Primary Site >> Stomach Cancer

Gene >> IFNB1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000380232
Start 21077709:21077709(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.161A>C
AA Mutation p.Lys54Thr(p.K54T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000380232
Start 21077519:21077519(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.351C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000380232
Start 21077828:21077828(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.42C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000380232
Start 21077645:21077645(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368199428
CDS Mutation c.225C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000380232
Start 21077363:21077363(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.507G>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000380232
Start 21077393:21077393(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.477C>G
AA Mutation p.Tyr159Ter(p.Y159*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript