| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs259613316 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108760973 | CAAACAAATCAAATC[A/G]AATACCATTATAGAT | 671564 |
| rs259625904 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743945 | TGACTACAGCTTGTG[G/T]TTCATGTCTGACATG | 671564 |
| rs259716725 | in-del | -/TTT | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776823 | CCTTTTGTAAGATCC[-/TTT]TTTTTTTTTTTTTCA | 671564 |
| rs259724293 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751138 | TAGATATTTTCTTCA[C/T]TTACATTTCAAATGC | 671564 |
| rs259757260 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762606 | ATCTCCTGGGAGAAG[C/T]GGCACCATAAGACTG | 671564 |
| rs259874631 | snp | A/C | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763419 | CCATAGGGAAGGGCA[A/C]TATTAGGAGGTGTGG | 671564 |
| rs260008268 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108761455 | TAAGATTTATTATTA[C/T]ATATTAACTATGAAA | 671564 |
| rs260008316 | snp | C/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775791 | AAAATTCCTGGGCTA[C/T]TTACTTGTATGGAGA | 671564 |
| rs260093601 | snp | A/G | | | synonymous-codon | Rnf212 | Mm_Celera | 5:108774890 | TTTGAGGAGGCAGGA[A/G]TGGCAGTACACGTGC | 671564 |
| rs260201550 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108735001 | TGGACATAGTATTAC[C/T]TGAGGATCCAGCTAA | 671564 |
| rs260235037 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754890 | CAGACAAGTCTAACA[G/T]GATGATTCTAGCTCT | 671564 |
| rs260310927 | in-del | -/AA | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108730212 | ATACAGATGTTGACC[-/AA]AGTCTTGCTCTATTA | 671564 |
| rs260375176 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737654 | ACCAGTACCCCCAGA[-/T]TTCCCAGGGACTAAA | 671564 |
| rs260384573 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746093 | CACAGGTAATATCAC[C/T]GTCTTTGCTTGACCC | 671564 |
| rs260399211 | in-del | -/CTTTGTGC | | | intron-variant | Rnf212 | Mm_Celera | 5:108746579 | AGAGGTGCAGTTTAT[-/CTTTGTGC]CAATGTCCAAGGACC | 671564 |
| rs260421929 | snp | C/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108742836 | CAAGAAACACAATGT[C/G]CCTAATCAGCAGGCA | 671564 |
| rs260599760 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108745905 | ACAGGGCAGGGCAGG[G/T]CAAAGGATCACCTCT | 671564 |
| rs260712780 | snp | C/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766680 | AATCTGCTTATATAA[C/G]AGACTTGAAGAAACC | 671564 |
| rs260712892 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754901 | AACATGATGATTCTA[A/G]CTCTGCATAGTGGAC | 671564 |
| rs260740509 | in-del | -/ATA | | | intron-variant | Rnf212 | Mm_Celera | 5:108770180 | GCTAAGAAGGAAAGT[-/ATA]ATGAGGGTTTAAAAG | 671564 |
| rs260805894 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776851 | TCAATATTAAAGGCA[G/T]ATTTATTGGGAAGCT | 671564 |
| rs260880835 | snp | A/G | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728327 | ATAAATGAAGTAAAC[A/G]AATGTAAATATTTTT | 671564 |
| rs260901478 | snp | A/C | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108764848 | ACCCACCCCCACTCC[A/C]CTACCCACCCACTCC | 671564 |
| rs260919531 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108749138 | GTGATTTGGTGATTT[G/T]GAAGGAGAACCACAT | 671564 |
| rs260979598 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739190 | TCACAACTGAAAGAA[A/T]AAGTATTGGCTCAGG | 671564 |
| rs261074799 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752583 | GTCAATTCTTGATCT[A/T]AGAGCATAAGCCATT | 671564 |
| rs261087104 | snp | A/G | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727702 | GTCCACCTGCCCTGT[A/G]GGCTATGGTTGGTTC | 671564 |
| rs261105494 | in-del | -/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108746150 | TAAAATGTTTATCTG[-/C]CCCCTTTTCAGATGT | 671564 |
| rs261146181 | in-del | -/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108758011 | TAGCGTCTGTATCTT[-/C]CCCTACATTCTGTTG | 671564 |
| rs261172141 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108744596 | GCTGGCCGGCTAGTG[A/C]GCTCTAGGGATCCCT | 671564 |
| rs261302073 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108761000 | GATATTATGAACTGG[-/T]TTTGTGATAAGTACA | 671564 |
| rs261313411 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108750152 | GTGACTTGGACTTCT[A/G]TTCTAAAGTCATATC | 671564 |
| rs261413811 | in-del | -/AA | | | intron-variant | Rnf212 | Mm_Celera | 5:108773304 | ATGAACATGGATCTA[-/AA]ACATGAGCTAAGTTA | 671564 |
| rs261420845 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756485 | ACAGAACCTGGGGAC[C/T]CTACCTGCCTGTCCC | 671564 |
| rs261559657 | in-del | -/GAGA | | | intron-variant | Rnf212 | Mm_Celera | 5:108772985 | TGTGTGTGTGTGTGT[-/GAGA]GAGAGAGAGAGAGAG | 671564 |
| rs261633447 | snp | C/G | | | utr-variant-3-prime | Rnf212 | Mm_Celera | 5:108728826 | TTCTTAGTTCCTGTG[C/G]TGTTGAACTCTGAGA | 671564 |
| rs261808615 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763985 | CAAACCTCTAAAACT[A/G]TAAGCCAGCCCAATC | 671564 |
| rs261860109 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746633 | CAAGGCATGGATGCT[C/T]CATTCCCTGTTAAAC | 671564 |
| rs261873149 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108754254 | GAGCAAGAGTGAAAC[A/C]AATATAGAAATAAAT | 671564 |
| rs261990043 | snp | C/T | | | nc-transcript-variant, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763859 | AGGTTTGGGAGGTCC[C/T]GATGCCAACACTCCT | 671564 |
| rs262044966 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108734814 | AGGGAAATGCAAATC[A/G]AAACAACCCTGAGAT | 671564 |
| rs262048720 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108754093 | TGGCTGTATTCTAGC[C/T]ATGTTCTAAGAACTT | 671564 |
| rs262066519 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752428 | TGGAGTCTAACTTCT[C/T]GAGTTCTTTGTATAC | 671564 |
| rs262157987 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108759930 | CTGCAAGAGACTGGC[C/T]CCTAGAATACTTACA | 671564 |
| rs262316517 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108772853 | CTTTGGTAAAGACAT[C/T]TGCTACTAAGTATGA | 671564 |
| rs262351153 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108751251 | GGCATATAAAGTTTG[C/T]AAGACCAAGGGGCCT | 671564 |
| rs262369457 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108761154 | ATTTGAACTGCGAGT[G/T]GGGTGCTGCCTCAAG | 671564 |
| rs262426243 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733565 | CTTTTCTCATCAACA[C/T]ACACCACTCACAACT | 671564 |
| rs262432705 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732828 | AGGACAGCCTGACAG[C/T]TTCTTACAAAGCTAA | 671564 |
| rs262503704 | snp | G/T | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108768998 | AGAAATTGGTAAAAA[G/T]AATGAGTGTAAGGCA | 671564 |
| rs262569459 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108757287 | GACAGTCACAGATTC[C/T]CTGGGTTTACTGGTG | 671564 |
| rs262619488 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108730225 | CCAAAGTCTTGCTCT[A/G]TTATTGCAGCACGCT | 671564 |
| rs262680341 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108770477 | TTTTAGATACTAGTT[A/T]CTAAGAGTTGAATCC | 671564 |
| rs262692795 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108731747 | CGCTGCCTGTGGAGG[G/T]GATAAAGCACACTGT | 671564 |
| rs262766946 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108741299 | CCCTTGGGCATATAC[C/T]CAAATGACACTCTGT | 671564 |
| rs262800635 | in-del | -/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108749105 | ACATGCAATGAACTA[-/C]CCAGGCACTTAGTAG | 671564 |
| rs262925090 | snp | C/T | | | utr-variant-3-prime, downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728229 | AAATGTGTATAACTC[C/T]ACCTCTAAGGGACCC | 671564 |
| rs262957310 | snp | G/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108767958 | TTTTGAGTTAAAATA[G/T]AAATAAAGAAAGTCC | 671564 |
| rs262958723 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739795 | ATATCAGAAGATGGA[A/G]TGATCTCCCATGCTC | 671564 |
| rs263059783 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729093 | ACCCTGAAGTATTGG[C/T]TCTCTATGGGGGATG | 671564 |
| rs263153557 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108739421 | GAAACCCAATGTTTG[G/T]ATGAGGTGTTTAATT | 671564 |
| rs263218972 | snp | A/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763004 | ATTTTAAACAAAAAA[A/T]GAGCAAAGAAGATTC | 671564 |
| rs263224031 | snp | A/G | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775936 | TTTCATCAGGCCCTT[A/G]AAAAATTAGAGGTCC | 671564 |
| rs263240035 | in-del | -/AA | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108763231 | ATTCATAGCTCGTGT[-/AA]AAAAAAAAAAAAGAC | 671564 |
| rs263257235 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737670 | TTCCCAGGGACTAAA[C/T]CACCAACCAAAGGGT | 671564 |
| rs263280126 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762641 | GCTGCCTTATGAGAT[A/G]GGGCTACCACAGTTT | 671564 |
| rs263319537 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108737245 | CTAAGATACAATTCA[C/T]AGACCACATGAAGCT | 671564 |
| rs263445517 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744159 | TCCTAGACACTGAAG[C/T]TGTAATAGCAGCCAC | 671564 |
| rs263460510 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738152 | AGCTGTCCCCTGAGA[A/G]GCTCTGCCAGAGCCT | 671564 |
| rs263525258 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108770286 | TTAGGGACATCTTGG[A/G]TAACACAATAATAAA | 671564 |
| rs263672664 | in-del | -/T | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775269 | TGTTGCTAAGGAAGC[-/T]TGGGTGAAGCTGGGT | 671564 |
| rs263675810 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108747948 | TTGGTTTTCCTGGAC[A/T]GAGATGTTACTTCAA | 671564 |
| rs263731222 | snp | A/C | | | intron-variant | Rnf212 | Mm_Celera | 5:108741947 | GAGACACCAACCTGG[A/C]CACAAAACATTTGAC | 671564 |
| rs263888705 | snp | A/G | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769282 | AAAGAGCATACACAG[A/G]TTGGACCTAGGCTTC | 671564 |
| rs263936258 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108741530 | AGTAACCCAGGCCCA[A/G]AAGTATAAACATAAT | 671564 |
| rs263939149 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740499 | AAGATCCAGACTTAA[A/G]TCCACACTCCTATGA | 671564 |
| rs264277133 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729507 | AGAGATGTAAAGAGA[-/T]TGTGAGCTTTGACAT | 671564 |
| rs264280024 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744975 | TCAATTACCAGTAAA[G/T]AAAGAGACAAGACAA | 671564 |
| rs264287201 | in-del | -/AT | | | intron-variant | Rnf212 | Mm_Celera | 5:108743393 | GGAATCAGCCTGGAC[-/AT]ATGTTTTTATGCTGT | 671564 |
| rs264293115 | in-del | -/GT | | | downstream-variant-500B | Rnf212 | GRCm38.p3 | 5:108727916 | TACTAGCTGGGTATA[-/GT]GTGGCCCATGCCTTT | 671564 |
| rs264307979 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108739961 | TAGGGAGAAAACTCT[A/G]GGCTAACACATCTTC | 671564 |
| rs264365399 | in-del | -/AAAT | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776799 | GCTCCACAAGGGTTG[-/AAAT]AAATTGTTACCTTTT | 671564 |
| rs264404797 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744715 | CTACAGCAAGCACTT[G/T]ATTCACTGAGATTTC | 671564 |
| rs264416716 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108753691 | AGGTACTACTACCCC[C/T]ATGCTTTCCTACTGT | 671564 |
| rs264431677 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752813 | AGAGTACTGGATTTC[C/T]CAGAACTGGAGTTAC | 671564 |
| rs264569094 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108743475 | TTGCCTACTTTAGAT[C/T]TTCATAATTAATATA | 671564 |
| rs264746101 | snp | C/T | | | missense | Rnf212 | Mm_Celera | 5:108747444 | GAGTCAGGTCAATGT[C/T]CATTGACTCTATTCT | 671564 |
| rs264904846 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108754717 | ATGAGGGGCTACTGT[A/G]TGAAGATGTGAAGCT | 671564 |
| rs264986019 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108752767 | GCATTCTTCTACATA[G/T]TGCCTTTCAGATGCC | 671564 |
| rs265062483 | snp | C/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108762517 | GATTTTAAAAATACA[C/G]TTAGCAAACTAGTAT | 671564 |
| rs265170333 | snp | G/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108732926 | CATGCTTACACAATA[G/T]CTATAGTAGACAATA | 671564 |
| rs265201875 | snp | A/C | | | downstream-variant-500B, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108769313 | CTCCCCTAACACACA[A/C]ATATGTAGCAGATGT | 671564 |
| rs265232554 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108757951 | AGCACAGACAAAAGG[A/G]CGGTCTTCATTCACC | 671564 |
| rs265386958 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108756019 | ATCAGGACCTTTGTA[C/T]AGAGCTGAGTCATGT | 671564 |
| rs265397124 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108766883 | GTGTATGCTCAAAAA[A/G]GAATTTTGGTGGTTG | 671564 |
| rs265420550 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108740099 | CCTAAGACCTATAAA[A/G]TCCCCTTGCATTAGC | 671564 |
| rs265515610 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730552 | TTTCAAATTCACACA[-/T]TACCAACTTTTCTCT | 671564 |
| rs265539997 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108763675 | GTTTATTGAGGAGGT[A/G]GGGAGAGGGTGGTGG | 671564 |
| rs265590543 | in-del | -/TAT | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108765925 | TGCCACTGTTACTAC[-/TAT]ATCACTGCATAGGTT | 671564 |
| rs265697839 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108774548 | ACCTGTCCCTTTACT[C/T]GCCAAATTAAATAGG | 671564 |
| rs265804876 | in-del | -/ATT | | | intron-variant | Rnf212 | Mm_Celera | 5:108743922 | CATTATATGGGAAAC[-/ATT]AATACTGACTACAGC | 671564 |
| rs265895429 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108740739 | TAGCCTTGAATGCAC[C/T]GACACAGGAAACAAC | 671564 |
| rs265920977 | in-del | -/TCAGCTGCCTCAAGCTATTGT | | | intron-variant | Rnf212 | Mm_Celera | 5:108755470 | GTAGATATGATATGA[-/TCAGCTGCCTCAAGCTATTGT]TGTCATGCCTCTCCG | 671564 |
| rs265965376 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108746672 | ACTCTGGAATCTATA[C/T]TCCATCATAAGCAGG | 671564 |
| rs266055587 | snp | A/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108745116 | AACTCTCAGCCAACC[A/G]GTTGTTGTGGATTGC | 671564 |
| rs266130794 | snp | A/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108753999 | AAAGAACACTGACAG[A/T]AATGTAGATAGTGGA | 671564 |
| rs266203572 | snp | C/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108744024 | TTGTGCCCCCTAGTG[C/T]CTAGTGGTATCAGTG | 671564 |
| rs266216826 | snp | C/T | | | intron-variant, utr-variant-5-prime | Rnf212 | Mm_Celera | 5:108750954 | GAAGAAGGATGAAAG[C/T]ACTTACACTTTGGTC | 671564 |
| rs386836536 | in-del | -/CAAAAA | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108728070 | AAACAAAAACAAAAA[-/CAAAAA]TAAAATAAAAAACCA | 671564 |
| rs386882774 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751856 | TGATACCCTCCAGAT[C/G]CATCCATTTGCCTAA | 671564 |
| rs386884977 | in-del | -/A | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775406 | CCACAAAAATCAAGA[-/A]GAACCATAGGTTCCT | 671564 |
| rs386914823 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108730553 | TTCAAATTCACACAT[-/T]ACCAACTTTTCTCTT | 671564 |
| rs386989710 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108737800 | GTCCCAGTGTAGGGG[-/G]AATGCCAGGATAGGG | 671564 |
| rs387061994 | in-del | -/GACAT | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108742176 | AATGAATGAATGAAT[-/GACAT]AATTCCTAATGATAT | 671564 |
| rs387107824 | in-del | -/TA | | | intron-variant | Rnf212 | Mm_Celera | 5:108747521 | ATAAACATCAGTTTA[-/TA]AACATCCCTGCATGT | 671564 |
| rs387235700 | in-del | -/T | | | intron-variant | 1700047L14Rik, Rnf212 | Mm_Celera | 5:108765973 | CCTTTTTTTTTTTTT[-/T]CCAAGTCTTGATATG | 671564 |
| rs387236219 | in-del | -/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108733838 | GAGAGCAAAGAATCA[-/T]TTTTTTTTAGAGTTT | 671564 |
| rs387258523 | in-del | -/C | | | upstream-variant-2KB | Rnf212 | Mm_Celera | 5:108775616 | GGTCATTCTCCCCCC[-/C]ACCCCCCATTTAAAA | 671564 |
| rs387284308 | in-del | -/TT | | | intron-variant | Rnf212 | Mm_Celera | 5:108733845 | AAGAATCATTTTTTT[-/TT]AGAGTTTAATTACTT | 671564 |
| rs387311491 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108729508 | GAGATGTAAAGAGAT[-/T]GTGAGCTTTGACATG | 671564 |
| rs387381804 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108738108 | TATTGATGATGCCAA[-/A]GAAGCACTTGCAGAT | 671564 |
| rs387456003 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108739110 | CTAAAAAAAAAAAAA[-/A]TCAGTAGATCTCCTG | 671564 |
| rs387493272 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108741081 | CATCCTTAGCCATCA[A/G]GAAATGAAAATCAAA | 671564 |
| rs387519143 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108759481 | TTGAGACTGCAGAAA[-/A]GGCCAACACCGAGGA | 671564 |
| rs387519871 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108743225 | CACCCAAGCCAGAGG[-/G]AAGCATATTCCCTGG | 671564 |
| rs387542930 | in-del | -/ACACACACACACACACACACACACAC | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108761262 | CATTACAACAAACTT[-/ACACACACACACACACACACACACAC]ACACACACACACACA | 671564 |
| rs387546057 | in-del | -/TG | | | downstream-variant-500B | Rnf212 | Mm_Celera | 5:108727919 | TAGCTGGGTATAGTG[-/TG]GCCCATGCCTTTAAT | 671564 |
| rs387568560 | in-del | -/GA | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | Mm_Celera | 5:108776996 | ATAGAGAGAGAGAGA[-/GA]TAAAGAATATATGTA | 671564 |
| rs387613945 | in-del | -/AA | | | intron-variant | Rnf212 | Mm_Celera | 5:108729590 | AAGTTGAAAAAAAAA[-/AA]GAGTTCACTGATTTA | 671564 |
| rs387630021 | in-del | -/TTTTCCGA | | | intron-variant | Rnf212 | Mm_Celera | 5:108774512 | CGCAGTCTACAAGAA[-/TTTTCCGA]GGGCTGGTGGTGTAC | 671564 |
| rs387633268 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108738469 | TGGGAGTGTGGGGGG[-/G]AAGACCCTCATAGAA | 671564 |
| rs387717353 | in-del | -/G | | | intron-variant | Rnf212 | Mm_Celera | 5:108737798 | ATGTCCCAGTGTAGG[-/G]GGAATGCCAGGATAG | 671564 |
| rs387782495 | in-del | -/T | | | intron-variant | Rnf212 | Mm_Celera | 5:108733968 | CTATTGTGATTTTTT[-/T]AATTAGGTATTTTCT | 671564 |
| rs387796490 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108760790 | GGGAGAAAAAAAAAA[-/A]CAGTGGGTGTGGTGA | 671564 |
| rs387854453 | in-del | -/TTTGTGCC | | | intron-variant | Rnf212 | Mm_Celera | 5:108746580 | GAGGTGCAGTTTATC[-/TTTGTGCC]AATGTCCAAGGACCT | 671564 |
| rs387866632 | in-del | -/A | | | intron-variant | Rnf212 | Mm_Celera | 5:108740922 | CCTGACAGAGGGCTA[-/A]TATCCAAAAGAAATA | 671564 |
| rs578444466 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734417 | GTGTCAGCGTTTGGA[A/G]GCTGATTATGGATGG | 671564 |
| rs578488869 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748292 | AATATTCTCAATACA[G/T]ATATCTACTCTACAT | 671564 |
| rs578602924 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108773809 | CTGATTCACCATTAA[C/T]ATTCCTGACTCTTTT | 671564 |
| rs578664431 | snp | A/G | | | downstream-variant-500B | Rnf212 | GRCm38.p3 | 5:108728027 | ATAGCCAGGGCTATG[A/G]GAGAGACTCCGTCTA | 671564 |
| rs578688776 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751923 | GTACTCCATTGTGTA[A/C]ATGTACCACATTTTC | 671564 |
| rs578771041 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108749037 | GAAGATCTAAGTCCT[A/G]ACTCTGGGACCCAAG | 671564 |
| rs578860220 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108758001 | ATAGCTGCATTAGCG[C/T]CTGTATCTTCCCCTA | 671564 |
| rs579023239 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108774589 | CCCACTGCTTTGTAC[A/G]CATGCGGCCCCCGGC | 671564 |
| rs579073886 | snp | C/G | | | utr-variant-3-prime | Rnf212 | GRCm38.p3 | 5:108728800 | GAAGTAGAGTGAGCA[C/G]CACAACCCCCTTCTT | 671564 |
| rs579075618 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752059 | TGGAACATCTTCTGG[A/G]TATATGCCCAGGAGA | 671564 |
| rs579180285 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108754683 | TGTGTAGTACAGTTG[A/G]ATTCTATGCAAGGAG | 671564 |
| rs579234906 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734252 | TCAGCTCCTTGGGTA[C/T]TTTCTCTAGTTCCTC | 671564 |
| rs579357124 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108738601 | GAAGGCAAGATTACC[C/T]GCCCTCCCCCCCCCA | 671564 |
| rs579378932 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752114 | ACTATGTCCAATTTT[C/T]TGAGGAACTGTCAGA | 671564 |
| rs579384081 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108730547 | TCCCTTTTTCAAATT[C/T]ACACATACCAACTTT | 671564 |
| rs579547865 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108737578 | CCAATGGAGGAGCTA[A/G]AGAAAGGACACAAGG | 671564 |
| rs579554512 | snp | A/C | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108764944 | CTTTCCAGTGATGGC[A/C]AACTAGGCCATCTTT | 671564 |
| rs579620577 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751370 | GTTGTTCTACCTATA[G/T]GGTTGCAGACCCCTT | 671564 |
| rs579674052 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108743521 | TAACATTAGAAGGAC[A/G]AGACAGCAGTGGAAC | 671564 |
| rs579829635 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108732806 | GTTGGAGAAGACAAG[C/T]CTCGGAAGGACAGCC | 671564 |
| rs579969872 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734441 | TGGATGGATCCCTGG[A/G]TATGGCAGTCTCTAC | 671564 |
| rs580053778 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751497 | TGGCCTAGCCTCACA[A/C/T]GAGACAGCTATATCA | 671564 |
| rs580078595 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108762257 | GTATCTTTATTCCTG[A/G]AATCTTATGTGGGTT | 671564 |
| rs580176943 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734005 | ACATTTCCAATGCTA[C/T]CTCAAAAGTCCCCCA | 671564 |
| rs580177867 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108740176 | GGCTCAGAAGCTGCA[C/T]CTAATAAACACACCT | 671564 |
| rs580180780 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752255 | GCCATTCTGACTGGT[G/T]TGAGGTAGAATCTCA | 671564 |
| rs580246566 | snp | A/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108735111 | TTTATAATAGCCAGA[A/T]GCTGGAAAGAACCCA | 671564 |
| rs580293295 | snp | C/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108763228 | CATCATTCATAGCTC[C/G]TGTAAAAAAAAAAAA | 671564 |
| rs580497726 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752338 | AGGTGCTTCTCAGCC[A/T]TTCGGTATTCTTCAG | 671564 |
| rs580541923 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734054 | CCCTACCCACCCACT[C/T]CCACTTCTTGGCCCT | 671564 |
| rs580654295 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751853 | GGATGATACCCTCCA[G/T]ATCCATCCATTTGCC | 671564 |
| rs580815537 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108772247 | CTACATAGAAACCTC[A/G]TCTCAAACAAAACAA | 671564 |
| rs580840014 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748429 | CATATATCTACTCTA[C/T]ATAATATTCTCAATA | 671564 |
| rs580966858 | snp | A/T | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108764980 | CATATGCAGCTAAAG[A/T]CAAGAGCTCCGGGGT | 671564 |
| rs580974432 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734112 | AGTTTGCAAGACCAA[G/T]GGGCCTCTCTTCCCA | 671564 |
| rs580981941 | snp | A/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108753890 | AGGGAGAATGTGAAG[A/T]GTCTAGAATTTAGGG | 671564 |
| rs581085698 | snp | A/G | | | downstream-variant-500B | Rnf212 | GRCm38.p3 | 5:108728074 | CAAAAACAAAAATAA[A/G]ATAAAAAACCAACTA | 671564 |
| rs581092147 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751946 | ACATTTTCTGTTATC[C/T]ATTCCTCTGTTGAGG | 671564 |
| rs581138459 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108737979 | AAATGCAGGGACAAA[A/G]AGTCGAGTAGAGACT | 671564 |
| rs581166295 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734175 | ATGCAGCTAGAGATA[C/T]GAGCTCTGGGGGTTA | 671564 |
| rs581291445 | snp | A/C | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108754665 | GTCATTGAGACCAAG[A/C]AATGTGTAGTACAGT | 671564 |
| rs581435177 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108738118 | GCCAAAGAAGCACTT[A/G]CAGATAGGAGCCAGG | 671564 |
| rs581496087 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108767297 | TGTGATGTGTGGAAG[A/G]AAGGCAGAAGGAATC | 671564 |
| rs581625322 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751705 | GAAGTATCCACACTT[A/T]GGTCTTCCTTCTTTT | 671564 |
| rs581731066 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748080 | TCTCAATACAGATAT[C/T]TACTCTACATAATAT | 671564 |
| rs581779673 | snp | A/C | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108732771 | TCTTATTCCTTTGAT[A/C]TCTTTCCTTGTCAGC | 671564 |
| rs581861863 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752123 | AATTTTCTGAGGAAC[C/T]GTCAGACTGATTTCC | 671564 |
| rs581983166 | snp | A/C | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108739097 | GATACAAGATCAACT[A/C]AAAAAAAAAAAAATC | 671564 |
| rs582080379 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108773831 | GACTCTTTTGAATTC[C/T]AGATTTCCCATTCAG | 671564 |
| rs582089670 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734437 | ATTATGGATGGATCC[C/T]TGGATATGGCAGTCT | 671564 |
| rs582095048 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108761592 | TTGCCATTATTCCTG[A/G]AATCTTTTTTTTTCC | 671564 |
| rs582202317 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108739374 | GATAGACAAGGCGCA[C/T]AGGAAAATGGAAGTT | 671564 |
| rs582316833 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734847 | CACCTCATACCAGTC[G/T]GAGTGGCTAAGATCA | 671564 |
