ClinVar for Gene (Select 5591) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3225950	NM_006904.7(PRKDC):c.998T>C (p.Met333Thr)	PRKDC (M333T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225949	NM_006904.7(PRKDC):c.997A>G (p.Met333Val)	PRKDC (M333V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225948	NM_006904.7(PRKDC):c.9888G>T (p.Gln3296His)	PRKDC (Q3296H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225947	NM_006904.7(PRKDC):c.9874G>A (p.Gly3292Ser)	PRKDC (G3292S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3225946	NM_006904.7(PRKDC):c.968T>C (p.Val323Ala)	PRKDC (V323A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225945	NM_006904.7(PRKDC):c.9674A>G (p.Glu3225Gly)	PRKDC (E3225G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225944	NM_006904.7(PRKDC):c.9650G>T (p.Arg3217Met)	PRKDC (R3217M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225943	NM_006904.7(PRKDC):c.9624G>C (p.Val3208=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225942	NM_006904.7(PRKDC):c.957T>C (p.Phe319=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225941	NM_006904.7(PRKDC):c.9488C>A (p.Thr3163Asn)	PRKDC (T3163N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225940	NM_006904.7(PRKDC):c.9440A>G (p.Lys3147Arg)	PRKDC (K3147R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225938	NM_006904.7(PRKDC):c.9251A>G (p.Gln3084Arg)	PRKDC (Q3084R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225937	NM_006904.7(PRKDC):c.922T>C (p.Leu308=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225936	NM_006904.7(PRKDC):c.9213G>A (p.Gly3071=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225935	NM_006904.7(PRKDC):c.9212G>T (p.Gly3071Val)	PRKDC (G3071V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225934	NM_006904.7(PRKDC):c.9142A>G (p.Lys3048Glu)	PRKDC (K3048E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225933	NM_006904.7(PRKDC):c.8908A>C (p.Lys2970Gln)	PRKDC (K2970Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225932	NM_006904.7(PRKDC):c.885A>G (p.Glu295=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225931	NM_006904.7(PRKDC):c.881T>C (p.Phe294Ser)	PRKDC (F294S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225930	NM_006904.7(PRKDC):c.8760C>T (p.Val2920=)	LOC121740717, PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225929	NM_006904.7(PRKDC):c.8742C>G (p.Ala2914=)	LOC121740717, PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225928	NM_006904.7(PRKDC):c.8649C>A (p.Ser2883Arg)	LOC121740717, PRKDC (S2883R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225926	NM_006904.7(PRKDC):c.8533A>G (p.Asn2845Asp)	PRKDC (N2845D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225925	NM_006904.7(PRKDC):c.8375C>A (p.Thr2792Asn)	PRKDC (T2792N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225923	NM_006904.7(PRKDC):c.8255A>G (p.Lys2752Arg)	PRKDC (K2752R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225922	NM_006904.7(PRKDC):c.8201G>T (p.Arg2734Met)	PRKDC (R2734M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225921	NM_006904.7(PRKDC):c.8201G>A (p.Arg2734Lys)	PRKDC (R2734K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3225920	NM_006904.7(PRKDC):c.812G>T (p.Gly271Val)	PRKDC (G271V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225919	NM_006904.7(PRKDC):c.8126G>A (p.Gly2709Glu)	PRKDC (G2709E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225918	NM_006904.7(PRKDC):c.8111G>A (p.Arg2704Lys)	PRKDC (R2704K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225917	NM_006904.7(PRKDC):c.7888C>T (p.Pro2630Ser)	PRKDC (P2630S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225915	NM_006904.7(PRKDC):c.7729T>C (p.Phe2577Leu)	PRKDC (F2577L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225914	NM_006904.7(PRKDC):c.7660T>G (p.Phe2554Val)	PRKDC (F2554V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225913	NM_006904.7(PRKDC):c.760A>C (p.Lys254Gln)	PRKDC (K254Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225912	NM_006904.7(PRKDC):c.7599A>T (p.Ser2533=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225911	NM_006904.7(PRKDC):c.7589G>A (p.Arg2530Lys)	PRKDC (R2530K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225910	NM_006904.7(PRKDC):c.7562T>A (p.Ile2521Asn)	PRKDC (I2521N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225909	NM_006904.7(PRKDC):c.7495T>G (p.Phe2499Val)	PRKDC (F2499V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225908	NM_006904.7(PRKDC):c.746T>C (p.Phe249Ser)	PRKDC (F249S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225907	NM_006904.7(PRKDC):c.7436G>T (p.Trp2479Leu)	PRKDC (W2479L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225906	NM_006904.7(PRKDC):c.738G>T (p.Arg246Ser)	PRKDC (R246S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225905	NM_006904.7(PRKDC):c.7361T>G (p.Leu2454Arg)	PRKDC (L2454R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225904	NM_006904.7(PRKDC):c.7353C>G (p.Leu2451=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225903	NM_006904.7(PRKDC):c.728A>G (p.Gln243Arg)	PRKDC (Q243R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225902	NM_006904.7(PRKDC):c.709T>C (p.Ser237Pro)	PRKDC (S237P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225901	NM_006904.7(PRKDC):c.705T>C (p.Thr235=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225900	NM_006904.7(PRKDC):c.6941A>G (p.Glu2314Gly)	PRKDC (E2314G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225899	NM_006904.7(PRKDC):c.6847A>G (p.Asn2283Asp)	PRKDC (N2283D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225898	NM_006904.7(PRKDC):c.6847A>C (p.Asn2283His)	PRKDC (N2283H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225897	NM_006904.7(PRKDC):c.6793C>A (p.Pro2265Thr)	PRKDC (P2265T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225896	NM_006904.7(PRKDC):c.6773A>T (p.Glu2258Val)	PRKDC (E2258V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225895	NM_006904.7(PRKDC):c.674A>G (p.Lys225Arg)	PRKDC (K225R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225894	NM_006904.7(PRKDC):c.6708A>C (p.Glu2236Asp)	PRKDC (E2236D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225893	NM_006904.7(PRKDC):c.6680A>G (p.Lys2227Arg)	PRKDC (K2227R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225892	NM_006904.7(PRKDC):c.6643T>G (p.Leu2215Val)	PRKDC (L2215V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225891	NM_006904.7(PRKDC):c.6619A>C (p.Lys2207Gln)	PRKDC (K2207Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225890	NM_006904.7(PRKDC):c.6611G>T (p.Gly2204Val)	PRKDC (G2204V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225889	NM_006904.7(PRKDC):c.6581T>C (p.Leu2194Pro)	PRKDC (L2194P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225888	NM_006904.7(PRKDC):c.6461A>G (p.Glu2154Gly)	PRKDC (E2154G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225887	NM_006904.7(PRKDC):c.639A>G (p.Arg213=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225886	NM_006904.7(PRKDC):c.636A>G (p.Val212=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225885	NM_006904.7(PRKDC):c.6243G>C (p.Leu2081=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225884	NM_006904.7(PRKDC):c.6167C>G (p.Ser2056Cys)	PRKDC (S2056C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225883	NM_006904.7(PRKDC):c.60C>A (p.Ser20=)	LOC129929030, PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225882	NM_006904.7(PRKDC):c.6080C>G (p.Ser2027Cys)	PRKDC (S2027C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225881	NM_006904.7(PRKDC):c.605G>A (p.Gly202Asp)	PRKDC (G202D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225880	NM_006904.7(PRKDC):c.59C>T (p.Ser20Phe)	LOC129929030, PRKDC (S20F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225879	NM_006904.7(PRKDC):c.5949C>A (p.Asp1983Glu)	PRKDC (D1983E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225878	NM_006904.7(PRKDC):c.5888A>G (p.Gln1963Arg)	PRKDC (Q1963R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225877	NM_006904.7(PRKDC):c.5776A>G (p.Asn1926Asp)	PRKDC (N1926D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225876	NM_006904.7(PRKDC):c.5700C>T (p.Phe1900=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225875	NM_006904.7(PRKDC):c.5696T>G (p.Val1899Gly)	PRKDC (V1899G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225874	NM_006904.7(PRKDC):c.5678A>G (p.Glu1893Gly)	PRKDC (E1893G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225873	NM_006904.7(PRKDC):c.5291A>G (p.Glu1764Gly)	PRKDC (E1764G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225871	NM_006904.7(PRKDC):c.5232A>G (p.Lys1744=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225870	NM_006904.7(PRKDC):c.5191C>T (p.Pro1731Ser)	PRKDC (P1731S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225869	NM_006904.7(PRKDC):c.5052G>A (p.Leu1684=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225868	NM_006904.7(PRKDC):c.503A>T (p.Asp168Val)	PRKDC (D168V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225867	NM_006904.7(PRKDC):c.5005C>T (p.Pro1669Ser)	PRKDC (P1669S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225866	NM_006904.7(PRKDC):c.4981T>C (p.Phe1661Leu)	PRKDC (F1661L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225865	NM_006904.7(PRKDC):c.4968T>G (p.Asp1656Glu)	PRKDC (D1656E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225864	NM_006904.7(PRKDC):c.492A>G (p.Lys164=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225863	NM_006904.7(PRKDC):c.4771A>C (p.Lys1591Gln)	PRKDC (K1591Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225862	NM_006904.7(PRKDC):c.4695A>G (p.Glu1565=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225861	NM_006904.7(PRKDC):c.4674T>C (p.Tyr1558=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225860	NM_006904.7(PRKDC):c.444A>G (p.Lys148=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225858	NM_006904.7(PRKDC):c.4352T>C (p.Val1451Ala)	PRKDC (V1451A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225857	NM_006904.7(PRKDC):c.4344G>T (p.Leu1448=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225856	NM_006904.7(PRKDC):c.4251C>T (p.Thr1417=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225855	NM_006904.7(PRKDC):c.420T>C (p.Ser140=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225854	NM_006904.7(PRKDC):c.410C>T (p.Thr137Ile)	PRKDC (T137I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225853	NM_006904.7(PRKDC):c.4001A>T (p.Lys1334Ile)	PRKDC (K1334I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225852	NM_006904.7(PRKDC):c.3984A>C (p.Glu1328Asp)	PRKDC (E1328D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225851	NM_006904.7(PRKDC):c.388C>T (p.Leu130Phe)	PRKDC (L130F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225850	NM_006904.7(PRKDC):c.3783G>C (p.Leu1261=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225849	NM_006904.7(PRKDC):c.3753G>T (p.Gln1251His)	PRKDC (Q1251H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225848	NM_006904.7(PRKDC):c.3737G>T (p.Gly1246Val)	PRKDC (G1246V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225847	NM_006904.7(PRKDC):c.3717C>T (p.Pro1239=)	PRKDC	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225846	NM_006904.7(PRKDC):c.3695C>A (p.Pro1232His)	PRKDC (P1232H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225845	NM_006904.7(PRKDC):c.3689G>A (p.Gly1230Asp)	PRKDC (G1230D)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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