Variant #0010781219 (NC_000017.10:g.66920993G>C, NM_007168.2:c.1291delCinsG (ABCA8))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.66920993G>C
DB-ID -
dbSNP ID rs149873456
gnomAD frequency 1/245754
gnomAD homozygote count 0/122823
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     
ABCA8 NM_007168.2 ./. c.1291delCinsG r.(?) p.(Arg431Gly)