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.

6 entries on 1 page. Showing entries 1 - 6.
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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     
+?/. 29 c.3892G>A r.(?) p.(Gly1298Arg) - Both (homozygous) - likely pathogenic g.76901883G>A g.77190838G>A - - MYO7A_000784 - Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - M yes Israel Arab-Muslim - - - - 3 Dror Sharon
+?/. - c.3892G>A r.(?) p.(Gly1298Arg) - Unknown ACMG likely pathogenic g.76901883G>A - - - MYO7A_000784 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
+/. 30 c.3892G>A r.(?) p.(Gly1298Arg) - Unknown - pathogenic g.76901883G>A - c.3892G>A - MYO7A_000784 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA SEQ-NG blood WES retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
+/. 30 c.3892G>A r.(?) p.(Gly1298Arg) - Unknown - pathogenic g.76901883G>A - c.3892G>A - MYO7A_000784 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA arraySNP, SEQ-NG blood WES retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
+/. 30 c.3892G>A r.(?) p.(Gly1298Arg) - Parent #2 - pathogenic (recessive) g.76901883G>A - c.3892G>A - MYO7A_000784 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease 1597918 PubMed: Khateb 2020 Simplex case F - - Austrian - - - - 1 LOVD
+/. 30 c.3892G>A r.(?) p.(Gly1298Arg) - Parent #1 - pathogenic (recessive) g.76901883G>A - c.3892G>A p.Gly1298Arg - MYO7A_000784 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08509 PubMed: Khateb 2020 Simplex case F - - - - - - - 1 LOVD
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