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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 32i c.4323+2T>C r.spl p.? - Parent #1 - pathogenic g.76905571T>C g.77194526T>C - - MYO7A_000547 Heterozygous; mutation PubMed: Jiang 2015 - rs752388932 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
?/. - c.4323+2T>C r.spl p.(?) - Unknown ACMG VUS g.76905571T>C g.77194526T>C MYO7A c.4323+2T>C, . - MYO7A_000547 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 119 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. 32i c.4323+2T>C r.spl? p.? - Both (homozygous) - likely pathogenic (recessive) g.76905571T>C - c.4323+2T>C - MYO7A_000547 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC08982 PubMed: Khateb 2020 Simplex case F yes - - - - - - 1 LOVD
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