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.

37 entries on 1 page. Showing entries 1 - 37.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

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Re-site     

VIP     

Methylation     

Template     

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Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

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Consanguinity     

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VIP     

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?/. - c.2476G>A r.(?) p.(Ala826Thr) - Unknown - VUS g.76890889G>A g.77179843G>A MYO7A(NM_000260.3):c.2476G>A (p.A826T) - MYO7A_000013 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (confirmed) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/+ 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (confirmed) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (confirmed) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Heterozygous; UV4 PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 2/840 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Algeria - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Algeria - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Unknown ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Heterozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Algeria - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Relative - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Parent #2 ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Heterozygous PubMed: Adato 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Adato 1997 Proband - - Morocco - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Paternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Riazuddin 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+?/? 21 c.2476G>A r.(?) p.(Ala826Thr) IQ 4 (814-834) Maternal (inferred) ACMG VUS g.76890889G>A g.77179843G>A - - MYO7A_000013 Homozygous PubMed: Riazuddin 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - -BstUI;-HinP1I;-HhaI; - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+?/. - c.2476G>A r.(?) p.(Ala826Thr) - Unknown ACMG likely pathogenic g.76890889G>A - - - MYO7A_000013 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
?/. 21 c.2476G>A r.(?) p.(Ala826Thr) - Unknown - VUS g.76890889G>A - c.2476G>A - MYO7A_000013 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA arraySNP blood SNP-mutation screen retinal disease - PubMed: Khalaileh-2018 - - yes - North African Jew - - - - 1 LOVD
?/. 21 c.2476G>A r.(?) p.(Ala826Thr) - Unknown - VUS g.76890889G>A - c.2476G>A - MYO7A_000013 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - North African Jew - - - - 1 LOVD
+?/. 21 c.2476G>A r.(?) p.(Ala826Thr) - Both (homozygous) - likely pathogenic (recessive) g.76890889G>A - c.2476G>A p.Ala826Thr - MYO7A_000013 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC02732 PubMed: Khateb 2020 Two affected sisters F - - - - - - - 1 LOVD
+?/. 21 c.2476G>A r.(?) p.(Ala826Thr) - Both (homozygous) - likely pathogenic (recessive) g.76890889G>A - c.2476G>A p.Ala826Thr - MYO7A_000013 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC02730 PubMed: Khateb 2020 Two affected sisters F - - - - - - - 1 LOVD
+?/. 21 c.2476G>A r.(?) p.(Ala826Thr) - Both (homozygous) - likely pathogenic (recessive) g.76890889G>A - c.2476G>A p.Ala826Thr - MYO7A_000013 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC02729 PubMed: Khateb 2020 Two affected sisters F - - Sephardic Jewish - - - - 1 LOVD
?/. - c.2476G>A r.(?) p.(Ala826Thr) - Unknown - VUS g.76890889G>A - MYO7A(NM_000260.3):c.2476G>A (p.A826T) - MYO7A_000013 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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