Full data view for gene LRP5


Osteogenesis Imperfecta Variant Database
Information The variants shown are described using the NM_002335.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

Gender     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.1833dup r.(?) p.(Cys612ValfsTer25) Parent #1 - likely pathogenic (dominant) g.68174023dup g.68406555dup 1833dupG - LRP5_000315 - PubMed: Seo 2015 - - Germline - - - - - DNA SEQ - - retinal disease Pat16 PubMed: Seo 2015 - M - Korea - - - - - 1 LOVD
+/. - c.1833dupG r.(?) p.(Cys612Valfs*25) Maternal (confirmed) - pathogenic g.68174023dup g.68406555dup LRP5 c.1833dupG, p.(Cys612Valfs*25) - LRP5_000315 heterozygous PubMed: Maltese 2017 - - Germline yes - - - - DNA SEQ blood anna_tracewska EVR;FEVR, OPPG AB685 (Family 1) PubMed: Maltese 2017 family 1, individual A8685 (proband), 2 generation family, 2 affected M - Italy Italian - - - pars plana vitrectomy, laser photocoagulation 1 LOVD
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