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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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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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Re-site     

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Disease     

ID_report     

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Owner     
+/+ 53 c.10450C>T r.(?) p.(Arg3484*) Fibronectin type-III 19 (3404-3494) Paternal (confirmed) - pathogenic g.215956215G>A g.215782873G>A - - USH2A_000475 Heterozygous; Mutation PubMed: Huang 2013 - rs111033379 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 53 c.10450C>T r.(?) p.(Arg3484*) Fibronectin type-III 19 (3404-3494) Paternal (confirmed) - pathogenic g.215956215G>A g.215782873G>A - - USH2A_000475 Heterozygous; Mutation PubMed: Huang 2013 - rs111033379 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Huang 2013 Proband - son of CZ0100120041 M - China - - - - - 1 Anne-Françoise Roux
+/+ 53 c.10450C>T r.(?) p.(Arg3484*) Fibronectin type-III 19 (3404-3494) Parent #2 - pathogenic g.215956215G>A g.215782873G>A - - USH2A_000475 Heterozygous PubMed: Sodi 2014 - rs111033379 Germline - - - - - DNA SEQ - - USH2 - PubMed: Sodi 2014 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+?/. - c.10450C>T r.(?) p.(Arg3484*) - Parent #1 - likely pathogenic g.215956215G>A - - - USH2A_000475 - PubMed: Holtan 2020 - - Germline - 1/899 cases - - - DNA SEQ - - retinal disease - PubMed: Holtan 2020 1 patient with variant in heterozygous or compound heterozygous form - - Norway - - - - - 1 Global Variome, with Curator vacancy
+?/. - c.10450C>T r.(?) p.(Arg3484*) - Parent #2 - likely pathogenic (recessive) g.215956215G>A g.215782873G>A - - USH2A_000475 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam10PatTO12 PubMed: Eandi 2017 2-generation family, 2 affected M - Italy - - - - - 2 LOVD
+?/. - c.10450C>T r.(?) p.(Arg3484*) - Parent #2 - likely pathogenic (recessive) g.215956215G>A g.215782873G>A - - USH2A_000475 - PubMed: Eandi 2017 - - Germline - - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam10PatTO13 PubMed: Eandi 2017 sister F - Italy - - - - - 1 LOVD
+?/. - c.10450C>T r.(?) p.(Arg3484*) - Parent #1 - likely pathogenic g.215956215G>A g.215782873G>A - - USH2A_000475 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 577 PubMed: Stone 2017 family, 2 affected F - (United States) - - - - - 2 LOVD
+?/. - c.10450C>T r.(?) p.(Arg3484*) - Parent #2 - likely pathogenic g.215956215G>A g.215782873G>A - - USH2A_000475 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 572 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+/. - c.10450C>T r.(?) p.(Arg3484*) - Unknown - pathogenic g.215956215G>A g.215782873G>A USH2A c.10450C>T, p.Arg3484Ter - USH2A_000475 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease 160-030 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. 53 c.10450C>T r.(?) p.(Arg3484*) - Unknown - pathogenic (recessive) g.215956215G>A - c.10450C>T - USH2A_000475 - PubMed: Colombo-2020 - rs111033379 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - F no - - - - - - 1 LOVD
+/. - c.10450C>T r.(?) p.(Arg3484Ter) - Unknown ACMG pathogenic g.215956215G>A g.215782873G>A - - USH2A_000475 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PP1_P PubMed: Huang, X. F. et al., 2013; PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2021; PubMed: Eandi, C. M. et al., 2017 - rs111033379 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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