Primary Site >> Liver Cancer

Gene >> SLC8A1

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000332839
Start 40160765:40160765(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2269G>T
AA Mutation p.Gly757Trp(p.G757W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332839
Start 40429243:40429243(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760339904
CDS Mutation c.1038A>G
AA Mutation p.Ile346Met(p.I346M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332839
Start 40429463:40429463(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.818G>T
AA Mutation p.Gly273Val(p.G273V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000332839
Start 40429837:40429837(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.444G>T
AA Mutation p.Glu148Asp(p.E148D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000332839
Start 40428897:40428897(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1384G>A
AA Mutation p.Gly462Arg(p.G462R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000332839
Start 40428843:40428843(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1438A>T
AA Mutation p.Ile480Leu(p.I480L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000332839
Start 40428561:40428561(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1720T>C
AA Mutation p.Tyr574His(p.Y574H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000332839
Start 40429696:40429696(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.585A>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000332839
Start 40428931:40428931(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1350A>T
Mutation Classification Silent
Feature Type Transcript