Primary Site >> Esophagus Cancer

Gene >> PHLPP1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262719
Start 62972558:62972558(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765622042
CDS Mutation c.3605G>A
AA Mutation p.Arg1202His(p.R1202H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262719
Start 62895049:62895049(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2105A>G
AA Mutation p.His702Arg(p.H702R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000262719
Start 62979140:62979140(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4863G>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000262719
Start 62978672:62978672(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377385853
CDS Mutation c.4395C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000262719
Start 62972653:62972654(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3706dupA
AA Mutation p.Thr1236AsnfsTer38(p.T1236Nfs*38)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript