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     

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AscendingDNA change (cDNA)     

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+?/? 20 c.4325T>C r.(?) p.(Phe1442Ser) - Unknown - likely pathogenic g.216363636A>G g.216190294A>G - - USH2A_000856 - PubMed: de Castro-Miró 2014 - - Germline - - - - - DNA SEQ-NG-I Whole blood - retinal disease - PubMed: de Castro-Miró 2014 - M no Reunion - - - - - 1 Marta de Castro-Miró
+?/. 20 c.4325T>C r.4325T>C p.Phe1442Ser - Unknown - likely pathogenic g.216363636A>G g.216190294A>G - - USH2A_000856 - - - - Unknown ? - - - - DNA SEQ-NG-I - Gene Panel (79 IRD genes) retinal disease IRD4.0_#22 Manuscript under review (González-del Pozo et al., 2018) - ? ? Spain - - - - - 1 María González-del Pozo
+?/? 20 c.4325T>C r.(=) p.(Phe1442Ser) Fibronectin type-III 4 (1367-1462) Paternal (confirmed) ACMG VUS g.216363636A>G g.216190294A>G - - USH2A_000856 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 20 c.4325T>C r.(=) p.(Phe1442Ser) Fibronectin type-III 4 (1367-1462) Paternal (confirmed) ACMG VUS g.216363636A>G g.216190294A>G - - USH2A_000856 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative M - Spain - - - - - 1 Anne-Françoise Roux
+?/? 20 c.4325T>C r.(=) p.(Phe1442Ser) Fibronectin type-III 4 (1367-1462) Paternal (confirmed) ACMG VUS g.216363636A>G g.216190294A>G - - USH2A_000856 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 20 c.4325T>C r.(=) p.(Phe1442Ser) Fibronectin type-III 4 (1367-1462) Paternal (confirmed) ACMG VUS g.216363636A>G g.216190294A>G - - USH2A_000856 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative M - Spain - - - - - 1 Anne-Françoise Roux
+?/? 20 c.4325T>C r.(=) p.(Phe1442Ser) Fibronectin type-III 4 (1367-1462) Paternal (confirmed) ACMG VUS g.216363636A>G g.216190294A>G - - USH2A_000856 Heterozygous; pathogenic PubMed: Méndez-Vidal 2013, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - RPar - PubMed: Méndez-Vidal 2013 Relative F - Spain - - - - - 1 Anne-Françoise Roux
+?/. - c.4325T>C r.(?) p.(Phe1442Ser) - Unknown - likely pathogenic g.216363636A>G g.216190294A>G M19: c.4325T >C; p.Phe1442Ser - USH2A_000856 - PubMed: Gonzalez del Pozo 2018 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG blood solved retinal disease N (II:12) PubMed: Gonzalez del Pozo 2018 - ? no Spain - - - - - 1 LOVD
+?/. 20 c.4325T>C r.(?) p.(Phe1442Ser) - Unknown - likely pathogenic g.216363636A>G - c.4325T>C - USH2A_000856 - PubMed: de Castro-Miró-2014 - - Germline - - - - - DNA SEQ-NG - WES retinal disease E5 PubMed: de Castro-Miró-2014 - - - - - - - - - 1 LOVD
+?/. 20 c.4325T>C r.(?) p.(Phe1442Ser) - Parent #2 - likely pathogenic g.216363636A>G - c.4325T>C - USH2A_000856 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
+?/. 20 c.4325T>C r.(?) p.(Phe1442Ser) - Parent #2 - likely pathogenic g.216363636A>G - c.4325T>C - USH2A_000856 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - F - - - - - - - 1 Daan Panneman
?/. - c.4325T>C r.(?) p.(Phe1442Ser) - Unknown ACMG VUS g.216363636A>G g.216190294A>G - - USH2A_000856 ACMG GN005 criteria: PM2_P PM3_P PP3_P PubMed: Gonzalez-Del Pozo, M. et al., 2018 - rs766108245 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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