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     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 67i c.14791+4A>G r.spl? p.? - Parent #2 - pathogenic g.215820860T>C g.215647518T>C - - USH2A_001074 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - Italy - - - - - 1 Crystel Bonnet
+/. 67i c.14791+4A>G r.spl? p.? - Parent #1 - pathogenic (recessive) g.215820860T>C - - - USH2A_001074 - PubMed: Ivanova 2018 - - Germline - - - - - DNA SEQ-NG-S - - USH2 Pat24 PubMed: Ivanova 2018 Proband F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+?/. - c.14791+4A>G r.spl? p.? - Unknown ACMG likely pathogenic g.215820860T>C - - - USH2A_001074 - PubMed: Mansard 2021 - rs1408904076 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. 67i c.14791+4A>G r.14583_14791del p.Tyr4862Alafs*22 - Unknown ACMG pathogenic g.215820860T>C - - - USH2A_001074 mini-gene splicing assay; changes ACMG to pathogenic PubMed: Reurink 2022, Journal: Reurink 2022 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.14791+4A>G r.spl p.? - Unknown ACMG VUS g.215820860T>C g.215647518T>C - - USH2A_001074 ACMG GN005 criteria: PM2_P PM3_M PP3_P PubMed: Bonnet, C. et al., 2016; PubMed: Mansard, L. et al., 2021 - rs1408904076 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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