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     
+/+ 34 c.4513G>T r.(?) p.(Glu1505*) - Parent #2 ACMG pathogenic (recessive) g.76909611G>T - - - MYO7A_000957 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing USH1 Pat7 PubMed: Bahena 2021 - F no Iran - - - - - 1 Barbara Vona
+/. 34 c.4513G>T r.(?) p.(Glu1505*) - Both (homozygous) - pathogenic (recessive) g.76909611G>T - c.4513G>T(p.Glu1505Ter) - MYO7A_000957 - PubMed: Kooshavar 2018 - - Germline yes - - - - DNA SEQ-NG, SEQ blood - retinal disease V:3 PubMed: Kooshavar 2018 - M yes Iran iranian - - - - 1 LOVD
+/. 34 c.4513G>T r.(?) p.(Glu1505*) - Both (homozygous) - pathogenic (recessive) g.76909611G>T - c.4513G>T(p.Glu1505Ter) - MYO7A_000957 - PubMed: Kooshavar 2018 - - Germline yes - - - - DNA SEQ blood - retinal disease V:8 PubMed: Kooshavar 2018 cousin of V:3 M yes Iran iranian - - - - 1 LOVD
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