Full data view for gene MYO6


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_004999.3 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     
+/+ 23i c.2417-1758T>G r.[=,2286_2287ins_2417-1876_2417-1759] p.? Motor domain (57-771) Paternal (confirmed) - pathogenic g.76593963T>G g.75884246T>G IVS23+2321T>G - MYO6_000006 - PubMed: Hilgert 2008 - - Germline - 0/278 controls - - - DNA SEQ - - DFNA1 Fam2 PubMed: Hilgert 2008 proband, 6-generation family, 17 affected (9F, 8M) F - Belgium - - - - - 17 Anne-Françoise Roux
+/+ 23i c.2417-1758T>G r.[=,2286_2287ins_2417-1876_2417-1759] p.? Motor domain (57-771) Paternal (confirmed) - pathogenic g.76593963T>G g.75884246T>G IVS23+2321T>G - MYO6_000006 - PubMed: Hilgert 2008 - - Germline - 0/278 controls - - - DNA SEQ - - DFNA1 Fam2 PubMed: Hilgert 2008 relative F - Belgium - - - - - 1 Anne-Françoise Roux
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