Primary Site >> Stomach Cancer

Gene >> GLDC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321612
Start 6595052:6595052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1223C>A
AA Mutation p.Ala408Asp(p.A408D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321612
Start 6595109:6595109(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121964979
CDS Mutation c.1166C>T
AA Mutation p.Ala389Val(p.A389V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321612
Start 6550862:6550862(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2510C>T
AA Mutation p.Ala837Val(p.A837V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321612
Start 6610292:6610292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.535T>C
AA Mutation p.Tyr179His(p.Y179H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321612
Start 6604759:6604759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs386833591
CDS Mutation c.887T>G
AA Mutation p.Leu296Arg(p.L296R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000321612
Start 6610288:6610288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.539A>G
AA Mutation p.Gln180Arg(p.Q180R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000321612
Start 6610217:6610217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.610G>T
AA Mutation p.Ala204Ser(p.A204S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000321612
Start 6605272:6605272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.720T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000321612
Start 6553433:6553433(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2392G>T
AA Mutation p.Gly798Ter(p.G798*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript