Primary Site >> Esophagus Cancer

Gene >> FBXW7

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000281708
Start 152326043:152326043(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1607C>G
AA Mutation p.Thr536Arg(p.T536R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000281708
Start 152326137:152326137(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1513C>G
AA Mutation p.Arg505Gly(p.R505G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000281708
Start 152326137:152326137(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149680468
CDS Mutation c.1513C>T
AA Mutation p.Arg505Cys(p.R505C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000281708
Start 152324312:152324312(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1727C>T
AA Mutation p.Thr576Met(p.T576M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000281708
Start 152323004:152323004(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2001delG
AA Mutation p.Ser668ValfsTer39(p.S668Vfs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000281708
Start 152323086:152323086(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1919delG
AA Mutation p.Ser640ThrfsTer7(p.S640Tfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000281708
Start 152411319:152411335(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.469_485delCTCTCCTCCCCATTCTA
AA Mutation p.Leu157TyrfsTer15(p.L157Yfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000281708
Start 152329731:152329731(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1177C>T
AA Mutation p.Arg393Ter(p.R393*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000281708
Start 152411587:152411587(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.217C>T
AA Mutation p.Gln73Ter(p.Q73*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000281708
Start 152328208:152328209(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1417dupA
AA Mutation p.Arg473LysfsTer4(p.R473Kfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript