Primary Site >> Liver Cancer

Gene >> PSMD1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000308696
Start 231163651:231163651(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761435030
CDS Mutation c.2405A>G
AA Mutation p.Tyr802Cys(p.Y802C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000308696
Start 231072223:231072223(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.689G>T
AA Mutation p.Ser230Ile(p.S230I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000308696
Start 231072225:231072225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.691G>T
AA Mutation p.Asp231Tyr(p.D231Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000308696
Start 231080216:231080216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1315G>A
AA Mutation p.Glu439Lys(p.E439K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000308696
Start 231062553:231062553(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.182C>T
AA Mutation p.Ala61Val(p.A61V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000308696
Start 231072360:231072360(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.826G>T
AA Mutation p.Ala276Ser(p.A276S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000308696
Start 231066997:231066997(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.396C>T
Mutation Classification Silent
Feature Type Transcript