Full data view for gene P3H1


Osteogenesis Imperfecta Variant Database
Information The variants shown are described using the NM_022356.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

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     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 1 c.26T>C r.(?) p.Leu9Pro Unknown - pathogenic g.43232617A>G - - - P3H1_000041 P3H1 sequence variants are normally recessive. The single variant in this patient probably does not account alone for the OI phenotype. PubMed: Mohd Nawawi 2018 - - Germline - - - - - DNA SEQ-NG - custom gene panel OI OI 10 PubMed: Mohd Nawawi 2018 - - - Malaysia - - - - - 1 Raymond Dalgleish
+/+ 1 c.26T>C r.(?) p.Leu9Pro Unknown - pathogenic g.43232617A>G - - - P3H1_000041 P3H1 sequence variants are normally recessive. The single variant in this patient probably does not account alone for the OI phenotype. PubMed: Mohd Nawawi 2018 - - Germline - - - - - DNA SEQ-NG - custom gene panel OI OI 14 PubMed: Mohd Nawawi 2018 - - - Malaysia - - - - - 1 Raymond Dalgleish
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.