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.

22 entries on 1 page. Showing entries 1 - 22.
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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)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.2256T>C r.(?) p.(His752=) - Unknown - likely benign g.216420480A>G g.216247138A>G USH2A(NM_206933.2):c.2256T>C (p.H752=), USH2A(NM_206933.4):c.2256T>C (p.H752=) - USH2A_000055 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.2256T>C r.(?) p.(His752=) - Unknown - likely benign g.216420480A>G g.216247138A>G USH2A(NM_206933.2):c.2256T>C (p.H752=), USH2A(NM_206933.4):c.2256T>C (p.H752=) - USH2A_000055 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Parent #1 - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Baux 2007 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Baux 2007 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous - - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - RPar - - Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Aller 2004 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH - PubMed: Aller 2004 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Jaijo 2010 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Jaijo 2010 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Aller 2004 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH - PubMed: Aller 2004 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Aller 2004 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - RPar - PubMed: Aller 2004 Proband F - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Najera 2002 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Najera 2002 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Paternal (confirmed) - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Baux 2014 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Paternal (inferred) - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Homozygous PubMed: Baux 2014 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Maternal (inferred) - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Homozygous PubMed: Baux 2014 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Baux 2014 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous; Neutral PubMed: Garcia-Garcia 2011 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband F - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous; Neutral PubMed: Garcia-Garcia 2011 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH - PubMed: Garcia-Garcia 2011 Proband - - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Baux 2014 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Vaché 2012 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Vaché 2012 Proband F - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous; Neutral PubMed: Garcia-Garcia 2011 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Baux 2014 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
-/- 13 c.2256T>C r.(?) p.(=) Laminin EGF-like 5 (747-794) Unknown - benign g.216420480A>G g.216247138A>G - - USH2A_000055 Heterozygous PubMed: Baux 2014 - rs111033281 Germline - - +BceAI;-CviAII;-NcoI;-FatI; - - DNA SEQ, SEQ-NG-S - - USH1 - PubMed: Baux 2014 Proband - unclear USH phenotype M - France - - - - - 1 Anne-Françoise Roux
-?/. - c.2256T>C r.(?) p.(His752=) - Unknown - likely benign g.216420480A>G g.216247138A>G USH2A(NM_206933.2):c.2256T>C (p.H752=), USH2A(NM_206933.4):c.2256T>C (p.H752=) - USH2A_000055 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+?/. - c.2256T>C r.(?) p.(His752=) - Unknown - likely pathogenic g.216420480A>G g.216247138A>G - - USH2A_000055 - PubMed: Ellingford 2016 - - Germline - - - - - DNA SEQ - 105-gene panel retinal disease 12006031 PubMed: Ellingford 2016 familial segregation analysis requested - - - - - - - - 1 LOVD
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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