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     
+?/. - c.849+5G>A r.spl p.? - Parent #1 - likely pathogenic g.76868443G>A g.77157397G>A - - MYO7A_000962 - PubMed: Neuhaus 2017 - - Germline - - - - - DNA SEQ-NG - gene panel USH Pat9 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
?/. - c.849+5G>A r.spl? p.? - Unknown - VUS g.76868443G>A - - - MYO7A_000962 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.849+5G>A r.spl? p.? - Unknown ACMG likely pathogenic (recessive) g.76868443G>A g.77157397G>A - - MYO7A_000962 ACMG PP3, PM2, PP5_STRONG PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHI-3 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
+?/. - c.849+5G>A r.spl? p.? - Paternal (confirmed) ACMG likely pathogenic (recessive) g.76868443G>A g.77157397G>A - - MYO7A_000962 ACMG PP3, PM2, PP5_STRONG PubMed: Weisschuh 2024 397611 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-323 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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