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.

6 entries on 1 page. Showing entries 1 - 6.
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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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/. - c.2809+1G>A r.spl? p.? - Unknown - pathogenic g.216419926C>T g.216246584C>T USH2A(NM_206933.4):c.2809+1G>A - USH2A_000361 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 13i c.2809+1G>A r.spl p.? - Paternal (inferred) - pathogenic g.216419926C>T g.216246584C>T - - USH2A_000361 Homozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 13i c.2809+1G>A r.spl p.? - Maternal (inferred) - pathogenic g.216419926C>T g.216246584C>T - - USH2A_000361 Homozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - - - - - - - 1 Anne-Françoise Roux
+?/. 13i c.2809+1G>A r.(?) p.(?) - Unknown - likely pathogenic g.216419926C>T g.216246584C>T USH2A Ex.13 c.2276G>T p.(Cys759Phe), IVS13 c.2809+1G>A p.(?) - USH2A_000361 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-1642 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+/. - c.2809+1G>A r.(?) p.(?) - Maternal (confirmed) ACMG pathogenic g.216419926C>T - - - USH2A_000361 - PubMed: Mansard et al, 2021 - rs759433119 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.2809+1G>A r.spl p.? - Unknown ACMG pathogenic g.216419926C>T g.216246584C>T - - USH2A_000361 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Mansard, L. et al., 2021; PubMed: Sloan-Heggen, C. M. et al., 2016 - rs759433119 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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