Mutation

Primary Site >> Liver Cancer

Gene >> LRP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57195280:57195280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8318C>T
AA Mutation	p.Thr2773Met(p.T2773M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57183790:57183790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5810A>G
AA Mutation	p.Tyr1937Cys(p.Y1937C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57208200:57208200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12022G>A
AA Mutation	p.Val4008Met(p.V4008M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57211211:57211211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12952T>C
AA Mutation	p.Cys4318Arg(p.C4318R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57180084:57180084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5179G>A
AA Mutation	p.Ala1727Thr(p.A1727T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57209862:57209862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12433C>T
AA Mutation	p.Pro4145Ser(p.P4145S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57184145:57184145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5990C>T
AA Mutation	p.Ser1997Phe(p.S1997F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57138475:57138475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.84C>G
AA Mutation	p.Ser28Arg(p.S28R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57169170:57169170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3026C>A
AA Mutation	p.Ala1009Asp(p.A1009D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57179839:57179839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5024C>G
AA Mutation	p.Thr1675Arg(p.T1675R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57158449:57158449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1609A>G
AA Mutation	p.Ile537Val(p.I537V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57162407:57162407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2293G>T
AA Mutation	p.Val765Phe(p.V765F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57197332:57197332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9110A>G
AA Mutation	p.Tyr3037Cys(p.Y3037C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57211250:57211250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12991A>T
AA Mutation	p.Thr4331Ser(p.T4331S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57177521:57177521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4291G>T
AA Mutation	p.Gly1431Cys(p.G1431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000243077
Start	57200533:57200533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10106G>T
AA Mutation	p.Cys3369Phe(p.C3369F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000243077
Start	57205232:57205232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11318A>G
AA Mutation	p.Glu3773Gly(p.E3773G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243077
Start	57193198:57193198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7578A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243077
Start	57201092:57201092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551393670
CDS Mutation	c.10284C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243077
Start	57169288:57169288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373173236
CDS Mutation	c.3144C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243077
Start	57162440:57162440(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2331delC
AA Mutation	p.Thr778LeufsTer2(p.T778Lfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000243077
Start	57212151:57212151(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.13387delG
AA Mutation	p.Ala4463ProfsTer2(p.A4463Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript