Primary Site >> Stomach Cancer

Gene >> PICK1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356976
Start 38074966:38074966(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1082A>C
AA Mutation p.Glu361Ala(p.E361A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356976
Start 38073806:38073806(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.817G>A
AA Mutation p.Glu273Lys(p.E273K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356976
Start 38074373:38074373(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.901C>T
AA Mutation p.Arg301Cys(p.R301C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356976
Start 38074935:38074935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1051G>A
AA Mutation p.Val351Met(p.V351M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000356976
Start 38074367:38074367(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.895C>T
AA Mutation p.Arg299Cys(p.R299C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000356976
Start 38074943:38074943(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1059G>A
Mutation Classification Silent
Feature Type Transcript