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)     

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+?/? 23 c.2837T>G r.(?) p.(Met946Arg) - Maternal (confirmed) ACMG VUS g.76892568T>G g.77181522T>G - - MYO7A_000515 Heterozygous; causative PubMed: Rong 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/200 controls - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Rong 2014 Proband - variants found in samples of two affected brothers. They carry the same causative mutations in MYO7A, but other variants cannot be discriminated from the publication. M - China - - - - - 1 Anne-Françoise Roux
+?/? 23 c.2837T>G r.(?) p.(Met946Arg) - Parent #2 ACMG VUS g.76892568T>G g.77181522T>G - - MYO7A_000515 Heterozygous; mutation PubMed: Jiang 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+/. - c.2837T>G r.(?) p.(Met946Arg) - Both (homozygous) ACMG pathogenic g.76892568T>G g.77181522T>G - - MYO7A_000515 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ-NG - - HL 73013 PubMed: Sun 2018 sporadic case - yes China - - - - - 1 LOVD
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