List of variants in gene MYPN reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.2410G>A (p.Gly804Arg)	rs62620248	0.01839
NM_032578.4(MYPN):c.2925+9G>C	rs12241644	0.01362
NM_032578.4(MYPN):c.3279C>T (p.Asp1093=)	rs115033934	0.01152
NM_032578.4(MYPN):c.2447C>T (p.Pro816Leu)	rs111965755	0.01059
NM_032578.4(MYPN):c.1245+20A>G	rs111634581	0.00919
NM_032578.4(MYPN):c.3493+11C>T	rs113674647	0.00520
NM_032578.4(MYPN):c.1134C>T (p.Ile378=)	rs145701607	0.00504
NM_032578.4(MYPN):c.3078G>A (p.Gly1026=)	rs114479328	0.00385
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu)	rs71534278	0.00318
NM_032578.4(MYPN):c.1079-18T>C	rs114932559	0.00278
NM_032578.4(MYPN):c.2236A>G (p.Thr746Ala)	rs147287437	0.00225
NM_032578.4(MYPN):c.59A>G (p.Tyr20Cys)	rs140148105	0.00130
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile)	rs138313730	0.00123
NM_032578.4(MYPN):c.3792C>T (p.Tyr1264=)	rs142307556	0.00100
NM_032578.4(MYPN):c.2228C>T (p.Pro743Leu)	rs138583865	0.00076
NM_032578.4(MYPN):c.2925+18C>T	rs372714890	0.00063
NM_032578.4(MYPN):c.3833G>A (p.Arg1278Gln)	rs142877365	0.00052
NM_032578.4(MYPN):c.1662A>C (p.Ala554=)	rs71584488	0.00037
NM_032578.4(MYPN):c.3934C>T (p.Arg1312Trp)	rs142354704	0.00012
NM_032578.4(MYPN):c.757G>C (p.Gly253Arg)	rs201983087	0.00008
NM_032578.4(MYPN):c.2925+20A>C	rs200111945	0.00005
NM_032578.4(MYPN):c.1200A>G (p.Gln400=)	rs768030641	0.00002
NM_032578.4(MYPN):c.1245+19A>G	rs773859141	0.00001
NM_032578.4(MYPN):c.2537T>C (p.Met846Thr)	rs1261517918
NM_032578.4(MYPN):c.2565-17G>A	rs1334366122
NM_032578.4(MYPN):c.2863C>T (p.Arg955Trp)	rs149887823

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