SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6321802 | snp | C/T | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112042912 | ACTGGAAGACAAGTG[C/T]ACTTGCTTCTGCCCA | 74996 |
rs6322231 | snp | A/G | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112042929 | CTTGCTTCTGCCCAC[A/G]ATGGCTTCCTGAAGG | 74996 |
rs6322290 | snp | C/T | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112042954 | TGAAGGACACCTCCC[C/T]GATTCGGGACTGGTG | 74996 |
rs6335369 | snp | C/G | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112043018 | TGGCAGTTGATGGTG[C/G]TGTGAGGTCAGTTTT | 74996 |
rs6335947 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112043113 | TCCAGAGCTGTTCTC[A/G]GAGTTTTTTAGTNTG | 74996 |
rs6335972 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Usp47 | Mm_Celera | 7:112043126 | TCNGAGTTTTTTAGT[C/T]TGTACACTCACATAG | 74996 |
rs6336086 | snp | A/G | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112043198 | CCTTTTTTGGTTTAT[A/G]TAAAATTTTACTGAT | 74996 |
rs6366360 | snp | C/T | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112057296 | gtgtttgataatgcg[C/T]atctgtataccatat | 74996 |
rs6368109 | snp | A/C | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112057623 | GAAATAAAAACAAGT[A/C]CAGAGATGTCTTTTG | 74996 |
rs6368573 | snp | C/T | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112057673 | GCATGGTTTTTGAAT[C/T]TTTCTTTTTAAAAAT | 74996 |
rs6368586 | snp | C/T | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112057690 | TTCTTTTTAAAAATT[C/T]GAAAAAGATTTTAAA | 74996 |
rs6369141 | snp | A/G | 0.5 | 0 | intron-variant | Usp47 | Mm_Celera | 7:112057787 | GACCTATAGTATTAT[A/G]TTTGTTATATTTTAT | 74996 |
rs6382927 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Usp47 | Mm_Celera | 7:112058042 | AATGATTGCTTAAAA[C/T]GTCAATTTCCAGGTT | 74996 |
rs6382993 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Usp47 | Mm_Celera | 7:112058099 | CTCTGAGTCAGGACA[A/G]AAAATTGTTCATCTT | 74996 |
rs6383044 | snp | A/G | 0.304688 | 0.243945 | intron-variant | Usp47 | Mm_Celera | 7:112058131 | TTTTAAATAAGTACT[A/G]TGAAGATTGTTCTGA | 74996 |
rs6384733 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Usp47 | Mm_Celera | 7:112058359 | AAACATGCCATTTGT[C/T]ACATTATAAAATTAA | 74996 |
rs13462454 | snp | A/G | 0.231111 | 0.249285 | synonymous-codon | Usp47 | Mm_Celera | 7:112091464 | CTGCTACAATGACCT[A/G]CGCCTTCTCAGCATG | 74996 |
rs31199755 | snp | A/C | 0.375 | 0.216506 | utr-variant-3-prime | Usp47 | Mm_Celera | 7:112110864 | CCAGCTGCAGCTTCG[A/C]TGTCTGCCAAGGTTC | 74996 |
rs31564396 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Usp47 | Mm_Celera | 7:112065874 | TGTAAGTACACTGTA[G/T]TTGTCTTCAGACACA | 74996 |
rs32182719 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Usp47 | Mm_Celera | 7:112103078 | ACCCTGTGGTGTGTC[A/G]ACAGGCTGCTGGAGT | 74996 |
rs32266066 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112031241 | AATGGCTAGTTTCTG[A/C]GCCTCCTCTTTTTAA | 74996 |
rs32266069 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112032362 | AAAATGTAAATAAGC[A/G]TGTATCCGAGGTGCC | 74996 |
rs32266072 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112032924 | GATGGAGGGAGAAGG[G/T]TCAAACATTTTCAGA | 74996 |
rs32266073 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp47 | Mm_Celera | 7:112033099 | ATTTTTAGTCAGCAA[A/G]CTTAGAACTCTACAG | 74996 |
rs32266245 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Usp47 | Mm_Celera | 7:112037910 | AAATTCATATGTGTT[A/G]AAATATTTGCTAGTG | 74996 |
rs32266248 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112039114 | ATAAGCCAGTAGTTT[A/T]ACATCACTTCTCTGT | 74996 |
rs32266251 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112039356 | ATGTGCTTGCCGGAT[A/T]AGTTATTAGCCGTTG | 74996 |
rs32266253 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112039695 | AAGGACTCTAGCCAG[A/G]TGCTCTGACTTCAGC | 74996 |
rs32266916 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112033391 | TTCTTGATTCTTCTG[C/T]CTCAATCTGATTGTT | 74996 |
rs32266918 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112033519 | GATAGGACAGAATTT[C/T]TAGTTCAAAATACTA | 74996 |
rs32266920 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112033533 | TTTAGTTCAAAATAC[C/T]AATGGTAAAATACTT | 74996 |
rs32266923 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112033607 | TGCTAGTGTGGGAAA[A/G]AGTTACTCAGTAAAC | 74996 |
rs32267056 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Usp47 | Mm_Celera | 7:112040544 | AACAGGAATAGTAAA[C/G]ACTTACTGTTTCACC | 74996 |
rs32267058 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112040556 | AAACACTTACTGTTT[C/T]ACCTCCTAAAAATAA | 74996 |
rs32267061 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112041059 | CAGGCATAAATATTA[A/C]AAGCATACTTTATCC | 74996 |
rs32267063 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112041073 | ACAAGCATACTTTAT[C/T]CAAGTCAGCCTGTAT | 74996 |
rs32267746 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112033656 | CCTTTGTTATCACCT[C/T]CATCCTTACTTCTTG | 74996 |
rs32267749 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp47 | Mm_Celera | 7:112033667 | ACCTCCATCCTTACT[C/T]CTTGGAACAGCATCC | 74996 |
rs32267752 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112034325 | TTAAACAACCACATA[A/G]ATTGCTCACTTGTAA | 74996 |
rs32268056 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112042279 | ATCTCAGTGGTGAGT[A/G]CTTGGACTTCTTCCA | 74996 |
rs32268059 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112042409 | ATTTCCAGTCCTGTA[A/G]ATGGGTCTGTTGTTT | 74996 |
rs32268061 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112042520 | CAGCAGACTTGACTG[C/T]GACAGCGCAAGTGGA | 74996 |
rs32268063 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112042547 | TGGAGTTTCAGGTTC[A/G]GGCCCTGCCAGGCGC | 74996 |
rs32268535 | snp | C/G | 0.391111 | 0.206368 | intron-variant | Usp47 | Mm_Celera | 7:112034475 | GTTTAGCTGATTGCT[C/G]TAAGACCTATAGCCT | 74996 |
rs32268538 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112034753 | TTAAGAGCTTTTAGG[A/G]AAAATATTTTTAAAA | 74996 |
rs32268541 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112034993 | TAAGATATATTCTAG[A/C]GCAGCAGTTCTCAAC | 74996 |
rs32269136 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112042697 | CTTGGATTTACTGAA[A/G]ATGCACTTCTTGGTG | 74996 |
rs32269138 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112042807 | TGGGGAAACTTTGTT[A/G]TGACTTTCAGCTGTT | 74996 |
rs32269334 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Usp47 | Mm_Celera | 7:112035328 | CGGTACTAAAAATCT[A/G]TCTATGGATGAACCC | 74996 |
rs32269337 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112035488 | AGAGAGAATTTTAGC[A/G]TCGGGCAGTGGTGGT | 74996 |
rs32269340 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112035833 | CATTCAGTTCAGATA[G/T]GGAGCTTAAAACCTG | 74996 |
rs32269343 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112036092 | GAGCAACAGTTAAAA[C/G]AGAAAAGGCTGTAAT | 74996 |
rs32269935 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112043575 | TACACATTTTCCTAG[A/G]TAAGTTTTATGGATT | 74996 |
rs32269937 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Usp47 | Mm_Celera | 7:112044059 | TTATTTGGGAGCTGC[A/G]GCAGGCTTAGAAAAG | 74996 |
rs32269939 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112044164 | TTGGATTGCATTTGG[A/G]ACGCTTGCAGTTTTT | 74996 |
rs32269940 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112044226 | GTGTGTCTGCTATAA[A/C]CCAGAGCTTCTATAG | 74996 |
rs32269943 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Usp47 | Mm_Celera | 7:112044271 | ATGGCCAGACAGCAG[C/G]GGGACATATGAATAT | 74996 |
rs32269996 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112036192 | TCTGGCAGGCTGAGT[A/C]CAAACGTTCCAGAGG | 74996 |
rs32269999 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112036353 | GAAAGAGTTTTTTCC[A/C]AGATATTTTATGTCC | 74996 |
rs32270001 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112036397 | AATTTGCATATAAGT[A/G]AAAATGAGAGGAATA | 74996 |
rs32270784 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112036637 | GCCTTTAGAAAATGC[C/T]ACCAGTTACAGTCTG | 74996 |
rs32270787 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112036654 | CCAGTTACAGTCTGA[C/T]CGTGGGTGTGTCCAG | 74996 |
rs32270790 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112036793 | ACACAAACCAGGATG[A/G]TGTAGTTTTTCCTTA | 74996 |
rs32270793 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112036828 | TCTGTGTTGGCACAT[C/G]CTCATGAATGCTATG | 74996 |
rs32271055 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112044282 | GCAGCGGGACATATG[A/G]ATATTTTTAATGATG | 74996 |
rs32271058 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Usp47 | Mm_Celera | 7:112044445 | ATCGATAATTTTACA[C/T]ATTTCAGCATTTCTT | 74996 |
rs32271061 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112044495 | GTTCTTGTTGGTTAC[A/G]GCTCAGGTAGCAGGC | 74996 |
rs32271063 | snp | A/T | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112044542 | CTGTAAATATTCTTT[A/T]CCAACTTTCCAACTT | 74996 |
rs32271626 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112036841 | ATGCTCATGAATGCT[A/G]TGCAGCTGTTGTTTC | 74996 |
rs32271628 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Usp47 | Mm_Celera | 7:112037451 | TATCTACTTCTTTAC[G/T]CACTAGAGAGTGACC | 74996 |
rs32271631 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112037511 | GACATCCCTCCAGGA[A/G]TGTTTTTATTTGGGG | 74996 |
rs32271793 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112028731 | CTTCATGTAGGAAAC[A/G]TCTCTTATACGGTTA | 74996 |
rs32271905 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112044576 | GCCCTTTCTGTTTTG[C/T]TAACTCTACATGTCT | 74996 |
rs32271908 | snp | A/T | 0.375 | 0.216506 | intron-variant | Usp47 | Mm_Celera | 7:112045219 | TATAGATATTTTTTT[A/T]TTTTGTATTTCATTC | 74996 |
rs32271911 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112045368 | TAGAAGATTTTTGGA[A/G]ACGAAGACACTAGGT | 74996 |
rs32272394 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112046302 | GAATAGAAAAGGTTT[G/T]GGTAGAACATATATT | 74996 |
rs32272397 | snp | A/T | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112046354 | TTTAGAATTGCCCTT[A/T]AAAAAAAACTCTTGT | 74996 |
rs32272400 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112047186 | TTAACAAGTGAGTAA[A/G]GGAGAACTGAAAGAA | 74996 |
rs32272403 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Usp47 | Mm_Celera | 7:112047249 | TAATATTAGTACAGA[C/T]ATATTTATTTTCTGC | 74996 |
rs32272405 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Usp47 | Mm_Celera | 7:112089063 | AAAAGTGAAAGAAAA[C/T]CAGACAAACTATACT | 74996 |
rs32272408 | snp | A/T | 0.124444 | 0.216185 | missense | Usp47 | Mm_Celera | 7:112089566 | GATCTGAAAGCAGAG[A/T]CTGTCGCTGCTCCTG | 74996 |
rs32272411 | snp | C/T | 0.244898 | 0.249948 | synonymous-codon | Usp47 | Mm_Celera | 7:112089622 | GACAGTTACAGAGTT[C/T]AAACAGCTGATCTCA | 74996 |
rs32272444 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112066462 | GTCAGAAGAGCCCTG[A/G]CTGGCTGTGAGAAGT | 74996 |
rs32272446 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112067342 | ATGATTGTGTGTTCT[G/T]TTTACTAAGCCACAG | 74996 |
rs32272448 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112068037 | ATTTCTGATCACCTC[A/G]TAAGATTTTTAGCAT | 74996 |
rs32272451 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112068384 | TGATAATATTTCAAG[A/G]TCCATGGAGATTCTG | 74996 |
rs32272504 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Usp47 | Mm_Celera | 7:112037586 | TTAAGACTTTACTAC[C/G]TAAGGAAACTTTGAT | 74996 |
rs32272506 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp47 | Mm_Celera | 7:112037695 | AATACTGATAAGCTG[C/T]CTATGATCTTATATA | 74996 |
rs32272508 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112037707 | CTGTCTATGATCTTA[C/T]ATACAGCTTGTCATG | 74996 |
rs32272511 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112037806 | TATTTTAGTAGTTTG[C/T]GGTTATGAAAAGGAA | 74996 |
rs32272513 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112037869 | TCTAATACAAAAGAC[A/G]TGAGAGATACTAGTT | 74996 |
rs32272695 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp47 | Mm_Celera | 7:112028757 | GGTTACCACTTTGTA[A/G]CTCTGCCTCTGTAAT | 74996 |
rs32272698 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112029015 | ATTCACAGTTCTCAG[G/T]TTTTTTTCTAAATTA | 74996 |
rs32272700 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp47 | Mm_Celera | 7:112029032 | TTTTTTCTAAATTAT[C/T]AGTTTAGCAGATGGT | 74996 |
rs32272702 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112029460 | AGTGTACACATTTTG[C/T]TCTTACAGTCACACC | 74996 |
rs32272794 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112045445 | AGGACAGGAGATGAG[A/G]GGTAGCAGGAAGATT | 74996 |
rs32272797 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Usp47 | Mm_Celera | 7:112045485 | AGAGGGAAGAGGTGA[A/G]CTGTTCTGATTATCT | 74996 |
rs32272799 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112045512 | ATCTTCAGTTATGTA[A/G]CTACTGGTCCCCACT | 74996 |
rs32272801 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Usp47 | Mm_Celera | 7:112045843 | GGCCCTTCCATATAT[C/G]TAAAGAGTATGGCAC | 74996 |
rs32273036 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp47 | Mm_Celera | 7:112053994 | CTGCATGGAGGCTGA[C/T]TAAATGTGCAGTATT | 74996 |