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.

11 entries on 1 page. Showing entries 1 - 11.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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DNA change (genomic) (hg19)     

DNA change (hg38)     

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Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
+/. - c.14384T>G r.(?) p.(Leu4795Arg) - Unknown - pathogenic g.215822068A>C g.215648726A>C - - USH2A_000502 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.14384T>G r.(?) p.(Leu4795Arg) - Unknown - pathogenic g.215822068A>C g.215648726A>C - - USH2A_000502 - PubMed: Haer-Wigman 2017 - - Germline - - - - - DNA SEQ-NG - gene panel ? 864 PubMed: Haer-Wigman 2017 family - no Netherlands - - - - - 1 LOVD
+/. 66 c.14384T>G r.(?) p.(Leu4795Arg) - Parent #1 - pathogenic (recessive) g.215822068A>C g.215648726A>C - - USH2A_000502 - PubMed: Dad 2016 - - Germline - - - - - DNA SEQ-NG - gene panel USH retinal disease USH2-20 PubMed: Dad 2016 - F no Denmark - - - - - 1 LOVD
+/. 66 c.14384T>G r.(?) p.(Leu4795Arg) - Parent #2 - pathogenic (recessive) g.215822068A>C g.215648726A>C - - USH2A_000502 possible duplicate PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - - Germline - - - - - DNA SEQ - - retinal disease USH2-61 (D27) PubMed: Dreyer 2000, PubMed: Dreyer 2008, PubMed: Dad 2016 - F no Denmark - - - - - 1 Anne-Françoise Roux
+?/. 66 c.14384T>G r.(14384u>g) p.(Leu4795Arg) - Parent #1 ACMG likely pathogenic g.215822068A>C g.215648726A>C - - USH2A_000502 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0114 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+?/. 66 c.14384T>G r.(14384u>g) p.(Leu4795Arg) - Parent #2 ACMG likely pathogenic g.215822068A>C g.215648726A>C - - USH2A_000502 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W02-142 Journal: Reurink 2021 - - - Netherlands - - - - - 1 Janine Reurink
+?/. 66 c.14384T>G r.(14384u>g) p.(Leu4795Arg) - Parent #2 ACMG likely pathogenic g.215822068A>C g.215648726A>C - - USH2A_000502 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0115 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+?/. - c.14384T>G r.(?) p.(Leu4795Arg) - Parent #1 ACMG likely pathogenic g.215822068A>C g.215648726A>C USH2A c.14384T>G, p.(Leu4795Arg) - USH2A_000502 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0114 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+?/. - c.14384T>G r.(?) p.(Leu4795Arg) - Parent #2 ACMG likely pathogenic g.215822068A>C g.215648726A>C USH2A c.14384T>G, p.(Leu4795Arg) - USH2A_000502 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W02-142 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+?/. - c.14384T>G r.(?) p.(Leu4795Arg) - Parent #2 ACMG likely pathogenic g.215822068A>C g.215648726A>C USH2A c.14384T>G, p.(Leu4795Arg) - USH2A_000502 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0115 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
?/. - c.14384T>G r.(?) p.(Leu4795Arg) - Unknown ACMG VUS g.215822068A>C g.215648726A>C - - USH2A_000502 ACMG GN005 criteria: PM2_P PM3_M PP3_P PubMed: Reurink, J. et al., 2021 - rs199851839 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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