"Ambry Genetics"[submitter] AND "ASCL4"[gene] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2528145	NM_203436.3(ASCL4):c.36G>T (p.Leu12Phe)	ASCL4 (L12F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130285	NM_203436.3(ASCL4):c.67G>C (p.Val23Leu)	ASCL4 (V23L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130286	NM_203436.3(ASCL4):c.74G>A (p.Gly25Glu)	ASCL4 (G25E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250573	NM_203436.3(ASCL4):c.95G>A (p.Arg32Gln)	ASCL4 (R32Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391469	NM_203436.3(ASCL4):c.151C>T (p.Arg51Cys)	ASCL4 (R51C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325266	NM_203436.3(ASCL4):c.190C>T (p.Pro64Ser)	ASCL4 (P64S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130281	NM_203436.3(ASCL4):c.239G>T (p.Arg80Leu)	ASCL4 (R80L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364484	NM_203436.3(ASCL4):c.275A>G (p.Tyr92Cys)	ASCL4 (Y92C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351101	NM_203436.3(ASCL4):c.298C>A (p.Pro100Thr)	ASCL4 (P100T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130282	NM_203436.3(ASCL4):c.343C>T (p.Arg115Cys)	ASCL4 (R115C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3317910	NM_203436.3(ASCL4):c.353T>C (p.Ile118Thr)	ASCL4 (I118T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230560	NM_203436.3(ASCL4):c.457G>C (p.Gly153Arg)	ASCL4 (G153R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130283	NM_203436.3(ASCL4):c.458G>A (p.Gly153Glu)	ASCL4 (G153E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526045	NM_203436.3(ASCL4):c.467A>G (p.Lys156Arg)	ASCL4 (K156R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130284	NM_203436.3(ASCL4):c.473C>T (p.Ser158Phe)	ASCL4 (S158F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546987	NM_203436.3(ASCL4):c.507G>T (p.Glu169Asp)	ASCL4 (E169D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance