SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs8251140 | snp | C/G | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7947077 | GGGGTGGAGGGTGAA[C/G]CCAGCCAGCCATGTC | 15185 |
rs8251141 | snp | A/G | 0.444444 | 0.157135 | splice-acceptor-variant, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7947032 | TCTGTCTGATTGGCA[A/G]AAGCGTGGNGNAAAN | 15185 |
rs8251142 | snp | G/T | 0.5 | 0 | synonymous-codon, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7947023 | TTGGCANAAGCGTGG[G/T]GNAAANAAGTGTGCT | 15185 |
rs8251143 | snp | A/G | 0.244898 | 0.249948 | missense, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7947021 | GGCANAAGCGTGGNG[A/G]AAANAAGTGTGCTGT | 15185 |
rs8251144 | snp | A/G | 0.244898 | 0.249948 | synonymous-codon, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7947017 | NAAGCGTGGNGNAAA[A/G]AAGTGTGCTGTACCC | 15185 |
rs8251145 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, upstream-variant-2KB | Hdac6, LOC105243649 | GRCm38.p3 | X:7946986 | CACTCCAGCCCCAAT[C/T]TAGCGGNGGTAAANA | 15185 |
rs33373975 | snp | C/T | 0.132653 | 0.220748 | upstream-variant-2KB, nc-transcript-variant | Hdac6, LOC105243649 | Mm_Celera | X:7948294 | GCTATGGCTGCCAGT[C/T]TCAAGTCCAGGCTAG | 15185 |
rs33373977 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB, nc-transcript-variant | Hdac6, LOC105243649 | Mm_Celera | X:7948364 | TGCAGTGATTCGAGA[A/G]CAAATCAAAGAAGCT | 15185 |
rs33373980 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB, intron-variant | Hdac6, LOC105243649 | Mm_Celera | X:7948883 | GTGGTGGACCGAGGA[A/G]GGAAAATTGTCCCTG | 15185 |
rs33373983 | snp | C/T | 0.152778 | 0.230321 | upstream-variant-2KB, intron-variant | Hdac6, LOC105243649 | Mm_Celera | X:7949223 | TAGGATGGTGATGCC[C/T]GCCAGCCGAACAATA | 15185 |
rs33377294 | snp | A/T | 0.375 | 0.216506 | missense | Hdac6 | Mm_Celera | X:7931528 | GGGACTGCTGAGCCG[A/T]GACTCCCTGCAGAGG | 15185 |
rs33377297 | snp | C/T | 0.260355 | 0.249785 | synonymous-codon | Hdac6 | Mm_Celera | X:7931574 | CTGCTTGTTTGTATG[C/T]GAGGCTGGAGGCGTT | 15185 |
rs33377299 | snp | A/T | 0.21875 | 0.248039 | missense | Hdac6 | Mm_Celera | X:7931588 | GCGAGGCTGGAGGCG[A/T]TGGCTCAGTTTCTCC | 15185 |
rs33377301 | snp | A/G/T | 0.444444 | 0.157135 | synonymous-codon | Hdac6 | Mm_Celera | X:7931616 | TCCCAAAGCCTCCAC[A/G/T]GAGGTGGTCTGGTTA | 15185 |
rs33377303 | snp | C/T | 0.375 | 0.216506 | missense | Hdac6 | Mm_Celera | X:7931809 | AGAGTAGACTCTTTC[C/T]CAGGTAGTGCTGCTA | 15185 |
rs33378306 | snp | A/G | 0.260355 | 0.249785 | synonymous-codon | Hdac6 | Mm_Celera | X:7931838 | TATGGTCTTCCTCAC[A/G]CTTTCTTCAGGAACC | 15185 |
rs33378308 | snp | C/T | 0.260355 | 0.249785 | synonymous-codon | Hdac6 | Mm_Celera | X:7931865 | AACCTTTCCTTTCGG[C/T]GTGGTCATTTCCTTA | 15185 |
rs33378311 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Hdac6 | Mm_Celera | X:7931979 | AACAATGGGAAAGAC[A/G]TGTAAGTGTGGCTGC | 15185 |
rs33378313 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac6 | Mm_Celera | X:7932268 | GAATGGGTTCCATGA[C/T]GAGTCATCAGGGAAT | 15185 |
rs33379286 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Hdac6 | Mm_Celera | X:7932449 | TGTAAATTGGTGGCT[A/G]TCACGTGCAAGGTAA | 15185 |
rs33379289 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Hdac6 | Mm_Celera | X:7932665 | AATCTGACCCATACC[A/G]AAGCTCAAGGCAGAT | 15185 |
rs33379291 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Hdac6 | Mm_Celera | X:7932939 | TGATCCTAGGCCCTG[A/C]GTGCCATACAAGTTC | 15185 |
rs33380164 | snp | A/T | 0.165289 | 0.235211 | intron-variant | Hdac6 | Mm_Celera | X:7933020 | AACCCTTAGCCTTCC[A/T]TAAGCAATCCTGGGC | 15185 |
rs33380166 | snp | A/C | 0.32 | 0.24 | intron-variant | Hdac6 | Mm_Celera | X:7933022 | CCCTTAGCCTTCCAT[A/C]AGCAATCCTGGGCAA | 15185 |
rs33380167 | snp | G/T | 0.297521 | 0.245442 | intron-variant | Hdac6 | Mm_Celera | X:7933235 | ATGTCTTGTAAGCCC[G/T]TGAGTTTCTCTGTGA | 15185 |
rs33380170 | snp | C/G | 0.32 | 0.24 | intron-variant | Hdac6 | Mm_Celera | X:7933373 | GACAGGGCATTTTTA[C/G]AGACCAGGAATGCCT | 15185 |
rs33380172 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hdac6 | GRCm38.p3 | X:7934339 | GCAGTAAGGAGAGAA[A/G]AGAAGATGCCCTGAG | 15185 |
rs33381224 | snp | A/C | 0.48 | 0.0979796 | intron-variant | Hdac6 | Mm_Celera | X:7935192 | CCAACCAGACAGGTT[A/C]ATATTGATAGGGCTG | 15185 |
rs33381227 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Hdac6 | Mm_Celera | X:7935225 | AATCCCACCACTTAC[A/G]CTTGGGTTTCTCATG | 15185 |
rs33381230 | snp | C/G | 0.244898 | 0.249948 | intron-variant | Hdac6 | Mm_Celera | X:7935340 | ACACATACACATAAA[C/G]GGTAGCCTCTGTCGC | 15185 |
rs33381232 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac6 | Mm_Celera | X:7935563 | TTCATATATAGACAC[A/G]TGGACCCAGTTAGAC | 15185 |
rs33381368 | snp | A/G | 0.197531 | 0.244432 | utr-variant-3-prime, upstream-variant-2KB | Hdac6, Eras | Mm_Celera | X:7930266 | GGGTAGAACAGAGGT[A/G]TTCCTCGAGCAGGCA | 15185 |
rs33381371 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac6 | Mm_Celera | X:7930610 | AGAGAGGCTGTCACC[A/G]TGGTAGCAGCAGCTT | 15185 |
rs33381436 | snp | A/C | 0.32 | 0.24 | synonymous-codon | Hdac6 | Mm_Celera | X:7937689 | GATGAGACAGCGAGC[A/C]GCAAGGCCCACCTCC | 15185 |
rs33381439 | snp | A/G | 0.444444 | 0.157135 | synonymous-codon | Hdac6 | Mm_Celera | X:7937854 | ACACTTGTCCCAGAG[A/G]TTGCAGTGACTCATC | 15185 |
rs33381442 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Hdac6 | Mm_Celera | X:7938080 | CTCTTGAGACAAAAC[A/G]TGGCCTGGACATAAA | 15185 |
rs33382065 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hdac6 | Mm_Celera | X:7935655 | AGACAGCAGCATTTA[A/G]TGACATACACTATCA | 15185 |
rs33382067 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac6 | Mm_Celera | X:7935684 | CACACTTATCACACA[C/T]AGAAAGGAGATGACA | 15185 |
rs33382068 | snp | A/G | 0.489796 | 0.070696 | intron-variant | Hdac6 | Mm_Celera | X:7935708 | GATGACAGCCACTAT[A/G]TAACATTACATAGAC | 15185 |
rs33382071 | snp | A/G | 0.42 | 0.183303 | intron-variant | Hdac6 | Mm_Celera | X:7935764 | GCTTCTATTCTACAC[A/G]ATTCCACAACAGTAT | 15185 |
rs33382234 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Hdac6 | Mm_Celera | X:7931452 | ACCTCCTTCCCAGAT[C/G]TGGTGGACTTTACCT | 15185 |
rs33382237 | snp | C/T | 0.42 | 0.183303 | missense | Hdac6 | Mm_Celera | X:7931492 | TGCTTAGCTCCAAAG[C/T]GCTGAGAACCCCAAG | 15185 |
rs33382395 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac6 | Mm_Celera | X:7938557 | AGAGTAACAATGTTC[A/G]GGTGCATACTATGTC | 15185 |
rs33382398 | snp | C/G | 0.375 | 0.216506 | intron-variant | Hdac6 | Mm_Celera | X:7938590 | GCAACAAGAAATGTC[C/G]ATTCACGGAAAGTGA | 15185 |
rs33382400 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Hdac6 | Mm_Celera | X:7938673 | TTCATGAACTGGTAA[A/G]GCTGAGCCAAGAACA | 15185 |
rs33382403 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac6 | Mm_Celera | X:7939107 | TAGCCCCAAGGAACT[C/T]CTTACATTCATGAAA | 15185 |
rs33383004 | snp | A/G | 0.32 | 0.24 | synonymous-codon | Hdac6 | Mm_Celera | X:7936258 | GCAGGGACACGTATA[A/G]TACACTGCCAGGGAG | 15185 |
rs33383007 | snp | C/T | 0.32 | 0.24 | intron-variant | Hdac6 | Mm_Celera | X:7936579 | GAGTTAATGAGAAAG[C/T]ACTGCTATTATTCTA | 15185 |
rs33383010 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Hdac6 | Mm_Celera | X:7936638 | AACTATGGACCTGAA[A/C]AAGTAATTAAGGCTA | 15185 |
rs33383013 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac6 | Mm_Celera | X:7936798 | TGGGGCTTTTGTAGT[C/T]AAGTGCTGCCCAGTG | 15185 |
rs33383355 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon | Hdac6 | Mm_Celera | X:7939763 | GATCTGCGAGACCTC[A/C]GAGGCAACTGGCAGC | 15185 |
rs33383358 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac6 | Mm_Celera | X:7939841 | CTGCAGACACAAAAG[C/T]GGGATGCAATTGTCA | 15185 |
rs33383360 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Hdac6 | Mm_Celera | X:7940143 | AAGAGTCAAATGTAC[A/G]ACTCTCAACCTACAG | 15185 |
rs33383362 | snp | A/C | 0.375 | 0.216506 | intron-variant | Hdac6 | Mm_Celera | X:7940442 | TCAATCTGTGCTCAT[A/C]TGTTAAGATACTTCC | 15185 |
rs33383786 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hdac6 | Mm_Celera | X:7937136 | TCATCTTTCCCAGGC[C/T]TCCCTTTCTCCTGTC | 15185 |
rs33383789 | snp | C/T | 0.375 | 0.216506 | intron-variant | Hdac6 | Mm_Celera | X:7937163 | TGTCCGCCATCCACT[C/T]GGCCATCCACTCCGT | 15185 |
rs33383792 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac6 | Mm_Celera | X:7937289 | AAACTTCACTAGCAC[A/G]CAGAGAAGACGCACC | 15185 |
rs33384345 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Hdac6 | Mm_Celera | X:7941692 | GGGAAGGCCACAGTT[C/T]CCGCTTTAGAGTGAA | 15185 |
rs33384348 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Hdac6 | Mm_Celera | X:7941732 | CAGTAGACAACAAGG[A/G]AAAGCATCCACTTCC | 15185 |
rs33384350 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Hdac6 | Mm_Celera | X:7941962 | GGCTAAGTGAAACAC[A/T]GAGGAACAACCTAGA | 15185 |
rs33384353 | snp | A/C | 0.197531 | 0.244432 | intron-variant | Hdac6 | Mm_Celera | X:7942295 | AAGCCAACACTCTCT[A/C]AACCAAGGAGATTTA | 15185 |
rs33384595 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Hdac6 | Mm_Celera | X:7937310 | AAGACGCACCTCTCC[C/T]GAGAGCACAGCTTCC | 15185 |
rs33384596 | snp | A/G | 0.375 | 0.216506 | synonymous-codon | Hdac6 | Mm_Celera | X:7937677 | CCGAGCAGGTAGGAT[A/G]AGACAGCGAGCCGCA | 15185 |
rs33385286 | snp | A/C | 0.297521 | 0.245442 | intron-variant | Hdac6 | Mm_Celera | X:7942588 | CCACTGGTGTATGCT[A/C]TCAAAGCCTGAAGAG | 15185 |
rs33385289 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Hdac6 | Mm_Celera | X:7942745 | TTTTTTTTTTAAATG[C/T]ACGGTACGGAAAGGA | 15185 |
rs33385292 | snp | A/T | 0.244898 | 0.249948 | intron-variant | Hdac6 | Mm_Celera | X:7942920 | TGAGATGTCACGCAC[A/T]GTTCGCTGCATCTGA | 15185 |
rs33386155 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac6 | Mm_Celera | X:7943555 | CCTAACTATTTAGCT[C/T]TTCATTCCCACAGTG | 15185 |
rs33386157 | snp | A/C | 0.336735 | 0.234472 | intron-variant | Hdac6 | Mm_Celera | X:7943598 | ATACGGTAGACACCC[A/C]AGACTTGCTGCCACA | 15185 |
rs33386160 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Hdac6 | Mm_Celera | X:7943798 | CGCAGACAGACCTCG[A/C]ATTAAGTCGGGCCTC | 15185 |
rs33386163 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac6 | Mm_Celera | X:7944027 | TTGCCTCTTGGAACT[C/T]AGCTCAGATATTCTC | 15185 |
rs33386956 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Hdac6 | Mm_Celera | X:7944260 | GATTTCTTTTTCTTT[C/T]GGGATTGGCTTTTTC | 15185 |
rs33386959 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Hdac6 | Mm_Celera | X:7944830 | AATCACGCATACACA[C/T]AGATAGGCAAAAGTG | 15185 |
rs33386961 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Hdac6 | Mm_Celera | X:7944964 | ATACTTGTTTTCTCC[A/G]CTACCATTCACGCTG | 15185 |
rs33387844 | snp | C/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7946191 | TAGTTAGGCGAGGAC[C/T]CTCTAACAATCTAAC | 15185 |
rs33387847 | snp | G/T | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7946340 | CTACAGAGACCTGGA[G/T]TGCCCAGTCATTTGG | 15185 |
rs33387850 | snp | A/G | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7946439 | AGAAGGGACTTTTCT[A/G]TTGCTCACATCTATC | 15185 |
rs33387853 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7946464 | TCTATCACTAAGTCT[C/T]GGCACACAGGAGACT | 15185 |
rs33388646 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Hdac6, LOC105243649 | GRCm38.p3 | X:7946893 | CAAGTTGCAGCCAGG[C/T]CTCTCTCACCAGCCC | 15185 |
rs33388648 | snp | A/G | 0.336735 | 0.234472 | utr-variant-5-prime, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7947738 | CAGGGCCGAACCAGC[A/G]CCTTCCACTCGCGCA | 15185 |
