SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13065 | snp | A/G | 0.499712 | 0.0122623 | synonymous-codon | WDR25 | GRCh38.p7 | 14:100529975 | GGGCAGCACGGGGTG[A/G]TAGGTGGTGCCGACA | 79446 |
rs13492 | snp | C/G | 0 | 0 | utr-variant-3-prime | WDR25 | GRCh38.p7 | 14:100530259 | CACACATTTATTGGG[C/G]ATCGCCGGCTGCCCG | 79446 |
rs736319 | snp | A/G | 0.0966517 | 0.197444 | intron-variant | WDR25 | GRCh38.p7 | 14:100422943 | ATTGAAGTGGCGAGC[A/G]TCCCACAGAGTTTAT | 79446 |
rs941924 | snp | C/T | 0.471768 | 0.115407 | intron-variant | WDR25 | GRCh38.p7 | 14:100426412 | TCAGAGAACTTGGAA[C/T]ACAAATTTATAACTT | 79446 |
rs941925 | snp | A/G | 0.466412 | 0.125164 | intron-variant | WDR25 | GRCh38.p7 | 14:100424453 | CCTGGGGTCAGTGGC[A/G]GGTCCCCAGTAGCAA | 79446 |
rs941926 | snp | C/T | 0.422315 | 0.181128 | upstream-variant-2KB, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100374613 | TGCAGAATCAGCGTG[C/T]CCTGATCTCTGTGAG | 79446 |
rs941927 | snp | A/G | 0.422158 | 0.181278 | upstream-variant-2KB, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100374476 | TTATGCTCCTCCACC[A/G]CAGTGGAAACTTTCA | 79446 |
rs999045 | snp | C/T | 0.464096 | 0.129085 | intron-variant | WDR25 | GRCh38.p7 | 14:100402890 | TGCTGGCTGGCTGCA[C/T]GGGTCTCATCCCTAT | 79446 |
rs1128647 | snp | C/T | 0 | 0 | utr-variant-3-prime | WDR25 | GRCh38.p7 | 14:100530157 | cctgggtaccacctt[C/T]tgagcctcagtttcc | 79446 |
rs1190924 | snp | A/G | 0.296619 | 0.245615 | intron-variant | WDR25 | GRCh38.p7 | 14:100445069 | TGACAGCAAGAACAC[A/G]GAGGCCCAGTTCCAT | 79446 |
rs1190925 | snp | A/G | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100432655 | tgggagtaaaggact[A/G]tcagtcttactctta | 79446 |
rs1190926 | snp | A/C | 0.425586 | 0.17796 | intron-variant | WDR25 | GRCh38.p7 | 14:100432411 | AGTTATTTGCAAGGT[A/C]TCTTTCAGCATGCTA | 79446 |
rs1201468 | snp | C/T | 0.312104 | 0.242163 | intron-variant | WDR25 | GRCh38.p7 | 14:100432639 | tcagtcttactctta[C/T]atggtaccaaaaaat | 79446 |
rs1203548 | snp | A/T | 0.296619 | 0.245615 | intron-variant, upstream-variant-2KB | WDR25 | GRCh38.p7 | 14:100447329 | GGTTGGTGTCCAAAA[A/T]TAAAATCGTTGTAGA | 79446 |
rs1212911 | snp | A/G | 0.438246 | 0.16451 | intron-variant | WDR25 | GRCh38.p7 | 14:100451035 | ACTTGGGCACCTCTA[A/G]TCTCCCAGCTCCCTC | 79446 |
rs1535463 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | WDR25 | GRCh38.p7 | 14:100444284 | CAAACTGCTACCTTC[A/G]AAGTAGCAAAATTTC | 79446 |
rs1535465 | snp | C/T | 0.4628 | 0.13121 | intron-variant | WDR25 | GRCh38.p7 | 14:100426616 | GGCTCAGGGAAGGGG[C/T]AGAGTGAAGAGCTCT | 79446 |
rs1743924 | snp | A/G | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100433849 | aggaaaagaataagt[A/G]agcccagaatatctt | 79446 |
rs1743927 | snp | C/T | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100432276 | TTTTCATAGTGAGTG[C/T]TTCTGCAACATATCT | 79446 |
rs1743928 | snp | A/G | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100449182 | CAAAAATTCCATCCA[A/G]AAGCCCAGTAAAGGA | 79446 |
rs1951522 | snp | A/G | 0.419936 | 0.183362 | intron-variant | WDR25 | GRCh38.p7 | 14:100422216 | ccagaatcactcatc[A/G]gatgctgagcgaaca | 79446 |
rs1957453 | snp | C/G | 0.422 | 0.181428 | upstream-variant-2KB, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100374671 | CACATTCTCTTCTCA[C/G]CTGCTCCAGAATTGG | 79446 |
rs2146104 | snp | C/T | | | intron-variant | WDR25 | GRCh38.p7 | 14:100382016 | TTCTCCCACTAATCA[C/T]TCTCACCTCCTCCCT | 79446 |
rs2181170 | snp | A/G | 0.00077423 | 0.01966 | missense, intron-variant | WDR25 | GRCh38.p7 | 14:100381186 | TGGGGCAAGATCCCC[A/G]ATCGCTTCTCCCAAG | 79446 |
rs2224585 | snp | C/T | 0.284471 | 0.247612 | intron-variant | WDR25 | GRCh38.p7 | 14:100402622 | AGAACACAGTTGAGC[C/T]TCTATGTTTGCCAAG | 79446 |
rs2234517 | snp | G/T | 0.000798403 | 0.0199641 | upstream-variant-2KB, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100375844 | agtaatgcgaccctt[G/T]cccaaggtttcgaat | 79446 |
rs2234518 | snp | C/T | 0.42263 | 0.180829 | upstream-variant-2KB, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100375722 | GGAATTTACAGTTTC[C/T]CTTTCCACCGCCCAC | 79446 |
rs2234519 | snp | A/C | 0.078151 | 0.181571 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100375558 | TTCATTGGTCTCAAC[A/C]TGGCCCCCCAGGCAA | 79446 |
rs2273800 | snp | C/T | 0.422527 | 0.180926 | missense, intron-variant | WDR25 | GRCh38.p7 | 14:100381370 | GACTCACTTTGAGCA[C/T]GGAAAGATGACTTGG | 79446 |
rs2273801 | snp | C/T | 0.0646854 | 0.167805 | missense, intron-variant | WDR25 | GRCh38.p7 | 14:100381100 | GGCTGTGCCCCTGCT[C/T]TGGGCACATCCAGTG | 79446 |
rs2273802 | snp | C/T | 0.464841 | 0.127841 | intron-variant, upstream-variant-2KB, utr-variant-5-prime | WDR25, WARS | GRCh38.p7 | 14:100376562 | CCGCGTTAAGCGGCA[C/T]GGGGCGCTTTAGGCG | 79446 |
rs2273803 | snp | A/G | 0.438386 | 0.164349 | utr-variant-5-prime, upstream-variant-2KB | WDR25, WARS | GRCh38.p7 | 14:100376441 | CACTACCATCCAGTC[A/G]CGTTCCGACGCGACG | 79446 |
rs2273804 | snp | C/G | 0.278399 | 0.248382 | upstream-variant-2KB, utr-variant-5-prime | WDR25, WARS | GRCh38.p7 | 14:100376300 | GCCCAGGAGACAGCC[C/G]GTTGCTGAGCCGGGA | 79446 |
rs2295883 | snp | C/G | 0.448066 | 0.152544 | intron-variant | WDR25, LOC105370664 | GRCh38.p7 | 14:100407706 | GAAACTATGGTCCCT[C/G]TTCTTAGTAATTGTA | 79446 |
rs2400919 | snp | C/T | 0.245265 | 0.249955 | intron-variant | WDR25 | GRCh38.p7 | 14:100415959 | TCCTCCCTGCTCTGC[C/T]GCTGTCCTTCTTTTC | 79446 |
rs2481901 | snp | C/G | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100446061 | CAGGGGGTATAATAT[C/G]TGGGGCAAACACCAA | 79446 |
rs2895869 | snp | A/G | 0.412416 | 0.190055 | intron-variant | WDR25 | GRCh38.p7 | 14:100427519 | CATCTCTGTGAGGCA[A/G]GAGTCCTGGTGCCGA | 79446 |
rs3736825 | snp | C/T | 0.25045 | 0.25 | intron-variant | WDR25 | GRCh38.p7 | 14:100408929 | CTAATAACACTGTAA[C/T]GGAAAAATAATTCAT | 79446 |
rs3742387 | snp | A/G | 0.422181 | 0.181256 | synonymous-codon, intron-variant | WDR25 | GRCh38.p7 | 14:100381593 | TGAGTTTATTCAGCC[A/G]TATTTGAATAGCCAT | 79446 |
