Variant #0001720452 (NC_000019.9:g.11099987T>C, NC_000019.9(NM_003072.3):c.1119-6T>C (SMARCA4))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.11099987T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SMARCA4_000076
Frequency 4/13006
Freq. EA 3/8600
Freq. AA 1/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:45:39 +02:00 (CEST)
Date last edited 2013-05-05 23:12:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SMARCA4 NM_003072.3 ?/? c.1119-6T>C r.(=) p.(=)