Q5XF75 · EFTS_ARATH

Variants

139550100150200250300350100200300

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
ENSVATH027842652A>T1000Genomes
tmp_4_6778082_C_A6A>E1000Genomes
ENSVATH0661325016Y>F1000Genomes
ENSVATH1148745826N>K1000Genomes
ENSVATH0048928035F>L1000Genomes
ENSVATH0661325136E>G1000Genomes
ENSVATH0661325245V>L1000Genomes
ENSVATH0048928146P>S1000Genomes
ENSVATH0048928252L>P1000Genomes
ENSVATH0661325362S>N1000Genomes
tmp_4_6778252_T_A63F>I1000Genomes
ENSVATH0661325464S>C1000Genomes
ENSVATH0661325583E>G1000Genomes
tmp_4_6778504_G_T117L>F1000Genomes
tmp_4_6778512_A_T120K>I1000Genomes
tmp_4_6778518_C_T122S>L1000Genomes
tmp_4_6778562_G_A137E>K1000Genomes
ENSVATH11487508140V>F1000Genomes
ENSVATH11487508140V>I1000Genomes
tmp_4_6778577_G_A142V>I1000Genomes
ENSVATH00489285143I>V1000Genomes
ENSVATH00489288164A>G1000Genomes
ENSVATH00489289173E>D1000Genomes
ENSVATH11487539174S>N1000Genomes
tmp_4_6778774_G_T175S>I1000Genomes
tmp_4_6778777_C_T176S>L1000Genomes
tmp_4_6778792_G_C181G>A1000Genomes
ENSVATH06613259183F>Y1000Genomes
tmp_4_6778815_C_A189L>I1000Genomes
tmp_4_6779048_G_A223V>I1000Genomes
tmp_4_6779074_G_T231M>I1000Genomes
tmp_4_6779072_A_C231M>L1000Genomes
tmp_4_6779094_T_C238V>A1000Genomes
ENSVATH06613262241A>T1000Genomes
tmp_4_6779287_C_T271A>V1000Genomes
ENSVATH00489292283V>I1000Genomes
tmp_4_6779368_C_T298S>F1000Genomes
ENSVATH11487586301M>I1000Genomes
tmp_4_6779393_G_T306E>D1000Genomes
tmp_4_6779401_A_G309K>R1000Genomes
ENSVATH11487587315T>S1000Genomes
ENSVATH06613264349A>G1000Genomes
ENSVATH11487589349A>S1000Genomes
tmp_4_6779623_A_G351N>D1000Genomes
tmp_4_6779760_C_T366P>L1000Genomes
ENSVATH11487597368K>M1000Genomes
tmp_4_6779767_G_C368K>N1000Genomes
tmp_4_6779768_G_C369V>L1000Genomes
tmp_4_6779804_A_C381I>L1000Genomes
ENSVATH06613266389E>K1000Genomes
ENSVATH06613267389E>V1000Genomes
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