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     

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AscendingDNA change (cDNA)     

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-?/? 2 c.188G>A r.(?) p.(Arg63Gln) - Unknown ACMG likely benign g.216595491C>T g.216422149C>T - - USH2A_000791 Heterozygous; Mutation PubMed: Yang 2013, USMA missense analysis, missense variant in MSV3d - - Germline - 0/400 controls - - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Yang 2013 Proband - age < 6 yrs - - China - - - - - 1 Anne-Françoise Roux
-?/. - c.188G>A r.(?) p.(Arg63Gln) - Unknown ACMG likely benign g.216595491C>T g.216422149C>T - - USH2A_000791 ACMG GN005 criteria: BP4_P PubMed: Yang, T. et al., 2013 - rs369806765 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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