Primary Site >> Pancreatic Cancer

Gene >> CCT3

ID 1
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 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000295688
Start 156309247:156309247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777489338
CDS Mutation c.1590C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000295688
Start 156319006:156319006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.621C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000295688
Start 156312060:156312061(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1135dupG
AA Mutation p.Ala379GlyfsTer2(p.A379Gfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript