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     

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DNA change (hg38)     

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Owner     
+?/+ 44 c.6025G>A r.(?) p.(Ala2009Thr) FERM2 (1902-2205) Parent #2 ACMG VUS g.76919822G>A g.77208777G>A - - MYO7A_000579 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs397516325 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+?/. 44 c.6025G>A r.(?) p.(Ala2009Thr) - Unknown - likely pathogenic g.76919822G>A - c.6025G>A,p.A2009T - MYO7A_000579 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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