Variant #0000018877 (NC_000009.11:g.2086804G>A, NC_000009.11(NM_003070.3):c.2527-25G>A (SMARCA2))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2086804G>A
DNA change (hg38) g.2086804G>A
Published as -
ISCN -
DB-ID SMARCA2_000043 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.04729 View details
Owner Gijs Santen
Database submission license Creative Commons Attribution-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-06-28 17:52:20 +02:00 (CEST)
Date last edited 2025-06-08 16:11:24 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCA2 NM_003070.3 ?/? - c.2527-25G>A r.(=) p.(=)


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