Primary Site >> Stomach Cancer

Gene >> NCF4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000248899
Start 36867451:36867451(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778347689
CDS Mutation c.331G>A
AA Mutation p.Ala111Thr(p.A111T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000248899
Start 36877689:36877689(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.886C>T
AA Mutation p.Arg296Trp(p.R296W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000248899
Start 36877783:36877783(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367876433
CDS Mutation c.980C>T
AA Mutation p.Thr327Met(p.T327M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000248899
Start 36870447:36870447(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.375G>T
AA Mutation p.Met125Ile(p.M125I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000248899
Start 36876080:36876080(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.810G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000248899
Start 36864951:36864951(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.150A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000248899
Start 36865006:36865006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.205C>T
Mutation Classification Silent
Feature Type Transcript