Primary Site >> Pancreatic Cancer

Gene >> SRGAP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355086
Start 64080345:64080345(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1383C>A
AA Mutation p.Asp461Glu(p.D461E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355086
Start 63984019:63984019(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.140A>G
AA Mutation p.Gln47Arg(p.Q47R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355086
Start 64142491:64142491(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781042705
CDS Mutation c.3077G>A
AA Mutation p.Arg1026His(p.R1026H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000355086
Start 64063054:64063054(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747601728
CDS Mutation c.939C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000355086
Start 64091372:64091372(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1533C>T
Mutation Classification Silent
Feature Type Transcript