Primary Site >> Stomach Cancer

Gene >> SP6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000342234
Start 47848309:47848309(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780881543
CDS Mutation c.121G>A
AA Mutation p.Gly41Arg(p.G41R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000342234
Start 47847365:47847365(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1065C>T
Mutation Classification Silent
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000342234
Start 47848100:47848100(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769192100
CDS Mutation c.330G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000342234
Start 47847623:47847623(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.807G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000342234
Start 47848088:47848088(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.342C>T
Mutation Classification Silent
Feature Type Transcript