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     

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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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Disease     

ID_report     

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Owner     
+/+ 22-23 c.4628-15914_4885+472del r.? p.(Ile1544_Gly1629del) Laminin G-like 1 (1517-1709) Maternal (confirmed) - pathogenic g.216261884_216286470del g.216088542_216113128del - - USH2A_000798 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/. - c.4628-15914_4885+472del r.spl p.(Ile1544_Gly1629del) - Maternal (confirmed) - pathogenic g.216261884_216286470del g.216088542_216113128del USH2A exon 22–23 deleted c.4628-15914_4885+472del, p.(Ile1544_Gly1629de - USH2A_000798 - PubMed: Steele-Stallard 2013 - - Germline yes - - - - DNA, RNA MLPA, arrayCGH, PCR, RT-PCR, SEQ - RNA isolated from nasal epithelial cells retinal disease 151_II:1 PubMed: Steele-Stallard 2013 proband of family 151_II:1 F - United Kingdom (Great Britain) white - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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