Primary Site >> Stomach Cancer

Gene >> FCGR2A

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000271450
Start 161506423:161506423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.196C>T
AA Mutation p.Arg66Cys(p.R66C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000271450
Start 161518053:161518053(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376020188
CDS Mutation c.859G>A
AA Mutation p.Gly287Ser(p.G287S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000271450
Start 161506535:161506535(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368359610
CDS Mutation c.308C>T
AA Mutation p.Thr103Met(p.T103M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000271450
Start 161510036:161510036(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765336574
CDS Mutation c.581C>T
AA Mutation p.Thr194Met(p.T194M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000271450
Start 161506480:161506480(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.253C>T
AA Mutation p.His85Tyr(p.H85Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000271450
Start 161510940:161510940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.726G>A
Mutation Classification Silent
Feature Type Transcript