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     

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     
?/. - c.3045C>G r.(?) p.(His1015Gln) - Unknown - VUS g.216390841G>C g.216217499G>C USH2A(NM_206933.2):c.3045C>G (p.H1015Q) - USH2A_001654 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.3045C>G r.(?) p.(His1015Gln) - Parent #1 - pathogenic (recessive) g.216390841G>C g.216217499G>C - - USH2A_001654 - PubMed: Karali 2019, Journal: Karali 2019 - - Germline - - - - - DNA SEQ-NG - - retinal disease Fam25P29 PubMed: Karali 2019, Journal: Karali 2019 - - - Italy - - - - - 1 Sandro Banfi
+/. - c.3045C>G r.(?) p.(His1015Gln) - Parent #2 - pathogenic g.216390841G>C g.216217499G>C - - USH2A_001654 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 1977 PubMed: Haer-Wigman 2017 patient - no Netherlands - - - - - 1 LOVD
+/. 15 c.3045C>G r.(?) p.(His1015Gln) - Parent #1 ACMG pathogenic (recessive) g.216390841G>C - - - USH2A_001654 Parents unavailable for testing. PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-I - Exome sequencing MPS1 Pat50 PubMed: Bahena 2021 - F yes Iran - - - - - 1 Barbara Vona
+?/. 15 c.3045C>G r.(?) p.(His1015Gln) - Unknown - likely pathogenic g.216390841G>C g.216217499G>C USH2A Ex.15 c.3045C>G p.(His1015Gln), Ex.28 c.5612G>A p.(Gly1871Asp) - USH2A_001654 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA arraySNP - - retinal disease RP-2887 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
?/. - c.3045C>G r.(?) p.(His1015Gln) - Unknown ACMG VUS g.216390841G>C g.216217499G>C - - USH2A_001654 ACMG GN005 criteria: PubMed: Karali, M. et al., 2019 - rs541918040 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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