"Ambry Genetics"[submitter] AND "LOC126862098"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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

ClinVar