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     
+?/. - c.3745C>T r.(?) p.(Pro1249Ser) - Unknown ACMG VUS g.216373035G>A - - - USH2A_002121 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_SS_0016 - - F - Korea, South (Republic) - - - - - 1 Jinu Han
?/. - c.3745C>T r.(?) p.(Pro1249Ser) - Unknown ACMG VUS g.216373035G>A g.216199693G>A USH2A c.C3745T, p.P1249S - USH2A_002121 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 114 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
?/. - c.3745C>T r.(?) p.(Pro1249Ser) - Unknown ACMG VUS g.216373035G>A g.216199693G>A - - USH2A_002121 ACMG GN005 criteria: PM2_P PM3_P PubMed: Ma, D. J. et al., 2021 - rs751571261 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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