Q93ZI4 · BGL10_ARATH

Variants

150850100150200250300350400450500
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_4_13864474_G_T6L>I1000Genomes
ENSVATH0054188620S>N1000Genomes
ENSVATH1226676126N>K1000Genomes
ENSVATH0678745127N>S1000Genomes
ENSVATH0678744662H>R1000Genomes
ENSVATH0836908391E>K1000Genomes
tmp_4_13863802_G_T96S>*1000Genomes
ENSVATH06787439107I>T1000Genomes
ENSVATH06787438109N>T1000Genomes
tmp_4_13863517_T_G135E>D1000Genomes
tmp_4_13863466_C_G152E>D1000Genomes
ENSVATH06787432199Q>E1000Genomes
ENSVATH08369074201I>T1000Genomes
ENSVATH08369073202S>A1000Genomes
tmp_4_13863196_G_T210N>K1000Genomes
tmp_4_13863189_T_C213I>V1000Genomes
tmp_4_13863176_C_G217S>T1000Genomes
ENSVATH06787429226L>I1000Genomes
ENSVATH09501215238A>T1000Genomes
ENSVATH02932995249T>K1000Genomes
ENSVATH12266704293F>L1000Genomes
ENSVATH06787417306S>L1000Genomes
ENSVATH06787416319L>V1000Genomes
ENSVATH00541883350E>K1000Genomes
ENSVATH00541882364A>T1000Genomes
ENSVATH06787411370L>V1000Genomes
ENSVATH06787405380G>S1000Genomes
ENSVATH06787402406D>E1000Genomes
ENSVATH12266696407S>L1000Genomes
ENSVATH08369059492T>S1000Genomes
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