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.

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/. 2 c.80C>A r.(?) p.(Ser27*) - Unknown ACMG pathogenic g.216595599G>T g.216422257G>T NM_206933.2:c.80C>A, NP_996816.2:p.(Ser27Ter), NC_000001.10:g.216595599G>T - USH2A_002149 - PubMed: Wang 2018 - - Germline ? - - - - DNA SEQ-NG - panel of 441 hereditary eye disease genes including 291 genes related to IRD retinal disease 2016041901 PubMed: Wang 2018 - F ? China Han Chinese - - - - 1 LOVD
+?/. 2 c.80C>A r.(?) p.(Ser27*) - Parent #2 ACMG likely pathogenic g.216595599G>T g.216422257G>T USH2A c.80C>A, p.Ser27* - USH2A_002149 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes USH 34 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+/. - c.80C>A r.(?) p.(Ser27Ter) - Unknown ACMG pathogenic g.216595599G>T g.216422257G>T - - USH2A_002149 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Meng, X. et al., 2021 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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