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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 13 c.2797C>T r.(?) p.(Gln933*) Laminin EGF-like 8 (900-950) Parent #2 - pathogenic g.216419939G>A g.216246597G>A - - USH2A_000015 Heterozygous PubMed: Dreyer 2000 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Dreyer 2000 Proband - - Denmark - - - - - 1 Anne-Françoise Roux
+/+ 13 c.2797C>T r.(?) p.(Gln933*) Laminin EGF-like 8 (900-950) Unknown - pathogenic g.216419939G>A g.216246597G>A - - USH2A_000015 Heterozygous PubMed: Dreyer 2000 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Dreyer 2000 Proband - - Denmark - - - - - 1 Anne-Françoise Roux
+/+ 13 c.2797C>T r.(?) p.(Gln933*) Laminin EGF-like 8 (900-950) Unknown - pathogenic g.216419939G>A g.216246597G>A - - USH2A_000015 Heterozygous; mutation PubMed: Krawitz 2014 - - Germline - - - - - DNA SEQ-NG-S - - USH2 - PubMed: Krawitz 2014 Proband M - Germany - - - - - 1 Peter Krawitz
+/. - c.2797C>T r.(?) - - Parent #1 - pathogenic (recessive) g.216419939G>A g.216246597G>A 2023C>T;2797C>T - USH2A_000015 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
+/. - c.2797C>T r.(?) - - Parent #1 - pathogenic (recessive) g.216419939G>A g.216246597G>A 2023C>T;2797C>T - USH2A_000015 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
+/. 13 c.2797C>T r.(?) p.(Gln933*) - Parent #2 - pathogenic (recessive) g.216419939G>A g.216246597G>A - - USH2A_000015 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-36 (D07) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - F no Denmark - - - - - 1 Anne-Françoise Roux
+/. 13 c.2797C>T r.(?) p.(Gln933*) - Parent #1 ACMG pathogenic g.216419939G>A g.216246597G>A USH2A c.2797C>T, p.Q933* - USH2A_000015 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 44111577 PubMed: Zhu 2021 family 2, patient 44111577 F - China - - - - - 1 LOVD
+/. 13 c.2797C>T r.(?) p.(Gln933*) - Parent #1 ACMG pathogenic g.216419939G>A g.216246597G>A USH2A c.2797C>T, p.Q933* - USH2A_000015 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 44111577_1 PubMed: Zhu 2021 family 2, patient 44111577_1 M - China - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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