"Ambry Genetics"[submitter] AND "NUTM1"[gene] - ClinVar

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Items: 53

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2239771	NM_001284292.2(NUTM1):c.145G>A (p.Ala49Thr)	NUTM1 (A21T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203346	NM_001284292.2(NUTM1):c.175C>G (p.Leu59Val)	NUTM1 (L49V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269366	NM_001284292.2(NUTM1):c.253C>T (p.Pro85Ser)	NUTM1 (P57S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203332	NM_001284292.2(NUTM1):c.269T>A (p.Met90Lys)	NUTM1 (M80K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203333	NM_001284292.2(NUTM1):c.281T>C (p.Phe94Ser)	NUTM1 (F94S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324671	NM_001284292.2(NUTM1):c.352G>A (p.Val118Ile)	NUTM1 (V90I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275889	NM_001284292.2(NUTM1):c.431C>T (p.Ser144Leu)	NUTM1 (S144L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325877	NM_001284292.2(NUTM1):c.490G>C (p.Ala164Pro)	NUTM1 (A164P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203342	NM_001284292.2(NUTM1):c.527T>G (p.Val176Gly)	NUTM1 (V176G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534865	NM_001284292.2(NUTM1):c.644G>A (p.Gly215Glu)	NUTM1 (G187E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406137	NM_001284292.2(NUTM1):c.676C>G (p.Pro226Ala)	NUTM1 (P216A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363229	NM_001284292.2(NUTM1):c.691C>T (p.Arg231Cys)	NUTM1 (R203C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203343	NM_001284292.2(NUTM1):c.712G>T (p.Val238Phe)	NUTM1 (V228F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459387	NM_001284292.2(NUTM1):c.727C>T (p.Arg243Cys)	NUTM1 (R243C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372820	NM_001284292.2(NUTM1):c.732G>C (p.Gln244His)	NUTM1 (Q234H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371584	NM_001284292.2(NUTM1):c.739C>T (p.Arg247Cys)	NUTM1 (R219C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203344	NM_001284292.2(NUTM1):c.740G>A (p.Arg247His)	NUTM1 (R247H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334253	NM_001284292.2(NUTM1):c.757C>T (p.Arg253Trp)	NUTM1 (R243W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203345	NM_001284292.2(NUTM1):c.910C>T (p.Arg304Trp)	NUTM1 (R304W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351345	NM_001284292.2(NUTM1):c.1046C>T (p.Pro349Leu)	LOC126862098, NUTM1 (P321L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287483	NM_001284292.2(NUTM1):c.1085C>T (p.Pro362Leu)	LOC126862098, NUTM1 (P352L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223735	NM_001284292.2(NUTM1):c.1111G>C (p.Ala371Pro)	LOC126862098, NUTM1 (A361P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203325	NM_001284292.2(NUTM1):c.1118G>A (p.Arg373His)	LOC126862098, NUTM1 (R363H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369371	NM_001284292.2(NUTM1):c.1148C>T (p.Pro383Leu)	LOC126862098, NUTM1 (P373L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238588	NM_001284292.2(NUTM1):c.1171A>G (p.Ile391Val)	LOC126862098, NUTM1 (I381V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263822	NM_001284292.2(NUTM1):c.1237A>T (p.Thr413Ser)	LOC126862098, NUTM1 (T385S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381445	NM_001284292.2(NUTM1):c.1385A>G (p.Gln462Arg)	NUTM1 (Q434R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203326	NM_001284292.2(NUTM1):c.1439T>C (p.Ile480Thr)	NUTM1 (I480T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529912	NM_001284292.2(NUTM1):c.1498A>G (p.Met500Val)	NUTM1 (M472V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203327	NM_001284292.2(NUTM1):c.1576T>C (p.Ser526Pro)	NUTM1 (S498P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203328	NM_001284292.2(NUTM1):c.1678C>T (p.Arg560Trp)	NUTM1 (R560W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203329	NM_001284292.2(NUTM1):c.1691T>G (p.Val564Gly)	NUTM1 (V564G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203330	NM_001284292.2(NUTM1):c.1711G>A (p.Ala571Thr)	NUTM1 (A543T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203331	NM_001284292.2(NUTM1):c.1767C>A (p.Ser589Arg)	NUTM1 (S561R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210981	NM_001284292.2(NUTM1):c.2053G>A (p.Gly685Arg)	NUTM1 (G657R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378095	NM_001284292.2(NUTM1):c.2084G>A (p.Arg695His)	NUTM1 (R685H +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3203334	NM_001284292.2(NUTM1):c.2107G>A (p.Glu703Lys)	NUTM1 (E675K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203335	NM_001284292.2(NUTM1):c.2215G>T (p.Gly739Trp)	NUTM1 (G729W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283186	NM_001284292.2(NUTM1):c.2254C>A (p.Leu752Met)	NUTM1 (L742M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203336	NM_001284292.2(NUTM1):c.2458G>A (p.Val820Ile)	NUTM1 (V792I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203337	NM_001284292.2(NUTM1):c.2476G>C (p.Glu826Gln)	NUTM1 (E826Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203338	NM_001284292.2(NUTM1):c.2569G>A (p.Val857Ile)	NUTM1 (V829I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2274618	NM_001284292.2(NUTM1):c.2600G>A (p.Gly867Asp)	NUTM1 (G839D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307166	NM_001284292.2(NUTM1):c.2662C>T (p.Pro888Ser)	NUTM1 (P860S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239543	NM_001284292.2(NUTM1):c.2717C>T (p.Pro906Leu)	NUTM1 (P878L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203339	NM_001284292.2(NUTM1):c.2761C>T (p.Pro921Ser)	NUTM1 (P893S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495804	NM_001284292.2(NUTM1):c.2914A>G (p.Lys972Glu)	NUTM1 (K944E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373941	NM_001284292.2(NUTM1):c.2918A>C (p.Asn973Thr)	NUTM1 (N973T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3203340	NM_001284292.2(NUTM1):c.3308G>A (p.Arg1103Gln)	NUTM1 (R1075Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2469916	NM_001284292.2(NUTM1):c.3392C>T (p.Ala1131Val)	NUTM1 (A1131V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378571	NM_001284292.2(NUTM1):c.3428G>A (p.Arg1143Lys)	NUTM1 (R1115K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297202	NM_001284292.2(NUTM1):c.3431G>A (p.Arg1144Gln)	NUTM1 (R1116Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348323	NM_001284292.2(NUTM1):c.3472C>T (p.Arg1158Cys)	NUTM1 (R1130C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 53