ASCL1[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2558303	NM_004316.4(ASCL1):c.200G>T (p.Arg67Ile)	ASCL1 (R67I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218022	NM_004316.4(ASCL1):c.206C>T (p.Ala69Val)	ASCL1 (A69V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540946	NM_004316.4(ASCL1):c.245C>A (p.Ala82Glu)	ASCL1 (A82E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271007	NM_004316.4(ASCL1):c.291G>A (p.Met97Ile)	ASCL1 (M97I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616464	NM_004316.4(ASCL1):c.416C>T (p.Ala139Val)	ASCL1 (A139V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130273	NM_004316.4(ASCL1):c.525C>A (p.Asp175Glu)	ASCL1 (D175E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130274	NM_004316.4(ASCL1):c.583C>T (p.Pro195Ser)	ASCL1 (P195S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 162758	NM_004316.4(ASCL1):c.627C>G (p.Val209=)	ASCL1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

ClinVar