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.

2 entries on 1 page. Showing entries 1 - 2.
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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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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
+?/. - c.11700C>A r.(?) p.(Tyr3900*) - Unknown - likely pathogenic (recessive) g.215914728G>T - 1:215914728G>T ENST00000307340.3:c.11700C>A (Tyr3900Ter) - USH2A_001806 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G007707 PubMed: Carss 2017 - M - United Kingdom (Great Britain) Europe - - - - 1 LOVD
+?/. - c.11700C>A r.(?) p.(Tyr3900*) - Both (homozygous) - likely pathogenic g.215914728G>T g.215741386G>T USH2A c.11700C>A - USH2A_001806 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 9 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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