Variant #0000953249 (NC_000001.10:g.215972408A>G, NM_206933.2:c.9799T>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.215972408A>G
DNA change (hg38) g.215799066A>G
Published as -
ISCN -
DB-ID USH2A_000176 See all 61 reported entries
Variant remarks ACMG GN005 criteria: PM2_P PM3_VS PP3_P
Reference PubMed: Gonzalez-Del Pozo, M. et al., 2018; PubMed: Garcia-Garcia, G. et al., 2011; PubMed: Perez-Carro, R. et al., 2018; PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Mansard, L. et al., 2021; PubMed: Aparisi, M. J. et al., 2014
ClinVar ID -
dbSNP ID rs111033263
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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 17:00:45 +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.9799T>C r.(?) p.(Cys3267Arg) -


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