Variant #0000897863 (NC_000001.10:g.215972249C>A, NM_206933.2:c.9958G>T (USH2A))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method ACMG
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.215972249C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID USH2A_000877 See all 41 reported entries
Variant remarks mini-gene splicing assay; changes ACMG to likely pathogenic
Reference PubMed: Reurink 2022, Journal: Reurink 2022
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Janine Reurink
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-11-04 17:14:15 +01:00 (CET)
Date last edited 2022-11-15 15:16:07 +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 +?/. 50 c.9958G>T r.[9958g>u,9898_9958del,9740_9958del] p.[Gly3320Cys,Ser3301Cysfs*9,Glu3248_Gly3320del] -


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