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     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.6634G>A r.(?) p.(Glu2212Lys) - Unknown - likely pathogenic g.18051467G>A - - - MYO15A_000409 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.6634G>A r.(?) p.(Glu2212Lys) - Parent #2 ACMG pathogenic (recessive) g.18051467G>A g.18148153G>A - - MYO15A_000409 - PubMed: Wonkam 2022 - rs371352836 Germline yes - - - - DNA SEQ, SEQ-NG-I Blood WES DFNB3 Fam34 PubMed: Wonkam 2022 3-generation family, 2 affected brothers M no Ghana Africa - - - - 2 Yacouba Dia
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