Variant #0000953490 (NC_000001.10:g.215847775C>T, NM_206933.2:c.13478G>A (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.215847775C>T
DNA change (hg38) g.215674433C>T
Published as -
ISCN -
DB-ID USH2A_001142 See all 5 reported entries
Variant remarks ACMG GN005 criteria: BS2_S BP4_P
Reference PubMed: Huang, L. et al., 2018
ClinVar ID -
dbSNP ID rs138879998
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00044 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 17:03:48 +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.13478G>A r.(?) p.(Arg4493His) -


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.