O23614 · CTPA2_ARATH

Variants

151550100150200250300350400450500
GAVLISTCMDNEQRKHFYWPd*GAVLISTCMDNEQRKHFYWPd*
Variant
ID(s)
Position(s)ChangeDescriptionClinical
significance
Provenance
tmp_4_9869531_A_T30L>M1000Genomes
tmp_4_9869526_C_A31W>C1000Genomes
ENSVATH1194313733K>T1000Genomes
ENSVATH1194313535P>A1000Genomes
tmp_4_9869503_G_A39S>L1000Genomes
ENSVATH1194311443K>N1000Genomes
ENSVATH1194311344F>C1000Genomes
ENSVATH1423994847A>V1000Genomes
ENSVATH0286830950R>L1000Genomes
ENSVATH1194311253I>N1000Genomes
ENSVATH0670684358A>V1000Genomes
ENSVATH1194311059A>T1000Genomes
tmp_4_9869429_C_T64V>M1000Genomes
ENSVATH1194310874I>V1000Genomes
ENSVATH1194310787M>L1000Genomes
ENSVATH1194310690S>P1000Genomes
tmp_4_9869339_A_G94F>L1000Genomes
ENSVATH06706841100V>A1000Genomes
tmp_4_9869317_G_C101A>G1000Genomes
tmp_4_9869312_C_G103V>L1000Genomes
ENSVATH00517622163L>I1000Genomes
tmp_4_9869009_C_T172E>K1000Genomes
ENSVATH14239946186D>G1000Genomes
tmp_4_9868855_T_C197K>R1000Genomes
ENSVATH11943020219P>L1000Genomes
ENSVATH11943019220T>A1000Genomes
ENSVATH11943016246L>S1000Genomes
ENSVATH14239913278A>T1000Genomes
ENSVATH11943000282A>T1000Genomes
ENSVATH11942999289T>M1000Genomes
tmp_4_9868378_G_T291L>I1000Genomes
ENSVATH06706831295T>M1000Genomes
ENSVATH00517619297E>D1000Genomes
tmp_4_9868244_G_A312P>S1000Genomes
tmp_4_9868030_C_T353V>I1000Genomes
ENSVATH11942942373F>L1000Genomes
ENSVATH11942936402A>S1000Genomes
tmp_4_9867711_T_C403T>A1000Genomes
ENSVATH06706817413K>R1000Genomes
tmp_4_9867519_C_T434V>I1000Genomes
tmp_4_9867390_C_A450E>*1000Genomes
tmp_4_9867357_C_T461V>I1000Genomes
tmp_4_9867333_G_A469H>Y1000Genomes
ENSVATH11942869488P>S1000Genomes
tmp_4_9867140_T_G499K>T1000Genomes
tmp_4_9867105_G_T511L>I1000Genomes
tmp_4_9867104_A_G511L>P1000Genomes
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