Primary Site >> Stomach Cancer

Gene >> NR2E1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368986
Start 108171461:108171461(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.29G>A
AA Mutation p.Arg10His(p.R10H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368986
Start 108178209:108178209(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.610C>T
AA Mutation p.Pro204Ser(p.P204S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000368986
Start 108187373:108187373(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1068A>G
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000368986
Start 108187395:108187395(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1096delA
AA Mutation p.Thr366ProfsTer46(p.T366Pfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000368986
Start 108187394:108187395(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1096dupA
AA Mutation p.Thr366AsnfsTer19(p.T366Nfs*19)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript