SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3662341 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Kdm5b | GRCm38.p3 | 1:134598026 | TTTAAGGGCTGTTTA[A/T]GTCAGTTTAGAAGTA | 75605 |
rs3662947 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Kdm5b | GRCm38.p3 | 1:134598128 | GAGATGCATTTGTCT[C/T]TGTGGCTTTGTTTTC | 75605 |
rs3662974 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Kdm5b | Mm_Celera | 1:134598144 | TGTGGCTTTGTTTTC[A/G]CATTTGCTCTTCTGT | 75605 |
rs3663508 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Kdm5b | Mm_Celera | 1:134598211 | CCGAGTTTGCTACTG[C/T]TGTGATTACAGGCAG | 75605 |
rs3672057 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Kdm5b | GRCm38.p3 | 1:134594490 | ATTAATTTAAAACCT[A/G]ATACTTATTTTTTTG | 75605 |
rs3672698 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm5b | GRCm38.p3 | 1:134594605 | CTTCCAGTTGCTAGG[A/G]ATACAGGTGTGTCCC | 75605 |
rs3682613 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | GRCm38.p3 | 1:134572373 | CTGGCTGTCCTGGAA[C/T]TCACTCTGTAGACCA | 75605 |
rs3696869 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134596218 | TCCCTGTTTTCCTCC[C/T]TCCATTCTCTCTTCC | 75605 |
rs3698612 | snp | C/G | 0.495868 | 0.0452663 | intron-variant | Kdm5b | GRCm38.p3 | 1:134572708 | CATGGCAATAGTAAG[C/G]TACAGATACAGAACG | 75605 |
rs3706166 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kdm5b | Mm_Celera | 1:134568484 | CCCCTCAACCATTAT[C/T]TGGGAAGCCCAATAA | 75605 |
rs3707184 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kdm5b | GRCm38.p3 | 1:134610255 | TTGCAGGAATCTTTC[C/T]TAAAATGAATCCCTT | 75605 |
rs3709077 | snp | A/G | 0.290657 | 0.246672 | utr-variant-3-prime | Kdm5b | Mm_Celera | 1:134632011 | TGTCTAGTTTCTGGT[A/G]TCACTGCACTAGTGA | 75605 |
rs3713050 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134596601 | CTGGTGAGTTGGTGG[C/T]ATCCCTGTCATTAGC | 75605 |
rs3713072 | snp | A/C | 0.495868 | 0.0452663 | intron-variant | Kdm5b | GRCm38.p3 | 1:134596611 | GGTGGTATCCCTGTC[A/C]TTAGCAAGAGAAACA | 75605 |
rs3722886 | snp | A/G | 0.455 | 0.143091 | intron-variant | Kdm5b | GRCm38.p3 | 1:134610468 | CAGTTTCTGTAAAAT[A/G]TCTCTTCACATGGTT | 75605 |
rs4136473 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | GRCm38.p3 | 1:134572325 | TTTTTTTTTTTTTTC[C/T]TTTTTTTTGAGACAG | 75605 |
rs4139338 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Kdm5b | GRCm38.p3 | 1:134597913 | TGCTCTGCAGTTGAG[A/T]CCCTAGCCTATCCTC | 75605 |
rs6204707 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | Mm_Celera | 1:134603098 | aaatccgcctgcctc[C/T]ggctcccgagtgctg | 75605 |
rs6258409 | snp | A/G | 0.433884 | 0.169371 | intron-variant | Kdm5b | GRCm38.p3 | 1:134599552 | TCTTGCTCCATGTGT[A/G]TGTCTGTGTCTGTCT | 75605 |
rs6260435 | snp | C/T | 0.484429 | 0.0868505 | intron-variant | Kdm5b | GRCm38.p3 | 1:134599912 | GTGCTGATATTAATA[C/T]AGTGTAGCAAAATTT | 75605 |
rs13471821 | snp | A/G | 0.391111 | 0.206368 | synonymous-codon | Kdm5b | GRCm38.p3 | 1:134615961 | AGAATCAGAAATGAA[A/G]AAATTCCCAGACAAT | 75605 |
rs13471822 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Kdm5b | GRCm38.p3 | 1:134593415 | GCAGTCTGTGCAGCC[C/T]GCAGAAACCTGTCCT | 75605 |
rs30460592 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134572458 | AAAGGCGTGCGCCAC[C/T]GAGCCCGGCAATTTA | 75605 |
rs30467927 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | GRCm38.p3 | 1:134564930 | GGCAAACACTTAATA[C/T]GTGTAAGTCTTAAAT | 75605 |
rs30500655 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm5b | Mm_Celera | 1:134569221 | GCTAACATCTTGGTT[A/G]ATTCAGGTGTAGATT | 75605 |
rs30520012 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kdm5b | GRCm38.p3 | 1:134568065 | ATTTCTAACCCCCAA[C/T]CCTAGGATATACCTG | 75605 |
rs30557417 | snp | A/G | 0.32 | 0.24 | intron-variant | Kdm5b | GRCm38.p3 | 1:134591463 | ATTACAAATTTTTTG[A/G]TTTTGTTTTTGGAAG | 75605 |
rs30561224 | snp | A/G | 0.32 | 0.24 | intron-variant | Kdm5b | Mm_Celera | 1:134564361 | TATAGTTTATGTGCA[A/G]TGATGGGATCATTTT | 75605 |
rs30565876 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | GRCm38.p3 | 1:134578886 | TAGCTGGGAATTGAA[C/T]TCATGACCTCTGGAA | 75605 |
rs30568523 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kdm5b | Mm_Celera | 1:134593765 | GTATATAGTAATTCT[A/C]AACATAATAATCCCT | 75605 |
rs30572794 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kdm5b | Mm_Celera | 1:134624199 | GCCCCACTCACCCCC[A/G]ACCCATTGTAGTTGA | 75605 |
rs30594820 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134583754 | TCCCAGTTGGATTTG[C/T]GGGTCTACAGGAACT | 75605 |
rs30597190 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134622841 | ACCCAGCTGTGTGAT[A/C]GCTGGGCTGCTGAGC | 75605 |
rs30658667 | snp | C/G | 0.401235 | 0.199068 | intron-variant | Kdm5b | GRCm38.p3 | 1:134595714 | TTAAAAATGCGATCT[C/G]CTAAGAAAAGAATAA | 75605 |
rs30669577 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | GRCm38.p3 | 1:134609928 | CCTCTTGGAATGTGC[C/T]CTGAGTAGGAGAAAG | 75605 |
rs30672893 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kdm5b | GRCm38.p3 | 1:134570410 | TGTGGGTGCACGTAC[C/T]ATGCCAGGCCGTGGA | 75605 |
rs30700854 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134584758 | CTTGGTGGTAAGCAC[A/C]TTTACCCACTGAGCC | 75605 |
rs30703334 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | Mm_Celera | 1:134566764 | GCTAGCCTGGAATTC[C/T]CAGAGCAGTTCAGGC | 75605 |
rs30720013 | snp | C/G | 0.375 | 0.216506 | utr-variant-3-prime | Kdm5b | GRCm38.p3 | 1:134631855 | TGTTCCTTTCTTTCT[C/G]CCCTTTTCCTTTCTG | 75605 |
rs30745072 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | Mm_Celera | 1:134565567 | ACGTGTCCTGCTCTC[C/T]TGTGGAGGTCAGAGG | 75605 |
rs30747963 | snp | A/C | 0.387812 | 0.208586 | intron-variant | Kdm5b | GRCm38.p3 | 1:134623137 | GGCTCGTCTTTGGGC[A/C]GTGCAGTGTTTCTCT | 75605 |
rs30749838 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134563912 | ACCTACCTCTTTTTT[G/T]GGGGGGGCGGTGTCA | 75605 |
rs30763361 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Kdm5b | Mm_Celera | 1:134604646 | TTCTTTATGGAGTCT[A/G]TGAGGACTATCTAAG | 75605 |
rs30805623 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kdm5b | GRCm38.p3 | 1:134591370 | GGTCATTACTATTTG[C/T]CTGGTTCCATATAAT | 75605 |
rs30856970 | snp | A/G | 0.32 | 0.24 | intron-variant | Kdm5b | GRCm38.p3 | 1:134601388 | CTTGTTTATTTAGGA[A/G]CATAAGCATATCAAT | 75605 |
rs30860264 | snp | C/T | 0.18 | 0.24 | intron-variant | Kdm5b | Mm_Celera | 1:134605517 | GAAACTCTAAATTCT[C/T]CCATGTTTGTAGAGT | 75605 |
rs30860265 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Kdm5b | GRCm38.p3 | 1:134605514 | TTAGAAACTCTAAAT[C/T]CTCCCATGTTTGTAG | 75605 |
rs30860266 | snp | A/T | 0.456747 | 0.140554 | intron-variant | Kdm5b | GRCm38.p3 | 1:134605488 | TGAGTCAAATGTGAT[A/T]CCTTATCTTTTTAGA | 75605 |
rs30860267 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134605354 | AGGGTTGTTTAGAAA[C/T]AATTGCCTTATTCGT | 75605 |
rs30860268 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Kdm5b | GRCm38.p3 | 1:134605224 | GCACTTGGATGGTCA[A/G]CATGATTGTGCTTCC | 75605 |
rs30860269 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134605194 | ACAGAAAATGTACCA[C/T]AAGAACGAGAGCTGG | 75605 |
rs30860270 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kdm5b | Mm_Celera | 1:134604303 | CCTTCTGACCTCCTT[A/G]TACTTGTCCACATGA | 75605 |
rs30860271 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Kdm5b | GRCm38.p3 | 1:134604066 | ACGTGTGCAGCTTGA[C/T]CAGTCCTCACACACG | 75605 |
rs30860272 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134604052 | AGAGAAGTGTATACA[C/G]GTGTGCAGCTTGATC | 75605 |
rs30860273 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Kdm5b | GRCm38.p3 | 1:134603938 | GTCCTGCTTTTCATG[C/G]AGCTGGCTTCCTGAA | 75605 |
rs30860294 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Kdm5b | Mm_Celera | 1:134589590 | ACAGTGCAATGCTAA[A/T]TCTTAAATCATGGCG | 75605 |
rs30860295 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kdm5b | GRCm38.p3 | 1:134589337 | TGCTGCAAAGCACGG[C/T]CCTCTCCCAGCTGTT | 75605 |
rs30860296 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | Mm_Celera | 1:134588338 | TCCAGTTCTGGGTTC[C/T]ACTTCATTTTACCAC | 75605 |
rs30860297 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kdm5b | Mm_Celera | 1:134588298 | GGAAGTTGAAAAGAC[A/G]TTAGCTGCAAAGGCT | 75605 |
rs30860298 | snp | A/T | 0.415225 | 0.187619 | intron-variant | Kdm5b | Mm_Celera | 1:134588263 | ATTTTAGTTTAAATC[A/T]GGAAGAACCTAAAGC | 75605 |
rs30860299 | snp | C/T | 0.493827 | 0.0552116 | intron-variant | Kdm5b | Mm_Celera | 1:134588242 | TCACTGCAAAGGGTC[C/T]TTCCCATTTTAGTTT | 75605 |
rs30860300 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134588137 | ATTGGTAAAATGAGA[C/T]TTTTTTCTTGTTGTT | 75605 |
rs30860301 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kdm5b | Mm_Celera | 1:134587870 | GATGACCTTGTTCAC[A/G]GCCACAGGGAAAGCC | 75605 |
rs30860302 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134587501 | CTATAGTGATTCTTA[A/G]TTGAGACATTGTTCA | 75605 |
rs30860303 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Kdm5b | GRCm38.p3 | 1:134587472 | TTATTTTAACCAATA[A/G]CATTAAATTGTGCCT | 75605 |
rs30861144 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134587196 | TAGAGGACATAGAGG[A/T]ATAGAGGACAGCTCG | 75605 |
rs30861145 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Kdm5b | GRCm38.p3 | 1:134585765 | CTTTTTGGTTTCTAT[A/G]CTGTAGAAAGTGGTT | 75605 |
rs30861146 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Kdm5b | GRCm38.p3 | 1:134585540 | ACACTTAAAACTTTC[A/G]TTTAATTTTTAATTT | 75605 |
rs30861147 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134585425 | GTAATACATATGAGT[A/T]ATCGTATCTTTAGAT | 75605 |
rs30861148 | snp | A/G | 0.32 | 0.24 | intron-variant | Kdm5b | GRCm38.p3 | 1:134585277 | GATGAGTCTGCCACT[A/G]ACTAATGTCACAGTC | 75605 |
rs30861149 | snp | A/C | 0.132653 | 0.220748 | synonymous-codon, utr-variant-5-prime | Kdm5b | Mm_Celera | 1:134585205 | CTTCATTTCACCCCG[A/C]GGATCCAGAGGCTGA | 75605 |
rs30861150 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134585119 | TAATTTCAAGTGTTA[A/G]GTTATTATATCTAAT | 75605 |
rs30861151 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Kdm5b | GRCm38.p3 | 1:134585022 | ATGCCGGATGTACCA[A/G]TGTCTTGGGTGGATT | 75605 |
rs30861152 | snp | A/T | 0.33241 | 0.236027 | intron-variant | Kdm5b | GRCm38.p3 | 1:134584962 | CCAACTTAGGTAAAA[A/T]TGATTCTGAAGTATC | 75605 |
rs30861153 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kdm5b | GRCm38.p3 | 1:134584304 | TTTAGGTATTAAAGT[C/T]ATCTTCCTGTTTCTT | 75605 |
rs30861204 | snp | A/T | 0.432133 | 0.171253 | intron-variant | Kdm5b | GRCm38.p3 | 1:134603914 | TATTTAATTTTCATA[A/T]TTGTAAGTGTCCTGC | 75605 |
rs30861205 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134603834 | ACTGAGGTGGTGAGG[A/C]AAAGCCACTGCTGCC | 75605 |
rs30861206 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kdm5b | Mm_Celera | 1:134603542 | CTTTTATTAGATATT[C/T]TTAATTGAATTTATT | 75605 |
rs30861207 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Kdm5b | Mm_Celera | 1:134603509 | ATCTGACTAGGAGAG[C/T]AGAACATCTTTATTT | 75605 |
rs30861208 | snp | A/C | 0.5 | 0 | intron-variant | Kdm5b | GRCm38.p3 | 1:134602673 | GCACAGCCTTGGACT[A/C]GTGACATCCTCACTA | 75605 |
rs30861209 | snp | C/T | 0.5 | 0 | intron-variant | Kdm5b | GRCm38.p3 | 1:134602664 | GTGTCGAAAGCACAG[C/T]CTTGGACTCGTGACA | 75605 |
rs30861210 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Kdm5b | GRCm38.p3 | 1:134602424 | TGAATGAAAAAATTC[C/T]TCTTTTAATTTCCTT | 75605 |
rs30861211 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Kdm5b | Mm_Celera | 1:134602354 | ATTATGAACAGATTT[C/T]TTTGCTTAGAAGTTT | 75605 |
rs30861212 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134601696 | AGTCATGTTTAACTG[G/T]CTTATGATATTTCTT | 75605 |
rs30861213 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134601433 | GTCAAAATTAAATGG[A/T]TTCCAGCGTGATTCT | 75605 |
rs30861574 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kdm5b | Mm_Celera | 1:134601383 | TACTCCTTGTTTATT[C/T]AGAAACATAAGCATA | 75605 |
rs30861575 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kdm5b | Mm_Celera | 1:134601259 | CACTGGTGGAAAGCT[C/T]GCTGTGTATCAAGTA | 75605 |
rs30861576 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kdm5b | GRCm38.p3 | 1:134601253 | TCACAACACTGGTGG[A/G]AAGCTCGCTGTGTAT | 75605 |
rs30861577 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Kdm5b | GRCm38.p3 | 1:134601108 | AAGAGTTAATATGGA[C/T]AGTGTATAGACAGTT | 75605 |
rs30861578 | snp | C/G | 0.429688 | 0.173817 | intron-variant | Kdm5b | GRCm38.p3 | 1:134601030 | GCCACTAGCACACCT[C/G]GACTAATTACACCTT | 75605 |
rs30861579 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Kdm5b | Mm_Celera | 1:134601022 | CCTACAGGGCCACTA[C/G]CACACATGGACTAAT | 75605 |
rs30861580 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Kdm5b | Mm_Celera | 1:134600849 | AATCAAAGACACCGT[A/G]TAGAAGTTGGTTCTT | 75605 |
rs30861581 | snp | A/G | 0.401235 | 0.199068 | synonymous-codon | Kdm5b | GRCm38.p3 | 1:134600699 | CTATACACTTCGTAC[A/G]TTTGGAGAAATGGCA | 75605 |
rs30861582 | snp | C/T | 0.415225 | 0.187619 | synonymous-codon | Kdm5b | GRCm38.p3 | 1:134600663 | ACAAGAAGCTTTTGG[C/T]TTTGAACAAGCAGCA | 75605 |
rs30861583 | snp | C/G | 0.493827 | 0.0552116 | missense | Kdm5b | Mm_Celera | 1:134600656 | ATAAGCCACAAGAAG[C/G]TTTTGGTTTTGAACA | 75605 |
rs30861834 | snp | G/T | 0.396694 | 0.202437 | intron-variant | Kdm5b | GRCm38.p3 | 1:134584277 | ATTTTATCCTTTCAG[G/T]TGCACCCTTATTTTA | 75605 |
rs30861835 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Kdm5b | GRCm38.p3 | 1:134581993 | AGGGGTTACAATCAG[A/G]GTAACTGTGCTCAGC | 75605 |
rs30861836 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kdm5b | Mm_Celera | 1:134581479 | CAAAGCTCTGAACAC[A/G]TCTTTCTCTTACTTC | 75605 |
rs30861837 | snp | C/T | 0.42 | 0.183303 | intron-variant | Kdm5b | Mm_Celera | 1:134581440 | CTTTCTGAAAGCCAG[C/T]AGCTTTTGTAAAGTA | 75605 |
rs30861838 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Kdm5b | Mm_Celera | 1:134581201 | GACCCATATGTCTTA[A/G]CTTTTCTGATACATT | 75605 |