Primary Site >> Pancreatic Cancer

Gene >> GCM2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379491
Start 10877220:10877220(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.263C>T
AA Mutation p.Thr88Ile(p.T88I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000379491
Start 10877283:10877283(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200953294
CDS Mutation c.200G>A
AA Mutation p.Arg67His(p.R67H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000379491
Start 10874202:10874202(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1314G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000379491
Start 10874370:10874370(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1146G>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000379491
Start 10881775:10881775(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.19C>T
AA Mutation p.Gln7Ter(p.Q7*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript