Variant #0009717628 (NC_000016.9:g.16230507C>T, NM_004996.3:c.4292+6delCinsT (ABCC1))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.16230507C>T
DB-ID -
dbSNP ID rs749961786
gnomAD frequency 263/244350
gnomAD homozygote count 2/121897
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.4292+6delCinsT r.(=) p.(=)