Variant #0000952895 (NC_000001.10:g.216363626_216363627del, NM_206933.2:c.4338_4339del (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.216363626_216363627del
DNA change (hg38) g.216190284_216190285del
Published as 4338_4339delCT
ISCN -
DB-ID USH2A_000007 See all 39 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P PM3_P
Reference PubMed: Wafa, T. T. et al., 2021
ClinVar ID -
dbSNP ID rs111033367
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner David Baux
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by David Baux
Date created 2023-12-12 16:53:36 +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.4338_4339del r.(?) p.(Cys1447GlnfsTer29) -


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