List of variants in gene MYPN reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu)	rs71534278	0.00318
NM_032578.4(MYPN):c.2236A>G (p.Thr746Ala)	rs147287437	0.00225
NM_032578.4(MYPN):c.3846T>A (p.Ser1282Arg)	rs147659164	0.00222
NM_032578.4(MYPN):c.1790G>A (p.Arg597His)	rs150911078	0.00158
NM_032578.4(MYPN):c.59A>G (p.Tyr20Cys)	rs140148105	0.00130
NM_032578.4(MYPN):c.465C>G (p.Ala155=)	rs142867001	0.00099
NM_032578.4(MYPN):c.1460-14T>A	rs201156035	0.00096
NM_032578.4(MYPN):c.2880T>G (p.Ser960=)	rs146028308	0.00096
NM_032578.4(MYPN):c.734C>G (p.Ala245Gly)	rs143574079	0.00093
NM_032578.4(MYPN):c.2228C>T (p.Pro743Leu)	rs138583865	0.00076
NM_032578.4(MYPN):c.2703+13G>A	rs375320760	0.00063
NM_032578.4(MYPN):c.1935C>T (p.Pro645=)	rs71535754	0.00056
NM_032578.4(MYPN):c.2190G>A (p.Thr730=)	rs71584492	0.00040
NM_032578.4(MYPN):c.1662A>C (p.Ala554=)	rs71584488	0.00037
NM_032578.4(MYPN):c.2260A>C (p.Ile754Leu)	rs201245117	0.00009
NM_032578.4(MYPN):c.1536C>T (p.Cys512=)	rs569718340	0.00005
NM_032578.4(MYPN):c.3582C>T (p.Arg1194=)	rs139820597	0.00005
NM_032578.4(MYPN):c.3416G>A (p.Arg1139His)	rs531222847	0.00004
NM_032578.4(MYPN):c.3417C>T (p.Arg1139=)	rs144488384	0.00003
NM_032578.4(MYPN):c.3591C>A (p.Gly1197=)	rs876657538	0.00003
NM_032578.4(MYPN):c.1188A>G (p.Pro396=)	rs371437119	0.00001
NM_032578.4(MYPN):c.2466G>A (p.Arg822=)	rs1298116965	0.00001
NM_032578.4(MYPN):c.2028A>G (p.Gln676=)	rs876657537

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