SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3725950 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160915248 | GTTGTGGGAATTGTG[A/G]TTGCTGGGAATTGAA | 381305 |
rs6227506 | snp | C/G | 0.5 | 0 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160952371 | gttatggttgagtca[C/G]cacaacatgaggaac | 381305 |
rs6227587 | snp | G/T | 0.5 | 0 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160952417 | cagcattaggaaggt[G/T]gagagccactgCTTT | 381305 |
rs6227607 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160952436 | AGCCACTGCTTTAGA[A/G]GTTCTGTAGTCTAGG | 381305 |
rs6240669 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160952461 | TCTAGGGTCAGCTTA[A/C]TAGTAAAGTGTGTGT | 381305 |
rs6240765 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160952509 | ATCCCAGCACTCAGG[A/G]GGCAGAGGCAGAAGC | 381305 |
rs6241877 | snp | C/T | 0.5 | 0 | intron-variant | Rc3h1 | Mm_Celera | 1:160952742 | TCCTTCCCTCCCCCC[C/T]CCCTTTAGGTTACAT | 381305 |
rs6242379 | snp | A/G | 0.5 | 0 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160952821 | GCTTATTTATTGGTT[A/G]GTTAGttggttttct | 381305 |
rs13464619 | snp | A/G | | | utr-variant-3-prime | Rc3h1 | Mm_Celera | 1:160974606 | AACAAATGAGGTGGG[A/G]AAAAAAGAACTAGGA | 381305 |
rs30455060 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160908761 | AGAATCATGTGTATT[A/G]TAATGATACTGAAAT | 381305 |
rs30467565 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Rc3h1 | GRCm38.p3 | 1:160971660 | ATTCGCTTAGCCAAT[A/G]ACTTCTGTGAAGTTG | 381305 |
rs30475234 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160966457 | TTCCAGGGTTATGTT[C/T]CCCCCTTTCAGTTAT | 381305 |
rs30503031 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160962258 | ACATACTCTCATTTT[G/T]GCTTTTTGTTAGAAT | 381305 |
rs30503077 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160962113 | TAATTGTTGGTCATA[C/T]AATTCTTACTGTGAT | 381305 |
rs30511475 | snp | A/G | 0.5 | 0 | utr-variant-3-prime | Rc3h1 | Mm_Celera | 1:160969497 | ACTCTGCTGAGGTCC[A/G]CGTCACCTCAGTCTA | 381305 |
rs30511756 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160923358 | ATTTTGCTACTGTTA[C/G]GAATCATACTGTAAG | 381305 |
rs30513180 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160918439 | ACTGGAATGAGACCC[C/T]AGCACATACGCAGCA | 381305 |
rs30515068 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160964326 | GAGGATTCAGAACTA[A/G]ATTTAGTTCTTGGCT | 381305 |
rs30573473 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160920311 | GAAAAGTCCTTTTCT[A/T]TATTTAAGAGTTGTT | 381305 |
rs30603084 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Rc3h1 | Mm_Celera | 1:160961511 | CAAGGTCCTGGGCTC[C/T]GCTCCCAGCATCAAG | 381305 |
rs30608725 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160919169 | TTGAGAATTAAGTTA[C/G]ATAGTATATGTAATA | 381305 |
rs30620970 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rc3h1 | Mm_Celera | 1:160934058 | ATGACATCCTTTCTT[C/T]CAAACTGTCTTAAGT | 381305 |
rs30656926 | snp | A/C | 0.5 | 0 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160921840 | GGCTACATAGAAAAA[A/C]CTTGTCTTGAAAATA | 381305 |
rs30661506 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160921588 | GCGGACTTCTGAGTT[C/T]GAGGCCAGCATGATC | 381305 |
rs30691865 | snp | C/T | 0.32 | 0.24 | intron-variant | Rc3h1 | Mm_Celera | 1:160931959 | TTCAATTAACTACTG[C/T]TGTGTTAAATTCTGG | 381305 |
rs30701818 | snp | A/T | 0.5 | 0 | intron-variant | Rc3h1 | Mm_Celera | 1:160928037 | TAGGAGTTTTTTTTT[A/T]ATCATATGTTTTAAC | 381305 |
rs30703960 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160910967 | TTGTTTCTTAATTCA[C/T]ACAGAAATCTTGAGA | 381305 |
rs30714346 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160935851 | TACTAAGCCATCGCT[C/T]CAGCCCCCAGCTGTT | 381305 |
rs30747579 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160935615 | AGTAACGTGCCCCCC[A/C]CCCCCCCGTGCGCGC | 381305 |
rs30791367 | snp | A/C | 0.188366 | 0.242283 | intron-variant | Rc3h1 | Mm_Celera | 1:160934285 | TTGGATGACAATTTG[A/C]GGGTCTATTGGCTGT | 381305 |
rs30800697 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160921094 | AAGGTGTGAATTTGA[A/G]GCTAGCCTAAGCTAC | 381305 |
rs30802364 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160955608 | ATCTTGGGAGAGTTT[A/G]GGTTGACCTTTTTTT | 381305 |
rs30808685 | snp | A/G | 0.5 | 0 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160922739 | TTACATGTAAGTAAC[A/G]CTGTAGCTGTCTTCA | 381305 |
rs30850116 | snp | A/G | 0.32 | 0.24 | intron-variant | Rc3h1 | Mm_Celera | 1:160922075 | ATGTTGCTTTGCAAA[A/G]GACTCAAGTTTAGTT | 381305 |
rs30887367 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160920331 | TAAGAGTTGTTACAT[G/T]CCAGGCAGTGGTGGC | 381305 |
rs30915504 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160938582 | GCAAGTGTTCTACTA[C/T]TATACAGTAGTAGAT | 381305 |
rs30984302 | snp | C/T | 0.32 | 0.24 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160910710 | CTTAGTCTCTGTCTG[C/T]CTGCCTGCCTATCTT | 381305 |
rs31027286 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rc3h1 | GRCm38.p3 | 1:160905067 | GCCCGTGAACGTGCT[C/G]CAGGCCACCCTGGTC | 381305 |
rs31030007 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160911333 | TATAGACTCTTAAGA[A/G]TATCATTAAACGCCA | 381305 |
rs31128092 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160964647 | CTGGCAGCCATAGGC[A/T]TCTGCATTTCTGTTT | 381305 |
rs31134250 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Rc3h1 | Mm_Celera | 1:160945958 | GGCAGGTTAGCTGAT[A/G]GGTGAGACCATTATT | 381305 |
rs31143373 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rc3h1 | GRCm38.p3 | 1:160904905 | GCAGTGGTGACACAG[A/G]CCTTTAATCCCAGCA | 381305 |
rs31159016 | snp | C/G | 0.5 | 0 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160909345 | GAGGCCCTGCCTCAA[C/G]GAAACAAACAAACAA | 381305 |
rs31161439 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160964586 | AAGTTTGGTTCCTGT[C/T]TTACAACTGCCTGTA | 381305 |
rs31172098 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160926620 | TTCTTCATGTGGATG[C/T]TCAGTTGTCTCAGCA | 381305 |
rs31181775 | snp | G/T | 0.32 | 0.24 | intron-variant | Rc3h1 | Mm_Celera | 1:160961857 | TAAAAAAGGGGGGGG[G/T]TATCACACTGAAGTA | 381305 |
rs31186022 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160939723 | AATTACTTGTTTGTT[A/T]ATTTTGATGTTTTGA | 381305 |
rs31190259 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160933937 | GTAAATTAGCACACA[C/T]GATTGGATATTCAAG | 381305 |
rs31206611 | snp | G/T | 0.48 | 0.0979796 | utr-variant-3-prime | Rc3h1 | GRCm38.p3 | 1:160968572 | TTTAAATGAAGATTA[G/T]TTTATTTTAAGAATG | 381305 |
rs31236905 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160946727 | CTGCTTGGTTCTTCA[A/G]TTATCTTTTGTTATG | 381305 |
rs31279718 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160965912 | TTTAAAAAAATAAGA[A/G]AATATGAATATATTC | 381305 |
rs31281187 | snp | A/T | 0.188366 | 0.242283 | intron-variant | Rc3h1 | Mm_Celera | 1:160933302 | AAAAATAGCCTAAAC[A/T]TCAGAACTGATTCAC | 381305 |
rs31297123 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rc3h1 | Mm_Celera | 1:160948989 | TTTCTACTTATTTGT[A/G]TATATGCGTAGAGAT | 381305 |
rs31309174 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160938670 | TTTATTCATTATAAG[A/C]TGTACTGGCTAGCTT | 381305 |
rs31317184 | snp | A/C | 0.492188 | 0.0620098 | utr-variant-3-prime | Rc3h1 | Mm_Celera | 1:160968507 | AGCATTCCTTGCATT[A/C]TCTCCTTCAAATCTG | 381305 |
rs31335711 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160919607 | CAAAGATGATTCTTA[A/G]TGCTTCTGTCATAAG | 381305 |
rs31336949 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160919840 | CAACAACAACAACAA[A/C]AACAAAAACAACCCA | 381305 |
rs31337129 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160920893 | ACTATTTATCAATCT[A/G]AAACATCAACTGTTT | 381305 |
rs31373822 | snp | A/C | 0.188366 | 0.242283 | intron-variant | Rc3h1 | Mm_Celera | 1:160932971 | TGATTAATCCTACCG[A/C]TAATCAGGAAAATAG | 381305 |
rs31387343 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160911535 | AGTCTACTCCTCCTA[C/T]CTTCATCTGATCCAC | 381305 |
rs31417743 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160911860 | AATGAAAACTGGGGT[A/G]TGGGTTTGGGAAACT | 381305 |
rs31417813 | snp | C/T | 0.5 | 0 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160931887 | AGACTCTTCAGGTTT[C/T]CTGTAAGTGTAAAAT | 381305 |
rs31420841 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160923662 | TGCGCTCTTCTGGCA[C/T]GTAGGTATACATGAA | 381305 |
rs31428285 | snp | C/T | 0.32 | 0.24 | intron-variant | Rc3h1 | Mm_Celera | 1:160907515 | TTGTTAAGGTTTGAG[C/T]GGAACTTTTCTAACT | 381305 |
rs31447157 | snp | G/T | 0.5 | 0 | intron-variant | Rc3h1 | Mm_Celera | 1:160933038 | TTTTGTTTTGTTTTG[G/T]TTTGTTTTGGTTTTG | 381305 |
rs31472788 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160952608 | AAACAAAAGATTAAA[A/G]GGAATACTGATATTT | 381305 |
rs31476565 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160913041 | TTGAGTTTTATTTTG[A/G]AATTTATTGTTTGAT | 381305 |
rs31477441 | snp | A/G | 0.444444 | 0.157135 | utr-variant-3-prime | Rc3h1 | GRCm38.p3 | 1:160969923 | GGAGGTAGAGGCACC[A/G]AATGACGGTGAGGCA | 381305 |
rs31485245 | snp | C/T | 0.32 | 0.24 | intron-variant | Rc3h1 | Mm_Celera | 1:160951322 | ACTGGAATGGCAGAC[C/T]AGCAGCACCATGCCC | 381305 |
rs31526269 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160964751 | CATCTTTTAAAACTC[A/T]CTCTCCCTTAAAAAT | 381305 |
rs31527458 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160915572 | TGTGCCAAAAGTCTA[G/T]GTGACAGCCATTCTG | 381305 |
rs31535206 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160919171 | GAGAATTAAGTTACA[A/T]AGTATATGTAATACA | 381305 |
rs31547656 | snp | G/T | 0.5 | 0 | intron-variant | Rc3h1 | Mm_Celera | 1:160933028 | GTTTCTGTTTTTTTT[G/T]TTTTGTTTTGTTTTG | 381305 |
rs31571744 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160967186 | GGGCTGTAGGGGGGA[A/G]GAGTCTCACTACCTG | 381305 |
rs31573539 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160909571 | ACCTACATCTTCTGA[C/T]ACAAAGTAGCTGCTT | 381305 |
rs31575485 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160945201 | GGAGCCTCATAGTCT[A/G]TCTCTCATAAGCTGG | 381305 |
rs31590895 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160961803 | GATGTCTGAAGACAG[A/C]TACAGTGTACTTACA | 381305 |
rs31599984 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160954022 | CATGGTGGCTCACAA[C/T]CATCTGTAATGAAAT | 381305 |
rs31619267 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rc3h1 | Mm_Celera | 1:160934133 | GGTTGAGAACATTTC[C/T]TAGGCTTCAACCTTT | 381305 |
rs31623207 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Rc3h1 | Mm_Celera | 1:160955225 | ATTGGTGTGTGAGAG[C/T]GAGCACAGGTACATG | 381305 |
rs31649257 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160932588 | GAGATCCCATCAAAA[A/G]TCAGTATACAACACG | 381305 |
rs31664822 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rc3h1 | Mm_Celera | 1:160916480 | TAATTCTGCCAAACC[A/G]GGAGCATGGAATGTC | 381305 |
rs31666074 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160935687 | TTAATTTTTTTAAAC[A/T]TGTATTTTATTTATA | 381305 |
rs31683891 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160950618 | ATAAAAGGAATAATT[A/G]AATTCAACACTTAGG | 381305 |
rs31688138 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160924415 | TATCTATAAACAGGT[A/G]TACTTCTGTCAGGAG | 381305 |
rs31694027 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160938047 | ACTATAAGTGGGTAA[C/G]TTGTACTCAGCAAAA | 381305 |
rs31710416 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rc3h1 | Mm_Celera | 1:160924788 | ATTATCTGGTTTTAG[A/G]TTTCCTGTCACTTAA | 381305 |
rs31717229 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160945315 | TCACAGCACGTCTTC[C/T]CATTCTCCAGCTTTT | 381305 |
rs31726450 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160938391 | TACTTTCAAGTGCTA[A/G]AATTAAAGGTGTGCC | 381305 |
rs31731404 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160944451 | ATAATTTTACATAGA[A/G]TAAATATTACCTCTC | 381305 |
rs31749610 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rc3h1 | Mm_Celera | 1:160958215 | CAAATTAAAAAAATA[C/G]AATAAAGTGAAGATT | 381305 |
rs31751428 | snp | C/T | 0.5 | 0 | intron-variant | Rc3h1 | Mm_Celera | 1:160953610 | AAATGCTAATAGTTT[C/T]TCAGCTAGTGGTAGG | 381305 |
rs31761054 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160910893 | TGGATGAGTATTGGT[A/G]ACTGAACTCAGATTA | 381305 |
rs31774018 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Rc3h1 | GRCm38.p3 | 1:160972791 | AGATTTTAAGATTCT[A/G]TTTCTGTAATTGCTA | 381305 |
rs31781270 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160921082 | TTAAGCTAAGGAAAG[A/G]TGTGAATTTGAGGCT | 381305 |
rs31794266 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160949697 | ATGTGGTCTATGTAG[C/T]GTGTGTGGATGTTTT | 381305 |
rs31795622 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rc3h1 | GRCm38.p3 | 1:160922695 | TCTTTTTTTTCTCCC[C/T]TTTTTTTTTATTAAG | 381305 |
rs31797549 | snp | A/T | 0.32 | 0.24 | intron-variant | Rc3h1 | Mm_Celera | 1:160949329 | GTATCAAACACAGGA[A/T]ATTTATTTATTTGGG | 381305 |
rs31808063 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Rc3h1 | Mm_Celera | 1:160946032 | ATGAAAGCTAGTCAA[A/G]AGGGAGGAAGATTCC | 381305 |
rs31820253 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rc3h1 | Mm_Celera | 1:160916039 | TTGAGTTGAAATTTT[C/T]GTACAAGGTAAAAGA | 381305 |