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     
+/+ 31 c.4036_4038del r.(?) p.(Phe1346del) FERM 1 (1258-1602) Parent #1 - pathogenic g.76903207_76903209del g.77192162_77192164del 4036_4038delTTC - MYO7A_000230 Heterozygous PubMed: Bharadwaj 2000 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Bharadwaj 2000 Proband - - France - - - - - 1 Anne-Françoise Roux
+/? 31 c.4036_4038del r.(?) p.(Phe1346del) FERM 1 (1258-1602) Unknown - pathogenic g.76903207_76903209del g.77192162_77192164del 4036_4038delTTC - MYO7A_000230 Heterozygous PubMed: Roux 2011 - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 31 c.4036_4038del r.(?) p.(Phe1346del) FERM1 (1258-1602) Unknown - pathogenic g.76903207_76903209del g.77192162_77192164del 4036_4038delTTC - MYO7A_000230 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
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