Variant #0002949429 (NC_000003.11:g.183899873C>T, NM_018358.2:c.-4123C>T (ABCF3))

Chromosome 3
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.183899873C>T
DB-ID -
dbSNP ID rs762029299
gnomAD frequency 1/242264
gnomAD homozygote count 0/121126
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.957+38C>T r.(=) p.(=)
AP2M1 NM_004068.3 ./. c.963+38C>T r.(=) p.(=)
ABCF3 NM_018358.2 ./. c.-4123C>T r.(=) p.(=)