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     

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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     

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Disease     

ID_report     

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Data_av     

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Panel size     

Owner     
?/. 53 c.10505T>A r.(?) p.(Val3502Glu) - Parent #1 ACMG VUS g.215956160A>T g.215782818A>T USH2A c.10505T>A, p.Val3502Glu - USH2A_002536 heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 42 PubMed: Meng 2020 - M - China - - - - - 1 LOVD
+?/. 53 c.10505T>A r.(?) p.(Val3502Glu) - Parent #1 ACMG likely pathogenic g.215956160A>T g.215782818A>T USH2A c.10505T>A, p.V3502E - USH2A_002536 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease MEM1015 PubMed: Zhu 2021 family 46, patient MEM1015 M - China - - - - - 1 LOVD
?/. - c.10505T>A r.(?) p.(Val3502Glu) - Unknown ACMG VUS g.215956160A>T g.215782818A>T - - USH2A_002536 ACMG GN005 criteria: PM2_P PM3_P PubMed: Meng, X. et al., 2021 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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