SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3090516 | snp | A/C | 0.21875 | 0.248039 | utr-variant-3-prime | Kmt2a | GRCm38.p3 | 9:44807242 | GGAGCGGCTCCCTCT[A/C]CATCCCTTCTCTTTA | 214162 |
rs3710352 | snp | C/T | 0.5 | 0 | intron-variant | Kmt2a | Mm_Celera | 9:44858752 | GTTGGTCTAAGTTGG[C/T]ATCATTATACTTGGT | 214162 |
rs3710371 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44858756 | GTCTAAGTTGGCATC[A/G]TTATACTTGGTTCAA | 214162 |
rs3715124 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kmt2a | Mm_Celera | 9:44862301 | GAAAACACATCTGAT[A/G]TGATGAACATGGAAG | 214162 |
rs3717187 | snp | A/G | 0.433884 | 0.169371 | intron-variant | Kmt2a | Mm_Celera | 9:44862660 | AAAATTACTTTTGAG[A/G]AGAGACAAACACCCA | 214162 |
rs3717207 | snp | C/G | 0.408163 | 0.193609 | intron-variant | Kmt2a | Mm_Celera | 9:44862672 | GAGGAGAGACAAACA[C/G]CCATCCGCACAAGAC | 214162 |
rs4137386 | snp | A/C | 0.415225 | 0.187619 | intron-variant | Kmt2a | Mm_Celera | 9:44858716 | ACTCACTTTGTGAGA[A/C]ACTTGCTTTCAGGCA | 214162 |
rs6286374 | snp | C/T | 0.5 | 0 | intron-variant | Kmt2a | Mm_Celera | 9:44823887 | TTCTGAAGAGGGAGA[C/T]Gtagggctctccctg | 214162 |
rs6286460 | snp | A/G | 0.5 | 0 | intron-variant | Kmt2a | Mm_Celera | 9:44823936 | aacttacagagatcc[A/G]tctgcctctgctccc | 214162 |
rs6286955 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Kmt2a | Mm_Celera | 9:44824041 | CTTGTCAAGTACTTC[A/G]ACAATTTAATTCACA | 214162 |
rs6288014 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44824195 | CACAGGGACTGTGAG[C/T]GTTAGAACAGCCTGC | 214162 |
rs13473595 | snp | G/T | | | utr-variant-3-prime, upstream-variant-2KB | Kmt2a, Ttc36 | Mm_Celera | 9:44804444 | ACCAAGTTGTTTTtt[G/T]ttgttattgttgttg | 214162 |
rs13480168 | snp | A/G | 0.486523 | 0.0809756 | synonymous-codon | Kmt2a | Mm_Celera | 9:44849633 | CTTTATCCGTTCTGT[A/G]GATGGAGGCCTTCCT | 214162 |
rs29586282 | snp | C/T | 0.5 | 0 | intron-variant | Kmt2a | Mm_Celera | 9:44863770 | AGTTGACCTTGAACC[C/T]CCAACACAGTTTACC | 214162 |
rs29588155 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Kmt2a | GRCm38.p3 | 9:44826888 | ATCATCTTCAAACAC[C/T]TCTGCTGACCACAAA | 214162 |
rs29588881 | snp | C/G | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44814841 | CCTGTGGGTCCCAAA[C/G]GACCCTTTCACAGGG | 214162 |
rs29590060 | snp | A/G | 0.387812 | 0.208586 | utr-variant-3-prime, upstream-variant-2KB | Kmt2a, Ttc36 | GRCm38.p3 | 9:44804032 | CTGCACGCTCCTCTC[A/G]GGACAGGCGGGCGTC | 214162 |
rs29590516 | snp | A/C | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44814439 | TGAGAGAGCAGCTCT[A/C]AGTGTGTACCACACA | 214162 |
rs29592372 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Kmt2a | Mm_Celera | 9:44817029 | CTGGAAGCATCCTAA[C/T]TACTTTGCCATTTCT | 214162 |
rs29592664 | snp | A/G | 0.5 | 0 | intron-variant | Kmt2a | Mm_Celera | 9:44865413 | TGTCAGAGGCCAGGG[A/G]AAAGAGAAGGGGGTG | 214162 |
rs29593585 | snp | A/G | 0.429688 | 0.173817 | synonymous-codon | Kmt2a | GRCm38.p3 | 9:44822041 | TGGTGTCAGTTTAGG[A/G]ATTCCAGGGTAAGCT | 214162 |
rs29594849 | snp | G/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Kmt2a, Gm30816 | Mm_Celera | 9:44873435 | GAATGTGTGGTTAAC[G/T]TCTCGAGTTTTTACA | 214162 |
rs29595314 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Kmt2a | Mm_Celera | 9:44836284 | TTACACCGCCCTCCC[C/T]GCCAAGACACGCCAG | 214162 |
rs29596451 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Kmt2a | Mm_Celera | 9:44808562 | ATCATACCTGGCTGA[A/G]CTTGTCATCACTCAG | 214162 |
rs29636455 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Kmt2a | Mm_Celera | 9:44866575 | AGTGGCCAGCGGGGG[A/T]GAGAGCCGATTCTCT | 214162 |
rs29638298 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kmt2a | Mm_Celera | 9:44845343 | CCAGGTTGTCACCCC[A/G]TGTGACAAACCGTGA | 214162 |
rs29640653 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Kmt2a | Mm_Celera | 9:44855950 | TGATTTCTTGACTAC[A/G]CTTTAAAGTAAAAGT | 214162 |
rs29641889 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44812190 | TGCTGGGATTAAAGG[C/T]GTGCGCCCGGCACCA | 214162 |
rs29642107 | snp | C/T | 0.42 | 0.183303 | intron-variant | Kmt2a | Mm_Celera | 9:44868748 | GGCGGCGGGAAGACG[C/T]CTGGTGTGAGTATTA | 214162 |
rs29642245 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44864023 | CCGCACAGTTGACCT[C/G]TAGCCCCCACACAGC | 214162 |
rs29646038 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Kmt2a | Mm_Celera | 9:44827272 | AGGGCTTCATGTGGG[C/T]AGAAACTCTAATACC | 214162 |
rs29647624 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44809686 | TGGAAAAATGTTAGT[G/T]TTCTCAAATTCTACA | 214162 |
rs29650040 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44866815 | CTAGTTTCCAAGCTT[C/T]TAATTCAGTTCTACC | 214162 |
rs29650897 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Kmt2a | Mm_Celera | 9:44858188 | CATCATTAATACGTG[C/T]TACACAGCCCACACG | 214162 |
rs29651217 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44830792 | ACTCAAATGAAGAAC[C/T]AACTCAATAGTAAGT | 214162 |
rs29684097 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44857938 | CCTCTCTATCTCATC[C/T]CACTTACAAGTGGGG | 214162 |
rs29691705 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kmt2a | Mm_Celera | 9:44817379 | ACTTGGAACACAGCA[C/T]GCATGCATGTCAGCC | 214162 |
rs29692443 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Kmt2a | Mm_Celera | 9:44859971 | TTTGGCTCTAATGGA[A/G]GAATGAGTTTAGGTG | 214162 |
rs29692723 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44866530 | AAAGGAAAAAAAAAA[A/C]GTAACTGAACTAACA | 214162 |
rs29694148 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44836759 | ATAATAACCATCGTC[C/T]ATACATCCTGTGGGT | 214162 |
rs29695659 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44851266 | CTGAAAATGCACCAA[A/G]AACTGGCTCCAGCAG | 214162 |
rs29739668 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Kmt2a | Mm_Celera | 9:44835057 | ACTGACAGGAGCATG[C/T]CACCTGCACTCTAAG | 214162 |
rs29740289 | snp | A/G | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Kmt2a, Gm30816 | Mm_Celera | 9:44872657 | GTGTAGCTGTCCTTC[A/G]GTTTGGTTCCACTTA | 214162 |
rs29741644 | snp | G/T | 0.387812 | 0.208586 | intron-variant | Kmt2a | Mm_Celera | 9:44835971 | TCTTGGGCTAGCGTC[G/T]TCTGTTATTTCAAAG | 214162 |
rs29744696 | snp | A/G | 0.429688 | 0.173817 | synonymous-codon | Kmt2a | GRCm38.p3 | 9:44824537 | TATCATCATGTGGAT[A/G]TTTTCTGGTTCCAAG | 214162 |
rs29744891 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Kmt2a | Mm_Celera | 9:44851719 | CAGTAGATAACACTT[C/T]ATTTAAGCAATATAT | 214162 |
rs29746576 | snp | A/G | 0.429688 | 0.173817 | synonymous-codon | Kmt2a | GRCm38.p3 | 9:44818855 | AGGCTGGTCCTGAAT[A/G]CCCAGGCTCTGGTGG | 214162 |
rs29782321 | snp | A/T | 0.455 | 0.143091 | intron-variant | Kmt2a | Mm_Celera | 9:44850779 | GTTCTGGTAGAGTAA[A/T]CTAAGAAAGGCTTAC | 214162 |
rs29786430 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Kmt2a | Mm_Celera | 9:44830682 | ACAATTAACTCGAGC[C/T]AATCAAGAGTTGCCA | 214162 |
rs29787065 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44811957 | CCGAGGATCAGAAGG[A/G]GATTAGGGTGGAATA | 214162 |
rs29790229 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44854385 | CGGGTGGTTGTGAGC[C/T]ACCATGTGGTTGCTG | 214162 |
rs29795202 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44854595 | TACACAAACGTAAGT[A/G]CAGGCAAAATATCTA | 214162 |
rs29826480 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44837816 | ACCAAACAAAGAAAC[A/G]CCCTGTTTTTATTAC | 214162 |
rs29834245 | snp | C/T | 0.42 | 0.183303 | intron-variant | Kmt2a | Mm_Celera | 9:44850823 | CTACTCACGAGACAT[C/T]GGCACAATCACCAGC | 214162 |
rs29835306 | snp | C/G | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44826606 | CTCACAGGGTTTATT[C/G]TCTGACCTTCAGAGT | 214162 |
rs29837259 | snp | C/T | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Kmt2a, Gm30816 | Mm_Celera | 9:44873911 | AACTAACAACTACAT[C/T]GATACCACTGTTAAA | 214162 |
rs29839209 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44859500 | CATAATGAGATAGCG[A/G]TTTACAGCTATTAGA | 214162 |
rs29841687 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Kmt2a | Mm_Celera | 9:44829926 | AAAAGTCCCAGGCTA[C/T]GCCAAACACAAATGT | 214162 |
rs29841908 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44863559 | AGTTCAATCCCTAGC[A/G]ACCACGTGATGGCCC | 214162 |
rs29845315 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44812195 | GGATTAAAGGCGTGC[A/G]CCCGGCACCACGCCC | 214162 |
rs29880160 | snp | A/T | 0.455 | 0.143091 | intron-variant, upstream-variant-2KB | Kmt2a, Gm30816 | Mm_Celera | 9:44870213 | CTCATGTGAGCATGC[A/T]AAGGGCAAACATTCT | 214162 |
rs29881136 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44815943 | AGCCCAGGTTGGCTT[C/T]AAACTCGTGCCAACC | 214162 |
rs29882410 | snp | C/T | 0.455 | 0.143091 | intron-variant | Kmt2a | Mm_Celera | 9:44856171 | AGAAGAGGTCTTCAC[C/T]GCTGCACACTACACT | 214162 |
rs29886050 | snp | A/T | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44855753 | TGCTGGCACGGTGGC[A/T]CATGCCCTTAATCCT | 214162 |
rs29892875 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44811605 | ATATGGGGCTGCTTC[A/G]GTGTGTTCATAGCTC | 214162 |
rs29919281 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Kmt2a | Mm_Celera | 9:44851237 | AAACTTCCCCTAACA[C/T]CTAACAGCTTGCACT | 214162 |
rs29925770 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Kmt2a | Mm_Celera | 9:44834040 | AAGCCAAGGTTGCAG[C/T]CTGCTGTGGCCCACA | 214162 |
rs29926750 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Kmt2a | Mm_Celera | 9:44861534 | GGATGCAGCTCTCAG[C/T]CACTGCTCCAGTGTC | 214162 |
rs29926822 | snp | C/G | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44826597 | ACACGTGTGCTCACA[C/G]GGTTTATTCTCTGAC | 214162 |
rs29927523 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Kmt2a | Mm_Celera | 9:44850923 | GGCTTCTCAAACTAG[A/G]TAGTCCCTAGTCCCT | 214162 |
rs29929572 | snp | A/G | 0.387812 | 0.208586 | intron-variant | Kmt2a | Mm_Celera | 9:44830217 | TCTCAGGCCAAGGCA[A/G]AGACCCACTTATGCT | 214162 |
rs29931609 | snp | A/T | 0.387812 | 0.208586 | intron-variant | Kmt2a | Mm_Celera | 9:44859610 | CCAGAACAGCTATTT[A/T]AAAAAATGGCATGGC | 214162 |
rs29933695 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44812806 | ATGGACAGATATACT[A/G]AAAACCACTGAACTG | 214162 |
rs29936022 | snp | C/T | 0.5 | 0 | intron-variant | Kmt2a | Mm_Celera | 9:44834696 | GGACTCTTCCTTTGG[C/T]TGTTCTCCCTCATAT | 214162 |
rs29937802 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Kmt2a | GRCm38.p3 | 9:44848124 | TGCTCTCTGATTTTT[C/T]TCTGTAGATTCCCCA | 214162 |
rs29941678 | snp | C/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Kmt2a, LOC105243391, Gm30816 | Mm_Celera | 9:44879618 | AACTTGGCTTCATAA[C/T]CCTCCTCTTTCTCCC | 214162 |
rs29942491 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44856820 | AGAATTCACTACTCG[C/T]AGCCATAACTATAGG | 214162 |
rs29942700 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Kmt2a | Mm_Celera | 9:44855922 | TTTGTTTTGTTGCAT[C/T]TGAAATATATACTGA | 214162 |
rs29944005 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Kmt2a | Mm_Celera | 9:44853572 | GATGGCGACAGGAAT[A/C]GTAAACTGACCACAC | 214162 |
rs29944331 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime, upstream-variant-2KB | Kmt2a, Ttc36 | GRCm38.p3 | 9:44803825 | AAAGAAACACCACAA[A/G]TCTATTTTTTTTTCT | 214162 |
rs29961320 | snp | C/T | 0.444444 | 0.157135 | intron-variant, nc-transcript-variant | Kmt2a, Gm30816 | Mm_Celera | 9:44872522 | GCAACTCCTATGCAG[C/T]TGCCTGGGCCGGACC | 214162 |
rs29974217 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Kmt2a | Mm_Celera | 9:44824910 | AGAAAGGCTACTAAC[C/T]GCAAGATTCCAACCA | 214162 |
rs29976191 | snp | A/G | 0.42 | 0.183303 | intron-variant | Kmt2a | Mm_Celera | 9:44838940 | ACCAGGCATTTGCAG[A/G]CTGAATAGTCTCAGC | 214162 |
rs29979949 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44833618 | GCATATGGCTCTATG[G/T]GTAGGGTCCTGAACT | 214162 |
rs29981133 | snp | A/G | 0.444444 | 0.157135 | missense | Kmt2a | GRCm38.p3 | 9:44822070 | CTGTGCTATGTGCAG[A/G]TCCATCTGTGCTCTT | 214162 |
rs29988881 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44812172 | CTGCCTCTGCCTCCC[A/G]AGTGCTGGGATTAAA | 214162 |
rs29990148 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kmt2a | Mm_Celera | 9:44842140 | AAAGCTAAGAGACCA[A/G]AAAACAAAACACCAA | 214162 |
rs29990484 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Kmt2a | Mm_Celera | 9:44816412 | TCGAGCCTACTATGT[C/G]ATGTAGCACAGGCTG | 214162 |
rs29991787 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Kmt2a | Mm_Celera | 9:44845328 | GTCAGTGCAAGCACA[C/G]CAGGTTGTCACCCCA | 214162 |
rs29992170 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44859873 | AGCACTCGCTTACAC[A/G]TGGCATCTAAAGGGA | 214162 |
rs30026012 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Kmt2a | Mm_Celera | 9:44866406 | AATGTAAGTACTAAA[A/G]TAATTATAGCACTTT | 214162 |
rs30027998 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kmt2a | Mm_Celera | 9:44857932 | CACATACCTCTCTAT[C/T]TCATCCCACTTACAA | 214162 |
rs30029134 | snp | A/G | 0.48 | 0.0979796 | intron-variant, nc-transcript-variant | Kmt2a, Gm30816 | Mm_Celera | 9:44874535 | CTGCAAGAACAAAAT[A/G]GCCCTCTGTCTGCCC | 214162 |
rs30031519 | snp | C/T | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44856667 | TCCTGGAGGCTAGGC[C/T]GCTTAGAGTTCAGCA | 214162 |
rs30033091 | snp | A/T | 0.465374 | 0.126941 | intron-variant | Kmt2a | Mm_Celera | 9:44817835 | ATCAGCAAAGACACA[A/T]TGGACAGATAAAGTT | 214162 |
rs30038380 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Kmt2a | GRCm38.p3 | 9:44806184 | GAGGGAGGGGGCAAT[A/G]CAGCAAAGAGGAGGA | 214162 |
rs30038528 | snp | C/T | 0.455 | 0.143091 | intron-variant | Kmt2a | Mm_Celera | 9:44868796 | AGTAATCTAGATGAA[C/T]AATCCCAACTTCACA | 214162 |
rs30039719 | snp | C/T | 0.5 | 0 | intron-variant, upstream-variant-2KB, nc-transcript-variant | Kmt2a, LOC105243391, Gm30816 | Mm_Celera | 9:44879681 | CTAAGGCAAAACTGT[C/T]CTTTTATCTACTCTC | 214162 |
rs30041051 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kmt2a | Mm_Celera | 9:44850985 | GAAGGCAAAGCAACA[A/G]TTTATTAAGACAGAT | 214162 |
rs30043186 | snp | C/G | 0.432133 | 0.171253 | intron-variant | Kmt2a | Mm_Celera | 9:44814319 | CTGTACGAGGCAGAC[C/G]AGGTGGAGCTGGCAG | 214162 |