SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13471568 | snp | A/T | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80198721 | TTCTCAGGCCCTCTC[A/T]TCTGGACAGAAGTAC | 71956 |
rs28227521 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Rnf135 | GRCm38.p3 | 11:80192620 | AAATCATCACCCTCT[A/G]GGAGAGAAGCCTTCA | 71956 |
rs28227522 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf135 | Mm_Celera | 11:80192428 | CATGTGTGATCTGAA[C/T]TGTGGCAGTGTCTGT | 71956 |
rs28227523 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Rnf135 | GRCm38.p3 | 11:80192341 | CATAGATAGCATTTT[A/G]ATGAACTTCTTTCTC | 71956 |
rs28227524 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Rnf135 | GRCm38.p3 | 11:80192164 | AGATTTGTGGTATCG[C/T]CTGCTCTCACAGCCA | 71956 |
rs28227525 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf135 | GRCm38.p3 | 11:80192139 | GAATAGCCGTAATCC[C/T]GTGGAACCGAGATTT | 71956 |
rs28227526 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Rnf135 | GRCm38.p3 | 11:80191931 | GGTCTTAAGACACTC[C/T]TGGCTGGCCAGTGGT | 71956 |
rs28227527 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Rnf135 | GRCm38.p3 | 11:80191572 | ATTTTAGGCCAGCAC[A/G]TACAGGAGCCCAGTG | 71956 |
rs28227528 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Rnf135 | Mm_Celera | 11:80191456 | CACTCTATTTTAGTT[A/G]GCTCCCTTCACACAA | 71956 |
rs28227529 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Rnf135 | GRCm38.p3 | 11:80191311 | CCTTACCTGCCTAGC[A/G]GTGCATGGTAGCTCC | 71956 |
rs28227530 | snp | C/G/T | 0.18 | 0.24 | intron-variant | Rnf135 | GRCm38.p3 | 11:80190676 | TTTCAGTATGTAATT[C/G/T]GAGCTGCCTTTGAAC | 71956 |
rs28227531 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf135 | Mm_Celera | 11:80190251 | TCTTCACTGCCAAGC[C/T]AACTCTCCAGCCTCA | 71956 |
rs28227532 | snp | C/T | 0.18 | 0.24 | intron-variant | Rnf135 | GRCm38.p3 | 11:80187082 | CTGGCCTTTTGCAAG[C/T]TGGGTAAGGGTCCCT | 71956 |
rs28227533 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf135 | GRCm38.p3 | 11:80186846 | TCCATCGGGAAGGAA[A/G]GACCCTGACTGAATT | 71956 |
rs28227534 | snp | A/G | 0.18 | 0.24 | intron-variant | Rnf135 | GRCm38.p3 | 11:80185466 | ACTACTTTCAGTTTC[A/G]TATTTTCAGGGCTGC | 71956 |
rs28227535 | snp | A/C | 0.18 | 0.24 | intron-variant | Rnf135 | Mm_Celera | 11:80185011 | TTAGGTCAGAAAGCG[A/C]CGCACTGAGACCACC | 71956 |
rs28227536 | snp | C/T | 0.18 | 0.24 | missense | Rnf135 | GRCm38.p3 | 11:80184128 | GTCGGAAGGGTCCCT[C/T]GACAAAGCCCAAGCT | 71956 |
rs28227537 | snp | C/T | 0.18 | 0.24 | utr-variant-5-prime | Rnf135 | GRCm38.p3 | 11:80183915 | CTGGCTGTCGCCTAA[C/T]TATGGCGGCCGTTTG | 71956 |
rs28227538 | snp | C/T | 0.165289 | 0.235211 | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182598 | GAGTGGGTCATAACA[C/T]CTTTGGCAAACTCCT | 71956 |
rs28227539 | snp | C/T | 0.18 | 0.24 | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182560 | TGACTGCTGAGGTAC[C/T]TGCTAGAGCAGTGAT | 71956 |
rs28227540 | snp | A/G | 0.21875 | 0.248039 | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182408 | GTGCCTTCATGCCTG[A/G]TGAGGTCCTCTGAAT | 71956 |
rs28227541 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80181831 | CCCAAGGTACTTGTT[A/C]GGTGCTTCTTTGTTT | 71956 |
rs211877884 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80198509 | AAGCATACAGACATA[A/T]AAATTAAAGAAGTAA | 71956 |
rs211892556 | snp | C/T | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199565 | AAAAGTCTAGCCCAA[C/T]AGTATAGCTGGGTGA | 71956 |
rs212081963 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190889 | GTTAGCAGTTGAGTC[C/T]TGTAGCAAACCCCAG | 71956 |
rs212103915 | snp | G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185707 | AGGGCAGGAGAGTTC[G/T]ACCCTGAGCAGTAAC | 71956 |
rs212254645 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183573 | ACCAGAAGAGGGCAT[C/T]AGATCCCATTTTTGT | 71956 |
rs212532709 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80186315 | CCCTTACATAGACAT[A/G]CATGTAGTCAAAACA | 71956 |
rs212857816 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80196114 | GTTAGCAAGGAGTTT[C/T]GGGTTCTGTAGGGGA | 71956 |
rs212914727 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189046 | GTATTTGCATCTACC[G/T]ATGGAGTGCTGGGAT | 71956 |
rs213608436 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196274 | TGGATGCTGAAGTGG[A/G]CATTTCTGGTTTCTT | 71956 |
rs213666628 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80197043 | GGTGGGTTCCCCCAG[C/G]ACTGCATAAACCAGG | 71956 |
rs213681442 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80198232 | GATTTATTGGTAAAT[A/G]TCACACCAAAAAATG | 71956 |
rs213818618 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80189868 | TAGGCTGGAGAGATG[A/G]CTCAGCGGTTAAGAG | 71956 |
rs213992318 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190179 | CTATAGATGGGTGTG[A/G]CCCATCATGTGGGTA | 71956 |
rs214300959 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190421 | TCTCTTTGTCCATTG[C/T]AGGTTCCAGGAATCT | 71956 |
rs214409469 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193248 | GTGAGTTTGAGTCCA[A/G]TTTGGGCTACAAAGC | 71956 |
rs214558501 | snp | A/G | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80184237 | TGAACCCGCCCCCGC[A/G]CCGCGTTCTGCGCCC | 71956 |
rs214617635 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194433 | ATCATCATCGGTGTT[A/G]CAATCCAGCAGCAAC | 71956 |
rs214627933 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194849 | CAGCGTCGTCCACTG[A/T]CTGCTGGGTAATATT | 71956 |
rs214705323 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80192660 | TCTTAAGATTTCATA[A/C]GCCTTGTGTGTTTTA | 71956 |
rs214820071 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194256 | GAATCAGCAGTGGCC[A/G]CTCAGATTCACTCAC | 71956 |
rs214825662 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184420 | TTTTGGAGTGGCTTG[C/T]CCCACAGGGCCAGAG | 71956 |
rs214865749 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80185644 | CTGATGCAAACTGCA[A/G]GAGGTTTTATTATCA | 71956 |
rs215079728 | snp | A/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186480 | CCTCTGCCTCCCAAG[A/T]GCTGGGATTAAAGGC | 71956 |
rs215346395 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80195053 | TGATTGTGTCAGCTG[A/G]GTAGGGGCGAGCTGA | 71956 |
rs215402470 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195993 | GTTCTGGATTTGAGG[G/T]TGCCGCAATCCCCTG | 71956 |
rs215537075 | in-del | -/AC | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80181923 | AAGAGATTCCACATA[-/AC]ACACATGCACACACA | 71956 |
rs215720921 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80194162 | AGCCCACCACCCACC[A/G]GAGGTAGTGGAAAGG | 71956 |
rs215756219 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190978 | ACCAAATGGCCTGAG[A/G]CCGCAGCAGCAGCAA | 71956 |
rs215765514 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80191878 | TCTGGAGAATCTGAA[C/T]TTGGTGCTATGTGAG | 71956 |
rs216145964 | in-del | -/AA | | | intron-variant | Rnf135 | Mm_Celera | 11:80193595 | AAAACAAACACAAAC[-/AA]ACAAACAAAAAACCC | 71956 |
rs216263629 | in-del | -/AAAA | | | intron-variant | Rnf135 | Mm_Celera | 11:80193065 | AAAAAAACATAAAAT[-/AAAA]AGGATCTTATAGACT | 71956 |
rs216331700 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193388 | TTTCTAGAAGAACTG[C/G]GGTTGATCTTCAATA | 71956 |
rs216546415 | snp | A/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183448 | TTGAACTTCAGACCT[A/T]CGGAAGAGCAGTTGG | 71956 |
rs216708731 | snp | A/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183201 | TTCCAATTTTTTGTT[A/T]GGTATTTTCTTCATT | 71956 |
rs216780112 | in-del | -/TTTTTTTTTT | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183306 | AAGACTGAGGCTGTC[-/TTTTTTTTTT]TTTTTTTTTTTTTTA | 71956 |
rs217047332 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182593 | TCAATGAGTGGGTCA[C/T]AACACCTTTGGCAAA | 71956 |
rs217052589 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80185685 | GATGAACTCCTCAAC[A/G]CCCTGCAGGGCAGGA | 71956 |
rs217289970 | snp | A/G | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182882 | GCTATCTTCAGACAC[A/G]CCAGAAGAAGGCATC | 71956 |
rs217410865 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190556 | TAGCCTTCAACGTGA[A/G]CTCCTCCTAGCCTCC | 71956 |
rs217721160 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192540 | GTCCCTGTGGCATGT[C/G]TGTGTTTTCCCACTA | 71956 |
rs217723971 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80191989 | GGAGGCAGAGGCAGG[C/T]GGATTTCTGAGTTCG | 71956 |
rs218321564 | snp | C/T | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80199045 | CGCCTTCTGGCTGTA[C/T]GGCTTAAGTCCTGGA | 71956 |
rs218386343 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193470 | CTGCCTGGATGTGAT[A/G]GTGAATGCCTTTAAT | 71956 |
rs218448520 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194409 | GCAGTGTCAGAATAG[C/G]AAACACAAATCATCA | 71956 |
rs218537356 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186954 | CCAGGGGGTATCTGG[A/G]TGATGCTATGATTGG | 71956 |
rs218591501 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190531 | TGGAATTTTGTTGTG[C/T]TGTCCAGTCTAGCCT | 71956 |
rs218654596 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184908 | GACCTCTGTACCCAC[C/T]CACTAAGCAATAACA | 71956 |
rs218936733 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197560 | AAGGCTAAGAGGGTT[C/T]AGAGTCCTAGATTCT | 71956 |
rs218959476 | in-del | -/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182820 | AAGAGTAGTTGGTTA[-/T]TTTTTTTTTAAAGAT | 71956 |
rs218961938 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80186046 | AGTCGGGGTCCCACA[G/T]ATATATATCACTTTC | 71956 |
rs219002714 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80196360 | TTTGCTGAGGCAGAC[A/G]CTTGAGAAAGCCAGC | 71956 |
rs219046946 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80198401 | CCCTCTCGGTGCCTC[A/C]CAATGTTCTGGAATT | 71956 |
rs219378049 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194654 | AACATCACGTATCTT[C/T]TCGTGGGTCTTGCAT | 71956 |
rs219433056 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80195366 | GAGTTGGCAACAGGT[A/G]CCTTTAACCATTGAA | 71956 |
rs219446488 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189600 | GAAGACAGCTTTCAG[C/T]TAGAGCTGTATGGGA | 71956 |
rs219629819 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80194765 | AAGTGGCAGGAAGCC[A/G]CTCAACACCACCAGG | 71956 |
rs219704498 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80197773 | ATTAGTTACCTCTTA[A/G]GGCTTGGTTCTCCTA | 71956 |
rs219795561 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80197674 | GTATATATATACTGT[A/G]TTAGCCCAGGCTAGG | 71956 |
rs219859225 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80189951 | AGTTCACAACCATTC[C/G]TAATGAGATCAGATG | 71956 |
rs219860023 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80196438 | TCTCTTGTTTTGCTA[C/T]GTCATGCAGTACTTT | 71956 |
rs220171263 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193637 | AATAAAACAAAGCCT[A/G]TTTATACTTCATTTA | 71956 |
rs220527792 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80191096 | GATGGTTGTGAGCCA[C/T]CATGTGGTTGCTGGG | 71956 |
rs220740590 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193718 | CAGGAGGCAGAGGCA[G/T]GCGGATTTCTGAGTT | 71956 |
rs220774837 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185328 | GATTATTAACAGCCC[A/T]TTGTCTCAATCTGCT | 71956 |
rs220798026 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194480 | AATCAGCACGAGTCA[G/T]CAGGAGCAACCGTGG | 71956 |
rs220866015 | in-del | -/A | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80199092 | GCAGCTAAACACATG[-/A]AGCTTCCCTCGGGGT | 71956 |
rs221104308 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195146 | CTCCTATTTTTAAGA[C/T]ATGTGATCCCTAATC | 71956 |
rs221152362 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186745 | GTGTTAGGGTTAGAA[C/T]TGCTGAAGAATGATA | 71956 |
rs221260466 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190595 | CTTGAGTTCCCCTGT[A/G]CTCTCCAGGTTGCCT | 71956 |
rs221442584 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194562 | AAGATCAGTGAAGAC[C/G]CAAGACCACCAAAGC | 71956 |
rs221458564 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194863 | GTCTGCTGGGTAATA[-/T]TTATTTCCCTTCTGA | 71956 |
rs221498866 | in-del | -/AAT | | | intron-variant | Rnf135 | Mm_Celera | 11:80190036 | ATAAATCTTTAAAAA[-/AAT]AAAAGATGTATTTAT | 71956 |
rs221521082 | in-del | -/AAAAAA | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186692 | GAGAAACCCTGTCTC[-/AAAAAA]AAAAAAAAAAAATTC | 71956 |
rs221541999 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80186002 | TGGGGAACGTCCAGG[A/G]GCTTTACCTTCTAGG | 71956 |
rs221720721 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80191013 | CTGCAGGAACAGGGA[A/G]AACACTTTGTGTGAG | 71956 |
rs221753100 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184345 | GAACCTTAAAAAGTT[C/T]ATAGCTGTATAAAGA | 71956 |
rs221890925 | in-del | -/CTC | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80199914 | ACTGCTCTTCCAGAT[-/CTC]CTGAATTCAAGTCCC | 71956 |
rs222121173 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189175 | GAGGGAGCTATATTC[C/T]GGGGTCCAAGTTTTT | 71956 |
rs222212281 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192746 | ATCAGGTAACTTGGA[C/T]TACTGTCTGTCTATT | 71956 |
rs222333215 | in-del | -/TTT | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183034 | TTTTTTCTTTTTCCA[-/TTT]TTTTTTTTTTTTTTT | 71956 |
rs222429157 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190866 | TAGGGGCAGACTTGG[C/T]CTTCTTTGTTAGCAG | 71956 |
rs222509244 | snp | G/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183808 | TAGCAGCTGGGCGGG[G/T]CGAGCTGATGGGAGG | 71956 |
rs222548189 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186512 | TGCGCCACCACGCCC[A/G]GCTCACTTATTTTTT | 71956 |
rs222607493 | in-del | -/TC | | | intron-variant | Rnf135 | Mm_Celera | 11:80184976 | CTCATAAGCTTTATG[-/TC]TCTGAGTTTACCTGT | 71956 |
rs222650911 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80181964 | acacacacacacacT[C/T]ATGTTTTTTAAATGA | 71956 |
rs223122748 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190645 | TGGCTGGATCTCTAT[C/T]TTAGGCCGGCCTTGA | 71956 |
rs223194215 | in-del | -/CTT | | | intron-variant | Rnf135 | Mm_Celera | 11:80194635 | GTCCTATTTATACTC[-/CTT]CTAAACATCACGTAT | 71956 |
rs223197400 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193020 | CCACCACCTTATACC[A/T]CATACACAGATACCA | 71956 |
rs223333571 | snp | C/T | | | missense, intron-variant | Rnf135 | Mm_Celera | 11:80189312 | TCAAGAGCCTTCAAA[C/T]GCAAAGACCCAACTT | 71956 |
rs223369778 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80189936 | CAACAACCACATGGT[A/G]GTTCACAACCATTCC | 71956 |
rs223987743 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190581 | GCCTCCTGACTACTC[C/T]TGAGTTCCCCTGTGC | 71956 |
rs224173330 | snp | C/G | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80184216 | GGTCGAGGCTGGCTC[C/G]GAGCCTGAACCCGCC | 71956 |
rs224379972 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80198157 | AAGAAAATAAGAACA[G/T]GAATGGGATGTTGAT | 71956 |
rs224428405 | snp | A/C | | | synonymous-codon, intron-variant | Rnf135 | GRCm38.p3 | 11:80189358 | CAATGCACAAGGCAC[A/C]CCACCCACGGTAAGT | 71956 |
rs224500819 | snp | A/G | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182566 | CTGAGGTACCTGCTA[A/G]AGCAGTGATTCTCAA | 71956 |
rs225014973 | in-del | -/A | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80200040 | TTAAAAAAAAAAAAG[-/A]AAAAAAGAAAAAAAA | 71956 |
rs225360252 | snp | A/C | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183559 | CTGTCTTCGGACACA[A/C]CAGAAGAGGGCATTA | 71956 |
rs225469907 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80193365 | ATTATCTGTAAAAAG[A/C]ACTTGTTTTTCTAGA | 71956 |
rs225535610 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194064 | GTGAGCTGATGTTTA[C/T]TGGAGCAGGACTGAT | 71956 |
rs225636656 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195961 | TTTGTGGTACTGACA[C/T]GGCGGGGTTTGTGAG | 71956 |
rs225701660 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196676 | CCCCAAAGAACAACT[A/G]CTAAACAGGTCCACA | 71956 |
rs226003912 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192926 | CAGGATTAGTGAAGG[A/G]CCCTGTCTCACGGGA | 71956 |
rs226381904 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195563 | AGCCACTGTGTAGGT[G/T]CTGGGGACCAAACAA | 71956 |
rs226691021 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192505 | ACAGGATCCTTCCTG[C/T]GTCCTTCCTGACCAC | 71956 |
rs226802119 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193163 | AAATACATTAAATAA[A/G]TAATAGTTGGGTGTG | 71956 |
rs226824664 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183254 | AAGTCTCCTATACCC[C/T]CCCCCCAGATTTACT | 71956 |
rs226853181 | snp | A/G | | | utr-variant-5-prime | Rnf135 | Mm_Celera | 11:80183903 | TAAGGGTGCTTCCTG[A/G]CTGTCGCCTAATTAT | 71956 |
rs226919402 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196348 | GTGAAAGGATGTTTT[C/G]CTGAGGCAGACACTT | 71956 |
rs227115043 | in-del | -/AAACAAAC | | | intron-variant | Rnf135 | Mm_Celera | 11:80193309 | AAACCCTGTCTTGAA[-/AAACAAAC]AAACAAACAAACAAA | 71956 |
rs227202289 | snp | A/G | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80200207 | GGATTAAAGGCATGC[A/G]CCACCACTGCCCGGC | 71956 |
rs227544767 | snp | A/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80187256 | TCATCACAtttcttt[A/T]atttttttttaatta | 71956 |
rs227593069 | snp | A/G | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80198946 | GCTGGACCTGGAGTC[A/G]GGGGAGCTTGCCTTC | 71956 |
rs227685047 | snp | A/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80187125 | AGCAGTGTTCCAGTA[A/T]CTGACTTGCTCAGTT | 71956 |
rs227737350 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194321 | ATCCAGAAGAAAGCA[C/T]GAGACTCTGCTATAT | 71956 |
rs227785528 | snp | C/T | | | missense | Rnf135 | Mm_Celera | 11:80196911 | CTGCCTGACCAGAGG[C/T]GTCCTGCACCCAGGA | 71956 |
rs227959412 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190704 | AACTCCTGACCCTCC[G/T]TTCTTGTTACTCTGT | 71956 |
rs228081708 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80198341 | TGGCTCAGTGGTTAA[A/G]AGCACTGGCTGCTCT | 71956 |
rs228114071 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190447 | AATCTATCTCAGGTC[A/G]TCAGACTTGTGCAAC | 71956 |
rs228155841 | snp | C/T | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199218 | CTTGGGACGTGGAGG[C/T]AGGTGGATCACTGCA | 71956 |
rs228459501 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193222 | CAGGAGGCAGAGGCA[A/G]GTGGATCTCTGTGAG | 71956 |
rs228489616 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190390 | GGAGGTCAGAGCACA[A/G]CTTTCCAGAGTCCAT | 71956 |
rs228697011 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182929 | GGTTGTGAGCCACCC[C/T]GTGGTTGCTGGGCAT | 71956 |
rs228805880 | in-del | -/A | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186693 | GAGAAACCCTGTCTC[-/A]AAAAAAAAAAATTCT | 71956 |
rs228905236 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185654 | CTGCAAGAGGTTTTA[C/T]TATCAGCTAGCTGAG | 71956 |
rs228910170 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194728 | CTTCCTCTTCACTCT[G/T]CCAATAGGCCCAAGT | 71956 |
rs229023780 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80186225 | TAGTGCTCTTCCAGA[A/G]GACCTGGGTTCAAGT | 71956 |
rs229044863 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193851 | AGTTCCTCAGTTGGC[A/T]TTCATTTCATTGTTC | 71956 |
rs229293355 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194794 | GGAAGTCATGACAAA[C/G]GATGACCAGTAAAGA | 71956 |
rs229329745 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80186316 | CCTTACATAGACATA[C/T]ATGTAGTCAAAACAC | 71956 |
rs229439508 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80189630 | AGATGAGTGTACCGC[A/G]TCTCATGCTTTACCA | 71956 |
rs229574441 | in-del | -/AGT | | | intron-variant | Rnf135 | Mm_Celera | 11:80184461 | GATCCCATCACAAAC[-/AGT]AGTTAAAAATCCAAG | 71956 |
rs229871652 | in-del | -/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80186384 | TTGTTTTTGTTTTTT[-/C]GAGACAAGGTTTTTC | 71956 |
rs229999886 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80186132 | GACTACTAATACAAT[A/G]TACATTATCTTATAA | 71956 |
rs230357096 | snp | C/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185603 | TGAGCTGGCCAGCAC[C/G]TCAATGACTTGAGAG | 71956 |
rs230449256 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80188835 | GAAGCCACAACATTT[C/T]TTTAATCACAGCACT | 71956 |
rs230494122 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189181 | GCTATATTCCGGGGT[C/T]CAAGTTTTTGGGAAC | 71956 |
rs230529575 | snp | A/G | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183454 | TTCAGACCTTCGGAA[A/G]AGCAGTTGGGTGCTC | 71956 |
rs230630895 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183592 | TCCCATTTTTGTTGC[C/T]ACTTCATAACTGTAA | 71956 |
rs230877711 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185779 | TTGGGAGGAGAGTTG[A/G]CTACAGCTCCTTTCT | 71956 |
rs230925620 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183151 | TCGAACTCAGAAATC[C/T]GCCTGCCTTAAAGGC | 71956 |
rs231137112 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80191743 | GTGCCTCCCAGTTAA[A/G]AGCCCTGGGTTAGAC | 71956 |
rs231561679 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194471 | CCTCCGCCGAATCAG[C/T]ACGAGTCAGCAGGAG | 71956 |
rs231594078 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194859 | CACTGTCTGCTGGGT[A/T]ATATTTATTTCCCTT | 71956 |
rs231813756 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80192050 | AGACAGTCAGGACTA[C/T]ACAGAGAAACCTTGT | 71956 |
rs231895029 | snp | A/G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80198540 | AAAACGTAACTGACC[A/G/T]TGGTGTTTACTCCTC | 71956 |
rs231951414 | snp | C/T | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80199798 | TCGTGTCCTTTGAAG[C/T]ATATATTGACCTTCA | 71956 |
rs232179154 | snp | C/T | | | synonymous-codon | Rnf135 | GRCm38.p3 | 11:80198760 | GGACACTAGGAACTG[C/T]AGCCACTGGGCCATC | 71956 |
rs232455067 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186554 | AGGATAAGACTCTAA[A/G]TTTGCTGGGTGGTCG | 71956 |
rs232590270 | snp | C/G | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80200058 | AAAAGAAAAAAAAAA[C/G]TCCCTTTTTTGCTTT | 71956 |
rs232615601 | in-del | -/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194768 | GGCAGGAAGCCGCTC[-/G]AACACCACCAGGAAG | 71956 |
rs232646485 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190981 | AAATGGCCTGAGGCC[A/G]CAGCAGCAGCAAGGT | 71956 |
rs232657871 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80191919 | TGCACTGACCTTGGT[C/T]TTAAGACACTCCTGG | 71956 |
rs232808589 | snp | A/C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190195 | CCCATCATGTGGGTA[A/C/T]TGGGCATTGAACTCA | 71956 |
rs233362312 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192678 | CTTGTGTGTTTTATC[A/G]GTTATTACAGCTGCA | 71956 |
