Variant #0006378498 (NC_000009.11:g.139927541C>T, NM_001606.4:c.-4949G>A (ABCA2))

Chromosome 9
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.139927541C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/245198
gnomAD homozygote count 0/122598
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     
ABCA2 NM_001606.4 ./. c.-4949G>A r.(=) p.(=)
FUT7 NM_004479.3 ./. c.-1098G>A r.(=) p.(=)
C9orf139 NM_207511.1 ./. c.26C>T r.(?) p.(Pro9Leu)
ABCA2 NM_212533.2 ./. c.-4217G>A r.(=) p.(=)