At2g40770
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346462761snpA/Gintron-variant?TAIR102:17015256CCACGTAAACTTCTT[A/G]ATAGTAACACAGATA818674
rs346500732snpA/Gmissense?TAIR102:17015437CATCTAACTCGTCCC[A/G]GCCCAAAGCATAGAT818674
rs346550151snpG/Tmissense?TAIR102:17016867TTAAGCACTAACCGA[G/T]AACTCTCTCTGGAGG818674
rs346560717snpC/Gmissense?TAIR102:17017322CAAACTATATCCAGA[C/G]TTTTGCATTCTTCAT818674
rs346593697snpA/Gmissense?TAIR102:17016508ACGTCTGCAGATGAA[A/G]TTTCATGCCATGTAT818674
rs346679531snpC/Tintron-variant?TAIR102:17018017CAAGTTGGATAGAAA[C/T]TTAAGCAGCCAGTAC818674
rs346682826snpA/Tmissense?TAIR102:17014690TCAGTCATAGCAAAA[A/T]AGCCTGTGTGAACAA818674
rs346694171snpC/Tsynonymous-codon?TAIR102:17016875TAACCGAGAACTCTC[C/T]CTGGAGGAGCTTGAA818674
rs346860998snpC/Tintron-variant?TAIR102:17019161CGTGTATGGCTACAA[C/T]ATGACAGATGAAAGA818674
rs346900132snpC/Gsynonymous-codon?TAIR102:17019380GATGGGAGAGGCAGT[C/G]ACTTGTAGAAGTTCA818674
rs346981752snpA/Cmissense?TAIR102:17020339TCTCGCTGAACCATC[A/C]AATAAGCTGCCCGTC818674
rs347052428snpC/Tmissense?TAIR102:17020388CTGGGAGCAAATCAG[C/T]TATGTCATCTCCAAG818674
rs347107867snpA/Gsynonymous-codon?TAIR102:17021229CTCAGCTTCGTCGCC[A/G]GGTAATTGATTTCTA818674
rs347167623snpA/Gmissense?TAIR102:17020652ATGTCATTACCTCTG[A/G]CCTCAACCAAGACAT818674
rs347190516snpC/Tmissense?TAIR102:17020252GCAGAGTCAAGGAAT[C/T]CCACGGAGATAGACA818674
rs347227383snpC/Tsynonymous-codon?TAIR102:17013742TTGATCTTGATTCTT[C/T]GTATTCCTGCTGCTA818674
rs347227793snpA/Tsynonymous-codon?TAIR102:17020398ATCAGCTATGTCATC[A/T]CCAAGCATTGCATCC818674
rs347239363snpG/Tsynonymous-codon?TAIR102:17020001ACCAGCAAGGATACC[G/T]CCCTGAATTCGAGGT818674
rs347253975snpA/Tintron-variant?TAIR102:17015120TTTTCCAGCGATCCA[A/T]AGTCTCACAAAAAGG818674
rs347280169snpC/Tsynonymous-codon?TAIR102:17013724TTTTAGTGTCAAGAA[C/T]TGTTGATCTTGATTC818674
rs347292105snpA/Gintron-variant?TAIR102:17019817ACGAAACGCATGAGA[A/G]ATATTAGAGGTAGAC818674
rs347302199snpG/Tmissense?TAIR102:17014980CTGTTTCATGTATTG[G/T]TGAGGAAAGATCTGG818674
rs347327566snpA/Tsynonymous-codon?TAIR102:17014009TTCCGCAGCTGGATT[A/T]AGAAGTGGCTCCACC818674
rs347377152snpA/Cintron-variant?TAIR102:17014435AGCTTCAATCTACCC[A/C]CAAAACAATAGATGA818674
rs347377330snpC/Tsynonymous-codon?TAIR102:17020407GTCATCTCCAAGCAT[C/T]GCATCCGTCCTGAAT818674
rs347409571snpC/Tutr-variant-3-prime?TAIR102:17013385AATAAAAGAGCTTAT[C/T]CTTTGCCTAACCTAC818674