SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs954347 | snp | G/T | 0.103082 | 0.202275 | intron-variant | TAF5 | GRCh38.p7 | 10:103380708 | caacctctgcctccc[G/T]ggttcaaacgattct | 6877 |
rs1052182 | snp | A/G | | | missense | TAF5 | GRCh38.p7 | 10:103368365 | GGGCTGCTGGAGGAG[A/G]CAGTGGCGGGCGCCG | 6877 |
rs1052183 | snp | G/T | 0 | 0 | missense | TAF5 | GRCh38.p7 | 10:103378337 | GACCATGTTGGATTT[G/T]CGAACAAGTAAATTT | 6877 |
rs1052184 | snp | C/T | 0 | 0 | missense | TAF5 | GRCh38.p7 | 10:103379969 | CGAGTGCGCCTTGGG[C/T]CGGACTGCTTACCCT | 6877 |
rs2176448 | snp | A/T | 0.438666 | 0.164028 | intron-variant | TAF5 | GRCh38.p7 | 10:103381277 | TCCATCTCAAAAAAA[A/T]AATAATAATAAAATA | 6877 |
rs2945129 | snp | A/G | | | intron-variant | TAF5 | GRCh38.p7 | 10:103383670 | aatcgcttgaaccca[A/G]gaagcggaagttgcg | 6877 |
rs3004632 | snp | A/G | | | intron-variant | TAF5 | GRCh38.p7 | 10:103383809 | gggcagatcacctga[A/G]gttgagagttcaaga | 6877 |
rs4918008 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | TAF5 | GRCh38.p7 | 10:103368914 | CGTACTTTAAGTACT[A/G]TAAGTACTTTATTTT | 6877 |
rs4918009 | snp | C/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103369355 | agttgaatttttttt[C/T]tttttctttttttct | 6877 |
rs4918010 | snp | C/T | 0 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103369362 | ttttttttctttttc[C/T]ttttttctttttttg | 6877 |
rs4918011 | snp | A/C | 0.135484 | 0.22223 | intron-variant | TAF5 | GRCh38.p7 | 10:103370695 | TGCCTCTGTGTATGT[A/C]CCTGAAACCTGAGCC | 6877 |
rs4918012 | snp | A/G | 0.489893 | 0.0703642 | intron-variant | TAF5 | GRCh38.p7 | 10:103371055 | AGACCAGCTTGGCCA[A/G]CATGGTGAAACCCCA | 6877 |
rs7069667 | snp | A/G | 0.0916144 | 0.193427 | intron-variant | TAF5 | GRCh38.p7 | 10:103385229 | TTAATATAGTCAAAT[A/G]TATATAAAATATTAA | 6877 |
rs7071418 | snp | A/G | 0.103082 | 0.202275 | intron-variant | TAF5 | GRCh38.p7 | 10:103380190 | ctggagtgcagtggc[A/G]cgatctcagctcact | 6877 |
rs7099480 | snp | A/G | 0.243347 | 0.249911 | intron-variant | TAF5 | GRCh38.p7 | 10:103384500 | GCAGGGTGTGGTGGC[A/G]CCCACCTGTAATCCT | 6877 |
rs7893168 | snp | G/T | 0.0244538 | 0.107838 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103366689 | gtctcgtactgtcgc[G/T]caggctggagtgcag | 6877 |
rs7894768 | snp | C/T | 0.495174 | 0.0488838 | intron-variant | TAF5 | GRCh38.p7 | 10:103375855 | ctgaggtcaggagtt[C/T]gagaccagcctggcc | 6877 |
rs7905968 | snp | C/T | 0.495135 | 0.0490805 | intron-variant | TAF5 | GRCh38.p7 | 10:103375562 | TATGAGAGCTCAGAA[C/T]AGAGGTAGGGACTAG | 6877 |
rs7913980 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | TAF5 | GRCh38.p7 | 10:103376769 | caaaaattgagccgg[G/T]catggtggctcatgc | 6877 |
rs9731444 | snp | A/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103382650 | AGGtttttttttttt[A/T]attttaaattttttt | 6877 |
rs10883856 | snp | G/T | 0.00597247 | 0.0543191 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103366171 | CCACAGAGTTACAAG[G/T]TTCCAATGAGATAAA | 6877 |
rs10883857 | snp | G/T | 0.490836 | 0.0670685 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103367830 | CCTTTCTTTCGCTCG[G/T]TTTTGAAAGTTGCTC | 6877 |
rs10883858 | snp | A/G | 0.498108 | 0.0306996 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103367951 | CCATGTGGCGAAAAT[A/G]CAATCACGCTTGACG | 6877 |
rs10883859 | snp | G/T | 0.455962 | 0.141702 | missense | TAF5 | GRCh38.p7 | 10:103368377 | GAGGCAGTGGCGGGC[G/T]CCGGAGCCCCGGGAG | 6877 |
rs10883861 | snp | C/T | 0.197393 | 0.244402 | intron-variant | TAF5 | GRCh38.p7 | 10:103369908 | GTGTGATGCTGATTG[C/T]Cattatttttttagt | 6877 |
rs11191666 | snp | A/G | 0.490782 | 0.0672626 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103367521 | ACTGAGCCATCTGCG[A/G]GGTGGGGATAATATT | 6877 |
rs11191667 | snp | A/G | 0.422944 | 0.180528 | intron-variant | TAF5 | GRCh38.p7 | 10:103369141 | CTACTGCCACGGCCG[A/G]CTAATTTTTGTATTT | 6877 |
rs11191668 | snp | A/G | | | intron-variant | TAF5 | GRCh38.p7 | 10:103370147 | tgaggcaggagaatc[A/G]cttgaccccgggagg | 6877 |
rs11191669 | snp | C/T | 0 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103373646 | TACGTAGTGTGTGTG[C/T]GTGCGTGCATATGTT | 6877 |
rs11191670 | snp | A/T | 0.0383715 | 0.133092 | intron-variant | TAF5 | GRCh38.p7 | 10:103373704 | GACTGCAACTTAAAA[A/T]GTACGTTGTGAAGGA | 6877 |
rs11191671 | snp | C/G | 0 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103378134 | GGATTATTTAGACTA[C/G]TACATTGAAAATATT | 6877 |
rs11191672 | snp | C/T | 0.490287 | 0.0690083 | intron-variant | TAF5 | GRCh38.p7 | 10:103379204 | cagaatgtggctttc[C/T]tctttgtgctcacaa | 6877 |
rs11191673 | snp | A/G | 0.132751 | 0.2208 | intron-variant | TAF5 | GRCh38.p7 | 10:103382422 | tagagatagggtttc[A/G]ccatgttggccaggc | 6877 |
rs11191674 | snp | A/G | 0.0058139 | 0.0536018 | intron-variant, utr-variant-3-prime | USMG5, TAF5 | GRCh38.p7 | 10:103388572 | CAAGATTCAAATTCA[A/G]AAATATACTATCATC | 6877 |
rs11427664 | in-del | -/T | 0.0926964 | 0.194308 | intron-variant | TAF5 | GRCh38.p7 | 10:103369346 | AGTTGAATTTTTTTT[-/T]CTTTTTCTTTTTTTC | 6877 |
rs11438882 | in-del | -/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103383595 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTTTCGC | 6877 |
rs11596937 | snp | C/T | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103375033 | ctgaggctggagaat[C/T]gcttgaacctgggag | 6877 |
rs12244173 | snp | C/G | | | intron-variant | TAF5 | GRCh38.p7 | 10:103386739 | cgccatctcggctca[C/G]tgcaacctctacctc | 6877 |
rs12268075 | snp | C/T | 0.0279526 | 0.114869 | intron-variant | TAF5 | GRCh38.p7 | 10:103378806 | gggattagaggcaca[C/T]gccaccaacctggct | 6877 |
rs12414443 | snp | A/G | 0.489893 | 0.0703642 | intron-variant | TAF5 | GRCh38.p7 | 10:103386585 | cacgcctatagtccc[A/G]gctactggggaggct | 6877 |
rs12767489 | snp | A/G | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103385951 | aaaaaaaaaaaaaaa[A/G]gaaaAGAAATTGGGG | 6877 |
rs12767811 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | TAF5 | GRCh38.p7 | 10:103385913 | ctaggggacaagagc[A/G]agacttcatctcaaa | 6877 |
rs12776544 | snp | C/T | 0.0360663 | 0.129354 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103366271 | ttttttttcctgaga[C/T]ggagttttgttcttg | 6877 |
rs12776876 | snp | A/G | | | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103366269 | ttttttttttcctga[A/G]acggagttttgttct | 6877 |
rs12777991 | snp | C/T | | | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103366263 | ttttttttttttttt[C/T]cctgagacggagttt | 6877 |
rs12778226 | snp | C/G | | | intron-variant | TAF5 | GRCh38.p7 | 10:103375321 | AGGTGAAGAGAAGTA[C/G]ACAAAGTCATGAGAC | 6877 |
rs12781182 | snp | A/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103370242 | gtctcaaaaaaaaaa[A/T]TTTTTTTTTACATTA | 6877 |
rs34045284 | snp | A/G | 0.000236183 | 0.0108644 | synonymous-codon | TAF5 | GRCh38.p7 | 10:103379658 | TCCCTCTTCATCCTC[A/G]TCATCCAAAGGTACC | 6877 |
rs34262432 | in-del | -/T | 0.496999 | 0.0386216 | intron-variant | TAF5 | GRCh38.p7 | 10:103368982 | ATTTTTTTTTTTTTT[-/T]GAGACGGAAACTTGC | 6877 |
rs34455919 | in-del | -/T | | | intron-variant, downstream-variant-500B | USMG5, TAF5 | GRCh38.p7 | 10:103389502 | TAATTTTGTATTTTT[-/T]AGTAGAGACAGGGTT | 6877 |
rs34575405 | in-del | -/G | | | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103367239 | GCACTCCAGCCTGGG[-/G]CGACAGAGCGACACT | 6877 |
rs34851825 | in-del | -/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103386681 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCGC | 6877 |
rs35298469 | in-del | -/C | | | intron-variant | TAF5 | GRCh38.p7 | 10:103387774 | TGCAATACTAAGTCC[-/C]TTATGTTTTAGGTTT | 6877 |
rs35591196 | in-del | -/A | | | intron-variant | TAF5 | GRCh38.p7 | 10:103377529 | TATTTTCTTAGGAAA[-/A]TTAAGCGTTGTAAAA | 6877 |
rs35965152 | snp | A/G | 0.0032578 | 0.0402279 | synonymous-codon | TAF5 | GRCh38.p7 | 10:103387310 | GTTACCATTCAGGAC[A/G]TCCCAGAGCCGCACA | 6877 |
rs41303823 | snp | A/C | 0.0402882 | 0.136092 | intron-variant | TAF5 | GRCh38.p7 | 10:103382072 | AATGAGTGAGTATTA[A/C]GCTAAAAAACTTAAA | 6877 |
rs45589131 | snp | A/G | 3.31543e-05 | 0.00407137 | intron-variant | TAF5 | GRCh38.p7 | 10:103387983 | ATGGATGCAACTAAT[A/G]GTTTCCTTTGACTTC | 6877 |
rs55719019 | in-del | -/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103383966 | CCCTTTTTTTTTTTT[-/T]AATTATTTTTATTTG | 6877 |
rs57707166 | snp | A/C | 0.0263992 | 0.111815 | intron-variant, utr-variant-3-prime | USMG5, TAF5 | GRCh38.p7 | 10:103388893 | CATACAACCTAGTAC[A/C]CTTGAAGTCAGACAG | 6877 |
rs58575527 | in-del | -/AACT | 0.172351 | 0.237636 | intron-variant | TAF5 | GRCh38.p7 | 10:103387069 | GGGGGGCCCACTCAG[-/AACT]AACTTTTTATGTGGA | 6877 |
rs59387508 | snp | A/G | 0.031825 | 0.122064 | intron-variant | TAF5 | GRCh38.p7 | 10:103370963 | ATGTGATTGAAGGCC[A/G]GGCTCGGTGGCTCAC | 6877 |
rs59744322 | snp | G/T | 0.490836 | 0.0670685 | intron-variant | TAF5 | GRCh38.p7 | 10:103386935 | CCCAAAGTGCTAGAA[G/T]TGTAAGCGTGAGCCC | 6877 |
rs61869839 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | TAF5 | GRCh38.p7 | 10:103372707 | TTGAGACTAGCCTGG[C/T]CAACATAGTGAAACC | 6877 |
rs61869857 | snp | A/G | 0.48995 | 0.0701706 | intron-variant | TAF5 | GRCh38.p7 | 10:103372709 | GAGACTAGCCTGGTC[A/G]ACATAGTGAAACCCC | 6877 |
rs61869858 | snp | C/T | 0.0368353 | 0.130617 | intron-variant | TAF5 | GRCh38.p7 | 10:103383681 | CCTCCTGGGTTCAAG[C/T]GATTCTCCTGGCTCA | 6877 |
rs61869859 | snp | C/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103383952 | TTAGCTTTAGTATTT[C/T]CCTTTTTTTTTTTTA | 6877 |
rs61871160 | snp | C/T | 0.48978 | 0.0707512 | intron-variant | TAF5 | GRCh38.p7 | 10:103384531 | GGCTACTTGGGAGGC[C/T]GAGGCAGGAAAGTCA | 6877 |
rs61871161 | snp | A/G | | | intron-variant | TAF5 | GRCh38.p7 | 10:103385851 | AATCATTTGAACCTG[A/G]GAGGCGGAGGTTGCA | 6877 |
rs61871162 | snp | A/G | 0.490943 | 0.0666801 | intron-variant | TAF5 | GRCh38.p7 | 10:103385900 | ATTGCACTCCAGCCT[A/G]GGGGACAAGAGCGAG | 6877 |
rs72847518 | snp | A/C | 0.0310518 | 0.120672 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103367434 | GTTTTTGAGTTAAAT[A/C]CGTGGATTCGAATGT | 6877 |
rs73316878 | snp | A/C | 0.0248432 | 0.108648 | intron-variant, utr-variant-3-prime | USMG5, TAF5 | GRCh38.p7 | 10:103388757 | TCTTAGATCTAGAGG[A/C]AGTACAGCCACCCAC | 6877 |
rs74582980 | snp | G/T | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103380632 | ATTTTTTTTTTTTTT[G/T]GAGACAGAGTTTTGT | 6877 |
rs74941962 | snp | G/T | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103383596 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTTTCGCT | 6877 |
rs75303881 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103367329 | TTTACAAAAGTAAAA[A/T]TGACAAAAAAAAAAA | 6877 |
rs75351305 | snp | A/G | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103372914 | AAGAAAAAAAAAAAA[A/G]ACTACGTGGGCCAGG | 6877 |
rs75788505 | snp | A/C | 0.00318978 | 0.0398085 | intron-variant | TAF5 | GRCh38.p7 | 10:103384690 | CAAGGTTTCATCATT[A/C]CGAAACTTTGAGAAT | 6877 |
rs76118965 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | TAF5 | GRCh38.p7 | 10:103373929 | GGCTGAAAGATGGCC[A/G]GGGTAGCTGGAGCAG | 6877 |
rs76231647 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | TAF5 | GRCh38.p7 | 10:103381406 | CAAGTAGATGGGATT[A/G]CAGGTGCCCACCACC | 6877 |
rs76652215 | snp | A/C | 0.0248432 | 0.108648 | intron-variant | TAF5 | GRCh38.p7 | 10:103371255 | CTTTACAAAAAAAAA[A/C]AAAAAGAGAGAGGAA | 6877 |
rs76991454 | snp | A/C | 0.0178098 | 0.0926698 | intron-variant | TAF5 | GRCh38.p7 | 10:103383060 | ATCTGTTCTGAACGT[A/C]ATTTTCTTCTCTTAC | 6877 |
rs77148984 | snp | G/T | 0 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103371943 | ACTCCTTGTTATTGT[G/T]TTTTTTTTTTTTGAG | 6877 |
rs77199010 | snp | A/T | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103375036 | AGGCTGGAGAATCGC[A/T]TGAACCTGGGAGATA | 6877 |
rs77202190 | snp | A/G | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103376581 | AGCCAAGTGCTTTTG[A/G]AAAAAAAAAAAATAA | 6877 |
rs77467282 | snp | A/T | 0.0322114 | 0.122752 | intron-variant | TAF5 | GRCh38.p7 | 10:103383966 | TCCCTTTTTTTTTTT[A/T]AATTATTTTTATTTG | 6877 |
rs78049310 | snp | A/C | 0.5 | 0 | upstream-variant-2KB | TAF5 | GRCh38.p7 | 10:103367333 | CAAAAGTAAAAATGA[A/C]AAAAAAAAAAAAAAA | 6877 |
rs78322155 | snp | A/G | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103375519 | CTTTGACTCATTTAA[A/G]AAATGTCAAGTTGAT | 6877 |
rs78466037 | snp | G/T | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103380633 | TTTTTTTTTTTTTTT[G/T]AGACAGAGTTTTGTG | 6877 |
rs78702046 | snp | C/T | 0.00231758 | 0.033962 | synonymous-codon | TAF5 | GRCh38.p7 | 10:103368325 | CAAACTCCGCGAGGC[C/T]GAAGAGGCGCTGCGC | 6877 |
rs78748561 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | TAF5 | GRCh38.p7 | 10:103374631 | GATATTTGGGGAGAG[C/T]GAAGCCTTTTTGCTA | 6877 |
rs78781676 | snp | A/G | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103376580 | TAGCCAAGTGCTTTT[A/G]AAAAAAAAAAAAATA | 6877 |
rs78970616 | snp | A/G | 0.5 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103386278 | ACCCCGTCTCTACTG[A/G]AAAAAAAAACAAAAA | 6877 |
rs79594876 | snp | A/G | 0 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103372913 | AAAGAAAAAAAAAAA[A/G]GACTACGTGGGCCAG | 6877 |
rs80283300 | snp | A/T | 0 | 0 | intron-variant | TAF5 | GRCh38.p7 | 10:103370232 | ACGAGACTCTGTCTC[A/T]AAAAAAAAATTTTTT | 6877 |
rs111344864 | snp | G/T | | | intron-variant | TAF5 | GRCh38.p7 | 10:103378735 | TGATCTCAGCTCACT[G/T]CAACCTCCACCTCCT | 6877 |
rs111734917 | snp | A/C | 0.00795532 | 0.062565 | intron-variant | TAF5 | GRCh38.p7 | 10:103384554 | GAAAGTCACTTGAAC[A/C]TGGGAGGCAGAGGTT | 6877 |
rs111823138 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | TAF5 | GRCh38.p7 | 10:103381025 | TGCAATTTTGGCTCA[C/T]TGCAACCTCCGCCTC | 6877 |
rs112312319 | snp | C/T | 0.00268239 | 0.036524 | synonymous-codon | TAF5 | GRCh38.p7 | 10:103388172 | AGTTGTACACCTTCA[C/T]TTTACTCGAAGAAAC | 6877 |
rs112397177 | snp | G/T | 0.0126979 | 0.078662 | intron-variant | TAF5 | GRCh38.p7 | 10:103375065 | TAGAGGTTGCAGTGA[G/T]CTGAGATTGCATCTC | 6877 |
rs112488541 | in-del | -/G | 0.00517822 | 0.0506191 | intron-variant | TAF5 | GRCh38.p7 | 10:103371602 | TTTCTGTTTTGAAGT[-/G]GTGGTTATGGAAATT | 6877 |
rs112715180 | snp | A/G | 0.5 | 0 | missense | TAF5 | GRCh38.p7 | 10:103381742 | ACTGCAGTGGATGTC[A/G]CTGATGATTCTAGTC | 6877 |