ClinVar for Gene (Select 83660) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3025496	NM_015059.3(TLN2):c.5133C>T (p.Ile1711=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2685519	GRCh37/hg19 15q22.2(chr15:63005171-63185575)x1	TLN2	Copy number loss	not provided	GUncertain significance
Select item 2645423	NM_015059.3(TLN2):c.7333G>T (p.Val2445Leu)	TLN2 (V2445L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2645422	NM_015059.3(TLN2):c.7257C>T (p.His2419=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645421	NM_015059.3(TLN2):c.7158C>T (p.Asp2386=)	LOC126862153, TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645420	NM_015059.3(TLN2):c.6716G>A (p.Arg2239His)	TLN2 (R2239H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2645419	NM_015059.3(TLN2):c.6654G>A (p.Thr2218=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645418	NM_015059.3(TLN2):c.6505A>G (p.Lys2169Glu)	TLN2 (K2169E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2645417	NM_015059.3(TLN2):c.5876C>T (p.Thr1959Met)	TLN2 (T1959M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2645416	NM_015059.3(TLN2):c.5598G>A (p.Ala1866=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645415	NM_015059.3(TLN2):c.5073G>A (p.Thr1691=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645414	NM_015059.3(TLN2):c.4932C>T (p.Asp1644=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645413	NM_015059.3(TLN2):c.4620C>T (p.Asn1540=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645412	NM_015059.3(TLN2):c.4095C>T (p.Cys1365=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645411	NM_015059.3(TLN2):c.3120G>A (p.Ser1040=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645410	NM_015059.3(TLN2):c.2937T>C (p.Ala979=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645409	NM_015059.3(TLN2):c.2865C>T (p.Val955=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645408	NM_015059.3(TLN2):c.1476C>T (p.Thr492=)	LOC121530585, TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645407	NM_015059.3(TLN2):c.1374G>A (p.Ser458=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2645406	NM_015059.3(TLN2):c.912C>T (p.Leu304=)	TLN2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2623254	NM_015059.3(TLN2):c.4732G>A (p.Ala1578Thr)	TLN2 (A1578T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2619270	NM_015059.3(TLN2):c.6529A>G (p.Ile2177Val)	TLN2 (I2177V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2613713	NM_015059.3(TLN2):c.31C>T (p.Arg11Cys)	TLN2 (R11C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2611974	NM_015059.3(TLN2):c.6601G>A (p.Asp2201Asn)	TLN2 (D2201N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2609838	NM_015059.3(TLN2):c.7538G>A (p.Arg2513Gln)	TLN2 (R2513Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2609781	NM_015059.3(TLN2):c.1277C>G (p.Ser426Cys)	TLN2 (S426C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2606905	NM_015059.3(TLN2):c.3131A>G (p.His1044Arg)	TLN2 (H1044R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2601264	NM_015059.3(TLN2):c.6496G>A (p.Val2166Ile)	TLN2 (V2166I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2597751	NM_015059.3(TLN2):c.7625G>A (p.Gly2542Asp)	TLN2 (G2542D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2595683	NM_015059.3(TLN2):c.3529G>A (p.Ala1177Thr)	TLN2 (A1177T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2589595	NM_015059.3(TLN2):c.6125C>T (p.Pro2042Leu)	TLN2 (P2042L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2558640	NM_015059.3(TLN2):c.5013C>G (p.Asn1671Lys)	TLN2 (N1671K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2558403	NM_015059.3(TLN2):c.6653C>T (p.Thr2218Met)	TLN2 (T2218M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2555637	NM_015059.3(TLN2):c.1997G>C (p.Arg666Pro)	TLN2 (R666P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2551044	NM_015059.3(TLN2):c.2558T>C (p.Met853Thr)	TLN2 (M853T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548569	NM_015059.3(TLN2):c.2546C>T (p.Ala849Val)	TLN2 (A849V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548220	NM_015059.3(TLN2):c.1649T>C (p.Val550Ala)	TLN2 (V550A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545975	NM_015059.3(TLN2):c.2664C>A (p.Asp888Glu)	TLN2 (D888E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2542387	NM_015059.3(TLN2):c.910C>T (p.Leu304Phe)	TLN2 (L304F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2530249	NM_015059.3(TLN2):c.1872C>A (p.Asp624Glu)	TLN2 (D624E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2530225	NM_015059.3(TLN2):c.2404G>A (p.Asp802Asn)	TLN2 (D802N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2524559	NM_015059.3(TLN2):c.2167G>A (p.Ala723Thr)	TLN2 (A723T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522403	NM_015059.3(TLN2):c.4664A>C (p.Asp1555Ala)	TLN2 (D1555A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515997	NM_015059.3(TLN2):c.904G>A (p.Val302Ile)	TLN2 (V302I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514692	NM_015059.3(TLN2):c.368T>C (p.Ile123Thr)	TLN2 (I123T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2509035	NM_015059.3(TLN2):c.1820G>A (p.Ser607Asn)	TLN2 (S607N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2508529	NM_015059.3(TLN2):c.277C>T (p.Arg93Trp)	TLN2 (R93W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2507569	NM_015059.3(TLN2):c.2596T>G (p.Leu866Val)	TLN2 (L866V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492915	NM_015059.3(TLN2):c.5606C>T (p.Ala1869Val)	TLN2 (A1869V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492914	NM_015059.3(TLN2):c.2812T>A (p.Ser938Thr)	TLN2 (S938T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2492203	NM_015059.3(TLN2):c.5462A>C (p.Glu1821Ala)	TLN2 (E1821A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491998	