SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13471742 | snp | A/G | | | missense, nc-transcript-variant, downstream-variant-500B | Kctd3 | Mm_Celera | 1:188974151 | CTGGACCAGTGTGAT[A/G]TGAGCACGTCCCGCT | 226823 |
rs13471743 | snp | G/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant, downstream-variant-500B | Kctd3 | Mm_Celera | 1:188974375 | CTCCCGGCCAAGGCG[G/T]TACCTGTTCACTGGC | 226823 |
rs30464858 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188987164 | CTATCTTCAATTATC[A/G]TTATTATTATTTTCT | 226823 |
rs30472739 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Kctd3 | Mm_Celera | 1:189007592 | CGACGCGGCGAAGCT[A/G]CCGCAATGCCCGCCC | 226823 |
rs30550178 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Kctd3 | Mm_Celera | 1:188983891 | GCCAAGAAACAACAC[A/T]AAGTGGCAGCAGCCG | 226823 |
rs30564431 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188975891 | CTAAACTAGACAATC[A/G]TTTTCAAAATTTAAA | 226823 |
rs30852165 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kctd3 | Mm_Celera | 1:188986470 | GACGTCAATTCTGCT[C/T]TGGAACATTCTTCAT | 226823 |
rs30981381 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188978287 | CAAGAGTGCACGCAC[A/G]CACAGCATTTTCATA | 226823 |
rs31055534 | snp | A/T | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188986002 | TTTCTCACAATACCG[A/T]CTATGCAGACTTCTG | 226823 |
rs31171554 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Kctd3 | Mm_Celera | 1:189003381 | GCCGGGCACCAGTCG[A/C]AGGGCAGCTTGGTGC | 226823 |
rs31233792 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Kctd3 | Mm_Celera | 1:188986372 | ATCACCTCTGTGTAC[A/G]TCATCATCTCTAGAC | 226823 |
rs31379647 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188987463 | TTACGGGAAGGGGCA[A/G]CGACAGCAGGAAAGT | 226823 |
rs31380383 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Kctd3 | Mm_Celera | 1:188984065 | GATCTACATGCAATC[A/G]GCTTCATGTGTGTTT | 226823 |
rs31422577 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188987968 | GCCTGCTCATGGACT[A/G]GATCTTGGGGAACCA | 226823 |
rs31469987 | snp | G/T | 0.401235 | 0.199068 | utr-variant-3-prime, nc-transcript-variant | Kctd3 | GRCm38.p3 | 1:188971636 | ACGTAGTGCACAGTG[G/T]AGCCTGGGACCAGGA | 226823 |
rs31474807 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Kctd3 | Mm_Celera | 1:188989848 | ACAGCCCTGCTGTAC[G/T]CTCTACGGGCGTGAG | 226823 |
rs31491924 | snp | A/G | 0.432133 | 0.171253 | intron-variant, upstream-variant-2KB | Kctd3 | Mm_Celera | 1:188999750 | CTGGCGGCAGGACTG[A/G]AATGAAATACAGGGA | 226823 |
rs31594161 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188972858 | ACTAACGTAATAACA[C/T]ACATACATTCATAAT | 226823 |
rs31659288 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd3 | Mm_Celera | 1:188990085 | GAGGCAGGAACCTGG[A/G]CACAGAGCTGATACA | 226823 |
rs31710058 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Kctd3 | Mm_Celera | 1:189007911 | CGAAGAAGGAGTGGG[C/T]GGGGCTGGTGAGAGG | 226823 |
rs31736935 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kctd3 | Mm_Celera | 1:188986528 | ACTTTGGAAAAGCTA[C/T]GGAAAGCTGGCTGCA | 226823 |
rs31739466 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Kctd3 | Mm_Celera | 1:188972830 | AAGTAGATCATATCA[C/T]ATACAATTACCAACT | 226823 |
rs31837284 | snp | C/T | 0.290657 | 0.246672 | utr-variant-3-prime, nc-transcript-variant | Kctd3 | GRCm38.p3 | 1:188971516 | TCAAACAGACATTGT[C/T]CCCACTGGAACGACT | 226823 |
rs31881642 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Kctd3 | Mm_Celera | 1:188976828 | CAGACCTATGCCAGC[A/G]TCACACACAAGCTCA | 226823 |
rs31915886 | snp | G/T | 0.265928 | 0.249492 | utr-variant-3-prime, nc-transcript-variant, downstream-variant-500B | Kctd3 | GRCm38.p3 | 1:188971847 | CTCTAAGGGAACACA[G/T]TAACACCAGCAGGGA | 226823 |
rs32063497 | snp | A/T | 0.21875 | 0.248039 | intron-variant | Kctd3 | Mm_Celera | 1:189002566 | TCATCTCCTGATGAA[A/T]GGTAACTCCTTAAAC | 226823 |
rs32112227 | snp | G/T | 0.265928 | 0.249492 | intron-variant | Kctd3 | Mm_Celera | 1:188989644 | CACTCCAGCTTAGGC[G/T]CAAGGATCCTGATGG | 226823 |
rs32230733 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kctd3 | Mm_Celera | 1:188986222 | CTCAGCTGACTTGTT[C/T]CCTATTTTCTAGTCC | 226823 |
rs32307398 | snp | A/G | 0.432133 | 0.171253 | downstream-variant-500B | Kctd3 | Mm_Celera | 1:188970624 | TGAGAAGAGATAGAT[A/G]CTTCTCCACTCAGTG | 226823 |
rs32379036 | snp | A/G | 0.5 | 0 | intron-variant | Kctd3 | Mm_Celera | 1:188993215 | GCCAGGCCAGCAATT[A/G]GAAAGGTAAATTAGA | 226823 |
rs32389274 | snp | A/C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Kctd3 | GRCm38.p3 | 1:189007896 | GGCGCTTCACGCTTA[A/C/T]GAAGAAGGAGTGGGC | 226823 |
rs32399853 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188978298 | GCACGCACAGCATTT[G/T]CATATGTGTGTGTAC | 226823 |
rs32439475 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd3 | Mm_Celera | 1:188989855 | TGCTGTACGCTCTAC[A/G]GGCGTGAGCAAATTC | 226823 |
rs32459979 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188987712 | ACCATCCCCAGTTAC[C/T]ACAGCCTACTGCCTG | 226823 |
rs32478005 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Kctd3 | Mm_Celera | 1:188976352 | AGGCAATCTGGAATG[C/T]CCCACCTGAGAGACA | 226823 |
rs32496947 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188987464 | TACGGGAAGGGGCAA[C/T]GACAGCAGGAAAGTG | 226823 |
rs32537483 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188984211 | TGACCCAGGGGTCAG[A/G]TGGGGTTGTCATCTC | 226823 |
rs32595812 | snp | C/T | 0.5 | 0 | utr-variant-3-prime, nc-transcript-variant | Kctd3 | Mm_Celera | 1:188971460 | GCAGCTGGAGGGACT[C/T]GCTTGTGAGCACCCC | 226823 |
rs32606571 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188990033 | GAGGGAAGGCTCTAC[G/T]TCACCTTCCAGCTTG | 226823 |
rs32637232 | snp | A/G | 0.265928 | 0.249492 | intron-variant | Kctd3 | Mm_Celera | 1:188983843 | CATGTAAAGCCAAAG[A/G]ACTTAGGTCACCACA | 226823 |
rs32682402 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Kctd3 | Mm_Celera | 1:188986489 | AACATTCTTCATCCA[A/G]CTGGCTGAATCTATG | 226823 |
rs32727096 | snp | C/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Kctd3 | Mm_Celera | 1:188999703 | CAATCGCCTGTTTTC[C/T]GCAGAGCAGCAGTCG | 226823 |
rs32731861 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd3 | Mm_Celera | 1:188978264 | GACCTCCAACGTGTG[C/T]GCTCAGGCAAGAGTG | 226823 |
rs32764697 | snp | C/T | 0.5 | 0 | intron-variant | Kctd3 | Mm_Celera | 1:188985972 | GGAGCCTCTCCACTG[C/T]CCACCACTGCGCTGT | 226823 |
rs36243035 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Kctd3 | Mm_Celera | 1:188970857 | GCAGTCCGTGCTTTT[A/G]GGAAGCCACTCTTCC | 226823 |
rs36257456 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188980009 | TAATGAAATCCTCAG[A/T]TCTCAGGCCAGTAGT | 226823 |
rs36271909 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Kctd3 | Mm_Celera | 1:188998298 | TCACAGTAAGTAGTA[A/G]AGCTGGGTGATACAT | 226823 |
rs36275544 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188987787 | CCTAAGCCTCCATTA[G/T]GGAAGCCGAGAGCAG | 226823 |
rs36308516 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Kctd3 | Mm_Celera | 1:188982423 | CCTACATGAGGAAGG[A/G]ATTTTTCCTTTGGGT | 226823 |
rs36308569 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188990745 | GACAGCTGTGTCTTC[A/G]TGCTCTGGGCACTCC | 226823 |
rs36331144 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:189003273 | GTAGGAGTGAGATCC[A/T]GAGACTAAGGAGCCA | 226823 |
rs36339593 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188989371 | GTAAGCTATATGACA[C/T]GTATTTACCCGGCCT | 226823 |
rs36359061 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | GRCm38.p3 | 1:188988269 | ACAACAGAAGGGAGA[C/G/T]CAGTCAAGACAGTGA | 226823 |
rs36379580 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188976837 | GCCAGCGTCACACAC[A/G]AGCTCAAGGCCGAAG | 226823 |
rs36388604 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188990692 | GCTGAAACTTTTAGG[C/T]AATGCACAAAAGGAA | 226823 |
rs36391207 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon, nc-transcript-variant | Kctd3 | GRCm38.p3 | 1:188978591 | GGAGCCTGGCTGCGT[A/G]GAGATCATCCCTCTG | 226823 |
rs36411174 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:189000832 | AATTCGATGCAGACA[C/T]ATCTGTTTTGCTGCC | 226823 |
rs36420113 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188989242 | GAAACTCAGAAGAAA[A/G]CATCAGTAGTCCTGC | 226823 |
rs36441479 | snp | A/C | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Kctd3 | Mm_Celera | 1:188999105 | CTAACTTCAACAACG[A/C]TGCTTGCATACTCAG | 226823 |
rs36446483 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:189005183 | CTTGCTACAAAATCT[G/T]AACTATGAAGCTAAA | 226823 |
rs36449077 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:189000782 | AAAGATGCTTACAAC[A/G]GACATGAACTGGCTT | 226823 |
rs36461576 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon, nc-transcript-variant | Kctd3 | Mm_Celera | 1:188983038 | GAGGTAAACGCTCAG[C/T]GCGGTGACGGCGTCA | 226823 |
rs36461960 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188991152 | ATGTGTGACCACACC[A/G]ATTCCAAGGTCAGGA | 226823 |
rs36504819 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Kctd3 | Mm_Celera | 1:189004099 | GAGACTTTGTCTCAA[C/T]ATACATCTATACACA | 226823 |
rs36506699 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188993346 | AAGTCTGTAATTACC[C/T]TTTTCGGCCACCAGG | 226823 |
rs36513280 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Kctd3 | Mm_Celera | 1:188994275 | CAGCAACTCATACAA[A/G]TTCTCCATTAATTCA | 226823 |
rs36515743 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188985868 | ATGTGTGGACAGCAA[A/G]GCACAGAGCAGAACT | 226823 |
rs36515966 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188986653 | CCAGTTCCTTTTAAA[C/T]TGTCAATCTGTTCAA | 226823 |
rs36590104 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188999991 | TACTGCACTGTAGCC[A/T]ACCATTAGCTATACA | 226823 |
rs36593439 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kctd3 | Mm_Celera | 1:188980284 | GAACACAGAACACTG[C/T]TGACGGGTGCTTTAA | 226823 |
rs36621394 | snp | C/T | 0.244898 | 0.249948 | downstream-variant-500B | Kctd3 | Mm_Celera | 1:188970638 | TGCTTCTCCACTCAG[C/T]GCACCAGGACACTGA | 226823 |
rs36653807 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188980121 | AGAAGACAAAGAACT[A/G]AAGCCATCATGAATG | 226823 |
rs36655629 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188991592 | TGAGAAGAGAGAAAG[A/T]CCTGCATGCCTGTGT | 226823 |
rs36656504 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188975484 | ATATTAATGAGGTAC[A/G]CTTATGAGACATGTC | 226823 |
rs36668031 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:189000803 | GAACTGGCTTTTTGA[G/T]TTAATGTTTAACTAA | 226823 |
rs36695384 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188996596 | TTCCTCATACTTTCA[A/G]ACAGGATCTTTTCAA | 226823 |
rs36695919 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188996848 | GCAGCTTCACTCTCA[C/T]GCAAGGGCACGGTCT | 226823 |
rs36724977 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188978725 | TACATCAAGCAGATC[A/G]TTGTACATTTGGAAA | 226823 |
rs36732137 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188994237 | GAGATAAATAAGCTA[A/G]AATGGAGACAGATGC | 226823 |
rs36746452 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188988385 | GGAGAATCCGAGGAC[C/G]GTAAGAAAGGAGAGT | 226823 |
rs36747933 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kctd3 | Mm_Celera | 1:188995389 | ACACATCCTACCTTA[C/G]TAGTTATGCCCAACA | 226823 |
rs36765850 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Kctd3 | Mm_Celera | 1:188999441 | CATCTATACACTCCA[G/T]GTCCATCACAGGCTG | 226823 |
rs36770998 | snp | A/G | 0.35503 | 0.226867 | intron-variant, upstream-variant-2KB | Kctd3 | Mm_Celera | 1:188999557 | AAACTGACAGGCAGC[A/G]AGTTCAAACAGTGCC | 226823 |
rs36787473 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188986587 | AAACAGGCCACTGGG[C/T]GAGAACTGCTCCAGT | 226823 |
rs36789398 | snp | A/G | 0.231111 | 0.249285 | downstream-variant-500B | Kctd3 | Mm_Celera | 1:188971019 | GACATGGTAAGTACA[A/G]TGTTTCTTTTTTACA | 226823 |
rs36789565 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188988351 | GGGTTTTCCAAAGGT[C/T]CACAGGCACTGTCAC | 226823 |
rs36797745 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Kctd3 | GRCm38.p3 | 1:188996572 | ACATATTATCTGTTA[C/T]GCTTGAATTTCCTCA | 226823 |
rs36806250 | snp | A/G | 0.260355 | 0.249785 | synonymous-codon, nc-transcript-variant | Kctd3 | Mm_Celera | 1:188972458 | CCTCTCAGACATAGC[A/G]CACTCCCCTGCTGCC | 226823 |
rs36853951 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Kctd3 | Mm_Celera | 1:188979955 | AAAAAAACTTGGAAA[A/T]TACCAAGAAATAGTT | 226823 |
rs36866138 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:189002517 | GAGGTCAAATCCACA[C/T]CTAAGCACTAAGACA | 226823 |
rs36874701 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188983129 | AACTTCTGCATGTCT[A/G]CGGACAAGGACACAT | 226823 |
rs36879682 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188984560 | ACCCATGCTCTGGCC[C/T]AGGCTGGGCAGGTCC | 226823 |
rs36887202 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188978661 | GCACACACTAGGAAA[A/G]AAAGAACACAATACA | 226823 |
rs36913521 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188991103 | TATTCTGAAGATGTC[C/G]GCTGACAGAGGCGTG | 226823 |
rs36930035 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188984010 | TTAGCACTGCTTCAA[A/G]GAGCTAGCACTTCTC | 226823 |
rs36939190 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Kctd3 | Mm_Celera | 1:188970930 | CCTCCATCTACCAGG[C/T]TGAGATTAAGGTTCA | 226823 |
rs36951107 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188980103 | CTAAGCTTAGCAGGA[C/T]GGAGAAGACAAAGAA | 226823 |
rs36968953 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188985072 | CTGCCACGTTACTCA[A/G]GCTGAGCTACCTTAC | 226823 |
rs36970148 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188980391 | GAACTCAGCTTCTAG[A/G]AGGAGGCAGACAGCA | 226823 |
rs36970595 | snp | C/G/T | 0.231111 | 0.249285 | intron-variant | Kctd3 | Mm_Celera | 1:188985295 | GTTTATAAGGTTAAA[C/G/T]GCAGATGCTATGCTT | 226823 |