Q9FY46 · SUT41_ARATH

Variants

168550100150200250300350400450500550600650200400600

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_5_4359462_T_C10D>G1000Genomes
tmp_5_4359423_G_A23S>F1000Genomes
tmp_5_4359297_G_A65A>V1000Genomes
ENSVATH0696326169R>C1000Genomes
tmp_5_4359277_G_T72L>I1000Genomes
tmp_5_4358727_C_T139A>T1000Genomes
ENSVATH03053693167A>T1000Genomes
tmp_5_4358642_G_A167A>V1000Genomes
tmp_5_4358638_A_T168D>E1000Genomes
tmp_5_4358636_G_A169T>M1000Genomes
tmp_5_4358606_A_G179I>T1000Genomes
tmp_5_4358597_G_C182A>G1000Genomes
ENSVATH00620522232S>G1000Genomes
tmp_5_4357836_A_G255W>R1000Genomes
tmp_5_4357681_G_C277A>G1000Genomes
tmp_5_4356961_T_C377I>M1000Genomes
ENSVATH03053689388T>A1000Genomes
ENSVATH10732443516I>V1000Genomes
tmp_5_4355973_T_C526N>D1000Genomes
tmp_5_4355940_T_C537I>V1000Genomes
tmp_5_4355771_C_T567D>N1000Genomes
ENSVATH03053687635V>I1000Genomes
tmp_5_4355508_C_A654K>N1000Genomes
ENSVATH10732442665S>R1000Genomes
ENSVATH03053686679P>T1000Genomes
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