Primary Site >> Pancreatic Cancer

Gene >> CHD4

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000357008
Start 6601289:6601289(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.799G>A
AA Mutation p.Gly267Ser(p.G267S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6581733:6581733(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4597C>A
AA Mutation p.Pro1533Thr(p.P1533T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6591492:6591492(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3314G>A
AA Mutation p.Arg1105Gln(p.R1105Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000357008
Start 6592751:6592751(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2719A>C
AA Mutation p.Asn907His(p.N907H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000357008
Start 6598055:6598055(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1731G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000357008
Start 6578121:6578121(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5136G>A
AA Mutation p.Trp1712Ter(p.W1712*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000357008
Start 6583379:6583379(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3880-1G>T
Mutation Classification Splice_Site
Feature Type Transcript