SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3089138 | snp | A/G | 0.15879 | 0.232768 | intron-variant | Wdfy4 | Mm_Celera | 14:33038447 | TATTTTGTATGTAGT[A/G]GGCAGGTGTGAACAT | 545030 |
rs3669686 | snp | C/T | 0.42 | 0.183303 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:33003239 | CAAGAAAACAGGGCT[C/T]ACTTGGAACCCTCTT | 545030 |
rs3671016 | snp | A/G | 0.359862 | 0.224567 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:33003490 | TCCCTGAAATAGACT[A/G]TCTCATGGTACTGCC | 545030 |
rs3682198 | snp | A/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33171616 | AATGGGCAACACCCG[A/T]AATGGGAATACTGCC | 545030 |
rs3696856 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33171640 | TACTGCCCCCCAGAC[C/T]ATAAATATAAATATA | 545030 |
rs3697496 | snp | A/G | 0.255 | 0.24995 | intron-variant | Wdfy4 | Mm_Celera | 14:33171790 | GGTGGAACAAGGCAA[A/G]GATCGGGTCACCTCA | 545030 |
rs3698967 | snp | A/G | 0.244898 | 0.249948 | upstream-variant-2KB | Wdfy4 | GRCm38.p3 | 14:33195481 | TACACTGTGGCTATC[A/G]CTACTTATAAAAGCA | 545030 |
rs3699402 | snp | A/G | 0.5 | 0 | upstream-variant-2KB | Wdfy4 | GRCm38.p3 | 14:33195509 | GCAGATTCCTATGTG[A/G]AAAGGAATTCTCTGT | 545030 |
rs3700001 | snp | A/G | 0.231111 | 0.249285 | upstream-variant-2KB | Wdfy4 | GRCm38.p3 | 14:33195591 | GCTCTGCAGCCATTC[A/G]AACTCAACAGCAGAT | 545030 |
rs3700643 | snp | C/T | 0.231111 | 0.249285 | upstream-variant-2KB | Wdfy4 | Mm_Celera | 14:33195729 | CTGTCTTGCATTGGG[C/T]ATGTCACTTCAGCTG | 545030 |
rs3700691 | snp | A/C | 0.244898 | 0.249948 | upstream-variant-2KB | Wdfy4 | Mm_Celera | 14:33195756 | GCTGTTTAATTAGAC[A/C]TACTGGCGTCTAAAA | 545030 |
rs3700734 | snp | C/T | 0.5 | 0 | upstream-variant-2KB | Wdfy4 | GRCm38.p3 | 14:33195777 | GCGTCTAAAAGTCCT[C/T]CTTACAGGGAGGCCA | 545030 |
rs6196268 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33034772 | AGATGGGAAAGGACA[A/G]GCNTTTGAAAGTGCA | 545030 |
rs6196274 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33034775 | TGGGAAAGGACANGC[A/G]TTTGAAAGTGCAGTG | 545030 |
rs6196767 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33034828 | GCATGGGAGAGACTA[A/G]GTCACAAAGAGGTAA | 545030 |
rs6196825 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33034863 | AAGGCTGGATTAGGG[C/T]TAacatacatacata | 545030 |
rs6196857 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33034883 | atacatacatacata[C/T]atacatacatacata | 545030 |
rs6197388 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33034964 | TTCTGTATAATTAGG[A/G]AAAGGGCCAGCcatg | 545030 |
rs6201250 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdfy4 | Mm_Celera | 14:33159083 | CAACACTCTACACTC[A/G]AGGATCCCAGCACTC | 545030 |
rs6202474 | snp | A/G/T | 0.5 | 0 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:32995837 | TTTGTTTGGGCTGGT[A/G/T]CTTGGCNTCACTAGC | 545030 |
rs6202492 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:32995844 | GGGCTGGTNCTTGGC[A/G]TCACTAGCTTCTTTG | 545030 |
rs6211822 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33035297 | ACTTCTCCCTTTGAT[C/T]TGGCTATCACAGTCC | 545030 |
rs6211933 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114280 | TGTCCAGAGGACATC[A/G]CCAGAACGGAGCTAA | 545030 |
rs6211956 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdfy4 | Mm_Celera | 14:33114306 | GCTAAATCCAGTACC[A/G]CAACCAGAAGATTTT | 545030 |
rs6211962 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33035394 | AGATAATAACAAACA[A/G]CAGAGAGAATCTAAC | 545030 |
rs6212448 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdfy4 | Mm_Celera | 14:33114381 | TATAGTAACAGAAGA[C/T]GGGCTCANAGAGCTA | 545030 |
rs6212452 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114389 | CAGAAGANGGGCTCA[C/T]AGAGCTAAGCCTGTT | 545030 |
rs6212474 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114405 | AGAGCTAAGCCTGTT[C/T]AGGGAGCCGATGTGT | 545030 |
rs6225450 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33114498 | TTCTTCCAGAACTCA[C/T]ACAGAACCAGGGGCT | 545030 |
rs6226085 | snp | C/G | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114658 | ACTCTCTGGGGAGAG[C/G]AGGACTTCATAGGCT | 545030 |
rs6226567 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114714 | TTGCTTACCTAGAAT[C/T]GATTCTTTCTTTCCA | 545030 |
rs6226666 | snp | A/C | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114762 | CTTGCCACAGTCCCA[A/C]CAGCATGGCACGTTC | 545030 |
rs6227096 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114789 | GTTCATTTGTGCCAA[C/T]AGCATCCTAGGCTTG | 545030 |
rs6227157 | snp | A/G | 0.345679 | 0.230967 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33114820 | GGAGTTTGTGGTCTT[A/G]GGTTAAGTGTATCTT | 545030 |
rs6240167 | snp | G/T | 0.5 | 0 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:32998130 | aaaaggactgcttca[G/T]attgtccacagcagc | 545030 |
rs6245929 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33115963 | gctctccctttctct[C/T]acattcttccctctc | 545030 |
rs6247448 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116182 | CTGACAAAGAATGGG[A/G]ATCAATTGGTCCACC | 545030 |
rs6247991 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116308 | GAGCAGAGCCTGGAG[C/G]GGGATCAAAAAGTCA | 545030 |
rs6248010 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116315 | GCCTGGAGCGGGATC[A/G]AAAAGTCACAGGGCA | 545030 |
rs6248014 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116319 | GGAGNGGGATCNAAA[A/G]GTCACAGGGCATACC | 545030 |
rs6248060 | snp | A/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116348 | CCTGTGACAACATGA[A/T]GGTCTCTGGACACCA | 545030 |
rs6248627 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116468 | GCCTCAGATTGCCAG[C/T]CCTGAAGAGCTAGGA | 545030 |
rs6263492 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116977 | GCCATGCTGCAAGCT[A/G]GGACTCCAGTGAGTC | 545030 |
rs6263965 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33117045 | GGGGCTCACTTCGTC[C/T]CACAATGGAATACCC | 545030 |
rs6264394 | snp | C/T | 0.495868 | 0.0452663 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33117084 | TCTGGATCCCTATTG[C/T]GATTGCAAAATGTGC | 545030 |
rs6264873 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33117181 | TCAGGTATGGACCTG[A/G]TAATCCCACTGAGTT | 545030 |
rs6264979 | snp | A/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33117249 | AGGAACCTCCCCTTC[A/T]CCTCCTCCCATCTCT | 545030 |
rs6278910 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33117484 | GGAACCATGACGTTG[A/G]GGCCTGAAACACTTC | 545030 |
rs6313860 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33060327 | TTTCTTATACTCTCC[C/T]CATNCTGTCTTCTAT | 545030 |
rs6313866 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Wdfy4 | Mm_Celera | 14:33060331 | TTATACTCTCCNCAT[A/G]CTGTCTTCTATGTTC | 545030 |
rs6396384 | snp | A/G/T | 0.444444 | 0.157135 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33149424 | AGCAAGATGATTCTG[A/G/T]GCCCCACAGCTTGAG | 545030 |
rs6396413 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33149442 | CCCACAGCTTGAGGG[A/G]TGCTGTTTCTCTCCC | 545030 |
rs6410697 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdfy4 | Mm_Celera | 14:33149696 | GGGAAGCACAGCCCT[C/G]CTGAGCCAGGAAGCA | 545030 |
rs6410709 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdfy4 | Mm_Celera | 14:33149705 | AGCCCTGCTGAGCCA[A/G]GAAGCAGGGGTTTCT | 545030 |
rs6410727 | snp | G/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:33149715 | AGCCANGAAGCAGGG[G/T]TTTCTGCTGCTGCTC | 545030 |
rs13482129 | snp | A/T | 0.498398 | 0.0282565 | missense | Wdfy4 | GRCm38.p3 | 14:33093247 | CTACTCACTCAGAGG[A/T]CAGATGAAGTTGGGA | 545030 |
rs30103088 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdfy4 | Mm_Celera | 14:32986192 | TGCCCACAGGGGGCA[G/T]AAGAGGACATTGGAT | 545030 |
rs30106532 | snp | C/G | 0.48 | 0.0979796 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:32996369 | GCTGGCTCGAAGACG[C/G]GGTAGGGTGTGGCCC | 545030 |
rs30108085 | snp | C/T | 0.475309 | 0.108333 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33043325 | GGACACCCTACACTG[C/T]TTTTGAAGGCCATAC | 545030 |
rs30111209 | snp | A/G/T | 0.375 | 0.216506 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33026271 | TGCCCAACAATCCAC[A/G/T]GACAGGAAGTGAGTG | 545030 |
rs30115404 | snp | C/T | 0.444444 | 0.157135 | utr-variant-3-prime | Wdfy4 | Mm_Celera | 14:32959773 | CATGTTTAGGGTACA[C/T]GGTGCAAACCATCAG | 545030 |
rs30123565 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | Mm_Celera | 14:32974014 | ATTCCATGTCAATGA[C/T]ATCACCTTACCCTAG | 545030 |
rs30127723 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33161793 | CCCTAGAGGTGAACT[C/T]GATTTCTGACTCATC | 545030 |
rs30140519 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdfy4 | GRCm38.p3 | 14:32984984 | CTCCAGCACTGGTTC[A/G]TCTCCAGCTCCCTCA | 545030 |
rs30143396 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33101482 | TCCCCAAAGCAAAGC[A/G]GAGTCTAGTGCTTGA | 545030 |
rs30143443 | snp | C/T | 0.5 | 0 | intron-variant | Lrrc18, Wdfy4 | GRCm38.p3 | 14:33001791 | TTTAGCTATCAGAAT[C/T]ATCTACATTTGACTT | 545030 |
rs30144239 | snp | C/G | 0.444444 | 0.157135 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33056600 | GGCATGGGGATGTCA[C/G]ATTAAGTGGCAATTT | 545030 |
rs30145409 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33108360 | GACCAGCTCTGCCCA[A/G]TACAGCACCTGGTAC | 545030 |
rs30146855 | snp | C/G | 0.375 | 0.216506 | intron-variant | Wdfy4 | Mm_Celera | 14:33044554 | TGGGTCAAGTGGAGG[C/G]TGGAGGAGTCTTGTT | 545030 |
rs30147793 | snp | A/G | 0.5 | 0 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:33001132 | GCACTCTCTGGGGCA[A/G]AAGTGCGACTGCTTA | 545030 |
rs30150825 | snp | C/T | 0.33241 | 0.236027 | intron-variant | Wdfy4 | Mm_Celera | 14:33108101 | CCACATTGACTTGAG[C/T]GGTGTCCTCCATGTC | 545030 |
rs30155559 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33094383 | GGCGATGTCAGAATG[C/T]CTGTTGCTCTCCACT | 545030 |
rs30156361 | snp | G/T | 0.5 | 0 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33116761 | AACTCAACCTCTCTT[G/T]ATAAGGCTGCTCCTG | 545030 |
rs30156827 | snp | C/T | 0.359862 | 0.224567 | intron-variant | Wdfy4 | Mm_Celera | 14:33189523 | ACCAGTTGCTGGCTT[C/T]CTCCTCATAGACCCT | 545030 |
rs30158995 | snp | C/T | 0.498615 | 0.0262793 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33070257 | GGGCCAGACCTAGTG[C/T]TACAATCTCACAAGC | 545030 |
rs30163869 | snp | G/T | 0.375 | 0.216506 | intron-variant | Wdfy4 | Mm_Celera | 14:33065162 | TGTTTCATTAAGCTC[G/T]TCAACATCTCTGACT | 545030 |
rs30167391 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdfy4 | Mm_Celera | 14:33177802 | AGAGGATGAACTGGG[A/G]AGAAAATTAACCTTA | 545030 |
rs30174504 | snp | G/T | 0.444444 | 0.157135 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33138785 | GGCAATGCGATAACA[G/T]GAGCGAGTCCCTCAA | 545030 |
rs30178330 | snp | C/T | 0.375 | 0.216506 | synonymous-codon | Wdfy4 | Mm_Celera | 14:33133517 | CAGCAGACAGAGGTC[C/T]TCAGCCAGCTTCTCA | 545030 |
rs30188077 | snp | A/T | 0.375 | 0.216506 | intron-variant | Wdfy4 | Mm_Celera | 14:33036630 | GATAAAAGAATCCAA[A/T]AAAGTAGCCAAAAGT | 545030 |
rs30189602 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdfy4 | Mm_Celera | 14:33174954 | ACCCTACACTGTCAG[A/G]TTTAGGGACATGGAT | 545030 |
rs30203154 | snp | G/T | 0.493827 | 0.0552116 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33133166 | CACACACCCACTGGT[G/T]ACCCACAGCAGAAGT | 545030 |
rs30205605 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Wdfy4 | Mm_Celera | 14:33035263 | GAAGAGCTTGTGAGC[A/G]ATGCTGTCCAGAGCA | 545030 |
rs30205665 | snp | A/G | 0.42 | 0.183303 | intron-variant, synonymous-codon | Wdfy4 | Mm_Celera | 14:33080740 | GAACCCCTCCGCAGC[A/G]TGGCTGGCTTCAGCA | 545030 |
rs30207727 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33129947 | GACTCTAGTAGCACA[A/C]GAAATAGTTCCAAGA | 545030 |
rs30212003 | snp | A/G | 0.475309 | 0.108333 | upstream-variant-2KB, intron-variant | Wdfy4 | GRCm38.p3 | 14:33186009 | AGAAGCTTAGAGAAA[A/G]TCAGAAACGTCTTTG | 545030 |
rs30212509 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdfy4 | Mm_Celera | 14:32985586 | TCAGAGAGGAAGCAC[C/T]GTCATTATCCAAGCC | 545030 |
rs30215518 | snp | C/T | 0.277778 | 0.248452 | intron-variant | Wdfy4 | Mm_Celera | 14:33043635 | GCAGGGATTGCCCTG[C/T]AGATATGTGGCCTGA | 545030 |
rs30223880 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33089648 | CTACAAGCAAGAGTG[A/G]GAGGTGGGAGTTAAA | 545030 |
rs30224671 | snp | A/G | 0.33241 | 0.236027 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33045633 | CTGAACTTAATAGCC[A/G]CATTGCTCACTCAGA | 545030 |
rs30237744 | snp | A/G | 0.21875 | 0.248039 | intron-variant | Wdfy4 | Mm_Celera | 14:33187464 | CCTTTATATTGTCTC[A/G]CTGATCATGTGGCAT | 545030 |
rs30243429 | snp | C/T | 0.456747 | 0.140554 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33079094 | TGTAAAGCAGATATC[C/T]AGAGTCATTTACACA | 545030 |
rs30244661 | snp | C/G | 0.345679 | 0.230967 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:33001531 | CACACTTGGATCCTA[C/G]TGTCACAAAGGCTAC | 545030 |
rs30245491 | snp | C/T | 0.48 | 0.0979796 | intron-variant | Wdfy4 | Mm_Celera | 14:33092903 | AACCCTTTCTCCATT[C/T]TGTTGCCTGCCAGGT | 545030 |
rs30246029 | snp | A/C | 0.42 | 0.183303 | intron-variant | Wdfy4 | Mm_Celera | 14:33108766 | TGCAGGCAAGCTCTT[A/C]CAGACCACTTCCCTA | 545030 |
rs30246933 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdfy4 | Mm_Celera | 14:33129793 | TTTAAAGCCTGAAAC[A/C]TGAACCTGCTAAAGG | 545030 |
rs30250296 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdfy4 | GRCm38.p3 | 14:33044988 | GCCTGAGATGTCTAC[A/G]TAGGGAATTCCAGGC | 545030 |
rs30251474 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdfy4 | Mm_Celera | 14:33065661 | ATGATGGCTGGGGTG[A/G]CAGGGAGGTGAAAGG | 545030 |
rs30251480 | snp | A/G | 0.375 | 0.216506 | intron-variant | Lrrc18, Wdfy4 | Mm_Celera | 14:33000421 | GATAGCTGCCGGATC[A/G]ATGGGCGATCACCAT | 545030 |
rs30252804 | snp | C/T | 0.401235 | 0.199068 | intron-variant | Wdfy4 | Mm_Celera | 14:33175191 | CTGACCACAGCTGTC[C/T]TCTGGGCACCAGAGA | 545030 |