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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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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Owner     
+?/. - c.3546C>A r.(?) p.(Asn1182Lys) - Unknown - likely pathogenic g.76900431C>A g.77189386C>A MYO7A(NM_000260.3):c.3546C>A (p.N1182K), MYO7A(NM_000260.4):c.3546C>A (p.N1182K) - MYO7A_000581 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/? 28 c.3546C>A r.(?) p.(Asn1182Lys) MyTH4 1 (1017-1253) Paternal (confirmed) ACMG likely pathogenic g.76900431C>A g.77189386C>A - - MYO7A_000581 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/? 28 c.3546C>A r.(?) p.(Asn1182Lys) MyTH4 1 (1017-1253) Maternal (confirmed) ACMG likely pathogenic g.76900431C>A g.77189386C>A - - MYO7A_000581 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/. - c.3546C>A r.(?) p.(Asn1182Lys) - Unknown - likely pathogenic g.76900431C>A g.77189386C>A MYO7A(NM_000260.3):c.3546C>A (p.N1182K), MYO7A(NM_000260.4):c.3546C>A (p.N1182K) - MYO7A_000581 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.3546C>A r.(?) p.(Asn1182Lys) - Unknown - VUS g.76900431C>A g.77189386C>A MYO7A(NM_000260.3):c.3546C>A (p.N1182K), MYO7A(NM_000260.4):c.3546C>A (p.N1182K) - MYO7A_000581 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.3546C>A r.(?) p.(Asn1182Lys) - Unknown - pathogenic (recessive) g.76900431C>A - 11:76900431C>A ENST00000409709.3:c.3546C>A (Asn1182Lys) - MYO7A_000581 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001025 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.3546C>A r.(?) p.(Asn1182Lys) - Unknown - likely pathogenic g.76900431C>A g.77189386C>A MYO7A c.3546C>A, p.Asn1182Lys - MYO7A_000581 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
+?/. 28 c.3546C>A r.(?) p.(Asn1182Lys) - Both (homozygous) - likely pathogenic (recessive) g.76900431C>A - c.3546C>A p.Asn1182Lys - MYO7A_000581 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC00072 PubMed: Khateb 2020 one affected brother F - - French - - - - 1 LOVD
+?/. 28 c.3546C>A r.(?) p.(Asn1182Lys) - Both (homozygous) - likely pathogenic (recessive) g.76900431C>A - c.3546C>A p.Asn1182Lys - MYO7A_000581 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC00071 PubMed: Khateb 2020 one affected sister M - - French - - - - 1 LOVD
+?/. - c.3546C>A r.(?) p.(Asn1182Lys) - Unknown - likely pathogenic g.76900431C>A - MYO7A(NM_000260.3):c.3546C>A (p.N1182K), MYO7A(NM_000260.4):c.3546C>A (p.N1182K) - MYO7A_000581 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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