Primary Site >> Esophagus Cancer

Gene >> CENPF

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000366955
Start 214620856:214620856(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.775T>G
AA Mutation p.Leu259Val(p.L259V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366955
Start 214641406:214641406(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3068T>G
AA Mutation p.Leu1023Arg(p.L1023R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366955
Start 214651872:214651872(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8146G>A
AA Mutation p.Asp2716Asn(p.D2716N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000366955
Start 214629112:214629112(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1135G>A
AA Mutation p.Glu379Lys(p.E379K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000366955
Start 214642825:214642840(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4492_4507delGCTCTTTTAGAACAGA
AA Mutation p.Ala1498GlnfsTer7(p.A1498Qfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000366955
Start 214640898:214640898(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2560G>T
AA Mutation p.Glu854Ter(p.E854*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript