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.

6 entries on 1 page. Showing entries 1 - 6.
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+?/? 53 c.10421A>G r.(=) p.(Tyr3474Cys) Fibronectin type-III 19 (3404-3494) Unknown ACMG VUS g.215956244T>C g.215782902T>C - - USH2A_000854 Heterozygous; causative PubMed: Eisenberger 2013, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Eisenberger 2013 Proband M - Germany - - - - - 1 Anne-Françoise Roux
+?/. - c.10421A>G r.(?) p.(Tyr3474Cys) - Unknown - likely pathogenic g.215956244T>C g.215782902T>C USH2A(NM_206933.2):c.10421A>G (p.Y3474C), USH2A(NM_206933.4):c.10421A>G (p.Y3474C) - USH2A_000854 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. 53 c.10421A>G r.(?) p.(Tyr3474Cys) - Unknown - pathogenic g.215956244T>C - c.10421A>G - USH2A_000854 - PubMed: Eisenberger-2013 - - Germline - - - - - DNA SEQ-NG-I, SEQ-NG-R, SEQ blood - retinal disease - PubMed: Eisenberger-2013 - M no Germany - - - - - 1 LOVD
+?/. - c.10421A>G r.(?) p.(Tyr3474Cys) - Parent #1 - likely pathogenic g.215956244T>C g.215782902T>C USH2A, variant 1: c.12234_12235del/p.N4079Wfs*19, variant 2: c.10421A>G/p.Y3474C - USH2A_000854 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET6 targeted sequencing panel - see paper retinal disease 307 PubMed: Weisschuh 2020 Filing key number: 102, Usher syndrome type 2, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
?/. - c.10421A>G r.(?) p.(Tyr3474Cys) - Unknown - VUS g.215956244T>C - USH2A(NM_206933.2):c.10421A>G (p.Y3474C), USH2A(NM_206933.4):c.10421A>G (p.Y3474C) - USH2A_000854 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.10421A>G r.(?) p.(Tyr3474Cys) - Unknown ACMG VUS g.215956244T>C g.215782902T>C - - USH2A_000854 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Weisschuh, N. et al., 2020 - rs749121941 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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