SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6240499 | snp | C/T | 0.35503 | 0.226867 | intron-variant, missense | Lats2 | GRCm38.p3 | 14:57722442 | TTGAATTCGCACACA[C/T]TGCAAAGCTGTAGCA | 50523 |
rs6241041 | snp | C/T | 0.5 | 0 | intron-variant, missense | Lats2 | GRCm38.p3 | 14:57722539 | gaaacagacacgcac[C/T]aggaatatgcatctg | 50523 |
rs6242177 | snp | A/G | 0.5 | 0 | intron-variant | Lats2 | Mm_Celera | 14:57722806 | ttcaccccagcactt[A/G]agaggctgaggcaan | 50523 |
rs6254934 | snp | A/G | 0.5 | 0 | intron-variant | Lats2 | Mm_Celera | 14:57722821 | nagaggctgaggcaa[A/G]catatctctgtgagt | 50523 |
rs6255482 | snp | C/T | 0.5 | 0 | intron-variant | Lats2 | Mm_Celera | 14:57722924 | gcacagactgtcctt[C/T]cagggacctggactc | 50523 |
rs6348543 | snp | C/G | 0.5 | 0 | intron-variant | Lats2 | Mm_Celera | 14:57701806 | gaaagctcccaactg[C/G]ctgggactccagcct | 50523 |
rs6362111 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Lats2 | Mm_Celera | 14:57702064 | TCCTACAGACTCCTC[C/T]GCTCTGCTAGATCTG | 50523 |
rs6362585 | snp | C/G | 0.5 | 0 | intron-variant | Lats2 | Mm_Celera | 14:57702121 | GGGTCTTATCCACTC[C/G]TAGGGATAAGCCCCG | 50523 |
rs13467452 | snp | C/T | | | utr-variant-3-prime | Lats2 | Mm_Celera | 14:57690964 | CTAGAAAAGGAAGAG[C/T]TGGAGAGCGTGAGGC | 50523 |
rs30168184 | snp | A/G | 0.387812 | 0.208586 | downstream-variant-500B | Lats2 | GRCm38.p3 | 14:57689424 | GGTGGAGTTGCAGCC[A/G]TTCACCCTTGAGTTT | 50523 |
rs30203842 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lats2 | Mm_Celera | 14:57692465 | ATTTATTATATGTAA[A/G]TACACTGTAGCTGTC | 50523 |
rs30207480 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Lats2 | GRCm38.p3 | 14:57704716 | GCATGGTGGGGTAAT[C/T]CCAGCACTTGGGAGG | 50523 |
rs30296166 | snp | A/G | 0.444444 | 0.157135 | utr-variant-5-prime, upstream-variant-2KB, missense | Lats2, Gm29850 | Mm_Celera | 14:57745973 | CCGGGCGCCGGTGGC[A/G]GCAGTGGTTGCTGAC | 50523 |
rs30308284 | snp | A/T | 0.375 | 0.216506 | utr-variant-3-prime | Lats2 | GRCm38.p3 | 14:57691112 | TCCATACTGTACTAA[A/T]TTTTTAAAAATACTG | 50523 |
rs30449921 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Lats2 | GRCm38.p3 | 14:57694853 | AGCAGATGGCTTCAC[A/G]GGAAAGTTTACAAAT | 50523 |
rs30630749 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Lats2 | GRCm38.p3 | 14:57692899 | CCAGCTTGAAAAAGC[C/T]GCCATTCAGTCTCAA | 50523 |
rs30717602 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Lats2 | GRCm38.p3 | 14:57713151 | TGTGGTTTGTCTCTG[G/T]AATAGCAAGCCAAAG | 50523 |
rs30718578 | snp | C/G | 0.465374 | 0.126941 | utr-variant-3-prime | Lats2 | GRCm38.p3 | 14:57689770 | AAGAACCTACCACAT[C/G]AAACTATGTCAGAGC | 50523 |
rs30722253 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Lats2 | Mm_Celera | 14:57709103 | TACAAGAGCCTCAGG[C/T]TTTACCTGATGGAAA | 50523 |
rs30733440 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lats2 | Mm_Celera | 14:57692513 | AGGGCGTCAGATCTC[A/G]TTAGGGATGGTTGTG | 50523 |
rs30785620 | snp | A/C/T | 0.391111 | 0.206368 | intron-variant | Lats2 | GRCm38.p3 | 14:57719065 | CTCCTTTGTACTGTT[A/C/T]ATTTCCTTAAAAGCA | 50523 |
rs30821533 | snp | G/T | 0.415225 | 0.187619 | intron-variant | Lats2 | GRCm38.p3 | 14:57725316 | GGCAGCACAGTTTTG[G/T]CAGGAATGGCCTTCT | 50523 |
rs30942551 | snp | C/T | 0.265928 | 0.249492 | intron-variant | Lats2 | GRCm38.p3 | 14:57718173 | TGACTTCAGAGGACA[C/T]AACTCCTGAGGTGGA | 50523 |
rs30960969 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Lats2 | GRCm38.p3 | 14:57718650 | CTGAAACTGTAAGCC[A/T]GCCCCAATTCAATGT | 50523 |
rs31023845 | snp | A/T | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Lats2, Gm29850 | GRCm38.p3 | 14:57747636 | TGAGGAGGCAGAGGC[A/T]GGCTGACCTCAGAGT | 50523 |
rs31135349 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B | Lats2 | GRCm38.p3 | 14:57689403 | CATGGTTGTCATGAC[A/G]ACACAGGTGGAGTTG | 50523 |
rs31263615 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Lats2 | GRCm38.p3 | 14:57727009 | TAAATTGACAGAGTG[A/G]GATTCTAAAGTCAGC | 50523 |
rs31386498 | snp | A/G | 0.455 | 0.143091 | intron-variant | Lats2 | GRCm38.p3 | 14:57691999 | CTTGAACCCATCTGG[A/G]TGGTCATTAAAAATA | 50523 |
rs31410669 | snp | A/G | 0.33241 | 0.236027 | utr-variant-3-prime | Lats2 | GRCm38.p3 | 14:57689819 | TTACTACAAAATAGC[A/G]AGAATACTGTAAGTC | 50523 |
rs31496020 | snp | C/G | 0.375 | 0.216506 | intron-variant | Lats2 | Mm_Celera | 14:57692517 | CGTCAGATCTCGTTA[C/G]GGATGGTTGTGAGCC | 50523 |
rs31514553 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Lats2 | GRCm38.p3 | 14:57692636 | GAATTTTTAAAAGCA[C/T]ACAAACAGCACATGA | 50523 |
rs45674677 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57713192 | GTGAACAGCCTTGAT[A/G]AGAAGTGGGCATGAG | 50523 |
rs45831864 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57705127 | TCACCACCTGGGATT[C/G]CCGGGTAGGAAAGCA | 50523 |
rs45881225 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Lats2 | Mm_Celera | 14:57727130 | ATGGGAGCCTCTAAT[A/T]ACTTCCACCTACTTA | 50523 |
rs45917620 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57713824 | CACCAGCTGGGTCCT[A/T]CAGTGACAGTAAAAA | 50523 |
rs45944432 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57706517 | AAAGCTTCTCCTATC[C/T]GCATGAAGACTGCCT | 50523 |
rs46016376 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57713041 | GTGCAAGTGTCACCA[C/T]AGCTCATCAGCTGCG | 50523 |
rs46071571 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lats2 | Mm_Celera | 14:57726566 | AAAGTCTCTGGCAGG[C/T]GGTGCAAACCCAAGA | 50523 |
rs46114470 | snp | A/C | 0.231111 | 0.249285 | synonymous-codon | Lats2 | GRCm38.p3 | 14:57697304 | ATCCTTCTTCCTGAG[A/C]GTCTTCATGGCGTAC | 50523 |
rs46115083 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57697502 | ACAGAGCCCAGCCTG[C/T]ACACAAGGAAAATCA | 50523 |
rs46171015 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57703528 | GAAGCTACGAAGACA[C/G]GTTACCTTAGAGAAG | 50523 |
rs46202602 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Lats2 | GRCm38.p3 | 14:57699408 | CTCTTCATCTCTGCT[A/G]TTCTTGCGGACAGGC | 50523 |
rs46230115 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Lats2 | Mm_Celera | 14:57725595 | GCATCTATGGCCAGC[A/G]AGTGCAGGTAGTGCT | 50523 |
rs46247524 | snp | C/T | 0.132653 | 0.220748 | intron-variant, missense | Lats2 | Mm_Celera | 14:57722395 | GAAGACGGCTGGCTC[C/T]GTGCTTCAGGTACAA | 50523 |
rs46310226 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Lats2 | Mm_Celera | 14:57689341 | TCAAGGTTACTCCTC[A/G]CTGTGCCAATAGCTT | 50523 |
rs46324828 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Lats2 | Mm_Celera | 14:57690896 | AGATAAGCGGTCCTC[A/G]TGACTTGAGCAGAGC | 50523 |
rs46329769 | snp | A/C | 0.18 | 0.24 | intron-variant | Lats2 | Mm_Celera | 14:57726230 | ACTGGGCTAGAGCAG[A/C]GCTGAGCTGAGGGAC | 50523 |
rs46348909 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57695928 | TGAGATAAAAAGCCC[A/G]AGGTTCCCGGGTACA | 50523 |
rs46465977 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57709008 | CCAGATTAACAGTGA[A/C]CTGGATGAGCTCCTT | 50523 |
rs46504024 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, downstream-variant-500B | Lats2 | Mm_Celera | 14:57691426 | CCTGCGGAAGGTGAA[C/T]TCATAGAAGGCGTGC | 50523 |
rs46555094 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57712051 | GTGCGACACCAAAGT[A/G]GGCTTACCACTGTAT | 50523 |
rs46604085 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57693766 | TAGGACTGTGCTTCT[A/G]TAAATCCACTAACCA | 50523 |
rs46617459 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Lats2 | Mm_Celera | 14:57717075 | AGGCTGAGGTACACA[C/T]GCCGTGGTGCTCCAT | 50523 |
rs46759392 | snp | C/G | 0.32 | 0.24 | intron-variant | Lats2 | Mm_Celera | 14:57737784 | TATGAAGAAAGCAGC[C/G]ATACAAAGTTCTGTT | 50523 |
rs46773745 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Lats2 | Mm_Celera | 14:57696757 | ATACAGTAAGAAAGT[A/C]CACTAACAAAGCAAC | 50523 |
rs46775462 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57692081 | TGTTCAGGCTTAGGC[C/T]CAGTGTGGAACTAGA | 50523 |
rs46810390 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57713746 | CACATGCACGCACAC[A/G]TGAGATGTTCTGTTA | 50523 |
rs46837087 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Lats2 | Mm_Celera | 14:57712619 | AGAGAACACCTGCCC[C/T]AGCAAGTACAGGGCC | 50523 |
rs46913810 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Lats2 | Mm_Celera | 14:57697376 | AAAGGCACCGATGCC[C/T]AGAGTCTTGATTTTC | 50523 |
rs47037022 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57710322 | CACCTGAGAAGACAC[A/C]GAAGTCTCACCCACT | 50523 |
rs47039847 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57740894 | AGAAACAGGAAGTGA[C/T]GGCCTGATGCCCTGA | 50523 |
rs47076745 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Lats2 | Mm_Celera | 14:57690868 | GGGAAAATACAAAAC[A/T]AAGCCACTGTGTAGA | 50523 |
rs47117487 | snp | A/C | | | upstream-variant-2KB, intron-variant | Lats2, Gm29850 | GRCm38.p3 | 14:57746950 | CTCACCACCACCACC[A/C]CCACCCCCACCCCCA | 50523 |
rs47146484 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lats2 | Mm_Celera | 14:57716801 | TGTCATGCCAGGCCA[C/T]TTATATGAAACAAAG | 50523 |
rs47177413 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Lats2 | Mm_Celera | 14:57712087 | TGCCATGGTCTGTCC[A/G]CACCCTGAACTACAG | 50523 |
rs47192235 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57693276 | CTAGTAAGCAGAAAA[C/T]GCAAAAACTAATTGT | 50523 |
rs47303382 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57712227 | CATTGGGTGGCAGCA[C/T]CCCTCAGAATGACTC | 50523 |
rs47346007 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon | Lats2 | GRCm38.p3 | 14:57697007 | ATCCAGGTCGATGAG[G/T]ATGTTGTCAGGCTTG | 50523 |
rs47418142 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lats2 | Mm_Celera | 14:57741220 | GGACTTCCACAGAGC[G/T]TCCCGGTGTGTTCTC | 50523 |
rs47456455 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, intron-variant | Lats2 | Mm_Celera | 14:57694359 | CAAGAAAGGCGGCTG[C/T]CCAACCAGCATCTCA | 50523 |
rs47609612 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Lats2 | Mm_Celera | 14:57714425 | CTCTTAGCTACTTTT[G/T]GAAGCATCCGCTCCT | 50523 |
rs47620380 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57691905 | TGTTGGGCCACCACA[G/T]CGCACAATTCGGTAT | 50523 |
rs47719511 | snp | G/T | 0.231111 | 0.249285 | utr-variant-3-prime | Lats2 | Mm_Celera | 14:57690027 | GATGTGTTCCATCCT[G/T]GAAAAGCAAAAGAAA | 50523 |
rs47739834 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57692675 | ACACATGCTCAGTGG[C/T]GCCCTACAGCACACC | 50523 |
rs47768097 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57694078 | GAGAGAGAGCCACAA[A/G]TGGTTTACATAAAAT | 50523 |
rs47846084 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Lats2 | Mm_Celera | 14:57689981 | GCTAAGAACCTTGGT[A/G]AGAAGATTTGGCATA | 50523 |
rs48070253 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57692419 | CGAGAACTCCAACAA[A/G]TGATCTGAATTTTTT | 50523 |
rs48129669 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, utr-variant-3-prime | Lats2 | Mm_Celera | 14:57691714 | GATGAGGTCTCGGGC[C/T]TCAGCGCTGAGCCTC | 50523 |
rs48214119 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57694595 | ACAGGCAACAGACAC[G/T]TGGGCTTTCTTATTT | 50523 |
rs48233644 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lats2 | Mm_Celera | 14:57714885 | AGCTCCAAGACTCCT[A/G]TTTTTAATGTGGCCA | 50523 |
rs48243041 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57707559 | GTCCTCCTCAGGCTG[A/G]CTGCTGCCTTTCTCG | 50523 |
rs48248722 | snp | A/C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Lats2 | Mm_Celera | 14:57690757 | GACACCGGAGTCACA[A/C/T]CCACCAGCTCTCTGC | 50523 |
rs48260786 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57703802 | AATTGAAAAGATGGT[G/T]CCCGTCTACCCAGGG | 50523 |
rs48322684 | snp | G/T | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57715195 | TTTATTATTGTTAGC[G/T]AAGCGTCCAACTCTT | 50523 |
rs48421038 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lats2 | Mm_Celera | 14:57719834 | GGTTATAGTAAGTGA[C/T]GAAACTATTCACTAG | 50523 |
rs48495829 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57715338 | ATGGTGGACTGAGAG[A/G]CCTGTAGGATGAGCA | 50523 |
rs48523157 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Lats2 | Mm_Celera | 14:57724714 | AAAGCTTCCTGGAGC[C/G]GCCTCGAAGACACTA | 50523 |
rs48692462 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Lats2 | Mm_Celera | 14:57718108 | GCCCTGCAAGACATT[C/T]CATAGTTCAGATACA | 50523 |
rs48696328 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57698360 | AACAGAAAACAAGCA[A/G]TGACTCCGGGCCAAC | 50523 |
rs48796964 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57741542 | AGAGTGGAGCTCAGC[A/C]GGGGCCTGGAAGGGT | 50523 |
rs48827358 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57691797 | AGAACCACTGTTAGC[A/G]CCCCATCGATCTAAG | 50523 |
rs49013843 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57713948 | CTCTGCTCAGCTCAC[C/G]TCTGCACGGTCAGCT | 50523 |
rs49016249 | snp | A/G | 0.297521 | 0.245442 | intron-variant | Lats2 | Mm_Celera | 14:57706818 | CAAGACCTCACGGCT[A/G]GCTTGTGCCTGAGAG | 50523 |
rs49048346 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57705423 | CTTCCATTCAGGCCC[A/T]GCCAGCAGCCAGGGA | 50523 |
rs49069590 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Lats2 | Mm_Celera | 14:57740053 | GCCCAACAGCCAGGG[C/T]AGAGTAGACTCTGAG | 50523 |
rs49092203 | snp | A/T | 0.152778 | 0.230321 | intron-variant | Lats2 | Mm_Celera | 14:57707443 | AAAGGATTTCATTTC[A/T]TGGAGAGAACAAAGA | 50523 |
rs49214752 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Lats2 | Mm_Celera | 14:57692072 | TGTCTGCGTTGTTCA[G/T]GCTTAGGCCCAGTGT | 50523 |
rs49250362 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Lats2 | Mm_Celera | 14:57725155 | CCTGTGCAGGAAGGC[A/T]TTCTTTCCTACTCCT | 50523 |
rs49344750 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Lats2 | Mm_Celera | 14:57705752 | CCAAATACTTACTGG[C/T]GTTTGCTTTGGTGGA | 50523 |
rs49369889 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Lats2 | Mm_Celera | 14:57697868 | TGGTGAGCTGACAGT[A/G]AGCCCAGCTTTTAGG | 50523 |