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     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Owner     
+/. 45i_47i c.9055+100_9371+5544dup r.(9056_9371del) p.? - Parent #2 - pathogenic g.216005789_216019066dup g.215832447_215845724dup - - USH2A_001087 Tandem duplication of exons 46 and 47 - - - Germline yes - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) USH IRD4.0_#16 Manuscript under review (González-del Pozo et al., 2018) - ? ? Spain - - - - - 1 María González-del Pozo
+?/. - c.9055+100_9371+5544dup r.(?) p.(?) - Paternal (confirmed) - likely pathogenic g.216005789_216019066dup g.215832447_215845724dup M21: Duplication Ex 46-47 c.9055 + 100_9371 + 5544dup; p.? - USH2A_001087 - PubMed: Gonzalez del Pozo 2018 - - Germline yes - - - - DNA SEQ-NG blood solved retinal disease P (II:9) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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