SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6300498 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Herc4 | Mm_Celera | 10:63271623 | AACTCAAATTAGGTG[C/G]TCAGGGNGGTGAGAG | 67345 |
rs6300513 | snp | C/T | 0.5 | 0 | intron-variant | Herc4 | Mm_Celera | 10:63271630 | ATTAGGTGNTCAGGG[C/T]GGTGAGAGCAGCGGG | 67345 |
rs13471355 | snp | A/G | | | intron-variant | Herc4 | GRCm38.p3 | 10:63295721 | acccacatgccttta[A/G]cCTACCCCCAGCTCA | 67345 |
rs29326554 | snp | C/T | 0.5 | 0 | intron-variant | Herc4 | Mm_Celera | 10:63309129 | GAGAAATAGCTCAGC[C/T]TTATTGTTAGGCATC | 67345 |
rs29345704 | snp | A/C | 0.5 | 0 | intron-variant | Herc4 | Mm_Celera | 10:63263383 | CCCTGTCTCAAAAAA[A/C]CCAAAAAAAAAAAAA | 67345 |
rs45697363 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Herc4 | Mm_Celera | 10:63268940 | AGGTCAGGTGGCAGT[A/G]TCAGCTAAAGTCAGA | 67345 |
rs45906281 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Herc4 | Mm_Celera | 10:63274480 | CATTTCATACTTACC[A/G]GTTTTTGAATGCGAA | 67345 |
rs46641605 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Herc4 | Mm_Celera | 10:63313133 | GCACTTAGACTGCCT[A/C]GTAGATGGATTTGTC | 67345 |
rs46647758 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63294222 | TCCTGGATCTGCTTG[C/G]AGCCATGGTCTTTTC | 67345 |
rs46676068 | snp | C/T | | | intron-variant | Herc4 | Mm_Celera | 10:63279749 | AGTTTGAGGCCATCC[C/T]GATCTACAAAGTGAA | 67345 |
rs46722644 | snp | A/C | | | intron-variant | Herc4 | Mm_Celera | 10:63258048 | ATAGCCTGTTATTTT[A/C]TTTCCTTTGCAAATG | 67345 |
rs46771548 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc4 | Mm_Celera | 10:63269498 | GAAGTTTTGATAATT[A/G]GCCGTGACTGAAAGA | 67345 |
rs46796073 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Herc4 | Mm_Celera | 10:63308875 | GGACCCCGTGTTCAG[C/T]TAAGACTAAGATGTT | 67345 |
rs46829084 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63291509 | TCCAGACTGGGGACC[A/G]TTACTTTACCTGCTT | 67345 |
rs46853757 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63308839 | TGACACGTGTGCATG[A/G]GAGACAGCTGATAGT | 67345 |
rs46859672 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Herc4 | Mm_Celera | 10:63309088 | ACTGCACTGGAATTA[C/T]ACTGTCTTGGGTGCT | 67345 |
rs46889856 | snp | C/T | 0.336735 | 0.234472 | upstream-variant-2KB | Herc4 | Mm_Celera | 10:63243633 | CCCTAGCCGGCTGCA[C/T]TAGCGTCTTAGAGCA | 67345 |
rs47093458 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63292485 | CCAGATGCTAGGATT[A/G]GCCTCCTTGTTAGTT | 67345 |
rs47133638 | snp | G/T | 0.152778 | 0.230321 | intron-variant | Herc4 | Mm_Celera | 10:63269760 | TCTGAACAAAAGGCC[G/T]CTGGGTTTTCTTTTA | 67345 |
rs47165704 | snp | C/T | 0.391111 | 0.206368 | intron-variant, utr-variant-3-prime | Herc4 | Mm_Celera | 10:63290306 | ACTTTCGAGAGATTT[C/T]TAAGAACAATATCCT | 67345 |
rs47348955 | snp | C/G | | | intron-variant | Herc4 | Mm_Celera | 10:63268143 | AACTCAGATCCACTC[C/G]CCTTTGCTGAGATTA | 67345 |
rs47464548 | snp | C/G | 0.408163 | 0.193609 | utr-variant-3-prime, nc-transcript-variant | Herc4 | Mm_Celera | 10:63317812 | CTACGATGGCCTGCC[C/G]ACAGTCATTTGATTA | 67345 |
rs47612397 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63311965 | TCTCGTTCCATAGAG[C/T]AAATGCTTTTTGTTG | 67345 |
rs47659326 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63246969 | GAGGAGAAAGCTGCC[C/G]TGCTGTTTGTCACAG | 67345 |
rs47715906 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63311295 | GCCTGGGACTGTGCC[A/G]AATGATGTTCATGCT | 67345 |
rs47792361 | snp | A/G | 0.132653 | 0.220748 | utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant | Herc4 | Mm_Celera | 10:63244108 | GAGAGCCGCCCAGAG[A/G]TCCAGGGAGCGTCCG | 67345 |
rs48001636 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Herc4 | Mm_Celera | 10:63294775 | CTTGGGAAATATTTC[C/T]AATGCTCTAAATGGC | 67345 |
rs48077758 | snp | A/G | 0.42 | 0.183303 | intron-variant | Herc4 | Mm_Celera | 10:63273185 | GAGTAAGAGAGATGA[A/G]GAATGTTAGAGAGTC | 67345 |
rs48183135 | snp | A/C | | | intron-variant | Herc4 | Mm_Celera | 10:63279565 | ACCATCTATATCTCC[A/C]GTTGCAAGGGATCCA | 67345 |
rs48183541 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Herc4 | Mm_Celera | 10:63308829 | ACTACTGCTTTGACA[C/T]GTGTGCATGGGAGAC | 67345 |
rs48198676 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63309073 | TAAGGGCAACAAACT[A/C]CTGCACTGGAATTAT | 67345 |
rs48294508 | snp | G/T | | | intron-variant | Herc4 | Mm_Celera | 10:63246783 | GAGATCTAAGCACAA[G/T]GTAAAATAATTTATC | 67345 |
rs48380713 | snp | C/T | | | intron-variant | Herc4 | Mm_Celera | 10:63312476 | GTCAGAAAGCAGGAG[C/T]TGATGCAGAGGCCAT | 67345 |
rs48439450 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Herc4 | Mm_Celera | 10:63313299 | CCAGACCTCTTAGAT[C/T]GTTGTAAGATTGGAA | 67345 |
rs48579583 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Herc4 | Mm_Celera | 10:63271464 | AGCTATGACCACTGG[A/C]CCTCACAGCATCACA | 67345 |
rs48607866 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63313505 | CACATTCGCATATTC[A/G]GACCTACACACCTCA | 67345 |
rs48901220 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63279537 | CTGTTCCCAGCATGT[A/G]TGTTGTCTCACAACC | 67345 |
rs49046733 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63293144 | CTCACATATCAGGTG[A/G]CTCACAACTTCCTAC | 67345 |
rs49065689 | snp | C/T | | | intron-variant | Herc4 | GRCm38.p3 | 10:63295905 | CCGTCCTTGGCTACA[C/T]GCAGAGACCTTATTA | 67345 |
rs49088256 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Herc4 | Mm_Celera | 10:63262492 | GTTTGACTTGCTTTT[A/G]TCATGAGGCTTCTGG | 67345 |
rs49141503 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Herc4 | Mm_Celera | 10:63274676 | GTTTTGCCACAAAGT[A/G]CAGAAAGTAGATCAG | 67345 |
rs49225327 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Herc4 | Mm_Celera | 10:63295006 | GGCCAGGAACCTTCA[A/G]ACTGAATGGATAGAA | 67345 |
rs49533970 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63269840 | TTCTATGTTTACAAA[A/G]CTGCTGAAATATTTG | 67345 |
rs49661388 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Herc4 | Mm_Celera | 10:63294805 | CGTCATGGAAAATAC[C/T]TTTGATGTCTGCTGT | 67345 |
rs49734769 | snp | A/G | 0.375 | 0.216506 | intron-variant | Herc4 | Mm_Celera | 10:63266538 | TTTTTGTCTGTTGAA[A/G]AACTTTGTACATTTA | 67345 |
rs49781118 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63269838 | GTTTCTATGTTTACA[A/G]AGCTGCTGAAATATT | 67345 |
rs49926980 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant | Herc4 | Mm_Celera | 10:63311592 | GCTGAAAAGGAAGCC[A/G]TCCCTGGATGATCTG | 67345 |
rs49990245 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Herc4 | Mm_Celera | 10:63311577 | TTTATATAAGAAACT[A/G]CTGAAAAGGAAGCCG | 67345 |
rs50071097 | snp | A/G | | | intron-variant | Herc4 | GRCm38.p3 | 10:63296003 | TGTGATTTTGTGTTT[A/G]TGTTTTTAGTAAAGA | 67345 |
