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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AscendingDNA change (cDNA)     

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+/+ 58 c.11328T>G r.(?) p.(Tyr3776*) Fibronectin type-III 23 (3768-3862) Parent #2 - pathogenic g.215931998A>C g.215758656A>C - - USH2A_000534 Heterozygous; Probable pathogenic PubMed: Nakanishi 2011 - - Germline - 0/64 controls +BfaI;+CviKI_1; - - DNA SEQ - - USH2 - PubMed: Nakanishi 2011 Proband F - Japan - - - - - 1 Anne-Françoise Roux
+/. - c.11328T>G r.(?) p.(Tyr3776*) - Unknown - pathogenic g.215931998A>C g.215758656A>C - - USH2A_000534 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs749726310 Germline - 3/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 3 Yoshito Koyanagi
+?/. - c.11328T>G r.(?) p.(Tyr3776*) - Unknown ACMG likely pathogenic (recessive) g.215931998A>C g.215758656A>C - - USH2A_000534 ACMG PVS1, PM2 PubMed: Kim 2022, Journal: Kim 2022 - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - DFNA SB121-213 PubMed: Kim 2022, Journal: Kim 2022 - - - Korea, South (Republic) - - - - - 1 So Young Kim
?/. - c.11328T>G r.(?) p.(Tyr3776Ter) - Unknown ACMG VUS g.215931998A>C g.215758656A>C USH2A c.T11328G, p.Y3776X - USH2A_000534 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 77 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
+?/. - c.11328T>G r.(?) p.(Tyr3776*) - Parent #2 - likely pathogenic g.215931998A>C g.215758656A>C USH2A c.11328T>G, p.(Tyr3776*) - USH2A_000534 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
+/. - c.11328T>G r.(?) p.(Tyr3776Ter) - Unknown ACMG pathogenic g.215931998A>C g.215758656A>C - - USH2A_000534 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Ma, D. J. et al., 2021; PubMed: Inaba, A. et al., 2020 - rs749726310 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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