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     
+/? 5 c.682G>A r.(?) p.(Gly228Arg) PDZ 2 (210-293) Both (homozygous) ACMG VUS g.102782003C>T g.101022246C>T - - PDZD7_000015 {MSV3dQ9UKN7:p.Gly228Arg} PubMed: Booth 2015 - - Germline - 0/600 controls - - - DNA SEQ, SEQ-NG-S - - deafness FamL-8900092PatII1 PubMed: Booth 2015 2-generation family, 3 affected sibs (2F, M), unaffected heterozygous carrier parents M - Iran - - - - - 3 Anne-Françoise Roux
+/? 5 c.682G>A r.(?) p.(Gly228Arg) PDZ 2 (210-293) Both (homozygous) ACMG VUS g.102782003C>T g.101022246C>T - - PDZD7_000015 {MSV3dQ9UKN7:p.Gly228Arg} PubMed: Booth 2015 - - Germline - 0/600 controls - - - DNA SEQ, SEQ-NG-S - - deafness FamL-8900092PatII2 PubMed: Booth 2015 sister F - Iran - - - - - 1 Anne-Françoise Roux
+/? 5 c.682G>A r.(?) p.(Gly228Arg) PDZ 2 (210-293) Both (homozygous) ACMG VUS g.102782003C>T g.101022246C>T - - PDZD7_000015 {MSV3dQ9UKN7:p.Gly228Arg} PubMed: Booth 2015 - - Germline - 0/600 controls - - - DNA SEQ, SEQ-NG-S - - deafness FamL-8900092PatII3 PubMed: Booth 2015 sister F - Iran - - - - - 1 Anne-Françoise Roux
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