Variant #0009719902 (NC_000016.9:g.16315502del, NC_000016.9(NM_001171.5):c.219+4delG (ABCC6))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.16315502del
DB-ID -
dbSNP ID rs758129215
gnomAD frequency 1/245570
gnomAD homozygote count 0/122784
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     
ABCC6 NM_001079528.3 ./. c.223delG r.(?) p.(Ala75LeufsTer23)
ABCC6 NM_001171.5 ./. c.219+4delG r.spl? p.?