Primary Site >> Stomach Cancer

Gene >> F2RL2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000296641
Start 76617713:76617713(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.994A>C
AA Mutation p.Asn332His(p.N332H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000296641
Start 76617719:76617719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.988T>A
AA Mutation p.Tyr330Asn(p.Y330N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000296641
Start 76617661:76617661(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1046T>G
AA Mutation p.Leu349Arg(p.L349R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000296641
Start 76618184:76618184(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.523G>A
AA Mutation p.Gly175Ser(p.G175S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000296641
Start 76617848:76617848(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.859C>A
Mutation Classification Silent
Feature Type Transcript