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     

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Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
?/. - c.13121T>A r.(?) p.(Val4374Glu) - Parent #1 - VUS g.215848132A>T g.215674790A>T USH2A c.13121T>A, p.Val4374Glu - USH2A_002513 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH RD18040317 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+?/. 63 c.13121T>A r.(?) p.(Val4374Glu) - Parent #1 ACMG likely pathogenic g.215848132A>T g.215674790A>T USH2A c.T13121A, p.V4374E - USH2A_002513 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1645 PubMed: Zhu 2021 family 150, patient SRF_1645 F - China - - - - - 1 LOVD
?/. - c.13121T>A r.(?) p.(Val4374Glu) - Unknown ACMG VUS g.215848132A>T g.215674790A>T - - USH2A_002513 ACMG GN005 criteria: PM2_P PubMed: Gao, F. J. et al., 2021 - rs1314783581 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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