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     

Classification method     

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     

Methylation     

Template     

Technique     

Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Panel size     

Owner     
+?/. - c.13531G>A r.(?) p.(Ala4511Thr) - Parent #2 - likely pathogenic g.215847722C>T g.215674380C>T - - USH2A_001896 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 86 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. 63 c.13531G>A r.(?) p.(Ala4511Thr) - Unknown - likely pathogenic g.215847722C>T g.215674380C>T USH2A Ex.54 c.10712C>T p.(Thr3571Met), Ex.63 c.13531G>A p.(Ala4511Thr) - USH2A_001896 compound heterozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA SEQ-NG-I - - retinal disease RP-0973 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
?/. - c.13531G>A r.(?) p.(Ala4511Thr) - Unknown ACMG VUS g.215847722C>T g.215674380C>T - - USH2A_001896 ACMG GN005 criteria: PM2_P PubMed: Del Pozo-Valero, M. et al., 2022 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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