SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6160864 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Wdr25 | GRCm38.p3 | 12:108943702 | AGCCCTTGGGGCAGA[C/T]GACCTCCTATCCTGA | 212198 |
rs6161324 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Wdr25 | Mm_Celera | 12:108943724 | CTATCCTGAGCCTGC[A/C]TGAGCTCTGACTGCT | 212198 |
rs6162494 | snp | A/C | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108943949 | ttacaagtttgagca[A/C]agccttggctacgta | 212198 |
rs13481642 | snp | A/G | 0.295619 | 0.245802 | missense | Wdr25 | Mm_Celera | 12:108898351 | CTCAAACCTTCTCAT[A/G]ATCAAAGCACATTTG | 212198 |
rs29122887 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdr25 | Mm_Celera | 12:108910265 | GACCAAAAGGCTTAA[C/T]GAATGTGGTCTTAAG | 212198 |
rs29122958 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109018273 | GTCCTTCCAGGACCC[A/C]CATCACCCCATCACT | 212198 |
rs29123552 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Wdr25 | Mm_Celera | 12:108911392 | TCCTCACCTTTCTGG[G/T]CCATGACATCTGTCA | 212198 |
rs29124098 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Wdr25 | GRCm38.p3 | 12:109018696 | TTTATGTCACAGGCC[C/T]GTGTAGTGTCCTAAC | 212198 |
rs29127316 | snp | A/G/T | 0.231111 | 0.249285 | intron-variant | Wdr25 | GRCm38.p3 | 12:108896175 | CATAAAAAAAGAAGC[A/G/T]GGCTAGCTGGTCCAT | 212198 |
rs29129458 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:108973402 | GACCCACGTGGGAGC[A/G]TATGTGTCATGGTGC | 212198 |
rs29130411 | snp | G/T | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108905146 | CCTTTCCTCACACTT[G/T]CCCTCGTCTCTCCTG | 212198 |
rs29132622 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Wdr25 | Mm_Celera | 12:108986019 | CTTCTCCTTGCTGAC[C/T]TATCTCCCGCCTTTC | 212198 |
rs29132775 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr25 | Mm_Celera | 12:108916805 | GCACTTGGCTTCTGG[A/G]CCGCCATGGAGCTGG | 212198 |
rs29134816 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdr25 | Mm_Celera | 12:109021525 | CTCTCCGTGCTCTCC[A/G]TGGCGTACGCTGGGC | 212198 |
rs29135364 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Wdr25 | Mm_Celera | 12:108902118 | CACTGATGGGAAGAG[C/T]TAGACCTGAGCCCAG | 212198 |
rs29135732 | snp | G/T | 0.492188 | 0.0620098 | intron-variant, upstream-variant-2KB | Wars, Wdr25 | GRCm38.p3 | 12:108893396 | TTCCCAAAAGCATTT[G/T]AGCCATTTGCCCAGC | 212198 |
rs29137488 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr25 | Mm_Celera | 12:109023308 | GAGGGGAAGGGTGAG[C/T]GGAGGTATCTTAACA | 212198 |
rs29137556 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:108930005 | AAACCCATGAGCCAC[A/C/T]GTGCCCATGCATGAG | 212198 |
rs29140535 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr25 | Mm_Celera | 12:108972006 | GCATTTTACCATAAC[A/G]CAGCGGACACACGAG | 212198 |
rs29140929 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Wdr25 | Mm_Celera | 12:108984471 | GGTCCAGGGCTTGCT[C/T]CTGCTCTTCTGTGTC | 212198 |
rs29141826 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr25 | GRCm38.p3 | 12:108897607 | AGCTTGTACATGCGA[A/G]TGCAGGTAGTCATGG | 212198 |
rs29144118 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Wdr25 | GRCm38.p3 | 12:109019270 | GGTTTAAATAATTTA[C/T]ATACAAAGTGATTAT | 212198 |
rs29145280 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Wdr25 | Mm_Celera | 12:109024442 | ACCAATGTAAGCTGT[G/T]TTCTGAGACTTGAGT | 212198 |
rs29145408 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdr25 | Mm_Celera | 12:109006838 | TGGGCTGGCAGTAGC[C/T]GAGTCTCTTTCCCTG | 212198 |
rs29147294 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109003119 | GGTGTGACTGCTCCA[G/T]CTGGCCGGCCTGCCC | 212198 |
