Variant #0001325280 (NC_000002.11:g.45564C>T, NM_001077710.2:c.822G>A (FAM110C))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.45564C>T
DB-ID -
dbSNP ID rs374246797
gnomAD frequency 8/245596
gnomAD homozygote count 0/122790
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
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     
FAM110C NM_001077710.2 ./. c.822G>A r.(?) p.(Glu274=)