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.

4 entries on 1 page. Showing entries 1 - 4.
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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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Technique     

Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Panel size     

Owner     
+?/? 34 c.4450C>T r.(?) p.(Leu1484Phe) FERM 1 (1258-1602) Parent #2 ACMG VUS g.76909548C>T g.77198503C>T - - MYO7A_000182 Heterozygous PubMed: Jaijo 2006; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2006 Proband M - Spain - - - - - 1 Jose Maria Millan
?/. - c.4450C>T r.(?) p.(Leu1484Phe) - Unknown - VUS g.76909548C>T g.77198503C>T MYO7A(NM_000260.3):c.4450C>T (p.(Leu1484Phe)) - MYO7A_000182 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 34 c.4450C>T r.(?) p.(Leu1484Phe) - Parent #2 - pathogenic g.76909548C>T - c.4450C>T - MYO7A_000182 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. - c.4450C>T r.(?) p.(Leu1484Phe) - Unknown - pathogenic g.76909548C>T - MYO7A(NM_000260.3):c.4450C>T (p.(Leu1484Phe)) - MYO7A_000182 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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