Q9LK50 · AB26G_ARATH

Variants

168550100150200250300350400450500550600650
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_3_4250667_T_C13N>D1000Genomes
ENSVATH0032055423G>D1000Genomes
ENSVATH1390837553T>S1000Genomes
ENSVATH0582037357E>K1000Genomes
ENSVATH1064598460P>S1000Genomes
tmp_3_4250515_G_C63I>M1000Genomes
ENSVATH0582037273K>Q1000Genomes
tmp_3_4250323_T_A101D>V1000Genomes
tmp_3_4250317_T_C103Y>C1000Genomes
ENSVATH13908353162R>S1000Genomes
tmp_3_4249955_G_A202A>V1000Genomes
tmp_3_4249779_G_A217R>C1000Genomes
ENSVATH07960082225F>I1000Genomes
tmp_3_4249749_T_G227K>Q1000Genomes
tmp_3_4249489_T_C285I>V1000Genomes
ENSVATH00320550307P>L1000Genomes
ENSVATH05820366341A>T1000Genomes
ENSVATH05820365344Q>K1000Genomes
ENSVATH00320549355L>F1000Genomes
ENSVATH05820364375R>S1000Genomes
tmp_3_4249133_A_T380L>M1000Genomes
tmp_3_4249129_T_G381E>A1000Genomes
tmp_3_4249067_T_A402I>F1000Genomes
ENSVATH02138877414D>N1000Genomes
tmp_3_4248904_G_A456T>I1000Genomes
tmp_3_4248760_C_A476W>C1000Genomes
tmp_3_4248717_C_T491E>K1000Genomes
tmp_3_4248634_C_T518M>I1000Genomes
tmp_3_4248611_G_A526T>I1000Genomes
tmp_3_4248562_G_C542I>M1000Genomes
ENSVATH00320547649I>V1000Genomes
ENSVATH13908347673Y>F1000Genomes
tmp_3_4247982_T_A682I>F1000Genomes
tmp_3_4247976_G_C684H>D1000Genomes
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