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.

2 entries on 1 page. Showing entries 1 - 2.
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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     

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Consanguinity     

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VIP     

Data_av     

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Panel size     

Owner     
+/+ 46 c.6321G>A r.(?) p.(Trp2107*) FERM 2 (1902-2205) Parent #2 - pathogenic g.76922949G>A g.77211904G>A - - MYO7A_000512 Heterozygous; possible pathogenic PubMed: Yoshimura 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Yoshimura 2014 Proband - - Japan - - - - - 1 Anne-Françoise Roux
+/+ 46 c.6321G>A r.(?) p.(Trp2107*) FERM2 (1902-2205) Parent #2 - pathogenic g.76922949G>A g.77211904G>A - - MYO7A_000512 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Spain - - - - - 1 Crystel Bonnet
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