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 |