Variant #0000045644 (NC_000001.10:g.29522674C>T, NC_000001.10(NM_016011.2):c.891+36G>A (MECR))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.29522674C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MECR_000023
Frequency 3/13006
Freq. EA 0/8600
Freq. AA 3/4406
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 17:58:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MECR NM_016011.2 ?/? c.891+36G>A r.(=) p.(=)