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.

13 entries on 1 page. Showing entries 1 - 13.
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Effect     

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AscendingDNA change (cDNA)     

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+/+ 36 c.6862G>T r.(?) p.(Glu2288*) Fibronectin type-III 9 (2241-2325) Unknown - pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -Hpy188I;-DdeI;-BspCNI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 36 c.6862G>T r.(?) p.(Glu2288*) Fibronectin type-III 9 (2241-2325) Unknown - pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -Hpy188I;-DdeI;-BspCNI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 36 c.6862G>T r.(?) p.(Glu2288*) Fibronectin type-III 9 (2241-2325) Maternal (confirmed) - pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -Hpy188I;-DdeI;-BspCNI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 36 c.6862G>T r.(?) p.(Glu2288*) Fibronectin type-III 9 (2241-2325) Unknown - pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls -Hpy188I;-DdeI;-BspCNI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 36 c.6862G>T r.(?) p.(Glu2288*) Fibronectin type-III 9 (2241-2325) Paternal (inferred) - pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 Homozygous PubMed: Yan 2009 - - Germline - - -Hpy188I;-DdeI;-BspCNI; - - DNA SEQ - - USH2 - PubMed: Yan 2009 Proband M - United States - - - - - 1 Anne-Françoise Roux
+/+ 36 c.6862G>T r.(?) p.(Glu2288*) Fibronectin type-III 9 (2241-2325) Maternal (inferred) - pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 Homozygous PubMed: Yan 2009 - - Germline - - -Hpy188I;-DdeI;-BspCNI; - - DNA SEQ - - USH2 - PubMed: Yan 2009 Proband M - United States - - - - - 1 Anne-Françoise Roux
+/+ 36 c.6862G>T r.(?) p.(Glu2288*) Fibronectin type-III 9 (2241-2325) Parent #1 - pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.6862G>T r.(?) p.(Glu2288*) - Unknown - likely pathogenic g.216144062C>A g.215970720C>A c.2299delG p.(Glu767Serfs*21), c.6862G>T p.(Glu2288*) - USH2A_000234 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 035 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+?/. - c.6862G>T r.(?) p.(Glu2288*) - Unknown - likely pathogenic g.216144062C>A g.215970720C>A USH2A;NM_206933.2;c.[6862G>T];[3407G>A];p.[(Glu2288*)];[(Ser1136Asn)] - USH2A_000234 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.6862G>T r.(?) p.(Glu2288*) - Unknown - pathogenic g.216144062C>A g.215970720C>A c.6862G>T, p.Glu2288Ter - USH2A_000234 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 184-148 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. - c.6862G>T r.(?) p.(Glu2288*) - Maternal (confirmed) - pathogenic g.216144062C>A g.215970720C>A USH2A c.6862G>T, p.(Glu2288*) - USH2A_000234 - PubMed: Steele-Stallard 2013 - - Germline yes - - - - DNA MLPA, arrayCGH, PCR, SEQ - - retinal disease 46_II:1 PubMed: Steele-Stallard 2013 proband of family 46_II:1 F - United Kingdom (Great Britain) white - - - - 1 LOVD
+?/. - c.6862G>T r.(?) p.(Glu2288*) - Parent #1 - likely pathogenic g.216144062C>A g.215970720C>A USH2A c.6862G>T, p.(Glu2288) - USH2A_000234 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.6862G>T r.(?) p.(Glu2288Ter) - Unknown ACMG pathogenic g.216144062C>A g.215970720C>A - - USH2A_000234 ACMG GN005 criteria: PVS1_VS 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; PubMed: Yan, D. et al., 2009 - rs398124619 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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