Variant #0002949420 (NC_000003.11:g.183899844_183899845del, NM_018358.2:c.-4152_-4151del (ABCF3))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.183899844_183899845del
DB-ID -
dbSNP ID rs764508843
gnomAD frequency 4/244206
gnomAD homozygote count 0/122091
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.957+9_957+10del r.(=) p.(=)
AP2M1 NM_004068.3 ./. c.963+9_963+10del r.(=) p.(=)
ABCF3 NM_018358.2 ./. c.-4152_-4151del r.(=) p.(=)