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.

12 entries on 1 page. Showing entries 1 - 12.
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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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Template     

Technique     

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Disease     

ID_report     

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Owner     
+/. - c.2023C>T r.(?) p.(Gln675Ter) - Unknown - pathogenic g.216424389G>A g.216251047G>A - - USH2A_000024 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/+ 12 c.2023C>T r.(?) p.(Gln675*) Laminin EGF-like 3 (641-693) Unknown - pathogenic g.216424389G>A g.216251047G>A - - USH2A_000024 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls +Tsp509I;-TspRI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 12 c.2023C>T r.(?) p.(Gln675*) Laminin EGF-like 3 (641-693) Paternal (inferred) - pathogenic g.216424389G>A g.216251047G>A - - USH2A_000024 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 0/878 controls +Tsp509I;-TspRI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 12 c.2023C>T r.(?) p.(Gln675*) Laminin EGF-like 3 (641-693) Unknown - pathogenic g.216424389G>A g.216251047G>A - - USH2A_000024 Heterozygous PubMed: Dreyer 2000 - - Germline - - +Tsp509I;-TspRI; - - DNA SEQ - - USH2 - PubMed: Dreyer 2000 Proband - - Denmark - - - - - 1 Anne-Françoise Roux
+/. - c.2023C>T r.(?) p.(Gln675*) - Parent #1 ACMG pathogenic (recessive) g.216424389G>A g.216251047G>A - - USH2A_000024 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19999 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
+/. 12 c.2023C>T r.(?) p.(Gln675*) - Parent #1 - pathogenic (recessive) g.216424389G>A g.216251047G>A 2023C>T;2797C>T - USH2A_000024 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-13 (D21) PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 family, 2 affeted F no Denmark - - - - - 2 Anne-Françoise Roux
+/. 12 c.2023C>T r.(?) p.(Gln675*) - Parent #1 - pathogenic (recessive) g.216424389G>A g.216251047G>A 2023C>T;2797C>T - USH2A_000024 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-13a PubMed: Dreyer 2000, PubMed: Dreyer 2008, Tranebjaerg 2011, PubMed: Dad 2016 - M no Denmark - - - - - 1 Anne-Françoise Roux
+/. 12 c.2023C>T r.(?) p.(Gln675*) - Both (homozygous) - pathogenic (recessive) g.216424389G>A g.216251047G>A - - USH2A_000024 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA PE - - retinal disease USH2-65 PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - F no Denmark - - - - - 1 Anne-Françoise Roux
+?/. - c.2023C>T r.(?) p.(Gln675*) - Unknown - likely pathogenic g.216424389G>A g.216251047G>A c.2023C>T p.(Gln675*), c.2299delG p.(Glu767Serfs*21) - USH2A_000024 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 029 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+?/. - c.2023C>T r.(?) p.(Gln675*) - Parent #1 - likely pathogenic g.216424389G>A g.216251047G>A USH2A c.2023C>T - USH2A_000024 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 15 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. 12 c.2023C>T r.(?) p.(Gln675*) - Parent #2 ACMG pathogenic g.216424389G>A g.216251047G>A USH2A c.2023C>T, p.Q675* - USH2A_000024 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF421 PubMed: Zhu 2021 family 115, patient SRF421 M - China - - - - - 1 LOVD
+/. - c.2023C>T r.(?) p.(Gln675Ter) - Unknown ACMG pathogenic g.216424389G>A g.216251047G>A - - USH2A_000024 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Sun, T. et al., 2018; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Toms, M. et al., 2020 - rs868562952 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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