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     
+/+ 14 c.2107del r.(?) p.(Ser703Valfs*20) - Maternal (confirmed) ACMG pathogenic g.102770540del g.101010783del - - PDZD7_000011 - PubMed: Vona et al., 2016 - rs397516633 Germline - - - - - DNA SEQ-NG-S - - deafness - PubMed: Vona et al., 2016 Proband - Autosomal recessive deafness - - - - - - - - 1 Barbara Vona
+/. - c.2107del r.(?) p.(Ser703ValfsTer20) - Unknown - pathogenic g.102770540del g.101010783del PDZD7(NM_001195263.1):c.2107delA (p.S703Vfs*20) - PDZD7_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.2107del r.(?) p.(Ser703ValfsTer20) - Unknown - pathogenic g.102770540del - PDZD7(NM_001195263.1):c.2107delA (p.S703Vfs*20) - PDZD7_000011 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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