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.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Re-site     

VIP     

Methylation     

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Technique     

Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Owner     
+/. - c.997T>C r.(?) p.(Ser333Pro) - Parent #1 - pathogenic (recessive) g.216498793A>G g.216325451A>G - - USH2A_002071 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP331 PubMed: Xu 2014 patient M - China - - - - - 1 LOVD
+?/. 6 c.997T>C r.(?) p.(Ser333Pro) - Unknown - likely pathogenic (recessive) g.216498793A>G - c.997T>C - USH2A_002071 - PubMed: Liu-2020 - - Germline - - - - - DNA SEQ-NG - hereditary eye disease enrichment panel (HEDEP) retinal disease - PubMed: Liu-2020 - M - - - - - - - 1 LOVD
+?/. 6 c.997T>C r.(?) p.(Ser333Pro) - Parent #1 ACMG likely pathogenic g.216498793A>G g.216325451A>G USH2A c.997T>C, p.S333P - USH2A_002071 single heterozygous variant in a recessive disesase, no second allele PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease 18967896 PubMed: Zhu 2021 family 223, patient 18967896 - - China - - - - - 1 LOVD
?/. - c.997T>C r.(?) p.(Ser333Pro) - Unknown ACMG VUS g.216498793A>G g.216325451A>G - - USH2A_002071 ACMG GN005 criteria: PM2_P PubMed: Kuang, L. et al., 2020 - rs368986242 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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