Primary Site >> Esophagus Cancer

Gene >> APC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112841134:112841134(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371686531
CDS Mutation c.5540C>T
AA Mutation p.Thr1847Met(p.T1847M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112838307:112838307(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2713A>C
AA Mutation p.Ser905Arg(p.S905R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000257430
Start 112838571:112838571(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2977A>C
AA Mutation p.Lys993Gln(p.K993Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000257430
Start 112819025:112819025(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148343173
CDS Mutation c.993G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000257430
Start 112819244:112819244(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1212C>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000257430
Start 112839976:112839977(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4384_4385delAA
AA Mutation p.Lys1462GlufsTer6(p.K1462Efs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000257430
Start 112835045:112835045(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1839delT
AA Mutation p.Ala614HisfsTer16(p.A614Hfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000257430
Start 112840254:112840255(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.4666dupA
AA Mutation p.Thr1556AsnfsTer3(p.T1556Nfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000257430
Start 112815531:112815532(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.875dupT
AA Mutation p.Leu292PhefsTer4(p.L292Ffs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript