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.

9 entries on 1 page. Showing entries 1 - 9.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Segregation     

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Re-site     

VIP     

Methylation     

Template     

Technique     

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Disease     

ID_report     

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Panel size     

Owner     
+/+ 5-1 c.785-6636_1840+208del r.? p.(Leu263_Gly614del) Laminin N-terminal (271-517);Laminin EGF-like 1 (518-574);Laminin EGF-like 2 (575-640) Maternal (confirmed) - pathogenic g.216465309_216507632del g.216291967_216334290del - - USH2A_000739 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 5-1 c.785-6636_1840+208del r.? p.? Laminin N-terminal (271-517);Laminin EGF-like 1 (518-574);Laminin EGF-like 2 (575-640) Paternal (confirmed) - pathogenic g.216465309_216507632del g.216291967_216334290del - - USH2A_000739 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA arrayCGH, SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 5-1 c.785-6636_1840+208del r.? p.(Leu263_Gly614del) Laminin N-terminal (271-517), Laminin EGF-like 1 (518-574), Laminin EGF-like 2 (575-640) Parent #2 - pathogenic g.216465309_216507632del g.216291967_216334290del - - USH2A_000739 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq, arrayCGH - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+/+ 5-1 c.785-6636_1840+208del r.? p.(Leu263_Gly614del) Laminin N-terminal (271-517), Laminin EGF-like 1 (518-574), Laminin EGF-like 2 (575-640) Paternal (inferred) - pathogenic g.216465309_216507632del g.216291967_216334290del - - USH2A_000739 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA arrayCGH, SEQ - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 5-1 c.785-6636_1840+208del r.? p.(Leu263_Gly614del) Laminin N-terminal (271-517), Laminin EGF-like 1 (518-574), Laminin EGF-like 2 (575-640) Maternal (inferred) - pathogenic g.216465309_216507632del g.216291967_216334290del - - USH2A_000739 Homozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA arrayCGH, SEQ - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.785-6636_1840+208del r.(?) p.(Leu263_Gly614del) - Maternal (confirmed) ACMG pathogenic g.216465309_216507632del - - - USH2A_000739 - PubMed: Mansard et al, 2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.785-6636_1840+208del r.(?) p.(?) - Parent #1 - pathogenic g.216465309_216507632del g.216291967_216334290del USH2A allele 1: Exon 5-10 deletion, g.216465309_216507632del, allele 2: none - USH2A_000739 the breakpoints of this deletion are different than these of the cited ClinVar variant; c.DNA annotation based on publication boundaries PubMed: Austin-Tse 2018 SCV000205103 - Germline yes - - - - DNA SEQ-NG-I, MLPA - sequenced by dideoxy sequencing or hearing loss gene panel by either microarray-based resequencing or oligonucleotide-based target capture followed by next generation sequencing using Illumina HiSeq2000 or MiSeq instrument USH D-1 PubMed: Austin-Tse 2018 Discovery Cohort ? - United States - - - - - 1 LOVD
+?/. 4i_10i c.785-6636_1840+208del r.(785_1840del) p.? - Parent #2 ACMG likely pathogenic g.216465309_216507632del g.216291967_216334290del - - USH2A_000739 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH34 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+?/. 4i_10i c.785-6636_1840+208del r.(?) p.(Leu263_Gly614del) - Parent #1 ACMG likely pathogenic (recessive) g.216465309_216507632del g.216291967_216334290del - - USH2A_000739 - PubMed: De Bruijn 2023 - - Germline - - - - - DNA SEQ-NG blood Published as WGS USH2 073258 PubMed: de Bruijn 2023 - - - - - - - - - 1 Suzanne de Bruijn
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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