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     

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VIP     

Data_av     

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Owner     
+/+ 43 c.5916G>A r.(?) p.(Trp1972*) FERM2 (1902-2205) Parent #1 - pathogenic g.76919534G>A g.77208489G>A - - MYO7A_000563 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.5916G>A r.(?) p.(Trp1972*) - Unknown ACMG likely pathogenic g.76919534G>A g.77208489G>A MYO7A nucleotide 1, protein 1:c.4293G>A, p.Trp1431* nucleotide 2, protein 2:c.5916G>A, p.Trp1972* - MYO7A_000563 heterozygous, ACMG classified, novel (Table 2) PubMed: Hull 2020 - - Germline ? - - - - DNA ? blood NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families retinal disease 76 PubMed: Hull 2020 - ? - New Zealand white - - - - 1 LOVD
+?/. 43 c.5916G>A r.(?) p.(Trp1972*) - Parent #1 - likely pathogenic (recessive) g.76919534G>A - c.5916G>A - MYO7A_000563 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08846 PubMed: Khateb 2020 one affected sister M - - French - - - - 1 LOVD
+?/. 43 c.5916G>A r.(?) p.(Trp1972*) - Parent #1 - likely pathogenic (recessive) g.76919534G>A - c.5916G>A - MYO7A_000563 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06731 PubMed: Khateb 2020 one affected brother F - - French - - - - 1 LOVD
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