SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6266997 | snp | G/T | 0.5 | 0 | intron-variant | Lats1 | Mm_Celera | 10:7689802 | AGTGAGCCCCTACTG[G/T]TTTTANTCCCTTGAA | 16798 |
rs6267001 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lats1 | Mm_Celera | 10:7689808 | CCCCTACTGNTTTTA[G/T]TCCCTTGAAGGGATG | 16798 |
rs29316295 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7709977 | TGGGCATGGAAGCCT[A/G]GCAAGGCAAGCACCG | 16798 |
rs29316808 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7708964 | TAGGCTAGCTGGACG[A/G]GAGTTCCAGGGGTCC | 16798 |
rs29317112 | snp | A/G | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7682028 | TTATTGTACCTGGGG[A/G]AAAAAGTCGAAGCGA | 16798 |
rs29317800 | snp | C/T | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7688256 | GCACCATGTGAGTGC[C/T]GGGAACTGAGGAAGC | 16798 |
rs29320421 | snp | C/T | 0.5 | 0 | downstream-variant-500B | Lats1 | Mm_Celera | 10:7716717 | CTCCATATATATATA[C/T]ACACACACACACACA | 16798 |
rs29323497 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7681862 | CGGGCCTCCCGTCGG[C/G]GTCCACCTTTGAAGC | 16798 |
rs29325080 | snp | A/C | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7701319 | GTGACAAATCAGTAT[A/C]CAGCGCTCGTGAAGC | 16798 |
rs29326111 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7680432 | TTTACTTTTTTGGTC[C/T]AACACAAAATAGAGT | 16798 |
rs29326208 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7681754 | GGCTCGGGACGACAG[C/T]CACCCCTCCCCGCTT | 16798 |
rs29327519 | snp | A/C/T | 0.5 | 0 | intron-variant | Lats1 | GRCm38.p3 | 10:7701394 | GAGCTGTCATGTGGG[A/C/T]GGTGGGAACTGGACA | 16798 |
rs29328599 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7684698 | AGATACAAAGGTAAG[A/G]GGAAGGCTGCCAGTT | 16798 |
rs29334871 | snp | C/T | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7694980 | TTTCAGACATAGAGA[C/T]AGAATTCCCTGCCTC | 16798 |
rs29334949 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7679937 | AGCAGCTCCAGCTCT[C/G]TGTGCTTAAAATATT | 16798 |
rs29338944 | snp | A/C | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | GRCm38.p3 | 10:7680603 | AATGGGAGTTTTGGC[A/C]CACACGCTGCGGCCT | 16798 |
rs29344334 | snp | G/T | 0.5 | 0 | intron-variant | Lats1 | Mm_Celera | 10:7708242 | TGTCTCTTTTCTGTG[G/T]AAATGTGTGTCCCTT | 16798 |
rs29344777 | snp | C/G | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7680610 | GTTTTGGCACACACG[C/G]TGCGGCCTAGAGATC | 16798 |
rs29346440 | snp | C/G | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7709029 | GCACTGGTTTTTACA[C/G]GGGTGTTAGGGGTCC | 16798 |
rs29346919 | snp | A/T | 0.32 | 0.24 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7679898 | CTGCACCCTGGCTTG[A/T]GCGGTGACTTAGCCC | 16798 |
rs29348424 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7680236 | CTGGGCTTCATGGAG[C/T]AGGCTTGTTATCTCA | 16798 |
rs29349270 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Lats1 | Mm_Celera | 10:7704946 | CCCCCTCTTCTTCCC[C/T]CTCCCCCTTGAAGCA | 16798 |
rs29350957 | snp | A/G | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7681810 | TTTTTTTCACGCAAG[A/G]TTGCACCAAACCGGC | 16798 |
rs29351737 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lats1 | Mm_Celera | 10:7704053 | CATATGCTCAGAATG[C/T]CAAGCTTTGACTCCT | 16798 |
rs29353008 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Lats1 | Mm_Celera | 10:7710426 | GGGGTGGCTTTGGTC[C/G]TGTAGCTTTCACTTC | 16798 |
rs29353858 | snp | C/G | 0.32 | 0.24 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7679885 | AAGGGTCTTTTCACT[C/G]CACCCTGGCTTGTGC | 16798 |
rs29355691 | snp | A/G | 0.5 | 0 | intron-variant | Lats1 | Mm_Celera | 10:7684945 | TCTTCTGCATAGGAA[A/G]CTCTAGGCCAGCCAG | 16798 |
rs29357019 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Lats1 | Mm_Celera | 10:7687503 | TGTAGATCAGGCTGG[A/G]TCAGAACTGGGAATG | 16798 |
rs29361645 | snp | C/T | 0.5 | 0 | intron-variant | Lats1 | Mm_Celera | 10:7690169 | GGGCTGCAGAGATGG[C/T]TCAGCAGTTACGAGC | 16798 |
rs29362611 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Lats1 | Mm_Celera | 10:7690032 | ATCCATGACAGCCAG[C/T]AAGGAGGACAGAAAG | 16798 |
rs29367816 | snp | A/C | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7688000 | GTAGGCAGAGGCAGG[A/C]GAATTTCTGAGTTCG | 16798 |
rs29368103 | snp | C/G | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7693706 | GGAGGCAGGAGCTCA[C/G]AGCAGGAACTGGAGG | 16798 |
rs29369540 | snp | A/G | 0.49827 | 0.0293608 | synonymous-codon | Lats1 | Mm_Celera | 10:7712941 | TTCACAGGGCTCAGA[A/G]CAACAGTCTGATGAA | 16798 |
rs29372925 | snp | C/T | 0.32 | 0.24 | upstream-variant-2KB, nc-transcript-variant, intron-variant | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7679854 | GGCCTGGCCTCCGCT[C/T]CTCTGCTTCTTTCCC | 16798 |
rs29378825 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Lats1 | Mm_Celera | 10:7703968 | GAGCTCACTCCTCAG[A/G]GGCTTTGCTCGCTCC | 16798 |
rs29382081 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lats1 | Mm_Celera | 10:7685683 | AGGCATGATCTTGCC[A/G]TGTAACTCAGGCTGG | 16798 |
rs29383817 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Lats1 | Mm_Celera | 10:7702334 | AAACGTTCCTCAGTC[A/G]ATGATGGTGCCCAAC | 16798 |
rs45633199 | snp | C/T | | | intron-variant | Lats1 | Mm_Celera | 10:7700398 | CTTCCTCTAACTAGG[C/T]CACAGGTCCTAATCC | 16798 |
rs45717348 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7715060 | TTTGTAAACAAGTAA[C/T]GATCTGCTCTTGGAA | 16798 |
rs45798245 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7715092 | GAGCCCGTGAAAGCA[A/G]CACAGCACAGACATG | 16798 |
rs45908937 | snp | A/G | | | intron-variant, upstream-variant-2KB | Lats1, BC020402, Pcmt1 | Mm_Celera | 10:7682576 | AGGTAATATGGTTGA[A/G]GTGATTCTCCAAGGC | 16798 |
rs45961372 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7687428 | GACTATAAGGTAGGG[C/T]TCTTGGTCATCATGT | 16798 |
rs45986932 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lats1 | Mm_Celera | 10:7691921 | GAGCTCATAAGGGCG[C/T]TTCTTTTGAGAGGAC | 16798 |
rs46055051 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Lats1 | Mm_Celera | 10:7687083 | ACGTAATCCCTACCA[A/G]CTATACTGTGCTGAT | 16798 |
rs46095836 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7692852 | GCAAAGCTCAGCAGT[A/G]TAAAAACAGTTCAGT | 16798 |
rs46293988 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7693305 | GGTCAGTCCTTGGCT[C/T]CCTGTGGACCCCAGG | 16798 |
rs46315011 | snp | A/G | 0.459184 | 0.136902 | intron-variant, utr-variant-3-prime | Lats1 | Mm_Celera | 10:7704574 | GGTTCTGTCACTGCC[A/G]ACAGTTGATCTCTGT | 16798 |
rs46604527 | snp | C/G | 0.35503 | 0.226867 | intron-variant | Lats1 | Mm_Celera | 10:7693447 | ACAGCAGTTCATAAG[C/G]TATGATGAGCTTTTC | 16798 |
rs46633192 | snp | A/C | | | intron-variant | Lats1 | Mm_Celera | 10:7699512 | GAAACTCTGTGTAAA[A/C]TAGCTTGGCCTTGAA | 16798 |
rs46774703 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7714588 | TATGTATATTATTTC[A/G]TTTTTTCAAGGTTTA | 16798 |
rs46862952 | snp | C/T | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7697452 | ACTTTTGTTCTTTCC[C/T]GTTGTTAATTATACT | 16798 |
rs46957484 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7715154 | TGTCTATAACACTGT[C/T]CTAACGGCACTGGTG | 16798 |
rs46988865 | snp | C/T | | | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7713393 | TAACCAAATATGAAA[C/T]ATAACCATATTTCCC | 16798 |
rs47062622 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lats1 | Mm_Celera | 10:7687433 | TAAGGTAGGGTTCTT[G/T]GTCATCATGTTAGCT | 16798 |
rs47361044 | snp | A/C/G | | | intron-variant | Lats1 | Mm_Celera | 10:7689423 | ATATCCACACAGTTG[A/C/G]GATTGAAACAAAAAC | 16798 |
rs47382550 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Lats1 | Mm_Celera | 10:7702322 | ATTCGCCAATGGAAA[C/T]GTTCCTCAGTCGATG | 16798 |
rs47496237 | snp | C/T | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7697684 | CTCCTCTCTTCAAAA[C/T]ACCTGCATCTGTCAA | 16798 |
rs47576339 | snp | C/T | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7693241 | AACACACCTTCAACA[C/T]TCACACCACCTGGGA | 16798 |
rs47850619 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7689712 | CTGAGTTTAAACACA[C/T]TTGGTTACCTACAAA | 16798 |
rs47851352 | snp | C/T | | | intron-variant | Lats1 | Mm_Celera | 10:7698269 | GACTGGGCGGCAATC[C/T]CCGTGGATAGATTGA | 16798 |
rs47888270 | snp | A/G | 0.132653 | 0.220748 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7714966 | AGGTTAAAGACCTAC[A/G]TCCTGTGAGTCAATT | 16798 |
rs47925066 | snp | A/G | | | intron-variant | Lats1 | Mm_Celera | 10:7696107 | GCTGGCCTTGAACTC[A/G]GAGATCTGCCTGCCT | 16798 |
rs47993860 | snp | G/T | 0.32 | 0.24 | synonymous-codon | Lats1 | Mm_Celera | 10:7701692 | GAGACACGGCCCATC[G/T]CTAGGAGAAAATGTG | 16798 |
rs48220726 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7700874 | ATGTCTCAGAACAGT[C/T]CTCCCTGTGTCTCCT | 16798 |
rs48231086 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7693521 | TCCCTAAGAATGAAG[A/G]ATAAGACATGGTCAG | 16798 |
rs48271626 | snp | C/T | 0.336735 | 0.234472 | intron-variant, downstream-variant-500B | Lats1 | Mm_Celera | 10:7705158 | GTGTTCACAGACACT[C/T]GTTTTCTTGTGCATT | 16798 |
rs48349214 | snp | A/G | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7687601 | GTGGCTTGTTGAAAT[A/G]TTTTGTCACTATGAA | 16798 |
rs48388358 | snp | A/G | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7687110 | TGATAAGCATGGGAA[A/G]TACAGAGCCCAATAA | 16798 |
rs48405432 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7692075 | CTGGAGTTTCTGTTG[C/G]TGAGGTCATGAAACC | 16798 |
rs48483244 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7698583 | CTCTGCTTTTACATG[A/G]GTGCAGTTACAACCA | 16798 |
rs48562222 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7713967 | TTAAAAGGGAACAAA[A/G]TTGCCATGAATTGAA | 16798 |
rs48728154 | snp | A/G | | | intron-variant | Lats1 | Mm_Celera | 10:7692771 | TTGTAAAATAAAAAA[A/G]TAACTTACATTTTAA | 16798 |
rs48840548 | snp | G/T | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7699641 | GGGTATTGATCCATC[G/T]AATGTTGCAGTTATA | 16798 |
rs48931342 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Lats1 | Mm_Celera | 10:7706178 | ATCCCTTAGGCGTGT[A/G]CATTTATAAAGTTAA | 16798 |
rs49435110 | snp | C/T | 0.124444 | 0.216185 | missense | Lats1 | Mm_Celera | 10:7702216 | CCACTGGTTCTGTGA[C/T]TCGGCAGCCACCACC | 16798 |
rs49456034 | snp | A/T | 0.35503 | 0.226867 | missense | Lats1 | Mm_Celera | 10:7697566 | CCGCTGTTGAATTCA[A/T]TAGTAAAATGAGTTA | 16798 |
rs49516046 | snp | C/T | | | intron-variant | Lats1 | Mm_Celera | 10:7703696 | TATTATTAGAAAGGG[C/T]TAAAATCACCAGGCA | 16798 |
rs49530397 | snp | A/G | | | intron-variant | Lats1 | Mm_Celera | 10:7688343 | CCTTCTTTTTCTCCT[A/G]TGATTTTTTTTCATT | 16798 |
rs49657500 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7693727 | GAACTGGAGGTAGGA[A/C]GTGGAGCAGAAGTTG | 16798 |
rs49886640 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7692222 | GTCTAGATTCATCGT[A/T]AGGAGAGAGTGACAG | 16798 |
rs49986867 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7714291 | CAGAACAGTGCTACA[A/G]TACAAATTGTTGGCA | 16798 |
rs50000601 | snp | A/G | 0.473373 | 0.11227 | intron-variant | Lats1 | Mm_Celera | 10:7692577 | ATCTATATAGCTCCA[A/G]TTTCAAGATTCCTTA | 16798 |
rs50014964 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7715177 | CACTGGTGTCTTGTG[A/T]TTCTGAGGGCTCCTG | 16798 |
rs50057428 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7691149 | TGCACCACCACTGTC[C/G]GGCTAGAAATATTGT | 16798 |
rs50061044 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7689849 | GGCACCGCAATATCA[A/G]GGTGGATCCTAAGGA | 16798 |
rs50067694 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Lats1 | Mm_Celera | 10:7688527 | CAGATAAACAGAGGA[C/G]TTAAAATACATTATG | 16798 |
rs50305468 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7694297 | TTCTACAAACATGAA[A/C]ATGGAGGCATAATTA | 16798 |
rs50326658 | snp | G/T | | | intron-variant | Lats1 | Mm_Celera | 10:7698217 | TTTTGTGACAGTGTC[G/T]CTTACTGAACTTTGA | 16798 |
rs50377032 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Lats1 | Mm_Celera | 10:7699978 | ACCCCAATTTAGGGC[C/T]CACATTTTTGTTTTA | 16798 |
rs50380981 | snp | A/G | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7690064 | GATCAGGAACAAAAG[A/G]TAGCCTTCATTTAGG | 16798 |
rs50712961 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lats1 | Mm_Celera | 10:7692508 | TGAGAGCATTGACTG[A/C]ACTTGTGGAGGACCC | 16798 |
rs50768365 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Lats1 | Mm_Celera | 10:7691787 | TCCACAGATGTTTCA[A/G]GATTTGCAGGCTGCT | 16798 |
rs50769262 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Lats1 | Mm_Celera | 10:7699462 | GTTAATCATGAATTA[C/T]GGAGACAGACACAGG | 16798 |
rs50838515 | snp | A/G | | | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7713316 | ATCTTTTGTATATAT[A/G]ATAAATAATTTTAAA | 16798 |
rs51151473 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lats1 | Mm_Celera | 10:7690859 | GGAGGAGGGAGTTGC[C/T]TAAGGTTCACTTAGT | 16798 |
rs51276522 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7715324 | AGCCCTCTGACCTTC[A/G]GGCTCTTCACTCAGA | 16798 |
rs51350840 | snp | C/T | 0.32 | 0.24 | intron-variant | Lats1 | Mm_Celera | 10:7687533 | GGTGCTTCAGCATCC[C/T]AGCTGTGGGTTACGG | 16798 |
rs51456481 | snp | C/T | 0.132653 | 0.220748 | intron-variant, utr-variant-3-prime | Lats1 | Mm_Celera | 10:7704385 | CTAAGTTTGGCATGC[C/T]ACCACTCTGAAAAGA | 16798 |
rs51542998 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lats1 | Mm_Celera | 10:7690793 | TTTAAAAGAGCTAAT[A/G]CCCTTCTAAGTAAGT | 16798 |
rs51585668 | snp | A/G | 0.32 | 0.24 | utr-variant-3-prime | Lats1 | Mm_Celera | 10:7716239 | GTATATAAGGGTTTT[A/G]TATTACAATGGAATC | 16798 |