Variant #0002944619 (NC_000003.11:g.183682953C>T, NM_005688.2:c.2031+20delGinsA (ABCC5))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.183682953C>T
DB-ID -
dbSNP ID rs762054227
gnomAD frequency 8/245266
gnomAD homozygote count 0/122614
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     
ABCC5 NM_005688.2 ./. c.2031+20delGinsA r.(=) p.(=)