Variant #0002949351 (NC_000003.11:g.183899003_183899005del, NM_018358.2:c.-4993_-4991del (ABCF3))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.183899003_183899005del
DB-ID -
dbSNP ID rs753080941
gnomAD frequency 1/246232
gnomAD homozygote count 0/123115
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AP2M1 NM_001025205.1 ./. c.690_692del r.(?) p.(Thr231del)
AP2M1 NM_004068.3 ./. c.696_698del r.(?) p.(Thr233del)
ABCF3 NM_018358.2 ./. c.-4993_-4991del r.(=) p.(=)