Q9M0R4 · ATL37_ARATH

Variants

135750100150200250300350
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH113540993I>L1000Genomes
ENSVATH065846967D>Y1000Genomes
ENSVATH065846979S>G1000Genomes
ENSVATH1135410018L>V1000Genomes
tmp_4_5815906_C_T20L>F1000Genomes
ENSVATH0048179928Y>H1000Genomes
tmp_4_5815939_T_A31C>S1000Genomes
tmp_4_5815946_A_C33Q>P1000Genomes
ENSVATH1410281738A>P1000Genomes
ENSVATH1135410143K>N1000Genomes
ENSVATH0658469846E>A1000Genomes
ENSVATH0658469946E>D1000Genomes
tmp_4_5815996_A_G50I>V1000Genomes
ENSVATH0275739878T>A1000Genomes
ENSVATH0275739878T>P1000Genomes
ENSVATH1135410278T>R1000Genomes
tmp_4_5816093_A_G82E>G1000Genomes
ENSVATH0048180183V>M1000Genomes
ENSVATH0658470198E>K1000Genomes
ENSVATH02757400117G>R1000Genomes
ENSVATH06584703125C>R1000Genomes
ENSVATH00481803132P>S1000Genomes
ENSVATH00481804149D>E1000Genomes
ENSVATH11354103159P>L1000Genomes
tmp_4_5816348_T_A167L>Q1000Genomes
ENSVATH08315242171D>A1000Genomes
ENSVATH08315242171D>V1000Genomes
ENSVATH02757403175H>N1000Genomes
tmp_4_5816402_C_G185A>G1000Genomes
ENSVATH02757406193P>L1000Genomes
ENSVATH11354104230L>R1000Genomes
tmp_4_5816554_C_A236H>N1000Genomes
ENSVATH06584708252F>C1000Genomes
ENSVATH06584708252F>Y1000Genomes
ENSVATH00481805257P>S1000Genomes
tmp_4_5816633_G_A262R>K1000Genomes
ENSVATH00481806274H>R1000Genomes
tmp_4_5816668_C_T274H>Y1000Genomes
tmp_4_5816740_G_A298G>S1000Genomes
tmp_4_5816771_G_A308R>Q1000Genomes
ENSVATH06584711309A>V1000Genomes
tmp_4_5816791_T_A,G315S>A1000Genomes
tmp_4_5816791_T_A,G315S>T1000Genomes
tmp_4_5816809_G_A321A>T1000Genomes
ENSVATH00481808323V>A1000Genomes
tmp_4_5816818_C_T324R>W1000Genomes
ENSVATH00481809326T>I1000Genomes
ENSVATH00481810329R>T1000Genomes
tmp_4_5816848_C_G334R>G1000Genomes
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