Primary Site >> Liver Cancer

Gene >> CCT3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295688
Start 156333565:156333565(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.286A>T
AA Mutation p.Thr96Ser(p.T96S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295688
Start 156311155:156311155(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758436442
CDS Mutation c.1196G>A
AA Mutation p.Arg399His(p.R399H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295688
Start 156324981:156324981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413A>G
AA Mutation p.Lys138Arg(p.K138R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295688
Start 156333597:156333597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.254G>C
AA Mutation p.Arg85Pro(p.R85P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295688
Start 156317462:156317462(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.845T>A
AA Mutation p.Ile282Asn(p.I282N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295688
Start 156317241:156317241(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.899C>A
AA Mutation p.Ala300Asp(p.A300D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000295688
Start 156317448:156317448(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.859C>T
AA Mutation p.Pro287Ser(p.P287S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000295688
Start 156320971:156320971(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.477T>C
Mutation Classification Silent
Feature Type Transcript