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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+?/? 39 c.5434G>A r.(?) p.(Glu1812Lys) MyTH4 2 (1747-1896) Paternal (inferred) ACMG VUS g.76915228G>A g.77204183G>A - - MYO7A_000267 Homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Tunisia - - - - - 1 Anne-Françoise Roux
+/? 39 c.5434G>A r.(?) p.(Glu1812Lys) MyTH4 2 (1747-1896) Maternal (inferred) ACMG VUS g.76915228G>A g.77204183G>A - - MYO7A_000267 Homozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Tunisia - - - - - 1 Anne-Françoise Roux
+?/? 39 c.5434G>A r.(?) p.(Glu1812Lys) MyTH4 2 (1747-1896) Paternal (inferred) ACMG VUS g.76915228G>A g.77204183G>A - - MYO7A_000267 Homozygous; likely pathogenic PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/? 39 c.5434G>A r.(?) p.(Glu1812Lys) MyTH4 2 (1747-1896) Maternal (inferred) ACMG VUS g.76915228G>A g.77204183G>A - - MYO7A_000267 Homozygous; likely pathogenic PubMed: Glöcke 2013; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Glöcke 2013 Proband - - - - - - - - 1 Anne-Françoise Roux
+/. - c.5434G>A r.(?) p.(Glu1812Lys) - Both (homozygous) - pathogenic (recessive) g.76915228G>A g.77204183G>A - - MYO7A_000267 - PubMed: Riahi 2015 - - Germline yes - - - - DNA SEQ-NG - WES deafness FamDF103 PubMed: Riahi 2015 3-generation family, affected (F), unaffected parents F;M yes Tunisia - - - - - 2 LOVD
?/. - c.5434G>A r.(?) p.(Glu1812Lys) - Unknown - VUS g.76915228G>A g.77204183G>A MYO7A c.5434G>A, p.Glu1812Lys - MYO7A_000267 unsolved PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2846_004431 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+?/. - c.5434G>A r.(?) p.(Glu1812Lys) - Parent #1 - likely pathogenic g.76915228G>A g.77204183G>A MYO7A, variant 1: c.5434G>A/p.E1812K, variant 2: c.5434G>A/p.E1812K - MYO7A_000267 solved, homozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET1 targeted sequencing panel - see paper retinal disease 75 PubMed: Weisschuh 2020 Filing key number: 38, Usher syndrome type I, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.5434G>A r.(?) p.(Glu1812Lys) - Both (homozygous) - pathogenic (recessive) g.76915228G>A g.77204183G>A - - MYO7A_000267 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4206 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
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