SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13473834 | snp | A/C | | | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | Mm_Celera | 3:100138368 | TTATTTGTATTAGAG[A/C]TTTTCTGTTTACCGT | 269470 |
rs30067610 | snp | A/C | 0.455 | 0.143091 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100162068 | TTTTCCTTCCTGCGA[A/C]CTGGTCACTCTCAAA | 269470 |
rs30120077 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100162799 | CCAAGCTCTGGGGAC[A/G]CAGGTCCCCGGGATT | 269470 |
rs30152485 | snp | C/T | 0.375 | 0.216506 | intron-variant, missense | Spag17, Wdr3 | GRCm38.p3 | 3:100138730 | CTGTTTTTTCGTTTT[C/T]TCTTCTTCTCTTCCA | 269470 |
rs30153252 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdr3 | Mm_Celera | 3:100158327 | ACAGGACAAGTTTAT[A/G]TGGTACCAGGGACCA | 269470 |
rs30170976 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100161776 | AAGCTCGCAGAGCTT[A/C]TGGGGCTGCTGCAGT | 269470 |
rs30207880 | snp | C/T | 0.495 | 0.0497494 | intron-variant | Wdr3 | Mm_Celera | 3:100148521 | GTAGCCTTTAAATTT[C/T]ACCTATGCTTTACAT | 269470 |
rs30258005 | snp | C/T | 0.456747 | 0.140554 | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | Mm_Celera | 3:100138485 | CTGAAAAATGCAGAT[C/T]TTTAAACTAAATCCG | 269470 |
rs30300646 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100163942 | GTCCTTGAGCTCACA[A/G]AGATCCACCTGCCTC | 269470 |
rs30312689 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142147 | CAAATCATAATGCCT[C/T]CTTACTCCCTCTCAT | 269470 |
rs30467855 | snp | A/C/T | 0.18 | 0.24 | intron-variant, synonymous-codon | Spag17, Wdr3 | Mm_Celera | 3:100141590 | AGTCTCTAACACATA[A/C/T]GCTGAAGGCTACAAA | 269470 |
rs30512224 | snp | C/T | 0.432133 | 0.171253 | missense | Wdr3 | Mm_Celera | 3:100153578 | TGCCTGTCTTGTCCA[C/T]GGCGAGGTTCACAAC | 269470 |
rs30604959 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100160529 | ATAAATCTATATGTA[A/T]CTCATCTCACCTCCT | 269470 |
rs30606460 | snp | C/T | 0.42 | 0.183303 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100139786 | ACTACGTGTGTATTC[C/T]TTAGTTCCCCTCCTT | 269470 |
rs30662376 | snp | A/C | 0.49827 | 0.0293608 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100162747 | GCTGGCGGGTCCTCC[A/C]GGGCTTTGGGCTTCG | 269470 |
rs30674699 | snp | A/G | 0.304688 | 0.243945 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100161694 | AGATATTATCTCTAT[A/G]CAATCACCCTGTCTC | 269470 |
rs30702386 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142150 | ATCATAATGCCTTCT[C/T]ACTCCCTCTCATCTC | 269470 |
rs30752517 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100162227 | GCCGCGGCAAAGGGC[C/T]TCTCCCCGGCCTCCC | 269470 |
rs30757937 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142747 | GATGAAACTATATAG[A/G]GTCACAACAGGGCAG | 269470 |
rs30856978 | snp | A/T | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142749 | TGAAACTATATAGAG[A/T]CACAACAGGGCAGCT | 269470 |
rs30895061 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100139404 | TGCCAGCCATGGGGA[C/T]TGCTGAGAGCTCAGT | 269470 |
rs30944549 | snp | A/G | 0.492188 | 0.0620098 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100162203 | CCTCTGGGTTCTGCG[A/G]TGCAGACGGCCGCGG | 269470 |
rs30996166 | snp | A/T | 0.359862 | 0.224567 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100164165 | TGTTTAATATGTAGG[A/T]GACACTGCTAATTCA | 269470 |
rs31048912 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB, utr-variant-5-prime | Gdap2, Wdr3 | GRCm38.p3 | 3:100162349 | CAACACTCACCTCAC[C/T]CTCCACGAGGCTCCA | 269470 |
rs31091319 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Wdr3 | Mm_Celera | 3:100160415 | GATTTCTGATACAGA[A/G]CTATAAACTCATCCT | 269470 |
rs31139409 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100160580 | GGATAATTTATCTCT[C/T]TGTGCTTAGCAAGAA | 269470 |
rs31175680 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100164211 | TTGTATGTTTTTTTT[A/G]AATGATGATTTACAG | 269470 |
rs31237561 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100163975 | CCTACAGCATGCAGG[A/G]ATTAAAGGCGTGTAC | 269470 |
rs31247217 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdr3 | Mm_Celera | 3:100144268 | CTCTTCACAGGTATA[A/G]GAACCTTAACTAAGG | 269470 |
rs31275649 | snp | C/T | 0.432133 | 0.171253 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100143308 | ACAACTGAATAAAAA[C/T]ACTACATAGAGGCTA | 269470 |
rs31287637 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Wdr3 | Mm_Celera | 3:100157544 | GGTGCTATACTGCCC[A/G]ATACAGCTTGGGGTT | 269470 |
rs31354140 | snp | C/T | 0.473373 | 0.11227 | upstream-variant-2KB, intron-variant | Gdap2, Wdr3 | Mm_Celera | 3:100162307 | CACTGTGCGGGGAAC[C/T]GCGCCCCGCGATCCC | 269470 |
rs31386024 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100162687 | GAAGGGCGAAGCCGG[A/G]AAGGGAGGGCGACAC | 269470 |
rs31387931 | snp | G/T | 0.359862 | 0.224567 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100164294 | TATTTGCTGATATAG[G/T]TGAGCACGGACATGT | 269470 |
rs31431965 | snp | A/G | 0.345679 | 0.230967 | synonymous-codon | Wdr3 | GRCm38.p3 | 3:100151144 | GATTGTTCTGCAGCA[A/G]GAAGACGGCCTTTAA | 269470 |
rs31473177 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdr3 | Mm_Celera | 3:100155709 | TTTGAAGTGGAAAGA[C/T]CAACTTCTACCATGA | 269470 |
rs31473996 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142029 | GGCTGGTCTAGCCCC[A/G]ACGCATCTGGGGAAG | 269470 |
rs31517922 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100141478 | AGAAAGAAAACTATC[A/C]ATTCCAACTTGTATT | 269470 |
rs31544778 | snp | A/C/T | 0.497778 | 0.0332592 | synonymous-codon | Wdr3 | GRCm38.p3 | 3:100150992 | AATGGAATCGGCTGC[A/C/T]GCTGAAAGCACAGCT | 269470 |
rs31545546 | snp | C/T | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100163019 | TGACCCTGGGCTTAC[C/T]GGTCCTTAATTGTAG | 269470 |
rs31576346 | snp | C/T | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | Mm_Celera | 3:100138582 | GTACCCCAAGATCTA[C/T]AACATGATCTTTTTT | 269470 |
rs31693675 | snp | A/G | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Gdap2, Wdr3 | Mm_Celera | 3:100164183 | CACTGCTAATTCACC[A/G]GAAAACATGTGTTTT | 269470 |
rs33317496 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Spag17, Wdr3 | Mm_Celera | 3:100138084 | ATCTGAGTTAATCTA[C/T]TTTTTTCTAGATATC | 269470 |
rs33317499 | snp | A/G | 0.244898 | 0.249948 | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | GRCm38.p3 | 3:100138224 | ATTGTATTTCCAAAA[A/G]TACAAACAGCATTAT | 269470 |
rs33317501 | snp | G/T | 0.142012 | 0.225474 | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | GRCm38.p3 | 3:100138244 | AACAGCATTATGACC[G/T]TACATGCAGACTCAC | 269470 |
rs33317503 | snp | A/G | 0.444444 | 0.157135 | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | GRCm38.p3 | 3:100138258 | CTTACATGCAGACTC[A/G]CCAACCTGCACTGGT | 269470 |
rs33318556 | snp | C/T | 0.336735 | 0.234472 | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | GRCm38.p3 | 3:100138450 | TATTTTGCTTCTTGA[C/T]ACAATTTAAAGGTCC | 269470 |
rs33318561 | snp | A/G | 0.124444 | 0.216185 | intron-variant, utr-variant-3-prime | Spag17, Wdr3 | Mm_Celera | 3:100138645 | TCAGTTTATGTGTAC[A/G]CTCCTTTGAGAAGAA | 269470 |
rs33319294 | snp | C/T | 0.124444 | 0.216185 | intron-variant, synonymous-codon | Spag17, Wdr3 | Mm_Celera | 3:100138708 | CAGTGTTAAAATCAT[C/T]CTTTTCCTGTTTTTT | 269470 |
