Primary Site >> Stomach Cancer

Gene >> GP6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000417454
Start 55038218:55038218(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569446020
CDS Mutation c.19G>A
AA Mutation p.Ala7Thr(p.A7T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000417454
Start 55018694:55018694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.682G>A
AA Mutation p.Ala228Thr(p.A228T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000417454
Start 55032379:55032379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.85T>A
AA Mutation p.Ser29Thr(p.S29T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000417454
Start 55018687:55018687(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.689T>C
AA Mutation p.Leu230Pro(p.L230P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000417454
Start 55027801:55027801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.387C>T
Mutation Classification Silent
Feature Type Transcript