Q9LF79 · ACA8_ARATH

Variants

110741002003004005006007008009001,0005001000

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_5_23116821_G_A13R>C1000Genomes
tmp_5_23116552_C_G68K>N1000Genomes
tmp_5_23115942_C_T175R>H1000Genomes
ENSVATH12819766183R>M1000Genomes
tmp_5_23115551_C_G233V>L1000Genomes
tmp_5_23114909_T_G319N>H1000Genomes
tmp_5_23114355_A_C404N>K1000Genomes
ENSVATH14636957404N>S1000Genomes
tmp_5_23113813_T_A481S>C1000Genomes
tmp_5_23113812_C_G481S>T1000Genomes
ENSVATH14636952487L>I1000Genomes
tmp_5_23113618_G_C512T>S1000Genomes
ENSVATH12819713532P>L1000Genomes
ENSVATH12819708563A>T1000Genomes
ENSVATH07437805587K>E1000Genomes
ENSVATH07437800610S>C1000Genomes
ENSVATH14636946620P>L1000Genomes
tmp_5_23112659_G_A657P>L1000Genomes
ENSVATH00738592727A>V1000Genomes
ENSVATH12819650728D>G1000Genomes
ENSVATH14636943754K>E1000Genomes
tmp_5_23111743_T_A776Q>L1000Genomes
ENSVATH07437762978P>L1000Genomes
tmp_5_23110415_T_C981K>E1000Genomes
ENSVATH074377591018T>A1000Genomes
tmp_5_23109974_T_C1057K>E1000Genomes
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