List of variants reported as uncertain significance for GTP cyclohydrolase I deficiency with hyperphenylalaninemia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000161.3(GCH1):c.*1628A>C	rs185031007	0.00106
NM_000161.3(GCH1):c.*1033C>T	rs867220379	0.00015
NM_000161.3(GCH1):c.-56G>A	rs866010535	0.00013
NM_000161.3(GCH1):c.328C>G (p.Gln110Glu)	rs748944982	0.00009
NM_000161.3(GCH1):c.*34C>T	rs757193609	0.00002
NM_000161.3(GCH1):c.299C>T (p.Ser100Leu)	rs527416949	0.00002
NM_000161.3(GCH1):c.16G>T (p.Val6Leu)	rs1413964407
NM_000161.3(GCH1):c.514G>A (p.Val172Ile)	rs1566660315
NM_000317.3(PTS):c.91C>A (p.Leu31Ile)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.