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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-/? 53 c.10465G>A r.(?) p.(Ala3489Thr) Fibronectin type-III 20 (3499-3585) Unknown ACMG likely benign g.215956200C>T g.215782858C>T - - USH2A_000776 Heterozygous; polymorphism PubMed: Glöckle 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +HpyCH4III;-MwoI; - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+?/. - c.10465G>A r.(?) p.(Ala3489Thr) - Parent #1 - likely pathogenic g.215956200C>T g.215782858C>T USH2A, variant 1: c.9424G>T/p.G3142*, variant 2: c.10465G>A/p.A3489T - USH2A_000776 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET3 targeted sequencing panel - see paper retinal disease 1094 PubMed: Weisschuh 2020 Filing key number: 731, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
?/. - c.10465G>A r.(?) p.(Ala3489Thr) - Unknown ACMG VUS g.215956200C>T g.215782858C>T - - USH2A_000776 ACMG GN005 criteria: PM2_P PM3_P BP4_P PubMed: Weisschuh, N. et al., 2020 - rs1553261464 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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