SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6351678 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Ercc8 | Mm_Celera | 13:108183678 | GTCTTTGTTGCCGTT[A/T]TAGCTCAGGCTTTAG | 71991 |
rs13459870 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108174023 | CAAGGTACAACTTTG[C/T]GACTTAAAGTCTGGA | 71991 |
rs13459871 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108194472 | TAAAATGAGATCGAT[A/G]TGTATGATACCCTGA | 71991 |
rs13459872 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108194677 | ACTCCTGACTGTGCT[G/T]CCAGCCTGCCCTTCC | 71991 |
rs29225283 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Ercc8 | Mm_Celera | 13:108172259 | AACAGAGAGAGTGGT[A/G]TTGGATGTGTTGGAC | 71991 |
rs29226951 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108187012 | AAGTTATGCCAACAT[A/C]ATGCACAAAATTTAA | 71991 |
rs29227339 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Ercc8 | Mm_Celera | 13:108169265 | TGTGATCCTACTGTA[A/G]AAATCCATATCTTCT | 71991 |
rs29231754 | snp | G/T | 0.5 | 0 | downstream-variant-500B | Ercc8 | Mm_Celera | 13:108199371 | ATCCCATTACAAATG[G/T]TTGTGAGTCACCATG | 71991 |
rs29232857 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108194517 | TCGGTTAATTAATCA[A/G]AACTTGTCTCCTTGA | 71991 |
rs29236744 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ercc8 | Mm_Celera | 13:108193477 | GAACTATAGTGAGCG[G/T]GGCTGAGAGGGTGGC | 71991 |
rs29238396 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108163922 | GAAATATTTCCAAAA[C/T]GAACCAAAGCCTAAG | 71991 |
rs29239490 | snp | C/T | 0.5 | 0 | intron-variant | Ercc8 | Mm_Celera | 13:108185028 | TGAAGCTGGGCTGGC[C/T]ATCAACTGTCCCTAG | 71991 |
rs29239499 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108187156 | CTTGATAGAGCTCAT[C/T]TCAGCTTTCGATTGA | 71991 |
rs29249882 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Ercc8 | Mm_Celera | 13:108168993 | GTGTGGAACAGTCCA[C/T]AGTTCTAATAATGAT | 71991 |
rs29251300 | snp | A/G/T | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | GRCm38.p3 | 13:108194424 | AGTTTTTAACCTGTT[A/G/T]ATCCTGAGTTTGGGA | 71991 |
rs29251317 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108197852 | GCAGGGAGACATGGC[A/G]CTGGAGAGGTAGCTA | 71991 |
rs29252235 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108197877 | TAGCTAAGAGTTGTA[C/T]GTCTGAGTCTGCAGA | 71991 |
rs29492927 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108192548 | AAGACAATTTAACAC[C/T]AGGCTTACAATTTGT | 71991 |
rs29496156 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Ercc8 | Mm_Celera | 13:108178568 | AAATGTGTTTTCATT[A/G]CAGCAAACACTGCTC | 71991 |
rs29508287 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Ercc8 | Mm_Celera | 13:108170732 | TACGCTGACAGTGCC[A/G]GTTTGTGAGTCAGGA | 71991 |
rs29510361 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108191545 | GTTGTAGAGCAAACC[C/G]AAGCCGGGGACTCTC | 71991 |
rs29514518 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Ercc8 | Mm_Celera | 13:108192603 | GGCAGATGCAGAGCT[A/G]CAGAATGACAAACAG | 71991 |
rs29516437 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Ercc8 | Mm_Celera | 13:108168624 | GGCTCGAACAGGGAA[C/T]GTGACAGAAATGATG | 71991 |
rs29527527 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108160512 | TAATAAATCTGAATA[C/T]CTTTAAATGTAGTAA | 71991 |
rs29532072 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108160069 | CCTCCGCTTCACTTC[A/G]TTTTAACTGTGGCAT | 71991 |
rs29547155 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ercc8 | Mm_Celera | 13:108193644 | CTCCAAAGGGGGCTG[A/G]GGTTATTAAATTATC | 71991 |
