Variant #0000120972 (NC_000001.10:g.153603146T>C, NC_000001.10(NM_005979.2):c.-2727A>G (S100A13))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.153603146T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID S100A13_000031
Frequency 3/13006
Freq. EA 3/8600
Freq. AA 0/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 19:41:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
S100A13 NM_005979.2 ?/? c.-2727A>G r.(=) p.(=)
S100A1 NM_006271.1 ?/? c.141+8T>C r.(=) p.(=)