Primary Site >> Stomach Cancer

Gene >> HAVCR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000339252
Start 157055249:157055249(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.331G>A
AA Mutation p.Gly111Arg(p.G111R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000339252
Start 157052593:157052593(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.441C>A
AA Mutation p.Ser147Arg(p.S147R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000339252
Start 157052505:157052505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.529A>G
AA Mutation p.Thr177Ala(p.T177A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000339252
Start 157055237:157055237(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.343G>A
AA Mutation p.Asp115Asn(p.D115N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000339252
Start 157052560:157052572(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.462_474delGACTGTTCCAATG
AA Mutation p.Thr155ArgfsTer12(p.T155Rfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript