Primary Site >> Stomach Cancer

Gene >> PGAP3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000300658
Start 39674042:39674042(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.508T>C
AA Mutation p.Phe170Leu(p.F170L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000300658
Start 39685973:39685973(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.228C>A
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000300658
Start 39673122:39673122(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375997053
CDS Mutation c.828G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000300658
Start 39673998:39673998(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147768703
CDS Mutation c.552C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000300658
Start 39673551:39673551(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372234504
CDS Mutation c.657C>T
Mutation Classification Silent
Feature Type Transcript