SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6244207 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Rnf103 | GRCm38.p3 | 6:71504946 | AGACCTAACTGTGTA[C/T]GAGGGCTGTTAGCAC | 22644 |
rs6376684 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf103 | Mm_Celera | 6:71497404 | GGAAAGATTGGGGAG[A/T]GGGGGAGGGTTGTCT | 22644 |
rs6376833 | snp | A/G | 0.5 | 0 | intron-variant | Rnf103 | Mm_Celera | 6:71497488 | GTTTTTTAAACTTTC[A/G]TTTTGAGTTTATTAA | 22644 |
rs6377791 | snp | C/G | 0.5 | 0 | intron-variant | Rnf103 | Mm_Celera | 6:71497608 | CAGGTGTGCTAACTG[C/G]CATAAAAACAANTCA | 22644 |
rs6377803 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf103 | Mm_Celera | 6:71497620 | CTGGCATAAAAACAA[C/G]TCAGCAAAGTAGTCA | 22644 |
rs6377833 | snp | G/T | 0.5 | 0 | intron-variant | Rnf103 | Mm_Celera | 6:71497638 | AGCAAAGTAGTCAGC[G/T]TAGTAGCTGTACTGA | 22644 |
rs6377882 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf103 | GRCm38.p3 | 6:71497668 | AGAGACCCATGGCAC[A/G]TGTATTTTTTTGCTT | 22644 |
rs6378886 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf103 | GRCm38.p3 | 6:71497817 | GGTAAGTAGATACAC[A/G]TAACATTAATGTAAC | 22644 |
rs6408108 | snp | A/G | 0.5 | 0 | intron-variant | Rnf103 | Mm_Celera | 6:71505186 | TATAAGCTTTATTTG[A/G]ATTTTCAAATTTTTA | 22644 |
rs6408585 | snp | C/T | 0.5 | 0 | intron-variant | Rnf103 | Mm_Celera | 6:71505233 | GACTTCAGGGCCTTT[C/T]TCTGTCTGTGTAATG | 22644 |
rs30071364 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Rnf103 | GRCm38.p3 | 6:71498640 | TGCATTTAAAGAGGA[C/T]GGAATGATGCTGTCA | 22644 |
rs30074507 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf103 | GRCm38.p3 | 6:71506551 | GTGTAAACACTGATT[A/T]AAAAAAAAAAATCAA | 22644 |
rs30115222 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf103 | GRCm38.p3 | 6:71495781 | ATCTAGACAAATAGT[G/T]TGATAGGCAAGATGA | 22644 |
rs30172261 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf103 | GRCm38.p3 | 6:71497671 | GACCCATGGCACATG[A/T]ATTTTTTTGCTTATG | 22644 |
rs30617089 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf103 | Mm_Celera | 6:71496408 | GATAGGTAACATTCT[C/T]TCTCTCCCAGTCACA | 22644 |
rs30646610 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf103 | GRCm38.p3 | 6:71504379 | CATACACAAGCCTGG[A/G]GCTTTACTTCCTGAA | 22644 |
rs30667114 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Rnf103 | Mm_Celera | 6:71509571 | TTTAAGATTGCTGCG[A/G]TATTCTAATACAACC | 22644 |
rs30667116 | snp | A/T | 0.35503 | 0.226867 | synonymous-codon | Rnf103 | GRCm38.p3 | 6:71509604 | ACTGGCTTCGTGGGT[A/T]AGGGCAGACTGGATG | 22644 |
rs30667118 | snp | A/T | 0.375 | 0.216506 | missense | Rnf103 | Mm_Celera | 6:71509626 | GACTGGATGTTTTAC[A/T]CTTCACACCCAGCCC | 22644 |
rs30667120 | snp | G/T | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf103 | Mm_Celera | 6:71510450 | TTAACCATGTGCAAT[G/T]TGTCCTTAATAAGCT | 22644 |
rs30667122 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Rnf103 | Mm_Celera | 6:71510465 | GTGTCCTTAATAAGC[C/T]TTGAGTATCTTACAG | 22644 |
rs30667161 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf103 | Mm_Celera | 6:71498802 | GAGAGGGTTTAGCCT[A/G]TACAAATTCTAGTTT | 22644 |
rs30667163 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Rnf103 | Mm_Celera | 6:71498917 | GGTGTGATGTCAGTC[A/G]TCTCTTTAAAGTTTT | 22644 |
rs30668084 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Rnf103 | Mm_Celera | 6:71510937 | TGGTTTTTGTAGGTG[C/T]TTTGCTGGATTACTG | 22644 |
