Primary Site >> Liver Cancer

Gene >> EPHA8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000166244
Start 22601635:22601635(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139543017
CDS Mutation c.2912G>A
AA Mutation p.Arg971His(p.R971H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000166244
Start 22576337:22576337(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758018689
CDS Mutation c.280G>A
AA Mutation p.Ala94Thr(p.A94T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000166244
Start 22589192:22589192(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1301C>T
AA Mutation p.Thr434Ile(p.T434I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000166244
Start 22576333:22576333(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145476843
CDS Mutation c.276C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000166244
Start 22576468:22576468(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.411A>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000166244
Start 22596124:22596124(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1716G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000166244
Start 22569288:22569288(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.95-1G>A
Mutation Classification Splice_Site
Feature Type Transcript