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.

5 entries on 1 page. Showing entries 1 - 5.
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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     
+/. 46 c.9120G>A r.(?) p.(Trp3040*) - Parent #1 - pathogenic g.216017774C>T g.215844432C>T - - USH2A_000474 possible duplicate; unknown variant 2nd chromosome PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-25 (D60) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - F no Denmark - - - - - 1 Anne-Françoise Roux
+/. 13 c.9120G>A r.(?) p.(Trp3040*) - Parent #1 - pathogenic (recessive) g.216017774C>T g.215844432C>T - - USH2A_000474 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-43 (D10) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 family, 2 affeted M no Denmark - - - - - 2 Anne-Françoise Roux
+/. 13 c.9120G>A r.(?) p.(Trp3040*) - Parent #1 - pathogenic (recessive) g.216017774C>T g.215844432C>T 1920G>A - USH2A_000474 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-43a (D06) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - M no Denmark - - - - - 1 Anne-Françoise Roux
+/. 46 c.9120G>A r.(?) p.(Trp3040*) - Parent #2 - pathogenic (recessive) g.216017774C>T g.215844432C>T - - USH2A_000474 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-42 (D05) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - F no Denmark - - - - - 1 Anne-Françoise Roux
+/. 46 c.9120G>A r.(?) p.(Trp3040*) - Both (homozygous) ACMG pathogenic g.216017774C>T g.215844432C>T USH2A c.9120G>A, p.W3040* - USH2A_000474 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 42688980 PubMed: Zhu 2021 family 162, patient 42688980 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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