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)     

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DNA change (hg38)     

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+/. 18 c.3932C>A r.(?) p.(Ser1311*) Fibronectin type-III 3 (1242-1357) Parent #2 - pathogenic (recessive) g.216371806G>T - - - USH2A_000470 - PubMed: Ivanova 2018 - rs79279902 Germline - - - - - DNA SEQ-NG-S - - USH2 Pat12 PubMed: Ivanova 2018 Proband M - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+/. - c.3932C>A r.(?) p.(Ser1311Ter) - Unknown ACMG pathogenic g.216371806G>T - - - USH2A_000470 - PubMed: Mansard et al, 2021 - rs79279902 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+/. 18 c.3932C>A r.(?) p.(Ser1311*) - Unknown - pathogenic g.216371806G>T - c.3932C>A - USH2A_000470 - PubMed: Colombo-2020 - rs79279902 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. - c.3932C>A r.(?) p.(Ser1311Ter) - Unknown ACMG pathogenic g.216371806G>T g.216198464G>T - - USH2A_000470 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Colombo, L. et al., 2022; PubMed: Mansard, L. et al., 2021; PubMed: Colombo, L. et al., 2021 - rs79279902 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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