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.

10 entries on 1 page. Showing entries 1 - 10.
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+/+ 7 c.721C>T r.(?) p.(Arg241Cys) Motor domain (1-729) Parent #1 - pathogenic g.76868036C>T g.77156990C>T - - MYO7A_000223 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/172 controls - - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 7 c.721C>T r.(?) p.(Arg241Cys) Motor domain (1-729) Unknown - pathogenic g.76868036C>T g.77156990C>T - - MYO7A_000223 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/172 controls - - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 7 c.721C>T r.(?) p.(Arg241Cys) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76868036C>T g.77156990C>T - - MYO7A_000223 Heterozygous; mutation PubMed: Zhai 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ, SEQ-NG-S - - USH2 ? PubMed: Zhai 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 7 c.721C>T r.(?) p.(Arg241Cys) Motor domain (1-729) Parent #2 - pathogenic g.76868036C>T g.77156990C>T - - MYO7A_000223 Heterozygous PubMed: Jiang 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/. - c.721C>T r.(?) p.(Arg241Cys) - Unknown - pathogenic (recessive) g.76868036C>T - 11:76868036C>T ENST00000409709.3:c.721C>T (Arg241Cys) - MYO7A_000223 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001025 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+/. - c.721C>T r.(?) p.(Arg241Cys) - Parent #1 ACMG pathogenic g.76868036C>T g.77156990C>T - - MYO7A_000223 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL 19147 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
+/. 7 c.721C>T r.(?) p.(Arg241Cys) - Parent #2 ACMG pathogenic (recessive) g.76868036C>T - - - MYO7A_000223 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1B Pat6 PubMed: Bahena 2021 - F no Iran - - - - - 1 Barbara Vona
+?/. - c.721C>T r.(?) p.(Arg241Cys) - Unknown - likely pathogenic g.76868036C>T g.77156990C>T MYO7A c.721C>T, p.Arg241Cys - MYO7A_000223 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001025 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+/. - c.721C>T r.(?) p.(Arg241Cys) - Unknown ACMG pathogenic g.76868036C>T g.77156990C>T MYO7A c.721C>T(;)3576G>A, V1: c.721C>T, (p.Arg241Cys) - MYO7A_000223 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F034 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+/. - c.721C>T r.(?) p.(Arg241Cys) - Unknown - pathogenic g.76868036C>T g.77156990C>T MYO7A c.721C>T(;)3576G>A; p.(Arg241Cys) - MYO7A_000223 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0; GnomAD_exome_East: 0; GnomAD_All: 0.0000121 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F034 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
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