List of variants in gene PLG 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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000301.5(PLG):c.112A>G (p.Lys38Glu)	rs73015965	0.00279
NM_000301.5(PLG):c.782G>A (p.Arg261His)	rs4252187	0.00273
NM_000301.5(PLG):c.2045T>A (p.Ile682Asn)	rs147175166	0.00074
NM_000301.5(PLG):c.514A>G (p.Arg172Gly)	rs145535174	0.00039
NM_000301.5(PLG):c.1499C>T (p.Thr500Met)	rs140970354	0.00022
NM_000301.5(PLG):c.1997T>C (p.Ile666Thr)	rs764647453	0.00010
NM_000301.5(PLG):c.2026G>A (p.Val676Ile)	rs142551860	0.00010
NM_000301.5(PLG):c.115A>C (p.Lys39Gln)	rs138353396	0.00007
NM_000301.5(PLG):c.2271+5G>A	rs746165731	0.00006
NM_000301.5(PLG):c.476C>T (p.Pro159Leu)	rs201792453	0.00005
NM_000301.5(PLG):c.368C>T (p.Thr123Ile)	rs370856655	0.00004
NM_000301.5(PLG):c.1394C>T (p.Pro465Leu)	rs374995543	0.00003
NM_000301.5(PLG):c.1416T>A (p.Asp472Glu)	rs748980932	0.00003
NM_000301.5(PLG):c.1757T>C (p.Val586Ala)	rs1481792306	0.00002
NM_000301.5(PLG):c.17T>C (p.Val6Ala)	rs764121149	0.00002
NM_000301.5(PLG):c.1940C>T (p.Pro647Leu)	rs187157735	0.00001
NM_000301.5(PLG):c.2085C>A (p.Asp695Glu)	rs1394466422	0.00001
NM_000301.5(PLG):c.2347G>A (p.Gly783Ser)	rs915467370	0.00001
NM_000301.5(PLG):c.316G>T (p.Gly106Trp)	rs141284301	0.00001
NM_000301.5(PLG):c.1180A>G (p.Thr394Ala)	rs2484358357
NM_000301.5(PLG):c.1570G>A (p.Ala524Thr)	rs1778005702
NM_000301.5(PLG):c.1657G>A (p.Asp553Asn)	rs182937977
NM_000301.5(PLG):c.1748G>C (p.Gly583Ala)	rs551058645
NM_000301.5(PLG):c.1802+5G>A	rs1778096564
NM_000301.5(PLG):c.2420T>C (p.Met807Thr)	rs773525076
NM_000301.5(PLG):c.293-14G>A	rs773735177
NM_000301.5(PLG):c.426C>A (p.His142Gln)	rs777371711
NM_000301.5(PLG):c.717G>C (p.Arg239Ser)	rs1166718485
NM_000301.5(PLG):c.745G>A (p.Asp249Asn)	rs532027310
NM_000301.5(PLG):c.763del (p.Glu255fs)
NM_000301.5(PLG):c.814A>G (p.Thr272Ala)	rs754598185

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