Full data view for gene PDZD7


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_001195263.1 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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     
-/? 15 c.2144C>T r.(?) p.(Pro715Leu) - Unknown ACMG likely benign g.102770502G>A g.101010745G>A - - PDZD7_000006 {MSV3dQ9UKN7:p.Pro715Leu} PubMed: Besnard, Garcia-Garcia et al., 2014 - rs143414291 Germline - - - - - DNA SEQ-NG-S, Southern - - USH2 - PubMed: Besnard, Garcia-Garcia et al., 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/. - c.2144C>T r.(?) p.(Pro715Leu) - Unknown - benign g.102770502G>A g.101010745G>A PDZD7(NM_001195263.1):c.2144C>T (p.P715L), PDZD7(NM_001195263.2):c.2144C>T (p.P715L) - PDZD7_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.2144C>T r.(?) p.(Pro715Leu) - Unknown - likely benign g.102770502G>A g.101010745G>A PDZD7(NM_001195263.1):c.2144C>T (p.P715L), PDZD7(NM_001195263.2):c.2144C>T (p.P715L) - PDZD7_000006 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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