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)     

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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     

Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Panel size     

Owner     
?/. - c.13514A>G r.(?) p.(Tyr4505Cys) - Unknown - VUS g.215847739T>C g.215674397T>C - - USH2A_001316 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.13514A>G r.(?) p.(Tyr4505Cys) - Unknown - VUS g.215847739T>C g.215674397T>C USH2A c.13514A>G, p.Tyr4505Cys - USH2A_001316 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2865_004450 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
?/. - c.13514A>G r.(?) p.(Tyr4505Cys) - Both (homozygous) - VUS g.215847739T>C g.215674397T>C c.13514A>G, p.Tyr4505Cys - USH2A_001316 homozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2945_004530 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
?/. - c.13514A>G r.(?) p.(Tyr4505Cys) - Both (homozygous) - VUS g.215847739T>C g.215674397T>C c.13514A>G, p.Tyr4505Cys - USH2A_001316 homozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2945_004530 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
?/. 63 c.13514A>G r.(?) p.(Tyr4505Cys) - Parent #2 ACMG VUS g.215847739T>C g.215674397T>C USH2A c.13514A>G, p.Y4505C - USH2A_001316 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF1120 PubMed: Zhu 2021 family 157, patient SRF1120 F - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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