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     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+/. 36 c.5069_5070insC r.(?) p.(Gln1690Hisfs*31) - Both (homozygous) - pathogenic g.76913370insC - - - MYO7A_000785 Variant Error [ESYNTAX]: This genomic variant has an error (insertion length must be 1). Please fix this entry and then remove this message. Sharon, submitted - - Germline - - - - - DNA SEQ - - USH1 - Sharon, submitted - F yes Israel Arab-Muslim - - - - 3 Dror Sharon
+/. - c.5069_5070insC r.(?) p.(Gln1690Hisfs*31) - Unknown ACMG pathogenic g.76913370_76913371insC - - - MYO7A_000785 - PubMed: Sharon 2019 - - Germline - 1/2420 IRD families - - - DNA SEQ - - retinal disease - PubMed: Sharon 2019 1 IRD family - - Israel - - - - - 1 Global Variome, with Curator vacancy
?/. 37 c.5069_5070insC r.(?) p.(Gln1690Hisfs*31) - Unknown - VUS g.76913370_76913371insC - c.5069_5070insC - MYO7A_000785 - PubMed: Khalaileh-2018 - - Unknown - - - - - DNA arraySNP, SEQ-NG blood WES retinal disease - PubMed: Khalaileh-2018 - - yes - Arab Muslim - - - - 1 LOVD
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