Primary Site >> Esophagus Cancer

Gene >> YY1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262238
Start 100239666:100239666(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748178185
CDS Mutation c.422G>A
AA Mutation p.Gly141Asp(p.G141D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262238
Start 100239668:100239668(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.424G>A
AA Mutation p.Asp142Asn(p.D142N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262238
Start 100277485:100277485(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1130A>G
AA Mutation p.His377Arg(p.H377R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000262238
Start 100262306:100262307(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.690dupA
AA Mutation p.Asp231ArgfsTer3(p.D231Rfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 5
Mutation Consequence inframe_insertion;splice_region_variant
Transcription ID ENST00000262238
Start 100262466:100262467(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.842_842+1insAAT
AA Mutation p.Arg281_Met282insIle(p.R281_M282insI)
Mutation Classification In_Frame_Ins
Feature Type Transcript