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.

5 entries on 1 page. Showing entries 1 - 5.
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AscendingDNA change (cDNA)     

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+?/? 19 c.4133T>C r.(?) p.(Leu1378Pro) Fibronectin type-III 4 (1367-1462) Paternal (confirmed) ACMG VUS g.216370013A>G g.216196671A>G - - USH2A_000637 Heterozygous; UV4 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/878 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/? 19 c.4133T>C r.(?) p.(Leu1378Pro) Fibronectin type-III 4 (1367-1462) Maternal (confirmed) ACMG VUS g.216370013A>G g.216196671A>G - - USH2A_000637 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - none - - DNA arrayCGH, SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
?/. - c.4133T>C r.(?) p.(Leu1378Pro) - Parent #1 - VUS g.216370013A>G g.216196671A>G - - USH2A_000637 - PubMed: Comander 2017 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease Pat16 PubMed: Comander 2017 proband, affected brother M - United States - - - - - 1 Johan den Dunnen
?/. 19 c.4133T>C r.(4133u>c) p.(Leu1378Pro) - Parent #2 ACMG VUS g.216370013A>G g.216196671A>G - - USH2A_000637 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH29 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
?/. - c.4133T>C r.(?) p.(Leu1378Pro) - Unknown ACMG VUS g.216370013A>G g.216196671A>G - - USH2A_000637 ACMG GN005 criteria: PM2_P PM3_P PubMed: Le Quesne Stabej, P. et al., 2012 - rs2034852728 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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