Primary Site >> Liver Cancer

Gene >> TRO

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000173898
Start 54928660:54928660(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1936G>A
AA Mutation p.Glu646Lys(p.E646K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000173898
Start 54929407:54929407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2683A>T
AA Mutation p.Thr895Ser(p.T895S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000173898
Start 54929123:54929123(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2399G>T
AA Mutation p.Ser800Ile(p.S800I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000173898
Start 54923364:54923364(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.832C>A
AA Mutation p.Leu278Ile(p.L278I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000173898
Start 54930207:54930207(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3483T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000173898
Start 54930939:54930939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4215C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000173898
Start 54930618:54930618(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3894T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000173898
Start 54929135:54929165(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2411_2441delGTTTCAGCAGTGAAGCCAGCATTAGCTTTGG
AA Mutation p.Ser804MetfsTer140(p.S804Mfs*140)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000173898
Start 54923025:54923025(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.493C>T
AA Mutation p.Gln165Ter(p.Q165*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript