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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 70 c.15053-26_15298-708del r.? p.(Leu5019Valfs*77) - Parent #2 - pathogenic g.215803086_215808072del g.215629744_215634730del - - USH2A_000800 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. - c.15053-26_15298-708del r.spl p.(Leu5019Valfs*77) - Parent #2 - pathogenic g.215803086_215808072del g.215629744_215634730del USH2A exon 70 deleted c.15053-26_15298-708del, p.(Leu5019Valfs*77) - USH2A_000800 - PubMed: Steele-Stallard 2013 - - Germline yes - - - - DNA, RNA MLPA, arrayCGH, PCR, RT-PCR, SEQ - RNA isolated from nasal epithelial cells retinal disease 657_II:1 PubMed: Steele-Stallard 2013 proband of family 657_II:1 M - United Kingdom (Great Britain) white - - - - 1 LOVD
+/. - c.15053-26_15298-708del r.spl p.(Leu5019Valfs*77) - Parent #2 - pathogenic g.215803086_215808072del g.215629744_215634730del USH2A exon 70 deleted c.15053-26_15298-708del, p.(Leu5019Valfs*77) - USH2A_000800 - PubMed: Steele-Stallard 2013 - - Germline yes - - - - DNA SEQ - - retinal disease 657_II:2 PubMed: Steele-Stallard 2013 sister of proband, family 657_II:2 F - United Kingdom (Great Britain) white - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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