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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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

Methylation     

Template     

Technique     

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Disease     

ID_report     

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Owner     
+/+ 4 c.223del r.(?) p.(Asp75Thrfs*31) Motor domain (1-729) Unknown - pathogenic g.76858934del g.77147888del 223delG - MYO7A_000001 Heterozygous PubMed: Weston 1996 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - Algeria - - - - - 1 William J. Kimberling
+/+ 4 c.223del r.(?) p.(Asp75Thrfs*31) Motor domain (1-729) Parent #1 - pathogenic g.76858934del g.77147888del 223delG - MYO7A_000001 Heterozygous PubMed: Roux 2006 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 4 c.223del r.(?) p.(Asp75Thrfs*31) Motor domain (1-729) Parent #1 - pathogenic g.76858934del g.77147888del 223delG - MYO7A_000001 Heterozygous PubMed: Roux 2006 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 4 c.223del r.(?) p.(Asp75Thrfs*31) Motor domain (1-729) Parent #1 - pathogenic g.76858934del g.77147888del 223delG - MYO7A_000001 Heterozygous PubMed: Maubaret 2005 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Maubaret 2005 Proband - - France - - - - - 1 Anne-Françoise Roux
+/+ 4 c.223del r.(?) p.(Asp75Thrfs*31) Motor domain (1-729) Unknown - pathogenic g.76858934del g.77147888del 223delG - MYO7A_000001 Heterozygous PubMed: Bharadwaj 2000 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+?/. 4 c.223del r.(?) p.(Asp75Thrfs*31) - Maternal (confirmed) - likely pathogenic (recessive) g.76858934del - c.223del p.Asp75Thrfs*31 - MYO7A_000001 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC02640 PubMed: Khateb 2020 simplex case M - - French - - - - 1 LOVD
+?/. 4 c.223del r.(?) p.(Asp75Thrfs*31) - Parent #1 - likely pathogenic (recessive) g.76858934del - c.223del - MYO7A_000001 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1571135 PubMed: Khateb 2020 - F - - - - - - - 1 LOVD
+/. - c.223delG r.(?) p.(Asp75ThrfsTer31) - Paternal (confirmed) ACMG pathogenic g.76858934del - - - MYO7A_000001 - PubMed: Mansard et al, 2021 - rs876657415 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
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