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.

8 entries on 1 page. Showing entries 1 - 8.
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-?/? 18 c.3902G>T r.(?) p.(Gly1301Val) Fibronectin type-III 3 (1242-1357) Maternal (confirmed) ACMG likely benign g.216371836C>A g.216198494C>A - - USH2A_000543 Heterozygous; Presumably pathogenic PubMed: Bonnet 2011, USMA missense analysis, missense variant in MSV3d - rs111033524 Germline - 0/484 controls none - - DNA SEQ - - USH1 - PubMed: Bonnet 2011 Proband F - - - - - - - 1 Anne-Françoise Roux
-?/? 18 c.3902G>T r.(?) p.(Gly1301Val) Fibronectin type-III 3 (1242-1357) Unknown ACMG likely benign g.216371836C>A g.216198494C>A - - USH2A_000543 Heterozygous PubMed: Lenassi 2015, USMA missense analysis, missense variant in MSV3d - rs111033524 Germline - - none - - DNA SEQ - - RPar - PubMed: Lenassi 2015 Proband - - United Kingdom (Great Britain) - - - - - 1 Eva Lenassi
-/. - c.3902G>T r.(?) p.(Gly1301Val) - Parent #1 - benign g.216371836C>A g.216198494C>A - - USH2A_000543 30 heterozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs111033524 Germline - 30/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 30 Mohammed Faruq
-/. - c.3902G>T r.(?) p.(Gly1301Val) - Both (homozygous) - benign g.216371836C>A g.216198494C>A - - USH2A_000543 1 homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs111033524 Germline - 1/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 1 Mohammed Faruq
+/. - c.3902G>T r.(?) p.(Gly1301Val) - Unknown - pathogenic (recessive) g.216371836C>A - 1:216371836C>A ENST00000307340.3:c.3902G>T (Gly1301Val) - USH2A_000543 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WES retinal disease B240013 PubMed: Carss 2017 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
?/. - c.3902G>T r.(?) p.(Gly1301Val) - Both (homozygous) - VUS g.216371836C>A g.215629014G>A - - USH2A_000543 - PubMed: Haer-Wigman 2017 - - Germline yes - - - - DNA SEQ-NG - gene panel ? 6494 PubMed: Haer-Wigman 2017 family - yes Netherlands - - - - - 1 LOVD
+?/. - c.3902G>T r.(?) p.(Gly1301Val) - Parent #1 - likely pathogenic g.216371836C>A g.216198494C>A USH2A, variant 1: c.3902G>T/p.G1301V, variant 2: c.13649T>G/p.V4550G - USH2A_000543 solved, compound heterozygous PubMed: Weisschuh 2020 - - Unknown ? - - - - DNA SEQ-NG blood RET8 targeted sequencing panel - see paper retinal disease 874 PubMed: Weisschuh 2020 Filing key number: 361, autosomal recessive retinitis pigmentosa, no patient Ids, consecutive numbers given M - Germany - - - - - 1 LOVD
-/. - c.3902G>T r.(?) p.(Gly1301Val) - Unknown ACMG benign g.216371836C>A g.216198494C>A - - USH2A_000543 ACMG GN005 criteria: PubMed: Lenassi, E. et al., 2015; PubMed: Weisschuh, N. et al., 2020 - rs111033524 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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