ClinVar Miner

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

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Gene type:
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Total variants: 37
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HGVS dbSNP
NM_001256267.1(MYPN):c.3124C>T (p.Arg1042Cys) rs151282801
NM_001256267.1(MYPN):c.3886T>A (p.Ser1296Thr) rs199585352
NM_032578.3(MYPN):c.1130G>A (p.Arg377Gln) rs147596628
NM_032578.3(MYPN):c.1200A>G (p.Gln400=) rs768030641
NM_032578.3(MYPN):c.1293C>A (p.Ile431=) rs147184158
NM_032578.3(MYPN):c.1335A>T (p.Ser445=) rs1554844105
NM_032578.3(MYPN):c.1536C>T (p.Cys512=) rs569718340
NM_032578.3(MYPN):c.1593C>T (p.His531=) rs138354021
NM_032578.3(MYPN):c.1662A>C (p.Ala554=) rs71584488
NM_032578.3(MYPN):c.1851G>A (p.Val617=) rs751087472
NM_032578.3(MYPN):c.1900G>A (p.Gly634Arg) rs148407539
NM_032578.3(MYPN):c.1944G>A (p.Glu648=) rs151017803
NM_032578.3(MYPN):c.2169G>A (p.Pro723=) rs149357638
NM_032578.3(MYPN):c.2229G>A (p.Pro743=) rs148360410
NM_032578.3(MYPN):c.2260A>C (p.Ile754Leu) rs201245117
NM_032578.3(MYPN):c.2409C>A (p.Ser803Arg) rs3814182
NM_032578.3(MYPN):c.2733G>A (p.Arg911=) rs1060504954
NM_032578.3(MYPN):c.2976C>T (p.Cys992=) rs768202837
NM_032578.3(MYPN):c.2986C>A (p.Arg996=) rs753094063
NM_032578.3(MYPN):c.3075+5_3075+13delAGACGCAGG rs864622652
NM_032578.3(MYPN):c.3300G>A (p.Pro1100=) rs777293049
NM_032578.3(MYPN):c.3417C>T (p.Arg1139=) rs144488384
NM_032578.3(MYPN):c.3420C>T (p.Asp1140=) rs200786762
NM_032578.3(MYPN):c.3576G>A (p.Glu1192=) rs1487958900
NM_032578.3(MYPN):c.3582C>T (p.Arg1194=) rs139820597
NM_032578.3(MYPN):c.3720C>T (p.Asp1240=) rs146280945
NM_032578.3(MYPN):c.3792C>T (p.Tyr1264=) rs142307556
NM_032578.3(MYPN):c.3813C>A (p.Ile1271=) rs777067913
NM_032578.3(MYPN):c.392G>T (p.Ser131Ile) rs199853307
NM_032578.3(MYPN):c.395C>T (p.Pro132Leu) rs201203517
NM_032578.3(MYPN):c.420T>C (p.Tyr140=) rs71578990
NM_032578.3(MYPN):c.519T>C (p.Ile173=) rs769771296
NM_032578.3(MYPN):c.597C>T (p.Phe199=) rs778049757
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.734C>G (p.Ala245Gly) rs143574079
NM_032578.3(MYPN):c.744A>G (p.Gly248=) rs749058723

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