Primary Site >> Stomach Cancer

Gene >> TREM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000373113
Start 41159841:41159841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.433G>A
AA Mutation p.Gly145Arg(p.G145R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000373113
Start 41161400:41161400(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.254C>T
AA Mutation p.Thr85Ile(p.T85I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000373113
Start 41161600:41161600(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.54C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000373113
Start 41158991:41158991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.558G>A
Mutation Classification Silent
Feature Type Transcript