SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs30358386 | snp | G/T | 0.32 | 0.24 | intron-variant | Fxn | Mm_Celera | 19:24272854 | CTCACCTTTCATTTA[G/T]TTCTTTTTTTTTTTT | 14297 |
rs30367581 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fxn | Mm_Celera | 19:24274371 | TTCAGGCCCACTCTC[A/G]GGAATATGCACAACA | 14297 |
rs30371474 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24271768 | CCCGCCCCCCCCCCC[C/T]TTTGACAGCCATCTG | 14297 |
rs30403164 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24263898 | TAAAAGTAGTTTTCT[A/T]TATTGAAAATTAAAG | 14297 |
rs30403170 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24273754 | TCGCCAGAGGCAGTC[A/G]CATCTGCCAAGTCTT | 14297 |
rs30444587 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24262211 | TATCTATTTATCTAT[C/T]TATCTACTTTTGTGT | 14297 |
rs30453567 | snp | G/T | 0.32 | 0.24 | intron-variant | Fxn | Mm_Celera | 19:24271688 | TGTCATGATAAACCA[G/T]GTACCTTCACATACA | 14297 |
rs30500468 | snp | C/T | 0.32 | 0.24 | intron-variant | Fxn | Mm_Celera | 19:24263499 | GCTTGCTTCCCCTGG[C/T]TTGCTCAGCCTGCTC | 14297 |
rs30624176 | snp | C/G | 0.336735 | 0.234472 | intron-variant | Fxn | Mm_Celera | 19:24263913 | TTATTGAAAATTAAA[C/G]CTGTGAAATTGAGAG | 14297 |
rs30720506 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fxn | Mm_Celera | 19:24274385 | CAGGAATATGCACAA[C/T]AGAAACTCCCAGGGT | 14297 |
rs30819204 | snp | A/T | 0.32 | 0.24 | intron-variant | Fxn | Mm_Celera | 19:24271680 | ATGGGAGATGTCATG[A/T]TAAACCATGTACCTT | 14297 |
rs30905301 | snp | A/T | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24274025 | CTTTTGTTACTAAAT[A/T]TTTGTTGGTCAAGAC | 14297 |
rs30913131 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Fxn | Mm_Celera | 19:24262465 | ACCCTTCAATTTGTA[A/G]CACTCTTCTGTTTCA | 14297 |
rs30949074 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24271884 | TCTGCCCGGATTGGG[A/G]GTGTGGAGGAGGGGA | 14297 |
rs30980128 | snp | C/T | 0.32 | 0.24 | intron-variant | Fxn | Mm_Celera | 19:24263606 | ATTGAGAAAATGCCT[C/T]ACAGCTGGATCTCAT | 14297 |
rs30996611 | snp | C/T | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24273890 | GGATTTACAATTCTC[C/T]TGCCTCAGTTTCCCA | 14297 |
rs31055219 | snp | A/G | 0.32 | 0.24 | intron-variant | Fxn | Mm_Celera | 19:24263841 | TTTCTTGCCTTTATC[A/G]CTCAAGTGTTGGGAT | 14297 |
rs31057967 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Fxn | Mm_Celera | 19:24272993 | GCTGGGATTAAAGGC[C/G]TGCACCACCACTGCC | 14297 |
rs31061692 | snp | A/C/T | 0.444444 | 0.157135 | intron-variant | Fxn | GRCm38.p3 | 19:24274254 | GAAAGGCACAGGAGG[A/C/T]GGGGCAAGCAGGGCT | 14297 |
rs31131408 | snp | A/G | 0.32 | 0.24 | intron-variant | Fxn | Mm_Celera | 19:24263640 | GGCATTTCCTCAAGG[A/G]AGGCTCCTTTCTCTG | 14297 |
rs31188062 | snp | A/G | 0.375 | 0.216506 | intron-variant | Fxn | Mm_Celera | 19:24272635 | AGTCCTTCCTGCTCC[A/G]TCAGCCACCTTGATT | 14297 |
rs31288001 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Fxn | Mm_Celera | 19:24274330 | CTGTGGAACATGCTC[A/C]CAGGCTGTGGCCTTT | 14297 |
rs33888448 | snp | C/T | 0.5 | 0 | intron-variant | Fxn | Mm_Celera | 19:24279612 | CCACAGCCTACTCCA[C/T]CTTTGTCCATAGCTC | 14297 |
rs45688048 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Fxn | Mm_Celera | 19:24267003 | TCTGGCAAAAGTATC[A/T]TTTTCAAAGGCAAGC | 14297 |
rs45689784 | snp | C/T | 0.5 | 0 | intron-variant | Fxn | Mm_Celera | 19:24270274 | CCACACCAGGGACAG[C/T]TCTCCTAACCACTGC | 14297 |
rs45720778 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fxn | GRCm38.p3 | 19:24268472 | CCAGACCCTTCCCAG[A/G]CATCCAGCGAGTGCT | 14297 |
rs45736795 | snp | C/T | | | upstream-variant-2KB | Fxn | Mm_Celera | 19:24282025 | AGTTAGAACCCTGGC[C/T]TCCTGATTTCTGGTC | 14297 |
rs45762771 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24265542 | TCTCTAGCACCTAAA[A/G]TTACAGGTTTTAAAT | 14297 |
rs45777172 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fxn | Mm_Celera | 19:24267123 | AACATCCTGATGCCT[C/G]AGTTGCATAGCAACC | 14297 |
rs45789583 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24278992 | GCTGAAGAGACTGAA[C/T]ATCTGCTCACTCCGT | 14297 |
rs45824005 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24275920 | TAAATACAGTGGTTG[A/G]TCTGATAGGCTGTGA | 14297 |
rs45834265 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Fxn | Mm_Celera | 19:24264791 | TCACATGAAAGCAAA[A/G]CAAAACCAGGAGAAA | 14297 |
rs45840136 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Fxn | Mm_Celera | 19:24264755 | AAGAGCAGAAACCTC[C/T]CTGAACACAAAGTAC | 14297 |
rs45843582 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24278834 | CCTGTGCCACCACTG[C/T]CCACCTGAGTGAGGT | 14297 |
rs45848691 | snp | G/T | | | intron-variant | Fxn | Mm_Celera | 19:24275727 | AGGAATATAATGCAT[G/T]AAGCCTTCCTTCTGT | 14297 |
rs45851660 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fxn | Mm_Celera | 19:24264063 | GAGTGACTTCCTGGG[A/G]TCATTGCGATGTGTC | 14297 |
rs45864879 | snp | C/G | 0.231111 | 0.249285 | upstream-variant-2KB | Fxn | Mm_Celera | 19:24282539 | CCAGTGATAGCTATT[C/G]CGGTCGGAAGTGATG | 14297 |
rs45871438 | snp | A/T | | | intron-variant | Fxn | Mm_Celera | 19:24276020 | CAGGACAGCTGGAAT[A/T]GTCTTTTTGTTTTTG | 14297 |
rs45890726 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24269973 | CTCTCTACCCAATTC[C/T]ACAGTTTTCTGCTGC | 14297 |
rs45938444 | snp | A/G | 0.497778 | 0.0332592 | downstream-variant-500B | Fxn | Mm_Celera | 19:24261137 | TCTCAGGTCCATGTC[A/G]TAGCTGCCAACTGTG | 14297 |
rs45938846 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Fxn | Mm_Celera | 19:24267082 | GGGCCAGGCTCTGAA[A/C]AGTTCCTTCTGCTTC | 14297 |
rs45983388 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fxn | Mm_Celera | 19:24262720 | TGGTCTGTCTCACTG[C/T]AGGCCCAAAGGCAAC | 14297 |
rs46001043 | snp | C/G/T | | | upstream-variant-2KB | Fxn | GRCm38.p3 | 19:24280924 | TCTAACAGCTAGCTT[C/G/T]AACTGCCCGATCATC | 14297 |
rs46034072 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fxn | Mm_Celera | 19:24264284 | GTAACTTGTCTCAGG[C/T]ATTCAGGGTAGCGAT | 14297 |
rs46037513 | snp | A/C | | | intron-variant | Fxn | Mm_Celera | 19:24275721 | GGATGAAGGAATATA[A/C]TGCATTAAGCCTTCC | 14297 |
rs46047300 | snp | G/T | | | intron-variant | Fxn | Mm_Celera | 19:24275933 | TGGTCTGATAGGCTG[G/T]GATGGACATTTCGAG | 14297 |
rs46082527 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fxn | Mm_Celera | 19:24270696 | TGATATTATGTTTGT[A/G]GATGGATGAACCCAT | 14297 |
rs46102301 | snp | G/T | 0.375 | 0.216506 | intron-variant | Fxn | GRCm38.p3 | 19:24268788 | TCAGGAGACTTGGAC[G/T]GATTCTCACAGCACA | 14297 |
rs46120784 | snp | A/G | 0.497041 | 0.0383476 | intron-variant | Fxn | Mm_Celera | 19:24270465 | GTCCCCTCTTGCTCC[A/G]GGACTGTGCAGGTGG | 14297 |
rs46190450 | snp | C/G | 0.231111 | 0.249285 | intron-variant | Fxn | GRCm38.p3 | 19:24268685 | CACTTTAAAGGGGCC[C/G]GGTATTGCTTCTGGA | 14297 |
rs46199571 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24278143 | TTTTCTCCCTCATGG[A/G]GTTATGAGGGAAGAA | 14297 |
rs46217464 | snp | A/G | | | upstream-variant-2KB | Fxn | Mm_Celera | 19:24282006 | TCCCCCCTGATTGAA[A/G]GGGAGTTAGAACCCT | 14297 |
rs46267646 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Fxn | Mm_Celera | 19:24282576 | ATATTCCCAAAACAA[C/T]GACTTCCACGATGGG | 14297 |
rs46293161 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24266824 | TGGATAGCCCTGGCT[A/G]TCCTGGAACGCACTA | 14297 |
rs46308720 | snp | C/G/T | | | intron-variant | Fxn | GRCm38.p3 | 19:24270836 | ATTAGACGCTTCCCC[C/G/T]AGGACTTCCAGCCAT | 14297 |
rs46319651 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24279083 | CGCTTTTGGCCAGTC[C/T]GCCGCTTTCAAAGTG | 14297 |
rs46347456 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Fxn | Mm_Celera | 19:24263042 | GCTAATTTTGTACCA[C/G]GGATGTGCTGATCAA | 14297 |
rs46357933 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24278539 | ATGCGTATGCATAAT[C/T]CTGTTTGTGCATGTC | 14297 |
rs46407316 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fxn | Mm_Celera | 19:24264012 | AAAGCATTTGGGATG[C/T]GGTTTTATACTACCT | 14297 |
rs46418998 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24273262 | CTTTTTGATACATAT[A/G]CAGCTAGAGTCAAGA | 14297 |
rs46512118 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24278065 | CCAGCTGCCATGTGC[C/T]CGAGAGTCGTCTCTC | 14297 |
rs46572586 | snp | C/T | | | upstream-variant-2KB | Fxn | Mm_Celera | 19:24282039 | CTTCCTGATTTCTGG[C/T]CCGAGGGCTCTTACA | 14297 |
rs46679169 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fxn | Mm_Celera | 19:24266212 | CAGTGCATCCTGCTG[C/T]TCCTTCAACTGCAGG | 14297 |
rs46696692 | snp | A/G | 0.336735 | 0.234472 | upstream-variant-2KB | Fxn | Mm_Celera | 19:24282571 | TGCACATATTCCCAA[A/G]ACAATGACTTCCACG | 14297 |
rs46737613 | snp | C/T | | | downstream-variant-500B | Fxn | Mm_Celera | 19:24260953 | AGCTCAAATTTTCTT[C/T]GTATTTTCCTTAGAC | 14297 |
rs46744925 | snp | A/C | 0.42 | 0.183303 | intron-variant | Fxn | GRCm38.p3 | 19:24268390 | AAAGGAGAAGAAAGT[A/C]ATCCATGCCCTTTCT | 14297 |
rs46786575 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24270558 | GAACTGCCTCTGCAT[C/T]GACTTGTATGTCAGG | 14297 |
rs46789606 | snp | A/C | | | upstream-variant-2KB | Fxn | Mm_Celera | 19:24281993 | CATATTAAGTGACTC[A/C]CCCCTGATTGAAGGG | 14297 |
rs46789899 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fxn | Mm_Celera | 19:24266184 | TCCTTAGTTCTGAGA[C/T]AGGGTCTGACTGCAG | 14297 |
rs46805536 | snp | G/T | 0.21875 | 0.248039 | intron-variant | Fxn | Mm_Celera | 19:24269987 | CCACAGTTTTCTGCT[G/T]CTAGCTATAGGCTAA | 14297 |
rs46820594 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Fxn | Mm_Celera | 19:24261707 | GGGAGCAAATGACAT[A/G]ATCCTAACAAATGTC | 14297 |
rs46940339 | snp | C/T | 0.497778 | 0.0332592 | downstream-variant-500B | Fxn | Mm_Celera | 19:24261169 | AAATGACCCCCACTA[C/T]GAAGGCACAGAGTTA | 14297 |
rs46945601 | snp | A/C | | | intron-variant | Fxn | Mm_Celera | 19:24274661 | AAATAAACAACCATA[A/C]AAGCCAATTCAAGCA | 14297 |
rs46991019 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fxn | Mm_Celera | 19:24266195 | GAGACAGGGTCTGAC[C/T]GCAGTGCATCCTGCT | 14297 |
rs47030203 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Fxn | GRCm38.p3 | 19:24268062 | CAGCCACCACGAGTG[A/G]ATGAATCGTAATAGC | 14297 |
rs47042553 | snp | C/T | | | intron-variant | Fxn | Mm_Celera | 19:24265487 | GATTGACCTCAGGAC[C/T]TTTGGAAGTGCAGTC | 14297 |
rs47043346 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24279676 | TTGGCATCTATCACG[A/G]CCCTCTCCGGAAAGC | 14297 |
rs47094970 | snp | A/C | 0.473373 | 0.11227 | intron-variant | Fxn | Mm_Celera | 19:24264862 | CAGGTAGAGTTGGAA[A/C]AACTCAAGACCCCTC | 14297 |
rs47135977 | snp | C/T | | | intron-variant | Fxn | GRCm38.p3 | 19:24280233 | TTAATTACGGAAACT[C/T]GTCTTTTCCCATCCC | 14297 |
rs47180672 | snp | A/T | | | intron-variant | Fxn | Mm_Celera | 19:24274519 | ACTGAGCTCCAGCTA[A/T]GGACCACCACCTAAC | 14297 |
rs47199569 | snp | A/T | | | intron-variant | Fxn | Mm_Celera | 19:24277744 | CTTTCTGCTGCCTGC[A/T]GCCTCTCAGCTGATC | 14297 |
rs47227774 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Fxn | Mm_Celera | 19:24270399 | GCAGAAAGCCACCCA[C/T]GAGAGACCTGACTTG | 14297 |
rs47290471 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fxn | Mm_Celera | 19:24270548 | CTCCTGCTTTGAACT[A/G]CCTCTGCATCGACTT | 14297 |
rs47294422 | snp | A/G | 0.459184 | 0.136902 | intron-variant | Fxn | Mm_Celera | 19:24264505 | CCCCACACTAGAAGA[A/G]TGGGGACACAGCTTA | 14297 |
rs47347765 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Fxn | GRCm38.p3 | 19:24267795 | ACCAAACAAACTTTA[A/G]TGCTCAAAAACAGGA | 14297 |
rs47359538 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fxn | GRCm38.p3 | 19:24265361 | TTTTTAAATTAACTG[C/T]TTTTATGTTGTTTTG | 14297 |
rs47366865 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Fxn | Mm_Celera | 19:24264604 | GAGGAGACTGAGGTG[C/T]GGTGGGAAGGCAGGG | 14297 |
rs47391407 | snp | A/T | | | intron-variant | Fxn | Mm_Celera | 19:24274582 | GTGACAGATGTCACA[A/T]ATGACAGTGATGGGA | 14297 |
rs47419673 | snp | C/T | 0.391111 | 0.206368 | intron-variant | Fxn | Mm_Celera | 19:24264311 | CGATGTGAAGCTGAC[C/T]AATACACGGTACTGC | 14297 |
rs47422649 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24279349 | AAGAAAGTGTTTGAG[A/G]AAGCATGGGTTACAG | 14297 |
rs47497867 | snp | C/T | 0.497778 | 0.0332592 | intron-variant | Fxn | Mm_Celera | 19:24264556 | TCCCAGCGTGGTGAC[C/T]GCATTGTTAGATCTC | 14297 |
rs47519412 | snp | G/T | | | intron-variant | Fxn | Mm_Celera | 19:24279369 | ATGGGTTACAGGTTC[G/T]GCCCTTCAAACCCTA | 14297 |
rs47531744 | snp | C/T | 0.48 | 0.0979796 | upstream-variant-2KB | Fxn | Mm_Celera | 19:24281698 | CTGAGCTTCAAGAGT[C/T]AAGAGACAGTGTCAG | 14297 |
rs47568633 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Fxn | GRCm38.p3 | 19:24268480 | TTCCCAGACATCCAG[C/T]GAGTGCTCCAGACTC | 14297 |
rs47679417 | snp | A/G | 0.124444 | 0.216185 | synonymous-codon | Fxn | Mm_Celera | 19:24262053 | ATAGCGCTTGGGGCC[A/G]CTGCGAGACAAAACA | 14297 |
rs47735543 | snp | A/T | 0.48 | 0.0979796 | upstream-variant-2KB | Fxn | GRCm38.p3 | 19:24281773 | CAGCGGTCAGCAGCA[A/T]AGCGTTTAAGAACAT | 14297 |
rs47792820 | snp | A/C | | | intron-variant | Fxn | Mm_Celera | 19:24265478 | GTTGCTGGGGATTGA[A/C]CTCAGGACCTTTGGA | 14297 |
rs47816127 | snp | A/T | 0.5 | 0 | upstream-variant-2KB | Fxn | Mm_Celera | 19:24282172 | CAGTGAGGGCTACGC[A/T]ACCGGTCAGCATCAT | 14297 |
rs47838951 | snp | A/G | | | upstream-variant-2KB | Fxn | Mm_Celera | 19:24280984 | GTACCAGGCAGCATG[A/G]ATGGAGGAGGGGCTT | 14297 |
rs47864119 | snp | A/G | | | intron-variant | Fxn | Mm_Celera | 19:24276239 | GCCTCTTTATAAGGC[A/G]ATGGAATGGACAGGA | 14297 |