Primary Site >> Esophagus Cancer

Gene >> CCDC80

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000206423
Start 112639646:112639646(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.260G>A
AA Mutation p.Arg87His(p.R87H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000206423
Start 112618994:112618994(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2146C>A
AA Mutation p.Leu716Ile(p.L716I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000206423
Start 112638995:112638995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.911C>T
AA Mutation p.Pro304Leu(p.P304L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000206423
Start 112639729:112639729(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.177C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000206423
Start 112605585:112605585(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2685G>A
Mutation Classification Silent
Feature Type Transcript