Variant #0000953421 (NC_000001.10:g.215848844del, NM_206933.2:c.12409del (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.215848844del
DNA change (hg38) g.215675502del
Published as 12409delA
ISCN -
DB-ID USH2A_000964 See all 3 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P PM3_P
Reference PubMed: Jiang, L. et al., 2015
ClinVar ID -
dbSNP ID rs1657992342
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 17:03:01 +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.12409del r.(?) p.(Arg4137GlufsTer30) -


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