Q93WK5 · APRR7_ARATH

Variants

1727100200300400500600700
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_5_641442_C_T7G>E1000Genomes
tmp_5_641409_T_A18K>M1000Genomes
ENSVATH0691123640T>I1000Genomes
ENSVATH0301123047V>G1000Genomes
ENSVATH0060267263T>S1000Genomes
ENSVATH1051273065A>T1000Genomes
tmp_5_640413_G_A215T>I1000Genomes
ENSVATH13888847216Q>E1000Genomes
ENSVATH06911224245N>T1000Genomes
tmp_5_639881_G_A295P>L1000Genomes
ENSVATH00602665301A>V1000Genomes
ENSVATH13888845313D>N1000Genomes
ENSVATH00602664333D>N1000Genomes
tmp_5_639664_C_T335A>T1000Genomes
ENSVATH06911214339K>R1000Genomes
tmp_5_639644_T_A341E>D1000Genomes
ENSVATH03011223342P>L1000Genomes
ENSVATH00602663346T>I1000Genomes
tmp_5_639592_T_C359S>G1000Genomes
tmp_5_639555_G_A371P>L1000Genomes
tmp_5_639546_A_T374L>H1000Genomes
tmp_5_639499_A_G390S>P1000Genomes
ENSVATH00602662408P>L1000Genomes
ENSVATH06911212413K>E1000Genomes
tmp_5_639427_T_G414T>P1000Genomes
tmp_5_639422_T_G415L>F1000Genomes
tmp_5_639379_G_T430H>N1000Genomes
tmp_5_639366_C_T434S>N1000Genomes
tmp_5_639158_T_C471N>S1000Genomes
ENSVATH00602660478G>E1000Genomes
ENSVATH06911204497T>N1000Genomes
ENSVATH06911203498E>V1000Genomes
tmp_5_639027_G_T515H>N1000Genomes
ENSVATH00602658572L>H1000Genomes
tmp_5_638843_G_A576A>V1000Genomes
ENSVATH06911201589N>I1000Genomes
ENSVATH03011221592N>T1000Genomes
ENSVATH03011220594T>M1000Genomes
ENSVATH06911200601T>A1000Genomes
tmp_5_638689_C_T627M>I1000Genomes
ENSVATH00602656632M>K1000Genomes
ENSVATH13888788657S>N1000Genomes
tmp_5_638558_G_A671A>V1000Genomes
tmp_5_638507_T_A688K>M1000Genomes
tmp_5_638321_T_G,C716T>A1000Genomes
tmp_5_638321_T_G,C716T>P1000Genomes
ENSVATH06911193721I>R1000Genomes
ENSVATH00602655723N>I1000Genomes
tmp_5_638298_G_T723N>K1000Genomes
tmp_5_638296_A_T724I>N1000Genomes
ENSVATH13888787725E>V1000Genomes
tmp_5_638286_G_T727S>R1000Genomes
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