P42774 · GBF1_ARATH

Variants

131520406080100120140160180200220240260280300100200300

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_4_17311411_A_T48F>I1000Genomes
ENSVATH0683807461M>I1000Genomes
ENSVATH0055567789A>T1000Genomes
tmp_4_17311167_C_T93M>I1000Genomes
ENSVATH12440653104K>N1000Genomes
ENSVATH06838071111A>V1000Genomes
ENSVATH06838070124A>V1000Genomes
tmp_4_17310917_T_A137D>V1000Genomes
tmp_4_17310904_A_C141H>Q1000Genomes
ENSVATH06838065155D>A1000Genomes
tmp_4_17310679_C_T162E>K1000Genomes
ENSVATH06838062163Q>H1000Genomes
ENSVATH06838061164G>D1000Genomes
tmp_4_17310666_A_G166I>T1000Genomes
tmp_4_17310526_G_A184T>I1000Genomes
ENSVATH02967353189G>A1000Genomes
tmp_4_17310499_A_G193M>T1000Genomes
ENSVATH06838059213A>S1000Genomes
ENSVATH06838057279K>N1000Genomes
ENSVATH12440614280S>F1000Genomes
tmp_4_17309938_T_C287D>G1000Genomes
tmp_4_17309915_C_G295A>P1000Genomes
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