Variant #0009871800 (NC_000016.9:g.48212592C>G, NM_032583.3:c.3264delGinsC (ABCC11))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48212592C>G
DB-ID -
dbSNP ID rs138522850
gnomAD frequency 1/246080
gnomAD homozygote count 0/121252
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.3264delGinsC r.(?) p.(Ala1088=)
ABCC11 NM_033151.3 ./. c.3264delGinsC r.(?) p.(Ala1088=)
ABCC11 NM_145186.2 ./. c.3264delGinsC r.(?) p.(Ala1088=)