"Ambry Genetics"[submitter] AND "NKX2-6"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2401689	NM_001136271.3(NKX2-6):c.589G>A (p.Glu197Lys)	NKX2-6 (E197K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3299927	NM_001136271.3(NKX2-6):c.571C>G (p.Arg191Gly)	NKX2-6 (R191G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2309208	NM_001136271.3(NKX2-6):c.479C>G (p.Pro160Arg)	NKX2-6 (P160R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596443	NM_001136271.3(NKX2-6):c.437C>T (p.Ala146Val)	NKX2-6 (A146V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3299926	NM_001136271.3(NKX2-6):c.398G>A (p.Arg133Gln)	NKX2-6 (R133Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2235266	NM_001136271.3(NKX2-6):c.152G>A (p.Arg51Gln)	NKX2-6 (R51Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3299928	NM_001136271.3(NKX2-6):c.100G>A (p.Val34Met)	NKX2-6 (V34M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign

ClinVar