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     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+?/? 6 c.493A>G r.(?) p.(Thr165Ala) Motor domain (1-729);ATP binding site (158-165) Parent #2 ACMG VUS g.76867728A>G g.77156682A>G - - MYO7A_000103 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/664 controls - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 6 c.493A>G r.(?) p.(Thr165Ala) Motor domain (1-729);ATP binding site (158-165) Parent #1 ACMG VUS g.76867728A>G g.77156682A>G - - MYO7A_000103 Heterozygous PubMed: Roux 2011; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/664 controls - - - DNA SEQ - - USH1B ? PubMed: Roux 2011 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/. - c.493A>G r.(?) p.(Thr165Ala) - Unknown ACMG likely pathogenic g.76867728A>G - - - MYO7A_000103 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
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