List of variants in gene MYPN reported as uncertain significance by ClinVar Staff, National Center for Biotechnology Information (NCBI)

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile)	rs138313730	0.00123
NM_032578.4(MYPN):c.1229T>C (p.Val410Ala)	rs199476406	0.00004
NM_032578.4(MYPN):c.2644G>A (p.Ala882Thr)	rs199476411	0.00003
NM_032578.4(MYPN):c.458A>G (p.Lys153Arg)	rs199476401	0.00002
NM_032578.4(MYPN):c.1016A>T (p.Tyr339Phe)	rs199476404
NM_032578.4(MYPN):c.1831G>A (p.Ala611Thr)	rs199476409
NM_032578.4(MYPN):c.2521C>A (p.Pro841Thr)	rs199476410
NM_032578.4(MYPN):c.2862C>A (p.Phe954Leu)	rs199476413
NM_032578.4(MYPN):c.2863C>T (p.Arg955Trp)	rs149887823
NM_032578.4(MYPN):c.2882C>T (p.Pro961Leu)	rs864621995
NM_032578.4(MYPN):c.3793G>C (p.Ala1265Pro)	rs199476416
NM_032578.4(MYPN):c.637A>G (p.Ile213Val)	rs199476402
NM_032578.4(MYPN):c.650C>A (p.Ala217Glu)	rs199476403

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