rs33319297 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100138845 | AGCCAATGGCATCCT[A/G]GAGAAGAATACAAAA | 269470 |
rs33319300 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100138851 | TGGCATCCTGGAGAA[A/G]AATACAAAAAAGTAA | 269470 |
rs33319302 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100138880 | AATCTTTAGTCAGTG[C/T]AGCAGCGTCTGAGTG | 269470 |
rs33319685 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142146 | CCAAATCATAATGCC[G/T]CCTCACTCCCTCTCA | 269470 |
rs33319688 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142281 | AAGACGTTATGAAGG[A/G]AGCCAAGTCATTACA | 269470 |
rs33319691 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142338 | CTTATTCTGACACAC[A/G]GATCATTTACTGCCT | 269470 |
rs33319694 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr3 | Mm_Celera | 3:100146407 | GGTCACACAGAAAGA[A/C]TATTCCCAGACAAAC | 269470 |
rs33319697 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdr3 | Mm_Celera | 3:100146805 | AAAATCAAATGACAC[G/T]TCAGTTAAAAAACAT | 269470 |
rs33319699 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Wdr3 | Mm_Celera | 3:100146957 | TTGAGAATGCCAGCA[C/G]AGACTAACACTGACA | 269470 |
rs33319702 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr3 | Mm_Celera | 3:100147010 | GTCCTTCTTAGCATC[A/G]TGAAGAAAAGCCTTT | 269470 |
rs33319826 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdr3 | Mm_Celera | 3:100150592 | CAAATGCAGCCAAAG[A/C]TACAGATGAAAGAAA | 269470 |
rs33319829 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Wdr3 | Mm_Celera | 3:100150631 | TTATTCTACTCCAAA[A/T]TTTAATTTTTATCTT | 269470 |
rs33319832 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Wdr3 | Mm_Celera | 3:100150735 | CTCCAGGGATCAACT[C/G]AGGTCTTTAGTGGCA | 269470 |
rs33320175 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100138963 | AAAACCCTATCTCTG[C/T]AACAGACAACAGAAA | 269470 |
rs33320177 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100139302 | AAAAATGCAACGTTA[A/T]ATCTGGTAATACAGT | 269470 |
rs33320181 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100139871 | ATTTTTAAAATGTTG[C/G]GAACAAAGCTGACTA | 269470 |
rs33320425 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdr3 | Mm_Celera | 3:100147576 | TTCCCTAGTCATCAC[C/T]GGACTATGGAGGGAA | 269470 |
rs33320428 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr3 | Mm_Celera | 3:100147634 | AGGTGCTAAGAAAAC[A/G]TTCCCCTCTGTAAAG | 269470 |
rs33320431 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr3 | Mm_Celera | 3:100147900 | TGCTGCTGAGGATGA[A/G]CAGTTGAACAACTCA | 269470 |
rs33320484 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142573 | CAAAGGCAGAGATCA[C/T]CCCAGTGCACACCCA | 269470 |
rs33320487 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142594 | TGCACACCCAAGACA[C/T]GGAGATGGGAAGGCC | 269470 |
rs33320489 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142683 | ATTTACAGTTGTCAG[C/T]ATGGTTCTTATTTTT | 269470 |
rs33320491 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142770 | CAGGGCAGCTTCCAG[A/G]AGAACCGACATGAGC | 269470 |
rs33320684 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Wdr3 | Mm_Celera | 3:100150787 | GTCTCACCAGCCCTA[A/C]ACCAAAATTCTAACA | 269470 |
rs33320687 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Wdr3 | Mm_Celera | 3:100150854 | TATCTTCTGACTGAA[C/T]TGTATTTAGATTCTT | 269470 |
rs33320690 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr3 | Mm_Celera | 3:100150894 | AGCCAAAAATGAGAA[A/G]TATCAAAAGTGCTTC | 269470 |
rs33320693 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr3 | Mm_Celera | 3:100150958 | GAAAGCACCAATTCA[C/G]AGACCTGTTCCAGAT | 269470 |
