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 | 102638882 |
rs13462858 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76354080 | CCCATGCTGTGGCTG[G/T]ATTAAACAGCACGGG | 102638882 |
rs32409698 | snp | C/T | 0.5 | 0 | intron-variant | Gm35339 | Mm_Celera | 15:76363475 | CTCCCCTGTCTCCCC[C/T]ACCCCCACCCCCAAC | 102638882 |
rs45845677 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76353989 | TGACACCGTCCTGGC[A/G]CTGCCCAAGGCTATA | 102638882 |
rs46094393 | snp | A/G | 0.231111 | 0.249285 | intron-variant, utr-variant-3-prime | Gm35339 | Mm_Celera | 15:76358460 | AAATAGGCATAGGCC[A/G]ACCACCGATCTCCAC | 102638882 |
rs46206701 | snp | G/T | 0.132653 | 0.220748 | synonymous-codon | Gm35339 | Mm_Celera | 15:76361238 | GTTGCCTGACATCAC[G/T]GGTAACCTCCGAATC | 102638882 |
rs46455368 | snp | C/G | 0.124444 | 0.216185 | splice-donor-variant, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76358631 | GGGTCTGACCTGATG[C/G]TAGGTATGAAATCAG | 102638882 |
rs46787577 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Gm35339 | Mm_Celera | 15:76361350 | CACCTCCACGTATCC[C/T]GACTTAGTCCCAGAA | 102638882 |
rs46912452 | snp | C/T | 0.124444 | 0.216185 | intron-variant, stop-gained | Gm35339 | Mm_Celera | 15:76360141 | CTCTTCCTAGTTTCC[C/T]AAGCTAAACTGCCCA | 102638882 |
rs47833967 | snp | C/T | | | missense, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76358944 | ATTCCACCCACCTAC[C/T]GGAGGGTGCATAGCC | 102638882 |
rs48380182 | snp | C/G | 0.152778 | 0.230321 | missense, intron-variant | Gm35339 | Mm_Celera | 15:76357424 | AGCCAAGGAGAAGCC[C/G]GTGCCCTCACCCTCA | 102638882 |
rs48662147 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Gm35339 | Mm_Celera | 15:76363440 | TAAGTAGACGCAGGC[A/G]TAAGAGCTGGACCCT | 102638882 |
rs49441528 | snp | C/G | 0.142012 | 0.225474 | synonymous-codon | Gm35339 | Mm_Celera | 15:76363253 | AAGGCCCAATGCTGT[C/G]CTGCGGCCGCGCCGG | 102638882 |
rs49885607 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Gm35339 | Mm_Celera | 15:76361620 | TTCCTGTCCCAGGCA[A/G]GAGCTCAAGAAGCTG | 102638882 |
rs49918178 | snp | G/T | 0.152778 | 0.230321 | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76364167 | AAGTGGGTCTCAGCA[G/T]AATATTCTCTGCAGT | 102638882 |
rs50356037 | snp | A/G | 0.244898 | 0.249948 | missense | Gm35339 | Mm_Celera | 15:76363714 | AAGATACATACCCTG[A/G]TGCCTTCAGTTGACC | 102638882 |
rs51314694 | snp | A/T | 0.132653 | 0.220748 | synonymous-codon, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76353350 | TTTCAGCTATAACCC[A/T]GATCTAGACTCCGAC | 102638882 |
rs51422423 | snp | A/C | 0.132653 | 0.220748 | missense, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76360727 | GAAGCCAGACACAGA[A/C]GTAGGCACTCTAGGT | 102638882 |
rs52291421 | snp | A/G | 0.32 | 0.24 | intron-variant | Gm35339 | Mm_Celera | 15:76361891 | CCCGAGTTTTTGAAA[A/G]CAGAATCTTCCTTCC | 102638882 |
rs52531626 | snp | A/G | 0.142012 | 0.225474 | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76363907 | TGTGGGCATGCTTGT[A/G]GAGGCCAAAAATTGC | 102638882 |
rs52704950 | snp | A/G | | | synonymous-codon | Gm35339 | Mm_Celera | 15:76363187 | ggaggaggaggagga[A/G]gaggaggaagaggag | 102638882 |
rs108461097 | snp | A/C | | | intron-variant | Gm35339 | Mm_Celera | 15:76363483 | TCTCCCCCACCCCCA[A/C]CCCCAACCTCAGCCT | 102638882 |
rs212183811 | snp | C/G | | | synonymous-codon, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76353595 | ATCCAGTGGCTCCAC[C/G]TACACACCCTCAGAG | 102638882 |
rs212626193 | in-del | -/AGGAGA | | | cds-indel | Gm35339 | Mm_Celera | 15:76363120 | GATCATCGATGGGAG[-/AGGAGA]AGGAGGAGGAGGGGA | 102638882 |
rs213242060 | snp | C/T | | | intron-variant | Gm35339 | Mm_Celera | 15:76358161 | ACTATGGGGTGTTAC[C/T]ACATTCTCAATCCAG | 102638882 |
rs213457986 | snp | A/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76362420 | TGGTTGTGAGCCACC[A/G]TGTGGTTGCTAGGAT | 102638882 |
rs213551377 | snp | A/G | | | synonymous-codon | Gm35339 | Mm_Celera | 15:76361416 | CTGAGTGCAGGACCC[A/G]ACGCAGAAGGAGTTT | 102638882 |
rs213677825 | snp | A/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76359747 | GCCTGAGCCAGGAGT[A/G]TGTCACCAGCGTTTG | 102638882 |
rs213812031 | snp | C/G | | | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76364248 | AAGGGCTTATGCTTC[C/G]CTCTTTCCTTCATTC | 102638882 |
rs214550599 | in-del | -/A | | | intron-variant | Gm35339 | Mm_Celera | 15:76361384 | ACCACGGTCCACCCC[-/A]CCCACCCCCCCTGCT | 102638882 |
rs214594528 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76355878 | ATTCCCCACCTCTAG[C/T]ATCATCTCAGATCTG | 102638882 |
rs214627656 | snp | C/T | | | intron-variant, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76353830 | TAAAGGCCTACTGTG[C/T]GCCAACTTCTGCCTA | 102638882 |
rs214815900 | snp | G/T | | | intron-variant, missense | Gm35339 | Mm_Celera | 15:76360060 | GGAGAGAATGTGTGC[G/T]TGCAGTCAGTGCTCA | 102638882 |
rs214959893 | snp | C/T | | | synonymous-codon | Gm35339 | Mm_Celera | 15:76358280 | GCCCTTCGGCTATTA[C/T]AAGAGATCAGAACCT | 102638882 |
rs215763249 | snp | A/G | | | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76363924 | AGGCCAAAAATTGCT[A/G]TCAAAGTGTTTATTG | 102638882 |
rs215886193 | snp | C/T | | | intron-variant | Gm35339 | Mm_Celera | 15:76362625 | GATGTTTCAAAGGTA[C/T]AGGTGCAAGAGTCCT | 102638882 |
rs216674805 | snp | A/T | | | intron-variant, missense, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76353334 | CTCTGCTGTTTTCTC[A/T]TTTCAGCTATAACCC | 102638882 |
rs216960585 | snp | A/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76357886 | CTGCGTCCTGGAAAC[A/G]AAGCTCTATCTGCTT | 102638882 |
rs216993792 | snp | C/G | | | synonymous-codon, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76356250 | AGGAGAGGTAACTCT[C/G]GGTTGCTGGACCGAA | 102638882 |
rs217265399 | in-del | -/C | | | intron-variant, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76353744 | TGGCTGTGGCCATGG[-/C]ACTATCCTCGGGAGC | 102638882 |
rs218208697 | in-del | -/CCTT | | | intron-variant | Gm35339 | Mm_Celera | 15:76361948 | CTTCCTTCCTTCCTC[-/CCTT]CCTTCCTTCCTTTTG | 102638882 |
rs218898313 | snp | C/T | | | intron-variant, synonymous-codon | Gm35339 | Mm_Celera | 15:76360221 | CCATGGTTCTGAAGA[C/T]GCTCCCTGGTAATGT | 102638882 |
rs219739943 | snp | A/G | | | missense | Gm35339 | Mm_Celera | 15:76363264 | CTGTGCTGCGGCCGC[A/G]CCGGGAACGCTGGTG | 102638882 |
rs219772633 | snp | A/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76361879 | CCCCGAGTTACCCCC[A/G]AGTTTTTGAAAACAG | 102638882 |
rs220615169 | snp | C/T | | | synonymous-codon, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76356508 | GGTCCACCTGGTGTC[C/T]GCTACTACAGGACGA | 102638882 |
rs220782493 | snp | A/G | | | missense, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76360543 | AGCAGTGGTCAAGGC[A/G]CCGAAAGCATTCTTC | 102638882 |
rs220836499 | snp | C/T | | | missense, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76356689 | CGTCCACCTCCACCT[C/T]CAGCGCCGCAGCCCT | 102638882 |
rs220868574 | snp | A/G | | | downstream-variant-500B, missense, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76354569 | GGCTAATAGAAACAG[A/G]CAACCTCTATTCATC | 102638882 |
rs221192488 | snp | C/T | | | downstream-variant-500B, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76354427 | GTGGGGCGGGGCCTG[C/T]GTCGTGGGGCGGGGC | 102638882 |
rs221429815 | snp | C/G | | | missense | Gm35339 | Mm_Celera | 15:76361711 | GTTGAGGACTTGAAA[C/G]TTGAATCCAAGGCCA | 102638882 |
rs221927884 | in-del | -/CCCAGC | | | intron-variant | Gm35339 | Mm_Celera | 15:76357606 | AGTGGCTAGAGGGCA[-/CCCAGC]CCCAGCGGGGCTCTT | 102638882 |
rs222069841 | snp | A/C | | | missense, utr-variant-3-prime | Gm35339 | Mm_Celera | 15:76360351 | CCCAACTCTGTGGTA[A/C]TGCGGCAAATGTGGT | 102638882 |
rs222101652 | snp | G/T | | | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76364353 | TTTTGTTTTGGTTTG[G/T]TTTTGGTTTTTTGTT | 102638882 |
rs222311441 | snp | A/G | | | utr-variant-3-prime, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76354194 | TTATTGGGCCTGTAC[A/G]CTCCAGCTCTAAGGG | 102638882 |
rs224104370 | in-del | -/ACGGACGGA | | | intron-variant | Gm35339 | Mm_Celera | 15:76357109 | CCTGGGGGGTGGGGG[-/ACGGACGGA]CTCCTGCACTATCCT | 102638882 |
rs224682502 | in-del | -/CCCTGATTCTACTGGT | | | intron-variant, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76355043 | CCTAGAGATACTGGG[-/CCCTGATTCTACTGGT]CCTTATGAGTTTCCC | 102638882 |
rs226057579 | snp | A/T | | | intron-variant, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76360753 | TAGGTCCTCATGGGG[A/T]GGGTGAGATTGGTGC | 102638882 |
rs226309486 | in-del | -/TGAG | | | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76364126 | GATGCTTCAGTTGTT[-/TGAG]TGTTTTCCTTTATGT | 102638882 |
rs226676212 | snp | A/C | | | synonymous-codon | Gm35339 | Mm_Celera | 15:76357287 | GCGCATCACTGCAGG[A/C]TTTGAGGATCCAGAG | 102638882 |
rs226744822 | snp | C/T | | | missense | Gm35339 | Mm_Celera | 15:76362850 | CTATGGAGCAGGTGA[C/T]GTCTATTGTATCCAT | 102638882 |
rs226948689 | snp | C/T | | | intron-variant, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76358643 | ATGGTAGGTATGAAA[C/T]CAGGCCCAGGCTCTG | 102638882 |
rs226987422 | snp | A/G | | | missense | Gm35339 | Mm_Celera | 15:76359154 | GCCATAGACCTGGAC[A/G]CATCAATCGACTACA | 102638882 |
rs227025006 | snp | C/T | | | synonymous-codon | Gm35339 | Mm_Celera | 15:76357761 | CTATGGAGACCTGGT[C/T]TTCTCACTAGGCTCC | 102638882 |
rs227315826 | snp | A/G | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin, Gm35339 | Mm_Celera | 15:76353036 | GAACAGAAGGGCCCC[A/G]AGCCATGTGGTCCTT | 102638882 |
rs227373585 | snp | C/T | | | intron-variant | Gm35339 | Mm_Celera | 15:76361795 | TGGGCCAAGGGCTGG[C/T]GGTTCACCTACTGGA | 102638882 |
rs227738901 | snp | A/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76362272 | TTGTTTTTGTTTTTC[A/G]AAACAGGGTTTCTCT | 102638882 |
rs227797584 | snp | C/T | | | synonymous-codon | Gm35339 | Mm_Celera | 15:76361208 | AGTGAACATTCTAAA[C/T]TCCCTGCTGAGGTTG | 102638882 |
rs228274986 | in-del | -/TTTG | | | intron-variant | Gm35339 | Mm_Celera | 15:76362197 | TGGTTTTTTTGTTTC[-/TTTG]TTTGTTTGTTTGTTT | 102638882 |
rs228329990 | snp | A/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76362231 | TGTTTTTTCGAGACA[A/G]GGTTTTTTGGTTTTT | 102638882 |
rs228875634 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76355100 | CTCGTGCCTCCATTG[C/T]TCACACGTACATCTG | 102638882 |
rs228996855 | snp | G/T | | | intron-variant, upstream-variant-2KB | Maf1, Sharpin, Gm35339 | Mm_Celera | 15:76352582 | TCTGGGGATCAATCT[G/T]TCAGAGATCACTATC | 102638882 |
rs229237178 | snp | C/T | | | downstream-variant-500B, intron-variant | Maf1, Gm35339 | Mm_Celera | 15:76354735 | TTCCTCAGGCTTTAT[C/T]CAGTCCTCAAGGTGT | 102638882 |
rs230488062 | in-del | -/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76358109 | AAAGGCCTCTTGGGA[-/G]TGTATGAGTTCTCTA | 102638882 |
rs230521694 | in-del | -/CC | | | frameshift-variant, intron-variant | Gm35339 | Mm_Celera | 15:76357462 | CTAATCTTAGTTCTG[-/CC]CCCTAGGTCTGTGCT | 102638882 |
rs230559514 | snp | G/T | | | intron-variant | Gm35339 | Mm_Celera | 15:76359864 | GCAAAGTTCAGTGGG[G/T]CCAGTTGTTCAAGAT | 102638882 |
rs230811577 | in-del | -/GCA | | | intron-variant | Gm35339 | Mm_Celera | 15:76358070 | CAGTGGCAGCCTGGG[-/GCA]GCAGGGTTTGCATAG | 102638882 |
rs231410229 | in-del | -/C | | | intron-variant | Gm35339 | Mm_Celera | 15:76363482 | TCTCCCCCACCCCCA[-/C]CCCCCAACCTCAGCC | 102638882 |
rs231991929 | snp | C/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76362483 | GCTCTTAACCACTGA[C/G]CCATCTCGCCAGCCC | 102638882 |
rs232027595 | snp | A/G | | | missense | Gm35339 | Mm_Celera | 15:76361466 | TGCTCCTGGCCTGCA[A/G]CCTGGACGTCCTTGA | 102638882 |
rs233075299 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76356019 | GTCAGGCTGGCAGCT[C/T]TTGCAGCCCTTCTCT | 102638882 |
rs233132381 | snp | G/T | | | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76364335 | TTTGCAGTCTGCTGG[G/T]TTTTTTGTTTTGGTT | 102638882 |
rs233618741 | snp | C/T | | | missense | Gm35339 | Mm_Celera | 15:76361736 | AGGCCACCATACGCA[C/T]CCAGTGTCAACAGAA | 102638882 |
rs233936207 | snp | A/G | | | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76363999 | CTCTACATAGTCATT[A/G]CTGGGGCTCGCTATG | 102638882 |
rs234059798 | snp | A/C | | | missense, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76360693 | CTTCCCAAACTTCGG[A/C]GACAGAGCCAGAACA | 102638882 |
rs234133965 | snp | C/T | | | missense | Gm35339 | Mm_Celera | 15:76357926 | TTGTGTCTGAAGGCC[C/T]CTGATGTGATCAGTG | 102638882 |
rs234461497 | snp | C/T | | | intron-variant, synonymous-codon | Gm35339 | Mm_Celera | 15:76360125 | ATCCCGCAAGACTAC[C/T]CTCTTCCTAGTTTCC | 102638882 |
rs234489235 | snp | C/T | | | synonymous-codon | Gm35339 | Mm_Celera | 15:76361257 | AACCTCCGAATCCGG[C/T]TGCAGGCCAAACTCT | 102638882 |
rs234729789 | snp | A/T | | | downstream-variant-500B | Gm35339 | Mm_Celera | 15:76364168 | AGTGGGTCTCAGCAG[A/T]ATATTCTCTGCAGTT | 102638882 |
rs235249816 | snp | A/G | | | intron-variant | Gm35339 | Mm_Celera | 15:76359225 | GGGGCTTTGGTGGTC[A/G]TGTTTTATTCTTACT | 102638882 |
rs235881300 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Gm35339 | Mm_Celera | 15:76356529 | TACAGGACGAACTGT[A/G]AGTTCACTGCTGTTG | 102638882 |
rs236049260 | snp | A/C | | | synonymous-codon, utr-variant-3-prime | Gm35339 | Mm_Celera | 15:76360302 | CCTCTACATCTAGCT[A/C]CGTTCTCGGCCCATC | 102638882 |
rs236230751 | in-del | -/CCCCCA | | | intron-variant | Gm35339 | GRCm38.p3 | 15:76363471 | AATGCTCCCCTGTCT[-/CCCCCA]CCCCCACCCCCAACC | 102638882 |
rs236369297 | snp | G/T | | | missense | Gm35339 | Mm_Celera | 15:76363222 | TACCTGTCTCACTCC[G/T]ACGACGCCACCAGCT | 102638882 |
rs237435362 | snp | C/G | | | synonymous-codon, upstream-variant-2KB | Maf1, Gm35339 | Mm_Celera | 15:76353700 | CAGGGCAGAGGAGAC[C/G]AGCACCATGGAGGAA | 102638882 |
rs237540666 | in-del | -/G | | | utr-variant-3-prime | Gm35339 | Mm_Celera | 15:76363731 | GCCTTCAGTTGACCT[-/G]GGGGACAGATAGCCA | 102638882 |
rs237608087 | snp | A/C | | | intron-variant | Gm35339 | Mm_Celera | 15:76358195 | TCTTTTCTCCTGGCT[A/C]CGTCTCACTCCAGCT | 102638882 |
rs237641023 | snp | C/T | | | intron-variant, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76359046 | CACCTTCTAACTCCT[C/T]GTATACCCTAGCTTC | 102638882 |
rs238389471 | snp | A/G | | | missense, downstream-variant-500B | Gm35339 | Mm_Celera | 15:76360384 | CAAGCAGAGGTCAGC[A/G]GTCTTGGCTCCCTAG | 102638882 |
rs238414395 | snp | C/T | | | intron-variant | Gm35339 | Mm_Celera | 15:76359242 | GTTTTATTCTTACTT[C/T]CTATCCCTCCCCAGG | 102638882 |
rs239502500 | snp | A/C | | | missense | Gm35339 | Mm_Celera | 15:76362667 | TCACTCCCCTCTAGG[A/C]GGATACCTTGGAGCA | 102638882 |