| rs582343767 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752218 | TTTCCAGCATCTGCT[A/G]TCATCTGAATTTTTG | 671564 |
| rs582468185 | snp | A/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108762264 | TATTCCTGGAATCTT[A/T]TGTGGGTTTTTAGAT | 671564 |
| rs582553486 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108749639 | CCATGTACATAACTG[A/G]CACTTCTGGTCACAA | 671564 |
| rs582600929 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | Tmed11, Rnf212 | GRCm38.p3 | 5:108776925 | GTCATGGGGATAAGG[G/T]GGCAAGGGGAAGAGA | 671564 |
| rs582764286 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752065 | ATCTTCTGGATATAT[G/T]CCCAGGAGAGGAATT | 671564 |
| rs582800585 | snp | A/C | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734105 | CATATAAAGTTTGCA[A/C]GACCAATGGGCCTCT | 671564 |
| rs582818995 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734312 | CTGACTGTGAGCATC[C/T]ACTTCTGTGTTTGCT | 671564 |
| rs582868062 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751293 | GATGGCCGACTAGGC[C/T]ATCTTCTGATACATA | 671564 |
| rs582912755 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108764977 | ATACATATGCAGCTA[A/G]AGACAAGAGCTCCGG | 671564 |
| rs582958107 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752342 | GCTTCTCAGCCTTTC[A/G]GTATTCTTCAGTTGA | 671564 |
| rs582988054 | snp | A/C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751459 | GCTGACTGTGAGCAT[A/C/T]CACTTCTGTGTTTGC | 671564 |
| rs583248040 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108737806 | GTGTAGGGGGAATGC[C/T]AGGATAGGGAAATAG | 671564 |
| rs583252027 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108764945 | TTTCCAGTGATGGCC[A/G]ACTAGGCCATCTTTT | 671564 |
| rs583450180 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108744659 | GTTGTGCCTGGTTTT[C/T]ATGTGGGTACCTGGG | 671564 |
| rs583562251 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752274 | GGTAGAATCTCAGGG[C/T]TGTTTTGATTTGCAT | 671564 |
| rs583605498 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751597 | ATCCCCGGGTGGGGC[A/C]GTCTCTGGATGGTCC | 671564 |
| rs583738997 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734007 | ATTTCCAATGCTATC[C/T]CAAAAGTCCCCCATA | 671564 |
| rs583823430 | snp | A/G | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108764380 | TTATTTTTATTTTTG[A/G]TACTAAGTACAAATA | 671564 |
| rs584000490 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751709 | TATCCACACTTAGGT[C/G]TTCCTTCTTTTTCAC | 671564 |
| rs584117336 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108735133 | AAGAACCCAGATGTC[A/G]TTCAACAGAAGAATG | 671564 |
| rs584197645 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748261 | AATATTCTCAATACA[G/T]ATATCTACTCTACAT | 671564 |
| rs584206023 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734335 | TGTTTGCTAGGCCCC[A/G]GCATAGCCTCACAAG | 671564 |
| rs584450937 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108739371 | GGAGATAGACAAGGC[A/G]CATAGGAAAATGGAA | 671564 |
| rs584492792 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748457 | ATACAGATATCTACT[C/T]TACATAATATTCTCT | 671564 |
| rs584497874 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108737999 | GAGTAGAGACTGAAG[A/G]AAAGGCCATCCAGAG | 671564 |
| rs584693771 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734124 | CAATGGGCCTCTCTT[C/T]CCAATGATGGCCGAC | 671564 |
| rs584699151 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108753892 | GGAGAATGTGAAGAG[C/T]CTAGAATTTAGGGTT | 671564 |
| rs584703517 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108754673 | GACCAAGCAATGTGT[A/G]GTACAGTTGGATTCT | 671564 |
| rs584802687 | snp | A/G | | | downstream-variant-500B | Rnf212 | GRCm38.p3 | 5:108728078 | AACAAAAATAAAATA[A/G]AAAACCAACTAAGCA | 671564 |
| rs584811134 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752028 | ACATAGTGGAACATG[A/T]GTCTTTATTACAAGT | 671564 |
| rs584983002 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734232 | CTATAGGGTTGCAGA[C/T]CCCTTCAGCTCCTTG | 671564 |
| rs585081488 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751296 | GGCCGACTAGGCCAT[C/G]TTCTGATACATATGC | 671564 |
| rs585158617 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108738335 | GATTAAACCACCAAC[C/T]AAAGAGTACACATGG | 671564 |
| rs585164850 | snp | C/T | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108767701 | TAAAAAAAAATACCC[C/T]AACACCAAAGACGCT | 671564 |
| rs585169907 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752125 | TTTTCTGAGGAACTG[C/T]CAGACTGATTTCCAG | 671564 |
| rs585472898 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108742771 | TTGTGTTGCTGTAGT[G/T]TGACGAGAAGAAGTT | 671564 |
| rs585620396 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108739657 | GCCATTCTTGGTACC[C/T]ATGAGCTGTTGCATG | 671564 |
| rs585623116 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108732794 | TTGTCAGCTGTTGTT[A/G]GAGAAGACAAGCCTC | 671564 |
| rs585718205 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734438 | TTATGGATGGATCCC[C/T]GGATATGGCAGTCTC | 671564 |
| rs585720462 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751486 | TTGCCAGGCACTGGC[A/C]TAGCCTCACATGAGA | 671564 |
| rs585725706 | snp | A/G | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108762124 | CATCCTTTCATCTCA[A/G]CTCCAAACTTTGTCT | 671564 |
| rs585727071 | snp | C/T | | | upstream-variant-2KB, intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108762411 | TTTTTTTCAAAAAGG[C/T]GAATGTATTCTCCAC | 671564 |
| rs585956702 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108773837 | TTTGAATTCCAGATT[C/T]CCCATTCAGGACTAC | 671564 |
| rs585981025 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108732860 | CGTGTTCTTTCTATA[C/T]GACCACCATAACTAG | 671564 |
| rs585984930 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752236 | ATCTGAATTTTTGAT[C/T]TTAGCCATTCTGACT | 671564 |
| rs586062169 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108735008 | AGTATTACTTGAGGA[C/T]CCAGCTAAACCACCC | 671564 |
| rs586280833 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751132 | TTTTATTAGATATTT[C/T]CTTCACTTACATTTC | 671564 |
| rs586293317 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752085 | GGAGAGGAATTGCTG[C/G]ATCTTCCAGTGGTAC | 671564 |
| rs586387596 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108741197 | AAGAGGAACACTCCT[C/T]CATTGCTGCTGGGAG | 671564 |
| rs586660823 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108735158 | AGAATGGATACAGAA[A/G]ATGTAGTACATTTAC | 671564 |
| rs586664821 | snp | C/G | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108764842 | ATACCCACCCACCCC[C/G]ACTCCACTACCCACC | 671564 |
| rs586736436 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108745793 | AGTCCAGTTCTATTT[A/G]TAAGGACTCGTCCTG | 671564 |
| rs586767590 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734106 | ATATAAAGTTTGCAA[G/T]ACCAATGGGCCTCTC | 671564 |
| rs586778276 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752349 | AGCCTTTCGGTATTC[C/T]TCAGTTGAGAATTCT | 671564 |
| rs586877976 | snp | A/T | | | intron-variant | 1700047L14Rik, Rnf212 | GRCm38.p3 | 5:108765868 | AGGCTACTTTTGACC[A/T]CAGCTTTCACAGCAA | 671564 |
| rs587054963 | snp | A/G | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108737968 | CTGTCTAAAGGAAAT[A/G]CAGGGACAAAAAGTC | 671564 |
| rs587090456 | snp | A/C | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734025 | AAAGTCCCCCATACC[A/C]TCCCCCGCCACTCCC | 671564 |
| rs587165341 | snp | A/C | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108734136 | CTTCCCAATGATGGC[A/C]GACTAGGCCATCTTC | 671564 |
| rs587169078 | snp | G/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108754132 | CTGAATTAAAAGGAA[G/T]AGACTAATTTGTTTG | 671564 |
| rs587204686 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751848 | ACTCAGGATGATACC[C/T]TCCAGATCCATCCAT | 671564 |
| rs587221746 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108751640 | CAGTTCCAAACTTTG[C/T]CTCTGTAACTCCTTC | 671564 |
| rs587255634 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108738102 | AGACACTATTGATGA[C/T]GCCAAAGAAGCACTT | 671564 |
| rs587405695 | snp | C/T | | | intron-variant | Rnf212 | GRCm38.p3 | 5:108748023 | ATACAGATATCTACT[C/T]TACATAATATTCTCA | 671564 |
| rs587459151 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf212 | GRCm38.p3 | 5:108752327 | AACATTTTTTCAGGT[A/G]CTTCTCAGCCTTTCG | 671564 |