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.

9 entries on 1 page. Showing entries 1 - 9.
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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     

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Template     

Technique     

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Disease     

ID_report     

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Owner     
+/. - c.1555-8C>G r.(=) p.(=) - Unknown - pathogenic g.76873891C>G g.77162845C>G - - MYO7A_000105 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/? 13i c.1555-8C>G r.[(1554_1555ins1555-7_1555-1, 1555_1690del)] p.([Gly519Serfs*27, Gly519Alafs*58]) Motor domain (1-729) Parent #2 ACMG likely pathogenic g.76873891C>G g.77162845C>G - - MYO7A_000105 Heterozygous; ins last 7 nt IVS13 + skipping E14 (Le Guédard-Méreuze , 2010) PubMed: Roux 2006 - - Germline - 0/100 controls +BpmI;+BsrI;+BsmFI; - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2006 Proband F - France - - - - - 1 Anne-Françoise Roux
+/? 13i c.1555-8C>G r.[1554_1555ins1555-7_1555-1, 1555_1690del] p.[Gly519Serfs*27, Gly519Alafs*58] Motor domain (1-729) Parent #2 ACMG likely pathogenic g.76873891C>G g.77162845C>G - - MYO7A_000105 Heterozygous; ins last 7 nt IVS13 + skipping E14 PubMed: Le Guédard-Méreuze 2010 - - Germline - 0/200 controls +BpmI;+BsrI;+BsmFI; - - DNA minigene, SEQ - - USH1B ? PubMed: Le Guédard-Méreuze 2010 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 13i c.1555-8C>G r.[1554_1555ins1555-7_1555-1, 1555_1690del] p.[Gly519Serfs*27, Gly519Alafs*58] Motor domain (1-729) Parent #1 ACMG likely pathogenic g.76873891C>G g.77162845C>G - - MYO7A_000105 Heterozygous; ins last 7 nt IVS13 + skipping E14 PubMed: Roux 2011 - - Germline - 0/200 controls +BpmI;+BsrI;+BsmFI; - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+/? 13i c.1555-8C>G r.[(1554_1555ins1555-7_1555-1, 1555_1690del)] p.[(Gly519Serfs*27, Gly519Alafs*58)] Motor domain (1-729) Parent #2 ACMG likely pathogenic g.76873891C>G g.77162845C>G - - MYO7A_000105 Heterozygous PubMed: Weston 1996 - - Germline - - +BpmI;+BsrI;+BsmFI; - - DNA SEQ - - USH1B ? PubMed: Weston 1996 Proband - - United States - - - - - 1 William J. Kimberling
+/? 13i c.1555-8C>G r.[(1554_1555ins1555-7_1555-1, 1555_1690del)] p.([Gly519Serfs*27, Gly519Alafs*58]) Motor domain (1-729) Unknown ACMG likely pathogenic g.76873891C>G g.77162845C>G - - MYO7A_000105 Heterozygous; ins last 7 nt IVS13 + skipping E14 (Le Guédard-Méreuze , 2010) PubMed: Roux 2011 - - Germline - 0/100 controls +BpmI;+BsrI;+BsmFI; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. 13i c.1555-8C>G r.spl p.? - Parent #1 - pathogenic g.76873891C>G g.77162845C>G 1555-8C>G (IVS13-8C>G) - MYO7A_000105 unknown variant 2nd chromosome PubMed: Cremers 2007 - - Germline - - - - - DNA SEQ - - retinal disease USH1-10 PubMed: Cremers 2007 - M no Denmark - - - - - 1 LOVD
+?/. 13i c.1555-8C>G r.(=) p.(=) - Both (homozygous) - likely pathogenic g.76873891C>G - c.1555-8C>G - MYO7A_000105 - PubMed: Colombo-2020 - rs1057517774 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+?/. 13i c.1555-8C>G r.(=) p.(=) - Parent #1 - likely pathogenic (recessive) g.76873891C>G - c.1555-8C>G - MYO7A_000105 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1617688 PubMed: Khateb 2020 simplex case F - - French - - - - 1 LOVD
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