Primary Site >> Liver Cancer

Gene >> CACNA1H

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000348261
Start 1210417:1210417(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3893A>G
AA Mutation p.His1298Arg(p.H1298R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000348261
Start 1220071:1220071(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6139A>G
AA Mutation p.Arg2047Gly(p.R2047G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000348261
Start 1204427:1204427(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773952204
CDS Mutation c.2420C>T
AA Mutation p.Thr807Met(p.T807M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000348261
Start 1219083:1219083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763114755
CDS Mutation c.6001C>T
AA Mutation p.Arg2001Trp(p.R2001W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000348261
Start 1200720:1200720(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1124T>A
AA Mutation p.Ile375Asn(p.I375N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000348261
Start 1213800:1213800(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4798T>C
AA Mutation p.Tyr1600His(p.Y1600H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000348261
Start 1211288:1211288(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4344T>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000348261
Start 1201935:1201935(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1485G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000348261
Start 1212101:1212101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4722G>A
Mutation Classification Silent
Feature Type Transcript