Primary Site >> Liver Cancer

Gene >> TRIM67

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000366653
Start 231209145:231209145(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2018C>T
AA Mutation p.Ala673Val(p.A673V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000366653
Start 231201379:231201379(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370312974
CDS Mutation c.1396C>T
AA Mutation p.Arg466Cys(p.R466C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000366653
Start 231163643:231163643(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.674A>T
AA Mutation p.Gln225Leu(p.Q225L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000366653
Start 231163965:231163965(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000366653
Start 231213845:231213845(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200465476
CDS Mutation c.2154C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000366653
Start 231213962:231213962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2271C>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000366653
Start 231209110:231209111(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1985dupA
AA Mutation p.Asn662LysfsTer24(p.N662Kfs*24)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript