Mutation

Primary Site >> Liver Cancer

Gene >> PCLO

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82822685:82822685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14601G>T
AA Mutation	p.Met4867Ile(p.M4867I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82954778:82954778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6175C>G
AA Mutation	p.Leu2059Val(p.L2059V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82835676:82835676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14240A>G
AA Mutation	p.Gln4747Arg(p.Q4747R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82953532:82953532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7421C>A
AA Mutation	p.Pro2474His(p.P2474H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83135005:83135005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547726879
CDS Mutation	c.2545G>A
AA Mutation	p.Val849Ile(p.V849I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82915403:82915403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12583C>A
AA Mutation	p.Leu4195Ile(p.L4195I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82956491:82956491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4462C>T
AA Mutation	p.Pro1488Ser(p.P1488S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82956551:82956551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4402A>G
AA Mutation	p.Ile1468Val(p.I1468V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82955039:82955039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5914A>G
AA Mutation	p.Ser1972Gly(p.S1972G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82953305:82953305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7648G>T
AA Mutation	p.Ala2550Ser(p.A2550S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82966209:82966209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765390976
CDS Mutation	c.3579A>T
AA Mutation	p.Gln1193His(p.Q1193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83135013:83135013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2537T>A
AA Mutation	p.Val846Asp(p.V846D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82916686:82916686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11300A>T
AA Mutation	p.Asp3767Val(p.D3767V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82966378:82966378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3410T>A
AA Mutation	p.Met1137Lys(p.M1137K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82916622:82916622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11364T>A
AA Mutation	p.Asp3788Glu(p.D3788E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82916705:82916705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11281A>C
AA Mutation	p.Lys3761Gln(p.K3761Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82954184:82954184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6769G>T
AA Mutation	p.Ala2257Ser(p.A2257S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83135564:83135564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1986G>T
AA Mutation	p.Lys662Asn(p.K662N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82954193:82954193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6760G>A
AA Mutation	p.Asp2254Asn(p.D2254N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82902657:82902657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13522G>A
AA Mutation	p.Val4508Ile(p.V4508I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82838333:82838333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767862283
CDS Mutation	c.14107A>G
AA Mutation	p.Asn4703Asp(p.N4703D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82951969:82951969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8984C>A
AA Mutation	p.Ser2995Tyr(p.S2995Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83135409:83135409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2141G>T
AA Mutation	p.Gly714Val(p.G714V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82914755:82914755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13231A>G
AA Mutation	p.Thr4411Ala(p.T4411A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82956074:82956074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4879C>T
AA Mutation	p.His1627Tyr(p.H1627Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82952225:82952225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547500251
CDS Mutation	c.8728G>A
AA Mutation	p.Val2910Ile(p.V2910I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83155530:83155530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1111C>A
AA Mutation	p.Pro371Thr(p.P371T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82805752:82805752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14869A>G
AA Mutation	p.Ser4957Gly(p.S4957G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83155151:83155151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1490C>T
AA Mutation	p.Ala497Val(p.A497V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83155440:83155440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1201C>A
AA Mutation	p.Pro401Thr(p.P401T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82915522:82915522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199931189
CDS Mutation	c.12464A>G
AA Mutation	p.Tyr4155Cys(p.Y4155C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82879342:82879342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556966262
CDS Mutation	c.13649T>C
AA Mutation	p.Met4550Thr(p.M4550T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82953435:82953435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7518C>A
AA Mutation	p.Ser2506Arg(p.S2506R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82915993:82915993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11993C>T
AA Mutation	p.Ala3998Val(p.A3998V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82950744:82950744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9844A>T
AA Mutation	p.Arg3282Trp(p.R3282W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82952707:82952707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8246C>A
AA Mutation	p.Ala2749Asp(p.A2749D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82822682:82822682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14604G>T
AA Mutation	p.Gln4868His(p.Q4868H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83134878:83134878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2672C>A
AA Mutation	p.Thr891Lys(p.T891K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82954145:82954145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780885885
CDS Mutation	c.6808G>A
AA Mutation	p.Ala2270Thr(p.A2270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	83135154:83135154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2396C>G
AA Mutation	p.Ser799Cys(p.S799C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82955030:82955030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5923A>G
AA Mutation	p.Thr1975Ala(p.T1975A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82955032:82955032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5921T>C
AA Mutation	p.Leu1974Pro(p.L1974P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82805823:82805823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14798C>T
AA Mutation	p.Pro4933Leu(p.P4933L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000333891
Start	82956269:82956269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4684G>A
AA Mutation	p.Glu1562Lys(p.E1562K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	83162554:83162554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.39C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82953924:82953924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7029A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82950880:82950880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9708G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82760645:82760645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15282T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82966146:82966146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3642C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82953950:82953950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7003T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82966080:82966080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3708A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82953393:82953393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7560A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82951393:82951393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9195A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82951201:82951201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776093952
CDS Mutation	c.9387A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	82916586:82916586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764033539
CDS Mutation	c.11400C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	56
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	83162485:83162485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	57
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333891
Start	83155978:83155978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.663G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	58
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333891
Start	82953311:82953320(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.7633_7642delAATTTAGTGA
AA Mutation	p.Asn2545LeufsTer34(p.N2545Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	59
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333891
Start	82955834:82955841(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5112_5119delGACAGACT
AA Mutation	p.Asp1706Ter(p.D1706*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	60
Mutation Consequence	stop_gained
Transcription ID	ENST00000333891
Start	82908996:82908996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13318G>T
AA Mutation	p.Glu4440Ter(p.E4440*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	61
Mutation Consequence	stop_gained
Transcription ID	ENST00000333891
Start	82954784:82954784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6169A>T
AA Mutation	p.Lys2057Ter(p.K2057*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	62
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333891
Start	82760738:82760739(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.15188dupA
AA Mutation	p.Val5064GlyfsTer12(p.V5064Gfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript