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     

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Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

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Remarks     

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VIP     

Data_av     

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Panel size     

Owner     
?/. 18 c.4021G>C r.(?) p.(Ala1341Pro) - Unknown ACMG VUS g.216198375C>G g.216198375C>G USH2A c.4021G > C, p.Ala1341Pro, heterozygous - USH2A_002305 - PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted NGS with molecular inversion probes: coding exons of 27 genes associated with Joubert syndrome retinal disease 19 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
?/. - c.4021G>C r.(?) p.(Ala1341Pro) - Parent #2 - VUS g.216371717C>G g.216198375C>G USH2A c.4021G>C, p.Ala1341Pro - USH2A_002305 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD18113666 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
?/. - c.4021G>C r.(?) p.(Ala1341Pro) - Unknown ACMG VUS g.216371717C>G g.216198375C>G - - USH2A_002305 ACMG GN005 criteria: PM2_P PM3_P PubMed: Gao, F. J. et al., 2021; PubMed: Sun, Y. et al., 2020 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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