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.

7 entries on 1 page. Showing entries 1 - 7.
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-/? 38 c.7130A>G r.(?) p.(Asn2377Ser) Fibronectin type-III 10 (2328-2432) Unknown ACMG likely benign g.216108128T>C g.215934786T>C - - USH2A_000626 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - rs111033394 Germline - 7/864 controls +AluI;+CviKI_1; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 38 c.7130A>G r.(?) p.(Asn2377Ser) Fibronectin type-III 10 (2328-2432) Unknown ACMG likely benign g.216108128T>C g.215934786T>C - - USH2A_000626 Heterozygous; Neutral PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs111033394 Germline - 7/864 controls +AluI;+CviKI_1; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/. - c.7130A>G r.(?) p.(Asn2377Ser) - Unknown - benign g.216108128T>C g.215934786T>C USH2A(NM_206933.2):c.7130A>G (p.N2377S), USH2A(NM_206933.4):c.7130A>G (p.N2377S) - USH2A_000626 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.7130A>G r.(?) p.(Asn2377Ser) - Unknown - VUS g.216108128T>C g.215934786T>C USH2A(NM_206933.2):c.7130A>G (p.N2377S), USH2A(NM_206933.4):c.7130A>G (p.N2377S) - USH2A_000626 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.7130A>G r.(?) p.(Asn2377Ser) - Unknown - likely benign g.216108128T>C g.215934786T>C USH2A(NM_206933.2):c.7130A>G (p.N2377S), USH2A(NM_206933.4):c.7130A>G (p.N2377S) - USH2A_000626 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.7130A>G r.(?) p.(Asn2377Ser) - Parent #1 - likely benign g.216108128T>C g.215934786T>C - - USH2A_000626 4 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs111033394 Germline - 4/2792 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 4 Mohammed Faruq
?/. - c.7130A>G r.(?) p.(Asn2377Ser) - Unknown - VUS g.216108128T>C g.215934786T>C - - USH2A_000626 - PubMed: Wang 2014 - rs111033394 Germline - - - - - DNA SEQ-NG - 66-gene panel retinal disease 38 PubMed: Wang 2014 - M - United States - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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