SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6152164 | snp | A/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14108737 | gccaatcctattcaa[A/G]ctggcacaatcttca | 20844 |
rs6153295 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Stam | Mm_Celera | 2:14108984 | AAACATGTCATTTTT[A/T]AGTTGGCTAATGATA | 20844 |
rs6164823 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | Stam | Mm_Celera | 2:14148673 | TGAAGAtgatgatgg[A/G]cacccttaatctcag | 20844 |
rs6165274 | snp | A/C | 0.5 | 0 | intron-variant, utr-variant-3-prime | Stam | Mm_Celera | 2:14148721 | aggcggagctcggtg[A/C]gtttgaggccagcct | 20844 |
rs6165416 | snp | A/G | 0.5 | 0 | intron-variant, utr-variant-3-prime | Stam | Mm_Celera | 2:14148805 | aaaaaCCATAACAGC[A/G]GTCTATAATTTGATA | 20844 |
rs6167616 | snp | C/T | 0.5 | 0 | utr-variant-3-prime | Stam | Mm_Celera | 2:14149199 | TCAATAAATCAGCAT[C/T]GTTCATTTCCAGTAT | 20844 |
rs6168013 | snp | A/G | 0.5 | 0 | downstream-variant-500B | Stam | Mm_Celera | 2:14149219 | ATTTCCAGTATAGAG[A/G]TCTTTCATGGGTGAC | 20844 |
rs6190878 | snp | C/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14104653 | AAAAATATCCTATGG[C/G]TGAGGATATAGCTTA | 20844 |
rs6225033 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14113030 | cagcttttcttaatg[C/T]ttaggttttttaaaa | 20844 |
rs6225538 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14113105 | tctaggaaatatttt[C/T]tcccattcATGGTAA | 20844 |
rs6261917 | snp | A/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090033 | ACTATTAGTGAGTAG[A/G]AGCATTTTGTATTAC | 20844 |
rs6275454 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090139 | TTATTTGTCAAAACA[C/T]TTGATATTCTAATTT | 20844 |
rs6276150 | snp | C/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090334 | CCTGTGTAACATCTT[C/G]ATTTCCATGGTTGTA | 20844 |
rs6276530 | snp | A/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090368 | GTCTACATTCCTGAC[A/T]ACAAATATGTACTGT | 20844 |
rs6276624 | snp | A/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090421 | ACTGTGACCCTTCAG[A/G]ATACTAGTATAGTGT | 20844 |
rs6277111 | snp | C/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090499 | CTGTAAATTGCAATA[C/G]CTNAACTCAATTGTA | 20844 |
rs6277112 | snp | C/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090502 | TAAATTGCAATANCT[C/G]AACTCAATTGTAAAT | 20844 |
rs6277565 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14090559 | CTTTTTACATTAGTA[C/T]AGAAGCTTCTAATTG | 20844 |
rs6289221 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Stam | Mm_Celera | 2:14128421 | CTTTGAAGTGGAAAG[C/T]CTTCCAGATTGGGTG | 20844 |
rs6289867 | snp | A/G | 0.359862 | 0.224567 | synonymous-codon, nc-transcript-variant | Stam | Mm_Celera | 2:14128572 | AGCAAAAGCAAGCCC[A/G]GCTCTCGTAGCCAAG | 20844 |
rs6290374 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Stam | Mm_Celera | 2:14128649 | AAGGTGAGTGAGTTT[G/T]CGAATTCTGGAATGG | 20844 |
rs6290410 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Stam | Mm_Celera | 2:14128667 | AATTCTGGAATGGGA[A/G]CGAAGAAGACAGGTC | 20844 |
rs6290488 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Stam | Mm_Celera | 2:14128708 | GTTTACAGAAAAAAG[A/G]ATTGTCTTCAGATAA | 20844 |
rs6290894 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14128726 | TGTCTTCAGATAAAG[C/T]AGGGCCGCTTCATTT | 20844 |
rs6291501 | snp | A/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14128876 | ACTGCTAATGGTTTG[A/T]TATTATATGAGGGTA | 20844 |
rs6360319 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14132385 | gattttaaaggtgtg[C/T]gtcaccactgnctgg | 20844 |
rs6360352 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14132396 | tgtgngtcaccactg[C/T]ctggcTAAGAATTTT | 20844 |
rs6361440 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14132577 | acattgaatggttaa[C/T]ggctacctgtaagtc | 20844 |
rs6361477 | snp | A/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14132602 | taagtctggggatct[A/G]ttgcctttgcccttc | 20844 |
rs6396308 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14141267 | gattcccagctctct[C/T]gtaaatgccagttgg | 20844 |
rs6410669 | snp | A/C | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14141555 | TAAAAAGTGCCTTTT[A/C]TAAAATTCCAGTNGA | 20844 |
rs6410685 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Stam | Mm_Celera | 2:14141568 | TTNTAAAATTCCAGT[G/T]GATAGAANTAACATG | 20844 |
rs6410703 | snp | G/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14141576 | TTCCAGTNGATAGAA[G/T]TAACATGTAAAGGAA | 20844 |
rs6411329 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14141696 | TTTCCGTATCATCTC[C/T]TNTAGGTATATCCAG | 20844 |
rs6411330 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14141698 | TCCGTATCATCTCNT[A/G]TAGGTATATCCAGGG | 20844 |
rs6413013 | snp | A/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14108651 | atgaaagctacatct[A/G]ntccatcaangcntc | 20844 |
rs6413015 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14108652 | tgaaagctacatctn[C/T]tccatcaangcntca | 20844 |
rs6413028 | snp | A/G | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14108661 | catctnntccatcaa[A/G]gcntcacctaatagc | 20844 |
rs6413041 | snp | C/T | 0.5 | 0 | intron-variant | Stam | Mm_Celera | 2:14108664 | ctnntccatcaangc[C/T]tcacctaatagcacc | 20844 |
rs27153019 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Stam | Mm_Celera | 2:14144175 | CTGTGAGTCAGTGAG[A/C]ATCCGCCCGGCCTGC | 20844 |
rs27153020 | snp | C/G | 0.132653 | 0.220748 | missense | Stam | Mm_Celera | 2:14141857 | TCTTCCTAGTCAGCA[C/G]ACCCAGGCTTCTTAC | 20844 |
rs27153021 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Stam | Mm_Celera | 2:14141836 | TCCATCCTCTGCAAA[C/T]CAAGCTCTTCCTAGT | 20844 |
rs27153022 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Stam | Mm_Celera | 2:14141478 | CATACACATTCATGT[A/G]AACATACATGTACTT | 20844 |
rs27153023 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14140796 | TACTTACAACAGAGT[G/T]TGTGCACCTTAATCT | 20844 |
rs27153024 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14139403 | GCATTTAATGAAATC[A/G]AAGGTGCTTGGTTTC | 20844 |
rs27153025 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14138874 | TCTGCTGATCACTTT[A/C]GTTATTTTGATGATT | 20844 |
rs27153026 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14138790 | GTAAAGTCAAGGGCT[A/C]CAGCATGGGATCTTT | 20844 |
rs27153027 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14138703 | CTACACAGTTGTGCT[C/T]ACCAGGCAGCATTAC | 20844 |
rs27153028 | snp | A/G/T | 0.244898 | 0.249948 | intron-variant, downstream-variant-500B | Stam | Mm_Celera | 2:14138651 | CCTTTCTTGAAAAGC[A/G/T]GGCTTCCCATAGGCC | 20844 |
rs27153029 | snp | C/T | 0.124444 | 0.216185 | intron-variant, downstream-variant-500B | Stam | Mm_Celera | 2:14138603 | TATGCATTGTTTTTA[C/T]CTTGCTCTGAGTGAG | 20844 |
rs27153030 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14137375 | AATGGAAAACTAACC[A/T]TCCTAACTATGAATT | 20844 |
rs27153031 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14137234 | TTGTGGAGATTATGC[C/G]CTGTAAGTTTAAATG | 20844 |
rs27153032 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14137082 | GGTGGAACAGCTGTC[A/T]TAATCTCTGCCAGAG | 20844 |
rs27153033 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14136859 | TGTGGGTATGTTTTG[C/T]AACTGCCTTTTTTAG | 20844 |
rs27153034 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Stam | Mm_Celera | 2:14135324 | CAGGACTTCATTTCT[A/T]GTAATAATTCCTGAA | 20844 |
rs27153035 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14135259 | AGAGATTGGGTAGTC[C/T]TCTGCTTAATTTCTG | 20844 |
rs27153036 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14135197 | TTTGAAGTACCACTA[A/C]ATTCGTTTATATATT | 20844 |
rs27153037 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14133990 | AATGTTTCACCTGTA[A/C]GTAAATGAACCTAGA | 20844 |
rs27153038 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Stam | Mm_Celera | 2:14132839 | TTTTCAGTGTCAGCT[A/G]TTGGCAAGCTTAGAA | 20844 |
rs27153039 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14131316 | TATGAAGGAGTGGTG[C/T]TACACAGCCAAGTGA | 20844 |
rs27153040 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14131140 | ACTTTTCAGTCTGTT[C/G]GTAGATGGTAGATTA | 20844 |
rs27153041 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14130672 | ACTAAAATCCACATT[C/T]GAAACTCTGCTGTAT | 20844 |
rs27153042 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14130448 | GTCAAAGCTGGAAAG[C/G]AGAAGTGTATAAGGC | 20844 |
rs27153043 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stam | Mm_Celera | 2:14129612 | CATGATTTTGTATGT[A/G]AAGTGAATCATAAAG | 20844 |
rs27153044 | snp | C/T | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant | Stam | Mm_Celera | 2:14129091 | AGGCAGGAAAGTCCG[C/T]GCCGTGTACGATTTT | 20844 |
rs27153045 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Stam | Mm_Celera | 2:14129031 | AGCCCCCGTGTCCAC[A/G]CTGTACCCCAGCACA | 20844 |
rs27153046 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14128047 | ATTAGCCCATGTTTT[C/T]ATCTGCACATTGTTT | 20844 |
rs27153047 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127945 | ATTGGCAAAATAGGC[C/T]GCATTCTGATCTGCA | 20844 |
rs27153048 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127898 | CCTGCTCACAATCAC[C/T]GTCAGCTTCTGGTCT | 20844 |
rs27153049 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127881 | AACAAATGCGGGCCA[C/T]GCCTGCTCACAATCA | 20844 |
rs27153050 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127820 | CACAGCAGGAAACAA[C/T]CACAAAGTGATGGAC | 20844 |
rs27153051 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14127743 | GCTGAACTGAGGGCT[C/T]AGGCATGGTTCATGG | 20844 |
rs27153052 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127723 | TACCAGAGATTAACA[A/C]GGGTGCTGAACTGAG | 20844 |
rs27153053 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127695 | GCTCCCTTGTTACAA[A/G]TCCTTGTTTAAGTAC | 20844 |
rs27153054 | snp | C/T | 0.32 | 0.24 | intron-variant | Stam | Mm_Celera | 2:14127676 | GTTTAGTTGCCCATC[C/T]TATGCTCCCTTGTTA | 20844 |
rs27153055 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127449 | CTGCTTTGAACCAAG[A/G]GTGATCCTCCTCATC | 20844 |
rs27153056 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14127278 | TTACTCTGTTCATTT[C/T]ACTTTTTAAATTGAT | 20844 |
rs27153057 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14127044 | GACTGTTTGCCATGC[A/C]CTACACTCAACATAT | 20844 |
rs27153058 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14126741 | TTGCCTCTCAGCTGG[C/T]AGGGTTTCTTCAAAG | 20844 |
rs27153059 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14126667 | GCTAATGGCTCTCAA[C/T]GGTACGAACTGAAGA | 20844 |
rs27153060 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14126336 | TCTATGCAAAGCTTG[A/T]CATTAGAAACTGTAA | 20844 |
rs27153061 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14125898 | CATTCACTAGATGTG[C/G]TTGTGTTTAGATCAG | 20844 |
rs27153062 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stam | Mm_Celera | 2:14118759 | TTGGTACCAGAAACA[A/G]TGTTTATCAAAGAGT | 20844 |
rs27153063 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stam | Mm_Celera | 2:14118547 | CCCAGGCCAGTCGGA[A/G]TAAAGACCTAGAAAG | 20844 |
rs27153064 | snp | C/G | 0.32 | 0.24 | intron-variant | Stam | Mm_Celera | 2:14118445 | GAGGCTATGAACAAA[C/G]CAGCCCTTCTGTGAA | 20844 |
rs27153065 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Stam | Mm_Celera | 2:14118324 | TTCTATTTTGGGTAA[C/G]CATCTTTAGGGATAT | 20844 |
rs27153066 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14118212 | ACTGACTGCTGCAGG[G/T]GTAGCTTTCTTCCTG | 20844 |
rs27153067 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14118170 | AGAGCTAAGTAGAGC[C/G]TTAGTCTTCTGCCTT | 20844 |
rs27153068 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14116917 | CTATGTTGGGCCAGA[C/T]CTTTAGAAGGAGTTG | 20844 |
rs27153069 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14116786 | TTTTGTACCCATGAA[A/G]GCATTTCCCTAATGT | 20844 |
rs27153070 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14116200 | AGACTGTAAGAACTG[C/T]GTTTCCTTGAAAAGA | 20844 |
rs27153071 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14116156 | CCATTTCAAATTCCA[A/G]AGAACGTTTGTGTAT | 20844 |
rs27153072 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14115759 | GTATAATACCTTCCC[A/T]TTTGTACACTGATTG | 20844 |
rs27153073 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14115474 | GAAAAGCACCTGTCA[C/T]TACCCAAAATATGGG | 20844 |
rs27153074 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14115371 | CTGTTGCATCTCCTT[A/G]GACCTGTCTGCTTTT | 20844 |
rs27153075 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14115258 | TCATTAGGAAGACCA[C/G]GGTCACTCCTGCATT | 20844 |
rs27153076 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14114749 | CGTGCACATCCGCTT[A/T]TTTTTTTTTTCATTT | 20844 |
rs27153077 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14114602 | TCTGACTTGTTTCCT[C/T]TTTGTGAATTATTAT | 20844 |
rs27153078 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stam | Mm_Celera | 2:14112219 | ATTTGTTCCGGTCCC[C/T]GTTTTCTCCATCCTC | 20844 |
rs27153079 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Stam | Mm_Celera | 2:14112112 | GTTCAGAATCTTGCC[A/G]TGCAAGGTATCCCTC | 20844 |