SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs759352 | snp | A/C/G | 0.0310518 | 0.120672 | intron-variant | FANCL | GRCh38.p7 | 2:58187981 | CAGATATTTCTTAGT[A/C/G]TAACACCAAATGCAA | 55120 |
rs768298 | snp | A/G | 0.497776 | 0.0332724 | intron-variant | FANCL | GRCh38.p7 | 2:58183837 | ATCAGAGAAGCCAAC[A/G]TAGTCCTGTACATGG | 55120 |
rs848278 | snp | C/T | 0.365853 | 0.221536 | intron-variant | FANCL | GRCh38.p7 | 2:58193750 | CCCCTAGTTTTTCAC[C/T]GTAATAATCCTGTGG | 55120 |
rs848279 | snp | G/T | 0.376592 | 0.215579 | intron-variant | FANCL | GRCh38.p7 | 2:58192514 | tgtaatgtggttaac[G/T]gtgattaattttcct | 55120 |
rs848280 | snp | A/G | 0.373397 | 0.217424 | intron-variant | FANCL | GRCh38.p7 | 2:58185337 | GATCTTTTCATGGAC[A/G]AGCCCGTATACGGAA | 55120 |
rs848281 | snp | A/T | 0.381308 | 0.21274 | intron-variant | FANCL | GRCh38.p7 | 2:58181934 | ATAGATTTGAAGATT[A/T]ATTTTAAAAGGCCAG | 55120 |
rs848282 | snp | A/G | 0.38286 | 0.211774 | intron-variant | FANCL | GRCh38.p7 | 2:58181552 | TCAAAATATGTCATC[A/G]GCATGCATACATTTA | 55120 |
rs848283 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FANCL | GRCh38.p7 | 2:58180612 | tgcacccatcaaccc[A/G]acatctacattaggt | 55120 |
rs848284 | snp | A/T | 0.379158 | 0.214052 | intron-variant | FANCL | GRCh38.p7 | 2:58211905 | ctagagactagttgc[A/T]tggctttgcccaaaa | 55120 |
rs848285 | snp | A/C | 0.405082 | 0.196086 | intron-variant | FANCL | GRCh38.p7 | 2:58168146 | ttgccagccaccAAG[A/C]ATGTTAGCtattttt | 55120 |
rs848286 | snp | A/G | 0.455502 | 0.142369 | intron-variant | FANCL | GRCh38.p7 | 2:58167408 | GACAGAGAAAGGAGA[A/G]ACAGAGATATACTAT | 55120 |
rs848287 | snp | A/G | 0.378174 | 0.214642 | intron-variant | FANCL | GRCh38.p7 | 2:58166776 | CATGTTTAAGGAAGT[A/G]GCTAGTTTCTTTTCA | 55120 |
rs848288 | snp | A/G | 0.400325 | 0.199756 | intron-variant | FANCL | GRCh38.p7 | 2:58165654 | AAAATAAATCTAACA[A/G]TGACAGTTGGACTCA | 55120 |
rs848289 | snp | A/T | 0.402982 | 0.197728 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164435 | GTTCATAGTAAATAA[A/T]GTGTTACCAAATGAG | 55120 |
rs848290 | snp | A/T | 0.0836354 | 0.186609 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162047 | TTTTTGGCTGGCAAG[A/T]TGTTTGGGCATCAGT | 55120 |
rs848291 | snp | C/T | 0.455798 | 0.14194 | synonymous-codon, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161561 | AGTGTGTGATAATTC[C/T]CAGTGTGGACAACCT | 55120 |
rs1011314 | snp | A/G | 0.499722 | 0.0117779 | intron-variant | FANCL | GRCh38.p7 | 2:58195857 | ctttggggttacgca[A/G]tattgacaaattgcc | 55120 |
rs1100188 | snp | G/T | 0.378568 | 0.214407 | intron-variant | FANCL | GRCh38.p7 | 2:58188980 | cttttttccttggca[G/T]aattacttggagatt | 55120 |
rs1100189 | snp | C/G | 0.383632 | 0.211288 | intron-variant | FANCL | GRCh38.p7 | 2:58175346 | atcaaggatattggt[C/G]taaaattctcttttt | 55120 |
rs1100190 | snp | C/G | 0.380333 | 0.213338 | intron-variant | FANCL | GRCh38.p7 | 2:58172770 | ctgtccagctttgtt[C/G]cattgctggtgagga | 55120 |
rs1100191 | snp | C/T | 0.376989 | 0.215346 | intron-variant | FANCL | GRCh38.p7 | 2:58169085 | agcagagctcgagtg[C/T]tgtggtgggagatct | 55120 |
rs1404457 | snp | A/T | 0.192715 | 0.243348 | intron-variant | FANCL | GRCh38.p7 | 2:58205749 | CCAGCTGTTTCTGCC[A/T]GGAGTCCTTGTTCTC | 55120 |
rs1404458 | snp | G/T | 0.0271762 | 0.113356 | intron-variant | FANCL | GRCh38.p7 | 2:58204465 | CACTGACCACAGCAT[G/T]AGCCTTGACACACAT | 55120 |
rs1404459 | snp | C/G | 0.220304 | 0.24823 | intron-variant | FANCL | GRCh38.p7 | 2:58204275 | ATCTCCAGTTCCCCT[C/G]TCCAGCTCTCCCCGG | 55120 |
rs1404460 | snp | A/G | 0.291235 | 0.246576 | intron-variant | FANCL | GRCh38.p7 | 2:58204033 | TGCTAGTTACATCTA[A/G]AAATACATATATCAT | 55120 |
rs1404461 | snp | A/C | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58202067 | CCTGCGATTGTCAGT[A/C]AACTACACTAATAGT | 55120 |
rs1524856 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | FANCL | GRCh38.p7 | 2:58213270 | ACTGTTTAAGGCCCC[A/G]CCTGAGGAGCTGGCT | 55120 |
rs1830016 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202369 | AAAAAAAAGTTAGTT[C/T]TAGATTGTGAATTTG | 55120 |
rs2098344 | snp | A/G | 0.494315 | 0.0530107 | intron-variant | FANCL | GRCh38.p7 | 2:58186616 | AGTGGCATGGAAGCC[A/G]GAAAAAAATGCTCTT | 55120 |
rs2110664 | snp | G/T | 0.494936 | 0.050064 | intron-variant | FANCL | GRCh38.p7 | 2:58235596 | ctagacataatgaat[G/T]ctacctgttgcatgc | 55120 |
rs2192690 | snp | G/T | 0.318415 | 0.240457 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243207 | TCCATGGGGGAAAGT[G/T]TGGTGGTGGGGAAGT | 55120 |
rs2691672 | snp | C/T | 0.379158 | 0.214052 | intron-variant | FANCL | GRCh38.p7 | 2:58178125 | gtgaatctgtgtggt[C/T]ctgggctttttttgg | 55120 |
rs3217126 | in-del | -/TTAT | | | intron-variant | FANCL | GRCh38.p7 | 2:58204344 | CAGAAATTGCTCTGA[-/TTAT]TTTTTATAATGGATT | 55120 |
rs3732136 | snp | C/T | 0.493881 | 0.054972 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159865 | TAAAATTGCTTTGTA[C/T]TAGAAATAGTGTCAT | 55120 |
rs3732137 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58159874 | TTTGTACTAGAAATA[C/G]TGTCATAGAATAGTG | 55120 |
rs3755296 | snp | A/G | 0.193653 | 0.243567 | intron-variant | FANCL | GRCh38.p7 | 2:58185833 | TGACTAGGGAATATA[A/G]TTTTAGTCAAGGAGT | 55120 |
rs3755297 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58194957 | ATAAAGATCTTCCAA[C/G]TTTAAAGTCCAGAAA | 55120 |
rs3771216 | snp | C/T | 0.499977 | 0.00339449 | intron-variant | FANCL | GRCh38.p7 | 2:58184705 | CAATAAACTGTCTTA[C/T]AGGAAGAAAAGTATC | 55120 |
rs3771218 | snp | C/T | 0.0689305 | 0.172377 | intron-variant | FANCL | GRCh38.p7 | 2:58197125 | TTTTGCTATGTTTTC[C/T]CAACTTCCATTGTGG | 55120 |
rs3771219 | snp | A/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58215166 | ATCTATACCTAAAGA[A/G]TGACTAGGTCCATGA | 55120 |
rs3771220 | snp | C/T | 0.425432 | 0.178112 | intron-variant | FANCL | GRCh38.p7 | 2:58223434 | ATTAATTATTGCTAT[C/T]CACAAAAATTGAAGG | 55120 |
rs3771221 | snp | A/T | 0.379158 | 0.214052 | intron-variant | FANCL | GRCh38.p7 | 2:58224098 | ATTGTAAATCAGAGA[A/T]CTCAAAATTTTATTT | 55120 |
rs3771222 | snp | C/T | 0.19334 | 0.243495 | intron-variant | FANCL | GRCh38.p7 | 2:58229142 | ATCATAGATAATAAC[C/T]TGCCTTTAAGACACA | 55120 |
rs3771223 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58231890 | ACAGGTAAATATTTA[C/T]AAATGCTGCATTGGT | 55120 |
rs3771224 | snp | C/T | 0.377582 | 0.214995 | intron-variant | FANCL | GRCh38.p7 | 2:58232894 | AATCTTTTACTCTAA[C/T]AGAATAAAATGAAAA | 55120 |
rs3771225 | snp | C/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58233883 | AAAGATAGGTAGAGA[C/G]ACCTTTTGGAAACTG | 55120 |
rs3821210 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58198050 | gtgtgtgtgtgcgtg[C/T]gtgtgtgtgtatata | 55120 |
rs3821211 | snp | A/T | 0.0729998 | 0.176553 | intron-variant | FANCL | GRCh38.p7 | 2:58204574 | ATTAAACTTCCTGTC[A/T]AACTCTTTGATCCAT | 55120 |
rs3821212 | snp | A/T | 0.409041 | 0.192888 | intron-variant | FANCL | GRCh38.p7 | 2:58216463 | AGGTACACTAACTAG[A/T]ATGCCTCCAAATTAA | 55120 |
rs3821213 | snp | C/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58222658 | TAAAATGTTTATGTT[C/T]TCCCAACCAAAACTA | 55120 |
rs3834164 | in-del | -/A | 0.375 | 0.216506 | intron-variant | FANCL | GRCh38.p7 | 2:58194927 | TGTCTATTATATCAC[-/A]AAAAAAAAAAGAAAA | 55120 |
rs3836117 | in-del | -/TAC | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58166166 | AATAGTAATGAGTAC[-/TAC]AAGATGTATGTACAC | 55120 |
rs3836118 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58194130 | TCCATGATAAAAAAA[-/A]TATAAAGACCACTAT | 55120 |
rs3836119 | in-del | -/GTAAAA | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58205364 | TCTTAGAAAACAAAA[-/GTAAAA]CTATTCTAGAAAGTG | 55120 |
rs3836120 | in-del | -/T | 0.259618 | 0.249815 | intron-variant | FANCL | GRCh38.p7 | 2:58223008 | TTAAGTATATATCAA[-/T]TTTTTTTAACCAGGA | 55120 |
rs3836121 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58223019 | CAATTTTTTTTAACC[-/C]AGGATAGGACACTAT | 55120 |
rs3836122 | in-del | -/C | 0.490453 | 0.0684267 | intron-variant | FANCL | GRCh38.p7 | 2:58233253 | AGAAGAACTATTCTA[-/C]TATAGAAATCTGTGC | 55120 |
rs4395240 | snp | C/G | 0.307176 | 0.243374 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242365 | TGATCCTAGAACCTA[C/G]CAACAGCATCACCTG | 55120 |
rs4672231 | snp | A/G | 0.382666 | 0.211895 | intron-variant | FANCL | GRCh38.p7 | 2:58175134 | ctctgaaattgtggc[A/G]aaaatcaatagctta | 55120 |
rs4672232 | snp | A/T | 0.382666 | 0.211895 | intron-variant | FANCL | GRCh38.p7 | 2:58175136 | ctgaaattgtggcga[A/T]aatcaatagcttacc | 55120 |
rs5831491 | in-del | -/AA | | | intron-variant | FANCL | GRCh38.p7 | 2:58202250 | AAAAAAAAAAAAAAA[-/AA]GACTTCCTGGTTTTC | 55120 |
rs6709203 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | FANCL | GRCh38.p7 | 2:58194524 | AAAGCAAATATCTAG[A/G]AAGAGGTGCTTAGAC | 55120 |
rs6709460 | snp | C/G | 0.377187 | 0.215229 | intron-variant | FANCL | GRCh38.p7 | 2:58217475 | GGAAGAATTTCAATA[C/G]AGCATTAAAATCTGT | 55120 |
rs6709533 | snp | A/T | 0.290718 | 0.246662 | intron-variant | FANCL | GRCh38.p7 | 2:58208408 | TATAAGTTAAATTTT[A/T]TAAACATTTAAAATG | 55120 |
rs6717332 | snp | G/T | 0.0667028 | 0.170006 | intron-variant | FANCL | GRCh38.p7 | 2:58218945 | agtataaacacattt[G/T]ttttccatttttcag | 55120 |
rs6721991 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | FANCL | GRCh38.p7 | 2:58220673 | TATGTTCCTTGTTCT[C/T]TTTTAAATGGCGATT | 55120 |
rs6724359 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217201 | atatatatatatata[C/T]atatatatatatata | 55120 |
rs6725148 | snp | C/T | 0.3742 | 0.216966 | intron-variant | FANCL | GRCh38.p7 | 2:58220950 | gggcgtggtggctca[C/T]gcctgtaatcccagc | 55120 |
rs6729598 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | FANCL | GRCh38.p7 | 2:58167860 | TTCAACGAACTTAGG[A/G]GGTAGACATCAAAAC | 55120 |
rs6732503 | snp | A/C | 0.0482946 | 0.147699 | intron-variant | FANCL | GRCh38.p7 | 2:58235590 | tatctagcatgcaac[A/C]ggtagcattcattat | 55120 |
rs6732505 | snp | C/G | 0.394997 | 0.203657 | intron-variant | FANCL | GRCh38.p7 | 2:58228123 | ATAATTGTGATTTTT[C/G]TCCTCTCACAACTAA | 55120 |
rs6735296 | snp | A/T | 0.307423 | 0.243316 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241625 | TGTTTTACTTTATTG[A/T]AAGACTGTTACAACT | 55120 |
rs6740373 | snp | C/T | 0.11963 | 0.213316 | intron-variant | FANCL | GRCh38.p7 | 2:58230229 | ATATAATGTATCAAA[C/T]ATGTATTTGAAAAAG | 55120 |
rs6740836 | snp | C/G | 0.11963 | 0.213316 | intron-variant | FANCL | GRCh38.p7 | 2:58230570 | TACTATTAAGTAACT[C/G]TTCTAAGGAATTACT | 55120 |
rs6741122 | snp | G/T | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58191558 | TGGTGAGATTGACCA[G/T]GATTTTTCATTAATC | 55120 |
rs6742445 | snp | A/T | 0.12932 | 0.218944 | intron-variant | FANCL | GRCh38.p7 | 2:58218738 | ctgaacaattaagta[A/T]atggataacagataa | 55120 |
rs6747314 | snp | A/T | 0.11963 | 0.213316 | intron-variant | FANCL | GRCh38.p7 | 2:58167985 | CCAAATTGAAAAAAA[A/T]AAATTATTTCTAAAT | 55120 |
rs6748725 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58232442 | ATTTCAGTGTTATTT[C/T]TTAGTAAATAAATTT | 55120 |
rs6752935 | snp | A/G | 0.275732 | 0.248672 | intron-variant | FANCL | GRCh38.p7 | 2:58173181 | gtacctgaaagtgac[A/G]aggacaatggaacca | 55120 |
rs6761301 | snp | A/C | 0.499961 | 0.0043928 | intron-variant | FANCL | GRCh38.p7 | 2:58228537 | GGCATGTAGCCATAC[A/C]CATTCACTTACCTCT | 55120 |
rs7340157 | snp | C/T | 0.353154 | 0.227726 | intron-variant | FANCL | GRCh38.p7 | 2:58176490 | gcatatctacaacta[C/T]ctgatcgttgacaaa | 55120 |
rs7340170 | snp | C/T | 0.126909 | 0.217598 | intron-variant | FANCL | GRCh38.p7 | 2:58178232 | ctccctaactcattt[C/T]atgaggcctgcatca | 55120 |
rs7558066 | snp | C/T | 0.306927 | 0.243432 | intron-variant | FANCL | GRCh38.p7 | 2:58181108 | ttaccggaatgctca[C/T]agcagctacattcat | 55120 |
rs7561771 | snp | A/T | 0.318174 | 0.240525 | intron-variant | FANCL | GRCh38.p7 | 2:58233129 | GTAACAATAATTCAC[A/T]GTTTCATTAAAGCAC | 55120 |
rs7577402 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | FANCL | GRCh38.p7 | 2:58209518 | CTATTATGTTTTACA[A/G]AAAATTATCATTATT | 55120 |
rs7578766 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188286 | tatgaaaataccata[A/T]tatcctgaaaaaagt | 55120 |
rs7580070 | snp | A/C | 0.0479149 | 0.147179 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162522 | taaccaaatgcagat[A/C]aaaaatacagtactg | 55120 |
rs7581091 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58240533 | aactagaaaatggga[A/G]tgatgattcttttaa | 55120 |
rs7594702 | snp | C/G | 0.415891 | 0.18703 | intron-variant | FANCL | GRCh38.p7 | 2:58226485 | TTTCTTCACCACCTG[C/G]CCAACACTAGTGTCA | 55120 |
rs7597069 | snp | C/T | 0.120326 | 0.21374 | intron-variant | FANCL | GRCh38.p7 | 2:58193030 | AAATTTTAAAATACT[C/T]AAGAAAAAATTCAAC | 55120 |
rs7599987 | snp | G/T | 0.0704125 | 0.17392 | intron-variant | FANCL | GRCh38.p7 | 2:58238262 | gaagccaaaagattg[G/T]acacccTGTTTTAGA | 55120 |
rs7603404 | snp | G/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58230092 | AATCAGTAAATGACA[G/T]GCAAACAGTACATCT | 55120 |
rs9309303 | snp | A/C | 0.108524 | 0.206118 | intron-variant | FANCL | GRCh38.p7 | 2:58164812 | GTTCCAAATTAAACA[A/C]AGTTAGACTTTTTGA | 55120 |
rs9677908 | snp | C/T | 0.106987 | 0.205054 | intron-variant | FANCL | GRCh38.p7 | 2:58173506 | taaagaaaagaattt[C/T]caacccagaatttca | 55120 |
rs9678508 | snp | A/T | 0.103082 | 0.202275 | intron-variant | FANCL | GRCh38.p7 | 2:58173254 | ccaatctagcaaggc[A/T]ggccaacattcagat | 55120 |
rs10178325 | snp | A/G | 0.113685 | 0.209567 | intron-variant | FANCL | GRCh38.p7 | 2:58187220 | cacatatacaccatg[A/G]aatactatgcagcca | 55120 |
rs10179025 | snp | A/C | 0.039522 | 0.134904 | intron-variant | FANCL | GRCh38.p7 | 2:58212204 | caaagaggagcaagt[A/C]ccatcttacatggat | 55120 |
rs10184957 | snp | G/T | 0.435694 | 0.167385 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159112 | AAGAGATGGCCTACT[G/T]ACGTGGTTTAAAAGA | 55120 |
rs10185190 | snp | A/C | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58189548 | AGATATATGTGAGAA[A/C]TAAGATGTTAGCTAT | 55120 |
rs10185542 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | FANCL | GRCh38.p7 | 2:58184000 | CAACTTCTAAGGTAA[C/T]TTCTAAGGTGACTTC | 55120 |
rs10185758 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | FANCL | GRCh38.p7 | 2:58184231 | TTTAATATACAATAA[C/T]AATTTACTCTTTGAT | 55120 |
rs10445895 | snp | C/T | 0.14052 | 0.224754 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163403 | GATTTTATGACTCTA[C/T]TAAAAAACGTTTAAA | 55120 |
rs10445896 | snp | A/G | 0.176376 | 0.238918 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163412 | ACTCTATTAAAAAAC[A/G]TTTAAATCTCAGATG | 55120 |
rs10490253 | snp | A/G | 0.135825 | 0.222405 | intron-variant | FANCL | GRCh38.p7 | 2:58186559 | TGAGGAACTTTTTCT[A/G]CAGCTGCTTACATAG | 55120 |
rs11125745 | snp | C/G | 0.328148 | 0.237472 | intron-variant | FANCL | GRCh38.p7 | 2:58193787 | CCCAACACTGTGTTT[C/G]TTTTAAACTCGATTT | 55120 |
rs11427269 | in-del | -/A | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58215705 | CAAAAAAAAAAAAAA[-/A]GCATCATTTCCGCCA | 55120 |
rs11461396 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58228071 | TTAACAATATGGTCA[-/T]TTTTTTTTATTTTTC | 55120 |
rs11539575 | snp | A/G | 0.0266805 | 0.112376 | synonymous-codon, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160123 | CTTACTACAATATGG[A/G]CATTCACCAAATATG | 55120 |
rs11687051 | snp | A/T | 0.203575 | 0.245652 | intron-variant | FANCL | GRCh38.p7 | 2:58179465 | tctttgacaaacatg[A/T]caaaaacaagcaatg | 55120 |
rs11692859 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | FANCL | GRCh38.p7 | 2:58216413 | GCACTGAAGTCTGAA[C/T]AGCCAAGGGCAAATG | 55120 |
rs11888277 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58237341 | agaaaatccttaata[C/T]tgagaaagataatca | 55120 |
rs11889211 | snp | A/G | 0.302936 | 0.244331 | intron-variant | FANCL | GRCh38.p7 | 2:58236406 | GAATCCtaatattac[A/G]ttaaggcagaccatg | 55120 |
rs11900900 | snp | A/C | 0.103438 | 0.202533 | intron-variant | FANCL | GRCh38.p7 | 2:58182521 | TTTATTCCTGCGATA[A/C]ATTTTGGAATTTTTG | 55120 |
rs11903212 | snp | C/T | 0.291235 | 0.246576 | intron-variant | FANCL | GRCh38.p7 | 2:58196177 | GGCAAAAAGTATGCA[C/T]GGATGGCCTATATAC | 55120 |
rs11903456 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | FANCL | GRCh38.p7 | 2:58166701 | GTCACATACTACAAA[C/T]GTTTTCAATCTGAAA | 55120 |
rs12468923 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58170754 | acagactttaaacca[A/C]caaagatcaaaagag | 55120 |
rs12469873 | snp | A/G | 0.339203 | 0.233544 | intron-variant | FANCL | GRCh38.p7 | 2:58171205 | atcaaattagaactc[A/G]ggattaagaaactca | 55120 |
rs12470316 | snp | C/T | 0.499859 | 0.0083854 | intron-variant | FANCL | GRCh38.p7 | 2:58219374 | AAATGACTGAAAAAA[C/T]AAATAAATGAGAGGG | 55120 |
rs12474593 | snp | C/T | 0.147321 | 0.227941 | intron-variant | FANCL | GRCh38.p7 | 2:58219532 | gagagaaaaaaacag[C/T]aactttacggtgcag | 55120 |
rs12475594 | snp | A/G | 0.305186 | 0.243833 | intron-variant | FANCL | GRCh38.p7 | 2:58206240 | TAAAAAAGAAAAGCA[A/G]AAGAGAAATAATACA | 55120 |
rs12476829 | snp | C/T | 0.133777 | 0.221342 | intron-variant | FANCL | GRCh38.p7 | 2:58200233 | AAACAATTTGTATGC[C/T]ATATTTAAAAATCGT | 55120 |
rs12477242 | snp | C/G | 0.37955 | 0.213815 | intron-variant | FANCL | GRCh38.p7 | 2:58225657 | GTAATCTCATaagaa[C/G]aaatgaatccaaatc | 55120 |
rs12624152 | snp | G/T | 0.20257 | 0.245465 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163544 | CAAGATTAAATCTTT[G/T]AGAAGTAGAACAGCT | 55120 |
rs12713376 | snp | A/G | 0.275464 | 0.2487 | intron-variant | FANCL | GRCh38.p7 | 2:58175285 | cctaactcattttat[A/G]aggccagcatcattc | 55120 |
rs12988249 | snp | A/G | 0.188946 | 0.24243 | intron-variant | FANCL | GRCh38.p7 | 2:58238103 | ctggcagcccaggac[A/G]gctctgaatgcagcc | 55120 |
rs12995681 | snp | C/T | 0.394354 | 0.204112 | intron-variant | FANCL | GRCh38.p7 | 2:58178933 | agcattcttatacac[C/T]aataacagacaaaca | 55120 |
rs12996821 | snp | A/C | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58239790 | acatacatatactta[A/C]caatgatcagtaaaa | 55120 |
rs13005969 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58205725 | TGGCTGATAAAACAG[A/C]AAAGAAGAGAGAACA | 55120 |
rs13006005 | snp | C/T | 0.194902 | 0.243853 | intron-variant | FANCL | GRCh38.p7 | 2:58196508 | AAAACAAAACTTGTA[C/T]GACCCAATTAAACCT | 55120 |
rs13006338 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58205856 | AAAGGGGGAAGAAGA[A/C]ACTTTAAACCAAATT | 55120 |
rs13015123 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217217 | atatatatatatata[C/T]acacacacacacaca | 55120 |
rs13015126 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58217219 | atatatatatataca[A/C]acacacacacacaca | 55120 |
rs13023069 | snp | C/G/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58239686 | ctcgttcttatgaaa[C/G/T]gtatgctcaagtatt | 55120 |
rs13023405 | snp | A/T | 0.191775 | 0.243125 | intron-variant | FANCL | GRCh38.p7 | 2:58188838 | agatcaatttggaga[A/T]aattTtactagccaa | 55120 |
rs13028673 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219171 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 55120 |
rs13028922 | snp | G/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58210061 | ATAAATAATATATTG[G/T]TTAAAAAGGACAAAA | 55120 |
rs13032413 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207713 | AAGAGATCTTAAAGG[A/G]AAAAAAGAGTGATAA | 55120 |
rs13032432 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58198479 | agatttgggtatgca[C/T]ggattttggtattta | 55120 |
rs13032570 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58205776 | CTGGCAAAAATGCAG[C/T]GTTCAGGATAGAGAG | 55120 |
rs13032851 | snp | C/T | 0.194902 | 0.243853 | intron-variant | FANCL | GRCh38.p7 | 2:58168535 | tcatttgggcagaca[C/T]tgagctagctacagg | 55120 |
rs13383279 | snp | A/C | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58215393 | CCTCAATATCATAAT[A/C]TAGTACACTTACAAT | 55120 |
rs13385692 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58221246 | CTGGTGCTTTAGCTC[A/G]AAGTAGAAAGGTTAT | 55120 |
rs13394427 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | FANCL | GRCh38.p7 | 2:58211225 | ggttctgaaacctca[A/G]ttctggacttctgtg | 55120 |
rs13397947 | snp | C/G | 0.11963 | 0.213316 | intron-variant | FANCL | GRCh38.p7 | 2:58182072 | aagcattctgaatca[C/G]agaatctcaaatagg | 55120 |
rs13400272 | snp | C/T | 0.0722614 | 0.17581 | intron-variant | FANCL | GRCh38.p7 | 2:58239062 | actccttataatgaa[C/T]tgccacttcataaat | 55120 |
rs13404186 | snp | A/C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219273 | caatggccaaagcta[A/C/G]aacaaattgagcaag | 55120 |
rs13404519 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219547 | taactttacggtgca[A/G]aaacccgacaaatac | 55120 |
rs13404530 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219582 | tcaccaggtaatcaa[A/G]atcaagatcaacagt | 55120 |
rs13404538 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219588 | ggtaatcaagatcaa[A/G]atcaacagtgatgag | 55120 |
rs13404645 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58219651 | agaagaatCACAGGA[A/G]AACAAAAGTCAGGTA | 55120 |
rs13405745 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58207721 | TTAAAGGAAAAAAAG[A/G]GTGATAAACTCTTAC | 55120 |
rs13409706 | snp | A/C | 0.0399052 | 0.1355 | intron-variant | FANCL | GRCh38.p7 | 2:58178901 | tcaggatacaaaatc[A/C]atgtacaaaaatcac | 55120 |
rs13413755 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | FANCL | GRCh38.p7 | 2:58218058 | aaaatctccagttgt[C/T]tgaaaattaagagat | 55120 |
rs13417441 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58219173 | aaaaaaaaaaaaaaa[A/T]atatatatatatata | 55120 |
rs13417865 | snp | C/G | 0.115438 | 0.210697 | intron-variant | FANCL | GRCh38.p7 | 2:58168398 | GAGGGACTGTGCCAT[C/G]AGGAGTGGTGCACTC | 55120 |
rs13418724 | snp | A/G | 0.187685 | 0.242109 | intron-variant | FANCL | GRCh38.p7 | 2:58223398 | TAGTACTTCTTTCAA[A/G]ATTTGTTTTTATTCT | 55120 |
rs13421853 | snp | C/T | 0.118584 | 0.212673 | intron-variant | FANCL | GRCh38.p7 | 2:58190870 | CTAAAATTCAACTTT[C/T]ATTTTGGCACAAAAA | 55120 |
rs13422760 | snp | A/C | 0.296364 | 0.245663 | intron-variant | FANCL | GRCh38.p7 | 2:58217815 | aaaataaatcattaa[A/C]catattggatatctg | 55120 |
rs13424848 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | FANCL | GRCh38.p7 | 2:58200247 | CCATATTTAAAAATC[A/G]TGATTATCTCAAAGT | 55120 |
rs13428078 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | FANCL | GRCh38.p7 | 2:58170967 | tattagacagatcaa[A/C]gagacacaaaattaa | 55120 |
rs13431638 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58171935 | gacgggtttaaaaaa[C/T]ggcacaccaggagat | 55120 |
rs17049389 | snp | C/T | 0.0670745 | 0.170406 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161929 | TATATTGCTGTATTA[C/T]AGGAAATATAATTAC | 55120 |
rs17049394 | snp | A/G | 0.162909 | 0.23434 | intron-variant | FANCL | GRCh38.p7 | 2:58190682 | CATAAGTTCAAAACT[A/G]ATAGAAAGAATACCA | 55120 |
rs17049396 | snp | A/G | 0.11228 | 0.208646 | intron-variant | FANCL | GRCh38.p7 | 2:58191366 | TAGGACACCTGCTAT[A/G]TAAGAATATTTTACT | 55120 |
rs17049397 | snp | A/G | 0.0399052 | 0.1355 | intron-variant | FANCL | GRCh38.p7 | 2:58194411 | AAGCATTAAGGATAT[A/G]TTTTGAAGCATTTGT | 55120 |
rs17049402 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | FANCL | GRCh38.p7 | 2:58200620 | ACACAAAGTAAAGTA[C/T]CTGTGGCCCCATTAA | 55120 |
rs17049403 | snp | A/C | 0.139225 | 0.224118 | intron-variant | FANCL | GRCh38.p7 | 2:58200651 | GTACATACACAGCTC[A/C]TTATGCTAAAAGAGA | 55120 |
rs17049404 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58201606 | TAGTACTGATCTTGA[C/T]TGACCAAAGCTGAGG | 55120 |
rs17049406 | snp | A/T | 0.138546 | 0.223781 | intron-variant | FANCL | GRCh38.p7 | 2:58202735 | TATTAAATTGTCACA[A/T]CCTCACTCTGAATAC | 55120 |
rs17049407 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | FANCL | GRCh38.p7 | 2:58203439 | GACATCCTGGTTTTC[C/T]TCAAATTCTCATGTT | 55120 |
rs17049408 | snp | C/T | 0.138207 | 0.223612 | intron-variant | FANCL | GRCh38.p7 | 2:58203994 | TAAATTCTTTGAGGC[C/T]TTCCAAAATCAATGT | 55120 |
rs17049412 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | FANCL | GRCh38.p7 | 2:58204581 | TTCCTGTCAAACTCT[C/T]TGATCCATTTCTGTA | 55120 |
rs17049414 | snp | A/T | 0.0770498 | 0.180522 | intron-variant | FANCL | GRCh38.p7 | 2:58213034 | ACCAAATATGTAATT[A/T]AAAAACACAGCAAGG | 55120 |
rs17049416 | snp | C/G | 0.137867 | 0.223442 | intron-variant | FANCL | GRCh38.p7 | 2:58213866 | TTTTATTCGTGGTAA[C/G]ATACTTTTTATTAGT | 55120 |
rs17049417 | snp | A/G | 0.14933 | 0.228835 | intron-variant | FANCL | GRCh38.p7 | 2:58214407 | ACTCTCAAGAATCCT[A/G]TAATTATACTCTACC | 55120 |
rs17049420 | snp | C/T | 0.189261 | 0.242509 | intron-variant | FANCL | GRCh38.p7 | 2:58222703 | ACACATAAACATCAC[C/T]AGAATTGCTGAAGCT | 55120 |
rs17049422 | snp | C/T | 0.10237 | 0.201756 | intron-variant | FANCL | GRCh38.p7 | 2:58226925 | TAAGAAATGAAGTAT[C/T]GGTCATCAACTTTAC | 55120 |
rs17049423 | snp | C/T | 0.143284 | 0.226079 | intron-variant | FANCL | GRCh38.p7 | 2:58234768 | GAAAACAGAATATAA[C/T]TGGAAACAGACTTCT | 55120 |
rs17614782 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58215842 | ATTCCCTCAAAACTT[C/T]TGATAAATCCTTAAA | 55120 |
rs28364864 | in-del | -/TGGAAAAT | 0.314301 | 0.241589 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242094 | GGAAAATTGGAAAAT[-/TGGAAAAT]CAAATAATCATATGG | 55120 |
rs28391071 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197270 | CTATTAGGCTTTTTA[A/T]TTTTTTACTAATTTC | 55120 |
rs28391566 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | FANCL | GRCh38.p7 | 2:58226329 | ATGTAACAGTATACA[C/T]AAAATGAAGCCTAAT | 55120 |
rs28434419 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | FANCL | GRCh38.p7 | 2:58228074 | AACAATATGGTCATT[C/T]TTTTTATTTTTCCCT | 55120 |
rs28588526 | snp | C/T | 0.16028 | 0.233346 | intron-variant | FANCL | GRCh38.p7 | 2:58226450 | TAAACTCTCTGCTGA[C/T]AGGCCAGGAGTACAT | 55120 |
rs28631296 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58214680 | TTTATTTATTTATTT[A/T]TTTTTGTATTTTGTA | 55120 |
rs28645457 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58197269 | CCTATTAGGCTTTTT[A/T]TTTTTTTACTAATTT | 55120 |
rs28668929 | snp | A/G | 0.115438 | 0.210697 | intron-variant | FANCL | GRCh38.p7 | 2:58228699 | ATTAAAAATGATACA[A/G]GAAAAGAATAGTAAT | 55120 |
rs28833241 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58177642 | GTTGTGGGGTGGGGG[A/G]AGGGGGGAGGGATAG | 55120 |
rs28858137 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58177643 | TTGTGGGGTGGGGGG[A/G]GGGGGGAGGGATAGC | 55120 |
rs34038214 | in-del | -/G | | | utr-variant-3-prime, frameshift-variant, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159411 | AATGAAGTAAACAGT[-/G]TTCCCACAAAAAATC | 55120 |
rs34141328 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58233254 | GAAGAACTATTCTAT[-/C]ATAGAAATCTGTGCT | 55120 |
rs34333134 | in-del | -/A | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58190484 | GTACTATTCAAAAAG[-/A]AAAAAAAAAAAAAAA | 55120 |
rs34335951 | snp | A/G | 0.290718 | 0.246662 | intron-variant | FANCL | GRCh38.p7 | 2:58183226 | AAAATGAATAAAGAC[A/G]TAATTCCCTAAAAAG | 55120 |
rs34450901 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58232673 | GCCTCTAACTTTTTT[-/T]GAAATCAGTAACATA | 55120 |
rs34502821 | in-del | -/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188457 | TTTTTGGTTTTTTTT[-/T]GAGATAGGGTCTCTC | 55120 |
rs34553487 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58166885 | TCAGTTCCACTGTGC[-/C]TGGATTCAACTGTTC | 55120 |
rs34554148 | in-del | -/AAT/TAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58200871 | CAATATGTATATAAT[-/AAT/TAA]AAATTAGACTGATCT | 55120 |
rs34556232 | snp | C/T | 0.188 | 0.24219 | intron-variant | FANCL | GRCh38.p7 | 2:58238792 | CAACCTATTAAGGTG[C/T]ATAGTAAATTGACAT | 55120 |
rs34664107 | in-del | -/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243357 | GCTAATAAATTATTT[-/T]ACTAAATATCTTAAT | 55120 |
rs34683258 | snp | A/G | 0.0551013 | 0.156571 | intron-variant | FANCL | GRCh38.p7 | 2:58167256 | TAGAGCCTAATACCC[A/G]AAAAATAACCTTTGA | 55120 |
rs34723963 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58215257 | TTTGCTTGTCTTCCC[-/C]TGTCTCTCCTCACCA | 55120 |
rs34993644 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58183439 | CTTACAGCACTCCCC[-/C]TTATTAGTTACTGCT | 55120 |
rs35023213 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58234662 | TGATAAAAGTGATTC[A/C]CAATGATCAACTCTT | 55120 |
rs35156475 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58206191 | TGAATGGACGTGAAA[-/A]GAGGTTTAAGAAACA | 55120 |
rs35157712 | in-del | -/C | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160949 | TGTATCAACTAGGCC[-/C]TAAGGTGAAGCCAGG | 55120 |
rs35172654 | in-del | -/A | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58222316 | GAGATAAAAAAAAAA[-/A]TTTTTATTAAATTCA | 55120 |
rs35242386 | in-del | -/T | | | frameshift-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165765 | CTCCGTGGAGGTTTT[-/T]CTGGCTCAAGTACCC | 55120 |
rs35244714 | snp | C/G | 1.65589e-05 | 0.00287736 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162981 | AAATTATGCTGTGAA[C/G]TTTGTAAAATCACCA | 55120 |
rs35273533 | in-del | -/C | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243199 | ATGTTAAACTTCCCC[-/C]ACCACCACACTTTCC | 55120 |
rs35322153 | snp | C/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188198 | ATCTTTGTACCTTCG[C/T]TGAAAACAGCTGTCT | 55120 |
rs35341336 | snp | A/G | 0.134802 | 0.221877 | intron-variant | FANCL | GRCh38.p7 | 2:58212508 | ACAGGGGCCAAAACA[A/G]AAAGCATAAATTAGG | 55120 |
rs35360571 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58231743 | AAAGTTGGAAAAAAA[-/A]GTTTTCTAATCCTTT | 55120 |
rs35497921 | in-del | -/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241566 | GACTGACTGACCAAG[-/T]ATCATTCTAGCCTCA | 55120 |
rs35598830 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58193834 | CATGAAAAGAAAAAA[-/A]GGTTCACCATTTCCA | 55120 |
rs35631138 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58225431 | GATGATGGAATTTTT[-/T]AAAATTACCATTTGT | 55120 |
rs35646743 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58182541 | GGAATTTTTGAGGGG[-/G]TATACAATAAATTTG | 55120 |
rs35672834 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | FANCL | GRCh38.p7 | 2:58185402 | GTTTCTGAACACACA[C/T]ACTGAAAAGATTTCT | 55120 |
rs35691417 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58193776 | GGGGATTTGCCCCAA[-/A]CACTGTGTTTGTTTT | 55120 |
rs35698474 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58238655 | TAGGTCACAGGAAAA[-/A]GTACCAGTAAGTTCC | 55120 |
rs35706540 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58236968 | AATATATGAAGCAAA[-/T]ACTGATAGAAATTAA | 55120 |
rs35717987 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58212997 | TGTATAATGTCTAAT[-/T]CCTATAGAGTTGATT | 55120 |
rs35765242 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58192612 | TGAATATTATTATCC[-/C]AAATTACAATATAGT | 55120 |
rs35773188 | snp | A/T | 0.194278 | 0.243711 | intron-variant | FANCL | GRCh38.p7 | 2:58165355 | CCCAGATCTGAGCAC[A/T]CTAATCTGAGAAGAT | 55120 |
rs35818388 | in-del | -/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58184491 | AGCTTAAATACAGTG[-/G]AAGATCCAAAAATTA | 55120 |
rs35823028 | in-del | -/G | | | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162425 | ACGTCACTACTGAAG[-/G]ACCATGAAAAAAGTA | 55120 |
rs35908281 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58234756 | TCAAATATATAGAAA[-/C]ACAGAATATAATTGG | 55120 |
rs35925771 | snp | C/T | 0.192088 | 0.2432 | intron-variant | FANCL | GRCh38.p7 | 2:58210416 | CAATATGGGGGAAAC[C/T]GCCCTCCCACAACAC | 55120 |
rs35983748 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58219082 | GAAAAATGGCTGATT[C/T]TAGGAAAGGGCAGGA | 55120 |
rs36000054 | snp | A/G | 0.124491 | 0.216211 | intron-variant | FANCL | GRCh38.p7 | 2:58171719 | TCCATCTGAGGTACC[A/G]GGTTCATCTCACTAG | 55120 |
rs36059257 | snp | C/T | 0.0739645 | 0.177515 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204170 | AAGCAGAAGATGCTT[C/T]TGGTAGAGAGCATTT | 55120 |
rs36065368 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58205452 | TTCACCTCCAAAAAA[-/C]AATTAGAATGTCTTT | 55120 |
rs36079309 | in-del | -/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58205734 | AACAGAAAAGAAGAG[-/C]AGAACAAGGACTCCT | 55120 |
rs36101878 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58184574 | GTTTTGTGCATACAT[A/C]CAATAATAAGAATAA | 55120 |
rs36110008 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58204782 | CAATAAATTTTCTTT[-/T]CTGCACGATATATAG | 55120 |
rs41281511 | snp | C/G/T | 0.00476647 | 0.0486237 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241352 | GAAAAGCTCTAGACC[C/G/T]GCTGGGTCCTGCACA | 55120 |
rs55809167 | snp | G/T | 0.194278 | 0.243711 | intron-variant | FANCL | GRCh38.p7 | 2:58180812 | GTTTAAAGGTTTTTT[G/T]TGTGTGTGTGCCCAT | 55120 |
rs55849827 | snp | A/G | 0.00660771 | 0.0570981 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232097 | GCAACACTATCCTAA[A/G]GTGGAAGTCTCTTCC | 55120 |
rs56028716 | snp | C/G | 0.0988009 | 0.199095 | intron-variant | FANCL | GRCh38.p7 | 2:58172397 | CAGGTACTCCTCTGA[C/G]ACAAAACTTCCAGAG | 55120 |
rs56246409 | snp | A/G | 0.200492 | 0.245049 | intron-variant | FANCL | GRCh38.p7 | 2:58229620 | CAAAGATGGAAATCG[A/G]TTTCAACACAAAGGC | 55120 |
rs56387226 | in-del | -/TAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58200873 | ATATGTATATAATAA[-/TAA]ATTAGACTGATCTTT | 55120 |
rs56390816 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162076 | GTAATATTCCCATAT[C/G]ATACATTGTTATAAT | 55120 |
rs56730649 | snp | A/G | 0.384017 | 0.211044 | intron-variant | FANCL | GRCh38.p7 | 2:58239240 | CAAAAGGAGACTCTG[A/G]CAGATGATACCTTAA | 55120 |
rs57033851 | snp | A/G | 0.123452 | 0.215605 | intron-variant | FANCL | GRCh38.p7 | 2:58225278 | GCTAGGCACCAACTC[A/G]TTATTCTAAAAATTG | 55120 |
rs57267169 | snp | A/G | 0.276534 | 0.248588 | intron-variant | FANCL | GRCh38.p7 | 2:58169307 | TCCAGCAGACCTGCA[A/G]CAGAGGGGTCTGTTA | 55120 |
rs57334221 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58166986 | TGGGAGGCTGAGGTG[C/T]GCAGATCACGAGGTC | 55120 |
rs57344611 | snp | A/T | 0.150667 | 0.229419 | intron-variant | FANCL | GRCh38.p7 | 2:58201742 | TACTTCTACTTATTT[A/T]TTATTTACATATTTA | 55120 |
rs57442059 | snp | A/G | 0.0248432 | 0.108648 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243153 | AGCACTTTATAATTT[A/G]TCTGTGAATTAAGAT | 55120 |
rs57649910 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58185905 | TACTTGTACACTTAG[G/T]TCTAAACATTTTAAA | 55120 |
rs58059919 | snp | A/G | 0.149999 | 0.229128 | intron-variant | FANCL | GRCh38.p7 | 2:58225519 | AGGTGACAGTCTGAT[A/G]GGAAACTTTATATTG | 55120 |
rs58276647 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | FANCL | GRCh38.p7 | 2:58215981 | AGACAAAGTCTCAGT[A/G]AATACCCCAGGATCT | 55120 |
rs58321248 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58235202 | ACAGAGAAACGCCAG[C/T]GAATTTCAGAGGATT | 55120 |
rs58440082 | snp | A/C | 0.0475351 | 0.146656 | intron-variant | FANCL | GRCh38.p7 | 2:58202086 | GACAATCGCAGGCCC[A/C]ATTTCTTTTTTTTTC | 55120 |
rs58495080 | snp | A/T | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58210839 | TCCTTTGACTCCATG[A/T]CTCACATCCAGATCA | 55120 |
rs58756932 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | FANCL | GRCh38.p7 | 2:58187933 | TTTTAATTTTGATGA[C/T]GACCAATTTATCAAT | 55120 |
rs58950743 | snp | A/C | 0.0471551 | 0.14613 | intron-variant | FANCL | GRCh38.p7 | 2:58237028 | TGGAGATTTCAACAC[A/C]CCCTCTCACTAACTG | 55120 |
rs58973226 | snp | G/T | | | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188303 | ATCCTGAAAAAAGTA[G/T]ATTTTTAAGTCTTGA | 55120 |
rs59323329 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58184840 | AAAACGGGAGGAAAC[A/G]TCGTGAGAAAGTTAG | 55120 |
rs59964258 | in-del | -/TATATATATATATATACACACACACACACA | | | intron-variant | FANCL | GRCh38.p7 | 2:58217201 | ATATATATATATATA[lengthTooLong]CACACACACACACAT | 55120 |
rs60102555 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58166830 | AAAACCCATCCCATT[G/T]TGTCACTTCAGTCAA | 55120 |
rs60176808 | snp | C/G | 0.138546 | 0.223781 | intron-variant | FANCL | GRCh38.p7 | 2:58225089 | AGGCAAACAAGCTTG[C/G]GTTATATTAAATAAA | 55120 |
rs60381234 | in-del | -/A | 0.155656 | 0.231515 | intron-variant | FANCL | GRCh38.p7 | 2:58177792 | AGATTAAAAAAAAAA[-/A]GAAAAAGAAAAAACA | 55120 |
rs60949622 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58224479 | AAACTTTAGAAATTA[A/T]TTTTAAACTATTATT | 55120 |
rs60987670 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58223066 | TAGAAAGAACAGATA[C/T]TACAAAACAGCACTT | 55120 |
rs61361978 | in-del | -/TTTA | | | intron-variant | FANCL | GRCh38.p7 | 2:58220589 | ATGTTTAAGTCTCTA[-/TTTA]GTTTTTCTTTAGTTA | 55120 |
rs61405992 | snp | A/G | 0.138546 | 0.223781 | intron-variant | FANCL | GRCh38.p7 | 2:58179178 | TAATTTATAGATTCA[A/G]TGCTATCCCCATCAA | 55120 |
rs61582420 | in-del | -/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243325 | TCATTTAGCATATTT[-/T]CCTGCTGCATCGTAG | 55120 |
rs61753272 | snp | A/G | 0.00104783 | 0.0228651 | synonymous-codon, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163033 | AAGGTACCTACCACA[A/G]ATGTATGTTCCTGCT | 55120 |
rs61757387 | snp | A/C | | | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162909 | AAATCAATTTCTAAA[A/C]CATCTTTCAAATTTT | 55120 |
rs62140034 | snp | C/G | 0.108755 | 0.206276 | intron-variant | FANCL | GRCh38.p7 | 2:58171989 | CGCCCACGGAGCCTC[C/G]TTCATTGCTAGCACA | 55120 |
rs62140039 | snp | C/G | 0.0189856 | 0.0955633 | intron-variant | FANCL | GRCh38.p7 | 2:58192280 | AATCTTAGAAATCAA[C/G]TGAAACTATAGCGAT | 55120 |
rs62140040 | snp | C/T | 0.139564 | 0.224285 | intron-variant | FANCL | GRCh38.p7 | 2:58193922 | AATTAAATTAATGAC[C/T]GAATTGTAAACACAA | 55120 |
rs62140041 | snp | C/T | 0.100588 | 0.200439 | intron-variant | FANCL | GRCh38.p7 | 2:58194918 | ACAAAGCCATGTCTA[C/T]TATATCACAAAAAAA | 55120 |
rs62140042 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58200344 | CAAGTCATTTAATTT[C/T]TCTGGCTGTTTCACA | 55120 |
rs62140043 | snp | A/C | 0.138546 | 0.223781 | intron-variant | FANCL | GRCh38.p7 | 2:58202704 | AAGTATAGAAAAAAG[A/C]AGACAAAATGGACCA | 55120 |
rs62140044 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203407 | TGACTCCAAGAATAA[A/T]TAAAAAAAAAAAGTT | 55120 |
rs62140045 | snp | C/T | 0.138886 | 0.22395 | intron-variant | FANCL | GRCh38.p7 | 2:58204311 | AATTTGAAATGAAAA[C/T]ATTTGCTATATTCCT | 55120 |
rs62140046 | snp | C/T | 0.136847 | 0.222927 | intron-variant | FANCL | GRCh38.p7 | 2:58208181 | AGGAAACAATCATCA[C/T]TGGAAAGCTCAAATT | 55120 |
rs62140047 | snp | C/T | 0.138546 | 0.223781 | intron-variant | FANCL | GRCh38.p7 | 2:58216823 | GTGGGGTAGTTCTCC[C/T]TACCGCCCAGGTTGG | 55120 |
rs62140048 | snp | C/G | 0.117886 | 0.21224 | intron-variant | FANCL | GRCh38.p7 | 2:58220795 | ATTAAGAAAAACTTA[C/G]TGGTGAAAAATTGCA | 55120 |
rs62140049 | snp | A/G | 0.118933 | 0.212888 | intron-variant | FANCL | GRCh38.p7 | 2:58221106 | TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG | 55120 |
rs62140050 | snp | G/T | 0.118584 | 0.212673 | intron-variant | FANCL | GRCh38.p7 | 2:58221151 | CCGGGAGGCGGAGCT[G/T]GCAATCAGCCTAGGC | 55120 |
rs62140051 | snp | A/G | 0.118933 | 0.212888 | intron-variant | FANCL | GRCh38.p7 | 2:58224218 | GTTTAATGGGACATG[A/G]TATCTATACTTTTAC | 55120 |
rs62141871 | snp | C/T | 0.103438 | 0.202533 | intron-variant | FANCL | GRCh38.p7 | 2:58228064 | ATTATTAATTAACAA[C/T]ATGGTCATTTTTTTT | 55120 |
rs63678161 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58190484 | AAAAAAAAAAAAAAA[A/G]GGCCAAGCCAATTAG | 55120 |
rs67620550 | in-del | -/TAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58166164 | GCAATAGTAATGAGT[-/TAC]ACAAGATGTATGTAC | 55120 |
rs70954880 | in-del | -/TA | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58217216 | ATATATATATATATA[-/TA]CACACACACACACAC | 55120 |
rs70954881 | in-del | -/AA | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58219171 | AAAAAAAAAAAAAAA[-/AA]TATATATATATATAT | 55120 |
rs71394410 | in-del | -/TAC | 0.383053 | 0.211653 | intron-variant | FANCL | GRCh38.p7 | 2:58166163 | TGCAATAGTAATGAG[-/TAC]TACAAGATGTATGTA | 55120 |
rs71394412 | in-del | -/TAA | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58200870 | ACAATATGTATATAA[-/TAA]TAAATTAGACTGATC | 55120 |
rs71418483 | snp | A/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58168335 | TATCACCTCACTCAG[A/G]AAGCGCAAGGGGTTG | 55120 |
rs72536062 | in-del | -/TAC | | | intron-variant | FANCL | GRCh38.p7 | 2:58166165 | CAATAGTAATKASTA[-/TAC]CWASATGTATGTACA | 55120 |
rs72618693 | snp | C/T | 0.0260105 | 0.111035 | intron-variant | FANCL | GRCh38.p7 | 2:58194366 | CTCAGTCAAGAGTAT[C/T]TACACATCTGACCTG | 55120 |
rs72618694 | snp | C/T | 0.378372 | 0.214524 | intron-variant | FANCL | GRCh38.p7 | 2:58218775 | CTCGGTTTCTCCCTG[C/T]TGGAGTATGAGATTT | 55120 |
rs72618695 | snp | C/G | 0.378174 | 0.214642 | intron-variant | FANCL | GRCh38.p7 | 2:58235481 | AGCAATGCTTAAAAG[C/G]TTAAAGCTTAAAATT | 55120 |
rs72618696 | snp | C/T | 0.380919 | 0.21298 | intron-variant | FANCL | GRCh38.p7 | 2:58237892 | GAATGTGCATCTTTA[C/T]TGATCTCTCTGTTGT | 55120 |
rs72810360 | snp | C/T | 0.318174 | 0.240525 | intron-variant | FANCL | GRCh38.p7 | 2:58178580 | GTTGATGGAACATAT[C/T]TCAAAACAGTAACAG | 55120 |
rs72810363 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | FANCL | GRCh38.p7 | 2:58185904 | TTACTTGTACACTTA[A/G]GTCTAAACATTTTAA | 55120 |
rs72810367 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | FANCL | GRCh38.p7 | 2:58190393 | AAAGAAAGAAAGCTC[C/T]TCAAGCACATGCTGA | 55120 |
rs72810371 | snp | C/T | 0.146985 | 0.227789 | intron-variant | FANCL | GRCh38.p7 | 2:58193393 | CTTTCTCTTCTTTTT[C/T]AGAATCAATATAGGC | 55120 |
rs72810373 | snp | A/G | 0.300673 | 0.244811 | intron-variant | FANCL | GRCh38.p7 | 2:58199053 | AAAAAAAAGAAAAAC[A/G]AGATATATTGGGGGA | 55120 |
rs72810375 | snp | A/G | 0.148996 | 0.228688 | intron-variant | FANCL | GRCh38.p7 | 2:58201121 | ATAGTATTAACTACA[A/G]TGTAGATGACTAAAT | 55120 |
rs72810377 | snp | C/T | 0.138207 | 0.223612 | intron-variant | FANCL | GRCh38.p7 | 2:58201143 | TGACTAAATACAATA[C/T]AAGAAAGTAACTTGA | 55120 |
rs72810378 | snp | A/G | 0.138207 | 0.223612 | intron-variant | FANCL | GRCh38.p7 | 2:58201183 | AGATACTTTTCAATA[A/G]TAAGTTGTATAGGTA | 55120 |
rs72810385 | snp | C/T | 0.147656 | 0.228091 | intron-variant | FANCL | GRCh38.p7 | 2:58218394 | AATTGATATGGCTCT[C/T]GCAAAACTGATTAAG | 55120 |
rs72810393 | snp | C/G | 0.145978 | 0.227331 | intron-variant | FANCL | GRCh38.p7 | 2:58227456 | GTGGGAGACAGAAGG[C/G]AGACGGTTTTCCCCT | 55120 |
rs72810394 | snp | A/G | 0.145642 | 0.227177 | intron-variant | FANCL | GRCh38.p7 | 2:58227974 | GAGTGATGTGAGTGG[A/G]AAGAGGAGTATAAAA | 55120 |
rs72810396 | snp | C/T | 0.189261 | 0.242509 | intron-variant | FANCL | GRCh38.p7 | 2:58228837 | TTGATAACTTGCTGG[C/T]GAAAAACAGAGTAAT | 55120 |
rs72812352 | snp | A/T | 0.135143 | 0.222054 | intron-variant | FANCL | GRCh38.p7 | 2:58236545 | AGAATTCCAATAATA[A/T]AAAATACAGAAAAAT | 55120 |
rs72812353 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58238183 | TTTTTTTTAGCTTAT[C/T]AGCTATCATTAGTGT | 55120 |
rs72812354 | snp | C/G | 0.0345262 | 0.126772 | intron-variant | FANCL | GRCh38.p7 | 2:58240170 | AAATGTTGTCTACAA[C/G]AGAATCATATTTTCA | 55120 |
rs72812356 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242193 | CAAAGATTATTTCGT[C/T]CCCTACCCATCTTTA | 55120 |
rs72812357 | snp | C/T | 0.312837 | 0.241974 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242747 | TTCTTTGGGCTTCAT[C/T]TCTGAAGGCTCCCAT | 55120 |
rs72948815 | snp | A/G | 0.0486741 | 0.148216 | intron-variant, downstream-variant-500B, stop-lost, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160050 | ATAGATCTATCTTCT[A/G]GAACATATTACTGAA | 55120 |
rs72948818 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58166269 | GTATGAAAATCTTAA[C/T]TTCATGTTTGCTGCA | 55120 |
rs72948825 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58171974 | GCTTGGAGAGTCCTA[C/T]GCCCACGGAGCCTCC | 55120 |
rs72948841 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FANCL | GRCh38.p7 | 2:58184555 | TCAAAGCAAAATGCC[A/G]TCTGTTTTGTGCATA | 55120 |
rs72948853 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FANCL | GRCh38.p7 | 2:58193884 | GAGGCAAAGGGCAGT[C/T]ATGTGACTTGTCTGA | 55120 |
rs72948858 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | FANCL | GRCh38.p7 | 2:58197228 | TAATTAAAATGGCAT[C/T]TTGGCCTTGACAAGA | 55120 |
rs72948859 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FANCL | GRCh38.p7 | 2:58197433 | TGTTTTTTCTCTTTG[C/T]CTAAGAATAAAAATG | 55120 |
rs72948860 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58203391 | AAAAGAGTTGATTGA[C/T]TGACTCCAAGAATAA | 55120 |
rs72948861 | snp | G/T | 0.0471551 | 0.14613 | intron-variant | FANCL | GRCh38.p7 | 2:58207588 | CTTGTTTCAACTACT[G/T]AGGATTTACATTTCT | 55120 |
rs72948864 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FANCL | GRCh38.p7 | 2:58208597 | TTTAGCCATCTAGAT[A/G]CATTTAAGTAGTATT | 55120 |
rs72948870 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58215478 | TTCTACAGTGAACAA[C/G]TAAAGTAGGCTGATA | 55120 |
rs72948876 | snp | C/T | 0.12932 | 0.218944 | intron-variant | FANCL | GRCh38.p7 | 2:58217448 | AACTATGAAAGAAAA[C/T]AGAGAAAAAGAGGAA | 55120 |
rs72948884 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58223999 | TGAGCAATAAAATCA[C/T]CAAATTTGTCCGTAA | 55120 |
rs72948885 | snp | C/G | 0.0482946 | 0.147699 | intron-variant | FANCL | GRCh38.p7 | 2:58225973 | ATAAGAAATTATTAA[C/G]TTTATTGAGGTTATA | 55120 |
rs72948886 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58227655 | TATTTCTCTCAACGT[C/T]CAGCCACTTGTGTGT | 55120 |
rs72948887 | snp | C/G | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58227790 | AGGCCCGGGGGTGGA[C/G]CCCTCACCAGGGACC | 55120 |
rs72948894 | snp | C/G/T | 0.00836003 | 0.0642105 | intron-variant | FANCL | GRCh38.p7 | 2:58238442 | AGCAGCAAAAGATAA[C/G/T]CAACATAGAGAGCAT | 55120 |
rs72948895 | snp | A/C/G | 0.0591596 | 0.162834 | intron-variant | FANCL | GRCh38.p7 | 2:58238974 | ATAAATAATGATTAT[A/C/G]ATCAAGTAATTTTTT | 55120 |
rs72948898 | snp | A/G | 0.046775 | 0.145601 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242659 | AGTTTATTACCATTA[A/G]ACCATGCTTTGTCCA | 55120 |
rs72948900 | snp | C/G | 0.046775 | 0.145601 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243030 | TTTATTTTGCAACTC[C/G]GTAATTAAGGACGGC | 55120 |
rs73944826 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58178220 | GAAAAATGACTCCTC[C/T]CTAACTCATTTTATG | 55120 |
rs73944827 | snp | G/T | 0.0509478 | 0.151255 | intron-variant | FANCL | GRCh38.p7 | 2:58182556 | GTATACAATAAATTT[G/T]TAAGAAATAAAACCC | 55120 |
rs73944828 | snp | A/G | 0.0629771 | 0.165899 | intron-variant | FANCL | GRCh38.p7 | 2:58183149 | GGACAAAGGATTGAT[A/G]CCCTTAATATATATA | 55120 |
rs73944829 | snp | C/T | 0.0670745 | 0.170406 | intron-variant | FANCL | GRCh38.p7 | 2:58185294 | CTTAATGAAATTCTC[C/T]GCACCTAAATCAGAA | 55120 |
rs73944832 | snp | A/G | 0.490782 | 0.0672626 | intron-variant | FANCL | GRCh38.p7 | 2:58190468 | TGTACTATTCAAAAA[A/G]AAAAAAAAAAAAAAA | 55120 |
rs73944834 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FANCL | GRCh38.p7 | 2:58194131 | TCCATGATAAAAAAA[C/T]ATAAAGACCACTATT | 55120 |
rs73944835 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58200185 | AAATATCAGATGATG[C/T]GCTTCAGAGTATCAT | 55120 |
rs73944837 | snp | C/G | 0.0509478 | 0.151255 | intron-variant | FANCL | GRCh38.p7 | 2:58216163 | ATATACCTGGCTCTT[C/G]CTTGGAAGCTCTAAA | 55120 |
rs73944838 | snp | C/T | 0.0513262 | 0.151752 | intron-variant | FANCL | GRCh38.p7 | 2:58222164 | GTGCCTGTTTTTTTA[C/T]GGAAATCTGGCTGAC | 55120 |
rs73944839 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58225029 | ATGGCTGATTACAGT[C/T]ACGGAATAAAATGAA | 55120 |
rs73944840 | snp | A/G | 0.0505692 | 0.150756 | intron-variant | FANCL | GRCh38.p7 | 2:58226460 | GCTGATAGGCCAGGA[A/G]TACATTTTATTTCTT | 55120 |
rs74480045 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240797 | CCAAATGTTCTTTCT[A/G]CAGGAAACACGAAAA | 55120 |
rs74561078 | snp | A/T | 0.0441095 | 0.141807 | intron-variant | FANCL | GRCh38.p7 | 2:58164722 | CGAAAATAATGATTT[A/T]CTACATTTCTTTGAA | 55120 |
rs74749607 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FANCL | GRCh38.p7 | 2:58189614 | GAAAGCACTTAAGCA[A/G]GAAAGTATGAACACT | 55120 |
rs74778101 | snp | C/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58170352 | GAGAGATTTTGTCAC[C/G]ACCAGGCCTGCCCTA | 55120 |
rs74832762 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58163938 | CAAATGTAAAAAGAC[C/T]AACAATACAGTAAAT | 55120 |
rs74924593 | snp | A/C | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58236051 | CAGAAAAGGAGGAAC[A/C]AAAAAAAAAAAAGAA | 55120 |
rs75004186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235203 | CAGAGAAACGCCAGC[A/G]AATTTCAGAGGATTC | 55120 |
rs75008154 | snp | A/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58240128 | AAAAAAAAAAAAAAA[A/G]GTAACTTAAAATTTT | 55120 |
rs75077933 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58195719 | GGAAAAAAATATAGG[C/T]TAAGGCTATGGACAC | 55120 |
rs75082617 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | FANCL | GRCh38.p7 | 2:58166858 | CAAGGTTTACACTTG[A/G]ATGAATTCATGCTCA | 55120 |
rs75144070 | snp | A/C/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58171754 | ACACACACTGGCCTG[A/C/T]GCCCACTGTCTGGCA | 55120 |
rs75205222 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | FANCL | GRCh38.p7 | 2:58181346 | TATCTGGAATAGACA[C/T]AACTAAGCTTTGGTG | 55120 |
rs75241352 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | FANCL | GRCh38.p7 | 2:58236314 | TAGAAAACAGTGCAA[A/G]ACAGTGAAGTAACAT | 55120 |
rs75262215 | snp | C/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58171841 | TTTGACTAGGAAAGA[C/G]AACTCCCTGACCCTT | 55120 |
rs75268528 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | FANCL | GRCh38.p7 | 2:58167734 | CATTATACGATTTTA[A/C]TAGCTAGCCATTTGA | 55120 |
rs75366675 | snp | G/T | 0.0475351 | 0.146656 | intron-variant | FANCL | GRCh38.p7 | 2:58213859 | TCGTCCATTTTATTC[G/T]TGGTAAGATACTTTT | 55120 |
rs75374007 | snp | G/T | 0.039522 | 0.134904 | intron-variant | FANCL | GRCh38.p7 | 2:58184481 | AACAACTGTACAGCT[G/T]AAATACAGTGAAGAT | 55120 |
rs75534727 | in-del | -/A | 0.380529 | 0.213219 | intron-variant | FANCL | GRCh38.p7 | 2:58206504 | TAAGAGGGGTGGAAG[-/A]AAAAAACTACATCAC | 55120 |
rs75713133 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58203643 | CCTCTGCAAATTCTT[A/G]AAATACTTAAAAAAC | 55120 |
rs75781229 | in-del | -/AA | | | intron-variant | FANCL | GRCh38.p7 | 2:58187579 | ATAATAAAAAAAAAA[-/AA]GTGTTGCAAAGAAAG | 55120 |
rs75902380 | snp | A/C | 0.114036 | 0.209795 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162677 | CCCTGAAATCAATCC[A/C]CCTGTTCCAAGAGAC | 55120 |
rs75970912 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58222598 | ATGCCATCCATCTGG[A/C]TAGATTACAGTCCCG | 55120 |
rs76013817 | snp | C/T | 0.151001 | 0.229563 | intron-variant | FANCL | GRCh38.p7 | 2:58170277 | TAGAATTTCCTATCC[C/T]GCCAAACTAACCTTC | 55120 |
rs76023686 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58223101 | ACCAAAACTATTAAC[C/G]GGAACTACTTCAATT | 55120 |
rs76102266 | snp | G/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58240129 | AAAAAAAAAAAAAAA[G/T]TAACTTAAAATTTTT | 55120 |
rs76190239 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | FANCL | GRCh38.p7 | 2:58191765 | CTTCTTTGCCCATAT[G/T]AGCTCTCACTATATT | 55120 |
rs76305302 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | FANCL | GRCh38.p7 | 2:58230597 | TACTTTTAGTTACCT[A/G]CAAGTAGGAAGCCTC | 55120 |
rs76348639 | snp | C/T | 0.00478431 | 0.0486751 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159670 | CTTTTGATGTTAGTA[C/T]TTCTTGCTTTATTTT | 55120 |
rs76526191 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242283 | ACAGCATTCTGGATG[C/G]TTACAGAAAAGAATG | 55120 |
rs76540117 | snp | A/C | 0.0543475 | 0.155628 | intron-variant | FANCL | GRCh38.p7 | 2:58217927 | GAAATAGAACACATA[A/C]CAAAATTGACAAGGT | 55120 |
rs76615558 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188350 | TCTTCTAACTTTTTT[C/T]CTTTTTCAGAGTTAT | 55120 |
rs76708228 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | FANCL | GRCh38.p7 | 2:58236475 | TAGTTAAAAAAAAAA[A/C]ACACACACACACAGC | 55120 |
rs76826456 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58200654 | CATACACAGCTCATT[A/T]TGCTAAAAGAGAGTA | 55120 |
rs76883767 | snp | C/T | 0.0644693 | 0.167566 | intron-variant | FANCL | GRCh38.p7 | 2:58219428 | CCAAATCTGTGTAAA[C/T]ACTGTGCCCTAAAGG | 55120 |
rs76887336 | snp | A/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58240130 | AAAAAAAAAAAAAAG[A/T]AACTTAAAATTTTTC | 55120 |
rs76889506 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58196620 | AAATTTAAAAGAAAT[C/T]GCCTTCAAAGACTTT | 55120 |
rs77062954 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | FANCL | GRCh38.p7 | 2:58181018 | GACAATTTCTTTAAG[A/G]ACTAAATATATTCCT | 55120 |
rs77160702 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58219413 | CTGAGCAGAAAAATT[A/C]CAAATCTGTGTAAAT | 55120 |
rs77228196 | snp | C/G/T | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58234639 | ACCAAAAGGGATAAG[C/G/T]GGCCACATGATAAAA | 55120 |
rs77274446 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58218347 | GAGAAAATTAACAAC[A/G]CTAAAAGTTGGGTCT | 55120 |
rs77287711 | snp | A/G | 0.0770498 | 0.180522 | intron-variant | FANCL | GRCh38.p7 | 2:58207771 | TGTCTAAGGAAGTCT[A/G]TTTCATGTCGGGCAT | 55120 |
rs77365946 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | FANCL | GRCh38.p7 | 2:58199539 | AATAAAACAGTTTTT[A/G]GCAAGAAAAACCTTT | 55120 |
rs77408131 | in-del | -/AA | 0.0785177 | 0.181917 | intron-variant | FANCL | GRCh38.p7 | 2:58230136 | TAACACATCCGAAGC[-/AA]AGTTTTCCACTGAAG | 55120 |
rs77467661 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FANCL | GRCh38.p7 | 2:58224789 | AACATTAGAAAACAG[C/G]ATTTTCAGAGTAAAA | 55120 |
rs77524104 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | FANCL | GRCh38.p7 | 2:58181751 | AATGTTTCTTGTATG[C/T]CAGAAAATTTGTAAT | 55120 |
rs77548893 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58208051 | GTGAAAGACAGAGAC[C/G]ATGTCACTAAATTTT | 55120 |
rs77566986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58240379 | CAGAAAGGAAAAGTC[C/T]ACACTCCTAACCTAA | 55120 |
rs77679102 | snp | C/T | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58177920 | GATATCGCCACTGAT[C/T]CTACAGAAATACAAA | 55120 |
rs77799330 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58213558 | AAATGATTAAGTAAC[A/G]GCAGCTAAATCGAAA | 55120 |
rs77807900 | snp | A/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58171784 | CAGCGCACCGTGCGC[A/G]AGCCGAAGCAGGACG | 55120 |
rs77949670 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58183079 | AGACATATAGTACTC[A/G]TCCTAGAGAAGTTCA | 55120 |
rs78016648 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58231376 | TTCACACCAAATATG[C/G]CTTAAAACAATCTCT | 55120 |
rs78035081 | snp | C/T | 0.102014 | 0.201495 | intron-variant | FANCL | GRCh38.p7 | 2:58182941 | AGCAAGTTACTTACC[C/T]CCCTTAGCATTTGTA | 55120 |
rs78166507 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58241003 | AGCCCCGCTCCACGC[C/T]GCGCGCCTCCTCGCT | 55120 |
rs78217793 | snp | G/T | 0.375 | 0.216506 | intron-variant | FANCL | GRCh38.p7 | 2:58169388 | TGACCTTTGGATGGG[G/T]TTTTTATGTGGGTGT | 55120 |
rs78289580 | snp | G/T | 0.0685596 | 0.171987 | intron-variant | FANCL | GRCh38.p7 | 2:58206498 | GCACGTTTAAGAGGG[G/T]TGGAAGAAAAAACTA | 55120 |
rs78612128 | in-del | -/AA | | | intron-variant | FANCL | GRCh38.p7 | 2:58188782 | AAGGAAAAAAAAAAA[-/AA]GAGCTGTTGGGATTT | 55120 |
rs78694832 | snp | A/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58203040 | TTAAAAAAAAAAAAA[A/G]AGCACACTTTTACAA | 55120 |
rs78712802 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58206509 | GGGGTGGAARAAAAA[-/A]ACTACATCACCACCT | 55120 |
rs78744369 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58233850 | GGAAAGAATGCTTTA[A/G]AGGCAGAAGATAGGA | 55120 |
rs78792921 | in-del | -/TAAT | | | intron-variant | FANCL | GRCh38.p7 | 2:58204345 | ATCCATTATAAAAAT[-/TAAT]CAGAGCAATTTCTGC | 55120 |
rs78812734 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | FANCL | GRCh38.p7 | 2:58197374 | TTTTATAGCCAAAAT[C/G]AGTAGCCTCCATTTA | 55120 |
rs78881378 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FANCL | GRCh38.p7 | 2:58228889 | TAAACCATTTTTTCC[C/T]ATGCTATTTCAATAT | 55120 |
rs79031739 | in-del | -/AAA | | | intron-variant | FANCL | GRCh38.p7 | 2:58240126 | AAAAAAAAAAAAAAA[-/AAA]GTAACTTAAAATTTT | 55120 |
rs79064653 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | FANCL | GRCh38.p7 | 2:58225396 | AAGTTCTCTACAGAA[A/G]ATTTTCAACTAATAA | 55120 |
rs79123434 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236991 | GAAATTAAATAGAAA[C/T]TGAAAAATCAACAAA | 55120 |
rs79147905 | snp | A/G | 0.0626037 | 0.165477 | intron-variant | FANCL | GRCh38.p7 | 2:58177765 | GTGCACATGTACACT[A/G]AAACTTAATAATAAA | 55120 |
rs79268223 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | FANCL | GRCh38.p7 | 2:58240075 | AGACATACATAACAG[C/T]ATTTTGCCTAAAATT | 55120 |
rs79405536 | snp | A/T | 0.0818113 | 0.184966 | intron-variant | FANCL | GRCh38.p7 | 2:58214140 | TGGCACACAACAGAA[A/T]CTTCATAAACAACAG | 55120 |
rs79442003 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | FANCL | GRCh38.p7 | 2:58183827 | AACATTTTAGCCATG[C/T]ACAGGACTACGTTGG | 55120 |
rs79546443 | snp | A/C | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58236474 | CTAGTTAAAAAAAAA[A/C]CACACACACACACAG | 55120 |
rs79572158 | snp | C/T | 0.193653 | 0.243567 | intron-variant | FANCL | GRCh38.p7 | 2:58231142 | TAGTCTCCTTGTAAG[C/T]TCCTCTTTAGTGACC | 55120 |
rs79578884 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | FANCL | GRCh38.p7 | 2:58174785 | GCAAGAAATAACTAA[A/C]ACCAGAGCAGAACTG | 55120 |
rs79588315 | snp | A/G | 0.132876 | 0.220866 | intron-variant | FANCL | GRCh38.p7 | 2:58226795 | ATTCTCTAGATCAAA[A/G]TATTTCCAATTAATT | 55120 |
rs79695454 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58187726 | TAAATTTATATAAAG[C/T]TTTAATGGTAGTAAA | 55120 |
rs79696245 | snp | C/G | 0.0345262 | 0.126772 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188359 | TTTTTTTCTTTTTCA[C/G]AGTTATTTTAACTAT | 55120 |
rs79724076 | snp | C/T | 0.0633504 | 0.166319 | intron-variant | FANCL | GRCh38.p7 | 2:58214094 | TCCTGAGAAATTAAA[C/T]AAGAATACATGAAGC | 55120 |
rs79791335 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58227999 | ATAAAATATAAAAAT[C/T]AGGCAACTCTATGTA | 55120 |
rs79887952 | snp | C/T | 0.0333695 | 0.124785 | intron-variant | FANCL | GRCh38.p7 | 2:58185636 | ATGAGTCAAAGACCC[C/T]GATAATTAAGCAGGG | 55120 |
rs80099621 | snp | A/G | 0.0839998 | 0.186933 | intron-variant | FANCL | GRCh38.p7 | 2:58235134 | ACAATTGTACAATTC[A/G]CAAGGTATAGTACCA | 55120 |
rs80184716 | snp | A/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58233748 | AAGTGTAAAAAAAAA[A/T]AGTAACAAGCTCTGG | 55120 |
rs80193830 | snp | C/G | 0.0379877 | 0.132479 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163379 | AATAATTTAACAATG[C/G]TAGGCAAGGATTTTA | 55120 |
rs80225324 | snp | A/G | 0.197393 | 0.244402 | intron-variant | FANCL | GRCh38.p7 | 2:58179405 | TAGACCAATGGAACA[A/G]AACAGAGGCCTCAGA | 55120 |
rs80298100 | snp | G/T | 0.0283406 | 0.115616 | intron-variant | FANCL | GRCh38.p7 | 2:58184489 | TACAGCTTAAATACA[G/T]TGAAGATCCAAAAAT | 55120 |
rs111232204 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161801 | ATTTACCTTTTATGT[C/T]GGGAACATTACAATT | 55120 |
rs111237370 | snp | G/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58170222 | CCAGAAGAGAGTGGG[G/T]GCCAATATTTAATAT | 55120 |
rs111310548 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58217205 | ATATATATATATATA[G/T]ATATATATATACACA | 55120 |
rs111310815 | snp | C/G | 0.0475351 | 0.146656 | intron-variant | FANCL | GRCh38.p7 | 2:58180557 | CACCAGGGCCTGTCG[C/G]GGGGTGGGGGACTAG | 55120 |
rs111387910 | in-del | -/G | 0.391583 | 0.206044 | intron-variant | FANCL | GRCh38.p7 | 2:58213735 | AAAAAAAAAAAGAGA[-/G]GGGAAAAAAAGTCAT | 55120 |
rs111400252 | snp | A/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58166168 | ATAGTAATGAGTACA[A/T]GATGTATGTACACAC | 55120 |
rs111423047 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58204372 | CTGCATGCCAACCCT[C/T]TCTGCTGCTATAGAT | 55120 |
rs111441322 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58168562 | CAGGAGTTTTTTTTT[A/T]AATACCCCAGTGGCG | 55120 |
rs111443214 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58203486 | GGTAAATGATTAATA[G/T]GCTAAACTTGTTTAT | 55120 |
rs111464169 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58213302 | GCAATTCTAGTATGT[A/G]GACAGCACAGTTCAG | 55120 |
rs111571239 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58165583 | ACATTTAAATGTGTA[A/G]CCAAAAAAAAGTTTA | 55120 |
rs111756132 | snp | A/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58230068 | TTATTTCAAAATATA[A/G]ATAACTGCAATCAGT | 55120 |
rs111842758 | snp | C/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161374 | AATGAAGCACATAAG[C/G]ATCTGGAATAAACTG | 55120 |
rs111863996 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58238619 | TGATAATAGAGACAA[C/T]ACCTAAAACTGATTA | 55120 |
rs112032953 | snp | C/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58217464 | AGAGAAAAAGAGGAA[C/G]AATTTCAATACAGCA | 55120 |
rs112072929 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58228829 | GAATCCTCTTGATAA[C/T]TTGCTGGTGAAAAAC | 55120 |
rs112075853 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58231974 | GCAAAACTCTAGTCA[C/T]TAGAATCAATTTATA | 55120 |
rs112101932 | snp | A/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58200146 | GCTGAAATTAAAAGA[A/G]GAAGTTCTATTTCAG | 55120 |
rs112109001 | snp | A/G | 0.089084 | 0.191327 | intron-variant | FANCL | GRCh38.p7 | 2:58177821 | AAAGAAAAAACAAAA[A/G]AAACCCAAATAGACC | 55120 |
rs112116596 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58212004 | ACCCAGTTCCAAAGT[C/T]GCTTCCACATTTTCA | 55120 |
rs112144223 | snp | C/T | 0.030278 | 0.119257 | intron-variant | FANCL | GRCh38.p7 | 2:58227812 | CCAGGGACCCATCTT[C/T]CTCTACTCAGCACTT | 55120 |
rs112156290 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188591 | ACTACAGACACGTTG[C/G]CCCCACACCCAGCTG | 55120 |
rs112187740 | snp | C/T | 0.136847 | 0.222927 | intron-variant | FANCL | GRCh38.p7 | 2:58221137 | GGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG | 55120 |
rs112229739 | in-del | -/A | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58218619 | GAAGCCTATAAAGGC[-/A]AAAAAAAAAAAACTA | 55120 |
rs112234416 | snp | A/G | 0.299664 | 0.245017 | intron-variant | FANCL | GRCh38.p7 | 2:58212088 | TGTTTTCATGCTGCT[A/G]ATAAAGACATACCCA | 55120 |
rs112301635 | snp | A/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58239748 | CCTCAAATGGTTCAG[A/G]AAAATAATGTGTATA | 55120 |
rs112309259 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58168862 | GCAGAGCTCACCGCA[C/G]CTCAGCAAAGCCTCT | 55120 |
rs112329607 | snp | A/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58169477 | AAGGAGGAAAATTCC[A/G]AAAACCAGAACACCT | 55120 |
rs112551221 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58168273 | CTCATTGGGACTGGT[C/T]AGATAGTGGGTGCAG | 55120 |
rs112566764 | in-del | -/A | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58190211 | ACCTCTTCTATACTT[-/A]AAGTTATTTTGACTA | 55120 |
rs112604126 | in-del | -/A | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58216129 | AGTTTAGGATCTACC[-/A]GGGGGGAAATCCCAA | 55120 |
rs112606329 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58180280 | GCATACATATGTTTA[C/T]TCCAGCATTATTCAC | 55120 |
rs112609502 | snp | A/G | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58197884 | TCAAAAGTTTTAGCA[A/G]TATAAAACATTTCAC | 55120 |
rs112644562 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58186300 | GTAAATTTCTGGGCC[A/G]TAAGTATGATTGGTA | 55120 |
rs112682398 | snp | C/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58193435 | TAAATAATTAGCTAT[C/T]GAGAAAGAAAAATAA | 55120 |
rs112696114 | snp | A/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58216520 | ACCAGTTCTTTTGAA[A/G]GAAAGAATAGTTACC | 55120 |
rs112724482 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58173468 | CAAGCCAGAAGAGAG[C/T]GGGAGCCAATATTCA | 55120 |
rs112778976 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58169269 | CCCAGGCAAACAAGG[C/T]CTGGAGTGGACCTCC | 55120 |
rs112879470 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58229484 | TTTGCCACAGATATC[C/T]CACAGCTCTAAATGG | 55120 |
rs112994651 | snp | A/G | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58232005 | CCAAATGTACTGCCT[A/G]TCCCACCAAAATGCA | 55120 |
rs113273275 | snp | A/G | 0.320335 | 0.239902 | intron-variant | FANCL | GRCh38.p7 | 2:58178874 | AAGCTGATAAGCAAC[A/G]TCAGCAAGGTCTCAG | 55120 |
rs113315535 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58222851 | TACAAAAAGTAAATA[A/G]TTAATTAATTAAATA | 55120 |
rs113379952 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58240999 | CCCCAGCCCCGCTCC[A/G]CGCCGCGCGCCTCCT | 55120 |
rs113438899 | snp | C/T | 0.0471551 | 0.14613 | intron-variant | FANCL | GRCh38.p7 | 2:58212100 | GCTGATAAAGACATA[C/T]CCAAGATTGGGCAAT | 55120 |
rs113480493 | in-del | -/GT/GTGT | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58198028 | TCTACAGGCTGGATG[-/GT/GTGT]GTGTGTGTGTGTGTG | 55120 |
rs113490416 | snp | G/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58233211 | AAGGTGTAAGAACAA[G/T]TTGGAATTCTTAATT | 55120 |
rs113506246 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58181414 | ACAAAACCCTGTGAT[A/G]TTAATAATGTTCTGC | 55120 |
rs113506287 | snp | C/T | 0.0825414 | 0.185628 | intron-variant | FANCL | GRCh38.p7 | 2:58211263 | AGGCTCAACAACATG[C/T]GGAAGCTGCCAAGGC | 55120 |
rs113577613 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58170052 | ACCACAAAGATACTC[C/G]TCCAGAACAGCAACC | 55120 |
rs113782435 | snp | A/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58166167 | AATAGTAATGAGTAC[A/T]AGATGTATGTACACA | 55120 |
rs113884099 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | FANCL | GRCh38.p7 | 2:58234716 | TTTCAAAATAAGAAA[A/G]AAGTCCAGAGTCTCT | 55120 |
rs113922373 | in-del | -/AAAT | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58194505 | ATTAACTGAGCAAAC[-/AAAT]AAAGCAAATATCTAG | 55120 |
rs113982347 | snp | C/T | 0.5 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58193500 | GTCAAATGACTGCTA[C/T]GCTTATACTTTTTCT | 55120 |
rs113983570 | snp | A/G | 1.81269e-05 | 0.00301051 | utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241334 | GAAGTCCGGAGAAAC[A/G]CAGAAAAGCTCTAGA | 55120 |
rs113998559 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | FANCL | GRCh38.p7 | 2:58185146 | CTAATCTTCCTATGG[C/T]GAAAAATCAAAGGTC | 55120 |
rs114057378 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58233562 | ACCACAAAAATCCCA[A/T]GTTTTCAGCCAGAAG | 55120 |
rs114109135 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58199321 | GATCAAATGAGTTGA[A/T]ATTTAATTTTCTTCT | 55120 |
rs114128639 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58218318 | AGATATTAATGATAA[A/T]AAAATATACAACAGA | 55120 |
rs114236282 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | FANCL | GRCh38.p7 | 2:58224524 | TTAATCAAAGTCCTA[A/C]CTTAGAAGGTTCTTA | 55120 |
rs114254283 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58182420 | AGAGTCACACTTCCA[C/T]ACAATTCACAAAAAG | 55120 |
rs114317045 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | FANCL | GRCh38.p7 | 2:58231184 | TGTTGGTACGCCCCA[A/G]GGTCTTGTCACTGGC | 55120 |
rs114331129 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58216144 | AGGGGGGAAATCCCA[A/G]TGAATATACCTGGCT | 55120 |
rs114472370 | snp | A/G | 0.0107246 | 0.0724382 | | | GRCh38.p7 | 2:58243587 | GTGTGACCACTTGCC[A/G]AAAGCAGTTGGCTCC | 55120 |
rs114568223 | snp | C/T | 0.0252325 | 0.109451 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241864 | GCACACACATGTATA[C/T]GTATATGTGTATTGA | 55120 |
rs114576415 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | FANCL | GRCh38.p7 | 2:58216850 | TTGGAATCCAAGCAC[A/G]GGGGTAAAGCGGGTG | 55120 |
rs114581395 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FANCL | GRCh38.p7 | 2:58166231 | CTAACATTGGACCTA[C/T]ACAAAATGTCTATAA | 55120 |
rs114629764 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | FANCL | GRCh38.p7 | 2:58169405 | CCATATGAAAGTCAA[A/C]AATATCAAAGACCAA | 55120 |
rs114680290 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | FANCL | GRCh38.p7 | 2:58197304 | TATATTTACTTTACT[C/T]ATGTATTTATGTTTT | 55120 |
rs114766239 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FANCL | GRCh38.p7 | 2:58207475 | GAGAAACAAAAGAAA[C/T]CTGGATTCTTGAATG | 55120 |
rs114768746 | snp | G/T | 0.0387552 | 0.1337 | intron-variant | FANCL | GRCh38.p7 | 2:58181949 | AAATCTTCAAATCTA[G/T]ATATTTAAATAATAT | 55120 |
rs114792936 | snp | C/T | 0.102726 | 0.202016 | intron-variant | FANCL | GRCh38.p7 | 2:58180031 | AATGAGATACTACCA[C/T]ATGCCAGTTAGAATG | 55120 |
rs114875916 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FANCL | GRCh38.p7 | 2:58166546 | GCCATCACTGACTTT[A/G]AAAATCAGTTTTTAA | 55120 |
rs114954821 | snp | A/C | 0.0429648 | 0.14013 | intron-variant | FANCL | GRCh38.p7 | 2:58191813 | CAAACTGCATTAACT[A/C]CCTACATCACTTTGT | 55120 |
rs114975892 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | FANCL | GRCh38.p7 | 2:58192202 | TTTGCCATTCCACAA[G/T]TATCTCATGTGCTCA | 55120 |
rs114979985 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58184052 | CTAAATATAACTGTT[C/T]GAAAATCCATGAAGT | 55120 |
rs115003856 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | FANCL | GRCh38.p7 | 2:58213979 | CTCTAGGGAGCATCA[C/T]TCACACAGAATGCCT | 55120 |
rs115084101 | snp | A/C | 0.192401 | 0.243274 | intron-variant | FANCL | GRCh38.p7 | 2:58179920 | GGCAAAGGATATGAA[A/C]AGACATTTCTCAAAA | 55120 |
rs115166170 | snp | G/T | 0.0236746 | 0.106192 | intron-variant | FANCL | GRCh38.p7 | 2:58182480 | AACTTTGACTTTCGT[G/T]GTTAATGTTTAAAAT | 55120 |
rs115256245 | snp | A/G | 0.0644693 | 0.167566 | intron-variant | FANCL | GRCh38.p7 | 2:58218719 | CTCTGCACGTATACT[A/G]CAACTGAACAATTAA | 55120 |
rs115262564 | snp | C/G | 0.030278 | 0.119257 | intron-variant | FANCL | GRCh38.p7 | 2:58169789 | CGAATCAATCAAGCG[C/G]AAGAAAGGATATCAG | 55120 |
rs115324140 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | FANCL | GRCh38.p7 | 2:58198201 | ATGCTTAAGGAAAAC[G/T]GAAAAAACAAAGATT | 55120 |
rs115334425 | snp | A/G | 0.079617 | 0.182947 | intron-variant | FANCL | GRCh38.p7 | 2:58218133 | TAACTGATAGTAATA[A/G]AAATATAACATCAAA | 55120 |
rs115337726 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58193797 | TGTTTGTTTTAAACT[C/T]GATTTATTTTTCTTT | 55120 |
rs115348867 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58230506 | ATTGTATAAGAAGTG[A/G]TAAGTTAATGTTCAT | 55120 |
rs115356055 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58209300 | CATTTACTGATTCAT[C/G]TGTAAGTTTCAAACA | 55120 |
rs115418056 | snp | A/C | 0.0267878 | 0.112589 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158780 | TGTTTTATATTAATA[A/C]CACTTAATTTGCTTT | 55120 |
rs115450328 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58226999 | AATCTAATTTGCTGA[G/T]ATATATTAAACTGTG | 55120 |
rs115454119 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FANCL | GRCh38.p7 | 2:58220934 | AGTGATAAGAATTGC[C/T]GGGCGTGGTGGCTCA | 55120 |
rs115481403 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | FANCL | GRCh38.p7 | 2:58222300 | TATTCTCCTGGACTA[C/T]TATGCCTATCGGAGA | 55120 |
rs115520358 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58180026 | ACCACAATGAGATAC[C/T]ACCACATGCCAGTTA | 55120 |
rs115524260 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58183772 | TTCCTGATGCTCACA[C/G]TATAGCAAAAAAATA | 55120 |
rs115536926 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58183583 | TCATTGATTTTATTC[A/T]AATCTTTCACTGGTC | 55120 |
rs115545436 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58212640 | TAAACACAAAGGACT[A/G]TTTAATTCTTATTTT | 55120 |
rs115582641 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58219926 | ATCCAAACATAAAAT[A/C]CCTACTGCATATCTT | 55120 |
rs115593449 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | FANCL | GRCh38.p7 | 2:58169696 | AAAATAACCAGGTTA[C/T]AGAAGAACATAAATG | 55120 |
rs115614677 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | FANCL | GRCh38.p7 | 2:58203995 | AAATTCTTTGAGGCT[C/T]TCCAAAATCAATGTT | 55120 |
rs115615079 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | FANCL | GRCh38.p7 | 2:58206913 | CTGTGATTATTAATA[G/T]GTTGAGTATATGCGA | 55120 |
rs115628734 | snp | A/G | 0.0260105 | 0.111035 | intron-variant | FANCL | GRCh38.p7 | 2:58167916 | AATAGTTTTTTCTCC[A/G]ACTGCTTATTTTGTC | 55120 |
rs115631570 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161184 | AACCACCTCCACCTC[A/G]GGTAAACCTATGAAG | 55120 |
rs115672138 | snp | C/T | 0.021333 | 0.101051 | intron-variant | FANCL | GRCh38.p7 | 2:58189101 | GGCCCTGGTGGAAGG[C/T]TGAGAAGGACTAAAG | 55120 |
rs115732778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58181530 | TTACAAAGAACTGAA[C/T]TCTAGTTAAATGTAT | 55120 |
rs115785010 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162561 | CAGAACCTGTGTTTA[G/T]GTGAAATCTCTGTAT | 55120 |
rs115785349 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58204739 | TAAGGAAAATGCTGT[A/C]TAAGCACAGGTACAG | 55120 |
rs115886160 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | FANCL | GRCh38.p7 | 2:58170532 | AATTTACACATAAAT[A/G]TAAACGAGCTAAATC | 55120 |
rs115903145 | snp | C/G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58237118 | GCACTCTGAACCAAT[C/G/T]TGACCTAACTGGCAT | 55120 |
rs115916037 | snp | A/G/T | 0.013097 | 0.0799021 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162437 | GAAGACCATGAAAAA[A/G/T]GTATATAGTTGACCC | 55120 |
rs115968355 | snp | A/C/T | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58183778 | ATGCTCACAGTATAG[A/C/T]AAAAAAATACATTAA | 55120 |
rs116020724 | snp | A/T | 0.0345262 | 0.126772 | intron-variant | FANCL | GRCh38.p7 | 2:58179793 | TAGAGTGAACAGGCA[A/T]TCTACATAATGGGAG | 55120 |
rs116052376 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58231722 | TACACATTAATAATA[A/T]CAGTCAAAAGTTGGA | 55120 |
rs116077643 | snp | C/T | 0.0402882 | 0.136092 | intron-variant | FANCL | GRCh38.p7 | 2:58219613 | GATGAGTCACAGAGA[C/T]AACATGTACCCTTGA | 55120 |
rs116207521 | snp | A/G | 0.0345262 | 0.126772 | intron-variant | FANCL | GRCh38.p7 | 2:58199497 | GAAGATAAAAAGAAT[A/G]AAATATCTTCTGGCT | 55120 |
rs116236096 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58205247 | TTTCAAGAAATGCAC[A/C]ATGAAGTTGTGAAAC | 55120 |
rs116263038 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58170531 | AAATTTACACATAAA[A/T]GTAAACGAGCTAAAT | 55120 |
rs116263089 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | FANCL | GRCh38.p7 | 2:58239611 | CTCTATCTTAGATAA[C/T]AGTATATCATTAAAT | 55120 |
rs116264506 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161170 | TTACTGCCACTTTCA[A/G]CCACCTCCACCTCGG | 55120 |
rs116271933 | snp | C/T | 0.0256215 | 0.110247 | intron-variant | FANCL | GRCh38.p7 | 2:58231435 | TCTAGCTTAGAGATC[C/T]GAGCCGGGAATTTGA | 55120 |
rs116360815 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58197418 | AAATGTCACTAGAAA[C/T]GTTTTTTCTCTTTGC | 55120 |
rs116387482 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | FANCL | GRCh38.p7 | 2:58218330 | TAAAAAAATATACAA[C/T]AGAGAAAATTAACAA | 55120 |
rs116389445 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58213640 | GCATTTTGGGAGGCT[A/G]AGGCAGGAGAATCAT | 55120 |
rs116418157 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58181475 | ATTTACTGGAACTTA[C/T]GGAACACTTAAGATT | 55120 |
rs116500784 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58231160 | CTCTTTAGTGACCAG[A/T]CCTTTAAATGTTGGT | 55120 |
rs116527488 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183949 | AGCCTCTCTAAGCTT[C/T]AACATTGCACCTATA | 55120 |
rs116631235 | snp | C/T | 0.0799831 | 0.183287 | intron-variant | FANCL | GRCh38.p7 | 2:58220023 | AGCAAAATAAAGTAG[C/T]TCGGTTCTAATATCC | 55120 |
rs116694085 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FANCL | GRCh38.p7 | 2:58191225 | TTAATAAATTATACT[C/T]GCATTAAAATAAATT | 55120 |
rs116787045 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58166367 | TGGAGACCTAATTAG[A/G]CAGAGTATGAAAAGG | 55120 |
rs116813954 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58234349 | TGAAATGAAAATAAA[G/T]AAAAACACAAAATTA | 55120 |
rs117006588 | snp | A/G | 0.04875 | 0.148319 | intron-variant, synonymous-codon | FANCL | GRCh38.p7 | 2:58188732 | GGTGTGAGACACTGC[A/G]ACCAGCCATAATTTT | 55120 |
rs117153514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210248 | GGACTCACAGTTCCA[C/T]GTGGCTGGGGAAGGC | 55120 |
rs117502352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226136 | AAGAGGAAATAAGAT[C/T]GGCAAAATGTTAAAA | 55120 |
rs117808081 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58179205 | TCAATCTACCACTGG[C/T]TTTCTTAACAGAATT | 55120 |
rs118086552 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58182643 | ATTTGTAACCATATT[C/G]AACAAAGTATATGAG | 55120 |
rs137870886 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58222644 | ATCTATGAAGGCTTT[A/G]AAATGTTTATGTTCT | 55120 |
rs137892912 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58193313 | ATGACACCTCAATAC[C/T]ACTGCCTAAATAAAA | 55120 |
rs137968543 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162172 | TAACTAAAGGAAAAA[G/T]AAACTCACTACCATT | 55120 |
rs137969072 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58239900 | TAAATTTAAAATATA[C/T]ACAAAATATTTTTAG | 55120 |
rs138006413 | snp | A/C/G | 0.000231248 | 0.0107506 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159493 | AGTCCAGATATATTC[A/C/G]AGAAGTCAAGATCTC | 55120 |
rs138058695 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58204919 | TACAATGGAAACCAA[C/T]ATCCTTTGAAATATA | 55120 |
rs138092430 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58216780 | CTTGACCTCTGACCT[C/T]ACCTACAACTGGGAT | 55120 |
rs138107348 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58180229 | ATTATGGGGTATATA[C/T]CCAAAGAATTATAAA | 55120 |
rs138161127 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58228480 | ACTAAAGTCCAGAGG[A/C]CAAATCCAGCTCAAT | 55120 |
rs138174507 | snp | A/C | 0.00874735 | 0.0655527 | intron-variant | FANCL | GRCh38.p7 | 2:58213426 | TTGATAGGTTTTGTC[A/C]CTCTACCAGACAGTA | 55120 |
rs138195826 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | FANCL | GRCh38.p7 | 2:58205925 | GCCACTAACTTTTCA[C/G]TTAAAAATATTTATG | 55120 |
rs138240841 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | FANCL | GRCh38.p7 | 2:58212458 | TATCATAAAGTGATA[C/T]GTATTTCTTCCAAAC | 55120 |
rs138302416 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | FANCL | GRCh38.p7 | 2:58167206 | ACAGAGCTAGACTCC[A/G]TCTCAAAAAGAAAAA | 55120 |
rs138360456 | snp | C/T | 3.31664e-05 | 0.00407211 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161524 | TTTTATTTTTTACCT[C/T]ATATAAGCATATTTG | 55120 |
rs138392448 | in-del | -/A | 0.295854 | 0.245759 | intron-variant | FANCL | GRCh38.p7 | 2:58203027 | AGGCAAATTTCTCTT[-/A]AAAAAAAAAAAAAAG | 55120 |
rs138436131 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58183451 | CCCCTTATTAGTTAC[C/T]GCTTTTATTACCAAA | 55120 |
rs138465673 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200360 | TCTGGCTGTTTCACA[C/T]GTAAAAATGACAAAA | 55120 |
rs138500831 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209275 | TAGAGGATGTTGTCA[A/G]ACTGGTTCACATTTA | 55120 |
rs138517781 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58234777 | ATATAATTGGAAACA[C/G]ACTTCTTAAAGCAAA | 55120 |
rs138568717 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58230047 | TTCAAACTGTTGGTA[C/T]TAATTTTATTTCAAA | 55120 |
rs138652533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58217901 | AAGAGATTACATACT[C/T]TTCTTAAGTGGAAAT | 55120 |
rs138696039 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198417 | AGATAACTTAAAGTA[C/T]ACAGAAGAGTGTGCA | 55120 |
rs138758285 | in-del | -/AA | 0.0520825 | 0.152737 | intron-variant | FANCL | GRCh38.p7 | 2:58191781 | AGCTCTCACTATATT[-/AA]GAGTTCACCAGTTTA | 55120 |
rs138774617 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58209791 | AAAGCTCTGGTATAA[C/T]TATTGGAATGAATTT | 55120 |
rs138781333 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58188880 | AACCCATATGCCCAT[A/C]AAAAGGTGAATGGCC | 55120 |
rs138803206 | snp | A/G | 0.0244538 | 0.107838 | intron-variant | FANCL | GRCh38.p7 | 2:58168391 | AAGCCATGAGGGACT[A/G]TGCCATGAGGAGTGG | 55120 |
rs138810712 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | FANCL | GRCh38.p7 | 2:58179707 | AAAACACCAAAAGCA[A/G]TGGCAACAAAAACTG | 55120 |
rs138882280 | in-del | -/TCTG | 0.0314385 | 0.121371 | intron-variant | FANCL | GRCh38.p7 | 2:58167418 | TCTGTTTCTCCTTTC[-/TCTG]TCTGTTTCTACATGT | 55120 |
rs138929669 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205662 | ATAGTATTAATTGAA[A/G]CAAACTTCAACAACT | 55120 |
rs139073468 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | FANCL | GRCh38.p7 | 2:58172697 | GGGGAAAAAACAGAC[C/T]AGAAAAACTGGAAAC | 55120 |
rs139096241 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214204 | GGCAATTATATTGTG[A/C]TAAGTGACATATGAT | 55120 |
rs139098267 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58185821 | CTGTTAGTTCCATGA[C/G]TAGGGAATATAATTT | 55120 |
rs139159257 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58218855 | GAGTTGTAGACATCA[C/G]TATAAAATCATGTTT | 55120 |
rs139182344 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58170379 | CTTACAAGAGCTCCT[G/T]AAGGACGCGTGAAAT | 55120 |
rs139242343 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158743 | AGTAGCTCCCGAAAC[C/T]TGCATAAGTAACCAG | 55120 |
rs139251225 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58238380 | ATCCACAGAAACAGT[A/G]AGACAATAATTGTTT | 55120 |
rs139303379 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FANCL | GRCh38.p7 | 2:58202598 | GCAAGAATATCTATA[A/G]AAGTGCTTCGTAACT | 55120 |
rs139316425 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58237671 | TCTATCTAGATGTAT[C/T]GGGGGAAAAAATGAG | 55120 |
rs139357658 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58230814 | TATCCCTTTATTGTG[A/G]TATCCTTAATTTATG | 55120 |
rs139481975 | snp | G/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58211271 | CAACATGTGGAAGCT[G/T]CCAAGGCTTGGGGTT | 55120 |
rs139586757 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | FANCL | GRCh38.p7 | 2:58202220 | GCTGGTGGTTTTATA[C/T]ATACCTATACCTTTT | 55120 |
rs139602958 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58207306 | TGTGATGATGAAGGT[A/C]TGACATATCTGCACT | 55120 |
rs139625073 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58196644 | AGACTTTCCAGTCTA[A/G]TAGAGAGTCACAAAC | 55120 |
rs139643427 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58172253 | AAGAGAGCAGTGGTT[C/T]TCTCAGCACGCACCT | 55120 |
rs139680428 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58195608 | CTGTATGACAAAATA[C/T]ATACAAAGTTAAAAG | 55120 |
rs139741069 | snp | A/G | 0.00835141 | 0.0640778 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242191 | AGCAAAGATTATTTC[A/G]TCCCCTACCCATCTT | 55120 |
rs139801716 | snp | A/C | 0.00695384 | 0.058554 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58163454 | TCAGCTCCAAGAAAG[A/C]AGCACTCAGGAAGCA | 55120 |
rs139850163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180470 | GAACAGAAAACCAAA[C/T]ACTGCATGTTCTCAC | 55120 |
rs139861630 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FANCL | GRCh38.p7 | 2:58190224 | CTTAAGTTATTTTGA[C/T]TATAACTGATCACTG | 55120 |
rs139870537 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58223624 | AGAGGCAAAGGTACA[C/T]AGCGGAAAGGCTTCA | 55120 |
rs139914601 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243038 | GCAACTCGGTAATTA[A/G]GGACGGCCATGCTAC | 55120 |
rs140052173 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58239432 | TACCTAACAGCCAAT[A/C]TGTACTCTTTAAAAA | 55120 |
rs140061002 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164430 | ATAATCTCATTTGGT[A/G]ACACATTATTTACTA | 55120 |
rs140080774 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58206768 | GTTAAACTTTAAGAC[A/G]CAATTTAAATAAAGC | 55120 |
rs140082762 | snp | A/T | 0.00119737 | 0.0244387 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159224 | AAATTACTTCTCAGG[A/T]AAAATAACACGCAAA | 55120 |
rs140088149 | snp | A/T | 0.00104247 | 0.0228067 | missense, utr-variant-3-prime, downstream-variant-500B, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58161579 | ATTATCACACACTTG[A/T]TCAGGAATGGTACCG | 55120 |
rs140127854 | snp | A/T | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58219723 | TCTAAAAAGTGTGCC[A/T]AAAATTTGACTCTAA | 55120 |
rs140159447 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58195328 | TTATAGGTAAATGAT[A/G]TATTTTTTAAACTTT | 55120 |
rs140197922 | snp | A/C | 0.0236746 | 0.106192 | intron-variant | FANCL | GRCh38.p7 | 2:58190574 | ATACCCAAAAGGGTG[A/C]TACCATCCATAAAGA | 55120 |
rs140285557 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | FANCL | GRCh38.p7 | 2:58232368 | CTTTGTTTTTAAAGA[C/G]AAAGTCACTCACAAA | 55120 |
rs140355274 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58202387 | CTAACTTTTTTTTCC[-/T]AAAAAAAAAAATTAT | 55120 |
rs140360665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197585 | ATCATACCACCTTAT[A/G]TCTATGTTATAGTTT | 55120 |
rs140428291 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58192679 | GTAGGTGGAGAAAAC[A/T]ACAAACTCCTCATTA | 55120 |
rs140547539 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58167026 | AGACCATCCTGGCCA[A/G]TAAGGTGAAACCTTG | 55120 |
rs140566807 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58208897 | ATAGAGAATCATTAG[C/T]CTCGTAGTCAAGACC | 55120 |
rs140583765 | snp | A/G | 0.030665 | 0.119967 | intron-variant | FANCL | GRCh38.p7 | 2:58176595 | TAGGAAGCTGAAACC[A/G]GATCCCTTCCTTACA | 55120 |
rs140604961 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58220257 | GGCGGTAAGGAAAAC[A/C/G]GTAAGGTAAAGAAGT | 55120 |
rs140705196 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58227259 | TACAAGGTGCTTTTT[C/T]AGTTTAGCCATCCAT | 55120 |
rs140717930 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58174316 | ACAGAACTTTCCACC[A/C]CAAATCAACAGAATA | 55120 |
rs140758986 | snp | C/G | 1.65641e-05 | 0.00287781 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160176 | TTAGTAGTCCTCTCA[C/G]CCACTGCAAATTTTA | 55120 |
rs140863033 | in-del | -/TA | 0.00279162 | 0.0372561 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163250 | GTCATTTAAAATAAC[-/TA]TCATTATTGCGGTGA | 55120 |
rs140906758 | in-del | -/TATATATAT | | | intron-variant | FANCL | GRCh38.p7 | 2:58219173 | AAAAAAAAAAAAAAA[-/TATATATAT]ATATATATATATATA | 55120 |
rs140991591 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58187788 | TATACATAAAACAAC[A/G]TCCATTTTGAGTTTT | 55120 |
rs140999751 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192196 | GAGAGCTTTGCCATT[C/T]CACAAGTATCTCATG | 55120 |
rs141022778 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205126 | TGATAGTAAGACCCA[C/T]TGGAGTTCAGAATAT | 55120 |
rs141026552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231422 | CTGTGACCTCTTCTC[C/T]AGCTTAGAGATCTGA | 55120 |
rs141039576 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | FANCL | GRCh38.p7 | 2:58239156 | CAAAAGTCAATGGAC[A/G]CTAAAACCAGAGAAT | 55120 |
rs141101121 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58181400 | TTTACTAGGATGGGA[A/C]AAAACCCTGTGATGT | 55120 |
rs141136735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58233707 | AGGAAAAAAAATGCA[C/T]GGGAGAGAGACTGGG | 55120 |
rs141162289 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58204315 | TGAAATGAAAATATT[C/T]GCTATATTCCTATTA | 55120 |
rs141248677 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58199712 | ATGATTTCTCTATAA[C/T]CCAATTCTGATTCTT | 55120 |
rs141272602 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58180048 | TGCCAGTTAGAATGG[C/T]GATCATTAAAAAGTC | 55120 |
rs141292416 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58210017 | AAAAGTTCAACTAGT[C/T]GAAGTGTACTCACTC | 55120 |
rs141347170 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | FANCL | GRCh38.p7 | 2:58172861 | AGGAGGAAATTCAAA[C/T]CAAAGGCGAAGAAGC | 55120 |
rs141362977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221838 | ACTCTAGTTACAATT[A/G]AACACTTTGACTAAA | 55120 |
rs141366677 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | FANCL | GRCh38.p7 | 2:58171620 | TAACAAAATAGGGGA[C/T]TGGAGCCAAGATGGC | 55120 |
rs141366710 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214973 | ACTTCTCTCAACCAT[C/G]TCAGATCCACTGAGG | 55120 |
rs141390750 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FANCL | GRCh38.p7 | 2:58201169 | CTTGATCAAAATTAA[A/G]ATACTTTTCAATAAT | 55120 |
rs141400460 | snp | C/T | 0.000164829 | 0.00907674 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204214 | ACTGAAGCAGGTATC[C/T]GCATACACAAGTCTG | 55120 |
rs141429372 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58212375 | CCCTCCTGCAACACA[A/T]GGGAATTGTGGGAGT | 55120 |
rs141444545 | snp | C/G/T | 1.65611e-05 | 0.00287755 | missense, utr-variant-3-prime, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58162925 | CATCTTTCAAATTTT[C/G/T]TAACACACTATTTTC | 55120 |
rs141446906 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58212107 | AAGACATACCCAAGA[C/T]TGGGCAATTTACAAA | 55120 |
rs141488669 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58188969 | CAACATGGTTGAATC[A/T]CCAAGTAATTCTGCC | 55120 |
rs141581300 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58185242 | GCAAGCATAAAGATA[G/T]TAAGAGATCAATCCA | 55120 |
rs141582536 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58182534 | TAAATTTTGGAATTT[C/T]TGAGGGGTATACAAT | 55120 |
rs141671889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58228011 | AATCAGGCAACTCTA[C/T]GTAATTTTTAAAATC | 55120 |
rs141692533 | snp | A/C | 0.0376037 | 0.131863 | intron-variant | FANCL | GRCh38.p7 | 2:58190052 | ATCAGGTATCTTTAA[A/C]CAGGTGATAAATCTA | 55120 |
rs141709023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206935 | TATATGCGACCTTGA[C/T]TGTCAATTGCCCTCT | 55120 |
rs141799018 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58184507 | AAGATCCAAAAATTA[C/T]AACCAGAACTTTGCA | 55120 |
rs141854952 | snp | C/T | 0.0322114 | 0.122752 | intron-variant | FANCL | GRCh38.p7 | 2:58174960 | agggtacatcaccac[C/T]gatcccacagaaata | 55120 |
rs141921354 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58236452 | ATATTATAAACCCTT[C/T]AAGCAACTAGTTAAA | 55120 |
rs141947791 | snp | C/T | 0.0314385 | 0.121371 | intron-variant | FANCL | GRCh38.p7 | 2:58171805 | AAGCAGGACGAGGCA[C/T]TGCCTCCCTCGGGAA | 55120 |
rs141957751 | snp | C/G | 0.0287284 | 0.116357 | intron-variant | FANCL | GRCh38.p7 | 2:58170877 | AGATTCATAAAGCAA[C/G]TTCTCAGAGACCTAC | 55120 |
rs141981852 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58169138 | GCAGGGGTCAAAAGA[C/G]AACTCATACAGGAGA | 55120 |
rs141995884 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FANCL | GRCh38.p7 | 2:58166557 | CTTTAAAAATCAGTT[C/T]TTAAACAAAGGAGTT | 55120 |
rs142083861 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213819 | CAGATTTTGAAACTC[C/T]CCAAGGGTGTGTTAA | 55120 |
rs142110072 | snp | C/G | 6.58946e-05 | 0.0057396 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165766 | TCCGTGGAGGTTTTT[C/G]TGGCTCAAGTACCCA | 55120 |
rs142129291 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58221193 | ACTCGGTCTCAAAAA[A/G]AAAAAAGTGATAAGA | 55120 |
rs142144780 | snp | A/T | 0.0287284 | 0.116357 | intron-variant | FANCL | GRCh38.p7 | 2:58170307 | CAGGAGTGAAGGAGA[A/T]ATAAAATCCTTTACA | 55120 |
rs142307707 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | FANCL | GRCh38.p7 | 2:58228893 | CCATTTTTTCCCATG[C/T]TATTTCAATATGTCA | 55120 |
rs142326597 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191840 | TTGTACATTTGTACA[A/G]CATTTTACAATTCAA | 55120 |
rs142400219 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58223110 | ATTAACGGGAACTAC[C/T]TCAATTTCGTTCTGA | 55120 |
rs142450255 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | FANCL | GRCh38.p7 | 2:58216716 | ACAAAAAAGTGAAAA[C/G]AGAATGCACACTGTC | 55120 |
rs142489387 | in-del | -/GG | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58222567 | ACTATTCTTCAAGCA[-/GG]TAAGTCGGAGTATTA | 55120 |
rs142670244 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58197874 | GTAATCAATGTCAAA[A/G]GTTTTAGCAATATAA | 55120 |
rs142725516 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58209415 | TAATTTGCAGTTATT[C/T]AATGACATGGATTTA | 55120 |
rs142738380 | in-del | -/GA | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58219383 | AAAAAACAAATAAAT[-/GA]GAGGGAACAAAATCT | 55120 |
rs142783303 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58213310 | AGTATGTGGACAGCA[C/T]AGTTCAGGTCTCAGC | 55120 |
rs142816428 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206046 | AATGTAAATATATTT[A/G]ACTACTACAATTTAA | 55120 |
rs142945012 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180701 | TACCAGAACTTAAAA[C/T]ATAATTAAAAAATAA | 55120 |
rs142964585 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58224264 | CTCTCCTTGTATTTG[C/T]ATTGTTTATTAAAAT | 55120 |
rs143082539 | snp | A/C/T | 0.00279258 | 0.0372817 | intron-variant | FANCL | GRCh38.p7 | 2:58167850 | TCTTAGCAATTTCAA[A/C/T]GAACTTAGGGGGTAG | 55120 |
rs143135118 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58221813 | TTCACAGCAACAATA[A/G]GGATCAAATACTCTA | 55120 |
rs143166971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58194469 | AGATGTTCTCATCGT[C/T]TATGCTAAAATCTAT | 55120 |
rs143177644 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161074 | TCAACATGAAAAGTA[C/G]TAGTATTGGATATAT | 55120 |
rs143256614 | in-del | -/ATA | 0.290718 | 0.246662 | intron-variant | FANCL | GRCh38.p7 | 2:58200866 | TAATACAATATGTAT[-/ATA]ATAATAAATTAGACT | 55120 |
rs143259350 | snp | C/G | 0.0232847 | 0.105357 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241434 | CGGGAAGATCCTGGA[C/G]GATTCCGCGGGCGGA | 55120 |
rs143259414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58190235 | TTGACTATAACTGAT[C/T]ACTGATCACCCATCA | 55120 |
rs143298130 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58237802 | CCTCCTTTTGAATAT[A/T]GACTAAGAAACTTGC | 55120 |
rs143324438 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208522 | AAATGTGTTTTACAT[A/G]GCTCATAAAATACTG | 55120 |
rs143346791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58197068 | TTTACTTATAGCATA[C/T]ATCAAAATACCAAAA | 55120 |
rs143387573 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243140 | GTCCCTTACTTCAAG[C/T]ACTTTATAATTTATC | 55120 |
rs143481866 | snp | G/T | 0 | 0 | intron-variant | FANCL | GRCh38.p7 | 2:58239245 | GGAGACTCTGACAGA[G/T]GATACCTTAACCAGG | 55120 |
rs143493708 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FANCL | GRCh38.p7 | 2:58236331 | CAGTGAAGTAACATC[C/T]TTACAGTATCAAAAG | 55120 |
rs143549675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162258 | TATAGTGGTATCTAT[C/T]CAATTTTGAGAAACT | 55120 |
rs143554474 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58184090 | GCTTTCCCCTTAAAA[C/G]TACCAAGATTCCCTT | 55120 |
rs143600383 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58228358 | ATTCACATCTTAACA[C/T]AGCTTTGAGTGGGTC | 55120 |
rs143632750 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58198961 | GTGAACCTGGGAGGC[A/G]GAGATGGCAGTGAGC | 55120 |
rs143640170 | snp | C/T | 0.021333 | 0.101051 | intron-variant | FANCL | GRCh38.p7 | 2:58174654 | GTGTGTAGAGGGAAA[C/T]TTATAGCACTAAATG | 55120 |
rs143660630 | snp | A/C/G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58216137 | ATCTACCAGGGGGGA[A/C/G/T]ATCCCAATGAATATA | 55120 |
rs143677901 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | FANCL | GRCh38.p7 | 2:58172256 | AGAGCAGTGGTTCTC[C/T]CAGCACGCACCTGGA | 55120 |
rs143678263 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58216880 | GAGGAGAAGAGGCTC[A/G]CTTCTCTACCATCCT | 55120 |
rs143710592 | snp | G/T | 0.0185938 | 0.0946107 | intron-variant | FANCL | GRCh38.p7 | 2:58164561 | CTTGTTCAAAACTTG[G/T]TCTTAAGAAAGCAAA | 55120 |
rs143716073 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58213437 | TGTCACTCTACCAGA[C/G]AGTAATGGATTAACA | 55120 |
rs143739412 | in-del | -/T | 0.153665 | 0.230694 | intron-variant | FANCL | GRCh38.p7 | 2:58205165 | GGAAATATATTTTTT[-/T]AATATCACTATATGC | 55120 |
rs143819820 | snp | C/G | 0.000913371 | 0.0213507 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58229827 | ACCTGTTGTACTATT[C/G]GATGGTATCCACTAA | 55120 |
rs143841381 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58219780 | ACATAGTCAATTACA[C/T]AGTTCACATTATTCA | 55120 |
rs143878610 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58215087 | TTCCAACTATGCTCT[A/T]AAAAACAAATATTAA | 55120 |
rs144020929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200408 | CAAAATCTCTTTTCC[C/T]TCTAAAATGTCAAAA | 55120 |
rs144032812 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58219454 | AAAGGAGGTGTGAGC[A/G]TAACTGCCCACTCCT | 55120 |
rs144057264 | snp | A/C/T | 0.000341148 | 0.0130561 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241310 | TCGCTTCCGTCACCG[A/C/T]CATGGCTCGAAGTCC | 55120 |
rs144081841 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58238637 | CTAAAACTGATTACA[C/T]ATTAGGTCACAGGAA | 55120 |
rs144113658 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | FANCL | GRCh38.p7 | 2:58195386 | AAAACTGTGAAATCA[G/T]CCCCCAACCCGCACA | 55120 |
rs144155158 | snp | A/C/G | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58172524 | TAGCAAACTCCAACA[A/C/G]ACCTGCAGCTGAGGG | 55120 |
rs144175012 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58213535 | TTTATTTTTAAACAG[C/T]ATAAAACAAATGATT | 55120 |
rs144246902 | snp | C/G | 0.0240643 | 0.107019 | intron-variant | FANCL | GRCh38.p7 | 2:58170913 | GACTTAAGACTCCCA[C/G]ACAATAATAGTGGGA | 55120 |
rs144264463 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | FANCL | GRCh38.p7 | 2:58238517 | GTAAATAACTTTAAG[C/T]CAATAAAATCAGAAA | 55120 |
rs144280273 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | FANCL | GRCh38.p7 | 2:58202231 | TATATATACCTATAC[C/T]TTTTTCCTAAAAAAA | 55120 |
rs144304783 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58172009 | TTGCTAGCACAGCAG[C/T]CTAAGATCAAACTGC | 55120 |
rs144350768 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58186284 | AATTTTCTTTAAGAA[A/G]GTAAATTTCTGGGCC | 55120 |
rs144369127 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214648 | CCGAGAAGCTAGGTG[C/T]GTACCACCACACCTA | 55120 |
rs144452260 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58218567 | ACATTGAAGTGGGTG[C/G]AGGAAATGGTTCTAA | 55120 |
rs144593535 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58231429 | CTCTTCTCTAGCTTA[A/G]AGATCTGAGCCGGGA | 55120 |
rs144606047 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58229587 | TAAGGGTGAATGCAT[C/T]TGAAGAACCTAAAGT | 55120 |
rs144630318 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58227520 | CCAACCACCCTGGTC[A/G]AACTCCACGTCATTC | 55120 |
rs144711392 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58196463 | ATAACACTCATTACT[A/G]CGAATTCTACATTTT | 55120 |
rs144729980 | snp | C/G | 1.65795e-05 | 0.00287914 | splice-donor-variant, intron-variant | FANCL | GRCh38.p7 | 2:58226727 | AAAAAAAAATTCTTA[C/G]CAAAAGCATCTTCAA | 55120 |
rs144750713 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58210003 | CCAAGACAAACTTGA[A/G]AAGTTCAACTAGTTG | 55120 |
rs144788015 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192305 | AGCGATATAATATCT[A/T]CTTTAATCTGGCAAG | 55120 |
rs144794665 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58223795 | TATACTGAACTCCCA[C/T]TATATGCAGTAATTA | 55120 |
rs144838391 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163276 | CGGTGAACCGAGATC[A/G]CGCCATTACACTACA | 55120 |
rs144859826 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205811 | ACTGATATACTGGCA[A/G]AAATTATGGGAATTT | 55120 |
rs144880878 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, stop-gained | FANCL | GRCh38.p7 | 2:58188692 | CAATCTTCTCGTCTC[A/G]GCCTCCTGAAGTGTT | 55120 |
rs144914389 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | FANCL | GRCh38.p7 | 2:58186867 | CAAAACCAGAATGAG[A/G]TATCATCTCACACCA | 55120 |
rs144960637 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | FANCL | GRCh38.p7 | 2:58172785 | GAACAAAGCTGGACA[A/G]AGAATGACTTTGACG | 55120 |
rs144976716 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166527 | TCACTAAATAATAAG[C/T]AATGCCATCACTGAC | 55120 |
rs144987710 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58209516 | TGCTATTATGTTTTA[C/T]AAAAAATTATCATTA | 55120 |
rs145008497 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188290 | AAAATACCATATTAT[A/C]CTGAAAAAAGTAGAT | 55120 |
rs145047020 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58202914 | TCTTCATAGAAAAAC[A/G]GCTAATTTTACTAAG | 55120 |
rs145069504 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58208191 | CATCATTGGAAAGCT[C/G]AAATTTTTAAATAAA | 55120 |
rs145149543 | snp | C/G | 0.0399052 | 0.1355 | intron-variant | FANCL | GRCh38.p7 | 2:58171669 | GTCTACAGCTCCCAG[C/G]GTGAGCGACGCAGAA | 55120 |
rs145181728 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | FANCL | GRCh38.p7 | 2:58220903 | AATACTAAAATACTA[C/T]TGATAACGGTTAAGA | 55120 |
rs145207067 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58192809 | CAAAAGTGTTTGCCC[A/C]TGGAGAAACAGGTGA | 55120 |
rs145247181 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58189081 | GCACATCAGTAGTTG[A/C]CTGAGGCCCTGGTGG | 55120 |
rs145260146 | snp | C/T | 4.96405e-05 | 0.00498175 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160148 | AATATGATGTTAAAA[C/T]TCTGTCTACTAGTTA | 55120 |
rs145284589 | snp | A/G | 0.000724996 | 0.0190256 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58204199 | TTTTAACTTGATGGT[A/G]CTGAAGCAGGTATCC | 55120 |
rs145289000 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58170548 | TAAACGAGCTAAATC[C/T]CCCAATTAAAAGACA | 55120 |
rs145323530 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58190793 | ACTGTCTCAGTGTCT[C/T]TACTATTTACAAACT | 55120 |
rs145384368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187279 | TGGGACACGGATGAA[A/G]CTGGAAACTATCATT | 55120 |
