Primary Site >> Stomach Cancer

Gene >> CD69

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000228434
Start 9754652:9754652(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.426G>T
AA Mutation p.Trp142Cys(p.W142C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000228434
Start 9755117:9755117(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.332A>G
AA Mutation p.Asn111Ser(p.N111S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000228434
Start 9755165:9755165(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.284A>G
AA Mutation p.Lys95Arg(p.K95R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000228434
Start 9755159:9755159(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.290A>G
AA Mutation p.Tyr97Cys(p.Y97C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000228434
Start 9755069:9755069(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.380A>G
AA Mutation p.Lys127Arg(p.K127R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000228434
Start 9755200:9755200(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.249T>G
Mutation Classification Silent
Feature Type Transcript