Full data view for gene USH2A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_206933.2 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)     

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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.(-205+1_-204-1)_(485+1_486-1)del r.spl p.(?) - Maternal (confirmed) - VUS g.? g.? USH2A nucleotide 1, protein 1:exon 2 del, p.? nucleotide 2, protein 2:c.6289_6302del, p.Ile2097* - USH2A_000391 heterozygous, ACMG unclassified - no access to supplementary table 2 PubMed: Hull 2020 - - Germline ? - - - - DNA ? blood NGS gene panel investigation in 60 families, Sanger sequencing in 27 families, and Asper microarray in 25 families retinal disease 68 PubMed: Hull 2020 - ? - New Zealand white - - - - 1 LOVD
+/+ 68 c.14879_14880delins45 r.(?) p.(Gln4960Profs*40) Fibronectin type-III 35 (4928-5014) Parent #2 - pathogenic g.? - - - USH2A_000391 Heterozygous PubMed: Rivolta 2000 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Rivolta 2000 Proband - Genotype deduced from Sandberg et al., 2008 - - United States - - - - - 1 Anne-Françoise Roux
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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