ClinVar Miner

List of variants in gene MYPN reported as uncertain significance by Biesecker Lab/Clinical Genomics Section,National Institutes of Health

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Gene type:
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Total variants: 16
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HGVS dbSNP
NM_032578.3(MYPN):c.1130G>A (p.Arg377Gln) rs147596628
NM_032578.3(MYPN):c.1238T>C (p.Ile413Thr) rs201225230
NM_032578.3(MYPN):c.1858A>G (p.Thr620Ala) rs144031245
NM_032578.3(MYPN):c.185A>C (p.Asp62Ala) rs370768715
NM_032578.3(MYPN):c.2042C>T (p.Pro681Leu) rs202084832
NM_032578.3(MYPN):c.2260A>C (p.Ile754Leu) rs201245117
NM_032578.3(MYPN):c.2560T>A (p.Ser854Thr) rs200432306
NM_032578.3(MYPN):c.2756G>A (p.Arg919His) rs193022869
NM_032578.3(MYPN):c.2864G>A (p.Arg955Gln) rs199476414
NM_032578.3(MYPN):c.2981T>C (p.Met994Thr) rs786205348
NM_032578.3(MYPN):c.3335C>A (p.Pro1112His) rs71534278
NM_032578.3(MYPN):c.3440T>A (p.Ile1147Asn) rs201600440
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.662A>T (p.Asp221Val) rs185841477

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