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     

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VIP     

Data_av     

Treatment     

Panel size     

Owner     
+/+ 34 c.6488G>A r.(?) p.(Trp2163*) Fibronectin type-III 8 (2142-2236) Parent #1 - pathogenic g.216172398C>T g.215999056C>T - - USH2A_000968 Heterozygous; mutation PubMed: Jiang 2015 - rs763389877 Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Jiang 2015 Proband F - China - - - - - 1 Anne-Françoise Roux
+/. 34 c.6488G>A r.(?) p.(Trp2163*) - Parent #1 ACMG pathogenic g.216172398C>T g.215999056C>T USH2A c.6488G>A, p.W2163* - USH2A_000968 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease USHsrf35 PubMed: Zhu 2021 family 204, patient USHsrf35 F - China - - - - - 1 LOVD
+?/. - c.6488G>A r.(?) p.(Trp2163Ter) - Unknown ACMG likely pathogenic g.216172398C>T g.215999056C>T - - USH2A_000968 ACMG GN005 criteria: PVS1_VS PM2_P PubMed: Jiang, L. et al., 2015 - rs763389877 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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