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     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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VIP     

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Disease     

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Owner     
+/? 6 c.487G>C r.(?) p.(Gly163Arg) Motor domain (1-729);ATP binding site (158-165) Parent #1 ACMG likely pathogenic g.76867722G>C g.77156676G>C - - MYO7A_000073 Heterozygous PubMed: Roux 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/664 controls - - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Algeria - - - - - 1 Anne-Françoise Roux
+/? 6 c.487G>C r.(?) p.(Gly163Arg) Motor domain (1-729);ATP binding site (158-165) Parent #1 ACMG likely pathogenic g.76867722G>C g.77156676G>C - - MYO7A_000073 Heterozygous PubMed: Jacobson 2008; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jacobson 2008 Proband M - - - - - - - 1 Anne-Françoise Roux
+?/. 6 c.487G>C r.(?) p.(Gly163Arg) - Unknown - likely pathogenic g.76867722G>C - p.G163R - MYO7A_000073 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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