Variant #0005363115 (NC_000007.13:g.150923436G>C, NM_007189.2:c.109C>G (ABCF2))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.150923436G>C
DB-ID -
dbSNP ID rs747907817
gnomAD frequency 2/246186
gnomAD homozygote count 0/123091
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.109C>G r.(?) p.(Pro37Ala)
ABCF2 NM_007189.2 ./. c.109C>G r.(?) p.(Pro37Ala)