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.

12 entries on 1 page. Showing entries 1 - 12.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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Owner     
+/. 70 c.15089C>A r.(15089c>a) p.(Ser5030*) - Parent #2 - pathogenic g.215808009G>T g.215634667G>T - - USH2A_000045 - - - - Germline yes - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) USH IRD4.0_#41 Manuscript under review (González-del Pozo et al., 2018) - ? ? Spain - - - - - 1 María González-del Pozo
+/+ 70 c.15089C>A r.(?) p.(Ser5030*) - Parent #2 - pathogenic g.215808009G>T g.215634667G>T - - USH2A_000045 Heterozygous PubMed: Baux 2007 - - Germline - - -AlwI;-Sau3AI;-MboI;-BstUI;-DpnI;-BfuCI; - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband M - Italy - - - - - 1 Anne-Françoise Roux
+/+ 70 c.15089C>A r.(?) p.(Ser5030*) - Unknown - pathogenic g.215808009G>T g.215634667G>T - - USH2A_000045 Heterozygous; Pathogenic PubMed: Bonnet 2011 - - Germline - - -AlwI;-Sau3AI;-MboI;-BstUI;-DpnI;-BfuCI; - - DNA SEQ - - USH2 - PubMed: Bonnet 2011 Proband - - - - - - - - 1 Anne-Françoise Roux
+/+ 70 c.15089C>A r.(?) p.(Ser5030*) - Parent #1 - pathogenic g.215808009G>T g.215634667G>T - - USH2A_000045 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 70 c.15089C>A r.(?) p.(Ser5030*) - Parent #1 - pathogenic g.215808009G>T g.215634667G>T - - USH2A_000045 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S, PCRq, arrayCGH - - USH2 - PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/. - c.15089C>A r.(?) p.(Ser5030*) - Paternal (confirmed) - pathogenic g.215808009G>T g.215634667G>T M18: c.15089C > A; p.Ser5030* - USH2A_000045 - PubMed: Gonzalez del Pozo 2018 - - Germline yes - - - - DNA SEQ-NG blood solved retinal disease M (II:1) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
+/. - c.15089C>A r.(?) p.(Ser5030Ter) - Unknown ACMG pathogenic g.215808009G>T - - - USH2A_000045 - PubMed: Mansard et al, 2021 - rs758660532 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.15089C>A r.(?) p.(Ser5030Ter) - Unknown ACMG pathogenic g.215808009G>T - - - USH2A_000045 - PubMed: Mansard et al, 2021 - rs758660532 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+/. - c.15089C>A r.(?) p.(Ser5030Ter) - Maternal (confirmed) ACMG pathogenic g.215808009G>T - - - USH2A_000045 - PubMed: Mansard et al, 2021 - rs758660532 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - M - - - - - - - 1 Anne-Françoise Roux
+?/. 70 c.15089C>A r.(?) p.(Ser5030*) - Unknown - likely pathogenic g.215808009G>T - c.15089C>A,p.S5030X - USH2A_000045 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. 70 c.15089C>A r.(15089c>a) p.(Ser5030Ter) - Parent #1 ACMG pathogenic g.215808009G>T g.215634667G>T - - USH2A_000045 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH24 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+/. - c.15089C>A r.(?) p.(Ser5030Ter) - Unknown ACMG pathogenic g.215808009G>T g.215634667G>T - - USH2A_000045 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Bonnet, C. et al., 2016; PubMed: Gonzalez-Del Pozo, M. et al., 2018; PubMed: Mansard, L. et al., 2021 - rs758660532 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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