SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3142415 | snp | G/T | | | intron-variant | Brsk2 | Mm_Celera | 7:141958193 | atatatatatatata[G/T]agagagagagagaga | 75770 |
rs6272657 | snp | C/T | 0.5 | 0 | intron-variant | Brsk2 | Mm_Celera | 7:141953293 | Cagaggagagatggg[C/T]gagggagaagggtga | 75770 |
rs6272708 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Brsk2 | Mm_Celera | 7:141953330 | agatcagaggacagg[C/T]gaaagacaggtggga | 75770 |
rs6273249 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Brsk2 | Mm_Celera | 7:141953412 | acaggtgtagaggaa[A/G]acaggtgagaATCAC | 75770 |
rs6273828 | snp | A/G | 0.415225 | 0.187619 | intron-variant, downstream-variant-500B | Brsk2, Mir3104 | Mm_Celera | 7:141992653 | TGCTTGAATGCTATC[A/G]CTGATCCTGGTTGCT | 75770 |
rs6322071 | snp | C/T | 0.5 | 0 | intron-variant | Brsk2 | Mm_Celera | 7:142001023 | ACAGGCATTGGACCA[C/T]CCACCACCCCTGGGC | 75770 |
rs6322685 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Brsk2 | Mm_Celera | 7:142001160 | TTGTGCTGGAAGGCA[A/G]TAAAGGGTCTACATG | 75770 |
rs31049838 | snp | G/T | 0.5 | 0 | intron-variant, downstream-variant-500B | Brsk2, Mir3104 | Mm_Celera | 7:141992684 | ATGTGTGCATGTGGG[G/T]GGGGTGGGCACGGGC | 75770 |
rs36239397 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141977696 | AGTGCCCAGCCCACA[C/T]GGCAGTGCCTTGCCC | 75770 |
rs36243236 | snp | A/C/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | GRCm38.p3 | 7:141982607 | TGGTGATAGCCTGTA[A/C/G]CCTGTAGAAGAGGAG | 75770 |
rs36249319 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141983427 | AGGGTAGATCTGTAG[C/T]TTTCCAGGGCCATTA | 75770 |
rs36263294 | snp | A/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141977806 | CTCTACCTGTAGTGA[A/G]GGTCACTATTGCTCA | 75770 |
rs36263395 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141979555 | TACCTGCCAGCCCTG[C/T]TCTTAGGCCATCCTT | 75770 |
rs36268234 | snp | A/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:142000520 | CCTTGCTCCCACTCA[A/G]CTGTAGTCATAGGCT | 75770 |
rs36270364 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Brsk2 | Mm_Celera | 7:141995632 | CCTGCAGCTTAGCCT[C/T]CCCTAGGGTCTCTGG | 75770 |
rs36271429 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141991419 | GGTGTTGCCTAGGTG[A/G]GAACCAGAAACCCAC | 75770 |
rs36277571 | snp | C/T | 0.408163 | 0.193609 | intron-variant | Brsk2 | Mm_Celera | 7:141965242 | CCAAGACCAAATGGA[C/T]GTCTGAAATTCTTGT | 75770 |
rs36278430 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Brsk2 | Mm_Celera | 7:141999459 | TAGTCTGTATAGCAA[C/T]GGGACAGGCTGATGG | 75770 |
rs36288736 | snp | C/T | 0.426035 | 0.177515 | intron-variant | Brsk2 | Mm_Celera | 7:141970957 | CAAATCCAGCTGACC[C/T]GACACTGGGATATTT | 75770 |
rs36303029 | snp | A/C | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141955366 | TGGGACTTTGTGAGG[A/C]TCCAAAACTGAATGT | 75770 |
rs36308733 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141968660 | TAAACTCCATTATCA[C/T]GCAAGTGTCCCCTGC | 75770 |
rs36320628 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Brsk2 | Mm_Celera | 7:141954033 | GAGTTCCTCTTCTCC[C/T]TGAGAGCTGTTTCTG | 75770 |
rs36323896 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141994950 | GGCCCTTCTCTCATG[C/T]ACCCTTATGGCTCAC | 75770 |
rs36335450 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brsk2 | Mm_Celera | 7:141960647 | CTGGAGGAGAGGAAC[A/G]CAGAGCCTGGTTTAG | 75770 |
rs36338567 | snp | A/C | 0.124444 | 0.216185 | utr-variant-3-prime | Brsk2 | Mm_Celera | 7:142002945 | GTTCTCATGGGCTGA[A/C]GTGGAGATAAAAGAC | 75770 |
rs36340063 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Brsk2 | Mm_Celera | 7:141957949 | TATGGAAACTGTGTG[C/T]CCAGTGCTGGGTCTG | 75770 |
rs36340170 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141980624 | AGAGGACCCCTGCTA[C/T]CTCCTCCAGCCTGCC | 75770 |
rs36365492 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141979915 | CAGTAGTATCCTTGC[C/T]CTCCTGTCTTTCTCC | 75770 |
rs36377383 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141990760 | TCTTTTATCCAGATG[A/G]TCTTGGTGTTATTCC | 75770 |
rs36383894 | snp | C/T | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141982813 | TGTCCTGGCATTGGC[C/T]CTTCCCAGACCTTCT | 75770 |
rs36388409 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Brsk2 | Mm_Celera | 7:141996305 | GGAGGAAGGTGTAGA[A/G]GGAGCTTGCCCAAAA | 75770 |
rs36389255 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141963765 | CTAGCTGCGGATGGG[A/G]CTTCACTGACATCAC | 75770 |
rs36389678 | snp | A/C | 0.152778 | 0.230321 | intron-variant | Brsk2 | Mm_Celera | 7:141967194 | CCCTTGGGTCCCAAA[A/C]AGAGCAAAGGATAGG | 75770 |
rs36401006 | snp | A/G | 0.260355 | 0.249785 | intron-variant | Brsk2 | Mm_Celera | 7:141959233 | TAGTTTGCAGAGAAA[A/G]CCTTTGGCAAGTCTC | 75770 |
rs36410460 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141980393 | GGTTGTGAATGGGTC[C/T]TTTGTGGAGGAGGGA | 75770 |
rs36414844 | snp | C/T | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141995171 | TCTGTTTTTTAGAAC[C/T]ACTTGTCTGCTTCAA | 75770 |
rs36425000 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Brsk2 | Mm_Celera | 7:141967427 | CTCTCCCGGCTCTAG[C/T]CTACTACCTTCAGAT | 75770 |
rs36430365 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141999884 | GCAGTAGTGGGAAAC[C/G]GAGGACAAGGAATGA | 75770 |
rs36435580 | snp | A/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141994971 | TATGGCTCACACCAT[A/G]TATTCTGTGTACCCA | 75770 |
rs36470806 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brsk2 | Mm_Celera | 7:141959553 | ACTGTCTATGGGCTA[A/G]TGGAAACGTATGCAC | 75770 |
rs36473734 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Brsk2 | Mm_Celera | 7:141971252 | CCCTCAGAACCCTGC[C/T]TTCCAAGGAGGTAAT | 75770 |
rs36476997 | snp | A/C | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141956005 | GTGGGAAGACATAGC[A/C]ACCTTCTCTGGGTGC | 75770 |
rs36497868 | snp | A/G | 0.35503 | 0.226867 | intron-variant | Brsk2 | Mm_Celera | 7:141956084 | CCCTTGTGGTTCTGG[A/G]ATGGCTAGAAGAGGG | 75770 |
rs36500676 | snp | G/T | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141957335 | ATCTCCAGTTTGAGA[G/T]ACCAGACTACAATAG | 75770 |
rs36501153 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141985070 | TGGTGGCCTGTGGCT[A/G]GAGAGCACTAAAGCT | 75770 |
rs36501624 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141973415 | TCCTCAAAAGCCGCA[A/G]AGGAGGCTGCTGCCA | 75770 |
rs36507887 | snp | G/T | 0.408163 | 0.193609 | intron-variant | Brsk2 | Mm_Celera | 7:141973098 | GGGAGCCACTGCCCC[G/T]TCACACACCCACAGT | 75770 |
rs36517408 | snp | A/C | 0.32 | 0.24 | synonymous-codon | Brsk2 | Mm_Celera | 7:141993297 | CCTGGGCTCACCTCG[A/C]TTCCACCGCCGGAAA | 75770 |
rs36521355 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141962651 | CTGTGAAGGTCTGAA[C/T]TCCCATGTCTGCCTG | 75770 |
rs36525856 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Brsk2 | Mm_Celera | 7:141983293 | GATCTGGAGTCTAGG[A/G]CTAGTAGTACTTGTT | 75770 |
rs36535333 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141999760 | CTGCTTGGAAGAAAG[C/T]GAGCAAGCAGGGCCA | 75770 |
rs36542617 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141984258 | CCTAGCTGCCTGGTG[C/T]GAAAGCCACTAGGAG | 75770 |
rs36543749 | snp | C/T | 0.375 | 0.216506 | intron-variant | Brsk2 | Mm_Celera | 7:141960058 | TCTTTCCTGTCACCC[C/T]CTCAGGCTAACTAGG | 75770 |
rs36547560 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141985224 | TTGAGCCTTCTCTCC[C/T]GGGTCTAAGCAGAGC | 75770 |
rs36557192 | snp | G/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141980236 | TTCATTTTTGGCCAA[G/T]TTGTATAATACTGTC | 75770 |
rs36557902 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141990574 | TCCAGGGGAAGAGCT[A/G]GCCTGGGCAGCTATA | 75770 |
rs36582059 | snp | C/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141989732 | CCAACTTTCTAGCCA[C/G]CCATGGCTCACAATC | 75770 |
rs36586259 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141969106 | ACTTAGGTCCTGCTA[A/T]ACCAGGTAACAGTGG | 75770 |
rs36589676 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141991456 | TAGTGTGGTTAGTGG[C/T]GGGCAGGCCAGGGCA | 75770 |
rs36596550 | snp | G/T | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141994777 | TAGAGCCATAGCCGG[G/T]AAAGGAGAGGTATCT | 75770 |
rs36602316 | snp | A/G | 0.408163 | 0.193609 | intron-variant | Brsk2 | Mm_Celera | 7:141986490 | CCAGCTGTTGGGAGG[A/G]ATAGTATCTGCTTAG | 75770 |
rs36602609 | snp | A/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141968796 | CACTCCTGGCCAAAA[A/G]TGACATCCTCTCTGA | 75770 |
rs36625032 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141975651 | GGGTGGAGGACAGGT[A/G]TTATTTAGAAAGTCA | 75770 |
rs36625593 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141988497 | GCCAGGGCAGTACCA[G/T]GTTCTTAGCCTACTA | 75770 |
rs36643419 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141990964 | TACTTGGCTTCCCTC[A/G]GGGCTGGAGTCATCT | 75770 |
rs36646903 | snp | A/C | 0.244898 | 0.249948 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141991616 | AGCTGGATGGAAGGC[A/C]TTGTCTCTGACCTGT | 75770 |
rs36649485 | snp | A/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141987735 | TGACTGCTGCTGGGT[A/G]CCCTGTCGTCCACAG | 75770 |
rs36652650 | snp | G/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141991677 | TAACGGACACATAGG[G/T]GTAGTACCTGCTCCC | 75770 |
rs36655677 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Brsk2 | Mm_Celera | 7:141994490 | CAGACACCTAAGCTC[A/G]CCATTAACTGCCCTG | 75770 |
rs36664852 | snp | G/T | 0.142012 | 0.225474 | intron-variant | Brsk2 | Mm_Celera | 7:141988107 | TGGCACCTCTCACCT[G/T]CTGCAGGGAGAATCA | 75770 |
rs36671116 | snp | A/G | 0.391111 | 0.206368 | utr-variant-3-prime | Brsk2 | Mm_Celera | 7:142002612 | AGAGGCTAGCCCACT[A/G]TCCACCACCTCTGCC | 75770 |
rs36674130 | snp | A/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141972053 | CTTACCTGTGGCCCC[A/G]CCTTAGCTCTGATCC | 75770 |
rs36674815 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Brsk2 | Mm_Celera | 7:141981836 | TTGACCCTGTTAGCC[G/T]GGAGAACAGGCCCAC | 75770 |
rs36676392 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Brsk2 | Mm_Celera | 7:141969025 | AATATGGAGTCTTCA[C/T]ATTTGATGTTTACCA | 75770 |
rs36679922 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141968451 | TGGGTCTGGGCTGAG[A/G]CATGATTTTCATAGG | 75770 |
rs36681141 | snp | C/T | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141984662 | TCAAGGGCAGGAGGA[C/T]ACAGCATCCCTGTCA | 75770 |
rs36690853 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141973032 | ATGGGGCCACCTCCT[A/G]CCAAGCCCACACAGG | 75770 |
rs36695608 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141989173 | TTCAGAGCCCCTTGC[C/T]TATCAGGCTTGTCCC | 75770 |
rs36698925 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141987491 | AACGCCTGCTTTGCC[C/T]GTTGCTGTGGCCTGC | 75770 |
rs36703246 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141984755 | GACTGCCCCACTGAC[A/G]GGAGTTTGAAAAAGG | 75770 |
rs36703681 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Brsk2 | Mm_Celera | 7:141990135 | CTGGTGCTGAGTCTA[G/T]ACATCTCTAAGCTTG | 75770 |
rs36709882 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Brsk2 | Mm_Celera | 7:141966927 | AGGGAGAGTAGTCAC[C/T]TCAGTCAATACAAGG | 75770 |
rs36715964 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141959815 | TACTCACTCCTGGGT[A/G]TCCCTTGTTTCATAG | 75770 |
rs36728647 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141965186 | TGAAGACTGGGTAGG[C/T]TCTCCTGATCGTCTG | 75770 |
rs36728738 | snp | A/G | 0.197531 | 0.244432 | intron-variant | Brsk2 | GRCm38.p3 | 7:141966678 | CCAAGTGCTGTGGGA[A/G]GTGAGGCCTTGGGTC | 75770 |
rs36729784 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141986169 | TGGTGGAGTCTCAAG[C/T]GTCCATCTCTGGCAC | 75770 |
rs36750790 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141978619 | AGGGAGGGGTCTAGG[C/T]GGCTCCCTGCACTTT | 75770 |
rs36751994 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon | Brsk2 | Mm_Celera | 7:141996910 | CAAGAAATCGTGGTT[C/T]GGGAACTTCATCAAC | 75770 |
rs36753334 | snp | A/T | 0.277778 | 0.248452 | intron-variant | Brsk2 | Mm_Celera | 7:141967617 | TAGACCACCTCAAGC[A/T]GCTATGAGTTCCTAT | 75770 |
rs36755846 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Brsk2 | Mm_Celera | 7:141961533 | GAGGAAGAGGTGGCT[A/G]AGGCAGACTAATGCC | 75770 |
rs36758752 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Brsk2, Mir3104 | Mm_Celera | 7:141992045 | AGTGTGGAGGAGCCC[C/T]AGGGACCCTGGATAC | 75770 |
rs36778027 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141980985 | TCCATGAGCCATTCC[A/G]ATCAGTGAGCAAGGT | 75770 |
rs36782657 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141968975 | ACCTTTCAGTGGGAG[A/G]TGAGATGAACAAGTT | 75770 |
rs36790473 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141968744 | TGTGGCCTCCTTACC[C/T]TCACCTGACTGGCCT | 75770 |
rs36806773 | snp | A/G | 0.32 | 0.24 | intron-variant | Brsk2 | Mm_Celera | 7:141979075 | GGAGTATGTGTGTAC[A/G]TCCATGAGAGGGTGA | 75770 |
rs36809064 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Brsk2 | Mm_Celera | 7:141986868 | TCAATGTGAGCCTCC[A/C]AGCTCCATCAACTAT | 75770 |
rs36811147 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Brsk2 | Mm_Celera | 7:141964326 | CCTTTCTGAGTCCTG[A/G]CTTTAGGAGCTTGGA | 75770 |
rs36827355 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Brsk2 | Mm_Celera | 7:141955072 | ATCACTAAGGGTGGT[A/G]CAAGTTGCTAGGAAG | 75770 |
rs36833662 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brsk2 | Mm_Celera | 7:141979830 | TGACCAAGTGCAGAT[A/G]GACTCGTGTCTTAGT | 75770 |
rs36852380 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Brsk2 | Mm_Celera | 7:141967764 | ATATTACCTGCTTCT[A/G]TGAAAGGTACCAGGT | 75770 |