Primary Site >> Liver Cancer

Gene >> THBS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000260356
Start 39593170:39593170(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781417873
CDS Mutation c.2938C>T
AA Mutation p.Arg980Cys(p.R980C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000260356
Start 39582729:39582729(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.604G>T
AA Mutation p.Gly202Trp(p.G202W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000260356
Start 39582735:39582735(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760002107
CDS Mutation c.610G>A
AA Mutation p.Val204Ile(p.V204I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000260356
Start 39594380:39594380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3445G>A
AA Mutation p.Gly1149Arg(p.G1149R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000260356
Start 39593667:39593667(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3266A>T
AA Mutation p.Gln1089Leu(p.Q1089L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000260356
Start 39582734:39582734(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.609C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000260356
Start 39589318:39589318(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1890C>T
Mutation Classification Silent
Feature Type Transcript