SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs13468374 | snp | C/G | 0.5 | 0 | utr-variant-3-prime | Brap | GRCm38.p3 | 5:121686424 | ACCAACAGAGGGGCT[C/G]TGTGCCTCTCTTTAG | 72399 |
rs13468375 | snp | A/G | 0.432133 | 0.171253 | utr-variant-3-prime | Brap | GRCm38.p3 | 5:121686488 | ATTGAACAGACTTGA[A/G]GGGACACCATGTTGG | 72399 |
rs29503773 | snp | A/G | 0.375 | 0.216506 | intron-variant | Brap | GRCm38.p3 | 5:121678090 | GAGAAGAGCAGCACT[A/G]GCTGCTCTTGCAGAA | 72399 |
rs29522760 | snp | C/T | 0.475309 | 0.108333 | intron-variant, upstream-variant-2KB | Brap, Acad10 | GRCm38.p3 | 5:121662186 | CAGGAAGCCTGGCCG[C/T]GCTCAAGTACTCTGA | 72399 |
rs29525761 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Brap, Acad10 | GRCm38.p3 | 5:121659953 | ACAGAGTGAGTTCTA[A/G]GACAGCTAGGCGTAC | 72399 |
rs29540961 | snp | C/T | 0.375 | 0.216506 | intron-variant | Brap | GRCm38.p3 | 5:121683110 | TGAGTTAGAGGCCAG[C/T]CTGGTCTACAAAGTG | 72399 |
rs29580214 | snp | A/G | 0.492188 | 0.0620098 | downstream-variant-500B | Brap | GRCm38.p3 | 5:121687296 | GGAAGCTGTTAGTAT[A/G]TTCTTCAGAACAGAG | 72399 |
rs29586932 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | Brap, Acad10 | GRCm38.p3 | 5:121658568 | TTTCTCCTTGTCAAT[C/T]AGAATGAGGTTAGAC | 72399 |
rs29634629 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Brap | Mm_Celera | 5:121674811 | ACCCCCCAAAAAAAT[A/T]TAAAAAAAATAAAAA | 72399 |
rs29672360 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Brap | GRCm38.p3 | 5:121669415 | CTGGCAGAGGAAGCT[C/T]TGATAATGATCCTCT | 72399 |
rs29678051 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Brap | Mm_Celera | 5:121674857 | GTGGAGAAATGGCCC[A/C]CTGACTGCTCTTCTA | 72399 |
rs29679302 | snp | A/T | 0.5 | 0 | intron-variant | Brap | Mm_Celera | 5:121677743 | GGCAGGAGGCATTGG[A/T]GCTTCCTTCTTGCCT | 72399 |
rs29771059 | snp | G/T | 0.5 | 0 | intron-variant | Brap | Mm_Celera | 5:121666777 | TTTTTTTTTTTTGTT[G/T]TTTTTTTTTTAATTC | 72399 |
rs29776768 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Brap, Acad10 | GRCm38.p3 | 5:121659587 | TCCTCAGTGTGTGTG[C/T]TCACTATAGCACCTG | 72399 |
rs29779858 | snp | A/G | 0.5 | 0 | intron-variant | Brap | Mm_Celera | 5:121677736 | AAGGAGAGGCAGGAG[A/G]CATTGGTGCTTCCTT | 72399 |
rs33107038 | snp | C/T | 0.5 | 0 | intron-variant | Brap | Mm_Celera | 5:121683588 | GTAGAGGCAAGAGGA[C/T]TGTTTAATCTCAGAA | 72399 |
rs33152707 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Brap, Acad10 | GRCm38.p3 | 5:121659519 | ATGTGTGTGTGTATT[C/T]TAGACACTGAACCCA | 72399 |
rs33158460 | snp | A/T | 0.5 | 0 | intron-variant | Brap | Mm_Celera | 5:121669013 | TGGCAAGTGCCTTTA[A/T]TTTTTGCATCATCTT | 72399 |
rs33198394 | snp | A/G | 0.465374 | 0.126941 | intron-variant | Brap | GRCm38.p3 | 5:121667257 | TTGAACTTTGACCAT[A/G]TTAGTCAGGTGGTGG | 72399 |
rs33216975 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Brap | Mm_Celera | 5:121674812 | CCCCCCAAAAAAATT[A/T]AAAAAAAATAAAAAA | 72399 |
rs33247918 | snp | A/T | 0.5 | 0 | intron-variant | Brap | GRCm38.p3 | 5:121673168 | TGCTACCATGCTTAG[A/T]TTTTTGTTTTGTTTG | 72399 |
rs33313625 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Brap | GRCm38.p3 | 5:121681107 | TCAGGAGCTCACTGG[C/T]ATTGAACTCAGGAGG | 72399 |
rs33313629 | snp | C/T | 0.5 | 0 | intron-variant | Brap | Mm_Celera | 5:121667196 | CAGCTTTGGATTTAC[C/T]CAAGCTTTTTTTTTC | 72399 |
rs33320977 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Brap | GRCm38.p3 | 5:121662689 | CCCGGGGAAGCCTGC[C/T]GCCCCGTCCCTGCCC | 72399 |
rs33361581 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Brap | GRCm38.p3 | 5:121662579 | CCCTGTTTTAAGAGA[A/G]TAATACAGGAGAAAC | 72399 |
rs33373505 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Brap | GRCm38.p3 | 5:121683972 | TCAAGGAACCTTGGG[C/T]GCTGCAGAGAAGAGG | 72399 |
rs33462165 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Brap | GRCm38.p3 | 5:121664567 | GAGGACCTGGGTTCA[G/T]TTTCCAGCACCCACA | 72399 |
rs33486340 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Brap, Acad10 | GRCm38.p3 | 5:121660538 | GGGGCCTCGCCCCTT[C/T]CCGCGTGCGCGTGCG | 72399 |
rs33499228 | snp | A/G | 0.487535 | 0.077957 | intron-variant | Brap | GRCm38.p3 | 5:121675490 | GCTCTGCAAAGCTGG[A/G]ATCTCAGAAGTGAAG | 72399 |
rs33499765 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Brap | GRCm38.p3 | 5:121677492 | GAAGGTCTCTTCTGG[C/T]TTCTACAGGTACTGT | 72399 |
rs33513804 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB, intron-variant | Brap, Acad10 | GRCm38.p3 | 5:121659686 | TGGAAGTAACCCTGG[C/T]ACTGATGAGGTGGAA | 72399 |
rs33570937 | snp | A/C | 0.465374 | 0.126941 | intron-variant | Brap | GRCm38.p3 | 5:121675822 | TTTAAAAACCCTTTT[A/C]TGGCCTCTGTAGGCA | 72399 |
rs33576888 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Brap | GRCm38.p3 | 5:121663641 | GTTCTGAGTGTTGTG[C/T]GTTTGACAGTGTAGA | 72399 |
rs33601430 | snp | C/T | 0.475309 | 0.108333 | utr-variant-3-prime | Brap | GRCm38.p3 | 5:121686734 | TGCTGTAGCATTTCC[C/T]AAAACCCCACCTGTG | 72399 |
rs33622457 | snp | G/T | 0.48 | 0.0979796 | intron-variant | Brap | Mm_Celera | 5:121672581 | AACATACGAAAAAAT[G/T]TTATATCTCAGTTTT | 72399 |
rs33736547 | snp | C/T | 0.5 | 0 | intron-variant | Brap | GRCm38.p3 | 5:121676973 | CTCCTCTTCCCTCTC[C/T]TTTCCTCTCTTCCTC | 72399 |
rs45673536 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Brap | Mm_Celera | 5:121684439 | GGAGCTCAGGCTCAG[C/T]GACCTCCTGAAGGAG | 72399 |
rs45708602 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121678985 | TTTTAAAAGACTGAG[A/T]TGCCCACCAATCAGT | 72399 |
rs45720080 | snp | C/T | 0.444444 | 0.157135 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Brap, Acad10 | GRCm38.p3 | 5:121661132 | GACTTCCTTAGTGGG[C/T]CATGCAGCTTCGGCT | 72399 |
rs45732474 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121669203 | TGCTTATGCAGGACT[A/G]ACTGGGATTCTGGTC | 72399 |
rs45809985 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121667533 | GGGTGAAGGGAACTC[A/G]TGACACAGACTTCCT | 72399 |
rs45897598 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Brap | Mm_Celera | 5:121677853 | ACTTGGTGGCACTTC[A/G]GTCACTTACAACTGT | 72399 |
rs45898286 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121664905 | CATTTAGGGCTTGCC[A/G]TAAAGTGCACTGCAG | 72399 |
rs45977689 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121669065 | TTTCTTTGGAGGTTC[A/G]GGAAAAGTCATAGAT | 72399 |
rs45981977 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Brap | Mm_Celera | 5:121681129 | CTCAGGAGGTATGCA[C/T]GCTTCCCACATGCTA | 72399 |
rs46099035 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121684234 | TTCTCTCAATTTCTC[A/G]TGATTTTTGTTGTTG | 72399 |
rs46279610 | snp | A/T | 0.132653 | 0.220748 | utr-variant-3-prime | Brap | Mm_Celera | 5:121687200 | TAAAAATGTTCCAGG[A/T]AAACAAAAATCAAGA | 72399 |
rs46283749 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121683529 | GATTACCTTAAATGT[A/G]ACATACATGGTGGCC | 72399 |
rs46441674 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121669379 | AACAAACAGTAAAAA[C/T]ACACTCAGCTCTGTA | 72399 |
rs46509345 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121666270 | TTTTGGTGAAGATTG[A/G]TCCCAGCACCTCACA | 72399 |
rs46514473 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Brap | Mm_Celera | 5:121667496 | TTTGTTCTTGCCACT[C/T]GAATGGGTTACTAAG | 72399 |
rs46638280 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Brap | Mm_Celera | 5:121680646 | AAAAAGAAAAGTTTA[A/G]CCAGGAAAACAAACC | 72399 |
rs46644105 | snp | C/T | 0.132653 | 0.220748 | synonymous-codon | Brap | Mm_Celera | 5:121682857 | GCGCATAGAGAAGGA[C/T]ACGGCAGAGGAGGTA | 72399 |
rs46833276 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121671028 | TTCTCCACGTCTATT[A/C]CAATTTATGCCACCA | 72399 |
rs46932897 | snp | C/T | 0.260355 | 0.249785 | utr-variant-3-prime | Brap | Mm_Celera | 5:121686917 | ATCTAGAACGCGTTA[C/T]ACACTGTTACAGTCT | 72399 |
rs46948997 | snp | G/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121671001 | CCTGATCTGGTGTTG[G/T]TTTGCGTTACCTTCT | 72399 |
rs47119885 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Brap | Mm_Celera | 5:121663726 | GCTTGGGAAATAATC[C/T]ATTAACCGTTAGGCA | 72399 |
rs47210522 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121680402 | GGGATTTTCCTTCTG[A/T]GAAGCCATGTGTGCA | 72399 |
rs47309648 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Brap | Mm_Celera | 5:121684922 | GGAAAACCATTTTGT[C/T]TAAGCTGGTGTCACA | 72399 |
rs47340489 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Brap, Acad10 | Mm_Celera | 5:121661664 | CCTGGAGACATTTAT[A/G]CAGTAAAGCCTAGGG | 72399 |
rs47351039 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Brap | Mm_Celera | 5:121686832 | GCAGATCCTCCGGCC[C/T]GAGCCACACAGGCGG | 72399 |
rs47414081 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121664412 | CTCAGTCCCATTGTC[A/G]GAGGTTAGAATTGTT | 72399 |
rs47504995 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Brap | Mm_Celera | 5:121684084 | TGATCCGTCTAATAA[C/T]GTAGTCCCTCCTCTC | 72399 |
rs47638029 | snp | C/T | 0.297521 | 0.245442 | utr-variant-3-prime | Brap | Mm_Celera | 5:121687134 | CTGGGAAGGCTGTGG[C/T]CAGTGGAAGCAGCCG | 72399 |
rs47703023 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Brap | Mm_Celera | 5:121682750 | GTCATACTTGGTGAT[G/T]GCTCTCATCTCCCAC | 72399 |
rs47781925 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Brap | Mm_Celera | 5:121668271 | GTGCCTTTTCCTTCA[C/T]GGTACTTGTTAATCA | 72399 |
rs47809659 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Brap, Acad10 | Mm_Celera | 5:121661943 | ATTGATTGATGTGCC[A/G]AGAAGTGAGAGGAAT | 72399 |
rs48043168 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121664935 | GACACGTGGAAAAGG[A/T]CCCAGGTACCCATAG | 72399 |
rs48171497 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121680390 | GCTTAGCACACTGGG[A/G]TTTTCCTTCTGAGAA | 72399 |
rs48280669 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121683897 | AGTGTGATGTGATTT[A/G]CAGAAGCCTGTGCAG | 72399 |
rs48444890 | snp | G/T | 0.231111 | 0.249285 | intron-variant, utr-variant-5-prime, upstream-variant-2KB | Brap, Acad10 | Mm_Celera | 5:121661077 | GCGAGTTTTAGCCCA[G/T]CCGGGGACCGAGAGG | 72399 |
rs48556709 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121664318 | GGATCCCAGCCATCA[C/T]GTCTGTTTTCAGCAT | 72399 |
rs48603100 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Brap | Mm_Celera | 5:121675129 | GCCTGGCCTACAGGG[A/G]AACTCTGTCTCCAAA | 72399 |
rs48829537 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Brap | Mm_Celera | 5:121662806 | GCCCTGACTTGTCAC[A/C]GAGGAGCCAGTGGTG | 72399 |
rs49079103 | snp | C/T | 0.32 | 0.24 | intron-variant | Brap | Mm_Celera | 5:121684485 | AGGAAGTGAGTGTCC[C/T]TCGGCTCCTAGCAGC | 72399 |
rs49129243 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Brap | Mm_Celera | 5:121665384 | CAAATTCAGATATGG[C/T]TCCTAGGGTGTGGTT | 72399 |
rs49159221 | snp | C/T | 0.32 | 0.24 | intron-variant | Brap | Mm_Celera | 5:121682528 | GTCCTTATTCTTTCT[C/T]TCATATTCATTCTGT | 72399 |
rs49274401 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121680233 | GAAGCTGGAAATGGA[A/G]CAGACTGAGTCAGAG | 72399 |
rs49345537 | snp | C/T | 0.244898 | 0.249948 | utr-variant-3-prime | Brap | Mm_Celera | 5:121686529 | CTAAAAGAGCCTGGG[C/T]AGTTGACAGCTGTGT | 72399 |
rs49371097 | snp | G/T | 0.244898 | 0.249948 | intron-variant | Brap | Mm_Celera | 5:121680014 | CTTTGACCCTTTCAT[G/T]TTGTCATCTGCCCCG | 72399 |
rs49385597 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121671176 | ACACCTTGATCTGCA[C/T]GAGGCATCCTGACAG | 72399 |
rs49585140 | snp | G/T | | | intron-variant | Brap | Mm_Celera | 5:121671295 | TTTGGGTTTTGTTGG[G/T]TTTTTTTTTGTTTTT | 72399 |
rs49643434 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Brap | Mm_Celera | 5:121665252 | CAGGGACTCTACTCC[A/G]AATCAGTACATGGTA | 72399 |
rs49761966 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121680029 | GTTGTCATCTGCCCC[A/G]TGTCATTGCTGGGAA | 72399 |
rs49795535 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121681070 | AAGTATCTCTTCCAT[A/G]TGAATTCTGACTAAG | 72399 |
rs49945235 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121667506 | CCACTCGAATGGGTT[A/G]CTAAGGTTTGTGGGT | 72399 |
rs50106012 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Brap | Mm_Celera | 5:121669239 | AAACATAAAAGCATG[G/T]AGAGCCCAGCTGGCC | 72399 |
rs50115711 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121670963 | AGTTTAGCACTGGAG[C/T]CGTCTTGTTGCTTTA | 72399 |
rs50218752 | snp | A/G | 0.142012 | 0.225474 | intron-variant | Brap | Mm_Celera | 5:121665428 | CCCCAAGGCTATTAG[A/G]AATACAATTACGGGC | 72399 |
rs50535867 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Brap | Mm_Celera | 5:121664297 | CAGTCCTCAGGTAGC[C/T]GTTTTGGATCCCAGC | 72399 |
rs50555984 | snp | A/C | 0.132653 | 0.220748 | intron-variant | Brap | Mm_Celera | 5:121682906 | ATGCCATAGCAAGGC[A/C]GATAGAGAGGGCAAA | 72399 |
rs50641266 | snp | C/T | 0.459184 | 0.136902 | intron-variant, upstream-variant-2KB | Brap, Acad10 | Mm_Celera | 5:121661500 | TGCAGTAGAAGAGTG[C/T]GTTGTGGTCTTTCTT | 72399 |
rs50660525 | snp | G/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Brap, Acad10 | Mm_Celera | 5:121661763 | TGTGGGTTGAGTGCC[G/T]TACTGGACAGGCCTG | 72399 |
rs50661620 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Brap, Acad10 | Mm_Celera | 5:121661449 | GTTCTCGGAAGGATG[A/G]CATCCTGGACACTCT | 72399 |
rs50706150 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Brap | Mm_Celera | 5:121680326 | CTTTGTGAATTGGGG[C/T]TCAGTTACTTAAAGG | 72399 |
rs50748454 | snp | G/T | | | intron-variant | Brap | Mm_Celera | 5:121666918 | AGCTGGCTTCAGTGT[G/T]TGCTTTTTTTTTTAA | 72399 |
rs51089112 | snp | A/C | 0.32 | 0.24 | intron-variant | Brap | Mm_Celera | 5:121681453 | ATCCAGAGACCAATG[A/C]AGCCCTCATTTCCAG | 72399 |
rs51373343 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Brap | Mm_Celera | 5:121682640 | CCGCAGGTGTTTGCG[C/T]TCTAATTTCATGAGG | 72399 |
rs51569071 | snp | C/T | 0.231111 | 0.249285 | utr-variant-5-prime, synonymous-codon, upstream-variant-2KB | Brap, Acad10 | Mm_Celera | 5:121662046 | GAAGACATTGGCTTC[C/T]GCTGTCGCCTGTCTA | 72399 |
rs51616836 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Brap | Mm_Celera | 5:121687138 | GAAGGCTGTGGCCAG[C/T]GGAAGCAGCCGACGG | 72399 |