Primary Site >> Stomach Cancer

Gene >> SRC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000358208
Start 37402838:37402838(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1360C>G
AA Mutation p.Leu454Val(p.L454V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000358208
Start 37403306:37403306(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1538A>G
AA Mutation p.Glu513Gly(p.E513G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000358208
Start 37402828:37402828(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1350C>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000358208
Start 37393967:37393967(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.423G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000358208
Start 37393941:37393941(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.398delG
AA Mutation p.Gly133AlafsTer70(p.G133Afs*70)
Mutation Classification Frame_Shift_Del
Feature Type Transcript