SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6360812 | snp | C/T | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57822856 | TTCTTCCCCAGAAGT[C/T]TGTATACTCTGATAC | 24017 |
rs6361413 | snp | A/T | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57822978 | CTTATTGTCCAACTC[A/T]GATGTGCAGCCAGCA | 24017 |
rs6362611 | snp | C/T | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57823250 | AGGTGGGCAAAATCT[C/T]TGTAGGCCAGCTGCT | 24017 |
rs6363066 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf13 | Mm_Celera | 3:57823293 | TATTTTAAAAAAGCA[C/T]TCACAAGGTCCAATG | 24017 |
rs6363542 | snp | A/C | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57744007 | GCCCCCCCCCCCCCA[A/C]GCcatataccaaaaa | 24017 |
rs6364095 | snp | C/T | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57744100 | aacacatttgtttag[C/T]tttgaaacattttta | 24017 |
rs6364606 | snp | C/T | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57744151 | taaaccattagcagt[C/T]ctgtctcctgatttc | 24017 |
rs6365205 | snp | A/G | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57744260 | aaatgttatatgatt[A/G]attatgcctggcttc | 24017 |
rs6365753 | snp | G/T | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57744368 | TTTATTTAGTCATTG[G/T]TGAATATTTGGATTG | 24017 |
rs6366234 | snp | A/G | 0.5 | 0 | intron-variant | Rnf13 | Mm_Celera | 3:57744427 | GTTTCTGTTAAATGA[A/G]GGTTTGTTTGAGTCC | 24017 |
rs6366310 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf13 | Mm_Celera | 3:57744468 | TTCTTTAGGTTTATC[C/T]CAAGAGTGAAATTGC | 24017 |
rs13477130 | snp | G/T | 0.42 | 0.183303 | synonymous-codon, downstream-variant-500B, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57833682 | GTCATTTGGGTCTCT[G/T]TCAGAATCCCACTCA | 24017 |
rs16782953 | snp | C/G | 0.104938 | 0.20361 | intron-variant | Rnf13 | Mm_Celera | 3:57779571 | NNAAGAAAGATATGT[C/G]AGTGCATTAAATTAT | 24017 |
rs16782954 | snp | A/C | 0.099723 | 0.199792 | intron-variant | Rnf13 | Mm_Celera | 3:57802568 | CAAAAANNCTATGTA[A/C]CTTCAGACTGTNCCT | 24017 |
rs16782955 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802580 | GTANCTTCAGACTGT[C/T]CCTTATTGTAGAATA | 24017 |
rs16807515 | in-del | -/A | 0.35503 | 0.226867 | intron-variant | Rnf13 | Mm_Celera | 3:57761889 | GTCATTTCTACTTTG[-/A]AATGCTNTCNCTGTT | 24017 |
rs16807516 | snp | A/G | 0.172336 | 0.23763 | intron-variant | Rnf13 | Mm_Celera | 3:57761896 | CTACTTTGNAATGCT[A/G]TCNCTGTTCAGCTTG | 24017 |
rs16807517 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57761899 | CTTTGNAATGCTNTC[C/T]CTGTTCAGCTTGGTT | 24017 |
rs16807518 | snp | A/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57761981 | AACTTGAGGTTCATG[A/T]GCTCATCAGTGGCAG | 24017 |
rs16807519 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57762115 | TTCTAGACCCTTGGC[C/T]CTGGACATTGCACAC | 24017 |
rs16807520 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57762167 | GGAATGTGCATGCCA[C/T]CTCAGAAAGCAACTT | 24017 |
rs16807521 | snp | A/G | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57762186 | AGAAAGCAACTTGTG[A/G]AGATCCAAGTTCCTT | 24017 |
rs16807522 | snp | A/G | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57762314 | TTACATTTTTATTGT[A/G]GCAAAATCAGTCTAA | 24017 |
rs16807523 | in-del | -/A | 0.172336 | 0.23763 | intron-variant | Rnf13 | Mm_Celera | 3:57762384 | ttataaaattatgca[-/A]ctaacatcaaaatgt | 24017 |
rs16807524 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763018 | CTATAACTTTATTTT[C/T]CCTACCTCTATCTAN | 24017 |
rs16807525 | snp | A/G | 0.172336 | 0.23763 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763003 | NCCTACCTCTATCTA[A/G]AAATAATCCCTTCTG | 24017 |
rs16807526 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | GRCm38.p3 | 3:57762958 | GGACCCAAGTGAAGT[C/T]AANGCAAACTCCNAG | 24017 |
rs16807527 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Rnf13 | GRCm38.p3 | 3:57762955 | CCCAAGTGAAGTNAA[A/G]GCAAACTCCNAGTCC | 24017 |
rs16807528 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Rnf13 | GRCm38.p3 | 3:57762945 | GTNAANGCAAACTCC[A/C]AGTCCTCTGTTATCT | 24017 |
rs16807529 | in-del | -/T | 0.142012 | 0.225474 | intron-variant | Rnf13 | Mm_Celera | 3:57762766 | TATAGTATACATTTT[-/T]ATGAATAAATGAGAA | 24017 |
rs16807530 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | GRCm38.p3 | 3:57762684 | CCAAGTTATAAAGAA[C/T]CNCCTTTAATGATAT | 24017 |
rs16807531 | snp | A/G | 0.090703 | 0.192677 | intron-variant | Rnf13 | GRCm38.p3 | 3:57762682 | AAGTTATAAAGAANC[A/G]CCTTTAATGATATTG | 24017 |
rs16807533 | in-del | -/A | 0.444444 | 0.157135 | intron-variant | Rnf13 | Mm_Celera | 3:57762551 | GTAAATAGTTTTTNG[-/A]ANCACCATTTTACAA | 24017 |
rs16807534 | in-del | -/A | 0.345679 | 0.230967 | intron-variant | Rnf13 | Mm_Celera | 3:57762549 | AAATAGTTTTTNGNA[-/A]CACCATTTTACAAAG | 24017 |
rs16807536 | snp | C/T | 0.095 | 0.19615 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763659 | AAANAGACAACTTTG[C/T]TTTAAAATTGATTTT | 24017 |
rs16807537 | snp | A/T | 0.095 | 0.19615 | intron-variant | Rnf13 | Mm_Celera | 3:57763598 | GTTCCATATAAAAGT[A/T]CACATATGTTTGTTA | 24017 |
rs16807538 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Rnf13 | Mm_Celera | 3:57763574 | TTTGTTAAATATAAA[A/T]TNTGTAAtttgaggg | 24017 |
rs16807539 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Rnf13 | Mm_Celera | 3:57763572 | TGTTAAATATAAANT[A/T]TGTAAtttgagggag | 24017 |
rs16807540 | snp | G/T | 0.095 | 0.19615 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763520 | agcctagattcccta[G/T]gtagaccaggcagcc | 24017 |
rs16807541 | snp | A/C | 0.18 | 0.24 | intron-variant | Rnf13 | Mm_Celera | 3:57763490 | caggctgcctttgaa[A/C]tcatgaagactancc | 24017 |
rs16807542 | snp | C/T | 0.095 | 0.19615 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763477 | aantcatgaagacta[C/T]ccatctctaaaggtg | 24017 |
rs16807543 | snp | A/G | 0.095 | 0.19615 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763361 | acaacttaatttgta[A/G]atcaggctggncttg | 24017 |
rs16807544 | snp | C/T | 0.095 | 0.19615 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763350 | tgtanatcaggctgg[C/T]cttgaatgcacagtg | 24017 |
rs16807545 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf13 | Mm_Celera | 3:57763322 | gtgatccttgtacct[C/T]tgcctcccaagtnct | 24017 |
rs16807546 | snp | A/G | 0.095 | 0.19615 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763309 | ctntgcctcccaagt[A/G]ctggggttaATGATG | 24017 |
rs16807547 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf13 | Mm_Celera | 3:57763274 | ACACTTTTGTATGTT[A/T]TACttaattaaagaa | 24017 |
rs16807548 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Rnf13 | Mm_Celera | 3:57763190 | AAAATTCGGGTTTTG[A/T]ACCATTTCNNNTTTT | 24017 |
rs16807551 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Rnf13 | Mm_Celera | 3:57763179 | TTTGNACCATTTCNN[A/T]TTTTTTTTTTTTTGG | 24017 |
rs16807552 | snp | A/C/T | 0.176871 | 0.251609 | intron-variant | Rnf13 | GRCm38.p3 | 3:57763839 | AACCGTTATCCCCTG[A/C/T]NCTGTCAGAGTGAAC | 24017 |
rs16807553 | snp | A/G | 0.193906 | 0.258436 | intron-variant | Rnf13 | Mm_Celera | 3:57763840 | ACCGTTATCCCCTGN[A/G]CTGTCAGAGTGAACA | 24017 |
rs16807554 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rnf13 | Mm_Celera | 3:57763887 | TGCCAGGCAGAGGCT[C/T]TNCCACTGAACTGCA | 24017 |
rs16807555 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf13 | Mm_Celera | 3:57763889 | CCAGGCAGAGGCTNT[A/T]CCACTGAACTGCATC | 24017 |
rs16807556 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf13 | Mm_Celera | 3:57763937 | TCAGTGTCCTAGACT[C/T]TGAAAGGTCCGGNGA | 24017 |
rs16807557 | snp | G/T | 0.18 | 0.24 | intron-variant | Rnf13 | Mm_Celera | 3:57763950 | CTNTGAAAGGTCCGG[G/T]GATTTGAAATACCTT | 24017 |
rs16807558 | snp | G/T | 0.117188 | 0.211804 | intron-variant | Rnf13 | Mm_Celera | 3:57764132 | atgcactacaatgcc[G/T]ggcTTCCAAATATGT | 24017 |
rs16807559 | snp | C/T | 0.172336 | 0.23763 | intron-variant | Rnf13 | Mm_Celera | 3:57764148 | ggcTTCCAAATATGT[C/T]TTAATTTTAATATTA | 24017 |
rs16807560 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Rnf13 | Mm_Celera | 3:57764164 | TTAATTTTAATATTA[C/G]CACACTGTAATTNTA | 24017 |
rs16807561 | snp | G/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57764177 | TANCACACTGTAATT[G/T]TAAAAGGTTATTTTT | 24017 |
rs16807562 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Rnf13 | Mm_Celera | 3:57764214 | TAGGAATCAATGTGA[A/G]AAATGANGTGTTCTT | 24017 |
rs16807563 | snp | C/T | 0.095 | 0.19615 | intron-variant | Rnf13 | Mm_Celera | 3:57764221 | CAATGTGANAAATGA[C/T]GTGTTCTTTACAATT | 24017 |
rs16807564 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Rnf13 | Mm_Celera | 3:57764254 | TCTTTCCTCGTCTCC[A/T]AGGNGATTCACAANA | 24017 |
rs16807565 | snp | A/G | 0.32 | 0.24 | utr-variant-5-prime, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57764268 | CNAGGNGATTCACAA[A/G]ATGCTGCTCTCCATN | 24017 |
rs16807566 | snp | C/T | 0.489796 | 0.070696 | synonymous-codon, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57764283 | NATGCTGCTCTCCAT[C/T]GGGATGCTCATGCTG | 24017 |
rs16807567 | snp | C/T | 0.095 | 0.19615 | intron-variant | Rnf13 | Mm_Celera | 3:57768671 | gccctctgatacata[C/T]tcatttggagccatg | 24017 |
rs16807568 | snp | C/T | 0.46281 | 0.131194 | intron-variant | Rnf13 | Mm_Celera | 3:57768854 | ACATGAAGTTAGAAT[C/T]AAATTTAAATGGTTT | 24017 |
rs16807569 | snp | C/T | 0.095 | 0.19615 | intron-variant | Rnf13 | Mm_Celera | 3:57768939 | GATAAGCTGCAGTAG[C/T]AAATATGAATTATAG | 24017 |
rs16807570 | snp | A/T | 0.095 | 0.19615 | intron-variant, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57802118 | GTGGAGACATCTTAC[A/T]CTGGTGGCTTGTTTC | 24017 |
rs16807571 | snp | C/T | 0.090703 | 0.192677 | intron-variant, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57802231 | GCCCTTTTCTTTGTT[C/T]TTNAATAGTTAAATT | 24017 |
rs16807572 | snp | G/T | 0.46281 | 0.131194 | intron-variant, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57802234 | CTTTTCTTTGTTCTT[G/T]AATAGTTAAATTGTT | 24017 |
rs16807573 | snp | A/C | 0.090703 | 0.192677 | intron-variant, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57802307 | TTAAAAACTGTCTCT[A/C]CCTTGTAAGACTGTT | 24017 |
rs16807574 | snp | C/T | 0.090703 | 0.192677 | synonymous-codon, nc-transcript-variant | Rnf13 | Mm_Celera | 3:57802455 | TACGCAGTTGATACA[C/T]TAAAGAAAATTGACA | 24017 |
rs16807575 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802559 | ATTGGATATCAAAAA[C/T]NCTATGTANCTTCAG | 24017 |
rs16807576 | snp | A/G | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802560 | TTGGATATCAAAAAN[A/G]CTATGTANCTTCAGA | 24017 |
rs16807577 | snp | A/G | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802646 | atttatttagagaca[A/G]ggtctcactatgttg | 24017 |
rs16807578 | in-del | -/A/T | 0.0918136 | 0.197645 | intron-variant | Rnf13 | Mm_Celera | 3:57802693 | AAGATTGTTTTATAA[-/A/T]NNNNNNTATGCTAAT | 24017 |
rs16807585 | snp | A/T | 0.197531 | 0.244432 | intron-variant | Rnf13 | Mm_Celera | 3:57802780 | TGTATTTTGTATTAA[A/T]GGCAAATTCGATTAT | 24017 |
rs16807586 | snp | G/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802815 | TAAAATTGTTTTCAT[G/T]CTCCAGAGTGTTGCT | 24017 |
rs16807587 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802863 | TGCTAAGAAGATAGA[C/T]GTTCNATTTTGCAGT | 24017 |
rs16807588 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802868 | AGAAGATAGANGTTC[C/T]ATTTTGCAGTTTCTT | 24017 |
rs16807589 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57802916 | AGATTTTACTGTTTG[C/T]AATCACTGGCAGACT | 24017 |
rs16807590 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Rnf13 | GRCm38.p3 | 3:57796124 | TTGCCTAGAAGCACA[C/T]CATGTGCATCTGTGN | 24017 |
rs16807591 | snp | A/G | 0.224766 | 0.248723 | intron-variant | Rnf13 | GRCm38.p3 | 3:57796109 | NCATGTGCATCTGTG[A/G]GAATAAAGCGTAGAT | 24017 |
rs16807592 | snp | C/T | 0.110727 | 0.207612 | intron-variant | Rnf13 | GRCm38.p3 | 3:57796088 | AAGCGTAGATGTTCT[C/T]GAAAGATGTAGATGN | 24017 |
rs16807593 | snp | C/T | 0.099723 | 0.199792 | intron-variant | Rnf13 | GRCm38.p3 | 3:57796073 | NGAAAGATGTAGATG[C/T]CTATAGGAGAACACC | 24017 |
rs16807594 | snp | C/T | 0.104938 | 0.20361 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795938 | AAAGAAATCTATTGC[C/T]AAAACAGAAACTTNC | 24017 |
rs16807595 | snp | G/T | 0.104938 | 0.20361 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795924 | CNAAAACAGAAACTT[G/T]CCATGATCAGGCTGA | 24017 |
rs16807596 | snp | A/G | 0.110727 | 0.207612 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795899 | GGCTGAGGAATCACA[A/G]GTCANCNGGCTTTCA | 24017 |
rs16807597 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795894 | AGGAATCACANGTCA[C/T]CNGGCTTTCAAATCC | 24017 |
rs16807598 | snp | A/G | 0.110727 | 0.207612 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795892 | GAATCACANGTCANC[A/G]GGCTTTCAAATCCTT | 24017 |
rs16807599 | snp | G/T | 0.110727 | 0.207612 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795864 | CTTCTTAATACTTAC[G/T]AGCGGTATANACTCN | 24017 |
rs16807600 | snp | A/G | 0.104938 | 0.20361 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795854 | CTTACNAGCGGTATA[A/G]ACTCNGGNGAATTGC | 24017 |
rs16807601 | snp | C/T | 0.104938 | 0.20361 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795849 | NAGCGGTATANACTC[C/T]GGNGAATTGCTTCCT | 24017 |
rs16807602 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Rnf13 | GRCm38.p3 | 3:57795846 | CGGTATANACTCNGG[C/T]GAATTGCTTCCTCTG | 24017 |
rs16807603 | snp | A/G | 0.095 | 0.19615 | intron-variant | Rnf13 | Mm_Celera | 3:57806661 | GCATTCCCTAAATTG[A/G]GTgttctcaactttn | 24017 |
rs16807604 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf13 | Mm_Celera | 3:57806676 | NGTgttctcaacttt[C/T]ctaatgctgccaccc | 24017 |
rs16807605 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57806695 | atgctgccacccttt[C/T]aactacagtttntca | 24017 |
rs16807606 | snp | A/C | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57806707 | tttnaactacagttt[A/C]tcatgtggtgactcc | 24017 |
rs16807607 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57806727 | gtggtgactcccaac[C/T]ataaagntattttca | 24017 |
rs16807608 | snp | C/T | 0.090703 | 0.192677 | intron-variant | Rnf13 | Mm_Celera | 3:57806734 | ctcccaacnataaag[C/T]tattttcattgctac | 24017 |
rs16807609 | snp | A/G | 0.172336 | 0.23763 | intron-variant | Rnf13 | Mm_Celera | 3:57806837 | ccttgtgaaaaggcc[A/G]gtcaacccctaaagg | 24017 |