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.

4 entries on 1 page. Showing entries 1 - 4.
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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     
+/+ 30 c.5933_5940del r.(?) p.(Pro1978Glnfs*5) Fibronectin type-III 6 (1954-2051) Parent #2 - pathogenic g.216243553_216243560del g.216070211_216070218del - - USH2A_000388 Heterozygous PubMed: Sandberg 2008 - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Sandberg 2008 Proband - - United States - - - - - 1 Anne-Françoise Roux
+?/. - c.5933_5940del r.(?) p.(Pro1978Glnfs*5) - Both (homozygous) - likely pathogenic (recessive) g.216243553_216243560del g.216070211_216070218del - - USH2A_000388 - PubMed: Eandi 2017 - - Germline yes - - - - DNA SEQ-NG - 11-gene panel retinal disease Fam15PatTO19 PubMed: Eandi 2017 - M - Italy - - - - - 1 LOVD
+/. 30 c.5933_5940del r.(?) p.(Pro1978Glnfs*5) - Unknown - pathogenic (recessive) g.216243552_216243559del - c.5933_5940del - USH2A_000388 - PubMed: Colombo-2020 - - Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. - c.5933_5940del r.(?) p.(Pro1978GlnfsTer5) - Unknown ACMG pathogenic g.216243553_216243560del g.216070211_216070218del - - USH2A_000388 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2021; PubMed: Eandi, C. M. et al., 2017 - - SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
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All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


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