Primary Site >> Stomach Cancer

Gene >> EPHX3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000221730
Start 15231350:15231350(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748210176
CDS Mutation c.376G>A
AA Mutation p.Val126Ile(p.V126I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000221730
Start 15232036:15232036(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.176G>A
AA Mutation p.Arg59His(p.R59H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000221730
Start 15232078:15232078(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.134C>T
AA Mutation p.Thr45Met(p.T45M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000221730
Start 15231792:15231792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.313G>A
AA Mutation p.Gly105Ser(p.G105S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000221730
Start 15232020:15232020(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753002623
CDS Mutation c.192C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000221730
Start 15232047:15232047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.165C>T
Mutation Classification Silent
Feature Type Transcript