SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs901954 | snp | A/T | 0.494896 | 0.0502606 | intron-variant | NSMAF | GRCh38.p7 | 8:58613180 | ttaaaaatactaaaa[A/T]atatttttaatactt | 8439 |
rs931396 | snp | A/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58587448 | TTAGGTTTCCAAGTC[A/T]ACTTTGTTTTGTTTT | 8439 |
rs973807 | snp | C/T | 0.499713 | 0.0119774 | intron-variant | NSMAF | GRCh38.p7 | 8:58658728 | TGTCACCAAAAATGC[C/T]CTGGGAACTATACAT | 8439 |
rs1050488 | snp | C/T | 0.393987 | 0.204372 | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58583931 | AAAGCCATTAGTTGC[C/T]ATTCTCTTAGGGCAG | 8439 |
rs1050504 | snp | A/G | 0.3744 | 0.216852 | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58583857 | CAGATGATCGTCCCC[A/G]TATGATGATTGTCAG | 8439 |
rs1352496 | snp | C/G | 0.368119 | 0.220336 | intron-variant | NSMAF | GRCh38.p7 | 8:58636433 | GTACCCGTGTACTAC[C/G]TCTGAAAGTATTCTT | 8439 |
rs1387222 | snp | A/T | 0.435407 | 0.167703 | intron-variant | NSMAF | GRCh38.p7 | 8:58643172 | TGTTTGTTAAATTCA[A/T]GAATGGAAAAGCTTT | 8439 |
rs2054900 | snp | A/G | 0.147991 | 0.228242 | intron-variant | NSMAF | GRCh38.p7 | 8:58601976 | TTCCCCTAAGCCTTG[A/G]AGAAACGAATTTCCT | 8439 |
rs2130072 | snp | C/T | 0.372592 | 0.217879 | intron-variant | NSMAF | GRCh38.p7 | 8:58614140 | tcacaacatatgagg[C/T]gggaaattaaagaaa | 8439 |
rs2228505 | snp | A/G/T | 0.0621084 | 0.164914 | missense | NSMAF | GRCh38.p7 | 8:58595575 | AGTTACACGAGCACT[A/G/T]TAAAATCCACAAAGA | 8439 |
rs2228506 | snp | A/G/T | 0.000164786 | 0.00907584 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58597514 | GGTAGCCATGCTTAC[A/G/T]CAAATCTTGGAATTT | 8439 |
rs2229740 | snp | A/G/T | 0.00694917 | 0.0585432 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58589470 | GCTATATTCTGCATC[A/G/T]TGGGACTCTACAGTG | 8439 |
rs2242344 | snp | G/T | 0.486595 | 0.0807641 | intron-variant | NSMAF | GRCh38.p7 | 8:58658989 | GAATCAGGCCTTTCC[G/T]GCGGCCCCCCTCCCA | 8439 |
rs2255834 | snp | A/G | 0.496783 | 0.0399767 | intron-variant | NSMAF | GRCh38.p7 | 8:58603197 | TGGTCAGAATTCCAC[A/G]TGTGGCAGTTACCTA | 8439 |
rs2279459 | snp | C/G | 0.152001 | 0.229992 | intron-variant | NSMAF | GRCh38.p7 | 8:58595874 | AAGTATAAAAAGATT[C/G]TAGTATTATTCAAAG | 8439 |
rs2279460 | snp | A/G | 0.491783 | 0.0635686 | intron-variant | NSMAF | GRCh38.p7 | 8:58595816 | TTTTCCTTGACTAAC[A/G]TGGAACCATCTAACA | 8439 |
rs2279462 | snp | G/T | 0.491421 | 0.0649309 | intron-variant | NSMAF | GRCh38.p7 | 8:58595391 | ATCTCCACCTGAGGT[G/T]GATGTAGTAGGGAAA | 8439 |
rs2326129 | snp | C/T | 0.499539 | 0.0151687 | intron-variant | NSMAF | GRCh38.p7 | 8:58611978 | TCTCTGCTCCCAGTT[C/T]GTGGCACAGAGCTCC | 8439 |
rs2634488 | snp | C/T | 0.499999 | 0.000798721 | intron-variant | NSMAF | GRCh38.p7 | 8:58598751 | ACAGGTGTGAGCCAC[C/T]GCGCCCAGCCCCTGG | 8439 |
rs2634489 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58598498 | tcttttttttttttt[C/T]tttttttgtttgaga | 8439 |
rs2634527 | snp | A/G | 0.483995 | 0.0880135 | intron-variant | NSMAF | GRCh38.p7 | 8:58586830 | CTTTAGCAATACTTC[A/G]TTTCTTCTTGTATTC | 8439 |
rs2634529 | snp | A/G | 0.188946 | 0.24243 | intron-variant | NSMAF | GRCh38.p7 | 8:58602953 | TAATGATAACCCTGG[A/G]TTAAAATCATGCCCA | 8439 |
rs2634530 | snp | A/C | 0.495135 | 0.0490805 | intron-variant | NSMAF | GRCh38.p7 | 8:58603597 | AAATTATTAAATACA[A/C]TGAGCTATTACACTA | 8439 |
rs2634531 | snp | C/T | 0.497586 | 0.0346604 | intron-variant | NSMAF | GRCh38.p7 | 8:58604499 | AGCTTAATGTATGAA[C/T]AAAATACTAGCTATA | 8439 |
rs2634532 | snp | A/G | 0.121717 | 0.214577 | intron-variant | NSMAF | GRCh38.p7 | 8:58606960 | AGCTCTATACCCAAA[A/G]GAGGAGATTTTTAAT | 8439 |
rs2634533 | snp | C/G | 0.118933 | 0.212888 | intron-variant | NSMAF | GRCh38.p7 | 8:58623063 | AGGAGAACTCTCTAG[C/G]GCTTCCTCAACTCTT | 8439 |
rs2634534 | snp | C/T | 0.494484 | 0.0522255 | intron-variant | NSMAF | GRCh38.p7 | 8:58614479 | AGGTTATAGGATAAG[C/T]CTGTGCCTAGGCAAA | 8439 |
rs2680896 | snp | A/G | 0.16618 | 0.23553 | intron-variant | NSMAF | GRCh38.p7 | 8:58603922 | AAGAAGAAAACAGGC[A/G]TTTGGCAGGAGGACC | 8439 |
rs2680897 | snp | A/G | 0.494143 | 0.0537956 | intron-variant | NSMAF | GRCh38.p7 | 8:58607078 | CAAATTAAAAGCACA[A/G]AAATAAGAATTAAAA | 8439 |
rs2680898 | snp | A/G | 0.121717 | 0.214577 | intron-variant | NSMAF | GRCh38.p7 | 8:58607232 | AGTAAGACATGTGTC[A/G]GAAATAGGACCTAAG | 8439 |
rs2680899 | snp | C/T | 0.494774 | 0.0508504 | intron-variant | NSMAF | GRCh38.p7 | 8:58609475 | ATACACAGATGCTGC[C/T]TGTGAAGGGGGTGGG | 8439 |
rs2680900 | snp | A/G | 0.122064 | 0.214785 | intron-variant | NSMAF | GRCh38.p7 | 8:58609976 | AGCCATGACAGACAA[A/G]TAAATAATACCAAAT | 8439 |
rs2680901 | snp | C/T | 0.49533 | 0.0480965 | intron-variant | NSMAF | GRCh38.p7 | 8:58610885 | CTGTGGAAGAGAAAG[C/T]CTTTATCACTCCCTC | 8439 |
rs2680903 | snp | C/T | 0.128684 | 0.218592 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58599775 | ACAGATGGTTGACGA[C/T]GTGGAGCTTCCCCCT | 8439 |
rs2680904 | snp | C/T | 0.162253 | 0.234095 | intron-variant | NSMAF | GRCh38.p7 | 8:58598687 | CTTTTGCCCAAATAA[C/T]ACCAAATTCATCCTG | 8439 |
rs2946577 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58600619 | agagcaagactttgt[C/T]tcaaaaaaaaaaaaa | 8439 |
rs2946578 | snp | C/T | 0.493837 | 0.055168 | intron-variant | NSMAF | GRCh38.p7 | 8:58602515 | GTGAATATTATTATT[C/T]TTCAATATTAGCCTA | 8439 |
rs2969915 | snp | A/T | 0.147991 | 0.228242 | intron-variant | NSMAF | GRCh38.p7 | 8:58602569 | CTAGAAATATGATAA[A/T]GTATTTCTCTGAAAA | 8439 |
rs2969916 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58600615 | tttttttttgagaca[A/G]agtcttgctctgtcg | 8439 |
rs3736236 | snp | C/T | 0.046008 | 0.144524 | intron-variant | NSMAF | GRCh38.p7 | 8:58589976 | CCCTGCTCTGTGATT[C/T]GACGTGCAGAATAGC | 8439 |
rs3739327 | snp | A/G | 0.498034 | 0.0312882 | downstream-variant-500B | NSMAF | GRCh38.p7 | 8:58583493 | AGTTACTTAAATAAA[A/G]TGAAAACAGCTTTCT | 8439 |
rs3816846 | snp | C/T | 0.381891 | 0.212379 | intron-variant | NSMAF | GRCh38.p7 | 8:58586678 | GACTACATATTTGAA[C/T]CAGACTAGAGAAACA | 8439 |
rs3816847 | snp | A/G | 0.186737 | 0.241863 | intron-variant | NSMAF | GRCh38.p7 | 8:58603551 | AGTATTTGTTCAGCT[A/G]TGTATAAACAGTTCC | 8439 |
rs3837194 | in-del | -/T | 0.498392 | 0.028309 | downstream-variant-500B | SDCBP, NSMAF | GRCh38.p7 | 8:58583149 | AATATTTAATAACAC[-/T]TGAAACTGACTTTGG | 8439 |
rs4266636 | snp | A/G | 0.419936 | 0.183362 | intron-variant | NSMAF | GRCh38.p7 | 8:58619986 | AAGGTATAATAATTA[A/G]CTTAGTGGTACCAGA | 8439 |
rs4421339 | snp | A/G | 0.0901694 | 0.192235 | intron-variant | NSMAF | GRCh38.p7 | 8:58630098 | CAATCATGTGGTGCT[A/G]TGTGGGACAGAGGAT | 8439 |
rs4598239 | snp | G/T | 0.411746 | 0.190626 | intron-variant | NSMAF | GRCh38.p7 | 8:58620148 | AAACCATTAGAACAG[G/T]AGAAGTGTACTCTCT | 8439 |
rs4737504 | snp | A/G | 0.493969 | 0.05458 | intron-variant | NSMAF | GRCh38.p7 | 8:58628020 | ccaaaatagcatggg[A/G]ctagtataacaacag | 8439 |
rs4737505 | snp | A/G | 0.214843 | 0.247516 | intron-variant | NSMAF | GRCh38.p7 | 8:58644964 | CGGGGACCTGTTGGC[A/G]GGGTGGGGAGCTAGA | 8439 |
rs4738695 | snp | C/G | 0.183886 | 0.241099 | intron-variant | NSMAF | GRCh38.p7 | 8:58609412 | AACAGATCAGAAGAA[C/G]TCAAACTTCAGAGAC | 8439 |
rs4738696 | snp | C/T | 0.305436 | 0.243776 | intron-variant | NSMAF | GRCh38.p7 | 8:58611577 | GTTTCAGCAGAGAAA[C/T]AGAAACTATGAAAAA | 8439 |
rs4738697 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | NSMAF | GRCh38.p7 | 8:58620467 | CCATGTTAAGGTGTT[C/T]AGGCTTTATCCTGAA | 8439 |
rs4738699 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | NSMAF | GRCh38.p7 | 8:58654830 | ATCTAAATTTCTTTT[C/T]TATTATGTATTTATT | 8439 |
rs5891688 | in-del | -/TGAT | 0.383053 | 0.211653 | downstream-variant-500B | SDCBP, NSMAF | GRCh38.p7 | 8:58583103 | ACTCATTGAGGCTAC[-/TGAT]TGATTGTCCCTAGCA | 8439 |
rs5891689 | in-del | -/ATTG | | | downstream-variant-500B | SDCBP, NSMAF | GRCh38.p7 | 8:58583109 | TGAGGCTACTGATTG[-/ATTG]TCCCTAGCAATACCT | 8439 |
rs5891691 | in-del | -/A | 0.365024 | 0.221967 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660100 | GTGTCCTCCATTGTG[-/A]AAAAAAAAAAAAGAC | 8439 |
rs6471732 | snp | C/T | 0.419296 | 0.183954 | intron-variant | NSMAF | GRCh38.p7 | 8:58626583 | attccatggtgtata[C/T]atataggactttttc | 8439 |
rs6985007 | snp | G/T | 0.499954 | 0.00479211 | intron-variant | NSMAF | GRCh38.p7 | 8:58649186 | tcataggagattatt[G/T]tggagttttaagatt | 8439 |
rs6985643 | snp | A/G | 0.499839 | 0.00898417 | intron-variant | NSMAF | GRCh38.p7 | 8:58649528 | atgtttgtcccctcc[A/G]aatctcatgttaata | 8439 |
rs6991020 | snp | A/G | 0.497959 | 0.0318836 | intron-variant | NSMAF | GRCh38.p7 | 8:58592819 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 8439 |
rs6991479 | snp | C/T | 0.305186 | 0.243833 | intron-variant | NSMAF | GRCh38.p7 | 8:58610191 | AATACATTTGAGTAA[C/T]TGTATATTCCTTTGT | 8439 |
rs6991644 | snp | A/G | 0.307671 | 0.243257 | intron-variant | NSMAF | GRCh38.p7 | 8:58610347 | GAAAAAATAAGGGAA[A/G]ACAACCAAATCATCA | 8439 |
rs6994461 | snp | C/T | 0.17332 | 0.23795 | intron-variant | NSMAF | GRCh38.p7 | 8:58654609 | AATATTATACACTCA[C/T]GGAATGTCTGAAACA | 8439 |
rs6994565 | snp | C/T | 0.130351 | 0.219509 | intron-variant | NSMAF | GRCh38.p7 | 8:58598854 | atggtgaaaccgtca[C/T]gaccaaaaaaaatac | 8439 |
rs6994622 | snp | C/G/T | 0.0209503 | 0.100241 | intron-variant | NSMAF | GRCh38.p7 | 8:58656488 | ataaaaatatcatat[C/G/T]cccagttacatttga | 8439 |
rs6995115 | snp | A/G | 0.498369 | 0.0285077 | intron-variant | NSMAF | GRCh38.p7 | 8:58586055 | CAGAATGTGGTTTAC[A/G]TTATTCTGGATTTTA | 8439 |
rs6998210 | snp | C/T | 0.418007 | 0.185132 | intron-variant | NSMAF | GRCh38.p7 | 8:58625691 | ccgaaaatgagtctc[C/T]tgcagatggcatata | 8439 |
rs7001188 | snp | C/T | 0.111224 | 0.207945 | intron-variant | NSMAF | GRCh38.p7 | 8:58645004 | gcattaggagaaata[C/T]ctaatgtagatgatg | 8439 |
rs7006797 | snp | A/G | 0.496999 | 0.0386216 | intron-variant | NSMAF | GRCh38.p7 | 8:58588588 | AAGCAAATAGGCATC[A/G]AAGATGCTCGCTTCA | 8439 |
rs7006937 | snp | C/G | 0.414905 | 0.187899 | intron-variant | NSMAF | GRCh38.p7 | 8:58618624 | taacacacacacaca[C/G]aGAGCAACAATGTGA | 8439 |
rs7008292 | snp | C/T | 0.130351 | 0.219509 | intron-variant | NSMAF | GRCh38.p7 | 8:58597156 | GCCAACTTTCACTCA[C/T]ATTCAATTGCCAGAA | 8439 |
rs7011033 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | NSMAF | GRCh38.p7 | 8:58618909 | TTTCATTTCATATGG[C/T]AAAAATCCCTTCCCC | 8439 |
rs7011066 | snp | C/G | 0.412082 | 0.190341 | intron-variant | NSMAF | GRCh38.p7 | 8:58618972 | ATACATTAAAACGTT[C/G]ACAGTGAACTATTTT | 8439 |
rs7014666 | snp | C/G | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58632073 | CCTGTACTTTCCTCA[C/G]TGCTTTTCCTCCTGC | 8439 |
rs7015319 | snp | A/G | 0.26326 | 0.249648 | intron-variant | NSMAF | GRCh38.p7 | 8:58594912 | CATGACCTGTATGCC[A/G]GAGGGGCTGTCTGTC | 8439 |
rs7015870 | snp | G/T | 0.0952156 | 0.196321 | intron-variant | NSMAF | GRCh38.p7 | 8:58625386 | tatgtctgtatatat[G/T]tatatgcatatgtat | 8439 |
rs7465261 | snp | C/T | | | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660356 | ggagggtgggggatt[C/T]ttgctaaactgccgt | 8439 |
rs7816499 | snp | C/T | 0.305436 | 0.243776 | intron-variant | NSMAF | GRCh38.p7 | 8:58612566 | ctaaggaatgtgttg[C/T]gggaatctctgattt | 8439 |
rs7820921 | snp | A/C | 0.493386 | 0.0571263 | intron-variant | NSMAF | GRCh38.p7 | 8:58650097 | AAGCACTTGGGTACC[A/C]TTTGCATCTTCACCC | 8439 |
rs7825739 | snp | C/T | 0.418814 | 0.184396 | intron-variant | NSMAF | GRCh38.p7 | 8:58606917 | AAAGCACTTAATCAA[C/T]GTTAATTTCTTCTCT | 8439 |
rs7826122 | snp | A/G | 0.499502 | 0.0157669 | intron-variant | NSMAF | GRCh38.p7 | 8:58593570 | CCCTTCCATCTCTGC[A/G]TCTTCCAGAGTGCCA | 8439 |
rs7826603 | snp | A/G | 0.499527 | 0.0153681 | intron-variant | NSMAF | GRCh38.p7 | 8:58593628 | AAGACATACTTTAAT[A/G]AATAATATATAATGC | 8439 |
rs7830228 | snp | A/C | 0.498611 | 0.0263212 | intron-variant | NSMAF | GRCh38.p7 | 8:58657617 | GATTCCAGTGCATAC[A/C]TGATGTGAGACAGAT | 8439 |
rs7831185 | snp | A/G | 0.121717 | 0.214577 | intron-variant | NSMAF | GRCh38.p7 | 8:58617494 | acccatcaaaaagtg[A/G]gcaaaggatatgaac | 8439 |
rs7833097 | snp | A/G | 0.110519 | 0.207473 | intron-variant | NSMAF | GRCh38.p7 | 8:58635709 | ATTAACTGGTAAAAC[A/G]AAACACAGAATAGTG | 8439 |
rs7833791 | snp | C/T | 0.409382 | 0.192607 | intron-variant | NSMAF | GRCh38.p7 | 8:58630142 | cacaaatttttatac[C/T]ggctttgatgtggtt | 8439 |
rs7836960 | snp | C/T | 0.493793 | 0.055364 | intron-variant | NSMAF | GRCh38.p7 | 8:58634011 | ATGAAAACCCTATCT[C/T]CAAGTCAAAAAGTAC | 8439 |
rs7840932 | snp | A/G | 0.498369 | 0.0285077 | intron-variant | NSMAF | GRCh38.p7 | 8:58589256 | AGATATATTTTATAT[A/G]TATTTTTTAAACACA | 8439 |
rs7841618 | snp | C/T | 0.305685 | 0.24372 | intron-variant | NSMAF | GRCh38.p7 | 8:58610835 | TAAAGCACAAAGATA[C/T]CTCTAGAATCCTTCA | 8439 |
rs7844231 | snp | G/T | 0.49949 | 0.0159663 | intron-variant | NSMAF | GRCh38.p7 | 8:58593473 | ATGATAAAGACTAAA[G/T]AACGAGTAGCCTTAC | 8439 |
rs10086028 | snp | G/T | 0.370974 | 0.218781 | intron-variant | NSMAF | GRCh38.p7 | 8:58612325 | actatgaggctggga[G/T]agcttctgggttgct | 8439 |
rs10086130 | snp | A/G | 0.192088 | 0.2432 | intron-variant | NSMAF | GRCh38.p7 | 8:58605399 | CTCATAAACTAATAT[A/G]AGACCTGACTGAACA | 8439 |
rs10086457 | snp | C/G | 0.293294 | 0.246223 | intron-variant | NSMAF | GRCh38.p7 | 8:58605629 | AAAGAGGCGATTCTA[C/G]AAATAGCATTTTTCT | 8439 |
rs10087843 | snp | C/T | 0.413748 | 0.188909 | intron-variant | NSMAF | GRCh38.p7 | 8:58621783 | gcatgtatgtctttt[C/T]ttgaaaagtgtctgt | 8439 |
rs10088312 | snp | A/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58639015 | aatgggtgggtgtgg[A/T]ggctcacgcctgtaa | 8439 |
rs10088541 | snp | A/G | 0.411914 | 0.190483 | intron-variant | NSMAF | GRCh38.p7 | 8:58618348 | TAATATGAAGCTATA[A/G]GATGatattatgatt | 8439 |
rs10090212 | snp | A/G | 0.43309 | 0.17023 | intron-variant | NSMAF | GRCh38.p7 | 8:58643597 | GAGTAAAATGGCGCA[A/G]TCTCAGCTCAAGTAA | 8439 |
rs10090837 | snp | G/T | 0.417683 | 0.185425 | intron-variant | NSMAF | GRCh38.p7 | 8:58621978 | ctttagtttaattag[G/T]tctcatttgtcaatt | 8439 |
rs10091952 | snp | A/G | 0.37138 | 0.218556 | intron-variant | NSMAF | GRCh38.p7 | 8:58631854 | GCAGACAGGGAAGGA[A/G]GCTAATCCAAGTGCT | 8439 |
rs10093782 | snp | A/G | 0.191147 | 0.242974 | intron-variant | NSMAF | GRCh38.p7 | 8:58607161 | AAAAAATGAATTTCT[A/G]TTGGTGTCGAATTAA | 8439 |
rs10098355 | snp | A/G | 0.19334 | 0.243495 | intron-variant | NSMAF | GRCh38.p7 | 8:58638508 | atcatccacaaaggt[A/G]ccaaaaacacacaat | 8439 |
rs10099231 | snp | C/T | 0.19334 | 0.243495 | intron-variant | NSMAF | GRCh38.p7 | 8:58626256 | ggcacttgcctcgcc[C/T]ggctaattttttgta | 8439 |
rs10103176 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58654904 | caatggcacaatctc[A/G]gctcactgcaacctc | 8439 |
rs10103279 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58654897 | tggagtgcaatggca[C/T]aatctcagctcactg | 8439 |
rs10107530 | snp | A/T | 0.380138 | 0.213458 | intron-variant | NSMAF | GRCh38.p7 | 8:58589208 | TAACAGATATTATAT[A/T]TTAAATATAAATAAT | 8439 |
rs10111180 | snp | C/T | 0.43132 | 0.172114 | intron-variant | NSMAF | GRCh38.p7 | 8:58599197 | TGCTAAATATTCACC[C/T]AATGCTAAATAAAAT | 8439 |
rs10112330 | snp | C/T | 0.414245 | 0.188477 | intron-variant | NSMAF | GRCh38.p7 | 8:58638012 | agaaattaacattga[C/T]attgacccacaaaat | 8439 |
rs10113323 | snp | A/G | 0.394354 | 0.204112 | intron-variant | NSMAF | GRCh38.p7 | 8:58642147 | TTTACTTTAGCTTGT[A/G]TTTAAACAAATACCA | 8439 |
rs10113667 | snp | A/T | 0.369346 | 0.219673 | intron-variant | NSMAF | GRCh38.p7 | 8:58612326 | ctatgaggctgggag[A/T]gcttctgggttgctg | 8439 |
rs10113830 | snp | A/C | 0.398903 | 0.200818 | intron-variant | NSMAF | GRCh38.p7 | 8:58635245 | AATACAGATAAAAGT[A/C]ATTAAATATATACAG | 8439 |
rs10504257 | snp | A/C | 0.0901694 | 0.192235 | intron-variant | NSMAF | GRCh38.p7 | 8:58631628 | AATCAGAACATTATC[A/C]ATCAAAAGTTTTAAA | 8439 |
rs10656601 | in-del | -/AT/ATAT | 0.574554 | 0.104622 | intron-variant | NSMAF | GRCh38.p7 | 8:58604557 | ACATAGATATATATA[-/AT/ATAT]ATATATATATATAAA | 8439 |
rs10710122 | in-del | -/A | 0.135143 | 0.222054 | intron-variant | NSMAF | GRCh38.p7 | 8:58592566 | GAGAAAAACAAACAG[-/A]AAAAAACAAAAGCTT | 8439 |
rs10957061 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | NSMAF | GRCh38.p7 | 8:58611232 | ACTTTAAGATAACTA[C/T]AGTAAATATGATAAA | 8439 |
rs10957062 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58611491 | TCAGCCATGATTATG[A/C]CACTGCACTCCAGCC | 8439 |
rs10957063 | snp | A/G | 0.412583 | 0.189912 | intron-variant | NSMAF | GRCh38.p7 | 8:58630741 | TCAGCACATGCAAGT[A/G]TTTCTTGTCCGTAAA | 8439 |
rs11337086 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58645114 | ACTTAAAGTATAATT[-/A]AAAAAAAAAAAAAAA | 8439 |
rs11431046 | in-del | -/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58624036 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGT | 8439 |
rs11774558 | snp | A/T | 0.379746 | 0.213696 | intron-variant | NSMAF | GRCh38.p7 | 8:58588367 | GTACAGTTTCCATTT[A/T]ATTTTTCTCCAGAGA | 8439 |
rs11774998 | snp | C/G | 0.412917 | 0.189626 | intron-variant | NSMAF | GRCh38.p7 | 8:58636784 | ctgtagtttgccaag[C/G]cctgctgtgaatcca | 8439 |
rs11777487 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58635128 | CTACAAGTAATTTCA[C/T]TCATGCACATATATA | 8439 |
rs11780640 | snp | G/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58603001 | CTTCAAGAAGTATGG[G/T]GGAAAAAACATACAT | 8439 |
rs11782455 | snp | A/G | 0.379354 | 0.213933 | intron-variant | NSMAF | GRCh38.p7 | 8:58589304 | TCCTTACACTCACAC[A/G]CTTTGTGAAAAAGAG | 8439 |
rs11784708 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | NSMAF | GRCh38.p7 | 8:58609426 | ACTCAAACTTCAGAG[A/C]CTACACATCACGATT | 8439 |
rs11785141 | snp | C/T | 0.426528 | 0.177025 | intron-variant | NSMAF | GRCh38.p7 | 8:58588466 | CCCGCAGGTCTAAAT[C/T]GGGGTGGGGGTGTTC | 8439 |
rs11985566 | snp | C/T | 0.416708 | 0.186302 | intron-variant | NSMAF | GRCh38.p7 | 8:58627555 | tcagtagcactgcta[C/T]acaccaacaacggcc | 8439 |
rs11994921 | snp | C/T | 0.411914 | 0.190483 | intron-variant | NSMAF | GRCh38.p7 | 8:58616988 | AAATATCTAGGAATA[C/T]GTCCAACAAAAGATG | 8439 |
rs11994937 | snp | C/T | 0.0792508 | 0.182605 | intron-variant | NSMAF | GRCh38.p7 | 8:58596021 | TGCAACAATTTTGTT[C/T]TGGTGTGGGGTGGGG | 8439 |
rs11995355 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | NSMAF | GRCh38.p7 | 8:58591248 | GCAGAAAGTTACAGG[A/G]AGGAAAATAGCAATT | 8439 |
rs12056696 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NSMAF | GRCh38.p7 | 8:58601154 | AAAAAGCCTGAGAGG[A/T]ATAGATAGAACAATT | 8439 |
rs12171634 | snp | G/T | 0.41141 | 0.19091 | intron-variant | NSMAF | GRCh38.p7 | 8:58626092 | tccattatataattc[G/T]ttttttttttttttt | 8439 |
rs12171670 | snp | C/T | 0.419296 | 0.183954 | intron-variant | NSMAF | GRCh38.p7 | 8:58626161 | tggagtgcagtggcg[C/T]gatcttggctctctg | 8439 |
rs12334684 | snp | A/G | 0.493013 | 0.058691 | intron-variant | NSMAF | GRCh38.p7 | 8:58628827 | ttggcaggcattttt[A/G]tttgtttgttttatt | 8439 |
rs12674724 | snp | A/G | 0.461259 | 0.133677 | intron-variant | NSMAF | GRCh38.p7 | 8:58600396 | TTGGGAGGCCAAGGC[A/G]GGTGGATCACGAAGT | 8439 |
rs12677290 | snp | A/G | 0.469295 | 0.120041 | intron-variant | NSMAF | GRCh38.p7 | 8:58585631 | AGAACAAAGATCAAG[A/G]CAACTGCAGTAGCTG | 8439 |
rs12679938 | snp | G/T | 0.34437 | 0.231505 | intron-variant | NSMAF | GRCh38.p7 | 8:58586126 | CAAAATCCTTGTACT[G/T]AAGCAATGACTATCC | 8439 |
rs12682397 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58624062 | tttttttttttttga[A/G]acagagtcttgttct | 8439 |
rs12682645 | snp | G/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58635026 | TGAAGAAGCTCATTA[G/T]GGATCACATCTTTTT | 8439 |
rs13248968 | snp | C/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58642822 | CTCCAAAAGACTCTC[C/T]TAGGTTATAATCCTC | 8439 |
rs13251087 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58642846 | AATCCTCAATAAAAG[G/T]Ctaaataaaatttac | 8439 |
rs13253245 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | NSMAF | GRCh38.p7 | 8:58630363 | GTATTATAATTCACA[C/T]TGGAACAAAAGAGCT | 8439 |
rs13263085 | snp | A/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58640537 | AATAGTATACTAATA[A/C]CAACAATATTGCAAC | 8439 |
rs13263086 | snp | A/C | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58640540 | AGTATACTAATAACA[A/C]CAATATTGCAACTGG | 8439 |
rs13263515 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58640425 | TTTTCTTTTATACTG[A/G]AAAATCTGAGTCTTG | 8439 |
rs13265063 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58640400 | TTCTTTAATATTACA[G/T]GTATGTCTCTTTTCT | 8439 |
rs13265070 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58640406 | AATATTACATGTATG[G/T]CTCTTTTCTTTTATA | 8439 |
rs13265082 | snp | A/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58640418 | ATGTCTCTTTTCTTT[A/T]ATACTGGAAAATCTG | 8439 |
rs13270855 | snp | C/T | 0.12932 | 0.218944 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58659942 | GGCCAGCGGCCAGAC[C/T]AGGATCCGACCTCAC | 8439 |
rs13438863 | snp | C/T | 0.0520825 | 0.152737 | intron-variant | NSMAF | GRCh38.p7 | 8:58635973 | TCAGTGCTCAATATA[C/T]ATGTACTGAATAGAT | 8439 |
rs13439297 | snp | A/T | 0.0460142 | 0.144533 | intron-variant | NSMAF | GRCh38.p7 | 8:58599685 | CTAAGCAATAAAATA[A/T]TTACTGAAATTGCAC | 8439 |
rs16923584 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NSMAF | GRCh38.p7 | 8:58588824 | TAACTATAATCAACT[A/G]ATATTTCTGATCATG | 8439 |
rs16923588 | snp | A/G | 0.472285 | 0.114409 | intron-variant | NSMAF | GRCh38.p7 | 8:58595517 | AAGACCCTAACTTTT[A/G]CCAGGACTATCAGCT | 8439 |
rs16923594 | snp | C/T | 0.44546 | 0.155869 | intron-variant | NSMAF | GRCh38.p7 | 8:58598309 | GGAAGAAGATAAGCA[C/T]TGAAACTGAAGAGAA | 8439 |
rs16923600 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | NSMAF | GRCh38.p7 | 8:58601626 | AAAAGAAATCATAAC[A/C]TAGATATACCATATT | 8439 |
rs16923629 | snp | A/C | 0.254664 | 0.249956 | intron-variant | NSMAF | GRCh38.p7 | 8:58651441 | GCTGGACTCTAGAAA[A/C]TTACATTCTCCCTGA | 8439 |
rs16923631 | snp | A/G | 0.193653 | 0.243567 | intron-variant | NSMAF | GRCh38.p7 | 8:58652514 | AGCCACACATGCTGA[A/G]CTGGGATGAGTGAGC | 8439 |
rs16923635 | snp | A/C/G | 0.145978 | 0.227331 | intron-variant | NSMAF | GRCh38.p7 | 8:58653093 | AGGATGGGGGCACAG[A/C/G]AGTTAAGTGTTCCAA | 8439 |
rs16923636 | snp | A/G | 0.101301 | 0.200969 | intron-variant | NSMAF | GRCh38.p7 | 8:58653186 | ATGCTTATGTTTTAA[A/G]GATAAGCATTAGAAA | 8439 |
rs16923637 | snp | G/T | 0.332106 | 0.236133 | intron-variant | NSMAF | GRCh38.p7 | 8:58655326 | ATCCCAACACTCCAC[G/T]GTGGATAGTAAAGCA | 8439 |
rs17206144 | snp | C/T | 0.031825 | 0.122064 | intron-variant | NSMAF | GRCh38.p7 | 8:58603470 | TAACGTGTAGACCAT[C/T]CCTGTGCATTCTTGA | 8439 |
rs17206746 | snp | A/T | 0.372189 | 0.218105 | intron-variant | NSMAF | GRCh38.p7 | 8:58631693 | TGCTTTAGTATTAGT[A/T]CTAGTATGGCTTTAA | 8439 |
rs17265530 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | NSMAF | GRCh38.p7 | 8:58602214 | AATTCAAATATACAC[A/G]TTTACTTCCACAAAA | 8439 |
rs17272151 | snp | A/G | 0.370365 | 0.219117 | intron-variant | NSMAF | GRCh38.p7 | 8:58608152 | CAGGTTAGATTGTGG[A/G]GTGATAAGAAATATA | 8439 |
rs17272647 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NSMAF | GRCh38.p7 | 8:58631870 | GCTAATCCAAGTGCT[A/G]ATTTTTTAAGAAACG | 8439 |
rs17273109 | snp | C/T | 0.15665 | 0.231917 | intron-variant | NSMAF | GRCh38.p7 | 8:58655616 | GCCATCCCTGACAAA[C/T]CCAAGGAAGACATGT | 8439 |
rs28373260 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58585332 | GTTTTTTTTTTTTCT[C/T]TTTTTTTACTATTCT | 8439 |
rs28429099 | snp | A/T | 0.410568 | 0.191619 | intron-variant | NSMAF | GRCh38.p7 | 8:58632503 | GAAGCAGTTTTCCAC[A/T]TGGCTTCCTGGACAC | 8439 |
rs28489122 | snp | A/G | 0.436408 | 0.16659 | intron-variant | NSMAF | GRCh38.p7 | 8:58632795 | CCCCTTGGAGTTCTC[A/G]TGGCCATCTTAAATC | 8439 |
rs28507102 | snp | A/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58598489 | AAGACTCTGTCTCAA[A/C]CAAAAAAAAAAAAAA | 8439 |
rs28548238 | snp | A/G | 0.192715 | 0.243348 | intron-variant | NSMAF | GRCh38.p7 | 8:58645910 | GCCAGGCGTGGTGGC[A/G]GGCGCCTATAATCCC | 8439 |
rs28623575 | snp | A/C | 0.405082 | 0.196086 | intron-variant | NSMAF | GRCh38.p7 | 8:58592917 | CAAAAACAACAACAA[A/C]AAAAAAAAAACCTCT | 8439 |
rs28655100 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58585330 | GGGTTTTTTTTTTTT[C/T]TCTTTTTTTACTATT | 8439 |
rs28655813 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58654954 | ATTCTCTTGTCTCAG[C/T]CTCCCGAGTAGCTGG | 8439 |
rs28674507 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58654969 | TCTCCCGAGTAGCTG[A/G]GATTACAGGTGTGTG | 8439 |
rs28686801 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58654960 | TTGTCTCAGTCTCCC[A/G]AGTAGCTGGGATTAC | 8439 |
rs28688734 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | NSMAF | GRCh38.p7 | 8:58598567 | TTCCATAGGAATTGA[A/G]GCCACTGTTCTATCA | 8439 |
rs28697918 | snp | A/T | 0.0228947 | 0.104514 | intron-variant | NSMAF | GRCh38.p7 | 8:58591471 | ATTTTCTTGTGTAAC[A/T]GAAACCTTCCTTTTT | 8439 |
rs28710949 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58654911 | ACAATCTCAGCTCAC[C/T]GCAACCTCTGCCTCC | 8439 |
rs28755983 | snp | C/T | 0.409891 | 0.192184 | intron-variant | NSMAF | GRCh38.p7 | 8:58633019 | TGGATTCCTGGAACA[C/T]CCCAATAGGTCTCCT | 8439 |
rs28819228 | snp | G/T | 0.485324 | 0.0843964 | intron-variant | NSMAF | GRCh38.p7 | 8:58639722 | TGTCCATTGATAGAT[G/T]AATGAATAAAGAAAA | 8439 |
rs28886919 | snp | A/G | 0.415235 | 0.18761 | intron-variant | NSMAF | GRCh38.p7 | 8:58621501 | GCTGGGTCAAATGGT[A/G]GCTCTGTTTTAAGTT | 8439 |
rs33942423 | in-del | -/A/AA/AAA/AAAA/AAAAA | 0.737074 | 0.120428 | intron-variant | NSMAF | GRCh38.p7 | 8:58601546 | GTGTCTAGAATACAG[-/A/AA/AAA/AAAA/AAAAA]AAAAAAAAAAAAAAA | 8439 |
rs34054274 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58624035 | GGTATAGAGTTAGGA[-/T]TTTTTTTTTTTTTTT | 8439 |
rs34092757 | snp | A/C | 0 | 0 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661287 | TGAACCACCCCTCCC[A/C]TATGGTATATAAGCC | 8439 |
rs34191934 | in-del | -/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58659180 | AAGGGGGTGCCCGCC[-/G]GGCAGCGTACTCACC | 8439 |
rs34591986 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58652405 | CCTGACCATGCCAGG[-/A]AAAAGGCTGGTGTTT | 8439 |
rs34637164 | snp | C/T | 0.0289792 | 0.116832 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58597388 | TTTACAAAATTTACC[C/T]GGGGAATCTGCCATA | 8439 |
rs34638032 | in-del | -/ACAC | 0.492679 | 0.0600586 | intron-variant | NSMAF | GRCh38.p7 | 8:58637018 | ACTGATTAAGATTAT[-/ACAC]ACACACACACACACA | 8439 |
rs34689462 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58651216 | AAAAGACCTGGCTCA[-/T]TTTTATTATCCATGT | 8439 |
rs34780319 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58609248 | ATATTTCAAAATCTA[-/T]TTTCTTATTAATCAT | 8439 |
rs34989196 | in-del | -/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58655261 | ACAAGTGTAAGCCAT[-/G]GCACCTAGGCAAGTA | 8439 |
rs35037523 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58644144 | GGGACTTGAGATGGG[-/C]CCTTAAGTTCCAGTG | 8439 |
rs35129339 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58623443 | AGTATCATAAACAGA[-/C]CATGAATTTATTTTT | 8439 |
rs35188110 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58643431 | CTGACTGAACAATGC[-/T]TAGGCTTCCCCACCT | 8439 |
rs35189286 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58631208 | AAATTCTCAGTAACA[-/C]CCCAGTAAATAATCT | 8439 |
rs35190779 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58592685 | TGAGGTCAGGAGTTC[-/A]AAGACCAACCTGGCC | 8439 |
rs35209612 | in-del | -/AAAA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58600646 | AAAAAAAAAAAAAAA[-/AAAA]GATTAGCACCACTAT | 8439 |
rs35234411 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58595991 | GTTTCAAAAACCTGA[-/C]CAGTTGCCTAAGAAT | 8439 |
rs35286551 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58594609 | CGTTTGACCATCACC[-/A]AAAGGACAAACTCTT | 8439 |
rs35319550 | in-del | -/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58645770 | AATAGGCCAGGCGCA[-/G]CGGCTCACACCTGTA | 8439 |
rs35328777 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58624059 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTTGT | 8439 |
rs35369541 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58591731 | GCTTCAAGTGATCCG[-/C]CCCCTTCGGCCTCCC | 8439 |
rs35393291 | in-del | -/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58658289 | TGAGTTACATAGTTA[-/G]GGGCTCAGTTATTTA | 8439 |
rs35395804 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58600576 | CAGTGAGCTGAGATT[C/T]TGCTCACTGTACTCC | 8439 |
rs35436008 | snp | A/G/T | 1.65512e-05 | 0.00287669 | stop-gained, missense | NSMAF | GRCh38.p7 | 8:58635511 | GGTTCAAAAATCACC[A/G/T]ATTTTGAACATATTT | 8439 |
rs35465191 | in-del | -/CT | | | intron-variant | NSMAF | GRCh38.p7 | 8:58598850 | AACATGGTGAAACCG[-/CT]TCACGACCAAAAAAA | 8439 |
rs35492874 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58590153 | CTATCTTATACATTT[-/C]CCGAAAAATTAATGC | 8439 |
rs35634753 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58586320 | ATAAAGCAGTGTTAG[-/C]CATTGGCAAAACCTC | 8439 |
rs35663505 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58644153 | GATGGGCCTTAAGTT[-/C]CCAGTGTGTTGGAGG | 8439 |
rs35666144 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58614705 | GTCATTTGGACGCTG[-/A]AGTCAGCTGGGCCTG | 8439 |
rs35668952 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58657258 | AGAAATAAATGCTCA[-/T]TTTCAAGTTTCTTTT | 8439 |
rs35747457 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58593034 | TGGTTAACAAGGTCA[-/T]TACAAGTACAACTGT | 8439 |
rs35776754 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58584456 | GAATTATGGATATAG[-/A]AACAATGCAAATAAA | 8439 |
rs35906151 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58619916 | TTGAAGACATAAGTG[-/A]AAAAGGAAAATAAGG | 8439 |
rs36011709 | in-del | -/CC | | | intron-variant | NSMAF | GRCh38.p7 | 8:58654816 | ACATATCTCAACTAT[-/CC]CTAAATTTCTTTTCT | 8439 |
rs36053026 | in-del | -/TAA | 0.495708 | 0.0461266 | intron-variant | NSMAF | GRCh38.p7 | 8:58600770 | TCTCAGTGTGGTGGG[-/TAA]ATACCAAGTAAACTT | 8439 |
rs36064879 | in-del | -/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58632942 | GTCAGCACATCTGTT[-/G]GGGTTTTCTTCAGAA | 8439 |
rs36067275 | snp | C/T | 0.00276268 | 0.0370635 | missense | NSMAF | GRCh38.p7 | 8:58599358 | TCTGGAGAAAGTCCT[C/T]GGGACCTATTAGATT | 8439 |
rs36136766 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58604550 | ATATAACTACATAGA[-/T]ATATATAATATATAT | 8439 |
rs55658192 | snp | G/T | 0.305436 | 0.243776 | intron-variant | NSMAF | GRCh38.p7 | 8:58613520 | AGTACTGAAAAATAC[G/T]AGAATTACCGAAAAG | 8439 |
rs55719287 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58605099 | TAGCAACTTTGTAAA[C/T]TAGAATAATTTAATT | 8439 |
rs55909077 | snp | A/G | 0.164873 | 0.23506 | intron-variant | NSMAF | GRCh38.p7 | 8:58602520 | TATTATTATTCTTCA[A/G]TATTAGCCTATTTGA | 8439 |
rs55965030 | in-del | -/T | 0.402845 | 0.197835 | intron-variant | NSMAF | GRCh38.p7 | 8:58595686 | ACATTAAATTTTTGC[-/T]AAGTCAACTAAGTTA | 8439 |
rs56249776 | snp | C/T | 0.379942 | 0.213577 | intron-variant | NSMAF | GRCh38.p7 | 8:58590366 | GGAGTAAATCTCCAG[C/T]TGGGGGCAGACTGGG | 8439 |
rs56337961 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | NSMAF | GRCh38.p7 | 8:58618570 | AAAAATATATACACA[C/T]ATATATATAATACAA | 8439 |
rs56900658 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58635141 | CATTCATGCACATAT[-/A]TAAGAATGTTCATTC | 8439 |
rs57177969 | in-del | -/AA/AAA/AAAA/AAAAG/AAAG/AAAT/AAG/AG/G | 0.00173957 | 0.0294512 | intron-variant | NSMAF | GRCh38.p7 | 8:58601560 | GAAAAAAAAAAAAAA[lengthTooLong]TAGAGCTAAGTGTTG | 8439 |
rs57204135 | in-del | -/AGA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58639320 | AGAAGAAGAAGAAGA[-/AGA]CATACAAATGGCCAA | 8439 |
rs57382087 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58607519 | GAATGAGAAACTCAA[A/G]GGCACTCTAGCCCTC | 8439 |
rs57658577 | snp | C/T | 0.021333 | 0.101051 | intron-variant | NSMAF | GRCh38.p7 | 8:58616224 | AACAACAATCCTACA[C/T]AAACTTTTTCTGAAA | 8439 |
rs57773582 | snp | C/G | 0.111224 | 0.207945 | intron-variant | NSMAF | GRCh38.p7 | 8:58647440 | CCCAGTAATACACTG[C/G]ACAGTGATATAGTTT | 8439 |
rs57883071 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58655096 | CACCCACCTTGGCCT[C/G]CCAAAGTTCTGGGAC | 8439 |
rs58238055 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58654898 | GGAGTGCAATGGCAC[A/G]ATCTCAGCTCACTGC | 8439 |
rs58306865 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58593690 | AGTAAGGGATGCTTT[C/T]TGCTTTACAGCTATA | 8439 |
rs58563498 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58641741 | ATAACTGCCAGTTCT[C/T]TTTGAAATGGTATCC | 8439 |
rs58627447 | snp | C/T | 0.079696 | 0.183021 | intron-variant | NSMAF | GRCh38.p7 | 8:58643097 | GGGGCGAAAAAACAA[C/T]TTTCAGTTTATTTTT | 8439 |
rs58863335 | snp | A/G | 0.180383 | 0.240111 | intron-variant | NSMAF | GRCh38.p7 | 8:58657915 | GAATTCTAACAAAGC[A/G]GCATATACATGGAAA | 8439 |
rs58866790 | snp | A/C | 0.19334 | 0.243495 | intron-variant | NSMAF | GRCh38.p7 | 8:58642571 | CCGAATAATTGAGAG[A/C]AGAGGATACTGCATA | 8439 |
rs59030019 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58586102 | CCTAATCTCCACATT[A/C/T]GTTTTCTTCAAAATC | 8439 |
rs59063037 | in-del | -/A | | | intron-variant | NSMAF | GRCh38.p7 | 8:58607151 | TCAAAGGAGAAAAAA[-/A]TGAATTTCTATTGGT | 8439 |
rs59104727 | snp | C/T | 0.110519 | 0.207473 | intron-variant | NSMAF | GRCh38.p7 | 8:58638575 | AAAACTAGATATCCC[C/T]GTGGAAAAAAAAAAG | 8439 |
rs59269342 | snp | A/C | 0.0537552 | 0.154881 | intron-variant | NSMAF | GRCh38.p7 | 8:58607751 | ATCATGCCCCAGCAC[A/C]GCCTCCCAAGGACTC | 8439 |
rs59589377 | in-del | -/AAA | | | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660112 | TGAAAAAAAAAAAAA[-/AAA]GACGGAAGTTAAAGG | 8439 |
rs59606339 | snp | A/C | 0.191755 | 0.24312 | missense, intron-variant | NSMAF | GRCh38.p7 | 8:58659297 | GACCTGCACTGCCGG[A/C]TAGCTCGGCATGCCT | 8439 |
rs59644857 | snp | C/T | 0.227074 | 0.248947 | intron-variant | NSMAF | GRCh38.p7 | 8:58584375 | AATTAAAAATAATTG[C/T]TTGGTACAAAGATCT | 8439 |
rs60099840 | in-del | -/T/TATA | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58604570 | TAATATATATATATA[-/T/TATA]AACCTACTTTAAAAT | 8439 |
rs60214509 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58588335 | TAACTTGACATTTTC[-/T]TTTTTTTTTTTTTTA | 8439 |
rs60289621 | snp | C/G | 0.156319 | 0.231784 | intron-variant | NSMAF | GRCh38.p7 | 8:58646035 | AACAAGAGCGAGACT[C/G]CGTCTCAAAATCATC | 8439 |
rs60504120 | snp | G/T | 0.157972 | 0.232445 | intron-variant | NSMAF | GRCh38.p7 | 8:58640868 | CACCACACCTGAACT[G/T]TTTCATTTTCTCTTT | 8439 |
rs60534391 | snp | A/T | 0.293551 | 0.246177 | intron-variant | NSMAF | GRCh38.p7 | 8:58606769 | CAGGCTTTCACCATG[A/T]ACTAGCTGGGAGCTT | 8439 |
rs60567264 | snp | A/C | 0.42357 | 0.179927 | intron-variant | NSMAF | GRCh38.p7 | 8:58655088 | AAGTGATCCACCCAC[A/C]TTGGCCTCCCAAAGT | 8439 |
rs60663073 | in-del | -/G | 0.110561 | 0.207501 | intron-variant | NSMAF | GRCh38.p7 | 8:58638458 | GCTGTACAGACCAAT[-/G]GAACACAATACATCC | 8439 |
rs60780937 | snp | C/T | 0.152001 | 0.229992 | intron-variant | NSMAF | GRCh38.p7 | 8:58596288 | CCAGGAAGCTATTTC[C/T]CCATGCTTGAGAGAA | 8439 |
rs61196735 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58592911 | CAAAAACAAAAACAA[-/C]AACAACAAAAAAAAA | 8439 |
rs61359641 | in-del | -/CT | 0.165853 | 0.235413 | intron-variant | NSMAF | GRCh38.p7 | 8:58598849 | CAACATGGTGAAACC[-/CT]GTCACGACCAAAAAA | 8439 |
rs61542378 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58631431 | AGATGTTAATAGAGT[C/T]ACAAAATTTTATTGT | 8439 |
rs61553196 | in-del | -/CA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58592917 | CAAAAACAACAACAA[-/CA]AAAAAAAAACCTCTC | 8439 |
rs62512000 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58643552 | TTTTTTTTTTTTTGG[G/T]ACGGAGTTTCACTCT | 8439 |
rs62512001 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58645112 | GAACTTAAAGTATAA[A/C/T]TAAAAAAAAAAAAAA | 8439 |
rs66472341 | in-del | -/AA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58601547 | TGTCTAGAATACAGA[-/AA]AAAAAAAAAAAAATA | 8439 |
rs67832316 | in-del | -/A | 0.431769 | 0.17164 | intron-variant | NSMAF | GRCh38.p7 | 8:58640556 | CAATATTGCAACTGG[-/A]AAAGTTTACAATTAC | 8439 |
rs67992430 | in-del | -/TAA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58600771 | CTCAGTGTGGTGGGA[-/TAA]TACCAAGTAAACTTA | 8439 |
rs71250204 | in-del | -/AAAAAAAAAAAAAA | 0.0209421 | 0.100162 | intron-variant | NSMAF | GRCh38.p7 | 8:58598491 | GACTCTGTCTCAAAC[-/AAAAAAAAAAAAAA]AAAAAAAGAAAAAAA | 8439 |
rs71521421 | snp | G/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58606919 | AGCACTTAATCAATG[G/T]TAATTTCTTCTCTTT | 8439 |
rs71521422 | snp | A/C | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58620051 | GATATAAGGCAATAA[A/C]CAAGTAAGAGAATGG | 8439 |
rs71521423 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58632352 | CATGACAGGTTTTCA[C/T]CCCTACCATATTATT | 8439 |
rs71767302 | in-del | -/T | 0.499539 | 0.0151687 | intron-variant | NSMAF | GRCh38.p7 | 8:58643535 | CTCTAGGGACAGATC[-/T]TTTTTTTTTTTTTTG | 8439 |
rs71942199 | in-del | -/AAA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58601558 | CAGAAAAAAAAAAAA[-/AAA]AATAGAGCTAAGTGT | 8439 |
rs72647443 | snp | A/G | 0.397994 | 0.201489 | intron-variant | NSMAF | GRCh38.p7 | 8:58584812 | TTTCTAATATTTCTG[A/G]TTTTTAGTAAGAGAT | 8439 |
rs72647444 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58591776 | ACAGGTGTGAGTAAC[C/T]GTGCCCGGCCTCAAA | 8439 |
rs72647445 | snp | A/T | 0.00835141 | 0.0640778 | intron-variant | NSMAF | GRCh38.p7 | 8:58595434 | TTTGGGGAGATTTTT[A/T]AAAATAAAGACAACA | 8439 |
rs72647450 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58608126 | TTAGTTTGGGGTGGG[G/T]TGATATCTTTCAGGT | 8439 |
rs72647451 | snp | A/C | 0.408017 | 0.193729 | intron-variant | NSMAF | GRCh38.p7 | 8:58610673 | AGTGAGTAAGGGCTG[A/C]AGAATGAAGAGAGAT | 8439 |
rs72647454 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMAF | GRCh38.p7 | 8:58624738 | CTGTTGGGTAGAAAG[C/T]TCTGCATATCTGTTA | 8439 |
rs72647462 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58649393 | ATGAGACTTAGGACT[C/T]TGGACTTGATGTTGA | 8439 |
rs72647463 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NSMAF | GRCh38.p7 | 8:58653159 | TGATTAGCTTCAGAT[C/T]TTAAATTTAATATGC | 8439 |
rs72647464 | snp | A/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58655506 | CTGGGCTCGAGTGAT[A/C]TTCCCACCTTTTAAT | 8439 |
rs73240230 | snp | A/T | 0.02016 | 0.0983543 | intron-variant | NSMAF | GRCh38.p7 | 8:58640236 | GAGGTGATGGATATG[A/T]TAATTACTTTGATTG | 8439 |
rs73240232 | snp | C/G | 0.0898077 | 0.191933 | intron-variant | NSMAF | GRCh38.p7 | 8:58641665 | GTCTCCTGTAGGATT[C/G]TTCCTAGTCTTTTAC | 8439 |
rs73240235 | snp | C/G | 0.111224 | 0.207945 | intron-variant | NSMAF | GRCh38.p7 | 8:58647542 | GGTGATTGGATCATG[C/G]GGGTAGATCCCTCAT | 8439 |
rs73240247 | snp | C/G | 0.117886 | 0.21224 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660504 | TTGTTGAGATAATTG[C/G]TCGCATGATTTTTTT | 8439 |
rs73240249 | snp | A/G | 0.0901694 | 0.192235 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660681 | CCATACCCTCTAGCT[A/G]TCACTCTTCCTAACT | 8439 |
rs73240250 | snp | A/G | 0.0944967 | 0.195752 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661030 | TGGACCTATGTTTCC[A/G]TTTCTGTTGAGTGGA | 8439 |
rs73240252 | snp | A/T | 0.0941369 | 0.195465 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661137 | CTTCTGATTGACCCC[A/T]GTTCTGGGAAGGCCT | 8439 |
rs73248892 | snp | G/T | 0.0314385 | 0.121371 | intron-variant | NSMAF | GRCh38.p7 | 8:58592940 | AAACCTCTCTCTCCT[G/T]TATTGTGAAAATCCA | 8439 |
rs73248900 | snp | C/T | 0.0376037 | 0.131863 | intron-variant | NSMAF | GRCh38.p7 | 8:58594412 | TCACAGCATGTCTGC[C/T]GGATCTGTCCCAGCA | 8439 |
rs73248901 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NSMAF | GRCh38.p7 | 8:58594595 | CTTCTATTCCCCCTC[A/G]TTTGACCATCACCAA | 8439 |
rs73250303 | snp | C/T | 0.114738 | 0.210248 | intron-variant | NSMAF | GRCh38.p7 | 8:58594796 | GAGAAAAGACAGCCA[C/T]TGTCATCATGAATCA | 8439 |
rs73250333 | snp | A/G | 0.0998734 | 0.199905 | intron-variant | NSMAF | GRCh38.p7 | 8:58615150 | TTAAGAAGACATTAC[A/G]CATCTTAATGTATAT | 8439 |
rs73250335 | snp | C/G | 0.149665 | 0.228982 | intron-variant | NSMAF | GRCh38.p7 | 8:58615753 | GGTGACCTAGACTTT[C/G]TTCTTAGAAAGTTAC | 8439 |
rs73250339 | snp | C/T | 0.097727 | 0.198275 | intron-variant | NSMAF | GRCh38.p7 | 8:58617087 | TTGGTCTGTTCTTCT[C/T]AAATCTACAATCATT | 8439 |
rs73250343 | snp | C/T | 0.147656 | 0.228091 | intron-variant | NSMAF | GRCh38.p7 | 8:58618815 | AACAAAAAATTATCT[C/T]CTCAGAAATACGATG | 8439 |
rs73250346 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58625755 | CACTCCATATTTTTT[G/T]ATTGGGGAGTTTGAT | 8439 |
rs73250347 | snp | A/T | 0.109108 | 0.206518 | intron-variant | NSMAF | GRCh38.p7 | 8:58626645 | TTCATATTTTTGCAA[A/T]TGCAAATTGTGTTAC | 8439 |
rs73250349 | snp | A/T | 0.0901694 | 0.192235 | intron-variant | NSMAF | GRCh38.p7 | 8:58626673 | TACTATAACTATGTG[A/T]GTGCATGTGTCTTGT | 8439 |
rs73250352 | snp | C/G | 0.0718919 | 0.175435 | intron-variant | NSMAF | GRCh38.p7 | 8:58627059 | TTGATGGGATTATTT[C/G]TTTTTTGCTTGCTGA | 8439 |
rs73250359 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58630398 | TTTACTCAGACAACC[G/T]CACTTTTATTTCCTT | 8439 |
rs73250362 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58631347 | AAAATCTGTGGCTCC[C/T]TTGGGTAATTTTGTT | 8439 |
rs73684346 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58595313 | GACCACATCTTGTAC[C/T]GTGAAGTGACAGACT | 8439 |
rs73684347 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58601608 | GACAAGTAGAAAAAG[C/T]CTAAAAGAAATCATA | 8439 |
rs73684348 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | NSMAF | GRCh38.p7 | 8:58605161 | CTTGAACATCATAAT[A/G]TAAGTATTTTCTCTG | 8439 |
rs73684352 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58631852 | AAGCAGACAGGGAAG[A/G]AGGCTAATCCAAGTG | 8439 |
rs73684353 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58636257 | ATAACCCCCTGGGAC[C/T]CTGCTGAATAACACA | 8439 |
rs74356313 | snp | A/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58619950 | GGGGCCCTGCACTAC[A/C]AGATATCAATAGTTA | 8439 |
rs74378476 | snp | A/G | 0.0448719 | 0.142907 | intron-variant | NSMAF | GRCh38.p7 | 8:58657494 | TGATGCAAGGGGATA[A/G]ACCCGGAAAAATCTG | 8439 |
rs74390016 | snp | A/G | 0.0327778 | 0.123752 | intron-variant | NSMAF | GRCh38.p7 | 8:58655288 | AGTATCTAAACTTCT[A/G]CATTACCCAAGAAAT | 8439 |
rs74411351 | snp | A/C | 0.177503 | 0.239258 | intron-variant | NSMAF | GRCh38.p7 | 8:58655895 | CTGGGCGAGAGTGAG[A/C]CTCCGTCTCAATAAA | 8439 |
rs74444047 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | NSMAF | GRCh38.p7 | 8:58586209 | TTGATTATGAGTTCA[C/T]TTTTATCTTAAATTA | 8439 |
rs74566438 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | NSMAF | GRCh38.p7 | 8:58596428 | TGGAAGCCTGTAGGT[C/T]TGAAGTTGTCTTAGG | 8439 |
rs74639699 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | NSMAF | GRCh38.p7 | 8:58647912 | GGATATACGTAAAGA[C/T]ATGGAAGCAGCTTTG | 8439 |
rs74675746 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58638839 | TCAAAAGACAACCTA[C/T]GGAATGGGAGAAAAT | 8439 |
rs74784575 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58647738 | GCTTACCAGAAACCA[A/G]GCAGATGCTGGTGCC | 8439 |
rs74799426 | snp | A/T | 0.0333695 | 0.124785 | intron-variant | NSMAF | GRCh38.p7 | 8:58646561 | GAAGGGATATAACCA[A/T]ATCATATTGTTTGAA | 8439 |
rs74802209 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | NSMAF | GRCh38.p7 | 8:58648772 | GTGTTAGGTGTGCAG[A/G]TGCACAGAATGCAAG | 8439 |
rs74805916 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58645128 | TAAAAAAAAAAAAAA[A/G]AGAAATTGCAGTATC | 8439 |
rs74853108 | snp | G/T | 0.155656 | 0.231515 | intron-variant | NSMAF | GRCh38.p7 | 8:58636694 | CAGCCACACACAGTA[G/T]GTACACAAATGGGAA | 8439 |
rs74931651 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58637797 | AAATTTAACCAAGGA[G/T]GTAAAAAGTCTGTAC | 8439 |
rs74972994 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58643851 | TCTTTAGATATTCCC[C/T]TGTGATAACCAGCCC | 8439 |
rs74999856 | snp | A/G | 0.133093 | 0.220981 | intron-variant | NSMAF | GRCh38.p7 | 8:58629457 | AATTTTCCTGAGCTC[A/G]TTAAGCATCTTTATG | 8439 |
rs75030081 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58602433 | TTCCAAGTAAAACAA[C/G]AACAACAACAAAATT | 8439 |
rs75109800 | snp | A/G | 0.00923794 | 0.0673322 | intron-variant | NSMAF | GRCh38.p7 | 8:58635240 | CCTAAAATACAGATA[A/G]AAGTCATTAAATATA | 8439 |
rs75227414 | snp | A/T | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58640336 | TATTCATCAATTATA[A/T]CTCAATAAAGCTGGA | 8439 |
rs75264318 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58601967 | CTGGTATAATTCCCC[C/T]AAGCCTTGGAGAAAC | 8439 |
rs75266299 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58649233 | GGGTTTCAGACTTCA[A/G]TGAGGCCTACTGCCC | 8439 |
rs75330784 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58617014 | AGATGGCAGCATCTA[C/T]ATACTAAACAGAACA | 8439 |
rs75450902 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58587118 | CAGTACTGTCAACTA[C/T]AGCATAAGATGCAGC | 8439 |
rs75471338 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58609328 | ATCTCTAGCGACCCT[C/T]TACTAAAATAGGGAG | 8439 |
rs75517496 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | NSMAF | GRCh38.p7 | 8:58611772 | AAAAAATATATAGGA[A/G]TGTGTATCTGAGATC | 8439 |
rs75535763 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | NSMAF | GRCh38.p7 | 8:58612355 | TGAAGACATCTATGT[A/G]CCAGGAGGGTGATGT | 8439 |
rs75546621 | snp | A/T | 0.00716266 | 0.059414 | intron-variant | NSMAF | GRCh38.p7 | 8:58596185 | AGAGTGCAGTTTGAA[A/T]CAGCATCACAAGATA | 8439 |
rs75646495 | snp | A/C | 0.444444 | 0.157135 | intron-variant | NSMAF | GRCh38.p7 | 8:58637042 | CACACACACACACAC[A/C]CACACACAAACACAC | 8439 |
rs75647812 | snp | C/T | 0.175897 | 0.238765 | intron-variant | NSMAF | GRCh38.p7 | 8:58657952 | TACAGGTTTCAAGGT[C/T]TGTGTGACACCACGG | 8439 |
rs75669640 | snp | C/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58596952 | AAAAAAAAAAAAGAT[C/G]TGTATGTGGGTATAG | 8439 |
rs75712986 | snp | C/T | 0.0441095 | 0.141807 | intron-variant | NSMAF | GRCh38.p7 | 8:58637233 | TTGATACCTTCCTTA[C/T]TTGCCAGTATGACAG | 8439 |
rs75717007 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58634597 | AAGCAGATGAAACCC[A/T]GAGCCAAAAGAAAGT | 8439 |
rs75763165 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | NSMAF | GRCh38.p7 | 8:58624903 | AGTTCTATCAATGTT[C/T]GCTTCATATATTTAG | 8439 |
rs75794523 | snp | A/G | 0.121022 | 0.21416 | intron-variant | NSMAF | GRCh38.p7 | 8:58625813 | TACTGTTGCCATTTT[A/G]ACTGTTTTCTGTCTT | 8439 |
rs75827935 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | NSMAF | GRCh38.p7 | 8:58651438 | TCAGCTGGACTCTAG[A/G]AAATTACATTCTCCC | 8439 |
rs75851323 | snp | C/G | 0.0329836 | 0.124112 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660813 | GGCCTTTTGTGTCTG[C/G]CTTCTTTCATTTAGC | 8439 |
rs75868612 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | NSMAF | GRCh38.p7 | 8:58592307 | CATTTCTCAGTCAGG[A/G]AACCAAAAAAATGGA | 8439 |
rs75916717 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58620228 | CAGGAAAGACCTTCT[A/G]GAAGAACTGAGAGCA | 8439 |
rs75989158 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58638580 | TAGATATCCCCGTGG[A/G]AAAAAAAAAGTGAAC | 8439 |
rs76002125 | snp | A/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58645114 | ACTTAAAGTATAATT[A/T]AAAAAAAAAAAAAAA | 8439 |
rs76043179 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58592181 | TTTAAGATGATTAAT[C/T]TGAGACATCCTACAA | 8439 |
rs76050509 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58608992 | ACAAGTTTCAGCATG[A/G]ATATCTAAGTTTATA | 8439 |
rs76103962 | snp | A/G | 0.095934 | 0.196885 | intron-variant | NSMAF | GRCh38.p7 | 8:58625418 | TATGTATGTATGTAT[A/G]TATATGTGTGAATGT | 8439 |
rs76129781 | in-del | -/GT | 0.177824 | 0.239355 | intron-variant | NSMAF | GRCh38.p7 | 8:58656024 | TCTAAATCTTTTTTT[-/GT]TTTGTTTGTTTGAGA | 8439 |
rs76143633 | snp | A/C | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58596932 | CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA | 8439 |
rs76143792 | snp | G/T | 0.0329836 | 0.124112 | intron-variant | NSMAF | GRCh38.p7 | 8:58610640 | TGAGTGGCAGGAGGA[G/T]GAGCAACCTATGATA | 8439 |
rs76189774 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58636386 | AGAAATTAATAATTC[C/T]TTAATGTCATCATGT | 8439 |
rs76262616 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | NSMAF | GRCh38.p7 | 8:58635930 | TGTTCTTTTGTGAGC[A/G]GTAAATATTTACTTT | 8439 |
rs76279588 | snp | A/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58596951 | AAAAAAAAAAAAAGA[A/T]CTGTATGTGGGTATA | 8439 |
rs76301119 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | NSMAF | GRCh38.p7 | 8:58630321 | TCCACCTCACCCTTT[C/T]TTTTTTTTTAATCTG | 8439 |
rs76354168 | snp | A/T | 0.0917425 | 0.193579 | intron-variant | NSMAF | GRCh38.p7 | 8:58585855 | GAAGTGATCATGAAC[A/T]TGTCTGTAAATGTCT | 8439 |
rs76433721 | snp | A/C | 0.0244538 | 0.107838 | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58583817 | ATTTATCTCTTAGCT[A/C]TTCTCTGCTACTTAG | 8439 |
rs76522931 | snp | A/G | 0.125182 | 0.216612 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661736 | AGAGAGAGAGACCTT[A/G]TCTCAAAAGAAAAAA | 8439 |
rs76548657 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58643481 | TGCCCCCAACATCTG[C/T]CTCATGGTTATCTGA | 8439 |
rs76568131 | snp | A/T | 0.0569829 | 0.158885 | intron-variant | NSMAF | GRCh38.p7 | 8:58653498 | ACAATGGAAAATCCC[A/T]TACAAAGCAAATAAC | 8439 |
rs76597186 | snp | A/G | 0.119387 | 0.213167 | intron-variant | NSMAF | GRCh38.p7 | 8:58635551 | CTCTGATTTTCCTAG[A/G]GATCCAAGTACAACA | 8439 |
rs76620947 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | NSMAF | GRCh38.p7 | 8:58652922 | AGAGAAAATAATTCC[A/G]TAACGAGGATATGAC | 8439 |
rs76664593 | snp | A/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58658926 | TCCAACACAAGGTCC[A/T]CTGCGCGGGGAGCAA | 8439 |
rs76751509 | snp | A/C | 0.183568 | 0.241012 | intron-variant | NSMAF | GRCh38.p7 | 8:58604379 | TCTTTTTATTGTAAT[A/C]TTGTTATAGTTAAAA | 8439 |
rs76766121 | snp | A/C | 0.000747803 | 0.0193221 | intron-variant | NSMAF | GRCh38.p7 | 8:58640141 | TGACTACAGTCCATA[A/C]CACATCATACACTTG | 8439 |
rs76775419 | snp | C/G | 0.0337553 | 0.125452 | intron-variant | NSMAF | GRCh38.p7 | 8:58651336 | CTTCCCTCCCAGAAA[C/G]AGTTCTCATGAATTT | 8439 |
rs76795096 | snp | G/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58627766 | GGTCATTTTCACAAT[G/T]TTGAGTCTACCCATC | 8439 |
rs76812722 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58607701 | CCATAAGTGTTTACC[A/G]TCAATAAACTGCTGG | 8439 |
rs76937541 | snp | C/T | 0.0418186 | 0.138422 | intron-variant | NSMAF | GRCh38.p7 | 8:58616880 | TGAATTTAGAAGAGT[C/T]ATAGTATACAAGGCC | 8439 |
rs77029767 | snp | A/C/T | 0.0422008 | 0.138995 | intron-variant | NSMAF | GRCh38.p7 | 8:58651757 | ATTACTGTTATCTAG[A/C/T]GCAGCGCTTCACAAA | 8439 |
rs77059535 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | NSMAF | GRCh38.p7 | 8:58657714 | CATGGGGCAGAGCAC[G/T]AAACAATTTGGGCAC | 8439 |
rs77125463 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58650256 | ACTTCCTAGTTCCAA[A/G]GGCAACTTTGGAAGT | 8439 |
rs77192980 | snp | C/T | 0.0558544 | 0.157504 | intron-variant | NSMAF | GRCh38.p7 | 8:58593123 | AAAGATAAAGCACTT[C/T]GTCTGAGGCTATAAT | 8439 |
rs77219624 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58636712 | ACACAAATGGGAATG[C/G]CTGTGTTCCAGTAAA | 8439 |
rs77564282 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58647359 | TCTGAAATAAAGAAG[A/G]AATTAAGAAAACTGT | 8439 |
rs77593073 | snp | A/G | 0.079617 | 0.182947 | intron-variant | NSMAF | GRCh38.p7 | 8:58594566 | CAATTTCTGGCAATT[A/G]GAAAACTCTTCTCCT | 8439 |
rs77608120 | snp | A/G | 0.289942 | 0.246789 | intron-variant | NSMAF | GRCh38.p7 | 8:58605893 | TCCAAAAAAAAAAAA[A/G]AAAGAAAGAAACAAT | 8439 |
rs77620684 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58637608 | ACCCTAAGGATTCTA[C/T]CAAAAAAACTATTCA | 8439 |
rs77724289 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58650934 | AGCCACCATTTCTTC[C/T]ACCCACTTAACGTGG | 8439 |
rs77736827 | snp | C/T | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58598849 | CCAACATGGTGAAAC[C/T]GTCACGACCAAAAAA | 8439 |
rs77754084 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58645204 | GTGAATGAGGGCAGT[A/G]GCCCCCAATTCTTTT | 8439 |
rs77805388 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | NSMAF | GRCh38.p7 | 8:58634941 | TTCATTTCAAGCCTC[A/G]TAAATCATAAATCGT | 8439 |
rs77807250 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58642210 | GAATAATAAAAATAA[A/G]TGGATTTATCTACTG | 8439 |
rs77940965 | snp | C/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58607930 | GGGAAAAAAAAATCA[C/G]CAAATCTTGCTTTCC | 8439 |
rs77949515 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | NSMAF | GRCh38.p7 | 8:58655303 | ACATTACCCAAGAAA[C/T]AGCTGTCATCCCAAC | 8439 |
rs77976156 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58641387 | CCTCATTCCATCTCT[A/C]TATTGTTCTTCTGAT | 8439 |
rs77982702 | snp | C/G | 0.0584853 | 0.160693 | intron-variant | NSMAF | GRCh38.p7 | 8:58630970 | TCTACTATGTATTAA[C/G]CTGAAGCATAAAGAA | 8439 |
rs77985891 | snp | A/G | 0.0799831 | 0.183287 | intron-variant | NSMAF | GRCh38.p7 | 8:58593675 | AACAATGGTGTATAT[A/G]GTAAGGGATGCTTTC | 8439 |
rs78073005 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660522 | GCATGATTTTTTTTT[A/T]TATAACAGCTTTATT | 8439 |
rs78087465 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58640592 | ATTCTTTTTCAACTT[C/G]TTTGCAATACTTTTT | 8439 |
rs78100978 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58652244 | AGAGATTACCTACAA[A/G]GAACAATTAGACTTA | 8439 |
rs78187905 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58641788 | AGATCAATAGGTTAA[A/T]GCACATGTCATCTTA | 8439 |
rs78203934 | snp | A/C | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58605879 | AGCGAGACTCAGCCT[A/C]CAAAAAAAAAAAAAA | 8439 |
rs78232690 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58644020 | TTGTTGTATGGCTAC[A/G]GCAACAAATACATGA | 8439 |
rs78267912 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58639917 | TACTACATGATTTCA[C/T]GTAGACTCTAAAAGA | 8439 |
rs78283377 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58646390 | ATTTTATTTCTATGA[C/T]GCACAAGTAGCCTTC | 8439 |
rs78313259 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | NSMAF | GRCh38.p7 | 8:58630380 | GGAACAAAAGAGCTT[C/T]TCTTTACTCAGACAA | 8439 |
rs78320292 | snp | A/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58639288 | GACTCCGTCTCAATA[A/T]AAAAAAAAAAAGAAG | 8439 |
rs78351859 | snp | G/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58651217 | AAAAGACCTGGCTCA[G/T]TTTATTATCCATGTT | 8439 |
rs78387563 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | NSMAF | GRCh38.p7 | 8:58652958 | AGAAGGAATATTGAA[C/T]AAAAACAATGGTAAA | 8439 |
rs78517028 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58620501 | ACTGGGGATGGGGGC[A/G]TCTTGAAAATTTTTA | 8439 |
rs78533823 | snp | A/T | 0.0995161 | 0.199636 | intron-variant | NSMAF | GRCh38.p7 | 8:58658208 | GTACTAAACAAAGAA[A/T]CTCCACTCAAGCTCT | 8439 |
rs78576678 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMAF | GRCh38.p7 | 8:58610707 | CAGGGAAATGGAAAG[C/T]CAGAGTTGAGACTGG | 8439 |
rs78609537 | snp | A/C | | | synonymous-codon | NSMAF | GRCh38.p7 | 8:58601494 | GGAAGAGTAGTGACT[A/C]CCATACATGAACTTT | 8439 |
rs78629641 | snp | A/C | 0.031825 | 0.122064 | intron-variant | NSMAF | GRCh38.p7 | 8:58603110 | AATTTGTTCACATGT[A/C]ACATCACAATTATAA | 8439 |
rs78674858 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | NSMAF | GRCh38.p7 | 8:58642482 | CTTCTAGTTCAAATC[A/G]CATGACTCATTTTGA | 8439 |
rs78681369 | snp | A/G | 0.120674 | 0.21395 | intron-variant | NSMAF | GRCh38.p7 | 8:58634516 | AATTCTTCTCTGAAC[A/G]CTTCAACACCCCAAG | 8439 |
rs78734696 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | NSMAF | GRCh38.p7 | 8:58658624 | CACTGGAAGATCTGT[A/G]GCTCTCACAATCAAA | 8439 |
rs78831721 | snp | C/T | 0.0528381 | 0.153711 | intron-variant | NSMAF | GRCh38.p7 | 8:58658060 | TGTATATCAAAAAGG[C/T]CAATATGAGTATTGG | 8439 |
rs78848156 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | NSMAF | GRCh38.p7 | 8:58648940 | GCTGGAGTCCCCATA[C/T]ATAGTCCCCACCAAG | 8439 |
rs78976045 | snp | A/G | 0.0573587 | 0.15934 | intron-variant | NSMAF | GRCh38.p7 | 8:58653084 | CTATAACTGAGGATG[A/G]GGGCACAGCAGTTAA | 8439 |
rs79040519 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58638620 | ATCCCATACATAAAA[A/G]TCTACTTGAAATGAA | 8439 |
rs79040985 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NSMAF | GRCh38.p7 | 8:58648192 | GGGATCTGTGGAAGG[C/T]TGAACTTAAGAGTAA | 8439 |
rs79046832 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | NSMAF | GRCh38.p7 | 8:58628431 | AGTCACATACAAAAA[A/C]TATTCCTTCAGATAC | 8439 |
rs79075701 | snp | A/G | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58636353 | TCTTAATAAGTGACC[A/G]ATCATTAACACACTC | 8439 |
rs79085330 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58587105 | CTTAGAGAAAAGGCA[A/G]TACTGTCAACTACAG | 8439 |
rs79088831 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58647789 | AGAACCATGAGCCAA[C/T]TAAGCCTCTTTCCAT | 8439 |
rs79089199 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58629888 | CCTTTGAAGCAGTAG[C/T]GTGCTACCCAGCTCT | 8439 |
rs79263920 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58625515 | TATCTTTCTGATAAA[C/T]TGACCCTTTTATCAT | 8439 |
rs79270027 | snp | A/G | 0.118235 | 0.212457 | intron-variant | NSMAF | GRCh38.p7 | 8:58635875 | ATAGTCTTACAGACT[A/G]AGAATGCCTACACTC | 8439 |
rs79339869 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | NSMAF | GRCh38.p7 | 8:58590657 | TCCAAGTATTTTAAG[A/C]TAAAAATGAAATCAC | 8439 |
rs79496598 | snp | A/G | 0.0603597 | 0.1629 | intron-variant | NSMAF | GRCh38.p7 | 8:58648908 | GTCTACGACAGTAGT[A/G]TGAAGGGGAAAAGTG | 8439 |
rs79518213 | snp | C/T | | | missense | NSMAF | GRCh38.p7 | 8:58623391 | CCATGGCGGTTTGGT[C/T]ACCCAATTTGTCAAG | 8439 |
rs79542143 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | NSMAF | GRCh38.p7 | 8:58603831 | TAGGCTTGGAAGAGA[G/T]GTACTACTGCTAATT | 8439 |
rs79546377 | snp | A/G | 0.0329836 | 0.124112 | intron-variant | NSMAF | GRCh38.p7 | 8:58616876 | TGAGTGAATTTAGAA[A/G]AGTCATAGTATACAA | 8439 |
rs79584150 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NSMAF | GRCh38.p7 | 8:58596430 | GAAGCCTGTAGGTTT[C/G]AAGTTGTCTTAGGTA | 8439 |
rs79668053 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | NSMAF | GRCh38.p7 | 8:58593592 | AGAGTGCCAACACAG[C/T]GCTCTCAACATGACA | 8439 |
rs79697297 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | NSMAF | GRCh38.p7 | 8:58625614 | CTAGCTCTGTTGTTT[C/G]ATTACCAAGCATGGA | 8439 |
rs79745047 | snp | C/T | 0.16846 | 0.236329 | intron-variant | NSMAF | GRCh38.p7 | 8:58591893 | TTCTAACTTACACAA[C/T]GTGATGTCGGAATGA | 8439 |
rs79745296 | snp | C/G | 0.0799831 | 0.183287 | intron-variant | NSMAF | GRCh38.p7 | 8:58593936 | CCAACAAGTGGACAG[C/G]GCACCTCTCATGGGC | 8439 |
rs79758009 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | NSMAF | GRCh38.p7 | 8:58632569 | CTTCCGTCTACTTTT[G/T]GACCTTGCTTTGTTC | 8439 |
rs79764090 | snp | G/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58591507 | TTTTTTTTTTTTTTT[G/T]ACACAGTATCACTCT | 8439 |
rs79799797 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58646993 | TGTACAACACTTAAC[C/T]AGAACTTAAAATAGC | 8439 |
rs79806631 | snp | A/G/T | 0.00776208 | 0.0618133 | intron-variant | NSMAF | GRCh38.p7 | 8:58586049 | CAGCTTCAGAATGTG[A/G/T]TTTACATTATTCTGG | 8439 |
rs79878854 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58641836 | CACCTACATGGGGCT[A/G]TACCATTTTGCCCTA | 8439 |
rs79989266 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | NSMAF | GRCh38.p7 | 8:58631777 | ACAAGATAGCAACAA[A/T]TACAAGATAAATAAA | 8439 |
rs80127104 | snp | A/C | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58637038 | CACACACACACACAC[A/C]CACCCACACACAAAC | 8439 |
rs80127371 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58658448 | TGGACACACTGGTTA[C/G]ACCAACATTACAGAT | 8439 |
rs80145292 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58655400 | TAAAATAGAAATGTC[C/T]TTTTTTTTTTTTTCT | 8439 |
rs80347765 | snp | A/C/G | 0.0422008 | 0.138995 | intron-variant | NSMAF | GRCh38.p7 | 8:58651797 | GCACACAATCAACTG[A/C/G]GGATCTTGTTAAAAT | 8439 |
rs111250614 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58585590 | TGTTCCCTGATGGAA[A/G]AGGCAGGCTTGAGTT | 8439 |
rs111266642 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58646022 | CTCCAGCCTAGGCAA[A/C]AAGAGCGAGACTCCG | 8439 |
rs111319005 | snp | A/G | 0.00522792 | 0.0508589 | missense | NSMAF | GRCh38.p7 | 8:58603374 | TCAGCAGTGTGCTCC[A/G]CCACATGGTGCTCTG | 8439 |
rs111348885 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58648460 | CTATGGAATAATTGC[A/G]TGCTAGAGAGATGAG | 8439 |
rs111374814 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58645468 | AACTAAACAGCCTCA[C/G]AGAAAAAGCCAGGTC | 8439 |
rs111387497 | snp | C/T | 0.130008 | 0.219321 | intron-variant | NSMAF | GRCh38.p7 | 8:58598987 | GCCAAGATTGTGTCA[C/T]TGCACTCCAGCCTGG | 8439 |
rs111446513 | in-del | -/C | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58589722 | CTCAAATTACTAAAT[-/C]AAAATATTCAAAATT | 8439 |
rs111479963 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | NSMAF | GRCh38.p7 | 8:58607108 | ATTCCACAATGCTTT[C/T]GTAATGTCACCAAGT | 8439 |
rs111495601 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58601172 | AGATAGAACAATTAG[C/T]GATTTTTTACATTTC | 8439 |
rs111503399 | in-del | -/AA | 0.5 | 0 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660099 | GTGTCCTCCATTGTG[-/AA]AAAAAAAAAAAAAGA | 8439 |
rs111510937 | snp | C/T | 0.0236746 | 0.106192 | intron-variant | NSMAF | GRCh38.p7 | 8:58593544 | CATGGAAGCAGGAAG[C/T]AAAGATACTACCCTT | 8439 |
rs111515165 | snp | A/T | 0.125182 | 0.216612 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661451 | AAAATAAAAATTACC[A/T]GGGTACAGTGGCACA | 8439 |
rs111516405 | in-del | -/TG | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58625416 | GTATGTATGTATGTA[-/TG]TATATATGTGTGAAT | 8439 |
rs111524143 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | NSMAF | GRCh38.p7 | 8:58589722 | CTCAAATTACTAAAT[A/C]AAAATATTCAAAATT | 8439 |
rs111526931 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58624127 | GCTCACTGCAACCTC[C/T]GTCTCCTGGGTTCAA | 8439 |
rs111551809 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | NSMAF | GRCh38.p7 | 8:58600452 | ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATA | 8439 |
rs111561052 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58654340 | TGGCTCACCTGAGAT[A/C]GGGAGTTCGAGACCA | 8439 |
rs111601968 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58594554 | ACATATTCCTGACAA[C/T]TTCTGGCAATTGGAA | 8439 |
rs111613231 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58617610 | TCAAAACCACAACAA[A/G]ATACCATCTCATGCC | 8439 |
rs111629575 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58657650 | CTGTCATTCAAATGC[A/G]TATTCTATGCATTGA | 8439 |
rs111725014 | snp | A/G | 0.5 | 0 | missense | NSMAF | GRCh38.p7 | 8:58599833 | TTCAGGCTATTGACT[A/G]GAAAGCTCACATCAT | 8439 |
rs111780262 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58603849 | ACTACTGCTAATTTG[G/T]CAATGACTACATATT | 8439 |
rs111791325 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SDCBP, NSMAF | GRCh38.p7 | 8:58583009 | GCTGAGACTGAGTGT[C/T]AGGAAAATTGCTTCC | 8439 |
rs111825363 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58607992 | CAAGGTGATATCTGG[C/T]TTCCCATTCTGCTCT | 8439 |
rs111935811 | snp | A/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58608572 | AGGATCCTGGCCAGT[A/T]TTGGGAAGGGGTAAA | 8439 |
rs112104200 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NSMAF | GRCh38.p7 | 8:58601799 | TTTATGTGTCTCTTA[C/T]GCGATTTACCACAGA | 8439 |
rs112124743 | snp | G/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58601185 | AGTGATTTTTTACAT[G/T]TCTTTACTTTTTTAT | 8439 |
rs112174205 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58655358 | AAAAATTTAACAATT[C/T]GCCTACTTTAGTCTA | 8439 |
rs112174664 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58596804 | GTGGTGGCGGGCGCC[G/T]GTAGTCCCAGCTACT | 8439 |
rs112213500 | in-del | -/A | 0.415563 | 0.18732 | intron-variant | NSMAF | GRCh38.p7 | 8:58645266 | GTGGTTTTTCTATTT[-/A]AAAAAAAAGTGGAAC | 8439 |
rs112226247 | in-del | -/TCTTTAAATAATT | 0.0103295 | 0.0711199 | intron-variant | NSMAF | GRCh38.p7 | 8:58591909 | GTGATGTCGGAATGA[-/TCTTTAAATAATT]TCTTCTGCACAGTAT | 8439 |
rs112228649 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58610578 | GTTGAGCATGTAAAG[C/T]AACCTAAATGAACAT | 8439 |
rs112233809 | snp | A/T | | | splice-acceptor-variant | NSMAF | GRCh38.p7 | 8:58601537 | TCCTGGTAGCGTGTC[A/T]AGAATACAGAAAAAA | 8439 |
rs112251427 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58657099 | ACCTGTCAATCACAC[A/G]TCCTAAAAACATCTA | 8439 |
rs112260176 | snp | G/T | 0.0146672 | 0.084371 | intron-variant | NSMAF | GRCh38.p7 | 8:58653635 | GATAACAATTCTAAG[G/T]TACTTACTGAATACA | 8439 |
rs112333009 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58637528 | AAAAGAAAGAACAGG[C/G]ATCCAAATTGGAAAA | 8439 |
rs112410678 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58600025 | GTTTCTGCAATACTA[C/T]ATATGAAAAAAAAAT | 8439 |
rs112436112 | snp | A/G | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58584523 | GACAAAAGTTGGGAG[A/G]CAGATGTGAAGGAAA | 8439 |
rs112471698 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58657331 | AATTAGCATGAGAGC[C/T]GCCAGTGAACTTACA | 8439 |
rs112500913 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58653609 | TGATAAAAAATTCAA[C/T]TCACCAAGAAGATAA | 8439 |
rs112518043 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58590238 | TAATTCCAGCTGTAG[A/G]GTTTTTTCCCAAATG | 8439 |
rs112550046 | in-del | -/CG | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58623300 | ACCAGAAAAAAAGTA[-/CG]TTTATAAGTATTTAT | 8439 |
rs112561291 | in-del | -/C | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58590305 | GACCTAGCCTGATGA[-/C]TCTCCAGGGTCCTGC | 8439 |
rs112563457 | snp | C/T | 0.0287284 | 0.116357 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661607 | GGGTGCAGTGGCACA[C/T]ACCTATAGTCCCAGC | 8439 |
rs112566612 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | NSMAF | GRCh38.p7 | 8:58653944 | AAGTAAGTGGGTAGG[C/T]TAGTAATACATTTTG | 8439 |
rs112601288 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58648574 | TCCCATCACAGAGGG[C/T]CTAGGAGAGGAAAGA | 8439 |
rs112613718 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58657531 | AATGGTAAATTTGGG[C/G]CTTAATAAAGTTGCC | 8439 |
rs112618535 | snp | A/C | 0.125182 | 0.216612 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661370 | TGAAGCTGGAGGATT[A/C]CTTGAAGCCAGGAGT | 8439 |
rs112763617 | snp | A/C | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58615254 | GACAATTTTAACATC[A/C]TTCTCTCAGTGACTG | 8439 |
rs112773679 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58654037 | TGTTTTTCATGTGAG[A/G]AAAAAAAACCCTATT | 8439 |
rs112819868 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | NSMAF | GRCh38.p7 | 8:58617518 | TATGAACAGACACTT[A/C]TCAAAAGAAGACATC | 8439 |
rs112934124 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58607472 | GTTTTACACAGATCA[C/T]TCTAGCCTGAGCCCA | 8439 |
rs112957608 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58586278 | TTTCTACCTGATACA[A/C/G]ATGCCACAAGTATAC | 8439 |
rs112972156 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58627321 | AGACAAGGTTACCCA[C/G]TTTCACCACTTCTAT | 8439 |
rs113021646 | snp | A/G/T | 0.000297 | 0.0121824 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58599239 | TTACATACCATTATG[A/G/T]GCCCCAACTGCATCA | 8439 |
rs113043285 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58613151 | GACTAGAAATTATAA[A/G]CATCTAAATATCTAA | 8439 |
rs113047690 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58654580 | GAAAGAAAGTTAATA[C/T]TAGCATAATCAAGAA | 8439 |
rs113053323 | snp | C/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58621233 | ATTAATTTGCTCCAG[C/T]GCCATCCGTGGCCTC | 8439 |
rs113075924 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58594413 | CACAGCATGTCTGCC[A/G]GATCTGTCCCAGCAT | 8439 |
rs113081985 | snp | A/C | 0 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58591600 | CAAGCAATTCTTGTG[A/C]CTCAGCCTCCCGAAT | 8439 |
rs113085598 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | NSMAF | GRCh38.p7 | 8:58600585 | GAGATTCTGCTCACT[A/G]TACTCCAGCCTGGGC | 8439 |
rs113098396 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58604758 | TTTGTTTGTTTGTTT[G/T]TTTGAGACAGGGTCT | 8439 |
rs113201208 | snp | A/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58589229 | TATAAATAATATATA[A/T]ATATATATTATAGAT | 8439 |
rs113211945 | snp | C/T | 0.105214 | 0.203807 | intron-variant | NSMAF | GRCh38.p7 | 8:58645972 | CTTGAACCTGGGAAG[C/T]AGAGGTTGCAGTGAG | 8439 |
rs113231777 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58641109 | GTATTTTAGCAGAGA[C/T]GAGGTTTCACCGTGT | 8439 |
rs113232919 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58594134 | ACTTTATGTGGAGGC[A/G]GCACATGCAAGTGCA | 8439 |
rs113332653 | snp | A/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58611180 | AGAGAAAAGACTCTA[A/T]AGAAGGTGTGTCAGA | 8439 |
rs113346339 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NSMAF | GRCh38.p7 | 8:58598824 | GGTCAGGAGTTTGAG[A/G]CCAACCTGGCCAACA | 8439 |
rs113368984 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMAF | GRCh38.p7 | 8:58597298 | CTCTAAGTAGCACAA[C/T]AGTATACGTCTTATC | 8439 |
rs113426123 | snp | A/C | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58656404 | TATTTATAAACATCA[A/C]CAATAAATGGCACCA | 8439 |
rs113439667 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58641616 | CTGCATAGTACTCCA[C/T]CATGTGGCCATTTCT | 8439 |
rs113440553 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58619641 | TTGCATTCTATATAT[A/C]AACAATAAACAGAAA | 8439 |
rs113493388 | snp | A/C/G | 3.30355e-05 | 0.00406407 | missense | NSMAF | GRCh38.p7 | 8:58609693 | GCGTCACCATTTCTG[A/C/G]TTTGCATTCCATGTG | 8439 |
rs113530938 | in-del | -/T | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58630318 | CATTCCACCTCACCC[-/T]TTTTTTTTTTTTAAT | 8439 |
rs113612498 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58609322 | GTCTAAATCTCTAGC[A/G]ACCCTTTACTAAAAT | 8439 |
rs113703391 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58639241 | GTGAGCAGAGATCAC[A/G]CCACTGCACTTCAGC | 8439 |
rs113738969 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58595211 | GTAAATCCAACACTC[A/G]TGGGGTATACATCAC | 8439 |
rs113744183 | snp | C/T | 0.5 | 0 | utr-variant-5-prime, intron-variant | NSMAF | GRCh38.p7 | 8:58659354 | CCCGTCATCCAGTTC[C/T]TGTCCCCGGCAGGCT | 8439 |
rs113798347 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | NSMAF | GRCh38.p7 | 8:58609296 | TCTAGGAAATGCCTC[C/G]TAGAAGAAAGGTCTA | 8439 |
rs113829551 | snp | A/G | 0.5 | 0 | intron-variant | NSMAF | GRCh38.p7 | 8:58647314 | GATTTAATTAAACGG[A/G]CCATTTTTAAGAAGC | 8439 |
rs113847133 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | NSMAF | GRCh38.p7 | 8:58630173 | AGTTTCATGCTCACC[A/G]GGGGTGCAGGATCCT | 8439 |
rs113865246 | snp | A/C | 0.439224 | 0.163383 | intron-variant | NSMAF | GRCh38.p7 | 8:58644655 | ATTCTGCTACAAAGA[A/C]ACAGGCACACATATG | 8439 |
rs113885233 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661596 | AAAAATTACCTGGGT[A/G]CAGTGGCACACACCT | 8439 |
rs113969235 | snp | A/G | 0.0147201 | 0.0845185 | intron-variant | NSMAF | GRCh38.p7 | 8:58586035 | TCAGATATGAGTGAC[A/G]GCTTCAGAATGTGGT | 8439 |
rs113997754 | snp | C/T | 1.65534e-05 | 0.00287688 | intron-variant | NSMAF | GRCh38.p7 | 8:58601419 | TGAAATAAAATTTAA[C/T]TGGGGGTAATGATAA | 8439 |
rs114030808 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | NSMAF | GRCh38.p7 | 8:58643820 | ACAAGCATGAGCCAC[C/T]GGCCCAGCCAACAGA | 8439 |
rs114046880 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NSMAF | GRCh38.p7 | 8:58622231 | GTTGTTTAGAAAGGA[C/T]ATTTTAAAATTTATT | 8439 |
rs114068917 | snp | G/T | 0.0517044 | 0.152246 | intron-variant | NSMAF | GRCh38.p7 | 8:58647534 | CGGTAGGAGGTGATT[G/T]GATCATGGGGGTAGA | 8439 |
rs114103907 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NSMAF | GRCh38.p7 | 8:58633189 | TGGCCCACAAGGCCC[C/T]GCATGACACGGTCCC | 8439 |
rs114149618 | snp | A/G | 0.0115144 | 0.0749975 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660873 | AGCATGTATCTGTAC[A/G]GTACTTCGTTCCTTT | 8439 |
rs114194467 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | NSMAF | GRCh38.p7 | 8:58619061 | GACACATTCTAAGTA[A/G]GTCAGAAGAAGCTAA | 8439 |
rs114232060 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | NSMAF | GRCh38.p7 | 8:58614577 | AATTTGATTATCGGT[C/T]GTTGTCCTGCCTCTG | 8439 |
rs114344173 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | NSMAF | GRCh38.p7 | 8:58648260 | GCAGCAAAGGGTTTC[A/G]GAACTGGTCTGGCTG | 8439 |
rs114344372 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMAF | GRCh38.p7 | 8:58658339 | ACTAAAACCTAATCA[C/T]ATCACCAAAAACATT | 8439 |
rs114386215 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | NSMAF | GRCh38.p7 | 8:58597034 | ACAGTGACTGGGAAG[G/T]CAGACTGGACAGCTA | 8439 |
rs114418587 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58649700 | TGTTTAAAAGAGTCC[A/G]GAGCCTCCTCCTCCT | 8439 |
rs114434538 | snp | A/C/G | 0.0107246 | 0.0724382 | intron-variant | NSMAF | GRCh38.p7 | 8:58594114 | AAAGGAACTGCTCTA[A/C/G]GTTTACTTTATGTGG | 8439 |
rs114473428 | snp | G/T | 0.0298908 | 0.118541 | intron-variant | NSMAF | GRCh38.p7 | 8:58654016 | AACATTTATTTCCTC[G/T]CCCGCTGTTTTTCAT | 8439 |
rs114499353 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | NSMAF | GRCh38.p7 | 8:58623552 | GATATACCTATGGCT[A/T]CTTCCTAATATATAG | 8439 |
rs114604639 | snp | A/G | 0.0298908 | 0.118541 | intron-variant | NSMAF | GRCh38.p7 | 8:58656282 | TTGGGGATTACAGGC[A/G]TGAGCCCTGTGTCTG | 8439 |
rs114634049 | snp | A/G | 0.0333695 | 0.124785 | intron-variant | NSMAF | GRCh38.p7 | 8:58645380 | GATGAACACTAGTTT[A/G]CTGAGAATTATGGTT | 8439 |
rs114644030 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMAF | GRCh38.p7 | 8:58636736 | CAGTAAAACTTTACA[A/G]GAACAAGTGGCAGCT | 8439 |
rs114672033 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMAF | GRCh38.p7 | 8:58590202 | GCTCTCCTCCTATTT[A/G]CGCAGATTTTCTCAA | 8439 |
rs114758390 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58599684 | TCTAAGCAATAAAAT[A/G]ATTACTGAAATTGCA | 8439 |
rs114855446 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58618962 | CAGCAACTGGATACA[C/T]TAAAACGTTCACAGT | 8439 |
rs114861835 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58654787 | GATAAAACTATGACT[A/C/G]TTCCTCAGAAGGAAA | 8439 |
rs114872292 | snp | C/G/T | 0.00838764 | 0.064226 | missense, intron-variant | NSMAF | GRCh38.p7 | 8:58659270 | TCCGGGTGAGCTGCC[C/G/T]GCGGCCGCCGGGACC | 8439 |
rs115075372 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMAF | GRCh38.p7 | 8:58657314 | GAAATCTAAAATCCC[C/T]TAATTAGCATGAGAG | 8439 |
rs115146661 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58647453 | TGGACAGTGATATAG[C/T]TTGGATGTTCTGTCC | 8439 |
rs115177564 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58591184 | ACATGGTAGGTATAC[C/T]GTTGACATTTCAGCA | 8439 |
rs115290812 | snp | A/C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58623301 | ACCAGAAAAAAAGTA[A/C/T]TTATAAGTATTTATA | 8439 |
rs115400736 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58644479 | ATCAAGTGCTAGAGA[C/G]GATGTGGAGAAATAG | 8439 |
rs115502177 | snp | A/C | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58649628 | ATGCCTCAGCACCAT[A/C]CCCTTGGTAATAAGT | 8439 |
rs115503834 | snp | A/G | 0.029116 | 0.117091 | intron-variant | NSMAF | GRCh38.p7 | 8:58642708 | AAGGTTTCAAGTTAC[A/G]ATTATAACTTTTAAA | 8439 |
rs115531997 | snp | C/T | 0.0603597 | 0.1629 | intron-variant | NSMAF | GRCh38.p7 | 8:58648391 | AGCCCGGCCATGTGG[C/T]AGAGAAAGAAAAAGC | 8439 |
rs115574277 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | NSMAF | GRCh38.p7 | 8:58658988 | AGAATCAGGCCTTTC[C/T]GGCGGCCCCCCTCCC | 8439 |
rs115787885 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58634451 | TGAAGTCAGCAAGTC[C/T]GTGCATCTTTGTTCC | 8439 |
rs115888833 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58638702 | TACAGAAAAGCTTCT[C/T]GGCATTGGTCTGGGC | 8439 |
rs115890214 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | NSMAF | GRCh38.p7 | 8:58644434 | ACCAGTTCAAGTCAC[C/T]GGACTTCCAAAAAGT | 8439 |
rs115905537 | snp | A/C/T | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58597646 | AATAGGAGGGACTAA[A/C/T]CCTCAAATAATGACA | 8439 |
rs115963376 | snp | A/C | 0.0279526 | 0.114869 | downstream-variant-500B | SDCBP, NSMAF | GRCh38.p7 | 8:58583060 | CAGGGCCAAAAGAAG[A/C]GCTGGTTCACACCTG | 8439 |
rs115967796 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | NSMAF | GRCh38.p7 | 8:58630839 | TCAGATTCAGCCTGT[A/G]GGACTATGTTTGCCC | 8439 |
rs116055735 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | NSMAF | GRCh38.p7 | 8:58607415 | ATTTTGCTTTGAGAC[A/C]TAGCTGCTATGAATG | 8439 |
rs116201925 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NSMAF | GRCh38.p7 | 8:58631995 | CCACTGGTCCTTACA[C/T]AGTATATTAATAACT | 8439 |
rs116205331 | snp | A/G | 0.0193772 | 0.0965046 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661309 | ATATAAGCCCTAAGG[A/G]GCTGGAGTGATGGCT | 8439 |
rs116248212 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58617137 | GGAAGACTTTTGGGG[C/T]AGAAAAGGGTAAATT | 8439 |
rs116254184 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58639471 | GTTGTTGGCAAGAGC[A/G]TGGAGAAAAGAGAAC | 8439 |
rs116255551 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58644474 | GCAGGATCAAGTGCT[A/G]GAGACGATGTGGAGA | 8439 |
rs116358575 | snp | C/T | 0.0113802 | 0.0745694 | intron-variant | NSMAF | GRCh38.p7 | 8:58599881 | ATTAACTGAAAGTTT[C/T]GGGGAAAAATAAAAA | 8439 |
rs116544617 | snp | A/T | 0.411724 | 0.190644 | intron-variant | NSMAF | GRCh38.p7 | 8:58623302 | CCAGAAAAAAAGTAT[A/T]TATAAGTATTTATAA | 8439 |
rs116564295 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | NSMAF | GRCh38.p7 | 8:58640930 | TTTATTTATTGATTG[A/C]TTTATTTTTGAGACA | 8439 |
rs116579426 | snp | C/G | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58643435 | ACTGAACAATGCTAG[C/G]CTTCCCCACCTCTTC | 8439 |
rs116612002 | snp | C/T | 0.0341408 | 0.126114 | intron-variant | NSMAF | GRCh38.p7 | 8:58658572 | TGTAACCTGCTTTGC[C/T]GGTATTCACTGATGA | 8439 |
rs116638259 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | NSMAF | GRCh38.p7 | 8:58625930 | TAAAATTTATTTTGA[C/T]AGTTTTTGTGGTACA | 8439 |
rs116639554 | snp | A/T | 0.0325976 | 0.123435 | intron-variant | NSMAF | GRCh38.p7 | 8:58632819 | TTAAATCTCACATCC[A/T]ACTTGAAGCCTGCTC | 8439 |
rs116670146 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58647556 | GGGGGTAGATCCCTC[A/G]TGACTCAGCACCATC | 8439 |
rs116673198 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58644670 | AACAGGCACACATAT[A/G]TTTAATGCGGCACTG | 8439 |
rs116987489 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58639918 | ACTACATGATTTCAC[A/G]TAGACTCTAAAAGAG | 8439 |
rs117063745 | snp | C/G | 0.0314385 | 0.121371 | intron-variant | NSMAF | GRCh38.p7 | 8:58602804 | TTAATTTTCTTCTTT[C/G]ATTATTTCAGGACTT | 8439 |
rs117087142 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58627092 | TGTTTGAGGTTCCTC[A/G]TAGATTCTGGATGTT | 8439 |
rs117164295 | snp | C/T | 0.118235 | 0.212457 | intron-variant | NSMAF | GRCh38.p7 | 8:58639278 | GACAGAGTGAGACTC[C/T]GTCTCAATAAAAAAA | 8439 |
rs117167909 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58652324 | CTGCAAAGTTTCAGG[C/G]AAAACTGCTATGATT | 8439 |
rs117187681 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | NSMAF | GRCh38.p7 | 8:58643767 | AACTCCCAACCTCAC[A/G]TAATCCACCCACCTC | 8439 |
rs117413256 | snp | C/T | 0.0048914 | 0.0492115 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58595652 | CAGGTCTTCAAAAGA[C/T]TCTTCACCTGGAGAG | 8439 |
rs117475935 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | NSMAF | GRCh38.p7 | 8:58649350 | TTTTGATTTTACAGG[C/T]TCATAGGTGGAAAGA | 8439 |
rs117607963 | snp | A/C | 0.40853 | 0.193309 | intron-variant | NSMAF | GRCh38.p7 | 8:58592919 | AAAACAACAACAACA[A/C]AAAAAAAACCTCTCT | 8439 |
rs117703176 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | NSMAF | GRCh38.p7 | 8:58626866 | CAAATCCATGCCAAC[A/G]TCTATTATTTTTTGA | 8439 |
rs117884048 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | NSMAF | GRCh38.p7 | 8:58633812 | TGCCTGGTTGTATAC[C/T]TGACACAGGAAGCTT | 8439 |
rs118011811 | snp | C/T | 0.0535932 | 0.154675 | intron-variant | NSMAF | GRCh38.p7 | 8:58646840 | AGACTCTTAGCCCTG[C/T]CCCTACATATTCCTA | 8439 |
rs118039071 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58609151 | GCTCATAGTGCTCCT[A/T]CAGGAAAAATTCAGA | 8439 |
rs118060071 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58645315 | TATCAGGCACAGTGG[A/G]GAGCAGGATTGTAGT | 8439 |
rs118128651 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58644086 | TTGTGATAAGGACCA[A/G]GAAACATCAATGAGT | 8439 |
rs137894141 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58644936 | ATGGACACAGGGAGG[C/T]GAACATCACACACGG | 8439 |
rs137945277 | in-del | -/TCTT | 0.371987 | 0.218218 | intron-variant | NSMAF | GRCh38.p7 | 8:58629410 | TCTTTGTTAATATTC[-/TCTT]TGTTAAAATTCTCAT | 8439 |
rs137997625 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58652526 | TGAGCTGGGATGAGT[A/G]AGCCAAGGTTCCATC | 8439 |
rs138006293 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58624893 | TTCTCCCTTCAGTTC[C/T]ATCAATGTTCGCTTC | 8439 |
rs138041844 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58605621 | AGACCCACAAAGAGG[C/T]GATTCTACAAATAGC | 8439 |
rs138116298 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58594549 | GCTTTACATATTCCT[A/G]ACAATTTCTGGCAAT | 8439 |
rs138220588 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58646670 | ATGTAAAAATTATTA[C/T]AATTAAGTTGCATGA | 8439 |
rs138228792 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58639198 | CTAAGGCAGGAGAAT[C/T]GCTTGAACCCGGAAG | 8439 |
rs138347708 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58634367 | AGTGCTGGGAGCATG[C/T]TCTTCCCCTCCCCAT | 8439 |
rs138352251 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58631299 | AGGCACTTTTTTTTT[-/T]AAGTCAAAAAGTTAA | 8439 |
rs138354390 | snp | A/G | 0.00279162 | 0.0372561 | downstream-variant-500B | SDCBP, NSMAF | GRCh38.p7 | 8:58583331 | TATACAGCTTACCTT[A/G]TTTGAAATTTAGAAG | 8439 |
rs138393448 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58647501 | GAAATGTGATTCCCA[A/G]CGTTGAAGGTGGAGG | 8439 |
rs138445971 | in-del | -/TG | 0.172997 | 0.237846 | intron-variant | NSMAF | GRCh38.p7 | 8:58603725 | TCCCTCCAAATGTGC[-/TG]TGTCTCCATGCATTT | 8439 |
rs138504485 | snp | A/G | 8.24273e-05 | 0.00641926 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58609619 | CGGGTAGCCGTTGAG[A/G]GGCTGAAAATACAGG | 8439 |
rs138530641 | snp | A/G | 8.23811e-05 | 0.00641746 | missense | NSMAF | GRCh38.p7 | 8:58586523 | TGCATTAAGGTGGCC[A/G]TTGTGAGGTCCCAAA | 8439 |
rs138534625 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58620486 | CTTTATCCTGAAGGC[A/T]CTGGGGATGGGGGCG | 8439 |
rs138554941 | snp | A/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58586156 | CTCTCCTTGAAATGG[A/T]TCTAGCCCTTTCCAA | 8439 |
rs138561357 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58600160 | GTTCTAACCATCTCT[C/G]TGAGTGTCCCACTTT | 8439 |
rs138598489 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58627783 | TTGTGAAAATGACCA[C/T]ACTGCCTAAAGCAAG | 8439 |
rs138599020 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | NSMAF | GRCh38.p7 | 8:58644677 | ACACATATGTTTAAT[A/G]CGGCACTGTTCACAA | 8439 |
rs138612248 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | NSMAF | GRCh38.p7 | 8:58607688 | ACTTTCAGACATCCC[A/G]TAAGTGTTTACCGTC | 8439 |
rs138626790 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58615520 | AATTATAAATCAGTA[C/T]CTATAAAATATCTAC | 8439 |
rs138678600 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58633985 | AAATAACTAAAATGT[A/T]TAGTTTTATAATGAA | 8439 |
rs138858711 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58599563 | TCACATTAAGGTCTC[C/T]CAAATATATATTAAT | 8439 |
rs138913786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58595935 | TCTAACTTATGAATT[C/T]GGGGAAATACAAGAC | 8439 |
rs138913829 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58643269 | CTTGCCTTGTGTCCA[A/T]ATAACTACTATGTCA | 8439 |
rs138928312 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58655236 | CTTGGCCTCCCAAAG[G/T]GCTGGGATTACAAGT | 8439 |
rs138959726 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | NSMAF | GRCh38.p7 | 8:58621148 | TGTTCCCTTCTTTGC[A/G]TCCATTTGTACTCAA | 8439 |
rs138976513 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58610983 | TGACAGATTTGATTG[A/T]CAGAGCCTCCCTGTA | 8439 |
rs139025201 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | NSMAF | GRCh38.p7 | 8:58657936 | TACATGGAAATGCAA[C/G]TACAGGTTTCAAGGT | 8439 |
rs139107276 | in-del | -/AAC | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58629623 | TATCCACACATTAAA[-/AAC]AACAACAACAACAAC | 8439 |
rs139257218 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58649745 | CTCTTGCCATGTGAT[A/G]TACCTGCTCCCACTT | 8439 |
rs139260915 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | NSMAF | GRCh38.p7 | 8:58591788 | AACTGTGCCCGGCCT[C/T]AAAACAACCTCTTAA | 8439 |
rs139321192 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58587472 | AACCTAAAGAGTCAA[C/G]ACAAAGAAAAGAACT | 8439 |
rs139325712 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58588136 | GGAATTCTAACAATT[C/T]TAGGTTCTTGCTTTC | 8439 |
rs139327692 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | NSMAF | GRCh38.p7 | 8:58636085 | ATCATTTTTCCAAGT[C/T]GTTAACTGCATTTAC | 8439 |
rs139353415 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58602831 | ACTTTCCAAGTGTTC[C/T]ATAACAAATAATCAC | 8439 |
rs139355331 | snp | A/G | 0.000181233 | 0.00951753 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58599778 | GGGAAGCTCCACGTC[A/G]TCAACCATCTGTCCT | 8439 |
rs139360502 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58645697 | GGCTACAATTAATAT[C/G]CCTACAAAGAAGAAG | 8439 |
rs139378838 | snp | G/T | 0.00953873 | 0.0683987 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661541 | TCGAGACCAGCCTGG[G/T]CAACAAAGCAAGACC | 8439 |
rs139397159 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMAF | GRCh38.p7 | 8:58589908 | TTAGAAAACAGTGCT[A/G]TGTCCTGGCAGGGAA | 8439 |
rs139446771 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58631031 | TATGCTTAAGTGAAA[A/G]GTCCCAGGGAACCAG | 8439 |
rs139458676 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58636945 | AATGCTTGATTCTTT[A/G]CCTTTATTTATCAAG | 8439 |
rs139539085 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58645459 | TTGGAAAAAACTAAA[-/C]CAGCCTCAGAGAAAA | 8439 |
rs139562997 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58629558 | TATTTTGTACCTCTG[A/G]TTGGACTATTTTTCT | 8439 |
rs139596316 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58637102 | TTAACATTTATGAAA[C/T]ATTTCAATCCATTGC | 8439 |
rs139692322 | snp | G/T | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58612963 | CTGTCAACCTAGAAT[G/T]CTATATCCAAAAACA | 8439 |
rs139716198 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58616874 | AATGAGTGAATTTAG[A/G]AGAGTCATAGTATAC | 8439 |
rs139776887 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58612363 | TCTATGTGCCAGGAG[A/G/T]GTGATGTACCCTCAC | 8439 |
rs139778478 | in-del | -/A | 0.0260105 | 0.111035 | intron-variant | NSMAF | GRCh38.p7 | 8:58607918 | AGTATCAGAAAGGGG[-/A]AAAAAAAATCACCAA | 8439 |
rs139786186 | snp | A/G | 8.26849e-05 | 0.00642928 | missense | NSMAF | GRCh38.p7 | 8:58623251 | ATGTTCTAGCTAAAC[A/G]AGACTGCAAAATAGC | 8439 |
rs139813149 | snp | C/G | 0.0283406 | 0.115616 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660030 | GCATAAAAAGGGATG[C/G]TGGCCCATAAACCAC | 8439 |
rs139863054 | snp | C/T | 0.000165082 | 0.0090837 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58635307 | GAAAATGACATACTT[C/T]GTGAAGTGTCTATTG | 8439 |
rs139896943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58622542 | AGGATTACAGGTGCC[C/T]GCCACCATGCCTGGG | 8439 |
rs139986925 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58592536 | CAGTAATATGAATTA[C/T]GAAAATCTAAATATG | 8439 |
rs140016602 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | NSMAF | GRCh38.p7 | 8:58658632 | GATCTGTGGCTCTCA[C/T]AATCAAAACAGTGTG | 8439 |
rs140016690 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58618008 | GAGTTCATGTCCTTT[G/T]CAGGGACATGGACGA | 8439 |
rs140109769 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58611825 | TAACTTAAGTATAAC[C/T]GATTATAAAAGAAAA | 8439 |
rs140141320 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58608753 | TGAGCCCCACCACCT[A/G]GTGGACACAATCACT | 8439 |
rs140144207 | snp | A/G | 4.95503e-05 | 0.00497722 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58589488 | TGCAGAATATAGCCT[A/G]TTGTCATGCCAACAG | 8439 |
rs140163032 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660551 | TTGGGATATAACTCA[C/T]ATACCAAACAAGTCA | 8439 |
rs140199734 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | NSMAF | GRCh38.p7 | 8:58649079 | TGAAAGCAGCCAAGT[A/G]GGCTGCACCCTTCAA | 8439 |
rs140230826 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58589374 | CTTATAATATCTGTA[C/T]GTACATTTTAAGCTA | 8439 |
rs140238260 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58624873 | ATTATTGTGTTGCTA[G/T]CTATTTCTCCCTTCA | 8439 |
rs140271902 | snp | A/C/T | 0.0138799 | 0.0821421 | intron-variant | NSMAF | GRCh38.p7 | 8:58605139 | AATGTAATAAAAAAA[A/C/T]TTTGGGCTTGAACAT | 8439 |
rs140279762 | snp | A/G | 6.58946e-05 | 0.0057396 | missense | NSMAF | GRCh38.p7 | 8:58603282 | GGTCGTTGCAGCTGC[A/G]GTCGGCCAGGTTGTT | 8439 |
rs140301116 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58619184 | TGGAAATAAAATTAA[C/T]GCTATATAGTGAAGC | 8439 |
rs140329740 | in-del | -/AT | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58641471 | CCGATTTTTAAAAAC[-/AT]AGTGATAAATCTGCC | 8439 |
rs140337580 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58646149 | TAATCTGTAACTTTT[A/G]TTGACCTGTCCTCCA | 8439 |
rs140433357 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58597691 | GGATTGTCTAAACCT[A/C]ATTATAGACCTTCAG | 8439 |
rs140433686 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58639152 | TAGCCAGAAATGGTG[G/T]CACGTGCTGTACGCC | 8439 |
rs140438385 | snp | C/T | 0.00110309 | 0.0234591 | missense | NSMAF | GRCh38.p7 | 8:58585736 | GACTGCCAGATAAAA[C/T]GGAATTTCCATCCCA | 8439 |
rs140503497 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58656281 | TTTGGGGATTACAGG[C/T]GTGAGCCCTGTGTCT | 8439 |
rs140579437 | snp | C/G | 0.00268797 | 0.0365617 | missense | NSMAF | GRCh38.p7 | 8:58599762 | CACTGGAAGCCCAAG[C/G]GGGAAGCTCCACGTC | 8439 |
rs140586276 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58593806 | CTAAATCAAATATCC[C/T]GAAGAAATATACACT | 8439 |
rs140614316 | in-del | -/A | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58647595 | GATAAATGAGTTCAC[-/A]ATCTGTTCACTCAAG | 8439 |
rs140695181 | in-del | -/TG | | | intron-variant | NSMAF | GRCh38.p7 | 8:58624174 | AGCCTCCCGAGTAGC[-/TG]GGGCTAGAGGTGTGC | 8439 |
rs140730866 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58583597 | AACTTACTAAGAACT[A/G]CTAATCCTTCTCCAG | 8439 |
rs140758394 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58627091 | TTGTTTGAGGTTCCT[C/T]GTAGATTCTGGATGT | 8439 |
rs140792558 | snp | C/T | 0.0475351 | 0.146656 | intron-variant | NSMAF | GRCh38.p7 | 8:58588755 | CATTGTTCCTTCTTT[C/T]CTTTGTCATCTTGGA | 8439 |
rs140817904 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58644111 | ATGAGTTACAGGCAA[A/C]AGCTTTCATGAAAAG | 8439 |
rs140848286 | in-del | -/ATC | | | intron-variant | NSMAF | GRCh38.p7 | 8:58646044 | AGACTCCGTCTCAAA[-/ATC]ATCATCATCATCATC | 8439 |
rs140849154 | in-del | -/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58626287 | TTTTAGTAGAGACAG[-/C]GTTTCACAGTGTTAA | 8439 |
rs140903039 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | NSMAF | GRCh38.p7 | 8:58624299 | TGATCCACCCGCCTC[A/G]GCCTCCCACAGTGCT | 8439 |
rs140916412 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58641835 | ACACCTACATGGGGC[C/T]GTACCATTTTGCCCT | 8439 |
rs140928325 | snp | C/T | 3.33072e-05 | 0.00408075 | missense | NSMAF | GRCh38.p7 | 8:58590032 | CCCATGAAGAAGTTA[C/T]GACAGTGGCATCTCC | 8439 |
rs141143369 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58640671 | AAAATAATTTTCTGT[A/G]GCTAACTCCAACTTT | 8439 |
rs141171976 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58651763 | GTTATCTAGCGCAGC[A/G]CTTCACAAAGGTTAG | 8439 |
rs141212033 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58645488 | AAAGCCAGGTCTCTA[C/T]AACATCATCCCACAG | 8439 |
rs141228279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58642665 | TCTACAACCCCAGAA[C/T]TGGAACAAATGCTTT | 8439 |
rs141283122 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58639227 | AGGCAGAGGTTGCAG[C/T]GAGCAGAGATCACGC | 8439 |
rs141322725 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58597128 | GAAAGAGAACCACAT[C/G]AAAACATATATGGCC | 8439 |
rs141379793 | in-del | -/A | 0.0402882 | 0.136092 | intron-variant | NSMAF | GRCh38.p7 | 8:58652160 | GCAGGATAGATGAAG[-/A]AAAAAAAAATCTATA | 8439 |
rs141403706 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | NSMAF | GRCh38.p7 | 8:58614106 | TCCTCACAATGACCA[C/T]TGCCTAACAACACGT | 8439 |
rs141442542 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | NSMAF | GRCh38.p7 | 8:58628200 | GTAGAAGAATGAAAC[C/T]GGATCCTTATCTCTT | 8439 |
rs141561489 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58625277 | GTCTGGAATTCTTGG[C/T]CTCTATAATCACATG | 8439 |
rs141635262 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | NSMAF | GRCh38.p7 | 8:58614653 | CCCCTTTGGAGAAGT[A/G]TGTATAAAAGTCAAG | 8439 |
rs141749982 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58632164 | ACACCTCCCCAAACC[C/T]GTCAGATATTCAAAA | 8439 |
rs141760460 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58627584 | CCAAGCTAAGAATCA[A/C]ATCAACAATTCCATT | 8439 |
rs141793921 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58630088 | AATTTCTTCCCAATC[A/G]TGTGGTGCTGTGTGG | 8439 |
rs141877327 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | NSMAF | GRCh38.p7 | 8:58591628 | AATAGCTGGGATTTT[C/T]TGACGTGCACACCAC | 8439 |
rs141916240 | in-del | -/AGAGT | 0.0715223 | 0.175059 | intron-variant | NSMAF | GRCh38.p7 | 8:58653131 | ACACTGGTAGAGAGG[-/AGAGT]AAAGATAATGATTAG | 8439 |
rs141959844 | snp | G/T | 0.000153988 | 0.00877328 | stop-gained | NSMAF | GRCh38.p7 | 8:58609697 | CACCATTTCTGCTTT[G/T]CATTCCATGTGCAGC | 8439 |
rs141973474 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58657888 | AGCCTATCACGTTGT[C/T]GTCTAATCAATGAAT | 8439 |
rs142087727 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58588915 | GACCATTCATCCCAC[A/G]ATGGAATACACAGTA | 8439 |
rs142092969 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58631999 | TGGTCCTTACATAGT[A/G]TATTAATAACTATGT | 8439 |
rs142123842 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58616582 | CTCTCAGTAAACTAG[G/T]AACAGAAAGGAATAT | 8439 |
rs142165848 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58613475 | ACACAAAGTGCTACA[A/G]CTAAAAAGTCAATAG | 8439 |
rs142178018 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58654433 | CGCATGCCTGTAATC[C/T]CAGCTACTTGGGAGG | 8439 |
rs142178137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58610784 | GTGCAAAACAAGGGA[A/C]ATCTCCCACAGTTCA | 8439 |
rs142189452 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58611871 | AGAGGAAATGGAGAA[A/G]AGAATGGCTGAGAAC | 8439 |
rs142189658 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58655252 | GCTGGGATTACAAGT[A/G]TAAGCCATGGCACCT | 8439 |
rs142191042 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMAF | GRCh38.p7 | 8:58585266 | GAGGTAGGAGTCAGC[A/G]GTAGAAAGAAGCCTT | 8439 |
rs142203067 | snp | A/T | 0.0146672 | 0.084371 | intron-variant | NSMAF | GRCh38.p7 | 8:58653831 | AAAATTTTTAATGAA[A/T]ATTATATAGCTTACA | 8439 |
rs142243518 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58651537 | ATCCATAAAGCCAGT[A/C]AATTCTATTTTCAAG | 8439 |
rs142278918 | snp | C/T | 0.000247168 | 0.0111141 | missense | NSMAF | GRCh38.p7 | 8:58602120 | TGAGATCCCGGAAGG[C/T]TCCTGGATTTGACAA | 8439 |
rs142293482 | snp | A/G | 0.000313203 | 0.0125101 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58609655 | GTCCGTGATGCACAC[A/G]TGTCCAGGATTAGTC | 8439 |
rs142450621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58638961 | TATTAAAAGACAGGC[A/G]GAGGACCTGAATAGA | 8439 |
rs142454070 | in-del | -/TATA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58604565 | ATATATAATATATAT[-/TATA]ATATAAACCTACTTT | 8439 |
rs142532753 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58593362 | GCTACAGATCATAAA[C/T]AATGATAACAGAATC | 8439 |
rs142537914 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMAF | GRCh38.p7 | 8:58596404 | CTCCACAGAGTGTCA[A/G]CCTCCTTCTGGAAGC | 8439 |
rs142542935 | snp | A/G | 0.000494454 | 0.0157157 | missense | NSMAF | GRCh38.p7 | 8:58589537 | TCATGTCCCATTAAC[A/G]TGTCCTGGCGTCTTC | 8439 |
rs142545036 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58638828 | AATTAACAAAGTCAA[A/G]AGACAACCTACGGAA | 8439 |
rs142605608 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58592250 | TCTCTCCTTGATGTC[C/T]AGTGGTTAGGATTTG | 8439 |
rs142618981 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58636209 | ATGGCCTAGCTCTAC[A/G]ATTGTCAATATGTGG | 8439 |
rs142642956 | snp | A/G | 0.000400982 | 0.0141538 | intron-variant | NSMAF | GRCh38.p7 | 8:58623805 | AGGGGAAGATATCAA[A/G]ATACAGGAAGAGAAG | 8439 |
rs142652236 | snp | G/T | 0.12932 | 0.218944 | upstream-variant-2KB, utr-variant-5-prime | NSMAF | GRCh38.p7 | 8:58659781 | GCGGCGCCGCTGGGC[G/T]GCCGAGAGCCCGACG | 8439 |
rs142686417 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMAF | GRCh38.p7 | 8:58611031 | TAAGAGGTGGCTTGA[C/T]CACTTCTGGAGGTAA | 8439 |
rs142821507 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58653956 | AGGCTAGTAATACAT[C/T]TTGGGTAAAGTCAAT | 8439 |
rs142844478 | snp | A/C/T | 8.40394e-05 | 0.00648181 | missense | NSMAF | GRCh38.p7 | 8:58590008 | GCACAGATACATACA[A/C/T]ATTATTATCCCATGA | 8439 |
rs142915707 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58608370 | GAAGAAAATTGTCTT[G/T]CTTTTCTATAATTTT | 8439 |
rs142942697 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | NSMAF | GRCh38.p7 | 8:58653106 | AGCAGTTAAGTGTTC[C/T]AAGGTTCTTACACTG | 8439 |
rs142982194 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58612386 | ACCCTCACTCCACAG[C/G]GACAGAAGCTCCTGC | 8439 |
rs143006088 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58648374 | AACTCTGGGAAATTT[A/G]TAGCCCGGCCATGTG | 8439 |
rs143043635 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | NSMAF | GRCh38.p7 | 8:58587204 | CTTGACCATCCCAGA[C/G]AGCTGGTCACTGTCC | 8439 |
rs143050199 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMAF | GRCh38.p7 | 8:58657937 | ACATGGAAATGCAAG[C/T]ACAGGTTTCAAGGTT | 8439 |
rs143061129 | snp | A/G | 0.000148425 | 0.0086134 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58623745 | ATCTTCCACTTTCCC[A/G]GGAACATCCAATTCA | 8439 |
rs143061385 | in-del | -/TTTTCT | 0.0596104 | 0.162024 | intron-variant | NSMAF | GRCh38.p7 | 8:58650443 | TATTTGCTAGCCTGA[-/TTTTCT]TTTTCTTTTTTAGCT | 8439 |
rs143063886 | in-del | -/TTG | 0.079617 | 0.182947 | intron-variant | NSMAF | GRCh38.p7 | 8:58595114 | TTAGAAGCATAATTA[-/TTG]TTTTTAAAATTCATG | 8439 |
rs143199390 | snp | C/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660261 | GAAATTCTGGCTGAA[C/G]CAACCTAACAGGAGT | 8439 |
rs143256721 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMAF | GRCh38.p7 | 8:58628065 | GGAACAGAACAGACA[A/G]CCCAGAAATAAAGCC | 8439 |
rs143359529 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | NSMAF | GRCh38.p7 | 8:58625088 | GAGTAAAACAGATTG[A/C]CCTCCCCAATGTGGG | 8439 |
rs143400607 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58646719 | TCAAACTACATTTTA[A/C/T]GGAGTAAAAGAGTCC | 8439 |
rs143437399 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | NSMAF | GRCh38.p7 | 8:58626116 | TTTTTTTTTTTTGAG[A/C]TGGAGTCTCACTGTG | 8439 |
rs143464405 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58654794 | CTATGACTCTTCCTC[A/T]GAAGGAAACATATCT | 8439 |
rs143464800 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58644979 | GGGGTGGGGAGCTAG[A/G]GGAGGGATAGCATTA | 8439 |
rs143492573 | snp | C/T | 0.000148249 | 0.00860829 | missense | NSMAF | GRCh38.p7 | 8:58597458 | TTTGGGGTGATCCTT[C/T]GAGGATGTGGTGTCA | 8439 |
rs143505109 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58624423 | AACTTCCCTGTTTAT[A/G]CTGCTTTTGCTGCAT | 8439 |
rs143612297 | in-del | -/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58656024 | CCTGCTATCTAAATC[-/T]TTTTTTTGTTTGTTT | 8439 |
rs143614595 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58614154 | GCGGGAAATTAAAGA[A/C]AAATAAAATTAAAAA | 8439 |
rs143673373 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58590808 | GTATTATTGTATGGG[C/T]GTGTATAAAACAAAC | 8439 |
rs143700391 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58606391 | TTCTTCAAACATAAA[C/T]GTCTAGCTTTCTTTC | 8439 |
rs143706617 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58634124 | CAGAATTATTAATAA[C/T]GATGTTTGGTCCCCA | 8439 |
rs143723291 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58646016 | ACTGCACTCCAGCCT[A/G]GGCAACAAGAGCGAG | 8439 |
rs143744312 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58657768 | ATATAAAACACATGG[A/C/T]GCCAACTTTTTCAGA | 8439 |
rs143780760 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58586215 | ATGAGTTCATTTTTA[C/T]CTTAAATTAATTTCT | 8439 |
rs143795707 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | NSMAF | GRCh38.p7 | 8:58598570 | CATAGGAATTGAGGC[C/T]ACTGTTCTATCACAC | 8439 |
rs143811464 | snp | A/G | 0.000511378 | 0.0159821 | missense | NSMAF | GRCh38.p7 | 8:58609680 | TTAGTCACCAGAGGC[A/G]TCACCATTTCTGCTT | 8439 |
rs143812039 | snp | C/G | 0.00199481 | 0.0315187 | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58583565 | TAATGAAATACAAAC[C/G]GTTCCTATACACAGT | 8439 |
