Primary Site >> Stomach Cancer

Gene >> NDRG1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000323851
Start 133264634:133264634(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.118T>G
AA Mutation p.Leu40Val(p.L40V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000323851
Start 133248741:133248741(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.729G>A
AA Mutation p.Met243Ile(p.M243I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000323851
Start 133262051:133262051(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144310406
CDS Mutation c.322G>A
AA Mutation p.Ala108Thr(p.A108T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000323851
Start 133254562:133254562(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.571G>T
AA Mutation p.Val191Leu(p.V191L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000323851
Start 133244375:133244375(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774885520
CDS Mutation c.871G>A
AA Mutation p.Gly291Ser(p.G291S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000323851
Start 133256816:133256816(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.498C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000323851
Start 133264557:133264557(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.195C>A
Mutation Classification Silent
Feature Type Transcript