Primary Site >> Stomach Cancer

Gene >> PTTG1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000352433
Start 160427852:160427852(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777537997
CDS Mutation c.508C>T
AA Mutation p.Pro170Ser(p.P170S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000352433
Start 160427840:160427840(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.496C>T
AA Mutation p.Pro166Ser(p.P166S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000352433
Start 160428654:160428654(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.582A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000352433
Start 160422794:160422794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.177T>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000352433
Start 160427830:160427830(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.491delC
AA Mutation p.Pro164LeufsTer4(p.P164Lfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript