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     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

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VIP     

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Owner     
+/+ 14 c.1563del r.(?) p.(Asp521Glufs*8) Motor domain (1-729) Unknown - pathogenic g.76873907del g.77162861del - - MYO7A_000194 Heterozygous PubMed: Le Quesne Stabej 2012 - - Germline - 0/96 controls -MslI - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 14 c.1563del r.(?) p.(Asp521Glufs*8) Motor domain (1-729) Parent #1 - pathogenic g.76873907del g.77162861del 1563delC - MYO7A_000194 Heterozygous PubMed: Liu 1997(2) - - Germline - 0/90 controls -MslI - - DNA SEQ - - USH1B ? PubMed: Liu 1997(2) Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
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