Variant #0000591041 (NC_000001.10:g.94980663C>T, NM_002858.3:c.1846-39delCinsT (ABCD3))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.94980663C>T
DB-ID -
dbSNP ID rs551093519
gnomAD frequency 0/244130
gnomAD homozygote count 0/122061
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     
ABCD3 NM_002858.3 ./. c.1846-39delCinsT r.(=) p.(=)