Variant #0009715552 (NC_000016.9:g.16101669G>A, NC_000016.9(NM_004996.3):c.49-4G>A (ABCC1))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.16101669G>A
DB-ID -
dbSNP ID rs776425817
gnomAD frequency 2/240496
gnomAD homozygote count 0/120246
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     
ABCC1 NM_004996.3 ./. c.49-4G>A r.spl? p.?