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     

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DNA change (hg38)     

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ISCN     

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-?/. - c.11597C>T r.(?) p.(Ala3866Val) - Unknown - likely benign g.215914831G>A g.215741489G>A USH2A(NM_206933.2):c.11597C>T (p.A3866V) - USH2A_000561 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 60 c.11597C>T r.(?) p.(Ala3866Val) Fibronectin type-III 24 (3863-3960) Paternal (inferred) ACMG likely benign g.215914831G>A g.215741489G>A - - USH2A_000561 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/878 controls +BsmFI;-Fnu4HI;-ApeKI;-BbvI;-TseI;-CviKI_1; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
?/. - c.11597C>T r.(?) p.(Ala3866Val) - Unknown - VUS g.215914831G>A g.215741489G>A USH2A(NM_206933.2):c.11597C>T (p.A3866V) - USH2A_000561 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. 60 c.11597C>T r.(11597c>u) p.(Ala3866Val) - Parent #1 ACMG likely benign g.215914831G>A g.215741489G>A - - USH2A_000561 no variant 2nd chromome PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP44 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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