Primary Site >> Liver Cancer

Gene >> ARID1B

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000350026
Start 157201237:157201237(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4604A>G
AA Mutation p.Asn1535Ser(p.N1535S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000350026
Start 157200991:157200991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4358C>A
AA Mutation p.Ala1453Glu(p.A1453E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000350026
Start 157207490:157207490(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6310A>T
AA Mutation p.Arg2104Trp(p.R2104W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000350026
Start 157200921:157200921(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4288A>G
AA Mutation p.Ile1430Val(p.I1430V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000350026
Start 157184367:157184367(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3443A>T
AA Mutation p.Glu1148Val(p.E1148V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000350026
Start 157206225:157206225(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5045T>G
AA Mutation p.Phe1682Cys(p.F1682C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000350026
Start 156829336:156829336(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1652G>A
AA Mutation p.Gly551Asp(p.G551D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000350026
Start 157181148:157181148(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3276C>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000350026
Start 157207690:157207690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6510G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000350026
Start 157084671:157084671(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2009delG
AA Mutation p.Gly670AlafsTer14(p.G670Afs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000350026
Start 156901481:156901481(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1843C>T
AA Mutation p.Gln615Ter(p.Q615*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript