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.

10 entries on 1 page. Showing entries 1 - 10.
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Effect     

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AscendingDNA change (cDNA)     

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+/? 17 c.3368A>G r.(?) p.(Tyr1123Cys) - Paternal (inferred) - pathogenic g.216373412T>C g.216200070T>C - - USH2A_000285 not in 114 hearing controls PubMed: Behar 2014, Journal: Behar 2014 - - Germline yes - - - - DNA SEQ-NG-I blood - USH2A - PubMed: Behar 2014, Journal: Behar 2014 3-generation family, 2 affecteds (F, M), unaffected carrier parents/sibs; family segregates GJB2 and USH2A variants F;M no Israel Iraq;Jewish;Jewish-Ashkenazi - - - - 3 Zippi Brownstein
+?/? 17 c.3368A>G r.(?) p.(Tyr1123Cys) Fibronectin type-III 1 (1058-1143) Parent #2 ACMG VUS g.216373412T>C g.216200070T>C - - USH2A_000285 Heterozygous PubMed: Le Guédard-Méreuze 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA minigene, SEQ - - USH2 - PubMed: Le Guédard-Méreuze 2010 Proband F - France - - - - - 1 Anne-Françoise Roux
+?/? 17 c.3368A>G r.(?) p.(Tyr1123Cys) Fibronectin type-III 1 (1058-1143) Parent #2 ACMG VUS g.216373412T>C g.216200070T>C - - USH2A_000285 Heterozygous USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA SEQ - - USH2 - - Relative F - France - - - - - 1 Anne-Françoise Roux
+?/? 17 c.3368A>G r.(?) p.(Tyr1123Cys) Fibronectin type-III 1 (1058-1143) Unknown ACMG VUS g.216373412T>C g.216200070T>C - - USH2A_000285 Heterozygous; Mutation PubMed: Vozzi 2011, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA PE, SEQ - APEX USH2 - PubMed: Vozzi 2011 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+?/? 17 c.3368A>G r.(?) p.(Tyr1123Cys) Fibronectin type-III 1 (1058-1143) Unknown ACMG VUS g.216373412T>C g.216200070T>C - - USH2A_000285 Heterozygous; Mutation PubMed: Vozzi 2011, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA PE, SEQ - APEX USH2 - PubMed: Vozzi 2011 Proband - - Italy - - - - - 1 Anne-Françoise Roux
?/. - c.3368A>G r.(?) p.(Tyr1123Cys) - Unknown - VUS g.216373412T>C - - - USH2A_000285 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.3368A>G r.(?) p.(Tyr1123Cys) - Parent #1 - likely pathogenic g.216373412T>C g.216200070T>C USH2A c.3368A>G, p.Y1123C - USH2A_000285 compound heterozygous PubMed: Jauregui 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted sequencing retinal disease 125 PubMed: Jauregui 2020 - F - (United States) white - - - - 1 LOVD
+?/. 17 c.3368A>G r.(?) p.(Tyr1123Cys) - Unknown - likely pathogenic g.216373412T>C - c.3368A>G - USH2A_000285 - PubMed: Colombo-2020 - rs775177930 Germline - - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+?/. 17 c.3368A>G r.(?) p.(Tyr1123Cys) - Parent #2 - likely pathogenic g.216373412T>C - c.3368A>G - USH2A_000285 - PubMed: Panneman 2023 - - Unknown - - - - - DNA SEQ - RP-LCA smMIPs sequencing RP - PubMed: Panneman 2023 - M - - - - - - - 1 Daan Panneman
?/. - c.3368A>G r.(?) p.(Tyr1123Cys) - Unknown ACMG VUS g.216373412T>C g.216200070T>C - - USH2A_000285 ACMG GN005 criteria: PM2_P PM3_P PubMed: Ganapathi, M. et al., 2022; PubMed: Colombo, L. et al., 2021; PubMed: Jauregui, R. et al., 2020 - rs775177930 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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