Primary Site >> Liver Cancer

Gene >> GOLGA4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37361264:37361264(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6685A>G
AA Mutation p.Ile2229Val(p.I2229V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37325317:37325317(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758806004
CDS Mutation c.3431A>G
AA Mutation p.Asn1144Ser(p.N1144S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37325947:37325947(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4061C>A
AA Mutation p.Ala1354Asp(p.A1354D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37329067:37329067(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6166G>T
AA Mutation p.Ala2056Ser(p.A2056S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37286022:37286022(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.486A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37298952:37298952(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.934T>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000361924
Start 37355100:37355100(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6577-1G>A
Mutation Classification Splice_Site
Feature Type Transcript