ClinVar Miner

List of variants in gene DMP1 reported as likely benign for not provided

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_004407.4(DMP1):c.1388A>G (p.Lys463Arg) rs34661425 0.01341
NM_004407.4(DMP1):c.103-318A>G rs146295699 0.00905
NM_004407.4(DMP1):c.815G>A (p.Arg272His) rs145237146 0.00202
NM_004407.4(DMP1):c.263C>T (p.Ala88Val) rs144773084 0.00092
NM_004407.4(DMP1):c.724T>C (p.Ser242Pro) rs147552663 0.00080
NM_004407.4(DMP1):c.312C>T (p.Asp104=) rs148543792 0.00070
NM_004407.4(DMP1):c.943G>C (p.Gly315Arg) rs149603030 0.00069
NM_004407.4(DMP1):c.997G>A (p.Val333Ile) rs147275271 0.00055
NM_004407.4(DMP1):c.1107C>T (p.Asp369=) rs147451774 0.00049
NM_004407.4(DMP1):c.1356C>T (p.Asp452=) rs149026481 0.00043
NM_004407.4(DMP1):c.79T>C (p.Ser27Pro) rs150105108 0.00018
NM_004407.4(DMP1):c.1396A>G (p.Ser466Gly) rs770626072 0.00017
NM_004407.4(DMP1):c.1062G>A (p.Glu354=) rs200640698 0.00011
NM_004407.4(DMP1):c.348C>T (p.Asp116=) rs147265141 0.00011
NM_004407.4(DMP1):c.1332C>T (p.Ser444=) rs375513808 0.00004
NM_004407.4(DMP1):c.135+15T>C rs1048327009 0.00001
NM_004407.4(DMP1):c.246A>G (p.Gln82=) rs1422654841 0.00001
NM_004407.4(DMP1):c.402G>A (p.Leu134=) rs780110476 0.00001
NM_004407.4(DMP1):c.753T>C (p.Thr251=) rs756758638 0.00001
NM_004407.4(DMP1):c.102+13A>G
NM_004407.4(DMP1):c.103-11C>T
NM_004407.4(DMP1):c.103-17_103-14del
NM_004407.4(DMP1):c.1080G>A (p.Val360=)
NM_004407.4(DMP1):c.1167G>A (p.Ser389=)
NM_004407.4(DMP1):c.1185A>C (p.Ser395=) rs142714056
NM_004407.4(DMP1):c.1206G>A (p.Glu402=)
NM_004407.4(DMP1):c.1257G>A (p.Pro419=)
NM_004407.4(DMP1):c.1287C>T (p.Ser429=)
NM_004407.4(DMP1):c.1299C>G (p.Leu433=)
NM_004407.4(DMP1):c.1347T>C (p.Ser449=)
NM_004407.4(DMP1):c.1353A>G (p.Glu451=)
NM_004407.4(DMP1):c.136-19A>C
NM_004407.4(DMP1):c.138G>A (p.Glu46=) rs1728793604
NM_004407.4(DMP1):c.1395T>C (p.Asp465=)
NM_004407.4(DMP1):c.1407G>A (p.Thr469=)
NM_004407.4(DMP1):c.1434T>C (p.Asp478=)
NM_004407.4(DMP1):c.1479T>C (p.Val493=)
NM_004407.4(DMP1):c.1488T>C (p.Tyr496=)
NM_004407.4(DMP1):c.1527C>T (p.Cys509=)
NM_004407.4(DMP1):c.1533C>T (p.Asp511=)
NM_004407.4(DMP1):c.184-12C>T
NM_004407.4(DMP1):c.184-13C>T
NM_004407.4(DMP1):c.184-4C>A
NM_004407.4(DMP1):c.195C>T (p.Asp65=)
NM_004407.4(DMP1):c.293GAG[1] (p.Gly99del) rs576066727
NM_004407.4(DMP1):c.318A>G (p.Glu106=)
NM_004407.4(DMP1):c.351T>C (p.Asp117=)
NM_004407.4(DMP1):c.360C>T (p.Gly120=)
NM_004407.4(DMP1):c.421G>A (p.Asp141Asn)
NM_004407.4(DMP1):c.480T>C (p.Asp160=)
NM_004407.4(DMP1):c.522G>A (p.Val174=)
NM_004407.4(DMP1):c.54+18G>A
NM_004407.4(DMP1):c.55-13C>T
NM_004407.4(DMP1):c.603G>A (p.Glu201=)
NM_004407.4(DMP1):c.609C>T (p.Ser203=)
NM_004407.4(DMP1):c.618C>T (p.Asp206=)
NM_004407.4(DMP1):c.624C>T (p.Ser208=)
NM_004407.4(DMP1):c.660A>C (p.Pro220=) rs2110016749
NM_004407.4(DMP1):c.708C>A (p.Gly236=)
NM_004407.4(DMP1):c.750C>T (p.Asn250=)
NM_004407.4(DMP1):c.810G>A (p.Lys270=) rs1415982839
NM_004407.4(DMP1):c.822A>G (p.Ser274=)
NM_004407.4(DMP1):c.825G>A (p.Glu275=)
NM_004407.4(DMP1):c.844C>A (p.Leu282Ile) rs141979823
NM_004407.4(DMP1):c.918C>T (p.Leu306=)
NM_004407.4(DMP1):c.996C>T (p.Asn332=)

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