Primary Site >> Liver Cancer

Gene >> PER1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000317276
Start 8150062:8150062(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.438G>C
AA Mutation p.Lys146Asn(p.K146N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000317276
Start 8148662:8148662(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769554705
CDS Mutation c.1030A>G
AA Mutation p.Ile344Val(p.I344V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000317276
Start 8146434:8146434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1976C>T
AA Mutation p.Thr659Ile(p.T659I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000317276
Start 8146676:8146676(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1825G>T
AA Mutation p.Ala609Ser(p.A609S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000317276
Start 8143340:8143376(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2962_2998delCAGCTGGAGGAGCTCCCCCGTGCTGAGGGGGCTGCTG
AA Mutation p.Gln988LeufsTer122(p.Q988Lfs*122)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000317276
Start 8145981:8145981(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2195delG
AA Mutation p.Gly732GlufsTer12(p.G732Efs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript