SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6298685 | snp | A/C | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96758126 | AACCACCTAATGCTG[A/C]ATCACTGAGGATGGN | 67845 |
rs6298701 | snp | A/C | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96758141 | NATCACTGAGGATGG[A/C]TGTGTGAGAAGANTG | 67845 |
rs6298734 | snp | A/G | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96758154 | GGNTGTGTGAGAAGA[A/G]TGCAGTCAGGGNTAA | 67845 |
rs6298749 | snp | A/G | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96758166 | AGANTGCAGTCAGGG[A/G]TAACCTGGGAAGATC | 67845 |
rs6300366 | snp | C/G | 0.290657 | 0.246672 | intron-variant | Rnf115 | Mm_Celera | 3:96758450 | AACATGGTAGTTGCT[C/G]TGAAATAAGTATATT | 67845 |
rs6403753 | snp | G/T | 0.290657 | 0.246672 | intron-variant | Rnf115 | Mm_Celera | 3:96736292 | GAATTTAGAGATACC[G/T]GTTAGAAGCTGGAGT | 67845 |
rs6403796 | snp | G/T | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96736322 | TCAGCTGCTGAGGGG[G/T]TCTTTCCTCCACCTG | 67845 |
rs6405447 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf115 | Mm_Celera | 3:96736625 | CTTAATAACCATTAC[C/T]AGCTTCCTGCTCTCC | 67845 |
rs6407016 | snp | A/T | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96730311 | tttcagtttttATTT[A/T]CATTTGTTTGTTGTG | 67845 |
rs13469988 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Rnf115, Polr3c | Mm_Celera | 3:96727859 | CTCCGCTGTCGCCGC[A/G]CACCGTTTCTTCTGC | 67845 |
rs13469989 | snp | A/C | | | utr-variant-3-prime | Rnf115 | GRCm38.p3 | 3:96790471 | GTATCTGCTCCTGGC[A/C]CCATTAGCAAGGTAA | 67845 |
rs30430767 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf115 | GRCm38.p3 | 3:96780892 | GCACATAATAGTGAA[C/T]GCAGTCATGAAAAAG | 67845 |
rs30608641 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf115 | Mm_Celera | 3:96750512 | ACCTTTATCTTGTTC[C/T]TCTCTGTCTTGGTTA | 67845 |
rs30701252 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf115 | Mm_Celera | 3:96739286 | GTAGTGCAGTTAGTG[C/T]TGACCATATGGTCAT | 67845 |
rs30940871 | snp | C/T | 0.5 | 0 | intron-variant | Rnf115 | GRCm38.p3 | 3:96740629 | TTCCTTCCTTCCTTC[C/T]TTCCTTCTTTCCTTC | 67845 |
rs31497257 | snp | C/T | 0.255 | 0.24995 | intron-variant | Rnf115 | Mm_Celera | 3:96757588 | CTGGTTAAATGGTTT[C/T]GTGCTGAAATAGTTT | 67845 |
rs31547100 | snp | A/G | 0.5 | 0 | intron-variant | Rnf115 | GRCm38.p3 | 3:96749139 | GTTGTCACCAGAGAT[A/G]CTCCCTACTGATTTC | 67845 |
rs31547156 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf115 | GRCm38.p3 | 3:96771997 | TTAAAGTATGTAATT[C/T]ACCAGTGTAGCATGT | 67845 |
rs31640556 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf115 | GRCm38.p3 | 3:96750579 | CAATTCTTTTTTTTT[A/T]AAAAAAGGTTTTATT | 67845 |
rs31721044 | snp | A/G | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96756844 | AGACTTAACTAGGGT[A/G]TGTTTGTTTCCTCAG | 67845 |
rs36253726 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96765817 | ATTTACCTTTCAGTG[C/T]CATCTATAGCCATTA | 67845 |
rs36265394 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96744300 | GTTGTCTGCTCTCTT[A/G]GATAGGAAGGGCAAG | 67845 |
rs36304280 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96737024 | AGCCAGACTCAGTGT[A/G]CTCAGAAACCAGGTA | 67845 |
rs36312826 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96743951 | TAGTGCATTCAATTC[C/T]TATTCCTTCCCTTGC | 67845 |
rs36365881 | snp | A/C | 0.391111 | 0.206368 | intron-variant | Rnf115 | Mm_Celera | 3:96759294 | CCAGATGGGAAAACC[A/C]AGCTCATTGGACAGC | 67845 |
rs36445561 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96743638 | ATGGAACCGGATTCT[A/G]CAACAGAGCAGGGTC | 67845 |
rs36459841 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rnf115 | Mm_Celera | 3:96757108 | AAAGAGGTATTTTAT[C/T]AATTAGTCATGTGCT | 67845 |
rs36483560 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96737100 | CAGAAGCTGCTTGGA[C/G]CTGAGAGGTTTAAGG | 67845 |
rs36503104 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf115 | Mm_Celera | 3:96744161 | TCCTTGGATAGTCCG[A/C]ACTTGGTGCTACGTG | 67845 |
rs36584687 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96763942 | TTTTGTATCTGTATT[A/C]TTTTCAGATTCCTTC | 67845 |
rs36588448 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rnf115 | Mm_Celera | 3:96757246 | ATTATAAAATACAGT[G/T]TTTGGCCTTTCGGTT | 67845 |
rs36602331 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96734500 | GGCTTTAGACTCACT[A/G]TGTAACTCAGGATAT | 67845 |
rs36603647 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf115 | Mm_Celera | 3:96744159 | TCTCCTTGGATAGTC[C/T]GAACTTGGTGCTACG | 67845 |
rs36608838 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96736973 | TCTCTGCTGTTTCTT[C/T]AGCTATTAAATGGTT | 67845 |
rs36647112 | snp | C/T | 0.5 | 0 | intron-variant | Rnf115 | Mm_Celera | 3:96755363 | ATGCCAGCATTATGC[C/T]TGTAAGATTAGCATG | 67845 |
rs36654430 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf115 | Mm_Celera | 3:96777792 | GCCCAAACGTGGACC[A/G]TATAGTCAGTAGCAG | 67845 |
rs36678890 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96737172 | TTGCACTTCAGGCCC[A/G]GTGCCATGATTGTGT | 67845 |
rs36684078 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96762297 | GTTGCTTAGATAATG[C/T]GAAACTATTTTGTAT | 67845 |
rs36731079 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rnf115 | GRCm38.p3 | 3:96747040 | GGCTGATAGGCTGCA[C/T]TGGCTGGTTGCTTCC | 67845 |
rs36753588 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf115 | Mm_Celera | 3:96749770 | AAGAAGCAGATGATC[A/T]GCACTGTGCTCTCTC | 67845 |
rs36778808 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rnf115 | Mm_Celera | 3:96734103 | TGGGTTCAATCCCTA[C/G]TAACTTTAGCTGGAT | 67845 |
rs36781167 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf115 | Mm_Celera | 3:96755328 | GGATGTTGGTGTAAC[A/G]GTTTTGGCTTTAAAT | 67845 |
rs36796727 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Rnf115 | GRCm38.p3 | 3:96747046 | TAGGCTGCATTGGCT[A/G]GTTGCTTCCTGTTAC | 67845 |
rs36800871 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Rnf115 | Mm_Celera | 3:96756871 | TCAGTGAGCTCAGTG[C/G]AGTGTCTGGAGTAGT | 67845 |
rs36811129 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf115 | Mm_Celera | 3:96743039 | AAAACTGAAAATGCT[C/T]ACCTGGAACTTTGGC | 67845 |
rs36866883 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf115 | Mm_Celera | 3:96777856 | ACTATTTCTTGAACT[A/G]TGTATGACCAGAAAA | 67845 |
rs36875991 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96740213 | TGTCTTCATTCCCTA[G/T]CCTTCTTCATCTTTG | 67845 |
rs36897306 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf115 | Mm_Celera | 3:96777934 | ATCTACTTTTCACTA[A/G]TGGGACTCTAACAGT | 67845 |
rs36956860 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96765798 | GAACAGCTACTCTGA[C/T]GCTATTTACCTTTCA | 67845 |
rs36961660 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rnf115 | Mm_Celera | 3:96738397 | TGCTTTGATATGCAC[C/G]TACACAGTGAAATGA | 67845 |
rs36969257 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf115 | Mm_Celera | 3:96755927 | CTGGTGAAGTCAGTG[G/T]TTTTAAAGAGGAAAG | 67845 |
rs36973968 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rnf115 | Mm_Celera | 3:96774039 | ATAACATCATGTATG[C/T]CCTGTGAGCAACCGT | 67845 |
rs36977701 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf115 | Mm_Celera | 3:96752852 | TCTTGTTCATTAAAG[A/G]CTGAGAATATTATGT | 67845 |
rs36985194 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf115 | Mm_Celera | 3:96763500 | ACGTCTCTAAGATTA[C/T]GCATGCGCTCAAACA | 67845 |
rs36995881 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Rnf115 | Mm_Celera | 3:96752281 | CAGTTGAAAATGCCT[A/T]TCTTAAGTATGTTTA | 67845 |
rs37043007 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96744063 | AGTGAAATGTTTCAG[C/T]AAAGCCTTTGCTATG | 67845 |
rs37086990 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96776307 | TGATACTTCTCGCTC[A/G]TAAGCATTTGGCAGG | 67845 |
rs37088280 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf115 | Mm_Celera | 3:96737501 | TGTTTTGACCCAATC[A/G]TCAGTTGTAGTACTG | 67845 |
rs37093398 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96737062 | TATTTAAGCAGACTG[C/T]ACAGGAACCCAGGAT | 67845 |
rs37160343 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf115 | Mm_Celera | 3:96734627 | TTAGACAGTGTTTCT[A/G]TAGTCCAGGTTGATC | 67845 |
rs37191012 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96757741 | TTTGATGTAGCTTTA[A/C]TTTATTTGAAAACCA | 67845 |
rs37199957 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf115 | Mm_Celera | 3:96756943 | GGGCTCTGGTTAGGA[C/T]GCTTGCTTCTGTTTG | 67845 |
rs37229235 | snp | C/G | 0.32 | 0.24 | intron-variant | Rnf115 | Mm_Celera | 3:96759794 | CAGGGTGTGCTGTTT[C/G]TGGGAGCACAGTCTG | 67845 |
rs37243113 | snp | C/G | 0.297521 | 0.245442 | intron-variant | Rnf115 | Mm_Celera | 3:96742994 | GAGAAATAAAATGAA[C/G]ATTGTGAATGTTACT | 67845 |
rs37294029 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf115 | Mm_Celera | 3:96763766 | AGATGCATTATAGTT[C/T]ATAATATAAAATCAT | 67845 |
rs37315384 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf115 | Mm_Celera | 3:96736632 | ACCATTACCAGCTTC[C/G]TGCTCTCCTGTGGTC | 67845 |
rs37352674 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96743667 | TCTTTGACCTGCAGT[A/T]ATCACTTGGCTTGGA | 67845 |
rs37371049 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf115 | Mm_Celera | 3:96746984 | AGGAATGGTAAGAAC[A/G]TCATAGGAGAAATTA | 67845 |
rs37491135 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Rnf115 | Mm_Celera | 3:96777477 | CTCCACAAGCCTTTA[A/G]ATGAAACAACAAACT | 67845 |
rs37579667 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96735304 | TTGAGTGGGGCTGTT[G/T]AGCTCCTCAGGGAAC | 67845 |
rs37588605 | snp | A/C | 0.142012 | 0.225474 | intron-variant | Rnf115 | Mm_Celera | 3:96775180 | TGTACAACAGAGGCT[A/C]TCATCAGTCATAGCT | 67845 |
rs37701777 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96757898 | CGCTGTTCTCATTTG[A/G]CCCGACCTATATTTA | 67845 |
rs37705344 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Rnf115 | GRCm38.p3 | 3:96746965 | ATTGTACTCCATGCC[A/T]TAAAGGAATGGTAAG | 67845 |
rs37720507 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Rnf115 | Mm_Celera | 3:96777270 | TTTGTATCCTTTACT[A/G]TGAGGTGGCAAGGAG | 67845 |
rs37768715 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf115 | Mm_Celera | 3:96756600 | CCAACAACTGCACAA[C/T]CTAGGGAAGATAATC | 67845 |
rs37782447 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf115 | Mm_Celera | 3:96757491 | CTGAATTCTTTCTAA[C/T]CTGCTAATCTAGACT | 67845 |
rs37830335 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96763019 | CTTTTAAGTAATCAG[A/T]GCATCCCTGGGTAAC | 67845 |
rs37964628 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96737544 | TGCTTTGCTCAAGGC[A/G]ACTTAAAGAGAGTGT | 67845 |
rs38182332 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96737896 | ATATGTAAGTTGAGG[C/T]TAAAGGCCAAAAGAT | 67845 |
rs38239522 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96763471 | TTTGAAACTAGAGAT[A/G]TAAAGCTCAGGGTAC | 67845 |
rs38301895 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf115 | Mm_Celera | 3:96774353 | TAGGGCAATAACAAC[A/G]AAATGGCTTATGGAC | 67845 |
rs38923996 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96744125 | GTTTTGAGACTGTTT[A/G]AACCTTGAAGAAATG | 67845 |
rs38944844 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96734708 | GTCTTCTTATCTGTG[A/T]TAGGATTGTCCTTGC | 67845 |
rs38981026 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96738516 | AAAGTACCTAAAATG[A/G]GGATATTCAGAAAAG | 67845 |
rs38987906 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf115 | Mm_Celera | 3:96754857 | CCAGGAAACTGAGTT[C/G]TTGCTTTGCCTTGGA | 67845 |
rs38996958 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf115 | GRCm38.p3 | 3:96751870 | ACAAGTGCTATTTTT[C/T]TTTTATCACTACAGT | 67845 |
rs39068380 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf115 | Mm_Celera | 3:96737550 | GCTCAAGGCAACTTA[A/G]AGAGAGTGTAAGAAT | 67845 |
rs39099176 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf115 | Mm_Celera | 3:96753466 | CTTAGGTAGTTATGC[A/C]ACCATTCTGTAAATA | 67845 |
rs39114249 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96757627 | TAGACTCTTTGAAGA[C/T]ACATATTTACTTTTC | 67845 |
rs39384332 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf115 | Mm_Celera | 3:96756912 | TGAAGATGAAGGCAG[C/T]TTTCAGTCCTTAGAA | 67845 |
rs39465194 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96743985 | AGACCAGTGTTTGGC[A/G]TTCTCCCGTGTTCTT | 67845 |
rs40105436 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf115 | Mm_Celera | 3:96742651 | TCTCTCTCTGAAGTG[A/G]ATGCTTGGGATGTGA | 67845 |
rs45687922 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96786382 | GAAAACTTTTTTACC[A/G]CCTAAAATTGAAACT | 67845 |
rs45827212 | snp | C/T | | | intron-variant | Rnf115 | Mm_Celera | 3:96779876 | CCTGCATCTTTTAAG[C/T]CCTTGATGGTGGCAG | 67845 |
rs45868288 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96786768 | AGAGGTGTGATTTTC[C/G]GATTGTCATGGAGGC | 67845 |
rs46002598 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf115 | Mm_Celera | 3:96788272 | TACTATTTCTGTCTC[C/T]ATTTTGAATACAATT | 67845 |
rs46046870 | snp | A/C | | | intron-variant | Rnf115 | Mm_Celera | 3:96779896 | CTGTGGTGGGAACCA[A/C]CACCCCTGCATCTTT | 67845 |
rs46064934 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96786575 | TCATCCTTCTGATAG[A/G]GGGTCCTCAGATGGA | 67845 |
rs46134326 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf115 | Mm_Celera | 3:96784884 | TCTGGATTGTAGAGG[A/G]CTAGTGACTTGGAGC | 67845 |
rs46228194 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf115 | Mm_Celera | 3:96783392 | TGTCTAGTCAGCCAC[A/G]ATTATCTGTGGAATA | 67845 |