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.

2 entries on 1 page. Showing entries 1 - 2.
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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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+?/. - c.22dup r.(?) p.(Asp8Glyfs*34) - Unknown - likely pathogenic g.76853758dup g.77142712dup MYO7A c.22dupG, p.Asp8GlyfsTer34 - MYO7A_001035 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G006299 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.22dup r.(?) p.(Asp8Glyfs*34) - Unknown - likely pathogenic g.76853758dup g.77142712dup MYO7A c.22dupG, p.Asp8Glyfs*34 - MYO7A_001035 - PubMed: Georgiou 2021 - - Unknown ? - - - - DNA SEQ-NG blood retrospective study retinal disease P8 PubMed: Georgiou 2021 pedigree ID: 19131, genetic ID: 29686 M - (United Kingdom (Great Britain)) - - - - - 1 LOVD
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