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     
+/. 64 c.14011G>T r.14011U>T p.Glu4671* - Parent #2 - pathogenic g.215844436C>A g.215671094C>A - - USH2A_001023 - - - - Germline yes - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) retinal disease IRD4.0_#38 Manuscript under review (González-del Pozo et al., 2018) - ? ? Spain - - - - - 1 María González-del Pozo
+?/. - c.14011G>T r.(?) p.(Glu4671*) - Maternal (confirmed) - likely pathogenic g.215844436C>A g.215671094C>A M16: c.14011G > T; p.Glu4671* - USH2A_001023 - PubMed: Gonzalez del Pozo 2018 - - Germline yes - - - - DNA SEQ-NG blood solved retinal disease K (II:1) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
+/. - c.14011G>T r.(?) p.(Glu4671Ter) - Unknown ACMG pathogenic g.215844436C>A g.215671094C>A - - USH2A_001023 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PP1_P PubMed: Gonzalez-Del Pozo, M. et al., 2018 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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