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.

10 entries on 1 page. Showing entries 1 - 10.
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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     
+/+ 22-24 c.4627+25435_4987+660del r.(?) p.(?) Laminin G-like 1 (1517-1709) Maternal (confirmed) - pathogenic g.216259402_216323160del g.216086060_216149818del del22-23 - USH2A_000095 Heterozygous; nomenclature modified 12/2012 PubMed: Baux 2007 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband F - Romania - - - - - 1 Anne-Françoise Roux
+/+ 21i_24i c.4627+25435_4987+660del r.(4628_4987del) p.? Laminin G-like 1 (1517-1709) Parent #2 - pathogenic g.216259402_216323160del g.216086060_216149818del hg19:chr1:g.216259403_216323159del - USH2A_000095 Heterozygous PubMed: Dad 2015, PubMed: Dad 2016 - - Germline - - - - - DNA MLPA, SEQ - - USH2 USH2-5 (D61);USH2-5 (D61) PubMed: Dad 2015, PubMed: Dad 2016 Proband F - - - - - - - 1 Shzeena Dad
+/+ 22-24 c.4627+25435_4987+660del r.(?) p.(?) - Parent #2 - pathogenic g.216259402_216323160del g.216086060_216149818del - - USH2A_000095 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 22-24 c.4627+25435_4987+660del r.(?) p.(?) - Unknown - pathogenic g.216259402_216323160del g.216086060_216149818del - - USH2A_000095 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA PCRq, arrayCGH - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 22_24 c.4627+25435_4987+660del r.(?) p.(?) - Paternal (inferred) - pathogenic g.216259402_216323160del g.216086060_216149818del - - USH2A_000095 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/+ 22_24 c.4627+25435_4987+660del r.(?) p.(?) - Maternal (inferred) - pathogenic g.216259402_216323160del g.216086060_216149818del - - USH2A_000095 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+/. 21i_24i c.4627+25435_4987+660del r.(4627_4987del) p.(Gly1543_Pro1662del) - Parent #2 ACMG pathogenic g.216259402_216323160del g.216086060_216149818del - - USH2A_000095 - Journal: Reurink 2021 - - Germline yes - - - - DNA SEQ-NG - gene panel retinal disease W19-0855 Journal: Reurink 2021 - - - Poland - - - - - 1 Janine Reurink
+/. - c.4627+25435_4987+660del r.(?) p.(Gly1543_Pro1662del) - Parent #2 ACMG pathogenic g.216259402_216323160del g.216086060_216149818del USH2A c.4627+25435_4987+660del, p.(Gly1543_Pro1662del) - USH2A_000095 heterozygous PubMed: Reurink 2021 - - Germline yes - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0855 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+?/. 21i_24i c.4627+25435_4987+660del r.(4628_4987del) p.(Gly1543_Pro1662del) - Parent #2 ACMG likely pathogenic g.216259402_216323160del g.216086060_216149818del - - USH2A_000095 - PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease 073243;arRP20 PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+?/. 21i_24i c.4627+25435_4987+660del r.(4628_4987del) p.(Gly1543_Pro1662del) - Parent #2 ACMG likely pathogenic g.216259402_216323160del g.216086060_216149818del - - USH2A_000095 - PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease 071367;DFNB2 PubMed: de Bruijn 2023, PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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