SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3684266 | snp | C/T | 0.489796 | 0.070696 | upstream-variant-2KB | Asb14 | GRCm38.p3 | 14:26894051 | GCAGCTCAGGGAATA[C/T]GTAGGTGCGGCTACA | 142687 |
rs3702560 | snp | A/C | 0.5 | 0 | intron-variant | Asb14 | Mm_Celera | 14:26903707 | CTTGGGAGACAGAGG[A/C]AGGCAGATTTCTGAG | 142687 |
rs3702572 | snp | A/T | 0.5 | 0 | intron-variant | Asb14 | Mm_Celera | 14:26903708 | TTGGGAGACAGAGGC[A/T]GGCAGATTTCTGAGT | 142687 |
rs3703136 | snp | A/C | 0.5 | 0 | intron-variant | Asb14 | Mm_Celera | 14:26903797 | CCCTGTCTCGAAAAA[A/C]CAAAACCAAAACAAA | 142687 |
rs3703148 | snp | A/C | 0.5 | 0 | intron-variant | Asb14 | Mm_Celera | 14:26903804 | TCGAAAAACCAAAAC[A/C]AAAACAAAAATAAAG | 142687 |
rs3718616 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Asb14 | GRCm38.p3 | 14:26903980 | CTTTGTATAGTTCTT[G/T]TTGTTTTTATTTGGT | 142687 |
rs6323944 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon | Asb14 | GRCm38.p3 | 14:26903289 | CTTGCTGATCAGCCA[C/T]GGAGCAGATGTCAAT | 142687 |
rs6325095 | snp | G/T | 0.484429 | 0.0868505 | intron-variant | Asb14 | GRCm38.p3 | 14:26903519 | TGGTTGATTACAGGG[G/T]TACTGAGATCCAAGG | 142687 |
rs30151477 | snp | G/T | 0.359862 | 0.224567 | intron-variant | Asb14 | GRCm38.p3 | 14:26912929 | TCCCTCACCTTCAAC[G/T]TTTTCCAGGGCTTTT | 142687 |
rs30153992 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Asb14 | Mm_Celera | 14:26895055 | TATTATTTTACATTA[C/T]TTACATACATCTTTG | 142687 |
rs30171553 | snp | A/T | 0.387812 | 0.208586 | utr-variant-3-prime | Asb14 | GRCm38.p3 | 14:26915228 | AAGGATTTTTTCTTT[A/T]CTTTACTCAGTAAAT | 142687 |
rs30204345 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Asb14 | GRCm38.p3 | 14:26899311 | TGATGAGATCTCATA[A/C]AAACATGGAGAATCA | 142687 |
rs30208284 | snp | A/G | 0.487535 | 0.077957 | synonymous-codon | Asb14 | GRCm38.p3 | 14:26915060 | CCCCGTCTTCATGTC[A/G]TTTCTTCCGCTGCCC | 142687 |
rs30289412 | snp | A/G | 0.415225 | 0.187619 | missense | Asb14 | GRCm38.p3 | 14:26911851 | ACAGACATCGCAGCC[A/G]TCAAGAAGAGCGGGA | 142687 |
rs30399674 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb14 | GRCm38.p3 | 14:26908969 | GAGGCAGAGGCAGGC[A/G]GATTTCTGAGTTCGA | 142687 |
rs30461638 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Asb14 | GRCm38.p3 | 14:26896708 | ACAACCCTCCTCCTC[A/C]TCATCTGCCAGCTCT | 142687 |
rs30479466 | snp | A/G | 0.5 | 0 | intron-variant | Asb14 | GRCm38.p3 | 14:26895315 | TGTGTGTGTGTGCAT[A/G]CATGTGTGTGTACTC | 142687 |
rs30480384 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Asb14 | GRCm38.p3 | 14:26902973 | ATCACTTTGCATACG[C/T]GTCGTTTAAAATGTG | 142687 |
rs30629297 | snp | A/G | 0.387812 | 0.208586 | intron-variant, downstream-variant-500B | Asb14 | GRCm38.p3 | 14:26914790 | ATTTAAGCCAGACTC[A/G]CAATTGATGCAGTTC | 142687 |
rs30706245 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Asb14 | GRCm38.p3 | 14:26896875 | CTCACTGCAAATAGG[A/G]GCTTCTGTAACCAAG | 142687 |
rs30707969 | snp | C/G | 0.456747 | 0.140554 | intron-variant | Asb14 | GRCm38.p3 | 14:26901574 | TCTTATCAGCACAGA[C/G]CTGCCTATTGTCCCA | 142687 |
rs30722111 | snp | C/T | 0.5 | 0 | intron-variant | Asb14 | GRCm38.p3 | 14:26910899 | TCTCCTGTGGGGGGC[C/T]GTGGGGGCGGTAGCT | 142687 |
rs30784854 | snp | A/C | 0.32 | 0.24 | missense | Asb14 | Mm_Celera | 14:26914262 | ATGTTGATCAAGTTC[A/C]AATCTGTTCAAAATT | 142687 |
rs30784855 | snp | A/C | 0.475309 | 0.108333 | intron-variant | Asb14 | GRCm38.p3 | 14:26914097 | AGCTTAGCTCATGGC[A/C]CTTTACACTCTTCTC | 142687 |
rs30784856 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Asb14 | Mm_Celera | 14:26913835 | GTCACAGCTTCATAC[G/T]TAACAGGAGAAACAC | 142687 |
rs30784857 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Asb14 | Mm_Celera | 14:26913800 | CTATGGAACCAGAAG[A/T]AATCTTTCAGGCAGA | 142687 |
rs30784858 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Asb14 | Mm_Celera | 14:26913747 | ACGAACATAAACAAA[C/T]GTTTTTTTTAAAAGG | 142687 |
rs30784859 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Asb14 | Mm_Celera | 14:26913505 | TAATAAAAGCTTTAA[A/T]AAAGTGGCGTCTGGG | 142687 |
rs30784860 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Asb14 | Mm_Celera | 14:26913489 | TAAAAAATGCAAAAA[A/G]TAATAAAAGCTTTAA | 142687 |
rs30784861 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26913265 | CAGTTTGATTAAGTG[A/G]CAGGTTTTATTTTAG | 142687 |
rs30784862 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26913222 | GATCAACATTTGAAA[A/G]CAGGATGATGAATGG | 142687 |
rs30784863 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Asb14 | Mm_Celera | 14:26913045 | TCACTCTCTTATTGT[G/T]GAGATTGGCTCTTTT | 142687 |
rs30785824 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Asb14 | Mm_Celera | 14:26912878 | ACACACACACACACA[C/G]CGCACCTCTTCACTT | 142687 |
rs30785825 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | GRCm38.p3 | 14:26912571 | AGCTCTCAGATCTGA[C/T]CAGCCCATTCCTCTG | 142687 |
rs30785826 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Asb14 | GRCm38.p3 | 14:26912551 | TTTCTTTTATTATGT[C/T]TTCTAGCTCTCAGAT | 142687 |
rs30785827 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | GRCm38.p3 | 14:26912489 | TTTCTTTGTATGATT[C/T]ATTTATCTAAAATGT | 142687 |
rs30785828 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26912395 | CCCTAAGCATTTATT[A/G]TCTTGTAGCGTTAGA | 142687 |
rs30785829 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Asb14 | Mm_Celera | 14:26912279 | TGAGCGATGTTTTGA[C/T]TGTCCTCATGGAGAA | 142687 |
rs30785830 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26911737 | CATAGCACTCAGTGT[A/G]GGGATAACAGTATCA | 142687 |
rs30785831 | snp | G/T | 0.35503 | 0.226867 | intron-variant | Asb14 | Mm_Celera | 14:26911687 | TTAACGAAGGAACTC[G/T]CACTTCCGTTAGGTC | 142687 |
rs30785832 | snp | A/C | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26911607 | GTCTCAGATGACTGC[A/C]GCTAATTCAGAGTTT | 142687 |
rs30785833 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Asb14 | Mm_Celera | 14:26911427 | TCCTAAGAGTTCAGG[C/T]CACCTGCCCATCCAC | 142687 |
rs30786934 | snp | C/T | 0.336735 | 0.234472 | synonymous-codon | Asb14 | Mm_Celera | 14:26911394 | TCTGTTGTTAGAGTA[C/T]GGAGCTGATGCCAAC | 142687 |
rs30786935 | snp | A/G | 0.152778 | 0.230321 | synonymous-codon | Asb14 | Mm_Celera | 14:26911328 | TCAGGCCTCTGACTC[A/G]TCCTCTGTGTTACTT | 142687 |
rs30786936 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Asb14 | Mm_Celera | 14:26911281 | ATCTTTGCCTAATGA[A/G]ACTGCTTCTTTCCAG | 142687 |
rs30786937 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Asb14 | Mm_Celera | 14:26910394 | AGCAACTATATATTT[A/G]CCATGTCTTTTAACA | 142687 |
rs30786938 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb14 | Mm_Celera | 14:26910344 | TATAAGCCACCCTAA[C/T]CCATAACTCACTTGC | 142687 |
rs30786939 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb14 | Mm_Celera | 14:26910287 | CTTGGGACTCCAGTA[A/G]GAATACTTGGTAAAA | 142687 |
rs30786940 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Asb14 | Mm_Celera | 14:26910216 | CCACGGGATAAAAGT[A/C]GTTTCTAAATAACGG | 142687 |
rs30786941 | snp | G/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26909678 | GTGCATTCTAGGAAC[G/T]CGGGTCTTGTGCAGC | 142687 |
rs30786942 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb14 | Mm_Celera | 14:26909640 | CATTGTTAACACTCA[A/G]AAACCATTTATTAGA | 142687 |
rs30786943 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26909224 | TTTAAGTGAGAACCT[A/G]CTTCTGAGGTTGGTG | 142687 |
rs30787834 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Asb14 | Mm_Celera | 14:26909133 | GGAGAGGTGCACACA[C/T]GTCTTAATTGCCTTT | 142687 |
rs30787835 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb14 | Mm_Celera | 14:26908761 | TTGCTACCCTGTGTG[A/G]TCACAGCAGCTATGT | 142687 |
rs30787836 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Asb14 | Mm_Celera | 14:26908696 | GGTTGAGCCCTCATT[C/T]GCCAGTGAGCCAGGA | 142687 |
rs30787837 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Asb14 | Mm_Celera | 14:26908410 | AGACGTCTAAAGTTA[C/T]TGACTAGAAAATCAA | 142687 |
rs30787838 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Asb14 | Mm_Celera | 14:26908378 | TTTAGCATGATGCCT[A/G]ACACATGTGACCTAG | 142687 |
rs30787839 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26908302 | TACAGAGCAGCCCTG[C/T]CCTTTGTACACTTTC | 142687 |
rs30787840 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Asb14 | Mm_Celera | 14:26908279 | ATACCCGACAGAGCC[C/T]CTGATATTACAGAGC | 142687 |
rs30787841 | snp | G/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26908058 | TTGTGGTTTAACTAC[G/T]GTGGACACTTAGCTC | 142687 |
rs30787842 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Asb14 | Mm_Celera | 14:26907988 | CTTCTTCCAATAGGC[C/T]CTCTCTCTTAACTGC | 142687 |
rs30787843 | snp | A/G | 0.35503 | 0.226867 | missense | Asb14 | Mm_Celera | 14:26903272 | GCCTACGACATGGCC[A/G]CCTTGCTGATCAGCC | 142687 |
rs30788615 | snp | A/G | 0.387812 | 0.208586 | utr-variant-3-prime | Asb14 | GRCm38.p3 | 14:26915253 | GTAAATCTCAGTGCA[A/G]ACTACATTGTTTAAA | 142687 |
rs30788994 | snp | C/G | 0.165289 | 0.235211 | intron-variant | Asb14 | Mm_Celera | 14:26903205 | TAATATGATGTTTAA[C/G]CTCATATTGTCATAA | 142687 |
rs30788995 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Asb14 | Mm_Celera | 14:26902903 | AAACGCCCCGTAGAC[A/G]GTTGTACTCACAGCT | 142687 |
rs30788996 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb14 | Mm_Celera | 14:26902891 | TCTCAACCATGTAAA[C/T]GCCCCGTAGACGGTT | 142687 |
rs30788997 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Asb14 | Mm_Celera | 14:26902855 | TTTTCCTGAGAAATA[A/C]AGATGATAACTTGAA | 142687 |
rs30788998 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Asb14 | Mm_Celera | 14:26902502 | GATGCAGCAAGTACC[C/T]GGGCTGCCTCACTGG | 142687 |
rs30788999 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26902337 | TCACATCCACTCCTT[C/T]TCCTTTTTATAATAG | 142687 |
rs30789000 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26902031 | ATATGTAATTCCATC[A/G]TGGTCACCCATCATT | 142687 |
rs30789001 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Asb14 | Mm_Celera | 14:26901718 | GGCAGGTCGACCCTT[A/G]GGTATCTGTATACTA | 142687 |
rs30789002 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26901663 | GAGGAGGCTGTGTTC[A/G]ACTACAGAGCAGTAC | 142687 |
rs30789003 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Asb14 | Mm_Celera | 14:26901257 | TTTGACGAAGAGTCT[C/T]GGTCCCCTCCACGCC | 142687 |
rs30789934 | snp | A/T | 0.336735 | 0.234472 | missense | Asb14 | Mm_Celera | 14:26900972 | ATCTTAGAAATAACC[A/T]TGAACGGTAAACTCC | 142687 |
rs30789935 | snp | A/G | 0.336735 | 0.234472 | missense, utr-variant-5-prime | Asb14 | Mm_Celera | 14:26900895 | ACCATCCAGCCTTTG[A/G]TGAAGCCAATGGGAA | 142687 |
rs30789936 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26900747 | GTTGAGGACGGTGCT[C/T]GGATTCTGCTCTTAC | 142687 |
rs30789937 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb14 | GRCm38.p3 | 14:26900741 | CCTTTGGTTGAGGAC[A/G]GTGCTCGGATTCTGC | 142687 |
rs30789938 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26900679 | GGTCCCCCCTGCACC[C/T]GAGTGGCGAGGAACG | 142687 |
rs30789939 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26900618 | AGTGGTCTTTTCAGC[A/G]TAACTTATCAAAGAA | 142687 |
rs30789940 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb14 | GRCm38.p3 | 14:26900367 | CTGCAGCTGCCTTGG[A/G]TTTCGATCAGAAACA | 142687 |
rs30789941 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Asb14 | GRCm38.p3 | 14:26900180 | TTTCACCCCAAGCGC[A/G]TGTGTGTACGCGGGC | 142687 |
rs30789942 | snp | C/G | 0.5 | 0 | intron-variant | Asb14 | Mm_Celera | 14:26900145 | AATGGGATCTCGCTC[C/G]CTTGCTCGCTCCCTC | 142687 |
rs30789943 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb14 | GRCm38.p3 | 14:26900063 | AAAAGCTGTACCTAA[C/T]AAAGCATGGCAGGTA | 142687 |
rs30790531 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Asb14 | Mm_Celera | 14:26898081 | AAAATTTAAAAACTT[A/G]GAGAGAATTAAGAAT | 142687 |
rs30790784 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Asb14 | GRCm38.p3 | 14:26899980 | CGGGTTTGAGTCAGC[C/T]CTCCAACATTTATTG | 142687 |
rs30790785 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Asb14 | GRCm38.p3 | 14:26899783 | TATACAAAGCTTTAA[G/T]GTTTAGTTATTTTTA | 142687 |
rs30790786 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26899706 | CAGAAATGAGGCAGG[A/G]AAATGAAGCAGCCCT | 142687 |
rs30790787 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Asb14 | GRCm38.p3 | 14:26899518 | CTAACACAGCACCAA[A/G]CCCATTAACACAGTC | 142687 |
rs30790788 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Asb14 | Mm_Celera | 14:26898463 | ACACTTGTTGGTGTT[A/C]GAAATCTAGAGTTGG | 142687 |
rs30790789 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26898414 | AAACTTCAAGATTTA[C/T]ACGATACCTAGGAAA | 142687 |
rs30790790 | snp | A/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26898296 | TTGCTGGAGGGCAAC[A/G]TCTGGGTGAGAAGAC | 142687 |
rs30790791 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Asb14 | GRCm38.p3 | 14:26897867 | CAGCTGAGAGGAGTC[A/G]TGGCCCTCATGTCAC | 142687 |
rs30790792 | snp | C/T | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26897839 | CAGTGAGCACTAAGA[C/T]GTACGTATTCAGCAG | 142687 |
rs30790793 | snp | A/G | 0.32 | 0.24 | synonymous-codon, intron-variant | Asb14 | Mm_Celera | 14:26897775 | TGTTTACAAGCCAGG[A/G]ATAGCTCAGCACACG | 142687 |
rs30791400 | snp | A/T | 0.32 | 0.24 | downstream-variant-500B, utr-variant-3-prime | Asb14 | Mm_Celera | 14:26915266 | CAAACTACATTGTTT[A/T]AAAAGCGTGTTCTGT | 142687 |
rs30791401 | snp | A/G | 0.124444 | 0.216185 | missense | Asb14 | Mm_Celera | 14:26915142 | GAACGTTCTACAGGA[A/G]CATGGTAACTAAGCT | 142687 |
rs30791402 | snp | C/T | 0.32 | 0.24 | synonymous-codon | Asb14 | Mm_Celera | 14:26915048 | ACGTTTGCGCTGCCC[C/T]GTCTTCATGTCGTTT | 142687 |
rs30791403 | snp | C/T | 0.124444 | 0.216185 | missense | Asb14 | Mm_Celera | 14:26915034 | TGTATGGGACGGTTA[C/T]GTTTGCGCTGCCCCG | 142687 |
rs30791724 | snp | A/C | 0.124444 | 0.216185 | missense, intron-variant | Asb14 | Mm_Celera | 14:26897644 | TGGAAAAATATTTTA[A/C]TTCCTTCTGACTTGG | 142687 |
rs30791725 | snp | C/G | 0.32 | 0.24 | intron-variant | Asb14 | Mm_Celera | 14:26897426 | ATTTTCTGGAATAAG[C/G]TTTAAATAAGTGTCT | 142687 |