At4g18900
SNP - dbSNP
dbSNPTypeAllelesHetSe(het)Fxn-classGene NameAssemblyChr-posSequenceEntrez Gene
rs346510791snpC/Gintron-variant?TAIR104:10357340AATGTGTCACTAAAA[C/G]TCTTATGAATTAAAC827624
rs346600871snpA/Csynonymous-codon?TAIR104:10357263CAGAATTATACCAGC[A/C]ATTCCATTGTGTACT827624
rs346610677snpA/Tmissense?TAIR104:10359028CTTTGGGATACACTT[A/T]CGGACACTAATGTCT827624
rs346650881snpA/Tintron-variant?TAIR104:10357771ATAAGGAGTTTCGGT[A/T]TGTCCATGACTGAAT827624
rs346677508snpC/Gmissense?TAIR104:10357716TCTTAGAACTATAAA[C/G]AAGGTAGCCACACTA827624
rs346715437snpC/Tsynonymous-codon?TAIR104:10358807GCCTTCATGCATTGC[C/T]ACACACAATCCAAAT827624
rs346725106snpA/Gmissense?TAIR104:10357585CTTCAGTGGTTCGAC[A/G]TGCTACCTTGTGTAC827624
rs346787665snpG/Tintron-variant?TAIR104:10357552ACTATATTTTAATTT[G/T]AAATTGATGATATAA827624
rs346837426snpA/Cmissense?TAIR104:10358960TCTTCATTGCTTTCT[A/C]TCCGGACAATCCTTT827624
rs346852534snpC/Tintron-variant?TAIR104:10357668AACAGAAAAATGTAC[C/T]AAATGTAATCATTCT827624
rs347197832snpC/Tmissense?TAIR104:10359035ATACACTTTCGGACA[C/T]TAATGTCTCCAGCAG827624
rs347306066snpC/Gintron-variant?TAIR104:10358152ATTTCATGTATTCCA[C/G]TCTTTTGTTTTACAC827624
rs347309532snpA/Tmissense?TAIR104:10356642AAAAGCAAGAATGTT[A/T]CTTCTTCAATGGAGC827624
rs347472634snpA/Cintron-variant?TAIR104:10358117ACTGTTGTATTGGTA[A/C]ATGTTTTGTTCCATG827624
Full records
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