Variant #0010787646 (NC_000017.10:g.67243832C>G, NM_080282.3:c.-3755G>C (ABCA10))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.67243832C>G
DB-ID -
dbSNP ID rs376780755
gnomAD frequency 1/193972
gnomAD homozygote count 0/96985
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     
ABCA5 NM_018672.3 ./. c.4822-47G>C r.(=) p.(=)
ABCA10 NM_080282.3 ./. c.-3755G>C r.(=) p.(=)
ABCA5 NM_172232.2 ./. c.4822-47G>C r.(=) p.(=)