ClinVar Miner

List of variants in gene MYPN reported as likely benign for not specified

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Gene type:
ClinVar version:
Total variants: 72
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HGVS dbSNP
NM_032578.3(MYPN):c.*5G>A rs1057522837
NM_032578.3(MYPN):c.-49G>A rs1161034292
NM_032578.3(MYPN):c.1188A>G (p.Pro396=) rs371437119
NM_032578.3(MYPN):c.1236C>T (p.Thr412=) rs151220474
NM_032578.3(MYPN):c.1246-16G>T rs778467080
NM_032578.3(MYPN):c.1293C>A (p.Ile431=) rs147184158
NM_032578.3(MYPN):c.1317+7A>C rs751723015
NM_032578.3(MYPN):c.1431T>C (p.Asp477=) rs1464264584
NM_032578.3(MYPN):c.1460-14T>A rs201156035
NM_032578.3(MYPN):c.1483+11T>C rs765156367
NM_032578.3(MYPN):c.1536C>T (p.Cys512=) rs569718340
NM_032578.3(MYPN):c.1563C>T (p.Tyr521=) rs77249928
NM_032578.3(MYPN):c.1623C>T (p.Asn541=) rs746849244
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.1790G>A (p.Arg597His) rs150911078
NM_032578.3(MYPN):c.1851G>A (p.Val617=) rs751087472
NM_032578.3(MYPN):c.1863A>G (p.Arg621=) rs373826163
NM_032578.3(MYPN):c.1890G>A (p.Glu630=) rs201960380
NM_032578.3(MYPN):c.1892G>A (p.Arg631Lys) rs1057520698
NM_032578.3(MYPN):c.1935C>T (p.Pro645=) rs71535754
NM_032578.3(MYPN):c.1952C>A (p.Pro651Gln) rs548318517
NM_032578.3(MYPN):c.1973+11A>G rs763753325
NM_032578.3(MYPN):c.1973+13T>C rs753685932
NM_032578.3(MYPN):c.2028A>G (p.Gln676=) rs876657537
NM_032578.3(MYPN):c.2151G>A (p.Thr717=) rs150223120
NM_032578.3(MYPN):c.2169G>T (p.Pro723=) rs149357638
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.2229G>A (p.Pro743=) rs148360410
NM_032578.3(MYPN):c.2229G>C (p.Pro743=) rs148360410
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.2466G>A (p.Arg822=) rs1298116965
NM_032578.3(MYPN):c.2703+13G>A rs375320760
NM_032578.3(MYPN):c.2703+20_2703+22delAAG rs1064795919
NM_032578.3(MYPN):c.2736G>A (p.Leu912=) rs1057523127
NM_032578.3(MYPN):c.282T>C (p.Thr94=) rs371623282
NM_032578.3(MYPN):c.2880T>G (p.Ser960=) rs146028308
NM_032578.3(MYPN):c.2925+18C>T rs372714890
NM_032578.3(MYPN):c.2949G>A (p.Lys983=) rs375015526
NM_032578.3(MYPN):c.3075+20C>T rs377273417
NM_032578.3(MYPN):c.3122T>A (p.Ile1041Asn) rs754227127
NM_032578.3(MYPN):c.312G>A (p.Gln104=) rs571241816
NM_032578.3(MYPN):c.3228G>T (p.Leu1076=) rs746111226
NM_032578.3(MYPN):c.3285+15C>T rs1554850514
NM_032578.3(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278
NM_032578.3(MYPN):c.3416G>A (p.Arg1139His) rs531222847
NM_032578.3(MYPN):c.3417C>G (p.Arg1139=) rs144488384
NM_032578.3(MYPN):c.3417C>T (p.Arg1139=) rs144488384
NM_032578.3(MYPN):c.3493+6G>A rs750903219
NM_032578.3(MYPN):c.3493+6G>C rs750903219
NM_032578.3(MYPN):c.3552C>T (p.Pro1184=) rs749396604
NM_032578.3(MYPN):c.3582C>T (p.Arg1194=) rs139820597
NM_032578.3(MYPN):c.3591C>A (p.Gly1197=) rs876657538
NM_032578.3(MYPN):c.360T>A (p.Asp120Glu) rs794729068
NM_032578.3(MYPN):c.3768G>A (p.Ser1256=) rs533708375
NM_032578.3(MYPN):c.3813C>A (p.Ile1271=) rs777067913
NM_032578.3(MYPN):c.3846T>A (p.Ser1282Arg) rs147659164
NM_032578.3(MYPN):c.395C>T (p.Pro132Leu) rs201203517
NM_032578.3(MYPN):c.39T>C (p.Ser13=) rs1554839150
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.65C>G (p.Ala22Gly) rs145142157
NM_032578.3(MYPN):c.660G>A (p.Arg220=) rs372218308
NM_032578.3(MYPN):c.714G>A (p.Ala238=) rs757661676
NM_032578.3(MYPN):c.734C>G (p.Ala245Gly) rs143574079
NM_032578.3(MYPN):c.902+15T>C rs1341748670
NM_032578.3(MYPN):c.948C>T (p.His316=) rs200674758
NM_032578.3(MYPN):c.951C>A (p.Ile317=) rs759998419
NM_032578.3(MYPN):c.951C>T (p.Ile317=) rs759998419
NM_032578.3(MYPN):c.952G>A (p.Val318Ile) rs112518450

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