SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6339933 | snp | A/T | 0.375 | 0.216506 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114379135 | AGGTGATTCCGATAC[A/T]AAGGAGGATTAGACA | 330171 |
rs6352876 | snp | A/C | 0.345679 | 0.230967 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114379198 | GGGAGCTCTTCCGGG[A/C]GGGTTGCTTAAGGGG | 330171 |
rs6353928 | snp | G/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114379385 | AAACAGTCTCAATGA[G/T]GATGTTGTCAATCCT | 330171 |
rs6354976 | snp | C/G | 0.486111 | 0.0821678 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114379567 | CAGTTGGTGGTCTAC[C/G]GGTGCTGCTGGCCGC | 330171 |
rs13468560 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Kctd10 | GRCm38.p3 | 5:114375050 | GGCTGCCACCCGCAC[C/T]ACTTCCTTCAAGGGT | 330171 |
rs29506512 | snp | A/G | 0.188366 | 0.242283 | intron-variant | Kctd10 | Mm_Celera | 5:114366214 | TTGCAAAGCTATTCT[A/G]GGTATCCGACTTCCT | 330171 |
rs29511015 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kctd10 | Mm_Celera | 5:114374487 | TTCATTTCCACAAAC[A/G]CCCTACAGTGCGGGT | 330171 |
rs29522020 | snp | C/T | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114367081 | GTGCAAACCTGAATC[C/T]GGCCAGATTGCCCGG | 330171 |
rs29527093 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114373699 | GAGGACAAGCATGTG[G/T]GTGCTCGTTCACAGA | 330171 |
rs29542370 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Kctd10 | Mm_Celera | 5:114372070 | AAAGCTCTGGCAATA[A/C]TCAGCACAGTGGAAG | 330171 |
rs29544681 | snp | C/T | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114373707 | GCATGTGGGTGCTCG[C/T]TCACAGAAGCCAGCC | 330171 |
rs29546203 | snp | C/T | 0.465374 | 0.126941 | utr-variant-3-prime | Kctd10, Myo1h | Mm_Celera | 5:114363601 | AACGTTTATTTTACA[C/T]ATGTCCGCAGACACT | 330171 |
rs29546525 | snp | A/C | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114378685 | AAGCTGAGGGAAACA[A/C]GCCGATGGTGGAGCC | 330171 |
rs29550849 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114367606 | GCCCCTAACCCACGG[G/T]GGCACATCTGCTCCA | 330171 |
rs29564181 | snp | C/T | 0.188366 | 0.242283 | utr-variant-3-prime | Kctd10, Myo1h | Mm_Celera | 5:114363848 | CTGGGCCAGACCTGC[C/T]AGGCTGTGGGCCCCA | 330171 |
rs29566996 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114371763 | CTGGGGAAAGTTCCA[C/T]GCAAACAGAGCCCAC | 330171 |
rs29580203 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kctd10 | Mm_Celera | 5:114372451 | ATGACACTTACAAAC[C/T]TGCCTGTATGCCGGA | 330171 |
rs29580535 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Kctd10 | GRCm38.p3 | 5:114377125 | TGTGTACGTTTGTGT[A/G]GACACTCGGCATATA | 330171 |
rs29580729 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114373145 | AAGGGTAAGATGGGA[C/T]CCCCGTCCTCCCGTT | 330171 |
rs29582011 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114372180 | TCCCGACCCTTGTCC[C/T]GTTTCCCCAGGGGGA | 330171 |
rs29584128 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kctd10 | Mm_Celera | 5:114374303 | CTGTGACCCACAGCC[A/G]GTTTACAATGCGGCC | 330171 |
rs29584443 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd10 | Mm_Celera | 5:114372115 | GGGAGCGGTGGGAGC[C/T]GAGGGAGCTTAGTGC | 330171 |
rs29629260 | snp | A/G | 0.48 | 0.0979796 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114379687 | ACTGATCTTGTGAGT[A/G]AGTGGCAGACAAAGA | 330171 |
rs29629501 | snp | C/T | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114375353 | TCTAGGAGAGGAACA[C/T]ATCCCTCTCAGCTCA | 330171 |
rs29632964 | snp | C/T | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114371330 | GCAATGCATGCCAGC[C/T]TTCACAGTCACTCAG | 330171 |
rs29633446 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Kctd10 | Mm_Celera | 5:114366845 | GCGTGTGGAGCCTAC[A/G]TCAGCGGAAGACAGA | 330171 |
rs29679929 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd10 | Mm_Celera | 5:114372010 | CCAGTGCGGGCAGAA[A/G]GCTAGACCACTGTGA | 330171 |
rs29731149 | snp | C/T | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114369296 | CCAGACATCCCCGCC[C/T]GGCCCGGCCCCCAAG | 330171 |
rs29778625 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114372651 | CCTGAGAGGATTGCA[C/T]GTAATAAAATGAGCG | 330171 |
rs29781721 | snp | A/G | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Kctd10, Ube3b | Mm_Celera | 5:114382387 | CCAGAGTGCTCATGG[A/G]ACAGTGCTGTGAGGT | 330171 |
rs33037430 | snp | A/G | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114372325 | TGAGCCGGGACTATT[A/G]ACTCATGATGTCATA | 330171 |
rs33080989 | snp | C/T | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Kctd10 | Mm_Celera | 5:114368261 | AATGCCCCCCCACCA[C/T]CCCGCCCAGCTGAGG | 330171 |
rs33090304 | snp | A/T | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114377599 | GGCAAGATCCCCGAA[A/T]GTATCCCAGCTATCA | 330171 |
rs33092781 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Kctd10 | Mm_Celera | 5:114367128 | AGCCCTCTCTGCTTG[C/T]CCAGTGTCGGTAGGA | 330171 |
rs33103527 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Kctd10, Ube3b | Mm_Celera | 5:114381332 | TCCTCCTCTGTAAAT[A/G]GAGTAATTAGATTGT | 330171 |
rs33121388 | snp | C/G | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114369130 | ACTCTGTCTGCCCCC[C/G]CAGAAGGACACACCA | 330171 |
rs33162195 | snp | A/G | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114373234 | TCTCTGAGCACCAGC[A/G]CTGACCACGTGGCTT | 330171 |
rs33166572 | snp | A/G | 0.375 | 0.216506 | utr-variant-3-prime | Kctd10, Myo1h | Mm_Celera | 5:114364093 | GCGAGATCAGGCACC[A/G]TGGAATGTTCACTAG | 330171 |
rs33175513 | snp | C/T | 0.493827 | 0.0552116 | utr-variant-3-prime | Kctd10 | Mm_Celera | 5:114365151 | GGCTCTGTACAAAAC[C/T]GCACACAGAGCAGAC | 330171 |
rs33205196 | snp | G/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114371423 | CCTGTCCAGTGTACT[G/T]TAAGGCAGATTCCCA | 330171 |
rs33239520 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Kctd10 | Mm_Celera | 5:114366744 | GCTCCAGCTCACAAC[C/T]CCAGGGAATCCGATG | 330171 |
rs33349139 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Kctd10 | Mm_Celera | 5:114369525 | AAAACTCGTGACCCT[C/T]CTGCCTCTGCCTTCT | 330171 |
rs33362340 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Kctd10 | Mm_Celera | 5:114370922 | GTTCCCCTAAGCTCT[A/G]TCCCAAGGTCTCCTC | 330171 |
rs33362460 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kctd10 | GRCm38.p3 | 5:114374339 | CCACCTATGAAGAAT[C/T]TCCCCAAGAAGCTTG | 330171 |
rs33382851 | snp | A/G | 0.375 | 0.216506 | downstream-variant-500B, utr-variant-3-prime | Kctd10, Myo1h | Mm_Celera | 5:114363407 | AGGCTCCCGGATCCC[A/G]GGGGGAGTCGGGGCC | 330171 |
rs33395055 | snp | C/G | 0.5 | 0 | intron-variant | Kctd10 | Mm_Celera | 5:114369302 | ATCCCCGCCCGGCCC[C/G]GCCCCCAAGCAGGAG | 330171 |
rs33424951 | snp | C/G | 0.188366 | 0.242283 | intron-variant, utr-variant-3-prime | Kctd10 | Mm_Celera | 5:114368452 | GGCACACTGGCTGCC[C/G]GAAGGCTGTGGGCAC | 330171 |
rs33446158 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114371486 | GGCCATTGCTAAATG[C/T]CCCTTAGGTCACAGA | 330171 |
rs33492547 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB, intron-variant | Kctd10, Ube3b | Mm_Celera | 5:114381691 | TAAGAGCTGTTGTCT[C/T]ATCTTAGGCTTTTAA | 330171 |
rs33506282 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Kctd10 | Mm_Celera | 5:114367891 | ACAGAGACCCAAGAG[A/T]CAGGGCCACTGATGT | 330171 |
rs33530488 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114379714 | AAGAAGACCTGGGTT[A/G]ATAGTCCACCCGCCC | 330171 |
rs33540303 | snp | A/C | 0.444444 | 0.157135 | intron-variant, downstream-variant-500B | Kctd10 | Mm_Celera | 5:114367938 | TTTCATGTTCACGGC[A/C]GCATCTATAACAGAC | 330171 |
rs33580392 | snp | A/G | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114375115 | ACATCTCTTCCTGCC[A/G]GAGAGAAGACAGGGT | 330171 |
rs33594875 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Kctd10 | Mm_Celera | 5:114370502 | TGTAAACGAAAAGGC[A/G]GCCTGGGACACTGGG | 330171 |
rs33595101 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114370883 | TGAACCCCAGCTCTG[C/T]CACCTGCCTGCTCCA | 330171 |
rs33601179 | snp | A/T | 0.444444 | 0.157135 | intron-variant, upstream-variant-2KB | Kctd10, Ube3b | Mm_Celera | 5:114378609 | GGAAAGCCAGACAAA[A/T]AAGACAGGGGAAAAC | 330171 |
rs33627315 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114371464 | TGTGACAACCAAAAC[C/T]ACCTTTGGCCATTGC | 330171 |
rs33680478 | snp | C/T | 0.188366 | 0.242283 | intron-variant | Kctd10 | Mm_Celera | 5:114366693 | AAGGTTGGGCAAGCA[C/T]GCCTAGAGAGAGGTG | 330171 |
rs33723339 | snp | C/T | 0.32 | 0.24 | intron-variant | Kctd10 | Mm_Celera | 5:114374070 | TCTGGCTTTGGGTGA[C/T]GGGCCCACCCACTCA | 330171 |
rs33730599 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Kctd10 | Mm_Celera | 5:114374022 | GTTGCTGAAGGACTC[C/T]TGTACCAAAGCAGTG | 330171 |
rs33741372 | snp | C/T | 0.5 | 0 | intron-variant, utr-variant-3-prime | Kctd10 | Mm_Celera | 5:114368636 | CACTCCTTATATCCC[C/T]GCCACAGACAAGCCC | 330171 |
rs33743983 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Kctd10 | Mm_Celera | 5:114377760 | TGGAGACTGTCTCCA[A/G]CTATGAATAACTGAA | 330171 |
rs33748945 | snp | C/T | 0.375 | 0.216506 | intron-variant | Kctd10 | Mm_Celera | 5:114369496 | AGTGTTGCTAGGTAG[C/T]CTGGGCTGCCCTCAA | 330171 |
rs33754510 | snp | A/G | 0.375 | 0.216506 | intron-variant, utr-variant-3-prime | Kctd10 | Mm_Celera | 5:114368637 | ACTCCTTATATCCCT[A/G]CCACAGACAAGCCCC | 330171 |
rs45670320 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114370253 | GCAGCAGGAAAACCA[A/G]GTCACAGGGCACTTG | 330171 |
rs45747195 | snp | A/C | 0.336735 | 0.234472 | utr-variant-3-prime, downstream-variant-500B | Kctd10, Myo1h | Mm_Celera | 5:114364893 | AGTGTCTGCGGTCAC[A/C]CCAGTTCCTAACCAA | 330171 |
rs45801075 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime, downstream-variant-500B | Kctd10, Myo1h | Mm_Celera | 5:114364563 | GTCGCTAAATAGAAA[C/T]TTTAAAACCTGTCAG | 330171 |
rs45832897 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Kctd10 | Mm_Celera | 5:114372315 | GGGAAACGCCTGAGC[C/T]GGGACTATTGACTCA | 330171 |
rs45874441 | snp | A/G | 0.32 | 0.24 | intron-variant | Kctd10 | Mm_Celera | 5:114373644 | GAAGCCCTAATGTGG[A/G]TCCCTCTCTCCACCG | 330171 |
rs45897270 | snp | C/T | 0.32 | 0.24 | intron-variant | Kctd10 | Mm_Celera | 5:114365922 | GCACATGGCCACTAC[C/T]TCACACTACATCTCA | 330171 |
rs45936192 | snp | C/G/T | | | intron-variant | Kctd10 | GRCm38.p3 | 5:114371576 | GAAGTGCAGGCAGAG[C/G/T]CCTGTCTAGCAAGTG | 330171 |
rs46040486 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Kctd10 | Mm_Celera | 5:114375635 | CCTGAGTGCAGGCAA[C/T]GGCCGGATGAGGAAG | 330171 |
rs46114469 | snp | C/T | 0.32 | 0.24 | intron-variant | Kctd10 | Mm_Celera | 5:114375950 | GGCACTGCAAGGCCT[C/T]GGACACCATCACAGA | 330171 |
rs46224047 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114370404 | CCTGCCTGTGTCCTG[C/T]CTTCAACGCACCACC | 330171 |
rs46231031 | snp | C/T | | | intron-variant | Kctd10 | Mm_Celera | 5:114375377 | CAGCTCACCCCAATC[C/T]ACACCTCATCTCACG | 330171 |
rs46413654 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114366197 | CAGTGAAGGGAGAGA[A/G]CTTGCAAAGCTATTC | 330171 |
rs46462165 | snp | A/G | 0.32 | 0.24 | upstream-variant-2KB, intron-variant | Kctd10, Ube3b | Mm_Celera | 5:114381438 | CGTATTTTGACTTAA[A/G]CCTAGCTAGCCTCAC | 330171 |
rs46536903 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Kctd10, Myo1h | Mm_Celera | 5:114363930 | ATTGTGAGCCCTTAG[C/T]GTGCAGTAAAAGTTC | 330171 |
rs46668276 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Kctd10 | Mm_Celera | 5:114377473 | AAGATAGAACAGTTC[C/G]GTCTCATTGAAAGAA | 330171 |
rs46672377 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Kctd10 | Mm_Celera | 5:114369804 | TCTCAGGGAACAGAC[C/T]GAGCACCTGAGGCAG | 330171 |
rs46711413 | snp | A/G | 0.142012 | 0.225474 | intron-variant, downstream-variant-500B | Kctd10 | Mm_Celera | 5:114368311 | ACAGTGGCGGGCCGG[A/G]CCGCTGCTGTCCGCT | 330171 |
rs46723636 | snp | A/T | 0.124444 | 0.216185 | utr-variant-3-prime, downstream-variant-500B | Kctd10, Myo1h | Mm_Celera | 5:114364553 | TGTACAAACCGTCGC[A/T]AAATAGAAATTTTAA | 330171 |
rs46762327 | snp | A/C/G/T | 0.32 | 0.24 | intron-variant | Kctd10 | GRCm38.p3 | 5:114372959 | GGAGCCAAGGTCCCG[A/C/G/T]GCCAGAATTTCATTC | 330171 |
rs46905927 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Kctd10 | GRCm38.p3 | 5:114370137 | CAGCTCCTCGATCTC[C/T]CGGCGGCTCTCAGGC | 330171 |
rs47159842 | snp | A/C | 0.32 | 0.24 | intron-variant | Kctd10 | Mm_Celera | 5:114369684 | CCACATATGCAGCAT[A/C]TCCTTGGGCTGAAAT | 330171 |
rs47322774 | snp | A/G | | | intron-variant | Kctd10 | Mm_Celera | 5:114375334 | GGCTGCTGGACGGTG[A/G]CCTTCTAGGAGAGGA | 330171 |
rs47337836 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114366772 | ATGCACCAGCACTCA[C/T]GTGCACAAACCCCCT | 330171 |
rs47495268 | snp | A/G | | | intron-variant | Kctd10 | Mm_Celera | 5:114375385 | CCCAATCTACACCTC[A/G]TCTCACGGGCCAACA | 330171 |
rs47529873 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB, intron-variant | Kctd10, Ube3b | Mm_Celera | 5:114382227 | CTTAGGTGTGATGAG[C/T]GTTTCCAAGTGCCAG | 330171 |
rs47582405 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Kctd10 | Mm_Celera | 5:114368215 | AGTCACTCAACCGCA[C/T]GACATGAAGCTGGAT | 330171 |
rs47597210 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Kctd10 | Mm_Celera | 5:114369648 | ACCATGAAGGCCCCC[A/G]AAAGACAATGGCTCC | 330171 |
rs47848897 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114366031 | CTTGACTACACTTCG[A/G]CCTCCAGCGGATTCA | 330171 |
rs48035876 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114367093 | ATCCGGCCAGATTGC[C/T]CGGAGACAGCTGGGA | 330171 |
rs48311911 | snp | A/C | 0.32 | 0.24 | intron-variant | Kctd10 | Mm_Celera | 5:114370497 | GTTTCTGTAAACGAA[A/C]AGGCGGCCTGGGACA | 330171 |
rs48368284 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Kctd10 | Mm_Celera | 5:114369347 | TGCAGTGAGAGACAG[A/G]GCAGAGCGTAGATGT | 330171 |
rs48538262 | snp | C/T | 0.277778 | 0.248452 | upstream-variant-2KB, intron-variant | Kctd10, Ube3b | Mm_Celera | 5:114382454 | CTGACTTGAAGGCCT[C/T]TCTAGTTACAGTCTT | 330171 |
rs48653584 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114369169 | GCCTGGGAGGACACT[C/T]AAAACTCAGCCCTCG | 330171 |
rs48670298 | snp | C/T | 0.32 | 0.24 | intron-variant | Kctd10 | Mm_Celera | 5:114365886 | GCCCCACAAAATACA[C/T]GGTGGGAACGTTAGC | 330171 |
rs48867308 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Kctd10 | Mm_Celera | 5:114371781 | AAACAGAGCCCACGA[A/G]GAAGCAGGACCCAGA | 330171 |
rs49051858 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Kctd10 | Mm_Celera | 5:114369750 | TTCTCAAATGACGCC[C/T]GAACAAACCAATACA | 330171 |