Primary Site >> Pancreatic Cancer

Gene >> PIK3CG

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106883077:106883077(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2674C>G
AA Mutation p.Gln892Glu(p.Q892E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868499:106868499(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.938C>T
AA Mutation p.Pro313Leu(p.P313L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868139:106868139(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771251636
CDS Mutation c.578C>T
AA Mutation p.Pro193Leu(p.P193L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106868501:106868501(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.940G>A
AA Mutation p.Ala314Thr(p.A314T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359195
Start 106872573:106872573(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187473519
CDS Mutation c.2032G>A
AA Mutation p.Ala678Thr(p.A678T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106868458:106868458(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.897C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000359195
Start 106872763:106872763(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2112C>T
Mutation Classification Silent
Feature Type Transcript