rs145433774 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58179243 | AACTACTTTACATTT[C/T]ATATGGAACCAATAA | 55120 |
rs145444832 | in-del | -/A | | | intron-variant | FANCL | GRCh38.p7 | 2:58170695 | CAAAAAAAAAAAAAA[-/A]GCATGGTTTGCAATA | 55120 |
rs145482520 | snp | A/C | 0.138207 | 0.223612 | intron-variant | FANCL | GRCh38.p7 | 2:58179608 | ATTAAAGACTTAAAC[A/C]TAAGACCTAAAACCA | 55120 |
rs145538828 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58211638 | GCTGTTTCCCTTTTA[A/G]AACTAAATGCTTTTA | 55120 |
rs145556232 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58228348 | AACACATATGATTCA[C/T]ATCTTAACATAGCTT | 55120 |
rs145593858 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243279 | TTTTTGGAAAGCTTT[C/T]TTAATCTTCTGAAAA | 55120 |
rs145613714 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58165964 | CTCAATTTAGAAATT[C/T]TAAGCTGTTTCATTT | 55120 |
rs145652829 | in-del | -/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58227886 | ATCATTACTTTTTTT[-/T]AAAGAAGAAGAGAAA | 55120 |
rs145849604 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166711 | ACAAACGTTTTCAAT[C/T]TGAAATAACTGGCCA | 55120 |
rs145889270 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58215317 | CCAACCATCCCAAAT[C/T]CTACTCAAGACTAAT | 55120 |
rs145894926 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58209067 | AAAGCTTATCCCAAC[A/T]TTCATCTCCTCTAAG | 55120 |
rs145901525 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58240430 | AGAGAAAAAAATCCA[C/G]GACTGAAATCACACA | 55120 |
rs145940452 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58180465 | TCAGTGAACAGAAAA[C/T]CAAACACTGCATGTT | 55120 |
rs145965887 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58223175 | GAAAACAGATCCGTA[C/T]AGCTGAGAATATCAA | 55120 |
rs145977166 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58219699 | TATAAATCCTATATC[C/T]AGCATGGCTCTAAAA | 55120 |
rs146000574 | in-del | -/T | 0.138886 | 0.22395 | intron-variant | FANCL | GRCh38.p7 | 2:58199826 | TCATTTGACAAATTA[-/T]TTAAAAGAAGTTTTA | 55120 |
rs146049339 | snp | A/C | 0.0123036 | 0.0774623 | intron-variant | FANCL | GRCh38.p7 | 2:58168363 | TTGGGGAGCTCCCTC[A/C]CCTAGCCAAGGGAAG | 55120 |
rs146061251 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164327 | TGGCATCAACATAAA[C/T]GCAGTTATTGCATAT | 55120 |
rs146089611 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206479 | AGAGGGAGAGAGAAG[A/G]CATGCACGTTTAAGA | 55120 |
rs146100716 | snp | A/T | 0.0260105 | 0.111035 | intron-variant | FANCL | GRCh38.p7 | 2:58202380 | TCTAGAACTAACTTT[A/T]TTTTCCTAAAAAAAA | 55120 |
rs146149869 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58172545 | CAGCTGAGGGTCTCT[A/G]TTAACAGAGGGTCTG | 55120 |
rs146210982 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58185256 | ATTAAGAGATCAATC[C/G]AATATTAAGTTCTCC | 55120 |
rs146295528 | in-del | -/TATT | 0.030278 | 0.119257 | intron-variant | FANCL | GRCh38.p7 | 2:58220587 | ATATGTTTAAGTCTC[-/TATT]TAGTTTTTCTTTAGT | 55120 |
rs146331813 | snp | C/G | 0.0150606 | 0.0854603 | intron-variant | FANCL | GRCh38.p7 | 2:58169150 | AGACAACTCATACAG[C/G]AGAGCTCCAGCTGGC | 55120 |
rs146341935 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | FANCL | GRCh38.p7 | 2:58165356 | CCAGATCTGAGCACA[C/T]TAATCTGAGAAGATT | 55120 |
rs146346554 | snp | A/G | 0.0103295 | 0.0711199 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242588 | ATATCCTTATCTCTA[A/G]AGAAACGGAGACATA | 55120 |
rs146396399 | snp | G/T | 0.000264809 | 0.0115037 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159653 | GCATCATCATACCTG[G/T]CCTTTTGATGTTAGT | 55120 |
rs146490400 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239087 | ATAAATATAGAAATG[A/G]CAAGAGTTAGAAAAT | 55120 |
rs146491823 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160679 | ATTTTTAAAAATTAA[A/G]TGAATATTCATAATT | 55120 |
rs146502273 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58233397 | AAAATTAGCTTTTTA[C/G]TTAAAGTATCTAGAA | 55120 |
rs146525828 | in-del | -/AAAAGT | 0.356383 | 0.226236 | intron-variant | FANCL | GRCh38.p7 | 2:58205360 | AGGGTCTTAGAAAAC[-/AAAAGT]AAAACTATTCTAGAA | 55120 |
rs146574564 | snp | G/T | 0.00835141 | 0.0640778 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159201 | AAATCTTTAAGATCT[G/T]TACCTAAAAATTACT | 55120 |
rs146584635 | in-del | -/T | 0.0517044 | 0.152246 | intron-variant | FANCL | GRCh38.p7 | 2:58213197 | ATACATTTAAATCAA[-/T]TCTGTCATGCAAATC | 55120 |
rs146610750 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58214701 | GTATTTTGTAGACAC[G/T]GGGTTTCACCATGTT | 55120 |
rs146626544 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58216756 | ATTCACACACAGGTA[A/C]CTTCATACCTTGACC | 55120 |
rs146690827 | snp | A/C/G | 4.99616e-05 | 0.00499787 | missense, utr-variant-5-prime, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58241286 | GCAGGGGGCACTGGC[A/C/G]CAACAGGCTCGCTTC | 55120 |
rs146704095 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162557 | GATGCAGAACCTGTG[C/T]TTATGTGAAATCTCT | 55120 |
rs146741933 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58192398 | ACCATTGGTATTTTA[C/G]TATATGGAGGTTGAA | 55120 |
rs146799435 | in-del | -/TTAT | 0.0509478 | 0.151255 | intron-variant | FANCL | GRCh38.p7 | 2:58206326 | TTGCATGTAGGCAGA[-/TTAT]TTAGAAACATGGAAG | 55120 |
rs146941075 | snp | A/T | 0.0162398 | 0.0886349 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161872 | AAACACAAGGTAAGA[A/T]CAGGAAGAATGTTTT | 55120 |
rs146951139 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58204873 | AGCACAACTGCTTTG[G/T]CTTTAAGTTACCCTA | 55120 |
rs147056032 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58183144 | ATATTGGACAAAGGA[C/T]TGATACCCTTAATAT | 55120 |
rs147079306 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | FANCL | GRCh38.p7 | 2:58199979 | TAGCTACAATAATAA[C/G]TTGGCTAAAAAGATT | 55120 |
rs147194163 | snp | C/T | 0.0479149 | 0.147179 | intron-variant | FANCL | GRCh38.p7 | 2:58176578 | AACTGGCTAGCTATA[C/T]GTAGGAAGCTGAAAC | 55120 |
rs147217236 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58172314 | TAAGTGGGTTCTTGA[C/G]CCCTGACCCCTGAGC | 55120 |
rs147305683 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58237214 | CCAGGATAGACTATA[C/T]TATTGGTCATAAAAT | 55120 |
rs147410804 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58213369 | TTTATCAGTGTATGT[A/G]TGTACCAGACCTAAT | 55120 |
rs147428564 | snp | C/G | 0.0111196 | 0.0737302 | intron-variant | FANCL | GRCh38.p7 | 2:58210444 | CACATGAGAACTGTG[C/G]GAGTACAATTCAAGA | 55120 |
rs147510451 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58194750 | ATCTTCAGCTTGACA[C/T]TGTGCAAGTTATAAT | 55120 |
rs147533365 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58190248 | ATCACTGATCACCCA[A/T]CATTTAAAAAATCTG | 55120 |
rs147542926 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58238091 | TAGCTTGACCAACTG[A/G]CAGCCCAGGACAGCT | 55120 |
rs147566803 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58166538 | TAAGTAATGCCATCA[C/T]TGACTTTAAAAATCA | 55120 |
rs147566894 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58210920 | GATTTTGCAGGGTAT[A/G]GCACCCCCACCCGGC | 55120 |
rs147576475 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58208222 | ATGCTAGCAATAAGC[C/G]CACAAAATAAGAATT | 55120 |
rs147648944 | snp | A/G | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58170799 | TACATAATGGTAAAC[A/G]GATCAATGCAACAAG | 55120 |
rs147757782 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58226926 | AAGAAATGAAGTATC[A/G]GTCATCAACTTTACT | 55120 |
rs147775451 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58203928 | GTATTTTGAGCAAAT[C/T]TGGACTAAAATATGA | 55120 |
rs147811379 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, synonymous-codon, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159432 | ACAAAAAATCAGCTA[C/T]ACACAATTCCCAAAC | 55120 |
rs147857359 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207798 | GCATAATGACTCATG[C/T]CTATAATCCCAGCAC | 55120 |
rs147860433 | snp | C/T | 4.96208e-05 | 0.00498076 | missense, downstream-variant-500B, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58160135 | TGGACATTCACCAAA[C/T]ATGATGTTAAAACTC | 55120 |
rs147881438 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58182463 | AAGAACATTTTCATC[A/G]TAACTTTGACTTTCG | 55120 |
rs147881643 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58231587 | AGGCAGAATTGAGAT[C/T]TGGGGTGGTACCTAA | 55120 |
rs147891737 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | FANCL | GRCh38.p7 | 2:58227635 | TGTGTGTTCCTCCAC[C/T]GATATATTTCTCTCA | 55120 |
rs147963883 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | FANCL | GRCh38.p7 | 2:58187111 | CTATAAAAACACATG[C/T]ACACATATGTTTATT | 55120 |
rs147988854 | in-del | -/CTAA | 0.00993419 | 0.0697739 | intron-variant | FANCL | GRCh38.p7 | 2:58193968 | TGCTAGTATACTGCT[-/CTAA]CTAATGGATAATGCT | 55120 |
rs148000877 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58189342 | ACAGCAGTAGATGTG[C/T]AGAAACTAACAGCTT | 55120 |
rs148010641 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58236423 | TAAGGCAGACCATGA[C/T]AGATTTAATATGTAT | 55120 |
rs148047915 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58184383 | TATTATTGTCTAAAA[C/T]ATGGGAGAAAAACTG | 55120 |
rs148083066 | snp | A/G | 0.107694 | 0.205546 | intron-variant | FANCL | GRCh38.p7 | 2:58174887 | CAAAATTGATAGACC[A/G]CTAGCAAGACTAATA | 55120 |
rs148106268 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58216698 | TATGACAATAAACCA[C/T]ACACAAAAAAGTGAA | 55120 |
rs148143865 | snp | A/G/T | 0.00953873 | 0.0683987 | intron-variant | FANCL | GRCh38.p7 | 2:58171613 | AAAAGAGTAACAAAA[A/G/T]AGGGGATTGGAGCCA | 55120 |
rs148168997 | snp | C/G | 0.00438332 | 0.0466095 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241850 | CAGATATATTTGAGG[C/G]ACACACATGTATACG | 55120 |
rs148178058 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58163298 | TACACTACATACTGG[A/G]CAACAAGAGCAAAAC | 55120 |
rs148197441 | snp | A/G | 1.65127e-05 | 0.00287334 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159583 | ACTGGACTTTGGCCT[A/G]CAATTTCCCAGTTTA | 55120 |
rs148266261 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221817 | CAGCAACAATAAGGA[A/T]CAAATACTCTAGTTA | 55120 |
rs148294330 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58212213 | GCAAGTCCCATCTTA[C/T]ATGGATGGCAGCAGG | 55120 |
rs148379449 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200812 | GTCCAGTATGTAGTT[C/T]CTGAGATAATGACAT | 55120 |
rs148383677 | in-del | -/TTA | 0.377385 | 0.215112 | intron-variant | FANCL | GRCh38.p7 | 2:58165663 | CTGTCATTGTTAGAT[-/TTA]TTTTCATAATACAAA | 55120 |
rs148396470 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | FANCL | GRCh38.p7 | 2:58177917 | GGGGATATCGCCACT[C/G]ATCCTACAGAAATAC | 55120 |
rs148516173 | snp | C/G | 0.00013293 | 0.00815153 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232067 | ACCTTGCATTCTTCA[C/G]TTGTAAATCTTCAGG | 55120 |
rs148537981 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58177513 | GGAAATCATCATTCT[A/C]AGTAAACTATCGCAA | 55120 |
rs148544500 | snp | A/G | 0.0209421 | 0.100162 | intron-variant | FANCL | GRCh38.p7 | 2:58170278 | AGAATTTCCTATCCC[A/G]CCAAACTAACCTTCA | 55120 |
rs148559377 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180613 | CCTAATGTAGATGTC[A/G]GGTTGATGGGTGCAG | 55120 |
rs148568925 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58223925 | AGTATAGGAACCCTA[A/T]TACTTACAATACAGC | 55120 |
rs148611538 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58213560 | ATGATTAAGTAACAG[C/G]AGCTAAATCGAAAGT | 55120 |
rs148658317 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58210015 | TGAAAAGTTCAACTA[C/G]TTGAAGTGTACTCAC | 55120 |
rs148734531 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | FANCL | GRCh38.p7 | 2:58191687 | AGATAATAATTGCTG[C/T]CTGACAGATATGTGT | 55120 |
rs148744282 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58238625 | TAGAGACAACACCTA[A/G]AACTGATTACATATT | 55120 |
rs148788519 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186434 | GTATGGGGAAAATTT[A/C]TTGGAAGTGAACTCA | 55120 |
rs148836795 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | FANCL | GRCh38.p7 | 2:58234955 | TAAACAATAGGCAGC[A/G]AGGACAGTGATCCTT | 55120 |
rs148851845 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58170986 | ACACAAAATTAACAA[G/T]GATATTCAGGAGTTG | 55120 |
rs148873430 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58183932 | TTAAGCAAGACATAC[A/T]CAGCCTCTCTAAGCT | 55120 |
rs148883624 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58228349 | ACACATATGATTCAC[A/G]TCTTAACATAGCTTT | 55120 |
rs148905152 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166443 | TTTTCCACATTTAAC[G/T]TTTAGCCAATCTCTG | 55120 |
rs148909230 | snp | C/T | 0.0166325 | 0.0896639 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58243336 | TATTTCCTGCTGCAT[C/T]GTAGGTGCTAATAAA | 55120 |
rs148926504 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58215598 | CAGAAGTGAAGTAAG[A/C]CAACATTCTGAAGCC | 55120 |
rs148979426 | snp | C/T | 0.0592355 | 0.161582 | intron-variant | FANCL | GRCh38.p7 | 2:58211980 | AAACCGTTCCAACCT[C/T]TGCCTGCTACCCAGT | 55120 |
rs149030855 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58168898 | CAGACTGCCTCACCA[C/G]ATTCCTCCTCTCTGG | 55120 |
rs149065111 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58208473 | TGTTGTCCCTGTTAA[C/T]AGCTGAATGTCAACA | 55120 |
rs149094519 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, downstream-variant-500B | FANCL | GRCh38.p7 | 2:58188432 | TCTCTTAATTTCGGG[G/T]TTTTTTTGTTTTTTG | 55120 |
rs149102677 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160760 | TTTCTGTAATTTCAT[G/T]ATTTTATATAAGGTA | 55120 |
rs149111862 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58202933 | AATTTTACTAAGGTA[C/G]AAAATATAAACAAAT | 55120 |
rs149233318 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58218025 | AAAAGTAGACTTAAA[A/C]TGGAACTCAATAACC | 55120 |
rs149328692 | snp | C/T | 0.021333 | 0.101051 | intron-variant | FANCL | GRCh38.p7 | 2:58177727 | CATGGCACATGTATA[C/T]ATATGTAAGTAACCT | 55120 |
rs149380816 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58209863 | CTTCAAATGCATTAA[C/T]AATTATACAAAATAT | 55120 |
rs149391157 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58223755 | GGATTATTTTAAATA[C/T]AGGTAATTGTTCACT | 55120 |
rs149412402 | snp | C/G | 0.0133875 | 0.0807127 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162834 | TCATTATGCAATACT[C/G]TCTGGAATATCAAAA | 55120 |
rs149414332 | snp | C/T | 9.9108e-05 | 0.00703876 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58221973 | TTCCTATCTCTTCAA[C/T]AAGGCTTGAGTAGAA | 55120 |
rs149435269 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205670 | AATTGAAGCAAACTT[A/C/T]AACAACTTTTAGGAA | 55120 |
rs149446792 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | FANCL | GRCh38.p7 | 2:58180333 | CCCAAACGCCCATCA[A/G]TGATAGACTGGAAAA | 55120 |
rs149447347 | in-del | -/G | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58204631 | TTTAATGCTCCCTTT[-/G]TTTTTCTCCTCAATG | 55120 |
rs149451697 | snp | A/C | 0.0001156 | 0.00760176 | utr-variant-3-prime, missense, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159554 | GCACGGGGATCACAG[A/C]CTTAGAAAGTTCAAC | 55120 |
rs149465674 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58193783 | TTGCCCCAACACTGT[G/T]TTTGTTTTAAACTCG | 55120 |
rs149593945 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58171959 | AGGAGATTACATCCC[G/T]CTTGGAGAGTCCTAC | 55120 |
rs149603717 | in-del | -/A | 0.0644693 | 0.167566 | intron-variant | FANCL | GRCh38.p7 | 2:58219664 | AGAACAAAAGTCAGG[-/A]TAAGATTAGCATACA | 55120 |
rs149625498 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | FANCL | GRCh38.p7 | 2:58231178 | TTTAAATGTTGGTAC[A/G]CCCCAAGGTCTTGTC | 55120 |
rs149687522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58211408 | GACCCTGTGCCCACT[C/T]TTTCCTCCTACACCT | 55120 |
rs149726602 | snp | C/G | 0.0026813 | 0.0365165 | missense, intron-variant, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58232101 | CACTATCCTAAGGTG[C/G]AAGTCTCTTCCCTGT | 55120 |
rs149731356 | snp | C/T | 0.00884017 | 0.0658934 | missense, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58165745 | CAATTCTGCGTGCTG[C/T]TGCACTCCGTGGAGG | 55120 |
rs149741023 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207424 | ATGTCAATAGCCACA[C/T]ATGGCTACTGAACAA | 55120 |
rs149765637 | in-del | -/AG | | | intron-variant | FANCL | GRCh38.p7 | 2:58212422 | TTTGGGTGGGGACAC[-/AG]GGGATACAGAACCAA | 55120 |
rs149782988 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58196147 | AGAGACTGCAAATAT[A/G]GCATAAACAAATATG | 55120 |
rs149803148 | snp | C/G | 0.000753788 | 0.0193991 | missense, utr-variant-3-prime, nc-transcript-variant | FANCL, VRK2 | GRCh38.p7 | 2:58159778 | TTTCAGTGTTTCCTT[C/G]CAGACATTTTTAAGG | 55120 |
rs149883795 | in-del | -/AATT | 0.144969 | 0.226867 | intron-variant | FANCL | GRCh38.p7 | 2:58204342 | TTAATCCATTATAAA[-/AATT]AATCAGAGCAATTTC | 55120 |
rs149941247 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58202878 | ATGAGGACAGGGTGT[A/G]TTTAAAATCTTTAGT | 55120 |
rs149974680 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FANCL | GRCh38.p7 | 2:58220855 | CCTCGATTTATCTTA[A/G]TAATAGGGCAATCTA | 55120 |
rs149995807 | snp | C/T | 0.000798403 | 0.0199641 | downstream-variant-500B, intron-variant | FANCL, VRK2 | GRCh38.p7 | 2:58158815 | TAATATCTATTCGGT[C/T]TATACTGGTTCGTCT | 55120 |
rs150023740 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58186206 | CTTAGGAGGTCATAT[A/G]TAATTGCATAGGTTT | 55120 |
rs150089848 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | FANCL | GRCh38.p7 | 2:58198274 | GTTGGCCCTACCCAC[A/G]GATTCCACATGTGCA | 55120 |
rs150130711 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228338 | ACAATGCATGAACAC[A/G]TATGATTCACATCTT | 55120 |
rs150218524 | snp | G/T | 0.180383 | 0.240111 | intron-variant | FANCL | GRCh38.p7 | 2:58174991 | CAAACTACCATCAGA[G/T]AATACTATAAACACC | 55120 |
rs150241527 | in-del | -/C | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58229214 | GCATAAAAAGAAAGG[-/C]AATTCTAAAAACTAT | 55120 |
rs150246372 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58205345 | AATCTGTAGAAAGTC[G/T]AGGGTCTTAGAAAAC | 55120 |
rs150298520 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58239712 | GTATTTAGGGATAAA[G/T]GGGAACTACGCCTGA | 55120 |
rs150352205 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58232570 | TTCTAAATTTTAATA[A/T]AATGAAAATATATTT | 55120 |
rs150384673 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58222251 | TCATGCAAAATGTCA[A/G]TTTTTATGCCATGAA | 55120 |
rs150405034 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58171913 | CACCCCAATACTGCG[C/G]TTTTCCGACGGGTTT | 55120 |
rs150427970 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58212444 | ACAGAACCAAACCAT[A/G]TCATAAAGTGATATG | 55120 |
rs150459180 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | FANCL | GRCh38.p7 | 2:58167083 | TGGGCGTAGTGGCAC[A/G]CGCCCATAGTCCCAG | 55120 |
rs150477517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179198 | ATCCCCATCAATCTA[C/T]CACTGGCTTTCTTAA | 55120 |
rs150545505 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58190165 | TCTGGTCAAACACTG[G/T]TATCTGTCAAGCAAT | 55120 |
rs150567751 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58207010 | CCCACTCAACTCTCA[A/G]TAAAACCAAGTTTTA | 55120 |
rs150586924 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58217489 | ACAGCATTAAAATCT[G/T]TTTTAAAAAAATGCA | 55120 |
rs150620578 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242190 | GAGCAAAGATTATTT[C/T]GTCCCCTACCCATCT | 55120 |
rs150701382 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58195564 | CAGAAACCACAAGAG[A/G]AGGATGTGACCAGAC | 55120 |
rs150735157 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | FANCL | GRCh38.p7 | 2:58214066 | GAAATAAAAATATTT[A/G]TCCTAAAATTTATCC | 55120 |
rs150752804 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | FANCL | GRCh38.p7 | 2:58230297 | ATAACTAAAAGGATA[A/C]ATTTTATTTTTATTT | 55120 |
rs150772160 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | FANCL | GRCh38.p7 | 2:58170355 | AGATCTTGTCACCAC[C/G]AGGCCTGCCTTACAA | 55120 |
rs150796502 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FANCL | GRCh38.p7 | 2:58180099 | GAGGATGTGGAGAAA[C/T]AGGAATGCTTTGACA | 55120 |
rs150830596 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58201568 | CCCACCCTCTGATGC[A/G]TATATGTAATTTGTT | 55120 |
rs150954346 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | FANCL | GRCh38.p7 | 2:58178239 | ACTCATTTTATGAGG[C/G]CTGCATCATCCTGAC | 55120 |
rs151009591 | snp | A/C | 0.0103295 | 0.0711199 | intron-variant | FANCL | GRCh38.p7 | 2:58179637 | CATAAAAACCCTAGA[A/C]GAAAACCTAGGCAAA | 55120 |
rs151023033 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58197952 | TTCTTTGGAATTTAA[A/T]TTTAAAGGAAAATGT | 55120 |
rs151051705 | snp | C/G | 0.0130921 | 0.0798413 | intron-variant | FANCL | GRCh38.p7 | 2:58187280 | GGGACACGGATGAAG[C/G]TGGAAACTATCATTC | 55120 |
rs151075064 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58232205 | AAAAGACAATGTTTT[C/G]CTTTATTTTCTAAAA | 55120 |
rs151149443 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58172540 | ACCTGCAGCTGAGGG[C/T]CTCTGTTAACAGAGG | 55120 |
rs151181785 | snp | C/T | 0.000760481 | 0.0194849 | synonymous-codon, nc-transcript-variant | FANCL | GRCh38.p7 | 2:58198600 | AGAATTTACCTGAGG[C/T]GTCCAGGAGGCACAA | 55120 |
rs151228630 | snp | C/T | 8.31954e-05 | 0.00644909 | intron-variant, utr-variant-3-prime, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58161476 | CAGGAATACTTCCTA[C/T]GTTGTGTTAGCGGAA | 55120 |
rs151232851 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | FANCL | GRCh38.p7 | 2:58239416 | AAATTGAGATACATT[C/T]TACCTAACAGCCAAT | 55120 |
rs151281379 | snp | A/T | 0.0236746 | 0.106192 | intron-variant | FANCL | GRCh38.p7 | 2:58191986 | AGAGCCAGAATTTGA[A/T]CCAGACTTTAAGACT | 55120 |
rs151296511 | snp | C/G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58208751 | ACTAGAAACAATCTT[C/G/T]CTAATGCGTGTCTTT | 55120 |
rs151315563 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | FANCL | GRCh38.p7 | 2:58220088 | TACAGAGACTTTAAG[C/T]AGTCCATCTGCAGTG | 55120 |
rs180718606 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239132 | CGTGATAGTAATAGT[C/G]GACTCAAGCAAAAGT | 55120 |
rs180720762 | snp | G/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58221401 | ACAACTTGCATACAC[G/T]TTTACTGAACTTAAG | 55120 |
rs180733074 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58205185 | TTAATATCACTATAT[G/T]CCATTTAGATACTGA | 55120 |
rs180742448 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230288 | CCGATTAATATAACT[A/G]AAAGGATACATTTTA | 55120 |
rs180745738 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58187601 | GCAAAGAAAGTGAAG[C/T]TGGAAGCAAGAATTA | 55120 |
rs180746395 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58212138 | AGAAAGAGGTTTAAT[C/T]GGACTTACAGTTCCA | 55120 |
rs180755620 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58195070 | AAATCTAACTCTGCT[A/G]TTAAACTACAACAGT | 55120 |
rs180765858 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58181780 | ATAAAACATTGGAGG[G/T]GGGAATGAATCTCAA | 55120 |
rs180829286 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58165377 | TGAGAAGATTGTAAG[A/C]TTCACAAATGAAGAC | 55120 |
rs180829785 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58172727 | CTCTAAAAAGCAGAG[C/T]GCCTCTCCTCCTCCA | 55120 |
rs180872793 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58191051 | CAGAAATGAAGGTTT[A/G]AAACTTATAAACACA | 55120 |
rs180907124 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58208725 | AGCATTAACTACTTC[A/G]TATCTGGATTACTAG | 55120 |
rs180924541 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58178734 | AAGTTCTAGCCAGGG[C/G]AATCAGGCAAGAGAA | 55120 |
rs180959380 | snp | G/T | 0.030665 | 0.119967 | intron-variant | FANCL | GRCh38.p7 | 2:58169672 | AAAAAGTTAGAGGAA[G/T]TGCTAACTAAAATAA | 55120 |
rs181011049 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58161938 | GTATTATAGGAAATA[C/T]AATTACATTACTATT | 55120 |
rs181116852 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58172133 | CACCACAGCTCAAAG[A/C]GGCCTGCCTGCCTCT | 55120 |
rs181125107 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58166437 | TGATGTTTTTCCACA[A/T]TTAACTTTTAGCCAA | 55120 |
rs181267588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58230735 | TCATTCAAATGTCCA[C/T]TGGTAACCCCTGCTC | 55120 |
rs181365306 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | FANCL | GRCh38.p7 | 2:58213187 | AGATTCTGTAAATAC[A/C]TTTAAATCAATCTGT | 55120 |
rs181368637 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241916 | ACTCAGTTCTGTGTA[C/T]GGCACTCACAAATAT | 55120 |
rs181369414 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58226138 | GAGGAAATAAGATTG[G/T]CAAAATGTTAAAATT | 55120 |
rs181378422 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58209615 | AACTAGTATCTCAAC[A/G]ACTTGATACACCTAC | 55120 |
rs181383566 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58191596 | TTTCATTTTTGAGCA[C/T]AGAAAACTCCTTGTT | 55120 |
rs181388361 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58179028 | TCCAACTTACAAGGG[A/C]TGTGAAGGACCTCTT | 55120 |
rs181430705 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58184688 | GCTGCATGCCCCAAA[A/C]GCAATAAACTGTCTT | 55120 |
rs181434409 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | FANCL | GRCh38.p7 | 2:58185038 | AAGAGGCACAGGCCA[A/G]ACAAGAGAAACTAGA | 55120 |
rs181458905 | snp | A/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242357 | TCAAAACGTGATCCT[A/G]GAACCTAGCAACAGC | 55120 |
rs181472674 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58226980 | ACAGTAATTAATGTC[C/G]TCAAATCTAATTTGC | 55120 |
rs181474334 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58210310 | AGTCCCATCTTACAC[A/G]GATGGCAGCAAAGAC | 55120 |
rs181495324 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58216717 | CAAAAAAGTGAAAAC[A/G]GAATGCACACTGTCC | 55120 |
rs181502442 | snp | A/G | 0.00101342 | 0.0224873 | intron-variant, downstream-variant-500B, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160213 | AAAGGAGAAGCGTCA[A/G]CATGATTACAAATTA | 55120 |
rs181512994 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58234830 | AATAGAAAATGTTAA[G/T]AAACTGAAGAGAACT | 55120 |
rs181526368 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58200628 | TAAAGTATCTGTGGC[A/C]CCATTAAGTACATAC | 55120 |
rs181559297 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58200108 | TCTACTTCTGGAAAA[A/C]AAAAAAAAGAAAAAA | 55120 |
rs181630882 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58172343 | GCAGCCTAACTGGGA[A/G]GCACCGCCCAGTAGG | 55120 |
rs181652262 | snp | C/T | 0.00119832 | 0.0244484 | intron-variant | FANCL | GRCh38.p7 | 2:58218315 | AGCAGATATTAATGA[C/T]AAAAAAATATACAAC | 55120 |
rs181706802 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58169928 | CAAACCTATGTTTGA[C/T]TGGTGTGCCTGAAAG | 55120 |
rs181723539 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | FANCL | GRCh38.p7 | 2:58196076 | TATTTAAAATAAATA[C/T]AGTAGACAAACATAA | 55120 |
rs181769508 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58170232 | GTGGGGGCCAATATT[C/T]AATATTCTTAAAGAA | 55120 |
rs181852038 | snp | A/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58234981 | TCCTTGAAATAAGGG[A/G]AACAAATGTGAAAAT | 55120 |
rs181862205 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | FANCL | GRCh38.p7 | 2:58218898 | ATATAAATGGTTATA[C/T]ACAAAAACATTTACA | 55120 |
rs181868007 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58201290 | ATATAGGAATATTAA[C/G]TGAAAAATAAGTATA | 55120 |
rs181873650 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58185802 | CAGGAGATAAACAAA[A/G]ATTCTGTTAGTTCCA | 55120 |
rs181933795 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58182049 | ATAATCTTTGAAATG[A/C/T]CTATGATAAGCATTC | 55120 |
rs181945748 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58160515 | AGTTCCTGGCATTCA[C/T]AGACTTTCCCTAAAT | 55120 |
rs181979078 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58237660 | ATTTATAAACCTCTA[A/T]CTAGATGTATCGGGG | 55120 |
rs181983515 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58221008 | ACGAGGTCAGGAGAT[A/C]GAGACCGATCCTGGC | 55120 |
rs181986608 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | FANCL | GRCh38.p7 | 2:58182862 | TATGCTGATTAAGAT[A/C]AAAAACTATAGTCAA | 55120 |
rs181997869 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | FANCL | GRCh38.p7 | 2:58187427 | TCGTGGGGTGGGGGG[C/G]ATGGGGAAGGGATAG | 55120 |
rs182066902 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58231964 | AGCATTTTAGGCAAA[A/C]CTCTAGTCACTAGAA | 55120 |
rs182067066 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58214992 | GATCCACTGAGGTAG[C/G]CTGCCTCAAACTCAC | 55120 |
rs182075991 | snp | C/G | 0.0217236 | 0.101931 | intron-variant | FANCL | GRCh38.p7 | 2:58197140 | TCAACTTCCATTGTG[C/G]GGAGATTGGGACTTT | 55120 |
rs182084060 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58183111 | AGCCTAATGAAACAA[C/T]AGCAAAATATCTGTA | 55120 |
rs182101791 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | FANCL | GRCh38.p7 | 2:58225958 | ACAAACAAAGCAGCT[A/G]TAAGAAATTATTAAC | 55120 |
rs182231639 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58213559 | AATGATTAAGTAACA[C/G]CAGCTAAATCGAAAG | 55120 |
rs182314097 | snp | C/G | | | intron-variant | FANCL | GRCh38.p7 | 2:58170431 | CAGCCACTGCAAAAA[C/G]ATACGAAAATGTAAA | 55120 |
rs182323984 | snp | A/T | | | intron-variant, downstream-variant-500B | FANCL, VRK2 | GRCh38.p7 | 2:58164183 | GACTACAGCGTAAGT[A/T]TCAGAAATTTTACTT | 55120 |
rs182350291 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58240506 | TCCGGTTTCCCATAC[C/T]TTGATTTCTTCAACT | 55120 |
rs182368226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206855 | TACATTTTACCCATG[C/T]TGCTTCCTGGTCACT | 55120 |
rs182391604 | snp | C/T | | | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58241502 | TGCGGGAGGCGACAT[C/T]AGGGCTCCCCAACCG | 55120 |
rs182431723 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | FANCL | GRCh38.p7 | 2:58168527 | CTGGGTGGTCATTTG[G/T]GCAGACATTGAGCTA | 55120 |
rs182487795 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58231633 | TCCTGACTAGTTGTA[C/T]CTACCAGCACTCAAT | 55120 |
rs182508484 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58196667 | TCACAAACTGATTTT[C/G]TTAAATAACAAAATA | 55120 |
rs182593669 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | FANCL | GRCh38.p7 | 2:58242934 | TAGGGCTCAGCAGTC[C/T]GCGTTTTAACAAGCT | 55120 |
rs182595690 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58228660 | AGAAAAAGTCTGTTG[A/C]CTCCCTGGCCCATAT | 55120 |
rs182605434 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58210890 | TCCCATGACCTTGGG[G/T]AGCTAGACCCCTGTG | 55120 |
rs182610168 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58222831 | TCTGAAGTATCAAAC[A/G]GTATTACAAAAAGTA | 55120 |
rs182612852 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58193399 | CTTCTTTTTTAGAAT[C/T]AATATAGGCTGCTTT | 55120 |
rs182623614 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58180426 | CCTTTGCAGGGACAC[A/G]GATGAAGCTAGAAAC | 55120 |
rs182635834 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | FANCL | GRCh38.p7 | 2:58189949 | TTCTTTATCTTTGGG[A/G]GATTCCAAAAGTATA | 55120 |
rs182656833 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | FANCL | GRCh38.p7 | 2:58221640 | GTGTCTCAGCATTAC[G/T]CTTCAAACATGGAAA | 55120 |
rs182664995 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58206003 | AGAATACGCAATGCT[A/G]AAAGACTTAATTATA | 55120 |
rs182670062 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58187830 | TTGAGAGTTCTTTAT[A/G/T]TATTTTAAACACATC | 55120 |
rs182680821 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | FANCL | GRCh38.p7 | 2:58175554 | GATTATCTCAATAGA[C/T]GCAGATAAGGCCTTT | 55120 |
rs182731100 | snp | C/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58177757 | TGCACATTGTGCACA[C/T]GTACACTAAAACTTA | 55120 |
rs182883988 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58202692 | TCTACCTTGAAAAAG[C/T]ATAGAAAAAAGCAGA | 55120 |
rs182888427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58186407 | AGAAGGCAAAGCCAG[A/G]GACAAGGACATGTAT | 55120 |
rs182937474 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58232611 | TCTATACAGACATAA[C/G]TGAAATACTTGCATA | 55120 |
rs182961891 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58198227 | AGATTACTTCATAAC[C/G]TATAATGACTACCTA | 55120 |
rs183021299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58170817 | TCAATGCAACAAGGA[G/T]AGCTAACAATCCTAA | 55120 |
rs183036287 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant, utr-variant-3-prime | FANCL, VRK2 | GRCh38.p7 | 2:58162451 | AAGTATATAGTTGAC[C/G]CTTGAACAACATGGG | 55120 |
rs183111468 | snp | A/C | | | intron-variant | FANCL | GRCh38.p7 | 2:58219204 | TATATATATATATAT[A/C]TCCACAATGATGAGG | 55120 |
rs183122859 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | FANCL | GRCh38.p7 | 2:58185949 | CCTATCACTGAAATA[C/T]TGAGAAACACTTACA | 55120 |
rs183144578 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | FANCL | GRCh38.p7 | 2:58173042 | AAGGGTATCAGTGAC[A/G]GAAGATGAAGTGAAT | 55120 |
rs183167080 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58173263 | CAAGGCAGGCCAACA[A/T]TCAGATTAAAGAAAT | 55120 |
rs183227822 | snp | A/T | | | intron-variant | FANCL | GRCh38.p7 | 2:58215664 | GCAAGAGAAGAAGGA[A/T]CTGGGCAAAGAGCCC | 55120 |
rs183232217 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58239574 | CATACAACTGTATCA[C/T]AAACAAAATTTGAAA | 55120 |
rs183241222 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | FANCL | GRCh38.p7 | 2:58168232 | GGCAGGTGATTTCTG[C/T]ATTTCCAACCAAGGT | 55120 |
rs183243430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | FANCL | GRCh38.p7 | 2:58235482 | GCAATGCTTAAAAGC[C/T]TAAAGCTTAAAATTA | 55120 |
rs183251765 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | FANCL | GRCh38.p7 | 2:58183429 | TTGGCTCCTCTCTTA[C/T]AGCACTCCCCTTATT | 55120 |
rs183300146 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | FANCL | GRCh38.p7 | 2:58179194 | TGCTATCCCCATCAA[G/T]CTACCACTGGCTTTC | 55120 |