Variant #0004225533 (NC_000006.11:g.30552388C>G, NM_001025091.1:c.1391+45delCinsG (ABCF1))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.30552388C>G
DB-ID -
dbSNP ID rs763279732
gnomAD frequency 5/177698
gnomAD homozygote count 0/88841
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     
ABCF1 NM_001025091.1 ./. c.1391+45delCinsG r.(=) p.(=)
ABCF1 NM_001090.2 ./. c.1277+45delCinsG r.(=) p.(=)