TNKS[gene] and "single gene"[properties] - ClinVar

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Items: 82

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2488138	NM_003747.3(TNKS):c.8C>A (p.Ala3Glu)	TNKS (A3E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180436	NM_003747.3(TNKS):c.27T>A (p.His9Gln)	TNKS (H9Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515735	NM_003747.3(TNKS):c.31C>T (p.His11Tyr)	TNKS (H11Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208435	NM_003747.3(TNKS):c.58C>G (p.Pro20Ala)	TNKS (P20A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327596	NM_003747.3(TNKS):c.59C>T (p.Pro20Leu)	TNKS (P20L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180445	NM_003747.3(TNKS):c.67G>C (p.Gly23Arg)	TNKS (G23R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2690244	NM_003747.3(TNKS):c.71C>T (p.Ala24Val)	TNKS (A24V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2514138	NM_003747.3(TNKS):c.103C>G (p.Leu35Val)	TNKS (L35V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335785	NM_003747.3(TNKS):c.122C>T (p.Pro41Leu)	TNKS (P41L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388944	NM_003747.3(TNKS):c.124G>C (p.Gly42Arg)	TNKS (G42R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280408	NM_003747.3(TNKS):c.166T>G (p.Phe56Val)	TNKS (F56V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180431	NM_003747.3(TNKS):c.173C>G (p.Ser58Cys)	TNKS (S58C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263214	NM_003747.3(TNKS):c.206A>G (p.Asp69Gly)	TNKS (D69G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244410	NM_003747.3(TNKS):c.230G>A (p.Arg77Lys)	TNKS (R77K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373339	NM_003747.3(TNKS):c.239C>T (p.Ser80Phe)	TNKS (S80F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532447	NM_003747.3(TNKS):c.271A>G (p.Ser91Gly)	TNKS (S91G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550020	NM_003747.3(TNKS):c.274A>G (p.Thr92Ala)	TNKS (T92A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789760	NM_003747.3(TNKS):c.285A>T (p.Thr95=)	TNKS	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3180438	NM_003747.3(TNKS):c.296T>G (p.Val99Gly)	TNKS (V99G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363333	NM_003747.3(TNKS):c.358C>G (p.Pro120Ala)	TNKS (P120A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334343	NM_003747.3(TNKS):c.424T>C (p.Ser142Pro)	TNKS (S142P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250784	NM_003747.3(TNKS):c.427C>G (p.Pro143Ala)	TNKS (P143A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787328	NM_003747.3(TNKS):c.444G>A (p.Ser148=)	TNKS	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3180444	NM_003747.3(TNKS):c.447C>G (p.Ser149Arg)	TNKS (S149R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614502	NM_003747.3(TNKS):c.458G>A (p.Ser153Asn)	TNKS (S153N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260050	NM_003747.3(TNKS):c.587C>G (p.Ser196Cys)	TNKS (S196C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 774240	NM_003747.3(TNKS):c.674-5T>C	TNKS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2274295	NM_003747.3(TNKS):c.711G>T (p.Gln237His)	TNKS (Q237H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396273	NM_003747.3(TNKS):c.733C>T (p.Arg245Cys)	TNKS (R245C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324763	NM_003747.3(TNKS):c.796A>C (p.Ser266Arg)	TNKS (S266R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308936	NM_003747.3(TNKS):c.853C>T (p.Pro285Ser)	TNKS (P285S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590586	NM_003747.3(TNKS):c.866C>G (p.Ala289Gly)	TNKS (A289G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180446	NM_003747.3(TNKS):c.913G>A (p.Gly305Arg)	TNKS (G305R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611671	NM_003747.3(TNKS):c.1037G>A (p.Gly346Asp)	TNKS (G346D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 769740	NM_003747.3(TNKS):c.1047A>G (p.Glu349=)	TNKS	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2316058	NM_003747.3(TNKS):c.1058C>A (p.Ala353Asp)	TNKS (A353D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180428	NM_003747.3(TNKS):c.1111A>T (p.Thr371Ser)	TNKS (T371S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180429	NM_003747.3(TNKS):c.1148G>A (p.Arg383Gln)	TNKS (R383Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327597	NM_003747.3(TNKS):c.1172A>T (p.His391Leu)	TNKS (H391L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 715723	NM_003747.3(TNKS):c.1456+4C>T	TNKS	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3180430	NM_003747.3(TNKS):c.1528G>A (p.Ala510Thr)	TNKS (A510T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327599	NM_003747.3(TNKS):c.1556C>T (p.Pro519Leu)	TNKS (P519L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328914	NM_003747.3(TNKS):c.1639A>G (p.Lys547Glu)	TNKS (K547E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616839	NM_003747.3(TNKS):c.1709A>G (p.His570Arg)	TNKS (H570R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180432	NM_003747.3(TNKS):c.1750A>T (p.Met584Leu)	TNKS (M584L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382054	NM_003747.3(TNKS):c.1895A>G (p.Asn632Ser)	TNKS (N632S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180434	NM_003747.3(TNKS):c.2089G>A (p.Val697Met)	TNKS (V697M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463623	NM_003747.3(TNKS):c.2132A>G (p.His711Arg)	TNKS (H711R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280450	NM_003747.3(TNKS):c.2302C>A (p.Leu768Ile)	TNKS (L768I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 713361	NM_003747.3(TNKS):c.2331T>C (p.Thr777=)	TNKS	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2233733	NM_003747.3(TNKS):c.2429C>T (p.Ala810Val)	TNKS (A810V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180435	NM_003747.3(TNKS):c.2474C>T (p.Pro825Leu)	TNKS (P825L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333210	NM_003747.3(TNKS):c.2547C>G (p.Asn849Lys)	TNKS (N849K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614704	NM_003747.3(TNKS):c.2558C>G (p.Ala853Gly)	TNKS (A853G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327598	NM_003747.3(TNKS):c.2747C>T (p.Thr916Met)	TNKS (T916M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180437	NM_003747.3(TNKS):c.2812A>G (p.Thr938Ala)	TNKS (T938A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268982	NM_003747.3(TNKS):c.2872C>T (p.Pro958Ser)	TNKS (P958S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327601	NM_003747.3(TNKS):c.2917A>G (p.Ser973Gly)	TNKS (S973G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377657	NM_003747.3(TNKS):c.2948C>G (p.Pro983Arg)	TNKS (P983R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304509	NM_003747.3(TNKS):c.2948C>T (p.Pro983Leu)	TNKS (P983L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 709259	NM_003747.3(TNKS):c.2949C>T (p.Pro983=)	TNKS	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2486149	NM_003747.3(TNKS):c.2998G>A (p.Ala1000Thr)	TNKS (A1000T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268186	NM_003747.3(TNKS):c.3059A>G (p.Lys1020Arg)	TNKS (K1020R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180439	NM_003747.3(TNKS):c.3107A>C (p.Lys1036Thr)	TNKS (K1036T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533178	NM_003747.3(TNKS):c.3263G>A (p.Gly1088Asp)	TNKS (G1088D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241902	NM_003747.3(TNKS):c.3293C>G (p.Thr1098Ser)	TNKS (T1098S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180440	NM_003747.3(TNKS):c.3301T>C (p.Cys1101Arg)	TNKS (C1101R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327595	NM_003747.3(TNKS):c.3317C>T (p.Thr1106Met)	TNKS (T1106M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543301	NM_003747.3(TNKS):c.3468G>C (p.Lys1156Asn)	TNKS (K1156N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391487	NM_003747.3(TNKS):c.3470A>G (p.Lys1157Arg)	TNKS (K1157R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270537	NM_003747.3(TNKS):c.3488G>A (p.Cys1163Tyr)	TNKS (C1163Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180441	NM_003747.3(TNKS):c.3566T>C (p.Ile1189Thr)	TNKS (I1189T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180442	NM_003747.3(TNKS):c.3638A>G (p.Tyr1213Cys)	TNKS (Y1213C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3180443	NM_003747.3(TNKS):c.3764C>T (p.Thr1255Ile)	TNKS (T1255I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273027	NM_003747.3(TNKS):c.3797T>C (p.Met1266Thr)	TNKS (M1266T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3327600	NM_003747.3(TNKS):c.3836T>C (p.Ile1279Thr)	TNKS (I1279T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273790	NM_003747.3(TNKS):c.3958G>A (p.Ala1320Thr)	TNKS (A1320T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1340690	GRCh37/hg19 8p23.1(chr8:9447087-9687874)x3	TNKS	Copy number gain	not provided	GUncertain significance
Select item 980853	GRCh37/hg19 8p23.1(chr8:9511554-9647023)x3	TNKS	Copy number gain	not provided	GUncertain significance
Select item 980852	GRCh37/hg19 8p23.1(chr8:9010028-9567941)x3	TNKS	Copy number gain	not provided	GUncertain significance
Select item 815093	GRCh37/hg19 8p23.1(chr8:9613875-9742841)x3	TNKS	Copy number gain	not provided	GUncertain significance
Select item 815091	GRCh37/hg19 8p23.1(chr8:9171734-9608096)x1	TNKS	Copy number loss	not provided	GUncertain significance

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Items: 82