SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs724909 | snp | A/C | 0.483995 | 0.0880135 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929928 | AGTAAAAACTGTTTC[A/C]ATTTTTGACTGTGTT | 9169 |
rs735351 | snp | A/T | 0.417683 | 0.185425 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935409 | AGGCTGAGTTCCGGA[A/T]CTTACTGCCTTACCC | 9169 |
rs764192 | snp | A/C | 0.193966 | 0.243639 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969244 | ACTTCTGATTCCCCG[A/C]GGCTTGAGGTACCCA | 9169 |
rs997307 | snp | A/G | 0.474634 | 0.109726 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953341 | TATGAAATTTCTTAA[A/G]AGATTATATTAATGC | 9169 |
rs997308 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953538 | AACAGAGTGAGATCC[C/T]ATCTCTGAAACATAG | 9169 |
rs1012642 | snp | C/T | 0.472147 | 0.114677 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959496 | TTAGAAGGCTGAAGA[C/T]ACTTATTCCTGATCC | 9169 |
rs1047878 | snp | A/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921265 | gccgggcatgatggc[A/T]cacgcctgtaatccc | 9169 |
rs1062905 | snp | A/T | 0.417683 | 0.185425 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923221 | TTAATGTTATTTCTA[A/T]TGCATCACTAAAAGA | 9169 |
rs1291620 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941841 | gggtctgcttattca[C/T]gaatgtttttcaata | 9169 |
rs1291621 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947038 | GTGTTATAAATTAGT[A/G]ATAGGTTGAATTAAT | 9169 |
rs1291622 | snp | C/G | 0.0119091 | 0.0762411 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951300 | CTAGCCAATTAAATT[C/G]TTTGAAATATGGGAA | 9169 |
rs1291623 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955636 | TTAACTAATACTTAC[A/T]CTATTTTTAAGTTAT | 9169 |
rs1291624 | snp | C/G/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972881 | ATATATATATATATA[C/G/T]ATATATATATAGATA | 9169 |
rs1291626 | snp | C/T | 0 | 0 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921655 | AAAGATCATACTTTA[C/T]ATTTTAACCTGACAG | 9169 |
rs1291627 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932636 | TTAAGTATATATTAT[A/T]TATCTAGCACCATCT | 9169 |
rs1291628 | snp | G/T | 0.188 | 0.24219 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932793 | AAAGCGTGATTCAGC[G/T]GACAGCACGCAGGTA | 9169 |
rs1366023 | snp | C/T | 0.193028 | 0.243422 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986378 | GAGACCAGCAGGCCT[C/T]AGTTAATAGATTGAA | 9169 |
rs1366024 | snp | A/G | 0.469049 | 0.120489 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919855 | AACTTGTTTGCAAAA[A/G]CTAAATGGTATAAAA | 9169 |
rs1427749 | snp | C/G | 0.215446 | 0.2476 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976333 | acagtaagatatttt[C/G]agagagcccacattc | 9169 |
rs1549591 | snp | G/T | 0.209388 | 0.246679 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993430 | CCTTAATTTGAACTT[G/T]ATATTGTATTCTATT | 9169 |
rs1802104 | snp | C/T | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926827 | ATTTGGTAGAATTGA[C/T]AGAGATAGTTACTCT | 9169 |
rs1978598 | snp | C/G | 0.200182 | 0.244986 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984023 | CTTTTAAAGTTTATA[C/G]TTATTCCTTTTTGTA | 9169 |
rs2022104 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972557 | ttgctgtcgcatcca[A/G]gctgaagtgcatggc | 9169 |
rs2408438 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935894 | TTTCCTGAAGATCGT[C/T]TCACAAATCCACCCT | 9169 |
rs2408439 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935895 | TTCCTGAAGATCGTT[C/T]CACAAATCCACCCTA | 9169 |
rs2408440 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935896 | TCCTGAAGATCGTTT[C/T]ACAAATCCACCCTAC | 9169 |
rs2408441 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935897 | CCTGAAGATCGTTTC[A/G]CAAATCCACCCTACT | 9169 |
rs2408442 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935900 | GAAGATCGTTTCACA[A/G]ATCCACCCTACTTGT | 9169 |
rs2897932 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935898 | CTGAAGATCGTTTCA[A/C]AAATCCACCCTACTT | 9169 |
rs4144983 | snp | A/G | 0.406468 | 0.194981 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976284 | TCAACGTCTTGTGTC[A/G]TTCCACCTTCATTTC | 9169 |
rs4768099 | snp | G/T | 0.204803 | 0.245881 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958639 | TGAATTCCTTGAAAC[G/T]AAATATAATCATAGT | 9169 |
rs4768100 | snp | A/T | 0.417034 | 0.18601 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965191 | ATAAGTGAATTTTTT[A/T]AAAAAAGATAGATAC | 9169 |
rs4768670 | snp | G/T | 0.418169 | 0.184985 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948084 | TTTAATTCTTTTTAT[G/T]TTGTGTTATTTTTTA | 9169 |
rs4768671 | snp | C/T | 0.215446 | 0.2476 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958780 | GGATTCTGACATACC[C/T]AAAGACTTTTTACTT | 9169 |
rs5797955 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969229 | ATTTTAACAGTTGCT[-/T]GGGTACCTCAAGCCT | 9169 |
rs5797956 | in-del | -/A | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993793 | CAAAAAAAAAAAAAA[-/A]GAAAAAGAAAAAAAA | 9169 |
rs6582578 | snp | C/T | 0.19459 | 0.243782 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941341 | taatgttctgatata[C/T]gtacacattgtgaaa | 9169 |
rs6582580 | snp | A/T | 0.253264 | 0.249979 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987945 | GTCTATGTACTAGGA[A/T]TTCATACATTAAGTT | 9169 |
rs7298703 | snp | C/G | 0.482609 | 0.0916147 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957610 | ATTTTATACAAAATG[C/G]GTGATTTTGTATAAA | 9169 |
rs7306229 | snp | C/T | 0.474091 | 0.11083 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941049 | TTAGTCTTAAACATT[C/T]TGCCTGAACTCAAGA | 9169 |
rs7309711 | snp | C/T | 0.189261 | 0.242509 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932499 | GTTCTGCCATCATTC[C/T]TAGAGGGTGAATGCC | 9169 |
rs7315715 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961347 | ATAAAACAAAAAGCA[A/G]ACAGAAGGTGTTATT | 9169 |
rs7315731 | snp | A/T | 0.49644 | 0.0420383 | missense | SCAF11 | GRCh38.p7 | 12:45927731 | TCTTGAATATTATTG[A/T]AATCTTCATTCCCAA | 9169 |
rs7964761 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952109 | ATTTTAATATTCTAT[C/G]ACTTAATATTTTCCC | 9169 |
rs7965539 | snp | A/T | 0.192088 | 0.2432 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935781 | ATCCAGTTCAAAAGC[A/T]GTTTCACATATTTCT | 9169 |
rs7967208 | snp | A/G | 0.493568 | 0.0563433 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954293 | ctggagtgcagtggc[A/G]ctatcatgggtcact | 9169 |
rs7968005 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948779 | CTTATAACAGAGATA[C/T]GAACACAGATTTGTA | 9169 |
rs7968469 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958138 | ttaaactcctgggct[C/T]gagtgatccaccctc | 9169 |
rs7971936 | snp | G/T | 0.253264 | 0.249979 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959342 | TAAAAAGATTTTAAC[G/T]TCAGGCTATCCCTTG | 9169 |
rs7972499 | snp | G/T | 0.19459 | 0.243782 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987482 | GCTGATCTCACAGAA[G/T]ATAAATCACAGTGAA | 9169 |
rs7973329 | snp | C/T | 0.215446 | 0.2476 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987423 | ATTCATTAACTTACA[C/T]TGAAGGCATTGTTCA | 9169 |
rs10492249 | snp | C/T | 0.0150606 | 0.0854603 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45919033 | CCATGATGCGAATGA[C/T]TGGTACAAATCCAAG | 9169 |
rs10506264 | snp | C/T | 0.194902 | 0.243853 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957866 | TTTTTAATCACTTCT[C/T]GGCAACTGTGGGAAA | 9169 |
rs10683271 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972901 | atatatagatatata[G/T]atatatagatatata | 9169 |
rs10785592 | snp | A/G | 0.475081 | 0.108804 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984158 | TTACCTTAATAAAAA[A/G]AAAAAGGGATTACTT | 9169 |
rs10785593 | snp | C/T | 0.46865 | 0.121211 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990241 | ATTCCGAAACTTTGT[C/T]AGCCCTCGCGTCGCC | 9169 |
rs10785594 | snp | C/T | 0.468349 | 0.121752 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990247 | AAACTTTGTCAGCCC[C/T]CGCGTCGCCCTAGGC | 9169 |
rs10785595 | snp | C/T | 0.46865 | 0.121211 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990248 | AACTTTGTCAGCCCT[C/T]GCGTCGCCCTAGGCC | 9169 |
rs10880867 | snp | A/G | 0.418007 | 0.185132 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920609 | AGTATTAAAAAGAGA[A/G]AAAAAAAAAAACCCA | 9169 |
rs10880868 | snp | C/T | 0.284619 | 0.247591 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928666 | ACCTGGGGCATCACA[C/T]CCAGAATTGTCTGAT | 9169 |
rs10880869 | snp | C/T | 0.147321 | 0.227941 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932365 | CAATATAAGGTAAGA[C/T]TCTGGAGTAGGAGAA | 9169 |
rs10880870 | snp | C/T | 0.11275 | 0.208956 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944297 | TTTAACCACAGAAGT[C/T]CAGAGATCAAAACAA | 9169 |
rs10880871 | snp | C/G | 0.47023 | 0.118317 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946955 | TCTAGCAGAAGGGAT[C/G]TGAATCATTCTTCAC | 9169 |
rs10880872 | snp | C/T | 0.197703 | 0.244469 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951196 | CACAGTTTTCAGTTA[C/T]TTTGGACTTAAGGTT | 9169 |
rs10880873 | snp | C/T | 0.416871 | 0.186156 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966041 | GGAATATTTCCCACT[C/T]TTAGCCTATGTGTGC | 9169 |
rs10880874 | snp | A/T | 0.416871 | 0.186156 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966049 | TCCCACTCTTAGCCT[A/T]TGTGTGCAACATTAG | 9169 |
rs10880875 | snp | C/T | 0.470618 | 0.117591 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967236 | AAAAAAAAAACAACC[C/T]ACAATTAATATTTTA | 9169 |
rs10880876 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972914 | TATATATATAGATAT[A/C]TATATAGATATATAG | 9169 |
rs10880877 | snp | G/T | 0.0807149 | 0.183963 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972921 | ATAGATATATATATA[G/T]ATATATAGATATATA | 9169 |
rs10880878 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972929 | ATATATAGATATATA[G/T]ATATATATAGATATA | 9169 |
rs10880879 | snp | C/T | 0.483199 | 0.0901004 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974120 | GTATATATGTTTATA[C/T]TATACTGTAGTCCAT | 9169 |
rs10880880 | snp | A/G | 0.470618 | 0.117591 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981523 | TTCTCCCATTTTCTG[A/G]GGAATAAATATAATC | 9169 |
rs10880881 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985299 | TTGATCAACCCCCTG[C/T]ATGTGGCCAGTTTCC | 9169 |
rs11183237 | snp | A/T | 0.0107246 | 0.0724382 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920014 | GCACACCTCCTTAGT[A/T]GTTTTAGATTAGAAC | 9169 |
rs11183240 | snp | A/C | 0.0460142 | 0.144533 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932291 | CATTCAAACCCAAAC[A/C]ACTTCTTGGCTTTCT | 9169 |
rs11183241 | snp | C/T | 0.493154 | 0.0581045 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936415 | CCAAAGTGCTGGGAT[C/T]ACAGGCATGAGCCAC | 9169 |
rs11183242 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938357 | AGCCGGGCATGATGG[C/T]GGGCACCTGTAATCC | 9169 |
rs11183243 | snp | A/G | 0.474634 | 0.109726 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942475 | AATGTACCAGATCAC[A/G]TTACTCCTGAAAACA | 9169 |
rs11183244 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944976 | AATAAGGCCACAGTA[C/T]GAGCTGGTCAACACC | 9169 |
rs11183245 | snp | C/T | 0.0078325 | 0.0620878 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45945250 | CTTGAAGTGGATACA[C/T]AGTAAGTTACTTTTT | 9169 |
rs11183246 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954769 | TTAACTTTTTTCATA[A/G]AGACAGGGTCTCACT | 9169 |
rs11183247 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959776 | AATTTATTAATAGAT[G/T]GCTCTCTTGTTACTG | 9169 |
rs11183248 | snp | A/G | 0.195214 | 0.243923 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45960850 | ATTAGCTGCATTCCA[A/G]TTGTTAATGTTCTTA | 9169 |
rs11183249 | snp | C/T | 0.0463947 | 0.145069 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961154 | ACAggaattagaaaa[C/T]cagttctaaattcac | 9169 |
rs11183250 | snp | A/T | 0.0460142 | 0.144533 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961483 | TTATTAACTTTTTTT[A/T]AAAAAGTATGCATTT | 9169 |
rs11183251 | snp | A/G | 0.406296 | 0.19512 | intron-variant | SCAF11 | GRCh38.p7 | 12:45962868 | TGATAAATTAAATCT[A/G]TGAGGGCCTAATTTA | 9169 |
rs11183253 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968255 | ATTTTCAGTAAACTT[C/T]GCTTTTCTGATTATT | 9169 |
rs11183254 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972856 | AAAGCCAGTATATAT[A/C]TATATATCGATATAT | 9169 |
rs11183255 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972857 | AAGCCAGTATATATA[G/T]ATATATCGATATATA | 9169 |
rs11183256 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972864 | TATATATATATATAT[A/C]GATATATATATATAT | 9169 |
rs11183257 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972865 | ATATATATATATATC[G/T]ATATATATATATATA | 9169 |
rs11183258 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972873 | ATATATCGATATATA[G/T]ATATATAGATATATA | 9169 |
rs11183259 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972885 | ATATATATATAGATA[G/T]ATATATAGATATATA | 9169 |
rs11183260 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972893 | ATAGATATATATATA[G/T]ATATATATATATATA | 9169 |
rs11183261 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972903 | ATATAGATATATATA[G/T]ATATAGATATATATA | 9169 |
rs11183262 | snp | G/T | 0.444444 | 0.157135 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972915 | ATATATATAGATATA[G/T]ATATAGATATATAGA | 9169 |
rs11183263 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972919 | ATATAGATATATATA[G/T]AGATATATAGATATA | 9169 |
rs11183264 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972923 | AGATATATATATAGA[G/T]ATATAGATATATATA | 9169 |
rs11183265 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972931 | ATATAGATATATAGA[G/T]ATATATAGATATATA | 9169 |
rs11183266 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972935 | AGATATATAGATATA[G/T]ATAGATATATATATA | 9169 |
rs11183267 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972943 | AGATATATATAGATA[G/T]ATATATAGATATATA | 9169 |
rs11183268 | snp | G/T | 0.499819 | 0.00950293 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974156 | GTGCAACAGCATTAT[G/T]TCTAAAAACTGTACA | 9169 |
rs11183269 | snp | A/G | 0.422341 | 0.181103 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974161 | ACAGCATTATGTCTA[A/G]AAACTGTACATACTT | 9169 |
rs11183270 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974318 | GTAGTTGCTGAAGGG[A/C]AGGGTTGGCTGTGGC | 9169 |
rs11183271 | snp | C/T | 0.0460142 | 0.144533 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987644 | AGAAGACCACAACAG[C/T]GTAGGGGAAAGGAGA | 9169 |
rs11183272 | snp | A/C | 0.497558 | 0.0348586 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988473 | AAAGCACAGGTTTTC[A/C]AGAAAACTGTCTAAG | 9169 |
rs11183273 | snp | A/T | 0.434976 | 0.168179 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993318 | TCCTGTCACATAGCA[A/T]CAGAAACCCACAGTG | 9169 |
rs11348395 | in-del | -/A | 0.072874 | 0.176427 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945218 | AAACAACAAAAAAAA[-/A]GGTAGAATCCACAAG | 9169 |
rs11503846 | snp | A/T | 0.375 | 0.216506 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979889 | TGCAAACTTAAAATT[A/T]AAAAAAAAAAAATTC | 9169 |
rs11545903 | snp | A/G | | | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990375 | GGCCGCGGCCGGACC[A/G]AGCGCCTCGACCTCG | 9169 |
rs11574952 | snp | A/G | 0.437611 | 0.165234 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45992032 | AGGCGGCAGTGAAGC[A/G]GTCGGTCGGCGGGGC | 9169 |
rs11574953 | snp | C/T | 0.0123036 | 0.0774623 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991206 | AGGCGGGAAAGCTCT[C/T]CCCCTGGCATCTAAA | 9169 |
rs11574955 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990902 | CGCATGCGCACCATC[C/T]GCAGTGTGGGCGAAG | 9169 |
rs11574956 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989398 | ACATTTTGGCTAACA[C/T]GCTACCACTGACCTA | 9169 |
rs11574957 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965489 | CCATCTCTTAGGAAA[A/G]AAAGTTGATTAAAAT | 9169 |
rs11574958 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963571 | CTGAGAAGTTTCTTT[A/G]GTGAAGGTCTATTGG | 9169 |
rs11574959 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962115 | AGAAATTTGCTCTTA[A/T]ATTTTTGATCCGTGT | 9169 |
