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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+?/? 30 c.5932C>T r.(?) p.(Pro1978Ser) Fibronectin type-III 6 (1954-2051) Unknown ACMG VUS g.216243560G>A g.216070218G>A - - USH2A_000414 Heterozygous; possibly deleterious PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs75698489 Germline - - - - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - - United States - - - - - 1 Anne-Françoise Roux
?/. - c.5932C>T r.(?) p.(Pro1978Ser) - Unknown ACMG VUS g.216243560G>A g.216070218G>A USH2A:NM_206933 c.C5932T, p.P1978S - USH2A_000414 heterozygous, individual solved, variant non-causal PubMed: Rodriguez-Munoz 2020 - - Germline ? - - - - DNA SEQ-NG-I blood - retinal disease RPN-282 PubMed: Rodriguez-Munoz 2020 family fRPN-125, proband F - Spain - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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