At4g18490
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346452462snpA/Tintron-variant?TAIR104:10204928CACCTAAATAAATGT[A/T]GTTCAATCGTGAAAT827581
rs346469166snpG/Tintron-variant?TAIR104:10207004AAGCTTCCTTGCTTT[G/T]GGATTTCTGTCACAG827581
rs346519123snpC/Gmissense?TAIR104:10207901AGAACATAAACATGG[C/G]AAATCTGGAAATCCC827581
rs346580082snpA/Tmissense?TAIR104:10205918TGGAATCAAGTTATG[A/T]GAAGATAGAACAGAC827581
rs346597561snpC/Tmissense?TAIR104:10205081ATTTTGGATCATCAT[C/T]TAAAATGGACATGCC827581
rs346654879snpC/Tintron-variant?TAIR104:10206899GTTTGCTATCTCTTG[C/T]CATGCTCTTGATTCC827581
rs346679766snpA/Gmissense?TAIR104:10204801TGGAACTTCAAGTCA[A/G]TGACAGATGATGATC827581
rs346713903snpG/Tintron-variant?TAIR104:10203974TCGTTGTCCCTGAAA[G/T]TTAGTCTCGAGTGGC827581
rs346731179snpC/Gintron-variant?TAIR104:10203881CTGTGTTAGAGGTGA[C/G]GTTTATGCGTAGATT827581
rs346737743snpC/Tmissense?TAIR104:10207376AGATTCATCATTTGG[C/T]TCCTAGGGACAAAAC827581
rs346740610snpA/Cmissense?TAIR104:10206019ACTCAGGCAGAAATA[A/C]AGGATAACACTAAAG827581
rs346789601snpA/Cintron-variant?TAIR104:10204014CTTAAAATCGACGAA[A/C]CGCCTGGTTATTTTT827581
rs346824068snpA/Cintron-variant?TAIR104:10206933AACAGGCTATTACCC[A/C]ATGTGCACTCATTGT827581
rs346824681snpC/Tsynonymous-codon?TAIR104:10204393AGATATTGCCATGTC[C/T]GCACCTGCTAAAAGA827581
rs346845448snpC/Tintron-variant?TAIR104:10206889TTTAATACCTGTTTG[C/T]TATCTCTTGCCATGC827581
rs346852106snpA/Gmissense?TAIR104:10205995CAACAGGAAGAAATG[A/G]GTACAGACACTCAGG827581
rs346890807snpA/Cmissense?TAIR104:10207831GAGAGTAGAATAGAT[A/C]CTAAGACGACCAAGG827581
rs346906417snpA/Cmissense?TAIR104:10207294CCGAGTTCTGCAGTG[A/C]AACCAGAATTTAGCT827581
rs346924168snpA/Cintron-variant?TAIR104:10206477TCTTCACCTGTGTAA[A/C]TATATCTTTTCACTC827581
rs346926867snpC/Tmissense?TAIR104:10207154TGGCTGATCTGCGTG[C/T]AGTGAAAACTCAAAG827581
rs346956868snpA/Gutr-variant-5-prime?TAIR104:10203710ACGTTTATCGTTAGC[A/G]CCTACTACATATACA827581
rs347027759snpC/Tintron-variant?TAIR104:10206892AATACCTGTTTGCTA[C/T]CTCTTGCCATGCTCT827581
rs347055458snpA/Gmissense?TAIR104:10208135GTCCGTGCTGTAGTA[A/G]ACAACAATAAGTTAC827581
rs347105861snpA/Gsynonymous-codon?TAIR104:10205724AAAGGTTGAAGAAAA[A/G]AATGAACCATGTCCT827581
rs347124685snpC/Tintron-variant?TAIR104:10203757ATCGGTAAGAATTTA[C/T]CCTCGTTGCTCGTCG827581
rs347141099snpA/Gmissense?TAIR104:10206264ACTGAGTGCAGCATG[A/G]CAGGGCTCGATAATT827581
rs347316475snpC/Tmissense?TAIR104:10207915GCAAATCTGGAAATC[C/T]CAATCACGGAGAATG827581
rs347320563snpA/Gintron-variant?TAIR104:10206592AATACGGATTCCGCC[A/G]AAAATACAGCAAATG827581
rs347340742snpG/Tmissense?TAIR104:10207151TTATGGCTGATCTGC[G/T]TGCAGTGAAAACTCA827581
rs347351979snpA/Gmissense?TAIR104:10206097GGCAAAATATCACCA[A/G]GCACTCGTACAAGCC827581
rs347369144snpA/Cmissense?TAIR104:10204796ATACATGGAACTTCA[A/C]GTCAATGACAGATGA827581
rs347420292snpA/Cmissense?TAIR104:10207578CATGTCTCCAAGAGA[A/C]AACAGGTCTCTAATT827581
rs347427661snpC/Tintron-variant?TAIR104:10207194GAACATACAGCAGTT[C/T]CTGGTATGGGATCTC827581
rs347441025snpG/Tutr-variant-5-prime?TAIR104:10203720TTAGCGCCTACTACA[G/T]ATACAACTGCAAAGC827581
rs347453012snpA/Tintron-variant?TAIR104:10204697GAAACCATAAGATGT[A/T]GTTCCCATTGTTAAA827581
Full records
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