Primary Site >> Pancreatic Cancer

Gene >> LATS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000382592
Start 20988156:20988156(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1624C>A
AA Mutation p.Gln542Lys(p.Q542K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000382592
Start 20988157:20988157(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754558907
CDS Mutation c.1623G>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000382592
Start 20988685:20988685(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1095C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000382592
Start 20975010:20975010(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3127C>T
AA Mutation p.Arg1043Ter(p.R1043*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript