Variant #0008892851 (NC_000014.8:g.74769606C>T, NM_005050.3:c.10G>A (ABCD4))

Chromosome 14
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74769606C>T
DB-ID -
dbSNP ID rs139863822
gnomAD frequency 2/233944
gnomAD homozygote count 0/116602
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCD4 NM_005050.3 ./. c.10G>A r.(?) p.(Ala4Thr)