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.

40 entries on 1 page. Showing entries 1 - 40.
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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     

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Owner     
?/. - c.2283-1G>T r.spl? p.? - Unknown - VUS g.76890090G>T g.77179044G>T - - MYO7A_000086 - PubMed: Sommen 2016, Journal: Sommen 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-I - - DFNB;ARNSHL - PubMed: Sommen 2016, Journal: Sommen 2016 - - - - - - - - - 1 Manou Sommen
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (confirmed) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Bonnet 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1 - PubMed: Bonnet 2011 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (confirmed) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Bonnet 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1 - PubMed: Bonnet 2011 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Parent #1 - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Heterozygous PubMed: Roux 2006 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Algeria - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Unknown - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Heterozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.2283_2367del p.Ser762Cysfs*61 IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous; E20 skipping (Jaijo , 2010) PubMed: Jaijo 2007 - - Germline - 0/100 controls +FatI;+NlaIII;+CviAII; - - DNA minigene, SEQ - - USH1B ? PubMed: Jaijo 2007 Proband M - Morocco - - - - - 1 Jose Maria Millan
+/+ 19i c.2283-1G>T r.2283_2367del p.Ser762Cysfs*61 IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous; E20 skipping (Jaijo , 2010) PubMed: Jaijo 2007 - - Germline - 0/100 controls +FatI;+NlaIII;+CviAII; - - DNA minigene, SEQ - - USH1B ? PubMed: Jaijo 2007 Proband M - Morocco - - - - - 1 Jose Maria Millan
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
-/- 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Algeria - - - - - 1 Anne-Françoise Roux
-/- 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - Algeria - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Roux 2011 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Unknown - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Heterozygous PubMed: Besnard, Garcia-Garcia 2014 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ, SEQ-NG-S - - ? ? PubMed: Besnard, Garcia-Garcia 2014 Proband M - Morocco - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Parent #1 - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Heterozygous PubMed: Aparisi 2014 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (confirmed) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (confirmed) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Parent #1 - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - Spain - - - - - 1 Crystel Bonnet
+/? 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (confirmed) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Heterozygous PubMed: Abdi 2016 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband M - Algeria - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Abdi 2016 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband F - Algeria - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Abdi 2016 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband F - Algeria - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Paternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Abdi 2016 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband M - Algeria - - - - - 1 Crystel Bonnet
+/+ 19i c.2283-1G>T r.(2283_2367del) p.(Ser762Cysfs*61) IQ 1 (745-765) Maternal (inferred) - pathogenic g.76890090G>T g.77179044G>T - - MYO7A_000086 Homozygous PubMed: Abdi 2016 - - Germline - - +FatI;+NlaIII;+CviAII; - - DNA SEQ - - USH1B ? PubMed: Abdi 2016 Proband M - Algeria - - - - - 1 Crystel Bonnet
+?/. - c.2283-1G>T r.spl? p.? - Unknown - likely pathogenic g.76890090G>T g.77179044G>T MYO7A(NM_000260.3):c.2283-1G>T, MYO7A(NM_000260.4):c.2283-1G>T - MYO7A_000086 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.2283-1G>T r.spl? p.? - Unknown - pathogenic g.76890090G>T g.77179044G>T MYO7A(NM_000260.3):c.2283-1G>T, MYO7A(NM_000260.4):c.2283-1G>T - MYO7A_000086 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.2283-1G>T r.(?) p.? - Both (homozygous) - pathogenic (recessive) g.76890090G>T g.77179044G>T - - MYO7A_000086 - PubMed: Riahi 2015 - - Germline yes - - - - DNA SEQ-NG - WES deafness FamDF11 PubMed: Riahi 2015 6-generation family, 4 affected (3F, M), unaffected heterozygous carrier parents/relatives F;M yes Tunisia - - - - - 4 LOVD
+/. - c.2283-1G>T r.(?) p.(Ser762CysfsTer61) - Unknown ACMG pathogenic g.76890090G>T - - - MYO7A_000086 - PubMed: Mansard et al, 2021 - rs397516295 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.2283-1G>T r.(?) p.(Ser762CysfsTer61) - Both (homozygous) ACMG pathogenic g.76890090G>T - - - MYO7A_000086 - PubMed: Mansard et al, 2021 - rs397516295 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.2283-1G>T r.(?) p.(Ser762CysfsTer61) - Both (homozygous) ACMG pathogenic g.76890090G>T - - - MYO7A_000086 - PubMed: Mansard et al, 2021 - rs397516295 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.2283-1G>T r.(?) p.(Ser762CysfsTer61) - Both (homozygous) ACMG pathogenic g.76890090G>T - - - MYO7A_000086 - PubMed: Mansard et al, 2021 - rs397516295 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.2283-1G>T r.(?) p.(Ser762CysfsTer61) - Maternal (confirmed) ACMG pathogenic g.76890090G>T - - - MYO7A_000086 - PubMed: Mansard et al, 2021 - rs397516295 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 19i c.2283-1G>T r.spl? p.? - Both (homozygous) - likely pathogenic (recessive) g.76890090G>T - c.2283-1G>T - MYO7A_000086 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC06518 PubMed: Khateb 2020 affected brother F yes - Tunisian - - - - 1 LOVD
+?/. 19i c.2283-1G>T r.spl? p.? - Both (homozygous) - likely pathogenic (recessive) g.76890090G>T - c.2283-1G>T - MYO7A_000086 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC3672 PubMed: Khateb 2020 one affected sister M - - North African - - - - 1 LOVD
+?/. 19i c.2283-1G>T r.spl? p.? - Both (homozygous) - likely pathogenic (recessive) g.76890090G>T - c.2283-1G>T - MYO7A_000086 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08844 PubMed: Khateb 2020 one affected brother F - - Algerian - - - - 1 LOVD
+/. 19i c.2283-1G>T r.spl? p.? - Both (homozygous) - pathogenic g.76890090G>T - c.2283-1G>T - MYO7A_000086 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. - c.2283-1G>T r.spl? p.? - Unknown - pathogenic g.76890090G>T - MYO7A(NM_000260.3):c.2283-1G>T, MYO7A(NM_000260.4):c.2283-1G>T - MYO7A_000086 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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