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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VIP     

Data_av     

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Owner     
+/? 2 c.1223C>T r.(?) p.(Ala408Val) N-terminal domain (1-1223) Paternal (confirmed) - pathogenic g.18023337C>T g.18120023C>T - - MYO15A_000072 heterozygous, {MSV3dQ9UKN7:p.Ala408Val} - - - Germline - - - - - DNA SEQ-NG-S - - deafness - - proband M - Israel Palestinian Arab - - - - 1 Daphne Karfunkel
+?/? 2 c.1223C>T r.(?) p.(Ala408Val) N-terminal domain (1-1223) Maternal (confirmed) ACMG VUS g.18023337C>T g.18120023C>T - - MYO15A_000072 heterozygous, {MSV3dQ9UKN7:p.Ala408Val} PubMed: Brownstein et al., 2014 - rs191710555 Germline - 0/200 controls - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein et al., 2014 proband F - Palestine - - - - - 1 Anne-Françoise Roux
+?/? 2 c.1223C>T r.(?) p.(Ala408Val) N-terminal domain (1-1223) Maternal (confirmed) ACMG VUS g.18023337C>T g.18120023C>T - - MYO15A_000072 heterozygous, {MSV3dQ9UKN7:p.Ala408Val} PubMed: Brownstein et al., 2014 - rs191710555 Germline - 0/200 controls - - - DNA SEQ - - DFNB - PubMed: Brownstein et al., 2014 relative M - Palestine - - - - - 1 Anne-Françoise Roux
-?/. - c.1223C>T r.(?) p.(Ala408Val) - Unknown - likely benign g.18023337C>T - - - MYO15A_000072 - - - rs191710555 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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