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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 36 c.4919del r.(?) p.(Gly1640Alafs*5) SH3 (1603-1672) Unknown - pathogenic g.76912559del g.77201514del 4918delG - MYO7A_000351 Heterozygous PubMed: Kimberling 2010 - - Germline - - +BceAI - - DNA SEQ - - DFNB ? PubMed: Kimberling 2010 Proband - No ophtalmologic examination - - United States - - - - - 1 Anne-Françoise Roux
?/. - c.4919del r.(?) p.(Gly1640Alafs*5) - Unknown - VUS g.76912559del g.77201514del MYO7A c.4919del, p.Gly1640AlafsTer5 - MYO7A_000351 unsolved PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 121-142 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
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