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     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ClinVar ID     

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Owner     
+/+ 32 c.4293G>A r.(?) p.(Trp1431*) FERM 1 (1258-1602) Maternal (confirmed) - pathogenic g.76905539G>A g.77194494G>A - - MYO7A_000321 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -NlaIV;-ApaI;-BaeGI;-PspOMI;-HaeIII;-SfiI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
?/. - c.4293G>A r.(?) p.(Trp1431*) - Unknown - VUS g.76905539G>A g.77194494G>A MYO7A nucleotide 1, protein 1:c.4293G>A, p.Trp1431* nucleotide 2, protein 2:c.5916G>A, p.Trp1972* - MYO7A_000321 heterozygous, ACMG unclassified - no access to supplementary 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
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