ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 70
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_032578.4(MYPN):c.3403C>A (p.Pro1135Thr) rs7079481 0.40619
NM_032578.4(MYPN):c.1884C>G (p.Phe628Leu) rs10823148 0.39447
NM_032578.4(MYPN):c.2072G>A (p.Ser691Asn) rs10997975 0.39270
NM_032578.4(MYPN):c.2120G>A (p.Ser707Asn) rs7916821 0.39079
NM_032578.4(MYPN):c.2410G>A (p.Gly804Arg) rs62620248 0.01839
NM_032578.4(MYPN):c.2447C>T (p.Pro816Leu) rs111965755 0.01059
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278 0.00318
NM_032578.4(MYPN):c.2236A>G (p.Thr746Ala) rs147287437 0.00225
NM_032578.4(MYPN):c.3846T>A (p.Ser1282Arg) rs147659164 0.00222
NM_032578.4(MYPN):c.1563C>T (p.Tyr521=) rs77249928 0.00189
NM_032578.4(MYPN):c.1790G>A (p.Arg597His) rs150911078 0.00158
NM_032578.4(MYPN):c.59A>G (p.Tyr20Cys) rs140148105 0.00130
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730 0.00123
NM_032578.4(MYPN):c.3792C>T (p.Tyr1264=) rs142307556 0.00100
NM_032578.4(MYPN):c.465C>G (p.Ala155=) rs142867001 0.00099
NM_032578.4(MYPN):c.1460-14T>A rs201156035 0.00096
NM_032578.4(MYPN):c.2880T>G (p.Ser960=) rs146028308 0.00096
NM_032578.4(MYPN):c.734C>G (p.Ala245Gly) rs143574079 0.00093
NM_032578.4(MYPN):c.3583G>A (p.Val1195Met) rs71534280 0.00083
NM_032578.4(MYPN):c.1293C>A (p.Ile431=) rs147184158 0.00081
NM_032578.4(MYPN):c.2228C>T (p.Pro743Leu) rs138583865 0.00076
NM_032578.4(MYPN):c.2703+13G>A rs375320760 0.00063
NM_032578.4(MYPN):c.2925+18C>T rs372714890 0.00063
NM_032578.4(MYPN):c.1935C>T (p.Pro645=) rs71535754 0.00056
NM_032578.4(MYPN):c.2190G>A (p.Thr730=) rs71584492 0.00040
NM_032578.4(MYPN):c.1662A>C (p.Ala554=) rs71584488 0.00037
NM_032578.4(MYPN):c.3124C>T (p.Arg1042Cys) rs151282801 0.00034
NM_032578.4(MYPN):c.2229G>A (p.Pro743=) rs148360410 0.00022
NM_032578.4(MYPN):c.1483+11T>C rs765156367 0.00013
NM_032578.4(MYPN):c.282T>C (p.Thr94=) rs371623282 0.00013
NM_032578.4(MYPN):c.2260A>C (p.Ile754Leu) rs201245117 0.00009
NM_032578.4(MYPN):c.660G>A (p.Arg220=) rs372218308 0.00007
NM_032578.4(MYPN):c.1890G>A (p.Glu630=) rs201960380 0.00006
NM_032578.4(MYPN):c.1536C>T (p.Cys512=) rs569718340 0.00005
NM_032578.4(MYPN):c.3582C>T (p.Arg1194=) rs139820597 0.00005
NM_032578.4(MYPN):c.3416G>A (p.Arg1139His) rs531222847 0.00004
NM_032578.4(MYPN):c.1973+11A>G rs763753325 0.00003
NM_032578.4(MYPN):c.3228G>T (p.Leu1076=) rs746111226 0.00003
NM_032578.4(MYPN):c.3417C>T (p.Arg1139=) rs144488384 0.00003
NM_032578.4(MYPN):c.3552C>T (p.Pro1184=) rs749396604 0.00003
NM_032578.4(MYPN):c.3591C>A (p.Gly1197=) rs876657538 0.00003
NM_032578.4(MYPN):c.714G>A (p.Ala238=) rs757661676 0.00003
NM_032578.4(MYPN):c.-49G>A rs1161034292 0.00002
NM_032578.4(MYPN):c.1317+7A>C rs751723015 0.00002
NM_032578.4(MYPN):c.2151G>A (p.Thr717=) rs150223120 0.00002
NM_032578.4(MYPN):c.3768G>A (p.Ser1256=) rs533708375 0.00002
NM_032578.4(MYPN):c.948C>T (p.His316=) rs200674758 0.00002
NM_032578.4(MYPN):c.1071T>C (p.Tyr357=) rs1323471969 0.00001
NM_032578.4(MYPN):c.1188A>G (p.Pro396=) rs371437119 0.00001
NM_032578.4(MYPN):c.1863A>G (p.Arg621=) rs373826163 0.00001
NM_032578.4(MYPN):c.2466G>A (p.Arg822=) rs1298116965 0.00001
NM_032578.4(MYPN):c.312G>A (p.Gln104=) rs571241816 0.00001
NM_032578.4(MYPN):c.902+15T>C rs1341748670 0.00001
NM_032578.4(MYPN):c.951C>A (p.Ile317=) rs759998419 0.00001
NM_032578.4(MYPN):c.*5G>A rs1057522837
NM_032578.4(MYPN):c.1246-16G>T rs778467080
NM_032578.4(MYPN):c.1973+13T>C rs753685932
NM_032578.4(MYPN):c.2028A>G (p.Gln676=) rs876657537
NM_032578.4(MYPN):c.2169G>T (p.Pro723=) rs149357638
NM_032578.4(MYPN):c.2229G>C (p.Pro743=) rs148360410
NM_032578.4(MYPN):c.2703+17_2703+18delinsCG rs2134205089
NM_032578.4(MYPN):c.2703+20_2703+22del rs1064795919
NM_032578.4(MYPN):c.2736G>A (p.Leu912=) rs1057523127
NM_032578.4(MYPN):c.2949G>A (p.Lys983=) rs375015526
NM_032578.4(MYPN):c.3285+15C>T rs1554850514
NM_032578.4(MYPN):c.3493+6G>A rs750903219
NM_032578.4(MYPN):c.3493+6G>C rs750903219
NM_032578.4(MYPN):c.360T>A (p.Asp120Glu) rs794729068
NM_032578.4(MYPN):c.39T>C (p.Ser13=) rs1554839150
NM_032578.4(MYPN):c.951C>T (p.Ile317=) rs759998419

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.