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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+?/? 35 c.6746C>A r.(?) p.(Ala2249Asp) Fibronectin type-III 9 (2241-2325) Parent #2 ACMG VUS g.216166421G>T g.215993079G>T - - USH2A_000191 Heterozygous PubMed: Najera 2002, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Najera 2002 Proband - - Spain - - - - - 1 Jose Maria Millan
?/. - c.6746C>A r.(?) p.(Ala2249Asp) - Unknown ACMG VUS g.216166421G>T g.215993079G>T - - USH2A_000191 ACMG GN005 criteria: PM2_P PM3_M PubMed: Aller, E. et al., 2006 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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