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.

7 entries on 1 page. Showing entries 1 - 7.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

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Disease     

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+/+ 51 c.11065C>T r.(?) p.(Arg3689*) Fibronectin type-III 22 (3677-3767) Paternal (confirmed) - pathogenic g.215933168G>A g.215759826G>A - - USH2A_000598 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - rs41314534 Germline - - -MnlI;-TaqI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 51 c.11065C>T r.(?) p.(Arg3689*) Fibronectin type-III 22 (3677-3767) Parent #1 - pathogenic g.215933168G>A g.215759826G>A - - USH2A_000598 Heterozygous PubMed: Aparisi 2014 - rs41314534 Germline - - -MnlI;-TaqI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+/. - c.11065C>T r.(?) p.(Arg3689*) - Parent #1 - pathogenic g.215933168G>A g.215759826G>A - - USH2A_000598 - PubMed: Neuhaus 2017 - rs41314534 Germline yes - - - - DNA SEQ - - USH Pat111 PubMed: Neuhaus 2017 - - no Germany - - - - - 1 LOVD
+?/. - c.11065C>T r.(?) p.(Arg3689*) - Unknown - likely pathogenic g.215933168G>A g.215759826G>A c.76457661del p.(Met2549Alafs*3), c.11065C>T p.(Arg3689*) - USH2A_000598 - PubMed: Hagag 2020 - - Germline/De novo (untested) ? - - - - DNA ? - - retinal disease Subject 052 PubMed: Hagag 2020 - ? - - - - - - - 1 LOVD
+?/. - c.11065C>T r.(?) p.(Arg3689*) - Parent #1 - likely pathogenic g.215933168G>A g.215759826G>A USH2A c.11065C>T - USH2A_000598 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 17 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.11065C>T r.(?) p.(Arg3689Ter) - Unknown ACMG pathogenic g.215933168G>A g.215759826G>A - - USH2A_000598 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Toms, M. et al., 2020; PubMed: Aparisi, M. J. et al., 2014; PubMed: Neuhaus, C. et al., 2017 - rs41314534 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.11065C>T r.(?) p.(Arg3689Ter) - Unknown ACMG pathogenic (recessive) g.215933168G>A g.215759826G>A - - USH2A_000598 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 620107 - Germline - - - - - DNA SEQ-NG - WGS ? USHII-361 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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