Primary Site >> Stomach Cancer

Gene >> AGXT

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307503
Start 240878085:240878085(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767927978
CDS Mutation c.1006G>A
AA Mutation p.Val336Ile(p.V336I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000307503
Start 240878091:240878091(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1012T>G
AA Mutation p.Tyr338Asp(p.Y338D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000307503
Start 240878752:240878752(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375318394
CDS Mutation c.1110C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000307503
Start 240868940:240868940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.75G>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000307503
Start 240868891:240868891(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs768991178
CDS Mutation c.33delC
AA Mutation p.Lys12ArgfsTer34(p.K12Rfs*34)
Mutation Classification Frame_Shift_Del
Feature Type Transcript