rs30668086 | snp | C/T | 0.391111 | 0.206368 | downstream-variant-500B | Rnf103 | Mm_Celera | 6:71511103 | TTTGAAAAATCAGTA[C/T]TTAGCATATTCATCT | 22644 |
rs30668088 | snp | C/T | 0.391111 | 0.206368 | downstream-variant-500B | Rnf103 | Mm_Celera | 6:71511148 | ATAACTTTTTAGTCA[C/T]ACAAGGATTACCTTG | 22644 |
rs30668090 | snp | C/G | 0.48 | 0.0979796 | downstream-variant-500B | Rnf103 | Mm_Celera | 6:71511311 | ATTACAATTTTAATA[C/G]TTCTTCTTTTTCCCT | 22644 |
rs30668092 | snp | C/T | 0.391111 | 0.206368 | downstream-variant-500B | Rnf103 | Mm_Celera | 6:71511366 | AATCATGATGCTTTG[C/T]CCGTAAACAGTCACC | 22644 |
rs30668185 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rnf103 | Mm_Celera | 6:71499135 | AAGGCAATAGGCAGG[A/G]CTAAAATGCAGAAGA | 22644 |
rs30668187 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf103 | GRCm38.p3 | 6:71500348 | CAGTTTAACTGCTGG[A/G]CCTCTTCTCCTGTTT | 22644 |
rs30668189 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf103 | Mm_Celera | 6:71500508 | TTGAAAGAAGCTGAC[A/T]AGTTTGTTTGCTCTT | 22644 |
rs30668191 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71501134 | CACCAACCATTGCAA[A/G]AACTAATTTTTCTTT | 22644 |
rs30668193 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Rnf103 | Mm_Celera | 6:71501170 | GGTAGCAAAATCTGT[A/G]TGACATCTTTGTGAC | 22644 |
rs30669015 | snp | A/C | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71501313 | GCCGTTTATTTCCCA[A/C]TTTTGTAGATCGTTG | 22644 |
rs30669017 | snp | G/T | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71501544 | TAACTGTTTGTTCCC[G/T]ACTAGCTGTCCCATT | 22644 |
rs30669019 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf103 | Mm_Celera | 6:71502022 | TTTTATACTTGTGAA[A/G]CTAGATCCCTGTTAA | 22644 |
rs30669021 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf103 | GRCm38.p3 | 6:71502046 | CTGTTAAAATACTGA[A/G]CAATGTAGAAAATGT | 22644 |
rs30669023 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf103 | Mm_Celera | 6:71502346 | AGAAATTGCTTTAGA[A/G]ACTCTTTATAAAAAG | 22644 |
rs30669865 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf103 | Mm_Celera | 6:71502545 | GGGGATTGTATAGAA[C/T]AAGCTGTAAAAAGCT | 22644 |
rs30669867 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71502651 | TTGCCCTATATTTAG[C/T]CTGTATGCCAGGTCT | 22644 |
rs30669869 | snp | A/G | 0.5 | 0 | intron-variant | Rnf103 | Mm_Celera | 6:71502672 | TGCCAGGTCTTTTTC[A/G]GGCTTGAAATTCACC | 22644 |
rs30669871 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf103 | Mm_Celera | 6:71502791 | GCACTGTAGGTGCCA[C/T]TTCAGATCATGCCTA | 22644 |
rs30669873 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71502889 | AGATTTTGTTTTGCC[A/G]TTAACTGAGCCAATG | 22644 |
rs30670645 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Rnf103 | GRCm38.p3 | 6:71502996 | TTCAGTTGACTAACT[A/G]CATAGGATTTTAACA | 22644 |
rs30670647 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71503112 | CTCTCTCAGTGGGGG[A/G]TCCTTCAACTCTTCC | 22644 |
rs30670649 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf103 | Mm_Celera | 6:71503585 | TTACACAGAGGCTCA[C/T]CTGAGAAGTCCAGGT | 22644 |
rs30670651 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71503736 | TTAGTGTTCTATGTT[C/T]CACTTCCTGAGCCAC | 22644 |
rs30670653 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71504426 | AAATGGTTCTTCCTG[C/T]CAGAAAGATTAGAGG | 22644 |
rs30671455 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Rnf103 | Mm_Celera | 6:71504510 | ATTTATGAAAGCTTA[G/T]GTCTATATATGCTGG | 22644 |
