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.

2 entries on 1 page. Showing entries 1 - 2.
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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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VIP     

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+/. 1i c.18+2T>A r.spl p.? - Unknown - pathogenic g.76841700T>A g.77130654T>A - - MYO7A_000605 - PubMed: Sommen 2016, Journal: Sommen 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-I - - DFNB;ARNSHL - PubMed: Sommen 2016, Journal: Sommen 2016 - - - - - - - - - 1 Manou Sommen
+?/. - c.18+2T>A r.spl p.(?) - Parent #1 - likely pathogenic g.76841700T>A g.77130654T>A MYO7A, variant 1: c.18+2T>A/p.?, variant 2: c.18+2T>A/p.? - MYO7A_000605 solved, homozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET4 targeted sequencing panel - see paper retinal disease 597 PubMed: Weisschuh 2020 Filing key number: 215, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
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