Primary Site >> Stomach Cancer

Gene >> CYP2C19

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000371321
Start 94775489:94775489(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs17884712
CDS Mutation c.431G>A
AA Mutation p.Arg144His(p.R144H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000371321
Start 94775432:94775432(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141774245
CDS Mutation c.374G>A
AA Mutation p.Arg125His(p.R125H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000371321
Start 94842860:94842860(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs59734894
CDS Mutation c.985C>T
AA Mutation p.Arg329Cys(p.R329C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000371321
Start 94842885:94842885(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758787238
CDS Mutation c.1010C>A
AA Mutation p.Pro337His(p.P337H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000371321
Start 94775481:94775481(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.423T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000371321
Start 94781970:94781970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.792T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000371321
Start 94775435:94775436(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.378dupC
AA Mutation p.Ser127LeufsTer16(p.S127Lfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript