Variant #0010785668 (NC_000017.10:g.67136753A>G, NM_080284.2:c.92T>C (ABCA6))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.67136753A>G
DB-ID -
dbSNP ID rs780907607
gnomAD frequency 3/231802
gnomAD homozygote count 0/115898
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     
ABCA6 NM_080284.2 ./. c.92T>C r.(?) p.(Leu31Ser)