Variant #0000953220 (NC_000001.10:g.216011332C>G, NC_000001.10(NM_206933.2):c.9371+1G>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.216011332C>G
DNA change (hg38) g.215837990C>G
Published as -
ISCN -
DB-ID USH2A_000592 See all 20 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P PM3_P
Reference PubMed: Lenassi, E. et al., 2015; PubMed: Molina-Ramirez, L. P. et al., 2020; PubMed: Reurink, J. et al., 2021; PubMed: Bonnet, C. et al., 2016; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Shu, H. R. et al., 2015; PubMed: Wafa, T. T. et al., 2021
ClinVar ID -
dbSNP ID rs41308425
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 17:00:19 +01:00 (CET)
Date last edited 2023-12-13 17:38:50 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
USH2A NM_206933.2 +/. - c.9371+1G>C r.spl p.? -


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