rs11574960 | snp | A/C | 0.109814 | 0.206997 | intron-variant | SCAF11 | GRCh38.p7 | 12:45960076 | CTTGTCTATATTTTT[A/C]ACTCTTGTTGAATAT | 9169 |
rs11574961 | snp | A/G | 0.0240643 | 0.107019 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952593 | GAAATAAAGCAAGAT[A/G]ATGTTGACTTATAAT | 9169 |
rs11574962 | snp | C/T | 0.0704125 | 0.17392 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951474 | ACTTAAATTCTGAAC[C/T]TTTTATTCATTTGCC | 9169 |
rs11574963 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951367 | ACGTTTTGTACTAAG[A/G]CTTAATTATAAAATA | 9169 |
rs11574964 | snp | A/C | 0.224412 | 0.248687 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950932 | AATGAAAAATAGCTA[A/C]AAATGAGAGTACTCA | 9169 |
rs11574965 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950745 | ATAATTTGTTTTGAT[A/G]TATTTTTACCAGATG | 9169 |
rs11574966 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948635 | ACTTTTTAATTGGAC[A/G]GTTTTGTTTCTGTAA | 9169 |
rs11574967 | snp | A/C | 0.00636936 | 0.0560724 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948621 | CAGTTTTGTTTCTGT[A/C]ATTTTAATCATTTCA | 9169 |
rs11574968 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935392 | CCGGAACTCAGCCTG[G/T]TCGTCTTCCACTAAC | 9169 |
rs11574969 | snp | A/G | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935265 | AGTAGAAAGTAGGCT[A/G]TTACCAACTGAACTA | 9169 |
rs11574970 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934005 | TAGCTCTAGCAAAGA[G/T]AAAACCTGTTAATTT | 9169 |
rs11574971 | snp | C/T | 0.0656767 | 0.168893 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927634 | GAATGAATCGCTGAC[C/T]GAACATCCTAGATCT | 9169 |
rs11574972 | snp | A/G | 0.000412123 | 0.0143489 | missense | SCAF11 | GRCh38.p7 | 12:45927173 | AGTCAGCCAGAGGCC[A/G]GAAAAAATCCCGTTC | 9169 |
rs11574973 | snp | A/C/G | 0.00440834 | 0.0467418 | missense | SCAF11 | GRCh38.p7 | 12:45924853 | CATCTCCACACAGGA[A/C/G]TGCCCCTCATGCAGG | 9169 |
rs11574974 | snp | A/G | 0.0146672 | 0.084371 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922300 | ATAATGAAACATGAA[A/G]ATAAGTCTGGTTATC | 9169 |
rs11614588 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986683 | tattcccataattcc[A/C]acgtgttgtgggagc | 9169 |
rs11829302 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972036 | gtaacagctgttttt[A/G]aactcctaactcacc | 9169 |
rs11838294 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964886 | TAACATTTAGCTAGG[C/T]CAATCTCACAATTGA | 9169 |
rs12049947 | snp | A/G | 0 | 0 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993286 | TGTTGCACTTTACCA[A/G]GCACTTAAAATATCA | 9169 |
rs12229821 | snp | G/T | 0 | 0 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920861 | GTCTTGTAATTCTTA[G/T]CCCCAAGGAAGGGAG | 9169 |
rs12297051 | snp | A/T | 0.0532157 | 0.154195 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985650 | accgaaaagatcaaa[A/T]gaaaatgtatgtaaa | 9169 |
rs12297909 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955217 | caggctgtagtgcag[C/T]ggcatcacggctcac | 9169 |
rs12298353 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950091 | GGATGTTTTAGAAGC[C/T]GAAGGAATTAGAGGG | 9169 |
rs12301327 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947707 | tttgagacagagtct[A/T]gctctgttgctcagg | 9169 |
rs12307626 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948213 | actgggattatagga[C/G]tgagccaccatgccc | 9169 |
rs12309561 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949306 | tggaatgtgccgcaa[A/G]tataaaatagacaca | 9169 |
rs12314576 | snp | C/T | 0.19459 | 0.243782 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939466 | tttgggaggccgaga[C/T]gggcagatcatctga | 9169 |
rs12810922 | snp | C/G | 0 | 0 | missense | SCAF11 | GRCh38.p7 | 12:45928363 | ATTGCAACTTTTCAA[C/G]CAATTAGCAGACTGG | 9169 |
rs12813075 | snp | A/G | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928362 | CATTGCAACTTTTCA[A/G]GCAATTAGCAGACTG | 9169 |
rs12813334 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972909 | atatatatatatata[G/T]atatatatatagata | 9169 |
rs12813583 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972911 | atatatatatataga[G/T]atatatatagatata | 9169 |
rs12813613 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972949 | atatagatatatata[G/T]agatatatagatata | 9169 |
rs12813623 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972961 | atatagatatataga[G/T]atatatatagatata | 9169 |
rs12813624 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972969 | atatagatatatata[G/T]agatatatagatata | 9169 |
rs12813634 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972981 | atatagatatataga[G/T]atatagatatagata | 9169 |
rs12813648 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973003 | atatagatatataga[G/T]atatatatagatata | 9169 |
rs12813804 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973011 | atatagatatatata[G/T]agatatatagatata | 9169 |
rs12813811 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973023 | atatagatatataga[G/T]atatagatatagata | 9169 |
rs12814578 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954226 | TTTTCCTTTACAAtt[G/T]tttctttattttttt | 9169 |
rs12814816 | snp | A/C | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937705 | actttggaaaattat[A/C]ataatcaagactgcc | 9169 |
rs12828693 | snp | C/T | 0.310337 | 0.24261 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992065 | CTGCATTCTCGCAGA[C/T]TACGTTGCGGCGTCC | 9169 |
rs12830075 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972951 | atagatatatatata[G/T]atatatagatatata | 9169 |
rs12830080 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972959 | atatatagatatata[G/T]atatatatatagata | 9169 |
rs12830094 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972971 | atagatatatatata[G/T]atatatagatatata | 9169 |
rs12830097 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972979 | atatatagatatata[G/T]atatatagatataga | 9169 |
rs12830107 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972987 | atatatagatatata[G/T]atatagatatataga | 9169 |
rs12830287 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973013 | atagatatatatata[G/T]atatatagatatata | 9169 |
rs12830293 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973021 | atatatagatatata[G/T]atatatagatataga | 9169 |
rs12830297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973029 | atatatagatatata[G/T]atatagatatataga | 9169 |
rs12830942 | snp | A/G | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954206 | GACATCAGCTAAATT[A/G]CATTTTTTCCTTTAC | 9169 |
rs12831208 | snp | C/T | 1.64999e-05 | 0.00287222 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922914 | ACAGAATTATGAAGG[C/T]TGCTCTCAACCTTGA | 9169 |
rs13377610 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949301 | taaattggaatgtgc[C/T]gcaagtataaaatag | 9169 |
rs17096327 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938714 | AACATCCTTTTGTAC[A/G]ATACAAACAAGTATA | 9169 |
rs17096331 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939374 | GTTTAAAGAACAGTC[C/T]CATCCTGCTTCACAA | 9169 |
rs17096332 | snp | A/C | 0.0463947 | 0.145069 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940599 | AAATGATGTTAATAC[A/C]TAATCTCAGAAGACA | 9169 |
rs17096346 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944591 | CCTCGCTTACAAACA[A/G]ATCATAGTAAGATGT | 9169 |
rs17096347 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947445 | CATAAACACTTGTTA[C/T]AGTAGACAGCAAGTG | 9169 |
rs17096358 | snp | C/G | 0.0463947 | 0.145069 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955005 | GAAAAGGCTCCACTG[C/G]TATTACAAAAACACA | 9169 |
rs17096361 | snp | C/T | 0.417845 | 0.185278 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955076 | TACTGCCATATATCA[C/T]CACAATCTATATAAA | 9169 |
rs17096380 | snp | A/C | 0.390838 | 0.206555 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967889 | CTATCTGCCTGGACT[A/C]CAGTTTTCAATCCAA | 9169 |
rs17719679 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940731 | TAAAACAGTTTCACC[A/G]CATTGTATCTCAATG | 9169 |
rs17837442 | in-del | -/T | 0.197393 | 0.244402 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934896 | TACCTGTTTTCTAGA[-/T]GATAGCTGGAAAAGA | 9169 |
rs28364643 | snp | A/T | 0.00416161 | 0.0454256 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928462 | AGAAACAGCAGAATC[A/T]GACACATCACCTGTG | 9169 |
rs28734893 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924035 | TTTGTATTTTTAGTA[A/G]AGGCAGGGTTTCACC | 9169 |
rs28762132 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972879 | CGATATATATATATA[G/T]AGATATATATATAGA | 9169 |
rs28773238 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972887 | ATATATATAGATATA[G/T]ATATAGATATATATA | 9169 |
rs28805360 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972939 | ATATAGATATATATA[G/T]ATATATATATAGATA | 9169 |
rs28837853 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972897 | ATATATATATAGATA[G/T]ATATATATATAGATA | 9169 |
rs28846111 | snp | G/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972937 | ATATATAGATATATA[G/T]AGATATATATATAGA | 9169 |
rs28856410 | snp | G/T | 0.472241 | 0.114494 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972945 | ATATATATAGATATA[G/T]ATATAGATATATAGA | 9169 |
rs28888779 | snp | G/T | 0.0368353 | 0.130617 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972917 | ATATATAGATATATA[G/T]ATAGATATATAGATA | 9169 |
rs28896898 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972908 | GATATATATATATAT[A/C]GATATATATATAGAT | 9169 |
rs28930670 | snp | C/T | 0.0480599 | 0.147378 | missense | SCAF11 | GRCh38.p7 | 12:45927161 | TTTGGGGACTGAGAA[C/T]GGGATTTTTTCCGGC | 9169 |
rs34091380 | in-del | -/T | 0.469445 | 0.119766 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954939 | CCCCCCCTTTTTTTT[-/T]CCTTAAGCATAATTG | 9169 |
rs34185623 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941823 | ATGTGTTTGAACTCC[-/C]ATGGGTCTGCTTATT | 9169 |
rs34195479 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940302 | GCTATCAAAATGAAA[-/A]GAGAACTAATTTTAC | 9169 |
rs34242259 | multinucleotide-polymorphism | CT/TC | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990247 | AAACTTTGTCAGCCC[CT/TC]GCGTCGCCCTAGGCC | 9169 |
rs34300243 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977823 | CAGCACTGACAGTTC[-/C]TGAGAGACAACAGAT | 9169 |
rs34305226 | snp | A/C | 0 | 0 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991794 | CTCAGTGTCCCCCAT[A/C]TACCAGCTGACCTTC | 9169 |
rs34308236 | in-del | -/C | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45960960 | ATGAACAATAATTTT[-/C]TTACTTAACATTTCA | 9169 |
rs34342321 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984776 | TTGGCCCACTGCAAA[-/A]CTCCACCTCCCAGGT | 9169 |
rs34474948 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965242 | TTACAATGGAAGGAG[-/T]ATTATAAGCAGAGAT | 9169 |
rs34591032 | in-del | -/T | 0.194278 | 0.243711 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944787 | ATATGTTAGAGGTGC[-/T]TTTATTTCTAAAGTT | 9169 |
rs34665170 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953255 | GTTCATATATTTTTT[-/T]AATAATGCATTGTCT | 9169 |
rs34705963 | in-del | -/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919775 | GAAATAATTCATGGG[-/G]AGTGCTACTAAAGAT | 9169 |
rs34799538 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991957 | TTCTGTTCGCGCGTG[A/C]TGCGCTCTCCAGCCA | 9169 |
rs34861484 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981325 | GAATGAACTCATCCC[-/C]TAAAACAAACTATTC | 9169 |
rs34887909 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940307 | CAAAATGAAAGAGAA[-/A]CTAATTTTACATTAA | 9169 |
rs34900990 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955194 | AAACAGGGTCTCACC[C/T]TCTTGCCCAGGCTGT | 9169 |
rs34994858 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957269 | AATTCCAGATAATAA[-/G]AGCTTTACTGAATTA | 9169 |
rs35174436 | in-del | -/TT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930470 | TGTTTTTTTTTTTTT[-/TT]GAGACAGGCTGTTGT | 9169 |
rs35192493 | in-del | -/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919737 | CCAAATCAGACATGG[-/G]AACACACACTTGTTA | 9169 |
rs35196486 | snp | C/T | 0.444444 | 0.157135 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932467 | ACATCTGGAATTCTT[C/T]ATCTGACTTCTATTA | 9169 |
rs35347796 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954569 | TAATCTAAGCTGTTA[-/C]TTTTTTTTTTTTTTT | 9169 |
rs35402877 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981146 | TAATCTTATTATAAA[-/A]TGCTACAAACTGCCA | 9169 |
rs35425343 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989986 | CCCTTCCCCCCCCCC[-/C]GTAGGACCCTGCACC | 9169 |
rs35487712 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979939 | TGAATAGATATTGGG[-/G]ATTCTTTCCTAAATG | 9169 |
rs35506348 | in-del | -/C | | | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45927142 | TCTCTTGCAATATCC[-/C]TTTTTTGGGGACTGA | 9169 |
rs35513335 | in-del | -/C | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993036 | TATGCAGCATCCTCC[-/C]TTATTATGTTTGGAT | 9169 |
rs35536609 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941894 | CTCTCCTGCCTCCCC[-/C]TTCCACCTTTTCTGC | 9169 |
rs35623702 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934523 | TACAAAGACATAAAA[-/A]GGACTTGGTTACCTT | 9169 |
rs35675242 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977873 | CAGAGATTAAAAACA[-/C]ACAGGCTCAATTTAA | 9169 |
rs35684255 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940967 | TATCACCACACTTGG[-/G]CTAATTTTTGTATTT | 9169 |
rs35779048 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939050 | TTTGCTAATAGGTTT[-/T]GCTGTCTAACCTTTC | 9169 |
rs35900560 | in-del | -/C | | | frameshift-variant, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961843 | GGAAATAGTATTATC[-/C]TCCGTTTTCTTCACC | 9169 |
rs35965551 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968176 | CTGTAAGTTAATTAT[-/A]CTATAAGTCAAATTG | 9169 |
rs36058160 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945556 | TGTATTATCTCAGTC[-/T]TTTTTTTTTTTTTTT | 9169 |
rs36060348 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954587 | TTTTTTTTTTTTTTT[-/T]AACACAGGGTTTCAC | 9169 |
rs36119551 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943283 | GGTCAAATGCAGCCC[-/C]AAAAATATTAAGTGG | 9169 |
rs55655357 | in-del | -/CACA/CACACACA/CACACACACA | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983785 | ACACACACACACACA[-/CACA/CACACACA/CACACACACA]AAGACTGAACTAATT | 9169 |
rs55966315 | in-del | -/A | 0.425277 | 0.178263 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946642 | GTAATTTTGAGGGAG[-/A]AAAAAAAAAATGCAT | 9169 |
rs56146240 | snp | C/T | 0.375598 | 0.21616 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938345 | AATACCAAAATTAGC[C/T]GGGCATGATGGCGGG | 9169 |
rs56361433 | in-del | -/AA | 0.417359 | 0.185718 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938502 | CTCAAAAAAACAAAC[-/AA]ACAAACAAACAAAAA | 9169 |
rs57470002 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933826 | AGTCACTAGGATTCA[A/G]AGATGAATGGATCAG | 9169 |
rs57613185 | snp | A/G | 0.0463947 | 0.145069 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982908 | CTGTATCACTTCCCG[A/G]TACAAGGAGTAGACT | 9169 |
rs58184670 | in-del | -/T | 0.195526 | 0.243993 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932359 | TGATTCAATATAAGG[-/T]TAAGATTCTGGAGTA | 9169 |
rs59166912 | in-del | -/ACAA/ACACAA/CA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983784 | CACACACACACACAC[-/ACAA/ACACAA/CA]AAAGACTGAACTAAT | 9169 |
rs59662890 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965442 | AAGGATGTTAATATG[G/T]CAAAGGCAAGAAATT | 9169 |
rs59757955 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940305 | TATCAAAATGAAAGA[A/G/T]AACTAATTTTACATT | 9169 |
rs60140747 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929109 | AGAGAAAAAAAAAAA[-/A]GGAAAATAACTTTTG | 9169 |
rs60309540 | in-del | -/C | 0.195214 | 0.243923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936976 | TGTAACCCCAATCCT[-/C]TATGTGGTCTGTTTT | 9169 |
rs61009645 | snp | A/G | 0.195837 | 0.244062 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948060 | AATAAACTGAAAAGA[A/G]CGAATTCTTTTAATT | 9169 |
rs61924069 | snp | A/C | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938503 | TCAAAAAAACAAACA[A/C]ACAAACAAACAAAAA | 9169 |
rs61924070 | snp | A/C | 0.417359 | 0.185718 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941626 | TCTTCATTATACCCT[A/C]CCAAACGTTCTCCCA | 9169 |
rs61924071 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966987 | TCAGATGTAATATAT[C/T]ATCCCTTTATGTAAC | 9169 |
rs61924072 | snp | A/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974395 | CTTTCACAAAAAATT[A/T]CTCTGTGTACAAGAT | 9169 |
rs61925818 | snp | A/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928869 | AAGTACCTAATAATA[A/T]TTAAAAAAAAAAAAA | 9169 |
rs61925819 | snp | G/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929164 | TTTTTTTTTTTTTTG[G/T]AGACAGGGTCTCACT | 9169 |
rs61925820 | snp | C/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931020 | CGTTTCACAATTGAT[C/T]TTTAGAACTTATTCT | 9169 |
rs66481242 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979204 | CCATCCATGAGGGCA[G/T]AGCCCTCACAGCCTA | 9169 |
rs67136007 | snp | G/T | 0.417845 | 0.185278 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987800 | CATGACCTGACATTT[G/T]ATCAGGATCACTCTG | 9169 |
rs67656438 | in-del | -/GA | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972900 | ATATATAGATATATA[-/GA]TATATATAGATATAG | 9169 |
rs71437738 | in-del | -/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945537 | TGTATTATCTCAGTC[-/T]TTTTTTTTTTTTTTT | 9169 |
rs71437739 | in-del | -/ACAC/ACACAC/ACACACAC | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983742 | ACTCCTAAACCTAAA[-/ACAC/ACACAC/ACACACAC]ACACACACACACACA | 9169 |
rs71437740 | in-del | -/C | 0.5 | 0 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45990612 | CCTCCTCCCTCCCCT[-/C]CCCTCCCTGCGCGTC | 9169 |
rs71437741 | in-del | -/C | 0.5 | 0 | utr-variant-5-prime, intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45990616 | TCCCTCCCCTCCCCT[-/C]CCCTGCGCGTCTCCC | 9169 |
rs71445722 | snp | A/C | 0.444444 | 0.157135 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972920 | TATAGATATATATAT[A/C]GATATATAGATATAT | 9169 |
rs71461193 | snp | A/C | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981019 | GTGATTTATAAATTA[A/C]CAAAATAAAGAAATA | 9169 |
rs71461194 | snp | A/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987921 | ACGTTATGTATTGAA[A/T]TTTTATGTGTCTATG | 9169 |
rs71461195 | snp | A/G | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988167 | TTATTTCACTGGGCA[A/G]GGTAAGTCAAGGTAC | 9169 |
rs71724498 | in-del | -/GT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964929 | AAACAGTGGGTGAAA[-/GT]GTGTGTGTGTGTGTG | 9169 |
rs72022912 | in-del | -/GTTTCACAAATC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935892 | GGTTTCCTGAAGATC[-/GTTTCACAAATC]CACCCTACTTGTCTG | 9169 |
rs73097372 | snp | C/T | 0.000737191 | 0.0191847 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953789 | AGTCTCTCTGTGCCT[C/T]AGTAACCTTATTTGT | 9169 |
rs73097380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984503 | TAATATCATCCAAGC[A/G]TCTTCACTGTAAAGT | 9169 |
rs73292563 | snp | C/T | 0.00402967 | 0.0447057 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927919 | TGTAAAATCTTTATG[C/T]TCAGTAATTTCTACT | 9169 |
rs73292567 | snp | A/T | 0.0166325 | 0.0896639 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935205 | ACTAACTAGGAGGCT[A/T]GTTTCCTGCACTGCA | 9169 |
rs73292573 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943900 | ATCCAATCTAATATG[A/C]CACATTCTAAACAGT | 9169 |
rs73292583 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969278 | CAGGGTTCCTAATAA[C/T]GTAAACTATTCTTTA | 9169 |
rs74081611 | snp | C/G/T | 0.0595055 | 0.16192 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974170 | TGTCTAAAAACTGTA[C/G/T]ATACTTGATTTAAAA | 9169 |
rs74318498 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981009 | AACAGGGCAGGTGAT[C/T]TATAAATTAACAAAA | 9169 |
rs74529533 | snp | G/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930470 | TGTTTTTTTTTTTTT[G/T]TGAGACAGGCTGTTG | 9169 |
rs74564685 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984019 | CTTTTACAAAAAGGA[A/G]TAAGTATAAACTTTA | 9169 |
rs74660698 | snp | A/G | 0.0435539 | 0.140996 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926638 | TTCTGTTATCCAATT[A/G]GGACAGTCATTTCTA | 9169 |
rs74695797 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944636 | TAAACAGCCTGAACC[C/T]CCAAGGAGGAGTCAC | 9169 |
rs74697654 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939659 | GCCGAGATCGTGCCA[C/T]TGAGATCGTGCCATT | 9169 |
rs74713007 | snp | G/T | 0.00167882 | 0.0289239 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45923032 | GGCTTTGCTGTGACT[G/T]GATGACGAAGTATTA | 9169 |
rs74729181 | in-del | -/TT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939743 | AAATAAGAAAACAAG[-/TT]AAGCTAAGCTAAGTA | 9169 |
rs74770310 | snp | G/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954052 | AATCCAAGTACTTCA[G/T]TATTTTAGCTATTTT | 9169 |
rs74807919 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952303 | ATATGTGTATCTTTT[C/T]AATATATAAACTTAA | 9169 |
rs74916380 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988027 | AAGAGAATGATACTG[A/G]ATATTTTAACTCTGG | 9169 |
rs75023600 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965340 | ATTCTGAGATTTGGT[A/G]AGCAACTACAGTGAA | 9169 |
rs75091769 | snp | A/G | 0.0471551 | 0.14613 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966634 | TCAGAAAGCAGCAAG[A/G]GAGACAGTTATGTGA | 9169 |
rs75369964 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935466 | ATACGCTGATTTTTT[A/C]AAATGGCTTAAGAGG | 9169 |
rs75373887 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45960941 | CTTAGAAAATATAGC[A/G]TAATATGAACAATAA | 9169 |
rs75429048 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973721 | TAAAATGGAAAAGAA[C/G]TGTAAACCTAAAATC | 9169 |
rs75454888 | snp | A/C | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955181 | TAATTTTTTTTTTAA[A/C]CAGGGTCTCACCCTC | 9169 |
rs75460970 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966388 | CTATAGGTATACTAG[C/G]CAATTCTCTTAGTAC | 9169 |
rs75478291 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964910 | CAATTGAGCGGGTGA[A/G]AGAAAACAGTGGGTG | 9169 |
rs75526996 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943314 | AAAATTCCAGATACA[A/G]ACAATTCTTAAGTTT | 9169 |
rs75627410 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963438 | AAAAAAAATGAGTAA[C/T]ATCTTCAAAGTGCTA | 9169 |
rs75629819 | snp | A/T | 0.00597247 | 0.0543191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940739 | TTTCACCGCATTGTA[A/T]CTCAATGAAAAAAAC | 9169 |
rs75704343 | snp | C/T | 0.0667028 | 0.170006 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933057 | TTGAATAAGGTACCC[C/T]TGTACTTAAGTACTA | 9169 |
rs75742176 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941252 | AGACACCTTACTTAT[C/T]GAAAAACGAATTTGC | 9169 |
rs76129944 | snp | A/G | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965610 | TAAGCCACTGCACCT[A/G]GCCTTAAATCAACTC | 9169 |
rs76135349 | snp | C/G | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937213 | TCTTAAATGAATATC[C/G]TATCATCTCTTTTTT | 9169 |
rs76158253 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947984 | ACCTGGCCAGCATTC[A/C]GAAATTTTACATTGC | 9169 |
rs76367617 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978050 | AGAATATATTTACAA[C/T]GCAGTACTTTATTTA | 9169 |
rs76388600 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952207 | TGAAGTACTCCTTCA[C/T]CCCTCCCCTCAGCCA | 9169 |
rs76460162 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970389 | GTTACACAGAAAGAA[A/G]AGGGATATAAATGGC | 9169 |
rs76502240 | snp | A/C | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937030 | GACTTCTAGAACTTT[A/C]TGAAGTATTTGGTAT | 9169 |
rs76567063 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930554 | AACCTCCCAGACATT[C/T]ACAACACTTGAGTAC | 9169 |
rs76701678 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965695 | ATGCATTTATATCTA[C/T]GCACAAGAAATCCTT | 9169 |
rs76785973 | in-del | -/AAAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972604 | AAAAAAAAAAAAAAA[-/AAAA]TCCAAAAAACAAAAA | 9169 |
rs76795824 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986832 | CTCATTTTCTCTTGC[A/C]ACCAACCACTATGTA | 9169 |
rs76820670 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974087 | TAAAGCAAGTCACAC[A/G]AAATTTTTGGTTTCC | 9169 |
rs76825371 | snp | C/G | 0.0162398 | 0.0886349 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981877 | AAATAATCGTGCACA[C/G]CAATTAAAAGAGATT | 9169 |
rs76913994 | snp | A/G | 0.0115144 | 0.0749975 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920895 | AACAGCCTAACAGCA[A/G]TTCTCGAATTGGCAC | 9169 |
rs76947267 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987955 | TAGGATTTCATACAT[A/T]AAGTTCATAGACACA | 9169 |
rs77018252 | snp | G/T | 0.0105312 | 0.0717963 | missense | SCAF11 | GRCh38.p7 | 12:45928710 | GAGACTGACTGGCTG[G/T]TTCAGCTCTTGTGTT | 9169 |
rs77027073 | in-del | -/AA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964665 | AGTGAGACTCTGTCT[-/AA]CAAAAAAAAAAAACG | 9169 |
rs77037623 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931673 | TAAACCACCAATTTA[A/G]AAGTATTAATTCTCT | 9169 |
rs77065356 | snp | A/G | 0.0256215 | 0.110247 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974600 | ACAACTCTTCATTCA[A/G]AATTTATCATAAAAT | 9169 |
rs77098117 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949641 | GGGAGAGAAAACTGG[A/C]AAAGTCCCAGATATT | 9169 |
rs77118508 | in-del | -/TAAAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45928871 | GTACCTAATAATATT[-/TAAAA]AAAAAAAAAAAGTAA | 9169 |
rs77384084 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979109 | GATTAGGCTGTGAGG[-/G]CTATGCCCTCATGGA | 9169 |
rs77406962 | snp | C/T | 0.046775 | 0.145601 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976490 | CATAGAGTTTGGTAC[C/T]ATCTGTAGTTTCAGG | 9169 |
rs77492031 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954024 | AATTTGCAAAGTTTA[A/T]GACGTAGATGGAAAT | 9169 |
rs77797790 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985637 | ACATTGCAAGGCTAC[C/T]GAAAAGATCAAATGA | 9169 |
rs77854435 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950199 | TGTAAAATAAGATAA[C/T]AGAGGTAAATGTTCT | 9169 |
rs77951454 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980046 | CTTTCTAACAGGTCA[C/T]GAATGATCTCATTTA | 9169 |
rs78077540 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45974082 | TGCAATAAAGCAAGT[C/T]ACACAAAATTTTTGG | 9169 |
rs78102705 | snp | A/G/T | 0.0463947 | 0.145069 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954426 | ATTTTTCATAGAGAT[A/G/T]GGGTTTTACCATGTT | 9169 |
rs78108275 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952720 | TTAAGATGAAATGTA[C/T]TTTCTATTAGGGTAG | 9169 |
rs78133828 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954737 | ACCGTGCCTAGCTTT[C/T]TTTTTTTTTTTTTTT | 9169 |
rs78207461 | snp | G/T | 0.0260105 | 0.111035 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933958 | CAAAGCACACTGGCA[G/T]AGGCAATCACTGCAC | 9169 |
rs78228040 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933667 | AGCCTACTTAGACAT[A/C]ATTTTTTTCTTGGTA | 9169 |
rs78373000 | snp | C/G | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936765 | ATTTTCTGAATCTCA[C/G]ATTGTTCTTCCATTT | 9169 |
rs78420182 | snp | G/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930456 | TTTTGTTTTTTTTTT[G/T]TTTTTTTTTTTTTTT | 9169 |
rs78427791 | snp | C/T | 5.71004e-05 | 0.00534294 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964088 | TCAACAAACAAACTT[C/T]ATAAAAATGAAAAGT | 9169 |
rs78586984 | snp | A/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955178 | TCATAATTTTTTTTT[A/T]AAACAGGGTCTCACC | 9169 |
rs78673141 | snp | A/G | 0.0460142 | 0.144533 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931826 | AACCTTTAAAAGTAT[A/G]TTTTTCTGATAAATT | 9169 |
rs78688470 | snp | A/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959272 | GACTCTGTCTCAAAT[A/T]AAAAAAAAAAAAGAA | 9169 |
rs78731024 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969474 | TGGTATCTAAAGATA[C/T]CTACATCCTGGTTAA | 9169 |
rs78773602 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985519 | AGGCCGAAAGTCAGA[C/T]GGACCCAGCTATAGA | 9169 |
rs78883317 | snp | A/G | 0.0154538 | 0.0865337 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993468 | TCATGCTGTAAATAT[A/G]CTGGATTGAAAAACA | 9169 |
rs78984577 | snp | C/T | 0.0275645 | 0.114116 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920705 | ACAGGTTTTACTGTC[C/T]AGAATTTTGCAACAT | 9169 |
rs78987594 | snp | C/T | 0.0147659 | 0.0846458 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45948508 | ATTTTTCTTGTCTTT[C/T]GTTTCTCTCAGCTGT | 9169 |
rs79029317 | snp | C/T | 0.0850919 | 0.187897 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978634 | AGAAGAAAGGCATCT[C/T]GGATGGACGTATGGA | 9169 |
rs79060756 | snp | G/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935703 | CTCAGAAAGCCATCA[G/T]TAGATAAAATGCTCT | 9169 |
rs79114664 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954939 | AGTAAGATTCCCCCC[C/T]TTTTTTTTCCTTAAG | 9169 |
rs79118680 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983256 | GAGAGATGGAAAGTA[C/T]GAGAAACTAGTTAGG | 9169 |
rs79208857 | snp | A/T | 0.00517822 | 0.0506191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951935 | AATGATGAACGAGAC[A/T]GAATCTGTTATTAAA | 9169 |
rs79241379 | snp | A/C | 0.0193772 | 0.0965046 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939378 | AAAGAACAGTCCCAT[A/C]CTGCTTCACAAAACT | 9169 |
rs79263241 | snp | A/T | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966340 | GATCTTTTGTGGGAT[A/T]TTTTTTTTTTTAGCT | 9169 |
rs79502832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942008 | GATCCACTTCTGCTC[A/T]ATGAACAGTAAATGT | 9169 |
rs79683148 | snp | G/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929162 | AATTTTTTTTTTTTT[G/T]GGAGACAGGGTCTCA | 9169 |
rs79688489 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944910 | TTACAGTAACTGGCC[C/T]ACAAGGTATTTAATC | 9169 |
rs79901901 | snp | C/G | 0.00993419 | 0.0697739 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919404 | AATGTTAATGGATAA[C/G]TACTATTAGTCTCAA | 9169 |
rs79922365 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989839 | AAAGTTTGGTTTCAC[C/T]AGCGGGCTTGGACGC | 9169 |
rs79987767 | snp | C/T | 0.107694 | 0.205546 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937704 | TACTTTGGAAAATTA[C/T]AATAATCAAGACTGC | 9169 |
rs80019043 | snp | G/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921543 | CTTTAAAAATACACA[G/T]TAGGAACTTTGCAAC | 9169 |
rs80100201 | in-del | -/CTT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954733 | TATCACCGTGCCTAG[-/CTT]TTTTTTTTTTTTTTT | 9169 |
rs80339178 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956329 | TAGAGCATGTTATAC[A/G]AAATTCTAGTTCAAA | 9169 |
rs111280279 | snp | A/G | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947703 | TGTTTTTGAGACAGA[A/G]TCTTGCTCTGTTGCT | 9169 |
rs111440168 | snp | A/G | 0.5 | 0 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920606 | TCTAGTATTAAAAAG[A/G]GAAAAAAAAAAAAAC | 9169 |
rs111522666 | in-del | -/AAAC | 0.0150606 | 0.0854603 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938493 | GACTGCATCTCAAAA[-/AAAC]AAACAAACAAACAAA | 9169 |
rs112366533 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | SCAF11 | GRCh38.p7 | 12:45928727 | TCAGCTCTTGTGTTA[C/T]GTGTAGACCTCCTTG | 9169 |
rs112408747 | snp | A/C | 0.5 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922885 | AAGCTGATATTTTTT[A/C]TCCTTTATCATATAC | 9169 |
rs112445405 | in-del | -/G | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979107 | GTGATTAGGCTGTGA[-/G]GGCTATGCCCTCATG | 9169 |
rs112659872 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936433 | AGGCATGAGCCACCA[C/T]GCCCAGCCAGCTTCA | 9169 |
rs112858085 | snp | A/G/T | 3.295e-05 | 0.00405881 | synonymous-codon, missense | SCAF11 | GRCh38.p7 | 12:45926808 | ATCTTCCCTTCCACC[A/G/T]GGGAGAGTAACTATC | 9169 |
rs112867715 | in-del | -/GCTT | 0.5 | 0 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918993 | TATAGCTAACTCTAA[-/GCTT]GCTTTAGAGCTTGGG | 9169 |
rs112966624 | snp | A/C/G | 0.0186075 | 0.0947518 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954937 | TGAGTAAGATTCCCC[A/C/G]CCTTTTTTTTCCTTA | 9169 |
rs112985183 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924558 | TCTAATTTGGGAGTT[A/G]GGGGGTTTTGAGAAG | 9169 |
