Variant #0000953359 (NC_000001.10:g.215914895del, NC_000001.10(NM_206933.2):c.11549-5del (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.215914895del
DNA change (hg38) g.215741553del
Published as 11549-5delT
ISCN -
DB-ID USH2A_001340 See all 10 reported entries
Variant remarks ACMG GN005 criteria: BA1 BS2_S BP4_P
Reference PubMed: Gao, F. J. et al., 2021
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 17:02:17 +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.11549-5del r.(?) p.(=) -


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