Variant #0002949347 (NC_000003.11:g.183898972T>C, NM_018358.2:c.-5024T>C (ABCF3))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.183898972T>C
DB-ID -
dbSNP ID -
gnomAD frequency 11/246244
gnomAD homozygote count 0/123111
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     
AP2M1 NM_001025205.1 ./. c.659T>C r.(?) p.(Ile220Thr)
AP2M1 NM_004068.3 ./. c.665T>C r.(?) p.(Ile222Thr)
ABCF3 NM_018358.2 ./. c.-5024T>C r.(=) p.(=)