Variant #0009872245 (NC_000016.9:g.48230282A>T, NM_032583.3:c.2315-50delTinsA (ABCC11))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48230282A>T
DB-ID -
dbSNP ID rs772595962
gnomAD frequency 1/216014
gnomAD homozygote count 0/107998
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.2315-50delTinsA r.(=) p.(=)
ABCC11 NM_033151.3 ./. c.2315-50delTinsA r.(=) p.(=)
ABCC11 NM_145186.2 ./. c.2315-50delTinsA r.(=) p.(=)