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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Effect     

Exon     

AscendingDNA change (cDNA)     

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DNA change (hg38)     

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-/? 42 c.8431C>A r.(?) p.(Pro2811Thr) Fibronectin type-III 14 (2724-2812) Paternal (confirmed) ACMG likely benign g.216052233G>T g.215878891G>T - - USH2A_000358 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - rs111033529 Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - Italy - - - - - 1 Anne-Françoise Roux
?/. - c.8431C>A r.(?) p.(Pro2811Thr) - Unknown - VUS g.216052233G>T g.215878891G>T USH2A(NM_206933.2):c.8431C>A (p.P2811T) - USH2A_000358 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.8431C>A r.(?) p.(Pro2811Thr) - Parent #1 - VUS g.216052233G>T g.215878891G>T - - USH2A_000358 3 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs111033529 Germline - 3/2794 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 3 Mohammed Faruq
+?/. - c.8431C>A r.(?) p.(Pro2811Thr) - Unknown - likely pathogenic (recessive) g.216052233G>T - 1:216052233G>T ENST00000307340.3:c.8431C>A (Pro2811Thr) - USH2A_000358 - PubMed: Carss 2017 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease G005241 PubMed: Carss 2017 - F - United Kingdom (Great Britain) Asia-South - - - - 1 LOVD
+/. - c.8431C>A r.(?) p.(Pro2811Thr) - Parent #2 ACMG pathogenic (recessive) g.216052233G>T g.215878891G>T - - USH2A_000358 - PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19207 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
+?/. - c.8431C>A r.(?) p.(Pro2811Thr) - Unknown - likely pathogenic g.216052233G>T g.215878891G>T - - USH2A_000358 - PubMed: Wang 2017 - rs111033529 Germline - - - - - DNA SEQ, SEQ-NG - 184-gene panel retinal disease RD14–02 PubMed: Wang 2017 - - - United States - - - - - 1 LOVD
+/. 42 c.8431C>A r.(?) p.(Pro2811Thr) - Unknown ACMG pathogenic g.216052233G>T g.215878891G>T USH2A c.8431C>A, p.(P2811T) - USH2A_000358 - PubMed: Xiao-2021 - - Unknown yes - - - - DNA SEQ-NG blood gene panel testing retinal disease 19207 PubMed: Xiao-2021 - M - China - - - - - 1 LOVD
?/. - c.8431C>A r.(?) p.(Pro2811Thr) - Unknown ACMG VUS g.216052233G>T g.215878891G>T - - USH2A_000358 ACMG GN005 criteria: PubMed: Sun, T. et al., 2018 - rs111033529 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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