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.

2 entries on 1 page. Showing entries 1 - 2.
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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.12569T>C r.(?) p.(Val4190Ala) - Unknown - pathogenic g.215848684A>G g.215675342A>G - - USH2A_001970 - PubMed: Bravo-Gil 2016 - - Germline - - - - - DNA SEQ-NG - 64-gene panel retinal disease 435 PubMed: Bravo-Gil 2016 see paper - - Spain - - - - - 1 LOVD
?/. - c.12569T>C r.(?) p.(Val4190Ala) - Unknown ACMG VUS g.215848684A>G g.215675342A>G - - USH2A_001970 ACMG GN005 criteria: PM2_P PM3_M PP1_P PubMed: Bravo-Gil, N. et al., 2016 - rs979037444 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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