| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs13466800 | snp | C/T | | | synonymous-codon | Rnf187 | Mm_Celera | 11:58938784 | CCGCCGCCCGCAGCC[C/T]TGGCGCTCCCCGCGG | 108660 |
| rs13466801 | snp | C/T | | | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58938647 | CGAGGAGGACGGGCC[C/T]TTCCCGTGCCCGGAG | 108660 |
| rs13466802 | snp | A/G | | | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58933054 | ACCACTTGGCAGCTC[A/G]GAAGCCCCTGCTTCT | 108660 |
| rs13466803 | snp | C/T | | | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58938494 | GCTGCAGCTGCTCTG[C/T]CGCGCCGACGGGGAT | 108660 |
| rs13466804 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58934069 | CGCTTCCGGTCCCTG[C/T]TGCAGGCTGTGTCAG | 108660 |
| rs13466805 | snp | A/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933069 | CCAGCCCTGCCTGGG[A/T]CCACTTGGCAGCTCG | 108660 |
| rs13466806 | snp | C/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58932676 | ATCCCCAAAGTGATT[C/T]CTCCTCCTTCCCACC | 108660 |
| rs13466807 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932836 | GGGTTTGGCTGGGAC[C/T]TGAGTGTTAATGCAG | 108660 |
| rs13466808 | snp | A/G | 0.408163 | 0.193609 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932958 | TTCCCATTGGTGCCC[A/G]TGACAGGGTTGGCTC | 108660 |
| rs26971820 | snp | G/T | 0.5 | 0 | synonymous-codon | Rnf187 | GRCm38.p3 | 11:58934034 | GCTGAGGCCCAGGTT[G/T]CGGTGCTTCTTCTCC | 108660 |
| rs26971821 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Rnf187 | Mm_Celera | 11:58933527 | ACAGAGCCAAGGTGA[C/T]TTGACAACCCATCTA | 108660 |
| rs26971822 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf187 | Mm_Celera | 11:58933500 | AGTGCTGCTATCCTG[A/C]GTACAATGCACACAG | 108660 |
| rs29386458 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936773 | TAAAAGGGACTCCCA[A/C]AGAGCCCCCTCCCCA | 108660 |
| rs29388353 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932896 | ACTAACACACACAGG[C/T]TGACTGTAACTGGTG | 108660 |
| rs29394203 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940221 | TAAATAAATAAATAA[A/T]TAAATAAAAGTGTGT | 108660 |
| rs29394747 | snp | A/G | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935856 | ACCAGACACACTCTC[A/G]TTTCTGAGTACATTT | 108660 |
| rs29397346 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939145 | CCAAACCCAGATCCT[C/T]ACAAAGATACTCCCT | 108660 |
| rs29402991 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939612 | GTGTGTCACTGTGGC[C/T]GTGGGCTTTGAGACC | 108660 |
| rs29406824 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937435 | GGATTTTAGGTAGGT[C/T]CCCTTTAGTGTCAGC | 108660 |
| rs29409297 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935836 | GCTGGACAAGCACTG[C/T]ACCAACCAGACACAC | 108660 |
| rs29410563 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939316 | GCAGGATAAAACTGG[C/T]TAGGTAGGCAGATGC | 108660 |
| rs29412533 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940213 | TAAATAAATAAATAA[A/T]TAAATAAATAAATAA | 108660 |
| rs29414988 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939883 | GCTCCAAACACTATG[A/G]CAGCAGCCACATCTG | 108660 |
| rs29416275 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937556 | GGACAACCCCAGCAG[C/T]ATGTTCTGACAGAGT | 108660 |
| rs29421098 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935789 | TGTCTGTGGTGCTTG[C/T]TTTGCACGATTACAT | 108660 |
| rs29421151 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936899 | AATCATGTGTGTGGT[A/T]TTGTGTGGCAGCCAG | 108660 |
| rs29433997 | snp | A/G | 0.5 | 0 | intron-variant | Rnf187 | Mm_Celera | 11:58936235 | TGCCAGCCAGATAAC[A/G]GCTGTCTGGCCAAGC | 108660 |
| rs29434418 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936822 | AGTGAGAAAGGCCAC[A/C]GGAAGCTAGCCCCAA | 108660 |
| rs29438000 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939787 | GCCCCAGTTAAATGT[C/T]CTTTATAAGAGTTAC | 108660 |
| rs29440469 | snp | C/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939463 | ATTGTGTTAATACAG[C/G]TGTAGTCAGCTATCT | 108660 |
| rs29442033 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936924 | AGCCAGAAAACAGAA[G/T]GTTCTACTGGTAACA | 108660 |
| rs29442154 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf187 | Mm_Celera | 11:58936649 | CTAGCTAAGTACCAA[A/C]TCTGTGTGTCCCCAA | 108660 |
| rs29445525 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf187 | Mm_Celera | 11:58936107 | ACCTTGACAGCAGGA[C/T]TGGAAACAGACACTC | 108660 |
| rs29447736 | snp | G/T | 0.32 | 0.24 | intron-variant | Rnf187 | Mm_Celera | 11:58937342 | GAAAGTGGTTGTTTC[G/T]TAAAAGGGTCTCCTG | 108660 |
| rs29449002 | snp | A/G | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58938179 | AATAGCTCGAGGGAC[A/G]TAGCAGGGTCCGGGA | 108660 |
| rs29451560 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf187 | Mm_Celera | 11:58936268 | CCTCTGACTACAGGA[C/T]CCCCATCTTCGTATT | 108660 |
| rs29455279 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937514 | TTTGTGGAGATTGCT[C/G]TCTTAGTAAGGGGAC | 108660 |
| rs29462159 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937593 | ACCTCAGTTTGGGAC[C/T]TGGATGTAACCACAG | 108660 |
| rs29468395 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf187 | GRCm38.p3 | 11:58936086 | AGCAACACTTCTAGC[A/G]GCCTAACCTTGACAG | 108660 |
| rs29471820 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf187 | GRCm38.p3 | 11:58937048 | AGAGAGGAGCCCTAC[A/G]GACACTCAACTCACC | 108660 |
| rs29474736 | snp | C/T | 0.5 | 0 | intron-variant | Rnf187 | GRCm38.p3 | 11:58935664 | CCCCTGTGCTGCAGG[C/T]CCTCTCCACTGGATA | 108660 |
| rs29480356 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf187 | Mm_Celera | 11:58936487 | GGGAACTATAATGAA[C/T]TTTAATATATAAAAG | 108660 |
| rs29484551 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932335 | AACCCAGCCCACCTG[C/T]GAGTCAAGTTGAGGC | 108660 |
| rs29486311 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940217 | TAAATAAATAAATAA[A/T]TAAATAAATAAAAGT | 108660 |
| rs29487085 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939804 | TTTATAAGAGTTACA[C/T]TGGTCATGGTGTCTC | 108660 |
| rs33849103 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940276 | GAAAGAGAATTGTGT[A/G]TGTGTGTGTGTGTGT | 108660 |
| rs45760476 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935239 | CTATGAAACGGCACA[A/G]CATTAACACAGATGC | 108660 |
| rs45948376 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940009 | TCTAGGAAAAAAATA[C/T]TACATAGAAAGATGC | 108660 |
| rs45982749 | snp | G/T | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940893 | AGCTTTAAGATTAGT[G/T]GCCCTTATCAGAATT | 108660 |
| rs46013744 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935646 | CAGAGCCACCTGCAT[C/T]CCCCCCTGTGCTGCA | 108660 |
| rs46076054 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935667 | CTGTGCTGCAGGTCC[A/T]CTCCACTGGATACAA | 108660 |
| rs46693454 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933730 | GGATGAGGGATGACA[G/T]GGGGGATACCCTGGC | 108660 |
| rs46713005 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58935305 | TCTAACACAGAGCCA[C/T]CTGCATCCTCTCCTT | 108660 |
| rs46821867 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940018 | AAAATATTACATAGA[A/G]AGATGCATGTAAATA | 108660 |
| rs46822979 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935431 | CCTGTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs46838563 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933602 | ACAGCTGATGGGTAT[A/G]TGGGAAGGGAATACC | 108660 |
| rs46908253 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935399 | TCTAACACAGAGCCA[C/T]CTGCATCCTCTCCTT | 108660 |
| rs47036666 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934374 | AATTAAATCTACTTT[A/T]AAAACTAAAATCACA | 108660 |
| rs47037929 | snp | C/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933211 | TATGTGCATGGCCAG[C/T]GGGGCACCTCTGATG | 108660 |
| rs47043427 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934632 | ACCACCTTGGGTGCA[A/T]TCACTAGACACAGTA | 108660 |
| rs47169723 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933743 | CAGGGGGGATACCCT[A/G]GCTACTCCTGCTCAC | 108660 |
| rs47449036 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934949 | TCGAACTCAGAAATC[C/T]TCCTGCCTCTGCCTC | 108660 |
| rs47604724 | snp | A/C | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940011 | TAGGAAAAAAATATT[A/C]CATAGAAAGATGCAT | 108660 |
| rs47778021 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934643 | TGCATTCACTAGACA[C/T]AGTAGGCAGAGCCTT | 108660 |
| rs47982461 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933665 | AAGCTCAGGCTGACT[G/T]CCAAGCAGGTTGCCT | 108660 |
| rs48899298 | snp | A/G | | | utr-variant-3-prime | Rnf187 | GRCm38.p3 | 11:58932645 | TTCTGCAGGGAAGGA[A/G]GTCCCTTCCATCAGA | 108660 |
| rs49285351 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935383 | TCCCTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs49330478 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933597 | CCCAAACAGCTGATG[A/G]GTATGTGGGAAGGGA | 108660 |
| rs49485933 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934572 | TGGATGTTGGTCTCA[C/T]GGGCCACCAGCTGGC | 108660 |
| rs49740425 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934837 | CTTCCCAAATGAATC[C/T]TTTTTTTTTTTTTTT | 108660 |
| rs49778455 | snp | C/G | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940537 | TACTGAGGTCTGGCG[C/G]TCAAACCCAGGGCAT | 108660 |
| rs50012016 | snp | A/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58933725 | GATGAGGATGAGGGA[A/T]GACAGGGGGGATACC | 108660 |
| rs50034408 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934352 | TCAAAATAAGCTGGG[A/T]CTTTTGAATTAAATC | 108660 |
| rs50123141 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58933705 | GTCCAAGACTCGGGG[A/C]ATGAGATGAGGATGA | 108660 |
| rs50194099 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934466 | TCTGACATCCCTTAT[A/G]GTGGTATTAGCTTGG | 108660 |
| rs50723312 | snp | A/G | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933023 | ATGCCACACTAAGCT[A/G]AGCCATGGCAAAACA | 108660 |
| rs51022380 | snp | A/G | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940732 | AAGGATGAAGGACAC[A/G]TGGGAAGATACGATG | 108660 |
| rs51101069 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933579 | CTCTGAGGTTGTATA[A/G]GCCCCAAACAGCTGA | 108660 |
| rs51144340 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58935289 | CCTGTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs51244561 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934366 | GACTTTTGAATTAAA[C/T]CTACTTTAAAAACTA | 108660 |
| rs51276665 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933476 | ACACAGGTATAGACA[A/G]TAAGACAGAGTGCTG | 108660 |
| rs51542884 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934521 | GCAGGGCCTTGCAGC[G/T]CTCCATCACTCATGT | 108660 |
| rs51583444 | snp | C/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934935 | AGACCAGGCTGGCTT[C/G]GAACTCAGAAATCCT | 108660 |
| rs51724166 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934476 | CTTATGGTGGTATTA[A/G]CTTGGTCCCACTGTC | 108660 |
| rs51766213 | snp | A/G | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940719 | ATGGATGGGAAGCAA[A/G]GATGAAGGACACGTG | 108660 |
| rs52027959 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934451 | ACATGAAAGGATGCC[C/T]CTGACATCCCTTATG | 108660 |
| rs52629277 | snp | C/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934878 | GTTTTTTTGAGACAG[C/G]GTTTCTCTGTGTAGC | 108660 |
| rs52644463 | snp | A/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940189 | CTGTCTCAAAAATAA[A/T]TAAATAAATAAATAA | 108660 |
| rs211908727 | in-del | -/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934308 | TTAAAGAAAGAGAAG[-/C]GCCCTCTACTCTGAA | 108660 |
| rs211946459 | in-del | -/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58935314 | GAGCCATCTGCATCC[-/T]CTCCTTCCCTGTGTT | 108660 |
| rs212309403 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936238 | CAGCCAGATAACAGC[C/T]GTCTGGCCAAGCTCC | 108660 |
| rs212690664 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937128 | TCCCCATATCCAGGA[G/T]AGCCCACTTACCTTC | 108660 |
| rs213043928 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934950 | CGAACTCAGAAATCC[G/T]CCTGCCTCTGCCTCC | 108660 |
| rs214047589 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58936205 | GGAAGAATGTTTTTG[A/C]TGAAAGGACATAAAT | 108660 |
| rs214088811 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940148 | CACAGTGAGTTTCAG[G/T]CCAATCAAAGCTATA | 108660 |
| rs214092284 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939084 | CTTCCACACTGGTTC[C/T]CGTAGCAGCTCACGA | 108660 |
| rs214404009 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58938009 | GCTTGCACCGATGAA[A/G]TCACACCGGGATAGG | 108660 |
| rs214430100 | in-del | -/AAATAAATAAATAAATAAAT | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940183 | AAGACCCTGTCTCAA[-/AAATAAATAAATAAATAAAT]AAATAAATAAATAAA | 108660 |
| rs214478796 | in-del | -/CT | | | intron-variant | Rnf187 | Mm_Celera | 11:58933948 | TCTCTTCCACCGTGG[-/CT]CTGAGTTGACTAGAG | 108660 |
| rs214756284 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58935228 | TCAAGATCCTTCTAT[A/G]AAACGGCACAACATT | 108660 |
| rs215088615 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934346 | ATGCTCTCAAAATAA[G/T]CTGGGACTTTTGAAT | 108660 |
| rs215740619 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934317 | AGAGAAGGCCCTCTA[C/T]TCTGAAAGAAATTAT | 108660 |
| rs215878405 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939289 | ACTTATCGCTATACC[G/T]TCAGCCCTGAAGCAG | 108660 |
| rs216198947 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937860 | CGGTGGCAGGTGCTA[C/T]GTGCAATGACCAAGA | 108660 |
| rs216400241 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935003 | GTGCCACCACCGCCT[A/G]GCCCAAATGAATCAC | 108660 |
| rs216882980 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58937566 | AGCAGTATGTTCTGA[A/C]AGAGTGTATCTACCT | 108660 |
| rs217010604 | in-del | -/CACACC | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58932143 | GGGTTTGGGATGACA[-/CACACC]CACACCCACACCCAC | 108660 |
| rs217335444 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939746 | CCTGCCTTGATAATG[A/G]ACTGAACCTCTAAAC | 108660 |
| rs217485034 | in-del | -/A | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939635 | TGAGACCTCACTCTT[-/A]AGCTGCGGGAAACAG | 108660 |
| rs217506487 | in-del | -/CTC | | | intron-variant | Rnf187 | Mm_Celera | 11:58934759 | ACAAAGGCTACCTCT[-/CTC]CTCCTACACAGCGAT | 108660 |
| rs218239915 | in-del | -/G | | | utr-variant-5-prime | Rnf187 | Mm_Celera | 11:58938791 | GAGCGCCAGGGCTGC[-/G]GGCGGCGGCGCCGAC | 108660 |
| rs218951326 | in-del | -/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58935252 | CAACATTAACACAGA[-/T]GCCATCTGCATCCTC | 108660 |
| rs218960248 | snp | A/G | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933002 | GGTTCCTGGATACTA[A/G]AACGAATGCCACACT | 108660 |
| rs219127256 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58933600 | AAACAGCTGATGGGT[A/C]TGTGGGAAGGGAATA | 108660 |
| rs219748183 | in-del | -/A | | | intron-variant | Rnf187 | Mm_Celera | 11:58933441 | GAAAGACAGGGAGAC[-/A]AGAGAAAATGAAGGG | 108660 |
| rs220186581 | in-del | -/AAC | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940686 | AAACCAAACAAAGAT[-/AAC]AACAAAAACCATAGC | 108660 |
| rs220262860 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58936697 | CCAGGCAATGGTGTT[A/G]AGTGGTGGGCCTTTG | 108660 |
| rs220488812 | snp | C/T | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58931959 | CACCCTGGGTATGAA[C/T]GTGACCAGTCTGTTA | 108660 |
| rs220625475 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934633 | CCACCTTGGGTGCAT[G/T]CACTAGACACAGTAG | 108660 |
| rs221099613 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939687 | GGATGTAGAACTCTC[A/G]GTTCCTTCTCCAGAG | 108660 |
| rs221454719 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940700 | TAACAACAAAAACCA[G/T]AGCATGGATGGGAAG | 108660 |
| rs221548563 | snp | A/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936345 | AACTAGGTGTCCTCA[A/T]TGTCTTCCAATTTTT | 108660 |
| rs221695764 | snp | A/G | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58932030 | tgcagaccctgtctg[A/G]tgggctaagccagag | 108660 |
| rs221729693 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58938314 | GATGCGGGAGAGGGA[A/C]GAGGAGGTCAGCACA | 108660 |
| rs222173486 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936392 | GTGCCTTCAGCCTTA[C/T]GGCGCAGACCATCTG | 108660 |
| rs222416940 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939371 | CCAAATTAAGATAGC[A/G]ACATAAAATGAAGTC | 108660 |
| rs224203135 | in-del | -/A | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940444 | TAAAATTAATTAAAT[-/A]AAAAAATCAGTTGTA | 108660 |
| rs224314738 | in-del | -/AAAA | | | intron-variant | Rnf187 | Mm_Celera | 11:58936456 | TTTGGTTTTATGTTT[-/AAAA]TAAAAAAAATGGGCA | 108660 |
| rs224341954 | in-del | -/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934862 | TTTTTTTTTTTTTTT[-/G]GTTTTTTTGAGACAG | 108660 |
| rs224428218 | in-del | -/AAACAAAC | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58936561 | AGTAACCTAAAAACA[-/AAACAAAC]AAACAAACAAACTGT | 108660 |
| rs225735287 | in-del | -/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935749 | CGTACACTAAGTGCA[-/C]CGTGTAAGCACCAGG | 108660 |
| rs225944463 | in-del | -/AG | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940294 | GTGTGTGTGTGTGTA[-/AG]AGAGAGAGAGAGAGA | 108660 |
| rs226007441 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934943 | CTGGCTTCGAACTCA[A/G]AAATCCTCCTGCCTC | 108660 |
| rs226022682 | in-del | -/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940377 | AATTGTGGTATCCTT[-/G]GGGGTTTAGAGCCAA | 108660 |
| rs226179857 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58933814 | GCATCTCCTAGCTTC[A/G]TCAGCTCTAAGTTCC | 108660 |
| rs226506658 | snp | A/G | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58931848 | CCCAACAGAGACCAC[A/G]TTCTGTCACTGAGGA | 108660 |
| rs226555545 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58933489 | CAGTAAGACAGAGTG[C/T]TGCTATCCTGCGTAC | 108660 |
| rs226678643 | snp | C/G | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58932830 | GGAATACTGCATTAA[C/G]ACTCAGGTCCCAGCC | 108660 |
| rs227074810 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58937942 | GGCTGCAAATGGTAA[A/C]TGGTAGACCAAAGAC | 108660 |
| rs227130249 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58938996 | CTCCATCCAGGTCCT[G/T]GCAGCTGTGCGCTCT | 108660 |
| rs227416910 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934984 | GTGCTGGGATTAAAG[A/G]CGTGTGCCACCACCG | 108660 |
| rs227690360 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58933592 | TAGGCCCCAAACAGC[C/T]GATGGGTATGTGGGA | 108660 |
| rs228331483 | snp | A/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934258 | GAGGGGGAAGGGACA[A/T]CGGTCCACACTGGAC | 108660 |
| rs228611807 | snp | A/C | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939973 | GCACAGTATTCACAT[A/C]CTGTTAAGTATCATA | 108660 |
| rs228705484 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58936641 | GGTGAAGGCTAGCTA[A/C]GTACCAAATCttgtg | 108660 |
| rs228905694 | snp | G/T | | | synonymous-codon | Rnf187 | Mm_Celera | 11:58938764 | GCAGATGGCATCAGC[G/T]GGGCCCGCGGGGAGC | 108660 |
| rs228985363 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934294 | CTGCTGCCAATGTGT[C/T]TAAAGAAAGAGAAGG | 108660 |
| rs229451855 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939091 | ACTGGTTCCCGTAGC[A/G]GCTCACGACCTTTGT | 108660 |
| rs229483924 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937734 | CCTGTCGGGCGGAGA[C/T]CACGGCTTTCCTACC | 108660 |
| rs229662170 | snp | A/G | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58932242 | CCTGGTCAGGGAAGG[A/G]GGAAGCAGCTGTGTA | 108660 |
| rs229758831 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936929 | GAAAACAGAATGTTC[C/T]ACTGGTAACAGCTGG | 108660 |
| rs231521790 | in-del | -/A | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940227 | AATAAATAAATAAAT[-/A]AAAGTGTGTGTCTGT | 108660 |
| rs231877555 | snp | A/G | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933128 | GGTAGGTCTCTATTT[A/G]GAACAGGTACAAGCC | 108660 |
| rs231933224 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58933699 | GTGTTGGTCCAAGAC[G/T]CGGGGAATGAGATGA | 108660 |
| rs232977595 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58936368 | CAATTTTTGTGAAAG[A/G]TAGAGCAGGTGCCTT | 108660 |
| rs233031934 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937462 | CAGCTTGATTTAAGA[C/T]AGTGACTTTCCTGAC | 108660 |
| rs233361968 | in-del | -/TA | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939609 | AAGTGTGTCACTGTG[-/TA]GCCGTGGGCTTTGAG | 108660 |
| rs233811861 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939295 | CGCTATACCTTCAGC[C/T]CTGAAGCAGGATAAA | 108660 |
| rs234049694 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940340 | AGAGAAACATTTTAT[C/T]TGAGGGATTGGAGTG | 108660 |
| rs234435958 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58935071 | GTGTATTGTAAGATG[C/T]GACAGCTTCTTTGGG | 108660 |
| rs235167223 | in-del | -/AAATAAATAAATAAATAAATAAAT | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940182 | AAGACCCTGTCTCAA[-/AAATAAATAAATAAATAAATAAAT]AAATAAATAAATAAA | 108660 |
| rs235197767 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934480 | TGGTGGTATTAGCTT[A/G]GTCCCACTGTCGTGA | 108660 |
| rs235336598 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940156 | GTTTCAGGCCAATCA[A/G]AGCTATATAGTAAGA | 108660 |
| rs235544250 | snp | C/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58938017 | CGATGAAATCACACC[C/G]GGATAGGAGCAAGAG | 108660 |
| rs235585853 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939233 | CCATCTCCCACAGAT[A/G]ATTTGGGAGGTGGTC | 108660 |
| rs235739515 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58937831 | CACACAGAGTCTAAT[A/G]GTCGGTTTCTGCCCG | 108660 |
| rs235918314 | snp | C/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934461 | ATGCCTCTGACATCC[C/G]TTATGGTGGTATTAG | 108660 |
| rs236391994 | snp | A/C | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939974 | CACAGTATTCACATC[A/C]TGTTAAGTATCATAA | 108660 |
| rs236541479 | in-del | -/ACA | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58936264 | CTCCTCCCTCTGACC[-/ACA]GGACCCCCATCTTCG | 108660 |
| rs236561015 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936234 | ATGCCAGCCAGATAA[C/T]AGCTGTCTGGCCAAG | 108660 |
| rs236998218 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939386 | GACATAAAATGAAGT[C/T]AGGGAGTCTCACTGT | 108660 |
| rs237253934 | snp | A/G | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58932921 | CTGGTGCGCCTCAGA[A/G]CCTTGCTGAGGGATG | 108660 |
| rs237328477 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937549 | AACCATAGGACAACC[C/T]CAGCAGTATGTTCTG | 108660 |
| rs237506272 | in-del | -/A | | | intron-variant | Rnf187 | Mm_Celera | 11:58937266 | TTAGAGCCTGGGAAG[-/A]AGGATTTGAACACCC | 108660 |
| rs237693605 | in-del | -/TGTGTGTGTGTGTGTG | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940270 | TGAGTGAAAGAGAAT[-/TGTGTGTGTGTGTGTG]TGTGTATGTGTGTGT | 108660 |
| rs238036155 | snp | C/T | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58932010 | TGCGCAGCTGGCCAG[C/T]CCTCTGCAGACCCTG | 108660 |
| rs239157331 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934621 | TTACAGAGGGAACCA[C/T]CTTGGGTGCATTCAC | 108660 |
| rs239304198 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935686 | CACTGGATACAATTT[A/C]CCTAACACAACATAA | 108660 |
| rs239820459 | in-del | -/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58936652 | CTAAGTACCAAATCT[-/G]TGTGTCCCCAAATCT | 108660 |
| rs240016299 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934906 | AGCCCTGGCTGTCCT[A/G]GAACTCACTCTGTAG | 108660 |
| rs240315315 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58937607 | CCTGGATGTAACCAC[A/C]GGCCTCCACCTCAAA | 108660 |
| rs240512954 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939478 | CTGTAGTCAGCTATC[C/T]GCAATGTGTGACTCT | 108660 |
| rs240543423 | in-del | -/ACT | | | intron-variant | Rnf187 | Mm_Celera | 11:58936261 | AAGCTCCTCCCTCTG[-/ACT]ACCGGACCCCCATCT | 108660 |
| rs240644957 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937309 | TGGCGACTGGAACTA[C/T]TCGTCCGGTCTCTGC | 108660 |
| rs241200766 | snp | A/G | | | utr-variant-5-prime | Rnf187 | Mm_Celera | 11:58938852 | CCGAGGACCGGCCGG[A/G]GATCAAGGCCGACGA | 108660 |
| rs241539675 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940705 | ACAAAAACCATAGCA[C/T]GGATGGGAAGCAAGG | 108660 |
| rs241566919 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58933959 | CGTGGCTGAGTTGAC[C/T]AGAGATGTGCTGTGG | 108660 |
| rs241612121 | snp | A/G | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58932280 | ACTAGGAGGTATGGA[A/G]ACAGAGAGGCTGGAG | 108660 |
| rs241668076 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935720 | CCTTTGTAAAGAGCT[A/G]ACTAGAAAGAAGTCC | 108660 |
| rs241873431 | snp | A/G | | | synonymous-codon | Rnf187 | Mm_Celera | 11:58938502 | CGGCGCGACAGAGCA[A/G]CTGCAGCGCGGCCTC | 108660 |
| rs242695335 | snp | A/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937558 | ACAACCCCAGCAGTA[A/T]GTTCTGACAGAGTGT | 108660 |
| rs243130812 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58936396 | CTTCAGCCTTACGGC[A/G]CAGACCATCTGAGGG | 108660 |
| rs243236671 | in-del | -/GGG | | | intron-variant | Rnf187 | Mm_Celera | 11:58937524 | TTGCTGTCTTAGTAA[-/GGG]GACGACAAACCATAG | 108660 |
| rs244516289 | snp | C/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933360 | GTTCCTTCTGCCTCG[C/T]GCTCCAGGGGGCCAG | 108660 |
| rs244527065 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939734 | GCTGTCATGCTTCCT[A/G]CCTTGATAATGGACT | 108660 |
| rs244625057 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937737 | GTCGGGCGGAGACCA[C/T]GGCTTTCCTACCTGG | 108660 |
| rs244740613 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937968 | AAGACCACTCTCAGG[G/T]CTCCATAAGCAAGTG | 108660 |
| rs244796225 | snp | A/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939076 | TGAGCTCTCTTCCAC[A/T]CTGGTTCCCGTAGCA | 108660 |
| rs245114687 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58933560 | AGGGGTCCAAAGCCT[A/G]TGTCTCTGAGGTTGT | 108660 |
| rs245857766 | snp | C/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58933616 | TGTGGGAAGGGAATA[C/G]CTCAGTTACAGGTGG | 108660 |
| rs246151530 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58936181 | ACAGGGGACACCCAT[A/G]TTCCTGAAGGAAGAA | 108660 |
| rs246202612 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58936922 | GCAGCCAGAAAACAG[A/G]ATGTTCTACTGGTAA | 108660 |
| rs246255803 | snp | C/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934309 | TTAAAGAAAGAGAAG[C/G]CCCTCTACTCTGAAA | 108660 |
| rs246630325 | in-del | -/GCT | | | intron-variant | Rnf187 | Mm_Celera | 11:58936636 | ATCAGGTGAAGGCTA[-/GCT]GCTAAGTACCAAATC | 108660 |
| rs246913899 | in-del | -/CA | | | intron-variant | Rnf187 | Mm_Celera | 11:58933958 | CGTGGCTGAGTTGAC[-/CA]TAGAGATGTGCTGTG | 108660 |
| rs247024165 | snp | C/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58937835 | CAGAGTCTAATAGTC[C/G]GTTTCTGCCCGGTGG | 108660 |
| rs247319914 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940580 | GCAATGACTGTACTT[G/T]TAATCCCAGCAATTG | 108660 |
| rs247448406 | snp | A/G | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58932473 | GGTTTTGTTTCTTGG[A/G]CTAGTTATCTACACA | 108660 |
| rs248407352 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934272 | AACGGTCCACACTGG[A/C]CCATACCTGCTGCCA | 108660 |
| rs248546896 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935649 | AGCCACCTGCATCCC[C/T]CCCTGTGCTGCAGGT | 108660 |
| rs249233113 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939093 | TGGTTCCCGTAGCAG[C/T]TCACGACCTTTGTCC | 108660 |
| rs249381699 | snp | G/T | | | utr-variant-3-prime | Rnf187 | Mm_Celera | 11:58933210 | CTATGTGCATGGCCA[G/T]CGGGGCACCTCTGAT | 108660 |
| rs249890877 | snp | A/G | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58931952 | ACCCAGTCACCCTGG[A/G]TATGAATGTGACCAG | 108660 |
| rs250559349 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936378 | GAAAGGTAGAGCAGG[C/T]GCCTTCAGCCTTACG | 108660 |
| rs250617935 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937503 | CCTGCTTGGTCTTTG[G/T]GGAGATTGCTGTCTT | 108660 |
| rs251653550 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940535 | GTTACTGAGGTCTGG[C/T]GCTCAAACCCAGGGC | 108660 |
| rs251722083 | snp | A/T | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58931953 | CCCAGTCACCCTGGG[A/T]ATGAATGTGACCAGT | 108660 |
| rs252768270 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58936311 | AACCTATCCTTGGAA[C/T]TGCTGTGGGCTTGTA | 108660 |
| rs253248072 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58935173 | CCTTCATGACTGATT[C/T]CAGGAACTGCATCCC | 108660 |
| rs254243133 | in-del | -/CT | | | intron-variant | Rnf187 | Mm_Celera | 11:58934755 | CAGAACAAAGGCTAC[-/CT]CTCTCTCCTACACAG | 108660 |
| rs254337451 | snp | G/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58938310 | ATGGGATGCGGGAGA[G/T]GGAAGAGGAGGTCAG | 108660 |
| rs254341134 | in-del | -/A | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940000 | CATAAGTCATCTAGG[-/A]AAAAAATATTACATA | 108660 |
| rs254412434 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939281 | CCAGGGTGACTTATC[G/T]CTATACCTTCAGCCC | 108660 |
| rs254528437 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58936042 | GACTTCTGATAAACC[C/T]GAGAGCAAAACTCGG | 108660 |
| rs255268096 | snp | G/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939393 | AATGAAGTCAGGGAG[G/T]CTCACTGTGCACACA | 108660 |
| rs255867492 | snp | A/G | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58932224 | GTATCAAAGTCCTTG[A/G]AACCTGGTCAGGGAA | 108660 |
| rs255915642 | in-del | -/AC | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940739 | AGGACACGTGGGAAG[-/AC]ATACGATGTAACCTG | 108660 |
| rs256095420 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58938234 | GCAGAATCACGGACT[C/T]CAGGATCCAAGAGCC | 108660 |
| rs256297433 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937550 | ACCATAGGACAACCC[C/T]AGCAGTATGTTCTGA | 108660 |
| rs256471161 | in-del | -/GCCCT | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939038 | TGGTATTCGCTCATC[-/GCCCT]GCCCTGCCCATGATT | 108660 |
| rs257689922 | snp | C/G | | | synonymous-codon | Rnf187 | Mm_Celera | 11:58938407 | CACCTTGCCGCGCAG[C/G]GCCTTCCTCCAGCGC | 108660 |
| rs258003135 | in-del | -/CTC | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58931791 | GGTGGCCTAGACCTT[-/CTC]CACACCTGCTAGTCT | 108660 |
| rs258345239 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58938367 | GTAAGCCACAAAGGT[A/G]GACAGTGTGCAGGGG | 108660 |
| rs258478913 | snp | G/T | | | utr-variant-5-prime | Rnf187 | Mm_Celera | 11:58938855 | AGGACCGGCCGGAGA[G/T]CAAGGCCGACGAGCC | 108660 |
| rs258545263 | in-del | -/CCC | | | intron-variant | Rnf187 | Mm_Celera | 11:58934764 | GGCTACCTCTCTCCT[-/CCC]ACACAGCGATTTCAT | 108660 |
| rs258546630 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58939479 | TGTAGTCAGCTATCT[A/G]CAATGTGTGACTCTT | 108660 |
| rs259101376 | in-del | -/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934444 | AATCTCCACATGAAA[-/G]GATGCCTCTGACATC | 108660 |
| rs259181683 | snp | A/C | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940768 | TGGAAGGTGGCCCAG[A/C]GCATGGGCATCCCTG | 108660 |
| rs259337774 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58933501 | GTGCTGCTATCCTGC[A/G]TACAATGCACACAGA | 108660 |
| rs259399027 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58933987 | TGGAAAGAGGTGCTC[A/C]CCCCCTGCCCAGGTG | 108660 |
| rs259868632 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935002 | TGTGCCACCACCGCC[C/T]AGCCCAAATGAATCA | 108660 |
| rs260471992 | in-del | -/TC | | | intron-variant | Rnf187 | Mm_Celera | 11:58937714 | GCTAAGCTACGATTT[-/TC]TCTCCTGTCGGGCGG | 108660 |
| rs260745767 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940235 | AATAAATAAAAGTGT[A/G]TGTCTGTGTGTCTGT | 108660 |
| rs260959195 | snp | A/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58938146 | TGAAAGGGGGACGGA[A/G]GAGCATGCGCTAGAG | 108660 |
| rs261221563 | snp | A/C | | | intron-variant | Rnf187 | Mm_Celera | 11:58937802 | ACTCTATCTAGATCC[A/C]TGCAACCCATCTTCA | 108660 |
| rs261302922 | in-del | -/TTTTTG | | | intron-variant | Rnf187 | Mm_Celera | 11:58934857 | TTTTTTTTTTTTTTT[-/TTTTTG]GTTTTTTTGAGACAG | 108660 |
| rs261436510 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940706 | CAAAAACCATAGCAT[A/G]GATGGGAAGCAAGGA | 108660 |
| rs261893355 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935851 | CACCAACCAGACACA[C/T]TCTCATTTCTGAGTA | 108660 |
| rs262024023 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934234 | CCATAACATGCCCCT[A/G]CAGGGTGAGAGGGGG | 108660 |
| rs262554890 | snp | A/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940668 | TGGCTTAAAAGAAAA[A/G]CCAAACCAAACAAAG | 108660 |
| rs262578845 | snp | C/T | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940524 | GTTCTCAAATTGTTA[C/T]tgaggtctggcgctc | 108660 |
| rs262779344 | in-del | -/TGTGTGTGTGTGTGTG | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940276 | AAAGAGAATTGTGTA[-/TGTGTGTGTGTGTGTG]TGTGTGTGTGTGTGT | 108660 |
| rs264060504 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58934677 | ATCTTTGACCTTCAG[C/T]CACTAGAACTCATAA | 108660 |
| rs265220568 | snp | C/T | | | intron-variant | Rnf187 | Mm_Celera | 11:58937638 | AGTGTTCTTCACAAC[C/T]TATTCCAGAGGCTCA | 108660 |
| rs265292122 | in-del | -/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58938253 | ATCCAAGAGCCCCTA[-/G]GCATGGCAGGGTCCC | 108660 |
| rs266215563 | snp | C/G | | | downstream-variant-500B | Rnf187 | Mm_Celera | 11:58932286 | AGGTATGGAAACAGA[C/G]AGGCTGGAGCAAACC | 108660 |
| rs387035093 | in-del | -/CAA | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940691 | AAACAAAGATAACAA[-/CAA]AAACCATAGCATGGA | 108660 |
| rs387113969 | in-del | -/AAAC | | | intron-variant | Rnf187 | Mm_Celera | 11:58936577 | AACAAACAAACAAAC[-/AAAC]TGTAACATAATGTCA | 108660 |
| rs387174141 | in-del | -/G | | | intron-variant | Rnf187 | Mm_Celera | 11:58934445 | ATCTCCACATGAAAG[-/G]ATGCCTCTGACATCC | 108660 |
| rs387367459 | in-del | -/TAAA | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940226 | AAATAAATAAATAAA[-/TAAA]AGTGTGTGTCTGTGT | 108660 |
| rs387589936 | in-del | -/AAAC | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58936561 | AGTAACCTAAAAACA[-/AAAC]AAACAAACAAACAAA | 108660 |
| rs387757331 | in-del | -/G | | | upstream-variant-2KB | Rnf187 | Mm_Celera | 11:58940381 | GTGGTATCCTTGGGG[-/G]TTTAGAGCCAACCTC | 108660 |
| rs578270066 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935736 | ACTAGAAAGAAGTCC[A/G]TACACTAAGTGCACG | 108660 |
| rs579070404 | snp | C/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58937274 | TGGGAAGAAGGATTT[C/G]AACACCCCGATCAGC | 108660 |
| rs579483891 | snp | A/T | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940193 | CTCAAAAATAAATAA[A/T]TAAATAAATAAATAA | 108660 |
| rs579946315 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935299 | AGGTCCTCTAACACA[A/G]AGCCATCTGCATCCT | 108660 |
| rs580970928 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58936469 | TTTTAAAAAAAATGG[A/G]CAGGGAACTATAATG | 108660 |
| rs581317284 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935337 | CCTGTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs581565914 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935633 | AGGTCATCTAACACA[A/G]AGCCACCTGCATCCC | 108660 |
| rs582645305 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58937709 | AACACGCTAAGCTAC[A/G]ATTTTCTCTCCTGTC | 108660 |
| rs582777084 | snp | G/T | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939029 | TTTCAGGTTCTGGTA[G/T]TCGCTCATCGCCCTG | 108660 |
| rs582899457 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933425 | ACAAACAGACAAAGG[A/G]GAAAGACAGGGAGAC | 108660 |
| rs583013758 | snp | C/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934832 | TTATGCTTCCCAAAT[C/G]AATCTTTTTTTTTTT | 108660 |
| rs583243527 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935328 | CTCTCCTTCCCTGTG[C/T]TTCAGGTCCTCTAAC | 108660 |
| rs583491959 | snp | A/T | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940201 | TAAATAAATAAATAA[A/T]TAAATAAATAAATAA | 108660 |
| rs583663021 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935470 | CTCTCCTTCCCTGTG[C/T]TTCAGGTCCTCTAAC | 108660 |
| rs584161662 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935639 | TCTAACACAGAGCCA[C/T]CTGCATCCCCCCCTG | 108660 |
| rs584543604 | snp | A/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58936627 | CATGGGTGGTATCAG[A/G]TGAAGGCTAGCTAAG | 108660 |
| rs585163870 | snp | C/T | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58939629 | TGGGCTTTGAGACCT[C/T]ACTCTTAGCTGCGGG | 108660 |
| rs585416121 | snp | C/G | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58934936 | GACCAGGCTGGCTTC[C/G]AACTCAGAAATCCTC | 108660 |
| rs585716602 | snp | A/G | | | upstream-variant-2KB | Rnf187 | GRCm38.p3 | 11:58940385 | TATCCTTGGGGGTTT[A/G]GAGCCAACCTCTTCA | 108660 |
| rs587251939 | snp | G/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935330 | CTCCTTCCCTGTGTT[G/T]CAGGTCCTCTAACAC | 108660 |
| rs587496488 | snp | A/C | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935575 | CCTGTGTTTCAGGTC[A/C]TCTAACACAGAGCCA | 108660 |
| rs864260067 | in-del | -/A | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58933774 | GAGCCTAAGGTGGGG[-/A]AAAACCCTCCCAGTG | 108660 |
| rs864315535 | snp | C/T | | | intron-variant | Rnf187 | GRCm38.p3 | 11:58935591 | TCTAACACAGAGCCA[C/T]CTGCATCCTCTCCTT | 108660 |