Primary Site >> Liver Cancer

Gene >> CCDC180

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000529487
Start 97343524:97343524(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2591T>C
AA Mutation p.Val864Ala(p.V864A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000529487
Start 97343392:97343392(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2459C>G
AA Mutation p.Ser820Cys(p.S820C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000529487
Start 97318578:97318578(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1207A>T
AA Mutation p.Ile403Phe(p.I403F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000529487
Start 97355006:97355006(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3394C>G
AA Mutation p.Gln1132Glu(p.Q1132E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000529487
Start 97343471:97343471(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2538C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000529487
Start 97354650:97354650(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3216A>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000529487
Start 97362319:97362319(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3912A>T
Mutation Classification Silent
Feature Type Transcript