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.

9 entries on 1 page. Showing entries 1 - 9.
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AscendingDNA change (cDNA)     

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+?/? 65 c.14287G>A r.(?) p.(Gly4763Arg) Fibronectin type-III 33 (4732-4825) Unknown ACMG VUS g.215823990C>T g.215650648C>T - - USH2A_000444 Heterozygous; likely deleterious PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
+?/? 65 c.14287G>A r.(?) p.(Gly4763Arg) Fibronectin type-III 33 (4732-4825) Unknown ACMG VUS g.215823990C>T g.215650648C>T - - USH2A_000444 Heterozygous; likely deleterious PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
+?/? 65 c.14287G>A r.(?) p.(Gly4763Arg) Fibronectin type-III 33 (4732-4825) Unknown ACMG VUS g.215823990C>T g.215650648C>T - - USH2A_000444 Heterozygous PubMed: Lenassi 2015, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenassi 2015 Proband - - Canada - - - - - 1 Eva Lenassi
+?/? 65 c.14287G>A r.(?) p.(Gly4763Arg) Fibronectin type-III 33 (4732-4825) Unknown ACMG VUS g.215823990C>T g.215650648C>T - - USH2A_000444 Heterozygous PubMed: Lenassi 2015, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Lenassi 2015 Relative - - Canada - - - - - 1 Eva Lenassi
+?/? 65 c.14287G>A r.(?) p.(Gly4763Arg) Fibronectin type-III 33 (4732-4825) Parent #2 ACMG VUS g.215823990C>T g.215650648C>T - - USH2A_000444 Heterozygous; likely deleterious PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - Slovenia - - - - - 1 Crystel Bonnet
+?/. - c.14287G>A r.(?) p.(Gly4763Arg) - Unknown ACMG VUS g.215823990C>T - - - USH2A_000444 - - - - Germline/De novo (untested) - - - - - DNA SEQ-NG-I - - RP IR_GH_0108 - - M - Korea, South (Republic) - - - - - 1 Jinu Han
+?/. - c.14287G>A r.(?) p.(Gly4763Arg) - Unknown ACMG likely pathogenic g.215823990C>T g.215650648C>T USH2A c.13045_13046insG(;)14287G>A, V2: c.14287G>A, (p.Gly4763Arg) - USH2A_000444 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F084 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+?/. - c.14287G>A r.(?) p.(Gly4763Arg) - Unknown - likely pathogenic g.215823990C>T g.215650648C>T USH2A c.13045_13046insG(;)14287G>A; p.(Gly4763Arg) - USH2A_000444 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0; GnomAD_exome_East: N.A.; GnomAD_All: N.A. - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F084 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
+/. - c.14287G>A r.(?) p.(Gly4763Arg) - Unknown ACMG pathogenic g.215823990C>T g.215650648C>T - - USH2A_000444 ACMG GN005 criteria: PS1_S PM2_P PM3_S PubMed: Lenassi, E. et al., 2015; PubMed: Bonnet, C. et al., 2016; PubMed: Kim, Y. N. et al., 2021 - rs397517990 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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