Primary Site >> Stomach Cancer

Gene >> HAVCR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307851
Start 157087170:157087170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.838T>C
AA Mutation p.Tyr280His(p.Y280H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000307851
Start 157106891:157106891(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765773071
CDS Mutation c.130G>A
AA Mutation p.Ala44Thr(p.A44T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000307851
Start 157106647:157106647(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.374T>C
AA Mutation p.Leu125Pro(p.L125P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000307851
Start 157108943:157108943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.41T>C
AA Mutation p.Leu14Pro(p.L14P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000307851
Start 157087141:157087141(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.867A>G
Mutation Classification Silent
Feature Type Transcript