At1g11740
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346425017snpG/Tmissense?TAIR101:3963653TTCTTGGAGCTCTTC[G/T]TGGTAAAGACTAAAG837718
rs346460674snpA/Gintron-variant?TAIR101:3964448GCCAAATTTAAATCC[A/G]AATAACAACAACACA837718
rs346623787snpA/Gintron-variant?TAIR101:3964424TTGTTCCTCAACAAT[A/G]TGTATTTTGCCAAAT837718
rs346628382snpC/Tintron-variant?TAIR101:3965351AACCAAACCAAACCA[C/T]ATAAATTTGATAACC837718
rs346684110snpA/Gintron-variant?TAIR101:3964241GGACTTGTAGCCCCT[A/G]AACTGTGGTTAATAG837718
rs346709024snpA/Gsynonymous-codon?TAIR101:3965082GTGCACGTCATGTTG[A/G]TCTTCCATTGCAGCT837718
rs346871946snpC/Tmissense?TAIR101:3965108CAGCTAATAGATGTT[C/T]TGGACTTGAGAGCGG837718
rs346896918snpC/Gmissense?TAIR101:3966041ACAAGCTAGATTGAC[C/G]ACAAAAGCCAGCTAT837718
rs347217775snpA/Gintron-variant?TAIR101:3964301GATTAATTATTCATG[A/G]GTGACGAGTACTTTG837718
rs347440119snpC/Tsynonymous-codon?TAIR101:3965022AGAAGGCGTTGAAAA[C/T]GATGGACGTGAACTT837718
rs347450469snpA/Gintron-variant?TAIR101:3965532TTAAAATAAATTTGA[A/G]TAATGTCCAAGAATG837718
rs347454021snpG/Tmissense?TAIR101:3965875CGCAAACCCTGCTCT[G/T]TTCCGACTTTTCTTG837718
Full records
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