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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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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ClinVar ID     

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VIP     

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Disease     

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?/. - c.687C>T r.(?) p.(Gly229=) - Unknown - VUS g.76868002C>T g.77156956C>T MYO7A(NM_000260.3):c.687C>T (p.G229=) - MYO7A_000490 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 7 c.687C>T r.(?) p.(?) Motor domain (1-729) Unknown ACMG VUS g.76868002C>T g.77156956C>T - - MYO7A_000490 Heterozygous PubMed: Besnard, Garcia-Garcia 2014 - - Germline - - -BstUI - - DNA SEQ, SEQ-NG-S - - DFN ? PubMed: Besnard, Garcia-Garcia 2014 Proband M - - - - - - - 1 Anne-Françoise Roux
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