Variant #0002949405 (NC_000003.11:g.183899738T>C, NM_018358.2:c.-4258T>C (ABCF3))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.183899738T>C
DB-ID -
dbSNP ID rs757608518
gnomAD frequency 2/246236
gnomAD homozygote count 0/123116
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.860T>C r.(?) p.(Val287Ala)
AP2M1 NM_004068.3 ./. c.866T>C r.(?) p.(Val289Ala)
ABCF3 NM_018358.2 ./. c.-4258T>C r.(=) p.(=)