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.

17 entries on 1 page. Showing entries 1 - 17.
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+?/. - c.1211del r.(?) p.(Asn405Ilefs*3) - Both (homozygous) - likely pathogenic g.216497627del g.216324285del USH2A p.N405fs - USH2A_000199 no nucleotide annotation, extrapolated from protein and databases; heterozygous PubMed: Jacobson 2014 - - Unknown ? - - - - DNA ? - - retinal disease P34 PubMed: Jacobson 2014 - M - United States - - - - - 1 LOVD
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Heterozygous; Pathogenic PubMed: Jaijo 2010 - - Germline - - none - - DNA SEQ, SSCA - - USH - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Heterozygous PubMed: Bernal 2005 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Bernal 2005 Proband M - Spain - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Parent #2 - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Heterozygous PubMed: Shwartz 2005 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Shwartz 2005 Proband M - - - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Unknown - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Heterozygous PubMed: Sandberg 2008 - - Germline - - none - - DNA SEQ - - ? - PubMed: Sandberg 2008 Proband - USH2 or ARRP - - United States - - - - - 1 Anne-Françoise Roux
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Paternal (inferred) - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Homozygous; Pathogenic PubMed: Garcia-Garcia 2011 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Maternal (inferred) - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Homozygous; Pathogenic PubMed: Garcia-Garcia 2011 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Heterozygous; Pathogenic PubMed: Jaijo 2010 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Unknown - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Heterozygous; Pathogenic PubMed: Garcia-Garcia 2011 - - Germline - - none - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+/+ 7 c.1214del r.(?) p.(Asn405Ilefs*3) Laminin N-terminal (271-517) Unknown - pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 Heterozygous PubMed: Aparisi 2014 - - Germline - - none - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Aparisi 2014 Proband - - Spain - - - - - 1 Anne-Françoise Roux
+?/. - c.1214del r.(?) p.(Asn405IlefsTer3) - Parent #2 - likely pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 - PubMed: Perez-Carro 2016 - - Germline yes - - - - DNA SEQ-NG - gene panel retinal disease RP-1412 PubMed: Perez-Carro 2016 - - - Spain - - - - - 1 LOVD
+/. 7 c.1214del r.(?) p.(Asn405Ilefs*3) - Unknown - pathogenic g.216497624del - 2299delG (Glu767fs) - USH2A_000199 - PubMed: Jacobson 2008; PubMed: Schwartz 2005 - - Unknown - - - - - DNA SSCA - - retinal disease - PubMed: Jacobson 2008; PubMed: Schwartz 2005 Schwartz:F4-P1 M - - - - - - - 1 LOVD
+?/. - c.1214del r.(?) p.(Asn405Ilefs*3) - Maternal (confirmed) - likely pathogenic g.216497627del g.216324285del - - USH2A_000199 - PubMed: Perez-Carro 2018 - - Germline yes - - - - DNA SEQ-NG blood - retinal disease RP-1412 PubMed: Perez-Carro 2018 family RP-1412 F ? Spain - - - - - 1 LOVD
+?/. 7 c.1214del r.(?) p.(Asn405Ilefs*3) - Unknown - likely pathogenic g.216497627del g.216324285del USH2A Ex.7 c.1214del p.(Asn405Ilefs*3), Ex.13 c.2276G>T p.(Cys759Phe) - USH2A_000199 compound heterozygous PubMed: Martin Merida 2019 - - Germline yes - - - - DNA SEQ-NG-I - - retinal disease RP-1412 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. 7 c.1214del r.(?) p.(Asn405Ilefs*3) - Unknown - likely pathogenic g.216497627del g.216324285del USH2A Ex.7 c.1214del p.(Asn405Ilefs*3), Ex.35 c.6730G>T p.(Val2244Leu) - USH2A_000199 compound heterozygous PubMed: Martin Merida 2019 - - Germline/De novo (untested) ? - - - - DNA SEQ-NG-I - - retinal disease RP-2421 PubMed: Martin Merida 2019 - ? - Spain - - - - - 1 LOVD
+?/. 7 c.1214del r.(?) p.(Asn405Ilefs*3) - Unknown - likely pathogenic g.216497624del - c.1214delA,p.N405IfsX3 - USH2A_000199 - PubMed: Wafa-2021 - - Germline - - - - - DNA SEQ-NG, SEQ - - retinal disease - PubMed: Wafa 2021 - - - United States - - - - - 1 LOVD
+/. - c.1214del r.(?) p.(Asn405IlefsTer3) - Unknown ACMG pathogenic g.216497627del g.216324285del 1214delA - USH2A_000199 ACMG GN005 criteria: PVS1_VS PM2_P PM3_S PubMed: Perez-Carro, R. et al., 2018; PubMed: Garcia-Garcia, G. et al., 2011; PubMed: Garcia Bohorquez, B. et al., 2021; PubMed: Aparisi, M. J. et al., 2014 - rs750228923 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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