Variant #0009873312 (NC_000016.9:g.48264524C>T, NC_000016.9(NM_032583.3):c.100-40G>A (ABCC11))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48264524C>T
DB-ID -
dbSNP ID rs760412601
gnomAD frequency 6/156310
gnomAD homozygote count 0/78149
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.100-40G>A r.(=) p.(=)
ABCC11 NM_033151.3 ./. c.100-40G>A r.(=) p.(=)
ABCC11 NM_145186.2 ./. c.100-40G>A r.(=) p.(=)