rs143815884 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58627975 | GCATCACATTATTCA[A/G]CTTCAAAATATACTA | 8439 |
rs143817244 | snp | A/G | 9.90737e-05 | 0.00703754 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58589491 | AGAATATAGCCTGTT[A/G]TCATGCCAACAGATC | 8439 |
rs143857347 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58608923 | GTTAGGATTTCTGTT[C/G]TTTTAATGGATCATG | 8439 |
rs143879961 | snp | A/C/T | 0.0142982 | 0.0835538 | intron-variant | NSMAF | GRCh38.p7 | 8:58625519 | TTTCTGATAAATTGA[A/C/T]CCTTTTATCATTACA | 8439 |
rs143916762 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58603650 | TAAACAAATACAAAA[A/G]TGTAGCGCAAATATA | 8439 |
rs143955175 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | NSMAF | GRCh38.p7 | 8:58611565 | TGAAAAGACAGAGTT[C/T]CAGCAGAGAAATAGA | 8439 |
rs143992092 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58648543 | AAGTCATTTCAGAAG[-/T]TTTTCAGGATGTCCC | 8439 |
rs144003915 | snp | A/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58626600 | TATAGGACTTTTTCC[A/T]CTTGTTGGTTGATGG | 8439 |
rs144005823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58625706 | TTGCAGATGGCATAT[A/G]GTTTTAGATCTTATT | 8439 |
rs144059643 | snp | A/G | 6.59326e-05 | 0.00574125 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58586564 | GCCTTCTTTGGTGCC[A/G]GAAACTAACAGTGTG | 8439 |
rs144123853 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58588160 | TGCTTTCTTTTACAC[C/T]AACACAAAATAGAAA | 8439 |
rs144140694 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58639810 | TGGAATATTATTCAG[C/T]CTCAAAAAAGGAAAT | 8439 |
rs144156948 | snp | C/T | 0.000642605 | 0.0179134 | intron-variant | NSMAF | GRCh38.p7 | 8:58585874 | CTGTAAATGTCTTCG[C/T]CCCCAGTAACTCACA | 8439 |
rs144157766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58631106 | ACTTACAAATTATTA[C/T]TGAGTTCTCAAATAA | 8439 |
rs144205198 | in-del | -/TAA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58591941 | CTGCACAGTATAACT[-/TAA]TAATTCAACCCAATT | 8439 |
rs144218057 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | NSMAF | GRCh38.p7 | 8:58655885 | GCACTCCAGCCTGGG[C/T]GAGAGTGAGACTCCG | 8439 |
rs144256965 | snp | G/T | 0.000611151 | 0.01747 | missense | NSMAF | GRCh38.p7 | 8:58601306 | AACATTCTATCTGCA[G/T]TATCAAATCTTCCAT | 8439 |
rs144276701 | snp | A/T | 4.94531e-05 | 0.00497234 | missense | NSMAF | GRCh38.p7 | 8:58599859 | ATCATCACCATAGAA[A/T]TCTGGAATTAACTGA | 8439 |
rs144319758 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NSMAF | GRCh38.p7 | 8:58597701 | AACCTCATTATAGAC[A/C]TTCAGAATATTTTCT | 8439 |
rs144463073 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58645766 | AAATAATAGGCCAGG[C/T]GCAGCGGCTCACACC | 8439 |
rs144515120 | snp | A/G | 0.000214127 | 0.0103449 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58603271 | GTACTGGGAGAGGTC[A/G]TTGCAGCTGCGGTCG | 8439 |
rs144527895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58587777 | TGCATTCAAGAAAAA[C/T]TCCTATGCTCAATTT | 8439 |
rs144534227 | snp | C/T | 0.00582728 | 0.0536627 | upstream-variant-2KB, intron-variant | NSMAF | GRCh38.p7 | 8:58659427 | TTTCCGCCACAGCCC[C/T]CAGCCCAGGCCCTGG | 8439 |
rs144552140 | snp | G/T | 0.000153988 | 0.00877328 | missense | NSMAF | GRCh38.p7 | 8:58643017 | TTGTGCAAAATGTGA[G/T]TGGCTCTATGCTGTT | 8439 |
rs144600575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58600336 | ACACTGAAAGATTAG[C/T]ACCACTGGTAGGGCG | 8439 |
rs144608080 | snp | A/G | 0.00412994 | 0.0452539 | missense | NSMAF | GRCh38.p7 | 8:58607807 | TTTTGTAGATGCGGC[A/G]GACATCTTGGAGTGT | 8439 |
rs144620540 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | NSMAF | GRCh38.p7 | 8:58620461 | TTGGGGCCATGTTAA[A/G]GTGTTTAGGCTTTAT | 8439 |
rs144634636 | snp | C/T | 0.00028131 | 0.0118565 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58601449 | AAGAATCTTACCAAT[C/T]CTAACAAGATAAAAA | 8439 |
rs144667907 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58657569 | ATTCCTCTGTTTCAG[A/G]ATGAATTCTAAGATT | 8439 |
rs144678337 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | NSMAF | GRCh38.p7 | 8:58656007 | CAATATGGTTCCTGC[C/T]ATCTAAATCTTTTTT | 8439 |
rs144679672 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58655154 | TATTTATTTTTTAAA[C/T]AGAGAAAAGGTCTCC | 8439 |
rs144693853 | snp | A/G | | | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58583907 | TTTCCTAACACAGCC[A/G]CATTTTATCTGCCCT | 8439 |
rs144708345 | in-del | -/AAATAATAAAAT | 0.216472 | 0.247742 | intron-variant | NSMAF | GRCh38.p7 | 8:58606052 | ATAAATTCAAAAAGA[-/AAATAATAAAAT]AAATAATAAAATAAA | 8439 |
rs144737228 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58585043 | GGGATAACAAGAGAC[A/T]CTAGAAGAATTAAAA | 8439 |
rs144741992 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58654255 | CTTGCCAAGTGCTTT[G/T]TATAAAATAAATATA | 8439 |
rs144846583 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58653850 | ATATAGCTTACATAC[A/T]CAAAATCCATTTATG | 8439 |
rs144877578 | snp | C/T | 9.30501e-05 | 0.00682029 | missense | NSMAF | GRCh38.p7 | 8:58631527 | GGTGCAACAACATTA[C/T]GTTCTTTAATGAAAT | 8439 |
rs145049734 | snp | C/G/T | 0.0180909 | 0.0933734 | intron-variant | NSMAF | GRCh38.p7 | 8:58643086 | AATCTGGATTTGGGG[C/G/T]GAAAAAACAACTTTC | 8439 |
rs145050534 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58595781 | CACCCTGTCACAATA[C/T]AACTGCTTTGAAATG | 8439 |
rs145137115 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58620022 | AGATACAGACGAATC[A/G]CCTAAATCTCCTTGA | 8439 |
rs145150387 | snp | A/C | 0.00055788 | 0.0166922 | intron-variant | NSMAF | GRCh38.p7 | 8:58637373 | TGGTGCTGATTGCAA[A/C]TGAGTTATTTCTAGG | 8439 |
rs145238522 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58610241 | TCTGTGAATTTACTG[C/T]AGAAAACCTCTGAAA | 8439 |
rs145287691 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58649946 | GTGGTTTATAAATAA[C/T]CTGTCTGATCTAGAA | 8439 |
rs145302601 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661024 | TTTTTATGGACCTAT[A/G]TTTCCATTTCTGTTG | 8439 |
rs145313280 | snp | A/G | 0.000307953 | 0.0124049 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58590071 | GTAAACAAGACGATA[A/G]AGCCTGAAATACAAA | 8439 |
rs145334211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58624892 | TTTCTCCCTTCAGTT[A/C]TATCAATGTTCGCTT | 8439 |
rs145346621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58620608 | GTGTATGGCTGTAAA[A/G]GACTATTTGTGTCTT | 8439 |
rs145400140 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58623563 | GGCTTCTTCCTAATA[C/T]ATAGTTTTTAAACTC | 8439 |
rs145443754 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58592763 | ACGATGGTGGGTGCC[C/T]GTGAACCCAGCTACT | 8439 |
rs145506455 | in-del | -/TATATATGTATGTATGTATG/TATATATGTATGTATGTATGTATG | 0.278399 | 0.248382 | intron-variant | NSMAF | GRCh38.p7 | 8:58625394 | ATATATGTATATGCA[lengthTooLong]TATGTATGTATGTAT | 8439 |
rs145605691 | snp | C/G | 1.64749e-05 | 0.00287005 | missense | NSMAF | GRCh38.p7 | 8:58643023 | AAAATGTGATTGGCT[C/G]TATGCTGTTCAAAGT | 8439 |
rs145670976 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58604009 | ATCTTAGATAAATGC[A/G]GCAATGAGAACTTCC | 8439 |
rs145717567 | snp | A/T | 0.0134861 | 0.0810011 | intron-variant | NSMAF | GRCh38.p7 | 8:58600085 | TAGCAGCATTTCCTA[A/T]GCACTTGGGGGCTGT | 8439 |
rs145730575 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58646720 | CAAACTACATTTTAC[A/G]GAGTAAAAGAGTCCA | 8439 |
rs145789659 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58627367 | AAGTCCTAGCCACAG[C/T]AATCAGACAGAAAAG | 8439 |
rs145857425 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58641849 | CTGTACCATTTTGCC[C/T]TAATAGTTACTTTAA | 8439 |
rs145930714 | snp | A/G | 1.65425e-05 | 0.00287593 | stop-gained | NSMAF | GRCh38.p7 | 8:58597546 | TCTCATCAGGATCCT[A/G]GATGCTTTGGGACAG | 8439 |
rs146010335 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | NSMAF | GRCh38.p7 | 8:58596564 | GCCCAGCGCAGAACA[C/G]ATACCCTGTAAATGT | 8439 |
rs146013099 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMAF | GRCh38.p7 | 8:58613837 | ATATCGGTGTGCCTC[C/T]CTAATCACAAAATCT | 8439 |
rs146029974 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58592278 | TTGGTGCTCTCACTG[A/C]AGCAGCCTGGGTTCA | 8439 |
rs146075702 | in-del | -/TA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58606215 | ACATATACGTTTGCG[-/TA]TATATATATATGTTG | 8439 |
rs146112363 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | NSMAF | GRCh38.p7 | 8:58653286 | TCCAAAGGAAGAAGG[G/T]AAGGAAGGCAAAATA | 8439 |
rs146130275 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58610872 | GAGATCCCAAGTCCT[A/G]TGGAAGAGAAAGTCT | 8439 |
rs146147055 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58648793 | AGAATGCAAGCATGA[A/G]GGAGCCTTGGCAGCT | 8439 |
rs146159106 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58651556 | TCTATTTTCAAGTCC[A/C]AGCAATTTATGAGAA | 8439 |
rs146232790 | snp | A/C/G | 0.00178266 | 0.0298023 | intron-variant | NSMAF | GRCh38.p7 | 8:58635273 | CAGCTTTTTGGTTGA[A/C/G]GTAAAATTAAACAGT | 8439 |
rs146265969 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58630221 | TTTCTCACAAAGGGA[A/G]TTTGTCCATGTGTTG | 8439 |
rs146351476 | snp | A/G | 9.89201e-05 | 0.00703209 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58589518 | GATCTTACTAACAGC[A/G]TCATCATGTCCCATT | 8439 |
rs146351652 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58616832 | CATGAAAACTCCATG[A/G]AATCTAGCAAAAAAC | 8439 |
rs146386677 | in-del | -/TAAA | 1.65633e-05 | 0.00287774 | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58584065 | GGTTTAAAAATGCAT[-/TAAA]TAGAGTTCAATTTAA | 8439 |
rs146409525 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58657464 | AATCCAATCCATTTG[A/C]TAATTTGTGTTTATT | 8439 |
rs146413959 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58586056 | AGAATGTGGTTTACA[C/T]TATTCTGGATTTTAT | 8439 |
rs146520291 | snp | A/C | 0.380138 | 0.213458 | intron-variant | NSMAF | GRCh38.p7 | 8:58588724 | TGCACGTGGCCGCGG[A/C]CCTTTTTGGCACGAC | 8439 |
rs146530407 | snp | C/T | 0.0379877 | 0.132479 | upstream-variant-2KB, utr-variant-5-prime | NSMAF | GRCh38.p7 | 8:58659797 | GCCGAGAGCCCGACG[C/T]GGCGTCCCGGCCGCG | 8439 |
rs146533360 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58642555 | TTTATAACATTGTCA[C/T]CCGAATAATTGAGAG | 8439 |
rs146594730 | in-del | -/AA | 0.0475351 | 0.146656 | intron-variant | NSMAF | GRCh38.p7 | 8:58585565 | GGGTGTTTTTTGCCC[-/AA]AAAGAGTATGTTCCC | 8439 |
rs146647649 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | NSMAF | GRCh38.p7 | 8:58645788 | GCTCACACCTGTAAT[C/G]CCAGCACTTCGGGAG | 8439 |
rs146669277 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660410 | CATTTACAAGGAAGT[G/T]CACACAAGGACCTGG | 8439 |
rs146767847 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | NSMAF | GRCh38.p7 | 8:58626136 | GTCTCACTGTGTCAC[A/C]CAGGCTGGATGGAGT | 8439 |
rs146901191 | snp | A/G | 0.000131889 | 0.00811956 | missense | NSMAF | GRCh38.p7 | 8:58589547 | TTAACGTGTCCTGGC[A/G]TCTTCCAAATGCTAT | 8439 |
rs146992366 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58651005 | TTTCCAATTGTGTTC[C/T]CTGGGATTTTTTCCT | 8439 |
rs147008504 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58646655 | CTTTAAAATTTTTCT[A/G]TGTAAAAATTATTAT | 8439 |
rs147027400 | snp | A/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661690 | CTGTGAGCCATGATC[A/G]TACCACTGCACCCCA | 8439 |
rs147111951 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NSMAF | GRCh38.p7 | 8:58627610 | CCATTCCTTTTATAA[A/C]AGCTGCAAAAAAAAT | 8439 |
rs147176369 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58641722 | TGTGCATATGTCCAT[G/T]TATATAACTGCCAGT | 8439 |
rs147219674 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | NSMAF | GRCh38.p7 | 8:58606398 | AACATAAATGTCTAG[C/G]TTTCTTTCATAAGTT | 8439 |
rs147254735 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | NSMAF | GRCh38.p7 | 8:58583566 | AATGAAATACAAACC[A/G]TTCCTATACACAGTA | 8439 |
rs147265710 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | NSMAF | GRCh38.p7 | 8:58614513 | AGATAATGGACATCT[C/G]GGTTGCATAGCAATG | 8439 |
rs147272494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58625599 | CTGATATAAGTATGG[C/T]TAGCTCTGTTGTTTG | 8439 |
rs147275100 | snp | G/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58623569 | TTCCTAATATATAGT[G/T]TTTAAACTCAACATT | 8439 |
rs147332065 | snp | C/G | 5.14999e-05 | 0.00507418 | intron-variant | NSMAF | GRCh38.p7 | 8:58586638 | ACATTGATACATATT[C/G]CATTAGATTTATGGT | 8439 |
rs147344169 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58641059 | CCCAAGTAGCTGGGA[C/T]TACAAGGGTGCACCA | 8439 |
rs147432706 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58644820 | GTCCTTTGCAGCGAC[A/G]TGGATGAAGCTGGAA | 8439 |
rs147448493 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58621237 | ATTTGCTCCAGCGCC[A/G]TCCGTGGCCTCCAGC | 8439 |
rs147469873 | snp | A/C | 3.70741e-05 | 0.00430531 | missense | NSMAF | GRCh38.p7 | 8:58631521 | TTATATGGTGCAACA[A/C]CATTATGTTCTTTAA | 8439 |
rs147493861 | snp | C/G | 0.0832709 | 0.186283 | intron-variant | NSMAF | GRCh38.p7 | 8:58656121 | CCTCCCAGGTTCAAG[C/G]AATTCTCCTGCCTCA | 8439 |
rs147537159 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58625423 | ATGTATGTATATATA[C/T]GTGTGAATGTATGTA | 8439 |
rs147582418 | snp | C/T | 0.00269443 | 0.0366054 | intron-variant | NSMAF | GRCh38.p7 | 8:58597575 | AGAACACAAATAATG[C/T]AGTGAACCACTAGGT | 8439 |
rs147591576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58593293 | TTCTATGCTTTGTGG[A/G]AAATTTTTTTATATA | 8439 |
rs147602341 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | NSMAF | GRCh38.p7 | 8:58654321 | AAAGTTGGGCCGGGC[A/G]TGGTGGCTCACCTGA | 8439 |
rs147618593 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58651228 | CTCATTTTATTATCC[A/G]TGTTCTACACATTTG | 8439 |
rs147647770 | snp | C/T | 4.94907e-05 | 0.00497422 | missense | NSMAF | GRCh38.p7 | 8:58594264 | ACTGAAGATCCATTG[C/T]GAGAGACCGTGATTC | 8439 |
rs147657608 | in-del | -/ATAT | | | intron-variant | NSMAF | GRCh38.p7 | 8:58604560 | TAGATATATATAATA[-/ATAT]TATATATATAAACCT | 8439 |
rs147712910 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NSMAF | GRCh38.p7 | 8:58638057 | AAACAATCTGTTTTG[C/T]TTCATTTTAAGAAAT | 8439 |
rs147741715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58632400 | GTCACATGAAGTGCA[C/T]AAGATCTCCACGTCA | 8439 |
rs147816862 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58618419 | TTATTATATATGAGA[C/T]ATATTATGGAATTAT | 8439 |
rs147846446 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58613847 | GCCTCCCTAATCACA[A/T]AATCTGAAATCTGAA | 8439 |
rs147866066 | snp | C/T | 6.62087e-05 | 0.00575326 | missense | NSMAF | GRCh38.p7 | 8:58601498 | GAGTAGTGACTCCCA[C/T]ACATGAACTTTGGTT | 8439 |
rs147897385 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | NSMAF | GRCh38.p7 | 8:58617647 | AATGGCAATCATTAA[A/G]AAGTCAGGAAACAAC | 8439 |
rs147914201 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58613472 | ATAACACAAAGTGCT[A/G]CAGCTAAAAAGTCAA | 8439 |
rs147922619 | snp | C/T | 0.00299725 | 0.0385959 | intron-variant | NSMAF | GRCh38.p7 | 8:58597953 | GCTATTTCAATGTAA[C/T]ATACACTGTTTAGAA | 8439 |
rs147951951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58593724 | CATATCAATGACACA[C/T]TGCAAGGGTTTTTAT | 8439 |
rs147985912 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | NSMAF | GRCh38.p7 | 8:58654959 | CTTGTCTCAGTCTCC[C/T]GAGTAGCTGGGATTA | 8439 |
rs147990005 | snp | A/T | 1.64738e-05 | 0.00286995 | missense | NSMAF | GRCh38.p7 | 8:58597475 | AGGATGTGGTGTCAC[A/T]AATAGTTGTTTTGGT | 8439 |
rs148067365 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | NSMAF | GRCh38.p7 | 8:58600352 | ACCACTGGTAGGGCG[C/T]GGTGGCTCACACCTG | 8439 |
rs148145587 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | NSMAF | GRCh38.p7 | 8:58657869 | GTTCTCTCTGAACAC[C/T]GCCAGCCTATCACGT | 8439 |
rs148148194 | snp | C/T | 3.30437e-05 | 0.00406457 | missense | NSMAF | GRCh38.p7 | 8:58609695 | GTCACCATTTCTGCT[C/T]TGCATTCCATGTGCA | 8439 |
rs148182874 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58651670 | CAGCCTTTTTATATG[C/T]ACTATCAAGAAGTTA | 8439 |
rs148303650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58628090 | AAAGCCAAATACTTA[C/T]AGCCAACTGATCTTT | 8439 |
rs148355171 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58625230 | TTGCATTCAGACTCA[C/G/T]ACTAAACGCTATACC | 8439 |
rs148436988 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58608186 | AACTGGCATAAATAA[C/T]CTCTCAGGAATCTTG | 8439 |
rs148453600 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58623613 | CTACATATTTAGAAA[A/G]CAGATGATGATTTGG | 8439 |
rs148456704 | snp | C/G | 0.00626517 | 0.0556177 | upstream-variant-2KB, missense | NSMAF | GRCh38.p7 | 8:58659589 | TCTCCTTGGAGTAGA[C/G]CTGCAGCTGCTGCTC | 8439 |
rs148557673 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58648026 | GAGACTGGTTAAATG[A/G]TTGTGACCAAAATAC | 8439 |
rs148646550 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | NSMAF | GRCh38.p7 | 8:58645367 | AAAACATGGAATAGA[A/T]GAACACTAGTTTGCT | 8439 |
rs148661666 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58585114 | TAAGCAAACAATCTA[A/G]TGAATCTCCAAGAAA | 8439 |
rs148669315 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58596575 | AACAGATACCCTGTA[A/T]ATGTTTGTCAAATGT | 8439 |
rs148714602 | snp | A/C | 0.0535932 | 0.154675 | intron-variant | NSMAF | GRCh38.p7 | 8:58617379 | TGAACAGGCAACCTA[A/C]AGAATGGGAGAAAAT | 8439 |
rs148783221 | in-del | -/TG | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58612829 | CCCCATCATACACTC[-/TG]AAACCCTCAAGCAGG | 8439 |
rs148818311 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58654708 | ATCACTAATTTCCAT[C/G]CTTGAGTGGAAATCT | 8439 |
rs148862871 | snp | C/T | 0.000132264 | 0.00813109 | missense | NSMAF | GRCh38.p7 | 8:58597396 | ATTTACCTGGGGAAT[C/T]TGCCATAGAAGCATT | 8439 |
rs148870150 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58650946 | TTCCACCCACTTAAC[A/G]TGGCCTGTAACAAAA | 8439 |
rs148946537 | snp | A/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58646001 | AGCCAAGATCGCGCC[A/G]CTGCACTCCAGCCTA | 8439 |
rs148976415 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58657755 | ATAATTCAAATAAAT[A/T]TAAAACACATGGCGC | 8439 |
rs148980935 | snp | A/C | 0.0252325 | 0.109451 | intron-variant | NSMAF | GRCh38.p7 | 8:58586181 | TTCCAAGATGTAAGG[A/C]TGAGATGACCCTTTG | 8439 |
rs148981624 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58598102 | AATCTACTTGTCAGG[G/T]AGAGGACCTGTCATC | 8439 |
rs148997894 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | NSMAF | GRCh38.p7 | 8:58641894 | GTTTCAGTTTGCTAC[A/C]TGTAGTTGTATTTTA | 8439 |
rs149004252 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | NSMAF | GRCh38.p7 | 8:58639325 | AAGAAGAAGAAGACA[C/T]ACAAATGGCCAACAA | 8439 |
rs149019489 | in-del | -/C | 0.178465 | 0.239547 | intron-variant | NSMAF | GRCh38.p7 | 8:58653462 | CCTAAAGCCTTAGGA[-/C]ACAGAATAGTGAAAA | 8439 |
rs149032828 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58620410 | AAGATGCATCATCAA[C/T]GACTAGTAGTAAATA | 8439 |
rs149155175 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58610591 | AGCAACCTAAATGAA[C/T]ATGATTGCAAAAAGG | 8439 |
rs149185722 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | NSMAF | GRCh38.p7 | 8:58624952 | CATACATATGGTGAT[A/G]ATTAATTTTATATGT | 8439 |
rs149202268 | snp | A/G | 0.0185938 | 0.0946107 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58661115 | GGAAGCTAATCCTCC[A/G]TGTTGACTTCTGATT | 8439 |
rs149227756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58603556 | TTGTTCAGCTATGTA[C/T]AAACAGTTCCAAGAT | 8439 |
rs149258877 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58647503 | AATGTGATTCCCAAC[A/G]TTGAAGGTGGAGGCC | 8439 |
rs149300701 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | NSMAF | GRCh38.p7 | 8:58600253 | GTGGGCATAGAGTCC[A/G]AGTCCACACCATTAG | 8439 |
rs149317377 | snp | C/T | 0.131723 | 0.220251 | intron-variant | NSMAF | GRCh38.p7 | 8:58644703 | CACAATAGCAAAGAC[C/T]TGGAACCAACCCAAA | 8439 |
rs149344037 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | NSMAF | GRCh38.p7 | 8:58590783 | ACTCAATTGTTTTGG[A/G]AGAAATAAAGTATTA | 8439 |
rs149346079 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58621163 | GTCCATTTGTACTCA[A/G]TGTTCAGTTCCTACT | 8439 |
rs149360975 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58633987 | ATAACTAAAATGTAT[A/G]GTTTTATAATGAAAA | 8439 |
rs149476649 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | NSMAF | GRCh38.p7 | 8:58611556 | CAACACATGTGAAAA[A/G]ACAGAGTTTCAGCAG | 8439 |
rs149487246 | in-del | -/CAAC | | | intron-variant | NSMAF | GRCh38.p7 | 8:58592911 | CAAAAACAAAAACAA[-/CAAC]AACAAAAAAAAAACC | 8439 |
rs149521321 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58639467 | AACAGTTGTTGGCAA[A/G]AGCGTGGAGAAAAGA | 8439 |
rs149564750 | snp | A/G | 0.0111798 | 0.073925 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58595607 | CAGTTTGGTGATGTT[A/G]TTCCAGGCCAGTGTT | 8439 |
rs149592948 | snp | C/T | 0.00879672 | 0.0657342 | synonymous-codon, intron-variant | NSMAF | GRCh38.p7 | 8:58659236 | GTGCCGGGATCCACG[C/T]CCGGACCCCGCGCGG | 8439 |
rs149643936 | snp | G/T | 0.172997 | 0.237846 | intron-variant | NSMAF | GRCh38.p7 | 8:58655851 | GGCGGAACTTGCAGT[G/T]GGCTGAGATCGTGCC | 8439 |
rs149650758 | snp | C/G/T | 1.64787e-05 | 0.00287038 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58585987 | TGTTCCTGTGCTGAG[C/G/T]ACATGGCGACTATCT | 8439 |
rs149662501 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58592746 | ACAAAAATTAGCCAG[C/G]CACGATGGTGGGTGC | 8439 |
rs149678977 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58637040 | CACACACACACACAC[A/C]CCCACACACAAACAC | 8439 |
rs149714345 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58587574 | CAGCCGAACCCCTAG[A/T]CTTTTAAGGTCAGTT | 8439 |
rs149742903 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | NSMAF | GRCh38.p7 | 8:58654491 | GGAGGCGGAGTTTGC[A/G]GTGAGCCAAGATCAT | 8439 |
rs149787547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58613210 | ATTTCTATGCAAACA[C/T]ATATATGTATCTAAA | 8439 |
rs149890381 | snp | C/G/T | 0.00269863 | 0.0366342 | synonymous-codon, missense | NSMAF | GRCh38.p7 | 8:58597505 | TGTCTGCCCAAATTC[C/G/T]AAGATTTGCGTAAGC | 8439 |
rs149924717 | in-del | -/TAA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58600768 | TATCTCAGTGTGGTG[-/TAA]GGATACCAAGTAAAC | 8439 |
rs149927505 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | NSMAF | GRCh38.p7 | 8:58625677 | TCTGTGTCCTTAAAC[C/T]GAAAATGAGTCTCTT | 8439 |
rs149947487 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58619691 | CCATTTATAATACCA[A/T]CACAAATATGAAGTA | 8439 |
rs149963470 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58657341 | AGAGCCGCCAGTGAA[A/C]TTACAATGAACAGGT | 8439 |
rs149989927 | snp | C/T | 0.0325976 | 0.123435 | intron-variant | NSMAF | GRCh38.p7 | 8:58609387 | AGCAAGTGCCCCTGA[C/T]ATGACTGAAAACAGA | 8439 |
rs149999640 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | NSMAF | GRCh38.p7 | 8:58649926 | GACAACAACTTCCTC[C/T]TCTAGTGGTTTATAA | 8439 |
rs150019202 | snp | C/T | 3.29549e-05 | 0.00405911 | missense | NSMAF | GRCh38.p7 | 8:58599804 | GTCCTCCTTGTCTCT[C/T]TCCCAAATCCAACTT | 8439 |
rs150048294 | snp | A/G | 0.000378903 | 0.0137589 | synonymous-codon | NSMAF | GRCh38.p7 | 8:58603301 | GGCCAGGTTGTTGAG[A/G]TGAAGGAGGTACTGA | 8439 |
rs150104149 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | NSMAF | GRCh38.p7 | 8:58586120 | TTTCTTCAAAATCCT[C/T]GTACTTAAGCAATGA | 8439 |
rs150112584 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | NSMAF | GRCh38.p7 | 8:58615347 | TGGACCCATACGGCA[C/T]TTATGGAATACTATT | 8439 |
rs150120245 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | NSMAF | GRCh38.p7 | 8:58627324 | CAAGGTTACCCACTT[C/T]CACCACTTCTATTCA | 8439 |
rs150150191 | snp | A/C | | | intron-variant | NSMAF | GRCh38.p7 | 8:58644286 | CCCACAGGCTAAAGC[A/C]AATTGGAGAGATATT | 8439 |
rs150271308 | snp | A/G/T | 0.0185938 | 0.0946107 | intron-variant | NSMAF | GRCh38.p7 | 8:58633906 | CTTCTATAAACTATT[A/G/T]AAAAAGTAGGTGGAG | 8439 |
rs150273330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58657924 | CAAAGCAGCATATAC[A/G]TGGAAATGCAAGTAC | 8439 |
rs150306393 | snp | C/T | | | intron-variant | NSMAF | GRCh38.p7 | 8:58611060 | AAATATTATTTAGTT[C/T]GGTCTCAACACTTCC | 8439 |
rs150322945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58651983 | TAAACTTCAAGGATA[C/T]CATAAAAATAAGCAC | 8439 |
rs150323981 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | NSMAF | GRCh38.p7 | 8:58660853 | TCAAGGTTCATCTAT[A/G]TTGTAGCATGTATCT | 8439 |
rs150327850 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58589379 | AATATCTGTATGTAC[A/C]TTTTAAGCTAAAAAT | 8439 |
rs150330925 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | NSMAF | GRCh38.p7 | 8:58603285 | CGTTGCAGCTGCGGT[C/T]GGCCAGGTTGTTGAG | 8439 |
rs150358444 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58605461 | ATTCAATTTGGAGGA[C/T]GTTAAAATATAAGAG | 8439 |
rs150411552 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58639165 | TGGCACGTGCTGTAC[A/G]CCCAGCTACTTGGGA | 8439 |
rs150453888 | in-del | -/CAA | | | intron-variant | NSMAF | GRCh38.p7 | 8:58629640 | TAAAAACAACAACAA[-/CAA]CAACAAAAACAATTA | 8439 |
rs150488651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58594000 | AAAGGAGGCTGTTTC[C/T]GTCCTCTATCCTCAA | 8439 |
rs150591467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58636772 | ATGGCCCAAGGGCTG[C/T]AGTTTGCCAAGCCCT | 8439 |
rs150636426 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58654069 | CTTTAAGTCACAGTC[A/G]GATAGATTTCTTGGG | 8439 |
rs150658367 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | NSMAF | GRCh38.p7 | 8:58608524 | GGAAACTGCCCCGGA[G/T]TCCCAGAGTCAGGTC | 8439 |
rs150658908 | snp | C/T | 0.000231512 | 0.0107565 | missense | NSMAF | GRCh38.p7 | 8:58623250 | GATGTTCTAGCTAAA[C/T]GAGACTGCAAAATAG | 8439 |
rs150692077 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | NSMAF | GRCh38.p7 | 8:58621147 | TTGTTCCCTTCTTTG[C/T]GTCCATTTGTACTCA | 8439 |
rs150719986 | snp | A/G | 0.000181271 | 0.00951855 | missense | NSMAF | GRCh38.p7 | 8:58584128 | TGCAATTTCCAGAAT[A/G]TAATTTGTCTGTCTT | 8439 |
rs150775141 | in-del | -/CT | | | intron-variant | NSMAF | GRCh38.p7 | 8:58598848 | CCAACATGGTGAAAC[-/CT]CGTCACGACCAAAAA | 8439 |
rs150791010 | in-del | -/T | 0.172997 | 0.237846 | intron-variant | NSMAF | GRCh38.p7 | 8:58655477 | GACCATAGCTCACTG[-/T]TAACCTTGGACTCCT | 8439 |
rs150799495 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58597188 | ATAAAAGCGATTTGA[C/T]TTCCCTTACAGTCTA | 8439 |
rs150850146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58587363 | GCTCAGAAACTACTA[C/T]TTTGGAATTCTAGTT | 8439 |
rs150870126 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58645666 | ACAATGCAGAGAACA[A/G]AAGAAAAGGTCAAAA | 8439 |
rs150898090 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | NSMAF | GRCh38.p7 | 8:58655329 | CCAACACTCCACGGT[A/G]GATAGTAAAGCAAAA | 8439 |
rs150902909 | snp | C/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SDCBP, NSMAF | GRCh38.p7 | 8:58583189 | TAGTGTGGTCTGACT[C/G]AAGTTTTTTCTCCTA | 8439 |
rs150953038 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58626837 | CCAGCAGTGTAAAAG[C/T]GCTCCCTTTTCACCA | 8439 |
rs150970885 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58610769 | ATGCTGTCGACTGAG[G/T]TGCAAAACAAGGGAA | 8439 |
rs150981925 | snp | A/G | 0.306679 | 0.24349 | intron-variant | NSMAF | GRCh38.p7 | 8:58639300 | ATAAAAAAAAAAAAA[A/G]AAGAAGAAGAAGAAG | 8439 |
rs151004766 | snp | A/G/T | 0.00319106 | 0.0398404 | intron-variant | NSMAF | GRCh38.p7 | 8:58623866 | ATGTGTACAGAACCT[A/G/T]CTATGATAAAATCTG | 8439 |
rs151015572 | in-del | -/ACGAA/CGAA/GA/TT | 0.443908 | 0.157796 | intron-variant | NSMAF | GRCh38.p7 | 8:58623301 | CCAGAAAAAAAGTAT[-/ACGAA/CGAA/GA/TT]TTATAAGTATTTATA | 8439 |
rs151028316 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | NSMAF | GRCh38.p7 | 8:58612710 | AGGCAGACAATGAAT[C/G/T]GAATTGTAGAATACC | 8439 |
rs151047902 | snp | A/G | 1.66838e-05 | 0.00288818 | missense | NSMAF | GRCh38.p7 | 8:58590022 | ACATTATTATCCCAT[A/G]AAGAAGTTATGACAG | 8439 |
rs151164453 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | NSMAF | GRCh38.p7 | 8:58589369 | AGTGGCTTATAATAT[C/T]TGTATGTACATTTTA | 8439 |
rs151180209 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | NSMAF | GRCh38.p7 | 8:58632001 | GTCCTTACATAGTAT[A/G]TTAATAACTATGTGG | 8439 |
rs151184016 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58646037 | CAAGAGCGAGACTCC[A/G]TCTCAAAATCATCAT | 8439 |
rs151206159 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | NSMAF | GRCh38.p7 | 8:58603272 | TACTGGGAGAGGTCG[C/T]TGCAGCTGCGGTCGG | 8439 |
rs151218098 | snp | A/G | 0.0162398 | 0.0886349 | intron-variant | NSMAF | GRCh38.p7 | 8:58656857 | ATAAAAAAAATTAGT[A/G]TAAGTATATACCAAA | 8439 |
rs151241201 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58649446 | CTATTGGGAAGAAAT[G/T]ATTGTATTTTCCAAT | 8439 |
rs151337681 | snp | C/G | 0.0599851 | 0.162463 | intron-variant | NSMAF | GRCh38.p7 | 8:58639083 | AGATCAGGAGATCGA[C/G]ACCATCCTGGCTAAC | 8439 |
rs180829573 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58628290 | TAAAAATTCTACATG[A/G]TAATATTGGAAAAAC | 8439 |
rs180833557 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58612894 | ACAGCAATTCAAATC[A/G]TGGGGCTCTTCACCG | 8439 |
rs180833723 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58639355 | AGCATATGAAAAGAT[A/C]CTCAGCAGCCTTAAT | 8439 |
rs180834416 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58655150 | GGCCTATTTATTTTT[G/T]AAATAGAGAAAAGGT | 8439 |
rs180844868 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58602410 | TCTGATTAAGGAACA[C/T]ATATATATTCCAAGT | 8439 |
rs180848184 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | NSMAF | GRCh38.p7 | 8:58592465 | ACATACCTAAACATA[C/T]TGTATACTAGAAGAA | 8439 |
rs180864351 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58622541 | TAGGATTACAGGTGC[C/T]CGCCACCATGCCTGG | 8439 |
rs181056367 | snp | A/G | | | intron-variant | NSMAF | GRCh38.p7 | 8:58625678 | CTGTGTCCTTAAACC[A/G]AAAATGAGTCTCTTG | 8439 |
rs181059552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58649776 | CACCTTCCACCATGA[A/G]TAAAAGCTCCCTGAG | 8439 |
rs181066202 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | NSMAF | GRCh38.p7 | 8:58606881 | AAATGAAACATTATA[C/T]ATAAATTGCCTGTTA | 8439 |
rs181073134 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58633635 | GAGCCCTGAATATAA[C/T]ACTTATTGAATCCAT | 8439 |
rs181075508 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58586926 | TAAATTATAGTGAGC[C/T]GCCAAAGTGCCTGAA | 8439 |
rs181078156 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | NSMAF | GRCh38.p7 | 8:58617608 | AATCAAAACCACAAC[A/G]AGATACCATCTCATG | 8439 |
rs181106136 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58657199 | AGTCAGTCTCTATGC[C/T]TCTGCTTTTGCAGGA | 8439 |
rs181119457 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58643175 | GCTTTTCCATTCTTG[A/C]ATTTAACAAACATTT | 8439 |
rs181166254 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58597665 | CAAATAATGACAGCA[A/G]CTATGTACCAGGATT | 8439 |
rs181280024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58646119 | AAATGATAGCAGAAA[C/T]CAATTTTACCATCCT | 8439 |
rs181281545 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58629007 | TCTGATTATCATGTG[A/T]CTTGGTAAGGACATC | 8439 |
rs181297328 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58613359 | AAATACATTGGAGTA[A/T]GGTTCTTGTATTGGT | 8439 |
rs181399024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58593417 | TGAAAGTGTTTAGTT[A/G]GATAGCACTTTGTCT | 8439 |
rs181414322 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58620671 | ACAGGCATTTAAATT[A/T]ACTGTTATTGAAAAC | 8439 |
rs181528893 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58637965 | AAACCCTATTAAAAT[C/T]CCAATGGCATTTTTA | 8439 |
rs181540899 | snp | A/C | 0.000727082 | 0.0190529 | intron-variant | NSMAF | GRCh38.p7 | 8:58601234 | ACAAGTATGTTGTAT[A/C]TATACAATCAGAAAG | 8439 |
rs181584517 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | NSMAF | GRCh38.p7 | 8:58656697 | TAGCCGGGCGTGGTG[A/G]CAGGCGCCTGTAGTC | 8439 |
rs181600101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58641780 | GCATTGCTAGATCAA[C/T]AGGTTAATGCACATG | 8439 |
rs181602009 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58624895 | CTCCCTTCAGTTCTA[C/T]CAATGTTCGCTTCAT | 8439 |
rs181604893 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | NSMAF | GRCh38.p7 | 8:58605784 | ACTCGGGAGGCTGAG[A/G]CACAAGAATCACTTG | 8439 |
rs181615215 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | NSMAF | GRCh38.p7 | 8:58584940 | GCCCAGACTTTTTAA[G/T]GTATACATTTAAGAA | 8439 |
rs181706670 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | NSMAF | GRCh38.p7 | 8:58634152 | CCAGAGCAGTAGATG[G/T]TTGTCACTGTCTTCA | 8439 |
rs181721905 | snp | A/C | 0.0040129 | 0.0446133 | intron-variant | NSMAF | GRCh38.p7 | 8:58597840 | ACTCAAGTAGAAACT[A/C]CTTATTGACATATAA | 8439 |
rs181785544 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58654593 | TACTAGCATAATCAA[A/G]AATATTATACACTCA | 8439 |
rs181800391 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58638910 | ATACATAAAAAACTC[A/G]AACAACTTGATAGTA | 8439 |
rs181805347 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58650475 | AGCTTCCTTCCAACA[G/T]GCAAGCTTGCCTGAT | 8439 |
rs181810828 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58621965 | CTGTTTAAAAGCTCT[G/T]TAGTTTAATTAGTTC | 8439 |
rs181821805 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | NSMAF | GRCh38.p7 | 8:58601825 | ACAGAATGCCTTCAT[C/G]AAAATAATTCAGTGA | 8439 |
rs181851130 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | NSMAF | GRCh38.p7 | 8:58618021 | TTGCAGGGACATGGA[C/T]GAAGCTGGAAACCAT | 8439 |
rs181978585 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | NSMAF | GRCh38.p7 | 8:58611015 | AAGTAGCCTGACAGA[A/G]TAAGAGGTGGCTTGA | 8439 |
rs181995138 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | NSMAF | GRCh38.p7 | 8:58651430 | TCTATCACTCAGCTG[C/G]ACTCTAGAAAATTAC | 8439 |