Primary Site >> Pancreatic Cancer

Gene >> APC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112841068:112841068(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5474A>G
AA Mutation p.Asp1825Gly(p.D1825G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112775678:112775678(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.472T>C
AA Mutation p.Tyr158His(p.Y158H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112792488:112792488(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs587779805
CDS Mutation c.688C>T
AA Mutation p.Arg230Cys(p.R230C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112840432:112840432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4838C>A
AA Mutation p.Pro1613His(p.P1613H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112839349:112839349(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3755C>A
AA Mutation p.Ser1252Tyr(p.S1252Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000257430
Start 112827194:112827194(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs137854580
CDS Mutation c.1495C>T
AA Mutation p.Arg499Ter(p.R499*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript