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.

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Disease     

ID_report     

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Owner     
-/? 2 c.1783G>A r.(?) p.(Ala595Thr) N-terminal domain (1-1223) Both (homozygous) ACMG VUS g.18023897G>A g.18120583G>A - - MYO15A_000043 homozygous, {MSV3dQ9UKN7:p.Ala595Thr} PubMed: Kalay et al., 2007 - rs2955365 Germline - - +BbsI;+MboII;-PhoI;-Sau96I;-HaeIII;-HpyAV; - - DNA SEQ - - DFNB - PubMed: Kalay et al., 2007 proband F - Turkey - - - - - 1 Anne-Françoise Roux
-/. - c.1783G>A r.(?) p.(Ala595Thr) - Unknown - benign g.18023897G>A g.18120583G>A MYO15A(NM_016239.3):c.1783G>A (p.A595T), MYO15A(NM_016239.4):c.1783G>A (p.A595T) - MYO15A_000043 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.1783G>A r.(?) p.(Ala595Thr) - Unknown - benign g.18023897G>A g.18120583G>A MYO15A(NM_016239.3):c.1783G>A (p.A595T), MYO15A(NM_016239.4):c.1783G>A (p.A595T) - MYO15A_000043 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1783G>A r.(?) p.(Ala595Thr) - Both (homozygous) - VUS g.18023897G>A - A595T - MYO15A_000043 - PubMed: Taghipour-Sheshdeh 2019, - - Germline - - - - - DNA SEQ, SEQ-NG Blood Otogenetics Deafness Panel DFNB49 FamPat22 PubMed: Taghipour-Sheshdeh 2019 5-generation family, 3 affected (F, 2M), unaffected heterozygous carrier parents/relatives M yes Iran Arab - - - - 3 Yacouba Dia
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