Primary Site >> Liver Cancer

Gene >> TLR8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000218032
Start 12921402:12921402(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2362G>A
AA Mutation p.Asp788Asn(p.D788N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000218032
Start 12919623:12919623(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.583G>A
AA Mutation p.Gly195Arg(p.G195R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000218032
Start 12921604:12921604(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2564A>T
AA Mutation p.Asp855Val(p.D855V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000218032
Start 12919270:12919270(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745722261
CDS Mutation c.230A>G
AA Mutation p.His77Arg(p.H77R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000218032
Start 12919309:12919309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.269C>G
AA Mutation p.Thr90Ser(p.T90S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000218032
Start 12921064:12921064(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2024T>C
AA Mutation p.Met675Thr(p.M675T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000218032
Start 12921898:12921898(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2858G>C
AA Mutation p.Ser953Thr(p.S953T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000218032
Start 12920294:12920294(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1254C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000218032
Start 12920633:12920633(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1593T>C
Mutation Classification Silent
Feature Type Transcript