Q9SZ58 · BRAT1_ARATH

Variants

145850100150200250300350400450
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_4_15441198_A_G25D>G1000Genomes
ENSVATH0680990131T>I1000Genomes
tmp_4_15441268_C_A48F>L1000Genomes
tmp_4_15441276_A_T51N>I1000Genomes
ENSVATH1234219259S>Y1000Genomes
tmp_4_15441308_T_G62S>A1000Genomes
tmp_4_15441383_G_T87G>C1000Genomes
ENSVATH0680990488G>D1000Genomes
ENSVATH0680990596N>H1000Genomes
tmp_4_15441450_G_T109G>V1000Genomes
tmp_4_15441462_C_T113S>F1000Genomes
ENSVATH06809906116G>D1000Genomes
tmp_4_15441504_A_G127N>S1000Genomes
ENSVATH14323449129V>I1000Genomes
tmp_4_15442597_T_A151F>L1000Genomes
tmp_4_15442715_A_G191S>G1000Genomes
ENSVATH06809916196K>T1000Genomes
ENSVATH06809917198E>D1000Genomes
tmp_4_15442778_C_A212L>M1000Genomes
tmp_4_15442787_C_T215R>W1000Genomes
ENSVATH00547651218V>I1000Genomes
tmp_4_15442928_A_G262N>D1000Genomes
ENSVATH06809919271K>R1000Genomes
tmp_4_15442997_C_G285L>V1000Genomes
ENSVATH02949438295R>K1000Genomes
ENSVATH06809925296A>V1000Genomes
tmp_4_15443229_A_T304M>L1000Genomes
ENSVATH12342362349E>D1000Genomes
tmp_4_15443451_A_C378N>H1000Genomes
ENSVATH06809932413Y>N1000Genomes
ENSVATH06809933425A>V1000Genomes
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