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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
+?/? 40 c.5516T>C r.(?) p.(Leu1839Pro) MyTH4 2 (1747-1896) Parent #1 ACMG VUS g.76916542T>C g.77205497T>C - - MYO7A_000520 Heterozygous; UV3 PubMed: Aparisi 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 ? PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/. - c.5516T>C r.(?) p.(Leu1839Pro) - Parent #1 - pathogenic (recessive) g.76916542T>C g.77205497T>C - - MYO7A_000520 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1567 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+/. - c.5516T>C r.(?) p.(Leu1839Pro) - Parent #2 - pathogenic (recessive) g.76916542T>C g.77205497T>C - - MYO7A_000520 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1967 PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+/. 40 c.5516T>C r.(?) p.(Leu1839Pro) - Parent #1 - pathogenic g.76916542T>C - c.5516T>C - MYO7A_000520 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 8 LOVD
+/. 40 c.5516T>C r.(?) p.(Leu1839Pro) - Parent #2 - pathogenic g.76916542T>C - c.5516T>C - MYO7A_000520 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
+/. 40 c.5516T>C r.(?) p.(Leu1839Pro) - Parent #1 - pathogenic g.76916542T>C - c.5516T>C - MYO7A_000520 - PubMed: Galbis-Martinez-2021 - - Germline - - - - - DNA ? - - retinal disease - PubMed: Galbis-Martinez-2021 - - - - - - - - - 4 LOVD
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