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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ClinVar ID     

dbSNP ID     

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Owner     
+/+ 7 c.655_660del r.(?) p.(Ile219_His220del) Motor domain (1-729) Paternal (inferred) ACMG VUS g.76867970_76867975del g.77156924_77156929del - - MYO7A_000174 Homozygous PubMed: Jaijo 2007 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2007 Proband M - Morocco - - - - - 1 Jose Maria Millan
+/+ 7 c.655_660del r.(?) p.(Ile219_His220del) Motor domain (1-729) Maternal (inferred) ACMG VUS g.76867970_76867975del g.77156924_77156929del - - MYO7A_000174 Homozygous PubMed: Jaijo 2007 - - Germline - 0/100 controls - - - DNA SEQ - - USH1B ? PubMed: Jaijo 2007 Proband M - Morocco - - - - - 1 Jose Maria Millan
+/. - c.655_660del r.(?) p.(Ile219_His220del) - Parent #1 - pathogenic (recessive) g.76867970_76867975del g.77156924_77156929del - - MYO7A_000174 - PubMed: Fuster-Garcia 2018 - - Germline - - - - - DNA arraySEQ - - retinal disease RP1757t PubMed: Fuster-Garcia 2018 analysis 77 USH patients - - Spain - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.655_660del r.(?) p.(Ile219_His220del) - Parent #1 - likely pathogenic g.76867970_76867975del g.77156924_77156929del MYO7A, variant 1: c.655_660del/p.I219_H220del, variant 2: c.655_660del/p.I219_H220del - MYO7A_000174 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 175 PubMed: Weisschuh 2020 Filing key number: 68, Usher syndrome type I, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. - c.655_660delATCCAC r.(?) p.(Ile219_His220del) - Paternal (confirmed) ACMG likely pathogenic g.76867970_76867975del - - - MYO7A_000174 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
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