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.

4 entries on 1 page. Showing entries 1 - 4.
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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     
+/+ 23 c.2874_2878del r.(?) p.(Gln959Glyfs*5) - Paternal (inferred) - pathogenic g.76892605_76892609del g.77181559_77181563del 2874_2878delCCAGG - MYO7A_000063 Homozygous PubMed: Blanchet 2007 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Blanchet 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 23 c.2874_2878del r.(?) p.(Gln959Glyfs*5) - Maternal (inferred) - pathogenic g.76892605_76892609del g.77181559_77181563del 2874_2878delCCAGG - MYO7A_000063 Homozygous PubMed: Blanchet 2007 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Blanchet 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 23 c.2874_2878del r.(?) p.(Gln959Glyfs*5) - Paternal (confirmed) - pathogenic g.76892605_76892609del g.77181559_77181563del 2874_2878delCCAGG - MYO7A_000063 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
+/+ 23 c.2874_2878del r.(?) p.(Gln959Glyfs*5) - Maternal (confirmed) - pathogenic g.76892605_76892609del g.77181559_77181563del 2874_2878delCCAGG - MYO7A_000063 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
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