ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 18
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NM_032578.3(MYPN):c.1104C>T (p.Gly368=) rs144764983
NM_032578.3(MYPN):c.1134C>T (p.Ile378=) rs145701607
NM_032578.3(MYPN):c.1236C>A (p.Thr412=) rs151220474
NM_032578.3(MYPN):c.1245+20A>G rs111634581
NM_032578.3(MYPN):c.1246-19G>A rs75739924
NM_032578.3(MYPN):c.1293C>A (p.Ile431=) rs147184158
NM_032578.3(MYPN):c.1460-14T>A rs201156035
NM_032578.3(MYPN):c.1662A>C (p.Ala554=) rs71584488
NM_032578.3(MYPN):c.1725A>G (p.Lys575=) rs143213775
NM_032578.3(MYPN):c.1893G>A (p.Arg631=) rs145440469
NM_032578.3(MYPN):c.1935C>T (p.Pro645=) rs71535754
NM_032578.3(MYPN):c.2880T>G (p.Ser960=) rs146028308
NM_032578.3(MYPN):c.2925+9G>C rs12241644
NM_032578.3(MYPN):c.3075+20C>T rs377273417
NM_032578.3(MYPN):c.3720C>T (p.Asp1240=) rs146280945
NM_032578.3(MYPN):c.3735G>T (p.Thr1245=) rs184347775
NM_032578.3(MYPN):c.3792C>T (p.Tyr1264=) rs142307556
NM_032578.3(MYPN):c.395C>T (p.Pro132Leu) rs201203517

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