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.

7 entries on 1 page. Showing entries 1 - 7.
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+?/? 28 c.5603T>G r.(?) p.(Phe1868Cys) Laminin G-like 2 (1714-1891) Unknown ACMG VUS g.216246612A>C g.216073270A>C - - USH2A_000650 Heterozygous; UV2 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/96 controls +Hpy166II;+CviQI;+BsrGI;+RsaI;-Tsp509I;-ApoI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. - c.5603T>G r.(?) p.(Phe1868Cys) - Unknown - pathogenic (recessive) g.216246612A>C - 1:216246612A>C ENST00000307340.3:c.5603T>G (Phe1868Cys) - USH2A_000650 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease B240282 PubMed: Carss 2017 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.5603T>G r.(?) p.(Phe1868Cys) - Parent #2 - likely pathogenic (recessive) g.216246612A>C g.216073270A>C - - USH2A_000650 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam2PatTO2 PubMed: Eandi 2017 2-generation family, 2 affected M - Italy - - - - - 2 LOVD
+?/. - c.5603T>G r.(?) p.(Phe1868Cys) - Parent #2 - likely pathogenic (recessive) g.216246612A>C g.216073270A>C - - USH2A_000650 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam2PatTO3 PubMed: Eandi 2017 brother M - Italy - - - - - 1 LOVD
+?/. - c.5603T>G r.(?) p.(Phe1868Cys) - Parent #2 - likely pathogenic g.216246612A>C g.216073270A>C USH2A c.5603T>G, p.F1868C - USH2A_000650 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 153 PubMed: Jauregui 2020 - M - (United States) white - - - - 1 LOVD
+?/. - c.5603T>G r.(?) p.(Phe1868Cys) - Parent #1 - likely pathogenic g.216246612A>C g.216073270A>C USH2A c.5603T>G - USH2A_000650 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 22 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
?/. - c.5603T>G r.(?) p.(Phe1868Cys) - Unknown ACMG VUS g.216246612A>C g.216073270A>C - - USH2A_000650 ACMG GN005 criteria: PM2_P PM3_M PP1_P PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Eandi, C. M. et al., 2017; PubMed: Jauregui, R. et al., 2020 - rs1553298240 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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