Mutation

Primary Site >> Liver Cancer

Gene >> LRP2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169201774:169201774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8306G>C
AA Mutation	p.Gly2769Ala(p.G2769A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263816
Start	169244695:169244695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3428G>T
AA Mutation	p.Cys1143Phe(p.C1143F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169202812:169202812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8153A>G
AA Mutation	p.Lys2718Arg(p.K2718R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169146875:169146875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12675C>A
AA Mutation	p.Phe4225Leu(p.F4225L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169145858:169145858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.12877G>C
AA Mutation	p.Glu4293Gln(p.E4293Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169175274:169175274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745375377
CDS Mutation	c.10687G>A
AA Mutation	p.Gly3563Ser(p.G3563S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169207008:169207008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764132183
CDS Mutation	c.6712G>A
AA Mutation	p.Gly2238Ser(p.G2238S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169188092:169188092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.9206A>T
AA Mutation	p.His3069Leu(p.H3069L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169246855:169246855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781041064
CDS Mutation	c.3040G>A
AA Mutation	p.Glu1014Lys(p.E1014K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169216372:169216372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5707G>A
AA Mutation	p.Ala1903Thr(p.A1903T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169279492:169279492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445A>G
AA Mutation	p.Tyr482Cys(p.Y482C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169201804:169201804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8276G>T
AA Mutation	p.Arg2759Leu(p.R2759L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169201648:169201648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8432C>A
AA Mutation	p.Thr2811Asn(p.T2811N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169290977:169290977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790C>T
AA Mutation	p.His264Tyr(p.H264Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263816
Start	169242986:169242986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3637T>G
AA Mutation	p.Cys1213Gly(p.C1213G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263816
Start	169198841:169198841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8523G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263816
Start	169241163:169241163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3870T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263816
Start	169173169:169173169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11070C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	splice_acceptor_variant;intron_variant
Transcription ID	ENST00000263816
Start	169176589:169176600(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.10394-12_10394-1delCTTTTCCACTAG
Mutation Classification	Splice_Site
Feature Type	Transcript