Primary Site >> Liver Cancer

Gene >> CCDC88C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000389857
Start 91313412:91313412(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2404G>C
AA Mutation p.Asp802His(p.D802H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000389857
Start 91313481:91313481(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2335A>C
AA Mutation p.Ser779Arg(p.S779R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000389857
Start 91321178:91321178(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778090862
CDS Mutation c.1469A>T
AA Mutation p.Glu490Val(p.E490V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000389857
Start 91303904:91303904(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3432G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000389857
Start 91303886:91303886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3450C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000389857
Start 91313839:91313839(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1977G>A
Mutation Classification Silent
Feature Type Transcript