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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.1849T>C r.(?) p.(Ser617Pro) - Unknown - pathogenic g.76883845T>C g.77172799T>C - - MYO7A_000711 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.1849T>C r.(?) p.(Ser617Pro) - Unknown - pathogenic (recessive) g.76883845T>C - 11:76883845T>C ENST00000409709.3:c.1849T>C (Ser617Pro) - MYO7A_000711 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001031 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Asia-South - - - - 1 LOVD
+?/. - c.1849T>C r.(?) p.(Ser617Pro) - Unknown - likely pathogenic g.76883845T>C g.77172799T>C MYO7A c.1849T>C, p.Ser617Pro - MYO7A_000711 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001031 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.1849T>C r.(?) p.(Ser617Pro) - Maternal (confirmed) - pathogenic (recessive) g.76883845T>C g.77172799T>C - - MYO7A_000711 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL PKDF019A PubMed: Richard 2019 2-generation family, 5 affected (3F, 2M) - yes Pakistan - - - - - 5 Johan den Dunnen
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