Variant #0000953340 (NC_000001.10:g.215932092dup, NM_206933.2:c.11234dup (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.215932092dup
DNA change (hg38) g.215758750dup
Published as 11234dupA
ISCN -
DB-ID USH2A_000186 See all 4 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P PM3_M
Reference PubMed: Aller, E. et al., 2006
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-12-12 17:01:57 +01:00 (CET)
Date last edited 2023-12-13 17:38:50 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
USH2A NM_206933.2 +/. - c.11234dup r.(?) p.(Tyr3745Ter) -


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