List of variants in gene MCM3AP reported by Mayo Clinic Laboratories, Mayo Clinic

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_003906.5(MCM3AP):c.1267A>G (p.Thr423Ala)	rs144151494	0.00162
NM_003906.5(MCM3AP):c.1592A>G (p.Glu531Gly)	rs144333393	0.00025
NM_003906.5(MCM3AP):c.5276C>T (p.Pro1759Leu)	rs201207310	0.00021
NM_003906.5(MCM3AP):c.1049A>T (p.Lys350Met)	rs147565274	0.00010
NM_003906.5(MCM3AP):c.4319C>T (p.Ala1440Val)	rs771441002	0.00006
NM_003906.5(MCM3AP):c.5831C>T (p.Thr1944Met)	rs141098252	0.00005
NM_003906.5(MCM3AP):c.3188A>G (p.Gln1063Arg)	rs750855467	0.00004
NM_003906.5(MCM3AP):c.343C>T (p.Pro115Ser)	rs138351858	0.00004
NM_003906.5(MCM3AP):c.2998G>A (p.Val1000Ile)	rs779913783	0.00003
NM_003906.5(MCM3AP):c.1443+4A>G	rs771048180	0.00001
NM_003906.5(MCM3AP):c.5828G>A (p.Gly1943Glu)	rs767783662	0.00001
NM_003906.5(MCM3AP):c.3061G>A (p.Glu1021Lys)
NM_003906.5(MCM3AP):c.3782G>T (p.Arg1261Leu)	rs150680624
NM_003906.5(MCM3AP):c.4301G>A (p.Gly1434Asp)
NM_003906.5(MCM3AP):c.4433C>T (p.Ser1478Leu)

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