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.

8 entries on 1 page. Showing entries 1 - 8.
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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)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Segregation     

Frequency     

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     
+/. - c.8079G>A r.(?) p.(Trp2693Ter) - Unknown - pathogenic g.216061912C>T g.215888570C>T USH2A(NM_206933.2):c.8079G>A (p.W2693*), USH2A(NM_206933.4):c.8079G>A (p.W2693*) - USH2A_001361 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.8079G>A r.(?) p.(Trp2693Ter) - Unknown - pathogenic g.216061912C>T g.215888570C>T USH2A(NM_206933.2):c.8079G>A (p.W2693*), USH2A(NM_206933.4):c.8079G>A (p.W2693*) - USH2A_001361 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.8079G>A r.(?) p.(Trp2693Ter) - Unknown - pathogenic g.216061912C>T g.215888570C>T USH2A(NM_206933.2):c.8079G>A (p.W2693*), USH2A(NM_206933.4):c.8079G>A (p.W2693*) - USH2A_001361 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.8079G>A r.(?) p.(Trp2693Ter) - Parent #1 - pathogenic g.216061912C>T g.215888570C>T - - USH2A_001361 - PubMed: Khan 2017 - - Germline - - - - - DNA SEQ-NG - 105-gene panel retinal disease 3501 PubMed: Khan 2017 see paper - - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. 41 c.8079G>A r.(8079g>a) p.(Trp2693*) - Parent #1 ACMG pathogenic g.216061912C>T g.215888570C>T - - USH2A_001361 - Journal: Reurink 2021 - - Germline yes - - - - DNA SEQ-NG - gene panel retinal disease W02-118 Journal: Reurink 2021 - - - Netherlands - - - - - 1 Janine Reurink
+?/. - c.8079G>A r.(?) p.(Trp2693*) - Parent #1 - likely pathogenic g.216061912C>T g.215888570C>T USH2A c.8079G>A - USH2A_001361 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 16 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.8079G>A r.(?) p.(Trp2693*) - Parent #1 ACMG pathogenic g.216061912C>T g.215888570C>T USH2A c.8079G>A, p.(Trp2693*) - USH2A_001361 heterozygous PubMed: Reurink 2021 - - Germline yes - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W02-118 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.8079G>A r.(?) p.(Trp2693Ter) - Unknown ACMG pathogenic g.216061912C>T g.215888570C>T - - USH2A_001361 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Reurink, J. et al., 2021 - rs1553273330 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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