Variant #0000952862 (NC_000001.10:g.216371897T>A, NM_206933.2:c.3841A>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.216371897T>A
DNA change (hg38) g.216198555T>A
Published as -
ISCN -
DB-ID USH2A_002577 See all 3 reported entries
Variant remarks ACMG GN005 criteria: PVS1_VS PM2_P
Reference PubMed: Le Quesne Stabej, P. et al., 2012; PubMed: Wafa, T. T. et al., 2021
ClinVar ID -
dbSNP ID rs2034908088
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 16:53:21 +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.3841A>T r.(?) p.(Arg1281Ter) -


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