Primary Site >> Liver Cancer

Gene >> THEMIS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127813905:127813905(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.736C>A
AA Mutation p.Pro246Thr(p.P246T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127813013:127813013(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768563536
CDS Mutation c.1628T>C
AA Mutation p.Met543Thr(p.M543T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127813709:127813709(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.932A>G
AA Mutation p.Lys311Arg(p.K311R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127812974:127812974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1667G>A
AA Mutation p.Arg556His(p.R556H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000368248
Start 127813747:127813747(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.894A>T
AA Mutation p.Gln298His(p.Q298H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000368248
Start 127813906:127813906(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.735C>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000368248
Start 127829720:127829720(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.465A>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000368248
Start 127813929:127813929(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.712C>T
AA Mutation p.Arg238Ter(p.R238*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript