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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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

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Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
-/? 55 c.10836C>A r.(?) p.(=) Fibronectin type-III 21 (3590-3676) Unknown ACMG likely benign g.215953288G>T g.215779946G>T - - USH2A_000459 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs61276761 Germline - 1/830 controls +Hpy166II;+CviQI;+RsaI;-BsmFI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? 55 c.10836C>A r.(?) p.(=) Fibronectin type-III 21 (3590-3676) Unknown ACMG likely benign g.215953288G>T g.215779946G>T - - USH2A_000459 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs61276761 Germline - 1/830 controls +Hpy166II;+CviQI;+RsaI;-BsmFI - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/? 55 c.10836C>A r.(?) p.(=) Fibronectin type-III 21 (3590-3676) Unknown ACMG likely benign g.215953288G>T g.215779946G>T - - USH2A_000459 Heterozygous; polymorphism PubMed: McGee 2010 - rs61276761 Germline - - +Hpy166II;+CviQI;+RsaI;-BsmFI - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-/? 55 c.10836C>A r.(?) p.(=) Fibronectin type-III 21 (3590-3676) Paternal (inferred) ACMG likely benign g.215953288G>T g.215779946G>T - - USH2A_000459 Homozygous; polymorphism PubMed: Baux 2014 - rs61276761 Germline - - +Hpy166II;+CviQI;+RsaI;-BsmFI - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Baux 2014 Proband M - Haiti - - - - - 1 Anne-Françoise Roux
-/? 55 c.10836C>A r.(?) p.(=) Fibronectin type-III 21 (3590-3676) Maternal (inferred) ACMG likely benign g.215953288G>T g.215779946G>T - - USH2A_000459 Homozygous; polymorphism PubMed: Baux 2014 - rs61276761 Germline - - +Hpy166II;+CviQI;+RsaI;-BsmFI - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Baux 2014 Proband M - Haiti - - - - - 1 Anne-Françoise Roux
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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