Q9LSR9 · LRK18_ARATH

Variants

165750100150200250300350400450500550600650
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_5_24260588_G_A9W>*1000Genomes
tmp_5_24260635_G_A25E>K1000Genomes
tmp_5_24260656_G_A32G>S1000Genomes
tmp_5_24260680_G_C40V>L1000Genomes
tmp_5_24260701_C_G47L>V1000Genomes
tmp_5_24260824_G_A88A>T1000Genomes
tmp_5_24260866_G_T102A>S1000Genomes
tmp_5_24261088_G_A176D>N1000Genomes
ENSVATH07454714180L>F1000Genomes
tmp_5_24261161_G_C200G>A1000Genomes
tmp_5_24261164_C_T201T>I1000Genomes
ENSVATH07454715205V>A1000Genomes
tmp_5_24261233_T_A224M>K1000Genomes
tmp_5_24261269_T_C236V>A1000Genomes
tmp_5_24261326_G_C255S>T1000Genomes
ENSVATH07454716337K>R1000Genomes
tmp_5_24261737_G_A392R>K1000Genomes
ENSVATH14642220464K>N1000Genomes
tmp_5_24261988_G_C476G>R1000Genomes
ENSVATH03457285480D>N1000Genomes
ENSVATH07454719494T>K1000Genomes
ENSVATH03457286506G>A1000Genomes
tmp_5_24262109_C_T516T>I1000Genomes
ENSVATH12873150525A>S1000Genomes
ENSVATH12873151531T>I1000Genomes
tmp_5_24262195_A_C545K>Q1000Genomes
ENSVATH12873152551W>R1000Genomes
ENSVATH12873153558R>K1000Genomes
ENSVATH14642221562I>F1000Genomes
ENSVATH00744649574I>R1000Genomes
tmp_5_24262300_G_T580V>L1000Genomes
tmp_5_24262356_G_A598M>I1000Genomes
ENSVATH07454720607R>G1000Genomes
ENSVATH03457288613D>N1000Genomes
tmp_5_24262427_G_A622G>E1000Genomes
ENSVATH12873154624V>I1000Genomes
tmp_5_24262438_C_T626P>S1000Genomes
ENSVATH07454721651I>F1000Genomes
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