SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs191744061 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993460 | GGAGGAAATCATGCT[C/G]TAAATATACTGGATT | 9169 |
rs191818957 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951058 | TTTTTTGTTTTTTCA[A/G]GTAAGCAAAAAATTA | 9169 |
rs191848038 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923759 | GCGATCTTGGCTCAC[C/T]GCAATCTCCGACTAC | 9169 |
rs191942097 | snp | C/G | 0.00557542 | 0.0525036 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990757 | CCAGTTGGGCCGCAG[C/G]GGGGCGCTGGCAAAC | 9169 |
rs191953793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958979 | TAAGAATGTGTTCAA[C/T]GCCTAAAATATTAAG | 9169 |
rs191958382 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979093 | TGGGGCTTTTAGGAG[A/G]TGATTAGGCTGTGAG | 9169 |
rs192027980 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923919 | GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT | 9169 |
rs192041915 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966536 | ACAGTGTGGCTATTA[A/C]GGAATAAAAAAAGAG | 9169 |
rs192115019 | snp | A/C/T | 3.298e-05 | 0.00406068 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928252 | CTCACCAACTAGCAC[A/C/T]GGAAGATCTTGAGCA | 9169 |
rs192129691 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969700 | CAACATTACTAAATA[A/T]CAACTAAATTGATCA | 9169 |
rs192184482 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982818 | ACTTCTGTTTTGGTT[G/T]ACTTTAAGCTGCTAA | 9169 |
rs192204766 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963353 | CTTAAAAGCAGAAAA[C/T]TGGAAAAGACAGATC | 9169 |
rs192214163 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984802 | CAGGTTCAAGCGATT[C/T]TTGTGCCTCAGCCTC | 9169 |
rs192255524 | snp | A/C | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941937 | AGACAGCAAGACCAA[A/C]CCCTTCTCTTCCTTA | 9169 |
rs192293087 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988406 | AGATGTTACTGATGA[C/T]GAATCAACAGTATCA | 9169 |
rs192316137 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930970 | CAGTTAAAACCTATG[C/T]TGTTCAAGGGTCAAC | 9169 |
rs192379555 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947830 | TGCAGCCATGTGTCA[A/C]CATGCCCGGCTAATC | 9169 |
rs192513491 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957903 | TTCCTACTTTCTCTC[C/T]TTTTTTTGAGATAGG | 9169 |
rs192522049 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937147 | ATTACTTTTTTAAAA[A/G]TAAATTTTTGCATTT | 9169 |
rs192528437 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957502 | CACCTTAATAAGACA[C/G]TTCATTTCTAGTTTA | 9169 |
rs192530303 | snp | C/T | 3.57827e-05 | 0.00422966 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926111 | ATTCTTCAAATAAAA[C/T]AGTATCAATAAACCA | 9169 |
rs192531741 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976757 | TTCTATCAGAAAAGG[C/T]CTCAAATCAGTAATT | 9169 |
rs192650175 | snp | C/G | 0.00517822 | 0.0506191 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918794 | TTCTCAGTACGTCAA[C/G]TGAAAATGAAAGGTT | 9169 |
rs192666476 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961255 | ATGGAAGGACACTAT[C/G]GTATCTGCTCTGGTT | 9169 |
rs192802284 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937342 | TTATTTTTCTTGTAT[C/T]ATTGATAAAATATCC | 9169 |
rs192814249 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977495 | AAATCTTGACTGTAG[C/T]GGTAATACAGATCTA | 9169 |
rs192877552 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948358 | ATTTAAACCCCACTT[C/T]ATTTTTTTAATACCT | 9169 |
rs192992332 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952878 | GATATATTATTCCTA[A/C/T]GTAAAAAATGTGATC | 9169 |
rs192995015 | snp | C/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921666 | TTTACATTTTAACCT[C/G]ACAGAATAAATGCAT | 9169 |
rs193038413 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968133 | TCATGTTATATTCTA[C/T]CTATACTACTTATTA | 9169 |
rs193075620 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925323 | TTTGGGAGGCCAAGG[C/T]GGGCAGATCACCTGA | 9169 |
rs193106075 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968642 | GCCACTACACTGCAT[C/T]CAAATAATGGTAGTG | 9169 |
rs193200766 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972097 | GCAGCATACCACCGA[C/T]TCTGAAAACTGAAAT | 9169 |
rs193201150 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943105 | TTCATCCAATAAATA[A/T]TCTATTTCAATATAG | 9169 |
rs193258680 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949155 | CCAGTTAAGGAGAGA[C/T]TATAAAAACCAGGCT | 9169 |
rs193264249 | snp | C/G | 0.00358779 | 0.0422022 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990970 | TTTTACAGGCTGCGT[C/G]GCGGAGGACAATGAA | 9169 |
rs199516827 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984152 | TCTTTTTACCTTAAT[-/A]AAAAAGAAAAAGGGA | 9169 |
rs199574982 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972892 | TATAGATATATATAT[A/C]GATATATATATATAT | 9169 |
rs199581239 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968036 | GGTAAGATGTGGGTA[C/G]GTAGGACTACCCTTC | 9169 |
rs199589025 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964247 | CCAATAATATCAATT[-/A]AAAAAAAATCCTAAA | 9169 |
rs199609774 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985121 | TTTAGAAAACAAGAT[C/T]TGGATGCTCTAATTA | 9169 |
rs199654082 | snp | A/C/T | 3.29675e-05 | 0.00405991 | missense | SCAF11 | GRCh38.p7 | 12:45928314 | CCTCTGTATCATAAT[A/C/T]TGCAGTATGCTTCTC | 9169 |
rs199659318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982618 | ACTGAGGCAGGAGAA[C/T]TGCTTGAACTTGGGA | 9169 |
rs199665541 | in-del | -/ATATATATATATATAGATATATATATAGAT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972866 | TATATATATATATCG[lengthTooLong]ATATATATATATAGA | 9169 |
rs199686825 | snp | A/G | 0.000595152 | 0.0172401 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923198 | GAATTACTTGTACTC[A/G]ATAGAAGTCTTTTAG | 9169 |
rs199712406 | in-del | -/A | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930000 | ACAGTGAATTAATAT[-/A]TTTTTTATGTTATGT | 9169 |
rs199797157 | snp | C/G | 0.000132884 | 0.00815011 | missense | SCAF11 | GRCh38.p7 | 12:45951724 | TAGGACATGAAGCCA[C/G]TGTCTGAAAAGTGAT | 9169 |
rs199820146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937877 | GTCTTTCATTGGGTA[C/T]TCCCCTTCCTCTACC | 9169 |
rs199825706 | snp | A/G | 4.98244e-05 | 0.00499096 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927706 | ATTTTTTAGTAAGTT[A/G]TTTTCAGAGTCTTGA | 9169 |
rs199849899 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988249 | AAGTTACAATGAAAA[A/T]TATTCTACAGTTGAC | 9169 |
rs199864732 | snp | C/T | 4.94336e-05 | 0.00497135 | missense | SCAF11 | GRCh38.p7 | 12:45924867 | ACTCCTGTGTGGAGA[C/T]GCAAGGGTAGCTGAG | 9169 |
rs199882318 | snp | C/T | 0.000378803 | 0.0137571 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45923038 | GCTGTGACTTGATGA[C/T]GAAGTATTACCAGAA | 9169 |
rs199885089 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946019 | TAAACAACAATCTTA[C/T]TGGCTGATCATGACT | 9169 |
rs199957427 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926127 | AGTATCAATAAACCA[A/G]CAAGAATACATTACC | 9169 |
rs199995851 | snp | G/T | 6.62339e-05 | 0.00575435 | missense | SCAF11 | GRCh38.p7 | 12:45927658 | TTCATTCTTTTCTTC[G/T]AAAGATTTTTCCAAT | 9169 |
rs200034095 | snp | A/G | 5.00446e-05 | 0.00500198 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922038 | AATGTCCTTGACAGC[A/G]TTCCCCATTTCAGCC | 9169 |
rs200035348 | snp | A/G | 9.92983e-05 | 0.00704552 | missense | SCAF11 | GRCh38.p7 | 12:45927797 | GTTTCAACATGCCCA[A/G]GCAATTGAACCTCTG | 9169 |
rs200054395 | snp | C/T | 3.43536e-05 | 0.00414435 | missense | SCAF11 | GRCh38.p7 | 12:45931590 | GGACTTCTGTTTCAA[C/T]ATTCCAGGGTATAAA | 9169 |
rs200065536 | in-del | -/AC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986618 | CAATAAGATAGTTAT[-/AC]TGCTTGATATGGTTT | 9169 |
rs200066473 | snp | A/G | 0.00199792 | 0.0315431 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926241 | GTACATCTGCTGGCA[A/G]AGTCTTTCTCACGGC | 9169 |
rs200069087 | in-del | -/AT | 0.443866 | 0.157848 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972866 | TATATATATATATCG[-/AT]ATATATATATATAGA | 9169 |
rs200096019 | snp | A/G | 1.65304e-05 | 0.00287488 | missense | SCAF11 | GRCh38.p7 | 12:45927987 | ACTCTACATTCTCAG[A/G]TAAGTCACTTAGGGG | 9169 |
rs200168517 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951618 | TTCAATTAATTTTTA[C/T]ATAATTCATGTTGCA | 9169 |
rs200172874 | snp | A/G | 6.59131e-05 | 0.0057404 | missense | SCAF11 | GRCh38.p7 | 12:45926876 | GTTCTACATCTTGAG[A/G]GGGACCTAGAATGAG | 9169 |
rs200226879 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982130 | TTCTGTGGCAGTTTT[A/C]AAACAATGAAGCTAT | 9169 |
rs200271295 | snp | G/T | 0.000399281 | 0.0141238 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923042 | TGACTTGATGACGAA[G/T]TATTACCAGAACTTG | 9169 |
rs200390667 | snp | A/G | 0.000810983 | 0.0201205 | missense | SCAF11 | GRCh38.p7 | 12:45927764 | GTATCACATGTTGCA[A/G]TTATTTCTACATCTT | 9169 |
rs200486339 | snp | A/G/T | 0.000774657 | 0.0196656 | synonymous-codon, missense | SCAF11 | GRCh38.p7 | 12:45927174 | AACGGGATTTTTTCC[A/G/T]GCCTCTGGCTGACTC | 9169 |
rs200576932 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984158 | TTACCTTAATAAAAA[-/G]AAAAAGGGATTACTT | 9169 |
rs200634364 | in-del | -/AG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955183 | ATTTTTTTTTTAAAC[-/AG]GGTCTCACCCTCTTG | 9169 |
rs200672317 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972953 | AGATATATATATAGA[G/T]ATATAGATATATATA | 9169 |
rs200691448 | snp | C/T | 0.00313746 | 0.0394827 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924737 | ACATACCTGCAATTG[C/T]TTTCCATCTGGTTGT | 9169 |
rs200780296 | snp | C/T | 6.63504e-05 | 0.00575941 | missense | SCAF11 | GRCh38.p7 | 12:45927872 | TCAGAAGATTCTAAC[C/T]TGGGGCTCTCTATAA | 9169 |
rs200795073 | snp | A/T | 0.0649335 | 0.168079 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928872 | TACCTAATAATATTT[A/T]AAAAAAAAAAAAAAG | 9169 |
rs200803079 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922446 | CGTGCACATACTCCA[C/T]TAAAGCCATAACTTA | 9169 |
rs201003016 | snp | A/T | 0.00135033 | 0.0259488 | missense | SCAF11 | GRCh38.p7 | 12:45927416 | ACCTTTTCATCCGCA[A/T]GATCAGAAGACGGCA | 9169 |
rs201037196 | in-del | -/TGC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945225 | AAAAAAAAGGTAGAA[-/TGC]TCCACAAGCAAAAAG | 9169 |
rs201110082 | in-del | -/A | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918714 | CCATCTCAAAAAAAG[-/A]AAAAAAAAAGAGAAT | 9169 |
rs201111961 | snp | A/G | 2.0304e-05 | 0.00318615 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948564 | GCAAAATCAATTTAG[A/G]GCAACAATCCAGCCT | 9169 |
rs201119358 | snp | C/T | 0.00182427 | 0.0301464 | missense | SCAF11 | GRCh38.p7 | 12:45951664 | CCTTAACATAACCTT[C/T]CAATGCACTGAATTT | 9169 |
rs201143721 | snp | A/T | 0.00420645 | 0.0456676 | utr-variant-5-prime, missense | SCAF11 | GRCh38.p7 | 12:45964181 | ATTTCTCTTTGGAAA[A/T]GGGTTTCCTATAAGA | 9169 |
rs201149754 | in-del | -/T | 0.0383715 | 0.133092 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959254 | GCCTGGGTGACAGAC[-/T]GAGACTCTGTCTCAA | 9169 |
rs201178683 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943079 | AAATGTAATATCTAA[A/G]TATAAGCTGCTTCAT | 9169 |
rs201224550 | snp | G/T | 9.88517e-05 | 0.00702966 | missense | SCAF11 | GRCh38.p7 | 12:45928761 | GAGTTGTCATTGCAG[G/T]TTTTCGTCTTGATCC | 9169 |
rs201238940 | snp | A/G | 0.000197677 | 0.0099398 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45922960 | CTTCGAGCTATCTGC[A/G]CTGGCTTCCACTGCA | 9169 |
rs201305916 | snp | A/G | 3.29777e-05 | 0.00406051 | missense | SCAF11 | GRCh38.p7 | 12:45926673 | TGTCAGCAGAATTTG[A/G]ATCATCAGCATCTAG | 9169 |
rs201355293 | snp | C/T | 0.00199802 | 0.0315439 | missense | SCAF11 | GRCh38.p7 | 12:45927743 | TTGAAATCTTCATTC[C/T]CAAAAGTATCACATG | 9169 |
rs201359258 | snp | A/G | 3.29565e-05 | 0.00405921 | missense | SCAF11 | GRCh38.p7 | 12:45927413 | TCAACCTTTTCATCC[A/G]CAAGATCAGAAGACG | 9169 |
rs201370048 | snp | A/G | 0.000261637 | 0.0114346 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925108 | CTTGTGAAAAAAATC[A/G]TGTTATAAATCTCTT | 9169 |
rs201384582 | snp | C/T | 1.67175e-05 | 0.0028911 | missense | SCAF11 | GRCh38.p7 | 12:45933150 | CAATTCCAGGTAATG[C/T]ATCAGGAAACCATGA | 9169 |
rs201459841 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971195 | TCCTTAACAGAAATT[A/G]TACTGTTGCATGCAG | 9169 |
rs201494509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953266 | TTTTTAATAATGCAT[C/T]GTCTAGTTCGAAGAA | 9169 |
rs201520417 | snp | C/T | 0.00199792 | 0.0315431 | missense | SCAF11 | GRCh38.p7 | 12:45926178 | CTTGTTTCATCCATC[C/T]AGACTGTGGACCTGA | 9169 |
rs201675236 | snp | G/T | 0.000646379 | 0.0179659 | missense | SCAF11 | GRCh38.p7 | 12:45931530 | CGAAAGATATGGTAC[G/T]TGTTGGAAAAATAGT | 9169 |
rs201718690 | snp | C/T | 3.29565e-05 | 0.00405921 | missense | SCAF11 | GRCh38.p7 | 12:45928779 | TTCGTCTTGATCCTC[C/T]GGTATTTGATGTACC | 9169 |
rs201739311 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987926 | ATGTATTGAATTTTT[A/G]TGTGTCTATGTACTA | 9169 |
rs201741705 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971716 | TGCTCCTTTTTTTTT[-/T]GTTTTCCCCCTTTCT | 9169 |
rs201762697 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941006 | GGTGGGTTTCGCCAC[A/G]TTGCCTCAATCTTAT | 9169 |
rs201877264 | snp | C/T | 0.000988484 | 0.0222096 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926686 | TGGATCATCAGCATC[C/T]AGATGGATGTCATTT | 9169 |
rs201926084 | snp | C/T | 0.000399281 | 0.0141238 | missense | SCAF11 | GRCh38.p7 | 12:45928023 | ATACAGGTTGGTACA[C/T]TTTGCTTTCAGATGT | 9169 |
rs201926722 | in-del | -/TT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986612 | TTTAACAATAAGATA[-/TT]GTTATACTGCTTGAT | 9169 |
rs201987820 | snp | C/T | 0.00199792 | 0.0315431 | missense | SCAF11 | GRCh38.p7 | 12:45926595 | TTTCTGGATTTCTGG[C/T]TCTTGGATCAGGCCC | 9169 |
rs202016358 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978332 | TTTACTGAAGTACAA[C/T]GACATAACTAATTTA | 9169 |
rs202041881 | snp | A/C | 0.00199792 | 0.0315431 | missense | SCAF11 | GRCh38.p7 | 12:45927972 | CTTCATTAACCACTG[A/C]CTCTACATTCTCAGA | 9169 |
rs202074705 | snp | G/T | 0.00233623 | 0.0340978 | missense | SCAF11 | GRCh38.p7 | 12:45951678 | TCCAATGCACTGAAT[G/T]TAAACACTGCCTGAA | 9169 |
rs202135977 | snp | A/G | 0.000395276 | 0.0140528 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923075 | CCCTGAACCATTCCC[A/G]TATTTCCTGGGGCTG | 9169 |
rs202244513 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934040 | CCTTCCCCCCCGCCC[-/A]AAAAAAAAACTAAAG | 9169 |
rs267603470 | snp | A/G | | | stop-gained | SCAF11 | GRCh38.p7 | 12:45924736 | AACATACCTGCAATT[A/G]CTTTCCATCTGGTTG | 9169 |
rs367566413 | snp | A/G | 3.56398e-05 | 0.00422121 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926115 | TTCAAATAAAACAGT[A/G]TCAATAAACCAACAA | 9169 |
rs367743841 | snp | C/T | 0.000199078 | 0.00997493 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961813 | ATCTGTCAGCCTCAC[C/T]GTACAACAGACCAGT | 9169 |
rs367757829 | snp | A/G | 0.000115364 | 0.00759399 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922416 | ATTTATTAAAACAGA[A/G]GTGGTTCAAAACAAC | 9169 |
rs367783034 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45934278 | GTACTCCAATTTGAT[C/T]TCTGAGGCTAGAAAA | 9169 |
rs367787539 | snp | A/G | 0.000214237 | 0.0103476 | missense | SCAF11 | GRCh38.p7 | 12:45926889 | AGGGGGACCTAGAAT[A/G]AGATCTGGACCTAGA | 9169 |
rs367787548 | snp | C/G | 4.94434e-05 | 0.00497184 | missense | SCAF11 | GRCh38.p7 | 12:45928355 | ATTTGCTCATTGCAA[C/G]TTTTCAAGCAATTAG | 9169 |
rs367797182 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952658 | GAGTTTCTCTGATAA[A/T]ACTACTAAATATTTG | 9169 |
rs367816025 | snp | A/T | 0.0170251 | 0.090679 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981618 | ATTAACTCTAGACTG[A/T]TCACCTATCTCTAAC | 9169 |
rs367816189 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936394 | TGATCCACCCACTTC[A/G]GCCTCCCAAAGTGCT | 9169 |
rs367847152 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930768 | CATAGATTTGTATAT[A/G]TTTTATGGTAGTAAA | 9169 |
rs367857122 | snp | C/T | 0.000141039 | 0.0083964 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948401 | TTAACTTCTGTTCCA[C/T]TCATTTGCATTCCAC | 9169 |
rs367857855 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955329 | CCCAGCTAATTTTTT[-/T]GTAGAGATCGGGTTT | 9169 |
rs367866975 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971910 | GGATCCAGACACAGT[A/T]ACAGAAAATGGAGTA | 9169 |
rs367896028 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930445 | TTTGCGTTGTGTTTT[G/T]TTTTTTTTTTGTTTT | 9169 |
rs367932981 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950613 | TATTACACTTCTATA[A/C]TGTTTTATCTTTTTT | 9169 |
rs367944298 | in-del | -/T | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986087 | GTTCCATCCTAGGCC[-/T]TTTTTCCCCCAAGTT | 9169 |
rs367988696 | snp | C/G | 1.64798e-05 | 0.00287047 | missense | SCAF11 | GRCh38.p7 | 12:45927537 | CACTGCAAAATGAAT[C/G]ACACTCCATAGGTAT | 9169 |
rs368024919 | snp | G/T | 0.000153988 | 0.00877328 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924797 | TGGGGGAGGGGGTGG[G/T]GGTGGTGGTAGTCCC | 9169 |
rs368205920 | in-del | -/C | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937801 | CTGTTGTTTCCTGTA[-/C]CATCATTTATGCTAA | 9169 |
rs368325648 | snp | A/G | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927925 | ATCTTTATGTTCAGT[A/G]ATTTCTACTAGGGAA | 9169 |
rs368420758 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973160 | AACAAAAAGTGAAAA[C/T]GGAAATAAAAATACA | 9169 |
rs368432553 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945516 | AGGTTTTAATATCTA[C/T]TGAGTTGTATTATCT | 9169 |
rs368434787 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988611 | AAAATTATCCGTAAA[A/G]TTTTCTCCATGACAT | 9169 |
rs368451971 | snp | C/G | 1.64874e-05 | 0.00287113 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927172 | AGAACGGGATTTTTT[C/G]CGGCCTCTGGCTGAC | 9169 |
rs368514411 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951380 | AGCCTTAGTACAAAA[C/T]GTCCTTCAGATTATC | 9169 |
rs368535232 | in-del | -/GTTTC | 0.00755907 | 0.0610114 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992797 | GATAATAACAGTATA[-/GTTTC]ATCAAAACTAAAAAT | 9169 |
rs368548369 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957810 | CTCTTAAATGCTTTA[A/C]ACATGTGTCTTCAAA | 9169 |
rs368590646 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929437 | TGCTGGGAATACAGG[C/T]GTGAGCTACTGTGCC | 9169 |
rs368624792 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937787 | CTTAATTTCCCTCTC[C/T]GTTGTTTCCTGTACC | 9169 |
rs368626096 | snp | C/G | 0.000153988 | 0.00877328 | missense | SCAF11 | GRCh38.p7 | 12:45927009 | GGGAAGAATCTTTCA[C/G]TCTTGGCTGAGATCT | 9169 |
rs368692229 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981140 | CTAAATGTAATCTTA[A/T]TATAAATGCTACAAA | 9169 |
rs368695125 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921167 | TTTGTATTTTTAGTA[C/G]AGACGGGATTTCACC | 9169 |
rs368716275 | snp | A/C | 3.29576e-05 | 0.00405928 | missense | SCAF11 | GRCh38.p7 | 12:45927572 | TCATTGTTGTCCTCA[A/C]TAAAATGCTTCTGAA | 9169 |
rs368831751 | snp | A/G | 5.24453e-05 | 0.00512053 | missense | SCAF11 | GRCh38.p7 | 12:45948509 | TTTTTCTTGTCTTTT[A/G]TTTCTCTCAGCTGTT | 9169 |
rs368845787 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951585 | ATATACACAAACTGG[-/A]AATCAAAGTCAAACA | 9169 |
rs368853671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984638 | TTATCTCAGCTTTGG[C/T]TAGTGAAAGCCTTTC | 9169 |
rs368864555 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955426 | AAGTGTTGGGATTAC[A/G]AGCGTGAGCCACCAC | 9169 |
rs369011210 | snp | A/G | 0.000212233 | 0.0102991 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934304 | GAAAAGTAAAAAGTA[A/G]TTAGTGAAACAGCAA | 9169 |
rs369020219 | snp | A/T | | | missense | SCAF11 | GRCh38.p7 | 12:45927092 | CTTTCCCTAGTAGTA[A/T]CCCTTTTTGGAGACC | 9169 |
rs369063294 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938222 | TGGCCAGGCACAGTG[A/G]CTCACAACTGTAATC | 9169 |
rs369193001 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960787 | TTAAGCAAAACATAG[C/T]GCTTTGAAAACCCCA | 9169 |
rs369201119 | snp | A/G | 0.0271762 | 0.113356 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990565 | CGCGCGGCTTAAGCC[A/G]CCGCTACTCCCCCTT | 9169 |
rs369231473 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983115 | TCCAATTAGGACTTA[C/G]GTTGTGTTTCCTTAG | 9169 |
rs369243017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924335 | AACAAGACAATAAAA[C/G]CTTCATCACAGTACT | 9169 |
rs369249749 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954371 | CCTCCTGAGTAGCTG[A/G]GACTACAGGTGCATG | 9169 |
rs369258102 | snp | C/T | 0.000153988 | 0.00877328 | missense | SCAF11 | GRCh38.p7 | 12:45927791 | TCTTCAGTTTCAACA[C/T]GCCCAAGCAATTGAA | 9169 |
rs369277203 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947170 | GAATCTGACAACATA[C/T]TGACTTAAAAATTCA | 9169 |
rs369281583 | snp | A/G | 0.000115349 | 0.00759349 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922432 | GTGGTTCAAAACAAC[A/G]TGCACATACTCCACT | 9169 |
rs369300770 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973886 | TAGGAATGATGGAAG[A/G]TCAACAGAAACAGTA | 9169 |
rs369315183 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968419 | ATAACATATTGTTTC[C/T]GCTAGATACTGAAAG | 9169 |
rs369323018 | in-del | -/CT | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992587 | AATCTCTAGGATTCA[-/CT]CTAGAGAGTGTAACT | 9169 |
rs369338243 | snp | A/C | 0.000400582 | 0.0141467 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933252 | AAGATAAATTTTAGA[A/C]CTTCATCAGAATCTC | 9169 |
rs369403955 | in-del | -/GTTTTAT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977782 | AGGGGGTGTTTGAAT[-/GTTTTAT]CTCTGCTTTCTCCAT | 9169 |
rs369424683 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934064 | ACTAAAGCAAAACAA[C/T]CAGGTGGGCCTTTCA | 9169 |
rs369428457 | in-del | -/A/AA | 0.0253068 | 0.109676 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928871 | TACCTAATAATATTT[-/A/AA]AAAAAAAAAAAAAAA | 9169 |
rs369431160 | snp | A/C | 4.99555e-05 | 0.00499752 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951636 | AATTCATGTTGCAGA[A/C]TAAAAAGACTTACCT | 9169 |
rs369440355 | snp | A/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974527 | TTAACAATGTTCACA[A/T]CTTCAGCAAGAGCAC | 9169 |
rs369442079 | snp | A/C | 1.64803e-05 | 0.00287052 | missense | SCAF11 | GRCh38.p7 | 12:45928537 | AGAGCTCCGAAGTTT[A/C]TTTTTCAGTAAAGGT | 9169 |
rs369471346 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940486 | GTAGAAAGTGGCATT[A/G]GATATAGAGTCAGAA | 9169 |
rs369491261 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975055 | TCAATAAGTAAGTAC[C/T]ATGTTGAAAGGAATC | 9169 |
rs369652954 | snp | C/T | 4.0184e-05 | 0.00448223 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948560 | AAAAGCAAAATCAAT[C/T]TAGAGCAACAATCCA | 9169 |
rs369700732 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932023 | GTACATTTGCTAACT[G/T]TTTACCAAAGTGTGT | 9169 |
rs369763088 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947385 | GGCAATGGTTTTAAC[A/G]GCAACTAAAAAAAAG | 9169 |
rs369813581 | in-del | -/AG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942965 | TGTTAAATGTATGAG[-/AG]TGATCTCAATTCCCT | 9169 |
rs369871644 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954706 | CTCCCAAGTAGCTGG[C/G]ATACATGCATGTATC | 9169 |
rs369933266 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989888 | AAGAAAAGCCGACAC[C/T]GCGGTCGGGAGCGCC | 9169 |
rs369934721 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970300 | GTCTCCTAAAATGCC[A/G]GGATTACAAGCATGT | 9169 |
rs370077453 | snp | C/T | 9.90688e-05 | 0.00703737 | missense | SCAF11 | GRCh38.p7 | 12:45926468 | TAAGTGCCTCTGCCA[C/T]GGTTGCCTCTGCCTC | 9169 |
rs370078181 | snp | C/T | 1.64947e-05 | 0.00287177 | missense | SCAF11 | GRCh38.p7 | 12:45926951 | CTCTGCCCATCTCTA[C/T]CACTTTCTCGTTCTC | 9169 |
rs370116120 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949135 | GGTGTGATATGGGGA[A/C]TCAACCAGTTAAGGA | 9169 |
rs370132161 | in-del | -/AG | 0.499551 | 0.0149693 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972899 | TATATATAGATATAT[-/AG]ATATATATAGATATA | 9169 |
rs370201774 | snp | A/G | 4.99372e-05 | 0.00499661 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961829 | GTACAACAGACCAGT[A/G]GAAATAGTATTATCT | 9169 |
rs370218052 | in-del | -/TCC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972608 | AAAAAAAAAAAAAAA[-/TCC]AAAAAACAAAAACAA | 9169 |
rs370230807 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972883 | ATATATATATATAGA[G/T]ATATATATAGATATA | 9169 |
rs370289169 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969789 | TCGTCCAGGCTGGAG[A/C]GTGGTGGCACAATTA | 9169 |
rs370320281 | snp | C/T | 1.66136e-05 | 0.00288211 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927934 | TTCAGTAATTTCTAC[C/T]AGGGAACTCTCTGTT | 9169 |
rs370387365 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948076 | CGAATTCTTTTAATT[A/C]TTTTTATTTTGTGTT | 9169 |
rs370422923 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919586 | AACATAAATTTCTTA[A/T]CTCAAGAATGAGGAA | 9169 |
rs370468709 | in-del | -/A | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992284 | GTACTGTTTTTGATA[-/A]TGGGGTTTGGGAATT | 9169 |
rs370528229 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926806 | CCATCTTCCCTTCCA[C/T]CGGGGAGAGTAACTA | 9169 |
rs370559362 | snp | A/C/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992472 | TGATTATAAAGGATG[A/C/G]TTGTTAAGAGAAATA | 9169 |
rs370592250 | in-del | -/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980124 | GAAAATAAGTAACAT[-/G]CCCAAGATCGAAAAG | 9169 |
rs370602560 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966967 | TTTAAAAACCTAAGA[A/G]ATGTTCAGATGTAAT | 9169 |
rs370633652 | snp | A/C | 5.00204e-05 | 0.00500077 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945225 | AAAAAAAAAGGTAGA[A/C]TCCACAAGCAAAAAG | 9169 |
rs370637195 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979227 | ACAGCCTAATCACCT[C/T]CTAAAAGCCCCACCA | 9169 |
rs370644814 | snp | A/C | 0.00279162 | 0.0372561 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919998 | CAAAATTGTTTCTAG[A/C]GTTCTAATCTAAAAC | 9169 |
rs370697093 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991151 | AGTGAAGAGTCGGCA[A/G]TTTGGAAGCCCACCT | 9169 |
rs370703577 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979176 | TCTCCAGCCCTTATA[G/T]AAGGCACTAATTCCA | 9169 |
rs370709240 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984926 | CCTTGAACTCCTGAC[C/T]TCAAGTGATCCACCT | 9169 |
rs370719719 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935293 | ACTTAATAGCATACT[A/G]ATTTCCTTTTTAGTT | 9169 |
rs370729762 | snp | C/T | 0.000199967 | 0.00999717 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961726 | TAAGAATACAAGTCA[C/T]ACAGAAGACATGATT | 9169 |
rs370749326 | snp | C/T | 3.54887e-05 | 0.00421225 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961664 | TGAAATGAAATCATG[C/T]TAGGAAATTAAAATA | 9169 |
rs370791718 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964442 | GGAGGCCGAGGCGGG[C/T]GGATCACAAGTTCAG | 9169 |
rs370914168 | snp | C/T | 6.61704e-05 | 0.00575159 | missense | SCAF11 | GRCh38.p7 | 12:45928839 | GAGTATGTGCTAATG[C/T]ATATCCCTTGCAAGA | 9169 |
rs370921146 | snp | C/T | 3.30033e-05 | 0.00406209 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45923131 | ACTCATGTTATTACT[C/T]ACATGAGAAGAACTA | 9169 |
rs371024054 | snp | C/G | 3.50416e-05 | 0.00418564 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934431 | AAGAAAAAGATTTTT[C/G]TTGGTTTCAACAAAC | 9169 |
rs371051019 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962753 | GAAAACTAATCCTGA[C/T]AGACTCCAGTATCAA | 9169 |
rs371070696 | snp | A/C/G | 0.000247341 | 0.0111181 | missense | SCAF11 | GRCh38.p7 | 12:45927134 | TGCCTCCTTTCTCTT[A/C/G]CAATATCCTTTTTTG | 9169 |
rs371117143 | snp | A/G | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918789 | GAAAGTTCTCAGTAC[A/G]TCAAGTGAAAATGAA | 9169 |
rs371213731 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968913 | CCTGGGCGACAGAGC[A/G]AGACTCCATCTTAAA | 9169 |
rs371257166 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973002 | GATATAGATATATAG[-/AT]ATATATATAGATATA | 9169 |
rs371263077 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936369 | CTGGTCTTGAACTCC[G/T]GACCTCAGGTGATCC | 9169 |
rs371265408 | snp | A/T | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963927 | AACAAATCAAAAAAC[A/T]TGATCAGTCGAAAAT | 9169 |
rs371358733 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982834 | ACTTTAAGCTGCTAA[A/G]TAACTACTGTGGTCA | 9169 |
rs371430516 | snp | A/G | 7.0368e-05 | 0.00593119 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948404 | ACTTCTGTTCCACTC[A/G]TTTGCATTCCACTTC | 9169 |
rs371439632 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991487 | GAATCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC | 9169 |
rs371466286 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975592 | CCTTATCCCTCTCAG[A/G]CTTCACTGGCTTGAA | 9169 |
rs371500274 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958046 | GCTGGGACTACAGGC[A/G]TACTCCACCATGCCT | 9169 |
rs371707436 | snp | C/T | 0.00032101 | 0.012665 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931481 | TAATAATTTTTAAAA[C/T]AGAAAATGATTTCAC | 9169 |
rs371731913 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938691 | AATCCGAAAGGATGT[A/T]TCATGAAAACATCCT | 9169 |
rs371735213 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981654 | TTTAAAAAATTAGCC[A/G]AGTGTGGTGGCATGC | 9169 |
rs371753888 | snp | C/T | 1.64833e-05 | 0.00287078 | missense | SCAF11 | GRCh38.p7 | 12:45928440 | CTGGTTGGTGCTCTT[C/T]TTCTAACACAGGTGA | 9169 |
rs371758000 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932146 | GTATCCTTCTCCCTC[C/T]TTTCCAGGCAACCAA | 9169 |
rs371833402 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931049 | CTATCCAGCTGAAAC[A/T]GTATCCTCTGACCAA | 9169 |
rs371876850 | snp | C/T | 0.000153988 | 0.00877328 | missense | SCAF11 | GRCh38.p7 | 12:45927560 | ATAGGTATCATTTCA[C/T]TGTTGTCCTCACTAA | 9169 |
rs371893368 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937341 | ATTATTTTTCTTGTA[C/T]CATTGATAAAATATC | 9169 |
rs371897313 | snp | A/C/G | 4.942e-05 | 0.00497071 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926254 | CAAAGTCTTTCTCAC[A/C/G]GCCCAGCTGGATGCA | 9169 |
rs371989659 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923801 | GATTCTTGAGCCTCA[A/G]CCTCCGAGTAGCTGG | 9169 |
rs372020007 | in-del | -/CTC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986860 | GTAAGAAGTGCCCTT[-/CTC]CTCCCACCAAGATTC | 9169 |
rs372053899 | in-del | -/GGG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989954 | GAGGGTGTCTGTGGC[-/GGG]GGTTCTGGCGTGGAG | 9169 |
rs372088219 | snp | A/G | 0.000197981 | 0.00994742 | missense | SCAF11 | GRCh38.p7 | 12:45927038 | CTTTTGTTCTCTCTA[A/G]AAGTTTCTCTTCTTG | 9169 |
rs372113921 | snp | C/T | 4.94442e-05 | 0.00497188 | missense | SCAF11 | GRCh38.p7 | 12:45928349 | TCTTCTATTTGCTCA[C/T]TGCAACTTTTCAAGC | 9169 |
rs372155382 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45974066 | AGTAATAAAACAATA[A/T]TGCAATAAAGCAAGT | 9169 |
rs372170014 | snp | C/T | 0.0271762 | 0.113356 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974649 | TCTTCAGGCTCCACT[C/T]CTAATTCTATAATAG | 9169 |
rs372198329 | in-del | -/C | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989976 | GGCGTGGAGCCCCTT[-/C]CCCCCCCCCCGTAGG | 9169 |
rs372233487 | snp | C/T | 2.05818e-05 | 0.00320788 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948566 | AAAATCAATTTAGAG[C/T]AACAATCCAGCCTTA | 9169 |
rs372237536 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983475 | CAAAATACCAGAACA[C/T]GATACATTTAAAAAA | 9169 |
rs372260883 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934746 | GTGAAGTATGTCAAA[C/T]CTGCTATGTTTACAA | 9169 |
rs372267690 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971246 | AAAAAATTATAAAAT[A/G]TAATTCTCAAACTGT | 9169 |
rs372270232 | snp | A/G | 0.000283914 | 0.0119112 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926119 | AATAAAACAGTATCA[A/G]TAAACCAACAAGAAT | 9169 |
rs372301142 | snp | C/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925359 | GGTGTTCGAGAGCAG[C/G]CTGGCCAACATGGTG | 9169 |
rs372313182 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966220 | ATGTTTAGCTTGGAA[A/G]AACAGAAAGCTTAAG | 9169 |
rs372342801 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967002 | TATCCCTTTATGTAA[C/T]GCAATGATTTATTTG | 9169 |
rs372369606 | snp | C/T | 1.64784e-05 | 0.00287035 | missense | SCAF11 | GRCh38.p7 | 12:45927584 | TCACTAAAATGCTTC[C/T]GAATCTGTTCAATGT | 9169 |
rs372396590 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45960138 | CATCATCTACAACCC[A/G]TAATTCCACCTCTAG | 9169 |
rs372411190 | in-del | -/A | 0.0225045 | 0.103662 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961437 | CTGCATTTCTACCAG[-/A]AAAAAAGTTTGATCT | 9169 |
rs372418391 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980484 | TAACTTCATTTTACA[C/G]TGATACTGTCATTAC | 9169 |
rs372526940 | snp | G/T | 5.28183e-05 | 0.00513871 | missense | SCAF11 | GRCh38.p7 | 12:45931602 | CAACATTCCAGGGTA[G/T]AAAACCAATTCTGAA | 9169 |
rs372540931 | snp | A/C/G | 0.000275113 | 0.0117255 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964209 | AGATAAATTATAATA[A/C/G]AGAATTTTATGTTTG | 9169 |
rs372580883 | snp | A/G | | | missense | SCAF11 | GRCh38.p7 | 12:45927101 | GTAGTATCCCTTTTT[A/G]GAGACCGAGACTGAG | 9169 |
rs372602350 | snp | C/T | 1.64749e-05 | 0.00287005 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922959 | TCTTCGAGCTATCTG[C/T]GCTGGCTTCCACTGC | 9169 |
rs372664641 | snp | A/C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967600 | AGTGAATCGAGATTG[A/C/T]GCCACTGCACTCCAG | 9169 |
rs372694410 | snp | A/G | 0.000165757 | 0.00910224 | missense | SCAF11 | GRCh38.p7 | 12:45948530 | CTCAGCTGTTTTTTT[A/G]CTTGAACCTATGAGA | 9169 |
rs372730386 | snp | C/T | 1.65523e-05 | 0.00287678 | missense | SCAF11 | GRCh38.p7 | 12:45927815 | AATTGAACCTCTGGG[C/T]TCTTAACAGATTGTC | 9169 |
rs372902559 | snp | C/G | 0.000153988 | 0.00877328 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922086 | ACACAGGTTCTTCCA[C/G]AGTTTTCTTTTGGCT | 9169 |
rs372919788 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952372 | TAACAGAATAATATG[A/G]ATAAGAGTTTTTTAC | 9169 |
rs372920630 | snp | C/T | 1.64789e-05 | 0.0028704 | missense | SCAF11 | GRCh38.p7 | 12:45928605 | CCTGTCTTGTTTGCT[C/T]TTCTGACTCAGCTGA | 9169 |
rs372937989 | snp | A/G | 0.00755907 | 0.0610114 | utr-variant-3-prime | SCAF11 | GRCh38.p7 | 12:45919234 | TTCATAATACAAACA[A/G]TATCTCATGGACCCT | 9169 |
rs372963080 | snp | A/G | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990756 | CCCAGTTGGGCCGCA[A/G]GGGGGCGCTGGCAAA | 9169 |
rs372968920 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934341 | AACAGGTAAATAATA[A/G]TTATACTTAAATATT | 9169 |
rs372969153 | snp | A/G | 0.00779849 | 0.061955 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934313 | AAAGTAGTTAGTGAA[A/G]CAGCAAATAAATAAC | 9169 |
rs373045355 | in-del | -/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921078 | ATCCCCGCCTCCCGG[-/G]TTCAACTGATTCTCC | 9169 |
rs373094147 | in-del | -/AGTAAAGT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989821 | GAGAGGTCACGGCGT[-/AGTAAAGT]TTGGTTTCACTAGCG | 9169 |
rs373135727 | snp | A/C | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939506 | TTTGAGACCAGCCTG[A/C]CCAACATGGTGAAAT | 9169 |
rs373464711 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972617 | AAAAAATCCAAAAAA[A/C]AAAAACAAAAACATC | 9169 |
rs373479291 | snp | A/T | 0.000133925 | 0.00818196 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951749 | AGTGATTAACAAATT[A/T]TATCTTTACAAATGT | 9169 |
rs373512205 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984046 | TTTAAAAGAACACGT[C/T]TGTATGCTGCTATTC | 9169 |
rs373513365 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947443 | AACATAAACACTTGT[G/T]ATAGTAGACAGCAAG | 9169 |
rs373532309 | snp | C/G | 0.000429859 | 0.0146542 | missense | SCAF11 | GRCh38.p7 | 12:45926571 | CTTCCCAATGAGACT[C/G]TTTCAACTTTTCTGG | 9169 |
rs373548102 | snp | C/G/T | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990168 | CCGCAGCCTCCCCCA[C/G/T]TTCGAGAGGTAGCTC | 9169 |
rs373659858 | snp | C/T | 1.70624e-05 | 0.00292077 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923200 | ATTACTTGTACTCGA[C/T]AGAAGTCTTTTAGTG | 9169 |
rs373661725 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991165 | AATTTGGAAGCCCAC[C/T]TTTCCTCCTTTCTGG | 9169 |
rs373694390 | snp | C/G | 1.64762e-05 | 0.00287016 | missense | SCAF11 | GRCh38.p7 | 12:45924937 | GAGCATGAACACCCA[C/G]TGGATATGGGAAGAT | 9169 |
rs373720556 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970881 | TCTCTAAAATTCTCG[C/T]GCAGTGTGGAAGCGA | 9169 |
rs373741424 | snp | A/G | 9.89674e-05 | 0.00703377 | missense | SCAF11 | GRCh38.p7 | 12:45927108 | CCCTTTTTGGAGACC[A/G]AGACTGAGATTGCCT | 9169 |
rs373756174 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923742 | GGCTGGAGTGCAGTG[A/G]CGCGATCTTGGCTCA | 9169 |
rs373764342 | snp | C/T | 3.31851e-05 | 0.00407326 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961762 | TTTCTGGAAAACCAA[C/T]TTCCTTTTCTAATAG | 9169 |
rs373849140 | snp | A/G | 3.46915e-05 | 0.00416468 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934152 | AAGTATAAACAGCAT[A/G]AATTAAAAGTAGAAA | 9169 |
rs373980959 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940849 | ACTCTGGCGCCCACG[A/C]TGGAGTGCAGTGGCA | 9169 |
rs374081483 | snp | C/T | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951096 | TACAAATCATAATCA[C/T]GGCTCACAACAGTAA | 9169 |
rs374090899 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919760 | ACTTGTTACTGTCAC[A/G]GAAATAATTCATGGG | 9169 |
rs374112692 | snp | C/T | 6.6012e-05 | 0.00574471 | missense | SCAF11 | GRCh38.p7 | 12:45927263 | GATGGAGACTGGGGC[C/T]GCTTCTTTTCTTGTG | 9169 |
rs374259840 | in-del | -/CAAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938516 | AAACAAACAAACAAA[-/CAAA]AAACACACTTTTCTT | 9169 |
rs374268135 | snp | A/C | 0.0021709 | 0.0328745 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945212 | ATTAAAAAACAACAA[A/C]AAAAAAGGTAGAATC | 9169 |
rs374278299 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986450 | ATTCAAGCTATCCTC[A/G/T]TCTCTCCCAGACTAC | 9169 |
rs374300336 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930232 | TCTTCTTATAAAGCC[A/G]TAATTTTGCTTCTTG | 9169 |
rs374303654 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981582 | TTTTTATCTCATTTC[C/T]CCAAGTTATTCTAGT | 9169 |
rs374313444 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921780 | TCCAGTATCCACACT[A/G]TAACACAGTCCTAGT | 9169 |
rs374348680 | snp | C/T | 1.65102e-05 | 0.00287312 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928822 | CTTTTCTTCCCCTTC[C/T]TGAGTATGTGCTAAT | 9169 |
rs374357737 | snp | A/T | 1.67049e-05 | 0.00289002 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945215 | AAAAAACAACAAAAA[A/T]AAAGGTAGAATCCAC | 9169 |
rs374369236 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956143 | TCTAATTTCTCGCTT[C/T]CTCCTGCTGCTCTAT | 9169 |
rs374422916 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938101 | CAATTTACCATCCCC[-/C]TCATACTGTTTTACT | 9169 |
rs374494263 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987427 | ATTAACTTACACTGA[A/C]GGCATTGTTCAGGTG | 9169 |
rs374565356 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921690 | AATGCATTATATATA[C/T]CTCTTTGAAAACCAG | 9169 |
rs374577372 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969136 | TAAAAATATATTTAA[C/T]AGCTGCACTGCTACT | 9169 |
rs374605780 | snp | C/T | 6.59935e-05 | 0.0057439 | missense | SCAF11 | GRCh38.p7 | 12:45926960 | TCTCTATCACTTTCT[C/T]GTTCTCTGCTCTGGG | 9169 |
rs374693059 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45928833 | CTTCTTGAGTATGTG[C/T]TAATGCATATCCCTT | 9169 |
rs374703802 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967003 | ATCCCTTTATGTAAC[A/G]CAATGATTTATTTGT | 9169 |
rs374758038 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985167 | GTAGAAAACCATGAA[C/T]TGGTACCAATTTCTC | 9169 |
rs374820834 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964679 | CTCAAAAAAAAAAAA[C/T]GGAAAGGAAAAGCCT | 9169 |
rs374835830 | snp | C/G | | | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990502 | TGACTCCGCTGGCTC[C/G]GTCCGGAGGCGGCGG | 9169 |
rs374872902 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987908 | TGGTTGTGTTTTTAC[A/G]TTATGTATTGAATTT | 9169 |
rs374889127 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958632 | CCATCTATGAATTCC[C/T]TGAAACTAAATATAA | 9169 |
rs374996692 | snp | C/T | 1.64876e-05 | 0.00287116 | missense | SCAF11 | GRCh38.p7 | 12:45926378 | TCACTCCCTGAACTG[C/T]TTGAATTCCCTGAGA | 9169 |
rs375030992 | snp | A/G | 0.000169986 | 0.00921759 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961712 | TACCTCTGCCCATTT[A/G]AGAATACAAGTCATA | 9169 |
rs375044942 | snp | C/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919724 | GTCTAACCAGTGCCC[C/G]AAATCAGACATGGAA | 9169 |
rs375180951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966291 | AGGGAGGTAGAATAA[C/T]CTATCAATGAAAGTA | 9169 |
rs375184453 | snp | A/C | 0.000218592 | 0.0104522 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922028 | ATATCCTGATAATGT[A/C]CTTGACAGCGTTCCC | 9169 |
rs375299147 | snp | C/T | 3.34655e-05 | 0.00409043 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951620 | CAATTAATTTTTATA[C/T]AATTCATGTTGCAGA | 9169 |
rs375334328 | snp | C/T | 3.33661e-05 | 0.00408436 | missense | SCAF11 | GRCh38.p7 | 12:45926165 | GATGTTTCCTCCTCT[C/T]GTTTCATCCATCCAG | 9169 |
rs375362868 | snp | A/G | 1.66679e-05 | 0.00288681 | missense | SCAF11 | GRCh38.p7 | 12:45924756 | CCATCTGGTTGTGAA[A/G]CAATGTAGTTGACTT | 9169 |
rs375497718 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977052 | CATAATTTCCCTGGT[A/G]AATTCTAAGAAATAT | 9169 |
rs375505922 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959137 | TCCTAACTGCAAATT[A/G]TACTGTTCTCTTATG | 9169 |
rs375546535 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925416 | AAAAATTAGCCAGGC[A/G]TGGTGGTGAGCGCCT | 9169 |
rs375573595 | snp | C/T | 1.64974e-05 | 0.00287201 | missense | SCAF11 | GRCh38.p7 | 12:45927087 | TTCTGCTTTCCCTAG[C/T]AGTATCCCTTTTTGG | 9169 |
rs375594015 | in-del | -/CT | 0.0275645 | 0.114116 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939526 | CATGGTGAAATTCCC[-/CT]GTCTCTACTAAAAAT | 9169 |
rs375603399 | snp | C/G | 1.64947e-05 | 0.00287177 | missense | SCAF11 | GRCh38.p7 | 12:45927112 | TTTTGGAGACCGAGA[C/G]TGAGATTGCCTCCTT | 9169 |
rs375686803 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972623 | TCCAAAAAACAAAAA[A/C]AAAAACATCAACATT | 9169 |
rs375729000 | in-del | -/AATC | 0.0154538 | 0.0865337 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993127 | AGGTACAGAGTTCTA[-/AATC]AATAAAAGATGGGCT | 9169 |
rs375742022 | snp | C/T | 6.62109e-05 | 0.00575335 | missense | SCAF11 | GRCh38.p7 | 12:45927822 | CCTCTGGGCTCTTAA[C/T]AGATTGTCTGTCCAC | 9169 |
rs375743973 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947286 | CCAGTGTACTACTCA[C/T]ATTCAATTTACCTCA | 9169 |
rs375769159 | in-del | -/CAAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978913 | AAACAAACAAACAAA[-/CAAA]AGACACTTGAGACAG | 9169 |
rs375848773 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985927 | TTGACCCAACTCTCT[C/G]TTCTTGACTTCTATC | 9169 |
rs375854741 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947154 | TCATAGATTTAATTA[C/T]GAATCTGACAACATA | 9169 |
rs375855494 | snp | C/G | 0.00720886 | 0.0596025 | missense | SCAF11 | GRCh38.p7 | 12:45927448 | ATTATTTTCAGAACA[C/G]TGTGTCACAGAATTT | 9169 |
rs375861251 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956102 | ACAAGAAACCTTCCT[C/T]ATTTGGGAATTCAGG | 9169 |
rs375862247 | snp | C/G/T | 5.14781e-05 | 0.00507315 | missense | SCAF11 | GRCh38.p7 | 12:45931524 | AATGTTCGAAAGATA[C/G/T]GGTACTTGTTGGAAA | 9169 |
rs375869562 | in-del | -/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983647 | AATTAGGTGAGGAAA[-/T]TTGAGATACTGATTA | 9169 |
rs375895994 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960729 | GAACTCAGCCAGAGT[C/T]ACTATACAGTTACAT | 9169 |
rs375919395 | snp | C/G | 6.59011e-05 | 0.00573988 | missense | SCAF11 | GRCh38.p7 | 12:45928760 | GGAGTTGTCATTGCA[C/G]GTTTTCGTCTTGATC | 9169 |
rs375954137 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945168 | CCAGCCTGAAGTGTT[A/G]CTGATGAGAACTCTG | 9169 |
rs375990494 | in-del | -/A | 0.390464 | 0.206809 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972586 | AAAACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 9169 |
rs376102199 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955387 | CTCCTGAGCTCAAAG[C/T]GATTGGCCCACCCCG | 9169 |
rs376128385 | snp | C/T | 0.000178847 | 0.00945471 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964125 | CCATGTCTTCATACT[C/T]CTTATCTCCCATATT | 9169 |
rs376183351 | snp | A/G | 0.000317299 | 0.0125916 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945216 | AAAAACAACAAAAAA[A/G]AAGGTAGAATCCACA | 9169 |
rs376228492 | in-del | -/GTT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930440 | AGGTTTTGCGTTGTG[-/GTT]TTTTGTTTTTTTTTT | 9169 |
rs376246573 | snp | A/G | 4.94417e-05 | 0.00497176 | missense | SCAF11 | GRCh38.p7 | 12:45927428 | GCAAGATCAGAAGAC[A/G]GCATATTATTTTCAG | 9169 |
rs376290267 | snp | C/T | 0.000153988 | 0.00877328 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926314 | ATCAAATGAGAACTC[C/T]TGTTCACTTTTTCGC | 9169 |
rs376319061 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977675 | AAAGGCACTTTTTCA[C/T]TGTCAACTTCATAGT | 9169 |
rs376328525 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919444 | CATTTCTATAAAACA[C/T]TGGTCAATGTGACTA | 9169 |
rs376371228 | snp | A/T | 1.70266e-05 | 0.00291771 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951762 | TTATATCTTTACAAA[A/T]GTTTCTTTAGATCAA | 9169 |
rs376431197 | snp | A/C/G | 8.24292e-05 | 0.0064194 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45922135 | GTATTTGTCTACATA[A/C/G]GCTTTAACCAGATTT | 9169 |
rs376431629 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980988 | TAGAATAGTTTGTTT[-/T]AGGGAAACAGGGCAG | 9169 |
rs376607765 | snp | C/T | 0.000181259 | 0.00951824 | missense | SCAF11 | GRCh38.p7 | 12:45927563 | GGTATCATTTCATTG[C/T]TGTCCTCACTAAAAT | 9169 |
rs376612166 | snp | C/G | 5.02063e-05 | 0.00501005 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961714 | CCTCTGCCCATTTAA[C/G]AATACAAGTCATACA | 9169 |
rs376623814 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988566 | ACACTAGCCCTATTA[C/G]CACATGAAGGTATTA | 9169 |
rs376651498 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959785 | ATAGATTGCTCTCTT[A/G]TTACTGCTCAACTGA | 9169 |
rs376677169 | snp | C/T | 3.30896e-05 | 0.00406739 | missense | SCAF11 | GRCh38.p7 | 12:45927654 | GCGATTCATTCTTTT[C/T]TTCTAAAGATTTTTC | 9169 |
rs376692419 | snp | G/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962333 | ATCTATTGATGGACA[G/T]TCACATGTTTTCAAC | 9169 |
rs376746229 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931478 | TAATAATAATTTTTA[A/T]AATAGAAAATGATTT | 9169 |
rs376773630 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923899 | TCTGTCACCCAGGCT[C/G]GAGTGCAGTGGTGCA | 9169 |
rs376796409 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939788 | ATCTAACCAATCAAT[A/C]CTAGATAAAGAGACA | 9169 |
rs376865144 | snp | A/G | 6.58913e-05 | 0.00573945 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922997 | ACTTTGCTTTCTGCC[A/G]ATTTTACAGCAGCAT | 9169 |
rs376955731 | in-del | -/C | 0.0271762 | 0.113356 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938050 | CTTAACTCCATTCTT[-/C]CCATGAAATGTCTAT | 9169 |
rs377032553 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974868 | TATCCATCCAAGAAA[C/T]CACTGTCTGAAGCAG | 9169 |
rs377039268 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947922 | GCTCAAGTGATCCTC[C/T]CACCTCAGTCTCCCA | 9169 |
rs377039359 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922607 | AGAAAATGTATAATT[C/T]ATTATTTGCCAGTCA | 9169 |
rs377061077 | snp | A/G | 7.167e-05 | 0.00598581 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934330 | AGCAAATAAATAACA[A/G]GTAAATAATAGTTAT | 9169 |
rs377072954 | snp | A/G | 0.000255787 | 0.0113061 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933240 | ATTCTGTACTAAAAG[A/G]TAAATTTTAGACCTT | 9169 |
rs377131723 | snp | A/G | 0.000132962 | 0.00815251 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934208 | AAAGGAAGATTCTCC[A/G]GAGTGGCTAACAGAA | 9169 |
rs377187424 | snp | C/T | 5.69795e-05 | 0.00533728 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948541 | TTTTACTTGAACCTA[C/T]GAGAAAAGCAAAATC | 9169 |
rs377211753 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990819 | GAGTCACGTCACGCG[A/G]CCTGTGAGCGGGAGG | 9169 |
rs377258916 | snp | A/G | 0.000181215 | 0.00951706 | missense | SCAF11 | GRCh38.p7 | 12:45926754 | CATTCTTTCTGTACC[A/G]ATCATTTCCTCGTGG | 9169 |
rs377317769 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970085 | ATTTTTAGGAGAGAC[A/G]GGGTTTCACCATCTT | 9169 |
rs377343046 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45944786 | AATATGTTAGAGGTG[C/G]TTTTATTTCTAAAGT | 9169 |
rs377398379 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957803 | TTAAGAACTCTTAAA[C/T]GCTTTAAACATGTGT | 9169 |
rs377666784 | snp | C/T | 0.000181466 | 0.00952365 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923127 | GTGTACTCATGTTAT[C/T]ACTTACATGAGAAGA | 9169 |
rs377690859 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991454 | GCGGTCCCAGCTCCT[C/T]GGGAAGATGAGGTGG | 9169 |
rs377736896 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972894 | TAGATATATATATAG[-/AT]ATATATATATATAGA | 9169 |
rs386762715 | multinucleotide-polymorphism | AGA/TAT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979203 | TCCATCCATGAGGGC[AGA/TAT]GCCCTCACAGCCTAA | 9169 |
rs397720602 | in-del | -/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944790 | TGTTAGAGGTGCTTT[-/T]ATTTCTAAAGTTTCA | 9169 |
rs397849870 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954947 | CCCCCCCTTTTTTTT[-/T]CCTTAAGCATAATTG | 9169 |
rs397850002 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945556 | TTTTTTTTTTTTTTT[-/T]GAGACAAGATTTTGC | 9169 |
rs397961653 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932360 | GATTCAATATAAGGT[-/T]AAGATTCTGGAGTAG | 9169 |
rs527361834 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969973 | CGCATCTCAGCTCAC[C/G]GCAACCTCCGCTTCC | 9169 |
rs527364221 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981491 | TCTCCCAAAAAGATC[A/C]AAAAACCGAAACATC | 9169 |
rs527403636 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921004 | TTCTTTTTTTTGAGA[C/T]GGAGATTTGCTCCTG | 9169 |
rs527410529 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980782 | TGAGTGACTCTCATG[C/T]CCTTTTAGTGCAAAG | 9169 |
rs527467738 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958287 | CATAATTGTCACTAC[C/T]ACAATGTGTGTCAAG | 9169 |
rs527633107 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949320 | AGTATAAAATAGACA[C/T]AAGATTTCAAAGACT | 9169 |