rs29147828 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Wdr25 | Mm_Celera | 12:109028654 | GGGAGGGGAGGGGGG[A/G]GGAGGAGGAAGGAGG | 212198 |
rs29148049 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:109018397 | GTGGCAGGGCCTCAG[C/T]AATACTGGGAGTGGG | 212198 |
rs29150845 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr25 | GRCm38.p3 | 12:109008328 | AGGGCCAGGAACACC[C/T]GAGGGGCTGGCACAT | 212198 |
rs29151201 | snp | A/G | 0.5 | 0 | intron-variant | Wdr25 | Mm_Celera | 12:108905866 | AGCAACCTCTTAGGG[A/G]ACCCAGGAGGGAGCT | 212198 |
rs29153458 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Wdr25 | Mm_Celera | 12:108918485 | ACCTCTCTTTATTGC[A/G]CAAATGCTGCCTGGA | 212198 |
rs29155421 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:109024584 | TCGTTGCTGGATGGC[A/G]CTATTTATTAGGTAC | 212198 |
rs29157522 | snp | C/T | 0.5 | 0 | intron-variant | Wdr25 | Mm_Celera | 12:108925668 | GGACCATAAATACCC[C/T]GAGAACTGTGGTGCA | 212198 |
rs29158485 | snp | C/T | 0.415225 | 0.187619 | upstream-variant-2KB, intron-variant, utr-variant-5-prime | Wars, Wdr25 | Mm_Celera | 12:108895390 | GCCTCTTTTGTGAGT[C/T]TACCCTGCAGATAAC | 212198 |
rs29158529 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109006402 | TACCAGACTCAAAGA[C/T]GCTGCAGGAAATGCC | 212198 |
rs29158925 | snp | C/G/T | 0.492188 | 0.0620098 | intron-variant | Wdr25 | GRCm38.p3 | 12:108972005 | TGCATTTTACCATAA[C/G/T]GCAGCGGACACACGA | 212198 |
rs29159613 | snp | C/G | 0.484429 | 0.0868505 | intron-variant | Wdr25 | GRCm38.p3 | 12:108901986 | CTGGCAGATGTGGGG[C/G]ACTATTGAGCAAGAA | 212198 |
rs29163225 | snp | A/G | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108928744 | AGGGGACTCCTCTAG[A/G]AGGAACAGCACAACT | 212198 |
rs29164241 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Wdr25 | GRCm38.p3 | 12:108930373 | TTTTGTTGATGGGCA[G/T]CTTCTTTGTTTCCAA | 212198 |
rs29165485 | snp | A/C/G | 0.465374 | 0.126941 | intron-variant | Wdr25 | GRCm38.p3 | 12:108936146 | TGTCTTGCCAGTAAA[A/C/G]TTGTGGCACTCGTGT | 212198 |
rs29166918 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Wdr25 | GRCm38.p3 | 12:108917956 | TGGGTAGTTTCCTGC[C/T]CTTTATGGCTGCCTC | 212198 |
rs29167534 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdr25 | Mm_Celera | 12:108904495 | GACACCTTTATGCTC[A/T]CTTTTCATTTCTCCG | 212198 |
rs29169472 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109008437 | TGGGACTAGGGAGTG[C/T]CACTGGCCCTTCTGC | 212198 |
rs29175618 | snp | C/G | 0.207612 | 0.24638 | intron-variant | Wdr25 | Mm_Celera | 12:109008449 | GTGCCACTGGCCCTT[C/G]TGCTTCGTCCCTTTC | 212198 |
rs29176084 | snp | C/T | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108918118 | CTTACTTTGCTTCTG[C/T]TACTGGGGGAAACAT | 212198 |
rs29177986 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:109018270 | ACGGTCCTTCCAGGA[C/G]CCCCATCACCCCATC | 212198 |
rs29178267 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Wdr25 | Mm_Celera | 12:108919333 | ACCCATCTGTACCTC[A/G]GCTCCCTTAAATGCC | 212198 |
rs29179400 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr25 | GRCm38.p3 | 12:109006824 | GCAGAAATGCCGCCT[A/G]GGCTGGCAGTAGCTG | 212198 |
rs29181258 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Wdr25 | Mm_Celera | 12:109016856 | GGGTAACGTCAGTGG[A/G]TAAAGATGCCTGCCA | 212198 |
rs29181460 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Wdr25 | GRCm38.p3 | 12:108903296 | CATCCAAAGGATGGC[C/T]TCGGGCAAAGACACT | 212198 |
rs29182415 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Wdr25 | GRCm38.p3 | 12:109018509 | TGCTCTCCCTAAATG[A/G]CACAACTGGCAGGGG | 212198 |
rs29182416 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Wdr25 | Mm_Celera | 12:108907113 | TGAAAGCAGTGCAGT[A/G]GCTAGCCCTGTGTGC | 212198 |
rs29189457 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:108933156 | GGTGTCAGTCTATAG[C/T]TGTACCTGTAGTGCT | 212198 |
rs29189889 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Wdr25 | GRCm38.p3 | 12:109007994 | TCTGTCCCTTTGCAG[C/T]TTGTGTAGTTCAGGG | 212198 |
rs29191186 | snp | A/G | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108997126 | GACACAGACCCAGCT[A/G]TCTGGGCCCACCACA | 212198 |
rs29191281 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdr25 | Mm_Celera | 12:109018998 | GATTAGCTTTAATAC[A/G]GTGCGCCTTTCAACC | 212198 |
rs29192839 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:109018399 | GGCAGGGCCTCAGCA[A/G]TACTGGGAGTGGGAG | 212198 |
rs29192910 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:108928409 | GCAGCACCTGGCTCT[C/T]GGGCCTCTCTGAACA | 212198 |
rs29193305 | snp | A/G | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108919798 | ACCTGTGCAGCTCTC[A/G]CGATGGTCGTGGCTT | 212198 |
rs29193651 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Wdr25 | GRCm38.p3 | 12:108896528 | TCTGCAGTTGCTCTG[C/T]TTCTCTGGACACGGA | 212198 |
rs29193899 | snp | A/C | 0.188366 | 0.242283 | intron-variant | Wdr25 | Mm_Celera | 12:109017350 | GATCTGATTCCTTCG[A/C]AGTTCTCTTGGTTTG | 212198 |
rs29195579 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:108900884 | TAGTGGATCTGATAC[C/T]TCCAGACAGACAGAC | 212198 |
rs29196799 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr25 | GRCm38.p3 | 12:109019440 | GGCTCACATCTACTG[A/C]CCTCCTCCTTTCTCC | 212198 |
rs29197032 | snp | C/G | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108918244 | TTGGGGGTGCTCTCT[C/G]TAGTTCAGCTTTTCT | 212198 |
rs29197704 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109024621 | CGAGGTGGGAGCCCC[C/T]GTCCCTAATGTGAGT | 212198 |
rs29197877 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Wdr25 | GRCm38.p3 | 12:109016833 | CAGGGTTAGTGGGCC[A/G]GCTCAGTGGGTAACG | 212198 |
rs29197927 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr25 | GRCm38.p3 | 12:108908478 | AAGGATCTTGGGTTG[C/T]TGTGCCTGCTCCTGA | 212198 |
rs29199274 | snp | C/G | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:109023927 | GCCTCACCTCATTTG[C/G]TAGCCAGCGGAACGG | 212198 |
rs29199750 | snp | A/C | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:109009058 | CATGGAGAGAGGCTG[A/C]GGTGGAATCTTCAGT | 212198 |
rs29200612 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wdr25 | GRCm38.p3 | 12:108925059 | AGCCTTGGCCAGCTC[A/G]AGGTAATGGTGGAGA | 212198 |
rs29201074 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Wars, Wdr25 | Mm_Celera | 12:108892459 | CATTATCTGTGAGCA[G/T]ATAGGAAAGAGAAGG | 212198 |
rs29203968 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109006240 | CTGCACATGAGAAAC[C/T]GTGAGCGCTGGCCTA | 212198 |
rs29204388 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:109024485 | TGTTCCCTGTGTCAC[A/T]GCTACTCGTCCAGGG | 212198 |
rs29204713 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Wdr25 | Mm_Celera | 12:109013987 | CCTCTGTTCACTTTG[A/G]TGAGTTCTATAGTTC | 212198 |
rs29205022 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr25 | GRCm38.p3 | 12:109018275 | CCTTCCAGGACCCCC[A/G]TCACCCCATCACTTG | 212198 |
rs29205102 | snp | A/T | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:109023954 | ACGGATGACCCCAGA[A/T]CTGTGTGTCTGCTGT | 212198 |
