Variant #0003420228 (NC_000004.11:g.146018617A>G, NM_001040876.1:c.-979A>G (ABCE1))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.146018617A>G
DB-ID -
dbSNP ID rs779785171
gnomAD frequency 11/123114
gnomAD homozygote count 0/61546
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     
ABCE1 NM_001040876.1 ./. c.-979A>G r.(=) p.(=)
ANAPC10 NM_001256706.1 ./. c.-13+655T>C r.(=) p.(=)
ANAPC10 NM_001256707.1 ./. c.-13+223T>C r.(=) p.(=)
ANAPC10 NM_001256708.1 ./. c.-13+771T>C r.(=) p.(=)
ANAPC10 NM_001256709.1 ./. c.21+30T>C r.(=) p.(=)
ANAPC10 NM_001256710.1 ./. c.-13+655T>C r.(=) p.(=)
ANAPC10 NM_001256711.1 ./. c.-13+223T>C r.(=) p.(=)
ANAPC10 NM_001256712.1 ./. c.-13+666T>C r.(=) p.(=)
ABCE1 NM_002940.2 ./. c.-982A>G r.(=) p.(=)
ANAPC10 NM_014885.4 ./. c.-13+666T>C r.(=) p.(=)