Primary Site >> Stomach Cancer

Gene >> C2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000299367
Start 31945275:31945275(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147553278
CDS Mutation c.2177G>A
AA Mutation p.Arg726Gln(p.R726Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000299367
Start 31945277:31945277(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2179G>A
AA Mutation p.Asp727Asn(p.D727N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000299367
Start 31933895:31933895(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.645C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000299367
Start 31933704:31933704(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776980619
CDS Mutation c.537G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000299367
Start 31934236:31934236(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.786G>A
Mutation Classification Silent
Feature Type Transcript