Variant #0011167884 (NC_000019.9:g.1036580del, NM_019112.3:c.-3753del (ABCA7))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.1036580del
DB-ID -
dbSNP ID rs750111327
gnomAD frequency 14/244918
gnomAD homozygote count 1/122446
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     
CNN2 NM_004368.2 ./. c.654+23delC r.(=) p.(=)
ABCA7 NM_019112.3 ./. c.-3753del r.(=) p.(=)
CNN2 NM_201277.1 ./. c.537+23delC r.(=) p.(=)