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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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VIP     

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Panel size     

Owner     
+/+ 23 c.4821G>A r.(?) p.(Trp1607*) Laminin G-like 1 (1517-1709) Unknown - pathogenic g.216262419C>T g.216089077C>T - - USH2A_000573 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 1/864 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.4821G>A r.(?) p.(Trp1607*) - Unknown - likely pathogenic g.216262419C>T g.216089077C>T c.1859G>T p.(Cys620Phe), c.4821G>A p.(Trp1607*) - USH2A_000573 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 024 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+?/. - c.4821G>A r.(?) p.(Trp1607*) - Parent #1 - likely pathogenic g.216262419C>T g.216089077C>T USH2A c.4821G>A - USH2A_000573 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 2 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.4821G>A r.(?) p.(Trp1607Ter) - Unknown ACMG likely pathogenic g.216262419C>T g.216089077C>T - - USH2A_000573 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Toms, M. et al., 2020 - rs745350407 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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