rs3742388 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | WDR25 | GRCh38.p7 | 14:100441475 | TCTGGAGCTCTCCAG[A/G]CAGATGCTGGAAGTG | 79446 |
rs3764786 | snp | G/T | 0.078151 | 0.181571 | upstream-variant-2KB, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100374757 | TTGTCACCTACACTC[G/T]GGGGCCAAGATAGAA | 79446 |
rs3835003 | in-del | -/A | 0.422315 | 0.181128 | upstream-variant-2KB, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100374830 | AAAAGGTGTCAAGAA[-/A]TCCTTGCTCTAAAGA | 79446 |
rs3842316 | in-del | -/GGCCCCA | 0.314787 | 0.241459 | intron-variant | WDR25 | GRCh38.p7 | 14:100444571 | AGGCCCCAGGCCCCA[-/GGCCCCA]CCGTACCTGGCAGAT | 79446 |
rs3923757 | snp | C/T | 0.2768 | 0.248559 | intron-variant | WDR25 | GRCh38.p7 | 14:100492243 | GGAGTCCCTGTGTGT[C/T]CCCTGGGTTGTCTAA | 79446 |
rs3934823 | snp | G/T | | | intron-variant | WDR25 | GRCh38.p7 | 14:100482124 | CTCCCATGTGgccag[G/T]ggtgaatatcttcca | 79446 |
rs4072642 | snp | C/T | 0.446641 | 0.154377 | intron-variant | WDR25 | GRCh38.p7 | 14:100482491 | CCAATATATAGATAT[C/T]TGTGTTAAGTTGAAT | 79446 |
rs4379994 | snp | A/G | 0.239902 | 0.249796 | intron-variant | WDR25 | GRCh38.p7 | 14:100385023 | GAATCACCAAGTGCA[A/G]TGCCTGGCACATAGC | 79446 |
rs4900464 | snp | C/T | 0.440471 | 0.161928 | intron-variant | WDR25 | GRCh38.p7 | 14:100399524 | GCATTTCCTCCTTTC[C/T]GTCCCCCTGTGCCCC | 79446 |
rs4905958 | snp | A/G | 0.438386 | 0.164349 | intron-variant | WDR25 | GRCh38.p7 | 14:100457951 | gtctaacaatgggag[A/G]taaaataacaaaaga | 79446 |
rs4905959 | snp | A/C | 0.439085 | 0.163545 | intron-variant | WDR25 | GRCh38.p7 | 14:100464637 | CACCCCATCGCATCA[A/C]CCCAGTGCATTTCAT | 79446 |
rs4905960 | snp | C/T | 0.434543 | 0.168653 | intron-variant | WDR25 | GRCh38.p7 | 14:100465006 | actctcccctacATG[C/T]TCCACCCTCTCTTTG | 79446 |
rs4905961 | snp | A/G | 0.460702 | 0.134554 | intron-variant | WDR25 | GRCh38.p7 | 14:100465298 | TGCAGTCTGCACCCC[A/G]TCTGTCTGCAGAACT | 79446 |
rs4905962 | snp | C/T | 0.472052 | 0.11486 | intron-variant | WDR25 | GRCh38.p7 | 14:100466692 | CTGCCAGCAGCCGTA[C/T]CAGGTGGGAGGCACT | 79446 |
rs4905963 | snp | A/G | 0.4983 | 0.0291038 | intron-variant | WDR25 | GRCh38.p7 | 14:100467134 | TTCTCTCCTCCAACA[A/G]AAGGACAGCTGCCCC | 79446 |
rs4905964 | snp | C/T | 0.442791 | 0.15916 | intron-variant | WDR25 | GRCh38.p7 | 14:100467291 | TGCCAGGGATGCAGG[C/T]GAGCCTGGGATAAGA | 79446 |
rs4905965 | snp | A/G | 0.459233 | 0.136827 | intron-variant | WDR25 | GRCh38.p7 | 14:100467447 | GGCTGCAGGGATGAA[A/G]CAGGTGTGAAGGGCT | 79446 |
rs4905966 | snp | C/T | 0.499563 | 0.0147699 | intron-variant | WDR25 | GRCh38.p7 | 14:100468265 | AGCTGTATACGCTTG[C/T]GTGGCAGAGGGAGAG | 79446 |
rs4905967 | snp | G/T | 0.420415 | 0.182917 | intron-variant | WDR25 | GRCh38.p7 | 14:100468552 | CATTATCGTTGAAAG[G/T]CTGTGAGAAATGATT | 79446 |
rs4905968 | snp | C/G | 0.474363 | 0.110278 | intron-variant | WDR25 | GRCh38.p7 | 14:100472052 | TCCCCCGGAGAGCTC[C/G]CTCAGTTCTAAGCGG | 79446 |
rs4905969 | snp | A/G | 0.293294 | 0.246223 | intron-variant | WDR25 | GRCh38.p7 | 14:100527625 | GAGCTGGAGGGGCAC[A/G]TCTGGCCTCTGAGGG | 79446 |
rs5810995 | in-del | -/C | | | intron-variant | WDR25 | GRCh38.p7 | 14:100389546 | GCCGGGGGACAGAAG[-/C]CCTGAGGGGCAGTCA | 79446 |
rs5810996 | in-del | -/C | 0.44768 | 0.153045 | intron-variant | WDR25 | GRCh38.p7 | 14:100403041 | CTGTATTAGCAGTGT[-/C]CCAACAAATGGTTGT | 79446 |
rs5810997 | in-del | -/T | 0.0887219 | 0.191022 | intron-variant | WDR25 | GRCh38.p7 | 14:100461905 | CGTTGTATTTTTCTG[-/T]TTTTTTTTGTTTGTT | 79446 |
rs5810998 | in-del | -/TG | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100484483 | GTGTGTGTGTGTGTG[-/TG]CGTGTGTGTGTGTGC | 79446 |
rs6420937 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | WDR25 | GRCh38.p7 | 14:100488555 | GGCAGGCCAAGCCAC[A/G]CCTCCAAAGTAGCGT | 79446 |
rs6575776 | snp | A/G | 0.029116 | 0.117091 | intron-variant | WDR25 | GRCh38.p7 | 14:100389673 | TGAACTTGGCAGAGG[A/G]CAGCGTACCTTGATC | 79446 |
rs6575777 | snp | C/T | 0.166506 | 0.235645 | intron-variant, nc-transcript-variant | WDR25, LOC105370664 | GRCh38.p7 | 14:100406179 | AAGCCTTCCTTCTGA[C/T]GTTGATATGTGTGTC | 79446 |
rs6575778 | snp | C/T | 0.115788 | 0.21092 | intron-variant | WDR25 | GRCh38.p7 | 14:100428921 | AGAGGCGTCATCCCC[C/T]GAGCCACTCTGAGTC | 79446 |
rs6575779 | snp | A/G | 0.0988009 | 0.199095 | intron-variant | WDR25 | GRCh38.p7 | 14:100439812 | CATTCAATATAATAA[A/G]TGTTATCTTGAATGT | 79446 |
rs6575780 | snp | C/T | 0.0988009 | 0.199095 | intron-variant | WDR25 | GRCh38.p7 | 14:100439945 | GGGAGTTGCCCAAAC[C/T]CCACTTCCAGTTGGA | 79446 |
rs6575782 | snp | A/T | 0.472052 | 0.11486 | intron-variant | WDR25 | GRCh38.p7 | 14:100467765 | TGCTGGGACTACAGA[A/T]GTGAGCTGCCATACC | 79446 |
rs6575783 | snp | A/T | 0.0484264 | 0.147879 | intron-variant | WDR25 | GRCh38.p7 | 14:100467989 | ATCAGGCCCTTGTTG[A/T]GACACCTGGTGCTGT | 79446 |
rs6575784 | snp | C/T | 0.460589 | 0.13473 | intron-variant | WDR25 | GRCh38.p7 | 14:100495681 | gggcagtggtttgcc[C/T]tacgatctcacttct | 79446 |
rs6575785 | snp | C/T | 0.276534 | 0.248588 | intron-variant | WDR25 | GRCh38.p7 | 14:100500826 | AGCCTAGTTTTAATT[C/T]GTGCCTCCGCTATAA | 79446 |
rs6575786 | snp | A/G | 0.460925 | 0.134204 | intron-variant | WDR25 | GRCh38.p7 | 14:100520460 | TTCTCTTTGTTCACA[A/G]TGTATATCTAATTAG | 79446 |
rs7141055 | snp | A/G | 0.116138 | 0.211142 | intron-variant | WDR25 | GRCh38.p7 | 14:100452253 | actcaagagacattg[A/G]gcttctagtatatgc | 79446 |
rs7141382 | snp | A/C/G | 0.0138799 | 0.0821421 | intron-variant | WDR25 | GRCh38.p7 | 14:100430807 | CCCCAGCCTGGCAAC[A/C/G]TGGACATTTCTGGCT | 79446 |
rs7141858 | snp | C/T | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100452173 | TTCTGTTCCATTCCA[C/T]TCCTTCATGTatcca | 79446 |
rs7142064 | snp | C/T | 0.498982 | 0.0225409 | intron-variant | WDR25 | GRCh38.p7 | 14:100469842 | CAGCAAGTGACAGAG[C/T]CAGGATGCACGCAGG | 79446 |
rs7142209 | snp | C/T | 0.499663 | 0.0129749 | intron-variant | WDR25 | GRCh38.p7 | 14:100527708 | CCTGAACTATAGTTA[C/T]ACTCCACACTGTCTG | 79446 |
rs7142684 | snp | C/T | 0.121369 | 0.214369 | intron-variant, upstream-variant-2KB | WDR25 | GRCh38.p7 | 14:100396077 | cgccttccgggttca[C/T]gacattctcctgcct | 79446 |
rs7143006 | snp | A/T | 0.281841 | 0.247964 | upstream-variant-2KB, utr-variant-5-prime, intron-variant | WDR25, WARS | GRCh38.p7 | 14:100375363 | GCCCTGCCCAGCCAG[A/T]AATGGTCTTTAATAC | 79446 |
rs7144016 | snp | C/T | 0.0573587 | 0.15934 | intron-variant | WDR25 | GRCh38.p7 | 14:100399929 | CAGATGAGGAGGGTA[C/T]GGGTGCTGCAGGTTC | 79446 |
rs7144681 | snp | G/T | 0.460477 | 0.134905 | intron-variant | WDR25 | GRCh38.p7 | 14:100515636 | TTCTATTTATTATTA[G/T]TATTATTTTTGAGAC | 79446 |
rs7144855 | snp | C/G | 0.0980852 | 0.198549 | intron-variant | WDR25 | GRCh38.p7 | 14:100400292 | CGTACAACCCACATG[C/G]CTGCACATTAACTGG | 79446 |
rs7144995 | snp | C/T | 0.153332 | 0.230554 | intron-variant | WDR25 | GRCh38.p7 | 14:100488345 | TGGAACCCAGGATGC[C/T]TGTGGTCTGACCTTT | 79446 |
rs7146840 | snp | A/G | 0.467946 | 0.122472 | intron-variant | WDR25 | GRCh38.p7 | 14:100483465 | CATTTATCGCCCAGC[A/G]TCTCAGGCCACCCCA | 79446 |
rs7147860 | snp | C/G | 0.0726307 | 0.176182 | intron-variant | WDR25 | GRCh38.p7 | 14:100500637 | CGCTGGCTCAGCCAA[C/G]CGAGCCTCACCATCT | 79446 |
rs7148488 | snp | A/G | 0.454904 | 0.143228 | intron-variant | WDR25 | GRCh38.p7 | 14:100455451 | taattgagctccaga[A/G]gagaggagggagaga | 79446 |
rs7148571 | snp | C/G | 0.0283406 | 0.115616 | intron-variant | WDR25 | GRCh38.p7 | 14:100463848 | gccctcatatcctac[C/G]tccagtccagggaag | 79446 |
rs7148655 | snp | A/G | 0.475613 | 0.107697 | intron-variant | WDR25 | GRCh38.p7 | 14:100479705 | TCTTTGTCCATATCA[A/G]CAGGGATCCCCAACC | 79446 |
rs7149402 | snp | A/G | 0.0418186 | 0.138422 | intron-variant | WDR25 | GRCh38.p7 | 14:100494253 | tatttttgttacagt[A/G]cttttgatctcaagc | 79446 |
rs7150047 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | WDR25 | GRCh38.p7 | 14:100494062 | gcattcttcaAtttt[C/T]atttcttgtttttgg | 79446 |
rs7150124 | snp | C/G | 0.444931 | 0.15653 | intron-variant | WDR25 | GRCh38.p7 | 14:100393723 | TGGAGGGGTGTAGTG[C/G]AGGTTGGAGCCCATG | 79446 |
rs7150207 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | WDR25 | GRCh38.p7 | 14:100464027 | ctggagtggtcctAC[C/T]GCAGTGGAACCAGCC | 79446 |
rs7151597 | snp | A/C | 0 | 0 | intron-variant | WDR25 | GRCh38.p7 | 14:100467945 | GAGACCTTTTTCTTT[A/C]TACAGTGGGGTCGAG | 79446 |
rs7153197 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | WDR25 | GRCh38.p7 | 14:100410387 | TGTGGGCTCAGGGGG[C/T]GGAGAGAACATCGAG | 79446 |
rs7153733 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | WDR25 | GRCh38.p7 | 14:100432862 | acatgaacctagatg[A/G]tacagcctactacac | 79446 |
rs7154022 | snp | A/G | 0.140581 | 0.224783 | intron-variant | WDR25 | GRCh38.p7 | 14:100433280 | caagccagttatttt[A/G]tagaccttcaatgta | 79446 |
rs7154961 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | WDR25 | GRCh38.p7 | 14:100495094 | gggcgtggtggctca[C/T]gcctgtaatcccagc | 79446 |