Variant #0010679336 (NC_000017.10:g.48733352C>G, NM_003786.3:c.205C>G (ABCC3))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48733352C>G
DB-ID -
dbSNP ID rs148804178
gnomAD frequency 8/245980
gnomAD homozygote count 0/122980
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.205C>G r.(?) p.(Leu69Val)
ABCC3 NM_003786.3 ./. c.205C>G r.(?) p.(Leu69Val)