Primary Site >> Liver Cancer

Gene >> LAMB2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305544
Start 49129118:49129118(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1633C>G
AA Mutation p.Gln545Glu(p.Q545E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305544
Start 49124056:49124056(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747064604
CDS Mutation c.3469C>T
AA Mutation p.Arg1157Cys(p.R1157C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000305544
Start 49125087:49125087(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2803A>G
AA Mutation p.Ser935Gly(p.S935G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000305544
Start 49128729:49128729(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1822C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000305544
Start 49123627:49123627(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3802G>T
AA Mutation p.Glu1268Ter(p.E1268*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000305544
Start 49125485:49125485(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2489-1G>T
Mutation Classification Splice_Site
Feature Type Transcript
ID 7
Mutation Consequence inframe_deletion
Transcription ID ENST00000305544
Start 49125358:49125381(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2592_2615delCCAGCGTGGCCAGTGGGGATTCCC
AA Mutation p.Gln865_Pro872del(p.Q865_P872del)
Mutation Classification In_Frame_Del
Feature Type Transcript