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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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Re-site     

VIP     

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Disease     

ID_report     

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Owner     
+/+ 03i c.651+1G>A r.spl p.? - Unknown - pathogenic g.216591855C>T g.216418513C>T - - USH2A_000645 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - -BspMI;-HphI;-BfuAI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.651+1G>A r.spl p.(?) - Unknown - likely pathogenic g.216591855C>T g.216418513C>T c.651+1G>A - USH2A_000645 heterozygous PubMed: Gao 2019 - - Germline ? - - - - DNA SEQ-NG - - retinal disease RD18040292_A PubMed: Gao 2019 - ? - China - - - - - 1 LOVD
+/. - c.651+1G>A r.(?) p.(?) - Maternal (confirmed) ACMG pathogenic g.216591855C>T - - - USH2A_000645 - PubMed: Mansard et al, 2021 - rs1553257761 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. - c.651+1G>A r.spl p.? - Unknown ACMG pathogenic g.216591855C>T g.216418513C>T - - USH2A_000645 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Mansard, L. et al., 2021 - rs1553257761 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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