List of variants in gene MYPN reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 28

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HGVS	dbSNP	gnomAD frequency
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.2236A>G (p.Thr746Ala)	rs147287437	0.00225
NM_032578.4(MYPN):c.1893G>A (p.Arg631=)	rs145440469	0.00198
NM_032578.4(MYPN):c.1563C>T (p.Tyr521=)	rs77249928	0.00189
NM_032578.4(MYPN):c.1104C>T (p.Gly368=)	rs144764983	0.00154
NM_032578.4(MYPN):c.1122G>A (p.Glu374=)	rs145103325	0.00101
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.1293C>A (p.Ile431=)	rs147184158	0.00081
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.1944G>A (p.Glu648=)	rs151017803	0.00041
NM_032578.4(MYPN):c.1662A>C (p.Ala554=)	rs71584488	0.00037
NM_032578.4(MYPN):c.2229G>A (p.Pro743=)	rs148360410	0.00022
NM_032578.4(MYPN):c.259C>G (p.Pro87Ala)	rs376945733	0.00010
NM_032578.4(MYPN):c.1725A>G (p.Lys575=)	rs143213775	0.00009
NM_032578.4(MYPN):c.3456C>T (p.Thr1152=)	rs202183926	0.00005
NM_032578.4(MYPN):c.3720C>T (p.Asp1240=)	rs146280945	0.00004
NM_032578.4(MYPN):c.1899C>T (p.Asn633=)	rs147500426	0.00003
NM_032578.4(MYPN):c.3711G>A (p.Lys1237=)	rs773992843	0.00002
NM_032578.4(MYPN):c.3564C>T (p.Pro1188=)	rs768400415	0.00001
NM_032578.4(MYPN):c.903-18A>T	rs775857947	0.00001
NM_032578.4(MYPN):c.3417C>G (p.Arg1139=)	rs144488384
NM_032578.4(MYPN):c.3493+6G>A	rs750903219
NM_032578.4(MYPN):c.3493+6G>T	rs750903219
NM_032578.4(MYPN):c.3659+8A>G	rs2134311963
NM_032578.4(MYPN):c.465C>A (p.Ala155=)	rs142867001

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