Variant #0000953296 (NC_000001.10:g.215956104A>G, NM_206933.2:c.10561T>C (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.215956104A>G
DNA change (hg38) g.215782762A>G
Published as -
ISCN -
DB-ID USH2A_000429 See all 40 reported entries
Variant remarks ACMG GN005 criteria: PS4_S PM2_P PM3_VS
Reference PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Glockle, N. et al., 2014; PubMed: Weisschuh, N. et al., 2020; PubMed: Sloan-Heggen, C. M. et al., 2016; PubMed: Neuhaus, C. et al., 2017
ClinVar ID -
dbSNP ID rs111033264
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 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 17:01:23 +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.10561T>C r.(?) p.(Trp3521Arg) -


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