Primary Site >> Liver Cancer

Gene >> LRRC4C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40114894:40114894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1399G>A
AA Mutation p.Asp467Asn(p.D467N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40115880:40115880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.413C>A
AA Mutation p.Thr138Asn(p.T138N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40115877:40115877(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.416T>C
AA Mutation p.Ile139Thr(p.I139T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40115772:40115772(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.521T>C
AA Mutation p.Leu174Ser(p.L174S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40115629:40115629(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.664G>T
AA Mutation p.Asp222Tyr(p.D222Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000278198
Start 40114657:40114657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1636A>G
AA Mutation p.Ile546Val(p.I546V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000278198
Start 40116101:40116101(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.192G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000278198
Start 40116103:40116103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.190C>A
Mutation Classification Silent
Feature Type Transcript