 |
rs548802919 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10518443 | TACATGCTACAACAT[G/T]AATAAATACCAAGGT | 50862 |
rs548878351 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512056 | TCAAACTAAGGTTCT[A/T]TACATAATCGGAGTA | 50862 |
rs548947105 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540013 | AGAAACTGAAGTCAG[C/G]CAATGTGAAAGAAAA | 50862 |
rs548982484 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10538302 | TTTTCAACCTGGTTC[C/T]AGAAAGAGGGCTTGA | 50862 |
rs549015637 | in-del | -/A | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518000 | GCAACACTGAAAACT[-/A]AAAAAAATTGGTGAC | 50862 |
rs549062234 | in-del | -/ATAG | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539598 | TCAAGACAAGTTAAT[-/ATAG]ATACATAGTGAAATA | 50862 |
rs549163161 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | RNF141 | GRCh38.p7 | 11:10522019 | TGAGGGACAGTCTAG[-/A]AAAGAGGAAAACTGG | 50862 |
rs549273931 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10526435 | TAATAGTTGTAACAC[A/G]TTTATTAATTGCTTA | 50862 |
rs549392197 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10519913 | TTCCCTGGGCCACAC[G/T]GGAAGAACTGTCTTT | 50862 |
rs549401187 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520423 | CCTAAACAGCGTCAG[G/T]ATCACCACCATCACT | 50862 |
rs549402261 | in-del | -/C | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540452 | TTTCAAAAGCTAACA[-/C]AGAAGCCTTCTGCTC | 50862 |
rs549443382 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512964 | TGTATGCACACGTGT[C/T]TAAAGGTTCTGTAAG | 50862 |
rs549477741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10521416 | CTTTGTGCTTTTTTG[C/T]AATTTTTAAGGTTTT | 50862 |
rs549512880 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514339 | GTTCCAAAACACACT[G/T]CTAAAGTTATGAAAT | 50862 |
rs549575729 | snp | A/G | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539742 | AAAGGATAGAGTGCC[A/G]TACTAGGAGATTAAG | 50862 |
rs549627902 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10526790 | ACGTCTCAAAAAAAA[A/G]AAAAAAGAATGAGTC | 50862 |
rs549795055 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542867 | TGTATACTGAAAACT[A/C]TAAAATATTATGGAA | 50862 |
rs549804508 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10535645 | AAGCACCATGGTGTT[G/T]GATACTTCTTTTAAT | 50862 |
rs549828048 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10522157 | AGGGAAAAGAGGGAA[A/G]TCACTGAATTGGAAT | 50862 |
rs549860014 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10529022 | GACCTTTAAAGAGAC[A/G]TCAGGTTTAGAGATG | 50862 |
rs549898980 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536681 | GTTGCCCAGTCTGGT[A/T]ACAAACTCCTGGGCT | 50862 |
rs549969135 | in-del | -/AAAC | 0.00080032 | 0.019988 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514294 | TATACAGTATGGCAA[-/AAAC]AAACAAACAAACCTT | 50862 |
rs550024606 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541680 | AAAAGTAATTACAAG[G/T]TTCAAAATCCTGAGC | 50862 |
rs550062788 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10516149 | CTGGCATATATTATT[C/T]AGGTTGATTTCTAGT | 50862 |
rs550126033 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542203 | CATTAAGGAGCAGAG[A/C]CAGATTCAAACCCAA | 50862 |
rs550149395 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10522571 | GTAGACGAGACCCAC[A/G]TAAACAAAGGCCAAA | 50862 |
rs550325612 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | RNF141 | GRCh38.p7 | 11:10530538 | GTTTTACAAAACCAC[C/T]GAGTTATTAAAATGT | 50862 |
rs550346776 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10517541 | CAAGCACAAGAAACA[C/T]GAAAAAACTACTCTA | 50862 |
rs550349755 | snp | C/G/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512920 | TTTATAATAATATGA[C/G/T]TTTTATATAGTGGGG | 50862 |
rs550408251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10530943 | GAACATAAACATGCA[A/G]CTTAATTTCTAAGGT | 50862 |
rs550711377 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511232 | GAGTTGAGCCGCGGG[C/T]GAGTGAGTATTATTG | 50862 |
rs551005275 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10525130 | ACAGCAAAAATATTA[A/G]TAGATTTCAGTTGTT | 50862 |
rs551213174 | snp | C/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512095 | GTTACTGAGTTAGGA[C/T]AGGGAAAACAAATTC | 50862 |
rs551262047 | snp | C/T | | | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539427 | CCTAAAAGGATTTAA[C/T]TGAAATAAACATCAA | 50862 |
rs551295783 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10531322 | GAAGGTTGTAGTGAG[C/T]CAAGATCACGCCATT | 50862 |
rs551333135 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512193 | ACATTTAAGTACTTC[A/G]TATTTAAAAAAGACA | 50862 |
rs551367894 | snp | C/T | | | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542302 | CATTAGCGCTAGGTC[C/T]ATGCCTGTTTGTGCA | 50862 |
rs551511735 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512789 | AAAAAAAACGACTCC[A/C]ACTATATGTGTGTTA | 50862 |
rs551541666 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10520253 | TACTTTTAACTTTTT[C/G]ACTCTTTTTGTAACA | 50862 |
rs551541707 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10542282 | TCGGTAGTACGGTAA[A/G]ACTTCATTAGCGCTA | 50862 |
rs551559633 | snp | G/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10515918 | TCACTTAAATAAGAT[G/T]ATGTTTTCGAAAAGG | 50862 |
rs551598428 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519640 | ATTGCTTCTAGGCTA[C/T]AAACATATATAGCAT | 50862 |
rs551769264 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513585 | AATGGAAAGAGTATT[C/T]CAATGGAAGTACAGT | 50862 |
rs551797128 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514422 | AGGGGGCATATATAT[A/C]TATACTCCTTAGATT | 50862 |
rs551906052 | in-del | -/TCT | 0.00517822 | 0.0506191 | intron-variant | RNF141 | GRCh38.p7 | 11:10526612 | CACGGTGAAACCCCA[-/TCT]CTACTAAAAGTACAA | 50862 |
rs552032998 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521211 | AGTTTAGTAAGCTCC[A/T]ACCTTGGTAACTCAG | 50862 |
rs552213695 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522197 | GAATAAAAACCTAGA[C/T]GGATATGGGTCTAAT | 50862 |
rs552235793 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10516264 | TCCAACCAACAGAGG[A/C]TAGATTTATCTTCCC | 50862 |
rs552289907 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10526760 | GCACTCCAGCCTGGG[C/T]GACAGAGCAAGACTA | 50862 |
rs552494415 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528401 | AAAATATCTAATTGC[C/G]TGTGCCTTTAGTACT | 50862 |
rs552823467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538741 | GTCATCTATTAGTAC[C/T]AGGTTGGAGAGAAGC | 50862 |
rs552949031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10537859 | ATTGCCCACTTCTAG[C/T]AATGATAATGTCTTC | 50862 |
rs553073999 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10537304 | TGGAGTAGGTGACCT[C/T]TAACCTAACATTTTA | 50862 |
rs553304702 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512252 | TTTCATCCATTAAAC[A/C]AATTTACAACTTTTA | 50862 |
rs553427622 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513249 | GGCGAAATCAAGCTA[A/C]CCCTGGCCAGATGTT | 50862 |
rs553427843 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520696 | ATTGTAAGTGCTATA[C/T]TTTTATACTATGAGC | 50862 |
rs553535706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531439 | GTTGCCTCAGACGTA[C/T]ATAAAGCATGAAAAA | 50862 |
rs553571231 | snp | A/G | 1.67175e-05 | 0.0028911 | splice-donor-variant | RNF141 | GRCh38.p7 | 11:10525190 | ACTTATGCATTATAT[A/G]CCTTCCCATCCAAAG | 50862 |
rs553733547 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10526554 | TTTGGGAGGCCGAGG[C/T]GGGCAGATCATGAGG | 50862 |
rs553764776 | snp | G/T | | | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10514540 | TACAACTTTTTAATA[G/T]TCGAGGTTTATTTTA | 50862 |
rs553812024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10532686 | CTTCACATAAAGACA[A/G]TATATCAAGCTTATC | 50862 |
rs553893131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10534260 | AAAAACGGCAATATA[C/T]TCATTCTTCAAAAAC | 50862 |
rs553982204 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523826 | CAGCTTTTAAAACAA[C/T]TAAACAAAACAACAA | 50862 |
rs554027303 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10533364 | AGGTGTACTCTTTAA[A/G]AAGGCAGAGAAATTT | 50862 |
rs554109276 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10517038 | GAAAAATATAATCTA[C/T]AATAAAGAGAAAAAT | 50862 |
rs554268200 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10535094 | TTATTTATCCATCAA[A/C]GACTATCATTTTATT | 50862 |
rs554415204 | in-del | -/G | 0.136775 | 0.22289 | intron-variant | RNF141 | GRCh38.p7 | 11:10527646 | GCATGAGAAGTCACG[-/G]GGGGGGGGTTTTGAG | 50862 |
rs554473696 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528545 | GTATTTGTCAAAGAG[C/T]AACAAAAAACGAAGG | 50862 |
rs554477256 | snp | A/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10518765 | AGGAGGAAAAAGGGA[A/T]ATGTTTGATTTTAGA | 50862 |
rs554625338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517784 | TGAAAAATGATATTC[A/G]GACATTCAAGAAGAG | 50862 |
rs554768076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522327 | AAAGAAGAGCATTGT[A/G]GAGAGAGATAAAAGA | 50862 |
rs554772374 | snp | C/T | 0.000659348 | 0.0181449 | missense | RNF141 | GRCh38.p7 | 11:10515041 | TCTGTAGGCGACAAA[C/T]AGGGCAATTCCTGTG | 50862 |
rs554806092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520731 | CAGTAGGTTTGTTTA[C/T]ACCAGCATCACCAAG | 50862 |
rs554809241 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10521734 | TTTTAATAGAAGACA[C/T]TCTAGGTGCATAAAC | 50862 |
rs554956535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10539352 | ATGACAAGTACTGCA[C/T]TGTAGTATTTTAAAA | 50862 |
rs555069650 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10531755 | CTAACAACTCTCTCT[C/G]AGCACCAGTGGGGAT | 50862 |
rs555214215 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10536876 | AAGCAGCCTACTAGT[C/G]CATTATGCTTTGCAA | 50862 |
rs555613816 | snp | A/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10537988 | TTCAATGTGCTTTTA[A/T]CTCAAAATAATCCTT | 50862 |
rs555711341 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513753 | GGTGTGATCTCGGCT[C/G]ACTGCAACCTCCACC | 50862 |
rs555929590 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10526003 | TTACAATCTAATGTA[C/G]AAGATACTTGGGGCA | 50862 |
rs555946943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540644 | TTTCTGAGCTATCGT[C/T]CCAGGCAAAAGGTTT | 50862 |
rs556073878 | snp | G/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10512357 | AAGAGCTGTGCTCAT[G/T]TATTTATTTGATAAG | 50862 |
rs556132712 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10520821 | AGGAATTTTTTAGCT[A/C/T]CATTATAATCTTGAG | 50862 |
rs556219598 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | RNF141 | GRCh38.p7 | 11:10526615 | GGTGAAACCCCATCT[C/G]TACTAAAAGTACAAA | 50862 |
rs556275256 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10528655 | ATGAAATAAAAATGA[A/C]CATTAAGTGTAATTT | 50862 |
rs556333565 | snp | C/T | | | missense | RNF141 | GRCh38.p7 | 11:10525361 | CCTCCACAATGCCAC[C/T]GCTTTTGTTAATCTA | 50862 |
rs556402185 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | RNF141 | GRCh38.p7 | 11:10535222 | AAATAAAGCTATAAA[A/T]TTAAAATATATATAA | 50862 |
rs556416004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10533381 | AGGCAGAGAAATTTA[C/T]ATTTCATTTTAGAAA | 50862 |
rs556421084 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527176 | TGGTACTATGTGCAC[A/T]GCTCTAGGCACTAGC | 50862 |
rs556802741 | snp | C/T | | | intron-variant | RNF141 | GRCh38.p7 | 11:10528097 | CATTTAAACATAATT[C/T]AGATCATTTTTTATA | 50862 |
rs556849590 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516430 | CGAGAGTTTCTAGCC[C/T]CTGATCAAGAAGCGG | 50862 |
rs556888169 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10522962 | TGCTGCTAGAGTCTG[C/T]GCCGTGCTGCCTCAA | 50862 |
rs557052481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10537722 | TGGACAAAGGAGAAG[A/T]AAACTGTGAAAACAT | 50862 |
rs557085900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10517885 | ATATACAAATATCTA[C/T]TGTATTTCCATATAC | 50862 |
rs557127562 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515774 | ACCTGTTGCTTGCTT[A/C]AAGGTCTGAAAAAAT | 50862 |
rs557350894 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10532476 | AGAGACAAGCACTGG[A/G]AATAGTTTAGTTCAT | 50862 |
rs557409331 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | RNF141 | GRCh38.p7 | 11:10511475 | CCTGGTGCCAAAAAG[G/T]TTGAGGACTGCTACA | 50862 |
rs557554205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10538500 | CACAGCTTTTCAGTG[C/T]CCCTCTTTGGTGACT | 50862 |
rs557611946 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10530022 | GGTTTATATGCATAT[A/G]GATGATTTTGTTCTT | 50862 |
rs557722386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10530865 | AAATATGAAGAAACA[C/T]AAAAAGACAAATAAT | 50862 |
rs557848622 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, nc-transcript-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10541373 | GGTGGCGGCGAAGGA[C/G]AGTCTCGCCTGTCAC | 50862 |
rs557961369 | in-del | -/G | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540454 | TCAAAAGCTAACACA[-/G]AAGCCTTCTGCTCCT | 50862 |
rs557991418 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10540543 | CTCAAGGTAGCAGCT[A/T]GTTTGACAAGGAAAG | 50862 |
rs558174480 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | RNF141 | GRCh38.p7 | 11:10521138 | CAATTCAGAGAGCCC[A/C]TGAATGAGCCATATA | 50862 |
rs558241006 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10515584 | AGGAAATTCCCTCGC[A/G]TCAATGGAAGATTTG | 50862 |
rs558300739 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10513056 | TTCTAAAGTAAGAAC[A/G]CATAAACAAGAGTAA | 50862 |
rs558342296 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519989 | AGCTAAAAAAATTGC[A/C]AAAAAATCTCATGTT | 50862 |
rs558361406 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10523118 | TTGTACTTGCAAGTC[A/G]GACTTGGCAAAATGT | 50862 |
rs558659622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10523188 | ATCAGCAGCATTGGC[C/T]CCACCTGGGAGCTTG | 50862 |
rs558807979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527317 | TGGAGAAGATGAAAC[A/T]GGGGAGAAGGAACGC | 50862 |
rs558889819 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10521548 | TATGTTTTCCATTCC[C/T]TGTTGTGCTTATAGC | 50862 |
rs558925377 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10527874 | ATGGTGAGAGCTAGC[A/C]AGATTCTGAATACAT | 50862 |
rs558943048 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536728 | CTCGGCCTCCCAGGC[C/T]GAGGATTACAGGCAT | 50862 |
rs559007235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516576 | AATTCCAGAGGTCTA[C/T]GGAAGTGTCCCCGCC | 50862 |
rs559123080 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | RNF141, MRVI1-AS1 | GRCh38.p7 | 11:10543220 | ATCATTAGAAGCCTA[A/C]ACCTCAGCATTGTTC | 50862 |
rs559204196 | snp | C/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10522010 | GAGTGCAGTATGAGG[C/G]ACAGTCTAGAAAGAG | 50862 |
rs559222342 | snp | A/G | | | intron-variant | RNF141 | GRCh38.p7 | 11:10531933 | AATTCTACAGTTCTC[A/G]GAGATCACTGCACGT | 50862 |
rs559231749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536191 | GGCAAACAACATTTT[A/G]CTTGAGGTCAGAATG | 50862 |
rs559314592 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | RNF141 | GRCh38.p7 | 11:10529164 | ATGCAGGAGTCAATC[C/G]TGGTTAGTCTAATCT | 50862 |
rs559479212 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10516740 | AGACTGGAAAACCTC[A/G]TAACTCTTGGGGTAT | 50862 |
rs559520142 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10523515 | TGTAAAACATCAATG[C/G]AATTATGCATCAGAT | 50862 |
rs559594300 | in-del | -/T | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10519952 | CATATATACTAACAC[-/T]TAACACTAACAATAT | 50862 |
rs559641192 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10536421 | ATGACCTGAAGACTG[C/T]ATGCCTGCCCAATCT | 50862 |
rs559718155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | RNF141 | GRCh38.p7 | 11:10519575 | GTGTACTTATACAAA[C/T]CTAGATGGTTTAGCC | 50862 |
rs559894837 | snp | A/C | 0.000399281 | 0.0141238 | utr-variant-3-prime | RNF141 | GRCh38.p7 | 11:10511959 | AGATTATTTATTGCA[A/C]AATTTATCAGTGGGT | 50862 |
rs559899128 | in-del | -/TGGAATAGGCTGGTTGTTGTGCT | 0.00119737 | 0.0244387 | intron-variant | RNF141 | GRCh38.p7 | 11:10527704 | TTTCAAATTGTGATG[-/TGGAATAGGCTGGTTGTTGTGCT]TGGAATAGACTGCTT | 50862 |