Q9STS6 · LBD27_ARATH

Variants

132850100150200250300
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH0246547212Q>L1000Genomes
ENSVATH1439691526Y>D1000Genomes
ENSVATH1439690426Y>F1000Genomes
ENSVATH1262315834S>R1000Genomes
ENSVATH1439690236A>G1000Genomes
ENSVATH1439689855P>A1000Genomes
ENSVATH1439689762P>L1000Genomes
tmp_3_17660820_T_C63K>R1000Genomes
tmp_3_17660691_G_C106S>C1000Genomes
ENSVATH06264254120Y>C1000Genomes
tmp_3_17660640_C_A123W>L1000Genomes
ENSVATH14396896124F>L1000Genomes
ENSVATH06264253124F>S1000Genomes
ENSVATH06264252125A>S1000Genomes
tmp_3_17660599_G_T137Q>K1000Genomes
ENSVATH06264251140R>G1000Genomes
tmp_3_17660581_G_A143P>S1000Genomes
tmp_3_17660575_T_G145N>H1000Genomes
ENSVATH02465470155H>P1000Genomes
tmp_3_17660525_C_G161E>D1000Genomes
tmp_3_17660524_G_A162L>F1000Genomes
tmp_3_17660507_A_C167N>K1000Genomes
ENSVATH14396895167N>Y1000Genomes
ENSVATH14396894185N>K1000Genomes
ENSVATH06264249196P>Q1000Genomes
tmp_3_17660417_G_T197F>L1000Genomes
ENSVATH06264248201L>F1000Genomes
ENSVATH00406690223N>S1000Genomes
ENSVATH12623132233T>A1000Genomes
ENSVATH14396893236G>D1000Genomes
tmp_3_17660273_A_C245N>K1000Genomes
ENSVATH06264247247W>S1000Genomes
tmp_3_17660230_C_T260G>R1000Genomes
ENSVATH06264245281I>M1000Genomes
tmp_3_17660142_T_C289Q>R1000Genomes
tmp_3_17660119_C_G297V>L1000Genomes
ENSVATH02465468300E>G1000Genomes
ENSVATH00406689329*>Y1000Genomes
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