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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AscendingDNA change (cDNA)     

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-/? 71 c.15364T>C r.(?) p.(Cys5122Arg) Cytoplasmic (5064-5202) Unknown ACMG likely benign g.215802311A>G g.215628969A>G - - USH2A_000783 Heterozygous; polymorphism PubMed: Glöckle 2014, USMA missense analysis, missense variant in MSV3d - rs111033402 Germline - - +AflIII;+ApaLI;+BaeGI;-CviAII;-FatI;-NlaIII; - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - the gene RDH12 is responsible - - - - - - - - 1 Anne-Françoise Roux
-/? 71 c.15364T>C r.(?) p.(Cys5122Arg) Cytoplasmic (5064-5202) Parent #2 ACMG likely benign g.215802311A>G g.215628969A>G - - USH2A_000783 Heterozygous; Possibly pathogenic PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - rs111033402 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
?/. - c.15364T>C r.(?) p.(Cys5122Arg) - Unknown ACMG VUS g.215802311A>G g.215628969A>G - - USH2A_000783 ACMG GN005 criteria: BP4_P PubMed: Bonnet, C. et al., 2016 - rs111033402 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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