Variant #0000520389 (NC_000003.11:g.52537010C>T, NC_000003.11(NM_015136.2):c.584-5C>T (STAB1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.52537010C>T
DNA change (hg38) g.52502994C>T
Published as STAB1(NM_015136.2):c.584-5C>T (p.?)
ISCN -
DB-ID STAB1_000004
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00745 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-08-04 19:28:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STAB1 NM_015136.2 -?/. - c.584-5C>T r.spl? p.?
NT5DC2 NM_022908.2 -?/. - c.*21476G>A r.(=) p.(=)


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