ClinVar Miner

List of variants in gene MYPN reported as benign by Ambry Genetics

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Gene type:
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Total variants: 22
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NM_032578.4(MYPN):c.1134C>T (p.Ile378=) rs145701607
NM_032578.4(MYPN):c.1178T>C (p.Val393Ala) rs11596653
NM_032578.4(MYPN):c.1251G>A (p.Gln417=) rs10997948
NM_032578.4(MYPN):c.1399G>A (p.Glu467Lys) rs74143030
NM_032578.4(MYPN):c.1647T>C (p.Ser549=) rs2673794
NM_032578.4(MYPN):c.1869C>A (p.Thr623=) rs61854624
NM_032578.4(MYPN):c.1875C>T (p.Pro625=) rs2673793
NM_032578.4(MYPN):c.1884C>G (p.Phe628Leu) rs10823148
NM_032578.4(MYPN):c.2072G>A (p.Ser691Asn) rs10997975
NM_032578.4(MYPN):c.2120G>A (p.Ser707Asn) rs7916821
NM_032578.4(MYPN):c.2163C>A (p.Ala721=) rs71584491
NM_032578.4(MYPN):c.2409C>G (p.Ser803Arg) rs3814182
NM_032578.4(MYPN):c.2410G>A (p.Gly804Arg) rs62620248
NM_032578.4(MYPN):c.2447C>T (p.Pro816Leu) rs111965755
NM_032578.4(MYPN):c.3078G>A (p.Gly1026=) rs114479328
NM_032578.4(MYPN):c.3279C>T (p.Asp1093=) rs115033934
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278
NM_032578.4(MYPN):c.3403C>A (p.Pro1135Thr) rs7079481
NM_032578.4(MYPN):c.3421G>A (p.Ala1141Thr) rs150404143
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730
NM_032578.4(MYPN):c.843A>G (p.Pro281=) rs74143022

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