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)     

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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+?/. - c.10182+1G>A r.spl p.? - Parent #2 - likely pathogenic g.215963400C>T g.215790058C>T - - USH2A_001912 - PubMed: Soens 2017 - - Germline - - - - - DNA SEQ - - retinal disease SRF_1694 PubMed: Soens 2017 possible duplicate - - - - - - - - 1 LOVD
+/. 51i c.10182+1G>A r.spl p.(?) - Parent #1 ACMG pathogenic g.215963400C>T g.215790058C>T USH2A c.10182+1G>A - USH2A_001912 single heterozygous variant in a recessive disesase, no second allele PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf58 PubMed: Zhu 2021 family 257, patient USHsrf58 F - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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