Q9SZ11 · GPDL3_ARATH

Variants

1759100200300400500600700200400600

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH067811893G>E1000Genomes
ENSVATH0678118714G>V1000Genomes
ENSVATH0053987615V>A1000Genomes
ENSVATH0678118626H>N1000Genomes
tmp_4_13459800_T_C31K>E1000Genomes
tmp_4_13459533_C_A62D>Y1000Genomes
ENSVATH0292783864Y>F1000Genomes
ENSVATH0053987598R>S1000Genomes
ENSVATH06781182100S>A1000Genomes
ENSVATH02927836118G>R1000Genomes
ENSVATH12246691121T>I1000Genomes
ENSVATH06781179131L>W1000Genomes
tmp_4_13459166_G_C,T159T>K1000Genomes
tmp_4_13459166_G_C,T159T>R1000Genomes
ENSVATH06781174162S>N1000Genomes
ENSVATH12246690176V>F1000Genomes
tmp_4_13459103_G_C180A>G1000Genomes
ENSVATH14299794189M>I1000Genomes
ENSVATH06781172196A>V1000Genomes
ENSVATH06781171208P>S1000Genomes
ENSVATH06781169222R>S1000Genomes
tmp_4_13458956_A_T229F>Y1000Genomes
tmp_4_13458937_G_C235D>E1000Genomes
tmp_4_13458855_G_T263L>I1000Genomes
ENSVATH06781166281H>Q1000Genomes
ENSVATH06781165287D>E1000Genomes
tmp_4_13458720_G_C308H>D1000Genomes
ENSVATH14299793308H>Q1000Genomes
tmp_4_13458665_T_A326N>I1000Genomes
tmp_4_13458645_G_C333L>V1000Genomes
tmp_4_13458227_C_T410D>N1000Genomes
ENSVATH06781153446A>P1000Genomes
ENSVATH06781146458P>S1000Genomes
ENSVATH14299787519D>E1000Genomes
tmp_4_13457574_G_T527S>R1000Genomes
tmp_4_13457575_C_G527S>T1000Genomes
ENSVATH12246624554E>K1000Genomes
ENSVATH12246624554E>Q1000Genomes
ENSVATH14299786584Q>K1000Genomes
tmp_4_13457387_G_A590P>S1000Genomes
ENSVATH06781138652E>Q1000Genomes
tmp_4_13457075_C_A666L>F1000Genomes
tmp_4_13457008_G_A689P>S1000Genomes
ENSVATH09499226738T>I1000Genomes
ENSVATH02927815744L>V1000Genomes
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