rs30671458 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Rnf103 | GRCm38.p3 | 6:71505051 | GGAAAAAGTCCTACG[A/C]GTAGCACCGATTTAA | 22644 |
rs30671460 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf103 | Mm_Celera | 6:71505377 | TCTTTTCTAGCTGGA[C/T]AGATGTAACTTCTGT | 22644 |
rs30671462 | snp | C/G | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71505873 | ATTAAGAAATTCCGA[C/G]TTTGAACCCTGACCA | 22644 |
rs30672314 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71505968 | ATGTTTGTAGCTTGT[A/G]TAAACTGGTGTTTGT | 22644 |
rs30672316 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Rnf103 | Mm_Celera | 6:71506026 | GTCTGTAGTCCTTTG[C/T]TTCAGTATTCTCCAA | 22644 |
rs30672318 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71506127 | TGGATTACAGGCATA[C/T]ACAACCACTTCCGTA | 22644 |
rs30672320 | snp | C/T | 0.165289 | 0.235211 | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71506347 | GTTTGTCATTGACTT[C/T]GGTATTCAGTCTATC | 22644 |
rs30672322 | snp | G/T | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71506689 | TATAATGAAACGCTA[G/T]CACAAAACAAAGCTC | 22644 |
rs30673084 | snp | C/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71506923 | CATTAGAGATTTTTT[C/T]CCCAAACATGGAAAA | 22644 |
rs30673086 | snp | C/T | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Rnf103 | GRCm38.p3 | 6:71507100 | CAAAGCAAGATTTCG[C/T]GTCATAAAGATGTCA | 22644 |
rs30673088 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71507578 | ACATAAGAAATCAAG[A/T]GGTGGGCTGGAGAGA | 22644 |
rs30673090 | snp | A/C | 0.426035 | 0.177515 | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71507940 | TAAGTAACGTGATGG[A/C]TGTTTTAGTTTTTGG | 22644 |
rs30673092 | snp | C/G | 0.492188 | 0.0620098 | intron-variant, missense, upstream-variant-2KB | Rnf103 | GRCm38.p3 | 6:71507994 | AGAGGTGACAAATGT[C/G]ATATCAAGAACTTGC | 22644 |
rs30673904 | snp | A/G | 0.375 | 0.216506 | intron-variant, missense, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71508025 | TGGGGACCAAAAGGA[A/G]TAGAGTCACTGACCT | 22644 |
rs30673906 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf103 | Mm_Celera | 6:71508062 | TAAATGTACACAGGT[A/G]GTGATTATAATTATG | 22644 |
rs30673908 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Rnf103 | Mm_Celera | 6:71508177 | GTTGTTTTTATGGTA[C/T]TCATTAAAGAGAAAA | 22644 |
rs30673910 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf103 | Mm_Celera | 6:71508349 | AAGGACTCTGAACCA[C/T]CTCAGGGACTCAGCA | 22644 |
rs30673912 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Rnf103 | Mm_Celera | 6:71508616 | GTGGCACATAAGAGA[G/T]GCTAAAGTATTTTCT | 22644 |
rs30674894 | snp | A/C | 0.375 | 0.216506 | utr-variant-5-prime, intron-variant | Rnf103 | Mm_Celera | 6:71508697 | ACAGAAATTTAAAGA[A/C]GACTACAGTGAACTT | 22644 |
rs30674896 | snp | A/G | 0.426035 | 0.177515 | utr-variant-5-prime, intron-variant | Rnf103 | Mm_Celera | 6:71508761 | CTCTTTGGTTACTTG[A/G]AGATTATCTGGTCTG | 22644 |
rs30674898 | snp | A/C | 0.375 | 0.216506 | missense | Rnf103 | Mm_Celera | 6:71509550 | AGATAGCTTTTATGA[A/C]TATAGTTTAAGATTG | 22644 |
rs30758240 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf103 | GRCm38.p3 | 6:71497483 | CTCTAGTTTTTTAAA[C/G]TTTCGTTTTGAGTTT | 22644 |
rs30793769 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rnf103 | GRCm38.p3 | 6:71492273 | ATAACAGTGCTATAC[C/T]GTGAAATCAAGAATG | 22644 |
rs30851640 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf103 | GRCm38.p3 | 6:71501368 | GGCATCAAAAATCAA[A/G]CATTATTTTGTTTTA | 22644 |
rs30868241 | snp | A/C | 0.5 | 0 | intron-variant | Rnf103 | GRCm38.p3 | 6:71498402 | CTTCCCATTTATTTC[A/C]TCAGTGCTTTTGATC | 22644 |
rs30902618 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf103 | GRCm38.p3 | 6:71498713 | TTTCATTGGATACCC[C/T]TGGCCTTCCCTTTTT | 22644 |
rs47446556 | snp | C/T | | | missense | Rnf103 | GRCm38.p3 | 6:71510161 | AAAGGAAGAGGAGGT[C/T]GTATGGATCACATAA | 22644 |
rs52195328 | snp | A/G | | | upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71492093 | TAACTTTTAAACTCT[A/G]GCCTGTCTGGCTCCA | 22644 |
rs211713019 | snp | C/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71496711 | TATTCAAAAGCTATT[C/G]AATTTTGTAGAATAA | 22644 |
rs211713777 | snp | A/G/T | | | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71506394 | TCGTATTTCATTTTT[A/G/T]ATTAAATTTAGATTT | 22644 |
rs211723913 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71507758 | AATAAATAAATCTTT[-/A]AAAAAAAAAAAAAGA | 22644 |
rs211780549 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71505357 | TAGCATACTGCACTT[A/G]TGTTTCTTTTCTAGC | 22644 |
rs211837665 | in-del | -/T | | | upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71493168 | CAGCTGTGCCACCCC[-/T]CCCCCCCACCCCACC | 22644 |
rs212212980 | in-del | -/A | | | intron-variant | Rnf103 | Mm_Celera | 6:71498187 | AGACTGAATGTGGCC[-/A]AAATTAAGAATGTAG | 22644 |
rs212478224 | snp | A/C | | | intron-variant | Rnf103 | Mm_Celera | 6:71497613 | GTGCTAACTGGCATA[A/C]AAACAAGTCAGCAAA | 22644 |
rs212669949 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71498406 | CCATTTATTTCCTCA[A/G]TGCTTTTGATCTCCC | 22644 |
rs213020401 | snp | C/T | | | intron-variant | Rnf103 | Mm_Celera | 6:71499295 | TTTTTACTATGTATA[C/T]GGGTGTTTTGCCCTA | 22644 |
rs213320842 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71502180 | AAAAAACAGGCAAAA[A/G]TATATTTGCAAACAC | 22644 |
rs213443110 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71498292 | TCCTGGGACTGCTCC[A/G]CAGTATTGCACTAGG | 22644 |
rs213476124 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71497925 | ACATGGTGGCTCACA[A/G]CCATCTGTAATGAGA | 22644 |
rs213694140 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71500075 | GCAAAAACAGTGCCT[A/G]TTAAGATAGTTGAGA | 22644 |
rs213977670 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71508529 | ACTGGTTTCACATCC[A/G]TAACAGGAGTTTTAA | 22644 |
rs214409895 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71501056 | CTAAAAATTACATCT[A/G]CTTTCTTGTGGTAAG | 22644 |
rs214570287 | snp | C/T | | | utr-variant-5-prime | Rnf103 | Mm_Celera | 6:71494644 | CGTCCCGGCTCCTGG[C/T]GACGCCAAGAGGGCG | 22644 |
rs214608482 | snp | A/C | | | upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71493730 | GTGACTAAACATCAG[A/C]GCATCAGAGGGCTGG | 22644 |
rs214993008 | snp | A/T | | | intron-variant | Rnf103 | Mm_Celera | 6:71504052 | TCATGTATTTTCATT[A/T]AATGCAGTATCAAAA | 22644 |
rs215063363 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71499432 | GAGTATCAAAATTAG[A/G]TCCTCTGGAAGAGCA | 22644 |
rs215196085 | snp | C/T | | | downstream-variant-500B | Rnf103 | Mm_Celera | 6:71511150 | AACTTTTTAGTCACA[C/T]AAGGATTACCTTGTA | 22644 |
rs215224867 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Rnf103 | Mm_Celera | 6:71506552 | TGTAAACACTGATTT[-/A]AAAAAAAAAATCAAC | 22644 |
rs215264198 | snp | A/G | | | intron-variant | Rnf103 | Mm_Celera | 6:71502937 | CTAGCATTTTATAGT[A/G]ACCATTTAATTCAAC | 22644 |
rs215394034 | snp | G/T | | | intron-variant | Rnf103 | Mm_Celera | 6:71502258 | GTAGTTGCATAGCAA[G/T]ATGCCATTTATACTA | 22644 |