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.

5 entries on 1 page. Showing entries 1 - 5.
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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)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/? 6 c.592G>A r.[592g>a, 471_592del] p.[Ala198Thr, Gly158Ilefs*9] Motor domain (1-729) Parent #2 ACMG likely pathogenic g.76867827G>A g.77156781G>A - - MYO7A_000072 Heterozygous; E6 skipping (Le Guédard-Méreuze , 2010) PubMed: Roux 2006 - - Germline - 0/664 controls -HpyAV - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Algeria - - - - - 1 Anne-Françoise Roux
+/? 6 c.592G>A r.[592g>a, 471_592del] p.[Ala198Thr, Gly158Ilefs*9] Motor domain (1-729) Parent #2 ACMG likely pathogenic g.76867827G>A g.77156781G>A - - MYO7A_000072 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. 6 c.592G>A r.(?) p.(Ala198Thr) - Maternal (confirmed) - likely pathogenic (recessive) g.76867827G>A - c.592G>A - MYO7A_000072 - PubMed: Khateb 2020 - - Germline yes - - - - DNA ? - - retinal disease CIC00417 PubMed: Khateb 2020 Two affected brothers M - - - - - - - 1 LOVD
+?/. 6 c.592G>A r.(?) p.(Ala198Thr) - Maternal (confirmed) - likely pathogenic (recessive) g.76867827G>A - c.592G>A p.Ala198Thr - MYO7A_000072 - PubMed: Khateb 2020 - - Germline yes - - - - DNA ? - - retinal disease CIC00418 PubMed: Khateb 2020 Two affected brothers M - - - - - - - 1 LOVD
+?/. 6 c.592G>A r.(?) p.(Ala198Thr) - Parent #2 - likely pathogenic (recessive) g.76867827G>A - c.592G>A p.Ala198Thr - MYO7A_000072 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC01199 PubMed: Khateb 2020 Two affected brothers M - - - - - - - 1 LOVD
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