Variant #0008018382 (NC_000012.11:g.53701444C>T, NM_021640.3:c.*511C>T (C12orf10))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.53701444C>T
DB-ID -
dbSNP ID rs146223674
gnomAD frequency 1/245744
gnomAD homozygote count 0/122870
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     
AAAS NM_001173466.1 ./. c.1371delGinsA r.(?) p.(Gln457=)
AAAS NM_015665.5 ./. c.1470delGinsA r.(?) p.(Gln490=)
C12orf10 NM_021640.3 ./. c.*511C>T r.(=) p.(=)