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.

2 entries on 1 page. Showing entries 1 - 2.
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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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 6i c.592+1G>T r.(?) p.(?) - Unknown - pathogenic g.76867828G>T g.77156782G>T - - MYO7A_000252 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -HpyAV - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 6i c.592+1G>T r.spl p.? - Parent #2 - pathogenic g.76867828G>T g.77156782G>T - - MYO7A_000252 Heterozygous PubMed: Jacobson 2008 - - Germline - - -HpyAV - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
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