Primary Site >> Pancreatic Cancer

Gene >> FBXW7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000281708
Start 152411779:152411779(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.25G>A
AA Mutation p.Gly9Ser(p.G9S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000281708
Start 152329677:152329677(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1231G>A
AA Mutation p.Gly411Ser(p.G411S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000281708
Start 152337825:152337825(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.838T>C
AA Mutation p.Phe280Leu(p.F280L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000281708
Start 152332708:152332709(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.872_873delAT
AA Mutation p.Tyr291CysfsTer25(p.Y291Cfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000281708
Start 152322987:152322987(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2018G>A
AA Mutation p.Trp673Ter(p.W673*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000281708
Start 152328320:152328321(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1304_1305dupTT
AA Mutation p.Ser436LeufsTer63(p.S436Lfs*63)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript