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     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.9860_9873del r.(?) p.(His3287Profs*54) - Unknown - likely pathogenic (recessive) g.215972334_215972347del - 1:215972333GGCCATGGCCATCAT>G ENST00000307340.3:c.9860_9873delATGATGGCCATGGC (His3287ProfsTer54) - USH2A_001812 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G005241 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Asia-South - - - - 1 LOVD
+/. - c.9860_9873del r.(?) p.(His3287Profs*54) - Both (homozygous) - pathogenic (recessive) g.215972334_215972347del - 1:215972333GGCCATGGCCATCAT>G ENST00000307340.3:c.9860_9873delATGATGGCCATGGC (His3287ProfsTer54) - USH2A_001812 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease W000158 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Asia-South - - - - 1 LOVD
+?/. - c.9860_9873del r.(?) p.(His3287Profs*54) - Both (homozygous) - likely pathogenic g.215972335_215972348del g.215798993_215799006del USH2A c.9860_9873delATGATGGCCATGGC, p.His3287ProfsTer54 - USH2A_001812 homozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease W000158 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - 1 LOVD
+?/. - c.9860_9873del r.(?) p.(His3287Profs*54) - Parent #1 - likely pathogenic g.215972335_215972348del g.215798993_215799006del USH2A c.9860_9873del - USH2A_001812 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 50 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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