rs233919000 | snp | C/T | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80198805 | GGGCATGAAGCGGGA[C/T]GGGATGCTGGGAAGG | 71956 |
rs233949854 | in-del | -/TTT | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182430 | CTCTGAATTTACTGA[-/TTT]TTTTTTTTTAATTCC | 71956 |
rs234040553 | snp | A/T | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199313 | CCCAATTTTAAAGTT[A/T]TTCTTTTTGGGAGTG | 71956 |
rs234052853 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190875 | ACTTGGCCTTCTTTG[G/T]TAGCAGTTGAGTCCT | 71956 |
rs234099401 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197924 | TCTGAAGTGTGGTTC[C/T]GTAGTACAGCATTTG | 71956 |
rs234107387 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185369 | ACTGAAACTTTTCTA[C/T]TTCCAAGGTTTTTAT | 71956 |
rs234289171 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192877 | GTGGCTGGAAGAATG[A/G]GATCACTGTGACTTA | 71956 |
rs234388757 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184515 | CACACTTGTATAGTT[C/T]TAGTTTTTCCCAGCC | 71956 |
rs234611889 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80195295 | AGCTTGTATGTGGGG[A/G]GAAATCAGGACAACT | 71956 |
rs234677828 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196294 | TCTGGTTTCTTTGGA[C/G]TGAGTTGAGTCACTT | 71956 |
rs234741129 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80197136 | TTTGAGACCAGCCTG[C/G]GCTATCCGAGACTCA | 71956 |
rs234776488 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189874 | GGAGAGATGGCTCAG[C/T]GGTTAAGAGCACTAA | 71956 |
rs234831412 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189720 | GAAGTTTCGAGTAGG[C/T]TGGGATCCATCCTTC | 71956 |
rs235157720 | snp | A/G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80196786 | CTAAATAAAGTAGGC[A/G/T]TTGTAAAAACCTAAG | 71956 |
rs235198587 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192033 | CTACAGAGTGAGTTC[C/T]AAGACAGTCAGGACT | 71956 |
rs235242345 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190559 | CCTTCAACGTGAACT[C/T]CTCCTAGCCTCCTGA | 71956 |
rs235296755 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80193033 | CCACATACACAGATA[C/T]CACACACACATGCAC | 71956 |
rs235315095 | in-del | -/TA | | | intron-variant | Rnf135 | Mm_Celera | 11:80195812 | ACCTGTGTGTGCATG[-/TA]CACACACACGCACAA | 71956 |
rs235465666 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189938 | ACAACCACATGGTAG[C/T]TCACAACCATTCCTA | 71956 |
rs235521247 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190027 | ATAAATAAATAAATC[-/T]TTTAAAAAAATAAAA | 71956 |
rs235602111 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193511 | AGGAGGCAGAGGCAG[A/G]TGGATCTCTTGAGTT | 71956 |
rs235748813 | snp | A/C | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182860 | TATTATATGTAAGTA[A/C]ACTGCAGCTATCTTC | 71956 |
rs235901926 | snp | C/G | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183502 | TCACCAGCCCCTGAG[C/G]CTGTCTTTTAATGTC | 71956 |
rs236025495 | in-del | -/AAA | | | intron-variant | Rnf135 | Mm_Celera | 11:80193568 | AACCCTGTCTCAAAC[-/AAA]AAAAAAACAAAAACA | 71956 |
rs236092010 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80196311 | AGTTGAGTCACTTGA[-/T]TTTTTTTCTGGAAGC | 71956 |
rs236220374 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196115 | TTAGCAAGGAGTTTC[C/G]GGTTCTGTAGGGGAA | 71956 |
rs236254379 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183256 | GTCTCCTATACCCTC[C/T]CCCCAGATTTACTTA | 71956 |
rs236370695 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80185877 | GTATGTCTTCCTACA[A/G]TTATCGAATCTCTGG | 71956 |
rs236406395 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189071 | TGGGATTAAAGGCAG[C/T]AGCATCGCTTTAGCC | 71956 |
rs236689207 | in-del | -/AAAG | | | intron-variant | Rnf135 | Mm_Celera | 11:80188955 | CCTGTCTAAAAAACA[-/AAAG]AAAGAATGTAACTTA | 71956 |
rs236907188 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190895 | AGTTGAGTCCTGTAG[C/T]AAACCCCAGCTATGA | 71956 |
rs236968631 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192589 | GCTTCCTTGGGGAAG[A/G]CCAGTCCTCTTCCCT | 71956 |
rs237493531 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194418 | GAATAGCAAACACAA[A/G]TCATCATCGGTGTTA | 71956 |
rs237661719 | in-del | -/CA | | | intron-variant | Rnf135 | Mm_Celera | 11:80195856 | TATATATGCACATAT[-/CA]CACACATGAAAATGG | 71956 |
rs237680963 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193685 | GGCATGGTGGCGCAC[A/G]CCTTTAATCTCAGCA | 71956 |
rs237735315 | snp | G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186210 | GTGGTTAAGAGCACT[G/T]AGTGCTCTTCCAGAG | 71956 |
rs238044490 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80196473 | GTCTTCAGTTGTAGC[C/T]CTGTAGAGAGAAACA | 71956 |
rs238107289 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197702 | AGGTGGTCCACATGC[C/T]CCCTGAACTCCTGGT | 71956 |
rs238206570 | snp | G/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183046 | TCCATTTTTTTTTTT[G/T]TTTGGTTTTGTTTTG | 71956 |
rs238244425 | snp | A/C | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183739 | TGATTTTTCCAGGCC[A/C]AAATCCAGGCAGGTA | 71956 |
rs238270410 | in-del | -/TGT | | | intron-variant | Rnf135 | Mm_Celera | 11:80195248 | ATTTTTACTTATACA[-/TGT]TGTGGTGGTGGTAGG | 71956 |
rs238470022 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80194426 | AACACAAATCATCAT[C/T]GGTGTTACAATCCAG | 71956 |
rs238490507 | snp | G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186489 | CCCAAGTGCTGGGAT[G/T]AAAGGCATGCGCCAC | 71956 |
rs238641410 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195009 | TTTGTTCTTTGGAGA[C/T]AGGGCCCAGAGCCTG | 71956 |
rs238785205 | snp | A/C | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190985 | GGCCTGAGGCCGCAG[A/C]AGCAGCAAGGTTCTG | 71956 |
rs238924756 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190612 | TCTCCAGGTTGCCTT[A/G]TTTGCTTTTGTTTTA | 71956 |
rs239387052 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192131 | TTGATTATGAATAGC[C/T]GTAATCCCGTGGAAC | 71956 |
rs239394390 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80198407 | CGGTGCCTCCCAATG[G/T]TCTGGAATTCCAGTT | 71956 |
rs239843193 | snp | A/G | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199177 | AGGGAGACTGGATAT[A/G]GTAGTGCATACCTAT | 71956 |
rs239868438 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80189719 | GGAAGTTTCGAGTAG[A/G]CTGGGATCCATCCTT | 71956 |
rs240233757 | in-del | -/AAAT | | | intron-variant | Rnf135 | Mm_Celera | 11:80192081 | TCAAGGGGAAAAAAA[-/AAAT]AAAGACGCTCCTGGC | 71956 |
rs240352383 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80196719 | TACTAACCATCTTTC[C/T]CCCCAAACTTTGGTT | 71956 |
rs240363579 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197782 | CTCTTAAGGCTTGGT[C/T]CTCCTATCTTGCCAA | 71956 |
rs240420336 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190172 | ATCAAAGCTATAGAT[A/G]GGTGTGGCCCATCAT | 71956 |
rs240485618 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195997 | TGGATTTGAGGGTGC[C/T]GCAATCCCCTGGAAC | 71956 |
rs240647307 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80191507 | TGCTTGAAATACTCT[A/G]GTAATGTCTGACTTA | 71956 |
rs240707598 | snp | A/G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80192238 | CAGTTAACCTTGTAT[A/G/T]TGTTTGACTAAAGGA | 71956 |
rs240898001 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80191662 | AGAGGAGAGAAAGAA[A/G]AAAGGAATGGTACCA | 71956 |
rs240997955 | snp | A/G | | | missense | Rnf135 | Mm_Celera | 11:80193943 | CTGGTGACCTTCAGT[A/G]TATCTCAGAAGAAAA | 71956 |
