SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6230765 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Usp30 | Mm_Celera | 5:114108405 | AGATGCGATCCAAGG[C/T]CTCAAGGCCCAGCCT | 100756 |
rs6232039 | snp | A/G | 0.5 | 0 | intron-variant | Usp30 | Mm_Celera | 5:114108681 | cttatatgaggaggt[A/G]tatacttactagagg | 100756 |
rs6284530 | snp | C/T | 0.5 | 0 | intron-variant | Usp30 | GRCm38.p3 | 5:114104940 | gagaggatgccaggt[C/T]cttagctggagtcag | 100756 |
rs13464098 | snp | C/T | 0.32 | 0.24 | synonymous-codon, utr-variant-3-prime | Usp30 | Mm_Celera | 5:114119074 | CTTTGACAGCCTTTC[C/T]CTCAGTATTCCAGCT | 100756 |
rs29720344 | snp | A/G | 0.5 | 0 | intron-variant | Usp30 | GRCm38.p3 | 5:114111776 | GCTGGGCTGCGGGGA[A/G]CGTTGCTGCTGGTCC | 100756 |
rs33077646 | snp | C/G/T | 0.375 | 0.216506 | utr-variant-3-prime | Usp30 | GRCm38.p3 | 5:114122864 | AGCCAGGGGGGGATC[C/G/T]TGACGGCACTGACGT | 100756 |
rs33100848 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp30 | GRCm38.p3 | 5:114107931 | TTGACATTATTTGCA[A/G]CTAAGGAAAGGGGGA | 100756 |
rs33116557 | snp | C/T | 0.444444 | 0.157135 | intron-variant, missense | Usp30 | GRCm38.p3 | 5:114114641 | CCAGCACATCGTGTC[C/T]TTGTGTGCCCATGCC | 100756 |
rs33275407 | snp | A/G | 0.465374 | 0.126941 | utr-variant-3-prime | Usp30 | GRCm38.p3 | 5:114122467 | GCCTTTTGTAATCTC[A/G]AGTTCCCTGTGCCGC | 100756 |
rs33413432 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Usp30 | GRCm38.p3 | 5:114115087 | GTCCCTTTGCTTACA[A/C/T]GGTAAGCGCTCGACC | 100756 |
rs33540302 | snp | C/G | 0.375 | 0.216506 | utr-variant-3-prime | Usp30 | Mm_Celera | 5:114122857 | CATGGACAGCCAGGG[C/G]GGGATCGTGACGGCA | 100756 |
rs33621994 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Usp30 | GRCm38.p3 | 5:114117319 | TGCCTGCCAGCCCTG[A/G]CTCTGTCTTCTGCCA | 100756 |
rs33725621 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Usp30 | GRCm38.p3 | 5:114112739 | AAGGCTCTTCCGTGA[A/G]GATGGAGACTGGCAG | 100756 |
rs36242348 | snp | A/T | 0.426035 | 0.177515 | intron-variant | Usp30 | Mm_Celera | 5:114117312 | CCCTGTCTGCCTGCC[A/T]GCCCTGACTCTGTCT | 100756 |
rs36250557 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114113610 | TGCCATCACTTGGGG[A/G]TGTTTACATTGTTTC | 100756 |
rs36255128 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114110141 | TTCCCATGGCCGCAA[A/G]CCAGGGCTTCACCTG | 100756 |
rs36259285 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114108247 | CAGTGCTTGCCTGGT[A/G]TGCACATGGCCCGGC | 100756 |
rs36277199 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114115648 | GCATCTCCGATTTTT[C/T]CCCAGAATTTATTTA | 100756 |
rs36286121 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114110933 | GCTGCGTGCATCTTG[C/T]CTGCTCTTTTAAAGC | 100756 |
rs36297443 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114112193 | CGTGCCCTGCTGGTC[G/T]TTGGTCCCAGGCAGC | 100756 |
rs36318385 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp30 | Mm_Celera | 5:114116187 | TGGCCACTGTGTCTT[C/T]TAGGAAACACGTGAC | 100756 |
rs36320065 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114109547 | AACCCTGCTACTATA[A/G]CAAGGACAGGAACGT | 100756 |
rs36325935 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp30 | Mm_Celera | 5:114118445 | TGACTGCTGTGCAGT[A/G]TCCCCCATGTCACCG | 100756 |
rs36341425 | snp | A/T | 0.231111 | 0.249285 | downstream-variant-500B, utr-variant-3-prime | Usp30 | Mm_Celera | 5:114123389 | TCACAGTAGGCACCT[A/T]CTTCCCGGAGAAACG | 100756 |
rs36349545 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114111854 | CAGGCTCTCAGTCTC[C/T]TCTTTTCCCTACAGC | 100756 |
rs36359258 | snp | A/C | 0.124444 | 0.216185 | synonymous-codon | Usp30 | Mm_Celera | 5:114121545 | CACATACCTCTTCCG[A/C]TTGATGGCAGTTGTC | 100756 |
rs36417341 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114111990 | CCTTTCAGATAGGAC[A/G]GCACTGTGCCTGTGT | 100756 |
rs36421870 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114106171 | GGGTCGGGAGAGAGC[A/C]CGGTTAGTGTGAGAC | 100756 |
rs36428769 | snp | C/T | 0.142012 | 0.225474 | intron-variant | Usp30 | Mm_Celera | 5:114110691 | AGGGCATGCTTGTTC[C/T]GCTGTGTGCAGGGCC | 100756 |
rs36451352 | snp | C/G | 0.132653 | 0.220748 | intron-variant | Usp30 | Mm_Celera | 5:114110687 | GGCCAGGGCATGCTT[C/G]TTCTGCTGTGTGCAG | 100756 |
rs36512412 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114106967 | AGGAGATACACTGGC[C/T]CAGTCATTCCTGAGT | 100756 |
rs36614716 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Usp30 | Mm_Celera | 5:114112745 | CTTCCGTGAAGATGG[A/T]GACTGGCAGTGCCCG | 100756 |
rs36627469 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Usp30 | Mm_Celera | 5:114115992 | AGGGTGTGCCCTTGT[A/G]AGTGAAAGGCCAACA | 100756 |
rs36721189 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114114180 | TGCAGTCAGAAAGCA[C/T]AGTGCTGCTTGCCTT | 100756 |
rs36753364 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114110774 | ACCAAGGGCAGCAGG[C/T]AGGATGCAGGGGTCA | 100756 |
rs36771289 | snp | C/G | 0.124444 | 0.216185 | synonymous-codon | Usp30 | Mm_Celera | 5:114111203 | CCACTTGTTTGATGT[C/G]CATTCCCTGGAGGTA | 100756 |
rs36771340 | snp | A/T | 0.124444 | 0.216185 | downstream-variant-500B, utr-variant-3-prime | Usp30 | Mm_Celera | 5:114123298 | GTGTCACCCTGACCG[A/T]GCGCTAATGTCCTTC | 100756 |
rs36818925 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114117343 | TCTGCCATCTCGGTC[C/T]TGAACTGTGGCTGCT | 100756 |
rs36855977 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114113286 | CTTCGTGTCTGTCTG[C/T]TCTTGGTGGGCACAG | 100756 |
rs36874730 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114105618 | CAAACATGACTTGCT[C/T]ACTCCGCACTGTGTG | 100756 |
rs36897290 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114110634 | GGAAAGGGTTCTTCA[A/G]CATACTGCTTTGTGT | 100756 |
rs36900068 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114120362 | TGCACTGTCTAAGCA[C/T]TTCCTTCTCCCTCTG | 100756 |
rs36918037 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp30 | Mm_Celera | 5:114120684 | GTACCACAGGCCAGC[C/T]GGTTGACTTGGCAGT | 100756 |
rs36925273 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114113778 | TCCTTTACCTCTCAG[C/T]GAGGGCTTCACCTGC | 100756 |
rs36935031 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Usp30 | Mm_Celera | 5:114122521 | CTCTTCCTGAGCTGT[A/G]TCATCTGCACCTCTG | 100756 |
rs36939891 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114109101 | AAGGATTCCTGACGA[A/G]CAGATGCAGTGCTGA | 100756 |
rs36958030 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114114046 | CAGTAAGTTTTACTT[A/G]TGCTTATTGACAGTC | 100756 |
rs36959157 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114104282 | GCATTCAGTGAGCCC[A/G]TGCAATGTGGTCAGG | 100756 |
rs36961967 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114113532 | CTTTTGGGGTGCATA[A/G]CGCCTCCTGCTGTTT | 100756 |
