"Ambry Genetics"[submitter] AND "METTL25"[gene] - ClinVar

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Items: 49

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2606168	NM_032230.3(METTL25):c.5C>T (p.Ala2Val)	CCDC59, METTL25 (A2V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2287789	NM_032230.3(METTL25):c.16C>T (p.Pro6Ser)	CCDC59, METTL25 (P6S)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3125530	NM_032230.3(METTL25):c.37C>G (p.Leu13Val)	CCDC59, METTL25 (L13V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2209868	NM_032230.3(METTL25):c.95C>G (p.Ser32Cys)	CCDC59, METTL25 (S32C)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2266743	NM_032230.3(METTL25):c.125A>G (p.Tyr42Cys)	CCDC59, METTL25 (Y42C)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2610163	NM_032230.3(METTL25):c.128C>T (p.Thr43Ile)	CCDC59, METTL25 (T43I)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3125526	NM_032230.3(METTL25):c.151G>C (p.Val51Leu)	CCDC59, METTL25 (V51L)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2315772	NM_032230.3(METTL25):c.172G>A (p.Val58Met)	CCDC59, METTL25 (V58M)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2594131	NM_032230.3(METTL25):c.181G>T (p.Ala61Ser)	CCDC59, METTL25 (A61S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2305863	NM_032230.3(METTL25):c.182C>G (p.Ala61Gly)	CCDC59, METTL25 (A61G)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2300515	NM_032230.3(METTL25):c.196G>A (p.Ala66Thr)	CCDC59, METTL25 (A66T)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2362388	NM_032230.3(METTL25):c.347C>T (p.Ser116Phe)	METTL25 (S116F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362389	NM_032230.3(METTL25):c.353A>T (p.Gln118Leu)	METTL25 (Q31L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294448	NM_032230.3(METTL25):c.414C>G (p.Asn138Lys)	METTL25 (N86K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2310782	NM_032230.3(METTL25):c.425G>A (p.Gly142Asp)	METTL25 (G142D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3294449	NM_032230.3(METTL25):c.434A>G (p.Gln145Arg)	METTL25 (Q145R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335724	NM_032230.3(METTL25):c.445G>C (p.Glu149Gln)	METTL25 (E62Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532618	NM_032230.3(METTL25):c.493C>A (p.Leu165Met)	METTL25 (L165M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125531	NM_032230.3(METTL25):c.518A>G (p.Tyr173Cys)	METTL25 (Y173C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3125532	NM_032230.3(METTL25):c.550G>A (p.Gly184Ser)	METTL25 (G132S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125533	NM_032230.3(METTL25):c.587A>G (p.Tyr196Cys)	METTL25 (Y196C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331020	NM_032230.3(METTL25):c.598G>T (p.Val200Phe)	METTL25 (V113F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620848	NM_032230.3(METTL25):c.614C>T (p.Ser205Phe)	METTL25 (S153F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2228273	NM_032230.3(METTL25):c.841T>A (p.Phe281Ile)	METTL25 (F194I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294443	NM_032230.3(METTL25):c.940C>T (p.Leu314Phe)	METTL25 (L262F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231544	NM_032230.3(METTL25):c.949C>A (p.Leu317Ile)	METTL25 (L230I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265615	NM_032230.3(METTL25):c.973C>T (p.Pro325Ser)	METTL25 (P238S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294447	NM_032230.3(METTL25):c.1016C>T (p.Ala339Val)	METTL25 (A287V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607448	NM_032230.3(METTL25):c.1037T>C (p.Met346Thr)	METTL25 (M346T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3125523	NM_032230.3(METTL25):c.1082C>T (p.Ser361Phe)	METTL25 (S361F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342093	NM_032230.3(METTL25):c.1196C>T (p.Thr399Ile)	METTL25 (T312I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2288572	NM_032230.3(METTL25):c.1199C>A (p.Ser400Tyr)	METTL25 (S313Y +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215570	NM_032230.3(METTL25):c.1294A>G (p.Lys432Glu)	METTL25 (K345E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125524	NM_032230.3(METTL25):c.1309A>G (p.Met437Val)	METTL25 (M437V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294446	NM_032230.3(METTL25):c.1349G>A (p.Arg450His)	METTL25 (R450H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459521	NM_032230.3(METTL25):c.1384C>T (p.Arg462Trp)	METTL25 (R462W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125525	NM_032230.3(METTL25):c.1430G>A (p.Arg477His)	METTL25 (R390H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607702	NM_032230.3(METTL25):c.1472C>T (p.Thr491Ile)	METTL25 (T491I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228445	NM_032230.3(METTL25):c.1528T>C (p.Tyr510His)	METTL25 (Y510H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2305203	NM_032230.3(METTL25):c.1576C>T (p.Pro526Ser)	METTL25 (P439S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259946	NM_032230.3(METTL25):c.1608G>C (p.Lys536Asn)	METTL25 (K484N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304235	NM_032230.3(METTL25):c.1619G>A (p.Arg540Gln)	METTL25 (R488Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474727	NM_032230.3(METTL25):c.1646T>C (p.Met549Thr)	METTL25 (M462T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215228	NM_032230.3(METTL25):c.1667C>T (p.Pro556Leu)	METTL25 (P556L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294445	NM_032230.3(METTL25):c.1672A>T (p.Ile558Leu)	METTL25 (I506L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125527	NM_032230.3(METTL25):c.1678A>G (p.Thr560Ala)	METTL25 (T508A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2238576	NM_032230.3(METTL25):c.1706A>C (p.Tyr569Ser)	METTL25 (Y482S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125528	NM_032230.3(METTL25):c.1774A>G (p.Arg592Gly)	METTL25 (R540G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3125529	NM_032230.3(METTL25):c.1777T>C (p.Cys593Arg)	METTL25 (C506R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 49