Variant #0000311172 (NC_000001.10:g.33790423C>T, NM_198040.2:c.*43G>A (PHC2))

Chromosome 1
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.33790423C>T
DB-ID -
dbSNP ID rs376969728
gnomAD frequency 12/228268
gnomAD homozygote count 0/114107
Average frequency (gnomAD v.2.1.1) 5.0E-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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A3GALT2 NM_001080438.1 ./. c.-3724G>A r.(=) p.(=)
PHC2 NM_004427.3 ./. c.*43G>A r.(=) p.(=)
PHC2 NM_198040.2 ./. c.*43G>A r.(=) p.(=)