Variant #0000104006 (NC_000001.10:g.114429903C>T, NC_000001.10(NR_037864.1):n.247-10587C>T (AP4B1-AS1))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.114429903C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BCL2L15_000030
Frequency 1/13006
Freq. EA 1/8600
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 19:19:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BCL2L15 NM_001010922.2 ?/? c.95G>A r.(?) p.(Arg32Gln)
AP4B1-AS1 NR_037864.1 ?/? n.247-10587C>T r.(?) p.(Arg32Gln)