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.

14 entries on 1 page. Showing entries 1 - 14.
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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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ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

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Disease     

ID_report     

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Owner     
+/. 4i_9i c.(784+1_749-1)_(1644++1_1645-1)del r.? p.? - Parent #2 - pathogenic (recessive) g.? - del ex5_9 - USH2A_000000 {PMID:Garcia-Garcia 2014:25352746}, {PMID:Fuster-Garcia 2018:30459346} - - - Germline - - - - - DNA SEQ - - USH2 RP1638 PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+/. - c.? r.? p.? - Parent #2 ACMG pathogenic (recessive) g.? - c.11381+1delG - USH2A_000000 variant unknown, no splice site at c.11381+1 PubMed: Sun 2018 - - Germline - - - - - DNA SEQ - - HL 19758 PubMed: Sun 2018 family - no China - - - - - 1 LOVD
+?/. - c.? r.0? p.0? - Unknown - likely pathogenic g.216240159_222780953del - chr1:g.216240159_222780953del - USH2A_000000 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G001037 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.? r.0? p.0? - Unknown - likely pathogenic g.216259365_216318209del - chr1:g.216259365_216318209del - USH2A_000000 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G005191 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.? r.0? p.0? - Unknown - likely pathogenic g.215958623_215961591del - chr1:g.215958623_215961591del - USH2A_000000 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G005258 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - (United Kingdom (Great Britain)) - - - - - 1 LOVD
+?/. - c.? r.0? p.0? - Unknown - likely pathogenic g.216009683_216011948del - chr1:g.216009683_216011948del - USH2A_000000 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease G008167 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - 1 LOVD
+?/. - c.? r.0? p.0? - Unknown - likely pathogenic g.215836170_215851932del - chr1:g.215836170_215851932del - USH2A_000000 heterozygous PubMed: Turro 2020 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I blood whole genome sequencing retinal disease W000148 PubMed: Turro 2020 only individuals with mutations in retinal disease genes from this publication were inserted into LOVD ? - - - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Unknown - likely pathogenic g.? - p.W3955* - USH2A_000000 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Unknown - likely pathogenic g.? - p.Q2201* - USH2A_000000 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Unknown - likely pathogenic g.? - p.W2133* - USH2A_000000 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Unknown - likely pathogenic g.? - p.R4935* - USH2A_000000 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Unknown - likely pathogenic g.? - R1281* - USH2A_000000 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Both (homozygous) - likely pathogenic g.? - p.W3955* - USH2A_000000 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+?/. 2 c.? r.(?) p.? - Unknown - likely pathogenic g.? - p.G3142* - USH2A_000000 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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