Primary Site >> Pancreatic Cancer

Gene >> THBS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000366787
Start 169223409:169223409(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2840T>G
AA Mutation p.Val947Gly(p.V947G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366787
Start 169225247:169225247(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747986144
CDS Mutation c.2671G>A
AA Mutation p.Gly891Ser(p.G891S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366787
Start 169234851:169234851(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761495769
CDS Mutation c.1534G>A
AA Mutation p.Gly512Ser(p.G512S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000366787
Start 169222287:169222287(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767991056
CDS Mutation c.3183C>T
Mutation Classification Silent
Feature Type Transcript