SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs1246 | snp | C/T | 0.11228 | 0.208646 | intron-variant | TAF3 | GRCh38.p7 | 10:7859920 | ATATTTAGGATGAGA[C/T]GGATTGAGAGGCATG | 83860 |
rs155415 | snp | A/G | 0.0581099 | 0.160244 | intron-variant | TAF3 | GRCh38.p7 | 10:7936996 | gccataaaaagatac[A/G]gaggaatctgaaatg | 83860 |
rs166411 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | TAF3 | GRCh38.p7 | 10:8010210 | CAATGAAGAAATGCA[C/T]CTTggctgggcatgg | 83860 |
rs174498 | snp | C/G | 0.0244538 | 0.107838 | intron-variant | TAF3 | GRCh38.p7 | 10:7969830 | GAGCTGGAATTTCCA[C/G]CCCGGTCAGTGTGGC | 83860 |
rs187821 | snp | A/G | 0.365439 | 0.221752 | intron-variant | TAF3 | GRCh38.p7 | 10:7939559 | TTTCTTCTATTTCCT[A/G]CATTGTCTCTATTTC | 83860 |
rs192346 | snp | A/G | 0.232943 | 0.249417 | intron-variant | TAF3 | GRCh38.p7 | 10:7932793 | ctactctaggggctg[A/G]ggtgggaggactgct | 83860 |
rs196527 | snp | G/T | 0.00676609 | 0.0577691 | intron-variant | TAF3 | GRCh38.p7 | 10:7994652 | TAATGTGAAAGAAAA[G/T]ATGTggctgggcgca | 83860 |
rs196528 | snp | A/G | 0.460589 | 0.13473 | intron-variant | TAF3 | GRCh38.p7 | 10:7983431 | CAGGGCAAAGAACCT[A/G]GTTGGTGTACAAAAG | 83860 |
rs197449 | snp | A/G | 0.262985 | 0.249663 | intron-variant | TAF3 | GRCh38.p7 | 10:7912061 | TATCTCCCAAACTAC[A/G]ATGACATAAAAGCAA | 83860 |
rs263414 | snp | C/T | 0.420733 | 0.18262 | intron-variant | TAF3 | GRCh38.p7 | 10:7944017 | TGGTTTTGCATTCTT[C/T]CTCTTACGCATATCA | 83860 |
rs263415 | snp | C/T | 0.420733 | 0.18262 | intron-variant | TAF3 | GRCh38.p7 | 10:7943276 | AAGCAGAACGTGATG[C/T]GTAGGAGCCAGAATC | 83860 |
rs263416 | snp | A/T | 0.180064 | 0.240019 | intron-variant | TAF3 | GRCh38.p7 | 10:7931367 | CAGGGTCAGCAGGAA[A/T]ATAAATATGGCATAG | 83860 |
rs263417 | snp | G/T | 0.420255 | 0.183066 | intron-variant | TAF3 | GRCh38.p7 | 10:7930347 | AACCTATTCATGGAT[G/T]ATTAAGAATTTGTTA | 83860 |
rs263430 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7987631 | TTCTAAAAGGCTATA[C/T]CAATTAAAATTCTCA | 83860 |
rs263431 | snp | A/T | 0.0193772 | 0.0965046 | intron-variant | TAF3 | GRCh38.p7 | 10:7987477 | AGTCACCAGTTTTCA[A/T]ACATTTAAGTTGTCA | 83860 |
rs263432 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7986880 | GCAAAACACTTAAAA[A/G]TCTGATCAGGACATA | 83860 |
rs265933 | snp | C/T | 0.418007 | 0.185132 | intron-variant | TAF3 | GRCh38.p7 | 10:7912944 | CCACAGACTGGGTGG[C/T]TTAAGCAACAGCAGT | 83860 |
rs265934 | snp | A/G | 0.417196 | 0.185864 | intron-variant | TAF3 | GRCh38.p7 | 10:7913757 | acttgtgcctcttta[A/G]ggatacagtaagagg | 83860 |
rs265935 | snp | C/G | 0.0592355 | 0.161582 | intron-variant | TAF3 | GRCh38.p7 | 10:7914371 | GCAGGTGttttcccc[C/G]tcctatttcaatcat | 83860 |
rs265937 | snp | A/C | 0.352287 | 0.228117 | intron-variant | TAF3 | GRCh38.p7 | 10:7915865 | GCACCTGTAATCCAG[A/C]TACTTGGGAGGCTGA | 83860 |
rs265940 | snp | A/C | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7958892 | ccacctcagcctccc[A/C]aagtgctggggatta | 83860 |
rs377957 | snp | C/T | 0.428182 | 0.17536 | intron-variant | TAF3 | GRCh38.p7 | 10:7956212 | GTGAGACACCGCGCC[C/T]GGCCTATTTTTTAAT | 83860 |
rs389606 | snp | A/T | 0.0150606 | 0.0854603 | intron-variant | TAF3 | GRCh38.p7 | 10:7979980 | AATTTGAATGTTACA[A/T]ATTTTCATGTGTCAT | 83860 |
rs406846 | snp | A/G | 0.179425 | 0.239831 | intron-variant | TAF3 | GRCh38.p7 | 10:7909917 | TCAGGGACCTGAGCA[A/G]TCGTGGAGCTGGGTA | 83860 |
rs407644 | snp | C/T | 0.160938 | 0.233598 | intron-variant | TAF3 | GRCh38.p7 | 10:7966448 | AACTGATAGAAACCC[C/T]GCAGTTTTGTAGGCA | 83860 |
rs415641 | snp | A/G | 0.180064 | 0.240019 | intron-variant | TAF3 | GRCh38.p7 | 10:7955209 | TGCCCCACCTCTCCC[A/G]TGCTGTCTAAGCATT | 83860 |
rs449682 | snp | A/G | 0.231189 | 0.249291 | intron-variant | TAF3 | GRCh38.p7 | 10:7963322 | ATAGAGAAAGATGGC[A/G]TTTACTGGTTAGGAA | 83860 |
rs458116 | snp | C/T | 0.428333 | 0.175206 | intron-variant | TAF3 | GRCh38.p7 | 10:7956061 | ATAATTACCTAATTA[C/T]AGTATAATTTTGGGA | 83860 |
rs464199 | snp | A/G | 0.00484259 | 0.0489678 | intron-variant | TAF3 | GRCh38.p7 | 10:7924689 | TTTCAATTTTTCTGT[A/G]ATGCTACACATATTT | 83860 |
rs466858 | snp | G/T | 0.254105 | 0.249966 | intron-variant | TAF3 | GRCh38.p7 | 10:7923590 | GTTTTGTTTTGTTTT[G/T]TTTTTTTGCTATACA | 83860 |
rs474334 | snp | A/G/T | 0.000399281 | 0.0141238 | intron-variant | TAF3 | GRCh38.p7 | 10:7953796 | CTCTGTGTTAACTAG[A/G/T]ACTAATTCATTCATT | 83860 |
rs474388 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7953780 | ACTAATTCATTCATT[C/T]GCCTATGATGTGCAC | 83860 |
rs474467 | snp | G/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7953750 | CTCTGAATCTCACTA[G/T]GGAAAGTTCTGTGTT | 83860 |
rs476901 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8008081 | aaaaGATTGTTCCCA[C/G]ACGGGCTGCAGAGGT | 83860 |
rs497482 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:7975064 | caacagaacaagact[C/T]tgtctcaaaaaaaaa | 83860 |
rs500915 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8007842 | TTTATTataaaaagc[A/G]ctatttattgaggac | 83860 |
rs500948 | snp | A/G | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:8007828 | cactatttattgagg[A/G]cctataagaagttag | 83860 |
rs501874 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007722 | cttttgtagatgagg[A/G]aactgaagatcagca | 83860 |
rs502031 | snp | C/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007660 | CTTTTGAACCAAAGT[C/G]TACTTGATTCCAAAG | 83860 |
rs531053 | snp | C/T | | | intron-variant | TAF3 | GRCh38.p7 | 10:8007804 | AAGTTAGAGGTTATA[C/T]TAGGCACTTTACAAA | 83860 |
rs768165 | snp | A/T | 0.0707826 | 0.174302 | intron-variant | TAF3 | GRCh38.p7 | 10:8005671 | TGATGGAACCAAAGC[A/T]AAAGGGAAAAGCAGG | 83860 |
rs768166 | snp | A/C | 0.364401 | 0.222289 | intron-variant | TAF3 | GRCh38.p7 | 10:8005587 | TTAGGCAAGTCTGAT[A/C]TTTGGTTATGATGAA | 83860 |
rs768167 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | TAF3 | GRCh38.p7 | 10:8005311 | TCTTTAAAAAAAATA[A/C]GCAGCACATAATCAA | 83860 |
rs794551 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830689 | gggtttcaccatgtt[A/G]gccaggctggtctgg | 83860 |
rs794552 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830696 | accatgttggccagg[A/C]tggtctggaactcct | 83860 |
rs794553 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830744 | cagcctcggcctccc[A/C]aagtgctgggattcc | 83860 |
rs794555 | snp | A/G | | | intron-variant | TAF3 | GRCh38.p7 | 10:7915519 | agtagctgggactac[A/G]ggcgcctgccaccac | 83860 |
rs794556 | snp | C/T | 0.493293 | 0.0575177 | intron-variant | TAF3 | GRCh38.p7 | 10:7915373 | acaggcgtgagccac[C/T]gcgcccggccCATGA | 83860 |
rs797015 | snp | A/C | | | intron-variant | TAF3 | GRCh38.p7 | 10:7830650 | caccacgcccagcta[A/C]tttttgtatttttag | 83860 |
rs811195 | snp | C/T | 0 | 0 | intron-variant | TAF3 | GRCh38.p7 | 10:7915367 | atgagccaccgcgcc[C/T]ggccCAAAAGTGATC | 83860 |
rs877345 | snp | A/C | 0.0310518 | 0.120672 | intron-variant | TAF3 | GRCh38.p7 | 10:8011813 | ATCTACTGGAAAACC[A/C]GAACTTTTAGAGCTA | 83860 |
rs914607 | snp | A/T | 0.178465 | 0.239547 | intron-variant | TAF3 | GRCh38.p7 | 10:7934459 | agactctgtctcaaa[A/T]aaataaataaataaa | 83860 |
rs914608 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | TAF3 | GRCh38.p7 | 10:7934216 | ATTTTCTTAATAGAT[C/T]GCTCATCCATACATT | 83860 |
rs951096 | snp | A/G | 0.441021 | 0.161279 | intron-variant | TAF3 | GRCh38.p7 | 10:7930647 | TACCTGAGTACAGTC[A/G]TCAATATTTTTAAGC | 83860 |
rs975101 | snp | A/G | 0.347253 | 0.230308 | intron-variant | TAF3 | GRCh38.p7 | 10:7878671 | TGAATTAATTATAGT[A/G]CATCTAGAGAGGGAA | 83860 |
rs1018699 | snp | C/T | 0.184203 | 0.241186 | intron-variant | TAF3 | GRCh38.p7 | 10:7882044 | CAACTCTGCTCAGTT[C/T]AGTTTTGAACTCACT | 83860 |
rs1018700 | snp | A/G | 0.480144 | 0.097642 | intron-variant | TAF3 | GRCh38.p7 | 10:7880109 | tgagattacaggtgc[A/G]tgccaccaaggccag | 83860 |
rs1018701 | snp | C/T | 0.332106 | 0.236133 | intron-variant | TAF3 | GRCh38.p7 | 10:7878227 | GCATTTGCTATTTTA[C/T]ATTACTTTCTTTAAA | 83860 |
rs1041541 | snp | A/C | 0.36021 | 0.224397 | intron-variant | TAF3 | GRCh38.p7 | 10:7880306 | AATGAAGGCACTCTG[A/C]TAAATCAAAGTTATT | 83860 |
rs1057735 | snp | A/G | 1.66081e-05 | 0.00288163 | missense | TAF3 | GRCh38.p7 | 10:7964891 | GGAACCTCAAGTTCC[A/G]ATAACTCATGGACAA | 83860 |
rs1064134 | snp | A/G | 0.482905 | 0.0908579 | intron-variant | TAF3 | GRCh38.p7 | 10:7856796 | tatctaaaggactcc[A/G]aagccaacttaAAGA | 83860 |
rs1244229 | snp | C/T | 0.399722 | 0.200208 | missense | TAF3 | GRCh38.p7 | 10:7965597 | AGGAGAAAGAGAAGG[C/T]GAAGGAGAAAGAAAA | 83860 |
rs1244440 | snp | A/G | 0.431621 | 0.171796 | intron-variant | TAF3 | GRCh38.p7 | 10:7890600 | TTAAATTCTAATCAG[A/G]CAATCAACACTCACA | 83860 |
rs1244441 | snp | A/G | 0.429388 | 0.174127 | intron-variant | TAF3 | GRCh38.p7 | 10:7890401 | CTACTATGATGGAAC[A/G]TAGACTACAAACACA | 83860 |
rs1244455 | snp | G/T | 0.13446 | 0.221699 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817005 | agttgaagtgtacac[G/T]tgagtctatgatttt | 83860 |
rs1244456 | snp | C/T | 0.4628 | 0.13121 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817144 | ACAGATTTGtgaaat[C/T]caaggcgcaagagag | 83860 |
rs1244457 | snp | C/T | 0.299664 | 0.245017 | upstream-variant-2KB, intron-variant | TAF3, LOC105376392 | GRCh38.p7 | 10:7817171 | AGAGTTTCAATGTTA[C/T]Agaagcgttcaacat | 83860 |
rs1244458 | snp | A/C | 0.183568 | 0.241012 | intron-variant | TAF3 | GRCh38.p7 | 10:7887784 | AAAGGATTTTAATAA[A/C]CCAAAAGGTATAACC | 83860 |
rs1244459 | snp | A/G | 0.231189 | 0.249291 | intron-variant | TAF3 | GRCh38.p7 | 10:7886277 | TGGTAAACATTAGGG[A/G]GCGGCTGGTTATGTC | 83860 |
rs1244460 | snp | A/C | 0.184838 | 0.241358 | intron-variant | TAF3 | GRCh38.p7 | 10:7881848 | CTTTTCTTTTTAATG[A/C]GTTAACTAGGGCACA | 83860 |
rs1244461 | snp | C/T | 0.421368 | 0.182025 | intron-variant | TAF3 | GRCh38.p7 | 10:7881545 | TACGTTCCAGCTTCA[C/T]TGCTAAATTTTATAC | 83860 |
rs1244462 | snp | A/G | 0.455144 | 0.142885 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819059 | AGTCATCCTTCGGGT[A/G]CCTCTTCCTTATCCG | 83860 |
rs1244463 | snp | A/G | 0.089084 | 0.191327 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7819580 | GCTACAGTACTTATG[A/G]GTTTTAAATGAATGT | 83860 |
rs1244464 | snp | C/T | 0.427423 | 0.176128 | intron-variant, upstream-variant-2KB | TAF3, LOC105376392 | GRCh38.p7 | 10:7820036 | CTAGCATTTTGCTTA[C/T]CTTTTGCCAGCCTGC | 83860 |
rs1244465 | snp | C/T | 0.464735 | 0.128019 | intron-variant | TAF3 | GRCh38.p7 | 10:7822944 | ATTACATTTGAAAAT[C/T]TATAGATAAATTATC | 83860 |
rs1244466 | snp | C/T | 0.381697 | 0.212499 | intron-variant | TAF3 | GRCh38.p7 | 10:7823012 | cagctactcagaagg[C/T]gaaggtaggaggatg | 83860 |
rs1244467 | snp | A/G | 0.464841 | 0.127841 | intron-variant | TAF3 | GRCh38.p7 | 10:7823120 | cctgtctcaaaaaac[A/G]aacaaaaaCCAAACT | 83860 |
rs1244468 | snp | C/T | 0.0887219 | 0.191022 | intron-variant | TAF3 | GRCh38.p7 | 10:7823733 | tccgcctcctgggtt[C/T]gagcagttctcctgc | 83860 |
rs1244469 | snp | C/T | 0.300421 | 0.244863 | intron-variant | TAF3 | GRCh38.p7 | 10:7823922 | aggcgtgagccatcg[C/T]gcccagctAAGATGC | 83860 |
rs1244470 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | TAF3 | GRCh38.p7 | 10:7824244 | CATATTTACTTACta[C/T]tttttcttaatattt | 83860 |
rs1244471 | snp | C/T | 0.489588 | 0.0713983 | intron-variant | TAF3 | GRCh38.p7 | 10:7824594 | TTCATATGTTAGTGA[C/T]TATTTTAATGGATTT | 83860 |
rs1244472 | snp | A/T | 0.464735 | 0.128019 | intron-variant | TAF3 | GRCh38.p7 | 10:7824613 | TTTAATGGATTTTTA[A/T]TCCTCTTAGCTTTCC | 83860 |
rs1244473 | snp | C/G | 0.0644693 | 0.167566 | intron-variant | TAF3 | GRCh38.p7 | 10:7825188 | ATATTTAAGTAATTT[C/G]TGGTCTCTAACACAA | 83860 |
rs1244474 | snp | A/G | 0.464735 | 0.128019 | intron-variant | TAF3 | GRCh38.p7 | 10:7825414 | atacattgttattca[A/G]ccatcatccccatcc | 83860 |
rs1244475 | snp | G/T | 0.468249 | 0.121932 | intron-variant | TAF3 | GRCh38.p7 | 10:7825583 | ttataaatggacttg[G/T]acattatttgtcttt | 83860 |
rs1244476 | snp | A/C | 0.316726 | 0.240931 | intron-variant | TAF3 | GRCh38.p7 | 10:7827785 | actctgtctcaaaaa[A/C]aaaaaaaaaaacaaa | 83860 |
rs1244477 | snp | A/C | 0.474091 | 0.11083 | intron-variant | TAF3 | GRCh38.p7 | 10:7827791 | tctcaaaaaaaaaaa[A/C]aaaaacaaaaacaaa | 83860 |
rs1244478 | snp | A/G | 0.433818 | 0.169443 | intron-variant | TAF3 | GRCh38.p7 | 10:7827851 | gtagtcccagctatc[A/G]gagtctgtggtggga | 83860 |
rs1244479 | snp | A/G | 0.498774 | 0.02473 | intron-variant | TAF3 | GRCh38.p7 | 10:7828181 | gaggctgtagtgcgc[A/G]atgattgagcctgtg | 83860 |
rs1244480 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | TAF3 | GRCh38.p7 | 10:7828361 | AGCTGTGTGATTATC[C/T]GCAGTGTGAAGATGA | 83860 |
rs1244481 | snp | C/G | 0.299916 | 0.244966 | intron-variant | TAF3 | GRCh38.p7 | 10:7849663 | aaaGTTCGCATGAAC[C/G]CCCCCAATAGTTGTT | 83860 |
rs1244482 | snp | A/C | 0.300169 | 0.244914 | intron-variant | TAF3 | GRCh38.p7 | 10:7849544 | CCACAACTATTATGC[A/C]CATTTAAAACACAAT | 83860 |
rs1244483 | snp | A/C | 0.0991586 | 0.199366 | intron-variant | TAF3 | GRCh38.p7 | 10:7849487 | CATACAATGCTTATG[A/C]AACATAAATTCACAC | 83860 |
rs1244484 | snp | G/T | 0.0908922 | 0.192833 | intron-variant | TAF3 | GRCh38.p7 | 10:7849327 | TCACTTGTAGTAATA[G/T]AATCTAAAGACAAAA | 83860 |
rs1244485 | snp | C/T | 0.309648 | 0.24278 | intron-variant | TAF3 | GRCh38.p7 | 10:7847904 | tgggtgcctgtagtc[C/T]cagctactcgggagg | 83860 |
rs1244486 | snp | A/C | 0.300673 | 0.244811 | intron-variant | TAF3 | GRCh38.p7 | 10:7846704 | CTCATCATGTCTTAG[A/C]TTTATAGGAGGTCCA | 83860 |
rs1244487 | snp | A/G | 0.300673 | 0.244811 | intron-variant | TAF3 | GRCh38.p7 | 10:7846597 | AGCCTCTAGGAAAGA[A/G]TAAAAATCATGAAAT | 83860 |
rs1244488 | snp | A/G | 0.378568 | 0.214407 | intron-variant | TAF3 | GRCh38.p7 | 10:7846404 | AAAATCACAAATGCA[A/G]ATAAAGCAACTATCA | 83860 |
rs1244489 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | TAF3 | GRCh38.p7 | 10:7845998 | gcactccagcctggg[C/T]gacaggcgagacatt | 83860 |
rs1244490 | snp | C/T | 0.0923359 | 0.194016 | intron-variant | TAF3 | GRCh38.p7 | 10:7845878 | ATCTGTTGCCTTCAA[C/T]GCATTTGAAAAGAAA | 83860 |