Related gene-specific medical variations for Gene (Select 256646) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2645149	NM_001284292.2(NUTM1):c.1117del (p.Arg373fs)	LOC126862098, NUTM1 (R345fs +2 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2369371	NM_001284292.2(NUTM1):c.1148C>T (p.Pro383Leu)	LOC126862098, NUTM1 (P373L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2351345	NM_001284292.2(NUTM1):c.1046C>T (p.Pro349Leu)	LOC126862098, NUTM1 (P321L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2287483	NM_001284292.2(NUTM1):c.1085C>T (p.Pro362Leu)	LOC126862098, NUTM1 (P352L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2263822	NM_001284292.2(NUTM1):c.1237A>T (p.Thr413Ser)	LOC126862098, NUTM1 (T385S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2238588	NM_001284292.2(NUTM1):c.1171A>G (p.Ile391Val)	LOC126862098, NUTM1 (I381V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2223735	NM_001284292.2(NUTM1):c.1111G>C (p.Ala371Pro)	LOC126862098, NUTM1 (A361P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 585331	der(15)t(5:15)(q23.2;q15.1)	MGA, NUTM1	Translocation	Spindle cell sarcoma	GPathogenic

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