ClinVar Miner

List of variants in gene MYPN reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 88
Download table as spreadsheet
HGVS dbSNP
NM_032578.3(MYPN):c.105G>A (p.Ala35=) rs533632772
NM_032578.3(MYPN):c.1089T>C (p.Ser363=) rs1589553096
NM_032578.3(MYPN):c.1246-6T>C rs767717878
NM_032578.3(MYPN):c.1548T>G (p.Thr516=) rs1589577257
NM_032578.3(MYPN):c.1806G>A (p.Leu602=) rs754999743
NM_032578.3(MYPN):c.1839C>G (p.Ser613=) rs140063470
NM_032578.3(MYPN):c.1839C>T (p.Ser613=) rs140063470
NM_032578.3(MYPN):c.1932C>A (p.Ser644=) rs187664226
NM_032578.3(MYPN):c.1938G>A (p.Val646=) rs776043765
NM_032578.3(MYPN):c.1973+10A>T rs756078237
NM_032578.3(MYPN):c.1974T>C (p.Leu658=) rs1049142458
NM_032578.3(MYPN):c.2093A>G (p.Asn698Ser) rs181355189
NM_032578.3(MYPN):c.2565-7C>T rs373241021
NM_032578.3(MYPN):c.2704-5G>C rs1589602611
NM_032578.3(MYPN):c.2704-7T>G rs1589602602
NM_032578.3(MYPN):c.2709C>T (p.Tyr903=) rs772657844
NM_032578.3(MYPN):c.2742T>C (p.Asn914=) rs372375235
NM_032578.3(MYPN):c.2988A>G (p.Arg996=) rs1589607174
NM_032578.3(MYPN):c.3006C>T (p.Cys1002=) rs1321971649
NM_032578.3(MYPN):c.3039C>T (p.Asp1013=) rs748080770
NM_032578.3(MYPN):c.3075+5_3075+13del rs864622652
NM_032578.3(MYPN):c.3075+9G>A rs370764417
NM_032578.3(MYPN):c.3354C>G (p.Ser1118=) rs1589611936
NM_032578.3(MYPN):c.336T>C (p.Ser112=) rs769858127
NM_032578.3(MYPN):c.339T>C (p.Phe113=) rs773471286
NM_032578.3(MYPN):c.3441C>T (p.Ile1147=) rs759420426
NM_032578.3(MYPN):c.3494-6G>T rs768274852
NM_032578.3(MYPN):c.3552C>G (p.Pro1184=) rs749396604
NM_032578.3(MYPN):c.3567G>A (p.Val1189=) rs1308500781
NM_032578.3(MYPN):c.3612C>T (p.Tyr1204=) rs1457583142
NM_032578.3(MYPN):c.3756C>T (p.Ala1252=) rs765512505
NM_032578.3(MYPN):c.489C>T (p.Ser163=) rs1277548524
NM_032578.3(MYPN):c.528T>C (p.Arg176=) rs1158680867
NM_032578.3(MYPN):c.591C>T (p.Ser197=) rs374950923
NM_032578.3(MYPN):c.741T>G (p.Gly247=) rs1589529211
NM_032578.3(MYPN):c.756A>C (p.Pro252=) rs771623542
NM_032578.4(MYPN):c.1130G>A (p.Arg377Gln) rs147596628
NM_032578.4(MYPN):c.1200A>G (p.Gln400=) rs768030641
NM_032578.4(MYPN):c.1293C>A (p.Ile431=) rs147184158
NM_032578.4(MYPN):c.1335A>T (p.Ser445=) rs1554844105
NM_032578.4(MYPN):c.1536C>T (p.Cys512=) rs569718340
NM_032578.4(MYPN):c.1593C>T (p.His531=) rs138354021
NM_032578.4(MYPN):c.1662A>C (p.Ala554=) rs71584488
NM_032578.4(MYPN):c.1725A>G (p.Lys575=) rs143213775
NM_032578.4(MYPN):c.1851G>A (p.Val617=) rs751087472
NM_032578.4(MYPN):c.1875C>G (p.Pro625=) rs2673793
NM_032578.4(MYPN):c.1899C>T (p.Asn633=) rs147500426
NM_032578.4(MYPN):c.1900G>A (p.Gly634Arg) rs148407539
NM_032578.4(MYPN):c.1944G>A (p.Glu648=) rs151017803
NM_032578.4(MYPN):c.2169G>A (p.Pro723=) rs149357638
NM_032578.4(MYPN):c.2190G>A (p.Thr730=) rs71584492
NM_032578.4(MYPN):c.2228C>T (p.Pro743Leu) rs138583865
NM_032578.4(MYPN):c.2229G>A (p.Pro743=) rs148360410
NM_032578.4(MYPN):c.2260A>C (p.Ile754Leu) rs201245117
NM_032578.4(MYPN):c.2409C>A (p.Ser803Arg) rs3814182
NM_032578.4(MYPN):c.2550A>G (p.Arg850=) rs886039109
NM_032578.4(MYPN):c.2733G>A (p.Arg911=) rs1060504954
NM_032578.4(MYPN):c.2976C>T (p.Cys992=) rs768202837
NM_032578.4(MYPN):c.2986C>A (p.Arg996=) rs753094063
NM_032578.4(MYPN):c.3124C>T (p.Arg1042Cys) rs151282801
NM_032578.4(MYPN):c.3156C>T (p.His1052=) rs876657923
NM_032578.4(MYPN):c.3167C>T (p.Ser1056Phe) rs373101027
NM_032578.4(MYPN):c.3228G>T (p.Leu1076=) rs746111226
NM_032578.4(MYPN):c.3300G>A (p.Pro1100=) rs777293049
NM_032578.4(MYPN):c.3306G>T (p.Pro1102=) rs771521427
NM_032578.4(MYPN):c.3417C>T (p.Arg1139=) rs144488384
NM_032578.4(MYPN):c.3420C>T (p.Asp1140=) rs200786762
NM_032578.4(MYPN):c.3504G>A (p.Val1168=) rs755327022
NM_032578.4(MYPN):c.3552C>T (p.Pro1184=) rs749396604
NM_032578.4(MYPN):c.3576G>A (p.Glu1192=) rs1487958900
NM_032578.4(MYPN):c.3582C>T (p.Arg1194=) rs139820597
NM_032578.4(MYPN):c.3583G>A (p.Val1195Met) rs71534280
NM_032578.4(MYPN):c.3591C>A (p.Gly1197=) rs876657538
NM_032578.4(MYPN):c.3720C>T (p.Asp1240=) rs146280945
NM_032578.4(MYPN):c.3792C>T (p.Tyr1264=) rs142307556
NM_032578.4(MYPN):c.3813C>A (p.Ile1271=) rs777067913
NM_032578.4(MYPN):c.3886T>A (p.Ser1296Thr) rs199585352
NM_032578.4(MYPN):c.392G>T (p.Ser131Ile) rs199853307
NM_032578.4(MYPN):c.3934C>T (p.Arg1312Trp) rs142354704
NM_032578.4(MYPN):c.395C>T (p.Pro132Leu) rs201203517
NM_032578.4(MYPN):c.420T>C (p.Tyr140=) rs71578990
NM_032578.4(MYPN):c.519T>C (p.Ile173=) rs769771296
NM_032578.4(MYPN):c.597C>T (p.Phe199=) rs778049757
NM_032578.4(MYPN):c.59A>G (p.Tyr20Cys) rs140148105
NM_032578.4(MYPN):c.65C>G (p.Ala22Gly) rs145142157
NM_032578.4(MYPN):c.734C>G (p.Ala245Gly) rs143574079
NM_032578.4(MYPN):c.744A>G (p.Gly248=) rs749058723
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.