Variant #0011167888 (NC_000019.9:g.1036594C>T, NM_019112.3:c.-3739C>T (ABCA7))

Chromosome 19
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.1036594C>T
DB-ID -
dbSNP ID rs765294176
gnomAD frequency 1/244226
gnomAD homozygote count 0/122112
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+33C>T r.(=) p.(=)
ABCA7 NM_019112.3 ./. c.-3739C>T r.(=) p.(=)
CNN2 NM_201277.1 ./. c.537+33C>T r.(=) p.(=)