Primary Site >> Stomach Cancer

Gene >> PABPC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318607
Start 100713175:100713175(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.650C>T
AA Mutation p.Ala217Val(p.A217V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318607
Start 100706932:100706932(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763825223
CDS Mutation c.1402C>T
AA Mutation p.Pro468Ser(p.P468S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318607
Start 100721570:100721570(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14C>T
AA Mutation p.Ala5Val(p.A5V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000318607
Start 100706732:100706732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1521C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000318607
Start 100721455:100721455(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.129C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000318607
Start 100717859:100717859(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.417C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000318607
Start 100705049:100705049(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1695G>A
Mutation Classification Silent
Feature Type Transcript