Primary Site >> Liver Cancer

Gene >> TEK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000380036
Start 27190550:27190550(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1349C>G
AA Mutation p.Ala450Gly(p.A450G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000380036
Start 27157966:27157966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.188C>A
AA Mutation p.Ala63Asp(p.A63D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000380036
Start 27158098:27158098(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.320G>T
AA Mutation p.Arg107Leu(p.R107L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000380036
Start 27203081:27203081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2171C>A
AA Mutation p.Ala724Asp(p.A724D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000380036
Start 27206597:27206597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2380G>C
AA Mutation p.Val794Leu(p.V794L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000380036
Start 27212820:27212820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2800T>C
AA Mutation p.Ser934Pro(p.S934P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000380036
Start 27228232:27228232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3227G>T
AA Mutation p.Arg1076Leu(p.R1076L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000380036
Start 27173271:27173271(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.810A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000380036
Start 27157871:27157871(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.93C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000380036
Start 27206623:27206623(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2406C>A
Mutation Classification Silent
Feature Type Transcript