Variant #0009871266 (NC_000016.9:g.48177995C>G, NC_000016.9(NM_033226.2):c.120-19G>C (ABCC12))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48177995C>G
DB-ID -
dbSNP ID rs760745091
gnomAD frequency 2/239672
gnomAD homozygote count 0/119833
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     
ABCC12 NM_033226.2 ./. c.120-19G>C r.(=) p.(=)