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.

8 entries on 1 page. Showing entries 1 - 8.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

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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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Re-site     

VIP     

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Template     

Technique     

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Disease     

ID_report     

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VIP     

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Owner     
+/+ 6 c.852_853del r.(?) p.(Glu284Aspfs*38) Laminin N-terminal (271-517) Unknown - pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 Heterozygous; Pathogenic PubMed: Le Quesne Stabej 2012 - - Germline - - +XcmI - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 6 c.852_853del r.(?) p.(Glu284Aspfs*38) Laminin N-terminal (271-517) Unknown - pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 Heterozygous PubMed: Seyedahmadi 2004 - - Germline - - +XcmI - - DNA SEQ - - USH2 - PubMed: Seyedahmadi 2004 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 6 c.852_853del r.(?) p.(Glu284Aspfs*38) Laminin N-terminal (271-517) Unknown - pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 Heterozygous PubMed: Seyedahmadi 2004 - - Germline - - +XcmI - - DNA SEQ - - USH2 - PubMed: Seyedahmadi 2004 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 6 c.852_853del r.(?) p.(Glu284Aspfs*38) Laminin N-terminal (271-517) Unknown - pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 Heterozygous PubMed: Seyedahmadi 2004 - - Germline - - +XcmI - - DNA SEQ - - RPar - PubMed: Seyedahmadi 2004 Proband - - United States - - - - - 1 Anne-Françoise Roux
+/+ 6 c.852_853del r.(?) p.(Glu284Aspfs*38) Laminin N-terminal (271-517) Maternal (confirmed) - pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 Heterozygous PubMed: Baux 2014 - - Germline - - +XcmI - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
+/+ 6 c.852_853del r.(?) p.(Glu284Aspfs*38) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband - - France - - - - - 1 Crystel Bonnet
+/+ 6 c.852_853del r.(?) p.(Glu284Aspfs*38) Laminin N-terminal (271-517) Parent #1 - pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 Heterozygous; mutation PubMed: Bonnet 2016 - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband F - France - - - - - 1 Crystel Bonnet
+/. - c.852_853del r.(?) p.(Glu284AspfsTer38) - Unknown ACMG pathogenic g.216498942_216498943del g.216325600_216325601del 852_853delGA - USH2A_000210 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012 - rs1188025733 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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