Primary Site >> Liver Cancer

Gene >> EPHB2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000400191
Start 22864934:22864934(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1025T>A
AA Mutation p.Leu342Gln(p.L342Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000400191
Start 22909095:22909095(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759393577
CDS Mutation c.2426T>C
AA Mutation p.Val809Ala(p.V809A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000400191
Start 22906865:22906865(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779022970
CDS Mutation c.2044G>A
AA Mutation p.Val682Ile(p.V682I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000400191
Start 22905996:22905996(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1775G>T
AA Mutation p.Gly592Val(p.G592V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000400191
Start 22906012:22906012(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745346872
CDS Mutation c.1791C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000400191
Start 22895551:22895551(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1671T>A
Mutation Classification Silent
Feature Type Transcript