rs33388651 | snp | C/G | 0.244898 | 0.249948 | upstream-variant-2KB, nc-transcript-variant | Hdac6, LOC105243649 | Mm_Celera | X:7947991 | ACGCCGCCAAATTCC[C/G]GGCGACCTGTGTGGC | 15185 |
rs33388653 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, nc-transcript-variant | Hdac6, LOC105243649 | Mm_Celera | X:7948023 | CCGGGCACCTGATCC[C/T]TTCTTTTCCATTGGG | 15185 |
rs45648723 | snp | A/T | | | downstream-variant-500B, upstream-variant-2KB | Hdac6, Eras | Mm_Celera | X:7930070 | TTCTTCCCTCAGTTG[A/T]GCTGGCTAGGAATGA | 15185 |
rs45736551 | snp | C/T | | | intron-variant | Hdac6 | Mm_Celera | X:7940529 | GGCGTAAGCCCTTTT[C/T]TACATCTGCCTCCTC | 15185 |
rs49661252 | snp | G/T | | | downstream-variant-500B, upstream-variant-2KB | Hdac6, Eras | Mm_Celera | X:7929988 | ATTTTAGTTAAATTG[G/T]TTTTTTTGGGGGGGG | 15185 |
rs51586781 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hdac6, LOC105243649 | Mm_Celera | X:7949420 | TCATGTCTCAGCTTT[C/T]TGAGCAGCTGGGCAA | 15185 |
rs211775796 | snp | C/T | | | intron-variant | Hdac6 | Mm_Celera | X:7938123 | CACAGCCCTTCCCAC[C/T]GAGGCATCCCGGGAA | 15185 |
rs211896619 | snp | C/G | | | intron-variant | Hdac6 | Mm_Celera | X:7943614 | AGACTTGCTGCCACA[C/G]CCTGACCCCACAGTT | 15185 |
rs211908251 | snp | C/T | | | intron-variant | Hdac6 | Mm_Celera | X:7945157 | aagccaaacttctca[C/T]cacaccgagaagggc | 15185 |
rs211953433 | in-del | -/AA | | | downstream-variant-500B, upstream-variant-2KB | Hdac6, Eras | Mm_Celera | X:7930100 | CGGGTTTTTCAAAAT[-/AA]AAAAAAAAAAAGCAC | 15185 |
rs211959351 | in-del | -/GGGT | | | intron-variant | Hdac6 | Mm_Celera | X:7938833 | TTACACCCTCTTCTG[-/GGGT]GTCTGAAGATAGCTA | 15185 |
rs212102690 | snp | C/T | | | intron-variant | Hdac6 | Mm_Celera | X:7940390 | TCTTAACCACTGAGC[C/T]ATCTCTCCAGCCCTA | 15185 |
rs212387581 | snp | C/T | | | intron-variant | Hdac6 | Mm_Celera | X:7933029 | CCTTCCATAAGCAAT[C/T]CTGGGCAAACTGTAA | 15185 |
rs212424483 | snp | A/G | | | synonymous-codon | Hdac6 | Mm_Celera | X:7932217 | CATAGACTCAGAGAT[A/G]GATGCCAAATTGTAT | 15185 |
rs212464282 | snp | C/T | | | intron-variant | Hdac6 | Mm_Celera | X:7941273 | CTTGTCACAGGAATC[C/T]ATCTGCCTTGGCCTC | 15185 |
rs212648482 | snp | A/G | | | intron-variant | Hdac6 | Mm_Celera | X:7939082 | GCTCTCAACAACTGA[A/G]CCACCCCTGTAGCCC | 15185 |
rs212688810 | snp | C/T | | | upstream-variant-2KB, intron-variant | Hdac6, LOC105243649 | Mm_Celera | X:7949230 | GTGATGCCCGCCAGC[C/T]GAACAATAGAGACGG | 15185 |
rs213288984 | in-del | -/T | | | intron-variant | Hdac6 | Mm_Celera | X:7944418 | TGTGTTTTTTTTTTG[-/T]TTTTGTTTTTTGTTT | 15185 |
rs213644737 | snp | C/T | | | intron-variant, upstream-variant-2KB | Hdac6, LOC105243649 | Mm_Celera | X:7945954 | CCTTAAGAGCAAAGT[C/T]CTGGCCTTGAAGTAT | 15185 |
rs213738095 | in-del | -/G | | | intron-variant | Hdac6 | Mm_Celera | X:7943762 | AAGATAGAGGAAAGA[-/G]TTTTACAGCCCTGGT | 15185 |
rs213838833 | snp | A/C | | | intron-variant | Hdac6 | Mm_Celera | X:7942595 | TGTATGCTATCAAAG[A/C]CTGAAGAGAACCAAA | 15185 |