Primary Site >> Stomach Cancer

Gene >> PRKAR2A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265563
Start 48751613:48751613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377673441
CDS Mutation c.1187G>A
AA Mutation p.Ser396Asn(p.S396N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265563
Start 48847345:48847345(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.252G>T
AA Mutation p.Glu84Asp(p.E84D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000265563
Start 48752270:48752270(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.987C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000265563
Start 48783072:48783072(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201671205
CDS Mutation c.456C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000265563
Start 48752180:48752180(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1077C>A
AA Mutation p.Cys359Ter(p.C359*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript