ClinVar Miner

List of variants in gene MYPN reported as benign by Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine

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Gene type:
ClinVar version:
Total variants: 27
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HGVS dbSNP
NM_001256267.1(MYPN):c.2886= (p.Val962=) rs10733838
NM_032578.3(MYPN):c.1104C>T (p.Gly368=) rs144764983
NM_032578.3(MYPN):c.1122G>A (p.Glu374=) rs145103325
NM_032578.3(MYPN):c.1134C>T (p.Ile378=) rs145701607
NM_032578.3(MYPN):c.1178T>C (p.Val393Ala) rs11596653
NM_032578.3(MYPN):c.1251G>A (p.Gln417=) rs10997948
NM_032578.3(MYPN):c.1293C>A (p.Ile431=) rs147184158
NM_032578.3(MYPN):c.1399G>A (p.Glu467Lys) rs74143030
NM_032578.3(MYPN):c.1647T>C (p.Ser549=) rs2673794
NM_032578.3(MYPN):c.1869C>A (p.Thr623=) rs61854624
NM_032578.3(MYPN):c.1875C>T (p.Pro625=) rs2673793
NM_032578.3(MYPN):c.1884C>G (p.Phe628Leu) rs10823148
NM_032578.3(MYPN):c.1893G>A (p.Arg631=) rs145440469
NM_032578.3(MYPN):c.2072G>A (p.Ser691Asn) rs10997975
NM_032578.3(MYPN):c.2120G>A (p.Ser707Asn) rs7916821
NM_032578.3(MYPN):c.2163C>A (p.Ala721=) rs71584491
NM_032578.3(MYPN):c.2409C>G (p.Ser803Arg) rs3814182
NM_032578.3(MYPN):c.2410G>A (p.Gly804Arg) rs62620248
NM_032578.3(MYPN):c.2447C>T (p.Pro816Leu) rs111965755
NM_032578.3(MYPN):c.2925+9G>C rs12241644
NM_032578.3(MYPN):c.3078G>A (p.Gly1026=) rs114479328
NM_032578.3(MYPN):c.3279C>T (p.Asp1093=) rs115033934
NM_032578.3(MYPN):c.3403C>A (p.Pro1135Thr) rs7079481
NM_032578.3(MYPN):c.3421G>A (p.Ala1141Thr) rs150404143
NM_032578.3(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730
NM_032578.3(MYPN):c.3768G>A (p.Ser1256=) rs533708375
NM_032578.3(MYPN):c.843A>G (p.Pro281=) rs74143022

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