Variant #0000018718 (NC_000019.9:g.11105608T>C, NM_003072.3:c.1524T>C (SMARCA4))

Chromosome 19
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.11105608T>C
DNA change (hg38) g.10994932T>C
Published as -
ISCN -
DB-ID SMARCA4_000038 See all 18 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.32796 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 2025-03-11 14:43:05 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCA4 NM_003072.3 ?/? - c.1524T>C r.(=) p.(=)


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