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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+?/? 17 c.3596_3598del r.(?) p.(Glu1199del) Fibronectin type-III 1 (1058-1143) Paternal (confirmed) ACMG VUS g.216373183_216373185del g.216199841_216199843del 3595_3597delGAA, p.E1119del - USH2A_000861 Heterozygous; very likely pathogenic PubMed: Zhao 2014 - - De novo - 0/400 controls - - - DNA SEQ - - RPar - PubMed: Zhao 2014 Proband M - Japan - - - - - 1 Anne-Françoise Roux
+/. - c.3596_3598del r.(?) p.(Glu1199del) - Unknown - pathogenic g.216373183_216373185del g.216199841_216199843del - - USH2A_000861 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - - Germline - 5/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 5 Yoshito Koyanagi
+?/. - c.3596_3598del r.(?) p.(Glu1199del) - Parent #1 - likely pathogenic g.216373183_216373185del g.216199841_216199843del USH2A c.3596_3598delAAG, p.(Glu1199del) - USH2A_000861 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
+?/. - c.3596_3598del r.(?) p.(Glu1199del) - Parent #1 - likely pathogenic g.216373183_216373185del g.216199841_216199843del USH2A c.3596_3598delAAG, p.(Glu1199del) - USH2A_000861 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
+?/. - c.3596_3598del r.(?) p.(Glu1199del) - Parent #2 - likely pathogenic g.216373183_216373185del g.216199841_216199843del USH2A c.3595_3597delGAA, p.(Glu1199del) - USH2A_000861 heterozygous PubMed: Inaba 2020 - - Unknown ? - - - - DNA SEQ-NG-I - panel of 39 (238 patients) or 50 (287 patients) genes retinal disease - PubMed: Inaba 2020 - - - Japan - - - - - 1 LOVD
?/. - c.3596_3598del r.(?) p.(Glu1199del) - Unknown ACMG VUS g.216373183_216373185del g.216199841_216199843del 3596_3598delAAG - USH2A_000861 ACMG GN005 criteria: PM2_P PM3_M PubMed: Zhao, Y. et al., 2014; PubMed: Inaba, A. et al., 2020 - rs1294733964 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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