Primary Site >> Stomach Cancer

Gene >> GC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000273951
Start 71755021:71755021(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1121A>G
AA Mutation p.Glu374Gly(p.E374G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000273951
Start 71756806:71756806(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.940T>G
AA Mutation p.Phe314Val(p.F314V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000273951
Start 71752580:71752580(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs3737553
CDS Mutation c.1333C>T
AA Mutation p.His445Tyr(p.H445Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000273951
Start 71768308:71768308(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.254A>G
AA Mutation p.Asp85Gly(p.D85G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000273951
Start 71765558:71765558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.347G>A
AA Mutation p.Gly116Asp(p.G116D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000273951
Start 71765471:71765471(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.434G>A
AA Mutation p.Cys145Tyr(p.C145Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000273951
Start 71768334:71768334(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.228G>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000273951
Start 71752551:71752551(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1362C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000273951
Start 71758147:71758147(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.726delA
AA Mutation p.Val243CysfsTer12(p.V243Cfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000273951
Start 71758078:71758078(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.795C>A
AA Mutation p.Cys265Ter(p.C265*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript