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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

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Owner     
-?/. - c.9262G>A r.(?) p.(Glu3088Lys) - Unknown - likely benign g.216011442C>T g.215838100C>T USH2A(NM_206933.2):c.9262G>A (p.E3088K), USH2A(NM_206933.4):c.9262G>A (p.E3088K) - USH2A_000123 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/? 47 c.9262G>A r.(?) p.(Glu3088Lys) Fibronectin type-III 17 (3020-3105) Unknown ACMG likely benign g.216011442C>T g.215838100C>T - - USH2A_000123 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 4/844 controls +MseI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/? 47 c.9262G>A r.(?) p.(Glu3088Lys) Fibronectin type-III 17 (3020-3105) Parent #2 ACMG likely benign g.216011442C>T g.215838100C>T - - USH2A_000123 Heterozygous PubMed: Baux 2007, USMA missense analysis, missense variant in MSV3d - - Germline - - +MseI - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband F - France - - - - - 1 Anne-Françoise Roux
-?/? 47 c.9262G>A r.(?) p.(Glu3088Lys) Fibronectin type-III 17 (3020-3105) Unknown ACMG likely benign g.216011442C>T g.215838100C>T - - USH2A_000123 Heterozygous; unknown PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - +MseI - - DNA SEQ - - USH2 - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 2 Anne-Françoise Roux
-?/? 47 c.9262G>A r.(?) p.(Glu3088Lys) Fibronectin type-III 17 (3020-3105) Unknown ACMG likely benign g.216011442C>T g.215838100C>T - - USH2A_000123 Heterozygous; unknown PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - +MseI - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-/- 47 c.9262G>A r.(?) p.(Glu3088Lys) Fibronectin type-III 17 (3020-3105) Unknown ACMG likely benign g.216011442C>T g.215838100C>T - - USH2A_000123 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +MseI - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-?/? 47 c.9262G>A r.(?) p.(Glu3088Lys) Fibronectin type-III 17 (3020-3105) Unknown ACMG likely benign g.216011442C>T g.215838100C>T - - USH2A_000123 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +MseI - - DNA MLPA, SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/. - c.9262G>A r.(?) p.(Glu3088Lys) - Unknown - benign g.216011442C>T g.215838100C>T USH2A(NM_206933.2):c.9262G>A (p.E3088K), USH2A(NM_206933.4):c.9262G>A (p.E3088K) - USH2A_000123 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.9262G>A r.(?) p.(Glu3088Lys) - Parent #1 - likely benign g.216011442C>T g.215838100C>T - - USH2A_000123 13 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs56056328 Germline - 13/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 13 Mohammed Faruq
?/. - c.9262G>A r.(?) p.(Glu3088Lys) - Unknown - VUS g.216011442C>T g.215838100C>T - - USH2A_000123 - PubMed: Wang 2014 - rs56056328 Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 19 PubMed: Wang 2014 - M - United States - - - - - 1 LOVD
?/. - c.9262G>A r.(?) p.(Glu3088Lys) - Unknown - VUS g.216011442C>T g.215838100C>T - - USH2A_000123 - PubMed: Wang 2014 - rs56056328 Germline - - - - - DNA SEQ-NG, PCR, SEQ - - retinal disease 32 PubMed: Wang 2014 - F ? United States - - - - - 1 Muhammad Ajmal
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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