ClinVar for Gene (Select 2322) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3279262	NM_004119.3(FLT3):c.2540A>G (p.Asn847Ser)	FLT3 (N847S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279261	NM_004119.3(FLT3):c.446C>A (p.Ala149Asp)	FLT3 (A149D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279260	NM_004119.3(FLT3):c.418G>C (p.Glu140Gln)	FLT3 (E140Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279259	NM_004119.3(FLT3):c.2417C>T (p.Ser806Leu)	FLT3 (S806L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3279258	NM_004119.3(FLT3):c.983A>C (p.Tyr328Ser)	FLT3 (Y328S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3244219	NC_000013.10:g.(?_27827914)_(29252239_?)dup	CDX2, FLT1 +13 more	Duplication	not provided	GUncertain significance
Select item 3148850	GRCh37/hg19 13q11-13.3(chr13:19436287-36278224)x3	CDX2, AMER2 +82 more	Copy number gain	not provided	GUncertain significance
Select item 3095737	NM_004119.3(FLT3):c.620A>T (p.Lys207Ile)	FLT3 (K207I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095736	NM_004119.3(FLT3):c.466T>C (p.Phe156Leu)	FLT3 (F156L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095735	NM_004119.3(FLT3):c.268A>G (p.Thr90Ala)	FLT3 (T90A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095734	NM_004119.3(FLT3):c.2336A>T (p.Asp779Val)	FLT3 (D779V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095733	NM_004119.3(FLT3):c.2021T>C (p.Ile674Thr)	FLT3 (I674T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095732	NM_004119.3(FLT3):c.185A>G (p.Asp62Gly)	FLT3 (D62G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095731	NM_004119.3(FLT3):c.1192G>T (p.Asp398Tyr)	FLT3 (D398Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095730	NM_004119.3(FLT3):c.1087C>G (p.Gln363Glu)	FLT3 (Q363E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3095729	NM_004119.3(FLT3):c.1001A>C (p.Lys334Thr)	FLT3 (K334T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063305	GRCh37/hg19 13q12.12-12.2(chr13:23329180-28663294)x3	AMER2, ATP12A +33 more	Copy number gain	not specified	GUncertain significance
Select item 3053518	NM_004119.3(FLT3):c.2439C>T (p.Ala813=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	FLT3-related disorder	GLikely benign
Select item 3047889	NM_004119.3(FLT3):c.285C>T (p.Val95=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	FLT3-related disorder	GLikely benign
Select item 3047481	NM_004119.3(FLT3):c.1337C>T (p.Ser446Leu)	FLT3 (S446L)	Single nucleotide variant (missense variant +1 more)	FLT3-related disorder	GLikely benign
Select item 2623780	NM_004119.3(FLT3):c.1290G>C (p.Met430Ile)	FLT3 (M430I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605536	NM_004119.3(FLT3):c.1382C>T (p.Ser461Phe)	FLT3 (S461F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604418	NM_004119.3(FLT3):c.1622A>G (p.Asn541Ser)	FLT3 (N541S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2601724	NM_004119.3(FLT3):c.916A>C (p.Asn306His)	FLT3 (N306H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2572500	NM_004119.3(FLT3):c.2533A>G (p.Arg845Gly)	FLT3 (R845G)	Single nucleotide variant (missense variant +1 more)	Acute myeloid leukemia	GLikely pathogenic
Select item 2568692	NM_004119.3(FLT3):c.823G>A (p.Val275Ile)	FLT3 (V275I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537176	NM_004119.3(FLT3):c.843C>G (p.Phe281Leu)	FLT3 (F281L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2533710	NM_004119.3(FLT3):c.1082T>C (p.Ile361Thr)	FLT3 (I361T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532313	NM_004119.3(FLT3):c.2716T>C (p.Phe906Leu)	FLT3 (F906L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493007	NM_004119.3(FLT3):c.884G>A (p.Gly295Asp)	FLT3 (G295D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485171	NM_004119.3(FLT3):c.1286A>C (p.Lys429Thr)	FLT3 (K429T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474795	NM_004119.3(FLT3):c.2642T>C (p.Ile881Thr)	FLT3 (I881T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397815	NM_004119.3(FLT3):c.2881C>T (p.Arg961Cys)	FLT3 (R961C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2363939	NM_004119.3(FLT3):c.524A>G (p.Lys175Arg)	FLT3 (K175R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335821	NM_004119.3(FLT3):c.1512T>A (p.Ser504Arg)	FLT3 (S504R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331709	NM_004119.3(FLT3):c.2014G>A (p.Glu672Lys)	FLT3 (E672K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328288	NM_004119.3(FLT3):c.871G>C (p.Ala291Pro)	FLT3 (A291P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314361	NM_004119.3(FLT3):c.2882G>A (p.Arg961His)	FLT3 (R961H)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2307337	NM_004119.3(FLT3):c.1067G>A (p.Ser356Asn)	FLT3 (S356N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295190	NM_004119.3(FLT3):c.2616G>C (p.Trp872Cys)	FLT3 (W872C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2282729	NM_004119.3(FLT3):c.2482T>C (p.Cys828Arg)	FLT3 (C828R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273320	NM_004119.3(FLT3):c.770T>G (p.Leu257Trp)	FLT3 (L257W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2253219	NM_004119.3(FLT3):c.113T>A (p.Ile38Asn)	FLT3 (I38N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251121	NM_004119.3(FLT3):c.1478G>T (p.Gly493Val)	FLT3 (G493V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249906	NM_004119.3(FLT3):c.251A>G (p.Asp84Gly)	FLT3 (D84G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231893	NM_004119.3(FLT3):c.2126A>C (p.Lys709Thr)	FLT3 (K709T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209537	NM_004119.3(FLT3):c.950T>A (p.Val317Glu)	FLT3 (V317E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2064171	NM_004119.3(FLT3):c.2554G>A (p.Val852Ile)	FLT3 (V852I)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 1711135	t(13;14)(q12.2;q32.12)	TRIP11, FLT3	Translocation	Myeloid neoplasm	GPathogenic
Select item 1710518	GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3	B3GLCT, HS6ST3 +332 more	Copy number gain	not provided	GPathogenic
Select item 1703573	GRCh37/hg19 13p13-q34(chr13:1-115169878)	ABCC4, ABHD13 +332 more	Copy number gain	Complete trisomy 13 syndrome	GPathogenic
Select item 1527750	GRCh37/hg19 13q11-34(chr13:19436286-115107733)	ABCC4, ABHD13 +332 more	Copy number gain	not specified	GPathogenic
Select item 1527749	GRCh37/hg19 13q11-34(chr13:19436286-114981726)	VPS36, VWA8 +329 more	Copy number gain	not specified	GPathogenic
Select item 1341081	GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	not provided	GPathogenic
Select item 1321996	GRCh37/hg19 13p13-q34(chr13:1-115169878)x3	DACH1, IRS2 +332 more	Copy number gain	See cases	GPathogenic
Select item 1291994	NM_004119.3(FLT3):c.1310-3T>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1291612	NM_004119.3(FLT3):c.2053+23A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288964	NM_004119.3(FLT3):c.1597+236A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288512	NM_004119.3(FLT3):c.2053+321C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287572	NM_004119.3(FLT3):c.44-136A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287287	NM_004119.3(FLT3):c.615-297C>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287159	NM_004119.3(FLT3):c.369-326A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286972	NM_004119.3(FLT3):c.2418+38_2418+39del	FLT3	Deletion (intron variant)	not provided	GBenign
Select item 1286964	NM_004119.3(FLT3):c.2418+300G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286527	NM_004119.3(FLT3):c.1205+224C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286009	NM_004119.3(FLT3):c.1419-15T>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283726	NM_004119.3(FLT3):c.2654-102G>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283693	NM_004119.3(FLT3):c.1206-294T>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282410	NM_004119.3(FLT3):c.2291-335dup	FLT3	Duplication (intron variant)	not provided	GBenign
Select item 1281899	NM_004119.3(FLT3):c.1205+56C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280714	NM_004119.3(FLT3):c.1418+75A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1280165	NM_004119.3(FLT3):c.288C>T (p.Asp96=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1279467	NM_004119.3(FLT3):c.2290+173A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279150	NM_004119.3(FLT3):c.44-256G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278209	NM_004119.3(FLT3):c.615-72G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277569	NM_004119.3(FLT3):c.368+189C>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277163	NM_004119.3(FLT3):c.2654-116G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1276512	NM_004119.3(FLT3):c.166-148G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274485	NM_004119.3(FLT3):c.1310-175A>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274386	NM_004119.3(FLT3):c.615-184G>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273290	NM_004119.3(FLT3):c.2053+67CT[10]	FLT3	Microsatellite (intron variant)	not provided	GBenign
Select item 1270594	NM_004119.3(FLT3):c.2291-225C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270334	NM_004119.3(FLT3):c.1942+314C>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1269860	NM_004119.3(FLT3):c.1309+106del	FLT3	Deletion (intron variant)	not provided	GBenign
Select item 1268770	NM_004119.3(FLT3):c.743-36dup	FLT3	Duplication (intron variant)	not provided	GBenign
Select item 1265822	NM_004119.3(FLT3):c.1942+35A>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265575	NM_004119.3(FLT3):c.1206-285T>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263811	NM_004119.3(FLT3):c.166-106G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263141	NM_004119.3(FLT3):c.883-25C>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260309	NM_004119.3(FLT3):c.165+118G>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257200	NM_004119.3(FLT3):c.2053+67CT[9]	FLT3	Microsatellite (intron variant)	not provided	GBenign
Select item 1256865	NM_004119.3(FLT3):c.2653+65G>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256816	NM_004119.3(FLT3):c.485-214G>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253763	NM_004119.3(FLT3):c.2419-187G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253749	NM_004119.3(FLT3):c.1419-36T>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1253421	NM_004119.3(FLT3):c.882+13G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1252193	NM_004119.3(FLT3):c.615-15C>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251597	NM_004119.3(FLT3):c.20A>G (p.Asp7Gly)	FLT3, LOC130009448 (D7G)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1246196	NM_004119.3(FLT3):c.1309+345G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245510	NM_004119.3(FLT3):c.2541+58A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign

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