Primary Site >> Stomach Cancer

Gene >> CYP2C18

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000285979
Start 94688149:94688149(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750028305
CDS Mutation c.356G>A
AA Mutation p.Arg119Lys(p.R119K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000285979
Start 94724480:94724480(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1096C>A
AA Mutation p.Leu366Met(p.L366M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000285979
Start 94733328:94733328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1181T>C
AA Mutation p.Val394Ala(p.V394A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000285979
Start 94687786:94687786(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.185G>A
AA Mutation p.Gly62Asp(p.G62D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000285979
Start 94735300:94735300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1329G>T
AA Mutation p.Met443Ile(p.M443I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000285979
Start 94724521:94724521(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1137C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000285979
Start 94695052:94695053(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.617_618insTACACACAGTTACTTTAACTACTCATTATATA
AA Mutation p.Arg206SerfsTer14(p.R206Sfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript