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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+?/? 60 c.11594C>A r.(?) p.(Ala3865Glu) Fibronectin type-III 24 (3863-3960) Unknown ACMG VUS g.215914834G>T g.215741492G>T - - USH2A_001030 Heterozygous; Possibly pathogenic PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Germany - - - - - 1 Crystel Bonnet
+?/. - c.11594C>A r.(?) p.(Ala3865Glu) - Parent #1 - likely pathogenic g.215914834G>T g.215741492G>T USH2A, variant 1: c.12892T>A/p.Y4298N, variant 2: c.11594C>A/p.A3865E - USH2A_001030 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 361 PubMed: Weisschuh 2020 Filing key number: 120, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
?/. - c.11594C>A r.(?) p.(Ala3865Glu) - Unknown ACMG VUS g.215914834G>T g.215741492G>T - - USH2A_001030 ACMG GN005 criteria: PM2_P PubMed: Weisschuh, N. et al., 2020 - rs1064797132 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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