| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
|---|
| rs3656054 | snp | A/C | 0.5 | 0 | intron-variant | Rnf10 | Mm_Celera | 5:115264973 | TATATGACACATACA[A/C]ACACACACACACACA | 50849 |
| rs4138145 | snp | C/T | 0.5 | 0 | intron-variant | Rnf10 | Mm_Celera | 5:115264969 | TATATATATGACACA[C/T]ACAAACACACACACA | 50849 |
| rs6261339 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261519 | caggagccgggagcc[A/G]gngcattagagtaac | 50849 |
| rs6261341 | snp | A/C | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261521 | ggagccgggagccng[A/C]gcattagagtaacca | 50849 |
| rs6261804 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261586 | TACCTCAATCCACAA[A/G]TAAATAATATATAAA | 50849 |
| rs6261869 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261624 | CTGTCTCAAATAAAG[C/T]TGAAGTctaaagagg | 50849 |
| rs6275520 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261811 | ataaatgcaggcaaa[C/T]acacacataaaataa | 50849 |
| rs6328077 | snp | C/T | 0.5 | 0 | intron-variant | Rnf10 | Mm_Celera | 5:115271215 | ggccagcctggtcta[C/T]agagtgagttncagg | 50849 |
| rs6328094 | snp | C/T | 0.5 | 0 | intron-variant | Rnf10 | Mm_Celera | 5:115271226 | tctanagagtgagtt[C/T]caggacaggcaagga | 50849 |
| rs6328576 | snp | C/T | 0.5 | 0 | intron-variant | Rnf10 | Mm_Celera | 5:115271276 | cgaaaaaccaaaAGA[C/T]TGATTGAAAAAAAAA | 50849 |
| rs6343708 | snp | A/C | 0.5 | 0 | intron-variant | Rnf10 | Mm_Celera | 5:115271774 | CTGAACCTAAATGAA[A/C]TGAATGCAGGGTCTG | 50849 |
| rs13474671 | snp | A/G | | | utr-variant-3-prime | Rnf10 | Mm_Celera | 5:115241880 | AAAGCCCCTCCCCCC[A/G]CCCCAAGCTAATCAA | 50849 |
| rs13474673 | snp | C/T | | | missense | Rnf10 | Mm_Celera | 5:115257004 | AGTGGGGACACAAGC[C/T]TTTCAACAAGGAGCT | 50849 |
| rs13474674 | snp | C/T | | | utr-variant-3-prime | Rnf10 | Mm_Celera | 5:115241899 | GTATTTGAGTTTGAA[C/T]AGATTGATTAGCTTG | 50849 |
| rs13474675 | snp | G/T | | | synonymous-codon | Rnf10 | GRCm38.p3 | 5:115249147 | GGAGTATCTGTCTGC[G/T]TTTGATGATGAAGCT | 50849 |
| rs13474676 | snp | A/G | | | stop-gained | Rnf10 | Mm_Celera | 5:115250111 | GCAGCTCAGCCAGTA[A/G]TCCAAGCTGCTGCTG | 50849 |
| rs13474677 | snp | C/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115251109 | GTTGGTGGCCCTGCC[C/G]AAATCCAAGTGGGTG | 50849 |
| rs13474678 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Rnf10 | Mm_Celera | 5:115249003 | TCTGGGAGAGGGGAC[C/T]GTTGGTCCTGAGATG | 50849 |
| rs13474679 | snp | A/G | | | missense | Rnf10 | Mm_Celera | 5:115242499 | TGATGGGGAGAGTGA[A/G]AATTCTGACCGTGTT | 50849 |
| rs13474680 | snp | A/G | | | missense | Rnf10 | Mm_Celera | 5:115242514 | CGCCCCTGTGGACAG[A/G]GATGGGGAGAGTGAC | 50849 |
| rs13474681 | snp | C/G/T | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115249487 | AGGAGTGGCTGGAGG[C/G/T]GGAGGGGAGGTCACT | 50849 |
| rs29530915 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273133 | GAACTCTTTGTGTGC[A/G]ACAGTCTGGCTTCCA | 50849 |
| rs29566887 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115268820 | CCAAGGCTGTAGACT[A/G]AAAGATCAAGAAACT | 50849 |
| rs29583537 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115250255 | CTGGGCTAGCTCAAA[A/G]ACCTAAGCAGCCAGA | 50849 |
| rs29633811 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf10 | Mm_Celera | 5:115250703 | TGCCTGCCCCAGGAC[C/T]TTAGTCTTTAAGACA | 50849 |
| rs29680275 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273817 | TGAGTGGAATTTTAG[C/T]AATCGTGTATGTAGG | 50849 |
| rs29766342 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115242115 | CACAGTACTGTGGGC[A/G]CCCAGGTGAAATGGC | 50849 |
| rs29779958 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf10 | Mm_Celera | 5:115270859 | GGCACTGGAAAACTA[A/C]GGGGTGTGCTCTTCC | 50849 |
| rs29824774 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Rnf10 | Mm_Celera | 5:115258391 | CCGTCTGTCCGCTGG[C/G]CTGCTCCAGGTCAGC | 50849 |
| rs32137514 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256825 | CCACTCCTGGTCCCA[A/G]AAGTCACGGCAAGCA | 50849 |
| rs32137515 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256920 | CCCCCTGACTGGTTA[G/T]ATGAGGTGTCCTCCT | 50849 |
| rs32137516 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257335 | GCATCCCGACTGTCC[C/T]GTCGCCCTGCTCAGC | 50849 |
| rs32137517 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115257336 | CATCCCGACTGTCCC[A/G]TCGCCCTGCTCAGCA | 50849 |
| rs32137518 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257512 | CAAACCTTTTACCTC[C/T]ATGTCAAATCCACAC | 50849 |
| rs32137519 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258182 | GATGGAGTTAGAGCA[C/T]GAAGGTAAGAACTAG | 50849 |
| rs32137520 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258378 | AACGTCCGTCTGTCC[A/G]TCTGTCCGCTGGGCT | 50849 |
| rs32137521 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258387 | CTGTCCGTCTGTCCG[C/T]TGGGCTGCTCCAGGT | 50849 |
| rs32137522 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258904 | TTTAATGCCATTATT[G/T]ACTTTAATGTGCAAG | 50849 |
| rs32137523 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259689 | ACACACAGCATGGAC[A/T]GTCAAACAACAGCAC | 50849 |
| rs32138394 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260344 | AAATAAAAGTAATAA[A/G]TTTAATGTTTTCCCA | 50849 |
| rs32138395 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260445 | CTGTGAGAAAGCTAA[A/G]CTTAGTCCATAGCAC | 50849 |
| rs32138396 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260766 | CACGCTATGGAAGCT[A/T]CAGAGTTAACACATA | 50849 |
| rs32138397 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260782 | CAGAGTTAACACATA[A/C]ACGCTGAGCTCCAGG | 50849 |
| rs32138398 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261929 | TCTAATTTCACATAA[A/C]AGTACTGAAGATTAT | 50849 |
| rs32138399 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115262259 | TATCTGTTGACCAAA[C/T]ATCTATACTCTGGGT | 50849 |
| rs32138400 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262644 | CAGCATGACTAATGA[A/G]CTTTAACAAGGAACA | 50849 |
| rs32138401 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115263090 | CGGAGGTGTTAGTGG[A/C]GGCTGCAGCTGGTAC | 50849 |
| rs32138402 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263476 | CTTTTGTATGATAGC[C/G]ATCCTGTTTCAACTT | 50849 |
| rs32138403 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263531 | TGTCTGACATGAACC[A/G]TGAATGATCTTGTCA | 50849 |
| rs32138543 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243658 | TCACAGGGTAACCTA[C/T]TCTGGTTGAAGTTCT | 50849 |
| rs32139034 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265670 | TTTTCATGTGTGGAA[A/G]TTTTCGTGTGTATAC | 50849 |
| rs32139214 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243874 | CTCTGTCCTGAGCCA[A/G]TCTCTCAGCACTGTG | 50849 |
| rs32139215 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243899 | ACTGTGCATGTGGTG[A/G]TGATGTGGGTGATGC | 50849 |
| rs32139216 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115244013 | GCTTTCTCAAGCAAA[A/G]GATTTACCTGGGCAA | 50849 |
| rs32139217 | snp | C/G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244175 | TTTAATGAGAAACAA[C/G/T]CATGAGAGCCAGGCA | 50849 |
| rs32139218 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244378 | TTAATCCTGCCCTGT[C/T]CTTATTCCAGAGTAC | 50849 |
| rs32139219 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244391 | GTTCTTATTCCAGAG[C/T]ACTAGGCATTGCCTA | 50849 |
| rs32139220 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244418 | CCTACACCAGTGAAC[A/G]CAGACAAGAGGCTTC | 50849 |
| rs32139221 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244452 | AAGCTCCTTTAACAC[C/T]GGCATGCAACCACAG | 50849 |
| rs32139222 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244590 | AAATAAAAACAGAAA[A/G]GCTTGCTAGCTCTCC | 50849 |
| rs32139223 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244599 | CAGAAAGGCTTGCTA[A/G]CTCTCCAAGCTGAGA | 50849 |
| rs32139804 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244658 | TGGACAACTTCAGAA[A/G]AAACATCCAGATCAC | 50849 |
| rs32139805 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115244686 | CACTGTTGTGGCCAC[A/G]ATGCCCTGGCAGTCA | 50849 |
| rs32139806 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115244830 | CTAGGCGGTGGGCAC[C/T]GGGCAGTGGGCACCT | 50849 |
| rs32139807 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115244866 | CTCTCTTTCCTAGTA[G/T]CAGGTCCTTCCACAC | 50849 |
| rs32139808 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245108 | CCCCGTTCCTGCCAC[G/T]GAAGTTCCTGTAGAT | 50849 |
| rs32139809 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245394 | TTACAATCAATATTA[C/T]GAAAGGACATTATAA | 50849 |
| rs32139810 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115245401 | CAATATTATGAAAGG[A/G]CATTATAAACATTAA | 50849 |
| rs32139811 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115245452 | AGAACAGATGGGTCA[A/G]AAAAATGATGCAGGC | 50849 |
| rs32139812 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245605 | TTCAGACACTAGAGT[C/T]TGCTTATGACGGTCA | 50849 |
| rs32139813 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115246029 | AAAGGCAATGGAGGT[C/T]CATGTACACAGCTGG | 50849 |
| rs32140624 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115246093 | ACTATCAGGCTGTCT[A/C]TGCTTTACAGTAATC | 50849 |
| rs32140625 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246126 | GACAGCAGGAGGCCC[A/G]GGCAGTAAGAGTAGC | 50849 |
| rs32140626 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115246138 | CCCAGGCAGTAAGAG[C/T]AGCCTAAGATATGTC | 50849 |
| rs32140627 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246146 | GTAAGAGTAGCCTAA[A/G]ATATGTCAGGATCCT | 50849 |
| rs32140628 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246210 | GTACCTTCACCTCTG[A/G]GGGGTAGGCAGTTCA | 50849 |
| rs32140629 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246253 | CCTAACTGAGCTACT[A/G]TCTCACAAACTTCTC | 50849 |
| rs32140630 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115246368 | CAGAGCAAGCTGTGC[C/T]GACCACTCTAATGGA | 50849 |
| rs32140631 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246486 | AGTGGGCATGAGCTC[C/G]CTCTGAGCCTGGAGT | 50849 |
| rs32140632 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246589 | GTCAAATCAGAAACT[A/G]TTCCCAGCTCAGCAG | 50849 |
| rs32140633 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115246763 | GAACAGTTCATTATC[A/C]CCTTCACTATCTTAC | 50849 |
| rs32141444 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246872 | GCAACCGTGAGCTCT[A/G]AACTTACACCTGCCC | 50849 |
| rs32141445 | snp | A/G | | | missense | Rnf10 | Mm_Celera | 5:115246931 | TGCGCTCTCGGCGAC[A/G]CTCCTCGCGAGCCTT | 50849 |
| rs32141446 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247010 | AAGTTGTAAGAAAGA[C/T]GGATCAGCCACTGTT | 50849 |
| rs32141447 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115247020 | AAAGATGGATCAGCC[A/G]CTGTTAACTCTCCCT | 50849 |
| rs32141448 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247056 | ACCACAGCTAAGCCA[G/T]CGAGACAGCAGACCA | 50849 |
| rs32141449 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247093 | TGGGTGCATCCCGTG[C/T]GTGTCTCAGCATACA | 50849 |
| rs32141450 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247155 | AGCAGAGAAGGGCAA[A/T]GGGGCTTTCTCACCT | 50849 |
| rs32141451 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247366 | CCAGAACTAAATGGA[C/T]AGCGCTGCTGCCACT | 50849 |
| rs32141452 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf10 | Mm_Celera | 5:115247645 | GAGGGAATCTGGTCC[A/G]GAACACTGGAAACCA | 50849 |
| rs32141453 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115248209 | GACAGGACACCCTGC[A/T]CTGAACCCTAGCACA | 50849 |
| rs32142224 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248232 | CTAGCACAATCAGAG[A/G]GGCATGTGGGGCTAT | 50849 |
| rs32142225 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248370 | GATGAGAGCATCACC[A/G]CAAAAGCCAAGTAAT | 50849 |
| rs32142226 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115248571 | TACTTCTTTTCTCCA[A/G]AAAACCTCACCTCAG | 50849 |
| rs32142227 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248728 | CCGCTAAAGACAAGA[A/G]CTCTATCACACAAGC | 50849 |
| rs32142228 | snp | C/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115248952 | AGAGCTGCTGAGCTG[C/G]GTGAAGCCTGGCTTA | 50849 |
| rs32142229 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249198 | ACCCTAGGTCAACAC[C/G]AAGTCCCATGTTCTG | 50849 |
| rs32142230 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249296 | ACCACCCCTGGAAAA[A/G]GTGACAGATCTAGTC | 50849 |
| rs32142231 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115249330 | AGGACACAGCCAAGC[C/T]ACCATCTCTCCTTCA | 50849 |
| rs32142232 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249377 | AGGACAAGTCACTTC[A/G]TTGTGATGGGCACAC | 50849 |
| rs32142233 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249609 | AGCTTAAGAATCCCT[A/G]ATGCAGAGGACACAG | 50849 |
| rs32143214 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115249644 | TACTCCTTCCTTGGC[C/T]AATTCTACTTACTCC | 50849 |
| rs32143215 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249822 | CCCCACTGTTACAGT[A/G]AGTCAGGACAACCAT | 50849 |
| rs32143216 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115249839 | GTCAGGACAACCATT[C/T]GGGGCTGTGGCTTAG | 50849 |
| rs32143217 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249868 | AGCCCCGGAAAGTTT[A/G]AAGCTCTCCACAACA | 50849 |
| rs32143218 | snp | C/T | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115250039 | CTCTGCCAGCTGCTG[C/T]TCCAGCGCTCCTTTC | 50849 |
| rs32143219 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250203 | AGAAAATGGGACTAA[C/G]AGTGCAACCTCCTAG | 50849 |
| rs32143220 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250284 | GAAGACATCCCAGCC[A/G]CACCGCATGTTTACG | 50849 |
| rs32143221 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250336 | CATAGGTCTAGCCAT[A/T]CGGAAATGCTCAGGA | 50849 |
| rs32143222 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250337 | ATAGGTCTAGCCATT[C/T]GGAAATGCTCAGGAA | 50849 |
| rs32143223 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115250375 | TCCTAAGAATGAAGG[A/C]GGCACTGGCGACAGG | 50849 |
| rs32144184 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250588 | AAATCCACCAACAGA[C/G]GTGAGCCAAGCACAG | 50849 |
