Q9C9B0 · U89B1_ARATH

Variants

147350100150200250300350400450
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH001418732K>T1000Genomes
tmp_1_27785171_C_A10P>Q1000Genomes
ENSVATH0514164612K>R1000Genomes
ENSVATH0514164741G>A1000Genomes
ENSVATH1380482156P>R1000Genomes
ENSVATH0514164966V>F1000Genomes
ENSVATH1380482281I>L1000Genomes
ENSVATH1380482390D>E1000Genomes
ENSVATH05141652111I>L1000Genomes
ENSVATH05141654119S>Y1000Genomes
tmp_1_27785617_A_C159I>L1000Genomes
ENSVATH05141658167E>G1000Genomes
ENSVATH05141659171N>K1000Genomes
ENSVATH05141660175H>Q1000Genomes
ENSVATH14477574187F>Y1000Genomes
tmp_1_27785704_G_A188D>N1000Genomes
ENSVATH14477585224S>L1000Genomes
tmp_1_27785884_G_A248V>I1000Genomes
tmp_1_27785888_G_C249G>A1000Genomes
ENSVATH00141875252I>L1000Genomes
ENSVATH01533229257D>G1000Genomes
ENSVATH05141661322K>I1000Genomes
ENSVATH01533230323D>Y1000Genomes
tmp_1_27786136_G_T332G>C1000Genomes
tmp_1_27786167_T_A342L>Q1000Genomes
ENSVATH14477587359V>I1000Genomes
tmp_1_27786268_G_T376V>F1000Genomes
tmp_1_27786271_G_T377A>S1000Genomes
ENSVATH05141664391Y>F1000Genomes
ENSVATH00141882399D>E1000Genomes
ENSVATH01533232417P>S1000Genomes
ENSVATH01533234422R>P1000Genomes
ENSVATH13804829426D>E1000Genomes
tmp_1_27786430_G_A430G>R1000Genomes
ENSVATH00141886431N>K1000Genomes
ENSVATH05141666436I>V1000Genomes
ENSVATH01533236453G>R1000Genomes
ENSVATH01533239457N>K1000Genomes
tmp_1_27786517_T_A459L>I1000Genomes
ENSVATH01533240464Q>K1000Genomes
ENSVATH01533241464Q>R1000Genomes
ENSVATH05141668466V>A1000Genomes
tmp_1_27786544_A_C468S>R1000Genomes
tmp_1_27786560_A_C473K>T1000Genomes
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