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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/+ 31 c.4065del r.(?) p.(His1355Glnfs*44) FERM 1 (1258-1602) Parent #1 - pathogenic g.76903236del g.77192191del 4065delC - MYO7A_000219 Heterozygous PubMed: Jacobson 2009 - rs111033202 Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2009 Proband F - - - - - - - 1 William J. Kimberling
+?/. - c.4065del r.(?) p.(His1355Glnfs*44) - Parent #1 - likely pathogenic g.76903236del g.77192191del - - MYO7A_000219 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs111033202 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+?/. - c.4065del r.(?) p.(His1355Glnfs*44) - Parent #1 - likely pathogenic (recessive) g.76903236del g.77192191del - - MYO7A_000219 - PubMed: Eandi 2017 - - Germline yes - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam5PatTO6 PubMed: Eandi 2017 - M - Italy - - - - - 1 LOVD
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