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.

4 entries on 1 page. Showing entries 1 - 4.
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AscendingDNA change (cDNA)     

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?/. - c.10510C>G r.(?) p.(Pro3504Ala) - Unknown - VUS g.215956155G>C g.215782813G>C USH2A(NM_206933.2):c.10510C>G (p.P3504A), USH2A(NM_206933.4):c.10510C>G (p.P3504A) - USH2A_000635 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 53 c.10510C>G r.(?) p.(Pro3504Ala) Fibronectin type-III 20 (3499-3585) Unknown ACMG likely benign g.215956155G>C g.215782813G>C - - USH2A_000635 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 1/842 controls +BaeGI;+Bsp1286I;-BsmFI;-MlyI;-PleI;-HinfI; - - DNA SEQ - - USH - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/. - c.10510C>G r.(?) p.(Pro3504Ala) - Unknown - benign g.215956155G>C g.215782813G>C USH2A(NM_206933.2):c.10510C>G (p.P3504A), USH2A(NM_206933.4):c.10510C>G (p.P3504A) - USH2A_000635 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.10510C>G r.(?) p.(Pro3504Ala) - Parent #1 - pathogenic (recessive) g.215956155G>C g.215782813G>C - - USH2A_000635 - PubMed: Van Huet 2015 - - Germline - - - - - DNA PE, SEQ - APEX retinal disease - PubMed: Van Huet 2015 - - - Netherlands - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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