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.

4 entries on 1 page. Showing entries 1 - 4.
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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     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+/. - c.14174G>A r.(?) p.(Trp4725Ter) - Unknown - pathogenic g.215824103C>T g.215650761C>T - - USH2A_001311 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.14174G>A r.(?) p.(Trp4725*) - Unknown - likely pathogenic g.215824103C>T g.215650761C>T c.14174G>A, p.Trp4725Ter - USH2A_001311 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2944_004529 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. 65 c.14174G>A r.(?) p.(Trp4725*) - Unknown - pathogenic g.215824103C>T - c.14174G>A - USH2A_001311 - PubMed: Colombo-2020 - - Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. - c.14174G>A r.(?) p.(Trp4725Ter) - Unknown ACMG pathogenic g.215824103C>T g.215650761C>T - - USH2A_001311 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2021 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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