"PreventionGenetics, part of Exact Sciences"[submitter] AND "NKX3-2"[g - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058375	NM_001189.4(NKX3-2):c.906C>T (p.Pro302=)	NKX3-2	Single nucleotide variant (synonymous variant)	NKX3-2-related disorder	GLikely benign
Select item 1439291	NM_001189.4(NKX3-2):c.700C>T (p.Pro234Ser)	NKX3-2 (P234S)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 498600	NM_001189.4(NKX3-2):c.520G>C (p.Val174Leu)	NKX3-2 (V174L)	Single nucleotide variant (missense variant)	NKX3-2-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 726146	NM_001189.4(NKX3-2):c.493G>C (p.Asp165His)	NKX3-2 (D165H)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2061946	NM_001189.4(NKX3-2):c.336G>A (p.Gly112=)	NKX3-2	Single nucleotide variant (synonymous variant)	NKX3-2-related disorder +1 more	GLikely benign
Select item 770899	NM_001189.4(NKX3-2):c.235A>T (p.Thr79Ser)	NKX3-2 (T79S)	Single nucleotide variant (missense variant)	NKX3-2-related disorder +2 more	GBenign/Likely benign
Select item 708518	NM_001189.4(NKX3-2):c.190G>C (p.Gly64Arg)	NKX3-2 (G64R)	Single nucleotide variant (missense variant)	NKX3-2-related disorder +2 more	GBenign/Likely benign
Select item 497718	NM_001189.4(NKX3-2):c.148T>G (p.Cys50Gly)	NKX3-2 (C50G)	Single nucleotide variant (missense variant)	Connective tissue disorder +2 more	GConflicting classifications of pathogenicity
Select item 728738	NM_001189.4(NKX3-2):c.86C>G (p.Ala29Gly)	NKX3-2 (A29G)	Single nucleotide variant (missense variant)	NKX3-2-related disorder +1 more	GBenign/Likely benign