SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13459188 | snp | G/T | 0.410009 | 0.192086 | missense, upstream-variant-2KB | Maf1, Sharpin, Gm35339 | Mm_Celera | 15:76352871 | GAGCCAGGGTGGTGA[G/T]GATGAGAGTCCTCTG | 106025 |
rs13462857 | snp | C/G | 0.375 | 0.216506 | utr-variant-5-prime, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351596 | AAAGCCCGCGCCGCC[C/G]TCACCTCGGCACCGA | 106025 |
rs13467974 | snp | A/G | | | upstream-variant-2KB, synonymous-codon, intron-variant, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76350137 | TGGAGGTCCTGGAAC[A/G]TTCAGCGTGCACTTC | 106025 |
rs32098181 | snp | G/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351784 | TGGGGCTGGAGCGCC[G/T]CTCTTGGTGCACTGC | 106025 |
rs46331471 | snp | A/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351760 | GGGACTTGTAGTTCT[A/T]ATGCTGCTTGGGGCT | 106025 |
rs47330110 | snp | G/T | 0.132653 | 0.220748 | upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351258 | GAGTCCACCAATAAG[G/T]TTTCTCGTGGTCTGG | 106025 |
rs48077828 | snp | C/T | 0.46281 | 0.131194 | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351792 | GAGCGCCTCTCTTGG[C/T]GCACTGCCTCCTGGG | 106025 |
rs48111545 | snp | A/G | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76349440 | TTTATAACAGCGGCA[A/G]AATTACAGTTATTAA | 106025 |
rs50612152 | snp | A/T | 0.260355 | 0.249785 | upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351178 | GGGAGGCGGGTTCGT[A/T]AGCGAGTGCGAGACA | 106025 |
rs211971133 | snp | G/T | | | missense, utr-variant-5-prime, nc-transcript-variant | Sharpin | Mm_Celera | 15:76348417 | GCTGGGGCTGGGGCT[G/T]GGGCTGGGCTGCCAC | 106025 |
rs212169392 | snp | C/T | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76346916 | TTCTAAGTGCACTCA[C/T]TCTTCAGTAGACTCC | 106025 |
rs212479678 | snp | A/G | | | utr-variant-5-prime, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351618 | CGGCACCGACACTAA[A/G]CAACCCGTCTACCCT | 106025 |
rs215142802 | snp | A/G | | | intron-variant | Sharpin | Mm_Celera | 15:76348876 | CCAACAAGGTGGAAA[A/G]TGAGGACTGACACTC | 106025 |
rs216027641 | snp | A/G | | | upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351226 | GTAGAAGTGGAAGGT[A/G]AAGCCGAGTGGCGGA | 106025 |
rs220359663 | snp | A/G | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351847 | TGCTGGTACCTCTAG[A/G]CTTGCAGGGCAGCAA | 106025 |
rs220549316 | snp | C/T | | | intron-variant | Sharpin | Mm_Celera | 15:76347437 | TTCTTCCAATGCCCA[C/T]AGCTGCCCATATCTG | 106025 |
rs220735793 | snp | C/G | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76349961 | TCCTTCCTCTTGGAA[C/G]CCTTCCTAGGTGCCC | 106025 |
rs221726136 | snp | A/T | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76352299 | GTAAGGTGAGGAAGA[A/T]GAGCTCCATGGTGGA | 106025 |
rs222028187 | snp | C/T | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76349601 | GTGACTTTGGGTGAC[C/T]TCTCCAACTCCCAGT | 106025 |
rs222063679 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Sharpin | Mm_Celera | 15:76347046 | AACACAGGCTGGCTC[G/T]TATGTGTCTTTAATT | 106025 |
rs222605991 | snp | G/T | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76346978 | TGTTGGGCAGAACCT[G/T]GTTTCCTTGCTCTCA | 106025 |
rs227315826 | snp | A/G | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin, Gm35339 | Mm_Celera | 15:76353036 | GAACAGAAGGGCCCC[A/G]AGCCATGTGGTCCTT | 106025 |
rs227345801 | snp | G/T | | | upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351185 | GGGTTCGTTAGCGAG[G/T]GCGAGACAGACAAGC | 106025 |
rs228093407 | snp | C/G | | | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76350538 | AGGCCGCTCAGGGTC[C/G]GCTATCAATTGCAGC | 106025 |
rs228148290 | snp | A/G | | | synonymous-codon, downstream-variant-500B, nc-transcript-variant | Sharpin | Mm_Celera | 15:76347983 | CAAAACCGATGTGGC[A/G]TCTTCAACTGTGACT | 106025 |
rs228550844 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76350954 | CCGGTCACAAAAAGA[A/C]GGCAAGGATGAACTT | 106025 |
rs228996855 | snp | G/T | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin, Gm35339 | Mm_Celera | 15:76352582 | TCTGGGGATCAATCT[G/T]TCAGAGATCACTATC | 106025 |
rs230572660 | snp | C/T | | | synonymous-codon, nc-transcript-variant | Sharpin | GRCm38.p3 | 15:76347512 | GAGACTGGAACTGGA[C/T]GGCTGGAGGTCATGA | 106025 |
rs231906396 | in-del | -/CGACGTA | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351923 | CCATCCTACACACTT[-/CGACGTA]CGAAGTACGAATTAG | 106025 |
rs232029400 | in-del | -/C | | | intron-variant | Sharpin | Mm_Celera | 15:76347236 | CACTGTACCCCCTCA[-/C]CCCCCCCCCCAGACT | 106025 |
rs232296404 | in-del | -/A | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76346761 | CTGGCTGAAGCAGCT[-/A]AAAAATAATGGTGAT | 106025 |
rs234138981 | snp | C/G | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76346566 | ACCTAGTAGTCTACA[C/G]TGCAGCTACATAGTA | 106025 |
rs235468812 | snp | A/T | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76346927 | CTCACTCTTCAGTAG[A/T]CTCCTGGTTGTGGCT | 106025 |
rs235753366 | snp | A/G | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76349670 | CCAAGCAGGCACTGG[A/G]TATAAGCCTCATACT | 106025 |
rs237122668 | snp | A/G | | | intron-variant | Sharpin | Mm_Celera | 15:76348735 | TAAAGTGCTTTTCAT[A/G]CAGACATAGACCTGA | 106025 |
rs238839712 | snp | G/T | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76350327 | ACGGCTCTGAACTTT[G/T]CTCGCCTGTTATCTT | 106025 |
rs239073882 | snp | G/T | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76347000 | TTGCTCTCAGGGAGC[G/T]GGGCTAGTACAACTC | 106025 |
rs239649571 | snp | A/G | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351875 | CAATGCCAGGAGACC[A/G]CTGGCCTGCGCCAGC | 106025 |
rs241305494 | snp | A/C | | | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76350670 | CGCACCGCCGGCGGG[A/C]GGCGACATTTCTGAT | 106025 |
rs242250474 | snp | G/T | | | utr-variant-3-prime, nc-transcript-variant | Sharpin | GRCm38.p3 | 15:76347119 | TGTCCCCAACAAGCA[G/T]CAGTCCCCTGCAAAG | 106025 |
rs242676575 | snp | A/C | | | intron-variant | Sharpin | Mm_Celera | 15:76347438 | TCTTCCAATGCCCAC[A/C]GCTGCCCATATCTGG | 106025 |
rs242687578 | in-del | -/GT | | | intron-variant | Sharpin | Mm_Celera | 15:76348995 | CAGACACACACTCAC[-/GT]GTGTGCACACACACA | 106025 |
rs242954394 | snp | A/C | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin, Gm35339 | Mm_Celera | 15:76352591 | CAATCTGTCAGAGAT[A/C]ACTATCGTGGGCCTC | 106025 |
rs243817891 | in-del | -/TG | | | intron-variant | Sharpin | Mm_Celera | 15:76347224 | CTGTTTATTCTACAC[-/TG]TACCCCCTCACCCCC | 106025 |
rs244989000 | snp | C/T | | | missense, nc-transcript-variant | Sharpin | Mm_Celera | 15:76347525 | GACGGCTGGAGGTCA[C/T]GAGGCAGCCCCAGTG | 106025 |
rs245357732 | snp | A/C | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76350035 | CATATTCAAATAAGC[A/C]TTTATTTCACAACAC | 106025 |
rs246551908 | snp | C/T | | | upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351200 | TGCGAGACAGACAAG[C/T]TATGCAGCCAGTAGA | 106025 |
rs247310484 | snp | A/C | | | intron-variant | Sharpin | Mm_Celera | 15:76348258 | ACAGCTATCACAACT[A/C]GACACCAGCCACAAA | 106025 |
rs247343822 | snp | C/G | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76346608 | AATTGACAGTCACTA[C/G]ATCCATGAAGGATCT | 106025 |
rs250636110 | snp | A/G | | | intron-variant | Sharpin | Mm_Celera | 15:76348825 | GTGTTCATATGGTGA[A/G]TGAGTTGGGGGTAGA | 106025 |
rs250782488 | snp | A/G | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76352331 | TCAAGGTTAGCTCGA[A/G]CTGCAAACAGTACTC | 106025 |
rs252288074 | snp | A/C | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351884 | GAGACCACTGGCCTG[A/C]GCCAGCAGAGGTGGT | 106025 |
rs252957674 | snp | A/G | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76349486 | AAATGTATGGCTGGG[A/G]GCCATACTGTATTAA | 106025 |
rs252997100 | snp | C/T | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76347028 | CTCCACATCCAAGAA[C/T]AGAACACAGGCTGGC | 106025 |
rs254202691 | in-del | -/TCTC | | | intron-variant | Sharpin | Mm_Celera | 15:76349253 | GCTAAGGTACCCAGG[-/TCTC]TCTCATGTCAGGCTC | 106025 |
rs255116848 | snp | C/T | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76351091 | GGCTCTTCGTAACCG[C/T]GGACCACTCTAGGAA | 106025 |
rs257112826 | in-del | -/CC | | | intron-variant | Sharpin | Mm_Celera | 15:76347235 | CACTGTACCCCCTCA[-/CC]CCCCCCCCCCCAGAC | 106025 |
rs257410982 | snp | C/T | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76350043 | AATAAGCATTTATTT[C/T]ACAACACTGACCATT | 106025 |
rs257797931 | snp | C/G | | | upstream-variant-2KB, synonymous-codon, utr-variant-5-prime, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76350493 | CACCGCCCCAGGCTC[C/G]GTGCCTAACAGTCCT | 106025 |
rs257836263 | snp | A/G | | | intron-variant, downstream-variant-500B | Sharpin | Mm_Celera | 15:76347847 | TGAGGGCTAGGCAGC[A/G]TCACTCACCCAGAAT | 106025 |
rs258425140 | in-del | -/ATG | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76351974 | AGAATTGAAGAATTC[-/ATG]GGTTTCCTCCTCTTG | 106025 |
rs261306238 | snp | A/G | | | utr-variant-5-prime, intron-variant, upstream-variant-2KB | Maf1, Sharpin | Mm_Celera | 15:76352434 | GGTAGTGCTGCCCTA[A/G]TCCCACTGGCACAAG | 106025 |
rs261507859 | snp | C/T | | | utr-variant-3-prime, nc-transcript-variant | Sharpin | Mm_Celera | 15:76347171 | CTGTGACAGGAGGGC[C/T]ATATTCTCTGTAACC | 106025 |
rs261602317 | snp | A/G | | | downstream-variant-500B | Sharpin | Mm_Celera | 15:76346954 | GGCTTGGGGAATCCC[A/G]CCAGCTACTGTTGGG | 106025 |
rs264350245 | in-del | -/ACCGGTC | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76350931 | GAGACAGTGTCACAG[-/ACCGGTC]ACCGGTCACAAAAAG | 106025 |
rs264366308 | snp | A/G | | | upstream-variant-2KB, intron-variant | Maf1, Sharpin | Mm_Celera | 15:76349915 | CTTGTCTGGTACTGG[A/G]GTCAGCTCTTGAACC | 106025 |
rs264547757 | snp | A/G | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | Maf1, Sharpin | Mm_Celera | 15:76350917 | TTTCAGCAGGACCCG[A/G]GACAGTGTCACAGAC | 106025 |
rs265174324 | snp | A/G | | | synonymous-codon, nc-transcript-variant | Sharpin | Mm_Celera | 15:76347500 | AGAGGGACTTGGGAG[A/G]CTGGAACTGGACGGC | 106025 |
rs584068812 | snp | A/G | | | downstream-variant-500B | Sharpin | GRCm38.p3 | 15:76346907 | GGGACTTGATTCTAA[A/G]TGCACTCACTCTTCA | 106025 |
rs586757235 | snp | C/T | | | upstream-variant-2KB | Maf1, Sharpin | GRCm38.p3 | 15:76351135 | TGGGGGCGGGGCGGG[C/T]ATGGTTCTAACCAAT | 106025 |
rs587501302 | snp | A/G | | | utr-variant-3-prime, nc-transcript-variant | Sharpin | GRCm38.p3 | 15:76347076 | TACTAGCTTGTATGT[A/G]GCCCCTGTTGTTTAA | 106025 |