Full data view for gene MYO15A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_016239.3 transcript reference sequence.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Owner     
+?/. - c.3524dup r.(?) p.(Ser1176Valfs*14) - Paternal (confirmed) ACMG pathogenic (recessive) g.18025638dup g.18122324dup 3524_3525insA - MYO15A_000377 in compund heterozygosis with c.1615C>T PubMed: Batissoco 2021 ClinVar-SCV001792220 - Germline yes - - - - DNA SEQ-NG-I - - HL M1 PubMed: Batissoco 2021 - F no Brazil - - - - - 1 Karina Lezirovitz Mandelbaum
+/. - c.3524dup r,(?) p.(Ser1176ValfsTer14) - Parent #1 - pathogenic (recessive) g.18025638dup g.18122324dup 3524dupA - MYO15A_000377 combination of alleles not reported PubMed: Wu 2019 - - Germline - 9/1291 cases hearing loss - - - DNA SEQ, SEQ-NG - 213-gene panel HL - PubMed: Wu 2019 analysis 1291 cases hearing loss - - Taiwan - - - - - 9 Johan den Dunnen
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