Variant #0002945413 (NC_000003.11:g.183732219G>A, NM_005688.2:c.-39C>T (ABCC5))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.183732219G>A
DB-ID -
dbSNP ID rs201676276
gnomAD frequency 54/213962
gnomAD homozygote count 0/106927
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     
ABCC5 NM_001023587.1 ./. c.-39C>T r.(=) p.(=)
ABCC5 NM_005688.2 ./. c.-39C>T r.(=) p.(=)