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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+/+ 12 c.1258A>T r.(?) p.(Lys420*) Motor domain (1-729) Unknown - pathogenic g.76872076A>T g.77161030A>T - - MYO7A_000329 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - - +BfaI - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 12 c.1258A>T r.(?) p.(Lys420*) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76872076A>T g.77161030A>T - - MYO7A_000329 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 12 c.1258A>T r.(?) p.(Lys420*) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76872076A>T g.77161030A>T - - MYO7A_000329 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.1258A>T r.(?) p.(Lys420*) - Unknown ACMG pathogenic g.76872076A>T - - - MYO7A_000329 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+/. - c.1258A>T r.(?) p.(Lys420*) - Both (homozygous) - pathogenic (recessive) g.76872076A>T g.77161030A>T - - MYO7A_000329 - PubMed: Chen 2018 - - Germline - - - - - DNA SEQ - - HL FamJ03 PubMed: Chen 2018 - - - China Uyghur - - - - 1 LOVD
+?/. 12 c.1258A>T r.(?) p.(Lys420*) - Both (homozygous) - likely pathogenic (recessive) g.76872076A>T - c.1258A>T - MYO7A_000329 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08356 PubMed: Khateb 2020 simplex case F yes - German - - - - 1 LOVD
+/. - c.1258A>T r.(?) p.(Lys420Ter) - Parent #1 - pathogenic (recessive) g.76872076A>T g.77161030A>T - - MYO7A_000329 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4190 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.1258A>T r.(?) p.(Lys420Ter) - Paternal (confirmed) - pathogenic (recessive) g.76872076A>T g.77161030A>T - - MYO7A_000329 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4652 PubMed: Richard 2019 4-generation family, 3 affected sibs (F, 2M) - yes Pakistan - - - - - 3 Johan den Dunnen
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