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     
+?/. - c.285+2T>C r.spl p.? - Both (homozygous) - likely pathogenic g.76858998T>C g.77147952T>C IVS4+2T>C - MYO7A_000939 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 529 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. - c.285+2T>C r.(?) p.(?) - Unknown ACMG pathogenic g.76858998T>C - - - MYO7A_000939 - PubMed: Mansard et al, 2021 - rs782292032 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 4i c.285+2T>C r.spl? p.? - Unknown - likely pathogenic g.76858998T>C - c.285+2T>C - MYO7A_000939 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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