Variant #0010679322 (NC_000017.10:g.48733316C>T, NM_003786.3:c.169C>T (ABCC3))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48733316C>T
DB-ID -
dbSNP ID rs200070901
gnomAD frequency 17/246208
gnomAD homozygote count 0/123086
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCC3 NM_001144070.1 ./. c.169C>T r.(?) p.(Arg57Trp)
ABCC3 NM_003786.3 ./. c.169C>T r.(?) p.(Arg57Trp)