SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3656972 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:87997232 | TACCCTGGGATTGGA[A/G]TTTCCAGCAGTTATA | 227334 |
rs6302124 | snp | C/T | 0.5 | 0 | intron-variant | Usp40 | Mm_Celera | 1:87991354 | gagcagcaagctgaa[C/T]tgtttctccagtccA | 227334 |
rs6302193 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:87991399 | CAATTGGCTAAAACC[A/G]TAACAGCTAACGGAT | 227334 |
rs13473572 | snp | C/T | 0.304688 | 0.243945 | utr-variant-3-prime, nc-transcript-variant | Usp40 | GRCm38.p3 | 1:87946565 | TTCCTGTGCTTCAGA[C/T]AGAAGCATCCTGTCA | 227334 |
rs30305914 | snp | A/T | 0.489796 | 0.070696 | missense, nc-transcript-variant | Usp40 | Mm_Celera | 1:87986124 | CAGATGGGGCCTGGG[A/T]AAGATGGTTCCTCAG | 227334 |
rs30305915 | snp | G/T | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Usp40 | GRCm38.p3 | 1:87985992 | TGATATCTTTCTCTC[G/T]GATTGGATGGACTTT | 227334 |
rs30305916 | snp | C/T | 0.444444 | 0.157135 | synonymous-codon, nc-transcript-variant | Usp40 | Mm_Celera | 1:87985912 | CATACCTTCAGGGGG[C/T]CTTTGTAACGTGGCT | 227334 |
rs30305917 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Usp40 | Mm_Celera | 1:87985645 | AAAGTGAAGAAAAAT[A/G]TCAGACATCTCCTCA | 227334 |
rs30305918 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:87985143 | TAAAATTTGTGACTG[C/T]ATAGTAGTGCACTTA | 227334 |
rs30305919 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Usp40 | Mm_Celera | 1:87985097 | TAGTCAGCAAACTAG[A/C]AGTGATTTTTCACTT | 227334 |
rs30305920 | snp | A/T | 0.359862 | 0.224567 | intron-variant | Usp40 | Mm_Celera | 1:87983478 | GGCAGTTATATTGGC[A/T]AGTTCTCTGTAAACT | 227334 |
rs30305921 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:87982945 | TGAGAGTTCCATTGA[C/T]CATGGTGTGTCATAC | 227334 |
rs30305922 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:87982900 | AGGCTCTTTTCTGCA[G/T]TTAGCATGTTTCAAT | 227334 |
rs30306313 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88006210 | GTGGTAGTGAGAACT[C/T]GGCATTTAAGTACAA | 227334 |
rs30306974 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:88006098 | CACTGCATTAGAATG[A/G]CACACTAGATGTGGA | 227334 |
rs30306975 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:88006012 | CTGAAGAGTAGAATT[A/G]CTATCAGGAGGCAAC | 227334 |
rs30306976 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88005834 | CTCCACCTCCTACAT[A/G]CTCTCAAGTCTGTTC | 227334 |
rs30306977 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Usp40 | Mm_Celera | 1:88005819 | GGGACCCTTCTCTTG[C/G]TCCACCTCCTACATG | 227334 |
rs30306978 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88005296 | CAGGACCATGCTGAA[A/C]CATGCAGAGTGCACA | 227334 |
rs30306979 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88004949 | TGCAAGTAGTAAGAC[A/T]TGGCAATGACCTTAC | 227334 |
rs30306980 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:88004877 | TGGACCAGGCTGGAC[A/G]TCTTCTACCTTGAGA | 227334 |
rs30306981 | snp | A/G | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Usp40 | GRCm38.p3 | 1:88004256 | TAGTACCTTTGCATC[A/G]GGTTTATCTTTATCC | 227334 |
rs30306982 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88003458 | TATTTATAATAGCAG[A/C]AATAGCAGCATGGTA | 227334 |
rs30306983 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:88003375 | CGGAATGAATGTTCT[A/G]GTCAGCTAGCATGGA | 227334 |
rs30307664 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Usp40 | Mm_Celera | 1:88002769 | TTCCAGCAAACGACA[A/C]AAACGATCACAGACA | 227334 |
rs30307665 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Usp40 | Mm_Celera | 1:88002746 | ATCAATATTAAAATT[A/C]AAATGGGTTCCAGCA | 227334 |
rs30307666 | snp | A/G | 0.46875 | 0.121031 | intron-variant | Usp40 | Mm_Celera | 1:88002689 | TGAAAATTCTATTCA[A/G]TCCAAAAGGTTTTAG | 227334 |
rs30307667 | snp | C/G | 0.46281 | 0.131194 | intron-variant | Usp40 | Mm_Celera | 1:88002657 | ATAGAGGGAGAACTA[C/G]TTAGGATTCGGTCCT | 227334 |
rs30307668 | snp | G/T | 0.32 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:88002583 | GGATTTCAAAAGCTC[G/T]AGACTGGTTTTCTCC | 227334 |
rs30307669 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:88002325 | AAGGCATTCCAAAGT[A/G]CTGAGGCCCTGAGAC | 227334 |
rs30307670 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:88002313 | TACTCACCTGTGAAG[A/G]CATTCCAAAGTACTG | 227334 |
rs30307671 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88001616 | GGATGGACCACAGTC[A/G]TCAGTTGTCTGGATT | 227334 |
rs30307672 | snp | G/T | 0.33241 | 0.236027 | intron-variant | Usp40 | Mm_Celera | 1:88001452 | GGGAATATAGCCCTA[G/T]CACTAGTCCTATATC | 227334 |
rs30307673 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Usp40 | Mm_Celera | 1:88001109 | ACCATGCAGCAGAGG[C/T]TCACTGGGCAGTAAG | 227334 |
rs30308464 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp40 | Mm_Celera | 1:88001009 | AAAAACTAAGAAAAG[C/T]GTTTCAGGACTTTTA | 227334 |
rs30308465 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88000902 | ATCACTAGTTTGAAC[A/G]GGAGAGAAAATCCCA | 227334 |
rs30308466 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Usp40 | Mm_Celera | 1:88000829 | CTGTGTATGACACTG[A/G]TGATCTTGTTCTTGC | 227334 |
rs30308467 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Usp40 | Mm_Celera | 1:88000747 | GGTATAGAAAGAGAG[A/G]CAGCCAGGGGACAAT | 227334 |
rs30308468 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Usp40 | Mm_Celera | 1:88000494 | TCCATTCTAAGTCAC[C/T]GGTCATGTATGAACA | 227334 |
rs30308469 | snp | A/T | 0.495868 | 0.0452663 | intron-variant | Usp40 | Mm_Celera | 1:88000178 | ACCTTTATTTACATT[A/T]CAAAATAGAAATAGG | 227334 |
rs30308470 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Usp40 | Mm_Celera | 1:87999572 | CTGTTTCAAGAATCT[A/G]CAGGCTGTTGAGATG | 227334 |
rs30308471 | snp | C/T | 0.345679 | 0.230967 | intron-variant | Usp40 | Mm_Celera | 1:87999062 | AATTCTCAATCAAGC[C/T]GAATGGGCAATCTGT | 227334 |
rs30308472 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:87999049 | ATGGACACAAACAAA[A/T]TCTCAATCAAGCCGA | 227334 |
rs30308473 | snp | C/G | 0.33241 | 0.236027 | intron-variant | Usp40 | Mm_Celera | 1:87998621 | AATCTTAGTTATTTT[C/G]AAACTAGGCTGACTG | 227334 |
rs30309404 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:87998227 | CCTCATGTTTCCTCA[G/T]GAAATACACTGCAGA | 227334 |
rs30309405 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Usp40 | Mm_Celera | 1:87998155 | TTGGTTTAAAGTACA[C/T]TAGGAAAATAGTTTA | 227334 |
rs30309406 | snp | G/T | 0.33241 | 0.236027 | missense, nc-transcript-variant | Usp40 | GRCm38.p3 | 1:87997904 | TACATGTTGCAGAGT[G/T]CATCTTCTAAACCAG | 227334 |
rs30309407 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:87997774 | TCAGCAGGCACAGCT[C/T]CCTGTCTCCAAGCAC | 227334 |
rs30309408 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Usp40 | Mm_Celera | 1:87997735 | AGCAGTACAGTGTGT[C/T]TTCCTGACTCCACAT | 227334 |
rs30309409 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:87997375 | AGGTATCTTGTTGCT[A/G]TATTAACTCCTTGAT | 227334 |
rs30309410 | snp | A/G | 0.18 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:87996763 | AAGCATATAGCTCTT[A/G]TTCAGTGAAAGAGCA | 227334 |
rs30309411 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Usp40 | Mm_Celera | 1:87996753 | TTCACTTAGCAAGCA[C/T]ATAGCTCTTATTCAG | 227334 |
rs30309412 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Usp40 | Mm_Celera | 1:87996750 | TATTTCACTTAGCAA[A/G]CATATAGCTCTTATT | 227334 |
rs30309413 | snp | A/G | 0.32 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:87996445 | TTATGCTTACAACAA[A/G]ACATTTACAAGCCAG | 227334 |
rs30310194 | snp | A/C | 0.46875 | 0.121031 | intron-variant | Usp40 | Mm_Celera | 1:87995650 | GAGAAATCCTACAAC[A/C]AACTGAGTATTCGAA | 227334 |
rs30310195 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Usp40 | Mm_Celera | 1:87995059 | AACAACATCAGGTGG[C/T]AGTCAAAATTGCTGA | 227334 |
rs30310196 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:87995038 | CCACTAAGCTAACCA[C/T]CTCTGAACAACATCA | 227334 |
rs30310197 | snp | C/T | 0.489796 | 0.070696 | intron-variant | Usp40 | Mm_Celera | 1:87994920 | TGTAATTTTTCCCCA[C/T]TGTTATTGGAGTTTA | 227334 |
rs30310198 | snp | G/T | 0.197531 | 0.244432 | intron-variant | Usp40 | Mm_Celera | 1:87994911 | TAAATCTAATGTAAT[G/T]TTTCCCCATTGTTAT | 227334 |
rs30310199 | snp | A/G | 0.165289 | 0.235211 | intron-variant | Usp40 | Mm_Celera | 1:87994115 | CAACAGAATTCTGTA[A/G]CAGGAATAGAAATGC | 227334 |
rs30310200 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:87993962 | GAGGTCAACTAGTGT[A/G]TGAGAGTCTATACCA | 227334 |
rs30310201 | snp | C/G | 0.260355 | 0.249785 | intron-variant | Usp40 | Mm_Celera | 1:87993805 | GTGCTACTGAAAAAG[C/G]CTGTAACAGGCAATG | 227334 |
rs30310202 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp40 | Mm_Celera | 1:87993464 | AAACAGATAACACAA[A/G]ATCAAACCACCAGAT | 227334 |
rs30310203 | snp | A/C | 0.33241 | 0.236027 | intron-variant | Usp40 | Mm_Celera | 1:87993373 | GCCTAAAGTTCCTGC[A/C]CTTGAGAGACAGGCA | 227334 |
rs30310994 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Usp40 | Mm_Celera | 1:87993334 | TCAATAAATTAGCAA[C/T]TGGGTGTGACAGCCA | 227334 |
rs30310995 | snp | C/T | 0.32 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:87993327 | CAGAATTTCAATAAA[C/T]TAGCAATTGGGTGTG | 227334 |
rs30310996 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:87993018 | AAGTATCTAAGAATG[A/G]CCTCATTAGCATCAC | 227334 |
rs30310997 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Usp40 | Mm_Celera | 1:87992943 | GGTCGAAAGGTGGGG[C/T]TGCCAAATTTCACTC | 227334 |
rs30310998 | snp | C/G | 0.489796 | 0.070696 | intron-variant | Usp40 | Mm_Celera | 1:87992195 | CAACTACAACTTTCT[C/G]GAACAATGTACACAA | 227334 |
rs30310999 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Usp40 | Mm_Celera | 1:87991410 | AACCATAACAGCTAA[C/T]GGATAGCATTAAGAT | 227334 |
rs30311000 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:87990991 | GTCCTTTGGTAGACA[A/T]TTTTTGTTGATTTGT | 227334 |
rs30311001 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Usp40 | Mm_Celera | 1:87990918 | CTACCAATTTTTTGT[A/T]AACCCAACTTAAATT | 227334 |
rs30311002 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Usp40 | Mm_Celera | 1:87990281 | TGCAAGCTAGAGAAT[C/T]AGGCAGACCTGGCTT | 227334 |
rs30311003 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:87990201 | TTCACAGATGCCAGT[C/T]TAAAGGAATTAACCA | 227334 |
rs30311794 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Usp40 | Mm_Celera | 1:87989376 | TCAAGGCCACAGGTT[A/C]AAATTCTCTTCTGTT | 227334 |
rs30311795 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Usp40 | GRCm38.p3 | 1:87989317 | TATGGTGAACCTTTA[A/G]TCCCCAGTGCTTCAG | 227334 |
rs30311796 | snp | A/C/G | 0.142012 | 0.225474 | intron-variant | Usp40 | GRCm38.p3 | 1:87989282 | AGAATAAACAAAGCC[A/C/G]ATGTGGCTGACACAG | 227334 |
rs30311797 | snp | A/G | 0.18 | 0.24 | intron-variant | Usp40 | Mm_Celera | 1:87989273 | GATTTTGGAAGAATA[A/G]ACAAAGCCGATGTGG | 227334 |
rs30311798 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Usp40 | Mm_Celera | 1:87989176 | CTTGATTTGAAAATC[C/T]ATTTGTGAAGGGTTA | 227334 |
rs30311799 | snp | G/T | 0.429688 | 0.173817 | intron-variant | Usp40 | Mm_Celera | 1:87989126 | AATCAGAGCCATATA[G/T]TTTTAAAGGAACCTT | 227334 |
rs30311800 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Usp40 | Mm_Celera | 1:87987861 | ATGGAAGCTAATCTG[G/T]AAGCTCAGGCAGTCC | 227334 |
rs30311801 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:87986587 | GAAAACTGGGAAGAA[A/C]AAACACTTCTGAACT | 227334 |
rs30311802 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon, nc-transcript-variant | Usp40 | Mm_Celera | 1:87986137 | GGTAAGATGGTTCCT[C/T]AGGAGACTAACTGTA | 227334 |
rs30551711 | snp | C/T | 0.375 | 0.216506 | intron-variant | Usp40 | Mm_Celera | 1:87971667 | AGTTCATAATTTGCT[C/T]TTTCAAATGTCCTTT | 227334 |
rs30553778 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:87963533 | TTCAGGTAAATAAGA[A/G]AGCTTTAACTTTGAT | 227334 |
rs30574485 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp40 | Mm_Celera | 1:88005451 | ACGTTCTCTCCACAT[A/G]CTCATGGCCTGCCTC | 227334 |
rs30662440 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:88004061 | GGAGCATGATGGAGG[A/G]AGGACATCAACCCCT | 227334 |
rs30845106 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Usp40 | Mm_Celera | 1:87946901 | AACCACCATGTGTGT[A/G]CTGAGAACTGAAGTT | 227334 |
rs30861489 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Usp40 | Mm_Celera | 1:87955750 | ACACTTAGGAGAGAA[G/T]AATTTGACTGATTTA | 227334 |
rs30955958 | snp | A/G | 0.32 | 0.24 | intron-variant, nc-transcript-variant | Usp40 | Mm_Celera | 1:87947132 | TCTCTGTGTAGCCCT[A/G]GCTGTCCTGGAACTC | 227334 |
rs30958747 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Usp40 | Mm_Celera | 1:87966685 | TCCCAACTCTTAATG[A/G]CACCACGTAATTATT | 227334 |
rs31053385 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:87968926 | TGGTTCGGGAAAAGA[A/G]AAAAAGTAAAATAAA | 227334 |
rs31141435 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Usp40 | Mm_Celera | 1:87958160 | AATCCAAACATGGAA[C/T]ATGAGTTTAAAACAC | 227334 |
rs31178603 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Usp40 | Mm_Celera | 1:88009366 | TGTCTTATGGTACTT[C/T]ATCCTCCTATTTAAA | 227334 |
rs31209559 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp40 | Mm_Celera | 1:88002676 | GGATTCGGTCCTTTG[A/G]AAATTCTATTCAGTC | 227334 |
rs31229746 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp40 | Mm_Celera | 1:87979754 | GAGACATGGTTTCAT[A/G]CTGCCCAGGTTGGCC | 227334 |
rs31241629 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Usp40 | Mm_Celera | 1:88009487 | AGCTATATCCCCTTA[C/T]ACCCATGTGCTTGTT | 227334 |
rs31395119 | snp | A/G | 0.375 | 0.216506 | intron-variant | Usp40 | Mm_Celera | 1:87990857 | CAAAATACTCTTTTT[A/G]GCTTCACTGCTAAGT | 227334 |
rs31462494 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Usp40 | Mm_Celera | 1:87962085 | ATAGAGTTTTTTTGT[A/G]TGCTAAGAAAGAATA | 227334 |
rs31495965 | snp | G/T | 0.456747 | 0.140554 | intron-variant | Usp40 | Mm_Celera | 1:87977535 | AATAGTGACTAAAAC[G/T]GCATCCTACTGAGGG | 227334 |