rs113074395 | snp | C/T | 0.0248432 | 0.108648 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948243 | CAGCCAGAACCAATT[C/T]TTCACCAAAAACAGA | 9169 |
rs113296831 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972996 | TATATAGATATAGAT[A/C]TATAGATATATATAT | 9169 |
rs113492271 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973645 | ATGATTTGAATCACC[A/G]GTGATTTCTTATCAG | 9169 |
rs113580226 | snp | G/T | 0.5 | 0 | missense | SCAF11 | GRCh38.p7 | 12:45924834 | ACACTGGTAGGAGTG[G/T]CTACCTGCATGAGGG | 9169 |
rs113944543 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934662 | CAATTTTCCCAAATG[C/G]TGATTTCATCTTACC | 9169 |
rs113999748 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946880 | TAGGCTCTTGGAGGG[A/G]GTATTCCATGAATAC | 9169 |
rs114146473 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971457 | GTAAATAATAGCATA[C/T]GGACTAGAGAAGACA | 9169 |
rs114180943 | snp | G/T | 0.00313603 | 0.0394738 | missense | SCAF11 | GRCh38.p7 | 12:45926528 | AAGTTTTTATTCCAA[G/T]AATTTCCTGAATTTT | 9169 |
rs114233687 | snp | A/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45994010 | ACTAAAAATAAAATT[A/T]AAAAAATGACCAGCT | 9169 |
rs114248768 | snp | G/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947809 | AACTTCCTAAGTAGC[G/T]GGAACTGCAGCCATG | 9169 |
rs114261962 | snp | C/G | 0.0460142 | 0.144533 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993392 | CTTTTTCAGAAATAA[C/G]TGCTATTTTAATTTA | 9169 |
rs114263651 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937730 | ACTGCCAGTGCTTTG[A/G]AAAATGCTCTTAGGT | 9169 |
rs114269562 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990037 | CAGCTAAGGCGGCGG[A/G]AGACGCGTAGGCCAC | 9169 |
rs114412547 | snp | C/G/T | 0.013105 | 0.08 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948771 | ATTAAGTGCTTATAA[C/G/T]AGAGATATGAACACA | 9169 |
rs114415796 | snp | A/C | 0.0134861 | 0.0810011 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982067 | TAAACCTTTTTAAAG[A/C]GTCTAAGTGGATTTG | 9169 |
rs114476976 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951146 | CAGAATTTAATTTTA[C/T]TGGCTAATTTCAAAA | 9169 |
rs114506482 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945929 | ACCCCGGATCTCAAG[C/T]GATTCTCCCCCTCAG | 9169 |
rs114511815 | snp | A/G | 0.0107246 | 0.0724382 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920729 | GCAACATGGCTAATG[A/G]CTACCACCTGGTCAC | 9169 |
rs114514254 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943137 | AAGAAAAACTGACCA[C/T]GTTAGACTTATCAAA | 9169 |
rs114544463 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950687 | TACAACAAGCAAACC[A/G]TTTATTTGAATTGCA | 9169 |
rs114609433 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989469 | TATGTAATACAATAC[A/G]GAAATATATTGGAAG | 9169 |
rs114628877 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981005 | GGGAAACAGGGCAGG[A/T]GATTTATAAATTAAC | 9169 |
rs114631126 | snp | C/T | 0.0168055 | 0.0901129 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932737 | AGGCACTTGATCAAA[C/T]AGTTATTTAGAAAAA | 9169 |
rs114685849 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971647 | TGGGTAAGGGGGAGG[A/G]GAGCTGGGGGTAAGG | 9169 |
rs114755505 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986337 | GTAATCCAGAAATCA[C/T]CTTTCAAATTTCTTT | 9169 |
rs114760412 | snp | C/G | 0.00716266 | 0.059414 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992258 | CTGTCAAAGTCTTTG[C/G]AGTTTTTCAGTGTAC | 9169 |
rs114785576 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966305 | ATCTATCAATGAAAG[C/T]ATTCAAGCAAAGGCC | 9169 |
rs114822904 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956807 | ATATTCTGACATTTA[A/C]AACTAGGCACAAAGA | 9169 |
rs114823065 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974929 | AATAAGACTTAACAG[C/T]CAAAATTACTTCTTG | 9169 |
rs114845390 | snp | C/T | 0.00146139 | 0.0269919 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991948 | CTGCCCCCGTTCTGT[C/T]CGCGCGTGCTGCGCT | 9169 |
rs115011438 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969885 | AGGACTGCAGGTGCA[C/T]ACCACCACATTCAAC | 9169 |
rs115020580 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940014 | CTGTCTTTTCTGTTG[C/T]GTGACAGACTCATTT | 9169 |
rs115021305 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954304 | TGGCACTATCATGGG[C/T]CACTAAGGCCTTTGC | 9169 |
rs115022741 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989138 | TGTCAAAATTTTAAT[A/G]CAATTACTAATAAAA | 9169 |
rs115184073 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978150 | GACAGGCTTCCATTA[C/T]TTCTCCAAATAAGAA | 9169 |
rs115199683 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950710 | GAATTGCAGTCCTGT[A/T]TGTACCTTGCATCAA | 9169 |
rs115285909 | snp | C/G/T | 0.0217236 | 0.101931 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934606 | GCAAGGGTTGAAATA[C/G/T]GTAGAAAAGCTGTAT | 9169 |
rs115343245 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971775 | ATCTGGTGATGGTAG[C/T]GGGTGCAACAGTGGC | 9169 |
rs115568419 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944330 | TTTGCTTCAATTTCA[C/T]TTTAATAGTAAAATT | 9169 |
rs115571922 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957168 | GTACATTTACATTAC[C/T]GTTCACAGAGAGCTA | 9169 |
rs115573477 | snp | G/T | 0.00138677 | 0.0262957 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974226 | AATCATCTCAGCAAG[G/T]CTTCAGCAAGTCATA | 9169 |
rs115622524 | snp | A/C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951390 | CAAAACGTCCTTCAG[A/C/T]TTATCAGAGATCTAA | 9169 |
rs115790404 | snp | G/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954712 | AGTAGCTGGGATACA[G/T]GCATGTATCACCGTG | 9169 |
rs115819509 | snp | C/T | 0.024105 | 0.107105 | missense | SCAF11 | GRCh38.p7 | 12:45927949 | TAGGGAACTCTCTGT[C/T]ATTTTTTCTTCATTA | 9169 |
rs115895989 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989984 | GCCCCTTCCCCCCCC[A/C]CCGTAGGACCCTGCA | 9169 |
rs115926480 | snp | C/T | 0.0422008 | 0.138995 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972788 | ACACCACCAAGATGA[C/T]ACAGCTGGGTGAATT | 9169 |
rs115936842 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953641 | CTATTTTAAAGGTAA[A/G]TTTAGAGAAACATTA | 9169 |
rs115937275 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963150 | AATGAGGTTACAGAA[C/T]GGTCTAACATACTAA | 9169 |
rs116103118 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976029 | GATGCAGAATTGCCA[C/G]AATCTTCAATTTGTA | 9169 |
rs116171367 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987990 | AAAAAAATACAATGC[A/G]AAGATGAGTTTTGGG | 9169 |
rs116272846 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983147 | TGGACTTCAAGTCTA[C/T]CTCTCTCCCATTTAT | 9169 |
rs116355788 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987907 | GTGGTTGTGTTTTTA[C/T]GTTATGTATTGAATT | 9169 |
rs116410858 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972081 | GTGGATTTAAACCCA[A/G]GCAGCATACCACCGA | 9169 |
rs116414996 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45962926 | AAACCTAAGAAAATA[A/T]GCTGTCTTGAGTGAG | 9169 |
rs116586892 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975454 | GGTCTTCTGGATAAC[C/G]TGATGCAGCTTCCGC | 9169 |
rs116657830 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936102 | TTCTAACATTTACTT[A/G]TTACTAAATAACACC | 9169 |
rs116670604 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989456 | CTGGTAGACACTGTA[C/T]GTAATACAATACGGA | 9169 |
rs116686369 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962015 | CTGCTTGAGCCCAAC[A/G]TGCCCAACATTTACT | 9169 |
rs116740807 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941570 | TCTCCCTATCTTCCC[C/T]GCTCCCAAAAACCAC | 9169 |
rs116813767 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965081 | CAATGTAAATCAAGT[A/T]TGGCTAGATTATAGA | 9169 |
rs116828610 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945400 | TTCTCCTCCATCAAA[A/G]TGAAATCTATCATGC | 9169 |
rs116994572 | snp | A/G | 0.029116 | 0.117091 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989699 | GTAGTTGTCAGCCCA[A/G]GTAGCGAATTTAAAA | 9169 |
rs117034579 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954614 | TCACTCTGTCGCCCA[C/T]GCTGGAGTGCAGTCA | 9169 |
rs117383400 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933306 | ATTAGGTTGTACAAA[C/G]AATAGCAGTCGTTTT | 9169 |
rs117421238 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941612 | TTCCAAAAGAGAATT[A/C]TTCATTATACCCTCC | 9169 |
rs117456353 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919643 | TAAAGCATGCATTTT[C/T]TAATACATTCTTAAA | 9169 |
rs117462487 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981924 | AAGAAAGACTGAATT[A/G]TATGCCTGTCTACAA | 9169 |
rs117473958 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963190 | AAAAGAGAATAAAGG[A/G]AAGGCAACAAAGAGG | 9169 |
rs117507015 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967348 | ACTGCCTTTGTTAGA[A/T]ATCTGCCTTAATGGC | 9169 |
rs117605270 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925171 | TAAAATTAAATAGCA[A/G]TTAATAGGCTCAGTA | 9169 |
rs117614828 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980686 | TATTTATGTAACTAA[C/T]TAAGTAACATTTATC | 9169 |
rs117675993 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939861 | AATTATCCTTAGGCT[A/G]TATCATGGTTTCTGT | 9169 |
rs117725696 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923830 | GGGATTACAGGAATG[C/T]ATCACCGCGCCTGGC | 9169 |
rs117756664 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941234 | GAGCATCTCTATGGT[C/T]GTAGACACCTTACTT | 9169 |
rs117796190 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940991 | TGTATTTTTTGTAGA[A/G]GTGGGTTTCGCCACG | 9169 |
rs117850681 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945920 | TGGTCTCAAACCCCG[G/T]ATCTCAAGCGATTCT | 9169 |
rs117882904 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984686 | CTTTTGACTTGCTCT[C/T]CGCACTTCCTTTTTT | 9169 |
rs117914867 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958726 | GGGCCATGAAGGCTA[C/T]CACAGGTTCACCCTG | 9169 |
rs118114840 | snp | C/T | 0.0437048 | 0.141217 | missense | SCAF11 | GRCh38.p7 | 12:45928653 | ATGGATTACTGTTAC[C/T]TGGGGCATCACACCC | 9169 |
rs137864097 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920037 | AGGTGTGCCTTGATA[C/T]TCTGAAACACTGTCT | 9169 |
rs137874796 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952530 | TTTCAAATTGAGTTA[C/T]AGGTGCTCTTTATTT | 9169 |
rs137901313 | snp | G/T | 0.000774077 | 0.0196581 | missense | SCAF11 | GRCh38.p7 | 12:45927363 | TGGTTTTATCTATGG[G/T]ATCTTTTGGGCTTTC | 9169 |
rs137925315 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986803 | TTAACAGATGTTTCC[A/G]CTTTTGCATCTTCCT | 9169 |
rs137971738 | snp | A/C | 0.00779006 | 0.0619439 | missense | SCAF11 | GRCh38.p7 | 12:45927093 | TTTCCCTAGTAGTAT[A/C]CCTTTTTGGAGACCG | 9169 |
rs138019836 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957891 | GGGAAATAATGATTC[C/G]TACTTTCTCTCTTTT | 9169 |
rs138051342 | snp | A/C | 0.000153988 | 0.00877328 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45925022 | TTGCATCATATTTAT[A/C]GGTAGCTGAGAACCA | 9169 |
rs138069688 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920957 | AGATACTATGAAAGA[A/G]CATAATTTCTACAAA | 9169 |
rs138069842 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972876 | TATCGATATATATAT[A/C]TATAGATATATATAT | 9169 |
rs138200009 | snp | C/T | 0.00159617 | 0.0282053 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991524 | CCGAGATCGTTCCAC[C/T]GCACTCCAGCCTGGG | 9169 |
rs138228362 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936627 | AAAACTCTTTCTTTG[C/T]CCTGGTCCAATATGA | 9169 |
rs138256425 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986011 | TTCTCTGATCTTCAC[A/C/G]GTATTCTCTGGGAGC | 9169 |
rs138292713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967883 | TCTGTTCTATCTGCC[C/T]GGACTCCAGTTTTCA | 9169 |
rs138317780 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941571 | CTCCCTATCTTCCCC[A/G]CTCCCAAAAACCACC | 9169 |
rs138338638 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976445 | TAAACTTTATCATGA[C/G]TATGTACATATAGGA | 9169 |
rs138357286 | snp | C/T | 0.000230734 | 0.0107384 | missense | SCAF11 | GRCh38.p7 | 12:45928142 | TTTTCCAATGGATCA[C/T]CTCCTTTTTCAAGAA | 9169 |
rs138367681 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991097 | CGGTGGATTGAGTGT[C/T]CACCTGGCTGCGCTG | 9169 |
rs138452046 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952010 | GAAAGATGAGTTGGG[C/T]TGACAGCAGTAGTTC | 9169 |
rs138471442 | in-del | -/ATCGTTTCACAA | 0.417521 | 0.185571 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935889 | TGTGGTTTCCTGAAG[-/ATCGTTTCACAA]ATCCACCCTACTTGT | 9169 |
rs138527613 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972950 | TATAGATATATATAT[A/C]GATATATAGATATAT | 9169 |
rs138576816 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948040 | TGGTCTAAAACAGAT[C/T]CAGAAATAAACTGAA | 9169 |
rs138601301 | snp | A/G | 0.00080695 | 0.0200705 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926263 | TCTCACGGCCCAGCT[A/G]GATGCAGATGTCCAT | 9169 |
rs138613821 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963777 | TAGTGAAAATTAAAT[C/T]AGCTTTAGAAGCAGA | 9169 |
rs138631830 | snp | A/G | 0.000263639 | 0.0114782 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927307 | GGGTGACCAAGTTGT[A/G]GATGGAGAATGAAAT | 9169 |
rs138633621 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966746 | TCAAGGAACAACAAC[A/G]AAGAGATGAATGACT | 9169 |
rs138690165 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957169 | TACATTTACATTACC[A/G]TTCACAGAGAGCTAC | 9169 |
rs138790986 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45975842 | CTGTCTTATATGGGC[A/G]CTCTTCGTGGTGCCC | 9169 |
rs138904984 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953042 | GGGCTGAGTTACTAT[A/T]TTCTTTCTCTTTTAA | 9169 |
rs138922012 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947682 | TAAGCATTCAGAATT[G/T]TGGTTTGTTTTTGAG | 9169 |
rs138931697 | snp | A/T | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981221 | TGTTCACCATGACTA[A/T]CACAGGATATGATTT | 9169 |
rs138984531 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940729 | TCTAAAACAGTTTCA[C/T]CGCATTGTATCTCAA | 9169 |
rs138994649 | snp | G/T | 0.000153988 | 0.00877328 | missense | SCAF11 | GRCh38.p7 | 12:45924927 | TTCATCAAAGGAGCA[G/T]GAACACCCACTGGAT | 9169 |
rs139056670 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982923 | GTACAAGGAGTAGAC[G/T]TGGAGACATAGGATA | 9169 |
rs139078201 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937701 | TCCTACTTTGGAAAA[G/T]TATAATAATCAAGAC | 9169 |
rs139097008 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978181 | ACAACTGTAAACAGT[A/G]GCATATGTCCTTTGA | 9169 |
rs139174627 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938732 | ACAAACAAGTATAAT[A/C]AAGGCTCTGAGCTTA | 9169 |
rs139189148 | snp | C/G/T | 0.00676609 | 0.0577691 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943019 | ATCTAATACTGAGTA[C/G/T]GTATTGAGTATGAAT | 9169 |
rs139276666 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929401 | GAGTTCAAGTGATCT[C/G]CCTGCCTCGGCCTCC | 9169 |
rs139297971 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45990092 | CAGAGAGGCGGCGGC[-/G]GGCCCAGGGCCGGGC | 9169 |
rs139303867 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950445 | ATACAAACTCTATCA[A/T]ATAAATTTTATTCTA | 9169 |
rs139334838 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934923 | GGTAGCTATCTCAAG[C/T]AGGGGCTGACTAGGT | 9169 |
rs139363525 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935334 | AGCTGTTTGGTTTTG[C/T]ACAAGTCCCTCTCAG | 9169 |
rs139476507 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964005 | AATTTAAGAACAACA[A/G]TAACAAAAAACTCCT | 9169 |
rs139512685 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977468 | GCGGGGGTGGGATGA[C/T]AGAACCATTGCAAAT | 9169 |
rs139518332 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959373 | ACGTACTTAAAAATC[G/T]TAAGTTTAGAATCCT | 9169 |
rs139549576 | snp | C/T | 0.00597247 | 0.0543191 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990765 | GCCGCAGGGGGGCGC[C/T]GGCAAACTGCTGTTT | 9169 |
rs139559188 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969742 | AGAGTGTGAGTGTGT[C/G]TGTTTGTTTTAAGAG | 9169 |
rs139620500 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983480 | TACCAGAACACGATA[C/T]ATTTAAAAAATTAAA | 9169 |
rs139671527 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984114 | TGCTCATGTTACGAA[C/T]AGTGAGGGAACCCAG | 9169 |
rs139674349 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954557 | TTATGACAGTTTTAA[C/T]CTAAGCTGTTACTTT | 9169 |
rs139696403 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968759 | TAGCCTGACCAACAC[A/G]GTGAAACCCCGTCGC | 9169 |
rs139799869 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942445 | TTCCCTTCACAGCCA[C/G]AGTAATCCTTTTAAA | 9169 |
rs139819320 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939630 | TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC | 9169 |
rs139826670 | snp | A/G | 1.65307e-05 | 0.0028749 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45922159 | CAGATTTGCCACTTT[A/G]GTAGAATTTACTTCT | 9169 |
rs140008917 | snp | A/G | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921627 | CTTTCTATAATTAGA[A/G]GGAAAAAATCATAAA | 9169 |
rs140019814 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959752 | ATTCACTTATAATTT[A/G]TAATAAGCAATTTAT | 9169 |
rs140021707 | in-del | -/TTTT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930441 | AGGTTTTGCGTTGTG[-/TTTT]GTTTTTTTTTTGTTT | 9169 |
rs140049088 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968875 | AGGTTGCAGAGAGCC[A/G]AGATCATGCCATGGC | 9169 |
rs140085157 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965382 | CCTGGCCTAAAAGAC[C/T]AGGAAAATGGTGCTT | 9169 |
rs140152169 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952077 | CACTCCAAATGGCTC[C/T]GAAAGGTTCCTCACA | 9169 |
rs140303235 | snp | C/T | 0.084728 | 0.187577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936393 | GTGATCCACCCACTT[C/T]GGCCTCCCAAAGTGC | 9169 |
rs140332895 | snp | A/G | 1.65042e-05 | 0.0028726 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928018 | ACAAGATACAGGTTG[A/G]TACACTTTGCTTTCA | 9169 |
rs140357238 | in-del | -/AT | 0.0197687 | 0.0974348 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936670 | CAAAGCTGCTGTTCA[-/AT]AGTCATTTTGGGATT | 9169 |
rs140379757 | snp | C/T | 8.23716e-05 | 0.00641709 | missense | SCAF11 | GRCh38.p7 | 12:45928743 | GTGTAGACCTCCTTG[C/T]AGGAGTTGTCATTGC | 9169 |
rs140394710 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974896 | CAGCTGTAGCCTTAT[A/G]AAATGTATTTCTAAC | 9169 |
rs140432227 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971114 | CATTTATTTAGAAAG[C/T]TCATCAAGTGTTCTA | 9169 |
rs140469740 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950084 | AAGAGAAGGATGTTT[C/T]AGAAGCCGAAGGAAT | 9169 |
rs140493845 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980539 | AGCAAGTGATGGAGC[C/T]GGGACTGAAATTCAG | 9169 |
rs140507560 | snp | A/G | 0.00398564 | 0.0444627 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993742 | CGAGATGGCGCTACT[A/G]CACTCCAGCCTGGGT | 9169 |
rs140509615 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945061 | AAGAGGAGCAAGAAG[A/G]AAAAAAGGGGCAGAA | 9169 |
rs140712427 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969920 | TTTTTTTTCTTAAGA[C/T]GGAGTCTCGCTCTGT | 9169 |
rs140716627 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955450 | CCACCACACCCGGCC[C/T]AGACTGGCCTAATTT | 9169 |
rs140735876 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951975 | AGATATGCTGCCCGG[C/T]TGAGAACTACTAGTA | 9169 |
rs140780770 | in-del | -/AAAACC | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961871 | CCTGTTAAAGTAAAA[-/AAAACC]CAGCCATATGTGCTT | 9169 |
rs140805444 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988551 | AGTTTCGATCTTAAC[A/G]CACTAGCCCTATTAC | 9169 |
rs140813296 | in-del | -/TG | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976705 | TCCATATTTAAAATA[-/TG]TGAGATGTAGCAAAA | 9169 |
rs140841366 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975474 | GCAGCTTCCGCATCA[C/T]CACTTGCTGCTTCGC | 9169 |
rs140862415 | snp | C/T | 0.00398564 | 0.0444627 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990960 | CCTTTGGCAGTTTTA[C/T]AGGCTGCGTCGCGGA | 9169 |
rs140891748 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929876 | ATACAATATAGTCGA[A/C]CCTTTAACAACACAG | 9169 |
rs140930999 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923806 | TTGAGCCTCAGCCTC[C/T]GAGTAGCTGGGATTA | 9169 |
rs140958548 | snp | C/T | 1.64838e-05 | 0.00287083 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928444 | TTGGTGCTCTTTTTC[C/T]AACACAGGTGATGTG | 9169 |
rs141093875 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947400 | AGCAACTAAAAAAAA[C/G]AAACCTGTATATTTA | 9169 |
rs141112717 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935819 | TCTCAGGTAATTACT[C/G]AACAGCTTCAATGGC | 9169 |
rs141147254 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930996 | TCAACTGTATTATTA[G/T]AGTCATCACGTTTCA | 9169 |
rs141158904 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942483 | AGATCACGTTACTCC[C/T]GAAAACACTCCCTAG | 9169 |
rs141229062 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919628 | TGTATTTTTTCAACA[C/T]AAAGCATGCATTTTC | 9169 |
rs141234403 | in-del | -/GG/GGG | | | frameshift-variant, cds-indel | SCAF11 | GRCh38.p7 | 12:45928708 | TGAGACTGACTGGCT[-/GG/GGG]GTTTCAGCTCTTGTG | 9169 |
rs141265124 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965906 | AGCAGAAGAAACTTA[G/T]TAGCATATGTAAGAA | 9169 |
rs141300912 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987729 | GAGCCTTGTAGACCA[C/T]AGGAGTATGGAATTT | 9169 |
rs141375692 | snp | C/T | 0.00438332 | 0.0466095 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920720 | TAGAATTTTGCAACA[C/T]GGCTAATGGCTACCA | 9169 |
rs141444053 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | SCAF11 | GRCh38.p7 | 12:45924955 | GATATGGGAAGATAT[C/T]CATAGGCTGGTGTTG | 9169 |
rs141457242 | snp | A/C | 0.00119737 | 0.0244387 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990523 | GAGGCGGCGGCGAAG[A/C]AGGGAGCGACCCAGG | 9169 |
rs141484476 | snp | C/T | 0.000479271 | 0.0154728 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927988 | CTCTACATTCTCAGA[C/T]AAGTCACTTAGGGGA | 9169 |
rs141512061 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977390 | TTACATGCAAACCTA[C/T]AGTGATGAAGAACTT | 9169 |
rs141567863 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940897 | CAGCCTCAACTTCCC[C/T]AGGCTCAGGTGATCC | 9169 |
rs141585724 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981559 | TCCTTGAATAAATAC[A/G]TTTTTGTTTTTTATC | 9169 |
rs141591603 | snp | C/T | 4.94352e-05 | 0.00497143 | missense | SCAF11 | GRCh38.p7 | 12:45926346 | TATAGGATTGCTGTT[C/T]CACAAACTTGAAAGA | 9169 |
rs141665011 | snp | A/G | 8.24205e-05 | 0.00641899 | missense | SCAF11 | GRCh38.p7 | 12:45928065 | GAAAATCATTTGGAA[A/G]ATGAACTGTACATAC | 9169 |
rs141679072 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977744 | AAGGCACCCAAATTA[C/T]ACTGCCACAAGATGA | 9169 |
rs141679895 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946151 | CTCACTCAGTTACCA[C/T]TCTCTACAATGACTT | 9169 |
rs141761208 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967371 | TTAATGGCCAGGTGC[C/T]GGTGGCTCACGCAAG | 9169 |
rs141761795 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948882 | GTCTTAAAGGATAGT[A/T]AGGAATTGGTCTAAG | 9169 |
rs141804184 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963356 | AAAAGCAGAAAATTG[C/G]AAAAGACAGATCACC | 9169 |
rs141916468 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968122 | TGGCTTTATAATCAT[A/G]TTATATTCTACCTAT | 9169 |
rs141952164 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938420 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTAAG | 9169 |
rs141978489 | snp | G/T | 4.96044e-05 | 0.00497993 | missense | SCAF11 | GRCh38.p7 | 12:45927647 | TCGGTCAGCGATTCA[G/T]TCTTTTCTTCTAAAG | 9169 |
rs142000436 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963798 | TAGAAGCAGAGGACA[A/G]TACCAACGCTAACTT | 9169 |
rs142094403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956986 | TGGATCTGAAAAAAT[C/T]AGCTACAAGTTAAAG | 9169 |
rs142134908 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930222 | GAATTAAACTTCTTC[C/T]TATAAAGCCATAATT | 9169 |
rs142155381 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980187 | GCAATTTACCAACAA[A/G]TAACACAAATATTAA | 9169 |
rs142314830 | snp | A/G | 0.00478085 | 0.0486577 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993965 | TTCAAAGGACATACT[A/G]TCTGAGCAACATAGT | 9169 |
rs142354608 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980860 | TTCCAAAATACCTGT[A/G]TTTGGGAGGAGTGTT | 9169 |
rs142403222 | snp | C/T | 4.94295e-05 | 0.00497115 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924905 | GTTAAATGGATTGCG[C/T]TGGATGTTCATCAAA | 9169 |
rs142422298 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940051 | CTAAACTTTGCAATA[A/T]TTCCAAGTTACACTT | 9169 |
rs142445862 | snp | C/T | 1.64944e-05 | 0.00287175 | missense | SCAF11 | GRCh38.p7 | 12:45927045 | TCTCTCTAGAAGTTT[C/T]TCTTCTTGGGGACAG | 9169 |
rs142462169 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985120 | ATTTAGAAAACAAGA[C/T]TTGGATGCTCTAATT | 9169 |
rs142472430 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937087 | ATATTATTTCTTCAT[A/C]TCTGGACACCTGTGC | 9169 |
rs142478987 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965111 | ATGGATCGCTAATGA[C/T]TGACTGAGAACCTTA | 9169 |
rs142505982 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987448 | TGTTCAGGTGTTTAG[C/G]TGACAAATACTGACA | 9169 |
rs142586488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969799 | TGGAGCGTGGTGGCA[C/T]AATTACAGCTCACTG | 9169 |
rs142609275 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939940 | ACTAACTCTACCTTC[A/G]TGACTTTGTCTCTTG | 9169 |
rs142744626 | snp | A/C/T | 0.0115267 | 0.0751584 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964699 | AGGAAAAGCCTTTTA[A/C/T]AACTATTAAGCAACA | 9169 |
rs142772617 | in-del | -/CCCC | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990678 | AGGTGACGACGGCGG[-/CCCC]CAGCCGGACTCGCCA | 9169 |
rs142823846 | snp | A/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920964 | ATGAAAGAACATAAT[A/T]TCTACAAAGTCAACA | 9169 |
rs142844694 | snp | A/C/T | 3.29614e-05 | 0.00405951 | missense | SCAF11 | GRCh38.p7 | 12:45928590 | ACTTCCGTTTTGGAG[A/C/T]CTGTCTTGTTTGCTT | 9169 |
rs142847427 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954374 | CCTGAGTAGCTGGGA[C/T]TACAGGTGCATGCCA | 9169 |
rs142888739 | snp | A/G | 0.000131857 | 0.00811855 | missense | SCAF11 | GRCh38.p7 | 12:45924829 | GAGATACACTGGTAG[A/G]AGTGGCTACCTGCAT | 9169 |
rs142941606 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953206 | TTCCCTATAGAAAAC[G/T]TGACCTTAAGAAGGT | 9169 |
rs142972262 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986040 | GCTCACATTCTTCCA[C/G]CAAAGTTTTTTAAAT | 9169 |
rs143001172 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923743 | GCTGGAGTGCAGTGG[C/T]GCGATCTTGGCTCAC | 9169 |
rs143171540 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920374 | ATTGCTCTGGCTAAA[C/T]AGTTTAGCTAGTAAA | 9169 |
rs143187024 | snp | C/T | 3.30808e-05 | 0.00406686 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45922541 | AAATGGCTTGATGGC[C/T]AATTTTACCTCTTGT | 9169 |
rs143191439 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966698 | GGCAGAGAGAATAGC[C/T]AATATGAAAGTCCTA | 9169 |
rs143232826 | snp | C/T | 0.000395537 | 0.0140575 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928504 | ATCATTGGAAGATGA[C/T]TTTTCAGGGGCAGCT | 9169 |
rs143273826 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938245 | CTGTAATCCCAGCAC[C/T]CTGGGAGGCCGAGGT | 9169 |
rs143362270 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934949 | TAGGTGGCCTGGGGC[A/C]ATCAGCTCTTGTTAA | 9169 |
rs143478424 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956476 | CAAATTAATTGTTCA[C/T]CTGCAGTCAGCCTAC | 9169 |
rs143526998 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936345 | TGGGGTTTCACCATA[C/T]TGGTGAGGCTGGTCT | 9169 |
rs143572940 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954817 | TCTTGAACTCCTGTG[C/T]TCAAACGATCCTCCT | 9169 |
rs143585659 | snp | C/T | 0.0279526 | 0.114869 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962294 | GAATACTATACACAC[C/T]AGTCTGCTTTTTTCT | 9169 |
rs143615919 | snp | A/T | 0.00672032 | 0.057576 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927148 | TGCAATATCCTTTTT[A/T]GGGGACTGAGAACGG | 9169 |
rs143643099 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946699 | TATGAGTTGTATCAA[C/G]AATTAAAAGTATTTC | 9169 |
rs143716403 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932861 | ATGTATTACTAACAA[C/T]AAATCTTAATATTCG | 9169 |
rs143749008 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958817 | TTTAAAGTCCTTACA[C/T]AGCTTTTGTTTAAAT | 9169 |
rs143757539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981269 | TATATCAGTAAGACA[C/T]GTTAATGAGAAAGGA | 9169 |
rs143770928 | snp | C/T | 0.00358779 | 0.0422022 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992854 | TTTCCTAGCAGAGAA[C/T]TAAGTTTTCACGTTC | 9169 |
rs143856565 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934598 | GCACATTGGCAAGGG[C/T]TGAAATACGTAGAAA | 9169 |
rs143857988 | snp | A/C | 1.64792e-05 | 0.00287042 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927493 | AAGATCAGCATTTAC[A/C]GATGGTTCAACTTCA | 9169 |
rs143868395 | snp | C/G | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987559 | ATGATAAATGCAATG[C/G]AGAAAAATCTAGCAT | 9169 |
rs143875430 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951099 | AAATCATAATCATGG[A/C]TCACAACAGTAAGTA | 9169 |
rs143965074 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973915 | TAAATGCCTGAGCAA[A/G]CATAGTTAACTATTC | 9169 |
rs143979547 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935506 | AAAATGTGTGGTAGG[A/T]ACACAGATAACACTC | 9169 |
rs144007389 | snp | G/T | 0.000153988 | 0.00877328 | missense | SCAF11 | GRCh38.p7 | 12:45926223 | GTCGTGAGTAGTAGT[G/T]TTGTACATCTGCTGG | 9169 |
rs144055349 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929742 | TACAACATGATGTTT[C/T]GAAGTACATATACAT | 9169 |
rs144056053 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976853 | AAGGAACAGAAATCA[A/G]TGAAATTGGAAACAG | 9169 |
rs144074897 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958014 | CCTCCAACCTCCCCC[C/G]ATCAGCTTCCCAAGT | 9169 |
rs144133922 | snp | A/T | 0.00795532 | 0.062565 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978377 | ACCTAAAGCTCTCTT[A/T]TATTTATTTCCGCCA | 9169 |
rs144145801 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973295 | TTGAAAAAAAAATAT[C/T]AAAGGCTTAGGGACC | 9169 |
rs144154919 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975073 | GTTGAAAGGAATCTT[C/T]TTATCTGAGCATTTG | 9169 |
rs144211372 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942592 | ACTAACTTCCTTGCT[-/A]TTCTTTGGAGACATT | 9169 |
rs144247252 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964762 | TAAATGCAATTGAAG[C/T]TTAAGGAACAGAGAT | 9169 |
rs144389375 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950124 | GTCAGCAGCACTACA[C/T]GCAGAAAACAAACCA | 9169 |
rs144474708 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959405 | GTCTTGTATAGCAAA[C/T]AAATATTAACATAGT | 9169 |
rs144505714 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935454 | ATCTAAAAGATGATA[C/T]GCTGATTTTTTAAAA | 9169 |
rs144553348 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955476 | AATTTTAAGGAACTC[C/T]CAAGGATGCCTCACT | 9169 |
rs144691936 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945982 | AGGCATGAGCCACCA[A/C/T]GTCTGGCTTCATCTC | 9169 |
rs144698303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922859 | ATTCCCTTCACCACT[C/T]ATACAATAAAAAGCT | 9169 |
rs144756998 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931223 | TCCAGGTTCATCCAC[C/G]TTGGCACAAACAAGA | 9169 |
rs144839979 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929991 | TTACTGATAACAGTG[A/G]ATTAATATATTTTTT | 9169 |
rs144878744 | snp | A/C/T | 4.95703e-05 | 0.00497826 | missense | SCAF11 | GRCh38.p7 | 12:45927992 | ACATTCTCAGATAAG[A/C/T]CACTTAGGGGACAAG | 9169 |
rs144921278 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966520 | TGGAGAAAAATTAAA[A/C]ACAGTGTGGCTATTA | 9169 |
rs145032474 | in-del | -/GA | 0.215747 | 0.247642 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942964 | ATTTGTTAAATGTAT[-/GA]GAGTGATCTCAATTC | 9169 |
rs145035405 | snp | C/G | 0.00167915 | 0.0289267 | missense | SCAF11 | GRCh38.p7 | 12:45927341 | GATCTTCGAGTACGA[C/G]GCTTTTTGGTTTTAT | 9169 |
rs145082757 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924179 | GCAGTCATAAAATTA[A/T]AAGCAACAAATTGTT | 9169 |
