Primary Site >> Pancreatic Cancer

Gene >> SST

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000287641
Start 187669162:187669162(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.254A>C
AA Mutation p.Glu85Ala(p.E85A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000287641
Start 187669226:187669226(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.190G>A
AA Mutation p.Glu64Lys(p.E64K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000287641
Start 187669134:187669134(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774344993
CDS Mutation c.282G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000287641
Start 187670211:187670211(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758745230
CDS Mutation c.81G>A
Mutation Classification Silent
Feature Type Transcript