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     
+/. 18i c.2187+1G>T r.spl p.? - Both (homozygous) - pathogenic g.76886511G>T g.77175465G>T - - MYO7A_000782 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - M yes Israel Arab-Muslim - - - - 1 Dror Sharon
+/. - c.2187+1G>T r.spl p.? - Unknown ACMG pathogenic g.76886511G>T - - - MYO7A_000782 - PubMed: Sharon 2019 - - Germline - 2/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 2 IRD families - - Israel - - - - - 2 Global Variome, with Curator vacancy
?/. 18i c.2187+1G>T r.spl? p.? - Unknown - VUS g.76886511G>T - c.2187+1G>T - MYO7A_000782 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA arraySNP, SEQ-NG blood WES retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
?/. 18i c.2187+1G>T r.spl? p.? - Unknown - VUS g.76886511G>T - c.2187+1G>T - MYO7A_000782 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA PCR, SEQ blood - retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
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