Variant #0004955588 (NC_000007.13:g.48232559C>T, NM_152701.3:c.73C>T (ABCA13))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48232559C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/114426
gnomAD homozygote count 0/57202
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     
ABCA13 NM_152701.3 ./. c.73C>T r.(?) p.(Leu25Phe)