SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3673888 | snp | C/T | 0.473373 | 0.11227 | intron-variant | Rnf19a | Mm_Celera | 15:36261866 | GAGCTTTCTAGTTCT[C/T]ATTGAAAGCAACATC | 30945 |
rs3674273 | snp | C/T | 0.5 | 0 | intron-variant | Rnf19a | Mm_Celera | 15:36261885 | GAAAGCAACATCAAA[C/T]AAGCCTATCGATTAA | 30945 |
rs3674290 | snp | A/G | 0.5 | 0 | intron-variant | Rnf19a | Mm_Celera | 15:36261895 | TCAAACAAGCCTATC[A/G]ATTAAGTTTTTGTTT | 30945 |
rs3677205 | snp | A/G | 0.492188 | 0.0620098 | intron-variant | Rnf19a | Mm_Celera | 15:36265251 | AGAAAAACAAATTAA[A/G]GTAAGCCAAAAGATA | 30945 |
rs3689314 | snp | A/G | 0.5 | 0 | intron-variant | Rnf19a | Mm_Celera | 15:36262044 | TATCTGCATAACTAC[A/G]AGACTTGAAGAAGCA | 30945 |
rs3690032 | snp | A/G | 0.396694 | 0.202437 | intron-variant | Rnf19a | Mm_Celera | 15:36262163 | GAATTTGTTGAAATA[A/G]TACAAATTAATGGCA | 30945 |
rs3703216 | snp | A/G | 0.48 | 0.0979796 | upstream-variant-2KB | Rnf19a | Mm_Celera | 15:36285507 | GAGGAAAAAAATGCT[A/G]CTTTCTTTTATAAGT | 30945 |
rs31570083 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36243534 | ATAGAAGCAAGGCAG[A/G]CCTACTTTCTACAAT | 30945 |
rs31572668 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36258057 | TCGGTGAAGGTGCAG[C/T]CTCAGTGTCAGGTTG | 30945 |
rs31586520 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36256956 | CCACTTACTCCTAGA[C/T]TGAACATACAAAGTT | 30945 |
rs31587141 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36266684 | ATGGAGAACACACAC[A/G]CCACAAACAGCTAAT | 30945 |
rs31587202 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36257248 | GTAAGGTTTCTATAA[A/G]AGAAACATAAGACAC | 30945 |
rs31598396 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36280307 | CTCTAAAACTTTCTA[C/T]TTCTTGAATATAGAA | 30945 |
rs31633843 | snp | C/T | 0.387812 | 0.208586 | intron-variant | Rnf19a | Mm_Celera | 15:36251509 | AGAACCTTTCTAAAC[C/T]GCACTGTTGTTCAGA | 30945 |
rs31636760 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36258998 | GTGGGACTCTGCATC[C/T]GCCCTTATCAGTTGC | 30945 |
rs31649696 | snp | G/T | 0.465374 | 0.126941 | intron-variant | Rnf19a | Mm_Celera | 15:36256935 | TAAGTAAGGTATGGT[G/T]TTTATCCACTTACTC | 30945 |
rs31667984 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36243717 | AGGGCTAATGCTTCA[A/C]GTTTAAAAACAGCAG | 30945 |
rs31668222 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf19a | Mm_Celera | 15:36285012 | CCAAGAGAACGTGGG[A/G]AAATTGAGATGCCTA | 30945 |
rs31670427 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36273741 | GGCTTAGACCCAGTC[C/T]TTCCAATAGCTACGA | 30945 |
rs31672010 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Rnf19a | Mm_Celera | 15:36239502 | TGAGGGATTGTTCGG[A/G]ATTAAATCATTTGAA | 30945 |
rs31675488 | snp | C/G/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36251145 | GGTTTCTCTTATAGC[C/G/T]CTGGCTATCCTGGGA | 30945 |
rs31684436 | snp | A/C | 0.35503 | 0.226867 | intron-variant | Rnf19a | Mm_Celera | 15:36269327 | ATGTACACATGTACA[A/C]ACATAGACCTCATTA | 30945 |
rs31687222 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36272546 | TAAGATAAGCTGTGT[C/T]TCAATGGTACCTTAC | 30945 |
rs31721268 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rnf19a | Mm_Celera | 15:36246093 | ACATCCAATCATAGT[A/G]TAACAAAGCTATCAG | 30945 |
rs31732001 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36280074 | CAGAGGCCCTGAGTT[C/T]AAATCTCAGCAACCA | 30945 |
rs31735837 | snp | A/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36272848 | AGGAAAGCTAGATTT[A/T]AAAAAAAAATGTCTA | 30945 |
rs31737508 | snp | A/G | 0.497778 | 0.0332592 | intron-variant | Rnf19a | Mm_Celera | 15:36259906 | GGCACCCTGTTTAAG[A/G]CAAGCAAAAGGTGAG | 30945 |
rs31737546 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36272641 | GTGTTCTTATTAAAC[A/G]AGTGTTTCTACATTT | 30945 |
rs31739034 | snp | A/C/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | GRCm38.p3 | 15:36254810 | GCCACTTCATATTCA[A/C/G]CTACGGCACTGTCCA | 30945 |
rs31761450 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36255148 | GGTTTCCATTACCCA[A/T]CTATATTCTCTATCT | 30945 |
rs31763157 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36269099 | GAATGCTAGGTGTGG[C/T]TACTTGACCTATAAT | 30945 |
rs31796969 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36276389 | AGAGGCGGGCCTGTG[C/T]TCGCTCCTGTACTCT | 30945 |
rs31811590 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Rnf19a | Mm_Celera | 15:36260893 | CATCAAAACAAATGA[C/T]TGACAGAAGTAACAA | 30945 |
rs31811751 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36252039 | TATCAACGTTTATAG[A/G]ACAGCAGTAGGGATC | 30945 |
rs31826950 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | GRCm38.p3 | 15:36279052 | TCTCTGTGTAGCCCT[A/G/T]GCTGTCCTGGAACTC | 30945 |
rs31835636 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36267617 | GGATACAAGTTTTGG[C/T]ATTCACCTTCTCTCT | 30945 |
rs31845000 | snp | C/G | 0.42 | 0.183303 | intron-variant | Rnf19a | Mm_Celera | 15:36243248 | GCACAGATCTTCTCT[C/G]CTTGTTTATCAGGGA | 30945 |
rs31850167 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36246375 | TGCAGATAGTCAGGG[C/T]AGGAGTTGGACCTTA | 30945 |
rs31857394 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36243683 | GTGGGTTAATTAAAC[G/T]CAGGGTCTCAGGTCT | 30945 |
rs31859079 | snp | A/G | 0.5 | 0 | intron-variant | Rnf19a | Mm_Celera | 15:36269040 | TCATTAGATAAGCGC[A/G]CTTGCTACACAAGCA | 30945 |
rs31866221 | snp | A/G | 0.444444 | 0.157135 | downstream-variant-500B | Rnf19a, Mir8097 | Mm_Celera | 15:36239619 | GATAAAAAACATGAA[A/G]AAGGAAGCTTTTGCA | 30945 |
rs31879900 | snp | A/C/G | 0.444444 | 0.157135 | intron-variant | Rnf19a | GRCm38.p3 | 15:36251281 | GTATAAGCTCAATAA[A/C/G]TCTTTCCCTCCTTGC | 30945 |
rs31886063 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36259049 | TCTGATGGGAATTAT[A/G]CTTGGGCTCTGGTCC | 30945 |
rs31892205 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36251028 | GGAGCAAGCCAGTAA[A/G]CAGCACCCTTCCATG | 30945 |
rs31900337 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rnf19a | Mm_Celera | 15:36261291 | CAGCGTAAAAGATTG[C/T]GATATCCTTGACTGT | 30945 |
rs31900756 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36258778 | CCCCCACTTCCACTG[C/T]TAGAAATTCCACAAG | 30945 |
rs31902674 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36245673 | ATAGGAGTGACCCCT[C/T]CCTCATGTTCCTGGC | 30945 |
rs31935455 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36246309 | TAGAAACAGGAGTGT[A/G]ACTGTCATCTTTGAG | 30945 |
rs31941958 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36263732 | TTCAACAAGTTCTTT[A/T]AAAAATTTTTTTTAT | 30945 |
rs31950282 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Rnf19a | Mm_Celera | 15:36250264 | CTTGCACATGCTGTA[C/T]GCTCTACCACCATGC | 30945 |
rs31962591 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36261426 | TGTGTGTAGTGACCT[A/G]AATGGTTCACCCTCC | 30945 |
rs31982581 | snp | C/T | 0.444444 | 0.157135 | downstream-variant-500B | Rnf19a, Mir8097 | Mm_Celera | 15:36239601 | CCTTCTAGAGGCAGC[C/T]TAGATAAAAAACATG | 30945 |
rs31983812 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36263553 | ATCTGATAGTAGATT[A/G]TACCTGAGTTTTATA | 30945 |
rs32002808 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36273921 | GATATACCTTATATA[A/G]TCTTCAAAAGCATCA | 30945 |
rs32018694 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36279442 | TTAAACACCTAAAAT[A/T]ATTTCAATGCCTTTT | 30945 |
rs32026988 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36274581 | CCAAGCTGAAACACT[A/C]AGCTCAATCTCTGGA | 30945 |
rs32031184 | snp | C/T | 0.487535 | 0.077957 | intron-variant | Rnf19a | Mm_Celera | 15:36256789 | TTACAAATTTTTATA[C/T]TTTTGAAATTTTTCT | 30945 |
rs32037525 | snp | A/G | 0.401235 | 0.199068 | utr-variant-3-prime, upstream-variant-2KB | Rnf19a, Mir8097 | Mm_Celera | 15:36240229 | AGGTTAGTCTGCCGG[A/G]AGAGCTGTGTGGGAA | 30945 |
rs32038360 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36259043 | GGTCTCTCTGATGGG[A/G]ATTATGCTTGGGCTC | 30945 |
rs32083203 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36274239 | ATGTCTGTCAGATAA[C/T]TCTGGGCCAGAAGGC | 30945 |
rs32091852 | snp | A/G | 0.5 | 0 | intron-variant | Rnf19a | Mm_Celera | 15:36263408 | GCACCCAGCTCATAC[A/G]GTGCTGGAGGTCAGC | 30945 |
rs32108355 | snp | A/G | 0.498615 | 0.0262793 | intron-variant | Rnf19a | Mm_Celera | 15:36252110 | ACTTGTAAACTATTA[A/G]CAGCAGTAATATAAT | 30945 |
rs32115131 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Rnf19a | Mm_Celera | 15:36246382 | AGTCAGGGTAGGAGT[C/T]GGACCTTAACAAGGG | 30945 |
rs32121907 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36246359 | GATGGGAAGGGGTGT[A/G]TGCAGATAGTCAGGG | 30945 |
rs32123887 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36245695 | GTTCCTGGCTTTCAA[C/T]TCCTACATCATCTCA | 30945 |
rs32144299 | snp | A/G | 0.432133 | 0.171253 | intron-variant | Rnf19a | Mm_Celera | 15:36243024 | GAAGAAGCACTGAGT[A/G]AAAATGAAAGTAGTG | 30945 |
rs32150792 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36245868 | ATGAACTATTTAATA[G/T]GTCTCCCTGGCCAGC | 30945 |
rs32154366 | snp | G/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36269333 | ACATGTACAAACATA[G/T]ACCTCATTAGGTCCT | 30945 |
rs32159916 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36274406 | AAAAAAAATTATATT[C/T]AACTGTACAACAAGT | 30945 |
rs32167401 | snp | C/G | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36264176 | GAACATTGTACTTAA[C/G]AAGTTCTTGAAAATT | 30945 |
rs32170385 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36273923 | TATACCTTATATAGT[C/G]TTCAAAAGCATCAGA | 30945 |
rs32179500 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36254812 | CACTTCATATTCACC[A/T]ACGGCACTGTCCACA | 30945 |
rs32181238 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36254841 | CAAACAAACGCACAC[C/T]GTGGAAACTCCCTTT | 30945 |
rs32196889 | snp | C/T | 0.48 | 0.0979796 | missense, upstream-variant-2KB, synonymous-codon | Rnf19a, Mir8097 | GRCm38.p3 | 15:36241968 | CTGTGTGGCCTCGGG[C/T]AGCACCACTGTCATC | 30945 |
rs32197803 | snp | A/C | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36245693 | ATGTTCCTGGCTTTC[A/C]ACTCCTACATCATCT | 30945 |
rs32200274 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36280102 | CCACATGGCAGCTCA[C/T]AGTCATCTGTAACAA | 30945 |
rs32217674 | snp | A/T | 0.455 | 0.143091 | synonymous-codon, upstream-variant-2KB, missense | Rnf19a, Mir8097 | Mm_Celera | 15:36242008 | GCTTCCACTGTTGTG[A/T]CGGAACTTGAATGGC | 30945 |
rs32219176 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36270128 | ATACCAGTTTTTCTC[A/G]GCCACTAGTTTGCAG | 30945 |
rs32235417 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36258168 | AGTGCGGCCCAGTTG[C/T]AGCTGAAGACCCCAG | 30945 |
rs32237169 | snp | A/G | 0.426035 | 0.177515 | intron-variant | Rnf19a | Mm_Celera | 15:36266988 | AAGCTGGAACACATG[A/G]ACACCCAGCATTTTT | 30945 |
rs32251183 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf19a | Mm_Celera | 15:36274341 | AATTATTTAAAAAAA[A/T]ATATATATATCATAT | 30945 |
rs32256774 | snp | A/T | 0.5 | 0 | intron-variant | Rnf19a | Mm_Celera | 15:36263399 | TGCACCAACGCACCC[A/T]GCTCATACAGTGCTG | 30945 |
rs32261887 | snp | C/T | 0.401235 | 0.199068 | utr-variant-3-prime, upstream-variant-2KB | Rnf19a, Mir8097 | GRCm38.p3 | 15:36240450 | TTACTAAAGCCTGAG[C/T]GTGTCTTTGGTAGGT | 30945 |
rs32267487 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36264053 | CTCCTCCATTGGGGG[C/T]CCTGTGATCCATCCA | 30945 |
rs32269054 | snp | C/T | 0.5 | 0 | intron-variant | Rnf19a | Mm_Celera | 15:36263507 | ATGTTTTTGTTGTAA[C/T]AGACACTTAGTATCA | 30945 |
rs32272069 | snp | A/G | 0.475309 | 0.108333 | intron-variant | Rnf19a | Mm_Celera | 15:36255495 | TTCTTAGTGTTTCTT[A/G]TAAAGCTGTTTACAA | 30945 |
rs32272578 | snp | A/G | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36266786 | ACAGAGGACATAACA[A/G]GCACTTCACCAAAGC | 30945 |
rs32274336 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36279635 | AACGGCTCTTGTACC[A/G]TGAATAGCTAGCATG | 30945 |
rs32276564 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf19a | Mm_Celera | 15:36285430 | GGCCTTTGCTCTACC[A/G]TCATAGACTCTAACC | 30945 |
rs32288683 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36251274 | GGTGAAAGTATAAGC[C/T]CAATAAGTCTTTCCC | 30945 |
rs32300452 | snp | A/G | 0.391111 | 0.206368 | intron-variant | Rnf19a | Mm_Celera | 15:36262758 | CATGAAGAATACTAA[A/G]AAAACCACATTCTTC | 30945 |
rs32319588 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36251378 | TCTGGCAATAGCATA[A/G]ATAAGTACTTTCTCC | 30945 |
rs32331611 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36258887 | CCCCATGAGTCCCAG[C/T]TGGTTGATTCTGTGG | 30945 |
rs32333545 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Rnf19a | Mm_Celera | 15:36254839 | CACAAACAAACGCAC[A/G]CTGTGGAAACTCCCT | 30945 |
rs32337784 | snp | A/G | 0.444444 | 0.157135 | upstream-variant-2KB | Rnf19a | Mm_Celera | 15:36285240 | TCAAGAAATATTGCT[A/G]TCTACTAAATTAAAA | 30945 |
rs32348388 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36273306 | TTTCTAATTTTCCTA[C/T]CCCTCCTCACCCCTT | 30945 |
rs32364795 | snp | A/G | 0.495 | 0.0497494 | intron-variant | Rnf19a | Mm_Celera | 15:36254756 | AGTTCAGAACTGTAT[A/G]CTGCTCTTTCAGTGA | 30945 |
rs32400270 | snp | A/C | 0.444444 | 0.157135 | intron-variant | Rnf19a | Mm_Celera | 15:36273169 | ACACACACACACACG[A/C]TCTCTGATGAACTTG | 30945 |
rs32415312 | snp | C/T | 0.375 | 0.216506 | intron-variant | Rnf19a | Mm_Celera | 15:36243727 | CTTCACGTTTAAAAA[C/T]AGCAGTAGGTACATT | 30945 |
rs32425654 | snp | C/T | 0.48 | 0.0979796 | synonymous-codon, upstream-variant-2KB, missense | Rnf19a, Mir8097 | GRCm38.p3 | 15:36242047 | AATATCCACTTGCAC[C/T]TCCATGCTGTTCCCT | 30945 |