Primary Site >> Stomach Cancer

Gene >> IL12B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000231228
Start 159322461:159322461(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767350741
CDS Mutation c.415C>T
AA Mutation p.Arg139Cys(p.R139C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000231228
Start 159326733:159326733(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.50C>T
AA Mutation p.Ala17Val(p.A17V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000231228
Start 159323322:159323322(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.96C>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000231228
Start 159322483:159322483(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757355295
CDS Mutation c.393C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000231228
Start 159320319:159320319(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.684C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000231228
Start 159316799:159316799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.873G>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000231228
Start 159323301:159323301(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.117G>A
Mutation Classification Silent
Feature Type Transcript