SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3710934 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gm15800 | GRCm38.p3 | 5:121230977 | GTAGACACAGAGGAA[A/G]CGAGTGAGGTGAGGA | 269700 |
rs3711671 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121231141 | GCACCACATAAAGCC[A/G]GATATATTGGGTATG | 269700 |
rs4138867 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121238879 | TCTCTCCTTCATACA[C/T]ACACACACATTCTAT | 269700 |
rs6184919 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121250457 | CCTGAGTTTCAGCTT[C/T]CCCACTAGAGATGGG | 269700 |
rs6270728 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121340243 | GGGTCACTCGAATTT[A/G]ACACATCGAACCCTA | 269700 |
rs6283686 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121340341 | ATGTCTCTAGCTCCC[C/T]CTCCCCTCTCCTAAG | 269700 |
rs6339756 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121304688 | GTGGCCCTCCAGGCA[C/T]AGTCCCAGACCCCGG | 269700 |
rs6341226 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121304944 | AGTCACACATGTGCT[A/G]TGCTGTTCTTAGCCT | 269700 |
rs6355471 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121305290 | CCAGAAGGCAGGCGA[A/G]TAGTTCTGAAGCTTg | 269700 |
rs6356331 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121305413 | ttacaaatcccttcc[C/T]cTTGTAGCTGTTATT | 269700 |
rs6360434 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121266498 | GCCACTTAAAGTACC[C/T]GTTGTGCTCAGTCTC | 269700 |
rs6361034 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121266630 | AGGTAACCTTACTGC[A/G]TGCATTGCAGTGGAT | 269700 |
rs6362095 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121266801 | TACCCTGCGGGTGGA[A/G]CANAGTGATGGCCAC | 269700 |
rs6362109 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121266804 | CCTGCGGGTGGANCA[C/T]AGTGATGGCCACGGG | 269700 |
rs29504547 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121236386 | ACTACTACACCCTCC[A/G]AGTTTGGAGAGCCTG | 269700 |
rs29506979 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121340942 | AGATAACCCAAATGT[A/G]GCCTGAGGTGTAAGA | 269700 |
rs29508118 | snp | A/C | 0.444444 | 0.157135 | upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121219186 | TGGAAAAAAAAAAGA[A/C]AAAACAAAACAAAAC | 269700 |
rs29508175 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gm15800 | GRCm38.p3 | 5:121230871 | CAGTAGTGTGGAGCT[G/T]CGCAGACTGCCGTGC | 269700 |
rs29509389 | snp | C/T | 0.375 | 0.216506 | intron-variant | Gm15800 | Mm_Celera | 5:121232804 | TCTAGGCAGGTGGTT[C/T]TGGGTTGTATAAGAA | 269700 |
rs29511756 | snp | G/T | 0.5 | 0 | upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121217685 | CTTAGATAATTTTTT[G/T]GGGGGGGGGGTTAAA | 269700 |
rs29524032 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Gm15800 | Mm_Celera | 5:121258974 | TTTCATTTTTTAATT[A/T]AAAAAAAGACCTAGT | 269700 |
rs29544661 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121341150 | GTATCAGATATCCTG[C/T]GTATGAGATATTTAC | 269700 |
rs29545923 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | Mm_Celera | 5:121231636 | ATTTATTCCTACAGG[C/T]TGAACTTCAGGAATT | 269700 |
rs29547469 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gm15800 | GRCm38.p3 | 5:121283252 | CTTCCTGAGGGCTGA[A/C]TGGATTTGGGGCTGA | 269700 |
rs29550615 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Gm15800 | GRCm38.p3 | 5:121309421 | TTGTTTGTTTGTTTG[G/T]TTGGTTGGTTGGTTT | 269700 |
rs29551098 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Gm15800 | GRCm38.p3 | 5:121229389 | TCCAGGGAAGATCAC[A/G]GGGTGTGCAGTTGTT | 269700 |
rs29552152 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gm15800 | GRCm38.p3 | 5:121242803 | TTAGGAACTCTTGAG[C/T]CTTGCTCCCAAGAGC | 269700 |
rs29560831 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Gm15800 | Mm_Celera | 5:121345844 | TAATCTCAAAAAAAA[A/C]CCCAAAAAACCTAGA | 269700 |
rs29576939 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gm15800 | GRCm38.p3 | 5:121228600 | GCTGAAGGAACTGTG[C/T]AACTGCTACTTTTTT | 269700 |
rs29580003 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime | Gm15800 | Mm_Celera | 5:121219521 | AATTGTTGATAGATA[C/T]TTTATTTTCATCAGA | 269700 |
rs29580687 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Gm15800 | Mm_Celera | 5:121243231 | CTTCCTTAATTAATT[A/T]ATTTATTTATATTTT | 269700 |
rs29583599 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121225252 | TGTAATTTGTCAAAT[C/T]GAGCATCAAACTTTT | 269700 |
rs29587319 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Gm15800 | Mm_Celera | 5:121233172 | TTTCTCTGTATAGCC[C/G]TGACTGTCCTGAAAC | 269700 |
rs29676305 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gm15800 | GRCm38.p3 | 5:121228327 | GTTGGCCAGGGTGGG[G/T]TGTTCTTTGCCTGTT | 269700 |
rs29678075 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Gm15800 | GRCm38.p3 | 5:121242951 | GTAGAGATAAAGAAT[A/C]CATTCCTGCAAGTTG | 269700 |
rs29678591 | snp | C/G | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121230688 | GCACTGGCATCTTCA[C/G]GTGCAGCCCAGCCAG | 269700 |
rs29682068 | snp | A/G | 0.5 | 0 | synonymous-codon | Gm15800 | GRCm38.p3 | 5:121350603 | CCAAGGGAGTCCAGG[A/G]CTGGAAGATTACTTC | 269700 |
rs29683665 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Gm15800 | GRCm38.p3 | 5:121229439 | ATCTGGAAACCTCTG[C/T]ATAGTTTCTGTGGTA | 269700 |
rs29685589 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121317297 | AGGTAACCACACGGC[A/G]GAAAATGACACACAC | 269700 |
rs29720346 | snp | A/G | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121258329 | GTGAAGTGGATGAAC[A/G]TAACCACGTCACAGA | 269700 |
rs29727955 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gm15800 | GRCm38.p3 | 5:121329785 | TGCAGGCTTGCATCT[G/T]CTGAGCTGTGTCCAG | 269700 |
rs29729060 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Gm15800 | GRCm38.p3 | 5:121253748 | GTTAAAGGTGTGAGC[C/T]ACATGCCCAGCACTG | 269700 |
rs32187704 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121230247 | TGGGCTTTTAGACTT[A/G]CACGGTCAAGGATCC | 269700 |
rs32187705 | snp | C/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121230679 | GGCTGTGCAGCACTG[C/G]CATCTTCACGTGCAG | 269700 |
rs32187706 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121230747 | AGCATCATTTGGAAT[A/G]GGGGCGGTTCTTCCC | 269700 |
rs32187707 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121231405 | ATTTAATAATAACAC[C/T]GTATGTGGGATGCAA | 269700 |
rs32187708 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121231450 | ACACCCATTATAATT[C/T]CAGTACTGGATCCTT | 269700 |
rs32187709 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121232296 | TATTCAGTGAAGATG[A/G]TTGTGATACAAGTCT | 269700 |
rs32187710 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121233724 | GTCAGTCAGCGTTTG[A/G]AAAACAGACAGCTAC | 269700 |
rs32187711 | snp | G/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121236826 | AACAAACTCTTGTAG[G/T]TTACGTATCCATATC | 269700 |
rs32187712 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121238245 | GGTATTTCTGATGTT[C/T]CTTGTTTCATTTCTG | 269700 |
rs32187713 | snp | A/G | | | intron-variant | Gm15800 | GRCm38.p3 | 5:121238313 | GCATCAACTCTTGCC[A/G]GAAATAAAACCCTTC | 269700 |
rs32188454 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121273512 | AGGTGGATGGGAAAC[A/G]CTTTGTAAGCACCCA | 269700 |
rs32188455 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121273833 | ACCACCTGCACAGGG[C/T]GGGTGCTGCAATGTG | 269700 |
rs32188456 | snp | G/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121274109 | AGATTCTGGATCTGA[G/T]CTAAAATTGGATTTG | 269700 |
rs32188457 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121275003 | GTTTATACCTCCATT[C/T]TCACTGTATGCCTTT | 269700 |
rs32188458 | snp | A/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121275734 | ACACACAAAACTGCA[A/T]CAGAATACATTTAGA | 269700 |
rs32188459 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121275865 | ACTAGTTCTGATCTA[A/C]ATGGATCTGTGAAAA | 269700 |
rs32188460 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121276352 | GAACCCCTTAGGGAG[C/T]GTTAGGCTATGAAGC | 269700 |
rs32188461 | snp | A/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121276440 | TGTCCTGAAGGAAGA[A/T]TATATTTGTTGAGGG | 269700 |
rs32188462 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121276593 | TCTCGTTTCTGTGGG[A/C]AAACTAAAAAAGAGA | 269700 |
rs32188463 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121276684 | AGACCTTGAACAATT[C/T]GAACAATTTTGTAGC | 269700 |
rs32188634 | snp | C/T | | | intron-variant | Gm15800 | GRCm38.p3 | 5:121238660 | GAGATTAAAAGTCAG[C/T]CATAATTTCTCCATT | 269700 |
rs32188635 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121239075 | CACATAAAATAAAAG[C/T]AAAACATTAAAAAAT | 269700 |
rs32188636 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121239496 | CAGTGCTTTATTGTG[A/C]CTCTAAACTTACTTA | 269700 |
rs32188637 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121239575 | TATGTGTCCCTTCAT[A/G]GAATATCTCTTGAGT | 269700 |
rs32188638 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121239965 | TCACACGTCACTCAT[A/G]AATGGAAGTGTTTAT | 269700 |
rs32188639 | snp | C/T | 0.5 | 0 | intron-variant | Gm15800 | GRCm38.p3 | 5:121240066 | AGTCAGCAGTTGTCA[C/T]CGCCTGCCACAGGCT | 269700 |
rs32188640 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121240121 | GGACTGGAGTGTGAT[A/G]TCTTTCTTCTCCATC | 269700 |
rs32188641 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Gm15800 | Mm_Celera | 5:121240507 | GGCCAGCTCAGAAAT[G/T]TATATCTTCTATAGT | 269700 |
rs32188642 | snp | A/C | | | intron-variant, upstream-variant-2KB | Gm15800 | GRCm38.p3 | 5:121245056 | GCTCATGCCCTGTCT[A/C]AGCACTAAGTCTCAG | 269700 |
rs32188643 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121245150 | TCTGAAGTGACAGAT[A/G]GATGTGATCTCTAAC | 269700 |
rs32188874 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121276826 | CACCTCCTGACTAGA[C/T]GTTATTCTGTATCTT | 269700 |
rs32188875 | snp | A/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121276851 | TATCTTCTGTCACTG[A/T]CCCTCAAAATAGAAG | 269700 |
rs32188876 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121277143 | AATAGGGTATCAATT[C/T]CCAGTTAAAGCTCAA | 269700 |
rs32188877 | snp | C/T | | | synonymous-codon, utr-variant-5-prime | Gm15800 | Mm_Celera | 5:121277691 | AAATACTAGCTGTGG[C/T]CTTCCTCTGAAAATG | 269700 |
rs32188878 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121278662 | TCTGTTACAGTTGCT[C/T]TCTGATAGCACAAAA | 269700 |
rs32188879 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121278676 | TCTCTGATAGCACAA[A/C]ATTATAATGGTTGAT | 269700 |
rs32188880 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121278749 | ATGGCACCCAGGCCA[C/T]GTGTTCTGCCGTTCT | 269700 |
rs32188881 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121278931 | GTCACCATGACTGTT[A/C]CCAAACTTTCCATTG | 269700 |
rs32188882 | snp | G/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121279039 | GAGAATGTGGCTGAT[G/T]CGTGAAATGCTTCCT | 269700 |
rs32188883 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121279074 | GGCCTGCTCCATGTT[A/G]CTCACCATGGCCATC | 269700 |
rs32189064 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Gm15800 | GRCm38.p3 | 5:121245411 | AGTGTCCCTGAATTG[A/G]TAATTAGCTGTGCGC | 269700 |
rs32189065 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121245431 | TAGCTGTGCGCGGTA[C/T]TCATTCTGGGCCCCT | 269700 |
rs32189066 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121245784 | GTGCCAGGTGCTCTG[C/T]GTTAGGATTTAGAAA | 269700 |
rs32189067 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121247599 | AGTAGTCAACTGCTC[A/G]GTGTTGCATGCTGAA | 269700 |
rs32189068 | snp | A/G | | | intron-variant | Gm15800 | Mm_Celera | 5:121248229 | GGAAAGGAGGCTGCA[A/G]GAGGTAGCTGGCAGA | 269700 |
rs32189069 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Gm15800 | GRCm38.p3 | 5:121248628 | GTTCTGAGTCTTCAG[A/G]TGTGTGTCACTGTGT | 269700 |
rs32189070 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121248775 | GAACACAGGGTCTTG[A/C]TTTAGCTGAGTGCTC | 269700 |
rs32189071 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121249741 | CATCTCACCAGCCCT[A/G]GAGAACCCTAAATAG | 269700 |
rs32189072 | snp | C/T | | | intron-variant, upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121249891 | ACTAACTTTCTGTTC[C/T]TGATCCAGGGCAGTA | 269700 |
rs32189073 | snp | A/G | | | intron-variant, upstream-variant-2KB | Gm15800 | Mm_Celera | 5:121250375 | AATGAGTTTGAATGA[A/G]CACGTTTCCAAGTGG | 269700 |
rs32189124 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121279616 | AGAGAAAGTAAGAGG[C/T]ACTGAGACTGTGGAG | 269700 |
rs32189125 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121279939 | GGAGAGCCATAGTTA[C/T]TTAGTGACTTTGTGG | 269700 |
rs32189126 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121280721 | GGCTGACAAGGCCAG[A/C]TGAAACCCTTCCTAC | 269700 |
rs32189127 | snp | G/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121280773 | CAAGGCTTCCTTCTG[G/T]GCTTTCTCTCTTTTG | 269700 |
rs32189128 | snp | A/C | | | intron-variant | Gm15800 | Mm_Celera | 5:121280799 | TTTTGACCTTCTAAT[A/C]TAGAAAAACACCTTC | 269700 |
rs32189129 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121281178 | GGATTGGGTAAGACA[C/T]GCCTGTTTCCTTGAA | 269700 |
rs32189130 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121281242 | GTCTCTGTGGCACTC[C/T]AGTGTTCTTAAAAGA | 269700 |
rs32189131 | snp | C/T | | | intron-variant | Gm15800 | Mm_Celera | 5:121281371 | TGTAAAATGATACCA[C/T]CACAGTCCTTTCCAT | 269700 |