A0A1P8B8N5 · A0A1P8B8N5_ARATH

Variants

121720406080100120140160180200
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_4_13005080_G_T9A>D1000Genomes
tmp_4_13005051_G_A19H>Y1000Genomes
tmp_4_13004620_T_G86N>H1000Genomes
ENSVATH0292302596T>K1000Genomes
tmp_4_13004571_A_T102L>H1000Genomes
tmp_4_13004560_T_A106T>S1000Genomes
ENSVATH12220356117T>I1000Genomes
tmp_4_13004421_A_C121F>L1000Genomes
tmp_4_13004402_A_T128F>I1000Genomes
ENSVATH14295110158S>F1000Genomes
ENSVATH06773224173I>F1000Genomes
tmp_4_13004154_C_T181M>I1000Genomes
tmp_4_13004140_C_T186S>N1000Genomes
ENSVATH06773223191K>E1000Genomes
tmp_4_13004102_C_A199D>Y1000Genomes
ENSVATH06773222209Q>*1000Genomes
ENSVATH02923022214Q>K1000Genomes
ENSVATH00537550216I>N1000Genomes
ENSVATH00537550216I>S1000Genomes
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