rs29205573 | snp | C/T | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108933093 | CTATAGCTGTACCTG[C/T]AGTGCTTGCCTGGTG | 212198 |
rs29205960 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Wdr25 | Mm_Celera | 12:108984022 | TCCCATCTAGGGAGG[A/G]CTTCTTCATCTTCAT | 212198 |
rs29206007 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:108971387 | TCATTGAGCTAAGAA[C/T]AAGCATGCCTATGGC | 212198 |
rs29206267 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Wdr25 | Mm_Celera | 12:109028952 | AGGGCCTTGGGTTGG[A/G]CCTTGCCCCAAGGCT | 212198 |
rs29206314 | snp | C/T | 0.492188 | 0.0620098 | intron-variant, upstream-variant-2KB | Wars, Wdr25 | GRCm38.p3 | 12:108893479 | GGCGGCTGAGGCCAA[C/T]CAAACTCTCAAGAGC | 212198 |
rs29211615 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr25 | GRCm38.p3 | 12:108934107 | CAAGCTCCCACCTGC[C/T]GTTCAAACATCTCTC | 212198 |
rs29213321 | snp | A/C | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:108918002 | TTGGAAGCATCTGCT[A/C]ATCCTCCATGGGAGT | 212198 |
rs29218011 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Wdr25 | GRCm38.p3 | 12:108912256 | TTTCCTTTCCTCTTT[C/T]ATGTGGCCATCTCTT | 212198 |
rs29219737 | snp | A/C | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:109009472 | TCAGCGGAGACCTTC[A/C]CAATGTCAGCAGCCA | 212198 |
rs29219829 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109006330 | GTGCTTCATCTCCAT[C/T]TCCTGCTCACTGGGC | 212198 |
rs29220691 | snp | C/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Wars, Wdr25 | GRCm38.p3 | 12:108893275 | TTTCTTTGTTTGTTT[C/G]TTTCTTTTTTTTTTA | 212198 |
rs29221495 | snp | A/G | 0.493827 | 0.0552116 | intron-variant, downstream-variant-500B | Wdr25 | GRCm38.p3 | 12:109025139 | GATCTTCCATGTGAG[A/G]AACTTTGGATTGAAT | 212198 |
rs29221556 | snp | C/T | 0.5 | 0 | intron-variant | Wdr25 | GRCm38.p3 | 12:109009369 | TGCTGGAGGCTGGTG[C/T]CACTGTGTCAGCTGG | 212198 |
rs29223305 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr25 | GRCm38.p3 | 12:109012858 | TTCTTGTCGACTTTT[C/T]GTGTGAGGTCAATGC | 212198 |
rs29488752 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdr25 | Mm_Celera | 12:109010022 | GGTTGGAACTGGTCA[A/G]GACAGGGCCTCCACC | 212198 |
rs29489681 | snp | C/T | 0.375 | 0.216506 | intron-variant | Wdr25 | Mm_Celera | 12:108933165 | CTATAGCTGTACCTG[C/T]AGTGCTTGCCTGGTG | 212198 |
rs29491478 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdr25 | Mm_Celera | 12:108971096 | TCAGGGTTGCAGCAA[C/G]GGCTCGGTAGTTAAG | 212198 |
rs33845726 | snp | C/T | 0.5 | 0 | intron-variant | Wdr25 | Mm_Celera | 12:108911090 | TCTAATTCTCATACA[C/T]GCTAGTATTAAAAGT | 212198 |
rs36235326 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Wdr25 | Mm_Celera | 12:108933120 | GGTGTCAGTCTATAG[C/T]TGTACCTGCAGTGCT | 212198 |
rs36240691 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Wdr25 | Mm_Celera | 12:108907681 | TACAAAACTGAGATT[A/C]CACAGTCTTCCAGAG | 212198 |
rs36246286 | snp | A/C | 0.486111 | 0.0821678 | intron-variant | Wdr25 | GRCm38.p3 | 12:108973172 | GCAGCAGCTTTGTAG[A/C]ACCGGGTACTTGAGT | 212198 |
rs36246766 | snp | A/G | 0.5 | 0 | intron-variant | Wdr25 | Mm_Celera | 12:108940085 | ACTCACTAACTTGCT[A/G]TTAAAGGCACAAATT | 212198 |
rs36247633 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Wdr25 | GRCm38.p3 | 12:109021516 | ACCCAAGTCCTCTCC[A/G]TGCTCTCCGTGGCGT | 212198 |
rs36248953 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Wdr25 | GRCm38.p3 | 12:108984458 | GTACTGTCTGTCAGG[C/T]CCAGGGCTTGCTTCT | 212198 |
rs36248957 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Wdr25 | GRCm38.p3 | 12:108985230 | CTTCTCTTTCAAAGG[A/G]ATCAGTACTTGGGTT | 212198 |