| rs32144185 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115250642 | AGTGAGCTGAGGACA[A/C]CTGACTACAGTTTAG | 50849 |
| rs32144186 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250996 | AACTGGCTTAGCCAA[A/G]GGCAAATTCTGATAT | 50849 |
| rs32144187 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251266 | GGGTCTCACCTACCC[C/T]GCAGTCTTACCTCTT | 50849 |
| rs32144188 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251486 | AATGACACACAGCGT[C/T]ATGGCTCTCAGACCT | 50849 |
| rs32144189 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115251499 | GTCATGGCTCTCAGA[A/C]CTGACTCAGGGCCAG | 50849 |
| rs32144190 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115251611 | GTAAAGAACACTTCC[A/G]CCCGTGCAGTCTGAA | 50849 |
| rs32144191 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251834 | TTCCTGGTTATGACT[C/T]CCTCAAAGAGGGGTA | 50849 |
| rs32144192 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115255230 | AATAAAGCTTTTTTT[C/T]TTAAAGACCAGTCAG | 50849 |
| rs32144193 | snp | C/T | | | missense | Rnf10 | Mm_Celera | 5:115255406 | CAGCAAAGTGAGCTG[C/T]GTAGTCTTGGTCTTC | 50849 |
| rs32144624 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255444 | ACAAATTGGCAGCTA[A/G]AAACAGCAGGAAAGA | 50849 |
| rs32144625 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115255707 | AAAATTAACCCAGAC[C/T]GATGAGACTCTCTCC | 50849 |
| rs32144626 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115255815 | TCCCCATCAAAATAC[A/C]CAGTGGTGCTTTAGT | 50849 |
| rs32144627 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256170 | TACATCCTCTCACAC[A/G]TGCAATTTAATTCTT | 50849 |
| rs32144628 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256700 | TCAGTTCTTCCTCTG[C/G]TAGGCTCAGCACATG | 50849 |
| rs33037825 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273593 | AAACAACATAGTACA[A/G]TTAAGTAAGGAGATG | 50849 |
| rs33095205 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115270474 | CTGGTACATCACAGC[A/G]AAAACTGGTCCCTAC | 50849 |
| rs33256286 | snp | C/T | 0.32 | 0.24 | missense | Rnf10 | Mm_Celera | 5:115257038 | TTCTCTTCCCCCAGC[C/T]GCCATGCCCACTGCC | 50849 |
| rs33411028 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf10 | Mm_Celera | 5:115243146 | CCAGACTGGCTTCAA[A/G]ATCACAAAAATCTGT | 50849 |
| rs33417836 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115270516 | AGGCAACTTCTACAC[A/G]TCCTCAGGTAGACCT | 50849 |
| rs33443020 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf10 | Mm_Celera | 5:115270915 | TGTTACTAAGTCTCC[G/T]GGAGTTCTTTGTGTA | 50849 |
| rs33523562 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115269918 | TGTAGGGAAAAATAG[A/G]TTAAAGAAAAGGTCA | 50849 |
| rs33571338 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf10 | Mm_Celera | 5:115270740 | ACTGTCAGCTCAAAG[C/T]TCCCCATCTGTCACA | 50849 |
| rs33610177 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf10 | Mm_Celera | 5:115257939 | GTAATGAGATCTGAC[A/G]CCCTCTTCTGGAGTG | 50849 |
| rs33637875 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf10 | Mm_Celera | 5:115262920 | TCAAAAAAATAAAGT[A/G]GAGACGCTAGAGAGA | 50849 |
| rs33639958 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273613 | GTAAGGAGATGCTAA[C/T]CAAACACGTTTCAAT | 50849 |
| rs33645836 | snp | G/T | 0.444444 | 0.157135 | utr-variant-5-prime | Rnf10 | Mm_Celera | 5:115272793 | GAGAGAGGGCTGGCT[G/T]TCTCGGTGCCGGGGA | 50849 |
| rs33739812 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273077 | CTAGCGGGTTCCTTC[C/T]TTTTGAGACAATGTT | 50849 |
| rs45956145 | snp | A/G | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241333 | CTGGCCTTGGGAGGC[A/G]GGCTGCTGTGAATAA | 50849 |
| rs46185357 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273646 | AAAAGCATCCCAGCT[C/T]GAGAGGGATAAAAGA | 50849 |
| rs47159960 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267151 | ATCAGATTACAACAA[C/T]TGACCACATAAGGAT | 50849 |
| rs47452653 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115267645 | TTATGAATGCTGCCC[A/G]GTGCTGCAGTTCTCG | 50849 |
| rs47741746 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245238 | CTCCGTAGGACTGGC[C/T]TGCCTGTAGGCAAGT | 50849 |
| rs48117995 | snp | C/T | | | utr-variant-5-prime | Rnf10 | GRCm38.p3 | 5:115272594 | AGCGGCAAGGTGGGG[C/T]TGTGGGGCCCAGAGG | 50849 |
| rs48966103 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115242623 | TGCCCTTGCCGTCTG[A/C]CCGCTCTCACCTTTC | 50849 |
| rs49195805 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115267380 | TTTTTGAAATGTTTT[C/G]TAGACAACTTGCCAG | 50849 |
| rs49628541 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266719 | GCCATGCAGATGCTA[A/G]GACTTAAACCTGCAT | 50849 |
| rs49759423 | snp | A/G | | | downstream-variant-500B | Rnf10 | GRCm38.p3 | 5:115241529 | TTCCAGCTCCTACAC[A/G]GAGGCTCACAATCAA | 50849 |
| rs50026758 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245146 | CTCAGGGTCTGTGCT[G/T]ACTAGTTTCTTATGT | 50849 |
| rs50066790 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115245213 | ACTCTTAATTCCGTC[A/G]GGAGAAGGTCTCCGT | 50849 |
| rs50093677 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266566 | GCATGGTGGCACACC[C/T]GTAACCCAGCACCTG | 50849 |
| rs51078979 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265384 | CAGTGGTGGCGCACG[C/T]CTTTAATCCTAGCAC | 50849 |
| rs51609581 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115266487 | GCCTATGGCCACCCA[A/C]CCTTCACCCAGCACC | 50849 |
| rs51852178 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266094 | ATAGAGACACACCAC[C/T]ACCACCACCACAGTG | 50849 |
| rs52106853 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265530 | AAAAGAAAGAAAGAA[A/G]GGAAAAAAAAAGAAA | 50849 |
| rs52159326 | snp | A/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271606 | CACTCTCTCTCTcac[A/T]cacacacacacacac | 50849 |
| rs52354938 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115265476 | TCAGGACAGCCAGGG[A/C]TACACAGAGAAACCC | 50849 |
| rs52425783 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115271604 | ATCACTCTCTCTCTC[A/T]CACACACACACACAC | 50849 |
| rs52579065 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265474 | TTTCAGGACAGCCAG[A/G]GCTACACAGAGAAAC | 50849 |
| rs211703355 | in-del | -/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273496 | ACCTGTGCATACGTG[-/T]TAAGATTTTTCATAC | 50849 |
| rs211738701 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115255519 | AATTACCCACCTCAG[A/C]GTTCAGATGCTGGCC | 50849 |
| rs211773923 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115265432 | GCGGATTTCTGAGTT[A/C]GAGGCCAGCCTGGTC | 50849 |
| rs211777243 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261584 | CCTACCTCAATCCAC[-/A]AATAAATAATATATA | 50849 |
| rs211844331 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243710 | CTGTATCCTGGCTTG[A/G]CTTTAATTCCCCATC | 50849 |
| rs211924711 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256534 | CACCTCCTCCTCCTC[C/T]TCACAATGGTGGCCC | 50849 |
| rs212275797 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267558 | TTATGTTGTTTCTGG[C/T]CCACTCTTAAACCTC | 50849 |
| rs212283492 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245738 | AGAGCACCAGGCATG[G/T]ATGTGGTACACATAT | 50849 |
| rs212325154 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115257861 | GGGTTTAAGAGCGCC[A/G]ACTGCCCTTCCAAAG | 50849 |
| rs212365405 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268913 | AAAACAAACATATCA[A/G]ATATATTTATGTAGT | 50849 |
| rs212678365 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271534 | TATTATTATATTATT[A/G]TAATAATATCATTAT | 50849 |
| rs212696814 | snp | A/C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263296 | AGCTGTCTGGTTTAC[A/C/G]GAGCTGATACACAGA | 50849 |
| rs212725008 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115246631 | TCCCTCCCTCTTTCC[C/T]TCTCCCTTTCCCTCT | 50849 |
| rs212762691 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115272972 | TGTAGTCTTTTACCT[A/G]CATCCGGGTCCTAGG | 50849 |
| rs212812506 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250546 | AAGCAGGTTCTGGTA[C/G]AGGGAAACCTTGTCT | 50849 |
| rs212948274 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242617 | CAGATCTGCCCTTGC[C/T]GTCTGACCGCTCTCA | 50849 |
| rs213094419 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250158 | CACACAGAACACAAC[C/T]GTCCCACACTTACTT | 50849 |
| rs213141751 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262630 | GCGCCACTAACATCC[A/G]GCATGACTAATGAGC | 50849 |
| rs213166998 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273885 | AAGAAGCAGAGACAG[A/G]AGACGGATGCCAGTG | 50849 |
| rs213277103 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115264431 | GGTGTGGTGGCACAC[A/G]CCTTTAATCCCAGCA | 50849 |
| rs213293469 | snp | A/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274667 | TTTTCAGTTTTTTGG[A/T]TGTTATTTTATTTTT | 50849 |
| rs213492565 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115266763 | AACTTAATTTTAGAG[-/C]CCCCTCTCTCCAGCC | 50849 |
| rs213649721 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269070 | TGGGGTCTGGTTCCT[A/G]AGACATGAAACTGTC | 50849 |
| rs213738652 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270034 | TACAGGTGGAAGGGC[G/T]TGAAGTCAGGTCTTT | 50849 |
| rs213815212 | in-del | -/AAG | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274284 | AGAGGCAGGGCAAAA[-/AAG]AAAGAAAAGAAAAGA | 50849 |
| rs213951418 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115248805 | CATTCCTGCTTGCTG[C/T]TGGAAAGCAGGGAGC | 50849 |
| rs214157353 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242928 | TTGGGGAGGCTGAGG[C/T]AGGAGGATTGCCTAC | 50849 |
| rs214265585 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243610 | GAGACACATTATTCG[A/G]GATGAAGTGTGCTGT | 50849 |
| rs214291360 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259862 | GAGTTCAGCATTTTA[C/T]TCTGCAAGATAGACA | 50849 |
| rs214383153 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264411 | AAGAAACATTATTAA[A/G]GCCGGGTGTGGTGGC | 50849 |
| rs214406299 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273795 | AGCTACTACCTCATC[C/T]AGCCGATGAGTGGAA | 50849 |
| rs214413282 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248150 | TTTGGAATGAAAAGT[A/G]AGATATCAGTACCCC | 50849 |
| rs214744547 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115245480 | GGCTTTACGAAGCCA[A/C]AAGATCTAAGAAGTC | 50849 |
| rs214796045 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263896 | AGGACCAACATGCCA[A/G]AGTGACTGCTACCAA | 50849 |
| rs214886853 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265343 | TAAAAGAAACACACC[C/T]GTAAAGAAAACATAT | 50849 |
| rs215094142 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266507 | CACCCAGCACCAAGC[C/T]ACTGTTGAGCATAGC | 50849 |
| rs215138474 | snp | C/T | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115250045 | CAGCTGCTGCTCCAG[C/T]GCTCCTTTCTCCTCC | 50849 |
| rs215162964 | in-del | -/ATG | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115262049 | GCTTTGTAGAACTTA[-/ATG]ATGACTGATTTCTAT | 50849 |
| rs215246051 | snp | A/G | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241293 | GGTGCCTTTCAGCAG[A/G]CCCCAGTGAGGCATG | 50849 |
| rs215246245 | in-del | -/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244300 | AGATGGGGAGGTGAA[-/C]GGAATCAGGCATGGA | 50849 |
| rs215402510 | snp | A/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241751 | GGCTACAAATGAATA[A/T]GCTTGTCGGGAAGGC | 50849 |
| rs215435983 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267410 | GGACACACTAGTGAA[C/T]AACCAGGGAGAAACG | 50849 |
| rs215470628 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271431 | TCTCTGCGGTGGAAT[A/G]ACTCCTGGCTAGACA | 50849 |
| rs215654595 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257810 | AAACTCAGGTCTCTG[A/T]AAGAACTCTCTGTTT | 50849 |
| rs215671496 | in-del | -/CT | | | intron-variant | Rnf10 | Mm_Celera | 5:115270885 | CTTCCAGGAGACCCC[-/CT]CTCCCACTCCCAGTG | 50849 |
| rs215685618 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115257669 | CAGTGCTTATGCACA[A/C]GGAGCATGCATAGCG | 50849 |
| rs216013200 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261121 | AGACTTCCAGATCCA[A/G]CGCTGGGAAGCTGAG | 50849 |
| rs216036503 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270958 | CTAGGCTCCTCCCCA[C/T]GCTCAGGTTCACTGG | 50849 |
| rs216054935 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115246833 | CAGGCAAGGGGCCAC[A/C]TAGACTCACACAAGG | 50849 |
| rs216167166 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247717 | TTCATGCAATAAATA[C/T]AATTTTGTACCAATA | 50849 |
| rs216183800 | in-del | -/ACAACATAGT | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273580 | CACCAACAAAGAGAA[-/ACAACATAGT]ACAGTTAAGTAAGGA | 50849 |
| rs216280171 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244647 | TTTTCTGTGGATGGA[C/T]AACTTCAGAAGAAAC | 50849 |
| rs216294508 | in-del | -/A | | | intron-variant | Rnf10 | Mm_Celera | 5:115258617 | GGTGACTTCCAACTT[-/A]AGAGATCTGCTTGCC | 50849 |
| rs216340978 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268819 | CCAAGGCTGTAGACT[-/G]AAAAGATCAAGAAAC | 50849 |
| rs216355129 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115270633 | TAATTTGAGGGGGGT[-/G]GGGGGGATGCTAAGG | 50849 |
| rs216487693 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263559 | TCACCCTGAAGCCAC[C/T]GTGGCCCCTTTGCTC | 50849 |
| rs216560068 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251889 | CCTGTACTGGTTGGT[G/T]TTGTGTCAACTTGAC | 50849 |
| rs216597472 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115264307 | GAAGTTGTTGCAATA[A/C]CCTTTGTAAACAGGT | 50849 |
| rs216678742 | snp | G/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273207 | TTAAAAAAAAGATGT[G/T]TGGGTGTCTGGCCTC | 50849 |
| rs216801545 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115267648 | TGAATGCTGCCCGGT[A/G]CTGCAGTTCTCGGGA | 50849 |
| rs216876066 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265519 | AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGGAA | 50849 |
| rs217036814 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266435 | AGACAGTAACTGGAA[C/T]TGAGAGTTGGAATGG | 50849 |
| rs217231933 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270154 | ATGCTGTCTGATATG[C/T]CACAAGCTTTGGCCT | 50849 |
| rs217301481 | in-del | -/GGGGGGGG | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273713 | GGACGAATGGAATTT[-/GGGGGGGG]GGGGGGGGGGGGCTG | 50849 |
| rs217311492 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115260028 | GGCCCCAGGTCTGGT[C/T]CATCCCCAGCTGCAC | 50849 |
| rs217325407 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270860 | GCACTGGAAAACTAC[G/T]GGGTGTGCTCTTCCA | 50849 |
| rs217392176 | snp | G/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260983 | CCTGAGCACTGAGCC[G/T]GCAGGCAGGAGCTCA | 50849 |
| rs217577176 | in-del | -/AGG | | | intron-variant | Rnf10 | Mm_Celera | 5:115248320 | TTCTGAGGTGAAGGT[-/AGG]AGGATCAGAAGATCA | 50849 |
| rs217722492 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271997 | GGTGAGTCACACAAA[A/G]CCAGGTCTTGAGGCC | 50849 |
| rs217949012 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115242100 | TTAGACAAGGGGAGG[A/C]ACAGTACTGTGGGCA | 50849 |
| rs217974947 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242763 | TGTCTACAGTCTGTC[A/G]TGGACATGACAGAGG | 50849 |
| rs218027429 | snp | A/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274411 | AGGAATCAGTTTAAA[A/T]TGACATGGAGATCCA | 50849 |
| rs218228990 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265840 | TTAAATTAGGCTCTC[A/G]CTCTACAGTTTAGGC | 50849 |
| rs218445302 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274809 | AATCAAACCCAGGTC[C/T]TCTGGAAGAGTAGCT | 50849 |
| rs218574743 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271018 | TGCTGACATGTATAT[A/G]CACATGCATACAGAT | 50849 |
| rs218574777 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258818 | GCTGGGATTTGAACT[C/G]AGGACCTCTGGGAGA | 50849 |
| rs218644051 | snp | A/G | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241347 | CGGGCTGCTGTGAAT[A/G]AGAAGCTCCCATATA | 50849 |
| rs218818913 | in-del | -/TT | | | intron-variant | Rnf10 | Mm_Celera | 5:115262467 | ACTAAGAAGACAAAC[-/TT]CAGGAAATTGTTGCC | 50849 |
| rs218918022 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273430 | CATTCTGTGAAGAAT[A/G]TGGAGAGTCTTGGAG | 50849 |
| rs219035412 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261158 | GAACTGCCGACGAAC[-/T]TAAGATCAGTCCGGG | 50849 |
| rs219170825 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115248861 | AGTGCCAGGCCATCC[C/T]TCTCCTTCAAATACC | 50849 |
| rs219372545 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252221 | TTCCTGACCTGCTTG[A/G]GTTCCAGTCCTGGCT | 50849 |
| rs219685382 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115242998 | TATGGGGCATAGAGA[A/C]CTTAAGGATATACTG | 50849 |
| rs219740421 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252042 | CCTCCATGAGATCCA[A/G]CTCTAAGGCATTTTC | 50849 |
| rs219763939 | in-del | -/TACTT | | | intron-variant | Rnf10 | Mm_Celera | 5:115256609 | AGGGAAGCAGCCCAG[-/TACTT]TACTTGGAGTCAGCG | 50849 |
| rs219936200 | in-del | -/ACAA | | | intron-variant | Rnf10 | Mm_Celera | 5:115246257 | CTGAGCTACTATCTC[-/ACAA]ACAAACTTCTCTTGA | 50849 |
| rs219969632 | snp | G/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241541 | CACGGAGGCTCACAA[G/T]CAAATGTAGAGTGAC | 50849 |
| rs219970014 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250802 | ATTCTCCTGCCTCAG[C/T]CTCCCAAGTGCAGAG | 50849 |
| rs220011534 | in-del | -/TAGC | | | intron-variant | Rnf10 | Mm_Celera | 5:115271518 | ATAATCAGTAAGTAG[-/TAGC]TATTATTATATTATT | 50849 |
| rs220074302 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242220 | GCATGCACATGGTAC[A/G]CACACATAATAAAAA | 50849 |
| rs220228497 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273612 | AGTAAGGAGATGCTA[A/G]TCAAACACGTTTCAA | 50849 |
| rs220272203 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243872 | AGCTCTGTCCTGAGC[C/T]AATCTCTCAGCACTG | 50849 |
| rs220317877 | in-del | -/CGCACTAA | | | intron-variant | Rnf10 | Mm_Celera | 5:115263691 | CTTTATAGCAGTGAG[-/CGCACTAA]CCCTTCGTAGGGGGT | 50849 |
| rs220350796 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274184 | CTGATTTGATCCTCA[A/G]TATCATAAATGGGAA | 50849 |
| rs220374212 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115244821 | CAGACACTGCTAGGC[A/G]GTGGGCACTGGGCAG | 50849 |
| rs220448443 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256087 | GGGGCTTCCAGCTGC[C/T]GTAACTGCAGCTCGC | 50849 |
| rs220458041 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115244879 | TAGCAGGTCCTTCCA[C/T]ACCCACCCAATGCTA | 50849 |
| rs220572623 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258985 | CACTGTATAGTCAAA[A/T]GTAGAGGTTTTTAGC | 50849 |
| rs220621773 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260416 | AAATAAGGGGAAATA[A/G]GCCTTTCCACAGCCT | 50849 |
| rs220674779 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115260103 | CAGTGCCAGAAAGGC[C/T]ATTCTCTCTCCATAC | 50849 |
| rs220675108 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115247150 | TTCTGAGCAGAGAAG[A/G]GCAATGGGGCTTTCT | 50849 |
| rs220696244 | in-del | -/ATATAG | | | intron-variant | Rnf10 | Mm_Celera | 5:115264631 | ACAGGGCATATATAT[-/ATATAG]ATATAGATATAGATA | 50849 |
| rs220818688 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115248519 | TGCAGCCTCACTCCG[A/T]TGAGGCCTACACGAA | 50849 |
| rs221225037 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261200 | ATTCCAGGACAACTT[C/T]ATTATAAAAATAAAA | 50849 |
| rs221315181 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270433 | CAGAGGCGAGTTACA[C/T]TAACACCTGCTTAGA | 50849 |
| rs221359592 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249243 | GCAGCAGAGGCAGCT[A/G]TGCTCCCCAGGTGTT | 50849 |
| rs221378115 | in-del | -/CA | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273260 | GTATACAGACATACT[-/CA]CATATAGACAAAACA | 50849 |
| rs221950874 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258032 | CTCCTGAACCTTCTC[A/G]CCAACTCCACACACC | 50849 |
| rs221954922 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267753 | ACTATGCAGCAAGGC[C/T]AAGTCTAAGAAATTA | 50849 |
| rs221965168 | in-del | -/ATATATAT | | | intron-variant | Rnf10 | Mm_Celera | 5:115264623 | AAAAAGTTACAGGGC[-/ATATATAT]ATATATATATATAGA | 50849 |
| rs221984628 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257229 | ACTGACAGCAGAAAT[C/T]GGCACAGCTCCGCTT | 50849 |
| rs222059446 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246067 | TGCTCTAAGGGCCTG[A/G]GAGACAAATGACTAT | 50849 |
| rs222109271 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258365 | CCCACTCCTCTCGAA[C/T]GTCCGTCTGTCCGTC | 50849 |
| rs222114196 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115260059 | AGCCAGCCTAGTGCC[C/T]GCTCTGCACGCACTC | 50849 |
| rs222119974 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264128 | ACCCGAGCCTAGTCT[A/G]AGGCCTGACTGTCTC | 50849 |
| rs222135031 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250835 | CTCATGTGTGCACTA[C/T]CATGGCTGGTTTCTT | 50849 |
| rs222185854 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252337 | AGGAATAGAAACCCT[A/G]ACTAAGACAAATTGG | 50849 |
| rs222219972 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264794 | AAAATTCTGGCTTTA[A/G]GGGCTGGAGAAATGG | 50849 |
| rs222221055 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251233 | CTGGATGAAGCAGAG[C/T]GGGGAGACAGCAGCC | 50849 |
| rs222276947 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115262829 | CAGGGGAGGTAGACG[A/C]AGTTGATTCCAGGGG | 50849 |
| rs222368942 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115250936 | GGTCCTGTGCCACAT[-/C]CCTCTGCCCTTGTTT | 50849 |
| rs222380482 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261260 | TTTTGCATGTGTGTA[C/T]GTGTTTATTTACACG | 50849 |
| rs222414302 | snp | A/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252959 | GCAGCCTCAGTTGCA[A/T]TTGAAGGCCCAGGAC | 50849 |
| rs222439766 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115268180 | GACACAACTCAGTGA[C/T]CAAGTCCCTGCCTAA | 50849 |
| rs222454603 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266842 | AGAGAGAAAACACAT[C/T]CCCCAAATCTTGTTA | 50849 |
| rs222459051 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250224 | AACCTCCTAGAAATA[G/T]AACAATTACCCTAAA | 50849 |
| rs222509356 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258935 | CAAAAGAAGAAAAAG[A/T]AAAGGAACTCCAGCA | 50849 |
| rs222565945 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115269242 | AGTCACATCTCCTTC[G/T]CTAGCAGACCTCTCA | 50849 |
| rs222597996 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261215 | CATTATAAAAATAAA[A/G]TCTGTATTTTTTTTA | 50849 |
| rs222676744 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258861 | CTTAACTGCTGAGCC[A/T]TCTCTCCAGCCCCTC | 50849 |
| rs222871245 | in-del | -/TGAC | | | intron-variant | Rnf10 | Mm_Celera | 5:115243038 | GGGGTTTTGTCTGTT[-/TGAC]TGATTGATTGTTTTC | 50849 |
| rs223354060 | in-del | -/A | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271282 | CCAAAAGACTGATTG[-/A]AAAAAAAAATTACTA | 50849 |
| rs223367669 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265532 | AAGAAAGAAAGAAAG[A/G]AAAAAAAAAGAAAAA | 50849 |
| rs223504590 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255878 | CTCAGCAAAGGGGAA[A/G]GGAGGGGTAGAGACC | 50849 |
| rs223665277 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255031 | AAAAGCCTTCCATAT[C/G]CTAACTGGTATCAAA | 50849 |
| rs223696314 | in-del | -/AAGTC | | | intron-variant | Rnf10 | Mm_Celera | 5:115267476 | CAGATTTTGGAAAAT[-/AAGTC]AAGTTTCTAGAAGAA | 50849 |
| rs223702011 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115270476 | GGTACATCACAGCGA[A/C]AACTGGTCCCTACCC | 50849 |
| rs223759700 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269494 | TAGCTCTGTAGACCA[A/G]GCTGGCCTCAAACTC | 50849 |
| rs224011976 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115270382 | TTTACAATAAAACTA[A/C]ACATGTGCAAAACTC | 50849 |
| rs224080325 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264223 | GGTATATCCATGAAG[A/T]ATCTGTGAGTGGATG | 50849 |
| rs224132895 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273647 | AAAGCATCCCAGCTT[A/G]AGAGGGATAAAAGAG | 50849 |
| rs224161879 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265077 | ACCCCAGGTTTGGTT[C/T]CTAGCACTTACAAGT | 50849 |
| rs224417021 | in-del | -/AT | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115262169 | AACAAATGGCTTCTG[-/AT]GTTACTTTACTTAGA | 50849 |
| rs224452319 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115271183 | AGAAGCAGAGGCAGG[C/T]GGATCTCTGAGTTCA | 50849 |
| rs224455149 | snp | A/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115272258 | CCGCCGGCTCTTACC[A/G]CTCTTGGGTTTAGAC | 50849 |
| rs224526284 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270827 | CATCTTTGCACTAAA[C/T]ACATCCAGTGATGTT | 50849 |
| rs224543926 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271160 | GTCTGAGATTTTGGA[C/G]GTGCTTGAGAAGCAG | 50849 |
| rs224583483 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262885 | AAAGGCAACTTCCCA[A/G]ATCAGTGAGAGATAC | 50849 |
| rs224740811 | in-del | -/AAG | | | intron-variant | Rnf10 | Mm_Celera | 5:115267626 | CACTTCCAGGGCTTT[-/AAG]ATTATGAATGCTGCC | 50849 |
| rs224816798 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243743 | CTGCTCACCACTCAA[A/G]TGCTGGGATTTCAGG | 50849 |
| rs224843855 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115266002 | CAGCACAAGCTTATC[A/C]TACAGCAGGCTAAAG | 50849 |
| rs224979518 | snp | G/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274558 | CAACCATCTGTAAGG[G/T]GATCCACTGCCCTCT | 50849 |
| rs225182362 | in-del | -/CAAA | | | intron-variant | Rnf10 | Mm_Celera | 5:115264744 | ATAGAAACCCTGTCT[-/CAAA]CAAACAAACAAACAT | 50849 |
| rs225210069 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266734 | GGACTTAAACCTGCA[A/T]TCTTTGGAAGAGGAA | 50849 |
| rs225350161 | snp | C/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241579 | GCAGGGGCCAACAGA[C/T]AGGCATGCAAACACC | 50849 |
| rs225353243 | in-del | -/AAGAA | | | intron-variant | Rnf10 | Mm_Celera | 5:115245426 | ATTAAACATGGGAAT[-/AAGAA]AAGAGAAAACAGAAC | 50849 |
| rs225488280 | in-del | -/CACACATGGTACG | | | intron-variant | Rnf10 | Mm_Celera | 5:115242220 | CATGCACATGGTACA[-/CACACATGGTACG]CACACATAATAAAAA | 50849 |
| rs225556456 | in-del | -/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273178 | TCGCCAGTGCTTGGA[-/T]TTTTTTTCTTTTTTT | 50849 |
| rs225591606 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244429 | GAACGCAGACAAGAG[A/G]CTTCTCAAAGCTCCT | 50849 |
| rs225660290 | snp | C/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241517 | GTTGGGCTCAGCTTC[C/T]AGCTCCTACACGGAG | 50849 |
| rs225682767 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242913 | CCAAGAATCACAGAA[-/T]TGGGGAGGCTGAGGC | 50849 |
| rs225717493 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115249376 | AAGGACAAGTCACTT[C/T]GTTGTGATGGGCACA | 50849 |
| rs225813916 | snp | G/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273460 | GGAAAACACTCAATG[G/T]CAGCCTCAGAACTCC | 50849 |
| rs226035212 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115268844 | AGAAACTCCTGGTAG[C/T]CAGATTTACCTATGA | 50849 |
| rs226098205 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267526 | TTGTCTTCTCCATTT[C/T]TTTGTTTTCATTTTT | 50849 |
| rs226121493 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269650 | TTTATGACTGTGGAG[A/G]CAGAAGACAGTATCA | 50849 |
| rs226197794 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250432 | ATATTCTAGTTTTTA[A/T]AAGAACAATAGGGGC | 50849 |
| rs226200927 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243005 | CATAGAGACCTTAAG[C/G]ATATACTGTGTCTCC | 50849 |
| rs226431320 | snp | A/C | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273975 | GCCAGCCTGGTCTAC[A/C]GAGCAAGTTTCAGGT | 50849 |
| rs226480138 | in-del | -/AG | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115264639 | TATATATATATAGAT[-/AG]ATAGATATAGGTGCC | 50849 |
| rs226493430 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258511 | CCAGCTGTCCAGCTG[A/T]GTTCTCCCCAACAGA | 50849 |
| rs226649477 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246386 | CCACTCTAATGGAAG[C/G]AAGCAGGGAGCCAGG | 50849 |
| rs226872172 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115266410 | CAAGGCACGTTCACT[-/C]CTTAACTGCAGACAG | 50849 |
| rs227123176 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271065 | TGAAGGAGATTAGCG[C/G]AAGGTTACACAGGAA | 50849 |
| rs227583284 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251644 | AGAATGTCCCCGATT[C/T]GGTGGACTGTTTGAA | 50849 |
| rs227592629 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115248796 | CAGGCCCACCATTCC[C/T]GCTTGCTGCTGGAAA | 50849 |
| rs227741005 | in-del | -/GC | | | intron-variant | Rnf10 | Mm_Celera | 5:115266526 | GTTGAGCATAGCGCA[-/GC]GCCACTGTAGCAGGT | 50849 |
| rs227895746 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264331 | AACAGGTCCTCTTTT[C/T]CCCCTATTCTTTCTT | 50849 |
| rs227960519 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115255152 | GGTGGCTCACAACCA[C/T]CCGTAATGAGATCTG | 50849 |
| rs228073001 | in-del | -/TTTAC | | | intron-variant | Rnf10 | Mm_Celera | 5:115258902 | TTTTTAATGCCATTA[-/TTTAC]TTTAATGTGCAAGCA | 50849 |
| rs228094478 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256127 | CAAGTCTGCCCACCT[C/T]CAACTCAGGTGCACA | 50849 |
| rs228205168 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243274 | GAAAACCCTACAGTG[C/T]TTTTTGCACATGCAT | 50849 |
| rs228234569 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115247453 | AGGCCACAGGGAGTA[A/G]ACAGCCTGCTAACAG | 50849 |
| rs228282295 | in-del | -/AA | | | intron-variant | Rnf10 | Mm_Celera | 5:115245538 | CTTAGGACTAACTCT[-/AA]AAGTCTTTCACTTAA | 50849 |
| rs228357850 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115255110 | TGCTCTTCCAAAGGT[A/C]CTGAGTTCAAATCCC | 50849 |
| rs228363646 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259340 | TCTCAGCCCTTAGGA[C/T]GCCAACGCAGCGGCC | 50849 |
| rs228469758 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262947 | GAGAGTCTCCCGCCC[A/G]TCACTGATGTCTATC | 50849 |
| rs228679219 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250373 | TCTCCTAAGAATGAA[A/G]GAGGCACTGGCGACA | 50849 |
| rs228898297 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115246590 | TCAAATCAGAAACTA[C/T]TCCCAGCTCAGCAGA | 50849 |
| rs228924459 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266998 | TAGATCTGGATGATC[G/T]CGGAGTTCCACACTG | 50849 |
| rs228979625 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266347 | AATCAAGCTAACAAG[C/T]TACAGAGGATGGCAG | 50849 |
| rs229004612 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257651 | AAAATTAATTGAAAA[C/T]TTCAGTGCTTATGCA | 50849 |
| rs229072934 | in-del | -/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115266859 | CCCAAATCTTGTTAT[-/C]TGAAGCTGACAGAAC | 50849 |
| rs229281218 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260784 | GAGTTAACACATACA[C/T]GCTGAGCTCCAGGAG | 50849 |
| rs229353059 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115268957 | ACCACTTACAAACTT[A/C]CACAGCTTACAGATG | 50849 |
| rs229397176 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265363 | AGAAAACATATCCAG[A/G]CCAGGCAGTGGTGGC | 50849 |
| rs229439840 | in-del | -/GAGGAGGAG | | | cds-indel | Rnf10 | GRCm38.p3 | 5:115272639 | GAGGAGGACGAGGAC[-/GAGGAGGAG]GAGGAGGAGGAGGCC | 50849 |
| rs229440057 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259474 | CCCTGCCTACACTGG[C/T]TAATCCAATAAGCAC | 50849 |
| rs229473396 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115269821 | ATCAATGCCAGGCCC[G/T]AAGATGGTGCCTTGC | 50849 |
| rs229583776 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260566 | GAGTGTATACAGAGC[C/T]CTACAGAGGAAGGAC | 50849 |
| rs229701285 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115271050 | TGTGAAAGAAGGACA[C/T]GAAGGAGATTAGCGG | 50849 |
| rs229702806 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115262127 | TAATAACAGTAGCAA[-/C]TTGAATAAACTTTGT | 50849 |
| rs229762895 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271648 | CACCATGAAAGCCAA[A/G]CCCATATAACCTACC | 50849 |
| rs229808015 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263500 | TCAACTTTGTTATAC[C/T]CAAGCCAAGATTGAA | 50849 |
| rs229943484 | in-del | -/CGCT | | | intron-variant | Rnf10 | Mm_Celera | 5:115248101 | GTGTGTGCGTGCGCG[-/CGCT]CGCAGGCATATAAAA | 50849 |
| rs230109279 | snp | G/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273440 | AGAATGTGGAGAGTC[G/T]TGGAGGAAAACACTC | 50849 |
| rs230109519 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256219 | ACCTTTTTTTCCTTT[G/T]TGGATTTTGTTTAAG | 50849 |
| rs230135569 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115270916 | GTTACTAAGTCTCCT[-/G]GAGTTCTTTGTGTAG | 50849 |
| rs230182428 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115243368 | GTAAATCTGAACAGT[-/C]CCTCTGCCTTTACAA | 50849 |
| rs230219091 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264538 | ACTATACAGAGAAAC[C/T]CTGTCTCGAAAAACC | 50849 |
| rs230222526 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274745 | TAGATACCAGAAGAG[A/G]GGATTGTATACCCCA | 50849 |
| rs230285176 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273923 | TCTTTAATCTCAGCA[C/T]TCAGGAGGCAGATGC | 50849 |
| rs230363436 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115257544 | ACAGCTCCACCCCCT[-/C]CCCCCCAGCATTGGA | 50849 |
| rs230567602 | in-del | -/ACAA | | | intron-variant | Rnf10 | Mm_Celera | 5:115259395 | CTCAAGAATAAGTAG[-/ACAA]ACAAACAACTAAGAG | 50849 |
| rs230642571 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258762 | TCTTCAGACAAGGGT[A/T]TCAGATCTCATTACA | 50849 |
| rs230653306 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115270117 | AGCCATCCTACCTCA[A/C]TGAACTCTACTACCC | 50849 |
| rs230670256 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263966 | GAACCTTACCCTGCA[A/G]CTGCCTTCTGACTTA | 50849 |
| rs230721873 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269180 | CATTCTTCCGAGTCA[A/G]GACTCTGAAACAGTC | 50849 |
| rs230765649 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115272934 | TATATAGTTGCCAGG[C/T]GGGCGTGGTGCATTC | 50849 |
| rs230857198 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263217 | GAGAATGAATCCCAA[C/T]AGCCCTTCCATCACA | 50849 |
| rs230939332 | snp | A/G | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241759 | ATGAATATGCTTGTC[A/G]GGAAGGCGGCTCAAG | 50849 |
| rs231076134 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271462 | GGTTAAACGATTAGA[A/G]TAGTGCTATCACACC | 50849 |
| rs231202592 | in-del | -/AC | | | intron-variant | Rnf10 | Mm_Celera | 5:115257262 | TCCTCATGGCTGAGA[-/AC]ACTGAACCTCACCTA | 50849 |
| rs231315382 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264172 | TACCTCTGCTGATTC[A/G]TGTCTGCTAGCTCAA | 50849 |
| rs231322022 | in-del | -/AAGGAACTT | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241724 | CTGTCCCACTGGATG[-/AAGGAACTT]AAGGGCTACAAATGA | 50849 |
| rs231329726 | in-del | -/GAGA | | | intron-variant | Rnf10 | Mm_Celera | 5:115248051 | TGTGAGAGTGTGTGT[-/GAGA]GTGAGTGTGTGTGTG | 50849 |
| rs231382920 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242931 | GGGAGGCTGAGGCAG[G/T]AGGATTGCCTACAAT | 50849 |
| rs231438570 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115253034 | GACCACCAAGAGCAG[C/T]AGCAGCAGTGGAGTA | 50849 |
| rs231624613 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115243630 | AAGTGTGCTGTGCTA[A/C]GAGGTGCTGGCTTCA | 50849 |
| rs231784231 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270763 | CTGTCACACATGCTC[A/T]CTCTCACAAAAACAC | 50849 |
| rs231944653 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260759 | TCACAGACACGCTAT[A/G]GAAGCTACAGAGTTA | 50849 |
| rs232065618 | snp | A/C | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273788 | ACCTCTAAGCTACTA[A/C]CTCATCTAGCCGATG | 50849 |
| rs232198427 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270008 | TATCACCATCCTGTG[G/T]GTGCAGGATGTACAG | 50849 |
| rs232235098 | snp | G/T | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241325 | GTGTACTCCTGGCCT[G/T]GGGAGGCGGGCTGCT | 50849 |
| rs232328564 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115259714 | CAGCACAGCGAACTC[A/G]TCTTCTTGATAAGTA | 50849 |
| rs232369595 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243430 | GCTCTACTGTATTTC[A/G]TTTGCTAATGTGCCC | 50849 |
| rs232432604 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273809 | CTAGCCGATGAGTGG[A/G]ATTTTAGCAATCGTG | 50849 |
| rs232490707 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273227 | TGTCTGGCCTCCTAC[A/G]ATACCAAGCAAACAC | 50849 |
| rs232773143 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274469 | TTGCTAGAGAGATGG[C/T]TCGGAGGTTAAGAGC | 50849 |
| rs232852271 | snp | A/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115248678 | CACAAGGCAGCGCAC[A/G]TTGACAGGGTGCAGG | 50849 |
| rs232990099 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265214 | GCAGACAACAAGCTG[A/G]ATGTGGTAGCACACA | 50849 |
| rs233061759 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115271255 | GATGCAAAGAGAAAC[C/T]TGTCTCGAAAAACCA | 50849 |
| rs233403384 | snp | C/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241680 | AGGCACAGCCTCTTC[C/T]CAGGAGAAAAACCTG | 50849 |
| rs233522231 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267312 | GCCAACACGCAGCTG[A/T]GGACTGATCCTACTG | 50849 |
| rs233525461 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256669 | GAGGGCTCCTGGGAA[A/G]ACTTTTGTTTGCACC | 50849 |
| rs233790894 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255865 | TTACATCTAATGACT[C/G]AGCAAAGGGGAAGGG | 50849 |
| rs233891348 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256727 | CATGAGCACGGGAGT[C/T]AGAAACTCTCCTCTC | 50849 |
| rs233891680 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243790 | TTTATCTTTCACTAT[A/G]GTCATTTTATAAGAT | 50849 |
| rs233931470 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261491 | CAAGTAAGACAACTG[-/T]TAATTCCAGAACCAG | 50849 |
| rs234021232 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258091 | TTCATTCTGGCACAG[G/T]GAAGTTGTGGAGGGC | 50849 |
| rs234031572 | in-del | -/CACCAC | | | intron-variant | Rnf10 | Mm_Celera | 5:115266087 | ACAGAGATAGAGACA[-/CACCAC]CACCACTACCACCAC | 50849 |
| rs234147369 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115260053 | CTGCACAGCCAGCCT[A/G]GTGCCTGCTCTGCAC | 50849 |
| rs234166075 | snp | A/G | | | utr-variant-5-prime | Rnf10 | Mm_Celera | 5:115272811 | TCGGTGCCGGGGACC[A/G]GGGTCTCCGACACAG | 50849 |
| rs234267434 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260990 | ACTGAGCCTGCAGGC[A/G]GGAGCTCACTAGGCC | 50849 |
| rs234303542 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115247905 | AAGGGAGACAAAGCA[A/G]GGTGTAGTGGTGCAC | 50849 |
| rs234406867 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263720 | GTGGGGTGCGGACAA[A/G]GTTAGTTATAGCCTC | 50849 |
| rs234410539 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242384 | GTTGAGTGAGTTTCC[C/G]GCCCTTACCAGAGAG | 50849 |
| rs234457480 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115262839 | AGACGCAGTTGATTC[C/T]AGGGGCTTCATCAAC | 50849 |
| rs234486272 | in-del | -/AA | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115242231 | GTACACACACATAAT[-/AA]AAAAGAGTTCCTCAC | 50849 |
| rs234513310 | snp | G/T | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241370 | CCCATATAGCTAAAG[G/T]CTGTGGTCCCAGCTG | 50849 |
| rs234537888 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250723 | TCTTTAAGACAGAAT[C/G]CCATGAAGCTCAGAC | 50849 |
| rs234550672 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115250171 | ACCGTCCCACACTTA[A/C]TTCTTCTGCCCTAGG | 50849 |
| rs234698420 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115251894 | ACTGGTTGGTTTTGT[C/G]TCAACTTGACACAGC | 50849 |
| rs234889496 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245333 | GCCCAACCTATAAAA[A/T]TTTAATTAAGCCATT | 50849 |
| rs234903865 | in-del | -/TCTCTCA | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115256738 | AGTCAGAAACTCTCC[-/TCTCTCA]TCTCTCATCTCTCCC | 50849 |
| rs235019236 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115256331 | AGAGGGCATCAGATG[-/C]CCTGGACCTAAAGCT | 50849 |
| rs235033551 | snp | C/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252045 | CCATGAGATCCAACT[C/G]TAAGGCATTTTCTCA | 50849 |
| rs235483211 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248158 | GAAAAGTAAGATATC[A/G]GTACCCCAAACTGTA | 50849 |
| rs235612312 | in-del | -/CAGGCTTCCCTC | | | intron-variant | Rnf10 | Mm_Celera | 5:115251788 | TTGTCTGCCTACCGG[-/CAGGCTTCCCTC]CAAGGTAATCAAGGG | 50849 |
| rs235764450 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115247641 | TGCTGAGGGAATCTG[A/G]TCCGGAACACTGGAA | 50849 |
| rs235827125 | in-del | -/GC | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273725 | ATTTGGGGGGGGGGG[-/GC]TGTTAGGGATCAAAT | 50849 |
| rs235878932 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250815 | AGTCTCCCAAGTGCA[A/G]AGATCTCATGTGTGC | 50849 |
| rs235913764 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258832 | TCAGGACCTCTGGGA[A/G]AGCAGTCAGTGCTCT | 50849 |
| rs236033964 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115262925 | AAAATAAAGTGGAGA[C/T]GCTAGAGAGAGTCTC | 50849 |
| rs236062775 | snp | A/G | | | utr-variant-5-prime | Rnf10 | Mm_Celera | 5:115272713 | GAGGCTGCGGGGGAA[A/G]GGGAGGCGCGGGAGG | 50849 |
| rs236110052 | in-del | -/CACACACC | | | intron-variant | Rnf10 | Mm_Celera | 5:115271629 | ACACACACACACACA[-/CACACACC]ATGAAAGCCAAGCCC | 50849 |
| rs236160432 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258790 | ACAGATGGTTGTGAG[C/T]CACCATGTGGTTGCT | 50849 |
| rs236162264 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263976 | CTGCAGCTGCCTTCT[A/G]ACTTACACTTATACA | 50849 |
| rs236168632 | snp | C/T | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115242015 | GACCGAGGTGCTGAA[C/T]AGCAGCTTCTGCTTC | 50849 |
| rs236394527 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265676 | TGTGTGGAAATTTTC[A/G]TGTGTATACTAATCT | 50849 |
| rs236401492 | in-del | -/TTTT | | | intron-variant | Rnf10 | Mm_Celera | 5:115270596 | TTATAATTTTAGTGC[-/TTTT]TTTTTTTTTTTTTGC | 50849 |
| rs236405324 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266889 | CATGACTCTTAACTG[C/T]AGCTCTCAAGAGCTA | 50849 |
| rs236432213 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257730 | GGAAAGTCCCCGGAG[C/T]TCTTGGAGCCAGGGT | 50849 |
| rs236432219 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257823 | TGTAAGAACTCTCTG[C/T]TTGGGGCTGGTGAGA | 50849 |
| rs236436255 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267640 | TAAGATTATGAATGC[C/T]GCCCGGTGCTGCAGT | 50849 |
| rs236447070 | in-del | -/ATATAT | | | intron-variant | Rnf10 | Mm_Celera | 5:115264624 | AAAAAGTTACAGGGC[-/ATATAT]ATATATAGATATAGA | 50849 |
| rs236605576 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115267771 | GTCTAAGAAATTAAG[A/G]AAAAAGAGAGGTGGG | 50849 |
| rs236622207 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252366 | GGTACCAGCAGAGTG[G/T]GGTATTCCTGTGACA | 50849 |
| rs236724292 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270971 | CACGCTCAGGTTCAC[A/T]GGTGGATATGCATAG | 50849 |
| rs236956062 | in-del | -/TTGACTGA | | | intron-variant | Rnf10 | Mm_Celera | 5:115243037 | AGGGGTTTTGTCTGT[-/TTGACTGA]TTGATTGTTTTCTTT | 50849 |
| rs237005091 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115269102 | CAGAAACCAAACACA[-/T]TTTTGTGTGTTTTTC | 50849 |
| rs237155963 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250816 | GTCTCCCAAGTGCAG[A/G]GATCTCATGTGTGCA | 50849 |
| rs237228826 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258896 | ACCTGTTTTTTAATG[C/T]CATTATTTACTTTAA | 50849 |
| rs237340312 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247018 | AGAAAGATGGATCAG[C/T]CACTGTTAACTCTCC | 50849 |
| rs237392316 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115248833 | AGCCGACCCCCAGGA[A/C]GGCTCTGTTCAGAGT | 50849 |
| rs237397394 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263900 | CCAACATGCCAGAGT[A/G]ACTGCTACCAAATCT | 50849 |
| rs237604073 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115251942 | AAGGACCTTCAGTTG[A/G]GGAAATGCCTTGTAT | 50849 |
| rs237656431 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115264415 | AACATTATTAAGGCC[A/G]GGTGTGGTGGCACAC | 50849 |
| rs237747828 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115243147 | CAGACTGGCTTCAAG[A/C]TCACAAAAATCTGTC | 50849 |
| rs237924431 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258842 | TGGGAGAGCAGTCAG[A/T]GCTCTTAACTGCTGA | 50849 |
| rs238001069 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268988 | CCGAGGGAGGGAGAG[A/G]CTAAGCCATGGTGGT | 50849 |
| rs238240651 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266522 | CACTGTTGAGCATAG[C/T]GCAGCGCCACTGTAG | 50849 |
| rs238263479 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115248396 | GTAATAGTCTGAGGC[C/T]ACCCTGCCCTACAGA | 50849 |
| rs238398786 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270473 | ACTGGTACATCACAG[C/T]GAAAACTGGTCCCTA | 50849 |
| rs238438367 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256875 | AAATGTGACAGGGGG[A/G]AGAGAAGGACACTTT | 50849 |
| rs238457186 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269662 | GAGGCAGAAGACAGT[A/G]TCAAATTCCACAGCA | 50849 |
| rs238510239 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115242277 | ACCTTAAGGATTCAC[A/C]TAGGGTGGACAATAA | 50849 |
| rs238532619 | snp | A/C | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241556 | TCAAATGTAGAGTGA[A/C]TCCAGTTGCAGGGGC | 50849 |
| rs238607124 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263585 | GCTCCTTTACTTTCA[-/T]TTTTTTTACTTAAAC | 50849 |
| rs238695153 | snp | C/T | | | missense | Rnf10 | Mm_Celera | 5:115272329 | GCCCTTTGCTGCTGC[C/T]CGAGGAGGCGGAGGA | 50849 |
| rs238750340 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115262517 | ATAAGTTTTTTTTTT[-/C]CCTTTTTTGAGACAA | 50849 |
| rs238753352 | in-del | -/A | | | intron-variant | Rnf10 | Mm_Celera | 5:115266808 | AAAGAAAAAAGGGGG[-/A]AAAAAAGCAAAGAAA | 50849 |
| rs238833534 | snp | G/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274214 | AAGGAACAAGAATGT[G/T]CGGGCCAAGCCAGGC | 50849 |
| rs238845475 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115270414 | AGAATCAGTTTATAC[A/G]GTTCAGAGGCGAGTT | 50849 |
| rs238860347 | snp | A/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274022 | GAAAAACCTTGTCTC[A/T]AAAAAATAAATAAAT | 50849 |
| rs238865926 | in-del | -/TT | | | intron-variant | Rnf10 | Mm_Celera | 5:115267936 | ATGCTCAAATGATAA[-/TT]TTTTTTTTTTTTTTT | 50849 |
| rs238925558 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266482 | TACAGGCCTATGGCC[A/G]CCCAACCTTCACCCA | 50849 |
| rs239152487 | in-del | -/AAAAAAAAAAA | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115267181 | TTTATGATTTCAGGC[-/AAAAAAAAAAA]AAAAAAAAAAAATCA | 50849 |
| rs239405458 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115270189 | CTCACTGAACAATAA[A/G]TAAAGCATTTATTGC | 50849 |
| rs239578888 | in-del | -/TCTGCCCTTGCCG | | | intron-variant | Rnf10 | Mm_Celera | 5:115242605 | GAGGGGTTGTCCAGA[-/TCTGCCCTTGCCG]TCTGCCCTTGCCGTC | 50849 |
| rs239829950 | in-del | -/A | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261688 | AGAAGACCTAAGTTC[-/A]GCTTAGCACCCACAT | 50849 |
| rs239830203 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115272171 | GCAGATCGGCTTAAC[A/C]GTAAATACTGGATGT | 50849 |
| rs239887208 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115267660 | GGTGCTGCAGTTCTC[A/G]GGAGGTTGAGGACAG | 50849 |
| rs239992381 | in-del | -/A | | | intron-variant | Rnf10 | Mm_Celera | 5:115255516 | GGAATTACCCACCTC[-/A]AGAGTTCAGATGCTG | 50849 |
| rs240278410 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243012 | ACCTTAAGGATATAC[C/T]GTGTCTCCCAGGGGT | 50849 |
| rs240316453 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115254394 | TTGCTATTTTGGAGT[C/G]TGATTATGTATTTTA | 50849 |
| rs240493571 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115257241 | AATCGGCACAGCTCC[C/G]CTTCCTTCCTCATGG | 50849 |
| rs240566277 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115269386 | CAGTGAGTGCTGGGA[G/T]TACAGGCTGTCCCCA | 50849 |
| rs240632576 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115268325 | GTCCACACAATCATC[G/T]GTGACTGTACAGGAA | 50849 |
| rs240635276 | snp | A/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273193 | ATTTTTTTCTTTTTT[A/T]AAAAAAAAGATGTGT | 50849 |
| rs240723300 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258939 | AGAAGAAAAAGAAAA[C/G]GAACTCCAGCAAAGG | 50849 |
| rs240746213 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268982 | CAGATGCCGAGGGAG[A/G]GAGAGGCTAAGCCAT | 50849 |
| rs240782216 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248532 | CGATGAGGCCTACAC[A/G]AAAGAGATCATGGTA | 50849 |
| rs240807682 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242764 | GTCTACAGTCTGTCG[A/T]GGACATGACAGAGGG | 50849 |
| rs241215326 | in-del | -/TTTT | | | intron-variant | Rnf10 | Mm_Celera | 5:115265817 | AAAAGAGGTAAGCAC[-/TTTT]TTTTTTTTTAAATTA | 50849 |
| rs241231681 | in-del | -/AACA | | | intron-variant | Rnf10 | Mm_Celera | 5:115266371 | TGGCAGCAGGAAGAG[-/AACA]AACAGGTTACCACAC | 50849 |
| rs241244070 | in-del | -/CACACACACACACACA | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271603 | CATCACTCTCTCTCT[-/CACACACACACACACA]CACACACACACACAC | 50849 |
| rs241260413 | snp | A/C | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274823 | CCTCTGGAAGAGTAG[A/C]TAGTGTTCTTAATTG | 50849 |
| rs241450474 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265523 | AAAAAAAAAAAGAAA[A/G]AAAGAAAGGAAAAAA | 50849 |
| rs241511770 | snp | C/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241673 | AATCAACAGGCACAG[C/T]CTCTTCCCAGGAGAA | 50849 |
| rs241728661 | snp | A/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261354 | GGGGTCTGGAAAAAA[A/T]TAAGCTCAGTCACCT | 50849 |
| rs241905437 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115270863 | CTGGAAAACTACGGG[C/G]TGTGCTCTTCCAGGA | 50849 |
| rs242034299 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248304 | AAACAGCCCTGAGCA[C/G]TTCTGAGGTGAAGGT | 50849 |
| rs242187899 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258369 | CTCCTCTCGAACGTC[C/T]GTCTGTCCGTCTGTC | 50849 |
| rs242200831 | in-del | -/A | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241613 | TCGGAGGCCTTTAAG[-/A]AAAAGGGGCTGTGAA | 50849 |
| rs242284385 | in-del | -/TGGTGAG | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273398 | CCAGACTAGCTCAAA[-/TGGTGAG]TCTACCTAGCCATTC | 50849 |
| rs242287763 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251046 | TTCATTAAGGGTCAG[-/T]CCCCCCCCCTCGTGC | 50849 |
| rs242290874 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115270126 | ACCTCACTGAACTCT[A/C]CTACCCTCTCTTATG | 50849 |
| rs242357187 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261332 | GGGTTCTGTCCTGCC[A/G]ATGTGCGGGGTCTGG | 50849 |
| rs242395512 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260724 | AAATTACAGGACAGC[C/T]AAGACAGAGAGACAT | 50849 |
| rs242407842 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260945 | CCCTGTCATAAACCT[A/C]AACTTTTCCTCCTGT | 50849 |
| rs242493115 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243045 | TGTCTGTTTGACTGA[C/T]TGATTGTTTTCTTTT | 50849 |
| rs242617392 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243714 | ATCCTGGCTTGGCTT[G/T]AATTCCCCATCCTCT | 50849 |
| rs242691227 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265861 | CAGTTTAGGCTAGCC[G/T]AGAACTCACTACCTC | 50849 |
| rs242694740 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115262212 | CTTTTTAAACCTGAA[-/T]TTCTCTTAATTAGCA | 50849 |
| rs242723105 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115255568 | CAGGATGGGGCTGCA[C/T]AACCCACAGACTTCA | 50849 |
| rs242732680 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255113 | TCTTCCAAAGGTCCT[A/G]AGTTCAAATCCCAGC | 50849 |
| rs242770450 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265150 | ACACATAAAACTTAC[C/T]TAACAAAAAAGGTCT | 50849 |
| rs242807439 | in-del | -/TG | | | intron-variant | Rnf10 | Mm_Celera | 5:115270004 | AATGTATCACCATCC[-/TG]TGGGTGCAGGATGTA | 50849 |
| rs242807761 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256940 | GGTGTCCTCCTCACA[A/G]TGTGGTCCCCCTTGC | 50849 |
| rs242846143 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256088 | GGGCTTCCAGCTGCT[G/T]TAACTGCAGCTCGCA | 50849 |
| rs242848129 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242337 | TGACCCAGGCAGGAA[C/G]GGCAGCACACGTGGC | 50849 |
| rs242872278 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266142 | GGACAACCTGCAGAG[A/G]TTGGTTCTCTCCTTC | 50849 |
| rs242914096 | in-del | -/TGTGTGGAAATTTTCG | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265661 | GCTTCAGGATTTTCA[-/TGTGTGGAAATTTTCG]TGTGTATACTAATCT | 50849 |
| rs242982883 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115251030 | CAAGATGCATGCACT[-/G]TTCATTAAGGGTCAG | 50849 |
| rs243049036 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264189 | GTCTGCTAGCTCAAC[A/T]CTACGGAACTGGACC | 50849 |
| rs243331584 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256010 | AGCAAACAAGTAAAT[A/G]CTAGAGTTGGCAGTT | 50849 |
| rs243337855 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242103 | ACAAGGGGAGGCACA[-/T]GTACTGTGGGCACCC | 50849 |
| rs243357669 | in-del | -/CGCGCT | | | intron-variant | Rnf10 | Mm_Celera | 5:115248099 | GTGTGTGTGCGTGCG[-/CGCGCT]CGCAGGCATATAAAA | 50849 |
| rs243442233 | snp | A/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115245885 | TGCTCAGAGGAGACA[A/G]GGATAGGGCCCCATG | 50849 |
| rs243776385 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269551 | AGTGCTGGGATTAAA[A/G]GTGTGGACCACCACG | 50849 |
| rs243888383 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259089 | GTGGGTGGTGGCACA[A/T]TCCTTTAATGTCAGC | 50849 |
| rs243915820 | snp | C/T | | | utr-variant-3-prime | Rnf10 | Mm_Celera | 5:115241857 | CTTGGTTCCCCCTCA[C/T]TTTGTGGAAAGCCCC | 50849 |
| rs243995916 | in-del | -/CAAC | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265753 | AGGAGGTTCCTGCAC[-/CAAC]TCACCCTCAAAGATT | 50849 |
| rs244020691 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242616 | CCAGATCTGCCCTTG[C/T]CGTCTGACCGCTCTC | 50849 |
| rs244168454 | snp | C/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274666 | TTTTTCAGTTTTTTG[C/G]TTGTTATTTTATTTT | 50849 |
| rs244286792 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115245473 | TGATGCAGGCTTTAC[A/G]AAGCCACAAGATCTA | 50849 |
| rs244317077 | in-del | -/GCCA | | | intron-variant | Rnf10 | Mm_Celera | 5:115251509 | CAGACCTGACTCAGG[-/GCCA]GCCAGCAAAGTCAGA | 50849 |
| rs244328808 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271168 | TTTTGGAGGTGCTTG[A/G]GAAGCAGAGGCAGGT | 50849 |
| rs244331132 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250974 | ACTTCTCATGCCGGT[A/G]GGTTAAAACTGGCTT | 50849 |
| rs244435711 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115267556 | TGTTATGTTGTTTCT[C/G]GCCCACTCTTAAACC | 50849 |
| rs244478940 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261415 | CGTCTCTCTGGACCA[C/T]GGGGAAATTCAATGG | 50849 |
| rs244560962 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268898 | ATAAGCTAGCCACAG[A/G]AAACAAACATATCAG | 50849 |
| rs244778091 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115271533 | GTATTATTATATTAT[A/T]ATAATAATATCATTA | 50849 |
| rs244843862 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245222 | TCCGTCGGGAGAAGG[C/T]CTCCGTAGGACTGGC | 50849 |
| rs244898216 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257573 | GAACACACAGGCAGG[A/T]GGATTTAAGTTGGAG | 50849 |
| rs244901393 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115272958 | TGCATTCTGGGAAGT[A/G]TAGTCTTTTACCTAC | 50849 |
| rs244952931 | in-del | -/A | | | intron-variant | Rnf10 | Mm_Celera | 5:115258840 | TCTGGGAGAGCAGTC[-/A]GTGCTCTTAACTGCT | 50849 |
| rs245234046 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266739 | TAAACCTGCATTCTT[C/T]GGAAGAGGAACTTAA | 50849 |
| rs245336396 | in-del | -/CTGCATCCCGA | | | intron-variant | Rnf10 | Mm_Celera | 5:115257318 | ACGCTCCCCTAGCAT[-/CTGCATCCCGA]CTGTCCCGTCGCCCT | 50849 |
| rs245467296 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259423 | TAAGAGTTCAGTCGC[G/T]TAGGCATGTCATTGC | 50849 |
| rs245907828 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115256565 | AGCTCCAAAAGTCCA[-/C]AGCCTAAGCAACACC | 50849 |
| rs245918173 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261943 | ACAGTACTGAAGATT[A/G]TTTTATAAGGTCTAT | 50849 |
| rs245990875 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248797 | AGGCCCACCATTCCT[A/G]CTTGCTGCTGGAAAG | 50849 |
| rs246059339 | snp | A/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115264979 | ACACATACAAACACA[A/C]ACACACACACACAGG | 50849 |
| rs246070423 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262972 | TCTATCTTCACATGT[A/G]CATTCAAGGGTGAGA | 50849 |
| rs246182504 | in-del | -/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115255230 | AATAAAGCTTTTTTT[-/C]TTAAAGACCAGTCAG | 50849 |
| rs246195582 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255066 | AGTCAGGGGGCTGGC[A/G]AGATGGCTCAGCGGG | 50849 |
| rs246204725 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251909 | GTCAACTTGACACAG[C/T]TGGAGTTATCACAGA | 50849 |
| rs246385702 | snp | A/G | | | utr-variant-5-prime | Rnf10 | Mm_Celera | 5:115272825 | CGGGGTCTCCGACAC[A/G]GCGACCGACACTCGC | 50849 |
| rs246424543 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256680 | GGAAAACTTTTGTTT[A/G]CACCTCAGTTCTTCC | 50849 |
| rs246435752 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115267027 | TGACAAGACTGAAGA[C/T]GAAGCAGCACTCAGG | 50849 |
| rs246476569 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243609 | TGAGACACATTATTC[A/G]AGATGAAGTGTGCTG | 50849 |
| rs246524945 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257661 | GAAAACTTCAGTGCT[G/T]ATGCACAAGGAGCAT | 50849 |
| rs246618024 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264946 | TTCTGGCCTCTGAAG[A/G]CACCTGGTATATATA | 50849 |
| rs246735838 | snp | C/G | | | missense | Rnf10 | Mm_Celera | 5:115242402 | CCTTACCAGAGAGGG[C/G]GTCTGAAGTAGCTGG | 50849 |
| rs246984887 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115253000 | ATGCAGTGTTTTGGA[A/G]ATACCAGTACCATGA | 50849 |
| rs247294345 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250288 | ACATCCCAGCCGCAC[C/T]GCATGTTTACGAATG | 50849 |
| rs247335479 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262897 | CCAGATCAGTGAGAG[A/G]TACAGTCTCAAAAAA | 50849 |
| rs247541737 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247942 | AACCCTAGAGCTCAG[C/T]CAGCCTCATCTACAC | 50849 |
| rs247689657 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266004 | GCACAAGCTTATCAT[A/T]CAGCAGGCTAAAGAC | 50849 |
| rs247785534 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266377 | GCAGGAAGAGAACAG[A/G]TTACCACACAAAACT | 50849 |
| rs247923769 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115245452 | AGAACAGATGGGTCA[-/G]AAAAATGATGCAGGC | 50849 |
| rs247945863 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115267821 | TGGGCCTAGTAGCAC[A/G]GGCCTGGGATCTCAG | 50849 |
| rs248035001 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269216 | ACTACCCACTGCTCC[A/G]TGCACATCTTAGTCA | 50849 |
| rs248086880 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243000 | TGGGGCATAGAGACC[A/T]TAAGGATATACTGTG | 50849 |
| rs248113234 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115259988 | CCCAGGGGTGTCACA[A/G]ACCCCCAGGGAGGAA | 50849 |
| rs248138219 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258819 | CTGGGATTTGAACTC[A/G]GGACCTCTGGGAGAG | 50849 |
| rs248157379 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246678 | CCAGATCCTGAATGT[-/G]GCCCCTGCCCTCCTG | 50849 |
| rs248221460 | in-del | -/CTCTCTCT | | | intron-variant | Rnf10 | Mm_Celera | 5:115271593 | TGACTACACACATCA[-/CTCTCTCT]CTCACACACACACAC | 50849 |
| rs248227202 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115248353 | GGCATCCTTGGCTCA[-/C]CGATGAGAGCATCAC | 50849 |
| rs248291711 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259668 | CTACTCAATCTGTCT[C/T]GCTACACACACAGCA | 50849 |
| rs248296215 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115258221 | AGAAATAAACCTAAT[-/C]GCTATGCTAATCACA | 50849 |
| rs248400343 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268549 | ACCTCCGCCTCGGGA[A/G]GAGGAACAAGAGCAG | 50849 |
| rs248504978 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115244985 | CTAGCACGAGGACTC[C/T]GCCCCATAGTGTACC | 50849 |
| rs248565220 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273697 | GTCATGTGACACACA[C/T]AGGACGAATGGAATT | 50849 |
| rs248577936 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273116 | TAGTCCTAACGGGAC[C/T]TGAACTCTTTGTGTG | 50849 |
| rs248697721 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264245 | GAGTGGATGGAGCTG[C/T]AGCTGCTAACCTGTG | 50849 |
| rs248808139 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115251932 | ATCACAGAGAAAGGA[C/G]CTTCAGTTGAGGAAA | 50849 |
| rs249110067 | in-del | -/A | | | intron-variant | Rnf10 | Mm_Celera | 5:115242274 | GGACCTTAAGGATTC[-/A]ACATAGGGTGGACAA | 50849 |
| rs249144901 | in-del | -/AC | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241350 | CTGCTGTGAATAAGA[-/AC]AGCTCCCATATAGCT | 50849 |
| rs249241776 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273517 | TTTTTCATACACGTA[C/T]GCATGCCACATTCAT | 50849 |
| rs249297918 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248834 | GCCGACCCCCAGGAA[A/G]GCTCTGTTCAGAGTG | 50849 |
| rs249395491 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264132 | GAGCCTAGTCTGAGG[C/T]CTGACTGTCTCTGCT | 50849 |
| rs249668274 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256528 | CCAAGGCACCTCCTC[C/T]TCCTCTTCACAATGG | 50849 |
| rs249854632 | snp | A/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115272393 | GGCGGTGGCGGCGGC[A/G]CTGGGGGAGCTCTGC | 50849 |
| rs249940230 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273367 | GATCTGGAAATTCCC[A/G]GAACAAACTGGCTAG | 50849 |
| rs249982943 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271063 | CATGAAGGAGATTAG[C/G]GGAAGGTTACACAGG | 50849 |
| rs249995855 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246348 | CATCCTCACTCCTCG[A/G]TCACCAGAGCAAGCT | 50849 |
| rs250132440 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242331 | TGCCACTGACCCAGG[C/T]AGGAACGGCAGCACA | 50849 |
| rs250240954 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242979 | AATATGAGTTTTAGG[A/G]TAATATGGGGCATAG | 50849 |
| rs250264799 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115246602 | CTATTCCCAGCTCAG[C/T]AGAGCTGTCTCTCTC | 50849 |
| rs250352935 | in-del | -/GGAACACACA | | | intron-variant | Rnf10 | Mm_Celera | 5:115255983 | CACATGCACACTAGG[-/GGAACACACA]GGAGCAAACAAGTAA | 50849 |
| rs250499067 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265834 | TTTTTTTTAAATTAG[C/G]CTCTCACTCTACAGT | 50849 |
| rs250617745 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266555 | GGTGGCAATCTGCAT[A/G]GTGGCACACCCGTAA | 50849 |
| rs250671417 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271099 | TTGGAGGGAGGAAAG[A/G]GAAGGAGAAACATTG | 50849 |
| rs250962922 | in-del | -/TC | | | intron-variant | Rnf10 | Mm_Celera | 5:115262516 | AATAAGTTTTTTTTT[-/TC]CCTTTTTTGAGACAA | 50849 |
| rs251014051 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270991 | GATATGCATAGAACT[C/T]ATACACATGCTTGCT | 50849 |
| rs251142623 | snp | A/C | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274424 | AAATGACATGGAGAT[A/C]CATAGAACTATAACT | 50849 |
| rs251224520 | in-del | -/CTTTTC | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273044 | CCTGTTCGAGGTTTC[-/CTTTTC]TTCCCGCCTCCCTAG | 50849 |
| rs251246873 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268530 | AATACCCGACCTTCC[C/G]TTAACCTCCGCCTCG | 50849 |
| rs251460165 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255866 | TACATCTAATGACTC[A/G]GCAAAGGGGAAGGGA | 50849 |
| rs251563372 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270033 | GTACAGGTGGAAGGG[C/T]GTGAAGTCAGGTCTT | 50849 |
| rs251603946 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256777 | ATCCATGACCTCCTC[G/T]CAGTCCACTCAACAG | 50849 |
| rs251605105 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243854 | TTCTCAACTACTTCC[A/G]TGAGCTCTGTCCTGA | 50849 |
| rs251715347 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115259738 | ATAAGTACTTCGGCT[A/G]CTTCCTAAATCCAGC | 50849 |
| rs251722362 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258965 | AAAGGCAAATGTAAT[A/T]CATTCACTGTATAGT | 50849 |
| rs251740255 | in-del | -/GTGTGTGTGT | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115248056 | AGAGTGTGTGTGTGA[-/GTGTGTGTGT]GTGTGTGTGTGTGTG | 50849 |
| rs251888956 | snp | C/T | | | missense | Rnf10 | GRCm38.p3 | 5:115249002 | TCATCTCAGGACCAA[C/T]AGTCCCCTCTCCCAG | 50849 |
| rs251956796 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261089 | ATATCCCTAGTCCTC[A/G]GCCAGGCACGGGGCT | 50849 |
| rs251957071 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115248315 | AGCACTTCTGAGGTG[A/G]AGGTAGGAGGATCAG | 50849 |
| rs252011615 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115265340 | CACTAAAAGAAACAC[A/G]CCCGTAAAGAAAACA | 50849 |
| rs252031980 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115247477 | CTAACAGAACAGCCT[A/G]AAGCCGACCACTATC | 50849 |
| rs252062213 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274472 | CTAGAGAGATGGCTC[A/G]GAGGTTAAGAGCACT | 50849 |
| rs252402275 | in-del | -/ACACACACACACACAC | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115263989 | CTGACTTACACTTAT[-/ACACACACACACACAC]ACACACACACACACA | 50849 |
| rs252453529 | in-del | -/TTT | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273014 | TGTGCCTGCCAATGC[-/TTT]TTTTTTTCTCTCTTC | 50849 |
| rs252483118 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250282 | CAGAAGACATCCCAG[C/T]CGCACCGCATGTTTA | 50849 |
| rs252552267 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115242219 | AGCATGCACATGGTA[C/T]ACACACATAATAAAA | 50849 |
| rs252596505 | in-del | -/GCATCT | | | intron-variant | Rnf10 | Mm_Celera | 5:115257314 | GGAGACGCTCCCCTA[-/GCATCT]GCATCCCGACTGTCC | 50849 |
| rs252619264 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250775 | GCAGCCAAGGGAGAA[C/G]ATGAACTTGTGATTC | 50849 |
| rs252644954 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257793 | TGTGGGTGCTGGAAA[C/T]CAAACTCAGGTCTCT | 50849 |
| rs252709985 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115242866 | GGGGCACCTAAGTAC[A/C]TCAGCCAGCTGGGTA | 50849 |
| rs252770116 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262410 | AGTGCTAGAATTACA[A/G]GTGTGCACCACTGGC | 50849 |
| rs252943228 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115249842 | AGGACAACCATTCGG[A/G]GCTGTGGCTTAGCCC | 50849 |
| rs253315960 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263980 | AGCTGCCTTCTGACT[C/T]ACACTTATACACACA | 50849 |
| rs253361292 | snp | A/G | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241270 | GATCTCCAGTTTACC[A/G]TGGCTCAGGTGCCTT | 50849 |
| rs253384495 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263985 | ccttctgacttacac[G/T]TATacacacacacac | 50849 |
| rs253403065 | in-del | -/GTG | | | intron-variant | Rnf10 | Mm_Celera | 5:115256942 | TGTCCTCCTCACAAT[-/GTG]GTCCCCCTTGCCCTC | 50849 |
| rs253417589 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264720 | GTTCCAGAACAGCCA[A/G]GACTATACATAGAAA | 50849 |
| rs253481001 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255629 | CAGGCAGACGCCCAA[A/G]TCCATAAACTATTTC | 50849 |
| rs253483446 | in-del | -/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261222 | AAAATAAAATCTGTA[-/T]TTTTTTTATTACATG | 50849 |
| rs253556603 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252154 | GCTGAGCAAGCCAGG[G/T]GAGGCAAGCCAGTAA | 50849 |
| rs253567097 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266236 | CTGCTGAGCCATCTC[A/G]CCAGCTCATAAATCC | 50849 |
| rs253623626 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252888 | GCATGAAGGGGTCAC[A/G]CAAAGCAGCTGAGGC | 50849 |
| rs253714609 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115245357 | AGCCATTTCCCTACC[A/G]TGTACTCAGTAAGTC | 50849 |
| rs253740539 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115266987 | CACGGCTTGTGTAGA[G/T]CTGGATGATCGCGGA | 50849 |
| rs253788918 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247672 | CCAAAGCCTGCTAAC[-/T]TTAAGTTTCTACCCT | 50849 |
| rs253892596 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115255504 | CCAAGACCTCATAGG[A/C]ATTACCCACCTCAGA | 50849 |
| rs254098543 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268975 | CAGCTTACAGATGCC[A/G]AGGGAGGGAGAGGCT | 50849 |
| rs254179207 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258794 | ATGGTTGTGAGCCAC[C/T]ATGTGGTTGCTGGGA | 50849 |
| rs254357137 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115266727 | GATGCTAGGACTTAA[A/C]CCTGCATTCTTTGGA | 50849 |
| rs254562674 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115257825 | TAAGAACTCTCTGTT[C/T]GGGGCTGGTGAGATG | 50849 |
| rs254648296 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258010 | TAAAAGAACCCTCTG[C/T]TCTTAACTCCTGAAC | 50849 |
| rs254729727 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115246780 | CTTCACTATCTTACT[C/T]ACCCCAGGAAGAATG | 50849 |
| rs254783520 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115243301 | GCATGCACGCACATA[A/C]TGCCTTTCGGGTGCA | 50849 |
| rs254909839 | snp | A/C | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261217 | TTATAAAAATAAAAT[A/C]TGTATTTTTTTTATT | 50849 |
| rs255078022 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262776 | TCTGCCTGAGGACCC[A/G]CATTAGGCTAGATGG | 50849 |
| rs255115300 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115248517 | GTTGCAGCCTCACTC[C/T]GATGAGGCCTACACG | 50849 |
| rs255164116 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250468 | CATGGTAGCCTTTAA[A/T]TCCAGCACTTGGGAG | 50849 |
| rs255264855 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115263264 | TGTTTGATTTCATTG[A/C]CGGTCTGGCAGACCT | 50849 |
| rs255425028 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115270826 | ACATCTTTGCACTAA[A/T]TACATCCAGTGATGT | 50849 |
| rs255510674 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258919 | TACTTTAATGTGCAA[A/G]CAAAAGAAGAAAAAG | 50849 |
