Variant #0001176101 (NC_000012.11:g.8988835C>T, NC_000012.11(NM_144670.4):c.644-16C>T (A2ML1))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.8988835C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID A2ML1_000067
Frequency 1/12252
Freq. EA 0/8310
Freq. AA 1/3942
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 16:39:18 +02:00 (CEST)
Date last edited 2018-08-23 10:11:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A2ML1 NM_144670.4 ?/? c.644-16C>T r.(=) p.(=)