Primary Site >> Stomach Cancer

Gene >> PSMB4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000290541
Start 151400531:151400531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.437C>T
AA Mutation p.Ser146Leu(p.S146L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000290541
Start 151401629:151401629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.781A>G
AA Mutation p.Ser261Gly(p.S261G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000290541
Start 151400174:151400174(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.334C>A
AA Mutation p.Leu112Ile(p.L112I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000290541
Start 151400797:151400797(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.528C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000290541
Start 151400002:151400002(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.162C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000290541
Start 151399692:151399692(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.105G>A
Mutation Classification Silent
Feature Type Transcript