rs29549193 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Ercc8 | Mm_Celera | 13:108180386 | AATACTGAGATACCA[A/G]ATAGAGGGCAGAGTT | 71991 |
rs29551869 | snp | A/C | 0.459184 | 0.136902 | intron-variant | Ercc8 | Mm_Celera | 13:108192049 | GGCTCCAGAGTGGGA[A/C]GTTTACAGACATGTC | 71991 |
rs29552457 | snp | G/T | 0.375 | 0.216506 | downstream-variant-500B | Ercc8 | Mm_Celera | 13:108199490 | AGTGAGGGGACTGGA[G/T]AGAGTGGTCAGCAGT | 71991 |
rs29566957 | snp | A/C | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108186419 | GGGTGTAGTCCTATG[A/C]CACCACTCCCAACCA | 71991 |
rs29571993 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Ercc8 | Mm_Celera | 13:108187728 | GCACCACCATGCCCA[C/T]CTACTATTTGGAAAC | 71991 |
rs29573643 | snp | C/T | 0.5 | 0 | intron-variant | Ercc8 | Mm_Celera | 13:108192372 | TATCACTGTGTGTTT[C/T]CTAGCTGGCCTATCT | 71991 |
rs29576441 | snp | C/G | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108181324 | AAAGTTCCTTAATCT[C/G]TTATCTCCTAGAACA | 71991 |
rs29582916 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ercc8 | Mm_Celera | 13:108185756 | TGTCAGTTCCTAAGC[A/G]TCCCTAACTCTGGTT | 71991 |
rs29587350 | snp | C/T | 0.48 | 0.0979796 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108194758 | AGTGGCATCATAATG[C/T]TAGATTTTTTACTCA | 71991 |
rs29672502 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Ercc8 | Mm_Celera | 13:108177502 | TAATCCAGTACAACT[G/T]TAGGAATATATTTGT | 71991 |
rs29678805 | snp | A/G | 0.444444 | 0.157135 | missense, intron-variant, nc-transcript-variant, upstream-variant-2KB | Ercc8, Gm32268 | Mm_Celera | 13:108166484 | AAAGCAGTGTGTTCC[A/G]TTGGCAGGTGTGTAT | 71991 |
rs29685616 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108160104 | AATAGTTTGTATTTC[C/T]ACAGTCTTAGACATC | 71991 |
rs29735274 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Ercc8 | GRCm38.p3 | 13:108173551 | AGTTGCTAGGATGCT[G/T]TTTCTACCAATTGGA | 71991 |
rs29766537 | snp | G/T | 0.401235 | 0.199068 | intron-variant | Ercc8 | Mm_Celera | 13:108170632 | GTGGGAGTTAGGGAG[G/T]TTATTACGACCTAAG | 71991 |
rs29772238 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Ercc8 | Mm_Celera | 13:108192610 | GCAGAGCTGCAGAAT[A/G]ACAAACAGACCTGAT | 71991 |
rs29775120 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Ercc8 | Mm_Celera | 13:108186946 | TCTATAGAAGGCACA[A/G]ATTGGTATGAAATCT | 71991 |
rs29784601 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Ercc8 | Mm_Celera | 13:108172523 | ATAGAGAGGAATGGT[A/G]AGCCAGAGGCTTGCT | 71991 |
rs29827919 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Ercc8, Gm32268 | Mm_Celera | 13:108166906 | TCACCACACACACAC[A/G]TGCCCCCTCTCTTGT | 71991 |
rs29867381 | snp | C/T | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108186560 | AACTGCATCAGCCCA[C/T]GGGTCCTTCCTGTCA | 71991 |
rs29870220 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ercc8 | Mm_Celera | 13:108186918 | GATTCCAGTAGGGCA[A/G]TTGATACTCATCTAT | 71991 |
rs29875277 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108160503 | GGCCTACATTAATAA[A/G]TCTGAATACCTTTAA | 71991 |
rs29878922 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108160531 | TAAATGTAGTAAGAA[A/G]CTAAAGCCTTGCAGA | 71991 |
rs29920231 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Ercc8, Gm32268 | GRCm38.p3 | 13:108162262 | AGTATATTAGTAGCC[C/G/T]GGCGTGCTGGCACAC | 71991 |
rs29950343 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108160345 | TGAATCATAACAGAA[A/G]CACAGTTTCAGTTAT | 71991 |
rs29964257 | snp | A/C/T | 0.265928 | 0.249492 | intron-variant | Ercc8 | GRCm38.p3 | 13:108175536 | TTTGTAAAATACTTC[A/C/T]TTCACTCGTGCTTGC | 71991 |
rs30004840 | snp | A/G | 0.5 | 0 | intron-variant | Ercc8 | Mm_Celera | 13:108193776 | CTGTCTGTCCCGTCC[A/G]CTGTAGGCCTGCATC | 71991 |
rs30028471 | snp | A/C | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108160227 | GTTTATCCATAGATA[A/C]CTTTTTAAGGACTTA | 71991 |
rs30063403 | snp | A/G | 0.375 | 0.216506 | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108162517 | ACTCAGTTCTAAGAT[A/G]GGTGTTATTTTAAGA | 71991 |
rs33882969 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Ercc8, Gm32268 | Mm_Celera | 13:108167098 | TGTCTTACGGGGGGC[A/G]GGGGGGGGAGGGGGA | 71991 |
rs45752738 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108160909 | AAATGTTATCAGATC[A/G]ATATTCCAAATGTGG | 71991 |
rs45833684 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufaf2, Ercc8 | Mm_Celera | 13:108158654 | CACTGCCCGGCGTTT[C/T]CCGAGCCCCCCAGTA | 71991 |
rs45890567 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108161292 | GGCACACCACGCATC[A/G]GCACACCACGATATT | 71991 |
rs45891302 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108163868 | TAAGAATCTCAGAAA[A/T]GAGGTTATTAAACCT | 71991 |
rs45902010 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Ercc8 | Mm_Celera | 13:108169264 | GTGTGATCCTACTGT[A/G]GAAATCCATATCTTC | 71991 |
rs45905089 | snp | C/T | 0.32 | 0.24 | intron-variant, downstream-variant-500B | Ercc8 | Mm_Celera | 13:108178012 | ATATTACACAGAAAG[C/T]TACAATAGATTAAAG | 71991 |
rs45907310 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108164042 | AGGACTGGGCTGTAG[C/T]GCAGTGGTGTAGTGC | 71991 |
rs45928811 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Ercc8 | Mm_Celera | 13:108192219 | ACTGCTGGCTGGAAA[C/T]GAGTGCTTAGCTGGA | 71991 |
rs45970297 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Ercc8 | Mm_Celera | 13:108174333 | GCAGCTCGGAGCCCC[A/G]GCTGTTTCTACATGA | 71991 |
rs45973552 | snp | C/T | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108197307 | GTTTTCTGTGTTAGT[C/T]TTCACACAGTGACCA | 71991 |
rs45975152 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Ercc8 | Mm_Celera | 13:108193955 | AATTAGCAGCAATAC[A/C]GTTTCCAAACATTCT | 71991 |
rs46036108 | snp | A/G | 0.32 | 0.24 | intron-variant | Ercc8 | Mm_Celera | 13:108174538 | TGTCATGTTAGAATG[A/G]AACTCAGAAATGCAC | 71991 |
rs46052465 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc8 | Mm_Celera | 13:108172556 | TCTTGCCTTAACTTC[C/T]GGGATTTGTCATGTT | 71991 |
rs46055105 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Ercc8 | Mm_Celera | 13:108169064 | TACCACCTCCAAGAT[A/G]AAGGAAACCCACTGT | 71991 |
rs46074990 | snp | C/T | 0.345679 | 0.230967 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108199148 | TAATTTCTAAATAAA[C/T]ACATCACGCAAAGCT | 71991 |
rs46102855 | snp | A/C | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc8, Gm32268 | Mm_Celera | 13:108166874 | AACAGGGTGTAGTGA[A/C]TATGTAGGCAGTACT | 71991 |
rs46108433 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108194743 | GAAACTTGTTGCAAC[A/G]GTGGCATCATAATGC | 71991 |
rs46127629 | snp | A/G | 0.32 | 0.24 | intron-variant | Ercc8 | Mm_Celera | 13:108177176 | AAGATATTAAAGATG[A/G]ATTTGACCACAAAGG | 71991 |
rs46183355 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Ercc8 | Mm_Celera | 13:108178825 | AAGATGCTTTAGATG[G/T]GAACGACATATTCTC | 71991 |
rs46197457 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Ercc8 | Mm_Celera | 13:108171330 | TTTTGTCTTGGGGAT[A/T]GATATTAAGATGAAG | 71991 |
rs46239138 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Ercc8, Gm32268 | GRCm38.p3 | 13:108163129 | TGACTGCAAGGTCTG[A/T]GTGCTGTCAGCATGT | 71991 |
rs46248327 | snp | A/G | 0.165289 | 0.235211 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108194944 | TGTGAAACTCAGCAA[A/G]ATCCATGCAGGGATG | 71991 |
rs46267547 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc8 | Mm_Celera | 13:108176733 | GGAAAGAAGATCACA[C/T]ACACAAAAACCTGTA | 71991 |
rs46346281 | snp | C/G/T | 0.396694 | 0.202437 | intron-variant | Ercc8 | GRCm38.p3 | 13:108192363 | AGCAGCCTGTATCAC[C/G/T]GTGTGTTTTCTAGCT | 71991 |
rs46361015 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Ercc8 | Mm_Celera | 13:108192678 | TGAAATGATTTCCCA[A/C]CGATAAGAAAGTAGC | 71991 |
rs46361914 | snp | A/T | | | upstream-variant-2KB, intron-variant, downstream-variant-500B | Ndufaf2, Ercc8, Gm32268 | Mm_Celera | 13:108159118 | CTGTCACTCCAGGAG[A/T]GACCTGATGGCAGGC | 71991 |
rs46362757 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Ercc8 | Mm_Celera | 13:108176270 | GCTCTGATATAAAGT[A/T]CCCATCTATCCATTG | 71991 |
rs46403532 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Ercc8 | Mm_Celera | 13:108190825 | TTTCAATGCATGTGT[C/T]ACGTTGTCAAGCCAA | 71991 |
rs46427206 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc8 | Mm_Celera | 13:108179644 | AGTACCTGGGTCTCA[C/T]AGGGCAGTCATGAAA | 71991 |
rs46481624 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Ercc8, Gm32268 | Mm_Celera | 13:108167511 | TTCCATCATTCTTAG[C/T]ATGCTTCTGTGGTAA | 71991 |
rs46483245 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Ercc8 | Mm_Celera | 13:108182499 | TTCCTAACGTGGAAT[G/T]AATGAATCTTATGTA | 71991 |
rs46503922 | snp | C/T | 0.32 | 0.24 | intron-variant | Ercc8 | Mm_Celera | 13:108174563 | ATGCACATTTTTATC[C/T]GTCTCTGAGAAACAT | 71991 |
rs46552730 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Ercc8 | Mm_Celera | 13:108168994 | TGTGGAACAGTCCAC[A/C]GTTCTAATAATGATA | 71991 |
rs46566711 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108160862 | TTGTTGGAAAAGCAT[C/T]TATTCATTTGAAATC | 71991 |
rs46620970 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ercc8 | Mm_Celera | 13:108191180 | AGCTGAGTGTGCTTA[C/T]TCATTGCTGTAACCT | 71991 |
rs46667493 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Ercc8 | Mm_Celera | 13:108190948 | TTAAAAGACGTTAGA[G/T]TAGGTGACAGGAACA | 71991 |
rs46725382 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Ercc8 | Mm_Celera | 13:108169199 | ATGGGTACCAAATTT[A/G]GAGATGCCTAGATAT | 71991 |
rs46774760 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108196136 | acccagtgcctggac[C/T]tttcttccctcagat | 71991 |
rs46782104 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime | Ndufaf2, Ercc8 | Mm_Celera | 13:108158633 | ACGCCCACGCTAAGC[C/T]CCGCCCACTGCCCGG | 71991 |
rs46800985 | snp | C/T | 0.297521 | 0.245442 | intron-variant | Ercc8 | Mm_Celera | 13:108193267 | TATTAACCTTGTTAC[C/T]ATTTCTCTTGGAGTT | 71991 |
rs46934140 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Ercc8, Gm32268 | Mm_Celera | 13:108167803 | TTTGAGCCATTTACA[C/T]ACTTTCAACCCTAAT | 71991 |
rs46938180 | snp | C/T | | | intron-variant | Ercc8 | Mm_Celera | 13:108185635 | CAGAGAGGGCTAAGA[C/T]TCAGTTAAAATTACA | 71991 |
rs46992453 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime, nc-transcript-variant | Ercc8 | Mm_Celera | 13:108198703 | GCACTAATGTATACA[C/T]AGAGCTCTCCTGGTT | 71991 |
rs46992739 | snp | A/G | | | intron-variant | Ercc8 | GRCm38.p3 | 13:108189071 | TTCCCTGGGTAGTAA[A/G]TAACCCTGATAGACA | 71991 |
rs46998916 | snp | A/G | | | intron-variant | Ercc8, Gm32268 | Mm_Celera | 13:108161287 | GTCACGGCACACCAC[A/G]CATCGGCACACCACG | 71991 |