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.

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     
+/+ 29i c.5857+2T>C r.spl p.? - Parent #2 - pathogenic g.216246229A>G g.216072887A>G - - USH2A_000389 Heterozygous PubMed: Sandberg 2008 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Sandberg 2008 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 29i c.5857+2T>C r.spl p.? - Unknown - pathogenic g.216246229A>G g.216072887A>G - - USH2A_000389 Heterozygous PubMed: McGee 2010 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: McGee 2010 No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
+?/. - c.5857+2T>C r.spl p.? - Parent #2 - likely pathogenic g.216246229A>G g.216072887A>G IVS29+2T>C - USH2A_000389 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 582 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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