rs145107918 | snp | A/G | 0.00199481 | 0.0315187 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990526 | GCGGCGGCGAAGCAG[A/G]GAGCGACCCAGGTTG | 9169 |
rs145127097 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986310 | GGTCCTTATCTGGCA[A/C]AACCCAGGAATGTAA | 9169 |
rs145295131 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955955 | ATGCTCTGTACTAAG[A/G]TTGTTGTATCAGTTA | 9169 |
rs145376945 | snp | A/G | 4.94678e-05 | 0.00497307 | missense | SCAF11 | GRCh38.p7 | 12:45928046 | TCAGATGTTAAACAT[A/G]TAGGAAAATCATTTG | 9169 |
rs145422545 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984482 | ACTTTGATAACTTGA[C/T]TGAGGTAATATCATC | 9169 |
rs145446909 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972779 | TAAAAGAAAACACCA[C/T]CAAGATGATACAGCT | 9169 |
rs145470245 | snp | C/T | 0.00060941 | 0.0174452 | missense | SCAF11 | GRCh38.p7 | 12:45928755 | TTGTAGGAGTTGTCA[C/T]TGCAGGTTTTCGTCT | 9169 |
rs145483884 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926019 | TAAGTGACTTGTAAA[C/T]AACTAAGGTTCAGCT | 9169 |
rs145488488 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967675 | GCTTTAAAAACTGTT[C/T]AAGCATTCCAAAGTT | 9169 |
rs145527294 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930912 | ATCTCCAAACATTTT[C/T]CGATATATTTATTTT | 9169 |
rs145538518 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969374 | GTTTCTTTCTGCTGT[C/T]ACAAAACAGAGCTCC | 9169 |
rs145545437 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983990 | ATTTTCACTAAAAGT[A/G]TTGGTATAATAATCT | 9169 |
rs145570738 | snp | A/G | 1.6537e-05 | 0.00287545 | missense | SCAF11 | GRCh38.p7 | 12:45926567 | TTTTCTTCCCAATGA[A/G]ACTCTTTCAACTTTT | 9169 |
rs145648362 | snp | A/C | 0.00993419 | 0.0697739 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939733 | AACAAATAAATAAAT[A/C]AGAAAACAAGAAGCT | 9169 |
rs145678768 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989153 | ACAATTACTAATAAA[A/T]TACAAAAACCAACCG | 9169 |
rs145757842 | snp | C/T | 0.00267866 | 0.0364987 | missense | SCAF11 | GRCh38.p7 | 12:45927833 | TTAACAGATTGTCTG[C/T]CCACTGTCTGTATAA | 9169 |
rs145763484 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957030 | AGCAATCACTCCAAC[C/T]CACACTAAGGATGAA | 9169 |
rs145774568 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951990 | TTGAGAACTACTAGT[A/G]TAGTGAAAGATGAGT | 9169 |
rs145837982 | snp | C/T | 1.64776e-05 | 0.00287028 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923100 | GGGCTGCTGTCGGAG[C/T]AGGCAAAACTGGTGT | 9169 |
rs145838012 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960757 | CATTCTCCTTTCCAC[A/T]CTATTAATGAAAATT | 9169 |
rs145879376 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961031 | TATTTGGCCCAAATT[A/G]AGTCAACATAATACA | 9169 |
rs145937460 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939589 | TGTAATCCCAGCTAC[C/T]TGGGAGGCTGAGACA | 9169 |
rs146076146 | in-del | -/GT/GTGT | 0.185155 | 0.241444 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964928 | TGTGTGTGTGTGTGT[-/GT/GTGT]CTACTAAGGAGACAG | 9169 |
rs146091932 | snp | A/T | 0.00597247 | 0.0543191 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921143 | GCCCACCACCACGCC[A/T]GGCTAATTTTTGTAT | 9169 |
rs146170847 | snp | A/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977808 | GCTTTCTCCATTTCT[A/T]CAGCACTGACAGTTC | 9169 |
rs146172345 | snp | C/T | 0.00116889 | 0.024147 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923022 | CAGCATTAGAGGCTT[C/T]GCTGTGACTTGATGA | 9169 |
rs146183261 | snp | C/T | 0.000264271 | 0.011492 | missense | SCAF11 | GRCh38.p7 | 12:45926489 | CCTCTGCCTCTACCA[C/T]GGTTAGATACCCAAC | 9169 |
rs146210628 | snp | G/T | 0.000774089 | 0.0196582 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927361 | TTTGGTTTTATCTAT[G/T]GTATCTTTTGGGCTT | 9169 |
rs146219962 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982424 | AAAAATCACCTATCG[G/T]GGCCGGGTACAGTGG | 9169 |
rs146242023 | snp | C/T | 0.0154538 | 0.0865337 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920931 | ATTTATCGTCTGCAA[C/T]GGGTAGAAGAAGATA | 9169 |
rs146299748 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959162 | CTTATGCAGATTTCT[C/T]AGGAGCTGTGGCACA | 9169 |
rs146338908 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963931 | AATCAAAAAACTTGA[C/T]CAGTCGAAAATAAGA | 9169 |
rs146355113 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985149 | TTATTTCAATGTCTA[C/T]GTGTAGAAAACCATG | 9169 |
rs146355168 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937308 | ATATTTTTAACTTCT[A/G]AAAGCTTTTTCTTAA | 9169 |
rs146384068 | in-del | -/A | 0.0737376 | 0.17729 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963466 | TCAAAGTGCTAAGAG[-/A]AAAAAAAACTATCAT | 9169 |
rs146401933 | snp | C/G | 0.000280082 | 0.0118306 | missense | SCAF11 | GRCh38.p7 | 12:45924914 | ATTGCGTTGGATGTT[C/G]ATCAAAGGAGCATGA | 9169 |
rs146430873 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935789 | CAAAAGCTGTTTCAC[A/G]TATTTCTGGGTAATT | 9169 |
rs146472137 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975295 | AGACAGTCAGCCTGT[A/C]CTTGGAAGCTTTGAA | 9169 |
rs146521032 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930923 | TTTTCCGATATATTT[A/G]TTTTTTAAAATTCAT | 9169 |
rs146521243 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978599 | CTGTATTTTCACATC[A/T]GGGAGGCAGAATAAC | 9169 |
rs146566679 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940136 | AACCTCATAAGAAAT[A/G]TGAAAATTAAAAGAA | 9169 |
rs146678365 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974658 | TCCACTTCTAATTCT[A/G]TAATAGTTCTCCTGC | 9169 |
rs146737902 | snp | C/T | 0.00119737 | 0.0244387 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928009 | ACTTAGGGGACAAGA[C/T]ACAGGTTGGTACACT | 9169 |
rs146750023 | snp | C/T | 6.58968e-05 | 0.00573969 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928741 | ACGTGTAGACCTCCT[C/T]GTAGGAGTTGTCATT | 9169 |
rs146751109 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970797 | AGCTGAAGTCACCCA[C/T]ATTTACAGGTCTTTT | 9169 |
rs146879188 | in-del | -/TTA | 0.0107246 | 0.0724382 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938927 | CCCAAACCAAAGATT[-/TTA]AATGTTCATTCCAAG | 9169 |
rs146883801 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951947 | GACAGAATCTGTTAT[C/T]AAAATCCCATTAAGA | 9169 |
rs146895371 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981035 | CAAAATAAAGAAATA[C/T]TGTCAAAGAGTATAT | 9169 |
rs146968172 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919637 | TCAACATAAAGCATG[C/T]ATTTTCTAATACATT | 9169 |
rs146979342 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932041 | TACCAAAGTGTGTGC[-/AT]ATATATATATATATG | 9169 |
rs147035575 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976437 | TTATAAGTTAAACTT[A/T]ATCATGAGTATGTAC | 9169 |
rs147065386 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980574 | TCAGGCTCCCTTATG[C/T]TCTTAACCATTGACA | 9169 |
rs147148405 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952887 | TTCCTATGTAAAAAA[C/T]GTGATCTTTGCCTTT | 9169 |
rs147181321 | snp | A/G | 0.0158469 | 0.0875917 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993573 | AGGTCAGGAGTTCGA[A/G]ACCAGACTGGCCAAC | 9169 |
rs147204397 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988365 | AGTTGATGGGTAGTA[C/T]AGTACTGTATTTTCT | 9169 |
rs147224513 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949093 | AGTGAATGCGATGAT[C/T]AAATTTGTTTTTAGG | 9169 |
rs147297404 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973409 | TAGAAAGAAGAAGAA[A/G]AAGAAGAAGAAGAAG | 9169 |
rs147306639 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969496 | CCTGGTTAATACTAC[A/C]AACTTTAGAATCCAA | 9169 |
rs147316968 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934608 | AAGGGTTGAAATACG[C/T]AGAAAAGCTGTATTT | 9169 |
rs147324041 | snp | A/G | 0.000362605 | 0.01346 | missense | SCAF11 | GRCh38.p7 | 12:45928277 | TGAGCACAAGACTCA[A/G]AAGATGAAGATCCTA | 9169 |
rs147326720 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929760 | AGTACATATACATTG[C/T]GGAATGACCAAATCT | 9169 |
rs147327182 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976972 | TAGCCTGAATAGCCT[C/T]AGGACTATTTGAAGA | 9169 |
rs147402032 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953785 | TTACAGTCTCTCTGT[A/G]CCTCAGTAACCTTAT | 9169 |
rs147432329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957867 | TTTTAATCACTTCTC[A/G]GCAACTGTGGGAAAT | 9169 |
rs147499819 | snp | A/C/G | 6.59265e-05 | 0.00574104 | missense | SCAF11 | GRCh38.p7 | 12:45928521 | TTTCAGGGGCAGCTA[A/C/G]AGAGCTCCGAAGTTT | 9169 |
rs147594863 | snp | A/C | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924208 | TTTGCAAATTATTCA[A/C]ATTTTCTATGTCTCA | 9169 |
rs147603901 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944534 | GTTCTAGCTGTAAGT[A/G]GAAATTCACTGTGAC | 9169 |
rs147656077 | snp | C/G | 0.0142736 | 0.0832652 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980624 | AAAGGATCTCTATAA[C/G]GGTCATAAGTTACCC | 9169 |
rs147698283 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985005 | CAGCCACTTCCTTAC[G/T]TTTGGACATAAGAAA | 9169 |
rs147710939 | snp | C/T | 0.000247099 | 0.0111125 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926860 | TGAACTCTTACTTTT[C/T]GTTCTACATCTTGAG | 9169 |
rs147717714 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923768 | GCTCACTGCAATCTC[C/T]GACTACCAGGTTCAA | 9169 |
rs147727215 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919425 | TTAGTCTCAAAATTC[C/T]AGGCATTTCTATAAA | 9169 |
rs147759588 | snp | C/T | 0.000132705 | 0.00814463 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961304 | AAAGAAGAAATCAAA[C/T]AACCTATGTGAAAAG | 9169 |
rs147802299 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965525 | TGCTGTGTTTCCCAG[A/G]CTGGTCTCCAACTCC | 9169 |
rs147830812 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950247 | AGTAAGAATTGAGAA[C/G]AGGTAGTTGTAGAAT | 9169 |
rs147845633 | in-del | -/AAAC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978898 | ACAAACAACAAATAA[-/AAAC]AAACAAACAAACAAA | 9169 |
rs147889936 | snp | C/T | 1.64928e-05 | 0.00287161 | missense | SCAF11 | GRCh38.p7 | 12:45927122 | CGAGACTGAGATTGC[C/T]TCCTTTCTCTTGCAA | 9169 |
rs147906788 | snp | A/C/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946106 | GACCATTAGGAAATT[A/C/G]TAGCAAAGAAAGCAT | 9169 |
rs147937340 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930065 | AAGAAAAGGTTATTA[C/T]AAAAATCATAAGAGA | 9169 |
rs148002695 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956560 | ATTAGTGAAACTGTG[A/G]TTCTTTATACCAGCA | 9169 |
rs148013560 | snp | C/T | 8.24273e-05 | 0.00641926 | missense | SCAF11 | GRCh38.p7 | 12:45928059 | ATGTAGGAAAATCAT[C/T]TGGAAGATGAACTGT | 9169 |
rs148056406 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962626 | CAGAAATAAAGGATT[A/G]GTCAGCTGAAATGTG | 9169 |
rs148074494 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933834 | GGATTCAAAGATGAA[C/T]GGATCAGCTGTAAAA | 9169 |
rs148142551 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981498 | AAAAGATCCAAAAAC[C/T]GAAACATCATTCTCC | 9169 |
rs148196308 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987689 | AGGAGATGAAGTCAG[A/G]GAGGAAGAAGAGACT | 9169 |
rs148224479 | in-del | -/GTAGTAAA | 0.0142736 | 0.0832652 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989819 | TCGAGAGGTCACGGC[-/GTAGTAAA]GTTTGGTTTCACTAG | 9169 |
rs148268522 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920673 | CATTATTTAAATTTC[A/C]CCTCTGTTTCTAAAA | 9169 |
rs148320367 | snp | A/G | 0.000614286 | 0.0175147 | missense | SCAF11 | GRCh38.p7 | 12:45927698 | AGAAGATTATTTTTT[A/G]GTAAGTTATTTTCAG | 9169 |
rs148344218 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977147 | AAATCATTTTATGAA[A/T]CCAGCATTATCCTCA | 9169 |
rs148361648 | in-del | -/TA | 0.117537 | 0.212022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987925 | TATGTATTGAATTTT[-/TA]TGTGTCTATGTACTA | 9169 |
rs148404978 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948657 | TTAAAAAGTGTAGTC[C/T]AAATACATATGCTTA | 9169 |
rs148458290 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954027 | TTGCAAAGTTTATGA[C/T]GTAGATGGAAATCCA | 9169 |
rs148536014 | snp | A/C/G | 4.94469e-05 | 0.00497206 | missense | SCAF11 | GRCh38.p7 | 12:45928530 | CAGCTACAGAGCTCC[A/C/G]AAGTTTCTTTTTCAG | 9169 |
rs148580642 | snp | C/T | 0.00162951 | 0.0284973 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923079 | GAACCATTCCCGTAT[C/T]TCCTGGGGCTGCTGT | 9169 |
rs148636827 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930191 | CAGCTATAGATCTCA[A/G]TCTGTTCCTATCAAG | 9169 |
rs148646686 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974048 | GGTCTAGGTCCAGAC[C/T]GGAGTAATAAAACAA | 9169 |
rs148700042 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979619 | ATTATAAAACCAAGA[C/T]AGAAAAAAGCAATTA | 9169 |
rs148738757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958422 | TTCCTAACTGAATAG[A/T]TGATAAGCTTTAGCA | 9169 |
rs148796437 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964870 | GTATGGAGAAATACA[A/G]TAACATTTAGCTAGG | 9169 |
rs148867730 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939859 | TAAATTATCCTTAGG[C/T]TATATCATGGTTTCT | 9169 |
rs148927308 | snp | C/T | 0.000153988 | 0.00877328 | missense | SCAF11 | GRCh38.p7 | 12:45927147 | TTGCAATATCCTTTT[C/T]TGGGGACTGAGAACG | 9169 |
rs148962470 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976230 | TAGACTAAAATTTTA[A/T]GTATGTATAATTCTT | 9169 |
rs148978788 | snp | C/T | 0.000103121 | 0.00717983 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924734 | AAAACATACCTGCAA[C/T]TGCTTTCCATCTGGT | 9169 |
rs149034318 | snp | C/T | 0.00557542 | 0.0525036 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920243 | CTAGCACAATCATTA[C/T]GGGACCAACATTTCA | 9169 |
rs149110091 | snp | A/C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966689 | AGCATTCTTGGCAGA[A/C/G]AGAATAGCCAATATG | 9169 |
rs149112278 | snp | C/T | 1.65897e-05 | 0.00288003 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927958 | CTCTGTTATTTTTTC[C/T]TCATTAACCACTGAC | 9169 |
rs149139857 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950864 | ACAAAGACTAACAGT[C/G]CTACCTAAAAACGGT | 9169 |
rs149196856 | snp | C/G | 0.000971817 | 0.0220219 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956197 | AGATAGCTCCTCTTA[C/G]AGAGAGAGAAACAAG | 9169 |
rs149249601 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991170 | GGAAGCCCACCTTTC[C/G]TCCTTTCTGGTGGGC | 9169 |
rs149279044 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948122 | CAGAGGAGGGGAGGA[C/T]GGTCCTCACTATGTT | 9169 |
rs149354087 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921957 | CAAAACCAAATTTCA[A/G]TCACAGTTATGTATG | 9169 |
rs149375358 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932555 | ATATAAAATAAAGTC[A/G]TAATATGTTATAGGA | 9169 |
rs149417922 | snp | C/T | 0.0505692 | 0.150756 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968863 | CCCAGGAGGTGGAGG[C/T]TGCAGAGAGCCGAGA | 9169 |
rs149443046 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981255 | CGACACCATAAAAGT[A/G]TATCAGTAAGACATG | 9169 |
rs149452001 | snp | C/T | 0.00060949 | 0.0174463 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927412 | TTCAACCTTTTCATC[C/T]GCAAGATCAGAAGAC | 9169 |
rs149461689 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952616 | TTTATTTCCTGTCCT[C/T]TTAAAATTCCTGTGC | 9169 |
rs149514400 | snp | C/T | 0.011919 | 0.0763696 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958013 | TCCTCCAACCTCCCC[C/T]CATCAGCTTCCCAAG | 9169 |
rs149653249 | snp | C/T | 1.64909e-05 | 0.00287144 | missense | SCAF11 | GRCh38.p7 | 12:45928242 | CTTCCCCTTCCTCAC[C/T]AACTAGCACAGGAAG | 9169 |
rs149663556 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45927957 | TCTCTGTTATTTTTT[C/T]TTCATTAACCACTGA | 9169 |
rs149733891 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939685 | CCATTGCACTCTAGC[C/G]TGGGCAACAAGACCG | 9169 |
rs149735856 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970769 | TGCTTACCAGATAAA[C/T]GGAAAATTAAGAAGC | 9169 |
rs149756391 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983966 | GTTTAAAGATTGAGA[A/G]CACTTTTAATTTTCA | 9169 |
rs149893066 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973727 | GGAAAAGAACTGTAA[A/G]CCTAAAATCCTCTAT | 9169 |
rs149986952 | snp | C/G | 3.3227e-05 | 0.00407583 | missense | SCAF11 | GRCh38.p7 | 12:45927923 | AAATCTTTATGTTCA[C/G]TAATTTCTACTAGGG | 9169 |
rs150019950 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950480 | AGAAAACATAATTTC[A/G]CAGAAAAATATATTT | 9169 |
rs150041756 | snp | A/G | 0.000115318 | 0.00759249 | missense | SCAF11 | GRCh38.p7 | 12:45926846 | ATTCTACCAAATGAT[A/G]AACTCTTACTTTTTG | 9169 |
rs150081845 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925961 | TAGCATTAATAATAT[A/G]CTTATGTAGATAAAC | 9169 |
rs150090658 | snp | A/C/G | 1.64822e-05 | 0.00287068 | missense | SCAF11 | GRCh38.p7 | 12:45928107 | CCTCTGATTGTGAAA[A/C/G]TCCAGATATCTGGTC | 9169 |
rs150115725 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991022 | CAGGAAGGATTTTGC[A/G]CAGGGTGTGCTCCTT | 9169 |
rs150142649 | snp | C/G | 3.30087e-05 | 0.00406242 | missense | SCAF11 | GRCh38.p7 | 12:45927260 | GGAGATGGAGACTGG[C/G]GCCGCTTCTTTTCTT | 9169 |
rs150210544 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975587 | AGCTTCCTTATCCCT[C/G]TCAGACTTCACTGGC | 9169 |
rs150291462 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966245 | CTTAAGAACATTAGC[A/C]ATTATCTTCAAATAA | 9169 |
rs150376258 | snp | C/T | 4.94588e-05 | 0.00497262 | missense | SCAF11 | GRCh38.p7 | 12:45925021 | GTTGCATCATATTTA[C/T]AGGTAGCTGAGAACC | 9169 |
rs150472869 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941355 | ACGTACACATTGTGA[A/G]AATAATCACCACAAA | 9169 |
rs150483685 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985537 | ACCCAGCTATAGATA[C/T]TTAGCAACTTCTCTG | 9169 |
rs150517492 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983335 | CTAAGCTCCCCTAGG[A/G]CACAGACCTAATAGA | 9169 |
rs150612410 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968487 | AATGGTCTAAGTTTT[A/T]AATTTTATTTATCAT | 9169 |
rs150664474 | in-del | -/T | 0.0444908 | 0.142359 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948359 | TTAAACCCCACTTCA[-/T]TTTTTTTAATACCTT | 9169 |
rs150675454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938471 | TCCAGCCTGGGTGAC[A/G]AGAGCGAGACTGCAT | 9169 |
rs150728063 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942621 | TTCCAAGAATATTCC[C/T]GTCTCAGGCTTTTAC | 9169 |
rs150804610 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987873 | GACTTTTTAGGAAGA[C/T]ATTTTTGAAAGCAAA | 9169 |
rs150875172 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935013 | TCAGGTATGTTCTTT[C/T]CTTCCAATTTTATAC | 9169 |
rs150885060 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977441 | GGGGAATGTATGACA[A/G]CACAGTTTTTGGCGG | 9169 |
rs150900606 | snp | C/T | 0.00373621 | 0.0430598 | missense | SCAF11 | GRCh38.p7 | 12:45926670 | GTTTGTCAGCAGAAT[C/T]TGGATCATCAGCATC | 9169 |
rs150921230 | snp | G/T | 0.00993419 | 0.0697739 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969905 | CCACATTCAACCATT[G/T]TTTTTTTCTTAAGAC | 9169 |
rs150991524 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940015 | TGTCTTTTCTGTTGC[C/G]TGACAGACTCATTTC | 9169 |
rs151048452 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946769 | TACTATTATCTACTA[C/T]GTAAATACAAATGCA | 9169 |
rs151112002 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989859 | GGCTTGGACGCTCGC[C/G/T]ACCAAAGTCTCCCAA | 9169 |
rs151120050 | snp | A/G/T | 0.0245254 | 0.108477 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959667 | TACATGCTTTGAAAC[A/G/T]TATCTATTTTTATCA | 9169 |
rs151132156 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930407 | ACAAATGCTCACATG[C/G]AGATGATTACATTAA | 9169 |
rs151185617 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936353 | CACCATATTGGTGAG[C/G]CTGGTCTTGAACTCC | 9169 |
rs151208020 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980293 | AATGTTAAGCTTTTA[A/G]CCTGCCTTCTTTATC | 9169 |
rs151258002 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985191 | ATTTCTCCAATTTCA[C/G]TCCGCAAGATTTGTT | 9169 |
rs151289562 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965259 | TTATAAGCAGAGATA[G/T]TTGCATAGCTAAAGT | 9169 |
rs180673142 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975179 | CATTTATAGAGCACA[G/T]AGTAGATTCAGTATA | 9169 |
rs180741978 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922735 | ATTTACTAAAACATA[C/T]CAAACATTTCTAAAA | 9169 |
rs180744087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935739 | GAAAGAACTGTTAGT[C/T]TTCTCTGAGCAATGC | 9169 |
rs180746761 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944721 | TGTATTAGAAAATCA[C/T]GTACCAGACAAAAAC | 9169 |
rs180749102 | snp | C/T | 0.00386986 | 0.0438173 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956138 | CGATTTCTAATTTCT[C/T]GCTTCCTCCTGCTGC | 9169 |
rs180754712 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964551 | AGGTGCCTGTAGTCC[A/C]AGCTGCTCGGGAGGT | 9169 |
rs180763406 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985192 | TTTCTCCAATTTCAG[A/T]CCGCAAGATTTGTTC | 9169 |
rs180959616 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949674 | TGATCTTGGTGACTA[C/G]GGCTGTGATTCCATT | 9169 |
rs180976024 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969131 | CTATTTAAAAATATA[C/T]TTAATAGCTGCACTG | 9169 |
rs180981972 | snp | A/C | 0.00358779 | 0.0422022 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992115 | CGTCGCTTTTCTGGC[A/C]CTTTCATCCTATGCA | 9169 |
rs180994300 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959792 | GCTCTCTTGTTACTG[C/T]TCAACTGAAAGGTTT | 9169 |
rs181019829 | snp | A/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940212 | AAAGGTTCTAATCTT[A/T]CAGCTATGATTTATG | 9169 |
rs181027680 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980231 | AAATCATGAGTATTC[A/G]AACAACAAGAAGTGG | 9169 |
rs181218258 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945857 | TTTATTCTTATTCTT[A/C]TTATTATTTTTTTTA | 9169 |
rs181226333 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965117 | CGCTAATGATTGACT[A/G]AGAACCTTAGATTCA | 9169 |
rs181253659 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986756 | CATACTGTTCTCATG[A/G]TAGTGAACAAGTCTC | 9169 |
rs181301155 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933340 | ACCTGGCATTATGAA[A/T]CACACTTACAAGCAT | 9169 |
rs181307457 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923585 | GCAGTAAGTTGACAG[A/G]AGAAAAAGATTAAGA | 9169 |
rs181401562 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955025 | ACAAAAACACAAAGG[A/G]AAAACAAGAAAAAAA | 9169 |
rs181469623 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993265 | AAACTGAATGTCCAC[G/T]TGGTGTGTTGCACTT | 9169 |
rs181564886 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950730 | CCTTGCATCAAGATT[C/T]ATCTGGTAAAAATAT | 9169 |
rs181630776 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934765 | CTATGTTTACAACAT[A/G]TGAGTTAAAATTCTA | 9169 |
rs181630938 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955430 | GTTGGGATTACAAGC[A/G]TGAGCCACCACACCC | 9169 |
rs181675504 | snp | C/G | 0.00372988 | 0.0430236 | missense | SCAF11 | GRCh38.p7 | 12:45927699 | GAAGATTATTTTTTA[C/G]TAAGTTATTTTCAGA | 9169 |
rs181701151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969431 | CCCTCTCCCTCCTTG[C/T]TCTTGCTGTTCTCTT | 9169 |
rs181718003 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987868 | ACAGTGACTTTTTAG[G/T]AAGATATTTTTGAAA | 9169 |
rs181836869 | snp | A/G | 0.000247107 | 0.0111127 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928675 | ATCACACCCAGAATT[A/G]TCTGATATTGGGGAT | 9169 |
rs181845954 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979990 | CAAATGCCCATAACC[A/T]AGATTTTTGTGTAAG | 9169 |
rs181849729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951108 | TCATGGCTCACAACA[C/G]TAAGTAACATTAATG | 9169 |
rs181864537 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965770 | TTCTATTAATTTCTA[A/T]AATAATTTACACATG | 9169 |
rs181908290 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959518 | TCCTGATCCTGAAAT[C/T]CGAAGTAAACTGTAA | 9169 |
rs182043584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923920 | CAGTGGTGCAATCTC[A/G]GCTCACTGCAACCTC | 9169 |
rs182074098 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970152 | ACCCGCCTTGGCCTC[C/T]CAAAGTGCTGGGATT | 9169 |
rs182108962 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974723 | ACACAAGTTTTGAAT[A/C]CCTAAAAGTCATCCA | 9169 |
rs182118031 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947018 | TAACATCTAAGGAGC[C/T]TACAGTGTTATAAAT | 9169 |
rs182118830 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957512 | AGACACTTCATTTCT[A/G]GTTTAGGAGAGAAAC | 9169 |
rs182132133 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976841 | AGGAAGAAAATAAAG[C/G]AACAGAAATCAATGA | 9169 |
rs182164452 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939860 | AAATTATCCTTAGGC[C/T]ATATCATGGTTTCTG | 9169 |
rs182245176 | snp | A/C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970933 | ATGCATGTCACCTCA[A/C/T]ACTATGCTCTACAAT | 9169 |
rs182250246 | snp | A/G | 0.00199481 | 0.0315187 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918921 | TACTAAAGTTTTTCT[A/G]ATTTCTTACAATAAT | 9169 |
rs182309123 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929731 | TGTTTCTCATGTACA[A/C]CATGATGTTTTGAAG | 9169 |
rs182320090 | snp | C/T | 1.66032e-05 | 0.0028812 | missense | SCAF11 | GRCh38.p7 | 12:45951660 | CTTACCTTAACATAA[C/T]CTTCCAATGCACTGA | 9169 |
rs182354924 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947970 | GTGTGAGCCACCACA[A/C]CTGGCCAGCATTCAG | 9169 |
rs182379336 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988583 | ACATGAAGGTATTAA[C/T]AGAAAAAATTAAAAA | 9169 |
rs182379820 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993583 | TTCGAGACCAGACTG[A/G]CCAACATGGTGAAAC | 9169 |
rs182445517 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967446 | ATCAGGAGTTCGAGA[C/T]CAGCCTGGCCAACAT | 9169 |
rs182448645 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990203 | TTTCCTCCCAGCGCA[A/C]GACGTCGCACGGGCC | 9169 |
rs182514717 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924330 | GTCTGAACAAGACAA[C/T]AAAAGCTTCATCACA | 9169 |
rs182516706 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948139 | GTCCTCACTATGTTC[C/T]CCAGGCTGGTACCAA | 9169 |
rs182632418 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966719 | GAAAGTCCTAAGGCA[C/T]GTCTGGTATGTTCAA | 9169 |
rs182774194 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971715 | ACTGCTCCTTTTTTT[C/T]TGTTTTCCCCCTTTC | 9169 |
rs182863847 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960425 | AAATCTCTAAAAAAA[C/T]TTAACCACAAAGCAA | 9169 |
rs182868562 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981725 | ACTTGAGCCCAGGAG[G/T]TTAAGGTTGCAGGGA | 9169 |
rs182908183 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942054 | TGATTTCTTAATAAC[A/G]TTCTTTCTCCAGCTT | 9169 |
rs182926617 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982971 | AGCATATGCCAAGTG[C/T]CAAATGTGAGAAATA | 9169 |
rs182941123 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940940 | CTCCCGAGTAGCTGG[A/G]ACTACAGGTGTGTAT | 9169 |
rs182960324 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936097 | GTTTCTTCTAACATT[C/T]ACTTATTACTAAATA | 9169 |
rs182985610 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975600 | CTCTCAGACTTCACT[A/G]GCTTGAAGAGCGTTA | 9169 |
rs183079778 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957105 | TAAAAAATGTATCTG[A/G]CAATACTTTATAAAT | 9169 |
rs183090177 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45975901 | ATCACTGATCACATA[C/T]CACAACAGATATAAT | 9169 |
rs183163352 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936534 | TAATTTAGCTAACTA[C/T]AACAAAAGTATAAAT | 9169 |
rs183245692 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952823 | ATTTTAACAATCTAA[C/T]AGCAATAGTCTCAAA | 9169 |
rs183256534 | snp | A/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956679 | CTTTCATGTTCTCCA[A/T]GATACCAGTTGGGGA | 9169 |
rs183369367 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982408 | ACGTATATTTACATT[A/T]AAAAATCACCTATCG | 9169 |
rs183478231 | snp | A/T | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930769 | ATAGATTTGTATATA[A/T]TTTATGGTAGTAAAT | 9169 |
rs183492248 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971296 | TGATTAAAGTTGGCA[A/T]TACATTCCAAAATAT | 9169 |
rs183561575 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923795 | TCAAGTGATTCTTGA[A/G]CCTCAGCCTCCGAGT | 9169 |
rs183843914 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941251 | TAGACACCTTACTTA[C/T]CGAAAAACGAATTTG | 9169 |
rs184041278 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960666 | TAGTTTATATGTATA[C/T]TATTATTAATTCAAT | 9169 |
rs184088063 | snp | A/G | 0.000263813 | 0.011482 | missense | SCAF11 | GRCh38.p7 | 12:45927197 | GCTGACTCATTCTTA[A/G]GAGATGGTGATTGAG | 9169 |
rs184094552 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949878 | GTACTTAAAGCTACT[C/G]AAGTATAATAGCTGA | 9169 |
rs184107076 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969308 | AGCCTAGTCTGGTTT[A/G]GTTTCAAATTACTAC | 9169 |
rs184115053 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992153 | GAGTCTGCTCACTGT[C/T]TCACACTGTGAGGAT | 9169 |
rs184129551 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983974 | ATTGAGAACACTTTT[A/T]ATTTTCACTAAAAGT | 9169 |
rs184189657 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920503 | GAATCAGTTTATCAT[A/G]GAGAAAACCTACTGT | 9169 |
rs184201977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942871 | GCGTTTGTCTACGAG[A/G]AGATCCCATTGACAA | 9169 |
rs184205544 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962104 | GAGTAATATTCACAC[A/G]GATCAAAAATTTAAG | 9169 |
rs184339370 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979446 | TGCTTCTGAAATTCT[A/T]CCCCGTTCTGTTTAA | 9169 |
rs184362107 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964680 | TCAAAAAAAAAAAAC[A/G]GAAAGGAAAAGCCTT | 9169 |
rs184408582 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939567 | GCTGGGCATGGTGGC[A/G]CATGCCTGTAATCCC | 9169 |
rs184416894 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932938 | GTTAAACAGATAAAT[G/T]AAGGATTCTTTACTT | 9169 |
rs184421065 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959426 | TTAACATAGTGAATT[A/C]AATGAAATTAAATGT | 9169 |
rs184494580 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985940 | CTCTTCTTGACTTCT[A/C/T]TCTCCTTGTAACATT | 9169 |
rs184658946 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938027 | GGTATGTGTACTGTC[C/T]TGAGATTCTTAACTC | 9169 |
rs184671145 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977761 | CTGCCACAAGATGAG[C/T]TTGGGAGGGGGTGTT | 9169 |
rs184809332 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958540 | AAATTTCAGCCTTCC[C/T]TAATGTCAATTATTG | 9169 |
rs184814461 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953711 | CGTAAAAACTAAGAT[G/T]TATAGAGGCCATGAA | 9169 |
rs184825842 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972123 | GAAATATAAGATAAA[C/T]CTCCACACATGTCAC | 9169 |
rs184913092 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930986 | TGTTCAAGGGTCAAC[C/T]GTATTATTATAGTCA | 9169 |
rs184942821 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955124 | TAATTTAGTTAACAC[C/T]AAAAAATAAGTTAAT | 9169 |
rs185035418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934036 | GTTTACCTTCCCCCC[C/T]GCCCAAAAAAAAACT | 9169 |
rs185058689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974142 | GTAGTCCATGAAGTG[A/T]GCAACAGCATTATGT | 9169 |
rs185066818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949224 | ATAGACTAGATCTAT[A/G]CTGTCCAAGACAACA | 9169 |
rs185111114 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975390 | GCTGGCTCATCTGCA[C/T]TAAAAATCTTTTGTT | 9169 |
rs185238420 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925690 | TAAATTATAAGGTTA[C/T]TCAATTTTTACATCT | 9169 |
rs185357928 | snp | G/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948777 | TGCTTATAACAGAGA[G/T]ATGAACACAGATTTG | 9169 |
rs185374213 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990856 | AGCTGCGCTGGAGGG[A/G]CCTTCTGGGAAACGT | 9169 |
rs185405257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945463 | AATGGTTTAAGGATA[C/T]TCTCACAGACTCCTA | 9169 |
rs185480584 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944266 | ATATCTAAAGCTGAC[A/G]AAAGAAAAATGCCTT | 9169 |
rs185493671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984851 | AGGCATGGGCCACTA[C/T]ACCTGGCTAAATTTT | 9169 |
