Variant #0000953626 (NC_000001.10:g.215799170T>C, NM_206933.2:c.15562A>G (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.215799170T>C
DNA change (hg38) g.215625828T>C
Published as -
ISCN -
DB-ID USH2A_000281 See all 15 reported entries
Variant remarks ACMG GN005 criteria: BA1 BS2_S BP4_P
Reference PubMed: Gao, F. J. et al., 2021; PubMed: Huang, X. F. et al., 2015
ClinVar ID -
dbSNP ID rs58257972
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01269 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 17:06:39 +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.15562A>G r.(?) p.(Ser5188Gly) -


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