A0A1P8ASU8 · A0A1P8ASU8_ARATH

Variants

120020406080100120140160180200
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH0133001611P>S1000Genomes
ENSVATH0133001515S>F1000Genomes
ENSVATH0133001515S>Y1000Genomes
ENSVATH0133001421N>D1000Genomes
tmp_1_18366478_C_T33V>I1000Genomes
ENSVATH1346690240T>N1000Genomes
tmp_1_18366454_G_A41L>F1000Genomes
ENSVATH0491650256S>F1000Genomes
ENSVATH1427164657G>R1000Genomes
tmp_1_18366396_C_T60C>Y1000Genomes
ENSVATH1427164563A>S1000Genomes
ENSVATH1346690166E>D1000Genomes
ENSVATH0491649970D>V1000Genomes
tmp_1_18366363_T_C71H>R1000Genomes
ENSVATH0008995872L>R1000Genomes
ENSVATH0008995776I>V1000Genomes
ENSVATH1346690083S>T1000Genomes
ENSVATH0133001290T>S1000Genomes
tmp_1_18366282_T_G98E>A1000Genomes
tmp_1_18366161_G_C99A>G1000Genomes
tmp_1_18366159_G_T,A100H>N1000Genomes
tmp_1_18366159_G_T,A100H>Y1000Genomes
tmp_1_18366156_C_T101E>K1000Genomes
ENSVATH13466898106E>K1000Genomes
tmp_1_18365996_G_T126L>M1000Genomes
ENSVATH13466895134S>L1000Genomes
ENSVATH01330002139M>R1000Genomes
tmp_1_18365944_C_T143R>K1000Genomes
ENSVATH04916488145T>M1000Genomes
ENSVATH04916487149K>T1000Genomes
ENSVATH14271593162D>N1000Genomes
ENSVATH01330000166A>T1000Genomes
ENSVATH00089954170Y>H1000Genomes
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