Q9C5G2 · Q9C5G2_ARATH

Variants

142350100150200250300350400100200300400

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH112558125A>V1000Genomes
ENSVATH1390044745V>F1000Genomes
ENSVATH1125581152R>H1000Genomes
ENSVATH0002441954G>A1000Genomes
tmp_1_5230772_G_A56P>L1000Genomes
tmp_1_5230767_G_C58P>A1000Genomes
ENSVATH0458022977A>V1000Genomes
tmp_1_5230450_T_C111Q>R1000Genomes
ENSVATH11255810113D>E1000Genomes
tmp_1_5230433_A_G117S>P1000Genomes
ENSVATH04580227119L>F1000Genomes
ENSVATH11255809122G>E1000Genomes
tmp_1_5230266_G_A144P>L1000Genomes
tmp_1_5230232_C_A155E>D1000Genomes
tmp_1_5229980_C_T199R>K1000Genomes
tmp_1_5229596_G_T211L>M1000Genomes
tmp_1_5229582_C_A215E>D1000Genomes
ENSVATH04580215216R>L1000Genomes
ENSVATH04580214218N>I1000Genomes
ENSVATH11255761219L>W1000Genomes
tmp_1_5229566_C_T221E>K1000Genomes
tmp_1_5229357_G_T257S>R1000Genomes
tmp_1_5229350_T_C260I>V1000Genomes
ENSVATH00024413271A>T1000Genomes
ENSVATH00024412290T>S1000Genomes
ENSVATH11255755296A>V1000Genomes
ENSVATH01054095313C>R1000Genomes
ENSVATH04580206332K>R1000Genomes
tmp_1_5228713_T_G346K>Q1000Genomes
tmp_1_5228665_T_C362I>V1000Genomes
tmp_1_5228630_T_A373E>D1000Genomes
tmp_1_5228617_C_T378D>N1000Genomes
tmp_1_5228511_G_A413A>V1000Genomes
ENSVATH04580205415E>V1000Genomes
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