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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

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AscendingDNA change (cDNA)     

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+/+ 63i c.13811+2T>G r.spl p.? - Unknown - pathogenic g.215847440A>C g.215674098A>C - - USH2A_000751 Heterozygous PubMed: Besnard, Garcia-Garcia 2014 - - Germline - - +MnlI - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Besnard, Garcia-Garcia 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 63i c.13811+2T>G r.spl p.? - Unknown - pathogenic g.215847440A>C g.215674098A>C - - USH2A_000751 Heterozygous PubMed: Aparisi 2014 - - Germline - - +MnlI - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/+ 63i c.13811+2T>G r.spl p.? - Parent #1 - pathogenic g.215847440A>C g.215674098A>C - - USH2A_000751 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.13811+2T>G r.spl p.(?) - Paternal (confirmed) - likely pathogenic g.215847440A>C g.215674098A>C - - USH2A_000751 - PubMed: Perez-Carro 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease RP-1422 PubMed: Perez-Carro 2018 family RP-1422 M no Spain - - - - - 1 LOVD
+/. - c.13811+2T>G r.(?) p.(?) - Unknown ACMG pathogenic g.215847440A>C - - - USH2A_000751 - PubMed: Mansard et al, 2021 - rs766515318 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - ? - - - - - - - 1 Anne-Françoise Roux
+/. - c.13811+2T>G r.(?) p.(?) - Maternal (confirmed) ACMG pathogenic g.215847440A>C - - - USH2A_000751 - PubMed: Mansard et al, 2021 - rs766515318 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.13811+2T>G r.(?) p.(?) - Unknown ACMG pathogenic g.215847440A>C - - - USH2A_000751 - PubMed: Mansard et al, 2021 - rs766515318 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.13811+2T>G r.spl p.? - Unknown ACMG pathogenic g.215847440A>C g.215674098A>C - - USH2A_000751 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Perez-Carro, R. et al., 2018; PubMed: Garcia Bohorquez, B. et al., 2021; PubMed: Mansard, L. et al., 2021; PubMed: Aparisi, M. J. et al., 2014 - rs766515318 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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