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     

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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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Disease     

ID_report     

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Owner     
-?/? 33 c.6341C>T r.(?) p.(Thr2114Ile) Fibronectin type-III 7 (2052-2138) Parent #2 ACMG likely benign g.216173889G>A g.216000547G>A - - USH2A_000111 Heterozygous PubMed: Baux 2007, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
-/? 33 c.6341C>T r.(?) p.(Thr2114Ile) Fibronectin type-III 7 (2052-2138) Paternal (inferred) ACMG likely benign g.216173889G>A g.216000547G>A - - USH2A_000111 Homozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/? 33 c.6341C>T r.(?) p.(Thr2114Ile) Fibronectin type-III 7 (2052-2138) Maternal (inferred) ACMG likely benign g.216173889G>A g.216000547G>A - - USH2A_000111 Homozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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