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.

4 entries on 1 page. Showing entries 1 - 4.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 14i c.1690+1G>A r.spl p.? - Parent #1 - pathogenic g.76874035G>A g.77162989G>A - - MYO7A_000366 Heterozygous PubMed: Bonnet 2011 - rs111033389 Germline - - -CviQI;-BsaJI;-StyI;-RsaI; - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 14i c.1690+1G>A r.spl p.? - Parent #2 - pathogenic g.76874035G>A g.77162989G>A - - MYO7A_000366 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033389 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/. - c.1690+1G>A r.(?) p.(?) - Maternal (confirmed) ACMG pathogenic g.76874035G>A - - - MYO7A_000366 - PubMed: Mansard et al, 2021 - rs111033389 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 14i c.1690+1G>A r.spl? p.? - Parent #1 - likely pathogenic (recessive) g.76874035G>A - c.1690+1G>A - MYO7A_000366 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1366491 PubMed: Khateb 2020 simplex case F - - French - - - - 1 LOVD
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