Variant #0001325209 (NC_000002.11:g.41619G>A, NM_001077710.2:c.955C>T (FAM110C))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.41619G>A
DB-ID -
dbSNP ID rs776805931
gnomAD frequency 1/245418
gnomAD homozygote count 0/122706
Average frequency (gnomAD v.2.1.1) 0 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FAM110C NM_001077710.2 ./. c.955C>T r.(?) p.(Pro319Ser)