Variant #0000953412 (NC_000001.10:g.215848910G>A, NM_206933.2:c.12343C>T (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.215848910G>A
DNA change (hg38) g.215675568G>A
Published as -
ISCN -
DB-ID USH2A_000050 See all 21 reported entries
Variant remarks ACMG GN005 criteria: BP2_P
Reference PubMed: Bonnet, C. et al., 2016; PubMed: Ganapathi, M. et al., 2022; PubMed: Jauregui, R. et al., 2020
ClinVar ID -
dbSNP ID rs111033275
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00032 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 17:03:01 +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.12343C>T r.(?) p.(Arg4115Cys) -


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