Variant #0009872947 (NC_000016.9:g.48250026G>A, NM_032583.3:c.950delCinsT (ABCC11))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48250026G>A
DB-ID -
dbSNP ID rs11863236
gnomAD frequency 6/245300
gnomAD homozygote count 0/100873
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.950delCinsT r.(?) p.(Ala317Val)
ABCC11 NM_033151.3 ./. c.950delCinsT r.(?) p.(Ala317Val)
ABCC11 NM_145186.2 ./. c.950delCinsT r.(?) p.(Ala317Val)