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.

2 entries on 1 page. Showing entries 1 - 2.
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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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Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Owner     
?/. - c.6485A>T r.(?) p.(Gln2162Leu) - Unknown ACMG VUS g.216173745T>A g.216000403T>A USH2A c.A6485T, p.Q2162L - USH2A_002416 marked as causative, heterozygous PubMed: Ma 2021 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ - whole exome sequencing retinal disease 73 PubMed: Ma 2021 - ? - Korea - - - - - 1 LOVD
?/. - c.6485A>T r.(?) p.(Gln2162Leu) - Unknown ACMG VUS g.216173745T>A g.216000403T>A - - USH2A_002416 ACMG GN005 criteria: PM2_P PM3_P PubMed: Ma, D. J. et al., 2021 - rs760264555 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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