Related gene-specific medical variations for Gene (Select 4824) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2608988	NM_006167.4(NKX3-1):c.177G>T (p.Glu59Asp)	LOC130000042, NKX3-1 (E59D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2592445	NM_006167.4(NKX3-1):c.144C>G (p.Ser48Arg)	LOC130000042, NKX3-1 (S48R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2482425	NM_006167.4(NKX3-1):c.10G>A (p.Val4Ile)	LOC130000042, NKX3-1 (V4I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348296	NM_006167.4(NKX3-1):c.167C>G (p.Pro56Arg)	LOC130000042, NKX3-1 (P56R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2293801	NM_006167.4(NKX3-1):c.169G>C (p.Glu57Gln)	LOC130000042, NKX3-1 (E57Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2207091	NM_006167.4(NKX3-1):c.73C>T (p.Pro25Ser)	LOC130000042, NKX3-1 (P25S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2205915	NM_006167.4(NKX3-1):c.122G>T (p.Arg41Leu)	LOC130000042, NKX3-1 (R41L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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