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.

11 entries on 1 page. Showing entries 1 - 11.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 35 c.4838del r.(?) p.(Asp1613Valfs*32) SH3 (1603-1672) Unknown - pathogenic g.76910849del g.77199804del - - MYO7A_000236 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - - +BstEII;+BspMI;+BfuAI; - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 35 c.4838del r.(?) p.(Asp1613Valfs*32) SH3 (1603-1672) Paternal (inferred) - pathogenic g.76910849del g.77199804del 4838delA - MYO7A_000236 Homozygous PubMed: Riazuddin 2008 - - Germline - - +BstEII;+BspMI;+BfuAI; - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/+ 35 c.4838del r.(?) p.(Asp1613Valfs*32) SH3 (1603-1672) Maternal (inferred) - pathogenic g.76910849del g.77199804del 4838delA - MYO7A_000236 Homozygous PubMed: Riazuddin 2008 - - Germline - - +BstEII;+BspMI;+BfuAI; - - DNA SEQ - - USH1B ? PubMed: Riazuddin 2008 Proband - - Pakistan - - - - - 1 Anne-Françoise Roux
+/. - c.4838del r.(?) p.(Asp1613Valfs*32) - Unknown - pathogenic (recessive) g.76910849del - 11:76910848GA>G ENST00000409709.3:c.4838delA (Asp1613ValfsTer32) - MYO7A_000236 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001031 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Asia-South - - - - 1 LOVD
+/. - c.4838del r.(?) p.(Asp1613Valfs*32) - Unknown - pathogenic g.76910849del g.77199804del MYO7A c.4838delA, p.Asp1613ValfsTer32 - MYO7A_000236 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001031 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+/. - c.4838del r.(?) p.(Asp1613ValfsTer32) - Both (homozygous) - pathogenic (recessive) g.76910849del g.77199804del 4838delA - MYO7A_000236 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4182 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.4838del r.(?) p.(Asp1613ValfsTer32) - Both (homozygous) - pathogenic (recessive) g.76910849del g.77199804del 4838delA - MYO7A_000236 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4513 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.4838del r.(?) p.(Asp1613ValfsTer32) - Both (homozygous) - pathogenic (recessive) g.76910849del g.77199804del 4838delA - MYO7A_000236 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4694 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.4838del r.(?) p.(Asp1613ValfsTer32) - Parent #2 - pathogenic (recessive) g.76910849del g.77199804del 4838delA - MYO7A_000236 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4190 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.4838del r.(?) p.(Asp1613ValfsTer32) - Parent #2 - pathogenic (recessive) g.76910849del g.77199804del 4838delA - MYO7A_000236 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4281 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
+/. - c.4838del r.(?) p.(Asp1613ValfsTer32) - Parent #2 - pathogenic (recessive) g.76910849del g.77199804del 4838delA - MYO7A_000236 - PubMed: Richard 2019 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL DEM4692 PubMed: Richard 2019 - - yes Pakistan - - - - - 1 Johan den Dunnen
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