Primary Site >> Pancreatic Cancer

Gene >> SBF2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000256190
Start 9832280:9832280(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3596G>A
AA Mutation p.Gly1199Glu(p.G1199E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000256190
Start 9852689:9852689(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143887793
CDS Mutation c.2597C>T
AA Mutation p.Pro866Leu(p.P866L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000256190
Start 10029828:10029828(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.450C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000256190
Start 10042883:10042883(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.240C>T
Mutation Classification Silent
Feature Type Transcript