rs37022848 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114111472 | GCCTGAGCTGCACTC[C/T]TGCTGTTGTGTTTGC | 100756 |
rs37025302 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Usp30 | Mm_Celera | 5:114120557 | TGGCCCCAAAGCCAC[C/T]GAGAACCCAGGGTCT | 100756 |
rs37032703 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114116149 | TGGCAAGGCCACCAG[C/T]GTGAGGCTGAGTAAG | 100756 |
rs37057500 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Usp30 | Mm_Celera | 5:114121665 | ATGGCTGTGGATTTC[C/T]GACGACACCGTCCGC | 100756 |
rs37069907 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114107977 | ACCCAGCCCAGAATG[A/G]CATAGCTCAAGTCTG | 100756 |
rs37092810 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114110985 | GCACGTCTCCTTCAG[C/T]TATTGGGACTCAGAG | 100756 |
rs37098730 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114111663 | ATAGGAGTTGACTGG[A/G]AATAGGGAAAAGATA | 100756 |
rs37163877 | snp | C/T | 0.231111 | 0.249285 | synonymous-codon | Usp30 | Mm_Celera | 5:114121563 | GATGGCAGTTGTCGT[C/T]CACCATGGAGACATG | 100756 |
rs37221503 | snp | A/C | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114103355 | AACTAAAGGAGAGAG[A/C]GTCCAGGAGCGCATG | 100756 |
rs37224307 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp30 | Mm_Celera | 5:114116896 | TATTCAATACAGTAG[A/G]CTCTGGATTCCGAGG | 100756 |
rs37232154 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114109702 | CAAATCTGTCTCTAC[C/T]GTAAAGGTGAAACAG | 100756 |
rs37310740 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114105459 | AGCACACAAGCAGGA[A/G]CAAAGGCTGCAGCAG | 100756 |
rs37315899 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Usp30 | Mm_Celera | 5:114113410 | TGTTAGTCAGTCTTA[A/G]GACATCTGACACATC | 100756 |
rs37316333 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114110624 | CACCCTAACAGGAAA[G/T]GGTTCTTCAACATAC | 100756 |
rs37347976 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114109561 | AACAAGGACAGGAAC[A/G]TACACCTGGGTGACG | 100756 |
rs37432119 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114112012 | TGCCTGTGTCCTGCC[A/G]GTTGGACCTGGTGCA | 100756 |
rs37534471 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp30 | Mm_Celera | 5:114113740 | GTGTCTGACTCCTGA[A/G]GCTAGCCTGCCCTGC | 100756 |
rs37609597 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Usp30 | Mm_Celera | 5:114110673 | CTTGAGGACACTGTG[C/G]CCAGGGCATGCTTGT | 100756 |
rs37762943 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114109628 | GGATCTGACCAGAGA[A/G]GCGCTCGCTCCATAA | 100756 |
rs37843843 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114106180 | GAGAGCACGGTTAGT[A/G]TGAGACGCTCTTTCA | 100756 |
rs37876636 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114111079 | ACCCTAGCCTGGCCT[C/T]GTGAACCTGTCTTCA | 100756 |
rs37894188 | snp | A/G | 0.124444 | 0.216185 | downstream-variant-500B, utr-variant-3-prime | Usp30 | Mm_Celera | 5:114123128 | ACTCCACGACACAGC[A/G]GCCCCACAGACCTGG | 100756 |
rs37917351 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp30 | Mm_Celera | 5:114121395 | TAACAGCCGTAGTTA[A/G]CAATTAGGTGTGCCT | 100756 |
rs37994624 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Usp30 | Mm_Celera | 5:114112728 | GCGGAGGCCTTAAGG[C/T]TCTTCCGTGAAGATG | 100756 |
rs38016098 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114110587 | CAGCCCCACAAAATT[G/T]TTAGACAGGCCAATC | 100756 |
rs38096823 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114106229 | GAGGAGGCTCAAACT[G/T]TCCCCAGACCTCACA | 100756 |
rs38132545 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114115493 | ACCCCCATCAGGCGC[A/G]TGGTTTGCAGAGGCT | 100756 |
rs38374760 | snp | C/T | 0.231111 | 0.249285 | downstream-variant-500B | Alkbh2, Usp30 | Mm_Celera | 5:114123745 | ACAGAGCACTGACTA[C/T]TAAAAATGGCTCTTA | 100756 |
rs38383743 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B, utr-variant-3-prime | Usp30 | Mm_Celera | 5:114123170 | AGATGAACACAAAAG[C/T]CGGCAGTCACTTGTG | 100756 |
rs38563391 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp30 | Mm_Celera | 5:114111933 | GGCGTTTTCCATTGA[C/T]AAAATGCGTATTTAA | 100756 |
rs38570675 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114113805 | CTGCTTCCCTGGGAA[A/T]AACAAGCAAGGCAGA | 100756 |
rs38578473 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114103417 | GCTGCCGCTTTTATC[C/T]GTTTCGTATCTGCGC | 100756 |
rs38766664 | snp | A/C | 0.32 | 0.24 | utr-variant-3-prime | Usp30 | Mm_Celera | 5:114122806 | GTTTCAATAAGCAAA[A/C]GGTACACTGGGCCTC | 100756 |
rs38877903 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114109413 | TGATGGAGACTTTTC[A/G]CTACATGCATGAACA | 100756 |
rs38954085 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114106587 | AGGTTTATCTCACTG[A/G]CTGCACTTGCGAGCT | 100756 |
rs39006395 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp30 | Mm_Celera | 5:114111050 | TCTGTCTGCTGCACG[C/T]GGCCTGGGTTCTGAC | 100756 |
rs39106845 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114112213 | TCCCAGGCAGCAAGC[A/C]CAGCCTCTCATCTGA | 100756 |
rs39141540 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, downstream-variant-500B | Usp30 | Mm_Celera | 5:114119092 | CAGTATTCCAGCTGC[C/T]ACTTGGGTACGTACT | 100756 |
rs39161339 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114116824 | GTTTCACACCAGGCT[A/G]GCTCTCGTGGTTAGT | 100756 |
rs39251865 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114111642 | AACATAATATTTAGG[G/T]CAGTGATAGGAGTTG | 100756 |
rs39305929 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp30 | Mm_Celera | 5:114105862 | AGCAGGTGAGCACTC[C/T]GACAGCAGGAGACCT | 100756 |
rs40061330 | snp | A/T | 0.32 | 0.24 | intron-variant | Usp30 | Mm_Celera | 5:114111730 | CTCATGCAGAATCCA[A/T]CCAGAAGGTGGGTCA | 100756 |
rs47429011 | snp | A/G | | | intron-variant | Usp30 | Mm_Celera | 5:114116305 | CGTGAATGTGCGTGT[A/G]CGTGTACGTGTGCGT | 100756 |
rs51405407 | snp | A/G | | | intron-variant | Usp30 | Mm_Celera | 5:114116311 | TGTGCGTGTGCGTGT[A/G]CGTGTGCGTATGCAT | 100756 |
rs108921208 | snp | C/T | | | upstream-variant-2KB | Usp30 | Mm_Celera | 5:114098895 | AATTAGCATATAAAT[C/T]TATAATCTCATTACT | 100756 |
rs211714730 | snp | A/G | | | intron-variant | Usp30 | Mm_Celera | 5:114101856 | AGGCCTGGTGCCACC[A/G]CTCTGTCACGAATTG | 100756 |
rs211777474 | snp | C/T | | | intron-variant | Usp30 | Mm_Celera | 5:114101072 | GGAAGGAAGGCTTGA[C/T]TGGGCCTTGCGGCCT | 100756 |
rs212105235 | snp | C/T | | | intron-variant | Usp30 | Mm_Celera | 5:114110248 | GCGTGGTGGCGCATG[C/T]CTTTAATCCTAGCAC | 100756 |
rs212379420 | snp | C/T | | | intron-variant | Usp30 | Mm_Celera | 5:114103632 | GTCCTCTTCCTCCCG[C/T]GCCCTCCCTAGGGCT | 100756 |
rs212442045 | snp | C/T | | | intron-variant | Usp30 | Mm_Celera | 5:114102866 | AGCCTGTGCTTTATA[C/T]AGCAAGTACCAGGCC | 100756 |
rs212442349 | snp | A/G | | | intron-variant | Usp30 | Mm_Celera | 5:114110827 | TCCGGAGGCTCAGTC[A/G]GGGATTGATGGCGGT | 100756 |