rs33321124 | snp | C/T | 0.32 | 0.24 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100139959 | AATCTACCTAGCCTC[C/T]TTAGACTGCATCCTC | 269470 |
rs33321127 | snp | A/G | 0.32 | 0.24 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100140468 | CACTCAACACCATCC[A/G]TTTAGAGTATGTTAG | 269470 |
rs33321129 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100140526 | ATTGCAGATAAAGTG[C/T]TCACTATGCCTTGCT | 269470 |
rs33321132 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100140813 | ACTTCCAGTTAGAAG[A/T]CGCAAGAGGATTTCA | 269470 |
rs33321264 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdr3 | Mm_Celera | 3:100148051 | CTAAACTTGGCAGAT[C/G]TAAGATGTACTCAGA | 269470 |
rs33321266 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Wdr3 | Mm_Celera | 3:100148094 | ATAGCTTTAAAGCCC[A/G]GTGCAGTTACCTGAT | 269470 |
rs33321269 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Wdr3 | GRCm38.p3 | 3:100148186 | GCCTGAGGCCAGGTC[A/G]TAAAGTTGCAGATTT | 269470 |
rs33321272 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdr3 | Mm_Celera | 3:100148236 | AAAGTTTTAAGGGGC[A/G]CATCCACAGACTTCA | 269470 |
rs33321318 | snp | G/T | 0.32 | 0.24 | synonymous-codon | Wdr3 | GRCm38.p3 | 3:100151069 | CTCCAATGGTGATCC[G/T]GCTTGTCCTCACAGG | 269470 |
rs33321323 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Wdr3 | Mm_Celera | 3:100151257 | CTACTATCTTGGCTC[A/G]TGAAGCCAACATTTT | 269470 |
rs33321354 | snp | A/C | 0.231111 | 0.249285 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100142825 | GGTCAGACGCAAGAC[A/C]ACGGGCATCAGACAA | 269470 |
rs33321357 | snp | C/G | 0.32 | 0.24 | utr-variant-3-prime, intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100143134 | TTTGTATCATCATGA[C/G]CACTATCCTGAAAAT | 269470 |
rs33321362 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B, missense | Spag17, Wdr3 | Mm_Celera | 3:100143405 | AAGATTCACTTACTG[C/T]CGGCTGGTCTTCTTT | 269470 |
rs33321925 | snp | A/C | 0.32 | 0.24 | intron-variant | Spag17, Wdr3 | GRCm38.p3 | 3:100140864 | CTTAGTTTAACAGTT[A/C]TCACCCTTACGAACT | 269470 |
rs33321927 | snp | G/T | 0.32 | 0.24 | intron-variant | Spag17, Wdr3 | GRCm38.p3 | 3:100140900 | CTCCAGTCTTGGCCC[G/T]TGTGTCTGCACCTCT | 269470 |
rs33321929 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spag17, Wdr3 | GRCm38.p3 | 3:100140918 | TGTCTGCACCTCTAT[C/T]CTCCAGGCCCCTTTA | 269470 |
rs33321932 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spag17, Wdr3 | Mm_Celera | 3:100140944 | CTTTACGTTTCTAAC[A/G]AAAGCTCGGCAGTAT | 269470 |
rs33321935 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Wdr3 | Mm_Celera | 3:100148440 | CTTGCAGATCTTGAT[C/T]CTGCCTCTTTTGCTG | 269470 |
rs33321938 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr3 | Mm_Celera | 3:100148478 | ATCACAGCCACAGAC[A/C]AATCTGAACAGTTCA | 269470 |
rs33321943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdr3 | Mm_Celera | 3:100148604 | TTTCTTCTTTTTGCA[A/G]CACACTGACAGTGAG | 269470 |
rs33322052 | snp | A/T | 0.231111 | 0.249285 | intron-variant, downstream-variant-500B | Spag17, Wdr3 | Mm_Celera | 3:100137702 | AGGATACTTTTTACT[A/T]CTGCCCTTGGCTGTG | 269470 |
rs33322195 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdr3 | Mm_Celera | 3:100154599 | GCAATAACCTGAACA[A/G]CACTATTACCAAAAG | 269470 |
rs33322198 | snp | A/C | 0.32 | 0.24 | intron-variant | Wdr3 | Mm_Celera | 3:100154650 | CTTCCAGCTCAAATA[A/C]ACCAGGGCAATGAGT | 269470 |
rs33322201 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Wdr3 | Mm_Celera | 3:100154938 | CTCTTGCAGATAGTC[A/G]ATGTCCCAGGCTCTC | 269470 |