Primary Site >> Liver Cancer

Gene >> TPO

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1516955:1516955(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2591G>T
AA Mutation p.Gly864Val(p.G864V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1433592:1433592(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.334T>C
AA Mutation p.Ser112Pro(p.S112P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1484603:1484603(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1346C>T
AA Mutation p.Thr449Ile(p.T449I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1496038:1496038(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2056C>A
AA Mutation p.Leu686Met(p.L686M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1456096:1456096(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.633T>A
AA Mutation p.His211Gln(p.H211Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1456097:1456097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.634G>T
AA Mutation p.Val212Phe(p.V212F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1496032:1496032(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771942015
CDS Mutation c.2050C>T
AA Mutation p.Arg684Cys(p.R684C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1477242:1477242(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.976G>T
AA Mutation p.Ala326Ser(p.A326S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1433532:1433532(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.274G>A
AA Mutation p.Glu92Lys(p.E92K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1484791:1484791(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1534C>T
AA Mutation p.Pro512Ser(p.P512S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1493835:1493835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1802C>A
AA Mutation p.Pro601His(p.P601H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000329066
Start 1436384:1436384(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.482G>T
AA Mutation p.Arg161Ile(p.R161I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1477183:1477183(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.917G>C
AA Mutation p.Gly306Ala(p.G306A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000329066
Start 1477241:1477241(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.975C>A
AA Mutation p.Asp325Glu(p.D325E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000329066
Start 1477268:1477268(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1002G>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000329066
Start 1436367:1436367(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.465A>T
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000329066
Start 1477334:1477334(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1068C>T
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000329066
Start 1456162:1456162(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.699G>A
AA Mutation p.Trp233Ter(p.W233*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript