"GeneDx"[submitter] AND "FLT3"[gene] - ClinVar

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Search results

Items: 77

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59853	GRCh38/hg38 13q11-13.3(chr13:18676442-37656039)x3	LOC130009419, LOC130009420 +567 more	Copy number gain	See cases	GPathogenic
Select item 59861	GRCh38/hg38 13q12.11-12.3(chr13:18958091-31090460)x3	LOC130009490, LOC130009491 +416 more	Copy number gain	See cases	GPathogenic
Select item 145957	GRCh38/hg38 13q12.13-12.3(chr13:26965244-30097858)x3	CDX2, FLT1 +123 more	Copy number gain	See cases	GLikely pathogenic
Select item 1178009	NM_004119.3(FLT3):c.2958G>A (p.Pro986=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 1243109	NM_004119.3(FLT3):c.2753+27G>A	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 1277163	NM_004119.3(FLT3):c.2654-116G>A	FLT3	Single nucleotide variant (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 1231363	NM_004119.3(FLT3):c.2542-304G>C	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
Select item 1253763	NM_004119.3(FLT3):c.2419-187G>A	FLT3	Single nucleotide variant (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 1230721	NM_004119.3(FLT3):c.2418+128G>A	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 1270594	NM_004119.3(FLT3):c.2291-225C>T	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 1279467	NM_004119.3(FLT3):c.2290+173A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228322	NM_004119.3(FLT3):c.2054-243G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224230	NM_004119.3(FLT3):c.2054-273A>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 1273290	NM_004119.3(FLT3):c.2053+67CT[10]	FLT3	Microsatellite (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 1221647	NM_004119.3(FLT3):c.2053+59G>A	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 1241612	NM_004119.3(FLT3):c.1943-179A>G	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 1232565	NM_004119.3(FLT3):c.1942+108A>T	FLT3	Single nucleotide variant (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 1226610	NM_004119.3(FLT3):c.1683A>G (p.Leu561=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 134434	NM_004119.3(FLT3):c.1669G>A (p.Val557Ile)	FLT3 (V557I)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1235360	NM_004119.3(FLT3):c.1598-267A>C	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 1226990	NM_004119.3(FLT3):c.1597+233C>G	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 1253749	NM_004119.3(FLT3):c.1419-36T>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224799	NM_004119.3(FLT3):c.1418+81A>G	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 1291994	NM_004119.3(FLT3):c.1310-3T>C	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 1246196	NM_004119.3(FLT3):c.1309+345G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1175588	NM_004119.3(FLT3):c.1309+173T>C	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 1178254	NM_004119.3(FLT3):c.1206-205A>G	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228527	NM_004119.3(FLT3):c.1206-244G>A	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 1283693	NM_004119.3(FLT3):c.1206-294T>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227575	NM_004119.3(FLT3):c.1206-313C>T	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 1281899	NM_004119.3(FLT3):c.1205+56C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 134451	NM_004119.3(FLT3):c.970G>A (p.Asp324Asn)	FLT3 (D324N)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GLikely benign
Select item 1263141	NM_004119.3(FLT3):c.883-25C>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 1268770	NM_004119.3(FLT3):c.743-36dup	FLT3	Duplication (intron variant)	not provided	GBenign
Select item 134447	NM_004119.3(FLT3):c.680C>T (p.Thr227Met)	FLT3 (T227M)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign OBenign
Select item 1252193	NM_004119.3(FLT3):c.615-15C>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 1274386	NM_004119.3(FLT3):c.615-184G>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228796	NM_004119.3(FLT3):c.615-228G>A	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 1256816	NM_004119.3(FLT3):c.485-214G>C	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226785	NM_004119.3(FLT3):c.484+81C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229279	NM_004119.3(FLT3):c.369-269T>C	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 1235679	NM_004119.3(FLT3):c.369-343G>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 1280165	NM_004119.3(FLT3):c.288C>T (p.Asp96=)	FLT3	Single nucleotide variant (synonymous variant +1 more)	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 1276512	NM_004119.3(FLT3):c.166-148G>A	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234126	NM_004119.3(FLT3):c.166-240C>T	FLT3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232922	NM_004119.3(FLT3):c.165+269C>G	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 1226703	NM_004119.3(FLT3):c.44-81T>C	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 1279150	NM_004119.3(FLT3):c.44-256G>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 1233914	NC_000013.11:g.28100741C>T	FLT3, LOC130009449	Single nucleotide variant	not provided	GBenign
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic

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Items: 77