Primary Site >> Stomach Cancer

Gene >> MAP7D2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000379651
Start 20010837:20010837(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2165C>T
AA Mutation p.Pro722Leu(p.P722L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence stop_gained
Transcription ID ENST00000379651
Start 20064752:20064752(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.184C>T
AA Mutation p.Arg62Ter(p.R62*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence stop_gained
Transcription ID ENST00000379651
Start 20063506:20063506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.280C>T
AA Mutation p.Arg94Ter(p.R94*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence stop_gained
Transcription ID ENST00000379651
Start 20024976:20024976(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1264C>T
AA Mutation p.Arg422Ter(p.R422*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript