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.

3 entries on 1 page. Showing entries 1 - 3.
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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     

Country     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. 63 c.12332C>T r.(?) p.(Ser4111Phe) - Unknown - likely pathogenic g.215848921G>A g.215675579G>A USH2A Ex.5 c.841A>C p.(Thr281Pro), Ex.63 c.12332C>T p.(Ser4111Phe) - USH2A_002207 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-3008 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
?/. - c.12332C>T r.(?) p.(Ser4111Phe) - Unknown - VUS g.215848921G>A g.215675579G>A USH2A c.12332C>T, p.Ser4111Phe - USH2A_002207 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 121-1052 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
?/. - c.12332C>T r.(?) p.(Ser4111Phe) - Unknown - VUS g.215848921G>A - USH2A(NM_206933.2):c.12332C>T (p.S4111F) - USH2A_002207 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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