"Ambry Genetics"[submitter] AND "DLX6"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3082969	NM_005222.4(DLX6):c.37G>A (p.Gly13Ser)	DLX6, DLX6-AS1 (G13S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082966	NM_005222.4(DLX6):c.126G>T (p.Gln42His)	DLX6, DLX6-AS1 (Q42H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372673	NM_005222.4(DLX6):c.208C>T (p.Pro70Ser)	DLX6, DLX6-AS1 (P70S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082967	NM_005222.4(DLX6):c.261C>G (p.His87Gln)	DLX6, DLX6-AS1 (H87Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082968	NM_005222.4(DLX6):c.320C>T (p.Ser107Phe)	DLX6, DLX6-AS1 (S107F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292433	NM_005222.4(DLX6):c.407C>A (p.Ala136Glu)	DLX6, DLX6-AS1 +1 more (A136E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082970	NM_005222.4(DLX6):c.430G>C (p.Asp144His)	DLX6, DLX6-AS1 (D144H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301836	NM_005222.4(DLX6):c.684G>C (p.Gln228His)	DLX6, DLX6-AS1 (Q228H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253883	NM_005222.4(DLX6):c.708C>A (p.Asp236Glu)	DLX6, DLX6-AS1 (D236E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3082971	NM_005222.4(DLX6):c.744G>A (p.Ser248=)	DLX6, DLX6-AS1	Single nucleotide variant (synonymous variant)	not specified	GLikely benign