List of variants in gene GAMT reported by Fulgent Genetics, Fulgent Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000156.6(GAMT):c.227C>T (p.Ser76Leu)	rs150338273	0.00036
NM_000156.6(GAMT):c.327G>A (p.Lys109=)	rs80338735	0.00017
NM_000156.6(GAMT):c.511C>G (p.Leu171Val)	rs770110177	0.00005
NM_000156.6(GAMT):c.522G>A (p.Trp174Ter)	rs370421531	0.00003
NM_000156.6(GAMT):c.220G>A (p.Ala74Thr)	rs749284008	0.00002
NM_000156.6(GAMT):c.403G>A (p.Asp135Asn)	rs774144200	0.00002
NM_000156.6(GAMT):c.493G>A (p.Val165Ile)	rs1050914	0.00002
NM_000156.6(GAMT):c.293G>A (p.Arg98Gln)	rs200052696	0.00001
NM_000156.6(GAMT):c.407C>T (p.Thr136Met)	rs374724533	0.00001
NM_000156.6(GAMT):c.473G>A (p.Arg158His)	rs750195151	0.00001
NM_000156.6(GAMT):c.299_311dup (p.Arg105fs)	rs80338736
NM_000156.6(GAMT):c.307del (p.Ala103fs)	rs2082622867
NM_000156.6(GAMT):c.463C>G (p.His155Asp)	rs1374777721
NM_000156.6(GAMT):c.509A>G (p.Asn170Ser)	rs202199674
NM_000156.6(GAMT):c.578A>G (p.Gln193Arg)	rs2082607477
NM_000156.6(GAMT):c.650C>A (p.Pro217Gln)	rs139890971

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