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)     

RNA change     

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P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

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Reference     

ClinVar ID     

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?/. - c.2081G>A r.(?) p.(Cys694Tyr) - Unknown - VUS g.216424331C>T g.216250989C>T USH2A(NM_206933.4):c.2081G>A (p.C694Y) - USH2A_001266 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.2081G>A r.(?) p.(Cys694Tyr) - Unknown - VUS g.216424331C>T g.216250989C>T USH2A(NM_206933.4):c.2081G>A (p.C694Y) - USH2A_001266 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.2081G>A r.(?) p.(Cys694Tyr) - Unknown - pathogenic (recessive) g.216424331C>T - 1:216424331C>T ENST00000307340.3:c.2081G>A (Cys694Tyr) - USH2A_001266 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G001032 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. 12 c.2081G>A r.(?) p.(Cys694Tyr) - Unknown - likely pathogenic g.216424331C>T g.216250989C>T USH2A Ex.12 c.2081G>A p.(Cys694Tyr), Ex.50 c.9799T>C p.(Cys3267Arg), ABCA4: Ex.13 c.1928T>Gp.(Val643Gly) - USH2A_001266 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-2704 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. - c.2081G>A r.(?) p.(Cys694Tyr) - Unknown - likely pathogenic g.216424331C>T g.216250989C>T USH2A c.2081G>A, p.Cys694Tyr - USH2A_001266 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001032 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.2081G>A r.(?) p.(Cys694Tyr) - Parent #1 - likely pathogenic g.216424331C>T g.216250989C>T USH2A c.2081G>A - USH2A_001266 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 52 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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