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)     

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.3665C>T r.(?) p.(Ala1222Val) - Unknown ACMG likely pathogenic g.216373115G>A g.216199773G>A USH2A c.3665C>T(;)4576G>A, V1: c.3665C>T, (p.Ala1222Val) - USH2A_002471 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F024 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+?/. - c.3665C>T r.(?) p.(Ala1222Val) - Unknown - likely pathogenic g.216373115G>A g.216199773G>A USH2A c.3665C>T(;)4576G>A; p.(Ala1222Val) - USH2A_002471 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0.001318; GnomAD_exome_East: 0.000655; GnomAD_All: 0.0000597 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F024 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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