SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13748 | snp | A/G | 0.326195 | 0.238106 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41937416 | AAGATTAGAACCCAC[A/G]TTTGAGATCGATGAA | 7994 |
rs15329 | snp | A/T | 0 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930950 | TGAGTTCATCCCCTG[A/T]GAATCAGAGTGCACA | 7994 |
rs997437 | snp | A/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42037199 | GTAATGCTAAAGTGA[A/T]TTTAGTGCCAAGTAC | 7994 |
rs1050989 | snp | A/C | | | synonymous-codon | KAT6A | GRCh38.p7 | 8:41940971 | AAGTGAGAGGCTGCC[A/C]CGTCGCTACAGTGAG | 7994 |
rs1050991 | snp | C/G | 0.151334 | 0.229706 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41932020 | TGGGTTCATTTTGTT[C/G]TGGGTTTTGGTTTTC | 7994 |
rs1131463 | snp | A/C/T | | | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930754 | GCTCCAGGGATAGGT[A/C/T]aaaaaaaaaaaaaaa | 7994 |
rs1317009 | snp | C/G | 0.0138799 | 0.0821421 | intron-variant | KAT6A | GRCh38.p7 | 8:41964201 | AATTTATAACTCTAG[C/G]TAAAACAATCCTTCT | 7994 |
rs1317010 | snp | C/T | 0.274929 | 0.248754 | intron-variant | KAT6A | GRCh38.p7 | 8:41964384 | TATTcaatagtcccc[C/T]ttatccacccactgg | 7994 |
rs1318481 | snp | G/T | 0.49995 | 0.00499176 | intron-variant | KAT6A | GRCh38.p7 | 8:41940384 | CAAGATGAGCTACTG[G/T]ACTCTGAGTACCCCA | 7994 |
rs1344219 | snp | C/T | 0.271162 | 0.249103 | intron-variant | KAT6A | GRCh38.p7 | 8:41973655 | TGGCAGGAGGTGAGG[C/T]TGGAAAAGTGCAGGG | 7994 |
rs1871991 | snp | C/T | 0.499683 | 0.0125759 | intron-variant | KAT6A | GRCh38.p7 | 8:41966020 | TAAGAGCCTGGGAAC[C/T]AGAAAAGGCTAGCAC | 7994 |
rs1905238 | snp | A/T | 0.32 | 0.24 | intron-variant | KAT6A | GRCh38.p7 | 8:42005796 | CACACACACACACAC[A/T]CACTCACTCTCTTTC | 7994 |
rs2128608 | snp | G/T | 0.255782 | 0.249933 | intron-variant | KAT6A | GRCh38.p7 | 8:42003306 | CAGATCTCTCAAAAA[G/T]ATGTCTTGCCCTGCT | 7994 |
rs2277132 | snp | A/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42037795 | GTTATTTTACAAACA[A/T]CTGTCCTCAATCTTA | 7994 |
rs2355642 | snp | C/T | 0.422473 | 0.180978 | intron-variant | KAT6A | GRCh38.p7 | 8:42012732 | gccacaggaaactaC[C/T]GTACtatattcacac | 7994 |
rs2355643 | snp | C/T | 0.372592 | 0.217879 | intron-variant | KAT6A | GRCh38.p7 | 8:42029956 | ttttctttttttcca[C/T]tggactctttctgga | 7994 |
rs2355644 | snp | A/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42031038 | ATGCAAAAAAAAAAA[A/G]GGGGGGGGGGACAGG | 7994 |
rs2929895 | snp | A/G | 0.403158 | 0.197592 | intron-variant | KAT6A | GRCh38.p7 | 8:41936121 | ACAAAAATTAGCCAG[A/G]CATGGTGGCGTGCAC | 7994 |
rs2929896 | snp | G/T | 0.411578 | 0.190768 | intron-variant | KAT6A | GRCh38.p7 | 8:41940684 | TCTCAAATGTTCACT[G/T]GGAAGATCTTGAGCT | 7994 |
rs2929897 | snp | A/G | 0.419776 | 0.18351 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942375 | TGTCCTGAACTCCTA[A/G]TCTCAAGCAATCCTC | 7994 |
rs2929898 | snp | C/T | 0.424073 | 0.17944 | intron-variant | KAT6A | GRCh38.p7 | 8:41946493 | TTAAATATATATATa[C/T]acacacacacacaca | 7994 |
rs2939983 | snp | C/T | 0 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41929776 | TCTAGCGTGTGTGAA[C/T]AGAGCTCCAGATGCC | 7994 |
rs2980901 | snp | C/G | 0.0448448 | 0.142868 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933348 | GCAGCAGAGCAGCGT[C/G]CAGCCTGCTGCCAAC | 7994 |
rs2980902 | snp | C/T | 0.489796 | 0.070696 | intron-variant | KAT6A | GRCh38.p7 | 8:41946529 | ACACACACACACACA[C/T]ACACACACACACAGA | 7994 |
rs3041258 | in-del | -/CT/TC | | | intron-variant | KAT6A | GRCh38.p7 | 8:42005797 | cacacacacacacac[-/CT/TC]ACTCACTCTCTTTCT | 7994 |
rs3739365 | snp | A/G | 0.212512 | 0.247173 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933765 | GGGGTGAGACTGAAC[A/G]GAGGAGATAGGGCTA | 7994 |
rs3739366 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | KAT6A | GRCh38.p7 | 8:42037142 | GGCCTCACTACTAGT[C/G]AAATTTAATTAGTTT | 7994 |
rs3780018 | snp | A/G | 0.374 | 0.217081 | intron-variant | KAT6A | GRCh38.p7 | 8:41944670 | AAACGTATTACATTA[A/G]GAAAAGTAAATACAA | 7994 |
rs3780019 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41985400 | TCTTAAGACTCCTTT[A/G]CAGCTAGGCTCTAAG | 7994 |
rs3824275 | snp | C/T | 0.213638 | 0.247347 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41940899 | TGACCGAGGGCTTTC[C/T]GGCTCCTCCTCCTCC | 7994 |
rs3824276 | snp | A/G | 0.213575 | 0.247332 | missense | KAT6A | GRCh38.p7 | 8:42048577 | GCACTGCCTCCGAAT[A/G]ATGCAGACACATCCT | 7994 |
rs3832594 | in-del | -/TTTCA | 0 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930191 | ATTTCACGGCCCTCA[-/TTTCA]ACAGCTTCTCCTTCT | 7994 |
rs3837198 | in-del | -/TTC | | | cds-indel | KAT6A | GRCh38.p7 | 8:41937287 | CTCTTCATCTTCTTC[-/TTC]ATCTTTAGACTTCCT | 7994 |
rs3837199 | in-del | -/AACT | | | intron-variant | KAT6A | GRCh38.p7 | 8:41947242 | GCTAGTACTTCCCCT[-/AACT]GTTTTATACACTTGG | 7994 |
rs4130247 | snp | A/C | 0.271432 | 0.24908 | intron-variant | KAT6A | GRCh38.p7 | 8:41973818 | ATGTAGGAGTTGTAC[A/C]TATCCCTTAAAGGGA | 7994 |
rs4236920 | snp | A/T | 0.0854556 | 0.188216 | intron-variant | KAT6A | GRCh38.p7 | 8:42019420 | ACATTAGTAAACTGC[A/T]CTGCAGGCAGGTCAG | 7994 |
rs4327851 | snp | A/T | 0.273587 | 0.248885 | intron-variant | KAT6A | GRCh38.p7 | 8:41989322 | GAGACCAGCATGGCC[A/T]ACATGGTGAAACCCT | 7994 |
rs4454259 | snp | C/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42045884 | CAGCTACTCAGGAGG[C/T]TGAGGCAGAAGAATC | 7994 |
rs4621794 | snp | C/T | 0.00458713 | 0.047671 | intron-variant | KAT6A | GRCh38.p7 | 8:41990634 | caacctcattagtca[C/T]caagaaaatagactt | 7994 |
rs4736824 | snp | C/T | 0.499793 | 0.0101816 | intron-variant | KAT6A | GRCh38.p7 | 8:42022443 | AAATCAGGGTTAAAA[C/T]AGCCTAACAGTACAA | 7994 |
rs4737026 | snp | C/T | 0.420733 | 0.18262 | intron-variant | KAT6A | GRCh38.p7 | 8:42022307 | AAGGTTAACAGAAAT[C/T]TATCAGGTCACTGCT | 7994 |
rs4737027 | snp | A/G | 0.384593 | 0.210677 | intron-variant | KAT6A | GRCh38.p7 | 8:42023757 | ctcccaaactgctgc[A/G]actacaggtgtgagc | 7994 |
rs4737028 | snp | A/G | 0.401747 | 0.198678 | intron-variant | KAT6A | GRCh38.p7 | 8:42033447 | GATGTCTTCGAAACC[A/G]AGAGCTAAGTTAGAC | 7994 |
rs4737029 | snp | C/T | 0.424968 | 0.178567 | intron-variant | KAT6A | GRCh38.p7 | 8:42039794 | GCTGGAGTGCAGTAG[C/T]GCAATCTCGGCTCAC | 7994 |
rs4737030 | snp | A/G | 0.418491 | 0.184691 | intron-variant | KAT6A | GRCh38.p7 | 8:42039883 | GGACTACAGGCGCCC[A/G]CCACAATGCCTGGCT | 7994 |
rs5891178 | in-del | -/ATTT | | | intron-variant | KAT6A | GRCh38.p7 | 8:41943294 | TCCTATTCTCCATTT[-/ATTT]GGCTCAAATGCCTCC | 7994 |
rs6474373 | snp | G/T | 0.293294 | 0.246223 | intron-variant | KAT6A | GRCh38.p7 | 8:41940176 | ATGCTTAAAATCCAC[G/T]CCATAGCCTGGGATG | 7994 |
rs6474374 | snp | A/T | 0.0490535 | 0.14873 | intron-variant | KAT6A | GRCh38.p7 | 8:41944791 | AATGGCATATATAAC[A/T]TGTCTAATCATGAGT | 7994 |
rs6987070 | snp | A/G | 0.374 | 0.217081 | intron-variant | KAT6A | GRCh38.p7 | 8:42019799 | TATAACTCCTTCTAT[A/G]TATCATGGTTTCTTT | 7994 |
rs6988342 | snp | A/G | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42044723 | GAAATACCTGCATTA[A/G]CATCCCAGAGAAGAC | 7994 |
rs6995064 | snp | C/T | 0.419456 | 0.183806 | intron-variant | KAT6A | GRCh38.p7 | 8:42046509 | GCACTCCAGCCTGGG[C/T]GACAGAACGAGATTC | 7994 |
rs6997392 | snp | A/T | 0.040671 | 0.13668 | intron-variant | KAT6A | GRCh38.p7 | 8:42048095 | aataaaaaaaaattt[A/T]aaaaaaagttttaaa | 7994 |
rs6998779 | snp | C/T | 0.0115144 | 0.0749975 | downstream-variant-500B, intron-variant | KAT6A | GRCh38.p7 | 8:41941711 | ggggtagaaaaaaat[C/T]taagtaatctgcccc | 7994 |
rs7001139 | snp | A/G | 0.421842 | 0.181577 | intron-variant | KAT6A | GRCh38.p7 | 8:41960204 | ccagttttgcaagat[A/G]aaaaagttctggaaa | 7994 |
rs7002975 | snp | C/G | 0.372592 | 0.217879 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052726 | GAGAGGGTTCTTGGA[C/G]CTCACTAGAGCCATT | 7994 |
rs7004956 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | KAT6A | GRCh38.p7 | 8:42007130 | AAACAAATAGGAAAT[A/G]CCGTGTGCTGAAATC | 7994 |
rs7006698 | snp | A/T | 0.373799 | 0.217195 | utr-variant-5-prime | KAT6A | GRCh38.p7 | 8:42049176 | CAAAACAACCTGTTG[A/T]TTGAAATGTCTTCCA | 7994 |
rs7008039 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KAT6A | GRCh38.p7 | 8:42028749 | agctgaagacttatc[C/T]tgtattttgttaacc | 7994 |
rs7008906 | snp | A/G | 0.421209 | 0.182174 | intron-variant | KAT6A | GRCh38.p7 | 8:41989169 | AAAATACACAATCAG[A/G]TTTGGGAAGGGAAGG | 7994 |
rs7009031 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:41988500 | ACCAGGAGATAATCA[C/T]TTGGAGAAAAATAAT | 7994 |
rs7009503 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | KAT6A | GRCh38.p7 | 8:42001489 | GACTTTTCAAAAAAC[C/T]GTCTAAGACTACATT | 7994 |
rs7013640 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42044979 | GGAGAGGAAAGAAAA[G/T]AGTTAAAATACAATA | 7994 |
rs7460249 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41973486 | cggcctcccaatgtg[C/T]tgggattacaggggt | 7994 |
rs7812936 | snp | A/T | 0.499598 | 0.0141716 | intron-variant | KAT6A | GRCh38.p7 | 8:41981322 | GACTCCTTCTCAAAA[A/T]AAATAAATAAATAAA | 7994 |
rs7820342 | snp | G/T | 0 | 0 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41934563 | cttcctctcctcGGG[G/T]AGGGGCATGTCTTCT | 7994 |
rs7821579 | snp | G/T | 0.373397 | 0.217424 | intron-variant | KAT6A | GRCh38.p7 | 8:42032956 | GTCATCTCAGCTCAC[G/T]GCAAACTCTGCCTCC | 7994 |
rs7827237 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KAT6A | GRCh38.p7 | 8:42003588 | ACATCATTTTCTTTA[C/T]TGAAGTATCTAGTGT | 7994 |
rs7831915 | snp | C/T | 0.430583 | 0.172886 | intron-variant | KAT6A | GRCh38.p7 | 8:41969570 | TCTCATCCTGATCAC[C/T]GGAAAAGCCTGCAAA | 7994 |
rs7833438 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | KAT6A | GRCh38.p7 | 8:42043679 | TGCTATGAAGTTAAC[A/G]CCAAGGACATTCACG | 7994 |
rs7838607 | snp | C/T | 0.0107246 | 0.0724382 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053746 | TAAAAAAATGTTGCT[C/T]GTGAATGAACAATTT | 7994 |
rs7843105 | snp | A/G | 0.438246 | 0.16451 | intron-variant | KAT6A | GRCh38.p7 | 8:41950578 | CAGTTTCATTTTGAG[A/G]GCTAAATATTACAAC | 7994 |
rs7845738 | snp | G/T | 0.499793 | 0.0101816 | intron-variant | KAT6A | GRCh38.p7 | 8:42020909 | AAACAGCTCTGTAAC[G/T]TGATCCTTACCCTAA | 7994 |
rs9693148 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | KAT6A | GRCh38.p7 | 8:41967815 | agccctcagaaataa[C/T]gtcgcatatctacaa | 7994 |
rs9694204 | snp | C/T | 0.0554779 | 0.157039 | intron-variant | KAT6A | GRCh38.p7 | 8:41971925 | aagatgacatctctg[C/T]gggcctaagcaagta | 7994 |
rs9694612 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | KAT6A | GRCh38.p7 | 8:41967817 | ccctcagaaataacg[C/T]cgcatatctacaact | 7994 |
rs9720837 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42045579 | aaaaaaaaaaaaaaa[A/C]aaaaaaaCACTATAT | 7994 |
rs9987127 | snp | C/T | 0.392511 | 0.205404 | intron-variant | KAT6A | GRCh38.p7 | 8:42027602 | gttcataatagttgc[C/T]gacgatcctttgtac | 7994 |
rs10090379 | snp | C/T | 0.0584853 | 0.160693 | intron-variant | KAT6A | GRCh38.p7 | 8:41957382 | ACAGGGAGGAAGAAA[C/T]GGCTACACAGAAACC | 7994 |
rs10091539 | snp | A/G | 0 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930710 | TGTGTGTGTGTGTGT[A/G]TATATATATATATAT | 7994 |
rs10092480 | snp | A/T | 0.499793 | 0.0101816 | intron-variant | KAT6A | GRCh38.p7 | 8:42017073 | AAAAATTTAAAAGAC[A/T]GTATGCTGTGAAAAT | 7994 |
rs10095396 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42031906 | aaagtcctaggatta[A/C]aggcgtgagccacca | 7994 |
rs10101373 | snp | C/T | 0.0554779 | 0.157039 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053384 | AAGACACTAAATGTT[C/T]AATCGTTGACATGGA | 7994 |
rs10104089 | snp | C/G/T | 0.00312272 | 0.039391 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41941394 | TTTCTTTTCACTTTC[C/G/T]ACTGAATAAGAATCT | 7994 |
rs10104224 | snp | C/T | 0.423726 | 0.179776 | intron-variant | KAT6A | GRCh38.p7 | 8:42036566 | TGCAGTGAGCAGAGA[C/T]CGCACCACTGCACTC | 7994 |
rs10111125 | snp | C/G | 0.0554779 | 0.157039 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053468 | CACCCCGCCTAGACT[C/G]TCGCCCGCAATACCT | 7994 |
rs10111436 | snp | C/T | 0.377385 | 0.215112 | intron-variant | KAT6A | GRCh38.p7 | 8:41971174 | acatgtatacatata[C/T]gtaacaaacctgcac | 7994 |
rs10112548 | snp | G/T | 0.499866 | 0.0081858 | intron-variant | KAT6A | GRCh38.p7 | 8:42011403 | TAAATGAGACCATTT[G/T]TTCTAGAAATGAGTA | 7994 |
rs10113228 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | KAT6A | GRCh38.p7 | 8:42011964 | ggcaaactacttgaa[A/G]agacacttcaccaaa | 7994 |
rs10113248 | snp | C/T | 0.499839 | 0.00898417 | intron-variant | KAT6A | GRCh38.p7 | 8:42011288 | CTCTAAAACCACTGA[C/T]ACATTTTGCAGTCTA | 7994 |
rs10113671 | snp | A/G | 0.421368 | 0.182025 | intron-variant | KAT6A | GRCh38.p7 | 8:42036440 | ACATGATGAAACCCC[A/G]TCTCCACTAAAAAAA | 7994 |
rs10441603 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | KAT6A | GRCh38.p7 | 8:41974516 | CATGTGCTTATCTGC[A/G]AAACCAAAGCAGTTA | 7994 |
rs10464946 | snp | C/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41938540 | gagaaaaggctgatt[C/T]taggacaagggcatg | 7994 |
rs10504048 | snp | C/T | 0.304362 | 0.244018 | intron-variant | KAT6A | GRCh38.p7 | 8:41947731 | ATGAGTTCAAACAAA[C/T]TTTAAGCTGACATAC | 7994 |
rs10504049 | snp | A/G | 0.422 | 0.181428 | intron-variant | KAT6A | GRCh38.p7 | 8:41950232 | TATTCAAGAGGAACC[A/G]CTAGATAAAGAGGTT | 7994 |
rs10595164 | in-del | -/A | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42041213 | AAAAAAAAAAAAAAA[-/A]CTGTGCAGCTGATTG | 7994 |
rs10618058 | in-del | -/AC | 0.421368 | 0.182025 | intron-variant | KAT6A | GRCh38.p7 | 8:42007179 | TATTATTCTACAATG[-/AC]ACAGTTTATATAGAC | 7994 |
rs10661890 | snp | A/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41967265 | CGTCTTTCTTTTTTT[A/T]AAAAAAAAAATTTAT | 7994 |
rs10661891 | in-del | -/ATTT | | | intron-variant | KAT6A | GRCh38.p7 | 8:41967306 | TTTATTTATTTATTT[-/ATTT]TTATTATACTTTAAG | 7994 |
rs10701182 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:42006996 | AAAAAAAAAAAAAAA[-/A]TCAGTCAACTTACTC | 7994 |
rs10710765 | in-del | -/T | 0.424037 | 0.179474 | intron-variant | KAT6A | GRCh38.p7 | 8:41995675 | TCCAATTTTCATTTC[-/T]TTTTTTTTTTTTTTT | 7994 |
rs10808956 | snp | C/G | 0.421526 | 0.181876 | intron-variant | KAT6A | GRCh38.p7 | 8:42028380 | TCTCTCCCTTTAGAT[C/G]TAATAACATTTGCTT | 7994 |
rs10958705 | snp | A/G | 0.420096 | 0.183214 | intron-variant | KAT6A | GRCh38.p7 | 8:41996583 | GGCCATGAGGGCTCC[A/G]CCCTCATGACTAGAT | 7994 |
rs10958706 | snp | A/G | 0.422787 | 0.180679 | intron-variant | KAT6A | GRCh38.p7 | 8:42022010 | TTATCTCAACTCCAA[A/G]TGTGTATTTTTCTCT | 7994 |
rs11306564 | in-del | -/A | 0.421842 | 0.181577 | intron-variant | KAT6A | GRCh38.p7 | 8:42022381 | ACATAGTAACAGTTT[-/A]AAAAAAAAAATTTGA | 7994 |
rs11373085 | snp | A/C | 0.232943 | 0.249417 | intron-variant | KAT6A | GRCh38.p7 | 8:41994057 | TACTGATAATCAGTG[A/C]AAAAATCTGTGCAGA | 7994 |
rs11446895 | in-del | -/A | 0.364193 | 0.222396 | intron-variant | KAT6A | GRCh38.p7 | 8:41993004 | TAACTGCAAAAAAAA[-/A]TGGTATTCAAAATCA | 7994 |
rs11542621 | snp | C/G | | | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930929 | GCCACTCACAGGAGA[C/G]GTGCTTGTGCACTCT | 7994 |
rs11551807 | snp | A/G | | | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41929562 | AGAAAGGGGAAAAAA[A/G]GGTATTACATACAAG | 7994 |
rs11551808 | snp | A/T | 0.00279162 | 0.0372561 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41929638 | GATACAAAGGCATCT[A/T]GGCACCCCTTCCCCT | 7994 |
rs11774557 | snp | C/T | 0.38555 | 0.210062 | intron-variant | KAT6A | GRCh38.p7 | 8:42032867 | TGCTTATTTAAAACC[C/T]TGGCTTTTTTTTTTT | 7994 |
rs11775504 | snp | A/C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42033841 | ttttaattaaaaaaa[A/C/T]taaaaataaaCAAAA | 7994 |
rs11779404 | snp | C/G | 0.422 | 0.181428 | intron-variant | KAT6A | GRCh38.p7 | 8:41992704 | AAGTTGGGTTTAGAG[C/G]AATCACTGAAGAGAA | 7994 |
rs11785105 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41978349 | cagactactcggatt[C/T]tcatcccagttcaac | 7994 |
rs11786808 | snp | C/T | 0.422787 | 0.180679 | intron-variant | KAT6A | GRCh38.p7 | 8:42035561 | AGGCAAAAGATAAAA[C/T]GCCAATAAACTGAAA | 7994 |
rs11986505 | snp | C/G | 0.0637235 | 0.166737 | intron-variant | KAT6A | GRCh38.p7 | 8:42001329 | TAACACAGCACATTA[C/G]TGTCTCTGTAACTAA | 7994 |
rs11990460 | snp | A/G | 0.325563 | 0.238307 | intron-variant | KAT6A | GRCh38.p7 | 8:41980985 | GCAGAAACATGTTAC[A/G]ATCATGACTGCATAA | 7994 |
rs11990622 | snp | A/C/T | 0.0415786 | 0.138815 | intron-variant | KAT6A | GRCh38.p7 | 8:41988021 | TGTTTTCTAGCAGTA[A/C/T]GAAAAAGAAATTCCA | 7994 |
rs11991402 | snp | C/T | 0.329783 | 0.236927 | intron-variant | KAT6A | GRCh38.p7 | 8:41953330 | CTGTACTATAGTCTC[C/T]GGAACAGTTGACAGA | 7994 |
rs11993668 | snp | C/G/T | 0.0356815 | 0.128715 | intron-variant | KAT6A | GRCh38.p7 | 8:41956157 | CCTGACTTTCCAGAT[C/G/T]AGAAATTCAAACATA | 7994 |
rs11995024 | snp | A/C | 0.0633504 | 0.166319 | intron-variant | KAT6A | GRCh38.p7 | 8:41994187 | CTAATAAAAGAAAAA[A/C]GGTTGTAGCAAATGA | 7994 |
rs12114129 | snp | A/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41959180 | aaaaaaaaaaaaaaa[A/T]GTTGGAAAAGTTTCT | 7994 |
rs12114658 | snp | C/T | 0.00517208 | 0.0505894 | intron-variant | KAT6A | GRCh38.p7 | 8:41949371 | TGGGCAGCCTGTAAA[C/T]GATAATTAAACAAAA | 7994 |
rs12156252 | snp | A/G | 0.413582 | 0.189052 | intron-variant | KAT6A | GRCh38.p7 | 8:41945856 | acacggtaaaacccc[A/G]tctctagtaaaaata | 7994 |
rs12216862 | snp | C/T | 0.376592 | 0.215579 | intron-variant | KAT6A | GRCh38.p7 | 8:41970545 | CAAATATTTACTGAG[C/T]CTTTACTATATTCCA | 7994 |
rs12543005 | snp | A/C | 0.285337 | 0.248346 | intron-variant | KAT6A | GRCh38.p7 | 8:42044349 | GGTGATCCACCCCCC[A/C]CTCGGCATCCCAAAG | 7994 |
rs12543801 | snp | A/G | 0.274124 | 0.248833 | downstream-variant-500B, intron-variant | KAT6A | GRCh38.p7 | 8:41941762 | AAGATGCTGGGATAG[A/G]AAGCCTGGCAGTCTG | 7994 |
rs12545769 | snp | A/G | 0.273318 | 0.24891 | intron-variant | KAT6A | GRCh38.p7 | 8:41981344 | ATAAATAAAAGAGAT[A/G]AGTGACCATAATATT | 7994 |
rs12546107 | snp | A/G | 0.285519 | 0.247464 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050630 | AAGCCCCCTGGGAGA[A/G]TCATGCTTCAATTTG | 7994 |
rs12546563 | snp | A/C | 0.273856 | 0.248859 | intron-variant | KAT6A | GRCh38.p7 | 8:42019656 | AATTATATTCATTAC[A/C]CTAAATGATGGTAAC | 7994 |
rs12547714 | snp | A/T | 0.271432 | 0.24908 | intron-variant | KAT6A | GRCh38.p7 | 8:41952832 | AAATATAATTTTTTT[A/T]AAAAATGTAACCAAG | 7994 |
rs12548111 | snp | A/G | 0.300926 | 0.244758 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053445 | CCTGTCCCCAACCCC[A/G]TACGACACACCCCGC | 7994 |
rs12548435 | snp | A/T | 0.274393 | 0.248807 | intron-variant | KAT6A | GRCh38.p7 | 8:41954003 | TGTGCTTCCTTAAAG[A/T]TACACCACAGTGTTT | 7994 |
rs12549561 | snp | C/T | 0.272511 | 0.248984 | intron-variant | KAT6A | GRCh38.p7 | 8:41954434 | CAAAGCACCATGATG[C/T]ATTATTTCTTGTAAC | 7994 |
rs12550098 | snp | C/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41960714 | TTTTACCATTAAATA[C/T]TGACAAAATCTAGAA | 7994 |
rs12678310 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42041459 | TGTACGGCATGggcc[A/G]ggcatggtggctgac | 7994 |
rs13248721 | snp | G/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42006755 | aatcccagcacttta[G/T]gaggccgaggtgggc | 7994 |
rs13255331 | snp | C/T | 0.413748 | 0.188909 | intron-variant | KAT6A | GRCh38.p7 | 8:41945738 | TGTTTAAAAATATTT[C/T]GTGTCCAAGGCCACG | 7994 |
rs13255386 | snp | A/G | 1.68835e-05 | 0.00290542 | missense | KAT6A | GRCh38.p7 | 8:41933254 | gctgtggctgctgtg[A/G]aggcggtggtggcgg | 7994 |
rs13255395 | snp | C/G | | | missense | KAT6A | GRCh38.p7 | 8:41933257 | gtggctgctgtggag[C/G]cggtggtggcggctg | 7994 |
rs13257452 | snp | C/T | 0.290201 | 0.246747 | intron-variant | KAT6A | GRCh38.p7 | 8:41997683 | AGCTTCTCTCAAATC[C/T]ATCCCTCTACAACTA | 7994 |
rs13257587 | snp | A/C | 0 | 0 | missense | KAT6A | GRCh38.p7 | 8:41933310 | CTCTCCACCACGCAG[A/C]TCTGAGGTGACTTGA | 7994 |
rs13257588 | snp | A/C | 0.0241316 | 0.107161 | missense | KAT6A | GRCh38.p7 | 8:41933312 | CTCCACCACGCAGCT[A/C]TGAGGTGACTTGATG | 7994 |
rs13257590 | snp | C/T | 0.371785 | 0.218331 | intron-variant | KAT6A | GRCh38.p7 | 8:42020573 | GTACCTAGCATAGTG[C/T]CAGGGACATAGACGT | 7994 |
rs13257827 | snp | A/C | | | missense | KAT6A | GRCh38.p7 | 8:41933355 | GCAGGCTGGACGCTG[A/C]TCTGCTGCATCATGC | 7994 |
rs13259202 | snp | G/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42046478 | gaggcggaggttgca[G/T]tgagactgcaccact | 7994 |
rs13259238 | snp | C/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42046514 | ccagcctgggtgaca[C/G]aacgagattctgtct | 7994 |
rs13259285 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41979228 | agccgagattgcacc[A/C]ctgcattccagcctg | 7994 |
rs13260358 | snp | C/T | 0.429987 | 0.173507 | intron-variant | KAT6A | GRCh38.p7 | 8:41949857 | GGGCAAGAGGGCACA[C/T]GCTTTTTCCCAACTT | 7994 |
rs13261307 | snp | C/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42046499 | ctgcaccactgcact[C/G]cagcctgggtgacag | 7994 |
rs13262312 | snp | A/G | 0 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930809 | ACTGGTTGCACGAGA[A/G]AAAAGAGAATGGAGT | 7994 |
rs13262590 | snp | A/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42046531 | acgagattctgtctc[A/G]aaaataaataaataa | 7994 |
rs13262600 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42046537 | ttctgtctcaaaaat[A/C]aataaataaaaGCAA | 7994 |
rs13263233 | snp | A/G | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42016704 | GTAGATGGCTTTACT[A/G]TAAAGAGAGGAGGGA | 7994 |
rs13270009 | snp | C/G/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42017699 | TGCAATAAAGGCAAG[C/G/T]AAGCCCGAACCTTGT | 7994 |
rs13270093 | snp | G/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42046522 | ggtgacagaacgaga[G/T]tctgtctcaaaaata | 7994 |
rs13271030 | snp | A/C/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42016770 | AGGTCAAAACTTTGT[A/C/T]CTTAATTAGAAAAAT | 7994 |
rs13271816 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | KAT6A | GRCh38.p7 | 8:41995368 | CAGAGGGCACCAATA[C/T]TGTGTACCTTGTGTC | 7994 |
rs13272960 | snp | A/T | | | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930730 | TATATATATATATAT[A/T]TTTTTTTTTTTTTTT | 7994 |
rs13274723 | snp | A/T | 0.292266 | 0.246401 | intron-variant | KAT6A | GRCh38.p7 | 8:41968912 | CTGCAATAATTTTTT[A/T]AAAAAATTAAAACCA | 7994 |
rs13278050 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:42008354 | TAATAttttcttttt[C/T]tgagacagggtctca | 7994 |
rs13281920 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42009914 | aaaaaaaaaaaaaaa[A/C]caaaaaaaaaCAAAA | 7994 |
rs13282703 | snp | A/G | 0.331179 | 0.236453 | intron-variant | KAT6A | GRCh38.p7 | 8:41969299 | ATGACTTTCTGCACT[A/G]TATTTATGAATCCTT | 7994 |
rs13439865 | snp | G/T | 0.0700422 | 0.173537 | intron-variant | KAT6A | GRCh38.p7 | 8:42031819 | tatttttagtagaga[G/T]agggttttgtcatgt | 7994 |
rs16890946 | snp | C/T | 0.00952539 | 0.0683517 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41941187 | CCCACATTCTCCATA[C/T]TGTTCCTGAGGAGCT | 7994 |
rs16890947 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | KAT6A | GRCh38.p7 | 8:41944434 | ATCTTTCACTTCAAC[C/T]AAAACTCCTCACAAT | 7994 |
rs16890963 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | KAT6A | GRCh38.p7 | 8:41951913 | GCTACATGGAGCAGC[A/G]TAGGCCCAGTGATTA | 7994 |
rs16890974 | snp | A/T | 0.270892 | 0.249126 | intron-variant | KAT6A | GRCh38.p7 | 8:41966516 | CCTGTATAGTAGTCA[A/T]TGCTTCCTCAAAGCT | 7994 |
rs16890977 | snp | A/G | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41988316 | AAAGAAAGAAGCTAG[A/G]TAAGTTCGTGAAGAC | 7994 |
rs16890980 | snp | A/G | 0.272241 | 0.249009 | intron-variant | KAT6A | GRCh38.p7 | 8:41989023 | AGGTACCATGATAGA[A/G]CTATAGTAATAGAAA | 7994 |
rs16890984 | snp | C/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41989224 | GCTTAAAAATGCTTA[C/T]GTAGCCGGGCACAGT | 7994 |
rs16890985 | snp | C/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41992557 | ACAGGGGTGAGAGCA[C/T]GGAAAAGTCATTCTC | 7994 |
rs16890988 | snp | A/G | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41992829 | GTACTTGGCCAATCT[A/G]CTATACTTCTCAGGG | 7994 |
rs16891026 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | KAT6A | GRCh38.p7 | 8:42038963 | TGGTTTCTTCACCTG[C/T]TCCCTAATGAAGTTG | 7994 |
rs16891028 | snp | C/G | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42042069 | CTTATAAAATACCAC[C/G]ATTCTAACATATAAA | 7994 |
rs17607741 | snp | C/T | 0.244205 | 0.249933 | intron-variant | KAT6A | GRCh38.p7 | 8:41955841 | ATGGAGATGCCCTAC[C/T]GAATATGTAAGCACA | 7994 |
rs17608096 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41992569 | GCATGGAAAAGTCAT[G/T]CTCCTCGAGGGATAT | 7994 |
rs28379498 | snp | C/G | 0.0554779 | 0.157039 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052312 | GGGTTCCTCCTCTCC[C/G]GTCTCACGCGTTTAA | 7994 |
rs28396176 | snp | A/C | 0.0704125 | 0.17392 | intron-variant | KAT6A | GRCh38.p7 | 8:41980289 | AACAGGAATCAAAAG[A/C]AAAGAGTAACATTAA | 7994 |
rs28510452 | snp | A/G | 0.0840748 | 0.187 | intron-variant, missense | KAT6A | GRCh38.p7 | 8:41957056 | TCATGCACCTGCTGC[A/G]GCACTGTCTGTTGTT | 7994 |
rs28583229 | snp | A/G | 0.0554779 | 0.157039 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052900 | ATACTTAGGGCGTTG[A/G]AACCACGAGCAGGCG | 7994 |
rs28610957 | snp | G/T | 0.0554779 | 0.157039 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052822 | CGCACCTGAGCCTGG[G/T]ACTGAGATTTGTCTT | 7994 |
rs33986538 | in-del | -/AG | | | intron-variant | KAT6A | GRCh38.p7 | 8:42031039 | GCAAAAAAAAAAAAG[-/AG]GGGGGGGGGACAGGA | 7994 |
rs34011000 | in-del | -/GTAA | 0.383824 | 0.211166 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050057 | ACTGTCAAACTGCGT[-/GTAA]GTAATTCAGACAGGA | 7994 |
rs34023871 | in-del | -/T | | | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050915 | TACACGAGCGGCTAG[-/T]AGCGAGCGCAACTCG | 7994 |
rs34028057 | in-del | -/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:41994546 | AGGAAGTCACCTTCT[-/G]CAGTAAGGCTTTTTT | 7994 |
rs34084774 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42011452 | GTTAAAAATCACTAC[-/C]TTCGGCCGGGTGCGG | 7994 |
rs34120729 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41981548 | ATCAACTGACCATCC[-/C]TAAATGAATGCCTCT | 7994 |
rs34145197 | in-del | -/A/AA | | | intron-variant | KAT6A | GRCh38.p7 | 8:42007016 | AAAAAAAAAAAAAAA[-/A/AA]TCAGTCAACTTACTC | 7994 |
rs34169813 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:42044711 | CCAGGTCAATAGAAA[-/A]TACCTGCATTAGCAT | 7994 |
rs34288740 | snp | C/T | 0.3744 | 0.216852 | intron-variant | KAT6A | GRCh38.p7 | 8:41958372 | GATGAAAAAATAAGC[C/T]TCAGATAAGCCTCAG | 7994 |
rs34430323 | in-del | -/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:41949957 | CAATTCAGCACACTG[-/G]AAAGTTTCCAAGGAA | 7994 |
rs34433291 | in-del | -/G | | | frameshift-variant | KAT6A | GRCh38.p7 | 8:42048711 | TTATTATCCAATTTT[-/G]CCATGGTTCCGAGGC | 7994 |
rs34458798 | in-del | -/AAGT | | | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050059 | TGTCAAACTGCGTGT[-/AAGT]AATTCAGACAGGAAA | 7994 |
rs34469928 | snp | C/T | 0.241914 | 0.249869 | intron-variant | KAT6A | GRCh38.p7 | 8:41974050 | CTGTCTATATATTTA[C/T]GATCTTGCCATGTGT | 7994 |
rs34473679 | snp | C/T | 0.0883596 | 0.190715 | intron-variant | KAT6A | GRCh38.p7 | 8:41977384 | TACTTGTAAGGTTCC[C/T]TTTTAATACATAACA | 7994 |
rs34484119 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42036232 | ACACAGACATACATC[-/C]TTCAAGCAGAGGGCA | 7994 |
rs34506473 | in-del | -/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42026409 | ATCCATGAACAGGGG[-/G]ATGTCTTCCCATTTG | 7994 |
rs34548516 | in-del | -/T/TT | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42023505 | TTTACTTTTTTTTTT[-/T/TT]AAGACAGGGTCACAC | 7994 |
rs34554034 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:41958068 | ATTATCAGTGTGAGG[-/A]CTGGGAATGTGGGGA | 7994 |
rs34566148 | snp | A/G/T | 0.00524167 | 0.0509257 | synonymous-codon, missense | KAT6A | GRCh38.p7 | 8:41932841 | TACAGGACTGGCTCA[A/G/T]CTGGCTCCATCTCAT | 7994 |
rs34620183 | snp | A/G | 0.00586351 | 0.0538273 | missense | KAT6A | GRCh38.p7 | 8:41934643 | GTCATTGAGCCCATC[A/G]TTTCCATTCCTAAAG | 7994 |
rs34626987 | in-del | -/AT | | | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053610 | TTGCACTTACATGTG[-/AT]ATATATATATATATA | 7994 |
rs34675415 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42013261 | ATTTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTTA | 7994 |
rs34692005 | snp | C/T | 0.104938 | 0.20361 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933909 | TCAAGAAGAAAGCAG[C/T]GAGCATGAGGGCGCC | 7994 |
rs34721456 | in-del | -/ATC | | | intron-variant | KAT6A | GRCh38.p7 | 8:41948929 | ATCATCATCATCATC[-/ATC]AAGATTTACTATTAA | 7994 |
rs34758080 | in-del | -/C | | | frameshift-variant | KAT6A | GRCh38.p7 | 8:41934290 | TCGTGGTCGTCATTC[-/C]TGGGCAGTCTCTGCA | 7994 |
rs34768486 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:42002020 | AGAGATAAGACTAAA[-/A]TTCTCTCCTAATCTT | 7994 |
rs34790168 | in-del | -/A | 0.394171 | 0.204242 | intron-variant | KAT6A | GRCh38.p7 | 8:42038526 | CTAATACTATAAAGC[-/A]AGTACTACAGCATAA | 7994 |
rs34802208 | snp | G/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41992393 | TTAATGTATTCTAAG[G/T]GTTCAAGATGGGAAA | 7994 |
rs34809826 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42002016 | AACGAGAGATAAGAC[-/T]AAAATTCTCTCCTAA | 7994 |
rs34850814 | in-del | -/TAAC | 0.0505692 | 0.150756 | intron-variant | KAT6A | GRCh38.p7 | 8:42043923 | CTGTTATGTTATTAA[-/TAAC]TAACTAACCTAACAG | 7994 |
rs34851581 | snp | C/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41963710 | TGATGTCATCCACTT[C/T]TTAGAAATTCTTTAG | 7994 |
rs34869426 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:41957249 | CTTTGCACCGTGAAA[-/A]CGTTCCTGCACATGC | 7994 |
rs34871934 | in-del | -/G | | | frameshift-variant | KAT6A | GRCh38.p7 | 8:41933085 | TCATAGGAGCTGGGG[-/G]TGAAACTGTTATTCA | 7994 |
rs34897249 | in-del | -/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42017362 | ATTCTAGTAGGACAG[-/G]CAGATAAATGAACAG | 7994 |
rs34958378 | in-del | -/CAT | 0.339683 | 0.23336 | intron-variant | KAT6A | GRCh38.p7 | 8:42025366 | ACAGGTGCCCACCAC[-/CAT]GCCTGGCTAATTTTT | 7994 |
rs34989915 | in-del | -/AATA | | | intron-variant | KAT6A | GRCh38.p7 | 8:41972195 | ATGAATAAACAAATA[-/AATA]GGAAGAAGAAAAAGC | 7994 |
rs35000391 | snp | C/T | 0.151668 | 0.229849 | intron-variant | KAT6A | GRCh38.p7 | 8:42010402 | TTTCCTATGAGAAAG[C/T]AGAAATTGGGTTCAG | 7994 |
rs35094387 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42012087 | TTAGAACGGCTTTTT[-/T]AAAATGACAATATCA | 7994 |
rs35104277 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42011895 | GAAAAAAAGAAGAGG[-/C]AAAAAAAAAAAAAAA | 7994 |
rs35159084 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41961138 | AACACTGCTTACTCC[-/C]ACCTTCACTTTCAGC | 7994 |
rs35186257 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:42031033 | ATGCAAAAAAAAAAA[-/A]AGGGGGGGGGGGACA | 7994 |
rs35208851 | snp | A/G | 0.444444 | 0.157135 | intron-variant | KAT6A | GRCh38.p7 | 8:42000064 | TTCCTGAAATAGGCA[A/G]GTTCATTAAAATTTC | 7994 |
rs35321240 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42023156 | GAACAGTAAAAATAC[-/T]AATATATAAGATTTT | 7994 |
rs35408982 | in-del | -/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42012518 | AGAGGCAGAGATGGG[-/G]AGTGATGCTGCTGCT | 7994 |
rs35473387 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:41964327 | ATTTTACATATAATA[-/A]GAGGGTATCTATTAC | 7994 |
rs35520040 | in-del | -/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42014657 | TAAAGAGAAGCAAGG[-/G]AAAATAAGAAAACAG | 7994 |
rs35529154 | snp | G/T | 0.000312976 | 0.0125056 | missense, intron-variant | KAT6A | GRCh38.p7 | 8:41978656 | AAAAAACAGGTTAAA[G/T]AAACAAAACACGGTG | 7994 |
rs35594171 | in-del | -/T | 0.324382 | 0.238678 | intron-variant | KAT6A | GRCh38.p7 | 8:42003460 | AATAATTCAAACCTC[-/T]TTTTTTTTTTTTTTG | 7994 |
rs35595569 | in-del | -/A/AAGG/AG | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42031038 | TGCAAAAAAAAAAAA[-/A/AAGG/AG]GGGGGGGGGGACAGG | 7994 |
rs35601858 | in-del | -/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:41988131 | GAAACTTGTCCAAGG[-/G]ACAGTAGCTAACAAA | 7994 |
rs35646668 | snp | A/G | 0.0360663 | 0.129354 | intron-variant | KAT6A | GRCh38.p7 | 8:41948563 | GCTTTCTATCAAAAC[A/G]CCAATGGATGCCCAC | 7994 |
rs35653726 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41955862 | GTAAGCACACAAAGG[-/C]ATGATTTTTTAGTTT | 7994 |
rs35662706 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42015852 | GACGTTCACACAGGG[-/C]ATTTAAAAATAGCAA | 7994 |
rs35668345 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:42037484 | TACCCAATGACTAAG[-/A]AAAAAAGGAACCTAG | 7994 |
rs35716787 | snp | C/T | 0.151001 | 0.229563 | intron-variant | KAT6A | GRCh38.p7 | 8:42045603 | ACTATATATGAAAGC[C/T]ATGTAAGCAAATGGG | 7994 |
rs35732087 | snp | G/T | 0.234692 | 0.249531 | intron-variant | KAT6A | GRCh38.p7 | 8:42041138 | AGGCAGAGGTTGCAG[G/T]GAGCCAAGGTTGCGC | 7994 |
rs35760242 | snp | C/G/T | 0.000214399 | 0.0103517 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41934071 | TTCCCATGACACGTC[C/G/T]GTGGTGTCAGAGCAG | 7994 |
rs35872862 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:41960526 | AAAAAAAAAAAAAAA[-/A]GTCTGGTTAAAATAA | 7994 |
rs35909219 | snp | C/T | 0.379942 | 0.213577 | intron-variant | KAT6A | GRCh38.p7 | 8:41939803 | GGTGGGATCCTGGAA[C/T]AGAAAAAGGACGTTA | 7994 |
rs35918634 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41946958 | ACAGTACGCCAATGC[C/T]TAAGGATCAGCACCG | 7994 |
rs35932043 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:42028571 | TCACTTTTGGTTTCC[-/C]ATTTGCATAAAATAT | 7994 |
rs35932330 | in-del | -/T | | | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053325 | TGGCCAAGTCATGCA[-/T]TTTTTTTTTTTCTGC | 7994 |
rs35961436 | in-del | -/T | 0.49168 | 0.063958 | intron-variant | KAT6A | GRCh38.p7 | 8:42037691 | TTTTTTTTTTTTTTT[-/T]GGCTGCCAGATTTTA | 7994 |
rs35976311 | in-del | -/T | 0.413748 | 0.188909 | intron-variant | KAT6A | GRCh38.p7 | 8:41971611 | TGAGAGAACAGACTC[-/T]TTTTTTTTTTTTTTA | 7994 |
