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.

9 entries on 1 page. Showing entries 1 - 9.
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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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Tissue     

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Disease     

ID_report     

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Owner     
-?/. - c.3945T>C r.(?) p.(Asn1315=) - Unknown - likely benign g.216371793A>G g.216198451A>G USH2A(NM_206933.2):c.3945T>C (p.N1315=) - USH2A_000633 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.3945T>C r.(?) p.(Asn1315=) - Unknown - benign g.216371793A>G g.216198451A>G USH2A(NM_206933.2):c.3945T>C (p.N1315=) - USH2A_000633 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 18 c.3945T>C r.(?) p.(=) Fibronectin type-III 3 (1242-1357) Paternal (inferred) - benign g.216371793A>G g.216198451A>G - - USH2A_000633 Homozygous; Neutral PubMed: Le Quesne Stabej 2012 - rs41303257 Germline - 10/858 controls -NsiI;-HpyCH4V; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 18 c.3945T>C r.(?) p.(=) Fibronectin type-III 3 (1242-1357) Maternal (inferred) - benign g.216371793A>G g.216198451A>G - - USH2A_000633 Homozygous; Neutral PubMed: Le Quesne Stabej 2012 - rs41303257 Germline - 10/858 controls -NsiI;-HpyCH4V; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 18 c.3945T>C r.(?) p.(=) Fibronectin type-III 3 (1242-1357) Unknown - benign g.216371793A>G g.216198451A>G - - USH2A_000633 Heterozygous; Neutral PubMed: Le Quesne Stabej 2012 - rs41303257 Germline - 10/844 controls -NsiI;-HpyCH4V; - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 18 c.3945T>C r.(?) p.(=) Fibronectin type-III 3 (1242-1357) Unknown - benign g.216371793A>G g.216198451A>G - - USH2A_000633 Heterozygous; Neutral PubMed: Saihan 2011 - rs41303257 Germline - 10/844 controls -NsiI;-HpyCH4V; - - DNA SEQ - - retinal disease - PubMed: Saihan 2011 Proband F - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 18 c.3945T>C r.(?) p.(=) Fibronectin type-III 3 (1242-1357) Unknown - benign g.216371793A>G g.216198451A>G - - USH2A_000633 Heterozygous; UV2 PubMed: Jaijo 2010 - rs41303257 Germline - - -NsiI;-HpyCH4V; - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 18 c.3945T>C r.(?) p.(=) Fibronectin type-III 3 (1242-1357) Unknown - benign g.216371793A>G g.216198451A>G - - USH2A_000633 Heterozygous; Neutral PubMed: Baux 2014 - rs41303257 Germline - 10/844 controls -NsiI;-HpyCH4V; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/. - c.3945T>C r.(=) p.(=) - Parent #1 - benign g.216371793A>G g.216198451A>G - - USH2A_000633 90 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs41303257 Germline - 90/2795 individuals - - - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - 90 Mohammed Faruq
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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