rs527636777 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957583 | TTACTCTCTCATACT[A/G]AAGCTGTTGGCATTT | 9169 |
rs527694466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956783 | AACTACCCATACAGA[C/T]CATTTTACATATTCT | 9169 |
rs527819598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972118 | AAACTGAAATATAAG[A/G]TAAACCTCCACACAT | 9169 |
rs527821452 | in-del | -/AA | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920608 | TAGTATTAAAAAGAG[-/AA]AAAAAAAAAAACCCA | 9169 |
rs527821523 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964254 | TATCAATTAAAAAAA[A/C]ATCCTAAACTGTAAG | 9169 |
rs527843313 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935639 | GCATTCACTCAACAC[C/T]TAACGAGTATGTAGT | 9169 |
rs527876846 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979842 | CCTATGAAATACAAC[C/T]CTAACCCAGATACCG | 9169 |
rs527884037 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971311 | TTACATTCCAAAATA[C/T]ATCAAAAGTGAGATC | 9169 |
rs527946353 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991719 | CAAAGTCACTGATTA[C/T]TTAACCTCCTAGTTT | 9169 |
rs528008533 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986873 | TTCTCCTCCCACCAA[A/G]ATTCTGAGGCCTCCC | 9169 |
rs528025452 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946124 | GCAAAGAAAGCATGA[C/T]TAGTTTCACTCCTCA | 9169 |
rs528079017 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987982 | CACAACTTAAAAAAA[C/T]ACAATGCAAAGATGA | 9169 |
rs528089533 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953276 | TGCATTGTCTAGTTC[A/G]AAGAACTTAACATCA | 9169 |
rs528092496 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932329 | ATTCATTTAGGTCTC[C/T]TAACAAAAGACTATC | 9169 |
rs528292430 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976137 | AAGATAACTGCAACA[C/T]AAAGGGGGAAAGGTA | 9169 |
rs528300713 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968083 | AAGTTAGATATATCT[C/T]AATTTTGTGTTATTA | 9169 |
rs528404494 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983150 | ACTTCAAGTCTATCT[C/T]TCTCCCATTTATTTG | 9169 |
rs528459793 | snp | A/C | 0.0023933 | 0.0345097 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990791 | TGTTTGAGACCGAGA[A/C]GCGTGGTGGGTGGAG | 9169 |
rs528520923 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935859 | AGTATTCGATACTGG[C/T]GAATTTGTCTAAATT | 9169 |
rs528582158 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944229 | TCTACAGCAATGACA[C/T]AGAAAAGCAAAGACT | 9169 |
rs528625515 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951526 | TTTATCATGCTAAGG[A/G]GGATTAAAATAACAT | 9169 |
rs528653880 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938980 | ATTAAAAACAAAAAT[A/G]TATAATTCAGTTATC | 9169 |
rs528664518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934872 | AATATCAATAATACA[C/T]TTAACATTTCTTTTC | 9169 |
rs528670477 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958904 | TGGCCAAAATAAATA[C/T]ACTAGACTACGACAC | 9169 |
rs528687303 | snp | A/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925612 | CATGCAAAACATACA[A/T]CAACAATCAGTAGCT | 9169 |
rs528731784 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967081 | GCAAACTAACCTGAT[A/G]TATAATTTATAATTT | 9169 |
rs528743644 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | SCAF11 | GRCh38.p7 | 12:45926336 | CTTTTTCGCTTATAG[A/G]ATTGCTGTTCCACAA | 9169 |
rs528758970 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958409 | TAAAATAAATAACTT[C/T]CTAACTGAATAGATG | 9169 |
rs528800998 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966475 | AATAGTAAGTAAAAT[A/G]TCTAGTATGTTAGAC | 9169 |
rs528841210 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993329 | AGCAACAGAAACCCA[C/T]AGTGGCACGTTTAAA | 9169 |
rs528876042 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987374 | TTTCAAACCACAATC[A/G]CTATTTGTAACGTTT | 9169 |
rs528889000 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959717 | CTGAAAACTTAGTCT[A/C]CATGATTTTTTTAGC | 9169 |
rs528921590 | in-del | -/AC | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985860 | GAGCTTCACATTGTT[-/AC]ACTCAACAGAATTTT | 9169 |
rs528972716 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967949 | TTGCTTTGAATATCC[A/C]GTGACAGGAACACAG | 9169 |
rs529031026 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975133 | AAACCATGCTGTAAA[C/T]GGATGTGCTGTCATC | 9169 |
rs529045850 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969975 | CATCTCAGCTCACCG[C/T]AACCTCCGCTTCCCA | 9169 |
rs529081882 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929227 | CACTGGAGCAATCAT[C/T]GCGCACAGAAGCCTC | 9169 |
rs529095888 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974673 | ATAATAGTTCTCCTG[C/T]TGTTTATACCACACC | 9169 |
rs529195029 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990218 | CGACGTCGCACGGGC[C/T]GCGCGAGATTCCGAA | 9169 |
rs529218134 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921915 | TAGAACAAAACATCA[C/T]ATCCTATGTTAAAAA | 9169 |
rs529272052 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989790 | GAAGCGCCGGCTCTT[C/T]CCCATTCGCGCACTC | 9169 |
rs529327311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951439 | ACAAGGTGATCATTA[C/T]GGATATGCCCTCTTT | 9169 |
rs529387396 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951021 | TCCTTTTCTCTTTTC[C/T]TCTTACTCAACTCAG | 9169 |
rs529419708 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958912 | ATAAATATACTAGAC[A/T]ACGACACACTTTAAT | 9169 |
rs529518942 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973951 | TTGAATTCTTTAAAA[C/T]AGGTTTGGCATTAAA | 9169 |
rs529579327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973142 | AACAACCAAATGGAA[A/G]CCAACAAAAAGTGAA | 9169 |
rs529650324 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986283 | CTGATATGTTAAAAC[C/T]AAAAGAGCTCTGGTC | 9169 |
rs529657891 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924155 | CTAGGATTCTAAAAT[A/T]TTTAAAAGGCAGTCA | 9169 |
rs529672529 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940504 | TATAGAGTCAGAAGA[C/G]TGGATCAAATTCTGG | 9169 |
rs529696131 | snp | C/T | 0.0023933 | 0.0345097 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993898 | GTTTCTATAAGAGGA[C/T]ATTTTTATTTTAATG | 9169 |
rs529758478 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938538 | ACTTTTCTTTCATTC[C/T]TTTATTGTCATTTTA | 9169 |
rs529907714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970070 | CCAGCTAATTTTTGT[A/G]TTTTTAGGAGAGACG | 9169 |
rs529911999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963101 | AGGAGACAGAAAAGG[A/G]AATATAAGACATAGC | 9169 |
rs529921156 | snp | A/G | 6.82152e-05 | 0.00583977 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961869 | TCACCTGTTAAAGTA[A/G]AACAGCCATATGTGC | 9169 |
rs529938794 | snp | C/T | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918663 | AGTGAGCTGAGATGG[C/T]GCCACTGCATTCCAG | 9169 |
rs529969808 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969499 | GGTTAATACTACAAA[C/T]TTTAGAATCCAACAG | 9169 |
rs529999420 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985963 | GTAACATTCTCTTTC[G/T]TTGGTTTCTGTAACA | 9169 |
rs530030788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976921 | CTTTGAAAAGATCAA[C/T]AAAATTTAAACCTCT | 9169 |
rs530055966 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976944 | AAACCTCTTGCCAGA[A/C/T]TGATGATGTAGATAG | 9169 |
rs530094371 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976280 | TTAGTCAACGTCTTG[C/T]GTCGTTCCACCTTCA | 9169 |
rs530110795 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954040 | GACGTAGATGGAAAT[C/T]CAAGTACTTCATTAT | 9169 |
rs530124246 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982505 | TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGACCA | 9169 |
rs530156221 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984280 | GCAAAATGTCTTCCA[A/G]TTTGGGTTTGCCTGA | 9169 |
rs530163346 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919385 | AAAAGCACAAAACTT[C/T]TGGAATGTTAATGGA | 9169 |
rs530223499 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920205 | ATTTTTATGATTACA[C/T]TCATAACAACAAAGC | 9169 |
rs530232420 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992660 | TTATATTTTAAAAAA[C/T]CTATATATATTTAAA | 9169 |
rs530368340 | in-del | -/ACC | 0.00953873 | 0.0683987 | cds-indel, intron-variant | SCAF11 | GRCh38.p7 | 12:45919811 | AGACTTCAACTCTTG[-/ACC]ACATCACTTTTTCTC | 9169 |
rs530371405 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952307 | GTGTATCTTTTTAAT[A/G]TATAAACTTAAGATT | 9169 |
rs530381199 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939180 | GTACAAAACTCAAGG[A/G]GCTTGACTTCCAGTA | 9169 |
rs530402589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953255 | AGTTCATATATTTTT[A/T]AATAATGCATTGTCT | 9169 |
rs530411269 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993228 | TAAAAAGCACAAATG[A/G]TATGCATCATAAAAC | 9169 |
rs530435429 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969386 | TGTTACAAAACAGAG[C/T]TCCTTTCCCTTCCAG | 9169 |
rs530472784 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947755 | GATCATAGCTCACTG[C/T]AGCCTCAGATTCCTG | 9169 |
rs530537675 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947231 | TCAAAATGAGCTTAA[C/G]TTTCAAATGTATTAG | 9169 |
rs530601713 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954195 | TTTCCTCTACTGACA[A/T]CAGCTAAATTGCATT | 9169 |
rs530671770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961686 | ATTAAAATACATTAA[C/T]GTGTCAGACTTACCT | 9169 |
rs530726451 | in-del | -/TAAG | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975044 | TACGTGCACTGTCAA[-/TAAG]TAAGTACTATGTTGA | 9169 |
rs530749480 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976250 | GTATAATTCTTAGAG[A/C]TACCACTAAAAACAT | 9169 |
rs530961136 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945026 | TTTTCTCCCAACACA[C/G]GCACACACACACCCC | 9169 |
rs530964032 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937862 | GAGTGTAAATCTCCA[C/G]TCTTTCATTGGGTAC | 9169 |
rs531027322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952118 | TTCTATGACTTAATA[C/T]TTTCCCCCCAAATTA | 9169 |
rs531043703 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957959 | GTGCAGTGGCATAAT[C/T]ACAGATAAATGTAGT | 9169 |
rs531081583 | snp | A/G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933790 | CAAATTCCATAAATA[A/G/T]CAACTTAGTATCTAC | 9169 |
rs531149878 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959119 | AGAAATCTAGAAAGA[C/G/T]GATCCTAACTGCAAA | 9169 |
rs531184493 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931034 | TCTTTAGAACTTATT[A/C]TATCCAGCTGAAACT | 9169 |
rs531200017 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924546 | TTTAATTAATTTTCT[A/T]ATTTGGGAGTTGGGG | 9169 |
rs531212282 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989435 | AAATGAATGAACAAC[A/G]GTCAGCTGGTAGACA | 9169 |
rs531290969 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970173 | TGCTGGGATTACAGG[C/G]ATGAGCCACCGCGCC | 9169 |
rs531299620 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941918 | TTTCTGCCATTGCCA[A/T]CCAAGACAGCAAGAC | 9169 |
rs531347378 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973035 | AGATATATAGATATA[G/T]ATATATAGATATATC | 9169 |
rs531397031 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967884 | CTGTTCTATCTGCCT[C/G]GACTCCAGTTTTCAA | 9169 |
rs531425950 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940759 | ATGAAAAAAACTTTT[A/C]ATTGTGTCTACTTGC | 9169 |
rs531490852 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967572 | TTGCTTGAACCCAGG[A/T]GGCGGAGGTTGCAGT | 9169 |
rs531544857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955751 | TATATACAACAAAAT[A/G]TCCTTCAATGACTCA | 9169 |
rs531671186 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920560 | GGCACAATAAACATT[G/T]TAAACTTACCTTTTA | 9169 |
rs531681860 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963319 | TAAAACTGTAAAATA[C/T]CAAAGACGAAACCAA | 9169 |
rs531815847 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977029 | CAAAAAAGAAACCTC[C/G]AGGCCCACATAATTT | 9169 |
rs531876582 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978709 | GGAAAACTGTCAACT[A/G]TATTTTTACTTCAAC | 9169 |
rs532002093 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979236 | TCACCTCCTAAAAGC[C/G]CCACCACTTAATACT | 9169 |
rs532002598 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986134 | GCAATTTCATCCATA[A/C]CTATAGTTCCAATTA | 9169 |
rs532024526 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939699 | CCTGGGCAACAAGAC[C/T]GAAACTCCATCTCAA | 9169 |
rs532030458 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987134 | GGGAGGCCAAGGCGG[A/G]ATGATTACTTAGCCC | 9169 |
rs532036449 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941132 | AGCATAAATAAACAT[A/G]TATCAACACAAACTG | 9169 |
rs532145147 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924372 | CTAGTTCCCACCGTC[C/G]CCATATACCCCCTAA | 9169 |
rs532249589 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963989 | AGGCAGCTTATTTTG[G/T]AATTTAAGAACAACA | 9169 |
rs532380500 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934028 | TAGAGCTAGTTTACC[G/T]TCCCCCCCGCCCAAA | 9169 |
rs532436221 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973818 | ATGATGAGAATTCTT[C/T]TCCAGCTCTAAAAAA | 9169 |
rs532441757 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934928 | CTATCTCAAGCAGGG[G/T]CTGACTAGGTGGCCT | 9169 |
rs532455793 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985143 | CTCTAATTATTTCAA[C/T]GTCTATGTGTAGAAA | 9169 |
rs532498633 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970283 | GCAATCTTCCCACCT[C/T]GGTCTCCTAAAATGC | 9169 |
rs532518090 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982384 | TCTAGGCATACAAAA[C/T]AGTGCTATACGTATA | 9169 |
rs532544214 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970185 | AGGCATGAGCCACCG[C/T]GCCCGGCCTCAACTA | 9169 |
rs532565028 | snp | C/T | 1.65059e-05 | 0.00287275 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927250 | TTCTCTTCTGGGAGA[C/T]GGAGACTGGGGCCGC | 9169 |
rs532593689 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938930 | CAAACCAAAGATTAA[A/T]GTTCATTCCAAGAAA | 9169 |
rs532615580 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949591 | GGGATACAGAAGAAA[A/C]ATATTTAAGACATTG | 9169 |
rs532624018 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948710 | TAAGCTTAGTAAGTA[C/T]GCTTAGGTCTGGGGA | 9169 |
rs532655979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938194 | AAACTTTGTGGCTTA[A/G]AACTCTTCTTTCTGG | 9169 |
rs532657300 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | SCAF11 | GRCh38.p7 | 12:45919145 | ATTAGTTTATCAAAA[G/T]AATTTATTAGAAAAT | 9169 |
rs532743294 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985146 | TAATTATTTCAATGT[C/G]TATGTGTAGAAAACC | 9169 |
rs532752143 | in-del | -/GCTT | 0.00199481 | 0.0315187 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918989 | TATAGCTAACTCTAA[-/GCTT]GCTTTAGAGCTTGGG | 9169 |
rs532800329 | in-del | -/A | 0.00134469 | 0.0258947 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945210 | AATTAAAAAACAACA[-/A]AAAAAAAAGGTAGAA | 9169 |
rs532806848 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992951 | GTTTCTACCTTCATG[C/T]GCAAATAGAAGAGAG | 9169 |
rs532854156 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974632 | GCAGCAATTCAGTCA[A/T]GTCTTCAGGCTCCAC | 9169 |
rs532870660 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991984 | GCCACCCTGACGCCT[C/G]CCCGGGATGAGTTTC | 9169 |
rs532900040 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930374 | ACTTTTTACTGTGAT[A/T]TGCAATCTATTAGAA | 9169 |
rs532961202 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931118 | TACAATCTAGTTCTA[C/T]GAGATCAACTTTTTT | 9169 |
rs533009813 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966622 | TTGAACTGGCAATCA[C/G]AAAGCAGCAAGGGAG | 9169 |
rs533066719 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942725 | CACTGCTCAAATATA[C/T]CTTTATTCAAGAGGG | 9169 |
rs533085794 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982331 | AATATTTATTCCCCA[C/T]TATAACAGCTTACAG | 9169 |
rs533127354 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950926 | TTATATTGAGTACTC[A/T]CATTTTTAGCTATTT | 9169 |
rs533218274 | snp | C/G | 4.95577e-05 | 0.00497759 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923138 | TTATTACTTACATGA[C/G]AAGAACTAGGAATAC | 9169 |
rs533313121 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942220 | ACTGATTTCTGACTG[C/T]GCAGGGGTACCCCTA | 9169 |
rs533334818 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45928074 | TTGGAAGATGAACTG[C/T]ACATACATCTGTCTT | 9169 |
rs533361918 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972975 | ATATATATATAGATA[C/T]ATAGATATATAGATA | 9169 |
rs533372468 | in-del | -/A | 0.00993419 | 0.0697739 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925390 | AACCCCGTCTCTACT[-/A]AAAAAAATACAAAAA | 9169 |
rs533445977 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957713 | AAATATTTTATATTA[C/T]GTAAAAGGGAAAAGA | 9169 |
rs533496164 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964528 | AAAAATTAGCCGGGC[A/G]TGGTGGCAGGTGCCT | 9169 |
rs533507417 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925992 | GTACGTGTATATATA[-/T]TTATATAATGCTAAG | 9169 |
rs533509773 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956817 | ATTTAAAACTAGGCA[C/T]AAAGAAATGCATGTT | 9169 |
rs533540528 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966728 | AAGGCATGTCTGGTA[C/T]GTTCAAGGAACAACA | 9169 |
rs533638980 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972165 | TGGGTAGCGCATATT[C/G]AAAAAGTATAAATAG | 9169 |
rs533671200 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972575 | GATGCGACAGCAAAA[C/T]CCTGTCTCTTAAAAA | 9169 |
rs533686692 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932109 | ATTTCTGCCCCCCTA[C/G]AAAGTGTCCTCACAC | 9169 |
rs533702909 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923861 | TAATTTTTGTATTTT[G/T]TTTTTTCTAGACAGA | 9169 |
rs533731833 | snp | A/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992389 | AACAACAAAATTCTT[A/G]TGAAGGACCTTTCCC | 9169 |
rs533741149 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980225 | CACCAGAAATCATGA[A/G]TATTCAAACAACAAG | 9169 |
rs533878772 | snp | A/C | 0.000399281 | 0.0141238 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918720 | TCAAAAAAAGAAAAA[A/C]AAAGAGAATATTATA | 9169 |
rs533924375 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934347 | TAAATAATAGTTATA[A/C]TTAAATATTTTGATA | 9169 |
rs533927714 | snp | C/T | 6.59e-05 | 0.00573983 | missense | SCAF11 | GRCh38.p7 | 12:45928718 | CTGGCTGTTTCAGCT[C/T]TTGTGTTACGTGTAG | 9169 |
rs533945683 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940042 | TTTCTGCCCCTAAAC[C/T]TTGCAATAATTCCAA | 9169 |
rs533977853 | in-del | -/ATT | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981890 | CACCAATTAAAAGAG[-/ATT]ATCAAACTGGATTTT | 9169 |
rs534024389 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951000 | TATACTTAACTACTA[C/T]TCTTCTCCTTTTCTC | 9169 |
rs534047830 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979503 | TTCAATTCCAGAAAT[C/T]AGTTTATTTTGCACA | 9169 |
rs534191561 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962496 | ACAAATTATTCTCCT[C/T]AGGATTTGTACTACT | 9169 |
rs534198570 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919436 | ATTCTAGGCATTTCT[A/G]TAAAACATTGGTCAA | 9169 |
rs534254146 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977815 | CCATTTCTTCAGCAC[G/T]GACAGTTCTGAGAGA | 9169 |
rs534272919 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937122 | CTATTACGGAAAAAA[A/T]TTCCTTTGTATTACT | 9169 |
rs534319041 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968275 | TTCTGATTATTTTAA[C/T]TTACAAATGTCAATC | 9169 |
rs534324101 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942422 | ACTCTTATTCGTCTA[C/T]GATTTTCTTCCCTTC | 9169 |
rs534324478 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923262 | GCAAACCAACCTTAG[G/T]ACTAAAGAAAAATGC | 9169 |
rs534330908 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936261 | ATTCTCCTGTCTCGG[C/T]CTCCTGAGCAGCTGG | 9169 |
rs534390651 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972280 | CAACTGGATCAACTG[C/T]CTGTAAAAATAAAAA | 9169 |
rs534450823 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974665 | CTAATTCTATAATAG[C/T]TCTCCTGCTGTTTAT | 9169 |
rs534460212 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970607 | TTCAGTTTCTAAGAA[C/G]ATTATCAGTGACCTG | 9169 |
rs534576890 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991032 | TTTGCGCAGGGTGTG[C/T]TCCTTATCTTTATGG | 9169 |
rs534626567 | snp | C/T | 0.000299083 | 0.0122251 | missense | SCAF11 | GRCh38.p7 | 12:45945300 | ATAGATCTTCTCTTA[C/T]GATGGCTTTTCTTCT | 9169 |
rs534690297 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952523 | TACTCTTTTTCAAAT[G/T]GAGTTATAGGTGCTC | 9169 |
rs534722198 | snp | A/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993076 | TATTATTCTCTCTGA[A/T]GTTTTCATATTTTTT | 9169 |
rs534733597 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984065 | ATGCTGCTATTCTGG[A/C]TGGAGGCATTGGAGC | 9169 |
rs534812363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959359 | CAGGCTATCCCTTGA[C/T]GTACTTAAAAATCGT | 9169 |
rs534845537 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924662 | GCCTTTTTTTGAACA[C/T]CTGTCATGAACAGCT | 9169 |
rs534868017 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988897 | TTTTTAAAAAACTCA[C/G]ATTGCATAAAAAATA | 9169 |
rs534875000 | in-del | -/TTTC | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954227 | TTTCCTTTACAATTT[-/TTTC]TTTATTTTTTTTATT | 9169 |
rs534879337 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958717 | TTAGGCTATGGGCCA[C/T]GAAGGCTACCACAGG | 9169 |
rs534947986 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974757 | GGGTTGGAATCAACT[C/T]CTTCACAATCCTGTT | 9169 |
rs534983109 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950549 | TTATACATACAAACA[A/G]CGTTTGGAAAAATGG | 9169 |
rs535046751 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957886 | ACTGTGGGAAATAAT[C/G]ATTCCTACTTTCTCT | 9169 |
rs535092573 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951816 | TTCCATAAAATTATT[G/T]TTATCTCTATCTTCG | 9169 |
rs535094173 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924136 | GTGAGCCACCATGCC[C/T]GGCCTAGGATTCTAA | 9169 |
rs535152834 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951195 | ACACAGTTTTCAGTT[A/C]TTTTGGACTTAAGGT | 9169 |
rs535177117 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952409 | TTCCTTTTATAGGAG[-/T]TAAGGTTGAGCACAT | 9169 |
rs535232783 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958494 | TTAATTTTAGATTGT[G/T]GGATCTAACAGTTAT | 9169 |
rs535244701 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950201 | TAAAATAAGATAATA[C/G]AGGTAAATGTTCTAT | 9169 |
rs535246795 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986937 | CTTTTTCTTCCCAGT[C/T]TCAGGTATGTCAGCA | 9169 |
rs535365190 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949859 | AAGCATCCAAATATA[C/T]GTAGTACTTAAAGCT | 9169 |
rs535378105 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957837 | CAAACCATGACCTTA[C/T]TTTAAGGGCCAAATT | 9169 |
rs535462003 | in-del | -/AGTTTCAGGC | 0.00795532 | 0.062565 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943595 | TTTGGTACTATCTGT[-/AGTTTCAGGC]ATCTACTTGGAACAT | 9169 |
rs535523558 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988736 | CAGTAAGCAAACATT[C/T]AAATTTTACCCCAGT | 9169 |
rs535574280 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952913 | CCTTTCTGGGTTTTA[A/C]CACGTATCAAGACAT | 9169 |
rs535578018 | snp | C/T | 0.000148408 | 0.0086129 | missense | SCAF11 | GRCh38.p7 | 12:45928251 | CCTCACCAACTAGCA[C/T]AGGAAGATCTTGAGC | 9169 |
rs535650938 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920683 | ATTTCCCCTCTGTTT[C/G]TAAAACACAGGTTTT | 9169 |
rs535700011 | in-del | -/T | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977070 | TCTAAGAAATATTTA[-/T]AAGGAGAAATAACAC | 9169 |
rs535701319 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966036 | GATGAGGAATATTTC[A/C]CACTCTTAGCCTATG | 9169 |
rs535769594 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973537 | CCATGCCTGGACACA[C/T]ATCAGAGTCAAGCTA | 9169 |
rs535897033 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980322 | TCACTATATTACTAG[A/G]ATCCAACAGCATGCC | 9169 |
rs535935396 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942304 | CATCTCCACTAATAT[C/G]TCCTTGGCCCAAGCC | 9169 |
rs535952972 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988054 | CTGGGCTCTACTCAG[A/C]ACTACTAACAGTTAT | 9169 |
rs535980346 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984798 | CTCCCAGGTTCAAGC[A/G]ATTCTTGTGCCTCAG | 9169 |
rs536000971 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950433 | CTTTTAAGTAAAATA[A/C]AAACTCTATCAAATA | 9169 |
rs536012325 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921103 | TTCTCCTGCCTCAGC[C/T]TCTCGCATAGCTGGG | 9169 |
rs536074062 | snp | C/T | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918837 | GTGCAGTTTGCTTGG[C/T]ATTAGTTATTACCTT | 9169 |
rs536124123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930598 | CAGGTGGCGGCCACA[A/G]AAATTGTTACACTGG | 9169 |
rs536129378 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949045 | AATAAGAAAATCTAC[A/G]GGCATCAGAGAGTAA | 9169 |
rs536188709 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952758 | AACTCTGCAAAGAGC[A/G]TACCAAAAGGTGATA | 9169 |
rs536201838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949112 | TTTGTTTTTAGGAAG[A/G]TAACTTTGGTGTGAT | 9169 |
rs536241429 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968817 | CGTGGTGTAATCCCA[A/G]CTACAGGCTGAGGCA | 9169 |
rs536246179 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977249 | CATTCAATCATATAA[C/T]GAAATACTGCTCAGC | 9169 |
rs536301922 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985275 | ACTCATTATCATTAC[C/T]TACTAAATTTGATCA | 9169 |
rs536305655 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968515 | CATATAAGAAGGTAT[C/T]AAAGCTTGGAATTTA | 9169 |
rs536312873 | in-del | -/CA | 0.00597247 | 0.0543191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954720 | GATACATGCATGTAT[-/CA]CACCGTGCCTAGCTT | 9169 |
rs536337979 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939367 | CACCTATGTTTAAAG[A/G]ACAGTCCCATCCTGC | 9169 |
rs536400055 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947262 | AACAAGTTATTTAAG[A/C]ATTAATTTCCAGTGT | 9169 |
rs536400336 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938352 | AAATTAGCCGGGCAT[A/G]ATGGCGGGCACCTGT | 9169 |
rs536406418 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937102 | ATCTGGACACCTGTG[C/T]TCTACTATTACGGAA | 9169 |
rs536462168 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946509 | TTATGACAAATCTCA[A/G]AAAAAGCAGTTAAAT | 9169 |
rs536463479 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933556 | AAATTCTAGGTGCAA[C/T]AGTTTCCTACTTGAA | 9169 |
rs536467996 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934087 | GCCTTTCAGTTTTTA[C/T]TGGGCCCAGAGTTTA | 9169 |
rs536468231 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970486 | TATGGATGAGCACTG[A/G]TATGATAAATGAGAG | 9169 |
rs536518466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953620 | GCTTCAAAATGTTTT[C/T]TATTCCTATTTTAAA | 9169 |
rs536526503 | snp | A/T | 1.648e-05 | 0.0028705 | missense | SCAF11 | GRCh38.p7 | 12:45924861 | AGGGGCACTCCTGTG[A/T]GGAGATGCAAGGGTA | 9169 |
rs536529975 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936149 | TGTGGTTTTTTTTGT[C/T]TTTTTTTTTTGAAAC | 9169 |
rs536572545 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979466 | GTTCTGTTTAAACAA[G/T]ATTTTTAAAACTTTA | 9169 |
rs536596122 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944406 | CATATTAATTCTAAT[A/C]AAAAACAAAGCCAAC | 9169 |
rs536656500 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921430 | CAGCATAACCTTTAT[G/T]TGGTCATACAATAGG | 9169 |
rs536717229 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922346 | CAAAAGGCAAAAAAG[G/T]AGACAGGAATTAGTA | 9169 |
rs536744520 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966491 | TCTAGTATGTTAGAC[A/G]TTGAGAAGTGCTATG | 9169 |
rs536872800 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936992 | TATGTGGTCTGTTTT[G/T]ACTCTCTCTCTTGTC | 9169 |
rs536902128 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941205 | ACATGAAATGCAAAT[A/G]TACAATTTCTTCAGA | 9169 |
rs537082875 | in-del | -/AAC | 0.00119737 | 0.0244387 | cds-indel, intron-variant | SCAF11 | GRCh38.p7 | 12:45920819 | ATCAGTGATTAGATA[-/AAC]AACAACTTTACGCCA | 9169 |
rs537089846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983904 | AAGTTTAGTCTTATC[C/T]CTAATAGAGATGTGA | 9169 |
rs537109638 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974833 | TCTAGAATGGTGAAT[A/C]CTTTCCATTACTTTG | 9169 |
rs537129977 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946269 | AGGGTTTTATTGCTT[C/T]GGAAGGGAGAGGCAA | 9169 |
rs537159756 | in-del | -/ATT | 0.00159617 | 0.0282053 | intron-variant, cds-indel | SCAF11 | GRCh38.p7 | 12:45960266 | ACTTATTACATACAC[-/ATT]ATAATTTTCTTAGAG | 9169 |
rs537173775 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982784 | CAGTGTTGTTTTGGC[C/T]GCTGTCTTTCATGTT | 9169 |
rs537192569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932618 | TTTACTTAGGAGCTT[C/G]ATTTAAGTATATATT | 9169 |
rs537234651 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990447 | TCCCCAACATGGACT[C/T]CTTCGTCCGCTTTGT | 9169 |
rs537296352 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989979 | GTGGAGCCCCTTCCC[C/G]CCCCCCCGTAGGACC | 9169 |
rs537313553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959940 | CCTACCCAGCATCAC[A/G]GTTTATAATAGCAGC | 9169 |
rs537388581 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949410 | TTGAGCTAATACATT[A/G]GATATATTGGATTAA | 9169 |
rs537565078 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970894 | CGTGCAGTGTGGAAG[C/T]GAGTGCCAAAATAAT | 9169 |
rs537575709 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974358 | AAATGAGATAACATT[A/C]AAGTATGCCACACTG | 9169 |
rs537631777 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978197 | GCATATGTCCTTTGA[C/T]AACTTCAATATATTT | 9169 |
rs537647394 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924052 | GGCAGGGTTTCACCA[C/T]GTTGGCCAGGCTGAT | 9169 |
rs537675824 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980599 | TTGACACTAAACGGC[C/T]TAATACACAAAAGGA | 9169 |
rs537730864 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929908 | GATTAGGAGCACCAA[-/C]CCCCAACACAGTCAA | 9169 |
rs537731426 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951920 | AGATAGTTGGAATAC[A/G]ATGATGAACGAGACA | 9169 |
rs537847936 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964425 | GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCGG | 9169 |
rs537858428 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947422 | GTATATTTAAAAAAA[A/T]GTTTTAACATAAACA | 9169 |
rs537918018 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954615 | CACTCTGTCGCCCAC[A/G]CTGGAGTGCAGTCAC | 9169 |
rs537969047 | snp | G/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992862 | CAGAGAATTAAGTTT[G/T]CACGTTCTTACTGTT | 9169 |
rs537984170 | snp | A/C | 4.94214e-05 | 0.00497074 | missense | SCAF11 | GRCh38.p7 | 12:45926829 | AGTAACTATCTCTGT[A/C]AATTCTACCAAATGA | 9169 |
rs538047234 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918876 | TTACAGGTGATTTTT[C/T]TCCTTTTTCAGTCTC | 9169 |
rs538091435 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986483 | AAAAAGCCTGCTAAC[G/T]AATTCTCCCAGATCT | 9169 |
rs538129997 | snp | C/T | 8.24042e-05 | 0.00641836 | missense | SCAF11 | GRCh38.p7 | 12:45928529 | GCAGCTACAGAGCTC[C/T]GAAGTTTCTTTTTCA | 9169 |
rs538185956 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964964 | ACTAAGGAGACAGTT[G/T]TGTGTGTGTATGTGT | 9169 |
rs538196231 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971271 | AACTGTATTTAACAT[A/G]AATATGAGGTGATTA | 9169 |
rs538288740 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974232 | CTCAGCAAGGCTTCA[A/G]CAAGTCATAATCTTT | 9169 |
rs538291545 | in-del | -/G | 0.00597247 | 0.0543191 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993794 | AAAAAAAAAAAAAAA[-/G]AAAAAGAAAAAAAAG | 9169 |
rs538369945 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977436 | GGTTAGGGGAATGTA[C/T]GACAACACAGTTTTT | 9169 |
rs538422658 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993915 | TTTTTATTTTAATGA[A/T]CTCTGGCATTTTTAT | 9169 |
rs538436968 | in-del | -/A | 0.00874735 | 0.0655527 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921629 | TCTATAATTAGAGGG[-/A]AAAAAATCATAAAGA | 9169 |
rs538528575 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932818 | CAGGTAAGACTGGAA[C/T]GGGAGAAGAGTAGAG | 9169 |
rs538563220 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976370 | CTTTTATTACAGTAT[A/G]TTGTTATAATTGTTC | 9169 |
rs538593668 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933379 | TTTTCTATTTAAACA[C/T]TTTCAAAATAAACTC | 9169 |
rs538598859 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946677 | ATGATACTGTCACAG[C/T]CAGTGATATGAGTTG | 9169 |
rs538607811 | in-del | -/CTCTTATT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978011 | GGTTACACTCTTATG[-/CTCTTATT]TGACAGTCATCCACT | 9169 |
rs538662948 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974333 | CAGGGTTGGCTGTGG[C/T]AATTCCTTAAAATGA | 9169 |
rs538715191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961128 | TGAAATTAGTCCACA[C/T]TAAATTAAAAACAGG | 9169 |
rs538719390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925758 | AAAAACAAGGAAATA[C/T]AAATCTTTACTATTA | 9169 |
rs538852018 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939395 | TGCTTCACAAAACTT[C/T]AAGAAATTAAAGAAG | 9169 |
rs538902074 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947392 | GTTTTAACAGCAACT[A/T]AAAAAAAGAAACCTG | 9169 |
rs538914278 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975598 | CCCTCTCAGACTTCA[A/C]TGGCTTGAAGAGCGT | 9169 |
rs539050518 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958454 | ACTGGCTCTATATAC[A/G]TTTCATCAGTTCAAA | 9169 |
rs539113163 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957911 | TTCTCTCTTTTTTTT[G/T]AGATAGGGTCTTATT | 9169 |
rs539120004 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929403 | GTTCAAGTGATCTGC[C/T]TGCCTCGGCCTCCCA | 9169 |
rs539187154 | snp | A/G | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965822 | TGAACTCCCCAGGAA[A/G]ATTCCCTATTTGGTT | 9169 |
rs539205576 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921994 | AGTTAATGGTACATG[C/T]TGAAATTGCACTTTG | 9169 |
rs539210794 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976331 | GTACAGTAAGATATT[G/T]TCAGAGAGCCCACAT | 9169 |
rs539247338 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973436 | GAAGAAATAATGGGT[A/G]GAAACTTCCTGAAAT | 9169 |
rs539528504 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949624 | CAGAAAAAAACAGAT[C/G]AGGGAGAGAAAACTG | 9169 |
rs539556365 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921251 | CCTCCCAAAGTGCTG[A/G]GATTACAGGCGTGAG | 9169 |
rs539568558 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959178 | AGGAGCTGTGGCACA[A/G]GAATCGCTTGGCCTG | 9169 |
rs539616916 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965176 | CAAGATAAAAGTGAT[A/G]TAAGTGAATTTTTTT | 9169 |
rs539680110 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972728 | CTTGGCATAGAGAGA[G/T]GTGGGAAAAATAACA | 9169 |
rs539764872 | in-del | -/AAAA | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978914 | AACAAACAAACAAAC[-/AAAA]GACACTTGAGACAGT | 9169 |
rs539766397 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980240 | GTATTCAAACAACAA[C/G]AAGTGGTAACATTCT | 9169 |
rs539795330 | in-del | -/T | 0.143622 | 0.226238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984696 | GCTCTTCGCACTTCC[-/T]TTTTTTTTTTTTTTT | 9169 |
rs539900310 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940910 | CCCAGGCTCAGGTGA[A/T]CCTCCCACCTCAGCC | 9169 |
rs539964204 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948806 | TGTATATACATATAG[A/G]ACTCAGAAATTAACT | 9169 |
rs540002455 | snp | C/T | 0.00143237 | 0.0267233 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924983 | TTGTGCATTCATTTG[C/T]TGCTGCATTACATTC | 9169 |
rs540043379 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987901 | AAAATAGTGGTTGTG[C/T]TTTTACGTTATGTAT | 9169 |
rs540048638 | snp | C/G | 2.21594e-05 | 0.00332855 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931638 | AATAAAGACATTTTT[C/G]TTTAAATGGTTTAAA | 9169 |
rs540069263 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937271 | TCTTCTACTCCTGTT[C/G]AATTTTTGTATTTTT | 9169 |
rs540103956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955259 | CCTCCTAGGTTCAAG[C/T]GATGGCCTCACCTCA | 9169 |
rs540105876 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964303 | AAGAACACAGTACGA[A/G]CCAAGCCAGTTTGTG | 9169 |
rs540106671 | in-del | -/TGGCT | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980159 | ATTAAGTAGTAGGAC[-/TGGCT]TGGAACCCATTAGCA | 9169 |
rs540110111 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923323 | TTTAAAGAAAAATGA[A/G]TAACATTCTTAAACG | 9169 |
rs540149795 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970141 | CCTCGTGATCCACCC[A/G]CCTTGGCCTCCCAAA | 9169 |
rs540165005 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963504 | CCAGTAAAACTATCT[C/T]TGAATAGTTTTAAAG | 9169 |
rs540175390 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978273 | GACAGAACACAAAGA[C/G]TTGGTTACACAATCT | 9169 |
rs540243482 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986615 | TAACAATAAGATAGT[G/T]ATACTGCTTGATATG | 9169 |
rs540287597 | snp | C/T | 1.69095e-05 | 0.00290765 | missense | SCAF11 | GRCh38.p7 | 12:45948450 | ACCTTATACAGCTTT[C/T]AGAATTTTCATGACA | 9169 |
rs540307947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924337 | CAAGACAATAAAAGC[C/T]TCATCACAGTACTTA | 9169 |
rs540317463 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933716 | TTAAATCACACAATC[G/T]TATTCTGTGCTGCTG | 9169 |
rs540366235 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938745 | ATAAAGGCTCTGAGC[C/T]TAGAACCCAGTACTT | 9169 |
rs540372905 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985115 | AAGGTATTTAGAAAA[C/G]AAGATTTGGATGCTC | 9169 |
rs540386657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934909 | TCATCTAGAAAACAG[A/G]TAGCTATCTCAAGCA | 9169 |
rs540473556 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932451 | GGGTTTCATAGTACA[C/T]ACATCTGGAATTCTT | 9169 |
rs540597206 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977541 | TCACAGAACTATACA[C/G]CTCAAAAAGCTCAAT | 9169 |
rs540625028 | snp | C/T | 1.64803e-05 | 0.00287052 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927427 | CGCAAGATCAGAAGA[C/T]GGCATATTATTTTCA | 9169 |
rs540625096 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966366 | TAGCTCCAAGATTTA[C/T]AGAATACTATAGGTA | 9169 |
rs540646663 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974590 | TCCCTAAGAAACAAC[C/T]CTTCATTCAAAATTT | 9169 |
rs540662258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985867 | ACATTGTTACACTCA[A/G]CAGAATTTTTTTTAG | 9169 |
rs540697391 | in-del | -/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979079 | CAAGTATTAGGTGGT[-/G]GGGCTTTTAGGAGGT | 9169 |
rs540759023 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930562 | AGACATTCACAACAC[C/T]TGAGTACACCAGAAT | 9169 |
rs540793856 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992848 | TATTTGTTTCCTAGC[A/C]GAGAATTAAGTTTTC | 9169 |
rs540886460 | snp | A/C | 0.000346081 | 0.0131499 | intron-variant, splice-donor-variant | SCAF11 | GRCh38.p7 | 12:45953827 | AGAAAAAATAACTTA[A/C]CTCTAAGGTTTTTAT | 9169 |
rs540935627 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950877 | GTGCTACCTAAAAAC[A/G]GTTTGTTTCTCCTAT | 9169 |
rs540949445 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961403 | AAGCACAGAGTCAAG[C/T]ACACTGAAAAATTAA | 9169 |
rs541010820 | in-del | -/G | 0.00795532 | 0.062565 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943556 | GGGTATGTACATATA[-/G]GAAAAAACAAAATAT | 9169 |
rs541014696 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981449 | TAATCTCTAAACAAA[C/T]AGCCCCTTACAGCTC | 9169 |
rs541017551 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932008 | ATGCAGACTTTAAGC[A/G]TACATTTGCTAACTT | 9169 |
rs541094021 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985151 | ATTTCAATGTCTATG[C/T]GTAGAAAACCATGAA | 9169 |
rs541128787 | in-del | -/AT | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926082 | ACTCATACAAATAAC[-/AT]ATTAAATTTATAATT | 9169 |
rs541160211 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943610 | AGTTTCAGGCATCTA[A/C]TTGGAACATATCCCC | 9169 |
rs541267483 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988102 | ACAAGGTGCAAGGTT[A/T]TTAACTTATTTTGGG | 9169 |
rs541306211 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930978 | ACCTATGTTGTTCAA[A/G]GGTCAACTGTATTAT | 9169 |
rs541367167 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958196 | AGGCGTGAGCCATCA[C/T]GCCTGGCCAATAAAT | 9169 |
rs541442229 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981272 | ATCAGTAAGACATGT[C/T]AATGAGAAAGGAAAC | 9169 |
rs541496652 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942485 | ATCACGTTACTCCTG[A/C]AAACACTCCCTAGCT | 9169 |
rs541503665 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989271 | AATGCATTTATTAAT[A/G]TGCTTTTCCCAAAAT | 9169 |
rs541528297 | snp | A/G | 1.6851e-05 | 0.00290263 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934468 | TATCTTTATTGCTGC[A/G]TTTTTCTTTCCTCCT | 9169 |
rs541631818 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919407 | GTTAATGGATAACTA[C/T]TATTAGTCTCAAAAT | 9169 |
rs541650432 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979915 | AATTCTGCCACATTA[C/G]CATAAGGCATGAATA | 9169 |
rs541689712 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955815 | TTTTAAAGTATCTAA[C/T]TCAGTTTCATAACCA | 9169 |
rs541755191 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977028 | CCAAAAAAGAAACCT[C/T]GAGGCCCACATAATT | 9169 |
rs541781102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965207 | AAAAAAGATAGATAC[A/G]CCAGCCAAGTATGGA | 9169 |
rs541791409 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981629 | ACTGTTCACCTATCT[C/T]TAACAAAAATTTAAA | 9169 |
rs541831128 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984263 | TATAGATTAGTTCTG[C/T]TGCAAAATGTCTTCC | 9169 |
rs541923420 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918994 | CTAACTCTAAGCTTG[C/T]TTTAGAGCTTGGGTA | 9169 |
rs542009790 | snp | A/C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920215 | TTACACTCATAACAA[A/C/T]AAAGCTTATGAACTA | 9169 |
rs542038496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987656 | CAGCGTAGGGGAAAG[A/G]AGATTGGAGAAAGGG | 9169 |
rs542067350 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940977 | ACTTGGCTAATTTTT[C/G]TATTTTTTGTAGAGG | 9169 |
rs542108241 | snp | C/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960299 | CAAAACATATACTCC[C/G]ATTAAGTTGTTGAAA | 9169 |
rs542129709 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956729 | TTTATTCTGACAATA[A/G]GCAACACTTTATCTA | 9169 |
rs542247545 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960548 | AGAGAGATTTACCAA[C/G]CATATTAATTCAGCA | 9169 |
rs542342925 | in-del | -/ATTT | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993058 | TGTTTGGATGTAAAG[-/ATTT]ATTATTCTCTCTGAT | 9169 |
rs542346896 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970032 | TCCTGAGTAGCTGGG[A/G]TTACAGGTGCCCGCC | 9169 |
rs542350524 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979759 | ATGTTACATAAATGT[A/G]TATGTATCAATGTGC | 9169 |
rs542365223 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923778 | ATCTCCGACTACCAG[C/G]TTCAAGTGATTCTTG | 9169 |
rs542411076 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932899 | TCCCTTTTAAATAAA[C/T]CTAGCATATACACAG | 9169 |
rs542421633 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978726 | ATTTTTACTTCAACA[A/C]TTGGTGTACCCTGGA | 9169 |
rs542428300 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923491 | AACAAATATTAAAGT[C/G]CCCTCACTTTAAAGC | 9169 |
rs542700311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968716 | GAGGCTGAGGCAGGC[A/G]GACCACTTGAAGTCA | 9169 |
rs542783402 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958836 | TTTTGTTTAAATAAC[C/T]ACAGAACCAAAATTT | 9169 |
rs542804877 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966998 | ATATTATCCCTTTAT[A/G]TAACGCAATGATTTA | 9169 |
rs542824828 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975138 | ATGCTGTAAACGGAT[A/G]TGCTGTCATCCAAGC | 9169 |
rs542855655 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937580 | TGTGTTTCACTGTAG[C/G]GTGATCAAGCAGACA | 9169 |
rs542874937 | in-del | -/CAC | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922852 | ATAAGAAATTCCCTT[-/CAC]CACTCATACAATAAA | 9169 |
rs542929873 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973969 | GTTTGGCATTAAAGC[A/T]AATATTTATAACACT | 9169 |
rs542940964 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934723 | AAAGGCCACAATACA[A/G]AAACTGGGTGAAGTA | 9169 |
rs542980380 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944826 | GAAGTAAGGCTAGAG[G/T]CCAAACTACAACTTC | 9169 |
rs543032985 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967899 | GGACTCCAGTTTTCA[A/T]TCCAAGGATCCACAA | 9169 |
rs543045572 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944021 | TTCACCTTCTAAAAA[C/T]GAGCCCAGGCAAGAG | 9169 |
rs543188596 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975611 | CACTGGCTTGAAGAG[C/T]GTTAGAGACGCGCTC | 9169 |
rs543323257 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943648 | AAGGGGTAACTACCA[C/T]ACCCAGTTCCCTTCA | 9169 |
rs543404255 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973240 | AACTTGAAGATAAAC[C/G]ACTAGAAATTACCCA | 9169 |
rs543424475 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975649 | GGCTTTGAGTTAAGA[A/G]AATGTTACGACTGGT | 9169 |
rs543468600 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930880 | TATGCGATTTTTCTG[C/T]TTTTTCAGTGTTGCA | 9169 |
rs543471739 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980523 | TATTGTGGAAACACC[C/T]AGCAAGTGATGGAGC | 9169 |
rs543541060 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939647 | AGGTTGCAGTGAGCC[A/G]AGATCGTGCCATTGA | 9169 |
rs543549046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936343 | GATGGGGTTTCACCA[C/T]ATTGGTGAGGCTGGT | 9169 |
rs543573745 | snp | C/T | 0.00716266 | 0.059414 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990635 | TGCGCGTCTCCCTCC[C/T]CCTCCCTTCCCTCGC | 9169 |
rs543613727 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982379 | AGCCATCTAGGCATA[C/T]AAAATAGTGCTATAC | 9169 |
rs543641329 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973912 | CAGTAAATGCCTGAG[C/G]AAACATAGTTAACTA | 9169 |
rs543656532 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981250 | TTGTTCGACACCATA[A/G]AAGTATATCAGTAAG | 9169 |
rs543677783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942693 | CTTCATGGCTTAACT[C/T]CTTACTTCTTGAAGG | 9169 |
rs543716662 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989123 | ACAGACTTGATTACA[C/T]GTCAAAATTTTAATA | 9169 |
rs543891991 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969595 | CTTATTGTCAGAAAC[A/T]ACAGAGAAATAGGAA | 9169 |
rs543895364 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958264 | AGATTATCTTGTCTG[C/T]AGGAAATCATAATTG | 9169 |
rs543912656 | snp | A/C | 1.64735e-05 | 0.00286993 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922978 | GGCTTCCACTGCAAC[A/C]CTTACTTTGCTTTCT | 9169 |
rs543991788 | in-del | -/ACTG | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955779 | TCACTTGTTTGAATT[-/ACTG]ACTTTCATTTCAATA | 9169 |
rs544039496 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973007 | AGATATATAGATATA[G/T]ATATAGATATATAGA | 9169 |
rs544170480 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984999 | CACACCCAGCCACTT[C/G]CTTACTTTTGGACAT | 9169 |
rs544184226 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933747 | GCTCAACTAACTGTA[C/T]GTGATTTTAAAACCT | 9169 |
rs544224599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947803 | TGCCTCAACTTCCTA[A/C]GTAGCTGGAACTGCA | 9169 |
rs544226683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955339 | TTTTTTGTAGAGATC[A/G]GGTTTTGCCATGTTG | 9169 |
rs544269339 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950866 | AAAGACTAACAGTGC[C/T]ACCTAAAAACGGTTT | 9169 |
rs544270633 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946804 | CCAAAGCTGATAAGT[A/G]TTTTTCAGAAATAAT | 9169 |
rs544286516 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954851 | TCAGCCTCCCAAAGT[A/G]TTGGGATTACAGGAG | 9169 |
rs544374022 | snp | C/T | 0.000184145 | 0.00959368 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991869 | GACTAAGCTCTGCTC[C/T]CCGCGCGCGGCTCAC | 9169 |
rs544378527 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970045 | GGATTACAGGTGCCC[A/G]CCACCACGCCCAGCT | 9169 |
rs544400822 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953168 | CCTACTTTTAAGTAC[G/T]ATGGATTTAGGAGGC | 9169 |
rs544483806 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920056 | GAAACACTGTCTTAA[C/T]ACTTTATTAGAAGAA | 9169 |
rs544550543 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938410 | AGTAGAATCACTTGA[A/G]CCTGGGAGGCGGAGG | 9169 |
rs544575411 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934910 | CATCTAGAAAACAGG[A/T]AGCTATCTCAAGCAG | 9169 |
rs544625757 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992367 | TTAAAATGCTTTCTT[A/C]TGATGGAACAACAAA | 9169 |
rs544640626 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931015 | CATCACGTTTCACAA[C/T]TGATCTTTAGAACTT | 9169 |
rs544760912 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931124 | CTAGTTCTACGAGAT[A/C]AACTTTTTTAGATTC | 9169 |
rs544823253 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932118 | CCCCTAGAAAGTGTC[C/G]TCACACTCCTTTGTA | 9169 |
rs544838661 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930140 | TATATCATTTGTTTA[C/T]AAGATGAATCATCTG | 9169 |
rs544914434 | snp | A/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983997 | CTAAAAGTGTTGGTA[A/T]AATAATCTTTTACAA | 9169 |
rs544914594 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992269 | TTTGGAGTTTTTCAG[C/T]GTACTGTTTTTGATA | 9169 |
rs544921772 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976157 | GGGGAAAGGTAAAGG[C/G]ACATACATGGTGGTA | 9169 |
rs544975784 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991364 | GAGCTCAGCAGTTCG[A/C]GACCAGCTTGAGCGA | 9169 |
rs545087080 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938476 | CCTGGGTGACAAGAG[C/T]GAGACTGCATCTCAA | 9169 |
rs545093364 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921615 | TACATTATTTAACTT[C/T]CTATAATTAGAGGGA | 9169 |
rs545139594 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944924 | CCACAAGGTATTTAA[A/T]CTCATCTCCCCCAAG | 9169 |
rs545200536 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952110 | TTTTAATATTCTATG[A/T]CTTAATATTTTCCCC | 9169 |
rs545365514 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988233 | AGGGCTTGCTAAAGG[A/G]AAGTTACAATGAAAA | 9169 |
rs545462809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950042 | TCATACATACATACA[C/T]ACATACATACTTACA | 9169 |
rs545520972 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964007 | TTTAAGAACAACAAT[A/G]ACAAAAAACTCCTGT | 9169 |
rs545527191 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957327 | GAATGGACAAATTTC[C/T]ACCTACTGCATAAAG | 9169 |
rs545577811 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952890 | CTATGTAAAAAATGT[G/T]ATCTTTGCCTTTCTG | 9169 |
rs545590425 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956635 | ATTAACCCCCAGTAA[C/G]AACACATTTCATCAA | 9169 |
rs545590544 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984757 | TGGAGTGCAGTGTGG[C/T]GATCTTGGCCCACTG | 9169 |
rs545604715 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978432 | GGTACTTTTAAGGGA[G/T]GAGTTATACATTTGG | 9169 |
rs545651818 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964561 | AGTCCCAGCTGCTCG[A/G]GAGGTTGAGGCAGGA | 9169 |
rs545699772 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974999 | GGCAACATTTATCTC[C/T]GTGTATTTCCATCAG | 9169 |
rs545746693 | snp | A/G | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45919079 | TTTGTAAGGGATTAT[A/G]ATTGAAAAGTCACCA | 9169 |
rs545793851 | snp | C/G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920013 | AGTTCTAATCTAAAA[C/G/T]AACTAAGGAGGTGTG | 9169 |
rs545802544 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971977 | ACTGTCCCAGGGATC[G/T]AGAAAATACCATGGA | 9169 |
rs545853367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941146 | TATATCAACACAAAC[C/T]GTTCACCATTAAAAT | 9169 |
rs545964291 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921022 | AGATTTGCTCCTGTT[C/G]CCCAGGCTGGAGTGC | 9169 |
rs546057221 | in-del | -/TAGAT | 0.00478085 | 0.0486577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984250 | ACTCCTTAAAGCTTA[-/TAGAT]TAGTTCTGTTGCAAA | 9169 |
rs546087058 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948144 | CACTATGTTCCCCAG[G/T]CTGGTACCAAACTCC | 9169 |
rs546136987 | in-del | -/A | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973093 | AACAAATGGAAAGCC[-/A]AAAGATCACAGCAAA | 9169 |
rs546221220 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993311 | ATATCAGTCCTGTCA[C/T]ATAGCAACAGAAACC | 9169 |
rs546242282 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986934 | CCTCTTTTTCTTCCC[A/C]GTCTCAGGTATGTCA | 9169 |
rs546287967 | in-del | -/A | 0.279991 | 0.248195 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979889 | TGCAAACTTAAAATT[-/A]AAAAAAAAAAAATTC | 9169 |
rs546288331 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993904 | ATAAGAGGACATTTT[C/T]ATTTTAATGATCTCT | 9169 |
rs546303127 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930012 | TATATTTTTTATGTT[A/T]TGTGTTACATACTGT | 9169 |
rs546329556 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986697 | CCACGTGTTGTGGGA[A/G]CAACCTGTTGGGAGA | 9169 |
rs546396233 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951351 | ATTCTAAAATGTTAA[A/G]TATTTTATAATTAAG | 9169 |
rs546407632 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947838 | TGTGTCACCATGCCC[A/G]GCTAATCTGTAAATT | 9169 |
rs546444737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947710 | GAGACAGAGTCTTGC[C/T]CTGTTGCTCAGGCTG | 9169 |
rs546445553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963105 | GACAGAAAAGGAAAT[A/G]TAAGACATAGCCTGT | 9169 |
rs546454266 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993710 | CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG | 9169 |
rs546517550 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975408 | AAAATCTTTTGTTTA[A/G]TATAGCCACTTTCAT | 9169 |
rs546536829 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923277 | TACTAAAGAAAAATG[C/T]ATATTTCAGGTAATT | 9169 |
rs546539217 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977912 | CTAAATTCTAAGGCA[C/G]AGTTGCAGAAACAGA | 9169 |
rs546548315 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954722 | ATACATGCATGTATC[A/C]CCGTGCCTAGCTTTT | 9169 |
rs546556177 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968874 | GAGGTTGCAGAGAGC[C/T]GAGATCATGCCATGG | 9169 |
rs546580634 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932345 | TAACAAAAGACTATC[C/T]GATTCAATATAAGGT | 9169 |
rs546612078 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925874 | AATCCTGCATAGGAA[C/T]ATCCCAAACTCTTCT | 9169 |
rs546621752 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940576 | AGCCTTTTAAAAAAG[A/G]CTTTACAAAATGATG | 9169 |
rs546623102 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933323 | ATAGCAGTCGTTTTT[A/G]TACCTGGCATTATGA | 9169 |
rs546658829 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961090 | TTCACTGTCTATGAC[A/G]GTAATATCTCTAATT | 9169 |
rs546668188 | in-del | -/TTTCA | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935943 | GGCAGTGATACGCCT[-/TTTCA]TTTAATTTTTATCAA | 9169 |
rs546679013 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988329 | CAACTATCTCTGATA[C/T]ACTTTAAAAGTTCAG | 9169 |
rs546765028 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947375 | TGTTAAAATAGGCAA[C/T]GGTTTTAACAGCAAC | 9169 |
rs546792343 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938089 | TTTCTGCTAAGACAA[C/T]TTACCATCCCCCTCA | 9169 |
rs546855552 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946076 | GAGGTAAGCAGATAT[C/T]GTCTTTTTTAAAAGG | 9169 |
rs546904231 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983380 | CAAACCTGGAGTTCA[C/G]AACTATGGGTAGAGT | 9169 |
rs546915251 | snp | A/G | 1.6684e-05 | 0.00288821 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945222 | AACAAAAAAAAAGGT[A/G]GAATCCACAAGCAAA | 9169 |
rs546965689 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990989 | GAGGACAATGAAAGA[A/G]GCTTTAAGGGAACTG | 9169 |
rs547010601 | snp | C/G/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921068 | GCTCACTGCAATCCC[C/G/T]GCCTCCCGGGTTCAA | 9169 |
rs547184564 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973313 | AGGCTTAGGGACCTG[G/T]GAGGCAGTACCAAAA | 9169 |
rs547193012 | snp | C/T | 8.24504e-05 | 0.00642016 | missense | SCAF11 | GRCh38.p7 | 12:45926379 | CACTCCCTGAACTGT[C/T]TGAATTCCCTGAGAG | 9169 |
rs547240798 | snp | A/G | 0.000973868 | 0.0220451 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991954 | CCGTTCTGTTCGCGC[A/G]TGCTGCGCTCTCCAG | 9169 |
rs547255628 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942021 | TCAATGAACAGTAAA[C/T]GTATTTTCTCATCCT | 9169 |
rs547334717 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965320 | GGAATTAAAAGGCTG[C/T]AGAAATTCTGAGATT | 9169 |
rs547366606 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982394 | CAAAATAGTGCTATA[C/T]GTATATTTACATTAA | 9169 |
rs547428097 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978240 | TCTAATAACCCCACC[C/T]CTGCTTAAGTTATGG | 9169 |
rs547452110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949086 | TAAAGCAAGTGAATG[C/T]GATGATCAAATTTGT | 9169 |
rs547530673 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929261 | CTCCCAGGCTCAAGC[A/G]ATCCTCCCACCTCAG | 9169 |
rs547636192 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936895 | AGAATTGTCTAGGTT[A/G]GTAATTATTTTCCCT | 9169 |
rs547681309 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973852 | CTTAAATGAAGTTGT[C/G]TCAGAAGAAAAACAA | 9169 |
rs547698500 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950202 | AAAATAAGATAATAG[A/G]GGTAAATGTTCTATG | 9169 |
rs547713341 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987963 | CATACATTAAGTTCA[C/T]AGACACAACTTAAAA | 9169 |
rs547763059 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973239 | AAACTTGAAGATAAA[C/G]CACTAGAAATTACCC | 9169 |
rs547775771 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979057 | ATGGCACCTGTTACT[A/G]CATCTTCAAGTATTA | 9169 |
rs547824803 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980711 | TTTATCTGAGTCCAG[C/T]GGTAATAAATAGCAG | 9169 |
rs547824887 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972450 | AGTAGCCAAGCATAG[A/T]GGTGTGTCACTGTAG | 9169 |
rs547847510 | in-del | -/AG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922797 | GACATCAACACATCT[-/AG]AGAGAATCCTTCAAA | 9169 |
rs547886290 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956108 | AACCTTCCTTATTTG[G/T]GAATTCAGGATCCTC | 9169 |
rs547980984 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941248 | TCGTAGACACCTTAC[G/T]TATCGAAAAACGAAT | 9169 |
rs547989588 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964300 | TAAAAGAACACAGTA[C/T]GAGCCAAGCCAGTTT | 9169 |
rs548018637 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933722 | CACACAATCGTATTC[C/T]GTGCTGCTGGCTCAA | 9169 |
rs548041849 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949302 | AAATTGGAATGTGCC[A/G]CAAGTATAAAATAGA | 9169 |
rs548042948 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936508 | TCCTTTTCTTCCTTA[-/T]TATCCATCATTAATT | 9169 |
rs548043943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940819 | CTTTTATTTATTCTT[C/T]TGAGAAAGGGTCTTA | 9169 |
rs548050557 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971333 | AGTGAGATCAAGGAG[C/T]TCCAGTTCCAGGTAA | 9169 |
rs548112714 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970673 | CTAGGAATCTTTCAT[A/G]TTCACTTCCTCCACT | 9169 |
rs548144248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965045 | AAAATCACAGTGAGA[A/G]GTAATAAGAAATAAG | 9169 |
rs548186937 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935166 | CTCACAAAGGGCCTA[C/T]TGACATTGTTCAAAA | 9169 |
rs548188727 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949244 | CCAAGACAACAGTCA[C/T]TAGCCACATATGGCC | 9169 |
rs548200660 | snp | G/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918660 | TGCAGTGAGCTGAGA[G/T]GGCGCCACTGCATTC | 9169 |
rs548345108 | snp | C/T | 0.000310862 | 0.0124633 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964146 | CTCCCATATTTAGGG[C/T]ACATACAGTTTTCTT | 9169 |
rs548401448 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940872 | CAGTGGCATGATCAT[A/G]ACTCACCTGCAGCCT | 9169 |
rs548498255 | in-del | -/C | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973602 | GAAAAAACAATGATG[-/C]CATTACTTACGAGGG | 9169 |
rs548575425 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982534 | CAACATGGTGAAACC[A/G]TTTCTACTAAAAATA | 9169 |
rs548577826 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964869 | AGTATGGAGAAATAC[A/G]ATAACATTTAGCTAG | 9169 |
rs548594176 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922348 | AAAGGCAAAAAAGTA[A/G]ACAGGAATTAGTAGG | 9169 |
rs548606096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986192 | TTACAGCCAATACTC[G/T]TCCTCTGAATTTCAG | 9169 |
rs548617122 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955166 | CAGACTCAGCCATCA[C/T]AATTTTTTTTTTAAA | 9169 |
rs548677925 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963336 | AAAGACGAAACCAAG[A/C]CCTTAAAAGCAGAAA | 9169 |
rs548759061 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951908 | CTCCTGTATGCTAGA[C/T]AGTTGGAATACAATG | 9169 |
rs548822750 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959341 | TTAAAAAGATTTTAA[C/T]GTCAGGCTATCCCTT | 9169 |
rs548840261 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977774 | AGCTTGGGAGGGGGT[A/G]TTTGAATGTTTTATC | 9169 |
rs548846506 | in-del | -/ATT | 0.000181325 | 0.00951996 | cds-indel | SCAF11 | GRCh38.p7 | 12:45928192 | TTCCAAACACAAAAC[-/ATT]AGCCTCTATACCTGT | 9169 |
rs548886967 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970190 | TGAGCCACCGCGCCC[A/G]GCCTCAACTAATTTT | 9169 |
rs548926481 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930567 | TTCACAACACTTGAG[A/T]ACACCAGAATAGCAA | 9169 |
rs548947951 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989505 | CAAAATTCAACATTT[A/G]AATCCGTGAATGTCT | 9169 |
rs549117513 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967975 | CACAGTAATACCACA[C/T]AGAGTCATAGTCCTA | 9169 |
rs549136701 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989830 | CGGCGTAGTAAAGTT[C/T]GGTTTCACTAGCGGG | 9169 |
rs549174611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967414 | TTTGGGAGGCTGAGG[C/T]GGGAGGAGCGTCTGA | 9169 |
rs549202018 | in-del | -/CATA | 0.0279526 | 0.114869 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950027 | AGTAAAACAATCATT[-/CATA]CATACATACATACAT | 9169 |
rs549237985 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974711 | GTTACTTCCTCCACA[C/G]AAGTTTTGAATCCCT | 9169 |
rs549273867 | snp | C/T | 1.66827e-05 | 0.00288809 | missense | SCAF11 | GRCh38.p7 | 12:45933201 | TCTGCCTAATCAATG[C/T]ACTGATTTCACTGGC | 9169 |
rs549339028 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924610 | AAGGTTTACCATAAC[A/T]GAAATCAAATAAACA | 9169 |
rs549413882 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958471 | TTCATCAGTTCAAAT[A/G]TCTTTGATTAATTTT | 9169 |
rs549456353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932629 | GCTTGATTTAAGTAT[A/G]TATTATTTATCTAGC | 9169 |
rs549462108 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942890 | TCCCATTGACAAGCA[C/T]TTTGTTGTTTTTGTT | 9169 |
rs549510500 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936333 | TTTTAGTAGAGATGG[G/T]GTTTCACCATATTGG | 9169 |
rs549514662 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968742 | AGTCAGGAGGTTGAG[A/G]CTAGCCTGACCAACA | 9169 |
rs549520786 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970186 | GGCATGAGCCACCGC[A/G]CCCGGCCTCAACTAA | 9169 |
rs549525046 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951040 | TACTCAACTCAGACA[C/T]GTTTTTTTGTTTTTT | 9169 |
rs549525480 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942344 | TGTGGCCTAGAAAAA[C/T]GTCACCTAAAATAAA | 9169 |
rs549544365 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958382 | ATATATTGTTTTTGC[C/G]CACAATATGGGTAAA | 9169 |
rs549640148 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925400 | TCTACTAAAAAAATA[C/T]AAAAATTAGCCAGGC | 9169 |
rs549793495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967291 | TAAGACCCATATAGT[A/G]AAATATACATGAGAA | 9169 |
rs549799059 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929028 | GAGTAATATGACTTA[C/T]TCATCAACTTTCTTA | 9169 |
rs549832563 | in-del | -/TTCTT | 0.00199481 | 0.0315187 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918892 | TCCTTTTTCAGTCTC[-/TTCTT]TTACACATTTACTAA | 9169 |
rs549862374 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925644 | AGAAACTGACTAGTT[-/A]AAAAAAAAAAATCAC | 9169 |
rs549903508 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942276 | GTACATACAGAATGG[A/T]ACCACTTATCATCAT | 9169 |
rs549972819 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977125 | AAATGGAAGATGAAC[A/G]CTTCCCAAATCATTT | 9169 |
rs550032671 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981547 | TATAATCCGTCATCC[C/T]TGAATAAATACGTTT | 9169 |
rs550082594 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942834 | TAAAGCATTTATTAC[C/T]GCCTGTTTTATATTT | 9169 |
rs550153006 | snp | C/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921134 | ATTACAGGCGCCCAC[C/G]ACCACGCCTGGCTAA | 9169 |
rs550212791 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972196 | TAATGTAAAGTTTTG[A/G]AAACAGAACTGAAGT | 9169 |
rs550232174 | snp | A/G | 0.00676609 | 0.0577691 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993982 | CTGAGCAACATAGTG[A/G]GACCTAGTTTCTACT | 9169 |
rs550274010 | snp | A/G | 0.00159617 | 0.0282053 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993809 | GAAAAAGAAAAAAAA[A/G]AAAAACATGGTTCTA | 9169 |
rs550340161 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964716 | ACTATTAAGCAACAA[A/C]GCCTAAATGATATAT | 9169 |
rs550382485 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920598 | TGAGATATTCTAGTA[C/T]TAAAAAGAGAAAAAA | 9169 |
rs550487971 | snp | A/G | 1.65985e-05 | 0.00288079 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961752 | TGATTACAGCTTTCT[A/G]GAAAACCAACTTCCT | 9169 |
rs550517466 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985194 | TCTCCAATTTCAGTC[C/T]GCAAGATTTGTTCTT | 9169 |
rs550532406 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976256 | TTCTTAGAGCTACCA[C/T]TAAAAACATTAGTCA | 9169 |
rs550548533 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939293 | GAATTCGCAACTTCA[C/T]AAACTCTATTCATTA | 9169 |
rs550549884 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924404 | CAGTGCAAAACAGGG[C/G]AAAAATGTAAAGCAC | 9169 |
rs550591520 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925922 | TGAAAATATTTAAGT[C/G]TTTGGCAAGGTTTGG | 9169 |
rs550623661 | snp | A/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993801 | AAAAAAAAGAAAAAG[A/T]AAAAAAAGAAAAACA | 9169 |
rs550658573 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947239 | AGCTTAAGTTTCAAA[A/T]GTATTAGAACAAGTT | 9169 |
rs550665504 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983259 | AGATGGAAAGTACGA[G/T]AAACTAGTTAGGAGA | 9169 |
rs550677667 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968420 | TAACATATTGTTTCT[A/G]CTAGATACTGAAAGT | 9169 |
rs550717542 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954275 | CTTGCTCTGTCCCCC[A/T]GGCTGGAGTGCAGTG | 9169 |
rs550719311 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946287 | AAGGGAGAGGCAAAA[C/T]TGAATGAAGTTTGTC | 9169 |
rs550780763 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953551 | CCCATCTCTGAAACA[C/T]AGATAAATAAAATTA | 9169 |
rs550816313 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949766 | ATTTTGTTGGTATTC[C/T]AGATAGAGATGCACA | 9169 |
rs550887851 | snp | C/T | 9.95421e-05 | 0.00705416 | missense | SCAF11 | GRCh38.p7 | 12:45951702 | GCCTGAAAAGGTTTA[C/T]GGTCAATAGGACATG | 9169 |
rs550924209 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990510 | CTGGCTCGGTCCGGA[A/G]GCGGCGGCGAAGCAG | 9169 |
rs551025164 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964207 | TAAGATAAATTATAA[C/T]AGAGAATTTTATGTT | 9169 |
rs551055814 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930375 | CTTTTTACTGTGATA[C/T]GCAATCTATTAGAAA | 9169 |
rs551071302 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959216 | GAAGTTGCAGTGAGC[C/G/T]GAGATGGTTCCACTG | 9169 |
rs551119016 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922244 | ATGCTTAAAGGGATT[A/T]AAGCCAAAATAGAAA | 9169 |
rs551181161 | snp | G/T | 6.74059e-05 | 0.00580503 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923191 | AGTTAATGAATTACT[G/T]GTACTCGATAGAAGT | 9169 |
rs551193650 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924187 | AAAATTATAAGCAAC[A/G]AATTGTTTGCAAATT | 9169 |
rs551206370 | in-del | -/A | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944115 | GGCCAAATTACCTAG[-/A]AAAAAATCTGTAACA | 9169 |
rs551272053 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968762 | CCTGACCAACACGGT[A/G]AAACCCCGTCGCTAC | 9169 |
rs551299126 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931935 | TTTTCCAGCTTTCAT[C/T]ATGTTCTTCACTACT | 9169 |
rs551307516 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973643 | TAATGATTTGAATCA[A/C]CGGTGATTTCTTATC | 9169 |
rs551334245 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983189 | GTGGTTTATAAGATG[C/T]TTAAATTGGGGATTT | 9169 |
rs551355188 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991987 | ACCCTGACGCCTGCC[C/G]GGGATGAGTTTCCTC | 9169 |
rs551397462 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990797 | AGACCGAGAAGCGTG[A/G]TGGGTGGAGTCACGT | 9169 |
rs551459123 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990267 | TCGCCCTAGGCCCGC[C/T]CCAGCGCTCTGCGCC | 9169 |
rs551461827 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974800 | TCCTTCTATGAATTA[C/T]GAATGTTCTTTATGG | 9169 |
rs551519299 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982766 | CCCAGAGAATTTTTA[G/T]AACAGTGTTGTTTTG | 9169 |
rs551522137 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960763 | CCTTTCCACACTATT[A/C]ATGAAAATTTAAGCA | 9169 |
rs551559546 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966933 | GTGATAAAATGTCAT[C/T]TGAAAGTTAACACAG | 9169 |
rs551650857 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968189 | TATCTATAAGTCAAA[C/T]TGTATTTTCTTTTAT | 9169 |
rs551672552 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932246 | AGTGTCCCTAGAGAC[C/T]TGTTAAGACCCCCTC | 9169 |
rs551673610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958419 | AACTTCCTAACTGAA[C/T]AGATGATAAGCTTTA | 9169 |
rs551725231 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979998 | CATAACCTAGATTTT[G/T]GTGTAAGCGTTTCAT | 9169 |
rs551742508 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951071 | CAGGTAAGCAAAAAA[C/T]TAACATAAATACAAA | 9169 |
rs551786575 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979300 | TGGAGAGGGCATAAA[A/C]ATTGAAACCACAGAA | 9169 |
rs551788521 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987867 | CACAGTGACTTTTTA[A/G]GAAGATATTTTTGAA | 9169 |
rs551804307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936446 | CACGCCCAGCCAGCT[A/T]CATTCAGGTATTTTC | 9169 |
rs551819082 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925971 | AATATACTTATGTAG[A/G]TAAACGTACGTGTAT | 9169 |
rs551851863 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987228 | TGGGAGACAGCGAGA[C/T]GCTATCTGAAAGCAA | 9169 |
rs551867562 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935952 | ACGCCTTTTCATTTA[A/G]TTTTTATCAAAGTAA | 9169 |
rs551881337 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944231 | TACAGCAATGACATA[A/G]AAAAGCAAAGACTGT | 9169 |
rs552089323 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945423 | TATCATGCACTGATT[C/T]TGGTAACTATGCTGA | 9169 |
rs552096968 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933076 | ACTTAAGTACTAATG[C/T]TATCTTGTTCATGTT | 9169 |
rs552121032 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971598 | AACAACAGAGAGCAA[A/G]CTCTAAGAGAATCCC | 9169 |
rs552198109 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962130 | TTAAGAGCAAATTTC[C/T]CATTCAAATTTATCC | 9169 |
rs552206182 | in-del | -/TAATT | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979797 | TGAATATTTTACACA[-/TAATT]TAAAGAAGCATTTCA | 9169 |
rs552328859 | in-del | -/A | 0.207559 | 0.246371 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929098 | GGCAATTTTATAGAG[-/A]AAAAAAAAAAAGGAA | 9169 |
rs552344451 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939881 | ATGGTTTCTGTTCAG[C/T]GTAACTGGGTAAATA | 9169 |
rs552348299 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948652 | TCCAATTAAAAAGTG[C/T]AGTCCAAATACATAT | 9169 |
rs552368893 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993917 | TTTATTTTAATGATC[C/T]CTGGCATTTTTATGG | 9169 |
rs552402151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977720 | TTCTTATAACTACTG[C/T]CAACACAGAAGGCAC | 9169 |
rs552496780 | snp | C/T | 0.00038956 | 0.0139509 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991862 | CCCGCAGGACTAAGC[C/T]CTGCTCCCCGCGCGC | 9169 |
rs552532280 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920862 | TCTTGTAATTCTTAG[C/T]CCCAAGGAAGGGAGG | 9169 |
rs552563970 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939132 | AGTTTATATAATTTT[A/T]CTAAAGTCACAGGTG | 9169 |
rs552627057 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947164 | AATTATGAATCTGAC[A/G]ACATATTGACTTAAA | 9169 |
rs552652608 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969775 | ACAGTCTTGCTCTGT[C/T]GTCCAGGCTGGAGCG | 9169 |
rs552660292 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955158 | CTTTGACACAGACTC[A/G]GCCATCATAATTTTT | 9169 |
rs552729298 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977340 | ATTTTGTGAAAGAAG[A/C]CAGTCTCAAAAGGCA | 9169 |
rs552792387 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985297 | ATTTGATCAACCCCC[C/T]GCATGTGGCCAGTTT | 9169 |
rs552855092 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932011 | CAGACTTTAAGCGTA[C/T]ATTTGCTAACTTTTT | 9169 |
rs552918820 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932799 | TGATTCAGCGGACAG[C/G]ACGCAGGTAAGACTG | 9169 |
rs553011219 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953637 | ATTCCTATTTTAAAG[A/G]TAAATTTAGAGAAAC | 9169 |
rs553051858 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968548 | ATTTAAAAAAAAAAG[C/T]ACTGATAAAAATCAG | 9169 |
rs553075088 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987015 | TTAGCTCCTTCTATA[C/T]TAAGACAAATGATAG | 9169 |
rs553075356 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950276 | ATTCAAGAAGTTCAA[C/T]TGCAAAGGGAAAAAG | 9169 |
rs553178581 | snp | C/T | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927895 | CTCTATAAGCTCCTC[C/T]GTTTTTAGTGTAAAA | 9169 |
rs553257250 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946515 | CAAATCTCAGAAAAA[C/G]CAGTTAAATATGGGG | 9169 |
rs553278782 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936153 | GTTTTTTTTGTTTTT[G/T]TTTTTTGAAACAGAA | 9169 |
rs553302449 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923745 | TGGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG | 9169 |
rs553322503 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945625 | TACTGCAGTCTTGAC[C/G]TCCTGGGCAGAAGCA | 9169 |
rs553374155 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45960155 | AATTCCACCTCTAGA[C/T]ACATACCCTAGAGAA | 9169 |
rs553397312 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957250 | TTGAGGAAAAATTGA[C/T]TGAAAATTCCAGATA | 9169 |
rs553429162 | snp | C/T | 1.83051e-05 | 0.00302527 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924702 | CAATGGCTATATTGA[C/T]TAAACTTGAGTTGCT | 9169 |
rs553433094 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45928982 | ATACTTATAAATAAA[A/G]CTATTAATAAATGCA | 9169 |
rs553458504 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965115 | ATCGCTAATGATTGA[C/T]TGAGAACCTTAGATT | 9169 |
rs553521646 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964499 | GGTGAAACCCTGTCT[C/G]TACTAAAAACACAAA | 9169 |
rs553619376 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982881 | ATTGGAATATAAAGA[C/T]GGATTAAGATACTGT | 9169 |
rs553628344 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977301 | ATTTCATTCAACAAA[C/T]TGTATGCATCTTAAA | 9169 |
rs553666864 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933444 | TCAGAGTTGTATTTA[C/T]ATGATTGTTAAAAAT | 9169 |
rs553720236 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971937 | AGTAAATGAAAACCA[A/G]TTTTCTGGCCAAAAG | 9169 |
rs553742896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940879 | ATGATCATGACTCAC[C/T]TGCAGCCTCAACTTC | 9169 |
rs553781488 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979611 | AAGTAGTTATTATAA[A/T]ACCAAGACAGAAAAA | 9169 |
rs553806318 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940124 | TACTGTCTAAGAAAC[C/T]TCATAAGAAATGTGA | 9169 |
rs553829484 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919987 | TTCAATGTTCACAAA[A/T]TTGTTTCTAGAGTTC | 9169 |
rs553904706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972638 | CAAAAACATCAACAT[C/T]TTCCATAGCATTTAA | 9169 |
rs553975788 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930184 | GCAACTGCAGCTATA[A/G]ATCTCAATCTGTTCC | 9169 |
rs553991053 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948135 | GACGGTCCTCACTAT[G/T]TTCCCCAGGCTGGTA | 9169 |
rs553998183 | snp | A/C | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974667 | AATTCTATAATAGTT[A/C]TCCTGCTGTTTATAC | 9169 |
rs554050659 | in-del | -/TC | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968197 | AGTCAAATTGTATTT[-/TC]TTTTATTGGTTCTAC | 9169 |
rs554052137 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955226 | GTGCAGCGGCATCAC[A/G]GCTCACTGCAACCTC | 9169 |
rs554105742 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930653 | ACACAGCTATGATTT[A/G]ATACTGTATCTTTAC | 9169 |
rs554160177 | snp | A/T | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986616 | AACAATAAGATAGTT[A/T]TACTGCTTGATATGG | 9169 |
rs554165285 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922708 | ATTAACGTGACAAAT[A/G]TAAAACAGTTTATTT | 9169 |
rs554245178 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971745 | CTCTGTTCCTCATGT[A/C]CCAATTCCCAAATGA | 9169 |
rs554306231 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964438 | TTTGGGAGGCCGAGG[A/C]GGGCGGATCACAAGT | 9169 |
rs554369903 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978256 | CTGCTTAAGTTATGG[A/T]GGACAGAACACAAAG | 9169 |
rs554446864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963422 | CTCCAGACAGCAAGG[A/G]AAAAAAAATGAGTAA | 9169 |
rs554557430 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986525 | TCTCCTCCCTTTCAA[A/T]ACACATCACCACAAT | 9169 |
rs554658438 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954642 | TCACCTGATCACAGC[A/T]TACTGCAGGCTTGAA | 9169 |
rs554717776 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953787 | ACAGTCTCTCTGTGC[C/T]TCAGTAACCTTATTT | 9169 |
rs554817540 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946202 | AGAAACAAAATACCA[C/T]TGCAATGCCTTCTTT | 9169 |
rs554841161 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962386 | ATAAAAATTTAGTTA[C/T]TTCACATTTTTAAAA | 9169 |
rs554846980 | in-del | -/TATT | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930854 | CTTAATTTTTTTCAC[-/TATT]TATAGGTTATGCGAT | 9169 |
rs554847071 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926003 | TATATTTATATAATG[C/T]TAAGTGACTTGTAAA | 9169 |
rs554900693 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985664 | ATGAAAATGTATGTA[A/C]AATGTCTACAACAGA | 9169 |
rs554906897 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921466 | AGTGTCTCAATGTTT[C/T]GAACACTAAATTTTA | 9169 |
rs554912568 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975180 | ATTTATAGAGCACAG[A/G]GTAGATTCAGTATAA | 9169 |
rs554932390 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944446 | ACAACTTGGTATTCA[C/T]AGTGCATAAAAAATG | 9169 |
rs554937736 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939566 | AGCTGGGCATGGTGG[C/T]GCATGCCTGTAATCC | 9169 |
rs554962498 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993495 | AACATGGTTCTGGCC[A/G]GGCATGGTGGCTCAT | 9169 |
rs554996781 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943415 | GAAGAGTAAGTACAA[C/T]AAGAAATTTTGAGAG | 9169 |
rs555012791 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940992 | GTATTTTTTGTAGAG[A/G]TGGGTTTCGCCACGT | 9169 |
rs555024684 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982115 | TTTAATTATATCTAG[C/T]TCTGTGGCAGTTTTG | 9169 |
rs555094426 | snp | C/G | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989985 | CCCCTTCCCCCCCCC[C/G]CGTAGGACCCTGCAC | 9169 |
rs555131757 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979585 | CATACTAATCCCTTA[C/T]AAATTGGTACAAGTA | 9169 |
rs555183224 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961271 | GTATCTGCTCTGGTT[A/G]TTCCACAAGGCTGAT | 9169 |
rs555224215 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941292 | TTATTGAGGTACAAT[A/T]GACAAAAATTGTATA | 9169 |
rs555244821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969813 | ACAATTACAGCTCAC[C/T]GCAGCCTTGAATTCC | 9169 |
rs555515203 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931960 | ACTACTCTAAAAAAA[A/T]AAAATCAACTTTGAG | 9169 |
rs555570255 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980369 | ATTATTTATGGATAT[A/G]TTTAGCAACCATAGC | 9169 |
rs555638870 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966694 | TCTTGGCAGAGAGAA[C/T]AGCCAATATGAAAGT | 9169 |
rs555761251 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973613 | TGATGCATTACTTAC[A/G]AGGGGGAGGGAGTTT | 9169 |
rs555785294 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968509 | ATTTATCATATAAGA[A/C]GGTATTAAAGCTTGG | 9169 |
rs555789185 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950718 | GTCCTGTTTGTACCT[G/T]GCATCAAGATTCATC | 9169 |
rs555800439 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970895 | GTGCAGTGTGGAAGC[A/G]AGTGCCAAAATAATC | 9169 |
rs555818810 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988757 | TTACCCCAGTGAAAT[C/G]TTAAAATGTACTCAA | 9169 |
rs555824490 | snp | G/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972871 | ATATATATCGATATA[G/T]ATATATATAGATATA | 9169 |
rs555873866 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942476 | ATGTACCAGATCACG[C/T]TACTCCTGAAAACAC | 9169 |
rs555890734 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924069 | TTGGCCAGGCTGATC[A/C]TGACCTCGTGATTCA | 9169 |
rs555896086 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923642 | TATTCCTTCAACTCT[A/G]TCTTACTGTCAGGAT | 9169 |
rs555913609 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957459 | CTATGTTGAACACTA[C/T]TGTTTGACTTCTTCA | 9169 |
rs555915797 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45926759 | TTTCTGTACCGATCA[C/T]TTCCTCGTGGACATC | 9169 |
rs555985892 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941588 | TCCCAAAAACCACCA[A/C]CATTCTACTTCCAAA | 9169 |
rs556032464 | in-del | -/CTAG | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954729 | CATGTATCACCGTGC[-/CTAG]CTTTTTTTTTTTTTT | 9169 |
rs556049131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949800 | GGTTGTAAATACAGG[C/T]CTGGCTCTCAGTAAA | 9169 |
rs556294099 | snp | G/T | 0.000399281 | 0.0141238 | missense | SCAF11 | GRCh38.p7 | 12:45926891 | GGGGACCTAGAATGA[G/T]ATCTGGACCTAGACC | 9169 |
rs556301343 | snp | A/G | 0.00547096 | 0.0520149 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974261 | TTTTGATGGTGGAGG[A/G]TCTTGCTTTGATGTT | 9169 |
rs556321411 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971482 | AAGACACCAGAATCT[A/G]ATGCATCATCAAACT | 9169 |
rs556357703 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973469 | GGTGAAAGGCATAAA[C/T]TGCTACATTTAAGAA | 9169 |
rs556359176 | snp | A/G | 0.00013182 | 0.00811742 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927571 | TTCATTGTTGTCCTC[A/G]CTAAAATGCTTCTGA | 9169 |
rs556363887 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45960072 | AAAAATATTCAACAA[A/G]AGTTAAAAATATAGA | 9169 |
rs556411381 | in-del | -/AT | 0.00953873 | 0.0683987 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989217 | CTGAGGTAGGTGGTG[-/AT]ATATGTAGAAATTAA | 9169 |
rs556440287 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920923 | CACAAATAATTTATC[A/G]TCTGCAACGGGTAGA | 9169 |
rs556480395 | snp | A/C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953085 | GGGAAAAAAGCTTTA[A/C/T]CACATCTGAATTAGG | 9169 |
rs556580725 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941451 | AAATTTCAAGTGTAC[A/G]ATACACCATTATTAA | 9169 |
rs556584522 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941087 | AAGAAATGACAACTG[A/G]AAGAAACCATCAATT | 9169 |
rs556623984 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979633 | ACAGAAAAAAGCAAT[C/T]ATCTTGCACAGTGTA | 9169 |
rs556625897 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988007 | AGATGAGTTTTGGGA[A/G]TAGCAAGAGAATGAT | 9169 |
rs556689248 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987621 | GTTGTTTTATACACA[A/G]TAGTTAGAGAAGACC | 9169 |
rs556743243 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938283 | TCACCTGAGGTCAGG[A/G]GTTCGAGACCAGCCT | 9169 |
rs556753478 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956366 | TAAAGATGACTTAGA[A/G]ATGCATACCATTAGT | 9169 |
rs556754519 | snp | C/T | 0.000399281 | 0.0141238 | missense | SCAF11 | GRCh38.p7 | 12:45928614 | TTTGCTTTTCTGACT[C/T]AGCTGAAGAGGGAAC | 9169 |
rs556771746 | snp | C/T | 0.000798403 | 0.0199641 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992087 | GCGGCGTCCCCTGCT[C/T]CCGCCCTGAGGACGT | 9169 |
rs556839621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924219 | TTCAAATTTTCTATG[C/T]CTCACAGAGGCACTT | 9169 |
rs556901635 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952927 | ACCACGTATCAAGAC[A/G]TGCTTATACAAGTAA | 9169 |
rs556906070 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955286 | CTCAGTTTCCCAAGT[A/T]GTTGGGACTACAGGC | 9169 |
rs556929046 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984635 | AGATTATCTCAGCTT[C/T]GGCTAGTGAAAGCCT | 9169 |
rs556963568 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976417 | TAATCTTTTCTGCAC[C/T]TAATTTATAAGTTAA | 9169 |
rs556990403 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45960016 | CATGCGGGAAAGGTG[C/T]TGGCTGCCATACCAT | 9169 |
rs556991584 | in-del | -/AAG | 0.00676609 | 0.0577691 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973398 | AAAAAAGAAAGTAGA[-/AAG]AAGAAGAAAAAGAAG | 9169 |
rs557067046 | snp | A/C/T | 0.00677088 | 0.0578511 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45919013 | AGAGCTTGGGTATTA[A/C/T]GTAACCATGATGCGA | 9169 |
rs557085310 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983905 | AGTTTAGTCTTATCC[C/T]TAATAGAGATGTGAG | 9169 |
rs557099316 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974371 | TTCAAGTATGCCACA[C/T]TGACACTCCTTTCAC | 9169 |
rs557101368 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982785 | AGTGTTGTTTTGGCC[A/G]CTGTCTTTCATGTTT | 9169 |
rs557179950 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966849 | TTGGGGAAATTCATA[C/T]CATACTATCTCCTTC | 9169 |
rs557225356 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933450 | TTGTATTTATATGAT[C/T]GTTAAAAATAACCCT | 9169 |
rs557244808 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944753 | GAAGACAGGAATATT[C/T]AACTGCTCATGTAGA | 9169 |
rs557308121 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951995 | AACTACTAGTATAGT[C/G]AAAGATGAGTTGGGC | 9169 |
rs557367902 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967592 | GAGGTTGCAGTGAAT[C/T]GAGATTGCGCCACTG | 9169 |
rs557404140 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958776 | AAGAGGATTCTGACA[C/T]ACCCAAAGACTTTTT | 9169 |
rs557535562 | snp | A/G | 6.59076e-05 | 0.00574016 | missense | SCAF11 | GRCh38.p7 | 12:45924904 | TGTTAAATGGATTGC[A/G]TTGGATGTTCATCAA | 9169 |
rs557559926 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921344 | AGACTTTGAACTGCC[A/G]AAGTTGTAATCTAGT | 9169 |
rs557625513 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989980 | TGGAGCCCCTTCCCC[C/G]CCCCCCGTAGGACCC | 9169 |
rs557658539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943148 | ACCATGTTAGACTTA[C/T]CAAATTTCCCTAGTA | 9169 |
rs557715413 | snp | C/T | 5.60041e-05 | 0.0052914 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922224 | GTGGGGGGTAAACTT[C/T]TTTCATGCTTAAAGG | 9169 |
rs557723308 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953212 | ATAGAAAACTTGACC[C/T]TAAGAAGGTTTGCTT | 9169 |
rs557744821 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983673 | GATTAGATCACCTAT[A/G]AAAGGTGACAATCAG | 9169 |
rs557778217 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956979 | ATAGTGGTGGATCTG[-/A]AAAAATTAGCTACAA | 9169 |
rs557805955 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982949 | GGATACAGAAGATGA[A/C]CAAGATAGCATATGC | 9169 |
rs557808004 | snp | G/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991042 | GTGTGCTCCTTATCT[G/T]TATGGTAATCTGATA | 9169 |
rs557847692 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964666 | GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAACGG | 9169 |
rs557869291 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990568 | GCGGCTTAAGCCACC[A/G]CTACTCCCCCTTCCC | 9169 |
rs557950332 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989043 | TCTTGCATCTTTTAA[C/T]CAAAATAGTGACATG | 9169 |
rs558013551 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988165 | GTTTATTTCACTGGG[C/G]AAGGTAAGTCAAGGT | 9169 |
rs558029300 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959360 | AGGCTATCCCTTGAC[C/G]TACTTAAAAATCGTA | 9169 |
rs558094929 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967527 | CAGGCACCTATAATG[C/T]CAGCTACAAGGGAGG | 9169 |
rs558230964 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981741 | TTAAGGTTGCAGGGA[A/G]CTATGGCCATCCCAT | 9169 |
rs558287283 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986398 | CTGCTGGTCTCAAAT[C/T]CCATCCACTGAGCCC | 9169 |
rs558302205 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970815 | TTACAGGTCTTTTAA[C/T]AAAATCAGTTTCCTA | 9169 |
rs558349730 | snp | A/G | 0.000114071 | 0.00755131 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931647 | ATTTTTGTTTAAATG[A/G]TTTAAAAAATTAAAC | 9169 |
rs558349787 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922874 | CATACAATAAAAAGC[G/T]GATATTTTTTCTCCT | 9169 |
rs558361498 | in-del | -/ATATATAG | 0.0256215 | 0.110247 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973006 | TAGATATATAGATAT[-/ATATATAG]ATATATAGATATATA | 9169 |
rs558412585 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993446 | AAGTTCAAATTAAGG[A/G]AGGAAATCATGCTGT | 9169 |
rs558418536 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923337 | AGTAACATTCTTAAA[C/T]GGGGCCTTATTTAGA | 9169 |
rs558444979 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950650 | TATAAACTAATTTGC[A/G]TTGATGGCAAAGTTA | 9169 |
rs558479062 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992345 | AGGGGAAAATGAGCT[A/G]GAGGCGTTAAAATGC | 9169 |
rs558493897 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975437 | ATCAATGATGTTAGC[C/T]AGGTCTTCTGGATAA | 9169 |
rs558559947 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963567 | ACCACCAATAGACCT[C/T]CACTAAAGAAACTTC | 9169 |
rs558576522 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953714 | AAAAACTAAGATGTA[C/T]AGAGGCCATGAATTT | 9169 |
rs558616898 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969983 | CTCACCGCAACCTCC[A/G]CTTCCCAAGTTCAAG | 9169 |
rs558640706 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981310 | AAGAGTCAAAAACGA[C/T]GAATGAACTCATCCC | 9169 |
rs558691625 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934576 | CTGTAAACCAGCATC[A/G]ATACCAGCACATTGG | 9169 |
rs558701149 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960293 | TTAGAGCAAAACATA[C/T]ACTCCGATTAAGTTG | 9169 |
rs558752935 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926046 | AGCTTATTATAAAAA[C/T]TACAAATAAGGATCA | 9169 |
rs558762036 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945700 | CACCACCTTGTCAGG[C/T]TAATTTTTTCTATTT | 9169 |
rs558820254 | snp | A/T | 0.000527053 | 0.0162249 | missense | SCAF11 | GRCh38.p7 | 12:45926773 | ATTTCCTCGTGGACA[A/T]CTCCAACCATCATTT | 9169 |
rs558835675 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938464 | ACTGTACTCCAGCCT[A/G]GGTGACAAGAGCGAG | 9169 |
rs558853181 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968905 | CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCC | 9169 |
rs559047820 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972773 | GACAATTAAAAGAAA[A/C]CACCACCAAGATGAT | 9169 |
rs559102995 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930255 | GCTTCTTGGGAGCAC[C/T]TCCTACATCACTAAT | 9169 |
rs559139018 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968660 | AATAATGGTAGTGAC[A/G]CAGGGCACAGTGGCT | 9169 |
rs559244599 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976093 | AACTGCAATAAAAAG[A/C]GGTATGCCTATATGT | 9169 |
rs559362820 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961482 | GTTATTAACTTTTTT[A/T]AAAAAAGTATGCATT | 9169 |
rs559435980 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943945 | AATCAGAATTAATCA[C/T]AGATGCTTATAAATG | 9169 |
rs559489303 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968758 | CTAGCCTGACCAACA[C/T]GGTGAAACCCCGTCG | 9169 |
rs559522560 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975139 | TGCTGTAAACGGATG[A/T]GCTGTCATCCAAGCT | 9169 |
rs559550258 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968009 | AGTAATTTGTGGTCA[A/G]TAGCCCTAAGAGGTA | 9169 |
rs559555706 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967058 | TATTTTCACATTTCC[C/T]CCTTTAAGCAAACTA | 9169 |
rs559584565 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983148 | GGACTTCAAGTCTAT[C/T]TCTCTCCCATTTATT | 9169 |
rs559615434 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966473 | AAAATAGTAAGTAAA[A/G]TATCTAGTATGTTAG | 9169 |
rs559617488 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974528 | TAACAATGTTCACAT[C/G]TTCAGCAAGAGCACA | 9169 |
rs559708798 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973948 | ATCTTGAATTCTTTA[A/T]AATAGGTTTGGCATT | 9169 |
rs559724328 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987016 | TAGCTCCTTCTATAT[A/T]AAGACAAATGATAGT | 9169 |
rs559731337 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958401 | AATATGGGTAAAATA[A/C]ATAACTTCCTAACTG | 9169 |
rs559762871 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944901 | TGCTACTGCTTACAG[G/T]AACTGGCCCACAAGG | 9169 |
rs559764700 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935851 | ATCTCTAAAGTATTC[A/G]ATACTGGTGAATTTG | 9169 |
rs559805094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951475 | GCAAATGAATAAAAG[G/T]TTCAGAATTTAAGTA | 9169 |
rs559829715 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944161 | CAGCAGTAAATTTTA[C/T]ATTGGTTCTTAGAAT | 9169 |
rs559868092 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920734 | ATGGCTAATGGCTAC[C/T]ACCTGGTCACCAAAT | 9169 |
rs559869281 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958887 | ACTAACTTTGATCTA[C/T]GTGGCCAAAATAAAT | 9169 |
rs559929148 | snp | G/T | 0.0130921 | 0.0798413 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957868 | TTTAATCACTTCTCG[G/T]CAACTGTGGGAAATA | 9169 |
rs560002943 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938812 | AAAGTTTAATAAAGA[C/T]ATAATTAGATGGATC | 9169 |
rs560015152 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971035 | AAGTGAAAGGCAAGC[C/T]AGAAATCGTCAGCCA | 9169 |
rs560140256 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949129 | AACTTTGGTGTGATA[C/T]GGGGAATCAACCAGT | 9169 |
rs560174864 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941079 | AGTGAGAAAAGAAAT[A/G]ACAACTGGAAGAAAC | 9169 |
rs560231407 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939597 | CAGCTACTTGGGAGG[C/G]TGAGACAGAAGAATT | 9169 |
rs560295703 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938876 | ATGCCTGAAAGGGAG[A/C]TCCTGTCTGTAAACT | 9169 |
rs560305361 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977644 | AACTAAAATATAAAT[G/T]GTTAACATTTTCAGG | 9169 |
rs560328608 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954979 | CTTAGGTTTGCCTAG[C/T]TTCATTTTAAGAAAA | 9169 |
rs560361468 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969776 | CAGTCTTGCTCTGTC[A/G]TCCAGGCTGGAGCGT | 9169 |
rs560577696 | snp | A/G | 0.000181625 | 0.00952782 | missense | SCAF11 | GRCh38.p7 | 12:45928007 | TCACTTAGGGGACAA[A/G]ATACAGGTTGGTACA | 9169 |
rs560610097 | in-del | -/T | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935814 | GTAATTCTCAGGTAA[-/T]TACTCAACAGCTTCA | 9169 |
rs560615078 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993631 | TACAAAAATTAGCCC[A/G]CATGGTGGCATGTGC | 9169 |
rs560631247 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953946 | TTGGTTAATTAACAA[A/G]AGACAACCACAATAT | 9169 |
rs560642955 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920229 | ACAAAGCTTATGAAC[C/T]AGCACAATCATTATG | 9169 |
rs560756111 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990154 | AGGGGCCCTCCCGGC[C/T]GCAGCCTCCCCCACT | 9169 |
rs560774832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970061 | CCACCACGCCCAGCT[A/T]ATTTTTGTATTTTTA | 9169 |
rs560841999 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970053 | GGTGCCCGCCACCAC[A/G]CCCAGCTAATTTTTG | 9169 |
rs560846582 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939816 | ACAGACAACAGTTTC[C/T]CAAGTAGTTCTTTTA | 9169 |
rs560846698 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948350 | TTAAATACATTTAAA[C/T]CCCACTTCATTTTTT | 9169 |
rs560887074 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963041 | TAGATCCAAGAAAAA[C/T]ACTTGTGAATTGGAA | 9169 |
rs560900737 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976900 | CAATGAGACCAAAAG[C/T]TCATTCTTTGAAAAG | 9169 |
rs560950994 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993816 | AAAAAAAAGAAAAAC[A/G]TGGTTCTAATACTGT | 9169 |
rs560981666 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955345 | GTAGAGATCGGGTTT[C/T]GCCATGTTGCCCAGG | 9169 |
rs561047896 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932906 | TAAATAAATCTAGCA[C/T]ATACACAGCTATACT | 9169 |
rs561121532 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931391 | ATAGACGTATTTACA[A/G]GTTACTATGCCTTAC | 9169 |
rs561166281 | snp | A/T | 3.31746e-05 | 0.00407262 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961783 | TTTCTAATAGACAAT[A/T]AAGACATATTGGGCA | 9169 |
rs561177626 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938725 | GTACGATACAAACAA[A/G]TATAATAAAGGCTCT | 9169 |
rs561196265 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939135 | TTATATAATTTTACT[A/G]AAGTCACAGGTGTTT | 9169 |
rs561202157 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992390 | ACAACAAAATTCTTA[C/T]GAAGGACCTTTCCCT | 9169 |
rs561251954 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952225 | CTCCCCTCAGCCACC[C/T]AGATGGCCACTCCAG | 9169 |
rs561307024 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973981 | AGCAAATATTTATAA[C/T]ACTTTCTGATAAGAT | 9169 |
rs561367996 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925530 | CTCCAGCCTGGGCAA[C/G]AACAGAGAAACTCCA | 9169 |
rs561424017 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960472 | CAACACAGATAAAAA[C/T]CTTTATTTGGGTGGC | 9169 |
rs561448923 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938002 | CAAACTCAACTTGCT[A/G]AGGTTTGATGGTATG | 9169 |
rs561463661 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942572 | AATTCAGTCATTCTA[A/G]CCACACTAACTTCCT | 9169 |
rs561470381 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991872 | TAAGCTCTGCTCCCC[A/G]CGCGCGGCTCACCCA | 9169 |
rs561526486 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941969 | CCCACTCAATGTGAA[A/G]ACAAGGACAAAGACC | 9169 |
rs561566336 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980969 | CCTAATATATCACAT[C/G]ATTTAGAATAGTTTG | 9169 |
rs561591353 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950142 | AGAAAACAAACCATG[A/G]AATGTGGAAGTCTGA | 9169 |
rs561596752 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953509 | TGATCACACCACTGT[A/G]CTGCAGCCTAGGCAA | 9169 |
rs561635499 | snp | C/T | 6.58968e-05 | 0.00573969 | missense | SCAF11 | GRCh38.p7 | 12:45926292 | ATCCAGATCTATCTG[C/T]TGGTGTATCAAATGA | 9169 |
rs561748783 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981298 | GAAACAGGGATGAAG[A/G]GTCAAAAACGATGAA | 9169 |
rs561844682 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930126 | TGATACCCTAAGTTT[A/G]TATCATTTGTTTACA | 9169 |
rs561900810 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956734 | TCTGACAATAGGCAA[C/T]ACTTTATCTAGTGTA | 9169 |
rs562019714 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957519 | TCATTTCTAGTTTAG[C/G]AGAGAAACCATGCCT | 9169 |
rs562048802 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930719 | ACCATGTGGTTTGAG[C/T]GTGTATATGTTTTGA | 9169 |
rs562080611 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965251 | GAAGGAGATTATAAG[C/T]AGAGATATTTGCATA | 9169 |
rs562162043 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988241 | CTAAAGGGAAGTTAC[A/G]ATGAAAATTATTCTA | 9169 |
rs562215979 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979786 | GTGCCCTCATATGAA[A/T]ATTTTACACATAATT | 9169 |
rs562230980 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986856 | CTATGTAAGAAGTGC[C/T]CTTCTCCTCCCACCA | 9169 |
rs562290296 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978743 | TGGTGTACCCTGGAA[A/G]GACTTCTGAGCAGAA | 9169 |
rs562318284 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949255 | GTCACTAGCCACATA[C/T]GGCCACTCAGTGCTT | 9169 |
rs562342272 | snp | A/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993451 | CAAATTAAGGGAGGA[A/T]ATCATGCTGTAAATA | 9169 |
rs562380655 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923544 | GTCAAATGGCTTGTA[G/T]TAAGTTGACAGGAGA | 9169 |
rs562382445 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956649 | AGAACACATTTCATC[A/G]AACTACTTAAAATCC | 9169 |
rs562383643 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940502 | GATATAGAGTCAGAA[A/G]ACTGGATCAAATTCT | 9169 |
rs562493971 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932947 | ATAAATTAAGGATTC[C/T]TTACTTTCTAAGGGG | 9169 |
rs562553552 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941872 | AAAGTTACACTGAGT[A/G]TGCTTGCCTCTCCTG | 9169 |
rs562703659 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964052 | ATACAAGTGGACAGT[G/T]TGGAAACAACTGTTT | 9169 |
rs562769287 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954138 | TGCATCAAATCTTTC[A/T]AAGACTCTCAAATCA | 9169 |
rs562771900 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971118 | TATTTAGAAAGTTCA[C/T]CAAGTGTTCTAAAAA | 9169 |
rs562777738 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920184 | GGTCAAAAACTGCTT[A/G]GAAATATTTTTATGA | 9169 |
rs562803764 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964564 | CCCAGCTGCTCGGGA[A/G]GTTGAGGCAGGAGAA | 9169 |
rs562940668 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935179 | TATTGACATTGTTCA[A/C]AATAAATCACACTAA | 9169 |
rs562991836 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931291 | TGTGTATATAGATAT[A/G]TGGAGAGACTATGTA | 9169 |
rs563020084 | snp | A/G | 0.000798403 | 0.0199641 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993721 | GAGGCGGAGGTTGCA[A/G]TGAGCCGAGATGGCG | 9169 |
rs563052323 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947746 | CACTGGTGTGATCAT[A/G]GCTCACTGCAGCCTC | 9169 |
rs563058853 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931197 | TGCCTTATTCACTTA[A/G]CCTAATGTCCTCCAG | 9169 |
rs563106621 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968671 | TGACGCAGGGCACAG[C/T]GGCTCACACCTGTAA | 9169 |
rs563119462 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932140 | TCCTTTGTATCCTTC[A/T]CCCTCCTTTCCAGGC | 9169 |
rs563126716 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963441 | AAAAATGAGTAATAT[C/T]TTCAAAGTGCTAAGA | 9169 |
rs563176073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950956 | TTTCATTCATGACTT[A/G]GTAGTGATACATCAA | 9169 |
rs563182876 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923761 | GATCTTGGCTCACTG[C/T]AATCTCCGACTACCA | 9169 |
rs563320817 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967919 | AGGATCCACAAGTAT[G/T]TTTGAATAAAAGCTT | 9169 |
rs563346189 | in-del | -/TG | 0.0154538 | 0.0865337 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965513 | GAGATGGGGTCTTGC[-/TG]TGTTTCCCAGGCTGG | 9169 |
rs563353003 | snp | C/G | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990655 | CCTTCCCTCGCTGTC[C/G]GCGCGCTAAGGTGAC | 9169 |
rs563361940 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975082 | AATCTTTTTATCTGA[A/G]CATTTGGTCTCAACA | 9169 |
rs563511274 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942866 | TATTTGCGTTTGTCT[A/G]CGAGAAGATCCCATT | 9169 |
rs563572196 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958794 | CCAAAGACTTTTTAC[G/T]TAATCACTTTAAAGT | 9169 |
rs563587622 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943660 | CCATACCCAGTTCCC[C/T]TCAAATCAGTCCAGG | 9169 |
rs563614729 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981870 | ATAATGTAAATAATC[A/G]TGCACACCAATTAAA | 9169 |
rs563644846 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993102 | TTTTTAAATTTACAA[C/T]ATAATAAAGAGGTAC | 9169 |
rs563651747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951393 | AACGTCCTTCAGATT[A/G]TCAGAGATCTAATAC | 9169 |
rs563684131 | in-del | -/AATC | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937708 | TTGGAAAATTATAAT[-/AATC]AAGACTGCCAGTGCT | 9169 |
rs563728334 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989428 | TAATCCAAAATGAAT[G/T]AACAACAGTCAGCTG | 9169 |
rs563755576 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965465 | AAGAAATTCATACAG[G/T]AACATTTTATTTTAA | 9169 |
rs563772461 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958278 | GTAGGAAATCATAAT[C/T]GTCACTACTACAATG | 9169 |
rs563779948 | snp | A/G | 5.23629e-05 | 0.00511651 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933112 | GTAAACACCTGAGTA[A/G]ATAATTTTTTATTTT | 9169 |
rs563885401 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975002 | AACATTTATCTCCGT[A/G]TATTTCCATCAGAGT | 9169 |
rs564009479 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45974112 | GTTTCCTAGTATATA[C/T]GTTTATATTATACTG | 9169 |
rs564022233 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933748 | CTCAACTAACTGTAC[A/G]TGATTTTAAAACCTC | 9169 |
rs564069133 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967199 | TTCAAGACCAGCCTG[A/G]GCAACACAGCAAGAC | 9169 |
rs564071036 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981505 | CCAAAAACCGAAACA[C/T]CATTCTCCCATTTTC | 9169 |
rs564110047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943619 | CATCTACTTGGAACA[C/T]ATCCCCCATGGACAA | 9169 |
rs564152146 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982294 | TCAGGTGAGTGATAG[C/T]TTATAAATTTTTTGA | 9169 |
rs564212583 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990141 | CAGCGAGAGGGAAAG[A/G]GGCCCTCCCGGCCGC | 9169 |
rs564260934 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979450 | TCTGAAATTCTACCC[C/T]GTTCTGTTTAAACAA | 9169 |
rs564280393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989488 | ATATATTGGAAGTAT[C/T]TCAAAATTCAACATT | 9169 |
rs564352754 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942704 | AACTTCTTACTTCTT[A/G]AAGGTCACTGCTCAA | 9169 |
rs564391167 | in-del | -/A | 2.04514e-05 | 0.0031977 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925098 | GAAAAAAAGCTTGTG[-/A]AAAAAAATCATGTTA | 9169 |
rs564416388 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950899 | TTCTCCTATTAACGG[A/C]ATCACTTATGTTTAT | 9169 |
rs564447214 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958219 | CAATAAATCCCATTT[A/G]CTTAACCTGTGTGTG | 9169 |
rs564451245 | snp | A/T | 0.0119091 | 0.0762411 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928871 | GTACCTAATAATATT[A/T]AAAAAAAAAAAAAAA | 9169 |
rs564465555 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969104 | TAAATAGCCCAATGT[C/G]CTACTGTACAGCTAT | 9169 |
rs564485264 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987778 | AGCCATTTGAGAAAA[A/G]AAGTTACATGACCTG | 9169 |
rs564509586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957677 | ATCACATTTTTAAAA[A/T]TAATACTTAAAAGAT | 9169 |
rs564509912 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966233 | AAGAACAGAAAGCTT[A/G]AGAACATTAGCAATT | 9169 |
rs564511983 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921069 | CTCACTGCAATCCCC[A/G]CCTCCCGGGTTCAAC | 9169 |
rs564517081 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958372 | ATCAATAAGTATATA[C/T]TGTTTTTGCCCACAA | 9169 |
rs564544553 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972158 | TGGCTACTGGGTAGC[A/G]CATATTGAAAAAGTA | 9169 |
rs564576177 | snp | G/T | 0.00358779 | 0.0422022 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921714 | AAACCAGTGCACTTA[G/T]AAGTTTCTAATTTAT | 9169 |
rs564770680 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924367 | AATCACTAGTTCCCA[C/T]CGTCCCCATATACCC | 9169 |
rs564844244 | in-del | -/AC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939808 | ATAAAGAGACAGACA[-/AC]AGTTTCTCAAGTAGT | 9169 |
rs564847102 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954724 | ACATGCATGTATCAC[C/T]GTGCCTAGCTTTTTT | 9169 |
rs564955591 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983203 | GTTTAAATTGGGGAT[A/T]TTGAGCTTAATGTAG | 9169 |
rs564997490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925087 | AATCTATCAAAAGAA[A/G]AAAAGCTTGTGAAAA | 9169 |
rs565009740 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975749 | ACTGTTGAGAAACAG[A/G]GAGGTCCAAGGAGAA | 9169 |
rs565018471 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990837 | TGTGAGCGGGAGGAA[A/G]GGCAGCTGCGCTGGA | 9169 |
rs565111897 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952115 | ATATTCTATGACTTA[A/G]TATTTTCCCCCCAAA | 9169 |
rs565115948 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935683 | TCTTTCATTTGGAAA[C/T]CTATCTCAGAAAGCC | 9169 |
rs565116029 | snp | C/T | 1.64917e-05 | 0.00287151 | missense | SCAF11 | GRCh38.p7 | 12:45926384 | CCTGAACTGTTTGAA[C/T]TCCCTGAGAGGGGTT | 9169 |
rs565118191 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968770 | ACACGGTGAAACCCC[A/G]TCGCTACTAAAAATA | 9169 |
rs565120786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937859 | TTAGAGTGTAAATCT[C/T]CAGTCTTTCATTGGG | 9169 |
rs565174721 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959582 | ATGAGAGGATGGAGC[C/T]TAATTTATAATGATG | 9169 |
rs565182292 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945863 | CTTATTCTTATTATT[A/T]TTTTTTTTACTAGAC | 9169 |
rs565571275 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45952416 | TTATAGGAGTAAGGT[G/T]GAGCACATTTTCCTA | 9169 |
rs565577891 | snp | A/G | 0.000798403 | 0.0199641 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45919063 | GTAACACTTCAATAC[A/G]TTTGTAAGGGATTAT | 9169 |
rs565618136 | in-del | -/T | 0.398354 | 0.201224 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954570 | AATCTAAGCTGTTAC[-/T]TTTTTTTTTTTTTTT | 9169 |
rs565633543 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959774 | GCAATTTATTAATAG[A/G]TTGCTCTCTTGTTAC | 9169 |
rs565718711 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921234 | GTGATCCGCCACCTC[A/G]GCCTCCCAAAGTGCT | 9169 |
rs565770686 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946145 | TCACTCCTCACTCAG[C/T]TACCATTCTCTACAA | 9169 |
rs565884170 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982536 | ACATGGTGAAACCGT[C/T]TCTACTAAAAATACA | 9169 |
rs565906517 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967420 | AGGCTGAGGCGGGAG[C/G]AGCGTCTGAGATCAG | 9169 |
rs565915598 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953081 | CAATGGGAAAAAAGC[-/T]TTACCACATCTGAAT | 9169 |
rs565918559 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970407 | GGATATAAATGGCCA[C/G]GAGGAAATATCACAC | 9169 |
rs565937807 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939873 | GCTATATCATGGTTT[A/C]TGTTCAGTGTAACTG | 9169 |
rs565986601 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965671 | ATAATTGCAATGAAA[C/T]GTCCAAATATGCATT | 9169 |
rs566002638 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937035 | TAGAACTTTATGAAG[-/T]TATTTGGTATGATTT | 9169 |
rs566074280 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981690 | GTACTAGGTACTCTG[G/T]AGGCTAAGGCAGGAG | 9169 |
rs566075442 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988860 | AAATATTATAGCTAA[A/G]ATGCAGCTACCCTAA | 9169 |
rs566110388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951051 | GACATGTTTTTTTGT[C/T]TTTTCAGGTAAGCAA | 9169 |
rs566137647 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989837 | GTAAAGTTTGGTTTC[A/C]CTAGCGGGCTTGGAC | 9169 |
rs566172979 | snp | A/G | 6.60208e-05 | 0.00574509 | missense | SCAF11 | GRCh38.p7 | 12:45927264 | ATGGAGACTGGGGCC[A/G]CTTCTTTTCTTGTGG | 9169 |
rs566246419 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942345 | GTGGCCTAGAAAAAC[A/G]TCACCTAAAATAAAA | 9169 |
rs566249339 | in-del | -/CA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964359 | CTTGCTATCAAAATG[-/CA]CAGTCTTATTGAACG | 9169 |
rs566260789 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923297 | TTCAGGTAATTATAT[A/C]TAAAGGGCCCTTTAA | 9169 |
rs566261985 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993909 | AGGACATTTTTATTT[A/T]AATGATCTCTGGCAT | 9169 |
rs566266757 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930655 | ACAGCTATGATTTAA[C/T]ACTGTATCTTTACAG | 9169 |
rs566353819 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977995 | ATTATGACTCCCAGT[G/T]AGGTTACACTCTTAT | 9169 |
rs566582526 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925819 | CAATTATCAAAAAAA[G/T]TAAAAGTGTACATAT | 9169 |
rs566585832 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947391 | GGTTTTAACAGCAAC[A/T]AAAAAAAAGAAACCT | 9169 |
rs566605303 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985316 | TGTGGCCAGTTTCCC[A/G]TTGCCTTTGCTGTTC | 9169 |
rs566734760 | snp | C/T | 8.23811e-05 | 0.00641746 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927403 | AGAAACAGTTTCAAC[C/T]TTTTCATCCGCAAGA | 9169 |
rs566768549 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938191 | CTTAAACTTTGTGGC[A/T]TAAAACTCTTCTTTC | 9169 |
rs566831890 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937113 | TGTGCTCTACTATTA[A/C]GGAAAAAATTTCCTT | 9169 |
rs566837066 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918715 | CCATCTCAAAAAAAG[A/G]AAAAAAAAGAGAATA | 9169 |
rs566872849 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941025 | CCTCAATCTTATTTC[G/T]GATCATCATTAGTCT | 9169 |
rs566897106 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976307 | TTCATTTCAAGAAGG[A/G]TGAGTAAAGTACAGT | 9169 |
rs566907026 | snp | C/T | 1.64792e-05 | 0.00287042 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922441 | AACAACGTGCACATA[C/T]TCCACTAAAGCCATA | 9169 |
rs566949662 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929230 | TGGAGCAATCATCGC[A/G]CACAGAAGCCTCAAC | 9169 |
rs566961552 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984434 | CTGTCAAATGGCATA[C/T]AATTTCTGTTTGTCT | 9169 |
rs567034906 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932738 | GGCACTTGATCAAAT[A/G]GTTATTTAGAAAAAC | 9169 |
rs567036318 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941827 | TGTTTGAACTCCATG[A/G]GTCTGCTTATTCATG | 9169 |
rs567100929 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970299 | GGTCTCCTAAAATGC[C/T]GGGATTACAAGCATG | 9169 |
rs567123000 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983435 | TGAACTACACATTCT[A/G]GCATGCCTTTCCACA | 9169 |
rs567140163 | snp | A/T | 0.00308066 | 0.0391259 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991958 | TCTGTTCGCGCGTGC[A/T]GCGCTCTCCAGCCAC | 9169 |
rs567162503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985258 | TCACCAGGAGAACTC[C/T]GACTCATTATCATTA | 9169 |
rs567187122 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980159 | CATTAAGTAGTAGGA[C/G]TGGAACCCATTAGCA | 9169 |
rs567214002 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964940 | GAAAGTGTGTGTGTG[C/T]GTGTGTCTACTAAGG | 9169 |
rs567275387 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968803 | AAAAATTAGCCGGGC[A/G]TGGTGTAATCCCAGC | 9169 |
rs567280465 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967543 | CAGCTACAAGGGAGG[G/T]TGAGGCAGGAGAATT | 9169 |
rs567300663 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923256 | CACAAAGCAAACCAA[A/C]CTTAGTACTAAAGAA | 9169 |
rs567312567 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939315 | TATTCATTAGTTTGA[G/T]TACTGTATAACAAAT | 9169 |
rs567337169 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976259 | TTAGAGCTACCACTA[A/T]AAACATTAGTCAACG | 9169 |
rs567375420 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947240 | GCTTAAGTTTCAAAT[A/G]TATTAGAACAAGTTA | 9169 |
rs567440094 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961019 | TTTACTTCAAAGTAT[G/T]TGGCCCAAATTGAGT | 9169 |
rs567469527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983296 | AAAGAAGACTAGATA[C/T]CAAAAAAGAAGGCCT | 9169 |
rs567496876 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953560 | GAAACATAGATAAAT[A/T]AAATTAAAAGTGTAA | 9169 |
rs567562483 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945130 | GGATTTAACACAATG[C/T]ACAGAGTTCTGAGGA | 9169 |
rs567623545 | snp | A/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944332 | TGCTTCAATTTCACT[A/T]TAATAGTAAAATTTC | 9169 |
rs567674762 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924088 | CCTCGTGATTCACCC[A/G]CCTGGGCCTCACAAG | 9169 |
rs567736898 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936873 | GATGGATAGTTTGAT[A/T]GGTTATAGAATTGTC | 9169 |
rs567741240 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973271 | ACCTAAAAAACAAAG[A/G]GAAAAACATTGAAAA | 9169 |
rs567801355 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972486 | GCTAATCAGGTGACT[A/G]GGGCAGGAGGATCCC | 9169 |
rs567830127 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924640 | AATTGTTTTTGAATG[C/G]CAGGATGCCTTTTTT | 9169 |
rs567842427 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933906 | GCTACTTCTCAATCA[C/T]ATAAACAGCTTATAT | 9169 |
rs567889768 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936127 | AACACCCTTATACTA[C/T]TCTATGTGTGGTTTT | 9169 |
rs568001841 | in-del | -/CA | 0.0164234 | 0.0891177 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944298 | TTAACCACAGAAGTC[-/CA]GAGATCAAAACAACT | 9169 |
rs568020109 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968772 | ACGGTGAAACCCCGT[C/T]GCTACTAAAAATACA | 9169 |
rs568146047 | snp | A/G | 6.5925e-05 | 0.00574092 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928165 | TTCAAGAATATTTTC[A/G]GAAATCTCACTTTCC | 9169 |
rs568150969 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987158 | TTAGCCCAGGAATTT[C/G]AGACCAGCCTGGGCA | 9169 |
rs568537545 | snp | A/C/G | 2.26375e-05 | 0.00336426 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964154 | TTTAGGGTACATACA[A/C/G]TTTTCTTCTTCATTT | 9169 |
rs568587578 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979313 | AACATTGAAACCACA[C/G]AAAAATCCTAAGAGT | 9169 |
rs568651153 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987275 | AACAAAAAACAAGGA[C/T]CCCTGAAATGAACAT | 9169 |
rs568693265 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970595 | ATTAGTTTCTAGTTC[A/G]GTTTCTAAGAAGATT | 9169 |
rs568715420 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964405 | GTGCACGGTGGCTCA[A/C/G]GCCTGTAATCCCAGC | 9169 |
rs568732409 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923987 | TCCTTAGTAGCTGGG[A/T]TTACAGGCGCTTGCC | 9169 |
rs568785291 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986213 | TGAATTTCAGAACCA[C/T]GTATCTAATTGCTTA | 9169 |
rs568785450 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972240 | CCTACAGAAAGCTAA[C/T]TGGAACTTGTGACCA | 9169 |
rs568794897 | snp | C/T | 0.00159617 | 0.0282053 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921099 | CTGATTCTCCTGCCT[C/T]AGCCTCTCGCATAGC | 9169 |
rs568801801 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991473 | AAGATGAGGTGGGAG[A/G]ATCGCTTGAACCCGG | 9169 |
rs568817646 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977205 | AACAAATTTATATTC[C/T]GCTCCTCATCAAAAC | 9169 |
rs568853170 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958973 | TGTTTTTAAGAATGT[A/G]TTCAATGCCTAAAAT | 9169 |
rs568957675 | snp | A/C/G | 6.61425e-05 | 0.00575045 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926593 | CTTTTCTGGATTTCT[A/C/G]GTTCTTGGATCAGGC | 9169 |
rs569142793 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934987 | TTACCATTTAGCCAC[C/T]GGCACCCACTTCAGG | 9169 |
rs569156140 | snp | C/T | 4.06182e-05 | 0.00450638 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934136 | ATAATTATTAAACAT[C/T]AAGTATAAACAGCAT | 9169 |
rs569240539 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962193 | ACTGTTAAATTTCTT[C/T]TGTGTTCTTCCTAGG | 9169 |
rs569261380 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45963298 | CCATGCCTAGAAACA[A/G]TGGAGTAAAACTGTA | 9169 |
rs569261990 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973894 | ATGGAAGATCAACAG[A/G]AACAGTAAATGCCTG | 9169 |
rs569297307 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45929620 | GGAGACTTCTAATCA[C/G]TTCCTCAAAGCCTCC | 9169 |
rs569308141 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969790 | CGTCCAGGCTGGAGC[A/G]TGGTGGCACAATTAC | 9169 |
rs569359889 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921349 | TTGAACTGCCAAAGT[C/T]GTAATCTAGTAAGTC | 9169 |
rs569453110 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969080 | ATTTTTGTGAAGTTT[C/T]AGTTAATTTAAATAG | 9169 |
rs569462320 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939666 | TCGTGCCATTGAGAT[C/T]GTGCCATTGCACTCT | 9169 |
rs569490124 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977096 | AACACCAAATCAACA[A/C]AATCTCTTCCAGAAA | 9169 |
rs569501560 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924299 | AATGGATAATAAACA[C/G]CTTTATCCAGTGTTT | 9169 |
rs569509196 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976351 | AGAGCCCACATTCAC[A/G]TAACTTTTATTACAG | 9169 |
rs569545778 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939172 | TAAAAACTGTACAAA[A/C]CTCAAGGGGCTTGAC | 9169 |
rs569550945 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985173 | AACCATGAATTGGTA[C/G]CAATTTCTCCAATTT | 9169 |
rs569580743 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959176 | TCAGGAGCTGTGGCA[C/T]AAGAATCGCTTGGCC | 9169 |
rs569610152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984532 | GTTACTTTTGTCCCA[C/T]TGGTAATTAACATGC | 9169 |
rs569724833 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958472 | TCATCAGTTCAAATG[C/T]CTTTGATTAATTTTA | 9169 |
rs569783896 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966666 | TATCATCCAGTGCTT[A/C]CAGGCTAAGCATTCT | 9169 |
rs569890539 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989765 | AAGGAGTGAAAAAGG[C/G]TGATGCTTAGAAGCG | 9169 |
rs569942013 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973516 | ACAGAATAATCCCAA[A/T]GAAATCCATGCCTGG | 9169 |
rs569976172 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951814 | TTTTCCATAAAATTA[-/T]TTTTATCTCTATCTT | 9169 |
rs570004773 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981017 | AGGTGATTTATAAAT[G/T]AACAAAATAAAGAAA | 9169 |
rs570033863 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988725 | GAGTATACTTACAGT[A/G]AGCAAACATTCAAAT | 9169 |
rs570072708 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942279 | CATACAGAATGGAAC[C/T]ACTTATCATCATCTC | 9169 |
rs570134140 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966607 | GTGATAAAGGGACAT[G/T]TGAACTGGCAATCAG | 9169 |
rs570165974 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45950333 | TAAAGGTCTAGGGAA[G/T]GCACTTAAGAGAATG | 9169 |
rs570202550 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965786 | AATAATTTACACATG[G/T]TAGTTTCTACATTAA | 9169 |
rs570217756 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932598 | CTCAGGCAGCGACCC[C/T]AATCTTTACTTAGGA | 9169 |
rs570227355 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957861 | CCAAATTTTTAATCA[C/T]TTCTCGGCAACTGTG | 9169 |
rs570227495 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949642 | GGAGAGAAAACTGGA[A/G]AAGTCCCAGATATTT | 9169 |
rs570321560 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949391 | AATTTTAAAATATTA[C/T]ATGTTGAGCTAATAC | 9169 |
rs570323388 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964983 | GTGTGTATGTGTGTG[C/T]CTCTACTGAGGAGGG | 9169 |
rs570335025 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983361 | ATAGACACATAGATA[C/T]CAACAAACCTGGAGT | 9169 |
rs570374788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924428 | AAAGCACCCACCACT[C/T]GATTCTAATTTGGCT | 9169 |
rs570460257 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930467 | TTTTGTTTTTTTTTT[G/T]TTTTGAGACAGGCTG | 9169 |
rs570570976 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972680 | AGTTTTGTAACATAA[C/T]ATTCAAAATGTACAG | 9169 |
rs570587131 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935389 | AATGTTAGTGGAAGA[C/T]GAACAGGCTGAGTTC | 9169 |
rs570634307 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980236 | ATGAGTATTCAAACA[A/T]CAAGAAGTGGTAACA | 9169 |
rs570642821 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980954 | TGTCTTAGGACATAA[C/T]CTAATATATCACATC | 9169 |
rs570649939 | snp | A/G | 3.29478e-05 | 0.00405867 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926821 | CCGGGGAGAGTAACT[A/G]TCTCTGTCAATTCTA | 9169 |
rs570735210 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920543 | ATGCCAGTTAAAATA[A/G]TGGCACAATAAACAT | 9169 |
rs570739084 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988512 | GGTGCCAAAGGACGA[C/T]AGAGAGCTAAGTAAC | 9169 |
rs570804087 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987970 | TAAGTTCATAGACAC[A/G]ACTTAAAAAAATACA | 9169 |
rs570858642 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949540 | ACAGCACTAGTTAGA[G/T]GAAAGAATAGGGGTC | 9169 |
rs570864049 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973705 | AACATCCTTCAAATG[C/T]TAAAATGGAAAAGAA | 9169 |
rs570975722 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956678 | CCTTTCATGTTCTCC[A/G]AGATACCAGTTGGGG | 9169 |
rs570993519 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992552 | CCAACAGAATAAGGG[C/T]GTAGCTTTTTTATGT | 9169 |
rs571078945 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964301 | AAAAGAACACAGTAC[A/G]AGCCAAGCCAGTTTG | 9169 |
rs571088825 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986647 | TTTGGCTGTGTCCCC[A/G]CCCAAATCTCTCTTG | 9169 |
rs571107919 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971447 | AGACTCAGGAGTAAA[C/T]AATAGCATATGGACT | 9169 |
rs571132233 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938253 | CCAGCACTCTGGGAG[A/G]CCGAGGTTGGCGGAT | 9169 |
rs571145140 | in-del | -/TGTTA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952043 | TGATGTAAAGCTGGC[-/TGTTA]CACTAAACTTGGGCC | 9169 |
rs571296651 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933358 | CACTTACAAGCATGT[A/G]AGCTCTTTTCTATTT | 9169 |
rs571319100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945413 | AAATGAAATCTATCA[C/T]GCACTGATTTTGGTA | 9169 |
rs571329596 | snp | A/C | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991052 | TATCTTTATGGTAAT[A/C]TGATATTGAAAAGAG | 9169 |
rs571339550 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974307 | ATCACAGGATGGTAG[C/T]TGCTGAAGGGCAGGG | 9169 |
rs571359876 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934013 | AGGTTTTCTCTTTGC[C/T]AGAGCTAGTTTACCT | 9169 |
rs571366939 | snp | C/T | 0 | 0 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953348 | TTTCTTAAGAGATTA[C/T]ATTAATGCTACATTT | 9169 |
rs571381134 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988349 | TAAAAGTTCAGTATT[A/G]AGTTGATGGGTAGTA | 9169 |
rs571386287 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982774 | ATTTTTATAACAGTG[G/T]TGTTTTGGCCGCTGT | 9169 |
rs571422615 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925731 | TTATCTTGCAATGTT[C/T]TTAACAAGAAAAAAA | 9169 |
rs571432376 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960814 | CCCAATTATGTAATA[C/T]GCAATTAATTCCAAC | 9169 |
rs571448657 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981829 | GGAAGAAAATAGAGG[A/G]ACAAACATTATTATA | 9169 |
rs571448717 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990319 | CCAGACAGCTGCCCA[A/G]GCCCATCCACCCCGC | 9169 |
rs571456214 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968010 | GTAATTTGTGGTCAA[C/T]AGCCCTAAGAGGTAA | 9169 |
rs571509230 | in-del | -/T | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970201 | CCCGGCCTCAACTAA[-/T]TTTTTTTATTTGTAG | 9169 |
rs571571908 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967547 | TACAAGGGAGGGTGA[A/G]GCAGGAGAATTGCTT | 9169 |
rs571633982 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974813 | TACGAATGTTCTTTA[C/T]GGCATCTAGAATGGT | 9169 |
rs571679490 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45936248 | CCAGGTTCAAGCAAT[G/T]CTCCTGTCTCGGCCT | 9169 |
rs571805106 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943437 | TTTTGAGAGAGCCCA[C/T]GCTCACCTAACTTTT | 9169 |
rs571847771 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943118 | TAATCTATTTCAATA[C/T]AGGAAGAAAAACTGA | 9169 |
rs571955519 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977496 | AATCTTGACTGTAGT[A/G]GTAATACAGATCTAT | 9169 |
rs572012040 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982120 | TTATATCTAGTTCTG[C/T]GGCAGTTTTGAAACA | 9169 |
rs572048244 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952632 | TTAAAATTCCTGTGC[A/G]TCAACTCTAAGAGTT | 9169 |
rs572065273 | snp | G/T | 0.0023933 | 0.0345097 | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990531 | GGCGAAGCAGGGAGC[G/T]ACCCAGGTTGCGCTG | 9169 |
rs572139165 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45990010 | CTGCACCCGGACGGG[G/T]ACAGGCTTCGCCAGC | 9169 |
rs572239333 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933728 | ATCGTATTCTGTGCT[A/G]CTGGCTCAACTAACT | 9169 |
rs572404439 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942255 | TTGTGTTTTCAAGGA[G/T]CAATGGTACATACAG | 9169 |
rs572408111 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938659 | AGCATATCCCTAAAC[A/G]TGTTTCATGAAACAC | 9169 |
rs572417804 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981115 | GATTGAGTGATATTC[A/C/G]GATTATCACCTAAAT | 9169 |
rs572536642 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980481 | GATTAACTTCATTTT[A/G]CAGTGATACTGTCAT | 9169 |
rs572594017 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988091 | TCAGAAGCAAGACAA[G/T]GTGCAAGGTTATTAA | 9169 |
rs572608316 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987692 | AGATGAAGTCAGAGA[C/G]GAAGAAGAGACTTAA | 9169 |
rs572645705 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949812 | AGGTCTGGCTCTCAG[C/T]AAAGAAGTCTAGGAC | 9169 |
rs572769079 | snp | A/C | 0.00159617 | 0.0282053 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992267 | TCTTTGGAGTTTTTC[A/C]GTGTACTGTTTTTGA | 9169 |
rs572799969 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957070 | AGCCCTGATCATCTA[C/T]TGCATAGGCGTAATA | 9169 |
rs572813889 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953261 | TATATTTTTTAATAA[C/T]GCATTGTCTAGTTCG | 9169 |
rs572817223 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932937 | TGTTAAACAGATAAA[A/T]TAAGGATTCTTTACT | 9169 |
rs572829799 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962644 | CAGCTGAAATGTGAA[C/T]AGTAATATCAAGCAA | 9169 |
rs572832261 | snp | A/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991253 | GGGCTTTCCCATGTC[A/T]TAACCCCACATCACA | 9169 |
rs572893036 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45976550 | AAGGGGTAACTACTA[C/T]ACCCAGTTCCCTTCA | 9169 |
rs572893073 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969929 | TTAAGACGGAGTCTC[A/G]CTCTGTCGCCCAGGC | 9169 |
rs572953985 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45969378 | CTTTCTGCTGTTACA[A/C]AACAGAGCTCCTTTC | 9169 |
rs572958653 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984829 | CCTCCCATGTAGCTG[C/G]GATTACAGGCATGGG | 9169 |
rs572987249 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, missense | SCAF11 | GRCh38.p7 | 12:45960182 | AGAAACCTGGAACAT[A/G]TACATCAGGGTAAAG | 9169 |
rs573004598 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933705 | AAGTTCTAAAATTAA[A/G]TCACACAATCGTATT | 9169 |
rs573049989 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959500 | AAGGCTGAAGACACT[C/T]ATTCCTGATCCTGAA | 9169 |
rs573089598 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946517 | AATCTCAGAAAAAGC[A/G]GTTAAATATGGGGAC | 9169 |
rs573089602 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919519 | GATAAATAATAAGAG[A/G]AAATGTAACTCCACA | 9169 |
rs573109108 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45938371 | GCGGGCACCTGTAAT[C/G]CCAGCTACTCAGGAG | 9169 |
rs573109678 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967677 | TTTAAAAACTGTTTA[A/C]GCATTCCAAAGTTTT | 9169 |
rs573116757 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945673 | TCCTGAGTAGCTTGG[A/T]CTACAGGCATGCACC | 9169 |
rs573161750 | in-del | -/A | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45942278 | CATACAGAATGGAAC[-/A]CACTTATCATCATCT | 9169 |
rs573165838 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45935528 | ATAACACTCTTAGAA[A/G]TAACCATGTTCCTTC | 9169 |
rs573247097 | snp | A/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961416 | AGTACACTGAAAAAT[A/T]AATTACTGCATTTCT | 9169 |
rs573256315 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930481 | TTTTTTGAGACAGGC[C/T]GTTGTTCTGTTGCAC | 9169 |
rs573428819 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974981 | TGTTGTGTTAGCAGG[C/T]ATGGCAACATTTATC | 9169 |
rs573489815 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982882 | TTGGAATATAAAGAC[C/G]GATTAAGATACTGTA | 9169 |
rs573514279 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974566 | TCAAGAAACCACATT[C/T]TTTGTTCATCCCTAA | 9169 |
rs573653513 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984783 | CACTGCAAACTCCAC[C/G]TCCCAGGTTCAAGCG | 9169 |
rs573689553 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983950 | AAATTTACTCAAGAG[G/T]GTTTAAAGATTGAGA | 9169 |
rs573691102 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968682 | ACAGTGGCTCACACC[C/T]GTAATCCCAGCACTT | 9169 |
rs573722307 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45937450 | TGCTTTTGTCTTTGT[C/T]TTGATCTCTATTATG | 9169 |
rs573837858 | snp | C/G | 0.00279162 | 0.0372561 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990681 | GTGACGACGGCGGCA[C/G]CCGGACTCGCCACAT | 9169 |
rs573906545 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974411 | CTCTGTGTACAAGAT[A/G]CTATTTGACAGCATT | 9169 |
rs573911339 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945527 | TCTATTGAGTTGTAT[C/T]ATCTCAGTCTTTTTT | 9169 |
rs573935762 | snp | A/G | 0.000198275 | 0.00995481 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992090 | GCGTCCCCTGCTCCC[A/G]CCCTGAGGACGTCGC | 9169 |
rs573946121 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968511 | TTATCATATAAGAAG[G/T]TATTAAAGCTTGGAA | 9169 |
rs573969604 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45982015 | CAAACAATAATAAAC[A/G]ATGGTTGGAATGGCT | 9169 |
rs573972002 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932003 | ATAAAATGCAGACTT[G/T]AAGCGTACATTTGCT | 9169 |
rs573972553 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45959458 | AGAATGTGTATGACA[A/G]CCTAGGCATAAGGCA | 9169 |
rs573977377 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944781 | AGATAAATATGTTAG[A/C]GGTGCTTTTATTTCT | 9169 |
rs574033873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923649 | TCAACTCTATCTTAC[C/T]GTCAGGATTCTATTT | 9169 |
rs574035387 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45967605 | ATCGAGATTGCGCCA[C/T]TGCACTCCAGCCTGG | 9169 |
rs574048914 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930725 | TGGTTTGAGTGTGTA[C/T]ATGTTTTGATAAATT | 9169 |
rs574125052 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966924 | TAACTCAATGTGATA[A/G]AATGTCATTTGAAAG | 9169 |
rs574177015 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964439 | TTGGGAGGCCGAGGC[A/G]GGCGGATCACAAGTT | 9169 |
rs574231562 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966559 | AAAAAGAGGAAGCTG[C/T]TGTTTCATACAGAAT | 9169 |
rs574242874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971749 | GTTCCTCATGTCCCA[A/G]TTCCCAAATGATCTG | 9169 |
rs574287543 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989981 | GGAGCCCCTTCCCCC[C/G]CCCCCGTAGGACCCT | 9169 |
rs574299516 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970949 | ACTATGCTCTACAAT[C/G]ATCAAAAACCTAATT | 9169 |
rs574316404 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984224 | GTCTTGACTTTCATG[A/T]CCTTGTTTGTACTCC | 9169 |
rs574361659 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978272 | GGACAGAACACAAAG[A/T]GTTGGTTACACAATC | 9169 |
rs574368929 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | SCAF11 | GRCh38.p7 | 12:45926253 | GCAAAGTCTTTCTCA[C/T]GGCCCAGCTGGATGC | 9169 |
rs574394905 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956372 | TGACTTAGAAATGCA[C/T]ACCATTAGTGGCTAA | 9169 |
rs574422955 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977504 | CTGTAGTGGTAATAC[A/G]GATCTATACATGTAT | 9169 |
rs574448617 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945966 | AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA | 9169 |
rs574457859 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975224 | TGGAATTTTCAGAAC[A/G]GTCAGTGAGCACTGG | 9169 |
rs574586579 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947581 | CATAAGTAACTTGAT[C/G]AGTGCTATTTACAGT | 9169 |
rs574604261 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918970 | TGCCATTAAAATATA[C/T]GCTTATAGCTAACTC | 9169 |
rs574647554 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955236 | ATCACGGCTCACTGC[A/C]ACCTCAACCTCCTAG | 9169 |
rs574651799 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981534 | TCTGAGGAATAAATA[C/T]AATCCGTCATCCTTG | 9169 |
rs574668873 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919747 | ACATGGAACACACAC[G/T]TGTTACTGTCACGGA | 9169 |
rs574709124 | snp | G/T | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986613 | TTTAACAATAAGATA[G/T]TTATACTGCTTGATA | 9169 |
rs574709193 | in-del | -/ATAT | 0.0119091 | 0.0762411 | intron-variant | SCAF11 | GRCh38.p7 | 12:45973021 | TATATAGATATATAG[-/ATAT]ATATATAGATATAGA | 9169 |
rs574738421 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45985861 | AGCTTCACATTGTTA[A/C]ACTCAACAGAATTTT | 9169 |
rs574813212 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992678 | ATATATATTTAAAAT[C/T]TAAATATATTTTTAA | 9169 |
rs574914030 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988042 | GATATTTTAACTCTG[A/G]GCTCTACTCAGCACT | 9169 |
rs574997311 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962454 | TAGAGTAATGTGTGT[A/G]TACATTTGTATTATG | 9169 |
rs575097332 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952984 | TGATCATTTAACACA[C/T]TTTCACAAAGCTCAC | 9169 |
rs575098386 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45977455 | AACACAGTTTTTGGC[A/G]GGGGTGGGATGATAG | 9169 |
rs575110769 | snp | A/G | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918810 | TGAAAATGAAAGGTT[A/G]CAACATATTATGTGC | 9169 |
rs575155254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924280 | AAAATGAAACACAGA[C/T]GGTAATGGATAATAA | 9169 |
rs575187512 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45984934 | TCCTGACCTCAAGTG[A/T]TCCACCTGCCTTGGC | 9169 |
rs575229881 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45962924 | CCAAACCTAAGAAAA[G/T]AAGCTGTCTTGAGTG | 9169 |
rs575266514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45955303 | TTGGGACTACAGGCA[C/T]GCACCACCATGCCCA | 9169 |
rs575275113 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970888 | AATTCTCGTGCAGTG[C/T]GGAAGCGAGTGCCAA | 9169 |
rs575284059 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45970023 | GCCTCAGCCTCCTGA[A/G]TAGCTGGGATTACAG | 9169 |
rs575324455 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953768 | TAATAAACTCGAGCA[A/G]GTTACAGTCTCTCTG | 9169 |
rs575327722 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954738 | CCGTGCCTAGCTTTT[C/T]TTTTTTTTTTTTTTT | 9169 |
rs575353805 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930596 | AACAGGTGGCGGCCA[C/T]AAAAATTGTTACACT | 9169 |
rs575384386 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961186 | TCTGCCTCTTAAACT[A/G]TGAGATCTTGACCAA | 9169 |
rs575388653 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953123 | ACCTTACTATATTAA[A/G]TTGGTTCAGACTGGA | 9169 |
rs575391786 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932875 | ATAAATCTTAATATT[C/T]GGGTTCTCTCCCTTT | 9169 |
rs575402200 | snp | G/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921896 | GTGCAGACCTATATT[G/T]ATTTAGAACAAAACA | 9169 |
rs575409322 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933491 | TCTTAAGTGACAGAA[C/T]TTTTTAAATAAAGTC | 9169 |
rs575475313 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951041 | ACTCAACTCAGACAT[-/G]TTTTTTTGTTTTTTC | 9169 |
rs575496840 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939505 | GTTTGAGACCAGCCT[A/G]ACCAACATGGTGAAA | 9169 |
rs575537300 | snp | C/G | 0.00119737 | 0.0244387 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992346 | GGGGAAAATGAGCTA[C/G]AGGCGTTAAAATGCT | 9169 |
rs575560498 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45947404 | ACTAAAAAAAAGAAA[A/C]CTGTATATTTAAAAA | 9169 |
rs575576277 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946711 | CAAGAATTAAAAGTA[C/T]TTCTACCAAAAGGTT | 9169 |
rs575599071 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943174 | TAGTAAAAAGTAACA[G/T]CACAGCAAAACTATT | 9169 |
rs575619411 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920843 | TTTACGCCAGTGCCA[C/T]GAGTCTTGTAATTCT | 9169 |
rs575680018 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993296 | TACCAGGCACTTAAA[A/G]TATCAGTCCTGTCAC | 9169 |
rs575824328 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45968664 | ATGGTAGTGACGCAG[A/G]GCACAGTGGCTCACA | 9169 |
rs576068200 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975530 | GCTTCTTTCCTTAAA[A/C]TTCATGAACCAACCT | 9169 |
rs576079679 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979589 | CTAATCCCTTACAAA[C/T]TGGTACAAGTAGTTA | 9169 |
rs576173562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966023 | ACAATAAAAGTTGGA[C/T]GAGGAATATTTCCCA | 9169 |
rs576265269 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45965192 | TAAGTGAATTTTTTT[A/T]AAAAAGATAGATACG | 9169 |
rs576506728 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980312 | GCCTTCTTTATCACT[A/G]TATTACTAGGATCCA | 9169 |
rs576519089 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45957285 | AGCTTTACTGAATTA[C/T]ATTACTTAAAAGTAG | 9169 |
rs576527709 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980134 | AACATGCCCAAGATC[A/G]AAAAGCCAGCATTAA | 9169 |
rs576546266 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45940952 | TGGGACTACAGGTGT[A/G]TATCACCACACTTGG | 9169 |
rs576565857 | snp | A/T | 0.00119737 | 0.0244387 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921825 | CTTTAAACCCTTTAC[A/T]TTCCCTTGAATTTTG | 9169 |
rs576578367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979745 | AGATAAGTACAATTA[C/T]GTTACATAAATGTAT | 9169 |
rs576696879 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923498 | ATTAAAGTGCCCTCA[C/T]TTTAAAGCCTGGAAA | 9169 |
rs576735841 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45941829 | TTTGAACTCCATGGG[C/T]CTGCTTATTCATGAA | 9169 |
rs576739566 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948987 | AGAGTAGCTAGATGT[A/G]AAATTGGTGAAATGT | 9169 |
rs576797550 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45949917 | AGAAAGAAAGTATAC[C/T]GAAAGAATTTAAATG | 9169 |
rs576802265 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956287 | TGTTTGTGGGAATCT[C/T]GAACATCTATCTCTC | 9169 |
rs576907604 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933738 | GTGCTGCTGGCTCAA[C/T]TAACTGTACGTGATT | 9169 |
rs576986416 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45939599 | GCTACTTGGGAGGCT[A/G]AGACAGAAGAATTGT | 9169 |
rs577016210 | snp | C/T | 0.000399281 | 0.0141238 | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918801 | TACGTCAAGTGAAAA[C/T]GAAAGGTTACAACAT | 9169 |
rs577019596 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981323 | GATGAATGAACTCAT[C/T]CCTAAAACAAACTAT | 9169 |
rs577038569 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926074 | TCATTTCAACTCATA[C/G]AAATAACATATTAAA | 9169 |
rs577104562 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45971097 | GTTTTTCAAAGCTAA[C/T]ACATTTATTTAGAAA | 9169 |
rs577111144 | snp | C/G | 0.0023933 | 0.0345097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45979617 | TTATTATAAAACCAA[C/G]ACAGAAAAAAGCAAT | 9169 |
rs577173999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45978508 | TGACAAAAAGCAAAA[A/G]AGCAGTGAGATGTTA | 9169 |
rs577212909 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | SCAF11 | GRCh38.p7 | 12:45946200 | CAAGAAACAAAATAC[C/T]ACTGCAATGCCTTCT | 9169 |
rs577314403 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45987503 | TCACAGTGAAGAAAA[C/T]AAACAATAAACCTAA | 9169 |
rs577377818 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | SCAF11 | GRCh38.p7 | 12:45986619 | AATAAGATAGTTATA[C/T]TGCTTGATATGGTTT | 9169 |
rs577396768 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950102 | AAGCCGAAGGAATTA[C/G]AGGGTAGTCAGCAGC | 9169 |
rs577453093 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45954717 | CTGGGATACATGCAT[A/G]TATCACCGTGCCTAG | 9169 |
rs577478231 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932053 | TGCATATATATATAT[A/G]TATGTCTGTGTTAAC | 9169 |
rs577504191 | snp | A/C | 0.000399281 | 0.0141238 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993694 | TGAGGCAGGAGAATC[A/C]CTTGAACCTGGGAGG | 9169 |
rs577542353 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45932801 | ATTCAGCGGACAGCA[C/T]GCAGGTAAGACTGGA | 9169 |
rs577622759 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969902 | CACCACATTCAACCA[-/T]TTTTTTTTTTCTTAA | 9169 |
rs577713754 | snp | A/C | 0.00438332 | 0.0466095 | intron-variant | SCAF11 | GRCh38.p7 | 12:45983784 | ACACACACACACACA[A/C]AAAGACTGAACTAAT | 9169 |
rs577727001 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45944661 | AGTCACAAAGAACTA[C/T]GGATGTTGTCATTTT | 9169 |
rs577795883 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45943630 | AACATATCCCCCATG[A/G]ACAAGGGGTAACTAC | 9169 |
rs577820101 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45981231 | GACTAACACAGGATA[C/T]GATTTGTTCGACACC | 9169 |
rs577839478 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990631 | TCCCTGCGCGTCTCC[C/T]TCCTCCTCCCTTCCC | 9169 |
rs577873620 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45930018 | TTTTATGTTATGTGT[C/T]ACATACTGTATTCTT | 9169 |
rs577883108 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45989116 | TTTAGAAACAGACTT[A/G]ATTACATGTCAAAAT | 9169 |
rs577919870 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929229 | CTGGAGCAATCATCG[C/T]GCACAGAAGCCTCAA | 9169 |
rs577943759 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45988182 | AGGTAAGTCAAGGTA[A/C]AATTTACATCTTAAA | 9169 |
rs577974467 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966745 | TTCAAGGAACAACAA[C/T]AAAGAGATGAATGAC | 9169 |
rs577992915 | snp | A/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920747 | ACCACCTGGTCACCA[A/T]ATTAACACTTCATTC | 9169 |
rs578019089 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974349 | AATTCCTTAAAATGA[A/G]ATAACATTCAAGTAT | 9169 |
rs578027752 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45966241 | AAAGCTTAAGAACAT[C/T]AGCAATTATCTTCAA | 9169 |
rs578080266 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | SCAF11 | GRCh38.p7 | 12:45958220 | AATAAATCCCATTTA[C/G]TTAACCTGTGTGTGT | 9169 |
rs578160608 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | SCAF11 | GRCh38.p7 | 12:45980557 | GACTGAAATTCAGAT[A/C]ATCAGGCTCCCTTAT | 9169 |
rs578192485 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969575 | TTATCAAGATCATTA[C/T]TATTCTTATTGTCAG | 9169 |
rs578193796 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | SCAF11 | GRCh38.p7 | 12:45972094 | CAAGCAGCATACCAC[C/T]GACTCTGAAAACTGA | 9169 |
rs745360117 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925831 | AAATTAAAAGTGTAC[A/G]TATCTGAAATAAACA | 9169 |
rs745370949 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943039 | TGAGTATGAATCTAG[A/T]ATTTAAACCTGAATA | 9169 |
rs745385411 | snp | A/G | 1.66471e-05 | 0.00288501 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951638 | TTCATGTTGCAGAAT[A/G]AAAAGACTTACCTTA | 9169 |
rs745452147 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991328 | CCAGCGCTTTGGGAG[A/G]CCGAGGCTGGCGGAT | 9169 |
rs745460857 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45925039 | GTAGCTGAGAACCAT[C/T]AACTTGCTGGTTTGT | 9169 |
rs745473533 | in-del | -/GTTT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45944359 | TTTCAAAGGCAGAAC[-/GTTT]GTTAATCTGTAAATC | 9169 |
rs745473685 | snp | C/T | 1.65949e-05 | 0.00288048 | missense | SCAF11 | GRCh38.p7 | 12:45951709 | AAGGTTTACGGTCAA[C/T]AGGACATGAAGCCAG | 9169 |
rs745475488 | snp | C/T | 0.000115316 | 0.00759243 | missense | SCAF11 | GRCh38.p7 | 12:45928724 | GTTTCAGCTCTTGTG[C/T]TACGTGTAGACCTCC | 9169 |
rs745490093 | snp | A/G | 1.64754e-05 | 0.00287009 | missense | SCAF11 | GRCh38.p7 | 12:45924967 | TATTCATAGGCTGGT[A/G]TTGTGCATTCATTTG | 9169 |
rs745494566 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972676 | ACAAAGTTTTGTAAC[A/G]TAATATTCAAAATGT | 9169 |
rs745532070 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985539 | CCAGCTATAGATACT[C/T]AGCAACTTCTCTGAC | 9169 |
rs745618511 | snp | A/G | 1.64846e-05 | 0.0028709 | missense | SCAF11 | GRCh38.p7 | 12:45928797 | TATTTGATGTACCAG[A/G]AGTTTGCTTCTTTTC | 9169 |
rs745629864 | in-del | -/A | 0.0654984 | 0.168698 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928872 | TACCTAATAATATTT[-/A]AAAAAAAAAAAAAAG | 9169 |
rs745641481 | snp | A/G | 1.65241e-05 | 0.00287433 | missense | SCAF11 | GRCh38.p7 | 12:45927641 | GGATGTTCGGTCAGC[A/G]ATTCATTCTTTTCTT | 9169 |
rs745648943 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991316 | ACGCCGGTAATCCCA[A/G]CGCTTTGGGAGGCCG | 9169 |
rs745690320 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950069 | TACATACATACCCAC[A/G]AGAGAAGGATGTTTT | 9169 |
rs745704643 | snp | C/T | 1.65614e-05 | 0.00287757 | missense | SCAF11 | GRCh38.p7 | 12:45927750 | CTTCATTCCCAAAAG[C/T]ATCACATGTTGCAAT | 9169 |
rs745719108 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934982 | ATAAATTACCATTTA[G/T]CCACTGGCACCCACT | 9169 |
rs745729924 | snp | C/T | 1.65162e-05 | 0.00287365 | missense | SCAF11 | GRCh38.p7 | 12:45926628 | AGTTTATTTTTTCTG[C/T]TATCCAATTGGGACA | 9169 |
rs745757249 | in-del | -/AA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941061 | ATTCTGCCTGAACTC[-/AA]GAGTGAGAAAAGAAA | 9169 |
rs745774267 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948294 | TCAGATTTCAGCTAG[A/T]CCCTCCTTAAATTAT | 9169 |
rs745805554 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963969 | AGAAAAAAATGTGTA[C/T]ACTTAGGCAGCTTAT | 9169 |
rs745839369 | snp | A/G | 0.00010735 | 0.00732553 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934396 | TTTATGGACTAAATA[A/G]CCCTAAAGTGTTATC | 9169 |
rs745841185 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934895 | TCTTTTCCAGCTATC[-/A]ATCTAGAAAACAGGT | 9169 |
rs745846976 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989669 | GATTAGGCTAAATTT[A/G]TATCTCCCGGCCCCG | 9169 |
rs745860612 | in-del | -/AGG | 1.68852e-05 | 0.00290557 | cds-indel | SCAF11 | GRCh38.p7 | 12:45948465 | TAGAATTTTCATGAC[-/AGG]AGACCTGTTTCTCAA | 9169 |
rs745870259 | snp | C/T | 0.000162562 | 0.00901413 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45992000 | CCCGGGATGAGTTTC[C/T]TCCCCACTTTGCCGC | 9169 |
rs745925215 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965206 | TAAAAAAGATAGATA[A/C]GCCAGCCAAGTATGG | 9169 |
rs745949828 | snp | A/G | 1.64808e-05 | 0.00287057 | missense | SCAF11 | GRCh38.p7 | 12:45928574 | CTTCCTCTTCTTACA[A/G]ACTTCCGTTTTGGAG | 9169 |
rs745957924 | snp | A/C/G | 3.29664e-05 | 0.00405984 | missense | SCAF11 | GRCh38.p7 | 12:45928472 | GTGTCAGATTCTGCT[A/C/G]TTTCTTCATCTACTG | 9169 |
rs745964339 | snp | A/G | 0.000263578 | 0.0114769 | missense | SCAF11 | GRCh38.p7 | 12:45927389 | CTTTCAGATGGTTGA[A/G]AAACAGTTTCAACCT | 9169 |
rs746004034 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976394 | ATTGTTCTATTATTT[A/G]TTATTGTTAATCTTT | 9169 |
rs746004052 | snp | A/C | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962506 | CTCCTTAGGATTTGT[A/C]CTACTTTAAACTCCC | 9169 |
rs746034132 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940962 | GGTGTGTATCACCAC[A/C]CTTGGCTAATTTTTG | 9169 |
rs746045222 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989503 | TTCAAAATTCAACAT[G/T]TGAATCCGTGAATGT | 9169 |
rs746052420 | snp | A/G | 3.29576e-05 | 0.00405928 | missense | SCAF11 | GRCh38.p7 | 12:45927459 | AACAGTGTGTCACAG[A/G]ATTTTCATTCATTTG | 9169 |
rs746057115 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975495 | GCTGCTTCGCCTTGC[A/G]CTTTTATGTTATGGA | 9169 |
rs746123587 | snp | C/T | 1.66768e-05 | 0.00288758 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961834 | ACAGACCAGTGGAAA[C/T]AGTATTATCTCCGTT | 9169 |
rs746200797 | snp | C/G | 1.64857e-05 | 0.00287099 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922077 | TTTCAGTAGACACAG[C/G]TTCTTCCAGAGTTTT | 9169 |
rs746212475 | snp | A/C/T | 3.29616e-05 | 0.00405954 | missense | SCAF11 | GRCh38.p7 | 12:45926367 | ACTTGAAAGATTCAC[A/C/T]CCCTGAACTGTTTGA | 9169 |
rs746229913 | snp | C/T | 2.62657e-05 | 0.00362383 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931662 | GTTTAAAAAATTAAA[C/T]CACCAATTTAAAAGT | 9169 |
rs746230620 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956181 | CACATAGGCTGCTTA[G/T]AGATAGCTCCTCTTA | 9169 |
rs746238498 | snp | C/T | 1.65831e-05 | 0.00287945 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964085 | CTTTCAACAAACAAA[C/T]TTTATAAAAATGAAA | 9169 |
rs746244156 | snp | C/T | 3.29946e-05 | 0.00406155 | missense | SCAF11 | GRCh38.p7 | 12:45928026 | CAGGTTGGTACACTT[C/T]GCTTTCAGATGTTAA | 9169 |
rs746281445 | snp | G/T | 6.59261e-05 | 0.00574097 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922414 | TCATTTATTAAAACA[G/T]AGGTGGTTCAAAACA | 9169 |
rs746284042 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954505 | GAGGGGTTAATGGCG[C/T]GAGCTGCTGTACCCA | 9169 |
rs746295593 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969069 | CTAAATTTTAAATTT[C/T]TGTGAAGTTTTAGTT | 9169 |
rs746322617 | snp | C/G | 1.66319e-05 | 0.00288369 | missense | SCAF11 | GRCh38.p7 | 12:45922567 | CTTGTGCTGCTTTTT[C/G]TTGAATTTGCAATTT | 9169 |
rs746334094 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | SCAF11 | GRCh38.p7 | 12:45928116 | GTGAAAGTCCAGATA[C/T]CTGGTCTTGCTTTTC | 9169 |
rs746372347 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981539 | GGAATAAATATAATC[C/T]GTCATCCTTGAATAA | 9169 |
rs746466493 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920827 | TTAGATAAACAACAA[C/T]TTTACGCCAGTGCCA | 9169 |
rs746470257 | snp | A/C | 1.65105e-05 | 0.00287315 | missense | SCAF11 | GRCh38.p7 | 12:45928008 | CACTTAGGGGACAAG[A/C]TACAGGTTGGTACAC | 9169 |
rs746547093 | snp | A/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919703 | AATCAAGTAGCTATT[A/T]ATGCAGTCTAACCAG | 9169 |
rs746564938 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970480 | CCCTACTATGGATGA[G/T]CACTGATATGATAAA | 9169 |
rs746587766 | snp | G/T | 1.64825e-05 | 0.00287071 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928096 | ATCTGTCTTTACCTC[G/T]GATTGTGAAAGTCCA | 9169 |
rs746602262 | snp | A/C | 1.64947e-05 | 0.00287177 | missense | SCAF11 | GRCh38.p7 | 12:45927069 | GGGACAGTGATTCAG[A/C]TCTTCTGCTTTCCCT | 9169 |
rs746610729 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934766 | TATGTTTACAACATA[C/T]GAGTTAAAATTCTAA | 9169 |
rs746618263 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969570 | GGCTGTTATCAAGAT[A/C]ATTATTATTCTTATT | 9169 |
rs746625362 | snp | G/T | 1.69804e-05 | 0.00291374 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924740 | TACCTGCAATTGCTT[G/T]CCATCTGGTTGTGAA | 9169 |
rs746634703 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984043 | AACTTTAAAAGAACA[C/T]GTCTGTATGCTGCTA | 9169 |
rs746656639 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983041 | GGGGGAGTAACTAAC[A/G]ACTGAGGCAAGTAAA | 9169 |
rs746680335 | snp | C/T | 3.29674e-05 | 0.00405988 | missense | SCAF11 | GRCh38.p7 | 12:45924855 | TGCATGAGGGGCACT[C/T]CTGTGTGGAGATGCA | 9169 |
rs746728774 | snp | C/T | 1.691e-05 | 0.0029077 | missense | SCAF11 | GRCh38.p7 | 12:45948473 | TCATGACAGGAGACC[C/T]GTTTCTCAAATGAGT | 9169 |
rs746782796 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959673 | CTTTGAAACATATCT[A/G]TTTTTATCACAGCAA | 9169 |
rs746790592 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933396 | TTCAAAATAAACTCA[C/T]TCCTAAAATAAGTAC | 9169 |
rs746798137 | snp | C/T | 1.64779e-05 | 0.00287031 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928618 | CTTTTCTGACTCAGC[C/T]GAAGAGGGAACACTT | 9169 |
rs746816075 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927496 | ATCAGCATTTACAGA[C/T]GGTTCAACTTCAGAT | 9169 |
rs746830143 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963706 | TGGAACTATAACCTA[C/T]ACATTGAGATTAGGA | 9169 |
rs746843817 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947125 | TTAGTATTCTGATGA[A/G]AAGTACTAATGAATC | 9169 |
rs746870694 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963780 | TGAAAATTAAATTAG[C/G]TTTAGAAGCAGAGGA | 9169 |
rs746889106 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991929 | TCACACGTTTTCCTG[C/T]CGCCTGCCCCCGTTC | 9169 |
rs746901923 | snp | C/T | 0.000164989 | 0.00908116 | missense | SCAF11 | GRCh38.p7 | 12:45927633 | TAGATCTAGGATGTT[C/T]GGTCAGCGATTCATT | 9169 |
rs746913159 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962182 | AATAAGTAACAACTG[C/T]TAAATTTCTTTTGTG | 9169 |
rs746970428 | snp | C/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975439 | CAATGATGTTAGCTA[C/G]GTCTTCTGGATAACC | 9169 |
rs746992379 | snp | C/G | 2.2569e-05 | 0.00335917 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964123 | TTCCATGTCTTCATA[C/G]TTCTTATCTCCCATA | 9169 |
rs747063519 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970271 | TCCAGACCTCAAGCA[A/G]TCTTCCCACCTTGGT | 9169 |
rs747101824 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939651 | TGCAGTGAGCCGAGA[C/T]CGTGCCATTGAGATC | 9169 |
rs747105397 | snp | A/T | 1.72627e-05 | 0.00293786 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934554 | GTATTAATTTTTATT[A/T]AAAAGGCTGTAAACC | 9169 |
rs747145208 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938881 | TGAAAGGGAGATCCT[A/G]TCTGTAAACTATATC | 9169 |
rs747152854 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954126 | ATTTGTATCAGATGC[A/G]TCAAATCTTTCAAAG | 9169 |
rs747157461 | snp | C/T | 1.64885e-05 | 0.00287123 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923115 | CAGGCAAAACTGGTG[C/T]ACTCATGTTATTACT | 9169 |
rs747191004 | snp | G/T | 1.64836e-05 | 0.0028708 | missense | SCAF11 | GRCh38.p7 | 12:45927294 | GAGTGTCTTTGTTGG[G/T]TGACCAAGTTGTAGA | 9169 |
rs747204605 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987339 | TTTATGCTACAGACT[A/G]AGACTTGCTTAGTCT | 9169 |
rs747209601 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938711 | GAAAACATCCTTTTG[C/T]ACGATACAAACAAGT | 9169 |
rs747210229 | in-del | -/AAA | 0.000271952 | 0.0116577 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928872 | TACCTAATAATATTT[-/AAA]AAAAAAAAAAAAGTA | 9169 |
rs747214034 | in-del | -/A | 3.37291e-05 | 0.00410651 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951757 | ACAAATTATATCTTT[-/A]CAAATGTTTCTTTAG | 9169 |
rs747237648 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967998 | TAGTCCTAGCCAGTA[A/C]TTTGTGGTCAATAGC | 9169 |
rs747266262 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967701 | AAGTTTTAGAAGTTG[C/T]ATGCTTTATTCCTTA | 9169 |
rs747303068 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945536 | TGTATTATCTCAGTC[-/T]TTTTTTTTTTTTTTT | 9169 |
rs747312271 | snp | A/C | 6.31532e-05 | 0.00561895 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925104 | AAAGCTTGTGAAAAA[A/C]ATCATGTTATAAATC | 9169 |
rs747348299 | snp | C/T | 8.2373e-05 | 0.00641714 | missense | SCAF11 | GRCh38.p7 | 12:45927377 | GTATCTTTTGGGCTT[C/T]CAGATGGTTGAGAAA | 9169 |
rs747373282 | in-del | -/ATT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982313 | TAAATTTTTTGAGTC[-/ATT]AATATTTATTCCCCA | 9169 |
rs747380226 | snp | A/G | 3.32762e-05 | 0.00407885 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961827 | CTGTACAACAGACCA[A/G]TGGAAATAGTATTAT | 9169 |
rs747408343 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984389 | GTACACTATTTGACA[A/G]TAATTATGATGTGTT | 9169 |
rs747411137 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931025 | CACAATTGATCTTTA[A/G]AACTTATTCTATCCA | 9169 |
rs747421917 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966878 | TCATTATCCTAAATA[C/T]CTGAGAATAAAAAAA | 9169 |
rs747462039 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945165 | TTTCCAGCCTGAAGT[A/G]TTACTGATGAGAACT | 9169 |
rs747466177 | snp | C/G | 2.27069e-05 | 0.00336941 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931646 | CATTTTTGTTTAAAT[C/G]GTTTAAAAAATTAAA | 9169 |
rs747470862 | snp | A/C | 4.98029e-05 | 0.00498988 | missense | SCAF11 | GRCh38.p7 | 12:45926173 | CTCCTCTTGTTTCAT[A/C]CATCCAGACTGTGGA | 9169 |
rs747475330 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980469 | ATGATCTTGAGAGAT[C/T]AACTTCATTTTACAG | 9169 |
rs747479909 | snp | C/T | 1.86722e-05 | 0.00305545 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922225 | TGGGGGGTAAACTTT[C/T]TTCATGCTTAAAGGG | 9169 |
rs747486120 | snp | A/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993303 | CACTTAAAATATCAG[A/T]CCTGTCACATAGCAA | 9169 |
rs747491501 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946623 | CAAGAGCCAAGAGAA[C/T]TGGGTAATTTTGAGG | 9169 |
rs747498531 | in-del | -/TTTGT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969745 | GTGTGAGTGTGTGTG[-/TTTGT]TTTAAGAGAAACAGT | 9169 |
rs747503732 | snp | C/T | 1.66294e-05 | 0.00288347 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922042 | TCCTTGACAGCGTTC[C/T]CCATTTCAGCCTATG | 9169 |
rs747526758 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978497 | ATGCCTATTAGTGAC[A/G]AAAAGCAAAAGAGCA | 9169 |
rs747682926 | in-del | -/CCACGGTTGCCTCTGCCTCTA | 1.65111e-05 | 0.0028732 | cds-indel | SCAF11 | GRCh38.p7 | 12:45926465 | CTGTAAGTGCCTCTG[-/CCACGGTTGCCTCTGCCTCTA]CCACGGTTAGATACC | 9169 |
rs747696151 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932070 | ATGTCTGTGTTAACC[A/G]CCACCCCAATCAAGA | 9169 |
rs747721903 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933317 | CAAAGAATAGCAGTC[A/G]TTTTTGTACCTGGCA | 9169 |
rs747723138 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982746 | TTGTAGACTGTTTCA[C/T]TGATCCCAGAGAATT | 9169 |
rs747729493 | snp | C/T | 3.35154e-05 | 0.00409348 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922034 | TGATAATGTCCTTGA[C/T]AGCGTTCCCCATTTC | 9169 |
rs747740724 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946915 | AAATCATATACAAAG[G/T]TTTATGTCTGTAAAC | 9169 |
rs747756394 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968358 | CTGTGACCCCTAATA[C/T]AATGATCTAACATAC | 9169 |
rs747916591 | snp | C/T | 3.29826e-05 | 0.00406082 | missense | SCAF11 | GRCh38.p7 | 12:45926943 | TCTCTCTCCTCTGCC[C/T]ATCTCTATCACTTTC | 9169 |
rs747929661 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962035 | CAACATTTACTTTCT[C/T]AAATTTTTTTAACGG | 9169 |
rs747933694 | snp | A/G | 1.75949e-05 | 0.002966 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924724 | TGAGTTGCTAAAAAC[A/G]TACCTGCAATTGCTT | 9169 |
rs747944773 | snp | A/C | 1.67091e-05 | 0.00289038 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945337 | ATCAATAAAGACAGG[A/C]AAGAATTAAGAAAAA | 9169 |
rs747961171 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | SCAF11 | GRCh38.p7 | 12:45928494 | CATCTACTGAATCAT[C/T]GGAAGATGATTTTTC | 9169 |
rs747964852 | snp | G/T | 1.6896e-05 | 0.0029065 | missense | SCAF11 | GRCh38.p7 | 12:45948455 | ATACAGCTTTTAGAA[G/T]TTTCATGACAGGAGA | 9169 |
rs748028633 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939603 | CTTGGGAGGCTGAGA[C/G]AGAAGAATTGTTTGA | 9169 |
rs748042968 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45922479 | TTATCTACTGCTTTC[C/T]GTACAATTTCTTTAT | 9169 |
rs748054782 | snp | A/C/G | 3.29588e-05 | 0.00405938 | missense | SCAF11 | GRCh38.p7 | 12:45928595 | CGTTTTGGAGCCTGT[A/C/G]TTGTTTGCTTTTCTG | 9169 |
rs748088470 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973515 | GACAGAATAATCCCA[A/G]TGAAATCCATGCCTG | 9169 |
rs748134984 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987130 | CTTTGGGAGGCCAAG[A/G]CGGGATGATTACTTA | 9169 |
rs748193089 | in-del | -/T | 0.000267738 | 0.0115671 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961287 | TCCACAAGGCTGATA[-/T]TAAAGAAGAAATCAA | 9169 |
rs748213664 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952379 | ATAATATGAATAAGA[A/G]TTTTTTACTTTACAT | 9169 |
rs748222666 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938544 | CTTTCATTCCTTTAT[A/T]GTCATTTTAGTAGAG | 9169 |
rs748237176 | snp | C/T | 1.65293e-05 | 0.00287479 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926533 | TTTATTCCAAGAATT[C/T]CCTGAATTTTCATTT | 9169 |
rs748271125 | snp | A/C | 1.64882e-05 | 0.00287121 | missense | SCAF11 | GRCh38.p7 | 12:45928260 | CTAGCACAGGAAGAT[A/C]TTGAGCACAAGACTC | 9169 |
rs748300627 | snp | A/G | 1.64792e-05 | 0.00287042 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922618 | AATTTATTATTTGCC[A/G]GTCATACTGCTCTCA | 9169 |
rs748302496 | snp | C/T | 1.65192e-05 | 0.00287391 | missense | SCAF11 | GRCh38.p7 | 12:45926624 | CCAGAGTTTATTTTT[C/T]CTGTTATCCAATTGG | 9169 |
rs748317551 | snp | C/T | 1.69387e-05 | 0.00291016 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934519 | TCCTGTACAAAGACA[C/T]AAAAGGACTTGGTTA | 9169 |
rs748403003 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965686 | TGTCCAAATATGCAT[G/T]TATATCTACGCACAA | 9169 |
rs748414517 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939611 | GCTGAGACAGAAGAA[C/T]TGTTTGAACCCAGGA | 9169 |
rs748491705 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920610 | GTATTAAAAAGAGAA[A/G]AAAAAAAAAACCCAA | 9169 |
rs748499196 | snp | A/G | 0.000115305 | 0.00759205 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45923023 | AGCATTAGAGGCTTT[A/G]CTGTGACTTGATGAC | 9169 |
rs748511492 | snp | C/T | 1.64817e-05 | 0.00287064 | missense | SCAF11 | GRCh38.p7 | 12:45928341 | TCTCACTTTCTTCTA[C/T]TTGCTCATTGCAACT | 9169 |
rs748519420 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929341 | TTTTGTATTTTTAAT[A/G]GAGACAGGGTTTTGC | 9169 |
rs748541164 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942025 | TGAACAGTAAATGTA[C/T]TTTCTCATCCTTATG | 9169 |
rs748567044 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978092 | ATGAGTGCCTTTTAT[A/G]TGCCTGGATAGTTTA | 9169 |
rs748568991 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968348 | CTTTTTAGTCTGTGA[-/C]CCCCTAATATAATGA | 9169 |
rs748598691 | snp | A/G | 1.96655e-05 | 0.00313566 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925091 | TATCAAAAGAAAAAA[A/G]GCTTGTGAAAAAAAT | 9169 |
rs748603124 | snp | C/T | 4.95176e-05 | 0.00497558 | missense | SCAF11 | GRCh38.p7 | 12:45927273 | GGGGCCGCTTCTTTT[C/T]TTGTGGAGTGTCTTT | 9169 |
rs748626145 | snp | C/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991087 | CGCATGTTTGCGGTG[C/G]ATTGAGTGTTCACCT | 9169 |
rs748686493 | snp | C/T | 1.70423e-05 | 0.00291905 | missense | SCAF11 | GRCh38.p7 | 12:45926147 | AATACATTACCCTGT[C/T]CAGATGTTTCCTCCT | 9169 |
rs748742283 | snp | A/T | 1.65059e-05 | 0.00287275 | missense | SCAF11 | GRCh38.p7 | 12:45928820 | TTCTTTTCTTCCCCT[A/T]CTTGAGTATGTGCTA | 9169 |
rs748792649 | snp | C/T | 1.64751e-05 | 0.00287007 | missense | SCAF11 | GRCh38.p7 | 12:45924979 | GGTGTTGTGCATTCA[C/T]TTGTTGCTGCATTAC | 9169 |
rs748794943 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931489 | TTTAAAATAGAAAAT[G/T]ATTTCACAAACTTTA | 9169 |
rs748802133 | snp | G/T | 0.000197971 | 0.00994717 | missense | SCAF11 | GRCh38.p7 | 12:45928811 | GAAGTTTGCTTCTTT[G/T]CTTCCCCTTCTTGAG | 9169 |
rs748846116 | snp | A/G | 1.87033e-05 | 0.00305799 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925085 | AGAATCTATCAAAAG[A/G]AAAAAAGCTTGTGAA | 9169 |
rs748862428 | in-del | -/TTTAT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923661 | ACTGTCAGGATTCTA[-/TTTAT]TTTATTTTATTTTAT | 9169 |
rs748890162 | snp | C/T | 0.000100437 | 0.00708579 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931463 | ACTGGAAGAAACTAA[C/T]AATAATAATTTTTAA | 9169 |
rs748893705 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980596 | CCATTGACACTAAAC[C/G]GCCTAATACACAAAA | 9169 |
rs748966791 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953763 | CTTTTTAATAAACTC[A/G]AGCAAGTTACAGTCT | 9169 |
rs749012969 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938713 | AAACATCCTTTTGTA[C/T]GATACAAACAAGTAT | 9169 |
rs749055457 | snp | A/G | 1.65806e-05 | 0.00287924 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927862 | AATTTCACCCTCAGA[A/G]GATTCTAACTTGGGG | 9169 |
rs749082226 | snp | G/T | 0.000332613 | 0.0128917 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45992036 | CGCCGACCGACCGCT[G/T]CACTGCCGCCTTCCT | 9169 |
rs749082460 | snp | A/C | 1.6495e-05 | 0.0028718 | missense | SCAF11 | GRCh38.p7 | 12:45926653 | GGGACAGTCATTTCT[A/C]TGTTTGTCAGCAGAA | 9169 |
rs749097910 | snp | C/T | 1.64743e-05 | 0.00287 | missense | SCAF11 | GRCh38.p7 | 12:45926787 | ATCTCCAACCATCAT[C/T]TGCCCATCTTCCCTT | 9169 |
rs749120207 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930701 | ATGACTGCAAATGGT[A/G]GAACCATGTGGTTTG | 9169 |
rs749130513 | snp | C/G | 6.5925e-05 | 0.00574092 | missense | SCAF11 | GRCh38.p7 | 12:45928378 | GCAATTAGCAGACTG[C/G]TTTTCTACATGAGTC | 9169 |
rs749131538 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921075 | GCAATCCCCGCCTCC[C/T]GGGTTCAACTGATTC | 9169 |
rs749138636 | snp | C/T | 1.64944e-05 | 0.00287175 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923124 | CTGGTGTACTCATGT[C/T]ATTACTTACATGAGA | 9169 |
rs749189452 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985898 | TTCTTACCTTATTAA[C/G]CTCTTATCAACACTT | 9169 |
rs749200425 | snp | C/G | 1.6625e-05 | 0.00288309 | missense | SCAF11 | GRCh38.p7 | 12:45945306 | CTTCTCTTACGATGG[C/G]TTTTCTTCTGTAAAC | 9169 |
rs749202251 | in-del | -/CTT | 1.64879e-05 | 0.00287118 | cds-indel | SCAF11 | GRCh38.p7 | 12:45928804 | TGTACCAGAAGTTTG[-/CTT]CTTTTCTTCCCCTTC | 9169 |
rs749259919 | snp | A/G | 1.83619e-05 | 0.00302996 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924700 | TACAATGGCTATATT[A/G]ATTAAACTTGAGTTG | 9169 |
rs749292193 | in-del | -/TC | 0.000115595 | 0.00760157 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45926924 | TTTCTGGTTCTCCTT[-/TC]TCTCTCTCTCCTCTG | 9169 |
rs749308119 | snp | C/T | 6.72179e-05 | 0.00579693 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961846 | AAATAGTATTATCTC[C/T]GTTTTCTTCACCTGT | 9169 |
rs749311858 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920584 | CCTTTTATAAAAACT[A/G]AGATATTCTAGTATT | 9169 |
rs749349625 | in-del | -/TAGA | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991616 | CCTCCGCGTTGTGGT[-/TAGA]TAGTGACGTGTGTGC | 9169 |
rs749357154 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927466 | TGTCACAGAATTTTC[A/G]TTCATTTGTTTAAGA | 9169 |
rs749388051 | snp | A/G | 3.29582e-05 | 0.00405931 | missense | SCAF11 | GRCh38.p7 | 12:45927596 | TTCTGAATCTGTTCA[A/G]TGTGTGTTTTAGGCA | 9169 |
rs749401649 | snp | A/G | 2.64687e-05 | 0.00363781 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964099 | ACTTTATAAAAATGA[A/G]AAGTTACCTTCCATG | 9169 |
rs749404676 | snp | A/C | 1.65214e-05 | 0.0028741 | missense | SCAF11 | GRCh38.p7 | 12:45926505 | GGTTAGATACCCAAC[A/C]AGAACCAAAGTTTTT | 9169 |
rs749435247 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977834 | AGTTCTGAGAGACAA[C/G]AGATATCTATAACCT | 9169 |
rs749450277 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980873 | GTGTTTGGGAGGAGT[C/G]TTCCTCCTCCCAAAA | 9169 |
rs749470820 | snp | A/T | 1.64792e-05 | 0.00287042 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922427 | CAGAGGTGGTTCAAA[A/T]CAACGTGCACATACT | 9169 |
rs749482153 | snp | G/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990948 | GGCCTCTGCCCTCCT[G/T]TGGCAGTTTTACAGG | 9169 |
rs749500413 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945012 | ATTGTGAAACACTCT[G/T]TTCTCCCAACACACG | 9169 |
rs749523306 | snp | C/T | 1.74747e-05 | 0.00295585 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933254 | GATAAATTTTAGACC[C/T]TCATCAGAATCTCAC | 9169 |
rs749525971 | snp | A/T | 1.70697e-05 | 0.00292139 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922602 | TGAGAAGAAAATGTA[A/T]AATTTATTATTTGCC | 9169 |
rs749542781 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976765 | GAAAAGGTCTCAAAT[C/G]AGTAATTTAAACTTG | 9169 |
rs749650524 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941893 | GCCTCTCCTGCCTCC[C/T]CTTCCACCTTTTCTG | 9169 |
rs749660550 | snp | C/T | 1.91742e-05 | 0.00309624 | missense | SCAF11 | GRCh38.p7 | 12:45934272 | TGATTTGTACTCCAA[C/T]TTGATCTCTGAGGCT | 9169 |
rs749686159 | snp | A/C | 1.64963e-05 | 0.00287192 | missense | SCAF11 | GRCh38.p7 | 12:45927107 | TCCCTTTTTGGAGAC[A/C]GAGACTGAGATTGCC | 9169 |
rs749724038 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989793 | GCGCCGGCTCTTCCC[C/T]ATTCGCGCACTCGAG | 9169 |
rs749733516 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988518 | AAAGGACGATAGAGA[A/G]CTAAGTAACTCCTGA | 9169 |
rs749820742 | snp | A/C | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919606 | AGAATGAGGAATATT[A/C]AAGCAATGTATTTTT | 9169 |
rs749821595 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972360 | GTCAAGATGGGAGGA[C/G]TGCTTAAAGCTAGTA | 9169 |
rs749842070 | snp | C/G | 1.66208e-05 | 0.00288273 | missense | SCAF11 | GRCh38.p7 | 12:45951650 | AATAAAAAGACTTAC[C/G]TTAACATAACCTTCC | 9169 |
rs749869544 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963327 | TAAAATATCAAAGAC[A/G]AAACCAAGACCTTAA | 9169 |
rs749876272 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988269 | CTACAGTTGACTTTC[-/T]TTTTATTACTTTTAT | 9169 |
rs749897990 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959912 | GTTTAAACACTATCA[A/C]AACTCCTCCCTGCCT | 9169 |
rs749903779 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923352 | CGGGGCCTTATTTAG[A/C]TATGTCAAGATGACT | 9169 |
rs749917640 | snp | C/T | 1.68459e-05 | 0.00290219 | missense | SCAF11 | GRCh38.p7 | 12:45934469 | ATCTTTATTGCTGCA[C/T]TTTTCTTTCCTCCTG | 9169 |
rs749927651 | in-del | -/AA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963880 | CAGTAGAGAGTAAAC[-/AA]CTTTAAGAAAAAAGG | 9169 |
rs749951539 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45974005 | ATAAGATTTCCAATA[C/T]AGGCATATATACCTC | 9169 |
rs749966940 | snp | G/T | | | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922167 | CCACTTTAGTAGAAT[G/T]TACTTCTCCACTCTT | 9169 |
rs749967873 | snp | A/G | 1.65184e-05 | 0.00287384 | missense | SCAF11 | GRCh38.p7 | 12:45928830 | CCCCTTCTTGAGTAT[A/G]TGCTAATGCATATCC | 9169 |
rs749979766 | snp | C/T | 1.65075e-05 | 0.00287289 | missense | SCAF11 | GRCh38.p7 | 12:45927257 | CTGGGAGATGGAGAC[C/T]GGGGCCGCTTCTTTT | 9169 |
rs749981627 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987628 | TATACACAGTAGTTA[C/G]AGAAGACCACAACAG | 9169 |
rs749993569 | snp | C/T | 1.64727e-05 | 0.00286986 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45923074 | TCCCTGAACCATTCC[C/T]GTATTTCCTGGGGCT | 9169 |
rs749999265 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925374 | CCTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC | 9169 |
rs750025946 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938166 | CTCTCCAGCTTTCTT[A/G]TCTTTGTGGCTTAAA | 9169 |
rs750036534 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986743 | GGGCAGTTTCCCCCA[C/T]ACTGTTCTCATGGTA | 9169 |
rs750053704 | snp | A/G | 1.69106e-05 | 0.00290775 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45925066 | TTGTTTGGTCTTTTA[A/G]GCTAGAATCTATCAA | 9169 |
rs750131430 | in-del | -/AA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972587 | AAACCCTGTCTCTTA[-/AA]AAAAAAAAAAAAAAA | 9169 |
rs750233140 | snp | C/T | 1.66114e-05 | 0.00288192 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961743 | CAGAAGACATGATTA[C/T]AGCTTTCTGGAAAAC | 9169 |
rs750244464 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930192 | AGCTATAGATCTCAA[C/T]CTGTTCCTATCAAGG | 9169 |
rs750275127 | snp | C/T | 1.74385e-05 | 0.00295278 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926134 | ATAAACCAACAAGAA[C/T]ACATTACCCTGTCCA | 9169 |
rs750286788 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966285 | TTCTGAAGGGAGGTA[A/G]AATAATCTATCAATG | 9169 |
rs750289520 | snp | C/G | 0.000723529 | 0.0190063 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928898 | AAAAGTAAAAAATAT[C/G]TTTTAAGAAATAGTA | 9169 |
rs750305854 | snp | C/G | 0.000264997 | 0.0115078 | missense | SCAF11 | GRCh38.p7 | 12:45927839 | GATTGTCTGTCCACT[C/G]TCTGTATAATTTCAC | 9169 |
rs750328709 | snp | C/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992059 | GCCTTCCTGCATTCT[C/G]GCAGACTACGTTGCG | 9169 |
rs750340333 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979575 | TCACTTTCTTCATAC[A/T]AATCCCTTACAAATT | 9169 |
rs750391524 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941212 | ATGCAAATATACAAT[G/T]TCTTCAGAGCATCTC | 9169 |
rs750397623 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978584 | CTTGGGTCAACAGCA[C/G]TGTATTTTCACATCT | 9169 |
rs750454369 | in-del | -/GTT | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918842 | GTTTGCTTGGCATTA[-/GTT]ATTACCTTTGGTAGG | 9169 |
rs750478095 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942529 | AATGATCTCCCCTTA[C/T]GTCTTACTCTTTCTC | 9169 |
rs750526320 | snp | C/G | 1.70737e-05 | 0.00292174 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948432 | TTCTAAAGTTAATCA[C/G]TAACCTTATACAGCT | 9169 |
rs750529418 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958507 | GTTGGATCTAACAGT[C/T]ATGGTTTAAATTAAC | 9169 |
rs750534824 | snp | C/T | 1.64882e-05 | 0.00287121 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924818 | TGGTAGTCCCTGAGA[C/T]ACACTGGTAGGAGTG | 9169 |
rs750543741 | in-del | -/TCC | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921309 | TTTTCCAAATCTTTT[-/TCC]TCCTCAAAGTCTTCA | 9169 |
rs750546572 | snp | C/T | 1.97857e-05 | 0.00314523 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948555 | ATGAGAAAAGCAAAA[C/T]CAATTTAGAGCAACA | 9169 |
rs750570809 | snp | G/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990844 | GGGAGGAAGGGCAGC[G/T]GCGCTGGAGGGGCCT | 9169 |
rs750588644 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957775 | CATATACTGCAGGTT[C/T]CATTAAACATTGTTA | 9169 |
rs750597250 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971605 | GAGAGCAAGCTCTAA[C/G]AGAATCCCTCTAAAT | 9169 |
rs750619487 | snp | A/G | 1.64751e-05 | 0.00287007 | missense | SCAF11 | GRCh38.p7 | 12:45928706 | CTCTGAGACTGACTG[A/G]CTGTTTCAGCTCTTG | 9169 |
rs750647537 | in-del | -/ACT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951981 | GCTGCCCGGTTGAGA[-/ACT]ACTAGTATAGTGAAA | 9169 |
rs750720083 | in-del | -/TC | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993067 | GTAAAGATTTATTAT[-/TC]TCTCTGATGTTTTCA | 9169 |
rs750752508 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970187 | GCATGAGCCACCGCG[C/T]CCGGCCTCAACTAAT | 9169 |
rs750758513 | snp | A/T | 3.73783e-05 | 0.00432293 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964204 | CTATAAGATAAATTA[A/T]AATAGAGAATTTTAT | 9169 |
rs750778510 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984068 | CTGCTATTCTGGCTG[A/G]AGGCATTGGAGCCCA | 9169 |
rs750780810 | snp | A/G | 1.64784e-05 | 0.00287035 | missense | SCAF11 | GRCh38.p7 | 12:45927579 | TGTCCTCACTAAAAT[A/G]CTTCTGAATCTGTTC | 9169 |
rs750783536 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935514 | TGGTAGGTACACAGA[C/T]AACACTCTTAGAAAT | 9169 |
rs750797710 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983870 | AAGTCTAGGGTAAAA[G/T]AAAGGATAAAAAAGG | 9169 |
rs750820239 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987072 | CTCTAAAAACACAGA[C/T]CCCTTAGGCTGGGTG | 9169 |
rs750838811 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934558 | TAATTTTTATTAAAA[A/C]GGCTGTAAACCAGCA | 9169 |
rs750855906 | snp | C/T | 4.95389e-05 | 0.00497664 | missense | SCAF11 | GRCh38.p7 | 12:45926471 | GTGCCTCTGCCACGG[C/T]TGCCTCTGCCTCTAC | 9169 |
rs750874144 | snp | C/T | 6.6143e-05 | 0.0057504 | missense | SCAF11 | GRCh38.p7 | 12:45926592 | ACTTTTCTGGATTTC[C/T]GGTTCTTGGATCAGG | 9169 |
rs750899236 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982578 | GGTGTAGTGGTACAC[A/G]CCTGTAATCCTAGCT | 9169 |
rs750912567 | snp | C/T | 1.84647e-05 | 0.00303842 | missense | SCAF11 | GRCh38.p7 | 12:45934233 | ACAGAAGAAAACATA[C/T]TGGAGAAAAAATTTC | 9169 |
rs750930011 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985588 | CTTCTCCAGAGCCCC[A/C]GACTCATTTCTGTAA | 9169 |
rs750951415 | in-del | -/AG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972931 | TATAGATATATAGAT[-/AG]ATATATAGATATATA | 9169 |
rs750956272 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932769 | ATTTTTGAGGAGAGG[A/T]ATATGGTAAAAGCGT | 9169 |
rs750987619 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45933222 | TTTCACTGGCTTCTA[C/T]AAATTCTGTACTAAA | 9169 |
rs751001375 | in-del | -/GTGGA | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991132 | CCTGAAATGCAGCCT[-/GTGGA]GTGAAGAGTCGGCAA | 9169 |
rs751026293 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969113 | CAATGTGCTACTGTA[C/G]AGCTATTTAAAAATA | 9169 |
rs751050381 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937811 | CTGTACCATCATTTA[C/T]GCTAAAGTTTAAATC | 9169 |
rs751078762 | snp | A/C | 1.66663e-05 | 0.00288667 | missense | SCAF11 | GRCh38.p7 | 12:45933193 | ATGTCTCTTCTGCCT[A/C]ATCAATGCACTGATT | 9169 |
rs751080234 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985367 | TTTTTCTCTACTTAG[C/G]CTCTGACATCCTGTC | 9169 |
rs751103549 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936280 | CTGAGCAGCTGGGAC[C/T]ACAGGCGCACACCAC | 9169 |
rs751109177 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971995 | AAAATACCATGGATA[C/T]AACAGAGAGAAAAGA | 9169 |
rs751144855 | snp | A/G | 4.95634e-05 | 0.00497788 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45922526 | ATCTTTATTTTGGTA[A/G]AATGGCTTGATGGCC | 9169 |
rs751147496 | snp | A/C | 1.64885e-05 | 0.00287123 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922924 | GAAGGTTGCTCTCAA[A/C]CTTGAACTTGCCTTG | 9169 |
rs751172549 | snp | A/G | 1.87619e-05 | 0.00306278 | missense | SCAF11 | GRCh38.p7 | 12:45934213 | AAGATTCTCCAGAGT[A/G]GCTAACAGAAGAAAA | 9169 |
rs751184641 | in-del | -/TTCAGA | 4.94376e-05 | 0.00497156 | cds-indel | SCAF11 | GRCh38.p7 | 12:45927505 | TACAGATGGTTCAAC[-/TTCAGA]TTCATTTTGGTCACT | 9169 |
rs751190660 | snp | C/T | 1.64857e-05 | 0.00287099 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927154 | ATCCTTTTTTGGGGA[C/T]TGAGAACGGGATTTT | 9169 |
rs751243360 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | SCAF11 | GRCh38.p7 | 12:45928299 | AAGATCCTACTCTTT[C/T]CTCTGTATCATAATT | 9169 |
rs751339119 | snp | C/T | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928465 | AGGTGATGTGTCAGA[C/T]TCTGCTGTTTCTTCA | 9169 |
rs751380258 | snp | A/T | 1.65899e-05 | 0.00288005 | missense | SCAF11 | GRCh38.p7 | 12:45951698 | CACTGCCTGAAAAGG[A/T]TTACGGTCAATAGGA | 9169 |
rs751406721 | snp | A/G | 1.65051e-05 | 0.00287267 | missense | SCAF11 | GRCh38.p7 | 12:45927248 | GTTTCTCTTCTGGGA[A/G]ATGGAGACTGGGGCC | 9169 |
rs751413150 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976215 | AATATCAATTCTAAG[C/T]AGACTAAAATTTTAA | 9169 |
rs751470158 | snp | A/G | 3.2962e-05 | 0.00405954 | missense | SCAF11 | GRCh38.p7 | 12:45928790 | CCTCTGGTATTTGAT[A/G]TACCAGAAGTTTGCT | 9169 |
rs751479962 | snp | A/T | 3.3222e-05 | 0.00407553 | missense | SCAF11 | GRCh38.p7 | 12:45925054 | CAACTTGCTGGTTTG[A/T]TTGGTCTTTTAGGCT | 9169 |
rs751548597 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989370 | ATTTTTCAGCAGTTT[C/T]GCTTAAGTATCTTAG | 9169 |
rs751602063 | snp | A/G | 1.66095e-05 | 0.00288175 | missense | SCAF11 | GRCh38.p7 | 12:45945287 | ACTTTTGCACTTAAT[A/G]GATCTTCTCTTACGA | 9169 |
rs751602932 | in-del | -/CTC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924235 | CTCACAGAGGCACTT[-/CTC]CTTTCTTTTTAGCAT | 9169 |
rs751678697 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955848 | TAGTCTAATAACATC[A/G]TTGGCTTTATGATAC | 9169 |
rs751733730 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969029 | TCTATCAAGCACTTC[A/C]AGTGTGGACAGTGCA | 9169 |
rs751759931 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | SCAF11 | GRCh38.p7 | 12:45926867 | TTACTTTTTGTTCTA[C/T]ATCTTGAGGGGGACC | 9169 |
rs751764890 | snp | C/T | 1.75277e-05 | 0.00296033 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948409 | TGTTCCACTCATTTG[C/T]ATTCCACTTCTAAAG | 9169 |
rs751778354 | snp | C/T | 1.85817e-05 | 0.00304803 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924683 | ATGAACAGCTAAATG[C/T]TTACAATGGCTATAT | 9169 |
rs751833329 | snp | A/T | 1.65608e-05 | 0.00287752 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924779 | GTTGACTTGTTGGGA[A/T]GGTGGGGGAGGGGGT | 9169 |
rs751898209 | snp | C/T | 8.08767e-05 | 0.0063586 | missense | SCAF11 | GRCh38.p7 | 12:45934188 | AACCAATAAGCTCTA[C/T]AGGTAAAGGAAGATT | 9169 |
rs751898992 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | SCAF11 | GRCh38.p7 | 12:45928566 | GTGGTTTTCTTCCTC[C/T]TCTTACAGACTTCCG | 9169 |
rs751931342 | in-del | -/CAT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989323 | GAGAAAAAAATTTAA[-/CAT]CAGCATCTACTACAC | 9169 |
rs751937766 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955544 | AGATGTTTTTAGTTT[C/T]CAGAGTAAAATTTAC | 9169 |
rs751953166 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947793 | GATATCTCCCTGCCT[C/T]AACTTCCTAAGTAGC | 9169 |
rs752004498 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946496 | AGCTGTTATTTCCTT[A/G]TGACAAATCTCAGAA | 9169 |
rs752006684 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959253 | GCCTGGGTGACAGAC[-/T]TGAGACTCTGTCTCA | 9169 |
rs752050718 | snp | A/C | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961474 | CCTATAAGGTTATTA[A/C]CTTTTTTTAAAAAAG | 9169 |
rs752128114 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987316 | CATGGATATAAGTAA[C/G]TTGGCAGTTTATGCT | 9169 |
rs752134201 | snp | C/G | 1.65091e-05 | 0.00287303 | stop-gained | SCAF11 | GRCh38.p7 | 12:45926452 | GGCAAAACTACTTCT[C/G]TAAGTGCCTCTGCCA | 9169 |
rs752158192 | snp | A/G | 1.71985e-05 | 0.0029324 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961881 | GTAAAACAGCCATAT[A/G]TGCTTTCAAGTTCTC | 9169 |
rs752248430 | snp | C/T | 3.35469e-05 | 0.0040954 | missense | SCAF11 | GRCh38.p7 | 12:45933140 | TTTTACCTTCCAATT[C/T]CAGGTAATGTATCAG | 9169 |
rs752250902 | snp | A/C | 1.65869e-05 | 0.00287979 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961807 | TTGGGCATCTGTCAG[A/C]CTCACTGTACAACAG | 9169 |
rs752267370 | snp | G/T | 2.07846e-05 | 0.00322364 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931636 | ATAATAAAGACATTT[G/T]TGTTTAAATGGTTTA | 9169 |
rs752274981 | snp | A/T | 1.65059e-05 | 0.00287275 | missense | SCAF11 | GRCh38.p7 | 12:45926436 | CATTCTGATCTTTAT[A/T]GGCAAAACTACTTCT | 9169 |
rs752289656 | snp | C/T | 3.29511e-05 | 0.00405887 | missense | SCAF11 | GRCh38.p7 | 12:45926327 | TCCTGTTCACTTTTT[C/T]GCTTATAGGATTGCT | 9169 |
rs752319265 | snp | A/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990889 | TTCCAGCACCGCCCT[A/T]CGCCCACACTGCGGA | 9169 |
rs752332668 | in-del | -/ATTTA | 1.70813e-05 | 0.00292239 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45934450 | GTTTCAACAAACCTT[-/ATTTA]TCTTTATTGCTGCAT | 9169 |
rs752356482 | in-del | -/C | 1.64827e-05 | 0.00287073 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45928478 | ATTCTGCTGTTTCTT[-/C]CATCTACTGAATCAT | 9169 |
rs752376610 | snp | G/T | 1.80497e-05 | 0.00300409 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922213 | AGAAAAAAGGGGTGG[G/T]GGGTAAACTTTTTTC | 9169 |
rs752417670 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966986 | TTCAGATGTAATATA[C/T]TATCCCTTTATGTAA | 9169 |
rs752431624 | snp | A/G | 1.64906e-05 | 0.00287142 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45922493 | CCGTACAATTTCTTT[A/G]TATTCTTCCTTGGTG | 9169 |
rs752465779 | snp | A/G | 1.64833e-05 | 0.00287078 | missense | SCAF11 | GRCh38.p7 | 12:45928085 | ACTGTACATACATCT[A/G]TCTTTACCTCTGATT | 9169 |
rs752507928 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955654 | ATTTTTAAGTTATTT[G/T]AATTTTGAAGAAAAT | 9169 |
rs752510406 | snp | C/T | 2.10029e-05 | 0.00324053 | missense | SCAF11 | GRCh38.p7 | 12:45934183 | ATACTAACCAATAAG[C/T]TCTATAGGTAAAGGA | 9169 |
rs752521395 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941434 | GTGAGAACACAAGAT[C/G]TAAATTTCAAGTGTA | 9169 |
rs752523465 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925759 | AAAACAAGGAAATAT[A/C]AATCTTTACTATTAA | 9169 |
rs752530929 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975913 | ATATCACAACAGATA[C/T]AATAATAACAAAGAT | 9169 |
rs752553978 | snp | A/G | 1.64901e-05 | 0.00287137 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928210 | AGCCTCTATACCTGT[A/G]TTCTCGAGTTTTTTA | 9169 |
rs752555665 | snp | A/G | 0.000148455 | 0.00861425 | missense | SCAF11 | GRCh38.p7 | 12:45927053 | GAAGTTTCTCTTCTT[A/G]GGGACAGTGATTCAG | 9169 |
rs752572001 | snp | G/T | 1.64876e-05 | 0.00287116 | missense | SCAF11 | GRCh38.p7 | 12:45927145 | TCTTGCAATATCCTT[G/T]TTTGGGGACTGAGAA | 9169 |
rs752574671 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940497 | CATTGGATATAGAGT[C/T]AGAAGACTGGATCAA | 9169 |
rs752583297 | snp | A/G | 1.64765e-05 | 0.00287019 | missense | SCAF11 | GRCh38.p7 | 12:45924924 | ATGTTCATCAAAGGA[A/G]CATGAACACCCACTG | 9169 |
rs752588013 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989268 | AATAATGCATTTATT[A/G]ATATGCTTTTCCCAA | 9169 |
rs752606659 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969413 | CCAGTTCACTTCAAA[A/G]CTCCCTCTCCCTCCT | 9169 |
rs752632850 | snp | A/G | 8.24083e-05 | 0.00641852 | missense | SCAF11 | GRCh38.p7 | 12:45924852 | ACCTGCATGAGGGGC[A/G]CTCCTGTGTGGAGAT | 9169 |
rs752716013 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942224 | ATTTCTGACTGTGCA[-/G]GGGTACCCCTAACTC | 9169 |
rs752801858 | snp | C/G | 1.66076e-05 | 0.00288158 | missense | SCAF11 | GRCh38.p7 | 12:45927713 | AGTAAGTTATTTTCA[C/G]AGTCTTGAATATTAT | 9169 |
rs752833115 | in-del | -/ATC | 1.66593e-05 | 0.00288607 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923170 | CTGTTTTAAAGAGTT[-/ATC]ATCAGTTAATGAATT | 9169 |
rs752868652 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981210 | GTCTTCTGCTATGTT[A/C]ACCATGACTAACACA | 9169 |
rs752892524 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45944470 | AAAAATGAAGTTATT[C/T]ACTTTTTAAAACAAT | 9169 |
rs752906064 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926713 | ATTTTTTTCTTTTCT[C/T]GTATTTTCATTCTGT | 9169 |
rs752921576 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993994 | GTGAGACCTAGTTTC[C/T]ACTAAAAATAAAATT | 9169 |
rs752970411 | snp | A/C/G | 4.94428e-05 | 0.00497186 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923104 | TGCTGTCGGAGCAGG[A/C/G]AAAACTGGTGTACTC | 9169 |
rs753024152 | snp | G/T | 4.98492e-05 | 0.00499221 | missense | SCAF11 | GRCh38.p7 | 12:45945255 | GTAACTTACTATGTA[G/T]CCACTTCAAGTCACA | 9169 |
rs753057739 | snp | A/C | 1.64825e-05 | 0.00287071 | missense | SCAF11 | GRCh38.p7 | 12:45928435 | TACATCTGGTTGGTG[A/C]TCTTTTTCTAACACA | 9169 |
rs753062867 | snp | C/T | 0.000115305 | 0.00759205 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923054 | GAAGTATTACCAGAA[C/T]TTGGTCCCTGAACCA | 9169 |
rs753065901 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924345 | TAAAAGCTTCATCAC[A/G]GTACTTAATCACTAG | 9169 |
rs753078309 | snp | A/G | 9.88533e-05 | 0.00702971 | missense | SCAF11 | GRCh38.p7 | 12:45927362 | TTGGTTTTATCTATG[A/G]TATCTTTTGGGCTTT | 9169 |
rs753083892 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958433 | ATAGATGATAAGCTT[C/T]AGCATACTGGCTCTA | 9169 |
rs753196006 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958738 | CTACCACAGGTTCAC[A/C]CTGAAACATTTTGCC | 9169 |
rs753206536 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973744 | CTAAAATCCTCTATC[G/T]AGTGAAAATATCCTT | 9169 |
rs753265704 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955901 | GCTCACTGCTTTACA[A/G]TGTAATGTGTATTAA | 9169 |
rs753268754 | snp | A/G | 1.64798e-05 | 0.00287047 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927442 | CGGCATATTATTTTC[A/G]GAACAGTGTGTCACA | 9169 |
rs753272341 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946860 | CTAACTTTGGGGCTC[A/C]TGGGTAGGCTCTTGG | 9169 |
rs753298787 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925362 | GTTCGAGAGCAGCCT[A/G]GCCAACATGGTGAAA | 9169 |
rs753303362 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921721 | TGCACTTAGAAGTTT[C/T]TAATTTATGCACTCC | 9169 |
rs753307354 | in-del | -/CA | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920786 | GCATTTGGGGATTTT[-/CA]AGTGTGAAAATATTT | 9169 |
rs753369101 | snp | C/T | 6.59261e-05 | 0.00574097 | missense | SCAF11 | GRCh38.p7 | 12:45928422 | TGTTACTACTGTCTA[C/T]ATCTGGTTGGTGCTC | 9169 |
rs753379720 | in-del | -/AATA | 1.66585e-05 | 0.00288599 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945325 | TCTTCTGTAAACATC[-/AATA]AAGACAGGAAAGAAT | 9169 |
rs753382347 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975848 | TATATGGGCGCTCTT[C/T]GTGGTGCCCCAAAAT | 9169 |
rs753395237 | snp | A/G | 0.000121751 | 0.00780132 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956222 | AACAAGTGTTAAGAC[A/G]AGTGCTTAAAGACTA | 9169 |
rs753435473 | snp | A/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975129 | CAGTAAACCATGCTG[A/T]AAACGGATGTGCTGT | 9169 |
rs753436067 | snp | A/G | 3.3661e-05 | 0.00410236 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922026 | AGATATCCTGATAAT[A/G]TCCTTGACAGCGTTC | 9169 |
rs753452250 | in-del | -/GATATATATATATATAGATATATATATA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972865 | ATATATATATATATC[-/GATATATATATATATAGATATATATATA]GATATATATATATAT | 9169 |
rs753467446 | snp | A/G | 1.6476e-05 | 0.00287014 | missense | SCAF11 | GRCh38.p7 | 12:45927359 | TTTTTGGTTTTATCT[A/G]TGGTATCTTTTGGGC | 9169 |
rs753481941 | snp | A/C | 1.64811e-05 | 0.00287059 | missense | SCAF11 | GRCh38.p7 | 12:45927430 | AAGATCAGAAGACGG[A/C]ATATTATTTTCAGAA | 9169 |
rs753483900 | snp | C/T | 1.71997e-05 | 0.0029325 | missense | SCAF11 | GRCh38.p7 | 12:45926142 | ACAAGAATACATTAC[C/T]CTGTCCAGATGTTTC | 9169 |
rs753492304 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980465 | ACTATGATCTTGAGA[-/G]GATTAACTTCATTTT | 9169 |
rs753496745 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987765 | GACTGAGAAGGGAAG[A/C]CATTTGAGAAAAGAA | 9169 |
rs753575847 | snp | A/G | 1.64743e-05 | 0.00287 | missense | SCAF11 | GRCh38.p7 | 12:45926297 | GATCTATCTGCTGGT[A/G]TATCAAATGAGAACT | 9169 |
rs753603355 | snp | A/C | 1.89138e-05 | 0.00307515 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931616 | ATAAAACCAATTCTG[A/C]AAACATAATAAAGAC | 9169 |
rs753608465 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940407 | GGTTGCAGACAACCA[C/T]AAAGTGAGAGGCTTA | 9169 |
rs753645241 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939462 | GCACTTTGGGAGGCC[A/G]AGACGGGCAGATCAT | 9169 |
rs753654649 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974745 | AGTCATCCATGAGGG[C/T]TGGAATCAACTTCTT | 9169 |
rs753657992 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967557 | GGTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 9169 |
rs753686371 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987041 | GATAGTTTCAAGGTC[A/G]CATACTGTTATACTC | 9169 |
rs753696205 | snp | G/T | 1.76378e-05 | 0.00296961 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933109 | CATGTAAACACCTGA[G/T]TAAATAATTTTTTAT | 9169 |
rs753708396 | in-del | -/TT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938027 | GGTATGTGTACTGTC[-/TT]GAGATTCTTAACTCC | 9169 |
rs753708895 | snp | C/T | 1.6483e-05 | 0.00287076 | missense | SCAF11 | GRCh38.p7 | 12:45928076 | GGAAGATGAACTGTA[C/T]ATACATCTGTCTTTA | 9169 |
rs753724763 | snp | A/C | 1.76219e-05 | 0.00296827 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922204 | ACAAACCTAAGAAAA[A/C]AGGGGTGGGGGGTAA | 9169 |
rs753743183 | snp | A/G | 1.64901e-05 | 0.00287137 | missense | SCAF11 | GRCh38.p7 | 12:45926915 | CTAGACCACTTTCTG[A/G]TTCTCCTTTCTCTCT | 9169 |
rs753743903 | snp | C/T | 1.64939e-05 | 0.0028717 | missense | SCAF11 | GRCh38.p7 | 12:45927050 | CTAGAAGTTTCTCTT[C/T]TTGGGGACAGTGATT | 9169 |
rs753851043 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969936 | GGAGTCTCGCTCTGT[-/C]GCCCAGGCTGGAGTG | 9169 |
rs753861104 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980869 | ACCTGTGTTTGGGAG[A/G]AGTGTTCCTCCTCCC | 9169 |
rs753938467 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942715 | TCTTGAAGGTCACTG[C/T]TCAAATATATCTTTA | 9169 |
rs753941182 | snp | A/C | 3.29527e-05 | 0.00405898 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928714 | CTGACTGGCTGTTTC[A/C]GCTCTTGTGTTACGT | 9169 |
rs753972694 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993817 | AAAAAAAGAAAAACA[C/T]GGTTCTAATACTGTC | 9169 |
rs753979039 | snp | C/G | 1.64882e-05 | 0.00287121 | missense | SCAF11 | GRCh38.p7 | 12:45925023 | TGCATCATATTTATA[C/G]GTAGCTGAGAACCAT | 9169 |
rs753996181 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979859 | TAACCCAGATACCGA[C/T]TGTATTACATACTAT | 9169 |
rs754024896 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959483 | AAGGCATGGCCTGTT[A/G]GAAGGCTGAAGACAC | 9169 |
rs754027694 | snp | C/T | 6.62021e-05 | 0.00575297 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927802 | AACATGCCCAAGCAA[C/T]TGAACCTCTGGGCTC | 9169 |
rs754110337 | snp | A/G | 4.37857e-05 | 0.00467878 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964220 | AATAGAGAATTTTAT[A/G]TTTGCCTTCTCCCAA | 9169 |
rs754112741 | snp | A/G | 1.65315e-05 | 0.00287498 | missense | SCAF11 | GRCh38.p7 | 12:45926607 | TGGTTCTTGGATCAG[A/G]CCCAGAGTTTATTTT | 9169 |
rs754125866 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921646 | AAAAATCATAAAGAT[C/T]ATACTTTACATTTTA | 9169 |
rs754170486 | snp | C/T | 1.68207e-05 | 0.00290001 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934495 | TCCTGTTTCACTGTA[C/T]AAAGAGTTTCCTGTA | 9169 |
rs754194301 | snp | C/G | 0.000163572 | 0.00904209 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991913 | GCTTTCAGCCGCGCG[C/G]TCACACGTTTTCCTG | 9169 |
rs754262807 | snp | C/T | 1.64825e-05 | 0.00287071 | missense | SCAF11 | GRCh38.p7 | 12:45928331 | GCAGTATGCTTCTCA[C/T]TTTCTTCTATTTGCT | 9169 |
rs754285378 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930456 | TTTGTTTTTTTTTTG[-/T]TTTTTTTTTTTTTTT | 9169 |
rs754293684 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971738 | CCCCTTTCTCTGTTC[C/T]TCATGTCCCAATTCC | 9169 |
rs754322684 | snp | C/T | 4.94254e-05 | 0.00497094 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45923095 | TCCTGGGGCTGCTGT[C/T]GGAGCAGGCAAAACT | 9169 |
rs754333857 | snp | A/G | 6.65591e-05 | 0.00576846 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945239 | AATCCACAAGCAAAA[A/G]GTAACTTACTATGTA | 9169 |
rs754334765 | in-del | -/AA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955645 | ACTTACTCTATTTTT[-/AA]GTTATTTTAATTTTG | 9169 |
rs754340536 | in-del | -/GGT | 0.000380395 | 0.013786 | cds-indel | SCAF11 | GRCh38.p7 | 12:45924792 | GATGGTGGGGGAGGG[-/GGT]GGTGGTGGTGGTAGT | 9169 |
rs754350978 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985301 | GATCAACCCCCTGCA[C/T]GTGGCCAGTTTCCCA | 9169 |
rs754400016 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925243 | TTCTAAATAATGTGG[A/T]CTGACTTTCTAATGA | 9169 |
rs754410537 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962843 | CAAATCCTCTGGAGG[A/G]AAGAATACCTAAATT | 9169 |
rs754434374 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | SCAF11 | GRCh38.p7 | 12:45927360 | TTTTGGTTTTATCTA[C/T]GGTATCTTTTGGGCT | 9169 |
rs754467940 | in-del | -/GCA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937157 | TAAAAATAAATTTTT[-/GCA]TTTTTCCTTCCTGAA | 9169 |
rs754513595 | snp | A/C | 1.88578e-05 | 0.00307059 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925086 | GAATCTATCAAAAGA[A/C]AAAAAGCTTGTGAAA | 9169 |
rs754540868 | snp | C/T | 1.71625e-05 | 0.00292933 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926143 | CAAGAATACATTACC[C/T]TGTCCAGATGTTTCC | 9169 |
rs754546203 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963300 | ATGCCTAGAAACAAT[A/G]GAGTAAAACTGTAAA | 9169 |
rs754582306 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946884 | CTCTTGGAGGGGGTA[C/T]TCCATGAATACCTTG | 9169 |
rs754599554 | snp | A/G | 1.67279e-05 | 0.002892 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961715 | CTCTGCCCATTTAAG[A/G]ATACAAGTCATACAG | 9169 |
rs754603513 | snp | A/G | 4.7627e-05 | 0.00487967 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931470 | GAAACTAATAATAAT[A/G]ATTTTTAAAATAGAA | 9169 |
rs754606999 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925674 | CATAAAATTTAACTA[C/G]TAAATTATAAGGTTA | 9169 |
rs754630231 | in-del | -/TCC | 0.000454419 | 0.0150666 | cds-indel | SCAF11 | GRCh38.p7 | 12:45926156 | CCCTGTCCAGATGTT[-/TCC]TCCTCTTGTTTCATC | 9169 |
rs754675632 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987766 | ACTGAGAAGGGAAGC[C/T]ATTTGAGAAAAGAAG | 9169 |
rs754679006 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933258 | AATTTTAGACCTTCA[C/T]CAGAATCTCACAATT | 9169 |
rs754697285 | snp | A/G | 1.89234e-05 | 0.00307593 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931619 | AAACCAATTCTGAAA[A/G]CATAATAAAGACATT | 9169 |
rs754711671 | snp | A/C/G | 0.000115635 | 0.007603 | missense, synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927999 | CAGATAAGTCACTTA[A/C/G]GGGACAAGATACAGG | 9169 |
rs754763295 | snp | C/T | 1.65059e-05 | 0.00287275 | missense | SCAF11 | GRCh38.p7 | 12:45926925 | TTCTGGTTCTCCTTT[C/T]TCTCTCTCTCCTCTG | 9169 |
rs754799829 | snp | C/T | 1.64825e-05 | 0.00287071 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928078 | AAGATGAACTGTACA[C/T]ACATCTGTCTTTACC | 9169 |
rs754816885 | snp | C/G | 0.000890789 | 0.0210856 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922207 | AACCTAAGAAAAAAG[C/G]GGTGGGGGGTAAACT | 9169 |
rs754934647 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953582 | AAAGTGTAATATTTC[C/T]AGTGCTTCCTATTTT | 9169 |
rs754942290 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966527 | AAATTAAAAACAGTG[C/T]GGCTATTAAGGAATA | 9169 |
rs754987729 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952153 | CATTAAATAGGCAGT[C/T]GTGCCAGCAATAAAA | 9169 |
rs755015750 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975032 | TTCTTGGATGGCTAC[A/G]TGCACTGTCAATAAG | 9169 |
rs755024747 | snp | C/T | 3.39368e-05 | 0.00411913 | missense | SCAF11 | GRCh38.p7 | 12:45948441 | TAATCACTAACCTTA[C/T]ACAGCTTTTAGAATT | 9169 |
rs755048902 | snp | A/G | 1.64781e-05 | 0.00287033 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928783 | TCTTGATCCTCTGGT[A/G]TTTGATGTACCAGAA | 9169 |
rs755052918 | snp | C/T | 3.29674e-05 | 0.00405988 | missense | SCAF11 | GRCh38.p7 | 12:45927618 | TTTTAGGCAACTCTG[C/T]AGATCTAGGATGTTC | 9169 |
rs755095036 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930679 | TTTACAGCTGTTTAC[A/T]TTTCTTATGACTGCA | 9169 |
rs755113764 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45944634 | AATAAACAGCCTGAA[C/T]CCCCAAGGAGGAGTC | 9169 |
rs755138616 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980165 | GTAGTAGGACTGGAA[C/T]CCATTAGCAATTTAC | 9169 |
rs755138958 | snp | C/G/T | 3.32205e-05 | 0.00407546 | missense | SCAF11 | GRCh38.p7 | 12:45927708 | TTTTTAGTAAGTTAT[C/G/T]TTCAGAGTCTTGAAT | 9169 |
rs755150221 | snp | C/T | 1.64827e-05 | 0.00287073 | missense | SCAF11 | GRCh38.p7 | 12:45928793 | CTGGTATTTGATGTA[C/T]CAGAAGTTTGCTTCT | 9169 |
rs755164439 | snp | A/G | 5.30293e-05 | 0.00514896 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964235 | GTTTGCCTTCTCCCA[A/G]TAATATCAATTAAAA | 9169 |
rs755165984 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922698 | CTCTCCAACTATTAA[C/T]GTGACAAATATAAAA | 9169 |
rs755203713 | snp | C/T | 1.65233e-05 | 0.00287426 | missense | SCAF11 | GRCh38.p7 | 12:45926619 | CAGGCCCAGAGTTTA[C/T]TTTTTCTGTTATCCA | 9169 |
rs755216334 | snp | C/T | 1.96907e-05 | 0.00313767 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934280 | ACTCCAATTTGATCT[C/T]TGAGGCTAGAAAAGT | 9169 |
rs755237607 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942835 | AAAGCATTTATTACC[G/T]CCTGTTTTATATTTA | 9169 |
rs755238034 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992423 | CAAAATCAGAGCAAA[C/T]AGTAAAGGATATATA | 9169 |
rs755264249 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977942 | ATCAGTTCCAAAACC[C/T]TAATGATAGCATGGG | 9169 |
rs755267265 | snp | G/T | 0.000280013 | 0.0118291 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922973 | GCGCTGGCTTCCACT[G/T]CAACACTTACTTTGC | 9169 |
rs755307214 | snp | A/C | 3.38158e-05 | 0.00411178 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934514 | GAGTTTCCTGTACAA[A/C]GACATAAAAGGACTT | 9169 |
rs755364217 | snp | C/T | 1.64787e-05 | 0.00287038 | missense | SCAF11 | GRCh38.p7 | 12:45926699 | TCTAGATGGATGTCA[C/T]TTTTTTCTTTTCTTG | 9169 |
rs755387622 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920704 | CACAGGTTTTACTGT[C/T]TAGAATTTTGCAACA | 9169 |
rs755395187 | snp | C/T | 3.29647e-05 | 0.00405971 | missense | SCAF11 | GRCh38.p7 | 12:45928335 | TATGCTTCTCACTTT[C/T]TTCTATTTGCTCATT | 9169 |
rs755436048 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958721 | GCTATGGGCCATGAA[A/G]GCTACCACAGGTTCA | 9169 |
rs755457299 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936140 | TACTCTATGTGTGGT[C/T]TTTTTTGTTTTTTTT | 9169 |
rs755479979 | snp | C/T | 1.64817e-05 | 0.00287064 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928426 | ACTACTGTCTACATC[C/T]GGTTGGTGCTCTTTT | 9169 |
rs755480010 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952970 | TTGTGTATGGTCCTT[A/G]ATCATTTAACACATT | 9169 |
rs755517989 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971757 | TGTCCCAATTCCCAA[A/C]TGATCTGGTGATGGT | 9169 |
rs755575410 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985303 | TCAACCCCCTGCATG[C/T]GGCCAGTTTCCCATT | 9169 |
rs755588126 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959962 | AATAGCAGCATAAAG[A/G]TAAGTACTTTCTTTT | 9169 |
rs755602543 | in-del | -/TCT | 0.000935891 | 0.0216118 | cds-indel | SCAF11 | GRCh38.p7 | 12:45926162 | CCAGATGTTTCCTCC[-/TCT]TGTTTCATCCATCCA | 9169 |
rs755627699 | snp | C/T | 1.64846e-05 | 0.0028709 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928315 | CTCTGTATCATAATT[C/T]GCAGTATGCTTCTCA | 9169 |
rs755632813 | in-del | -/T | 1.64827e-05 | 0.00287073 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45928503 | ATCATTGGAAGATGA[-/T]TTTTTCAGGGGCAGC | 9169 |
rs755702886 | snp | C/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990920 | TGGTGCGCATGCGCA[C/G]CGCGTGGACTTTGGC | 9169 |
rs755737164 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938184 | TTTGTGGCTTAAACT[C/T]TGTGGCTTAAAACTC | 9169 |
rs755740479 | snp | A/G | 1.66026e-05 | 0.00288115 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45951719 | GTCAATAGGACATGA[A/G]GCCAGTGTCTGAAAA | 9169 |
rs755801547 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986854 | CACTATGTAAGAAGT[A/G]CCCTTCTCCTCCCAC | 9169 |
rs755822272 | snp | G/T | 0.000728951 | 0.0190773 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956199 | ATAGCTCCTCTTAGA[G/T]AGAGAGAAACAAGTG | 9169 |
rs755830348 | snp | C/T | 1.64871e-05 | 0.00287111 | missense | SCAF11 | GRCh38.p7 | 12:45928802 | GATGTACCAGAAGTT[C/T]GCTTCTTTTCTTCCC | 9169 |
rs755840808 | snp | A/C | 7.21163e-05 | 0.00600441 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928904 | AAAAAATATGTTTTA[A/C]GAAATAGTAATTTGG | 9169 |
rs755852089 | snp | A/G | 1.69807e-05 | 0.00291377 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45925067 | TGTTTGGTCTTTTAG[A/G]CTAGAATCTATCAAA | 9169 |
rs755858107 | snp | C/T | 0.000104371 | 0.00722321 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926136 | AAACCAACAAGAATA[C/T]ATTACCCTGTCCAGA | 9169 |
rs755886557 | snp | C/T | 8.28686e-05 | 0.00643641 | missense | SCAF11 | GRCh38.p7 | 12:45927854 | GTCTGTATAATTTCA[C/T]CCTCAGAAGATTCTA | 9169 |
rs755912651 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934763 | TGCTATGTTTACAAC[-/AT]ATGAGTTAAAATTCT | 9169 |
rs755927101 | snp | C/T | 1.78519e-05 | 0.00298758 | missense | SCAF11 | GRCh38.p7 | 12:45931607 | TTCCAGGGTATAAAA[C/T]CAATTCTGAAAACAT | 9169 |
rs756050415 | snp | C/T | 3.29516e-05 | 0.00405891 | missense | SCAF11 | GRCh38.p7 | 12:45926765 | TACCGATCATTTCCT[C/T]GTGGACATCTCCAAC | 9169 |
rs756101310 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966324 | CAAGCAAAGGCCCAG[C/T]GATCTTTTGTGGGAT | 9169 |
rs756111989 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979594 | CCCTTACAAATTGGT[A/G]CAAGTAGTTATTATA | 9169 |
rs756138488 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967234 | TTAAAAAAAAAACAA[C/T]CTACAATTAATATTT | 9169 |
rs756152988 | snp | C/G | 1.64808e-05 | 0.00287057 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928579 | TCTTCTTACAGACTT[C/G]CGTTTTGGAGCCTGT | 9169 |
rs756156338 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965130 | CTGAGAACCTTAGAT[G/T]CAATCTTACAAATTC | 9169 |
rs756207657 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977501 | TGACTGTAGTGGTAA[C/T]ACAGATCTATACATG | 9169 |
rs756243794 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942549 | TACTCTTTCTCCTCC[A/G]TCTACCTAATTCAGT | 9169 |
rs756244682 | snp | C/T | 1.64795e-05 | 0.00287045 | missense | SCAF11 | GRCh38.p7 | 12:45927462 | AGTGTGTCACAGAAT[C/T]TTCATTCATTTGTTT | 9169 |
rs756296846 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941650 | TCTCCCACCAGCCTT[C/T]CCCATTTCAGTAACT | 9169 |
rs756316511 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975319 | CTTTGAAGCCAGGCA[C/T]TGACTTCTCCTCTCT | 9169 |
rs756335469 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980269 | CTTAATGATTCAAAT[A/G]ACTGCAAAAATGTTA | 9169 |
rs756379531 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957848 | CTTATTTTAAGGGCC[A/G]AATTTTTAATCACTT | 9169 |
rs756407105 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956355 | TCAAAATCAAATAAA[A/G]ATGACTTAGAAATGC | 9169 |
rs756458605 | snp | C/T | 1.65168e-05 | 0.00287369 | missense | SCAF11 | GRCh38.p7 | 12:45926484 | GGTTGCCTCTGCCTC[C/T]ACCACGGTTAGATAC | 9169 |
rs756485836 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924588 | GGATAGTGAAAGAGG[G/T]ATTATGAAGGTTTAC | 9169 |
rs756501243 | snp | A/G | 1.67492e-05 | 0.00289384 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45922579 | TTTCTTGAATTTGCA[A/G]TTTCTGATGAGAAGA | 9169 |
rs756537439 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934575 | GCTGTAAACCAGCAT[C/T]GATACCAGCACATTG | 9169 |
rs756554611 | snp | A/G | 3.29538e-05 | 0.00405904 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922949 | GCCTTGTCTGTCTTC[A/G]AGCTATCTGCGCTGG | 9169 |
rs756587911 | snp | G/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919481 | TAACGGGACCAAGGT[G/T]TCAAAGATCAATACT | 9169 |
rs756592710 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948001 | AAATTTTACATTGCT[C/G]AACATTTTATTTTAC | 9169 |
rs756624718 | snp | A/G | 1.84824e-05 | 0.00303988 | missense | SCAF11 | GRCh38.p7 | 12:45934236 | GAAGAAAACATATTG[A/G]AGAAAAAATTTCTGA | 9169 |
rs756642767 | in-del | -/TGA | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991220 | GAGAGCTTTCCCGCC[-/TGA]TGACTCCCCGAGCCT | 9169 |
rs756647624 | snp | C/T | 1.68366e-05 | 0.00290138 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934471 | CTTTATTGCTGCATT[C/T]TTCTTTCCTCCTGTT | 9169 |
rs756653103 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955959 | TCTGTACTAAGGTTG[C/T]TGTATCAGTTAAGAA | 9169 |
rs756659852 | snp | A/G | 1.64817e-05 | 0.00287064 | missense | SCAF11 | GRCh38.p7 | 12:45928104 | TTACCTCTGATTGTG[A/G]AAGTCCAGATATCTG | 9169 |
rs756679705 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983964 | GGGTTTAAAGATTGA[C/G]AACACTTTTAATTTT | 9169 |
rs756723836 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982653 | AAGGTTACAGTGAAC[C/T]GAGATTGTACCACTG | 9169 |
rs756734333 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972046 | TTTTTGAACTCCTAA[C/T]TCACCCAAGCTGAAC | 9169 |
rs756737040 | in-del | -/ATT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958592 | TTCTATATAATCATC[-/ATT]ATTTTATAAATCAAC | 9169 |
rs756737509 | in-del | -/AC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951180 | TTGTTTTTCAGGAAA[-/AC]ACAGTTTTCAGTTAT | 9169 |
rs756741519 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972585 | AAAACCCTGTCTCTT[-/A]AAAAAAAAAAAAAAA | 9169 |
rs756755219 | snp | C/T | 1.64906e-05 | 0.00287142 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928246 | CCCTTCCTCACCAAC[C/T]AGCACAGGAAGATCT | 9169 |
rs756767518 | snp | C/T | 1.86893e-05 | 0.00305685 | missense | SCAF11 | GRCh38.p7 | 12:45934215 | GATTCTCCAGAGTGG[C/T]TAACAGAAGAAAACA | 9169 |
rs756819768 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937832 | AGTTTAAATCTGGTT[C/G]AAATACTCATTTTAG | 9169 |
rs756820157 | snp | G/T | 1.64909e-05 | 0.00287144 | missense | SCAF11 | GRCh38.p7 | 12:45928223 | GTATTCTCGAGTTTT[G/T]TAACTTCCCCTTCCT | 9169 |
rs756823958 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920890 | AGGATAACAGCCTAA[C/T]AGCAATTCTCGAATT | 9169 |
rs756831657 | snp | A/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991099 | GTGGATTGAGTGTTC[A/T]CCTGGCTGCGCTGCC | 9169 |
rs756869938 | in-del | -/C | 1.67708e-05 | 0.00289571 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945355 | GAATTAAGAAAAAAA[-/C]TGTCATTTTGCTCAC | 9169 |
rs756922160 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985396 | TCCTGGGATGCACCC[C/T]TTACCCCATACTTCT | 9169 |
rs756931787 | snp | A/T | 1.65897e-05 | 0.00288003 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45951701 | TGCCTGAAAAGGTTT[A/T]CGGTCAATAGGACAT | 9169 |
rs756935736 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965012 | GGGGTTGGCATGTAA[A/G]CCATGAATTTTATCT | 9169 |
rs756989778 | snp | C/T | 6.66789e-05 | 0.00577365 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951632 | ATATAATTCATGTTG[C/T]AGAATAAAAAGACTT | 9169 |
rs756992872 | snp | A/G | 4.95127e-05 | 0.00497533 | missense | SCAF11 | GRCh38.p7 | 12:45927249 | TTTCTCTTCTGGGAG[A/G]TGGAGACTGGGGCCG | 9169 |
rs757018168 | snp | C/T | 6.59044e-05 | 0.00574002 | missense | SCAF11 | GRCh38.p7 | 12:45924958 | ATGGGAAGATATTCA[C/T]AGGCTGGTGTTGTGC | 9169 |
rs757050386 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959254 | CCTGGGTGACAGACT[-/T]GAGACTCTGTCTCAA | 9169 |
rs757071059 | snp | C/T | 5.0229e-05 | 0.00501118 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45925061 | CTGGTTTGTTTGGTC[C/T]TTTAGGCTAGAATCT | 9169 |
rs757158216 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925981 | TGTAGATAAACGTAC[A/G]TGTATATATATTTAT | 9169 |
rs757180349 | snp | A/G | 1.65037e-05 | 0.00287256 | missense | SCAF11 | GRCh38.p7 | 12:45927261 | GAGATGGAGACTGGG[A/G]CCGCTTCTTTTCTTG | 9169 |
rs757207107 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963721 | TACATTGAGATTAGG[A/G]TGATCAGAGTTAAAG | 9169 |
rs757233340 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941616 | AAAAGAGAATTCTTC[A/C]TTATACCCTCCCAAA | 9169 |
rs757249326 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977291 | ATGAACTAGCATTTC[A/G]TTCAACAAATTGTAT | 9169 |
rs757286275 | in-del | -/T | 0.000745838 | 0.0192967 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928868 | AAGTACCTAATAATA[-/T]TTTAAAAAAAAAAAA | 9169 |
rs757296499 | snp | C/T | 9.95735e-05 | 0.00705527 | missense | SCAF11 | GRCh38.p7 | 12:45927728 | GAGTCTTGAATATTA[C/T]TGAAATCTTCATTCC | 9169 |
rs757298459 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990786 | ACTGCTGTTTGAGAC[C/T]GAGAAGCGTGGTGGG | 9169 |
rs757305635 | snp | A/C | 3.49016e-05 | 0.00417727 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948413 | CCACTCATTTGCATT[A/C]CACTTCTAAAGTTAA | 9169 |
rs757348461 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940929 | CCCACCTCAGCCTCC[C/T]GAGTAGCTGGGACTA | 9169 |
rs757349659 | snp | A/G | 1.64838e-05 | 0.00287083 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928459 | TAACACAGGTGATGT[A/G]TCAGATTCTGCTGTT | 9169 |
rs757363156 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989385 | TGCTTAAGTATCTTA[C/G]GTCAGTGGTAGCATG | 9169 |
rs757387642 | snp | A/C | 1.64887e-05 | 0.00287125 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923116 | AGGCAAAACTGGTGT[A/C]CTCATGTTATTACTT | 9169 |
rs757399434 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957528 | GTTTAGGAGAGAAAC[A/C]ATGCCTTTGCCAACT | 9169 |
rs757440988 | snp | G/T | 1.85582e-05 | 0.00304611 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924685 | GAACAGCTAAATGTT[G/T]ACAATGGCTATATTG | 9169 |
rs757459758 | snp | A/T | 1.64814e-05 | 0.00287061 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928570 | TTTTCTTCCTCTTCT[A/T]ACAGACTTCCGTTTT | 9169 |
rs757494322 | snp | C/G | 3.30907e-05 | 0.00406746 | missense | SCAF11 | GRCh38.p7 | 12:45924783 | ACTTGTTGGGATGGT[C/G]GGGGAGGGGGTGGTG | 9169 |
rs757503714 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969044 | AAGTGTGGACAGTGC[A/C]TGTGAGAAACTAAAT | 9169 |
rs757561730 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968124 | GCTTTATAATCATGT[A/T]ATATTCTACCTATAC | 9169 |
rs757581696 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982550 | TTTCTACTAAAAATA[C/T]AAAAATTAGCCGGGT | 9169 |
rs757594531 | in-del | -/TTA | 1.66288e-05 | 0.00288343 | cds-indel | SCAF11 | GRCh38.p7 | 12:45925056 | CTTGCTGGTTTGTTT[-/TTA]GGTCTTTTAGGCTAG | 9169 |
rs757602313 | snp | A/G | 4.9436e-05 | 0.00497148 | missense | SCAF11 | GRCh38.p7 | 12:45927452 | TTTTCAGAACAGTGT[A/G]TCACAGAATTTTCAT | 9169 |
rs757635006 | in-del | -/GTA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981130 | GATTATCACCTAAAT[-/GTA]GTAATCTTATTATAA | 9169 |
rs757657401 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989443 | GAACAACAGTCAGCT[-/G]GTAGACACTGTATGT | 9169 |
rs757699585 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981470 | CTTACAGCTCTGAGA[G/T]TCCTGTCTCCCAAAA | 9169 |
rs757730071 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961558 | AGAAAATGACTGACA[A/G]AATTTGAATAATACA | 9169 |
rs757777284 | snp | C/T | 2.0864e-05 | 0.00322979 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931637 | TAATAAAGACATTTT[C/T]GTTTAAATGGTTTAA | 9169 |
rs757797205 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925256 | GGACTGACTTTCTAA[C/T]GAAAGAAAACATTTG | 9169 |
rs757809416 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946686 | TCACAGCCAGTGATA[G/T]GAGTTGTATCAAGAA | 9169 |
rs757813247 | snp | C/T | 3.30202e-05 | 0.00406313 | missense | SCAF11 | GRCh38.p7 | 12:45926465 | CTGTAAGTGCCTCTG[C/T]CACGGTTGCCTCTGC | 9169 |
rs757815461 | snp | C/G | 1.74275e-05 | 0.00295186 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961899 | CTTTCAAGTTCTCCA[C/G]ACCAAAAATCTTGTG | 9169 |
rs757837088 | snp | C/T | 1.90304e-05 | 0.00308461 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922230 | GGTAAACTTTTTTCA[C/T]GCTTAAAGGGATTAA | 9169 |
rs757840404 | snp | A/G | 1.64757e-05 | 0.00287012 | stop-gained | SCAF11 | GRCh38.p7 | 12:45926328 | CCTGTTCACTTTTTC[A/G]CTTATAGGATTGCTG | 9169 |
rs757867125 | snp | C/T | 1.6516e-05 | 0.00287362 | missense | SCAF11 | GRCh38.p7 | 12:45928004 | AAGTCACTTAGGGGA[C/T]AAGATACAGGTTGGT | 9169 |
rs757911670 | snp | C/T | 1.73854e-05 | 0.00294829 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961894 | ATGTGCTTTCAAGTT[C/T]TCCAGACCAAAAATC | 9169 |
rs757945577 | snp | G/T | 1.67531e-05 | 0.00289418 | missense | SCAF11 | GRCh38.p7 | 12:45933143 | TACCTTCCAATTCCA[G/T]GTAATGTATCAGGAA | 9169 |
rs757980161 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934607 | CAAGGGTTGAAATAC[A/G]TAGAAAAGCTGTATT | 9169 |
rs758007686 | snp | A/G | 1.83538e-05 | 0.00302929 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922220 | AGGGGTGGGGGGTAA[A/G]CTTTTTTCATGCTTA | 9169 |
rs758061040 | snp | A/G | 1.64999e-05 | 0.00287222 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45922508 | ATATTCTTCCTTGGT[A/G]ATATCTTTATTTTGG | 9169 |
rs758061399 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975988 | AGTAAACACAAGTTG[C/T]TGGAAAAACGGTGGC | 9169 |
rs758108786 | snp | A/C | 1.64833e-05 | 0.00287078 | missense | SCAF11 | GRCh38.p7 | 12:45928087 | TGTACATACATCTGT[A/C]TTTACCTCTGATTGT | 9169 |
rs758117315 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963434 | AGGGAAAAAAAATGA[A/G]TAATATCTTCAAAGT | 9169 |
rs758121681 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962048 | CTTAAATTTTTTTAA[C/T]GGGGGACTGAAACAA | 9169 |
rs758155797 | in-del | -/T | 1.65696e-05 | 0.00287828 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45948523 | TGTTTCTCTCAGCTG[-/T]TTTTTTACTTGAACC | 9169 |
rs758174696 | snp | A/C/G | 0.000329844 | 0.0128387 | missense, synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927060 | CTCTTCTTGGGGACA[A/C/G]TGATTCAGATCTTCT | 9169 |
rs758249545 | snp | C/G | 3.3644e-05 | 0.00410132 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951602 | ATCAAAGTCAAACAG[C/G]TTCAATTAATTTTTA | 9169 |
rs758257504 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989330 | AAATTTAACATCAGC[A/G]TCTACTACACAAAGC | 9169 |
rs758327687 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940684 | ACTTGGCTTCCCATC[C/T]TTTTGGAATACTTCA | 9169 |
rs758340116 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975420 | TTAGTATAGCCACTT[C/T]CATCAATGATGTTAG | 9169 |
rs758385258 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955734 | TTACCATTTTGATTC[C/T]TTATATACAACAAAA | 9169 |
rs758406448 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968839 | GCTGAGGCAGGAGAA[C/T]TGCTTGAACCCAGGA | 9169 |
rs758420974 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939629 | TTTGAACCCAGGAGG[C/T]GGAGGTTGCAGTGAG | 9169 |
rs758424248 | snp | C/T | 1.65877e-05 | 0.00287986 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45951683 | TGCACTGAATTTAAA[C/T]ACTGCCTGAAAAGGT | 9169 |
rs758461853 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943712 | TCATAATTACCTCAG[C/T]ATCAGCACTCTTGTA | 9169 |
rs758469009 | snp | C/G | 0.000162351 | 0.00900828 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991985 | CCACCCTGACGCCTG[C/G]CCGGGATGAGTTTCC | 9169 |
rs758469528 | snp | A/C | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921748 | CTCCATTGCCCTAAT[A/C]AAAAAGCTATACATT | 9169 |
rs758478592 | snp | A/G | 1.64757e-05 | 0.00287012 | missense | SCAF11 | GRCh38.p7 | 12:45928715 | TGACTGGCTGTTTCA[A/G]CTCTTGTGTTACGTG | 9169 |
rs758525992 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967727 | CCTTAACATGTCCTC[C/T]ATTAACTGTTTTTAT | 9169 |
rs758535790 | snp | C/T | 1.65187e-05 | 0.00287386 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926626 | AGAGTTTATTTTTTC[C/T]GTTATCCAATTGGGA | 9169 |
rs758553998 | snp | C/T | 1.64765e-05 | 0.00287019 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926725 | TCTTGTATTTTCATT[C/T]TGTTTCTCTGGGTCA | 9169 |
rs758579190 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952197 | ATGAAGAAAATGAAG[A/T]ACTCCTTCACCCCTC | 9169 |
rs758593226 | snp | A/C | 8.48529e-05 | 0.00651301 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934526 | CAAAGACATAAAAGG[A/C]CTTGGTTACCTTGTA | 9169 |
rs758650702 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981281 | ACATGTTAATGAGAA[A/C]GGAAACAGGGATGAA | 9169 |
rs758670891 | snp | C/T | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45919026 | TACGTAACCATGATG[C/T]GAATGACTGGTACAA | 9169 |
rs758683422 | snp | A/T | 1.66136e-05 | 0.00288211 | missense | SCAF11 | GRCh38.p7 | 12:45945258 | ACTTACTATGTATCC[A/T]CTTCAAGTCACAAAC | 9169 |
rs758790487 | snp | A/G | 1.70563e-05 | 0.00292025 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923201 | TTACTTGTACTCGAT[A/G]GAAGTCTTTTAGTGA | 9169 |
rs758793682 | snp | C/G | 1.64808e-05 | 0.00287057 | missense | SCAF11 | GRCh38.p7 | 12:45928553 | TTTTTCAGTAAAGGT[C/G]GTTTTCTTCCTCTTC | 9169 |
rs758794586 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987085 | GACCCCTTAGGCTGG[A/G]TGTGGTGGTTCATTC | 9169 |
rs758809961 | in-del | -/CTACTCTTTCCTCTGTATCAT | 1.64838e-05 | 0.00287083 | cds-indel | SCAF11 | GRCh38.p7 | 12:45928289 | CAGAAGATGAAGATC[-/CTACTCTTTCCTCTGTATCAT]CTACTCTTTCCTCTG | 9169 |
rs758860707 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973782 | GAATGTGAAACAAAA[G/T]GTATTCAAAGTGGAA | 9169 |
rs758874722 | snp | A/C | 3.29592e-05 | 0.00405938 | missense | SCAF11 | GRCh38.p7 | 12:45927444 | GCATATTATTTTCAG[A/C]ACAGTGTGTCACAGA | 9169 |
rs758902155 | snp | G/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993199 | TGTCAACATTTTAGA[G/T]TTGATTTTAACTGTA | 9169 |
rs758903182 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45944853 | CTTCCTTCAGGAACT[A/G]TGAATTACTTTCTTG | 9169 |
rs758918255 | snp | C/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921817 | GCACATTCCTTTAAA[C/G]CCTTTACTTTCCCTT | 9169 |
rs758970344 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | SCAF11 | GRCh38.p7 | 12:45928650 | AAGATGGATTACTGT[C/T]ACCTGGGGCATCACA | 9169 |
rs758992214 | snp | G/T | 5.00764e-05 | 0.00500357 | missense | SCAF11 | GRCh38.p7 | 12:45926164 | AGATGTTTCCTCCTC[G/T]TGTTTCATCCATCCA | 9169 |
rs759007617 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958753 | CCTGAAACATTTTGC[C/T]CTAAGTAAAGAGGAT | 9169 |
rs759047049 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973143 | ACAACCAAATGGAAA[C/T]CAACAAAAAGTGAAA | 9169 |
rs759060509 | snp | C/T | 1.64795e-05 | 0.00287045 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927532 | TTGGTCACTGCAAAA[C/T]GAATCACACTCCATA | 9169 |
rs759076242 | snp | A/G | 1.67052e-05 | 0.00289004 | missense | SCAF11 | GRCh38.p7 | 12:45924753 | TTTCCATCTGGTTGT[A/G]AAGCAATGTAGTTGA | 9169 |
rs759086215 | snp | C/G | | | missense | SCAF11 | GRCh38.p7 | 12:45928137 | CTTGCTTTTCCAATG[C/G]ATCACCTCCTTTTTC | 9169 |
rs759088643 | snp | C/T | 1.64811e-05 | 0.00287059 | missense | SCAF11 | GRCh38.p7 | 12:45927432 | GATCAGAAGACGGCA[C/T]ATTATTTTCAGAACA | 9169 |
rs759213054 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941356 | CGTACACATTGTGAA[A/T]ATAATCACCACAAAC | 9169 |
rs759215158 | snp | C/G | 1.64743e-05 | 0.00287 | missense | SCAF11 | GRCh38.p7 | 12:45926308 | TGGTGTATCAAATGA[C/G]AACTCCTGTTCACTT | 9169 |
rs759239345 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969227 | TCCATTTTAACAGTT[C/G]CTGGGTACCTCAAGC | 9169 |
rs759322011 | snp | C/T | 0.00013155 | 0.00810912 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964134 | CATACTTCTTATCTC[C/T]CATATTTAGGGTACA | 9169 |
rs759372295 | snp | A/G | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918737 | AAGAGAATATTATAC[A/G]GCCAGTATAAATCAT | 9169 |
rs759372496 | snp | C/T | 4.95143e-05 | 0.00497541 | missense | SCAF11 | GRCh38.p7 | 12:45926430 | GATTTTCATTCTGAT[C/T]TTTATAGGCAAAACT | 9169 |
rs759403767 | snp | G/T | 2.18443e-05 | 0.0033048 | missense | SCAF11 | GRCh38.p7 | 12:45934179 | GAAAATACTAACCAA[G/T]AAGCTCTATAGGTAA | 9169 |
rs759432452 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969667 | TAAAGCAAATGCAAG[A/G]ACTAAAAAAAGATAA | 9169 |
rs759454382 | snp | A/C | 1.64789e-05 | 0.0028704 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922453 | ATACTCCACTAAAGC[A/C]ATAACTTACTTTATC | 9169 |
rs759460372 | snp | A/C | 1.65332e-05 | 0.00287512 | missense | SCAF11 | GRCh38.p7 | 12:45926549 | CCTGAATTTTCATTT[A/C]TATTTTCTTCCCAAT | 9169 |
rs759460706 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955532 | GAAAGGTCTCAAAGA[C/T]GTTTTTAGTTTTCAG | 9169 |
rs759473737 | snp | A/G | 0.000172191 | 0.00927717 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953861 | AATAAATAATTCCTA[A/G]AAGAAAGTGTGGCAT | 9169 |
rs759509603 | snp | A/T | 0.000280813 | 0.011846 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922899 | TCTCCTTTATCATAT[A/T]CAGAATTATGAAGGT | 9169 |
rs759517126 | snp | A/C | 1.64898e-05 | 0.00287135 | missense | SCAF11 | GRCh38.p7 | 12:45928205 | ACATTAGCCTCTATA[A/C]CTGTATTCTCGAGTT | 9169 |
rs759578593 | snp | G/T | 1.64773e-05 | 0.00287026 | missense | SCAF11 | GRCh38.p7 | 12:45927318 | TTGTAGATGGAGAAT[G/T]AAATCTAGATCTTCG | 9169 |
rs759588782 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961587 | CAAGGAAATTTGTCC[A/G]AAGTAGGAAGAAAAT | 9169 |
rs759611162 | snp | A/C/T | 4.95432e-05 | 0.0049769 | missense | SCAF11 | GRCh38.p7 | 12:45925038 | GGTAGCTGAGAACCA[A/C/T]CAACTTGCTGGTTTG | 9169 |
rs759614962 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958235 | CTTAACCTGTGTGTG[C/T]TTGTATGTGTTGGAG | 9169 |
rs759666502 | snp | A/G | 3.60985e-05 | 0.00424829 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926093 | TAACATATTAAATTT[A/G]TAATTCTTCAAATAA | 9169 |
rs759667874 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946311 | GTTTGTCTGTGTGTT[-/G]GAAGACCAAGTATCC | 9169 |
rs759689989 | snp | C/T | 3.37872e-05 | 0.00411004 | synonymous-codon, upstream-variant-2KB, missense | SCAF11 | GRCh38.p7 | 12:45961703 | TGTCAGACTTACCTC[C/T]GCCCATTTAAGAATA | 9169 |
rs759716002 | snp | A/T | 0.000103249 | 0.00718427 | missense | SCAF11 | GRCh38.p7 | 12:45928857 | ATCCCTTGCAAGAAG[A/T]ACCTAATAATATTTA | 9169 |
rs759722039 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946097 | TTTTAAAAGGACCAT[C/T]AGGAAATTCTAGCAA | 9169 |
rs759744272 | snp | G/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993944 | ATGGCAATAAAAATG[G/T]GTGAATTCAAAGGAC | 9169 |
rs759746881 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954734 | ATCACCGTGCCTAGC[-/T]TTTTTTTTTTTTTTT | 9169 |
rs759748527 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924146 | ATGCCCGGCCTAGGA[A/T]TCTAAAATTTTTAAA | 9169 |
rs759767121 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947297 | CTCATATTCAATTTA[-/C]CTCAAAAATGTGTTA | 9169 |
rs759786550 | in-del | -/TCCATCT | 1.64803e-05 | 0.00287052 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45927469 | ACAGAATTTTCATTC[-/TCCATCT]ATTTGTTTAAGATCA | 9169 |
rs759829722 | snp | A/T | 3.29495e-05 | 0.00405877 | missense | SCAF11 | GRCh38.p7 | 12:45926850 | TACCAAATGATGAAC[A/T]CTTACTTTTTGTTCT | 9169 |
rs759846733 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45960859 | TAACAATTGGAATGC[A/G]GCTAATGTTAAAATA | 9169 |
rs759863926 | in-del | -/TC | 1.67626e-05 | 0.002895 | splice-acceptor-variant | SCAF11 | GRCh38.p7 | 12:45922582 | CTTGAATTTGCAATT[-/TC]TGATGAGAAGAAAAT | 9169 |
rs759883887 | snp | A/C | 1.68678e-05 | 0.00290407 | missense | SCAF11 | GRCh38.p7 | 12:45931547 | GTTGGAAAAATAGTT[A/C]TTGGCAACACAGAAG | 9169 |
rs759886126 | snp | C/G | 1.65518e-05 | 0.00287674 | missense | SCAF11 | GRCh38.p7 | 12:45927807 | GCCCAAGCAATTGAA[C/G]CTCTGGGCTCTTAAC | 9169 |
rs759946327 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938742 | ATAATAAAGGCTCTG[A/C]GCTTAGAACCCAGTA | 9169 |
rs759965099 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940067 | TTCCAAGTTACACTT[A/C]CAGGTTCTCTTAGTC | 9169 |
rs759997430 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952931 | CGTATCAAGACATGC[C/T]TATACAAGTAAAAGT | 9169 |
rs759998052 | in-del | -/C | 0.000325098 | 0.0127453 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45992002 | CGGGATGAGTTTCCT[-/C]CCCACTTTGCCGCGG | 9169 |
rs760001422 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937721 | ATAATCAAGACTGCC[A/C]GTGCTTTGAAAAATG | 9169 |
rs760045255 | snp | A/C | 3.30224e-05 | 0.00406326 | missense | SCAF11 | GRCh38.p7 | 12:45926982 | TGCTCTGGGACCTGG[A/C]TTTTTCTCCTGGGGA | 9169 |
rs760052711 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951227 | TTGTGGGAGTTGGTC[C/T]TTGAATCTAATACTT | 9169 |
rs760056611 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942298 | TATCATCATCTCCAC[C/T]AATATCTCCTTGGCC | 9169 |
rs760071338 | snp | C/T | 1.76943e-05 | 0.00297436 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948391 | TTTGTACTAGTTAAC[C/T]TCTGTTCCACTCATT | 9169 |
rs760107848 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988904 | AAAACTCACATTGCA[C/T]AAAAAATATAAATTC | 9169 |
rs760138206 | snp | A/G | 1.68408e-05 | 0.00290175 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945360 | AAGAAAAAAACTGTC[A/G]TTTTGCTCACTTATT | 9169 |
rs760152254 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940282 | TAAGTGGGGAGCAGA[C/T]ATTCTGCTATCAAAA | 9169 |
rs760177864 | snp | C/T | 1.66701e-05 | 0.002887 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945227 | AAAAAAAGGTAGAAT[C/T]CACAAGCAAAAAGTA | 9169 |
rs760191387 | snp | A/G | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918632 | GAATTGCTTGAACCC[A/G]GAAGGTGGAGGGTGC | 9169 |
rs760216924 | in-del | -/ATCGTTTCACAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935888 | TGTGGTTTCCTGAAG[-/ATCGTTTCACAA]ATCGTTTCACAAATC | 9169 |
rs760228506 | snp | A/T | 1.68131e-05 | 0.00289935 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923188 | ATCAGTTAATGAATT[A/T]CTTGTACTCGATAGA | 9169 |
rs760297063 | snp | C/T | 1.64803e-05 | 0.00287052 | missense | SCAF11 | GRCh38.p7 | 12:45928409 | TGCACAGTACAAATG[C/T]TACTACTGTCTACAT | 9169 |
rs760360236 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955321 | ACCACCATGCCCAGC[C/T]AATTTTTTGTAGAGA | 9169 |
rs760413759 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953312 | ATTGCTGTTTATCCC[A/G]GTGGCATACCCTGTA | 9169 |
rs760423016 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940955 | GACTACAGGTGTGTA[C/T]CACCACACTTGGCTA | 9169 |
rs760454235 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | SCAF11 | GRCh38.p7 | 12:45927343 | TCTTCGAGTACGAGG[C/G]TTTTTGGTTTTATCT | 9169 |
rs760487893 | snp | A/T | 0.000101942 | 0.00713867 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961862 | GTTTTCTTCACCTGT[A/T]AAAGTAAAACAGCCA | 9169 |
rs760489585 | snp | G/T | 4.94833e-05 | 0.00497385 | missense | SCAF11 | GRCh38.p7 | 12:45926394 | TTGAATTCCCTGAGA[G/T]GGGTTTTCGATTTTG | 9169 |
rs760511994 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980790 | TCTCATGCCCTTTTA[C/G]TGCAAAGAACCTGAG | 9169 |
rs760537221 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985690 | ACAGAGTGGCTGACA[-/C]ATAGTAAATATCTGA | 9169 |
rs760550938 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921117 | CCTCTCGCATAGCTG[A/G]GATTACAGGCGCCCA | 9169 |
rs760553790 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930327 | GTATTGCACTAAACA[C/T]TATGAAAAATATGCA | 9169 |
rs760563452 | snp | C/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993705 | AATCACTTGAACCTG[C/G]GAGGCGGAGGTTGCA | 9169 |
rs760594689 | snp | A/T | 1.65373e-05 | 0.00287548 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922161 | GATTTGCCACTTTAG[A/T]AGAATTTACTTCTCC | 9169 |
rs760610590 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45944100 | CTAGCATAATTTAGT[A/G]GGCCAAATTACCTAG | 9169 |
rs760637160 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957758 | CAAGAACATCCTCAT[C/T]ACATATACTGCAGGT | 9169 |
rs760647438 | snp | C/T | 1.78156e-05 | 0.00298454 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933105 | TTAGCATGTAAACAC[C/T]TGAGTAAATAATTTT | 9169 |
rs760721727 | in-del | -/GGG | 1.65575e-05 | 0.00287724 | cds-indel | SCAF11 | GRCh38.p7 | 12:45924782 | ACTTGTTGGGATGGT[-/GGG]GGGGGAGGGGGTGGT | 9169 |
rs760737715 | snp | C/T | 3.29685e-05 | 0.00405995 | missense | SCAF11 | GRCh38.p7 | 12:45928274 | TCTTGAGCACAAGAC[C/T]CAGAAGATGAAGATC | 9169 |
rs760755774 | snp | A/G | 1.64928e-05 | 0.00287161 | missense | SCAF11 | GRCh38.p7 | 12:45927203 | TCATTCTTAGGAGAT[A/G]GTGATTGAGACTTCC | 9169 |
rs760806419 | in-del | -/TTATT | 1.66055e-05 | 0.0028814 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45927948 | CTAGGGAACTCTCTG[-/TTATT]TTTTCTTCATTAACC | 9169 |
rs760818552 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983722 | GTTCAAAACCAGGTC[-/T]GACTGACTCCTAAAC | 9169 |
rs760825865 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971664 | AGCTGGGGGTAAGGA[A/G]TGTCTCCTTCCTAAT | 9169 |
rs760861928 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959440 | TAAATGAAATTAAAT[A/G]TTAGAATGTGTATGA | 9169 |
rs760863039 | snp | A/G | 1.65957e-05 | 0.00288055 | missense | SCAF11 | GRCh38.p7 | 12:45951666 | TTAACATAACCTTCC[A/G]ATGCACTGAATTTAA | 9169 |
rs760886102 | snp | A/C | 3.2962e-05 | 0.00405954 | missense | SCAF11 | GRCh38.p7 | 12:45925013 | CATTTGCGGTTGCAT[A/C]ATATTTATAGGTAGC | 9169 |
rs760916937 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973657 | ACCGGTGATTTCTTA[C/T]CAGAAACCATGCAAG | 9169 |
rs760938196 | snp | A/T | 1.65209e-05 | 0.00287405 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928831 | CCCTTCTTGAGTATG[A/T]GCTAATGCATATCCC | 9169 |
rs760954536 | snp | C/G | 3.31016e-05 | 0.00406813 | missense | SCAF11 | GRCh38.p7 | 12:45927799 | TTCAACATGCCCAAG[C/G]AATTGAACCTCTGGG | 9169 |
rs761001658 | snp | C/T | 1.64765e-05 | 0.00287019 | missense | SCAF11 | GRCh38.p7 | 12:45928766 | GTCATTGCAGGTTTT[C/T]GTCTTGATCCTCTGG | 9169 |
rs761021254 | snp | A/T | 2.78664e-05 | 0.00373262 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951801 | ATACAATTATAAATT[A/T]TCCATAAAATTATTT | 9169 |
rs761057943 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985216 | TTTGTTCTTGTTTTC[C/T]CCATTACCAAATTTA | 9169 |
rs761063377 | snp | C/T | 0.000176445 | 0.00939102 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991875 | GCTCTGCTCCCCGCG[C/T]GCGGCTCACCCAGGT | 9169 |
rs761087699 | snp | A/G | 3.3216e-05 | 0.00407515 | missense | SCAF11 | GRCh38.p7 | 12:45927701 | AGATTATTTTTTAGT[A/G]AGTTATTTTCAGAGT | 9169 |
rs761122008 | snp | C/T | 1.64846e-05 | 0.0028709 | missense | SCAF11 | GRCh38.p7 | 12:45926682 | AATTTGGATCATCAG[C/T]ATCTAGATGGATGTC | 9169 |
rs761128120 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965748 | CTATATGTATCTGAA[A/T]GGGTTTTTCTATTAA | 9169 |
rs761169912 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986596 | TTCTAAATGACAACA[C/T]TTTTAACAATAAGAT | 9169 |
rs761200083 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949184 | CTCTTATAGATAAAC[C/T]AGATCTTAAAAGAAA | 9169 |
rs761290534 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953198 | CTATTACTTTCCCTA[C/T]AGAAAACTTGACCTT | 9169 |
rs761308021 | snp | A/C | 1.65518e-05 | 0.00287674 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927787 | TACATCTTCAGTTTC[A/C]ACATGCCCAAGCAAT | 9169 |
rs761311811 | snp | A/C | 1.65375e-05 | 0.0028755 | missense | SCAF11 | GRCh38.p7 | 12:45926576 | CAATGAGACTCTTTC[A/C]ACTTTTCTGGATTTC | 9169 |
rs761328140 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | SCAF11 | GRCh38.p7 | 12:45926663 | TTTCTATGTTTGTCA[A/G]CAGAATTTGGATCAT | 9169 |
rs761331395 | in-del | -/AC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922713 | CGTGACAAATATAAA[-/AC]AGTTTATTTACTAAA | 9169 |
rs761343457 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967379 | CAGGTGCCGGTGGCT[C/G]ACGCAAGTAATCCCA | 9169 |
rs761396662 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947008 | ACCCAAAAGTTAACA[A/T]CTAAGGAGCTTACAG | 9169 |
rs761406161 | snp | C/T | 1.64846e-05 | 0.0028709 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922931 | GCTCTCAACCTTGAA[C/T]TTGCCTTGTCTGTCT | 9169 |
rs761438638 | snp | A/G | 1.68621e-05 | 0.00290358 | missense | SCAF11 | GRCh38.p7 | 12:45934466 | TTTATCTTTATTGCT[A/G]CATTTTTCTTTCCTC | 9169 |
rs761463463 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943300 | AAAATATTAAGTGGA[A/G]AATTCCAGATACAAA | 9169 |
rs761497357 | in-del | -/AAT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983061 | AGGCAAGTAAAGAAA[-/AAT]AATGATAATAAAGTG | 9169 |
rs761562226 | snp | C/G | | | missense | SCAF11 | GRCh38.p7 | 12:45928517 | GATTTTTCAGGGGCA[C/G]CTACAGAGCTCCGAA | 9169 |
rs761577075 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980673 | CATATCCTTACAGTA[C/T]TTATGTAACTAATTA | 9169 |
rs761599304 | snp | C/T | 1.66938e-05 | 0.00288905 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945221 | CAACAAAAAAAAAGG[C/T]AGAATCCACAAGCAA | 9169 |
rs761599751 | snp | C/T | 1.6483e-05 | 0.00287076 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928303 | TCCTACTCTTTCCTC[C/T]GTATCATAATTTGCA | 9169 |
rs761630080 | snp | A/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993571 | TAAGGTCAGGAGTTC[A/G]AGACCAGACTGGCCA | 9169 |
rs761636342 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979487 | TAAAACTTTACAGAG[G/T]TTCAATTCCAGAAAT | 9169 |
rs761664000 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930143 | ATCATTTGTTTACAA[A/G]ATGAATCATCTGTCT | 9169 |
rs761675966 | snp | A/C | 1.64757e-05 | 0.00287012 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927334 | AAATCTAGATCTTCG[A/C]GTACGAGGCTTTTTG | 9169 |
rs761705579 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979588 | CTAATCCCTTACAAA[-/T]TTGGTACAAGTAGTT | 9169 |
rs761715226 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943430 | TAAGAAATTTTGAGA[C/G]AGCCCACGCTCACCT | 9169 |
rs761755326 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958329 | CTTTACCTTCCTAAA[C/G]TATGCAAACTCAGAT | 9169 |
rs761787012 | snp | C/T | 1.64795e-05 | 0.00287045 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922437 | TCAAAACAACGTGCA[C/T]ATACTCCACTAAAGC | 9169 |
rs761807282 | snp | C/T | 1.64963e-05 | 0.00287192 | missense | SCAF11 | GRCh38.p7 | 12:45927044 | TTCTCTCTAGAAGTT[C/T]CTCTTCTTGGGGACA | 9169 |
rs761867594 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951925 | GTTGGAATACAATGA[C/T]GAACGAGACAGAATC | 9169 |
rs761877972 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989950 | GGGAGGAGGGTGTCT[G/T]TGGCGGTTCTGGCGT | 9169 |
rs761944483 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949062 | GCATCAGAGAGTAAG[C/T]GGACTTTTTAAAGCA | 9169 |
rs761951774 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971348 | TTCCAGTTCCAGGTA[A/G]GATGGAATAAACACA | 9169 |
rs761958186 | snp | C/T | 1.64849e-05 | 0.00287092 | missense | SCAF11 | GRCh38.p7 | 12:45928163 | TTTTCAAGAATATTT[C/T]CAGAAATCTCACTTT | 9169 |
rs761969125 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983643 | TAAAAAATTAGGTGA[A/G]GAAATTGAGATACTG | 9169 |
rs762003270 | snp | C/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920154 | TATTACAAATGCCCA[C/G]AAATGTAGAATAAAG | 9169 |
rs762022678 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937088 | TATTATTTCTTCATA[C/T]CTGGACACCTGTGCT | 9169 |
rs762028200 | snp | A/T | 1.66073e-05 | 0.00288156 | missense | SCAF11 | GRCh38.p7 | 12:45951657 | AGACTTACCTTAACA[A/T]AACCTTCCAATGCAC | 9169 |
rs762071566 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936103 | TCTAACATTTACTTA[C/T]TACTAAATAACACCC | 9169 |
rs762116331 | snp | A/G | 1.64762e-05 | 0.00287016 | missense | SCAF11 | GRCh38.p7 | 12:45928757 | GTAGGAGTTGTCATT[A/G]CAGGTTTTCGTCTTG | 9169 |
rs762180647 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | SCAF11 | GRCh38.p7 | 12:45928676 | TCACACCCAGAATTG[C/T]CTGATATTGGGGATC | 9169 |
rs762258577 | in-del | -/TAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931460 | GAAACTGGAAGAAAC[-/TAA]TAATAATAATTTTTA | 9169 |
rs762262046 | snp | C/T | 3.29544e-05 | 0.00405908 | missense | SCAF11 | GRCh38.p7 | 12:45924903 | ATGTTAAATGGATTG[C/T]GTTGGATGTTCATCA | 9169 |
rs762273108 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976946 | ACCTCTTGCCAGACT[A/G]ATGATGTAGATAGCC | 9169 |
rs762311972 | in-del | -/G | 1.65127e-05 | 0.00287334 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45928007 | TCACTTAGGGGACAA[-/G]ATACAGGTTGGTACA | 9169 |
rs762316987 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924986 | TGCATTCATTTGTTG[C/T]TGCATTACATTCATT | 9169 |
rs762320316 | in-del | -/CCA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945976 | GATTACAGGCATGAG[-/CCA]CCACGTCTGGCTTCA | 9169 |
rs762321406 | snp | C/T | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926929 | GGTTCTCCTTTCTCT[C/T]TCTCTCCTCTGCCCA | 9169 |
rs762324956 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947813 | TCCTAAGTAGCTGGA[A/G]CTGCAGCCATGTGTC | 9169 |
rs762360867 | snp | C/T | 1.65954e-05 | 0.00288053 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927682 | TTCCAATTTGGTGTT[C/T]AGAAGATTATTTTTT | 9169 |
rs762409367 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975730 | TGTTTGGTCTAATTT[C/T]AATACTGTTGAGAAA | 9169 |
rs762421900 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966126 | GACAAACAACATAAT[A/G]ATGAATGTCCAGGGA | 9169 |
rs762469654 | snp | C/G | 3.30748e-05 | 0.00406649 | missense | SCAF11 | GRCh38.p7 | 12:45926569 | TTCTTCCCAATGAGA[C/G]TCTTTCAACTTTTCT | 9169 |
rs762492110 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979336 | CTAAGAGTTAAAGGG[A/G]GAGAATTAGTGAAAA | 9169 |
rs762493180 | in-del | -/TAATAA | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45919109 | ATTCCCCTGGAACCT[-/TAATAA]TAAAATGTTAAAGAC | 9169 |
rs762534202 | snp | A/G | 4.95184e-05 | 0.00497562 | missense | SCAF11 | GRCh38.p7 | 12:45926438 | TTCTGATCTTTATAG[A/G]CAAAACTACTTCTGT | 9169 |
rs762561112 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964829 | TAGATGTGTTGAGGA[A/G]CTTCAGGCATTCAAG | 9169 |
rs762571952 | snp | A/G | 2.21202e-05 | 0.0033256 | synonymous-codon, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964144 | ATCTCCCATATTTAG[A/G]GTACATACAGTTTTC | 9169 |
rs762642842 | snp | C/T | 1.64914e-05 | 0.00287149 | missense | SCAF11 | GRCh38.p7 | 12:45928215 | CTATACCTGTATTCT[C/T]GAGTTTTTTAACTTC | 9169 |
rs762647591 | snp | C/G | 3.29707e-05 | 0.00406008 | missense | SCAF11 | GRCh38.p7 | 12:45928295 | GATGAAGATCCTACT[C/G]TTTCCTCTGTATCAT | 9169 |
rs762672937 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942421 | TACTCTTATTCGTCT[A/C]TGATTTTCTTCCCTT | 9169 |
rs762689458 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977077 | AAATATTTAAAGGAG[A/T]AATAACACCAAATCA | 9169 |
rs762718597 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941518 | TCCAGAATTTATTCA[C/T]CTTGCATAACTGAAC | 9169 |
rs762725305 | snp | G/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991600 | TTATTTACTTAAAAG[G/T]CCTCCGCGTTGTGGT | 9169 |
rs762732752 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920024 | AAAACAACTAAGGAG[A/G]TGTGCCTTGATATTC | 9169 |
rs762737312 | snp | A/G | 0.00014042 | 0.00837796 | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974259 | CTTTTTGATGGTGGA[A/G]GGTCTTGCTTTGATG | 9169 |
rs762770302 | snp | A/C | | | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990583 | GCTACTCCCCCTTCC[A/C]CCGCCTTGTCTAGCC | 9169 |
rs762806362 | in-del | -/G/GG | 0.00226597 | 0.0335844 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922205 | AAACCTAAGAAAAAA[-/G/GG]GGGGTGGGGGGTAAA | 9169 |
rs762808391 | snp | C/T | 1.64841e-05 | 0.00287085 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928288 | CTCAGAAGATGAAGA[C/T]CCTACTCTTTCCTCT | 9169 |
rs762825866 | snp | C/T | 3.30077e-05 | 0.00406236 | missense | SCAF11 | GRCh38.p7 | 12:45927230 | TTCCTGCTTTCTTTC[C/T]CAGTTTCTCTTCTGG | 9169 |
rs762835769 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983433 | AATGAACTACACATT[C/G]TGGCATGCCTTTCCA | 9169 |
rs762840835 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947428 | TTAAAAAAATGTTTT[A/C]ACATAAACACTTGTT | 9169 |
rs762848274 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971196 | CCTTAACAGAAATTG[C/T]ACTGTTGCATGCAGC | 9169 |
rs762927427 | snp | C/T | 1.70124e-05 | 0.00291649 | missense | SCAF11 | GRCh38.p7 | 12:45931581 | TGAGAGGAAGGACTT[C/T]TGTTTCAACATTCCA | 9169 |
rs762937931 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935291 | CTACTTAATAGCATA[C/T]TAATTTCCTTTTTAG | 9169 |
rs763074104 | snp | C/T | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918902 | GTCTCTTCTTTTACA[C/T]ATTTACTAAAGTTTT | 9169 |
rs763126683 | snp | A/C/G | 3.60252e-05 | 0.004244 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933095 | CTTGTTCATGTTAGC[A/C/G]TGTAAACACCTGAGT | 9169 |
rs763127804 | snp | A/C | 1.65679e-05 | 0.00287814 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927967 | TTTTTCTTCATTAAC[A/C]ACTGACTCTACATTC | 9169 |
rs763145108 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933850 | GGATCAGCTGTAAAA[C/G]GGTTCTTCTTTAGGT | 9169 |
rs763203569 | in-del | -/AAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972586 | AAAACCCTGTCTCTT[-/AAA]AAAAAAAAAAAAAAA | 9169 |
rs763215381 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926863 | ACTCTTACTTTTTGT[C/T]CTACATCTTGAGGGG | 9169 |
rs763228904 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947530 | AACTGATGAAGAATG[C/T]TGTGCTATACTATTA | 9169 |
rs763244633 | snp | C/T | 1.66112e-05 | 0.00288189 | missense | SCAF11 | GRCh38.p7 | 12:45924765 | TGTGAAGCAATGTAG[C/T]TGACTTGTTGGGATG | 9169 |
rs763274719 | in-del | -/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992384 | GATGGAACAACAAAA[-/T]TCTTATGAAGGACCT | 9169 |
rs763284578 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962726 | ACTAAGCCTTAGAAC[C/T]GCTTCAGGAAGGAAA | 9169 |
rs763287001 | snp | A/C | 3.2975e-05 | 0.00406035 | missense | SCAF11 | GRCh38.p7 | 12:45928051 | TGTTAAACATGTAGG[A/C]AAATCATTTGGAAGA | 9169 |
rs763297382 | snp | A/C | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975699 | AGGCAAACTTTCTTC[A/C]TATCAGTGACAAGGC | 9169 |
rs763297870 | in-del | -/TTTC | 2.07308e-05 | 0.00321946 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931635 | ATAATAAAGACATTT[-/TTTC]TTGTTTAAATGGTTT | 9169 |
rs763336674 | snp | C/T | 1.84065e-05 | 0.00303363 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45948529 | TCTCAGCTGTTTTTT[C/T]ACTTGAACCTATGAG | 9169 |
rs763380165 | in-del | -/T | 1.66054e-05 | 0.00288139 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964070 | AAACAACTGTTTTGC[-/T]TTTCAACAAACAAAC | 9169 |
rs763391427 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968381 | TAACATACTTCTATC[A/G]TCCAGTTGCTCTTTT | 9169 |
rs763403184 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939922 | CAATTTGCACAATCC[C/T]CCACTAACTCTACCT | 9169 |
rs763409842 | snp | C/G | 1.6504e-05 | 0.00287258 | missense | SCAF11 | GRCh38.p7 | 12:45927031 | CTGAGATCTTTTGTT[C/G]TCTCTAGAAGTTTCT | 9169 |
rs763441698 | snp | C/T | 1.65072e-05 | 0.00287286 | missense | SCAF11 | GRCh38.p7 | 12:45926447 | TTATAGGCAAAACTA[C/T]TTCTGTAAGTGCCTC | 9169 |
rs763458330 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938978 | AGATTAAAAACAAAA[A/C]TGTATAATTCAGTTA | 9169 |
rs763479426 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961279 | TCTGGTTATTCCACA[A/G]GGCTGATATAAAGAA | 9169 |
rs763483786 | snp | A/G | 9.88631e-05 | 0.00703006 | missense | SCAF11 | GRCh38.p7 | 12:45924882 | TGCAAGGGTAGCTGA[A/G]GATGAATGTTAAATG | 9169 |
rs763496513 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974962 | CACTGGGTTGAAAAA[C/T]GGATGTTGTGTTAGC | 9169 |
rs763529609 | snp | C/T | 1.65138e-05 | 0.00287343 | missense | SCAF11 | GRCh38.p7 | 12:45922521 | GTGATATCTTTATTT[C/T]GGTAAAATGGCTTGA | 9169 |
rs763601227 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949442 | AATAAAATATATCAT[G/T]CAATTTATTTCATTT | 9169 |
rs763614966 | in-del | -/A | 0.072874 | 0.176427 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945209 | AAATTAAAAAACAAC[-/A]AAAAAAAAAGGTAGA | 9169 |
rs763626491 | in-del | -/CGT | 0.000211797 | 0.0102885 | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992099 | CTCCCGCCCTGAGGA[-/CGT]CGTCGCTTTTCTGGC | 9169 |
rs763631095 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985361 | ATAACTTTTTTCTCT[A/C]CTTAGGCTCTGACAT | 9169 |
rs763702119 | in-del | -/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920679 | TAAATTTCCCCTCTG[-/T]TTTCTAAAACACAGG | 9169 |
rs763739113 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942440 | TTTTCTTCCCTTCAC[A/C]GCCAGAGTAATCCTT | 9169 |
rs763816328 | snp | A/C/G | 4.94771e-05 | 0.00497358 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928216 | TATACCTGTATTCTC[A/C/G]AGTTTTTTAACTTCC | 9169 |
rs763834085 | snp | A/G | 1.6486e-05 | 0.00287102 | missense | SCAF11 | GRCh38.p7 | 12:45927153 | TATCCTTTTTTGGGG[A/G]CTGAGAACGGGATTT | 9169 |
rs763843006 | snp | A/C | 1.6489e-05 | 0.00287128 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922922 | ATGAAGGTTGCTCTC[A/C]ACCTTGAACTTGCCT | 9169 |
rs763851728 | snp | C/T | 5.06282e-05 | 0.00503106 | missense | SCAF11 | GRCh38.p7 | 12:45934464 | TATTTATCTTTATTG[C/T]TGCATTTTTCTTTCC | 9169 |
rs763865300 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942638 | TCTCAGGCTTTTACA[C/G]TTGCTGTTCCCTTGC | 9169 |
rs763867140 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979445 | CTGCTTCTGAAATTC[C/T]ACCCCGTTCTGTTTA | 9169 |
rs763911353 | snp | C/T | 3.30087e-05 | 0.00406242 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927241 | TTTCCCAGTTTCTCT[C/T]CTGGGAGATGGAGAC | 9169 |
rs763921340 | snp | C/T | 1.65883e-05 | 0.00287991 | missense | SCAF11 | GRCh38.p7 | 12:45951690 | AATTTAAACACTGCC[C/T]GAAAAGGTTTACGGT | 9169 |
rs763926840 | in-del | -/CATA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950031 | AAACAATCATTCATA[-/CATA]CATACATACATACAT | 9169 |
rs764002668 | snp | C/T | | | upstream-variant-2KB, intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45990732 | GGCCCTGAGTGCATG[C/T]TCGTAGTACCCAGTT | 9169 |
rs764092135 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941525 | TTTATTCATCTTGCA[A/T]AACTGAACCTCTGAA | 9169 |
rs764094424 | snp | A/G/T | 0.000356332 | 0.013344 | intron-variant | SCAF11 | GRCh38.p7 | 12:45953896 | TAAATATTATGTAAG[A/G/T]TCTTGTAATCAACTA | 9169 |
rs764105855 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983949 | TAAATTTACTCAAGA[A/G]GGTTTAAAGATTGAG | 9169 |
rs764120694 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969982 | GCTCACCGCAACCTC[C/T]GCTTCCCAAGTTCAA | 9169 |
rs764123847 | snp | C/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920099 | TTTCTTTACCATAAT[C/G]TAAACGCAAACTTTA | 9169 |
rs764138873 | in-del | -/TTC | 1.65963e-05 | 0.0028806 | cds-indel | SCAF11 | GRCh38.p7 | 12:45927955 | ACTCTCTGTTATTTT[-/TTC]TTCATTAACCACTGA | 9169 |
rs764142120 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957380 | TGTGCAGTCCAGATA[G/T]AAGTCAAGAACTCAC | 9169 |
rs764170062 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983595 | CAGAGACAGAGTTAG[C/G]TGCTATTACCACTGG | 9169 |
rs764187338 | snp | C/T | 1.65586e-05 | 0.00287733 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927970 | TTCTTCATTAACCAC[C/T]GACTCTACATTCTCA | 9169 |
rs764194039 | snp | A/G | 3.29728e-05 | 0.00406021 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928057 | ACATGTAGGAAAATC[A/G]TTTGGAAGATGAACT | 9169 |
rs764194815 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989365 | AAAACATTTTTCAGC[A/G]GTTTTGCTTAAGTAT | 9169 |
rs764210119 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934121 | TTCTAGCAAAAGTTA[A/G]TAATTATTAAACATC | 9169 |
rs764224680 | snp | A/T | 1.75813e-05 | 0.00296485 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948405 | CTTCTGTTCCACTCA[A/T]TTGCATTCCACTTCT | 9169 |
rs764384816 | snp | C/G | 1.6476e-05 | 0.00287014 | missense | SCAF11 | GRCh38.p7 | 12:45926864 | CTCTTACTTTTTGTT[C/G]TACATCTTGAGGGGG | 9169 |
rs764392739 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | SCAF11 | GRCh38.p7 | 12:45928560 | GTAAAGGTGGTTTTC[C/T]TCCTCTTCTTACAGA | 9169 |
rs764452483 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947735 | AGGCTGGAATGCACT[A/G]GTGTGATCATAGCTC | 9169 |
rs764456386 | snp | A/G | 1.71708e-05 | 0.00293003 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923204 | CTTGTACTCGATAGA[A/G]GTCTTTTAGTGATGC | 9169 |
rs764472904 | snp | C/T | 1.65004e-05 | 0.00287227 | missense | SCAF11 | GRCh38.p7 | 12:45927036 | ATCTTTTGTTCTCTC[C/T]AGAAGTTTCTCTTCT | 9169 |
rs764509463 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962766 | GATAGACTCCAGTAT[C/T]AAGCCAAGACTTTTA | 9169 |
rs764509946 | snp | C/T | 4.97327e-05 | 0.00498637 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924773 | AATGTAGTTGACTTG[C/T]TGGGATGGTGGGGGA | 9169 |
rs764549916 | snp | A/G | 1.64803e-05 | 0.00287052 | missense | SCAF11 | GRCh38.p7 | 12:45927447 | TATTATTTTCAGAAC[A/G]GTGTGTCACAGAATT | 9169 |
rs764552227 | snp | C/T | 1.64762e-05 | 0.00287016 | missense | SCAF11 | GRCh38.p7 | 12:45928667 | CCTGGGGCATCACAC[C/T]CAGAATTGTCTGATA | 9169 |
rs764562608 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961307 | GAAGAAATCAAATAA[C/T]CTATGTGAAAAGTCC | 9169 |
rs764612694 | snp | A/T | 1.64798e-05 | 0.00287047 | missense | SCAF11 | GRCh38.p7 | 12:45927433 | ATCAGAAGACGGCAT[A/T]TTATTTTCAGAACAG | 9169 |
rs764640014 | snp | A/G | 1.648e-05 | 0.0028705 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927565 | TATCATTTCATTGTT[A/G]TCCTCACTAAAATGC | 9169 |
rs764655538 | in-del | -/G | 1.65965e-05 | 0.00288062 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45924789 | TGGGATGGTGGGGGA[-/G]GGGGTGGTGGTGGTG | 9169 |
rs764670631 | in-del | -/TA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972848 | AAGATTTAAAGCCAG[-/TA]TATATATATATATAT | 9169 |
rs764679460 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958068 | ACCATGCCTGGCTAA[-/T]TTTTTTTTTTTTTCC | 9169 |
rs764726386 | snp | C/G/T | 3.4833e-05 | 0.00417319 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961897 | TGCTTTCAAGTTCTC[C/G/T]AGACCAAAAATCTTG | 9169 |
rs764798265 | snp | G/T | 2.19142e-05 | 0.00331008 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964139 | TTCTTATCTCCCATA[G/T]TTAGGGTACATACAG | 9169 |
rs764890144 | snp | A/C | 2.13819e-05 | 0.00326963 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934181 | AAATACTAACCAATA[A/C]GCTCTATAGGTAAAG | 9169 |
rs764894430 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957006 | ACAAGTTAAAGTTCT[C/T]GTGGAGCTAGCAATC | 9169 |
rs764912938 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989195 | TGTACTGCCCTGATA[C/T]TCTGCTGCTGAGGTA | 9169 |
rs764924330 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975904 | ACTGATCACATATCA[C/T]AACAGATATAATAAT | 9169 |
rs764933793 | snp | A/C | 0.0596843 | 0.162111 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961871 | ACCTGTTAAAGTAAA[A/C]CAGCCATATGTGCTT | 9169 |
rs764950229 | snp | A/C | 1.728e-05 | 0.00293933 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933115 | AACACCTGAGTAAAT[A/C]ATTTTTTATTTTTAC | 9169 |
rs764959431 | snp | C/T | 1.64749e-05 | 0.00287005 | missense | SCAF11 | GRCh38.p7 | 12:45926319 | ATGAGAACTCCTGTT[C/T]ACTTTTTCGCTTATA | 9169 |
rs764963563 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947009 | CCCAAAAGTTAACAT[A/C]TAAGGAGCTTACAGT | 9169 |
rs764964964 | snp | A/G | 0.000972033 | 0.0220243 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928081 | ATGAACTGTACATAC[A/G]TCTGTCTTTACCTCT | 9169 |
rs765008621 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925698 | AAGGTTATTCAATTT[C/T]TACATCTTCAACAGC | 9169 |
rs765024624 | snp | C/T | 1.79171e-05 | 0.00299303 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922210 | CTAAGAAAAAAGGGG[C/T]GGGGGGTAAACTTTT | 9169 |
rs765047174 | snp | C/T | 1.65064e-05 | 0.00287279 | missense | SCAF11 | GRCh38.p7 | 12:45926435 | TCATTCTGATCTTTA[C/T]AGGCAAAACTACTTC | 9169 |
rs765055697 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978502 | TATTAGTGACAAAAA[A/G]CAAAAGAGCAGTGAG | 9169 |
rs765063695 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940491 | AAGTGGCATTGGATA[C/T]AGAGTCAGAAGACTG | 9169 |
rs765078105 | snp | A/G | 1.64789e-05 | 0.0028704 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922454 | TACTCCACTAAAGCC[A/G]TAACTTACTTTATCT | 9169 |
rs765125623 | snp | C/T | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918788 | GGAAAGTTCTCAGTA[C/T]GTCAAGTGAAAATGA | 9169 |
rs765127322 | snp | C/G | 1.64893e-05 | 0.0028713 | missense | SCAF11 | GRCh38.p7 | 12:45928206 | CATTAGCCTCTATAC[C/G]TGTATTCTCGAGTTT | 9169 |
rs765132929 | in-del | -/CATA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950028 | AGTAAAACAATCATT[-/CATA]CATACATACATACAT | 9169 |
rs765189398 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967597 | TGCAGTGAATCGAGA[G/T]TGCGCCACTGCACTC | 9169 |
rs765217301 | snp | A/T | 1.6489e-05 | 0.00287128 | missense | SCAF11 | GRCh38.p7 | 12:45927140 | CTTTCTCTTGCAATA[A/T]CCTTTTTTGGGGACT | 9169 |
rs765233699 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989973 | TCTGGCGTGGAGCCC[C/T]TTCCCCCCCCCCCGT | 9169 |
rs765238099 | snp | A/G | 3.58854e-05 | 0.00423573 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926107 | TATAATTCTTCAAAT[A/G]AAACAGTATCAATAA | 9169 |
rs765251712 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974946 | AAAATTACTTCTTGA[C/T]CACTGGGTTGAAAAA | 9169 |
rs765255031 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933744 | CTGGCTCAACTAACT[A/G]TACGTGATTTTAAAA | 9169 |
rs765262292 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981994 | AACAAGATATGCCAA[A/G]TAATGCAAACAATAA | 9169 |
rs765315730 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981208 | CAGTCTTCTGCTATG[C/T]TCACCATGACTAACA | 9169 |
rs765355890 | snp | A/G | 1.95777e-05 | 0.00312865 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928862 | TTGCAAGAAGTACCT[A/G]ATAATATTTAAAAAA | 9169 |
rs765432197 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986991 | GCTCTACTCTTAGCT[A/G]AGGCATTCTTAGCTC | 9169 |
rs765433749 | snp | C/T | 1.64768e-05 | 0.00287021 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926707 | GATGTCATTTTTTTC[C/T]TTTCTTGTATTTTCA | 9169 |
rs765524102 | snp | A/G | 1.69536e-05 | 0.00291145 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45931576 | AGAAATGAGAGGAAG[A/G]ACTTCTGTTTCAACA | 9169 |
rs765524257 | snp | A/G | 8.27643e-05 | 0.00643236 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927814 | CAATTGAACCTCTGG[A/G]CTCTTAACAGATTGT | 9169 |
rs765530047 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955924 | TGTATTAAACAGAGC[-/AT]ATGTTTTACTGTGAA | 9169 |
rs765545101 | in-del | -/A | 1.65116e-05 | 0.00287324 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45928010 | CTTAGGGGACAAGAT[-/A]CAGGTTGGTACACTT | 9169 |
rs765547586 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45944635 | ATAAACAGCCTGAAC[C/T]CCCAAGGAGGAGTCA | 9169 |
rs765568231 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | SCAF11 | GRCh38.p7 | 12:45926855 | AATGATGAACTCTTA[C/T]TTTTTGTTCTACATC | 9169 |
rs765607241 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45960910 | TTACTAATTTTTACA[A/G]ACTGACAAATATTAA | 9169 |
rs765635030 | snp | C/T | 1.66236e-05 | 0.00288297 | missense | SCAF11 | GRCh38.p7 | 12:45945251 | AAAAGTAACTTACTA[C/T]GTATCCACTTCAAGT | 9169 |
rs765638595 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966140 | TGATGAATGTCCAGG[C/G]AAGATGACTAAAATG | 9169 |
rs765642450 | in-del | -/AGA | | | cds-indel, intron-variant | SCAF11 | GRCh38.p7 | 12:45920936 | TCGTCTGCAACGGGT[-/AGA]AGAAGATACTATGAA | 9169 |
rs765645876 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959497 | TAGAAGGCTGAAGAC[A/G]CTTATTCCTGATCCT | 9169 |
rs765654930 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921706 | CTCTTTGAAAACCAG[C/T]GCACTTAGAAGTTTC | 9169 |
rs765658053 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974873 | ATCCAAGAAATCACT[A/G]TCTGAAGCAGCTGTA | 9169 |
rs765708719 | in-del | -/TAATAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931460 | GAAACTGGAAGAAAC[-/TAATAA]TAATAATTTTTAAAA | 9169 |
rs765720864 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938759 | CTTAGAACCCAGTAC[A/T]TGGCAGGCATCCAAT | 9169 |
rs765722440 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986410 | AATCCCATCCACTGA[A/G]CCCATCTCCACAATT | 9169 |
rs765726805 | snp | C/T | 1.76618e-05 | 0.00297163 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948399 | AGTTAACTTCTGTTC[C/T]ACTCATTTGCATTCC | 9169 |
rs765761188 | snp | A/G | 1.64822e-05 | 0.00287068 | missense | SCAF11 | GRCh38.p7 | 12:45928421 | ATGTTACTACTGTCT[A/G]CATCTGGTTGGTGCT | 9169 |
rs765766877 | snp | A/G | 3.29636e-05 | 0.00405964 | missense | SCAF11 | GRCh38.p7 | 12:45928427 | CTACTGTCTACATCT[A/G]GTTGGTGCTCTTTTT | 9169 |
rs765775960 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937756 | TAGGTAGAGGACTAG[A/T]AGCCTCATCATTTGA | 9169 |
rs765831196 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975783 | GAGAGATGAGAGAAC[A/C]GCTGGTCAGTGGAGC | 9169 |
rs765846333 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924710 | ATATTGATTAAACTT[C/G]AGTTGCTAAAAACAT | 9169 |
rs765890991 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989014 | CAACAAAAACAAAAG[A/G]CCCATGAACTTTTTC | 9169 |
rs765892734 | snp | A/C | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975121 | AAAATATTCAGTAAA[A/C]CATGCTGTAAACGGA | 9169 |
rs765903062 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987721 | AAATCATAGAGCCTT[-/G]TAGACCATAGGAGTA | 9169 |
rs765987573 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939444 | TTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG | 9169 |
rs766052446 | snp | C/G | 1.65946e-05 | 0.00288046 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961759 | AGCTTTCTGGAAAAC[C/G]AACTTCCTTTTCTAA | 9169 |
rs766098142 | snp | G/T | 3.29527e-05 | 0.00405898 | missense | SCAF11 | GRCh38.p7 | 12:45927356 | GGCTTTTTGGTTTTA[G/T]CTATGGTATCTTTTG | 9169 |
rs766100394 | snp | C/T | 1.68131e-05 | 0.00289935 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922184 | ACTTCTCCACTCTTA[C/T]TATGACAAACCTAAG | 9169 |
rs766165399 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955402 | CGATTGGCCCACCCC[A/G]GCCTCCCAAAGTGTT | 9169 |
rs766193091 | snp | C/T | 1.6473e-05 | 0.00286988 | intron-variant | SCAF11 | GRCh38.p7 | 12:45926138 | ACCAACAAGAATACA[C/T]TACCCTGTCCAGATG | 9169 |
rs766211092 | snp | C/T | 1.64743e-05 | 0.00287 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926296 | AGATCTATCTGCTGG[C/T]GTATCAAATGAGAAC | 9169 |
rs766212242 | snp | C/T | 1.79297e-05 | 0.00299408 | missense | SCAF11 | GRCh38.p7 | 12:45931608 | TCCAGGGTATAAAAC[C/T]AATTCTGAAAACATA | 9169 |
rs766212587 | snp | G/T | 8.51752e-05 | 0.00652536 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961866 | TCTTCACCTGTTAAA[G/T]TAAAACAGCCATATG | 9169 |
rs766278895 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967455 | TCGAGACCAGCCTGG[C/T]CAACATGGCGAAACC | 9169 |
rs766304103 | snp | C/G | 1.77391e-05 | 0.00297813 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933107 | AGCATGTAAACACCT[C/G]AGTAAATAATTTTTT | 9169 |
rs766314011 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983476 | AAAATACCAGAACAC[A/G]ATACATTTAAAAAAT | 9169 |
rs766333673 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979791 | CTCATATGAATATTT[G/T]ACACATAATTTAAAG | 9169 |
rs766377899 | snp | C/T | 3.29902e-05 | 0.00406128 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927208 | CTTAGGAGATGGTGA[C/T]TGAGACTTCCTGCTT | 9169 |
rs766401700 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980807 | GCAAAGAACCTGAGA[A/G]TAGAATAACTGGATT | 9169 |
rs766442993 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924923 | GATGTTCATCAAAGG[A/G]GCATGAACACCCACT | 9169 |
rs766505676 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959462 | TGTGTATGACAGCCT[A/C]GGCATAAGGCATGGC | 9169 |
rs766507492 | in-del | -/AACTT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937250 | ACTTTGAGACTTAAG[-/AACTT]ATCTTCTACTCCTGT | 9169 |
rs766525968 | snp | C/T | 3.32171e-05 | 0.00407522 | missense | SCAF11 | GRCh38.p7 | 12:45927704 | TTATTTTTTAGTAAG[C/T]TATTTTCAGAGTCTT | 9169 |
rs766556988 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973664 | ATTTCTTATCAGAAA[C/T]CATGCAAGTCAGAAG | 9169 |
rs766573353 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957915 | CTCTTTTTTTTGAGA[C/T]AGGGTCTTATTTTGT | 9169 |
rs766619171 | snp | G/T | 1.65908e-05 | 0.00288012 | missense | SCAF11 | GRCh38.p7 | 12:45951673 | AACCTTCCAATGCAC[G/T]GAATTTAAACACTGC | 9169 |
rs766646359 | snp | A/G | | | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922130 | TATTTGTATTTGTCT[A/G]CATAGGCTTTAACCA | 9169 |
rs766659468 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921564 | ACTTTGCAACTGATA[C/T]GTTCTATTTAATATT | 9169 |
rs766667896 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958683 | TTCAATTTGTTCTAG[A/T]GTCCCTAAGGGCAGG | 9169 |
rs766675650 | in-del | -/TAAAAG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946703 | AGTTGTATCAAGAAT[-/TAAAAG]TATTTCTACCAAAAG | 9169 |
rs766696243 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937466 | TTGATCTCTATTATG[C/T]TGATTTTCCTCAAAC | 9169 |
rs766707130 | snp | A/T | 1.64784e-05 | 0.00287035 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928774 | AGGTTTTCGTCTTGA[A/T]CCTCTGGTATTTGAT | 9169 |
rs766708241 | in-del | -/TAGT | 2.10506e-05 | 0.00324421 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934302 | TAGAAAAGTAAAAAG[-/TAGT]TAGTGAAACAGCAAA | 9169 |
rs766722851 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971736 | TCCCCCTTTCTCTGT[C/T]CCTCATGTCCCAATT | 9169 |
rs766724718 | snp | A/G | 4.96537e-05 | 0.00498241 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927801 | CAACATGCCCAAGCA[A/G]TTGAACCTCTGGGCT | 9169 |
rs766768623 | snp | G/T | 0.000164623 | 0.00907106 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991902 | AGGTCCCAGTCGCTT[G/T]CAGCCGCGCGCTCAC | 9169 |
rs766779335 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935792 | AAGCTGTTTCACATA[C/T]TTCTGGGTAATTCTC | 9169 |
rs766795053 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920305 | AAAAGTATTATGCAC[A/G]TAAAATTGAGAAACA | 9169 |
rs766796425 | snp | A/T | | | utr-variant-5-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45990580 | ACCGCTACTCCCCCT[A/T]CCCCCGCCTTGTCTA | 9169 |
rs766802295 | snp | G/T | 1.66551e-05 | 0.00288571 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945233 | AGGTAGAATCCACAA[G/T]CAAAAAGTAACTTAC | 9169 |
rs766867336 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985232 | CCATTACCAAATTTA[C/T]AACTCCCTTCTCACC | 9169 |
rs766886408 | snp | C/G | 6.59381e-05 | 0.00574149 | missense | SCAF11 | GRCh38.p7 | 12:45926685 | TTGGATCATCAGCAT[C/G]TAGATGGATGTCATT | 9169 |
rs766895264 | snp | C/G | 1.64798e-05 | 0.00287047 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922939 | CCTTGAACTTGCCTT[C/G]TCTGTCTTCGAGCTA | 9169 |
rs766896826 | snp | A/G | 3.364e-05 | 0.00410108 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934492 | TCCTCCTGTTTCACT[A/G]TATAAAGAGTTTCCT | 9169 |
rs766958663 | in-del | -/ATAAGAAA | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962567 | ATGCATCGCTGGCTC[-/ATAAGAAA]ATAATAGATACTCTG | 9169 |
rs766996638 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939016 | TGACAGAAGAAAGAA[A/G]GTGATATTTCCTCAA | 9169 |
rs767042584 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940213 | AAGGTTCTAATCTTA[A/C]AGCTATGATTTATGA | 9169 |
rs767066136 | snp | A/G | 9.88321e-05 | 0.00702896 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923058 | TATTACCAGAACTTG[A/G]TCCCTGAACCATTCC | 9169 |
rs767164461 | in-del | -/TT | 3.29658e-05 | 0.00405978 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45928438 | ATCTGGTTGGTGCTC[-/TT]TTTCTAACACAGGTG | 9169 |
rs767181116 | snp | C/T | 4.94279e-05 | 0.00497107 | missense | SCAF11 | GRCh38.p7 | 12:45927338 | CTAGATCTTCGAGTA[C/T]GAGGCTTTTTGGTTT | 9169 |
rs767272602 | snp | A/T | 3.3543e-05 | 0.00409516 | missense | SCAF11 | GRCh38.p7 | 12:45925062 | TGGTTTGTTTGGTCT[A/T]TTAGGCTAGAATCTA | 9169 |
rs767275748 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946072 | ACTAGAGGTAAGCAG[A/T]TATTGTCTTTTTTAA | 9169 |
rs767292485 | snp | A/C | 1.64803e-05 | 0.00287052 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928399 | TACATGAGTCTGCAC[A/C]GTACAAATGTTACTA | 9169 |
rs767331544 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967424 | TGAGGCGGGAGGAGC[A/G]TCTGAGATCAGGAGT | 9169 |
rs767349148 | snp | C/T | 0.000121175 | 0.00778287 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956148 | TTTCTCGCTTCCTCC[C/T]GCTGCTCTATCCTCA | 9169 |
rs767350727 | snp | A/T | 0.0046018 | 0.0477464 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928873 | ACCTAATAATATTTA[A/T]AAAAAAAAAAAAAGT | 9169 |
rs767384686 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966242 | AAGCTTAAGAACATT[A/G]GCAATTATCTTCAAA | 9169 |
rs767435921 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979540 | GAAAGTTACTCTTTC[A/G]TTGGTTTCTTGAGAA | 9169 |
rs767437307 | snp | A/T | 1.66156e-05 | 0.00288228 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961741 | TACAGAAGACATGAT[A/T]ACAGCTTTCTGGAAA | 9169 |
rs767476869 | snp | C/G | 3.29641e-05 | 0.00405968 | missense | SCAF11 | GRCh38.p7 | 12:45928518 | ATTTTTCAGGGGCAG[C/G]TACAGAGCTCCGAAG | 9169 |
rs767502333 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971459 | AAATAATAGCATATG[G/T]ACTAGAGAAGACACC | 9169 |
rs767522688 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979792 | TCATATGAATATTTT[A/G]CACATAATTTAAAGA | 9169 |
rs767559069 | snp | C/T | 1.64749e-05 | 0.00287005 | stop-gained | SCAF11 | GRCh38.p7 | 12:45926275 | GCTGGATGCAGATGT[C/T]CATCCAGATCTATCT | 9169 |
rs767612421 | snp | C/G | 1.64909e-05 | 0.00287144 | missense | SCAF11 | GRCh38.p7 | 12:45927129 | GAGATTGCCTCCTTT[C/G]TCTTGCAATATCCTT | 9169 |
rs767620764 | snp | A/G | 5.81863e-05 | 0.00539349 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948547 | TTGAACCTATGAGAA[A/G]AGCAAAATCAATTTA | 9169 |
rs767631872 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977369 | CAACATATTCTAGAA[C/T]TGCATTTACATGCAA | 9169 |
rs767634132 | in-del | -/AT | 1.65403e-05 | 0.00287574 | frameshift-variant, intron-variant | SCAF11 | GRCh38.p7 | 12:45923149 | TGAGAAGAACTAGGA[-/AT]ATACCCTGTTTTAAA | 9169 |
rs767639017 | snp | A/G | 6.58946e-05 | 0.0057396 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928702 | GGATCTCTGAGACTG[A/G]CTGGCTGTTTCAGCT | 9169 |
rs767766734 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921202 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA | 9169 |
rs767783363 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979722 | ACTCATCCTTCTAGG[C/T]ATCTCAGAGATAAGT | 9169 |
rs767818144 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920209 | TTATGATTACACTCA[C/T]AACAACAAAGCTTAT | 9169 |
rs767825394 | snp | A/G | 1.64784e-05 | 0.00287035 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927577 | GTTGTCCTCACTAAA[A/G]TGCTTCTGAATCTGT | 9169 |
rs767832970 | in-del | -/TAT | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961376 | TTAGTGGTAAACAGA[-/TAT]TATCCTATTAAGCAC | 9169 |
rs767838621 | snp | G/T | 8.28823e-05 | 0.00643695 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924794 | TGGTGGGGGAGGGGG[G/T]GGTGGTGGTGGTAGT | 9169 |
rs767875557 | snp | C/T | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45919062 | AGTAACACTTCAATA[C/T]GTTTGTAAGGGATTA | 9169 |
rs767888518 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983838 | AATAAAAAGACAACC[C/T]TAAAAGTACATCTGA | 9169 |
rs767905172 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947960 | AGCCTTAAAGGTGTG[A/C]GCCACCACACCTGGC | 9169 |
rs767922914 | snp | A/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45994004 | GTTTCTACTAAAAAT[A/G]AAATTAAAAAAATGA | 9169 |
rs767929574 | snp | C/T | 3.29886e-05 | 0.00406118 | missense | SCAF11 | GRCh38.p7 | 12:45927051 | TAGAAGTTTCTCTTC[C/T]TGGGGACAGTGATTC | 9169 |
rs767956291 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963163 | AACGGTCTAACATAC[C/T]AATTGAAATCCAAAA | 9169 |
rs767960125 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958302 | TACAATGTGTGTCAA[C/G]ACTTCTCTGTCCTTT | 9169 |
rs768008525 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985640 | TTGCAAGGCTACCGA[A/G]AAGATCAAATGAAAA | 9169 |
rs768054176 | snp | G/T | 2.88888e-05 | 0.00380047 | utr-variant-5-prime, missense | SCAF11 | GRCh38.p7 | 12:45964187 | CTTTGGAAAAGGGTT[G/T]CCTATAAGATAAATT | 9169 |
rs768056454 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946798 | CAAGAACCAAAGCTG[A/G]TAAGTATTTTTCAGA | 9169 |
rs768073364 | snp | A/G | 1.65378e-05 | 0.00287552 | missense | SCAF11 | GRCh38.p7 | 12:45926585 | TCTTTCAACTTTTCT[A/G]GATTTCTGGTTCTTG | 9169 |
rs768116095 | snp | C/T | 1.65004e-05 | 0.00287227 | missense | SCAF11 | GRCh38.p7 | 12:45928815 | TTTGCTTCTTTTCTT[C/T]CCCTTCTTGAGTATG | 9169 |
rs768117658 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931790 | TAAAGATAGCTACCA[A/G]TTGGCTAAAATTCAG | 9169 |
rs768141410 | snp | C/T | 3.69385e-05 | 0.00429743 | missense | SCAF11 | GRCh38.p7 | 12:45934231 | TAACAGAAGAAAACA[C/T]ATTGGAGAAAAAATT | 9169 |
rs768160356 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981591 | CATTTCCCCAAGTTA[C/T]TCTAGTTACAGATTA | 9169 |
rs768169156 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945698 | TGCACCACCTTGTCA[C/G]GTTAATTTTTTCTAT | 9169 |
rs768259626 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929945 | AAACAGTTTTTACTC[C/G]CCAAAACTTAACTGT | 9169 |
rs768263047 | snp | G/T | 1.64923e-05 | 0.00287156 | missense | SCAF11 | GRCh38.p7 | 12:45926660 | TCATTTCTATGTTTG[G/T]CAGCAGAATTTGGAT | 9169 |
rs768279773 | snp | C/T | 1.65578e-05 | 0.00287726 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927772 | TGTTGCAATTATTTC[C/T]ACATCTTCAGTTTCA | 9169 |
rs768285235 | snp | A/G | 4.94181e-05 | 0.00497057 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923039 | CTGTGACTTGATGAC[A/G]AAGTATTACCAGAAC | 9169 |
rs768389021 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943332 | AATTCTTAAGTTTTA[A/T]ATTGTACACCATTCT | 9169 |
rs768437570 | snp | A/C | 0.000166847 | 0.00913213 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45992038 | CCGACCGACCGCTTC[A/C]CTGCCGCCTTCCTGC | 9169 |
rs768442581 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | SCAF11 | GRCh38.p7 | 12:45926801 | TTTGCCCATCTTCCC[C/T]TCCACCGGGGAGAGT | 9169 |
rs768444162 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959120 | GAAATCTAGAAAGAT[C/G]ATCCTAACTGCAAAT | 9169 |
rs768453843 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45926958 | CATCTCTATCACTTT[C/T]TCGTTCTCTGCTCTG | 9169 |
rs768520670 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985905 | CTTATTAAGCTCTTA[C/T]CAACACTTGACCCAA | 9169 |
rs768539620 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991716 | TTTCAAAGTCACTGA[C/T]TATTTAACCTCCTAG | 9169 |
rs768548287 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957764 | CATCCTCATCACATA[C/T]ACTGCAGGTTCCATT | 9169 |
rs768564885 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922366 | AGGAATTAGTAGGAG[C/T]TAGCTTTTATTATTT | 9169 |
rs768580761 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973286 | AGAAAAACATTGAAA[A/C]AAAAATATTAAAGGC | 9169 |
rs768614068 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | SCAF11 | GRCh38.p7 | 12:45928380 | AATTAGCAGACTGGT[C/T]TTCTACATGAGTCTG | 9169 |
rs768650109 | in-del | -/AG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923874 | TTTTTTTTTCTAGAC[-/AG]AGTCTTGCTCTGTCA | 9169 |
rs768674926 | snp | A/T | 4.95983e-05 | 0.00497963 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964108 | AAATGAAAAGTTACC[A/T]TCCATGTCTTCATAC | 9169 |
rs768680748 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984438 | CAAATGGCATACAAT[C/T]TCTGTTTGTCTCATT | 9169 |
rs768684569 | snp | A/C | 1.66871e-05 | 0.00288847 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945328 | TCTGTAAACATCAAT[A/C]AAGACAGGAAAGAAT | 9169 |
rs768702099 | snp | C/T | 1.6476e-05 | 0.00287014 | missense | SCAF11 | GRCh38.p7 | 12:45927332 | TGAAATCTAGATCTT[C/T]GAGTACGAGGCTTTT | 9169 |
rs768727780 | snp | C/T | 6.59163e-05 | 0.00574054 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922431 | GGTGGTTCAAAACAA[C/T]GTGCACATACTCCAC | 9169 |
rs768782178 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956195 | TAGATAGCTCCTCTT[-/A]AGAGAGAGAGAAACA | 9169 |
rs768788599 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950505 | ATATTTGGAATCTAC[C/T]TTACACTAATGAATC | 9169 |
rs768804513 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964374 | CACAGTCTTATTGAA[C/T]GGAAAAGCCTTGGCC | 9169 |
rs768812396 | snp | A/T | 1.65261e-05 | 0.0028745 | missense | SCAF11 | GRCh38.p7 | 12:45926526 | CAAAGTTTTTATTCC[A/T]AGAATTTCCTGAATT | 9169 |
rs768870646 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939412 | AGAAATTAAAGAAGT[A/T]TGGCCAGGTGCAGTG | 9169 |
rs768892147 | snp | G/T | 1.80286e-05 | 0.00300233 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933273 | TCAGAATCTCACAAT[G/T]TTAGGTTCAAAAAAA | 9169 |
rs768906562 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965446 | ATGTTAATATGGCAA[A/C]GGCAAGAAATTCATA | 9169 |
rs768924032 | snp | A/T | 1.71652e-05 | 0.00292955 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922611 | AATGTATAATTTATT[A/T]TTTGCCAGTCATACT | 9169 |
rs768968060 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941984 | GACAAGGACAAAGAC[C/T]TTTATGATGATCCAC | 9169 |
rs768984221 | snp | A/G | 1.64822e-05 | 0.00287068 | missense | SCAF11 | GRCh38.p7 | 12:45928157 | CCTCCTTTTTCAAGA[A/G]TATTTTCAGAAATCT | 9169 |
rs768989021 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948828 | AAATTAACTGAGGAT[A/G]TCACAGAAGACTTTA | 9169 |
rs769009960 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989806 | CCCATTCGCGCACTC[A/G]AGAGGTCACGGCGTA | 9169 |
rs769039758 | snp | C/T | 1.6617e-05 | 0.00288239 | missense | SCAF11 | GRCh38.p7 | 12:45951651 | ATAAAAAGACTTACC[C/T]TAACATAACCTTCCA | 9169 |
rs769072101 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975703 | AAACTTTCTTCATAT[C/T]AGTGACAAGGCTGTT | 9169 |
rs769137581 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978573 | CTACAGGAGCACTTG[C/G]GTCAACAGCACTGTA | 9169 |
rs769154448 | snp | A/C | 1.64776e-05 | 0.00287028 | missense | SCAF11 | GRCh38.p7 | 12:45924888 | GGTAGCTGAGGATGA[A/C]TGTTAAATGGATTGC | 9169 |
rs769166927 | snp | A/C | 1.64866e-05 | 0.00287106 | missense | SCAF11 | GRCh38.p7 | 12:45927176 | CGGGATTTTTTCCGG[A/C]CTCTGGCTGACTCAT | 9169 |
rs769188829 | snp | G/T | 3.295e-05 | 0.00405881 | missense | SCAF11 | GRCh38.p7 | 12:45924968 | ATTCATAGGCTGGTG[G/T]TGTGCATTCATTTGT | 9169 |
rs769192866 | snp | C/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991388 | TGAGCGACGTATTAA[C/G]ATCTCGTTTCTACAA | 9169 |
rs769206417 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988831 | TGACTGTTAAAATAT[C/G]TGCAAGCACCAAAAA | 9169 |
rs769233442 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956469 | GTACTTCCAAATTAA[C/T]TGTTCACCTGCAGTC | 9169 |
rs769251406 | snp | G/T | 1.66358e-05 | 0.00288402 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951643 | GTTGCAGAATAAAAA[G/T]ACTTACCTTAACATA | 9169 |
rs769258234 | in-del | -/AGA | 1.64909e-05 | 0.00287144 | cds-indel | SCAF11 | GRCh38.p7 | 12:45926665 | TCTATGTTTGTCAGC[-/AGA]ATTTGGATCATCAGC | 9169 |
rs769294707 | snp | A/G | 1.64789e-05 | 0.0028704 | missense | SCAF11 | GRCh38.p7 | 12:45924868 | CTCCTGTGTGGAGAT[A/G]CAAGGGTAGCTGAGG | 9169 |
rs769306781 | snp | A/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993313 | ATCAGTCCTGTCACA[A/T]AGCAACAGAAACCCA | 9169 |
rs769317830 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959019 | AATAAATGAGTCCTT[C/T]TTTGGTGCTTGATAT | 9169 |
rs769352747 | snp | C/T | 1.64754e-05 | 0.00287009 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924980 | GTGTTGTGCATTCAT[C/T]TGTTGCTGCATTACA | 9169 |
rs769365278 | snp | A/G | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928240 | AACTTCCCCTTCCTC[A/G]CCAACTAGCACAGGA | 9169 |
rs769373024 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972685 | TGTAACATAATATTC[A/G]AAATGTACAGAACAC | 9169 |
rs769395413 | snp | A/G | 3.30573e-05 | 0.00406541 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927646 | TTCGGTCAGCGATTC[A/G]TTCTTTTCTTCTAAA | 9169 |
rs769481334 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969714 | AACAACTAAATTGAT[C/T]AAGTCTCCTATTAGA | 9169 |
rs769570746 | snp | C/T | 1.65594e-05 | 0.0028774 | missense | SCAF11 | GRCh38.p7 | 12:45927755 | TTCCCAAAAGTATCA[C/T]ATGTTGCAATTATTT | 9169 |
rs769579029 | snp | C/T | 0.000138131 | 0.00830942 | intron-variant, missense | SCAF11 | GRCh38.p7 | 12:45974194 | TTTAAAAATACCTTA[C/T]TGCTAAAAATGCTAA | 9169 |
rs769581270 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984213 | ACAGTCCCCCAGTCT[G/T]GACTTTCATGACCTT | 9169 |
rs769583042 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971034 | AAAGTGAAAGGCAAG[C/T]CAGAAATCGTCAGCC | 9169 |
rs769589960 | snp | C/T | 0.000225734 | 0.0106215 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45992015 | CTCCCCACTTTGCCG[C/T]GGCCCCGCCGACCGA | 9169 |
rs769632627 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919861 | TTTGCAAAAGCTAAA[C/T]GGTATAAAACACATT | 9169 |
rs769639871 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950904 | CTATTAACGGCATCA[C/G]TTATGTTTATATTGA | 9169 |
rs769651890 | snp | A/G | 1.65351e-05 | 0.00287528 | missense | SCAF11 | GRCh38.p7 | 12:45926562 | TTCTATTTTCTTCCC[A/G]ATGAGACTCTTTCAA | 9169 |
rs769676106 | snp | A/C | 5.48913e-05 | 0.00523857 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945211 | AATTAAAAAACAACA[A/C]AAAAAAAGGTAGAAT | 9169 |
rs769697374 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936798 | TATCTCATTTAGTGA[A/G]GTATATACATACATC | 9169 |
rs769718399 | snp | C/T | 3.30196e-05 | 0.00406309 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922906 | TATCATATACAGAAT[C/T]ATGAAGGTTGCTCTC | 9169 |
rs769732587 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983342 | CCCCTAGGGCACAGA[A/C]CTAATAGACACATAG | 9169 |
rs769735409 | snp | C/G/T | 7.17043e-05 | 0.0059873 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934399 | ATGGACTAAATAACC[C/G/T]TAAAGTGTTATCATC | 9169 |
rs769738722 | snp | C/T | 4.95135e-05 | 0.00497537 | missense | SCAF11 | GRCh38.p7 | 12:45926636 | TTTTCTGTTATCCAA[C/T]TGGGACAGTCATTTC | 9169 |
rs769781121 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983370 | TAGATATCAACAAAC[C/T]TGGAGTTCAGAACTA | 9169 |
rs769787137 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930609 | CACAAAAATTGTTAC[A/C]CTGGTAAATACGTAC | 9169 |
rs769858027 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947374 | ATGTTAAAATAGGCA[A/C]TGGTTTTAACAGCAA | 9169 |
rs769926282 | in-del | -/T | 3.39403e-05 | 0.00411934 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961860 | CGTTTTCTTCACCTG[-/T]TTAAAGTAAAACAGC | 9169 |
rs769940932 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964035 | TGTGTATTCTGAAAT[A/G]TATACAAGTGGACAG | 9169 |
rs770012135 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988401 | CTAAAAGATGTTACT[G/T]ATGATGAATCAACAG | 9169 |
rs770025518 | snp | A/T | 3.34963e-05 | 0.00409232 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961840 | CAGTGGAAATAGTAT[A/T]ATCTCCGTTTTCTTC | 9169 |
rs770027396 | snp | C/T | | | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926362 | CACAAACTTGAAAGA[C/T]TCACTCCCTGAACTG | 9169 |
rs770027824 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941017 | CCACGTTGCCTCAAT[A/C]TTATTTCTGATCATC | 9169 |
rs770065046 | snp | A/T | 1.64852e-05 | 0.00287094 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922079 | TCAGTAGACACAGGT[A/T]CTTCCAGAGTTTTCT | 9169 |
rs770065622 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971225 | GCAAGGTCACCTACA[C/T]GTTGAAAAAAATTAT | 9169 |
rs770099000 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941549 | CTCTGAATCCCTTGA[C/T]AAACATCTCCCTATC | 9169 |
rs770118606 | snp | A/T | 1.64817e-05 | 0.00287064 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922415 | CATTTATTAAAACAG[A/T]GGTGGTTCAAAACAA | 9169 |
rs770138421 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976423 | TTTCTGCACCTAATT[C/T]ATAAGTTAAACTTTA | 9169 |
rs770191433 | snp | A/C | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975506 | TTGCACTTTTATGTT[A/C]TGGAGATGGCTTCTT | 9169 |
rs770213942 | snp | C/T | 1.64893e-05 | 0.0028713 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928045 | TTCAGATGTTAAACA[C/T]GTAGGAAAATCATTT | 9169 |
rs770275844 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954918 | CCGTTTCAAAAAACA[G/T]TTCTGAGTAAGATTC | 9169 |
rs770299084 | snp | A/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920147 | AATACCATATTACAA[A/T]TGCCCAGAAATGTAG | 9169 |
rs770300050 | snp | A/G | 1.65127e-05 | 0.00287334 | missense | SCAF11 | GRCh38.p7 | 12:45926999 | TTTTCTCCTGGGGAA[A/G]AATCTTTCACTCTTG | 9169 |
rs770330847 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952959 | AGTAGAGCAGATTGT[A/G]TATGGTCCTTGATCA | 9169 |
rs770375171 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968335 | CCAAGCTAAAATATC[G/T]TTTTAGTCTGTGACC | 9169 |
rs770376436 | snp | A/G | 1.64977e-05 | 0.00287203 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927076 | TGATTCAGATCTTCT[A/G]CTTTCCCTAGTAGTA | 9169 |
rs770404254 | snp | C/G | 1.64825e-05 | 0.00287071 | missense | SCAF11 | GRCh38.p7 | 12:45928119 | AAAGTCCAGATATCT[C/G]GTCTTGCTTTTCCAA | 9169 |
rs770415745 | snp | G/T | 1.65031e-05 | 0.00287251 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926961 | CTCTATCACTTTCTC[G/T]TTCTCTGCTCTGGGA | 9169 |
rs770430033 | snp | C/T | 5.06718e-05 | 0.00503322 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945361 | AGAAAAAAACTGTCA[C/T]TTTGCTCACTTATTT | 9169 |
rs770433457 | snp | C/T | 3.38501e-05 | 0.00411387 | missense | SCAF11 | GRCh38.p7 | 12:45924742 | CCTGCAATTGCTTTC[C/T]ATCTGGTTGTGAAGC | 9169 |
rs770456141 | snp | A/G | 1.69983e-05 | 0.00291528 | missense | SCAF11 | GRCh38.p7 | 12:45948483 | AGACCTGTTTCTCAA[A/G]TGAGTTTTCATTTTT | 9169 |
rs770497973 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957941 | TTTGTCACCCAGGCT[A/G]AAGTGCAGTGGCATA | 9169 |
rs770545539 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919742 | ATCAGACATGGAACA[C/T]ACACTTGTTACTGTC | 9169 |
rs770545930 | snp | C/T | 1.64768e-05 | 0.00287021 | missense | SCAF11 | GRCh38.p7 | 12:45928629 | CAGCTGAAGAGGGAA[C/T]ACTTAAAGATGGATT | 9169 |
rs770575599 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923664 | TGTCAGGATTCTATT[C/T]ATTTTATTTTATTTT | 9169 |
rs770596931 | snp | C/T | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918693 | GCCTGGGCAACAGAG[C/T]GAGACTCCATCTCAA | 9169 |
rs770631371 | snp | A/G | 1.64789e-05 | 0.0028704 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924860 | GAGGGGCACTCCTGT[A/G]TGGAGATGCAAGGGT | 9169 |
rs770649857 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933686 | TTTTTCTTGGTACCT[C/T]GCCAAGTTCTAAAAT | 9169 |
rs770653180 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943879 | CATTATAATTTTAAA[-/AT]AGCTATCCAATCTAA | 9169 |
rs770689641 | snp | C/T | 1.64757e-05 | 0.00287012 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928720 | GGCTGTTTCAGCTCT[C/T]GTGTTACGTGTAGAC | 9169 |
rs770694271 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970830 | TAAAATCAGTTTCCT[A/G]TATCAATCCAGAAAG | 9169 |
rs770712333 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983081 | TGATAATAAAGTGCA[A/G]AAAGTTAATGTTCTT | 9169 |
rs770748700 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947128 | GTATTCTGATGAAAA[A/G]TACTAATGAATCATA | 9169 |
rs770774462 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977165 | GCATTATCCTCATGC[-/A]AAAAAAAAAATAGTA | 9169 |
rs770782081 | snp | A/G | 1.64792e-05 | 0.00287042 | missense | SCAF11 | GRCh38.p7 | 12:45927503 | TTTACAGATGGTTCA[A/G]CTTCAGATTCATTTT | 9169 |
rs770783979 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988926 | TATAAATTCAGATTA[C/T]CCGATAGGATAATAT | 9169 |
rs770788182 | in-del | -/GAG | 1.6507e-05 | 0.00287284 | cds-indel | SCAF11 | GRCh38.p7 | 12:45927018 | CTTTCACTCTTGGCT[-/GAG]ATCTTTTGTTCTCTC | 9169 |
rs770803743 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962240 | AAAAACAAATGCTAA[C/T]ACAAACTCTTCCACA | 9169 |
rs770826088 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972967 | ATATATAGATATATA[G/T]ATAGATATATAGATA | 9169 |
rs770871909 | snp | C/T | 4.94923e-05 | 0.0049743 | missense | SCAF11 | GRCh38.p7 | 12:45926402 | CCTGAGAGGGGTTTT[C/T]GATTTTGCCACCGAT | 9169 |
rs770883010 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946043 | CATGACTGACTGGCT[A/G]TTGAGCCACGCAGAC | 9169 |
rs770917982 | in-del | -/ATC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955072 | AAACTACTGCCATAT[-/ATC]ATCACAATCTATATA | 9169 |
rs770983947 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960782 | AAAATTTAAGCAAAA[C/T]ATAGCGCTTTGAAAA | 9169 |
rs771017706 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | SCAF11 | GRCh38.p7 | 12:45927306 | TGGGTGACCAAGTTG[C/T]AGATGGAGAATGAAA | 9169 |
rs771031513 | snp | A/T | 1.65307e-05 | 0.0028749 | missense | SCAF11 | GRCh38.p7 | 12:45926540 | CAAGAATTTCCTGAA[A/T]TTTCATTTCTATTTT | 9169 |
rs771076477 | snp | C/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975448 | TAGCTAGGTCTTCTG[C/G]ATAACCTGATGCAGC | 9169 |
rs771080963 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930008 | TTAATATATTTTTTA[-/T]GTTATGTGTTACATA | 9169 |
rs771112707 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923956 | CCTGGGTTCAAGCAA[C/T]TCTCCTGCCTCAACC | 9169 |
rs771166143 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939700 | CTGGGCAACAAGACC[A/G]AAACTCCATCTCAAA | 9169 |
rs771181082 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | SCAF11 | GRCh38.p7 | 12:45927378 | TATCTTTTGGGCTTT[C/T]AGATGGTTGAGAAAC | 9169 |
rs771183722 | snp | C/T | 3.29701e-05 | 0.00406005 | missense | SCAF11 | GRCh38.p7 | 12:45926207 | GAAGAATTTCTGCCT[C/T]GTCGTGAGTAGTAGT | 9169 |
rs771200355 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941707 | AGGTCAAGACCTTGT[A/C]GTCAACCCTGACTTC | 9169 |
rs771235077 | snp | C/T | 1.65241e-05 | 0.00287433 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922056 | CCCCATTTCAGCCTA[C/T]GTTTTTTTCAGTAGA | 9169 |
rs771255962 | in-del | -/C | 2.99927e-05 | 0.00387239 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964077 | CTGTTTTGCTTTCAA[-/C]AAACAAACTTTATAA | 9169 |
rs771272957 | snp | C/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974696 | ACCACACCTGTAATA[C/G]TTACTTCCTCCACAC | 9169 |
rs771274937 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988022 | ATAGCAAGAGAATGA[C/T]ACTGGATATTTTAAC | 9169 |
rs771288903 | snp | C/T | 1.74928e-05 | 0.00295738 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961680 | TAGGAAATTAAAATA[C/T]ATTAATGTGTCAGAC | 9169 |
rs771318774 | snp | A/T | 1.66131e-05 | 0.00288206 | missense | SCAF11 | GRCh38.p7 | 12:45927935 | TCAGTAATTTCTACT[A/T]GGGAACTCTCTGTTA | 9169 |
rs771329968 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987347 | ACAGACTGAGACTTG[C/T]TTAGTCTAAAGTTTC | 9169 |
rs771339839 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945816 | GGAATTACAGGTGTA[A/T]GCTACCATGCCTGGC | 9169 |
rs771383322 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986056 | CAAAGTTTTTTAAAT[A/G]TTAGAGGTCATTGTG | 9169 |
rs771392088 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972463 | AGTGGTGTGTCACTG[C/T]AGTCCCAGCTAATCA | 9169 |
rs771406614 | snp | C/T | 3.29489e-05 | 0.00405874 | missense | SCAF11 | GRCh38.p7 | 12:45926838 | CTCTGTCAATTCTAC[C/T]AAATGATGAACTCTT | 9169 |
rs771424510 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966904 | AAAAATATTAAGGTT[A/G]GAGTTAACTCAATGT | 9169 |
rs771498351 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45975843 | TGTCTTATATGGGCG[A/C]TCTTCGTGGTGCCCC | 9169 |
rs771517538 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980495 | TACAGTGATACTGTC[A/G]TTACCCCCATTTTAT | 9169 |
rs771534542 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931253 | ATTTCCTTCTTTTTG[C/T]GGCAGAATAATATTC | 9169 |
rs771538193 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939874 | CTATATCATGGTTTC[G/T]GTTCAGTGTAACTGG | 9169 |
rs771590649 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933320 | AGAATAGCAGTCGTT[C/T]TTGTACCTGGCATTA | 9169 |
rs771591429 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929836 | GTGAGAACACTTTAC[A/G]TCCACTCTCTAGCAA | 9169 |
rs771594125 | snp | A/G | 6.58957e-05 | 0.00573964 | missense | SCAF11 | GRCh38.p7 | 12:45926811 | TTCCCTTCCACCGGG[A/G]AGAGTAACTATCTCT | 9169 |
rs771648682 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969338 | CCCTTCTTTCCTTCT[A/G]TTTTTTTTCTTCCAA | 9169 |
rs771663996 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925980 | ATGTAGATAAACGTA[C/T]GTGTATATATATTTA | 9169 |
rs771679383 | snp | C/T | 3.34314e-05 | 0.00408835 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922037 | TAATGTCCTTGACAG[C/T]GTTCCCCATTTCAGC | 9169 |
rs771688747 | snp | C/T | 8.25471e-05 | 0.00642392 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923135 | ATGTTATTACTTACA[C/T]GAGAAGAACTAGGAA | 9169 |
rs771774581 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993606 | GGTGAAACCCCATCT[C/T]TACTGAAAATACAAA | 9169 |
rs771777187 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932202 | TATTCTAAAATTCCT[C/T]GACCTGGTGATGGCT | 9169 |
rs771849366 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982932 | GTAGACTTGGAGACA[C/T]AGGATACAGAAGATG | 9169 |
rs771865643 | snp | G/T | 1.67206e-05 | 0.00289137 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945340 | AATAAAGACAGGAAA[G/T]AATTAAGAAAAAAAC | 9169 |
rs771904348 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981739 | GGTTAAGGTTGCAGG[C/G]AACTATGGCCATCCC | 9169 |
rs771940224 | snp | A/G | | | intron-variant, missense | SCAF11 | GRCh38.p7 | 12:45974212 | CTAAAAATGCTAACA[A/G]TCATCTCAGCAAGGC | 9169 |
rs771955431 | snp | A/G | 1.68903e-05 | 0.00290601 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45948460 | GCTTTTAGAATTTTC[A/G]TGACAGGAGACCTGT | 9169 |
rs771966045 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932040 | TACCAAAGTGTGTGC[-/AT]ATATATATATATATA | 9169 |
rs771970712 | snp | C/T | 1.64808e-05 | 0.00287057 | missense | SCAF11 | GRCh38.p7 | 12:45927473 | GAATTTTCATTCATT[C/T]GTTTAAGATCAGCAT | 9169 |
rs771980556 | snp | A/G | | | intron-variant, synonymous-codon | SCAF11 | GRCh38.p7 | 12:45960180 | AGAGAAACCTGGAAC[A/G]TGTACATCAGGGTAA | 9169 |
rs771999275 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987132 | TTGGGAGGCCAAGGC[A/G]GGATGATTACTTAGC | 9169 |
rs772002831 | snp | A/G | 6.72518e-05 | 0.00579839 | synonymous-codon, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961847 | AATAGTATTATCTCC[A/G]TTTTCTTCACCTGTT | 9169 |
rs772024177 | snp | A/G/T | 3.30405e-05 | 0.0040644 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922897 | TTTCTCCTTTATCAT[A/G/T]TACAGAATTATGAAG | 9169 |
rs772066304 | snp | C/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991790 | TGCCCTCAGTGTCCC[C/G]CATCTACCAGCTGAC | 9169 |
rs772090466 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923841 | AATGCATCACCGCGC[C/G]TGGCTAATTTTTGTA | 9169 |
rs772137064 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973558 | AGTCAAGCTACTGAA[A/T]GTTACAAAGGAAAAC | 9169 |
rs772143580 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922626 | ATTTGCCAGTCATAC[C/T]GCTCTCACAAAATCC | 9169 |
rs772193980 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929835 | AGTGAGAACACTTTA[C/T]GTCCACTCTCTAGCA | 9169 |
rs772194073 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931194 | GCCTGCCTTATTCAC[C/T]TAGCCTAATGTCCTC | 9169 |
rs772200484 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986003 | CCCTCTACTTCTCTG[A/G]TCTTCACGGTATTCT | 9169 |
rs772227064 | snp | C/T | 3.29451e-05 | 0.00405851 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923013 | ATTTTACAGCAGCAT[C/T]AGAGGCTTTGCTGTG | 9169 |
rs772262446 | snp | C/T | 1.64874e-05 | 0.00287113 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928261 | TAGCACAGGAAGATC[C/T]TGAGCACAAGACTCA | 9169 |
rs772266961 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965688 | TCCAAATATGCATTT[A/G]TATCTACGCACAAGA | 9169 |
rs772277567 | snp | A/G | 1.80748e-05 | 0.00300618 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951773 | CAAATGTTTCTTTAG[A/G]TCAAAATTATAAATA | 9169 |
rs772312598 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952518 | GTTGCTACTCTTTTT[C/T]AAATTGAGTTATAGG | 9169 |
rs772344423 | snp | G/T | 1.64814e-05 | 0.00287061 | missense | SCAF11 | GRCh38.p7 | 12:45928346 | CTTTCTTCTATTTGC[G/T]CATTGCAACTTTTCA | 9169 |
rs772353129 | snp | C/G | 1.97085e-05 | 0.00313909 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925092 | ATCAAAAGAAAAAAA[C/G]CTTGTGAAAAAAATC | 9169 |
rs772375490 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921225 | TGACCTCAGGTGATC[C/T]GCCACCTCGGCCTCC | 9169 |
rs772388026 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929568 | AGATGTTACTTCTAA[A/G]GATCTATGGTTTGGA | 9169 |
rs772398080 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45937099 | CATATCTGGACACCT[A/G]TGCTCTACTATTACG | 9169 |
rs772406556 | snp | A/G | 1.64912e-05 | 0.00287147 | missense | SCAF11 | GRCh38.p7 | 12:45927198 | CTGACTCATTCTTAG[A/G]AGATGGTGATTGAGA | 9169 |
rs772433229 | snp | C/T | 4.94262e-05 | 0.00497098 | missense | SCAF11 | GRCh38.p7 | 12:45924989 | ATTCATTTGTTGCTG[C/T]ATTACATTCATTTGC | 9169 |
rs772491621 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965644 | ATATTCCTTCCTGAA[C/T]TGATGCAAGACATAA | 9169 |
rs772554060 | in-del | -/CT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946136 | TGATTAGTTTCACTC[-/CT]CACTCAGTTACCATT | 9169 |
rs772561819 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978119 | TTTACCATGAGAGTC[C/T]GAAAAATCATCAAAT | 9169 |
rs772562398 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956530 | GTTCTTTCAAGACAG[C/T]CTTTGTCAATCCATA | 9169 |
rs772602405 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981733 | CCAGGAGGTTAAGGT[G/T]GCAGGGAACTATGGC | 9169 |
rs772619390 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991132 | CCTGAAATGCAGCCT[A/G]TGGAGTGAAGAGTCG | 9169 |
rs772625658 | snp | C/G | 1.65531e-05 | 0.00287686 | missense | SCAF11 | GRCh38.p7 | 12:45927795 | CAGTTTCAACATGCC[C/G]AAGCAATTGAACCTC | 9169 |
rs772633395 | in-del | -/CAA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953521 | GTACTGCAGCCTAGG[-/CAA]CAACAGAGTGAGATC | 9169 |
rs772653371 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942128 | AATGTGTTTATCAAC[C/T]GTTTATGTTATCTGT | 9169 |
rs772679605 | snp | G/T | 1.78465e-05 | 0.00298712 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961650 | ATCAACTCTTTAGGT[G/T]AAATGAAATCATGCT | 9169 |
rs772696373 | snp | C/T | 3.5322e-05 | 0.00420235 | missense | SCAF11 | GRCh38.p7 | 12:45931515 | CTTTACCAAAATGTT[C/T]GAAAGATATGGTACT | 9169 |
rs772700904 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988891 | GAACTGTTTTTAAAA[A/C]ACTCACATTGCATAA | 9169 |
rs772745510 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940239 | TATGACCTTTAACCT[A/G]AAGGAAAAAAAAATC | 9169 |
rs772798482 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955167 | AGACTCAGCCATCAT[A/G]ATTTTTTTTTTAAAC | 9169 |
rs772840333 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932232 | TCTTCAAAGTTCTCA[A/G]TGTCCCTAGAGACCT | 9169 |
rs772857844 | snp | A/G | 5.04053e-05 | 0.00501997 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945357 | ATTAAGAAAAAAACT[A/G]TCATTTTGCTCACTT | 9169 |
rs772867798 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969363 | TTCCAAAGTCTGTTT[C/G]TTTCTGCTGTTACAA | 9169 |
rs772929293 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968528 | ATTAAAGCTTGGAAT[C/T]TAAAATTTAAAAAAA | 9169 |
rs772933491 | snp | A/G | 1.648e-05 | 0.0028705 | missense | SCAF11 | GRCh38.p7 | 12:45928400 | ACATGAGTCTGCACA[A/G]TACAAATGTTACTAC | 9169 |
rs773011569 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | SCAF11 | GRCh38.p7 | 12:45926286 | ATGTCCATCCAGATC[C/T]ATCTGCTGGTGTATC | 9169 |
rs773094584 | snp | C/T | 1.68638e-05 | 0.00290373 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961851 | GTATTATCTCCGTTT[C/T]CTTCACCTGTTAAAG | 9169 |
rs773099000 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983377 | CAACAAACCTGGAGT[C/T]CAGAACTATGGGTAG | 9169 |
rs773131692 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967430 | GGGAGGAGCGTCTGA[C/G]ATCAGGAGTTCGAGA | 9169 |
rs773131801 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981869 | AATAATGTAAATAAT[C/T]GTGCACACCAATTAA | 9169 |
rs773149302 | snp | C/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993684 | CTCAGGAGGCTGAGG[C/G]AGGAGAATCACTTGA | 9169 |
rs773165261 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938680 | CATGAAACACTAATC[C/T]GAAAGGATGTTTCAT | 9169 |
rs773176850 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980735 | ATAGCAGCTAACTCT[A/C]TGTTCCATTCTCTTA | 9169 |
rs773183950 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930657 | AGCTATGATTTAATA[C/T]TGTATCTTTACAGCT | 9169 |
rs773185186 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986252 | TCTACCTGAAAGCTC[C/T]AAAGGTACTTTAAGC | 9169 |
rs773193739 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973653 | AATCACCGGTGATTT[C/T]TTATCAGAAACCATG | 9169 |
rs773200727 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943676 | TCAAATCAGTCCAGG[C/T]TGGTCAGTGAAGACA | 9169 |
rs773206389 | snp | G/T | 1.64917e-05 | 0.00287151 | missense | SCAF11 | GRCh38.p7 | 12:45926385 | CTGAACTGTTTGAAT[G/T]CCCTGAGAGGGGTTT | 9169 |
