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Q9FHE8 · P2A06_ARATH

Variants

139250100150200250300350100200300

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_5_18193194_G_A5S>F1000Genomes
ENSVATH0733868610P>S1000Genomes
ENSVATH0070870340E>K1000Genomes
ENSVATH0335662758A>D1000Genomes
ENSVATH0733868558A>T1000Genomes
ENSVATH0335662758A>V1000Genomes
tmp_5_18192969_C_A,G80R>I1000Genomes
tmp_5_18192969_C_A,G80R>T1000Genomes
ENSVATH0070870283R>W1000Genomes
ENSVATH0733868486N>D1000Genomes
ENSVATH0070870186N>K1000Genomes
ENSVATH0733868386N>S1000Genomes
ENSVATH03356625116F>Y1000Genomes
ENSVATH03356624135M>I1000Genomes
ENSVATH00708698138I>R1000Genomes
ENSVATH07338682141K>E1000Genomes
ENSVATH00708697151G>E1000Genomes
ENSVATH07338681157L>F1000Genomes
tmp_5_18192735_G_T158A>D1000Genomes
ENSVATH07338680158A>T1000Genomes
tmp_5_18192579_C_A181E>D1000Genomes
tmp_5_18192439_C_T228S>N1000Genomes
ENSVATH12532859248H>D1000Genomes
ENSVATH00708692249S>F1000Genomes
ENSVATH03356622254K>I1000Genomes
ENSVATH03356622254K>R1000Genomes
ENSVATH00708691258S>R1000Genomes
ENSVATH03356621264P>Q1000Genomes
ENSVATH07338669267A>V1000Genomes
tmp_5_18191950_T_A268E>D1000Genomes
ENSVATH00708688274L>S1000Genomes
ENSVATH03356615287T>N1000Genomes
ENSVATH14591306302V>A1000Genomes
ENSVATH00708687325H>Q1000Genomes
ENSVATH07338668335T>I1000Genomes
tmp_5_18191714_A_G347V>A1000Genomes
ENSVATH12532832372Y>H1000Genomes
ENSVATH03356613374D>V1000Genomes
ENSVATH00708685375K>E1000Genomes
ENSVATH12532831378K>R1000Genomes
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