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.

18 entries on 1 page. Showing entries 1 - 18.
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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     

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Consanguinity     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.5944G>A r.(?) p.(Gly1982Arg) - Unknown - pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/? 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Maternal (confirmed) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/? 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Unknown ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/? 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Paternal (inferred) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous PubMed: Riazuddin 2008 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/? 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Maternal (inferred) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous PubMed: Riazuddin 2008 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/? 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Paternal (inferred) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous PubMed: Riazuddin 2008 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Maternal (inferred) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous PubMed: Riazuddin 2008 - - Germline - - none - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/? 43 c.5944G>A r.5857_5944del p.Val1953Glufs*12 FERM 2 (1902-2205) Parent #2 ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Heterozygous; E43 skipping PubMed: Roux 2011 - - Germline - 0/200 controls none - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 43 c.5944G>A r.5857_5944del p.Val1953Glufs*12 FERM 2 (1902-2205) Parent #2 ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Heterozygous; E43 skipping PubMed: Le Guédard-Méreuze 2010 - - Germline - 0/200 controls none - - DNA minigene, SEQ - - USH1B ? PubMed: Le Guédard-Méreuze 2010 Relative M - France - - - - - 1 Anne-Françoise Roux
+/? 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Paternal (inferred) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous PubMed: Aparisi 2014 - - Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/? 43 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Maternal (inferred) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous PubMed: Aparisi 2014 - - Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/? 44 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Maternal (confirmed) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous; mutation PubMed: Bonnet 2016 - rs761469964 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/? 44 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Paternal (confirmed) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous; mutation PubMed: Bonnet 2016 - rs761469964 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/? 44 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Paternal (confirmed) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous; mutation PubMed: Bonnet 2016 - rs761469964 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/? 44 c.5944G>A r.(5857_5944del) p.(Val1953Glufs*12) FERM 2 (1902-2205) Maternal (confirmed) ACMG likely pathogenic g.76919562G>A g.77208517G>A - - MYO7A_000239 Homozygous; mutation PubMed: Bonnet 2016 - rs761469964 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/. 43 c.5944G>A r.(?) p.(Gly1982Arg) - Both (homozygous) - pathogenic (recessive) g.76919562G>A - c.5944G>A p.Gly1982Arg - MYO7A_000239 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC04838 PubMed: Khateb 2020 One affected sister M - - - - - - - 1 LOVD
+?/. 43 c.5944G>A r.(?) p.(Gly1982Arg) - Both (homozygous) - likely pathogenic (recessive) g.76919562G>A - c.5944G>A - MYO7A_000239 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC04837 PubMed: Khateb 2020 One affected brother F - - - - - - - 1 LOVD
+/. 43 c.5944G>A r.(?) p.(Gly1982Arg) - Both (homozygous) - pathogenic g.76919562G>A - c.5944G>A - MYO7A_000239 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
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