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     
+?/. - c.490C>T r.(?) p.(Arg164Trp) - Both (homozygous) ACMG likely pathogenic (recessive) g.102783245G>A g.101023488G>A - - PDZD7_000060 ACMG PM2, PM3_P, PP1, PP3 PubMed: Kim 2020, Journal: Kim 2020 - - Germline - - - - - DNA SEQ-NG-I - - deafness SB78-137 PubMed: Kim 2020, Journal: Kim 2020 - - - Korea - - - - - 1 Doo-Yi Oh
+?/. - c.490C>T r.(?) p.(Arg164Trp) - Both (homozygous) - VUS g.102783245G>A g.101023488G>A - - PDZD7_000060 - - - - Germline ? - - - - DNA SEQ-NG-I whole blood WES deafness SB297-597 - - F ? Korea, South (Republic) Asian 00y05m - - - 1 Seungmin Lee
?/. - c.490C>T r.(?) p.(Arg164Trp) - Unknown - VUS g.102783245G>A - - - PDZD7_000060 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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