Variant #0009873352 (NC_000016.9:g.48265826T>C, NM_032583.3:c.7A>G (ABCC11))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48265826T>C
DB-ID -
dbSNP ID rs200128517
gnomAD frequency 165/246230
gnomAD homozygote count 0/122950
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     
ABCC11 NM_032583.3 ./. c.7A>G r.(?) p.(Arg3Gly)
ABCC11 NM_033151.3 ./. c.7A>G r.(?) p.(Arg3Gly)
ABCC11 NM_145186.2 ./. c.7A>G r.(?) p.(Arg3Gly)