Variant #0000953140 (NC_000001.10:g.216061824G>A, NM_206933.2:c.8167C>T (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.216061824G>A
DNA change (hg38) g.215888482G>A
Published as -
ISCN -
DB-ID USH2A_000181 See all 15 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P
Reference PubMed: Lee, S. Y. et al., 2020; PubMed: Garcia-Garcia, G. et al., 2014; PubMed: Jin, X. et al., 2022; PubMed: Mansard, L. et al., 2021
ClinVar ID -
dbSNP ID rs200712760
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-12-12 16:59:13 +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.8167C>T r.(?) p.(Arg2723Ter) -


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