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.14285A>G r.(?) p.(Asn4762Ser) - Unknown - likely pathogenic g.215823992T>C g.215650650T>C - - USH2A_000580 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/? 65 c.14285A>G r.(?) p.(Asn4762Ser) Fibronectin type-III 33 (4732-4825) Unknown ACMG VUS g.215823992T>C g.215650650T>C - - USH2A_000580 Heterozygous; UV3 PubMed: Le Quesne Stabej 2012, USMA missense analysis, missense variant in MSV3d - - Germline - 0/878 controls +BseYI;+MspA1I;+AciI;+FauI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+?/. - c.14285A>G r.(?) p.(Asn4762Ser) - Unknown - likely pathogenic g.215823992T>C g.215650650T>C - - USH2A_000580 - PubMed: Huang 2018 - - Germline - - - - - DNA SEQ-NG - 283-gene panel retinal disease RP063 PubMed: Huang 2018 - - - - - - - - - 1 LOVD
+/. - c.14285A>G r.(?) p.(Asn4762Ser) - Parent #2 - pathogenic (recessive) g.215823992T>C g.215650650T>C - - USH2A_000580 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP315 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
+/. 65 c.14285A>G r.(?) p.(Asn4762Ser) - Both (homozygous) ACMG pathogenic g.215650650T>C g.215650650T>C USH2A c.14285A > G, p.Asn4762Ser, homozygous - USH2A_000580 - PubMed: Sun 2020 - - Unknown ? - - - - DNA SEQ-NG blood targeted NGS with molecular inversion probes: coding exons of 27 genes associated with Joubert syndrome retinal disease 15 PubMed: Sun 2020 - M - China - - - - - 1 LOVD
+?/. 65 c.14285A>G r.(?) p.(Asn4762Ser) - Parent #2 ACMG likely pathogenic g.215823992T>C g.215650650T>C USH2A c.14285A>G, - USH2A_000580 error in annotation, protein change not originally in the table, only coding DNA given; heterozygous PubMed: Meng 2020 - - Unknown ? - - - - DNA SEQ-NG-I blood hereditary eye disease enrichment panel (HEDEP) - 441 genes covering 14 Usher genes retinal disease 65 PubMed: Meng 2020 - F - China - - - - - 1 LOVD
+?/. - c.14285A>G r.(?) p.(Asn4762Ser) - Parent #2 - likely pathogenic g.215823992T>C g.215650650T>C USH2A c.14285A>G - USH2A_000580 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 20 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. 65 c.14285A>G r.(?) p.(Asn4762Ser) - Parent #2 ACMG likely pathogenic g.215823992T>C g.215650650T>C USH2A c.14285A>G, p.N4762S - USH2A_000580 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_8 PubMed: Zhu 2021 family 28, patient AXLM_8 F - China - - - - - 1 LOVD
+?/. 65 c.14285A>G r.(?) p.(Asn4762Ser) - Parent #2 ACMG likely pathogenic g.215823992T>C g.215650650T>C USH2A c.14285A>G, p.N4762S - USH2A_000580 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease AXLM_9 PubMed: Zhu 2021 family 28, patient AXLM_9 F - China - - - - - 1 LOVD
?/. - c.14285A>G r.(?) p.(Asn4762Ser) - Unknown ACMG VUS g.215823992T>C g.215650650T>C - - USH2A_000580 ACMG GN005 criteria: PM2_P PM3_M PubMed: Meng, X. et al., 2021; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Sun, Y. et al., 2020 - rs1254637647 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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