Mutation

Primary Site >> Liver Cancer

Gene >> ALB

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73420272:73420272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1804G>T
AA Mutation	p.Ala602Ser(p.A602S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73409392:73409392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520T>C
AA Mutation	p.Tyr174His(p.Y174H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73406677:73406677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763937998
CDS Mutation	c.186T>G
AA Mutation	p.Asp62Glu(p.D62E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73404377:73404377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50A>G
AA Mutation	p.Tyr17Cys(p.Y17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73418149:73418149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1490T>A
AA Mutation	p.Val497Asp(p.V497D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73412084:73412084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.802G>A
AA Mutation	p.Glu268Lys(p.E268K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73419535:73419535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1681C>T
AA Mutation	p.Pro561Ser(p.P561S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73413481:73413481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905G>T
AA Mutation	p.Cys302Phe(p.C302F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73409398:73409398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526C>G
AA Mutation	p.Pro176Ala(p.P176A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73419536:73419536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1682C>G
AA Mutation	p.Pro561Arg(p.P561R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73415096:73415096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120G>T
AA Mutation	p.Ala374Ser(p.A374S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73406741:73406741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>C
AA Mutation	p.Glu84Gln(p.E84Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73416278:73416278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214T>C
AA Mutation	p.Val405Ala(p.V405A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73405143:73405143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107A>G
AA Mutation	p.Lys36Arg(p.K36R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73418286:73418286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1627A>G
AA Mutation	p.Lys543Glu(p.K543E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73415076:73415076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1100T>C
AA Mutation	p.Val367Ala(p.V367A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73415049:73415049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537985931
CDS Mutation	c.1073A>G
AA Mutation	p.Tyr358Cys(p.Y358C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73418118:73418118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459T>G
AA Mutation	p.Leu487Val(p.L487V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000295897
Start	73409482:73409482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.610C>A
AA Mutation	p.Pro204Thr(p.P204T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295897
Start	73413554:73413554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.978G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73410363:73410379(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.669_685delGTGTGCCAGTCTCCAAA
AA Mutation	p.Cys224IlefsTer22(p.C224Ifs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73417585:73417589(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1344_1348delAGAGG
AA Mutation	p.Glu449LeufsTer13(p.E449Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73416275:73416275(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1212delT
AA Mutation	p.Val405TrpfsTer7(p.V405Wfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73419585:73419594(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1731_1740delTTTTGTAGAG
AA Mutation	p.Phe578SerfsTer27(p.F578Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73420290:73420290(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1823delG
AA Mutation	p.Gly608AlafsTer35(p.G608Afs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73406740:73406740(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.249delT
AA Mutation	p.Glu84LysfsTer57(p.E84Kfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73420292:73420295(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1824_1827delCTTA
AA Mutation	p.Leu609AsnfsTer33(p.L609Nfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73417541:73417542(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1300_1301delCG
AA Mutation	p.Arg434LeufsTer29(p.R434Lfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73417636:73417643(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1395_1402delTGAAGCAA
AA Mutation	p.Glu466LysfsTer21(p.E466Kfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73406742:73406742(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.254delA
AA Mutation	p.Asn85IlefsTer56(p.N85Ifs*56)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73419512:73419569(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1658_1715delTTGTTGAGCTCGTGAAACACAAGCCCAAGGCAACAAAAGAGCAACTGAAAGCTGTTAT
AA Mutation	p.Leu553ArgfsTer8(p.L553Rfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73408800:73408801(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.482dupA
AA Mutation	p.Tyr162IlefsTer4(p.Y162Ifs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73419578:73419579(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1725dupC
AA Mutation	p.Ala576ArgfsTer11(p.A576Rfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73408670:73408671(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.351dupA
AA Mutation	p.Gln118ThrfsTer4(p.Q118Tfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73408662:73408663(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.339_340insAGCA
AA Mutation	p.Cys114SerfsTer9(p.C114Sfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73406675:73406676(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.185_188dupATCA
AA Mutation	p.His63GlnfsTer8(p.H63Qfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295897
Start	73417580:73417581(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1341dupT
AA Mutation	p.Val448CysfsTer16(p.V448Cfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	38
Mutation Consequence	splice_donor_variant;coding_sequence_variant
Transcription ID	ENST00000295897
Start	73416341:73416354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1277_1289+1delAATTCCAGAATGCG
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	39
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant
Transcription ID	ENST00000295897
Start	73420252:73420288(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1787_1823delGTAAAAAACTTGTTGCTGCAAGTCAAGCTGCCTTAGG
AA Mutation	p.Gly596AlafsTer35(p.X596_splice)
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	40
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000295897
Start	73416355:73416355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	41
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000295897
Start	73417523:73417534(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1290-6_1295delTTTCAGGCTATT
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	42
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000295897
Start	73418115:73418117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1456_1458delGTG
AA Mutation	p.Val486del(p.V486del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	43
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000295897
Start	73413496:73413498(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.922_924delTTG
AA Mutation	p.Leu308del(p.L308del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

ID	44
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000295897
Start	73406718:73406723(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.227_232delCATGTG
AA Mutation	p.Thr76_Val78delinsIle(p.T76_V78delinsI)
Mutation Classification	In_Frame_Del
Feature Type	Transcript