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.

15 entries on 1 page. Showing entries 1 - 15.
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     
+?/. 54 c.10636G>A r.(?) p.(Gly3546Arg) - Both (homozygous) - likely pathogenic g.215955488C>T g.215782146C>T - - USH2A_000290 - PubMed: de Castro-Miró 2014 - - Germline - - - - - DNA SEQ-NG-I Whole blood - USH2A - PubMed: de Castro-Miró 2014 - F yes Spain - - - - - 1 Marta de Castro-Miró
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Paternal (inferred) ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Homozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy188I - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Maternal (inferred) ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Homozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy188I - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Unknown ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Heterozygous; UV3 PubMed: Vaché 2012, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy188I - - DNA SEQ - - USH2 - PubMed: Vaché 2012 Proband M - Spain - - - - - 1 Jose Maria Millan
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Paternal (inferred) ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Homozygous; Pathogenic PubMed: Garcia-Garcia 2011, USMA missense analysis, missense variant in MSV3d - - Germline - 0/200 controls +Hpy188I - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Maternal (inferred) ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Homozygous; Pathogenic PubMed: Garcia-Garcia 2011, USMA missense analysis, missense variant in MSV3d - - Germline - 0/200 controls +Hpy188I - - DNA SEQ - - USH2 - PubMed: Garcia-Garcia 2011 Proband M - Spain - - - - - 1 Jose Maria Millan
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Unknown ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Heterozygous; Pathogenic PubMed: Garcia-Garcia 2011, USMA missense analysis, missense variant in MSV3d - - Germline - 0/200 controls +Hpy188I - - DNA SEQ, SSCA - - USH2 - PubMed: Garcia-Garcia 2011 Proband F - Spain - - - - - 1 Jose Maria Millan
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Unknown ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Heterozygous PubMed: Baux 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy188I - - DNA SEQ - - USH2 - PubMed: Baux 2014 Proband M - France - - - - - 1 Anne-Françoise Roux
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Paternal (inferred) ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Homozygous; mutation PubMed: de Castro-Miro 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy188I - - DNA PE, SEQ - APEX USH2 - PubMed: de Castro-Miro 2014 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+?/? 54 c.10636G>A r.(?) p.(Gly3546Arg) Fibronectin type-III 20 (3499-3585) Maternal (inferred) ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 Homozygous; mutation PubMed: de Castro-Miro 2014, USMA missense analysis, missense variant in MSV3d - - Germline - - +Hpy188I - - DNA PE, SEQ - APEX USH2 - PubMed: de Castro-Miro 2014 Proband F - Spain - - - - - 1 Anne-Françoise Roux
+?/. - c.10636G>A r.(?) p.(Gly3546Arg) - Both (homozygous) - likely pathogenic g.215955488C>T g.215782146C>T - - USH2A_000290 - PubMed: Riera 2017 - - Germline yes - - - - DNA SEQ-NG - 212-gene panel retinal disease Fi15/37 PubMed: Riera 2017 patient - - Spain - - - - - 1 LOVD
+?/. 54 c.10636G>A r.(?) p.(Gly3546Arg) - Both (homozygous) - likely pathogenic g.215955488C>T - c.10636G>A - USH2A_000290 - PubMed: de Castro-Miró-2014 - - Germline - - - - - DNA PE - - retinal disease 40ORG PubMed: de Castro-Miró-2014 - - - - - - - - - 2 LOVD
+?/. - c.10636G>A r.(?) p.(Gly3546Arg) - Unknown ACMG likely pathogenic g.215955488C>T - - - USH2A_000290 - PubMed: Mansard et al, 2021 - rs1553261372 Germline - - - - - DNA SEQ-NG, SEQ - - USH2A - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. - c.10636G>A r.(?) p.(Gly3546Arg) - Unknown - likely pathogenic g.215955488C>T - - - USH2A_000290 - - - rs1553261372 Unknown - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.10636G>A r.(?) p.(Gly3546Arg) - Unknown ACMG VUS g.215955488C>T g.215782146C>T - - USH2A_000290 ACMG GN005 criteria: PM2_P PM3_M PubMed: Garcia-Garcia, G. et al., 2011; PubMed: Mansard, L. et al., 2021 - rs1553261372 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.