Primary Site >> Pancreatic Cancer

Gene >> NF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358273
Start 31334897:31334897(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5872C>T
AA Mutation p.Arg1958Cys(p.R1958C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000358273
Start 31334939:31334939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5914A>G
AA Mutation p.Thr1972Ala(p.T1972A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000358273
Start 31229960:31229960(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2976G>A
AA Mutation p.Met992Ile(p.M992I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000358273
Start 31249071:31249071(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4062C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000358273
Start 31338100:31338100(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6780T>G
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000358273
Start 31159031:31159032(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.233dupA
AA Mutation p.Asn78LysfsTer29(p.N78Kfs*29)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript