SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs3692549 | snp | G/T | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79764683 | AGGGCAGGGTGTGAG[G/T]GAGAAAGATAAGACA | 69368 |
rs3693205 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79764801 | TCACAGTCCTCCTGC[C/T]TCAGATTCCCTAGTG | 69368 |
rs3693210 | snp | A/C | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79764804 | CAGTCCTCCTGCCTC[A/C]GATTCCCTAGTGCTG | 69368 |
rs3694279 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79764915 | GGACAACATGTGTAC[A/G]TGTGGAACCAGGGCT | 69368 |
rs3694327 | snp | A/C | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79764946 | TCACACATGTCAGTC[A/C]TGTGCACTCCCACTC | 69368 |
rs3694408 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79764985 | CCCCCCCTGCTTCTT[C/T]CATTTTACTTTCTGT | 69368 |
rs3694906 | snp | A/T | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79765020 | AGACTGATGCTCCAT[A/T]CATTGCCCAGGTTGT | 69368 |
rs3694921 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79765038 | TTGCCCAGGTTGTCC[C/T]GGAACCAACTCCATT | 69368 |
rs3695018 | snp | A/C | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79765097 | CTCCTGACTCAAAAG[A/C]TGGATTAGAGGCCTC | 69368 |
rs3718571 | snp | A/G | 0.415225 | 0.187619 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79714767 | AGTGGTGACCTCATC[A/G]GACTAAGAAGGGAGA | 69368 |
rs6157189 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79766697 | AAGCAATTTATGTAA[A/G]CAAAATAAGTTTTAA | 69368 |
rs6157668 | snp | A/G | 0.48 | 0.0979796 | intron-variant | Wdfy1 | Mm_Celera | 1:79766742 | TATACCATATTTCAT[A/G]AAATCAGTGTTCAAA | 69368 |
rs6158311 | snp | A/C | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79766870 | tcaacctgtgatttc[A/C]catccttttgagggt | 69368 |
rs6195176 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79769016 | tgtggttgctgggaa[C/T]tggactcaggacctc | 69368 |
rs6195249 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79769063 | gctcttaaccactga[A/G]ccatctctccagccc | 69368 |
rs6266723 | snp | C/T | 0.429688 | 0.173817 | intron-variant | Wdfy1 | Mm_Celera | 1:79747250 | GTAAACAAGCCTTTC[C/T]AGAAATTTCCANATA | 69368 |
rs6266741 | snp | C/T | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79747262 | TTCNAGAAATTTCCA[C/T]ATATTTCCTGCTAAA | 69368 |
rs6266775 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Wdfy1 | Mm_Celera | 1:79747283 | TCCTGCTAAAGCATT[A/G]ACTCCTAAGCAAAGG | 69368 |
rs6278577 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79752713 | tgaagcaacatatat[A/G]tggggtgtgatggct | 69368 |
rs6279064 | snp | A/T | 0.207612 | 0.24638 | intron-variant | Wdfy1 | Mm_Celera | 1:79752824 | ctgaggccagcctag[A/T]atacatgagagaact | 69368 |
rs6279172 | snp | A/T | 0.444444 | 0.157135 | intron-variant | Wdfy1 | Mm_Celera | 1:79752893 | AGTATAAAAAAACAC[A/T]CCATCAAGTGAGTAA | 69368 |
rs6279539 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Wdfy1 | Mm_Celera | 1:79747334 | ACCAGCAAAGTATGG[C/T]GATGgccatcagaat | 69368 |
rs6279997 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79747391 | tggtgctgataacac[A/G]caacaagggctgcgg | 69368 |
rs6280027 | snp | A/G | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79747409 | acaagggctgcggct[A/G]atggcagccagcgat | 69368 |
rs6280585 | snp | A/T | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79747514 | cagtaacttcacaca[A/T]acaaatacatacata | 69368 |
rs6281816 | snp | G/T | 0.5 | 0 | intron-variant | Wdfy1 | Mm_Celera | 1:79747770 | cctacacatacatgt[G/T]agtgcaagagggcat | 69368 |
rs6318972 | snp | C/G | 0.304688 | 0.243945 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79703755 | TTGTGGTTTCACGAC[C/G]TCACCCACTCTCTTG | 69368 |
rs6319007 | snp | C/G | 0.290657 | 0.246672 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79703783 | TTGTCCAAAGCACTG[C/G]AGCAATCCACATCTT | 69368 |
rs13463168 | snp | C/T | | | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79705105 | GAGAGTACTCAGATA[C/T]ACAACCAGGGGCTGG | 69368 |
rs13468192 | snp | C/T | 0.391111 | 0.206368 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79703833 | AGCGTCACTTTTAAC[C/T]GCTGGTTTTTCATTG | 69368 |
rs13472765 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Mrpl44, Wdfy1 | GRCm38.p3 | 1:79776303 | CTGCCCGCCGCCGCC[A/G]GTGCGACGGTAGGCG | 69368 |
rs13472766 | snp | A/G | | | synonymous-codon, upstream-variant-2KB | Mrpl44, Wdfy1 | Mm_Celera | 1:79777888 | CTGGGATTACCATGC[A/G]GAGGTACAAGCCTTT | 69368 |
rs13472767 | snp | A/C | | | frameshift-variant, upstream-variant-2KB | Mrpl44, Wdfy1 | Mm_Celera | 1:79776180 | GGCCCTCGCCGCCTA[A/C]TTGGCTCCGGCCGTC | 69368 |
rs30149984 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79737219 | TCCTTCTCTAACTGG[G/T]AACCACCTCAGGAAA | 69368 |
rs30149985 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79737174 | GTTAGCCAGCTATGG[C/T]GGAGCCCAGGGACTA | 69368 |
rs30149986 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79737159 | ACTGGGCATGCTGGT[A/G]TTAGCCAGCTATGGT | 69368 |
rs30149987 | snp | A/C | 0.21875 | 0.248039 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79737105 | TTAAAATGCAGCAGC[A/C]ACAGCAGCTGGAACC | 69368 |
rs30149988 | snp | A/C/G | 0.132653 | 0.220748 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736751 | CAGGGCAATACGAAG[A/C/G]GTTACCTTGCTCACA | 69368 |
rs30149989 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736627 | AAGGAAAAAAGGCTG[A/G]GTGCATAAAGTAAGA | 69368 |
rs30149990 | snp | A/C | 0.497778 | 0.0332592 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736526 | GTCAGAATTACAGCC[A/C]TAAGCAATCGACTTA | 69368 |
rs30149991 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736435 | CTTTGCCATCCAGTC[C/T]TGCACATAAGACATT | 69368 |
rs30149992 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736395 | TGAGCGCCTGCCATA[A/G]ACTGTCTGGTCCATG | 69368 |
rs30149993 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736344 | GGAGGGCCTTCACTG[C/T]TCAGCATTGCTTTCG | 69368 |
rs30150814 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736277 | AAAACTCAGAGCAGA[C/G]TGCCAAATGCACCCA | 69368 |
rs30150815 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736270 | TATATGTAAAACTCA[A/G]AGCAGACTGCCAAAT | 69368 |
rs30150816 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736235 | TATATACACAAAAGG[C/T]ACCTATGAGTCTGAG | 69368 |
rs30150817 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736118 | AAGAGGTTTCTAGTA[A/G]GGTAAGCAATATACA | 69368 |
rs30150818 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736094 | TTTATTTATTTATTT[A/G]TCCTGGATAAGAGGT | 69368 |
rs30150819 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79736022 | GTAGCTATCCACCAG[C/T]CGTCTCATAGACCTA | 69368 |
rs30150820 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735895 | GCTGCTGTTGCTGGC[C/T]TGTATGAGTAATGCA | 69368 |
rs30150821 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735822 | TATGCCTAACACTAT[C/G]ATAAAACCCTCATTT | 69368 |
rs30150822 | snp | A/G | 0.244898 | 0.249948 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735799 | TGGCTTTAAAGATCA[A/G]TTCTTCTTATGCCTA | 69368 |
rs30150823 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735795 | ATGTTGGCTTTAAAG[A/G]TCAGTTCTTCTTATG | 69368 |
rs30151704 | snp | A/G | 0.18 | 0.24 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735774 | TACAGCTGATGATAA[A/G]TTTTGATGTTGGCTT | 69368 |
rs30151705 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735638 | TGTTAGGCTCTCTGA[A/G]TTAAAAGATAATTAT | 69368 |
rs30151706 | snp | C/T | 0.18 | 0.24 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735421 | GAAGGTAGATACTGA[C/T]ATTATACAAAATTCA | 69368 |
rs30151707 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735364 | AAAGCAATTTTAGAC[C/T]ATCCTAGGACTACTT | 69368 |
rs30151708 | snp | A/C/T | 0.46875 | 0.121031 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735344 | CATAACACAAAATTG[A/C/T]ACTCAAAGCAATTTT | 69368 |
rs30151709 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79735320 | GGGCTCATACTCTGC[C/T]CAAGAAAACATAACA | 69368 |
rs30151710 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734645 | GAAAATAAACCAGAC[A/G]TGTGCCGCTTGAATT | 69368 |
rs30151711 | snp | C/T | 0.444444 | 0.157135 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734624 | ACTGGAAAACGCATG[C/T]CAGGGGAAAATAAAC | 69368 |
rs30151712 | snp | C/T | 0.336735 | 0.234472 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734560 | GTTTGGAAACAACTG[C/T]TTGGGTTCACTCAGC | 69368 |
rs30151713 | snp | C/T | 0.21875 | 0.248039 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734525 | GAAATTTGGAAGGAA[C/T]GAGATTTCTAAAACT | 69368 |
rs30152474 | snp | A/G | 0.493827 | 0.0552116 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734381 | CGTTGTAGTGAGCAG[A/G]GCTGTGGCTGTATTA | 69368 |
rs30152475 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734366 | GCAACAGCACACACC[C/T]GTTGTAGTGAGCAGA | 69368 |
rs30152476 | snp | C/G | 0.277778 | 0.248452 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734158 | AGTACCATGGATGCT[C/G]CTCCAGGAACCAGTG | 69368 |
rs30152477 | snp | A/C | 0.375 | 0.216506 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734129 | ACGCAGTCTCATCTG[A/C]GTGGAACTCCTACAG | 69368 |
rs30152478 | snp | C/G | 0.5 | 0 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79734115 | TGAAGTGAGGCAGCA[C/G]GCAGTCTCATCTGCG | 69368 |
rs30152479 | snp | A/T | 0.345679 | 0.230967 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733972 | TATGTGGGTTAGGTT[A/T]AAAAATTAGACAAAA | 69368 |
rs30152480 | snp | A/T | 0.48 | 0.0979796 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733934 | GAAGGCATTGCTTAA[A/T]GTACACTGCTATCAA | 69368 |
rs30152481 | snp | A/G | 0.375 | 0.216506 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733780 | TACGCAGGACATACT[A/G]AACACATGGACCTAC | 69368 |
rs30152482 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733739 | GACAAACAACCTGCT[C/T]GGCATAAGTAATCAT | 69368 |
rs30152483 | snp | C/T | 0.497041 | 0.0383476 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733613 | TGCGGGTGACCCGTG[C/T]AGACTCTAACCATGA | 69368 |
rs30153194 | snp | A/G | 0.444444 | 0.157135 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733513 | CTTACAGAAACACAC[A/G]TACACAGAGGTTCTT | 69368 |
rs30153195 | snp | A/T | 0.396694 | 0.202437 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733434 | AAAGGGGGCTCGAGG[A/T]ACACTGCTTTCCCTC | 69368 |
rs30153196 | snp | C/T | 0.46875 | 0.121031 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733379 | ACTCAAAGGCAACAG[C/T]CAATAACAGACTGAA | 69368 |
rs30153197 | snp | A/G | 0.495868 | 0.0452663 | intron-variant | Wdfy1 | GRCm38.p3 | 1:79733243 | TTCCAAAGTGGTGGT[A/G]CTGACTTGACCTAAT | 69368 |
rs30153198 | snp | A/C | 0.493827 | 0.0552116 | intron-variant | Wdfy1 | Mm_Celera | 1:79732307 | GTATTCCTATGAAAA[A/C]GAGACATGACCTGAA | 69368 |
rs30153199 | snp | C/T | 0.396694 | 0.202437 | intron-variant | Wdfy1 | Mm_Celera | 1:79732274 | TGGGCACATTCAGAG[C/T]GATGGCCACAGATTC | 69368 |
rs30153200 | snp | A/G | 0.277778 | 0.248452 | intron-variant | Wdfy1 | Mm_Celera | 1:79732234 | TAGAAGAAAGGACAA[A/G]TGTGAAGTATCTGTT | 69368 |
rs30153201 | snp | C/T | 0.35503 | 0.226867 | intron-variant | Wdfy1 | Mm_Celera | 1:79732182 | TCATTCAGTGTCACC[C/T]GGCTAAGATACCCTC | 69368 |
rs30153202 | snp | C/T | 0.165289 | 0.235211 | intron-variant | Wdfy1 | Mm_Celera | 1:79732140 | CGACATCCATGTTGT[C/T]TCAGGAGTTCCTGGG | 69368 |
rs30153203 | snp | A/C/T | 0.277778 | 0.248452 | intron-variant | Wdfy1 | Mm_Celera | 1:79731506 | GACATCTTCCTTGAT[A/C/T]CTCTCAAACTCAGCC | 69368 |
rs30153514 | snp | A/G | 0.32 | 0.24 | intron-variant | Wdfy1 | Mm_Celera | 1:79744636 | GAGGACTCCACCACC[A/G]ATCGAGGGCACAGAG | 69368 |
rs30153515 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Wdfy1 | Mm_Celera | 1:79744469 | ACTTGAGATGGAAGT[A/G]TATCTTTCTTTTTTT | 69368 |
rs30153516 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Wdfy1 | Mm_Celera | 1:79744401 | AATGCTTTAGAATCA[C/T]TAGGGTTTTTTCCAA | 69368 |
rs30153517 | snp | C/T | 0.32 | 0.24 | intron-variant | Wdfy1 | Mm_Celera | 1:79744292 | ACCTAAGTCGGGTCC[C/T]GTTTTCCTCAACACC | 69368 |
rs30153518 | snp | A/C | 0.124444 | 0.216185 | intron-variant | Wdfy1 | Mm_Celera | 1:79744263 | TTTACTACCTGACAA[A/C]TCTCTACTCCCACAC | 69368 |
rs30153519 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Wdfy1 | Mm_Celera | 1:79744228 | TACTGAAACTGTTTC[C/T]TAAACCAACAGAGTA | 69368 |
rs30153520 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Wdfy1 | Mm_Celera | 1:79744182 | CTGGTGGGTCTGTGG[C/G]CCGTAAGCCCAGTGC | 69368 |
rs30153521 | snp | A/C | 0.244898 | 0.249948 | intron-variant | Wdfy1 | Mm_Celera | 1:79744148 | TAGTAAGCGAGCTAC[A/C]CTAAGTACTGAGTGA | 69368 |
rs30153522 | snp | G/T | 0.32 | 0.24 | intron-variant | Wdfy1 | Mm_Celera | 1:79744051 | TGACCACTCAGCAAA[G/T]TAGAAGCAAAGCCTG | 69368 |
rs30153523 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Wdfy1 | Mm_Celera | 1:79743858 | TCAGCAAAGTTTCCC[A/T]ATGTTAAAAGTTACC | 69368 |
rs30153574 | snp | G/T | 0.48 | 0.0979796 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79704196 | AAAGTGATAAAGCCT[G/T]AGTCCTCTCTGGCAG | 69368 |
rs30153575 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79703754 | ATTGTGGTTTCACGA[C/T]GTCACCCACTCTCTT | 69368 |
rs30153576 | snp | C/G | 0.497041 | 0.0383476 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79703204 | ACTCTCTTAAGTGAT[C/G]TGTTTAGCAACAGAA | 69368 |
rs30153577 | snp | A/G | 0.124444 | 0.216185 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79702988 | GTGGTTTCTACCAAC[A/G]TACAGGCCTATTGCT | 69368 |
rs30153578 | snp | G/T | 0.124444 | 0.216185 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79702726 | TAACAGTAACTTGAT[G/T]CTTGTCATTTAGGAG | 69368 |
rs30153579 | snp | C/T | 0.124444 | 0.216185 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79702578 | AGAGTTATTGTGTAG[C/T]AAACTGCAGAAAATA | 69368 |
rs30153580 | snp | C/T | 0.132653 | 0.220748 | utr-variant-3-prime | Wdfy1 | GRCm38.p3 | 1:79702550 | TTGCACGATTAAACT[C/T]CAACTTATTCAAAGA | 69368 |