rs241034221 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194655 | ACATCACGTATCTTC[C/T]CGTGGGTCTTGCATC | 71956 |
rs241088810 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195390 | CATTGAACCATCTCT[C/T]GGCTCCCTGCTTTCA | 71956 |
rs241158458 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186780 | AGACTCAAGTAGTAT[A/G]CAAAAGTATAGAGTG | 71956 |
rs241198120 | snp | C/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186944 | GGTTCTTTCACCAGG[C/G]GGTATCTGGATGATG | 71956 |
rs241445815 | in-del | -/CCA | | | intron-variant | Rnf135 | Mm_Celera | 11:80193002 | TGTGTACATATACCC[-/CCA]CCACCACCTTATACC | 71956 |
rs241484895 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193186 | TGGGTGTGGTAGAAC[C/G]TGCCCCTTAGTCTCA | 71956 |
rs241494682 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193719 | AGGAGGCAGAGGCAT[G/T]CGGATTTCTGAGTTT | 71956 |
rs241675765 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80185904 | CTGGCTGTAAGGCAC[A/G]GAAACAAAAGGGCTT | 71956 |
rs241762561 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184922 | CTCACTAAGCAATAA[C/T]ACCTGATTCCTGTCC | 71956 |
rs241768030 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80187061 | CTTGGCCACAAGCTT[A/G]GCTAACTGGCCTTTT | 71956 |
rs241811518 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186995 | GCTTCAAGCATACTT[A/G]TCTAACTATTCTTGC | 71956 |
rs242484691 | snp | A/G | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80200220 | GCGCCACCACTGCCC[A/G]GCTGGTATACAGATT | 71956 |
rs242868797 | in-del | -/TA | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182208 | CTTTTTCTTTTTCTT[-/TA]TTTCTTTTTCTTTTT | 71956 |
rs243155347 | in-del | -/A | | | intron-variant | Rnf135 | Mm_Celera | 11:80193143 | GGTCTCTAGCACTAT[-/A]AAAAAAATACATTAA | 71956 |
rs243175984 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195117 | CTGTAACATAGGCCC[C/T]GAGTAAAGCAAAACT | 71956 |
rs243285833 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime | Rnf135 | Mm_Celera | 11:80183870 | TTGCCGGGGAAGTTA[A/G]TAGGACAAGGCGGAA | 71956 |
rs243334385 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185038 | ACCACTCCCATTCAA[-/T]AGGCAAGAGTGTTTT | 71956 |
rs243525788 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80192390 | CAACATCAAACAATA[C/T]TAGACATTATTAGAT | 71956 |
rs243553252 | in-del | -/CTC | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80181849 | GCTTCTTTGTTTCTT[-/CTC]CTTTCAGTGGAATGA | 71956 |
rs243581452 | snp | G/T | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80199853 | TGTTGCTTAGCAATT[G/T]TCATGTAATAATAAT | 71956 |
rs243587632 | in-del | -/C | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182266 | TTTTTTTCTTTCTTT[-/C]TTTTTTTTGAGTCAG | 71956 |
rs243709241 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80184362 | TAGCTGTATAAAGAA[A/G]TACAAAAGCCCAATG | 71956 |
rs243744789 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80191765 | GGGTTAGACTGCAGT[A/G]AACGGTTTCAGCAAA | 71956 |
rs243756164 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80192435 | GATCTGAACTGTGGC[A/C]GTGTCTGTCTGTTTG | 71956 |
rs243815167 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190096 | CTGCTTCTTTTGTAT[A/G]TGCACCGTGTGCATG | 71956 |
rs243912987 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194578 | CAAGACCACCAAAGC[A/G]TCACAAGGCTAGTTC | 71956 |
rs244526788 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80191159 | GTGCTCTTAACCGCC[A/G]AGCCATCTCTCCAGC | 71956 |
rs244538721 | snp | A/G | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182583 | GCAGTGATTCTCAAT[A/G]AGTGGGTCATAACAC | 71956 |
rs244616419 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185664 | TTTTATTATCAGCTA[A/G]CTGAGGATGAACTCC | 71956 |
rs244722375 | in-del | -/TA | | | intron-variant | Rnf135 | Mm_Celera | 11:80190030 | AAATAAATAAATCTT[-/TA]AAAAAATAAAAGATG | 71956 |
rs244850686 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80189185 | TATTCCGGGGTCCAA[A/G]TTTTTGGGAACCAGA | 71956 |
rs245148297 | snp | A/G | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80181984 | TTTTTAAATGACAGA[A/G]CCTCATGTGGTCCAG | 71956 |
rs245180485 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192954 | GGAATAAGGTGGAGA[A/G]TGACAGAGCAGGACA | 71956 |
rs245614880 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80188920 | GTGAGTTCCAAGACA[A/G]TCAGGACTTTGTAGA | 71956 |
rs245778083 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197005 | ATATAACTCCATAGA[C/T]AGTACCATGCCAGCA | 71956 |
rs245830253 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80198231 | CGATTTATTGGTAAA[C/T]GTCACACCAAAAAAT | 71956 |
rs246106480 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80186168 | GTAGTATGTAAAAGT[A/T]TGTTTGGGGGCTGGA | 71956 |
rs246152117 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80185174 | TATCAAACATTAGGT[A/G]ATCTAAAACTTCATT | 71956 |
rs246211277 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195988 | TGAGTGTTCTGGATT[C/T]GAGGGTGCCGCAATC | 71956 |
rs246256102 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80188882 | CAAATCTCGGTGAGT[C/T]CCAGGCCAGCCTGGT | 71956 |
rs246289368 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189624 | TATGGGAGATGAGTG[C/T]ACCGCGTCTCATGCT | 71956 |
rs246409927 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80198349 | TGGTTAAGAGCACTG[C/G]CTGCTCTTCAAGAGG | 71956 |
rs246523275 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189419 | GCTCACGGTTAAGAG[C/T]ACTGACTGCTCTTCC | 71956 |
rs246609452 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190856 | AGTAGTTCTTTAGGG[A/G]CAGACTTGGCCTTCT | 71956 |
rs246624713 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182502 | CCAGAGTGCAGCTCC[C/T]TGGGGAGGTGGATCC | 71956 |
rs246646362 | snp | C/G | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80199950 | AACCACATGGTGGCT[C/G]ACAACCATCTATAAT | 71956 |
rs246815256 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189045 | AGTATTTGCATCTAC[C/T]GATGGAGTGCTGGGA | 71956 |
rs246830138 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185903 | TCTGGCTGTAAGGCA[C/T]AGAAACAAAAGGGCT | 71956 |
rs246886633 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80189409 | TGGAGAGATGGCTCA[A/C]GGTTAAGAGTACTGA | 71956 |
rs246934636 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193380 | CACTTGTTTTTCTAG[A/G]AGAACTGCGGTTGAT | 71956 |
rs246941078 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189709 | ATGAGTTCATGGAAG[C/T]TTCGAGTAGGCTGGG | 71956 |
rs247090346 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190727 | TACTCTGTAGGCATA[A/G]TTTTTTTGCAACCTA | 71956 |
rs247129714 | in-del | -/GGGTA | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80187025 | CTTCATGCCAAGAAG[-/GGGTA]GGGTAGCTCTAGACC | 71956 |
rs247297732 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192506 | CAGGATCCTTCCTGC[A/G]TCCTTCCTGACCACA | 71956 |
rs247307754 | snp | A/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182830 | GGTTATTTTTTTTTT[A/T]AAGATTTATTTATTT | 71956 |
rs247870779 | snp | C/T | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80198964 | GGAGCTTGCCTTCTA[C/T]GCAGTGGCCGATCAC | 71956 |
rs248296014 | in-del | -/AAAAA | | | intron-variant | Rnf135 | Mm_Celera | 11:80193807 | CTGTCTCGAAAAACC[-/AAAAA]AAAAAGAAAAAAGAG | 71956 |
rs248362432 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80196397 | TGGGAAGAATACAGG[-/T]AGAACCGTACAGACA | 71956 |
rs248381574 | in-del | -/TA | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183015 | CAGCCCTGATTTACT[-/TA]TTTTTTTTTCTTTTT | 71956 |
rs248569843 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80195944 | CTTCCCTCCAATGGC[A/G]GTTTGTGGTACTGAC | 71956 |
rs248587220 | snp | G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190583 | CTCCTGACTACTCTT[G/T]AGTTCCCCTGTGCTC | 71956 |
rs248908942 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183461 | CTTCGGAAGAGCAGT[C/T]GGGTGCTCTTACCCA | 71956 |
rs249057452 | in-del | -/AAAAA | | | intron-variant | Rnf135 | Mm_Celera | 11:80193567 | AACCCTGTCTCAAAC[-/AAAAA]AAAAAAAAAACAAAA | 71956 |
rs249064496 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185572 | CCGAAGCTGTGCCTC[C/T]CCTCAAGTCCTGGGA | 71956 |
rs249369521 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197734 | TTGATGCCAGCATTT[C/T]TTTAGATAGCTATGC | 71956 |
rs249378729 | snp | C/T | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80198604 | GACCCTCTCCTATAA[C/T]CTGGAGGTTTCCAAC | 71956 |
rs249440717 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195953 | AATGGCGGTTTGTGG[C/T]ACTGACACGGCGGGG | 71956 |
rs249549234 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190352 | TGTGTGTTGAGAGGG[C/T]GTGTGTGCAGGGTAG | 71956 |
rs249774823 | snp | A/G | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199458 | ATAAGAAGGACTTCG[A/G]ACCATTCCCTATGGC | 71956 |
rs249797817 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195652 | TTTTCATTTCTGAGA[C/T]GAGGTTCCCAGAGCA | 71956 |
rs249843272 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190884 | TCTTTGTTAGCAGTT[C/G]AGTCCTGTAGCAAAC | 71956 |
rs250478743 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80198107 | TGACTATGTTTTGTG[A/G]GATTCAGAGATAACT | 71956 |
rs250566915 | snp | C/G | | | synonymous-codon | Rnf135 | GRCm38.p3 | 11:80196898 | TTCCTTGTGCCTGCT[C/G]CCTGACCAGAGGCGT | 71956 |
rs250656017 | snp | A/G | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182410 | GCCTTCATGCCTGAT[A/G]AGGTCCTCTGAATTT | 71956 |
rs250673815 | snp | A/C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80191030 | ACACTTTGTGTGAGT[A/C/T]CACTGTAGCTGTCTT | 71956 |
rs250683794 | snp | A/G | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183481 | GCTCTTACCCACTGA[A/G]CCATCTCACCAGCCC | 71956 |
rs251166313 | snp | A/C | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80187162 | AGCAGAAACTCAGAC[A/C]TGGTTTCCTAAACTG | 71956 |
rs251282289 | in-del | -/TA | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80200027 | AACAAGTAAATCTTT[-/TA]AAAAAAAAAAAAGAA | 71956 |
rs251474058 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192137 | ATGAATAGCCGTAAT[C/T]CCGTGGAACCGAGAT | 71956 |
rs251523744 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192724 | TACTCAGGGGGACAG[A/T]GAAGGTATCAGGTAA | 71956 |
rs251661439 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190413 | GAGTCCATTCTCTTT[A/G]TCCATTGCAGGTTCC | 71956 |
rs251897879 | in-del | -/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196404 | AATACAGGTAGAACC[-/G]TACAGACAGTGAAAG | 71956 |
rs251928549 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80195298 | TTGTATGTGGGGGGA[A/G]ATCAGGACAACTGGC | 71956 |
rs251993958 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196156 | AGAAAAAAGTCCCAC[A/G]GTGATAACATGGGGC | 71956 |
rs252005457 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193710 | TCAGCACTCAGGAGG[C/T]AGAGGCATGCGGATT | 71956 |
rs252015237 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194473 | TCCGCCGAATCAGCA[C/T]GAGTCAGCAGGAGCA | 71956 |
rs252062801 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185892 | ATTATCGAATCTCTG[G/T]CTGTAAGGCACAGAA | 71956 |
rs252162938 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193233 | GGCAGGTGGATCTCT[G/T]TGAGTTTGAGTCCAG | 71956 |
rs252186384 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186511 | ATGCGCCACCACGCC[C/T]AGCTCACTTATTTTT | 71956 |
rs252550237 | snp | A/C | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183613 | ATAACTGTAATTTTG[A/C]TACTCTTATGATTCT | 71956 |
rs252646881 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182881 | AGCTATCTTCAGACA[C/T]ACCAGAAGAAGGCAT | 71956 |
rs252666936 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80185997 | AAGCTTGGGGAACGT[A/C]CAGGGGCTTTACCTT | 71956 |
rs252683647 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196337 | GAAGCTGTCCTGTGA[A/G]AGGATGTTTTGCTGA | 71956 |
rs252689777 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186674 | GGACAGCCAGGGCTA[C/T]ATAGAGAAACCCTGT | 71956 |
rs252696396 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197141 | GACCAGCCTGGGCTA[C/T]CCGAGACTCAACCTG | 71956 |
rs252754418 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189920 | TCCTGAGTTCAAATC[C/T]CAACAACCACATGGT | 71956 |
rs252935631 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190635 | TTGTTTTAAGTGGCT[A/G]GATCTCTATCTTAGG | 71956 |
rs253035230 | snp | C/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190125 | TGCCTGATATAGAGC[C/G]TCAGAAGAAAGAGGA | 71956 |
rs253095373 | in-del | -/A | | | intron-variant | Rnf135 | Mm_Celera | 11:80197974 | GGATCTCATTCCCAG[-/A]ACTAGACAGGAAGGG | 71956 |
rs253241665 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194812 | TGACCAGTAAAGAAT[A/T]GTAAGGCACACCAAT | 71956 |
rs253333809 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80186352 | TACATAAAATAAAAA[A/T]AAGTAAATTTTTTTG | 71956 |
rs253607562 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194746 | AATAGGCCCAAGTCC[C/T]AGGAAGTGGCAGGAA | 71956 |
rs253982038 | snp | A/G | | | missense, intron-variant | Rnf135 | GRCm38.p3 | 11:80189345 | GATCTGGACAGGACA[A/G]TGCACAAGGCACCCC | 71956 |
rs254017859 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80198462 | TTCTGTGGGTACTGC[A/G]TGTGTGTGGTGCACA | 71956 |
rs254058304 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80196841 | TTTTGCTAATGGGGC[C/T]CCCTCTTCCCAATTA | 71956 |
rs255245320 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183178 | AGGCGTGCTCCACCA[C/T]GCCTGGCTTCCAATT | 71956 |
rs255521911 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80192904 | CTTAGTGACCATCAG[A/C]CTAGCTCAGGATTAG | 71956 |
rs255567927 | snp | A/C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192972 | ACAGAGCAGGACACC[A/C/T]GACATCCTTTTCCAT | 71956 |
rs255578111 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80184686 | TGGGGTGACTCCCTC[A/G]GCTTTCCAAGTCTGG | 71956 |
rs255745205 | in-del | -/TC | | | intron-variant | Rnf135 | Mm_Celera | 11:80191211 | CCCCAAACTGTGGTA[-/TC]TCTGAGGATTCTCCA | 71956 |
rs255797007 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185710 | GCAGGAGAGTTCGAC[C/T]CTGAGCAGTAACAGT | 71956 |
rs255803391 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182544 | TAAAGTTCTTTGGAC[C/T]TGACTGCTGAGGTAC | 71956 |
rs255862731 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184376 | AATACAAAAGCCCAA[C/T]GTGGTGGCCCCATGC | 71956 |
rs255911680 | in-del | -/AC | | | intron-variant | Rnf135 | Mm_Celera | 11:80197668 | CCCTGGTATATATAT[-/AC]ACTGTGTTAGCCCAG | 71956 |
rs256085842 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80197638 | GCATCATCAGTTACA[A/G]CTGCCTGTTTGCTCC | 71956 |
rs256114251 | in-del | -/A | | | intron-variant | Rnf135 | Mm_Celera | 11:80198082 | TACACAGGTATTGAG[-/A]AAAAAATCATGACTA | 71956 |
rs256122903 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189949 | GTAGTTCACAACCAT[C/T]CCTAATGAGATCAGA | 71956 |
rs256413460 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189730 | GTAGGCTGGGATCCA[C/T]CCTTCCCACTCTACC | 71956 |
rs256530263 | in-del | -/GTGTGTGTGTGT | | | intron-variant | Rnf135 | Mm_Celera | 11:80185796 | TACAGCTCCTTTCTG[-/GTGTGTGTGTGT]GTGTGTGTGTGTGTG | 71956 |
rs256627877 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184334 | GTTTTCTGGAGAACC[-/T]TTAAAAAGTTTATAG | 71956 |
rs256630247 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80191041 | GAGTACACTGTAGCT[A/G]TCTTCAGGCACACAG | 71956 |
rs256646834 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195958 | CGGTTTGTGGTACTG[A/T]CACGGCGGGGTTTGT | 71956 |
rs256784486 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196519 | TGTGGTCTTCCTGCG[A/G]CTTCTTGCTGCTTCT | 71956 |
rs256824881 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190594 | TCTTGAGTTCCCCTG[C/T]GCTCTCCAGGTTGCC | 71956 |
rs256938257 | in-del | -/A | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182830 | GGTTATTTTTTTTTT[-/A]AAGATTTATTTATTT | 71956 |
rs257317178 | snp | C/T | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199290 | GCTTGGACTATATGA[C/T]ATGACTGCCCAATTT | 71956 |
rs257539746 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189627 | GGGAGATGAGTGTAC[C/T]GCGTCTCATGCTTTA | 71956 |
rs257634998 | snp | A/G | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199187 | GATATAGTAGTGCAT[A/G]CCTATAACTCCAGCA | 71956 |
rs257756548 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190741 | AATTTTTTTGCAACC[G/T]ACTTTTAATAAGGGT | 71956 |
rs257938628 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80189169 | TTTATTGAGGGAGCT[A/G]TATTCCGGGGTCCAA | 71956 |
rs257984923 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192470 | TAAGACCCAAATCCT[C/T]ACAGAGCCAGAAAAA | 71956 |
rs258105939 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193045 | ATACCACACACACAT[A/G]CACTAAAAAAACATA | 71956 |
rs258209452 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194581 | GACCACCAAAGCATC[A/G]CAAGGCTAGTTCCAC | 71956 |
rs258424084 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80192069 | GAGAAACCTTGTCTC[A/G]AGGGGAAAAAAAAAA | 71956 |
rs258802851 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194668 | TCTCGTGGGTCTTGC[A/T]TCAACAAAACACCAC | 71956 |
rs258911047 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195407 | GCTCCCTGCTTTCAT[C/T]GCCTTTAGATGTATT | 71956 |
rs259023363 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185417 | GGGACCTCTCATTAT[A/T]CATGTTTCATGTAAA | 71956 |
rs259040645 | snp | C/T | | | missense | Rnf135 | Mm_Celera | 11:80198945 | GGCTGGACCTGGAGT[C/T]GGGGGAGCTTGCCTT | 71956 |
rs259266152 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196086 | TCGAAATATAGAGAT[A/G]AACACCTTCCCTGTT | 71956 |
rs259359709 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80185393 | TTTTATTTCATTTTA[-/T]TTTTTTAGGGGACCT | 71956 |
rs259408037 | snp | C/T | | | synonymous-codon | Rnf135 | Mm_Celera | 11:80184222 | GGCTGGCTCGGAGCC[C/T]GAACCCGCCCCCGCG | 71956 |
rs259750398 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190796 | CCAGCAGAGGTAGTG[A/G]AAGAGAAAAGTTATT | 71956 |
rs259776270 | in-del | -/GTAC | | | intron-variant | Rnf135 | Mm_Celera | 11:80197109 | CAAGGATATCCTTAG[-/GTAC]CTATTGAGTTTGAGA | 71956 |
rs260328225 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195132 | TGAGTAAAGCAAAAC[G/T]CCTATTTTTAAGACA | 71956 |
rs260527817 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80194394 | CAGGAGTCTAGTTCA[A/G]CAGTGTCAGAATAGC | 71956 |
rs260639540 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193396 | AGAACTGCGGTTGAT[C/T]TTCAATACCCGCATG | 71956 |
rs260858860 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185195 | AAACTTCATTAGTGG[A/G]TGCTGGGGAAGTTAC | 71956 |
rs261003795 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193514 | AGGCAGAGGCAGATG[A/G]ATCTCTTGAGTTTGA | 71956 |
rs261105895 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193423 | CATGGTGGCTCACAA[C/G]CACCTCTAACTCCAA | 71956 |
rs261113544 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184933 | ATAACACCTGATTCC[G/T]GTCCCTCCAGCCTCT | 71956 |
rs261301748 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196385 | GCCAGCGCTGTTTGG[A/G]AAGAATACAGGTAGA | 71956 |
rs261344853 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80191557 | TGAAAAGAAAAGTTT[A/G]TTTTAGGCCAGCACA | 71956 |
rs261433289 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80192256 | TTTGACTAAAGGAAC[A/T]GGGAGATCTAGCTGG | 71956 |
rs261466691 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80182924 | TGGATGGTTGTGAGC[C/T]ACCCTGTGGTTGCTG | 71956 |
rs261506441 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80191695 | CTCCCATTGGCCTGA[C/T]GACCTTGCTCCACTT | 71956 |
rs261604869 | snp | A/C | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183804 | GAATTAGCAGCTGGG[A/C]GGGTCGAGCTGATGG | 71956 |
rs261775096 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80195782 | ACATCAGTATCAGTC[C/T]GCCACATGCACCTTT | 71956 |
rs261871928 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80194549 | TCCCAATGAAATGAA[A/G]ATCAGTGAAGACGCA | 71956 |
rs261909008 | in-del | -/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80184597 | TTGCCATTTTCCCCC[-/T]TTAACTCAATTGGCC | 71956 |
rs261932449 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190949 | AGTTCAATCCTGAAG[A/G]AACCACCCTGCTCAC | 71956 |
rs262047547 | snp | G/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80198134 | AACTTCTTGCTGGGA[G/T]GTCAAGAAAGAAAAT | 71956 |
rs262078083 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190357 | GTTGAGAGGGTGTGT[A/G]TGCAGGGTAGGGTGT | 71956 |
rs262195380 | snp | A/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80189557 | TTTTTTTTTTTTTTT[A/T]AAAAAAGAGGGACGA | 71956 |
rs262416185 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186830 | CATGCTGGGTCCCAA[A/G]TCCATCGGGAAGGAA | 71956 |
rs262727116 | snp | A/C | | | intron-variant | Rnf135 | Mm_Celera | 11:80186066 | ATATCACTTTCCAAT[A/C]AATGTATCTAGCTAT | 71956 |
rs263163636 | snp | C/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183503 | CACCAGCCCCTGAGG[C/T]TGTCTTTTAATGTCA | 71956 |
rs263201438 | in-del | -/GTAT | | | intron-variant | Rnf135 | Mm_Celera | 11:80197659 | TGTTTGCTCCCCCTG[-/GTAT]ATATATACTGTGTTA | 71956 |
rs263294590 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80196745 | TGGTTAGTGGGCTAG[A/G]AGGGAGGTTGAAGCT | 71956 |
rs263351723 | snp | G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186245 | TGGGTTCAAGTCCCA[G/T]CACCCACATGACACC | 71956 |
rs263753816 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80194555 | TGAAATGAAGATCAG[C/T]GAAGACGCAAGACCA | 71956 |
rs263814824 | snp | A/C | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185582 | GCCTCCCCTCAAGTC[A/C]TGGGATGAGCTGGCC | 71956 |
rs263968604 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80193720 | GGAGGCAGAGGCATG[C/T]GGATTTCTGAGTTTG | 71956 |
rs264031840 | snp | C/G | | | downstream-variant-500B | Rnf135 | Mm_Celera | 11:80200147 | TCCTAGGTTGGCCTC[C/G]AACTCAGAAATCTGC | 71956 |
rs264108225 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80190564 | AACGTGAACTCCTCC[C/T]AGCCTCCTGACTACT | 71956 |
rs264441198 | snp | A/G | | | utr-variant-3-prime | Rnf135 | Mm_Celera | 11:80199291 | CTTGGACTATATGAT[A/G]TGACTGCCCAATTTT | 71956 |
rs264467709 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80197625 | CATATCCATGCTGGC[A/G]TCATCAGTTACAGCT | 71956 |
rs264668870 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192427 | CCATGTGTGATCTGA[A/G]CTGTGGCAGTGTCTG | 71956 |
rs264677420 | snp | G/T | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183050 | TTTTTTTTTTTTTTT[G/T]GTTTTGTTTTGTTTT | 71956 |
rs264929924 | snp | A/G | | | missense | Rnf135 | Mm_Celera | 11:80198995 | GAGAGGCTCCTGTAT[A/G]AGTGTGAGGTCTCTA | 71956 |
rs264939161 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80190691 | CGAGCTGCCTTTGAA[C/T]TCCTGACCCTCCTTT | 71956 |
rs264946503 | in-del | -/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80192156 | GGAACCGAGATTTGT[-/G]GGTATCGTCTGCTCT | 71956 |
rs264990934 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80190111 | GTGCACCGTGTGCAT[A/G]CCTGATATAGAGCGT | 71956 |
rs265232881 | snp | A/G | | | missense | Rnf135 | Mm_Celera | 11:80193976 | CAGGAGATTCTCCAT[A/G]ACCTGGAAGAAATTC | 71956 |
rs265247509 | snp | C/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80185573 | CGAAGCTGTGCCTCC[C/G]CTCAAGTCCTGGGAT | 71956 |
rs265402485 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80188047 | ATAAATTCATTTTTT[A/T]AATTTTTTTAATAGC | 71956 |
rs265582259 | snp | A/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80197802 | TATCTTGCCAATGAC[A/T]ATAATAACATGGTAA | 71956 |
rs265629821 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80181990 | AATGACAGAGCCTCA[C/T]GTGGTCCAGGAGGCA | 71956 |
rs265728486 | snp | A/G | | | utr-variant-5-prime | Rnf135 | Mm_Celera | 11:80183890 | ACAAGGCGGAACCTA[A/G]GGGTGCTTCCTGGCT | 71956 |
rs265821602 | snp | C/T | | | intron-variant | Rnf135 | Mm_Celera | 11:80189020 | GAAAGGGCCCCTTGC[C/T]CCTTTGAGGAGTATT | 71956 |
rs265881303 | snp | A/G | | | intron-variant | Rnf135 | Mm_Celera | 11:80193218 | CACTCAGGAGGCAGA[A/G]GCAGGTGGATCTCTG | 71956 |
rs265929234 | in-del | -/TT | | | upstream-variant-2KB | Rnf135 | Mm_Celera | 11:80183035 | TTTTTTCTTTTTCCA[-/TT]TTTTTTTTTTTTTGG | 71956 |
rs578545705 | snp | A/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183374 | GTCTTCAGACACACC[A/T]GAAGAGGGCATCAGA | 71956 |
rs578646830 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80193787 | CCAGGGCTACACAGA[A/G]AAACCCTGTCTCGAA | 71956 |
rs579221315 | snp | A/G | | | downstream-variant-500B | Rnf135 | GRCm38.p3 | 11:80200049 | AAAAAAGAAAAAAGA[A/G]AAAAAAAAGTCCCTT | 71956 |
rs579237162 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183441 | CTGGGATTTGAACTT[C/T]AGACCTTCGGAAGAG | 71956 |
rs579302896 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80192066 | ACAGAGAAACCTTGT[C/T]TCAAGGGGAAAAAAA | 71956 |
rs579628179 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186613 | AGCGGCAGAGGCAGG[C/T]AGATTTCTGAGTTTG | 71956 |
rs579864222 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182083 | TTTCCTTTCCTTTCC[C/T]TTCCCTTCCCTTCCC | 71956 |
rs579979518 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80184602 | CATTTTCCCCCTTAA[C/T]TCAATTGGCCTATTT | 71956 |
rs580212300 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80181844 | TTAGGTGCTTCTTTG[C/T]TTCTTCTTTCAGTGG | 71956 |
rs580284345 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80196405 | ATACAGGTAGAACCG[C/T]ACAGACAGTGAAAGG | 71956 |
rs580310302 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186823 | ATTCCTGCATGCTGG[A/G]TCCCAAGTCCATCGG | 71956 |
rs580338742 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186632 | TTTCTGAGTTTGAGG[C/T]CAGCCTGGTCTACAG | 71956 |
rs580529941 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182178 | TTTCCTTTCCTTTCC[C/T]TTCCTTTCCTCCTTT | 71956 |
rs580654843 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80197643 | ATCAGTTACAGCTGC[C/T]TGTTTGCTCCCCCTG | 71956 |
rs580915258 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80197290 | TCTCTCTCTCTCCAC[A/G]CATGATATGGTTTCT | 71956 |
rs581316447 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182253 | TTTCTTTCTTTCTTT[C/T]TTTTCTTTCTTTCTT | 71956 |
rs581487921 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80192087 | GGGAAAAAAAAAAGA[C/T]GCTCCTGGCAAACCC | 71956 |
rs581837583 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80193792 | GCTACACAGAAAAAC[C/T]CTGTCTCGAAAAACC | 71956 |
rs581866401 | snp | C/G | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183380 | AGACACACCTGAAGA[C/G]GGCATCAGATCTCAT | 71956 |
rs582153411 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185407 | TATTTTTTAGGGGAC[C/T]TCTCATTATACATGT | 71956 |
rs582413293 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183449 | TGAACTTCAGACCTT[C/T]GGAAGAGCAGTTGGG | 71956 |
rs582451823 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80181849 | TGCTTCTTTGTTTCT[C/T]CTTTCAGTGGAATGA | 71956 |
rs582517917 | snp | G/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80181840 | CTTGTTAGGTGCTTC[G/T]TTGTTTCTTCTTTCA | 71956 |
rs582531604 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80193076 | AAATAAAAAGGATCT[C/T]ATAGACTGGACTATA | 71956 |
rs582948439 | snp | A/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80197437 | TTCTATCCTTGGATC[A/T]TCTTCTTCTTCTTCT | 71956 |
rs583028296 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186614 | GCGGCAGAGGCAGGC[A/G]GATTTCTGAGTTTGA | 71956 |
rs583202854 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182088 | TTTCCTTTCCCTTCC[C/T]TTCCCTTCCCTTCCC | 71956 |
rs583515118 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186648 | CAGCCTGGTCTACAG[A/G]GTAAGTTCCAGGACA | 71956 |
rs583581458 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80189428 | TAAGAGTACTGACTG[C/T]TCTTCCAGAGGTCCT | 71956 |
rs583919331 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80195822 | TGCATGCACACACAC[A/G]CACAAGCAAAAATAT | 71956 |
rs584376476 | snp | A/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183371 | GCTGTCTTCAGACAC[A/T]CCTGAAGAGGGCATC | 71956 |
rs584943178 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80192088 | GGAAAAAAAAAAGAC[A/G]CTCCTGGCAAACCCT | 71956 |
rs584972091 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183440 | GCTGGGATTTGAACT[C/T]CAGACCTTCGGAAGA | 71956 |
rs585330575 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80194649 | TCCTAAACATCACGT[A/G]TCTTCTCGTGGGTCT | 71956 |
rs585500624 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182078 | TTTCCTTTCCTTTCC[C/T]TTCCCTTCCCTTCCC | 71956 |
rs585772789 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80185835 | GTGTGTGTGTGTGAG[C/T]TGTAGCTCCTTTATC | 71956 |
rs585884256 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80193335 | CAAACAAACAAACAA[A/G]CAAGCAAACAATGAA | 71956 |
rs585990505 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80184468 | ATCACAAACAGTTAA[A/G]AATCCAAGTCCCATC | 71956 |
rs586071920 | snp | A/G | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183073 | TTTGTTTTGTTTTTC[A/G]AGACAGGGTTTCTCT | 71956 |
rs586324509 | snp | G/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80181843 | GTTAGGTGCTTCTTT[G/T]TTTCTTCTTTCAGTG | 71956 |
rs586426107 | snp | G/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80196404 | AATACAGGTAGAACC[G/T]TACAGACAGTGAAAG | 71956 |
rs586501238 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80197518 | TTCTTCTTCTTCTTC[A/G]TCCCTTTACATGGAG | 71956 |
rs586538324 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182148 | CTTCCCTTCCCTTCC[C/T]TTCCTTTCCTTTCCT | 71956 |
rs586614263 | snp | A/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80197216 | GCTGTGCCTAACGTG[A/T]TCTCTCTCTCTCTCT | 71956 |
rs587120366 | snp | G/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80183041 | CTTTTTCCATTTTTT[G/T]TTTTTTTTGGTTTTG | 71956 |
rs587182805 | snp | C/T | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186627 | GCAGATTTCTGAGTT[C/T]GAGGTCAGCCTGGTC | 71956 |
rs587235802 | snp | A/G | | | intron-variant | Rnf135 | GRCm38.p3 | 11:80186651 | CCTGGTCTACAGAGT[A/G]AGTTCCAGGACAGCC | 71956 |
rs587440754 | snp | C/T | | | upstream-variant-2KB | Rnf135 | GRCm38.p3 | 11:80182214 | TCTTTTTCTTTTTCT[C/T]TTTCTTTTTTCTTTC | 71956 |