SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3674030 | snp | C/G | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19684718 | CACCTCACACTCAGT[C/G]TGAGAATGCAGACTC | 381485 |
rs3675721 | snp | A/C | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19684961 | CTTCTGTCGATTTCA[A/C]AACTGGTAACTGGCT | 381485 |
rs3675805 | snp | A/G | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19685016 | CTCCTTCAAGGGTGT[A/G]TAGTACATAAGCTAT | 381485 |
rs6264230 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Trim55 | Mm_Celera | 3:19673131 | AGATCAGGACAGTTA[C/T]AATGCCAGAGAGAAA | 381485 |
rs6264662 | snp | A/G | 0.471655 | 0.115624 | intron-variant | Trim55 | Mm_Celera | 3:19673185 | CTCATCACCATTATT[A/G]TGGTTAGCAAGATTT | 381485 |
rs6317109 | snp | A/T | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19669422 | tgccacagccatgtc[A/T]tgtctatgagacacc | 381485 |
rs6318054 | snp | C/T | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19669557 | cttagggccaatcaa[C/T]ccccacttattctca | 381485 |
rs6318576 | snp | C/G | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19669658 | ACTGAAGTTTaggaa[C/G]ctcatgactggtact | 381485 |
rs6318648 | snp | A/G | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19669696 | tgatctaagggtcat[A/G]tctggggaggtcata | 381485 |
rs6319734 | snp | C/T | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19669912 | TGTGGTGACTATATG[C/T]CTCATGAATNTATGT | 381485 |
rs6319750 | snp | C/T | 0.207612 | 0.24638 | intron-variant | Trim55 | Mm_Celera | 3:19669922 | ATATGNCTCATGAAT[C/T]TATGTTACATCACAA | 381485 |
rs6320218 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Trim55 | GRCm38.p3 | 3:19669944 | ACATCACAATTAACC[A/G]TCCAGCTCTCCCATT | 381485 |
rs6400173 | snp | A/T | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19647384 | atgcaataacaattt[A/T]aaaagagtcnatgag | 381485 |
rs6400186 | snp | C/T | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19647394 | aatttnaaaagagtc[C/T]atgagtttgaaagat | 381485 |
rs6400725 | snp | A/C | 0.32 | 0.24 | intron-variant | Trim55 | Mm_Celera | 3:19647486 | AAGAGATAATCCTGG[A/C]AACTAGTAAGCAACC | 381485 |
rs6400785 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim55 | Mm_Celera | 3:19647514 | ACCAGTTATTAAAAG[A/G]CATTTCTGTGACAGC | 381485 |
rs6401308 | snp | C/G | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19647618 | CAAGCATAGTACAGT[C/G]TTCTGTGTTTTATTT | 381485 |
rs6401835 | snp | A/T | 0.408163 | 0.193609 | intron-variant | Trim55 | Mm_Celera | 3:19647720 | TTTGGTATGAAATCT[A/T]GAGGACAGAAAATGT | 381485 |
rs13477004 | snp | C/T | 0.408163 | 0.193609 | utr-variant-5-prime | Trim55 | GRCm38.p3 | 3:19644554 | ACCACTTACAGAAGC[C/T]GTTCGGGAGCACCTT | 381485 |
rs30012401 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim55 | GRCm38.p3 | 3:19661038 | CATGTATCTACACTG[C/T]ATTAGCATAGTAGGA | 381485 |
rs30058877 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim55 | GRCm38.p3 | 3:19687833 | TTTTGACCAAATTCC[A/G]TCAAGAGTTGAGACA | 381485 |
rs30104061 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim55 | Mm_Celera | 3:19658371 | TTGTAGTGTGTGTGT[G/T]TGTGTGTGTGTGTGT | 381485 |
rs30266272 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Trim55 | GRCm38.p3 | 3:19677357 | TCTGGTGCAACTTCA[A/G]TACACAGAACCACTA | 381485 |
rs30310398 | snp | A/G | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19685633 | ATGGGTCACGGTCAT[A/G]AGTGGCACAGAGATC | 381485 |
rs30359943 | snp | G/T | 0.432133 | 0.171253 | intron-variant | Trim55 | GRCm38.p3 | 3:19674052 | CTTTGCTCCATCTGC[G/T]CTACCATCTAGTGGA | 381485 |
rs30414578 | snp | A/T | 0.375 | 0.216506 | intron-variant | Trim55 | GRCm38.p3 | 3:19691443 | CAAAGGTCTACTCTC[A/T]CCTTCCTCTCATCCA | 381485 |
rs30505647 | snp | G/T | 0.492188 | 0.0620098 | intron-variant | Trim55 | GRCm38.p3 | 3:19658208 | TTTTTAAGAAACGTA[G/T]TTCAATGGCAATGGG | 381485 |
rs30517792 | snp | A/G | 0.32 | 0.24 | intron-variant | Trim55 | Mm_Celera | 3:19691059 | ACTCGGGCCTAGGAC[A/G]GCTGGGAAGGCACTC | 381485 |
rs30561983 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19649366 | GTAAAGGCCAAAAGA[C/G]AGTGTCAGGTCCTCT | 381485 |
rs30601493 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19644860 | AGTTCCCTTAGAGAG[C/T]TTTCTGAGACTGTTC | 381485 |
rs30606010 | snp | C/T | 0.32 | 0.24 | intron-variant | Trim55 | Mm_Celera | 3:19691216 | AAGCCAAGCAGGGAA[C/T]CCTGGCTTCTCCCCA | 381485 |
rs30654254 | snp | C/T | 0.48 | 0.0979796 | downstream-variant-500B, upstream-variant-2KB | Trim55, LOC105247005 | Mm_Celera | 3:19692682 | GAGAAGTGCCATCTT[C/T]ATATATACAAATTAA | 381485 |
rs30660811 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19656949 | TGTTGCTGATGCGCG[A/C]ATCTATGTTTCCTGA | 381485 |
rs30660973 | snp | C/G | 0.465374 | 0.126941 | intron-variant | Trim55 | Mm_Celera | 3:19679219 | AAAACCTTCAAATGA[C/G]TAAGTTTGTCACCTT | 381485 |
rs30700518 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim55 | Mm_Celera | 3:19691330 | CTAAGATGACCTAAG[C/T]TTGCTTTCTATCCCT | 381485 |
rs30701179 | snp | A/G | 0.493827 | 0.0552116 | synonymous-codon | Trim55 | GRCm38.p3 | 3:19671551 | GGAAGCATCAAAGGC[A/G]TTTCAGATGGAGAAA | 381485 |
rs30722456 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim55 | GRCm38.p3 | 3:19686245 | GCCCAGGTGACAGAC[A/G]TATGTTGACGCCGGC | 381485 |
rs30751741 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19679753 | ATGATTTACCGTTCA[C/G/T]AATGTGGCTGGTGAA | 381485 |
rs30759976 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Trim55 | GRCm38.p3 | 3:19658192 | CCATATAATCCTGTG[C/G]TTTTTAAGAAACGTA | 381485 |
rs30811751 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19678783 | TTTAAAATGTTTCTG[C/T]TACCTTTCAATTTTA | 381485 |
rs30842553 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19648808 | AGGCCTTTAGTGAGA[A/C]GGGTTGTTCCAATCT | 381485 |
rs30859442 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Trim55 | GRCm38.p3 | 3:19686218 | CAACAAAGTAGTATC[A/G]GTGACAAACAGGCCC | 381485 |
rs30886786 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19677589 | CCATGCCCAGCTCTG[C/G]TCTTCTCTTAAATAT | 381485 |
rs30894534 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Trim55 | GRCm38.p3 | 3:19675127 | ACTGATAAAAAAAAA[A/T]TTAATGATATGGCCT | 381485 |
rs30990865 | snp | A/G | 0.375 | 0.216506 | intron-variant | Trim55 | Mm_Celera | 3:19691402 | CATCCTCTCTCCTCC[A/G]TAGATCAGTAACTGG | 381485 |
rs30999964 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim55 | GRCm38.p3 | 3:19665595 | GGCCAGGCTCAGGCT[C/T]TATCTTCAGGCTATT | 381485 |
rs31003060 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Trim55 | GRCm38.p3 | 3:19680087 | CTTAATAACAAAACT[C/T]ATCTGTTTTCTGCTC | 381485 |
rs31003785 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trim55 | GRCm38.p3 | 3:19656301 | TGGTAAGTTTTCATC[C/G]TTGTGTTGGTGTTTT | 381485 |
rs31035731 | snp | C/G | 0.49827 | 0.0293608 | intron-variant | Trim55 | GRCm38.p3 | 3:19650463 | ATTGGTGACTTTAGA[C/G]CCATGTTGCCCCTAA | 381485 |
rs31113899 | snp | C/T | 0.465374 | 0.126941 | intron-variant | Trim55 | GRCm38.p3 | 3:19661266 | TTTTCTTTGTGTTTT[C/T]AACAGAATCTAGTTC | 381485 |
rs31145198 | snp | C/G | 0.375 | 0.216506 | intron-variant | Trim55 | Mm_Celera | 3:19690914 | CGTCAGCAGTGGAGA[C/G]ATTATATGAATATGA | 381485 |
rs31145247 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Trim55 | GRCm38.p3 | 3:19686366 | TCTGCAGGAGGGAGG[C/T]GAAGTTTGCAGGATG | 381485 |
rs31230576 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19673469 | TCCTGAGGCACCTTT[G/T]CCTTCTCCTCGGAGA | 381485 |
rs31240776 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19684221 | CCTGGGATCTCTGTG[A/T]CCAAGAAGCCCTCTA | 381485 |
rs31267344 | snp | C/T | 0.486111 | 0.0821678 | intron-variant | Trim55 | GRCm38.p3 | 3:19646411 | GCTGGTTCCCTGCTA[C/T]ACAATACTCTTTGCA | 381485 |
rs31292564 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim55 | GRCm38.p3 | 3:19660470 | ACCATGATTTGTATT[C/T]GTTGGTGTTATTTAT | 381485 |
rs31329626 | snp | C/G | 0.487535 | 0.077957 | intron-variant | Trim55 | GRCm38.p3 | 3:19672640 | ACAAGATTTCAACAT[C/G]GTAGACCTGGTCCAT | 381485 |
rs31339228 | snp | G/T | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19688003 | AGAGGGAGAAGAGAA[G/T]CAGAGAAGTAAGAAA | 381485 |
rs31342036 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19652953 | GTTTAGGAATTTTTT[C/T]CCCTGTGCCCATATC | 381485 |
rs31380350 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Trim55 | GRCm38.p3 | 3:19660349 | TCAGTAGGCCCATCA[C/T]GCCTCAGTTTCTTCC | 381485 |
rs31385002 | snp | A/C | 0.375 | 0.216506 | intron-variant | Trim55 | Mm_Celera | 3:19686555 | AAACAAACAAAAAAA[A/C]AAAAAAAAAAAAACC | 381485 |
rs31429358 | snp | A/G | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19653476 | AGATTGCTTTCGGCA[A/G]GATAACCATTTTGAC | 381485 |
rs31432251 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Trim55 | Mm_Celera | 3:19674209 | CTTTTTCTTCTTCTT[C/T]TTTTTTTTTTTTTTT | 381485 |
rs31435187 | snp | A/G | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19667848 | ATTTTAGTAGGTAGT[A/G]CATGCCTGTTCCTTA | 381485 |
rs31437461 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim55 | GRCm38.p3 | 3:19646412 | CTGGTTCCCTGCTAT[A/G]CAATACTCTTTGCAG | 381485 |
rs31438972 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Trim55 | GRCm38.p3 | 3:19686067 | GACACCTGTTAAGAG[C/G]TATGAGCTGTGACTG | 381485 |
rs31472278 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Trim55 | GRCm38.p3 | 3:19658754 | CCTCTTCTTCACCCA[C/T]AGGAAGATCGCGTGA | 381485 |
rs31488328 | snp | G/T | 0.5 | 0 | intron-variant | Trim55 | Mm_Celera | 3:19690671 | TTGGCTTTGCAAAAC[G/T]GAGGGGTTTTGCAAA | 381485 |
rs31542529 | snp | C/G/T | 0.5 | 0 | downstream-variant-500B | Trim55 | GRCm38.p3 | 3:19692391 | TCTCCCCCTGTGTGC[C/G/T]TTCTCTCTCTCTCTC | 381485 |
rs31572937 | snp | A/C | 0.375 | 0.216506 | intron-variant | Trim55 | Mm_Celera | 3:19686551 | AAACAAACAAACAAA[A/C]AAAAAAAAAAAAAAA | 381485 |
rs31589319 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Trim55 | GRCm38.p3 | 3:19680240 | AATAGTGTTGAAAAT[C/T]CTTGGGCGTTGTTCC | 381485 |
rs31595171 | snp | A/C | 0.5 | 0 | intron-variant | Trim55 | GRCm38.p3 | 3:19657582 | AGTCTCACTGGTCAG[A/C]GTACTCTCTGTAGGC | 381485 |
rs31596869 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim55 | Mm_Celera | 3:19691415 | CCGTAGATCAGTAAC[C/T]GGACCAATTCCCCAA | 381485 |
rs31614334 | snp | C/T | 0.375 | 0.216506 | intron-variant | Trim55 | GRCm38.p3 | 3:19688049 | GGAAGGGAGGGAGAG[C/T]TGATGGTGGCTCACA | 381485 |
rs31621374 | snp | A/C | 0.444444 | 0.157135 | synonymous-codon, utr-variant-3-prime | Trim55 | GRCm38.p3 | 3:19691557 | TCCTGAGCCAGCTCG[A/C]CACGTCTTCTCCTTC | 381485 |
rs31680518 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Trim55 | Mm_Celera | 3:19649872 | CAACCAGCAGAAATT[A/G]TCTAGCTGTTTCCAG | 381485 |
rs31694773 | snp | C/T | 0.5 | 0 | downstream-variant-500B, upstream-variant-2KB | Trim55, LOC105247005 | Mm_Celera | 3:19692494 | CCCTCCCTCCCCCCC[C/T]CCGTCTCTCTCTCTC | 381485 |
rs45641250 | snp | A/C | | | intron-variant | Trim55 | Mm_Celera | 3:19652809 | AGATTGAGAAAGGAT[A/C]TCTACCTATTCTAAG | 381485 |
rs45652155 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19675150 | TATGGCCTGATAAAC[G/T]TTTACTTTTATAATG | 381485 |
rs45657928 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19672589 | GCAAAGCAATGGTTC[A/T]TTCATATTTGCCCTA | 381485 |
rs45669257 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19660716 | GAGAAGACTGTAGGT[A/T]TCAAATGCCTTACAC | 381485 |
rs45687332 | snp | C/T | | | intron-variant | Trim55 | GRCm38.p3 | 3:19664177 | CATGGGAAGAATAGT[C/T]AGGAGGAAAATACTA | 381485 |
rs45700982 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19679126 | TGGTTGGTTGAACCT[G/T]CATGGGCCTCTCTCA | 381485 |
rs45706978 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19674003 | ACTTGCCATACGTGG[C/T]ATTGCATATACAACA | 381485 |
rs45708515 | snp | A/C/G | 0.48 | 0.0979796 | intron-variant | Trim55 | GRCm38.p3 | 3:19664991 | CTCATCAAGCCACAC[A/C/G]GTTTTCCTGAGTCTG | 381485 |
rs45769416 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19660109 | AACAATTTCTTGCCT[A/G]TGAGACTCATAATCA | 381485 |
rs45770422 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19660297 | TGTAGCAGCTGCCTA[A/G]AATTTATGCTTCTAT | 381485 |
rs45774259 | snp | A/G | | | intron-variant | Trim55 | Mm_Celera | 3:19663930 | ATAAAAGCTGGCTGA[A/G]GATAAAGAACAATTT | 381485 |
rs45780733 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Trim55 | Mm_Celera | 3:19673400 | CAGAACCTTGACTCT[C/T]GTGTCCATAATGGAG | 381485 |
rs45812077 | snp | A/C | | | intron-variant | Trim55 | GRCm38.p3 | 3:19669235 | AGAGGCAGCGAGACC[A/C]CCGGGGCCAGAGAGT | 381485 |
rs45820975 | snp | C/T | 0.459184 | 0.136902 | intron-variant | Trim55 | GRCm38.p3 | 3:19664907 | TGAGAACTCTAAATA[C/T]TGGTAGCAAGGGAGA | 381485 |
rs45832714 | snp | G/T | 0.495868 | 0.0452663 | intron-variant | Trim55 | GRCm38.p3 | 3:19645023 | AAATGTTACCGCTCA[G/T]GTCTGAGCATTGGAA | 381485 |
rs45861940 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Trim55 | Mm_Celera | 3:19649955 | TGCTTTATGTAGTTT[G/T]ATTTCCTTGGTCTTT | 381485 |
rs45863377 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19668098 | GAAGGCCGAATTTTC[A/G]CACTCCAGGGGAAGG | 381485 |
rs45867932 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19675656 | TCTCCACAAGTAACA[C/T]ATAGTAGATCTCCCA | 381485 |
rs45872338 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Trim55 | Mm_Celera | 3:19677274 | AACCTGATCATAATG[A/G]GAACCACTCTTGGAC | 381485 |
rs45902594 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Trim55 | Mm_Celera | 3:19649146 | CGCTCTCAACTCTCA[C/T]TTCCCAAATGCTAGA | 381485 |
rs45911804 | snp | A/C | 0.260355 | 0.249785 | intron-variant | Trim55 | Mm_Celera | 3:19661699 | CTTAGGAATAACACC[A/C]CTTTGAGGACAATGG | 381485 |
rs45927350 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Trim55 | Mm_Celera | 3:19676274 | CAGACTCTGCACTAG[C/G]CTAGGACTAGGGGAT | 381485 |
rs45949329 | snp | A/T | 0.497778 | 0.0332592 | intron-variant | Trim55 | GRCm38.p3 | 3:19651358 | ACCCATAGTGGACAG[A/T]ATGTTTTACATTGCA | 381485 |