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)     

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     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 4 c.781_784+1375del r.spl? p.? - Maternal (inferred) - pathogenic g.216536924_216538302del g.216363582_216364960del - - USH2A_000799 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.781_784+1375del r.spl p.? - Parent #1 - likely pathogenic g.216536924_216538302del g.216363582_216364960del 781_c784+1375del1379ttaAATG… - USH2A_000799 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 580 PubMed: Stone 2017 1 affected M - (United States) - - - - - 1 LOVD
+/. - c.781_784+1375del r.spl p.? - Maternal (inferred) - pathogenic g.216536924_216538302del g.216363582_216364960del USH2A exon 4 deleted c.781_784+1375del, p.? - USH2A_000799 - PubMed: Steele-Stallard 2013 - - Germline yes - - - - DNA MLPA, arrayCGH, PCR, SEQ - - retinal disease 309_II:1 PubMed: Steele-Stallard 2013 proband of family 309_II:1 M - United Kingdom (Great Britain) white - - - - 1 LOVD
+/. 4_4i c.781_784+1375del r.? p.? - Parent #1 ACMG pathogenic (recessive) g.216536920_216538298del g.216363578_216364956del - - USH2A_000799 - PubMed: de Bruijn 2023 - - Germline - - - - - DNA SEQ, SEQ-NG - - USH 071975 PubMed: de Bruijn 2023 - - - - - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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