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.

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Disease     

ID_report     

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Owner     
+/+ 16i c.3317-2A>G r.spl p.? - Parent #2 - pathogenic g.216373465T>C g.216200123T>C - - USH2A_000125 Heterozygous PubMed: Baux 2007 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 16i c.3317-2A>G r.spl p.? - Maternal (confirmed) - pathogenic g.216373465T>C g.216200123T>C - - USH2A_000125 Heterozygous PubMed: Baux 2014 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+/+ 16i c.3317-2A>G r.spl p.? - Unknown - pathogenic g.216373465T>C g.216200123T>C - - USH2A_000125 Heterozygous; likely pathogenic PubMed: Glöckle 2014 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Glöckle 2014 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 16i c.3317-2A>G r.spl p.? - Parent #2 - pathogenic g.216373465T>C g.216200123T>C - - USH2A_000125 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+?/. - c.3317-2A>G r.spl p.(?) - Parent #1 - likely pathogenic g.216373465T>C g.216200123T>C USH2A, variant 1: c.3317-2A>G/p.?, variant 2: c.10721G>T/p.G3475V - USH2A_000125 possibly solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET2 targeted sequencing panel - see paper retinal disease 1110 PubMed: Weisschuh 2020 Filing key number: 750, sporadic retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
+/. - c.3317-2A>G r.spl p.? - Unknown ACMG pathogenic g.216373465T>C g.216200123T>C - - USH2A_000125 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PP1_S PubMed: Bonnet, C. et al., 2016; PubMed: Glockle, N. et al., 2014; PubMed: Weisschuh, N. et al., 2020 - rs2034951427 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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