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     

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DNA change (hg38)     

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Owner     
+?/? 26 c.5168G>A r.(?) p.(Gly1723Glu) Laminin G-like 2 (1714-1891) Maternal (confirmed) ACMG VUS g.216256928C>T g.216083586C>T - - USH2A_000718 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - -NlaIV - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/. - c.5168G>A r.(?) p.(Gly1723Glu) - Unknown - likely pathogenic g.216256928C>T g.216083586C>T USH2A c.5168G>A, p.G1723E - USH2A_000718 heterozygous PubMed: Ng 2019 - - Germline yes - - - - DNA SEQ-NG-I blood Whole exome sequencing USH F3-II-6 PubMed: Ng 2019 proband; pedigree patient numbers differ from table numbers F - China - - - - - 1 LOVD
+/. 26 c.5168G>A r.[4988_5298del,5168_5298del] p.[Glu1663Aspfs*31,Gly1723Aspfs*31] - Unknown ACMG pathogenic g.216256928C>T - - - USH2A_000718 mini-gene splicing assay; changes ACMG to pathogenic PubMed: Reurink 2022, Journal: Reurink 2022 - - In vitro (cloned) - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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