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     
+/. 27 c.3500T>A r.(?) p.(Leu1167His) - Paternal (inferred) - pathogenic (recessive) g.76895757T>A - c.3500T>A - MYO7A_001059 - PubMed: Bakhchane 2017 - - Unknown yes 0/100 healthy controls - - - DNA SEQ-NG, SEQ blood - retinal disease SF42.03 PubMed: Bakhchane 2017 - F - - Moroccan - - - - 1 LOVD
+/. 27 c.3500T>A r.(?) p.(Leu1167His) - Paternal (inferred) - pathogenic (recessive) g.76895757T>A - c.3500T>A - MYO7A_001059 - PubMed: Bakhchane 2017 - - Unknown yes 0/100 healthy controls - - - DNA SEQ-NG, SEQ blood - retinal disease SF42.14 PubMed: Bakhchane 2017 - M - - Moroccan - - - - 1 LOVD
+/. 27 c.3500T>A r.(?) p.(Leu1167His) - Paternal (inferred) - pathogenic (recessive) g.76895757T>A - c.3500T>A - MYO7A_001059 - PubMed: Bakhchane 2017 - - Unknown yes 0/100 healthy controls - - - DNA SEQ blood - retinal disease SF42:04,06 PubMed: Bakhchane 2017 - M;F - - Moroccan - - - - 2 LOVD
+/. 27 c.3500T>A r.(?) p.(Leu1167His) - Paternal (inferred) - pathogenic (recessive) g.76895757T>A - c.3500T>A - MYO7A_001059 - PubMed: Bakhchane 2017 - - Unknown yes 0/100 healthy controls - - - DNA SEQ blood - retinal disease SF42:12,13,14,15 PubMed: Bakhchane 2017 - M;F - - Moroccan - - - - 4 LOVD
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