Variant #0005363089 (NC_000007.13:g.150922122C>T, NC_000007.13(NM_007189.2):c.155-48G>A (ABCF2))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.150922122C>T
DB-ID -
dbSNP ID rs760789143
gnomAD frequency 3/240018
gnomAD homozygote count 0/120006
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     
ABCF2 NM_005692.4 ./. c.155-48G>A r.(=) p.(=)
ABCF2 NM_007189.2 ./. c.155-48G>A r.(=) p.(=)