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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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+?/. 6 c.907C>A r.907C>A p.Arg303Ser - Unknown - likely pathogenic g.216498883G>T g.216325541G>T - - USH2A_000189 - - - - Unknown ? - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) retinal disease IRD4.0_#17 Manuscript under review (González-del Pozo et al., 2018) - ? ? Spain - - - - - 1 María González-del Pozo
+?/. 6 c.907C>A r.(907c>a) p.(Arg303Ser) - Parent #1 - likely pathogenic g.216498883G>T g.216325541G>T - - USH2A_000189 - - - - Germline yes - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) USH IRD4.0_#16 Manuscript under review (González-del Pozo et al., 2018) - ? ? Spain - - - - - 1 María González-del Pozo
+?/. 6 c.907C>A r.907C>A p.Arg303Ser - Parent #1 - likely pathogenic g.216498883G>T g.216325541G>T - - USH2A_000189 - - - - Germline yes - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) retinal disease IRD4.0_#14 Manuscript under review (González-del Pozo et al., 2018) - ? ? Spain - - - - - 1 María González-del Pozo
+?/? 6 c.907C>A r.(?) p.(Arg303Ser) Laminin N-terminal (271-517) Parent #2 ACMG VUS g.216498883G>T g.216325541G>T - - USH2A_000189 Heterozygous PubMed: Aller 2004, USMA missense analysis, missense variant in MSV3d - - Germline - 0/100 controls +HpyCH4V;-BceAI; - - DNA SEQ - - USH2 - PubMed: Aller 2004 Proband F - Spain - - - - - 1 Jose Maria Millan
+?/? 6 c.907C>A r.(?) p.(Arg303Ser) Laminin N-terminal (271-517) Paternal (confirmed) ACMG VUS g.216498883G>T g.216325541G>T - - USH2A_000189 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - 0/116 controls +HpyCH4V;-BceAI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. - c.907C>A r.(?) p.(Arg303Ser) - Parent #1 - pathogenic g.216498883G>T g.216325541G>T - - USH2A_000189 - PubMed: Zenteno 2020 - - Germline - 1/143 cases - - - DNA SEQ, SEQ-NG - 199 gene panel retinal disease 1180 PubMed: Zenteno 2020 family - - Mexico - - - - - 1 Johan den Dunnen
+?/. - c.907C>A r.(?) p.(Arg303Ser) - Unknown - likely pathogenic g.216498883G>T g.216325541G>T M20: c.907C > A; p.Arg303Ser - USH2A_000189 - PubMed: Gonzalez del Pozo 2018 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG blood solved retinal disease O (II:1) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
+?/. - c.907C>A r.(?) p.(Arg303Ser) - Maternal (inferred) - likely pathogenic g.216498883G>T g.216325541G>T M20: c.907C > A; p.Arg303Ser - USH2A_000189 - PubMed: Gonzalez del Pozo 2018 - - Germline yes - - - - DNA SEQ-NG blood solved retinal disease P (II:9) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
+?/. - c.907C>A r.(?) p.(Arg303Ser) - Paternal (inferred) - likely pathogenic g.216498883G>T g.216325541G>T M20: c.907C > A; p.Arg303Ser - USH2A_000189 - PubMed: Gonzalez del Pozo 2018 - - Germline yes - - - - DNA SEQ-NG blood solved retinal disease Q (II:4) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
+?/. - c.907C>A r.(?) p.(Arg303Ser) - Unknown ACMG likely pathogenic g.216498883G>T - - - USH2A_000189 - PubMed: Mansard et al, 2021 - rs748465849 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - ? - - - - - - - 1 Anne-Françoise Roux
+?/. - c.907C>A r.(?) p.(Arg303Ser) - Unknown ACMG likely pathogenic g.216498883G>T g.216325541G>T - - USH2A_000189 ACMG GN005 criteria: PM2_P PM3_M PP1_S PubMed: Gonzalez-Del Pozo, M. et al., 2018 - rs748465849 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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