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     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
+?/? 5 c.401T>A r.(?) p.(Ile134Asn) Motor domain (1-729) Unknown ACMG VUS g.76867068T>A g.77156022T>A - - MYO7A_000222 Heterozygous PubMed: Bharadwaj 2000; USMA-USMA missense analysis USMA-missense variant in MSV3d - rs111033181 Germline - 0/172 controls - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bharadwaj 2000 Proband - - Ireland - - - - - 1 Anne-Françoise Roux
+?/. - c.401T>A r.(?) p.(Ile134Asn) - Parent #1 - likely pathogenic g.76867068T>A g.77156022T>A - - MYO7A_000222 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs111033181 Germline - 1/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+?/. 5 c.401T>A r.(?) p.(Ile134Asn) - Unknown - likely pathogenic g.76867068T>A - c.401T>A,p.I134N - MYO7A_000222 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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