Primary Site >> Stomach Cancer

Gene >> PSMD5

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000210313
Start 120824580:120824580(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.920A>G
AA Mutation p.Gln307Arg(p.Q307R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000210313
Start 120831455:120831455(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754419425
CDS Mutation c.437T>C
AA Mutation p.Ile146Thr(p.I146T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000210313
Start 120818091:120818091(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143084016
CDS Mutation c.1330C>T
AA Mutation p.Arg444Trp(p.R444W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000210313
Start 120824528:120824528(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.972C>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000210313
Start 120833393:120833393(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.237C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000210313
Start 120833327:120833327(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.303C>A
Mutation Classification Silent
Feature Type Transcript