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.

10 entries on 1 page. Showing entries 1 - 10.
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-/. - c.15076A>G r.(?) p.(Lys5026Glu) - Unknown - benign g.215808022T>C g.215634680T>C USH2A(NM_206933.2):c.15076A>G (p.K5026E) - USH2A_000280 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 70 c.15076A>G r.(?) p.(Lys5026Glu) - Unknown - benign g.215808022T>C g.215634680T>C - - USH2A_000280 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs41308435 Germline - 16/876 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 70 c.15076A>G r.(?) p.(Lys5026Glu) - Paternal (inferred) - benign g.215808022T>C g.215634680T>C - - USH2A_000280 Homozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs41308435 Germline - 16/876 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 70 c.15076A>G r.(?) p.(Lys5026Glu) - Maternal (inferred) - benign g.215808022T>C g.215634680T>C - - USH2A_000280 Homozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs41308435 Germline - 16/876 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 70 c.15076A>G r.(?) p.(Lys5026Glu) - Unknown - benign g.215808022T>C g.215634680T>C - - USH2A_000280 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs41308435 Germline - 16/876 controls none - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 70 c.15076A>G r.(?) p.(Lys5026Glu) - Paternal (confirmed) - benign g.215808022T>C g.215634680T>C - - USH2A_000280 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs41308435 Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - Italy - - - - - 1 Anne-Françoise Roux
-/- 70 c.15076A>G r.(?) p.(Lys5026Glu) - Unknown - benign g.215808022T>C g.215634680T>C - - USH2A_000280 Heterozygous; benign PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - rs41308435 Germline - - - - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 2 Anne-Françoise Roux
-/. - c.15076A>G r.(?) p.(Lys5026Glu) - Unknown - benign g.215808022T>C g.215634680T>C - - USH2A_000280 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs41308435 Germline - 185/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 185 Yoshito Koyanagi
-/. - c.15076A>G r.(?) p.(Lys5026Glu) - Both (homozygous) - benign g.215808022T>C g.215634680T>C - - USH2A_000280 - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 - rs41308435 Germline - 13/1204 cases with retinitis pigmentosa - - - DNA SEQ-NG - - retinal disease - PubMed: Koyanagi 2019, Journal: Koyanagi 2019 analysis 1204 retinitis pigmentosa cases - - Japan - - - - - 13 Yoshito Koyanagi
-/. - c.15076A>G r.(?) p.(Lys5026Glu) - Unknown - benign g.215808022T>C g.215634680T>C USH2A(NM_206933.2):c.15076A>G (p.K5026E) - USH2A_000280 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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