ClinVar Miner

List of variants in gene MYPN reported as likely benign for not provided

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Total variants: 23
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HGVS dbSNP
NM_032578.3(MYPN):c.1046C>A (p.Thr349Lys) rs763819518
NM_032578.3(MYPN):c.1078+69A>T
NM_032578.3(MYPN):c.1130+166A>G
NM_032578.3(MYPN):c.1131-170A>G
NM_032578.3(MYPN):c.1131-308C>A
NM_032578.3(MYPN):c.1601-50A>G
NM_032578.3(MYPN):c.1790G>A (p.Arg597His) rs150911078
NM_032578.3(MYPN):c.1840G>A (p.Glu614Lys) rs143338091
NM_032578.3(MYPN):c.1944G>A (p.Glu648=) rs151017803
NM_032578.3(MYPN):c.2703+172C>A
NM_032578.3(MYPN):c.2863C>T (p.Arg955Trp) rs149887823
NM_032578.3(MYPN):c.2925+121A>G
NM_032578.3(MYPN):c.3286-271T>G
NM_032578.3(MYPN):c.3441C>A (p.Ile1147=)
NM_032578.3(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730
NM_032578.3(MYPN):c.3660-208G>C
NM_032578.3(MYPN):c.3792C>T (p.Tyr1264=) rs142307556
NM_032578.3(MYPN):c.3846T>A (p.Ser1282Arg) rs147659164
NM_032578.3(MYPN):c.3963A>G (p.Ter1321=)
NM_032578.3(MYPN):c.410G>C (p.Arg137Thr) rs765931465
NM_032578.3(MYPN):c.59A>G (p.Tyr20Cys) rs140148105
NM_032578.3(MYPN):c.903-6045C>T
NM_032578.3(MYPN):c.952G>A (p.Val318Ile) rs112518450

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