SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6178003 | snp | A/T | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95461592 | GCACTCCCAAGATAA[A/T]CTCTGCCCTGTATTG | 20747 |
rs6178035 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Spop | GRCm38.p3 | 11:95461626 | GAATCAGGCAGGCAG[A/T]GGACCCTCAAGACAA | 20747 |
rs6178081 | snp | A/G | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95461652 | GACAACCCTCACCTC[A/G]TGCCTTGNAGCCCAA | 20747 |
rs6178459 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Spop | GRCm38.p3 | 11:95461660 | TCACCTCNTGCCTTG[C/T]AGCCCAAGCACCCTG | 20747 |
rs6180054 | snp | C/G | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95462011 | tccctggtctaagct[C/G]tccctgcatcttgcc | 20747 |
rs6266010 | snp | A/G | 0.5 | 0 | intron-variant | Spop | Mm_Celera | 11:95439829 | tgagactgaggtcaa[A/G]ccagtctacaaagtt | 20747 |
rs6266680 | snp | C/G | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95439975 | cctagcaaccacatg[C/G]tggctcacaaccatc | 20747 |
rs6267752 | snp | G/T | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95440135 | ATAGTATGCTACAGT[G/T]GAAATATCATGAATG | 20747 |
rs6268319 | snp | G/T | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95440244 | agacatggctcagca[G/T]ttaagaccactgact | 20747 |
rs6268365 | snp | A/G | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95440273 | ctgctcttcctagag[A/G]tcctgagttcaattc | 20747 |
rs6281150 | snp | C/G | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95440359 | tggtgtgtctgaaga[C/G]agtgacacacatgtg | 20747 |
rs6281683 | snp | G/T | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95440446 | ACTCCTTTTCTTCAT[G/T]CATATAAGCTCTTAG | 20747 |
rs6281737 | snp | A/G | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95440471 | TCTTAGGAGTGTCTG[A/G]TGTTTACATTTTTTT | 20747 |
rs6282225 | snp | C/T | 0.5 | 0 | intron-variant | Spop | Mm_Celera | 11:95440552 | AATAGATGCTATTAA[C/T]TAAATCAGTTATAGC | 20747 |
rs27087609 | snp | A/C/T | 0.197531 | 0.244432 | utr-variant-3-prime | Spop | GRCm38.p3 | 11:95493147 | AGAATGTCTAAGAAG[A/C/T]GGTAGGATTTATTTA | 20747 |
rs27087610 | snp | C/G | 0.277778 | 0.248452 | utr-variant-3-prime | Spop | GRCm38.p3 | 11:95491966 | GGGAAAAGACTGCAC[C/G]ATGACCCAGACTTTA | 20747 |
rs27087611 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Spop | Mm_Celera | 11:95490539 | CCTTTCGATGGGAAA[C/T]AGAGAATTGTTATCT | 20747 |
rs27087612 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Spop | Mm_Celera | 11:95489998 | AGTGCTTCATTGTCA[A/G]GGTAGGTGGAGACTG | 20747 |
rs27087613 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Spop | Mm_Celera | 11:95488057 | TTATACACCTCAGGT[C/T]TGTATCCTCTTATCT | 20747 |
rs27087614 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Spop | Mm_Celera | 11:95487270 | CAATGGGAACTGGCT[G/T]GCATTGTAAAGCCAC | 20747 |
rs27087615 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Spop | Mm_Celera | 11:95486137 | TGCTCAAAATGGTAA[A/G]CTCTCAGGGTCAACT | 20747 |
rs27087616 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95486109 | GTAGTAACGTTTGGT[A/G]CTAAAAGTGTCCTGC | 20747 |
rs27087617 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Spop | Mm_Celera | 11:95486084 | CATTCTTACACATTA[C/T]TCTAACACAGTAGTA | 20747 |
rs27087618 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Spop | GRCm38.p3 | 11:95486036 | TGTGTGTAGGTGAAG[C/T]GAACATACATATATC | 20747 |
rs27087619 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Spop | Mm_Celera | 11:95485831 | CTCTCAGCTTTTCCG[G/T]CGTAGAATCGGGTTG | 20747 |
rs27087620 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spop | Mm_Celera | 11:95485809 | CTGTCTGTTAGGACG[C/T]TCCTCACTCTCAGCT | 20747 |
rs27087621 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spop | Mm_Celera | 11:95485807 | TTCTGTCTGTTAGGA[C/T]GCTCCTCACTCTCAG | 20747 |
rs27087622 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95485042 | CCAACTTCAACAATG[A/G]AATACCTTCCTTCCA | 20747 |
rs27087623 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Spop | GRCm38.p3 | 11:95484482 | TAAACTACATACAGG[C/T]CCAAAGCTCCAGGTC | 20747 |
rs27087624 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95484444 | ATAGAAAATGACAGG[A/G]CTAAAATGAGTTCTT | 20747 |
rs27087625 | snp | C/T | 0.375 | 0.216506 | intron-variant | Spop | GRCm38.p3 | 11:95484026 | TCCCTCTCTCTCCCT[C/T]GCCTGTCCCTTCAGA | 20747 |
rs27087626 | snp | A/G | 0.375 | 0.216506 | intron-variant | Spop | GRCm38.p3 | 11:95483482 | ACAGTAGATATTTCA[A/G]ACTTCAGCCTTTCCC | 20747 |
rs27087627 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Spop | GRCm38.p3 | 11:95482983 | CTTTCCATTCTCTGC[C/T]TCAGCTTGGTATTGT | 20747 |
rs27087628 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Spop | GRCm38.p3 | 11:95482954 | AGATGAGCTCAGCCT[A/G]TCTCATGTGACAACT | 20747 |
rs27087629 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spop | Mm_Celera | 11:95482852 | TAGAGCGTGGAATAG[C/T]ATCGAGTGACTCTCC | 20747 |
rs27087630 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Spop | Mm_Celera | 11:95482775 | CCGAGGAAGAACTGA[G/T]AGAGGGCTGACTTCG | 20747 |
rs27087631 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95482707 | GCTACTGACCCAGAG[C/G]ATCAGCTCTTGTTCT | 20747 |
rs27087632 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Spop | Mm_Celera | 11:95482646 | AGGCCTCTCAGATGG[C/T]TAAGCCAATGCCTTC | 20747 |
rs27087633 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Spop | Mm_Celera | 11:95481889 | GGTAACAAAAGCTTT[C/G]TTTCTGTCTCTTTAT | 20747 |
rs27087634 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95480983 | CTCAGGGATTGAATT[C/T]GGCTTAGCCCTAACT | 20747 |
rs27087635 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95480885 | ATCTTGAAGGTCAAA[A/G]GAAATCTAGGTCATC | 20747 |
rs27087636 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95480547 | AAAGAAATGAGGGCA[C/T]CAATATGACAAAATG | 20747 |
rs27087637 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Spop | Mm_Celera | 11:95479224 | AGTTGTTAACAGGTA[A/C]TGAAGGTTTCTATGG | 20747 |
rs27087638 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Spop | GRCm38.p3 | 11:95478875 | TGAATGATGTGTGCT[A/G]TACTATAAACACTGT | 20747 |
rs27087639 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Spop | Mm_Celera | 11:95478699 | GGACTGTTGTCACCT[A/G]GCTAGGACCTGCTGT | 20747 |
rs27087640 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Spop | Mm_Celera | 11:95478564 | GCAACATCTTTGTAG[A/G]TTATAAACTATGTTG | 20747 |
rs27087641 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Spop | GRCm38.p3 | 11:95477675 | GTTAGCAATGGAGGT[A/G]CATGCATTTCCCCTT | 20747 |
rs27087642 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95477660 | TGAGAACAAATACTC[A/G]TTAGCAATGGAGGTA | 20747 |
rs27087643 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spop | GRCm38.p3 | 11:95477642 | CTCTCTGGTTACTTA[C/T]ACTGAGAACAAATAC | 20747 |
rs27087644 | snp | C/T | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95477360 | AGACAAGTAGTGTCT[C/T]GGGAGGTCAGGTAAT | 20747 |
rs27087645 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Spop | GRCm38.p3 | 11:95477206 | ATTTTTGTCTATTAG[A/G]AAGTATGGCGATTCT | 20747 |
rs27087646 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Spop | GRCm38.p3 | 11:95476496 | GAGTTCTGCTGATGC[C/T]GTGCTTTCTCGCCAT | 20747 |
rs27087647 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95476323 | CTTATCCTATGGTTA[A/G]GTCTGAGGCTGAGTT | 20747 |
rs27087648 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95475904 | TGTATAAACAGCATC[A/G]GCTTCAATCTTTGCC | 20747 |
rs27087649 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95475803 | GAAGTGTGAGTTTCA[C/T]GTTAGTCTTATTAGC | 20747 |
rs27087650 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Spop | GRCm38.p3 | 11:95475495 | TGAAATAACAGGCTT[A/G]CATTGTGAGTTAATG | 20747 |
rs27087651 | snp | A/T | 0.375 | 0.216506 | intron-variant | Spop | GRCm38.p3 | 11:95475464 | AGGCCAAGAGTCCCA[A/T]CTGACAGCTAGCCCA | 20747 |
rs27087652 | snp | C/T | 0.49827 | 0.0293608 | intron-variant | Spop | GRCm38.p3 | 11:95475412 | ACTGCTTCCTGAGAG[C/T]GAAACAAATAACCAG | 20747 |
rs27087653 | snp | G/T | 0.42 | 0.183303 | intron-variant | Spop | GRCm38.p3 | 11:95475338 | ACTTGGGTAAATAAG[G/T]AAAAGTTTTATCCCG | 20747 |
rs27087654 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Spop | GRCm38.p3 | 11:95475291 | ATTGCAATGAGCCAA[C/T]TTATGCCATTTTCCA | 20747 |
rs27087655 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Spop | GRCm38.p3 | 11:95475161 | GAGAGTTAGCTGTTA[C/T]CAGATTGAGAGGTCA | 20747 |
rs27087656 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spop | Mm_Celera | 11:95475064 | CTTTGTAGGAGTTGA[A/G]TGTACATGGTTTGTC | 20747 |
rs27087657 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Spop | GRCm38.p3 | 11:95475043 | TCTCCTTTTTTGCTC[C/T]CTGGACTTTGTAGGA | 20747 |
rs27087658 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95474909 | ACATAGTATTTGGAA[A/G]GTCTGATGCTTCAAG | 20747 |
rs27087659 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Spop | Mm_Celera | 11:95474897 | GTGGGTTTTTTCACA[C/T]AGTATTTGGAAGGTC | 20747 |
rs27087660 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Spop | GRCm38.p3 | 11:95474751 | AATGTTCTTTATGTG[A/G]CTGATTGAGCTGCCT | 20747 |
rs27087661 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Spop | Mm_Celera | 11:95474173 | GTTCTCATGTTCGTG[C/T]TGGGCTGCAGGAGCC | 20747 |
rs27087662 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Spop | Mm_Celera | 11:95474164 | CCCCTCTGGGTTCTC[A/G]TGTTCGTGTTGGGCT | 20747 |
rs27087663 | snp | A/G | 0.375 | 0.216506 | intron-variant | Spop | GRCm38.p3 | 11:95474115 | GGGCTTAGAGTTTAA[A/G]AAGCTAACAACAGTA | 20747 |
rs27087664 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Spop | Mm_Celera | 11:95474007 | TGTAAGGGATGTGAA[C/T]GCTCCGTGATTCTTG | 20747 |
rs27087665 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Spop | Mm_Celera | 11:95473860 | TGAAAAAAAATTATT[C/T]CTCCATCATGAAAAA | 20747 |
rs27087666 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spop | GRCm38.p3 | 11:95473040 | CTTACTGAGTGAAAT[A/G]TTTGTTCTAGGCATA | 20747 |
rs27087667 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Spop | GRCm38.p3 | 11:95472945 | ATTTTGTCTCTGAAC[C/T]ACCACTTTGATCTCT | 20747 |
rs27087668 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Spop | Mm_Celera | 11:95472899 | CAGGTGGTTAAGGCT[A/G]CAACCATATGTCCCC | 20747 |
rs27087669 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Spop | Mm_Celera | 11:95472807 | ATTCCTGAACTTAGA[A/G]CCTATTGCCAGGTGA | 20747 |
rs27087670 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Spop | GRCm38.p3 | 11:95472761 | ATAGTCAAGCGTGTG[C/T]CATTCATGTACTGAA | 20747 |
rs27087671 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Spop | GRCm38.p3 | 11:95472715 | TCTGCCACATGCCAG[C/T]AAATCTTTGAGCTTT | 20747 |
rs27087672 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95472700 | GTAACAATGTGTATA[A/T]CTGCCACATGCCAGT | 20747 |
rs27087673 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Spop | Mm_Celera | 11:95472692 | TGCTTGAAGTAACAA[C/T]GTGTATATCTGCCAC | 20747 |
rs27087674 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Spop | GRCm38.p3 | 11:95472660 | ATGGTATAAATGTCT[A/T]AAGTGTAGCTTCCCT | 20747 |
rs27087675 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Spop | Mm_Celera | 11:95472621 | TTCCAGGAGACACAT[C/T]ATTACACTGCAGACC | 20747 |
rs27087676 | snp | A/T | 0.35503 | 0.226867 | intron-variant | Spop | GRCm38.p3 | 11:95471850 | AAGTATATGAAGGAC[A/T]GGTAACAACCCAGCT | 20747 |
rs27087677 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Spop | GRCm38.p3 | 11:95471211 | AATTCCTTCCTAATT[C/T]TCTATCAACAGATCA | 20747 |
rs27087678 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Spop | Mm_Celera | 11:95471083 | AAAACAGTCGGTCAC[G/T]GAGACTTCTTTAATT | 20747 |
rs27087679 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95471070 | GGTGAAAAGTTATAA[A/C]ACAGTCGGTCACTGA | 20747 |
rs27087680 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Spop | Mm_Celera | 11:95471027 | TCCGGCACTTGGGTT[C/T]TCTCACTTCCCTCCA | 20747 |
rs27087681 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95470970 | CAGAGCTTTAGACTT[C/T]CCCTACCCTGTCCGT | 20747 |
rs27087682 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Spop | GRCm38.p3 | 11:95470954 | GGCTTGTTTAGGACC[A/C]CAGAGCTTTAGACTT | 20747 |
rs27087683 | snp | A/T | 0.497041 | 0.0383476 | intron-variant | Spop | GRCm38.p3 | 11:95470905 | CAGTGTTTGAGATCC[A/T]CAGCCCCAGGATGGC | 20747 |
rs27087684 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Spop | GRCm38.p3 | 11:95470772 | ACCTTATTGGCCTTG[C/T]TTTTCTGACATAGAA | 20747 |
rs27087685 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Spop | Mm_Celera | 11:95470744 | TGTCTCTGGCAAACA[G/T]CACAAGATGAGGACC | 20747 |
rs27087686 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Spop | GRCm38.p3 | 11:95470706 | AAGCACCACACTCAC[G/T]TTCTTGCTCTTGAGG | 20747 |
rs27087687 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Spop | Mm_Celera | 11:95470674 | TACACAGGTAAGCTC[A/G]GGAGGCTGCTGGGCA | 20747 |
rs27087688 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Spop | GRCm38.p3 | 11:95470384 | GTTAGTTTTTAAATC[A/G]GGATAAATTGTTTCA | 20747 |
rs27087689 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Spop | Mm_Celera | 11:95469724 | TATCTAGTATTAACC[C/G]TGTTATCTGTCTATC | 20747 |
rs27087690 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Spop | GRCm38.p3 | 11:95469144 | AGAGTCAGGTAAAAA[C/T]TTGACTTGGTGTTGT | 20747 |
rs27087691 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Spop | GRCm38.p3 | 11:95469060 | TTGGAGGTGAGAGAA[A/G]GAGAGCAAGGGAAGG | 20747 |
rs27087692 | snp | C/T | 0.5 | 0 | intron-variant | Spop | GRCm38.p3 | 11:95468652 | GGAAATGTTTGTATA[C/T]TGACTGAAATTTGAT | 20747 |
rs27087693 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Spop | GRCm38.p3 | 11:95468588 | CCCACACAGGTAGGT[A/G]TATAGCAGCTATTTA | 20747 |
rs27087694 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Spop | Mm_Celera | 11:95467992 | TTCTGTTGCTTTCCA[A/T]ATTTGGCAATCCCTG | 20747 |