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.

19 entries on 1 page. Showing entries 1 - 19.
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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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DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Template     

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Disease     

ID_report     

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Owner     
+/+ 29 c.5836C>T r.(?) p.(Arg1946*) Fibronectin type-III 5 (1871-1949) Unknown - pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - -TaqI;-MlyI;-PleI;-HinfI; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 29 c.5836C>T r.(?) p.(Arg1946*) Fibronectin type-III 5 (1871-1949) Unknown - pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 Heterozygous PubMed: Baux 2014 - - Germline - - -TaqI;-MlyI;-PleI;-HinfI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 29 c.5836C>T r.(?) p.(Arg1946*) Fibronectin type-III 5 (1871-1949) Unknown - pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 Heterozygous PubMed: McGee 2010 - - Germline - - -TaqI;-MlyI;-PleI;-HinfI; - - DNA SEQ - - USH2 - PubMed: McGee 2010 No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-/- 29 c.5836C>T r.(?) p.(Arg1946*) Fibronectin type-III 5 (1871-1949) Unknown - pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 Heterozygous PubMed: Baux 2014 - - Germline - - -TaqI;-MlyI;-PleI;-HinfI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/. 29 c.5836C>T r.(?) p.(Arg1946*) Fibronectin type-III 5 (1871-1949) Parent #1 - pathogenic (recessive) g.216246252G>A - - - USH2A_000341 - PubMed: Ivanova 2018 - - Germline - - -TaqI;-MlyI;-PleI;-HinfI; - - DNA SEQ-NG-S - - USH2 Pat9 PubMed: Ivanova 2018 - F - Russian Federation Slavonian - - - - 1 Vladimir Strelnikov
+/. - c.5836C>T r.(?) p.(Arg1946Ter) - Unknown - pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.5836C>T r.(?) p.(Arg1946*) - Parent #2 - pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 - PubMed: Zenteno 2020 - - Germline - 1/143 cases - - - DNA SEQ, SEQ-NG - 199 gene panel retinal disease 2822 PubMed: Zenteno 2020 family - - Mexico - - - - - 1 Johan den Dunnen
+?/. - c.5836C>T r.(?) p.(Arg1946*) - Parent #1 - likely pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 575 PubMed: Stone 2017 1 affected F - (United States) - - - - - 1 LOVD
+?/. - c.5836C>T r.(?) p.(Arg1946*) - Parent #1 - likely pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 - PubMed: Stone 2017 - - Germline - - - - - DNA SEQ-NG - - retinal disease 576 PubMed: Stone 2017 family, 3 affected F - (United States) - - - - - 3 LOVD
+?/. - c.5836C>T r.(?) p.(Arg1946Ter) - Unknown - likely pathogenic (recessive) g.216246252G>A g.216072910G>A - - USH2A_000341 - PubMed: Xu 2014 - - Germline - 1/314 case chromosomes - - - DNA SEQ-NG - gene panel retinal disease RP273 PubMed: Xu 2014 - - - China - - - - - 1 LOVD
+?/. - c.5836C>T r.(?) p.(Arg1946*) - Unknown - likely pathogenic g.216246252G>A g.216072910G>A c.7843delC; p.Arg1946Ter:c.5836C/T(alleles in trans) - USH2A_000341 - PubMed: Hariri 2018 - - Germline ? - - - - DNA SEQ - retrospective analysis retinal disease - PubMed: Hariri 2018 - ? - - - - - - - 1 LOVD
+/. - c.5836C>T r.(?) p.(Arg1946*) - Unknown ACMG pathogenic g.216246252G>A g.216072910G>A USH2A c.5836C>T(;)10859T>C, V1: c.5836C>T, (p.Arg1946Ter) - USH2A_000341 alleles in cis or trans; heterozygous PubMed: Chen 2021 - - Unknown ? - - - - DNA SEQ-NG blood 212 inherited retinal disease-related genes retinal disease F297 PubMed: Chen 2021 - ? - Taiwan - - - - - 1 LOVD
+?/. - c.5836C>T r.(?) p.(Arg1946*) - Parent #1 - likely pathogenic g.216246252G>A g.216072910G>A USH2A c.5836C>T - USH2A_000341 protein variant annotation not written; heterozygous PubMed: Toms 2020 - - Unknown ? - - - - ? ? - retrospective cohort retinal disease 1 PubMed: Toms 2020 - ? - United Kingdom (Great Britain) - - - - - 1 LOVD
+/. - c.5836C>T r.(?) p.(Arg1946*) - Parent #1 - pathogenic g.216246252G>A g.216072910G>A USH2A c.5836C>T, p.Arg1946* - USH2A_000341 heterozygous PubMed: Gao 2021 - - Unknown ? - - - - DNA SEQ-NG - targeted (panel) sequencing USH R018090252 PubMed: Gao 2021 - M - China - - - - - 1 LOVD
+/. 29 c.5836C>T r.(?) p.(Arg1946*) - Parent #1 ACMG pathogenic g.216246252G>A g.216072910G>A USH2A c.C5836T, p.R1946* - USH2A_000341 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1644 PubMed: Zhu 2021 family 149, patient SRF_1644 M - China - - - - - 1 LOVD
+/. 29 c.5836C>T r.(?) p.(Arg1946*) - Parent #1 ACMG pathogenic g.216246252G>A g.216072910G>A USH2A c.5836C>T, p.R1946* - USH2A_000341 - PubMed: Zhu 2021 - - Germline yes - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_2009 PubMed: Zhu 2021 family 99, patient SRF_2009 M - China - - - - - 1 LOVD
+/. 29 c.5836C>T r.(?) p.(Arg1946*) - Parent #2 ACMG pathogenic g.216246252G>A g.216072910G>A USH2A c.5836C>T, p.R1946* - USH2A_000341 - PubMed: Zhu 2021 - - Unknown ? - - - - DNA SEQ-NG-I blood targeted sequencing retinal disease SRF_1645 PubMed: Zhu 2021 family 150, patient SRF_1645 F - China - - - - - 1 LOVD
+/. - c.5836C>T r.(?) p.(Arg1946Ter) - Unknown - pathogenic g.216246252G>A g.216072910G>A USH2A c.5836C>T(;)10859T>C; p.(Arg1946Ter) - USH2A_000341 heterozygous PubMed: Chen 2021 - - Germline/De novo (untested) ? Taiwan Biobank: 0; GnomAD_exome_East: 0.000109; GnomAD_All: 0.0000119 - - - DNA SEQ-NG - targeted 212 IRD-related genes retinal disease F297 PubMed: Chen 2021 - - - Taiwan - - - - - 1 LOVD
+/. - c.5836C>T r.(?) p.(Arg1946Ter) - Unknown ACMG pathogenic g.216246252G>A g.216072910G>A - - USH2A_000341 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Gao, F. J. et al., 2021; PubMed: Le Quesne Stabej, P. et al., 2012 - rs751130485 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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