Variant #0001985306 (NC_000023.10:g.123205213C>T, NC_000023.10(NM_006603.4):c.2533+40C>T (STAG2))

Chromosome X
DNA change (genomic) (Relative to hg19 / GRCh37) g.123205213C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID STAG2_000091
Frequency 1/10563
Freq. EA 0/6728
Freq. AA 1/3835
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 16:50:35 +02:00 (CEST)
Date last edited 2024-12-10 09:46:12 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
STAG2 NM_006603.4 ?/? c.2533+40C>T r.(=) p.(=)