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Q8GXW5 · GLN15_ARATH

Variants

135350100150200250300350100200300

Filter Consequence

Filter Provenance

GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_1_17913818_A_G12D>G1000Genomes
tmp_1_17913856_T_C25W>R1000Genomes
ENSVATH0490512638R>W1000Genomes
tmp_1_17914130_T_G40L>V1000Genomes
ENSVATH1344348444V>I1000Genomes
ENSVATH0008751446N>D1000Genomes
tmp_1_17914164_C_T51P>L1000Genomes
tmp_1_17914485_C_G95Y>*1000Genomes
tmp_1_17914492_G_T98A>S1000Genomes
ENSVATH00087515106N>S1000Genomes
tmp_1_17914522_C_T108H>Y1000Genomes
tmp_1_17914540_T_C114F>L1000Genomes
tmp_1_17914829_A_G137K>E1000Genomes
tmp_1_17914832_G_A138D>N1000Genomes
ENSVATH13443536147L>R1000Genomes
ENSVATH04905145150F>Y1000Genomes
tmp_1_17915026_A_G171I>V1000Genomes
ENSVATH14261445176Y>F1000Genomes
tmp_1_17915062_G_A183G>S1000Genomes
ENSVATH14261446188G>A1000Genomes
tmp_1_17915115_T_G200F>L1000Genomes
tmp_1_17915137_A_G208I>V1000Genomes
ENSVATH13443538222E>K1000Genomes
ENSVATH01321415224I>V1000Genomes
ENSVATH04905149225T>S1000Genomes
ENSVATH13443543231I>N1000Genomes
ENSVATH13443555234F>L1000Genomes
ENSVATH13443556235D>Y1000Genomes
tmp_1_17915510_T_A242D>E1000Genomes
ENSVATH13443557246A>S1000Genomes
ENSVATH04905153254T>K1000Genomes
ENSVATH04905154255K>E1000Genomes
tmp_1_17915575_A_G264D>G1000Genomes
tmp_1_17915574_G_A264D>N1000Genomes
ENSVATH01321417268E>Q1000Genomes
ENSVATH14261447273L>F1000Genomes
tmp_1_17915629_C_T282A>V1000Genomes
tmp_1_17915649_G_A289E>K1000Genomes
ENSVATH04905155295K>R1000Genomes
ENSVATH13443558305S>C1000Genomes
tmp_1_17915792_G_A310D>N1000Genomes
ENSVATH13443559326K>I1000Genomes
tmp_1_17915865_C_T334P>L1000Genomes
ENSVATH04905158341Y>D1000Genomes
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