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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+/. 20 c.2307del r.(?) p.(Asn769Lysfs*5) - Both (homozygous) - pathogenic g.76890115del g.77179069del - - MYO7A_000501 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F no Israel Arab-Muslim - - - - 2 Dror Sharon
+/+ 20 c.2307del r.(?) p.(Asn769Lysfs*5) IQ 2 (768-788) Paternal (inferred) - pathogenic g.76890115del g.77179069del 2308delC - MYO7A_000501 Homozygous PubMed: Goldenberg-Cohen 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Goldenberg-Cohen 2013 Proband F - Israel - - - - - 1 Anne-Françoise Roux
+/+ 20 c.2307del r.(?) p.(Asn769Lysfs*5) IQ 2 (768-788) Maternal (inferred) - pathogenic g.76890115del g.77179069del 2308delC - MYO7A_000501 Homozygous PubMed: Goldenberg-Cohen 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Goldenberg-Cohen 2013 Proband F - Israel - - - - - 1 Anne-Françoise Roux
+/+ 20 c.2307del r.(?) p.(Asn769Lysfs*5) IQ 2 (768-788) Paternal (inferred) - pathogenic g.76890115del g.77179069del 2308delC - This patient also carries homozygous mutation 1417delC in PDE6B - MYO7A_000501 Homozygous PubMed: Goldenberg-Cohen 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Goldenberg-Cohen 2013 Proband M - Israel - - - - - 1 Anne-Françoise Roux
+/+ 20 c.2307del r.(?) p.(Asn769Lysfs*5) IQ 2 (768-788) Maternal (inferred) - pathogenic g.76890115del g.77179069del 2308delC - This patient also carries homozygous mutation 1417delC in PDE6B - MYO7A_000501 Homozygous PubMed: Goldenberg-Cohen 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Goldenberg-Cohen 2013 Proband M - Israel - - - - - 1 Anne-Françoise Roux
+/. - c.2307del r.(?) p.(Asn769Lysfs*5) - Unknown ACMG pathogenic g.76890115del - c.2307delC - MYO7A_000501 - PubMed: Sharon 2019 - - Germline - 2/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - 2 Global Variome, with Curator vacancy
?/. 20 c.2307del r.(?) p.(Asn769Lysfs*5) - Unknown - VUS g.76890115del - c.2307delC - MYO7A_000501 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA arraySNP, SEQ-NG blood WES retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
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