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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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+/+ 20 c.4384del r.(?) p.(Thr1462Leufs*2) Fibronectin type-III 4 (1367-1462) Paternal (inferred) - pathogenic g.216363579del g.216190237del 4382delA - USH2A_000790 Homozygous; Mutation PubMed: Huang 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Proband F - China - - - - - 1 Anne-Françoise Roux
+/+ 20 c.4384del r.(?) p.(Thr1462Leufs*2) Fibronectin type-III 4 (1367-1462) Maternal (inferred) - pathogenic g.216363579del g.216190237del 4382delA - USH2A_000790 Homozygous; Mutation PubMed: Huang 2013 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Proband F - China - - - - - 1 Anne-Françoise Roux
+/. - c.4384del r.(?) p.(Thr1462Leufs*2) - Unknown ACMG pathogenic g.216363579del g.216190237del USH2A c.4384del(;)5329C>T, V1: c.4384delA, (p.Thr1462LeufsTer2) - USH2A_000790 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F219 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+/. 20 c.4384del r.(?) p.(Thr1462Leufs*2) - Parent #1 ACMG pathogenic g.216363579del g.216190237del USH2A c.4384delA, p.(Thr1462Leufs*2) - USH2A_000790 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 842 PubMed: Zhu 2021 family 232, patient 842 M - China - - - - - 1 LOVD
+/. 20 c.4384del r.(?) p.(Thr1462Leufs*2) - Parent #2 ACMG pathogenic g.216363579del g.216190237del USH2A c.4384delA, p.(Thr1462Leufs*2) - USH2A_000790 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 569 PubMed: Zhu 2021 family 230, patient 569 M - China - - - - - 1 LOVD
+/. - c.4384del r.(?) p.(Thr1462LeufsTer2) - Unknown ACMG pathogenic g.216363579del g.216190237del 4384delA - USH2A_000790 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Huang, X. F. et al., 2013; PubMed: Shu, H. R. et al., 2015 - rs2034687946 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.4384delA r.(?) p.(Thr1462LeufsTer2) - Unknown - pathogenic g.216363579del g.216190237del USH2A c.4384del(;)5329C>T; p.(Thr1462LeufsTer2) - USH2A_000790 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0; GnomAD_exome_East: 0; GnomAD_All: 0 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F219 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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