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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+/+ 40 c.7524del r.(?) p.(Arg2509Glyfs*19) Fibronectin type-III 11 (2435-2528) Parent #2 - pathogenic g.216073489del g.215900147del 7522delT - USH2A_000547 Heterozygous; Pathogenic PubMed: Bonnet 2011 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 40 c.7524del r.(?) p.(Arg2509Glyfs*19) Fibronectin type-III 11 (2435-2528) Unknown - pathogenic g.216073489del g.215900147del 7524delT - USH2A_000547 Heterozygous; mutation PubMed: Krawitz 2014 - - Germline - - none - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband M - Germany - - - - - 1 Peter Krawitz
+/+ 40 c.7524del r.(?) p.(Arg2509Glyfs*19) Fibronectin type-III 11 (2435-2528) Parent #1 - pathogenic g.216073489del g.215900147del 7524delT - USH2A_000547 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 40 c.7524del r.(?) p.(Arg2509Glyfs*19) Fibronectin type-III 11 (2435-2528) Parent #1 - pathogenic g.216073489del g.215900147del 7524delT - USH2A_000547 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/. - c.7524del r.(?) p.(Arg2509GlyfsTer19) - Unknown - pathogenic g.216073487del - - - USH2A_000547 - - - - Unknown - - - - - DNA SEQ - - ? - - - M - - - - - - - 1 IMGAG
+/. 40 c.7524del r.(?) p.(Arg2509Glyfs*19) - Parent #2 - pathogenic (recessive) g.216073489del g.215900147del 7524delT - USH2A_000547 - PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-34 (D63) PubMed: Dad 2016 - F no Denmark - - - - - 1 LOVD
+?/. - c.7524del r.(?) p.(Arg2509Glyfs*19) - Parent #1 - likely pathogenic g.216073489del g.215900147del USH2A c.7524del, p.R2509GfsX19 - USH2A_000547 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 106 PubMed: Jauregui 2020 - F - (United States) white - - - - 1 LOVD
+/. - c.7524del r.(?) p.(Arg2509GlyfsTer19) - Unknown ACMG pathogenic g.216073489del g.215900147del 7524delT - USH2A_000547 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Bonnet, C. et al., 2016; PubMed: Ganapathi, M. et al., 2022; PubMed: Kamenarova, K. et al., 2022; PubMed: Jauregui, R. et al., 2020 - rs751176116 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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