ClinVar Miner

List of variants in gene MYPN reported as benign for Cardiovascular phenotype

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_032578.4(MYPN):c.1647T>C (p.Ser549=) rs2673794 0.57747
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.1875C>T (p.Pro625=) rs2673793 0.17340
NM_032578.4(MYPN):c.1869C>A (p.Thr623=) rs61854624 0.12645
NM_032578.4(MYPN):c.1178T>C (p.Val393Ala) rs11596653 0.11086
NM_032578.4(MYPN):c.1251G>A (p.Gln417=) rs10997948 0.10147
NM_032578.4(MYPN):c.1399G>A (p.Glu467Lys) rs74143030 0.04308
NM_032578.4(MYPN):c.2163C>A (p.Ala721=) rs71584491 0.04239
NM_032578.4(MYPN):c.843A>G (p.Pro281=) rs74143022 0.03534
NM_032578.4(MYPN):c.2410G>A (p.Gly804Arg) rs62620248 0.01839
NM_032578.4(MYPN):c.3279C>T (p.Asp1093=) rs115033934 0.01152
NM_032578.4(MYPN):c.2447C>T (p.Pro816Leu) rs111965755 0.01059
NM_032578.4(MYPN):c.1134C>T (p.Ile378=) rs145701607 0.00504
NM_032578.4(MYPN):c.3078G>A (p.Gly1026=) rs114479328 0.00385
NM_032578.4(MYPN):c.3421G>A (p.Ala1141Thr) rs150404143 0.00321
NM_032578.4(MYPN):c.3335C>T (p.Pro1112Leu) rs71534278 0.00318
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730 0.00123
NM_032578.2:c.2886T>C
NM_032578.4(MYPN):c.2409C>G (p.Ser803Arg) rs3814182

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