SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6157213 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rab40c | Mm_Celera | 17:25899485 | TGCTGGGAAAGGTCA[C/T]TCTGCCCCTGTAACC | 224624 |
rs6157678 | snp | C/T | 0.5 | 0 | intron-variant | Rab40c | Mm_Celera | 17:25899525 | ACCTGCTTCACCTGC[C/T]CCCCCTCAGGNCTGT | 224624 |
rs6157696 | snp | C/T | 0.5 | 0 | intron-variant | Rab40c | Mm_Celera | 17:25899536 | CTGCNCCCCCTCAGG[C/T]CTGTAACAACTGGAC | 224624 |
rs6404739 | snp | A/T | 0.5 | 0 | intron-variant | Rab40c | Mm_Celera | 17:25899287 | aacacttcatcctcc[A/T]acctcaaTGGCAGGC | 224624 |
rs33446779 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rab40c | Mm_Celera | 17:25889594 | ATGCAGGCAAAACAC[C/T]CATCACATAAATACA | 224624 |
rs33479948 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rab40c | Mm_Celera | 17:25917373 | AATGCCCTGATGTTT[A/C]TAACTCCACAGAGAC | 224624 |
rs45682021 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25908030 | GGCTAACACAGATCT[G/T]AGACATACCTGAGTG | 224624 |
rs45690817 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25916335 | TGTGCCACCATGTCC[A/G]GTAAAAAGCTGTCTT | 224624 |
rs45785607 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25903648 | CTGAGTGCATGTCCC[A/G]CATGGTACACACTCT | 224624 |
rs45788743 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25888249 | CACCAACCCCAGTCA[A/G]GCCGTCTCTGAGCCG | 224624 |
rs45815565 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25904574 | GTCGTGGCCTGCAGA[C/T]TGGTAGGAGCAGTAA | 224624 |
rs45830729 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25905777 | ACAGAGATGCTACGC[A/C]AACGCCAACGCCAAC | 224624 |
rs45845194 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25911753 | AGAAGATGGTCAGCC[A/T]CTCAGGATATGGCGC | 224624 |
rs46023464 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25907873 | TTATGGGTAAGTGCA[C/T]CCTTCCAGCTGAGTT | 224624 |
rs46135919 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25885291 | CAGATCACTAGTATG[G/T]CCAAGAACTGAAGGG | 224624 |
rs46202300 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25895841 | TCCCCAACAGGACTG[A/G]TTGCTTTTAGTGTCT | 224624 |
rs46271209 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25884374 | TCTGTGACCACTCGG[C/T]GGCAAAGGTGCATGT | 224624 |
rs46370347 | snp | C/T | 0.32 | 0.24 | intron-variant | Rab40c | Mm_Celera | 17:25907066 | CTTGCCAGCCCATGA[C/T]TTTTTTTTTAGTATC | 224624 |
rs46497523 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25912133 | GAGGCCCTCAGCAAC[C/T]CTGGTAAGTGTCACT | 224624 |
rs46523688 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25889995 | TCCACACCATGGGTG[C/T]CACAGTGCATGCATG | 224624 |
rs46529618 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25916676 | AAATGGTGTTGACCA[C/G]TGGGTCACTAATCTG | 224624 |
rs46581031 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25896233 | GGTCTGAACATCACT[A/C]TCACGGGTCGGCGGT | 224624 |
rs46771746 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25892182 | GCAGAGACTGACCCT[A/G]AACAATGACTCTCTT | 224624 |
rs46897333 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rab40c | Mm_Celera | 17:25896940 | TCATTTTATTTTCCA[A/G]CCTTTTCCACAATTT | 224624 |
rs46981538 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25884006 | CTGGCTGCTGCATCT[C/T]ACCAGCTCAGGGCTC | 224624 |
rs46999851 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25897009 | AGATATACCACCCAC[A/C]GGGCAGGAAGCTGGT | 224624 |
rs47010143 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Rab40c | Mm_Celera | 17:25907540 | TCCCCCTCCACTTAA[C/G]CAGGTGTTAGGGACC | 224624 |
rs47156808 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25905889 | AACAGCAAAGCATAT[C/T]TCTTCTGTCTACTGA | 224624 |
rs47201093 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25902957 | CCCCGACAACACACT[G/T]ATTTCAGCTGATGGG | 224624 |
rs47293240 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25903071 | ATGGCAACTCAGCAT[C/T]GTGCTTCATAATCAA | 224624 |
rs47306600 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25905919 | AGAGCAAGCACACTC[A/G]GCATGGAAGCTCGGG | 224624 |
rs47334021 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rab40c | Mm_Celera | 17:25894525 | AAATATAAGACACAG[C/T]CATGAGCTAGCCAGT | 224624 |
rs47391817 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25917128 | GACCTATCATCCCAA[G/T]GCCACATATCAGAAC | 224624 |
rs47413702 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rab40c | Mm_Celera | 17:25900759 | ACTGTCCTGCAGGGT[A/G]TAATCACCTGACACA | 224624 |
rs47418108 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25890256 | ATGGCATGGAGAGGT[C/G]ATTTGCAGTGACTAT | 224624 |
rs47560015 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Rab40c | Mm_Celera | 17:25911610 | GGCCACTTTTATCAG[G/T]GCTACATGAACCTTT | 224624 |
rs47598262 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Rab40c | Mm_Celera | 17:25888075 | TGGTGCTGGATGCTT[C/T]GAGAATGATTCAAAA | 224624 |
rs47778306 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25904143 | TACATGTATTGGTAA[C/T]GAGAACAGACTGCCA | 224624 |
rs47810359 | snp | C/T | 0.32 | 0.24 | intron-variant | Rab40c | Mm_Celera | 17:25885365 | CTTCTGTGAGTCAAA[C/T]TGGCCCAGCCCACAT | 224624 |
rs47819014 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25890602 | CAGGAGAGGTACCTA[C/T]TGGACAACAACATAA | 224624 |
rs47864380 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25887678 | CAGGCGCCTTGAATT[C/T]CCTGTTTACGCCTGA | 224624 |
rs47867142 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25914848 | TGAGGGTTAAGAGAG[G/T]AAAACCAGGAAGTGC | 224624 |
rs47923623 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25895522 | GGAGCTGCATAACTA[C/T]CAGGGAACCTGCATT | 224624 |
rs47943381 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rab40c | GRCm38.p3 | 17:25883111 | GTCAGATATGGAAGC[C/T]GGAGCCAAGCCTGCT | 224624 |
rs48052378 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25903281 | TATTCAGTAGTCACT[C/T]TGCAGGTTAAGTCCA | 224624 |
rs48132950 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25891965 | ATGACAAGTGAACAC[C/T]TCACACTTCTACACA | 224624 |
rs48261516 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25911624 | GTGCTACATGAACCT[C/T]TGTAAAAGGCATACT | 224624 |
rs48285024 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25889823 | AAATTCTGAGGGGTG[C/T]ATCACAATGGAGATG | 224624 |
rs48462039 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25910775 | GAAGGTGCTGTCTCC[A/C]ATATAAGCAGTAAGT | 224624 |
rs48497020 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25896208 | TCTGGCAGAGCCACC[A/G]GCAAGCTCAGGTCTG | 224624 |
rs48499230 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25885407 | TTCATCCCCTGAGAA[A/C]ATGGCTGGGGCAGAA | 224624 |
rs48507018 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25904602 | TAACTAACCTCTCAT[G/T]GACAGGAGATGACTT | 224624 |
rs48522606 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25908282 | GCAAAGGCACATCGT[C/T]TCTGTGGGAAAGGCA | 224624 |
rs48648460 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25887957 | AGGGCTTGTACCACA[A/G]ATACAAACTAAGATG | 224624 |
rs48657213 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25907687 | GGCTATTTATTTTCC[A/G]CTTTTATTTAAAAAT | 224624 |
rs48949806 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25901120 | TGTAGTCATATGAAG[C/T]GAGCATACCAGTGCA | 224624 |
rs49064265 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25887773 | GAAGAGGCGCTCCTA[C/T]CGAGGCTGCCTGGGT | 224624 |
rs49100398 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25891441 | AATGTCCCCGAGGGA[A/G]CAGAATGATGGTGCT | 224624 |
rs49113720 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25903036 | CAGAAAGAAGAGCTA[C/T]AGCTGCATAACAATT | 224624 |
rs49140752 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25884315 | CATCATTAGGGGTTT[A/G]GTGTGGACAATGGCC | 224624 |
rs49143739 | snp | C/T | 0.32 | 0.24 | intron-variant | Rab40c | Mm_Celera | 17:25907642 | AGTACAGTACAAGTA[C/T]AAGTACACCATGTTG | 224624 |
rs49145628 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25888034 | AGAGCTTCCAGAAAT[A/G]ACAGGTAGAACAGAA | 224624 |
rs49161311 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25908761 | CAGTTTTGCTACTGA[A/G]CAGATTTATTTTTGC | 224624 |
rs49211841 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25911428 | AACTGGGAACCAAGA[A/G]CTCAAGGCCAAACAT | 224624 |
rs49212345 | snp | A/T | 0.260355 | 0.249785 | intron-variant | Rab40c | Mm_Celera | 17:25907076 | CATGATTTTTTTTTT[A/T]GTATCATTATTTCTT | 224624 |
rs49279862 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25902510 | TACTGGTGTCTTCAC[A/G]GGGCAAAAGGGACAC | 224624 |
rs49284222 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25900968 | CACGGCTTCACTTCA[A/T]TGTTCCACAGGAGCA | 224624 |
rs49311424 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rab40c | Mm_Celera | 17:25917555 | GCGATGTTCACACCC[A/G]AGGAACAAGCTAGAC | 224624 |
rs49321947 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25892038 | TAGAGAACTAACTTA[A/C]GCTTTCTCTGACTTC | 224624 |
rs49376127 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25915217 | GCCTGGCTTCAGATA[C/G]AGTAGAGAAAGGAAT | 224624 |
rs49400709 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25907713 | AAAATGAAAAGTCTT[A/G]GTTCCCTTTATTGTA | 224624 |
rs49422656 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25902590 | GCCCTAGATCTCCTG[A/G]ATGGGCTTCATTACA | 224624 |
rs49608258 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25914778 | AGATCTCCTAAGGTG[C/T]GGATAGCGAATCAAG | 224624 |
rs49666589 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25916929 | ATTAACAGGCCATGA[G/T]CATATAAACCACAAT | 224624 |
rs49674242 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25912079 | TAGTTCCCTTGGTCG[C/T]GCTTCACTCTTAGGC | 224624 |
rs49793542 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25916845 | CCCATCGTCAGCATC[A/T]CTCCACAGCTTCCTT | 224624 |
rs49856982 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25916717 | CCTGCCTGTAGCAGG[A/G]TCTTCACAGCATGCT | 224624 |
rs49882083 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25889686 | TCAATGCTTCATTGT[A/G]TCTGAAAGGAACTAT | 224624 |
rs49889722 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25893657 | CCCTGACTCCTCTAT[C/T]TCCATGACATACAGT | 224624 |
rs49973078 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Rab40c | Mm_Celera | 17:25907878 | GGTAAGTGCACCCTT[C/T]CAGCTGAGTTTAAGG | 224624 |
rs50130914 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25887617 | AGCATAAACAAATGG[C/T]GCACAGTACAGGAAG | 224624 |
rs50186276 | snp | C/T | 0.391111 | 0.206368 | intron-variant, upstream-variant-2KB | Rab40c, Gm10012 | Mm_Celera | 17:25902655 | TAGGGAGAAAAGGAA[C/T]GATCAAAACCTGAGA | 224624 |
rs50220261 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25912569 | CCTTTGAGTACTTCG[A/C]GTCTTGCCTCCTCTT | 224624 |
rs50242550 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Rab40c | Mm_Celera | 17:25887577 | GATTCCCTGAGTTAT[A/G]TATGCTAACACTGGG | 224624 |
rs50256704 | snp | A/G | 0.231111 | 0.249285 | utr-variant-3-prime | Rab40c | GRCm38.p3 | 17:25882951 | AAGCTCTGTAGCCCC[A/G]GCTGGAGATGTGTAT | 224624 |
rs50315781 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25894050 | GATCAGCAGGACCTG[C/T]AGCATAGCCTTCCTT | 224624 |
rs50328905 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25886086 | ACAGAGACAAAAGTA[C/T]CCTTACCCACAGGTA | 224624 |
rs50424922 | snp | A/C/T | 0.142012 | 0.225474 | intron-variant | Rab40c | GRCm38.p3 | 17:25908667 | CTTGGTTCCCCCACA[A/C/T]GGGTCTTTAGAATAT | 224624 |
rs50481921 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Rab40c | Mm_Celera | 17:25897758 | ACTTTGACATGCCAG[C/T]CTCTGGGCACCTGCT | 224624 |
rs50495604 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rab40c | Mm_Celera | 17:25894555 | TGAATCAGCCTCTCC[A/G]TTAGGTTTAAACATT | 224624 |
rs50580977 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25885161 | GGATTCCCTGTGAGT[G/T]TGAAGGAAGGAGATT | 224624 |
rs50582351 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rab40c | Mm_Celera | 17:25899913 | TATGTGTTCTAGCGT[A/T]TAGTGAGGTCCTGAG | 224624 |
rs50622796 | snp | C/T | 0.260355 | 0.249785 | utr-variant-3-prime | Rab40c | GRCm38.p3 | 17:25883386 | CTGGCTCACTTCCAG[C/T]CTGGAGTCCAGGACT | 224624 |
rs50628676 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25915469 | TAGTGCTGGAGATAA[A/T]GCAATGATTGAGACA | 224624 |
rs50774339 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25892205 | ACTCTCTTCTCTCAT[A/G]TCCCATTAACACCTT | 224624 |
rs50795228 | snp | A/C | 0.152778 | 0.230321 | upstream-variant-2KB, downstream-variant-500B | Wfikkn1, Rab40c | Mm_Celera | 17:25881989 | GGTCAGCTGCGGGGA[A/C]AGTTAACAAAGCCTG | 224624 |
rs50810016 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25905674 | ACTCAGCACGGGCAA[A/C]ACCTCAGAAACAGGG | 224624 |
rs50895463 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25905972 | AGAGCAAGCACACTC[A/G]GCATGGAAGCTCGGG | 224624 |
rs50971740 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rab40c | Mm_Celera | 17:25913718 | CCAACACCTGCTTTA[C/T]TGGCATGTAGCTAAT | 224624 |
rs51012410 | snp | A/T | 0.231111 | 0.249285 | utr-variant-3-prime | Rab40c | Mm_Celera | 17:25883321 | TCCCTGACAGCCCTT[A/T]AAAAATGTACAAAAC | 224624 |