SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3718577 | snp | G/T | 0.277778 | 0.248452 | intron-variant | Stac | Mm_Celera | 9:111563030 | TGACTCCCTGGAGAC[G/T]CAGTGTAAGGGCAGA | 20840 |
rs3719690 | snp | C/T | 0.235537 | 0.249581 | intron-variant | Stac | Mm_Celera | 9:111563169 | AAATAAGCATAAGCA[C/T]CTCTCATATTCCAGA | 20840 |
rs29590874 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Stac | GRCm38.p3 | 9:111659030 | CCAGTTAATCTGTTC[C/T]GTGCTTCTCATCTCC | 20840 |
rs29591650 | snp | G/T | 0.188366 | 0.242283 | utr-variant-3-prime | Stac | Mm_Celera | 9:111562057 | AGGACGCCCTCGTTC[G/T]CGATCTGTAGGTAAG | 20840 |
rs29604604 | snp | C/T | 0.415225 | 0.187619 | intron-variant | Stac | GRCm38.p3 | 9:111568620 | ATATCATCGCTATTC[C/T]CTTTCTTCCCTCATC | 20840 |
rs29639594 | snp | A/G | 0.375 | 0.216506 | intron-variant, downstream-variant-500B | Stac, Gm36088 | Mm_Celera | 9:111579392 | TCTCTCTCTGTCTCT[A/G]TCTGTCTGTCTCTGT | 20840 |
rs29640551 | snp | C/T | 0.375 | 0.216506 | utr-variant-3-prime | Stac | GRCm38.p3 | 9:111562000 | CTGCTGGACTCTGTG[C/T]CTTGGACCTTGCCCT | 20840 |
rs29641278 | snp | A/C | 0.42 | 0.183303 | intron-variant | Stac | GRCm38.p3 | 9:111657810 | TCACAGATACCATTA[A/C]ACTTGCACATTGTGT | 20840 |
rs29644688 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Stac | GRCm38.p3 | 9:111655924 | ATCAACTGAACAAAG[A/G]ATGGCTTGCTGGAAA | 20840 |
rs29686029 | snp | C/T | 0.255 | 0.24995 | intron-variant | Stac | Mm_Celera | 9:111563725 | GACCCTTCTTTAAAA[C/T]GGGGTGAGGCTATTT | 20840 |
rs29687176 | snp | C/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111643034 | ACCAGCATGTGCTTG[C/G]TCTTCCCAAGTCTGA | 20840 |
rs29694790 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111680589 | GGACTTATATTTCCA[C/T]GCCACCAATCATTAT | 20840 |
rs29704607 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630420 | GCTCAAAGGCACACA[A/G]TACTGCTTGCTTCAC | 20840 |
rs29740886 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111657867 | TTGTTTTTGAGACAG[A/G]GTTTCTCTGTGTATC | 20840 |
rs29786244 | snp | C/G | 0.42 | 0.183303 | intron-variant | Stac | Mm_Celera | 9:111630444 | GCTTCACTCACATTT[C/G]TATGCAAGGTTGGGT | 20840 |
rs29787724 | snp | A/T | 0.345679 | 0.230967 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111572881 | TTATATTGTTTAGTA[A/T]TTATTAAAGCCAGTC | 20840 |
rs29790945 | snp | C/T | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111567406 | AGAATCAATTTTCTC[C/T]GACCTCTCTGTTAAT | 20840 |
rs29829417 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111686346 | GAGGGACCAAACTTG[A/G]AACTTCATGTTTGCC | 20840 |
rs29832210 | snp | A/G | 0.401235 | 0.199068 | intron-variant | Stac | GRCm38.p3 | 9:111630988 | AATCCACAAGGAGAG[A/G]AAGCCAGCTCAGTAG | 20840 |
rs29840071 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111681566 | CAGTCATTACCCAGC[C/T]TTGGTCTGTACTTTA | 20840 |
rs29893423 | snp | C/T | 0.231111 | 0.249285 | utr-variant-3-prime | Stac | Mm_Celera | 9:111562610 | CGCTGGCCTCCTGCT[C/T]GGGAAGGGACTGCTA | 20840 |
rs29894639 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111680690 | GTTGCTTCCTTGCTT[A/G]CTTCCAGTACCTTGT | 20840 |
rs29894870 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630434 | AATACTGCTTGCTTC[A/G]CTCACATTTGTATGC | 20840 |
rs29931056 | snp | A/C | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111642932 | GGGCATCCTGAGAGC[A/C]CATGGAGAATTTAGC | 20840 |
rs29976442 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Stac | GRCm38.p3 | 9:111659233 | TTTGCCCAGATACTG[C/T]CAATCGAATGTTCAT | 20840 |
rs29991570 | snp | G/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111686148 | GAGTACACCCCCAGG[G/T]GTAGGTCATCCTCCG | 20840 |
rs30029242 | snp | G/T | 0.18 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111656382 | ACTTCCTGAGGGTCA[G/T]GTAGGGTCTTTCTGT | 20840 |
rs30035713 | snp | C/T | 0.444444 | 0.157135 | upstream-variant-2KB | Stac | GRCm38.p3 | 9:111691170 | TGAATACTAGACTCC[C/T]TCCTTATTTTTATGT | 20840 |
rs30037404 | snp | C/T | 0.18 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111563757 | AGGACTTAATTTCTT[C/T]GCAACTCTCTTTTCC | 20840 |
rs30043201 | snp | A/G | 0.484429 | 0.0868505 | intron-variant | Stac | Mm_Celera | 9:111632921 | TGCTTGAGGTGTCCT[A/G]AGAACCCCACTAAGG | 20840 |
rs30076591 | snp | G/T | 0.345679 | 0.230967 | intron-variant | Stac | Mm_Celera | 9:111630628 | TTCTGGACACCAAAA[G/T]ACTATTGCATCCACT | 20840 |
rs30090389 | snp | A/C | 0.375 | 0.216506 | intron-variant, nc-transcript-variant | Stac, Gm36088 | Mm_Celera | 9:111573063 | ACTGTCTGTAGCTTC[A/C]GGTCCAGAGGATCTG | 20840 |
rs30090664 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111659559 | ACAATACAGACAATG[A/C]ATTTTACATCTGGAT | 20840 |
rs30092135 | snp | A/G/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111568803 | CAGAGGCCCATGCTT[A/G/T]TACTCTTGCCCGGCG | 20840 |
rs30127106 | snp | A/G | 0.486111 | 0.0821678 | intron-variant | Stac | GRCm38.p3 | 9:111631165 | TCTTGAGTGGTGGTG[A/G]TGATGATGATGGTGG | 20840 |
rs30130381 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Stac | Mm_Celera | 9:111683899 | ACTGGTACTCTATGC[A/G]TACGTGTGTCGATTG | 20840 |
rs30135725 | snp | A/G | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111568877 | ACTCTATTTTGTAAA[A/G]TAGAAATACTGCATG | 20840 |
rs30137197 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Stac | GRCm38.p3 | 9:111630956 | GACTGGCTGGAGGGC[A/G]AGGCTTAGATCTGCT | 20840 |
rs30169579 | snp | A/C | 0.345679 | 0.230967 | intron-variant | Stac | Mm_Celera | 9:111567374 | ATGTTATAAAAAAAA[A/C]CACGGCATTCATTTT | 20840 |
rs30173635 | snp | A/C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111680581 | TCTTGTTTGGACTTA[A/C/T]ATTTCCATGCCACCA | 20840 |
rs30177252 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111664105 | AATTTTTGGGGTCAC[C/T]TATATATACTATCAT | 20840 |
rs30182024 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | Mm_Celera | 9:111655347 | GCTTAAAGTGGCTTC[A/G]CTCAGCACCTGGGGG | 20840 |
rs30229969 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111636565 | CAGCTTTGAGGTGGG[C/T]TCCTTTGGTTAAGTA | 20840 |
rs30232189 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111616901 | ATCTATCTATCTATC[C/T]ATCCATCCATCCATC | 20840 |
rs30277978 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630717 | GGGGCTCACAGCAAG[A/G]TTTTTGTTTGTTTGT | 20840 |
rs30321940 | snp | G/T | 0.207612 | 0.24638 | intron-variant | Stac | Mm_Celera | 9:111581793 | CAAACCTAGTCCCGA[G/T]AGACTTCTCAGAGTG | 20840 |
rs30423144 | snp | G/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111643086 | CCCGCACAGGCAGCA[G/T]CCTGCGAGGCATACA | 20840 |
rs30425218 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111658261 | TGGGTTTTCCATCTT[C/T]ATTTGCTGCTAAGCA | 20840 |
rs30431581 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111604362 | GAACTTGATACTTGG[A/G]GAACTTGATACCAAC | 20840 |
