"Ambry Genetics"[submitter] AND "STMN3"[gene] - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2475133	NM_015894.4(STMN3):c.530A>G (p.Glu177Gly)	STMN3 (E166G +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2317461	NM_015894.4(STMN3):c.467A>C (p.Glu156Ala)	STMN3 (E145A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2460110	NM_015894.4(STMN3):c.457G>T (p.Ala153Ser)	STMN3 (A142S +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2323597	NM_015894.4(STMN3):c.249G>T (p.Glu83Asp)	STMN3 (E72D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2518469	NM_015894.4(STMN3):c.182C>T (p.Pro61Leu)	STMN3 (P61L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2280551	NM_015894.4(STMN3):c.175A>G (p.Lys59Glu)	STMN3 (K48E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2291014	NM_015894.4(STMN3):c.152G>A (p.Gly51Asp)	STMN3 (G40D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2454971	NM_015894.4(STMN3):c.58C>T (p.Leu20Phe)	STMN3 (L20F +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance