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     

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AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+?/+ 12 c.1307T>C r.(?) p.(Leu436Pro) Motor domain (1-729) Parent #1 ACMG VUS g.76872125T>C g.77161079T>C - - MYO7A_000553 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. 12 c.1307T>C r.(?) p.(Leu436Pro) - Maternal (confirmed) - likely pathogenic (recessive) g.76872125T>C - c.1307T>C p.Leu436Pro - MYO7A_000553 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC00309 PubMed: Khateb 2020 Simplex case M - - - - - - - 1 LOVD
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