ClinVar Miner

List of variants in gene MKNK2

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_199054.3(MKNK2):c.25C>A (p.Leu9Ile) rs562548979 0.00018
NM_199054.3(MKNK2):c.1334C>T (p.Ala445Val) rs145777830 0.00017
NM_199054.3(MKNK2):c.1145T>C (p.Val382Ala) rs769652324 0.00009
NM_199054.3(MKNK2):c.48C>G (p.Phe16Leu) rs768284420 0.00009
NM_199054.3(MKNK2):c.523C>T (p.Arg175Trp) rs199860780 0.00007
NM_199054.3(MKNK2):c.148G>A (p.Ala50Thr) rs139681671 0.00006
NM_199054.3(MKNK2):c.202C>T (p.Arg68Cys) rs368662662 0.00003
NM_199054.3(MKNK2):c.74C>T (p.Ala25Val) rs1254577594 0.00001
NM_199054.3(MKNK2):c.76T>G (p.Phe26Val) rs1180915717 0.00001
NM_199054.3(MKNK2):c.77T>C (p.Phe26Ser) rs1483411819 0.00001
NM_199054.3(MKNK2):c.1006C>T (p.His336Tyr)
NM_199054.3(MKNK2):c.100G>A (p.Gly34Arg)
NM_199054.3(MKNK2):c.1087C>G (p.Leu363Val)
NM_199054.3(MKNK2):c.1114G>A (p.Ala372Thr)
NM_199054.3(MKNK2):c.1115C>T (p.Ala372Val)
NM_199054.3(MKNK2):c.1132C>G (p.Pro378Ala) rs2016844943
NM_199054.3(MKNK2):c.1158C>T (p.Asn386=)
NM_199054.3(MKNK2):c.1256C>A (p.Ala419Glu)
NM_199054.3(MKNK2):c.1256C>T (p.Ala419Val) rs374115536
NM_199054.3(MKNK2):c.1273G>A (p.Val425Ile)
NM_199054.3(MKNK2):c.130G>A (p.Ala44Thr) rs762788078
NM_199054.3(MKNK2):c.1339C>T (p.Arg447Trp)
NM_199054.3(MKNK2):c.133C>T (p.Arg45Cys)
NM_199054.3(MKNK2):c.1388A>T (p.Asp463Val) rs2016829842
NM_199054.3(MKNK2):c.1393G>A (p.Ala465Thr)
NM_199054.3(MKNK2):c.170C>T (p.Pro57Leu)
NM_199054.3(MKNK2):c.215C>T (p.Thr72Ile) rs2512026835
NM_199054.3(MKNK2):c.26T>C (p.Leu9Pro) rs2512033174
NM_199054.3(MKNK2):c.302G>A (p.Cys101Tyr)
NM_199054.3(MKNK2):c.367C>T (p.Arg123Trp)
NM_199054.3(MKNK2):c.379T>C (p.Phe127Leu) rs2512023389
NM_199054.3(MKNK2):c.385G>A (p.Glu129Lys) rs2512023379
NM_199054.3(MKNK2):c.503T>C (p.Leu168Pro) rs2512021758
NM_199054.3(MKNK2):c.514C>G (p.His172Asp) rs763807583
NM_199054.3(MKNK2):c.66C>G (p.Phe22Leu) rs202212307
NM_199054.3(MKNK2):c.706A>C (p.Asn236His) rs2512020958
NM_199054.3(MKNK2):c.77T>G (p.Phe26Cys)

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