"Ambry Genetics"[submitter] AND "FOXM1"[gene] - ClinVar

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Items: 54

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2535444	NM_021953.4(FOXM1):c.2249C>T (p.Pro750Leu)	FOXM1, ITFG2 (P691L +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456131	NM_021953.4(FOXM1):c.2147G>A (p.Arg716His)	FOXM1, ITFG2 (R658H +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597679	NM_021953.4(FOXM1):c.2144A>G (p.Asn715Ser)	FOXM1, ITFG2 (N714S +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2388150	NM_021953.4(FOXM1):c.2114C>T (p.Pro705Leu)	FOXM1, ITFG2 (P691L +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394995	NM_021953.4(FOXM1):c.2036C>T (p.Ser679Leu)	FOXM1, ITFG2 (S679L +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213346	NM_021953.4(FOXM1):c.1975C>T (p.Leu659Phe)	FOXM1, ITFG2 (L418F +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262751	NM_021953.4(FOXM1):c.1945C>G (p.Pro649Ala)	FOXM1, ITFG2 (P633A +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096500	NM_021953.4(FOXM1):c.1915C>G (p.Pro639Ala)	FOXM1, ITFG2 (P581A +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410190	NM_021953.4(FOXM1):c.1915C>T (p.Pro639Ser)	FOXM1, ITFG2 (P383S +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249446	NM_021953.4(FOXM1):c.1826C>T (p.Ser609Phe)	FOXM1, ITFG2 (S550F +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622032	NM_021953.4(FOXM1):c.1819C>A (p.Pro607Thr)	FOXM1, ITFG2 (P351T +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096499	NM_021953.4(FOXM1):c.1817T>C (p.Leu606Pro)	FOXM1, ITFG2 (L590P +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335169	NM_021953.4(FOXM1):c.1814C>T (p.Thr605Met)	FOXM1, ITFG2 (T547M +14 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2218395	NM_021953.4(FOXM1):c.1799C>T (p.Thr600Ile)	FOXM1, ITFG2 (T584I +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279625	NM_021953.4(FOXM1):c.1738G>A (p.Asp580Asn)	FOXM1, ITFG2 (D619N +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362728	NM_021953.4(FOXM1):c.1717G>A (p.Ala573Thr)	FOXM1, ITFG2 (A515T +14 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3096498	NM_021953.4(FOXM1):c.1708C>T (p.Arg570Cys)	FOXM1, ITFG2 (R329C +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096497	NM_021953.4(FOXM1):c.1701T>A (p.Ser567Arg)	FOXM1, ITFG2 (S311R +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211491	NM_021953.4(FOXM1):c.1673C>T (p.Pro558Leu)	FOXM1, ITFG2 (P302L +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233833	NM_021953.4(FOXM1):c.1669G>A (p.Glu557Lys)	FOXM1, ITFG2 (E499K +14 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487565	NM_021953.4(FOXM1):c.1661G>T (p.Cys554Phe)	FOXM1, ITFG2 (C313F +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512160	NM_021953.4(FOXM1):c.1642C>G (p.Gln548Glu)	FOXM1, ITFG2 (Q292E +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519093	NM_021953.4(FOXM1):c.1633C>T (p.Arg545Trp)	FOXM1, ITFG2 (R567W +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480526	NM_021953.4(FOXM1):c.1633C>G (p.Arg545Gly)	FOXM1, ITFG2 (R531G +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609663	NM_021953.4(FOXM1):c.1628G>A (p.Arg543Gln)	FOXM1, ITFG2 (R485Q +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096496	NM_021953.4(FOXM1):c.1627C>T (p.Arg543Trp)	FOXM1, ITFG2 (R565W +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096495	NM_021953.4(FOXM1):c.1583C>T (p.Ser528Leu)	FOXM1, ITFG2 (S470L +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096494	NM_021953.4(FOXM1):c.1517C>A (p.Ser506Tyr)	FOXM1, ITFG2 (S447Y +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096493	NM_021953.4(FOXM1):c.1495T>C (p.Ser499Pro)	FOXM1, ITFG2 (S498P +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2619736	NM_021953.4(FOXM1):c.1421C>T (p.Ala474Val)	FOXM1, ITFG2 (A233V +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2275544	NM_021953.4(FOXM1):c.1373C>T (p.Thr458Ile)	FOXM1, ITFG2 (T202I +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464210	NM_021953.4(FOXM1):c.1339G>A (p.Gly447Arg)	FOXM1, ITFG2 (G191R +14 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3096492	NM_021953.4(FOXM1):c.1331T>C (p.Leu444Pro)	FOXM1, ITFG2 (L203P +14 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2210820	NM_021953.4(FOXM1):c.1295C>G (p.Pro432Arg)	FOXM1, ITFG2 (P417R +14 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540224	NM_021953.4(FOXM1):c.1252C>T (p.Arg418Cys)	FOXM1 (R360C +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520218	NM_021953.4(FOXM1):c.1235G>A (p.Arg412His)	FOXM1 (R171H +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299748	NM_021953.4(FOXM1):c.1234C>T (p.Arg412Cys)	FOXM1 (P432L +11 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096490	NM_021953.4(FOXM1):c.1226A>G (p.Glu409Gly)	FOXM1 (E350G +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487883	NM_021953.4(FOXM1):c.1181C>T (p.Ser394Leu)	FOXM1 (S336L +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2592239	NM_021953.4(FOXM1):c.1049G>A (p.Arg350His)	FOXM1 (R351H +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2516304	NM_021953.4(FOXM1):c.766C>T (p.Arg256Cys)	FOXM1 (R255C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096505	NM_021953.4(FOXM1):c.680C>T (p.Ala227Val)	FOXM1 (A226V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306979	NM_021953.4(FOXM1):c.668C>T (p.Ser223Leu)	FOXM1 (S223L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357822	NM_021953.4(FOXM1):c.611T>C (p.Met204Thr)	FOXM1 (M204T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337796	NM_021953.4(FOXM1):c.599T>C (p.Ile200Thr)	FOXM1 (I200T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096504	NM_021953.4(FOXM1):c.593G>A (p.Arg198His)	FOXM1 (R198H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317046	NM_021953.4(FOXM1):c.497C>A (p.Thr166Asn)	FOXM1 (T166N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096503	NM_021953.4(FOXM1):c.491G>A (p.Arg164Gln)	FOXM1 (R164Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096501	NM_021953.4(FOXM1):c.451A>C (p.Asn151His)	FOXM1 (N151H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380426	NM_021953.4(FOXM1):c.425G>A (p.Gly142Glu)	FOXM1 (G142E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287163	NM_021953.4(FOXM1):c.365G>A (p.Arg122Gln)	FOXM1 (R122Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2267760	NM_021953.4(FOXM1):c.349C>A (p.Gln117Lys)	FOXM1 (Q117K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317630	NM_021953.4(FOXM1):c.203C>A (p.Pro68His)	FOXM1 (P68H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096489	NM_021953.4(FOXM1):c.121T>G (p.Ser41Ala)	FOXM1 (S41A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 54