rs30468189 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Stac | GRCm38.p3 | 9:111562469 | CTGCTCTCAGGACGC[C/T]TTGATGTGCTGTGCA | 20840 |
rs30477832 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | Mm_Celera | 9:111685106 | GGGACGTCATGTCAG[C/T]AACTTACTCTTCTTT | 20840 |
rs30477861 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Stac | GRCm38.p3 | 9:111635286 | GTGAGCAGGGAGAGG[C/T]TCCACATGACCCATT | 20840 |
rs30482498 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Stac | Mm_Celera | 9:111659723 | ATCTCTTAGTCACGT[A/G]CACTATTAATGTCAA | 20840 |
rs30518159 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111635336 | CCTTGCTTTCTTAGG[C/T]CCCACCAATGTGCTG | 20840 |
rs30519269 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Stac | Mm_Celera | 9:111658195 | CAACATGCATTTGAA[A/G]GGAAAGACAAAGATC | 20840 |
rs30761993 | snp | A/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111668876 | GTGGAAAACCCTGTG[A/T]CTGGAAAAGCCTAGA | 20840 |
rs30820134 | snp | A/G | 0.207612 | 0.24638 | intron-variant | Stac | GRCm38.p3 | 9:111671225 | AGTGATGGATATGGC[A/G]CTTAAATATCCCTTG | 20840 |
rs30858310 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111677263 | TGCGAGGAATAGAGC[A/G]GGGGAGGTGATTCTG | 20840 |
rs30874687 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Stac | GRCm38.p3 | 9:111668895 | AAACCTGGAATTCAC[A/G]TGAGTGGAAAACCCT | 20840 |
rs30960812 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111677438 | TTCTGTAGGACATTG[C/T]GTCAAGTAGAAGAAG | 20840 |
rs30973803 | snp | A/G | 0.429688 | 0.173817 | intron-variant | Stac | GRCm38.p3 | 9:111672477 | TATTAGGGGGGCGGT[A/G]TATGTGTTTGGTATA | 20840 |
rs31014394 | snp | C/T | 0.5 | 0 | intron-variant | Stac | GRCm38.p3 | 9:111672623 | AAACAAAACCCACCC[C/T]CACCAAAAATCCAAC | 20840 |
rs33630412 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111564213 | GTTATAGGAATGGAA[C/T]GTTATGTACGCTGCC | 20840 |
rs33644814 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | Mm_Celera | 9:111632868 | TCAGATAAAATCACA[A/G]CACAACCTTCTTTAG | 20840 |
rs33644821 | snp | A/G | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111651969 | AAAGCTGGGGGGAGC[A/G]TACAATAGAGACATA | 20840 |
rs33648891 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Stac | GRCm38.p3 | 9:111630981 | TCTGCTCAATCCACA[A/G]GGAGAGGAAGCCAGC | 20840 |
rs33655573 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | Mm_Celera | 9:111642913 | ATTAGGAAGCACAGA[C/T]ATTGGGCATCCTGAG | 20840 |
rs33656426 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Stac | Mm_Celera | 9:111565015 | TCAGCTCCTGCTTGA[C/G]TTCCAGTCCTGACTT | 20840 |
rs33658602 | snp | A/G | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111568536 | GCCTCTACCTCCCAA[A/G]CACTGAGGTGCCAGA | 20840 |
rs33661759 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111631163 | AATCTTGAGTGGTGG[C/T]GGTGATGATGATGGT | 20840 |
rs33676918 | snp | C/T | 0.197531 | 0.244432 | intron-variant | Stac | Mm_Celera | 9:111658043 | AAAAAAATCCACATG[C/T]TAGGTATCAGGGTGG | 20840 |
rs33702092 | snp | A/G | 0.46281 | 0.131194 | intron-variant | Stac | GRCm38.p3 | 9:111653318 | ATGAGTGAATGTTAC[A/G]ATTTTTTTAAAAAAG | 20840 |
rs33702690 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111633186 | TGAGCATGGAGCATG[A/C]CGGGACCCCCTCTGG | 20840 |
rs33739020 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Stac | GRCm38.p3 | 9:111630905 | CCCCAGCACCCCCAC[C/T]ATCACCCCAATAGAC | 20840 |
rs33740926 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Stac | GRCm38.p3 | 9:111635252 | GGACTCAGTAGTTCA[C/T]CCTGTATCCCATAAG | 20840 |
rs33748344 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Stac | Mm_Celera | 9:111642850 | CCAGCTGGGATTTTA[A/G]CAGTGGTCTACACAG | 20840 |
rs33750397 | snp | C/T | 0.375 | 0.216506 | upstream-variant-2KB | Stac | Mm_Celera | 9:111692208 | AATAGGATTAGCGAT[C/T]GATAATGATGTCTTC | 20840 |
rs33752617 | snp | G/T | 0.475309 | 0.108333 | intron-variant | Stac | Mm_Celera | 9:111630691 | CCTGCAGAAGATGTA[G/T]GGATAGGAATGGGGC | 20840 |
rs33767311 | snp | C/G | 0.5 | 0 | intron-variant | Stac | Mm_Celera | 9:111681729 | AAAGAGGAGCATCAA[C/G]AAACTGGACCACGTG | 20840 |
rs33776067 | snp | C/T | 0.304688 | 0.243945 | intron-variant | Stac | Mm_Celera | 9:111567410 | TCAATTTTCTCTGAC[C/T]TCTCTGTTAATGGCC | 20840 |
rs45646585 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Stac | GRCm38.p3 | 9:111627855 | TTATCAAAGCTGATC[G/T]CGTCTTTGAGGAATT | 20840 |
rs45649217 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111606099 | GATGGGGTTTGGGCA[C/T]AGAAGTGGCTCCCTA | 20840 |
rs45654564 | snp | C/T | | | intron-variant | Stac | GRCm38.p3 | 9:111634263 | CATGAACCATTGACT[C/T]ATAGTATCGGGGTAG | 20840 |
rs45656925 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Stac | GRCm38.p3 | 9:111630467 | GGTTGGGTTGTCTAT[A/C]ATAGCTTGAATAGGT | 20840 |
rs45662770 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111655097 | GCTGATGTCTGACGG[C/T]GAAATGTTGGGTTGG | 20840 |
rs45674404 | snp | A/G | | | intron-variant | Stac | Mm_Celera | 9:111641085 | CCAGAGGTCTGAGAT[A/G]CTCATTTAAAATTCA | 20840 |
rs45674864 | snp | C/T | | | intron-variant | Stac | Mm_Celera | 9:111642468 | TCCTAGCTGCCTGGA[C/T]GTAAGTCTTCTCCTG | 20840 |
rs45676138 | snp | A/G | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111685615 | AAAACACCTGGAATG[A/G]ATGCTCTCTTCTGTT | 20840 |
rs45679354 | snp | A/C | 0.277778 | 0.248452 | intron-variant | Stac | GRCm38.p3 | 9:111643623 | GACACACCCAAGGCT[A/C]GTGGGCAGACACAGT | 20840 |
rs45681747 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Stac | Mm_Celera | 9:111636484 | TCAGCCCTTAGCACC[C/T]GCCTTTCTGCCACCC | 20840 |
rs45691125 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111583087 | TCAAACAAGAGACAA[A/C]TCCCTGAGAAAACAT | 20840 |
rs45697149 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Stac | Mm_Celera | 9:111629565 | TAAAAATGTAAAAGC[A/G]TGTAATAAAAAATGG | 20840 |
rs45707689 | snp | A/G | | | intron-variant | Stac | GRCm38.p3 | 9:111610340 | ATAGGAAGTGTAGAC[A/G]TGAGTTTAATATTTA | 20840 |
rs45710372 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111671178 | TGCTGCCTTGTGGTT[A/G]ATGCTCTGTTCCTAG | 20840 |
rs45711323 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Stac | GRCm38.p3 | 9:111674423 | TCTTTTCATTTTCTC[A/G]AAGTCACTTTGGAAG | 20840 |
rs45719633 | snp | C/T | 0.375 | 0.216506 | intron-variant | Stac | GRCm38.p3 | 9:111609110 | GGTCTGGTCGGACCT[C/T]GATCTGCTACACCTG | 20840 |
rs45728575 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111630969 | GCGAGGCTTAGATCT[C/G]CTCAATCCACAGGGA | 20840 |
rs45737768 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111684991 | GACTACACACGCTTA[C/T]AGGAATTGGCTCTGA | 20840 |
rs45739527 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Stac | Mm_Celera | 9:111660533 | TGTGGGAAGAGAGAA[A/G]AAGGATCTTGTTGAA | 20840 |
rs45744730 | snp | C/T | 0.32 | 0.24 | intron-variant | Stac | GRCm38.p3 | 9:111673996 | ACACGGAAGCAGAAG[C/T]GAATCTGTGTCCCTC | 20840 |