SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6160674 | snp | A/G | 0.456747 | 0.140554 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59499048 | TTTTCGGGTGTTCCT[A/G]TAGTNGAGAAGCAGA | 68501 |
rs6160690 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Nsmce2 | Mm_Celera | 15:59499053 | GGGTGTTCCTNTAGT[C/G]GAGAAGCAGAGTGTC | 68501 |
rs6165351 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | Mm_Celera | 15:59390806 | aaggactaaaacaga[C/T]aaaaagaagaaaaaa | 68501 |
rs6167065 | snp | A/G | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59391128 | TTCCCCGTTACAGAC[A/G]AAGTCCTGTATTCAT | 68501 |
rs6173896 | snp | C/T | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59499115 | CCTCTATAAACACTG[C/T]ACTGGAGAAGACTTT | 68501 |
rs6188558 | snp | A/G | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59467850 | agaaaagaaaagaaa[A/G]gaaaaTGTTTACTAT | 68501 |
rs6210050 | snp | A/T | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59436378 | accacccataatgag[A/T]tctgacgccctcttc | 68501 |
rs6210092 | snp | C/T | 0.5 | 0 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59436401 | ccctcttctggtgtg[C/T]ctgaagtcagctaca | 68501 |
rs6210588 | snp | A/G | 0.49827 | 0.0293608 | intron-variant | Nsmce2 | Mm_Celera | 15:59436472 | GCGAGCAGGAACTGA[A/G]TTAGTGGAGTTGACT | 68501 |
rs6210656 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Nsmce2 | Mm_Celera | 15:59436504 | GAGCCAGTGGGGCAG[C/T]TGACTGGAGCAAAca | 68501 |
rs6248932 | snp | C/T | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59477502 | CCTATATCACAAGTT[C/T]GTGCATTAATAAGGC | 68501 |
rs6249481 | snp | G/T | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59477611 | ATGTGAATCATTCAC[G/T]CGTGACTATTGGGCT | 68501 |
rs6264174 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Nsmce2 | Mm_Celera | 15:59478055 | TTTCATCCACATGTT[C/T]TTTTAAGCACCTGTG | 68501 |
rs6265788 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Nsmce2 | Mm_Celera | 15:59478382 | CCCTTTGGCTGTTCT[A/C]CACACTTGTTCTACA | 68501 |
rs6266263 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59478437 | GGGTGTGCTGACCAG[C/G]TCTTGCCCACTTCGT | 68501 |
rs6266376 | snp | C/T | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59478500 | AAGATAAGGAACACT[C/T]GTCCTGCGTCTTGGG | 68501 |
rs6354664 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Nsmce2, E430025E21Rik | Mm_Celera | 15:59374826 | AGCATGAAGGAATGG[C/T]AGAAGTCGGCAATTA | 68501 |
rs6354684 | snp | A/G | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Nsmce2, E430025E21Rik | Mm_Celera | 15:59374847 | TCGGCAATTAGCCGT[A/G]TTAAGTTATATAGTA | 68501 |
rs6355285 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Nsmce2, E430025E21Rik | Mm_Celera | 15:59374977 | CACTTCAACTCTTGT[C/T]GTATGAGATCACCTT | 68501 |
rs6402340 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Nsmce2 | Mm_Celera | 15:59453025 | AAGCAGCTAGAACCT[A/G]CGGGTGAAGAATAGG | 68501 |
rs31582830 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59437694 | GGCCGAGCAACAGCC[A/G]AGAGCTCTTGGAGCA | 68501 |
rs31608876 | snp | A/G | 0.5 | 0 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59434607 | CATTAGACACAGTGA[A/G]CACTATTGGCTCTGC | 68501 |
rs31664510 | snp | A/C | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Nsmce2, E430025E21Rik | Mm_Celera | 15:59375746 | TAGCTAGTCACCTCG[A/C]CAAAGGCCTTATCTT | 68501 |
rs31701827 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59560325 | GTGCATGTACACACA[C/T]GCACACACACAGACT | 68501 |
rs31731916 | snp | A/C | 0.5 | 0 | intron-variant | Nsmce2 | Mm_Celera | 15:59445225 | CCTCCGCCCCCCCCC[A/C]CACACACACCCCTCC | 68501 |
rs31746466 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59495100 | TTCTTTTCTTTTCTT[C/T]CTTCCTTCCTTCCTT | 68501 |
rs31776037 | snp | C/G | 0.455 | 0.143091 | intron-variant | Nsmce2 | Mm_Celera | 15:59425300 | TGATTTGTTTCTTCT[C/G]TAGGAACATTGCCCT | 68501 |
rs31809089 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Nsmce2 | Mm_Celera | 15:59529631 | CAGGATGCCCTGTTT[C/T]GATTTGACATTCCAG | 68501 |
rs31890358 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59442648 | ATTTGTAGCCAAAGC[C/T]TACTGCTTTCTTCAA | 68501 |
rs31921911 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59378637 | GAGTTGAAGCATCAG[A/G]AAAAAGGGTATTCTT | 68501 |
rs32042728 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | Mm_Celera | 15:59436798 | AGTTGCTGGGTAGGT[C/T]GGTCGCTCAGGTGGG | 68501 |
rs32043424 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Nsmce2 | Mm_Celera | 15:59448026 | TTTATTTACCTAACT[A/G]GTCATCTGAAAGTCA | 68501 |
rs32055509 | snp | A/C | 0.265928 | 0.249492 | intron-variant | Nsmce2 | Mm_Celera | 15:59574511 | GAAGTCCTGTGTCGT[A/C]CTGTGCATGTGAGGA | 68501 |
rs32055723 | snp | A/G | 0.207612 | 0.24638 | intron-variant, upstream-variant-2KB | Nsmce2, E430025E21Rik | Mm_Celera | 15:59374806 | TTCCAGTTTAAGGAG[A/G]TCCCAGCATGAAGGA | 68501 |
rs32107264 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59495096 | TCTTTTCTTTTCTTT[C/T]CTTTCTTCCTTCCTT | 68501 |
rs32108279 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59381143 | TGAAGACAGCTACAG[C/T]GTGCTTACATAAAAT | 68501 |
rs32127320 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nsmce2 | Mm_Celera | 15:59521006 | AGGACCTGAGTTGGG[C/T]TCCCAGCACACAGGT | 68501 |
rs32132911 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Nsmce2 | Mm_Celera | 15:59398116 | CCAGCAACCATGTGG[A/T]ACCCTGGAGTTGGTG | 68501 |
rs32329723 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59534154 | GCCAGGGTCTGCCAC[C/T]TAGTGACTCACCTTG | 68501 |
rs32346899 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59378400 | AAACAGTTTTTTTTT[C/T]TTTTTTAAGACTTCA | 68501 |
rs32348178 | snp | C/T | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59378402 | ACAGTTTTTTTTTCT[C/T]TTTTAAGACTTCAAA | 68501 |
rs32358761 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | Mm_Celera | 15:59548142 | CTCTCTCTCTCTCTC[A/T]CACACACACACACAC | 68501 |
rs32404866 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | Mm_Celera | 15:59561939 | ACACACACACACACA[C/T]ATATATATATATATA | 68501 |
rs32417561 | snp | C/G | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59402704 | AGGGTTTTTTAAGTT[C/G]TTCTTCTTCTTATTT | 68501 |
rs32439536 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | Mm_Celera | 15:59594701 | ATTTTTTAAAAAAAT[G/T]TTGCTTGTTATTGTA | 68501 |
rs32441080 | snp | A/G | 0.375 | 0.216506 | intron-variant | Nsmce2 | Mm_Celera | 15:59425739 | CTTGCTCTGTAATAC[A/G]AATTAATTGGGATGT | 68501 |
rs32467972 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59548188 | CACACACACACACAC[A/T]CTCTCTCTCTCTCTC | 68501 |
rs36239962 | snp | G/T | 0.32 | 0.24 | intron-variant | Nsmce2 | Mm_Celera | 15:59467934 | CAGCTCATGGCTAAG[G/T]CCAGTAACCACCAGA | 68501 |
rs36242116 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59456328 | TTTCCCTTTCAAACG[C/T]TAGCCTTCTTTCACA | 68501 |
rs36242588 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59555358 | ATCTGGGTATGTAAG[A/G]TAGGCATAGGAACTA | 68501 |
rs36243182 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Nsmce2 | Mm_Celera | 15:59418635 | AAGACTTTCAGAATG[A/C]GTGAGTTTAATGCCT | 68501 |
rs36245484 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59466300 | CTCACAAGGAGGAGA[A/G]AAGTTTTAGAAGGTG | 68501 |
rs36245635 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59532805 | CTCTACCTTCTAGCT[A/T]TTAATGAATAACGAG | 68501 |
rs36250313 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59517634 | ATAAAAAAGCTGGAT[A/G]TGGTGACTCAGTGAC | 68501 |
rs36253646 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Nsmce2 | Mm_Celera | 15:59478887 | AAAAGTCCTATGTGT[G/T]TTGGGAATCGAAATA | 68501 |
rs36255218 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Nsmce2 | Mm_Celera | 15:59391766 | CTGGTGAGTCTTCCA[A/G]TCAAACCGGTGGAAG | 68501 |
rs36257396 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59528410 | ATTGTGCCCTCTAGA[C/T]TCTGCTTGGTGATCT | 68501 |
rs36258118 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Nsmce2 | Mm_Celera | 15:59402312 | TTTGATAGTACATAT[A/G]CTAAAGTCCTGCTGT | 68501 |
rs36263139 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Nsmce2, E430025E21Rik | Mm_Celera | 15:59374946 | GAGAAGGGTGTATGC[A/G]TGCTGAAAACGGAGA | 68501 |
rs36264352 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59514893 | AAACCCATTAGCATC[A/G]TTGTTATCTGTTTTA | 68501 |
rs36266146 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59498507 | CTGGGTTTCTGAATT[A/C]TTTTTTGGCATCTGT | 68501 |
rs36266639 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59572725 | TAATTTAGAATTAGA[A/G]CAAGATGATAAAATT | 68501 |
rs36268891 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59454771 | CGAGTGGTAACTGCA[A/G]CAGTGATGACATACA | 68501 |
rs36269770 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Nsmce2 | Mm_Celera | 15:59392880 | TTGGGAGTGAGAAGA[G/T]AATGGTATTCAAGAA | 68501 |
rs36271414 | snp | A/G | 0.32 | 0.24 | intron-variant | Nsmce2 | Mm_Celera | 15:59426688 | CCTGATTTTACAAAG[A/G]AAATTTGTATTGTCT | 68501 |
rs36272495 | snp | C/G | 0.32 | 0.24 | intron-variant | Nsmce2 | Mm_Celera | 15:59496938 | AAGGGATTAAGTTCT[C/G]TGTGTCCTTCTAGAT | 68501 |
rs36274359 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59570417 | AAATACCCACAAAAA[A/C]TTTTGTCTGCTTTTT | 68501 |
rs36277836 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nsmce2 | Mm_Celera | 15:59393078 | GGCCTCGTTAATATG[C/T]GACTTGAGCTAGATG | 68501 |
rs36277895 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nsmce2 | Mm_Celera | 15:59510693 | AGAATTCCCTGCTGC[C/T]CGTGTATTTCCAGGC | 68501 |
rs36278219 | snp | A/T | 0.32 | 0.24 | intron-variant | Nsmce2 | Mm_Celera | 15:59568337 | GCATTCTCATGGGTC[A/T]TACTGACATGACTAG | 68501 |
rs36280515 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59458200 | AGGTGGTTGAGTCTG[A/G]TGGACAGTGTTCTCC | 68501 |
rs36280743 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Nsmce2 | Mm_Celera | 15:59504095 | CCAGTGTTTAAAGAC[A/G]TACTGAAGGAAGCCT | 68501 |
rs36281134 | snp | A/G/T | 0.124444 | 0.216185 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59430390 | GTACGAACGACCCAC[A/G/T]TTTACTTTTTGCCTT | 68501 |
rs36281811 | snp | C/T | 0.32 | 0.24 | intron-variant | Nsmce2 | Mm_Celera | 15:59418755 | ACCTGTCATCATCAC[C/T]GTTTACTGCCTTTGA | 68501 |
rs36282704 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59438028 | TCTTCTGGTTAAGAC[C/T]TCTTGACTTGTAAGG | 68501 |
rs36282804 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59548270 | CACACACGCTTGTGC[A/G]TTAGAGACACACAGC | 68501 |
rs36289860 | snp | G/T | 0.459184 | 0.136902 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59499319 | AGAATGTAAATCGTG[G/T]TGTGAGCTGGAGACT | 68501 |
rs36289989 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59431281 | CTTTCTGTTAAGCAT[G/T]GAAAGAGCTCATTGG | 68501 |
rs36290534 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59430605 | AGTTAAAACAGTTTA[C/T]ACTCTCTGATCAGAT | 68501 |
rs36290747 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59448487 | AATAAGTAAGTGAGC[A/T]CATTGTATGTCCCTT | 68501 |
rs36292634 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Nsmce2 | Mm_Celera | 15:59392927 | CAGTTGTCTTTAGGA[C/T]AGGGTATTTATTAAC | 68501 |
rs36293886 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Nsmce2 | Mm_Celera | 15:59425139 | GATCGAAGAGAGAAG[A/C]AGGTAAGAAGCTATT | 68501 |
rs36297516 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Nsmce2 | Mm_Celera | 15:59382124 | TTCGGTCACCTGTGA[C/T]CTCTTAAGTGTCTTA | 68501 |
rs36298122 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmce2 | Mm_Celera | 15:59485967 | TGGCAGAGCACAGAA[A/G]GCCGGAGTGCCGCAG | 68501 |
rs36300632 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59530361 | TTTAGCATTGTCTGG[C/T]ATACAGTGGGTATCA | 68501 |
rs36301494 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59447800 | CGGGTCTCAGTGCCT[A/G]TTTGTTGAAGGAGTG | 68501 |
rs36301623 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Nsmce2 | Mm_Celera | 15:59516859 | GTACCTTTCCTTTTT[C/T]GCTTCATCTGTGGCA | 68501 |
rs36302267 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59571179 | AATGGGGTTTTAGAT[G/T]AATTTTACTCCAGCA | 68501 |
rs36303191 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Nsmce2 | Mm_Celera | 15:59559650 | AGTTGGTCGCTACAG[A/T]GGAATTACATTTGAA | 68501 |
rs36305586 | snp | A/T | 0.486111 | 0.0821678 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59535349 | GAGCTTGGAGAAATA[A/T]ATAGTCAGGACCCTG | 68501 |
rs36306484 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Nsmce2 | Mm_Celera | 15:59541418 | CTGCTGAAAGATAGC[A/G]TATTTTATAAATAAC | 68501 |
rs36306704 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59379251 | AAAGCTGTGAACACA[G/T]ATATTGTGGTTCCTT | 68501 |
rs36307177 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59435740 | AGCGGAGCCTAGCCT[A/G]GCTGACGTTCCTCCA | 68501 |
rs36308978 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Nsmce2 | Mm_Celera | 15:59571496 | TGGCACCTGGTACCC[A/G]GCTGCTGTGGAGTCT | 68501 |
rs36309626 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | GRCm38.p3 | 15:59450062 | GCAAATAGCAGCTCT[C/T]TTACATCAATTTGCA | 68501 |
rs36309668 | snp | C/T | 0.32 | 0.24 | intron-variant | Nsmce2 | Mm_Celera | 15:59535965 | GTATGTATCTCTGCG[C/T]TGTGGAGGTCCCAGT | 68501 |
rs36311548 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Nsmce2 | Mm_Celera | 15:59429138 | CTGCTGGCAAAGGTG[C/G]TACTTTTTCTTTTGT | 68501 |
rs36313673 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Nsmce2 | Mm_Celera | 15:59378058 | TCTGATTTCAAAAGA[C/T]CATTCTCCTTTATGG | 68501 |
rs36317418 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | Mm_Celera | 15:59565344 | CTGTCCCCAGGTCCT[C/T]ACTCGTGGCATATGG | 68501 |
rs36318178 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Nsmce2 | Mm_Celera | 15:59399127 | TTGAAAAGATGGATC[C/T]TGTAGAGCCTTAGGG | 68501 |