Variant #0004765276 (NC_000007.13:g.193550C>T, NM_020223.3:c.351C>T (FAM20C))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.193550C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/101554
gnomAD homozygote count 0/50775
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     
FAM20C NM_020223.3 ./. c.351C>T r.(?) p.(Ala117=)