Primary Site >> Liver Cancer

Gene >> TRIP12

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000283943
Start 229859126:229859126(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.547G>A
AA Mutation p.Ala183Thr(p.A183T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000283943
Start 229774182:229774182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5384C>G
AA Mutation p.Thr1795Ser(p.T1795S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000283943
Start 229807746:229807746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2314T>A
AA Mutation p.Trp772Arg(p.W772R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000283943
Start 229803579:229803579(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2765G>A
AA Mutation p.Arg922Lys(p.R922K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000283943
Start 229799001:229799001(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3131G>T
AA Mutation p.Ser1044Ile(p.S1044I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000283943
Start 229859380:229859380(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs532583604
CDS Mutation c.293C>T
AA Mutation p.Thr98Ile(p.T98I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000283943
Start 229859233:229859233(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.440A>T
AA Mutation p.Gln147Leu(p.Q147L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000283943
Start 229787529:229787529(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4746T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000283943
Start 229767722:229767722(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750607517
CDS Mutation c.5811A>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000283943
Start 229791131:229791131(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4311A>G
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000283943
Start 229792027:229792027(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4029G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000283943
Start 229802338:229802338(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2895C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000283943
Start 229774136:229774136(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5430T>C
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000283943
Start 229796611:229796611(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3571delC
AA Mutation p.His1191MetfsTer28(p.H1191Mfs*28)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000283943
Start 229792991:229792991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3898A>T
AA Mutation p.Arg1300Ter(p.R1300*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript