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.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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?/. - c.12910G>A r.(?) p.(Glu4304Lys) - Unknown - VUS g.215848343C>T g.215675001C>T USH2A(NM_206933.2):c.12910G>A (p.E4304K), USH2A(NM_206933.4):c.12910G>A (p.E4304K) - USH2A_000605 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/? 63 c.12910G>A r.(?) p.(Glu4304Lys) Fibronectin type-III 28 (4265-4351) Unknown ACMG likely benign g.215848343C>T g.215675001C>T - - USH2A_000605 Heterozygous; UV1 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
?/. - c.12910G>A r.(?) p.(Glu4304Lys) - Unknown - VUS g.215848343C>T g.215675001C>T USH2A(NM_206933.2):c.12910G>A (p.E4304K), USH2A(NM_206933.4):c.12910G>A (p.E4304K) - USH2A_000605 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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