Primary Site >> Pancreatic Cancer

Gene >> PHIP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 78946066:78946066(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4565C>T
AA Mutation p.Ser1522Phe(p.S1522F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000275034
Start 79002085:79002085(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1693C>T
AA Mutation p.Leu565Phe(p.L565F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000275034
Start 78940825:78940825(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5334T>C
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000275034
Start 78961698:78961698(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3648G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000275034
Start 78982964:78982964(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2691G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000275034
Start 79015178:79015178(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1428G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000275034
Start 78946261:78946261(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4371-1G>T
Mutation Classification Splice_Site
Feature Type Transcript