Primary Site >> Liver Cancer

Gene >> BOC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355385
Start 113278774:113278774(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770329941
CDS Mutation c.1804C>T
AA Mutation p.Arg602Cys(p.R602C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355385
Start 113272635:113272635(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771932279
CDS Mutation c.893G>A
AA Mutation p.Arg298His(p.R298H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355385
Start 113286795:113286795(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3278C>A
AA Mutation p.Pro1093His(p.P1093H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000355385
Start 113250564:113250564(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.107C>T
AA Mutation p.Pro36Leu(p.P36L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000355385
Start 113278182:113278182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1627A>T
AA Mutation p.Ser543Cys(p.S543C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000355385
Start 113285516:113285516(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3108C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000355385
Start 113268441:113268441(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.519C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000355385
Start 113274529:113274529(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1389A>T
Mutation Classification Silent
Feature Type Transcript