ClinVar Miner

List of variants in gene MYPN reported as uncertain significance by Ambry Genetics

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Gene type:
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Total variants: 44
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HGVS dbSNP
NM_032578.3(MYPN):c.1109C>T (p.Pro370Leu) rs749986338
NM_032578.3(MYPN):c.1130G>A (p.Arg377Gln) rs147596628
NM_032578.3(MYPN):c.121C>T (p.Pro41Ser) rs759400657
NM_032578.3(MYPN):c.1681T>C (p.Ser561Pro) rs1554845447
NM_032578.3(MYPN):c.1879T>A (p.Ser627Thr) rs1282443178
NM_032578.3(MYPN):c.1900G>A (p.Gly634Arg) rs148407539
NM_032578.3(MYPN):c.2114C>T (p.Thr705Ile) rs768471574
NM_032578.3(MYPN):c.2165G>A (p.Arg722Gln) rs530701227
NM_032578.3(MYPN):c.2183C>T (p.Pro728Leu) rs570682390
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.2644G>A (p.Ala882Thr) rs199476411
NM_032578.3(MYPN):c.2654G>A (p.Arg885Gln) rs370657396
NM_032578.3(MYPN):c.2802T>A (p.His934Gln) rs752426180
NM_032578.3(MYPN):c.2863C>T (p.Arg955Trp) rs149887823
NM_032578.3(MYPN):c.2972A>G (p.His991Arg) rs181021602
NM_032578.3(MYPN):c.3017T>G (p.Ile1006Ser) rs864622711
NM_032578.3(MYPN):c.3040G>A (p.Asp1014Asn) rs769591145
NM_032578.3(MYPN):c.3086G>T (p.Ser1029Ile) rs142320290
NM_032578.3(MYPN):c.3124C>T (p.Arg1042Cys) rs151282801
NM_032578.3(MYPN):c.3146G>A (p.Gly1049Asp) rs878855165
NM_032578.3(MYPN):c.3167C>T (p.Ser1056Phe) rs373101027
NM_032578.3(MYPN):c.3305C>T (p.Pro1102Leu) rs201693405
NM_032578.3(MYPN):c.3544G>A (p.Gly1182Ser) rs777875865
NM_032578.3(MYPN):c.3580C>T (p.Arg1194Cys) rs762310456
NM_032578.3(MYPN):c.3583G>A (p.Val1195Met) rs71534280
NM_032578.3(MYPN):c.3593T>C (p.Met1198Thr) rs755560876
NM_032578.3(MYPN):c.3653G>A (p.Arg1218Lys) rs768630077
NM_032578.3(MYPN):c.3808C>G (p.Gln1270Glu) rs730880169
NM_032578.3(MYPN):c.3833G>A (p.Arg1278Gln) rs142877365
NM_032578.3(MYPN):c.392G>T (p.Ser131Ile) rs199853307
NM_032578.3(MYPN):c.3934C>T (p.Arg1312Trp) rs142354704
NM_032578.3(MYPN):c.3935G>A (p.Arg1312Gln) rs761812034
NM_032578.3(MYPN):c.410G>C (p.Arg137Thr) rs765931465
NM_032578.3(MYPN):c.411G>C (p.Arg137Ser) rs751085897
NM_032578.3(MYPN):c.625_627TCT[1] (p.Ser210del) rs749944961
NM_032578.3(MYPN):c.641C>T (p.Pro214Leu) rs1406498336
NM_032578.3(MYPN):c.65C>G (p.Ala22Gly) rs145142157
NM_032578.3(MYPN):c.712G>A (p.Ala238Thr) rs755212697
NM_032578.3(MYPN):c.729T>G (p.Ser243Arg) rs794727304
NM_032578.3(MYPN):c.734C>G (p.Ala245Gly) rs143574079
NM_032578.3(MYPN):c.757G>C (p.Gly253Arg) rs201983087
NM_032578.3(MYPN):c.845A>G (p.Glu282Gly) rs146336815
NM_032578.3(MYPN):c.903-4G>T rs886039040

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