ClinVar Miner

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

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Gene type:
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Total variants: 69
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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.1130G>A (p.Arg377Gln) rs147596628
NM_032578.3(MYPN):c.1132A>C (p.Ile378Leu) rs1554842686
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.1188A>G (p.Pro396=) rs371437119
NM_032578.3(MYPN):c.1225C>T (p.Arg409Cys) rs757431496
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.1460-14T>A rs201156035
NM_032578.3(MYPN):c.1536C>T (p.Cys512=) rs569718340
NM_032578.3(MYPN):c.1647T>C (p.Ser549=) rs2673794
NM_032578.3(MYPN):c.1662A>C (p.Ala554=) rs71584488
NM_032578.3(MYPN):c.1741G>C (p.Val581Leu) rs1464184643
NM_032578.3(MYPN):c.1757A>G (p.Asn586Ser) rs550455783
NM_032578.3(MYPN):c.1790G>A (p.Arg597His) rs150911078
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.1935C>T (p.Pro645=) rs71535754
NM_032578.3(MYPN):c.2028A>G (p.Gln676=) rs876657537
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.2134G>C (p.Ala712Pro) rs876657921
NM_032578.3(MYPN):c.2163C>A (p.Ala721=) rs71584491
NM_032578.3(MYPN):c.2190G>A (p.Thr730=) rs71584492
NM_032578.3(MYPN):c.2228C>T (p.Pro743Leu) rs138583865
NM_032578.3(MYPN):c.2236A>G (p.Thr746Ala) rs147287437
NM_032578.3(MYPN):c.2260A>C (p.Ile754Leu) rs201245117
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.2443A>G (p.Ile815Val) rs876657922
NM_032578.3(MYPN):c.2447C>T (p.Pro816Leu) rs111965755
NM_032578.3(MYPN):c.2466G>A (p.Arg822=) rs1298116965
NM_032578.3(MYPN):c.2507C>T (p.Ser836Phe)
NM_032578.3(MYPN):c.2703+13G>A rs375320760
NM_032578.3(MYPN):c.2863C>T (p.Arg955Trp) rs149887823
NM_032578.3(MYPN):c.2880T>G (p.Ser960=) rs146028308
NM_032578.3(MYPN):c.2925+9G>C rs12241644
NM_032578.3(MYPN):c.3078G>A (p.Gly1026=) rs114479328
NM_032578.3(MYPN):c.3156C>T (p.His1052=) rs876657923
NM_032578.3(MYPN):c.3279C>T (p.Asp1093=) rs115033934
NM_032578.3(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278
NM_032578.3(MYPN):c.3403C>A (p.Pro1135Thr) rs7079481
NM_032578.3(MYPN):c.3416G>A (p.Arg1139His) rs531222847
NM_032578.3(MYPN):c.3417C>T (p.Arg1139=) rs144488384
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.3582C>T (p.Arg1194=) rs139820597
NM_032578.3(MYPN):c.3583G>A (p.Val1195Met) rs71534280
NM_032578.3(MYPN):c.3591C>A (p.Gly1197=) rs876657538
NM_032578.3(MYPN):c.3763G>A (p.Val1255Met) rs750655311
NM_032578.3(MYPN):c.3768G>A (p.Ser1256=) rs533708375
NM_032578.3(MYPN):c.3833G>A (p.Arg1278Gln) rs142877365
NM_032578.3(MYPN):c.3846T>A (p.Ser1282Arg) rs147659164
NM_032578.3(MYPN):c.465C>G (p.Ala155=) rs142867001
NM_032578.3(MYPN):c.54G>C (p.Glu18Asp) rs876657919
NM_032578.3(MYPN):c.59A>G (p.Tyr20Cys) rs140148105
NM_032578.3(MYPN):c.637A>G (p.Ile213Val) rs199476402
NM_032578.3(MYPN):c.65C>G (p.Ala22Gly) rs145142157
NM_032578.3(MYPN):c.734C>G (p.Ala245Gly) rs143574079
NM_032578.3(MYPN):c.785A>G (p.Glu262Gly) rs876657924
NM_032578.3(MYPN):c.80G>C (p.Arg27Pro) rs529359915
NM_032578.3(MYPN):c.843A>G (p.Pro281=) rs74143022
NM_032578.3(MYPN):c.935C>T (p.Ser312Phe) rs786205457

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