Q9M280 · BIC2_ARATH

Variants

111610203040506070809010011050100MKNTNLPEETKEPISPGSSHRKQNKTGTKTCFPETTVLSGRDRLKRHREEVAGKVPIPDSWGKEGLLMGWMDFSTFDAAFTSSQIVSARAALMADSGDDAGARGSRPQRLRVESSC

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH124079224T>I1000Genomes
ENSVATH003969286L>M1000Genomes
ENSVATH0039692710T>S1000Genomes
ENSVATH1240792111K>N1000Genomes
tmp_3_16074541_G_T13P>Q1000Genomes
tmp_3_16074532_G_T16P>Q1000Genomes
ENSVATH0620726817G>E1000Genomes
ENSVATH0620726720H>Y1000Genomes
ENSVATH0240989423Q>E1000Genomes
ENSVATH0039692627G>A1000Genomes
ENSVATH0039692627G>D1000Genomes
tmp_3_16074492_C_A29K>N1000Genomes
ENSVATH1434335430T>I1000Genomes
ENSVATH1434335430T>K1000Genomes
tmp_3_16074491_T_A30T>S1000Genomes
ENSVATH0039692531C>S1000Genomes
ENSVATH0240989233P>Q1000Genomes
ENSVATH0240989036T>M1000Genomes
tmp_3_16074401_T_A60S>C1000Genomes
tmp_3_16074377_T_C68M>V1000Genomes
ENSVATH1240791880F>L1000Genomes
ENSVATH1434335381T>M1000Genomes
ENSVATH0620726299D>E1000Genomes
ENSVATH02409887100A>T1000Genomes
ENSVATH02409886102A>P1000Genomes
ENSVATH02409886102A>T1000Genomes
ENSVATH14343352104G>A1000Genomes
ENSVATH06207261107P>S1000Genomes
ENSVATH06207260113E>*1000Genomes
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