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     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.5886_5888del r.(?) p.(Phe1963del) - Both (homozygous) ACMG pathogenic g.76919504_76919506del g.77208459_77208461del - - MYO7A_000022 - PubMed: Trujillano 2017 - - Germline - - - - - DNA SEQ, SEQ-NG - - USH1 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - 1 Daniel Trujillano
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Maternal (inferred) ACMG VUS g.76919504_76919506del g.77208459_77208461del - - MYO7A_000022 Homozygous; UV4 PubMed: Le Quesne Stabej 2012 - rs111033232 Germline - 0/96 controls -MboII - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Paternal (inferred) ACMG VUS g.76919504_76919506del g.77208459_77208461del - - MYO7A_000022 Homozygous; UV4 PubMed: Le Quesne Stabej 2012 - rs111033232 Germline - 0/96 controls -MboII - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Parent #1 ACMG VUS g.76919504_76919506del g.77208459_77208461del 5886_5888delCTT - MYO7A_000022 Heterozygous PubMed: Roux 2006 - rs111033232 Germline - - -MboII - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Unknown ACMG VUS g.76919504_76919506del g.77208459_77208461del 5886_5888delCTT - MYO7A_000022 Heterozygous PubMed: Roux 2011 - rs111033232 Germline - - -MboII - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Paternal (inferred) ACMG VUS g.76919504_76919506del g.77208459_77208461del 5886_5888delCTT - MYO7A_000022 Homozygous PubMed: Roux 2011 - rs111033232 Germline - - -MboII - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Pakistan - - - - - 1 Anne-Françoise Roux
+/+ 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Maternal (inferred) ACMG VUS g.76919504_76919506del g.77208459_77208461del 5886_5888delCTT - MYO7A_000022 Homozygous PubMed: Roux 2011 - rs111033232 Germline - - -MboII - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Pakistan - - - - - 1 Anne-Françoise Roux
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Parent #2 ACMG VUS g.76919504_76919506del g.77208459_77208461del 5887_5889delTTC - p.F1963del - MYO7A_000022 Heterozygous; Presumably pathogenic PubMed: Bonnet 2011 - rs111033232 Germline - - -MboII - - DNA SEQ - - USH1B ? PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Parent #1 ACMG VUS g.76919504_76919506del g.77208459_77208461del NM_001127180:5766_5768del - p.1922_1923del - MYO7A_000022 Heterozygous; mutation PubMed: Jiang 2015 - rs111033232 Germline - - -MboII - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Paternal (inferred) ACMG VUS g.76919504_76919506del g.77208459_77208461del NM_001127180:5766_5768del - p.1922_1923del - MYO7A_000022 Homozygous; mutation PubMed: Jiang 2015 - rs111033232 Germline - - -MboII - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+?/? 43 c.5886_5888del r.(?) p.(Phe1963del) FERM 2 (1902-2205) Maternal (inferred) ACMG VUS g.76919504_76919506del g.77208459_77208461del NM_001127180:5766_5768del - p.1922_1923del - MYO7A_000022 Homozygous; mutation PubMed: Jiang 2015 - rs111033232 Germline - - -MboII - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+?/+ 43 c.5886_5888del r.(?) p.(Phe1963del) FERM2 (1902-2205) Parent #2 ACMG VUS g.76919504_76919506del g.77208459_77208461del 5886_5888delCTT - MYO7A_000022 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033232 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+?/+ 43 c.5886_5888del r.(?) p.(Phe1963del) FERM2 (1902-2205) Unknown ACMG VUS g.76919504_76919506del g.77208459_77208461del 5886_5888delCTT - MYO7A_000022 Heterozygous; mutation PubMed: Bonnet 2016 - rs111033232 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.5886_5888del r.(?) p.(Phe1963del) - Parent #2 - likely pathogenic (recessive) g.76919504_76919506del g.77208459_77208461del - - MYO7A_000022 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam5PatTO6 PubMed: Eandi 2017 - M - Italy - - - - - 1 LOVD
+?/. - c.5886_5888del r.(?) p.(Phe1963del) - Parent #2 - likely pathogenic g.76919504_76919506del g.77208459_77208461del - - MYO7A_000022 - PubMed: Riera 2017 - - Germline yes - - - - DNA SEQ-NG - 212-gene panel retinal disease Fi15/35 PubMed: Riera 2017 family, several affected - - Spain - - - - - 2 LOVD
+/. - c.5886_5888del r.(?) p.(Phe1963del) - Both (homozygous) - pathogenic g.76919504_76919506del g.77208459_77208461del - - MYO7A_000022 - PubMed: Neuhaus 2017 - rs111033232 Germline - - - - - DNA SEQ-NG - gene panel USH Pat90 PubMed: Neuhaus 2017 - - yes Saudi Arabia - - - - - 1 LOVD
+?/. 43 c.5886_5888del r.(?) p.(Phe1965del) - Unknown - likely pathogenic g.76919504_76919506del - c.5886_5888del - MYO7A_000022 - PubMed: Colombo-2020 - rs111033232 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+?/. 43 c.5886_5888del r.(?) p.(Phe1963del) - Parent #2 - likely pathogenic (recessive) g.76919504_76919506del - c.5886_5888del - MYO7A_000022 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1366491 PubMed: Khateb 2020 simplex case F - - French - - - - 1 LOVD
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