Related gene-specific medical variations for Gene (Select 643394) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3322255	NM_001040433.2(SPINK9):c.18A>G (p.Ile6Met)	FBXO38-DT, SPINK9 (I6M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322254	NM_001040433.2(SPINK9):c.14C>G (p.Ala5Gly)	FBXO38-DT, SPINK9 (A5G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3169162	NM_001040433.2(SPINK9):c.65G>A (p.Cys22Tyr)	FBXO38-DT, SPINK9 (C22Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3169161	NM_001040433.2(SPINK9):c.50T>C (p.Met17Thr)	FBXO38-DT, SPINK9 (M17T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3169160	NM_001040433.2(SPINK9):c.34C>A (p.Leu12Met)	FBXO38-DT, SPINK9 (L12M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480032	NM_001040433.2(SPINK9):c.38C>T (p.Thr13Ile)	FBXO38-DT, SPINK9 (T13I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275367	NM_001040433.2(SPINK9):c.163G>A (p.Gly55Arg)	FBXO38-DT, SPINK9 (G55R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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