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.

5 entries on 1 page. Showing entries 1 - 5.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

P-domain     

Allele     

Classification method     

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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Segregation     

Frequency     

Re-site     

VIP     

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Template     

Technique     

Tissue     

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Disease     

ID_report     

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VIP     

Data_av     

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Panel size     

Owner     
-/. - c.1731C>T r.(?) p.(Cys577=) - Unknown - benign g.216465626G>A g.216292284G>A USH2A(NM_206933.4):c.1731C>T (p.C577=) - USH2A_000568 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 10 c.1731C>T r.(?) p.(=) Laminin EGF-like 2 (575-640) Unknown - benign g.216465626G>A g.216292284G>A - - USH2A_000568 Heterozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs41313732 Germline - 2/846 controls -HpyCH4V - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 10 c.1731C>T r.(?) p.(=) Laminin EGF-like 2 (575-640) Paternal (inferred) - benign g.216465626G>A g.216292284G>A - - USH2A_000568 Homozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs41313732 Germline - 2/844 controls -HpyCH4V - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-/- 10 c.1731C>T r.(?) p.(=) Laminin EGF-like 2 (575-640) Maternal (inferred) - benign g.216465626G>A g.216292284G>A - - USH2A_000568 Homozygous; UV1 PubMed: Le Quesne Stabej 2012 - rs41313732 Germline - 2/844 controls -HpyCH4V - - DNA SEQ - - USH2 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
-?/. - c.1731C>T r.(?) p.(Cys577=) - Both (homozygous) - likely benign g.216465626G>A g.216292284G>A - - USH2A_000568 - PubMed: Maranha 2015, Journal: Maranhao 2015 - rs41313732 Germline - - - - - DNA SEQ WBC - retinal disease PKRD138;61138 PubMed: Maranha 2015, Journal: Maranhao 2015, PubMed: Li 2017 - F yes Pakistan Pakistani - - - - 1 James Hejtmancik
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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