Variant #0000590262 (NC_000001.10:g.94924137T>G, NC_000001.10(NM_002858.3):c.111-26T>G (ABCD3))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94924137T>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/245770
gnomAD homozygote count 0/122874
Average frequency (gnomAD v.2.1.1) 0 View details
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     
ABCD3 NM_001122674.1 ./. c.111-26T>G r.(=) p.(=)
ABCD3 NM_002858.3 ./. c.111-26T>G r.(=) p.(=)