rs50216714 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Herc4 | Mm_Celera | 10:63292150 | TATTAAGATTCCATC[A/G]TCACCTTTTTTATAA | 67345 |
rs50251795 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Herc4 | Mm_Celera | 10:63274673 | ATTGTTTTGCCACAA[A/G]GTGCAGAAAGTAGAT | 67345 |
rs50428686 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63294023 | CACTACTTTTATTTA[C/T]TGGGTTAGACAGAAA | 67345 |
rs50435277 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63260018 | TTTGCCACCACTTCA[A/G]CTCTGTTTTTTTTCC | 67345 |
rs50458246 | snp | C/T | | | intron-variant | Herc4 | Mm_Celera | 10:63268167 | GAGATTAAAGGCCTG[C/T]TCCACCATGCCGAGC | 67345 |
rs50522740 | snp | A/G | 0.260355 | 0.249785 | downstream-variant-500B | Herc4 | Mm_Celera | 10:63318120 | GCCACCACGCCCGGC[A/G]GAAATGATCTTTTTG | 67345 |
rs50593249 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Herc4 | Mm_Celera | 10:63295037 | CATAGATTGATTCAT[C/T]ATAATTACCCCATAA | 67345 |
rs50611746 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63288037 | GTGCTTGTATATTTA[C/T]TATTTAGCTGCTGGA | 67345 |
rs50681130 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63293901 | CTGGCTTGATGACAA[A/G]TGCCTTTATGTGCTA | 67345 |
rs50773111 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Herc4 | Mm_Celera | 10:63263026 | GTGCTAAAATAGAAA[C/T]CCATAAACTAAGACC | 67345 |
rs50848777 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc4 | Mm_Celera | 10:63291741 | TGAAGATCTTCTCAC[A/G]TGGTAGCAGGGCTCT | 67345 |
rs50880567 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Herc4 | Mm_Celera | 10:63313320 | AAGATTGGAACGTCC[A/G]GCGTGTTTGCAAGGA | 67345 |
rs50958451 | snp | A/G | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Herc4 | Mm_Celera | 10:63245769 | TTTAGCTTAACACTC[A/G]ATGAGAGAGCAGCTT | 67345 |
rs51086137 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Herc4 | Mm_Celera | 10:63287321 | AGTCACTAAGTCATC[G/T]CTGGCCCCATTAAAA | 67345 |
rs51133770 | snp | A/C/G | 0.408163 | 0.193609 | intron-variant | Herc4 | GRCm38.p3 | 10:63287689 | ACATATGTATAGTGT[A/C/G]CTTTGATGAGACAAC | 67345 |
rs51144202 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Herc4 | Mm_Celera | 10:63257964 | CTCACACCTGAGATT[C/G]ATCTTGGGCTCCTTT | 67345 |
rs51190346 | snp | C/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Herc4 | Mm_Celera | 10:63245684 | AACATTTGTATATGG[C/T]CCTTTAAAACTGAGA | 67345 |
rs51193599 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Herc4 | Mm_Celera | 10:63291551 | CCTGGGTCTTTTTCT[C/T]CACTACTTAACTTCC | 67345 |
rs51317625 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63287628 | AAACTTGAGTGATGT[A/G]TTAAAGAACTAATTA | 67345 |
rs51343686 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB | Herc4 | Mm_Celera | 10:63242702 | CAGTAAAGCCATAAC[A/G]CTGTGTAAAACTAAC | 67345 |
rs51433291 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63291918 | GTCTGCTTATCCTCT[A/T]AAAGAGCACTGCTTT | 67345 |
rs51481754 | snp | A/T | | | intron-variant | Herc4 | Mm_Celera | 10:63246789 | TAAGCACAATGTAAA[A/T]TAATTTATCAGGTAA | 67345 |
rs51843647 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Herc4 | Mm_Celera | 10:63293181 | AGATCCAAGGGATTC[G/T]AACAACCCGAGCCTC | 67345 |
rs51896808 | snp | A/G | 0.32 | 0.24 | intron-variant | Herc4 | Mm_Celera | 10:63287588 | TATTAGGTAAGTGGC[A/G]GTTCCTTGATTGACT | 67345 |
rs51928078 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63261218 | AATGAATGAATTAGG[A/G]AAGTTATTTCTTTTT | 67345 |
rs52531349 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63293615 | ATCACATGACAGACA[G/T]TTATTTATTTATTTA | 67345 |
rs52635531 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Herc4 | GRCm38.p3 | 10:63295541 | GATTGCTCTTCTGAG[C/T]CAGACATGGTTCACA | 67345 |
rs52645926 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Herc4 | Mm_Celera | 10:63260224 | ATGTTGGTCTAAATA[C/T]CCCCAGACAGACTCT | 67345 |
rs52683137 | snp | G/T | | | intron-variant | Herc4 | Mm_Celera | 10:63247074 | TTGGTTTTCTTTTTG[G/T]TTTTTTTTGGGTTTT | 67345 |
rs211700879 | snp | C/T | | | intron-variant | Herc4 | Mm_Celera | 10:63248870 | CACCCTTTTATTATA[C/T]TAAGAGTGTGGGTTA | 67345 |
rs211706527 | snp | C/T | | | intron-variant | Herc4 | Mm_Celera | 10:63251141 | TTGGGTGAGATTGTG[C/T]AGGATAAGGATCAGT | 67345 |
rs211763746 | snp | A/C | | | intron-variant | Herc4 | Mm_Celera | 10:63247609 | GAAGTATAACTTAAA[A/C]CGCAGGGATGTGTTT | 67345 |
rs211764105 | in-del | -/A | | | intron-variant | Herc4 | Mm_Celera | 10:63274632 | GTTTTTATTCTGCAT[-/A]AAAAATATACTCATG | 67345 |
rs211765176 | snp | A/C | | | intron-variant | Herc4 | Mm_Celera | 10:63258216 | TATATATATAGCTAG[A/C]GAGAGAGAGAGAGAG | 67345 |
rs211765289 | in-del | -/T | | | intron-variant | Herc4 | Mm_Celera | 10:63262545 | ACGTTCTTATTAATC[-/T]TTTTTTTTTCTTCCC | 67345 |
rs211798289 | in-del | -/TAC | | | intron-variant | Herc4 | Mm_Celera | 10:63286561 | TTTAATCCCAGCACT[-/TAC]GAGTCAGAACCAGGT | 67345 |
rs211828769 | snp | C/G | | | intron-variant | Herc4 | Mm_Celera | 10:63297337 | AAAAAAATTATCTAT[C/G]TATCTAATGTATATG | 67345 |
rs211842396 | snp | A/C | | | upstream-variant-2KB | Herc4 | Mm_Celera | 10:63242439 | tttctgagttcgagg[A/C]cagcctggtctgcaa | 67345 |
rs211877217 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63257279 | AGTGTGCATGTGCAG[A/G]TTTACATGGAGAGGT | 67345 |
rs211929321 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63267224 | GTAGAGCTTATTTGA[A/G]AGATAGTGCTTGTTG | 67345 |
rs211948299 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63278246 | AAACACTGAGTCTGT[A/G]TCAAAAGTGAACTCA | 67345 |
rs211958835 | snp | C/T | | | intron-variant | Herc4 | Mm_Celera | 10:63268561 | TGGTGTGGGTGGTAC[C/T]CACCAGCAGGAGCAG | 67345 |
rs211996301 | snp | C/G | | | intron-variant | Herc4 | Mm_Celera | 10:63291753 | CACGTGGTAGCAGGG[C/G]TCTCTGCCTCTCTGC | 67345 |
rs212110990 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63293868 | TGTGCATTCCACCGT[A/G]TATGGAACACTGGCT | 67345 |
rs212117237 | in-del | -/CTTTC | | | intron-variant | Herc4 | Mm_Celera | 10:63297029 | TTACAGGAGTCAGTT[-/CTTTC]CTTTCACCTTATGGA | 67345 |
rs212139949 | snp | A/C | | | intron-variant, downstream-variant-500B | Herc4 | Mm_Celera | 10:63290811 | TATTCATAGTTTCTC[A/C]TAATTTCCTTTACAA | 67345 |
rs212141252 | snp | G/T | | | intron-variant | Herc4 | Mm_Celera | 10:63277702 | AAGTACCTGAGATGC[G/T]GAAGCAGGAGGACCT | 67345 |
rs212141526 | snp | A/G | | | intron-variant | Herc4 | Mm_Celera | 10:63300626 | GTGATTCAGTTTCCC[A/G]GTGCTGGGATTATAG | 67345 |
rs212156595 | in-del | -/G | | | intron-variant | Herc4 | Mm_Celera | 10:63251525 | CATAGGGTCAGCTCT[-/G]GGGTGCACACAGAAA | 67345 |
rs212168736 | snp | C/T | | | intron-variant | Herc4 | Mm_Celera | 10:63308714 | TAGCATTAGAGATCA[C/T]TGACCGCTTGTAATT | 67345 |
rs212173792 | snp | C/T | | | intron-variant, downstream-variant-500B | Herc4 | Mm_Celera | 10:63299567 | TGCTTTAAACCCAGG[C/T]GAGAATCCCAGAACC | 67345 |