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     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Reference     

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Owner     
-?/? 37 c.7061G>A r.(?) p.(Arg2354His) Fibronectin type-III 10 (2328-2432) Parent #2 ACMG likely benign g.216138718C>T g.215965376C>T - - USH2A_000178 Heterozygous PubMed: Aller 2006, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Aller 2006 Proband M - Spain - - - - - 1 Jose Maria Millan
?/. - c.7061G>A r.(?) p.(Arg2354His) - Unknown - VUS g.216138718C>T g.215965376C>T - - USH2A_000178 - - ClinVar-000803389 - Germline yes - - - - DNA SEQ-NG-I - WES LCA2 RPCR-XIV-2 - 2 generations- 1(F) and 1(M), both parents are confirmed carriers, this patient was also diagnosed with Ushers syndrome, parents are unknown carriers- no sequencing done for USH2A for parents M no Costa Rica - - - - none 2 Bailey Glen
-?/. - c.7061G>A r.(?) p.(Arg2354His) - Unknown ACMG likely benign g.216138718C>T g.215965376C>T - - USH2A_000178 ACMG GN005 criteria: PubMed: Aller, E. et al., 2006 - rs201386640 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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