rs773212780 | in-del | -/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985657 | AGATCAAATGAAAAT[-/G]TATGTAAAATGTCTA | 9169 |
rs773252949 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986015 | CTGATCTTCACGGTA[C/T]TCTCTGGGAGCTCAC | 9169 |
rs773292405 | snp | A/G | 1.64925e-05 | 0.00287158 | missense | SCAF11 | GRCh38.p7 | 12:45927201 | ACTCATTCTTAGGAG[A/G]TGGTGATTGAGACTT | 9169 |
rs773317476 | snp | C/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974508 | ACTAAGTTTATATAC[C/T]ATTTTAACAATGTTC | 9169 |
rs773328127 | in-del | -/AAGA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45952641 | CTGTGCATCAACTCT[-/AAGA]GTTTCTCTGATAAAA | 9169 |
rs773339022 | snp | C/T | 4.94311e-05 | 0.00497123 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45925004 | CATTACATTCATTTG[C/T]GGTTGCATCATATTT | 9169 |
rs773389902 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922628 | TTGCCAGTCATACTG[C/G]TCTCACAAAATCCCA | 9169 |
rs773411057 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936481 | GGTTAATAATGTCTT[C/T]GTTTTCTCTTTTCCT | 9169 |
rs773442888 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921277 | GTGAGCCATCATGCC[C/T]GGCCGAAAGTCAACA | 9169 |
rs773497043 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45990100 | GCGGCGGCGGCCCAG[G/T]GCCGGGCCGAGCCTC | 9169 |
rs773537491 | snp | A/G | 0.000105232 | 0.00725292 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45931516 | TTTACCAAAATGTTC[A/G]AAAGATATGGTACTT | 9169 |
rs773574641 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972336 | ATGTAATCCCAGCAC[-/T]TTTAAGAGGTCAAGA | 9169 |
rs773574998 | snp | C/G | 2.01234e-05 | 0.00317195 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925096 | AAAGAAAAAAAGCTT[C/G]TGAAAAAAATCATGT | 9169 |
rs773591216 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951056 | GTTTTTTTGTTTTTT[A/C]AGGTAAGCAAAAAAT | 9169 |
rs773625389 | snp | A/T | 1.66123e-05 | 0.00288199 | missense | SCAF11 | GRCh38.p7 | 12:45927927 | CTTTATGTTCAGTAA[A/T]TTCTACTAGGGAACT | 9169 |
rs773638755 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964622 | CAGTGAGCCCAGATC[A/G]CGCCACTGCACTCCA | 9169 |
rs773640716 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978184 | ACTGTAAACAGTAGC[A/G]TATGTCCTTTGATAA | 9169 |
rs773654165 | snp | A/G | 1.65151e-05 | 0.00287355 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928003 | TAAGTCACTTAGGGG[A/G]CAAGATACAGGTTGG | 9169 |
rs773668416 | in-del | -/AAGCCTAC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45933650 | AGTTCAGCTTTTCAA[-/AAGCCTAC]AAGCCTACTTAGACA | 9169 |
rs773692405 | snp | C/T | 4.96364e-05 | 0.00498154 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951795 | TTATAAATACAATTA[C/T]AAATTTTCCATAAAA | 9169 |
rs773693683 | in-del | -/AAGT | 1.70069e-05 | 0.00291602 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961864 | TTTCTTCACCTGTTA[-/AAGT]AAAACAGCCATATGT | 9169 |
rs773715585 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968341 | TAAAATATCTTTTTA[A/G]TCTGTGACCCCTAAT | 9169 |
rs773746902 | in-del | -/TTTACCAAAATG | 2.00415e-05 | 0.00316549 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931501 | AATGATTTCACAAAC[-/TTTACCAAAATG]TTCGAAAGATATGGT | 9169 |
rs773749774 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924495 | TGTTCAGATATAAGT[-/A]ACAGCATATATGTAG | 9169 |
rs773776931 | snp | C/T | 1.6537e-05 | 0.00287545 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926572 | TTCCCAATGAGACTC[C/T]TTCAACTTTTCTGGA | 9169 |
rs773893742 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953144 | TCAGACTGGAAGAAG[A/C]CAGTTCAGCCTACTT | 9169 |
rs773894339 | snp | C/T | 1.65559e-05 | 0.00287709 | missense | SCAF11 | GRCh38.p7 | 12:45927777 | CAATTATTTCTACAT[C/T]TTCAGTTTCAACATG | 9169 |
rs773916257 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45931994 | TAATTCAACATAAAA[C/T]GCAGACTTTAAGCGT | 9169 |
rs773933952 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45930135 | AAGTTTATATCATTT[G/T]TTTACAAGATGAATC | 9169 |
rs773946664 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967372 | TAATGGCCAGGTGCC[A/G]GTGGCTCACGCAAGT | 9169 |
rs773958554 | snp | C/T | 1.64991e-05 | 0.00287215 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923129 | GTACTCATGTTATTA[C/T]TTACATGAGAAGAAC | 9169 |
rs773980839 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989058 | CCAAAATAGTGACAT[A/G]ATCAAGCCAACTGCC | 9169 |
rs773987259 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943408 | AGAGTAAGAAGAGTA[A/G]GTACAATAAGAAATT | 9169 |
rs773997998 | snp | C/T | 1.64746e-05 | 0.00287002 | missense | SCAF11 | GRCh38.p7 | 12:45926807 | CATCTTCCCTTCCAC[C/T]GGGGAGAGTAACTAT | 9169 |
rs774041979 | snp | C/T | 1.64928e-05 | 0.00287161 | missense | SCAF11 | GRCh38.p7 | 12:45926661 | CATTTCTATGTTTGT[C/T]AGCAGAATTTGGATC | 9169 |
rs774052440 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954085 | TTTGTGACACTAAGA[G/T]CCAAAGAAAGTCACG | 9169 |
rs774063785 | snp | C/G | 0.000209446 | 0.0102313 | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991841 | GCCCTTGTCCTGCTT[C/G]CGGCTCCCGCAGGAC | 9169 |
rs774078354 | snp | C/T | 1.68655e-05 | 0.00290387 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45934465 | ATTTATCTTTATTGC[C/T]GCATTTTTCTTTCCT | 9169 |
rs774080858 | snp | C/T | 1.6473e-05 | 0.00286988 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923048 | GATGACGAAGTATTA[C/T]CAGAACTTGGTCCCT | 9169 |
rs774083162 | snp | A/C/T | 4.94404e-05 | 0.00497173 | missense | SCAF11 | GRCh38.p7 | 12:45928388 | GACTGGTTTTCTACA[A/C/T]GAGTCTGCACAGTAC | 9169 |
rs774086445 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980670 | CATCATATCCTTACA[A/G]TATTTATGTAACTAA | 9169 |
rs774101580 | snp | C/G | 1.64765e-05 | 0.00287019 | missense | SCAF11 | GRCh38.p7 | 12:45927333 | GAAATCTAGATCTTC[C/G]AGTACGAGGCTTTTT | 9169 |
rs774109483 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945779 | CTCAAGTGATCCTCC[C/T]GCCTTGGCCTCCCTA | 9169 |
rs774129512 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920900 | CCTAACAGCAATTCT[C/T]GAATTGGCACAAATA | 9169 |
rs774148198 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979526 | TTTGCACAAATGCTG[-/A]AAGTTACTCTTTCGT | 9169 |
rs774157170 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959183 | CTGTGGCACAAGAAT[C/T]GCTTGGCCTGGGAGG | 9169 |
rs774210664 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973337 | ACCAAAAACCCAACA[C/T]TCACATCAAGAATGC | 9169 |
rs774242572 | snp | G/T | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960417 | CCAAAGCAAAATCTC[G/T]AAAAAAATTTAACCA | 9169 |
rs774246994 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920127 | TTAAAAATATATACC[A/G]GTAGAATACCATATT | 9169 |
rs774266732 | snp | C/G | 1.66999e-05 | 0.00288958 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945219 | AACAACAAAAAAAAA[C/G]GTAGAATCCACAAGC | 9169 |
rs774279225 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993474 | TGTAAATATACTGGA[C/T]TGAAAAACATGGTTC | 9169 |
rs774288554 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928486 | TGTTTCTTCATCTAC[C/T]GAATCATTGGAAGAT | 9169 |
rs774323720 | in-del | -/TTTTTGGAGACCGAGACTGAGATTGCCTCCTTTCTCTTGCAATATCCT | 1.64977e-05 | 0.00287203 | cds-indel | SCAF11 | GRCh38.p7 | 12:45927096 | CCCTAGTAGTATCCC[lengthTooLong]TTTTTGGGGACTGAG | 9169 |
rs774335979 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991725 | CACTGATTATTTAAC[C/T]TCCTAGTTTCTCTTC | 9169 |
rs774347044 | snp | A/C | | | missense | SCAF11 | GRCh38.p7 | 12:45927366 | TTTTATCTATGGTAT[A/C]TTTTGGGCTTTCAGA | 9169 |
rs774379543 | snp | A/T | 3.29669e-05 | 0.00405984 | missense | SCAF11 | GRCh38.p7 | 12:45928158 | CTCCTTTTTCAAGAA[A/T]ATTTTCAGAAATCTC | 9169 |
rs774382524 | snp | C/G | 1.64781e-05 | 0.00287033 | missense | SCAF11 | GRCh38.p7 | 12:45927408 | CAGTTTCAACCTTTT[C/G]ATCCGCAAGATCAGA | 9169 |
rs774388760 | snp | A/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921128 | GCTGGGATTACAGGC[A/G]CCCACCACCACGCCT | 9169 |
rs774394444 | snp | A/G | 2.2871e-05 | 0.00338156 | synonymous-codon, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964120 | ACCTTCCATGTCTTC[A/G]TACTTCTTATCTCCC | 9169 |
rs774404476 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971313 | ACATTCCAAAATATA[C/T]CAAAAGTGAGATCAA | 9169 |
rs774468331 | snp | C/T | 1.80227e-05 | 0.00300184 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933096 | TTGTTCATGTTAGCA[C/T]GTAAACACCTGAGTA | 9169 |
rs774484075 | snp | A/T | 4.11091e-05 | 0.00453353 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934130 | AAGTTAATAATTATT[A/T]AACATCAAGTATAAA | 9169 |
rs774530478 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936963 | GTTGATGACACTCTG[C/T]AACCCCAATCCTCTA | 9169 |
rs774580709 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983601 | CAGAGTTAGCTGCTA[C/T]TACCACTGGACTTAG | 9169 |
rs774585555 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45950568 | TTGGAAAAATGGAGA[A/G]TATGTCTTCAGGAAA | 9169 |
rs774585638 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45935450 | CTGTATCTAAAAGAT[A/G]ATACGCTGATTTTTT | 9169 |
rs774605441 | in-del | -/T | 4.08705e-05 | 0.00452035 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964214 | AATTATAATAGAGAA[-/T]TTTATGTTTGCCTTC | 9169 |
rs774613569 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962831 | AAGAAACAAATACAA[A/G]TCCTCTGGAGGAAAG | 9169 |
rs774633736 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958116 | CACCATGTTGCCCAG[A/G]CTGGTCTTAAACTCC | 9169 |
rs774655592 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941993 | AAAGACCTTTATGAT[A/G]ATCCACTTCTGCTCA | 9169 |
rs774666788 | snp | C/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975713 | CATATCAGTGACAAG[C/G]CTGTTTGGTCTAATT | 9169 |
rs774696203 | in-del | -/TATC | 1.64806e-05 | 0.00287054 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45922465 | AGCCATAACTTACTT[-/TATC]TACTGCTTTCCGTAC | 9169 |
rs774752372 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45964395 | AGCCTTGGCCGTGCA[C/T]GGTGGCTCACGCCTG | 9169 |
rs774779692 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45948885 | TTAAAGGATAGTTAG[A/G]AATTGGTCTAAGAAA | 9169 |
rs774786291 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989811 | TCGCGCACTCGAGAG[A/G]TCACGGCGTAGTAAA | 9169 |
rs774829891 | snp | G/T | 1.64906e-05 | 0.00287142 | missense | SCAF11 | GRCh38.p7 | 12:45927192 | CTCTGGCTGACTCAT[G/T]CTTAGGAGATGGTGA | 9169 |
rs774837842 | snp | C/T | 1.66161e-05 | 0.00288232 | missense | SCAF11 | GRCh38.p7 | 12:45951652 | TAAAAAGACTTACCT[C/T]AACATAACCTTCCAA | 9169 |
rs774845862 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976227 | AAGTAGACTAAAATT[C/T]TAAGTATGTATAATT | 9169 |
rs774848735 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980595 | ACCATTGACACTAAA[C/G]GGCCTAATACACAAA | 9169 |
rs774851264 | in-del | -/AC | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960262 | ATCTACTTATTACAT[-/AC]ACATTATAATTTTCT | 9169 |
rs774862119 | snp | C/G | 1.65007e-05 | 0.00287229 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928816 | TTGCTTCTTTTCTTC[C/G]CCTTCTTGAGTATGT | 9169 |
rs774863988 | snp | A/G | 3.31686e-05 | 0.00407225 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927676 | AGATTTTTCCAATTT[A/G]GTGTTCAGAAGATTA | 9169 |
rs774894926 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924455 | GGCTTATAATTTGGT[A/T]TACTTAATATGAATA | 9169 |
rs774899627 | snp | C/T | 4.94385e-05 | 0.0049716 | missense | SCAF11 | GRCh38.p7 | 12:45927546 | ATGAATCACACTCCA[C/T]AGGTATCATTTCATT | 9169 |
rs774904302 | in-del | -/CA | | | upstream-variant-2KB, splice-donor-variant | SCAF11 | GRCh38.p7 | 12:45991882 | TCCCCGCGCGCGGCT[-/CA]CCCAGGTCCCAGTCG | 9169 |
rs774912568 | snp | A/T | 1.64765e-05 | 0.00287019 | missense | SCAF11 | GRCh38.p7 | 12:45924892 | GCTGAGGATGAATGT[A/T]AAATGGATTGCGTTG | 9169 |
rs774968549 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965891 | AAAACTAACCATAAA[A/G]GCAGAAGAAACTTAG | 9169 |
rs775019543 | snp | A/C | 1.64749e-05 | 0.00287005 | missense | SCAF11 | GRCh38.p7 | 12:45928735 | TGTGTTACGTGTAGA[A/C]CTCCTTGTAGGAGTT | 9169 |
rs775028037 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976512 | AGTTTCAGGCATCTA[C/T]TTGAAATATATCCCA | 9169 |
rs775150943 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991407 | TCGTTTCTACAAAAA[A/G]TAAAATTAACCGGCC | 9169 |
rs775154051 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45943295 | GCCCAAAAATATTAA[A/G]TGGAAAATTCCAGAT | 9169 |
rs775155934 | snp | A/G | 1.64852e-05 | 0.00287094 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928267 | AGGAAGATCTTGAGC[A/G]CAAGACTCAGAAGAT | 9169 |
rs775181949 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971172 | TCTTCATTTAATGTA[C/G]CATCATCTCCTTAAC | 9169 |
rs775233107 | snp | A/G | 3.29696e-05 | 0.00406001 | missense | SCAF11 | GRCh38.p7 | 12:45928280 | GCACAAGACTCAGAA[A/G]ATGAAGATCCTACTC | 9169 |
rs775239824 | snp | C/G | 2.20175e-05 | 0.00331787 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964143 | TATCTCCCATATTTA[C/G]GGTACATACAGTTTT | 9169 |
rs775352718 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942379 | ACAAAAAAGAAAAAA[C/G]CCACCTAAATAGTCA | 9169 |
rs775371205 | snp | C/T | 1.65072e-05 | 0.00287286 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922908 | TCATATACAGAATTA[C/T]GAAGGTTGCTCTCAA | 9169 |
rs775388334 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45957035 | TCACTCCAACCCACA[C/G]TAAGGATGAAGATGG | 9169 |
rs775434793 | snp | C/T | 1.64982e-05 | 0.00287208 | missense | SCAF11 | GRCh38.p7 | 12:45927216 | ATGGTGATTGAGACT[C/T]CCTGCTTTCTTTCCC | 9169 |
rs775474355 | in-del | -/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932254 | AGAGACCTGTTAAGA[-/C]CCCCCTCCTTCAAAT | 9169 |
rs775494659 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932042 | CCAAAGTGTGTGCAT[-/AT]ATATATATATATATG | 9169 |
rs775499255 | snp | C/T | 6.71175e-05 | 0.0057926 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961842 | GTGGAAATAGTATTA[C/T]CTCCGTTTTCTTCAC | 9169 |
rs775509217 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954928 | AAACAGTTCTGAGTA[A/G]GATTCCCCCCCTTTT | 9169 |
rs775515769 | snp | C/T | 1.80514e-05 | 0.00300422 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933091 | CTATCTTGTTCATGT[C/T]AGCATGTAAACACCT | 9169 |
rs775527608 | snp | A/G | 1.64811e-05 | 0.00287059 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928369 | ACTTTTCAAGCAATT[A/G]GCAGACTGGTTTTCT | 9169 |
rs775617661 | in-del | -/CT | 3.32132e-05 | 0.00407499 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45927941 | ATTTCTACTAGGGAA[-/CT]CTCTGTTATTTTTTC | 9169 |
rs775655813 | snp | C/T | 1.64781e-05 | 0.00287033 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922109 | TTTTGGCTCCCCTTC[C/T]GTGAATATTTGTATT | 9169 |
rs775681699 | snp | A/G | 0.00015241 | 0.00872822 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948542 | TTTACTTGAACCTAT[A/G]AGAAAAGCAAAATCA | 9169 |
rs775705296 | snp | A/G | 1.69631e-05 | 0.00291226 | missense | SCAF11 | GRCh38.p7 | 12:45931577 | GAAATGAGAGGAAGG[A/G]CTTCTGTTTCAACAT | 9169 |
rs775737508 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45926418 | GATTTTGCCACCGAT[C/T]TTCATTCTGATCTTT | 9169 |
rs775738764 | snp | A/T | | | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964121 | CCTTCCATGTCTTCA[A/T]ACTTCTTATCTCCCA | 9169 |
rs775768723 | in-del | -/AA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45928872 | TACCTAATAATATTT[-/AA]AAAAAAAAAAAAAGT | 9169 |
rs775788208 | snp | A/G | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962655 | TGAACAGTAATATCA[A/G]GCAAAGTTGGAACTG | 9169 |
rs775792642 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924228 | TCTATGTCTCACAGA[A/G]GCACTTCTCCTTTCT | 9169 |
rs775794143 | snp | C/T | 1.65897e-05 | 0.00288003 | missense | SCAF11 | GRCh38.p7 | 12:45927960 | CTGTTATTTTTTCTT[C/T]ATTAACCACTGACTC | 9169 |
rs775861536 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965835 | AAAATTCCCTATTTG[A/G]TTAAATAAGGAGAAA | 9169 |
rs775871667 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971805 | CAGCAGCAGGAACCT[-/A]AAACTCTTAAGAAAA | 9169 |
rs775889521 | snp | C/T | 1.64784e-05 | 0.00287035 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45924878 | GAGATGCAAGGGTAG[C/T]TGAGGATGAATGTTA | 9169 |
rs775907260 | snp | G/T | 1.80543e-05 | 0.00300447 | missense | SCAF11 | GRCh38.p7 | 12:45948523 | TGTTTCTCTCAGCTG[G/T]TTTTTTACTTGAACC | 9169 |
rs775930720 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45954973 | AATTGTCTTAGGTTT[A/G]CCTAGTTTCATTTTA | 9169 |
rs775948871 | snp | C/T | 1.6867e-05 | 0.002904 | missense | SCAF11 | GRCh38.p7 | 12:45924744 | TGCAATTGCTTTCCA[C/T]CTGGTTGTGAAGCAA | 9169 |
rs775977794 | snp | C/T | 3.37764e-05 | 0.00410938 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945363 | AAAAAAACTGTCATT[C/T]TGCTCACTTATTTTC | 9169 |
rs775987120 | in-del | -/TTG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936480 | GGGTTAATAATGTCT[-/TTG]TTTTCTCTTTTCCTT | 9169 |
rs775998979 | snp | C/T | 1.6623e-05 | 0.00288292 | splice-donor-variant | SCAF11 | GRCh38.p7 | 12:45951649 | GAATAAAAAGACTTA[C/T]CTTAACATAACCTTC | 9169 |
rs775999041 | snp | C/T | 3.29549e-05 | 0.00405911 | missense | SCAF11 | GRCh38.p7 | 12:45928659 | TACTGTTACCTGGGG[C/T]ATCACACCCAGAATT | 9169 |
rs776038376 | snp | C/T | 1.66396e-05 | 0.00288436 | missense | SCAF11 | GRCh38.p7 | 12:45924760 | CTGGTTGTGAAGCAA[C/T]GTAGTTGACTTGTTG | 9169 |
rs776041192 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928134 | GGTCTTGCTTTTCCA[A/G]TGGATCACCTCCTTT | 9169 |
rs776043257 | snp | C/T | 1.65061e-05 | 0.00287277 | missense | SCAF11 | GRCh38.p7 | 12:45927026 | CTTGGCTGAGATCTT[C/T]TGTTCTCTCTAGAAG | 9169 |
rs776045906 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938783 | ATCCAATTAAAGTCT[G/T]ACTAATTGATTCCAA | 9169 |
rs776057929 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961617 | TACATTACTGTGAAA[C/T]AATTTATGAAAGGCA | 9169 |
rs776103232 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976991 | ACTATTTGAAGAAAT[A/T]GAATTTGTAGTTAAA | 9169 |
rs776163109 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45927078 | ATTCAGATCTTCTGC[C/T]TTCCCTAGTAGTATC | 9169 |
rs776220921 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989032 | CATGAACTTTTTCTT[A/G]CATCTTTTAACCAAA | 9169 |
rs776267466 | snp | C/T | 1.71369e-05 | 0.00292714 | missense | SCAF11 | GRCh38.p7 | 12:45948494 | TCAAATGAGTTTTCA[C/T]TTTTCTTGTCTTTTG | 9169 |
rs776285867 | snp | A/G | 1.64768e-05 | 0.00287021 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928648 | TAAAGATGGATTACT[A/G]TTACCTGGGGCATCA | 9169 |
rs776291441 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941255 | CACCTTACTTATCGA[A/G]AAACGAATTTGCCTG | 9169 |
rs776293167 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45958012 | ATCCTCCAACCTCCC[A/C]CCATCAGCTTCCCAA | 9169 |
rs776302541 | snp | C/G | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919757 | CACACTTGTTACTGT[C/G]ACGGAAATAATTCAT | 9169 |
rs776323481 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983219 | TTGAGCTTAATGTAG[C/T]AGCAGAAAGGTGGCA | 9169 |
rs776351212 | snp | C/T | 2.22082e-05 | 0.0033322 | missense, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45964128 | TGTCTTCATACTTCT[C/T]ATCTCCCATATTTAG | 9169 |
rs776358175 | snp | A/G | | | downstream-variant-500B | SCAF11 | GRCh38.p7 | 12:45918694 | CCTGGGCAACAGAGC[A/G]AGACTCCATCTCAAA | 9169 |
rs776427262 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982583 | AGTGGTACACGCCTG[A/T]AATCCTAGCTACTCA | 9169 |
rs776453624 | snp | A/G | 1.64806e-05 | 0.00287054 | missense | SCAF11 | GRCh38.p7 | 12:45927509 | GATGGTTCAACTTCA[A/G]ATTCATTTTGGTCAC | 9169 |
rs776458517 | snp | A/T | 0.000323958 | 0.012723 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961867 | CTTCACCTGTTAAAG[A/T]AAAACAGCCATATGT | 9169 |
rs776488327 | snp | C/T | 2.90896e-05 | 0.00381366 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934162 | AGCATAAATTAAAAG[C/T]AGAAAATACTAACCA | 9169 |
rs776492161 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956809 | ATTCTGACATTTAAA[A/C]CTAGGCACAAAGAAA | 9169 |
rs776518842 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45968688 | GCTCACACCTGTAAT[C/T]CCAGCACTTTGGGAG | 9169 |
rs776540469 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946052 | CTGGCTATTGAGCCA[C/T]GCAGACTAGAGGTAA | 9169 |
rs776542391 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959997 | AGCAATTTGAAAAAT[A/G]TTACATGCGGGAAAG | 9169 |
rs776568927 | snp | C/T | 2.42562e-05 | 0.00348246 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934332 | CAAATAAATAACAGG[C/T]AAATAATAGTTATAC | 9169 |
rs776574714 | snp | C/T | 1.64838e-05 | 0.00287083 | missense | SCAF11 | GRCh38.p7 | 12:45928184 | ATCTCACTTTCCAAA[C/T]ACAAAACATTAGCCT | 9169 |
rs776575971 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981885 | GTGCACACCAATTAA[A/G]AGAGATTATCAAACT | 9169 |
rs776581315 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45924012 | CTTGCCACCACACCC[A/G]GCTAATTTTTGTATT | 9169 |
rs776595648 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45960802 | CGCTTTGAAAACCCC[A/G]ATTATGTAATATGCA | 9169 |
rs776604250 | in-del | -/ATATGTTTTAAGAAATAGT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45928894 | AAAAAAAAGTAAAAA[-/ATATGTTTTAAGAAATAGT]AATTTGGCTTTAGCT | 9169 |
rs776615387 | snp | C/T | 8.25035e-05 | 0.00642222 | missense | SCAF11 | GRCh38.p7 | 12:45926414 | TTTCGATTTTGCCAC[C/T]GATTTTCATTCTGAT | 9169 |
rs776617124 | snp | A/G | 0.000115602 | 0.00760182 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927639 | TAGGATGTTCGGTCA[A/G]CGATTCATTCTTTTC | 9169 |
rs776625512 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45977752 | CAAATTATACTGCCA[A/C]AAGATGAGCTTGGGA | 9169 |
rs776647107 | snp | A/G | 1.72513e-05 | 0.0029369 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961689 | AAAATACATTAATGT[A/G]TCAGACTTACCTCTG | 9169 |
rs776704476 | snp | A/G | 1.65304e-05 | 0.00287488 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926545 | ATTTCCTGAATTTTC[A/G]TTTCTATTTTCTTCC | 9169 |
rs776752075 | snp | C/T | | | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45962461 | ATGTGTGTATACATT[C/T]GTATTATGAATAGGT | 9169 |
rs776779806 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939805 | TAGATAAAGAGACAG[A/G]CAACAGTTTCTCAAG | 9169 |
rs776826303 | snp | C/T | 2.35059e-05 | 0.00342818 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925114 | AAAAAAATCATGTTA[C/T]AAATCTCTTTAGACA | 9169 |
rs776847457 | snp | A/G | 1.64776e-05 | 0.00287028 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926218 | GCCTCGTCGTGAGTA[A/G]TAGTTTTGTACATCT | 9169 |
rs776886176 | in-del | -/AGAG | 0.000121521 | 0.00779397 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956196 | TAGATAGCTCCTCTT[-/AGAG]AGAGAGAAACAAGTG | 9169 |
rs776924112 | snp | A/C | 3.34119e-05 | 0.00408715 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928852 | TGCATATCCCTTGCA[A/C]GAAGTACCTAATAAT | 9169 |
rs776926221 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45974801 | CCTTCTATGAATTAC[A/G]AATGTTCTTTATGGC | 9169 |
rs776975564 | snp | C/T | 1.64773e-05 | 0.00287026 | synonymous-codon, intron-variant | SCAF11 | GRCh38.p7 | 12:45922948 | TGCCTTGTCTGTCTT[C/T]GAGCTATCTGCGCTG | 9169 |
rs776991680 | snp | C/T | 1.64988e-05 | 0.00287213 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922068 | CTATGTTTTTTTCAG[C/T]AGACACAGGTTCTTC | 9169 |
rs777005257 | snp | A/T | 1.65102e-05 | 0.00287312 | missense | SCAF11 | GRCh38.p7 | 12:45926976 | GTTCTCTGCTCTGGG[A/T]CCTGGATTTTTCTCC | 9169 |
rs777055898 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966907 | AATATTAAGGTTGGA[C/G]TTAACTCAATGTGAT | 9169 |
rs777084899 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919691 | AGTTCGAATTCTAAT[C/T]AAGTAGCTATTAATG | 9169 |
rs777092274 | snp | A/G | 1.66112e-05 | 0.00288189 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927936 | CAGTAATTTCTACTA[A/G]GGAACTCTCTGTTAT | 9169 |
rs777101240 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990939 | GTGGACTTTGGCCTC[C/T]GCCCTCCTTTGGCAG | 9169 |
rs777102328 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45967955 | TGAATATCCAGTGAC[A/G]GGAACACAGTAATAC | 9169 |
rs777120292 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45973672 | TCAGAAACCATGCAA[A/G]TCAGAAGAAAGGGGA | 9169 |
rs777139006 | in-del | -/TTAGGGGA | 1.6522e-05 | 0.00287414 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45927996 | TCTCAGATAAGTCAC[-/TTAGGGGA]CAAGATACAGGTTGG | 9169 |
rs777155932 | snp | A/C/T | 5.10437e-05 | 0.0050517 | intron-variant | SCAF11 | GRCh38.p7 | 12:45923197 | TGAATTACTTGTACT[A/C/T]GATAGAAGTCTTTTA | 9169 |
rs777158230 | in-del | -/GTAAAGGTG | 1.64827e-05 | 0.00287073 | cds-indel | SCAF11 | GRCh38.p7 | 12:45928545 | GAAGTTTCTTTTTCA[-/GTAAAGGTG]GTTTTCTTCCTCTTC | 9169 |
rs777175372 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45932372 | AGGTAAGATTCTGGA[A/G]TAGGAGAAGCATGGG | 9169 |
rs777177538 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45986180 | CCAGTTTTCCATTTA[C/T]AGCCAATACTCTTCC | 9169 |
rs777219501 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936198 | CCAGGCTGGAGTGCA[C/G]TGCCACAATCTCGGC | 9169 |
rs777257341 | in-del | -/ATATATAGAT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45972922 | TAGATATATATATAG[-/ATATATAGAT]ATATATAGATATATA | 9169 |
rs777261081 | snp | A/C | 1.65012e-05 | 0.00287234 | missense | SCAF11 | GRCh38.p7 | 12:45928022 | GATACAGGTTGGTAC[A/C]CTTTGCTTTCAGATG | 9169 |
rs777285357 | snp | C/T | 3.29647e-05 | 0.00405971 | missense | SCAF11 | GRCh38.p7 | 12:45928092 | ATACATCTGTCTTTA[C/T]CTCTGATTGTGAAAG | 9169 |
rs777317842 | snp | A/C | 1.68943e-05 | 0.00290635 | missense | SCAF11 | GRCh38.p7 | 12:45948468 | AATTTTCATGACAGG[A/C]GACCTGTTTCTCAAA | 9169 |
rs777362758 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934812 | ACCTTATGCAAACTT[A/G]AAGTATCTTGTAACA | 9169 |
rs777394821 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934655 | TTTTACACAATTTTC[C/T]CAAATGCTGATTTCA | 9169 |
rs777397726 | snp | G/T | 1.64972e-05 | 0.00287199 | missense | SCAF11 | GRCh38.p7 | 12:45926955 | GCCCATCTCTATCAC[G/T]TTCTCGTTCTCTGCT | 9169 |
rs777469576 | snp | A/G | 0.000122108 | 0.00781274 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956231 | TAAGACAAGTGCTTA[A/G]AGACTAAATCTCAAT | 9169 |
rs777475050 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988026 | CAAGAGAATGATACT[A/G]GATATTTTAACTCTG | 9169 |
rs777504322 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982989 | AATGTGAGAAATAGG[C/T]AAAGAGTTTCTAAGA | 9169 |
rs777624200 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940701 | TTTGGAATACTTCAA[C/T]CAGGTTAGTTTATCT | 9169 |
rs777636903 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976173 | ACATACATGGTGGTA[A/T]GACCTCTATTTCACT | 9169 |
rs777659451 | snp | A/G | 1.67801e-05 | 0.00289651 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951611 | AAACAGCTTCAATTA[A/G]TTTTTATATAATTCA | 9169 |
rs777670825 | in-del | -/CTTA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929975 | TTATTCACCAGACTC[-/CTTA]CTGATAACAGTGAAT | 9169 |
rs777676668 | snp | A/G | 0.000164742 | 0.00907435 | missense | SCAF11 | GRCh38.p7 | 12:45924939 | GCATGAACACCCACT[A/G]GATATGGGAAGATAT | 9169 |
rs777676914 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955795 | CTGACTTTCATTTCA[A/G]TAATTTTTAAAGTAT | 9169 |
rs777738847 | in-del | -/TCA | 1.64798e-05 | 0.00287047 | cds-indel | SCAF11 | GRCh38.p7 | 12:45926696 | GCATCTAGATGGATG[-/TCA]TTTTTTTCTTTTCTT | 9169 |
rs777819085 | in-del | -/AT | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951076 | AAGCAAAAAATTAAC[-/AT]AAATACAAATCATAA | 9169 |
rs777837621 | snp | C/T | 1.6476e-05 | 0.00287014 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928717 | ACTGGCTGTTTCAGC[C/T]CTTGTGTTACGTGTA | 9169 |
rs777856004 | snp | C/T | 1.64879e-05 | 0.00287118 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927622 | AGGCAACTCTGTAGA[C/T]CTAGGATGTTCGGTC | 9169 |
rs777868744 | snp | C/T | 1.70656e-05 | 0.00292104 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934535 | AAAAGGACTTGGTTA[C/T]CTTGTATTAATTTTT | 9169 |
rs777872043 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939646 | GAGGTTGCAGTGAGC[C/T]GAGATCGTGCCATTG | 9169 |
rs777935706 | snp | C/G | 1.6473e-05 | 0.00286988 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923015 | TTTACAGCAGCATTA[C/G]AGGCTTTGCTGTGAC | 9169 |
rs777947479 | snp | A/T | 1.64754e-05 | 0.00287009 | missense | SCAF11 | GRCh38.p7 | 12:45927365 | GTTTTATCTATGGTA[A/T]CTTTTGGGCTTTCAG | 9169 |
rs777955104 | snp | A/C | 1.64814e-05 | 0.00287061 | missense | SCAF11 | GRCh38.p7 | 12:45928348 | TTCTTCTATTTGCTC[A/C]TTGCAACTTTTCAAG | 9169 |
rs777955142 | snp | A/G | 1.66078e-05 | 0.00288161 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45945280 | GTCACAAACTTTTGC[A/G]CTTAATAGATCTTCT | 9169 |
rs777956069 | snp | C/T | 9.88435e-05 | 0.00702937 | missense | SCAF11 | GRCh38.p7 | 12:45926753 | TCATTCTTTCTGTAC[C/T]GATCATTTCCTCGTG | 9169 |
rs777971280 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980366 | CCAATTATTTATGGA[C/T]ATGTTTAGCAACCAT | 9169 |
rs777971574 | snp | C/T | 1.64844e-05 | 0.00287087 | missense | SCAF11 | GRCh38.p7 | 12:45928443 | GTTGGTGCTCTTTTT[C/T]TAACACAGGTGATGT | 9169 |
rs778017525 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982058 | ACTATATTTTAAACC[-/T]TTTTAAAGAGTCTAA | 9169 |
rs778035871 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975403 | CATTAAAAATCTTTT[A/G]TTTAGTATAGCCACT | 9169 |
rs778060833 | snp | C/T | 1.64868e-05 | 0.00287109 | missense | SCAF11 | GRCh38.p7 | 12:45927285 | TTTCTTGTGGAGTGT[C/T]TTTGTTGGGTGACCA | 9169 |
rs778078307 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966860 | CATACCATACTATCT[C/T]CTTCATTATCCTAAA | 9169 |
rs778119654 | snp | A/C | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45921984 | TATGATTTTCAGTTA[A/C]TGGTACATGTTGAAA | 9169 |
rs778130382 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969500 | GTTAATACTACAAAC[-/T]TTAGAATCCAACAGG | 9169 |
rs778131047 | snp | A/G | 4.94621e-05 | 0.00497279 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923114 | GCAGGCAAAACTGGT[A/G]TACTCATGTTATTAC | 9169 |
rs778133599 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980374 | TTATGGATATGTTTA[C/G]CAACCATAGCACATG | 9169 |
rs778208096 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929706 | TAAAACTGACTAACA[C/G]ATAAAACTGTGTTTC | 9169 |
rs778222898 | snp | C/T | | | missense | SCAF11 | GRCh38.p7 | 12:45924925 | TGTTCATCAAAGGAG[C/T]ATGAACACCCACTGG | 9169 |
rs778242691 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984695 | GCTCTTCGCACTTCC[-/T]TTTTTTTTTTTTTTT | 9169 |
rs778277747 | snp | A/G | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993230 | AAAAGCACAAATGAT[A/G]TGCATCATAAAACAG | 9169 |
rs778289522 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946908 | TACCTTGAAATCATA[C/T]ACAAAGTTTTATGTC | 9169 |
rs778290365 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945060 | TAAGAGGAGCAAGAA[C/G]GAAAAAAGGGGCAGA | 9169 |
rs778330144 | snp | C/T | 1.65842e-05 | 0.00287955 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961801 | GACATATTGGGCATC[C/T]GTCAGCCTCACTGTA | 9169 |
rs778353663 | snp | C/T | 1.65616e-05 | 0.00287759 | intron-variant, upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45961654 | ACTCTTTAGGTGAAA[C/T]GAAATCATGCTAGGA | 9169 |
rs778363779 | snp | A/G | 8.29882e-05 | 0.00644106 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961816 | TGTCAGCCTCACTGT[A/G]CAACAGACCAGTGGA | 9169 |
rs778398380 | snp | A/G | 1.64757e-05 | 0.00287012 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926332 | TTCACTTTTTCGCTT[A/G]TAGGATTGCTGTTCC | 9169 |
rs778419949 | snp | C/T | 1.92302e-05 | 0.00310076 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931622 | CCAATTCTGAAAACA[C/T]AATAAAGACATTTTT | 9169 |
rs778482393 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959891 | CTTTAAAGGTTAATT[A/G]CCTTTGTTTAAACAC | 9169 |
rs778523900 | snp | C/T | 1.65913e-05 | 0.00288017 | missense | SCAF11 | GRCh38.p7 | 12:45927879 | ATTCTAACTTGGGGC[C/T]CTCTATAAGCTCCTC | 9169 |
rs778525564 | snp | C/T | 3.42524e-05 | 0.00413824 | missense | SCAF11 | GRCh38.p7 | 12:45926144 | AAGAATACATTACCC[C/T]GTCCAGATGTTTCCT | 9169 |
rs778529010 | snp | C/T | 9.29152e-05 | 0.00681535 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931472 | AACTAATAATAATAA[C/T]TTTTAAAATAGAAAA | 9169 |
rs778539738 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982681 | CTGCACTCCAGCCTG[A/G]GTGACAGAATGAGAC | 9169 |
rs778588664 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925643 | CAAGAAACTGACTAG[C/T]TAAAAAAAAAAATCA | 9169 |
rs778630341 | snp | C/T | 1.64855e-05 | 0.00287097 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45926932 | TCTCCTTTCTCTCTC[C/T]CTCCTCTGCCCATCT | 9169 |
rs778653031 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987096 | CTGGGTGTGGTGGTT[C/T]ATTCCTGTAATCCCA | 9169 |
rs778687684 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934052 | GCCCAAAAAAAAACT[-/A]AAGCAAAACAACCAG | 9169 |
rs778695189 | snp | C/T | 1.67787e-05 | 0.00289639 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922031 | TCCTGATAATGTCCT[C/T]GACAGCGTTCCCCAT | 9169 |
rs778710460 | in-del | -/G | | | | | GRCh38.p7 | 12:45938740 | TATAATAAAGGCTCT[-/G]GAGCTTAGAACCCAG | 9169 |
rs778765541 | snp | A/C | 1.65187e-05 | 0.00287386 | missense | SCAF11 | GRCh38.p7 | 12:45924838 | TGGTAGGAGTGGCTA[A/C]CTGCATGAGGGGCAC | 9169 |
rs778789771 | snp | C/T | 1.6495e-05 | 0.0028718 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927052 | AGAAGTTTCTCTTCT[C/T]GGGGACAGTGATTCA | 9169 |
rs778793385 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941186 | ATGAGTAGATCTTAT[C/T]TGTACATGAAATGCA | 9169 |
rs778794511 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987788 | GAAAAGAAGTTACAT[A/G]ACCTGACATTTTATC | 9169 |
rs778904942 | snp | A/G | 1.7939e-05 | 0.00299486 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924715 | GATTAAACTTGAGTT[A/G]CTAAAAACATACCTG | 9169 |
rs778918076 | snp | A/G | 1.66913e-05 | 0.00288883 | intron-variant | SCAF11 | GRCh38.p7 | 12:45945332 | TAAACATCAATAAAG[A/G]CAGGAAAGAATTAAG | 9169 |
rs778991619 | in-del | -/TAAAGT | 1.73309e-05 | 0.00294366 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948420 | TTTGCATTCCACTTC[-/TAAAGT]TAATCACTAACCTTA | 9169 |
rs779000398 | snp | C/T | 1.72184e-05 | 0.00293409 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922613 | TGTATAATTTATTAT[C/T]TGCCAGTCATACTGC | 9169 |
rs779034782 | snp | A/G | 5.57243e-05 | 0.00527817 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964238 | TGCCTTCTCCCAATA[A/G]TATCAATTAAAAAAA | 9169 |
rs779041279 | snp | A/T | | | missense | SCAF11 | GRCh38.p7 | 12:45928801 | TGATGTACCAGAAGT[A/T]TGCTTCTTTTCTTCC | 9169 |
rs779042302 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938470 | CTCCAGCCTGGGTGA[C/G]AAGAGCGAGACTGCA | 9169 |
rs779046445 | in-del | -/T | 0.000745838 | 0.0192967 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928869 | AAGTACCTAATAATA[-/T]TTAAAAAAAAAAAAA | 9169 |
rs779066225 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965681 | TGAAATGTCCAAATA[C/T]GCATTTATATCTACG | 9169 |
rs779096463 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942868 | TTTGCGTTTGTCTAC[A/G]AGAAGATCCCATTGA | 9169 |
rs779108942 | snp | A/G | 4.94376e-05 | 0.00497156 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923103 | CTGCTGTCGGAGCAG[A/G]CAAAACTGGTGTACT | 9169 |
rs779121313 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45978057 | ATTTACAACGCAGTA[C/T]TTTATTTAAGAAAAT | 9169 |
rs779141615 | snp | G/T | 8.46145e-05 | 0.00650385 | intron-variant | SCAF11 | GRCh38.p7 | 12:45934515 | AGTTTCCTGTACAAA[G/T]ACATAAAAGGACTTG | 9169 |
rs779163541 | snp | C/T | 1.65206e-05 | 0.00287403 | missense | SCAF11 | GRCh38.p7 | 12:45926622 | GCCCAGAGTTTATTT[C/T]TTCTGTTATCCAATT | 9169 |
rs779197333 | snp | A/T | 4.9445e-05 | 0.00497193 | missense | SCAF11 | GRCh38.p7 | 12:45928340 | TTCTCACTTTCTTCT[A/T]TTTGCTCATTGCAAC | 9169 |
rs779202929 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45981197 | TTCTAACTGGCCAGT[C/T]TTCTGCTATGTTCAC | 9169 |
rs779222069 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951756 | AACAAATTATATCTT[C/T]ACAAATGTTTCTTTA | 9169 |
rs779227215 | snp | C/T | 1.64887e-05 | 0.00287125 | missense | SCAF11 | GRCh38.p7 | 12:45928259 | ACTAGCACAGGAAGA[C/T]CTTGAGCACAAGACT | 9169 |
rs779231426 | snp | C/T | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45992629 | ACTCCTGGTGCAACA[C/T]GCTTCTGTGTATGTT | 9169 |
rs779259650 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980270 | TTAATGATTCAAATG[A/G]CTGCAAAAATGTTAA | 9169 |
rs779272319 | in-del | -/CAACTCAA | 1.6669e-05 | 0.00288691 | frameshift-variant | SCAF11 | GRCh38.p7 | 12:45925057 | TTGCTGGTTTGTTTG[-/CAACTCAA]GTCTTTTAGGCTAGA | 9169 |
rs779284927 | snp | A/G | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45991084 | GTCCGCATGTTTGCG[A/G]TGGATTGAGTGTTCA | 9169 |
rs779285230 | snp | C/T | 4.95217e-05 | 0.00497578 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927268 | AGACTGGGGCCGCTT[C/T]TTTTCTTGTGGAGTG | 9169 |
rs779296899 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945863 | TTATTCTTATTATTA[-/T]TTTTTTTTACTAGAC | 9169 |
rs779299069 | in-del | -/GA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953437 | TAATGCCAACACTTT[-/GA]GAGGCCAAGGCAGGA | 9169 |
rs779337189 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45942020 | CTCAATGAACAGTAA[A/C]TGTATTTTCTCATCC | 9169 |
rs779375232 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929468 | CGGCCATGATCTGGG[A/T]TTATCTAAGCAAAAG | 9169 |
rs779393467 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945415 | ATGAAATCTATCATG[A/C]ACTGATTTTGGTAAC | 9169 |
rs779447050 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959965 | AGCAGCATAAAGATA[A/C]GTACTTTCTTTTGAA | 9169 |
rs779556934 | snp | C/T | 1.64754e-05 | 0.00287009 | missense | SCAF11 | GRCh38.p7 | 12:45924973 | TAGGCTGGTGTTGTG[C/T]ATTCATTTGTTGCTG | 9169 |
rs779557779 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45923574 | AAAAAAGGCTTGCAG[G/T]AAGTTGACAGGAGAA | 9169 |
rs779560873 | in-del | -/CTTA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929144 | TGTAACTGCTACTTG[-/CTTA]ATTTTTTTTTTTTTT | 9169 |
rs779566035 | snp | C/G | 1.73126e-05 | 0.00294211 | missense | SCAF11 | GRCh38.p7 | 12:45925071 | TGGTCTTTTAGGCTA[C/G]AATCTATCAAAAGAA | 9169 |
rs779578727 | snp | C/T | 1.66056e-05 | 0.00288141 | missense | SCAF11 | GRCh38.p7 | 12:45951721 | CAATAGGACATGAAG[C/T]CAGTGTCTGAAAAGT | 9169 |
rs779585223 | snp | A/G | 1.96419e-05 | 0.00313378 | intron-variant | SCAF11 | GRCh38.p7 | 12:45925090 | CTATCAAAAGAAAAA[A/G]AGCTTGTGAAAAAAA | 9169 |
rs779606821 | snp | A/G | 1.65581e-05 | 0.00287728 | missense | SCAF11 | GRCh38.p7 | 12:45927756 | TCCCAAAAGTATCAC[A/G]TGTTGCAATTATTTC | 9169 |
rs779620226 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45971859 | AAATAAAAAAACTCT[G/T]GGCCAATCTTGTTGA | 9169 |
rs779625489 | snp | A/G | 0.000121529 | 0.00779421 | intron-variant | SCAF11 | GRCh38.p7 | 12:45956204 | TCCTCTTAGAGAGAG[A/G]GAAACAAGTGTTAAG | 9169 |
rs779666756 | snp | A/C | 1.64901e-05 | 0.00287137 | missense | SCAF11 | GRCh38.p7 | 12:45928807 | ACCAGAAGTTTGCTT[A/C]TTTTCTTCCCCTTCT | 9169 |
rs779666848 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963610 | TCAGAAAGAAAATAA[A/G]TGAAGAGGAAATAAA | 9169 |
rs779714204 | snp | C/T | 1.93444e-05 | 0.00310996 | intron-variant | SCAF11 | GRCh38.p7 | 12:45928909 | ATATGTTTTAAGAAA[C/T]AGTAATTTGGCTTTA | 9169 |
rs779717763 | in-del | -/TT | 1.6654e-05 | 0.00288561 | intron-variant | SCAF11 | GRCh38.p7 | 12:45951739 | GTGTCTGAAAAGTGA[-/TT]AACAAATTATATCTT | 9169 |
rs779719367 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45936833 | AGCAGAAGTGGAAAA[A/G]GGTGGGAATTCTGAG | 9169 |
rs779751016 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45974096 | TCACACAAAATTTTT[C/G]GTTTCCTAGTATATA | 9169 |
rs779806814 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45922289 | AACCCCAAAGAGATA[A/G]CCAGACTTATTTTCA | 9169 |
rs779827399 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45959056 | TGAATCATATTTCAG[C/T]GAACCTTGGGTACAA | 9169 |
rs779849728 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938316 | CCAACATGGTGAAAC[C/G]CTGCTCTACTAAAAA | 9169 |
rs779858245 | snp | A/C | 1.68783e-05 | 0.00290498 | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45922018 | CACTTTGCAGATATC[A/C]TGATAATGTCCTTGA | 9169 |
rs779887204 | snp | A/G | 3.32375e-05 | 0.00407647 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45945301 | TAGATCTTCTCTTAC[A/G]ATGGCTTTTCTTCTG | 9169 |
rs779951927 | snp | A/C | 1.65803e-05 | 0.00287922 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927859 | TATAATTTCACCCTC[A/C]GAAGATTCTAACTTG | 9169 |
rs779998448 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45951836 | CTCTATCTTCGAAAG[A/C]AAAAAATATTTTTAT | 9169 |
rs780050628 | snp | C/T | 1.648e-05 | 0.0028705 | missense | SCAF11 | GRCh38.p7 | 12:45927465 | GTGTCACAGAATTTT[C/T]ATTCATTTGTTTAAG | 9169 |
rs780076616 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45976607 | TGGAATACTAAAAAA[A/G]TGTTCAAATAACCCA | 9169 |
rs780160446 | snp | A/T | 3.29875e-05 | 0.00406112 | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45923121 | AAACTGGTGTACTCA[A/T]GTTATTACTTACATG | 9169 |
rs780224708 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987303 | CATGGCCCACATGCA[A/T]GGATATAAGTAACTT | 9169 |
rs780251643 | snp | C/T | | | upstream-variant-2KB, intron-variant | SCAF11 | GRCh38.p7 | 12:45990938 | CGTGGACTTTGGCCT[C/T]TGCCCTCCTTTGGCA | 9169 |
rs780252729 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45965152 | TACAAATTCTATGAA[C/G]AAGAGTGACAAGATA | 9169 |
rs780255887 | snp | A/T | 5.65547e-05 | 0.00531734 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964090 | AACAAACAAACTTTA[A/T]AAAAATGAAAAGTTA | 9169 |
rs780265581 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45989720 | GAATTTAAAACACTG[C/G]GGGTGGATGAGTAGT | 9169 |
rs780301281 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45941674 | AGTAACTGGCAACTC[C/T]TATTTTACCAGTTCC | 9169 |
rs780318996 | snp | A/G | 1.64787e-05 | 0.00287038 | missense | SCAF11 | GRCh38.p7 | 12:45927587 | CTAAAATGCTTCTGA[A/G]TCTGTTCAATGTGTG | 9169 |
rs780322702 | snp | C/G | 1.86458e-05 | 0.00305328 | missense | SCAF11 | GRCh38.p7 | 12:45934250 | GGAGAAAAAATTTCT[C/G]AAGCACTGATTTGTA | 9169 |
rs780327905 | snp | A/G | 1.70641e-05 | 0.00292092 | intron-variant | SCAF11 | GRCh38.p7 | 12:45922601 | ATGAGAAGAAAATGT[A/G]TAATTTATTATTTGC | 9169 |
rs780334214 | snp | C/T | 9.88582e-05 | 0.00702989 | missense | SCAF11 | GRCh38.p7 | 12:45928713 | ACTGACTGGCTGTTT[C/T]AGCTCTTGTGTTACG | 9169 |
rs780347537 | snp | C/T | 1.74482e-05 | 0.00295361 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933253 | AGATAAATTTTAGAC[C/T]TTCATCAGAATCTCA | 9169 |
rs780398873 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949375 | AAAATCTCTCAATAA[G/T]AATTTTAAAATATTA | 9169 |
rs780612038 | snp | C/T | | | missense, intron-variant | SCAF11 | GRCh38.p7 | 12:45922148 | TAGGCTTTAACCAGA[C/T]TTGCCACTTTAGTAG | 9169 |
rs780641480 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985531 | AGATGGACCCAGCTA[C/T]AGATACTTAGCAACT | 9169 |
rs780648007 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45934581 | AACCAGCATCGATAC[C/T]AGCACATTGGCAAGG | 9169 |
rs780674111 | snp | C/G | 3.29707e-05 | 0.00406008 | missense | SCAF11 | GRCh38.p7 | 12:45927164 | GGGGACTGAGAACGG[C/G]ATTTTTTCCGGCCTC | 9169 |
rs780680935 | snp | A/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969164 | ACTGTAGAGCACAAC[A/T]GTTAAAAACCTGTTT | 9169 |
rs780699433 | snp | C/T | 3.29919e-05 | 0.00406138 | missense | SCAF11 | GRCh38.p7 | 12:45927077 | GATTCAGATCTTCTG[C/T]TTTCCCTAGTAGTAT | 9169 |
rs780704372 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919553 | TGTTTCTGATTAAGT[C/T]TGTGCCCATGCAAAA | 9169 |
rs780714781 | snp | C/T | 1.64833e-05 | 0.00287078 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928327 | ATTTGCAGTATGCTT[C/T]TCACTTTCTTCTATT | 9169 |
rs780735397 | snp | A/T | 3.295e-05 | 0.00405881 | missense | SCAF11 | GRCh38.p7 | 12:45928722 | CTGTTTCAGCTCTTG[A/T]GTTACGTGTAGACCT | 9169 |
rs780761829 | snp | G/T | 0.0167329 | 0.0899248 | missense | SCAF11 | GRCh38.p7 | 12:45924966 | ATATTCATAGGCTGG[G/T]GTTGTGCATTCATTT | 9169 |
rs780794291 | in-del | -/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45929148 | CTGCTACTTGCTTAA[-/T]TTTTTTTTTTTTTTG | 9169 |
rs780798244 | snp | C/T | 1.64906e-05 | 0.00287142 | missense | SCAF11 | GRCh38.p7 | 12:45928230 | CGAGTTTTTTAACTT[C/T]CCCTTCCTCACCAAC | 9169 |
rs780798435 | snp | A/C | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45985418 | CATACTTCTTAGATA[A/C]CCCATACTGAAGATT | 9169 |
rs780807854 | snp | A/C | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45920915 | CGAATTGGCACAAAT[A/C]ATTTATCGTCTGCAA | 9169 |
rs780820299 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938107 | ACCATCCCCCTCATA[C/G]TGTTTTACTTTCTAT | 9169 |
rs780884255 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940243 | CCTTTAACCTGAAGG[-/A]AAAAAAAAATCACAG | 9169 |
rs780886315 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45987432 | CTTACACTGAAGGCA[C/T]TGTTCAGGTGTTTAG | 9169 |
rs780964782 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970946 | CACACTATGCTCTAC[A/G]ATGATCAAAAACCTA | 9169 |
rs780992068 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45966941 | ATGTCATTTGAAAGT[G/T]AACACAGTATTTTAA | 9169 |
rs781001492 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45949996 | ATATGACAAAGAAGA[C/T]TGTGAAAGGACAGAG | 9169 |
rs781017518 | snp | A/G | 0.000487211 | 0.0156003 | upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45991993 | ACGCCTGCCCGGGAT[A/G]AGTTTCCTCCCCACT | 9169 |
rs781018256 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45984137 | GAACCCAGATTAAGA[C/T]TCTTTTTACCTTAAT | 9169 |
rs781089686 | snp | A/G | 1.64822e-05 | 0.00287068 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45928795 | GGTATTTGATGTACC[A/G]GAAGTTTGCTTCTTT | 9169 |
rs781265327 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45970408 | GATATAAATGGCCAC[A/G]AGGAAATATCACACT | 9169 |
rs781274012 | snp | A/G | | | intron-variant, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45975043 | CTACGTGCACTGTCA[A/G]TAAGTAAGTACTATG | 9169 |
rs781285301 | snp | A/G | 3.30344e-05 | 0.004064 | missense | SCAF11 | GRCh38.p7 | 12:45926627 | GAGTTTATTTTTTCT[A/G]TTATCCAATTGGGAC | 9169 |
rs781286268 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45925998 | GTATATATATTTATA[C/T]AATGCTAAGTGACTT | 9169 |
rs781336590 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45940930 | CCACCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC | 9169 |
rs781352105 | snp | A/G | 1.84021e-05 | 0.00303327 | intron-variant | SCAF11 | GRCh38.p7 | 12:45924697 | GTTTACAATGGCTAT[A/G]TTGATTAAACTTGAG | 9169 |
rs781356313 | snp | C/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45939584 | ATGCCTGTAATCCCA[C/G]CTACTTGGGAGGCTG | 9169 |
rs781357768 | in-del | -/AATA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45955627 | AAAGAAATTTTAACT[-/AATA]CTTACTCTATTTTTA | 9169 |
rs781373320 | snp | A/C | 1.72603e-05 | 0.00293766 | intron-variant | SCAF11 | GRCh38.p7 | 12:45948422 | TGCATTCCACTTCTA[A/C]AGTTAATCACTAACC | 9169 |
rs781382536 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45969059 | ATGTGAGAAACTAAA[C/T]TTTAAATTTTTGTGA | 9169 |
rs781385826 | snp | A/T | 1.64757e-05 | 0.00287012 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927388 | GCTTTCAGATGGTTG[A/T]GAAACAGTTTCAACC | 9169 |
rs781400261 | snp | A/C | 1.64798e-05 | 0.00287047 | synonymous-codon | SCAF11 | GRCh38.p7 | 12:45927454 | TTCAGAACAGTGTGT[A/C]ACAGAATTTTCATTC | 9169 |
rs781429500 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982562 | ATACAAAAATTAGCC[A/G]GGTGTAGTGGTACAC | 9169 |
rs781449687 | snp | C/T | 3.03311e-05 | 0.00389418 | intron-variant | SCAF11 | GRCh38.p7 | 12:45964074 | CAACTGTTTTGCTTT[C/T]AACAAACAAACTTTA | 9169 |
rs781455359 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45956037 | CACACCCTACTATTC[C/T]GAAGCATTATAAATT | 9169 |
rs781465132 | snp | C/T | 1.64806e-05 | 0.00287054 | missense | SCAF11 | GRCh38.p7 | 12:45928572 | TTCTTCCTCTTCTTA[C/T]AGACTTCCGTTTTGG | 9169 |
rs781492143 | snp | A/T | 0.000148286 | 0.00860936 | missense | SCAF11 | GRCh38.p7 | 12:45926352 | ATTGCTGTTCCACAA[A/T]CTTGAAAGATTCACT | 9169 |
rs781497795 | snp | A/T | 1.66638e-05 | 0.00288645 | missense, upstream-variant-2KB, utr-variant-5-prime | SCAF11 | GRCh38.p7 | 12:45961831 | ACAACAGACCAGTGG[A/T]AATAGTATTATCTCC | 9169 |
rs781505783 | snp | C/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45988214 | GACAAAAGCAGGTGA[C/T]AGCAGGGCTTGCTAA | 9169 |
rs781567167 | snp | C/T | | | utr-variant-3-prime, intron-variant | SCAF11 | GRCh38.p7 | 12:45919661 | ATACATTCTTAAACA[C/T]TTCAAAATTTTAAAA | 9169 |
rs781717642 | in-del | -/ATG | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983065 | AAGTAAAGAAAAATA[-/ATG]ATAATAAAGTGCAAA | 9169 |
rs781718953 | snp | C/T | 2.46381e-05 | 0.00350977 | intron-variant | SCAF11 | GRCh38.p7 | 12:45931657 | AAATGGTTTAAAAAA[C/T]TAAACCACCAATTTA | 9169 |
rs781721710 | in-del | -/TAC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45953111 | TAGGAAATGTGACCT[-/TAC]TACTATATTAAATTG | 9169 |
rs781748248 | snp | G/T | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946692 | CCAGTGATATGAGTT[G/T]TATCAAGAATTAAAA | 9169 |
rs781761156 | snp | C/T | 3.36865e-05 | 0.00410391 | missense | SCAF11 | GRCh38.p7 | 12:45933228 | TGGCTTCTATAAATT[C/T]TGTACTAAAAGATAA | 9169 |
rs781763627 | snp | C/T | 1.65636e-05 | 0.00287776 | intron-variant | SCAF11 | GRCh38.p7 | 12:45933081 | AGTACTAATGCTATC[C/T]TGTTCATGTTAGCAT | 9169 |
rs796109869 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45979888 | TGCAAACTTAAAATT[-/A]AAAAAAAAAAAAATT | 9169 |
rs796221969 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45963458 | TCAAAGTGCTAAGAG[-/A]AAAAAAAACTATCAT | 9169 |
rs796236801 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45946652 | GGGAGAAAAAAAAAA[-/A]TGCATATCTATGATA | 9169 |
rs796280907 | in-del | -/CA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45983784 | ACACACACACACACA[-/CA]AAGACTGAACTAATT | 9169 |
rs796427665 | in-del | -/CCAAAATACCTGTGTTTGGGAGGAGTGTTCCTCCTC | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45980847 | CTGCTCCACCAGGTT[lengthTooLong]CCAAAATACACTAAT | 9169 |
rs796505793 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45947604 | TTTACAGTGTGGTAT[A/G]AGCACCAATGCTTAT | 9169 |
rs796564742 | in-del | -/A | | | upstream-variant-2KB | SCAF11 | GRCh38.p7 | 12:45993779 | GTAAGACTCCATCTC[-/A]AAAAAAAAAAAAAAG | 9169 |
rs796705188 | snp | A/G | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45982478 | TCAGGAGGCCAAGGC[A/G]GGCAGATCACTTGAG | 9169 |
rs796774857 | in-del | -/A | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45945210 | AAATTAAAAAACAAC[-/A]AAAAAAAAGGTAGAA | 9169 |
rs797003912 | in-del | -/AA | | | intron-variant | SCAF11 | GRCh38.p7 | 12:45938503 | TCAAAAAAACAAACA[-/AA]CAAACAAACAAAAAA | 9169 |