Primary Site >> Liver Cancer

Gene >> CHRNA4

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370263
Start 63346773:63346773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1849C>T
AA Mutation p.Leu617Phe(p.L617F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370263
Start 63346776:63346776(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1846G>T
AA Mutation p.Gly616Cys(p.G616C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370263
Start 63349706:63349706(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1705G>A
AA Mutation p.Glu569Lys(p.E569K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370263
Start 63359609:63359609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.167C>T
AA Mutation p.Ala56Val(p.A56V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370263
Start 63349765:63349765(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1646G>C
AA Mutation p.Arg549Pro(p.R549P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000370263
Start 63350595:63350595(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.816C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000370263
Start 63349701:63349701(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript