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.

20 entries on 1 page. Showing entries 1 - 20.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

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Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
+/+ 47i c.9371+1G>C r.spl p.? - Unknown - pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - 1/866 controls +AluI;+CviKI_1;-CviQI;-RsaI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 47i c.9371+1G>C r.spl p.? - Unknown - pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 Heterozygous PubMed: Lenassi 2015 - - Germline - - +AluI;+CviKI_1;-CviQI;-RsaI; - - DNA SEQ - - RPar - PubMed: Lenassi 2015 Proband - - United Kingdom (Great Britain) - - - - - 1 Eva Lenassi
+/+ 47i c.9371+1G>C r.spl p.? - Paternal (confirmed) - pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 Heterozygous; mutation PubMed: Shu 2015 - - Germline - - +AluI;+CviKI_1;-CviQI;-RsaI; - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Shu 2015 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 47i c.9371+1G>C r.spl p.? - Parent #2 - pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/. - c.9371+1G>C r.spl p.? - Parent #2 - pathogenic (recessive) g.216011332C>G g.215837990C>G - - USH2A_000592 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP309 PubMed: Xu 2014 patient F - China - - - - - 1 LOVD
+/. - c.9371+1G>C r.spl p.? - Unknown - pathogenic (recessive) g.216011332C>G g.215837990C>G - - USH2A_000592 - PubMed: Xu 2014 - - Germline - - - - - DNA SEQ-NG - gene panel retinal disease RP331 PubMed: Xu 2014 patient M - China - - - - - 1 LOVD
+/. - c.9371+1G>C r.spl p.? - Parent #2 - pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 - PubMed: Zhao 2015 - - Germline - - - - - DNA SEQ-NG - 86-gene panel retinal disease Rp170 PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - 1 LOVD
+/. - c.9371+1G>C r.spl p.? - Unknown - pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 - PubMed: Zhao 2015 - - Germline - - - - - DNA SEQ-NG - 86-gene panel retinal disease Rp400B PubMed: Zhao 2015 simplex case - - Northern Ireland - - - - - 1 LOVD
+/. 47i c.9371+1G>C r.spl p.? - Parent #1 ACMG pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0924 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+/. 47i c.9371+1G>C r.spl p.? - Parent #2 ACMG pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 - Journal: Reurink 2021 - - Germline no - - - - DNA SEQ-NG - gene panel retinal disease W19-0921 Journal: Reurink 2021 - - - - - - - - - 1 Janine Reurink
+?/. - c.9371+1G>C r.spl p.(?) - Unknown - likely pathogenic g.216011332C>G g.215837990C>G USH2A;NM_206933.2;c.[11699A>G];[9371+1G>C];p.[(Tyr3900Cys)];[?] - USH2A_000592 compound heterozygous PubMed: Jiman 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 176 genes panel retinal disease 21 PubMed: Jiman 2020 - F - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. 47i c.9371+1G>C r.spl? p.? - Unknown - likely pathogenic g.216011332C>G - IVS47+1G>C - USH2A_000592 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 47i c.9371+1G>C r.spl? p.? - Unknown - likely pathogenic g.216011332C>G - IVS47+1G>C - USH2A_000592 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. - c.9371+1G>C r.spl p.(?) - Parent #2 - likely pathogenic g.216011332C>G g.215837990C>G USH2A c.9371+1G>C, p.(?) - USH2A_000592 heterozygous PubMed: Molina-Ramirez 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 14 patients: 105-gene panel, 13 samples: 176-gene panel using previously described method (O', Sullivan J et al. 2012) USH 14014093 PubMed: Molina-Ramirez 2020 - F - United Kingdom (Great Britain) - - - - - 1 LOVD
+?/. - c.9371+1G>C r.spl p.(?) - Parent #2 - likely pathogenic g.216011332C>G g.215837990C>G USH2A c.9371+1G>C, p.? - USH2A_000592 heterozygous PubMed: Molina-Ramirez 2020 - - Unknown ? - - - - DNA SEQ-NG-I - 14 patients: 105-gene panel, 13 samples: 176-gene panel using previously described method (O', Sullivan J et al. 2012) retinal disease 15011185 PubMed: Molina-Ramirez 2020 - M - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.9371+1G>C r.(?) p.(?) - Parent #1 ACMG pathogenic g.216011332C>G g.215837990C>G USH2A c.9371+1G>C, p.(?) - USH2A_000592 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0924 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. - c.9371+1G>C r.(?) p.(?) - Parent #2 ACMG pathogenic g.216011332C>G g.215837990C>G USH2A c.9371+1G>C, p.(?) - USH2A_000592 heterozygous PubMed: Reurink 2021 - - Unknown ? - - - - DNA SEQ-NG-I - molecular inversion probe-based sequencing retinal disease W19-0921 PubMed: Reurink 2021 genetically unexplained subjects from centers in the Netherlands, Ireland and Poland ? - Netherlands - - - - - 1 LOVD
+/. 47i c.9371+1G>C r.spl p.? - Parent #2 ACMG pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease arRP11 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+/. 47i c.9371+1G>C r.spl p.? - Parent #2 ACMG pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 - PubMed: Reurink 2023, Journal: Reurink 2023 - - Germline - - - - - DNA SEQ-NG - WGS retinal disease USH19 PubMed: Reurink 2023, Journal: Reurink 2023 - - - - - - - - - 1 Janine Reurink
+/. - c.9371+1G>C r.spl p.? - Unknown ACMG pathogenic g.216011332C>G g.215837990C>G - - USH2A_000592 ACMG GN005 criteria: PVS1_VS PM2_P PM3_P PubMed: Lenassi, E. et al., 2015; PubMed: Molina-Ramirez, L. P. et al., 2020; PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Shu, H. R. et al., 2015; PubMed: Wafa, T. T. et al., 2021 - rs41308425 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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