rs185595034 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921843 | CCCTTGAATTTTGTG[A/G]GGGAGGGTGGAGGGG | 9169 |
rs185618895 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963618 | AAAATAAATGAAGAG[A/G]AAATAAACTCAAGCA | 9169 |
rs185720609 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991131 | ACCTGAAATGCAGCC[C/T]GTGGAGTGAAGAGTC | 9169 |
rs185848732 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968669 | AGTGACGCAGGGCAC[A/G]GTGGCTCACACCTGT | 9169 |
rs185871144 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923746 | GGAGTGCAGTGGCGC[C/G]ATCTTGGCTCACTGC | 9169 |
rs185873208 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945883 | TTTTACTAGACACGA[C/G]GTCTCACTATGTTGC | 9169 |
rs185881352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965262 | TAAGCAGAGATATTT[C/G]CATAGCTAAAGTAAC | 9169 |
rs185890452 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986842 | CTTGCCACCAACCAC[C/T]ATGTAAGAAGTGCCC | 9169 |
rs185972221 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935805 | TATTTCTGGGTAATT[C/G]TCAGGTAATTACTCA | 9169 |
rs186103716 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956259 | AATACCTATGTTTAT[A/G]GGTAGGTTTGCCTGT | 9169 |
rs186111397 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974899 | CTGTAGCCTTATGAA[A/G]TGTATTTCTAACAGA | 9169 |
rs186124120 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941046 | TCATTAGTCTTAAAC[A/G]TTCTGCCTGAACTCA | 9169 |
rs186124193 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960455 | ACCATGTGCACTAAA[C/T]TCAACACAGATAAAA | 9169 |
rs186134877 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982149 | CAATGAAGCTATTTC[A/C/G]TTTCATCCATCTCCC | 9169 |
rs186194634 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935177 | CCTATTGACATTGTT[C/G]AAAATAAATCACACT | 9169 |
rs186198626 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955596 | GGTTTTAAAAGTTCA[C/T]ATTTTAAACTAATGT | 9169 |
rs186218101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980714 | ATCTGAGTCCAGTGG[C/T]AATAAATAGCAGCTA | 9169 |
rs186355188 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960270 | ATTACATACACATTA[C/T]AATTTTCTTAGAGCA | 9169 |
rs186441004 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980001 | AACCTAGATTTTTGT[A/G]TAAGCGTTTCATATT | 9169 |
rs186444240 | snp | C/T | 0.00195899 | 0.0312355 | missense | SCAF11 | GRCh38.p7 | 12:45928785 | TTGATCCTCTGGTAT[C/T]TGATGTACCAGAAGT | 9169 |
rs186446140 | snp | A/C | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951180 | TTGTTTTTCAGGAAA[A/C]CACAGTTTTCAGTTA | 9169 |
rs186452866 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970310 | ATGCCGGGATTACAA[A/G]CATGTGCCACTGTGC | 9169 |
rs186474704 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956810 | TTCTGACATTTAAAA[C/G]TAGGCACAAAGAAAT | 9169 |
rs186675636 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975618 | TTGAAGAGCGTTAGA[A/G]ACGCGCTCTGGATTA | 9169 |
rs186679618 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923995 | AGCTGGGATTACAGG[C/T]GCTTGCCACCACACC | 9169 |
rs186690864 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948061 | ATAAACTGAAAAGAA[C/G]GAATTCTTTTAATTC | 9169 |
rs186691943 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967113 | TATTTTAAAGTGGGG[G/T]GCATTGGTATATGCC | 9169 |
rs186761500 | snp | A/G | 6.59304e-05 | 0.00574116 | missense | SCAF11 | GRCh38.p7 | 12:45928073 | TTTGGAAGATGAACT[A/G]TACATACATCTGTCT | 9169 |
rs186766371 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936291 | GGACTACAGGCGCAC[A/C]CCACCACGCCCGGCT | 9169 |
rs186776754 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969584 | TCATTATTATTCTTA[C/T]TGTCAGAAACAACAG | 9169 |
rs186892172 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951973 | TAAGATATGCTGCCC[A/G]GTTGAGAACTACTAG | 9169 |
rs186896726 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970976 | AATTATTGAAACAAA[A/T]CATTTTCTAAAGAGT | 9169 |
rs186898479 | snp | A/G | 0.00438332 | 0.0466095 | utr-variant-3-prime | SCAF11 | GRCh38.p7 | 12:45919272 | TCACTGTGCTTCTGA[A/G]GCTACATCTTTTGGA | 9169 |
rs186899717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942442 | TTCTTCCCTTCACAG[C/T]CAGAGTAATCCTTTT | 9169 |
rs186911791 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961591 | GAAATTTGTCCAAAG[C/T]AGGAAGAAAATACAT | 9169 |
rs186976079 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950825 | CCATCCCCTTTTCTA[C/T]TTACATAGACAGTAA | 9169 |
rs186998151 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993364 | GGTAATCAACGTATT[G/T]ATTTTGATGGAGCTT | 9169 |
rs187044756 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947596 | CAGTGCTATTTACAG[C/T]GTGGTATGAGCACCA | 9169 |
rs187063498 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988085 | TACTGCTCAGAAGCA[A/C]GACAAGGTGCAAGGT | 9169 |
rs187114000 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948328 | GTGTGTGCTTTTGAA[A/T]AAGTGATTAAATACA | 9169 |
rs187139806 | snp | A/T | 0.0111196 | 0.0737302 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967657 | TCAAAAAGAAAGAAA[A/T]CTGCTTTAAAAACTG | 9169 |
rs187148145 | snp | A/G | 0.00953873 | 0.0683987 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990517 | GGTCCGGAGGCGGCG[A/G]CGAAGCAGGGAGCGA | 9169 |
rs187243977 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965771 | TCTATTAATTTCTAA[A/T]ATAATTTACACATGG | 9169 |
rs187333276 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923856 | CTGGCTAATTTTTGT[A/C]TTTTTTTTTTTCTAG | 9169 |
rs187352603 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984412 | GATGTGTTTTTCTCA[C/T]TGTGTCCTGTCAAAT | 9169 |
rs187399518 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959670 | ATGCTTTGAAACATA[C/T]CTATTTTTATCACAG | 9169 |
rs187558653 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937292 | TTGTATTTTTGCTGT[A/G]ATATTTTTAACTTCT | 9169 |
rs187571526 | snp | A/T | 0.00993419 | 0.0697739 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977019 | AAAAGCCTTCCAAAA[A/T]AGAAACCTCGAGGCC | 9169 |
rs187648065 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939935 | CCCCCACTAACTCTA[C/T]CTTCGTGACTTTGTC | 9169 |
rs187762736 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936666 | CTCTCAAAGCTGCTG[C/T]TCAATAGTCATTTTG | 9169 |
rs187781034 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957125 | ACTTTATAAATTATA[A/G]ATGACTAATGTTAGT | 9169 |
rs187788785 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982985 | GCCAAATGTGAGAAA[A/T]AGGCAAAGAGTTTCT | 9169 |
rs187789177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976644 | GAAGTTACAGAGGAA[C/G]AAAAACAGAGGGAAC | 9169 |
rs187821358 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989231 | TGATATGTAGAAATT[A/T]ATTTTTCTTTTAAAA | 9169 |
rs187825569 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957850 | TATTTTAAGGGCCAA[A/T]TTTTTAATCACTTCT | 9169 |
rs188014765 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931440 | CATCAAACACACATT[A/T]TTATGAAACTGGAAG | 9169 |
rs188031854 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972411 | ACAAAGTGAGATCCT[C/T]TCTCTACAAAAAATA | 9169 |
rs188088262 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924603 | GATTATGAAGGTTTA[A/C]CATAACTGAAATCAA | 9169 |
rs188119879 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930101 | CATTATAATGCTGTA[A/C]TGTATTTATTGATAC | 9169 |
rs188266920 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949248 | GACAACAGTCACTAG[A/C]CACATATGGCCACTC | 9169 |
rs188272934 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968802 | AAAAAATTAGCCGGG[A/C]GTGGTGTAATCCCAG | 9169 |
rs188282888 | snp | C/T | 0.00639516 | 0.0561844 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991849 | CCTGCTTGCGGCTCC[C/T]GCAGGACTAAGCTCT | 9169 |
rs188333960 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971944 | GAAAACCAATTTTCT[A/G]GCCAAAAGACAGAAA | 9169 |
rs188414743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930808 | AGACTAGTACCTACA[C/T]ATATTTTATACATTA | 9169 |
rs188494768 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923245 | ACATTAAAAAACACA[A/G]AGCAAACCAACCTTA | 9169 |
rs188509311 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945529 | TATTGAGTTGTATTA[C/T]CTCAGTCTTTTTTTT | 9169 |
rs188517139 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965028 | CCATGAATTTTATCT[A/G]AAAAATCACAGTGAG | 9169 |
rs188521241 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986528 | CCTCCCTTTCAATAC[A/C]CATCACCACAATCCT | 9169 |
rs188591777 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990910 | ACACTGCGGATGGTG[C/T]GCATGCGCAGCGCGT | 9169 |
rs188614764 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952829 | ACAATCTAATAGCAA[C/T]AGTCTCAAAGAGCAA | 9169 |
rs188671407 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948788 | GAGATATGAACACAG[A/G]TTTGTATATACATAT | 9169 |
rs188677883 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938255 | AGCACTCTGGGAGGC[C/T]GAGGTTGGCGGATCA | 9169 |
rs188743666 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969430 | TCCCTCTCCCTCCTT[A/G]CTCTTGCTGTTCTCT | 9169 |
rs188751909 | snp | A/C | 0.000798403 | 0.0199641 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993178 | AGTTGATATATGAAC[A/C]ATCATTGTCAACATT | 9169 |
rs188866196 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968638 | GCCAGCCACTACACT[A/G]CATTCAAATAATGGT | 9169 |
rs188894117 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961119 | TTCAGACTCTGAAAT[G/T]AGTCCACACTAAATT | 9169 |
rs188901076 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921135 | TTACAGGCGCCCACC[A/G]CCACGCCTGGCTAAT | 9169 |
rs188903207 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943101 | CTGCTTCATCCAATA[A/C]ATAATCTATTTCAAT | 9169 |
rs188911011 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963167 | GTCTAACATACTAAT[A/T]GAAATCCAAAAGAGA | 9169 |
rs188947977 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926043 | TTCAGCTTATTATAA[A/G]AACTACAAATAAGGA | 9169 |
rs189084081 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980006 | AGATTTTTGTGTAAG[C/T]GTTTCATATTATTTT | 9169 |
rs189150082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939858 | TTAAATTATCCTTAG[A/G]CTATATCATGGTTTC | 9169 |
rs189151803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959481 | ATAAGGCATGGCCTG[C/T]TAGAAGGCTGAAGAC | 9169 |
rs189157101 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941357 | GTACACATTGTGAAA[A/T]TAATCACCACAAACC | 9169 |
rs189160830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940195 | TAAAGGCAAAAACTC[C/T]TAAAGGTTCTAATCT | 9169 |
rs189162032 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979931 | CATAAGGCATGAATA[C/G]ATATTGGGATTCTTT | 9169 |
rs189178636 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982504 | TTGAGGTCAGGAGTT[C/T]GAGATCAGCCTGACC | 9169 |
rs189362775 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959687 | TATTTTTATCACAGC[A/T]ATAAAAGATTCAAAC | 9169 |
rs189379913 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954944 | GATTCCCCCCCTTTT[A/T]TTTCCTTAAGCATAA | 9169 |
rs189395158 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955915 | AGTGTAATGTGTATT[A/C]AACAGAGCATATGTT | 9169 |
rs189403341 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975009 | ATCTCCGTGTATTTC[C/T]ATCAGAGTTCTTGGA | 9169 |
rs189627631 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929206 | GCTGGAGTGCAATGG[C/T]GTGATCACTGGAGCA | 9169 |
rs189631811 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951381 | GCCTTAGTACAAAAC[A/G]TCCTTCAGATTATCA | 9169 |
rs189643992 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970523 | GTGAATAAAAGGGAA[A/C]GTAGAAGCAGTCTCT | 9169 |
rs189659962 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932961 | CTTTACTTTCTAAGG[A/G]GTCCTTTATATAGCA | 9169 |
rs189732255 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958914 | AAATATACTAGACTA[C/T]GACACACTTTAATTT | 9169 |
rs189736651 | snp | C/T | 3.3e-05 | 0.00406189 | missense | SCAF11 | GRCh38.p7 | 12:45927275 | GGCCGCTTCTTTTCT[C/T]GTGGAGTGTCTTTGT | 9169 |
rs189863493 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924307 | ATAAACAGCTTTATC[C/T]AGTGTTTGTCTGAAC | 9169 |
rs189880074 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948090 | TCTTTTTATTTTGTG[C/T]TATTTTTTAGTAGAG | 9169 |
rs189881781 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967312 | TACATGAGAAACTGA[G/T]AAACCTCAATCAAGT | 9169 |
rs189896273 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989517 | TTTGAATCCGTGAAT[A/G]TCTAAATCAAGTACT | 9169 |
rs189896987 | snp | A/C | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978843 | ATACTTGCAAATAAT[A/C]AAGAAAGCTCTCTTA | 9169 |
rs189903182 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950279 | CAAGAAGTTCAATTG[C/T]AAAGGGAAAAAGATA | 9169 |
rs189985030 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974481 | CTCTCAAACTCTGCC[A/G]CTGTGTTATCAACTA | 9169 |
rs190234599 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955425 | AAAGTGTTGGGATTA[A/C]AAGCGTGAGCCACCA | 9169 |
rs190315424 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940842 | GGGTCTTACTCTGGC[A/G]CCCACGCTGGAGTGC | 9169 |
rs190328429 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960338 | TATGTGGTCACCAAA[C/T]ACAATCTTATAAAAA | 9169 |
rs190438745 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964390 | GGAAAAGCCTTGGCC[A/G]TGCACGGTGGCTCAC | 9169 |
rs190516931 | snp | A/G | 0.00105834 | 0.0229793 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45922543 | ATGGCTTGATGGCCA[A/G]TTTTACCTCTTGTGC | 9169 |
rs190560808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936302 | GCACACCACCACGCC[C/T]GGCTAATTTTGGTAT | 9169 |
rs190562869 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987331 | CTTGGCAGTTTATGC[C/T]ACAGACTGAGACTTG | 9169 |
rs190563784 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956887 | AGATATATGCTTTAG[A/G]TGATGGGTGTTCACA | 9169 |
rs190700414 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985070 | CTGGAATCAACCATT[C/T]CTCCAAAGAGTGGTT | 9169 |
rs190789190 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941197 | TTATTTGTACATGAA[A/C]TGCAAATATACAATT | 9169 |
rs190793128 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960526 | ATTAAACAGTGATCC[C/T]ACACAGAGAGAGATT | 9169 |
rs190806592 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982292 | TTTCAGGTGAGTGAT[A/G]GCTTATAAATTTTTT | 9169 |
rs190950604 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935600 | TTTATGCCCTAAGGA[C/T]GCTGAGTTGTTTTGT | 9169 |
rs191025808 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956401 | AATGCTTATTTTAAA[A/G]CTATTTTCCAGGACC | 9169 |
rs191183706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975569 | TTCAAACTTTTCTTC[C/T]GCAGCTTCCTTATCC | 9169 |
rs191184341 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971168 | TCCTTCTTCATTTAA[C/T]GTAGCATCATCTCCT | 9169 |
rs191265291 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936086 | ATCCTTTGGCTGTTT[C/G]TTCTAACATTTACTT | 9169 |
rs191276222 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930590 | AATAGCAACAGGTGG[C/T]GGCCACAAAAATTGT | 9169 |
rs191286979 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954669 | TGAACTCCTGGGGCT[C/G]AAGCAATTCTTCCAC | 9169 |
rs191373380 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932317 | TTTCTTTTTCTTATT[C/G]ATTTAGGTCTCCTAA | 9169 |
rs191485443 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946382 | CAAGACTCCAAAAAA[G/T]AGTATAATGTAAATA | 9169 |
rs191510588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981095 | ACCAAAATAATGCTG[C/T]TAGAGATTGAGTGAT | 9169 |
rs191516775 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952020 | TTGGGCTGACAGCAG[C/T]AGTTCTGTGATGTAA | 9169 |
rs191520196 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975738 | CTAATTTCAATACTG[C/T]TGAGAAACAGGGAGG | 9169 |
rs191689809 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942474 | AAATGTACCAGATCA[C/T]GTTACTCCTGAAAAC | 9169 |
rs191692429 | snp | A/G | 0.0023933 | 0.0345097 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919470 | GACTAGTAAGTTAAC[A/G]GGACCAAGGTTTCAA | 9169 |
rs191705722 | snp | A/T | 1.78589e-05 | 0.00298817 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961646 | CAGTATCAACTCTTT[A/T]GGTGAAATGAAATCA | 9169 |
rs191710418 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983090 | AGTGCAAAAAGTTAA[C/T]GTTCTTAAGTCCAAT | 9169 |