SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6326131 | snp | C/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146785860 | TCCAGAAGCAAAGCA[C/T]gggctggagagacgg | 22217 |
rs6326213 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146785916 | ccttttaggggacct[A/G]gtgccatttntggca | 22217 |
rs6326231 | snp | C/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146785926 | gacctngtgccattt[C/G]tggcacccatatggc | 22217 |
rs6326706 | snp | A/C | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146786006 | ccctcttctagcccg[A/C]gggggtactgcaagc | 22217 |
rs6341252 | snp | C/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146786336 | GACCAACACTGTACA[C/T]ATTAACCCAACTTCT | 22217 |
rs6341832 | snp | A/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146786471 | aaaaagtgcttgcct[A/T]gcantcgcaacgncc | 22217 |
rs6341838 | snp | C/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146786475 | agtgcttgcctngca[C/T]tcgcaacgncctggg | 22217 |
rs6341860 | snp | C/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146786484 | ctngcantcgcaacg[C/T]cctgggttcaatccc | 22217 |
rs6342338 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | GRCm38.p3 | 5:146786556 | actcaagaggaagac[A/G]caataggatcanagc | 22217 |
rs6379538 | snp | A/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146788861 | GACTTGAGGGGAGGA[A/T]ATGTGTATTCACTGT | 22217 |
rs6379622 | snp | A/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146788916 | CTAACACTAAAAAGA[A/T]GCTAGGAAAATCAAA | 22217 |
rs6380099 | snp | C/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146788951 | ACTGTGAGCTGCCAA[C/T]GTGAGCACAGACAGC | 22217 |
rs6380128 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Usp12 | GRCm38.p3 | 5:146788969 | GAGCACAGACAGCAT[C/G]ATCACATCGGTTACA | 22217 |
rs6380657 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146789047 | CAATGCTCACCAAAA[A/G]CTGTCTAACTTgggc | 22217 |
rs6382659 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146782860 | TCCAAACTCAAATAC[A/G]GTTTTACTCTTCAAT | 22217 |
rs6383144 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146782927 | GTTATATAGACCCTA[A/G]AAGTGACTGAAAGTT | 22217 |
rs6383321 | snp | A/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783009 | CCAACATGAGAAGCT[A/T]TCCATCACCCACAAG | 22217 |
rs6383894 | snp | C/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783101 | AGGCTCGCCTCGAAG[C/T]GTGGCCGGCCACNTG | 22217 |
rs6383917 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783114 | AGNGTGGCCGGCCAC[A/G]TGTACCNNGTGAACA | 22217 |
rs6383936 | snp | A/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783121 | CCGGCCACNTGTACC[A/T]NGTGAACANGAAGCA | 22217 |
rs6383937 | snp | A/C | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783122 | CGGCCACNTGTACCN[A/C]GTGAACANGAAGCAC | 22217 |
rs6384362 | snp | G/T | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783130 | TGTACCNNGTGAACA[G/T]GAAGCACTCTCGGCC | 22217 |
rs6384388 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783152 | CTCTCGGCCTTATCC[A/G]GCTCACACACACACA | 22217 |
rs6398037 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146783362 | CCGTTGTAAAATTAG[A/G]GAGACATGAGGAGCC | 22217 |
rs29513783 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp12 | Mm_Celera | 5:146766780 | TTAAATGTTTTGGAA[C/T]TTTATTTTTATTTTA | 22217 |
rs29522400 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Usp12, LOC102638199 | Mm_Celera | 5:146795810 | GTCCAAAGCATTCAA[A/G]AGACCGAGAATTTGA | 22217 |
rs29526356 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp12 | Mm_Celera | 5:146793620 | CCCAGAACACAAAAA[A/C]GGAGATGAAGCAGGT | 22217 |
rs29526456 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Usp12 | GRCm38.p3 | 5:146748905 | GGTCAGGCTAGAAGA[C/G]AGACTGCTTACTTAC | 22217 |
rs29528619 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp12 | GRCm38.p3 | 5:146791422 | ACTAAGTACAGAACT[C/T]AGCAGTTCATGAACC | 22217 |
rs29560331 | snp | A/G | 0.375 | 0.216506 | synonymous-codon, intron-variant | Usp12 | GRCm38.p3 | 5:146763250 | GGGCGGGATCACGCC[A/G]ACCTTCTTCTTCTGG | 22217 |
rs29564483 | snp | C/G | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146748497 | CAACAATATTAAAGA[C/G]GAGTTCAGAGTGTTT | 22217 |
rs29566833 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146773681 | AATGGTAGAATACAT[A/G]CCACATCATGTAAGA | 22217 |
rs29591610 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146757463 | TAAAGGTGAGATAGC[A/G]GAAGTCAATGACCTT | 22217 |
rs29626886 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp12 | GRCm38.p3 | 5:146771537 | GCAGAGACTGTGGCC[A/G]TCACTCCGATAATAA | 22217 |
rs29630670 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146759314 | CATGGGGCTCCTGTC[C/T]CAATGACACCTACAG | 22217 |
rs29631919 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Usp12 | GRCm38.p3 | 5:146737482 | AGCATGATTCCTGAG[C/T]AAAAAATTCAACTAC | 22217 |
rs29632933 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp12 | Mm_Celera | 5:146782398 | TGAGATGGAGAAATG[C/T]CCGACAACTGACGTG | 22217 |
rs29636687 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146750721 | CCACAGATGTAGCGT[A/G]TGGTTCCGGCCTGGC | 22217 |
rs29674098 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146763421 | ATTCCCAAACTACGA[A/G]AGGAAAGAATGACGC | 22217 |
rs29676297 | snp | G/T | 0.5 | 0 | intron-variant | Usp12 | GRCm38.p3 | 5:146787241 | AGCCAGGGGTACAAA[G/T]AGAGACCCTGTCTCA | 22217 |
rs29683522 | snp | A/C | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146767777 | GACGGGAACAGGACT[A/C]GAAACTGACCTCTGA | 22217 |
rs29683885 | snp | C/T | 0.5 | 0 | intron-variant | Usp12 | GRCm38.p3 | 5:146792318 | GAAGAGAGTTACTCG[C/T]TGGACAGTTCACATT | 22217 |
rs29684711 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146754267 | GCGTGACGCAGACTG[C/T]AGCGAGCATCCTGGC | 22217 |
rs29686258 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Usp12 | GRCm38.p3 | 5:146793154 | AGATGGATACTTGAC[A/G/T]AAACTGAGTGAATGA | 22217 |
rs29687391 | snp | G/T | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146764437 | TTAGCCATCATCATT[G/T]CCATCTTCAAAGTAG | 22217 |
rs29728281 | snp | G/T | 0.5 | 0 | intron-variant | Usp12 | GRCm38.p3 | 5:146789953 | GCAACCCCCTCTGAC[G/T]TTGTATAATGGATTG | 22217 |
rs29728451 | snp | A/G | 0.5 | 0 | intron-variant | Usp12 | Mm_Celera | 5:146741200 | TGGGGGACAAGTGGA[A/G]TGTGGCCAGTGACAA | 22217 |
rs29729765 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146766126 | TATACCAAGAGCCAA[A/G]CTTTCCCCAGATCCT | 22217 |
rs29778154 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp12 | Mm_Celera | 5:146768223 | CAAGTGGCAAGATTT[A/G]TATAATAATGAGGCA | 22217 |
rs29818429 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Usp12 | Mm_Celera | 5:146785027 | AGGTCAGGGAACATG[A/G]GAAACCTCTAAGGTA | 22217 |
rs32358854 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146756355 | CACAAGGAAACAGAA[A/G]TCTGGAGATATCCTA | 22217 |
rs32358855 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146756452 | AGCTCTCCGTGAACA[C/T]GGGGCATGGCTACAT | 22217 |
rs32358856 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146756499 | AGGAAGGAAGCGGAG[C/T]ATGTACGGCTCCATC | 22217 |
rs32358857 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146756728 | CTTCCCATCCGGCTG[C/T]TTCTTAAGCCCTTTC | 22217 |
rs32358858 | snp | A/T | | | intron-variant | Usp12 | Mm_Celera | 5:146756905 | CAACTTACCCAGTGT[A/T]AGGTGGCTCCCCTGA | 22217 |
rs32358859 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146757152 | CTGGATTCCAGGCCC[C/T]GAAAGCCCCGTGAGA | 22217 |
rs32358860 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146757167 | CGAAAGCCCCGTGAG[A/G]CGTATAAGAGCCCAA | 22217 |
rs32358861 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146757609 | TGACTTTCCAGCCTG[C/T]AGCTGCCACTTCTAA | 22217 |
rs32358862 | snp | A/C | | | intron-variant | Usp12 | Mm_Celera | 5:146758088 | TGAGGAAGTGAAGGG[A/C]GGCAGGAAGTCTTTC | 22217 |
rs32358863 | snp | A/C | | | intron-variant | Usp12 | Mm_Celera | 5:146758119 | TAAGAATAGCTGGGA[A/C]CCTAGTTACCAGCTT | 22217 |
rs32359024 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146783476 | GTCCGGAAGCTCTCC[C/T]TGGACCGGCCTGCCC | 22217 |
rs32359025 | snp | A/G/T | | | intron-variant | Usp12 | GRCm38.p3 | 5:146783947 | TTTGTGTAATGCACC[A/G/T]TCAAAAGCCACAAAC | 22217 |
rs32359026 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146784015 | TCCTCCCTTAACATG[A/G]ATTCAGTCTGTATCA | 22217 |
rs32359027 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146784067 | TAGCTCTCTCTTGAC[A/G]GTGATTTGTTCTAAA | 22217 |
rs32359028 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146784461 | CGGTCTGAAGAGGCA[C/T]AGCTGTGTCTCCAGC | 22217 |
rs32359029 | snp | C/T | | | intron-variant | Usp12 | GRCm38.p3 | 5:146784505 | CATGAGATTTCAAAG[C/T]GAAAACTGCAGCCAG | 22217 |
rs32359030 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146784538 | CCCGCTGTATACGTA[C/T]GACCCACTCCATCCA | 22217 |
rs32359031 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146784555 | ACCCACTCCATCCAC[C/T]TCATGACCCCTCAAG | 22217 |
rs32359032 | snp | A/C | | | intron-variant | Usp12 | Mm_Celera | 5:146784609 | AGATTCTGGAAGCCG[A/C]CTCCCTCAGGAGAGA | 22217 |
rs32359033 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146784674 | CAAGGAACCTCATTT[A/G]TAATACTTGTAAAAG | 22217 |
rs32359299 | snp | A/G | | | downstream-variant-500B | Usp12 | Mm_Celera | 5:146734351 | GGAAGTGGGATAGAC[A/G]GACAGACAGACAGAC | 22217 |
rs32359300 | snp | A/G | | | downstream-variant-500B | Usp12 | Mm_Celera | 5:146734568 | GCCCCAATTGCCGAG[A/G]AACTGAGGCTCCTAG | 22217 |
rs32359301 | snp | C/T | 0.375 | 0.216506 | downstream-variant-500B | Usp12 | GRCm38.p3 | 5:146734619 | CTTTCCTTGTTAGAA[C/T]TTATTCACCTTGGGA | 22217 |
rs32359302 | snp | C/T | | | utr-variant-3-prime | Usp12 | Mm_Celera | 5:146735607 | TTCAAAATGTCTTCC[C/T]CAGATCCATCTGCAC | 22217 |
rs32359303 | snp | C/T | | | utr-variant-3-prime | Usp12 | Mm_Celera | 5:146735715 | GCAGGCCTGCTCGCC[C/T]GGAGGTTGGCTCCCA | 22217 |
rs32359744 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146758157 | TACCTCATGGCAGTG[A/G]GCAGCACACACTGGA | 22217 |
rs32359745 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146758176 | GCACACACTGGATCA[A/G]CGCCACCATCTCTAA | 22217 |
rs32359746 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146758782 | ATGACTTTGTCATCA[C/T]TCCACTCTTCACATT | 22217 |
rs32359747 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146758912 | GAATGAATGAATGAA[C/T]GAACAAATAAATGAA | 22217 |
rs32359748 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146759044 | ATGCCATATCTAGTA[C/T]ACAGGCTAAGGTTTA | 22217 |
rs32359749 | snp | A/T | | | intron-variant | Usp12 | Mm_Celera | 5:146759091 | TCAAAGCCACTGATA[A/T]GGCTCAAGGCCACCT | 22217 |
rs32359750 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146759154 | CACTGACAGTCACCT[C/T]ACTCACCTGTGTGGC | 22217 |
rs32359751 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp12 | GRCm38.p3 | 5:146759463 | GCCTCTAATCTCACC[C/T]GATCAAAAAACCTAG | 22217 |
rs32359752 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146760567 | GCCTGTGCACATACC[A/G]GGAGATAAAACCTAG | 22217 |
rs32359753 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146760656 | ATTAACAAATGGAAG[C/T]GGCAACGAGGGTGAC | 22217 |
rs32359774 | snp | A/G/T | | | intron-variant | Usp12 | GRCm38.p3 | 5:146784723 | ATCCTACATGAGCCC[A/G/T]TGCTACAGTCCTCAG | 22217 |
rs32359775 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146785193 | TGGCTAGAACTGTGC[C/T]GTTTATAGGAGCCAC | 22217 |
rs32359776 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp12 | GRCm38.p3 | 5:146785636 | CTGGACATACTCTGA[C/T]GGTCTAGTAGTTCAC | 22217 |
rs32359777 | snp | A/T | | | intron-variant | Usp12 | Mm_Celera | 5:146785699 | CACACCTGATTATGT[A/T]GGAAGTGTTTGACTT | 22217 |
rs32359778 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146785744 | CATACCATAAAGATA[C/T]GAAGCACGTCACAAA | 22217 |
rs32359779 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146785763 | GCACGTCACAAACTT[A/G]TACCGGATCTTTGCT | 22217 |
rs32359780 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146785781 | CCGGATCTTTGCTCA[A/G]GGATGGTGCCAATCT | 22217 |
rs32359781 | snp | C/T | | | intron-variant | Usp12 | Mm_Celera | 5:146787323 | AACCAAGCTAAAATA[C/T]CTTACTAGAAATGTT | 22217 |
rs32359782 | snp | A/G | | | intron-variant | Usp12 | Mm_Celera | 5:146787372 | CCTCAGCCAGCCAGC[A/G]CACATCACACTGTAC | 22217 |
rs32359783 | snp | C/G | | | intron-variant | Usp12 | Mm_Celera | 5:146787702 | TGAGTGGCCTACATT[C/G]ACATCTAGGACTTAA | 22217 |
rs32360274 | snp | A/G | | | utr-variant-3-prime | Usp12 | GRCm38.p3 | 5:146736623 | AGAGACCGGAAGAAC[A/G]CGCCATGCCACCGCC | 22217 |
rs32360275 | snp | A/G | | | utr-variant-3-prime | Usp12 | Mm_Celera | 5:146736636 | ACACGCCATGCCACC[A/G]CCGCAGCTGTGCACG | 22217 |
rs32360276 | snp | C/T | | | utr-variant-3-prime | Usp12 | Mm_Celera | 5:146736638 | ACGCCATGCCACCGC[C/T]GCAGCTGTGCACGGT | 22217 |
rs32360277 | snp | C/G | 0.444444 | 0.157135 | utr-variant-3-prime | Usp12 | Mm_Celera | 5:146737045 | AAGATCATTACAAAG[C/G]CAGTCTTTCCCCTTG | 22217 |
rs32360278 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Usp12 | GRCm38.p3 | 5:146737288 | TGTACGCATCCCGCA[C/T]GCTGGCACACAGTGC | 22217 |