Variant #0006378487 (NC_000009.11:g.139927522C>T, NM_001606.4:c.-4930G>A (ABCA2))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.139927522C>T
DB-ID -
dbSNP ID rs757746166
gnomAD frequency 1/244452
gnomAD homozygote count 0/122225
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA2 NM_001606.4 ./. c.-4930G>A r.(=) p.(=)
FUT7 NM_004479.3 ./. c.-1079G>A r.(=) p.(=)
C9orf139 NM_207511.1 ./. c.7C>T r.(?) p.(Leu3=)
ABCA2 NM_212533.2 ./. c.-4198G>A r.(=) p.(=)