Variant #0001325240 (NC_000002.11:g.45422A>T, NC_000002.11(NM_001077710.2):c.946+18T>A (FAM110C))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.45422A>T
DB-ID -
dbSNP ID rs377374736
gnomAD frequency 3/228624
gnomAD homozygote count 0/114304
Average frequency (gnomAD v.2.1.1) 1.0E-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.946+18T>A r.(=) p.(=)