Primary Site >> Liver Cancer

Gene >> LAMC2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264144
Start 183215494:183215494(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.310T>A
AA Mutation p.Cys104Ser(p.C104S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264144
Start 183240377:183240377(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3314T>A
AA Mutation p.Leu1105His(p.L1105H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264144
Start 183220910:183220910(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.589C>A
AA Mutation p.Arg197Ser(p.R197S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264144
Start 183238328:183238328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2776C>A
AA Mutation p.Arg926Ser(p.R926S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264144
Start 183239411:183239411(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2917A>T
AA Mutation p.Met973Leu(p.M973L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264144
Start 183240094:183240094(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3124A>T
AA Mutation p.Met1042Leu(p.M1042L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264144
Start 183235698:183235698(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2424G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264144
Start 183232839:183232839(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2202A>G
Mutation Classification Silent
Feature Type Transcript