Primary Site >> Stomach Cancer

Gene >> LCOR

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356016
Start 96955165:96955165(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.545A>T
AA Mutation p.Asn182Ile(p.N182I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356016
Start 96955837:96955837(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763089848
CDS Mutation c.1217C>T
AA Mutation p.Ser406Leu(p.S406L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356016
Start 96955531:96955531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.911T>C
AA Mutation p.Met304Thr(p.M304T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000356016
Start 96955268:96955268(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.648C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000356016
Start 96955172:96955172(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.552A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000356016
Start 96955313:96955313(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.697delA
AA Mutation p.Met233TrpfsTer13(p.M233Wfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript