Primary Site >> Stomach Cancer

Gene >> ARPC1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000252725
Start 99388170:99388170(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.301T>G
AA Mutation p.Cys101Gly(p.C101G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000252725
Start 99388053:99388053(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.184C>T
AA Mutation p.Pro62Ser(p.P62S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000252725
Start 99391211:99391211(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.741G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000252725
Start 99391013:99391013(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.621C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000252725
Start 99388103:99388103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.234G>A
Mutation Classification Silent
Feature Type Transcript