Primary Site >> Stomach Cancer

Gene >> GREM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318160
Start 240493148:240493148(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.328G>A
AA Mutation p.Val110Met(p.V110M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318160
Start 240493412:240493412(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.64C>T
AA Mutation p.Arg22Trp(p.R22W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318160
Start 240493070:240493070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.406G>A
AA Mutation p.Glu136Lys(p.E136K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000318160
Start 240492999:240492999(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.477C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000318160
Start 240493038:240493038(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.438C>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000318160
Start 240493043:240493043(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.433C>T
AA Mutation p.Arg145Ter(p.R145*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript