SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3023189 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Rnf150 | Mm_Celera | 8:82915140 | CTCACCACAAATATG[A/C]ACACACATGTACACA | 330812 |
rs3653966 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83001266 | GCAATTGTTTGAAAA[C/T]ACTATTTTCTATTTA | 330812 |
rs3655768 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83001489 | AATTTCCAGCATCAA[C/T]GTGGTGACTTACAAT | 330812 |
rs3656323 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Rnf150 | Mm_Celera | 8:82906647 | ATTACACACATCTGT[C/T]AACCAATCACCTGCA | 330812 |
rs3656997 | snp | A/G | 0.362812 | 0.2231 | intron-variant | Rnf150 | Mm_Celera | 8:82906779 | TTTGAAATGGAAAAA[A/G]TCTTTGATGAACATA | 330812 |
rs3657878 | snp | A/C | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82918872 | AAAAACACCCCAGCT[A/C]CCACTGTTAAGAGTT | 330812 |
rs3657911 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82918887 | ACCACTGTTAAGAGT[C/T]CCACAAAAACATCAA | 330812 |
rs3658566 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82919009 | TGCTTAGCTGATTCT[A/G]TGCAGCATGTTCTCT | 330812 |
rs3659123 | snp | G/T | 0.5 | 0 | intron-variant | Rnf150 | GRCm38.p3 | 8:82919075 | CCCGCTCCTTCAGTG[G/T]TATTCCCCAAGTTCC | 330812 |
rs3659199 | snp | C/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82919114 | GAGCCCTATGGAGAT[C/G]AATAATTTGGGTTCT | 330812 |
rs3659671 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82919152 | AGTGTTTTACTGTGG[A/G]TCTCTGCATCTGCTC | 330812 |
rs3659689 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82919163 | GTGGATCTCTGCATC[C/T]GCTCCCATCTGCTGC | 330812 |
rs3677456 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf150 | Mm_Celera | 8:82962798 | CTGAGTAAAGGAACT[A/G]AGGAGAGCACAGAAC | 330812 |
rs3677475 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf150 | Mm_Celera | 8:82962807 | GGAACTAAGGAGAGC[A/C]CAGAACCACTGACCT | 330812 |
rs3677552 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | GRCm38.p3 | 8:82962839 | GATGTGTCTCCCAGA[A/G]AAGCTAAACTCAGAA | 330812 |
rs3677555 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf150 | Mm_Celera | 8:82962842 | GTGTCTCCCAGAGAA[A/G]CTAAACTCAGAATCC | 330812 |
rs3678693 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Rnf150 | Mm_Celera | 8:82962977 | CAGGAGGATTCTGAT[A/G]GGCCAATTCAAGGGC | 330812 |
rs3679332 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf150 | Mm_Celera | 8:83061510 | CAGTGATTGGTCCAG[C/T]CAAGAGAGGGAGCTC | 330812 |
rs3680522 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Rnf150 | Mm_Celera | 8:83061635 | TTTGGTGTCCGCGTA[C/G]CACATCTCTTTATCC | 330812 |
rs3688640 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82967449 | TAAAAACACTGTAGC[C/T]GGTGAAGGAATCCTA | 330812 |
rs3688674 | snp | A/C | 0.5 | 0 | intron-variant | Rnf150 | GRCm38.p3 | 8:82967470 | AGGAATCCTATGCAC[A/C]TAAGACAAGAAAAGA | 330812 |
rs3689154 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Rnf150 | Mm_Celera | 8:82967506 | AGGGTGGCAAATGTT[A/C]AGGAGTGAAGAGGTT | 330812 |
rs3694593 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Rnf150 | Mm_Celera | 8:82960399 | AGGAGCCACAGAGCA[A/G]CCTGGTCTCACCCTT | 330812 |
rs3694681 | snp | G/T | 0.486111 | 0.0821678 | intron-variant | Rnf150 | Mm_Celera | 8:82960442 | GGCAGAATTATCAGA[G/T]ATCACGCCTGTCCCT | 330812 |
rs3694697 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | GRCm38.p3 | 8:82960447 | AATTATCAGATATCA[C/T]GCCTGTCCCTGTGCA | 330812 |
rs3698723 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82954507 | ACATTTTGAATTAAT[C/T]TTGTGTGTGTGTCTG | 330812 |
rs3698731 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82954516 | ATTAATCTTGTGTGT[G/T]TGTCTGTGTTTGTGT | 330812 |
rs3698769 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82954540 | TTTGTGTATTTCTGT[A/G]TGTGTATGCACACAT | 330812 |
rs3698790 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82954545 | GTATTTCTGTGTGTG[C/T]ATGCACACATGCACC | 330812 |
rs3700897 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Rnf150 | Mm_Celera | 8:82891974 | AGAGCTGTTCTTGTC[C/T]GAACACTCCCACTTA | 330812 |
rs3702640 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf150 | Mm_Celera | 8:82892271 | ATTTCCTTCTTGCTA[A/G]TAGTGATGGTGAGTG | 330812 |
rs3703347 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Rnf150 | Mm_Celera | 8:82892430 | CCTGGCATGAATCTT[G/T]GCACAGCAGCCTCAG | 330812 |
rs3703773 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82892437 | TGAATCTTTGCACAG[C/T]AGCCTCAGAAGATGA | 330812 |
rs3713940 | snp | C/T | 0.30839 | 0.243086 | intron-variant | Rnf150 | Mm_Celera | 8:82906382 | CTTAGTGTACCACAT[C/T]ATCACTCTAAATTTT | 330812 |
rs3714612 | snp | A/G | 0.362812 | 0.2231 | intron-variant | Rnf150 | Mm_Celera | 8:82906525 | GTTCACTGAGCTGGC[A/G]AGAGTAGGAAGCCAG | 330812 |
rs3727130 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83001147 | TTTCCTGCCAACCTG[A/G]GATCCCTAGGGAGAC | 330812 |
rs4138485 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82967394 | ATGCACATGAGCACG[C/T]ATGGTCACACACATA | 330812 |
rs4140312 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:82892460 | GAAGATGAATCCCAA[C/G]TTAGATACTGCTGAG | 330812 |
rs6214189 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Rnf150 | Mm_Celera | 8:82893396 | CAAAGTGTAGCTTCT[A/G]GCCTCTCATTTTCCC | 330812 |
rs6243228 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83006239 | AGACCGTGCTGCTGA[A/G]AGGCTGGCCCCAGGC | 330812 |
rs6244441 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83006485 | TTGCAAACAAGCAAA[A/G]CACTTCTTTCCCTGC | 330812 |
rs6257350 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83006573 | CTTGCATGAAAGGCA[A/G]ACCTAACAAGACAGC | 330812 |
rs6257750 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83006608 | ATCCATGCTGTGTGT[A/G]TAGTGGCAGCTCCTT | 330812 |
rs6260070 | snp | C/T | 0.235537 | 0.249581 | intron-variant | Rnf150 | Mm_Celera | 8:83046805 | AGTTCAGATGTCCCT[C/T]GCTACACTCTACCTG | 330812 |
rs6262150 | snp | A/G/T | 0.5 | 0 | intron-variant | Rnf150 | GRCm38.p3 | 8:83047207 | CTGCTGCAGCCCGCC[A/G/T]CAGCCANTCCAGGGG | 330812 |
rs6262165 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83047214 | AGCCCGCCNCAGCCA[A/G]TCCAGGGGGAGAAGG | 330812 |
rs6276923 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82947864 | GAAGCTGGACTCAAC[C/T]ATCTGCTCTCTTCTC | 330812 |
rs6298080 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Rnf150 | Mm_Celera | 8:82910535 | TGTGTGCCAAGTAAA[A/G]ATAAGACAGACAGTG | 330812 |
rs6302802 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82864920 | GTGTATCAAGAGGCA[A/G]GTCAACTTACCTGTC | 330812 |
rs6303515 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Rnf150 | Mm_Celera | 8:82937321 | TCTGTGTTTCTTGAG[G/T]TCTTCCATGAAATGG | 330812 |
rs6303992 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf150 | GRCm38.p3 | 8:82937391 | AAGGGTTTTTCTCAG[C/T]GAGGGCCAAGCAGTG | 330812 |
rs6311014 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Rnf150 | Mm_Celera | 8:82910611 | TGTCGCTTACTATAT[A/G]GTGTCCTTAACAACC | 330812 |
rs6311460 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Rnf150 | Mm_Celera | 8:82910664 | TTGAATAACCCAGCA[A/G]AGCACGTCACTACAG | 330812 |
rs6311503 | snp | A/T | 0.429688 | 0.173817 | intron-variant | Rnf150 | Mm_Celera | 8:82910689 | CTACAGCGTAAGTTC[A/T]CGATTACANCATTTT | 330812 |
rs6311522 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82910698 | AAGTTCNCGATTACA[C/T]CATTTTCAGAAATTT | 330812 |
rs6311558 | snp | A/C | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82910724 | AATTTGGTGTCTAAC[A/C]GAAATTACTGTCCTC | 330812 |
rs6385141 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83026824 | TTGCTTCCAATATTT[C/T]GTCATTCTGAAATCA | 330812 |
rs6385261 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83026900 | GCTGATTTATTGGGT[C/T]NAGTGTGATGTAGAA | 330812 |
rs6385262 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83026901 | CTGATTTATTGGGTN[C/T]AGTGTGATGTAGAAG | 330812 |
rs6386735 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83027122 | TTACCTTTCGCTAAC[A/G]TAATTTTATAGCTTA | 330812 |
rs6386846 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83027191 | GATGTTAGGCTAGAA[C/T]GGGACCTGTGACCTA | 330812 |
rs6387223 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83027218 | CCTAAAATTGATAAA[C/T]ATCTTCACTAGTTCT | 330812 |
rs6388264 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82954587 | AAATGCATACCCCTA[C/T]GGAAGTCAGAGAATG | 330812 |
rs6400372 | snp | G/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:83027328 | AGTTTTTAAAATTAT[G/T]TTGTAAAATGTGTGT | 330812 |
rs13479863 | snp | G/T | 0.46281 | 0.131194 | intron-variant | Rnf150 | Mm_Celera | 8:82939762 | TAACCAAACAATGAT[G/T]TTCCCTTCATGCAAC | 330812 |
rs30573961 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf150 | GRCm38.p3 | 8:82866422 | GAGCATATGAGTTTC[A/C]CTGTCAATCAATGTC | 330812 |
rs30577264 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Rnf150 | Mm_Celera | 8:82877578 | CCCTTATACACTGGT[A/C]ACTAGTATAGATTTT | 330812 |
rs30720720 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82869057 | TGGCAAGGATCTCTC[A/G]CTGGCCATGGAGTTT | 330812 |
rs30729519 | snp | A/G | 0.5 | 0 | utr-variant-5-prime | Rnf150 | Mm_Celera | 8:82863736 | CTCCCCCGCAAGTGC[A/G]CGGCGCCCGCTCCGC | 330812 |
rs30814128 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Rnf150 | Mm_Celera | 8:82877840 | TTTCAGCCTCTTGAA[C/T]TTTGTGACTTTCTTG | 330812 |
rs30816866 | snp | C/T | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82877763 | ACTCCACCCATTGAA[C/T]TTGGGAAGGGATGCC | 330812 |
rs30899927 | snp | A/C | 0.489796 | 0.070696 | intron-variant | Rnf150 | GRCm38.p3 | 8:82866555 | GGAATATGGTTATTT[A/C]GTGAGCTCAGATTGC | 330812 |
rs30930866 | snp | C/T | 0.5 | 0 | utr-variant-5-prime | Rnf150 | Mm_Celera | 8:82863616 | CACCCCCGCCCCGCT[C/T]GGCCGCGACAAGCAG | 330812 |
rs31008633 | snp | A/G | 0.5 | 0 | intron-variant | Rnf150 | Mm_Celera | 8:82877772 | ATTGAATTTGGGAAG[A/G]GATGCCTGATCCTAA | 330812 |
rs32534771 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82937693 | ATGTGTTGGTTCCTA[A/G]CACCTACACTGGGCA | 330812 |
rs32540374 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf150 | Mm_Celera | 8:83002198 | ACAAAAATAAACACA[A/G]GTATGCTTTTATAGG | 330812 |
rs32541146 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:82894334 | TAGGTGTGCAAGAGT[A/G]TGTGTGAGGTGGGTG | 330812 |
rs32542590 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf150 | GRCm38.p3 | 8:83008855 | TTACAATCTTCCCAC[C/T]CCCTCTTCCATGATG | 330812 |
rs32543907 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:82981781 | GCTTAGCTAATAAAC[C/T]GGAAACATTCCTGTT | 330812 |
rs32547941 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83045538 | CAGGGACCTTCTGTT[C/T]ACAATGAGAGGGGGA | 330812 |
rs32563634 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Rnf150 | Mm_Celera | 8:82929477 | AGGTTTAAGTGGACA[G/T]GGGACAAATACTACC | 330812 |
rs32573113 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rnf150 | GRCm38.p3 | 8:82928165 | GTGCTGCTCAGTCAT[C/T]GTCACTGACAGGTCT | 330812 |
rs32573974 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82910214 | TCAATAAACCTAACC[C/T]ATGTCATCTCTCACA | 330812 |
rs32580422 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83038624 | GTCTGATGCCTAACA[A/C]GTCTGTTAGATTTAA | 330812 |
rs32581698 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Rnf150 | Mm_Celera | 8:82977133 | GGGAGCAACATGTCC[A/G]TAGAAAGTATAAAGT | 330812 |
rs32582276 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Rnf150 | GRCm38.p3 | 8:82887941 | TTAGTTGGAGACCAT[A/C]CTGGGCTACACAGTG | 330812 |
rs32589527 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83037372 | GCAAGTGTGTATGCT[C/T]GCATGGATGCATGGA | 330812 |
rs32594936 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:83056861 | AGCACCAACATGATG[A/G]TTACAACCATCTGAA | 330812 |
rs32597008 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf150 | Mm_Celera | 8:82992418 | AGTAAAGACCCTTGA[C/T]ACTGACCCTGTTTCA | 330812 |
rs32602169 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:82929612 | TGTTCGTTTGTGTGT[G/T]TAACTCTGTGTAACT | 330812 |
rs32607453 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83012287 | AAGTCATAAGATTTC[C/T]TGAATTCATGTGGGA | 330812 |
rs32608921 | snp | A/T | 0.389273 | 0.207612 | intron-variant | Rnf150 | Mm_Celera | 8:82937549 | AGGGAGACAGGGAGA[A/T]GCTGAGAACAAGTGA | 330812 |
rs32609805 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83008062 | TCATCTAAAGCTTTA[A/G]CATAACTAAACGGTG | 330812 |
rs32611036 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf150 | Mm_Celera | 8:82982036 | AACACCCAAATGTGT[A/G]AAAATGTACAGGCTA | 330812 |
rs32612944 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf150 | Mm_Celera | 8:82979800 | TTTTATGTTTCAAAG[A/G]CAATTTGTTGAATAC | 330812 |
rs32614834 | snp | C/G | 0.415225 | 0.187619 | intron-variant | Rnf150 | Mm_Celera | 8:83043902 | AACTATTGGAAGATT[C/G]AAAGATGAAGGAATT | 330812 |
rs32615931 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf150 | Mm_Celera | 8:83008688 | CTGAGCCCCACCCCC[A/C]ACTATGTGGAGGGAT | 330812 |
rs32617311 | snp | A/T | 0.455 | 0.143091 | intron-variant | Rnf150 | GRCm38.p3 | 8:83007970 | TGTCACTCCATTGTA[A/T]TGAACAAGATCTGTT | 330812 |
rs32618756 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf150 | Mm_Celera | 8:83043173 | GGCAGAGAAACAACT[A/T]TCTGGCTGAAATATG | 330812 |
rs32620273 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Rnf150 | GRCm38.p3 | 8:82887736 | GGTACAATCATTGCT[A/T]ATTCTGCCAATTAAC | 330812 |