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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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VIP     

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Panel size     

Owner     
+/. 17 c.3635C>T r.(?) p.(Pro1212Leu) - Parent #2 - pathogenic (recessive) g.216373145G>A g.216199803G>A - - USH2A_000490 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-14 (D54) PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - F no Denmark - - - - - 1 Anne-Françoise Roux
+?/. - c.3635C>T r.(?) p.(Pro1212Leu) - Unknown ACMG likely pathogenic g.216373145G>A g.216199803G>A USH2A c.3635C>T(;)4576G>A, V2: c.3635C>T, (p.Pro1212Leu) - USH2A_000490 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F123 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+?/. - c.3635C>T r.(?) p.(Pro1212Leu) - Unknown - likely pathogenic g.216373145G>A g.216199803G>A USH2A c.3635C>T(;)4576G>A; p.(Pro1212Leu) - USH2A_000490 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0; GnomAD_exome_East: 0; GnomAD_All: 0 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F123 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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