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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/? 26 c.2777T>A r.(?) p.(Leu926Gln) - Both (homozygous) ACMG VUS g.76599892T>A g.75890175T>A - - MYO6_000011 homozygous, {MSV3dQ9UM54:p.(Leu926Gln)} PubMed: Brownstein et al., 2014 - - Germline - 0/200 controls - - - DNA SEQ, SEQ-NG-S - - DFNB - PubMed: Brownstein et al., 2014 proband M - Palestine - - - - - 1 Anne-Françoise Roux
+?/? 26 c.2777T>A r.(?) p.(Leu926Gln) - Both (homozygous) ACMG VUS g.76599892T>A g.75890175T>A - - MYO6_000011 homozygous, {MSV3dQ9UM54:p.(Leu926Gln)} PubMed: Brownstein et al., 2014 - - Germline - 0/200 controls - - - DNA SEQ - - DFNB - PubMed: Brownstein et al., 2014 relative F - Palestine - - - - - 1 Anne-Françoise Roux
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