SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs31417521 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5d | Mm_Celera | Y:915138 | GGTCTCAAGTTAACT[C/T]AGTCATTGTTTGGCT | 20592 |
rs45720222 | snp | C/T | 0.197531 | 0.244432 | upstream-variant-2KB | Kdm5d | Mm_Celera | Y:897558 | CTGCGCAGGCGCTCG[C/T]GTGCAGTGATATCTT | 20592 |
rs45857394 | snp | A/G | | | intron-variant | Kdm5d | Mm_Celera | Y:932182 | GAATATGTCTAATAC[A/G]CTAGCCTTTCCTGTG | 20592 |
rs45965717 | snp | A/T | | | intron-variant | Kdm5d | Mm_Celera | Y:912062 | TTGTTTTTTGTTTTT[A/T]ATTTTTTTGTTTTTT | 20592 |
rs45997197 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5d | Mm_Celera | Y:936826 | CAAGTTTGTATTTTA[C/T]AGAAAGGCATTGGCA | 20592 |
rs46022299 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Kdm5d | Mm_Celera | Y:912881 | AACCATTTCTGACTT[A/T]TGTTTGATGGTATTT | 20592 |
rs46199297 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kdm5d | Mm_Celera | Y:913414 | AGAGTAGCTAGTTGT[A/G]GTGAATGAATGGGAA | 20592 |
rs46279114 | snp | A/G | 0.18 | 0.24 | intron-variant | Kdm5d | Mm_Celera | Y:899635 | AGAAAGGAGTACAAT[A/G]TAACCTGGCAACAAC | 20592 |
rs47073483 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kdm5d | Mm_Celera | Y:935748 | TACTGTGGGCAGGAA[C/T]GGTCAGAGTGGGTCA | 20592 |
rs47082795 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm5d | Mm_Celera | Y:909484 | ATGATACAGGGGAGA[A/G]GAATTACGTTTTTAA | 20592 |
rs47535292 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kdm5d | Mm_Celera | Y:913364 | AAATTCTGATGTTTT[C/T]TTAGAGAATTGACCA | 20592 |
rs47616285 | snp | A/G | | | intron-variant | Kdm5d | Mm_Celera | Y:932017 | ATCTAAAGGGGTTAA[A/G]TGTGACTCCACAACT | 20592 |
rs47853585 | snp | A/G | | | intron-variant | Kdm5d | Mm_Celera | Y:932119 | CAACTTGAAATCTAA[A/G]GTCTGGTAATGTCTG | 20592 |
rs48295818 | snp | C/T | | | intron-variant | Kdm5d | Mm_Celera | Y:932125 | TAGGGGCAGACATTA[C/T]CAGACCTTAGATTTC | 20592 |
rs48314714 | snp | G/T | | | intron-variant | Kdm5d | Mm_Celera | Y:917637 | GTGCATATATATATA[G/T]AGAGGGGGGGGGGAC | 20592 |
rs48685451 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, utr-variant-5-prime | Kdm5d | Mm_Celera | Y:916679 | TTTTGGCTTTGAGCA[A/G]GCTACACAGGAGTAT | 20592 |
rs48834187 | snp | A/G | 0.48 | 0.0979796 | synonymous-codon, utr-variant-5-prime | Kdm5d | Mm_Celera | Y:916757 | CTTCAACATGCCTGT[A/G]CATGTATGTGACTGA | 20592 |
rs49184318 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm5d | Mm_Celera | Y:910134 | GAATTGTTGGTAGTG[A/G]TGGTTGTTATATTAT | 20592 |
rs49571988 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Kdm5d | Mm_Celera | Y:909883 | ATTATCTTTTTCACA[A/G]CAAGAAAAAATGGGA | 20592 |
rs49587541 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Kdm5d | Mm_Celera | Y:909854 | CCCTTCTCCAATCTT[A/G]AAAACAATATTTAAT | 20592 |
rs49846352 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kdm5d | Mm_Celera | Y:898962 | TATTTCTTTTTTAAG[A/G]TTACTTACATCCTTC | 20592 |
rs49889345 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Kdm5d | Mm_Celera | Y:899697 | TGATATTTGAAGGAC[A/T]TGCTATGTTTCCTGC | 20592 |
rs50243220 | snp | G/T | | | intron-variant | Kdm5d | Mm_Celera | Y:932124 | TGAAATCTAAGGTCT[G/T]GTAATGTCTGCCCCT | 20592 |
rs50718171 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Kdm5d | Mm_Celera | Y:938389 | CTTTCTAGCACTTGT[G/T]ACTTTCCTATATACT | 20592 |
rs50786350 | snp | A/G | | | intron-variant | Kdm5d | Mm_Celera | Y:930753 | CTCCTTAGGCTGTGG[A/G]AAATACAGGGATGAG | 20592 |
rs51486078 | snp | A/G | | | synonymous-codon | Kdm5d | Mm_Celera | Y:939861 | AGTTATAATACGTGA[A/G]GCAGAAAACATCCCT | 20592 |
rs51883043 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kdm5d | Mm_Celera | Y:911185 | TATAATAATATTTCA[A/G]AGCTATGATTCTGTA | 20592 |
rs52187476 | snp | A/G | 0.18 | 0.24 | upstream-variant-2KB | Kdm5d | Mm_Celera | Y:896497 | GCTTGTTCAGCATAA[A/G]TAGTGGAATTCTTTG | 20592 |
rs52221093 | snp | C/G | 0.18 | 0.24 | missense, utr-variant-5-prime | Kdm5d | Mm_Celera | Y:900594 | GCTACAGTAGACGAG[C/G]AAAAAGGCTACAGCC | 20592 |
rs52347214 | snp | G/T | | | intron-variant | Kdm5d | GRCm38.p3 | Y:918057 | ATGAGTATTTCAAGG[G/T]ATCTCTCTCCCTCTC | 20592 |
rs107872904 | snp | C/T | | | intron-variant | Kdm5d | Mm_Celera | Y:930792 | ACCTTGCAGTAACAG[C/T]AAGGGTGAAAAGCCA | 20592 |
rs108020507 | snp | A/C | | | intron-variant | Kdm5d | Mm_Celera | Y:932028 | TTAAGTGTGACTCCA[A/C]AACTGTGTCCAGTAA | 20592 |
rs108186827 | snp | A/C | | | intron-variant | Kdm5d | Mm_Celera | Y:931920 | GACGCCAGTAAGAAA[A/C]CTGCTGCTTCTAACG | 20592 |
rs108371084 | snp | C/T | | | intron-variant | Kdm5d | Mm_Celera | Y:932135 | GTCTGGTAATGTCTG[C/T]CCCTAGTATCTTGCT | 20592 |
rs108423256 | snp | A/G | | | intron-variant | Kdm5d | Mm_Celera | Y:929905 | GTTTACCATAAGAAA[A/G]GTTATAGAATCCCAG | 20592 |
rs108507178 | snp | C/T | | | intron-variant | Kdm5d | Mm_Celera | Y:930754 | TCATCCCTGTATTTT[C/T]CACAGCCTAAGGACA | 20592 |
rs108597441 | snp | C/T | | | intron-variant | Kdm5d | Mm_Celera | Y:932163 | GCTGATCAACTACCT[C/T]GACCACCGGAAAGGC | 20592 |
rs108604524 | snp | C/G | | | intron-variant | Kdm5d | Mm_Celera | Y:931919 | ACGCCAGTAAGAAAA[C/G]TGCTGCTTCTAACGC | 20592 |
rs108764567 | snp | C/T | | | intron-variant | Kdm5d | Mm_Celera | Y:932170 | AACTACCTCGACCAC[C/T]GGAAAGGCTAGCGTA | 20592 |
rs108890199 | snp | C/T | | | intron-variant | Kdm5d | Mm_Celera | Y:930734 | GAGCTGGAAGTCGTT[C/T]CTCCTCATCCCTGTA | 20592 |
rs864295890 | snp | G/T | | | synonymous-codon | Kdm5d | GRCm38.p3 | Y:927736 | AGCTGAGCGAGAGGC[G/T]TTTGAGCTACTCCCA | 20592 |
rs864299483 | in-del | -/A | | | utr-variant-3-prime | Kdm5d | GRCm38.p3 | Y:943728 | AGGAATATATACAGT[-/A]ATGCAAACTTACCAT | 20592 |