Primary Site >> Stomach Cancer

Gene >> NDRG2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000298687
Start 21020794:21020794(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768988182
CDS Mutation c.458C>T
AA Mutation p.Ala153Val(p.A153V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000298687
Start 21017993:21017993(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.943G>A
AA Mutation p.Gly315Ser(p.G315S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000298687
Start 21019950:21019950(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.582G>A
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000298687
Start 21021867:21021867(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.357A>G
Mutation Classification Silent
Feature Type Transcript