Primary Site >> Stomach Cancer

Gene >> NCF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367535
Start 183565769:183565769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.935C>A
AA Mutation p.Ser312Tyr(p.S312Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367535
Start 183563293:183563293(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1192G>A
AA Mutation p.Asp398Asn(p.D398N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000367535
Start 183565765:183565765(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs556389548
CDS Mutation c.939G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000367535
Start 183569162:183569162(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.693G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000367535
Start 183590285:183590285(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.45G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000367535
Start 183590224:183590224(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.106delC
AA Mutation p.His36ThrfsTer15(p.H36Tfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript