List of variants in gene MYPN reported by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_032578.4(MYPN):c.2886T>C (p.Val962=)	rs10733838	0.98443
NM_032578.4(MYPN):c.2703+17T>C	rs6480306	0.98057
NM_032578.4(MYPN):c.2925+9G>C	rs12241644	0.01362
NM_032578.4(MYPN):c.1245+20A>G	rs111634581	0.00919
NM_032578.4(MYPN):c.1134C>T (p.Ile378=)	rs145701607	0.00504
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu)	rs71534278	0.00318
NM_032578.4(MYPN):c.1893G>A (p.Arg631=)	rs145440469	0.00198
NM_032578.4(MYPN):c.1246-19G>A	rs75739924	0.00157
NM_032578.4(MYPN):c.1104C>T (p.Gly368=)	rs144764983	0.00154
NM_032578.4(MYPN):c.3792C>T (p.Tyr1264=)	rs142307556	0.00100
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.1293C>A (p.Ile431=)	rs147184158	0.00081
NM_032578.4(MYPN):c.1236C>A (p.Thr412=)	rs151220474	0.00058
NM_032578.4(MYPN):c.1935C>T (p.Pro645=)	rs71535754	0.00056
NM_032578.4(MYPN):c.1662A>C (p.Ala554=)	rs71584488	0.00037
NM_032578.4(MYPN):c.3124C>T (p.Arg1042Cys)	rs151282801	0.00034
NM_032578.4(MYPN):c.251A>G (p.Asn84Ser)	rs768968410	0.00010
NM_032578.4(MYPN):c.259C>G (p.Pro87Ala)	rs376945733	0.00010
NM_032578.4(MYPN):c.2864G>A (p.Arg955Gln)	rs199476414	0.00010
NM_032578.4(MYPN):c.1725A>G (p.Lys575=)	rs143213775	0.00009
NM_032578.4(MYPN):c.1466G>A (p.Arg489Gln)	rs141031460	0.00006
NM_032578.4(MYPN):c.3720C>T (p.Asp1240=)	rs146280945	0.00004
NM_032578.4(MYPN):c.3711G>A (p.Lys1237=)	rs773992843	0.00002
NM_032578.4(MYPN):c.3405A>T (p.Pro1135=)	rs1214537721	0.00001
NM_032578.4(MYPN):c.3853G>A (p.Gly1285Arg)	rs750277122	0.00001
NM_032578.4(MYPN):c.2540G>A (p.Gly847Glu)	rs181848049
NM_032578.4(MYPN):c.2726A>C (p.Glu909Ala)	rs1554849161
NM_032578.4(MYPN):c.3493+15_3493+20del	rs11279655
NM_032578.4(MYPN):c.3721G>A (p.Ala1241Thr)	rs1340955437
NM_032578.4(MYPN):c.3735G>T (p.Thr1245=)	rs184347775

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.