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.

10 entries on 1 page. Showing entries 1 - 10.
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+?/? 17 c.3407G>A r.(?) p.(Ser1136Asn) Fibronectin type-III 1 (1058-1143) Unknown ACMG VUS g.216373373C>T g.216200031C>T - - USH2A_000644 Heterozygous; UV4 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/878 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 17 c.3407G>A r.(?) p.(Ser1136Asn) Fibronectin type-III 1 (1058-1143) Parent #2 ACMG VUS g.216373373C>T g.216200031C>T - - USH2A_000644 Heterozygous; mutation PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Denmark - - - - - 1 Crystel Bonnet
+?/. - c.3407G>A r.(?) p.(Ser1136Asn) - Parent #2 - likely pathogenic g.216373373C>T g.216200031C>T - - USH2A_000644 - PubMed: Huang 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease RP-166 PubMed: Huang 2017 patient - - China - - - - - 1 LOVD
+/. 17 c.3407G>A r.(?) p.(Ser1136Asn) - Parent #2 - pathogenic (recessive) g.216373373C>T g.216200031C>T - - USH2A_000644 - PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-52 PubMed: Dad 2016 family, 2 affeted F no Denmark - - - - - 2 LOVD
+/. 17 c.3407G>A r.(?) p.(Ser1136Asn) - Parent #2 - pathogenic (recessive) g.216373373C>T g.216200031C>T - - USH2A_000644 - PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-52a PubMed: Dad 2016 - M no Denmark - - - - - 1 LOVD
+?/. - c.3407G>A r.(?) p.(Ser1136Asn) - Unknown - likely pathogenic g.216373373C>T g.216200031C>T - - USH2A_000644 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 13003723 PubMed: Ellingford 2016 patient - - - - - - - - 1 LOVD
+?/. - c.3407G>A r.(?) p.(Ser1136Asn) - Unknown ACMG likely pathogenic g.216373373C>T g.216200031C>T USH2A c.14911C>T, p.(Arg4971*), c.3407G>A, p.(Ser1136Asn) - USH2A_000644 - PubMed: Jespersgaar 2019 - - Germline ? - - - - DNA SEQ-NG-I blood 125 genes associated with inherited retinal disorders, see paper supplemental data retinal disease 280 PubMed: Jespersgaar 2019 - ? - Denmark - - - - - 1 LOVD
+?/. - c.3407G>A r.(?) p.(Ser1136Asn) - Unknown - likely pathogenic g.216373373C>T g.216200031C>T USH2A;NM_206933.2;c.[6862G>T];[3407G>A];p.[(Glu2288*)];[(Ser1136Asn)] - USH2A_000644 compound heterozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 176 genes panel retinal disease 9 PubMed: Jiman 2020 - F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.3407G>A r.(?) p.(Ser1136Asn) - Parent #2 - likely pathogenic g.216373373C>T g.216200031C>T USH2A c.3407G>A, p.(Ser1136Asn) - USH2A_000644 heterozygous PubMed: Molina-Ramirez 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 14 patients: 105-gene panel, 13 samples: 176-gene panel using previously described method (O', Sullivan J et al. 2012) USH 15014727 PubMed: Molina-Ramirez 2020 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.3407G>A r.(?) p.(Ser1136Asn) - Unknown ACMG likely pathogenic g.216373373C>T g.216200031C>T - - USH2A_000644 ACMG GN005 criteria: PM2_P PM3_M PubMed: Molina-Ramirez, L. P. et al., 2020; PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012 - rs483353055 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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