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     

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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Re-site     

VIP     

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Template     

Technique     

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Disease     

ID_report     

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Owner     
+/. 41 c.7698T>A r.(?) p.(Tyr2566*) - Maternal (confirmed) - pathogenic g.216062293A>T g.215888951A>T USH2A c.7698T>A, p.Y2566X - USH2A_002549 heterozygous PubMed: Qu 2020 - - Germline yes - - - - DNA SEQ-NG, SEQ blood 103 known RD genes panel USH USH F1-II-1 PubMed: Qu 2020 - M - - - - - - - 1 LOVD
+?/. 41 c.7698T>A r.(?) p.(Tyr2566*) - Parent #2 ACMG likely pathogenic g.216062293A>T g.215888951A>T USH2A c.7698T>A, p.Tyr2566* - USH2A_002549 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 8 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
+/. - c.7698T>A r.(?) p.(Tyr2566*) - Parent #2 - pathogenic g.216062293A>T g.215888951A>T USH2A c.7698T>A, p.Tyr2566* - USH2A_002549 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH DP18126966 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
+/. 41 c.7698T>A r.(?) p.(Tyr2566*) - Parent #2 ACMG pathogenic g.216062293A>T g.215888951A>T USH2A c.7698T>A, p.Y2566* - USH2A_002549 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 26460994 PubMed: Zhu 2021 family 220, patient 26460994 F - China - - - - - 1 LOVD
+/. 41 c.7698T>A r.(?) p.(Tyr2566*) - Parent #2 ACMG pathogenic g.216062293A>T g.215888951A>T USH2A c.7698T>A, p.Y2566* - USH2A_002549 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF502 PubMed: Zhu 2021 family 70, patient SRF502 M - China - - - - - 1 LOVD
+?/. - c.7698T>A r.(?) p.(Tyr2566Ter) - Unknown ACMG likely pathogenic g.216062293A>T g.215888951A>T - - USH2A_002549 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Gao, F. J. et al., 2021; PubMed: Qu, L. H. et al., 2020; PubMed: Meng, X. et al., 2021 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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