Primary Site >> Stomach Cancer

Gene >> ERCC8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000265038
Start 60899651:60899651(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.694A>G
AA Mutation p.Lys232Glu(p.K232E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000265038
Start 60902505:60902505(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.554A>G
AA Mutation p.His185Arg(p.H185R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000265038
Start 60899685:60899685(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.660A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000265038
Start 60928954:60928954(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.83delT
AA Mutation p.Leu28TrpfsTer5(p.L28Wfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000265038
Start 60891051:60891051(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.879delA
AA Mutation p.Gly294AspfsTer2(p.G294Dfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript