Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

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     
-?/? 6i c.593-5C>T r.(=) p.(=) - Unknown ACMG likely benign g.76867903C>T g.77156857C>T - - MYO7A_000298 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs762666 Germline - 0/96 controls +PstI;+HpyCH4V;+SfcI;-AciI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 6i c.593-5C>T r.spl? p.? - Unknown ACMG likely benign g.76867903C>T g.77156857C>T - - MYO7A_000298 Heterozygous PubMed: Najera 2002 - rs762666 Germline - - +PstI;+HpyCH4V;+SfcI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Najera 2002 Proband F - Spain - - - - - 1 Jose Maria Millan
-?/? 6i c.593-5C>T r.spl? p.? - Unknown ACMG likely benign g.76867903C>T g.77156857C>T - - MYO7A_000298 Heterozygous PubMed: Roux 2011 - rs762666 Germline - - +PstI;+HpyCH4V;+SfcI;-AciI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
Legend   How to query  


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