Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 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     

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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.1605C>T r.(?) p.(Asn535=) - Unknown - likely benign g.76873949C>T g.77162903C>T MYO7A(NM_000260.3):c.1605C>T (p.N535=) - MYO7A_000262 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1605C>T r.(?) p.(Asn535=) - Unknown - likely benign g.76873949C>T g.77162903C>T MYO7A(NM_000260.3):c.1605C>T (p.N535=) - MYO7A_000262 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 14 c.1605C>T r.(?) p.(=) Motor domain (1-729) Unknown - benign g.76873949C>T g.77162903C>T - - MYO7A_000262 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012 - rs111033228 Germline - 2/864 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 14 c.1605C>T r.(?) p.(=) Motor domain (1-729) Parent #1 - benign g.76873949C>T g.77162903C>T - - MYO7A_000262 Heterozygous PubMed: Roux 2011 - rs111033228 Germline - - none - - DNA SEQ - - DFNB ? PubMed: Roux 2011 Proband M - France - - - - - 1 Anne-Françoise Roux
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