Variant #0000952691 (NC_000001.10:g.216498735G>A, NM_206933.2:c.1055C>T (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.216498735G>A
DNA change (hg38) g.216325393G>A
Published as -
ISCN -
DB-ID USH2A_000046 See all 24 reported entries
Variant remarks ACMG GN005 criteria: PM2_P PM3_VS PP3_P PP1_P
Reference PubMed: Falsini, B. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Colombo, L. et al., 2022; PubMed: Ganapathi, M. et al., 2022; PubMed: Mansard, L. et al., 2021; PubMed: Colombo, L. et al., 2021; PubMed: Eandi, C. M. et al., 2017
ClinVar ID -
dbSNP ID rs780308389
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-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 16:50:31 +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.1055C>T r.(?) p.(Thr352Ile) -


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