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.

12 entries on 1 page. Showing entries 1 - 12.
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     
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Maternal (inferred) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous PubMed: Le Quesne Stabej 2012 - - Germline - 0/96 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Paternal (inferred) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous PubMed: Le Quesne Stabej 2012 - - Germline - 0/96 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Paternal (inferred) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous PubMed: Riazuddin 2008 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Maternal (inferred) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous PubMed: Riazuddin 2008 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Paternal (inferred) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous PubMed: Bonnet 2011 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Maternal (inferred) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous PubMed: Bonnet 2011 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Paternal (confirmed) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Maternal (confirmed) - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/+ 24 c.2914C>T r.(?) p.(Arg972*) - Parent #1 - pathogenic g.76893006C>T g.77181960C>T - - MYO7A_000244 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/. 24 c.2914C>T r.(?) p.(Arg972*) - Both (homozygous) ACMG pathogenic (recessive) g.76893006C>T - - - MYO7A_000244 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat16 PubMed: Bahena 2021 - M yes Iran - - - - - 1 Barbara Vona
+?/. - c.2914C>T r.(?) p.(Arg972*) - Unknown - likely pathogenic g.76893006C>T g.77181960C>T c.2914C>T p.(Arg972*) - MYO7A_000244 homozygous PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 038 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+/. - c.2914C>T r.(?) p.(Arg972Ter) - Paternal (confirmed) ACMG pathogenic g.76893006C>T - - - MYO7A_000244 - PubMed: Mansard et al, 2021 - rs782281371 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 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.