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.
Legend   How to query  

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     
-?/? 66 c.14519T>C r.(?) p.(Leu4840Pro) Fibronectin type-III 34 (4826-4927) Paternal (confirmed) ACMG likely benign g.215821933A>G g.215648591A>G - - USH2A_000248 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - France - - - - - 1 Anne-Françoise Roux
-?/? 66 c.14519T>C r.(?) p.(Leu4840Pro) Fibronectin type-III 34 (4826-4927) Unknown ACMG likely benign g.215821933A>G g.215648591A>G - - USH2A_000248 Heterozygous; unknown PubMed: McGee 2010, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ - - RPar - PubMed: McGee 2010 Proband - No genotype in the publication - - United States - - - - - 1 Anne-Françoise Roux
-?/? 66 c.14519T>C r.(?) p.(Leu4840Pro) Fibronectin type-III 34 (4826-4927) Parent #1 ACMG likely benign g.215821933A>G g.215648591A>G - - USH2A_000248 Homozygous PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
-?/? 66 c.14519T>C r.(?) p.(Leu4840Pro) Fibronectin type-III 34 (4826-4927) Parent #2 ACMG likely benign g.215821933A>G g.215648591A>G - - USH2A_000248 Homozygous PubMed: Bonnet 2016, USMA missense analysis, missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH2 - PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
?/. - c.14519T>C r.(?) p.(Leu4840Pro) - Unknown - VUS g.215821933A>G g.215648591A>G USH2A(NM_206933.2):c.14519T>C (p.L4840P), USH2A(NM_206933.4):c.14519T>C (p.L4840P) - USH2A_000248 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.14519T>C r.(?) p.(Leu4840Pro) - Unknown - VUS g.215821933A>G g.215648591A>G USH2A(NM_206933.2):c.14519T>C (p.L4840P), USH2A(NM_206933.4):c.14519T>C (p.L4840P) - USH2A_000248 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.14519T>C r.(?) p.(Leu4840Pro) - Unknown - VUS g.215821933A>G - USH2A(NM_206933.2):c.14519T>C (p.L4840P), USH2A(NM_206933.4):c.14519T>C (p.L4840P) - USH2A_000248 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.14519T>C r.(?) p.(Leu4840Pro) - Unknown ACMG VUS g.215821933A>G g.215648591A>G - - USH2A_000248 ACMG GN005 criteria: PubMed: Bonnet, C. et al., 2016 - rs143275144 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query  

All variants classified as SUMMARY RECORD have been extensively assessed by Dr. Luke Mansard.


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.