NM_015059.3(TLN2):c.5143A>G (p.Ile1715Val)	TLN2 (I1715V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488552	NM_015059.3(TLN2):c.1723G>C (p.Ala575Pro)	TLN2 (A575P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2487624	NM_015059.3(TLN2):c.7158C>A (p.Asp2386Glu)	LOC126862153, TLN2 (D2386E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2476400	NM_015059.3(TLN2):c.3459G>A (p.Met1153Ile)	TLN2 (M1153I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460790	NM_015059.3(TLN2):c.4855G>A (p.Ala1619Thr)	TLN2 (A1619T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2459531	NM_015059.3(TLN2):c.2314G>A (p.Ala772Thr)	TLN2 (A772T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2458749	NM_015059.3(TLN2):c.1562C>T (p.Ser521Leu)	LOC121530585, TLN2 (S521L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2456428	NM_015059.3(TLN2):c.1918G>A (p.Val640Ile)	TLN2 (V640I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2424797	NC_000015.9:g.(?_62146656)_(64747263_?)del	FBXL22, TLN2 +20 more	Deletion	not provided	GPathogenic
Select item 2411371	NM_015059.3(TLN2):c.3254C>T (p.Thr1085Met)	TLN2 (T1085M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2410117	NM_015059.3(TLN2):c.5900C>T (p.Ser1967Leu)	TLN2 (S1967L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2407040	NM_015059.3(TLN2):c.1813G>T (p.Val605Leu)	TLN2 (V605L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2406207	NM_015059.3(TLN2):c.7300G>A (p.Ala2434Thr)	TLN2 (A2434T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2400722	NM_015059.3(TLN2):c.2437G>A (p.Glu813Lys)	TLN2 (E813K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399816	NM_015059.3(TLN2):c.1924A>G (p.Thr642Ala)	TLN2 (T642A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399531	NM_015059.3(TLN2):c.2236G>A (p.Val746Met)	TLN2 (V746M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2397420	NM_015059.3(TLN2):c.6106T>G (p.Ser2036Ala)	TLN2 (S2036A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2394177	NM_015059.3(TLN2):c.6322G>A (p.Asp2108Asn)	TLN2 (D2108N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2386459	NM_015059.3(TLN2):c.4489G>A (p.Ala1497Thr)	TLN2 (A1497T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2377804	NM_015059.3(TLN2):c.2255A>G (p.Asn752Ser)	TLN2 (N752S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2371147	NM_015059.3(TLN2):c.3172A>G (p.Thr1058Ala)	TLN2 (T1058A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2370022	NM_015059.3(TLN2):c.5197G>A (p.Val1733Met)	TLN2 (V1733M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2363690	NM_015059.3(TLN2):c.5050G>A (p.Ala1684Thr)	TLN2 (A1684T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361423	NM_015059.3(TLN2):c.7418G>A (p.Arg2473His)	TLN2 (R2473H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2358427	NM_015059.3(TLN2):c.2326G>A (p.Val776Met)	TLN2 (V776M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355342	NM_015059.3(TLN2):c.1204A>G (p.Ile402Val)	TLN2 (I402V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351252	NM_015059.3(TLN2):c.865T>C (p.Cys289Arg)	TLN2 (C289R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347988	NM_015059.3(TLN2):c.4058C>G (p.Thr1353Ser)	TLN2 (T1353S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2339912	NM_015059.3(TLN2):c.620A>T (p.Asp207Val)	TLN2 (D207V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2339698	NM_015059.3(TLN2):c.6352G>T (p.Ala2118Ser)	TLN2 (A2118S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2331693	NM_015059.3(TLN2):c.6637G>A (p.Val2213Met)	TLN2 (V2213M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2326664	NM_015059.3(TLN2):c.5561A>G (p.Tyr1854Cys)	TLN2 (Y1854C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315905	NM_015059.3(TLN2):c.3224A>C (p.Glu1075Ala)	TLN2 (E1075A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314997	NM_015059.3(TLN2):c.3364G>A (p.Ala1122Thr)	TLN2 (A1122T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314692	NM_015059.3(TLN2):c.1293G>C (p.Lys431Asn)	TLN2 (K431N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2312110	NM_015059.3(TLN2):c.6857A>G (p.Gln2286Arg)	TLN2 (Q2286R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2305722	NM_015059.3(TLN2):c.6571G>A (p.Val2191Met)	TLN2 (V2191M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2299915	NM_015059.3(TLN2):c.3211A>G (p.Met1071Val)	TLN2 (M1071V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2297751	NM_015059.3(TLN2):c.1322G>A (p.Arg441Gln)	TLN2 (R441Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2297237	NM_015059.3(TLN2):c.3553C>G (p.Gln1185Glu)	TLN2 (Q1185E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2288701	NM_015059.3(TLN2):c.2747T>C (p.Ile916Thr)	TLN2 (I916T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2286956	NM_015059.3(TLN2):c.6772A>G (p.Ile2258Val)	TLN2 (I2258V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2285349	NM_015059.3(TLN2):c.5263C>G (p.Leu1755Val)	TLN2 (L1755V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2283084	NM_015059.3(TLN2):c.4822A>G (p.Met1608Val)	TLN2 (M1608V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278335	NM_015059.3(TLN2):c.5932G>A (p.Ala1978Thr)	TLN2 (A1978T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2277762	NM_015059.3(TLN2):c.2669A>G (p.Gln890Arg)	TLN2 (Q890R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2277412	NM_015059.3(TLN2):c.1082G>T (p.Arg361Leu)	TLN2 (R361L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2277179	NM_015059.3(TLN2):c.420A>C (p.Lys140Asn)	TLN2 (K140N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2271163	NM_015059.3(TLN2):c.2813C>G (p.Ser938Cys)	TLN2 (S938C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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