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     
+/+ 42i c.5856+1G>A r.(?) p.(?) - Parent #2 - pathogenic g.76918448G>A g.77207403G>A - - MYO7A_000091 Heterozygous PubMed: Roux 2011 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. - c.5856+1G>A r.spl p.? - Parent #2 ACMG pathogenic g.76918448G>A g.77207403G>A NM_001127180.1:c.5742+1G>A - MYO7A_000091 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ, SEQ-NG - - HL 19147 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
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