Variant #0000878286 (NC_000005.9:g.139493808_139493809del, NM_005859.4:c.42_43del (PURA))

Chromosome 5
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.139493808_139493809del
DNA change (hg38) g.140114223_140114224del
Published as -
ISCN -
DB-ID PURA_000059
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Dai Weiqian
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Dai Weiqian
Date created 2022-09-14 11:08:15 +02:00 (CEST)
Date last edited 2022-09-15 14:48:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PURA NM_005859.4 +?/. - c.42_43del r.(?) p.(Leu15Glyfs*185)



Screenings

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