| rs255589441 | in-del | -/ATG | | | intron-variant | Rnf10 | Mm_Celera | 5:115264051 | CATGTTCCTGAGCCC[-/ATG]AACCTCAGGGCTTCT | 50849 |
| rs255640325 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115271171 | TGGAGGTGCTTGAGA[A/G]GCAGAGGCAGGTGGA | 50849 |
| rs255871355 | snp | G/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274503 | GAATGCTTTTCCAGA[G/T]GTCCTAAACTCAATT | 50849 |
| rs255894512 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115258583 | TGGCTGTCCCTGCTG[A/G]ATCTGCCTCTGCAGA | 50849 |
| rs255970846 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252040 | TGCCTCCATGAGATC[C/T]AACTCTAAGGCATTT | 50849 |
| rs256243128 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115269747 | GAGCTAACTCTCTAG[A/C]CCCTGCTTCATTCAT | 50849 |
| rs256296159 | in-del | -/CT | | | intron-variant | Rnf10 | Mm_Celera | 5:115248103 | GTGTGCGTGCGCGCG[-/CT]CGCAGGCATATAAAA | 50849 |
| rs256351726 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260477 | GGTGCTCTGAGGAAG[C/T]GCCTCAGGAGGGTAG | 50849 |
| rs256383491 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259445 | TGTCATTGCCATTCT[A/T]CCTCCCCCTCTCTCC | 50849 |
| rs256386495 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115271709 | AGTTGTCAAGTACTC[-/T]TAAGCGCTTAGCCCA | 50849 |
| rs256416036 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256876 | AATGTGACAGGGGGA[A/G]GAGAAGGACACTTTC | 50849 |
| rs256513000 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115270783 | CACAAAAACACACTG[A/C]GGAATCCAAACAAAG | 50849 |
| rs256727719 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265045 | AAAAGTTAAGAGTAC[C/T]TCTCGCCCTTCCAGG | 50849 |
| rs256730684 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115270420 | AGTTTATACGGTTCA[A/G]AGGCGAGTTACACTA | 50849 |
| rs256796137 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274305 | GAAAAGAAAAGAAAA[A/G]AAGAAAGAAAGAAAA | 50849 |
| rs256802848 | snp | C/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273793 | TAAGCTACTACCTCA[C/T]CTAGCCGATGAGTGG | 50849 |
| rs256909008 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260390 | TATCTTTCAGCAAAG[C/T]TGAACTTATTAAATA | 50849 |
| rs257022492 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115264401 | TATAGTGTTTAAGAA[A/C]CATTATTAAGGCCGG | 50849 |
| rs257091384 | snp | A/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115250117 | CAGCTTGGAATACTG[A/G]CTGAGCTGCTCATCT | 50849 |
| rs257299656 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115250403 | AGGACAAACCTAGAT[A/C]ATCCAGCCATCCTAT | 50849 |
| rs257385201 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115254433 | CACACTTAAAAGACT[C/T]TTAATTGTAAAAAGA | 50849 |
| rs257408836 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264417 | CATTATTAAGGCCGG[A/G]TGTGGTGGCACACGC | 50849 |
| rs257479868 | snp | G/T | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115251360 | TGAAAGATAGTGCAG[G/T]ATGCATGCCCAGCAG | 50849 |
| rs257701616 | in-del | -/TT | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115262170 | ACAAATGGCTTCTGG[-/TT]TTACTTTACTTAGAT | 50849 |
| rs257800904 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258361 | CACTCCCACTCCTCT[C/T]GAACGTCCGTCTGTC | 50849 |
| rs257807036 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259977 | ATGTCTCCTCCCCCA[G/T]GGGTGTCACAGACCC | 50849 |
| rs257839145 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115267676 | GGAGGTTGAGGACAG[A/G]AGAATACAGATGAGA | 50849 |
| rs257855883 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258485 | TCCCGCTTACTCGCT[C/T]GCCTCAAACCCCAGC | 50849 |
| rs257878610 | snp | A/G | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241570 | ACTCCAGTTGCAGGG[A/G]CCAACAGACAGGCAT | 50849 |
| rs257941098 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247103 | CCGTGCGTGTCTCAG[C/T]ATACAGCTCAAGCCC | 50849 |
| rs258275633 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245209 | AAGGACTCTTAATTC[C/T]GTCGGGAGAAGGTCT | 50849 |
| rs258303749 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263894 | AGAGGACCAACATGC[C/T]AGAGTGACTGCTACC | 50849 |
| rs258464031 | snp | C/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241693 | TCCCAGGAGAAAAAC[C/T]TGCAGCAGAGCAGTG | 50849 |
| rs258914423 | snp | A/G | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241532 | CAGCTCCTACACGGA[A/G]GCTCACAATCAAATG | 50849 |
| rs258915529 | in-del | -/A | | | intron-variant | Rnf10 | Mm_Celera | 5:115248270 | ATTACAATAAGTTTT[-/A]AAAAAACAAACAAAC | 50849 |
| rs258993293 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115244617 | CTCCAAGCTGAGATG[G/T]TTGCTGTGGACTGGT | 50849 |
| rs259083083 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115251647 | TGTCCCCGATTTGGT[-/G]GGACTGTTTGAAAAG | 50849 |
| rs259174601 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115249894 | CAACATGCCCTCCTT[C/T]CCATTCCCACCTAAC | 50849 |
| rs259264656 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115269437 | AGTTTCTTTCTTTTC[A/T]CTCTTCTTAGTTTTT | 50849 |
| rs259822498 | snp | A/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273194 | TTTTTTTCTTTTTTT[A/T]AAAAAAAGATGTGTG | 50849 |
| rs259914524 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243109 | TGCATAGCCCAGGCT[-/G]ACCAGGAACTCACTC | 50849 |
| rs259956606 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243731 | ATTCCCCATCCTCTG[C/T]TCACCACTCAAATGC | 50849 |
| rs260031230 | in-del | -/CT | | | intron-variant | Rnf10 | Mm_Celera | 5:115243122 | GCTACCAGGAACTCA[-/CT]CTGTGGACCAGACTG | 50849 |
| rs260053830 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262929 | TAAAGTGGAGACGCT[A/G]GAGAGAGTCTCCCGC | 50849 |
| rs260112379 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115270437 | GGCGAGTTACACTAA[-/C]ACCTGCTTAGACAGT | 50849 |
| rs260150792 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242626 | CCTTGCCGTCTGACC[A/G]CTCTCACCTTTCTTT | 50849 |
| rs260182401 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115260731 | AGGACAGCCAAGACA[A/G]AGAGACATTCTGTCA | 50849 |
| rs260291921 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115248746 | CTATCACACAAGCCC[A/C]GGCCAGCCTCCAGCA | 50849 |
| rs260293571 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261339 | GTCCTGCCAATGTGC[A/G]GGGTCTGGAAAAAAA | 50849 |
| rs260373911 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115246033 | GCAATGGAGGTCCAT[A/G]TACACAGCTGGTCAG | 50849 |
| rs260437598 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274784 | ATTAAAGCACCATAT[A/G]GGCTCTGGGAATCAA | 50849 |
| rs260515257 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265175 | AGGTCTGGGCTTGAT[C/T]ATCAGCACACCATAA | 50849 |
| rs260523870 | in-del | -/GG | | | upstream-variant-2KB | Rnf10 | GRCm38.p3 | 5:115273714 | GGACGAATGGAATTT[-/GG]GGGGGGGGGGCTGTT | 50849 |
| rs260534895 | in-del | -/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115251046 | TCATTAAGGGTCAGT[-/C]CCCCCCCCCTCGTGC | 50849 |
| rs260589684 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256098 | CTGCTGTAACTGCAG[C/T]TCGCAGGGAACTGCA | 50849 |
| rs260617460 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115255145 | ACCACATGGTGGCTC[A/C]CAACCATCCGTAATG | 50849 |
| rs260629589 | in-del | -/CTCACACACACACACACACACACA | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271602 | CATCACTCTCTCTCT[-/CTCACACACACACACACACACACA]CACACACACACACAC | 50849 |
| rs260652827 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115265909 | CAAGCCCAAGCCAAT[C/T]CTTTGAAAGCACAGG | 50849 |
| rs260891550 | snp | A/G | | | synonymous-codon | Rnf10 | Mm_Celera | 5:115242020 | AGGTGCTGAACAGCA[A/G]CTTCTGCTTCTGTCT | 50849 |
| rs260997842 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115262615 | TGGGATTAAAGGCGT[-/G]CGCCACTAACATCCA | 50849 |
| rs261007991 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273931 | CTCAGCACTCAGGAG[A/G]CAGATGCAGGTGGAT | 50849 |
| rs261305063 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115257609 | CCTTGGCTACAGTCA[C/G]GACTACACAGAAAAA | 50849 |
| rs261685757 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115256078 | TCATGCCAGGGGGCT[A/T]CCAGCTGCTGTAACT | 50849 |
| rs261712968 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115262506 | CAAATCACTAATAAG[-/T]TTTTTTTTTTCCCTT | 50849 |
| rs261713655 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115247531 | AGAACAGGGAGAGAG[A/G]ACTTGCTGACACCAA | 50849 |
| rs261793183 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115245662 | TTCTTGCAGACTGAC[C/T]TGAGTTTGGTTCCCA | 50849 |
| rs261864544 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261192 | GACTGTGAATTCCAG[A/G]ACAACTTCATTATAA | 50849 |
| rs261973473 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115255085 | TGGCTCAGCGGGTAA[A/G]AGCACTGACTGCTCT | 50849 |
| rs262056916 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115243152 | TGGCTTCAAGATCAC[A/T]AAAATCTGTCTGGTT | 50849 |
| rs262238693 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115263912 | AGTGACTGCTACCAA[A/G]TCTGAGTTCAAGTCC | 50849 |
| rs262431904 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115269010 | CATGGTGGTGACACA[C/T]ACCTACAGCTCCAAC | 50849 |
| rs262477446 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258859 | CTCTTAACTGCTGAG[C/T]CTTCTCTCCAGCCCC | 50849 |
| rs262480242 | in-del | -/TT | | | intron-variant | Rnf10 | Mm_Celera | 5:115246626 | CTCTCTCCCTCCCTC[-/TT]TCCCTCTCCCTTTCC | 50849 |
| rs262505894 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115262914 | ACAGTCTCAAAAAAA[C/T]AAAGTGGAGACGCTA | 50849 |
| rs262589011 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250319 | AGAACATAATGTTAG[C/T]CCATAGGTCTAGCCA | 50849 |
| rs262634147 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115250674 | AAGGGTCGTGGGTGA[-/T]TTTATGTCCTCATTG | 50849 |
| rs262653207 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266078 | AGAGAGACAGACAGA[A/G]ATAGAGACACACCAC | 50849 |
| rs262709812 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115256187 | GCAATTTAATTCTTT[A/G]GAAAAACGGAGTGCC | 50849 |
| rs262799209 | in-del | -/TCA | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273846 | GAGAACTAGAGTGGC[-/TCA]TCATGCCTGTATCAC | 50849 |
| rs262921745 | snp | A/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274103 | AGACCATGTTCCTTA[A/T]AAGAGAGAAAAAGAA | 50849 |
| rs262949328 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115262612 | TGCTGGGATTAAAGG[C/T]GTGCGCCACTAACAT | 50849 |
| rs262949646 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258679 | CCACCAGCACTGGCT[C/T]CTCTTTAACCTGCCG | 50849 |
| rs263170658 | in-del | -/CC | | | intron-variant | Rnf10 | Mm_Celera | 5:115270880 | TGCTCTTCCAGGAGA[-/CC]CCCCCTCTCCCACTC | 50849 |
| rs263210816 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264166 | TAGTGCTACCTCTGC[C/T]GATTCGTGTCTGCTA | 50849 |
| rs263211776 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115270360 | CTCTCTCCAACAACA[A/G]CCAAGATTTACAATA | 50849 |
| rs263244756 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242369 | AAGCCTGAGCTCTGA[A/G]TTGAGTGAGTTTCCC | 50849 |
| rs263364719 | in-del | -/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115259922 | CTCCAGAGGGCACAT[-/G]AAGTGTGAAGTGACA | 50849 |
| rs263549073 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115262867 | AACAGCCAGTTTAGT[C/T]AAAAAGGCAACTTCC | 50849 |
| rs263593815 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115272243 | AGTGACCCGGCAGAC[C/T]CGCCGGCTCTTACCA | 50849 |
| rs263702249 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115255185 | ACGTACTCTTCAGAG[A/T]CAGCTACAGTGTACT | 50849 |
| rs263737019 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269924 | GAAAAATAGATTAAA[A/G]AAAAGGTCAGTCAGG | 50849 |
| rs263750342 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115271155 | GCTGTGTCTGAGATT[C/T]TGGAGGTGCTTGAGA | 50849 |
| rs263886492 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115245097 | CATGGTCTAGCCCCC[A/G]TTCCTGCCACTGAAG | 50849 |
| rs263967668 | snp | A/T | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115274448 | TATAACTTGGGGGGG[A/T]GGGGTTTGCTAGAGA | 50849 |
| rs263987218 | in-del | -/ACACACACACAC | | | intron-variant | Rnf10 | Mm_Celera | 5:115264973 | ATATGACACATACAA[-/ACACACACACAC]ACACACACACACACA | 50849 |
| rs264108400 | in-del | -/GTA | | | intron-variant | Rnf10 | Mm_Celera | 5:115263771 | ATAAAGAAATGGTCT[-/GTA]GTTGTTGTAGGAAGG | 50849 |
| rs264158291 | snp | A/G | | | downstream-variant-500B | Rnf10, Pop5 | Mm_Celera | 5:115241451 | TGCCTCCTGCCTGTC[A/G]GATGGTTTACAACTG | 50849 |
| rs264249260 | in-del | -/ACAT | | | intron-variant | Rnf10 | Mm_Celera | 5:115264759 | CAAACAAACAAACAA[-/ACAT]ACATGTCTACATGCA | 50849 |
| rs264293939 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115264327 | TGTAAACAGGTCCTC[-/T]TTTCCCCCTATTCTT | 50849 |
| rs264340861 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273446 | TGGAGAGTCTTGGAG[A/G]AAAACACTCAATGGC | 50849 |
| rs264402964 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115243003 | GGCATAGAGACCTTA[A/C]GGATATACTGTGTCT | 50849 |
| rs264596042 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115258372 | CTCTCGAACGTCCGT[C/T]TGTCCGTCTGTCCGC | 50849 |
| rs264626299 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115242374 | TGAGCTCTGAGTTGA[A/G]TGAGTTTCCCGCCCT | 50849 |
| rs264826588 | in-del | -/A | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115270560 | TCATACCCTACAGAT[-/A]AAACTCTCAGTCAGT | 50849 |
| rs264847067 | snp | C/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115251614 | AAGAACACTTCCGCC[C/T]GTGCAGTCTGAATGA | 50849 |
| rs264857038 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264194 | CTAGCTCAACTCTAC[A/G]GAACTGGACCACTGG | 50849 |
| rs264895796 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115243898 | CACTGTGCATGTGGT[A/G]ATGATGTGGGTGATG | 50849 |
| rs264981301 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115259147 | CTGAGTTCAAGGTCA[A/T]CCTGTTCTACAGAGT | 50849 |
| rs265110739 | snp | C/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261435 | AAATTCAATGGAGCA[C/G]ACAATGGAGTTCAGA | 50849 |
| rs265242263 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115266783 | TCTCTCCAGCCTCAG[A/G]ATAAAAAAGAAAAGA | 50849 |
| rs265383802 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115269598 | TTTTATGTGTATGGT[A/G]CTTTGCTTGCAAGTT | 50849 |
| rs265473046 | snp | A/G | | | intron-variant, upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115261151 | GCCAGGAGAACTGCC[A/G]ACGAACTTAAGATCA | 50849 |
| rs265490321 | snp | G/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263152 | GCTGACTATGAGTCT[G/T]TGAATGAGTGCATAG | 50849 |
| rs265507523 | snp | C/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115272929 | CTATTTATATAGTTG[C/G]CAGGCGGGCGTGGTG | 50849 |
| rs265618977 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115268328 | CACACAATCATCTGT[A/G]ACTGTACAGGAATTC | 50849 |
| rs265663318 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115253003 | CAGTGTTTTGGAGAT[A/G]CCAGTACCATGAGAT | 50849 |
| rs265711194 | in-del | -/TTTTT | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115270595 | TTATAATTTTAGTGC[-/TTTTT]TTTTTTTTTTTTTTT | 50849 |
| rs265874282 | snp | A/G | | | upstream-variant-2KB | Rnf10 | Mm_Celera | 5:115273746 | AGGGATCAAATCCAG[A/G]GCTCCATGCTCACAA | 50849 |
| rs265908358 | snp | A/C | | | intron-variant | Rnf10 | Mm_Celera | 5:115243320 | CTTTCGGGTGCAGTC[A/C]TAAGCCGTGGCCCAG | 50849 |
| rs266178085 | snp | A/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115250357 | ATGCTCAGGAAGATG[A/G]TCTCCTAAGAATGAA | 50849 |
| rs266210095 | snp | C/T | | | downstream-variant-500B | Rnf10 | Mm_Celera | 5:115241674 | ATCAACAGGCACAGC[C/T]TCTTCCCAGGAGAAA | 50849 |
| rs386864833 | in-del | -/GGTACGCACACAT | | | intron-variant | Rnf10 | Mm_Celera | 5:115242227 | ATGGTACACACACAT[-/GGTACGCACACAT]AATAAAAAAGAGTTC | 50849 |
| rs386879366 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115254955 | CTTTCCTCCCCAACT[-/T]GCTTCTTGGTCATGA | 50849 |
| rs386939402 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254911 | CCTTGGAGATGAACA[A/G]CAGTATGGAAGTGTA | 50849 |
| rs387001763 | in-del | -/GG | | | upstream-variant-2KB | Rnf10 | GRCm38.p3 | 5:115273725 | AATTTGGGGGGGGGG[-/GG]CTGTTAGGGATCAAA | 50849 |
| rs387035938 | snp | C/G | | | intron-variant | Rnf10 | Mm_Celera | 5:115264413 | GAAACATTATTAAGG[C/G]CGGGTGTGGTGGCAC | 50849 |
| rs387095240 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263785 | TGTAGTTGTTGTAGG[A/T]AGGAAGGAAGGAAGG | 50849 |
| rs387116511 | in-del | -/TTTT | | | intron-variant | Rnf10 | Mm_Celera | 5:115270609 | GCTTTTTTTTTTTTT[-/TTTT]GCTCTTTAATTTGAG | 50849 |
| rs387242047 | in-del | -/ACACACACAC | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115263989 | CTGACTTACACTTAT[-/ACACACACAC]ACACACACACACACA | 50849 |
| rs387269303 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115247674 | AAAGCCTGCTAACTT[-/T]AAGTTTCTACCCTTT | 50849 |
| rs387280675 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263789 | GTTGTTGTAGGAAGG[A/T]AGGAAGGAAGGAAGG | 50849 |
| rs387302682 | in-del | -/TCACACACACAC | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271603 | ATCACTCTCTCTCTC[-/TCACACACACAC]ACACACACACACACA | 50849 |
| rs387364478 | in-del | -/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254954 | CCTTTCCTCCCCAAC[-/T]TGCTTCTTGGTCATG | 50849 |
| rs387384448 | in-del | -/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263592 | TACTTTCATTTTTTT[-/T]ACTTAAACATTTTTA | 50849 |
| rs387507335 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254797 | TCTATAAGAGAGCAG[A/G]CTGAGCAAGCCAGGG | 50849 |
| rs387532991 | in-del | -/AGGAGGAGG | | | cds-indel | Rnf10 | Mm_Celera | 5:115272652 | ACGAGGAGGAGGAGG[-/AGGAGGAGG]CCGGGGCTCGGAGGT | 50849 |
| rs387607235 | in-del | -/TGA | | | intron-variant | Rnf10 | Mm_Celera | 5:115264052 | ATGTTCCTGAGCCCA[-/TGA]ACCTCAGGGCTTCTC | 50849 |
| rs387613486 | in-del | -/AGGAAGGA | | | intron-variant | Rnf10 | Mm_Celera | 5:115263782 | GTCTGTAGTTGTTGT[-/AGGAAGGA]AGGAAGGAAGGAAGG | 50849 |
| rs387646144 | snp | A/T | | | intron-variant | Rnf10 | Mm_Celera | 5:115263793 | TTGTAGGAAGGAAGG[A/T]AGGAAGGAAGGAAGG | 50849 |
| rs387666292 | in-del | -/AGAG | | | intron-variant | Rnf10 | Mm_Celera | 5:115248052 | GTGAGAGTGTGTGTG[-/AGAG]TGAGTGTGTGTGTGT | 50849 |
| rs387693219 | in-del | -/AC | | | intron-variant | Rnf10 | Mm_Celera | 5:115264029 | CACACACACACACAC[-/AC]CATGGCATGTTCCTG | 50849 |
| rs387725645 | in-del | -/GTTTTGTGTCAACTTGACACAGCTGGAGTTATCACAGAGAAAGGACCTTCAGTTGAGGAAATGCCTTGTATTGGCTA | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115251887 | CACCTGTACTGGTTG[lengthTooLong]GTTTTGTGTCAACTT | 50849 |
| rs387816831 | in-del | -/CTCAAATGATAATTTTTTTTTTTTTTTTTTAAAGATTTATTTATTTATTTATTATATGTAAGTACACTGTAGTTGTCTTCAGACACTCCAGAAGAGGGAGTCAGATCTTGTTACAGATGGCTGTGAGCCACCATGTGGTTGCTGGGATTTGAACTCTGGACCTTCGGAAGAACAGTCGGGTGCTCTTACCCACTGAGCCATCTCACCAGCC | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115267924 | CAATCCCAGCTAATG[lengthTooLong]CTCAAATGATAATTT | 50849 |
| rs578545536 | snp | C/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252105 | TGGGTGGGACCATCT[C/G]TGGGCTGGTAGTCTT | 50849 |
| rs578629904 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115251963 | TGCCTTGTATTGGCT[A/G]GTTTTGTGTCAACTT | 50849 |
| rs578651347 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265809 | TACTGTTTTAAAAGA[A/G]GTAAGCACTTTTTTT | 50849 |
| rs578756594 | snp | A/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115246663 | TCTCTCTCTCTCACG[A/C]CCAGATCCTGAATGT | 50849 |
| rs578838626 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115256327 | CAAAAGAGGGCATCA[A/G]ATGCCCTGGACCTAA | 50849 |
| rs579098653 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115242905 | GCTTCACACCAAGAA[C/T]CACAGAATTGGGGAG | 50849 |
| rs579199716 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115255166 | ATCCGTAATGAGATC[C/T]GACACGTACTCTTCA | 50849 |
| rs579256076 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115246684 | TCCTGAATGTGCCCC[C/T]GCCCTCCTGTGAGCA | 50849 |
| rs579326504 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265465 | CAGAGTGAGTTTCAG[A/G]ACAGCCAGGGCTACA | 50849 |
| rs579355436 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252139 | TCTATAAGAAAGCAG[A/G]CTGAGCAAGCCAGGT | 50849 |
| rs579456337 | snp | A/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254663 | AGTTATCACAGAGAA[A/C]GGAGCTTCAGTTGGG | 50849 |
| rs579465404 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115267171 | CACATAAGGATTTAT[A/G]ATTTCAGGCAAAAAA | 50849 |
| rs579790701 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271607 | ACTCTCTCTCTCACA[C/T]ACACACACACACACA | 50849 |
| rs579912546 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254294 | GTTGTGTAGGAGCTT[G/T]GAAGATAATGTTGAG | 50849 |
| rs579961316 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115248098 | TGTGTGTGTGCGTGC[A/G]CGCGCTCGCAGGCAT | 50849 |
| rs580003698 | snp | A/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115257554 | CCCCCTCCCCCCAGC[A/C]TTGGAACACACAGGC | 50849 |
| rs580057354 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115263332 | CAGCTGTATAACAAA[G/T]ACTGGATCAAAGAGA | 50849 |
| rs580540869 | snp | A/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115269095 | ACTGTCTCCAGAAAC[A/C]AAACACATTTTGTGT | 50849 |
| rs580656697 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265445 | TTCGAGGCCAGCCTG[A/G]TCTACAGAGTGAGTT | 50849 |
| rs581053575 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254709 | CATCCAGCTGTAAGG[C/T]ATTTTCTCAATTAGT | 50849 |
| rs581130713 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115251957 | AGGAAATGCCTTGTA[C/T]TGGCTAGTTTTGTGT | 50849 |
| rs581169543 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115251986 | GTCAACTTGACACAG[C/T]TGGAGTTATCACAGA | 50849 |
| rs581679377 | snp | C/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254694 | GAAATGCCTCCAGGA[C/G]ATCCAGCTGTAAGGT | 50849 |
| rs581689890 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115250581 | CAAAACAAAATCCAC[C/T]AACAGACGTGAGCCA | 50849 |
| rs581720060 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115257555 | CCCCTCCCCCCAGCA[C/T]TGGAACACACAGGCA | 50849 |
| rs581805575 | snp | C/G | | | upstream-variant-2KB | Rnf10 | GRCm38.p3 | 5:115274645 | ATTTTTAAAAAGGAA[C/G]TATAATTTTTCAGTT | 50849 |
| rs581810298 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115267622 | GGGTCACTTCCAGGG[C/T]TTTAAGATTATGAAT | 50849 |
| rs581873101 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115246677 | GCCCAGATCCTGAAT[G/T]TGCCCCTGCCCTCCT | 50849 |
| rs581969298 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252106 | GGGTGGGACCATCTC[G/T]GGGCTGGTAGTCTTG | 50849 |
| rs582270797 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115253054 | GCAGTGGAGTACAGG[C/T]ATCTGGAGCCTAGAG | 50849 |
| rs582317992 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115266076 | TGAGAGAGACAGACA[A/G]AGATAGAGACACACC | 50849 |
| rs582482504 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265686 | TTTTCGTGTGTATAC[C/T]AATCTCTGTGTCCGT | 50849 |
| rs582585858 | snp | A/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115256574 | AAGTCCAAGCCTAAG[A/C]AACACCTGTGAGAGC | 50849 |
| rs582891935 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115255509 | ACCTCATAGGAATTA[C/T]CCACCTCAGAGTTCA | 50849 |
| rs582974225 | snp | A/C | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115246687 | TGAATGTGCCCCTGC[A/C]CTCCTGTGAGCAGGT | 50849 |
| rs582976418 | snp | A/C | | | upstream-variant-2KB | Rnf10 | GRCm38.p3 | 5:115273571 | CATTCGAAACACCAA[A/C]AAAGAGAAACAACAT | 50849 |
| rs583190703 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254677 | AAGGAGCTTCAGTTG[A/G]GGAAATGCCTCCAGG | 50849 |
| rs583229636 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271637 | ACACACACACACACC[A/G]TGAAAGCCAAGCCCA | 50849 |
| rs583436458 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254698 | TGCCTCCAGGACATC[C/T]AGCTGTAAGGTATTT | 50849 |
| rs583571283 | snp | C/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254309 | TGAAGATAATGTTGA[C/G]AACAGTGCAGAAAAT | 50849 |
| rs583701404 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115248112 | CGCGCGCTCGCAGGC[A/G]TATAAAACAAGAACA | 50849 |
| rs583702882 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115269110 | CAAACACATTTTGTG[G/T]GTTTTTCTTTGTGTT | 50849 |
| rs583819611 | snp | C/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115263447 | ACAGGTACATACAGC[C/G]TGCTGTAGTGAACCT | 50849 |
| rs583887798 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115250667 | GTTTAGGGAAGGGTC[A/G]TGGGTGATTTATGTC | 50849 |
| rs584007527 | snp | C/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115264450 | TTAATCCCAGCACTC[C/G]GGAGGCAGAGGCAGG | 50849 |
| rs584088212 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115258853 | TCAGTGCTCTTAACT[A/G]CTGAGCCTTCTCTCC | 50849 |
| rs584202854 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115246636 | CCCTCTTTCCCTCTC[C/T]CTTTCCCTCTCTCTC | 50849 |
| rs584317795 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254947 | AATAAACCCTTTCCT[C/T]CCCAACTTGCTTCTT | 50849 |
| rs584324736 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252019 | AAGGAGCTTCAGTTG[A/G]GGAAATGCCTCCATG | 50849 |
| rs584584211 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115255511 | CTCATAGGAATTACC[C/T]ACCTCAGAGTTCAGA | 50849 |
| rs584892402 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115242239 | ACATAATAAAAAAGA[A/G]TTCCTCACAAGTCCA | 50849 |
| rs584896752 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115251961 | AATGCCTTGTATTGG[C/T]TAGTTTTGTGTCAAC | 50849 |
| rs584948406 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115252133 | CTTGGTTCTATAAGA[A/G]AGCAGGCTGAGCAAG | 50849 |
| rs585002608 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265769 | AACCTCACCCTCAAA[A/G]ATTGTGCCTCTCATA | 50849 |
| rs585011954 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115265452 | CCAGCCTGGTCTACA[A/G]AGTGAGTTTCAGGAC | 50849 |
| rs585143189 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115266519 | AGCCACTGTTGAGCA[C/T]AGCGCAGCGCCACTG | 50849 |
| rs585335268 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115248116 | CGCTCGCAGGCATAT[A/G]AAACAAGAACAAATT | 50849 |
| rs585541266 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115258852 | GTCAGTGCTCTTAAC[C/T]GCTGAGCCTTCTCTC | 50849 |
| rs585653868 | snp | C/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115246680 | CAGATCCTGAATGTG[C/G]CCCTGCCCTCCTGTG | 50849 |
| rs585793911 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254484 | TGGATATTTTAAAAG[A/G]ATTGAACTTTTAATA | 50849 |
| rs586124851 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254024 | GCTCCTGCTTCCTGA[C/T]CTGCTTGAGTTCCAG | 50849 |
| rs586149000 | snp | A/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115248053 | GTGAGAGTGTGTGTG[A/T]GAGTGTGTGTGTGTG | 50849 |
| rs586569975 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271721 | ACTCTAAGCGCTTAG[C/T]CCATTTACTTAATAG | 50849 |
| rs586771150 | snp | A/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115257251 | GCTCCGCTTCCTTCC[A/T]CATGGCTGAGAACTG | 50849 |
| rs586775299 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115264633 | CAGGGCATATATATA[G/T]ATAGATATAGATATA | 50849 |
| rs587025000 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254691 | GGGGAAATGCCTCCA[G/T]GACATCCAGCTGTAA | 50849 |
| rs587095587 | snp | G/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254877 | GCTTTCTTACCTGCT[G/T]GAGTTCCAGTCCTGA | 50849 |
| rs587332465 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115254700 | CCTCCAGGACATCCA[A/G]CTGTAAGGTATTTTC | 50849 |
| rs587374834 | snp | A/T | | | upstream-variant-2KB | Rnf10 | GRCm38.p3 | 5:115274636 | AATAAATCCATTTTT[A/T]AAAAGGAACTATAAT | 50849 |
| rs587421518 | snp | A/G | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115271528 | AAGTAGTATTATTAT[A/G]TTATTATAATAATAT | 50849 |
| rs587485157 | snp | C/T | | | intron-variant | Rnf10 | GRCm38.p3 | 5:115251043 | CTGTTCATTAAGGGT[C/T]AGTCCCCCCCCCTCG | 50849 |
| rs587557147 | snp | C/T | | | intron-variant, upstream-variant-2KB | Rnf10 | GRCm38.p3 | 5:115261596 | CACAAATAAATAATA[C/T]ATAAATATGAGTCTG | 50849 |