Variant #0010785659 (NC_000017.10:g.67136721G>T, NC_000017.10(NM_080284.2):c.96+28C>A (ABCA6))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.67136721G>T
DB-ID -
dbSNP ID rs572377812
gnomAD frequency 2/214902
gnomAD homozygote count 0/107436
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.96+28C>A r.(=) p.(=)