Q8L860 · TOL9_ARATH

Variants

167550100150200250300350400450500550600650
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH1432815011S>N1000Genomes
ENSVATH1432815128M>I1000Genomes
tmp_4_15800782_C_A132R>S1000Genomes
tmp_4_15800893_G_T169G>C1000Genomes
tmp_4_15800903_T_C172V>A1000Genomes
ENSVATH12355829193K>R1000Genomes
tmp_4_15802045_G_T251A>S1000Genomes
tmp_4_15802157_T_G288L>R1000Genomes
tmp_4_15802542_C_T310S>L1000Genomes
tmp_4_15802544_A_C311S>R1000Genomes
ENSVATH12355832314N>K1000Genomes
ENSVATH02951657332A>V1000Genomes
tmp_4_15802659_T_G349V>G1000Genomes
ENSVATH12355833354P>S1000Genomes
tmp_4_15802746_C_A378P>Q1000Genomes
ENSVATH00549036443P>L1000Genomes
ENSVATH00549037446Q>E1000Genomes
tmp_4_15802960_G_C449Q>H1000Genomes
ENSVATH14328180454A>T1000Genomes
ENSVATH00549039467A>T1000Genomes
ENSVATH06814052489T>N1000Genomes
ENSVATH00549043513P>Q1000Genomes
ENSVATH00549045534I>N1000Genomes
ENSVATH06814054534I>V1000Genomes
tmp_4_15803432_A_C543N>T1000Genomes
ENSVATH06814055554A>T1000Genomes
ENSVATH00549046555L>F1000Genomes
ENSVATH00549046555L>I1000Genomes
tmp_4_15803483_A_C,T560Q>L1000Genomes
tmp_4_15803483_A_C,T560Q>P1000Genomes
tmp_4_15803541_A_C579Q>H1000Genomes
tmp_4_15803672_A_G623D>G1000Genomes
tmp_4_15803681_C_T626S>L1000Genomes
tmp_4_15803689_G_A629V>I1000Genomes
ENSVATH00549047630A>P1000Genomes
ENSVATH14328182639L>R1000Genomes
tmp_4_15803728_A_G642M>V1000Genomes
tmp_4_15803829_G_T675M>I1000Genomes
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