Primary Site >> Liver Cancer

Gene >> MACC1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000332878
Start 20159693:20159693(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.668G>T
AA Mutation p.Gly223Val(p.G223V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000332878
Start 20158919:20158919(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1442A>G
AA Mutation p.His481Arg(p.H481R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000332878
Start 20154291:20154291(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2248T>A
AA Mutation p.Trp750Arg(p.W750R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000332878
Start 20159376:20159376(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.985T>A
AA Mutation p.Tyr329Asn(p.Y329N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000332878
Start 20160231:20160231(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.130G>T
AA Mutation p.Asp44Tyr(p.D44Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000332878
Start 20161748:20161748(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.115G>A
AA Mutation p.Glu39Lys(p.E39K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000332878
Start 20159787:20159787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.574T>A
AA Mutation p.Cys192Ser(p.C192S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000332878
Start 20159938:20159938(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.423A>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000332878
Start 20159317:20159317(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1044T>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000332878
Start 20158588:20158588(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1773G>A
Mutation Classification Silent
Feature Type Transcript