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.

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     
+/+ 28 c.3596dup r.(?) p.(Cys1201Leufs*28) MyTH4 1 (1017-1253) Parent #2 - pathogenic g.76900481dup g.77189436dup - - MYO7A_000199 Heterozygous PubMed: Liu 1997 - - Germline - - - - - DNA SEQ - - DFNB ? PubMed: Liu 1997 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 28 c.3596dup r.(?) p.(Cys1201Leufs*28) MyTH4 1 (1017-1253) Parent #2 - pathogenic g.76900481dup g.77189436dup - - MYO7A_000199 Heterozygous PubMed: Liu 1997 - - Germline - - - - - DNA SEQ - - DFNB ? PubMed: Liu 1997 Relative F - China - - - - - 1 Anne-Françoise Roux
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