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     

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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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Re-site     

VIP     

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Tissue     

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Disease     

ID_report     

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VIP     

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Owner     
+/+ 47 c.9259-2402_9371+1537del r.? p.(Val3087Ilefs*5) Fibronectin type-III 17 (3020-3105);Fibronectin type-III 18 (3110-3200) Paternal (confirmed) - pathogenic g.216009801_216013852del g.215836459_215840510del - - USH2A_000729 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA arrayCGH, MLPA, SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 47 c.9259-2402_9371+1537del r.? p.(Val3087Ilefs*5) Fibronectin type-III 17 (3020-3105), Fibronectin type-III 18 (3110-3200) Parent #2 - pathogenic g.216009801_216013852del g.215836459_215840510del - - USH2A_000729 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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