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.

14 entries on 1 page. Showing entries 1 - 14.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

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Consanguinity     

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VIP     

Data_av     

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Panel size     

Owner     
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Parent #1 - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Heterozygous PubMed: Levy 1997 - rs121965079 Germline - - +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ - - USH1B ? PubMed: Levy 1997 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Homozygous Kahrizi et al., P49, 6th Molecular Biology of Hearing and Deafness Conference, 2007. - rs121965079 Germline - - +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ - - USH1B ? Kahrizi et al., P49, 6th Molecular Biology of Hearing and Deafness Conference, 2007. Proband - - Iran - - - - - 1 Anne-Françoise Roux
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Homozygous Kahrizi et al., P49, 6th Molecular Biology of Hearing and Deafness Conference, 2007. - rs121965079 Germline - - +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ - - USH1B ? Kahrizi et al., P49, 6th Molecular Biology of Hearing and Deafness Conference, 2007. Proband - - Iran - - - - - 1 Anne-Françoise Roux
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Parent #1 - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Heterozygous PubMed: Jaijo 2006 - rs121965079 Germline - - +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ - - USH1B ? PubMed: Jaijo 2006 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Homozygous PubMed: Kimberling 2010 - rs121965079 Germline - - +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ - - DFNB ? PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Maternal (inferred) - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Homozygous PubMed: Kimberling 2010 - rs121965079 Germline - - +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ - - DFNB ? PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Paternal (inferred) - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Heterozygous; probable pathogenic PubMed: Nakanishi 2010 - rs121965079 Germline - 0/64 controls +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ - - USH1B ? PubMed: Nakanishi 2010 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Parent #2 - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Heterozygous; mutation PubMed: Bonnet 2016 - rs121965079 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/+ 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Parent #1 - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 Heterozygous; mutation PubMed: Bonnet 2016 - rs121965079 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. 5 c.448C>T r.(?) p.(Arg150*) Motor domain (1-729) Parent #1 - pathogenic (recessive) g.76867115C>T - - - MYO7A_000129 - PubMed: Ivanova 2018 - rs121965079 Germline - - +PvuII;+DdeI;+BspCNI;+AluI;+MspA1I;-BcgI; - - DNA SEQ-NG-S - - USH1B Pat7 PubMed: Ivanova 2018 Proband F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+/. - c.448C>T r.(?) p.(Arg150*) - Parent #1 - pathogenic g.76867115C>T g.77156069C>T - - MYO7A_000129 8 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs121965079 Germline - 8/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 8 Mohammed Faruq
+/. - c.448C>T r.(?) p.(Arg150Ter) - Paternal (confirmed) ACMG pathogenic g.76867115C>T - - - MYO7A_000129 - PubMed: Mansard et al, 2021 - rs121965079 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. 5 c.448C>T r.(?) p.(Arg150*) - Parent #1 - likely pathogenic (recessive) g.76867115C>T - c.448C>T - MYO7A_000129 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06529 PubMed: Khateb 2020 one affected sister M - - Burkinabé - - - - 1 LOVD
+/. 5 c.448C>T r.(?) p.(Arg150*) - Parent #1 - pathogenic g.76867115C>T - c.448C>T - MYO7A_000129 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
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