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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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VIP     

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Disease     

ID_report     

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Owner     
+?/? 6 c.850G>A r.(?) p.(Glu284Lys) Laminin N-terminal (271-517) Unknown ACMG VUS g.216498940C>T g.216325598C>T - - USH2A_000093 Heterozygous PubMed: Baux 2007, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.850G>A r.(?) p.(Glu284Lys) - Parent #1 - likely pathogenic g.216498940C>T g.216325598C>T USH2A c.850G>A, p.(Glu284Lys) - USH2A_000093 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.850G>A r.(?) p.(Glu284Lys) - Unknown ACMG VUS g.216498940C>T g.216325598C>T - - USH2A_000093 ACMG GN005 criteria: PM2_P PM3_P PubMed: Inaba, A. 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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