rs36067311 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42044118 | TTTTTTTTTTTTTTT[-/T]GAGATGGAGTCTTGC | 7994 |
rs36124244 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42027149 | GGTGTGTTATCTTTT[-/T]GATTGTTGCTGGATT | 7994 |
rs55824017 | snp | A/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41964804 | AAAAACAGAACAATT[A/T]AAACGATGTACTGTA | 7994 |
rs55994303 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:42007685 | TTTTTATTGTTGGCC[A/G]GGCGCAGTGGCTCAA | 7994 |
rs56121933 | in-del | -/A/AT | 0 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930729 | TATATATATATATAT[-/A/AT]TTTTTTTTTTTTTTT | 7994 |
rs56131485 | snp | A/C | 0.177824 | 0.239355 | intron-variant | KAT6A | GRCh38.p7 | 8:41947655 | TAGATGACACCTAGG[A/C]GGTGCTGCATCTTGT | 7994 |
rs56307106 | snp | C/T | | | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053936 | TATCCCGTCTCCACT[C/T]TAATCCATAGCCCTA | 7994 |
rs56345912 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41972625 | TGCACTTCAAAACTG[C/T]CAAGGTCATGAAAGA | 7994 |
rs56706199 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:41985361 | TACTATGCATAAAAA[-/A]CTGAAAAGCTAAAAA | 7994 |
rs56706985 | snp | A/G | 0.285257 | 0.247501 | intron-variant | KAT6A | GRCh38.p7 | 8:41978409 | AAAATGAAAGTAACA[A/G]CAGCAGCTATATTTC | 7994 |
rs56756690 | in-del | -/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42039914 | ATATTTTTTTTTTTT[-/T]CTTTTGTATTTTTTA | 7994 |
rs56941754 | snp | A/G | 0.271972 | 0.249033 | intron-variant | KAT6A | GRCh38.p7 | 8:42021920 | ACAGAGTAAGACTCT[A/G]TCTCAAAAACAAAAC | 7994 |
rs56965741 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41937939 | AAAGAGAAATAAAAA[C/T]ACTTTGTCTTATAGC | 7994 |
rs56985843 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KAT6A | GRCh38.p7 | 8:42021738 | GAGTTCAAGACCAGC[C/T]TGGCCAACGTGGAGA | 7994 |
rs57009251 | in-del | -/A | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41959180 | AAAAAAAAAAAAAAA[-/A]GTTGGAAAAGTTTCT | 7994 |
rs57155065 | snp | C/T | 0.273856 | 0.248859 | intron-variant | KAT6A | GRCh38.p7 | 8:42034743 | ACATGGCTCTGGCTA[C/T]CACAGAGGGCAGTAC | 7994 |
rs57721984 | snp | C/T | 0.272241 | 0.249009 | intron-variant | KAT6A | GRCh38.p7 | 8:42012388 | GATTAAATTAAGAAT[C/T]TTGAGATGGGGGGGT | 7994 |
rs58090943 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42023808 | CTTTATATCCTTATT[C/T]TACAAACTTTTCTCT | 7994 |
rs58117826 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42002613 | CAAAAAACCCACACA[A/T]AAACACAGACGAGTC | 7994 |
rs58487304 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:41975732 | ATAAAGAAAATGACA[-/A]GAGCCTATTAAAGCA | 7994 |
rs58487859 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930682 | TATATATATATATAT[A/G]TGTGTGTGTGTGTGT | 7994 |
rs58499252 | in-del | -/A | 0.374 | 0.217081 | intron-variant | KAT6A | GRCh38.p7 | 8:41948795 | ACTGTTACAGTAAGT[-/A]AACGGCACATAAGCA | 7994 |
rs58504155 | snp | C/T | 0.328616 | 0.237317 | intron-variant | KAT6A | GRCh38.p7 | 8:41998266 | AAAAAAGTAAGCCTT[C/T]TGGAAGAATCTCTGC | 7994 |
rs58970515 | in-del | -/CT | 0.372391 | 0.217992 | intron-variant | KAT6A | GRCh38.p7 | 8:41959151 | GGTGACAGAGCCAGA[-/CT]CTGTCTCGAAAAAAA | 7994 |
rs58979498 | snp | C/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41962318 | TCTACTTGATATCCC[C/T]TCTCACATCAGGTTT | 7994 |
rs59155001 | snp | C/T | | | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930655 | AATAGTTTCCATCTT[C/T]TAATGATGGAATATA | 7994 |
rs59164381 | in-del | -/CA | | | intron-variant | KAT6A | GRCh38.p7 | 8:42007182 | TATTCTACAATGACA[-/CA]GTTTATATAGACAAT | 7994 |
rs59255788 | in-del | -/TCA/TCATCA | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41948930 | TCATCATCATCATCA[-/TCA/TCATCA]AGATTTACTATTAAA | 7994 |
rs59315584 | in-del | -/A/AT | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42007987 | AAAAAAAAAAAAAAA[-/A/AT]TTTTTATTGTTAACT | 7994 |
rs59726289 | in-del | -/GACGT/TGACG | | | intron-variant | KAT6A | GRCh38.p7 | 8:41989547 | GACGTGACGTGACGT[-/GACGT/TGACG]AACATAACATAACTA | 7994 |
rs59754198 | in-del | -/AAAAC | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42021926 | TAAGACTCTGTCTCA[-/AAAAC]AAAACAAAACAAAAC | 7994 |
rs59959496 | in-del | -/AAAAAA | | | intron-variant | KAT6A | GRCh38.p7 | 8:42040755 | AAAAAAAAAAAAAAA[-/AAAAAA]GAAAGAAAGAAAGAA | 7994 |
rs60116794 | snp | A/T | 0.284471 | 0.247612 | intron-variant | KAT6A | GRCh38.p7 | 8:41969667 | ATTTTTTAATGAAAC[A/T]GATCTTGCTGTTTCC | 7994 |
rs60126106 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:41971243 | AAAAAAAAAAAAAAA[-/A]GAAAGGCCTCGTTCT | 7994 |
rs60247515 | in-del | -/AG/CA | 0.000329578 | 0.0128328 | intron-variant | KAT6A | GRCh38.p7 | 8:41946542 | ACACACACACACACA[-/AG/CA]GAGAAGGTCCACTGG | 7994 |
rs60290496 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | KAT6A | GRCh38.p7 | 8:41979933 | GAACCTGATAGGTGG[A/G]GGCTGCAGTGAGCCA | 7994 |
rs60337349 | in-del | -/TGAG | | | intron-variant | KAT6A | GRCh38.p7 | 8:41979967 | TCCTGGGCGACAGAG[-/TGAG]ACTCCATGGGTGAGG | 7994 |
rs60617375 | snp | C/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:41958666 | TATTAGTACATATAT[C/G]TGTATAGTACATGCA | 7994 |
rs60625892 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KAT6A | GRCh38.p7 | 8:42013682 | TTTTCATTCAAAACT[A/G]TCCTTGATATTTACT | 7994 |
rs60630747 | snp | A/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42005788 | CACACACACACACAC[A/T]CACACACACACTCAC | 7994 |
rs60940455 | snp | C/T | 0.271972 | 0.249033 | intron-variant | KAT6A | GRCh38.p7 | 8:42020089 | ATTCCTTTAAACTAT[C/T]TTCATATCTTATAAG | 7994 |
rs61015851 | snp | C/T | 0.303688 | 0.244167 | intron-variant | KAT6A | GRCh38.p7 | 8:41984195 | TGCTAGTCATACTCT[C/T]ACAACTCCCTCTCAT | 7994 |
rs61465627 | snp | A/G | 0.273856 | 0.248859 | intron-variant | KAT6A | GRCh38.p7 | 8:41995746 | CAATGAGGTGATCTC[A/G]GCTCACTGCAACCTC | 7994 |
rs61543371 | in-del | -/AAAA | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41991016 | AAAAAAAAAAAAAAA[-/AAAA]GGTGGAACAACACAT | 7994 |
rs61740920 | snp | A/G | 0.0204938 | 0.0991308 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933306 | AGGCCTCTCCACCAC[A/G]CAGCTCTGAGGTGAC | 7994 |
rs61753681 | snp | C/T | 3.29462e-05 | 0.00405857 | missense | KAT6A | GRCh38.p7 | 8:41932881 | GAAACACTGGTTGCA[C/T]AGGAAGTCACAGCAG | 7994 |
rs61753682 | snp | A/G/T | 0.000510535 | 0.0159693 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41934644 | TTTAGGAATGGAAAC[A/G/T]ATGGGCTCAATGACG | 7994 |
rs61753683 | snp | A/G | 6.58935e-05 | 0.00573955 | missense | KAT6A | GRCh38.p7 | 8:41937352 | GCGAAGACAAACGAC[A/G]GAAGTATTCTCTAGG | 7994 |
rs61753684 | snp | A/G | 0.00474994 | 0.0485016 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41974709 | CCAACTTTACCTGCA[A/G]TGCTTGTTCTTGGAT | 7994 |
rs62508250 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942126 | AAAAAGAGCTATAAA[A/G]GTATGCATCACATGA | 7994 |
rs62508251 | snp | C/T | 0.122064 | 0.214785 | intron-variant | KAT6A | GRCh38.p7 | 8:41946491 | CTTTAAATATATATA[C/T]ATACACACACACACA | 7994 |
rs62508252 | snp | C/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41959154 | TGACAGAGCCAGACT[C/G]TCTCGAAAAAAAAAA | 7994 |
rs62508253 | snp | C/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41959156 | ACAGAGCCAGACTGT[C/G]TCGAAAAAAAAAAAA | 7994 |
rs62508254 | snp | C/T | 0.379354 | 0.213933 | intron-variant | KAT6A | GRCh38.p7 | 8:41973294 | GGTGTGGCACGATCT[C/T]GGCTCACTGCAACCT | 7994 |
rs62510276 | snp | A/G | 0.230017 | 0.2492 | intron-variant | KAT6A | GRCh38.p7 | 8:41979132 | AATTAGCTGGGCATG[A/G]TGGTACGTGCCTGTA | 7994 |
rs62510277 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41979582 | AGTGAGATTCCAACT[A/C]CAAAAAAAAAACCTT | 7994 |
rs62510278 | snp | C/T | 0.372995 | 0.217652 | intron-variant | KAT6A | GRCh38.p7 | 8:41979771 | TTTGGGAGGCCGAGG[C/T]GAACAGATCACTTGA | 7994 |
rs62510279 | snp | A/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41980068 | TTTTCTATCAACAGG[A/T]AATTTTTTTCCAAAC | 7994 |
rs62510280 | snp | G/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41984251 | CAAGAAGATATTGCT[G/T]AAATAACACAGTGTG | 7994 |
rs62510281 | snp | C/G | 0.150333 | 0.229274 | intron-variant | KAT6A | GRCh38.p7 | 8:41989493 | CAGCCTGGGTGACAA[C/G]AGCAAGAGTCCATCT | 7994 |
rs62510282 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41989528 | AAAATAACATAACGT[A/G]ACGTGACGTGACGTG | 7994 |
rs62510283 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41990133 | AGCTTTATTCTGTAG[C/T]CTCTAAGGTACAACT | 7994 |
rs62510285 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42005296 | AGTTAATATTGCATC[A/G]AATTAAAATTTCTGA | 7994 |
rs62510287 | snp | C/G | 0.42263 | 0.180829 | intron-variant | KAT6A | GRCh38.p7 | 8:42025442 | GGTCTCGAACTCCTA[C/G]ACCTCAGGTGATCCG | 7994 |
rs66535265 | in-del | -/TCATT | 0.489142 | 0.0728777 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930188 | CTGATTTCACGGCCC[-/TCATT]TCAACAGCTTCTCCT | 7994 |
rs66657939 | in-del | -/TCA | | | intron-variant | KAT6A | GRCh38.p7 | 8:41948910 | GTCACACATCATCAT[-/TCA]CATCATCATCATCAT | 7994 |
rs66842552 | in-del | -/AAAGTAAATGCTAGCCCTCTATTTCCA | | | intron-variant | KAT6A | GRCh38.p7 | 8:41953227 | TCATTCTCTTGAACA[-/AAAGTAAATGCTAGCCCTCTATTTCCA]TTCCTGAATCTATTT | 7994 |
rs66887162 | snp | A/T | 0.330016 | 0.236849 | intron-variant | KAT6A | GRCh38.p7 | 8:41938946 | GAGTAAGACCCCATC[A/T]GGGGAAGGAAAAAAA | 7994 |
rs71239084 | in-del | -/TACACACACA | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41946493 | TTAAATATATATATA[-/TACACACACA]CACACACACACACAC | 7994 |
rs71239085 | in-del | -/A | 0.41507 | 0.187755 | intron-variant | KAT6A | GRCh38.p7 | 8:41955023 | CTCTTAAAAAAAAAA[-/A]TAAAAAAGCATTCCC | 7994 |
rs71239088 | in-del | -/TAAAAA | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41995084 | AAATAAAAATAAAAA[-/TAAAAA]CAATGCCTAGTATAT | 7994 |
rs71239089 | in-del | -/ACACACTCAC | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42005799 | CACACACACACACAC[-/ACACACTCAC]TCACTCTCTTTCTCC | 7994 |
rs71521562 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41938629 | AAACAAAAAGACCCC[A/C]CAATGACAACAACAG | 7994 |
rs71521563 | snp | A/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41953441 | ATAACAACTTATTTT[A/T]AACCTGATGAAAAAA | 7994 |
rs71521564 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41985997 | CCAGGCTGGAGTGCA[A/G]TGACGCCATCTCAGC | 7994 |
rs71521565 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42045816 | GTCTCTACTAAAAAT[A/C]CAAAAAAAAAAAAAA | 7994 |
rs71548552 | in-del | -/CAT/CATCATCAT | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41948901 | AGAGCAGAGGTCACA[-/CAT/CATCATCAT]CATCATCATCATCAT | 7994 |
rs71548553 | in-del | -/A | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41960506 | GTAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA | 7994 |
rs71548554 | in-del | -/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42009702 | CAGGAGTTCAAGACC[-/C]AGCCTGGGAAACATA | 7994 |
rs71548555 | in-del | -/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42039903 | AATGCCTGGCTAATA[-/T]TTTTTTTTTTTTCTT | 7994 |
rs71951449 | in-del | -/TAATA | | | intron-variant | KAT6A | GRCh38.p7 | 8:42041827 | TCACACTTGATAATA[-/TAATA]GCTACATTTTCCACG | 7994 |
rs71987447 | in-del | -/A | 0.495016 | 0.0496707 | intron-variant | KAT6A | GRCh38.p7 | 8:41971227 | CTTAAGGTATAATTT[-/A]AAAAAAAAAAAAAAA | 7994 |
rs72258027 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41967258 | CAAACGCGTCTTTCT[-/T]TTTTTTAAAAAAAAA | 7994 |
rs72640388 | snp | A/G | 0.052394 | 0.15314 | intron-variant | KAT6A | GRCh38.p7 | 8:41940812 | AAACTGGAATTGGAG[A/G]AAGAGAAGACCTGGA | 7994 |
rs72640392 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | KAT6A | GRCh38.p7 | 8:41953255 | GCCCTCTATTTCCAT[G/T]CCTGAATCTATTTCC | 7994 |
rs72640393 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41964316 | CTGAATATAGTATTT[C/T]ACATATAATAAGAGG | 7994 |
rs72640394 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KAT6A | GRCh38.p7 | 8:41966817 | CCCCCATGACATCCC[A/G]TATACAGAATAATGC | 7994 |
rs72640400 | snp | C/T | 0.031825 | 0.122064 | intron-variant | KAT6A | GRCh38.p7 | 8:41992388 | AGGTTTTAATGTATT[C/T]TAAGTGTTCAAGATG | 7994 |
rs72640401 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41992807 | TAACATATTTAAGTA[C/T]AGCAAAGTACTTGGC | 7994 |
rs72640402 | snp | A/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:41993415 | CAATTTGTTAAGCCA[A/G]ATAAAGGCGTTATTC | 7994 |
rs72641404 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42003461 | TTTTTTTTTTTTTTT[G/T]TTTCCCCAGCCCATG | 7994 |
rs72641407 | snp | C/T | 0.030665 | 0.119967 | intron-variant | KAT6A | GRCh38.p7 | 8:42019867 | AGCTCTTTAGGAGTT[C/T]TAACTAAAGTTCCAA | 7994 |
rs73628536 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | KAT6A | GRCh38.p7 | 8:41944736 | TACACACACACCCCC[A/G]ATCACCAAAAGTAAA | 7994 |
rs73628539 | snp | C/G | 0.0611083 | 0.163768 | intron-variant | KAT6A | GRCh38.p7 | 8:41947483 | TTATTTCAGAAGTTC[C/G]ATGTTATTACCATGG | 7994 |
rs73628541 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | KAT6A | GRCh38.p7 | 8:41973682 | GCCATTCTCCACACC[C/T]TATATTCTTTATCCT | 7994 |
rs73628543 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KAT6A | GRCh38.p7 | 8:41983567 | CCCTATTGTTAAATA[C/T]TGAGACTACGGAACA | 7994 |
rs73628546 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | KAT6A | GRCh38.p7 | 8:41989546 | GTGACGTGACGTGAC[A/G]TGACGTGACGTGACG | 7994 |
rs73628549 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41998075 | CACAGTAAGAAGTCT[A/G]GTAAATGTTACTCCT | 7994 |
rs73628551 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:41999078 | TAATTGGATCAGTAA[C/T]GATAAACTTCAATTT | 7994 |
rs73628553 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | KAT6A | GRCh38.p7 | 8:42000406 | AAATACAAAAATTAG[C/T]GGGGTGTGGTGGCAA | 7994 |
rs73628556 | snp | C/G | 0.0134861 | 0.0810011 | intron-variant | KAT6A | GRCh38.p7 | 8:42005485 | TGACAAATGCAGACT[C/G]CACACACACAATAAG | 7994 |
rs73628560 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KAT6A | GRCh38.p7 | 8:42007471 | TCTAGTTAAAGATAA[C/T]CATAAATGAATTAGT | 7994 |
rs73628563 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | KAT6A | GRCh38.p7 | 8:42013708 | TTACTTATTTATTAA[C/G]CTATTTTATCTAAAC | 7994 |
rs73628569 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | KAT6A | GRCh38.p7 | 8:42022173 | ATTCAAAATTATACA[C/G]GTTTTCAAATACAGG | 7994 |
rs73628573 | snp | A/G | 0.284471 | 0.247612 | intron-variant | KAT6A | GRCh38.p7 | 8:42036683 | TAGTGAGTGAGTGAG[A/G]ATGTGCCATAAGGCC | 7994 |
rs73628577 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | KAT6A | GRCh38.p7 | 8:42045168 | CCAACTCTAATTGAA[C/T]AGATACTATCATGAA | 7994 |
rs73628580 | snp | A/G | 0.0154538 | 0.0865337 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42049787 | ACAGTCAATAAGGCA[A/G]AAAACGACTGAGAAA | 7994 |
rs73675192 | snp | A/G | 0.0554779 | 0.157039 | intron-variant | KAT6A | GRCh38.p7 | 8:41964591 | GAATTCAGGATGCTC[A/G]ACGGCTAAGCATATG | 7994 |
rs73675193 | snp | G/T | 0.0170251 | 0.090679 | intron-variant | KAT6A | GRCh38.p7 | 8:41976047 | GTTGATCATCACTAT[G/T]GTAAAAGACCAATCA | 7994 |
rs73675195 | snp | G/T | 0.0700422 | 0.173537 | intron-variant | KAT6A | GRCh38.p7 | 8:41989762 | GGAGAAAGGTATGAA[G/T]AAGAGAGCTAAGGTG | 7994 |
rs73675198 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42021343 | CTGGAGAAAAGAGAA[A/G]GAAGTCAGCACTATT | 7994 |
rs74321368 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | KAT6A | GRCh38.p7 | 8:42023386 | AACCTTACCACAATG[C/T]AACTTTTTACATTAT | 7994 |
rs74321597 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KAT6A | GRCh38.p7 | 8:42001320 | CTTTTATTTTAACAC[A/G]GCACATTAGTGTCTC | 7994 |
rs74337152 | snp | A/G | 0.0117645 | 0.0757882 | intron-variant | KAT6A | GRCh38.p7 | 8:41949372 | GGGCAGCCTGTAAAC[A/G]ATAATTAAACAAAAA | 7994 |
rs74426135 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42000825 | AAAAATCATTATACG[C/T]TCCTCAGTTAAACAA | 7994 |
rs74496039 | snp | A/G | 0.0379877 | 0.132479 | intron-variant | KAT6A | GRCh38.p7 | 8:41996938 | GGACATATATTATAT[A/G]TTATATGATTCCATT | 7994 |
rs74522923 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053325 | TGGCCAAGTCATGCA[A/T]TTTTTTTTTTTCTGC | 7994 |
rs74547555 | snp | C/G | 0.286042 | 0.247388 | intron-variant | KAT6A | GRCh38.p7 | 8:42030165 | TCATTGGGTCTCGGA[C/G]AAGGGGGCTCCAGGC | 7994 |
rs74608813 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KAT6A | GRCh38.p7 | 8:42031468 | ATTTCTATCATCCCC[C/T]TTCTAGTTCAAACAT | 7994 |
rs74636139 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KAT6A | GRCh38.p7 | 8:42009529 | AGACGACTAATGGGT[A/G]CATGTGGGTGCATTT | 7994 |
rs74723710 | snp | A/C | | | missense | KAT6A | GRCh38.p7 | 8:41932575 | CCAGCCTGCATGGCA[A/C]CTGCCGATGGGCTAC | 7994 |
rs74738413 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:41971508 | GGTGTGTCTGAGGAA[G/T]AGGAGGCGGCTGTGG | 7994 |
rs74804345 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41966169 | TGAGTGCCAAATAAA[C/T]GTGAGCTTCTGCTTG | 7994 |
rs74806988 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050019 | ACTAAGATGTTTCTA[C/T]TCATATGCTGAAGAG | 7994 |
rs74861406 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42023829 | ACTTTTCTCTATCCA[A/C]AAAAAAAAAAAAAAA | 7994 |
rs74877332 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KAT6A | GRCh38.p7 | 8:42034970 | ATGGTCTGGTCTTTG[C/T]GCTTGTGTTCTTAAT | 7994 |
rs74942581 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | KAT6A | GRCh38.p7 | 8:42036919 | AAAGTGTGTTCATGA[A/G]GGTGTGTGTGAAGCA | 7994 |
rs74942801 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:41965862 | TGATGTCTCCTTGAT[A/G]CTGCTGAAAGTAGGA | 7994 |
rs74969791 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41976060 | ATGGTAAAAGACCAA[C/T]CAATAAAGCATACAA | 7994 |
rs74991137 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KAT6A | GRCh38.p7 | 8:41998617 | ATATACTAAGTAAGC[A/G]TTTGTTGAAATTAAA | 7994 |
rs75003800 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:42023636 | GGGACTATAGGCGCG[C/T]GCCACCATGTCCAGC | 7994 |
rs75032380 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41996428 | CCTATAACACTCAAA[C/T]ATGCACTAAGCAACA | 7994 |
rs75039781 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42031549 | AAGCTGGATCCAAAG[A/C]TGAATAATACCTATG | 7994 |
rs75063620 | snp | A/T | 0.0165278 | 0.0893908 | intron-variant | KAT6A | GRCh38.p7 | 8:42033538 | TCTAGGCCTTTGTAC[A/T]TGCTGTTCCCTTTTC | 7994 |
rs75128034 | snp | A/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42032311 | CAATCATAGCACCTG[A/G]ACTGCCTATCTTTTG | 7994 |
rs75169732 | in-del | -/TT | | | intron-variant | KAT6A | GRCh38.p7 | 8:42031946 | GTACTTTTTTTTTTT[-/TT]GAGACGGAGTCTCAC | 7994 |
rs75191777 | snp | C/T | 0.272241 | 0.249009 | intron-variant | KAT6A | GRCh38.p7 | 8:42025893 | TATGTTTTCTTCAAG[C/T]AGTTTTACAGTTTCA | 7994 |
rs75208370 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KAT6A | GRCh38.p7 | 8:41945886 | ACAAAAAAATTAGCC[A/G]GGTTGTGGTGGCTGG | 7994 |
rs75214248 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41964555 | CTCAAACGAAATGCT[C/T]GTAAGAACACTGCAG | 7994 |
rs75283259 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KAT6A | GRCh38.p7 | 8:41939706 | ACTATGAAGGCCATC[A/G]AAACTAAGGAAATTC | 7994 |
rs75346307 | snp | C/T | 0.000972658 | 0.0220314 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41934074 | CTCTGACACCACGGA[C/T]GTGTCATGGGAAGGC | 7994 |
rs75449202 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41988970 | GAGATGCTTTTAGTC[A/T]ACTGGGGAGAACAGA | 7994 |
rs75451185 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41959159 | GAGCCAGACTGTCTC[G/T]AAAAAAAAAAAAAAA | 7994 |
rs75459584 | snp | A/G | 0.146985 | 0.227789 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42049923 | AAAATAGCCTAGAGT[A/G]AAAGTGCTTACTGAA | 7994 |
rs75518560 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42044115 | TTTTTTTTTTTTTTT[G/T]TTTGAGATGGAGTCT | 7994 |
rs75568702 | snp | A/T | 0.000182226 | 0.00954358 | intron-variant | KAT6A | GRCh38.p7 | 8:41974831 | TGATTGTCTACATAT[A/T]AAAAAAGAGCTCACA | 7994 |
rs75604078 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41970107 | GTGTTTATTATCTGT[C/T]TGTTTGTGAAACTAA | 7994 |
rs75717960 | snp | C/T | 0.00398564 | 0.0444627 | downstream-variant-500B, intron-variant | KAT6A | GRCh38.p7 | 8:41941841 | GCAAAGTGAATACTA[C/T]TGTTCTTTTAAATGT | 7994 |
rs75767161 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | KAT6A | GRCh38.p7 | 8:41979987 | CTCCATGGGTGAGGG[G/T]GTGGAATAAGTGAAT | 7994 |
rs75768574 | in-del | -/TT | | | intron-variant | KAT6A | GRCh38.p7 | 8:42013084 | AGTTTTTTTTTTTTT[-/TT]AGTGGATAATGGATC | 7994 |
rs75778053 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:42004083 | TTACCTACACAGACC[A/G]TTATCTTTAGTATTT | 7994 |
rs75790682 | snp | A/G | | | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930444 | GTTTCTACCTAGCAC[A/G]CTTGAGAAAGTCAAT | 7994 |
rs75792482 | snp | A/C | 0.00028201 | 0.0118712 | missense | KAT6A | GRCh38.p7 | 8:41932542 | TTCATGCCACGCTGA[A/C]CAGCCAGTGCGCGAG | 7994 |
rs75805860 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42049456 | CCAAAACAATCATGT[A/G]TGTAAACCATTGGGA | 7994 |
rs75811135 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KAT6A | GRCh38.p7 | 8:42013764 | ATCACTCCACTGACT[A/G]CAGATTTAAAGGGAC | 7994 |
rs75855407 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41983516 | TAAACTGATCATATT[A/C]CACTGACTGATATAC | 7994 |
rs75878486 | snp | C/T | 0.0295035 | 0.117819 | intron-variant | KAT6A | GRCh38.p7 | 8:41957632 | TTATTTAAAAGAAGA[C/T]GTATGTTCCAGGCTA | 7994 |
rs75897614 | snp | A/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:42046301 | GGATCCACCTGCCTC[A/G]GCCTCCCAAAGTGCT | 7994 |
rs76010550 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:41972686 | GGAGACTAGAGAGAC[A/G]TGACAACTAAATTAG | 7994 |
rs76070933 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42009197 | TAACTACAATGTGTC[C/T]CTTTCCTTGACCATA | 7994 |
rs76075314 | snp | C/T | 0.0111196 | 0.0737302 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052591 | TCACCCCTGGCAGCT[C/T]GCCTCAGCCCCCGAC | 7994 |
rs76099702 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KAT6A | GRCh38.p7 | 8:41973803 | CCAACTCCCTACATA[C/T]CCCTTTAAGGGATAT | 7994 |
rs76142306 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42004943 | CTAAAAAAAAAAAAG[A/G]CACTATTTCTGCATA | 7994 |
rs76164429 | snp | C/G | 0.273049 | 0.248935 | intron-variant | KAT6A | GRCh38.p7 | 8:41966475 | TGGGGATCTTGGAGC[C/G]TATCACTGGTGGATA | 7994 |
rs76259148 | snp | C/G | 0.02016 | 0.0983543 | intron-variant | KAT6A | GRCh38.p7 | 8:41965829 | AAGGTACCCCCATGA[C/G]ATCTTTTTGCTGTTA | 7994 |
rs76260228 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:42006420 | TAACATCTTACGTTA[C/T]GTCACCTCAGGTTGG | 7994 |
rs76286287 | snp | A/C | 0.269809 | 0.249214 | intron-variant | KAT6A | GRCh38.p7 | 8:41991632 | TAAATTTAAATTAAT[A/C]AAAAAATATAGTATA | 7994 |
rs76335446 | snp | C/T | 0.285519 | 0.247464 | intron-variant | KAT6A | GRCh38.p7 | 8:42019416 | CAGTACATTAGTAAA[C/T]TGCACTGCAGGCAGG | 7994 |
rs76366276 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KAT6A | GRCh38.p7 | 8:41991995 | TTTTGGAAAGATAAA[A/G]TATCTACTGGAGCCT | 7994 |
rs76490242 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KAT6A | GRCh38.p7 | 8:41998340 | CATATTCCCTTTAGG[A/G]AACTCATCCTTTGTT | 7994 |
rs76596111 | snp | A/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41956212 | GCTGTTAAGGGTCTT[A/T]ACATGTTAACTCAAG | 7994 |
rs76603887 | snp | C/G | 0.0325976 | 0.123435 | intron-variant | KAT6A | GRCh38.p7 | 8:42042635 | AAGAGATTTATCATT[C/G]GATCTTTCTGCTCCA | 7994 |
rs76667400 | snp | C/G | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42009166 | ACTAGCTACATCAGA[C/G]AGAAAATCAGTTAGT | 7994 |
rs76674925 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KAT6A | GRCh38.p7 | 8:42030960 | AAGTGCATGAGCATA[C/T]ATTGTTAAGTGGTGA | 7994 |
rs76713180 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42017816 | AGTAGAGAGGGAAGC[A/T]CTCAAAGTACAGAGC | 7994 |
rs76723290 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053031 | TTTTTTTTTTTTTTT[G/T]AGACAGTGTCGCTCT | 7994 |
rs76772937 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KAT6A | GRCh38.p7 | 8:41965805 | TCAGTTTCGGCATGA[C/T]GGGATTTTAAGGTAC | 7994 |
rs77036303 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41971244 | AAAAAAAAAAAAAAA[A/G]AAAGGCCTCGTTCTC | 7994 |
rs77068899 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050633 | CCCCCTGGGAGAATC[A/T]TGCTTCAATTTGGTG | 7994 |
rs77111732 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, utr-variant-5-prime | KAT6A | GRCh38.p7 | 8:42049576 | TAAGCTACCACTAAC[C/T]AGAGTGGGTGATGGC | 7994 |
rs77135632 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:42036165 | AGTATCTACTGAAAA[C/T]GAGAAAAAAAGGTGG | 7994 |
rs77223078 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | KAT6A | GRCh38.p7 | 8:42027060 | TGATGCAATGTATCA[C/T]ATTTATTGATTTGCA | 7994 |
rs77480296 | snp | A/G | 0.0654984 | 0.168698 | intron-variant | KAT6A | GRCh38.p7 | 8:42003953 | AGTTTCCAGAATTGT[A/G]AGAAAACAAATTTCT | 7994 |
rs77496144 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:41954316 | AAGGCACTCAACATA[C/T]TGTAAGGTACTAAAT | 7994 |
rs77503253 | snp | C/T | 0.5 | 0 | missense | KAT6A | GRCh38.p7 | 8:42048623 | AACGTTCAATGCTTT[C/T]CAAAGTTGAGCCACC | 7994 |
rs77532956 | snp | A/C | 0.02016 | 0.0983543 | intron-variant | KAT6A | GRCh38.p7 | 8:41981045 | AAGAGATAAGCCAGG[A/C]GCAATGGCTCACGCC | 7994 |
rs77555310 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KAT6A | GRCh38.p7 | 8:42038714 | TGGCTGAACATTCTA[C/T]ACAATGCAGAAGATA | 7994 |
rs77575602 | in-del | -/GAAA | | | intron-variant | KAT6A | GRCh38.p7 | 8:41964627 | AATATTCCAAAATCT[-/GAAA]AAAAAAAAAAAAAAA | 7994 |
rs77578220 | in-del | -/AA | | | intron-variant | KAT6A | GRCh38.p7 | 8:42011909 | GGAAAAAAAAAAAAA[-/AA]GAATAACAAAGAGGA | 7994 |
rs77621668 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41940755 | GGAATTTCTAACTTA[C/T]ACTCTTTCAGAACTG | 7994 |
rs77687848 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KAT6A | GRCh38.p7 | 8:41971520 | GAAGAGGAGGCGGCT[A/G]TGGCTGGAGTAGCCT | 7994 |
rs77695125 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:41946890 | GCAACCATCCCAGGA[A/G]AGTAAAAATATATAA | 7994 |
rs77715516 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41951657 | CACAATGCTGATAAC[A/C]CAGCCCATGGAATCA | 7994 |
rs77717319 | snp | A/G | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41939003 | CCCAAGAGGGAAACT[A/G]AAAGAAGGAGCTTCT | 7994 |
rs77748281 | snp | A/G | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42011742 | TGAAACTCCATCTCA[A/G]AAAAAAAAAAAAGAA | 7994 |
rs77779234 | snp | A/C | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42007965 | AGACTCCGTCTCAAA[A/C]AAAAAAAAAAAAAAA | 7994 |
rs77795536 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41938163 | AATAGCTAAAATTAT[A/C]CAACTAATATCACAA | 7994 |
rs77870823 | snp | A/G | 0.273856 | 0.248859 | intron-variant | KAT6A | GRCh38.p7 | 8:42017706 | AAGGCAAGGAAGCCC[A/G]AACCTTGTCCAAAAG | 7994 |
rs77938349 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42029582 | TTGTTTTTTTTTTTT[G/T]GAAACAGGTTCTCAC | 7994 |
rs78177655 | snp | A/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41961845 | ACTGTAAAAAACCTC[A/T]AAACAATGGCCACAT | 7994 |
rs78205783 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053030 | TTTTTTTTTTTTTTT[G/T]GAGACAGTGTCGCTC | 7994 |
rs78232106 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | KAT6A | GRCh38.p7 | 8:42032259 | TCTAGTTCCATTTAT[G/T]ACCTTAACTATATAA | 7994 |
rs78262152 | snp | C/T | 0.274393 | 0.248807 | intron-variant | KAT6A | GRCh38.p7 | 8:42049431 | ATTTCCAAACTTATC[C/T]ATTAATATTCCAAAA | 7994 |
rs78292582 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:41994318 | ATCTCAGATTAAATG[C/T]CACATGAACTACAAG | 7994 |
rs78399047 | snp | A/C | 0.0111196 | 0.0737302 | intron-variant | KAT6A | GRCh38.p7 | 8:42000995 | AATCTATAGATAAAA[A/C]GTGAGGGAGGGAGAG | 7994 |
rs78449645 | snp | A/G | 0.0659589 | 0.169201 | intron-variant | KAT6A | GRCh38.p7 | 8:42021546 | TAATTTAAAGATCAA[A/G]TAACAAGTAAATGGT | 7994 |
rs78614913 | snp | A/G | 0.00719496 | 0.0595459 | intron-variant | KAT6A | GRCh38.p7 | 8:41957251 | TTTGCACCGTGAAAC[A/G]TTCCTGCACATGCGC | 7994 |
rs78636295 | snp | G/T | 0.0189856 | 0.0955633 | intron-variant | KAT6A | GRCh38.p7 | 8:42001755 | TTGAGAAGAATGAAA[G/T]TCTCCTACAACAAGG | 7994 |
rs78672953 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42029583 | TGTTTTTTTTTTTTT[G/T]AAACAGGTTCTCACT | 7994 |
rs78701071 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42000780 | GTTCTGCTATCAGAA[C/T]CATGATGTTTGGAAC | 7994 |
rs78765847 | snp | A/C | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42011820 | GAGGATTATAAAAGC[A/C]CAAATATCTTCCCAA | 7994 |
rs78804144 | snp | G/T | 0.00636936 | 0.0560724 | intron-variant | KAT6A | GRCh38.p7 | 8:41937189 | CTTTTTACTGAAGGG[G/T]CTGTCACTGCTACTG | 7994 |
rs78826062 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41949481 | AGGTTAAAAAAAAAA[C/T]TGCATATGCAAAAAT | 7994 |
rs78938806 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42046810 | TATACTTTTAATAAA[C/T]GCTCAAATTACATAG | 7994 |
rs78940422 | snp | C/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42013950 | GGTCTCTGTTAAAAC[C/T]ACTCAAGTCTGCCGC | 7994 |
rs78948177 | snp | A/G | 0.0883596 | 0.190715 | intron-variant | KAT6A | GRCh38.p7 | 8:42039604 | AAAGTATTGGCCCAC[A/G]AGTCCAGGATGAACT | 7994 |
rs78995287 | snp | A/G | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:41946146 | TGTGGCCCAGGCTAG[A/G]GCCTGCAATGCAGGG | 7994 |
rs78995461 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KAT6A | GRCh38.p7 | 8:42011035 | ATCTAATTCCCAGAT[C/T]AGTTGTCCCCAAAAA | 7994 |
rs79048121 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41961371 | ATCACCCAGCAGTTC[A/C]CCTCCTATCTTCTGC | 7994 |
rs79125012 | snp | C/T | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42046856 | GAGATTCTCTATCAA[C/T]TCATGACTGTATGAG | 7994 |
rs79155431 | snp | A/C | 0.27278 | 0.24896 | intron-variant | KAT6A | GRCh38.p7 | 8:41989681 | GACTGGTCTGGATTT[A/C]AAAATCTAGAAGTCA | 7994 |
rs79208978 | snp | A/C | 0.0162398 | 0.0886349 | intron-variant | KAT6A | GRCh38.p7 | 8:42000989 | GTGAACAATCTATAG[A/C]TAAAACGTGAGGGAG | 7994 |
rs79256613 | snp | A/T | 0.0655868 | 0.168795 | intron-variant | KAT6A | GRCh38.p7 | 8:42022957 | TGTCATTAGACAATT[A/T]CATCATTGTGCAACA | 7994 |
rs79403673 | snp | G/T | 0.294832 | 0.245947 | intron-variant | KAT6A | GRCh38.p7 | 8:41985934 | TCTTGTAAGTTTTTT[G/T]TTTGTTTGTTTGTTT | 7994 |
rs79420922 | snp | C/G | 0.0298908 | 0.118541 | intron-variant | KAT6A | GRCh38.p7 | 8:42014606 | ATCAATAAGGGGCAG[C/G]AGGTTACAGCAATAA | 7994 |
rs79547054 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41935287 | TTAGCTTATTTCCTC[C/T]TTTTTTTTCTGCTTG | 7994 |
rs79616299 | snp | A/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41951215 | CTTATTATGTGAAAA[A/T]TAGTAAACTGAAAAC | 7994 |
rs79640230 | snp | A/G | 0.271702 | 0.249056 | intron-variant | KAT6A | GRCh38.p7 | 8:41999271 | TATCTTCCTTTCACA[A/G]GTTTAGTGGTTATTT | 7994 |
rs79650387 | snp | A/C | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42023830 | CTTTTCTCTATCCAA[A/C]AAAAAAAAAAAAAAT | 7994 |
rs79716132 | snp | C/T | 0.0352966 | 0.128072 | intron-variant | KAT6A | GRCh38.p7 | 8:41951867 | TCTAAGATTATGGTA[C/T]AAGTCAAGTGAGATC | 7994 |
rs79717462 | snp | C/T | 0.0718919 | 0.175435 | intron-variant | KAT6A | GRCh38.p7 | 8:41966517 | CTGTATAGTAGTCAT[C/T]GCTTCCTCAAAGCTG | 7994 |
rs79737880 | snp | A/G | 0.273587 | 0.248885 | intron-variant | KAT6A | GRCh38.p7 | 8:41998397 | TGAATGTTCTAAAAC[A/G]TATGGTTCTCTTCCA | 7994 |
rs79832370 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41951416 | GCTGTTCTCTCACAG[A/G]AAAAAAAGATCTATC | 7994 |
rs79837210 | snp | A/G | 0.0275645 | 0.114116 | intron-variant | KAT6A | GRCh38.p7 | 8:42020046 | AGTGATGTTATCAAT[A/G]TAATTACCTTCTTTT | 7994 |
rs79990852 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KAT6A | GRCh38.p7 | 8:42010804 | GTGCCCAACCATTCT[G/T]GACACCAGATTCTTC | 7994 |
rs80020979 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | KAT6A | GRCh38.p7 | 8:42022831 | ATAAAAATGTATAAA[C/T]TATGATACACTCATA | 7994 |
rs80092286 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41993443 | TTCCAAACAGAGTCA[A/G]GCTGTATAAAAACAG | 7994 |
rs80170325 | snp | G/T | 0.5 | 0 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942099 | TGTTGAAAGGATGAA[G/T]CACTGCTTAAAAAAA | 7994 |
rs80193005 | snp | G/T | 0.28578 | 0.247426 | intron-variant | KAT6A | GRCh38.p7 | 8:42027244 | CTGTAGTTTTCTTTT[G/T]TTGTTGTTGTTGTAT | 7994 |
rs80262891 | snp | G/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053028 | ACTTTTTTTTTTTTT[G/T]TTGAGACAGTGTCGC | 7994 |
rs80263314 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41949480 | CAGGTTAAAAAAAAA[A/C]CTGCATATGCAAAAA | 7994 |
rs80273645 | snp | C/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42019762 | TACAGATATGCTTCA[C/G]TGCATACCTATACTC | 7994 |
rs80304666 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KAT6A | GRCh38.p7 | 8:41975981 | CAGATCAGGAACTTA[C/T]CTACAGGTTGATAAA | 7994 |
rs80326864 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050659 | TGGTGAGGGTCTCAA[A/G]AGGATAGAAATCAGA | 7994 |
rs80347469 | snp | A/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42022391 | AGTTTAAAAAAAAAA[A/T]TTTGATTACCTCTAA | 7994 |
rs111276929 | in-del | -/A | 0.101658 | 0.201233 | intron-variant | KAT6A | GRCh38.p7 | 8:41994056 | TACTGATAATCAGTG[-/A]AAAAAATCTGTGCAG | 7994 |
rs111284009 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41981455 | AAAGTTTCATTAGTT[C/T]CAAGTATATCCAATA | 7994 |
rs111456514 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | KAT6A | GRCh38.p7 | 8:42011526 | GTGGATCACCTGAGG[G/T]CAGGAGTTCGAGACT | 7994 |
rs111479668 | snp | A/G | | | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42051648 | GCGGGGCCGGGCGGC[A/G]GCGCGCGGGCCGCGG | 7994 |
rs111526736 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:41963563 | TGTCTCCTATCTATC[G/T]CTTCTACCTTCATTT | 7994 |
rs111526780 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41956299 | TCCATGTGTGTGAGT[A/G]CAGATATATCATGGA | 7994 |
rs111533177 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42018546 | AAAAATTATTTAATT[G/T]ACAGTCAGACCTATG | 7994 |
rs111641515 | in-del | -/T/TT | 0.571131 | 0.179171 | intron-variant | KAT6A | GRCh38.p7 | 8:42023495 | TACAAATATATTTAC[-/T/TT]TTTTTTTTTTAAGAC | 7994 |
rs111706224 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41946495 | AAATATATATATATA[C/T]ACACACACACACACA | 7994 |
rs111806051 | snp | A/C | 0.00103732 | 0.0227505 | missense | KAT6A | GRCh38.p7 | 8:41977186 | CAAGGAGACATTGCT[A/C]TCTCTGCAGAAGTCC | 7994 |
rs111917347 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41947627 | AATGTTCCTTCTATT[C/T]TTTCCAAACAGCTAG | 7994 |
rs111937762 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KAT6A | GRCh38.p7 | 8:41952816 | TCAAGCTCATTTAAG[C/T]AAATATAATTTTTTT | 7994 |
rs112108201 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | KAT6A | GRCh38.p7 | 8:42008559 | GCCCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA | 7994 |
rs112112585 | snp | A/G | | | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42051730 | GGGCGCGAGGGGGCG[A/G]CCACGGCGCCCCAGC | 7994 |
rs112178103 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:42012250 | GCAACACACCTCCTA[A/G]GTATCTGCCCAAGTC | 7994 |
rs112253411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41980043 | ATGACTACAAAGTAC[A/G]GTTAAGTCATTTTCT | 7994 |
rs112277492 | snp | A/C | 0.000150672 | 0.00867832 | missense | KAT6A | GRCh38.p7 | 8:41934365 | CTGCTCCTCCTCTGA[A/C]TGCCTCTGCTCCTCT | 7994 |
rs112333711 | snp | C/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42040013 | CGGCTTCCCAAAGTG[C/G]TGGGATTATAGGCGT | 7994 |
rs112335333 | in-del | -/A | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42044594 | AAGGTTAATATCACC[-/A]AAAAAAAAACAAAAA | 7994 |
rs112340515 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41987443 | GAAGAAAAACAGAAG[A/G]AAATCACATACCACT | 7994 |
rs112342831 | snp | A/G | 0.100944 | 0.200705 | intron-variant | KAT6A | GRCh38.p7 | 8:42021775 | ATCTCTACTAAAAAT[A/G]CAAAAATTAGGCTGG | 7994 |
rs112356841 | snp | C/T | 0 | 0 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942376 | GTCCTGAACTCCTAA[C/T]CTCAAGCAATCCTCC | 7994 |
rs112474842 | snp | C/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41938982 | AAAAAAAAAAAGCAG[C/G]AGCAGCCCAAGAGGG | 7994 |
rs112475224 | snp | C/T | 0.0410537 | 0.137264 | intron-variant | KAT6A | GRCh38.p7 | 8:41979246 | GCATTCCAGCCTGGG[C/T]GACAGAGTGAGACTC | 7994 |
rs112594715 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41969507 | TCTAAATCCATCCAC[C/T]TCTCTCCCATTTCTA | 7994 |
rs112676133 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KAT6A | GRCh38.p7 | 8:41938899 | GTTGCAGTGAGCTGA[A/G]ATCATGCCGCTGCAC | 7994 |
rs112710182 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41931240 | CAGTTAGCATTTCAA[A/G]GTACATACTAGAAAC | 7994 |
rs112735920 | snp | G/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42027201 | TTTGTGGGTGATTTT[G/T]GCATCTATGTTTTTC | 7994 |
rs112759498 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KAT6A | GRCh38.p7 | 8:41956542 | GTTTTATATAAATCC[A/G]TTTAAAGAAGCCTCT | 7994 |
rs112771325 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41990757 | CCAGCACTTTGGCAG[A/G]CCAAGGCGGGCGGAT | 7994 |
rs112842036 | snp | A/G | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42029438 | TATGGTGTCCCTCCC[A/G]TATGTCACATATGCT | 7994 |
rs113017851 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41979036 | GTCCACTGAGGCTGA[C/G]GCGGGTGGATCACCT | 7994 |
rs113095178 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41963719 | CCACTTTTTAGAAAT[A/T]CTTTAGCAGTTCCTC | 7994 |
rs113176487 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42019065 | ATGTTAGAGAATAAA[C/T]TCTCCACACAAAAAG | 7994 |
rs113176685 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:41991142 | ATCCAGCACTTCCAC[C/T]CCTAGCTATATACAC | 7994 |
rs113195648 | snp | C/T | 0.0149716 | 0.0852154 | missense | KAT6A | GRCh38.p7 | 8:41933896 | CACAGTCCTGGTAGG[C/T]GCCCTCATGCTCACT | 7994 |
rs113208074 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:42005859 | GCAGAAAAGGGAACT[A/G]CCTTTGAAAAAAAGC | 7994 |
rs113240423 | snp | A/T | 0.0131032 | 0.0799785 | intron-variant | KAT6A | GRCh38.p7 | 8:42003718 | AGCCCTAATTCCTCA[A/T]TGTGACTCTATTTGG | 7994 |
rs113246062 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41940814 | ACTGGAATTGGAGGA[A/G]GAGAAGACCTGGAAA | 7994 |
rs113273608 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42012501 | GGAGAAGACATGATG[C/T]GAAGAGGCAGAGATG | 7994 |
rs113298776 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41980473 | GCCCTCAAAAGTGCT[A/G]AGCAGTGATATAATC | 7994 |
rs113300128 | in-del | -/A | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42042444 | AAGACTCCATCTCTC[-/A]AAAAAAAAAAAAAAA | 7994 |
rs113380796 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42017235 | TTGACAGCATTGAGA[G/T]AGTAGAAGTCTGGGC | 7994 |
rs113407994 | snp | G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42029569 | TTGTAGTTTTTTTTT[G/T]TTTTTTTTTTTTTGA | 7994 |
rs113434010 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42011147 | TGCAACCCCAGACCT[A/C]ACATGCCCCTTACAT | 7994 |
rs113487546 | in-del | -/TCA | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41948928 | TCATCATCATCATCA[-/TCA]AGATTTACTATTAAA | 7994 |
rs113496780 | snp | A/G | 0.0295035 | 0.117819 | intron-variant | KAT6A | GRCh38.p7 | 8:41945747 | ATATTTCGTGTCCAA[A/G]GCCACGCATGGTGGC | 7994 |
rs113531802 | snp | A/C | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41938979 | AAAAAAAAAAAAAAG[A/C]AGCAGCAGCCCAAGA | 7994 |
rs113547013 | snp | C/G/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41980767 | CCAATTATTATTTCA[C/G/T]TTAACAAAGTAGATA | 7994 |
rs113653759 | snp | C/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42000512 | GCCGAGATCACACCA[C/T]TGCACTCCAGCCTGG | 7994 |
rs113707487 | snp | C/T | 0 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42024491 | GAAATATGCAATATA[C/T]TGCTGTTAACTACAG | 7994 |
rs113744415 | snp | C/T | 0.0298908 | 0.118541 | intron-variant | KAT6A | GRCh38.p7 | 8:42004696 | TTTGGGAGGCTGAGG[C/T]GAACAGATCACCTGA | 7994 |
rs113796071 | in-del | -/TA | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41946536 | ACACACACACACACA[-/TA]CACACAGAGAAGGTC | 7994 |
rs113798273 | snp | C/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41952323 | CTATCACCTAGGAAT[C/G]TACCTCTTTAGGATC | 7994 |
rs113809048 | snp | A/G | 0.000412041 | 0.0143475 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41934560 | CTCCTTCCTCTCCTC[A/G]GGTAGGGGCATGTCT | 7994 |
rs113950322 | snp | A/T | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:41991997 | TTGGAAAGATAAAGT[A/T]TCTACTGGAGCCTGG | 7994 |
rs113987165 | snp | A/G | 0.5 | 0 | intron-variant | KAT6A | GRCh38.p7 | 8:42047231 | CTTAAGTAAATTTAC[A/G]GCTAAGATACTAGGT | 7994 |
rs114099381 | snp | A/C | 0.00597247 | 0.0543191 | intron-variant | KAT6A | GRCh38.p7 | 8:41957516 | TAAACATGTGACTTT[A/C]CAAAGCAGCAGGTGT | 7994 |
rs114107899 | snp | C/T | 0.0170251 | 0.090679 | intron-variant | KAT6A | GRCh38.p7 | 8:42044690 | TTCATCTTCACCTTA[C/T]AGTTGGCCAGGTCAA | 7994 |
rs114254134 | snp | C/G | 0.0166325 | 0.0896639 | utr-variant-5-prime | KAT6A | GRCh38.p7 | 8:42049169 | TAGAAACCAAAACAA[C/G]CTGTTGATTGAAATG | 7994 |
rs114274608 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41964075 | GATGTCTTCCTGTTC[A/T]TTCTCACTGCAATTT | 7994 |
rs114407208 | snp | A/G | 0.0659589 | 0.169201 | downstream-variant-500B | KAT6A | GRCh38.p7 | 8:41929018 | CAAAAGGAGAATGAC[A/G]AATCTTCCTAGATTA | 7994 |
rs114429990 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | KAT6A | GRCh38.p7 | 8:41987080 | CATATGACTGTAGCC[A/C]CGTAAGGTCATACTA | 7994 |
rs114469394 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | KAT6A | GRCh38.p7 | 8:42034771 | TACAGATATAGAACA[C/T]TTCCATCATTGCACA | 7994 |
rs114576837 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42030252 | GAGGCCAGATTACAG[A/G]AGTCCATGGTGGGAA | 7994 |
rs114599683 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KAT6A | GRCh38.p7 | 8:42012645 | CTAATTTCAGACTTC[C/T]GACCCTCAGGATAGT | 7994 |
rs114645557 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050824 | TCACTCATTGTCTTT[C/T]CAGTCGGGATTGTCA | 7994 |
rs114716377 | snp | C/T | 0.0486741 | 0.148216 | intron-variant | KAT6A | GRCh38.p7 | 8:42010825 | CAGATTCTTCTTTGC[C/T]TCCCCAGGGTTTCCT | 7994 |
rs114737649 | snp | G/T | 0.0337553 | 0.125452 | intron-variant | KAT6A | GRCh38.p7 | 8:41979349 | GGAGTCCTAAGGAAA[G/T]GTTTCTTGACTGGGC | 7994 |
rs114855199 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:41937989 | GAACTATCAGTAAAG[C/T]TGTATGCCATTTTCA | 7994 |
rs114927610 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42044919 | CATCTAGGTTCGTAA[C/T]AGCAAACTATCAATT | 7994 |
rs114973782 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | KAT6A | GRCh38.p7 | 8:42003823 | ATCCTTATAAGAGAA[A/G]GAGAAATCAGGAGTG | 7994 |
rs115005779 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41982169 | AGTTAGGACCCCTCC[C/T]CACAATTTGATTATT | 7994 |
rs115024958 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41985294 | AGTTCATTCTGGTTT[C/G]TGACAACACGCTGGA | 7994 |
rs115144423 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42030875 | TAACCACTGTGCTCC[A/G]CCTCTCCGTTAAAAT | 7994 |
rs115182460 | snp | A/G | 0.0352966 | 0.128072 | intron-variant | KAT6A | GRCh38.p7 | 8:41939459 | TCATTGTGCACTACA[A/G]CCTCCAGCTCAAGTG | 7994 |
rs115236471 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:41994749 | TGTTTTTTAGGACCA[C/T]ATTCTTACTACTAAA | 7994 |
rs115238728 | snp | C/G | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42034176 | AAACAAGATAGATCT[C/G]AGGAACTGCAGGGAG | 7994 |
rs115284604 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:41940411 | CCCAAAATATAGGGC[A/T]GCACTATGTTCACTT | 7994 |
rs115327623 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | KAT6A | GRCh38.p7 | 8:41962881 | GGTCTTTGCATTTCC[C/T]GTTCCTATGCCTGGA | 7994 |
rs115368397 | snp | C/G | 0.00755907 | 0.0610114 | intron-variant | KAT6A | GRCh38.p7 | 8:41970180 | TAGTTCTGGTACCAA[C/G]GCAGGTGCATGATGC | 7994 |
rs115417716 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | KAT6A | GRCh38.p7 | 8:41985846 | CTAAATCATGGTTGT[C/T]ATCACTATAAAACAC | 7994 |
rs115567151 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41944658 | ATGTTAATTTGGAAA[C/T]GTATTACATTAGGAA | 7994 |
rs115571274 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:42016863 | AATATATTTTATATA[C/T]TACTAAACTATCCAA | 7994 |
rs115720898 | snp | C/T | 0.101301 | 0.200969 | intron-variant | KAT6A | GRCh38.p7 | 8:42016852 | CAGTTTTTCAAAATA[C/T]ATTTTATATATTACT | 7994 |
rs115745482 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KAT6A | GRCh38.p7 | 8:42031063 | GACAGGAGAAATGTA[C/T]ACATAAAGTGATCAT | 7994 |
rs115746267 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | KAT6A | GRCh38.p7 | 8:42016963 | TTATCAATATCTCTT[C/T]AATAGTTTAAGCCAC | 7994 |
rs115778864 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:41949005 | TTTCATTTAAATGCC[A/G]TATTTCATAGATTCT | 7994 |
rs115781986 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | KAT6A | GRCh38.p7 | 8:42032539 | TTCAAAGTTAATAAA[C/T]TATGAAGACAACCCA | 7994 |
rs115858429 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | KAT6A | GRCh38.p7 | 8:42042181 | AACATATCCCTGGCC[A/G]GGCACGGTGGCTCAC | 7994 |
rs115887738 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:41984096 | AAAATATCAACGTTC[A/G]TGTATCCAGCTATGC | 7994 |
rs115907281 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42035016 | TCATTTTGGCAATAA[A/T]GTGGACTAGACGAAG | 7994 |
rs115931618 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42023965 | TTTCCCCACTGGAAA[A/G]TGGGGTGATACCACA | 7994 |
rs116028414 | snp | C/T | 1.65792e-05 | 0.00287912 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942757 | ATCAAAAATATATCT[C/T]CTGTCATCAAAAATA | 7994 |
rs116033317 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:42009063 | TGTCTCAAATCACAT[A/G]TCATCATTCACCTTT | 7994 |
rs116083800 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:42049543 | GGAAACACGATGACA[C/T]GTTCTAAGAATGACC | 7994 |
rs116161849 | snp | A/G | 0.0107246 | 0.0724382 | intron-variant | KAT6A | GRCh38.p7 | 8:41991770 | ATACAGGTGATAACT[A/G]ACAGCACTCAGAACG | 7994 |
rs116181918 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | KAT6A | GRCh38.p7 | 8:41948255 | TCAAAGTACTTAACA[C/T]AACAAAAGATCTAAA | 7994 |
rs116237284 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41943268 | GTTCTGCTGCTCTTC[C/T]GCACTCTCTTTCCTA | 7994 |
rs116402915 | snp | A/G | 0.021333 | 0.101051 | intron-variant | KAT6A | GRCh38.p7 | 8:42023931 | ATCATCAATATCACT[A/G]TATTCCACTGTCCCC | 7994 |
rs116480442 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | KAT6A | GRCh38.p7 | 8:41969086 | TGATAGCCCCTCCCC[A/G]TACCATAGTTTCTAG | 7994 |
rs116492013 | snp | A/G | 0.0349115 | 0.127424 | intron-variant | KAT6A | GRCh38.p7 | 8:41964149 | AAGGCCATGGAGTCA[A/G]AATACCAGGGTTCAA | 7994 |
rs116492708 | snp | G/T | 0.0221141 | 0.102801 | intron-variant | KAT6A | GRCh38.p7 | 8:42034936 | AGCAAGTAGTCCCAG[G/T]GTGGGATAGAAAGCC | 7994 |
rs116547476 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42008257 | CAGTAACTCACAAAG[C/T]TCCCCTCATTAGGAT | 7994 |
rs116558284 | snp | C/T | 0.0648419 | 0.167978 | intron-variant | KAT6A | GRCh38.p7 | 8:41953830 | ATGAGTTAACTTGAA[C/T]GCTGAGTTCTGTAGG | 7994 |
rs116575440 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:41966635 | GATCATCTCAGGTTG[C/T]GCCAATTCTCACACA | 7994 |
rs116575953 | snp | A/G | 0.0655868 | 0.168795 | intron-variant | KAT6A | GRCh38.p7 | 8:42041554 | ACACAACTGGCCAAC[A/G]TGGTGAAACCCCATT | 7994 |
rs116634804 | snp | C/G | 0.0154538 | 0.0865337 | intron-variant | KAT6A | GRCh38.p7 | 8:41938086 | TGAAATATTTCAAAA[C/G]TAAAATAAATCTGTT | 7994 |
rs116718469 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:41950277 | ACCACAGCTACAAAT[C/T]ACAGAATGAAATGGC | 7994 |
rs116811647 | snp | A/C | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41955181 | TGGACATTTAAAAGC[A/C]CCCAGTTTCCTCAAA | 7994 |
rs116883647 | snp | G/T | 0.156319 | 0.231784 | intron-variant | KAT6A | GRCh38.p7 | 8:41987125 | TACCTTTTCTACATT[G/T]AGATATGTTTAGATA | 7994 |
rs116884365 | snp | C/T | 0.0599851 | 0.162463 | intron-variant | KAT6A | GRCh38.p7 | 8:41940261 | ACTAATTGGCTATCA[C/T]TATGATGGAATATAG | 7994 |
rs116942254 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KAT6A | GRCh38.p7 | 8:41978498 | TGGCACTTATTAAGG[A/G]CTGAATAAGTGTTAG | 7994 |
rs116968974 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42014109 | AATATTTTTCAACCA[C/T]TTAGAATTGTTAAAA | 7994 |
rs116973469 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:42021188 | AATAGATTATAAAAC[A/G]TGACAAATGGTTTTA | 7994 |
rs117102754 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:41939088 | GATTATAAAGTGAAG[C/T]ATCACGTAAATATCT | 7994 |
rs117113965 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | KAT6A | GRCh38.p7 | 8:42018976 | TAGAACAAGTTGTTC[A/G]GTGCTTAAACTGAAA | 7994 |
rs117120282 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41964593 | ATTCAGGATGCTCGA[C/T]GGCTAAGCATATGAT | 7994 |
rs117125828 | snp | A/C | 0.274393 | 0.248807 | intron-variant | KAT6A | GRCh38.p7 | 8:42021685 | CCTGTAATCCCAGCA[A/C]TTTGGGAGGCCAAGG | 7994 |
rs117129490 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41992597 | TATGTACACAATTCA[A/G]TGTAATGACCTATGA | 7994 |
rs117150462 | snp | A/G | 0.00028079 | 0.0118455 | missense | KAT6A | GRCh38.p7 | 8:41934003 | TCTTTTAATTCGATT[A/G]ACTCTTCCTTAGTGT | 7994 |
rs117157726 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KAT6A | GRCh38.p7 | 8:42044554 | AACCACTCAGCTGCC[A/G]AAAATCTAACATACA | 7994 |
rs117171922 | snp | A/G | 0.0158469 | 0.0875917 | downstream-variant-500B | KAT6A | GRCh38.p7 | 8:41929258 | CAAAGTAGGGTTACC[A/G]TGCCATGTTCCTTGG | 7994 |
rs117194624 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:42037623 | CACCTCTAGATCTGC[A/G]GAATCACCTATTCTA | 7994 |
rs117251554 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:42015022 | CTCATCTTTAAGCCT[C/T]CAGAAACACTATTTC | 7994 |
rs117270099 | snp | A/G | 0.00206736 | 0.0320844 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41932226 | TCTCATGTAAGGTCC[A/G]TTGAGTGACTGCTTG | 7994 |
rs117280306 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41947441 | GAAGATTGAAGCTGA[C/G]ACAGAACTCAGAGAG | 7994 |
rs117293745 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:42022676 | ATATCAAAATTATAA[C/T]GCCATAACACTCTTT | 7994 |
rs117322048 | snp | G/T | 0.0345262 | 0.126772 | intron-variant | KAT6A | GRCh38.p7 | 8:42003457 | CCTCTTTTTTTTTTT[G/T]TTTGTTTCCCCAGCC | 7994 |
rs117322199 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42012220 | AAGTTAAACATACCA[C/T]TACCATACAACCCAG | 7994 |
rs117334727 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41993707 | AACAAATGGTTTAAA[C/T]AAATCATCTAGGTTA | 7994 |
rs117348493 | snp | A/C | 0.000551733 | 0.0166001 | missense | KAT6A | GRCh38.p7 | 8:41933451 | GAGGACGACAGCCCA[A/C]CGTAGGAGCAGCTGC | 7994 |
rs117418169 | snp | C/T | 0.0652144 | 0.168387 | intron-variant | KAT6A | GRCh38.p7 | 8:42012909 | CTATTGACAACTACA[C/T]GGATGAATCCCAAAT | 7994 |
rs117420654 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41936619 | AGAGAAGAAATGACA[A/G]CTAGGCTGCTTTAAA | 7994 |
rs117491586 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41973853 | TTTAAGGCCCCTCAA[A/T]GAATCCTCCTCTGAC | 7994 |
rs117493933 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41988914 | AGATGCATTCATTCA[C/T]TGGTTCATTGATTTG | 7994 |
rs117524968 | snp | G/T | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:42047327 | TTACTGTTTAAGAAG[G/T]CATAATTTCAACTAT | 7994 |
rs117578611 | snp | A/G | 0.00874735 | 0.0655527 | intron-variant | KAT6A | GRCh38.p7 | 8:41958842 | AGTAACTCAGTTCAG[A/G]TCAAGTGGGACTTTA | 7994 |
rs117656187 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942072 | TTTATGTTTATTAAA[A/G]GAGGATACCGGTGTT | 7994 |
rs117665105 | snp | C/T | 0.0138799 | 0.0821421 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41931283 | GGCGTGTGTGTGCGT[C/T]ATGGCTGATTCACCA | 7994 |
rs117669248 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:41958871 | TATTGCAAAATGAGT[C/T]AGAAAAGGCCGGGCG | 7994 |
rs117728641 | snp | A/C | 0.109883 | 0.20728 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052571 | GAGGAGGCGGCTTCC[A/C]GTCCTCACCCCTGGC | 7994 |
rs117806738 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KAT6A | GRCh38.p7 | 8:42026697 | TCTACATATGAGATC[A/G]TGTTGTCTGCAAAGA | 7994 |
rs117810811 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:42006099 | ACAATTACCTTATTA[A/G]TACCTAATATACACC | 7994 |
rs117888423 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | KAT6A | GRCh38.p7 | 8:42022672 | AGGAATATCAAAATT[A/G]TAACGCCATAACACT | 7994 |
rs117978836 | snp | C/T | 0.0345262 | 0.126772 | intron-variant | KAT6A | GRCh38.p7 | 8:41940378 | AGCACCCAAGATGAG[C/T]TACTGTACTCTGAGT | 7994 |
rs118045957 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | KAT6A | GRCh38.p7 | 8:42033817 | ACCCAAACAAAACAG[C/T]TAAAAATTTTTTAAT | 7994 |
rs118048786 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41964905 | GAGGAGGAGGAGACG[A/C]TGATAATAAAATTCA | 7994 |
rs118050302 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KAT6A | GRCh38.p7 | 8:41949858 | GGCAAGAGGGCACAC[A/G]CTTTTTCCCAACTTT | 7994 |
rs118062342 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41948326 | GTAACTATGTAGTCT[A/C]ATCTATGCCAGCTGC | 7994 |
rs118069714 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:42009248 | AGATCTGCAGAACTT[A/G]AATAAAAGAACAGGA | 7994 |
rs118077503 | snp | C/T | 0.0596104 | 0.162024 | intron-variant | KAT6A | GRCh38.p7 | 8:41953760 | ATTACAGGCGTGTCC[C/T]TGGCGTATTTCTTCT | 7994 |
rs118102649 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41943637 | ATCTCATTATCACCA[A/G]GTATATCATTTATAT | 7994 |
rs118112432 | snp | G/T | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42015903 | CACACTCTAGACATA[G/T]ACTTTTCCAATTGAA | 7994 |
rs118165841 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | KAT6A | GRCh38.p7 | 8:41992797 | TTACCAAAATTAACA[A/T]ATTTAAGTATAGCAA | 7994 |
rs118167197 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42013379 | TCCTGTCTCAGCCGC[A/G]CATGCCACCAAACCC | 7994 |
rs118178283 | snp | C/T | 0.0165278 | 0.0893908 | intron-variant | KAT6A | GRCh38.p7 | 8:42048055 | AGTTTTAAAGTCTCA[C/T]GCTGGAGTACTCCTC | 7994 |
rs137881690 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:42045750 | GACCGAGGTGGGCAG[A/G]TCGCTTGAGGTCAGG | 7994 |
rs137886348 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41975996 | TCTACAGGTTGATAA[A/T]GACATGAAGAGTCTT | 7994 |
rs137943524 | snp | C/T | 1.65089e-05 | 0.00287301 | missense | KAT6A | GRCh38.p7 | 8:42048527 | CAATGGCACGTTTGA[C/T]AGCCAATCGTAACTG | 7994 |
rs137967311 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | KAT6A | GRCh38.p7 | 8:41964448 | TGAAAACTGCAGATA[A/G]TATTAAATGTTATAC | 7994 |
rs137974846 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050219 | TAAATTCAAGATTGC[C/T]GTCCTGAAACGAACA | 7994 |
rs138068162 | snp | A/C/G | 0.00318978 | 0.0398085 | intron-variant | KAT6A | GRCh38.p7 | 8:42044477 | CACACTAAAGTTCCA[A/C/G]TGTCTTCACAAAAAC | 7994 |
rs138085232 | snp | C/T | 6.63856e-05 | 0.00576094 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41940878 | TGTGAGAATTGGTGG[C/T]GAGCTTGACCGAGGG | 7994 |
rs138095271 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41991208 | TGTTCAGAGCAGCAT[C/T]ATTCATAATAATACA | 7994 |
rs138102278 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:42006159 | AAAACGAATTTTAAG[A/G]AACAGTTTAGGGACC | 7994 |
rs138113985 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:42003207 | GCATTGGCCCTTTCC[A/G]AGGAGAAACGGTTGT | 7994 |
rs138178313 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | KAT6A | GRCh38.p7 | 8:41945065 | TCTGAGGTAAAATAT[G/T]CCCTCAAATTACACA | 7994 |
rs138197397 | in-del | -/ATATATAT | 0.273856 | 0.248859 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053610 | TTGCACTTACATGTG[-/ATATATAT]ATATATATATATATA | 7994 |
rs138216579 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41994354 | GTGTGATCTGTACTC[A/C]CCTGCTTTCCCCCTC | 7994 |
rs138263675 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41976697 | GATTTCTTTAGTAAT[C/T]TGTGAAATGTAAAGT | 7994 |
rs138322320 | snp | C/T | 8.23676e-05 | 0.00641693 | missense | KAT6A | GRCh38.p7 | 8:41937348 | TCCTGCGAAGACAAA[C/T]GACGGAAGTATTCTC | 7994 |
rs138399992 | snp | C/G | 0.0017941 | 0.029897 | missense | KAT6A | GRCh38.p7 | 8:42048642 | AGTTGAGCCACCAGA[C/G]TCTGCCAAGCCCTCA | 7994 |
rs138443143 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41938878 | CTTGCATCCCAGGAG[A/G]TGGAGGTTGCAGTGA | 7994 |
rs138457957 | snp | A/G | 0.272241 | 0.249009 | intron-variant | KAT6A | GRCh38.p7 | 8:42011601 | AAAAATCAGCTGGGT[A/G]TGGTGATGCATGCCT | 7994 |
rs138464098 | in-del | -/AA | 0.00199481 | 0.0315187 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41930142 | TATAAAGAAACAAAC[-/AA]AACCAAACACAACCG | 7994 |
rs138465947 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | KAT6A | GRCh38.p7 | 8:42030487 | CCTTTGTGGAGAAGG[C/T]GAATGTTGGGGTCCT | 7994 |
rs138509182 | snp | A/G | 0.0130921 | 0.0798413 | intron-variant | KAT6A | GRCh38.p7 | 8:42024594 | TCCACCCCACCCCTC[A/G]CCCATCTCAGACTTT | 7994 |
rs138514588 | in-del | -/TTTTAA | 0.231775 | 0.249335 | intron-variant | KAT6A | GRCh38.p7 | 8:41954557 | TGATCTCATTTCATC[-/TTTTAA]TTTTAACCATAAAGA | 7994 |
rs138522256 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41970430 | AGGGCTCAGCAACCC[A/G]TTTAACTCTCTTTGG | 7994 |
rs138578452 | snp | A/C | 0.000794281 | 0.0199126 | intron-variant | KAT6A | GRCh38.p7 | 8:42048373 | GAAGCATATGCCATT[A/C]TTACCTTATCCTTTT | 7994 |
rs138608372 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41975591 | AAGTCAAGGACTCAC[C/T]GTTGACAACATTCTC | 7994 |
rs138628569 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42001658 | CACACCCAAAGAGCT[A/G]GGGCAAAAGTAAGAT | 7994 |
rs138645052 | in-del | -/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41988809 | AAACTGGTGAGTTCC[-/C]ATTTTAAATGTGTTT | 7994 |
rs138704463 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42006745 | TCATGCCTGTAATCC[C/T]AGCACTTTAGGAGGC | 7994 |
rs138707191 | snp | A/C/G/T | 0.00271618 | 0.0367525 | missense | KAT6A | GRCh38.p7 | 8:41974741 | TCACGAAATAATTCC[A/C/G/T]TATCTTTCTCAGTCA | 7994 |
rs138752654 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:41986855 | CCAGCCTGGCCAATA[C/T]GGTGAAACCTTGTCT | 7994 |
rs138758949 | snp | G/T | 1.64879e-05 | 0.00287118 | synonymous-codon | KAT6A | GRCh38.p7 | 8:42048393 | CTTATCCTTTTCATG[G/T]GGAAGAAGGGACACT | 7994 |
rs138820250 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41963665 | CATTGCTGACAATAT[C/T]ACCAGACTTGAGTTT | 7994 |
rs138836182 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41950118 | GAAACAAATAATGAC[C/T]GGCACTATAAATTAG | 7994 |
rs138840162 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:42039990 | CTGACCTCGAGATCC[A/G]CCTGCCTCGGCTTCC | 7994 |
rs138870188 | snp | A/G | 0.000399281 | 0.0141238 | downstream-variant-500B | KAT6A | GRCh38.p7 | 8:41929302 | ATCCATATTGTTGGC[A/G]TTTAAACACAGACAT | 7994 |
rs138873445 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | KAT6A | GRCh38.p7 | 8:41958535 | GTAAGTTTTTAAAAA[C/T]GGGAACTTGGTTTTC | 7994 |
rs138881873 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42017907 | TGAACTCACCGCACT[C/T]AGAAGTACCTATCAT | 7994 |
rs138912538 | snp | C/T | 1.72832e-05 | 0.00293961 | intron-variant | KAT6A | GRCh38.p7 | 8:41943998 | AAGAATCACAAATAA[C/T]TCAAATCAGAACTAG | 7994 |
rs138920610 | in-del | -/A | 0.42263 | 0.180829 | intron-variant | KAT6A | GRCh38.p7 | 8:42025441 | TGGTCTCGAACTCCT[-/A]CACCTCAGGTGATCC | 7994 |
rs138944476 | snp | A/C/T | 3.29766e-05 | 0.00406045 | missense, stop-gained | KAT6A | GRCh38.p7 | 8:41934112 | CTTCGGAATCCAGCT[A/C/T]GGTTTCCTCTTTATC | 7994 |
rs138999142 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41971069 | CACACACCGGGGCCT[A/G]TTGTGGGGTGGGAGG | 7994 |
rs139023849 | in-del | -/T | 0.108048 | 0.20579 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052583 | TCCCGTCCTCACCCC[-/T]GGCAGCTCGCCTCAG | 7994 |
rs139040442 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41953752 | GTGCTGGGATTACAG[A/G]CGTGTCCTTGGCGTA | 7994 |
rs139076845 | in-del | -/CTC | 0.000562095 | 0.016755 | cds-indel | KAT6A | GRCh38.p7 | 8:41940902 | CCGAGGGCTTTCCGG[-/CTC]CTCCTCCTCCTCGCT | 7994 |
rs139106027 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:42030962 | GTGCATGAGCATATA[C/T]TGTTAAGTGGTGAGA | 7994 |
rs139138850 | snp | A/G | 8.23635e-05 | 0.00641677 | missense | KAT6A | GRCh38.p7 | 8:41941078 | GTCTTCTCTTGGGAA[A/G]GTCAGGTTTCCCGTC | 7994 |
rs139151187 | snp | A/T | 1.65105e-05 | 0.00287315 | missense | KAT6A | GRCh38.p7 | 8:41974813 | TTGCCATCCCAGCCA[A/T]CCTGATTGTCTACAT | 7994 |
rs139168783 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42036771 | ACTTTCTCGCAACTA[C/T]ATACCACACAAGATC | 7994 |
rs139211089 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:42021695 | CAGCACTTTGGGAGG[C/T]CAAGGCAGGTAGATT | 7994 |
rs139231999 | snp | A/C | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41984809 | AGAGATGGTGAAACC[A/C]CACCTCTACTAAAAA | 7994 |
rs139244390 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41981225 | CAGAAGGCTGAGGCA[C/G]GAGAACTGCTTGAAC | 7994 |
rs139246249 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KAT6A | GRCh38.p7 | 8:42036010 | AGAGATGAGCCTTTC[A/G]CACTTCTTTCACTGT | 7994 |
rs139283571 | snp | A/C | | | intron-variant | KAT6A | GRCh38.p7 | 8:41987741 | CTGGCTGGGCCTTTA[A/C]AACTGGTCCTTGTTA | 7994 |
rs139285897 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41966338 | TTTATCATCTCACAC[C/T]GTCAGAAGAGTTAGT | 7994 |
rs139350181 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:41983133 | AGTCAGTTATCAGTC[C/T]GATTCTCAAAAATTA | 7994 |
rs139386888 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:42045921 | ACCCGGGAGGCGAAG[A/G]TTGCAGTGAGCTGAG | 7994 |
rs139391865 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:41961005 | AACAGAGAATCATGC[C/T]ACCCAGTCTCACATT | 7994 |
rs139394106 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41936564 | AAAAGACTTGTTTCT[C/G]ACCTGGCTCATATAT | 7994 |
rs139429467 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41992531 | CTCTCCACTACACCA[A/T]CTTTTATAAAACAGG | 7994 |
rs139493594 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42041804 | AATATAACAATTACT[A/G]AGATCAATCCATTTC | 7994 |
rs139494583 | snp | C/T | 9.89299e-05 | 0.00703244 | missense | KAT6A | GRCh38.p7 | 8:41934559 | CCTCCTTCCTCTCCT[C/T]GGGTAGGGGCATGTC | 7994 |
rs139521884 | snp | C/T | 0.02016 | 0.0983543 | intron-variant | KAT6A | GRCh38.p7 | 8:41996224 | AAAAAACTGCACTTG[C/T]AAACTCAAACTCATA | 7994 |
rs139545895 | in-del | -/T | 0.00755907 | 0.0610114 | intron-variant | KAT6A | GRCh38.p7 | 8:41944395 | CTATTAAAATTGTAG[-/T]TTCTGTCAGTGAATT | 7994 |
rs139556026 | snp | A/G | 6.64165e-05 | 0.00576228 | intron-variant | KAT6A | GRCh38.p7 | 8:41978806 | AAATTCCACATAGAA[A/G]TGTGACAGACATAAA | 7994 |
rs139564445 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:41940587 | AAAAGTTTGTTTGCA[A/T]CCCAGGAGGTGAAGC | 7994 |
rs139570614 | snp | C/T | 0.00835141 | 0.0640778 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053458 | CCATACGACACACCC[C/T]GCCTAGACTGTCGCC | 7994 |
rs139582518 | in-del | -/T | 0.499631 | 0.0135733 | intron-variant | KAT6A | GRCh38.p7 | 8:41967257 | ACAAACGCGTCTTTC[-/T]TTTTTTTAAAAAAAA | 7994 |
rs139594433 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41991687 | CTTCAAGAAACATCA[A/G]TAGTGATTTGGACAT | 7994 |
rs139670708 | snp | G/T | 0.0138799 | 0.0821421 | intron-variant | KAT6A | GRCh38.p7 | 8:42008291 | CCAAAGCTAACATTT[G/T]CAACTCCAAAAATCC | 7994 |
rs139673201 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | KAT6A | GRCh38.p7 | 8:41936018 | TGTAATCCCAGCACT[C/T]TGGGAGTCCAAGGCG | 7994 |
rs139721599 | in-del | -/ACAT | 0.0615074 | 0.164338 | intron-variant | KAT6A | GRCh38.p7 | 8:41946529 | CACACACACACACAC[-/ACAT]ACACACACACACAGA | 7994 |
rs139727263 | snp | G/T | 0.0115144 | 0.0749975 | intron-variant | KAT6A | GRCh38.p7 | 8:42004342 | CAGGAAAAAAAGAAG[G/T]AGGAGCACACTTATT | 7994 |
rs139731056 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42008843 | AAATAGCTACATGCA[A/C]CTAATGGCAACTGTA | 7994 |
rs139877562 | snp | C/T | 1.64741e-05 | 0.00286998 | missense | KAT6A | GRCh38.p7 | 8:41940954 | AGGACAGCCCTGTCA[C/T]CCTCACTGTAGCGAC | 7994 |
rs139919200 | snp | A/G | 0.0197687 | 0.0974348 | intron-variant | KAT6A | GRCh38.p7 | 8:41977607 | CTAGCTGTACGACTT[A/G]GACAAATCACATTTT | 7994 |
rs139920738 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:41936808 | GCTCTTTCTGGAGAA[C/T]TGTCTTCTTAGCATT | 7994 |
rs139939916 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:42028424 | GCTCCTATATTGGGT[A/G]CGTATATATTTACCA | 7994 |
rs139942484 | snp | C/T | 3.29468e-05 | 0.00405861 | missense | KAT6A | GRCh38.p7 | 8:41941248 | TCTTTATCACCAAAA[C/T]GTTCCTGGGTTTTTC | 7994 |
rs139944664 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42003916 | GAGGATAACCTTGCC[A/G]GTGCCTTGATTTGCA | 7994 |
rs139955916 | snp | C/T | 0.00318978 | 0.0398085 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41929610 | GCTGGCCCAGGAGCG[C/T]GTGACATGGAGAGAT | 7994 |
rs139984164 | snp | G/T | 0.0158469 | 0.0875917 | intron-variant | KAT6A | GRCh38.p7 | 8:42032141 | TTGCCGTGTTAGCCA[G/T]GAGTACTTGTTTTTT | 7994 |
rs139991454 | in-del | -/TCTG | 0.370772 | 0.218893 | intron-variant | KAT6A | GRCh38.p7 | 8:41970102 | TATGAGTGTTTATTA[-/TCTG]TCTGTTTGTGAAACT | 7994 |
rs140066687 | snp | C/T | 0.0162398 | 0.0886349 | intron-variant | KAT6A | GRCh38.p7 | 8:41937651 | AGTTTTAAAACCAAA[C/T]AGAATTAGCACATAT | 7994 |
rs140089536 | in-del | -/A | 0.27008 | 0.249192 | intron-variant | KAT6A | GRCh38.p7 | 8:41971897 | CAGAGAAAAAAAAAA[-/A]TCAAGATGACATCTC | 7994 |
rs140120011 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | KAT6A | GRCh38.p7 | 8:41965290 | CATAATTTTCACATG[C/T]CCATAAATATTATTC | 7994 |
rs140126559 | snp | A/T | 0.000132762 | 0.00814639 | missense | KAT6A | GRCh38.p7 | 8:41977306 | AGGGCCAGTTCGAAC[A/T]TTGCTGAAGGGACCT | 7994 |
rs140133665 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41989101 | ACTTAAGTTTTTCCA[C/G]AAGTATTTAACAGGC | 7994 |
rs140152757 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41961511 | TGTAATCCTAACACT[C/T]TGGGAGGCCAAGGTG | 7994 |
rs140193334 | snp | C/T | 0.0115144 | 0.0749975 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052660 | GGAACCAGAAGCACC[C/T]GTCTTAACCCCTTTC | 7994 |
rs140194943 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42010822 | CACCAGATTCTTCTT[C/T]GCTTCCCCAGGGTTT | 7994 |
rs140223219 | snp | A/C/T | 0.000115305 | 0.0075922 | missense | KAT6A | GRCh38.p7 | 8:41934621 | TGGATCTTGGGTTTA[A/C/T]GTCCAGCTTTAGGAA | 7994 |
rs140250689 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KAT6A | GRCh38.p7 | 8:42023098 | GAATATTGAAGGCAA[C/T]TGTAACACAATGGTA | 7994 |
rs140264396 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41979166 | CCAGCTACTCGGGAG[C/G]CTAAGGCAGGAGAAT | 7994 |
rs140266175 | snp | A/G | 0.00614398 | 0.055084 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41932307 | CATGTTCCCATGAGG[A/G]TTAGGCTGCATAGGC | 7994 |
rs140266345 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | KAT6A | GRCh38.p7 | 8:41946867 | AAGTCACTGCCATTA[C/T]CCACAAAGCAACCAT | 7994 |
rs140282110 | in-del | -/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42023502 | AATATATTTACTTTT[-/T]TTTTTTAAGACAGGG | 7994 |
rs140297976 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | KAT6A | GRCh38.p7 | 8:42028904 | GTGAGTTTTATGTAT[C/T]TGCATGTTTTCATGG | 7994 |
rs140298853 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KAT6A | GRCh38.p7 | 8:41975770 | ACACCACTGTCAAAA[A/G]TTCAATATTGGTTCT | 7994 |
rs140342559 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41997883 | TGATAAACATCTACT[A/G]ACAAGCACTCTACTA | 7994 |
rs140344063 | snp | C/T | 3.2975e-05 | 0.00406035 | missense | KAT6A | GRCh38.p7 | 8:42048436 | GAAAGAGACTCACAA[C/T]TCTCTTTCCCATCCA | 7994 |
rs140382955 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41953520 | CTCCTGTTGCCCAGG[C/T]GAGAGTGCAATGGCG | 7994 |
rs140452329 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41957475 | GGTCTTTTTATTTTA[A/G]CATTTCAACCAAAGT | 7994 |
rs140541051 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42044420 | AACTTTTAATCACAG[C/T]ATCCCATGGATTCTC | 7994 |
rs140555768 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41948235 | TTAGATAGCAAGTTT[C/T]GTTTTCAAAGTACTT | 7994 |
rs140560177 | snp | A/T | 0.000230627 | 0.0107359 | missense | KAT6A | GRCh38.p7 | 8:41933035 | TCTCATAGATACTTA[A/T]GTTCCCAGTGCTTCC | 7994 |
rs140562342 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42015019 | CTCCTCATCTTTAAG[C/T]CTCCAGAAACACTAT | 7994 |
rs140568413 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:42039520 | GAAGACTGAATGATA[C/T]AAATTTTCTTTCCAG | 7994 |
rs140618850 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41994193 | AAAGAAAAAAGGTTG[C/T]AGCAAATGACTTTAC | 7994 |
rs140619686 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42046599 | AATTCACAGGTATGG[A/C]ACTGAACTGATCTAA | 7994 |
rs140666969 | snp | A/C/T | 9.92453e-05 | 0.00704377 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41932619 | CTGCTGGTGAGCAGC[A/C/T]GCAGAGGGCAGTGGC | 7994 |
rs140691056 | snp | G/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42026255 | CTTTGGCTACTCAGG[G/T]TCTTTTGTGGTTCCG | 7994 |
rs140691340 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KAT6A | GRCh38.p7 | 8:41973481 | CGCCTCGGCCTCCCA[A/G]TGTGCTGGGATTACA | 7994 |
rs140741971 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | KAT6A | GRCh38.p7 | 8:42034085 | ACTAAGTCTGCAAGG[C/T]TGAAGAGCTAATTTA | 7994 |
rs140750938 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41969992 | CTCATAAACACTCCA[A/T]CCCCAACCCTCAGCA | 7994 |
rs140754789 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42019667 | TTACCCTAAATGATG[A/G]TAACTGATTGAGTAT | 7994 |
rs140780968 | snp | C/T | 0.000428251 | 0.0146268 | missense | KAT6A | GRCh38.p7 | 8:41977214 | TCCAAGCCATCTATC[C/T]GCTCTAAATATCCTT | 7994 |
rs140788886 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:41983961 | CTTTGGACTTCATGC[C/T]TAGAAATGTAAACAT | 7994 |
rs140852179 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42022065 | ATTCTAATATACTAC[A/G]GCAAATCGTTTGACC | 7994 |
rs140881210 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | KAT6A | GRCh38.p7 | 8:42047226 | AGCACCTTAAGTAAA[C/T]TTACAGCTAAGATAC | 7994 |
rs140894504 | snp | C/T | 0.000181194 | 0.00951651 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41932979 | GCTGAAGGTGGCTGA[C/T]GGTTGAGAGTAGCTG | 7994 |
rs140919839 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:42016056 | CCCCAGAAACTGCAC[A/G]TTAACAGCAGTGCTT | 7994 |
rs140974853 | snp | A/C | 0.0174175 | 0.0916809 | intron-variant | KAT6A | GRCh38.p7 | 8:42037445 | TTAAAGGTTCTAGAA[A/C]ACTCAGGAGTTAAAT | 7994 |
rs140989699 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42043633 | CACAATGAAGACGGG[C/T]GGGAATTTGTCCTTT | 7994 |
rs141004007 | in-del | -/AAAT | 0.273049 | 0.248935 | intron-variant | KAT6A | GRCh38.p7 | 8:41972194 | ACAAAATGAATAAAC[-/AAAT]AAATAGGAAGAAGAA | 7994 |
rs141063615 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41993951 | AATGCACTAAGGTGG[C/T]TATAGGAAAAATAGA | 7994 |
rs141136227 | snp | G/T | 0.02016 | 0.0983543 | intron-variant | KAT6A | GRCh38.p7 | 8:42003629 | TAATATCTTAGCAAC[G/T]TGGCATACCTACCTA | 7994 |
rs141160181 | in-del | -/ATACA | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41953894 | ATACATATACAATAC[-/ATACA]ATACATGTATAATAT | 7994 |
rs141272619 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41996085 | CTAACTTTATTTTGT[C/T]TCTATTCTTAAACAC | 7994 |
rs141360124 | snp | C/T | 0.0217134 | 0.101908 | utr-variant-5-prime | KAT6A | GRCh38.p7 | 8:42048994 | GTGAAGGATTCTGTA[C/T]ATCCATAGAGTCGTT | 7994 |
rs141380756 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | KAT6A | GRCh38.p7 | 8:41946313 | TTGCCATGTTGCCTA[A/C]GCTGGTCTTGAACTA | 7994 |
rs141395236 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41974051 | TGTCTATATATTTAC[A/G]ATCTTGCCATGTGTC | 7994 |
rs141460530 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | KAT6A | GRCh38.p7 | 8:41969201 | TGCTGTAAGACTACC[A/G]AAGACACTGTAATAA | 7994 |
rs141473078 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:42031372 | CTAGAATACATCTGA[C/T]ACCCTATTTTCTCCT | 7994 |
rs141486173 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41939642 | TATATTACCCCATTC[A/T]AATATCATGAGGGAT | 7994 |
rs141564825 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41970519 | ATTTCATTCAATATC[C/G]ATTCATTAAACAAAT | 7994 |
rs141582082 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42023383 | GTTAACCTTACCACA[A/T]TGTAACTTTTTACAT | 7994 |
rs141610909 | snp | C/T | 0.00016608 | 0.00911111 | missense | KAT6A | GRCh38.p7 | 8:41934828 | GAATTCTTCACATCA[C/T]GTTTTCGCAAAAGAG | 7994 |
rs141641517 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | KAT6A | GRCh38.p7 | 8:41960186 | TTTAATGGGTACAGA[C/G]TTCCAGTTTTGCAAG | 7994 |
rs141667008 | snp | A/G | 3.29592e-05 | 0.00405938 | synonymous-codon | KAT6A | GRCh38.p7 | 8:42048573 | GGCAGCACTGCCTCC[A/G]AATAATGCAGACACA | 7994 |
rs141667969 | snp | C/T | 9.88354e-05 | 0.00702908 | missense | KAT6A | GRCh38.p7 | 8:41940963 | CTGTCACCCTCACTG[C/T]AGCGACGGGGCAGCC | 7994 |
rs141724678 | snp | A/G | 0.000132026 | 0.00812377 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41941364 | TGTAGAACTGACTGG[A/G]GCCATAACTTCTGGT | 7994 |
rs141739124 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41974773 | GATTTCCTGGCTCCC[A/G]AAAAGTCGCTCCTCA | 7994 |
rs141745062 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41952310 | TTCCTAGGCTACTCT[A/G]TCACCTAGGAATCTA | 7994 |
rs141773007 | snp | A/G | 4.95029e-05 | 0.00497484 | missense | KAT6A | GRCh38.p7 | 8:41955375 | TGACAGAGGGACAGC[A/G]GACTTGTGGATCAGG | 7994 |
rs141811874 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41992767 | ACTGAGAACAGTATC[A/G]CAACTCAAACTAAAT | 7994 |
rs141841929 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42040274 | TGATACAGAGCAAAG[A/G]AAAAACGAGGTTAAG | 7994 |
rs141843993 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41986893 | AAATATAAAAATTAG[A/C]CAGGTGTGGTGGCAG | 7994 |
rs141851127 | snp | C/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41938193 | AAATAAGAGATGATG[C/T]CCCAGAGATTATCTA | 7994 |
rs141853755 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:42036339 | AGAGAGGTTGGGCAC[A/G]ATGGCTCATGCCTGT | 7994 |
rs141877916 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KAT6A | GRCh38.p7 | 8:41989458 | AGGTTGTAGTGAGCC[A/G]AGATCGCACCATTGC | 7994 |
rs141898282 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41985749 | TTGCTTCTTCAGCCC[C/T]GACAATGATTTCACA | 7994 |
rs141965893 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942655 | TTCTTGAAATCTCTA[A/C]CACTGAAATAAAACT | 7994 |
rs141983281 | snp | C/T | 0.0655868 | 0.168795 | intron-variant | KAT6A | GRCh38.p7 | 8:41990932 | CCTGGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA | 7994 |
rs142002726 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050733 | AAACTAAATGAGAAG[C/G]TACATCCTGAGTTTA | 7994 |
rs142017067 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:41980087 | TTTTTTCCAAACAAA[A/T]ATTATGAAATATCCT | 7994 |
rs142115612 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KAT6A | GRCh38.p7 | 8:41988811 | AACTGGTGAGTTCCA[C/T]TTTAAATGTGTTTAG | 7994 |
rs142174569 | in-del | -/ACACACAC | | | intron-variant | KAT6A | GRCh38.p7 | 8:42005764 | ATGCTGCAAGCAAAT[-/ACACACAC]ACACACACACACACA | 7994 |
rs142196244 | snp | A/C | 0.000798403 | 0.0199641 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41931505 | CACTTGATTCAAGAA[A/C]AACAAAGATTTCAAT | 7994 |
rs142198905 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | KAT6A | GRCh38.p7 | 8:42006258 | CTGGGAGTATGTTAT[A/G]TGTGTGTGTGCAGGT | 7994 |
rs142223557 | snp | C/G | 0.000593709 | 0.0172192 | intron-variant | KAT6A | GRCh38.p7 | 8:41981968 | GCCTAATACGAGGGA[C/G]AACATTCATGAATGA | 7994 |
rs142225338 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | KAT6A | GRCh38.p7 | 8:41962806 | GCCTTATGTATTTGG[C/T]TCTAGTCACACTGGC | 7994 |
rs142254138 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42005343 | CTTCAATACTACCTC[C/T]GTAACAGTATAAATA | 7994 |
rs142290678 | snp | A/T | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:42010157 | TAAAAATACAAAAAT[A/T]AGCTTGGTGTGGTCG | 7994 |
rs142330684 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42013650 | TATCCTAACCAAGAT[G/T]AATGGTCCTTCTATA | 7994 |
rs142375598 | snp | C/T | 0.000153988 | 0.00877328 | missense | KAT6A | GRCh38.p7 | 8:41942911 | GGAGTCCAGCGCAAA[C/T]ATTCTGGATCTACAT | 7994 |
rs142386289 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | KAT6A | GRCh38.p7 | 8:42000564 | TCAAAAAAACAGAAG[A/G]AAAAAAAAAGAAAAA | 7994 |
rs142396933 | snp | G/T | 1.64779e-05 | 0.00287031 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41980865 | TGGCATACGGGTGAG[G/T]GGCGGATCACAACAC | 7994 |
rs142482075 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41947680 | TCTTGTTGTGTCCCC[A/G]AGTGAGAACCAGCAA | 7994 |
rs142510204 | snp | A/C/G | 0.00013178 | 0.0081164 | missense, synonymous-codon | KAT6A | GRCh38.p7 | 8:41941091 | AAGGTCAGGTTTCCC[A/C/G]TCCTGGCTTGGCTGC | 7994 |
rs142564159 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:42030675 | GTTCCAGTGATACTC[A/G]TGCCTCAGCTTCTCA | 7994 |
rs142586517 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942409 | CCTGGGCCTCCTAAA[A/G]CGCTGAGATTACAGG | 7994 |
rs142588601 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:42033095 | GGCCAGGGTGGTCTC[A/G]AACTCCTGACCTCAT | 7994 |
rs142617197 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41940730 | TTAAGGTTTATAAAG[C/T]AATGCACTAGGAATT | 7994 |
rs142651705 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KAT6A | GRCh38.p7 | 8:42035156 | GAGATGTTAAAAAGT[A/G]TAAGAGAGAAGACAT | 7994 |
rs142657294 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41943069 | AATGAATGTGGAGAT[A/G]AGACCCCTGGTGAAG | 7994 |
rs142661436 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41994504 | TATATCTAGAATGTT[C/T]GTCCCAAGATCTTTC | 7994 |
rs142673548 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41991298 | ATTCATACAGTAGAA[C/T]GTTAAACAGTAATAA | 7994 |
rs142680868 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:41977920 | TTCAAGATAGTCTTA[C/T]GTGTAAAAAAAGTAA | 7994 |
rs142692669 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:42027865 | CCCTGAGGTGCAGCA[C/T]TAGGTAGTTTATGTG | 7994 |
rs142726143 | snp | C/T | 0.046775 | 0.145601 | intron-variant | KAT6A | GRCh38.p7 | 8:41959723 | CAGCACTCTGGGAGG[C/T]CAAGGTGGGCAGATC | 7994 |
rs142745698 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:42045251 | CTCTATTTTCCAACA[C/T]GTCTAAATTTAGTTA | 7994 |
rs142751773 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42046711 | TCAGCCACATGTGAT[A/G]AAGTTTCTACAGGTA | 7994 |
rs142753184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42041831 | TTTCACACTTGATAA[C/T]AGCTACATTTTCCAC | 7994 |
rs142772648 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:41953537 | AGAGTGCAATGGCGC[A/G]ATCTCAGTTCACTGC | 7994 |
rs142779931 | snp | A/G | 0.285519 | 0.247464 | intron-variant | KAT6A | GRCh38.p7 | 8:41945357 | CTCACTGAAACCTCC[A/G]CCTCCCGGGTTCAAG | 7994 |
rs142859527 | snp | C/T | 6.59174e-05 | 0.00574059 | missense | KAT6A | GRCh38.p7 | 8:41934138 | TTATCCTTTATCTTT[C/T]CCCTACTCTTCTGCA | 7994 |
rs142860503 | in-del | -/A | 0.00597247 | 0.0543191 | intron-variant | KAT6A | GRCh38.p7 | 8:41975731 | CATAAAGAAAATGAC[-/A]AGAGCCTATTAAAGC | 7994 |
rs142866892 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41973175 | TCTATTCACCACCAC[C/T]GGGTCTCTTAATATG | 7994 |
rs142903257 | snp | A/C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42042554 | AAATATAAATTCCAA[A/C/T]AAAACAAAATAATTT | 7994 |
rs142967429 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42026520 | CTAGGTTTTGTGTGA[C/T]TGTCTTGGTAGCTTT | 7994 |
rs143054165 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41965256 | ATAAAACTTTATTTA[C/T]GAACGCTAACATTTT | 7994 |
rs143054275 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:42017902 | ACTGCTGAACTCACC[A/G]CACTTAGAAGTACCT | 7994 |
rs143066567 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42011838 | AATATCTTCCCAATT[C/G]CCTGGAGCCCAAAAC | 7994 |
rs143069881 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41975474 | CTGCTGTTGGGCTCA[C/T]TTGCTCTCTTTATAA | 7994 |
rs143105254 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41980281 | TCTCAATGAACAGGA[A/G]TCAAAAGAAAAGAGT | 7994 |
rs143106751 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:42044983 | AGGAAAGAAAATAGT[C/T]AAAATACAATAAAAG | 7994 |
rs143118288 | snp | C/T | 1.6473e-05 | 0.00286988 | missense | KAT6A | GRCh38.p7 | 8:41933731 | CGTTGGGACTGCTGA[C/T]CGAACGGACTGACTG | 7994 |
rs143119525 | snp | A/C | 0.00478085 | 0.0486577 | intron-variant | KAT6A | GRCh38.p7 | 8:41977507 | TATTATTATTAGAAA[A/C]ATCTATTGCCAGGAA | 7994 |
rs143205970 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | KAT6A | GRCh38.p7 | 8:41994562 | CAGTAAGGCTTTTTT[G/T]GAACACCCCATCTAG | 7994 |
rs143207987 | snp | C/T | 1.64931e-05 | 0.00287163 | missense | KAT6A | GRCh38.p7 | 8:42048391 | ACCTTATCCTTTTCA[C/T]GTGGAAGAAGGGACA | 7994 |
rs143212958 | snp | A/G | 0.000296829 | 0.0121789 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41943750 | ATGTGATACTCACTG[A/G]TCACTACGGAAGTCC | 7994 |
rs143227770 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41937192 | TTTACTGAAGGGTCT[C/G]TCACTGCTACTGCTA | 7994 |
rs143230746 | snp | A/G | 0.00119737 | 0.0244387 | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41929526 | GTTAAAATGTACAGA[A/G]TTCTTTTGAAAGTAC | 7994 |
rs143250502 | snp | A/G | 0.0158469 | 0.0875917 | intron-variant | KAT6A | GRCh38.p7 | 8:42028458 | TTATATCCTCTTGCT[A/G]TACTGATCCCTTTAT | 7994 |
rs143273556 | snp | C/T | 0.0197687 | 0.0974348 | intron-variant | KAT6A | GRCh38.p7 | 8:41938910 | CTGAGATCATGCCGC[C/T]GCACTCCAGCCTAGG | 7994 |
rs143311944 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41990821 | ACATGGTAAAACCCC[A/G]TCTCTACTAAAAACA | 7994 |
rs143316311 | snp | A/G | 0.000153988 | 0.00877328 | missense | KAT6A | GRCh38.p7 | 8:41934810 | GTATCTGGCTCAAGA[A/G]GAGAATTCTTCACAT | 7994 |
rs143341373 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:42032202 | TGCACAACAGGCAGC[C/T]TGATGTGGCTCAAGG | 7994 |
rs143346098 | snp | A/C/G | 0.000141217 | 0.00840179 | missense | KAT6A | GRCh38.p7 | 8:41934388 | GCTCCTCTGAGACAC[A/C/G]GGGCTTCTCTTCTTC | 7994 |
rs143384432 | in-del | -/AAAAAT | 0.288127 | 0.247076 | intron-variant | KAT6A | GRCh38.p7 | 8:41995061 | ACTCCATCTCAAAAA[-/AAAAAT]AAAAATAAAAATAAA | 7994 |
rs143388721 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | KAT6A | GRCh38.p7 | 8:42045793 | CCTAGCCAACATGGT[A/G]AAACCCTGTCTCTAC | 7994 |
rs143452263 | snp | A/G | 0.000350927 | 0.0132416 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41932253 | CTTGGGCACGCCAGC[A/G]GCGTTCATGTAGCTG | 7994 |
rs143458150 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:42023161 | AGTAAAAATACAATA[A/T]ATAAGATTTTTTTAA | 7994 |
rs143485574 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42015824 | TGCAATAAGCCAAAA[C/G]AGCCAAAAAATCTGA | 7994 |
rs143527478 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | KAT6A | GRCh38.p7 | 8:42002584 | CAACAAAAACAGAAC[A/G]AAACAAAACAAAACA | 7994 |
rs143529911 | snp | A/G | | | intron-variant, upstream-variant-2KB | KAT6A, LOC105379393 | GRCh38.p7 | 8:42050328 | TCTTGTTTAATCACT[A/G]AAGTACTGAATTCTG | 7994 |
rs143531871 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41996943 | TATATTATATATTAT[A/G]TGATTCCATTTATAT | 7994 |
rs143532248 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41969492 | CAACTCCAAAATATA[C/T]CTAAATCCATCCACT | 7994 |
rs143638961 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41962414 | GTAGATGGCAACTCC[A/G]TCTTCCAACTGTGTT | 7994 |
rs143683004 | snp | A/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:41961551 | CAAGGTCAAGAGATC[A/G]AGACCATCCTGGCCA | 7994 |
rs143711390 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | KAT6A | GRCh38.p7 | 8:41944837 | TATATTAACATTAAA[G/T]GAAGTAATCTGAGTT | 7994 |
rs143730379 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42036192 | GTGGGAAGAAATACT[A/G]AATTTCTGCAGACAG | 7994 |
rs143740821 | in-del | -/TA | 0.274124 | 0.248833 | intron-variant | KAT6A | GRCh38.p7 | 8:42002016 | AACGAGAGATAAGAC[-/TA]AAATTCTCTCCTAAT | 7994 |
rs143766224 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42052720 | GCAGCTGAGAGGGTT[C/G]TTGGAGCTCACTAGA | 7994 |
rs143773919 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41965568 | TTTTTTTATTACAGC[A/G]TCAGAGAACCTGGAA | 7994 |
rs143806736 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | KAT6A | GRCh38.p7 | 8:41979728 | AATTCAGGCTGGGCG[C/T]GGTGGCTCATGCCTG | 7994 |
rs143819823 | snp | C/G | 0.000263535 | 0.011476 | missense | KAT6A | GRCh38.p7 | 8:41937366 | CGGAAGTATTCTCTA[C/G]GGAAAAGTTCATTTT | 7994 |
rs143841068 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42030393 | CTCAGAGGTTCCTCA[C/T]CCTTTCCGTGTTTAA | 7994 |
rs143849965 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41964749 | ACCCATGATATTTAA[C/T]TTATAAATTAGGCAC | 7994 |
rs143853582 | snp | C/T | 0.000134519 | 0.0082001 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41977045 | TGATTTCCTGTTGCC[C/T]CTCTTTCTGATTCGA | 7994 |
rs143887499 | snp | C/T | 4.94173e-05 | 0.00497053 | missense | KAT6A | GRCh38.p7 | 8:41934658 | CGATGGGCTCAATGA[C/T]GCATGCTTGAGTAGA | 7994 |
rs143909856 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:42024914 | AATAAATATGGGGGT[A/G]TAAGTATCCCTTTGA | 7994 |
rs143915989 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:42018884 | CAAGATCGCACCACT[A/G]CACTCCAGCCTGGCG | 7994 |
rs143968197 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42036983 | GAGGTTAAAAAGTAC[C/G]TGCTTCTTCTGTCTT | 7994 |
rs144003650 | snp | A/G | 1.64795e-05 | 0.00287045 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41940932 | GCTGCTCTCACTGAA[A/G]CCCCTGAGGACAGCC | 7994 |
rs144034651 | snp | G/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41983383 | ATCATCCTAGAATAA[G/T]AGCCATTTTTATGTT | 7994 |
rs144054857 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41987991 | CAGAAGACATTAAGT[A/G]AGAGAAACAGTAAGT | 7994 |
rs144082649 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41987746 | TGGGCCTTTACAACT[A/G]GTCCTTGTTATGACC | 7994 |
rs144084994 | snp | A/G | 0.000362402 | 0.0134562 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41932490 | ATTCATGGAATTGAC[A/G]TTATAGGCGGGAGTA | 7994 |
rs144170660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41936577 | CTGACCTGGCTCATA[C/T]ATATGAGACCTAGTT | 7994 |
rs144176444 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | KAT6A | GRCh38.p7 | 8:41947178 | TATATTTTAAGTCAC[A/C]TCTAACTAATGAAGT | 7994 |
rs144244104 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41981464 | TTAGTTTCAAGTATA[A/T]CCAATAACCAGAAAT | 7994 |
rs144334600 | snp | C/T | 0.0337553 | 0.125452 | intron-variant | KAT6A | GRCh38.p7 | 8:42046263 | ACAACAGGCCAGGCA[C/T]GGTGGCTCAAGCCTG | 7994 |
rs144371155 | snp | C/T | 0.0154538 | 0.0865337 | intron-variant | KAT6A | GRCh38.p7 | 8:42008494 | AGGCGTGCACCACCA[C/T]ACCCAGCTAAGTTTT | 7994 |
rs144380903 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41955653 | GGTGTTGCTGCATTT[A/C]TACATTTAATAACAG | 7994 |
rs144417514 | snp | A/G | 0.00393395 | 0.0441758 | missense | KAT6A | GRCh38.p7 | 8:41933268 | GGAGGCGGTGGTGGC[A/G]GCTGCTGCTGCTGGT | 7994 |
rs144417897 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:42006888 | GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAC | 7994 |
rs144500031 | snp | C/T | 0.0119091 | 0.0762411 | intron-variant | KAT6A | GRCh38.p7 | 8:42020028 | CAAATGAATCAGTGA[C/T]GCAGTGATGTTATCA | 7994 |
rs144500468 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | KAT6A | GRCh38.p7 | 8:41967758 | GCCACAATAAACATA[C/T]GTGTGCATGTGACAG | 7994 |
rs144512536 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41992330 | ACAAACTGCCATGAA[C/T]GGACAGAGAGCAGAC | 7994 |
rs144515977 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41961325 | CCGTTTGTGCATGAG[A/C]TAACATCTTCCTGCT | 7994 |
rs144566736 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | KAT6A | GRCh38.p7 | 8:42015129 | GTCAAAGTCAGAGGT[C/T]GTCTGCCAATGTTAT | 7994 |
rs144567915 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | KAT6A | GRCh38.p7 | 8:42016733 | GAGATAGAAGAAATT[C/T]TTCTCCAAGGGTAGC | 7994 |
rs144582965 | in-del | -/TC | 0.00517822 | 0.0506191 | intron-variant | KAT6A | GRCh38.p7 | 8:42010562 | CGTAGGCAAGTCTCT[-/TC]ACGATTCCAAACCCT | 7994 |
rs144589606 | snp | A/G | 3.29451e-05 | 0.00405851 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41934278 | CTCATCATCAGCGTC[A/G]TGGTCGTCATTCTGG | 7994 |
rs144590330 | snp | G/T | 0.00557542 | 0.0525036 | intron-variant | KAT6A | GRCh38.p7 | 8:41973510 | CAGGGGTGAGCCACC[G/T]TGCCCAGCCTAGAAA | 7994 |
rs144614909 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41950736 | AATGCCAACTTTAAG[A/G]GCATCCAATCCAACT | 7994 |
rs144687174 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | KAT6A | GRCh38.p7 | 8:42027059 | TTGATGCAATGTATC[A/G]CATTTATTGATTTGC | 7994 |
rs144718654 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:42022130 | AGAGTTGCTGTGATC[G/T]AAATATAATACCTAG | 7994 |
rs144720569 | snp | C/T | 7.25716e-05 | 0.00602333 | missense | KAT6A | GRCh38.p7 | 8:41933350 | TGGCAGCAGGCTGGA[C/T]GCTGCTCTGCTGCAT | 7994 |
rs144762041 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41971516 | TGAGGAAGAGGAGGC[A/G]GCTGTGGCTGGAGTA | 7994 |
rs144795826 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42018573 | TATGAATAGCTACTA[A/G]CCATCTCTGTTAAGG | 7994 |
rs144857451 | snp | A/G | | | stop-gained | KAT6A | GRCh38.p7 | 8:41977302 | TTCCAGGGCCAGTTC[A/G]AACTTTGCTGAAGGG | 7994 |
rs144895956 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42030153 | CCCTGCTGCAGCTCA[C/T]TGGGTCTCGGACAAG | 7994 |
rs144908470 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42042184 | ATATCCCTGGCCGGG[C/T]ACGGTGGCTCACGCC | 7994 |
rs144912104 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | KAT6A | GRCh38.p7 | 8:41938039 | TGTGGAATGTAGAAA[C/T]ATGGGGCTGAAATGT | 7994 |
rs144938298 | snp | A/G | 0.000132048 | 0.00812444 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933513 | GCCCATCGTGGAGTC[A/G]TAACTGCTTGGGTTC | 7994 |
rs144970208 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42038463 | GTTTATTCTATGGTT[C/T]CCATTAAGGAAGAGA | 7994 |
rs144973262 | snp | A/G | 9.85406e-05 | 0.00701859 | intron-variant | KAT6A | GRCh38.p7 | 8:41949373 | GGCAGCCTGTAAACG[A/G]TAATTAAACAAAAAA | 7994 |
rs144996910 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41992534 | TCCACTACACCATCT[C/T]TTATAAAACAGGGGT | 7994 |
rs145004468 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42022040 | TTTTAATGACTCTAC[C/T]AGCATCTACATTCTA | 7994 |
rs145079047 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42043946 | TAACCTAACAGTAGC[C/T]AGTTATGTTAGAGGA | 7994 |
rs145082081 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:41956945 | CACAACTCAAAGTAA[C/T]AACAACAGTATAGGA | 7994 |
rs145180409 | snp | C/T | 0.00011532 | 0.00759255 | missense | KAT6A | GRCh38.p7 | 8:41932429 | AACTGCTGTTCATCA[C/T]GGGCTGTGTCATTCG | 7994 |
rs145187335 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | KAT6A, LOC105379393 | GRCh38.p7 | 8:42053696 | TCCAGCACCTAGAAT[A/G]ATGTTGTACAAGTAC | 7994 |
rs145201432 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41975821 | CTCTAACAATTTCTA[C/T]TTCAAAAGCTTTCTA | 7994 |
rs145230426 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42039601 | AAAAAAGTATTGGCC[C/G]ACAAGTCCAGGATGA | 7994 |
rs145285959 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42009737 | GACCTTGTCTCTACA[A/G]AAAATTTTAAGTATT | 7994 |
rs145332537 | snp | A/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41971227 | CTTAAGGTATAATTT[A/T]AAAAAAAAAAAAAAA | 7994 |
rs145332793 | snp | G/T | 0.00755907 | 0.0610114 | intron-variant | KAT6A | GRCh38.p7 | 8:42014076 | CATATGATTTGCATG[G/T]GTTTGAAATATTATT | 7994 |
rs145411341 | snp | A/G | 1.651e-05 | 0.0028731 | synonymous-codon | KAT6A | GRCh38.p7 | 8:42048525 | GCCAATGGCACGTTT[A/G]ATAGCCAATCGTAAC | 7994 |
rs145423951 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42000379 | AACCTGGTGAAGCCT[C/T]GTCTCTACCAAAAAT | 7994 |
rs145436847 | snp | A/C/T | 0.000378815 | 0.0137576 | missense | KAT6A | GRCh38.p7 | 8:41933736 | GGACTGCTGACCGAA[A/C/T]GGACTGACTGGCTGG | 7994 |
rs145466265 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | KAT6A | GRCh38.p7 | 8:41984392 | GATGTCCACATGGCA[C/T]GGAACTGAAGCTTCT | 7994 |
rs145487556 | snp | A/G | | | utr-variant-3-prime | KAT6A | GRCh38.p7 | 8:41929786 | GCTCTATTCACACAC[A/G]CTAGAGATCTCTTTA | 7994 |
rs145560800 | snp | C/G | 0.0103295 | 0.0711199 | intron-variant | KAT6A | GRCh38.p7 | 8:42015231 | ATCCGGACTACCAAG[C/G]TGGCAGCCCTATGCT | 7994 |
rs145599135 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | KAT6A | GRCh38.p7 | 8:42041122 | ATCACTTGAACCTGG[A/G]AGGCAGAGGTTGCAG | 7994 |
rs145617464 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | KAT6A | GRCh38.p7 | 8:41994299 | CTCCAGTCCAATTGC[G/T]TCCATCTCAGATTAA | 7994 |
rs145622824 | snp | A/G | 0.000798403 | 0.0199641 | utr-variant-3-prime, intron-variant | KAT6A | GRCh38.p7 | 8:41942714 | CTGTGAAAGATGATC[A/G]TAATACATTATTATA | 7994 |
rs145651298 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42044424 | TTTAATCACAGTATC[C/T]CATGGATTCTCCTCA | 7994 |
rs145706595 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42008917 | ATTGTAATTTAAAAG[C/T]TGGTGAATAAAGCAA | 7994 |
rs145714529 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:41993303 | TCCCAGTCTTAGACC[A/G]TGCTTACTCATGACA | 7994 |
rs145724003 | snp | C/T | 1.64787e-05 | 0.00287038 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41987486 | GGCACAGGAGATGAG[C/T]TCCTCTGGCTTCTTT | 7994 |
rs145740100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42000895 | AAGTGACAAAAGTGA[C/T]ATTCAAAGTCAGGTA | 7994 |
rs145747530 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41994125 | CAAGCTTCTTTCTTA[C/T]ACCTTATTGTTCCCA | 7994 |
rs145747776 | in-del | -/CTG | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:42029199 | TTCACTGCTTTCCTC[-/CTG]CTATTTTTAGAATTC | 7994 |
rs145754397 | snp | A/G | 9.92293e-05 | 0.00704307 | missense | KAT6A | GRCh38.p7 | 8:41932620 | TGCTGGTGAGCAGCC[A/G]CAGAGGGCAGTGGCG | 7994 |
rs145777433 | snp | A/G | 0.000399281 | 0.0141238 | | | GRCh38.p7 | 8:41961638 | CACACCTGTAGTACC[A/G]GCTACTCGGGAGGCT | 7994 |
rs145778166 | snp | A/C/G/T | 0.00637159 | 0.0561118 | | | GRCh38.p7 | 8:42044350 | GTGATCCACCCCCCC[A/C/G/T]TCGGCATCCCAAAGT | 7994 |
rs145797427 | snp | A/G | 0.000643092 | 0.0179202 | missense | KAT6A | GRCh38.p7 | 8:41941348 | CTTGTTTGCTCAAAC[A/G]TGTAGAACTGACTGG | 7994 |
rs145820432 | snp | C/G | 8.25048e-05 | 0.00642228 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933840 | GTCCTCGTCAGCCTG[C/G]GTGTAACTCTGCAGG | 7994 |
rs145873968 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | KAT6A | GRCh38.p7 | 8:41953766 | GGCGTGTCCTTGGCG[A/T]ATTTCTTCTCGGTCA | 7994 |
rs145879108 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42042320 | AAATTAGCCGGGCAT[A/G]GTGGCATGCGCCTAT | 7994 |
rs145913140 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | KAT6A | GRCh38.p7 | 8:42010420 | AAATTGGGTTCAGAT[C/T]CTAGGACTTCAACTT | 7994 |
rs145928442 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | KAT6A | GRCh38.p7 | 8:41958438 | TGAAGCATAAAGACA[A/G]AAAAGAATGACATGG | 7994 |
rs146006647 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42006403 | TGGACACTCCAACTC[C/T]GTAACATCTTACGTT | 7994 |
rs146022463 | snp | A/G | | | intron-variant | KAT6A | GRCh38.p7 | 8:41945739 | GTTTAAAAATATTTC[A/G]TGTCCAAGGCCACGC | 7994 |
rs146033520 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41940781 | AACTGTAAGCTAAAA[C/T]GAGAAGGTGTAAGAT | 7994 |
rs146040001 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42032101 | TGCCTGGCTAATTTT[C/T]TGTATTTTTAGTAGA | 7994 |
rs146065216 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42036395 | GTGGGCAGATCACCT[A/G]AGGTCAGGAGTTCAA | 7994 |
rs146107524 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:42012053 | TGCAAATTAAAATCA[C/T]AATGAAATACCACTA | 7994 |
rs146164786 | snp | A/G | 0.00676609 | 0.0577691 | intron-variant | KAT6A | GRCh38.p7 | 8:41965259 | AAACTTTATTTACGA[A/G]CGCTAACATTTTTCA | 7994 |
rs146190325 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:41970591 | GCAGTGACCAAAAAG[A/G]AAGGCCTCGTTCTCA | 7994 |
rs146209687 | snp | A/G | 0.00016472 | 0.00907375 | missense | KAT6A | GRCh38.p7 | 8:41940970 | CCTCACTGTAGCGAC[A/G]GGGCAGCCTCTCACT | 7994 |
rs146227878 | snp | A/G | 1.64857e-05 | 0.00287099 | missense | KAT6A | GRCh38.p7 | 8:41974777 | TCCTGGCTCCCAAAA[A/G]GTCGCTCCTCATTTT | 7994 |
rs146228292 | snp | A/T | | | intron-variant | KAT6A | GRCh38.p7 | 8:41971224 | AAACTTAAGGTATAA[A/T]TTAAAAAAAAAAAAA | 7994 |
rs146242817 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42036567 | GCAGTGAGCAGAGAT[C/T]GCACCACTGCACTCC | 7994 |
rs146246735 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42032452 | ATTTTATTTCCCTTT[A/T]TCCTTCTTCTCTAGG | 7994 |
rs146263303 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41962840 | CTTGTACTTCCTTGA[C/T]CATGCCAAGCACAAA | 7994 |
rs146283740 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41987682 | GACAATTGTATTACT[A/C]TCCTAAATTCCAGCT | 7994 |
rs146292215 | in-del | -/A | | | intron-variant | KAT6A | GRCh38.p7 | 8:42026405 | TTCCAATCCATGAAC[-/A]GGGGATGTCTTCCCA | 7994 |
rs146403235 | snp | A/G | 0.0170251 | 0.090679 | intron-variant | KAT6A | GRCh38.p7 | 8:42007633 | TAAAACACAGCAAAG[A/G]TTTCTCCTGGGACTA | 7994 |
rs146420708 | snp | C/T | 0.0174175 | 0.0916809 | intron-variant | KAT6A | GRCh38.p7 | 8:41979265 | AGAGTGAGACTCCGT[C/T]TCAAAAAAAAAGTTT | 7994 |
rs146485011 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41936624 | AGAAATGACAACTAG[A/G]CTGCTTTAAAAGTAA | 7994 |
rs146496080 | snp | C/T | 0.00116945 | 0.0241527 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41932694 | CCCTTGCAATCTCTG[C/T]GTGTGAGGAATGCCA | 7994 |
rs146544179 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:42001023 | GAGGAAGGAGGGAAG[A/G]AAGGAGGAGGAAGGA | 7994 |
rs146585325 | snp | A/G | 0.273856 | 0.248859 | intron-variant | KAT6A | GRCh38.p7 | 8:42004877 | AGGTTGCAATGAGCC[A/G]AGATCACGCCATTGC | 7994 |
rs146617454 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41955712 | TCTTAATGACTTAAT[A/G]TTAAAGAGAAACTGC | 7994 |
rs146662151 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42022440 | GGAAAATCAGGGTTA[A/G]AACAGCCTAACAGTA | 7994 |
rs146679787 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | KAT6A | GRCh38.p7 | 8:42035322 | TGATAAATTCCATCT[A/G]AGCCATTGTGAATCT | 7994 |
rs146679799 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | KAT6A | GRCh38.p7 | 8:41980210 | TTTTTAAAGAACCTA[C/T]AAGCATATGAATATG | 7994 |
rs146687487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42028738 | TTATTATTGACAGCT[A/G]AAGACTTATCCTGTA | 7994 |
rs146725546 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41982636 | CACACTGCATACACT[A/G]CCCATTTGTTAGTCA | 7994 |
rs146782761 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42044213 | TCAAGCGATTATCCT[C/G]CCTCAGCCTACCGAG | 7994 |
rs146808187 | snp | A/C | 0.00716266 | 0.059414 | intron-variant | KAT6A | GRCh38.p7 | 8:42046535 | GATTCTGTCTCAAAA[A/C]TAAATAAATAAAAGC | 7994 |
rs146816339 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | KAT6A | GRCh38.p7 | 8:42030738 | CCTGACAAATTTTTT[G/T]TTGTTGTTGTTGTAT | 7994 |
rs146845776 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | KAT6A | GRCh38.p7 | 8:42004033 | TACTAGTAGTCAGCT[A/G]GTGAAATCACCTCAT | 7994 |
rs146850411 | snp | G/T | 0.0162398 | 0.0886349 | intron-variant | KAT6A | GRCh38.p7 | 8:42000588 | AGAAAAAAAAGTGAT[G/T]TTTTAGAAGAAGATG | 7994 |
rs146881556 | snp | A/C/T | 6.58907e-05 | 0.00573948 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933732 | GTTGGGACTGCTGAC[A/C/T]GAACGGACTGACTGG | 7994 |
rs146916621 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | KAT6A | GRCh38.p7 | 8:41984565 | TCCCAAATTCCTGAC[C/G]TACAGAAACAGTATG | 7994 |
rs146951487 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41963987 | CAGCACCCTACACAA[A/C]TGTCACCTCCTCTAC | 7994 |
rs146988900 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:42049466 | CATGTATGTAAACCA[C/T]TGGGATAAAAAAGAA | 7994 |
rs147041358 | snp | A/G | 1.6886e-05 | 0.00290564 | missense | KAT6A | GRCh38.p7 | 8:41934849 | CGCAAAAGAGATACT[A/G]GCTTTAAGATAGGAG | 7994 |
rs147056100 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41985526 | AGTCATGGTAACAAC[C/T]GTATCCATGCTTCTC | 7994 |
rs147084960 | snp | A/G | 8.01202e-05 | 0.0063288 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41934431 | AGGCTCCTTGGTTTC[A/G]GTCTCAGGACTATTG | 7994 |
rs147127020 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | KAT6A | GRCh38.p7 | 8:41938680 | GGCCAGGCGCGGTGG[C/T]TCACACCTGTAATCC | 7994 |
rs147140029 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41997082 | TTGAGATGATGGAAA[C/T]GTTCTGAATGGATGG | 7994 |
rs147169882 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:41946850 | GAAGATAGGATAATG[C/T]CAAGTCACTGCCATT | 7994 |
rs147175912 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42003247 | TCAGCTTCCTTCAGC[G/T]CTCAGAACTAGACTT | 7994 |
rs147199444 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | KAT6A | GRCh38.p7 | 8:41952438 | TCTTAATGGCAGAGT[A/C]GGTTTCGCAATGAAC | 7994 |
rs147230777 | snp | C/T | 0.00162951 | 0.0284973 | synonymous-codon | KAT6A | GRCh38.p7 | 8:41933012 | GGCACCAAAATCCCC[C/T]GGAATCCTCTCATAG | 7994 |
rs147245022 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | KAT6A | GRCh38.p7 | 8:42019385 | TGCCAGGAACATTTT[C/T]TTCCTCAGTTTCCTT | 7994 |
rs147281939 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | KAT6A | GRCh38.p7 | 8:42025810 | CCATGCTTTCGAGGT[C/T]TTAACCATAAAATCT | 7994 |