Variant #0006136752 (NC_000009.11:g.107665916G>A, NM_005502.3:c.45C>T (ABCA1))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.107665916G>A
DB-ID -
dbSNP ID rs137892737
gnomAD frequency 5/207724
gnomAD homozygote count 0/103857
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     
ABCA1 NM_005502.3 ./. c.45C>T r.(?) p.(Leu15=)