Primary Site >> Liver Cancer

Gene >> LAMA3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23838871:23838871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3184A>G
AA Mutation p.Asn1062Asp(p.N1062D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23861730:23861730(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4507G>A
AA Mutation p.Val1503Met(p.V1503M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23857971:23857971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4264G>C
AA Mutation p.Gly1422Arg(p.G1422R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23894910:23894910(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5465G>A
AA Mutation p.Cys1822Tyr(p.C1822Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23884780:23884780(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5230A>G
AA Mutation p.Thr1744Ala(p.T1744A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23943888:23943888(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9127C>A
AA Mutation p.Arg3043Ser(p.R3043S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23861739:23861739(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4516C>A
AA Mutation p.Leu1506Ile(p.L1506I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23842399:23842399(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3341A>T
AA Mutation p.Gln1114Leu(p.Q1114L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000313654
Start 23842696:23842696(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3549A>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000313654
Start 23763487:23763487(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1146C>T
Mutation Classification Silent
Feature Type Transcript