ClinVar for Gene (Select 158471) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3310791	NM_015225.3(PRUNE2):c.3276C>A (p.Asn1092Lys)	PRUNE2 (N1092K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310790	NM_015225.3(PRUNE2):c.3901G>A (p.Ala1301Thr)	PRUNE2 (A1301T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310789	NM_015225.3(PRUNE2):c.1798A>G (p.Arg600Gly)	PRUNE2 (R600G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310788	NM_015225.3(PRUNE2):c.818T>G (p.Phe273Cys)	PRUNE2 (F273C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310787	NM_015225.3(PRUNE2):c.403G>A (p.Asp135Asn)	PRUNE2 (D135N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310786	NM_015225.3(PRUNE2):c.1738A>G (p.Asn580Asp)	PRUNE2 (N580D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310785	NM_015225.3(PRUNE2):c.7280C>A (p.Ala2427Glu)	PRUNE2 (A2427E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310784	NM_015225.3(PRUNE2):c.7421G>A (p.Gly2474Asp)	PRUNE2 (G2474D)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3310783	NM_015225.3(PRUNE2):c.997T>C (p.Tyr333His)	PRUNE2 (Y333H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310782	NM_015225.3(PRUNE2):c.1925G>A (p.Gly642Asp)	PRUNE2 (G642D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310781	NM_015225.3(PRUNE2):c.1153A>C (p.Ile385Leu)	PRUNE2 (I385L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310779	NM_015225.3(PRUNE2):c.2626A>T (p.Ile876Phe)	PRUNE2 (I876F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310778	NM_015225.3(PRUNE2):c.4100C>T (p.Ser1367Phe)	PRUNE2 (S1367F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310777	NM_015225.3(PRUNE2):c.1261G>A (p.Val421Ile)	PRUNE2 (V421I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3310776	NM_015225.3(PRUNE2):c.3260T>A (p.Leu1087Gln)	PRUNE2 (L1087Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310775	NM_015225.3(PRUNE2):c.1462G>A (p.Gly488Ser)	PRUNE2 (G488S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3310774	NM_015225.3(PRUNE2):c.8896G>A (p.Ala2966Thr)	PRUNE2 (A231T +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310773	NM_015225.3(PRUNE2):c.5191G>C (p.Asp1731His)	PRUNE2 (D1731H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310772	NM_015225.3(PRUNE2):c.8791A>C (p.Ser2931Arg)	PRUNE2 (S195R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3310771	NM_015225.3(PRUNE2):c.1498C>T (p.Pro500Ser)	PRUNE2 (P500S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310770	NM_015225.3(PRUNE2):c.5909C>T (p.Pro1970Leu)	PRUNE2 (P1970L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310769	NM_015225.3(PRUNE2):c.7908G>C (p.Leu2636Phe)	PRUNE2 (L2636F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310768	NM_015225.3(PRUNE2):c.7855G>A (p.Asp2619Asn)	PRUNE2 (D2619N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310767	NM_015225.3(PRUNE2):c.6301G>C (p.Ala2101Pro)	PRUNE2 (A2101P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3310766	NM_015225.3(PRUNE2):c.5614G>A (p.Val1872Ile)	PRUNE2 (V1872I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3310765	NM_015225.3(PRUNE2):c.1600G>A (p.Ala534Thr)	PRUNE2 (A534T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3220059	NM_015225.3(PRUNE2):c.9220T>A (p.Ser3074Thr)	PRUNE2 (S339T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220058	NM_015225.3(PRUNE2):c.8962C>T (p.Arg2988Trp)	PRUNE2 (R2992W +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220057	NM_015225.3(PRUNE2):c.8810A>G (p.Tyr2937Cys)	PRUNE2 (Y201C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220056	NM_015225.3(PRUNE2):c.8807A>G (p.His2936Arg)	PRUNE2 (H201R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220054	NM_015225.3(PRUNE2):c.8320G>A (p.Gly2774Ser)	PRUNE2 (G2774S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220053	NM_015225.3(PRUNE2):c.8176C>G (p.Leu2726Val)	PRUNE2 (L2726V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220051	NM_015225.3(PRUNE2):c.8068G>A (p.Glu2690Lys)	PRUNE2 (E2690K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220050	NM_015225.3(PRUNE2):c.7948G>T (p.Asp2650Tyr)	PRUNE2 (D2650Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220049	NM_015225.3(PRUNE2):c.7940A>T (p.Asp2647Val)	PRUNE2 (D2647V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220047	NM_015225.3(PRUNE2):c.7447G>T (p.Val2483Phe)	PRUNE2 (V2483F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220046	NM_015225.3(PRUNE2):c.7310G>A (p.Arg2437Gln)	PRUNE2 (R2437Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3220045	NM_015225.3(PRUNE2):c.7151C>G (p.Ser2384Cys)	PRUNE2 (S2384C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220044	NM_015225.3(PRUNE2):c.6867C>A (p.Asp2289Glu)	PRUNE2 (D2289E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220043	NM_015225.3(PRUNE2):c.6784G>A (p.Gly2262Ser)	PRUNE2 (G2262S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220042	NM_015225.3(PRUNE2):c.6658C>T (p.Pro2220Ser)	PRUNE2 (P2220S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220040	NM_015225.3(PRUNE2):c.6529A>G (p.Ile2177Val)	PRUNE2 (I2177V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220039	NM_015225.3(PRUNE2):c.6422T>C (p.Ile2141Thr)	PRUNE2 (I2141T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220037	NM_015225.3(PRUNE2):c.6287A>G (p.Asp2096Gly)	PRUNE2 (D2096G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220036	NM_015225.3(PRUNE2):c.6171T>A (p.Phe2057Leu)	PRUNE2 (F2057L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220035	NM_015225.3(PRUNE2):c.6019G>A (p.Glu2007Lys)	PRUNE2 (E2007K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220034	NM_015225.3(PRUNE2):c.5956A>T (p.Asn1986Tyr)	PRUNE2 (N1986Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220033	NM_015225.3(PRUNE2):c.587A>G (p.Glu196Gly)	PRUNE2 (E196G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220032	NM_015225.3(PRUNE2):c.5759A>G (p.Asp1920Gly)	PRUNE2 (D1920G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220031	NM_015225.3(PRUNE2):c.5749C>G (p.Pro1917Ala)	PRUNE2 (P1917A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220030	NM_015225.3(PRUNE2):c.5708C>T (p.Ser1903Phe)	PRUNE2 (S1903F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220029	NM_015225.3(PRUNE2):c.5635G>T (p.Val1879Leu)	PRUNE2 (V1879L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220027	NM_015225.3(PRUNE2):c.5627T>C (p.Ile1876Thr)	PRUNE2 (I1876T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3220026	NM_015225.3(PRUNE2):c.5434G>A (p.Glu1812Lys)	PRUNE2 (E1812K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220024	NM_015225.3(PRUNE2):c.4999C>T (p.His1667Tyr)	PRUNE2 (H1667Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220023	NM_015225.3(PRUNE2):c.4964G>A (p.Ser1655Asn)	PRUNE2 (S1655N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220022	NM_015225.3(PRUNE2):c.469C>T (p.Pro157Ser)	PRUNE2 (P157S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220021	NM_015225.3(PRUNE2):c.4645G>A (p.Glu1549Lys)	PRUNE2 (E1549K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220020	NM_015225.3(PRUNE2):c.4630A>G (p.Ser1544Gly)	PRUNE2 (S1544G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220019	NM_015225.3(PRUNE2):c.4556A>G (p.Glu1519Gly)	PRUNE2 (E1519G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220018	NM_015225.3(PRUNE2):c.4525A>G (p.Ile1509Val)	PRUNE2 (I1509V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220017	NM_015225.3(PRUNE2):c.4502A>G (p.His1501Arg)	PRUNE2 (H1501R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220016	NM_015225.3(PRUNE2):c.412G>A (p.Val138Ile)	PRUNE2 (V138I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220015	NM_015225.3(PRUNE2):c.3839T>C (p.Ile1280Thr)	PRUNE2 (I1280T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3220014	NM_015225.3(PRUNE2):c.3611A>G (p.His1204Arg)	PRUNE2 (H1204R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220013	NM_015225.3(PRUNE2):c.3494C>T (p.Thr1165Ile)	PRUNE2 (T1165I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220011	NM_015225.3(PRUNE2):c.3469A>G (p.Met1157Val)	PRUNE2 (M1157V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220010	NM_015225.3(PRUNE2):c.3308A>G (p.Asn1103Ser)	PRUNE2 (N1103S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220008	NM_015225.3(PRUNE2):c.2873C>T (p.Ser958Leu)	PRUNE2 (S958L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220007	NM_015225.3(PRUNE2):c.2834A>G (p.Lys945Arg)	PRUNE2 (K945R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220006	NM_015225.3(PRUNE2):c.2426A>G (p.Asp809Gly)	PRUNE2 (D809G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220005	NM_015225.3(PRUNE2):c.2327C>T (p.Thr776Ile)	PRUNE2 (T776I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220004	NM_015225.3(PRUNE2):c.230A>G (p.Glu77Gly)	PRUNE2 (E77G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3220003	NM_015225.3(PRUNE2):c.2285T>G (p.Ile762Arg)	PRUNE2 (I762R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3220000	NM_015225.3(PRUNE2):c.1759C>A (p.Leu587Met)	PRUNE2 (L587M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219999	NM_015225.3(PRUNE2):c.1466A>G (p.Glu489Gly)	PRUNE2 (E489G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219997	NM_015225.3(PRUNE2):c.1177A>G (p.Ile393Val)	PRUNE2 (I393V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3219996	NM_015225.3(PRUNE2):c.1067G>A (p.Arg356Lys)	PRUNE2 (R356K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063071	GRCh37/hg19 9p24.3-q34.3(chr9:203861-141020389)x3	DMAC1, DMRT1 +769 more	Copy number gain	not specified	GPathogenic
Select item 2659267	NM_015225.3(PRUNE2):c.483C>T (p.Thr161=)	PRUNE2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2659266	NM_015225.3(PRUNE2):c.1041C>T (p.Leu347=)	PRUNE2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2659265	NM_015225.3(PRUNE2):c.1132C>G (p.Leu378Val)	PRUNE2 (L378V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2659264	NM_015225.3(PRUNE2):c.3210C>T (p.Asp1070=)	PRUNE2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2659263	NM_015225.3(PRUNE2):c.3337G>A (p.Asp1113Asn)	PRUNE2 (D1113N)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2659262	NM_015225.3(PRUNE2):c.4854T>A (p.Thr1618=)	PRUNE2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2659261	NM_015225.3(PRUNE2):c.5070C>T (p.Asp1690=)	PRUNE2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2659260	NM_015225.3(PRUNE2):c.7854C>T (p.Ser2618=)	PRUNE2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2619999	NM_015225.3(PRUNE2):c.3179C>T (p.Thr1060Ile)	PRUNE2 (T1060I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619787	NM_015225.3(PRUNE2):c.4673C>A (p.Ser1558Tyr)	PRUNE2 (S1558Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617127	NM_015225.3(PRUNE2):c.7126G>A (p.Gly2376Ser)	PRUNE2 (G2376S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607853	NM_015225.3(PRUNE2):c.4229T>C (p.Leu1410Pro)	PRUNE2 (L1410P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2607792	NM_015225.3(PRUNE2):c.8641C>G (p.Leu2881Val)	PRUNE2 (L146V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2602178	NM_015225.3(PRUNE2):c.6898G>A (p.Asp2300Asn)	PRUNE2 (D2300N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601885	NM_015225.3(PRUNE2):c.1954C>T (p.Arg652Trp)	PRUNE2 (R652W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596977	NM_015225.3(PRUNE2):c.6626G>C (p.Gly2209Ala)	PRUNE2 (G2209A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596075	NM_015225.3(PRUNE2):c.6455A>T (p.Glu2152Val)	PRUNE2 (E2152V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590375	NM_015225.3(PRUNE2):c.9083A>G (p.Asn3028Ser)	PRUNE2 (N293S +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2588941	NM_015225.3(PRUNE2):c.1891A>G (p.Thr631Ala)	PRUNE2 (T631A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2560131	NM_015225.3(PRUNE2):c.1379A>G (p.His460Arg)	PRUNE2 (H460R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558625	NM_015225.3(PRUNE2):c.7552A>G (p.Thr2518Ala)	PRUNE2 (T2518A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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