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.

3 entries on 1 page. Showing entries 1 - 3.
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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.510G>A r.(?) p.(Leu170=) - Unknown - benign g.76867745G>A g.77156699G>A MYO7A(NM_000260.3):c.510G>A (p.L170=), MYO7A(NM_000260.4):c.510G>A (p.L170=) - MYO7A_000077 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.510G>A r.(?) p.(Leu170=) - Unknown - likely benign g.76867745G>A g.77156699G>A MYO7A(NM_000260.3):c.510G>A (p.L170=), MYO7A(NM_000260.4):c.510G>A (p.L170=) - MYO7A_000077 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 6 c.510G>A r.(?) p.(=) Motor domain (1-729) Parent #2 - benign g.76867745G>A g.77156699G>A - - MYO7A_000077 Heterozygous PubMed: Roux 2006 - rs34477144 Germline - - - - - DNA minigene, SEQ - - USH1B ? PubMed: Roux 2006 Proband M - Algeria - - - - - 1 Anne-Françoise Roux
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