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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Reference     

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Disease     

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Owner     
+?/. - c.15063_15081delinsGC r.(?) p.(Thr5022Glnfs*150) - Parent #1 - likely pathogenic g.215808017_215808035delinsGC g.215634675_215634693delinsGC USH2A, variant 1: c.7950dup/p.N2651Qfs*10, variant 2: c.15063_15081delinsGC/ p.T5022Qfs*150 - USH2A_002365 solved, compound heterozygous PubMed: Weisschuh 2020 - - Germline yes - - - - DNA SEQ-NG blood RET5 targeted sequencing panel - see paper retinal disease 658 PubMed: Weisschuh 2020 Filing key number: 235, Usher syndrome type 2, no patient Ids, consecutive numbers given F - Germany - - - - - 1 LOVD
+?/. 70 c.15063_15081delinsGC r.(?) p.(Thr5022Glnfs*150) - Unknown - likely pathogenic g.215808017_215808035delinsGC - c.15063_15081delinsGC, p.T5022Qfs*150 - USH2A_002365 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 70 c.15063_15081delinsGC r.(?) p.(Thr5022Glnfs*150) - Unknown - likely pathogenic g.215808017_215808035delinsGC - c.15063-15081delinsGC - USH2A_002365 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. 70 c.15063_15081delinsGC r.(15063_15081delinsgc) p.(Thr5022GlnfsTer150) - Parent #2 ACMG pathogenic g.215808017_215808035delinsGC g.215634675_215634693delinsGC - - USH2A_002365 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH17 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+/. - c.15063_15081delinsGC r.(?) p.(Thr5022GlnfsTer150) - Unknown ACMG pathogenic g.215808017_215808035delinsGC g.215634675_215634693delinsGC - - USH2A_002365 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Wafa, T. T. et al., 2021; PubMed: Weisschuh, N. et al., 2020 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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