Variant #0008891886 (NC_000014.8:g.74753487C>T, NM_005050.3:c.1669delGinsA (ABCD4))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74753487C>T
DB-ID -
dbSNP ID rs747712420
gnomAD frequency 3/246038
gnomAD homozygote count 0/123008
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCD4 NM_005050.3 ./. c.1669delGinsA r.(?) p.(Glu557Lys)