ClinVar Miner

List of variants in gene MYPN reported as not provided for not provided

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Total variants: 48
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HGVS dbSNP
NM_001256267.1(MYPN):c.2886= (p.Val962=) rs10733838
NM_032578.3(MYPN):c.1016A>T (p.Tyr339Phe) rs199476404
NM_032578.3(MYPN):c.1104C>T (p.Gly368=) rs144764983
NM_032578.3(MYPN):c.1128T>C (p.Asn376=) rs199476405
NM_032578.3(MYPN):c.1178T>C (p.Val393Ala) rs11596653
NM_032578.3(MYPN):c.1229T>C (p.Val410Ala) rs199476406
NM_032578.3(MYPN):c.1251G>A (p.Gln417=) rs10997948
NM_032578.3(MYPN):c.1399G>A (p.Glu467Lys) rs74143030
NM_032578.3(MYPN):c.1419T>C (p.Thr473=) rs199476407
NM_032578.3(MYPN):c.1585C>T (p.Gln529Ter) rs199476408
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.1831G>A (p.Ala611Thr) rs199476409
NM_032578.3(MYPN):c.1840G>A (p.Glu614Lys) rs143338091
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.1935C>T (p.Pro645=) rs71535754
NM_032578.3(MYPN):c.2072G>A (p.Ser691Asn) rs10997975
NM_032578.3(MYPN):c.2072G>C (p.Ser691Thr) 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.2190G>A (p.Thr730=) rs71584492
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.248del (p.Ile83fs) rs71578989
NM_032578.3(MYPN):c.2521C>A (p.Pro841Thr) rs199476410
NM_032578.3(MYPN):c.2642A>T (p.Asn881Ile) rs71584493
NM_032578.3(MYPN):c.2644G>A (p.Ala882Thr) rs199476411
NM_032578.3(MYPN):c.2653C>T (p.Arg885Ter) rs199476412
NM_032578.3(MYPN):c.2862C>A (p.Phe954Leu) rs199476413
NM_032578.3(MYPN):c.2864G>A (p.Arg955Gln) rs199476414
NM_032578.3(MYPN):c.3219A>G (p.Pro1073=) rs199476415
NM_032578.3(MYPN):c.3263G>A (p.Arg1088His) rs71584501
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.3417C>A (p.Arg1139=) rs144488384
NM_032578.3(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730
NM_032578.3(MYPN):c.3583G>A (p.Val1195Met) rs71534280
NM_032578.3(MYPN):c.3793G>C (p.Ala1265Pro) rs199476416
NM_032578.3(MYPN):c.3917T>G (p.Val1306Gly) rs199476417
NM_032578.3(MYPN):c.420T>C (p.Tyr140=) rs71578990
NM_032578.3(MYPN):c.458A>G (p.Lys153Arg) rs199476401
NM_032578.3(MYPN):c.465C>G (p.Ala155=) rs142867001
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.650C>A (p.Ala217Glu) rs199476403
NM_032578.3(MYPN):c.843A>G (p.Pro281=) rs74143022

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