List of variants in gene GAMT reported by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000156.6(GAMT):c.327G>A (p.Lys109=)	rs80338735	0.00017
NM_000156.6(GAMT):c.522G>A (p.Trp174Ter)	rs370421531	0.00003
NM_000156.6(GAMT):c.391+15G>T	rs367567416	0.00001
NM_000156.6(GAMT):c.467C>A (p.Ala156Asp)	rs368221789	0.00001
NC_000019.9:g.(?_1397025)_1397484del
NM_000156.6(GAMT):c.268G>A (p.Glu90Lys)	rs1569006974
NM_000156.6(GAMT):c.299_311dup (p.Arg105fs)	rs80338736
NM_000156.6(GAMT):c.316C>T (p.Gln106Ter)	rs1369786965
NM_000156.6(GAMT):c.392-2A>G	rs2082618808
NM_000156.6(GAMT):c.475del (p.Leu159fs)
NM_000156.6(GAMT):c.491G>A (p.Gly164Asp)	rs760101382
NM_000156.6(GAMT):c.491del (p.Gly164fs)	rs749390953
NM_000156.6(GAMT):c.491dup (p.Val165fs)	rs749390953
NM_000156.6(GAMT):c.505T>C (p.Cys169Arg)	rs1600158346
NM_000156.6(GAMT):c.521G>A (p.Trp174Ter)	rs200444143
NM_000156.6(GAMT):c.577C>T (p.Gln193Ter)
NM_000156.6(GAMT):c.578A>G (p.Gln193Arg)	rs2082607477

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.