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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (hg38)     

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?/. - c.8575C>T r.(?) p.(Arg2859Cys) - Unknown - VUS g.216051206G>A g.215877864G>A USH2A(NM_206933.4):c.8575C>T (p.R2859C) - USH2A_000755 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 43 c.8575C>T r.(=) p.(Arg2859Cys) Fibronectin type-III 15 (2821-2920) Unknown ACMG likely benign g.216051206G>A g.215877864G>A - - USH2A_000755 Heterozygous PubMed: Besnard, Garcia-Garcia 2014, USMA missense analysis, missense variant in MSV3d - rs138087806 Germline - - -BsmAI;-BsmBI;-HpyCH4IV; - - DNA SEQ, SEQ-NG-S - - DFN - PubMed: Besnard, Garcia-Garcia 2014 Proband M - Spain - - - - - 1 Anne-Françoise Roux
?/. - c.8575C>T r.(?) p.(Arg2859Cys) - Unknown - VUS g.216051206G>A g.215877864G>A USH2A(NM_206933.4):c.8575C>T (p.R2859C) - USH2A_000755 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.8575C>T r.(?) p.(Arg2859Cys) - Parent #1 - VUS g.216051206G>A g.215877864G>A USH2A c.8575C>T, p.Arg2859Cys - USH2A_000755 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing retinal disease RD17050721 PubMed: Gao 2021 - F - China - - - - - 1 LOVD
-?/. - c.8575C>T r.(?) p.(Arg2859Cys) - Unknown ACMG likely benign g.216051206G>A g.215877864G>A - - USH2A_000755 ACMG GN005 criteria: BS2_S BP4_P PubMed: Gao, F. J. et al., 2021 - rs138087806 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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