Q9SCS2 · CAMK5_ARATH

Variants

160150100150200250300350400450500550600
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_3_18753974_A_T48N>Y1000Genomes
tmp_3_18754103_A_C91K>Q1000Genomes
ENSVATH06287552129G>R1000Genomes
tmp_3_18754218_G_T129G>V1000Genomes
tmp_3_18754258_G_T142K>N1000Genomes
ENSVATH00413081303Y>F1000Genomes
ENSVATH06287567351P>L1000Genomes
tmp_3_18755445_G_A389R>Q1000Genomes
ENSVATH12690255411K>R1000Genomes
ENSVATH06287570427L>I1000Genomes
ENSVATH06287574451V>A1000Genomes
ENSVATH06287573451V>F1000Genomes
ENSVATH12690257455F>C1000Genomes
tmp_3_18756125_G_A510D>N1000Genomes
ENSVATH06287577523Q>K1000Genomes
tmp_3_18756251_G_A552D>N1000Genomes
tmp_3_18756369_C_T563S>F1000Genomes
tmp_3_18756368_T_A563S>T1000Genomes
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