Variant #0000952779 (NC_000001.10:g.216424240C>T, NC_000001.10(NM_206933.2):c.2167+5G>A (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.216424240C>T
DNA change (hg38) g.216250898C>T
Published as -
ISCN -
DB-ID USH2A_000195 See all 22 reported entries
Variant remarks ACMG GN005 criteria: PS3_P PP3_P
Reference PubMed: Gao, F. J. et al., 2021; PubMed: Gonzalez-Del Pozo, M. et al., 2018; PubMed: Colombo, L. et al., 2022; PubMed: Mansard, L. et al., 2021; PubMed: Colombo, L. et al., 2021
ClinVar ID -
dbSNP ID rs771583281
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-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 16:51:47 +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.2167+5G>A r.(1972_2167del,2138_2167del) p.(Ile658GlyfsTer33,Gln714_Gly723del) -


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