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.
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     
+?/. - c.2710_2720dup r.(?) p.(Leu908Profs*63) - Unknown - likely pathogenic g.216420016_216420026dup g.216246674_216246684dup c.2710_2720dup, p.Leu908ProfsTer63 - USH2A_002335 heterozygous PubMed: Zampaglione 2020 - - Unknown ? - - - - DNA SEQ-NG-I, SEQ blood - retinal disease OGI2917_004502 PubMed: Zampaglione 2020 - ? - - - - - - - 1 LOVD
+/. 13 c.2710_2720dup r.(?) p.(Leu908Profs*63) - Unknown - pathogenic (recessive) g.216420016_216420026dup - c.2710_2720dup - USH2A_002335 - PubMed: Colombo-2020 - rs755218835 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. 13 c.2710_2720dup r.(?) p.(Leu908Profs*63) - Unknown - pathogenic g.216420016_216420026dup - c.2710_2720dup - USH2A_002335 - PubMed: Colombo-2020 - rs755218835 Germline yes - - - - DNA SEQ - - retinal disease - PubMed: Colombo-2020 - M no - - - - - - 1 LOVD
+/. - c.2710_2720dup r.(?) p.(Leu908ProfsTer63) - Unknown ACMG pathogenic g.216420016_216420026dup g.216246674_216246684dup - - USH2A_002335 ACMG GN005 criteria: PVS1_VS PM2_P PM3_M PubMed: Colombo, L. et al., 2022; PubMed: Colombo, L. et al., 2021 - rs755218835 SUMMARY record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.2710_2720dup r.(?) p.(Leu908ProfsTer63) - Maternal (confirmed) ACMG pathogenic (recessive) g.216420016_216420026dup g.216246674_216246684dup - - USH2A_002335 ACMG PM2, PVS1, PP5 PubMed: Weisschuh 2024 - - Germline - - - - - DNA SEQ-NG - WGS ? USHII-320 PubMed: Weisschuh 2024 patient, no family history F - Germany - - - - - 1 Johan den Dunnen
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.